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JOURNAL OF POLYMER SCIENCE · 2023 ·Vol. 61 ·期 9 ·842-851 · IF 3.4

A novel bisphenol A-free polyarylates synthesis strategy: 4,4′-sulfobisphenol/2,2-bis(4-hydroxyphenyl)butane co-polyarylate prepared by interfacial polymerization

Zhoufeng Wang,Bolin Wang,Yingying Liu,Junwei Hu

A series of bisphenols, 4,4′-sulfobisphenol (BPS)/2,2-bis(4-hydroxyphenyl)butane (BPB) co-polyarylates with amorphous structures were synthesized from two BPS and BPB, and two different structures of benzoyl chloride monomers. The results of DFT calculations showed that the reaction activation energy of BPB with isophthaloyl chloride (IPC) and terephthaloyl chloride (TPC) was 8.05–8.40 Kcal/mol. The reaction activation energy of BPS with IPC and TPC was 38.73–39.09 Kcal/mol. GPC test results were consistent with theoretical calculations with BPS content from 0% to 15% resulting in a copolymer Mn of 22,000–11,600 and a Mw of 46,100–34,800. The intrinsic viscosity of co-polyarylates ranged from 0.55 to 0.71 dL/g. The glass transition temperature ( T g ) and 5% thermal weight loss of the co-polyarylates were 179.3–205.4 °C and 461.4–487.8 °C, respectively. Improved solubility of co-polyarylates in polar solvents. At the same time, the introduction of BPS did not result in any loss of mechanical properties, with Young's modulus in the range of 1444.32–1870.45 MPa, elongation at break in the range of 23.7%–30.8%, and tensile strength in the range of 52.21–59.38 MPa. Graphical

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JOURNAL OF APPLIED POLYMER SCIENCE · 2023 ·Vol. 140 ·期 19 ·e53836 · IF 3

High antibacterial durability of silver nanoparticles anchored on cotton fiber surfaces by 4-vinylpyridine polymers synthesized via a “grafting through” strategy

Jinlin Chen,Xiaodong Wen,Fang Xu,Shuangfei Xiang,Shujun Zhao,Feiya Fu,Xiangdong Liu,Ni Li

This study aims at developing novel methodology to prepare antibacterial cotton fabric with excellent antibacterial durability, and a “grafting through” approach was adopted to enhance affinity of Ag NPs with cotton fiber surfaces. The surface modification was carried out by covalently linking acrylic acid (AA) molecules onto the fibers, then 4-vinylpyridine was copolymerized with the AA moieties as a polymeric binder. Once the coordination bonds were formed between silver nanoparticles (Ag NPs) and the pyridine nitrogen, Ag NPs could be stably immobilized on the cotton fabric. Experimental results showed that the AA-co-PVP grafting copolymer had a significant regulatory effect on the dispersion and particle size of Ag particles, and the resulting cotton fabric presented a high antibacterial property with excellent durability. Even after 120 washing cycles, the bacterial reduction rates of the modified fabric against both Staphylococcus aureus and Escherichia coli retained a level higher than 99%. In addition, other textile attributes, such as vapor transmissibility, water absorbability and flexibility, could be largely retained in the modified fabrics.

CAS / MDL: 64-19-7
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JOURNAL OF SOLID STATE CHEMISTRY · 2023 · IF 3.3

Controllable synthesis of sea urchin-like Cu–Au bimetallic nanospheres and their utility as efficient catalyst for hydrogenation of 4-nitrophenol

Yawen Guan,Shanshan Fu,Wanyu Song,Xueyan Zhang,Bangyu Liu,Fang Zhang,Fang Chai

4-nitrophenol (4-NP) is a harmful aromatic compound to environment. The catalytic hydrogenation of 4-NP was considered as a profitable approach due to the valuable organic intermediate product. High efficiency catalysts are crucial. Herein, Cu–Au bimetallic nanospheres (BNSs) with sea urchin structure were fabricated by tuning the reaction condition and ratio of precursors. The Cu–Au BNSs exhibited effective catalytic activity in the reduction of 4-NP and K 3 [Fe(CN) 6 ]. The optimum catalyst can be determined as the Cu–Au BNSs prepared by 15 ​mL AA, 4-NP can be reduced to 4-AP in 150 ​s ​(k ​= ​3.02 ​× ​10 −2 s −1 ) with TOF value of 0.149 (s −1 ). The reusability of Cu–Au BNSs was evaluated with high effectiveness, the catalytic activity remained negligible loss over 18 cycles with efficiency over 95%, indicated their good reusability, which can be attributed to the synergistic effect of Cu–Au BNSs. The fabrication of bimetallic nanostructures provided an efficient approach to design efficient catalyst.

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Materials Today Energy · 2023 · IF 9.3

4-tert-butylpyridine induced Ni3+/Ni2+ ratio modulation in NiOx hole transport layer towards efficient and stable inverted perovskite solar cells

Taotao Hu,Hongming Hou,Jin Peng,Qiaofeng Wu,Jialong He,Hua Yu,Rui Liu,Tian Hou,Xiangqing Zhou,Meng Zhang,Xiaolong Zhang,Xinchun Yang,Yuanmiao Sun,Xuanhua Li,Yang Bai

NiO x plays a vital role in fabricating efficient and stable inverted perovskite solar cells (PSCs). However, the relatively low conductivity and inefficient hole extraction of NiO x hole transport layer (HTL) due to the low Ni 3+ /Ni 2+ ratio limit its use in high-efficiency PSCs. Here, we report a facile strategy to remarkably enhance the electrical conductivity and hole extraction capability of NiO x HTL by simply introducing the small molecule 4- tert -butylpyridine ( t BP) as additive in the NiO x precursor solution. It is revealed that the t BP efficient improves the charge selectivity of the NiO x interface, inducing the preferable p-type carrier concentration on the surface. Consequently, more oxygen is involved in the process of Ni 2+ to Ni 3+ conversion, and the resulting t BP: NiO x HTL exhibits significantly enhanced hole extraction and transport property. In addition, a thin layer of LiF is applied to passivate the surface of NiO x , which enables improved hole migration ability by the dipole effect of LiF and reduced trap state density of the surface. The inverted PSCs (0.16 cm 2 ) fabricated with t BP: NiO x HTL delivers an enhanced efficiency of 20.2% relative to the control devices (17.5%). t BP: NiO x devices with a large area of 1 cm 2 are also demonstrated, which achieve a decent efficiency of 16% with excellent long-term stability.

CAS / MDL: 64-17-5 141-43-5 67-63-0
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ACS Applied Materials & Interfaces · 2018 · IF 8.097

Fabrication of a High-Quality Cu2ZnSn(S,Se)4 Absorber Layer via an Aqueous Solution Process and Application in Solar Cells

Wangen Zhao,Fengyang Yu,Shengzhong Frank Liu

The development of Cu2ZnSn(S,Se)4 (CZTSSe) solar cells determines the prospect of thin-film photovoltaic devices because of some of their strengths. However, the usual solution fabrication processes of CZTSSe absorbing layers are either too tedious or highly toxic. Here, we have developed an alternative strategy to prepare kesterite CZTSSe absorber films with a simple and low-toxicity solution process by replacing the commonly employed thiol-based compounds using the glycolic acid aqueous solution, which significantly reduces the environment pollution and toxicity, providing a possibility toward the green solvent process. The power conversion efficiency of 6.81% has been acquired based the aqueous solution-processed CZTSSe thin film via optimizing the fabrication technology.

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CHEMICAL ENGINEERING JOURNAL · 2019 · IF 8.355

Cellulosic protic ionic liquids hydrogel: A green and efficient catalyst carrier for Pd nanoparticles in reduction of 4-nitrophenol in water

Xiang Li,Fuping Dong,Lihua Zhang,Qinqin Xu,Xianyi Zhu,Songmiao Liang,Lijie Hu,Haibo Xie

The design and fabrication of functional hydrogel materials for environmental catalysis is a frontier topic both in fields of material science and catalysis. In this study, a new cellulosic hydrogel anchoring 1,1,3,3-tetramethyl guanidinium–based ionic liquids moiety (CHI) was firstly prepared by simply adding bicyclic anhydrides into newly developed 1,1,3,3-tetramethyl guanidine/DMSO/CO 2 solvent system for cellulose. The presence and amount of bicyclic anhydrides as a cross linker was proved to be an important factor for the hydrogel formation. And then, Pd nanoparticles (NPs)@CHI composites were fabricated by the reduction of the absorbed Pd(II) ions on CHI using NaBH 4 as reducing agent. The samples were characterized by techniques of 1 H NMR, 13 C NMR, FT-IR, SEM, TEM, EDX, XPS, XRD and ICP-OES analysis. It was identified that the CHI presented good immobilization capacity of Pd NPs, and the achieved Pd NPs@CHI composite had high catalytic activity and excellent reusability for the reduction of 4-nitrophenol in water. The activation parameters of the reduction reaction of 4-nitrophenol catalyzed by Pd NPs@CHI using NaBH 4 were calculated as Ea = 10.8 kJ mol −1 , ΔH #  = 8.1 kJ mol −1 and ΔS #  = −234.8 J mol −1  K −1 .

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SENSORS AND ACTUATORS B-CHEMICAL · 2019 · IF 6.393

4-Mercaptophenylboronic acid modified Au nanosheets-built hollow sub-microcubes for active capture and ultrasensitive SERS-based detection of hexachlorocyclohexane pesticides

Xia Zhou,Qian Zhao,Guangqiang Liu,Weiping Cai

Active capture and ultrasensitive SERS-based detection of hexachlorocyclohexane (HCH) has been a challenging task. A novel strategy based on 4-mercaptophenylboronic acid (4-MPBA) surface modification on Au nanosheets-built hollow sub-microcubes (ANHCs) was proposed to capture HCH pesticides effectively via Suzuki cross coupling reaction. The ANHCs structure composed of numerous intertwined nanosheets was firstly prepared by Au nanocrystals heteroepitaxial growth on AgCl cubes. Then, the 4-MPBA molecules were selected to modify on the surface of ANHCs for SERS-based detection of HCH. The SERS results proved that active capture and ultrasensitive detection of HCH could be implemented, and the limit of detection is 0.3 ppb. Besides, 4-MPBA modified substrate show high reproducibility and sensitivity than unmodified one. Moreover, the characteristic peak intensity ratio I HCH /I 4-MPBA presents a good linear relationship with the logarithm of a certain concentrations, and achieve SERS-based quantitative detection of HCH. In addition, this strategy has been successfully used for the detection and differentiation of mixed HCH isomers in water samples. The surface modification strategy on high performance SERS substrate provides a good route for the highly ultrasensitive detection and active capture of HCH, and paves a way for the detection of organochlorine pesticide residues in water samples.

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ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY · 2018 · IF 3.974

Synergistic effect of co-exposure to cadmium (II) and 4-n-nonylphenol on growth inhibition and oxidative stress of Chlorella sorokiniana

Lu Wang,Yuan Kang,Siyun Liang,Danying Chen,Qiuyun Zhang,Lixuan Zeng,Jiwen Luo,Feng Jiang

Toxicological effect of freshwater algae co-exposure to Cd and 4-n-nonylphenol (4-n-NP) was seldom reported. In the present study, Chlorella sorokiniana was selected for testing the single and combined effect of Cd and 4-n-NP by detecting the growth inhibition and oxidative stress after exposure for 48 h, 72 h, and 96 h. The combined effects were evaluated by using toxic units (TU) method and concentration addition(CA)model. The synergistic effect of mixture on algal growth inhibition was both observed at 48 h and 72 h, and the additive effect was observed at 96 h. In addition, the significant alterations of superoxide, thiobarbituric acid reactive substances and antioxidant defenses (superoxide dismutase, catalase , glutathione) have been detected. It could be observed that the mixture predominantly lead to synergistic effects in superoxide induction, and the antagonistic effects in the GSH induction. A similar trend between the superoxide induction and growth inhibition were observed, which may indicate that the oxidative effects of Chlorella sorokiniana contributed to the growth inhibition after exposure to Cd and 4-n-NP. These findings may have important implications in the risk assessments of heavy metals and endocrine disruptors in the aquatic environment.

CAS / MDL: 7440-43-9
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JOURNAL OF HAZARDOUS MATERIALS · 2018 · IF 6.434

pH-mediated reversible fluorescence nanoswitch based on inner filter effect induced fluorescence quenching for selective and visual detection of 4-nitrophenol

Lei Han,Shi Gang Liu,Jia Yu Liang,Yan Jun Ju,Nian Bing Li,Hong Qun Luo

Being a common hazardous waste, 4-nitrophenol (4-NP) has caused a serious threat to humans and environment. Therefore, rapid and selective detection of 4-NP, especially using a simple and portable instrument, is highly desired for human health and environmental monitoring. Herein, we develop a novel pH-mediated reversible fluorescence nanoswitch for selectively detecting 4-NP by using water-soluble fluorescent polymer carbon dots (PCDs) as a probe. The fluorescence of PCDs can be quenched by 4-NP via inner filter effect (IFE) because its excitation spectrum well overlaps with the absorption spectrum of 4-NP under alkaline condition. However, an obvious blue shift of the absorption peak of 4-NP occurs under acidic condition, causing the fluorescence recovery of PCDs due to the disappearance of IFE. On the basis of this principle, a pH-mediated reversible fluorescence nanoswitch was constructed and a broad linear range was obtained from 0.5 to 60 μM with a detection limit of 0.26 μM for 4-NP. Furthermore, this approach was successfully applied to detect 4-NP in real water samples and a portable polyamide film-based sensor was developed for visual detection of 4-NP, which offers a promising platform for the detection of 4-NP in on-site and resource-poor settings.

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JOURNAL OF CHEMICAL AND ENGINEERING DATA · 2018 · IF 2.196

Measurement and Thermodynamic Models for Ternary Liquid–Liquid Equilibrium Systems {Water + Polyoxymethylene Dimethyl Ethers +4-Methyl-2-pentanol} at Different Temperatures

Liping Wang,Saisai Zhou,Pan Li,Pengzhou Li,Qingsong Li,Yingmin Yu

Polyoxymethylene dimethyl ethers (DMMn) have attracted particular attention in industry as excellent oxygenated fuel additives. This study aims to reveal the liquid–liquid equilibrium (LLE) values regarding ternary mixtures {water + methylal (DMM1) + 4-methyl-2-pentanol (MIBC)}, {water + DMM2 + MIBC}, {water + DMM3 + MIBC}, and {water + DMM4 + MIBC} at 298.2 and 308.2 K under 101.3 kPa. Distribution factor and selectivity were utilized to assess the extracting capabilities of the selected extractant. The well known Hand equation and Othmer–Tobias equation were utilized to test the consistency of the LLE values. In addition, the experimental results were correlated by the UNIQUAC and NRTL thermodynamic models with all of the root-mean-square deviation values less than 0.0127,which indicated that both models agree well with the experimental tie-line data.

CAS / MDL: 109-87-5 108-11-2
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JOURNAL OF CHEMICAL AND ENGINEERING DATA · 2018 · IF 2.196

Solid–Liquid Phase Equilibria of the Ternary System (2-Naphthaldehyde + 4-Methylphthalic Anhydride + Ethyl Acetate) at (288.15, 298.15, and 308.15) K

Xiaoqiang Gao,Fang Zhang,Yi Yu,Yonghui Dou,Li Xu,Guoji Liu

The solubility of 2-naphthaldehyde (2-NA) and 4-methylphthalic anhydride (4-MA) in ethyl acetate at temperatures from 283.15 to 313.15 K and solid–liquid equilibrium of ternary (2-NA + 4-MA + ethyl acetate) system at temperatures of (288.15, 298.15, and 308.15) K were measured under pressure of 101.3 kPa. Three isothermal phase diagrams were plotted according to the ternary solubility data. For the ternary system, two pure 2-NA and 4-MA solids were formed at each temperature and determined by the wet residue method of Schreinemaker. The crystalline region of 2-NA decreases with the increase in temperature, and 4-MA is just the opposite. The crystallization region of 2-NA was found to be smaller than that of 4-MA. The solubility data of the system were correlated and calculated by NRTL and Wilson models. The results show that the NRTL model agrees well with the experimental data compared with the Wilson model. Furthermore, the densities of equilibrium solutions were determined at the corresponding temperatures.

CAS / MDL: 7631-99-4
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Journal of CO2 Utilization · 2018 · IF 5.503

Selective hydrodeoxygenation of lignin β-O-4 model compounds and aromatic ketones promoted by palladium chloride with acidic CO2/MeOH system

Yu Cao,Ran Ma,Ning Wang,Mei-Yan Wang,Xue-Dong Li,Liang-Nian He

Selective hydrogenolysis is a crucial challenge for lignin valorization. A PdCl 2 -catalyzed hydrogenolysis of C OH bond of various lignin β-O-4 alcohol model compounds was developed for preparation of corresponding phenethoxybenzene in 78–98% isolated yield. Notably, the introduction of low-pressure CO 2 (1 MPa) remarkably improves the reaction efficiency and selectivity of phenethoxybenzene. Neither over-reduction of aromatic ring nor further debenzylation was detected. This is understandable that the in situ methylcarbonic acid generated from CO 2 and methanol acts as an acidic catalyst and enhances the leaving ability of hydroxyl group of β-O-4 alcohols. Besides, the present PdCl 2 /CO 2 /MeOH catalyst system proved to be effective for reductive cleavage of C O bonds of β-O-4 ketones, producing ethylbenzenes accompanied with phenols in high yields. Furthermore, this protocol could also be extended to selective hydrodeoxygenation of the carbonyl group to methylene in aromatic ketones. As a sound reaction medium, such in situ CO 2 /MeOH acidic system could be inherently neutralized by depressurizing CO 2 , providing feature advantages for simple post-processing and none waste disposal.

CAS / MDL: 98-86-2
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