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毛细管气相色谱法测定水和废水中的丙烯酰胺 总被引:2,自引:0,他引:2
本文采用毛细管色谱法建立了水和废水中丙烯酰胺的测定程序。在此,以活性炭柱吸附,浓缩样品中的丙烯酰胺,用甲醇洗脱,洗脱液用FID测定,方法回收率为831~990%,相对标准偏差为534%,检出限为0016mg/L。 相似文献
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气相色谱法测定工业废气中的异丙醇 总被引:1,自引:1,他引:0
用活性炭吸附管采集吸附工业废气中的异丙醇,经二硫化碳解析后由自动进样器送入气相色谱仪中分离并由FID检测器检测。2 mL二硫化碳解吸溶剂中异丙醇的绝对量为1.57~6.28 mg时,测定结果的相对标准偏差为2.4%~7.6%(n=5);当样品采集量为10 L时,方法检出限为0.3 mg/m3。所用活性炭采样管对异丙醇的吸附效果良好,100 mg活性炭对异丙醇的穿透容量大于15 mg;二硫化碳溶剂对吸附在活性炭中的异丙醇解吸效果较好,异丙醇加标量为3.92~15.70 mg时,解吸效率为93.9%~100.5%。 相似文献
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在环境监测中,挥发酚的测定常采用4-氨基安替比林(4—AAP)—氯仿萃取比色法,此法灵敏度高,稳定性好。但由于4—AAP试剂易被氧化,使测酚的空白值较大,以致影响样品的测定。本文提出用氯仿对4—AAP试剂进行萃取来降低测酚空白值,并与用活性炭对4—AAP试剂吸附脱色做了对比,实验结果表明:此方法在许多方面都优于活性炭吸附脱色法。 相似文献
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用红外分光光度法测定样品中石油类时,四氯化碳(CCl4)的纯度对测定结果有影响,必须先提纯CCl4,使其纯度满足方法要求.常用的提纯方法有吸附法、水浴蒸馏法、混合精制法和酸化法,但这些提纯方法成本高,效率低,甚至在提纯过程中还会引入其他杂质,先蒸馏CCl4,再将蒸馏后的CCl4利用活性炭吸附,是精制CCl4的好方法. 相似文献
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改进的还原偶氮光度法同时快速测定水中硝基苯和苯胺 总被引:1,自引:1,他引:0
对测定方法进行了改进,建立了用还原-偶氮分光光度法同时快速测定水中硝基苯和苯胺的分析方法。根据实验原理,对样品前处理装置进行了改进,实验步骤得到了简化,避免了样品溶液过滤转移过程造成样品损失,使样品前处理实验效率提高了90%以上;改进后的测定方法不仅可快速测定样品中硝基苯,还可同时测定样品中苯胺;达到了用一种分析方法同时测定样品中两种污染物的目的。方法精密度测定结果,相对标准偏差(n=6,RSD)为1.9%~3.2%;对硝基苯、苯胺混合标准样品以及实际废水样品进行了测定,并与原测定方法及苯胺国标测定方法进行了比对实验;测定结果具有一致性。加标实验回收率为96%~101%,表明方法准确可靠,可用于水和废水中硝基苯或硝基苯和苯胺的同时测定。 相似文献
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建立微库仑滴定法测定水质中可吸附有机卤素AOX的方法,考察3种活性炭柱对于空白的影响。实验结果表明,AOX的检出限为2.19μg/L,相对标准偏差为2.80%,纯水中高、中、低加标回收率在92.5%~107%,新疆棉浆粕企业废水中加标回收率为96.0%~101%。实验室空白也只有新购开封的耶拿原装活性炭小柱能满足标准要求的空白值(<30μg/L)。 相似文献
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采用活性炭吸附气体样品中的丙烯酸甲酯,用二硫化碳浸泡解吸30 min后,取上清液进样,用气相色谱法FID检测器测定。方法在0.475 mg/L~38.0 mg/L范围内线性良好,空白活性炭采样管的3个浓度水平加标回收率为94.7%~98.7%,测定结果的RSD为2.7%~4.6%,方法检出限为0.075μg,当采集1.5 L气体样品时,最低检测质量浓度为0.05 mg/m3。以南京化学工业园区常见的15种化合物做干扰试验,结果方法稳定性好,测定不受干扰。用该方法测定南京市某企业周边环境空气,结果上风向和下风向丙烯酸甲酯均未检出。 相似文献
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针对目前室内环境监测工作出现的种种问题,就如何规范的开展室内环境监测工作,更好地为社会提供真实、准确、有效的监测数据,本文提出相关的探讨。 相似文献
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Peter Timmerman 《Environmental monitoring and assessment》1998,49(2-3):111-122
The social and economic implications of atmospheric change on biodiversity need to be seen in a global context of major shifts in the conceptualization and management of our relationship with nature. Traditionally, we have conceptualized the atmosphere and the other creatures of the biosphere as separate from the human, but their quasi-autonomy is now becoming subject to more and more human management. This raises not only economic issues, but social, political, and ethical concerns that will have substantial influence on public policy. Among these are the commodification of genetic material; the privatization of traditional knowledge; and the management of information. In this broader context, the paper examines an array of current and proposed strategies of response to changes in biodiversity as a result of climatic and other stresses. 相似文献
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Canada responded to the Global Biodiversity Convention by completing the Canadian Biodiversity Strategy in 1995. At the same time, Environment Canada also completed a national Science Assessment on Biodiversity. During this period, the Smithsonian Institution, in partnership with Parks and Environment Canada, initiated the implementation of a global biodiversity monitoring program in Canada. Under the auspices of the United Nations Man and the Biosphere Program, the SI/MAB monitoring protocols and plots have spread across Canada at an unprecedented rate. National champions in the science and educational sectors, working within an inter-disciplinary ecological framework, have guided the development, education, quality control and sharing of atmosphere-biodiversity observations electronically.Atmospheric-Biodiversity Networks and Networking have traditionally operated within separate mandates with little degree of integration. Air-Bio Networks were designed within an integrated framework to better understand the atmospheric stress on biodiversity and the adaptation actions, nationally and regionally. Detailed examples of the cumulative effects of climate change, stratospheric ozone depletion, acid deposition, ground-level ozone, suspended particulate matter and hazardous air pollutants on biodiversity will be discussed using a Southern Ontario case study. In addition, recommendations will be presented for future paired SI/MAB plots, linked networks and networking for adaptation within the context of climate, chemical and ecological gradients. 相似文献
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Xiangyun Liu Yan Yang Ying Cui Huijun Zhu Xiong Li Zhining Li Kankan Zhang Deyu Hu 《Environmental monitoring and assessment》2014,186(8):5307-5313
A simple and accurate method of determining metalaxyl and cymoxanil in pepper and soil was developed by ultra-performance liquid chromatography–photodiode array detection. The limits of detection were 0.015 mg/kg for metalaxyl and 0.003 mg/kg for cymoxanil. The limits of quantification were 0.05 mg/kg for metalaxyl in pepper and soil as well as 0.01 mg/kg for cymoxanil in pepper and soil. Recoveries of pepper and soil were investigated at three spiking levels and ranged within 77.52 to 102.05 % for metalaxyl and 87.15 to 103.21 % for cymoxanil, with relative standard deviations below 9.30 %. For field experiments, the half-lives of metalaxyl were 3.2 to 3.9 days in pepper and 4.4 to 9.5 days in soil at the three experimental locations in China. At harvest, pepper samples were found to contain metalaxyl and cymoxanil well below the maximum residue limit MRLs of the European Union (EU) following the recommended dosage and the interval of 21 days after last application. 相似文献
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Junxue Wu Hongyan Zhang Kai Wang Chengju Wang 《Environmental monitoring and assessment》2014,186(2):1195-1202
A simple and accurate method for the determination of bismerthiazol and its metabolite 2-amino-5-mercapto-1,3,4-thiadiazole was developed in Chinese cabbage and soil by high-performance liquid chromatography-diode array detection in this study. The limits of detection were 0.06 mg/kg for bismerthiazol and 0.03 mg/kg for 2-amino-5-mercapto-1,3,4-thiadiazole, respectively. Recoveries of cabbage and soil were investigated at three spiking levels and were in the range of 84.0–96.0 % for bismerthiazol and 71.0–74.6 % for 2-amino-5-mercapto-1,3,4-thiadiazole, with relative standard deviations below 7.0 %. For field experiments, the half-life of bismerthiazol was 2.4–2.5 days in Chinese cabbage and 2.5–4.8 days in soil at the two experimental locations in China. Dissipation residues of 2-amino-5-mercapto-1,3,4-thiadiazole were lower than 0.72 mg/kg. Terminal residues of bismerthiazol and its metabolite were less than 3.0 and 0.3 mg/kg in Chinese cabbage, respectively. No bismerthiazol or metabolite residues were detected in soil on days 5, 7, 10, and 14 after the last spraying at the two dosage levels. 相似文献
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Lin Wang Wenming Li Puyu Li Minghui Li Shuo Chen Lijun Han 《Environmental monitoring and assessment》2014,186(11):7793-7799
A simple residue analytical method using the quick, easy, cheap, effective, rugged, and safe (QuEChERS) procedure for the determination of trifloxystrobin and its metabolite trifloxystrobin acid (CGA321113) in tomato and soil was developed using high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). The limits of detection were 0.0005 mg/kg for trifloxystrobin and 0.001 mg/kg for trifloxystrobin acid, respectively. The average recoveries in tomato and soil ranged from 73–99 % for trifloxystrobin and 75–109 % for trifloxystrobin acid, with relative standard deviations below 15 %. The method was then used to study the dissipation and residues in tomato and soil. The dissipation half-lives of trifloxystrobin in tomato were 2.9 days (Beijing) and 5.4 days (Shandong), while in soil were 1.9 days (Beijing) and 3.0 days (Shandong), respectively. The final results showed that the major residue compound was trifloxystrobin in tomato whereas it was its metabolite, trifloxystrobin acid, in soil. The final residues of total trifloxystrobin (including trifloxystrobin acid) were below the EU maximum residue limit of 0.5 mg kg?1 in tomato 3 days after the treatment. 相似文献