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Surfaces and Interfaces · 2025 · IF 6.3

Eco-friendly and highly efficient rust removal for Q235 steel via UV-induced copolymerization of acrylic monomers into adsorptive gel

Jianyang Liu,Wei Wang,Zhipeng Mao,Lin Cao,Meiyan Yu,Shougang Chen

Metal corrosion and rusting have caused significant losses to humans, and environmentally friendly and efficient rust removal methods are receiving increasing attention. Here, we propose a method for rust removal by synthesizing acrylic gel on Q235 steel sheet using a photopolymerization reaction. The weak acidity of acrylic acid decomposes rust, and the gel formed by the reaction of acrylic acid with acrylamide has strong adsorption capacity, which effectively adsorbs rust molecules and metal ions. The introduced Cu 2 O enhances the rust removal system. Cu 2 O reacts with the acrylic acid monomer to form a monovalent copper complex, which can improve the rust removal efficiency during the process through redox reactions. The UV-induced copolymerization of acrylic monomers to form gel enables effective rust removal, with a rust removal rate as high as 85.94 g ·h –1 ·m –2 . This method avoids the use of strong acids commonly found in traditional rust removal methods, offering advantages such as environmental friendliness and low cost. The gel formed during the rust removal process can be easily and conveniently removed from the substrate surface, thus avoiding secondary pollution issues such as waste liquid disposal.

CAS / MDL: 110-26-9 79-06-1 79-10-7
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JOURNAL OF HAZARDOUS MATERIALS · 2025 · IF 11.3

In Vitro metabolism of six representative organic UV stabilizers (OUVs) in marine fish liver microsomes: Kinetics, mechanisms and bioaccumulation evaluation

Yuchen Wang,Qianyi Huang,Siqi Zhang,Shan Liu,Hengxiang Li,Xiaodong Wang,Yan Wang,Rui Hou,Xiangrong Xu

The ubiquitous occurrence of organic UV stabilizers (OUVs) poses a potential threat to marine fish, but the metabolism of OUVs in the body remains a missing piece of the puzzle in their ecotoxicology. This study investigated the in vitro metabolism of six OUVs in the liver microsomes of an economically valuable marine fish ( Lateolabrax japonicus ). The depletion of the six OUVs follows first-order kinetics in the microsomes, with in vitro depletion rate constants ( k depl ) ranging from 0.23 to 0.40/h. The intrinsic clearance ( CL int ) of 1H-benzotriazole (BT) was estimated to be 0.0026  μ L/(min·mg·protein). The enzyme inhibition experiments and molecular docking results highlight the importance of cytochrome P450 enzyme (CYP) 3A4 in OUVs metabolism. Among the 4 metabolizable compounds, some metabolites from hydroxylation, methylation, acetylation and conjugation were tentatively identified. In addition, the in vitro transformation rates can more accurately predict the whole-body bioconcentration potential via an in vitro to in vivo extrapolation (IVIVE) model.

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COMPOSITES COMMUNICATIONS · 2025 · IF 7.7

Flame-retardant and UV-resistant polycarbonate composites with well-preserved mechanical properties enabled by silsesquioxane/sulfonate-functionalized nano carbon black

Xiaodi Ye,Cheng Zhan,Ting Sai,Bingtao Wang,Juan Li,Chengfeng Zhang,Yanfei Wang,Zhenghong Guo,Siqi Huo

A sulfonate/silsesquioxane-functionalized nano carbon black (CBSP) was synthesized by grafting polyhedral oligomeric silsesquioxane (POSS) and sulfonate groups onto carbon black (CB) surface, aiming to meet practical requirements of outdoor-used polycarbonate (PC). Upon adding 1 wt% CBSP, PC/1.0CBSP composite displayed a limiting oxygen index (LOI) of 31.3 % with a vertical burning (UL-94) V-0 classification. Its peak heat release rate (PHRR) and total smoke release (TSR) were decreased by 39 % and 21 % relative to PC. The superior fire retardancy can be attributed to the triple reinforced effect from CB, sulfonates and POSS by promoting the formation of denser and more resilient char layers. CBSP well preserved mechanical performances of PC due to its reinforced interfacial compatibility and improved UV shielding through the absorption of UV photons by CB. This work provides a feasible strategy for fabricating fire-retardant PC composites with superior mechanical robustness and UV-resistant properties, expecting to increase applicability and lifespan.

CAS / MDL: 515-74-2
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ACS Sustainable Chemistry & Engineering · 2018 · IF 6.14

UV-Cured Fluoride-Free Polyurethane Functionalized Textile with pH-Induced Switchable Superhydrophobicity and Underwater Superoleophobicity for Controllable Oil/Water Separation

Kunlin Chen,Weiwei Gou,Xuemei Wang,Chanjuan Zeng,Fangqing Ge,Zhenjiang Dong,Chaoxia Wang

Design and fabrication of smart surfaces for separation of oily water have been developed rapidly. Nevertheless, construction of these smart surface materials by using green and sustainable paths for intelligent separation of oily water still faces huge challenges. The aim of this study was to develop a facile, sustainable, and energy-efficient approach for the fabrication of smart coatings with pH-responsive switchable wettability. The coating was formed on the textiles from UV-cured fluoride-free pH-responsive polyurethane (pH-PU). The wettability of obtained textiles could switch reversibly between superhydrophobicity and underwater superoleophobicity due to the protonation and deprotonation of the pH-PU under different pH conditions, which was used to successfully separate either oil or water from oily water with high separation efficiencies. More importantly, oil-in-water and water-in-oil emulsions could all be selectively separated with high water flux and oil purity by as-fabricated textiles, and these pH-PU-functionalized textiles or sponges effectively performed for oil collection of oil spilled on water. Our work provided a fast, economical, and sustainable pathway to prepare smart coatings with switchable wettability for both environmental protection and energy-saving merits.

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CHEMOSPHERE · 2017 · IF 4.208

Degradation of diethyl phthalate (DEP) by UV/persulfate: An experiment and simulation study of contributions by hydroxyl and sulfate radicals

Ziying Wang,Yisheng Shao,Naiyun Gao,Xian Lu,Na An

Degradation of diethyl phthalate (DEP) by ultraviolet/persulfate (UV/PS) process at different reaction conditions was evaluated. DEP can be degraded effectively via this process. Both tert-butyl (TBA) and methanol (MeOH) inhibited the degradation of DEP with MeOH having a stronger impact than TBA, suggesting sulfate radical ( ) and hydroxyl radical (HO ) both existed in the reaction systems studied. The second-order rate constants of DEP reacting with and HO were calculated to be ( 6.4 ± 0.3 ) × 10 7 (6.4±0.3)×107 M −1 s −1 and ( 3.7 ± 0.1 ) × 10 9 (3.7±0.1)×109 M −1 s −1 , respectively. To further access the potential degradation mechanism in this system, the pseudo-first-order rate constants (k o ) and the radical contributions were modeled using a simple steady-state kinetic model involving and HO . Generally, HO had a greater contribution to DEP degradation than . The k o of DEP increased as PS dosages increased when PS dosages were below 1.9 mM. However, it decreased with increasing initial DEP concentrations, which might be due to the radical scavenging effect of DEP. The k o values in acidic conditions were higher than those in alkaline solutions, which was probably caused by the increasing concentration of hydrogen phosphate (with higher scavenging effects than dihydrogen phosphate) from the phosphate buffer as pH values rose. Natural organic matter and bicarbonate dramatically suppressed the degradation of DEP by scavenging and HO . Additionally, the presence of chloride ion (Cl − ) promoted the degradation of DEP at low Cl − concentrations (0.25–1 mM). Finally, the proposed degradation pathways were illustrated.

✓ 已验证 DOI 高影响因子
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Heliyon · 2023 · IF 4

Development and validation of a novel HPLC-UV method for simultaneous determination of azathioprine metabolites in human red blood cells

Hengyi Yu,Dongyan Li,Dong Xiang,Xiping Li,Lu Liu,Dong Liu,Xuepeng Gong

A rapid, specific and accurate high-performance liquid chromatography with tunable ultraviolet detection method was developed to simultaneously determine azathioprine metabolites, 6-thioguanine nucleotides (6-TGN) and 6-methyl mercaptopurine riboside (6-MMPr) in human red blood cells. Erythrocyte lysate sample was precipitated by perchloric acid under the protection of dithiothreitol, with 6-TGN and 6-MMPr being acid hydrolyzed to produce 6-thioguanine (6-TG) and 6-methymercaptopurine (6-MMP). A Waters Cortecs C 18 column (2.1 × 150 mm, 2.7 μm) was used for chromatographic separation with a water (containing 0.01 mol/L ammonium acetate and 0.2% acetic acid)/methanol linear gradient at a flow rate of 0.45 mL/min in a 5.5 min. UV detection wavelengths were 340 nm for 6-TG, 303 nm for 6-MMP and the IS (5-bromouracil). The calibration curves fitted a least squares model (weighed 1/ x 2 ) from 0.15 to 15 μmol/L for 6-TG ( r 2  = 0.9999) and from 1 to 100 μmol/L for 6-MMP ( r 2  = 0.9998). This method was validated according to the FDA bioanalytical method validation guidance and ICH M10 bioanalytical method validation and study sample analysis guidance for industry, and successfully utilized in ten IBD patients receiving azathioprine therapy.

✓ 已验证 DOI PubMed 高影响因子
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2021 · IF 4.539

Non-metal group doped g-C3N4 combining with BiF3:Yb3+, Er3+ upconversion nanoparticles for photocatalysis in UV–Vis–NIR region

Chunyan Zhang,Zhendong Fu,Feng Hong,Ge Pang,Tengri Dong,Yunxiao Zhang,Guixia Liu,Xiangting Dong,Jinxian Wang

Broad spectrum response photocatalyst is crucial for making full use of sunlight and widely used in efficient photocatalytic degradation of organic dyes. In this work, upconversion luminescence boosted broadband photocatalysts based on BiF 3 :Yb 3+ , Er 3+ nanoparticles (BFY) and the carbon nitride doped with various masses of barbituric acid (CNB x ) semiconductor materials (BFY/CNB x ) were successfully designed and produced for photocatalysis in UV–Vis–NIR region. Compared with pure g-C 3 N 4 , BFY/CNB 0.5 composites have better photocatalytic performance attributed to the utilization of broadband spectrum energy and effective charge separation. After 30 min illumination by visible light , photodegradation efficiency of RhB reaches about 99.4% by using BFY-2/CNB 0.5 . A plot of C/C 0 versus time indicates that the BFY-2/CNB 0.5 can degrade about 64.7% of RhB in 80 min by NIR irradiation. Under simulated solar light, the sample of BFY-2/CNB 0.5 reaches a maximum degradation efficiency of 98.0% within 15 min. The strengthened photocatalytic activity is due to the synergistic effect of CNB 0.5 and upconversion materials. The active species utilized in the degradation process were examined using capture experiments. After four continuous photocatalytic cycles, about 94.0% of RhB solution is degraded. The photocatalytic mechanism of the composite photocatalysts is also analyzed in detail. The results indicate that the prepared BFY/CNB 0.5 photocatalysts have good prospects in the field of environmental remediation.

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JOURNAL OF THERMOPLASTIC COMPOSITE MATERIALS · 2024 · IF 3.6

Application of titanium dioxide nanorod (TNr)@SiO2 with low photocatalytic effect and high UV resistance in poly(vinyl chloride) film

Jianhao Cheng,Chen Shi,Yubing Dong,Jian Han

Ultraviolet (UV) radiation has a detrimental effect on the outdoor lifetime of PVC film materials. TiO2 nanoparticles, as commonly used UV absorbers, still suffer from poor transparency, high photocatalytic effect, and poor dispersion in PVC matrix. To mitigate these effects effectively, titanium dioxide nanorod @ silicon dioxide (TNr@SiO2) was synthesized and used as an anti-UV aging agent for polyvinyl chloride (PVC). The agglomeration effects of TiO2 nanoparticles in PVC films were solved by synthesizing TNr, and the catalytic effects of TiO2 was reduced by growing SiO2 on the TNr surface. Scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and UV-visible spectroscopy were utilized to demonstrate the excellent dispersion and low photocatalytic effects of the synthesized TNr@SiO2. Compared with pure PVC film, the color change of TNr@SiO2/PVC composite film is not evident after 800h of UV aging, and the retention of mechanical properties were 93.94%. Compared with TiO2/PVC, TNr@SiO2/PVC composite film has better transparency. Results show that TNr@SiO2 can maintain the properties of PVC better because the electrons of TNr@SiO2 are excited to form a positively charged hole after the absorption of UV light, and then the hole electron pairs are recombined and converted into thermal energy, which improves the durability of PVC. Therefore, this highly transparent TNr@SiO2/PVC composite film with low photocatalytic activity and high UV resistance will soon be applied in large-scale industrial production.

✓ 已验证 DOI 高影响因子
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Journal of Cleaner Production · 2022 · IF 11.072

Interface nanoengineering of a core-shell structured biobased fire retardant for fire-retarding polylactide with enhanced toughness and UV protection

Yueming Yu,Yan Zhang,Liangdong Xi,Zhinuo Zhao,Siqi Huo,Guobo Huang,Zhengping Fang,Pingan Song

In this work, we found a very effective method to adjust the polarity of the fillers to promote its good dispersion in matrix by using an organic-solvent-free assembling strategy. With the coating of polyethylenimine-decorated graphene oxide (GO-PEI), the as-prepared biobased core-shell graphene oxide hybrid (BCSGOH) can distribute more homogeneously in the polylactide (PLA) matrix, compared with the bio-derived core-shell flame retardant (CSFR) with higher polarity. The polarity analysis of BCSGOH, CSFR and PLA indicated that the polarity of BCSGOH had a better match with that of PLA, and the interfacial tension (0.8 mN/m) between BCSGOH and PLA was much lower than that (12.0 mN/m) between CSFR and PLA. Consequently, the better flame retardancy, impact toughness and UV-shielding properties of PLA/BCSGOH composites were achieved. 6 wt% of BCSGOH endowed PLA with the best comprehensive properties, such as the UL94 V-0 rating, the limiting oxygen index (LOI) of 30.0%, and notched impact strength of 12.38 kJ/m 2 . Hence, this work offers a conducive, facile and green strategy to create high-performance fire-safe bioplastics .

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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Disinfection and mechanism of super-resistant Acinetobacter sp. and the plasmid-encoded antibiotic resistance gene blaNDM-1 by UV/peroxymonosulfate

Shijie Yao,Yaru Hu,Jianfeng Ye,Jianhao Xie,Xuetao Zhao,Lingli Liu,Shuguang Lyu,Kuangfei Lin,Changzheng Cui

The super-resistant bacteria that produce the New Delhi metallo-β-lactamase 1 (NDM-1) enzyme are becoming a conceivably major worldwide clinical issue with serious consequences. Studying the disinfection and mechanism of super-resistant bacteria and their antibiotic resistance genes (ARGs) is crucial for controlling their spread in the water environment. In this study, the disinfection of the super-resistant bacterium Acinetobacter sp. CS-2 and its transferable ARGs (plasmid-encoded bla NDM-1 and bla OXA-58 ) by ultraviolet radiation (UV), peroxymonosulfate (PMS), and ultraviolet/peroxymonosulfate (UV/PMS) exposure were investigated. UV/PMS could completely inactivate CS-2 and control the photoreactivation risk, while bacteria that underwent UV and PMS treatment had survival ratios of 0.22% and 0.28%, respectively. The removal efficiencies of bla NDM-1 and bla OXA-58 ranged from 3.64 to 4.05 log, and the advantage of UV/PMS treatment on ARGs damage was further identified by gel electrophoresis analysis. The removal efficiency of bla NDM-1 was lower than that of bla OXA-58 , which was attributed to the low number of adjacent 5′-TT-3′ harbored by bla NDM-1 . The removal rate constants of the ARGs by UV treatment were significantly correlated with the number of adjacent base pairs (e.g., 5′-TT-3′, 5′-CT-3′, 5′-TC-3′ and 5′-CC-3′) and length, with R -values ranging from 0.9044 to 0.9512. Singlet oxygen ( 1 O 2 ) played a vital role in the reduction of bla NDM-1 and bla OXA-58 in the UV/PMS treatment. UV/PMS showed high removal efficiency under natural pH conditions and in the presence of various aqueous ions (e.g., Cl − , SO 4 2− and HCO 3 − ). Overall, this study provides new understandings and theoretical support for the risk control of super-resistant bacteria and plasmid-encoded ARGs.

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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2020 · IF 4.939

Down-conversion Ce-doped TiO2 nanorod arrays and commercial available carbon based perovskite solar cells: Improved performance and UV photostability

Koucheng Chen,Heng Zhang,Hui Tong,Ling Wang,Lu Tao,Ke Wang,Yinxi Zhang,Xingfu Zhou

Ce-doped TiO 2 nanorod arrays as the mesoporous supporting layer and TiO 2 compacted electron blocking layer was simultaneously fabricated by one-pot hydrothermal method . Ce-doped TiO 2 nanorod was utilized as down-conversion luminescence centers and commercial available carbon was used in hole-transport-free perovskite solar cells . SEM indicated that the doping of Ce reduced the diameter of TiO 2 nanorods. XRD and EDS spectra demonstrate the successful incorporation of Ce ions. UV–Vis absorption spectra and PL emission spectra show that the down-conversion center Ce 4+ can effectively utilize ultraviolet light and extend the absorption into the ultraviolet region. The carbon-based device using the optimized Ce doping concentration achieved power conversion efficiency (PCE) of 10.1%, which was 24.6% higher than that of undoped device. Ce doping changes the band gap of TiO 2 and the Fermi energy level, and thus improve the open circuit voltage. The open circuit voltage decay curve show that Ce-doped TiO 2 prolongs electron lifetime . EIS analysis hints that more carriers are generated. The UV stability has also been significantly improved., PCE of the optimized Ce-doped device still retains 90% of the initial value , however, the undoped device decreases to 55% of the initial value under light irradiation at ambient atmosphere for 12 h.

✓ 已验证 DOI 高影响因子
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Journal of Environmental Chemical Engineering · 2024 · IF 7.4

UV-crosslinked SBS block copolymers via thiol-ene reaction for efficient absorption and removal of oil/organic solvents from water

Deshun Huang,Guozong Yue,Jing Zhu,Feiyi Liao,Yihong Zhao,Luming Yang

With the urgent need for oil/organic solvents spills disposal, the development of new sorbents with low cost, high sorption capacity, good selectivity and reusability is required. In the current work, three-dimensional structured absorbents have been rapidly fabricated by ultraviolet (UV)-crosslinking of styrene- block -butadiene- block -styrene (SBS) copolymers via thiol-ene reaction in 60 s, using poly-(mercaptopropyl)methylsiloxane (SMS) as crosslinker. The SBS-SMS absorbents were characterized by FT-IR, SEM, XRD, tensile strength, thermogravimetric, gel fraction and water contact angle analysis, which showed high tensile strength, good thermal stability, hydrophobicity, and acceptable gel content. The absorption capacity investigations were carried out in 7 types of organic liquids and 2 types of oils. The SBS-SMS 0.005 exhibited the highest absorption performance in different organics, with the capacities of 74.6 g/g for dichloromethane, 20.1 g/g for kerosene, and 12.8 g/g for diesel oil, respectively. The impacts of sheet thickness on the absorption and desorption kinetics were studied, and the results showed that thinner absorbents illustrated faster absorption and desorption speed. Additionally, the SBS-SMS absorbents showed good selectivity and effectiveness in organic solvents/oil separation from water (separation efficiency > 93 %), well oil retention ability and oil desorption efficiency, floating properties, easy collection, as well as good reusability upon ten absorption-desorption cycles. The current SBS-SMS absorbents should have great potential in practical application for efficient oil/water separation as well as radioactive organic waste liquid treatment.

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