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41.
Higher concentrations of Hg can be emitted from coal pyrolysis or gasification than from coal combustion, especially elemental Hg. Highly efficient Hg removal technology from coal-derived fuel gas is thus of great importance. Based on the very excellent Hg removal ability of Pd and the high adsorption abilities of activated carbon(AC) for H2 S and Hg, a series of Pd/AC sorbents was prepared by using pore volume impregnation, and their performance in capturing Hg and H2 S from coal-derived fuel gas was investigated using a laboratory-scale fixed-bed reactor. The effects of loading amount, reaction temperature and reaction atmosphere on Hg removal from coal-derived fuel gas were studied. The sorbents were characterized by N2 adsorption, X-ray diffraction(XRD) and X-ray photoelectron spectroscopy(XPS). The results indicated that the efficiency of Hg removal increased with the increasing of Pd loading amount, but the effective utilization rate of the active component Pd decreased significantly at the same time. High temperature had a negative influence on the Hg removal. The efficiency of Hg removal in the N2-H2S-H2-CO-Hg atmosphere(simulated coal gas) was higher than that in N2-H2S-Hg and N2-Hg atmospheres, which showed that H2 and CO, with their reducing capacity, could benefit promote the removal of Hg. The XPS results suggested that there were two different ways of capturing Hg over sorbents in N2-H2S-Hg and N2-Hg atmospheres. 相似文献
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春、夏季长江口及其邻近海域溶解N2O的分布和海-气交换通量 总被引:1,自引:1,他引:0
分别于2012年3月和7月对长江口及其邻近海域进行了调查,对水体中溶解氧化亚氮(N2O)的分布及海-气交换通量进行了研究.结果表明,春季长江口及其邻近海域表层海水中溶解N2O浓度范围为9.34~49.08 nmol·L-1,平均值为(13.27±6.40)nmol·L-1.夏季表层溶解N2O浓度范围为7.27~27.81 nmol·L-1、平均值为(10.62±5.03)nmol·L-1.两航次表、底层海水中溶解N2O浓度相差不大.长江口溶解N2O浓度由近岸向外海逐渐降低,受陆源输入影响显著.溶解N2O浓度高值出现在长江口最大浑浊带附近,这主要是由于水体中较高的硝化速率造成的.温度是影响N2O分布的另一个重要因素,对溶解N2O浓度有双重作用.春季和夏季表层海水中N2O饱和度范围分别为86.9%~351.3%和111.7%~396.0%,平均值分别为(111.5±41.4)%和(155.9±68.4)%,大部分站位处于过饱和状态.利用LM86、W92和RC01公式分别计算了长江口及其邻近海域N2O的海-气交换通量,春季分别为(3.2±10.9)、(5.5±19.3)和(12.2±52.3)μmol·(m2·d)-1,夏季分别为(7.3±12.4)、(12.7±20.4)和(20.4±35.9)μmol·(m2·d)-1,初步估算出长江口及其邻近海域的年平均释放量分别为0.6×10-2Tg·a-1(LM86)、1.1×10-2Tg·a-1(W92)、2.0×10-2Tg·a-1(RC01).长江口及其邻近海域虽然只占全球海洋总面积的0.02%,但其释放的N2O占全球海洋释放量的0.06%,表明长江口及其邻近海域是产生和释放N2O的活跃区域. 相似文献
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The potential of cost-effective coconut husk for the removal of toxic metal ions for environmental protection 总被引:2,自引:0,他引:2
Coconut (Cocos nucifera) husk, an agricultural waste, has been thoroughly investigated for the removal of toxic Cd(II), Cr(III) and Hg(II) ions from aqueous media. The parameters like nature and composition of electrolyte, concentration of toxic ions, dosage of coconut husk, and equilibration time between the two phases were optimized for their maximum accumulation onto the solid surface. The effect of common ions on the uptake of metal ions has been monitored under optimal conditions. The variation of retention of each metal ion with temperature was used to compute the thermodynamic quantities DeltaH, DeltaS and DeltaG. The values 18.1+/-0.6 kJmol(-1), 74+/-2 Jmol(-1)K(-1), and -3.8+/-0.04 kJmol(-1) at 298 K; 10.8+/-0.8 kJmol(-1), 48.8+/-2.7 Jmol(-1)K(-1), and -4.6+/-0.3 kJmol(-1) at 298 K; and -37.4+/-2k Jmol(-1), 105+/-7 Jmol(-1)K(-1) and -2.58+/-0.5 kJmol(-1) at 298 K were obtained for Cd(II), Cr(III) and Hg(II) ions, respectively. The sorption data were analysed by applying different sorption isotherms. The sorption capacity and energy were evaluated for each metal ion. The values of the Freundlich constants 1/n and C(m) were 0.92+/-0.04 and 52.6+/-22.2 mmolg(-1); 0.85+/-0.05 and 56.0+/-0.03 mmolg(-1); and 0.88+/-0.03 and 6.84+/-0.45 mmolg(-1) for Cd(II) Cr(III) and Hg(II) ions, respectively. Similarly, the Dubinin-Radushkevich (D-R) constants beta, X(m,) and E were evaluated for the three metal ions. To check the selectivity of the sorbent, sorption of a number of elements was measured under similar conditions. Separation of Zn(II) from Cd(II); Cr(III) from I(I), Zr(IV), Se(IV), and Hg(II) from Se(IV) and Zn(II) can be achieved using this sorbent. This cheap material has potential applications in analytical chemistry, water decontamination, industrial effluent treatment and in pollution abatement. 相似文献
47.
采用钙基吸收剂及复合氧化剂半干法脱除模拟球团烟气中的SO_2及Hg~0,考察了多因素条件对吸收效果的影响。实验结果表明,在以NaClO和NaClO_2为复合氧化剂、 NaClO与NaClO_2体积比1∶0.5、复合氧化剂质量分数3%、反应温度110℃、钙基吸收剂质量3.0 g、模拟烟气进气流量1.2 L/min的条件下,SO_2和Hg~0的脱除率分别为98%和93%,证明钙基吸收剂与复合氧化剂对污染物球团烟气中的SO_2和Hg~0有良好的脱除作用。 相似文献
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对碱激胶凝材料(碱-偏高岭土、碱-矿渣和碱-粉煤灰)与水-水泥体系固化Ph^2+进行了试验研究,其中水-水泥体系为对比样。结果表明:对于相同稠度的碱激发胶凝材料,即使Pb^2+含量达到2.4%,除了碱-粉煤灰的抗压强度略低外,其他都达到30MPa以上,满足填埋或做建筑基材的使用要求;与水泥相比,碱激发胶凝材料能显著降低重金属离子(Ph^2+)浸出浓度,其规律性与其NH4交换容量大小的规律性一致,与其固化体的抗压强度的大小没有相关性。 相似文献
50.
Soil and atmospheric concentrations, dry deposition and soil-air gas exchange of organochlorine pesticides (OCPs) were investigated at an industrial site in Aliaga, Izmir, Turkey. Current-use pesticides, endosulfan and chlorpyrifos, had the highest atmospheric levels in summer and winter. Summertime total (gas + particle) OCP concentrations in air were higher, probably due to increased volatilization at higher temperatures and seasonal local/regional applications of current-use pesticides. Particle deposition fluxes were generally higher in summer than in winter. Overall average dry particle deposition velocity for all the OCPs was 4.9 ± 4.1 cm s−1 (average ± SD). ΣDDXs (sum of p,p′-DDT, p,p′-DDD, and p,p′-DDE) were the most abundant OCPs in Aliaga soils (n = 48), probably due to their heavy historical use and persistence. Calculated fugacity ratios and average net gas fluxes across the soil-air interface indicated volatilization for α-CHL, γ-CHL, heptachlorepoxide, cis-nonachlor, trans-nonachlor, and p,p′-DDT in summer, and for α-CHL, γ-CHL, trans-nonachlor, endosulfan sulfate, and p,p′-DDT in winter. For the remaining OCPs, soil acted as a sink during both seasons. Comparison of the determined fluxes showed that dry particle, gas-phase, and wet deposition are significant OCP input mechanisms to the soil in the study area. 相似文献