Search Results (110)

This study investigated the effect of in situ polymerization on the compressive strength of demolition-derived Scots pine, European beech, and black alder wood. The treatment applied was based on previously confirmed in situ polymerization systems in wood, which are known to lead to polymer formation and composite-like structures. In this study, we assumed similar behavior and focused on a mechanical evaluation of the modified wood. Three different polymer systems were applied to evaluate differences in performance. After modification, the compressive strength levels increased by 60% in beech, 119% in alder, and 150% in pine, with corresponding increases in density and weight percent gain (WPG). The highest relative improvement was observed in the least dense species, pine. The findings suggest that polymer treatment can significantly enhance the mechanical properties, likely due to the incorporation of polymer into the wood matrix; however, this inference is based on indirect physical evidence. Full article

The valuation of the benefits to humans of ecosystem services (ESs) provided by nature has become increasingly important. A current challenge is the measurement of the range of benefits which are not traded in the marketplace and are generally considered intangible, with further challenges to even classify them formally, e.g., as cultural ecosystem services (CESs). Previous studies have emphasized a related challenge: the strong need for engagement of not just experts but ’ordinary people’. Approaches using participatory approaches and less formal communication pathways to draw out local CES values have been reported. However, critical reflections of those studies reported significant differences in understanding between ’outsider researchers’ and ’locals’, calling validity deeply into question. Even deliberative approaches backfired by significantly modifying local social constructs during elicitation. In this study, we demonstrate a fundamentally different kind of approach, developed from the bottom–up sustainability indicator development process called WeValue InSitu. It focuses not on improving deeper top–down ‘engagement’ of a specific topic, but instead on improving local articulation of existing envelopes of in situ human shared values, naturally integrated. The WeValue InSitu output is a framework of separate but interlinked concise Statements of local shared values. Some of these Statements may refer to values concerning ecosystems, but situated amongst others. Here, we analyze the outputs from 23 convenience groups in three sites in Nigeria and investigate the shared values found empirically against existing economics-based MEA classifications. The findings include hybrid values which span existing CES sub-categories and even across into market-based categories. This opens a discussion as to whether future ES valuation frameworks might evolve more usefully with foundations built on empirically derived typologies of human values, rather than bolt-on modifications to financially based economics concepts. It also raises questions about the validity of current valuations made which cannot capture empirically found human values. Full article

Nonribosomal peptide synthetases (NRPS) are essential for the biosynthesis of therapeutically valuable molecules, including antibiotics, immunosuppressants, and anticancer agents. The assembly-line mechanism of NRPS offers significant potential for engineering novel natural products through reprogramming. However, the challenging purification of NRPS proteins has impeded the investigation of their assembly and catalytic mechanisms. In this study, we employed homologous recombination to insert a purification tag at the C-terminus of the NRPS gene within the chromosome. This genetic modification enabled efficient purification of NRPS proteins from the tagged mutant strain using a one-step affinity chromatography approach. Additionally, we discovered that MbtH-like proteins (MLPs) form stable complexes with all pyoverdine (PVD) NRPS subunits, allowing for the purification of the entire NRPS assembly line via tagged MLP. Negative stain electron microscopy analysis revealed that the purified PVD NRPS proteins exist as dynamically linear monomers. Our in-situ tag-based purification method enhances NRPS research in both biochemical and structural biology, providing a robust platform for further investigations into NRPS mechanisms and applications. Full article

V/Fe multilayers were prepared on naturally oxidized Si(100) substrates at room temperature (RT) by UHV magnetron sputtering. Mixing effects at the Fe–V interfaces were investigated in-situ, directly after deposition, by means of X-ray photoelectron spectroscopy (XPS). The results of systematic in-situ XPS studies of the integral intensity of the Fe-2p peak, as a function of the nominal thickness of the Fe sublayer deposited on vanadium, allowed us to estimate the thickness of the pure iron layer that forms the mixed layer at about 0.4 nm. Assuming the same thickness of the vanadium layer that forms the mixed layer, the estimated thickness of the mixed layer near the Fe–V interface was about 0.8 nm. In the analysis of magnetic hysteresis loops, in addition to the bilinear (J₁) and biquadratic (J₂) coupling constant, the contribution of the cubic exchange constant (J₃) was taken into account, which also contributed significantly to the total energy. Higher order interactions (J₂ and J₃) are particularly important for V spacer thicknesses greater than 7 atomic monolayers. Hydrogen absorption in V/Fe multilayers at RT and a pressure of about 1 bar causes an increase in the biquadratic coupling constant J₂, while the values of J₁ and J₃ are reduced. A comparison of the obtained experimental results and available theoretical models leads to the conclusion that the mechanism of “fluctuating thickness of the non-magnetic spacer” could be responsible for the biquadratic exchange coupling. On the other hand, the “loose spins” model can explain the cubic coupling in the V/Fe multilayers. The modification of the interlayer exchange coupling using hydrogen is fully reversible. Full article

There is much promise for creating metal organic framework (MOF) films on metal substrates in fields including sensing and electrical conduction. For these applications, direct production of MOF films with strong bonding on metal substrates is extremely desirable. In this study, a simple one-step method without the need for additives or pre-modification is used to directly create zeolitic imidazolate framework-8 (ZIF-8) films with strong bonding on zinc substrate. The formation mechanisms of ZIF-8 film are analyzed. The strong bonding ZIF-8 film can be attributed to an in-situ grown ZnO interlayer between the ZIF-8 and substrate. The growth process shows the formation time of zinc oxide on the substrate, which is subsequently covered by ZIF-8 crystals. The ZnO interlayer results from a combination of decomposition products of the solvent and the zinc ions. Furthermore, the ZnO interlayer serves as a sacrificial precursor for the in-situ nucleation and continuous growth of ZIF-8 film. It serves as an anchoring site between ZIF-8 film and substrate, resulting in strong adhesion. This paper describes a simple and straightforward production process that is expected to provide a theoretical basis for the laboratory preparation of ZIF films. Full article

LiFePO₄ is a cathode material for lithium (Li)-ion batteries known for its excellent performance. However, compared with layered oxides and other ternary Li-ion battery materials, LiFePO₄ cathode material exhibits low electronic conductivity due to its structural limitations. This limitation significantly impacts the charge/discharge rates and practical applications of LiFePO₄. This paper reviews recent advancements in strategies aimed at enhancing the electronic conductivity of LiFePO₄. Efficient strategies with a sound theoretical basis, such as in-situ carbon coating, the establishment of multi-dimensional conductive networks, and ion doping, are discussed. Theoretical frameworks underlying the conductivity enhancement post-modification are summarized and analyzed. Finally, future development trends and research directions in carbon coating and doping are anticipated. Full article

The application of superamphiphobic coatings improves the surface’s ability to repel fluids, thereby greatly enhancing its various functions, including anti-fouling, anti-corrosion, anti-icing, anti-bacterial, and self-cleaning properties. This maximizes the material’s potential for industrial applications. This work utilized the agglomeration phenomenon exhibited by nano-spherical titanium dioxide (TiO₂) particles to fabricate 1H,1H,2H,2H-perfluorodecyltriethoxysilane (PFDTES) modified TiO₂ (TiO₂@fluoroPOS) fillers with low surface energy. This was achieved through the in-situ formation of protective armor on the surface of the agglomerates using the sol-gel method and fluorination modification. Polyvinylidene fluoride-tetrafluoropropylene (PVDF-HFP) and TiO₂@fluoroPOS fillers were combined using a spraying technique to prepare P/TiO₂@fluoroPOS coatings with superamphiphobicity. Relying on the abundance of papillae, micropores, and other tiny spaces on the surface, the coating can capture a stable air film and reject a variety of liquids. When the coatings were immersed in solutions of 2 mol/L HCl, NaCl, and NaOH for a duration of 12 h, they retained their exceptional superamphiphobic properties. Owing to the combined influence of the armor structure and the organic binder, the coating exhibited good liquid repellency during water jetting and sandpaper abrasion tests. Furthermore, the coating has shown exceptional efficacy in terms of its ability to be anti-icing, anti-waxing, and self-cleaning. Full article

Fused Deposition Modeling (FDM) is an additive manufacturing technology that has emerged as a promising technique for fabricating 3D printed polymers. It has gained attention recently due to its ease of use, efficiency, low cost, and safety. However, 3D-printed FDM components lack sufficient strength compared to those made using conventional manufacturing methods. This low strength can be mainly attributed to high porosity and low sinterability of layers and then to the characteristics of the polymer used in the FDM process or the FDM process itself. Regarding polymer characteristics, there are two main types of reinforcing fibers: discontinuous (short) and continuous. Continuous-fiber reinforced composites are becoming popular in various industries due to their excellent mechanical properties. Since continuous reinforcing fibers have a more positive effect on increasing the strength of printed parts, this article focuses primarily on continuous long fibers. In addition to polymer characteristics, different mechanisms have been developed and introduced to address the issue of insufficient strength in 3D-printed FDM parts. This article comprehensively explains two main FDM mechanisms: in-situ fusion and ex-situ prepreg. It also provides relevant examples of these mechanisms using different reinforcing elements. Additionally, some other less frequently utilized mechanisms are discussed. Each mechanism has its own advantages and disadvantages, indicating that further development and modification are needed to increase the strength of 3D-printed FDM parts to be comparable to those produced using traditional methods. Full article

Chiral nematic materials have been attracting attention in fields of advanced functional applications due to their unique iridescent colors and tunable helical structure. A precisely decreased pitch is of importance for construction and applications of chiral nematic materials; however, it remains a huge challenge. Herein, cellulose nanocrystal (CNC) is selected as a constructed matrix for chiral nematic films, and ferric chloride (FeCl₃) is used as a modification agent. We investigate the effects of the ferric ion loads on the helical structure and optical characteristics of iridescent film. Subsequently, the influence of ferric ions on the assembly process of CNC liquid crystal and the regulation of the structure color of self-assembled monolayers are discussed. Therefore, the CNC/FeCl₃ chiral nematic films showed a blueshifted structural color from orange to blue, which highlights a simple route to achieve the regulation of decreased pitch. Further, we have applied this CNC/FeCl₃ chiral nematic film for benzene gas detection. The sensing performance shows that the CNC/FeCl₃ chiral nematic film reacts to benzene gas, which can be merged into the nematic layer of the CNC and trigger the iron ions chelated on the CNC, consequently arousing the redshift of the reflected wavelength and the effective colorimetric transition. This CNC/FeCl₃ chiral nematic film is anticipated to boost a new gas sensing mechanism for faster and more effective in-situ qualitative investigations. Full article

Argillaceous limestone (AL) is comprised of carbonate minerals and clay minerals and is widely distributed throughout the Earth’s crust. However, owing to its low surface area and poorly active sites, AL has been largely neglected. Herein, manganic manganous oxide (Mn₃O₄) was used to modify AL by an in-situ deposition strategy through manganese chloride and alkali stepwise treatment to improve the surface area of AL and enable its utilization as an efficient adsorbent for heavy metals removal. The surface area and cation exchange capacity (CEC) were enhanced from 3.49 to 24.5 m²/g and 5.87 to 31.5 cmoL(+)/kg with modification, respectively. The maximum adsorption capacities of lead (Pb²⁺), copper (Cu²⁺), and nickel (Ni²⁺) ions on Mn₃O₄-modified argillaceous limestone (Mn₃O₄–AL) in mono-metal systems were 148.73, 41.30, and 60.87 mg/g, respectively. In addition, the adsorption selectivity in multi-metal systems was Pb²⁺ > Cu²⁺ > Ni²⁺ in order. The adsorption process conforms to the pseudo-second-order model. In the multi-metal system, the adsorption reaches equilibrium at about 360 min. The adsorption mechanisms may involve ion exchange, precipitation, electrostatic interaction, and complexation by hydroxyl groups. These results demonstrate that Mn₃O₄ modification realized argillaceous limestone resourcization as an ideal adsorbent. Mn₃O₄-modified argillaceous limestone was promising for heavy metal-polluted water and soil treatment. Full article

In unsaturated glycerol polyesters, the C=C bond is present. It makes it possible to carry out post-polymerisation modification (PPM) reactions, such as aza-Michael addition. This reaction can conduct crosslinking under in-situ conditions for tissue engineering regeneration. Until now, no description of such use of aza-Michael addition has been described. This work aims to crosslink the synthesised poly(glycerol itaconate) (PGItc; P3), polyester from itaconic acid (Ac_Itc), and glycerol (G). The PGItc syntheses were performed in three ways: without a catalyst, in the presence of p-toluenesulfonic acid (PTSA), and in the presence of zinc acetate (Zn(OAc)₂). PGItc obtained with Zn(OAc)₂ (150 °C, 4 h, G:Ac_Itc = 2:1) was used to carry out the aza-Michael additions. Crosslinking reactions were conducted with each of the five aliphatic diamines: 1,2-ethylenediamine (1,2-EDA; A1), 1,4-butanediamine (1,4-BDA; A2), 1,6-hexanediamine (1,6-HDA; A3), 1,8-octanediamine (1,8-ODA; A4), and 1,10-decanediamine (1,10-DDA; A5). Four ratios of the proton amine group: C=C bond were investigated. The maximum temperature and crosslinking time were measured to select the best amine for the addition product’s application. FTIR, ¹H NMR, DSC, and TG analysis of the crosslinked products were also investigated. Full article

Accurate quantification of ecosystem water use efficiency (eWUE) over agroecosystems is crucial for managing water resources and assuring food security. Currently, the uncoupled Moderate Resolution Imaging Spectroradiometer (MODIS) product is the most widely applied dataset for simulating local, regional, and global eWUE across different plant functional types. However, it has been rarely investigated as to whether the coupled product can outperform the uncoupled product in eWUE estimations for specific C4 and C3 crop species. Here, the eWUE as well as gross primary production (GPP) and evapotranspiration (ET) from the uncoupled MODIS product and the coupled Penman–Monteith–Leuning version 2 (PMLv2) product were evaluated against the in-situ observations on eight-day and annual scales (containing 1902 eight-day and 61 annual samples) for C4 maize and C3 soybean at the five cropland sites from the FLUXNET2015 and AmeriFlux datasets. Our results show the following: (1) For GPP estimates, the PMLv2 product showed paramount improvements for C4 maize and slight improvements for C3 soybean, relative to the MODIS product. (2) For ET estimates, both products performed similarly for both crop species. (3) For eWUE estimates, the coupled PMLv2 product achieved higher-accuracy eWUE estimates than the uncoupled MODIS product at both eight-day and annual scales. Taking the result at an eight-day scale for example, compared to the MODIS product, the PMLv2 product could reduce the root mean square error (RMSE) from 2.14 g C Kg⁻¹ H₂O to 1.36 g C Kg⁻¹ H₂O and increase the coefficient of determination (R²) from 0.06 to 0.52 for C4 maize, as well as reduce the RMSE from 1.33 g C Kg⁻¹ H₂O to 0.89 g C Kg⁻¹ H₂O and increase the R² from 0.05 to 0.49 for C3 soybean. (4) Despite the outperformance of the PMLv2 product in eWUE estimations, both two products failed to differentiate C4 and C3 crop species in their model calibration and validation processes, leading to a certain degree of uncertainties in eWUE estimates. Our study not only provides an important reference for applying remote sensing products to derive reliable eWUE estimates over cropland but also indicates the future modification of the current remote sensing models for C4 and C3 crop species. Full article

Pre-treated silica with a plasma-deposited (PD) layer of polymerized precursors was tested concerning its compatibility with Natural Rubber (NR) and its influence on the processing of silica-silane compounds. The modification was performed in a tailor-made plasma reactor. The degree of deposition of the plasma-coated samples was analyzed by ThermoGravimetric Analysis (TGA). In addition, Diffuse Reflectance Infrared Fourier Transform spectroscopy (DRIFTs), X-ray Photoelectron Spectroscopy (XPS), and Transmission Electron Microscopy (TEM) were performed to identify the morphology of the deposited plasma polymer layer on the silica surface. PD silica samples were incorporated into a NR/silica model compound. NR compounds containing untreated silica and in-situ silane-modified silica were taken as references. The silane coupling agent used for the reference compounds was bis-(3-triethoxysilyl-propyl)disulfide (TESPD), and reference compounds with untreated silica having the full amount and 50% of silane were prepared. In addition, 50% of the silane was added to the PD silica-filled compounds in order to verify the hypothesis that additional silane coupling agents can react with silanol groups stemming from the breakdown of the silica clusters during mixing. The acetylene PD silica with 50% reduced silane-filled compounds presented comparable properties to the in-situ silane-modified reference compound containing 100% TESPD. This facilitates processing as lower amounts of volatile organic compounds, such as ethanol, are generated compared to the conventional silica-silane filler systems. Full article

The hydrophobic/hydrophilic character of some conductive polymer (CP) coatings can be switched in the function of the working conditions of these adaptive materials. We studied the influence of electrical stimuli and intrinsic physical characteristics (nature of the polymerizable core, dopants, the droplet dimension and physical properties, surface roughness, etc.) on the CP wettability. A simulation strategy was developed for determining the contact angle (CA) of a liquid droplet on a CP layer with roughness. The method was tested for new reported CP composites, but with new dopants. The results indicate that the influences on the material wettability are correlated, and in practice, modification of more than one parameter converges to a wanted behavior of the material. E.g., the CP porous film of poly(3-hexylthiophene) (P3HT) + [6,6]-phenyl-C61-butyricacid-methyl-ester (PCBM) changes its wettability at voltages of up to 26 V, but if doping ions are inserted and the roughness geometry is modified, the voltage decreases twice. Our multi-parametrical study points out that the polymer wettability type is driven by the voltage, but this effect is tuned differently by each internal parameter. The thin films’ effect and the dopants (in-situ and ex-situ) significantly decrease the actuation voltage. We also illustrated that the wettability type does not change for specific sets of parameters. Full article

Acrylonitrile butadiene styrene (ABS) is a thermoplastic polymer widely used in several everyday life applications; moreover, it is also one of the most employed plastics in contemporary artworks and design objects. In this study, the chemical and thermal properties of an ABS-based polymer and its photo-degradation process were investigated through a multi-analytical approach based on thermal, mass spectrometric and spectroscopic techniques. LEGO^® building blocks were selected for studying the ABS properties. First, the composition of unaged LEGO^® bricks was determined in terms of polymer composition and thermal stability; then, the bricks were subjected to UV–Vis photo-oxidative-accelerated ageing for evaluation of possible degradation processes. The modifications of the chemical and thermal properties were monitored in time by a multi-technique approach aimed at improving the current knowledge of ABS photodegradation, employing pyrolysis online with gas chromatography and evolved gas analysis, coupled with mass spectrometric detection (Py-GC-MS and EGA-MS), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and corroborated by external reflection FT-IR spectroscopy. The multimodal approach provided new evidence on the two-step degradation pathway proposed for ABS, defining molecular markers for polybutadiene oxidation and styrene-acrylonitrile depolymerization. Moreover, the results highlighted the feasibility of correlating accurate compositional and thermal data acquired by bulk techniques with external reflection FT-IR spectroscopy as a non-invasive portable tool to monitor the state of conservation of plastic museum objects in-situ. Full article