首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   483篇
  免费   35篇
  国内免费   120篇
安全科学   36篇
废物处理   28篇
环保管理   36篇
综合类   249篇
基础理论   87篇
污染及防治   143篇
评价与监测   22篇
社会与环境   15篇
灾害及防治   22篇
  2023年   5篇
  2022年   25篇
  2021年   17篇
  2020年   13篇
  2019年   15篇
  2018年   19篇
  2017年   27篇
  2016年   18篇
  2015年   23篇
  2014年   30篇
  2013年   66篇
  2012年   39篇
  2011年   44篇
  2010年   45篇
  2009年   29篇
  2008年   40篇
  2007年   29篇
  2006年   30篇
  2005年   16篇
  2004年   12篇
  2003年   13篇
  2002年   9篇
  2001年   11篇
  2000年   17篇
  1999年   7篇
  1998年   5篇
  1997年   7篇
  1996年   4篇
  1995年   7篇
  1994年   2篇
  1993年   5篇
  1992年   1篇
  1991年   3篇
  1990年   2篇
  1987年   1篇
  1984年   1篇
  1976年   1篇
排序方式: 共有638条查询结果,搜索用时 15 毫秒
11.
李乃文  冀永红  刘孟潇  牛莉霞 《安全》2019,40(9):26-34,5
为减少矿工怠工行为,基于24Model研究矿工怠工行为的管理模式架构及策略。首先,基于冰山模型理论分析矿工怠工行为的影响因素;其次,基于24Model和行为修正理论提出集怠工行为识别、行为原因分析、行为管理策略选择和行为修正评估于一体的矿工怠工行为管理模式架构;最后,提出了针对性的管理策略。对于提高煤矿企业矿工的工作绩效具有重要的理论意义和实践价值。  相似文献   
12.
The inhibition and dispersion of polyepoxysuccinate (PESA, self-manufactured) to inorganic scale was evaluated by scale static beaker test to CaC03 and Ca3(P04)2, stability test to zinc salt, and dispersion test to ferric oxide. The experimental results demonstrated that PESA functioned excellent scale inhibition to CaC03 and Ca3(P04)2, good stability to zinc salt and special dispersion to ferric oxide. Under the water with hardness 500-1200 mg/L, alkalinity 1000 mg/L, and dosage of PESA 31.2 mg/L, PESA scale inhibition ratio reached more than 85.0%. At dosage of PESA 20.8 mg/L inhibition ratio on calcium phosphate reached 38.9%, at optimum dosage of PESA 9.1 mg/L, the stability ratio was up to 96.1%; while at dosage of PESA 3.6 mg/L, transmittance ratio reached 64.4%. Therefore, PESA can be considered a soluble, high effective and versatile inhibitor.  相似文献   
13.
为评估不同交通状态下公交车运行特征和排放水平的差异,现场采集广州市B9、226线路公交车的逐秒GPS数据,以ES-VSP(发动机负荷-机动车比功率)分布表征畅通、轻度拥堵和中度拥堵下的公交车运行特征,结合IVE(international vehicle emission)模型求得公交车平均排放因子并分析其差异.结果表明:①所测公交车的发动机低负荷区中bin11(-1.6 < ES ≤ 3.1,-2.9 kW/t ≤ VSP < 1.2 kW/t)频率范围为50.55%~83.39%,中度拥堵时bin 11频率是畅通时的1.1~1.3倍;② 3种交通状态下公交车的CO、VOC(运行产生的挥发性有机物)、VOCevap(蒸发产生的挥发性有机物)、NOx(氮氧化物)和PM(颗粒物)平均排放因子范围分别为7.63~11.40、0.26~0.46、0.68~1.56、0.32~0.51和0.72×10-2~1.28×10-2 g/km;③同种交通状态下,主干路公交车专用道和BRT车道的公交车的大部分污染物平均排放因子低于次干路混行车道、主干路混行车道,中度拥堵时主干路BRT车道的CO、VOC、VOCevap、NOx和PM平均排放因子相对其他道路最低,分别为7.66、0.27、0.87、0.32和0.75×10-2 g/km;④次干路混行车道、主干路混行车道的公交车污染物平均排放因子随交通状态愈加拥堵而增大,但畅通时主干路BRT车道的公交车行驶速度、加速度较高,导致CO平均排放因子较高,对应3种交通状态其比例为1.0:0.9:0.8.研究显示,交通状态对公交车运行和排放具有显著影响.   相似文献   
14.
Dissolved organic matter (DOM) represents one of the most mobile and reactive organic compounds in ecosystem and plays an important role in the fate and transport of soil organic pollutants, nutrient cycling and more importantly global climate change. Electrochemical methods were first employed to evaluate DOM redox properties, and spectroscopic approaches were utilized to obtain information concerning its composition and structure. DOM was extracted from a forest soil profile with five horizons. Differential pulse voltammetry indicated that there were more redox-active moieties in the DOM from upper horizons than in that from lower horizons. Cyclic voltammetry further showed that these moieties were reversible in electron transfer. Chronoamperometry was employed to quantify the electron transfer capacity of DOM, including electron acceptor capacity and electron donor capacity, both of which decreased sharply with increasing depth. FT-IR, UV-Vis and fluorescence spectra results suggested that DOM from the upper horizons was enriched with aromatic and humic structures while that from the lower horizons was rich in aliphatic carbon, which supported the findings obtained by electrochemical approaches. Electrochemical approaches combined with spectroscopic methods were applied to evaluate the characteristics of DOM extracted along a forest soil profile. The electrochemical properties of DOM, which can be rapidly and simply obtained, provide insight into the migration and transformation of DOM along a soil profile and will aid in better understanding of the biogeochemical role of DOM in natural environments.  相似文献   
15.
介绍了矿区环境影响后评估理论体系研究的重要性,构建了一条主线,一个桥梁,二个基点和二条原则的理论体系框架,并分别对理论体系的主线、系统损伤机制和系统抵御机制进行了具体分析,指出了主线理论和两大机制所涉及的具体生态/经济学原理,最后总结了矿区环境影响后评估的理论支撑体系核心机理.  相似文献   
16.
建设项目环境监理是中国环境管理制度的一个组成部分,目前尚处于试点阶段,环境监理的管理体系还有待进一步完善。在对国内环境监理工作研究之后介绍了中国环境监理产生的背景、发展历程与现状,总结了现阶段已经取得的环境监理成果,并将部分省、市、自治区的环境监理工作开展情况进行了对比;同时对国家和各级地方环保主管部门开展环境监理工作存在的不足进行了剖析并提出了一些完善环境监理制度的建议,期冀中国的环境监理制度逐步健全并在环境管理工作中发挥重要的作用。  相似文献   
17.
幸鸿  徐伟嘉  蔡铭  刘永红 《环境科学学报》2011,31(10):2102-2108
耦合微观交通仿真和机动车尾气排放模型,分别对含信号控制人行横道和不含信号控制人行横道的街道峡谷污染物排放进行计算,并以此为排放源,采用k-ε两方程模型与组分输运方程对风向与街道垂直时的污染扩散情况进行了三维数值模拟.结果表明,k-ε两方程模型与组分输运方程可以较好地模拟风向与街道垂直时三维街道峡谷内的污染物扩散情况.峡...  相似文献   
18.
Polyaspartic acid (PASP) has been extensively studied in recent years as a green scale inhibitor. PASP was synthesized by thermal polycondensation of maleic anhydride and ammonium carbonate in this study. The optimal polycondensation reaction conditions were the raw material (maleic anhydride and ammonium carbonate) molar ratio of 1.0:1.2, the polymerization temperature of 180°C and reaction time of 2.0 hr. The results showed that PASP exhibits very good scale inhibiting performance. The inhibition rate was 95% for calcium carbonate and 90% for calcium sulfate by the application of 5 mg/L PASP.  相似文献   
19.
A new type of sponge iron sphere (NSIS) with 1-5 mm diameter, made of concentrated iron powder and possessed high activity and intension, was prepared by mini-pellet sintering integrated with H2 direct reduction. Static state experiment has been carried on to investigate the Cd2+ removal efficiency from wastewater by the NSIS and to explore the Cd2+ removal reaction kinetics. It was suggested that initial pH value and Cd2+ original concentration had significant influence on Cd2+ removal percentage. Cd2+ removal percentage decreased significantly with the increasing of Cd2+original concentration whether the original pH value be adjusted to 3.0 or without adjustment. The results showed that the Cd2+ removal process followed the first order reaction because the reaction order was from 0.803 to 0.996. The apparent reaction rate constant between Cd2+ and NSIS was from 0.0025 to 0.1000 (mg·L?1)1-n·min?1. Compared with SIS reduced by charcoal reduction, NSIS deoxided by hydrogen possessed higher activity, and could remove the same quantity of Cd2+ within a shorter period of time.  相似文献   
20.
Titanium dioxide(TiO2), which is the widely used photo-catalyst, has been synthesized by simple hydrothermal solution containing tetrabutyl titanate and hydrofluoric acid. The synthesized product has been applied to photo-degradation in aqueous phase of chlorinated solvents, namely tetrachloroethene(PCE), trichloroethene(TCE) and 1,1,1-trichloroethane(TCA). The photo-degradation results revealed that the degradation of these harmful chemicals was better in UV/synthesized TiO2 system compared to UV/commercial P25 system and UV only system. The photo-catalytic efficiency of the synthesized TiO2 was 1.4, 1.8 and 3.0 folds higher compared to the commercial P25 for TCA, TCE and PCE degradation, respectively. Moreover, using nitrobenzene(NB) as a probe of hydroxyl radical(.OH), the degradation rate was better over UV/synthesized TiO2, suggesting the high concentration of.OH generated in UV/synthesized TiO2system. In addition,.OH concentration was confirmed by the strong peak displayed in EPR analysis over UV/synthesized TiO2system. The characterization result using XRD and TEM showed that the synthesized TiO2 was in anatase form and consisted of well-defined sheet-shaped structures having a rectangular outline with a thickness of 4 nm, side length of 50 nm and width of 33 nm and a surface 90.3 m2/g. XPS analysis revealed that ≡Ti-F bond was formed on the surface of the synthesized TiO2. The above results on both photocatalytic activity and the surface analysis demonstrated the good applicability of the synthesized TiO2 nano-sheets for the remediation of chlorinated solvent contaminated groundwater.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号