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761.
Total organic carbon, humic substances, and the species of trace metals (including Cu, Zn, Pb, Cd, Cr, Mn and Fe) in six and seven phases, such as bioexchangeable (P1), skeletal (carbonates, P2), easily reducible (Fe and Mn oxides, P3), moderately reducible (crystalline Mn oxides, P4), organic matters with sulphides (P5), and detritus with minerals (P6) as well as organic with humic substances (PB4) and organic residues (PB6), were analyzed in sediments from the Taiwan Erhjin coastal (including river and estuarine) area, where places we found the copper pollution. Results indicate that higher percentages of P1 and P2 for copper, zinc, lead, cadmium and manganese in samples collected in March and September of 1990 were much higher than those in P3-P6. High percentages of chromium and iron in samples respectively collected in March and September of 1990 were found in P6. for the seven phase analysis, higher percentages of copper species in PB4 and PB6 as well as iron species in PB7 were observed. On the other hand, purified humic acid with the high contents of manganese and iron in humic acid as well as purified fulvic acids were generally found at the upstream stations; and low values at coastal stations. However, extremely high copper (as high as 1750μg g-1, dry weight in fulvic acid and 820μg g-1 in humic acid) and lead (821μg g-1 in humic acid) concentrations with relatively high manganese and iron concentrations were observed in humic substances from the station near the copper recycling area. Comparing the results obtained from the Antarctic Ocean sediments with those from the Taiwan Erhjin Chi coastal sediments, the human impacts on the latter are evaluated.  相似文献   
762.
Cathode ray tube (CRT) glass is considered a hazardous material due to its lead toxicity. In addition, current disposal practices are being phased out due to their adverse environmental impacts. In this project, CRT glass was used as a fine aggregate replacement in concrete. Life-cycle material characterization was conducted by evaluating the durability and strength of the CRT-Concrete. Leaching tests were also conducted to investigate whether the material meets drinking water limits for Pb. Test results show that the plastic state of the CRT-Concrete was affected by the angularity of the glass particles. Moreover, the compressive strength of CRT-Concrete met and exceeded that of the control specimen. However, CRT-Concrete was susceptible to expansive alkali-silica reactions when more than 10% CRT replacement was used. Environmental leaching results show that lead concentrations from CRT-Concrete are below the drinking water limits depending on the CRT volume replacement and if biopolymers are used.  相似文献   
763.
This study investigates the distributions and enrichments of trace metals in suspended and sinking particulate matter from southern East China Sea (ECS) north of Taiwan during the period April 1992 to April 1993. According to these results, concentration of suspended particulate matter in the inner shelf of southern China Sea, the upwellinginfluenced shelf break, and in Kuroshio water are 1.30 (surface)-4.2 (bottom) mg1-1, ca. 0.4 mg1-1 and 0.1-0.2 mg1-1, respectively, reflecting various influences of terrestrial inputs. A benthic nepheloid layer (BNL), apparently owing to resuspension of local and/or remote bottom sediments, formed over the shelf region. Temporal variations in trace metal contents and enrichments in suspended matter from the shelf region reflect the variation of metal inputs from Chinese rivers, particularly from the Changjiang runoff. the enriched metals are more likely to be derived from anthropogenic input, rather than from biological accumulation. in addition, a decrease in metal contents and an increase in salinity confirm the transport of suspended particulate metals from the East China Sea shelf to the open ocean. the feature of metal plume in the intermediate layer (550-800m) of Kuroshio water also verifies this occurrence. Moreover, the sinking particles collected from a sediment trap on the upper slope are relatively enriched in lithogenic matter and trace metals, suggesting the deposit of anthropogenic metals in the slope area.  相似文献   
764.
Application of Amberlite XAD-7 impregnated with morpholine dithiocarbamate (MDTC) for separation and preconcentration of trace amounts of lead, copper, cobalt, iron, nickel, cadmium and zinc and determination by ICP-AES has been described. The optimum experimental parameters, such as pH, sample flow rate, eluent and effect of matrix ions on the preconcentration were investigated. Simultaneous enrichment of the seven metals was accomplished. The t 1/2 values for sorption are 2.9, 3.3, 3.7, 3.6, 2.8, 4.1 and 2.8 respectively for Pb(II), Cu(II), Co(II), Fe(III), Ni(II), Cd(II) and Zn(II). The method was applied for the determination of trace metal ions in seawater and natural water samples. The results have been compared with extraction GFAAS method.  相似文献   
765.
The carpophores of Parasol Mushroom and underlying soil substrate collected from several unpolluted and spatially distant sites across Poland were examined to know content and bioconcentration potential of mercury by this species. The total mercury content of the caps of Parasol Mushroom for the particular sites ranged from 1.1 ± 1.0 to 8.4 ± 7.4 μ g/g dry matter (total range from 0.05 to 22 μ g/g dm), while in the stalks were from 0.53 ± 0.27 to 6.8 ± 7.1 μ g/g dm (total range from 0.078 to 20 μ g/g dm). A top soil layer (0–10 cm) showed baseline mercury concentration from 0.022 ± 0.011 to 0.36 ± 0.16 μ g/g dm (total range from 0.010 to 0.54 μg/g dm). Parasol Mushroom is an effective mercury accumulator in the carpophores and bioconcentration factor (BCF) values of this element in the caps and depending on the sampling site ranged from 16 ± 6 to 220 ± 110 (total range from 0.52 to 470), while for the stalks were from 7.6 ± 2.6 to 130 ± 96 (total range from 0.52 to 340). It seems reasonable to state that tolerance (maximum allowable concentration) of the total mercury in a single cap of Parasol Mushroom at unpolluted areas should not exceed 25 μ g/g dm. A value greater then 25 μ g/g dm will imply an elevated content due to site pollution problems. Nevertheless, knowledge on highly toxic methylmercury content and its fraction in the total mercury content of Parasol Mushroom is lacking.  相似文献   
766.
东江流域水环境中颗粒态和胶体态金属元素的分布和来源   总被引:2,自引:0,他引:2  
运用连续流离心机和切面流超滤分离技术,从东江流域的水库、河流、河口3种水体中分离了大量的悬浮颗粒物(0.45μm)和胶体(1 nm~0.45μm),并用元素分析仪和电感耦合等离子体/质谱(ICP-MS)对有机碳和金属进行了表征.通过对比3种水体中颗粒态金属的含量(μg·g-1)和浓度(ng·L-1)发现,水库颗粒物有更高的重金属含量,与其在有机碳上的富集有关;河流颗粒物有更高的金属浓度,与地表径流和人为排放有关.另外,随着有机质含量的增加,湖泊水体中多种重金属的含量呈现先增加后降低的关系,显示了生物富集和生物稀释的双重作用.从东江中游到河口样品,Mg、Ti、Co、Ni等元素在颗粒物中的含量依次升高,Cu、As、Cd、Sn、Sb等元素则依次降低,这与海水的稀释作用以及与盐度变化引起的絮凝沉降有关.河流中胶体态金属的含量与浓度均大于水库,显示了河流受到更多的人类活动影响.虽然重金属主要分布在颗粒物中,但对比各种重金属的含量在颗粒态和胶体态中的顺序变化,发现地表径流带来的地壳元素倾向于分布在颗粒态中,而人为排放来源的金属倾向于分布在胶体态中.  相似文献   
767.
超临界水气化处理对脱水污泥中重金属环境风险的影响   总被引:1,自引:0,他引:1  
马倩  朱伟  龚淼  张会文  徐骏 《环境科学学报》2015,35(5):1417-1425
为探究超临界水气化前后脱水污泥中重金属的变化及生态风险,从重金属(Ni、Cu、Zn、Pb、Cr)的含量、化学形态分布及浸出毒性等多方面出发,利用地层累积指数(Igeo)、潜在生态风险指数(RI)和风险评估指数法(RAC)对江苏地区10种不同种脱水污泥超临界水气化前后重金属的环境生态风险进行综合评价.结果表明:不同污水厂脱水污泥经超临界水气化处理后,绝大部分污泥中重金属浸出毒性和生物可利用组分重金属含量明显降低,即处理后重金属的直接环境风险大大降低.不同重金属含量的脱水污泥经超临界水气化处理后,重金属环境污染程度及潜在生态风险程度显著降低,环境风险值被降至相对安全水平,对环境表现出低风险或无风险.p H值在一定程度上影响处理后污泥中重金属的环境风险.超临界处理时,污泥的p H呈现酸性时会引起反应釜腐蚀,从而导致固相残渣中Ni、Cr的生物可利用组分含量增加,当p H呈现碱性时则更利于重金属以稳定形态富集到固相产物中.  相似文献   
768.
杭州市河道底泥重金属污染评价与环保疏浚深度研究   总被引:5,自引:0,他引:5  
重金属是河道底泥疏浚要控制的重要污染物,而疏浚深度是生态疏浚工程中需要确定的关键参数.本文以杭州经济技术开发区河道为研究对象,共采集18处底泥柱状样,采用土壤背景值、土壤环境质量二级标准值、变异系数和相关性分析方法对底泥中Cu、Zn、Pb、Cd、Ni、As的污染状况进行了评价,同时分析重金属总量和有效态含量在垂向上的变化特征,并引入地累积指数法对各深度底泥中的重金属进行累积性评估,利用本文提出的临界累积深度方法来确定合理的环保疏浚深度.结果表明,河道表层底泥中Cu、Zn、Pb、Cd、Ni、As的平均含量分别为165.16、342.40、55.34、3.61、34.06、36.70 mg·kg-1,Cd、Cu、As、Zn的有效态含量分别为0.007、3.37、0.095、20.76 mg·kg-1,重金属总量均超过了杭嘉湖平原土壤背景值,其中Cd污染最为严重.各重金属元素在底泥中的变异系数为0.29~2.39,空间分布并不均匀.重金属总量和有效态含量随底泥深度的增大整体呈下降趋势,但受不同时期人类活动污染及河道整治影响而呈不规则变化.各重金属元素的富集程度为CdAsZnPbNiCu,其中,Cd污染等级为2~6级,污染程度为中度污染至极强污染.利用临界累积深度方法推算得到研究区域河道底泥环保疏浚深度为0~0.9 m.  相似文献   
769.
南四湖南阳湖区河口与湖心沉积物重金属形态对比研究   总被引:4,自引:0,他引:4  
湖泊河口区与湖心区沉积条件不同,沉积物重金属等内源污染物的分布亦可能存在较大区别.为比较河口区与湖心区沉积物重金属赋存形态的空间差异,利用柱状沉积物采样器在南四湖南阳湖区湖心和河口分别获取原位柱状沉积物,在比较分析沉积物孔隙度、有机质、粒度及典型重金属(Cu、Pb、Cd、Cr、Hg)各形态垂向分布特征的基础上,对其相关性进行分析,并对表层(0~4 cm)沉积物重金属污染程度及潜在生态风险进行评价.结果表明,除Cd外,河口区沉积物Cu、Pb、Cr、Hg含量较湖心区高,泗河为南阳湖区重金属污染物的来源之一,沉积物重金属各形态含量在垂向分布上规律性不明显,且均主要以残渣晶格结合态存在,5种重金属元素中,Hg残渣晶格结合态所占比重最小(约30%),具有较高的迁移性,存在相对较大的生态风险.地积累指数法和潜在生态危害指数法研究结果表明,河口区与湖心区表层沉积物均受Hg及Cd的污染较重,Pb、Cu、Cr污染较轻,潜在生态危害指数法所得污染级别较地积累指数法高.相关性分析表明,沉积物Cu、Pb、Cd、Cr、Hg总量、可交换态、有机物及硫化物结合态、残渣晶格结合态含量与沉积物孔隙度、有机质相关系数多为正值,同粒度相关系数多为负值,同碳酸盐结合态和铁锰氧化物结合态的相关系数各异,无明显规律.  相似文献   
770.
重金属污染物随工业废水排放到环境中,并通过生物链的富集作用,对环境和人类健康造成极大危害.自然界中很多微生物对重金属具有吸附性、耐受性和减小毒性损伤的特点.其中,细菌因其结构简单且易于培养,被广泛应用于研究对重金属的抗性及解毒.选取银(Ag)、铜(Cu)、铅(Pb)和铬(Cr)4种重金属,结合国内外的研究成果,系统地探讨了细菌对重金属的抗性及解毒机理.  相似文献   
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