KeQing Han

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Name: 韩克清; KeQing Han
Organization: Donghua University , China
Department: State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering
Title: Associate Researcher/Professor(PhD)

TOPICS

Co-reporter:Shuping Liu, Keqing Han, Lei Chen, Ying Zheng and Muhuo Yu  
RSC Advances 2015 vol. 5(Issue 47) pp:37669-37674
Publication Date(Web):24 Apr 2015
DOI:10.1039/C5RA00476D
A new method of melt-spun process was developed to prepare PAN precursor fibers using ionic liquid as the medium of processing. Melt-spun precursor fibers exhibited a partially cyclized structure. For the different structure of melt-spun precursor fibers from solution-spun precursor fibers, it is necessary to investigate the oxidation process of the melt-spun precursors. In this paper, the influence of air circulation on the structure and properties of melt-spun precursor fibers during the oxidative process was investigated by Fourier transform infrared spectroscopy, X-ray diffraction, thermogravimetry, etc.Results showed that the air circulation almost had no visible effects on the chemical structure of pre-oxidized fibers. The crystallinity and the crystal size of pre-oxidized melt-spun fibers increased with the increase of air circulation. When the air circulation was 6 L min−1, the pre-oxidized melt-spun fibers had the maximum density and tensile strength. Meanwhile, the tensile strength of the final carbon fibers reached a maximum.
Co-reporter:Shuping Liu;Lei Chen;Ying Zheng;Muhuo Yu;Jiaqi Li ;Zhao Yang
Macromolecular Materials and Engineering 2015 Volume 300( Issue 10) pp:1001-1009
Publication Date(Web):
DOI:10.1002/mame.201500104

Effects of external tension during oxidative stabilization of melt-spun polyacrylonitrile (PAN) precursor fibers on the structure and properties were investigated. The results showed that the external tension had distinct effects on the chemical and crystal structures, carbon yield, density, and tensile strength of pre-oxidized melt-spun fibers, while had little effects on elemental contents. With external tension increasing, the extent of reaction (EOR), aromatization index (AI), carbon yield, and density of pre-oxidized melt-spun fibers showed an initial increase and then a subsequent decrease, while, crystal size, crystallinity and the tensile strength appeared to first fall and then rise. When the external tension was 0.56 cN · dtex−1, the tensile strength of resulting carbon fibers reached maximum.

Co-reporter:Shuping Liu;Lei Chen;Ying Zheng ;Muhuo Yu
Polymer Engineering & Science 2015 Volume 55( Issue 12) pp:2722-2728
Publication Date(Web):
DOI:10.1002/pen.24121

Carbon fiber has many excellent properties. Currently, the precursor fiber of polyacrylonitrile (PAN)-based carbon fiber is made from solution by wet or dry spinning process that requires expensive solvents and costly solvent recovery. To solve this problem, we developed a melt-spun process with ionic liquid as the medium of processing. The melt-spun precursor fiber exhibited partially cyclized structure. The structure and properties of the melt-spun PAN precursor fiber were analyzed by combination of scanning electron microscope, Fourier transform infrared spectroscopy, differential scanning calorimetry, X-ray diffraction, thermogravimetry, ultraviolet spectroscopy, flotation technique, sound velocity orientation test, linear density, and tensile strength tests. The results showed that the tensile strength of melt-spun PAN precursor fiber was fairly high reached up to 7.0 cN/dtex. The reason was the low imperfect morphology and a cyclized structure formed by in situ chemical reaction during melt-spun process. Due to the existence of partially cyclized structure in the melt-spun PAN precursor fiber, exothermic process was mitigated and the heat evolved decreased during thermal stabilization stage in comparison with commercial precursor fibers produced by solution-spun, which could shorten the residence time of thermal stabilization and reduce the cost of final carbon fiber. POLYM. ENG. SCI., 55:2722–2728, 2015. © 2015 Society of Plastics Engineers

Co-reporter:Shuang Li;Huaiping Rong;Xuanzhe Li ;Muhuo Yu
Journal of Applied Polymer Science 2014 Volume 131( Issue 10) pp:
Publication Date(Web):
DOI:10.1002/app.40250

ABSTRACT

In this article, aramid fibers III were surface modified using an ammonia-plasma treatment to improve the adhesive performance and surface wettability. The surface properties of fibers before and after plasma treatment were investigated by X-ray photoelectron spectroscopy, scanning electron microscopy, atomic force microscopy, and water contact angle measurements. The interfacial shear strength of each aramid fibers III-reinforced epoxy composites was studied by micro-debonding test. The ammonia-plasma treatment caused the significant chemical changes of aramid fibers III, introducing nitrogen-containing polar functional groups, such as CN and CONH, and improving their surface roughness, which contributed to the improvement of adhesive performance and surface wettability. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 40250.

Co-reporter:Yue Zhang, Xinda Li, Haifeng Li, Magdi E. Gibril, Keqing Han and Muhuo Yu  
RSC Advances 2013 vol. 3(Issue 29) pp:11732-11737
Publication Date(Web):07 May 2013
DOI:10.1039/C3RA41236A
In order to prepare a cellulose-based water absorbent material in an environmentally-friendly way, a cellulose-graft-polyacrylamide (cellulose-g-PAM) copolymer is synthesized by in situ graft copolymerization through a co-rotating twin-screw extruder. An ionic liquid, namely 1-N-butyl-3-methylimidazolium chloride, is used as the reaction medium and ceric ammonium nitrate is used as the initiator. The graft copolymerization effect is evaluated by the study of the thermal and rheological properties of the copolymers. FTIR and elemental analysis results show that the amide groups of PAM successfully graft onto the cellulose backbone and the graft ratio of the cellulose-g-PAM is increased with the increase in AM content. Thermal analysis shows that the thermal stability of cellulose-g-PAM and the glass transition temperature of PAM are increased as the graft ratio increases due to the formation of PAM long-chain branches which disturb the segment motion of the cellulose chains. In comparison with cellulose, the dehydration peak of cellulose-g-PAM displays a larger endothermic enthalpy and shifts to higher temperature. Rheological results show that the storage modulus curve of cellulose-g-PAM with a high graft ratio exhibits a plateau at low frequency and the tan δ curve displays a peak value, indicating that the large amount of PAM branches cause the entanglement of copolymer chains and improve the toughness of the copolymers.
Co-reporter:Huaiping Rong;Shuang Li;Yingcai Tian;Muhuoyu
Journal of Applied Polymer Science 2013 Volume 127( Issue 3) pp:2033-2037
Publication Date(Web):
DOI:10.1002/app.37699

Abstract

A novel method is developed for grafting multiwall carbon nanotubes (MWNTs) onto the surface of polyacrylonitrile-based high strength (T300GB) carbon fiber. Functionalized MWNTs were well dispersed in the PVA solution and the carbon fiber was dip-coated in this solution. After heat treatment of the coated carbon fiber under a nitrogen atmosphere, MWNTs with carboxyl groups were grafted onto the functionalized carbon fiber via chemical interaction. The resulting materials were characterized by Fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), Field emission scanning electron microscopy (FESEM), Raman spectrum and mechanical testing. FESEM observations revealed uniform coverage of carbon nanotubes on carbon fiber. The carbon fiber grafted with MWNTs improved the tensile strength by 12% with respect to the pristine carbon fiber. These results are supportive of good interfacial bonding between the carbon nanotubes (CNTs) and carbon fiber. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013

Co-reporter:Yincai Tian, Keqing Han, Wenhui Zhang, Jingjie Zhang, Huaiping Rong, Dan Wang, Bin Yan, Shuping Liu, Muhuo Yu
Materials Letters 2013 Volume 92() pp:119-121
Publication Date(Web):1 February 2013
DOI:10.1016/j.matlet.2012.10.042
Carbon fibers have excellent properties; however, their wide application is limited by the high cost. In the production process of carbon fibers, the stabilization is the most time-consuming step. If the heat emission can be reduced or its distribution widened, it will be helpful to improve the speed of the stabilization process. In the previous article, we have reported the effect of temperature on the structure of polyacrylonitrile (PAN) in ionic liquids. In this work, influence of residence time on the structures of PAN in ionic liquids is studied by a twin-screw extruder. The formation of C=C and C=N groups was indicated by Fourier transform infrared spectroscopy (FTIR) and Ultraviolet Visible (UV–vis) absorption spectra, which was attributed to the occurrence of cyclization and dehydrogenation during the extruding process. The cyclization degree was calculated by differential scanning calorimetry (DSC) test, which can be up to 29.4% with the residence time of 40 min at 210 °C. Therefore, this method can be helpful to improve the production efficiency in the subsequent stabilization process by widening and reducing the distribution of heat emission in the product process of PAN fibers.Highlights► Effect of residence time on the structure of PAN was investigated by using a twin-screw extruder. ► Formation of C=C and C=N groups was illustrated by using FTIR and UV–vis tests. ► Degree of cyclization is up to 29.4% with the residence time of 40 min at 210 °C.
Co-reporter:Qian Huan, Shu Zhu, Yu Ma, Juanjuan Zhang, Sen Zhang, Xiaolin Feng, Keqing Han, Muhuo Yu
Polymer 2013 Volume 54(Issue 3) pp:1177-1183
Publication Date(Web):5 February 2013
DOI:10.1016/j.polymer.2012.12.055
Mechanical property of semicrystalline polymer with large-size spherulites is rather poor, and needs to be improved by adding nucleating agent to make spherulites smaller. However, the nucleating agent causes many problems limiting its applications. In this paper, we report a method to simultaneously improve the toughness and tensile strength of isotactic polypropylene (iPP) with large-size spherulites by deformation of spherulites and orientation of lamellaes through pressure-induced flow processing (PIF-processing) at solid state. The initial spherulite sizes of iPP samples with the same crystallinity and crystal form were controlled by adding nucleating agent (NA, Talc, nano-scaled), and then the samples were subjected to PIF-processing. The resulting mechanical performance of the bulk materials, including impact and tensile strength, was simultaneously enhanced. In particular, the impact strength increases upto 8 folds higher than those obtained by conventional processing for the same bulk materials, attributing to the synergistic effect of both the orientation and the large-size spherulites. The measurements of SEM, XRD and SAXS revealed the spherulites deformation and lamellae orientation during PIF-processing, as the basis of discussing the mechanism.
Co-reporter:Yue Zhang;Haifeng Li;Xinda Li;Magdi E. Gibril
Journal of Polymer Research 2013 Volume 20( Issue 6) pp:
Publication Date(Web):2013 June
DOI:10.1007/s10965-013-0171-z
With ionic liquid namely 1-N-butyl-3-methylimidazolium chloride ([BMIM]Cl) as reaction medium in cellulose modification, maleic anhydride/glycidyl methacrylate-grafted ethylene-octene copolymer (POE-g-(MA/GMA)) was blended with cellulose by a co-rotating twin-screw extruder. Cellulose/POE-g-(MA/GMA) blend was examined by FTIR, 13C-NMR, WAXD, DSC, TGA, rheology and tensile properties. Owing to the reaction between functional groups of POE-g-(MA/GMA) and hydroxyl groups of cellulose and the high mobility of POE-g-(MA/GMA), hydrogen bond network in cellulose was destructed and cellulose-b-POE-g-(MA/GMA) copolymer was synthesized in-situ. As a result, the reduction in intermolecular force of cellulose improved the melt flowability and spinnability of cellulose blend. The formation of long-chain branches hindered the crystallization and increased the thermal stability of cellulose on one hand and obtained much more chemical bond fracture under stress action and increased the tensile strength and elongation at break of the blend fibers on the other. However, the addition of 15 wt% POE-g-(MA/GMA) led to the formation of crosslined structure, so a high degree of chain entanglement increased the dynamic viscosity and decreased the spinnability of cellulose/POE-g-(MA/GMA) blend.
Co-reporter:Xi Zhao, Keqing Han, Yuqing Peng, Jia Yuan, Shutong Li, Muhuo Yu
Materials Letters 2011 Volume 65(17–18) pp:2717-2720
Publication Date(Web):September 2011
DOI:10.1016/j.matlet.2011.05.042
A novel polymeric precursor to SiBN ceramic fiber was synthesized by reaction of tetramethylaminosilane ((CH3NH)4Si) and trimethylaminoborane ((CH3NH)3B). It was shown that the polymer contains an Si―N―B bridge bond connecting the linear silicon and borazon ring parts. This structure imparts sufficient viscosity for the material to be processed by melt spinning, so that for the first time it was easily spun into green fibers using laboratory scale equipment. SiBN ceramic fibers with diameter 35 μm were obtained after pyrolysis at 1600 °C in an NH3 atmosphere. The thermal decomposition behavior of the polymer during pyrolysis was also investigated.
Poly(l-lactide)
Poly[oxy[(1S)-1-methyl-2-oxo-1,2-ethanediyl]]
Poly(lactic acid)
Steel
Cerium(IV) ammonium nitrate