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941.
活性炭辅助微波热解污泥反应条件的试验研究   总被引:1,自引:0,他引:1  
万立国  田禹  张丽君  方琳 《生态环境》2010,19(9):2182-2186
针对微波不能直接实现原污水污泥高温热解的问题,采用活性炭作为微波能吸收物质辅助污泥热解。对影响污泥热解效能的3个主要因素:污泥样品量、活性炭掺杂量和微波辐射功率,各做了3个水平的考察,得到了试验条件下的最优方案:污泥样品量30g、活性炭掺杂量6g、微波辐射功率1200W。结果表明:在最优试验方案下,污泥能在7min内升至920℃的高温,实现污泥快速、高效热解。通过分析3个因素对污泥热解效能的影响,进一步对最优试验方案下的固体产物吸收微波的性能及用其作为掺杂物辅助微波热解污水污泥的可行性进行了研究,结果表明:固体残渣吸收微波性能良好,可以代替活性炭作为更经济、高效的污泥微波热解辅助材料。  相似文献   
942.
稻草还田方式对双季稻田耕层土壤有机碳积累的影响   总被引:2,自引:0,他引:2  
选择南方典型双季稻田,研究不同的稻草还田方式对土壤不同层次有机碳的积累、表土碳密度、C/N比值及水稻产量的影响。结果表明,不同的稻草还田和耕作处理对水稻产量无显著影响;不同稻草还田处理的土壤有机碳和C/N均随土层加深而减小;3个稻草还田处理0-5 cm土层土壤有机碳质量分数显著高于不还田对照,其中,以高桩免耕处理最高,比无草翻耕处理提高13.8%(P〈0.01);5-10 cm土层表现为高桩翻耕处理显著高于其他处理,增加幅度为1.39-1.66 g kg-1;10-15 cm为翻耕处理(包括稻草不还田和还田)显著高于各免耕处理;稻草翻耕处理(0-15 cm)的耕层有机碳密度显著高于其他处理。因此,南方双季稻田采取稻草翻耕还田方式有利于增加土壤有机碳汇。  相似文献   
943.
The biologic activated carbon (BAC) process is widely used in drinking water treatments. A comprehensive molecular analysis of the microbial community structure provides very helpful data to improve the reactor performance. However, the bottleneck of deoxyribonucleic acid (DNA) extraction from BAC attached biofilm has to be solved since the conventional procedure was unsuccessful due to firm biomass attachment and adsorption capacity of the BAC granules. In this study, five pretreatments were compared, and adding skim milk followed by ultrasonic vibration was proven to be the optimal choice. This protocol was further tested using the vertical BAC samples from the full-scale biofilter of Pinghu Water Plant. The results showed the DNA yielded a range of 40 μg·g-1 BAC (dry weight) to over 100 μg·g-1 BAC (dry weight), which were consistent with the biomass distribution. All results suggested that the final protocol could produce qualified genomic DNA as a template from the BAC filter for downstream molecular biology researches.  相似文献   
944.
Chlorinated ethenes such as trichloroethene (TCE), cis‐1,2‐dichloroethene (cis‐1,2‐DCE), and vinyl chloride along with per‐ and polyfluoroalkyl substances (PFAS) have been identified as chemicals of concern in groundwater; with many of the compounds being confirmed as being carcinogens or suspected carcinogens. While there are a variety of demonstrated in‐situ technologies for the treatment of chlorinated ethenes, there are limited technologies available to treat PFAS in groundwater. At a former industrial site shallow groundwater was impacted with TCE, cis‐1,2‐DCE, and vinyl chloride at concentrations up to 985, 258, and 54 µg/L, respectively. The groundwater also contained maximum concentrations of the following PFAS: 12,800 ng/L of perfluoropentanoic acid, 3,240 ng/L of perfluorohexanoic acid, 795 ng/L of perfluorobutanoic acid, 950 ng/L of perfluorooctanoic acid, and 2,140 ng/L of perfluorooctanesulfonic acid. Using a combination of adsorption, biotic, and abiotic degradation in situ remedial approaches, the chemicals of concern were targeted for removal from the groundwater with adsorption being utilized for PFAS whereas adsorption, chemical reduction, and anaerobic biodegradation were used for the chlorinated ethenes. Sampling of the groundwater over a 24‐month period indicated that the detected PFAS were treated to either their detection, or below the analytical detection limit over the monitoring period. Postinjection results for TCE, cis‐1,2‐DCE, and vinyl chloride indicated that the concentrations of the three compounds decreased by an order of magnitude within 4 months of injection, with TCE decreasing to below the analytical detection limit over the 24‐month monitoring period. Cis‐1,2‐DCE, and vinyl chloride concentrations decreased by over 99% within 8 months of injections, remaining at or below these concentrations during the 24‐month monitoring period. Analyses of Dehalococcoides, ethene, and acetylene over time suggest that microbiological and reductive dechlorination were occurring in conjunction with adsorption to attenuate the chlorinated ethenes and PFAS within the aquifer. Analysis of soil cores collected pre‐ and post‐injection, indicated that the distribution of the colloidal activated carbon was influenced by small scale heterogeneities within the aquifer. However, all aquifer samples collected within the targeted injection zone contained total organic carbon at concentrations at least one order of magnitude greater than the preinjection total organic carbon concentrations.  相似文献   
945.
高俊炜  陈振乾 《化工环保》2016,36(6):661-665
采用巨正则蒙特卡罗方法模拟了CO_2在FAU分子筛上的吸附情况,比较了不同CO_2逸度下,CO_2在分子筛模型上的吸附位、吸附量的变化,拟合了其吸附等温线。结果表明:在吸附饱和状态下,分子筛的孔结构越大,对CO_2的吸附量越大,对于比CO_2分子更小的微孔结构,吸附几乎不发生;在低逸度下,CO_2的吸附主要发生在小孔内,随着逸度的提高,CO_2的吸附量迅速上升;在高逸度下,吸附量的提高主要发生在大孔内;FAU分子筛吸附CO_2的过程符合Ⅰ型Langmuir吸附等温线,在高压下对CO_2的吸附能力远大于低压下的吸附能力。  相似文献   
946.
The study aimed to find out the influence of sweating on footwear insulation with a thermal foot model. Simultaneously, the influence of applied weight (35 kg), sock, and steel toe cap were studied. Water to 3 sweat glands was supplied with a pump at the rate of 10 g/hr in total. Four models of boots with steel toe caps were tested. The same models were manufactured also without steel toe. Sweating reduced footwear insulation 19–25% (30–37% in toes). During static conditions, only a minimal amount of sweat evaporated from boots. Weight affected sole insulation: Reduction depended on compressibility of sole material. The influence of steel toe varied with insulation. The method of thermal foot model appears to be a practical tool for footwear evaluation.  相似文献   
947.
焦化废水的处理一直是国内外废水处理领域的难题之一。文章以宝钢为例,介绍并分析了该企业焦化废水处理技术的发展与现状。  相似文献   
948.
根据联合国政府间气候变化专门委员会推荐的方法,计算了秦皇岛市工业行业2005-2010年的能源消费碳排放。秦皇岛市工业效益偏低,重工业比例偏大和以煤炭为主的能源结构是碳排总量和碳排放强度的主要驱动力。改造提升传统主导产业,做强装备制造业,加快工业园区建设,完善产业链,改善能源结构等是秦皇岛市工业产业结构优化的主要途径。  相似文献   
949.
李璇  姚建  杨柳  苏维 《四川环境》2013,32(2):60-63
低碳技术可分为3类:减碳技术、无碳技术、去碳技术,选择最优低碳技术是一个项目能否成功的关键。低碳技术评价的内容通常从能源使用率、经济效益、生命周期方面进行评价,对技术的综合性评价的基本方法大致有层次分析法、综合评分法、德尔菲法、熵值法、模糊综合评判法等,这些方法渗透于指标权重分析、模型建立评价当中。通过研究对这些技术的评价方法,确定最优的技术项目,以促进循环经济及可持续发展战略的实施和进行。  相似文献   
950.
针对油田采出废水的特点,以粘胶基活性炭纤维为原料,经二次炭化和二次活化方式处理制得ACF样品。以ACF为过滤材料,对延长某采油厂经过沉降、分离处理后的采油废水进行动态吸附实验,实验结果表明:经水蒸汽二次活化得到的ACF样品对选用的油田废水处理效果最佳,其悬浮物颗粒粒径中值0.496μm(<1.0μm)、悬浮物含量为0.77mg/L(<1.0mg/L)。  相似文献   
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