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1.
针对氢气添加的LPG(液化石油气)+空气预混火焰结构进行了数值研究, 详细计算了在含氢比a为0%到45%、稀释引子D为21%到16%条件下的自由蔓延火焰, 得到了不同燃烧条件(φ=0.7-1.4)下的绝热燃烧速率变化规律. 由于LPG中的主要成分为丙烷和丁烷, 作者针对C3和C4物质提出了详细化学反应动力学系统, 并针对氢气添加的丁烷燃烧过程进行了数值计算, 得到了与实验相一致的结果, 验证了改进的详细化学机理的有效性. 此外, 进一步计算了对撞双火焰的加氢LPG火焰, 更加深入地探讨了火焰拉伸对燃烧稳定性和温度的影响, 重点研究了φ在0.5到0.7的稀薄燃烧, 验证了氢气添加可以有效提高稀薄燃烧条件下熄火拉伸率, 扩大稀薄燃烧的极限, 增加火焰的稳定性. 相似文献
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通过对贫燃条件下(燃料与空气化学计量比φ=0.60-0.80)的甲烷/一氧化碳/空气火焰结构进行数值模拟,研究燃料中一氧化碳添加量对层流燃烧速度、氮氧化合物的排放以及熄火拉伸率的影响.随着燃料中一氧化碳添加量的不断增加,层流燃烧速度有所下降,这与燃料中加入氢气产生的现象有所不同.为了解释这一现象,本文深入探讨了层流燃烧速度与H+OH浓度峰值之间的关系,结果表明,一氧化碳的增加导致H+OH浓度峰值呈线性下降,与层流燃烧速度下降趋势完全一致.随着一氧化碳的增加,氮氧化合物排放量有所下降.探讨了NO的生成机理,且由敏感性分析得到生成NO的重要反应,分析当一氧化碳量增大时,NO的浓度以及重要反应的NO生成率均下降.此外,利用数值模拟求解径向拉伸率,深入分析燃料中添加一氧化碳时拉伸率对贫燃火焰稳定性的影响.由计算结果得到熄火拉伸率,发现燃料中一氧化碳的添加在一定程度上能够增强火焰的稳定性. 相似文献
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Summary The exhaust gas of a LPG fuelled engine is drawn through two bubblers in series in an ice bath, and filled with saturated 2,4-dinitrophenylhydrazine in 2M HCl. After heating the derivatives are extracted with toluene-cyclohexane and 1l samples injected on-column on a OV1 capillary column. Using an FID the lower limit of detection is 15–18 pg for formaldehyde (about 8–10 ppbv for a 16l exhaust sample). Taking the blank into account, the limit is about 40 ppbv.The exhaust gases of a LPG-fuelled engine contain formaldehyde, acetaldehyde, propionaldehyde, acrolein and acetone. Carbonyl compounds of more than 3 C-atoms were not found in detectable amounts. The engine was rund under stoichiometric, lean and rich air/fuel conditions. Under rich conditions the concentrations of the aldehydes were: formaldehyde 2.8 ppm, acetaldehyde 1.3 ppm, propionaldehyde 0.06 ppm, acrolein 0.03 ppm, acetone 0.17 ppm; under stoichiometric conditions: 4.5, 1.6, 0.10, 0.03 and 0.18 ppm respectively; under lean conditions 17.0, 2.9, 0.13, 0.07 and 0.27 ppm respectively. These figures demonstrate the necessity of measuring aldehydes in exhaust gases of LPG-fuelled engines. 相似文献
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《Arabian Journal of Chemistry》2023,16(2):104496
The aim of this study was to examine the propagation characteristics of liquified petroleum gas (LPG)/air explosion. As such, the flame propagation process and pressure parameters of LPG explosion with an equivalent ratio of 1 were obtained using horizontal, long straight pipes and a high-speed camera. The large eddy simulation and power-law flame model were used to reproduce the simulation results, and the morphological evolution of the flame front during the explosion process was analyzed. The results showed that as the blockage ratio gradient increased, the time required for the flame to propagate from the electrode to the end of the pipe increased. Meanwhile, a flocculent flame formed at the end of the pipeline with a blockage ratio of 91%. Additionally, the maximum flame propagation speed changed in the same way as the blockage ratio. The gradient change of the barrier blockage ratio considerably influenced the pressure kinetics characteristics of LPG explosion: the maximum explosion pressure increased first and then decreased, the time to reach the maximum explosion pressure increased, and the deflagration index increased first and then decreased. The chemical kinetics analysis of premixed gas showed that when propane, n-butane, and isobutane were present in the premixed system, some of the elemental reactions that promote n-butane consumption inhibited propane and isobutane consumption. Meanwhile, the formation and consumption rate of H*, O*, and OH* from LPG during the explosion process was less than that of single-component combustible gas except propane. 相似文献
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A simple sample enrichment technique, electrokinetic migration enrichment in single phase using a designed device, coupled with ion chromatography is presented for the determination of four anions (H(2)PO(4)(-), Cl(-), NO(3)(-), and SO(4)(2-)) in liquefied petroleum gas by liquid adsorption. The electrokinetic migration enrichment is based on the phenomenon of ion electrokinetic migration to the opposite electrode. When the anions migrated to the anode in a smaller volume chamber under the electric field, the concentration was realized. The main parameters affecting enrichment efficiency of applied voltage and enrichment time were investigated. The ion chromatography condition for anions separation was also studied. Under the optimal electrokinetic migration enrichment and ion chromatography conditions, the four anions were detected simultaneously with good linear relationship (r(2) = 0.9908-0.9968) and high precisions (less than 5% of the relative standard deviations of peak areas). The limits of detection of anions (S/N of 3) were in the range of 8-600 μg L(-1). The enrichment factors of the four anions ranged from 3.1 to 5.8. The established method was successfully applied to the analysis of the trace anions in liquefied petroleum gas by liquid adsorption with satisfactory results. The advantages of this method are simple operation and low cost. 相似文献
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针对乙炔/空气预混火焰中CO添加对炭黑生成的影响进行了详细的数值模拟.通过对含有不同CO添加量的火焰的模拟结果比较,研究CO添加的温度和化学作用对于炭黑形成的影响.计算结果显示CO添加使炭黑的生成单调下降.炭黑体积分数和成核速率随着温度的升高而增加,到达一个阈值后,再随温度的升高而减少.从炭黑生成的H-萃取角度来看,由于反应OH+CO=CO2+H的向右速率增加,H原子增加以及OH自由基减少,CO添加会激发炭黑生成.从炭黑生成的C-添加机理来看,CO添加减小了C2H2的消耗速率,CO添加也有助于炭黑生成,但CO添加降低了燃料中C2H2的体积分数,使得炭黑表面增长速率降低. 相似文献
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采用甲醇合成催化剂与脱水催化剂机械混合,制备了液化石油气(LPG)合成催化剂。以模拟生物质气为原料气,在固定床单管实验装置上,温度(220~330 ℃)、压力(1.2~5.1 MPa)和空速(500~3 000 h-1)条件下考察催化剂的性能。结果表明,在325 ℃、2.1 MPa、1 500 h-1条件下,CO转化率达到72.36%,LPG占烃类产物的71.21%。当设定温度为325 ℃、压力2.1 MPa时、空速≤2 500 h-1时,系统可以稳定运行;空速达到3 000 h-1时,反应器内部温度迅速升高无法控制,造成催化剂烧结失活。针对上述催化剂,采用NH3-TPD、XRD、N2吸附-脱附和TPO对催化剂进行了表征。结果表明,催化剂的积炭、强酸位酸性降低及比表面积的降低是导致催化剂活性降低的重要影响因素。 相似文献
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利用大口径毛细管气相色谱法测定液化气中的含硫化合物 总被引:5,自引:0,他引:5
利用大口径毛细管色谱柱、不分流进样、氢焰离子化检测器(FID)、双火焰光度检测器(DFPD),与气相色谱-质谱(GC-MS)联用技术相结合,对脱硫后的液化气进行测定,成功地鉴定出17种含硫化合物。该法简便、快速,对含硫化合物的检测灵敏度高。 相似文献
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采用共沉淀法制备Cu/ZnO催化剂、水热合成法制备H-β分子筛、通过物理包膜法制备了具有核壳结构的Cu/ZnO@H-β-P催化剂,并用于合成气制备液化石油气(LPG)反应。通过XRD、NH3-TPD、BET和SEM-EDS等手段对催化剂进行了表征,利用固定床连续反应装置对催化剂进行了活性评价。结果表明,Cu/ZnO@H-β-P催化剂是具有中孔的核壳结构材料,其协同作用打破了原有的热力学平衡,促进了甲醇→DME→LPG串联反应的连续进行。与物理混合的Mix-Cu/ZnO-H-β催化剂相比,Cu/ZnO@H-β-P催化剂的CO转化率和LPG选择性更高,空速和反应温度对催化剂活性影响明显,最佳空速和反应温度分别为2 400 h~(-1)和350℃。使用Cu/ZnO@H-β-P催化剂在最佳条件下进行合成气制备LPG反应,CO转化率达到了57.22%,LPG选择性达到了60.52%。 相似文献
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通过对正丁烷/氢气/空气混合物在Pt 催化表面的详细反应机理分析, 研究了氢气添加对正丁烷/空气混合物催化着火过程的影响. 研究发现, 在正丁烷/空气混合中添加氢气有助于正丁烷在更低的温度下实现催化着火, 而且不同的氢气添加量对混合物的着火温度和着火过程呈现不同的影响: 当氢气添加量较小时, 氢气的作用主要呈现为热影响; 而当氢气添加量较大时, 氢气的作用主要呈现为化学影响. 这些结果与实验结果是一致的. 本文进一步确定了发挥不同作用的氢气添加量的范围, 并分别对热作用和化学作用情况下的着火启动反应进行了动力学分析. 相似文献
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采用火焰原子吸收法监测空气与废气中气溶胶样品的铅尘和铅烟 ,依照有关部门已制订的一批统一 (或推荐 )的监测方法资料 ,通过自身一系列的方法适用性检验 ,经外场的采样效率试验直至实验室内的空白值、酸度及样品基体干扰影响和消除的尝试 ,加以改变仪器工作条件比对和回收试验等 ,使实测样品获得了满意结果。铅的方法检出限为 0 0 5 μg/mL/ 1 %吸收 ,测定下限为 0 1 5 μg/mL ,线性范围 0 5~ 1 0 0 μg/mL ,测定范围 :0 0 5~ 5 0mg/m3 ,当采样体积为 5 0m3 ,取 1 / 2张滤膜 (直径 8~ 1 0cm)进行铅尘测定时气溶胶中铅的最低检出浓度为 2× 1 0 - 4mg/m3 ,采样效率为 98% ,样品回收率为 92 3%。 相似文献
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《Analytical letters》2012,45(10):717-721
Abstract The sensitivity for selenium determination with atomic absorption spectrophotometry is enhanced to a large extent by introducing hydrogen selenide gas into an argon-hydrogen flame. As a reducing agent, zinc granular and stannous chloride is successfully used for quantitative and rapid productions of hydrogen selenide from selenium(IV) solution. The sensitivity for 1 % absorption of the signal is estimated to be about 0.02 ppm of selenium. 相似文献
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固相微萃取-脉冲火焰光度法测定大气及水中的路易氏剂 总被引:1,自引:0,他引:1
建立了固相微萃取(SPME)与气相色谱/脉冲火焰光度检测器(GC/PFPD)联用测定大气和水中路易氏剂及其水解产物的方法。探讨了影响SPME萃取效率的萃取头类型、萃取时间、解吸时间等因素。优化了PFPD的条件参数、衍生化试剂及衍生条件。在优化的条件下,路易氏剂衍生产物的响应值与浓度有良好的线性关系。本方法对水中路易氏剂及其水解产物的检出限为0.1μg/L;气体中路易氏剂的检出限为10ng/m^3;水样的加标回收率为96.7%-102.1%;气体样品的加标回收率为94.9%-103.0%;RSD为2.06%。 相似文献
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The effects (chemical, thermal, transport, and radiative) of CO2 added to the fuel side and oxidizer side on the flame temperature and the position of the flame front in a one-dimensional laminar counterflow diffusion flame of methane/N2/O2 were studied. Overall CO2 resulted in a decrease in flame temperature whether on the fuel side or on the oxidizer side, with the negative effect being more obvious on the latter side. The prominent effects of CO2 on the flame temperature were derived from its thermal properties on the fuel side and its radiative properties on the oxidizer side. The results also highlighted the differences in the four effects of CO2 on the position of the flame front on different sides. In addition, an analysis of OH and H radicals and the heat release rate of the main reactions illustrated how CO2 affects the flame temperature. 相似文献
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以实验室合成的氟代叔丁烷、氟代仲丁烷、氟代正丁烷为参考,建立了烷基化物料中C4氟代烃的气相色谱/氢火焰离子化检测(GC/FID)分析方法。提出了利用气相色谱/原子发射光谱(GC/AED)按元素响应的特点求算C4氟代烃在GC/FID上相对校正因子的方法。方法采用OV-225(50 m×0.25 mm i.d.×0.25 μm)和SE-54(44 m×0.22 mm i.d.×0.25 μm)串联柱为分析柱,FID为检测器,校正归一化或间接外标方法进行定量,具有重复性好、应用移植便利、操作简单等特点,对氟代叔 相似文献
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提高碘量法测定天然气中硫化氢效率的方法 总被引:1,自引:0,他引:1
碘量法是测定管道输送天然气中硫化氢的一种经典方法,而管道输送天然气中硫化氢含量较低,按照GB/T11060.1–2010方法测定,取样量较大,取样时间长,影响工作效率。针对此问题,从两方面对碘量法进行改进:减小天然气取样量进行试验,并与国标规定取样量时的实验结果进行比对,确定最佳取样量;增大取样流量进行试验,并与国标规定取样流量时的实验结果进行比对,确定最佳取样流量。对硫化氢质量浓度为7.2~14.3,14.3~28.7 mg/m~3的天然气样品进行试验测定,结果表明,将天然气取样量减少为20 L,取样时间分别由200,100 min缩短为40 min;将天然气取样流量设定为750 m L/min,取样时间分别由200,100 min缩短为133,67 min。减少取样量或者提高取样流量,均能缩短管输天然气的取样时间,提高检测效率。 相似文献
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Dr. Denis Bernsmeier Sören Selve Jörg Nissen Dr. Natalia Maticiuc Josefa Ibaceta-Jaña Prof. Bernd Szyszka Dr. Ruslan Muydinov 《Chemphyschem》2023,24(14):e202200650
A single step deposition technique of Pt/C films for electrocatalytic applications is presented. The hollow cathode gas flow sputtering (GFS) method allows a catalyst production within few minutes without further steps. The herein presented films consist of small Pt nanocrystals (2–5 nm) deposited in a matrix of nanocrystalline carbon. The films show a low and stable overpotential under acidic conditions in the hydrogen evolution reaction (HER). Relatively low Pt-mass activity (<1 mA/μgPt) is attributed to the yet too high Pt-content in the films. Another issue discovered in this work is a non-graphitic state of carbon resulting in its high resistivity. Still, the GFS deposition technique providing by nature high deposition rates and a substance-to-material yield of 80–90 % is advantageous than other sputtering techniques and especially chemical methods in that sense. This technique is scalable to areas in the range of square meters and thus represents an attractive way to efficiently produce large-scale cathode coatings for industrial electrolysers. 相似文献