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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >A flow-based procedure exploiting the lab-in-syringe approach for the determination of ester content in biodiesel and diesel/biodiesel blends
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A flow-based procedure exploiting the lab-in-syringe approach for the determination of ester content in biodiesel and diesel/biodiesel blends

机译:利用基于流动的程序,利用实验室注射器方法,用于测定生物柴油和柴油/生物柴油混合物中的酯含量

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摘要

The ester content is an important parameter to be monitored in biodiesel for evaluation of the transesterification reaction yield and for assessing the purity of the final product. This is also a relevant quality parameter in diesel/ biodiesel blends to avoid frauds, because legislation establishes a minimum amount of biodiesel to be added to diesel. The official method EN14103 requires the addition of an alternative internal standard (methyl nonadecanoate) for analysis of biodiesel from bovine tallow because the methyl heptadecanoate is found in high amounts in this product. In this work, it is proposed a fast, simple, practical, and environmental friendly flow-based spectrophotometric procedure, which exploits the formation of the violet complex between Fe(III) and the hydroxamate generated by the reactions of the alkyl esters with hydroxylamine. All involved steps are carried out inside the syringe pump of a sequential injection analyzer (lab-in-syringe approach). A single phase is attained by using ethanol as mediator solvent between the organic sample and aqueous soluble reagents. Linear responses for biodiesel samples and diesel/biodiesel blends were obtained from 4-99%(v/v) to 2.0-40%(v/v) methyl esters, described by the equations: A = 0.342 + 0.00305C (r = 0.997) and A = 0.174 + 0.00503C (r = 0.999), respectively. The analytical curve can be obtained by in-line dilution of a methyl linoleate stock solution. For biodiesel samples, the coefficient of variation (n = 10), limit of detection (99.7% confidence level), and sampling rate were estimated at 0.8%, 0.36%(v/v), and 151 h(-1), respectively, whereas the corresponding values for the blend samples were 0.20%, 0.03%(v/v), and 12 h(-1), respectively. The procedure consumes only 860 mu g of hydroxylamine, 366 mu g of Fe-2(SO4)(3)center dot H2O, and 2.0 mL ethanol and generates ca. 3.0 mL of residue per determination. The results agreed with those obtained by official methods EN14103/2011 e EN14078, at the 95% confidence level.
机译:酯含量是在生物柴油中监测的重要参数,以评估酯交换反应产率并评估最终产品的纯度。这也是柴油/生物柴油混合物中的相关质量参数,以避免欺诈,因为立法建立了最低数量的生物柴油将添加到柴油中。官方方法EN14103需要添加替代的内标(甲基Nonadecanoate),用于分析来自牛牛肝的生物柴油,因为甲基庚二烷酸甲酯在本产品中以大量发现。在这项工作中,提出了一种快速,简单,实用,环保的流动系分光光度法,其利用Fe(III)与烷基酯与羟胺的反应产生的紫色复合物的形成。所有涉及的步骤都在顺序注射分析仪的注射泵(实验室注射器方法)内进行。通过在有机样品和水溶液水溶液之间使用乙醇作为介质溶剂来获得单相。通过等式描述的4-99%(v / v)至2.0-40%(v / v)甲酯,获得生物柴油样品和柴油/生物柴油共混物的线性响应:a = 0.342 + 0.00305℃(r = 0.997分别为a = 0.174 + 0.00503℃(r = 0.999)。通过在线稀释甲基Limolat储备溶液中可以获得分析曲线。对于生物柴油样品,变异系数(n = 10),检测限估计分别为0.8%,0.36%(v / v)和151h(-1)的估计值(99.7%)和取样率,而共混样品的相应值分别为0.20%,0.03%(v / v)和12h(-1)。该方法仅消耗860μg羟胺,366μgFe-2(SO 4)(3)中心点H 2 O,2.0ml乙醇并产生CA.每种测定3.0毫升残留物。结果同意通过官方方法EN14103 / 2011 E EN14078获得的结果,处于95%的置信水平。

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