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作 者:于修烛[1] 杜双奎[1] 李志西[1] 张静亚[1]
机构地区:[1]西北农林科技大学食品科学与工程学院,陕西杨凌712100
出 处:《中国食品学报》2011年第7期169-175,共7页Journal of Chinese Institute Of Food Science and Technology
基 金:中央高校基本科研业务费专项资金资助(QN2009074)
摘 要:以食用油、三苯磷、三苯氧磷和矿物精油为试验材料,基于氢过氧化物与三苯磷(TPP)快速反应生成三苯基氧磷(TPPO)及其在红外光谱542cm-1处有特征吸收的原理,采用FTIR光谱重组检测(SR-FTIR)技术对食用油的过氧化值进行建模及模型验证分析。结果表明:TPPO浓度(以相应的过氧化值表示)与542cm-1处吸收强度(相对基线位于530cm-1)之间高度线性相关,相关系数为0.9999,标准差为0.067mmol/kg。对2个验证样品集(0~1.5mmol/kg和1.5~10mmol/kg)进行测定并与碘量法比较,SR-FTIR技术的灵敏度和精度均高于碘量法。通过自动分析仪SR-FTIR测定过氧化值的分析速度可达每小时90个样品。The paper took edible oils,triphenylphosphine(TPP),triphenylphosphine oxide(TPPO) and odorless mineral spirit(OMS) as experiment material,adopted Fourier transform infrared spectral reconstitution(SR-FTIR)technique to detect peroxide value(PV) in edible oils,basing on the PV determination is the rapid reaction of TPP with the hydroperoxides present in an oil to produce TPPO,which exhibits a readily measurable absorption band at 542 cm-1.The result showed that calibration standards,prepared by gravimetric addition of TPPO to a peroxide-free oil,were handled in the same manner,and a linear calibration equation relating the concentration of TPPO(expressed as the equivalent PV) to the absorbance of TPPO at 542 cm-1 relative to a baseline at 530 cm-1 in the reconstituted spectra was obtained,with a regression SD of ±0.067 mmol/kg oil.PV determinations on two sets of validation samples,spanning PV ranges of 0~1.5 and 1.5~10 mmol/kg oil,were carried out in parallel by the iodimetry and SR-FTIR-based FTIR procedures,and comparison of the results of duplicate analyses by the two methods indicated that the latter was more reproducible and slightly more sensitive.The SR-FTIR-based PV method,when implemented on an autosampler-equipped FTIR system,allowed for the automated analysis of 90 samples per hour.
分 类 号:TS227[轻工技术与工程—粮食、油脂及植物蛋白工程]
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