色谱
色譜
색보
CHINESE JOURNAL OF CHROMATOGRAPHY
2014年
3期
230-234
,共5页
陈潜%周宇艳%程欲晓%林苗
陳潛%週宇豔%程欲曉%林苗
진잠%주우염%정욕효%림묘
柱前衍生%高效液相色谱法%醛类化合物%2,4-二硝基苯肼%水性涂料
柱前衍生%高效液相色譜法%醛類化閤物%2,4-二硝基苯肼%水性塗料
주전연생%고효액상색보법%철류화합물%2,4-이초기분정%수성도료
pre-column derivatization%high performance liquid chromatography ( HPLC )%aldehydes%2,4-dinitrophenylhydrazine%water-based coatings
建立了柱前衍生高效液相色谱同时测定水性涂料中甲醛、乙醛、丙醛、苯甲醛、正戊醛和对甲基苯甲醛等6种醛类化合物的方法。样品经水超声提取后,与2,4-二硝基苯肼乙腈溶液在酸性条件下衍生,再经0.45μm 针式过滤器过滤后进样分析。系统考察了酸度调节剂、pH 值、反应温度、时间等因素对衍生反应的影响,优化的反应条件为:以稀释后的盐酸溶液作为酸度调节剂,缓冲溶液 pH =3,反应温度为60℃,反应时间为30 min。在此条件下,于0.08~2.0 mg / L 浓度范围内,6种醛类化合物呈良好的线性关系;检出限为0.05~2.50 mg / kg;在2.0、4.0、6.0 mg / kg 3个水平下的加标回收率为87.0%~112.8%;RSD 为1.12%~9.54%。结果表明,本方法具有较宽的线性范围,良好的精密度和准确度,适用于水性涂料中6种醛类化合物的同时测定。
建立瞭柱前衍生高效液相色譜同時測定水性塗料中甲醛、乙醛、丙醛、苯甲醛、正戊醛和對甲基苯甲醛等6種醛類化閤物的方法。樣品經水超聲提取後,與2,4-二硝基苯肼乙腈溶液在痠性條件下衍生,再經0.45μm 針式過濾器過濾後進樣分析。繫統攷察瞭痠度調節劑、pH 值、反應溫度、時間等因素對衍生反應的影響,優化的反應條件為:以稀釋後的鹽痠溶液作為痠度調節劑,緩遲溶液 pH =3,反應溫度為60℃,反應時間為30 min。在此條件下,于0.08~2.0 mg / L 濃度範圍內,6種醛類化閤物呈良好的線性關繫;檢齣限為0.05~2.50 mg / kg;在2.0、4.0、6.0 mg / kg 3箇水平下的加標迴收率為87.0%~112.8%;RSD 為1.12%~9.54%。結果錶明,本方法具有較寬的線性範圍,良好的精密度和準確度,適用于水性塗料中6種醛類化閤物的同時測定。
건립료주전연생고효액상색보동시측정수성도료중갑철、을철、병철、분갑철、정무철화대갑기분갑철등6충철류화합물적방법。양품경수초성제취후,여2,4-이초기분정을정용액재산성조건하연생,재경0.45μm 침식과려기과려후진양분석。계통고찰료산도조절제、pH 치、반응온도、시간등인소대연생반응적영향,우화적반응조건위:이희석후적염산용액작위산도조절제,완충용액 pH =3,반응온도위60℃,반응시간위30 min。재차조건하,우0.08~2.0 mg / L 농도범위내,6충철류화합물정량호적선성관계;검출한위0.05~2.50 mg / kg;재2.0、4.0、6.0 mg / kg 3개수평하적가표회수솔위87.0%~112.8%;RSD 위1.12%~9.54%。결과표명,본방법구유교관적선성범위,량호적정밀도화준학도,괄용우수성도료중6충철류화합물적동시측정。
A high performance liquid chromatography method with pre-column derivatization was developed for the simultaneous determination of formaldehyde,acetaldehyde,propionalde-hyde,benzaldehyde,n-valeraldehyde and p-tolualdehyde in water-based coatings. After ultra-sonic extraction with water, the samples were derivatized with 2,4-dinitrophenylhydrazine (2,4-DNPH)in acetonitrile under acidic condition,then filtrated by 0. 45 μm organic syringe filters for the determination. Systematic investigation was carried out on the dependence of the derivatization conditions such as the acidity regulator,pH value,reaction temperature,reaction time and other factors. The optimized conditions were as follows:the dilute hydrochloric acid solution as acidity regulator,the pH of the buffer solution of 3,the reaction temperature of 60℃ ,and the reaction time of 30 min. Under the conditions,a linear relation was achieved in the range of 0. 08-2. 0 mg / L for the peak area to concentration of the six aldehydes. The detection limits were 0. 05-2. 50 mg / kg. The recoveries of standard addition at the spiked levels of 2. 0, 4. 0,6. 0 mg / kg were 87. 0% - 112. 8% with the relative standard deviations( RSDs,n = 6)of 1. 12% -9. 54% . The results showed that this method has a wide linear range,good precision and accuracy,and it is suitable for the simultaneous determination of the six aldehydes in water-based coatings.