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SCIENCE OF THE TOTAL ENVIRONMENT · 2023 · IF 9.8

The elevated toxicity of the biodegradation product (guanylurea) from metformin and the antagonistic pattern recognition of combined toxicity: Insight from the pharmaceutical risk assessment and the simulated wastewater treatment

Fan Gao,Hao Wen,Sen Feng,Meng Li,Lingyun Zhu,Yongzhi Zhang,Yilong Xi,Xianling Xiang

The emerging contaminants metformin (MET) and its degradation product guanylurea (GUA) are released into aquatic environments through wastewater treatment plants (WWTPs). Thus, the environmental risks of wastewater with more treatments may be underestimated due to the lower effect concentration of GUA and the higher detected concentration of GUA in treated wastewater in comparison with MET. In this study, we aimed to investigate the combined toxicity mode of MET and GUA to Brachionus calyciflorus by simulating the degrees of wastewater treatments through adjustments to the ratio of MET and GUA in medium. The results showed that the 24 h-LC 50 of MET, GUA, their mixtures of equal concentrations and the mixtures of equal toxic units to B. calyciflorus were 907.44, 544.53, 1185.82 and 940.52 mg/L, respectively, demonstrating GUA is significantly more toxic than MET. An antagonistic interaction between MET and GUA was found in mixture toxicity assessments. Compared with the control, MET treatments only significantly affected the intrinsic rate of population increase of rotifers (r m ), while all life-table parameters were significantly affected by GUA. In addition, at medium and high concentrations (120 and 600 μmol/L), the net reproductive rate (R 0 ) and r m of rotifers under GUA were significantly lower than those under MET. Notably, increased proportion of GUA relative to MET in binary-mixture treatments resulted in increased survival risk and reduced fecundity of rotifers. Moreover, the responses of population dynamics to exposures of MET and GUA were mainly attributed to the reproduction of rotifer, indicating that an improved wastewater treatment process is necessary to protect aquatic ecosystems . The study highlights the importance of considering the combined toxicity of emerging contaminants and degradation product in environmental risk assessment , especially the unintentional transformations of parent compound in treated wastewater.

CAS / MDL: 591-01-5
研究领域: 环境科学 · 毒理学
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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

3D-printed bioinspired Al2O3/polyurea dual-phase architecture with high robustness, energy absorption, and cyclic life

Xueqin Zhang,Qiaoyu Meng,Keqiang Zhang,Rongqi Zhu,Zhaoliang Qu,Ying Li,Rujie He

Ceramics are attractive for structural components because of their excellent load-bearing capacity. Nevertheless, inferior energy-absorbing ability and poor reliability under common quasi-static and dynamic environments, especially under cyclic loading, extremely limit the popularization of ceramic components. The coupling between cellular structures inspired by the light but strong porous trabeculae and core–shell structure in strong and tough natural materials provides a solution for strengthening the load-bearing capacity, energy absorption ability, and cyclic life of ceramic components. Here, we proposed a bioinspired cellular ceramic structure/polyurea (CCS/polyurea) dual-phase architecture via additive manufacturing and simple infiltration technologies. It was demonstrated that the specific load-bearing capacity and energy-absorbing ability of bioinspired CCS/polyurea dual-phase architecture under quasi-static compressive loading were 2.22 and 50.34 times of CCS, respectively. Significantly, it could be repeatedly loaded at 40.28 and 48.82 MPa for over 120 and 8 cycles, respectively. Furthermore, CCS/polyurea dual-phase architecture performed extraordinary cyclic life under dynamic loading. The cyclic lives of CCS/polyurea dual-phase architecture at impact speeds of ∼ 6 and ∼ 12 m/s reached as high as 11 and 2, respectively. This research provides a credible approach to building ceramic-based materials with extraordinary load-bearing capacity, energy absorption ability, and especially remarkable cyclic life.

研究领域: 材料科学 · 仿生学
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Agronomy-Basel · 2023 ·Vol. 13 ·期 10 ·2641 · IF 3.7

Synthesis and Application of Modified Lignin Polyurea Binder for Manufacturing a Controlled-Release Potassium Fertilizer

Mingyang Li,Gaoyang E,Conghui Wang,Ruolin Shi,Junxi Wang,Shuo Wang,Yu Wang,Qi Chen,Zeli Li,Zhiguang Liu

Conventional potassium chloride granules have inefficient applications in agricultural production due to particle irregularity and low fluidity. The application of controlled-release potassium chloride could increase the potassium-use efficiency and alleviate the shortage of potassium ore resources. In this study, a well-rounded potassium chloride fertilizer core was prepared, using the graft modification of polyurea to enhance the coating rate and release performance. The adhesive and tensile characteristics of the modified polyurea binder, as well as the granule properties of modified polyurea binder potassium chloride, were studied to determine the ideal lignin-grafted ratio. The effect of the modified polyurea binder with potassium chloride on the properties of coated fertilizer was investigated. The findings, shown by radar maps of the binder’s properties, demonstrated that the ideal mass ratio of the modified lignin polyurea binder to urea is 1:2. The Fourier-transform infrared spectroscopy results demonstrated that the amino functional groups of lignin were enhanced, improving the product’s interfacial compatibility with the polyurea matrix. Compared to humic acid (HA; 12%) and bentonite (Ben; 30%) treatments, the granule intensity of the 9.9%—1:2 treatment considerably increased by 139.10% and 38.86%, respectively, while the static angle of the granules reduced by 16.67% and 3.81%. The 28-day cumulative release rate of the modified polyurea (9.9%—2:1) with a 5% coating thickness was the lowest (28%), 42% lower than that of the lowest conventional treatment. In summary, the creation of a bio-lignin polyurea binder under the optimum conditions reduced the need for petrochemical-based materials, allowed the preparation of fertilizer with granules of increased fluidity, and enabled the successful coating of a high-salt potassium fertilizer, offering a novel technique for the high-value application of potash fertilizer coating.Keywords:lignin;modified polyurea;binder;potassium chloride;controlled-release fertilizer

研究领域: 农业科学 · 材料科学 · 化学工程
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JOURNAL OF MOLECULAR LIQUIDS · 2022 · IF 6.633

Selective coordination behaviors of Uranium(VI) with novel asymmetrical tetra-alkylcarbamides

Qi Chen,Baole Li,Junli Wang,Haowei Zhu,Xiwen Chen,Yifu Hu,Jia Zhou,Wentao Wang,Weifang Zheng,Taihong Yan

In this work, the solvent extraction and complexation behaviors of U(VI) by two novel asymmetrical tetra-alkylcarbamides, N,N’-butyl-N,N’-hexylurea ( L1 : SBHU ) and N,N’-butyl-N,N’-pentylurea ( L2 : SBPU ) in HNO 3 media were systematically investigated. Both two ligands extract U(VI) more effectively than other metals such as Pu(IV), Np(IV), and Th(IV) in a wide range of acidity. Under 5 mol/L HNO 3 , D U reached 5.25, while D Pu  = 1.08, D Np  = 0.11, D Th  = 0.13.. Additionally, no third-phase was present by the extraction of highly uranium concentration solution with SBHU even under 7 mol/L HNO 3 after four cycles demonstrating good acid resistance and resistance to the formation of the third phase. Slope analyses and FT-IR indicate that the U(VI) complexes are a form of UO 2 (NO 3 ) 2 ·2 L for the two ligands during the extraction. Additionally, based on the DFT calculations, the NBO analysis, and topological analysis were analyzed in detail. The results demonstrate that the interactions between ligands and U(VI) are shown mainly as ionic characteristics, and the ligand-to-metal charge transfer was also observed. This study enriches the coordination chemistry of actinides: Th(IV), U(VI), Np(IV), Am(III), and Pu(IV) by tetra-alkylcarbamides, which may shed light on the design and synthesis of novel U(VI) selective ligands.

研究领域: 配位化学 · 锕系元素化学 · 溶剂萃取 · 理论化学
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NEW JOURNAL OF CHEMISTRY · 2020 ·Vol. 44 ·期 27 ·11739-11745 · IF 3.288

Robust superhydrophobic polyurea@cellulose nanocrystal coating

Xinfeng Wang,Xuelian Gou,Zhiguang Guo

More and more attention has been paid to the fabrication of superhydrophobic polymeric coatings recently, which have enormous potential in the field of waterproofing and self-cleaning applications. In this work, polyurea (PU) particles were firstly prepared through the condensation polymerization between isophorone isocyanate (IPDI) and water. By the combination of cellulose nanocrystals (CNC), polyurea@cellulose nanocrystal (PU@CNC) particles were successfully fabricated. After modification with 1H,1H,2H,2H-perfluorodecyltrichlorosilane (PFDTS), superhydrophobic PU@CNC particles were obtained. Then, after adding fluorocarbon lacquer, a superhydrophobic PU@CNC coated surface was fabricated with the assistance of a spraying method. The as-prepared PU@CNC coating exhibited best liquid repellency when the mass ratio of IPDI and CNC was approximately 1/10. Furthermore, favorable mechanical durability was confirmed by the abrasion test. The results showed that the water contact angles on the PU@CNC coated surface remained above 152° and sliding angles were less than 5° even after 200 abrasion cycles. All these results indicate that the coating is suitable for widespread practical applications.

研究领域: 材料科学 · 化学工程
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JOURNAL OF APPLIED POLYMER SCIENCE · 2021 ·Vol. 138 ·期 38 ·50971 · IF 3.125

Influence of fluorine-containing side chain on the properties of waterborne polyurethane-urea

Yanqing Zhao,Yingli Su,Wangcai Zou,Gang Chen,Yiqing Deng,Jun Cheng,Haisheng Ren,Qiang Zhao

In order to prepare waterborne polyurethane with excellent water resistance and thermodynamic properties, a series of side chain fluorinated waterborne polyurethane-urea (FWPU-UA) was synthesized with polytetramethylene ether glycol, N -(2-methyl-1,3-propanediol-2′-)-perfluoro-1-butanesulfonyl amine (NPBA), isophorone diisocyanate, and isophoronediamine. With the increase of NPBA content, the weight loss temperature, glass transition temperature, and tensile strength of FWPU-UA were all improved. Gaussian fitting analysis of infrared data and density functional theory simulation proved that the introduction of fluorine side chains increased the interaction of hydrogen bonding in the FWPU-UA. X-ray photoelectron spectroscopy analysis indicated that the aggregation of fluorine atoms on the surface of film were caused by the migration and enrichment of fluorine side chains. Furthermore, the water resistance of polyurethane-urea film could be significantly improved by adding a small amount of NPBA, and the seven-day water absorption rate of polyurethane-urea film was reduced from 30.13% to 12.55%.

研究领域: 材料科学 · 化学工程
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Energetic Materials Frontiers · 2023 · IF 0

Improving the mechanical performances of polymer bonded explosives using monomer tuned polythioureas

Shao-cong Deng,Ya-jun Luo,Yan-zhou Qu,Xin-ru Yang,Zhi-jian Yang,Xu Zhao,Yi-ding Liu,Fu-de Nie

To improve the mechanical properties of 2,4,6-trinitrobenzene-1,3,5-triamine (TATB)-based polymer bonded explosives (PBXs), four kinds of polythiourea binders, namely the polyetherthiourea (P1), aliphatic polythiourea (P2), aromatic polythiourea (P3) and silane polythiourea (P4), were prepared and used in the PBXs. These four polythioureas were synthesized via the copolymerization of carbon disulfide (CS 2 ) and diamines with various structures under mild conditions. They were then characterized using nuclear magnetic resonance (NMR) and Fourier-transform infrared spectroscopy (FTIR). The interfacial binding energy between polythioureas and TATB was calculated via molecular dynamics simulations. The tensile and compression mechanical properties of various PBXs (PBX-P n , n  ​= ​1–4) were studied through Brazilian and compression tests and were then compared with those of the PBX with a conventional fluoro polymer binder (PBX-FP). The results show that the PBX-P1 possessed the strongest interfacial interaction energy and the best mechanical properties among all the prepared PBXs. Its Brazilian strength and strain was 11.0 ​MPa and 0.56%, which was 89% and 256% higher than those of the PBX-FP with the same binder proportion, respectively. Furthermore, PBX-P1 showed excellent compression mechanical properties, with a compression strength of 40.7 ​MPa and a compression strain of 3.53%. Moreover, its Brazilian and compression fracture energy was 600% and 101% higher than those of PBX-FP, respectively, which was beneficial for improving the PBX stability. The results of this study provide a new idea for designing TATB-based PBX with improved mechanical properties using polyetherthiourea binders.

研究领域: 材料科学 · 爆炸物工程 · 高分子化学
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Journal of Environmental Chemical Engineering · 2025 · IF 7.2

Selective lithium extraction from spent LiNixCoyMnzO2 powder based on S, N synergistic assisted subcritical water system

Yanxi Chen,Fanyun Su,Yuqing Rang,Guangli Liu,Xinxing Xu,Yayun Ma,Jingjing Tang,Xiangyang Zhou,Juan Yang

With the explosive growth in demand for lithium-ion batteries (LIBs), the recycling of the valuable metal components in them has become particularly important. However, in the previous recycling of spent LIBs, lithium is easily lost resulting in wasted resources. In this paper, a new simple and efficient selective lithium extraction strategy is developed, which uses a thiourea-assisted subcritical water system to achieve preferential extraction of lithium from spent LIBs. Due to the enhancement of the lithium extraction process by subcritical water and the synergistic effect of S and N in thiourea on the spent LiNi x Co y Mn z O 2 (NCM) cathode powder, 99.9% of lithium is selectively leached into water. Meanwhile, the transition metals (Ni, Co and Mn) in the leaching residue can be leached out by dilute acid, and the corresponding leaching rates are 99.8%, 99.7%, and 99.9%, respectively. In addition, LiNi 0.5 Co 0.2 Mn 0.3 O 2 (NCM523) cathode material with good electrochemical performance is successfully regenerated. The process has been economically and environmentally assessed as greatly simplifying the recycling process and establishing a highly efficient recycling route for spent LIBs with low environmental impact.

研究领域: 环境科学 · 材料科学
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Desalination and Water Treatment · 2024 · IF 1

Co-adsorption of tetracycline and copper by the thiourea-modified porous sodium alginate microspheres

Hong-yan Wu,Wen-kai Wu,Bo Chen,Qiao-ping Kong,Jian-jun Lian

The gradual increase of antibiotics and heavy metals in aquatic environments poses a serious threat to human health and ecosystems, and finding effective methods for simultaneous removal of antibiotics and heavy metals has attracted increasing concern. In this study, a novel porous structure of thiourea-modified sodium alginate microspheres (UA-Ca) was synthesized by modification with thiourea, epichlorohydrin, and calcium chloride, and was applied for the simultaneous removal of tetracycline (TC) and Cu(II) from water. The results indicated that the UA-Ca material with 1:2 mass ratio of thiourea and sodium alginate showed the highest removal of TC and Cu(II) under the reaction condition of pH= 7. The removal process of both TC and Cu(II) follows the pseudo-second-order adsorption model and Langmuir isotherm model. UA-Ca had a high adsorption capacity toward TC and Cu(II) with the maximum value of 1.099 mmol/g and 2.793 mmol/g based on the Langmuir model at 298 K, respectively. Thermodynamical parameters revealed that TC and Cu(II) adsorption is spontaneous with endothermic nature. Competing ionic cations (Ca 2+ 、Mg 2+ 、NH 4 + ) and organics (sulfamethoxazole, hygromycin) had a certain inhibitory effect on the removal of TC and Cu(II) by UA-Ca, whereas the anionic ions (CO 3 2- 、PO 4 3- 、SO 4 2- ) all had little effect on its removal. Fourier transform infrared spectra and X-ray photoelectron spectroscopy analyses showed that the removal of TC and Cu(II) by UA-Ca was mainly due to electrostatic adsorption and surface complexation. This work provides a promising UA-Ca material for the effective removal of TC and Cu(II) in contaminated water.

研究领域: 环境科学 · 材料科学
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ACS Sustainable Chemistry & Engineering · 2024 · IF 7.1

Easy Preparation, High Water Resistance Glucose-Based Environment-Friendly Wood Adhesives

Qianyu Zhang,Hong Lei,Guanben Du,Antonio Pizzi,Jiaxuan Song,Long Cao,Buapan Puangsin,Xuedong Xi

Recently, formaldehyde-free environment-friendly bio-based wood adhesives have been a hot research topic in the wood industry. Glucose is a widely sourced biomass material, presenting also good reactivity, which has made it a focus of cutting-edge research. In the work presented here, a new formulation was developed for preparing a glucose-based biomass adhesive with excellent bonding strength and water resistance. Glucose was oxidized by sodium periodate at room temperature to generate bioaldehydes (OG), which were then reacted with a polyurea (HU) synthesized by reaction of hexamethylene diamine (HMD) with urea (U) via deamination. This resulted in an environmentally friendly green glucose-based adhesive (OGHU resin) containing neither formaldehyde nor other toxic volatile aldehydes. The effect of the mass ratio of HU/OG on the resin properties was investigated. The results showed that the OGHU resin imparted to the plywood bonded with excellent bonding strength and water resistance. The dry shear strength, 24 h cold water soaking wet strength, 3 h hot water (63 °C) wet strength, and 3 h boiling water wet strength were as high as 1.48 1.16, 1.26, and 1.12 MPa, respectively. Its superior bonding performance exceeded the expectations of the GB/T 9846–2015 standard (≥0.7 MPa) sufficiently to be considered as a substitute for the currently used urea-formaldehyde wood panel adhesives.

CAS / MDL: 124-09-4
研究领域: 材料科学 · 林业工程 · 生物质化学
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CHEMICAL RESEARCH IN TOXICOLOGY · 2024 · IF 3.7

CYP3A4-Mediated Metabolic Activation and Cytotoxicity of Chlortoluron

Xinxin Guo,Mingyu Zhang,Ya Li,Zifang Ding,Minglu Liu,Weiwei Li,Ying Peng,Jiang Zheng

Chlortoluron (CTU) is an herbicide extensively used in agricultural settings for crop cultivation. Its presence in water has been identified as a pollutant detrimental to aquatic species. The objective of the present study was to explore the metabolic activation and hepatotoxicity of CTU. Through human and rat liver microsomal incubations supplemented with CTU, nicotinamide adenine dinucleotide phosphate (NADPH), and either glutathione or N-acetyl cysteine, a benzylic alcohol metabolite (M1) was discerned, alongside a phenol metabolite (M2), a glutathione conjugate (M3), and an N-acetyl cysteine conjugate (M4). In rats exposed to CTU, biliary M3 and urinary M4 were detected in their bile and urine, respectively. The generation of M1 was detected in the presence of NADPH. The observation of M3 and M4 suggests the formation of an iminoquinone methide intermediate arising from the oxidation of M1. CYP3A4 was found to be the principal enzyme catalyzing the metabolic activation of CTU. Furthermore, CTU exhibited cytotoxic properties in cultured rat primary hepatocytes in a concentration-dependent pattern. Concomitant treatment of hepatocytes with ketoconazole mitigated their susceptibility to the cytotoxic effects of CTU.

CAS / MDL: 616-91-1 70-18-8
研究领域: 环境科学 · 毒理学 · 药理学
✓ 已验证 产品关联 DOI PubMed 高影响因子
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CARBOHYDRATE POLYMERS · 2024 · IF 10.7

Preparation and characterization of polymeric cellulose wood adhesive with excellent bonding properties and water resistance

Qianyu Zhang,Ranjun Yan,Yangyang Xiong,Hong Lei,Guanben Du,Antonio Pizzi,Buapan Puangsin,Xuedong Xi

Developing the most abundant cellulose resources in nature as wood adhesives is a challenging but significant work. In this study, an oxidized cellulose-hexamethylene diamine-urea (OCHU) resin adhesive, of high bonding performance, and excellent water resistance has been prepared. The cellulose was firstly enzymatically hydrolyzed to increase its solubility and expose more hydroxyl groups, then oxidized by sodium periodate (NaIO 4 ) to generate a biological compound being rich of aldehyde groups. The OCHU adhesive was prepared by crosslinking oxidized cellulose (OC) with a synthetic reactive polyurea (HU) polymer, which was formed through the deamidation reaction between hexamethylenediamine (H) and urea (U). This adhesive exhibited a 24 h cold water soaking strength of 1.61 MPa, 3 h hot water (63 °C) strength of 1.05 MPa and a dry strength of 1.71 MPa. Compared to oxidized cellulose-hexamethylenediamine (OCH) adhesive, a significant increase of 60 % in this adhesive's wet strength. The Schiff base and addition reactions in the preparation were confirmed by XPS, solid-state NMR, and FTIR. This cellulose-based wood adhesive has great market competitiveness for mass production and application in the plywood industry, due to its excellent bonding properties.

CAS / MDL: 124-09-4
研究领域: 材料科学 · 林业工程
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