JiKui Wang

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Name: 汪济奎; Wang, JiKui
Organization: East China University of Science and Technology , China
Department: Key Laboratory for Preparation and Application of Ultrafine Materials of Ministry of Education
Title: Associate Professor(PhD)
Co-reporter:Jiahong Guo, Jikui Wang, Yihan Gao, Jie Wang, Wenbo Chang, Siyuan Liao, ZiMing Qian, and YaXin Liu
ACS Sustainable Chemistry & Engineering November 6, 2017 Volume 5(Issue 11) pp:10772-10772
Publication Date(Web):October 6, 2017
DOI:10.1021/acssuschemeng.7b02734
Advanced applications of surfaces with smart wettability offer great perspectives to design novel materials. pH-responsive smart sponges with double transformation are fabricated via in situ decoration of Ag nanoparticles through an oxidation–reduction reaction and followed by modification with a mixed thiol–ethanol solution containing HS(CH2)11CH3, HS(CH2)10COOH, and HS(CH2)11OH. The wettability of sponges with optimal thiol proportions can switch reversibly between superhydrophilicity–superhydrophobicity–superhydrophilicity under different pH conditions. In addition, the as-prepared sponges have excellent absorption capacity and high oil–water separation efficiency (99.1%). This report provides a simple approach to prepare smart sponges with switchable wettability which can be further applied to many practical applications, such as marine purification and an oil–water on–off switch.Keywords: Double transformed; Oil−water separation; pH-responsive; Sponge; Thiol modification;
Co-reporter:Jiahong Guo;Sai Zhang;Xiangyan Ma;Zhoutong Qiu;Xing Peng;Jie Ying;Yuming Wang;Genhua Wu
New Journal of Chemistry (1998-Present) 2017 vol. 41(Issue 1) pp:90-96
Publication Date(Web):2016/12/19
DOI:10.1039/C6NJ03239G
A porous PDMS–PU sponge with excellent wettability was employed in this investigation for the fast absorption of oils and organic solvents. In this study, a robust superhydrophobic sponge was based on a simple dipping–coating method and HCl corrosion. The as-prepared PDMS–PU sponge possesses the advantages of convenient adsorbent collection and good recyclability. By combining the special wettability and high roughness, the sponges exhibited high absorption capacity and selectivity when used as absorptive materials for separate oil–water mixtures. Thus, these sponges show great potential for the large-scale removal of organic contaminants or oil spills from water.
Co-reporter:Sai Zhang;Jiahong Guo;Xiangyan Ma;Xing Peng;Zhoutong Qiu;Jie Ying
New Journal of Chemistry (1998-Present) 2017 vol. 41(Issue 17) pp:8940-8946
Publication Date(Web):2017/08/21
DOI:10.1039/C7NJ01067B
A smart sponge with porous structures and switchable hydrophobic–oleophilic or hydrophilic–underwater–oleophobic properties by varying the medium pH is successfully fabricated. This special sponge with a controllable wetting surface is prepared simply by introducing active hydroxyls on the surface of a fabricated poly(dimethylsiloxane) (PDMS) sponge and then esterifying it with picolinic acid. Under the synergistic action of raw PDMS chains and functionalized chains in different media the water contact angles decrease from 138° (pH = 7.0) to 10° (pH = 2.0), whereas the oil contact angles increase from 0° (pH = 7.0) to 140° (pH = 2.0) from neutral or alkaline to very acidic media underwater. The basic structure, chemical components, element type, contact angle and restorability of the sponge are also investigated. Owing to its stability and great practicability, this functionalized pH-responsive sponge can be directly used for oil/water separation. The switchable oil capture and release in aqueous media by our functionalized sponge can provide a new avenue to avoid secondary pollution in oil/water separation processes.
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Journal of Applied Polymer Science 2017 Volume 134(Issue 26) pp:
Publication Date(Web):2017/07/10
DOI:10.1002/app.45004
ABSTRACTThis study is focused on the development of high-performance composite materials based on nano silicon dioxide (nano-SiO2) modified by polydopamine (PDA). A facile one-step method was developed to synthesize core–shell structured SiO2@polydopamine (PDA) nanospheres. During the synthesis, a PDA shell was simultaneously coated on the SiO2 nanospheres to form the core–shell nanostructure which was blended with polypropylene (PP) and β nucleating agent (β-NA) to enhance both mechanical and hydrophilic properties. Nano-SiO2 particles modified by PDA (SiO2@polydopamine) influence the crystallization of PP seriously. The results indicated that when 1%wt SiO2@polydopamine was added, the impact strength of composite reached the maximum value 12.60k J/m2 increasing 137% compared with PP, the bending strength and bending modulus decreased slightly reaching 41.85 MPa, and 2192 MPa, respectively, the composite possessed hydrophilic performance with the water contact angle of 88.32°. β nucleating agent was used in all formulations, the synergistic effect toward mechanical properties with SiO2@polydopamine was studied. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017, 134, 45004.
Co-reporter:Jikui Wang, Jiahong Guo, Pengxiang Si, Wanping Cai, Yuming Wang and Genhua Wu  
RSC Advances 2016 vol. 6(Issue 6) pp:4329-4334
Publication Date(Web):21 Dec 2015
DOI:10.1039/C5RA23484K
An In(OH)3–PDMS sponge has been synthesized by covalent modification of PDA. The sponge can switch surface wettability reversibly between superhydrophobicity and superhydrophilicity when detecting ammonia. The water contact angle changes from 141.5° to 0° after storage in an ammonia atmosphere, which means an ammonia responsive surface wettability switch. The minimum NH3·H2O concentration that the In(OH)3–PDMS can detected is 5% in 2 h. This kind of quick and sensitive ammonia detector is promising simply by virtue of the surface wettability conversion.
Co-reporter:Shenzhe Li;Yinyin Li;Genhua Wu;Yuming Wang;Wenqi Wang;Jiahong Guo
Journal of Applied Polymer Science 2016 Volume 133( Issue 44) pp:
Publication Date(Web):
DOI:10.1002/app.44126

ABSTRACT

A novel poly(acrylonitrile-co-butadiene-co-styrene) (ABS) antistatic and flame-retardant agent, poly(ethylene glycol) methacrylate/methyl methacrylate/diethyl allylphosphonate (PMMD), was synthesized from poly(ethylene glycol) methacrylate, methyl methacrylate, and diethyl allylphosphonate by free-radical precipitation polymerization in the aqueous phase to improve the antistatic and flame-retardant performance at the same time. Through adjustments of the molar ratios of the three monomers, various antistatic, flame-retardant copolymers (PMMD) were synthesized. The molecular structure and thermal stability of PMMD were analyzed with Fourier transform infrared spectroscopy and thermogravimetric analysis. The electrical resistivity and flame-retardant and mechanical properties of the ABS/PMMD composites were analyzed by a ZC90 megohmmeter, an oxygen index meter, a vertical burning tester, a memory impact testing machine, and a tensile testing machine. The morphology of PMMD in the ABS blends was characterized with scanning electron microscopy. The compatibilities of PMMD and ABS were characterized by the calculation of the thermodynamic work of adhesion via the measurement of the contact angle. The results show that the antistatic and flame-retardant performance of ABS were greatly improved by the PMMD copolymer and the mechanical properties of ABS showed little reduction. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016, 133, 44126.

Co-reporter:Pengxiang Si;Cong Zhao;Heng Xu;Kun Yang;Wenqi Wang
Polymers for Advanced Technologies 2015 Volume 26( Issue 9) pp:1091-1096
Publication Date(Web):
DOI:10.1002/pat.3538

This study described an approach to impart controlled morphology and improved pore interconnectivity to poly(dimethylsiloxane) (PDMS) sponges for oil sorption by partially fusing the sugar particles together prior to creation of a continuous PDMS matrix. PDMS sponges with high absorption capacity, low water pickup, and remarkable reusability were fabricated by the polymerization of the PDMS prepolymer and a curing agent in cyclohexane. The PDMS sponge showed oil absorbency in the range from 790% to 4000% for various oils solvents, with the maximum absorption capacity reaching up to 23 times of its weight. Compressive modulus of PDMS subjected to sugar fusion for 24 hr was significantly increased to 1900 Mpa. The sponge also exhibited excellent repellency to corrosive strong acid and alkali. Besides, oil can be quickly adsorbed in tens of seconds and maintained for several months. Furthermore, PDMS sponges showed little loss of their absorption capacities and owned weights after 20 absorbing/recovering cycles. Copyright © 2015 John Wiley & Sons, Ltd.

Co-reporter:Kai Wu, ;Fangqin Lin;Yanchang Liu;Kun Yang;Xu Zhou ;Diqi Zhang
Polymer Composites 2014 Volume 35( Issue 9) pp:1716-1722
Publication Date(Web):
DOI:10.1002/pc.22825

The polyvinyl chloride (PVC)/thermoplastic polyurethane (TPU) foam composite was modified by glycidyl methacrylate (GMA) innovative and prepared by sheet molding method with foaming agent azodicarbon amide (AC) and crosslinking agent bis-tert-butylperoxy diisopropylbenzene (BIPB). The properties of PVC/TPU foam composites effected by GMA content were investigated by the density, impact, tensile, and flexible test. The experiment indicated that with the addition of GMA, the impact strength tensile strength and flexible modulus were firstly rose to maximum at a fast rate and then decreased slightly. The properties significantly increased at a low content of modifier GMA. The results observed by differential scanning calorimetry indicated that new crosslinking network between PVC and TUP formed after the addition of GMA. The foam quality and cell morphology were studied by SEM and then statistics. With the addition of 0.6 phr BIPB and 0.5 phr GMA, the cell size of PVC/TPU composite is 80–130 μm and cell wall is 10–15 μm. Furthermore, the cells have more uniform distribution and fewer collapse when compared with the material without GMA. POLYM. COMPOS., 35:1716–1722, 2014. © 2013 Society of Plastics Engineers

Co-reporter:Yanan Nie;Xiaocai Tian;Yanchang Liu;Kai Wu
Polymer Composites 2013 Volume 34( Issue 1) pp:77-87
Publication Date(Web):
DOI:10.1002/pc.22379

Abstract

A new corn starch adhesive modified by starch-g-polyvinyl acetate (starch-g-PVAc) and epoxy resin is described in this study. Starch-g-PVAc is used as high cohesive energy component to improve the dry shear strength of the starch adhesive. Although the epoxy resin, which can easily crosslink with the oxidized starch, is used as water-resistant component to improve the wet shear strength. Because there is no chemical reaction happening between polyvinyl acetate and epoxy resin, both the dry shear strength and the wet shear strength of the corn starch adhesive are notably increased. Considering all the related factors, the optimum of the modification is achieved when the dosage of starch-g-PVAc and epoxy resin is 70% of the oxidized starch latex with m(Ep): m(starch-g-PVAc) = 1:2. That is, the epoxy resin is 23% in mass fraction and starch-g-PVAc 47% in mass fraction. The dry shear strength is 4.50 MPa, and the wet shear strength is 2.51 MPa. The modified corn starch has a broad prospect in the application of plywood industry. POLYM. COMPOS., 2013. © 2012 Society of Plastics Engineers

Co-reporter:Wei Wang;Guixin Zhang;Weizhou Zhang
Journal of Polymers and the Environment 2013 Volume 21( Issue 1) pp:46-53
Publication Date(Web):2013 March
DOI:10.1007/s10924-012-0505-7
Fully-biodegradable and highly-filled thermoplastic starch plasticized with glycerol (GTPS)/poly (butylene succinate) (PBS) blends were prepared by Haake Mixer. Processing properties, thermal behaviors including melting and crystallization behavior, crystal structure, and compatibility of the blends were investigated using differential scanning calorimeter (DSC), wide angle X-ray diffractometer (WAXD), scanning electron microscopy (SEM) and dynamic mechanical analysis (DMA). The maximum and equilibrium torques decreased with the rising of glycerol contents and the dropping of PBS contents. GTPS30/PBS blends exhibited double melting endothermic peaks in the DSC thermograms, which related to the crystallization behavior and compatibility of the blends, but no double peaks for GTPS40/PBS. The addition of starch and glycerol could lead to higher crystallinity and lower crystallization rate of PBS, but would not change the crystal types and crystallite sizes of PBS according to DSC and WAXD analysis. SEM and DMA results gave the evidence to confirm the better compatibility of GTPS40/PBS. Besides, higher storage modulus in glassy state of GTPS/PBS blends than PBS could be seen from DMA analysis, which was the contrary in rubbery state.
Co-reporter:Q. F. Shi;H. Y. Mou;Q. Y. Li;J. K. Wang;W.H. Guo
Journal of Applied Polymer Science 2012 Volume 123( Issue 5) pp:2828-2836
Publication Date(Web):
DOI:10.1002/app.34807

Abstract

Influence of heat treatment and fillers on the heat distortion temperature (HDT) of poly(lactic acid) hybrid biocomposites was intensively studied through HDT testing, polarizing microscope (POM), differential scanning calorimetry (DSC), and dynamic mechanical analysis (DMA). With loading 20 wt % BF or 20 wt % talc, improvement of HDT in PLA composite was about 10°C comparing with neat PLA after heat treatment. Moreover, there was a great improvement (above 45°C) of HDT in PLA composites with loading 20 wt % BF and 20 wt % talc simultaneously after heat treatment. Transcrystallization was observed during heat treatment and isothermal crystallization of PLA composites with loading BF and talc simultaneously. There was no similar phenomenon in other PLA composite with loading only one filler. The possible mechanism of forming transcrystallization was proposed. DSC and DMA were also used to clarify the variation in HDT before and after heat treatment, and the results suggest that the crystallinity, modulus and glass transition changed, especially formation of transcrystallization played a key role in improvement of HDT in PLA composites. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012

Co-reporter:Jikui Wang;Guofeng Cai;Xudong Zhu ;Xiaping Zhou
Journal of Applied Polymer Science 2012 Volume 124( Issue 1) pp:109-115
Publication Date(Web):
DOI:10.1002/app.35045

Abstract

The oxidative chemical polymerization of 3, 4-ethylenedioxythiophene (EDOT) was conducted at room temperature in the presence of poly(styrene sulfonate) (PSS) as the doping agent, sodium supersulphate (Na2S2O8) and ferric sulphate(Fe2(SO4)3) as the compound oxidant and deionized water as the solvent. In order to remove sodium ion (Na+), ferric ion (Fe3+), and sulfate ion (SO42−), certain amount of ion exchanger was added after 24 h, the dark blue poly(3, 4-ethylenedioxythiophene) (PEDT)/PSS solution was obtained. The influence of different proportions of EDOT and PSS, different proportions of EDOT and the compound oxidant, different stirring rates on the morphology, and surface resistivity were discussed. The influence of pH value of the PEDT/PSS solution, the coating thickness, and soak time on the surface resistivity was investigated. Recipe and experimental conditions were optimized and the PEDT/PSS solution was obtained with excellent performance which has relatively low in surface resistance, good water tolerance, and light transmittance. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012

Co-reporter:Xu Zhou, Guixin Zhang, Weizhou Zhang, Weihong Guo and Jikui Wang
Polymer Journal 2012 44(5) pp:382-387
Publication Date(Web):March 14, 2012
DOI:10.1038/pj.2012.6
Organic hybrids of polyacrylate emulsion (PAE)/hindered phenol (3,5-bis(1,1-dimethylethyl)-4-hydroxybenzenepropanoic acid thiodi-2,1-ethanediyl ester, abbreviated as Irganox-1035) have been prepared in this study. The dynamic mechanical properties, denoted by storage modulus (E′) and loss factor (tanδ), of this binary system have been investigated. Dynamic mechanical analysis (DMA) results show that by adding Irganox-1035, the tanδ peak maximum of the hybrids are remarkably increased up to 4.2, demonstrating PAE/Irganox-1035 hybrids are promising damping materials. The damping mechanism of the hybrids has also been systematically investigated through Fourier transform infrared spectroscopy (FTIR), differential scanning calorimeter (DSC), X-ray diffraction (XRD), DMA and scanning electronic microscope (SEM). The experimental results indicate no hydrogen bonding is formed between polyacrylate matrix and Irganox-1035 molecules and PAE has a good compatibility with Irganox-1035 existing in the amorphous form in the hybrids. Meanwhile, DMA results show amorphous Irganox-1035 has a super-high viscoelastic property (tanδ=20.7), which improves the damping performance of this compatible hybrids system.
Co-reporter:Yishu Fu;Guang Zhao;Yaoxian Wang ;Shujun Chen
Journal of Applied Polymer Science 2011 Volume 122( Issue 1) pp:12-18
Publication Date(Web):
DOI:10.1002/app.33265

Abstract

A novel antistatic agent poly(ether-ester-amide) (PEEA) based on caprolactam, polyethylene glycol, and 6-aminocaproic acid was successfully synthesized by melting polycondensation. The structure, thermal properties, and antistatic ability of the copolymer were characterized by Fourier transform infrared spectroscopy, differential scanning calorimetry, thermogravimetric analyses, and ZC36 megohmmeter. Test results show that PEEA is a block copolymer with a melting point of 217°C and a thermal decomposition temperature of 409°C, together with a surface resistivity of 108 Ω/sq. Antistatic poly(acrylonitrile-co-butadiene-co-styrene) (ABS) materials were prepared by blending different content of PEEA to ABS resin. The antistatic performances, morphology, and mechanical properties were investigated. It is indicated that the surface resistivity of PEEA/ABS blends decrease with the increasing PEEA content, and the excellent antistatic performance is obtained when the antistatic agent is up to 10–15%. The antistatic performance is hardly influenced by water-washing and relative humidity, and a permanent antistatic performance is available. The antistatic mechanism is investigated. The compatibility of the blends was studied by scanning electron microscopy images. The ladder distribution of antistatic agent is formed, and a rich phase of antistatic agent can be found in the surface layer. The elongations at break of the blend are improved with the increasing antistatic agent; the tensile strength and the notched impact strength kept almost the same. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011.

Co-reporter:Guofeng Cai;Yanan Nie;Xiaocai Tian;Xudong Zhu ;Xiaping Zhou
Polymer Composites 2011 Volume 32( Issue 12) pp:1945-1952
Publication Date(Web):
DOI:10.1002/pc.21223

Abstract

Three kinds of reactive toughening agents of bamboo plastic composites are studied in this article. The bio-fiber keeps high polarity for the hydroxyl groups of the surface, while polypropylene (PP) matrix resin phase is nonpolar. So, the interfacial compatibility between matrix and enhanced phase is poor. The anhydride in maleic anhydride grafted polypropylene can react with the hydroxyls. A large number of hydroxyl groups on the fiber surface are reduced, and the interfacial bond strength is improved. Three reactive toughening agents: glycidyl methacrylate grafted poly(ethylene-1-octene), maleic anhydride grafted poly(ethylene-octene), and poly(ethylene-butylacrylate-glycidyl methacrylate) are chosen to improve the impact toughness. The mechanical properties, compatibility, phase structure, water absorption, and thermal properties of PP blends are all investigated. When the content of toughening agents are controlled between 6% and 8%, not only the impact strength is greatly improved but also the other properties of PP are less affected, which makes the composites with comprehensive and practical applications. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers

Co-reporter:Shuangming Mao;Chunchang Qiu;Weihong Guo ;Yaoxian Wang
Journal of Applied Polymer Science 2010 Volume 116( Issue 6) pp:3455-3459
Publication Date(Web):
DOI:10.1002/app.31871

Abstract

Modified polypropylene was prepared by blending with potassium titanate whisker (PTW) and 10 w/w% talc via Haake extruder followed by injection molding. Reinforced with both PTW and talc, the PP composites exhibited better mechanical properties. The tensile modulus and flexural modulus of PP composites tend to increase with the increasing of whisker concentrations. The talc plays a synergistic role in improving the mechanical properties of composites and reducing cost. Torque measurement shows the PP composites has a good processing condition due to lubrication of PTW. TGA test shows PP composites containing 20 w/w% PTW and 10 w/w% talc is useful for improving PP composite's thermo oxidative stability. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010

Co-reporter:Chunchang Qiu;Shuangming Mao;Weihong Guo;Shujun Cheng ;Yaoxian Wang
Polymers for Advanced Technologies 2010 Volume 21( Issue 9) pp:651-655
Publication Date(Web):
DOI:10.1002/pat.1482

Abstract

Poly(3, 4-ethylenedioxythiophene)/poly(styrene sulfonate) (PEDT/PSS) composite is prepared by solution polymerization at room temperature in the presence of 3, 4-ethylenedioxythiophene as the monomer, PSS as the doping agent, potassium supersulfate (KPS) as the oxidant, and deionized water as the solvent. The color of the PEDT/PSS solution is dark blue and its solid content is 2.2%, its pH value is 1.5. By mixing alcohols, polar organic solvents, adhesives, and so on into PEDT/PSS solution, the anti-static coating solution is prepared. The coating is conducted by bar-coating (20 µm) at 40% relative humidity and 20°C. The influence of the content of each component on the coating surface resistivity is discussed, and a reasonable volume content of each component is obtained. The obtained coating has low surface resistivity (1 × 106 Ω), excellent water resistance, and high transmittance of visible light together with a wide range of potential applications. Copyright © 2009 John Wiley & Sons, Ltd.

2-?Propenoic acid, 2-?methyl-?, 2-?oxiranylmethyl ester, polymer with formaldehyde, graft
Ethanaminium, N,?N,?N-?trimethyl-?2-?[(2-?methyl-?1-?oxo-?2-?propen-?1-?yl)?oxy]?-?, chloride (1:1)?, polymer with ethenylbenzene and sodium 4-?ethenylbenzenesulfon?ate (1:1)
poly(ethylene glycol) methyl ether meth-acrylate