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PCL/PS
POLYMER ENGINEERING AND SCIENCE · 2018 · IF 1.551

Superhydrophobic PCL/PS composite nanofibrous membranes prepared through solution blow spinning with an airbrush for oil adsorption

Ju Lv,Xueqiong Yin,Rongguo Li,Junhua Chen,Qiang Lin,Li Zhu

Superhydrophobic composite nanofibrous membranes(PP) were prepared from polycaprolactone (PCL)/polystyrene (PS) through solution blow spinning with an airbrush for oil adsorption. PP membranes were characterized by fourier transform infrared spectroscopy, scanning electron microscopy, water contact angle, X-ray Photoelectron Spectroscopy, X-ray diffractometer, and thermogravimetric analysis instrument. The effects of mass ratio of PCL and PS on the morphology, porosity, density, cyrstallinity, thermal stability, and oil adsorption ability were investigated. PP membranes had higher density than PCL and PS, while better hydrophobicity. The saturation adsorption capacity of PP to peanut oil, motor oil, and diesel oil is 16.89 g/g, 20.33 g/g, and 12.17 g/g, respectively. After 6 cycles of reutilization, the adsorption capacity to peanut oil, motor oil, and diesel oil remained at 6.16, 7.46, and 5.33 g/g, respectively, higher than that of pure PCL membrane.The water/oil adsorption selectivity of PP was about 7:100. PP had higher oil adsorption capacities and better water/oil adsorption selectivity than the commercial oil absorbent polypropylene. PP membrane could be prepared and used in situ to separate oil from oil/water mixture. POLYM. ENG. SCI., 59:E171–E181, 2019. © 2018 Society of Plastics Engineers

CAS / MDL: 9003-53-6
研究领域: 材料科学 · 环境工程
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY · 2020 ·Vol. 167 ·期 11 ·110532 · IF 3.721

Hyperbranched PCL/PS Copolymer-Based Solid Polymer Electrolytes Enable Long Cycle Life of Lithium Metal Batteries

Wei Ye,Muhammad Zaheer,Lianwei Li,Jun Wang,Hongli Xu,Chaoyang Wang,Yonghong Deng

Solid polymer electrolytes (SPE) are of great importance for developing the next-generation all-solid-state lithium metal batteries, which are featured by their high safety and extraordinary energy density. Herein, by using the highly efficient azide-alkyne click chemistry, a series of long-subchain hyperbranched copolymers from various compositions of AB2 macromonomers of PCL-2N3 (polycaprolactone) and PS-2N3 (polystyrene) were synthesized and employed as SPE polymer host. Taking advantage of the hyperbranched structure, the crystallization of PCL was successfully suppressed, and endows the SPE with high ionic conductivity and high mechanical properties simultaneously. By doping with LiFSI, the SPEs thereof exhibit high ionic conductivity (1.59 × 10−4 S cm−1 at 80 °C), broad electrochemical stability window (>4.6 V) and high lithium-ion transference number (>0.40). The electrolyte film based on the HB-II (the hyperbranched PCL/PS copolymer with 70 wt% PCL and 30 wt% PS) shows an ionic conductivity of 1.36 × 10−5 S·cm−1 at 80 °C and a high lithium transference number of 0.49. The all-solid-state LiFePO4//Li cell with HB-II-based SPE delivers a high and stable discharge capacity (133 mAh·g−1 at 1 C, with 90% capacity retention after 300 cycles) and exhibits long lifetime up to over 1200 cycles, owing to its relatively high ionic conductivity and good interfacial stability.

研究领域: 材料科学 · 能源科学
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JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY · 2015 ·Vol. 54 ·期 3 ·368-380 · IF 3.113

Hyperbranched block copolymer from AB2 macromonomer: Synthesis and its reaction-induced microphase separation in epoxy thermosets

Jingang Li,Yixin Xiang,Sixun Zheng

In this contribution, we reported the synthesis of a hyperbranched block copolymer composed of poly(ε-caprolactone) (PCL) and polystyrene (PS) subchains. Toward this end, we first synthesized an α-alkynyl- and ω,ω′-diazido-terminated PCL- b -(PS) 2 macromonomer via the combination of ring-opening polymerization and atom transfer radical polymerization. By the use of this AB 2 macromonomer, the hyperbranched block copolymer ( h -[PCL- b -(PS) 2 ]) was synthesized via a copper-catalyzed Huisgen 1,3-dipolar cycloaddition (i.e., click reaction) polymerization. The hyperbranched block copolymer was characterized by means of 1 H nuclear magnetic resonance spectroscopy and gel permeation chromatography. Both differential scanning calorimetry and atomic force microscopy showed that the hyperbranched block copolymer was microphase-separated in bulk. While this hyperbranched block copolymer was incorporated into epoxy, the nanostructured thermosets were successfully obtained; the formation of the nanophases in epoxy followed reaction-induced microphase separation mechanism as evidenced by atomic force microscopy, small angle X-ray scattering, and dynamic mechanical thermal analysis. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54 , 368–380

研究领域: 高分子化学 · 材料科学 · 纳米结构功能材料 · 聚合物自组装 · 热固性树脂改性
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