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201.
含铀废水中铀的回收主要是基于材料与[UO2(H2O)5]2+中UO2(2+)之间的络合,但H2O的电偶极矩对络合有显著弱化作用。采用酰胺基两性分子N,N-二甲基-9-癸烯酰胺(NADA)氢键作用与[UO2(H2O)5]2+形成UO2[(H2O)x C12H23NO]n*(x<5,UO2-Coordination Compound,简称UO2-CC),选取惰性物质WS2为吸附材料,通过静态吸附试验(不同pH、接触时间、浓度和温度)分别研究其对UO22+和UO2-CC的吸附量。动力学拟合结果表明,二者的吸附反应是化学吸附过程,UO<  相似文献   
202.
Chelant-enhanced phytoextraction is one of the most promising technologies to remove heavy metals from soil. The key of the technology is to choose suitable additives in combination with a suitable plant. In the present study, laboratory batch experiment of metal solubilization, cress seeds germination were undertaken to investigate the metal-mobilizing capability and the phytotoxicity of organic additives, including ethylene diamine triacetic acid (EDTA), citric acid, acetic acid, oxalic acid, glutamine and monosodium glutamate waste liquid (MGWL) from food industry. Experiments in pots were carried out to study the effects of the additives on Zn and Cd phytoextraction. Furthermore, a leaching experiment with lysimeter was performed to evaluate the environmental risks of additive-induced leaching to underground water. The results showed that EDTA had a strong mobilizing ability for Zn and Cd, followed by mixed reagent (MR) and MGWL. MGWL and acetic acid at 5 mmol equivalent per liter resulted in seed germination index less than 2%. Experiments in pots verified the phytotoxicity of acetic acid and MGWL. Addition of the mixed reagent at 6--10 mmol/kg significantly increased Zn phytoextraction by Thlaspi caerulescens. The same for EDTA and the mixed reagent at 10 mmol/kg by Sedum dfredii. But only mixed reagents could significantly increase Cd phytoextraction by the studied hyperaccumulators. This suggested that the strong chelant was not always the good agent to enhance phytoextraction. S. alfredii combined with 2--10 mmol/kg soil MR was preferred for phytoremediation of Cd/Zn contaminated soils in southern China, this could result in high phytoextraction of Cd/Zn and reduce the leaching risk to underground water than EDTA assisted phytoextration.  相似文献   
203.
A mass transport model was developed to predict the transport rate of ions within biofilms, which was experimentally verified using the fluxes of NH4^+ and Ca^2+ through the heterotrophic biofilms with the thickness varying from 230 to 1430μm under the effect of external field in the range of-20 V/m to 60 V/m. It is found that the result predicted by the model is in agreement with the experimentally obtained one, with the error less than 5 percent for the thin biofilms. The error increases with the increase of the biofilm thickness. The transport rate of ions caused by electric migration is affected by the charges, field strength, and biofilm thickness and so on.  相似文献   
204.
In order to investigate the adsorption mechanism of trace metals to surficial sediments (SSs), a selective extraction procedure was improved in the present work. The selective extraction procedure has been proved to selectively remove and separate Fe, Mn oxides and organic materials (OMs) in the non-residual fraction from the SSs collected in Songhua River, China. After screening different kinds of conventional extractants of Fe and Mn oxides and OMs used for separation of heavy metals in the soils and sediments, NH2OH .HCl (0.1 mol/L) + HNO3 (0.1 mol/L), (NH4)2C2O4 (0.2 mol/L) + H2C2O4 (pH 3.0), and 30% of H2O2 were respectively applied to selectively extract Mn oxides, Fe/Mn oxides and OMs. After the extraction treatments, the target components were removed with extraction efficiencies between 86.09%--3.36% for the hydroxylamine hydrochloride treatment, 80.63%- 101.09% for the oxalate solution extraction, and 94.76%-102.83% for the hydrogen peroxide digestion, respectively. The results indicate that this selective extraction technology was effective for the extraction and separation ofFe, Mn oxides and OMs in the SSs, and important for further mechanism study of trace metal adsorption onto SSs.  相似文献   
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给水管壁生物膜会吸附水中的重金属元素积累在管壁生物膜中,在受到扰动时释放回到水体,危害饮用水水质安全。试验以上海管网末梢水为实验对象,研究了PVC、铸铁和紫铜等三种管材上生物膜对铅、镉的解吸特性。结果表明,PVC、铸铁和紫铜附着生物膜对铅的解吸容量qe分别为:5.92211μmol·m^-2、128.3051μmol·m^-2和21.1808,解吸速率常数k分别为:0.001060 m^2·μmol^-1·min^-1、0.000041 m^2·μmol^-1·min^-1和0.000503 m^2·μmol^-1·min^-1,对于镉元素三种材质的解吸容量qe分别为:14.71519μmol·m^-2、18.50481μmol·m^-2和2.25225μmol·m^-2;解吸速率常数k分别为:0.000102 m^2·μmol^-1·min^-1、0.001070 m^2·μmol^-1·min^-1和0.000103 m^2·μmol^-1·min^-1。  相似文献   
207.
208.
新疆吉木乃诸河水体氢氧同位素和水化学特征   总被引:2,自引:0,他引:2  
利用2018年6月和11月在新疆吉木乃诸河流域采集的河水、冰雪融水和降水样品,对流域水体的水化学成分和氢氧稳定同位素(D,~(18)O)组成的时间和空间特征进行了系统研究.结果表明,吉木乃诸河在丰水期和枯水期阳离子均以Ca~(2+)为主,阴离子以HCO~-_3为主,其次分别为Na~+和SO_4~(2-).在空间上,Na~+、Mg~(2+)、SO_4~(2-)、Cl~-随着海拔的降低呈增加趋势.通过Piper图可以判断出,吉木乃诸河水化学类型为HCO_3-Ca型.利用Gibbs图可知流域内主要离子组成与各类岩石的风化作用有关,大气降水和蒸发作用的影响相对较小.结合当地的水文地质情况,运用离子含量比值法,可以发现离子主要来源于流域内碳酸盐风化和含硫矿物的氧化.丰水期吉木乃诸河地表水中δ~(18)O和δD较枯水期高,冰川融水的同位素值没有明显的季节变化,降水中的同位素值季节变化较大,其区域大气降水线方程为δD=7.5δ~(18)O+5.4 (R~2=0.99).吉木乃诸河河水中稳定同位素与海拔呈现正相关关系,主要原因是蒸发作用的增加,地表水同位素值偏负.该区域地表径流与冰川融水密切相关,冰川融水对该流域水资源的补给贡献较大.  相似文献   
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