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		<title>Sensors: Chemical Sensors</title>
		<link>http://www.mdpi.com/section/chemicalsensors</link>
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				<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
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	<item rdf:about="http://www.mdpi.com/1424-8220/12/2/1800/">
	<title>Sensors, Vol. 12, Pages 1800-1815: A Platform for Combined DNA and Protein Microarrays Based on Total Internal Reflection Fluorescence</title>
	<link>http://www.mdpi.com/1424-8220/12/2/1800/</link>
	<description>We have developed a novel microarray technology based on total internal reflection fluorescence (TIRF) in combination with DNA and protein bioassays immobilized at the TIRF surface. Unlike conventional microarrays that exhibit reduced signal-to-background ratio, require several stages of incubation, rinsing and stringency control, and measure only end-point results, our TIRF microarray technology provides several orders of magnitude better signal-to-background ratio, performs analysis rapidly in one step, and measures the entire course of association and dissociation kinetics between target DNA and protein molecules and the bioassays. In many practical cases detection of only DNA or protein markers alone does not provide the necessary accuracy for diagnosing a disease or detecting a pathogen. Here we describe TIRF microarrays that detect DNA and protein markers simultaneously, which reduces the probabilities of false responses. Supersensitive and multiplexed TIRF DNA and protein microarray technology may provide a platform for accurate diagnosis or enhanced research studies. Our TIRF microarray system can be mounted on upright or inverted microscopes or interfaced directly with CCD cameras equipped with a single objective, facilitating the development of portable devices. As proof-of-concept we applied TIRF microarrays for detecting molecular markers from Bacillus anthracis, the pathogen responsible for anthrax.</description>
	
	<guid>http://www.mdpi.com/1424-8220/12/2/1800/</guid>
	<pubDate>Thu, 09 Feb 2012 00:00:00 CET</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2012-02-09</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>1800</prism:startingPage>
		<prism:endingPage>1815</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>A Platform for Combined DNA and Protein Microarrays Based on Total Internal Reflection Fluorescence</dc:title>
	<dc:date>2012-02-09</dc:date>
	<dc:identifier>doi: 10.3390/s120201800</dc:identifier>
		<dc:creator>Alexander Asanov</dc:creator>
		<dc:creator>Angélica Zepeda</dc:creator>
		<dc:creator>Luis Vaca</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/12/2/1422/">
	<title>Sensors, Vol. 12, Pages 1422-1436: An Electronic Nose Based on Coated Piezoelectric Quartz Crystals to Certify Ewes’ Cheese and to Discriminate between Cheese Varieties</title>
	<link>http://www.mdpi.com/1424-8220/12/2/1422/</link>
	<description>An electronic nose based on coated piezoelectric quartz crystals was used to distinguish cheese made from ewes’ milk, and to distinguish cheese varieties. Two sensors coated with Nafion and Carbowax could certify half the ewes’ cheese samples, exclude 32 cheeses made from cow’s milk and to classify half of the ewes’ cheese samples as possibly authentic. Two other sensors, coated with polyvinylpyrrolidone and triethanolamine clearly distinguished between Flamengo, Brie, Gruyère and Mozzarella cheeses. Brie cheeses were further separated according to their origin, and Mozzarella grated cheese also appeared clearly separated from non-grated Mozzarella.</description>
	
	<guid>http://www.mdpi.com/1424-8220/12/2/1422/</guid>
	<pubDate>Wed, 01 Feb 2012 00:00:00 CET</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2012-02-01</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>2</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>1422</prism:startingPage>
		<prism:endingPage>1436</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>An Electronic Nose Based on Coated Piezoelectric Quartz Crystals to Certify Ewes’ Cheese and to Discriminate between Cheese Varieties</dc:title>
	<dc:date>2012-02-01</dc:date>
	<dc:identifier>doi: 10.3390/s120201422</dc:identifier>
		<dc:creator>Vânia F. Pais</dc:creator>
		<dc:creator>João A. B. P. Oliveira</dc:creator>
		<dc:creator>Maria Teresa S. R. Gomes</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/12/1/972/">
	<title>Sensors, Vol. 12, Pages 972-986: Prediction of BOD, COD, and Total Nitrogen Concentrations in a Typical Urban River Using a Fluorescence Excitation-Emission Matrix with PARAFAC and UV Absorption Indices</title>
	<link>http://www.mdpi.com/1424-8220/12/1/972/</link>
	<description>The development of a real-time monitoring tool for the estimation of water quality is essential for efficient management of river pollution in urban areas. The Gap River in Korea is a typical urban river, which is affected by the effluent of a wastewater treatment plant (WWTP) and various anthropogenic activities. In this study, fluorescence excitation-emission matrices (EEM) with parallel factor analysis (PARAFAC) and UV absorption values at 220 nm and 254 nm were applied to evaluate the estimation capabilities for biochemical oxygen demand (BOD), chemical oxygen demand (COD), and total nitrogen (TN) concentrations of the river samples. Three components were successfully identified by the PARAFAC modeling from the fluorescence EEM data, in which each fluorophore group represents microbial humic-like (C1), terrestrial humic-like organic substances (C2), and protein-like organic substances (C3), and UV absorption indices (UV220 and UV254), and the score values of the three PARAFAC components were selected as the estimation parameters for the nitrogen and the organic pollution of the river samples. Among the selected indices, UV220, C3 and C1 exhibited the highest correlation coefficients with BOD, COD, and TN concentrations, respectively. Multiple regression analysis using UV220 and C3 demonstrated the enhancement of the prediction capability for TN.</description>
	
	<guid>http://www.mdpi.com/1424-8220/12/1/972/</guid>
	<pubDate>Mon, 16 Jan 2012 00:00:00 CET</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2012-01-16</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>972</prism:startingPage>
		<prism:endingPage>986</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Prediction of BOD, COD, and Total Nitrogen Concentrations in a Typical Urban River Using a Fluorescence Excitation-Emission Matrix with PARAFAC and UV Absorption Indices</dc:title>
	<dc:date>2012-01-16</dc:date>
	<dc:identifier>doi: 10.3390/s120100972</dc:identifier>
		<dc:creator>Jin Hur</dc:creator>
		<dc:creator>Jinwoo Cho</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/12/1/481/">
	<title>Sensors, Vol. 12, Pages 481-488: Measurement of Organic Chemical Refractive Indexes Using an Optical Time-Domain Reflectometer</title>
	<link>http://www.mdpi.com/1424-8220/12/1/481/</link>
	<description>In this investigation, we propose and experimentally demonstrate a method for measuring the refractive index (RI) of liquid organic chemicals. The scheme is based on a single-mode fiber (SMF) sensor and an optical time-domain reflectometer (OTDR). Here, due to the different reflectance (R) between the SMF and organic liquid chemicals, the reflected power level of the backscattering light (BSL) measured by the OTDR would be different. Therefore, we can measure the RI of chemical under test via the measured BSL level. The proposed RI sensor is simple and easy to manipulate, with stable detected signals, and has the potential to be a valuable tool for use in biological and chemical applications.</description>
	
	<guid>http://www.mdpi.com/1424-8220/12/1/481/</guid>
	<pubDate>Thu, 05 Jan 2012 00:00:00 CET</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2012-01-05</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>481</prism:startingPage>
		<prism:endingPage>488</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Measurement of Organic Chemical Refractive Indexes Using an Optical Time-Domain Reflectometer</dc:title>
	<dc:date>2012-01-05</dc:date>
	<dc:identifier>doi: 10.3390/s120100481</dc:identifier>
		<dc:creator>Chien-Hung Yeh</dc:creator>
		<dc:creator>Chi-Wai Chow</dc:creator>
		<dc:creator>Jiun-Yu Sung</dc:creator>
		<dc:creator>Ping-Chun Wu</dc:creator>
		<dc:creator>Wha-Tzong Whang</dc:creator>
		<dc:creator>Fan-Gang Tseng</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/12/1/260/">
	<title>Sensors, Vol. 12, Pages 260-277: Rapid Classification of Hairtail Fish and Pork Freshness Using an Electronic Nose Based on the PCA Method</title>
	<link>http://www.mdpi.com/1424-8220/12/1/260/</link>
	<description>We report a method for building a simple and reproducible electronic nose based on commercially available metal oxide sensors (MOS) to monitor the freshness of hairtail fish and pork stored at 15, 10, and 5 °C. After assembly in the laboratory, the proposed product was tested by a manufacturer. Sample delivery was based on the dynamic headspace method, and two features were extracted from the transient response of each sensor using an unsupervised principal component analysis (PCA) method. The compensation method and pattern recognition based on PCA are discussed in the current paper. PCA compensation can be used for all storage temperatures, however, pattern recognition differs according to storage conditions. Total volatile basic nitrogen (TVBN) and aerobic bacterial counts of the samples were measured simultaneously with the standard indicators of hairtail fish and pork freshness. The PCA models based on TVBN and aerobic bacterial counts were used to classify hairtail fish samples as “fresh” (TVBN ≤ 25 g and microbial counts ≤ 106 cfu/g) or “spoiled” (TVBN ≥ 25 g and microbial counts ≥ 106 cfu/g) and pork samples also as “fresh” (TVBN ≤ 15 g and microbial counts ≤ 106 cfu/g) or “spoiled” (TVBN ≥ 15 g and microbial counts ≥ 106 cfu/g). Good correlation coefficients between the responses of the electronic nose and the TVBN and aerobic bacterial counts of the samples were obtained. For hairtail fish, correlation coefficients were 0.97 and 0.91, and for pork, correlation coefficients were 0.81 and 0.88, respectively. Through laboratory simulation and field application, we were able to determine that the electronic nose could help ensure the shelf life of hairtail fish and pork, especially when an instrument is needed to take measurements rapidly. The results also showed that the electronic nose could analyze the process and level of spoilage for hairtail fish and pork.</description>
	
	<guid>http://www.mdpi.com/1424-8220/12/1/260/</guid>
	<pubDate>Wed, 28 Dec 2011 00:00:00 CET</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-12-28</prism:publicationDate>
	<prism:volume>12</prism:volume>
	<prism:number>1</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>260</prism:startingPage>
		<prism:endingPage>277</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Rapid Classification of Hairtail Fish and Pork Freshness Using an Electronic Nose Based on the PCA Method</dc:title>
	<dc:date>2011-12-28</dc:date>
	<dc:identifier>doi: 10.3390/s120100260</dc:identifier>
		<dc:creator>Xiu-Ying Tian</dc:creator>
		<dc:creator>Qiang Cai</dc:creator>
		<dc:creator>Yong-Ming Zhang</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/12/11157/">
	<title>Sensors, Vol. 11, Pages 11157-11167: Earthworms and Soil Pollutants</title>
	<link>http://www.mdpi.com/1424-8220/11/12/11157/</link>
	<description>Although the toxicity of metal contaminated soils has been assessed with various bioassays, more information is needed about the biochemical responses, which may help to elucidate the mechanisms involved in metal toxicity. We previously reported that the earthworm, Eisenia fetida, accumulates cadmium in its seminal vesicles. The bio-accumulative ability of earthworms is well known, and thus the earthworm could be a useful living organism for the bio-monitoring of soil pollution. In this short review, we describe recent studies concerning the relationship between earthworms and soil pollutants, and discuss the possibility of using the earthworm as a bio-monitoring organism for soil pollution.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/12/11157/</guid>
	<pubDate>Mon, 28 Nov 2011 00:00:00 CET</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-11-28</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>12</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>11157</prism:startingPage>
		<prism:endingPage>11167</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Earthworms and Soil Pollutants</dc:title>
	<dc:date>2011-11-28</dc:date>
	<dc:identifier>doi: 10.3390/s111211157</dc:identifier>
		<dc:creator>Takeshi Hirano</dc:creator>
		<dc:creator>Kazuyoshi Tamae</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/11/10840/">
	<title>Sensors, Vol. 11, Pages 10840-10850: Electrochemical Characterization of Riboflavin-Enhanced Reduction of Trinitrotoluene</title>
	<link>http://www.mdpi.com/1424-8220/11/11/10840/</link>
	<description>There is great interest in understanding trinitrotoluene (TNT) and dinitrotoluene (DNT) contamination, detection and remediation in the environment due to TNT’s negative health effects and security implications. Numerous publications have focused on detecting TNT in groundwater using multiple techniques, including electrochemistry. The main degradation pathway of nitrotoluenes in the environment is reduction, frequently with biological and/or photolytic assistance. Riboflavin has also been noted to aid in TNT remediation in soils and groundwater when exposed to light. This report indicates that adding riboflavin to a TNT or DNT solution enhances redox currents in electrochemical experiments. Here AC voltammetry was performed and peak currents compared with and without riboflavin present. Results indicated that TNT, DNT and riboflavin could be detected using AC voltammetry on modified gold electrodes and the addition of riboflavin affected redox peaks of TNT and DNT. Poised potential experiments indicated that it is possible to enhance reduction of TNT in the presence of riboflavin and light. These results were dramatic enough to explain long term enhancement of bioremediation in environments containing high levels of riboflavin and enhance the limit of detection in electrochemically-based nitrotoluene sensing.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/11/10840/</guid>
	<pubDate>Fri, 18 Nov 2011 00:00:00 CET</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-11-18</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>11</prism:number>
	<prism:section>Communication</prism:section>
	<prism:startingPage>10840</prism:startingPage>
		<prism:endingPage>10850</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Electrochemical Characterization of Riboflavin-Enhanced Reduction of Trinitrotoluene</dc:title>
	<dc:date>2011-11-18</dc:date>
	<dc:identifier>doi: 10.3390/s111110840</dc:identifier>
		<dc:creator>James J. Sumner</dc:creator>
		<dc:creator>Kevin Chu</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/11/10638/">
	<title>Sensors, Vol. 11, Pages 10638-10663: Bio-Sensing of Cadmium(II) Ions Using Staphylococcus aureus</title>
	<link>http://www.mdpi.com/1424-8220/11/11/10638/</link>
	<description>Cadmium, as a hazardous pollutant commonly present in the living environment, represents an important risk to human health due to its undesirable effects (oxidative stress, changes in activities of many enzymes, interactions with biomolecules including DNA and RNA) and consequent potential risk, making its detection very important. New and unique technological and biotechnological approaches for solving this problems are intensely sought. In this study, we used the commonly occurring potential pathogenic microorganism Staphylococcus aureus for the determination of markers which could be used for sensing of cadmium(II) ions. We were focused on monitoring the effects of different cadmium(II) ion concentrations (0, 1.25, 2.5, 5, 10, 15, 25 and 50 µg mL−1) on the growth and energetic metabolism of Staphylococcus aureus. Highly significant changes have been detected in the metabolism of thiol compounds—specifically the protein metallothionein (0.79–26.82 mmol/mg of protein), the enzyme glutathione S-transferase (190–5,827 µmol/min/mg of protein), and sulfhydryl groups (9.6–274.3 µmol cysteine/mg of protein). The ratio of reduced and oxidized glutathione indicated marked oxidative stress. In addition, dramatic changes in urease activity, which is connected with resistance of bacteria, were determined. Further, the effects of cadmium(II) ions on the metabolic pathways of arginine, β-glucosidase, phosphatase, N-acetyl β-D-glucosamine, sucrose, trehalose, mannitol, maltose, lactose, fructose and total proteins were demonstrated. A metabolomic profile of Staphylococcus aureus under cadmium(II) ion treatment conditions was completed seeking data about the possibility of cadmium(II) ion accumulation in cells. The results demonstrate potential in the application of microorganisms as modern biosensor systems based on biological components.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/11/10638/</guid>
	<pubDate>Tue, 08 Nov 2011 00:00:00 CET</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-11-08</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>11</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>10638</prism:startingPage>
		<prism:endingPage>10663</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Bio-Sensing of Cadmium(II) Ions Using Staphylococcus aureus</dc:title>
	<dc:date>2011-11-08</dc:date>
	<dc:identifier>doi: 10.3390/s111110638</dc:identifier>
		<dc:creator>Jiri Sochor</dc:creator>
		<dc:creator>Ondrej Zitka</dc:creator>
		<dc:creator>David Hynek</dc:creator>
		<dc:creator>Eva Jilkova</dc:creator>
		<dc:creator>Ludmila Krejcova</dc:creator>
		<dc:creator>Libuse Trnkova</dc:creator>
		<dc:creator>Vojtech Adam</dc:creator>
		<dc:creator>Jaromir Hubalek</dc:creator>
		<dc:creator>Jindrich Kynicky</dc:creator>
		<dc:creator>Radimir Vrba</dc:creator>
		<dc:creator>Rene Kizek</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/11/10603/">
	<title>Sensors, Vol. 11, Pages 10603-10614: Design of Selective Gas Sensors Using Additive-Loaded In2O3 Hollow Spheres Prepared by Combinatorial Hydrothermal Reactions</title>
	<link>http://www.mdpi.com/1424-8220/11/11/10603/</link>
	<description>A combinatorial hydrothermal reaction has been used to prepare pure and additive (Sb, Cu, Nb, Pd, and Ni)-loaded In2O3 hollow spheres for gas sensor applications. The operation of Pd- and Cu-loaded In2O3 sensors at 371 °C leads to selective H2S detection. Selective detection of CO and NH3 was achieved by the Ni-In2O3 sensor at sensing temperatures of 371 and 440 °C, respectively. The gas responses of six different sensors to NH3, H2S, H2, CO and CH4 produced unique gas sensing patterns that can be used for the artificial recognition of these gases.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/11/10603/</guid>
	<pubDate>Mon, 07 Nov 2011 00:00:00 CET</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-11-07</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>11</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>10603</prism:startingPage>
		<prism:endingPage>10614</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Design of Selective Gas Sensors Using Additive-Loaded In2O3 Hollow Spheres Prepared by Combinatorial Hydrothermal Reactions</dc:title>
	<dc:date>2011-11-07</dc:date>
	<dc:identifier>doi: 10.3390/s111110603</dc:identifier>
		<dc:creator>Sun-Jung Kim</dc:creator>
		<dc:creator>In-Sung Hwang</dc:creator>
		<dc:creator>Yun Chan Kang</dc:creator>
		<dc:creator>Jong-Heun Lee</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/11/10502/">
	<title>Sensors, Vol. 11, Pages 10502-10521: The Effect of Composition of Different Ecotoxicological Test Media on Free and Bioavailable Copper from CuSO4 and CuO Nanoparticles: Comparative Evidence from a Cu-Selective Electrode and a Cu-Biosensor</title>
	<link>http://www.mdpi.com/1424-8220/11/11/10502/</link>
	<description>The analysis of (bio)available copper in complex environmental settings, including biological test media, is a challenging task. In this study, we demonstrated the potential of a recombinant Pseudomonas fluorescens-based biosensor for bioavailability analysis of CuSO4 and CuO nanoparticles (nano-CuO) in seventeen different ecotoxicological and microbiologial test media. In parallel, free Cu in these test media was analysed using Cu-ion selective electrode (Cu-ISE). In the case of CuSO4, both free and bioavailable Cu decreased greatly with increasing concentration of organics and phosphates in the tested media. A good correlation between free and bioavailable Cu was observed (r = 0.854, p &lt; 0.01) indicating that the free Cu content in biological test media may be a reasonably good predictor for the toxicity of CuSO4. As a proof, it was demonstrated that when eleven EC50 values for CuSO4 from different organisms in different test media were normalized for the free Cu in these media, the difference in these EC50 values was decreased from 4 to 1.8 orders of magnitude. Thus, toxicity of CuSO4 to these organisms was attributed to the properties of the test media rather than to inherent differences in sensitivity between the test organisms. Differently from CuSO4, the amount of free and bioavailable Cu in nano-CuO spiked media was not significantly correlated with the concentration of organics in the test media. Thus, the speciation of nano-CuO in toxicological test systems was not only determined by the complexation of Cu ions but also by differential dissolution of nano-CuO in different test conditions leading to a new speciation equilibrium. In addition, a substantial fraction of nano-CuO that was not detectable by Cu-ISE (i.e., not present as free Cu-ions) was bioavailable to Cu-biosensor bacteria. Thus, in environmental hazard analysis of (nano) particulate materials, biosensor analysis may be more informative than other analytical techniques. Our results demonstrate that bacterial Cu-biosensors either in combination with other analytical/speciation techniques or on their own, may serve as a rapid (eco)toxicological screening method.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/11/10502/</guid>
	<pubDate>Thu, 03 Nov 2011 00:00:00 CET</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-11-03</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>11</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>10502</prism:startingPage>
		<prism:endingPage>10521</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>The Effect of Composition of Different Ecotoxicological Test Media on Free and Bioavailable Copper from CuSO4 and CuO Nanoparticles: Comparative Evidence from a Cu-Selective Electrode and a Cu-Biosensor</dc:title>
	<dc:date>2011-11-03</dc:date>
	<dc:identifier>doi: 10.3390/s111110502</dc:identifier>
		<dc:creator>Aleksandr Käkinen</dc:creator>
		<dc:creator>Olesja Bondarenko</dc:creator>
		<dc:creator>Angela Ivask</dc:creator>
		<dc:creator>Anne Kahru</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/11/10166/">
	<title>Sensors, Vol. 11, Pages 10166-10179: Electrocatalytic Oxidation of Ascorbic Acid Using a Poly(aniline-co-m-ferrocenylaniline) Modified Glassy Carbon Electrode</title>
	<link>http://www.mdpi.com/1424-8220/11/11/10166/</link>
	<description>A poly(aniline-co-m-ferrocenylaniline) was successfully synthesized on a glassy carbon electrode (GCE) by electrochemical copolymerization using a scan potential range from −0.3 to +0.9 V (vs. Ag/AgCl) in 0.5 M H2SO4 containing 30% acetonitrile (ACN), 0.1 M aniline (Ani) and 0.005 M m-ferrocenyaniline (m-FcAni). The field emission scanning electron microscope (FESEM) and electrochemical methods were used to characterize the poly(Ani-co-m-FcAni) modified electrode. The poly(Ani-co-m-FcAni)/GCE exhibited excellent electrocatalytic oxidation of ascorbic acid (AA) in citrate buffer solution (CBS, pH 5.0). The anodic peak potential of AA was shifted from +0.55 V at the bare GCE to +0.25 V at the poly(Ani-co-m-FcAni)/GCE with higher current responses than those seen on the bare GCE. The scan number at the 10th cycle was selected as the maximum scan cycle in electrochemical polymerization. The limit of detection (LOD) was estimated to be 2.0 mM based on the signal-to-noise ratio (S/N = 3). The amperometric responses demonstrated an excellent selectivity for AA determination over glucose (Glu) and dopamine (DA).</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/11/10166/</guid>
	<pubDate>Wed, 26 Oct 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-10-26</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>11</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>10166</prism:startingPage>
		<prism:endingPage>10179</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Electrocatalytic Oxidation of Ascorbic Acid Using a Poly(aniline-co-m-ferrocenylaniline) Modified Glassy Carbon Electrode</dc:title>
	<dc:date>2011-10-26</dc:date>
	<dc:identifier>doi: 10.3390/s111110166</dc:identifier>
		<dc:creator>Sanoe Chairam</dc:creator>
		<dc:creator>Worawit Sriraksa</dc:creator>
		<dc:creator>Maliwan Amatatongchai</dc:creator>
		<dc:creator>Ekasith Somsook</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/10/9685/">
	<title>Sensors, Vol. 11, Pages 9685-9699: Design of Highly Sensitive C2H5OH Sensors Using  Self-Assembled ZnO Nanostructures</title>
	<link>http://www.mdpi.com/1424-8220/11/10/9685/</link>
	<description>Various ZnO nanostructures such as porous nanorods and two hierarchical structures consisting of porous nanosheets or crystalline nanorods were prepared by the reaction of mixtures of oleic-acid-dissolved ethanol solutions and aqueous dissolved Zn-precursor solutions in the presence of NaOH. All three ZnO nanostructures showed sensitive and selective detection of C2H5OH. In particular, ultra-high responses (Ra/Rg = ~1,200, Ra: resistance in air, Rg: resistance in gas) to 100 ppm C2H5OH was attained using porous nanorods and hierarchical structures assembled from porous nanosheets, which is one of the highest values reported in the literature. The gas response and linearity of gas sensors were discussed in relation to the size, surface area, and porosity of the nanostructures.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/10/9685/</guid>
	<pubDate>Wed, 12 Oct 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-10-12</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>10</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>9685</prism:startingPage>
		<prism:endingPage>9699</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Design of Highly Sensitive C2H5OH Sensors Using  Self-Assembled ZnO Nanostructures</dc:title>
	<dc:date>2011-10-12</dc:date>
	<dc:identifier>doi: 10.3390/s111009685</dc:identifier>
		<dc:creator>Kang-Min Kim</dc:creator>
		<dc:creator>Hae-Ryong Kim</dc:creator>
		<dc:creator>Kwon-Il Choi</dc:creator>
		<dc:creator>Hyo-Joong Kim</dc:creator>
		<dc:creator>Jong-Heun Lee</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/10/9560/">
	<title>Sensors, Vol. 11, Pages 9560-9572: Photoinduced Electron Transfer Based Ion Sensing within an Optical Fiber</title>
	<link>http://www.mdpi.com/1424-8220/11/10/9560/</link>
	<description>We combine suspended-core microstructured optical fibers with the photoinduced electron transfer (PET) effect to demonstrate a new type of fluorescent optical fiber-dip sensing platform for small volume ion detection. A sensor design based on a simple model PET-fluoroionophore system and small core microstructured optical fiber capable of detecting sodium ions is demonstrated. The performance of the dip sensor operating in a high sodium concentration regime (925 ppm Na+) and for lower sodium concentration environments (18.4 ppm Na+) is explored and future approaches to improving the sensor’s signal stability, sensitivity and selectivity are discussed.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/10/9560/</guid>
	<pubDate>Tue, 11 Oct 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-10-11</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>10</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>9560</prism:startingPage>
		<prism:endingPage>9572</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Photoinduced Electron Transfer Based Ion Sensing within an Optical Fiber</dc:title>
	<dc:date>2011-10-11</dc:date>
	<dc:identifier>doi: 10.3390/s111009560</dc:identifier>
		<dc:creator>Florian V. Englich</dc:creator>
		<dc:creator>Tze Cheung Foo</dc:creator>
		<dc:creator>Andrew C. Richardson</dc:creator>
		<dc:creator>Heike Ebendorff-Heidepriem</dc:creator>
		<dc:creator>Christopher J. Sumby</dc:creator>
		<dc:creator>Tanya M. Monro</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/10/9207/">
	<title>Sensors, Vol. 11, Pages 9207-9216: Synthesis of Nanocrystalline SnOx (x = 1–2) Thin Film Using a Chemical Bath Deposition Method with Improved Deposition Time, Temperature and pH</title>
	<link>http://www.mdpi.com/1424-8220/11/10/9207/</link>
	<description>Nanocrystalline SnOx (x = 1–2) thin films were prepared on glass substrates by a simple chemical bath deposition method. Triethanolamine was used as complexing agent to decrease time and temperature of deposition and shift the pH of the solution to the noncorrosive region. The films were characterized for composition, surface morphology, structure and optical properties. X-ray diffraction analysis confirms that SnOx thin films consist of a polycrystalline structure with an average grain size of 36 nm. Atomic force microscopy studies show a uniform grain distribution without pinholes. The elemental composition was evaluated by energy dispersive X-ray spectroscopy. The average O/Sn atomic percentage ratio is 1.72. Band gap energy and optical transition were determined from optical absorbance data. The film was found to exhibit direct and indirect transitions in the visible spectrum with band gap values of about 3.9 and 3.7 eV, respectively. The optical transmittance in the visible region is 82%. The SnOx nanocrystals exhibit an ultraviolet emission band centered at 392 nm in the vicinity of the band edge, which is attributed to the well-known exciton transition in SnOx. Photosensitivity was detected in the positive region under illumination with white light.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/10/9207/</guid>
	<pubDate>Tue, 27 Sep 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-09-27</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>10</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>9207</prism:startingPage>
		<prism:endingPage>9216</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Synthesis of Nanocrystalline SnOx (x = 1–2) Thin Film Using a Chemical Bath Deposition Method with Improved Deposition Time, Temperature and pH</dc:title>
	<dc:date>2011-09-27</dc:date>
	<dc:identifier>doi: 10.3390/s111009207</dc:identifier>
		<dc:creator>Saeideh Ebrahimiasl</dc:creator>
		<dc:creator>Wan Md. Zin Wan Yunus</dc:creator>
		<dc:creator>Anuar Kassim</dc:creator>
		<dc:creator>Zulkarnain Zainal</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/9/8888/">
	<title>Sensors, Vol. 11, Pages 8888-8909: Reconstruction of Self-Sparse 2D NMR Spectra from Undersampled Data in the Indirect Dimension</title>
	<link>http://www.mdpi.com/1424-8220/11/9/8888/</link>
	<description>Reducing the acquisition time for two-dimensional nuclear magnetic resonance (2D NMR) spectra is important. One way to achieve this goal is reducing the acquired data. In this paper, within the framework of compressed sensing, we proposed to undersample the data in the indirect dimension for a type of self-sparse 2D NMR spectra, that is, only a few meaningful spectral peaks occupy partial locations, while the rest of locations have very small or even no peaks. The spectrum is reconstructed by enforcing its sparsity in an identity matrix domain with ℓp (p = 0.5) norm optimization algorithm. Both theoretical analysis and simulation results show that the proposed method can reduce the reconstruction errors compared with the wavelet-based ℓ1 norm optimization.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/9/8888/</guid>
	<pubDate>Thu, 15 Sep 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-09-15</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>8888</prism:startingPage>
		<prism:endingPage>8909</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Reconstruction of Self-Sparse 2D NMR Spectra from Undersampled Data in the Indirect Dimension</dc:title>
	<dc:date>2011-09-15</dc:date>
	<dc:identifier>doi: 10.3390/s110908888</dc:identifier>
		<dc:creator>Xiaobo Qu</dc:creator>
		<dc:creator>Di Guo</dc:creator>
		<dc:creator>Xue Cao</dc:creator>
		<dc:creator>Shuhui Cai</dc:creator>
		<dc:creator>Zhong Chen</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/9/8813/">
	<title>Sensors, Vol. 11, Pages 8813-8825: Use of a New Ziprasidone-Selective Electrode in Mixed Solvents and Its Application in the Analysis of Pharmaceuticals and Biological Fluids</title>
	<link>http://www.mdpi.com/1424-8220/11/9/8813/</link>
	<description>The construction and characterization of a new ion-selective electrode for the determination of the antipsychotic ziprasidone in mixed solvents is presented. The electrode contains a plasticized polymeric membrane based on a ziprasidone-tetraphenylborate ion-exchanger. The influence of membrane composition on the electrode response towards ziprasidone in hydroalcoholic solutions was studied. The electrode displayed a stable response in a 2:3 (v/v) methanol/water medium from a ziprasidone concentration of 3 × 10−6 M with a fast response time of less than 20 s. The electrode also showed good selectivity towards ziprasidone over common inorganic and organic compounds and several species with pharmacological activity. The electrode was successfully applied to the determination of ziprasidone in pharmaceuticals and human urine and serum.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/9/8813/</guid>
	<pubDate>Tue, 13 Sep 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-09-13</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>8813</prism:startingPage>
		<prism:endingPage>8825</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Use of a New Ziprasidone-Selective Electrode in Mixed Solvents and Its Application in the Analysis of Pharmaceuticals and Biological Fluids</dc:title>
	<dc:date>2011-09-13</dc:date>
	<dc:identifier>doi: 10.3390/s110908813</dc:identifier>
		<dc:creator>Mª Soledad García</dc:creator>
		<dc:creator>Joaquín A. Ortuño</dc:creator>
		<dc:creator>María Cuartero</dc:creator>
		<dc:creator>Mustafa Salem Abuherba</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/9/8769/">
	<title>Sensors, Vol. 11, Pages 8769-8781: Gamma-Ray Sterilization Effects in Silica Nanoparticles/γ-APTES Nanocomposite-Based pH-Sensitive Polysilicon Wire Sensors</title>
	<link>http://www.mdpi.com/1424-8220/11/9/8769/</link>
	<description>In this paper, we report the γ-ray sterilization effects in pH-sensitive polysilicon wire (PSW) sensors using a mixture of 3-aminopropyltriethoxysilane (γ-APTES) and polydimethylsiloxane (PDMS)-treated hydrophobic fumed silica nanoparticles (NPs) as a sensing membrane. pH analyses showed that the γ-ray irradiation-induced sensitivity degradation of the PSW pH sensor covered with γ-APTES/silica NPs nanocomposite (γ-APTES+NPs) could be restored to a condition even better than prior to γ-ray irradiation by 40-min of post-sterilization room-temperature UV annealing. We found that the trapping charges caused by γ-ray sterilization primarily concentrated in the native oxide layer for the pH sensor covered with γ-APTES, but accumulated in the γ-APTES+NPs layer for the γ-APTES+NPs-covered sensor. It is believed that mixing the PDMS-treated silica NPs into g-APTES provides many g-APTES/SiO2 interfaces for the accumulation of trapping charges and for post-sterilization UV oxidation, thus restoring γ-ray-induced sensor degradation. The PDMS-treated silica NPs not only enhance the sensitivity of the pH-sensitive PSW sensors but are also able to withstand the two-step sterilization resulting from γ-ray and UV irradiations. This investigation suggests γ-ray irradiation could be used as a highly-efficient sterilization method for γ-APTES-based pH-sensitive biosensors.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/9/8769/</guid>
	<pubDate>Tue, 13 Sep 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-09-13</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>8769</prism:startingPage>
		<prism:endingPage>8781</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Gamma-Ray Sterilization Effects in Silica Nanoparticles/γ-APTES Nanocomposite-Based pH-Sensitive Polysilicon Wire Sensors</dc:title>
	<dc:date>2011-09-13</dc:date>
	<dc:identifier>doi: 10.3390/s110908769</dc:identifier>
		<dc:creator>Jing-Jenn Lin</dc:creator>
		<dc:creator>Po-Yen Hsu</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/9/8654/">
	<title>Sensors, Vol. 11, Pages 8654-8664: A Surface Plasmon Resonance Sensor for the Detection of Deoxynivalenol Using a Molecularly Imprinted Polymer</title>
	<link>http://www.mdpi.com/1424-8220/11/9/8654/</link>
	<description>The aim of the present work was to investigate the feasibility of applying the molecular imprinting polymer technique to the detection of the mycotoxin deoxynivalenol (DON) using a surface plasmon resonance (SPR) transducer. A molecularly imprinted polypyrrole (MIPPy) film was prepared via electropolymerization of pyrrole onto a bare Au chip in the presence of a template DON molecule. Atomic force microscope SPR analysis showed that the MIPPy film was deposited homogeneously on the Au surface, with a thickness of 5 nm. The MIPPy–SPR sensor exhibited a linear response for the detection of DON in the range of 0.1–100 ng/mL (R2 = 0.988). The selectivity efficiency of the MIPPy film for DON and its acetylated analogs 3-ADON and 15-ADON was 100, 19, and 44%, respectively. The limit of detection for DON with the MIPPy–SPR for a standard solution was estimated at &gt;1 ng/mL. These results suggest that the combination of SPR sensing with a MIPPy film as a synthetic receptor can be used to detect DON.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/9/8654/</guid>
	<pubDate>Mon, 05 Sep 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-09-05</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>8654</prism:startingPage>
		<prism:endingPage>8664</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>A Surface Plasmon Resonance Sensor for the Detection of Deoxynivalenol Using a Molecularly Imprinted Polymer</dc:title>
	<dc:date>2011-09-05</dc:date>
	<dc:identifier>doi: 10.3390/s110908654</dc:identifier>
		<dc:creator>Sung-Wook Choi</dc:creator>
		<dc:creator>Hyun-Joo Chang</dc:creator>
		<dc:creator>Nari Lee</dc:creator>
		<dc:creator>Hyang Sook Chun</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/9/8643/">
	<title>Sensors, Vol. 11, Pages 8643-8653: Ethanol Vapor Sensing Properties of Triangular Silver Nanostructures Based on Localized Surface Plasmon Resonance</title>
	<link>http://www.mdpi.com/1424-8220/11/9/8643/</link>
	<description>A sensitive volatile organic vapor sensor based on the LSPR properties of silver triangular nanoprisms is proposed in this paper. The triangular nanoprisms were fabricated by a nanosphere lithography (NSL) method. They have sharp vertices and edges, and are arranged in an ideal hexangular array. These characteristics ensure that they exhibit an excellent LSPR spectrum and a high sensitivity to the exterior environment changes. The LSPR spectra responding to ethanol vapor and four other volatile organic vapors—acetone, benzene, hexane and propanol—were measured with a UV-vis spectrometer in real time. Compared with the other four vapors, ethanol exhibits the highest sensitivity (~0.1 nm/mg L−1) and the lowest detection limit (~10 mg/L) in the spectral tests. The ethanol vapor test process is also fast (~4 s) and reversible. These insights demonstrate that the triangular nanoprism based nano-sensor can be used in ethanol vapor detection applications.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/9/8643/</guid>
	<pubDate>Mon, 05 Sep 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-09-05</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>8643</prism:startingPage>
		<prism:endingPage>8653</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Ethanol Vapor Sensing Properties of Triangular Silver Nanostructures Based on Localized Surface Plasmon Resonance</dc:title>
	<dc:date>2011-09-05</dc:date>
	<dc:identifier>doi: 10.3390/s110908643</dc:identifier>
		<dc:creator>Wenying Ma</dc:creator>
		<dc:creator>Huan Yang</dc:creator>
		<dc:creator>Weimin Wang</dc:creator>
		<dc:creator>Ping Gao</dc:creator>
		<dc:creator>Jun Yao</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/9/8611/">
	<title>Sensors, Vol. 11, Pages 8611-8625: Conductometric Sensors for Monitoring Degradation of Automotive Engine Oil</title>
	<link>http://www.mdpi.com/1424-8220/11/9/8611/</link>
	<description>Conductometric sensors have been fabricated by applying imprinted polymers as receptors for monitoring engine oil quality. Titania and silica layers are synthesized via the sol-gel technique and used as recognition materials for acidic components present in used lubricating oil. Thin-film gold electrodes forming an interdigitated structure are used as transducers to measure the conductance of polymer coatings. Optimization of layer composition is carried out by varying the precursors, e.g., dimethylaminopropyltrimethoxysilane (DMAPTMS), and aminopropyl-triethoxysilane (APTES). Characterization of these sensitive materials is performed by testing against oil oxidation products, e.g., carbonic acids. The results depict that imprinted aminopropyltriethoxysilane (APTES) polymer is a promising candidate for detecting the age of used lubricating oil. In the next strategy, polyurethane-nanotubes composite as sensitive material is synthesized, producing appreciable differentiation pattern between fresh and used oils at elevated temperature with enhanced sensitivity.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/9/8611/</guid>
	<pubDate>Mon, 05 Sep 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-09-05</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>8611</prism:startingPage>
		<prism:endingPage>8625</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Conductometric Sensors for Monitoring Degradation of Automotive Engine Oil</dc:title>
	<dc:date>2011-09-05</dc:date>
	<dc:identifier>doi: 10.3390/s110908611</dc:identifier>
		<dc:creator>Usman Latif</dc:creator>
		<dc:creator>Franz L. Dickert</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/9/8485/">
	<title>Sensors, Vol. 11, Pages 8485-8496: Wireless Remote Monitoring of Glucose Using a Functionalized ZnO Nanowire Arrays Based Sensor</title>
	<link>http://www.mdpi.com/1424-8220/11/9/8485/</link>
	<description>This paper presents a prototype wireless remote glucose monitoring system interfaced with a ZnO nanowire arrays-based glucose sensor, glucose oxidase enzyme immobilized onto ZnO nanowires in conjunction with a Nafion® membrane coating, which can be effectively applied for the monitoring of glucose levels in diabetics. Global System for Mobile Communications (GSM) services like General Packet Radio Service (GPRS) and Short Message Service (SMS) have been proven to be logical and cost effective methods for gathering data from remote locations. A communication protocol that facilitates remote data collection using SMS has been utilized for monitoring a patient’s sugar levels. In this study, we demonstrate the remote monitoring of the glucose levels with existing GPRS/GSM network infra-structures using our proposed functionalized ZnO nanowire arrays sensors integrated with standard readily available mobile phones. The data can be used for centralized monitoring and other purposes. Such applications can reduce health care costs and allow caregivers to monitor and support to their patients remotely, especially those located in rural areas.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/9/8485/</guid>
	<pubDate>Mon, 29 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-08-29</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Communication</prism:section>
	<prism:startingPage>8485</prism:startingPage>
		<prism:endingPage>8496</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Wireless Remote Monitoring of Glucose Using a Functionalized ZnO Nanowire Arrays Based Sensor</dc:title>
	<dc:date>2011-08-29</dc:date>
	<dc:identifier>doi: 10.3390/s110908485</dc:identifier>
		<dc:creator>Syed M. Usman Ali</dc:creator>
		<dc:creator>Tasuif Aijazi</dc:creator>
		<dc:creator>Kent Axelsson</dc:creator>
		<dc:creator>Omer Nur</dc:creator>
		<dc:creator>Magnus Willander</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/9/8261/">
	<title>Sensors, Vol. 11, Pages 8261-8280: Determination of the NOx Loading of an Automotive Lean NOx Trap by Directly Monitoring the Electrical Properties of the Catalyst Material Itself</title>
	<link>http://www.mdpi.com/1424-8220/11/9/8261/</link>
	<description>Recently, it has been shown that the degree of loading of several types of automotive exhaust aftertreatment devices can be directly monitored in situ and in a contactless way by a microwave-based method. The goal of this study was to clarify whether this method can also be applied to NOx storage and reduction catalysts (lean NOx traps) in order to obtain further knowledge about the reactions occurring in the catalyst and to compare the results with those obtained by wirebound NOx loading sensors. It is shown that both methods are able to detect the different catalyst loading states. However, the sensitivity of the microwave-based method turned out to be small compared to that previously observed for other exhaust aftertreatment devices. This may limit the practical applicability of the microwave-based NOx loading detection in lean NOx traps.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/9/8261/</guid>
	<pubDate>Thu, 25 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-08-25</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>9</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>8261</prism:startingPage>
		<prism:endingPage>8280</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Determination of the NOx Loading of an Automotive Lean NOx Trap by Directly Monitoring the Electrical Properties of the Catalyst Material Itself</dc:title>
	<dc:date>2011-08-25</dc:date>
	<dc:identifier>doi: 10.3390/s110908261</dc:identifier>
		<dc:creator>Peter Fremerey</dc:creator>
		<dc:creator>Sebastian Reiß</dc:creator>
		<dc:creator>Andrea Geupel</dc:creator>
		<dc:creator>Gerhard Fischerauer</dc:creator>
		<dc:creator>Ralf Moos</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/8/8127/">
	<title>Sensors, Vol. 11, Pages 8127-8142: Dual-Functional On-Chip AlGaAs/GaAs Schottky Diode for RF Power Detection and Low-Power Rectenna Applications</title>
	<link>http://www.mdpi.com/1424-8220/11/8/8127/</link>
	<description>A Schottky diode has been designed and fabricated on an n-AlGaAs/GaAs high-electron-mobility-transistor (HEMT) structure. Current-voltage (I-V) measurements show good device rectification, with a Schottky barrier height of 0.4349 eV for Ni/Au metallization. The differences between the Schottky barrier height and the theoretical value (1.443 eV) are due to the fabrication process and smaller contact area. The RF signals up to 1 GHz are rectified well by the fabricated Schottky diode and a stable DC output voltage is obtained. The increment ratio of output voltage vs input power is 0.2 V/dBm for all tested frequencies, which is considered good enough for RF power detection. Power conversion efficiency up to 50% is obtained at frequency of 1 GHz and input power of 20 dBm with series connection between diode and load, which also shows the device’s good potential as a rectenna device with further improvement. The fabricated n-AlGaAs/GaAs Schottky diode thus provides a conduit for breakthrough designs for RF power detectors, as well as ultra-low power on-chip rectenna device technology to be integrated in nanosystems.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/8/8127/</guid>
	<pubDate>Thu, 18 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-08-18</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>8127</prism:startingPage>
		<prism:endingPage>8142</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Dual-Functional On-Chip AlGaAs/GaAs Schottky Diode for RF Power Detection and Low-Power Rectenna Applications</dc:title>
	<dc:date>2011-08-18</dc:date>
	<dc:identifier>doi: 10.3390/s110808127</dc:identifier>
		<dc:creator>Abdul Manaf Hashim</dc:creator>
		<dc:creator>Farahiyah Mustafa</dc:creator>
		<dc:creator>Shaharin Fadzli Abd Rahman</dc:creator>
		<dc:creator>Abdul Rahim Abdul Rahman</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/8/8072/">
	<title>Sensors, Vol. 11, Pages 8072-8084: Sensitivities of Key Parameters in the Preparation of Silver/Silver Chloride Electrodes Used in Harned Cell Measurements of pH</title>
	<link>http://www.mdpi.com/1424-8220/11/8/8072/</link>
	<description>A questionnaire was completed by fourteen world leading national metrology institutes to study the influence of several variables in the preparation of Ag/AgCl electrodes on the accuracy of Harned cell measurements of pH. The performance of each institute in the last decade has been assessed based on their results in eight key comparisons, organized by the Bureau International des Poids et Measures Consultative Committee for Amount of Substance, involving the measurement of pH of phosphate, phthalate, carbonate, borate and tetroxalate buffer solutions. The performance of each laboratory has been correlated to the results of the questionnaire to determine the critical parameters in the preparation of Ag/AgCl electrodes and their sensitivities with respect to the accuracy of pH measurement. This study reveals that the parameters most closely correlated to performance in comparisons are area of electrode wire exposed to the electrolyte, diameter and porosity of the Ag sphere prior to anodisation, amount of Ag converted to AgCl during anodisation, stability times employed for electrodes to reach equilibrium in solution prior to measurement, electrode rejection criteria employed and purity of reagents.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/8/8072/</guid>
	<pubDate>Wed, 17 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-08-17</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>8072</prism:startingPage>
		<prism:endingPage>8084</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Sensitivities of Key Parameters in the Preparation of Silver/Silver Chloride Electrodes Used in Harned Cell Measurements of pH</dc:title>
	<dc:date>2011-08-17</dc:date>
	<dc:identifier>doi: 10.3390/s110808072</dc:identifier>
		<dc:creator>Paul J. Brewer</dc:creator>
		<dc:creator>Daniela Stoica</dc:creator>
		<dc:creator>Richard J. C. Brown</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/8/7865/">
	<title>Sensors, Vol. 11, Pages 7865-7878: LuxCDABE—Transformed Constitutively Bioluminescent Escherichia coli for Toxicity Screening: Comparison with Naturally Luminous Vibrio fischeri</title>
	<link>http://www.mdpi.com/1424-8220/11/8/7865/</link>
	<description>We show that in vitro toxicity assay based on inhibition of the bioluminescence of recombinant Escherichia coli encoding thermostable luciferase from Photorhabdus luminescens is a versatile alternative to Vibrio fischeri MicrotoxTM test. Performance of two luxCDABE-transformed E. coli MC1061 constructs (pDNlux) and (pSLlux) otherwise identical, but having 100-fold different background luminescence was compared with the performance of V. fischeri. The microplate luminometer and a kinetic Flash-Assay test format was used that differently from Microtox test is also applicable for high throughput analysis. Toxic effects (30-s till 30-min EC50) of four heavy metals (Zn, Cd, Hg, Cu) and three organic chemicals (aniline, 3,5-dichloroaniline and 3,5-dichlorophenol) were studied. Both E. coli strains had comparable sensitivity and the respective 30-min EC50 values highly correlated (log-log R2 = 0.99; p &lt; 0.01) showing that the sensitivity of the recombinant bacteria towards chemicals analyzed did not depend on the bioluminescence level of the recombinant cells. The most toxic chemical for all used bacterial strains (E. coli, V. fischeri) was mercury whereas the lowest EC50 values for Hg (0.04–0.05 mg/L) and highest EC50 values for aniline (1,300–1,700 mg/L) were observed for E. coli strains. Despite of that, toxicity results obtained with both E. coli strains (pSLlux and pDNlux) significantly correlated with V. fischeri results (log-log R2 = 0.70/0.75; p &lt; 0.05/0.01). The use of amino acids (0.25%) and glucose (0.05%)-supplemented M9 medium instead of leucine-supplemented saline significantly (p &lt; 0.05) reduced the apparent toxicity of heavy metals to both E. coli strains up to three orders of magnitude, but had little or no complexing effect on organic compounds. Thus, P. luminescens luxCDABE-transformed E. coli strains can be successfully used for the acute toxicity screening of various types of organic chemicals and heavy metals and can replace V. fischeri in certain cases where the thermostability of luciferase &gt;30 °C is crucial. The kinetic Flash Assay test format of the bioluminescence inhibition assay facilitates high throughput analysis. The assay medium, especially in case of testing heavy metals should be a compromise: optimal for the viability/luminescence of the recombinant test strain and of minimum complexing potential.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/8/7865/</guid>
	<pubDate>Thu, 11 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-08-11</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>7865</prism:startingPage>
		<prism:endingPage>7878</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>LuxCDABE—Transformed Constitutively Bioluminescent Escherichia coli for Toxicity Screening: Comparison with Naturally Luminous Vibrio fischeri</dc:title>
	<dc:date>2011-08-11</dc:date>
	<dc:identifier>doi: 10.3390/s110807865</dc:identifier>
		<dc:creator>Imbi Kurvet</dc:creator>
		<dc:creator>Angela Ivask</dc:creator>
		<dc:creator>Olesja Bondarenko</dc:creator>
		<dc:creator>Mariliis Sihtmäe</dc:creator>
		<dc:creator>Anne Kahru</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/8/7763/">
	<title>Sensors, Vol. 11, Pages 7763-7772: A Single-Walled Carbon Nanotube Network Gas Sensing Device</title>
	<link>http://www.mdpi.com/1424-8220/11/8/7763/</link>
	<description>The goal of this research was to develop a chemical gas sensing device based on single-walled carbon nanotube (SWCNT) networks. The SWCNT networks are synthesized on Al2O3-deposted SiO2/Si substrates with 10 nm-thick Fe as the catalyst precursor layer using microwave plasma chemical vapor deposition (MPCVD). The development of interconnected SWCNT networks can be exploited to recognize the identities of different chemical gases by the strength of their particular surface adsorptive and desorptive responses to various types of chemical vapors. The physical responses on the surface of the SWCNT networks cause superficial changes in the electric charge that can be converted into electronic signals for identification. In this study, we tested NO2 and NH3 vapors at ppm levels at room temperature with our self-made gas sensing device, which was able to obtain responses to sensitivity changes with a concentration of 10 ppm for NO2 and 24 ppm for NH3.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/8/7763/</guid>
	<pubDate>Mon, 08 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-08-08</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>7763</prism:startingPage>
		<prism:endingPage>7772</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>A Single-Walled Carbon Nanotube Network Gas Sensing Device</dc:title>
	<dc:date>2011-08-08</dc:date>
	<dc:identifier>doi: 10.3390/s110807763</dc:identifier>
		<dc:creator>Li-Chun Wang</dc:creator>
		<dc:creator>Kea-Tiong Tang</dc:creator>
		<dc:creator>I-Ju Teng</dc:creator>
		<dc:creator>Cheng-Tzu Kuo</dc:creator>
		<dc:creator>Cheng-Long Ho</dc:creator>
		<dc:creator>Han-Wen Kuo</dc:creator>
		<dc:creator>Tseng-Hsiung Su</dc:creator>
		<dc:creator>Shang-Ren Yang</dc:creator>
		<dc:creator>Gia-Nan Shi</dc:creator>
		<dc:creator>Chang-Ping Chang</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/8/7736/">
	<title>Sensors, Vol. 11, Pages 7736-7748: Planar Zeolite Film-Based Potentiometric Gas Sensors Manufactured by a Combined Thick-Film and Electroplating Technique</title>
	<link>http://www.mdpi.com/1424-8220/11/8/7736/</link>
	<description>Zeolites are promising materials in the field of gas sensors. In this technology-oriented paper, a planar setup for potentiometric hydrocarbon and hydrogen gas sensors using zeolites as ionic sodium conductors is presented, in which the Pt-loaded Na-ZSM-5 zeolite is applied using a thick-film technique between two interdigitated gold electrodes and one of them is selectively covered for the first time by an electroplated chromium oxide film. The influence of the sensor temperature, the type of hydrocarbons, the zeolite film thickness, and the chromium oxide film thickness is investigated. The influence of the zeolite on the sensor response is briefly discussed in the light of studies dealing with zeolites as selectivity-enhancing cover layers.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/8/7736/</guid>
	<pubDate>Fri, 05 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-08-05</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>7736</prism:startingPage>
		<prism:endingPage>7748</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Planar Zeolite Film-Based Potentiometric Gas Sensors Manufactured by a Combined Thick-Film and Electroplating Technique</dc:title>
	<dc:date>2011-08-05</dc:date>
	<dc:identifier>doi: 10.3390/s110807736</dc:identifier>
		<dc:creator>Isabella Marr</dc:creator>
		<dc:creator>Sebastian Reiß</dc:creator>
		<dc:creator>Gunter Hagen</dc:creator>
		<dc:creator>Ralf Moos</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/8/7724/">
	<title>Sensors, Vol. 11, Pages 7724-7735: SnO2/Pt Thin Film Laser Ablated Gas Sensor Array</title>
	<link>http://www.mdpi.com/1424-8220/11/8/7724/</link>
	<description>A gas sensor array was developed in a 10 × 10 mm2 space using Screen Printing and Pulse Laser Ablation Deposition (PLAD) techniques. Heater, electrode, and an insulator interlayer were printed using the screen printing method on an alumina substrate, while tin oxide and platinum films, as sensing and catalyst layers, were deposited on the electrode at room temperature using the PLAD method, respectively. To ablate SnO2 and Pt targets, depositions were achieved by using a 1,064 nm Nd-YAG laser, with a power of 0.7 J/s, at different deposition times of 2, 5 and 10 min, in an atmosphere containing 0.04 mbar (4 kPa) of O2. A range of spectroscopic diffraction and real space imaging techniques, SEM, EDX, XRD, and AFM were used in order to characterize the surface morphology, structure, and composition of the films. Measurement on the array shows sensitivity to some solvent and wood smoke can be achieved with short response and recovery times.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/8/7724/</guid>
	<pubDate>Fri, 05 Aug 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-08-05</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>7724</prism:startingPage>
		<prism:endingPage>7735</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>SnO2/Pt Thin Film Laser Ablated Gas Sensor Array</dc:title>
	<dc:date>2011-08-05</dc:date>
	<dc:identifier>doi: 10.3390/s110807724</dc:identifier>
		<dc:creator>Mohammad Hadi Shahrokh Abadi</dc:creator>
		<dc:creator>Mohd Nizar Hamidon</dc:creator>
		<dc:creator>Abdul Halim Shaari</dc:creator>
		<dc:creator>Norhafizah Abdullah</dc:creator>
		<dc:creator>Rahman Wagiran</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/8/7382/">
	<title>Sensors, Vol. 11, Pages 7382-7394: Estimating the Biodegradability of Treated Sewage Samples Using Synchronous Fluorescence Spectra</title>
	<link>http://www.mdpi.com/1424-8220/11/8/7382/</link>
	<description>Synchronous fluorescence spectra (SFS) and the first derivative spectra of the influent versus the effluent wastewater samples were compared and the use of fluorescence indices is suggested as a means to estimate the biodegradability of the effluent wastewater. Three distinct peaks were identified from the SFS of the effluent wastewater samples. Protein-like fluorescence (PLF) was reduced, whereas fulvic and/or humic-like fluorescence (HLF) were enhanced, suggesting that the two fluorescence characteristics may represent biodegradable and refractory components, respectively. Five fluorescence indices were selected for the biodegradability estimation based on the spectral features changing from the influent to the effluent. Among the selected indices, the relative distribution of PLF to the total fluorescence area of SFS (Index II) exhibited the highest correlation coefficient with total organic carbon (TOC)-based biodegradability, which was even higher than those obtained with the traditional oxygen demand-based parameters. A multiple regression analysis using Index II and the area ratio of PLF to HLF (Index III) demonstrated the enhancement of the correlations from 0.558 to 0.711 for TOC-based biodegradability. The multiple regression equation finally obtained was 0.148 ´ Index II − 4.964 ´ Index III − 0.001 and 0.046 ´ Index II − 1.128 ´ Index III + 0.026. The fluorescence indices proposed here are expected to be utilized for successful development of real-time monitoring using a simple fluorescence sensing device for the biodegradability of treated sewage.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/8/7382/</guid>
	<pubDate>Mon, 25 Jul 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-07-25</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>7382</prism:startingPage>
		<prism:endingPage>7394</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Estimating the Biodegradability of Treated Sewage Samples Using Synchronous Fluorescence Spectra</dc:title>
	<dc:date>2011-07-25</dc:date>
	<dc:identifier>doi: 10.3390/s110807382</dc:identifier>
		<dc:creator>Tien M. Lai</dc:creator>
		<dc:creator>Jae-Ki Shin</dc:creator>
		<dc:creator>Jin Hur</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/8/7327/">
	<title>Sensors, Vol. 11, Pages 7327-7340: Modeling of Slot Waveguide Sensors Based on Polymeric Materials</title>
	<link>http://www.mdpi.com/1424-8220/11/8/7327/</link>
	<description>Slot waveguides are very promising for optical sensing applications because of their peculiar spatial mode profile. In this paper we have carried out a detailed analysis of mode confinement properties in slot waveguides realized in very low refractive index materials. We show that the sensitivity of a slot waveguide is not directly related to the refractive index contrast of high and low materials forming the waveguide. Thus, a careful design of the structures allows the realization of high sensitivity devices even in very low refractive index materials (e.g., polymers) to be achieved. Advantages of low index dielectrics in terms of cost, functionalization and ease of fabrication are discussed while keeping both CMOS compatibility and integrable design schemes. Finally, applications of low index slot waveguides as substitute of bulky fiber capillary sensors or in ring resonator architectures are addressed. Theoretical results of this work are relevant to well established polymer technologies.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/8/7327/</guid>
	<pubDate>Mon, 25 Jul 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-07-25</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>7327</prism:startingPage>
		<prism:endingPage>7340</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Modeling of Slot Waveguide Sensors Based on Polymeric Materials</dc:title>
	<dc:date>2011-07-25</dc:date>
	<dc:identifier>doi: 10.3390/s110807327</dc:identifier>
		<dc:creator>Paolo Bettotti</dc:creator>
		<dc:creator>Alessandro Pitanti</dc:creator>
		<dc:creator>Eveline Rigo</dc:creator>
		<dc:creator>Francesco De Leonardis</dc:creator>
		<dc:creator>Vittorio M. N. Passaro</dc:creator>
		<dc:creator>Lorenzo Pavesi</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/8/7302/">
	<title>Sensors, Vol. 11, Pages 7302-7313: An Optical Test Strip for the Detection of Benzoic Acid in Food</title>
	<link>http://www.mdpi.com/1424-8220/11/8/7302/</link>
	<description>Fabrication of a test strip for detection of benzoic acid was successfully implemented by immobilizing tyrosinase, phenol and 3-methyl-2-benzothiazolinone hydrazone (MBTH) onto filter paper using polystyrene as polymeric support. The sensing scheme was based on the decreasing intensity of the maroon colour of the test strip when introduced into benzoic acid solution. The test strip was characterized using optical fiber reflectance and has maximum reflectance at 375 nm. It has shown a highly reproducible measurement of benzoic acid with a calculated RSD of 0.47% (n = 10). The detection was optimized at pH 7. A linear response of the biosensor was obtained in 100 to 700 ppm of benzoic acid with a detection limit (LOD) of 73.6 ppm. At 1:1 ratio of benzoic acid to interfering substances, the main interfering substance is boric acid. The kinetic analyses show that, the inhibition of benzoic is competitive inhibitor and the inhibition constant (Ki) is 52.9 ppm. The activity of immobilized tyrosinase, phenol, and MBTH in the test strip was fairly sustained during 20 days when stored at 3 °C. The developed test strip was used for detection of benzoic acid in food samples and was observed to have comparable results to the HPLC method, hence the developed test strip can be used as an alternative to HPLC in detecting benzoic acid in food products.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/8/7302/</guid>
	<pubDate>Mon, 25 Jul 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-07-25</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>8</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>7302</prism:startingPage>
		<prism:endingPage>7313</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>An Optical Test Strip for the Detection of Benzoic Acid in Food</dc:title>
	<dc:date>2011-07-25</dc:date>
	<dc:identifier>doi: 10.3390/s110807302</dc:identifier>
		<dc:creator>Hairul Hisham Hamzah</dc:creator>
		<dc:creator>Nor Azah Yusof</dc:creator>
		<dc:creator>Abu Bakar Salleh</dc:creator>
		<dc:creator>Fatimah Abu Bakar</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/7/7127/">
	<title>Sensors, Vol. 11, Pages 7127-7140: Nanocrystalline SnO2:F Thin Films for Liquid Petroleum Gas Sensors</title>
	<link>http://www.mdpi.com/1424-8220/11/7/7127/</link>
	<description>This paper reports the improvement in the sensing performance of nanocrystalline SnO2-based liquid petroleum gas (LPG) sensors by doping with fluorine (F). Un-doped and F-doped tin oxide films were prepared on glass substrates by the dip-coating technique using a layer-by-layer deposition cycle (alternating between dip-coating a thin layer followed by a drying in air after each new layer). The results showed that this technique is superior to the conventional technique for both improving the film thickness uniformity and film transparency. The effect of F concentration on the structural, surface morphological and LPG sensing properties of the SnO2 films was investigated. Atomic Force Microscopy (AFM) and X-ray diffraction pattern measurements showed that the obtained thin films are nanocrystalline SnO2 with nanoscale-textured surfaces. Gas sensing characteristics (sensor response and response/recovery time) of the SnO2:F sensors based on a planar interdigital structure were investigated at different operating temperatures and at different LPG concentrations. The addition of fluorine to SnO2 was found to be advantageous for efficient detection of LPG gases, e.g., F-doped sensors are more stable at a low operating temperature (300 °C) with higher sensor response and faster response/recovery time, compared to un-doped sensor materials. The sensors based on SnO2:F films could detect LPG even at a low level of 25% LEL, showing the possibility of using this transparent material for LPG leak detection.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/7/7127/</guid>
	<pubDate>Mon, 11 Jul 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-07-11</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>7</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>7127</prism:startingPage>
		<prism:endingPage>7140</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Nanocrystalline SnO2:F Thin Films for Liquid Petroleum Gas Sensors</dc:title>
	<dc:date>2011-07-11</dc:date>
	<dc:identifier>doi: 10.3390/s110707127</dc:identifier>
		<dc:creator>Sutichai Chaisitsak</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/7/6893/">
	<title>Sensors, Vol. 11, Pages 6893-6904: Effects of Textural Properties on the Response of a SnO2-Based Gas Sensor for the Detection of Chemical Warfare Agents</title>
	<link>http://www.mdpi.com/1424-8220/11/7/6893/</link>
	<description>The sensing behavior of SnO2-based thick film gas sensors in a flow system in the presence of a very low concentration (ppb level) of chemical agent simulants such as acetonitrile, dipropylene glycol methyl ether (DPGME), dimethyl methylphosphonate (DMMP), and dichloromethane (DCM) was investigated. Commercial SnO2 [SnO2(C)] and nano-SnO2 prepared by the precipitation method [SnO2(P)] were used to prepare the SnO2 sensor in this study. In the case of DCM and acetonitrile, the SnO2(P) sensor showed higher sensor response as compared with the SnO2(C) sensors. In the case of DMMP and DPGME, however, the SnO2(C) sensor showed higher responses than those of the SnO2(P) sensors. In particular, the response of the SnO2(P) sensor increased as the calcination temperature increased from 400 °C to 800 °C. These results can be explained by the fact that the response of the SnO2-based gas sensor depends on the textural properties of tin oxide and the molecular size of the chemical agent simulant in the detection of the simulant gases (0.1–0.5 ppm).</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/7/6893/</guid>
	<pubDate>Fri, 01 Jul 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-07-01</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>7</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>6893</prism:startingPage>
		<prism:endingPage>6904</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Effects of Textural Properties on the Response of a SnO2-Based Gas Sensor for the Detection of Chemical Warfare Agents</dc:title>
	<dc:date>2011-07-01</dc:date>
	<dc:identifier>doi: 10.3390/s110706893</dc:identifier>
		<dc:creator>Soo Chool Lee</dc:creator>
		<dc:creator>Seong Yeol Kim</dc:creator>
		<dc:creator>Woo Suk Lee</dc:creator>
		<dc:creator>Suk Yong Jung</dc:creator>
		<dc:creator>Byung Wook Hwang</dc:creator>
		<dc:creator>Dhanusuraman Ragupathy</dc:creator>
		<dc:creator>Duk Dong Lee</dc:creator>
		<dc:creator>Sang Yeon Lee</dc:creator>
		<dc:creator>Jae Chang Kim</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/7/6509/">
	<title>Sensors, Vol. 11, Pages 6509-6516: A Single Polyaniline Nanofiber Field Effect Transistor and Its Gas Sensing Mechanisms</title>
	<link>http://www.mdpi.com/1424-8220/11/7/6509/</link>
	<description>A single polyaniline nanofiber field effect transistor (FET) gas sensor fabricated by means of electrospinning was investigated to understand its sensing mechanisms and optimize its performance. We studied the morphology, field effect characteristics and gas sensitivity of conductive nanofibers. The fibers showed Schottky and Ohmic contacts based on different electrode materials. Higher applied gate voltage contributes to an increase in gas sensitivity. The nanofiber transistor showed a 7% reversible resistance change to 1 ppm NH3 with 10 V gate voltage. The FET characteristics of the sensor when exposed to different gas concentrations indicate that adsorption of NH3 molecules reduces the carrier mobility in the polyaniline nanofiber. As such, nanofiber-based sensors could be promising for environmental and industrial applications.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/7/6509/</guid>
	<pubDate>Fri, 24 Jun 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-06-24</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>7</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>6509</prism:startingPage>
		<prism:endingPage>6516</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>A Single Polyaniline Nanofiber Field Effect Transistor and Its Gas Sensing Mechanisms</dc:title>
	<dc:date>2011-06-24</dc:date>
	<dc:identifier>doi: 10.3390/s110706509</dc:identifier>
		<dc:creator>Dajing Chen</dc:creator>
		<dc:creator>Sheng Lei</dc:creator>
		<dc:creator>Yuquan Chen</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/6/6425/">
	<title>Sensors, Vol. 11, Pages 6425-6434: Low-Cost Gas Sensors Produced by the Graphite Line-Patterning Technique Applied to Monitoring Banana Ripeness</title>
	<link>http://www.mdpi.com/1424-8220/11/6/6425/</link>
	<description>A low-cost sensor array system for banana ripeness monitoring is presented. The sensors are constructed by employing a graphite line-patterning technique (LPT) to print interdigitated graphite electrodes on tracing paper and then coating the printed area with a thin film of polyaniline (PANI) by in-situ polymerization as the gas-sensitive layer. The PANI layers were used for the detection of volatile organic compounds (VOCs), including ethylene, emitted during ripening. The influence of the various acid dopants, hydrochloric acid (HCl), methanesulfonic acid (MSA), p-toluenesulfonic acid (TSA) and camphorsulfonic acid (CSA), on the electrical properties of the thin film of PANI adsorbed on the electrodes was also studied. The extent of doping of the films was investigated by UV-Vis absorption spectroscopy and tests showed that the type of dopant plays an important role in the performance of these low-cost sensors. The array of three sensors, without the PANI-HCl sensor, was able to produce a distinct pattern of signals, taken as a signature (fingerprint) that can be used to characterize bananas ripeness.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/6/6425/</guid>
	<pubDate>Fri, 17 Jun 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-06-17</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>6425</prism:startingPage>
		<prism:endingPage>6434</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Low-Cost Gas Sensors Produced by the Graphite Line-Patterning Technique Applied to Monitoring Banana Ripeness</dc:title>
	<dc:date>2011-06-17</dc:date>
	<dc:identifier>doi: 10.3390/s110606425</dc:identifier>
		<dc:creator>Alexandra Manzoli</dc:creator>
		<dc:creator>Clarice Steffens</dc:creator>
		<dc:creator>Rafaella T. Paschoalin</dc:creator>
		<dc:creator>Alessandra  A. Correa</dc:creator>
		<dc:creator>William F. Alves</dc:creator>
		<dc:creator>Fábio  L. Leite</dc:creator>
		<dc:creator>Paulo  S. P. Herrmann</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/6/6411/">
	<title>Sensors, Vol. 11, Pages 6411-6424: Nitrogen Concentration Estimation in Tomato Leaves by VIS-NIR Non-Destructive Spectroscopy</title>
	<link>http://www.mdpi.com/1424-8220/11/6/6411/</link>
	<description>Nitrogen concentration in plants is normally determined by expensive and time consuming chemical analyses. As an alternative, chlorophyll meter readings and N-NO3 concentration determination in petiole sap were proposed, but these assays are not always satisfactory. Spectral reflectance values of tomato leaves obtained by visible-near infrared spectrophotometry are reported to be a powerful tool for the diagnosis of plant nutritional status. The aim of the study was to evaluate the possibility and the accuracy of the estimation of tomato leaf nitrogen concentration performed through a rapid, portable and non-destructive system, in comparison with chemical standard analyses, chlorophyll meter readings and N-NO3 concentration in petiole sap. Mean reflectance leaf values were compared to each reference chemical value by partial least squares chemometric multivariate methods. The correlation between predicted values from spectral reflectance analysis and the observed chemical values showed in the independent test highly significant correlation coefficient (r = 0.94). The utilization of the proposed system, increasing efficiency, allows better knowledge of nutritional status of tomato plants, with more detailed and sharp information and on wider areas. More detailed information both in space and time is an essential tool to increase and stabilize crop quality levels and to optimize the nutrient use efficiency.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/6/6411/</guid>
	<pubDate>Thu, 16 Jun 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-06-16</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>6411</prism:startingPage>
		<prism:endingPage>6424</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Nitrogen Concentration Estimation in Tomato Leaves by VIS-NIR Non-Destructive Spectroscopy</dc:title>
	<dc:date>2011-06-16</dc:date>
	<dc:identifier>doi: 10.3390/s110606411</dc:identifier>
		<dc:creator>Valentina Ulissi</dc:creator>
		<dc:creator>Francesca Antonucci</dc:creator>
		<dc:creator>Paolo Benincasa</dc:creator>
		<dc:creator>Michela Farneselli</dc:creator>
		<dc:creator>Giacomo Tosti</dc:creator>
		<dc:creator>Marcello Guiducci</dc:creator>
		<dc:creator>Francesco Tei</dc:creator>
		<dc:creator>Corrado Costa</dc:creator>
		<dc:creator>Federico Pallottino</dc:creator>
		<dc:creator>Luigi Pari</dc:creator>
		<dc:creator>Paolo Menesatti</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/6/6145/">
	<title>Sensors, Vol. 11, Pages 6145-6164: The Multi-Chamber Electronic Nose—An Improved Olfaction Sensor for Mobile Robotics</title>
	<link>http://www.mdpi.com/1424-8220/11/6/6145/</link>
	<description>One of the major disadvantages of the use of Metal Oxide Semiconductor (MOS) technology as a transducer for electronic gas sensing devices (e-noses) is the long recovery period needed after each gas exposure. This severely restricts its usage in applications where the gas concentrations may change rapidly, as in mobile robotic olfaction, where allowing for sensor recovery forces the robot to move at a very low speed, almost incompatible with any practical robot operation. This paper describes the design of a new e-nose which overcomes, to a great extent, such a limitation. The proposed e-nose, called Multi-Chamber Electronic Nose (MCE-nose), comprises several identical sets of MOS sensors accommodated in separate chambers (four in our current prototype), which alternate between sensing and recovery states, providing, as a whole, a device capable of sensing changes in chemical concentrations faster. The utility and performance of the MCE-nose in mobile robotic olfaction is shown through several experiments involving rapid sensing of gas concentration and mobile robot gas mapping.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/6/6145/</guid>
	<pubDate>Tue, 07 Jun 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-06-07</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>6145</prism:startingPage>
		<prism:endingPage>6164</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>The Multi-Chamber Electronic Nose—An Improved Olfaction Sensor for Mobile Robotics</dc:title>
	<dc:date>2011-06-07</dc:date>
	<dc:identifier>doi: 10.3390/s110606145</dc:identifier>
		<dc:creator>Javier Gonzalez-Jimenez</dc:creator>
		<dc:creator>Javier G. Monroy</dc:creator>
		<dc:creator>Jose Luis Blanco</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/6/6109/">
	<title>Sensors, Vol. 11, Pages 6109-6124: Optimization of NIR Spectral Data Management for Quality Control of Grape Bunches during On-Vine Ripening</title>
	<link>http://www.mdpi.com/1424-8220/11/6/6109/</link>
	<description>NIR spectroscopy was used as a non-destructive technique for the assessment of chemical changes in the main internal quality properties of wine grapes (Vitis vinifera L.) during on-vine ripening and at harvest. A total of 363 samples from 25 white and red grape varieties were used to construct quality-prediction models based on reference data and on NIR spectral data obtained using a commercially-available diode-array spectrophotometer (380–1,700 nm). The feasibility of testing bunches of intact grapes was investigated and compared with the more traditional must-based method. Two regression approaches (MPLS and LOCAL algorithms) were tested for the quantification of changes in soluble solid content (SSC), reducing sugar content, pH-value, titratable acidity, tartaric acid, malic acid and potassium content. Cross-validation results indicated that NIRS technology provided excellent precision for sugar-related parameters (r2 = 0.94 for SSC and reducing sugar content) and good precision for acidity-related parameters (r2 ranging between 0.73 and 0.87) for the bunch-analysis mode assayed using MPLS regression. At validation level, comparison of LOCAL and MPLS algorithms showed that the non-linear strategy improved the predictive capacity of the models for all study parameters, with particularly good results for acidity-related parameters and potassium content.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/6/6109/</guid>
	<pubDate>Tue, 07 Jun 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-06-07</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>6109</prism:startingPage>
		<prism:endingPage>6124</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Optimization of NIR Spectral Data Management for Quality Control of Grape Bunches during On-Vine Ripening</dc:title>
	<dc:date>2011-06-07</dc:date>
	<dc:identifier>doi: 10.3390/s110606109</dc:identifier>
		<dc:creator>Virginia González-Caballero</dc:creator>
		<dc:creator>Dolores Pérez-Marín</dc:creator>
		<dc:creator>María-Isabel López</dc:creator>
		<dc:creator>María-Teresa Sánchez</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/6/5873/">
	<title>Sensors, Vol. 11, Pages 5873-5885: Preparation of a Porous Composite Film for the Fabrication of a Hydrogen Peroxide Sensor</title>
	<link>http://www.mdpi.com/1424-8220/11/6/5873/</link>
	<description>A series of dopant-type polyaniline-polyacrylic acid composite (PAn-PAA) films with porous structures were prepared and developed for an enzyme-free hydrogen peroxide (H2O2) sensor. The composite films were highly electroactive in a neutral environment as compared to polyaniline (PAn). In addition, the carboxyl group of the PAA was found to react with H2O2 to form peroxy acid groups, and the peroxy acid could further oxidize the imine structure of PAn to form N-oxides. The N-oxides reverted to their original form via electrochemical reduction and increased the reduction current. Based on this result, PAn-PAA was used to modify a gold electrode (PAn-PAA/Au) as a working electrode for the non-enzymatic detection of H2O2. The characteristics of the proposed sensors could be tuned by the PAA/PAn molar ratio. Blending PAA with PAn enhanced the surface area, electrocatalytic activity, and conductivity of these sensors. Under optimal conditions, the linear concentration range of the H2O2 sensor was 0.04 to 12 mM with a sensitivity of 417.5 μA/mM-cm2. This enzyme-free H2O2 sensor also exhibited a rapid response time, excellent stability, and high selectivity.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/6/5873/</guid>
	<pubDate>Tue, 31 May 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-05-31</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>5873</prism:startingPage>
		<prism:endingPage>5885</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Preparation of a Porous Composite Film for the Fabrication of a Hydrogen Peroxide Sensor</dc:title>
	<dc:date>2011-05-31</dc:date>
	<dc:identifier>doi: 10.3390/s110605873</dc:identifier>
		<dc:creator>Mu-Yi Hua</dc:creator>
		<dc:creator>Chun-Jen Chen</dc:creator>
		<dc:creator>Hsiao-Chien Chen</dc:creator>
		<dc:creator>Rung-Ywan Tsai</dc:creator>
		<dc:creator>Wen Cheng</dc:creator>
		<dc:creator>Chun-Lin Cheng</dc:creator>
		<dc:creator>Yin-Chih Liu</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/6/5740/">
	<title>Sensors, Vol. 11, Pages 5740-5753: Effects of Al(III) and Nano-Al13 Species on Malate Dehydrogenase Activity</title>
	<link>http://www.mdpi.com/1424-8220/11/6/5740/</link>
	<description>The effects of different aluminum species on malate dehydrogenase (MDH) activity were investigated by monitoring amperometric i-t curves for the oxidation of NADH at low overpotential using a functionalized multi-wall nanotube (MWNT) modified glass carbon electrode (GCE). The results showed that Al(III) and Al13 can activate the enzymatic activity of MDH, and the activation reaches maximum levels as the Al(III) and Al13 concentration increase. Our study also found that the effects of Al(III) and Al13 on the activity of MDH depended on the pH value and aluminum speciation. Electrochemical and circular dichroism spectra methods were applied to study the effects of nano-sized aluminum compounds on biomolecules.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/6/5740/</guid>
	<pubDate>Fri, 27 May 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-05-27</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>5740</prism:startingPage>
		<prism:endingPage>5753</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Effects of Al(III) and Nano-Al13 Species on Malate Dehydrogenase Activity</dc:title>
	<dc:date>2011-05-27</dc:date>
	<dc:identifier>doi: 10.3390/s110605740</dc:identifier>
		<dc:creator>Xiaodi Yang</dc:creator>
		<dc:creator>Ling Cai</dc:creator>
		<dc:creator>Yu Peng</dc:creator>
		<dc:creator>Huihui Li</dc:creator>
		<dc:creator>Rong Fu Chen</dc:creator>
		<dc:creator>Ren Fang Shen</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/6/5529/">
	<title>Sensors, Vol. 11, Pages 5529-5542: Odor Removal Characteristics of a Laminated Film-Electrode Packed-Bed Nonthermal Plasma Reactor</title>
	<link>http://www.mdpi.com/1424-8220/11/6/5529/</link>
	<description>Odor control has gained importance for ensuring a comfortable living environment. In this paper, the authors report the experimental results of a study on the detailed characteristics of a laminated film-electrode and a laminated film-electrode packed-bed nonthermal plasma reactor, which are types of dielectric barrier discharge (DBD) reactor used for odor control. These plasma reactors can be potentially used for the decomposition of volatile organic compounds (VOCs) and reduction of NOx. The reactor is driven by a low-cost 60-Hz neon transformer. Removal efficiencies under various experimental conditions are studied. The complete decomposition of the main odor component, namely, NH3, is achieved in a dry environment. The retention times are investigated for the complete removal of NH3 in the case of the film-electrode plasma reactor and the film-electrode packed-bed plasma reactor. The removal efficiency of the former reactor is lower than that of the latter reactor. Mixing another odor component such as CH3CHO in the gas stream has no significant effect on NH3 removal efficiency.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/6/5529/</guid>
	<pubDate>Wed, 25 May 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-05-25</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>6</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>5529</prism:startingPage>
		<prism:endingPage>5542</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Odor Removal Characteristics of a Laminated Film-Electrode Packed-Bed Nonthermal Plasma Reactor</dc:title>
	<dc:date>2011-05-25</dc:date>
	<dc:identifier>doi: 10.3390/s110605529</dc:identifier>
		<dc:creator>Takuya Kuwahara</dc:creator>
		<dc:creator>Masaaki Okubo</dc:creator>
		<dc:creator>Tomoyuki Kuroki</dc:creator>
		<dc:creator>Hideya Kametaka</dc:creator>
		<dc:creator>Toshiaki Yamamoto</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/5/5469/">
	<title>Sensors, Vol. 11, Pages 5469-5488: Cognitive Facilitation Following Intentional Odor Exposure</title>
	<link>http://www.mdpi.com/1424-8220/11/5/5469/</link>
	<description>This paper reviews evidence that, in addition to incidental olfactory pollutants, intentional odor delivery can impact cognitive operations both positively and negatively. Evidence for cognitive facilitation/interference is reviewed alongside four potential explanations for odor-induced effects. It is concluded that the pharmacological properties of odors can induce changes in cognition. However, these effects can be accentuated/attenuated by the shift in mood following odor exposure, expectancy of cognitive effects, and cues to behavior via the contextual association with the odor. It is proposed that greater consideration is required in the intentional utilization of odors within both industrial and private locations, since differential effects are observed for odors with positive hedonic qualities.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/5/5469/</guid>
	<pubDate>Thu, 19 May 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-05-19</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>5469</prism:startingPage>
		<prism:endingPage>5488</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Cognitive Facilitation Following Intentional Odor Exposure</dc:title>
	<dc:date>2011-05-19</dc:date>
	<dc:identifier>doi: 10.3390/s110505469</dc:identifier>
		<dc:creator>Andrew J. Johnson</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/5/5290/">
	<title>Sensors, Vol. 11, Pages 5290-5322: Odour Detection Methods: Olfactometry and Chemical Sensors</title>
	<link>http://www.mdpi.com/1424-8220/11/5/5290/</link>
	<description>The complexity of the odours issue arises from the sensory nature of smell. From the evolutionary point of view olfaction is one of the oldest senses, allowing for seeking food, recognizing danger or communication: human olfaction is a protective sense as it allows the detection of potential illnesses or infections by taking into account the odour pleasantness/unpleasantness. Odours are mixtures of light and small molecules that, coming in contact with various human sensory systems, also at very low concentrations in the inhaled air, are able to stimulate an anatomical response: the experienced perception is the odour. Odour assessment is a key point in some industrial production processes (i.e., food, beverages, etc.) and it is acquiring steady importance in unusual technological fields (i.e., indoor air quality); this issue mainly concerns the environmental impact of various industrial activities (i.e., tanneries, refineries, slaughterhouses, distilleries, civil and industrial wastewater treatment plants, landfills and composting plants) as sources of olfactory nuisances, the top air pollution complaint. Although the human olfactory system is still regarded as the most important and effective “analytical instrument” for odour evaluation, the demand for more objective analytical methods, along with the discovery of materials with chemo-electronic properties, has boosted the development of sensor-based machine olfaction potentially imitating the biological system. This review examines the state of the art of both human and instrumental sensing currently used for the detection of odours. The olfactometric techniques employing a panel of trained experts are discussed and the strong and weak points of odour assessment through human detection are highlighted. The main features and the working principles of modern electronic noses (E-Noses) are then described, focusing on their better performances for environmental analysis. Odour emission monitoring carried out through both the techniques is finally reviewed in order to show the complementary responses of human and instrumental sensing.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/5/5290/</guid>
	<pubDate>Mon, 16 May 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-05-16</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Review</prism:section>
	<prism:startingPage>5290</prism:startingPage>
		<prism:endingPage>5322</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Odour Detection Methods: Olfactometry and Chemical Sensors</dc:title>
	<dc:date>2011-05-16</dc:date>
	<dc:identifier>doi: 10.3390/s110505290</dc:identifier>
		<dc:creator>Magda Brattoli</dc:creator>
		<dc:creator>Gianluigi De Gennaro</dc:creator>
		<dc:creator>Valentina De Pinto</dc:creator>
		<dc:creator>Annamaria Demarinis Loiotile</dc:creator>
		<dc:creator>Sara Lovascio</dc:creator>
		<dc:creator>Michele Penza</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/5/5270/">
	<title>Sensors, Vol. 11, Pages 5270-5289: FT-IR-cPAS—New Photoacoustic Measurement Technique for Analysis of Hot Gases: A Case Study on VOCs</title>
	<link>http://www.mdpi.com/1424-8220/11/5/5270/</link>
	<description>This article describes a new photoacoustic FT-IR system capable of operating at elevated temperatures. The key hardware component is an optical-readout cantilever microphone that can work up to 200 °C. All parts in contact with the sample gas were put into a heated oven, incl. the photoacoustic cell. The sensitivity of the built photoacoustic system was tested by measuring 18 different VOCs. At 100 ppm gas concentration, the univariate signal to noise ratios (1σ, measurement time 25.5 min, at highest peak, optical resolution 8 cm−1) of the spectra varied from minimally 19 for o-xylene up to 329 for butyl acetate. The sensitivity can be improved by multivariate analyses over broad wavelength ranges, which effectively co-adds the univariate sensitivities achievable at individual wavelengths. The multivariate limit of detection (3σ, 8.5 min, full useful wavelength range), i.e., the best possible inverse analytical sensitivity achievable at optimum calibration, was calculated using the SBC method and varied from 2.60 ppm for dichloromethane to 0.33 ppm for butyl acetate. Depending on the shape of the spectra, which often only contain a few sharp peaks, the multivariate analysis improved the analytical sensitivity by 2.2 to 9.2 times compared to the univariate case. Selectivity and multi component ability were tested by a SBC calibration including 5 VOCs and water. The average cross selectivities turned out to be less than 2% and the resulting inverse analytical sensitivities of the 5 interfering VOCs was increased by maximum factor of 2.2 compared to the single component sensitivities. Water subtraction using SBC gave the true analyte concentration with a variation coefficient of 3%, although the sample spectra (methyl ethyl ketone, 200 ppm) contained water from 1,400 to 100k ppm and for subtraction only one water spectra (10k ppm) was used. The developed device shows significant improvement to the current state-of-the-art measurement methods used in industrial VOC measurements.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/5/5270/</guid>
	<pubDate>Mon, 16 May 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-05-16</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>5270</prism:startingPage>
		<prism:endingPage>5289</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>FT-IR-cPAS—New Photoacoustic Measurement Technique for Analysis of Hot Gases: A Case Study on VOCs</dc:title>
	<dc:date>2011-05-16</dc:date>
	<dc:identifier>doi: 10.3390/s110505270</dc:identifier>
		<dc:creator>Christian Bernd Hirschmann</dc:creator>
		<dc:creator>Niina Susanna Koivikko</dc:creator>
		<dc:creator>Jussi Raittila</dc:creator>
		<dc:creator>Jussi Tenhunen</dc:creator>
		<dc:creator>Satu Ojala</dc:creator>
		<dc:creator>Katariina Rahkamaa-Tolonen</dc:creator>
		<dc:creator>Ralf Marbach</dc:creator>
		<dc:creator>Sarah Hirschmann</dc:creator>
		<dc:creator>Riitta Liisa Keiski</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/5/5047/">
	<title>Sensors, Vol. 11, Pages 5047-5057: 
Performance of a CO2 Impedimetric Sensor Prototype for Air Quality Monitoring
 
Performance of a CO2 Impedimetric Sensor Prototype for Air Quality Monitoring
</title>
	<link>http://www.mdpi.com/1424-8220/11/5/5047/</link>
	<description>Carbon dioxide detection is a relevant issue in many fields, and this work focuses on the use of a BaTiO3-CuO sputtered thin film layer in a gas sensor prototype for air quality measurements. For this, a double side sensor was fabricated, with a Pt heater on one side and the sensing layer over the electrodes on the other side. The uniformity of the temperature on the sensing layer was tested and further tests to check its sensing performance were carried out. Humidity influence in the detection was found to be almost negligible within the usual range in air quality measurements and repeatability tests show satisfactory results for air quality control purposes.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/5/5047/</guid>
	<pubDate>Thu, 05 May 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-05-05</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>5047</prism:startingPage>
		<prism:endingPage>5057</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>
Performance of a CO2 Impedimetric Sensor Prototype for Air Quality Monitoring
 
Performance of a CO2 Impedimetric Sensor Prototype for Air Quality Monitoring
</dc:title>
	<dc:date>2011-05-05</dc:date>
	<dc:identifier>doi: 10.3390/s110505047</dc:identifier>
		<dc:creator>Gemma García Mandayo</dc:creator>
		<dc:creator>Jaime Herrán</dc:creator>
		<dc:creator>Irene Castro-Hurtado</dc:creator>
		<dc:creator>Enrique Castaño</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/5/4830/">
	<title>Sensors, Vol. 11, Pages 4830-4839: Rapid Assessment of Mineral Concentration in Meadow Grasses by Near Infrared Reflectance Spectroscopy</title>
	<link>http://www.mdpi.com/1424-8220/11/5/4830/</link>
	<description>A near infrared reflectance spectroscopy (NIRS) method for rapid determination of nitrogen, phosphorous and potassium in diverse meadow grasses was developed with a view towards utilizing this material for biogas production and organic fertilizer. NIRS spectra between 12,000 cm−1 and 4,000 cm−1 were used. When validated on samples from different years to those used for the calibration set, the NIRS prediction of nitrogen was considered moderately useful with R2 = 0.77, ratio of standard error of prediction to reference data range (RER) of 9.32 and ratio of standard error of prediction to standard deviation of reference data (RPD) of 2.33. Prediction of potassium was less accurate, with R2 = 0.77, RER of 6.56 and RPD of 1.45, whilst prediction of phosphorous was not considered accurate enough to be of any practical use. This work is of interest from the point of view of both the removal of excess nutrients from formerly intensively farmed areas and also for assessing the plant biomass suitability for conversion into carbon neutral energy through biogas production.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/5/4830/</guid>
	<pubDate>Tue, 03 May 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-05-03</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>4830</prism:startingPage>
		<prism:endingPage>4839</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Rapid Assessment of Mineral Concentration in Meadow Grasses by Near Infrared Reflectance Spectroscopy</dc:title>
	<dc:date>2011-05-03</dc:date>
	<dc:identifier>doi: 10.3390/s110504830</dc:identifier>
		<dc:creator>Alastair Ward</dc:creator>
		<dc:creator>Anne Lisbeth Nielsen</dc:creator>
		<dc:creator>Henrik Møller</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/5/4674/">
	<title>Sensors, Vol. 11, Pages 4674-4687: A Novel Ionic Polymer Metal ZnO Composite (IPMZC)</title>
	<link>http://www.mdpi.com/1424-8220/11/5/4674/</link>
	<description>The presented research introduces a new Ionic Polymer-Metal-ZnO Composite (IPMZC) demonstrating photoluminescence (PL)-quenching on mechanical bending or application of an electric field. The newly fabricated IPMZC integrates the optical properties of ZnO and the electroactive nature of Ionic Polymer Metal Composites (IPMC) to enable a non-contact read-out of IPMC response. The electro-mechano-optical response of the IPMZC was measured by observing the PL spectra under mechanical bending and electrical regimes. The working range was measured to be 375–475 nm. It was noted that the PL-quenching increased proportionally with the increase in curvature and applied field at 384 and 468 nm. The maximum quenching of 53.4% was achieved with the membrane curvature of 78.74/m and 3.01% when electric field (12.5 × 103 V/m) is applied. Coating IPMC with crystalline ZnO was observed to improve IPMC transduction.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/5/4674/</guid>
	<pubDate>Thu, 28 Apr 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-04-28</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>4674</prism:startingPage>
		<prism:endingPage>4687</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>A Novel Ionic Polymer Metal ZnO Composite (IPMZC)</dc:title>
	<dc:date>2011-04-28</dc:date>
	<dc:identifier>doi: 10.3390/s110504674</dc:identifier>
		<dc:creator>Sang-Mun Kim</dc:creator>
		<dc:creator>Rashi Tiwari</dc:creator>
		<dc:creator>Kwang J. Kim</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/5/4648/">
	<title>Sensors, Vol. 11, Pages 4648-4655: Investigation of a Photoelectrochemical Passivated ZnO-Based Glucose Biosensor</title>
	<link>http://www.mdpi.com/1424-8220/11/5/4648/</link>
	<description>A vapor cooling condensation system was used to deposit high quality intrinsic ZnO thin films and intrinsic ZnO nanorods as the sensing membrane of extended-gate field-effect-transistor (EGFET) glucose biosensors. The sensing sensitivity of the resulting glucose biosensors operated in the linear range was 13.4 μA mM−1 cm−2. To improve the sensing sensitivity of the ZnO-based glucose biosensors, the photoelectrochemical method was utilized to passivate the sidewall surfaces of the ZnO nanorods. The sensing sensitivity of the ZnO-based glucose biosensors with passivated ZnO nanorods was significantly improved to 20.33 μA mM−1 cm−2 under the same measurement conditions. The experimental results verified that the sensing sensitivity improvement was the result of the mitigation of the Fermi level pinning effect caused by the dangling bonds and the surface states induced on the sidewall surface of the ZnO nanorods.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/5/4648/</guid>
	<pubDate>Thu, 28 Apr 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-04-28</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>4648</prism:startingPage>
		<prism:endingPage>4655</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Investigation of a Photoelectrochemical Passivated ZnO-Based Glucose Biosensor</dc:title>
	<dc:date>2011-04-28</dc:date>
	<dc:identifier>doi: 10.3390/s110504648</dc:identifier>
		<dc:creator>Ching-Ting Lee</dc:creator>
		<dc:creator>Ying-Shuo Chiu</dc:creator>
		<dc:creator>Shu-Ching Ho</dc:creator>
		<dc:creator>Yao-Jung Lee</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/5/4609/">
	<title>Sensors, Vol. 11, Pages 4609-4621: An Electronic-Nose Sensor Node Based on a Polymer-Coated Surface Acoustic Wave Array for Wireless Sensor Network Applications</title>
	<link>http://www.mdpi.com/1424-8220/11/5/4609/</link>
	<description>This study developed an electronic-nose sensor node based on a polymer-coated surface acoustic wave (SAW) sensor array. The sensor node comprised an SAW sensor array, a frequency readout circuit, and an Octopus II wireless module. The sensor array was fabricated on a large K2 128° YX LiNbO3 sensing substrate. On the surface of this substrate, an interdigital transducer (IDT) was produced with a Cr/Au film as its metallic structure. A mixed-mode frequency readout application specific integrated circuit (ASIC) was fabricated using a TSMC 0.18 μm process. The ASIC output was connected to a wireless module to transmit sensor data to a base station for data storage and analysis. This sensor node is applicable for wireless sensor network (WSN) applications.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/5/4609/</guid>
	<pubDate>Thu, 28 Apr 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-04-28</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>4609</prism:startingPage>
		<prism:endingPage>4621</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>An Electronic-Nose Sensor Node Based on a Polymer-Coated Surface Acoustic Wave Array for Wireless Sensor Network Applications</dc:title>
	<dc:date>2011-04-28</dc:date>
	<dc:identifier>doi: 10.3390/s110504609</dc:identifier>
		<dc:creator>Kea-Tiong Tang</dc:creator>
		<dc:creator>Cheng-Han Li</dc:creator>
		<dc:creator>Shih-Wen Chiu</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>
	<item rdf:about="http://www.mdpi.com/1424-8220/11/5/4598/">
	<title>Sensors, Vol. 11, Pages 4598-4608: Fluorescent Sensing of Chlorophenols in Water Using an Azo Dye Modified β-Cyclodextrin Polymer</title>
	<link>http://www.mdpi.com/1424-8220/11/5/4598/</link>
	<description>A water soluble azo dye modified β-cyclodextrin polymer 4 was synthesized and used as a chemosensor for the detection of chlorinated phenols, model chlorinated by-products (CBPs) of water treatment for drinking purposes. The characterization of the intermediates and the azo dye modified β-CD polymer was done by UV/Vis Spectrophotometry, FT-IR and 1H-NMR spectroscopies. The chlorophenols were capable of quenching the fluorescence of the polymer. The polymer showed greater sensitivity towards 2,4-dichlorophenol, with a sensitivity factor of 0.35 compared to 0.05 and 0.12 for phenol and 4-chlorophenol, respectively. The stability constants (Ks) of the pollutants were also determined by the Benesi-Hildebrand method to be 2.104 × 103 M−1 for 2,4-dichlorophenol and 1.120 × 102 M−1 for 4-chlorophenol.</description>
	
	<guid>http://www.mdpi.com/1424-8220/11/5/4598/</guid>
	<pubDate>Wed, 27 Apr 2011 00:00:00 CEST</pubDate>
	
	<prism:publicationName>Sensors</prism:publicationName>
	<prism:publicationDate>2011-04-27</prism:publicationDate>
	<prism:volume>11</prism:volume>
	<prism:number>5</prism:number>
	<prism:section>Article</prism:section>
	<prism:startingPage>4598</prism:startingPage>
		<prism:endingPage>4608</prism:endingPage>
		<prism:issn>1424-8220</prism:issn>
	
	<dc:title>Fluorescent Sensing of Chlorophenols in Water Using an Azo Dye Modified β-Cyclodextrin Polymer</dc:title>
	<dc:date>2011-04-27</dc:date>
	<dc:identifier>doi: 10.3390/s110504598</dc:identifier>
		<dc:creator>Phendukani Ncube</dc:creator>
		<dc:creator>Rui W. Krause</dc:creator>
		<dc:creator>Bhekie B. Mamba</dc:creator>
	
	<cc:license rdf:resource="http://creativecommons.org/licenses/by/3.0/" />
</item>


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