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991.
Constructed wetland (CW) is the preferred means of controlling water quality because of its natural treatment mechanisms and
function as a secondary or tertiary treatment unit. CW is increasingly applied in Korea for secondary e uent of livestock wastewater
treatment. This study was conducted to recognize the characteristics of contaminants in the accumulated sediment at the bottom soil
layer and to reduce the phosphorus release from sediments of the free water surface CW for the treatment of secondary piggery
wastewater e uent from a livestock wastewater treatment facility. The results revealed that the dominant phosphorus existence types
at near the inlet of the CW were non-apatite phosphorus (59%) and residual phosphorus (32%) suggesting that most of the particles of
the influent are made up of inorganic materials and dead cells. Sediment accumulation is important when determining the long-term
maintenance requirements over the lifetime of CW. Continuous monitoring will be performed for a further assessment of the CW
system and design. 相似文献
992.
Effect of sediment size on bioleaching of heavy metals from contaminated sediments of Izmir Inner Bay 总被引:7,自引:0,他引:7
The effect of sediment size on metals bioleaching from bay sediments was investigated by using fine (< 45 μm), medium (45-300 μm), and coarse (300-2000 μm) size fractions of a sediment sample contaminated with Cr, Cu, Pb, and Zn. Chemical speciation of the metals in bulk and size fractions of sediment were studied before and after bioleaching. Microbial activity was provided with mixed cultures of Acidithiobacillus thiooxidans and Acidithiobacillus ferrooxidans. The bioleaching process was carried out in flask experiments for 48 days, by using 5% (W/V) of solid concentration in suspension. Bioleaching was found to be efficient for the removal of selected heavy metals from every size fraction of sediments, where the experiments with the smaller particles resulted in the highest solubilization ratios. At the end of the experimental period, Cr, Cu, Pb and Zn were solubilized to the ratios of 68%, 88%, 72%, and 91% from the fine sediment, respectively. Higher removal efficiencies can be explained by the larger surface area provided by the smaller particles. The changes in the chemical forms of metals were determined and most of the metal releases were observed from the reducible and organic fractions independent from grain size. Higher concentrations were monitored in the residual fraction after bioleaching period, suggesting they are trapped in this fraction, and cannot be solubilized under natural conditions. 相似文献
993.
Low-carbon transition of iron and steel industry in China: Carbon intensity, economic growth and policy intervention 总被引:1,自引:0,他引:1
As the biggest iron and steel producer in the world and one of the highest CO2 emission sectors, China's iron and steel industry is undergoing a low-carbon transition accompanied by remarkable technological progress and investment adjustment, in response to the macroeconomic climate and policy intervention. Many drivers of the CO2 emissions of the iron and steel industry have been explored, but the relationships between CO2 abatement, investment and technological expenditure, and their connections with the economic growth and governmental policies in China, have not been conjointly and empirically examined. We proposed a concise conceptual model and an econometric model to investigate this crucial question. The results of regression, Granger causality test and impulse response analysis indicated that technological expenditure can significantly reduce CO2 emissions, and that investment expansion showed a negative impact on CO2 emission reduction. It was also argued with empirical evidence that a good economic situation favored CO2 abatement in China's iron and steel industry, while achieving CO2 emission reduction in this industrial sector did not necessarily threaten economic growth. This shed light on the dispute over balancing emission cutting and economic growth. Regarding the policy aspects, the year 2000 was found to be an important turning point for policy evolution and the development of the iron and steel industry in China. The subsequent command and control policies had a significant, positive effect on CO2 abatement. 相似文献
994.
以氯化铁为铁源,硼氢化钠为还原剂,壳聚糖为稳定剂,采用液相还原法制备壳聚糖稳定纳米铁(CS-nZⅥ);研究了印染废水中常见助剂NaNO3、Na2SO4、NaH2PO4、K2Cr2O7、EDTA二钠盐存在下,超声波辅助CS-nZⅥ对酸性品红(AF)降解的影响。结果表明,反应15 min,0.01 g CS-nZⅥ对25 mL、100 mg/L AF的去除率高达99.9%;各种助剂的存在使得纳米铁表面不同程度失活,阻碍反应的进行,使得AF的去除率下降。NaNO3、K2Cr2O7、EDTA二钠盐与纳米铁发生反应,与AF存在明显的竞争作用。重复利用实验表明,CS-nZⅥ重复利用7次仍具有一定的反应活性。此外,CS-nZⅥ对加标(50 mg/L)实际废水中AF的去除率达到99%以上,表明CS-nZⅥ是一种潜在的环境修复材料。 相似文献
995.
This study was performed to investigate the variables that influence chlorobenzene (CB) degradation in aqueous solution by electro-heterogeneous catalysis.The effects of current density,pH,and electrolyte concentration on CB degradation were determined.The degradation effciency of CB was almost 100% with an initial CB concentration of 50 mg/L,current density 15 mA/cm2,initial pH 10,electrolyte concentration 0.1 mol/L,and temperature 25°C after 90 min of reaction.Under the same conditions,the degradation eff... 相似文献
996.
For phosphorus (P) recovery from wastewater, the effect of humic substances (HS) on the precipitation of calcium phosphate was studied. Batch experiments of calcium phosphate precipitation were undertaken with synthetic water that contained 20 mg/L phosphate (as P) and 20 mg/L HS (as dissolved organic carbon, DOC) at a constant pH value in the range of 8.0-10.0. The concentration variations of phosphate, calcium (Ca) and HS were measured in the precipitation process; the crystalline state and compositions of the precipitates were analysed by powder X-ray diffraction (XRD) and chemical methods, respectively. It showed that at solution pH 8.0, the precipitation rate and removal efficiency of phosphate were greatly reduced by HS, but at solution pH ≥9.0, the effect of HS was very small. The Ca consumption for the precipitation of phosphate increased when HS was added; HS was also removed from solution with the precipitation of calcium phosphate. At solution pH 8.0 and HS concentrations ≤3.5 mg/L, and at pH ≥ 9.0 and HS concentrations ≤ 10 mg/L, the final precipitates were proved to be hydroxyapatite (HAP) by XRD. The increases of solution pH value and initial Ca/P ratio helped reduce the influence of HS on the precipitation of phosphate. 相似文献
997.
998.
针对国电宁夏石嘴山发电有限公司一次调频响应缓慢、调频幅度与设定值偏差较大等问题,对产生原因进行分析,提出优化方案。结果表明:数字式电液控制系统(DigitalElectronic Hydraulic control system, DEH)一次调频存在滞后环节,严重影响调频速率及调频幅度,经过参数优化后,一次调频功能满足了电网调频要求。 相似文献
999.
Changes in heavy metal contents in animal feeds and manures in an intensive animal production region of China 总被引:16,自引:0,他引:16
The 360 feed and manure samples were collected from 150 animal farms in Jiangsu Province, China and analyzed for heavy metals. Concentrations of Zn and Cu in animal feeds were 15.9-2041.8 and undetected-392.1 mg/kg respectively, while Hg, As, Pb, Cd, and Cr in all feeds were below 10 mg/kg. Concentrations of Cu, Zn, and Cr in animal manures were 8.4-1726, 39.5-11379, and 1.0-1602 mg/kg respectively, while As, Cd, Hg, and Pb were 〈 10 mg/kg. The concentration of Cu, Zn, As and Cr in animal feed and manure were positively correlated (p 〈 0.001), but the Cd, Hg, and Pb were not statistically correlated between the feed and the manure. Concentrations of Cu and Zn were highest in pig feed and manure, followed by poultry and dairy feeds and manures. During 1990- 2008, Cu, Zn, As, Cr, Cd contents increased by 771%, 410%, 420%, 220%, and 63% in pig manure, 212%, 95%, 200%, 791%, and -63% in dairy manure, and 181%, 197%, 1500%, 261, and 196% in poultry manure. Most of the increases occurred from 2002 to 2008, which reflects the extensive use of feed additives after 2002. In contrast, Pb and Hg in manures continuously decreased from 1990 to 2008. The results suggest that the heavy metal contents in animal manure have been greatly increased over 18 years and the contribution of manures to soil should be considered. 相似文献
1000.
滇黔桂地区土壤有机碳储量与影响因素研究 总被引:12,自引:1,他引:12
土壤有机碳(SOC)库在陆地生态系统中具有重要作用.由于土壤剖面数量和采用的土壤图比例尺等的限制,目前土壤有机碳库估箅尚存在很大不确定性.为了提高SOC库估算的精确性,利用798个土壤剖面及1:50万土壤图估算了滇黔桂地区(云南省、贵州省和广西壮族自治区)的SOC储量,并采用逐步回归分析和通径分析方法分析了影响SOC密度的主要因子.结果表明,滇黔桂地区表土层(0-20 cm)和土壤剖面(0-100 cm)的SOC储量分别为4.39 Pg和10.91 Pg;SOC密度分别为56.2Mg·hm-2和139.8 Mg·hm-2.高于全国平均水平.环境因子(海拔、经度、纬度、气温和降雨)、成土母质和土地利用方式对表土层和土壤剖面SOC密度变异性的解释度分别为37.9%和30.7%;环境因子为影响SOC密度的主要因子.环境因子中.气温对SOC密度的影响大干降雨,其中气温和降雨的变化分别主要由海拔和纬度的变化引起的.除气温和降雨外,还有其它随海拔或经纬度而变化的因子也对SOC密度产生显著影响,这种影响要大于降雨的影响. 相似文献