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51.
采用浸渍法制备了一系列不同钒和钨负载量的V2O5-WO3/TiO2催化剂样品,对样品NH3选择性催化还原NO性能进行了评价,并用BET、XRD、XPS等手段对催化剂样品的表面形态进行了表征.研究发现,钒的负载量对催化剂的比表面积和催化活性有显著影响,当钒负载量从1%升高到8%时,催化剂比表面积下降了16 m2/g,最高活性温度降低了约100℃.钨起到稳定剂和助剂的双重作用,当钒负载量为1%时,钨负载量从0升高到6%,催化剂比表面积仅下降了3 m2/g,而活性温度窗口向高温和低温各拓宽了约50℃.研究表明钒和钨负载量都能影响催化剂表面的VOx物种,但对催化剂的表面晶型没有明显影响.  相似文献   
52.
A series of single-phase T-structured NdSrCu_(1-x)Co_xO_(4-δ) with oxygen vacancies and T'-structured Sm_(1.8)Ce_(0.2)Cu_(1-x)Co_xO_(4-δ) (x:0-0.4) with oxygen excess were prepared using ultrasound-assisted citric acid complexing method, and characterized by means of techniques such as thermogravimetric analysis and NO temperature-progranuned desorption (NO-TPD). The catalytic activities of these materials were evaluated for the decomposition of NO. It was found that the NdSrCut_xCoxO4_b catalysts were of oxygen vacancies whereas the Sm_(1.8)Ce_(0.2)CU_(1-x)Co_xO_(4-δ) ones possessed excessive oxygen (i.e., over-stoichiometric oxygen); with a rise in Co doping level,the oxygen vacancy density of NdSrCu_(1-x)Co_xO_(4-δ) decreased while the over-stoichiometric oxygen amount of Sm_(1.8)Ce_(0.2)CU_(1-x)Co_xO_(4-δ)increased. The NO-TPD results revealed that NO could be activated much easier over the oxygen-deficient perovskite-like oxides than over the oxygen-excessive perovskite-like oxides, with the NdSrCuO_(3.702) catalyst showing the best efficiency in activating NO molecules. Under the conditions of 1.0% NO/helium, 2800 hr~(-1), and 600-900℃, the catalytic activity of NO decomposition followed the order of NdSrCuO_(3.702)> NdSrCu_(0.8)Co_(0.2)O_(3.736) > NdSrCu_(0.6)Co_(0.4)O_(3.789) > Sm_(1.8)Ce_(0.2)Cu_(0.6)Co_(0.4)O_(4.187)> Sm_(1.8)Ce_(0.2)Cu_(0.8)Co_(0.2)O_(4.104)> Sm_(1.8)Ce_(0.2)CuO_(4.045), in concord with the sequence of decreasing oxygen vacancy or oxygen excess density. Based on the results, we concluded that the higher oxygen vacancy density and the stronger Cu~(3+)/Cu~(2+) redox ability of NdSrCu_(1-x)Co_xO_(4-δ) account for the easier activation of NO and consequently improve the catalytic activity of NO decomposition over the catalysts.  相似文献   
53.
以渍法制备了Pd/Ce0 ZrO4 /γ Al2 O3三效催化剂。在不同空速下 ,分别考察了空速对催化剂T30 % 、T50 % 、T90 % 的影响规律。详细分析了不同空速对催化剂起燃特性产生不同影响的原因所在。Pd/CeZrO4 /γ Al2 O3催化剂具有很好的起燃能力及空速特性。  相似文献   
54.
净化汽车尾气的三效催化剂   总被引:3,自引:0,他引:3  
王道  孟声 《环境导报》1999,(3):19-21
在我国,汽车尾气对大气的污染日趋严重,使用三效催化剂净化汽车尾气势在必行。介绍了几种主要的三效催化剂及其应用情况。  相似文献   
55.
The interactions between metals and oxide supports, so-called metal-support interactions (MSI), are of great importance in heterogeneous catalysis. Pd-based automotive exhaust control catalysts, especially Pd-based three-way catalysts (TWCs), have received considerable research attention owing to its prominent oxidation activity of HCs/CO, as well as excellent thermal stability. For Pd-based TWCs, the dispersion, chemical state and thermal stability of Pd species, which are crucial to the catalytic performance, are closely associated with interactions between metal nanoparticles and their supporting matrix. Progress on the research about MSI and utilization of MSI in advanced Pd-based three-way catalysts are reviewed here. Along with the development of advanced synthesis approaches and engine control technology, the study on MSI would play a notable role in further development of catalysts for automobile exhaust control.  相似文献   
56.
石油化工和化纤工业中大量使用钴,锰催化剂,应及时从各种废液中回收、再生,本文在25±1℃下研究了D_2EHPA-煤油从硫酸盐介质中萃取分离钴(Ⅱ)、锰(Ⅱ)的工艺,考察了萃取剂浓度、平衡pH值、相比对萃取的影响,求取了较适宜的工艺条件,利用五级逆流萃取模拟试验将钴、锰浓度比从1:1.5提高到1000:1,加入洗涤段后,又可获得金属含量比为1000的纯锰溶液,初步探索了用先进的液膜萃取新技术从溶液中分别富集、分离钴(Ⅱ)、锰(Ⅱ)的方法,找出了体系pH值对液膜萃取的影响,提出了从PTA氧化母液中回收废催化剂,萃取分离钴、锰,再生制备醋酸钴、醋酸锰和其他含钴、锰精细化工产品的工艺。  相似文献   
57.
采用等体积浸渍法制备了一系列不同Zr含量的ZrO2-Al2O3复合载体和Pd/ZrO2-Al2O3催化剂,利用连续流动微反装置考察了Pd/ZrO2-Al2O3催化剂的噻吩加氢脱硫(HDS)性能,并运用程序升温还原(TPR),程序升温脱附(H2-TPD,NH3-TPD)和N2物理吸附等技术对载体及催化剂进行了表征.结果表明:ZrO2-Al2O3复合载体中Zr含量对Pd基催化剂的HDS性能有较大影响,加入适量Zr可增大Pd/Al2O3催化剂的分散度及H2吸附量和酸量,减弱活性组分与载体的相互作用,使活性中心和噻吩吸附位增多以及活化能降低,从而有利于Pd基催化剂HDS反应活性的提高,w(Zr)为9%时Pd/ZrO2-Al2O3催化剂的活性最好.  相似文献   
58.
负载TiO2的泡沫镍网光催化降解甲醛的膜厚优化   总被引:1,自引:0,他引:1       下载免费PDF全文
采用负载TiO2的泡沫镍网光催化降解甲醛,考虑内部和外部质量传递,建立了可预测优化催化剂膜厚的数学模型.分析了TiO2膜厚对光催化降解甲醛的影响,并在模型基础上分析了催化剂层内光的衰减系数和污染物的有效扩散系数对最优催化剂膜厚的影响.结果表明,随着催化剂膜厚的增加,甲醛的降解先增加而后趋于平缓;最优催化剂膜厚受UV光衰减系数的影响较大,受污染物的有效扩散系数的影响较小;由于TiO2催化剂对254nmUV光的强烈吸收,优化的催化剂膜厚只有80nm左右.该模型对实验数据拟合较好.  相似文献   
59.
Antibiotic production wastewater usually contains high concentrations of antibiotic residues, which can cause instability and deterioration of biological wastewater treatment units and also domestication and proliferation of antibiotic-resistance bacteria. An effective pretreatment on antibiotics production wastewater is expected to selectively reduce the concentration of antibiotics and decrease the toxicity, rather than mitigate organic and other contaminants before further treatments. In this work, two polymer-based solid acids, PS-S and CPS-S bearing high concentrations of -SOH3 groups (up to 4.57 mmol/g), were prepared and successfully used for hydrolytic mitigation of 100 mg/L tylosin within 20 min. The co-existence of high concentrations of COD and humic substances did not affect the mitigation of tylosin obviously, while more than 500 mg/L of nitrogenous compounds suppressed the hydrolytic efficiency. Recycle and reuse experiments showed that the solid acids performed well in five cycles after regeneration. Three transformation products (P1, P2 and P3) were identified using UPLC-QTOF-MS/MS. Sugar moieties including mycarse, mycaminose, and mycinose detached and released simultaneously or in order from the 16-member lactone ring through desugarization, which led to a dramatic decrease in antibacterial activity as revealed by cytotoxicity evaluations using S. aureus. Ecotoxicity estimation indicated the acute toxicities of the hydrolyzed products to model species (e.g., fish, daphnid and green algae) were classified as “not harmful”. This work suggested an effective and selective method to pretreat tylosin-contained production wastewater by using polymer-based solid acids. These results will shed light on effective elimination of antibiotics pollution from pharmaceutical industries through strengthening the pretreatments.  相似文献   
60.
采用水热法制备了4种不同摩尔比的Cu-Mn-Ti/GS复合物催化剂,利用固定式反应床评价了其对二甲苯的催化氧化性能,并对催化剂进行了BET、XRD、SEM、TEM、XPS等表征,探讨了其对二甲苯的降解动力学.结果表明,当催化剂的Cu、Mn含量增加时,其比表面积有所降低,总孔容也降低,降解活性减小.催化剂中Cu-Mn呈现Cu_(1.5)Mn_(1.5)O_4和CuMn_2O_4两种晶格,活性组分有Cu~+、CuMn O和TiO_2.石墨烯载体的稳定性较好,Ti-Cu-Mn/GS(1∶1∶1)催化剂的颗粒分布较均匀,粒径也较小,降解二甲苯的T50为97℃,表现出较好的低温催化降解性能.催化剂对二甲苯的催化氧化降解过程符合一级反应动力学方程.  相似文献   
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