Gas chromatographic determination of silicon fluoride-chlorides SiСlnF4-n (n = 0 ÷ 4) obtained by the reaction of silicon tetrafluoride with aluminum chloride (III)

Q4 Chemistry Analitika i Kontrol Pub Date : 2019-12-18 DOI:10.15826/analitika.2019.23.4.011
Т. G. Sorochkina, О. Y. Chernova, О. Y. Troshin, А. Y. Sozin, А. Bulanov, А. А. Ermakov
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引用次数: 1

Abstract

It is for the first time that the method of gas chromatography was used for the determination of silicon fluoride-chlorides SiСl n F 4-n ( n = 0 ÷ 4) which are the initial, intermediate and final substances while producing silicon tetrachloride from silicon tetrachloride and aluminum chloride (III). The analysis of samples taken during this reaction was carried out using the "Tsvet - 800" gas chromatographer. The samples were injected into the instrument using a vacuum dosing system. To separate the components, a chromatographic column made of molybdenum glass with a length of 5 m and an internal diameter of 3 mm was used. It was filled with a Chromatone N-AW-HMDS (grain size 0.250-0.315 mm) with 15% methylsilicon elastoplastic E-301. The registration of silicon fluoride-chlorides was implemented using a thermal conductivity detector. The identification of SiF 4 and SiCl 4 in the mixture was conducted by comparing the times of holding the chromatographic peaks with the times of holding these individual substances. The times of holding not available for SiClF 3 , SiCl 2 F 2 , SiCl 3 F in the individual states were determined using the dependence of the logarithm of the corrected holding time on their molecular mass. The concentrations of silicon fluoride-chlorides were determined using the internal normalization method. The data were obtained on the changes in the concentrations of these substances during the synthesis of silicon tetrachloride. The confirmation of the correctness of the analysis results was made using the method of varying the size of the sample. Key words:  silicon fluoride-chlorides, gas chromatography, identification, calibration factor, correctness (Russian)  DOI: http://dx.doi.org/10.15826/analitika.2019.23.4.011 Т .G. Sorochkina, О .Yu. Chernova, О .Yu. Troshin, А .Yu. Sozin, А .D. Bulanov, А . А . Ermakov G.G. Devyatykh Institute of Chemistry of High-Purity Substances of the Russian Academy of Sciences, ul. Tropinina 49, Nizhny Novgorod, 603950, Russian Federation
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气相色谱法测定四氟化硅与氯化铝(III)反应得到的氟化硅-氯化物SiСlnF4-n (n = 0 ÷ 4)
首次采用气相色谱法测定由四氯化硅和氯化铝(III)生产四氯化硅时的初始、中间和最终物质氟化硅氯化物SiСl n F 4-n(n=0÷4)。使用“Tsvet-800”气相色谱仪对反应过程中采集的样品进行分析。使用真空给药系统将样品注入仪器中。为了分离组分,使用长度为5m、内径为3mm的钼玻璃制成的色谱柱。用具有15%甲基硅弹塑性E-301的Chromatone N-AW-HMDS(粒度0.250-0.315 mm)填充。氟化硅氯化物的登记是使用热导率检测器来实现的。混合物中SiF4和SiCl4的鉴定是通过将色谱峰的保持时间与这些单独物质的保持时间进行比较来进行的。SiClF3、SiCl2F2、SiCl3F在各个状态下不可用的保温时间是通过校正保温时间的对数对其分子质量的依赖性来确定的。氟化硅氯化物的浓度是通过内部归一化方法确定的。获得了四氯化硅合成过程中这些物质浓度变化的数据。采用改变样品大小的方法对分析结果的正确性进行了确认。关键词:氟化硅氯化物,气相色谱法,鉴定,校准因子,正确性(俄语)DOI:http://dx.doi.org/10.15826/analitika.2019.23.4.011Т.G.Sorochkina,О.Yu.Chernova,О.Yu.Troshin,А.Yu.Sozin,А.D.Bulanov,А。А。Ermakov G.G.Devyatykh俄罗斯科学院高纯物质化学研究所,ul。Tropinina 49,下诺夫哥罗德,603950,俄罗斯联邦
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来源期刊
Analitika i Kontrol
Analitika i Kontrol Chemistry-Analytical Chemistry
CiteScore
0.90
自引率
0.00%
发文量
15
期刊介绍: Analitika i Kontrol is a scientific journal covering theoretical and applied aspects of analytical chemistry and analytical control, published since autumn 1997. Founder and publisher of the journal is the Ural Federal University named after the first President of Russia Boris Yeltsin (UrFU, Ekaterinburg).
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