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961.
在硫酸系统中,通过水平衡分析计算烟气带入净化工序的SO2体积分数和含水量,确定净化工序的能力,控制干燥塔进口烟气温度,使干吸工序生产出合格产品;通过计算,烟气带入净化工序的水量小于产品带出的水量,制酸净化污水经过污水处理工序处理后返回到净化工序重复使用,实现净化污水零排放,消除对环境的污染. 相似文献
962.
963.
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
964.
This work was designed to explore the characteristics of photodegradation of herbicides in the copper-polluted water body. The
results showed that Cu(II) alone could induce a photo Fenton-like reaction to enhance the degradation of atrazine, in which hydroxyl
radical ( OH) was a main active species. Humic acids restrained atrazine degradation, nevertheless, when introducing Cu(II), the
photodegradation was accelerated, in which singlet oxygen (1O2) replaced OH acting as the prevailing species. A feasible mechanism
for the photochemical process was also proposed, which is helpful for better understanding the environmental photochemistry of
atrazine in the copper-polluted water. 相似文献
965.
Seepage from Hg mine wastes and calcines contains high concentrations of mercury (Hg). Hg pollution is a major environmental
problem in areas with abandoned mercury mines and retorting units. This study evaluates factors, especially the hydrological and
sedimentary variables, governing temporal and spatial variation in levels and state of mercury in streams impacted by Hg contaminated
runo . Samples were taken during di erent flow regimes in theWanshan Hg mining area in Guizhou Province, China. In its headwaters
the sampled streams/rivers pass by several mine wastes and calcines with high concentration of Hg. Seepage causes serious Hg
contamination to the downstream area. Concentrations of Hg in water samples showed significant seasonal variations. Periods of
higher flow showed high concentrations of total Hg (THg) in water due to more particles being re-suspended and transported. The
concentrations of major anions (e.g., Cl??, F??, NO3?? and SO4
2??) were lower during higher flow due to dilution. Due to both sedimentation
of particles and dilution from tributaries the concentration of THg decreased from 2100 ng/L to background levels (< 50 ng/L) within
10 km distance downstream. Sedimentation is the main reason for the fast decrease of the concentration, it accounts for 69% and 60%
for higher flow and lower flow regimes respectively in the upper part of the stream. Speciation calculation of the dissolved Hg fraction
(DHg) (using Visual MINTEQ) showed that Hg(OH)2 associated with dissolved organic matter is the main form of Hg in dissolved
phase in surface waters in Wanshan (over 95%). 相似文献
966.
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
967.
Achour Terbouche Chafia Ait Ramdane-Terbouche Didier Hauchar Safia Djebbar 《环境科学学报(英文版)》2011,23(7):1095-1103
The adsorption capacities of new humic acids isolated from Yakouren forest (YHA) and Sahara (Tamenrasset: THA) soils (Algeria)
and commercial humic acid (PFHA) on polyaniline emeraldine base (PEB) were studied at pH 6.6. Also the adsorption of heavy
metals such as Cd2+, Zn2+ and Ni2+ on humic acid-polyaniline systems (HA-PEB) was investigated at the same conditions. HA-PEB
compounds were characterized by scanning electron microscopy (SEM), infrared spectrometry and cavity microelectrode. In addition,
batch adsorption and cavity microelectrode were used in the adsorption study of Cd2+, Zn2+ and Ni2+ on HA-PEB. To develop biocaptors
of polluting metals using a cavity microelectrode modified by HA-PEB systems, the adsorption kinetic and adsorption capacity were
investigated. The SEM analysis showed that the presence of humic acid affected the PEB surface and caused the formation of a
granular morphology. The maximum adsorption capacities (qmax) of PFHA, THA and YHA determined by adsorption isotherms were
91.31, 132.1 and 151.0 mg/g, respectively. Batch adsorption results showed that qmax of Cd2+, Zn2+ and Ni2+ on HA-PEB followed
the order: THA-PEB > YHA-PEB > PFHA-PEB. The voltammograms obtained with HA-PEB modified cavity microelectrode showed
the appearance of new redox couples reflecting the adsorption of HA on PEB. Metal-humic acid-polyaniline voltammograms were
characterized by appearance of oxidation-reduction couples or reduction wave corresponding to metal. Finally, the result may be
exploited to develop a biocaptor based on the cavity microelectrode amended by THA-PEB and YHA-PEB. 相似文献
968.
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
969.
Potassium-modified ceria-zirconia catalyst was synthesized by wetness impregnation method. The ageing treatment was performed in static air at 800℃ for 20 hr to evaluate the thermal stability of the catalyst. The catalysts were characterized by X-ray diffraction,BET surface area, oxygen storage capacity, NOx-temperature programmed desorption and soot-temperature programmed oxidation measurements. By introduction of potassium, the maximum soot oxidation rate temperature (Tm) of the ceria-zirconia based catalyst decreased from 525 to 428℃ in the presence of NO under a loose contact mode. The shift of Tm of the K-modified catalyst after ageing is only 15℃. The enhanced activity of the aged catalyst mainly lies in the promotional effect of potassium on the NOx/oxygen storage cacity as well as the soot-catalyst contact. 相似文献
970.