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SYNTHETIC METALS · 2019 · IF 2.87

Selective photoluminescence enhancement of red emitted surface modified poly(p-phenylenediamine) dots: An ultra-sensitive anion photoluminescence sensor for F− in vitro

Ye Wang,Yiwen Huang,Feiyu Wang,Jingjing Zhao,Yiming Zhang

The weak interactions between anions and common functional groups make it difficult for the development of anion photoluminescence sensors. In this work, we report an ultra-sensitive anion photoluminescence (PL) sensor for F − based on triethylene glycol monomethyl ether modified poly(p-phenylenediamine) dots (TPPDs). Due to the PET process in excited TPPDs, no obvious PL behavior can be observed in TPPDs. Due to the fast photoinduced electron transfer (PET) process in excited TPPDs, no obvious photoluminescence behavior can be observed: however, the PET process can be cut off in the presence of F − and TPPDs show bright red PL. The detection limit of this system is 2 × 10 −10 M, which is much lower than most other reported detection methods. Compared with traditional “ON-OFF” PL sensors, such an “OFF-ON” PL detection system shows higher value in practical applications. The detection system exhibits superior photostability and high selectivity for F − . We also demonstrate the successful F − detection in vitro based on TPPDs.

CAS / MDL: 106-50-3 112-35-6
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EUROPEAN JOURNAL OF INORGANIC CHEMISTRY · 2018 ·Vol. 2018 ·期 31 ·3565-3569 · IF 2.507

Fabrication of Amorphous Cu–Co–P Nanofilms on CuCo2O4 Nanoarrays by in Situ Electrochemical Reduction for Efficient Hydrogen Evolution in Alkaline Solution

Xiangjiang Zheng,Jiayu Zhang,Zhaomei Sun,Zhen Zhang,Dongmei Xi

Graphical We realized in-situ fabrication of amorphous Cu–Co–P nanofilms on CuCo 2 O 4 nanoarrays by cathodic electrochemical reduction to efficiently catalyze the hydrogen evolution reaction (HER) in alkaline solution. The catalyst needs an overpotential of only 104 mV at 20 mA cm –2 in 1.0 m KOH and presents good durability for at least 24 h. We demonstrate an efficient in-situ method to fabricate amorphous Cu–Co–P nanofilms on CuCo 2 O 4 nanoarrays by cathodic electrochemical reduction. These are used to catalyze the hydrogen evolution reaction (HER) in alkaline solution. The catalyst needs an overpotential of only 104 mV in 1.0 m KOH when the current density is 20 mA cm –2 . More importantly, it has good durability for at least 24 h. This method provides an effective approach to develop a nonprecious metal catalyst for industrial hydrogen evolution.

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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2018 · IF 4.229

Co-P nanoparticles supported on dandelion-like CNTs-Ni foam composite carrier as a novel catalyst for hydrogen generation from NaBH4 methanolysis

Fanghui Wang,Yajun Zhang,Yanan Wang,Yimeng Luo,Yuenan Chen,Hong Zhu

We used the chemical vapor deposition method to prepare dandelion-like CNTs-Ni foam composite carrier, and then the electroless plating method was used to deposit Co-P nanoparticles on the CNTs of the CNTs-Ni foam. The CNTs-Ni foam and Co-P/CNTs-Ni foam were characterized by BET, SEM, XRD , XPS , and EDS . The results showed that CNTs were uniformly and densely grown in situ on the surface of Ni foam and were further successfully coated with Co-P nanoparticles. The Co-P/CNTs-Ni foam catalysts still maintained the dandelion-like structure and reached a maximum hydrogen production rate of 2430 mL min −1  g −1 at 25 °C. Furthermore, the Co-P/CNTs-Ni foam catalysts also exhibit a remarkable cycling performance and low activation energy (49.94 kJ mol −1 ) for the methanolysis of sodium borohydride .

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POLYMERS FOR ADVANCED TECHNOLOGIES · 2018 ·Vol. 29 ·期 10 ·2665-2673 · IF 2.137

Synthesis and application of a dual functional P/N/S-containing microsphere with enhanced flame retardancy and mechanical strength on EP resin

Xiaodong Guo,Xin Wang,Xiongrui Liu,Yanyang Zheng,Jianzhong Xu,Haiyun Ma

A phosphazene derivative flame retardant with a highly cross-linked microsphere structure, named poly(cyclotriphosphazene-c-sulfonyldiphenol) (PCPS) microspheres, were synthesized by 1-pot reaction and then applied on flame retarded epoxy (EP) resin. The microstructure and chemical composition of PCPS microspheres were characterized using scanning electron microscopy, transmission electron microscopy, and element mapping. The thermal stability of PCPS microspheres and PCPS/EP composites was explored through thermogravimetric analysis. Thermogravimetric data showed that the PCPS microspheres have excellent thermal stability, and the char yield is about 43% at the end of 800°C. The incorporation of PCPS microspheres significantly increased the char yield of PCPS/EP composites. The flammability was investigated by limited oxygen index tests and cone calorimeter. The limited oxygen index value of PCPS/EP composite was increased to 29.8 from 26.6 when 3 wt% of PCPS microspheres was added. Compared with neat EP, the flame retardancy was greatly improved. The peak heat release rate and smoke production rate of PCPS/EP composites were reduced by 45.0% and 43.6%, respectively. The mechanical properties including tensile strength and modulus were both improved due to the enhancement of PCPS microspheres. The PCPS microspheres act as a dual function for improving both the flame resistance and mechanical strength of PCPS/EP system.

CAS / MDL: 80-09-1
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Journal of Physical Chemistry C · 2018 · IF 4.484

Interfacial Synergy of PtPd Nanoparticles Dispersed on Amine-Modified ZrSBA-15 in Catalytic Dehydrogenation of Ammonia Borane and Reduction of p-Nitrophenol

Zhenzhen Wang,Haoyang Zhang,Lili Chen,Songsong Miao,Shujie Wu,Xiufeng Hao,Wenxiang Zhang,Mingjun Jia

In this work, a series of amine-modified ZrSBA-15-supported PtPd bimetallic catalysts with different Pt/Pd ratios were prepared and characterized by a variety of means. Introducing amino groups on the surface of ZrSBA-15 is beneficial for achieving high dispersion of PtPd nanoparticles (NPs) and can effectively prevent the overgrowth of PtPd NPs during the preparation process. The resulting hybrid catalysts exhibit very high catalytic activity and stability for H2 generation from aqueous ammonia borane (AB) and can also efficiently catalyze the reduction of p-nitrophenol to p-aminophenol using AB as the hydrogen source. Among them, the catalyst with the Pt/Pd ratio of 85/15 shows the highest activity for AB dehydrogenation under ambient condition, whereas the catalyst with the Pt/Pd ratio of 50/50 exhibits the highest efficiency for the reduction of p-nitrophenol with AB. These results suggest that highly efficient interface active sites could be constructed by optimizing the composition of bimetallic PtPd NPs and changing the chemical surrounding of mesoporous ZrSBA-15, which demonstrate effective synergistic catalysis for AB dehydrogenation and p-nitrophenol reduction.

CAS / MDL: 13822-56-5 100-02-7
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BIORESOURCE TECHNOLOGY · 2018 · IF 5.807

Evaluation of microbial p-chloroaniline degradation in bioelectrochemical reactors in the presence of easily-biodegrading cosubstrates: Degradation efficiency and bacterial community structure

Hao Xu,Xuesong Zhao,Shaobin Huang,Han Li,Na Tong,Xiangyu Wen,Congcong Sun,Saima Fazal,Yongqing Zhang

This study aimed to illustrate p -Chloroaniline ( p -CIA) biodegradation efficiencies in bioelectrochemical reactors under stimulation by a low-voltage electric field (0.2 V versus Ag/AgCl) in the presence of easily-degrading cosubstrates including glucose and acetate. The biodegradation efficiencies of closed-circuit bioreactors were compared with those of open-circuit reactors. Experimental results showed that the six different bioreactors provided different p -CIA biodegradation efficiencies. The highest biodegradation efficiency of 38.5 ± 10.3 mg/l was obtained in a closed-circuit bioreactor with acetate and the lowest biodegradation efficiency of 15.7 ± 9.4 mg/l was obtained in an open-circuit bioreactor. This difference may be attributed to the presence of electrical stimulation and acetate. The results for generated current and biodegradation efficiency indicated that acetate is a better cosubstrate than glucose. High-throughput sequencing technologies were used to characterise the bacterial community structure of the six bioreactors and revealed that different bacterial communities resulted in different treatment efficiencies.

CAS / MDL: 106-44-5
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PHARMAZIE · 2018 ·Vol. 73 ·期 9 ·503-507 · IF 1.016

Effects of the antiretroviral drug 2'-deoxy-2'-β-fluoro-4'-azidocytidine (FNC) on P-gp, MRP2 and BCRP expressions and functions

Liu Yixian,Wang Yafeng,Peng Youmei,Liu Bingjie,Ma Fang,Jiang Jinhua,Wang Qingduan,Chang Junbiao

The purpose of the present study was to dig into recent studies designed to characterize the impacts of 2'-deoxy-2'-β-fluoro-4'-azidocytidine (FNC) on P-glycoprotein (P-gp), multidrug resistance-associated protein 2 (MRP2) and breast cancer resistance protein (BCRP). Specifically, the modulation effects of FNC on P-gp, MRP2 and BCRP protein expressions were assessed by western blot methods. 5 (and 6)-Carboxy-2',7'-dichloroflourescein (CDF) and BODIPY-prazosin were used to provide indications of alterations of MRP2 and BCRP activities. The effects of P-gp, MRP2 and BCRP on FNC were evaluated in the in situ single-pass intestinal perfusion model. The results showed that FNC at higher concentrations and with longer incubation times can upregulate the protein expression of P-gp, MRP2 and BCRP in Caco-2 cells. The upregulated proteins were also functionally active, as revealed by a lower degree of CDF and BODIPY-prazosin uptake by the cell monolayers. The intestinal absorptive coefficient (Peff) was observed to significantly increase with the inhibitors of P-gp, MRP2 and BCRP. These results suggested that FNC could modulate the expressions and functions of P-gp, MRP2 and BCRP, while P-gp, MRP2 and BCRP were involved in the efflux transport of FNC. The inductive effects of FNC on P-gp, MRP2 and BCRP suggested the possibility of FNC to contribute to the inter- and intra-individual variability of itself, as well as to alter the absorption of other drugs that may be administered concomitantly.

CAS / MDL: 57-66-9
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RSC Advances · 2015 ·Vol. 5 ·期 50 ·40000-40006 · IF 3.84

Enhanced visible-light photocatalytic activity of Ag2O/g-C3N4 p–n heterojunctions synthesized via a photochemical route for degradation of tetracycline hydrochloride

Shuaishuai Ma,Jinjuan Xue,Yuming Zhou,Zewu Zhang

Ag2O/g-C3N4 p–n heterojunctions were successfully fabricated by a facile photochemical method and applied as a photocatalyst in the degradation of antibiotic tetracycline hydrochloride (TC-HCl) under visible light irradiation. The samples were well characterized by X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), and ultraviolet-visible diffuse reflectance spectroscopy (UV-vis DRS). The results demonstrated that Ag2O nanoparticles with sizes of 5–15 nm were distributed on the surface of g-C3N4 to form the Ag2O/g-C3N4 p–n heterojunctions. The heterojunctions were conducive to the high dispersibility of small Ag2O nanoparticles and the efficient separation of photogenerated electron–hole pairs, resulting in the enhancement of photocatalytic activity by using Ag2O/g-C3N4 heterojunctions as the photocatalyst compared to pure Ag2O and g-C3N4 in TC-HCl degradation. In particular, the degradation rate of TC-HCl was 1.21 and 3.52 times higher than that of pure Ag2O and g-C3N4, respectively. Furthermore, the stability of the Ag2O/g-C3N4 photocatalyst toward the degradation process under visible light irradiation was investigated.

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NEW JOURNAL OF CHEMISTRY · 2015 ·Vol. 40 ·期 2 ·1878-1881 · IF 3.086

Solution process for fabricating CuIn0.9R0.1(S,Se)2 (R = Al, Ni, Co)/CdS p–n junctions and their applications in solar cells

Yong Cui,Zhe Zhang,Xu Du,Wei Liu,Yulin Deng,Shi Liu,Gang Wang

CuIn0.9R0.1(S,Se)2 (R = Al, Ni, Co) thin films were obtained via a solution process based on homogeneous precursor solutions and selenization. The as-prepared thin films were characterized by XRD, EDS and SEM. The CdS buffer layer was deposited by a solution process on the CuIn0.9R0.1(S,Se)2 (R = Al, Ni, Co) thin films, and Mo/CuIn0.9R0.1(S,Se)2 (R = Al, Ni, Co)/CdS/i-ZnO/ITO/Al thin-film solar cells were fabricated. The efficiencies of the as-fabricated CuIn0.9R0.1(S,Se)2 (R = Al, Ni, Co) thin-film solar cells were 4.33%, 2.38% and 1.98%, respectively.

CAS / MDL: 64-17-5 109-73-9 75-15-0
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JOURNAL OF MOLECULAR LIQUIDS · 2017 · IF 3.648

Volumetric and viscometric properties of amino acids in aqueous myo-inositol solution at T = (293.15 to 323.15) K and p = 0.101 MPa

Jing Zhang,Taotao Fu,Chunying Zhu,Youguang Ma

Densities and viscosities of glycine, L-alanine, L-valine, L-threonine and L-arginine in aqueous (0.1–0.5) mol·kg −   1 myo -inositol solutions were measured at T   =   (293.15, 303.15, 313.15 and 323.15) K and p   =   0.101   MPa. The volumetric properties such as the apparent molar volume ( V φ ), the limiting partial molar volume ( V φ 0 ), the limiting partial molar volumes of transfer (Δ tr V φ 0 ), the limiting apparent molar expansibility ( E 2 0 ), Hepler's constant and the isobaric thermal expansion coefficient ( α 2 ) were calculated through density. The viscometric properties such as the B -coefficient, the free energies of activation per mole of solvent (Δ μ 1 0   ≠ ) and solute (Δ μ 2 0   ≠ ) were obtained from the experimental viscosity data. The derived parameters hydration number and solvation number were also calculated through apparent molar volume and B -coefficient. From the volumetric and viscometric properties, the solute-solute and solute-solvent interactions in the studied systems were analyzed on the basis of co-sphere overlap model and transition state theory . Finally, the group contribution method was applied to calculate the contribution of (NH 3 + , COO − ), CH 2 , OH and CNHNHNH 2 of amino acids to V φ 0 , B -coefficient and Δ μ 2 0   ≠ .

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JOURNAL OF APPLIED POLYMER SCIENCE · 2017 ·Vol. 134 ·期 17 · IF 1.86

Improving the charged and antifouling properties of PVDF ultrafiltration membranes by blending with polymerized ionic liquid copolymer P(MMA-b-MEBIm-Br)

Chunhui Du,Xumin Ma,Jing Li,Chunjin Wu

This study describes the fabrication and properties of poly(vinylidene fluoride) (PVDF) filtration membranes modified by blending with ionic liquid block copolymer P(MMA- b -MEBIm-Br), which is synthesized via reversible addition-fragmentation chain transfer polymerization method. The attenuated total reflectance-Fourier transform infrared spectroscopy and X-ray photoelectron analyses reveal that the ionic liquid block copolymers are immobilized on PVDF membrane surface. The modified PVDF membrane exhibits excellent charged and antifouling properties because of the charged and hydrophilic properties of the copolymer. Scanning electron microscopy and atomic force microscopy also indicate the morphological characteristics of the membrane and demonstrate that the surface porous structure becomes denser after adding the copolymer. The data of filtration and the zeta potential of the membranes suggest that the charged properties of the ionic liquid block copolymers are mainly responsible for the improvement of the reversible fouling ratio and the decrease in the total fouling ratio of the membranes. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44751.

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Journal of Energy Storage · 2024 · IF 8.9

Co formic-acid framework derived CoP/Co2P heterostructures confined in N, P-doped carbon as a bifunctional electrocatalyst for zinc-air batteries

Heju Gao,Qihao Wu,Jiahui Jiang,Ting Zhao,Yuying Feng,Chunyan Wu,Guancheng Xu,Li Zhang

Reasonable construction of efficient bifunctional catalysts for the oxygen reduction reaction (ORR) and the oxygen evolution reaction (OER) counts a great deal for the development and application of rechargeable zinc-air batteries. Herein, we prepared nano-sized heterostructural particles of cobalt phosphides (CoP/Co 2 P) confined in N, P-codoped cubic through simple grinding combined with vapor deposition method using the Co formic-acid framework (Co-FF) as the precursor. Benefit from the synergistic effect between the coexistence of abundant active sites including Co sites derived the CoP/Co 2 P nanoparticles, graphitic-N, pyridinic-N species and regulation of heterojunction interface electrons, the CoP/Co 2 P@NPC-800 catalyst exhibited excellent bifunctional catalytic activity toward ORR and OER, slightly better than commercial 20 % Pt/C. The liquid zinc-air battery demonstrates a specific capacity of 720.1 mAh g −1 and outstanding stability exceeds 250 h, comparable to 20 % Pt/C. Moreover, the flexible zinc-air battery can maintain good stability under different angles of bending. This study has a certain theoretical guiding significance for the rational regulation of the phase of cobalt-based phosphide to fabricate bifunctional oxygen catalysts for metal-air battery applications.

CAS / MDL: 7440-06-4 12036-10-1
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