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“LIVING”/CONTROLLED RADICAL POLYMERIZATION OF ETHYL METHYLACRYLATE WITH 2,2’-AZOBISISOBUTYRONITRILE/FERRIC CHLORIDE/TRIPHENYLPHOSPHINE INITIATION SYSTEM

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Chinese Journal of Polymer Science 2000年第2期18卷 149-153页

作者： Xiao-ping Chen kun-yuan qiu Department of Polymer Science and Engineering, College of Chemistry, Peking University, Beijing 100871, China 北京大学北京

'Living'/controlled radical polymerization of ethyl methacrylate (EMA) was carried out with a 2,2'-azobisisobutyronitrile (AIBN)/ferric chloride (FeCl_3)/triphenylphosphine (PPh_3) initiation system at 85℃. Thc numberaverage molecular weight (M_n) increases linearly with monomer conversion and the rate of polymerization is first order withrespect to monomer concentration. The M_w of PEMA ranges from 3900 to 17600 and the polydispersity indices are quitenarrow (1.09～1.22). The conversion can reach up to～100% and M_w of the polymers obtained is close to that designed. Thepolymerization mechanism belongs to the reverse atom transfer radical polymerization (ATRP). The polymer was end-functionalized by chlorine atom, which acts as a macroinitiator to proceed extension polymerization in the presence ofCuBr/bipy catalyst system via an ATRP process. The presence of ω-chlorine in the PEMA obtained was identified by ~1H-NMR spectrum.

关键词： 'Living'/controlled radical polymerization Reverse ATRP Ethyl methacrylate AIBN/FeCl_3/PPh_3 Bulk polymerization

SYNTHESIS AND CHARACTERIZATION OF STRUCTURALLY WELL-DEFINED POLYMER-INORGANIC HYBRID NANOPARTICLES VIA ATRP

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Chinese Journal of Polymer Science 2002年第3期20卷 261-267页

作者： Jie Bai Jie-bin Pang kun-yuan qiu Yen Wei Department of Polymer Science & Engineering College of Chemistry & Molecular Engineering Peking University Beijing 100871, China Department of Chemistry Drexel University Philadelphia, PA 19104 USA Department of Polymer Science & Engineering College of Chemistry & Molecular Engineering Peking University 北京 100871 Department of Chemistry Drexel University 美国 Philadelphia PA 19104

Atom transfer radical polymerization (ATRP) using cuprous chloride/2,2'-bipyridine (bipy) was applied to graft polymerization of styrene on the surface of silica nanoparticles to synthesize polymer-inorganic hybrid nanoparticles, 2-(4Chloromethylphenyl) ethyltriethoxysilane (CTES) was immobilized on the surface of silica nanoparticles through condensation reaction of the silanol groups on silica with triethoxysilane group of CTES. Then ATRP of St was initiated by this surface-modified silica nanoparticles bearing benzyl chloride groups, and formed PSt graft chains on the surface of silica nanoparticles. The thickness of the graft chains increased with reaction time. End group analysis confirmed the occurrence of ATRP. Thermal analysis indicated that thermal stabilization of these resulting hybrid nanoparticles also increases with polymerization conversion. The results above show that this 'grafting from' reaction could be used for the preparation of polymer-inorganic hybrid nanoparticles with controlled structure of the polymer's end groups.

关键词： atom transfer radical polymerization polymer-inorganic hybrid nanoparticles 2-(4-chloromethylphenyl)ethyltriethoxysilane surface-modification

SYNTHESIS OF HYBRID MESOPOROUS POLYSTYRENE-SILICA MATERIALS WITH NON-SURFACTANT CITRIC ACID AS TEMPLATE VIA SOL-GEL PROCESS

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Chinese Journal of Polymer Science 2002年第6期20卷 565-572页

作者： Jie Bai Jin-yu Zheng kun-yuan qiu Yen Wei Department of Polymer Science & Engineering College of Chemistry & Molecular Engineering, Peking University Beijing 100871, China Department of Chemistry, Drexel University, Philadelphia, PA 19104, USA Department of Polymer Science & Engineering College of Chemistry & Molecular Engineering Peking University 北京 100871 Department of Chemistry Drexel University Philadelphia PA 19104 美国

Hybrid mesoporous polystyrene-silica materials were successfully prepared through HCl-catalyzed sol-gel reactions of tetraethyl orthosilicate (TEOS) and triethoxysilyl-functionalized polystyrene obtained via atom transfer radical polymerization (ATRP) of styrene, in the presence of citric acid (CA) as non-surfactant template or pore-forming agent and followed by ethanol extraction to remove template molecules. The materials were characterized by infrared spectroscopy OR), N-2 adsorption-desorption measurements, powder X-ray diffraction (XRD), thermogravimetric analysis (TGA) and transmission electron microscopy (TEM). The results indicate that the materials prepared with 50 wt%-60 wt% template contents have average pore sizes of 2-3 nm and large surface areas (ca. 886 m(2)/g) as well as high pore volumes (ca. 0.53 cm(3)/g). The mesoporosity arises from interconnected channels and pores with disordered arrangements. The pore diameters and pore volumes increase as the template content is increased. The pore diameters show a little change upon heating at 200degreesC overnight. However, the materials do not have good hydrothermal stability.

关键词： atom transfer radical polymerization hybrid material mesoporous polystyrene silica

SYNTHESIS OF MESOPOROUS POLY(STYRENE-co-MALEIC ANHYDRIDE)/SILICA HYBRID MATERIALS VIA A NONSURFACTANT-TEMPLATED SOL-GEL PROCESS

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Chinese Journal of Polymer Science 2000年第5期18卷 469-472页

作者： Jie-bin Pang kun-yuan qiu Yen Wei Department of Polymer Science and Engineering, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China. Department of Chemistry, Drexel University, Philadelphia, Pennsylvania 19104, USA. 北京大学北京 Drexel University 美国

Mesoporous poly(styrene-co-maleic anhydride)/silica hybrid materials have been prepared. The synthesis was achieved by the HCl-catalyzed sol-gel reactions of tetraethyl orthosilicate (TEOS) and styrene-maleic anhydride copolymer in the presence of 3-aminopropyl triethoxysilane (APTES) as a coupling agent and citric acid as a nonsurfactant template or pore-forming agent, followed by ethanol extraction. Characterization results from nitrogen sorption isotherms and powder X-ray diffraction indicate that polymer-modified mesoporous materials with large specific surface areas (e.g. 900 m(2)/g) and pore volumes (e.g. 0.6 cm(3)/g) could be prepared. As the citric acid concentration is increased, the specific surface areas, pore volumes and pore diameters of the hybrid materials increase.

关键词： mesoporous hybrid material poly(styrene-co-maleic anhydride)/silica citric acid nonsurfactant template sol-gel process

TARTARIC ACID TEMPLATED SYNTHESIS OF MESOPOROUS Ti-INCORPORATED SILICA AND ITS CATALYTIC ACTIVITY FOR THE RING-OPENING POLYMERIZATION OF ε-CAPROLACTONE

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Chinese Journal of Polymer Science 2002年第4期20卷 361-368页

作者： Jie-bin Pang Chang-ming Dong kun-yuan qiu Yen Wei Department of Polymer Science and Engineering College of Chemistry and Molecular Engineering Peking University Beijing 100871, China Department of Chemistry Drexel University Philadelphia, Pennsylvania 19104, USA Department of Polymer Science and Engineering College of Chemistry and Molecular Engineering Peking University 北京 100871 Department of Chemistry Drexel University 美国 Pennsylvania

Ti-incorporated mesoporous silica materials with pore diameters of 3-4 nm have been prepared via the co-hydrolysis and co-condensation reactions, that is the sol-gel reactions, of titanium (IV) tetrabutoxide and tetraethylorthosilicate in the presence of tartaric acid as template, followed by extraction with ethanol to remove the templatemolecules. The materials were characterized in detail by Fourier transform infrared spectroscopy, nitrogen adsorption-desorption test, powder X-ray diffraction, transmission electron microscopy and X-ray energy dispersive spectroscopy. Theresults indicate that the Ti-containing silica materials have large specific surface areas (ca. 1200 m^2 g^(-1)) and pore volumes(ca. 0.900 cm^3 g^(-1)). The mesoporosity arises from disordered interconnecting channels or pores. The Ti-incorporated silicasexhibit catalytic activity for the ring-opening polymerization of ε-caprolactone, otherwise, the pure mesoporous silicamaterial shows no catalytic activity under the identical conditions.

关键词： Mesoporous material Ti-incorporated silica ε-Caprolactone Ring-opening polymerization Sol-gel reactions

SYNTHESIS AND BIOTECHNOLOGICAL APPLICATIONS OF VINYL POLYMERINORGANIC HYBRID AND MESOPOROUS MATERIALS

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Chinese Journal of Polymer Science 2000年第1期18卷 1-7页

作者： Yen Wei kun-yuan qiu Department of Chemistry, Drexel University, Philadelphia, Pennsylvania 19104, USA Department of Polymer Science and Engineering, Peking University, Beijing 100871, China Drexel University 美国北京大学高分子科学与工程系北京

We describe the sol-gel synthesis of a new family of organic-inorganic hybrid materials, in which various vinyl polymers are covalently bonded to and uniformly distributed in inorganic oxide matrices. The materials can be tailored to have both good toughness and hardness while maintaining excellent optical transparency. Doping the sol-gel metal oxides with optically active compounds such as D-glucose results in new optical rotatory composite materials. Removal of the dopant compounds from the composites affords mesoporous oxide materials; which represents a new, nonsurfactant-templated route to mesoporous molecular sieves. We have successfully immobilized a series of enzymes and other bioactive agents in mesoporous materials. Catalytical activities of the enzyme encapsulated in mesoporous materials were found to be much higher than those encapsulated in microporous materials.

关键词： vinyl polymer-inorganic hybrid materials mesoporous materials sol-gel process biotech-nological applications

A NOVEL PHOTO-INITIATING SYSTEM FOR ATOM TRANSFER RADICAL POLYMERIZATION OF STYRENE

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Chinese Journal of Polymer Science 2001年第5期19卷 441-445页

作者： Shu-hui Qin Dong-qi Qin kun-yuan qiu Department of Polymer Science and Engineering College of Chemistry and Molecular Engineering Peking University Beijing 100871, China 北京大学北京

A novel photo-induced initiating system, 2,2-dimethoxy-2-phenylacetophenone (DMPA)/ferric tri(NN-diethyldithiocarbamate) [Fe(DC)(3)], was developed and used for the atom transfer radical polymerization (ATRP) of styrene in toluene. The polymerization proceeds with DMPA as photo-initiator, Fe(DC)(3) as catalyst and DC as a reversible transfer group, while the halogen and ligands are free. Well-defined PSt was prepared and the polymerization mechanism revealed by end group analysis belongs to a reverse ATRP. Block copolymer was prepared by using thus obtained PSt as macroinitiator and Fe(DC)(2) as catalyst under UV light irradiation via a conventional ATRP process.

关键词： photo atom transfer radical polymerization living radical polymerization well-defined polystyrene block copolymer

Dating Kimberlite Using Apatite U-Pb Geochronology: A Case Study from Diamond-Bearing Dikes in South China

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Journal of Earth Science 2024年第3期35卷 1059-1062页

作者： Jiawei Zhang Huan Wang Defeng He Yuhua Zhu kun Wang yuan qiu Guizhou Geological Survey Bureau of Geology and Mineral Exploration and Development of Guizhou ProvinceGuiyang 550081China College of Resources and Environmental Engineering Guizhou UniversityGuiyang 550025China Yanduzhongshi Geological Analysis Laboratory Ltd. Beijing 100080China State Key Laboratory of Ore Deposit Geochemistry Institute of GeochemistryChinese Academy of SciencesGuiyang 550081China

Kimberlite,one of the deepest known magmatic rocks on Earth,offers valuable glimpses into the deep mantle composition(Woodhead et al.,2019),craton structure(Gardiner et al.,2020),global geodynamic variation(Tappe et al.,2018),and diamond formation(Giuliani et al.,2023).The accurate determination of the emplacement of this special rock is crucial for revealing such ***,dating kimberlite is challenging due to its silica-poor,volatile-rich,strongly altered,and hybrid nature(Mitchell et al.,2019).Zircon is unsuitable for dating kimberlite and related rocks due to its preference for crystallizing in intermediate to felsic melts(Gervasoni et al.,2016)rather than silica-poor *** if present,zircon is prone to Pb loss through hydrothermal alteration(Zi et al.,2022)in a volatile-rich system like kimberlitic magmas.

关键词： dating magma alteration

Research on Credit Regulation Mechanism of E-commerce Platform Based on Evolutionary Game Theory

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Journal of Systems Science and Systems Engineering 2024年第3期33卷 330-359页

作者： Zeguo qiu Yuchen Yin Yao yuan Yunhao Chen School of Computer and Information Engineering Harbin University of CommerceHarbin150028China School of Management Harbin University of CommerceHarbin150028China

In the growing e-commerce industry,the problem of malicious business operations has become increasingly prominent,exposing many problems such as weak supervision of e-commerce platforms and no way for consumers to *** order to solve the problems of counterfeit and shoddy products on e-commerce platforms and promote the sustainable development of the e-commerce industry in China,this paper constructs a three-party evolutionary game model of e-commerce platforms,merchants,and consumers,investigates the influence of each influencing factor on each party’s strategy choice,and provides targeted suggestions to e-commerce platforms based on relevant ***,the impact of several important parameters on the equilibrium solution is discussed through sensitivity *** results show that:1)the smaller the cost difference between active and negative regulation,the more the e-commerce platform tends to active regulation strategy,but increasing fines for dishonest merchants and consumer complaints have little impact on the e-commerce platform;2)increasing consumer compensation,creating an honest business environment,and reducing the cost of honest business all help companies tend to operate in good faith;3)the only factor that affects the tendency of consumer complaint strategies is the cost of *** loss suffered by silence and the compensation given to consumers have little effect on consumers’tendency to complain *** results can provide theoretical guidance for participants to make useful strategic decisions in the e-commerce market.

关键词： Evolutionary game e-commerce data simulation