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双语推荐:羟基苯甲酸酯类防腐剂

羟基苯甲酸酯类防腐剂即为一种常用的防腐剂防腐剂的使用必须按照国家相关的卫生安全标准,不许超剂量、超范围使用。但是,实际生活中,经才会出现对羟基苯甲酸酯类防腐剂的具体添加含量超标的情况。因此,做好对食品防腐剂含量的测定至关重要。
isacommonpreservativeparabens.Thepreservativesusedmustbeinaccordancewiththenationalstandardsofhygieneandsafetyrelated,not superdose,thescopeoftheuseofultra.However,inreallife,thespecificcontentexceedthestandardwil beaddedtotheparabenspreservatives.Therefore, goodonthedeterminationofpreservativesinfood.

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目的建立高效液相色谱同时测定糖果、蜜饯和饮料中19种常用食品添加剂的分析方法。方法样品经亚铁氰化钾和乙酸锌溶液沉淀蛋白后,采用Poroshell 120 EC-C18(4.6 mm×100 mm,2.7μm)色谱柱分离,甲醇和0.02 mol/L乙酸铵水溶液为流动相进行梯度洗脱,二极管阵列检测器多波长(230、254、274、480和630 nm)检测,外标法定量。结果 19种食品防腐剂、甜味剂和色素组分得以有效分离。色素和咖啡因线性范围为0.5~12.5 mg/L,对羟基苯甲酸酯类线性范围为1~25 mg/L,其他添加剂线性范围为2~50 mg/L,相关系数均大于0.999。方法检出限为1.0 mg/L,测定低限为10.0 mg/kg。加标回收率为81.4%~110.9%,相对标准偏差值为0.34%~4.6%(n=6)。结论 此方法具有快速、准确且样品处理简单等优点,适用于糖果、蜜饯和饮料中多种添加剂的快速测定。
Objective Todevelop a simple and rapid method for the simultaneous determination of 19 food additives in candies, preserves and beverages by high performance liquid chromatography (HPLC). Methods The sample was extracted by water and precipitated of protein with K4[Fe(CN)6] and Zn(Ac)2 solu-tion. The separation was achieved on a poroshell 120 EC-C18 column (4.6mm ×100 mm, 2.7μm) by using me-thanol and 0.02 mol/L NH4Ac as mobile phase with the gradient eluent. Components were detected with a diode array detector (DAD) at 230, 254, 274, 480 and 630 nm, respectively. The quantification was performed by the external standard method.ResultsNineteen food additives, including preservatives, sweeteners and pigments, were efficiently separated. The method showed a good linearity for 19 food additives with correlation coeffi-cients (r) above 0.999 over the range of 0.5~12.5 mg/L for pigments and caffeine, 1~25 mg/L for p-hydroxybenzoic acid esters, 2~50 mg/L for the others compounds.

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