共查询到19条相似文献,搜索用时 171 毫秒
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植物样品中单宁的微波溶出快速测定法研究 总被引:16,自引:0,他引:16
研究了利用微波代替一般的沸水浴处理试样的方法。对不同植物样品中单宁的浸提测定,与常规方法做了对照,并讨论了微波功率、时间、酸度等因素对测定结果的影响。研究表明,此法可大大地缩短测定时间,提高测定效率,节省人力、物力,不污染环境,便于大批量样品的测定,相对标准偏差≤1.4%,测定结果较为满意。为植物样品中单宁的测定,提供了一个快速、简便、准确的分析方法,并可借鉴于其它样品的测定。 相似文献
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分子印迹固相萃取及其应用 总被引:22,自引:19,他引:22
系统地介绍了分子印迹固相萃取的原理、特点、发展现状及其发展趋势,并重点对分子印迹固相萃取技术在环境和生物样品前处理中的应用作了较详细的综述。共引用文献100篇。 相似文献
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生物,环境样品和食品中铅的痕量分析 总被引:2,自引:0,他引:2
主要根据近七年来发表的有关论文,综述了我国生物、环境样品和食品中铅和痕量分析技术进展,内容包括分子光谱、原子光谱、电化学和其他分析方法,以及联用技术和前处理等方面,收集文献393篇。 相似文献
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环境及生物样品中铂分析研究的进展 总被引:12,自引:0,他引:12
介绍了近年来环境及生物样品中铂分析研究的进展。特别是对大气尘埃及土壤中铂的分布,转移规律以及植物和动物样品中不同化学形态铂的分离,分析方法及分析结果作了着重介绍。 相似文献
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扫描电子显微镜对样品的要求及样品的制备 总被引:7,自引:0,他引:7
李剑平 《分析测试技术与仪器》2007,13(1):74-77
扫描电子显微镜对样品的要求很严,要求样品必须是固体,且做到五无:无毒、无放射性、无污染、无磁、无水分,成分稳定,块状样品大小要适中,粉末样品要进行特殊处理,对不导电和导电性能差的样品要进行镀膜,且要选择适当的镀膜仪,方能达到理想的分析效果. 相似文献
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近二十年来,高分辨率27Al核磁共振(27Al NMR)广泛应用于研究Al(Ⅲ)离子水解过程,Al(Ⅲ)与环境生物配体的配位化学,环境与生物样品中铝含量测定和形态分析,监测铝在植物、动物、酵母菌等微生物中的转运过程,具有快速、直接、非破坏性等优点。27Al NMR不仅适用于高浓度的溶液,也可应用于低浓度(10-6mol·L-1)的实际环境、生物样品。应用27Al MASNMR可直接对固态样品中铝的存在状态和含量进行表征和测量。本文中对27Al NMR的应用进展作一评述,并总结了近二十年来文献发表的27Al化学位移数据。引用文献70余篇。 相似文献
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环境样品中硝基苯类化合物的分析方法研究进展 总被引:4,自引:0,他引:4
主要介绍了我国近年来在环境样品中硝基苯类化合物的分析研究进展,内容包括:光度法(还原-偶氮光度法、阻抑动力学光度法、化学计量学分光光度法、人工神经网络-分光光度法)、气相色谱法(固相微萃取-毛细管气相色谱法、树脂吸附-气相色谱法、液-液微萃取气相色谱法、超声萃取-气相色谱法)、高效液相色谱法(反相高效液相色谱法、固相萃取-高效液相色谱法)和极谱法等分析方法。 相似文献
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Tianliang Hu Run Chen Qiang Wang Chiyang He Shaorong Liu 《Journal of separation science》2021,44(1):274-309
Sample pretreatment is essential for the analysis of complicated real samples due to their complex matrices and low analyte concentrations. Among all sample pretreatment methods, solid‐phase extraction is arguably the most frequently used one. However, the majority of available solid‐phase extraction adsorbents suffer from limited selectivity. Molecularly imprinted polymers are a type of tailor‐made artificial antibodies and receptors with specific recognition sites for target molecules. Using molecularly imprinted polymers instead of conventional adsorbents can greatly improve the selectivity of solid‐phase extraction, and therefore molecularly imprinted polymer‐based solid‐phase extraction has been widely applied to separation, clean up and/or preconcentration of target analytes in various kinds of real samples. In this article, after a brief introduction, the recent developments and applications of molecularly imprinted polymer‐based solid‐phase extraction for determination of different analytes in complicated real samples during the 2015‐2020 are reviewed systematically, including the solid‐phase extraction modes, molecularly imprinted adsorbent types and their preparations, and the practical applications of solid‐phase extraction to various real samples (environmental, food, biological, and pharmaceutical samples). Finally, the challenges and opportunities of using molecularly imprinted polymer‐based solid‐phase extraction for real sample analysis are discussed. 相似文献
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M. Barriada-Pereira M.J. González-Castro P. López-Mahía D. Prada-Rodríguez E. Fernández-Fernández 《Talanta》2007,71(3):1345-1351
A method to determine organochlorine pesticides in horticultural samples (lettuce, tomato, spinach, potato, turnip leaf and green bean) using pressurized liquid extraction (PLE) is described and compared with microwave assisted extraction (MAE). Significant parameters affecting PLE procedure such as temperature, static extraction time and extraction solvent were optimised and discussed. Clean-up of extracts was performed by solid phase extraction (SPE) using a carbon cartridge as adsorbent. Pesticides were determined by gas chromatography and electron capture detection (GC-ECD). Analytical recoveries obtained were ca. 100% and the relative standard deviations were lower than 15% for most of the studied pesticides with the proposed methods in each analysed matrix. 相似文献
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《Journal of separation science》2018,41(13):2750-2758
An analytical method is presented for the determination of paraben preservatives in semisolid cream samples by matrix solid‐phase dispersion combined with supramolecular solvent‐based microextraction. Due to the oily and sticky nature of the sample matrix, parabens were first extracted from the samples by matrix solid‐phase dispersion using silica as sorbent material with a clean‐up performed with tetrahydrofuran in the elution step. The eluate (500 μL), 1‐decanol (120 μL), and water (4.4 mL) were then mixed in a polyethylene pipette to form supramolecular solvent. Finally, the analytes in the supramolecular solvent were separated and determined by liquid chromatography with ultraviolet detection. Under optimal extraction conditions, the extraction recoveries of the studied compounds were obtained in the range of 63–83%. The limits of detection for the analytes were between 0.03 and 0.04 μg/g. The precision of the method varied between 4.0–6.7 (intraday) and 6.2–7.9% (interday). Finally, the optimized procedure was applied to the determination of the target preservatives in a variety of cream samples (diaper rash, skin allergy, face and hand moisturizing) with satisfactory recoveries (86–102%). 相似文献
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Ümit DivrikliLatif Elçi 《Analytica chimica acta》2002,452(2):231-235
A cerium(IV) hydroxide coprecipitation method was developed for the determination of some trace elements (Cu, Co, Pb, Cd, Ni) in aqueous solutions, water and sediment samples by flame atomic absorption spectrometry (AAS). Several parameters governing the efficiency of the coprecipitation method were evaluated including pH of sample solution, amount of carrier element, volume of sample solution and the effect of possible matrix ions The procedure was validated by the analysis of GBW 07309 standard reference material sediment and by use of a method based on a solid phase extraction. 相似文献
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Li‐Fei Huang Bo Jia Lin Jiang Wei‐Lun Liu Li‐Ya Xia Yun‐Kai Lv 《Journal of separation science》2019,42(4):843-850
A restricted‐access material–hybrid monolithic column was prepared based on single‐component organosiloxane and dynamic grafting of δ‐gluconolactone for on‐line solid phase extraction of tetracycline antibiotic residues from milk. The hybrid monolithic column was prepared in a stainless‐steel chromatographic column using methyltrimethoxysilane as the single precursor. δ‐Gluconolactone was covalently coupled to aminopropyl derivatized hybrid monolithic column, which formed hydrophilic structures on the surface of the pore of the restricted‐access material–hybrid monolithic column. The columns were characterized by scanning electron microscopy, thermogravimetric analysis, Fourier transform infrared spectroscopy, nitrogen adsorption, contact angle analysis, dynamic adsorption, and chromatographic performance evaluation. The restricted‐access material–hybrid monolithic column was applied to the on‐line extraction of tetracycline residues from milk. An enrichment factor of 15.8 and a good sample clean‐up effect were obtained under the optimized conditions. The recoveries of the three spiked milk samples were between 81.7 and 102.5% with relative standard deviations (n = 3) in the range of 2–5%. The limits of detection (S/N = 3) for target compounds were in the range of 3.80–9.03 μg/kg. The results show that the on‐line extraction using the restricted‐access material–hybrid monolithic column was powerful for food sample pretreatment with high selectivity and good clean‐up effect. 相似文献
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Even after emergence of most advanced instrumental techniques for the final separation, detection, identification and determination of analytes, sample handling continues to play a basic role in environmental analysis of complex matrices. In fact, sample preparation steps are often the bottleneck for combined time and efficiency in many overall analytical procedures. Thus, it is not surprising that, in the last two decades, a lot of effort has been devoted to the development of faster, safer, and more environment friendly techniques for sample extraction and extract clean up, prior to actual instrumental analysis. This article focuses on the state of the art in sample preparation of environmental solid biological samples dedicated to persistent organic pollutants (POPs) analysis. Extraction techniques such as Soxhlet extraction, sonication-assisted extraction, supercritical fluid extraction (SFE), microwave-assisted extraction (MAE), pressurised liquid extraction (PLE) and matrix solid-phase dispersion (MSPD) are reviewed and their most recent applications to the determination of POPs in biota samples are provided. Additionally, classical as well as promising novel extraction/clean-up techniques such as solid phase microextraction (SPME) are also summarized. Finally, emerging trends in sample preparation able to integrate analytes extraction and their adequate clean-up are presented. 相似文献