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无汞盐吸收-超声波浸提检测干果SO2残留方法的探讨 被引量:3
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作者 李文生 郭振忠 +5 位作者 冯晓元 王宝刚 闫国华 杨军军 张长松 王纪华 《食品工业科技》 CAS CSCD 北大核心 2008年第10期261-263,共3页
对盐酸副玫瑰苯胺法测定食品中SO2进行改进,以甲醛代替剧毒试剂四氯化汞,建立了超声波浸提、无汞盐吸收液检测干果SO2残留的方法。该方法操作简便、安全,SO2含量与吸光值线性关系良好,相关性为R2=0.9995,检出限为0.8mg/kg,加标回收率为9... 对盐酸副玫瑰苯胺法测定食品中SO2进行改进,以甲醛代替剧毒试剂四氯化汞,建立了超声波浸提、无汞盐吸收液检测干果SO2残留的方法。该方法操作简便、安全,SO2含量与吸光值线性关系良好,相关性为R2=0.9995,检出限为0.8mg/kg,加标回收率为92.81%~107.76%。 展开更多
关键词 无汞盐吸收液 超声波加速提取 SO2残留 干果
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四氯汞钠吸收-超声快速提取法测定食品中的亚硫酸盐 被引量:7
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作者 马占玲 曾凌 +1 位作者 励建荣 章超桦 《科学技术与工程》 北大核心 2013年第3期786-789,共4页
探究盐酸副玫瑰苯胺做显色剂时样品的最佳处理方法。每种样品采用六种方法处理后进行测量。结果表明用四氯汞钠做吸收剂测得的结果高于甲醛和水。且室温下,样品中加入四氯汞钠后,微波提取1.5 h与用四氯汞钠直接浸泡4 h测得的结果相当。... 探究盐酸副玫瑰苯胺做显色剂时样品的最佳处理方法。每种样品采用六种方法处理后进行测量。结果表明用四氯汞钠做吸收剂测得的结果高于甲醛和水。且室温下,样品中加入四氯汞钠后,微波提取1.5 h与用四氯汞钠直接浸泡4 h测得的结果相当。该方法线性方程为y=0.031 2x+0.001 6,相关系数为R2=0.999 7。测定样品的相对标准偏差在2.5%~3.2%之间,回收率在92%~102%之间。该方法操作简便,重现性好,省时,可用于食品中亚硫酸盐的测定。 展开更多
关键词 盐酸副玫瑰苯胺法 四氯汞钠 超声波加速提取 亚硫酸盐 食品
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Evaluating the performances of accelerated-solvent extraction, microwave-assisted extraction, and ultrasonic-assisted extraction for determining PCBs, HCHs and DDTs in sediments 被引量:1
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作者 张蓬 葛林科 +1 位作者 周传光 姚子伟 《Chinese Journal of Oceanology and Limnology》 SCIE CAS CSCD 2011年第5期1103-1112,共10页
Three extraction techniques have been recently used for the quantitative extraction of semi-volatile organic pollutants in sediments, i.e. accelerated solvent extraction (ASE), microwave assisted extraction (MAE) ... Three extraction techniques have been recently used for the quantitative extraction of semi-volatile organic pollutants in sediments, i.e. accelerated solvent extraction (ASE), microwave assisted extraction (MAE) and ultrasonic assisted extraction (UAE). However, their extraction efficiencies have rarely been quantitatively compared using rigorous mathematical methods. In this paper, one-way analysis of variance (ANOVA) was employed to evaluate the performance of ASE, MAE and UAE in the overall extraction of PCBs, DDTs and HCHs by analysis of their recoveries from the Standard Reference Material IAEA-417, a sediment sample certified by many international laboratories. Conclusions were drawn at a significance level of P〈 0.05. No significant differences were found among the mean values for method recoveries using ASE, MAE and UAE. The mean values for real recoveries using ASE and MAE were nearly identical, but the real recovery using UAE was much lower. The concentrations of all PCBs, DDTs and HCHs except for CB52 and o,p'-DDT using UAE were the lowest. Comparing the results obtained using ASE with MAE, the concentrations of CB28, CB52, CB138, ct-HCH, [3-HCH, p,p'-DDE and p,p'-DDD were nearly identical, while the concentrations of other compounds were significantly different. Based on the low recoveries, it was concluded that UAE is a relatively inefficient extraction method, while ASE and MAE are equivalent methods. Taking into consideration the relative standard deviation (RSD) values, solvent volume, extraction time, and purchasing costs of the apparatus, MAE was considered superior to ASE for extraction of PCBs, DDTs and HCHs. 展开更多
关键词 extraction technique sediment PCB HCH DDT
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