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Feng Qin Shujuan Wang Inna Kim Hallvard F. Svendsen Changhe Chen 《International Journal of Greenhouse Gas Control》2011,5(3):405-412
A reaction calorimeter was used to determine the enthalpies of absorption of CO2 in aqueous ammonia and in aqueous solutions of ammonium carbonate at temperatures of 35–80 °C. The heat of absorption of CO2 with 2.5 wt% aqueous ammonia solution was found to be about 70 kJ/mol CO2, which is lower than that with MEA (around 85 kJ/mol) at 35 and 40 °C. The value decreases with increased loading, but not to as low a value as expected by the carbonate–bicarbonate reaction (26.88 kJ/mol). The enthalpy of absorption of CO2 in aqueous ammonia at 60 and 80 °C decreases with loadings at first, then increases between 0.2 mol CO2/mol NH3 and 0.6 mol CO2/mol NH3, and then decreases again. The behavior of the heat of absorption of CO2 in 10 wt% ammonium carbonate solution was found to be the same as that of aqueous ammonia at loadings above 0.6 mol CO2/mol NH3. The heat of absorption increases with increasing temperature. The heats of absorption are directly related to the extent of the various reactions with CO2 and can be assessed from the species variation in the liquid phase. 相似文献
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Occurrence, distribution, and source of polybrominated diphenyl ethers in soil and leaves from Shenzhen Special Economic Zone, China 总被引:2,自引:0,他引:2
Pei-Heng Qin Hong-Gang Ni Yang-Sheng Liu Ye-Hong Shi Hui Zeng 《Environmental monitoring and assessment》2011,174(1-4):259-270
Polybrominated diphenyl ethers (PBDEs) were measured in soil and three plant species samples taken at different land use areas in Shenzhen China. The concentrations of ??7BDEs (BDE-28, BDE-47, BDE-99, BDE-100, BDE-153, BDE-154, and BDE-183) and BDE-209 in the surface soils ranged from 0.23 to 271 and 8.9 to 5,956 ng/g dry weight (dw), respectively. These figures are comparable to that in the soils of electronic waste dismantling sites. BDE-209 was the predominant congener (contributes 85?C99% of ??8PBDEs (??7PBDEs plus BDE-209)) in soils. The regression slopes of total organic carbon and individual BDE congeners were rather gentle, indicating that factors other than soil organic matter regulated the soil concentrations. Proximity to sources of deposition processes might be the major factors. In the plant leaves, ??7BDEs and BDE-209 concentrations ranged from 1.29 to 5.91 and 5.49 to 28.2 ng/g dw, respectively. BDE-209 is also the dominant component, but the contribution was much lower compared with that in soils. Bauhinia purpurea Linn. and Michelia alba DC. show some similarities on the uptake of PBDEs, while Ficus microcarpa var. pusillifolia is different from them. The correlations between plant leaf concentrations and predicted gaseous concentrations were moderate, indicating that gaseous concentration did not influence the leaf concentration significantly. 相似文献
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对臭氧氧化去除饮用水中微囊藻毒素RR及LR的降解效能、反应动力学进行了试验研究,讨论了藻毒素初始质量浓度、pH值、羟基自由基(·OH)抑制剂(HCO-3)、溶解性有机碳(DOC)质量浓度对降解的影响.结果表明:整个降解过程符合一级动力学反应方程,降解速率常数与藻毒素初始质量浓度无关;pH值的升高、HCO-3和DOC的存在都会降低藻毒素的降解效率.在液相臭氧质量浓度为8.20 mg·L-1,pH=7.0,温度为(25±1) ℃,反应时间30 min的条件下,MC-RR降解速率常数k=7.80×102 min-1,去除率达90.0%;MC-LR降解速率常数k=1.06×101 min-1,去除率达96.3%. 相似文献
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Our previous study indicated that the current level of polycyclic aromatic hydrocarbons (PAHs) in Shenzhen soil is in the low-end of world soil PAH pollution. In this study, the fate of PAHs in the soil of Shenzhen was investigated. The mass inventories of Σ(27)PAHs and Σ(15)PAHs (defined as the sum of the 27 or 15 PAH compounds sought) in topsoil of Shenzhen were ~204 and ~152 metric tons, respectively. Fate estimation of Σ(15)PAHs shows that air-soil gaseous exchange is the primary environmental process with ~10,076 kg/year diffusing from soil to air. Rain washing (~1131 kg/year from air to soil) is the most important input pathway followed by wet (~17 kg/year) and dry deposition (~8 kg/year) to soils in Shenzhen. The transport of Σ(15)PAHs by soil erosion is a crucial loss process for soil PAHs in Shenzhen (1918 kg/year for water runoff and 657 kg/year for solid runoff from soil). Moreover, degradation is not ignorable at present (95 kg/year). Comparison of inventory and residue (defined as Σ(15)PAHs left in topsoils after all environmental loss processes) suggested that input and loss of high molecular weight PAHs for Shenzhen's soil reached apparent equilibrium. Soil PAH pollution in Shenzhen will stay in a quasi-steady state for a long period and the natural environmental processes can not significantly reduce the pollution. 相似文献
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通过采集海拉尔盆地地表水样品12件,地下水样品67件,运用Durov图、等值线图和铀形态计算理论,结合数理统计方法,分析研究区域地下水铀的分布特征和赋存形态,结果表明:海拉尔盆地赫尔洪德凹陷地区主要为HCO3-Ca·Na型,蹉岗隆起、乌尔逊凹陷和贝尔凹陷地区主要为Cl-Na型和HCO3-Na型,巴彦山隆起地区主要为HCO3-Na型,红旗牧场和新宝力格凹陷主要为Cl-Na型.研究区域铀的分布范围为17~425μg/L,平均值为80μg/L,标准偏差为70μg/L,引发了区域地源性地下水铀污染问题.地下水中以UO2(CO3)34-和UO2(CO3)22-的主要形式存在,与Eh表现的氧化还原环境具有一致性,其中呼伦贝尔湖东南部属于地下水铀成矿有利区域.潜在铀成矿范围属于重碳酸铀酰占优势的HCO3型含铀地下水,铀酰碳酸盐复合物应占主导地位,铀的溶解与HCO3-的增加有关,地下水中的铀存在参与碳酸盐岩和硫酸盐岩的混合溶滤作用的可能性,UO2(CO3)34-、UO2(CO3)22-、U4O9和沥青铀矿等处于饱和状态,总Fe和(Ca2++Mg2+)浓度较低,各种水化学指标对铀富集具有指示意义,因此可将其视为潜在铀源的参考依据. 相似文献
300.
为了解四川盆地大气中单颗粒气溶胶理化特征,分别在该区域典型城市(成都市)和背景地区(峨眉山)进行了大气单颗粒样品采集.基于带能谱的透射电子显微镜(TEM-EDS)对两地累计3923个单颗粒的化学组成、形貌特征及混合状态等进行了全面观测和分析,并对两地颗粒物差异性进行了对比分析.结果发现:两地气溶胶颗粒主要包括有机物、富硫、矿物、烟尘和飞灰/金属颗粒,除了以单独的外混形式存在外,大多数颗粒以两种及两种以上颗粒类型混合(即内混)形式存在.通过对成都市不同污染状况下单颗粒特征对比发现,"污染天"的内混颗粒占比高于"清洁天",分别为74.2%和68.6%;相比"清洁天","污染天"颗粒物粒径分布范围更广且峰值区间更大,表明污染过程中颗粒物的大气混合趋于更强.对比成都市与峨眉山分析结果得知,成都市以内混的有机物-硫颗粒为主导(占比为50.2%),而峨眉山以外混的有机物颗粒为主导(占比为50.5%);成都市含硫类颗粒物(如有机物-硫颗粒)贡献高于峨眉山,而峨眉山两种含碳类颗粒(如烟尘和有机物-烟尘颗粒)占比高于成都市;此外,成都市与峨眉山两地大气颗粒物粒径分布范围及峰值区间均存在一定差异,进一步体现了两地颗粒物来源和老化混合的差异.在峨眉山,与非降雨天相比,一些易溶于水的颗粒物(如含硫类颗粒)在降雨天占比明显降低,而源自当地燃烧过程、粒径较小且疏水性强的颗粒物(如烟尘和有机物-烟尘颗粒)占比相应升高. 相似文献