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141.
142.
Mengnjo J. Wirmvem Takeshi Oh Wilson Y. Fantong Samuel N. Ayonghe Jonathan N. Hogarh Justice Y. Suil Asobo Nkengmatia E. Asaah Seigo Ooki Gregory Tanyileke Joseph V. Hell 《环境科学学报(英文版)》2014,26(4):801-809
Rainwater characteristics can reveal emissions from various anthropogenic and natural sources into the atmosphere. The physico-chemical characteristics of 44 monthly rainfall events (collected between January and December 2012) from 4 weather stations (Bamenda, Ndop plain, Ndawara and Kumbo) in the Bamenda Highlands (BH) were investigated. The purpose was to determine the sources of chemical species, their seasonal inputs and suitability of the rainwater for drinking. The mean pH of 5 indicated the slightly acidic nature of the rainwater. Average total dissolved solids (TDS) were low (6.7 mg/L), characteristic of unpolluted atmospheric moisture/air. Major ion concentrations (mg/L) were low and in the order K+ 〉 Ca2+ 〉 Mg2~ 〉 Na+ for cations and NO3 〉〉 HCO3 〉 SO] 〉 CI- 〉 PO3- 〉 F- for anions. The average rainwater in the area was mixed Ca-Mg-SO4-CI water type. The CI-/Na+ ratio (1.04) was comparable to that of seawater (1.16), an indication that N a+ and CI originated mainly from marine (Atlantic Ocean) aerosols. High enrichments of Ca2+, Mg2+ and SO2- to Na+ ratios relative to seawater ratios (constituting 44% of the total ions) demonstrated their terrigenous origin, mainly from Saharan and Sahelian arid dusts. The K+/Na+ ratio (2.24), which was similar to tropical vegetation ash (2.38), and NO3 was essentially from biomass burning. Light (〈 100 mm) pre-monsoon and post-monsoon convective rains were enriched in major ions than the heavy (〉 100 mm) monsoon rains, indicating a high contribution of major ions during the low convective showers. Despite the acidic nature, the TDS and major ion concentrations classified the rainwater as potable based on the WHO guidelines. 相似文献
143.
Ibrahima Sow Robert K. Dixon Jie Pan Anil Sookdeo Evelyn Swain Laurent Granier 《Mitigation and Adaptation Strategies for Global Change》2014,19(1):93-106
Persistent Organic Pollutants (POPs) threaten human health and the global environment. Recognizing their dangers many countries began to limit or ban POPs production, use, and release in the 1990s. Eventually the Stockholm Convention on POPs, was adopted in 2001 and entered into force in 2004. The Global Environment Facility (GEF) provides financial support to developing country Parties for the implementation of the Stockholm Convention. The GEF’s POPs investment portfolio focuses on: 1) strengthening the capacity of developing country Parties to implement the Stockholm Convention; 2) establishing and supporting partnerships to develop and implement National Implementation Plans (NIPs), and 3) demonstrating and deploying best technologies and practices to reduce POPs emission, including development of safe alternatives. Since 2001 the GEF has committed US$568.8 million to POPs projects and leveraged some US$1474.5 million in co-financing from partners in the public and private sectors, bringing the total value of the GEF POPs portfolio to over US$2 billion. With GEF support, 108 developing country Parties have developed their NIPs. The GEF also financed 109 projects for the implementation of the Convention. Upon completion, these GEF POPs investments will contribute to the disposal of more than 70,000 tons of Polychlorinated Biphenyls (PCBs) oil, contaminated equipments, and waste, more than 40,000 tons of obsolete POPs pesticides and associated waste, and reducing dioxin/furan and mercury emission by introducing environmentally sound technologies and best practices. This paper summarizes: 1) direct and indirect GEF investments to support the goals of the Stockholm Convention; 2) investment case studies on PCB, DichloroDiphenylTrichloroethane (DDT), chlordane and mirex, medical waste, obsolete POPs and engaging civil society; and 3) lessons learned in terms of GEF financing strategies, best technologies and environmental practices to address POPs. 相似文献
144.
改性氢氧化镁制备及其去除地下水中Cr3+性能研究 总被引:1,自引:0,他引:1
氢氧化镁作为一种可缓慢释放OH-的碱,能使多数重金属离子转换为沉淀,而且不会引起太大的pH变化.但氢氧化镁难溶于水,在含水层中的迁移能力很差.若要用于地下水重金属污染修复,需要对氢氧化镁进行改性.因此,本文利用表面活性剂对氢氧化镁粉末进行改性,合成了氢氧化镁胶体,并对改性氢氧化镁的稳定性、粒度及其对Cr3+的稳定化效果进行了分析.结果表明,复配表面活性剂改性的氢氧化镁悬浮液稳定性好,粒径小,0.6~8.4μm的颗粒占82.41%.利用改性氢氧化镁对Cr3+污染地下水进行处理,其对Cr3+的去除机理主要为沉淀反应,氢氧化镁和Cr3+反应的质量比约为1.333∶1,氢氧化镁和初始Cr3+浓度对Cr3+的去除效果都有较大的影响. 相似文献
145.
146.
生态环境变化遥感评价指数的应用研究——以敖江流域为例 总被引:1,自引:0,他引:1
利用1994年5月12日与2009年6月6日的Landsat TM和2001年5月23日的Landsat ETM+卫星影像,选用遥感生态指数(RSEI),结合流域的植被覆盖度状况,定量评价了15年间敖江流域的生态环境变化与植被覆盖度变化情况,并对二者的关系进行了简要分析.结果表明:15年间,敖江流域生态等级为优所占的面积比例从13.48%上升到24.90%,增加了304.29 km2;植被覆盖度等级为极高的面积增加比例为29.31%.总体看来,敖江流域生态环境状况和植被覆盖状况均有明显的提高,两者具有较好的对应关系. 相似文献
147.
磁性氮掺石墨烯活化过硫酸钾降解水中亚甲基蓝 总被引:1,自引:0,他引:1
活化过硫酸盐产生硫酸根自由基的高级氧化技术在水环境污染物治理中引起了广泛的关注和研究.本研究采用水热法制备磁性氮掺石墨烯(M-N-G)作为催化剂.利用SEM、BET、XRD和VSM等手段表征材料,系统研究了该材料活化过硫酸盐降解亚甲基蓝的效能.结果表明:M-N-G的比表面积为94.35 m2·g-1,磁性Fe3O4分布在材料表面,能有效的活化过硫酸钾降解亚甲基蓝.当催化剂的用量为200 mg·L~(-1),过硫酸钾浓度为0.4~0.5 mmol·L~(-1)时,在p H=3~6时对10 mg·L~(-1)亚甲基蓝的降解率达90%以上.体系温度在15~32℃时,降解速率常数在0.0227~0.0488 min-1,反应活化能为33.7 k J·mol-1.EPR分析及自由基漼灭实验证明了体系中有羟基自由基和硫酸根自由基产生.TOC分析结果表明:TOC去除率可达50%.M-N-G经过简单的稀硫酸和水洗后,可高效重复利用4次.该技术方法简单、高效、无二次污染,能为有机污染物废水处理提供一种新的方法选择. 相似文献
148.
149.
Health risks of heavy metals in contaminated soils and food crops irrigated with wastewater in Beijing, China 总被引:24,自引:0,他引:24
Khan S Cao Q Zheng YM Huang YZ Zhu YG 《Environmental pollution (Barking, Essex : 1987)》2008,152(3):686-692
Consumption of food crops contaminated with heavy metals is a major food chain route for human exposure. We studied the health risks of heavy metals in contaminated food crops irrigated with wastewater. Results indicate that there is a substantial buildup of heavy metals in wastewater-irrigated soils, collected from Beijing, China. Heavy metal concentrations in plants grown in wastewater-irrigated soils were significantly higher (P相似文献
150.
Seasonal concentrations and partitioning of PAHs in a suburban site of Bursa, Turkey 总被引:3,自引:0,他引:3
Effects of space heating on atmospheric concentrations and gas-particle partitioning of PAHs were investigated in a suburban site of Bursa, Turkey. The average concentrations of ∑15-PAHs in heating season samples were approximately 10 times higher than those of non-heating season samples. The plot of log Kp versus log PL0 for all the data set gave significantly different slopes. The slope for the heating season (−0.75) samples was steeper than the one for the non-heating season (−0.64) samples. It was also observed that partitioning of PAHs for the non-heating season samples showed different characteristics depending on air parcel trajectories. Generally steeper slopes were obtained for the air parcels traveled across the Black sea and arrived to the sampling site from northern sector. On the other hand, the variations in slopes according to air mass origin were insignificant for the heating season samples. Local contributions from space heating are the reason for this observation. 相似文献