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ANALYTICAL INSTRUMENTATION
2014年
3期
34-39
,共6页
额日和木%王旭%张煜琳%萨嘎拉%照日格图
額日和木%王旭%張煜琳%薩嘎拉%照日格圖
액일화목%왕욱%장욱림%살알랍%조일격도
苯%苯酚%内标法%外标法%高效液相色谱
苯%苯酚%內標法%外標法%高效液相色譜
분%분분%내표법%외표법%고효액상색보
benzene%phenol%internal standard method%external standard method%high performance liquid chromatography
本文采用高效液相色谱法,以乙腈-水(50:50,v/v)混合溶液为流动相,经 YMC -C18(250 mm ×46mm ,5μm)色谱柱分离,紫外检测波长为270nm时,测定了苯、苯酚、对苯醌、邻苯二酚、间苯二酚、对苯二酚和苯三酚。结果表明:苯、苯酚、对苯醌、邻苯二酚、间苯二酚、对苯二酚和苯三酚在各自的测定范围内均有良好的线性关系(相关系数为≥0.999),方法的检出限为0.002~0.008μg/mL。内标法(ISM )回收率为80.40%~101.59%,相对标准偏差<9.6%;外标法(ESM )回收率为82.72%~99.48%,相对标准偏差<10.8%。说明在苯、苯酚、对苯醌、邻苯二酚、间苯二酚、对苯二酚和苯三酚定量分析方法中内标法优于外标法,并且该方法操作简便、快速、稳定性好、样品和溶液用量少,分析条件温和。
本文採用高效液相色譜法,以乙腈-水(50:50,v/v)混閤溶液為流動相,經 YMC -C18(250 mm ×46mm ,5μm)色譜柱分離,紫外檢測波長為270nm時,測定瞭苯、苯酚、對苯醌、鄰苯二酚、間苯二酚、對苯二酚和苯三酚。結果錶明:苯、苯酚、對苯醌、鄰苯二酚、間苯二酚、對苯二酚和苯三酚在各自的測定範圍內均有良好的線性關繫(相關繫數為≥0.999),方法的檢齣限為0.002~0.008μg/mL。內標法(ISM )迴收率為80.40%~101.59%,相對標準偏差<9.6%;外標法(ESM )迴收率為82.72%~99.48%,相對標準偏差<10.8%。說明在苯、苯酚、對苯醌、鄰苯二酚、間苯二酚、對苯二酚和苯三酚定量分析方法中內標法優于外標法,併且該方法操作簡便、快速、穩定性好、樣品和溶液用量少,分析條件溫和。
본문채용고효액상색보법,이을정-수(50:50,v/v)혼합용액위류동상,경 YMC -C18(250 mm ×46mm ,5μm)색보주분리,자외검측파장위270nm시,측정료분、분분、대분곤、린분이분、간분이분、대분이분화분삼분。결과표명:분、분분、대분곤、린분이분、간분이분、대분이분화분삼분재각자적측정범위내균유량호적선성관계(상관계수위≥0.999),방법적검출한위0.002~0.008μg/mL。내표법(ISM )회수솔위80.40%~101.59%,상대표준편차<9.6%;외표법(ESM )회수솔위82.72%~99.48%,상대표준편차<10.8%。설명재분、분분、대분곤、린분이분、간분이분、대분이분화분삼분정량분석방법중내표법우우외표법,병차해방법조작간편、쾌속、은정성호、양품화용액용량소,분석조건온화。
Based on the high performance liquid chromatography method ,benzene and its direct oxida-tion products :phenol , benzoquinone , o-Bihydroxybenzene , m-Bihydroxybenzene , p-Bihydroxybenzene , benzenetriol were completely separated by the YMC-C18(250mm × 46mm ,5μm) chromatographic column with acetonitrile-water(50:50 ,v/v) as mobile phase .The UV detection wavelength was set at 270 nm .The result showed good linearity (R≥0 .99) ,the detection limit of the samples were between 0 .002-0 .008 μg/mL .The recoveries of internal standard method(ISM) ranged from 80 .40 to 101 .59% at the three spiked levels ,the relative standard deviation was below 9 .6% ;the recoveries of external standard method (ESM ) ranged from 82 .72 to 99 .48% at three spiked levels ,the relative standard deviation was below 10 .8% .It was indicated that the internal standard method was better than the external standard method for the quan-titative analysis of benzene and its products of oxidation .T his method is simple ,rapid ,sensitive and stabi-lized ,low consumption of sample and solution ,and analytical conditions are moderate .