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Water adsorption energy, Eads, is a key physical quantity in sustainable chemical technologies such as (photo)electrocatalytic water splitting, water desalination, and water harvesting. In many of these applications, the electrode surface is operated outside the point (potential) of zero charge, which attracts counter-ions to form the electric double layer and controls the surface properties. Here, by applying density functional theory-based finite-field molecular dynamics simulations, we have studied the effect of water adsorption energy Eads on surface acidity and the Helmholtz capacitance of BiVO4 as an example of metal oxide electrodes with weakly chemisorbed water. This allows us to establish the effect of Eads on the coordination number, the H-bond network, and the orientation of chemisorbed water by comparing an oxide series composed of BiVO4, TiO2, and SnO2. In particular, it is found that a positive correlation exists between the degree of asymmetry ΔCH in the Helmholtz capacitance and the strength of Eads. This correlation is verified and extended further to graphene-like systems with physisorbed water, where the electric double layers (EDLs) are controlled by electronic charge rather than proton charge as in the oxide series. Therefore, this work reveals a general relationship between water adsorption energy Eads and EDLs, which is relevant to both electrochemical reactivity and the electrowetting of aqueous interfaces. [ABSTRACT FROM AUTHOR]

A compact and responsive thermoelectric photodetector is introduced for the mid‐infrared. By resonantly coupling mid‐infrared light to a Sb2Te3‐Bi2Te3 thermoelectric junction, a thermocouple is formed that is directly heated by narrow‐band mid‐infrared radiation. Near‐perfect absorption is achieved at this hot junction through the resonantly enhanced coupling of light to free‐electrons in the Bi2Te3 and Sb2Te3 materials. The fabricated devices operate at 3.6 µm and demonstrate a responsivity of 10.2 V W−1, a specific detectivity of 4.6  × 106 cm Hz1/2 W−1, and a bandwidth in the order of 1 kHz. The optimal detection wavelength can be spectrally tuned by changing the resonant cavity dimensions. This work shows a path toward miniaturized mid‐infrared detectors and spectrometers with high sensitivity, responsivity, and bandwidth. Importantly, the device presented here is ideal for industrial production, which it is hoped will provide wider access to mid‐infrared technologies for chemical sensing, medicine, and security. [ABSTRACT FROM AUTHOR]

AbstractEmerging contaminants (ECs) have become a significant threat to the aquatic environment due to their persistence and potential to harm living organisms exposed to them over extended periods. The identification of a broad range of ECs in various water bodies has accelerated research into their harmful effects and removal methods. The presence and durability of ECs, such as endocrine-disrupting substances, personal care products, pharmaceuticals, and their transformation products pose important environmental and health challenges. Traditional wastewater treatment processes often fail to eliminate ECs due to their ability to form hazardous derivatives, complexes, dynamic partitioning, and transformation products. Membrane processes have become increasingly important in pollution control, as their performance has been proven from technological, economic, energy, and environmental perspectives. This review article aims to provide a comprehensive summary of the origins and effects of ECs on humans and the environment. It discusses various membrane technologies for the efficient and ecologically responsible removal of emerging pollutants from wastewater. Reverse Osmosis (RO), Microfiltration (MF), Ultrafiltration (UF), and Nanofiltration (NF) membranes demonstrated outstanding removal efficiency for a variety of ECs; nevertheless, both methods are hindered by fouling problems. The paper highlights the methods used by hybrid membrane technology to eliminate emerging pollutants. Additionally, the use of ceramic membrane technology in removing emerging pollutants has been investigated. Ceramic membrane technology is particularly appealing due to its inherent benefits, such as chemical and thermal stability, low fouling propensity, and extended lifespan. Future research avenues for the removal of emerging pollutants using green, sustainable technologies and hybrid membranes are also presented. [ABSTRACT FROM AUTHOR]

In this study, onium‐ion‐added nanoclay (NC)/microcellular polypropylene (PP) composites were created using a conventional injection molding machine. A chemical foaming agent was utilized to facilitate mixing. The primary focus was to analyze how altering the NC content affects the mechanical characteristics and the properties of the endothermic chemical foaming agent added PP/NC composites. The composites were created using a chemical foaming agent at a weight ratio of 1 wt% and NC at weight ratios of 0 wt%, 2.5 wt% and 5 wt%. The findings indicated that an increase in the NC ratio led to higher cell count and cell density, along with a reduction in cell diameter. Additionally, the outcomes demonstrated that the foaming of PP/NC composites resulted in decreased modulus of elasticity and tensile strength while enhancing impact strength. © 2024 The Authors. Polymer International published by John Wiley & Sons Ltd on behalf of Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

In this study, we look into how poly[(4‐styrenesulfonic acid)‐co‐(4‐vinylpyridine)] crosslinked with divinylbenzene can be used as a copolymeric material to effectively recognize l‐epinephrine (L‐EP) and chirally separate (±)‐EP. It was first possible to synthesize and analyze L‐EP‐styrene‐4‐sulfonamide (L‐EP‐SSA). The resulting chiral sulfonamide was used to copolymerize with a 4‐vinylpyridine–divinylbenzene mixture. The integrated L‐EP species were removed by heating the polymer materials under strong alkaline conditions to degrade the sulfonamide links, followed by acidification in HCl solution. The imprinted L‐EP‐IP materials were analyzed using Fourier transform infrared spectroscopy and scanning electron microscopy. The produced L‐EP‐IP displayed selectivity characteristics indicative of an affinity for L‐EP almost eleven times higher than that for d‐epinephrine (D‐EP). At a pH of 7, Langmuir adsorption experiments demonstrated a maximal capacity of 165 mg g−1. Following optical separation by means of a column method, enantiomeric excess levels of L‐ and D‐EP in the initial feeding and subsequent recovering solutions were calculated to be 93% and 80%, respectively. © 2024 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

Although epoxy resin (EP) has been widely used in many fields, it is still urgent to effectively improve its flame retardancy by halogen‐free strategies. Herein, a silicon‐containing cyclotriphosphazene derivative (HEP‐Si) was synthesized by nucleophilic substitution and silicon–hydrogen addition reaction using eugenol, hexachlorophosphazene and triethylsilane as raw materials. Then it served as a halogen‐free flame retardant for an EP/4,4′‐diaminodiphenylmethane system, and its performance was compared with that of commercial flame retardant hexaphenoxycyclotriphosphazene (HPP). The results showed that although the initial thermal decomposition temperature (T5%) of the cured products of EP/HEP‐Si was slightly lower than that of pure EP, T5% did not decrease further as the amount of HEP‐Si increased, indicating that good thermal stability was maintained. In addition, the char yield of the cured products of EP/HEP‐Si was significantly increased (more than 20 wt%) compared to that of pure EP. The cured EP with the addition of HPP and HEP‐Si both achieved a V‐0 rating in UL‐94 vertical burning test at 0.5 wt% phosphorus content, while the limiting oxygen index of the EP/HEP‐Si system was higher, reaching 33.2%. From cone calorimetric test results, the peak heat release rate, total heat release and total smoke production of the cured products of EP/HEP‐Si decreased by 61.5%, 37.1% and 26.2%, respectively, compared with that of pure EP. The cured EP/HEP‐Si materials also exhibited good thermomechanical and mechanical properties. Therefore, HEP‐Si is suggested to be a promising P/N/Si‐containing halogen‐free flame retardant for EP. © 2024 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

BACKGROUND: Adsorption is a promising affinity separation technique to target a sorbate in extremely dilute solutions. In this work, methacrylonitrile (MAN)‐functionalized resins were investigated to recover volatile fatty acids (VFAs) from a mimicked fermentation broth as an alternative for the already known amine‐based resins and non‐functionalized poly(styrene‐divinylbenzene) (PS‐DVB), aiming for high VFA capacity and selectivity. RESULTS: Next to comparison with commercial PS‐DVB resin, also several PS‐DVB resins were synthesized as non‐functionalized analogues for the new MAN‐functionalized resins. For MAN‐functionalized resins, the maximum equilibrium VFA loading of about 153 (g acid/kg adsorbent) was found, which is higher than the 125 (g acid/kg adsorbent) for the PS‐DVB non‐functionalized resins. The water uptake of the PS‐DVB resins was with 0.53–0.87 (g water/g adsorbent) significantly lower than for the MAN‐DVB resins taking up 0.99–1.85 (g water/g adsorbent). CONCLUSION: Overall, the MAN‐functionalized adsorbents retained higher loading capacity for corresponding acid, compared to the PS‐DVB resins, while also taking in more water. Acid uptake is due to the hydrogen bonding between the nitrile groups of the resins with carboxyl group of the acids. Moreover, none of the adsorbents displayed an affinity towards the salts present in the fermentation broth. © 2024 The Author(s). Journal of Chemical Technology and Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry (SCI). [ABSTRACT FROM AUTHOR]

Chemistry is a highly technical field that relies heavily on a range of symbolic and imagic formalisms. These formalisms conceptualize specific chemical knowledge into semiotic resources that are rarely used elsewhere in most other academic fields or contexts. To develop an understanding of semiosis in highly technical fields such as chemistry, key questions include what this range of formalisms do and why they occur. These are key questions not only for our understanding of semiosis, but also if we wish to develop integrated literacy programs that can support students to marshal the multimodal discourse of chemistry. This paper explores these questions by examining how three key chemical formalisms organize their meaning: symbolic formalisms known as chemical formulas and chemical equations, and an imagic formalism known as structural formulas. Drawing on Systemic Functional Linguistics and using a corpus of formalisms from secondary school chemistry, these formalisms are explored in terms of their overarching grammatical organization and the content meanings they realize through the concept of "field." This is used to compare and contrast each formalism in terms of a semiotic typology so as to understand how they work and what meanings they realize. By exploring chemical formalisms in this way, this paper establishes a means of seeing the similarities and differences in meaning-making across formalisms and explaining why different formalisms occur. This then begins to provide a base upon which applied programs can interpret the literacy needs of chemistry. [ABSTRACT FROM AUTHOR]

In this work, we investigate the properties and stability of the combustion waves propagating in a system of layered solid fuel material in which the neighbouring fuel sheets can recuperate heat via thermal electromagnetic radiation. The analysis is undertaken within the flame sheet model, which allows to determine the combustion wave speed and structure and derive the dispersion relation characterising the stability of the reaction front. The proper choice of parameters leads to superadiabatic combustion temperature and significant increase of the combustion wave speed. In addition, the stable steady regimes of combustion can be substantially extended in the space of parameters. Such an enhancement of stability and ability to control the characteristics of the combustion wave propagation can be very attractive for the combustion synthesis of new layered materials, similarly to the chemical furnace technology proposed earlier. [ABSTRACT FROM AUTHOR]

This study described the chemical engineering technology to signify the utilization of non-edible Faidherbia albida seeds as a promising botanical source for biofuel production, regarding their potential to address both energy needs and environmental concerns. This research offers valuable description into sustainable fuel production technology, along with the objectives to achieve the chemical engineering to develop solutions for a more sustainable future. The utilization of non-edible F. albida as a source for biofuel production, utilized phytonanoctalyst to enhance its catalytic efficiency. F. albida seed oil concentration of 38% (w/w), non-edible feedstock presents a valuable solution for producing high-quality biofuel. The application of an innovative green nanocatalyst of calcium oxide (CaO) and Tamarindus indica pods extract proved beneficial to enhance the transesterification process. The characterization tools such as SEM, EDX, XRD, FTIR, and HPLC were performed. The verification of methyl ester synthesis was confirmed through FTIR and HPLC analysis. The average nanoparticle size was determined 25.93 nm, while the diffraction peaks elaborate the hexagonal polycrystalline structure. This research provides implications for the advancement of biofuel production, explained the vital role of this interdisciplinary catalysis approach to address the global energy challenges and paving the way for a more sustainable future. [ABSTRACT FROM AUTHOR]

Integrating flame‐retardant additives into epoxy resins is an essential strategy for improving their fire resistance. However, introducing flame‐retardant groups often compromises the processability and mechanical integrity of such resins. In this research, we synthesized a novel, biobased flame retardant, referred to as DPN, using naringenin and chlorodiphenylphosphine as precursors via a straightforward single‐step process. The addition of DPN markedly decreased the viscosity of hydantoin epoxy resin, from 7468 to 1285 mPa s. Furthermore, when cured with 4,4‐diaminodiphenylmethane, the composite containing five equivalents of DPN (DPN‐5) exhibited a marked improvement in mechanical strength, reaching 190 MPa, significantly outperforming the pure thermoset (DPN‐0: 104 MPa), while preserving high transparency. Combustion tests further confirmed that DPN significantly boosts the flame resistance of the thermoset, with DPN‐5 achieving a limiting oxygen index of 37% and securing a UL‐94 V‐0 rating. Cone calorimetry analysis showed that DPN‐5 effectively reduced heat and smoke production during combustion, achieving a 13.4% reduction in peak heat release rate and a 28.2% decrease in total heat release compared to DPN‐0. This study underscores the potential of multifunctional biobased flame retardants derived from renewable resources in advancing the development of high‐performance materials. © 2024 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

The demands of cost‐driven industrial applications can be satisfied by manufacturing composites with a low volume fraction of carbon fibres as phenolic carbon fibre‐reinforced composites and C/C composites, both with acceptable performances, for low‐ or high‐temperature applications, respectively. Polymeric composites reinforced with a low volume fraction (7.5% v/v) of carbon fibres were fabricated using laboratory‐produced phenolic resins, novolac (N) and resole (R), as matrices after different curing/post‐curing temperature profiles. By optimising the manufacturing conditions, the N‐based polymeric composites exhibited higher flexural strength, whereas the R‐based composites showed higher shear strength. C/C composites, namely N‐based and R‐based, were manufactured by pyrolysis of the previously prepared polymeric composites up to 1000 °C. The pyrolysed composites were then densified by impregnation with an appropriate resin solution, followed by curing and new pyrolysis, and particularly by employing 1 up to 4 consecutive cycles of 'impregnation–curing/pyrolysis'. Weight changes resulting from the impregnation–curing and pyrolysis stages were determined. The curing of both resins was verified by Fourier Transform Infrared Analysis. The apparent density and X‐ray diffraction data of the C/C composites were used to calculate their total percent porosities. The morphology and elemental composition of the C/C composites at their failure region (after flexural testing) were examined by Scanning Electron Microscopy/Energy‐Dispersive X‐ray Analyses. In comparison to the N‐based C/C composites, the R‐based ones exhibited: higher shear strength, lower flexural strength, higher Shore D hardness, slightly higher surface conductivity and lower volume conductivity. The optimum conditions for the manufacture of C/C composites were achieved by applying two consecutive cycles of 'pyrolysis–impregnation–pyrolysis' to the polymeric composites. © 2024 The Authors. Polymer International published by John Wiley & Sons Ltd on behalf of Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

Due to their unique properties and use in high performance materials, the ability to obtain fluorinated polymers utilizing straightforward synthetic methods remains of interest. In this study, we report the facile synthesis of new fluoropolymers via nucleophilic addition of a di‐thiol to perfluorocyclopentene. Initially, model studies were completed with perfluorocyclopentene, benzenethiol and tetramethylsilane‐protected benzenethiol to identify the optimal reaction conditions for the polymerization. These reaction conditions were then utilized to prepare perfluorocyclopentene‐thioether polymers from perfluorocyclopentene and 4,4′‐thiobisbenzenethiol. The isolated polymers had molecular weight distributions consistent with step‐growth polymers and 19F NMR spectroscopy revealed that the addition of the nucleophile to perfluorocyclopentene was controlled. Analysis by DSC showed that the polymers were amorphous with glass transition temperatures around 65 °C. TGA in both air and nitrogen showed an initial degradation temperature around 370 °C, while the air analysis produced an additional plateau with a degradation temperature near 592 °C. This is the first known report of utilizing perfluorocyclopentene for the preparation of perfluorinated‐thioether polymers. © 2024 Society of Industrial Chemistry. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA. [ABSTRACT FROM AUTHOR]

Amphiphilic block copolymers are characterized by the presence of distinct hydrophilic and hydrophobic regions, which are usually arranged in alternating blocks. This unique structure allows these copolymers to self‐assemble into well‐defined nanostructures that exhibit remarkable resistance to enzymatic hydrolysis, high biocompatibility and the ability to be customized with specific structures. These properties make them highly desirable in various applications. Self‐assembled amphiphilic polypeptoids are currently under development as a promising class of pharmaceutical agents. However, the utilization of these peptides as drug carriers for efficient delivery presents a number of challenges. These challenges include less‐than‐optimal loading efficacy and restricted biocompatibility. Herein, a series of stable amphiphilic block copolypeptoids (PNEG‐b‐PNBG and PNEG‐b‐PNHG) were designed and synthesized by controlled ring‐opening polymerization. PNEG chain segments provide hydrophilicity, while PNBG and PNHG chain segments provide hydrophobicity. The hydrophobic molecular chains aggregate in aqueous solutions, resulting in the formation of nano‐assemblies. The self‐assembled amphiphilic block polypeptoid copolymers were investigated. The morphologies of copolymers take the form of micelles from tens of nanometers to a few hundred nanometers. The properties of amphiphilic block copolypeptoids used as drug carriers were further investigated by conducting drug release and cytotoxicity tests. The results indicate that the cumulative release efficiency of self‐assembled polypeptoid copolymers can reach up to about 91%. And they have good biocompatibility and can be expected to be safe materials for efficient drug delivery. This work could provide a facile method for the preparation of amphiphilic block peptoid copolymers for biopharmaceutical applications. © 2024 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

Nowadays, there is a rising interest in the packaging industry regarding more environment‐friendly (i.e. biodegradable and/or compostable) polymer‐based solutions, especially for film blowing applications. However, replacing traditional, fossil resource‐based polymers typically used for such applications is not an easy task, since the more environment‐friendly solutions must have adequate features in terms of processability and final properties. In this work, three commercial biodegradable (and, at least partially, biobased) polymers were investigated by a preliminary rheological and mechanical analysis, in order to perform film manufacturing experiments in laboratory equipment. Furthermore, oxygen and water vapour barrier properties were studied by permeability measurements. The investigation was ultimately performed on films produced in industrial equipment, and the results were compared to those for a typical, standard polypropylene (PP) film used in flexible packaging applications. It was found that the mechanical properties were adequate (in some cases, even up to 25–30% higher than for the PP counterpart), as well as oxygen permeability. On the other hand, water permeability was significantly higher than that of PP films, and this should be taken into account in cases where high water vapour barrier properties are required. © 2024 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

Poly(ethylene terephthalate) (PET), both bottle grade (PET‐B) and thermoform grade (PET‐T), are widely used in the packaging sector. However, only PET‐B is recycled and reused, while PET‐T needs to be separated from recycled PET bales. This study aims to assess the impact of solid‐state polymerization (SSP), chain extension and the combination of chain extension–SSP to transform PET‐B and PET‐T blends into PET‐T‐like material. The intrinsic viscosity (IV) values for PET‐B blends with 10–20 wt% of PET‐T are measured for the samples obtained in this study. The mechanical properties, such as tensile strength, modulus, elongation and impact strength, were also determined. The glass transition temperature, melting temperature, crystallinity and thermal degradation were also investigated. The findings suggest that the combination of SSP and chain extension leads to a significant improvement in IV and tensile strength, while SSP alone is less suitable to offer the desired IV values. © 2024 The Authors. Polymer International published by John Wiley & Sons Ltd on behalf of Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

Graphene and its derivatives are promising energy storage devices due to their high specific surface area, chemical and thermal durability and high charge transfer power. Still, their stacking and aggregate behavior can limit their practical application. To address this issue, reversible addition–fragmentation chain‐transfer (RAFT) polymerization as controlled radical polymerization was applied to functionalize the surface of graphene oxide with poly(N,N‐dimethylaminoethyl methacrylate) (PDMAEMA) via the 'grafting from' method. This strategy enhances the distance between graphene sheets by occupying physical volume while improving effective charge transfer through tertiary amine groups participating in the doping process. X‐ray diffraction was used to determine interlayer spacing after polymer grafting, which increased from 0.28 to 1.71 nm after polymer grafting. The hybridization of materials with diverse properties was used to enhance charge transfer capability for supercapacitor applications. PDMAEMA‐functionalized graphene oxide, nano‐manganese dioxide and polyaniline were combined to create a successful nanocomposite as electrode active material. The morphological structure and chemical composition of the synthesized nanocomposite were analyzed, and its electrochemical performance was evaluated using cyclic voltammetry, galvanostatic charge–discharge and electrochemical impedance spectroscopy. The nanocomposite exhibited a maximum specific capacitance, energy density and power density of 364.72 F g−1 (at a scan rate of 50 mV s−1), 239.08 Wh kg−1 and 678.34 W kg−1, respectively. The final nanocomposite's energy storage capacity significantly increased compared to the individual components due to hybridization's synergistic impact, reducing charge transfer resistance. © 2024 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

Mankind has erected monoliths and stone structures for millennia to ensure stories and culture are passed on to future generations. In the modern era, monuments and architecture are designed with the intention of lasting several decades to hundreds of years and may utilize an arrangement of natural and synthetic materials. Choice of substrate helps ensure the longevity of these structures, but coatings are utilized to provide additional characteristics and subsequent protection to the finished product. Protective coatings come in a variety of base materials and are utilized to address specific degradation concerns. Advances in this field focus on protection of the surface while preventing any unintended damage to the substrate. This mini review summarizes the advances in protective coatings useful for historical monuments and architecture up to January 2024. © 2024 The Authors. Polymer International published by John Wiley & Sons Ltd on behalf of Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

BACKGROUND: Biodegradable polymers are gaining a reputation as demand is increasing globally. Amongst these Polyhydroxyalkanoates (PHA) are attracting market attention as a consequence of their properties similar to those of conventional plastics. PHA is a natural polyester that is stored as an intracellular carbon (C) energy reserve of bacteria. This biopolymer can be extracted and used in place of petrochemical plastic. Medium chain‐length (mcl) PHA, specifically poly hydroxybutyrate‐co‐hydroxyhexanoate P (HB‐co‐HHx) copolymer produced by Bacillus, has gained practical attention owing to its superior physicochemical properties compared to the commonly synthesized PHB homopolymer. Co‐polymer production is dependent on C sources provided in the growth medium. In the present study we have employed palm oil and palm oil effluent as C source. RESULTS: In the current study, it was observed that a significant amount of PHA and biomass was produced when the effluent was prepared at a concentration of 100% instead of water for preparing the growth medium. The production of biomass and PHA showed a range of 4.8–8and 1.5–4 g L−1, respectively. This means that the PHA yield obtained using the effluent was 50–80% of the control, whereas the control yielded only 40–50%. CONCLUSION: Palm industry waste can be used as a substrate in bioprocessing industries. Proton nuclear magnetic resonance analysis of PHA obtained herein indicates that it consists of the mcl polymer P (HB‐co‐HHx). © 2024 The Author(s). Journal of Chemical Technology and Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry (SCI). [ABSTRACT FROM AUTHOR]

BACKGROUND: The addition of conductive materials or the application of external voltage is a promising novel methodology to enhance methane production in anaerobic digesters. However, there is limited knowledge about their individual or combined effects on the anaerobic digestion of dairy wastewater. The aim of this study was to examine the effects of granular activated carbon (GAC) or magnetite addition and external voltage application, both individually and in combination, for the anaerobic digestion of real, undiluted dairy wastewater. RESULTS: The results showed that the estimated maximum methane production rate increased significantly (P < 0.05) from 143 ± 8 mL gVSadded−1 day−1 in the control reactors to 163 ± 11 mL gVSadded−1 day−1 and 166 ± 11 mL gVSadded−1 day−1 in the reactors containing GAC, with or without the combination of external voltage, respectively. The addition of GAC, in both cases, resulted in higher consumption rate of acetate, indicating a promotion of the methanogenesis step. By contrast, the application of external voltage or the addition of magnetite had no significant effect on either methane production rate nor methane yield. Moreover, the analysis of the microbial community showed that the addition of GAC resulted in the enrichment of Desulfobacterota, Methanosarcina, Candidatus Methanofastidiosum and Methanolinea. CONCLUSION: Overall, GAC addition seems a promising strategy to increase methane production in anaerobic digesters treating dairy wastewater. © 2024 The Author(s). Journal of Chemical Technology and Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry (SCI). [ABSTRACT FROM AUTHOR]

The perspectives of technological advances needed for short term energetic transition are briefly reviewed and discussed critically. In particular, the technologies for the greenhouse gas emission-free production of electrical energy, its storage and transport, the production, transport, storage and use of hydrogen, and the use of biomass derived technologies are shortly and critically reviewed. Critical aspects are emphasized. The role of chemistry, and in particular materials chemistry and engineering, in short-term developments are underlined. [ABSTRACT FROM AUTHOR]

In the process of fuel utilization, traditional combustion technologies result in the conversion of nitrogen elements in fuels into nitrogen oxides, which are released into the atmosphere, posing serious threats to the environment and human health. The chemical looping process (CLP) is an effective technology for reducing nitrogen-containing (N-containing) pollutants during fuel utilization. During the CLP, the oxygen carrier (OC) can oxidize nitrogen oxide precursors (NH3 and HCN) released from the fuel to N2, while the reduced OC can reduce nitrogen oxides to N2. The achievement of efficient nitrogen pollutant removal relies on the development of highly active oxygen carriers (OCs). This review summarizes the recent progress in the removal of nitrogen pollutants within chemical looping processes (CLPs). It delineates the formation pathways of N-containing pollutants (NH3, HCN, NO, NO2 and N2O) and highlights the performance of various OCs. The influence of reaction conditions and feedstock characteristics is also discussed. Ni-based OCs have demonstrated superior performance in the removal of N-containing pollutants, exhibiting strong oxidation capabilities and excellent catalytic properties. Moreover, iron ore, as a cost-effective and environmentally friendly feedstock, holds promise for wide-scale application. Future research should focus on further optimizing OCs strategies and refining reaction conditions to achieve more efficient and economical N-containing pollutant removal, thereby fostering the widespread application of chemical looping technology in the energy sector. [ABSTRACT FROM AUTHOR]

While the mild production of syngas (a mixture of H2 and CO) from CO2 and H2O is a promising alternative to the coal‐based chemical engineering technologies, the inert nature of CO2 molecules, unfavorable splitting pathways of H2O and unsatisfactory catalysts lead to the challenge in the difficult integration of high CO2 conversion efficiency with produced syngas with controllable H2/CO ratios in a wide range. Herein, we report an efficient plasma‐driven catalytic system for mild production of pure syngas over porous metal–organic framework (MOF) catalysts with rich confined H2O molecules, where their syngas production capacity is regulated by the in situ evolved ligand defects and the plasma‐activated intermediate species of CO2 molecules. Specially, the Cu‐based catalyst system achieves 61.9 % of CO2 conversion and the production of pure syngas with wide H2/CO ratios of 0.05 : 1–4.3 : 1. As revealed by the experimental and theoretical calculation results, the in situ dynamic structure evolution of Cu‐containing MOF catalysts favors the generation of coordinatively unsaturated metal active sites with optimized geometric and electronic characteristics, the adsorption of reactants, and the reduced energy barriers of syngas‐production potential‐determining steps of the hydrogenation of CO2 to *COOH and the protonation of H2O to *H. [ABSTRACT FROM AUTHOR]

This document is a special issue of the journal Catalysts, featuring contributions from scientists in various fields discussing the topic of catalysis on zeolites and zeolite-like materials. The articles cover a wide range of topics, including the preparation and modification of zeolite-containing catalysts for the petrochemical industry, the synthesis of micro-mesoporous materials for efficient catalysis, the development of new zeolite systems for environmental catalysis, and the synthesis and characterization of nanoscale zeolites with various applications. The contributions emphasize the potential of zeolites and zeolite-like materials as catalysts due to their unique pore structures and surface properties. [Extracted from the article]

Context: Organic halides stand as invaluable reagents with diverse applications in synthetic chemistry and various industrial processes. Despite their utility, concerns arise due to their inherent toxicity. Addressing these apprehensions, hydro-dehalogenation has emerged as a promising strategy involving the replacement of halogen atoms with hydrogen atoms to transform toxic organic halides into hydrocarbons. This study delves into the computational exploration of hydro-dehalogenation reactions of benzyl halide, mediated by frustrated Lewis pairs (FLPs), using density functional theory (DFT). The reactions entail the formation of FLP1 or FLP2 in the presence of TMP or lutidine with B(C6F5)3, respectively. This is followed by heterolytic cleavage of dihydrogen and subsequent reaction with benzyl halides. Non-covalent interaction analysis underscores the significance of π–π stacking and CH–π interactions in stabilizing transition states. Additionally, the activation strain model (ASM) dissects activation energies, revealing the substantial impact of strain energy on reaction barriers. Energy decomposition analysis (EDA) offers insights into the contributions of electrostatic, orbital, and dispersion energies to the overall attractive interaction energy. The investigation extends to hydro-dehalogenation reactions of ethyl halides, uncovering distinct mechanisms and activation barriers. This comprehensive analysis illuminates the intricacies of hydro-dehalogenation reactions, providing valuable insights into their mechanisms and paving the way for future studies in this field. Methods: Geometry optimizations were carried out at the M06-2X/def2-SVP level of theory, which was performed using the Gaussian 16 program. Solvent-corrected single-point energies were also calculated using the polarizable continuum model (PCM) at the PCM(chloroform)-M06-2X/def2-TZVP//M06-2X/def2-SVP level of theory. The Gibbs free energy correction was determined from computations performed at the M06-2X/def2-SVP level of theory. Principal interacting orbital (PIO) analysis was conducted using the NBO 6.0 software. The nature of bonding in the respective transition state (TS) structures was analyzed using atoms-in-molecules (AIM) analyses. Additionally, the presence of non-covalent interactions (NCI) was exemplified using Multiwfn software. [ABSTRACT FROM AUTHOR]

Sustainable hydrogen, produced from renewable sources such as solar or wind, plays a decisive role in driving industrial decarbonization. Among hydrogen production technologies, steam electrolysis, and solar‐driven thermochemical cycles using reducible solid oxides show promise but face challenges due to high operation temperatures. Microwave‐driven redox chemical looping enables the direct, contactless electrification of the process, reducing the operation temperature and complexity. Previous works showed that microwaves can efficiently drive reduction/water‐splitting cycles using Gd‐doped ceria at low temperatures (<250 °C), but adjustment of material properties is needed. Here, the key properties of materials are explored that affect the redox mechanism by screening a series of doped ceria materials to enhance microwave‐driven hydrogen production. Evaluation of trivalent dopants (La3+, Gd3+, Y3+, Yb3+, Er3+, and Nd3+) reveals that reduction correlates with lattice and electronic properties. The composition Ce0.9La0.1O2‐δ achieves 1.41 mL g−1, the highest hydrogen production among the studied series. Its narrower bandgap allows for reaching higher conductivity upon microwave‐driven reduction at lower temperatures, while a larger ionic lattice size boosts solid‐state oxygen diffusion. Overall, this research remarks on the critical properties of ceria‐based materials that enhance hydrogen production in microwave‐driven water‐splitting cycles, supporting the design of more efficient materials for sustainable chemical production technology. [ABSTRACT FROM AUTHOR]

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Hybridization of natural fibers with ceramic materials for reinforcing composites allows the optimization of the properties of these materials. For this reason, the present study aims to investigate physical, mechanical, water absorption, swelling and thermal properties as well as morphological characteristics of a hybrid Paederia foetida fibers–alumina powder (PFs–Al2O3)‐reinforced epoxy composite. Epoxy resin served as the matrix, while PFs and Al2O3 were employed as reinforcement. Five types of composites were fabricated using the hot‐pressing technique. The corresponding ratios of PFs:Al2O3 volume fractions (%) considered here were 0:40 (SFA), 10:30 (SFB), 20:20 (SFC), 30:10 (SFD) and 40:0 (SFE). The results reveal that the density of the hybrid PFs–Al2O3 composites decreased for increasing volume fractions of PFs: from 2.173 g cm−3 of SFA to 1.042 g cm−3 of SFE. The highest values of tensile strength (i.e. 49.085 MPa), tensile elastic modulus (i.e. 1.431 GPa) and impact strength (24 kJ m−2) were obtained for the SFD composite material with 30% volume fraction of PFs and 10% volume fraction of Al2O3: this happened because interface bonds between PFs, Al2O3 and epoxy phases achieved their optimal configuration. Overall, mechanical properties of the hybrid PFs–Al2O3‐reinforced epoxy composites were superior to those of composites reinforced only by PF fibers or only by Al2O3. Water absorption and swellability reached their maximum values at the steady state occurring after tested samples remained immersed in water for 820 h. The SFE composite reinforced only by PFs presented the highest water absorption and swelling (i.e. 6.034% and 5.81%, respectively) while for all other hybrid composites (SFD, SFC and SFB) these two quantities remained below 5%. Density and volume fraction of voids of hybrid PFs–Al2O3‐reinforced composites were consistent with the corresponding properties of the composites reinforced only by Al2O3 or PFs. SFD was also the most thermally stable material. Scanning electron microscopy observations of fractured surfaces indicated that the microstructure of the PFs–Al2O3‐reinforced epoxy composites presents several voids, fiber pullouts and transverse fibers, which together optimize the mechanical response of the composite material. Remarkably, the SFD composite material was highly competitive with the most recently developed hybrid composites employing natural reinforcements. © 2024 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

The development of self‐healing materials is an effective strategy to improve the service life of polymer materials. In this study, self‐healing waterborne fluorinated polyurethane‐acrylate (WFPUA) containing UV‐responsive coumarin groups was prepared by Pickering emulsion polymerization using modified cellulose nanocrystal as a stabilizer. The effect of double bond‐terminated waterborne polyurethane content on emulsion polymerization and latex film properties was mainly studied. Due to the dynamic reversibility of the coumarin groups and the synergistic effect of hydrogen bonds, the optimized sample (WFPUA‐30) had excellent mechanical properties and self‐healing properties. The tensile strength was 5.24 MPa and the elongation at break was 267%. The self‐healing efficiency of tensile strength and elongation at break after 6 h of repair was 86.52% and 93.20%, respectively. In addition, due to the presence of fluorine‐containing groups, the water and oil contact angles of the latex film could reach 101.7° and 82.1°, respectively. This work broadens the way for the manufacture of self‐healing and multifunctional waterborne polyurethane‐acrylates. © 2024 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

Sulfamethymidine, a commonly employed sulfonamide, is introduced into the human body through the food chain, posing a threat to human health. Consequently, the development of a rapid and efficient detection technique is imperative. In this investigation, a photoresponsive sulfamethyridiazine‐imprinted polymer was synthesized to etch a silicon core, thereby effectively addressing the limitations encountered with conventional molecularly imprinted polymers including diminished binding capacity, restricted site accessibility and sluggish binding kinetics. The photosensitive monomer utilized in the molecularly imprinted polymers is 5[(4 (methylacryloxy) phenyl) diazene] isophthalic acid, which exhibits a stimulating reaction mechanism. The N=N bond undergoes photoisomerization, transitioning between trans and cis configurations. The adsorption experiment provides additional evidence that the hollow molecularly imprinted polymers exhibit a higher adsorption capacity, achieving a value of 0.192 mmol L−1. The experiments conducted to assess selectivity and repeatability confirm that the photoresponsive molecularly imprinted polymers exhibit a high level of selectivity and favorable repeatability. Following four cycles, the adsorption rate remains consistently at 64.3%. Additionally, the recoveries of the actual samples ranged from 95.6% to 99.7%. This finding presents a novel approach to detecting the concentration of trace pollutants in intricate substrates. © 2024 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

The block structure of olefin block copolymer (OBC) elastomer gives it good elasticity and heat resistance relative to other polyolefin elastomers. However, the non‐polar nature of OBC chains limits its comprehensive properties like dyeing and toughening for polar engineering plastics. In this work, maleic anhydride (MA) and dicumyl peroxide (DCP) were selected as a typical polar monomer and a radical initiator to modify the polarity of OBC elastomer. During the melt‐grafting process, the DCP content was tuned to optimize the grafting efficiency while the MA‐to‐OBC ratio was fixed at 5 wt%. It was found that all the melt‐grafting reactions show high efficiency and can be finished in 3 min at 170 °C. With the increase of DCP content, the estimated grafting degree of OBC‐g‐MA elastomer increases from 0.40% to 1.16% along with increased gel content from 4.27% to 22.44%. A suitable grafting process was obtained with a DCP content of 3.0 wt% by balancing grafting efficiency and final mechanical properties. The optimized OBC‐g‐MA elastomer with a grafting degree of 0.92% has a mechanical strength of 17.15 MPa, a Young's modulus of 26.35 MPa, elongation of 1564% and strain recovery of 59.73%. Additionally, the contact angle test shows that polar grafting can increase surface hydrophilicity while excessive crosslinking promotes hydrophobicity. Therefore, our work has demonstrated the feasibility of the reactive melt‐grafting method to prepare OBC‐g‐MA elastomer and can also provide a processing reference for other chemical functionalization of polyolefin thermoplastic elastomers. © 2024 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

A novel smart catalyst was developed with amino‐modified thermo‐responsive poly(N‐isopropyl acrylamide) (PNIPAM) grafts on silica‐coated magnetic nanoparticles using the conventional free radical polymerization process. By this methodology, the polymer was successfully grafted mainly onto silica‐modified iron oxide nanoparticles (Fe3O4@Si). The PNIPAM‐grafted Fe3O4@Si was then subjected to ethylenediamine treatment to produce the amino‐functionalized support (Fe3O4@Si@PNIPAM‐NH2), which was subsequently modified with carboxyl functional groups by using EDTA (ethylenediaminetetraacetic acid) to create Fe3O4@Si@PNIPAM‐NH2‐EDTA. Au nanoparticles were then decorated on this support through its two amines and four carboxylates. Different methods were used to study this novel catalyst, including inductively coupled plasma, Fourier transport infrared spectroscopy, TGA, dynamic light scattering, SEM, energy‐dispersive X‐ray analysis, vibrating sample magnetometry, XRD and elemental CHN analysis. The reduction of several aryl‐nitro derivatives demonstrated a significant catalytic activity for the as‐synthesized gold catalyst (Fe3O4@Si@PNIPAM‐NH2‐EDTA‐Au). The Au catalyst can be successfully removed from the reaction components using a magnetic field and used again in eight successive reduction reactions without significant gold leaching and loss of catalytic activity. © 2024 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

Carbon fiber reinforced polyether ether ketone (CF/PEEK) composites are widely used as tribo‐materials in the aerospace and automotive industry. To amplify the industrial utilization of extrusion‐based additive manufacturing fused deposition modeling in fabricating CF/PEEK tribo‐composites, the composites' microstructure–property relationship was studied with respect to carbon fiber content varying between 5 wt% and 30 wt%. This revealed that the incorporation of carbon fibers helped enhance the mechanical strength of PEEK greatly with an optimal content of 5 wt%, at which the composite material exhibited the highest crystallinity as well as the best mechanical performance. Tribological tests indicated that CF/PEEK composites were more suitable for high speed and heavy load conditions especially for 20 wt% CF/PEEK, which was associated with the establishment of high quality transfer films covered on counter steel surfaces. The present work provides a simple and low cost way of fabricating high performance PEEK composites used as tribo‐materials. © 2024 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

Phenol–formaldehyde (phenolic) thermosets are known for excellent heat and chemical resistance, high flame retardance, and good mechanical performance. However, phenolics are also known for their high brittleness, and tendency to form voids, due to a condensation reaction forming water during curing. These voids can decrease the mechanical performance of the resultant phenolic composite and introduce undesirable performance characteristics. This work aims to develop a technique that uses high‐pressure infiltration to obtain dense phenolic matrix composites, with commercially available resin and fiber reinforcement. The high‐pressure system developed in this work is compared to a conventional low‐pressure resin infusion technique, and the porosity after each infusion is analyzed. A model of the low‐ and high‐pressure systems was developed, and the predicted time of infiltration was compared to the experimental results. The high‐pressure system had 97% less open porosity after infusion than the low‐pressure technique, suggesting that it can produce a higher‐quality and better‐performing phenolic composite than conventional techniques. Also, the mechanical test performed indicates improved performance for the high‐pressure injection with a 30.73% increase in ultimate tensile strength in comparison to low pressure, indicating better mechanical performance. © 2024 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

BACKGROUND: Batteries play a vital role in meeting global energy needs. When their life cycle concludes, improperly discarded spent batteries can pose environmental risks primarily due to their metal content. In this sense, the recycling of metals contained in spent batteries could mean a huge advantage if they are extracted and purified using environmentally friendly processes. RESULTS: In this study, the recovery of potassium (K), zinc (Zn) and manganese (Mn) from alkaline batteries was performed using a hydrometallurgical process consisting of neutral, acid and acid reductive leaching steps at room temperature and atmospheric pressure to extract K, Zn and Mn. In the neutral leaching step, 76.8 ± 3.4 (wt. %) of the K present in the spent batteries was extracted. Thus, in the acid leaching step, 90.9 ± 0.1 (wt. %) of the initial Zn and 36.7 ± 0.4 (wt. %) of the initial Mn was extracted using sulfuric acid (H2SO4) 2 M. In a subsequent acid reductive leaching step using H2SO4 2 M and oxygen peroxide (H2O2) 0.8 M as reducing agent, 8.7 ± 0.1 (wt. %) of the initial Zn and up to 49.4 ± 0.2 (wt. %) of the initial Mn were extracted. CONCLUSION: The three‐unit process led to an overall extraction of 99.6 ± 0.3 (wt. %) of Zn and 86.1 ± 0.1 (wt. %) of Mn. Regarding the latter step, the extraction was not 100% because Mn complexes which are nearly insoluble were generated. This shows that extraction of valuable minerals from industrial residues is possible by hydrometallurgical processes. © 2024 The Authors. Journal of Chemical Technology and Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry (SCI). [ABSTRACT FROM AUTHOR]

A new study from Canada has developed a process for efficiently extracting and recycling metals from used alkaline batteries. This method, called hydrometallurgy, uses aqueous solutions to extract the metals and is more cost-effective and energy-efficient than other methods. The researchers are now working on scaling up the technique for industrial use. The document also highlights various scientific studies in applied chemistry, including the conversion of carbon dioxide to carbon monoxide, the synthesis of synthetic diamonds, the growth of hydrocarbons from biogas, the reduction of CO2 to syngas and C2 hydrocarbons, the development of electronic spider silk sensors, the creation of reflective black paint for autonomous cars, the production of vanillin from ferulic acid, and the development of reversible supramolecular adhesives. Each study offers unique findings and potential applications in different fields. [Extracted from the article]

Chemistry, a vital tool for sustainable development, faces a challenge due to the lack of clear guidance on actionable steps, hindering the optimal adoption of sustainability practices across its diverse facets from discovery to implementation. This Scientific Perspective explores established frameworks and principles, proposing a conciliated set of triple E priorities anchored on Environmental, Economic, and Equity pillars for research and decision making. We outline associated metrics, crucial for quantifying impacts, classifying them according to their focus areas and scales tackled. Emphasizing catalysis as a key driver of sustainable synthesis of chemicals and materials, we exemplify how triple E priorities can practically guide the development and implementation of processes from renewables conversions to complex customized products. We summarize by proposing a roadmap for the community aimed at raising awareness, fostering academia–industry collaboration, and stimulating further advances in sustainable chemical technologies across their broad scope. [ABSTRACT FROM AUTHOR]

To control presence of ionic species in excited state of a fluorophore is quite challenging task. Herein, we report the unusual excited‐state prototropism of an important photoacid carbazole dissolved in water in presence of small amount of added ionic liquids (ILs). We have observed that the excited state prototropic equillibria of carbazole dissolved in water can be affected by the presence of small amount of added ILs. More importantly, the excited‐state prototropism of carbazole can be controlled via the acidity of added ILs. More specifically, we found that the fluorescence emission from the neutral prototropic form of carbazole can be observed even under highly basic conditions (aqueous NaOH, pH 12.6) in presence of only small amount of any of the added ILs such as 1‐butyl‐3‐methyl imidazolium tetrafluoroborate ([bmim][BF4]), 1‐butyl‐1‐methylpyrrolidinium bis(trifluromethansulphonyl)imide ([bmpyrr][Tf2N]) and 1‐butyl‐3‐methyl imidazolium hexafluorophosphate ([bmim][PF6]). The observed fluorescence emission from the neutral form of carbazole can be attributed to excited state protonation of carbazole anion by taking proton from IL cation. In a true sense, the excited state carbazole does not transfer the proton; rather takes the proton from IL cation. The observed unusual excited state protonation of carbazole anion to neutral carbazole, in the excited state even in highly basic conditions can be attributed to the presence of acidic protons with the IL cations. Herein, we reports quite unusual results where the IL assisted excited state protonation of carbazole anion occured in an exclusive manner in which proton from the IL cation exclusively protonate carbazole anion surrounded by highly alkaline media (water, pH 12.6). ILs acidity controlled excited‐state properties of important photoacids can have a wide range of chemical and biological applications and the observed results can play important roles in chemical technology to control prototropic equillibra with the help of ILs for some specific application. These observations can open new windows to attract more applications for these alternative solvent media to applications in pH and pOH jump experiments, effective photo protecting agents and chemical lasers. [ABSTRACT FROM AUTHOR]

This article provides a comprehensive analysis of the impact of detergent chemistry on exceeding planetary boundaries, specifically focusing on antimicrobial resistance, drug development, and the integrity of the biosphere. The authors emphasize the need for a holistic approach to the chemical design of detergents and identify progress and knowledge gaps related to detergent chemistry and five planetary boundaries that are currently being exceeded. The study highlights three critical challenges that need to be addressed, including the development of a climate-friendly detergent industry, aligning materialistic and social aspects in sustainable chemistry, and creating detergents that serve a purpose without harming the biosphere. The article also discusses the potential of sustainable chemistry in promoting adherence to planetary boundaries and highlights the impact of detergent chemistry on human health and the environment. It concludes by suggesting that further research is needed to understand the effects of detergent molecules and to develop detergents that minimize their impact on the biosphere. [Extracted from the article]

This article discusses the development of a practical method for Fischer indolization, a commonly used synthetic approach in chemistry. The researchers used bench-stable sodium arylhydrazine sulfonates as a substitute for arylhydrazine, which is typically used in Fischer indolization. The sodium arylhydrazine sulfonates were easily obtained from substituted anilines and could be used directly in the reaction without further purification. The method was successful in synthesizing various tetrahydrocarbazoles and tryptamine-based pharmaceutical molecules. The researchers believe that this method has potential applications in the synthesis of indole-based pharmaceutical compounds. [Extracted from the article]

This article discusses the synthesis of substituted ß-homoprolines using rhodium catalysis. ß-Homoproline is a variant of ¿-proline and is found in natural products and pharmaceuticals. The article describes the development of a new method for synthesizing ß-homoprolines, which involves the cyclization of isoxazolidin-5-ones using a rhodium catalyst. The authors demonstrate the scope and limitations of this method and discuss the downstream transformations that can be performed on the resulting ß-homoprolines. Overall, this research provides valuable insights into the synthesis and potential applications of ß-homoprolines. [Extracted from the article]

This article discusses the synthesis of highly functionalized quinolines through a novel FeIII-catalyzed domino reaction. Quinolines have been widely used in pharmaceutical compounds and have shown various biological activities, including antifungal, antibacterial, and anti-inflammatory properties. The article presents the optimization of reaction conditions and explores the scope of the developed reaction. The FeIII-catalyzed domino reaction offers a cost-effective, environmentally friendly, and greener approach to synthesizing functionalized quinolines under mild conditions. [Extracted from the article]

This article explores a new method for the dichlorination of alkenes using iron complexes as catalysts. The authors describe a photocatalytic process that utilizes iron chloride and light-induced ligand-to-metal-charge transfer to generate reactive chlorine radicals. The reaction is efficient and selective, producing 1,2-dichloride compounds that are valuable intermediates in organic synthesis. The article also investigates the mechanism of the reaction and examines the range of substrates that can be used in this iron-catalyzed photodichlorination process. [Extracted from the article]

This article explores the catalytic C–H functionalization of trimethylamine, an important intermediate in the chemical industry. Trimethylamine is often obtained as an undesired by-product, and separating it from other methylamines is challenging and expensive. The authors discuss the development of new chemical reactions that use trimethylamine as a starting material for the synthesis of valuable products, particularly those with a dimethylaminomethyl substructure commonly found in pharmaceuticals. The article reports successful reactions of trimethylamine with various compounds, offering flexible and direct methods for its functionalization. The authors highlight the efficient activation of the α-C–H bond of trimethylamine using titanium catalysts, which allows for the synthesis of various dimethylaminomethyl-substituted products. The article also mentions the successful synthesis of the antidepressant butriptyline as an example of the potential of these new reactions. The assistance of Jessica Reimer and the supply of ampoules by Kirstin Glaser, Karin Grittner, and Frank Fleischer are acknowledged. [Extracted from the article]

The article provides up-to-date information on the latest Measurement and Signature Intelligence (MASINT) technologies to face Chemical, Biological, Radiological, Nuclear and Explosive (CBRNe) threats and their advancements exploitable by Intelligence and security practitioners. The primary emphasis is on CBRNe technologies, given their central role in MASINT. The discussion encompasses cutting-edge developments that exhibit significant potential in enhancing capabilities for the identification and mitigation of CBRNe risks. In addition, the document puts forth a set of recommendations which cover essential improvements and approaches to effectively address various aspects of CBRNe Intelligence. This comprehensive exploration aims to provide readers, including Intelligence and security practitioners, with valuable insights into the evolving landscape of MASINT technologies addressing the unique challenges posed by CBRNe threats. [ABSTRACT FROM AUTHOR]

This article explores the process of enzymatic desizing of cotton fabric using fatty alcohol alkoxylate. Desizing is an important step in wet processing cotton fabrics, as it removes starch-based sizing ingredients before dyeing or printing. The study focuses on selecting a suitable surfactant to enhance the effectiveness of enzymatic desizing. Fatty alcohol ethoxylates, specifically tridecyl alcohol, are found to be effective wetting agents and emulsifiers in this process. The article provides experimental data comparing enzymatic desizing with different surfactants to the conventional acid steeping method. The results show that the ethoxylated-propoxylated (EOH) surfactant performs better in terms of desizing efficiency, absorbency, whiteness index, and bending length. The article also references several research articles on various topics related to textile processing, providing valuable insights for library patrons conducting research on these specific topics. [Extracted from the article]

Copyright of Low-Carbon Chemistry & Chemical Engineering is the property of Low-Carbon Chemistry & Chemical Engineering Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Blends of polycarbonate (PC) and poly(1,4‐cyclohexylene dimethylene terephthalate glycol) (PCTG) were synthesized using a twin‐screw extruder. Four distinct PC/PCTG blends were produced with PCTG constituting 10%, 20%, 30%, and 40% of the total weight. Comprehensive evaluations were performed to investigate their thermal properties, solvent resistance, light transmittance, mechanical characteristics, and melt flow index. Differential scanning calorimetry and thermogravimetric analysis demonstrated a single glass transition temperature in the PC/PCTG blends, indicating high compatibility. The incorporation of PCTG was observed to affect the blends' thermal stability. The data revealed a progressive increase in solvent resistance, light transmittance, and melt flow index with increasing PCTG content. The light transmittance of the blend reached 87.5%, and the melt flow index was recorded at 124.2 g (10 min)−1. Mechanical tests showed that the tensile and bending strengths were relatively stable with the addition of PCTG, but there was a noticeable reduction in notched impact strength as the proportion of PCTG increased. © 2024 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]

Towards the goal of developing renewable, biocompatible and intelligent polymer materials, natural Eucommia ulmoides gum (EUG) was modified via epoxidation and then the epoxidized EUG (EEUG) was compounded with another sustainable and biobased polymer, polylactic acid (PLA), to develop shape memory thermoplastic vulcanizates (TPVs) through reactive blending. The prepared PLA/EEUG TPVs displayed not only enhanced toughness but also greatly improved shape recovery ability, which was generated from the co‐continuous phase structure and excellent interfacial adhesion induced by in situ compatibilization during reactive blending. It is shown that dicumyl peroxide content exerted little influence on the toughness of the TPVs. However, heat‐triggered shape memory effects of the TPVs were significantly affected by the dicumyl peroxide content with a decrease in deformation ratio (Δε) from 163.51% to 128.36% and an increase in shape recovery ratio (Rr) from 73.32% to 91.93%. The findings of the present study offer an idea for the industrialization of biocompatible and smart materials for biomedical applications. © 2024 Society of Industrial Chemistry. [ABSTRACT FROM AUTHOR]