藥典乙醇填充柱標(biāo)準(zhǔn)，液化石油氣，二甲醚，甲縮醛，乙縮醛，乙醇，室內(nèi)空氣，焦?fàn)t煤氣，煉廠氣，天然氣，變壓器油，多氯聯(lián)苯，植物油，6號(hào)溶劑殘留，裂解進(jìn)樣器，消毒劑，氨水

藥典乙醇填充柱標(biāo)準(zhǔn)
藥典乙醇填充柱標(biāo)準(zhǔn) 詳細(xì)信息：

     色譜條件與系統(tǒng)適用性試驗(yàn) 用直徑為0.18～0.25mm 的二乙烯苯-乙基乙烯苯型高分子多孔小球作為載體，柱溫為120～150℃。理論板數(shù)按正丙醇峰計(jì)算應(yīng)不低于700，乙醇峰與正丙醇峰的分離度應(yīng)大于2.0。
    校正因子測定 精密量取恒溫20℃的無水乙醇4ml、5ml、6ml，分別置100ml量瓶中，分別精密加入恒溫20℃的正丙醇（內(nèi)標(biāo)物質(zhì)）5ml，用水稀釋刻度，搖勻（必要時(shí)可進(jìn)一步稀釋）。取上述三種溶液各適量，注入氣相色譜儀，分別連續(xù)進(jìn)樣3次，測定峰面積，計(jì)算校正因子，所得校正因子的相對標(biāo)準(zhǔn)偏差不得大于2.0%。
    測定法 精密量取恒溫20℃的供試品溶液適量（相當(dāng)于乙醇約5ml），置100ml量瓶中，精密加入恒溫20℃的正丙醇5ml，用水稀釋刻度，搖勻（必要時(shí)可進(jìn)一步稀釋），取適量注入氣相色譜儀，測定峰面積，按內(nèi)標(biāo)法以峰面積計(jì)算，即得。
    【附注】（1）在不含內(nèi)標(biāo)物質(zhì)的供試品溶液的色譜圖中，與內(nèi)標(biāo)物質(zhì)峰相應(yīng)的位置處不得出現(xiàn)雜質(zhì)峰。
    （2）除另有規(guī)定外，若蒸餾法測定結(jié)果與氣相色譜法不一致，以氣相色譜法測定結(jié)果為準(zhǔn)。

名稱：填充柱

規(guī)格：2m*1/8

型號(hào)：GDX-102

應(yīng)用：藥典乙醇測定

藥典乙醇填充柱標(biāo)準(zhǔn)  圖片：



Pharmacopoeia ethanol packed column standard
Pharmacopoeia ethanol packed column standard Details:

     Chromatographic conditions and system suitability test Use divinylbenzene-ethylvinylbenzene type polymer porous beads with a diameter of 0.18～0.25mm as the carrier, and the column temperature is 120～150℃. The number of theoretical plates calculated based on the n-propanol peak should not be less than 700, and the resolution between the ethanol peak and the n-propanol peak should be greater than 2.0.
    Calibration factor determination. Precisely measure 4ml, 5ml, and 6ml of absolute ethanol at a constant temperature of 20°C, put them into a 100ml measuring flask, respectively, accurately add 5ml of n-propanol (internal standard substance) at a constant temperature of 20°C, and dilute to the mark with water. Shake well (dilute further if necessary). Take appropriate amounts of each of the above three solutions and inject them into the gas chromatograph, respectively, inject three consecutive samples, measure the peak area, and calculate the correction factor. The relative standard deviation of the obtained correction factor shall not be greater than 2.0%.
    Determination method Precisely measure an appropriate amount of the test solution at a constant temperature of 20°C (equivalent to about 5ml of ethanol), put it in a 100ml measuring flask, and accurately add 5ml of n-propanol at a constant temperature of 20°C, dilute to the mark with water, and shake well (necessary It can be further diluted), take an appropriate amount into the gas chromatograph, measure the peak area, and calculate the peak area according to the internal standard method to obtain.
    [Note] (1) In the chromatogram of the test solution containing no internal standard substance, no impurity peak should appear at the position corresponding to the peak of the internal standard substance.
    (2) Unless otherwise specified, if the result of the distillation method is inconsistent with the gas chromatography method, the gas chromatography method shall prevail.

Name: Packed column

Specification: 2m*1/8

Model: GDX-102

Application: Pharmacopoeia ethanol determination




Pharmacopoeia ethanol packed column standard Picture: