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固相微萃取技术在农药残留分析中的应用 总被引:1,自引:0,他引:1
固相微萃取技术是一种崭新的无溶剂萃取分离技术。文中对影响萃取效果的因素进行了综述,并对固相微萃取技术在农药残留分析中的应用作出概述,引用文献56篇。 相似文献
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固相微萃取法在禁用偶氮染料检测中的应用初探 总被引:5,自引:1,他引:4
将固相微萃取技术应用于出口染色纺织品及皮革制品中禁用偶氮染料检验,偶染料经连二亚硫酸钠还原成芳胺后,用固相微萃取技术萃取富集后,用GC-MS分析。实验了萃取方式、萃取纤维、pH值、浓度、温度、萃取时间及色谱条件等因素对萃取与测定的影响。 相似文献
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采用溶胶-凝胶方法合成了石墨烯复合材料,将其均匀地涂在铜丝表面制备了石墨烯固相微萃取纤维,结合固相微萃取-气相色谱-电子捕获检测器(SPME-GC-ECD)技术,建立了对环境中类二英多氯联苯(DL-PCBs)的直接测定方法。实验优化了萃取温度、萃取时间、pH值和离子强度等固相微萃取条件。在优化条件下,石墨烯固相微萃取纤维较商品化纤维(100μm PDMS、75μm CAR/PDMS、85μm PA)的萃取效率平均高2倍。对于DL-PCBs分析,该方法在0.05~3.5μg.L-1范围内呈良好线性(除PCB169外,r2均高于0.99),检出限为4.7~8.8 ng.L-1,单个纤维间及纤维与纤维间的相对标准偏差分别为1.4%~8.1%和2.4%~12.8%。该纤维对12种环境样品中DL-PCBs加标0.5μg.L-1和2 ng.g-1的回收率为87%~120%。方法简单、快速、灵敏,可实现对多氯联苯的痕量检测。 相似文献
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固相微萃取技术在形态分析中的应用进展 总被引:3,自引:0,他引:3
形态分析比传统的元素分析能提供更为丰富的信息,成为当今分析化学领域前沿课题之一,而固相微萃取(SPME)是近十年来发展起来的新型分离富集技术,简便快速、无污染、易于和其它技术联用.近几年来才开始将固相微萃取应用到形态分析,二者结合对形态分析的发展具有促进作用,本文就固相微萃取技术在元素有机化合物形态分析中的应用进行了评述. 相似文献
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电化学分析法是应用电化学原理和技术,利用化学电池内被分析溶液的组成及含量与其电化学性质的关系而建立起来的一类分析方法,常用仪器为具有多功能的电化学工作站. 详细介绍了宽频介电谱仪的电化学工作站功能,包括其仪器结构组成、仪器原理、先进的功能应用及仪器本身独特优势. 相似文献
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碳纤维上电沉积Pd-Ag合金纳米粒子链及其氢传感性能 总被引:1,自引:0,他引:1
在碳纤维上采用三脉冲电沉积的方法制备出钯银合金纳米粒子链.把表面覆盖有Pd-Ag合金纳米粒子链的碳纤维组装成氢气传感器.采用扫描电子显微镜(SEM)和X射线能谱(EDX)表征了合金纳米粒子链的形貌和成分,应用CHI660B电化学工作站测试其氢传感性能.结果表明,在钯、银离子摩尔比为15∶1的电解液中,在-1.0--1.5 V下,成核5-40 ms;在-0.25--0.35 V,生长200-300 s的条件下,即可获得银的质量分数为16.0%-25.0%的钯银合金纳米粒子链阵列.在室温下,传感器对在0.30%-5.00%(φ,体积分数,下同)范围内的氢气有响应,最快响应时间约为300 s,灵敏度最高可达31.0%;氢在0.30%-1.20%的范围内响应电流与氢气浓度成线性关系,超过4.00%时响应电流不再随浓度的增加而变化;在低于3.50%的浓度下氢传感器的重现性良好. 相似文献
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采用浸渍技术在多孔的氧化钇稳定的氧化锆(YSZ)中制备了纳米CuO敏感材料,并以其为敏感电极,YSZ为固体电解质,制备了一种新型的电流型NO2传感器。采用X射线衍射仪和扫描电子显微镜表征了NO2传感器的相组成和微观形貌,应用IM6e型电化学工作站测试了其气敏性能。结果表明,CuO颗粒粒径约为100 nm,且与基体结合紧密。在500~600℃时,传感器对NO2表现出良好的敏感性。在极化电压为-300 mV,NO2体积分数为0~5.0×10-4时,传感器的响应电流值与NO2浓度之间呈良好的线性关系。在被测气体总流量为400 cm3/min时,传感器信号90%的响应和恢复时间均为50 s。传感器响应信号在测试时间内具有良好的稳定性。共存气体O2和CO2对传感器的敏感性几乎没有影响。 相似文献
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O. Egorov J. W. Grate J. Ruzicka 《Journal of Radioanalytical and Nuclear Chemistry》1998,234(1-2):231-235
A rapid automated flow injection analysis (FIA) procedure was developed for efficient separation of Am and Pu from each other
and from interfering matrix and radionuclide components using a TRU-resin™column. Selective Pu elution is enabled via on-column reduction. The separation was developed using on-line radioactivity
detection. After the separation had been developed, fraction collection was used to obtain the separated fractions. In this
manner, a FIA instrument functions as an automated separation workstation capable of unattended operation. 相似文献
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根据微量硫分析仪测定人工煤气中微量硫化物的原理和仪器本身的特点,分析了用该法测定甲醇合成气中微量硫化物时,温度、气体配比等因素对测定结果的影响,指出了测定时应注意的事项。 相似文献
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《Journal of Energy Chemistry》2017,26(6):1050-1066
The recent development of Cu-based electrocatalysts for electrochemical reduction of carbon dioxide(CO_2) has attracted much attention due to their unique activity and selectivity compared to other metal catalysts. Particularly, Cu is the unique electrocatalyst for CO_2 electrochemical reduction with high selectivity to generate a variety of hydrocarbons. In this review, we mainly summarize the recent advances on the rational design of Cu nanostructures, the composition regulation of Cu-based alloys, and the exploitation of advanced supports for improving the catalytic activity and selectivity toward electrochemical reduction of CO_2. The special focus is to demonstrate how to enhance the activity and selectivity of Cubased electrocatalyst for CO_2 reduction. The perspectives and challenges for the development of Cu-based electrocatalysts are also addressed. We hope this review can provide timely and valuable insights into the design of advanced electrocatalytic materials for CO_2 electrochemical reduction. 相似文献
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在电化学工作站上以铜箔为工作电极,以硝酸银和PVP混合液作为前驱溶液,利用循环伏安法电辅助制备了纳米银,得到在铜箔上紧密均匀分布的纳米银颗粒聚集体作为SERS基底。通过X射线粉末衍射、X射线光电子能谱、扫描电子显微镜等表征手段,对铜箔上负载的银纳米颗粒进行了形貌和成分的表征,探讨了PVP及电辅助方法对纳米银形貌及基底SERS活性的影响。以4-巯基吡啶和罗丹明6G为探针溶液研究了制备基底的SERS活性,同时还对基底的均匀性进行了研究,结果表明所制备的SERS基底具有良好的性能。 相似文献
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A wide-range bipolar electrochemical integrator/potentiostat is described. The instrument uses digital logic for timing and switching of analog control and output functions. Digital output is included with variable proportioning for adjustment to concentration units. Currents ranging from a few nA to 10 mA may be monitored and integrated with high precision. The capabilities of the instrument are illustrated by integral monitoring of an enzyme reaction, integration of an organic electrolysis at a solid electrode for a fixed time, and integration of a dropping mercury electrode current over several drop lives. 相似文献
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Electrospinning with a simple and controllable process has extremely received considerable concerns by virtue of the fabrication and development of nanofibers. Moreover, nanofibers are playing an increasing impact on energy conversion and storage devices, especially for fuel cells based on oxygen reduction reaction(ORR), in view of the rich porosity, large surface area, excellent mass transportation and simply tunable composition, as well as good mechanical strength. In this review, we mainly introduce the primary principle of electrospinning technique, electrochemical reaction mechanism of ORR and synthetic strategies, and summarize the recent advances of unique non-noble-metal nanofibers on the basis of metal-organic framework(MOF) derivatives, single-atom catalysts(SACs) and transition metal oxides. More importantly, we emphasize on the influences of the components, morphology and architecture of advanced electrospun catalysts on their correspon-ding electrochemical performances towards ORR. Finally, the remaining puzzles and perspectives for further development of the electrospinning nanofibers involving electrocatalysis are presented. It is envisioned that this review would offer an important direction in designing novel electrocatalysts based on electrospinning nanofibrous structures and developing their potential. 相似文献