Efficient degradation of organic pollutants by S-NaTaO3/biochar under visible light and the photocatalytic performance of a permonosulfate-based dual-effect catalytic system

Removing large concentrations of organic pollutants from water efficiently and quickly under visible light is essential to developing photocatalytic technology and improving solar energy efficiency. This study used a simple hydrothermal method to prepare a non-metallic, S-doped NaTaO₃ (S-NTO) photocatalyst, which was then loaded onto biochar (BC) to form a S-NTO/BC composite photocatalyst. After uniform loading onto BC, the S-NTO particles transformed from cubic to spherical. The photogenerated electron-hole pair recombination probability of the composite photocatalyst was significantly lower than those of the NTO particles. The light absorption range of the catalyst was effectively widened from 310 nm UV region to visible region. In addition, a dual-effect catalytic system was constructed by introducing peroxymonosulfate (PMS) into the environment of the pollution to be degraded. The Rhodamine B, Methyl Orange, Acid Orange 7, tetracycline, and ciprofloxacin degradation efficiency at 40 mg/L reached 99.6%, 99.2%, 84.5%, 67.1%, and 70.7%, respectively, after irradiation by a 40 W lamps for 90 min. The high-efficiency visible-light catalytic activity of the dual-effect catalytic system was attributed to doping with non-metallic sulfur and loading of catalysts onto BC. The development of this dual-effect catalytic system provides new ideas for quickly and efficiently solving the problem of high-concentration organic pollution in aqueous environments, rationally and fully utilizing solar energy, and expanding the application of photocatalytic technology to practice.     

柴油机排放碳颗粒物的催化燃烧

在热天平装置上考察了柴油机和碳颗粒物燃烧催化剂的活性，讨论了样品制备因素对样品失重的影响，这些因素包括碳颗粒物组成、催化剂栽体、催化剂与碳颗粒物质量比，着重筛选了催化剂的组份，得到了组份催化剂ＣｕＣｌ２－ＫＣｏ－ＮＨ４ＶＯ３其５５０℃焙烧后能使样品的Ｔｍ和Ｔｆ值都降低１８０℃以上，并对催化剂的热稳定性进行了研究。     

安太堡露天煤矿煤矸石自燃的治理

论迷了安太堡矿煤矸石自燃的原因、特征及治理措施,并对今后的工作提出了几点建议。     

常温空气无焰燃烧中NOx生成的研究

研究了常温空气无焰燃烧中Nox的生成规律.实验研究和计算分析表明,在燃烧器射流对称轴上(300mm×2000mm的空间内),自喷口至炉膛中心处,有一个温度较低的剧烈的燃气与空气扩散混合区,在此区域内,不生成Nox;温度大于1320K的区域,开始生成N2O;在炉膛后部温度大于1810K的高温区,开始生成NO.过量空气系数与容积热负荷对烟气中Nox生成量的影响不大与传统的扩散火焰或预混火焰不同,常温空气无焰燃烧反应发生在一个弥散的宽广区域,在整个炉膛内同时进行,炉膛内高温区面积很小,因而Nox的生成量低,排放稳定.     

气相连通罐组群罐燃爆风险定量评估技术研究

炼化企业气相连通罐组存在群罐重大火灾风险,需要采取系统评估、层层设防的思路进行防控。采用HALOPA技术,结合中国石化风险矩阵标准,建立基于风险的气相连通罐组重大燃爆风险控制准则、不同罐容的事故后果等级划分标准、各类保护措施的风险消减因子和燃爆事件可能性评估方法以及相关重要设计要求。案例分析表明,VOCs气相连通罐组群罐燃爆风险定量评估方法可对群罐火灾风险进行快速量化评估,可用于气相连通罐组的风险评估和工程安全设计。     

Component regulation in novel La-Co-O-C composite catalyst for boosted redox reactions and enhanced thermal stability in methane combustion

A novel La-Co-O-C (LC-C) composites were prepared via a facile co-hydrothermal route with oxides and glycerol and further optimized for methane catalytic activity and thermal stability via component regulation. It was demonstrated that Co₃O₄ phase was the main component in regulation. The combined results of X-ray photoelectron spectroscopy (XPS), temperature-programmed desorption of oxygen (O₂-TPD), temperature-programmed reduction of hydrogen (H₂-TPR), temperature-programmed desorption of ammonia/carbon dioxide (NH₃/CO₂-TPD) revealed that component regulation led to more oxygen vacancies and exposure of surface Co²⁺, lower surface basicity and optimized acidity, which were beneficial for adsorption of active oxygen species and activation of methane molecules, resulting in the excellent catalytic oxidation performance. Especially, the (3.5)LC-C (3.5 is Co-to-La molar ratio) showed the optimum activity and the T₅₀ and T₉₀ (the temperature at which the CH₄ conversion rate was 50% and 90%, respectively) were 318 and 367°C, respectively. Using theoretical calculations and in situ diffuse reflection infrared Fourier transform spectroscopy characterization, it was also found that the catalytic mechanism changes from the “Rideal-Eley” mechanism to the “Two-term” mechanism depending on the temperature windows in which the reaction takes place. Besides, the use of the “Flynn-Wall-Ozawa” model in thermoanalytical kinetics revealed that component regulation simultaneously optimized the decomposition activation energy, further expanding the application scope of carbon-containing composites.     

黄磷尾气的综合利用及净化途径探讨

对黄磷尾气综合利用的途径和生产的技术进行了探讨,应用变温吸附和变压吸附分离技术处理黄磷尾气,净化效果较好,再生容易,各种杂质脱除率高.     

Degradation of nitrobenzene in aqueous solution by ozone-ceramic honeycomb

IntroductionAs a promising advanced oxidation technology for watertreatment ,catalytic ozonation has received great attentionforthe efficient degradation of organic compoundsinrecent years(Legube , 1999) . Some studies showed that homogeneousand heterogen…     

不同DSA类阳极催化降解苯胺的试验研究

很多工业都产生苯胺废水。本文用新兴的电化学催化系统 ,采用特殊工艺自制的两种 DSA类电极作为阳极 ,对自配的苯胺溶液进行了降解处理 ,并得出了本试验范围内的最佳条件。     

Experimental and theoretical studies on NO selective catalytic oxidation over α-MnO2

Based on the experimental and theoretical methods, the NO selective catalytic oxidation process was proposed. The experimental results indicated that lattice oxygen was the active site for NO oxide over the $\mathrm{\alpha }$-MnO₂(110) surface. In the theoretical study, DFT (density functional theory) and periodic slab modeling were performed on an $\mathrm{\alpha }$-MnO₂(110) surface, and two possible NO oxidation mechanisms over the surface were proposed. The non-defect $\mathrm{\alpha }$-MnO₂(110) surface showed the highest stability, and the surface O_s (the second layer oxygen atoms) position was the most active and stable site. O₂ molecule enhanced the joint adsorption process of two NO molecules. The reaction process, including O₂ dissociation and O=N-O-O-N=O formation, was calculated to carry out the NO catalytic oxidation mechanism over $\mathrm{\alpha }$-MnO₂(110). The results showed that NO oxidation over the $\mathrm{\alpha }$-MnO₂(110) surface exhibited the greatest possibility following the route of O=N-O-O-N=O formation. Meanwhile, the formation of O=N-O-O-N=O was the rate-determining step.