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101.
Perfluorocarboxylic thioesters RFC(O)SR (RF=CF3(CF2)j, R=CH3(CH2)i, i andj=0–5) were studied for the first time by GLC on packed columns using SE-30, SKTFT-50X, and XE-60 as the stationary phase.
The values of thermodynamics functions of sorption were calculated. The correlations between these functions and the molecular
structures as well as the conditions of analysis were established. The insertion of the S atom into the molecules of derivatives
of perfluorocarboxylic acids causes a decrease in the contribution of the orientation interaction and an increase in the dispersion
interaction of thioesters with the stationary phases compared to esters and amides of perfluorocarboxylic acids studied previously.
For Part 1, see Ref. 1.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1165–1168, June, 1997. 相似文献
102.
103.
Arjan J. H. Louter Philo A. Jones J. David Jorritsma Jolan J. Vreuls Udo A. Th. Brinkman 《Journal of separation science》1997,20(7):363-368
An automated system for derivaatization was coupled on-line with solid-phase extraction-gas-chromatography (SPE-GC). The system was optimized for the determination of phenol and chlorinated phenols in aqueous samples. The test analytes were acetylated with acetic anhydride; proper buffering of the sample was a critical factor. Next, the phenol acetates were enriched on a SPE cartridge and transferred to a GC; two appraoaches were studied. In the first approach, the derivatives were enriched on disposable C18 cartridges (ASPEC type) and desorbed with methylacetate. Aan aliquot of the final eluate was injected on-line the GC by means of a loop-type interface. In the second approach, trace enrichment was performed on 10 × 2 mm i.d. LC-type precolumn packed with polystyrenedivinylbenzene copolymer (PLRP-S) this precolumn was dried with a mitrogen purge and the phenol acetates were desorbed with ethyl acetate which was injectedon-line into the retention gap of the GC under partially concurrent solvent evaporation (PCSE) conditions. The Derivatization-SPE-GC system which was based on the loop-type interface has the advantage of simplicity and easy operation, the main drawback is the impossibility to determine phenol acetates which elute prior to trichlorophenol acetates. With the derivatization-SPE-GC approach using PCSE-based desorption, even the most volatile analyte of the test series, phenol acetate, can be determined successfully. The entire procedure, including the derivatization step, was fully automated and integrated in one set-up. The precision data for the integrated on-line derivatization-SP-FID system were fully satisfactory, with RSD values of 1–12 % at the 1 μg/1 level. When a sample volume of 2.2 ml was analyzed, The detection limits for the chlorinated phenol acetates were in the 0.1–0.3 μg/1 range. 相似文献
104.
After describing simplified equations exspressing the temparature dependency of the viscosity of carrier gases (helium, nitrogen and hydrogen ) relative to a base value, absolute relationships based on the kinetic theory of gases are discussed. Comparative data obtained using various calculation methods are given and are compared to measured values. Based on the kinetic relationshipsm, of viscosity. Finally, the influence of pressure on the viscosity is also briefly discussed. As a supplement, Viscosity data are tabulated for the three gases in the range of 0°C to 400°C in increments of 2 K, calculated using the kinetic relationships. 相似文献
105.
本文提供一个求解重力和表面张力同时作用的周期前进二维非线性波的新方法.自由表面在计算域转入单位圆后用有限项Fourier级数表示.动力学边界条件用的是完整的非线性形式.Fourier级数的系数用Newton-Raphson方法迭代求解.这是一个精巧的方法.所用计算工作量小而结果精度高. 相似文献
106.
107.
Suzanne J. Dilly Steven J. Carlisle Andrew J. Clark Andrew R. Shepherd Stephen C. Smith Paul C. Taylor Andrew Marsh 《Journal of polymer science. Part A, Polymer chemistry》2006,44(7):2248-2259
A practical and divergent synthesis of supported [1,3,5]‐triazine dendritic molecules on Wang resin, PEGA resin, SynPhase? Lanterns, and silica gel is described. The alkylamine linkers used allow derivatization with functionality for both synthetic (e.g., supported reagent and scavenger activity) and chemical biology applications. The use of supported intermediates allows differentiation of symmetric linkers without the need for protecting group chemistry. The synthetic route uses inexpensive, readily available starting materials in a straightforward and scaleable strategy. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 2248–2259, 2006 相似文献
108.
109.
We report a simple TLC densitometric method for the quantification of hecogenin from the leaves of Agave americana using HPTLC. The method was validated for precision, repeatability and accuracy. The method was found to be precise with
RSD of 0.78 (intraday) and 0.82 (interday) for different concentrations of hecogenin. Instrumental precision was 0.42 (% RSD)
for hecogenin. The content of hecogenin in different samples was estimated by the proposed method and was found to be in the
range of 0.05−0.14% w/w in the samples analysed. Accuracy of the method was checked by conducting recovery study at three different levels for hecogenin
and the average percentage recovery was 98.98%, 101.92% and 103.33%, respectively. The TLC densitometric method developed
for the quantification of hecogenin was found to be simple, precise, specific, sensitive, accurate and can be used in routine
quality control.
Revised: 7 and 25 April 2006 相似文献
110.
用胶束液相色谱/安培检测器检测尿样中的扑热息痛及其主要水解产物4-氨基苯酚。采用14.5μm的碳纤维电极作为工作电极,以高于临界胶束浓度的阴离子表面活性剂十二烷基磺酸钠(SDS)作为液相色谱的流动相,尿样直接进样分析,扑热息痛和4-氨基苯酚的检测限分别为0.13nmol/L及0.73nmol/L(S/N=2)。 相似文献