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131.
The content and isotopic compositions of different sulphur species in pore-water and solid phases have been examined on five sediment cores taken from muddy sediment region in the Yellow Sea and the East China Sea. Relationships among these data have been investigated with the combination of morphology of mineral pyrite and organic matter so as to role out the diagenetic behaviour of sulphur species at the early stage of diagenesis in modern marine sediment and the origin of pyrite formation. 相似文献
132.
133.
A polyaluminum chloride (PAC) sample was prepared using a slow alkaline titration method. The Bio-Gel P-100 gel column chromatographic
technique was used to separate and characterize the various forms of aluminum present in the prepared PAC solution. The effluents
from a gel column were monitored using online chemical method: Al-Ferron timed complexation spectrophotometry and by 27Al nuclear magnetic resonance (NMR) spectroscopy. Effects of different experimental conditions such as eluent flow rate, ionic
strength and pH on separation of Al13 were investigated. Experimental results indicated that molecule size exclusion was not the only parameter affecting the column
chromatographic separation efficiency of Al13 but molecule charge as well. Reducing the eluent flow rate, increasing the ionic strength and suitable pH resulted in increase
in the separation efficiency. Experimental results clearly indicated that by varying the experimental conditions, it is possible
to produce pure Al13 species using a gel column chromatographic technique. 相似文献
134.
Lukin O Müller WM Müller U Kaufmann A Schmidt C Leszczynski J Vögtle F 《Chemistry (Weinheim an der Bergstrasse, Germany)》2003,9(15):3507-3517
The readily available in gram quantities tris(allyloxy)knot of the amide-type 5 (knotane) can be completely and partially deprotected with nBu(3)SnH in the presence of a palladium catalyst resulting in hydroxyknotanes 7-9. These, in turn, react with diethylchlorophosphate giving rise to knotanes equipped with between one and three phosphoryl groups. Sulfonylation of bis(allyloxy)monohydroxyknotane 8 with p-toluenesulfonyl chloride and, following removal of one or two allyl groups from the intermediate monosulfonate 13, give rise to sulfonyloxy-allyloxy-hydroxy- and sulfonyloxy-dihydroxy-knotanes 15 and 14, respectively. This provides a convenient method for the preparation of knotanes with any substitution pattern. All new knotanes have been isolated in preparative amounts and as highly pure substances with an exception of allyloxy-dihydroxyknotane 9. This compound could only be obtained as a mixture with the corresponding monohydroxy-derivative 8. The structures of all synthesized compounds were established by means of FAB and MALDI TOF mass spectrometry, (1)H and (31)P NMR spectroscopy. The triphosphorylated knotane 10 exhibits high solubility in alcohols, allowing its complete enantiomeric resolution with a commercially available chiral HPLC column. (1)H,(1)H DQF-COSY correlation spectroscopy along with H/D exchange experiments and ab initio calculations provided the first detailed (1)H NMR signal assignments of knotanes in [D(6)]DMSO solution. The combination of variable temperature (1)H and (31)P NMR spectroscopy and molecular modeling has been applied to study the conformational behavior of the new knotanes in different solvents. It has been shown that in DMSO solution at room temperature knotanes exist in a relatively rigid nonsymmetrical conformation similar to that found in the solid state while faster conformational exchange leading to the average D(3) symmetrical structure was detected in a number of other solvents. 相似文献
135.
S. Thangavel 《Analytica chimica acta》2004,502(2):265-270
In situ distillation of borate ester into the curcumin solution has been developed for the spectrophotometric determination of boron in a variety of complex matrixes. A polypropylene vessel containing the sample solution was placed inside a vessel (PP) containing 10 ml of curcumin solution and the distillation was carried out at room temperature/on a water bath. The borate ester collected in to the curcumin solution was evaporated to dryness on the water bath, taken in acetone and the absorbance was measured at 550 nm. In situ distillation of borate ester directly into the chromogenic reagent eliminates tedious sample treatment (before and/or after borate separation), use of methanol, complicated quartz set up, possible loss of boron and reduces the analysis time significantly. In situ dehydration of sample solution by ethanolic vapour in the absence of dehydrating acid prevents the formation of fluoborate and co-distillation of potential anionic interferents (nitrate and fluoride). This developed method has been applied for the determination of traces of boric acid in boron powder by the distillation of methyl borate at room temperature. For other matrixes (water, uranium oxide, uranyl nitrate, fluoride salt, etc.) distillation of ethyl borate was carried out on the water bath. LOD (3σ) was 5 ng g−1 for water and 30 ng g−1 for solid samples. 相似文献
136.
By means of a vacuum time-lag method, gas transport properties of apolyimide based on 2, 2- bis (3, 4- decarboxyphenyl ) hexafluoropropane dianhydride (6FDA )and meta- phenylenediamine (mPDA ) have been measured as a function of upstream pres-sure and temperature. The results show that no gas-induced plasticization occurs for thispolyimide in the upstream pressure range from 1 atm to 20atm. The temperature depen-dence of P and D can be described by the Arrhenius equations. The activation energiesof permeation and diffusion were obtained for the gas/polymer pair studied and correlatedwith the size of penetrant gas. 相似文献
137.
138.
近年来,由于粒子填充聚合物共混物的广泛运用,复合材料的结构研究具有重要意义.除了研究粒子在聚合物中的分散外,关于粒子对聚合物共混物的相分离影响也做了大量工作.研究结果表明粒子的尺寸,粒子的表面处理以及粒子含量对聚合物共混物相分离热力学以及动力学有重要影响.由于粒子对聚合物组分的选择吸附、聚合物分子对粒子的润湿作用、填料对聚合物相区生长的阻碍导致了聚合物共混物-填料体系相行为的复杂性.本文扼要地综述了聚合物共混物-填料体系相分离的理论基础以及实验结果,介绍了粒子对相分离的影响因素,并展望了该领域的研究趋势和前景. 相似文献
139.
V. V. Nikitenko A. I. Martynenko S. A. Ostrovsky V. V. Rusak V. V. Kryuchkov D. A. Topchiev 《Russian Chemical Bulletin》1993,42(2):378-380
3-Methyl-l-vinylpyrazole (M3VP) and 5-methyl-1-vinylpyrazole (M5VP) were isolated as individual substances by vacuum rectification of their mixture (M3VP: M5VP 60 40). For each of them the kinetics of free-radical polymerization in MeOH were measured at low conversions. In both cases the rate of polymerization is proportional to 0.5 order with respect to the initiator (AIBN) concentration. On the other hand, a first order of reaction with respect to monomer concentration is observed only when the latter is relatively low (3M). At higher initial concentrations of monomers the order of reaction becomes less than unity. The overall rate of polymerization for M5VP was higher than for M3VP, whereas the initiation rate remained constant in the whole range of monomer concentrations and did not depend on the exact structure of the monomer. The difference in the rates of polymerization observed for M3VP and M5VP is probably connected with the difference in the key parameterk
p/k
t
1/2
for each of the two isomers. It is concluded that the correct kinetic information about homo- and co-polymerization of M3VP and M5VP cannot be obtained without their adequate separation.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 413–415, February, 1993. 相似文献
140.
高硅ZSM—5沸石填充硅橡胶膜的醇—水渗透蒸发分离性质 总被引:5,自引:3,他引:5
高硅ZSM-5沸石填充疏水性硅橡胶蓦地低浓度醇-水体度醇-水体的渗透蒸发性质的研究有明,提高沸石硅铝比,增加填充量以及进行酸处理皆有利于改善膜对醇-水的分离系数和通量。料液的成,浓度以及温度对膜的分离性质也有显著影响。 相似文献