岩矿测试
巖礦測試
암광측시
ROCK AND MINERAL ANALYSIS
2001年
1期
20-22
,共3页
王俊奇%史向阳%张松伟%林玉侠%杨光伟%马万云%陈瓞延
王俊奇%史嚮暘%張鬆偉%林玉俠%楊光偉%馬萬雲%陳瓞延
왕준기%사향양%장송위%림옥협%양광위%마만운%진질연
胶束电动毛细管色谱法%海底表层沉积物%苯系化合物
膠束電動毛細管色譜法%海底錶層沉積物%苯繫化閤物
효속전동모세관색보법%해저표층침적물%분계화합물
用胶束电动毛细管色谱法对海底表层沉积物中的苯系化合物进行了分析测定。采用57cm×50μm毛细管柱,以50mmol/L十二烷基硫酸钠-2.0mmol/L四硼酸钠溶液(pH9.16)作为操作缓冲溶液,并加入φ=20%的甲醇作为有机改性剂,电压25kV,检测波长200nm,15min内苯、甲苯、乙苯和二甲苯可获得良好的分离。用峰面积定量,线性范围为2~100mg/L,最小检测浓度分别为0.75mg/L苯,0.45mg/L甲苯,0.39mg/L乙苯,0.1mg/L邻-二甲苯,0.31mg/L对-二甲苯。将该法用来分析石油勘探远景区域海底表层沉积物中的苯系化合物,检测浓度范围为(0.0x~0.x)μg/g。
用膠束電動毛細管色譜法對海底錶層沉積物中的苯繫化閤物進行瞭分析測定。採用57cm×50μm毛細管柱,以50mmol/L十二烷基硫痠鈉-2.0mmol/L四硼痠鈉溶液(pH9.16)作為操作緩遲溶液,併加入φ=20%的甲醇作為有機改性劑,電壓25kV,檢測波長200nm,15min內苯、甲苯、乙苯和二甲苯可穫得良好的分離。用峰麵積定量,線性範圍為2~100mg/L,最小檢測濃度分彆為0.75mg/L苯,0.45mg/L甲苯,0.39mg/L乙苯,0.1mg/L鄰-二甲苯,0.31mg/L對-二甲苯。將該法用來分析石油勘探遠景區域海底錶層沉積物中的苯繫化閤物,檢測濃度範圍為(0.0x~0.x)μg/g。
용효속전동모세관색보법대해저표층침적물중적분계화합물진행료분석측정。채용57cm×50μm모세관주,이50mmol/L십이완기류산납-2.0mmol/L사붕산납용액(pH9.16)작위조작완충용액,병가입φ=20%적갑순작위유궤개성제,전압25kV,검측파장200nm,15min내분、갑분、을분화이갑분가획득량호적분리。용봉면적정량,선성범위위2~100mg/L,최소검측농도분별위0.75mg/L분,0.45mg/L갑분,0.39mg/L을분,0.1mg/L린-이갑분,0.31mg/L대-이갑분。장해법용래분석석유감탐원경구역해저표층침적물중적분계화합물,검측농도범위위(0.0x~0.x)μg/g。
A method was developed using micellar electrokinetic capillary chromatography (MECC) to analyze and determine the content of the benzene homologue compounds in marine shallow sediment samples. A fused silica capillary of 57cm×50μm (50cm to detector) was used. Running buffer was 2.0 mmol/L aqueous tetraborate solution containing 50mmol/L sodium dodecyl sulfate (pH 9.16) and 20% methanol as an organic modifier. The voltage used was 25 kV. Detection wavelength was 200nm.Benzene, toluene, ethylbenzene and xylene were separated well within 15min.Peak area was measared for quantitative analysis. The calibration curves were linear over 2~100mg/L. The minimum detectable concentrations were 0.75mg/L for benzene, 0.45mg/L for toluene, 0.39mg/L for ethylbenzene, 0.1mg/L for o-xylene and 0.31mg/L for p-xylene. Benzene homologue compounds in marine shallow sediment samples, which deposit in the prospect area of oil exploration, were analyzed using proposed method. The detection ranges obtained for these compounds were (0.0x~0.x)μg/g.