石炭中の窒素と硫黄の化学形態と乾留過程での分配

  • 坪内 直人
    北海道大学大学院工学研究院附属エネルギー・マテリアル融合領域研究センター
  • 望月 友貴
    北海道大学大学院工学研究院附属エネルギー・マテリアル融合領域研究センター
  • 小野 洋平
    三菱化学(株)坂出事業所
  • 上坊 和弥
    住友金属工業(株)総合技術研究所

書誌事項

タイトル別名
  • Functional Forms of Nitrogen and Sulfur in Coals and Fate of Heteroatoms during Coal Carbonization
  • セキタン チュウ ノ チッソ ト イオウ ノ カガク ケイタイ ト カンリュウ カテイ デ ノ ブンパイ

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抄録

The functionalities of the nitrogen (coal-N) and sulfur (coal-S) present in three caking coals with carbon contents of 76-81 wt%-dry and the fate of these heteroatoms during coal carbonization have mainly been studied by the X-ray photoelectron spectroscopy (XPS) and with a fixed bed quartz reactor, respectively. The XPS measurements exhibit that about 80-90 % of the coal-N exists as pyrrolic-N and pyridinic-N, and the rest can be assigned to quaternary-N (pyridinic-N associated with the hydroxyl groups from phenols or carboxylic acids), whereas the coal-S consists of thiophenic-S, alkyl-S and FeS2, and the proportion of the former is as high as 60-70 %. When the coal sample is carbonized in He at a heating rate of 3°C/min, yield of N-containing species observed at 1000°C increases in the order of HCN ≤ tar-N < NH3 < N2 < oil-N < coke-N, regardless of the type of coal, and the latter two are present predominantly as NH4+ and in polynuclear aromatic structures, respectively. On the other hand, yield of S-containing species at 1000°C increases in the order of COS < CS2 < tar-S < oil-S < H2S < coke-S with all coals, and more than 95 % of the coke-S can be regarded as thiophenic-S. These tendencies are also observed with physical mixtures of each coal investigated. Possible mechanisms for the formation of gaseous N- or S-containing compounds in the carbonization process are discussed on the basis of the results of some thermodynamic calculations.

収録刊行物

  • 鉄と鋼

    鉄と鋼 98 (5), 161-169, 2012

    一般社団法人 日本鉄鋼協会

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