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喷气燃料中抗氧剂2,6-二叔丁基对甲酚的高效液相分析 总被引:2,自引:0,他引:2
采用高效液相法分析喷气燃料HDF 1中的抗氧化剂 2 ,6 二叔丁基对甲酚 (简称BHT)含量 ,研究了二元混合流动相中甲醇 乙酸缓冲液的比例对燃料主体和BHT分离效果的影响 ,选择了最佳分离条件 (甲醇所占体积分数为 85 % ,流速为 1mL/min) ,在此条件下 ,可测出质量分数为 1× 10 -5的BHT。用该喷气燃料配制了BHT质量分数在 2 0× 10 -6到 12 0× 10 -6之间的标准溶液 ,考察了BHT质量分数与峰面积之间的关系 ,结果表明线性关系良好。 相似文献
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高效液相色谱法分离和测定2,6-二特丁基对甲酚和2-特丁基对甲酚 总被引:1,自引:0,他引:1
1引宫2,6H持了基对甲酚和}特丁基对甲酚为2种通用型酚类抗氧剂。它们对热、氧和老化有一定的防护作用。特别是2,*二特丁基对甲酚,其用途更为广泛,可作聚乙烯、聚氯乙烯及聚乙烯基酸等的稳定剂,作合成橡胶常用的防老剂,石油产品的抗氧添加剂,食品加工工业用的抗氧剂。2.特丁基对甲酚除作抗氧剂外,还是很好的阻燃剂。2,6H特了基对甲酸和2.特了基对甲酚都是在催化剂存在下,由对甲苯酚与异丁烯或异丁醇进行烷基化反应而得到的,由于反应条件的不同,而分别生成这两种不同的产物。如果反应条件控制得不好,很可能在生成其中一种主… 相似文献
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采用高效液相色谱法测定磷酸三甲苯酯中游离甲酚的含量.利用高效液相色谱外标法对试样进行分离、检测,获得最佳色谱条件.结果表明,最佳色谱条件:C18色谱柱(250 mm×4.6 mm×5μm),流动相为甲醇∶水(体积比为8∶2),流速1.0 mL/min,紫外检测器,检测波长280 nm,柱温35℃,等度洗脱,进样量10μL.方法的加标回收率为95.9%~98.9%,相对标准偏差为1.02%~2.55%,具有操作简便、快捷、准确度高的特点. 相似文献
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柱前衍生高效液相色谱法分离分析甲酚异构体 总被引:1,自引:0,他引:1
提出了柱前衍生高效液相色谱法同时分离测定邻甲酚、间甲酚和对甲酚的方法。含甲酚异构体的样品与衍生化试剂按1比8(质量比)混合,加热回流衍生2 h。3种异构体的转化率依次为98.1%,99.0%,98.5%。选用Eclipse XDB-C_(18)色谱柱作为反相色谱柱,以甲醇和水以体积比为35比65的混合溶液为流动相,在260nm波长处进行测定,乙酸邻甲酚酯、乙酸间甲酚酯的峰面积与其浓度在(0.05~3.75)×10~(-5)mol·L~(-1)范围内呈线性关系,而乙酸对甲酚酯在(0.03~2.25)×10~(-5)mol·L~(-1)之间呈线性关系,检出限(3S/N)依次为1.88×10~(-5),1.88×10~(-5),1.13×10~(-5)mol·L~(-1)。此方法应用于实际样品的测定,回收率分别为104%,95%,100%,相对标准偏差(n=7)分别为0.22%,2.34%,0.90%。 相似文献
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报道了一种检测油脂中的合成抗氧剂(BHT、BHA、TBHQ和PG)MLC方法,含有抗氧剂的油脂按1∶4(Voil:V2-propanol)被稀释、过滤,并且在没有前期萃取的情况下直接注射进样分析。研究了抗氧剂的MLC方法的检测条件。当C18色谱柱、胶束流动相中含0.08MSDS,5%(V/V)异丙醇和0.01mol/LNaH2PO4.H2O,胶束流动相的pH为3~4,检测波长为280nm,流速1ml/min时,在1~15μg/g的范围内标准曲线呈线性关系(r0.9992),4种抗氧剂的检测限为0.1~0.4μg/g。方法回收率为89.1%~99.9%。 相似文献
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反相高效液相色谱法同时测定苦豆子及其制剂中苦参碱和氧化苦参碱 总被引:1,自引:0,他引:1
建立了用反相高效液相色谱法测定苦豆子及其制剂中苦参碱和氧化苦参碱的方法。为苦豆子及其制剂的质量评价提供了一种方法。 相似文献
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反相高效液相色谱法测定七种中药中齐墩果酸 总被引:8,自引:0,他引:8
首次用反相高效液相色谱法分离并测定了地肤子、连翘、牛膝、泽兰、白花蛇舌草、夏枯草、柿蒂七种中药中的齐墩果酸。建立了中药中齐墩果酸分离、测定的色谱方法。色谱条件:ODS柱,甲醇+水(90+10)为流动相,紫外检测器检测波长207nm。本研究为扩大中药及植物中齐墩果酸药物资源的开发提供了简便、灵敏、准确的分离测定方法。 相似文献
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《Analytical letters》2012,45(14):2200-2209
A new, sensitive RP-HPLC method was developed for the determination of oseltamivir phosphate in capsules and plasma. The method was based on the reaction of the drug with 4-chloro-7-nitrobenzofurazan in borate buffer solution of pH 8.50. Isocratic chromatography was performed on a C18 column with acetonitrile–10 mM nitric acid (pH 3, 60 + 40, v/v) as the mobile phase with fluorescence detection (λex: 470 nm, λem: 541 nm). Mexiletine hydrochloride was used as an internal standard. Analytical parameters were evaluated. The calibration range was linear from 50.0–750.0 ng/ml. The mean percentage recovery in capsules and plasma were 99.95% and 95.42%, respectively. 相似文献
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Summary Ion interaction reagent RP-HPLC has been employed for the separation of some typical aliphatic and aromatic amines.
The effects on retention of the alkyl chain length of the eluent, and of the eluent flow-rate have been studied.
The use of solutions of hexylaminium-, octylaminium-and decylaminium-salicylate has been tested and compared, employing both
conductometric and spectrophotometric detection.
On the basis of the results obtained, the optimal experimental conditions can be chosen for each separation. Aliphatic and
aromatic mono and diamines can be separated and detected, with an average sensitivity of the order of 40 ng without any pretreatment
or derivatization.
The retention data obtained for amines, compared with those obtained with the same ion interaction reagents for anions, help
in the interpretation of the mechanism involved in the technique. 相似文献
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A validated reversed-phase high-performance liquid chromatographic (RP-HPLC) method was developed for the determination of bergenin in rat plasma. Bergenin in rat plasma was extracted with methanol, which also acted as a deproteinization agent. Chromatographic separation of bergenin was performed on a C(18) column, with a mobile phase of methanol-water (22:78, v/v) at a flow-rate of 0.8 mL/min and an operating temperature of 40 degrees C, and UV detection was set at 220 nm. The calibration curve was linear over the range 0.25-50 microg/mL (r = 0.9990) in rat plasma. The limit of quantification was 0.25 microg/mL using a plasma sample of 100 microL. The extraction recoveries were 83.40 +/- 6.02, 81.49 +/- 2.40 and 72.51 +/- 2.64% at concentrations of 0.5, 5 and 50 microg/mL, respectively. The intra-day and inter-day precision and accuracy were validated by relative standard deviation (RSD%) and relative error (RE%), which were in the ranges 3.74-9.91 and -1.6-8.0%. After intravenous administration to rats at the dose of 11.25 mg/kg, the plasma concentration-time curve of bergenin was best conformed to a two-compartment open model. The main pharmacokinetic parameters indicated that bergenin exhibited a wide distribution and moderate elimination velocity in rat. 相似文献
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兔肝金属硫蛋白亚型异构体的高效液相色谱分离与ESI-MS,MALDI-TOF-MS鉴定 总被引:2,自引:0,他引:2
由于金属硫蛋白(MT)基因的多态性,决定不同亚型的MT异构体的存在,MT亚型异构体的结构是MT功能研究的基础.通过离子交换柱可将MT分成MT-1和MT-2两个异构体,用不同条件的反相高效液相色谱(RP-HPLC)可将MT-1和MT-2分成不同的亚型异构体,并利用MALDI-TOFMS和LC-ESI-MS对比确定了它们的分子量.结果表明,兔肝MT在不同的pH条件下分离得到不同分子量的亚型异构体.在酸性条件下,MT-1可分为2个主要亚型异构体,分子量分别为6149.0和6244.5,而MT-2主要分为3个亚型异构体,分子量分别为6149.0,6244.0和6127.0.MT-1和MT-2有2个亚型异构体分子量相同的异构体存在.在酸性条件下,MT-1的2个异构体及MT-2分子量为6127的亚型异构体可稳定存在. 相似文献