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851.
K. M. S. Sundaram S. Y. Szeto 《Journal of environmental science and health. Part. B》2013,48(5):579-599
Abstract An oil‐based formulation of carbaryl (1‐naphthyl N‐methyl‐carbamate) (Sevin‐2‐Oil) was applied twice by a fixed‐wing aircraft at a dosage rate of 280 g of A.I./ha/application to a coniferous forest near Allardville, New Brunswick. The highest concentrations of the chemical in fir foliage, litter and forest soil 1 h after application were respectively 4.20, 1.21 and 0.59 ppm (fresh weight). The residues dissipated rapidly and the DT50 values obtained from the depletion curves were 2.3 d for foliage and 1.5 d for litter and soil samples. Very low levels (<0.1 ppm) of carbaryl persisted in foliage and litter beyond the 10 d sampling period. The maximum residue level found in stream water was 0.314 ppm and more than 50% of it had dissipated within 1 h. Low but detectable levels (0.001 ppm) of the chemical persisted in water until the end of the 10 d sampling period. Sediment samples contained a maximum level of 0.04 ppm, which dissipated below the detection limit within 5 h. Brook trout and slimy sculpins captured in the stream 1 d after the spray contained on average about 0.04 ppm of carbaryl and none of it was found in 3 d postspray samples. 相似文献
852.
853.
K.M.S. Sundaram A. Sundaram 《Journal of environmental science and health. Part. B》2013,48(4):757-783
Abstract Dimilin® WP‐25, a wettable powder formulation of diflubenzuron (DFB) [1‐(4‐chlorophenyl)‐3‐(2,6‐difluorobenzoyl) urea], was formulated in four different carrier liquids, viz., water; a light petroleum paraffinic oil, ID 585; a heavy paraffinic oil, Sunspray® 7N; and a 1:2 mixture of a light petroleum aromatic solvent (Cyclosol® 63) and canola oil; to provide four end‐use mixtures, Dim‐W, Dim‐585, Dim‐7N and Dim‐Cy‐C respectively, each containing 28 g of DFB per litre. Balsam fir branch tips clipped from greenhouse‐grown seedlings, and sugar maple branch tips clipped from field‐grown young trees, were exposed to uniform‐sized droplets (ranging in diameters from 135 to 190 μm) of the four end‐use mixtures which were atomized using a monodispersed droplet generator. Droplets were collected on the fir and maple branch tips and the initial residue per g fresh weight of foliage was determined by high‐performance liquid chromatography (HPLC). The branch tips were exposed to cumulative rainfall of 3, 6 and 10 mm at an intensity of 5 mm/h and at time intervals of 1, 12, 36 and 72 h after DFB treatment, to test the influence of ‘ageing’ of foliar residues on rainfastness. Foliar samples were collected for residue determination just before the onset of rainfall, and at 0.5 h post‐rain. DFB was quantified by the HPLC method. In the case of fir foliage, the Dim‐W formulation was the most susceptible to rain‐washing and the rainfastness did not increase with the ageing period of foliar deposits. In contrast, the three oil‐based mixtures showed greater rainfastness depending upon the carrier liquid and the ageing period. Rainfastness decreased in the order of Dim‐Cy‐C > Dim‐7N > Dim‐585 > Dim‐W. In contrast, the data on maple foliage indicated that the ageing of deposits increased the rainfastness of all the 4 end‐use mixtures. Dim‐585 was the most susceptible to rain washing, and rainfastness decreased in the order of Dim‐W > Dim‐Cy‐C > Dim‐7N > Dim‐585. 相似文献
854.
Suresh Maddila Surjakanta Rana Ramakanth Pagadala Surya N. Maddila Chandrasekhar Vasam 《Journal of environmental science and health. Part. B》2013,48(8):571-583
Triclopyr is a widely used pesticide which is non-biodegradable and enters aquatic systems. The ozone facilitated photocatalyzed degradation and mineralization of Triclopyr using Au-loaded titania as heterogeneous catalyst is reported. The oxidative degradation activity of the hazardous pesticide was investigated at pH 7.8 under varied reaction conditions, including in presence and absence of ozone, titania alone, in presence and absence of light and with different loadings of Au on support. Photocatalysis with 2% Au/TiO2 in the presence of ozone yielded 100% degradation of Triclopyr in 2 h. The extent of degradation of pesticide and its mineralization were confirmed by GC-MS. For 10 mg/L of Triclopyr, 0.1 g/L of catalyst was found to be the optimum for mineralization. Results show that photocatalyzed ozonation with Au/TiO2 as catalyst is a very effective for its removal. No leaching of Au was observed in triplicate runs. Catalyst was fully recoverable and reusable with no loss of activity. 相似文献
855.
856.
电解法处理含镍废水及纯镍的回收 总被引:1,自引:0,他引:1
雷英春 《城市环境与城市生态》2009,(3)
采用电解回收法处理Ni2+含量为2g/L的废水,在阴极回收纯镍。研究了电解电流、极距、NH4Cl浓度、pH值等因素对Ni2+去除率、槽压、阴极能耗的影响,得出最优工艺参数为:温度20℃,电解时间20min时、电解电流300mA,极距15mm,NH4Cl浓度5g/L,pH值8.0,该条件下Ni2+去除率为96.926%,槽压16.21V,阴极能耗22.418kW.h/kg,在阴极可得到沉积6.45μm厚的镍板。 相似文献
857.
858.
Enrique J. La Motta 《Journal of the American Water Resources Association》1995,31(2):207-216
ABSTRACT: This paper presents a discussion of the chemistry of CO2 removal in tray aerators, and different sets of equations that are applicable to several initial water chemical conditions are proposed. These chemical equations and a statistical model to predict the kinetic constant were tested with field data observed by other researchers in pilot units and in a full scale plant. The water temperature in their experiments was around 15°C. 相似文献
859.
西南地区1959—1961年三年自然灾害分析 总被引:1,自引:1,他引:1
该文以丰富而翔实的资料就西南地区1959~1961年三年自然灾害,特别是旱灾的灾情、灾情特点、灾害损失、灾害原因及其经验教训进行了论述. 相似文献
860.
DSD酸氧化缩合废水浓缩液回用试验研究 总被引:4,自引:1,他引:4
研究了DSD酸氧化缩合废水浓缩液回用到原生产过程的可行性。对DSD酸氧化缩合废水可采用萃取技术分离出其中97%的有机物,反萃产生的4-8倍的浓缩液返回到DSD酸生产中的氧化缩合单元后,可提高DNS酸的收率约7.43%,且不会明显影响产品的纯度,浓缩液8次循环磁用试验的结果表明,虽然DSD酸氧化缩合废水的COD从15000-20000mg/L提高到20000-29000mg/L,但没有显著持续增长的趋势,表明反应液中副产物的浓度得到了有效的控制。 相似文献