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31.
High-surface-area mesoprous powders of γ-Al2O3 doped with Cu2 +, Cr3 +, and V3 + ions were prepared via a modified sol–gel method and were investigated as catalysts for the oxidation of chlorinated organic compounds. The composites retained high surface areas and pore volumes comparable with those of undoped γ-Al2O3 and the presence of the transition metal ions enhanced their surface acidic properties. The catalytic activity of the prepared catalysts in the oxidation of 1,2-dichloroethane (DCE) was studied in the temperature range of 250–400°C. The catalytic activity and product selectivity were strongly dependent on the presence and the type of dopant ion. While Cu2 +- and Cr3 +-containing catalysts showed 100% conversion at 300°C and 350°C, V3 +-containing catalyst showed considerably lower conversion. Furthermore, while the major products of the reactions over γ-alumina were vinyl chloride (C2H3Cl) and hydrogen chloride (HCl) at all temperatures, Cu- and Cr-doped catalysts showed significantly stronger capability for deep oxidation to CO2. 相似文献
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33.
Carbonyl compounds are important intermediates in atmospheric photochemistry, but their primary sources are still not understood well. In this work, carbonyls, hydrocarbons, and alkyl nitrates were continuously measured during November 2011 at a rural site in the Yangtze River Delta region of China. Mixing ratios of carbonyls and hydrocarbons showed large fluctuations during the entire measurement. The average level for total measured volatile organic compounds during the pollution episode from 25th to 27th November, 2011 was 91.6 ppb, about 7 times the value for the clean period of 7th-8th, November, 2011. To preliminarily identify toluene sources at this site, the emission ratio of toluene to benzene (T/B) during the pollution episode was determined based on photochemical ages derived from the relationship of alkyl nitrates to their parent alkanes. The calculated T/B was 5.8 ppb/ppb, significantly higher than the values of 0.2-1.7 ppb/ppb for vehicular exhaust and other combustion sources, indicating the dominant influence of industrial emissions on ambient toluene. The contributions of industrial sources to ambient carbonyls were then calculated using a multiple linear regression fit model that used toluene and alkyl nitrates as respective tracers for industrial emission and secondary production. During the pollution episode, 18.5%, 69.0%, and 52.9% of measured formaldehyde, acetaldehyde, and acetone were considered to be attributable to industrial emissions. The emission ratios relative to toluene for formaldehyde, acetaldehyde, and acetone were determined to be 0.10, 0.20 and 0.40 ppb/ppb, respectively. More research on industrial carbonyl emission characteristics is needed to understand carbonyl sources better. 相似文献
34.
有机气溶胶的来源与形成研究现状 总被引:8,自引:3,他引:8
介绍了有机气溶胶来源与形成的研究现状,从有机气溶胶的化学组成特征、一次有机气溶胶的来源和二次有机气溶胶的形成机制论述其研究进展.一次有机气溶胶主要来源于烹调油烟、机动车排放、生物质燃烧、工业或民用燃油锅炉释放出的有机物,还有道路扬尘、沥青、刹车尘、轮胎屑、室外香烟烟雾、以及高等植物蜡、细菌活动和草本植物等.大气中的半挥发性有机物可通过物理和化学吸附形成二次有机气溶胶,一些挥发性有机物可通过气相化学反应转化为低挥发性的物质并形成二次有机气溶胶,其主要前体物是芳香族化合物,如苯、甲苯、二甲苯,以及烯烃、烷烃、环烷烃、萜烯和生物排放的非饱和氧化物. 相似文献
35.
为及时、准确掌握黑臭水体治理进展,基于“北京二号”影像数据和同期的野外综合水体实测数据,采用深度学习算法对黑臭水体进行识别,并引入地理探测器对黑臭水体影响因素进行定量分析。结果表明:基于Faster R-CNN算法的黑臭水体遥感识别,总准确率达到90%左右,短时间内(5~33 h)即可完成北京市建成区黑臭水体的筛查工作;在空间维度上,黑臭水体主要分布在中心城区以外,并在通州区、朝阳区和大兴区较为集中;在时间维度上,专项治理期间(2015—2018年)内,黑臭水体的数量和长度总体趋势都是递减的,但偶尔也有反黑现象;2018年底,在全市建成区范围内,已全面消除黑臭现象;在一年内,第1季度水体环境最好,第2季度次之,第3季度最差,从第4季度开始好转;在北京市大兴区,土壤全氮量(贡献率为32.07%)和周边养殖场排污(贡献率为27.04%)是黑臭水体形成的主要影响因素,高程(贡献率为8%)、土壤类型(贡献率为7.6%)和土地利用类型(贡献率为6.1%)的贡献率较弱。由此可以看出,基于Faster R-CNN算法识别影像中的黑臭水体识别准确率高,可及时、准确地监测城市黑臭水体治理情况,使用地理探测器可定量分析并确定各影响因素的贡献率。本研究成果可为城市黑臭水体的动态监测和治理提供有力的技术支撑。 相似文献
36.
采集了上海地区8家不同类型的涂料制造企业中不同生产环节有组织排放的废气样本,分析其VOCs组分特征和活性VOCs物种,并应用3种实际排放量核算方法计算企业的VOCs年排放量,分析了其与排污许可排放量的关系。结果表明:1)涂料制造行业排放废气的特征组分为芳香烃、OVOCs、卤代烃,占全部VOCs质量浓度的56.2%~99.1%,乙酸乙酯、乙酸丁酯、4-乙基甲苯、间/对二甲苯、甲苯、甲乙酮是涂料制造行业VOCs排放的典型物种;2)基于MIR值法的计算结果,芳香烃和OVOCs是涂料制造行业排放VOCs的主要活性组分,累计OFP贡献率达36.0%~99.8%,其中,4-乙基甲苯(52.1%)、氯乙烯(48.1%)、乙酸丁酯(47.9%)、乙酸乙酯(42.6%)、间/对二甲苯(41.3%)是各类涂料工艺废气中OFP贡献率最高的物质,除苯系物、乙酸酯类化合物外,氯乙烯、甲乙酮、四氢呋喃也是涂料制造过程中值得关注的活性物质;3)涂料制造企业车间的有组织废气VOCs排放量占全厂VOCs排放量的75.0%以上,其次是实验室废气,VOCs排放量为3.5%~16.8%。在VOCs实际排放量核算中,使用实测法的核算结果与物料衡算法接近,且计算简便,在正常运行时均低于许可排放限值;而产污系数法所核算数值较许可排放限值更高,在现阶段可作为一项惩罚性计算方法。 相似文献
37.
38.
采用磁絮凝-吸附技术开展了同步去除黑臭水体浊度、氨氮和总磷(TP)实验。在磁絮凝阶段,通过聚合硫酸铁(PFS)、磁粉(MPs)和聚丙烯酰胺(PAM)复配使用,利用电荷中和作用去除浊度和TP;同时,利用化学吸附沉淀去除TP;在此阶段中,当PFS、MPs、PAM的投加量分别为16.00、100.00、2.20 mg·L−1且以PFS+MPs在快速阶段先投加,PAM在慢速阶段后投加的顺序投配时,絮凝效果达到最佳。在吸附阶段,吸附剂质化壳聚糖-沸石(PCZ)主要通过离子交换作用去除氨氮以及通过静电吸附作用去除TP;当PCZ的投加量为1.25 g·L−1时吸附效果达到最佳。利用所研究的磁絮凝-吸附技术对实际黑臭水体进行处理,其出水浊度能达到城镇污水处理厂污染物排放一级标准(≤10.00 NTU),TP和氨氮也分别能满足地表水环境质量Ⅲ类标准(≤0.20 mg·L−1)和Ⅴ类标准(≤2.00 mg·L−1)要求。 相似文献
39.
Determination of Q1, an unknown organochlorine contaminant, in human milk, Antarctic air, and further environmental samples 总被引:2,自引:0,他引:2
Vetter W Alder L Kallenborn R Schlabach M 《Environmental pollution (Barking, Essex : 1987)》2000,110(3):6188-409
Q1, an organochlorine component with the molecular formula C(9)H(3)Cl(7)N(2) and of unknown origin was recently identified in seal blubber samples from the Namibian coast (southwest of Africa) and the Antarctic. In these samples, Q1 was more abundant than PCBs and on the level of DDT residues. Furthermore, Q1 was more abundant in seals from the Antarctic than the Arctic. To prove this assumption, gas chromatography-electron-capture negative ion mass spectrometry (GC/ECNI-MS), which is sensitive and selective for Q1, allowed for screening of traces of Q1 even in samples with particularly high levels of other organochlorine contaminants. Q1 was isolated by high-performance liquid chromatography (HPLC) from a skua liver sample. A 1:1 mixture with trans-nonachlor in electron-capture detectors (ECDs) was used to determine the relative response factor with ECNI-MS. The ECNI-MS response of Q1 turned out to be 4.5 times higher than that of trans-nonachlor in an ECD. With GC/ECNI-MS in the selected ion-monitoring mode, four Antarctic and four Arctic air samples were investigated for the presence of Q1. In the Antarctic air samples, Q1 levels ranged from 0.7 to 0.9 fg/m(3). In Arctic air samples, however, Q1 was below the detection limit (<0.06 fg/m(3) or 60 ag/m(3)). We also report on high Q1 levels in selected human milk samples (12-230 microg/kg lipid) and, therefore, suggested that the unknown Q1 is an environmental compound whose origin and distribution should be investigated in detail. Our data confirm that Q1 is a bioaccumulative natural organochlorine product. Detection of a highly chlorinated natural organochlorine compound in air and human milk is novel. 相似文献
40.