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The anti-diabetic drug metformin is one of the most widely prescribed medicines in the world. Together with its degradation product guanylurea, it is a major pharmaceutical pollutant in wastewater treatment plants and surface waters. An operon comprising two genes of the ureohydrolase family in Pseudomonas and Aminobacter species has recently been implicated in metformin degradation. However, the corresponding proteins have not been characterized. Here we show that these genes encode a Ni2+-dependent enzyme that efficiently and specifically hydrolyzes metformin to guanylurea and dimethylamine. The active enzyme is a heteromeric complex of α- and β- subunits in which only the α-subunits contain the conserved His and Asp residues for the coordination of two Ni2+ ions in the active site. A crystal structure of metformin hydrolase reveals an α2β4 stoichiometry of the hexameric complex, which is unprecedented in the ureohydrolase family. By studying a closely related but more widely distributed enzyme, we find that the putative predecessor specifically hydrolyzes dimethylguanidine instead of metformin. Our findings establish the molecular basis for metformin hydrolysis to guanylurea as the primary pathway for metformin biodegradation and provide insight into the recent evolution of ureohydrolase family proteins in response to an anthropogenic compound. The diabetes drug metformin and its degradation product guanylurea are major pharmaceutical contaminants in waste and surface water. Here, a Ni2+-dependent enzyme that hydrolysed metformin to guanylurea and its evolutionary predecessor are presented. [ABSTRACT FROM AUTHOR]

Presented herein is a switchable synthesis of naphthalenone spiroindanediones or 4‐acyl‐1‐naphthols via condition‐controlled divergent cascade reactions of aryl enaminones with diazoindanediones. When the reaction was carried out in the presence of an oxidative additive, naphthalenone spiroindanedione was formed through C(sp2)−H alkylation followed by simultaneous spiroannulation and elimination of dimethylamine. When the reaction was carried out in the presence of an acid additive, on the other hand, 4‐acyl‐1‐naphthol was formed through ring opening of the spiroindanedione moiety attacked by the in situ released dimethylamine. In addition, the reactions are suitable for gram‐scale applications and compatible with a variety of substrates. Moreover, the naphthol products allow structural elaborations and hybridization with a drug, thus further enhancing the value of this developed method. [ABSTRACT FROM AUTHOR]

Co–xCaO/g-C3N4 catalysts were prepared using incipient wetness impregnation method and applied in isophthalonitrile hydrogenation to M-xylenedimethylamine. The characterization results and experimental data indicate that introduction of CaO crates large number of basic sites and leads to electron rich Co, hence inhibits the side reaction and improves the selectivity to M-xylenedimethylamine. 10Co–2CaO/g-C3N4 gives the best catalytic performance of 100% conversion of isophthalonitrile and 95% selectivity to M-xylenedimethylamine without any alkaline additives in the reacion system. This work is valuable for the design and preparation of hydrogenation catalysts with rich basic sites and provides a green process for nitrile compounds to amine. [ABSTRACT FROM AUTHOR]

N-nitrosodimethylamine (NDMA) is a potentially carcinogenic byproduct of disinfecting drinking water. NDMA has been classified as a Group B2 carcinogen by the U.S. Environmental Protection Agency (EPA). The pathway of NDMA formation during chlorination has been proposed; however, it is still necessary to identify the most influential factor in this process. The objective of this study was to compare the factors and conditions that lead to the formation of NDMA from dimethylamine (DMA) to identify the primary factors responsible for the occurrence of this compound in drinking water. The study examined the formation of NDMA in chlorinated water under seven different conditions, considering three factors (NO2−, NO3−, and NH3). All factors were maintained at their actual concentrations in tap or surface water. The highest levels of NDMA were observed at pH 6 when NO3− and NH3 were present, with concentrations of 22.7 ng/L and 9.79 ng/L, respectively. At pH 6, NDMA levels were observed to be 22 times higher than at pH 8. Chlorine alone was not sufficient to convert DMA to NDMA within a short period of time, specifically at least 5 h, in the absence of other factors. The concentration of NDMA increased to 41.6 ng/L in the presence of NH3. After 16 h, the presence of NO3− led to a gradual increase in NDMA levels to 19.0 ng/L. However, no further increase was observed at this point. The findings suggest that NO3− and NH3 are important factors of NDMA in chlorinated drinking water. Although previous mechanisms have not given much attention to these factors, they are expected to play a significant role in the formation of nitrosamines in both natural water and drinking water. Controlling the factors or pH appeared to be crucial for managing NDMA formation, and further research on reducing N-nitrosamines is necessary. [ABSTRACT FROM AUTHOR]

2D organic–inorganic hybrid perovskites (OIHPs) are regarded as potential candidates for the advancement of multifunctional phase‐transition materials due to their ability to integrate flexible functionality and superior electronic features from both organic and inorganic components. However, the development of 2D OIHPs with dielectric switches and weak light detection capability that are crucial for high‐resolution sensing and imaging, remains challenge. Herein, a novel 2D OIHP BDADMAPb2Br7 (1, BDA = 1,4‐butanediamine and DMA = dimethylamine) is presented, featuring a 2D Dion–Jacobson (DJ) bilayered structure incorporated with secondary amine. Upon heating and cooling cycles, 1 demonstrates long‐term reversible dielectric switching properties at 328 K. Meanwhile, 1 also shows compelling semiconductor characteristics, including a low dark current of 2.87 × 10−11 A (10 V), a large switching ratio of 4 × 103, and a high detectivity of 1.3 × 1012 Jones. In addition, the photodetector based on 1 exhibits an excellent weak light detection ability of 340 nW cm−2 at 405 nm. Such a 2D OIHP demonstrates a novel platform for creating multifunctional materials and significantly promotes the development of integrated devices. [ABSTRACT FROM AUTHOR]

One effective option to minimize N-nitrosodimethylamine (NDMA) in finished drinking water is to identify and control its precursors. However, previous works to identify significant precursors use formation potential (FP) tests using high doses to assure the maximum NDMA formation rather than the NDMA formation in finished waters. In this study, we applied characteristic low treatment doses of ozone (O3)-to-dissolved organic carbon (DOC) of target compounds of 0.8 mg/mg and NH2Cl of 2.5 ± 0.2 mg Cl2/L to evaluate the NDMAFP yields of organic compounds bearing N,N-dimethylamine (DMA) and N,N-dimethylhydrazine (DMH) during preozonation and post-chloramination. The results in pH-buffered Milli-Q water showed a significant decrease from ≤ 52% to non-detectable levels in the O3-NDMAFP yields of O3-reactive precursors (i.e., DMH-like compounds) after preozonation and post-chloramination. Similarly, a significant decrease from 0.5 to 12% to nonquantifiable levels was observed for the NH2Cl-NDMAFP yields of NH2Cl-reactive precursors; however, the NH2Cl-NDMAFP yields of N,N-dimethylbenzylamine (DMBzA)-like compounds only decreased from ~ 110 to ≤ 43%, suggesting that these compounds could contribute to NH2Cl-NDMAFPs even after preozonation. The effect of the matrix in sewage-effluent and lake water samples varied and was specific for precursors; for example, the O3-NDMAFP yield of 1,1,1′,1′-tetramethyl-4,4′-(methylene-di-p-phenylene) disemicarbazide (TMDS), an important O3-reactive NDMA precursor, did not significantly decrease when tested in sewage-effluent samples. Based on the previous occurrence concentration of TMDS in sewage samples, we estimated an NDMAFP of ~ 315 ng/L. This estimate exceeds the guidance concentrations of NDMA (3–100 ng/L), highlighting the importance of TMDS and its related compounds for NDMA formation. [ABSTRACT FROM AUTHOR]

Next-generation risk assessment relies on mechanistic data from new approach methods, including transcriptome data. Various technologies, such as high-throughput targeted sequencing methods and microarray technologies based on hybridization with complementary probes, are used to determine differentially expressed genes (DEGs). The integration of data from different technologies requires a good understanding of the differences arising from the use of various technologies. To better understand the differences between the TempO-Seq platform and Affymetrix chip technology, whole-genome data for the volatile compound dimethylamine were compared. Selected DEGs were also confirmed using RTqPCR validation. Although the overlap of DEGs between TempO-Seq and Affymetrix was no higher than 37%, a comparison of the gene regulation in terms of log2fold changes revealed a very high concordance. RTqPCR confirmed the majority of DEGs from either platform in the examined dataset. Only a few conflicts were found (11%), while 22% were not confirmed, and 3% were not detected. Despite the observed differences between the two platforms, both can be validated using RTqPCR. Here we highlight some of the differences between the two platforms and discuss their applications in toxicology. [ABSTRACT FROM AUTHOR]

Selective synthesis of primary amines from nitriles is challenging in synthetic chemistry due to the possible en‐route generation of various amines and imines. Herein, we report a practical and operationally simple MOtBu‐mediated (M=Na, K) transfer hydrogenation of nitriles to the corresponding primary amines with a relatively unexplored sacrificial hydrogen source (dimethylamine borane). The strategy encompasses a broad substrate scope under transition metal‐free conditions and does not require any solvent. The mechanistic investigation was performed with the aid of control experiments and spectroscopic studies. The GC analysis of the reaction mixture exhibited the evolution of the H2 gas. Additionally, detailed computational calculations were undertaken to shed light on the possible intermediates and transition states involved during the present protocol. [ABSTRACT FROM AUTHOR]

Monomethylamine (MMA), dimethylamine (DMA), and trimethylamine (TMA) are important compounds for atmospheric key processes, e.g., new particle formation (NPF). A description of their multiphase chemical processing within atmospheric models is incomplete, but mandatory to describe their atmospheric budgets. In this study, a detailed multiphase chemistry mechanism was developed and first process model investigations were performed. The simulations focused on pristine marine conditions, where open research questions exist regarding ambient gas-phase concentrations of methylamines, particularly with regards to unexpectedly high DMA levels. The simulations reveal that TMA oxidation in cloud droplets results into DMA formation with a yield of around 87%, a missing DMA production pathway in current models. Also, it is demonstrated that about 21% and 69% of the respective DMA and TMA gas-phase oxidation proceed via autoxidation yielding HOOCH2NHCHO and HOOCH2N(CHO)CH2OOH, respectively. The discussed processes should be included into atmospheric models for advanced predictions of NPF and climate impacts. [ABSTRACT FROM AUTHOR]

α,β‐Unsaturated aldehydes are important building blocks for the synthesis of a wide range of chemicals, including polymers. The synthesis of these molecules from cheap feedstocks such as alkenes remains a scientific challenge, mainly due to the low reactivity of alkenes. Here we report a selective and metal‐free access to α,β‐unsaturated aldehydes from alkenes with formaldehyde. This reaction is catalyzed by dimethylamine and affords α,β‐unsaturated aldehydes in yields of up to 80 %. By combining Density Functional Theory (DFT) calculations and experiments, we elucidate the reaction mechanism which is based on a cascade of hydride transfer, hydrolysis and aldolization reactions. The reaction can be performed under very mild conditions (30–50 °C), in a theoretically 100 % carbon‐economical fashion, with water as the only by‐product. The reaction was successfully applied to non‐activated linear 1‐alkenes, thus opening an access to industrially relevant α,β‐unsaturated aldehydes from cheap and widely abundant chemicals at large scale. [ABSTRACT FROM AUTHOR]

Recent experiments have revealed a vital nucleation process of iodic acid (HIO 3) and iodous acid (HIO 2) under marine boundary layer conditions. However, HIO 3 –HIO 2 nucleation may not effectively drive the observed rapid new particle formation (NPF) in certain coastal regions influenced by urban air masses. Dimethylamine (DMA) is a promising basic precursor to enhance nucleation considering its strong ability to stabilize acidic clusters and the wide distribution in marine atmosphere, while its role in HIO 3 –HIO 2 nucleation remains unrevealed. Hence, a method combining quantum chemical calculations and Atmospheric Cluster Dynamics Code (ACDC) simulations was utilized to study the HIO 3 –HIO 2 –DMA nucleation process. We found that DMA can preferentially accept the proton from HIO 3 as a basic precursor in the most stable configurations of HIO 3 –HIO 2 –DMA clusters. Kinetically, the participation of DMA in the cluster formation pathways of the iodine oxoacid system could be significant at the 10 -1 to 1 pptv level of [DMA]. Furthermore, DMA can enhance the cluster formation rates of the HIO 3 –HIO 2 system in marine and polar regions near DMA sources more than 10 3 -fold. Compared to the classical nucleation mechanism, the HIO 3 –HIO 2 –DMA mechanism exhibits strong nucleation ability, worthy of consideration as a promising mechanism in marine and polar regions rich in amine sources. The newly proposed HIO 3 –HIO 2 –DMA ternary mechanism might provide an explanation for some missing fluxes of atmospheric iodine particles. [ABSTRACT FROM AUTHOR]

Exchange of B800 bacteriochlorophyll (BChl) a in light-harvesting complex 2 (LH2) is promising for a better understanding of the mechanism on intracomplex excitation energy transfer of this protein. Structural and spectroscopic properties of LH2 lacking B800 BChl a (B800-depleted LH2), which is an important intermediate protein in the B800 exchange, will be useful to tackle the energy transfer mechanism in LH2 by the B800 exchange strategy. In this study, we report a unique spectral change of B800-depleted LH2, in which the Qy absorption band of B800 BChl a is automatically recovered under neutral pH conditions. This spectral change was facilitated by factors for destabilization of LH2, namely, a detergent, lauryl dimethylamine N-oxide, and an increase in temperature. Spectral analyses in the preparation of an LH2 variant denoted as B800-recovered LH2 indicated that most BChl a that was released by decomposition of part of B800-depleted LH2 was a source of the production of B800-recovered LH2. Characterization of purified B800-recovered LH2 demonstrated that its spectroscopic and structural features was quite similar to those of native LH2. The current results indicate that the recovery of the B800 Qy band of B800-depleted LH2 originates from the combination of decomposition of part of B800-depleted LH2 and in situ reconstitution of BChl a into the B800 binding pockets of residual B800-depleted LH2, resulting in the formation of stable B800-recovered LH2. [ABSTRACT FROM AUTHOR]

Jennifer Corwin-Buell, Denise Callahan, Deborah McGrath, Kimberly Millard, Gary Mosehauer, Nitasha R Phatak Vision Care, Bausch & Lomb Incorporated, Rochester, NY, USACorrespondence: Nitasha R Phatak, Vision Care, Bausch & Lomb Incorporated, Rochester, NY, USA, Tel +1 585-413-6397, Email Nitasha.Phatak@bausch.comPurpose: This study was conducted to evaluate and compare the in vitro disinfection efficacies of six commercial lens cleaning and disinfecting products for planned replacement soft contact lenses.Methods: Disinfection efficacies of five multi-purpose solutions (MPSs) and one hydrogen peroxide solution (HPS) as control were evaluated in the presence of organic soil according to the International Organization for Standardization (ISO, Geneva, Switzerland) ISO 14729 stand-alone test protocol. The five specified compendial organisms, three bacteria (Staphylococcus aureus, Pseudomonas aeruginosa, and Serratia marcescens) and two fungi (Candida albicans and Fusarium solani) were incubated with each solution under standard conditions, after which microbes were recovered and quantified.Results: Each of the solutions evaluated met or exceeded the standard’s primary criteria (3-log reduction of bacteria and 1-log reduction of fungi) after incubation for the manufacturer-recommended soaking time, except for COMPLETE MPS, which achieved only 0.4 ± 0.1 average log reduction for C. albicans. However, differences in efficacy between the solutions were noted. Average log reduction across all microbes for Biotrue Hydration Plus (4.6 ± 0.1) was comparable to that for CLEAR CARE PLUS HPS (4.3 ± 0.1) and greater than those for OPTI-FREE puremoist (3.6 ± 0.1), OPTI-FREE Replenish (4.0 ± 0.2), ACUVUE RevitaLens (3.9 ± 0.03), and COMPLETE MPS (3.6 ± 0.1). Biotrue Hydration Plus was especially effective at reducing the population of C. albicans (4.2 ± 0.7-log reduction).Conclusion: Products marketed for planned replacement soft CL disinfection generally meet the ISO 14729 standard’s primary criteria for reducing populations of compendial organisms, with larger differences between solutions noted with C. albicans.Keywords: multi-purpose solution, MPS, hydrogen peroxide solution, HPS, disinfection, myristamidopropyl dimethylamine, MAPD, polyhexamethylene biguanide, PHMB, ISO 14729

The detection of volatile amines is necessary due to the serious toxicity hazards they pose to human skin, respiratory systems, and nervous systems. However, traditional amines detection methods require bulky equipment, high costs, and complex measurements. Herein, we report a new simple, rapid, convenient, and visual method for the detection of volatile amines based on the gas–solid reactions of tetrachloro-p-benzoquinone (TCBQ) and volatile amines. The gas–solid reactions of TCBQ with a variety of volatile amines showed a visually distinct color in a time-dependent manner. Moreover, TCBQ can be easily fabricated into simple and flexible rapid test strips for detecting and distinguishing n-propylamine from other volatile amines, including ethylamine, n-butyamine, n-pentamine, n-butyamine and dimethylamine, in less than 3 s without any equipment assistance. [ABSTRACT FROM AUTHOR]

Hydrogen-bonded organic frameworks (HOFs) are frameworks formed by organic building blocks through hydrogen bonding forces with promising applications in various fields. However, their development has been hindered by poor stability. In this work, a multiple hydrogen bond strategy with in situ generation of dimethylamine (DMA) is proposed to design robust HOFs. The protic acid HCl and Lewis acid Ag+ catalyze the cleavage of the amide C–N bond in the solvent N,N-dimethylformamide (DMF) molecules to generate dimethylamine (DMA) molecules in situ. Then, DMA molecules form multiple hydrogen bonds with dicarboxylic phenylporphyrin (DBP), and build a crystalline hydrogen-bonded organic framework (DBP-HOF), utilizing both their donor and acceptor on the N atom of each DMA molecule. Additionally, DBP's large π conjugate structure contributes to stabilizing DBP-HOF through strong π–π stacking interactions. Notably, DBP-HOF demonstrates excellent fluorescence performance for selective detection of Cu2+, as well as responsiveness towards methylene blue (MB) and indigo carmine (IC). Interestingly, each analyte elicits distinct fluorescence behavior from DBP-HOF, enabling their effective differentiation. This study holds significant implications for designing stable HOF materials and advancing their application in optical sensing. [ABSTRACT FROM AUTHOR]

The N-nitrosamine, N-nitrosodimethylamine (NDMA), is an environmental mutagen and rodent carcinogen. Small levels of NDMA have been identified as an impurity in some commonly used drugs, resulting in several product recalls. In this study, NDMA was evaluated in an OECD TG-488 compliant Muta™Mouse gene mutation assay (28-day oral dosing across seven daily doses of 0.02-4 mg/kg/day) using an integrated design that assessed mutation at the transgenic lac Z locus in various tissues and at the endogenous Pig-a gene-locus, along with micronucleus frequencies in peripheral blood. Liver pathology was determined together with NDMA exposure in blood and liver. The additivity of mutation induction was assessed by including two acute single-dose treatment groups (i.e. 5 and 10 mg/kg dose on Day 1), which represented the same total dose as two of the repeat dose treatment groups. NDMA did not induce statistically significant increases in mean lac Z mutant frequency (MF) in bone marrow, spleen, bladder, or stomach, nor in peripheral blood (Pig-a mutation or micronucleus induction) when tested up to 4 mg/kg/day. There were dose-dependent increases in mean lac Z MF in the liver, lung, and kidney following 28-day repeat dosing or in the liver and kidney after a single dose (10 mg/kg). No observed genotoxic effect levels (NOGEL) were determined for the positive repeat dose–response relationships. Mutagenicity did not exhibit simple additivity in the liver since there was a reduction in MF following NDMA repeat dosing compared with acute dosing for the same total dose. Benchmark dose modelling was used to estimate point of departure doses for NDMA mutagenicity in Muta™Mouse and rank order target organ tissue sensitivity (liver > kidney or lung). The BMD50 value for liver was 0.32 mg/kg/day following repeat dosing (confidence interval 0.21–0.46 mg/kg/day). In addition, liver toxicity was observed at doses of ≥ 1.1 mg/kg/day NDMA and correlated with systemic and target organ exposure. The integration of these results and their implications for risk assessment are discussed. [ABSTRACT FROM AUTHOR]

Since the initial 2018 recall of angiotensin receptor blockers due to unacceptable levels of mutagenic N-nitrosodimethylamine (NDMA) impurity, numerous drug products delivering diverse active pharmaceutical ingredients (APIs) have been recalled. Regulators and the industry are working together to understand and address this widescale problem. Conventional analysis of NDMA utilizes liquid or gas chromatography-based procedures that can involve complicated sample preparation and slow sample analysis. Selected ion flow tube mass spectrometry (SIFT-MS) analyses NDMA directly in the gas phase using soft chemical ionization, with an LOQ of 2 ng g−1. Through the novel application of the multiple headspace extraction (MHE) technique, NDMA was quantified directly and rapidly from the drug product without dissolution, at levels well below the regulatory acceptable intake of 96 ng day−1. A comparative analysis of recalled metformin using MHE-SIFT-MS and a conventional liquid chromatography–mass spectrometry/mass spectrometry (LC-MS/MS) method showed good agreement. Use of the novel MHE-SIFT-MS approach may enable a wider screening of drug products to be conducted, since it provides around a three-fold increase in daily sample throughput. [ABSTRACT FROM AUTHOR]

Through computational analysis we found that pentazine and hexazine, two hypothetical high-energy density materials, exhibit inherent instability due to quantum tunneling effects. This instability remains even near the absolute zero, and therefore they can be deemed as unsynthesizable. We propose substituents that could potentially stabilize pentazine, especially dimethylamine. [ABSTRACT FROM AUTHOR]

The incorporation of organic ligands via post‐device treatment is an effective strategy to improve the stability of perovskite solar cells (PSCs). Although the active area is protected by metal electrode under post‐treatment, the aggression of post‐treatment ligands into active area cannot be avoided thoroughly. Unfortunately, the size of long‐chain amines is too large, and the three‐dimensional (3D) perovskite cannot maintain its 3D perovskite structure once the cation substitution occurs during the post‐treatment. Despite that the low‐dimensional (LD) perovskites are beneficial to stability, long‐chain amines are harmful to carrier transport in PSCs. Here, we introduce dimethylamine (DMA), a slightly oversized cation that can be doped into 3D perovskite structure, for post‐device treatment to improve the efficiency and stability of PSCs. After exposure to DMA gas, the inactive area of Cs/FA/MA mixed cation perovskite device that is not covered by metal electrode is converted into LD perovskite, passivating the defects of 3D perovskite in the active region, suppressing non‐radiation recombination and ion migration. As a result, we achieved a power conversion efficiency (PCE) of 22.29 % with negligible hysteresis and better stability after DMA post‐treatment, which is much higher than that (20.40 %) of the control device. [ABSTRACT FROM AUTHOR]

The reactions of glyoxal (CHO)2) with amines in cloud processes contribute to the formation of brown carbon and oligomer particles in the atmosphere. However, their molecular mechanisms remain unknown. Herein, we investigate the ammonolysis mechanisms of glyoxal with amines at the air‐water nanodroplet interface. We identified three and two distinct pathways for the ammonolysis of glyoxal with dimethylamine and methylamine by using metadynamics simulations at the air‐water nanodroplet interface, respectively. Notably, the stepwise pathways mediated by the water dimer for the reactions of glyoxal with dimethylamine and methylamine display the lowest free energy barriers of 3.6 and 4.9 kcal ⋅ mol−1, respectively. These results showed that the air‐water nanodroplet ammonolysis reactions of glyoxal with dimethylamine and methylamine were more feasible and occurred at faster rates than the corresponding gas phase ammonolysis, the OH+(CHO)2 reaction, and the aqueous phase reaction of glyoxal, leading to the dominant removal of glyoxal. Our results provide new and important insight into the reactions between carbonyl compounds and amines, which are crucial in forming nitrogen‐containing aerosol particles. [ABSTRACT FROM AUTHOR]

Disinfection by-products (DBPs) such as chloroacetic acids (CAAs) and N-Nitrosodimethylamine (NDMA) are prevalent pollutants in surface waters, particularly with the increasing use of chlorine-based disinfectants. The entry of these DBPs into water bodies may increase accordingly, posing ecological risks to aquatic life. To assess the toxic effects of CAAs and NDMA on submerged macrophytes, Vallisneria natans was exposed to different concentrations of CAAs (1.0, 10.0, and 100.0 μg L−1) and NDMA (0.1, 1.0, and 10.0 μg L−1). A RI value of −1) showed the most significant change in SOD activity, reaching 3.57 times that of the CT group. Ultrastructural changes also revealed stress responses in leaf cells and damage to organelles. Furthermore, metabolomics provided insights into the metabolic responses induced by CAAs or NDMA in V. natans leaves, where the composition and metabolism of lipids, fatty acids, cofactors and vitamins, amino acids, nucleotides, and some antioxidants were regulated, affecting plant growth. This study provides preliminary information for the ecological risk assessment of submerged plants by complex contamination with the disinfection by-products CAA and NDMA.

Platinum catalysts with {111} surface has obvious advantages, but the control of {111} exposure usually requires surfactants which cover the surface and decrease the catalytic performance. In this paper, tetrahedral platinum nanoparticle catalysts were successfully prepared with a simple one-step hydrothermal method and their size were successfully controlled under sub-5 nm. The tetrahedral morphology was controlled through the decomposition of dimethylamine by DMF and the small size was determined by alcohol acid radical. Because of the profitable effect of the amines for the tetrahedral morphology, no surfactant was need during the preparation. The catalysis activity was assured by the tetrahedral morphology with Pt {111} exposure without the surfactant covering, and the small size further increased the number of activity sites. For HOR, the catalyst showed higher activity, stronger anti-CO poisoning performance and longer stability than those of commercial catalyst with the same platinum load. For ORR, the catalyst also showed better performances which further promoted the four-electron reaction. Our simple preparation method successfully achieved the aims of the morphology control, size control and the elimination of surfactant, which effectively assured the good catalyst performances. The simple preparation path of such good catalysts shows a great application potential. [ABSTRACT FROM AUTHOR]

Between February 2020 and January 2022, the Food and Drug Administration (FDA) recalled 281 metformin extended-release products due to the presence of N-nitrosodimethylamine (NDMA) above the acceptable daily intake (ADI, 96 ng/day). Our previous studies indicated presence of NDMA levels above ADI in both metformin immediate and extended-release products. When metformin products have NDMA impurities, it is indispensable to check for the same impurities in metformin combination products. Therefore, the objective of the present study was to evaluate in-use stability of commercial metformin combination products for NDMA. For this purpose, metformin products in combination with glyburide (GB1-GB12), glipizide (GP1-GP8), pioglitazone (P1-P3), alogliptin (A1, A2), and linagliptin (L1, L2) were repacked in pharmacy vials, stored at 30°C/75% RH for 3 months, and monitored for NDMA impurity. The NDMA level varied from 0 to 156.8 ± 32.8 ng/tablet initially and increased to 25.4 ± 5.1 to 455.0 ± 28.4 ng/tablet after 3 months of exposure to in-use condition. Initially, 18 products have NDMA level below ADI limit before exposure which decreased to 7 products (GB5, GP3, GP5, A1, A2, L1, and L2) meeting specification. In conclusion, in-use stability study provides quality and safety risk assessment of drug products where nitroso impurities are detected in the probable condition of use. [ABSTRACT FROM AUTHOR]

This study reports the analysis of diclofenac removal from aqueous solution using a novel adsorbent coating with amphoteric surface. This adsorbent coating was improved using a new amphoteric ratio to increase its performance for the removal of pharmaceuticals such as diclofenac. The adsorbent coating was formulated using acrylic polymer emulsion, smectite-based clay powder and epichlorohydrin-dimethylamine to obtain a layer form via the implementation of a facile synthesis method. In a previous study, this adsorbent coating was successful to remove cationic and anionic dyes. Therefore, this research aimed to further investigate and test its application in the removal of other emerging water pollutants like pharmaceuticals. SEM, EDX, and FTIR analyses were carried out for the characterization of this novel adsorbent. The effects of adsorbent composition, diclofenac concentration, temperature, and solution pH were studied and modeled. The best conditions to improve the diclofenac adsorption was 303 K and pH 3 where the adsorption capacity was 25.59 mg/g. Adsorption isotherms and kinetics were quantified and modeled, and the corresponding adsorption mechanism was also analyzed. Diclofenac adsorption with this novel material was exothermic and spontaneous. This alternative adsorbent is promising for diclofenac removal from industrial wastewater systems. [ABSTRACT FROM AUTHOR]

The combination of electron-deficient viologen ligands with electron-rich POMs is a typical acceptor–donor system that has recently received much attention. Under solvothermal and hydrothermal conditions, by introducing three symmetric viologen ligands into POM-based hybrid materials, we successfully constructed four POMs–viologen inorganic–organic hybrid compounds, namely (1,3-bcbpy)2·(δ-Mo8O26) (1) (1,3-bcbpy·2Cl = 1,1′-bis(3-carboxybenzyl)-4,4′-bipyridine dichloride), {CoII(1,4-bcbpy)2(H2O)2[H2(β-Mo8O26)]}·2H2O·2CH2O (2), (1,4-bcbpy)2·(δ-Mo8O26)·2H2O (3) (1,4-bcbpy·2Cl = 1,1′-bis(4-carboxybenzyl)-4,4′-bipyridine dichloride, CH2O = formaldehyde), and {CuII(1,1-pmbby)2(H2O)[H2(β-Mo8O26)2]}·5H2O·C2H7N (4) (1,1-pmbby·2Cl = 1,1′-[1,4-phenylbis(methylene)]bis-(4,4′-bipyridine)dichloride, C2H7N = dimethylamine). These four compounds exhibit different fascinating structures, especially compound 4 is a typical metal–organic framework. Compounds 1–4 exhibit good discoloration behaviors under various external stimuli. For example, compounds 1–4 showed a positive response to the irradiation from a 300 W Xe lamp. When a positive voltage was applied to the ECD based on compounds 1–4, 1/2/3/4-ECD underwent a significant color conversion. What's more, compound 4 also showed obvious discoloration results after heating. In a word, 1–4 are multifunctional discoloration materials under different external stimuli. In addition, the coated filter paper prepared based on compound 3 can be used as a new printing material medium and can be successfully applied in erasable inkless printing and dual anti-counterfeiting. [ABSTRACT FROM AUTHOR]

In order to provide atomistic details for the mechanism of the collisional dynamics of O(3P) and dimethylamine (DMA) in the triplet electronic surface, direct dynamics simulations are reported herein. The simulations are performed at the U‐HSE06/aug‐cc‐pVDZ level of theory. The results are reported for the relative collision energy of 7.8 kcal/mol. For the vibrational and rotational excitations, following temperature regimes have been considered: 200 and 10 K, respectively. Simulations reveal that the reaction can lead to two product channels in the considered energy regime: (1) 2OH + 2CH3NHCH2 and (2) 2OH + 2CH3NCH3. The computed reaction cross section for pathways 1 and 2 are as follows: 17.89 ± 0.20 Å2 and 3.28 ± 0.03 Å2, whereas the computed microcanonical reaction rate constants for pathways 1 and 2 are as follows: (4.21 ± 0.05)*10−10 and (7.72 ± 0.07)*10−11 cm3/(molecule sec). Both pathways follow direct and indirect H abstraction processes. Among the direct pathways, stripping and rebound mechanisms have been observed, whereas the indirect pathway involves formation of a post‐reaction complex having lifetime ~0.4–0.5 ps. The velocity scattering angle distribution for the reaction is dominated by scattering in the sideways (60–120 °) and backward (120–180 °) directions with some contribution from the scattering in the forward direction (0–60 °). [ABSTRACT FROM AUTHOR]

Background: The allergen responsible for cocamidopropyl betaine (CAPB) allergies has been debated. Objectives: To investigate the sensitizing agents of CAPB, the patch test positivity rates of impurities were examined in Japanese patients with CAPB‐related allergic contact dermatitis. Materials and Methods: Thirty patients with scalp dermatitis and positive patch tests for CAPB and/or lauramidopropyl betaine (LAPB) were enrolled in this study. They were patch tested with the detergents that they had been using at the time of their first visit and with the impurities dimethylaminopropylamine (DMAPA) and lauramidopropyl dimethylamine (LAPDMA). Results: The positivity rate in patch tests of the 37 detergents that the patients had been using was 78.4% (29/37). The positivity rates of DMAPA 1% pet., 1% aq. and 0.2% aq. were 32.1% (9/28), 14.3% (4/28) and 13.3% (4/30), respectively, whereas those of LAPDMA 0.1% and 0.05% were 30.0% (9/30) and 16.7% (5/30), respectively. Among the 30 patients, 6 exhibited positive results for both DMAPA and LAPDMA, 3 showed positive results for DMAPA alone and 6 produced positive results for LAPDMA alone. Conclusion: Patch tests produced an overall positivity rate for DMAPA, LAPDMA or both of 50.0% (15/30) in patients with scalp dermatitis and positive patch test results for CAPB and/or LAPB. [ABSTRACT FROM AUTHOR]

BACKGROUND: Dried and salt‐fermented fish products are important sources of N‐nitrosodimethylamine (NDMA) exposure for human. As a potent carcinogen, NDMA was frequently detected in roasted Alaska pollock fillet products (RPFs), which is among the most common fish products in China. Until now, the occurrence and development of NDMA and its precursors (nitrites, nitrates and dimethylamine) in RPFs during processing and storage were not well elucidated, and safety evaluation of this fish product is also urgently needed. RESULTS: The presence of precursors in the raw material was verified and significant increase of nitrates and nitrites during processing was observed. NDMA was found generated during pre‐drying (3.7 μg kg−1 dry basis) and roasting (14.6 μg kg−1 dry basis) process. Continuous increase in NDMA content can also be found during storage, especially at higher storage temperature. The 95th percentile of Monte Carlo simulated cancer risk (3.73 × 10−5) surpassed the WHO threshold (1.00 × 10−5) and sensitivity analysis implies the risk was mainly attributable to NDMA level in RPFs. CONCLUSION: The occurrence of NDMA in RFPs was mainly a result of endogenous factors originating in Alaska pollock during processing and storage rather than exogenous contamination, and temperature played a pivotal role. The preliminary risk assessment results suggest that long‐term consumption of RPFs would impose potential health risks for consumers. © 2023 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Metal-mediated N–H and C–H bond activation of aliphatic amines is an effective strategy for synthesizing biologically important molecules. Ln (Ln = La and Ce) atom reactions with dimethylamine are carried out in a pulsed-laser vaporization supersonic molecular beam source. A series of dehydrogenation species are observed with time-of-flight mass spectrometry, and the dehydrogenated Ln-containing species in the formula Ln(CH2NCH3) are characterized by single-photon mass-analyzed threshold ionization (MATI) spectroscopy and quantum chemical calculations. The theoretical calculations include density functional theory for both Ln species and multiconfiguration self-consistent field and quasi-degenerate perturbation theory for the Ce species. The MATI spectrum of La(CH2NCH3) consists of a single vibronic band system, which is assigned to the ionization of the doublet ground state of N-methyl-lanthanaaziridine. The MATI spectrum of Ce(CH2NCH3) displays two vibronic band systems, which are attributed to the ionization of two-pair lowest-energy spin–orbit coupling states of N-methyl-ceraaziridine. Both metallaaziridines are three-membered metallacycles and formed by the thermodynamically and kinetically favorable concerted dehydrogenation of the amino group and one of the methyl groups. [ABSTRACT FROM AUTHOR]

Recent experiment (He et al, 2021, Science) revealed a vital nucleation process of iodic acid (HIO3) and iodous acid (HIO2) under the marine boundary layer conditions. However, HIO3-HIO2 nucleation cannot effectively derive the observed rapid new particle formation (NPF) in broad marine regions. Dimethylamine (DMA) is a promising basic precursor to enhance nucleation considering its strong ability to stabilize acidic clusters and the wide distribution in marine atmosphere, while its role in HIO3-HIO2 nucleation remains unrevealed. Hence, a method combining quantum chemical calculations and Atmospheric Cluster Dynamics Code (ACDC) simulations was utilized to study the HIO3-HIO2-DMA nucleation process. We found that DMA can compete with HIO2 to accept the proton from HIO3 as a basic precursor in the most stable configurations of HIO3-HIO2-DMA clusters. DMA can significantly enhance the cluster formation rates of HIO3-HIO2 kinetically for more than 103-fold in regions with abundant amine and scarce iodine based on combined factors of high nucleation ability and high concentration of DMA. Furthermore, the iodine oxoacids nucleation enhanced by DMA may explain the sources of rapid NPF events under different conditions corresponding to multiple ocean regions, which can provide important inspirations to understand the frequent and intensive NPF events in broad marine regions. [ABSTRACT FROM AUTHOR]

N-nitrosodimethylamine (NDMA), as an emerging nitrogenous disinfection byproduct, is strictly controlled by multiple countries due to its high toxicity in drinking water. Advanced reduction processes (ARPs) are a new type of water treatment technology that can generate highly reactive reducing radicals and make environmental contaminants degrade rapidly and innocuously. In this study, a systematic investigation on the kinetics of the NDMA degradation via the chosen UV/sulfite ARP and the impacts of some key parameters of reaction system was conducted. The results indicated that the UV/sulfite ARP was an efficient and energy saving method for the reductive degradation of NDMA. A total of 94.40% of NDMA was removed using the UV/sulfite ARP, while only 45.48% of NDMA was removed via direct UV photolysis under the same reaction conditions. The degradation of NDMA via the UV/sulfite ARP followed pseudo-first-order kinetics. Increasing both the UV light intensity and sulfite dosage led to a proportional increase in the NDMA removal efficiency. The alkaline condition favored the degradation of NDMA, with the removal efficiency increasing from 21.57% to 66.79% within the initial 5 min of the reaction when the pH increased from 3 to 11. The presence of dissolved oxygen substantially decreased the removal efficiency of NDMA due to the formation of oxidizing superoxide radicals, which competed with NDMA by capturing the reducing active radicals during the reaction. An analysis of the degradation products indicated that several refractory intermediates such as dimethylamine, methylamine and nitrite were completely decomposed via the UV/sulfite ARP, and the final degradation products were formate, ammonia and nitrogen. [ABSTRACT FROM AUTHOR]

Self‐assembly exploits noncovalent interaction to offer an effective method for the fabrication of materials. For Na9[EuW10O36] ⋅ 32H2O (EuW10), the negative charges and abundant oxygen atoms on its surface provide a handle for static self‐assembly. New properties are envisioned for EuW10 aggregates which are able to display such kinetics and time‐programming characteristics, in order to satisfy more complex and intelligent application scenarios, such as DNA binding and information encryption. In this work, EuW10 coupling with stimuli‐responsive dodecyl dimethylamine oxide (C12DMAO) can generate versatile aggregates with pH‐responsive properties. We demonstrated the temporal programming of the assembly and disassembly of EuW10 nanospheres using a pH clock reaction of acid/urease hydrolysis. The pH clock reaction endows EuW10 assemblies with dynamical properties, in which the charges and fluorescence changes are coded in this system. These fluorescent assemblies provide new application in time‐programmed DNA capture and information encryption. [ABSTRACT FROM AUTHOR]

Two-dimensional (2D) materials offer great prospects in room temperature (RT) gas sensors with minimum power consumption, compared to conventional metal oxide semiconductor sensors that require high temperature operation. In this work, we prepared violet phosphorus (VP) nanosheets by optimized liquid-phase exfoliation in various solvents. A highly sensitive gas sensor has been fabricated by using the prepared VP nanosheets for detection of dimethylamine (DMA), a toxic chemical widely used in various industries. The VP sensor shows an ultrafast response time of ∼2 s and high response to DMA at RT. The sensing mechanism has been analyzed by density functional theory calculations, revealing significant electron transfer from DMA to VP. This work explores the promise of VP in low power sensors. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Food Safety & Quality is the property of Journal of Food Safety & Quality Editorial Department 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.)

N,N-Dimethylformamide (DMF) is a universal solvent with wide applications across various industries. Current industrial synthesis requires high temperature and high pressure, starting from fossil-based carbon monoxide and dimethylamine (DMA). Herein, we report a green and electrochemical strategy to produce DMF under ambient conditions through direct oxidation of trimethylamine (TMA), which is a surplus chemical in DMA manufacturing. DMF production with 80% yield and >50% faradaic efficiency was achieved in an H-cell reactor over a graphite anode, coupled with hydrogen production at the cathode. Mechanistic investigations show that the reaction occurs through two-phase oxidation and that an aminal serves as the key intermediate. To achieve continuous DMF production, we set up a membrane-electrode assembly (MEA) flow reactor (2 cm × 2 cm), achieving a DMF productivity of 25 μmol h−1 and a faradaic efficiency of 40%. To further increase the productivity, we fabricated another membrane-free flow reactor (8 cm × 9 cm), delivering a high formation rate (550 μmol h−1) with high selectivity (>90%) at a constant current of 3 A in a 100-hour test. This study offers a unique opportunity to utilize electricity to drive surplus chemical utilization under ambient conditions, contributing to the sustainability of the chemical industry in the future. [ABSTRACT FROM AUTHOR]

Methylamine has been the only simple alkylamine detected in the interstellar medium for a long time. With the recent secure and tentative detections of vinylamine and ethylamine, respectively, dimethylamine has become a promising target for searches in space. Its rotational spectrum, however, has been known only up to 45 GHz until now. Here we investigate the rotation-tunnelling spectrum of dimethylamine in selected regions between 76 and 1091 GHz using three different spectrometers in order to facilitate its detection in space. The quantum number range is extended to J  = 61 and  Ka  = 21, yielding an extensive set of accurate spectroscopic parameters. To search for dimethylamine, we refer to the spectral line survey ReMoCA carried out with the Atacama Large Millimeter/submillimeter Array towards the high-mass star-forming region Sagittarius B2(N) and a spectral line survey of the molecular cloud G+0.693–0.027 employing the IRAM 30 m and Yebes 40 m radio telescopes. We report non-detections of dimethylamine towards the hot molecular cores Sgr B2(N1S) and Sgr B2(N2b) as well as G+0.693−0.027 which imply that dimethylamine is at least 14, 4.5, and 39 times less abundant than methylamine towards these sources, respectively. The observational results are compared to computational results from a gas-grain astrochemical model. The modelled methylamine to dimethylamine ratios are compatible with the observational lower limits. However, the model produces too much ethylamine compared with methylamine which could mean that the already fairly low levels of dimethylamine in the models may also be too high. [ABSTRACT FROM AUTHOR]

Reports of aerobic biogenic methane (CH4) have generated new views about CH4 sources in nature. We examine this phenomenon in the free‐flowing Yellowstone river wherein CH4 concentrations were tracked as a function of environmental conditions, phototrophic microorganisms (using chlorophyll a, Chl a, as proxy), as well as targeted methylated amines known to be associated with this process. CH4 was positively correlated with temperature and Chl a, although diurnal measurements showed CH4 concentrations were greatest during the night and lowest during maximal solar irradiation. CH4 efflux from the river surface was greater in quiescent edge waters (71–94 μmol m−2 d) than from open flowing current (~ 57 μmol m−2 d). Attempts to increase flux by disturbing the benthic environment in the quiescent water directly below (~ 1.0 m deep) or at varying distances (0–5 m) upstream of the flux chamber failed to increase surface flux. Glycine betaine (GB), dimethylamine and methylamine (MMA) were observed throughout the summer‐long study, increasing during a period coinciding with a marked decline in Chl a, suggesting a lytic event led to their release; however, this did not correspond to increased CH4 concentrations. Spiking river water with GB or MMA yielded significantly greater CH4 than nonspiked controls, illustrating the metabolic potential of the river microbiome. In summary, this study provides evidence that: (1) phototrophic microorganisms are involved in CH4 synthesis in a river environment; (2) the river microbiome possesses the metabolic potential to convert methylated amines to CH4; and (3) river CH4 concentrations are dynamic diurnally as well as during the summer active months. [ABSTRACT FROM AUTHOR]

N-nitrosodimethylamine (NDMA) is an environmental and food contaminant, but limited data to concern whether NDMA has adverse effects on the brain. This study first determined the concentration of NDMA in foods from aquaculture markets in Shenzhen, then analyzed the effects on C57BL/6 mice and further evaluated on the urine samples of elderly Chinese residents with normal cognition (NC, n = 144), cognitive decline (CD, n = 116) and mild cognitive impairment (MCI, n = 123). The excessive rate of NDMA in foods was 3.32% (27/813), with a exceeding range of 4.78-131.00 µg/kg. Behavioral tests showed that 60 days treatment of mice with 3 mg/kg NDMA reduced cognitive performance. Cognitive impairment in human was significantly associated with sex, educational levels, length of residence in Shenzhen, household registration, passive smoking, rice, fresh vegetables, bacon products. NDMA was detected in 55.4% (212/383) of urine samples, with a median concentration of 0.23 µg/L (1.20 × 107-157.39 µg/L). The median concentration for NC, CD and MCI were 0.32, 0.27, and 0 µg/L, respectively. The urinary NDMA concentration had a strong negative correlation with cognitive impairment (Kendall's Tau-b = -0.89, P = 0.024). The median estimated daily intake (EDI) of NDMA was determined to be 6.63 ng/kg-bw/day. Taken together, there appears to be an association between NDMA and human and murine cognition, which provides a new clue to Alzheimer's disease (AD). [ABSTRACT FROM AUTHOR]

Changes in serum concentration of methylarginines and amino acids after exercise are well documented, whereas the effects of exercise applied together with fasting are still debated and not thoroughly studied. Thus, we hypothesised that alterations in methylarginines such as ADMA, SDMA and L-NMMA might be responsible for decreased exercise performance after 8 days of fasting. Additionally, we propose that conditions in which the human body is exposed to prolonged fasting for more than a week elicit a distinctly different response to exercise than after overnight fasting. A group of 10 healthy men with previous fasting experience participated in the study. The exercise test was performed until exhaustion with a gradually increasing intensity before and after the 8-day fast. Blood samples were collected before and immediately after exercise. ADMA, SDMA, L-NMMA, dimethylamine and amino acids were analysed in serum samples by ID-LC-MS/MS. SDMA, L-NMMA and dimethylamine significantly decreased after 8 days of fasting, whereas ADMA did not change. BCAA, Phe, alanine and some other amino acids increased after fasting. Exercise-induced changes in amino acids were distinct after an 8-day fast compared to overnight fasting. A decrease in physical performance accompanied all of these alterations. In conclusion, our data indicate that neither methyl-arginine changes nor the Trp/BCAA ratio can explain exercise-induced fatigue after fasting. However, the observed decrease in hArg concentration suggests the limited synthesis of creatine, possibly contributing to reduced physical performance. [ABSTRACT FROM AUTHOR]

The goal of this study is to reveal the time dynamics of studies systematically and comprehensively on drinking water treatment and disinfection, as well as the situation in the literature, by using the bibliometric analysis method to examine scientific publications in the field of "Disinfection By-Products" between 2001 and 2022. The data gathered from the investigated articles is shown using the visual mapping approach. In this regard, the research provides for an evaluation of the disinfection by-products literature. The study's database contained 115 scientific papers retrieved from Web of Science. Istanbul Technical University is the most productive university with 23 published articles on Disinfection By-products, followed by Suleyman Demirel University with 18 published articles. Trihalomethanes, haloacetic acids are the most studied types of carbonaceous disinfection by-products in published articles, and N-nitrosodimethylamine is one of the most widely published nitrogenous disinfection by-products. The precursors of disinfection by-products or the removal of disinfection by-products are the two main focuses of the purpose of all studies. Coagulation, advanced oxidation processes and membrane processes constitute the methods used in the control of disinfection by-products. Brominated, and nitrogenous DBPs have attracted much attention due to their high toxicity. Future studies on disinfection by-products should focus on water quality standards, precursor controls, toxicity, and health effects. The necessity of bibliometric analysis of disinfection by-products is a necessity to fill the existing knowledge gaps in global and regional studies. [ABSTRACT FROM AUTHOR]

As one of the least understood aerosol processes, nucleation can be a dominant source of atmospheric aerosols. Sulfuric acid (SA)-amine binary nucleation with dimethylamine (DMA) has been recognized as a governing mechanism in the polluted continental boundary layer. Here we demonstrate the importance of trimethylamine (TMA) for nucleation in the complex atmosphere and propose a molecular-level SA-DMA-TMA ternary nucleation mechanism as an improvement upon the conventional binary mechanism. Using the proposed mechanism, we could connect the gaseous amines to the SA-amine cluster signals measured in the atmosphere of urban Beijing. Results show that TMA can accelerate the SA-DMA-based new particle formation in Beijing by 50–100%. Considering the global abundance of TMA and DMA, our findings imply comparable importance of TMA and DMA to nucleation in the polluted continental boundary layer, with probably higher contributions from TMA in polluted rural environments and future urban environments with controlled DMA emissions. [ABSTRACT FROM AUTHOR]

The widespread presence of volatile organic compounds (VOCs) is a threat to human health and environmental air quality. Dimethylamine is a highly toxic amine, which can directly affect the human respiratory system. To eliminate health risks, dimethylamine gas sensors are essential. Higher operating temperatures and poor selectivity inhibit binary metal oxides as sensing elements. In this work, inverse spinel cobalt tin oxide (Co2SnO4) thin films were deposited by the chemical spray pyrolysis method. Various phases have been addressed by the annealing conditions. Interestingly, the ordered inverse spinel turns into a disordered spinel by increasing the annealing temperature. All films were subjected to dimethylamine sensing, and the ordered inverse spinel porous nanograin Co2SnO4 thin films showed an excellent gas response of 193.53 ± 2.7 standard deviations at 100 ppm at room temperature, which demonstrates its potential use as a dimethylamine gas sensor. [ABSTRACT FROM AUTHOR]

The interaction of tris-dibenzoylmethanate Eu(III) with dimethylamine and ammonia vapors was investigated. It was found that when vapors of aqueous solutions of analytes are exposed to tris-dibenzoylmethanate Eu(III) impregnated into the SiO2 matrix, an optical response is observed in the form of an increase in the luminescence intensity of Eu(III). Changes in the luminescence spectra and luminescence excitation of this sensor are analyzed, both under the quenching action of water vapor and under the sensitizing action of analyte vapors. The main points recorded in the excitation spectra are noted, which are important for understanding the processes occurring in the near environment of the lanthanide center. The luminescent chemosensor is promising for creating sensors for detecting ammonia and amines in food safety control and environmental monitoring. [ABSTRACT FROM AUTHOR]

BackgroundN-nitrosodimethylamine (NDMA), a new disinfection by-product in drinking water, has attracted extensive attention due to its high detection rate and concentration. ObjectiveTo investigate the concentration of NDMA in drinking water in Nanjing situated in the lower Yangtze River Basin of China, and to evaluate associated human health risk. MethodsIn dry period (January–March) and wet period (July–September) of 2021, raw water, finished water, and tap water from 16 centralized water treatment plants in Nanjing were collected to detect the concentration of NDMA in water samples by solid phase extraction and gas chromatography-triple quadrupole mass spectrometry with programmable temperature vaporizer-based large volume injection. The concentrations of NDMA in water samples of different water types, water periods, and disinfection methods were analyzed, and the daily exposure levels and carcinogenic risk values of NDMA in drinking water of different exposure routes and different exposed populations were calculated. Monte Carlo simulation was implemented with Crystal Ball 11 software to establish a health risk assessment model and conduct sensitivity analysis. ResultsA total of 61 drinking water samples were collected in Nanjing, and NDMA was positive in all the water samples, with concentrations ranging from 1.36 to 25.65 ng·L−1 and an overall average concentration of (8.00±4.06) ng·L−1. There were no statistically significant differences in the average concentrations of NDMA among raw water, finished water, and tap water samples (F=2.875, P=0.064), between wet season and dry season (t=−0.855, P=0.397), or among different disinfection methods by liquid chlorine, sodium hypochlorite, and chlorine dioxide (F=0.977, P=0.385). The results of health risk assessment showed that the average carcinogenic risk of NDMA and its P95 were 5.95×10−6 and 1.12×10−5 respectively for oral intake of drinking water, and the values for dermal contact were both lower than 1.00×10−6. The mean carcinogenic risks of exposure to drinking water NDMA in children, adolescents, and adults were 1.84×10−6, 8.27×10−7, and 3.28×10−6, respectively. The results of sensitivity analysis showed that the contributions of daily drinking water volume and NDMA concentration in drinking water to the calculated health risk were high, and the contribution of body weight was negative. ConclusionThere is a potential carcinogenic risk of NDMA in the drinking water of Nanjing section of the lower Yangtze River Basin，but it is within the acceptable range.

This study was conducted with the aim of determining the effects of different black garlic (BG) levels (1%, 2% and 3%) on quality characteristics of a semi-dry fermented sausage (heat-treated sucuk). In addition, the effect of cooking time (0, 1 or 3 min at 180 °C on a hot plate) on nitrosamine formation was investigated. Fresh garlic (FG, 1%) was evaluated as the control group. BG (2% and 3%) caused a reduction in the count of lactic acid bacteria while leading to an increase in pH. FG1% gave the highest number of Micrococcus/Staphylococcus, as well as aw value. The thiobarbituric acid reactive substance (TBARS) value increased with increasing BG levels. FG (1%) showed the highest residual nitrite amount (p < 0.05). The scores for color, taste and general acceptability were reduced by the use of BG (p < 0.05). No significant difference was observed between the garlic treatments in terms of N-Nitrosodimethylamine (NDMA) and N-Nitrosodiethylamine (NDEA) when no additional cooking was applied. Cooking time was determined to have no significant effect on NDMA in 3% BG. The use of BG caused an increase in N-Nitrosopiperidine (NPIP) (p < 0.05). As for PCA, a closer correlation between NPIP and the groups containing BG was observed, while there was a strong correlation between NDMA and the FG group cooked for 3 min. The use of BG caused an increase in NPIP, but affected NDMA and NDEA depending on the cooking time. [ABSTRACT FROM AUTHOR]

Copyright of SDU Journal of Health Science Institute / SDÜ Saglik Bilimleri Enstitüsü Dergisi is the property of Suleyman Demirel University, Health Sciences Institute 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.)

Herein, the results of in‐situ synthesis of four different metal(0) nanoparticles (Pd, Cu, Ru, and Ni) loaded on the surface of cellulose (MNPs@Cellulose) separately and their catalytic use in the solventless dimethylamine‐borane (DMAB) dehydrogenation at 35.0±0.1 °C are reported. Based on the detailed kinetic studies on the solventless DMAB dehydrogenation catalyzed using MNPs@Cellulose, the following results were obtained: (i) Optimum metal loading percentage on the surface of cellulose was determined for Pd@Cellulose to be 4.0 wt.%Pd (152.39 h−1), Ni@Cellulose to be 3.0 wt.%Ni (59.09 h−1), Cu@Cellulose to be 3.0 wt.%Cu (55.45 h−1) and Ru@Cellulose to be 4.0 wt.%Ru (46.06 h−1) and by determining total turnover frequency values in average 10th minutes (TOF10), which provided the highest catalytic activity. (ii) The optimum amount of cellulose for each metal was found to be 50.0 mg for Pd, Cu, and Ru, and 40.0 mg for Ni. (iii) The Arrhenius activation energies were determined for each metal nanoparticles and calculated to be 69±2, 34±2, 35±2 and 42±2 kj.mol−1 for Pd@Cellulose, Ni@Cellulose, Cu@Cellulose, and Ru@Cellulose, respectively. [ABSTRACT FROM AUTHOR]

In the current global energy crisis, the value of hydrogen has become better appreciated. Metal borohydrides attract a lot of attention from researchers because they are rich in hydrogen. In this study, glass microscope slides were coated with nickel as nanorods for use as a catalyst by the magnetron sputtering method, and then catalytic hydrolysis reactions of dimethylamine borane and lithium borohydride were carried out to produce hydrogen. Parameters such as temperature, the amount of catalyst, lithium borohydride, or dimethylamine borane concentration were varied and their effects on the catalytic performances of the catalyst were examined. Moreover, the catalyst was characterized by field emission scanning electron microscopy and X-ray diffraction, and hydrolysis products were analyzed through field emission scanning electron microscopy with energy dispersive spectroscopy analyses. Reaction kinetic parameters were also determined. The activation energy values of dimethylamine borane and lithium borohydride were determined to be 40.0 kJ mol−1 and 63.74 kJ mol−1, respectively. Activation enthalpy values were also calculated as 37.34 kJ mol−1 and 62.45 kJ mol−1 for dimethylamine borane and lithium borohydride, respectively. Initial hydrogen production rates under different conditions were also investigated in the study. For both hydrolysis systems, the fastest hydrogen production rates were calculated as 109 mL gNi−1 min−1 and 103 mL gNi−1 min−1 for dimethylamine borane and lithium borohydride, respectively, in the experiment performed at 60 °C at 0.2 M substrate concentration and with 1.3 g of catalyst. These hydrolysis systems using this catalyst are good candidates for systems that need hydrogen. [ABSTRACT FROM AUTHOR]