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131.
溶液吸收/分光光度法检测空气中偏二甲肼含量 总被引:1,自引:0,他引:1
GJB2373-95采用固体吸附/分光光度法监测空气中偏二甲肼,但是采集空气中偏二甲肼所用的SG-2固体吸附剂和采样管制作繁琐,分析步骤复杂,不适合连续监测。文章以单位自行研制的偏二甲肼动态配气系统配制已知浓度空气样品为测试环境,用标定过的美国Interscan气体检测仪实时监测其浓度为13.4×10-6~13.6×10-6,采用溶液吸收法采样并简化GJB2373-95标准方法的分析步骤。依据两种方法分别做出各自的标准曲线,并采用固体吸附法和溶液吸收法各采集两个平行样,样品采样体积分别为3.28L、3.31L和3.12L、3.14L,对应各自的标准曲线,计算出两组样品偏二甲肼含量分别为10.7×10-6、11.0×10-6和12.1×10-6、12.0×10-6。经传感器实时监测值作为第三方数据比对,结果表明溶液吸收/分光光度法监测结果准确,分析步骤简单、省时。 相似文献
132.
Enhanced adsorption of Methylene Blue from aqueous solution by chitosan-g-poly (acrylic acid)/vermiculite hydrogel composites 总被引:2,自引:1,他引:1
A series of chitosan-g-poly (acrylic acid)/vermiculite hydrogel composites were synthesized and used as adsorbents for the
investigation of the e ect of process parameters such as vermiculite content, pH of dye solution, contact time, initial concentration
of dye solution, temperature, ionic strength and concentration of surfactant sodium dodecyl sulfate on the removal of Methylene Blue
(MB) from aqueous solution. The results showed that the adsorption capacity for dye increased with increasing pH, contact time
and initial dye concentration, but decreased with increasing temperature, ionic strength and sodium dodecyl sulfate concentration in
the present of the surfactant. The adsorption kinetics of MB onto the hydrogel composite followed pseudo second-order kinetics and
the adsorption equilibrium data obeyed Langmuir isotherm. By introducing 10 wt.% vermiculite into chitosan-g-poly (acrylic acid)
polymeric network, the obtaining hydrogel composite showed the highest adsorption capacity for MB, and then could be regarded as a
potential adsorbent for cationic dye removal in a wastewater treatment process. 相似文献
133.
无铅焊料合金中重金属元素浸出行为的研究 总被引:1,自引:0,他引:1
选用Sn.3.5Ag-0.5Cu、Sn-3.5Ag、Sn-0.5Cu无铅焊料合金及它们与Cu的钎焊接头,研究了它们在典型的酸性、碱性和盐溶液中的重金属元素的浸出规律.结果表明,焊料合金中的主要浸出元素Sn在酸性或碱性溶液中的浸出量都不是太多,而在NaCl盐溶液中浸出量增大2个数量级.制备成钎焊接头后,在酸性环境中,Sn-3.5Ag和Sn.0.5Cu钎焊接头中Sn的浸出量增加1个数量级以上,而在NaOH碱性环境中.Sn-3.5Ag-0.5Cu钎焊接头中Sn的浸出量相对较高.该结果对电子垃圾填埋环境选择及相关决策提供了参考. 相似文献
134.
Impacts of soil organic matter, pH and exogenous copper on sorption behavior
of norfloxacin in three soils 总被引:3,自引:0,他引:3
ZHANG Jie LI Zhaojun GE Gaofei SUN Wanchun LIANG Yongchao WU Laosheng 《环境科学学报(英文版)》2009,21(5):632-640
Norfloxacin (Nor) sorption and the factors (soil organic matter (SOM), pH, and exogenous copper (Cu) influencing the sorption were investigated in a black soil (soil B), a fluvo-aquic soil (soil F), and a red soil (soil R). With increasing of Nor concentrations, sorption amount of norfloxacin increased in both the bulk soils and their SOM-removed soils, but the sorption capacity in SOM-removed soils was higher than that of their corresponding bulk soils, indicating that the process of norfloxacin sorption in soil was influenced by the soil properties including SOM. The sorption data in all bulk soils and SOM-removed soils were fitted to Freundlich and Langmuir models. The correlation coefficients suggested that the experimental data fitted better to Freundlich equation than to Langmuir equation. Furthermore, the data from soil F and SOM-removed F could not be described by Langmuir equation. The norfloxacin sorption amount decreased in soil B and soil F, whereas it increased in soil R as solution pH increased. The maximum KD and KOC were achieved in soil R when the equilibrium solution pH was 6. And the norfloxacin sorption was also influenced by the exogenous Cu2+ ions, which depended on the soil types and Cu2+ concentrations. With increasing of Cu2+ concentrations in solution, generally, sorption amount, KD and KOC for norfloxacin in soils increased and were up to a peak at 100 mg/L Cu2+, and then the sorption amount decreased regardless of norfloxacin levels. 相似文献
135.
136.
为准确预测煤层气中多组分气体的吸附性能,将空位溶液与Dubinbin-Astakhov(DA)理论相结合,提出1种适用于煤层气吸附系统的多组分混合吸附模型。在模型中,吸附体系被视为气体与假设的“空位溶质”的多元混合物,吸附体系视为气相和吸附相空位溶质之间的平衡。结果表明:根据单组分气体吸附等温线,采用D-A方程计算分析了生成二元(吸附质+空位)混合物中纯组分气体的活度系数,并优化吸附参数;模型能够根据在单一温度下收集的纯组分吸附数据预测不同温度下的多组分气体吸附;模型计算结果与实测结果吻合良好,误差在10%以内,充分说明模型是切实可靠的。 相似文献
137.
The biosorption characteristics of Cs(I) ions from aqueous solution using exopolymers (PFC02) produced from Pseudomonas
fluorescens C-2 were investigated as a function of pH, biosorbent dosage, contact time and initial concentration. pH played a major role
in the adsorption process, and the optimum pH for the removal of Cs(I) was 8.0. Langmuir, Freundlich and Dubinin-Radushkevich (D-R)
models were applied to describe the biosorption isotherm of the Cs(I) ions by PFC02. The Lagergren first-order, pseudo second-order
kinetic and intraparticle diffusion models were used to test the kinetic data. Langmuir model and D-R model fitted the equilibrium data
better than the Freundlich isotherm. The monolayer adsorption capacities of PFC02 as obtained from Langmuir isotherm at 25°C was
found to be 32.63 mg/g. From the D-R isotherm model, the mean free energy was calculated as 26.73 kJ/mol, indicating that the
biosorption of cesium was chemisorption. The biosorption process was rapid, and the kinetic rates were best fitted to the pseudo
second-order model, which indicated the biosorption process operated through chemisorption mechanism. FT-IR analysis of PFC02
showed the possible functional groups responsible for cesium adsorption were hydroxyl, carboxyl, carbonyl and sulphonate groups.
SEM analysis showed the porous structure of the material while EDX analysis confirmed the adsorption of Cs(I) on PFC02. Cesium
adsorbed onto the PFC02 could be desorbed efficiently using 1 mol/L HNO3, and the enrichment factor was 50.0. Furthermore, PFC02
could be reused five times with only about 8.25% regeneration loss. The developed method was successfully utilized for the removal of
Cs(I) ions from aqueous solution. 相似文献
138.
Material conversion from paper sludge ash (PSA) in NaOH solution was attempted to synthesize the adsorbent for removal of
inorganic pollutants, such as Pb2+, NH4
+ and PO4
3?? from aqueous solution. PSA of 0.5 g was added into 10 mL of 3 mol/L NaOH
solution, and then heated at 80, 120, and 160°C for 6–48 hr to obtain the product. PSA mainly composed of two crystalline phases,
gehlenite (Ca2Al2SiO7) and anorthite (CaAl2Si2O8), and amorphous phase. Hydroxysodalite (Na6Al6Si6O24 8H2O) was formed at
80°C, and anorthite dissolved, whereas gehlenite remained una ected. Katoite (Ca3Al2SiO4(OH)8) was formed over 120°C, and
hydroxycancrinite (Na8(OH)2Al6Si6O24 2H2O) was formed at 160°C, due to the dissolution of both gehlenite and anorthite. Specific
surface areas of the products were almost same and were higher than that of raw ash. Cation exchange capacities (CECs) of the products
were also higher than that of raw ash, and CEC obtained at lower temperature was higher. Removal abilities of products for Pb2+, NH4
+,
and PO4
3?? were higher than that of raw ash.With increasing reaction temperature, the removal e ciencies of Pb2+ and NH4
+ decreased
due to the decrease of CEC of the product, while removal e ciency for PO4
3?? was almost same. The concentrations of Si and Al in the
solution and the crystalline phases in the solid during the reaction explain the formation of the product phases at each temperature. 相似文献
139.
140.
为明确煤尘粒径对表面活性剂复配溶液润湿能力的影响,以径长范围为小于74、74~104、104~147μm的3种红柳煤样为研究对象,开展沉降试验。选取十二烷基硫酸钠(SDS)、脂肪酸甲酯乙氧基化物磺酸盐(FMES)、脂肪醇聚氧乙烯醚硫酸钠(AES)、异辛醇聚氧乙烯醚(JFC)和辛癸基葡糖苷(APG)5种表面活性剂,将其以质量比1∶1两两复配成10种复配组合,分别对单体和复配溶液作沉降试验,探究不同粒径煤尘在复配溶液和组成它们的表面活性剂单体溶液中的沉降速度变化特征。结果表明:煤尘粒径不会影响表面活性剂之间的协同润湿作用,但会影响表面活性剂之间的协同润湿程度;不同复配组合之间的润湿能力强弱不因煤尘粒径改变而变化;相较小粒径煤尘,复配溶液质量分数提高对大粒径煤尘润湿能力的提升更为明显;SDS与JFC复配组合对不同粒径煤尘均有很好的润湿效果,通过表面活性剂处理前后煤样的红外光谱分析推测,SDS与JFC能够协同提高煤尘的润湿性。 相似文献