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161.
Fe~(3+)掺杂TiO_2/凹凸棒复合材料的光催化性能   总被引:1,自引:1,他引:1  
采用酸催化的溶胶-凝胶法制备了一系列Fe3+掺杂TiO2/凹凸棒(Fe3+-TiO2/ATP)复合光催化剂材料。在可见光条件下,以亚甲基蓝(MB)溶液的光催化降解反应,评价了样品的光催化性能,研究了TiO2负载量、Fe3+掺杂量和焙烧温度对复合材料光催化性能的影响。在单因素实验的基础上,采用正交实验设计(L25(53))优化了催化剂的制备条件。光催化实验结果表明,MB在复合材料上的光催化降解反应遵循Langmuir-Hinshelwood(L-H)动力学模型。正交实验结果表明,当TiO2负载量为15%、Fe3+掺杂量为0.5%和焙烧温度为550℃时,得到的复合材料对MB的光催化降解效率最佳,测得表观反应速率常数kapp为6.09×10-3min-1,反应4 h后MB的降解率(Dt)可达75.88%,相同实验条件下与P25(1.51×10-3min-1)相比较,反应速率提高了4.03倍,降解率提高了45.05%。另外,复合材料的沉降性能优于P25,易于分离,是一类有应用前景的复合光催化剂。  相似文献   
162.
不同龄渗滤液及其在包气带中的迁移转化研究   总被引:1,自引:0,他引:1  
通过实验室土柱模拟方法,研究了不同场龄渗滤液中有机污染物、氮以及 Fe、Mn、Zn、Cd 在包气带中的迁移转化规律.结果表明,不同场龄渗滤液理化性质差别很大,随着场龄的增加,COD 从40 194 mg/L降低到 1 778 mg/L,NH4 浓度从1 758 mg/L升高到2 166 mg/L,金属浓度则减小.经过以细砂为介质的包气带后,新渗滤液易对地下水造成高浓度有机物污染,而老渗滤液更容易造成地下水的高浓度氮污染.Fe、Mn 和 Cd 在包气带中比较稳定,而 Zn 的迁移能力很强,易对地下水构成威胁.  相似文献   
163.
Journal of Material Cycles and Waste Management - The preparation of alkali-activated materials from red mud for building materials is a promising way to solve the environmental pollution caused by...  相似文献   
164.
苯酚分子印迹聚合物的合成、表征及吸附性能研究   总被引:1,自引:0,他引:1  
以苯酚为模板,2-Vpy为功能单体,EGDMA为交联剂,采用本体聚合方式在氯仿溶剂中合成了一系列分子印迹聚合物,并通过静态吸附实验对聚合物的选择吸附性进行评价.结果显示,以氯仿作为致孔剂,模板分子与功能单体的摩尔比为1∶2时,聚合物对模板分子的印迹因子为3.96,最大表现结合量(Qmax)为120.7 mmol/g,具...  相似文献   
165.
采用浸渍法制备了Ca(Ⅱ)-AgNbO3光催化剂,并运用XRD、FT-IR、DRS、XPS和SEM对催化剂进行表征和分析.实验以亚甲基蓝为模拟污染物,在紫外光下考察Cu(Ⅱ)掺杂对AgNbO3光催化效果的影响.分析显示,掺杂Cu(Ⅱ)后AgNbO3晶型及表面形貌没有发生变化,但在可见光区的吸光度得到有效提高.光催化脱色结果表明,当Cu(Ⅱ)的掺杂量为2%(质量比),热处理温度为300℃,催化剂用量为1 g/L,亚甲基蓝初始浓度为10 mg/L,溶液pH值为7.15时,Cu(Ⅱ)-AgNbO3紫外光催化亚甲基蓝脱色的效果最好,3 h后,亚甲基蓝脱色率可达97.1%.  相似文献   
166.
在全球气候变暖和能源危机的背景下,农业是温室气体主要排放源之一,低碳农业作为应对气候变化的农业行动,越来越受到人们的重视。低碳农业的目标是减缓温室气体,实现高效率、低能耗、低排放、高碳汇的高效农业。在推动我国低碳农业发展的措施方面,总结起来主要包括减少碳排放、增加碳汇和采用其他相应的技术措施相结合。也就是通过一系列相应的技术措施和基础设施建设,减少温室气体总量排放的同时,增加耕地、草地和林地吸收二氧化碳的量,从而实现低碳农业的可持续发展。  相似文献   
167.
Abstract

A high-efficiency particulate air (HEPA)-carbon filtration system was developed by the Access Business Group, LLC, to reduce the indoor levels of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs). The HEPA filter removes the particle-bound PCDD/Fs, and the carbon filter removes the gaseous fraction. Because of the toxicity of PCDD/Fs, it is very difficult to handle them in the laboratory. In this study, mathematical modeling was performed to evaluate the performance of the HEPA-carbon filtration system for PCDD/Fs removal and to optimize its design and operation. The model was calibrated with experimental data conducted with toluene in a sealed room. Model simulations with four selected congeners demonstrated that it takes ~1 hr for the indoor air treatment system to reach the maximum removal efficiency and that the carbon air filter has a life time of 107 yr for dioxin removal. Given a zero emission from the HEPA filter, the overall removal efficiency is 78.7% for 2,3,7,8-tetrachloro dibenzo-p-dioxins, 89.8% for octa-chlorodibenzodioxin, 78% for tetra-chlorodibenzofuran, and 89.8% for octachlorodibenzofuran. The larger the mass emission from the HEPA filter, the lower the overall removal efficiency, and the larger the ratio of the filter flow rate (Qf) to the room flow rate (Q), the higher the overall removal efficiency. When the ratio of Qf/Q is 15, an overall removal efficiency of 90% can be reached for all four of the selected compounds. The removal of the four selected compounds does not change as the relative humidity increases ≤90%.  相似文献   
168.
● P-rich carp residues-derived biochars presented excellent Cu sorption capacity. ● Sorption mechanisms of Cu on CRBs were mainly precipitation and surface complexation. ● CRBs could immobilize Cu and reduce its bioavailability in aquatic environment. Heavy metal pollution has attracted worldwide attention because of its adverse impact on the aquatic environment and human health. The production of biochar from biowaste has become a promising strategy for managing animal carcasses and remediating heavy metal pollution in the aquatic environment. However, the sorption and remediation performance of carp residue-derived biochar (CRB) in Cu-polluted water is poorly understood. Herein, batches of CRB were prepared from carp residues at 450–650 °C (CRB450–650) to investigate their physicochemical characteristics and performance in the sorption and remediation of Cu-polluted water. Compared with a relatively low-temperature CRB (e.g., CRB450), the high-temperature biochar (CRB650) possessed a large surface area and thermodynamic stability. CRB650 contained higher oxygen-containing functional groups and P-associated minerals, such as hydroxyapatite. As the pyrolytic temperature increased from 450 to 650°C, the maximum sorption capacity of the CRBs increased from 26.5 to 62.5 mg/g. The adsorption process was a type of monolayer adsorption onto homogenous materials, and the sorption of Cu2+ on the CRB was mainly based on chemical adsorption. The most effective potential adsorption mechanisms were in order of electrostatic attraction and cation-π interaction > surface complexation and precipitation > pore-filling and cation exchange. Accordingly, the CRBs efficiently immobilized Cu2+ and reduced its bioavailability in water. These results provide a promising strategy to remediate heavy metal-polluted water using designer biochars derived from biowastes, particularly animal carcasses.  相似文献   
169.
企业是践行可持续理念、实现可持续发展目标的重要主体。企业需要在生产经营过程中统筹提升环境(E)、社会(S)、治理(G)三个维度的ESG绩效。基于外部压力和内部实力,本文预先设定了国家背景、行业属性、金融实力三种因素驱动企业改善ESG绩效的理论假设。为检验假设,本文使用多元线性回归和多层线性模型对来自55个国家、共计6139家上市公司样本进行实证研究。结果表明,即使在控制企业规模、风险管理和社会声誉的情况下,国家可持续发展水平、行业绿色发展水平、企业金融实力仍能显著提升企业ESG绩效。其中,国家和行业变量不仅直接促进了企业ESG绩效的提升,还在更高维度上通过调节CFP-ESG的关系间接促进企业ESG绩效的提升。本研究有助于企业更好地制定实施可持续发展战略,也能为投资者评估并筛选出ESG绩效优异的企业提供科学参考。  相似文献   
170.
To improve the desulfurization efficiency of sorbents at low cost, modified semi-coke was used as the substrate for mixed metal oxides (ZFM; oxides of zinc [Zn], iron [Fe], and manganese [Mn]) in hot gas desulfurization. Performance of the prepared ZFM/modified semi-coke (MS) sorbents were evaluated in a fixed-bed reactor in the temperature range 400-550°C. Results showed that the molar ratio of Mn to Zn, effect of the substrate, the calcination temperature, and the sulfidation temperature influenced the performance of the sorbents. Optimum conditions for the preparation of the ZFM/MS sorbents were molar ratio of Mn(NO(3))(2)·6H(2)O, Zn(NO(3))(2), and Fe(NO(3))(3), 0.6:1:2; mass ratio of ZFM0.6 to modified semi-coke support, 1:1; and calcination temperature, 600°C. The ZFM0.6/MS sorbent thus prepared exhibited the best sorption sulfur capacity of 27.46% at 450°C.  相似文献   
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