Journal of the Society of Inorganic Materials, Japan
Online ISSN : 2185-4378
ISSN-L : 1345-3769
12 巻 , 315 号
選択された号の論文の10件中1~10を表示しています
  • 高橋 実, 藤 正督, Yong-Sheng HAN
    2005 年 12 巻 315 号 p. 87-96
    発行日: 2005/03/01
    公開日: 2011/03/07
    ジャーナル フリー
  • 竹内 章浩, 田中 頼彦, 加藤 修一, 渡辺 隆行
    2005 年 12 巻 315 号 p. 97-105
    発行日: 2005/03/01
    公開日: 2011/03/07
    ジャーナル フリー
    Halons (bromofluorocarbons) are identified as ozone depleting substances and are forbidden to be produced since the end of 1993. Appropriate treatment method to decompose halon waste is required. A dry process to decompose halon with solid alkaline has been developed. Solid alkalis are prepared from reagents of CaO and MgO. Recovery of F became larger with an increase of MgO fraction in the solid alkaline. The recovery of Br became smaller with MgO fraction in the solid alkaline, since reactivity of Br with MgO was low. The diffusion of the gases produced by decomposition of halon through the product layer as well as the reactivity of the gases with the solid alkaline reactant are important for the halon decomposition treatment of the gases with the solid alkaline reactant.
  • 村松 重緒, 日吉 公男
    2005 年 12 巻 315 号 p. 106-114
    発行日: 2005/03/01
    公開日: 2011/03/07
    ジャーナル フリー
    Various burning conditions of paper sludge (PS) were examined for the purpose of waste-material recycling. Relationship between burning conditions and reaction products was investigated, and based on the results, optimal condition for recycling PS to use as a filler and a pigment of recycled paper was determined.
    The PS ash with high whiteness could be obtained through the general burning process at a high temperature more than 700°C for a long time more than 5 hours. However, this PS ash was not suitable for a paper-filler and a paper-pigment since the pH and electric conductivity values increased too much at the slurry-mixing step due to the formation of gehlenite with high hardness.
    Chemical changes of principal components of PS under a heating condition were examined by thermal analysis. Gehlenite was possibly formed from kaolin and calcium carbonate in PS via their thermally-caused change to mata-kaolin and calcium oxide. Since decarboxylation reaction depended on the partial pressure of carbon dioxide (CO2), transformation of calcium carbonate to calcium oxide could be suppressed by burning PS under CO2 atmosphere, although transforming reaction of kaolin to meta-kaolin hardly could because of independently from burning atmosphere. That is, decarboxylation temperature of calcium carbonate increased up to 800°C at CO2 concentration in air of 10% and 900°C at 100%.
    Consequently, proper burning condition of PS for recycling as a paper-filler and a paper-pigment was established as follows. Burning temperature is 700 to 750°C. Burning atmosphere is 10% of CO2 and 90% of air (20% of oxygen (O2) and 80% of nitrogen (N2))
  • 三国 彰, 魏 存弟, 小松 隆一, 池田 攻
    2005 年 12 巻 315 号 p. 115-121
    発行日: 2005/03/01
    公開日: 2011/03/07
    ジャーナル フリー
    ジオポリマー材料の知見を得るため中国カオリンとジョージアカオリンについてカオリンの熱変化とか焼物のアルカリ溶液への溶出特性について検討した.両カオリンはメタカオリンに変化し, か焼温度の上昇とともにAl-Siスピネル中間相をへてムライトとシリカに変化する.溶出試験は25, 80℃における0.1N水酸化ナトリウム溶液中でか焼したカオリンを溶出させることにより行なった.とくに溶出温度80℃においてSi+4.イオンおよびAl+3イオンは900℃および1100℃において特異的ピークが認められた.これらは比表面積値の傾向とは一致せず相変化とカオリンの分解に基づくものと考えられる.一方溶出温度25℃においては特異的なピークは認められなかった.550~800℃で調整されたメタカオリンにおいては溶出温度25, 80℃においてともに高い溶出量を示し, 比表面積の傾向と一致した.さらに中国カオリンにおいては非脱水物も高い溶出を示すことが確認された.
  • Dalibor KUCHAR, 粟田 浩季, 藤田 隆文, 小島 義弘, 平林 大介, 小澤 祥二, 松田 仁樹
    2005 年 12 巻 315 号 p. 122-130
    発行日: 2005/03/01
    公開日: 2011/03/07
    ジャーナル フリー
    For the purpose of recovering calcium resource from such solid wastes as coal burnt ash, iron slag, paper sludge, concrete sludge and shell waste, which involve calcium-derived compounds to a large extent, an attempt was made to extract calcium component with 6 organic acids : formic acid, acetic acid, propionic acid, oxalic acid, malonic acid and succinic acid.
    It was found that propionic acid was most effective among the employed 6 organic acids, in terms of extracted amount of calcium component. The CaO content in the extract was concentrated in the range of 70-94 mass% The enrichment of CaO extracted was correlated with pKa of organic acid. The increase in pKa value resulted in higher yield of CaO content with lower amount of the impurities such as SiO2, Al2O3 and Fe2O3.
    The HCl sorption capacity of CaO obtained by calcination of calcium propionate which was extracted from calcium-derived solid wastes employed in the present study, was 0.6-3.7 times higher than that of Ca (OH) 2. The increase in HCl sorption capacity of CaO obtained by the calcination of organic calcium compound may be attributed to a highly porous structure of the CaO.
  • 田中 実, 鈴木 蕃
    2005 年 12 巻 315 号 p. 131-137
    発行日: 2005/03/01
    公開日: 2011/03/07
    ジャーナル フリー
    Increasing accumulation of coal ash have been becoming a serious social problem in view of environmental loading, and its reuse or recycling of coal ash as raw materials of ceramics products is urgently required. Since the glass-ceramics of the CaO-Al2O3-SiO2 system have been promising as construction materials, we have investigated the preparation technique of the glass-ceramics of this system using coal ash by the bulk crystallization method. The glass-ceramics were investigated by means of scanning electron microscope (SEM), powder X-ray diffraction (XRD), and so on.
    Batches were prepared by mixing the starting materials in the various mass ratios of MIR : SiO2 : CaCO3 : FeS : Na2SO4 : C =150 : 0-18 : 30-60 : 0-4.5 : 0-6 : 0-1.5. Glass samples were produced by melting the batches at 1450°C. By those batch compositions, the glasses were homogeneously produced. They were reheated at 850°C for 1 hr to induce nucleation in the glasses. Further, the glasses were reheated at 1100°C for 2 hr, to make them to transform into glass-ceramics. The results of SEM photographs and powder XRD patterns of the obtained glass-ceramics showed that the homogeneous precipitations of the prismatic crystals (about 1×5μm) of anorthite (CaO·Al2O3·2SiO2) have occurred in the glasses by the bulk crystallization, accompanied by the precipitations of gehelenite (2CaO·Al2O3·SiO2) and/or nepheline (NaO2·Al2O3·25iO2).
  • 山村 博, 鈴木 智美, 柿沼 克良
    2005 年 12 巻 315 号 p. 138-142
    発行日: 2005/03/01
    公開日: 2011/03/07
    ジャーナル フリー
    It was tried to decompose benzene gas electrochemically by using electrochemical cell in the temperature range between 250 and 400°C, where 8 mol% Y2O3 doped ZrO2 (YSZ) well known as oxide-ion conductor was used for the electrolyte of electrochemical cell. Benzene gas was decomposed quantitatively to CO2 and H2O without any byproduct. The amounts of decomposed benzene increased with increasing the cell temperature or applied voltage (0-10 V) respectively, independent on the benzene concentration. The current increased with proportion to the square value of applied voltage.
  • 本橋 健司
    2005 年 12 巻 315 号 p. 143-147
    発行日: 2005/03/01
    公開日: 2011/03/07
    ジャーナル フリー
  • 宝田 恭之, 齋藤 美季, 森下 佳代子
    2005 年 12 巻 315 号 p. 148-154
    発行日: 2005/03/01
    公開日: 2011/03/07
    ジャーナル フリー
  • 三宅 通博
    2005 年 12 巻 315 号 p. 155-160
    発行日: 2005/03/01
    公開日: 2011/03/07
    ジャーナル フリー
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