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851.
通过对新、旧2种折弯机组合上模从工艺结构、受力分析、设计要点及调节使用等方面进行全面的比较和分析,提出一种新的、合理的上模结构——偏心销式分段有量度调节结构的折弯机组合上模. 相似文献
852.
为实施流域水资源有效保护,从技术管理层面分析流域水资源共享过程中标准体系的构成与作用。对现阶段实施的生活饮用水卫生标准、地表水环境质量标准和排水标准中涵盖的有机污染物进行对称性分析,指出标准体系中存在的技术风险以及生活污水和工业废水混排存在的管理风险。以松花江流域中某化工厂排水为实例进行有机污染物成份检测,发现了标准体系对污染物监控存在的疏漏。提出从人体健康角度完善排水和水环境质量标准,从流域水资源共享角度对排水和给水设施进行整体规划和布局,从水资源安全保障角度建立流域有机污染物优先控制名单。 相似文献
853.
电离辐射防护不仅要保护人类而且要保护非人类生物,这是辐射防护概念的一个重大变化,也是生态保护的一大重要举措。本文概述了欧盟生物辐射剂量评价方法 FASSSET的框架体系结构、参考生物和剂量学模型。本文以某内陆核电厂为例,采用ERICA方法对该核电厂水生生物的辐射影响进行了预测计算。计算结果表明,该内陆核电厂2台百万千瓦级核电机组正常运行时对水生生物的辐射剂量率低于国际组织推荐的400μGy.h-1控制限值和ERICA的筛选剂量值10μGy.h-1。因此,该内陆核电厂不会对厂址附近水域水生生物造成不利影响。ERICA方法可作为中国现阶段开展生物辐射剂量评价的推荐方法。 相似文献
854.
Despite recent efforts to investigate the distribution and fate of polycyclic aromatic hydrocarbons (PAHs) in air, water, and soil, very little is known about their temporal change in wet deposition. As a result of increased attention to public health, a large-scale survey on the deposition flux and distribution of PAH contamination in rainwater was urgently conducted in Shanghai, China. In this study, 163 rainwater samples were collected from six sites, and 15 PAH compounds were detected by the use of a simple solid phase microextraction (SPME) technique coupled with gas chromatography-mass spectrometry. The dominant PAH species monitored were naphthalene, phenanthrene, anthracene, and fluoranthene. The concentration of total PAHs per event was between 74 and 980 ng/L, with an average value of 481 ng/L, which is at the high end of worldwide figures. The annual deposition flux of PAHs in rainwater was estimated to be 4148 kg/yr in the Shanghai area, suggesting rainfall as a major possible pathway for removing PAHs from the atmosphere. Diagnostic analysis by the ratios of An/178 and Fl/Fl+Py suggested that combustion of grass, wood, and coal was the major contributor to PAHs in the Shanghai region. Back trajectory analysis also indicated that the pollutant sources could be from the southern part of China. 相似文献
855.
以某电解锰工艺末端铬钝化废水为研究对象,采用氧化、除杂、反应制得成品,污水达标处理及回用的组合工艺,制备达到国家标准的中铬黄产品,以实现铬的回收利用。结果表明:对于H2O2氧化工艺,选用V(水样)/V(30%H2O2)为(600~1000):1;可采取加碱沉淀Mn的工艺去除杂质金属离子;铬酸铅的生成反应适宜温度为55~60℃,硝酸铅投加量为理论值的1.05倍~1.10倍;采取加石灰调pH、投加硫酸铝的方法可去除水样中剩余铅离子,V(上清液)/V(5%硫酸铝溶液)为1000~2000较合适;生产该产品基本上能够做到保本、微利,但具有显著的环境效益和社会效益。 相似文献
856.
857.
采用序批式活性污泥法(Sequencing Batch Reactor,SBR),通过接种絮状污泥研究逐级改变进水组成(配水与实际生活污水的比例)实现好氧颗粒污泥快速培养,同时考查了好氧颗粒污泥培养过程中颗粒污泥的物理性质及对污染物的去除效果。结果表明:在好氧颗粒污泥培养初期通过添加营养物质并逐渐增加实际生活污水的比例可以实现好氧颗粒污泥的快速培养,与完全用配水培养的好氧颗粒污泥基本相似,且培养出的好氧颗粒污泥结构密实,湿密度为1.046 g/cm3,比重为1.025,平均沉降速度为38.67 m/h,粒径在1 mm左右,颜色为黄褐色;同时培养的颗粒污泥对污染物有较好的处理效果,COD、NH+4-N的去除率分别高达85%、90%。培养初期在实际生活污水中通过添加营养物质能够诱导好氧颗粒污泥形成,实现好氧颗粒污泥的快速培养。 相似文献
858.
The present work aims to ascertain the mechanisms of surfactant (dodecylbenzene sulfonate; DBS) effects on the aggregation behaviors of TiO2 nanoparticles (TiO2-NPs) in natural water samples. Aggregation experiments were conducted at a TiO2-NPs concentration of 10 mg/L in deionized water and in natural water samples via dynamic light scattering and Zeta potential determination. Average attachment efficiency was calculated to compare the aggregation behaviors of nanoparticles in the two aqueous media. Results showed that the effects of DBS on aggregation could be interpreted by both Derjaguin–Landau–Verwey–Overbeek (DLVO) and non-DLVO mechanisms. In natural water samples, aggregation did not occur rapidly and was able to develop slowly under all conditions, and the roles of DBS were obvious at high DBS concentration owing to the impacts of inherent components of natural water samples, such as colloids and natural organic compounds. Future aggregation studies should concentrate on multi-factor, multi-colloidal and dynamic aspects under similar environmental conditions. 相似文献
859.
针对地面监测点位过少,不能满足大区域范围土壤酸沉降通量研究需求的现状,建立了基于OMI痕量气体遥感数据和地面观测数据的区域酸沉降通量估算方法,并对青岛市硫元素和氮元素沉降通量进行了估算。结果表明,新方法能够实现大区域范围土壤酸沉降通量的估算。与传统估算方法相比,新方法采用大气痕量气体遥感监测数据,是对酸沉降通量常规研究手段的有益补充。 相似文献
860.
Chemical and optical properties of aerosols and their interrelationship in winter in the megacity Shanghai of China 总被引:2,自引:0,他引:2
Tingting Han Liping Qiao Min Zhou Yu Qu Jianfei Du Xingang Liu Shengrong Lou Changhong Chen Hongli Wang Fang Zhang Qing Yu Qiong Wu 《环境科学学报(英文版)》2015
A field campaign on air quality was carried out in Shanghai in winter of 2012. The concentrations of NO, NO2, NOx, SO2, CO, and PM2.5 increased during haze formation. The average masses of SO42-, NO3- and NH4+ were 10.3, 11.7 and 6.7 μg/m3 during the haze episodes, which exceeded the average (9.2, 7.9, and 3.4 μg/m3) of these components in the non-haze days. The mean values for the aerosol scattering coefficient (bsp), aerosol absorption coefficient (bap) and single scattering albedo (SSA) were 288.7, 27.7 and 0.91 Mm-1, respectively. A bi-peak distribution was observed for the mass concentrations of CO, NO, NO2, and NOx. More sulfate was produced during daytime than that in the evening due to photochemical reactions. The mass concentration of NH4+ achieved a small peak at noontime. NO3- showed lower concentrations in the afternoon and higher concentrations in the early morning. There were obvious bi-peak diurnal patterns for bsp and bap as well as SSA. bsp and bap showed a positive correlation with PM2.5 mass concentration. (NH4)2SO4, NH4NO3, organic mass, elemental carbon and coarse mass accounted for 21.7%, 19.3%, 31.0%, 9.3% and 12.3% of the total extinction coefficient during non-haze days, and 25.6%, 24.3%, 30.1%, 8.1% and 8.2% during hazy days. Organic matter was the largest contributor to light extinction. The contribution proportions of ammonium sulfate and ammonium nitrate to light extinction were significantly higher during the hazy time than during the non-haze days. 相似文献