全文获取类型
收费全文 | 250篇 |
免费 | 11篇 |
国内免费 | 89篇 |
专业分类
安全科学 | 24篇 |
废物处理 | 2篇 |
环保管理 | 24篇 |
综合类 | 164篇 |
基础理论 | 59篇 |
环境理论 | 1篇 |
污染及防治 | 39篇 |
评价与监测 | 24篇 |
社会与环境 | 8篇 |
灾害及防治 | 5篇 |
出版年
2024年 | 2篇 |
2023年 | 15篇 |
2022年 | 12篇 |
2021年 | 10篇 |
2020年 | 14篇 |
2019年 | 13篇 |
2018年 | 12篇 |
2017年 | 8篇 |
2016年 | 11篇 |
2015年 | 21篇 |
2014年 | 19篇 |
2013年 | 15篇 |
2012年 | 16篇 |
2011年 | 21篇 |
2010年 | 8篇 |
2009年 | 17篇 |
2008年 | 13篇 |
2007年 | 11篇 |
2006年 | 14篇 |
2005年 | 13篇 |
2004年 | 12篇 |
2003年 | 11篇 |
2002年 | 12篇 |
2001年 | 10篇 |
2000年 | 11篇 |
1999年 | 5篇 |
1998年 | 4篇 |
1997年 | 1篇 |
1996年 | 9篇 |
1995年 | 1篇 |
1994年 | 4篇 |
1993年 | 2篇 |
1992年 | 1篇 |
1983年 | 1篇 |
1973年 | 1篇 |
排序方式: 共有350条查询结果,搜索用时 46 毫秒
51.
草场管理中的市场机制与习俗制度的关系及其影响:青藏高原案例研究 总被引:1,自引:1,他引:0
近年来,政府大力推动在完善承包到户基础上的草场经营权的流转,目的之一是通过市场手段来整合牧户个体的草场资源,促进畜牧业的规模化生产。市场机制与牧区传统管理草场的习俗制度,二者的关系及其对草场管理的影响是怎样的?论文选择位于青海省贵南县的元义村和查乃核村为案例地来研究上述问题。元义村反映市场机制取代习俗制度,查乃核村则反映了市场机制嵌套在习俗制度中。通过比较两个案例地的牧户生计、畜牧业生产以及贫富差距,研究发现:1)查乃核村的牧户年均畜牧业资产高于元义村;2)查乃核村的畜牧业生产量逐年增加、牲畜死亡率明显减少,畜牧业生产收益率高于元义村;3)查乃核村的贫富差距明显低于元义村。基于此,论文认为市场机制嵌套在社区习俗制度的制度安排在草场管理中更有效,因为这样的管理模式在满足牧户个体对于权属明晰和补偿需求的同时,能够维持社区共用草场以适应青藏高原多变的气候特征所导致的资源时空分布的异质性。随着市场化的发展,草场管理需要权属明晰及市场机制,但实现这样的目标不需要弱化甚至取代已有的社区习俗制度。 相似文献
52.
53.
三种厌氧促进剂对亚铵废液厌氧发酵的影响 总被引:4,自引:0,他引:4
根据亚铵法草浆蒸煮废液的间歇式厌氧发酵试验结果,分析了活性炭、硫酸亚铁和膨润地亚胺废液厌氧发酵的影响。结果表明,当投量为2.5g/L时,34种耨氧促进剂都能显著地促进亚铵废液的厌氧发酵;与对照试验相比,可将厌氧系统的30d累积产气量分别提高16.1%、13.9%和26.1%。本研究还初步探讨了这3种厌氧促进剂的作用机理。 相似文献
54.
In this study, stabilized Pd, Pt and Au nanoparticles were successfully prepared in aqueous phase using sodium carboxymethyl cellulose (CMC) as a capping agent. These metal nanoparticles were then tested for catalytic hydrodechlorination toward two classes of organochlorinated compounds (vinyl polychlorides including trichloroethylene (TCE), tetrachloroethylene (PCE), and alkyl polychlorides including 1,1,1-trichloroethane (1,1,1-TCA), and 1,1,1,2-tetrachloroethane (1,1,1,2-TeCA)) to determine the rate-limiting steps and to explore the reaction mechanisms. The surface area normalized reaction rate constant, kSA, showed a systematic dependence on the electronic structure (the density of states at the Fermi level) of the metals, suggesting that adsorption of organochlorinated reactants on the metal catalyst surfaces is the rate-limiting step for catalytic hydrodechlorination. Hydrodechlorination rates of 1,1,1-TCA and 1,1,1,2-TeCA agreed with the bond strength of the first (weakest) dissociated C-Cl bond, suggesting that C-Cl bond cleavage, which is the first step for dissociative adsorption of the alkyl polychlorides, controlled the catalytic hydrodechlorination rate. However, hydrodechlorination rates of TCE and PCE correlated with the adsorption energies of their molecular (non-dissociative) adsorption on the noble metals rather than with the first C-Cl bond strength, suggesting that molecular adsorption governs the reaction rate for hydrodechlorination of the vinyl polychlorides. 相似文献
55.
从基层林业企业安全教育管理现状出发,分析了当前安全教育管理存在的问题,结合新形势下林业企业实际,探索创新安全生产管理路径与措施。 相似文献
56.
Qing Xia Deyang Kong Guoqiang Liu Qingguo Huang Aamr Alalewi Junhe Lu 《Frontiers of Environmental Science & Engineering》2014,8(3):372-378
The removal of 17β-estradiol (E2) in laccase catalyzed oxidative coupling processes was systematically studied in this work. We focused on the influence of pH and natural organic matter (NOM) on the performance of the enzymatic treatment processes. It was found that the optimal pH for E2 removal was between 4 and 6. The removal of E2 was slightly inhibited in the presence of NOM. Enzymatic transformation of E2 was second-order in kinetics with first-order to both the concentrations of the enzyme and contaminant. Mass spectrum (MS) analysis suggested that coupling products were formed through radical-radical coupling mechanism. The results of this study demonstrated that laccase catalyzed oxidative coupling process could potentially serve as a treatment strategy to control steroid estrogens. 相似文献
57.
58.
Optimal regulation of a polluting natural monopolist must correct for both external damages and market power to achieve a social optimum. Existing non-Bayesian regulatory methods require knowledge of the demand function, while Bayesian schemes require knowledge of the underlying cost distribution. We introduce mechanisms adapted to use less information. Our Price-based Subsidy (PS) mechanisms give the firm a transfer that matches or approximates the incremental surplus generated each period. The regulator need not observe the abatement activity or know the demand, cost, or damage functions of the firm. All of the mechanisms induce the firm to price at marginal social cost, either immediately or asymptotically. 相似文献
59.
探讨了新时期南京城郊结合部拓展的特征与机制。南京城郊结合部拓展的特征表现为以下方面:在经济发展上,城郊结合部发展速度高于远郊县,但低于城区;在人口城市化上,是人口增长最快的地区;在土地利用上,城郊结合部粗放发展。就拓展机制而言,认为当前南京城郊结合部的拓展主要是由城市向郊区分散发展的新战略、巨型工程的建设和行政区划调整等力量的驱动。目前,快速发展的南京城郊结合部也面临很多问题,诸如用地粗放、城中村问题、基础设施和服务设施建设滞后、对生态和开敞空间的侵占等。认为这些问题的根源在于两个方面--城乡双轨体制造成的政策缺位和郊区政府的企业化行为。最后,对优化南京城郊结合部的发展提出若干建议。这些建议包括创新制度,消除城乡壁垒;有机疏散,有效控制城市蔓延;引导城郊结合部房地产和大学城的发展;加强外来人口管理,采用激活的方式改造城中村。 相似文献
60.
Nowadays, iron ions as a ubiquitous heavy metal pollutant are gradually concerned and the convenient and quick removal of excessive iron ions in groundwater has become a major challenge for the safety of drinking water. In this study, boron-doped biochar (B-BC) was successfully prepared at various preparation conditions with the addition of boric acid. The as-prepared material has a more developed pore structure and a larger specific surface area (up to 897.97 m²/g). A series of characterization results shows that boric acid effectively activates biochar, and boron atoms are successfully doped on biochar. Compared with the ratio of raw materials, the pyrolysis temperature has a greater influence on the amount of boron doping. Based on Langmuir model, the maximum adsorption capacity of 800B-BC1:2 at 25 °C, 40 °C, 55 °C are 50.02 mg/g, 95.09 mg/g, 132.78 mg/g, respectively. Pseudo-second-order kinetic model can better describe the adsorption process, the adsorption process is mainly chemical adsorption. Chemical complexation, ions exchange, and co-precipitation may be the main mechanisms for Fe2+ removal. 相似文献