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991.
992.
Yang Yan-Zhao Liu Wen-Tao Han Jian Zeng Shan Sun Si-Xiu 《Journal of Radioanalytical and Nuclear Chemistry》2004,260(3):647-651
The kinetics and mechanism of uranium(VI) extraction from nitric acid solution by bis(octylsulfinyl)methane (BOSM) are studied
with the method of stationary interface cell. The effects of temperature, extractant and nitric acid concentrations are discussed.
The results showed that the extraction process is controlled by the following reaction: UO2(NO3)2 + BOSM(i)⇄k1
k-1UO2(NO3)2BOSM(i). The variation of enthalpy associated with the extraction is -22.1±2.1 kJ/mol.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
993.
基于四苯硼钠与钾作用产生浊度 ,探讨并优化了流动注射分析条件 ,从而建立了测定人体体液中钾的新方法。方法简便、快速 ,每小时进样 6 0次 ,线性范围为 1.0× 10 - 4~ 1.0× 10 - 3mmol·ml- 1,所测尿样和血样的相对标准偏差分别为 3.0 8%和 2 .6 3%。 相似文献
994.
Elimination of matrix effects for headspace solid-phase microextraction of important volatile compounds in red wine using a novel coating 总被引:2,自引:0,他引:2
In this paper, hydroxy-terminated silicone oil-butyl methacrylate-divinylbenzene (OH-TSO-BMA-DVB) copolymer was first synthesized and used as stationary phase with the aid of γ-methacryloxypropyltrimethoxylsilane (KH-570) as bridge in solid-phase microextraction (SPME) using sol–gel method and cross-linking technique. It has high extraction efficiency for both polar alcohols and fatty acids and nonpolar esters in comparison with commercial PDMS, PDMS-DVB and PA fibers. A simple and sensitive headspace SPME-gas chromatography (HS-SPME-GC) method using the novel fiber was presented for the simultaneous analysis of both polar alcohols and fatty acids and nonpolar esters in wine. To check the matrix effects, various model wine matrices, including distilled water; 11.5% ethanol/water (v/v) solution; a concentrated synthetic wine; a ‘volatile-free’ wine and a real wine were investigated in detail. Matrix effects were compensated for by using internal standard method and selecting the ‘volatile-free’ wine as working standard. The method presented in this study showed satisfactory linearity, precision, detection limits and accuracy. The recoveries obtained ranged from 85.87 to 104.2%, and the relative standard deviation values were below 9%. The results obtained indicated that the present method is a validated and accurate procedure for the simultaneous determination of both polar and nonpolar aroma compounds in wine. 相似文献
995.
Jocelyn M. Bouzaid R. L. Frost W. N. Martens 《Journal of Thermal Analysis and Calorimetry》2007,89(2):511-519
The thermal stability and thermal decomposition pathways for synthesized composite iowaite/woodallite have been determined
using thermogravimetry analysis in conjunction with evolved gas mass spectrometry. Dehydration of the hydrotalcites occurred
over a range of 56–70°C. The first dehydroxylation step occurred at around 255°C and, with the substitution of more iron(III)
for chromium(III) this temperature increased to an upper limit of 312°C. This trend was observed throughout all decomposition
steps. The release of carbonate ions as carbon dioxide gas initialised at just above 300°C and was always accompanied by loss
of hydroxyl units as water molecules. The initial loss of the anion in this case the chloride ion was consistently observed
to occur at about 450°C with final traces evolved at 535 to 780°C depending of the Fe:Cr ratio and was detected as HCl (m/z=36). Thus for this to occur, hydroxyl units must have been retained in the structure at temperatures upwards of 750°C. Experimentally
it was found difficult to keep CO2 from reacting with the compounds and in this way the synthesized iowaite-woodallite series somewhat resembled the natural
minerals. 相似文献
996.
997.
998.
999.
J. Goworek W. Stefaniak Agnieszka Kierys Mariola Iwan 《Journal of Thermal Analysis and Calorimetry》2007,87(1):217-222
Mesoporous silica material of MCM-41 type was synthesized by co-condensation
of highly concentrated octyltriethoxysilane (OTEOS), octadecyltriethoxysilane
(ODTEOS) and tetraethoxysilane (TEOS). The obtained hybrid materials were
characterized using XRD, TG-DSC and low temperature adsorption/desorption
of nitrogen. It was shown that the applied method of synthesis allows to obtain
silica of MCM-41 type with a high degree of hydrocarbon saturation. 相似文献
1000.
Nanosized copolymer latex of hydroxypropylmethylcellulose (HPMC) grafted with ethyl acrylate (EA) and dimethylaminoethyl methacrylate
(DMAEMA) has been prepared by acidifying submicron-sized latex particles synthesized by soap-free emulsion graft copolymerization
using potassium persulfate (KPS) as initiator. The effects on the diameter of the latex particles of different conditions,
for example concentration of DMAEMA, amount of HPMC, and ratio of HCl to DMAEMA for acidification, were investigated. It was
found that increasing the mole ratio of HCl to DMAEMA to 1.0 and increasing the DMAEMA content both resulted in a decrease
in particle diameter, whereas increasing the amount of HPMC resulted in larger particle sizes. Measurement by dynamic light
scattering (DLS) revealed the diameter of the latex particles was >200 nm before acidification and <100 nm after acidification.
Evidence of grafting was obtained by use of Fourier transform infrared (FTIR) spectroscopy. Transmission electron microscopy
(TEM) was used to characterize the morphology of the copolymer particles before and after acidification. 相似文献