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| 1 | Synthesis of core-shell acrylic-polyurethane hybrid latex as binder of aqueous pigment inks for digital inkjet printing | Jingfang Zhang a,Xuefeng Li a,Xinhao Shi a,Mei Hua a,Xingping Zhou b,Xiaqin Wang a,a State Key Laboratory for Modification of Chemical Fibers and Polymer Materials,Donghua University,Shanghai 201620,China b College of Chemical Engineering and Biotechnology,Donghua University,Shanghai 201620,China | 2012 | Progress in Natural Science:Materials International2012，22，1： | 31 |
| 2 | Stimulus-responsive polymeric nanoparticles for biomedical applications显示文摘Polymeric nanoparticles with unique properties are regarded as the most promising materials for biomedical applications including drug delivery and in vitro/in vivo imaging.Among them,stimulus-responsive polymeric nanoparticles,usually termed as 'intelligent' nanoparticles,could undergo structure,shape,and property changes after being exposed to external signals including pH,temperature,magnetic field,and light,which could be used to modulate the macroscopical behavior of the nanoparticles.This paper reviews the recent progress in stimulus-responsive nanoparticles used for drug delivery and in vitro/in vivo imaging,with an emphasis on double/multiple stimulus-responsive systems and their biomedical applications. | LI YongYong1,2,DONG HaiQing1,2,WANG Kang1,SHI DongLu 2,ZHANG XianZheng1 & ZHUO RenXi1 1Key Laboratory of Biomedical Polymers,Ministry of Education Department of Chemistry,Wuhan University,Wuhan 430072,China 2Institute for Advanced Materials and Nano Biomedicine(iNANO),Tongji University,Shanghai 200092,China | 2010 | Science China Chemistry2010，53，3： | 11 |
| 3 | Syntheses of amphiphilic biodegradable copolymers of poly(ethyl ethylene phosphate) and poly(3-hydroxybutyrate) for drug delivery显示文摘Biodegradable and amphiphilic triblock copolymers poly(ethyl ethylene phosphate)-poly(3-hydroxybutyrate)-poly(ethyl ethylene phosphate) (PEEP-b-PHB-b-PEEP) have been successfully synthesized through ring-opening polymerization. The structures are confirmed by gel permeation chromatography and NMR analyses. Crystallization investigated by X-ray diffraction reveals that the block copolymer with higher content of poly(ethyl ethylene phosphate) (PEEP) is more amorphous, showing decreased crystallizability. The obtained copolymers self-assemble into biodegradable nanoparticles with a coreshell micellar structure in aqueous solution, verified by the probe-based fluorescence measurements and transmission electronic microscopy (TEM) observation. The hydrophobic poly(3-hydroxybutyrate) (PHB) block serves as the core of the micelles and the micelles are stabilized by the hydrophilic PEEP block. The size and size distribution are related to the compositions of the copolymers. Paclitaxel (PTX) has been encapsulated into the micelles as a model drug and a sustained drug release from the micelles is observed. MTT assay also demonstrates that the block copolymers are biocompatible, rendering these copolymers attractive for drug delivery. | CHENG Jing1 & WANG Jun2 1 Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei 230026, China 2 Hefei National Laboratory for Physical Sciences at Microscale, School of Life Sciences, University of Science and Technology of China, Hefei 230027, China | 2009 | Science China Chemistry2009，52，7： | 10 |
| 4 | Synthesis of Fe_3O_4@SiO_2@polymer nanoparticles for controlled drug release显示文摘Novel multifunctional nanoparticles containing a magnetic Fe3O4@SiO2 sphere and a biocompatible block copolymer poly(ethylene glycol)-b-poly(aspartate)(PEG-b-PAsp) were prepared.The silica coated on the superparamagnetic core was able to achieve a magnetic dispersivity,as well as to protect Fe3O4 against oxidation and acid corrosion.The PAsp block was grafted to the surface of Fe3O4@SiO2 nanoparticles by amido bonds,and the PEG block formed the outermost shell.The anticancer agent doxorubicin(DOX) was loaded into the hybrid nanoparticles via an electrostatic interaction between DOX and PAsp.The release rate of DOX could be adjusted by the pH value. | WU ChengLin,HE Huan,GAO HongJun,LIU Gan,MA RuJiang,AN YingLi & SHI LinQi Key Laboratory of Functional Polymer Materials,Ministry of Education Institute of Polymer Chemistry,Nankai University,Tianjin 300071,China | 2010 | Science China Chemistry2010，53，3： | 9 |
| 5 | Preparation of nano-sized Bi_2Te_3 thermoelectric material powders by cryogenic grinding | Xiaozong Chen a, Leifeng Liu b, Yuan Dong a, Lianjun Wang a, Lidong Chen c, Wan Jiang a, a State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Donghua University, 2999 people of North Road, Shanghai 201620, PR China b Department of Materials and Environmental Chemistry, Stockholm University, SE-106 91 Stockholm, Sweden c Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Dingxi Road, Shanghai 200050, PR China | 2012 | Progress in Natural Science:Materials International2012，22，3： | 8 |
| 6 | Microwave-assisted Polymerization of D,L-Lactide with Stannous Octanoate as Catalyst显示文摘Poly (lactic acid) (PLA) was synthesized by microwave-assisted ring-opening poly- merization of D, L-lactide with stannous octanoate (SnOct2) as catalyst. Its weight-average molar mass (Mw) ranged from 39000 to 67000 and the polydispersity index from 1.3 to 1.7. The polymerization rate was much faster than that of the conventional thermal polymerization. A degradation of newly formed PLA in reaction mixture by microwave irradiation was observed. | Li Jian LIU* Chao ZHANG, Li Qiong LIAO, Xu Li WANG, Ren Xi ZHUO Department of Polymer Science, College of Chemistry and Molecular Science, Wuhan University The Research Laboratory of SEDC of Biomedical Polymer Materials at Wuhan University, Wuhan 430072 | 2001 | Chinese Chemical Letters2001，12，8： | 7 |
| 7 | A pH-and temperature-sensitive macrocyclic graft copolymer composed of PEO ring and multi-poly(2-(dimethylamino) ethyl methacrylate) lateral chains显示文摘A novel method for the synthesis of macrocyclic graft copolymers was developed through combination of anionic ring-opening polymerization (AROP) and atom transfer radical polymerization (ATRP).A linear α,ω-dihydroxyl poly(ethylene oxide) with pendant acetal protected hydroxyl groups (l-poly(EO-co-EEGE)) was prepared first by the anionic copolymerization of ethylene oxide (EO) and ethoxyethyl glycidyl ether (EEGE).Then l-poly(EO-co-EEGE) was cyclized.The crude cyclized product containing the linear byproduct was hydrolyzed and purified by being treated with α-CD.The pure cyclic copolymer [c-poly(EO-co-Gly)] was esterified by reaction with 2-bromoisobutyryl bromide,and then used as ATRP macroinitiators to initiate polymerization of 2-(dimethylamino) ethyl methacrylate (DMAEMA),and a series of pH-and temperature-sensitive macrocyclic graft copolymers composed of a hydrophilic PEO as the ring and PDMAEMA as side chains (c-PEO-g-PDMAEMA) were obtained.The behavior of pH-and temperature-sensitive macrocyclic copolymers was studied in aqueous solution by fluorescence and dynamic light scattering (DLS).The critical micellization pH values of macrocyclic graft copolymers and their corresponding linear graft copolymers (l-PEO-g-PDMAEMA) were measured.Under the same conditions,the cyclic graft copolymer with the shorter side chains gave the higher critical micellization pH value.The c-PEO-g-PDMAEMA showed the lower critical micellization pH value than the corresponding l-PEO-g-PDMAEMA.The average hydrodynamic diameters (Dh) of the micelles were measured by DLS with the variation of the aqueous solution pH value and temperature. | PANG XinChang,JING RongKuan,PAN MuGang & HUANG JunLian Key Laboratory of Molecular Engineering of Polymers,Ministry of Education Department of Macromolecular Science,Fudan University,Shanghai 200433,China | 2010 | Science China Chemistry2010，53，8： | 6 |
| 8 | SYNTHESIS OF MESOPOROUS POLY(STYRENE-co-MALEIC ANHYDRIDE)/SILICA HYBRID MATERIALS VIA A NONSURFACTANT-TEMPLATED SOL-GEL PROCESS显示文摘Mesoporous poly (styrene-co-maleic anhydride)/silica hybrid materials have been prepared. The synthesis wasachieved by the HCl-catalyzed sol-gel reactions of tetraethyl orthosilicate (TEOS) and styrene-maleic anhydride copolymerin the presence of 3-aminopropyl triethoxysilane (APTES) as a coupling agent and citric acid as a nonsurfactant template orpore-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) andpore volumes (e.g. 0.6 cm^3/g) could be prepared. As the citric acid concentration is increased, the specific surface areas, porevolumes and pore diameters of the hybrid materials increase. | 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. | 2000 | Chinese Journal of Polymer Science2000，18，5： | 6 |
| 9 | A NEW METHOD TO PREPARE CHITOSAN MEMBRANE AS A BIOMEDICAL MATERIAL显示文摘This paper reports a new method to prepare chitosan membrane which could be used as a biomedical material.Addition of a fixation agent composed of alcohol, glycerol and potassium hydroxide can accelerate the sol-gel transformation process and hence shorten the preparation period. The present method takes about 6 h to get a flexible membrane with fine appearance. The physical and biological properties of the membrane were also investigated and compared with the membrane prepared by conventional method. | Qiao-ling Hu Zheng-ping Fang Ying Zhao Cheng-wei Xu Institute of Polymer Composites Zhejiang University Hangzhou 310027, China | 2001 | Chinese Journal of Polymer Science2001，19，5： | 6 |
| 10 | Synthesis of Nanoscale Shell-core Titania Coated Silica Particles in the Presence of Polyether Polyamine and the Phase Transition显示文摘The nanoscale titania coated silica was prepared via a two-step precipitating approach, where the nanoscale silica nuclei were first prepared by passing an aqueous solution of sodium silicate through an ion-exchange resin bed, then coated with the precipitation from hydrolyzed butyl titanate in an ethanol-hexane mixture at a low pH value in the presence of poly(ethylene oxide) polyamine salt(PPA) at a high temperature of 90 ℃. In the second-step precipitating process, the spontaneously precipitated titania shell on the silica nuclei was stabilized in the suspension solution with the help of the adsorption of PPA on the particles. A possible precipitating mechanism was suggested. Furthermore, the amorphous titania shell could undergo crystallization from the amorphous to the anatase structure at a high temperature of 650 ℃, and a further phase transition from the anatase to the rutile structure in the different sintering processes at a rising temperature of 750 ℃. | HUA Feng-jun 1, SUN Jun 2, HONG Ke 2, GAO Lian 1 and YANG Yu-liang 1** 1. Key Laboratory of Molecular Engineering of Polymer, Fudan University, Shanghai 200433, P. R. China 2. State Key Laboratory of High Performance Ceramics and Superfine Micros | 2002 | Chemical Research in Chinese Universities2002，18，1： | 6 |
| 11 | Synthesis and characterization of a strong-fluorescent Eu-containing hydrotalcite-like compound显示文摘A novel strong-fluorescent Eu-containing hydrotalcite-like compound (Eu-HTlc) was synthesized using the coprecipitation method,in which aluminum(III) was partially substituted by Europium (III) in the hydrotalcite-like layers,and thenoyltrifluoroacetone,1,10-phenanthroline were dispersed into the anions in the interlayer region.The sample was characterized by XRD,XPS,FT-IR,ICP,TG-DSC,TEM and fluorescence spectra,and its composition and structure were determined.The results indicated that the sample exhibited a characteristic red light (614 nm).The fluorescent lifetime and fluorescence quantum yield of Eu-HTlc were measured to be respectively 893 -s and 66.44%,higher than those of Eu(III)-thenoyltrifluoroacetone1,10-phenanthroline complex [Eu(TTA)3phen].The result of TG-DSC measurement showed the enhanced thermal stability of Eu-HTlc compared with that of MgAl-LDHs and Eu(TTA)3phen.With excellent photoluminescent property and thermal stability,low contents of rare earth ions and ligands,the Eu-HTlc may become one of the novel fluorescent materials with potential applications. | CHEN Hong & ZHANG WenGong Institute of Polymer Science,College of Chemistry and Materials Science,Fujian Normal University,Fuzhou 350007,China | 2010 | Science China Chemistry2010，53，6： | 5 |
| 12 | Encapsulation of inorganic particles by dispersion polymerization through ultrasonic irradiation显示文摘The nano-silica/polystyrene composite particles were prepared and characterized according to the following steps. First, the nano-silica particles were pretreated with surfactants under ultrasonic field. Second, the dispersion polymerization of styrene in a water/ethanol (1/6, weight ratio) medium, with poly(N-vinyl pyrrolidone) (PVP) as stabilizer and 2,2’-azobisizobu- tyronitrile (AIBN) as initiator in the presence of nano-silica particles was initiated with N2 purging through ultrasonic irradiation by taking its advantages of multieffect, i.e. dispersion, crushing, activation, and initiation. Finally, the polymerization kinetics characteristics were studied, and the encapsulation of composite particles was investigated with optical microscope, SEM, TEM, FTIR, X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). | ZHANG Kai1,2, FU Qiang1, HUANG Yuhong2 & ZHOU Dehui2 1. College of Polymer Science and Engineering, Sichuan University, Chengdu 610065, China 2. Institute of Structure Mechanics, China Academy of Engineering Physics, Mianyang 621900, China | 2005 | Science China Chemistry2005，48，6： | 5 |
| 13 | Interfacial behaviors of PMMA-PEO block copolymers at the air/water interface显示文摘Diblock copolymer of PMMA291-b-PEO114 and triblock copolymer of PMMA120-b- PEO227-b-PMMA120 were synthesized and their interfacial properties at the air-water interface were investigated, where both blocks of polyethylene oxide (PEO) and poly(methyl methacrylate) (PMMA) are surface active but the former is soluble in water while the latter is not. Both the block copolymers could form monolayers with two obvious transition regions. The first transition point is around 10 mN/m, which could be assigned to the pancake-brush change of the PEO chains. The other is around 18 mN/m, which could be ascribed to the condensed packing of PMMA. The surface morphological changes during the compression of the Langmuir monolayers are inves-tigated by using the AFM and SEM methods for the films deposited at different surface pressure or molecular areas. At a lower surface pressure, a typical morphology of PEO-con- taining lipopolymers is observed. Upon compression, sphere-dominant morphologies were observed. While the diblock copolymer is easy to folding, the triblock copolymer is in favor of formation of circular domains through vesiculation. | CHENG Caixia1, JIAO Tifeng2, TANG Rupei1, LIU Minghua2 & XI Fu1 1. State Key Laboratory of Polymer Physics and Chemistry, Joint Laboratory of Polymer Science and Materials, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100080, China 2. CAS Key Laboratory of Colloid and Interface Science, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100080, China | 2005 | Science China Chemistry2005，48，6： | 5 |
| 14 | Miktoarms hyperbranched polymer brushes:One-step fast synthesis by parallel click chemistry and hierarchical self-assembly显示文摘Spherical molecular brushes with amphiphilic heteroarms were facilely synthesized by grafting the arms of hydrophobic 2-azidoethyle palmitate and hydrophilic monoazide-terminated poly(ethylene glycol) onto the core of alkyne-modified hyperbranched polyglycerol (HPG) with high molecular weight (Mn=122 kDa) via one-pot parallel click chemistry.The parallel click grafting strategy was demonstrated to be highly efficient (~100%),very fast (~ 2 h) and well controllable to the amphilicity of molecular brushes.Through adjusting the feeding ratio of hydrophobic and hydrophilic arms,a series of brushes with different arm ratios were readily obtained.The resulting miktoarms hyperbranched polymer brushes (HPG-g-C16/PEG350) were characterized by hydrogen-nuclear magnetic resonance (1H NMR),Fourier transform infrared (FT-IR) spectroscopy,gel permeation chromatography (GPC),and differential scanning calorimetry (DSC) measurements.The spherical molecular brushes showed high molecular weights up to 230 kDa,and thus could be visualized by atomic force microscopy (AFM).AFM and dynamic laser light scattering (DLS) were employed to investigate the self-assembly properties of amphiphilic molecular brushes with closed proportion of hydrophobic and hydrophilic arms.The brushes could self-assemble hierarchically into spherical micelles,and network-like fibre structures,and again spherical micelles by addition of n-hexane into the dichloromethane or chloroform solution of brushes.In addition,this kind of miktoarms polymer brush also showed the ability of dye loading via host-guest encapsulation,which promises the potential application of spherical molecular brushes in supramolecular chemistry. | HAN Yi & GAO Chao MOE Key Laboratory of Macromolecular Synthesis and Functionalization Department of Polymer Science and Engineering,Zhejiang University,Hangzhou 310027,China | 2010 | Science China Chemistry2010，53，12： | 5 |
| 15 | Electroluminescence and photoluminescence of dioctylfluorene and 4,7-dithien-2-yl-2,1,3-benzothiadiazole copolymers显示文摘Dioctylfluorene (DOF) and 4,7-dithien-2-yl-2,1,3-benzothiadiazole (DBT) copolymers synthesized in our lab with different compositions of DBT (1%, 5%, 15% and 25%) were utilized to fabricate bilayered light emitting diodes. External quantum efficiency (QE) of the diode fabricated from the copolymer with 15% DBT content reaches 1.4% (ph/el), over 1.0 cd/A in luminance efficiency at the driving voltage of 4.2 V. The highest luminance can reach 3780 cd/m2 at 8.2 V. Devices emit a saturated red light centered at 675 nm with chromaticity coordinate changed from x=0.66, y=0.32 for PDOF-DBT1 (1% DBT) to x=0.70, y= 0.28 for PDOF-DBT25 (25% DBT). | PENG Junbiao, XU Yishe, HOU Qiong, NIU Yuhua, RUAN Wenying & CAO YongInstitute of Polymer Optoelectronic Materials & Devices, South China University of Technology, Guangzhou 510640, China Department of Applied Physics, South China University of Technology | 2002 | Chinese Science Bulletin2002，47，20： | 5 |
| 16 | STRESS-INDUCED CRYSTALLIZATION OF POLYURETHANE/MONTMORILLONITE NANOCOMPOSITE显示文摘Exfoliated polyurethane/montmorillonite nanocomposites with both high elongation at break and high tensile strength were studied by dynamic-infrared spectroscopy (dynamic-IR). The results show that crystallization induced by additional stress is impeded by the nano-layered organo montmorillonite. | Xin-hua Dai Xiang-dong Luo Qun Gu Xiao-li Zhang De-yan Shen Liang-he Shi Jian Xu State Key Laboratory of Polymer Physics and Chemiscy Center for Molecular Science, Institute of Chemistry,Chinese Academy of Sciences, Beijing 100080, China | 2002 | Chinese Journal of Polymer Science2002，20，5： | 4 |
| 17 | Semibatch Emulsifier-free Emulsion Copolymerization of Methyl Methacrylate and n-Butyl Acrylate in the Presence of 2-Hydroxyethyl Methacrylate显示文摘The sendbatch emulsifier-free emulsion copolymerization of methyl methacrylate (MMA) and n-butyl acrylate (BA) in the presence of 2-hydroxyethyl methacrylate (HEMA) initiated by K2S2O8 (PSP) was studied. The average palticle diameter increases with an increase of total solids content, HEMA content, PSP content, ionic strength of the system and monomer feed rate, and decreases with the monomer feed ratio from 3/1 (MMA/BA mole.) to 1/3. The stability of this reaction system is improyed by adding HEMA as nonionic comonomer. The high so1ids content (50%) latex with monodisperse particle can be obtained using this process. | Tian Ying GUO Mou Dao SONG Qing Ye ZHOU Bang Hua ZHANG Jian Biao MA Bing Lin HE (The State key Laboratory of Functional Polymer Materials for Adsorption and Separation,Institute of Polymer Chendstry, Nankai University, Tianin, 300071) | 1998 | Chinese Chemical Letters1998，9，7： | 4 |
| 18 | Synthesis of Novel Poly(aryl ether amide)s Containing the Phthalazinone Moiety显示文摘Two novel heterocyclic diamine monomers: 1,2-dihydro-2-(4-aminophenyl)-4-[4-(4- amin- ophenoxy)phenyl](2H)phthalazin-l and 1,2-dihydro-2-(4-aminophenyl)-4-[4-(4- aminophenoxy)-3.5-dimethylpheny] (2H)phthalazin-1-one were successfully synthesized from readily available heterocyclic bisphenol-like monomers in two steps in high yield. A series of novel poly(aryl ether amide)s containing the phthalazinone moiety were successfully prepared by the direct polymerization of the novel diamines and aromatic dicarboxylic acids using triphenyl phosphite and pyridine as condensing agents. | Lin CHENG~1 Xi Gao JIAN~2 (~1Department of Materials Science & Engineering, Wuhan Institute of Chemical Technology. Wuhan 430074) (Department of Polymer Science & Materials. DaLian University of Technology. DaLian 1 16012) | 2000 | Chinese Chemical Letters2000，11，4： | 4 |
| 19 | Ring-opening Polymerization ofε-Caprolactone Using Lanthanide Tris(4-tert-butylphenolate)s as a Single-component Initiator显示文摘The ring-opening polymerization of ε-caprolactone (CL) initiated by novel singlelanthanide tris(4-tert-butylphenolate)s [Ln(OTBP)3] is reported. Single-component La(OTBP)3can effectively prepare polycaprolactone (PCL) with over 90% yield and viscosity averagemolecular weight about 60 × 103 under quite mild conditions: molar ratio of CL to initiator is 1000,60 ℃, 2 h in toluene. Mechanism study indicates that the monomer inserts into the growing chainvia the break of acyl-oxygen bond of CL. | Cui Ping YU, Li Fang ZHANG, Zhi Quan SHEN Institute of Polymer Science, Zhejiang University, Hangzhou 310027 | 2003 | Chinese Chemical Letters2003，14，10： | 4 |
| 20 | NUMERICAL SIMULATION OF MORPHOLOGY OF POLYMER CHAIN COILS IN COMPLEX FLOWS显示文摘A new coupled finite element formulation is proposed to calculate a conformation tensor model in two complex flows: a planar contraction flow and a planar flow around a symmetrically placed cylinder. The components of conformation tensor are first computed together with the velocity and pressure to describe the change of morphology of polymer chain coils in flow fields. Macroscopic quantities of viscoelastic flow are then calculated based on the conformation tensor. Comparisons between the numerical simulations and experiments for stress patterns and velocity profiles are carried out to prove the validity of the method. | Hong Zheng Wei Yu Chi-xing Zhou Department of Polymer Materials Science & Engineering,Shanghai Jiaotong University,Shanghai 200240,China | 2005 | Chinese Journal of Polymer Science2005，23，5： | 4 |
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