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acetonitrile相关的网络例句

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与 acetonitrile 相关的网络例句 [注:此内容来源于网络,仅供参考]

Melamine is eluted from the SPE cartridge with 5% ammonium hydroxide / methanol, evaporated to dryness, reconstituted with internal standard and 50% acetonitrile / water, and analyzed by LC/MS/MS.

三聚氰胺使用5%的氢氧化铵/甲醇从SPE柱中洗脱,蒸发至干燥,用内标物与50%的乙腈/水重新配置成原来的浓度,通过LC/MS/MS分析。

The results indicate that the optimized sulfonylation reaction time is 4 h, the materiel rate of chlorosulfonic acid and 2-chloroimidazo[1,2-α]pyridine is 1.2 : 1, with ethylamine the yield increasing from 15.4% to above 70%; the optimized ammonolysis reaction time is 3 h and the reaction temperature is 27℃, with the acetonitrile yield increasing from 60.1% to above 79.6%.

实验结果表明,磺酰化反应的最佳反应时间为4 h,氯磺酸与2-氯咪唑并[1,-α]吡啶的用量比为1.2:1,加入三乙胺可将收率由15.4%提高到70%以上;氨解反应的最佳反应时间为3 h,反应温度为27 ℃,加入乙腈可将收率由60.1%提高到79.6%;方案经改进后,总反应时间缩短3 h,收率提高了5.5%。

This article mainly established the analysis method to extract the oxine-copper residues in cucumber and soil with ion pair of antiphase HPLC and Ultrasonic-assisted solvent. This method mainly uses XBridge C18 column and UV detector by using waters phase of phosphatic buffered solution/acetonitrile (60:40, by vol) as mobile phase with 0.8 mL/min flow ratio and UV detection at 250 nm. The residue time was 4.71 minute. Accuracy, precision, and sensitivity of the method all satisfy the demands of pesticide residue analysis.

建立了黄瓜和土壤中喹啉铜的超声波辅助溶剂提取-反相离子对高效液相色谱法的残留分析方法,该方法使用XBridge C18色谱柱和可变波长紫外检测器,并以水相磷酸盐缓冲溶液-乙腈(体积比为60:40)作流动相;流速为0.8 mL/min;检测波长为250 nm;保留时间为4.71 min;该方法的准确度、精密度及灵敏度均满足农药残留分析的要求。

The ultrasonic-assisted solvent extraction and quantitative analysis of the oxine-copper residues in soil with ion pair of antiphase HPLC was established. This methods mainly uses XBridge C5 column and UV detector by using waters phase of phosphatic buffered solution/acetonitrile (60:40, by vol) as mobile phase with 0.8 mL/min flow ratio and UV detection at 245 nm. The residue time was 4.72 minute. The linear correlation of this method was 0.9987. The recovery rate was 76.2 to 108.7%. Comparatively standard deviation was 0.6 to 3.37%. The detection limits of method was 0.05 mg/kg.

建立了土壤中喹啉铜的超声波辅助溶剂提取-反相离子对高效液相色谱法的残留分析方法,该方法使用XBridge C18色谱柱和可变波长紫外检测器,并以水相磷酸盐缓冲体系-乙腈(体积比60:40)作流动相;流速为0.8mL/min;检测波长为245nm;保留时间为4.72min;线性相关系数为0.9987,回收率在76.2%~108.7%之间,相对标准偏差在0.6%~3.37%之间,对土壤的最低检出限为0.05mg/kg。

The optimal separating condition of chromatography analysis was: Shimadzu VP-ODS 150mm4.6mm as chromatographic column; acetonitrile/water (12/88,V/V, Contained 1.25mmol/l phosphoric acid) as mobile phase with flow rate of 1.0ml/min. Macroporous ion exchange resins and activated carbon were applied to enrich the trace level impurities and the main impurities was determined by LC-MS and GC-MS.They were : Benzonitrile , 2-Methyl-8-hydroxyquinoline, 2,6-Pyridinediamine , O-ethyloxime Cyclo-hexanone and compound with 220 molecular weight .

采用离子树脂和活性炭吸附富集这些微量的杂质,并通过液质联用和气质联用对杂质进行了定性分析,鉴定了影响290nm吸收的主要杂质为苯甲腈,2甲基-8羟基喹啉,2,6二氨基吡啶,O-乙基环己酮肟和分子量220的物质。

The main contents are:(1) The polarized laser Raman spectra of acetone, methyl alcohol, alcohol, ethylene glycol, formamide, acetonitrile, acetic acid, Chloroform, Methylene chloride, and Bromoform are measured in the experiment.(2) The depolarization ratio of Raman shift in the measured spectrum are

主要的结果有:得到了丙酮分子9条喇曼谱线、甲醇分子5条喇曼谱线、乙醇分子9条喇曼谱线、乙二醇分子7条喇曼谱线、甲酰胺分子8条喇曼谱线、乙腈分子8条喇曼谱线、乙酸分子8条喇曼谱线

The ratios of mobile phase (methanol∶acetonitrile∶1% formic acid, pH3.0) were 10∶15∶75, 10∶10∶80, 6∶6∶88 for lettuce, celery and pakchoi cabbage, respectively.

生菜、芹菜和小白菜样品选用的流动相(甲醇∶乙腈∶1%甲酸,pH3.0)体积比分别为10∶15∶75,10∶10∶80,6∶6∶88。

The synthesized PU elastomer surface exhibited good affinity with acetonitrile and ethanol, and the corresponding advancing contact angles were examined to be less than 3 and 4 degrees, respectively.

首先使用低极性溶剂抽提,可以彻底清除基底表面硅烷的物理吸附层,然后逐渐提高抽提溶剂的极性,促使硅烷在扩散重组的过程中实现巯基的外向定位。

Methods: The analytical column was SHIMADZU VP-ODS C18 column(4.6 mm×150 mm, 5 μm) with a mobile phase consisted of 0.05 mol/L disodium hydrogen phosphate solution(85% phosphoric acid solution with pH adjustment to 2.5)-acetonitrile-methanol(42.5∶47.5∶10) at the flow rate of 1.0 ml/min, the detection wavelength was set at 254 nm.

色谱柱为SHIMADZU VP-ODS C18柱(4.6 mm×150 mm,5 μm),流动相为0.05 mol/L磷酸氢二钠溶液(用85%磷酸溶液调节pH值至2.5)-乙腈-甲醇(42.5∶47.5∶10),流速为1.0 ml/min,检测波长为254 nm。

Methods: The analytical column was SHIMADZU VP-ODS C18 column(4.6 mm×150 mm 5 μm) with a mobile phase consisted of 0.05 mol/L disodium hydrogen phosphate solution(85% phosphoric acid solution with pH adjustment to 2.5)-acetonitrile-methanol(42.5∶47.5∶10) at the flow rate of 1.0 ml/min the detection wavelength was set at 254 nm.

目的:建立丙酸氯倍他索尿素乳膏中丙酸氯倍他索含量的HPLC测定方法。方法:色谱柱为SHIMADZU VP-ODS C18柱(4.6 mm×150 mm5 μm)流动相为0.05 mol/L磷酸氢二钠溶液(用85%磷酸溶液调节pH值至2.5)-乙腈-甲醇(42.5∶47.5∶10)流速为1.0 ml/min 检测波长为254 nm。

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