色谱
色譜
색보
CHINESE JOURNAL OF CHROMATOGRAPHY
2014年
6期
662-665
,共4页
赵彦%徐董育%林浩学%陈晓燕%陈泽勇
趙彥%徐董育%林浩學%陳曉燕%陳澤勇
조언%서동육%림호학%진효연%진택용
二维气相色谱%乙酸乙酯%乙酸仲丁酯%碳酸二甲酯%汽油
二維氣相色譜%乙痠乙酯%乙痠仲丁酯%碳痠二甲酯%汽油
이유기상색보%을산을지%을산중정지%탄산이갑지%기유
two-dimensional gas chromatography%ethyl acetate%sec-butyl acetate%dimethyl carbonate%gasoline
建立了一种采用填充柱切割-反吹二维气相色谱分析汽油中酯类化合物(包括乙酸乙酯、乙酸仲丁酯、碳酸二甲酯)的方法。利用非极性填充预柱将汽油中沸点低于正辛烷的轻组分保留进入分析柱,重组分反吹放空,轻组分和酯类化合物经一个装填有强极性固定相的色谱柱分离分析。采用外标法定量,3种酯类化合物在50~50000 mg / L 范围内线性关系良好,相关系数(r2)分别为0.99999、1.00000和0.99995,标准样品6次重复性测定的相对标准偏差(RSD)均小于1.0%,回收率在98.7%~107.9%之间,方法检出限( S / N =3)为5 mg / L。该方法不需要进行样品前处理,具有操作简单,准确高效的特点,是汽油中酯类化合物测定的理想分析方法。
建立瞭一種採用填充柱切割-反吹二維氣相色譜分析汽油中酯類化閤物(包括乙痠乙酯、乙痠仲丁酯、碳痠二甲酯)的方法。利用非極性填充預柱將汽油中沸點低于正辛烷的輕組分保留進入分析柱,重組分反吹放空,輕組分和酯類化閤物經一箇裝填有彊極性固定相的色譜柱分離分析。採用外標法定量,3種酯類化閤物在50~50000 mg / L 範圍內線性關繫良好,相關繫數(r2)分彆為0.99999、1.00000和0.99995,標準樣品6次重複性測定的相對標準偏差(RSD)均小于1.0%,迴收率在98.7%~107.9%之間,方法檢齣限( S / N =3)為5 mg / L。該方法不需要進行樣品前處理,具有操作簡單,準確高效的特點,是汽油中酯類化閤物測定的理想分析方法。
건립료일충채용전충주절할-반취이유기상색보분석기유중지류화합물(포괄을산을지、을산중정지、탄산이갑지)적방법。이용비겁성전충예주장기유중비점저우정신완적경조분보류진입분석주,중조분반취방공,경조분화지류화합물경일개장전유강겁성고정상적색보주분리분석。채용외표법정량,3충지류화합물재50~50000 mg / L 범위내선성관계량호,상관계수(r2)분별위0.99999、1.00000화0.99995,표준양품6차중복성측정적상대표준편차(RSD)균소우1.0%,회수솔재98.7%~107.9%지간,방법검출한( S / N =3)위5 mg / L。해방법불수요진행양품전처리,구유조작간단,준학고효적특점,시기유중지류화합물측정적이상분석방법。
A simple and efficient method based on the technique of packed column switching-back flushing was established for the analysis of the ester compounds(including ethyl acetate, sec-butyl acetate,dimethyl carbonate)in gasoline. With the use of a non-polar pre-column,we successfully separated the components in gasoline by back flushing out components heavier than n-octane,while the lighter components and the ester compounds were flushed into a polar analytical column. In this method,external standard method was applied for quantification. As a result,good linear relationships existed among the three ester compounds in the range of 50 mg / L to 50 000 mg / L. The linear correlation coefficients( r 2 )for ethyl acetate,sec-butyl ace-tate and dimethyl carbonate were 0. 999 99,1. 000 00 and 0. 999 95,respectively. The relative standard deviations(RSDs)of standard samples in six continuous tests were within 1. 0% . The recoveries were between 98. 7% and 107. 9% . The detection limit of the method(S / N = 3)was 5 mg / L. No pretreatment was needed. This method is simple,accurate,quick as well as effi-cient,and can be used as an ideal method for the analysis of the ester compounds in gasoline.