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981.
V. V. Barbakadze E. P. Kemertelidze I. Targamadze K. Mulkidzhanyan J. Kemink A. J. J. van den Berg K. J. Beukelman A. I. Usov 《Chemistry of Natural Compounds》2005,41(4):374-377
Two high-molecular-weight (>1000 kDa) water-soluble preparations were isolated from stems of Symphytum asperum and S. caucasicum. Their basic component was established as poly[hydroxy-1-carboxy-2-(3,4-dihydroxyphenyl)ethylene], analogous to that of high-molecular-weight
(>1000 kDa) preparations from roots of these same plants, using IR and NMR spectral data.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 303–305, July–August, 2005.
An erratum to this article is available at . 相似文献
982.
Ronald K. Mitchum Walter A. Korfmacher James R. Althaus 《Journal of mass spectrometry : JMS》1984,19(2):63-66
The high toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin (2,3,7,8-TCDD) has led to the development of selective and highly sensitive quantitative methods for mass spectral analysis. Analytical selectivity has been demonstrated for the oxygen negative chemical ionization (ONCI) reaction of TCDD in an oxygen-rich plasma. While the reaction product (4,5-dichloro-1,2-benzoquinone anion) of 2,3,7,8-TCDD and oxygen is well known, the mechanism of its formation has not been studied thoroughly. In this report the results of a study involving the reaction of 18O2 with 2,3,7,8-TCDD under high pressure and low pressure ONCI conditions are reported. A mechanism is proposed which is compatible with the observation that one 18O atom is incorporated into the product anion. 相似文献
983.
Stephen de Mora Jean-Pierre Villeneuve Eric Wyse 《Accreditation and quality assurance》2007,12(11):587-592
Aspects of the International Atomic Energy Agency (IAEA) Analytical Quality Control Services (AQCS) for marine environmental
studies are discussed, focusing on recent laboratory performance studies (LPS) and the production of reference materials for
trace metals and organic compounds in various marine matrices. The IAEA has organized seventeen global interlaboratory studies
for a range of organic contaminants. Of note has been the inclusion of numerous polychlorinated biphenyl congeners (PCBs)
and some sterols of anthropogenic origin. Concurrently, there have been eleven worldwide intercomparison exercises for trace
metals in the marine environment, most of which included methylmercury. Although such interlaboratory studies can help improve
performance in individual laboratories and regional laboratory networks, the results reveal that problems remain in the determination
of some metals and many organic contaminants. 相似文献
984.
Summary. An efficient direct conversion of THP ethers into the corresponding acetates was achieved with acetic anhydride in the presence of CuSO4 · 5H2O as an available and green catalyst in high yields. 相似文献
985.
986.
The use of fenugreek mucilage, a natural polysaccharide and a direct food additive, as a flocculating agent for removal of suspended and dissolved solids from sewage effluent has been reported. A flocculation study has been done by the standard jar test method. The percent removal of suspended solid (SS) and dissolved solid (TDS) was determined by varying the polymer dose, pH and contact time. X-ray diffraction patterns of the solid waste material of mucilage and flocs (so obtained after treatment) were used to suggest the incorporation of the crystalline waste material in the mucilage. The optimal mucilage concentration was found to be 0.16 mg/l. The suitable pH range for maximum solid removal (SS and TDS) was alkaline and the time required for treatment was 1-3 h. 相似文献
987.
In the EURACHEM/CITAC draft ”Quantifying uncertainty in analytical measurement” estimations of measurement uncertainty in
analytical results for linear calibration are given. In this work these estimations are compared, i.e. the uncertainty deduced
from repeated observations of the sample vs. the uncertainty deduced from the standard residual deviation of the regression.
As a result of this study it is shown that an uncertainty estimation based on repeated observations can give more realistic
values if the condition of variance homogeneity is not correctly fulfilled in the calibration range. The complete calculation
of measurement uncertainty including assessment of trueness is represented by an example concerning the determination of zinc
in sediment samples using ICP-atomic emission spectrometry.
Received: 9 February 2002 Accepted: 17 April 2002 相似文献
988.
Aamer Saeed 《Chemistry of Heterocyclic Compounds》2007,43(8):1072-1075
An efficient, rapid, microwave-accelerated one-step synthesis of some 5-aryl-2-(2-hydroxy-phenyl)-1,3,4-oxadiazoles by reaction
of salicylic hydrazide with carboxylic acids in the presence of thionyl chloride under neat conditions is described.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1264–1267, August, 2007. 相似文献
989.
Analysis of methyl- and ethylmercury (MM and EM) halides in biological and environmental samples is generally performed by gas chromatography with electron capture detection. Tedious sample work-up protocols and poor chromatographic response (using packed columns) have, however, shown the need for the development of new methods in this field. This paper reports a sensitive method, free from these deficiencies, for the determination of methyl- and ethylmercury. The organomercury compounds (MM and EM) are first released from the sample matrix, by the combined action of acidic potassium bromide and cupric ions, and then extracted into dichloromethane. The initial extracts are subjected to thiosulfate clean-up and the organomercury species are isolated as their chloride derivatives by addition of cupric chloride, and subsequent extraction into a small volume of organic solvent. Capillary GC coupled with atomic fluorescence detection provided excellent separation efficiencies for methyl- and ethylmercury and proved to be a very selective and sensitive technique. The absolute detection limit for both MM and EM was found to be 0.2 pg. 相似文献
990.
Daniel S. Trifan Ronald A. Shelden John J. Hoglen 《Journal of polymer science. Part A, Polymer chemistry》1968,6(6):1605-1614
1, 4-Pentadiene has been polymerized by Ziegler-Natta catalysts to give amorphous polymers which are up to 64 wt.-% soluble. The polymers all have residual unsaturation which is substantially less than one double bond per mer, some as low as 0.1 double bond per mer. The polymerizations proceed by an unusual double inter-, double intramolecular cyclopolymerization mechanism leading to the formation of [3.3.1] bicyclic repeat units. Some main-chain (internal) unsaturation as well as pendant-group (external) unsaturation is observed. The latter results from incompletely cyclized 1,4-pentadiene units. The former is due to some concurrent isomerization of 1,4- to 1,3 pentadiene, which then copolymerizes with the 1,4 diene. The extent of isomerization varied with the catalyst system used. The soluble polymer fractions were brittle for internal unsaturations of less than about 0.05 double bond per mer and were viscous for higher values. The insoluble fractions were brittle and are believed to be lightly crosslinked. 相似文献