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Water · 2022 ·Vol. 14 ·期 7 ·1007 · IF 3.53

Degradation of 2-Naphthol in Aqueous Solution by Electro-Fenton System with Cu-Supported Stainless Steel Electrode

Xudong Cheng,Xiaoping Zhang,Shaoqi Zhou,Lin Shi

For the treatment of 2-naphthol wastewater, the homogeneous electro-Fenton process was considered as an effective method but some disadvantages greatly restrict its application. The three-dimensional electro-Fenton (3D-EF) system using a nano zero-valent iron-supported biochar (NZVIs-BC) particle electrode and a Cu-supported stainless steel electrode (Cu-SSE) was proposed to avoid the disadvantages of the homogeneous electro-Fenton. In this work, the 3D-EF system was developed, which consisted of a Cu-SSE (cathode), a graphite rod (anode) and a NZVIs-BC particle electrode. The effect of the ratio of ferrous sulfate heptahydrate (FS) to rice straw (RS), CuSO4•5H2O amount, initial pH of 2-naphthol wastewater and current intensity (the output current of the power supply) on the removal rate of 2-naphthol were investigated. It is noteworthy that more than 98.36% of the 2-naphthol in aqueous solution was removed by the 3D-EF system, and only about 60.09% of 2-naphthol was removed by the homogeneous electro-Fenton system. Furthermore, naphthalene, benzoic acid, β-naphthoquinone, 1, 2-naphthalenedione, phenol and aromatic hydrocarbon were the main degradation products of 2-naphthol by the 3D-EF system; the toxicity of 2-naphthol wastewater was also greatly reduced.Keywords:electro-Fenton;Cu-supported stainless steel electrode;nano zero-valent iron-supported biochar;2-naphthol wastewater

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JOURNAL OF LUMINESCENCE · 2022 · IF 4.171

Preparation, structure and optical properties of mixed stacked cocrystals of 2,2':6′,2″-Terpyridine and 1,2,4,5-tetracyanobenzene

Qian Zhou,Yuan Yu,Huitian Du,Chenghao Liu,Junfeng Ren,Shenghao Han,Zhiyong Pang

Organic charge-transfer cocrystals exhibit fantastic physical properties owning to their multi-component synergistic and collective effect. In spite of the abundant material supplies, the cocrystals people prepared so far are far less than expectation. Here, we reported the preparation, structure and optical properties of a mixed stacked cocrystal of 2,2':6′,2″-terpyridine and 1,2,4,5-tetracyanobenzene. The structural and optical properties were analyzed by using single-crystal X-ray diffraction (SCXRD), FTIR, Raman, optical absorption and emission spectra experimentally and the molecular electrostatic potential (MEP), Hirshfeld surface , the reduced density gradient (RDG), frontier molecular orbitals (FMO) theory, inter-fragment charge transfer (IFCT) analysis and time dependent density functional theory (TD-DFT) theoretically. The TTC sample exhibits strong up-conversion luminescence that is absent in their individual components. Theoretical analysis indicates that the NLO properties of TTC may be due to a significant increase in two-photon transition probabilities δ TPA related to intermolecular charge transfer (CT) interactions. Our results may be helpful for a better understanding of NLO mechanism in ground state CT cocrystals.

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SEPARATION SCIENCE AND TECHNOLOGY · 2022 · IF 2.799

Novel multi-hydroxyl containing organo-vermiculite for effective removal of 2-Naphthol: adsorption studies and model calculations

Yaxun Sun,Xin Li,Tingting Wang,Yaxiong Ji,Yihang Yue,Yong Li,Shifeng Wang

In this study, a multi-hydroxyl-containing gemini surfactant 1,4-bis(hexadecyldimethylammonio)-2,3-dihydroxylbutane dibromide (BHHB) is firstly introduced to modify vermiculite (Na-Vt) for 2-naphthol adsorption. Successful functionalization is verified from the enhanced hydrophobicity, increased organic carbon content, enlarged interlayer spacing and decreased surface area of BHHB-Vt over Na-Vt, constructing favorable structural microenvironments for 2-naphthol retention. Effective adsorptivity and excellent reusability are obtained from the comparison of BHHB-Vt (198.16 mg/g) over Na-Vt (43.26 mg/g C0 = 300 mg/L, V = 30 mL, m = 0.03 g, t = 3 h). Partition process, hydrogen bond, OH-π interaction and electrostatic attraction are responsible for the adsorption, where OH-π interaction is stronger than hydrogen bond. The agreement of pseudo-second order and Langmuir models indicate a chemical adsorption feature on homogeneous surface. Notably, hydrogen groups connected at different carbon atoms exhibit less steric hindrance and wider molecule orbitals, providing stronger interactions between the adsorbent and targeted organic pollutant.

CAS / MDL: 1318-00-9
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Membranes · 2022 ·Vol. 12 ·期 4 ·377 · IF 4.562

Designing Multi-Stage 2 A/O-MBR Processes for a Higher Removal Rate of Pollution in Wastewater

Zhengzhong Zhou,Bin Zhang,Qian Wang,Xiaoshan Meng,Qigang Wu,Tao Zheng,Taoli Huhe

Multi-stage A/O-MBR processes were designed to improve wastewater treatment efficiency; three different designs were carried out and compared in this study. The 2(A/O)-MBR process, i.e., with two sets of anoxic/oxic tanks in series, showed better effluent quality than A/O-MBR and 3(A/O)-MBR processes. The removal rates of COD, NH4+-N, TP and TN were 95.29%, 89.47%, 83.55% and 78.58%, respectively, complying satisfactorily with China’s urban sewage treatment plant pollutant discharge standards. In terms of membrane fouling, the 3(A/O)-MBR process demonstrated the lowest fouling propensity. The microbial community structure in each bioreaction tank was analyzed, the results from which matched with the process efficiency and fouling behavior.Keywords:membrane bioreactor;wastewater treatment;microbial community;membrane fouling;multi-stage A/O

CAS / MDL: 7646-79-9
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POLYMER ENGINEERING AND SCIENCE · 2022 ·Vol. 62 ·期 11 ·3831-3840 · IF 2.573

Crystallization property, mechanical performance and enzymatic degradation behavior of PBS copolyesters modified by 2-methyl-1,3-propanediol

Sen Jiang,Liyan Wang,Rongrong Zheng,Yunsheng Chong,Yanming Chen

The poly(butylene succinate) (PBS) copolyesters modified by 2-methyl-1,3-propanediol (MPO), that is poly(butylene succinate-co-methyl propylene succinate) (PBMS), were synthesized by direct esterification-melt polycondensation method. 1 H NMR showed the PBMS molecules contain two repeating structural units, the butylene succinate (BS) and the 2-methyl-1,3-propylene succinate (MS). The crystalline properties of PBMS were characterized by DSC, POM, and XRD. The results showed the relative crystallinity of PBMS decreases from 45.12% to 38.2%, the size of spherulites also decreases, and the crystallization ability becomes weaker compared with PBS. The water contact angle test proved the surface hydrophilicity of PBMS is improved. The impact strength of PBMS increases from 3.9 to 24.6 kJ/m 2 , and its elongation at break increases from 10.5% to 71.2%, and the transition from brittle fracture to ductile fracture is achieved. The study of enzymatic degradation found that the enzymatic degradation rate of PBMS copolyesters increases significantly with the increase of MPO content. Within 25 days of degradation, the weight loss rate of PBS after degradation is 38.18%, while that of PBMS reaches 100%. Finally, it was also observed the enzymatic degradation of PBS and PBMS starts from the amorphous region and abides by the regular pattern from the periphery to the middle and from the surface to the interior.

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Polymers · 2022 ·Vol. 14 ·期 11 ·2181 · IF 4.967

Construction and Evaluation of Chitosan-Based Nanoparticles for Oral Administration of Exenatide in Type 2 Diabetic Rats

Jian-Miao Yang,Lin-Jie Wu,Meng-Ting Lin,Yi-Ying Lu,Tian-Tian Wang,Min Han,Bin Zhang,Dong-Hang Xu

Oral delivery of therapeutic peptides has been a daunting challenge due to poor transport across the tight junctions and susceptibility to enzymatic degradation in the gastrointestinal tract. Numerous advancement in nanomedicine has been made for the effective delivery of protein and peptide. Owing to the superior performance of chitosan in opening intercellular tight junctions of epithelium and excellent mucoadhesive properties, chitosan-based nanocarriers have recently garnered considerable attention, which was formulated in this paper to orally deliver the GLP-1 drug (Exenatide). Against this backdrop, we used chitosan (CS) polymers to encapsulate the exenatide, sodium tripolyphosphate (TPP) as the cross-linking agent and coated the exterior with sodium alginate (ALG) to impart the stability in an acidic environment. The chitosan/alginate nanoparticles (CS-TPP-ALG) functioned as a protective exenatide carrier, realized efficient cellular uptake and controlled release, leading to a steady hypoglycemic effect and a good oral bioavailability in vivo. Trimethyl chitosan (TMC), a chitosan derivative with stronger positive electrical properties was additionally selected as a substitute for chitosan to construct the TMC-TPP-ALG nanoparticle, and its oral peptide delivery capacity was explored in terms of both characterization and pharmacodynamics studies. Overall, our study demonstrated that functional chitosan/alginate nanoparticles can protect proteins from enzymatic degradation and enhance oral absorption, which presents important research value and application prospects.Keywords:exenatide;chitosan-based nanocarrier;sodium alginate;hypoglycemia;trimethyl chitosan

CAS / MDL: 9005-38-3
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ENVIRONMENTAL POLLUTION · 2022 · IF 9.988

Removal of lead (Pb+2) from contaminated water using a novel MoO3-biochar composite: Performance and mechanism

Yage Li,Sabry M. Shaheen,Muhammad Azeem,Lan Zhang,Chuchu Feng,Jin Peng,Weidong Qi,Junxi Liu,Yuan Luo,Yaru Peng,Esmat F. Ali,Ken Smith,Jörg Rinklebe,Zengqiang Zhang,Ronghua Li

Removal of toxic chemicals from the environment using novel adsorbents is of great concern. In this study, a novel composite of molybdenum trioxide (MoO 3 )-engineered biochar (MoO 3 -BC) was derived from corn straw and synthesized for the removal of Pb(II) from water. The pyrolysis temperature of 600 °C was suitable for the thermal self-assembly of MoO 3 -BC. Although MoO 3 -BC had lower S BET (59.3 m 2 /g) than the pristine BC (157.8 m 2 /g), it had a stronger adsorption affinity to Pb(II). The Pb(II) removal capacity of MoO 3 -BC was 229.87 mg/g at pH 4.0, and the adsorptive removal of Pb(II) was fit using a pseudo-second-order model and the Langmuir model. High temperature favored the removal of Pb(II) by MoO 3 -BC; However, the removal of Pb(II) was inhibited with increasing the ion strength. The MoO 3 -BC revealed an acceptable stability and reusability, since the removal efficiency of Pb(II) remained above 80.7%, even after 8 cycles. The MoO 3 -BC effectively reduced ≥99.9% of Pb(II) in the polluted irrigation water. The Pb(II) removal mechanisms involved surface electrostatic attraction, ion exchange and surface complexation. These findings conclude that the MoO 3 -BC is a novel composite that can be used for the removal of Pb from contaminated water . More studies are needed to investigate the potentiality of MoO 3 -biochar composite for the removal of other metals from water in a mono and competitive sorption system.

CAS / MDL: 7439-92-1
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2022 · IF 4.598

In situ mineralized Ca3(PO4)2 inorganic coating modified polyethylene separator for high-performance lithium-ion batteries

Xin Xie,Lei Sheng,Rong Xu,Xingxu Gao,Ling Yang,Yong Gao,Yaozong Bai,Gaojun Liu,Haoyu Dong,Xiaoli Fan,Tao Wang,Xianli Huang,Jianping He

The organic–inorganic composite separator possesses great thermal stability and electrolyte wettability, which is normally prepared via the slurry containing binder. However, this preparation is involved with large amounts of organic solvent that is harmful to health. In this paper, we design a novel method that combines the crosslinking technology and biomimetic mineralization process to prepare a Ca 3 (PO 4 ) 2 inorganic coating modified polyethylene separator (CaP@PE). The obtained composite separator exhibits stronger affinity to electrolyte, and its porous coating structure can store more liquid electrolyte, thus the ionic conductivity is promoted from 0.27 mS cm −1 to 0.52 mS cm −1 and the lithium-ion transference number is increased from 0.26 to 0.36. Compared with PE separator, CaP@PE separator shows better thermal stability at high temperature. Due to the improved ionic transport performance and reduced charge transfer impedance, LiCoO 2 /Li half-cell employing CaP@PE separator displays superior cycle stability and capacity retention ability after 150 cycles at a current density of 1C. Even at a high rate of 5C (7.5 mA cm −2 ), the cell with CaP@PE separator still exhibits a discharge capacity of 0.80 mAh. This work provides a promising separator to optimize the electrochemical performance and safety performance in lithium-ion battery.

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SCIENCE OF THE TOTAL ENVIRONMENT · 2022 · IF 10.753

Di-(2-ethylhexyl) phthalate increases plasma glucose and induces lipid metabolic disorders via FoxO1 in adult mice

Xiangjuan Wei,Daqian Yang,Boya Zhang,Xingpei Fan,Haining Du,Ruijiao Zhu,Xiaotong Sun,Meimei Zhao,Ning Gu

Di-(2-ethylhexyl) phthalate (DEHP), an endocrine-disrupting chemical (EDC) commonly used as a plasticizer, is responsible for widespread environmental pollution. Epidemiological and experimental data implicate DEHP and its metabolite mono(2-ethylhexyl) phthalate (MEHP) in the occurrence and development of metabolic syndrome. However, the specific effects and potential mechanisms of action of DEHP on glucose and lipid metabolism in adults are currently unclear. In the current study, adult male mice were continuously exposed to DEHP (0, 5, and 25 mg/kg/day) via oral administration and changes in glucose and lipid metabolism explored. Notably, exposure to DEHP led to a significant increase in plasma glucose and hepatic lipid accumulation but had no effect on insulin secretion. Western blot and real-time quantitative PCR showed that DEHP induced insulin resistance and promoted gluconeogenesis and lipid accumulation via overexpression of forkhead box protein O1 (FoxO1), in keeping with hepatic RNA sequencing data. Variations in gut microbiota aggravated these effects while inhibition of FoxO1 reversed the adverse effects of DEHP. Our findings support a key role of FoxO1 in disorders of glucose and lipid metabolism caused by DEHP.

CAS / MDL: 117-81-7 657-24-9
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Nano Research · 2022 ·Vol. 16 ·期 4 ·5383-5390 · IF 10.269

Ratiometric fluorescence immunoassay of SARS-CoV-2 nucleocapsid protein via Si-FITC nanoprobe-based inner filter effect

Mao Guobin,Yang Yang,Cao Shijie,Ye Silu,Li Yifang,Zhao Wei,An Hongwei,Liu Yingxia,Dai Junbiao,Ma Yingxin

The global pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus has necessitated rapid, easy-to-use, and accurate diagnostic methods to monitor the virus infection. Herein, a ratiometric fluorescence enzyme-linked immunosorbent assay (ELISA) was developed using Si-fluorescein isothiocyanate nanoparticles (FITC NPs) for detecting SARS-CoV-2 nucleocapsid (N) protein. Si-FITC NPs were prepared by a one-pot hydrothermal method using 3-aminopropyl triethoxysilane (APTES)-FITC as the Si source. This method did not need post-modification and avoided the reduction in quantum yield and stability. The p-nitrophenyl (pNP) produced by the alkaline phosphatase (ALP)-mediated hydrolysis of p-nitrophenyl phosphate (pNPP) could quench Si fluorescence in Si-FITC NPs via the inner filter effect. In ELISA, an immunocomplex was formed by the recognition of capture antibody/N protein/reporter antibody. ALP-linked secondary antibody bound to the reporter antibody and induced pNPP hydrolysis to specifically quench Si fluorescence in Si-FITC NPs. The change in fluorescence intensity ratio could be used for detecting N protein, with a wide linearity range (0.01–10.0 and 50–300 ng/mL) and low detection limit (0.002 ng/mL). The concentration of spiked SARS-CoV-2 N protein could be determined accurately in human serum. Moreover, this proposed method can accurately distinguish coronavirus disease 2019 (COVID-19) and non-COVID-19 patient samples. Therefore, this simple, sensitive, and accurate method can be applied for the early diagnosis of SARS-CoV-2 virus infection.

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CHEMICAL RESEARCH IN CHINESE UNIVERSITIES · 2022 ·Vol. 39 ·期 2 ·219-223 · IF 2.726

Electronic and Nano-structural Modulation of Co(OH)2 Nanosheets by Fe-Benzenedicarboxylate for Efficient Oxygen Evolution

Xiao Long,Wu Huirong,Zhang Yong,Sun Hao,Zhang Wenchao,Lyu Fenglei,Deng Zhao,Peng Yang

O xygen evolution reaction(OER) plays a key role in the electrochemical conversion and storage processes, but the sluggish kinetics of OER strongly impedes its large-scale applications. We herein reported the in situ growth of Fe-benzenedicarboxylate(Fe-BDC) on Co(OH) 2 nanoplates[Fe-BDC/Co(OH) 2 ] that showed remarkably enhanced OER activity than the pristine Co(OH) 2 . The incorporation of Fe species could enhance the intrinsic OER activity of Co and BDC could increase the electrochemically active surface area(ECSA), thus resulting in dramatically enhanced OER activity. In situ Raman spectroscopy characterization disclosed that Fe-CoOOH reconstructed from Fe-BDC/Co(OH) 2 was the real active site for OER. This work highlights the significance of rational tailoring of the nanostructure and electronic structure of Co(OH) 2 and provides more opportunities for its widespread applications.

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INORGANIC CHEMISTRY · 2022 · IF 5.436

Room-Temperature Synthesis of Sub-2 nm Ultrasmall Platinum–Rare-Earth Metal Nanoalloys for Hydrogen Evolution Reaction

Chaoqun Guan,Hao Chen,Hongbin Feng

To tune the activity of Pt alloy electrocatalysts and reduce the Pt loading, researchers have intensively studied alloys of Pt with late transition metals. However, Pt alloy formation with rare-earth (RE) elements through the traditional chemical route is still a challenge due to the vastly different standard reduction potentials. Here, we report a universal chemical method to prepare a series of Pt/RE (RE = La, Ce, Pr, Nd, Eu, Gd, Tb, Dy, Lu) nanoalloys with tunable compositions and ultrasmall particle sizes (sub-2 nm). These Pt–RE nanoalloys were synthesized by a strong liquid metal reduction with high-speed shearing assistance at room temperature. Among the nine Pt–RE alloy catalysts, the PtNd/C shows the best hydrogen evolution reaction (HER) activity, stability, and durability compared to commercial Pt/C. The PtNd/C shows an overpotential of 25.9 mV at the current density of 10 mA/cm2 with a Tafel slope of 19.5 mV/dec and excellent stability in the acidic medium. This work not only provides a general and scalable strategy for synthesizing noble metal–RE alloys but also highlights noble metal–RE alloys as sufficiently advanced catalysts and accelerates the research of noble metal–RE alloy in energy-related applications.

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