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111.
R. Sakamoto 《Colloid and polymer science》1984,262(10):788-792
Solvent effects on the phase separation of poly(-benzyl L-glutamate) to liquid crystal and isotropic solution have been observed in various helicogenic solvents. The temperature-composition phase diagrams have been determined for each solution. The critical concentrations,
2
*
, at which the phase separation occours have been compared in various solvents. In dimethylformamide in which the polymer is molecularly dispersed, the observed
2
*
value has agreed with that calculated by Flory's theory. In some solvents in which the polymer aggregates in a head-to-tail mode such as chloroform, the observed
2
*
values have been considerably small. It is assumed that the polymer aggregates behave as longer particles than the original particles. In dioxane in which the polymer aggregates highly both in a head-to-tail and a side-by-side modes, the
2
*
value has been a little larger than that in chloroform. In this case the relationship between the aggregation and the liquid crystal formation is so complicated that further investigation is necessary. In aromatic solvents such asm-cresol that dissolves the polymer almost molecularly, the
2
*
is smaller than that in dimethylformamide. Therefore, the intermolecular interactions between the phenyl groups in the side groups of the polymer and those in solvent molecules must be considered.The author is grateful to Mr. K. Sano and Mr. M. Watanabe for their observation of the liquid crystal formation. 相似文献
112.
The stoichiometric solubility constant of eitelite (NaMg
0.5
CO
3
+2H+ ⇄ Na++0.5Mg
2+
+CO
2
(g)+H
2
O, log*K
pso
I
=14.67±0.03 was determined at I=3 m (mol kg−1) (NaClO
4
) and 25°C. The stability of magnesium (hydrogen-)carbonato complexes in this ionic medium was explicitely taken into account.
Consequently, trace activity coefficients of free ionic species, calculated from the Pitzer model with ion-interaction parameters
from the literature, were sufficient for an evaluation of the thermodynamic solubility constants and Gibbs energies of formation
for eitelite (−1039.88±0.60), magnesite (−1033.60±0.40), hydromagnesite (−1174.30±0.50), nesquehonite (−1724.67±0.40), and
brucite (−835.90±0.80 kJ-mol
−1
). The increasing solubilities of nesquehonite and eitelite at higher sodium carbonate molalities were explained by invoking
a magnesium dicarbonato complex (Mg2++2CO
3
2−
⇄ Mg(CO3)
2
2−
, log βz = 3.90 ± 0.08). A set of ion-interaction parameters was obtained from solubility and dissociation constants for carbonic
acid in 1 to 3.5 m NaClO
4
media
which reproduce these constants to 0.02 units in log K. The following Pitzer parameters are consistent with the previously
studied formation of magnesium (hydrogen-)carbonato complexes in 3m NaClO
4
. The model and Gibbs functions of solid phases derived here reproduce original solubility data (−log [H+], [Mg
2+
]
tot
) measured in perchlorate medium within experimental uncertainty.
Presented at the XXII International Conference on Solution Chemistry, July 14–19, 1991, Linz, Austria. 相似文献
113.
《Surface and interface analysis : SIA》2005,37(3):310-315
Carbon film coatings have been produced by a hot‐wall chemical vapor deposition (CVD) method under moderate conditions from pyrolysis of a mixture of propane and argon on an Fe(110) substrate at temperatures of 800–900 °C for different deposition times. The effects of temperature and reaction time on the growth of the carbon films were studied. Field‐emission scanning electron microscopy (FESEM), Raman microscopy, Auger electron spectroscopy (AES) and x‐ray diffraction methods have been performed to study the surface morphologies, growth features and microstructures of the carbon film coatings. The FESEM analyses indicated that carbon films on an Fe substrate consisted of flat‐layer and filamentous morphologies. Raman and AES analyses showed that the carbon initially was crystalline but the degree of disorder in the top layer of the carbon film increased with increasing deposition temperature. High‐resolution transmission electron microscopy studies are also in agreement with Raman results. The same trend was observed when the deposition time was increased from 5 to 30 min. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
114.
E. V. Tulyakova O. A. Fedorova Yu. V. Fedorov G. Jonusauskas A. V. Anisimov 《Russian Chemical Bulletin》2007,56(11):2166-2174
Using 1H NMR spectroscopy and steady-state and time-resolved electronic spectroscopy, the optical properties of mono-and bis(styryl)pyridinium
perchlorates and their complexes with Mg2+, Ba2+ cations were studied. The stability constants of the complexes were determined using spectrophotometric titration. The formation
of inclusion complexes for Mg2+ and sandwich type complexes for Ba2+ results in fluorescence enhancement and increases the lifetimes of the excited states of the initial bis-styryl ligands.
The variation of position of the styryl fragment in the pyridinium aromatic ring gives rise to photochromic crown ethers with
different optical and photophysical characteristics and is also an easy route to bis(crown-ethers) of symmetrical and unsymmetrical
structure.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2092–2100, November, 2007. 相似文献
115.
钯催化下有机锡化合物的偶联反应在碳-碳键形成过程中的应用 总被引:2,自引:0,他引:2
本文述评了最近几年来钯催化的有机锡化合物与有机亲电试剂的交叉偶联反应在有机合成中用于碳-碳键形成的主要研究成果。主要讨论了直接交叉偶联反应,CO或烯键插入的交叉偶联反应和机理。 相似文献
116.
Yoshitaka Gotoh Yutaka Kohno Wakichi Fukuda Masao Tomoi 《Journal of polymer science. Part A, Polymer chemistry》1994,32(8):1543-1550
Soluble polystyrenes with crown ether structures and hydroxyl groups adjacent to the macrorings were prepared by the reaction of epoxide-containing polystyrenes with monoaza-15-crown-5 or monoaza-18-crown-6. Rate of formation of the polymer-bound alkali cation-crown alkoxide ion pair from the soluble polystyrenes and aqueous NaOH or KOH depended on the loading of crown ether and hydroxyl units and on the size of the macroring. The elimination of HCl from less reactive 2-chloroethylbenzene with aqueous NaOH or KOH in the presence of the soluble polystyrene catalysts under two-phase conditions was limited mainly by the intrinsic reaction rate. The elimination of HBr from more reactive 2-bromoethylbenzene in the presence of the less (11%) ring-substituted polymer catalyst with 18-crown unit was limited by the alkoxide formation rate. © 1994 John Wiley & Sons, Inc. 相似文献
117.
Pengchong Li Zhi Shang Kejian Cui Huan Zhang Zhi Qiao Caizhen Zhu Ning Zhao Jian Xu 《中国化学快报》2019,30(1):157-159
Polystyrene (PS) fibers with core-shell structure were prepared by coaxial electrostatic spinning using liquid epoxy or curing agent as the core and PS solution as the shell. Scratch self-healing coatings were realized by using the healant-loaded core-shell fibers in the matrix. 相似文献
118.
Sumio Sakka 《Journal of Sol-Gel Science and Technology》1994,2(1-3):451-455
The present state of our knowledge on sol-gel coating films has been reviewed. A qualitative discussion is made on the limit of the film thickness which can be achieved in the sol-gel method and the factors affecting the film thickness. Considering that properties of the film are intimately related to the microstructure, types of microstructures accomplished by the sol-gel coating are introduced with examples. 相似文献
119.
S. Shen E. D. Sudol M. S. El-Aasser 《Journal of polymer science. Part A, Polymer chemistry》1994,32(6):1087-1100
The mechanism for the formation of micron-size polymer particles in the dispersion polymerization of methyl methacrylate was investigated by applying dynamic light scattering to monitor the evolution of the average particle size in the early stages of the polymerization. In addition, the contributions of physically adsorbed stabilizer and graft copolymer were evaluated by measuring the bound, unbound (adsorbed), and free stabilizer, and by determining the amount of added stabilizer required in seeded dispersion polymerizations. Twenty nanometer particles (termed nuclei) were the smallest particles detected and are considered to be formed by aggregation of growing polymer chains precipitating from solution as they exceed their critical chain length. Aggregation of these nuclei with themselves and their aggregates continues until mature and stable particles are formed. This occurs when sufficient stabilizer occupies the particle surface which includes both the polymeric stabilizer [poly(vinylpyrrolidone)] and its graft copolymer which is created in situ. The effects of process variables are discussed based on this mechanistic picture of the dispersion polymerization process. © 1994 John Wiley & Sons, Inc. 相似文献
120.
The micelle formation of nonyl-phenols with various numbers of ethoxy groups (n
EO=10–40) was investigated in aqueous solutions and the study was focussed on the effect of temperature (293–323 K), the chain length and the inorganic electrolyte (NaCl) on the critical micelle concentration (c.m.c).The c.m.c. was determined by surface tension and interfacial tension measurements in a water/n-octane system. On the basis of the actual c.m.c. and its temperature dependence the thermodynamic functions of micelle formation (H°
m,S°m,G°m) were also calculated. The latter study comprised the determination of the thermodynamic function for unity ethoxy groups ((Y°
m)) as a function ofn
EO.According to the experimental results the micellar solutions are the more stable, the smaller the number of ethoxy groups in the tenside molecule and the higher the temperature as well as the electrolyte content of the system. 相似文献