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91.
Quanwei?Yu Jens?Fr?mmel Thomas?WolffEmail author Karel?Procházka 《Colloid and polymer science》2004,282(9):1039-1043
Solid stoichiometric complexes of [3,12]-ionene and dodecyl sulfate form upon reaction of the bromide of the ionene and the silver salt of dodecyl sulfate in methanol. IR, DSC, and TG investigations indicated that the solid complexes are stable between 30 and 120 °C. TG and DSC also showed that the complexes easily take up water at ambient conditions. These samples are optically isotropic. When exposed to an increased humidity they exhibit optical anisotropy, i.e., birefringence, which is caused by the formation of a hexagonal mesogenic phase. Mesogenicity is necessarily accompanied by a further uptake of water (4–5 H2O molecules per ionic unit), which is dependent on the relative humidity. The phase behavior as a function of temperature and controlled relative humidity was studied using birefringence measurements and polarizing microscopy. 相似文献
92.
研究了水溶性钌-膦配合物催化肉桂醛选择加氢反应中,相转移剂和表面活性剂对反应转化率和选择性的影响,考察了表面活性剂CTAB(十六烷基三甲溴化铵)浓度以及影响两相界面性质的因素—水相和有机相体积比、有机溶剂的改变等的影响.结果表明,相转移剂可以促进反应进行,其中以季铵盐相转移剂最好;表面活性剂能够显著地加快反应,其中以阳离子表面活性剂的效果最佳,且分子中含有长链烷基者(如CTAB)效果更好,非离子和阴离子表面活性剂的效果较差;对于CTAB,其浓度的增加导致反应速度的明显加快,但CTAB浓度达到1.65×10-2mol/L之后,反应体系乳化严重,反应完成后,两相分离变得困难.而增加水相体积和加入适当的有机溶剂,有利于转化率和选择性的提高. 相似文献
93.
94.
Mineo Hashizume Isamu Saeki Masashi Otsuki Jun-Ichi Kikuchi 《Journal of Sol-Gel Science and Technology》2006,40(2-3):227-232
To extend the concept of the Cerasome, an organic-inorganic vesicular nanohybrid, this paper investigates the preparation
and characterization of a “mixed” Cerasome. The system consists of a Cerasome-forming lipid 1, a cationic synthetic lipid 2, and a zwitterionic phospholipid 3. Lipid mixtures of 1 and 2 or 1 and 3 were used to prepare the mixed Cerasomes. Their lipid distributions were examined using differential scanning calorimetry
(DSC), which showed that 1 and 2 (or 1 and 3) were phase-separated in the mixed Cerasomes. These results seem to be mainly attributable to the polymerizable nature of
1. Results of scanning electron microscopy (SEM) and energy-dispersive X-ray analysis (EDX) showed that 1 and 3 were both incorporated into a single Cerasome, not macroscopically separated to form separate vesicles from each lipid component.
Mixed Cerasomes of 1 and 2 showed high morphological stability against a membrane-solubilizing surfactant, incorporating up to 70% of 2. On the other hand, the mixed Cerasomes from 1 and 3 were less stable than the mixed Cerasomes from 1 and 2. This relative instability might be attributable to differences between the mixed Cerasomes from 1 and 2 and 1 and 3 in terms of their vesicular sizes, lipid domain sizes, and their relative effectiveness for siloxane network formation. These
results strongly support the formation of mixed Cerasomes that have lipid domains in-plane. Systems described in this study
are useful to prepare variously mixed Cerasomes that have different surface functionalities and in-plane lipid distribution,
but which have high morphological stability. 相似文献
95.
相反转技术制备环氧树脂水基体系——相反转过程的流变行为研究 总被引:18,自引:0,他引:18
对高乳化剂浓度下的相反转发展过程的流变行为进行了应力扫描、动态频率扫描实验表征.结果表明,乳化剂浓度较高时,体系发生完全相反转;体系在相反转点前为W/O结构,其粘度几乎不随剪切应力的改变而改变,表现为牛顿流体行为;体系在相反转点后为O/W结构,具有很高的粘弹性,并且在较高剪切应力下表现为典型的假塑性.这是由于高分子水基微粒间通过其表面覆盖的表面活性剂与水形成氢键而产生了一种静态结构,此结构在较高剪切应力作用下破坏而导致假塑性. 相似文献
96.
A novel homotrifunctional conjugation reagent, 1,3,5-tris-(N-maleimidomethyl)benzene has been synthesized in high yield with minimum purification. The reactivity of this compound was examined by using l-cysteine as a nucleophile. 相似文献
97.
F. Muktepavela M. Vasylyev A. Czerwinski Z. Rogulski 《Journal of Solid State Electrochemistry》2003,7(2):83-86
The humid air induced processes of embrittlement of the Sn–Al alloy and hydrogen emission have been investigated. Using the
secondary-ion mass spectrometry, X-ray, scanning electron microscopy and energy-dispersive X-ray spectrometry techniques it
was found that the brittleness is caused by a failure of phase adhesion due to accumulation of hydrogen and formation of oxidized
layers on phase boundaries during contact of the alloy with water vapour. Specific physical and electrochemical properties
of the Sn/Al phase boundary satisfy conditions for the formation of atomic hydrogen and its reaction with Sn. Electrochemical
corrosion plays an important role at the stage of formation of atomic hydrogen. The penetration of hydrogen and its accumulation
in the bulk of the alloy is due to the high energy of the phase boundary and the low energy of formation of unstable tin hydride.
Electronic Publication 相似文献
98.
Meier H Gerold J Kolshorn H Mühling B 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(2):360-370
Four OPV series 1-4 (a-d) with a terminal dialkylamino group as electron donor were prepared by Wittig-Horner reactions. To study the influence of the push-pull effect on the long-wavelength absorption, three of the four series contained terminal acceptor groups (CN, CHO, NO(2)). The length of the chromophores strongly affects the intramolecular charge transfer (ICT)-an effect which superimposes upon the extension of the conjugation. Increasing numbers n of repeat units cause an overall bathochromic shift for the purely donor-substituted series 1 a-4 a and the series 1 b-4 b with CN as weak acceptor. The two effects annihilate each other in the series 1 c-4 c with terminal CHO groups, so that the absorption maxima are almost independent of the length of the chromophore. A hypsochromic shift is observed for the series 1 d-4 d, which contains the strong acceptor group NO(2). This anomaly disappears on protonation of the dialkylamino group because the push-pull effect disappears in the ammonium salts. The results can be explained by semiempirical quantum mechanics (AM1, INDO/S). The HOMO-LUMO transition, which is mainly responsible for the ICT, becomes less important in the electron transitions S(0)-->S(1) when the distance between donor and acceptor is increased. The commonly used VB model, which contains an electroneutral and a zwitterionic resonance structure, is contrasted with a MO model with dipole segments at both ends of the OPV chains. The latter model turned out to be more appropriate-at least for donor-acceptor-substituted OPVs with n >/= 2. 相似文献
99.
Biodegradable polyurethanes are an interesting alternative to many applications that involve plastics since they can minimize environmental problems caused by the low rates of natural degradation of synthetic polymers. In addition, since waterborne polyurethanes are based on aqueous dispersions, they restrict the use of organic solvents during processing and application of the polymer, thus contributing furthermore to reduce environmental damage. In this work, aqueous anionic polyurethane dispersions (PUD) with tailorable susceptibility for hydrolysis were synthesized by progressively replacing polypropylene glycol (PPG) with a biodegradable polycaprolactone diol (PCL) as soft segments. The hard segments were formed by extending isophorone diisocyanate (IPDI) with hydrazine (HZ). Dimethylol propionic acid (DMPA) was used as ionic center and triethyl amine (TEA) as neutralizer. The degree of phase separation was evaluated mainly by infrared spectroscopy (FTIR) and small angle X-ray scattering (SAXS). The results indicated that phase separation between hard and soft segments of poly(ester-urethane) is more significant than that of poly(ether-urethane). Data obtained from SAXS experiments indicated that phase separation within soft domains can also be present in samples containing both polyester and polyether soft segments. Hydrolytic degradation of the polymers in buffer solution of pH 7.4 and alkaline solution was performed as an initial test. The results showed that the fraction of polyester soft segments in the polyurethanes can be used to tailor the susceptibility of the materials to hydrolytic attack. Polyurethanes having higher contents of polyester were more promptly hydrolytically degraded than polyurethanes containing only polyether segments. 相似文献
100.
LiMnC2O4(Ac) precursor in which Li+ and Mn2+ were amalgamated in one molecule was prepared by solid-state reaction at room-temperature using manganese acetate, lithium hydroxide and oxalic acid as raw materials. By thermo-decomposition of LiMnC2O4(Ac) at various temperatures, a series of Li1+y[Mn2−xLix]16dO4 spinels were prepared with Li2MnO3 as impurities. The structure and phase transition of these spinels were investigated by XRD, TG/DTA, average oxidation state of Mn and cyclic voltammeric techniques. Results revealed that the Li-Mn-O spinels with high Li/Mn ratio were unstable at high temperature, and the phase transition was associated with the transfer of Li+ from octahedral 16c sites to 16d sites. With the sintering temperature increasing from 450 to 850 °C, the phase structure varied from lithiated-spinel Li2Mn2O4 to Li4Mn5O12-like to LiMn2O4-like and finally to rock-salt LiMnO2-like. A way of determining x with average oxidation state of Mn and the content of Li2MnO3 was also demonstrated. 相似文献