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排序方式: 共有88条查询结果,搜索用时 31 毫秒
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Surface composition and property of film prepared with aqueous dispersion of polyurethaneurea-acrylate including fluorinated block copolymer 总被引:1,自引:0,他引:1
The aqueous dispersion of polyurethaneurea-acrylate (PUA) including small amount of fluorinated block copolymers containing carboxyl groups (PATF), which can be dissolved in water, was used to make films and the surface properties of these films were examined. The experimental data show that the modified PUA film exhibits a hydrophobic surface property, although the original surface of PUA film is hydrophilic. The surface composition of the modified PUA film was measured by ATR and XPS. The results indicate that there is a concentration gradient of the fluorine groups along the lines of thickness of the modified film and towards the outmost surface layer, resulting from the migration of fluorinated blocks to the air side surface of the modified PUA film during the film formation process. However, the PUA film can not be modified effectively by adding the sodium salt of PATF, since the urethane groups in the system are easy to occupy on the surface of the film. 相似文献
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M. N. Chai 《International Journal of Polymer Analysis and Characterization》2013,18(4):280-286
Electrical impedance spectroscopy was used to measure the conductivity of solid polymer electrolytes. From the impedance study, the highest ionic conductivity of solid polymer electrolytes based on carboxyl methylcellulose as polymer host and oleic acid as the doping salt, prepared by the solution casting method at room temperature, σr.t, is 2.11 × 10?5 S cm?1 for the sample containing 20 wt.% of oleic acid. Transference number measurement was performed to correlate the diffusion phenomena to the conductivity behavior of carboxyl methylcellulose-oleic acid solid polymer electrolytes. From the transference number measurement study, the conduction species carrier of the cation (+) is higher than that of the anion (?). Thus, the results proved that the samples are proton-conducting solid polymer electrolytes. 相似文献
5.
M. N. Hafiza A. N. A. Bashirah N. Y. Bakar 《International Journal of Polymer Analysis and Characterization》2014,19(2):151-158
This present work discusses dual-blend green polymer electrolyte (GPE)–based natural polymers, composed of carboxyl methylcellulose (CMC) and chitosan (CS), created by introducing various compositions of ammonium bromide (NH4Br) as a dopant in the system. These GPEs were successfully prepared by the solution casting technique and characterized using electrical impedance spectroscopy (EIS). From EIS measurement, the highest room-temperature conductivity is 1.21 × 10?5 Scm?1 for the sample containing 20 wt.% of NH4Br. Plot of the temperature dependence of the GPEs revealed that the system obeys the Arrhenius rule and was thermally assisted. Besides that, dielectric studies were also conducted and the data were analyzed using complex permittivity, ?*, and complex electrical modulus, M*, to determine the sample with the highest conductivity value. Thus, this study confirmed non-Debye behavior in the sample. 相似文献
6.
以含羧基侧基的聚芳醚酮酮醚酮酮(PEKKEKK-A)树脂为原料,二氯亚砜(SOCl2)、二氯乙烷(DCE)、吡啶为催化溶剂体系,合成带甲酰氯侧基的聚芳醚酮酮醚酮酮(PEKKEKK-C)树脂.PEKKEKK-C与甲醇、乙醇、丁醇、辛醇、苯酚等发生酯化反应,得到5种含羧酸酯侧基的聚芳醚酮酮醚酮酮(PEKKEKK-E)s.用红外光谱(FTIR)、氢核磁谱(1H-NMR)、广角X射线衍射(WAXD)、热失重(TGA)、示差扫描量热(DSC)等技术对其结构与性能进行了分析表征.结果表明,聚合物为非晶聚集态;玻璃化转变温度(Tg)在175.7~236.8℃之间,较PEKK有较大幅度提高;出现两次热失重平台,分别在335~365℃,460~505℃之间,第一次失重可能由于酯分解所致,第二次失重可能是分子主链开始分解;树脂能溶解于DMAc、NMP、二氯甲烷等普通有机溶剂中,溶剂挥发后成膜性良好,可制成透明薄膜;断裂伸长率在6.34%~15.43%之间,拉伸强度在74.68~85.35MPa之间。 相似文献
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N-tert-Butylamides are readily converted into the corresponding carboxylic acids by simple nitrosation. The process, which occurs under mild nonaqueous conditions, leaves carboxylic esters untouched and transforms multicomponent reaction products into useful building blocks for further synthetic elaboration. 相似文献
9.
Anionic groups (AGs) on different cellulosic fiber surfaces were investigated by methylene blue (MB) and polyelectrolyte (PE) sorption, X-ray photoelectron spectroscopy (XPS), and total attenuated reflectance infrared spectrometry (FTIR-ATR). The MB sorption isotherms fitted well the Langmuir equation that gave consistent estimations of sorption capacities. FTIR-ATR showed that MB molecules had extensive accessibility to the fiber wall pores. Estimation of surface AGs by PE sorption gave much higher values than a new method combining MB sorption and XPS measurements (MB-XPS). The surface AGs in different cellulosic fibers accounted for 1-3% of the total AG content as revealed by MB-XPS. It was suggested that PE molecules can penetrate the fiber wall and form loops or unattached segments at external fiber surfaces that disrupt the PE sorption stoichiometry. The competition of MB and PE for the anionic sites in papermaking was assessed and it was shown that MB ions have a much stronger affinity to AGs than PE molecules. 相似文献
10.
Sifang Kong Jiang Cheng Yangsheng Liu Xiufang Wen Pihui Pi Zhuoru Yang 《Central European Journal of Chemistry》2008,6(4):627-633
In this study, a novel and effective suspension polymerization has been employed to prepare functional magnetic porous SrFe12O19/P(St-DVB-MAA) microspheres in the presence of bilayer surfactants (sodium dodecyl benzene sulfonate (SDBS) and oleic acid
(OA)) coated on micro-size magnetic SrFe12O19. This was achieved by pre-polymerizing the organic phase, which contained co-monomers, porogens and treated magnetic particles,
at 65°C for 0.5 h under ultrasound conditions. Aqueous solutions containing a dispersion agent were then added to effect suspension
polymerization. Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD),
thermogravimetric analysis (TGA) and magnetic property measurement system (MPMS) were used to characterize the functional
magnetic porous microspheres. The results show that the microparticles are well shaped with a uniform size distribution of
about 0.5 ∼ 0.7 mm and the surfaces of the microspheres have many micro-pores with an average diameter of 0.533 μm. There
are carboxyl groups (−COOH) on the surface of the microspheres to the extent of 0.65 mmol g−1, as determined by conductometric titration. According to the XRD spectra, iron oxide consists mainly of SrFe12O19 which reveals hexahedral structure. The content of magnetic SrFe12O19 reaches 17.81% (by mass), and the microspheres have good heat resistance. The magnetic porous microspheres are ferromagnetic
with high residual magnetization and coercivity, 21.59 emu g−1 and 4.13 kOe, respectively. The saturation magnetisation is around 42.85 emu g−1.
相似文献