Loading...

Table of Content

    10 December 2015, Volume 36 Issue 12
    Content
    Cover and Content of Chemical Journal of Chinese Universities Vol.36 No.12(2015)
    2015, 36(12):  0-0. 
    Asbtract ( )   PDF (1418KB) ( )  
    Related Articles | Metrics
    Volume Contents of Chemical Journal of Chinese Universities to Vol.36(2015)
    2015, 36(12):  0-0. 
    Asbtract ( )   PDF (728KB) ( )  
    Related Articles | Metrics
    Articles: Inorganic Chemistry
    Optimized Synthesis and Characterization of Highly Ordered Mesoporous Al-SBA-15 with High Hydrothermal Stability
    XU Qian, DONG Zhaoyang, SHI Guoliang, PAN Dahai, YU Feng, CHEN Shuwei, LI Ruifeng
    2015, 36(12):  2355-2363.  doi:10.7503/cjcu20150543
    Asbtract ( )   HTML ( )   PDF (3900KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Highly ordered mesoporous Al-SBA-15 materials with high aluminum content and high hydrothermal stability were synthesized by one-step hydrothermal grafting approach under the weak acid medium produced only by the hydrolysis of inorganic aluminum salt. By selectively introducing inorganic aluminum salt in the synthesis system, and further optimizing hydrothermal treatment temperature and the introduced amount of inorganic aluminum salt, the hydrolysis of Al ion and the condensation of silicon hydroxyl(Si—OH) species within the mesoporous walls could be efficiently controlled to adjust the relative amount of Al—OH and Si—OH groups and their interaction. As a result, the ordered mesostructure of Al—SBA—15 could be assembled at the mesoscale and the coordination status/the acidic sites could be controlled at the atomic scale. The characteristic results by means of XRD, N2 adsorption, TEM, EDX, SEM, FTIR and NMR techniques showed that when aluminium nitrate was used as the aluminum precursor, and hydrothermal treatment temperature and initial molar ratio of silicate to aluminium were adjusted as 140 ℃ and 10, respectively, the synthesized sample exhibited highly ordered hexagonal mesostructure and extremely high hydrothermal stability. The highly ordered mesostructure can be maintained even after steam treatment at 800 ℃ for 2 h with only 18.82% and 16.67% decreases in the Brunauer-Emmett-Teller surface area and total pore volume, respectively. Moreover, the hydrothermal grafting process at 140 ℃ was advantageous for the homogeneous incorporation of Al into the silica mesoporous framework to form the Si—OH—Al bond, leading to the production of Brönsted and Lewis acid sites with relatively strong acidity on the mesoporous walls.

    Effects of Magnetic Field on the Morphology and Properties of BiFeO3 Synthesized by Hydrothermal Method
    SHI Xuanxuan, XIAO Ruijuan, WANG Zhen, ZHOU Jianping, BIAN Xiaobing
    2015, 36(12):  2364-2371.  doi:10.7503/cjcu20150464
    Asbtract ( )   HTML ( )   PDF (8781KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    BiFeO3 powders were synthesized by hydrothermal method under different magnetic fields with KOH concentrations of 2—7 mol/L at 140—220 ℃ for 1—12 h, using Bi(NO3)3·5H2O and Fe(NO3)3·9H2O as reaction materials and KOH as the mineralizer. The external magnetic field expanded the experimental range of alkali concentration and reaction temperature for the synthesis of pure BiFeO3 phase. SEM images showed that the magnetic field effectively reduced the BiFeO3 particle size. The results of photocatalytic experiment showed that the photocatalytic activity of the BiFeO3 powders increased with decreasing particle size. The magnetization was increased and the intensity of A1-2 resonance mode in Raman spectra was enhanced for BiFeO3 prepared under mangetic field.

    Hydrothermal Synthesis, Characterization and Photocatalytic Activities of Nanosheets-assembled Bi12SiO20 Microcubes
    ZHANG Xiang, ZHANG Lei, ZOU Yue, HUANG Xinhua, PAN Chengling, HOU Changmin, XU Jiqing
    2015, 36(12):  2372-2379.  doi:10.7503/cjcu20150413
    Asbtract ( )   HTML ( )   PDF (6648KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Novel nanosheet-assembled Bi12SiO20 microcubes were prepared via a facile hydrothermal synthesis approach. The phase and morphology of the product were characterized by X-ray diffraction, energy dispersive spectrometry, selected area electron diffraction, X-ray photoelectron spectrometry, high resolution transmission electron microscopy and scanning electron microscopy. Experimental results indicated that as-prepared Bi12SiO20 sample was assembled by many nanosheets. Some influencing factors including reaction time, temperature and the presence of additives(e.g., polyacrylamide, sodium citrate and sodium hydroxide) were revealed to play crucial roles in the generation of Bi12SiO20 nanoarchitecture. Moreover, the photocatalytic experiments indicated that the as-prepared Bi12SiO20 product exhibited excellent photocatalytic activities and the degradation rate of RhB could reach to 97.5% under the irradiation of UV-Vis light.

    Synthesis, Structures and Photochemical Properties of Two New Cd(II) Metal-organic Frameworks Isolated from the Same Reaction System
    ZHAO Lun, ZHANG Min, SUN Erjun, WANG Xiaofeng, WANG Zichen
    2015, 36(12):  2380-2385.  doi:10.7503/cjcu20150471
    Asbtract ( )   HTML ( )   PDF (3914KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    The solvothermal reactions of Cd(NO3)2 with 4,4'-(phenylazanediyl)dibenzoic acid(H2L) and 1,4-bis(pyridin-4-ylmethl)piperazine(bpmp) gave rise to a mixture of colorless sheet-like crystals {[CdL(bpmp)(H2O)]·H2O·DMF}n(1) and yellowish bulk crystals {[Cd2L2(bpmp)2]·3H2O·2DMF}n(2), which were mechanically separated. Both compounds were structurally determined by single-crystal X-ray diffraction. Compounds 1 and 2 were also characterized by FTIR spectroscopy, elemental analyses, thermal analysis, and powder X-ray diffraction(PXRD). Compound 1 exhibits a 4-fold interpenetrating 3D framework with a {65·8} topology. Compound 2 consists of 1D [Cd2L2]n helical chains linked by bpmp ligands to form a 2D network with a {36·46·53} topology.

    Analytical Chemistry
    NUPACK Prediction Assisted of Toehold Induced Strand Displacement Reaction and Its Application in SNPs Genotyping by DNAzyme-catalyzed Microfluidic Chemiluminescence Detection
    WU Qiwang, SHEN Hong
    2015, 36(12):  2386-2393.  doi:10.7503/cjcu20150427
    Asbtract ( )   HTML ( )   PDF (3241KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Highly sensitive and selective method for single nucleotide polymorphisms(SNPs) genotyping is of great importance for early diagnosis and treatment of various diseases. By taking rs242557, an Alzheimer’s disease related gene fragment, as a target model, the impact of toehold length on strand displacement reaction was predicted by NUPACK software simulation in order to rationalize the design of duplex DNA probe for high genotyping efficiency. The G-rich DNA sequence was initially blocked in the duplex strand structure. With the addition of target gene fragment to trigger the blocked-domain dehybridization and the toehold-mediated strand displacement reaction, the DNAzyme was formed. Combined with microfluidic chemiluminescence detection, a novel SNP genotyping method had been developed, which was not only label-free, easy to design and exhibited high throughput ability, but also displayed a remarkable specificity to target rs242557 against single base mutation, achieving a discrimination factor of 56 and a detection limit of 1.7 nmol/L with just 2 μL of sample solution consumption.

    Molecular Interactions of 1-Hydroxypyrene with Catalase Revealed by Spectroscopic Methods Combined with Molecular Docking
    CHEN Linfeng, ZHANG Jing, ZHU Yaxian, ZHANG Yong
    2015, 36(12):  2394-2401.  doi:10.7503/cjcu20150367
    Asbtract ( )   HTML ( )   PDF (2920KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    The interactions between 1-hydroxypyrene(1-OHP) and catalase(CAT) were investigated by fluorescence, UV visible absorption(UV-Vis) spectra and molecular docking methods in aqueous solutions. The experimental results showed that the intrinsic fluorescence of CAT was quenched by the addition of 1-OHP through a static quenching mechanism. 1-OHP can bind with CAT to form 1:1 complex, with a binding constant of 2.96×105 L/mol at 290 K. The result of thermodynamic analysis indicated that hydrogen bonds and van der Waals’ force were the dominant intermolecular forces in stabilizing the complex. Based on the Förster’s non-radiation energy transfer theory, the binding distance between 1-OHP and CAT was determined to be 3.48 nm. The synchronous fluorescence and UV-Vis absorption spectral results showed that the formation of 1-OHP-CAT complex can induce some conformation changes of CAT. And in the presence of high concentrations of 1-OHP, the CAT activity can be inhibited obviously. Molecular docking was further employed to seek the optimum binding site of 1-OHP in CAT, and get the detailed binding information, which is identical to the experiment results. This work contributes to understand the interaction mechanism between 1-OHP and CAT at the molecular level, and provides important insights to study the toxicity mechanism of PAHs and their metabolites on antioxidant enzyme system in organisms.

    Preparation of Quercetin Imprinted Polymer by Living Radical Polymerization and Its Application in the Composition Analysis of Zukamu Granules for Uighur Medicine
    TURSON Mamat, DAWUT Gulbahar, EMIN Risalat, CHU Ganghui, JELIL Mahmutjan, TURHON Muhetar
    2015, 36(12):  2402-2408.  doi:10.7503/cjcu20150357
    Asbtract ( )   HTML ( )   PDF (3736KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Quercetin imprinted polymer was synthesized by a reversible addition-fragmentation chain transfer(RAFT) polymerization method, combining molecular imprinting with living radical polymerization techniques, usingthe dibenzyltrithiocarbonate(DBTTC) as reversible RAFT reagent, quercetin as the imprinted compound, and the methacrylic acid(MAA), acrylamide(AM), acrylic acid(AA), 4-vinylpyridine(4-VP) and 2-vinylpyridine(2-VP) as functional monomers, ethyleneglycoldim ethacrylate(EDMA) as cross-linker and 2,2-azob isisobuty ronitrile(AIBN) as initiator.The preparation of molecular imprinted polymers(MIPs) were conducted under different experimental conditions, and the structures of the MIPs were characterized by nitrogen adsorption and scanning electron microscopy, respectively. The identify ability and separation efficiency of MIPs for quercetin were evaluated by high performance liquid chromatography(HPLC). The relationship among the polymerization conditions, structure of polymer and separation efficiency was studied, and the synthetic method and characteristics of MIPs prepared by living radical polymerization were also explored. The quercetin was separated and enriched in Zukamu Granules for Uighur medicine, using synthesized MIPs as stationary phase. The results showed that the MIPs synthesized by living radical polymerization method exhibited a better morphology, and a good adsorption efficiency for the target molecule.

    Organic Chemistry
    Synthesis and Properties of Triphenylamine-containing Asymmetrical Perylene Diimides
    KONG Lushi, TIAN Guofeng, LI Feng, QI Shengli, WU Dezhen
    2015, 36(12):  2409-2414.  doi:10.7503/cjcu20150549
    Asbtract ( )   HTML ( )   PDF (2105KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Two asymmetrical perylene diimides with triphenylamine structure, N-(2-ethylhexyl)-N'-(4-triphenylamine)-3, 4, 9, 10-perylene diimide(PDI-ATPA) and 4, 4', 4''-tri[N-(2-ethylhexyl)-3, 4, 9, 10-perylene diimide]-triphenylamine(PDI-TATPA), were designed and synthesized, using branched alkyl chain substituted asymmetrical perylene monoanhydride monoimide(AsPDA-Ⅰ) as the electron-accepting species and different functional triphenylamines, 4-aminotriphenylamine(ATPA) and 4, 4', 4''-triaminotriphenylamine(TATPA), as the electron-donating moieties, respectively. The chemical structures were characterized by proton nuclear magnetic resonance(1H NMR), Infrared(IR) spectra and elemental analysis. The optical properties and aggregation behavior in solution were investigated by UV-Vis absorption and fluorescence emission spectra. Besides, molecular simulations were carried out to elucidate the molecular orbitals, energy levels and dipole moments of two asymmetrical perylene diimides. The results demonstrated that introducing the triphenylamine structure at the imide nitrogen of perylene diimide not only broadens the photo absorption region of perylene diimide but also has no effect on the absorption properties of the perylene core because of nodes in the highes occupied molecular orbital(HOMO) and lowest unoccupied molecular orbital(LUMO) at the imide nitrogen. Photoinduced electron transfer(PET) process take place from the eletron-donating moieties-ATPA and TATPA to the electron-accepting unit-perylene core, which has been confirmed by molecular simulations and lead to the fluorescence quenching. PDI-TATPA showed a star-shaped structure with highly regularity, which has been proven by the simulation data of dipole moment and has caused the self-assembly behavior easily occur in solution. Due to the self-assembly behavior, there are some differences between the UV-Vis spectra of PDI-ATPA and that of PDI-TATPA.

    Synthesis and Fungicidal Activities of Biaryl Methanone O-Benzyl Oximes
    LI Xiuyun, WAN Chuan, DU Shijie, LI Hong, YUAN Huizhu, JIANG Jiazhen, XIAO Yumei, QIN Zhaohai
    2015, 36(12):  2415-2420.  doi:10.7503/cjcu20150508
    Asbtract ( )   HTML ( )   PDF (1215KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    To discover new strobilurin analogs with high pesticidal activity, 11 novel methoxy acrylates bearing biaryl methanone oxime ether moieties were synthesized from aroyl pyridines, and characterized by 1H and 13C NMR and HRMS. In vitro fungicidal evaluation indicated that all of the target compounds exhibited excellent activities against tested seven phytopathogenic fungi, and compounds 5d and 5g displayed comparable overall activities to azoxystrobin and trifloxystrobin. Some of the target compounds also exhibited excellent in vivo control effects at 400 mg/L, for example, compound 5h could 100% control wheat powdery mildew and cucumber anthracnose. Furthermore, at 25 mg/L, these compounds, including control agents, completely inhibited spores germination of rice blast, but no effect at all for cucumber gray mold. These results suggested that this class of compounds might deserve to be developed as new potential agricultural fungicides.

    Bridged Di-py-cavitand Compounds as Molecular Switch
    XU Hai, ZHAO Siqi, REN Yang, CAI Jianfeng, WANG Xiang, LIN Yulin
    2015, 36(12):  2421-2426.  doi:10.7503/cjcu20150445
    Asbtract ( )   HTML ( )   PDF (2663KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Two kinds of di-py-cavitand compounds with different arm lengths were synthesized using molecular switch which configurations are variable-class calixarene cavities(Cavitand) as the parent compounds. In the neutral state of room temperature, the two kinds of di-py-cavitand compounds can detect intramolecular exciplex fluorescence and the compounds with short arm is obviously more stronger than the long arm one in the fluorescence intensity. However, intramolecular exciplex fluorescence disappears after acidification by trifluoroacetic acid and appears again when continuing to add alkali so as to neutralize to neutral state. The process of fluorescence appearing-disappearing-appearing powerfully verified that the process of closing-opening-closing of the molecular configuration of cavitand parent compounds can efficiently control intramolecular exciplex fluorescence’s opening and closing processes. In addition, the molecular configurations of di-py-cavitand compounds in theory with different arm length were simulated through Gaussian calculation module, finding that two pyrene groups of di-py-cavitand compound with long arm were less overlaped when the cavitand parent configuration was in the closing state, which is the key cause of the corresponding weak intramolecular exciplex fluorescence intensity.

    Synthesis and Anti-tumor Activity of Novel Amino Acid Glyceroglycolipid
    AN Dong, YE Zhiwen, ZHOU Mi
    2015, 36(12):  2427-2434.  doi:10.7503/cjcu2015405
    Asbtract ( )   HTML ( )   PDF (1574KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Glyceroglycolipids have been identified as one of the most important anticancer drug. In this work, novel amino acid glyceroglycolipids were synthesized through the esterification of glycosylglycerol and N-acyl amino acid and characterized by means of 1H NMR and ESI-MS. The anti-tumor activities against human breast cancer cell line, human liver cancer cell line and chronic myeloid leukemia cell line in vitro were tested by MTT method. The preliminary results demonstrated that compounds 27(IC50=3.53, 4.71, 4.13 μmol/L), 28(IC50=4.35, 4.57, 5.79 μmol/L), 31(IC50=3.91, 3.73, 4.54 μmol/L) and 32(IC50=5.17, 5.52, 5.93 μmol/L) exhibited significant anti-tumor activities. The preliminary studies on the structure-activity relationship showed that when the acyl was decanoyl or lauroyl, good activity was exhibited in all the eight different kinds of glycosyl diacylglycerols. The preliminary prediction of this type of compound had certain inhibitory effect on the growth of tumor cells, they are non-toxic to normal cells. Such novel amino acid glyceroglycolipids as antineoplastic drugs or excellent surfactants could be widely investigated in the future.

    Syntheses and Antitumor Activities of Phenylpiperazine Derivatives
    WANG Gang, HAN Leiqiang, FANG Hao
    2015, 36(12):  2435-2440.  doi:10.7503/cjcu20150397
    Asbtract ( )   HTML ( )   PDF (1702KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    The structure of phenylpiperazine as an important pharmacophore could generate wide pharmacological activities. In this work, a series of novel phenylpiperazine derivatives was designed, synthesized and their preliminary antiproliferative activities against tumor cell lines were evaluated using MTT assay. Results indicated that the most active target compound 4t had the substitution of benzenesulfonamides and benzofuran on N1 and N4 position of piperazine respectively. Furthermore, IC50 values of compound 4t against five tumor cell lines in vitro were determined. Compound 4t could inhibit the growth of some tumor cell lines and showed similar inhibitory activities against MDA-MB-231 tumor cell line(IC50=3.50 μmol/L) compared with Gossypol(IC50=1.40 μmol/L). These results provided useful information for designing new phenylpiperazine derivatives with higher antitumor activity.

    Unexpected Oxidation of α-Aryl-α-hydroxyketone(ester) with Perfluoroalkanosulfonyl Fluoride/Methyltriethoxysilane/Base System
    YAN Zhaohua, ZHAO Dongdong, HU Wei, TIAN Huan, LI Xiaosong, TIAN Weisheng
    2015, 36(12):  2441-2445.  doi:10.7503/cjcu20150276
    Asbtract ( )   HTML ( )   PDF (1299KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Aryl substituted 1,2-diketone(α-ketonic esters) have been widely used as important intermediates for syntheses of ligands, bioactive molecules and functional materials. As a class of excellent hydroxyl-activating reagent, the application of perfluoroalkanosulfonyl fluoride in organic synthesis has been intensively investigated in the past decades. In this work, oxidation of α-aryl-α-hydroxyketone(ester) with perfluoroalkanosulfonyl fluoride/methyltriethoxysilane/base system in CH2Cl2 at room temperature was further studied and the corresponding 1,2-diketone(ketonic ester) was generated in moderate to good yields. Perfluoroalkanosulfonyl fluoride used is n-perfluorobutanosulfonyl fluoride or n-perfluorooctanosulfonyl fluoride; base used is 1,8-diazabicyclo[5.4.0]undec-7-ene(DBU). A reasonable reaction mechanism was proposed to explain the results. A novel method for the preparation of aryl substituted 1,2-diketone(ketonic ester) was developed. The application scope of perfluoroalkanosulfonyl fluoride in organic synthesis was broadened.

    Preparation and Biological Evaluation of 99mTc-labeled Pteroyl-lys Derivatives
    YU Qian, HE Yingfang, CHEN Yuan, YANG Wenjiang, ZHANG Chun, LU Jie
    2015, 36(12):  2446-2453.  doi:10.7503/cjcu20150388
    Asbtract ( )   HTML ( )   PDF (2693KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Two 99mTc labeled complexes, 99mTc(HYNIC-penta-lys-Pteroyl)(Tricine/TPPTS) and 99mTc-(HYNIC-Gly-Gly-lys-Pteroyl)(Tricine/TPPTS), were prepared based on the structure of Pteroyl-lys. Both two complexes exhibited high receptor specific binding and extended retention in KB human epidermoid carcinoma cells. The tumor uptake values of 99mTc(HYNIC-penta-lys-Pteroyl)(Tricine/TPPTS) and 99mTc(HYNIC-Gly-Gly-lys-Pteroyl)(Tricine/TPPTS) were (8.55±2.78)%ID/g and (9.77±1.54)%ID/g at 1 h postinjection, respectively. Flank KB tumors were clearly visualized with 99mTc(HYNIC-penta-lys-Pteroyl)(Tricine/TPPTS) and 99mTc(HYNIC-Gly-Gly-lys-Pteroyl)(Tricine/TPPTS) by Micro-SPECT/CT images at 2 h postinjection. High receptor-specific tumor uptakes coupled with fast non-target tissues clearance demonstrated the feasibility of using 99mTc-labeled Pteroyl-lys derivatives as novel imaging probes for FR-positive tumors detection.

    Cloning and Application of a New Acylaminoacyl Peptidase from Bacillus subtilis 168 for Aldol Reaction
    YU Xiaoxiao, WANG Qi, ZHOU Ye, GAO Renjun, WANG Yingwu
    2015, 36(12):  2454-2460.  doi:10.7503/cjcu20150358
    Asbtract ( )   HTML ( )   PDF (3465KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Acylaminoacyl peptidase has been named acyl-peptide releasing enzyme(AARE), catalyses the removal of an N-acylated amino acid from N-α-acylpeptides. In this research, a novel acyl-peptide releasing enzyme gene(BSU32230) from Bacillus subtilis 168 was cloned and expressed in Escherichia coli BLP DE3 codon plus to produce acyl-peptide releasing enzyme. The recombinant enzyme was purified in two steps: ammonium sulfate precipitation and Ni2+-column affinity chromatography. The optimum temperature and pH of enzyme were 50 ℃ and 8.0, respectively. The half-life of recombinant enzyme at 40 ℃ was 29 h, the enzyme was stable at pH range from 4 to 10. This report demonstrated the acylaminoacyl peptidase from Bacillus subtilis peptidase can catalyze aldol reaction and showed high enantioselectivity. The reaction provided optically active secondary alcohol with satisfying enantioselectivity(84.6% e.e.).

    Physical Chemistry
    Au(Ⅰ) Complexes as the Efficient Catalyst for Hydration of Alkynes at Room Temperature
    WU Gongde, WANG Xiaoli, ZHANG Liming, JIANG Taineng
    2015, 36(12):  2461-2467.  doi:10.7503/cjcu20150523
    Asbtract ( )   HTML ( )   PDF (2608KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    A series of (1,1'-biphenyl)-2-yldi(adamantan-1-yl) phosphine ligands was synthesized to prepare eight kinds of Au(Ⅰ) complexes. And their catalytic performances were investigated in the hydration of alkynes using methanol as solvent. At room temperature, it was found that Au(Ⅰ) complexes containing the group of 3'-(pyrrolidin-1-ylcarbonyl) showed the excellent catalytic performance in the hydration of alkynes with the catalyst loading of 0.1%―0.3%(molar fraction, base on alkynes). The reaction parameters were further optimized for spreading the applied scope of the catalysts. Therefore, a mild catalytic system with good applicability was explored for the hydration of terminal and internal alkynes using less dosage of catalyst.

    Fabrication and Performance of a Novel Visible Light-driven Fuel Cell Based on Photocatalytic Oxidation of Uric Acid by CdS Nanoparticles and Electrocatalytic Reduction of Oxygen by a Copper(Ⅱ) Complex
    LUO Jinyuan, CHEN Linlin, WANG Yi, LI Hong
    2015, 36(12):  2468-2474.  doi:10.7503/cjcu20150469
    Asbtract ( )   HTML ( )   PDF (2824KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    A novel visible light-driven uric acid(UA) fuel cell was preprared by employing CdS nanoparticles modified indium-tin oxide photoanode(CdS/ITO) and [Cu(phen)(L-Trp)(H2O)]+(phen=1,10-phenanthrothine and L-Trp=L-tryptophan) modified single-walled nanotubes(SWCNTs) cathode. The CdS nanoparticles obtained after thermal treatment at 40 ℃ show obvious absorption and open-circuit photovoltage responses between 320 and 550 nm. The CdS/ITO electrode exhibits good photocatalytic activity towards the oxidation of uric acid(UA) upon visible light irradiation. The CdS nanoparticles prepared at high temperatures between 200 and 300 ℃ show smaller photocatalytic activities than those obtained at 40 ℃. The [Cu(phen)(L-Trp)·(H2O)]+/SWCNTs electrode exhibits a pair of quasi-reversible redox peaks at the formal potential of -0.131 V, indicating the electrocatalytic activity towards the reduction of both O2 and H2O2. Furthermore, on the basis of photocatalysis of CdS nanoparticles and electrocatalysis of [Cu(phen)(L-Trp)(H2O)]+, a photocatalytic UA(0.2 mmol/L) fuel cell was elaborately assembled, which showed an open-circuit photovoltage of 0.52 V, a short-circuit photocurrent of 13.08 μA/cm2 and a maximum power density of 13.08 μW/cm2 at 0.41 V upon the visible light irradiation of 0.18 mW/cm2.

    Preparation of Mesoporous Al2O3 with High Specific Surface Area by Evaporation-induced Self-assembly Stategy and Its Application as Ni-Al2O3 Catalysts for CO2-CH4 Reforming
    MO Wenlong, MA Fengyun, LIU Yue’e, LIU Jingmei, ZHONG Mei,
    2015, 36(12):  2475-2484.  doi:10.7503/cjcu20150444
    Asbtract ( )   HTML ( )   PDF (5472KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    To improve the catalytic performance of nickel-based catalysts for carbon dioxide reforming of methane, four supports, PA0.01, PA0.02, PA0.03 and PA0.05, were prepared by evaporation-induced self-assembly strategy, and the same contents of Ni of the four corresponding catalysts were prepared by hydrothermal-precipitation method. The catalytic performance of these samples for CO2-CH4 reforming was tested at 800 ℃. The supports and catalysts were characterized with ICP-AES, N2 absorption-desorption method, NH3-TPD, XRD, H2-TPR, TG-DTG and TEM techniques. It was shown that the specific surface area of PA0.02 was large(320.12 m2/g), and the corresponding PAC0.02 catalyst with area of 280.15 m2/g, which could provide more active sites and improve the activity of samples(the conversion of CH4 and CO2 of PAC0.02 was up to 91.92% and 94.69%); the reduction peak area of NiAl2O4 in PAC0.02 catalyst was higher than 80% of the total reduction area, indicating that the catalyst had better stability(the conversion of CH4 for PAC0.02 was about 50% after 154 h experiment).

    Preparation and Photoelectrochemical Properties of n-Type Macroporous Si/TiO2 Nanowire Heterostructure
    KOU Yanqiang, YANG Jikai, ZHU Lingxi, YU Changming
    2015, 36(12):  2485-2490.  doi:10.7503/cjcu20150378
    Asbtract ( )   HTML ( )   PDF (3597KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    n-Type macroporous silicon as substrate material was prepared by photo-assisted electrochemical etching. The TiO2 nanowire cover layer on macroporous silicon was prepared by hydrothermal method. Thus, n-type macroporous Si/TiO2 nanowire heterostructure was obtained. The formation of n-type macroporous Si/TiO2 nanowire heterostructure was confirmed by X-ray diffraction(XRD), scanning electron microscope(SEM), energy dispersive X-ray detector(EDX). The UV-Vis diffusion reflectance spectra showed that n-type macroporous Si/TiO2 nanowire heterostructure had the strongest absorption among the four tested samples. The photoelectric performance tests showed that n-type macroporous Si/TiO2 nanowire heterostructure had higher photocurrent than the n-type macroporous Si and the n-type Si/TiO2 nanowire. The results showed that n-type macroporous Si/TiO2 nanowire heterostructure as photoanode improved the performance of photoelectrochemical water splitting.

    QM/MM Molecular Dynamics Simulation on the Mechanisms for the Hydrolytic Deamination of Nicotinamidase
    DUAN Xinli, ZHANG Xin, LEI Ming
    2015, 36(12):  2491-2496.  doi:10.7503/cjcu20150365
    Asbtract ( )   HTML ( )   PDF (3904KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    The deamination process of nicotinamide to nicotinic acid by nicotinamidase simulated with combined QM(PM3)/MM molecular dynamics(MD) method. Our calculated results show that the whole mechanism includes four steps, transition of HS, nucleophilic attack by sulfur group, nucleophilic attack by hydroxyl group and proton transfer from Asp16 to Cys159. The rate-determined step is the nucleophilic attack by sulfur group. Through conformational analyses, we are able to indicate that high energy consumption mainly because the nucleophilic attack needs to break the hydrogen bond between substrate and Ala155. We suggest that mutation of the loop, which make Ala155 far from nicotinamide, could weaken the hydrogen bond and increase the reactivity of nicotinamidase. Based on this ground, release of ammonia and proton transfer processes are discussed in details. The results could give some useful suggestions to enzyme design and site-directed mutagenesis studies.

    Simulation on the Growth of NiCl2 Crystal
    XIAO Zhixia, ZHU Yanli, ZHAO Yong, XING Jiachao, JIAO Qingjie
    2015, 36(12):  2497-2503.  doi:10.7503/cjcu20150352
    Asbtract ( )   HTML ( )   PDF (3264KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Based on the density function theory(DFT) calculation of crystal faces (003), (101), (104), (018) and (113) of NiCl2 via CASTEP program, total energy, surface energy, band structures and density of states(DOS) were investigated. The crystal morphology of NiCl2 and the growth habit of the surface of NiCl2 were calculated by Bravais-Friedel Donnay-Harker(BFDH) rules. The results show that vacuum width of 0.6 nm and atom layer of 3 are reasonable to the surface energy calcution. The energy state of NiCl2 is far more stable when face (003) is mainly unfold faces, while the energy state would be instable when faces (101), (104), (018) and (113) are the mainly unfolded. The electric structure results show that the front valence electron of face (003) is active correspondingly. That is there may be some activity points on this face. The larger energy band gap of it shows that the inner electrons are more stable. The band structures and DOS analysis show that the number of high energy band of (003) slab near the Fermi energy is less than that of other slabs, which proves the system is more stable no thermodynamics when (003) is mainly unfold.BFDH calculation on NiCl2 predicts the unfold faces (003) and (101) successfully and indicates (003) is the most important face. Other results show that the growth habits of NiCl2 cell and its surface slabs are different, NiCl2 cell, (003), (101) and (113) slabs are inclined to form crystal with hexagonal plate and bulk shapes, (104) and (018) slabs are inclined to form crystal with rod shape.

    Terahertz Spectroscopic and Density Functional Theoretical Analysis of Cocrystal Between Olmesartan and Benzoic Acid
    FANG Hongxia, ZHANG Qi, ZHANG Huili, QIN Dan, HONG Zhi, DU Yong
    2015, 36(12):  2504-2510.  doi:10.7503/cjcu20150351
    Asbtract ( )   HTML ( )   PDF (3018KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    The structure of cocrystal between olmesartan and benzoic acid was deterimined via terahertz time-domain spectroscopy(THz-TDS) technique and density functional theory(DFT). Experimental results show that all of them have distinctive and different fingerprint spectra in the THz region. The absorption peaks of olmesartan were at 0.53, 0.98, 1.09 THz and the absorption peaks of benzoic acid were at 0.65, 0.89, 1.10 THz. Characteristic bands observing in the terahertz spectra of cocrystal were at 0.64 and 1.33 THz, which were greatly different from corresponding raw starting materials. According to the structural characteristic of olmesartan molecule, density functional theory(DFT) program was used to simulate molecular structures and corresponding frequencies of olmesartan and three possible cocrystal forms considering the position of hydrogen bond formation between olmesartan and benzoic acid. The theoretical result showed that simulated olmesartan molecule had absorption peaks at 0.76, 1.05 and 1.27 THz, which was agreement with the THz experimental result. In addition, the theoretical results of three possible simulated cocrystal structures showed that FormⅠof simulated cocrystal was much better agreement with the experimental result than others. Therefore, the structure of cocrystal was confirmed that the first hydrogen bond was formed between amino group of olmesartan and hydroxyl group of benzoic acid, while the second one was formed between nitrogen atom of five nitrogen ring in olmesartan and carbonyl group of benzoic acid. The characteristic absorption bands of cocrystal between olmesartan and benzoic acid were also assigned based on the simulation results of DFT calculation.

    Ag Through-void Arrays Prepared by Template Electrodeposition and Their Refractive Index Sensing Properties
    XU Die, SHEN Xiaohua, LI Huanhuan, DU Yuanchun, HU Jiawen
    2015, 36(12):  2511-2515.  doi:10.7503/cjcu20150328
    Asbtract ( )   HTML ( )   PDF (2975KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    One- and two-tier Ag through-void arrays for extraordinary optical transmission(EOT)-based plasmonic sensing were fabricated by electrodeposition of Ag through monolayer and bilayer colloidal crystal template of polystyrene spheres, followed by removal of the template. Experimental results reveal that compared with one-tier Ag through-void arrays, two-tier Ag through-void arrays show largely improved sensitivity and figure of merit(FOM), which reach 559.71 nm/RIU(RIU: Refractive index unit) and 14.28 RIU-1, respectively. These suggests a low cost, feasible way for the fabrication of high quality EOT-based plasmonic sensor using routine techniques in which the tools used are accessible to most researchers.

    Synthesis of Three-dimensional Graphene Electrodes and Their Applications in Capacitive Deionization
    CHEN Chunyang, YU Fei, ZHOU Huiming, CHEN Junhong, MA Jie
    2015, 36(12):  2516-2522.  doi:10.7503/cjcu20150325
    Asbtract ( )   HTML ( )   PDF (3264KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    In this paper, three-dimensional(3D) graphene hydrogel/aerogel were synthesized by wet chemistry methods, and then used as electrode materials in capacitive deionization(CDI) to separate NaCl from aqueous solution. Besides, the structure and character of the electrodes were analyzed by scanning electron microscopy, cyclic voltammetry, X-ray photoelectron spectroscopy and other methods. The results show that 3D graphene hydrogel has larger adsorption capacity than graphene aerogel. Then the graphene hydrogel electrode was optimized by pressing graphene hydrogel(pressing hydrogel). 3D graphene electrodes achieve good results in capacitive deionization. And the adsorption capacity ranking from big to small is pressing hydrogel, graphene hydrogel, graphene aerogel.

    Segregation and Stability of Cu-Fe Alloy Nanowires Encapsulated in Carbon Nanotubes
    TIAN Mingli, SONG Yueli, WAN Mingli, LI Yong, JI Pengfei, ZHOU Fengqun
    2015, 36(12):  2523-2531.  doi:10.7503/cjcu20150313
    Asbtract ( )   HTML ( )   PDF (7662KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Molecular dynamics simulations were performed to investigate the structures of Cu-Fe alloy nanowires encapsulated in carbon nanotubes(CNTs). Simulated annealing method was employed to find the stable structure at 300 K. We found that all Cu-Fe atoms in CNTs were arranged in a series of concentric cylindrical layers even they had different contents, and a significant segregation was found. In these stable structures, Cu atoms are apt to stay at the surface shells, while Fe atom prefer to stay at the core shells. The degree of segregation is associated obviously with the CNTs diameter and the alloy fractions, but less dependents on the metal atom numbers. Both the larger diameter of CNTs and bigger content of Cu atoms result in more significant segregation. The results suggest that Cu-Fe alloy nanowires with pure Cu shell and pure Fe core or alloy core inside CNTs could produce by tuning alloy fractions. In addition, we also analyze the system stability by comparing average potential energy of each atom. The studies show that the larger diameter of CNTs, greater numbers of metal atoms and bigger content of Fe atoms result in much better stability. We also found that changing the length and chirality of the CNTs modifies the results only slightly.

    Monte Carlo Simulation of Effects of Homopolymer Chain Length on Interfacial Properties of A/AB/B Ternary Polymer Blends
    LIU Dongmei, DUAN Xiaozheng, SHI Tongfei, JIANG Fang, ZHANG Hanzhuang
    2015, 36(12):  2532-2539.  doi:10.7503/cjcu20150297
    Asbtract ( )   HTML ( )   PDF (4721KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    We employed Monte Carlo simulation to investigate the effects of chain length of the homopolymer on the interfacial properties between two immiscible homopolymers. When the chain length of diblock copolymer is fixed at NC=20, as the chain length(NH) of homopolymer increases from 10 to 60, the interface thickness increases significantly. The orientation parameter q of the diblock copolymer chain decreases with the increase of NH from 10 to 40, but enlarges with the further increase of homopolymer chain length, which means that the stretching of diblock copolymer displays a non-monotonic dependence on the homopolymer chain length. When the diblock copolymer chain length is fixed as NC=60, as the chain length of homopolymer increases from NH=10 to 60, the interface thickness decreases and the diblock copolymer chain orientation parameter q decreases, indicating that the stretching of diblock chain is weakened.

    Chloride-free CuY Catalyst Prepared by Solid State Reaction for Oxidative Carbonylation of Methanol— Effect of Solid State Reactive Temperature and Copper Loading
    WANG Yuchun, ZHENG Huayan, LIU Bin, ZHANG Guoqiang, LI Zhong
    2015, 36(12):  2540-2549.  doi:10.7503/cjcu20150285
    Asbtract ( )   HTML ( )   PDF (3725KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Copper(Ⅱ) acetylacetonate Cu(acac)2 as copper source and NH4Y zeolite as support, the chloride-free CuY catalyst was prepared by solid state reaction. The influence of the solid state reactive temperature and the copper loading(mass fraction) on the catalytic activity for oxidative carbonylation of methanol was studied. And the effect of the phase structure, reducible copper species and texture on catalytic activity was investigated. The results indicates that the exchange degree between NH4+ and Cu2+ at first increases and then decreases with the increasing of the solid state reactive temperature, and the catalytic activity of the as-prepared CuY catalyst has the same changing tendency. When copper loading is below 10%, the selectivity of dimethyl carbonate is low by the effect of the residual Brϕnsted acid. However, copper loading is above 12%, the unexchanged Cu(acac)2 decomposed to form CuO nano-particles and the nanometer-sized particles grow up, covered some active centers, even blocked pore, resulting in the decrease of catalytic activity. The as-prepared CuY catalyst with 12% copper loading at 250 ℃ solid state reaction exhibits an excellent catalytic activity. Space-time yield(STY) of dimethyl carbonate(DMC) up to 267.3 mg·g-1·h-1 was achieved.

    Synthesis of Mixed Alumina Silica Pillared Zirconium Phosphate and Its Catalytic Performance in Epoxidation of Soyate
    LIU Wenjin, WANG Hongning, CHEN Ruoyu
    2015, 36(12):  2550-2556.  doi:10.7503/cjcu20150155
    Asbtract ( )   HTML ( )   PDF (2802KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    The mixed alumina-silica pillared zirconium phosphate material was synthesized by template-directing self-assembly method. The textural properties of the material was systematically characterized by X-ray diffraction(XRD), Brunauer-Emmett-Teller(BET), Field emission scanning electron microscope(FESEM) and 27Al Nuclear magnetic resonance(27Al NMR). The formation mechanism of the mixed alumina-silica pillared zirconium phosphate was further studied. The results show that the aluminum source is presented as etrahedral aluminum grafted onto the gallery and the octahedral aluminum on the layer, repectively. In the evaluation of catalytic performance, the epoxidation reaction of soyate is used to study the mixed alumina-silica pillared material. It exhibits 91.7% epoxy selectivity. The analysis of the catalytic behavior indicate that the ordered interlayer structure given by the template-directing self-assembly method provokes an adequately contact between the relatively large reactants of methyl soyate and the active sites. With the FTIR spectra of adsorbed pyridine and the analysis of the reaction kinetics, it can be found that the excellent catalytic performance compared with the pure silica pillared zirconium phosphate material and other solid acids is due to the abundant Lewis sites arising from the introducing of the alumina source.

    Polymer Chemistry
    Synthesis and Characterization of Poly(acrylonitrile-co-itaconate)-graft-Poly(ethylene glycol) Copolymers as Novel Solid-Solid Phase Change Materials for Thermal Energy Storage
    MU Siyang, GUO Jing, QI Shanwei, ZHANG Bo, ZHANG Hong, YU Yue
    2015, 36(12):  2557-2562.  doi:10.7503/cjcu20150655
    Asbtract ( )   HTML ( )   PDF (3995KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    The core of this study firstly synthesizes an “active” matrix materials with the itaconic acid containing double-carboxyl end group and acrylonitrile copolymer through molecular design. Then, the poly(ethy-lene glycol)(PEG) was grafted to the poly(acrylonitrile-co-itaconate)[P(AN-co-IA)] using methylenediphenyl diisocyanate(MDI) as a bridge-base and cross-linking agent. The poly(acrylonitrile-co-itaconate)-graft-poly(ethylene glycol)[P(AN-co-IA)-g-PEG] solid-solid phase change materials(SSPCMs) were obtained in this paper. Furthermore, the chemical structure, crystallization properties, thermal energy storage properties , crystallization process, thermal stabilities, and hydrophilic property of the SSPCMs were investigated using Fourier transform infrared, differential scanning calorimetry, wide-angle X-ray diffraction, polarized optical microscopy, thermogravimetric analysis and water contact angle, respectively. The results showed that these SSPCMs had the characteristics of solid-solid phase change, excellent energy storage properties and latent heat of 70 J/g or more. The crystalline morphology and crystal structures of the synthesized SSPCMs are difference from PEG and P(AN-co-IA). Moreover, The SSPCMs have a good thermal stability and the initial decomposition temperature(Td) is 289 ℃, and the hydrophilic property of the blend membrane were improved, the water contact angle minimum can be achieved at 33.71°.

    Synthesis and Drugloading Properties of Dual Thermo and Redox Sensitive P(NIPAM-AA) Nnanogels
    ZHAN Yuan, HE Peixin, SUN Zhengguang, YI Panpan, ZHANG Weili, ZHANG Yuhong, LI Yulin
    2015, 36(12):  2563-2568.  doi:10.7503/cjcu20150580
    Asbtract ( )   HTML ( )   PDF (2853KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Although doxorubicin(DOX) has been widely used in the treatment of different types of cancer, the multi-drug resistance is still a bottle for its further clinical applications. Nanogels with high loading capacity, good stability, environmental responsiveness(such as ionic strength, pH, temperature, reducing agent), are promising therapeutic nanocarriers for targeting delivery of drugs in a controllable way. In this study, a series of thermo- and redox- sensitive P(NIPAM-AA) nanogels was developed by free radical precipitation polymerization of N-isopropylacrylamide(NIPAM) and acrylic acid(AA) as monomers in the presence of N,N'-bis(acryloyl)cystamine(BAC) as crosslinking agent. The structures, particle size, Zeta potential, morphology, encapsulation efficiency and drug cumulative release[using doxorubicin(DOX) as an anticancer model drug] of the prepared composite nanogels were characterized by FTIR, Raman spectrum, dynamic light scattering(DLS), scanning electron microscopy(SEM) and ultraviolet-visible(UV-Vis) techniques. DLS study showed that BAC concentrations had great influence on thermo-sensitivity of nanogels as well as their Zeta potentials. UV-Vis study showed that when concentration of BAC was 1.6 and 0.32 mmol/L, nanogels had good drug encapsulation efficiency(64.9% and 53.5%, respectively). In vitro release study showed that temperature controlled DOX release was not obviously(DOX cumulative release at 4 h was 56% and 58% at 25 and 37 ℃, respectively) for the 0.32 mmol/L BAC-crosslinking system, probably because of the loose structure of the nanogels at low crosslinking degree that allows for rapid DOX diffusion from the nanogels at both temperatures. When BAC concentration was increased to 1.6 mmol/L, DOX cumulative release at 4 h was 56% and 61% at 25 and 37 ℃, respectively. The release rate can be further accelerated in a medium mimicking the intracellular reductive environment(37 ℃ and in the presence of 4 mmol/L D,L-dithiothreitol). The nanogels with good thermo- and redox-sensitivity can act as a good platform for delivery of various kinds of therapeutics, beyond anticancer drugs.

    Effect of Metal Oxide Supported on Active Carbon on Vulcanization, Combustion and Thermal Ageing Properties of Flame Retardant Rubber
    PENG Hui, ZHOU You, HAO Jianwei, LI Zhuoshi, ZOU Hongfei
    2015, 36(12):  2569-2575.  doi:10.7503/cjcu20150583
    Asbtract ( )   HTML ( )   PDF (6928KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    With the excellent catalytic synergistic flame retardancy of metal oxide(MO) and its effect of improving the thermal ageing property as well as the porous and large specific surface area characteristic of bamboo based active carbon(AC), a series of metal oxide(Fe2O3, CuO, ZnO) supported on active carbon(AC-MO) synergist was prepared by solvent evaporation method. The vulcanization, combustion, thermostability, and thermal ageing properties for synergistic intumescent flame retardant ethylene vinyl-acetate copolymer rubber(EVM) with AC-MO and ammonium polyphosphate/dipentaerythritol was studied. The results showed that AC-MO was the target product and MO dispersed well when supported on AC. AC and AC-MO had a uniform dispersion in the flame retardant EVM. The introduction of AC-MO improved the maximum torque, flame retardancy, and char residue, especially for AC-Fe2O3. A Fe2O3 supported on AC improved its catalytic charring effect, which improved the integrity and compactness of char residue of flame retardant EVM. As a result, the flame retardancy was improved. After thermal ageing test, the tensile strength of EVM/IFR/AC-MO increased while the elongation at break decreased.

    Evolution of PMMA Latex During Solvent Annealing Process
    ZHENG Nan, LIU Jiaxue, CHEN Ran, LAI Yuqing, MEN Yongfeng
    2015, 36(12):  2576-2581.  doi:10.7503/cjcu20150565
    Asbtract ( )   HTML ( )   PDF (4395KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    A mono-dispersed poly(methyl methacrylate)(PMMA) latex dispersion was synthesized by emulsion polymerization. Small angle X-ray scattering technique was applied to determine the particle size and size distribution of the PMMA latex dispersion. The PMMA latex film was prepared by casting the diluted dispersion on a silicon substrate. Spectroscopic ellipsometer and scanning electron microscope were used for the investigation of the thickness and structure variations of the prepared latex film during two kinds of solvent annealing processes. When the PMMA latex film was annealed in the relatively good solvent vapor, such as acetone, there were two processes during solvent annealing: particle deformation and swelling. And when the PMMA latex was annealed in relatively poor solvent vapor, such as ethanol, there was only one process: the swelling process.

    Fabrication and Characterization of PLGA-based Supermolecular Hydrogel
    LI Guifei, WU Jie, WANG Bo, ZHANG Weijun, YAN Shifeng, YIN Jingbo
    2015, 36(12):  2582-2589.  doi:10.7503/cjcu20150551
    Asbtract ( )   HTML ( )   PDF (4461KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Supermolecular hydrogels composed of cholesterol-modified triblock polymers poly(L-glutamic acid)-poly(ethylene glycol)-poly(L-glutamic acid)[(PLGA-b-PEG-b-PLGA)-g-Chol] and β-cyclodextrins(β-CD)-modified poly(L-glutamic acid)(PLGA-g-β-CD) were fabricated by host-guest interaction between cholesterol(Chol) and β-CD. This study presented the influence of concentrations and molar ratio on mechanical strength, PLGA molecular weight on mechanical strength, pore size, swelling ratios and biodegradability. The results showed that storage modulus was highest at concentrations of 150 g/L and Chol/β-CD molar ratio of 1:1. The average pore size of PLGA-based supermolecular hydrogels fabricated from concentrations of 150 g/L was between 10—30 μm. Swelling ratio was between 16%—32.5%. Degradation time could be controlled PLGA molecular weight from 40 d to 72 d. The excellent self-healing ability of hydrogels was performed. The cytotoxicity evaluation was observed that the adipose-derived stem cells treated with the polymers remained almost 100% viable, indicating good cytocompatibility of the hydrogels.

    Immobilization of Papain with Ionic Liquids-regenerated Cellulose Membrane for Wool Fabric Modification
    LI Qiujin, ZHAO Zhiqi, YUAN Yamei, GONG Jixian, ZHANG Jianfei
    2015, 36(12):  2590-2597.  doi:10.7503/cjcu20150498
    Asbtract ( )   HTML ( )   PDF (5048KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    Ionic liquid(IL) 1-butyl-3-methylimidazolium chloride([Bmim]Cl) was used to dissolve microcrystalline cellulose Avicel to make IL-regenerated cellulose membrane for papain immobilization through silane modification method. It demonstrated that the immobilized papain could be obtained at the condition of 6.5%(mass fraction) Avicel/[BMIM]Cl for membrane as the solid support; 30% NH2(CH2)3Si(OC2H5)3 at 50 ℃ to functionalize the carrier; adsorbing for 3 h followed by cross-linking for 4 h at 50 ℃, pH=7.0 and enzyme concentration of 300 mg/mL, using 10%(volume fraction) glutaraldehyde as the cross-linker. After immobilization, papain was immobilized to the both sides of the regenerated cellulose membrane surfaces with high loading density. The immobilized papain could be limited on the wool fiber surface, only digesting the scale structure instead of native papain penetrating inside the fiber and generating the significant weight and strengthen loss.

    Effects of Adding Reduced-graphene Oxide/Polypyrrole Composites on the Structure and Properties of Calcium Phosphate Cement
    XIAO Zhenkun, YU Haoran, WU Tao, WANG Ruizhen, PENG Zhang, LU Xiaoying, WENG Jie
    2015, 36(12):  2598-2603.  doi:10.7503/cjcu20150417
    Asbtract ( )   HTML ( )   PDF (3490KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    With the piezoelectricity of natural bone, electrical stimulation has been widely used in clinic for promoting bone growth and reconstruction. It has special meaning to prepare a conductive biomaterial for bone repair. In this paper, reduced-graphene oxide(RGO)/polypyrrole(PPy) composites with high conducity were added in the solid phase of calcium phosphate cement(CPC) and the effect of this addition on the structure and properties was investigated. The composites had great impact on physicochemical properties of CPC. The results showed that the setting time of CPC significantly decreases with RGO/PPy adding. It has great influence of adding RGO/PPy on the mechanical properties and conductivity of CPC, but no obvious effect on the phase composition of CPC. The conductivity of CPC gradually increases with the increase of RGO/PPy adding amount, and the compressive properties show opposite results with RGO/PPy addition. It has a dependent relationship between the adding amount of RGO/PPy and the conductivity and compressive mechanical properties.

    pH-Dependent Specific Protein Recognition Ability of Glycopolymers
    SONG Rongguang, ZHOU Yihan, LI Fan, WANG Haiyan, SHI Tongfei, ZHANG Guo
    2015, 36(12):  2604-2609.  doi:10.7503/cjcu20150350
    Asbtract ( )   HTML ( )   PDF (2519KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    A new di-block glycopolymer, poly(gluconamidoethylmethacrylate)-b-poly[2-(diethylamino)ethyl methacrylate]-co-poly[2-(dimethylamino)ethyl methacrylate][PGAMA-b-P(DMAEMA-co-DEAEMA), PGME] was synthesized. The chemical composition and the molecular weight of the glycopolymer were characterized by nuclear magnetic resonance(1H NMR) and gel permeation chromatography(GPC). The interactions of PGME and proteins were investigated by monitoring the turbidity value of the mixture solutions. PGME showed the specific biomolecular recognition ability with Concanavalin A compared with bovine serum albumin(BSA) at pH=8.3. When the environmental pH value changed to 7.3, the ability of PGME specific biomolecular recognition was suppressed and PGME exhibited the behavior of non-specific binding with bovine serum albumin and Concanavalin A. Dynamic light scattering and atomic force microscopy(AFM) tests were performed to investigate the properties of the PGME-protein complex aggregations, it would be a promising to design pH-sensitive drug delivery system of saccharides.

    Relaxation Process of Linear Polymer Chain in Post Array
    HOU Jixuan, HUANG Ziwen, LI Mingze, CHEN Yao, XIAO Yitong, ZHANG Yehui, YANG Jing
    2015, 36(12):  2610-2614.  doi:10.7503/cjcu20150268
    Asbtract ( )   HTML ( )   PDF (2087KB) ( )  
    Figures and Tables | References | Related Articles | Metrics

    We present an extensive set of simulation results for the relaxation processes of linear polymer chains embedded in post arrays using Monte Carlo algorithm. The comparison of different end-to-end relaxation functions shows that polymer chains exhibit reptation in post arrays. The relaxation is almost pure reptation for small array spacing while contour length fluctuation plays a role for large array spacing.