Results 11 to 20 of about 652,215 (151)

Determination of Maleic Acid and Fumaric Acid in Starch and Starch Products Using SPE-UHPLC Method(SPE-UHPLC测定淀粉及淀粉制品中丁烯二酸类酸度调节剂) [PDF]

open access: yesShipin kexue jishu xuebao, 2015
In the present study, a solid-phase extraction ultra high performance liquid chromatographic(UHPLC)method was established for the analysis of maleic acid, fumaric acid, and maleic anhydride in starch and starch products. Starch samples were cleaned up by
BIE Wei(别 玮)   +3 more
doaj   +1 more source

Molecularly Imprinted Solid-phase Extraction Coupled to Capillary Electrophoresis for Determination of Trichlorfon in Grape Wine(分子印迹固相萃取-毛细管电泳检测葡萄酒中“敌百虫”) [PDF]

open access: yesShipin kexue jishu xuebao, 2013
In this study, using the prepared trichlorfon molecularly imprinted polymer as sorbent, a novel method for the determination of trichlorfon residues in grape wine was developed by utilizing molecularly imprinted solid-phase extraction coupled to ...
ZHAO Tao(赵 涛)   +4 more
doaj   +1 more source

磁性离子液体石墨烯-固相萃取水中三嗪类除草剂

open access: yesGongye shui chuli, 2020
采用微乳共沉淀法制备磁性离子液体石墨烯(MILG),将其作为磁性固相萃取吸附剂,结合超高效液相色谱-串联质谱法实现对环境水样中7种三嗪类除草剂的定量分析。通过对影响因素的优化,在中性溶液中采用10 mgMILG作为萃取剂,吸附20 min萃取效果最佳。7种三嗪类除草剂的检出限为1.1~2.8 ng/L,实际水样中加标回收率为57.8%~101.2%,相对标准偏差在9.1%以内。
鲍秀敏   +6 more
doaj  

Applications of carbon nanotubes in the solid phase extraction(碳纳米管在固相萃取中的应用)

open access: yesZhejiang Daxue xuebao. Lixue ban, 2015
固相萃取技术(SPE)作为一种分析物提取和样品前处理方法,相比于传统的液液萃取更利于目标分析物的分离,提高痕量分析物的检出能力和被测物的回收率,同时减少对环境的二次污染,且操作过程简单方便,耗时较短.碳纳米管(CNTs)的独特性能使其成为非常有吸引力的SPE吸附材料.介绍了碳纳米管在农残、药品、有机化合物、无机金属离子等检测中的应用,并对碳纳米管在分析领域中的应用前景进行了展望.
CHENBing(陈冰)   +4 more
doaj   +1 more source

大肠杆菌细胞膜固定相萃取辣木籽抗菌肽Extraction of Moringa oleifera seed antimicrobial peptides by E.coli cell membrane stationary phase

open access: yesZhongguo youzhi, 2022
制备大肠杆菌细胞膜固定相(E.coli cell membrane stationary phase,ECMSP),研究其对辣木籽抗菌肽的萃取效果。研究超声时间、超声功率对大肠杆菌破壁效果的影响,分析大肠杆菌细胞膜与大孔硅胶的吸附特征及ECMSP对辣木籽抗菌肽的吸附效果,明确萃取前后抑菌活力变化及反相-高效液相色谱(RP-HPLC)差异峰。结果表明:在超声功率500 W、超声时间30 min条件下,大肠杆菌破壁效果较好;大孔硅胶对大肠杆菌细胞膜的饱和吸附值(Csmax)为9.98 μg/mg、吸附常数 ...
和丽1,许映月1,陈凤敏1,黄艾祥1,王雪峰1,2 HE Li1, XU Yingyue1, CHEN Fengmin1, HUANG Aixiang1, WANG Xuefeng1,2
doaj   +1 more source

Research on methods for determination of diazepam residue in animal original food(动物源性食品中地西泮残留量的检测方法研究)

open access: yesZhejiang Daxue xuebao. Lixue ban, 2019
采用高效液相色谱法(HPLC)、气相色谱质谱联用法(GC-MS/MS)以及液相色谱质谱联用法(HPLCMS/ MS)测定动物源性食品中镇静剂类药物地西泮的残留量。将样品均质粉碎后,经乙腈提取,固相萃取小柱净化后上机检测,外标法定量。实验证明,当固相萃取的洗脱液中甲醇与乙酸溶液的体积比为70:30 时,洗脱效率最高。在不同仪器条件下,地西泮在各自浓度范围内的线性关系良好,相关系数(r2) 均大于0.999,回收率在 84.6%~ 101.7%,相对标准偏差(RSD) 在0.52%~9.44% (n=3 ...
DINGYuqi(丁宇琦)   +3 more
doaj   +1 more source

Determination of tiamulin and valnemulin drug residues in aquatic products by ion exchange olid phase extraction-ultra performance liquid chromatography-tandem mass spectrometry(离子交换固相萃取-超高效液相色谱-串联质谱法同时测定水产品中泰妙菌素和沃尼妙林残留量)

open access: yesZhejiang Daxue xuebao. Lixue ban, 2019
建立了一种强阳离子固相萃取结合超高效液相色谱-串联质谱法同时测定水产品中泰妙菌素和沃尼妙林残留量的分析方法。样品经乙腈提取和Oasis MCX 固相萃取柱净化后,以乙腈-0.05 %甲酸5 mmoL·L-1 乙酸铵水溶液为流动相,经Waters ACQUITY UPLC BEH C18 色谱柱梯度洗脱分离,在电喷雾正离子多反应监测模式下,用内标法分析泰妙菌素,用外标法分析沃尼妙林。结果显示,泰妙菌素和沃尼妙林在0.1~10.0 ng·mL-1 内具有良好的线性关系,相关系数r 均大于0.999 9 ...
ZONGJingjing(宗婧婧)   +4 more
doaj   +1 more source

Analysis of Flavor Characteristics of Cold Brew and Hot Brew Coffee by GC-MS and Consumer Test with Emoticons(GC-MS结合基于表情符号的消费者测评分析冷萃与热萃咖啡风味特征) [PDF]

open access: yesShipin kexue jishu xuebao
In order to study the aroma differences of coffee liquid at different extraction temperatures and the correlation between sensory evaluation and aroma compounds, this study used three types of commercial cold brew coffee and three types of commercial hot
YANG Aolin(杨傲林)   +9 more
doaj   +1 more source

全自动固相萃取净化-高效液相色谱法测定 食用植物油中苯并(a)芘含量Determination of benzo(a)pyrene in edible vegetable oil by automated solid phase extraction-high performance liquid chromatography

open access: yesZhongguo youzhi, 2023
为提高工作效率,降低误差,建立分子印迹柱全自动固相萃取净化-高效液相色谱法测定食用植物油中苯并(a)芘含量的方法。样品经正己烷提取,采用全自动固相萃取仪进行分子印迹柱净化,C18色谱柱分离,高效液相色谱-荧光检测器检测。结果表明:苯并(a)芘在0.5~20.0 ng/mL质量浓度范围内与峰面积线性关系良好,相关系数为 0.999 9,方法检出限为0.09 μg/kg,定量限为0.30 μg/kg,加标回收率为91.7%~111.8%,相对标准偏差为2.0%~8.2%,与国标方法的检测结果不存在显著性差异;
曾云军,汪泽生 ZENG Yunjun, WANG Zesheng
doaj   +1 more source

马铃薯过氧化物酶催化氧化快速降解双酚A

open access: yesGongye shui chuli, 2021
通过构建双水相萃取体系,从马铃薯淀粉加工废水中萃取过氧化物酶,再经透析、冻干得马铃薯过氧化物酶固体酶粉,用于催化H2O2快速降解双酚A(BPA)。结果表明,在室温,pH为6,200 U/mL马铃薯过氧化物酶催化1.0 mmol/L H2O2氧化初始浓度为0.8 mmol/L BPA的条件下,反应10 min后,BPA的降解率可达99%以上,对于修复水体具有极大的潜在应用价值。
王鑫鑫   +8 more
doaj  

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