JOURNAL OF APPLIED POLYMER SCIENCE
·
2019
·Vol. 136
·期 46
·48237
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IF 2.188
Feng Gao,Yifang Mi,Xinlei Wu,Jun Yao,Qi Qi,Zhihai Cao
Stimuli-responsive polymeric nanogels hold great potential in biological applications. In this work, thermoresponsive polymeric nanogels were conveniently prepared through inverse miniemulsion polymerization of two monomers with a good biocompatibility, N -vinylcaprolactam and 2-methoxyethyl acrylate. A macromolecular crosslinker, poly(ethylene glycol) dimethacrylate (PEGDMA), was used to achieve a better thermoresponsiveness, compared with low-molecular-weight crosslinkers. The prepared poly( N -vinylcaprolactam- co -2-methoxyethyl acrylate) (poly(NVCL- co -MEA)) nanogels could be well redispersed in aqueous systems, displaying a reversible thermoresponsive transition behavior. The influences of the synthesis parameters including the emulsifier content, PEGDMA content, and monomer composition on the particle properties of poly(NVCL- co -MEA) nanogels both in inverse emulsions and in aqueous dispersions were systematically investigated. Furthermore, the impacts of the monomer composition and PEGDMA content on the thermoresponsiveness of poly(NVCL- co -MEA) nanogels were also studied. Promisingly, the introduction of MEA monomeric units to the copolymer chains only slightly reduced the thermoresponsiveness of poly(NVCL- co -MEA) nanogels. This feature allows to improve the biocompatibility of polymeric nanogels by using MEA as the comonomer without need to compromise the thermoresponsiveness of nanogels. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136 , 48237.
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JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY
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2019
·Vol. 321
·期 3
·895-905
·
IF 1.186
Jiang Zhipeng,Xie Fan,Kang Chuanhong,Wang Yanfei,Yuan Long,Wang Yue
Poly(cyclotriphosphazene- co -4,4′-diaminodiphenyl ether) microspheres (PZA) was based on hexachlorocyclotriphosphazene (HCCP) and 4,4′-diaminodiphenyl ether (ODA). It was synthesized via one-step precipitation method. The PZA microspheres were characterized by FT-IR, XPS, zeta potential and SEM/EDS. Through experimental research, PZA microspheres had the optimal adsorption performance with pH value 3.5, contact time of 60 min, thorium(IV) ions concentration of 30 mg L −1 , and PZA microspheres of 10 mg. The maximum adsorption capacity of PZA microspheres for thorium(IV) was 29.04 mg g −1 . The adsorption process could be described by the quasi-second order kinetic model and simulated by the Langmuir isotherm equation.
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ADVANCED SYNTHESIS & CATALYSIS
·
2019
·Vol. 361
·期 15
·3525-3531
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IF 5.451
Jitao Wang,Xiaochun Yu,Chongyang Shi,Dajie Lin,Jun Li,Huile Jin,Xian Chen,Shun Wang
A facile fabrication of Fe and N co-doped mesoporous carbon (MC), as an efficient heterogeneous catalyst for the highly selective reduction of nitroarenes, is described. The Fe and N co-doped MC nanosheets are easily synthesized via a hydrothermal reaction between citrate acid and magnesium citrate, followed by calcination in the presence of melamine and potassium ferrocyanide. The Fe−N complex provides a unique active site for the selective reduction of 1-chloro-4-nitrobenzene, leading to the production of (E)-1,2-bis(4-chlorophenyl)diazene with a selectivity of >96%, in <40 mins. Control experiments based on non-doped, N-doped, and Fe-doped MC nanosheets demonstrate that selectivity greatly depends on the catalyst active component type, and that non-doped MC significantly contributes to the high efficiencies observed in the selective synthesis of azoxy compound intermediates. A broad range of substrates, including extra-functional groups on the nitroarenes rings, were successfully converted to the corresponding azo compounds at mild conditions with high selectivity.
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DALTON TRANSACTIONS
·
2018
·Vol. 48
·期 3
·891-897
·
IF 4.099
Bing Chang,Yingchun Yang,Zhixiang Ye,Shengyu Liu
Hydrogen is the most attractive source of energy in the 21st century. However, high-efficiency mass production of hydrogen still faces many challenges. Although electrochemical water splitting is an ideal way to produce hydrogen, it requires low-cost and efficient electrocatalysts. In this work, a hybrid shell/core Co–P/CuO nanowire array was fabricated by Co–P film electrodeposition on a CuO nanowire array. Because of the synergy between Co–P and CuO nanowire arrays, Co–P/CuO shows remarkable activity toward the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER). This bifunctional electrocatalyst achieving 20 mA cm−2 requires a cell voltage of only 1.645 V, and has superb long-term electrochemical stability and high faradaic efficiency.
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高影响因子
APPLIED SURFACE SCIENCE
·
2018
·
IF 4.439
Xudan Li,Hanwei He
Cobalt hydroxide nanosheets/ruthenium oxide (Co(OH) 2 /RuO 2 ) nanocomposite on nickel foam was successfully synthesized via a simple electrodeposition process as an advanced supercapacitor electrode material. The microscopy studies reveal that RuO 2 nanoparticles are loaded uniformly on interconnected Co(OH) 2 nanosheets forming a three-dimensional (3D) network. The performance optimization of composite is come true through adjusting deposition time of RuO 2 nanoparticles. The electrochemical tests indicate that the optimized Co(OH) 2 /RuO 2 nanocomposite displays excellent super-capacitive properties. The specific capacitance is up to 2168 F g −1 as the current density is 1 A g −1 . Compared with the pure Co(OH) 2 and RuO 2 , the capacitance of the Co(OH) 2 /RuO 2 composite increases by 57% and 80%, respectively. The capacitance maintains at 86.0% after 5000 charging and discharging loops at the constant current density of 5 A g −1 , while the pure Co(OH) 2 only maintains 71.7% of the original capacitance after 5000 loops. The asymmetric capacitor assembled using Co(OH) 2 /RuO 2 nanocomposite as positive electrode and activated carbon (AC) as negative electrode exhibits a high energy density of 58.4 W h kg −1 at a power density of 1.2 kW kg −1 . The good pseudocapacitance behavior of the Co(OH) 2 /RuO 2 composite is mainly in virtue of the good synergies between Co(OH) 2 and RuO 2 insuring large surface area, rich electrochemical reactive sites, the short diffusion pathways of ions and good electroconductivity during the charge-discharge process.
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ACS Applied Materials & Interfaces
·
2018
·
IF 8.097
Xiangdong Xu,Hongliang Zeng,Dezhi Han,Ke Qiao,Wei Xing,Mark J. Rood,Zifeng Yan
Sodium-ion batteries (SIBs) attract more attention because of sodium’s abundant availability, affordable price, and potential to be an effective anode material. Meanwhile, carbon-based materials provide the most promising anode materials. Because of the large radius of sodium ions, SIBs do not exhibit favorable electrochemical performance. Introducing heteroatoms into the carbon-lattice is an effective strategy to enlarge the interlayer space of carbon-based materials which can improve carbon’s electrochemical performance. In addition, anode materials with a surface-induced capacitive process can enhance the SIB’s electrochemical performance because its capacitive process increases the kinetics of ion diffusion. Here, we describe an SIB’s anode material containing nitrogen and sulfur co-doped graphene sheets [denoted as poly(2,5-dimercapto-1,3,4-thiadiazole) (PDMcT)/reduced graphene oxide (RGO)] which are synthesized via carbonization of PDMcT polymerized on the surface of GO. PDMcT/RGO exhibited high capacities (240 mA h g–1 at 500 mA g–1), improved rate performance (144 mA h g–1 at 10 A g–1), and good cycling stability (153 mA h g–1 after 5000 cycles at 5000 mA g–1). These unique results are attributed to the enlarged interlayer spacing and electronic conductivity from the heteroatoms which facilitate the sodium ion’s insertion and electron transport. These results represent that PDMcT/RGO is a great potential anode material for SIBs.
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ACS Applied Materials & Interfaces
·
2018
·
IF 8.097
Yangqin Gao,Yandong Li,Guoqing Yang,Songsong Li,Nan Xiao,Boran Xu,Shuang Liu,Ping Qiu,Shijie Hao,Lei Ge
Fe2TiO5 was synthesized via the solvothermal method and adopted as co-catalyst to improve the photoelectrochemical (PEC) water splitting performance of BiVO4 photoanode. After surface modification by Fe2TiO5, the BiVO4/Fe2TiO5 photoanode shows a 300 mV cathodic shift in onset potential and 3 times enhancement in photocurrent, which delivers a photocurrent density of 3.2 mA/cm2 at 1.23 V vs reverse hydrogen electrode. Systematic optical, electrochemical, and intensity-modulated photocurrent spectroscopy characterizations were performed to explore the role of Fe2TiO5 and reveal that the enhanced PEC performance is mainly caused by the surface passivation effect of Fe2TiO5.
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ACS Applied Materials & Interfaces
·
2018
·
IF 8.097
Chen Jiao,Yuanyuan Chen,Tianqi Liu,Xin Peng,Yaxin Zhao,Jianan Zhang,Yuqing Wu,Huiliang Wang
Shape memory hydrogels (SMHs) have a wide range of potential practical applications. However, the mechanically weak and soft nature of most SMHs strongly impedes their applications. Here, we report a novel kind of thermal-responsive SMH with high tensile strength and high elastic moduli. Organogels are first prepared by the copolymerization of a hydrophilic monomer N-vinylpyrrolidone (NVP) and a hydrophobic monomer acryloxy acetophenone (AAP) in N,N′-dimethylformamide (DMF) solutions, and then, poly(vinylpyrrolidone-co-acryloxy acetophenone) [poly(NVP-co-AAP)] hydrogels are obtained by solvent exchange with water. Because of the strong and reversible hydrophobic association and π–π stacking of acetophenone groups, the poly(NVP-co-AAP) hydrogels exhibit tensile strengths up to 8.41 ± 0.83 MPa and Young’s moduli up to 94.2 ± 1.3 MPa, which are more than 1 or 3 orders of magnitude higher than those of the organogels, respectively. The poly(NVP-co-AAP) hydrogels exhibit good shape memory behaviors, with a complete fixation ratio and a recovery ratio of 74–89%, as well as very fast shape-fixing and recovering rates (in seconds). These rigid and strong hydrogels are demonstrated to be an ideal shape memory material for surgical fixation devices to wrap around and support various shapes of limbs.
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APPLIED SURFACE SCIENCE
·
2018
·
IF 4.439
Bangbang Wang,Enzhu Hu,Zhiqiang Tu,Karl Dearn David,Kunhong Hu,Xianguo Hu,Wei Yang,Jianhua Guo,Weimeng Cai,Wenli Qian,Hao Zhang
A novel carbon nanoparticle co-doped with sulfur and nitrogen (S, N CN) was prepared from rice husk powder through a hydrothermal reaction. A series of modern analysis techniques was utilized to characterize the morphology, structure, and components of the S, N CN nanoparticles. Their tribological properties as a lubricating additive to polyethylene glycol (PEG200) base oil were investigated using a UMT-2 sliding tribometer. Results showed that the average diameter of nanoparticles were approximately 16 nm. The nanoparticles mainly included C, O, N, and S. The I D /I G value of S, N CN was 2.63. PEG200 that included different contents of S, N CN displayed remarkable lubricating performance compared with pure PEG200 under different loads (8, 20, 40, and 100 N). When 0.1 wt% S, N CN was dispersed in base oil, the friction coefficient and wear rate decreased by 16.6% and 75.9%, respectively. The friction and wear mechanisms were attributed to robust tribo-films that had developed as a result of tribo-chemical reactions induced by the S, N CN particles, comprising nitrides, sulfides, and metal oxides to promote wear resistance and friction reduction properties of PEG200.
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CATALYSIS TODAY
·
2018
·
IF 4.667
Xiao Dong,Peng Zheng,Ai-Guo Zheng,Hui-Feng Li,Guo-Fu Xia,Ming-Feng Li,Ren-Yang Zheng,Bo-Qing Xu
Pt-Co/SiO 2 and Pt-Ir-Co/SiO 2 catalysts were prepared via galvanic replacement (GR) and employed for the hydrogenolytic ring-opening of methylcyclopentane (MCP). Selective deposition of the noble metals at the less expensive Co nanoparticle (NP) surface by GR greatly enhanced the utilization efficiency of the more active Pt or Pt and Ir atoms for the selective catalysis to the ring-opening reaction of MCP, as justified by comparison with catalysts from conventional impregnation preparation. The chemistry of GR was quantitatively studied by comprehension of the composition changes both in the preparation solution and in the solid samples. The structural features of GR catalysts were characterized as highly dispersed Pt or Pt and Ir clusters selectively deposited on Co NP surface. Compared to their counterparts from impregnation preparation, the GR catalysts showed much higher mass-specific activity normalized by overall noble metal loading (MSA NM ), due to the significantly enhanced utilization efficiency of Pt or Pt and Ir. In addition, the trimetallic Pt-Ir-Co/SiO 2 catalyst showed a distinctly higher MSA NM than the bimetallic Pt-Co/SiO 2 and Ir-Co/SiO 2 ones. This observation features a synergy between the highly dispersed Pt and Ir clusters in the catalysis, besides the enhanced noble metal utilization efficiency. Our catalytic data seem to suggest that a dicarbene mechanism was prevailing over the GR catalysts for the ring-opening reaction of MCP.
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RSC Advances
·
2018
·Vol. 8
·期 20
·11119-11126
·
IF 2.936
Faqin Tong,Shuangshuang Chen,Zhao Chen,Xuemin Lu,Qinghua Lu
Enhancing the azimuthal anchoring energy of the aligning film is a key requirement to improve the quality of liquid-crystal displays. Based on the assumption of mesogenic side groups being able to align liquid-crystal (LC) molecules, we have designed a novel transparent polyimide bearing cyanobiphenyl mesogenic side chains, which has a similar structure to that of liquid crystal 5CB. A pyrimidyl diamine monomer with a cyanobiphenyl mesogenic unit was first synthesized, and then co-polymerized with 4,4′-diaminodiphenyl ether and 4,4′-oxydiphthalic anhydride. The obtained polyimide (PI) exhibited good thermal stability and mechanical properties, as well as high optical transparency with transmittance of up to 86% in the wavelength range 450–700 nm. By evaluating the adhesion force between PI films and LCs with a super-sensitive microelectro-mechanical balance system, we have verified that appending mesogenic groups on the side chains of PI strengthens intermolecular interactions between the LC and PI surfaces, thereby enhancing the surface anchoring energy. Compared with the unmodified PI, the anchoring energy of the derivatized PI was improved more than 2.2-fold. By virtue of its good transparency and strong anchoring energy, this PI would seem to be an ideal candidate as a LC alignment film, and the concept of mesogens aligning LCs may open a new door in the design of LC alignment films.
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DESIGNED MONOMERS AND POLYMERS
·
2015
·
IF 2.78
Guang-Zhen Mo,Yan-Cheng Wu,Zhi-Feng Hao,Qiao-Fang Luo,Xin-Yu Liang,Li-Tao Guan,Zhao-Yang Wang
Using aminomethyl benzimidazole (AMB) as a model of benzimidazole-type drugs, a potential biodegradable drug-loaded polymer poly(lactic acid-co-aminomethyl benzimidazole) (PLAAMB) is synthesized as designed via direct melt polycondensation starting from d,l-lactic acid (LA). When the molar feed ratio LA/AMB is 40/1, the optimal synthetic conditions, including catalyst type and dosage, polycondensation temperature, and copolymerization time are discussed. After the prepolymerization at 140 °C for 8 h, using 0.4 wt% stannous oxide (SnO) as the catalyst, the melt copolymerization at 160 °C for 6 h gives the copolymer with the biggest weight-average molecular weight (Mw) 5300 Da. The structure and properties of the copolymer are systematically characterized with Fourier transform infrared, 1H NMR, gel permeation chromatography, differential scanning calorimetry, and X-ray diffraction. And the investigations on the influences of different molar feed ratios on the properties of PLAAMB show that, the copolymer PLAAMB with the biggest Mw of 9400 Da can be obtained. After the drug model AMB as a monomer is introduced into polylactic acid during the condensation, the Tg of the obtained PLAAMB is lower than the Tg of homopolymer poly(d,l-lactic acid) (PDLLA). The Mw and crystallinity of PLAAMBs can meet the requirement of drug-loaded polymers in the drug delivery.
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