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《Surface and interface analysis : SIA》2003,35(10):852-855
Fluorocarbon–hydrocarbon microblock copolymers –(CF2)n–(CH2)m– (n = 4, 6, 8; m = 6, 8, 10) were synthesized. Binding energies of the C 1s and F 1s peaks of these copolymers were measured using x‐ray photoelectron spectroscopy. The binding energy of the C 1s peaks of the carbon atoms of the hydrocarbon segments was set at 285.0 eV as the binding energy reference. Unexpectedly, the binding energy of the C 1s peak corresponding to the CF2 group of the microblock copolymers was determined to be ~291.4 eV, which is ~0.8 eV lower than that of the CF2 group of tetrafluoroethylene. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
94.
Copolymers of ethyl cellulose (EC) with polystyrene (PSt) were synthesized through atom transfer radical polymerization (ATRP). The molecular weight of graft copolymers increased without any trace of the EC macro-initiator, and the polydispersity of the side chains was low. The molecular weight of the side chains increased with the monomer conversion. Kinetic study indicated that the polymerization was first order. The micelle characteristics of the graft copolymer in acetone were investigated using dynamic light scattering (DLS), atom force microscopy (AFM) and transmission electron microscopy (TEM). With increasing the concentration, micelles were gradually formed from the solution. The TEM and AFM images indicated that the micelles had spherical shape and showed core-shell structure. 相似文献
95.
Wei-ping Gao Yu Bai Er-qiang Chen~ 《高分子科学》2005,(3):275-284
Small fixed aggregates of a poly(ethylene oxide)-block-polybutadiene diblock copolymer(PEO-b-PB)in THFsolution were obtained by adding a selective solvent for PB blocks,followed by cross-linking the PB shells.Themorphologies of the nanostructured particles with a cross-linked shell were investigated by atomic force microscopy andtransmission electron microscopy.The average behaviors of the PEO crystallization and melting confined within thenanostructured particles were studied by using differential scanning calorimetry experiments.For the deeply cross-linkedsample(SCL-1),the crystallization of the PEO blocks was fully confined.The individual nanoparticles only crystallized atvery low crystallization temperatures(T_cs),wherein the homogenous primary nucleation determined the overallcrystallization rate.For the lightly cross-linked sample(SCL-2),the confinement effect was T_c dependent.At T_c(?)42℃,thecrystallization and melting behaviors of SCL-2 were similar to those of the pure PEO-b-PB diblock copolymer.At T_c>42℃,SCL-2 could form PEO lamellae thicker than those of the pure PEO-b-PB crystallized at the same T_c. 相似文献
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This work presents a method to separate polar naphthalenesulfonate (NS) isomers by capillary zone electrophoresis (CZE) with ultraviolet detection in industrial effluents and river water samples. The method involves extraction of samples by a polystyrene‐divinylbenzene copolymer (PS‐DVB) solid‐phase extraction (SPE) cartridge. The most effective CZE separation conditions were obtained in 20 mM borate buffer with 30% acetonitrile at pH 9.0 and 30 °C. The method proposed herein provides a high precision and sensitivity for NS isomers, to quantitation at ≤ 1.0 μg/L in 200 mL of the water samples. Recovery of the NS isomers in spiked water samples ranged from 73% to 87% while RSD ranging from 5.6 to 9.7%. The analysis of industrial effluents and river water samples was performed and naphthalene‐2‐sulfonate was found as a major pollutant. The difficulties in quantitating and identifying analytes in complex environmental samples can be resolved by using an internal standard response factor to calculate concentrations and relative migration times for peak confirmation. 相似文献
97.
聚丙烯-聚乙烯嵌段共聚物的分子结构及性能的研究 总被引:5,自引:1,他引:5
本工作用核磁共振(~(13)C-NMR)、示差扫描量热(DSC)、动态力学分析(DMA)和扫描电子显微镜(SEM)等技术研究了将丙烯、乙烯单体两步分段共聚、预期为聚丙烯-聚乙烯嵌段共聚物的合成物(简称为聚丙烯-聚乙烯嵌段共聚物或嵌段共聚物)。结果表明,在嵌段共聚物中含有一定量的、能为正庚烷抽提出来的乙丙无规共聚物(EPR);分段共聚的产物并非预想的PP-b-PE两嵌段共聚物,而是含有多种组分的共混物;形态表征的结果表明了嵌段共聚物为多相体系,EPR和PE形成分散相以球形无规分布于PP基体中。 相似文献
98.
The morphological changes with different compositions of casting solvents in the membranes of sulfonated polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene (SEBS) were investigated with small-angle X-ray scattering (SAXS) and transmission electron microscope (TEM). Using the single solvent of tetrahydrofuran (THF) and the solvent mixtures of methanol/THF with different compositions, the casting polymer solutions were prepared for the membrane fabrication. The proton conductivity and the methanol permeability of membranes were measured, and the effect of morphological changes on the casting solvents was discussed through Flory–Huggins theory. It was found that the sulfonated SEBS membranes were transformed from well ordered lamellar to disordered co-continuous structure and the morphological difference caused abrupt enhancement in the proton conductivity and the methanol permeability as the concentration of methanol in the mixed solvents (MeOH/THF) increased. 相似文献
99.
四氟乙烯和全氟4-甲基-3,6-二氧杂-△~7辛基磺酰氟在溶剂氟里昂-113(F-113)中进行自由基引发聚合反应时,共聚物(T-O)是否有链转移,可以通过测定所得共聚物中的含氯量来得以证实。我们首次应用质子X萤光分析法(PIXE)进行分析。结果表明,共聚物中含氯量小于1ppm,F-113溶剂并未发生链转移。同时,我们测定了已证明有F-113参与链转移反应的F_(40)试样,含氯量高达700ppm。 相似文献
100.