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331.
采用连续流生物活性炭(BAC)工艺处理水中挥发性苯系物(BTEX,包括苯、甲苯、乙苯、二甲苯),评价进水负荷、活性炭炭型等因素对于BAC处理性能的影响.研究表明,在40d的处理时间内,除苯之外,其余BTEX的BAC出水中均未检出苯系物(进水为6mg/L).为了检验BAC在高BTEX负荷情况时的处理效果,将进水浓度设定为19~32mg/L左右,在EBCT为1.2min条件下同样只有苯的出水浓度上升至10mg/L(C/Cin为0.45),然后略有下降,最终保持在5~10mg/L(C/Cin为0.3以下),其余苯系物出水浓度均一直保持小于5mg/L.这表明BAC可以有效地处理高负荷BTEX(8.68~12.9kgTOC/(m3·d))的进水.生物活性炭对于活性炭吸附容量的恢复有比较明显的作用,煤质炭和椰壳炭的生物再生效率分别为53.6%和26.6%,煤质炭再生效率高的原因可能是其具备更多的大型中孔和大孔. 相似文献
332.
酸化液对厌氧释磷好氧吸磷速率的影响研究 总被引:3,自引:1,他引:2
采用序批式试验研究了酸化液对聚磷菌厌氧释磷好氧吸磷速率的影响。同一活性污泥混合液中聚磷菌的释磷潜力相当,混合液中挥发性脂肪酸越多则越有利于激发聚磷菌的释磷潜能。酸化液投加量越大,对应的混合液中聚磷菌的平均释磷速率也越大。当酸化液投加量为30 mg/L(以TOC计)时,聚磷菌的平均释磷速率达0.137 mg/(mg.d),是未投加酸化液工况的3.26倍。聚磷菌厌氧释磷过程中,活性污泥的MLVSS值逐渐增大,而MLSS值却不断减小,这是由聚磷菌释磷反应过程中聚磷颗粒和糖原的消耗,以及PHB的生成而产生的。碳源充足与否,对聚磷菌的平均好氧吸磷速率影响不大,研究各工况中,聚磷菌的平均吸磷速率在0.129~0.160 mg/(mg.d)内。碳源越充足,则聚磷菌在好氧吸磷反应持续的时间越长,因此,具有更强的超量吸磷能力。酸化液投加量为20 mg/L时(以TOC计),聚磷菌在好氧吸磷结束时,出水的SP浓度能减少到0.5 mg/L以下。 相似文献
333.
Removal of phosphate by Fe-coordinated amino-functionalized 3D mesoporous
silicates hybrid materials
Phosphate removal from aqueous waste streams is an important approach to control the eutrophication downstream bodies of water.
A Fe(III) coordinated amino-functionalized silicate adsorbent for phosphate adsorption was synthesized by a post-grafting and metal
cation incorporation process. The surface structure of the adsorbent was characterized by X-ray di raction, N2 adsoropion/desoprotion
technique, and Fourier transform infrared spectroscopy. The experimental results showed that the adsorption equilibrium data were well
fitted to the Langmuir equation. The maximum adsorption capacity of the modified silicate material was 51.8 mg/g. The kinetic data
from the adsorption of phosphate were fitted to pseudo second-order model. The phosphate adsorption was highly pH dependent and
the relatively high removal of phosphate fell within the pH range 3.0–6.0. The coexistence of other anions in solutions has an adverse
e ect on phosphate adsorption; a decrease in adsorption capacity followed the order of exogenous anions: F?? > SO2?? 4 > NO??3 > Cl??. In
addition, the adsorbed phosphate could be desorbed by NaOH solutions. This silicate adsorbent with a large adsorption capacity and
relatively high selectivity could be utilized for the removal of phosphate from aqueous waste streams or in aquatic environment. 相似文献
334.
Soonchul Kwon Maohong Fan Herbert F. M. DaCost Armistead G. Russell 《环境科学学报(英文版)》2011,23(8):1233-1239
Olivine, one of the most abundant minerals existing in nature, is explored as a CO2 carbonation agent for direct carbonation of
CO2 in flue gas. Olivine based CO2 capture is thermodynamically favorable and can form a stable carbonate for long-term storage.
Experimental results have shown that water vapor plays an important role in improving CO2 carbonation rate and capacities. Other
operation conditions including reaction temperature, initial CO2 concentration, residence time corresponding to the flow rate of CO2
gas stream, and water vapor concentration also considerably affect the performance of the technology. 相似文献
335.
The Hg0 vapor adsorption experimental results on a novel sorbent obtained by impregnating a commercially available activated
carbon (Darco G60 from BDH) with silver nitrate were reported. The study was performed by using a fundamental approach, in an
apparatus at laboratory scale in which a synthetic flue gas, formed by Hg0 vapors in a nitrogen gas stream, at a given temperature
and mercury concentration, was flowed through a fixed bed of adsorbent material. Breakthrough curves and adsorption isotherms were
obtained for bed temperatures of 90, 120 and 150°C and for Hg0 concentrations in the gas varying in the range of 0.8–5.0 mg/m3. The
experimental gas-solid equilibrium data were used to evaluate the Langmuir parameters and the heat of adsorption. The experimental
results showed that silver impregnated carbon was very effective to capture elemental mercury and the amount of mercury adsorbed by
the carbon decreased as the bed temperature increased. In addition, to evaluate the possibility of adsorbent recovery, desorption was
also studied. Desorption runs showed that both the adsorbing material and the mercury could be easily recovered, since at the end of
desorption the residue on solid was almost negligible. The material balance on mercury and the constitutive equations of the adsorption
phenomenon were integrated, leading to the evaluation of only one kinetic parameter which fits well both the experimentally determined
breakthrough and desorption curves. 相似文献
336.
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340.
淀山湖沉积物碳-氮垂直分布特征 总被引:1,自引:0,他引:1
近年来,经过一系列污染治理措施,淀山湖的营养水平持续下降,但每年仍有不同程度的蓝藻水华暴发,严重影响其作为水源地的安全性。为了进一步探讨淀山湖水质改善策略,本研究对淀山湖沉积物营养状况进行了调查研究,分析了淀山湖沉积物碳、氮分布特征及垂直变化规律,并用沉积物肥力评价了淀山湖沉积物营养程度。结果表明,淀山湖沉积物营养盐存在明显的富集作用,二十多年来沉积物碳、氮含量大幅上升,表层沉积物均属于重污染状态。空间分布上,沉积物营养盐北部高,南部低,北部样点大部分属于重污染状态,南部样点基本属于中污染状态。垂直分布上,受航道回淤与北部围网养殖影响,部分样点营养盐垂直分布规律不显著,其他样点均表现出随深度增加营养盐显著降低的趋势。除出水口D1样点外,淀山湖有机质与TN表现出显著的同源相关性,表明有机质是淀山湖内源负荷的主要来源。 相似文献