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Contaminant Estimates and Removal in Product Gas from Biomass Steam Gasification

机译:生物质蒸汽气化过程中产物气中污染物的估算和去除

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摘要

Permanent gas species, tarcompounds, sulfur compounds, and ammonia produced from a bench-scale (~1 kg/h) fluidized-bed biomass gasifier were analyzed. Two commercial Ni-based catalysts and one commercial ZnO sorbent were evaluated under varied conditions by quantifying contaminants from the reactor inlet and outlet with specific sampling and analysis methods. The Ni catalysts targeted tar destruction and ammonia reduction, and the ZnO sorbent was selected for sulfur compound removal. Tar components were identified by gas chromatography-mass spectrometry (GC-MS) and quantified by GC-fiamc ionization detector (FID). A total of 13 compounds (≥C_6) were identified in raw product gas, principally "lighter tar" species with an average concentration of 15.5 g m~(-3) (dry gas basis). For tar species that were not detected by GC, a gravimetric method was used to quantify the portion of "heavier tar" (5.3 g m~(-3) dry gas basis). These data are raw gas tar concentrations for the gasifier-opcrating conditions used for the remainder of the tests. The performance of two commercial Ni catalysts were evaluated by comparing the concentrations of both "lighter tar" and "heavier tar" after the raw gas passed through the tar-reforming reactor. Concentrations of hydrogen sulfide (H_2S), carbonyl sulfide (COS), and thiophene (C_4H_4S) in the raw, dry, product gas averaged 93, 1.7, and 2.2 ppmv, respectively. C_4H_4S and two additional sulfur compounds, benzothiophenc and one unidentified compound (UN l), were found in the tar-trapping solution. Removal of sulfur compounds using the ZnO sorbent at varied temperatures and gas hourly space velocities (GHSVs) was investigated. The primary sulfur component, H_2S, was reduced to less than 1 ppmv; COS was not reduced significantly; and C_4H_4S concentrations were not affected at all. The average NO and ammonia concentrations were determined to be 8.2 and 2662 ppmv in the dry gas, respectively. Both were successfully converted to permanent gas species by Ni catalysts.
机译:分析了台式规模(〜1 kg / h)流化床生物质气化炉产生的永久性气体,焦油化合物,硫化合物和氨气。通过使用特定的采样和分析方法对来自反应器入口和出口的污染物进行定量分析,在不同条件下评估了两种商用Ni基催化剂和一种商用ZnO吸附剂。 Ni催化剂的目标是焦油的破坏和氨的减少,并且选择ZnO吸附剂来去除硫化合物。通过气相色谱-质谱(GC-MS)鉴定焦油成分,并通过GC-fiamc电离检测器(FID)定量。在原料气中总共鉴定出13种化合物(≥C_6),主要是“轻质焦油”,平均浓度为15.5 g m〜(-3)(基于干气)。对于GC未检测到的焦油种类,采用重量分析法定量“较重的焦油”(5.3 g m〜(-3)干燥气体基准)。这些数据是其余测试中气化炉-op化条件下的原煤气焦油浓度。通过比较原料气通过焦油重整反应器后“较轻的焦油”和“较重的焦油”的浓度来评估两种市售Ni催化剂的性能。原料气,干燥产物气中的硫化氢(H_2S),羰基硫(COS)和噻吩(C_4H_4S)的平均浓度分别为93、1.7和2.2 ppmv。在捕集焦油的溶液中发现了C_4H_4S和另外两种硫化合物,苯并噻吩和一种未确定的化合物(UN 1)。研究了在不同温度和气体时空速(GHSVs)下使用ZnO吸附剂去除硫化合物的方法。初级硫组分H_2S降至小于1 ppmv; COS没有显着降低; C_4H_4S的浓度完全不受影响。测定干燥气体中的平均NO和氨气浓度分别为8.2和2662 ppmv。两者均通过Ni催化剂成功转化为永久性气体。

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  • 来源
    《Energy & fuels》 |2010年第janaafeba期|1222-1233|共12页
  • 作者单位

    Hawaii Natural Energy Institute, University of Hawaii at Manoa, 1680 East-West Road, POST 109, Honolulu, Hawaii 96822;

    Hawaii Natural Energy Institute, University of Hawaii at Manoa, 1680 East-West Road, POST 109, Honolulu, Hawaii 96822;

    Hawaii Natural Energy Institute, University of Hawaii at Manoa, 1680 East-West Road, POST 109, Honolulu, Hawaii 96822;

    Hawaii Natural Energy Institute, University of Hawaii at Manoa, 1680 East-West Road, POST 109, Honolulu, Hawaii 96822;

    Hawaii Natural Energy Institute, University of Hawaii at Manoa, 1680 East-West Road, POST 109, Honolulu, Hawaii 96822;

    Hawaii Natural Energy Institute, University of Hawaii at Manoa, 1680 East-West Road, POST 109, Honolulu, Hawaii 96822;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
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