Catalytic combustion of methane over a highly active and stable NiO/CeO2 catalyst

In the last decades, many reports dealing with technology for the catalytic combustion of methane (CH₄) have been published. Recently, attention has increasingly focused on the synthesis and catalytic activity of nickel oxides. In this paper, a NiO/CeO₂ catalyst with high catalytic performance in methane combustion was synthesized via a facile impregnation method, and its catalytic activity, stability, and water-resistance during CH₄ combustion were investigated. X-ray diffraction, low-temperature N₂ adsorption, thermogravimetric analysis, Fourier transform infrared spectroscopy, hydrogen temperature programmed reduction, methane temperature programmed surface reaction, Raman spectroscopy, electron paramagnetic resonance, and transmission electron microscope characterization of the catalyst were conducted to determine the origin of its high catalytic activity and stability in detail. The incorporation of NiO was found to enhance the concentration of oxygen vacancies, as well as the activity and amount of surface oxygen. As a result, the mobility of bulk oxygen in CeO₂ was increased. The presence of CeO₂ prevented the aggregation of NiO, enhanced reduction by NiO, and provided more oxygen species for the combustion of CH₄. The results of a kinetics study indicated that the reaction order was about 1.07 for CH₄ and about 0.10 for O₂ over the NiO/CeO₂ catalyst.     

Flame Front Deformation Instabilities of Filtration Combustion for Initial Thermal Perturbation

The flame front deformation instability of low-velocity filtration combustion within an inert packed bed is studied based on the initial preheating non-uniformity. Based on the experimental phenomena, an initial thermal perturbation model is numerically proposed so as to predict the deformation behaviors of the flame front instabilities. The numerical prediction indicates that the assumption of an initial thermal perturbation is a feasible explanation as the cause of the flame front inclination instability. As the initial thermal perturbation increases, the phenomena of the flame front break and shrinking instabilities could easily occur at high filtration velocity or low equivalence ratio. Moreover, the evolutions of the flame front break rate and the shrinking rate are quantitatively analyzed.     

珲春地区高瓦斯矿井煤自然发火标志气体研究

为了探究珲春地区高瓦斯矿井煤自然发火情况，选取该地区板石煤矿22、23a和八连城煤矿18#、26#共4个煤层进行程序升温特性实验，分析了CO及烃类气体产生量随温度的变化规律，优选自然发火标志气体，测算煤自燃临界温度。结果表明，板石22、23a和八连城18#、26#四个煤层的自燃临界温度分别为101.0℃、97.6℃、121.0℃、169.1℃。CO和C2H4的初现温度大约在30℃与80～120℃，且产生量随温度单调递增，可作为煤自燃预测预报的主要参考指标|而同时，为了保证检测的全面与准确，还可以将规律性良好的其他烃类气体、烯烷比和链烷比进行辅助参考。     

Deposition of nanostructured LSM perovskite thin film on dense YSZ substrate by airbrushed solution combustion (ASC) for application in SOFC cathodes

To make SOFC high efficiency energy generation devices, thin ceramic films are proposed as their main components. The rate of the oxygen reduction reaction is relevant for the overall performance of the SOFC, hence a lot of attention is given to the cathodes and their interfaces. The airbrushed solution combustion (ASC) method was used to fabricate an LSM thin film on a dense YSZ substrate. A single phase LSM perovskite was obtained with very thin and interconnected porosity, and a small average grain size (55 nm). The nanostructured LSM thin film electrode showed a low total activation energy (1.27 eV) at high temperatures, but a high area specific resistance at 850°C (55 Ω.cm²). The activation energy for the dissociative adsorption and diffusion of oxygen was significantly low (1.27 eV), while the charge transfer and oxygen ion migration activation energy at the LSM/YSZ interface (1.28 eV) was closer to those usually reported.     

Concept design of a novel reformer producing hydrogen for internal combustion engines using fuel decomposition method: Performance evaluation of coated monolith suitable for on-board applications

Hydrogen addition effectively reduces the fuel consumption of spark ignition engines. We propose a new on-board reformer that produces hydrogen at high concentrations and enables multi-mode operations. For the proposed reformer, we employ a catalytic fuel decomposition reaction via a commercial NiO–CaAl₂O₄ catalyst. We explore the physical and chemical aspects of the reforming process using a fixed bed micro-reactor operating at temperatures of 550–700 °C. During reduction, methane is decomposed to form hydrogen and carbon. Carbon formation is critical to hydrogen production, and free space for carbon growth is essential at low temperatures (≤600 °C). We define a new accumulated conversion ratio that quantitatively measures highly transient catalytic decomposition. The free space of the coated monolith clearly aided low-temperature decomposition with negligible pressure drop. The coated substrate is therefore suitable for on-board applications considering that our reformer concept also utilizes the catalytic fuel decomposition reaction.     

近距离煤层群采空区漏风规律及防控措施研究

贵州地区煤层赋存条件复杂,煤层间距小,相邻采空区存在漏风通道的问题。采用SF6示踪法及重点区域指标气体数据分析法,对发耳煤矿采空区漏风规律及其治理措施进行研究。分析结果表明,由于相邻密闭效果欠佳,导致31004开切眼联络巷及31004工作面回风巷密闭漏风严重。31004采空区漏风通道主要是31004开切眼联络巷密闭及10^#煤层开采过程中对上部7^#煤层采空区造成二次扰动形成的纵向漏风通道;漏风量为83 m^3/min,采空区风速约为0.17 m/s。对存在的煤自燃隐患采取了注水降温措施,CO体积分数显著下降至(5~9)×10^-6。为即将开采的50105、50107工作面的煤自燃防控提供了科学依据和管控措施方案。     

水热法制备Sr_2FeNiO_6催化剂及其催化性能研究

采用水热法制备双钙钛矿催化剂Sr_2FeNiO_6,考察不同浓度KOH溶液(4 mol·L~(-1)、6 mol·L~(-1)、8 mol·L~(-1)、10 mol·L~(-1)、12 mol·L~(-1)、14 mol·L~(-1))对催化剂性能的影响,利用X射线衍射、比表面积测定、程序升温还原和扫描电镜等对样品进行性能表征,并以催化甲烷燃烧为目标,考察催化剂催化性能。结果表明,矿化剂KOH浓度对样品性能影响较大,当浓度为10 mol·L~(-1)时,起燃温度最低,T_(10%)为430℃;浓度为8 mol·L~(-1)时,样品比表面积最大,为19.0 m~2·g~(-1),完全燃烧温度最低,T_(90%)为610℃。     

采用绝热式自燃测试方法分析煤的自燃倾向

对煤的自燃倾向进行快速有效鉴别,有助于对煤的自燃倾向采取分级分类管理从而有效防治煤矿火灾,因而采用绝热式自燃测试方法对煤的自燃倾向进行准确分析很有必要。简要介绍绝热式自燃测试方法的测试原理及其仪器结构,模拟煤炭自燃的物理过程,通过采用包括反应器、气体预热铜管和跟踪温度控制方式等综合绝热措施以实现300 g煤样的自然发火实验,记录煤样从40℃上升到70℃的升温速率(或前30 h的升温速率),测试煤样的自燃特性曲线并分析曲线特征。即建立煤绝热氧化产热速率计算模型,结合实验数据计算所得的煤在绝热氧化条件下的升温速率和产热速率可鉴定煤自燃倾向性的强弱。采用绝热式自燃测试方法对不同煤的自燃倾向分析后表明,无烟煤和部分烟煤的自燃倾向较低,褐煤的自燃倾向较高,故而在煤矿开采时需特别注意褐煤的自燃倾向。     

Structural,microstructural, and magnetic studies of Y3Fe5-xNixO12 garnet nanoparticles

This paper reports the structural and magnetic properties of a series of Y₃Fe_5-xNi_xO₁₂ (x = 0, 0.05, 0.1, and 0.2) nanopowders synthesized by the citrate combustion method. We have discussed the change in different properties with the variation in calcination temperatures as well as the Ni ion substitution in yttrium iron garnet. X-ray diffraction study confirmed the desired garnet phase formation in all the calcined powders, and the crystallinity improved with an increase in calcination temperature. The crystallite sizes were observed in the range 47–52 nm and 84–94 nm for the samples calcined at 800 and 1000 °C, respectively. Scanning electron micrographs confirmed that the grains were in the nanometre range (132–170 nm) at 800 °C and increased (351–363 nm) at 1000 °C. Larger grains at high calcination temperature resulted in the enhanced saturation magnetization and a decrease in coercivity. Curie temperature (T_c) was observed in the range 558–560 K for all the calcined Y₃Fe_5-xNi_xO₁₂ samples. Nickel substitution for iron sites in Y₃Fe_5-xNi_xO₁₂ decreased the saturation magnetization and enhanced the coercivity. This could be related to the substitution of Ni ions for tetrahedral iron sites, which changed the magnetic exchange interactions of different lattice sites. The magnetic anisotropy constant (K) increases with the enhancement of calcination temperature, whereas it decreases with nickel ion substitution in Y₃Fe_5-xNi_xO₁₂. This study suggests that the structural and magnetic properties can be tuned by Ni substitution for the Fe ions in Y₃Fe₅O₁₂ garnets at different calcination temperatures, which make them promising candidates for various technological applications.     

两池火耦合作用下柴油拱顶罐热响应的数值模拟

化工园区多池火事故是典型的高后果低概率事件。鉴于目前两池火辐射模型存在一定局限性，本文采用数值模拟方法，以3个直线排布的5000m³柴油拱顶罐为研究场景，从热释放速率、火焰形态、热辐射强度三方面分析两池火燃烧特性，并与单池火场景对比，考虑储罐间距这一影响因素，进一步研究目标储罐热响应。结果表明：采用GB 50160—2008（2018年版）规定的防火间距，两燃烧罐产生的池火会发生耦合作用，并得出目标储罐受到的热辐射强度分布，最高热辐射达17.04kW/m²；两池火作用下目标储罐的温度、Mises应力与失效时间分别为644℃、356MPa、936s，单池火为488℃、280MPa、2880s，目标储罐在两池火作用下的变形也比单池火更为严重；随着储罐间距增加，目标储罐的温度与Mises应力逐渐减小，失效时间逐渐增加，当储罐间距为标准防火间距的2.5倍（20m）时，失效时间为2800s，与单池火作用产生的失效时间2880s较为接近。本研究可为优化储罐防火间距及区域韧性提升提供理论指导。