Editor’s Choice Articles

Harm reduction drug checking utilizing paper spray mass spectrometry (PS-MS) has been the focus of ongoing research since 2017 and has seen many refinements. The presented work is the result of this research and has led to the public-facing PS-MS use for on-site drug checking in Victoria, BC. Included are the improved methods and approaches required to develop and implement PS-MS as an on-site drug checking technology. Critical details regarding appropriate direct mass spectrometry tune and calibration suites required to avoid isobaric interferences, calibration details, quality control strategies, detailed MS scan approaches to implement rapid drug tests, as well as future work considerations are presented. The PS-MS method presented currently directly quantifies 107 targeted drugs in a two-minute measurement, and can be easily adapted to include additional new targets that appear in the unregulated drug supply that are detected by either low or high resolution PS-MS. The presented methodologies provide a framework to assist those interested in implementing PS-MS to reduce harms from the toxic drug supply, but will have value for those developing rapid, quantitative drug testing for other applications. Full article

Ferulic acid (FA) is well known for its antioxidant properties and neuroprotective effects. To enhance these biological activities, we designed a novel series of FA derivatives by introducing a phenyl group at the α-position of the carboxyl moiety. Further structural modifications were achieved by incorporating hydroxy or alkoxy substituents at various positions on the two aromatic rings. A series of these derivatives were synthesized and evaluated for their antioxidant capacity using the DPPH radical scavenging assay, as well as their cytoprotective effects against oxidative stress in Neuro-2a cells. Among the synthesized compounds, one derivative exhibited significantly enhanced activity in both assays. Mechanistic studies indicated that this heightened efficacy is attributable to a unique reaction pathway involving dual antioxidant mechanisms. Full article

Lithium-ion batteries (LIBs) are vital for modern energy storage applications. Lithium iron phosphate (LFP) is a promising cathode material due to its safety, low cost, and environmental friendliness compared to the widely used nickel manganese cobalt oxide (NMC), which contains hazardous nickel and cobalt compounds. However, challenges remain in enhancing the performance of LFP cathodes due to their low electronic and ionic conductivity. To improve both the safety and sustainability of the battery, this work presents a water-based LFP cathode utilizing the bio-based binder carboxymethyl cellulose (CMC), eliminating the need for polyvinylidene fluoride (PVDF) and the toxic solvent N-methyl-2-pyrrolidone (NMP). This study investigates the impact of different dispersing methods—dissolver mixing and wet jet milling—on slurry properties, electrode morphology, and battery performance. Slurries were characterized by rheology, particle size distribution, and sedimentation behavior, while coated and calendered electrodes were examined via thickness measurements and scanning electron microscopy (SEM). Electrochemical performance of the electrodes was evaluated by means of C-Rate testing. The results reveal that dispersing methods significantly influence slurry characteristics but marginally affect electrochemical performance. Compared to dissolver mixing, wet jet milling reduced the median particle size by 39% (ΔD50 = 3.1 µm) and lowered viscosity by 96% at 1 s⁻¹, 80% at 105 s⁻¹, and 64% at 1000 s⁻¹. In contrast, the electrochemical performance of the resulting electrodes differed only slightly, with discharge capacity varying by approximately 12.8% at 1.0 C (Δcapacity = 10.7 mAh g⁻¹). This research highlights the importance of optimizing not only material selection but also processing techniques to advance safer and more sustainable energy storage solutions. Full article

In today’s chemistry, greener and more energy-efficient ways of making new materials are becoming increasingly important. In this work, two types of (3-aminopropyl) triethoxysilane-grafted silica were synthesized using a one-pot method with two different porogens: Pluronic P123 and cetyltrimethylammonium bromide, and then modified with silver nanoparticles. Both syntheses produced amorphous silica with crystalline silver. EDX and EDX elemental mapping confirmed that the modification with silver nanoparticles was successful, and an even distribution of silver on the silica surface with an average silver load of around 16% was determined. After silver nanoparticle modification, silica synthesized using cetyltrimethylammonium bromide as a porogen was mesoporous, whereas silica synthesis using Pluronic P123 as a porogen yielded a nonporous product. The synthesized silicas exhibited surface areas of 345 ± 2 and 8.80 ± 0.05 m²/g for samples prepared using cetyltrimethylammonium bromide and Pluronic P123 as porogens, respectively, and both silicas were stable below 250 °C. Full article

The presence of 2-methylisoborneol (2-MIB) in water is a critical global concern due to its low threshold and resistance to conventional processes. In the present study, activated carbon/alginate (AC/alginate) composite beads were synthesized via ionic gelation method for the removal of 2-MIB from aqueous solution. The physicochemical characteristics of the adsorbent were determined using scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) techniques. The effects of contact time, solution pH, initial 2-MIB concentration and adsorbent dose on adsorption were examined. Over 95% of 2-MIB removal was obtained under optimum conditions within 360 min. The adsorption equilibrium was well described by Langmuir (R² = 0.97) and Freundlich (R² = 0.96) models suggesting that 2-MIB adsorption involves both monolayer and multilayer adsorption. Kinetic modeling revealed that the pseudo-first order model showed strong fits to the experimental data, indicating the role of surface adsorption in controlling the rate of adsorption. The adsorbent demonstrated reasonable stability, retaining 59% removal efficiency after four adsorption–desorption cycles, highlighting its potential for repeated application in water treatment. Overall, the AC/alginate composite beads were found to be promising for the effective elimination of 2-MIB from water. Full article

“Lumblija” is a Croatian autochthonous sweet bread which recently obtained a European Protected Geographical Indication (PGI) label. The peculiarity of “Lumblija” is the use of ingredients such as concentrated grape must, rose or herbal brandy, and various herbs and spices, mostly produced and collected in the area of the island of Korčula. To the author’s knowledge, the volatile compounds of “Lumblija” have not been investigated till now. The aim of this study was to characterise the volatile compounds responsible for the distinctive aroma of the traditional sweet bread “Lumblija”, which is widely appreciated for its unique sensory properties. Four samples of “Lumblija” were investigated. Headspace solid-phase microextraction coupled with gas chromatography–mass spectrometry analysis (HS-SPME/GC-MS) was applied for volatile compound characterisation of “Lumblija” samples. A total of 50 volatile compounds were identified in the “Lumblija” samples. Volatile compounds belong to different chemical classes: terpenes, phenylpropanoids, alcohols, aldehydes, esters, ketones, aromatic hydrocarbons, and carboxylic acids. Among them, terpenes and phenylpropanoids were the most numerous and the most abundant volatile compounds. Most differences in the volatile compound profile of “Lumblija” samples can be attributed to some specific ingredients such as spices. The results of this study could be useful to establish a volatile compound profile of “Lumblija”, which could serve as an indicator of the authenticity and quality of this autochthonous bakery product. Full article

Biopolymers and bio-based plastics, such as polylactic acid (PLA) and polybutylene succinate (PBS), are recognized as environmentally friendly materials and are widely used, especially in the packaging industry. The purpose of this study was to assess the degradation of PLA- and PBS-based formulations in the forms of granules and films under controlled composting conditions at a laboratory scale. Biodegradation tests of bio-based materials were conducted under controlled aerobic conditions, following the standard EVS-EN ISO 14855-1:2012. Scanning electron microscopy (SEM) was performed using a high-resolution Zeiss Ultra 55 scanning electron microscope to analyze the samples. After the six-month laboratory-scale composting experiment, it was observed that the PLA-based materials degraded by 47.46–98.34%, while the PBS-based materials exhibited a final degradation degree of 34.15–80.36%. Additionally, the PLA-based compounds displayed a variable total organic carbon (TOC) content ranging from 38% to 56%. In contrast, the PBS-based compounds exhibited a more consistent TOC content, with a narrow range from 53% to 54%. These findings demonstrate that bioplastics can contribute to reducing plastic waste through controlled composting, but their degradation efficiency depends on the material composition and environmental conditions. Future efforts should optimize bioplastic formulations and composting systems while developing supportive policies for wider adoption. Full article

The Pharmaceutical Strategy for Europe addresses the environmental implications at all stages of the life cycle of pharmaceuticals, from design and production through use to disposal. In the last decade, “green chemistry” has transformed pharmaceuticals by promoting sustainability and reducing environmental impact. This review discusses the latest developments in green chemistry approaches, which are applied in drug design and production, including the concepts, innovative techniques, and methodologies. This review is notably built on over 80 documents and demonstrates the practical application of green chemistry principles in pharmaceutical synthesis, emphasizing successful implementation and the environmental benefits achieved. Therefore, this review discusses the positive changes brought by green chemistry to pharmaceutical production and highlights the need for further research in designing and manufacturing “greener” substances, as well as in pollution abatement. Full article

As the demand for environmentally friendly materials continues to rise, poly(lactic acid) (PLA) has emerged as a promising alternative to traditional plastics. The present review offers a comprehensive analysis of the biodegradation behavior of PLA in diverse environmental settings, with a specific focus on soil, compost, water, and wastewater environments. The review presents an in-depth comparison of the degradation pathways and kinetics of PLA from 1990 to 2024. As the presence of different microorganisms in diverse environments can affect the mechanism and rate of biodegradation, it should be considered with comprehensive comparisons. It is shown that the mechanism of PLA biodegradation in soil and compost is that of enzymatic degradation, while the dominant mechanisms of degradation in water and wastewater are hydrolysis and biofilm formation, respectively. PLA reveals a sequence of biodegradation rates, with compost showing the fastest degradation, followed by soil, wastewater, accelerated landfill environments, and water environments, in descending order. In addition, mathematical models of PLA degradation were reviewed here. Ultimately, the review contributes to a broader understanding of the ecological impact of PLA, facilitating informed decision-making toward a more sustainable future. Full article

Metal corrosion poses a significant challenge for industries by decreasing the lifespan of materials and escalating maintenance and replacement costs. This study is critically important, as it assesses the corrosion resistance properties of annealed steel wire electrodes coated with manganese, employing chronoamperometry and linear voltammetry techniques. The electrodes were immersed in an electrolyte solution and subjected to chronoamperometry at various voltages (−0.55 V, −0.60 V, and −0.70 V) and durations (60 s and 1800 s). Subsequently, linear voltammetry was performed over a potential range from −0.8 V to 0.8 V to generate Tafel plots. The Butler–Volmer equation was applied to the data obtained to determine the corrosion current density. The results indicate that the optimal conditions for forming a highly effective protective manganese layer occur at a potential of −0.70 V for 1800 s. Under these conditions, the electrodes exhibited superior corrosion resistance. This study also revealed that shorter durations and less negative potentials led to less-effective manganese coatings, with higher corrosion rates and reduced stability. These findings are significant for developing efficient corrosion protection methods in industrial and research applications, providing clear parameters for optimizing the manganese electrodeposition process on annealed steel. Full article