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Fe2O3MoO3Sb2O3ÌåϵÖУ¬ÔÚ½øÐÐÈÈ´¦Àí֮ǰ¶Ô»ìºÏÎïµÄÑÐÄ¥ÓÐÖúÓÚÑõ»¯ÌàµÄ·ÖÉ¢¡£300 ¡æ±íÃæÒÑÃ÷ÏԹ۲쵽Sb2O3¶ÔFe2O3ºÍMoO3µÄ¹Ì̬ÈóʪÏÖÏó¡£400 ¡æÊ±ÈýÑõ»¯¶þÌ࿪ʼÑõ»¯ÎªËÄÑõ»¯¶þÌ࣬ͬʱSb2O3¶ÔFe2O3ºÍMoO3µÄ¹Ì̬Èóʪ¼±¾çÔöÇ¿£¬Ö±µ½500 ¡æÊ±£¬Sb2O3±»ÍêÈ«Ñõ»¯¡£ÓÉÓÚSb2O3¾ßÓм«Ç¿µÄÈóʪЧ¹û£¬MoO3µÄ±íÃæÓÉÓÚ±»Sb2O3°ü¸²£¬ÄÑÒÔÔÙ¶ÔFe2O3±íÃæ½øÐйÌ̬Èóʪ£¬Í¬Ê±Ò²·Á°­ÁËFe2O3ºÍMoO3µÄ¹ÌÏà·´Ó¦Éú³ÉFe2(MoO4)3£¬½«Æä¿ªÊ¼Éú³ÉµÄζȼ¸ºõÌá¸ßÁË300 ¡æ£¨¼´700 ¡æ£©¡£°éËæ×ÅFe2(MoO4)3µÄÐγɣ¬FeSbO4ÎïÏà³öÏÖ£¬Õâ±ÈSb2O3¶ÔFe2O3Ë«×é·ÖÌåϵÖÐFeSbO4µÄÉú³ÉζȽµµÍÁËÔ¼100 ¡æ£¬ÕâÊÇÓÉÓÚFe2(MoO4)3¶ÔFeSbO4µÄÉú³ÉÆðµ½ÁË´ß»¯×÷Ó᣼״¼Ñ¡ÔñÑõ»¯·´Ó¦±íÃ÷£ºSb2O3ºÍSb2O4µÄ¹Ì̬ÈóʪÏÖÏó¶ÔFeMoO´ß»¯¼Á¾ßÓÐÏÔÖøµÄ¡°Öж¾¡±Ð§Ó¦¡£

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Milling mixture is benefit for the dispersion of Sb2O3 before heat treatment in the reaction system of Sb2O3MoO3Fe2O3. it is obviously observed that Sb2O3 solid wets Fe2O3 and MoO3 at 300¡æ. Sb2O3 is oxidized into sb204 at 400¡æ, and the solid wetting of Sb2O3 to Fe2O3 and MoO3 increases simultaneously until Sb2O3 is fully oxidized at 500¡æ. MoO3 is coated by Sb2O3 due to strong wetting effect of Sb2O3, and it can not wet Fe2O3. the solid reaction into Fe2(MoO4)3 between Fe2O3 and MoO3 is also impeded, and the initial reaction temperature rises by 300¡æ (i.e. 700¡æ). FeSbO4 phase occurs with the formation of Fe2(MoO4)3.It indicates that the formation temperature of  FeSbO4 while Fe2(MoO4)3 exists is lower by 100¡æ than that in the dual ¨Ccomponent reaction system of Sb2O3 and Fe2O3 due to the catalysis effect of Fe2(MoO4)3 to FeSbO4. carbinol selective oxidization reaction shows that the solid wetting of Sb2O3 and Sb2O4 has a significant poisonous effect on the catalyst of FeO.
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in theFe2O3  MoO3   Sb2O3 system, before carrying on the heat treatment to the mixture attrition is helpful to the antimony oxide dispersion. 300 ¡æ surfaces observed Sb2O3 obviously to Fe2O3 and the MoO3 solid state moist phenomenon.
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400 ¡æÊ±ÈýÑõ»¯¶þÌ࿪ʼÑõ»¯ÎªËÄÑõ»¯¶þÌ࣬ͬʱSb2O3¶ÔFe2O3ºÍMoO3µÄ¹Ì̬Èóʪ¼±¾çÔöÇ¿£¬Ö±µ½500 ¡æÊ±£¬Sb2O3±»ÍêÈ«Ñõ»¯¡£ÓÉÓÚSb2O3¾ßÓм«Ç¿µÄÈóʪЧ¹û£¬MoO3µÄ±íÃæÓÉÓÚ±»Sb2O3°ü¸²£¬ÄÑÒÔÔÙ¶ÔFe2O3±íÃæ½øÐйÌ̬Èóʪ£¬Í¬Ê±Ò²·Á°­ÁËFe2O3ºÍMoO3µÄ¹ÌÏà·´Ó¦Éú³ÉFe2(MoO4)3£¬½«Æä¿ªÊ¼Éú³ÉµÄζȼ¸ºõÌá¸ßÁË300 ¡æ£¨¼´700 ¡æ£©¡£°éËæ×ÅFe2(MoO4)3µÄÐγɣ¬FeSbO4ÎïÏà³öÏÖ£¬Õâ±ÈSb2O3¶ÔFe2O3Ë«×é·ÖÌåϵÖÐFeSbO4µÄÉú³ÉζȽµµÍÁËÔ¼100 ¡æ£¬ÕâÊÇÓÉÓÚFe2(MoO4)3¶ÔFeSbO4µÄÉú³ÉÆðµ½ÁË´ß»¯×÷Ó᣼״¼Ñ¡ÔñÑõ»¯·´Ó¦±íÃ÷£ºSb2O3ºÍSb2O4µÄ¹Ì̬ÈóʪÏÖÏó¶ÔFeMoO´ß»¯¼Á¾ßÓÐÏÔÖøµÄ¡°Öж¾¡±Ð§Ó¦¡£
At 400 ¡æ , trioxide two stibium start to oxidize for the tetroxide two stibium, simultaneously Sb2O3 moist strengthens suddenly to Fe2O3 and the MoO3 solid state, until 500 ¡æ, Sb2O3 is oxidized completely. Because Sb2O3 has the greatly strengthened moist effect, the MoO3 surface as a result of by the Sb2O3 gable, is carried on to the Fe2O3 surface the solid state to be moist again with difficulty, simultaneously has also hindered Fe2O3 and the MoO3 solid phase responds produces Fe2(MoO4)3, started the temperature which it produced to enhance nearly 300 ¡æ (i.e. 700 ¡æ). Follows the Fe2(MoO4)3 formation, the FeSbO4 phase is appearing, this was the FeSbO4 production temperature reduced compared to Sb2O3 to the Fe2O3 two-group fission approximately 100 ¡æ, this was as a result of Fe2(MoO4)3 to the FeSbO4 production catalytic effect. The methyl alcohol selective oxidation response indicated: Sb2O3 and the Sb2O4 solid state moist phenomenon catalyst has ¡°the poison¡± obviously to Fe  Mo  the O the effect.
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3Â¥2008-06-05 21:44:42
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