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941.
A directional passive air sampler for monitoring polycyclic aromatic hydrocarbons (PAHs) in air mass
Tao S Liu YN Lang C Wang WT Yuan HS Zhang DY Qiu WX Liu JM Liu ZG Liu SZ Yi R Ji M Liu XX 《Environmental pollution (Barking, Essex : 1987)》2008,156(2):435-441
A passive air sampler was developed for collecting polycyclic aromatic hydrocarbons (PAHs) in air mass from various directions. The airflow velocity within the sampler was assessed for its responses to ambient wind speed and direction. The sampler was examined for trapped particles, evaluated quantitatively for influence of airflow velocity and temperature on PAH uptake, examined for PAH uptake kinetics, calibrated against active sampling, and finally tested in the field. The airflow volume passing the sampler was linearly proportional to ambient wind speed and sensitive to wind direction. The uptake rate for an individual PAH was a function of airflow velocity, temperature and the octanol-air partitioning coefficient of the PAH. For all PAHs with more than two rings, the passive sampler operated in a linear uptake phase for three weeks. Different PAH concentrations were obtained in air masses from different directions in the field test. 相似文献
942.
Potentially toxic metal contamination of urban soils and roadside dust in Shanghai, China 总被引:13,自引:0,他引:13
Shi G Chen Z Xu S Zhang J Wang L Bi C Teng J 《Environmental pollution (Barking, Essex : 1987)》2008,156(2):251-260
A detailed investigation was conducted to understand the contamination characteristics of a selected set of potentially toxic metals in Shanghai. The amount of Pb, Zn, Cu, Cr, Cd and Ni were determined from 273 soil/dust samples collected within urban area. The results indicated that concentration of all metals except Ni in soils was significant, and metal pollution was even severer in roadside dust. A series of metal spatial distribution maps were created through geostatistical analysis, and the pollution hotspots tended to associate with city core area, major road junctions, and the regions close to industrial zones. In attempt of identifying the source of metals through geostatistical and multivariate statistical analyses, it was concluded as follows: Pb, Zn and Cu mainly originated from traffic contaminants; soil Ni was associated with natural concentration; Cd largely came from point-sourced industrial pollution; and Cr, Ni in dust were mainly related to atmospheric deposition. 相似文献
943.
Yen JH Tsai PW Chen WC Wang YS 《Journal of environmental science and health. Part. B》2008,43(5):382-389
The fate of herbicides trifluralin, pendimethalin, alachlor and metolachlor in paddy field soils amended with plant materials was investigated. The plant materials were purple sesbania, vegetable soybean and rice straw. The investigation was performed at two temperatures (25 and 40 degrees C) and two soil water moistures (60 and 90% water-holding capacity). The results showed linear and Freudlich equations described the adsorption of amide compound to soil. Adsorption coefficient (K(d)) fit to linear equation were in general greater in plant material-amended soils than in non-amended soil, especially in soil amending with rice straw. Increasing temperature and soil water moisture content shortened the half-lives of compounds in various treated soils. The movement of compounds in the soil columns showed the maximum distribution of aniline type compound, trifluralin and pendimethalin, appeared at the upper top of 0 to 5 and 0 to 10 cm of soil column, respectively, and of anilide type, alachlor and metolachlor, were distributed at 0 to 25 cm of the soil column. The mobility of chemicals in the different treated soils was simulated by the behavior assessment model (BAM). There was no significant difference among different plant material incubated soils on dissipation and mobility of compounds in soils. 相似文献
944.
硝基修饰的超高交联树脂对酚类化合物的吸附研究 总被引:1,自引:0,他引:1
对超高交联聚苯乙烯树脂进行硝基修饰,制得硝基修饰超高交联聚苯乙烯树脂JN-5(简称JN-5).JN-5树脂具有比表面积高、亲水性强等优点.对酚类化合物在水溶液中进行静态吸附研究,平衡吸附试验数据和吸附热力学计算结果都表明,JN-5对4种酚类化合物(对甲基苯酚、苯酚、对氯苯酚、对硝基苯酚)的吸附性能优于大孔吸附树脂XAD-4.这主要得益于JN-5的高比表面积和丰富的微孔结构.动态小柱吸附试验中,在流速4.77mL/h、303K的条件下,JN-5对苯酚的穿透吸附量为2.43mmol/g,总吸附量为3.26mmol/g,吸附后的树脂能用8%(质量分数)的NaOH溶液完全洗脱. 相似文献
945.
序批式反应器生物强化处理苯酚废水的研究 总被引:1,自引:0,他引:1
将4株高效苯酚分解菌湿菌体分3批投加于序批式反应器(SBR),对活性污泥进行生物强化试验,分析活性污泥状态与性能变化,测定生物强化后对苯酚的降解能力.结果表明,随着生物强化过程的进行,沉降性能改善,污泥颗粒化趋势明显;生物强化后,活性污泥对苯酚降解能力、降解速率及对苯酚的耐受性明显提高:苯酚质量浓度为730~960mg/L时,苯酚完全降解时间可由正常的6h缩短至2h;6h内可完全降解苯酚的质量浓度由原来的880mg/L提高到2080mg/L,处理能力提高了1.36倍;当进水苯酚质量浓度增加到2400mg/L时,6h内污泥对苯酚的降解率仍达到60.1%. 相似文献
946.
947.
计算机模拟研究UO2+2在人体细胞液的形态分布 总被引:1,自引:0,他引:1
建立了由多种金属离子和小分子配体组成的多相细胞液热力学平衡模型.模拟研究了UO2 2在组织液和细胞液的形态分布及CO2-3、氨三乙酸(NTA)和乙二胺四乙酸(EDTA)浓度对细胞液中UO2 2形态分布的影响.在组织液中,正常生理pH下,当各形态UO2 2总摩尔浓度 [U]= 1.0×10-6 mol/L 或[U]=1.0×10-3 mol/L时,UO2 2均主要以[UO2(CO3)3]4-和[UO2(CO3)2]2-形态存在.在细胞液中,当[U]=1.0×10-6 mol/L时,UO2 2主要以[UO2(CO3)3]4-和[UO2(CO3)2]2-存在;当[U]=1.0×10-3 mol/L,pH为6.0~6.8时,细胞液中存在大量的固相(UO2)3(PO4)2·4H2O,当pH为6.8~7.4时,UO2 2主要以[UO2(CO3)3]4-、[UO2(CO3)2]2-和[(UO2)2CO3(OH)3]-存在.细胞液中(UO2)3(PO4)2·4H2O含量随[U]升高而增加.通过调节细胞液pH和增加细胞液CO2-3浓度均能降低其固相UO2 2配合物含量.在细胞液中增加NTA会增加(UO2)3(PO4)2·4H2O含量,当添加EDTA时会显著降低(UO2)3(PO4)2·4H2O含量. 相似文献
948.
949.
950.