La0.7Sr0.3Mn1-xCoxO3-δ催化剂降低天然气发动机尾气排放的研究

采用喷雾热分解法制备了钙钛矿型催化剂La0.7Sr0.3Mn1-xCoxO3-δ(x=0、0.3、0.5、0.7),利用X射线衍射(XRD)和扫描电子显微镜(SEM)对催化剂进行了表征,在微型固定床反应器上优化了催化剂的B位掺杂Co.在天然气发动机排放试验台架上进行了空燃比特性、CH4排放和发动机尾气排放达标等测试试验.结果表明:在La0.7Sr0.3Mn1-x Co x O3-δ中掺杂适宜量的Co有助于提高催化剂的催化燃烧活性,改善催化剂比表面积和孔容积.当Co掺杂量为0.5时,所形成的La0.7Sr0.3Mn0.5Co0.5O3-δ催化剂对天然气发动机尾气排放物呈现出良好低温催化燃烧活性,对甲烷催化燃烧的起燃温度(T10)、半转化温度(T50)和完全转化温度(T90)分别为175、350和400℃,CO、NO x、非甲烷碳氢化合物(NMHC)和CH4的最大比排放量分别为3.01、1.72、0.31和0.85 g·kW-1·h-1,达到了国Ⅴ排放法规对天然气发动机有害排放物的限值要求,表明了La0.7Sr0.3Mn0.5Co0.5O3-δ适宜用于天然气发动机尾气低温催化燃烧的催化剂.     

Sulfur evolution in chemical looping combustion of coal with MnFe2O4 oxygen carrier

Chemical looping combustion （CLC） of coal has gained increasing attention as a novel combustion technology for its advantages in CO2 capture. Sulfur evolution from coal causes great harm from either the CLC operational or environmental perspective. In this research, a combined MnFe2O4 oxygen carrier （OC） was synthesized and its reaction with a typical Chinese high sulfur coal, Liuzhi （LZ） bituminous coal, was performed in a thermogravimetric analyzer （TGA）-Fourier transform infrared （FT-IR） spectrometer. Evolution of sulfur species during reaction of LZ coal with MnFeaO40C was systematically investigated through experimental means combined with thermodynamic simulation. TGA-FTIR analysis of the LZ reaction with MnFe2O4 indicated MnFe2O4 exhibited the desired superior reactivity compared to the single reference oxides Mn304 or Fe203, and SO2 produced was mainly related to oxidization of H2S by MnFe2O4. Experimental analysis of the LZ coal reaction with MnFe2O4, including X-ray diffraction and X-ray photoelectron spectroscopy analysis, verified that the main reduced counterparts of MnFe2O4 were Fe304 and MnO, in good agreement with the related thermodynamic simulation. The obtained MnO was beneficial to stabilize the reduced MnFe2O4 and avoid serious sintering, although the oxygen in MnO was not fully utilized. Meanwhile, most sulfur present in LZ coal was converted to solid MnS during LZ reaction with MnFe2O4, which was further oxidized to MnSO4. Finally, the formation of both MnS and such manganese silicates as Mn2SiO4 and MnSiO3 should be addressed to ensure the full regeneration of the reduced MnFe2O4.     

Effect of CaO on retention of S, Cl, Br, As, Mn, V, Cr, Ni, Cu, Zn, W and Pb in bottom ashes from fluidized-bed coal combustion power station

This work was conducted to evaluate whether Ca-bearing additives used during coal combustion can also help with the retention of some other elements. This work was focused on the evaluation of bottom ashes collected during four full-scale combustion tests at an operating thermal fluidized-bed power station. Bottom ashes were preferred to fly ashes for the study to avoid interference from condensation processes usually occurring in the post-combustion zone. This work focused on the behaviors of S, Cl, Br, As, Mn, V, Cr, Ni, Cu,Zn, W, and Pb. Strong positive correlations with CaO content in bottom ashes were observed（for all four combustion tests） for S, As, Cl and Br（R = 0.917-0.999）. Strong inverse proportionality was calculated between the contents of Pb, Zn, Ni, Cr and Mn and CaO, so these elements showed association to materials other than Ca-bearing compounds（e.g., to aluminosilicates, organic matter, etc.）. Somewhat unclear behaviors were observed for W, Cu, and V. Their correlation coefficients were evaluated as statistically ＂not significant＂, i.e., these elements were not thought to be significantly associated with CaO. It was also discovered that major enrichment of CaO in the finest bottom ash fractions could be advantageously used for simple separation of elements strongly associated with these fractions, mainly S and As, but also Cl or Br. Removal of5% of the finest ash particles brings about a decrease in As concentration down to 77%-80% of its original bulk ash content, which can be conveniently used e.g., when high As content complicates further ash utilization.     

燃煤锅炉一体化脱硫脱硝新方法应用

提出了一种燃煤锅炉一体化脱硫脱硝新方法。并在220D/H火电锅炉上进行了示范应用研究,通过检测烟气SO2和NOx变化情况,发现了该方法脱硫脱硝相互影响规律,认为燃煤锅炉一体化脱硫脱硝可行。     

防治煤矿火灾的凝胶泡沫材料制备及其性能研究*

为解决纯水玻璃（WG）凝胶泡沫强度低、泡沫稳定性差易破碎,凝胶固水性差等问题。将保水剂和成膜剂引入WG凝胶泡沫中,对水玻璃凝胶泡沫进行优化设计,最终制备出保水性高、泡沫稳定性高、成膜性好的WG凝胶泡沫。研究结果表明:WG凝胶泡沫材料的最佳复配体系是发泡剂为十二烷基醇醚硫酸酯钠（AES）和十二烷基硫酸钠(SDS)按1∶2比例复配,浓度为0.8%,胶凝剂WG浓度为8%,交联剂NaHCO3浓度为2%,聚丙烯酰胺浓度为0.4%,成膜剂A浓度为1%,保水剂B浓度为0.3%;改性后WG凝胶泡沫具有更加紧密的网状结构,稳定性好,并且具有较好的成膜性,常温下半衰期达40 d;阻化实验表明,100 ℃此凝胶泡沫阻化率高达78.35%,能有效减缓煤的氧化放热速率抑制自燃;煤堆燃烧实验表明,改性后WG凝胶泡沫能有效抑制煤的燃烧,防止煤复燃。     

基于热爆炸理论的煤燃点确定及动力学分析

为准确判断煤燃点,提高煤自燃灾害防治能力,依据热爆炸理论,结合煤自燃过程放热曲线,将煤自燃升温过程中微分热流曲线上第1处极小值点作为煤的燃点,计算煤着火前后放热过程动力学参数变化.结果表明:随升温速率增加,煤自燃反应放热过程逐渐向高温区域移动,煤燃点逐渐增大,反应的活化能逐渐减小;同一升温速率下燃点之后煤的活化能增大;...     

棉花阴燃和明火燃烧特性的对比研究

利用锥形量热仪,选取不同辐射强度,分别在使用和不使用点火器条件下,对棉花进行了热辐射引燃实验,发现在热辐射强度大于6kW/m2的情况下,使用点火器时棉花发生明火燃烧,不使用点火器时棉花发生阴燃燃烧。实验分别测得了在两种燃烧形式下的引燃时间、热释放速率、质量损失速率一氧化碳生成率,结果表明:无论是发生阴燃还是明火燃烧,引燃时间均随着辐射强度的增加而减小,且引燃时间平方根的倒数与辐射强度成线性关系;热释放速率、质量损失速率的峰值和平均值均随辐射强度的增加而增加,但在同一辐射强度下,明火燃烧的峰值和均值均比阴燃燃烧时的大;明火燃烧的一氧化碳平均生成率随着辐射强度的增加而减小,阴燃燃烧的一氧化碳平均生成率随着辐射强度的增加而增加。     

A Novel Solar Thermal Cycle with Chemical Looping Combustion

In this paper, we have proposed a thermal cycle with the integration of chemical-looping combustion and solar thermal energy with the temperature of about 500-600°C. Chemical-looping combustion may be carried out in two successive reactions between a reduction of hydrocarbon fuel with metal oxides and a reduced metal with oxygen in the air. This loop of chemical reactions is substituted for conventional combustion of fuel. Methane as a fuel and nickel oxides as an oxygen carrier were employed in this cycle. Collected high-temperature solar thermal energy is provided for the endothermic reduction reaction. The feature of the proposed cycle is investigated through Energy-Utilization Diagram methodology. As a result, at the turbine inlet temperature of 1200°C, the exergy efficiency of the proposed cycle would be expected to be about 4 percentage points higher than that of a conventional gas turbine combined cycle. Compared to the previous study of chemical-looping combustion energy systems, the proposed cycle with the integration of green energy and traditional hydrocarbon fuels will offer the possibility of both greenhouse gas mitigation, with green energy, and a new approach to the efficient use of solar energy.     

焦化备煤系统粉尘性质及燃爆可能性研究

为研究备煤系统工段过程的安全性,从某焦化厂备煤系统的粉碎机和输煤皮带处除尘管取部分除尘粉样进行工业分析和粒度分析,结果发现粉碎机处除尘粉水分较高,超过6%,输煤皮带除尘粉水分较低,不到3%。两者的粉尘粒度分布较为接近,主要粉尘粒径在2μm以内。配合煤水分到6%能产生一定量的粉尘,低于配合煤月平均水分和月最低水分,且现有个工段的扬尘质量浓度最高值仅30 mg/m~3,远低于煤粉爆炸下限浓度,具有较高的安全性。     

Direction of pressure wave propagation during combustion-induced rapid phase transition

In the work presented in this paper, the propagation direction of the pressure waves generated during combustion-induced Rapid Phase Transition (cRPT) was investigated. To this end, explosion tests were performed for CH₄/O₂/N₂/CO₂ mixtures in a tubular reactor. Ignition was provided at the top or at the bottom of the vessel. Pressure time histories were recorded by two transducers positioned one at the top and the other one at the bottom.Results have shown that the preferential direction for the pressure waves is that of the flame propagation. When the cRPT phenomenon is weak, an over-adiabatic pressure peak (of around 10–20 bar) can be measured by only one transducer and, in particular, by the transducer far away from the ignition point. Conversely, when the cRPT phenomenon becomes severe, over-adiabatic peaks (as high as 250 bar) can be detected even by the other transducer. Such peaks are the result of separate cRPT events that occur very close to the transducers and, thus, are not damped along the vessel length. In spite of the fact that the upward flame propagation is faster, the cRPT phenomenon is more severe in the case of downward flame propagation.