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顶空气相色谱法结合电解电导检测法测定脱咖啡因茶和咖啡中的二氯甲烷。

Headspace gas chromatographic determination of methylene chloride in decaffeinated tea and coffee, with electrolytic conductivity detection.

作者信息

Page B D, Charbonneau C F

出版信息

J Assoc Off Anal Chem. 1984 Jul-Aug;67(4):757-61.

PMID:6469909
Abstract

A headspace gas chromatographic procedure is described for the determination of methylene chloride (MC) in decaffeinated tea and coffee. The tea or coffee sample, with added methylene bromide (MB) internal standard, is equilibrated for 1.5 h at 100 degrees C in aqueous sodium sulfate before manual headspace sampling. MC and MB are separated on a Porasil A column at 160 degrees C and detected by using a Coulson electrolytic conductivity detector. For coffee and tea samples spiked at 1.3 ppm MC, as well as commercially decaffeinated teas and coffees containing up to 8 ppm MC, coefficients of variation were 10% or less. For decaffeinated teas, problems involving sample homogeneity and loss of MC before sealing the headspace vial had to be overcome. Similar problems with decaffeinated instant and ground coffees were minimal. The headspace procedure was superior to a previously reported distillation technique. MC was readily detected at 0.05 ppm. Fourteen decaffeinated teas and 15 decaffeinated coffees were analyzed; MC was detected at levels that ranged up to 15.9 and 4.0 ppm, respectively.

摘要

描述了一种顶空气相色谱法,用于测定脱咖啡因茶和咖啡中的二氯甲烷(MC)。将添加了二溴甲烷(MB)内标的茶或咖啡样品,在100℃的硫酸钠水溶液中平衡1.5小时,然后进行手动顶空进样。MC和MB在160℃的Porasil A柱上分离,并用库尔森电解电导检测器检测。对于添加了1.3 ppm MC的咖啡和茶样品,以及含有高达8 ppm MC的市售脱咖啡因茶和咖啡,变异系数为10%或更低。对于脱咖啡因茶,必须克服样品均匀性和在密封顶空瓶之前MC损失的问题。脱咖啡因速溶咖啡和研磨咖啡的类似问题很少。顶空法优于先前报道的蒸馏技术。在0.05 ppm时很容易检测到MC。分析了14种脱咖啡因茶和15种脱咖啡因咖啡;检测到的MC含量分别高达15.9和4.0 ppm。

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