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Direct Analysis of Synthetic Phenolic Antioxidants, and Fatty Acid Methyl Ester Stability in Biodiesel by Liquid Chromatography and High-Resolution Mass Spectrometry

机译:通过液相色谱和高分辨率质谱分析生物柴油中合成酚类抗氧化剂和脂肪酸甲酯稳定性的直接分析

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Methods to identify and quantify synthetic phenolic antioxidants, 3-tert-butyl-4-hydroxyanisole (BHA), butylated hydroxytoluene (BHT), tert-butyl-hydroquinone (TBHQ) and propyl gallate (PG), in biodiesel samples by using reversed-phase liquid chromatography (LC) were developed. Using a C18 phase with LC and UV detection showed co-elution between BHT and fatty acid methyl esters (FAME) in the biodiesel sample, whereas an alkyl phenyl modified stationary phase resulted in good separation of all antioxidants from the fatty acid matrix, and allowed more accurate quantification of antioxidants in biodiesel samples. The latter column was applied for further study. Calibration curves for the four antioxidants were constructed, and the limit of detection estimated. Good calibration linearity was observed over the investigated concentration range of 10-80ppm, with correlation coefficients (R-2) ranging from 0.9986 to 0.9995 for all antioxidants. LOD values of 0.010, 0.015, 0.0125 and 0.030ppm, and recoveries of 70 +/- 2, 85 +/- 2, 103 +/- 2 and 92 +/- 4% for PG, TBHQ, BHA and BHT at injected concentrations of 35ppm were established, respectively. The method was applied for quantification of antioxidants in biodiesel without addition of spiked antioxidants, then for biodiesel spiked with the four antioxidants, and a commercial source of biodiesel with BHT addition. Identification of FAME in the biodiesel samples was performed by using an instrument capable of ultra-high performance LC hyphenated with an electrospray Orbitrap mass spectrometer (UHPLC-ESI-OrbitrapMS). The stability of antioxidants and FAME in different samples was then investigated. Total FAME C18 content decreased to 52 +/- 4% w/w after 1week, and 29 +/- 6% w/w after 8weeks in the test sample without antioxidants; FAME content and antioxidant composition were stable in the samples with antioxidants added, even after 8weeks exposure to sunlight.
机译:通过使用反转,鉴定和定量合成酚醛抗氧化剂,3-叔丁基-4-羟基烷(BHA),丁基羟基苯基(BHT),叔丁基 - 氢醌(TBHQ),叔丁基 - 氢醌(TBHQ),叔丁基 - - 氢醌(TBHQ),叔丁基 - - 氢醌(PG),产生相液相色谱(LC)。使用具有LC和UV检测的C18相和紫外检测在生物柴油样品中的BHT和脂肪酸甲酯(FAME)之间的共洗,而烷基苯基改性固定相使所有来自脂肪酸基质的抗氧化剂良好分离,并允许更准确地定量生物柴油样本中的抗氧化剂。后一栏被应用于进一步研究。构建了四种抗氧化剂的校准曲线,并估计了检测极限。在调查的浓度范围内观察到良好的校准线性,在10-80ppm的浓度范围内,相关系数(R-2)为所有抗氧化剂的0.9986至0.9995。 LOD值0.010,0.015,0.0125和0.030ppm,并回收70 +/- 2,85 +/- 2,103 +/- 2和92 +/- 4%,用于注射浓度下的PG,TBHQ,BHA和BHT分别建立了35ppm。该方法用于定量生物柴油中的抗氧化剂,而不加入尖刺抗氧化剂,然后用于与四种抗氧化剂掺入的生物柴油,以及BHT加入的生物柴油商业来源。通过使用能够用电喷雾横向质谱仪(UHPLC-ESI-ORBITRAPMS)连字符的超高性能LC的仪器进行生物柴油样本中的识别生物柴油样本中的识别。然后研究了不同样品中抗氧化剂和名称的稳定性。总名称C18含量在1周后的52 +/- 4%w / w,在试样8周后29 +/- 6%w / w,无抗氧化剂在没有抗氧化剂的情况下;由于8周暴露在阳光下,添加抗氧化剂的样品中,在样品中稳定,在样品中稳定。

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