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71.
Seong‐Ho Choi Min‐Seok Kim Jae Jeong Ryoo Kwang‐Pill Lee Hyun‐Dong Shin Sun‐Hwa Kim Yong‐Hyun Lee 《应用聚合物科学杂志》2002,85(11):2451-2457
Carboxylic acid groups were introduced onto polyethylene (PE) film by radiation‐induced graft copolymerization. Subsequently, the clodextrin glucanotransferase (CGTase) was immobilized on the PE film with a carboxylic acid group. The activity of the immobilized CGTase on PE film was in the range of 0.40–1.04 U/cm2 per min. The production of cyclodextrins (CDs) from corn starch was examined using the CGTase‐immobilized PE film. The production ratios of CDs using CGTase‐immobilized PE film was in the following order: α–CD > β–CD > γ–CD. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 2451–2457, 2002 相似文献
72.
The aromatic‐aliphatic copolyamides were synthesized by condensation polymerization of aromatic diamine PPD (or APS, where PPD is p‐phenylene diamine and APS is aminophenyl sulfone), aliphatic diamine HDA (or EDA, where HDA is hexanediamine and EDA is ethylenediamine), and TPC (where TPC is terephthalyl chloride) with different molar ratios of aromatic diamine to aliphatic diamine. The steady‐state fluorescence of these condensed copolymers was investigated. These copolyamides exhibit strong blue‐to‐green fluorescence. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 315–321, 2005 相似文献
73.
74.
Jing Zhang 《Electrochimica acta》2006,51(20):4262-4270
A copolymer, poly(aniline-co-m-aminophenol), has been synthesized using repeated potential cycling. The monomer concentration ratio, acid concentration and applied potential strongly affect the copolymerization rate and the properties of the copolymer. The optimum conditions for the copolymerization are that the scan potential range is controlled between −0.10 and 0.95 V (vs.SCE), and a solution consists of 0.34 M aniline, 0.012 M m-aminophenol and 2 M H2SO4. The IR spectra of the copolymers demonstrate that the m-aminophenol units are included in the copolymer chains. The cyclic voltammograms of the copolymers in 0.3 M Na2SO4 solution with various pH values were performed at the potential ranges from −0.20 to 0.80 V and at a scan rate of 60 mV s−1. The results indicate that the copolymer still hold 41.7% of the electrochemical activity when the copolymer electrode was transferred from a solution of pH 5.0 to a solution of pH 11.0 in the potential range of −0.20 to 0.80 V. An impedance plot of the copolymer in a solution with pH 12.0 and at 0.40 V is constructed of a semicircle and a Warburg line with a slope of 1. This means that the electrode reaction of the copolymer at pH 12.0 is also under mass transfer control. The conductivity of the copolymer prepared under the optimum conditions is 1.42 S cm−1, and slightly depends on the pH value. Thus, the pH dependence of the electrical properties of the copolymer is improved compared with poly(aniline-co-o-aminophenol), and is much better than that of the parent polyaniline. 相似文献
75.
76.
新型后过渡金属烯烃催化剂的研究进展 总被引:1,自引:0,他引:1
综述了近年来-系列新型α-二亚胺型后过渡金属(Ni、Pd、Fe、Co)催化剂在烯烃聚合、极性单体共聚、烯烃齐聚、环烯烃加成聚合、烯烃活性聚合和聚烯烃纳米复合物等方面的最新进展。系统地阐述了不同的中心过渡金属离子、α-二亚胺骨架、骨架上的取代基和不同的聚合条件(温度、压力)分别对催化剂的聚合活性、聚烯烃支化率、聚合物分子量和分子量分布以及聚合产物的性质等影响,并且简要说明了这一类催化剂的制备方法和新特点。 相似文献
77.
Soap‐free emulsion copolymerization of perfluoroalkyl acrylate (FA)/methyl methacrylate (MMA)/n‐butyl acrylate (n‐BA) was carried out in the presence of sodium 2‐acrylamide‐2‐methyl propanesulfonate (AMPSNa) as a reactive surfactant and potassium persulfate (KPS) as an initiator. An analysis of the effects of concentration of AMPSNa, KPS, FA as well as polymerization temperature on the kinetic features (rate of polymerization) and colloidal characteristics (mean particle diameter, particle disperse index, particle numbers, and surface charge density) was followed. NMR, FTIR, AFM, and fluorine‐selective electrode analysis were used to characterize the composition and morphology of the FA copolymers. Both AFM analysis and contact angle measurements strongly implied that the fluorinated segments migrated to the outmost surface and created films with lower surface energy. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 2438–2444, 2007 相似文献
78.
In the present study, the effects of charge‐transfer complex formation and intramolecular fragmentation (side‐chain lactonization) in radical copolymerization of tert‐butyl vinyl ether (t‐BVE) with anhydrides of maleic (MA) and citraconic (CA) acids and the structure–thermal behavior relationships of the resulting copolymers were examined using the 1H‐NMR, FTIR, DSC, and TGA analysis methods. It was shown that copolymerization under the chosen conditions proceeded through intramolecular fragmentation with the formation of γ‐lactone units. Side‐chain fragmentation of t‐BVE–MA and t‐BVE–CA copolymers also was confirmed by TGA and DSC analysis. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 2455–2463, 2006 2006 相似文献
79.
80.
High‐performance shape‐memory polyurethane block copolymers, prepared with two types of poly(tetramethylene glycol) (PTMG) used as soft segments, were investigated for their mechanical properties. Copolymers with a random or block soft‐segment arrangement had higher stresses at break and elongations at break than those with only one kind of PTMG. Random copolymers with fewer interchain interactions showed higher elongation than block copolymers. All the copolymers had shape‐recovery ratios higher than 80%. In dynamic mechanical testing, the glass‐transition behavior clearly depended on the soft‐segment arrangement: random copolymers had only one glass‐transition peak, whereas block copolymers showed two separate glass‐transition peaks. Overall, the control of the soft‐segment arrangement plays a vital role in the development of high‐performance shape‐memory polyurethane. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 2410–2415, 2004 相似文献