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.     

故障安全控制系统在催化裂化装置的应用

介绍霍尼韦尔公司故障安全控制系统FSC的技术特点以及在我厂重油催化裂化装置的应用情况，说明了该装置故障安全控制系统组成和操作界面，并总结了应用效果。     

用MnSO4-Ce(SO4)2协同催化快速测定COD的研究

本文探讨了以MnSO4-Ce(SO4)2复合催化剂代替标准重铬酸钾法中的Ag2SO4，用密封消解法测定废水COD值的可行性，研究了复合催化剂总量、配比、消解时间、溶液酸度等因素对COD测定的影响。通过对各种废水COD值的测定表明，用MnSO4-Ce(SO4)2做催化剂，在165℃，较低酸度，密封消解15min是可行的。     

用于燃料电池的甲醇水蒸气重整反应制氢的研究

研究了甲醇水蒸气重整制氢反应过程中各种因素对Cu／ZnO／Al2O3催化剂的活性和选择性的影响。结果表明：Cu／Zn比为2．0的催化剂在250℃反应时，催化剂效果较好，最合适反应条件是：压力0．1MPa，温度250℃，n(H2O)：n(CH3OH)=1．0-1．2，液体流速0．1mL／min。在Cu／ZnO／Al2O3)，催化剂上，甲醇水蒸气重整、甲醇分解和水气转换反应随反应条件的不同而发生相互抑制或促进作用。     

改性催化裂化废催化剂吸附水中氨氮的研究

考察了振荡时期温度、ＰＨ吸附效果的影响，通过吸附热力学实验，探讨了吸附机理，结果表明，温度是影响吸附效果的主要因素；等温吸附规律可用Ｆｒｅｕｎｄｌｉｃｈ模式和Ｌａｎｇｍｕｉｒ模式较好地描述；可能的吸附机理为：一是ＮＨ分子通过偶极力和氢键方面吸附，二是ＮＨ４通过离子交换面吸附。     

利用XPS研究复合氧化物催化剂在汽车尾气净化中硫中毒及抗硫中毒机理

运用ＸＰＳ分析方法研究一系列复合氧化物催化剂中毒前后硫在其表面的各种形态及催化剂活性组分中毒前后的组成，价态，化学机理及其变化。结果表明，ＳＯ２在催化剂活性中心进行化学吸附，然后一部分ＳＯ２与活性组分生成相应的亚硫酸盐和硫酸盐，从而使催化剂失活。     

An assessment of how distance and diesel oxidation catalyst will impact thermal decomposition behaviors of particles

Decomposition mass loss and pyrolysis products analyses of particles sampled at various locations along the tailpipe of a Euro-IV diesel engine were performed using a thermogravimetry in conjunction with Fourier transformation infrared spectrometry-mass spectrum. Diesel particles were collected at the same location with and without diesel oxidation catalyst (DOC) mounted on the test engine separately. The three poles in thermal gravity-differential thermal gravity images suggested that the decomposition process of diesel particles could be divided into three stages which correspond to the decompositions of lower boiling substances, higher boiling substances and soot respectively. It is noticed that no matter whether DOC was mounted or not, the further the particles were sampled away from the engine block, the lower the peak temperatures and the heavier the mass losses within the first two stages, which indicated that the soluble organic fraction in the particle samples increased and therefore lowering the activation energy of thermal decomposition. Hydroxyl, ammonia, C_xH_y fragments, benzene, toluene, and phenol were found to be the primary products of particle decomposition, which didn't change with the location of particle sample point. The employment of DOC increased the activation energy for particle oxidation and resulted in a higher peak temperature and lower mass loss within the first-stage. Moreover, the CO stretching bands of aldehyde and ketone at 1771 cm^?1 was only detected without a DOC, while the NO₂ peak at 1634 cm^?1 was solely noticed with the presence of DOC. Compared to the first-stage pyrolysis products, more polycyclic aromatic hydrocarbons and less C_xH_y fragments were seen in the second-stage.     

超临界水氧化技术处理有机废水的研究

超临界水是处理难氧化有机污染物的一种很好媒介,因为在超临界状态下有机污染物和氧化剂能够互溶而加快反应速度,具有去除率高,反应时间短且无污染等特点,因而受到了越来越多的关注。本文主要概述了超临界水氧化的特点、机理、工艺流程和存在的问题,介绍了当前超临界水氧化处理难降解污染物的效果、动力学、催化剂研究等情况,并展望了其应用前景。     

用MnSO_4作催化剂开管测定废水COD

本研究介绍了用硫酸锰代替硫酸银作催化剂快速开管测定废水中COD的方法。该方法降低了分析成本 ,且使样品的回流时间缩短到 12min ,而准确度和精密度同标准法基本相同。此法取样量少 ,消解速率快 ,适用于大批量水样的测定。     

电石渣和铝土粉的高温燃烧脱硫特性及微观分析

研究了电石渣和铝土粉作为燃煤添加剂的高温脱硫特性及其微观反应机理，发现在1200℃下燃煤中同时添加电石渣和铝土粉时，低温硫析出峰与只添加电石渣时几乎一致，而高温硫析出峰则大大降低，从而使脱硫率由30．5％明显提高到45．19％．XRD和SEM分析表明：电石渣中富含的CaO以及铝土粉中富含的Al2O3，与燃煤固硫过程中生成的部分CaSO4在高温下反应生成了耐热物相“硫铝酸钙”，是钙铝基添加剂比单纯钙基具有更高脱硫率的最主要原因．另外铝土粉增强了电石渣燃煤固硫渣的熔融程度，从而使硅酸盐熔融物有更多机会将CaSO4等固硫产物包裹以抑制其高温分解，是它具有更高脱硫率的另一个原因．