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81.
82.
采用顶空气相色谱质谱(HS/GC-MS)联用技术对污泥恶臭成分进行检测,从污泥恶臭成分中分离多种化合物,并鉴定出烷、醛及苯等有机物。不同地区污泥的性质不尽相同,从而使恶臭成分也产生很大差异。HS/GC-MS法是一种分析污泥恶臭成分的有效方法,为污泥恶臭污染的防治提供了科学依据。 相似文献
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84.
建立了利用气相色谱-质谱法快速筛查气态制冷剂产品中的10种热点管控类卤代烃的分析方法。采用气密性微量注射器对气态制冷剂样品进行取样,刺透瓶盖隔垫加入到顶空瓶中,自动进样;以GS-GasPro(多孔层开管,60 m×0.32 mm)为色谱柱,采用电子轰击离子源,全扫描模式采集。测试结果显示:目标物的体积分数在0.50%~100.00%范围内,相对响应因子的相对标准偏差(RSD)均小于20%;线性相关系数r均在0.999以上;检出限(3.143倍标准偏差)为0.01%~0.05%。对实际样品进行加标回收,回收率为79.5%~102%,测定值RSD为0.5%~3.1%。该方法可为快速、准确、批量筛查气态制冷剂产品中的多种热点管控类卤代烃提供技术支撑。 相似文献
85.
Previous studies in the Douro River estuary, based on occasional sampling, showed the presence of several estrogenic disrupting chemicals (EDCs). In sequence, we hypothesized that such type of pollution was more likely an enduring issue than an occasional phenomenon, and that it may even affect recreational beaches in each side of the estuarine mouth. Thus to conclude about the continuous influx of EDCs, water samples were taken twice a day, once per a week, from March to May of 2009, at four sites within the estuary and at two sites in the coastline. After solid-phase extraction, the extracts were prepared for GC-MS analysis of 11 reference EDCs. These embraced natural and pharmaceutical estrogens (17β-estradiol, estrone and 17α-ethynylestradiol) and xenoestrogenic industrial pollutants (4-octylphenol, 4-nonylphenol, and their mono and diethoxylates and bisphenol A). Data showed the ubiquitous presence of potentially hazardous amounts of natural estrogens (particularly of estradiol, ca 5.5?ng?L?1) and persistent organic pollutants such as nonylphenol mono (up to 550?ng?L?1) and diethoxylate (up to 2000?ng?L?1). It was concluded that the targeted area is continuously polluted by the assayed EDCs, and as a consequence, conditions exist for endocrine disturbance in the biota by chronic exposure to EDCs. 相似文献
86.
In this paper, a method using solid-phase extraction (SPE) and gas chromatography-mass spectrometry (GC-MS) was developed to simultaneously analyze five taste and odor compounds in surface water, i.e., 2-methylisoborneol (2-MIB), 2,4,6-trichloroanisole (TCA), 2-isopropyl-3-methoxy pyrazine (IPMP), 2-isobutyl-3-methoxy pyrazine (IBMP), and trans -1,10-dimethyl-trans -9-decalol (geosmin, GSM). The mass spectrometry was operated in selective ion monitoring (SIM) mode. Three kinds of SPE columns and three eluting solvents were compared, the C18 column was chosen as optimum SPE column, and methanol was chosen as the optimum eluting solvent. It was found that the method showed good linearity in the range of 1–200 ng·L-1 and gave detection limits of 0.5–1.5 ng·L-1 for individual compounds. Good recoveries (93.5%–108%) and relative standard deviations (1.58%–7.31%) were also obtained. Additionally, concentrations of these taste and odor compounds in Jinan’s surface and drinking water were analyzed by applying this method, and the results showed that GSM and 2-MIB were the dominant taste and odor compounds in Jinan’s raw water. 相似文献
87.
某癌症高发区水中多环芳烃测定及其风险评价 总被引:2,自引:1,他引:1
在某癌症高发区选取5个镇中的10个村进行布点,分别在2010年6月和12月采集丰水期和枯水期水样,采用固相萃取与气相色谱-质谱联用方法对深层地下水、浅层地下水以及地表水中的多环芳烃(PAHs)进行测定.检测结果表明,深层地下水在丰、枯水期时PAHs总量分别为4058.29—9613.53 ng.L-1和72.78—809.00 ng.L-1.浅层地下水丰、枯水期PAHs总量分别为2205.84—24621.20 ng.L-1和82.88—601.95 ng.L-1.地表水丰、枯水期PAHs的总量分别为2747.44—33532.90 ng.L-1和127.78—321.04 ng.L-1.丰水期萘含量较高是造成PAHs总量在丰水期远高于枯水期的主要原因.10个水样中苯并(a)芘超标(GB5749—2006),最大超标8.42倍.采用优化的USEPA风险评价模型,对PAHs进行人体健康风险评价,其致癌风险水平在2×10-8—1.28×10-5之间,部分水样致癌风险超过10-6的水质监控值. 相似文献
88.
89.
This study aimed to identify the difference in volatile aromatic components and the relationship with the expression pattern of their corresponding bio-synthesis genes in six kiwifruit (Actinidia chinensis) varieties (Cuiyu, Jintao, Jinyan, Chuhong, Donghong, and Xixuan). To provide a foundation for kiwifruit variety recognition, fruit quality evaluation, and molecular-assisted breeding, the volatile aromatic components in the ripe fruits of six kiwifruit varieties were evaluated by head space-solid phase micro extraction/gas chromatography-mass spectrometry. The aroma-synthesis-related genes, including acyltransferases (AcAT16), lipoxygenase (AcLox2), and terpene synthase genes (AcTPS1), were detected by the real time-quantitative polymerase chain reaction (qPCR) during the postharvest stage of fruits. Ninety-two aroma chemicals were identified in the tested kiwifruit cultivars. There were 35, 32, 30, 44, 28, and 17 of aromatic compounds in Cuiyu, Jintao, Jinyan, Chuhong, Donghong, and Xixuan, respectively. Esters were the main aroma components in Cuiyu, Jintao, and Jinyan. The major aromatic compounds of Chuhong, Donghong, and Xixuan were aldehydes and terpenoids. The expression level of AcATs16 and AcLox2 increased, and then decreased during the ripening of kiwifruit fruits. The expression of AcATs16 was significantly higher in Cuiyu and Jinyan than in other varieties. AcLox2 indicated significant abundance in Cuiyu and Chuhong. AcTPS1 was up-regulated in Jintao, Donghong, and Xixuan with fruit ripening; however, this was not observed in Cuiyu, Chuhong, and Jinyan. The difference in the composition and content of volatile aromatic components contributes to the difference in aroma in different kiwifruit cultivars. The diverse expression of AcATs16, AcLox2, and AcTPS1 might be closely related to the synthesis of ethyl butyrate, (E)-2-hexenal, and eucalyptol, respectively. © 2018 Science Press. All rights reserved. 相似文献
90.
采用吹扫捕集-气相色谱-质谱联用(PT-GC-MS)法,研究了污染土壤中苯系物(包括苯、甲苯、乙苯、对间二甲苯、邻二甲苯和异丙苯)的测定方法,优化了吹扫捕集作为北京潮土中苯系物预处理方法的参数. 结果表明,吹扫时间11 min,解吸温度190 ℃和解吸时间0.5 min为最佳的吹扫捕集方法参数. 采用PT-GC-MS法测定土壤中的苯系物的平均加标回收率为99.0%~103.9%,相对标准偏差为10.3%~17.5%(n=7);苯系物的检出限为1.6~2.8 μg/kg,定量限为5.4~9.6 μg/kg. 将研究结果与文献中的苯系物监测质量控制参数进行比较发现,由于采用有机质含量低、砂质壤土质地的北京潮土为研究对象,使该试验的回收率均高于文献中的结果;同时,相对标准偏差和检出限与文献中的结果也存在差异,主要是由于挥发性污染物所赋存的介质及实验仪器操作条件不同所致. 相似文献