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Abstract
The stoichiometry, temperature dependence, and the effect of atmosphere for the thermal decomposition of Pt and Pd ammine complexes exchanged into zeolite Y were investigated by thermogravimetry. It was found that (a) the maximum rate of reduction of Pt and Pd ammine Y occurred at 300 and 250 ¡ãC, respectively; (b) decomposition of Pt ammine Y in air leads to formation of Pt metal¡ªair is essentially an inert medium, although the oxidation of evolved NH3 is catalyzed by Pt; Pd is only partially reduced to metal when Pd ammine Y is decomposed in air; (c) decomposition in H2 effects reduction at much lower temperatures; (d) acid sites in the zeolite are always generated stoichiometrically by the decomposition of Pt and Pd ammines, whether in hydrogen, helium, or air. The maximum rate of reduction of Pt ammine Y at 300 ¡ãC correlates with reported maxima in dehydrogenation activity and Pt dispersion. In this study, the 300 ¡ãC calcined catalysts showed maximum n-hexane dehydrocyclization activity and selectivity as well as cyclohexane dehydrogenation.
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guoyuping(½ð±Ò+4): 2011-05-04 14:59:32
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Originally posted by penfee at 2011-04-28 19:03:50:
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guoyuping(½ð±Ò+5): Ì«¸ÐлÄãÁË£¡ 2011-04-29 08:03:19
zhangwengui330(C-EPI+1): ллӦÖú£¡£¡ 2011-05-02 13:25:43
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Originally posted by guoyuping at 2011-04-28 19:57:33:
Âí¸¥Â¯±ºÉÕʱ£¬Â¯ÃÅÎÒÌØÒâû¹ØÌ«½ôÁôÁËÒ»µã·ì£¬ÊDz»Êǵ±ÀïÃæÑõÆøºÄµôÖ®ºóÍⲿ¿ÕÆø½øÈ¥ÁË£¬ÑùÆ·±ºÉÕ³ä·Ö£¬ËùÒÔ·Ö×ÓɸÍâ±íÃæ²ÐÁôµÄPt(NH3)42+Àë×Ó±ä³É²¬µÄÑõ»¯ÎïÐÎʽÁË£¬ËùÒÔ±äÑÕÉ«ÁË£¿
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ÒªÏë½âÊÍÕâÀïµÄÔ­Òò£¬ºÜÓбØÒªÈ¥Á˽âÒ»ÏÂ[Pt(NH3)4]2+Àë×ÓÔÚ±ºÉÕ¹ý³ÌÖÐÊÇÈçºÎ·Ö½âµÄ¡£ÔÚÍøÉÏÕÒÁËһƪÎÄÏ×£¬ºÜÏ꾡µØÃèÊöÁËÀë×Ó½»»»µÄ[Pt(NH3)4]2+Àë×ÓµÄÈÈ·Ö½â¹ý³Ì£¬¶ÔÎÒÃǺÜÓÐÆô·¢£¬¿ÉÒÔÓÃÀ´½âÊÍÂ¥Ö÷Åöµ½µÄÏÖÏó¡£ÎÄÏ×¼û¸½¼þ1.
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When the thermal decomposition was monitoredby mass spectrometry it became clear that half of theamine ligands of the [Pt(NH3)4]2+complex were released at the first step, while the remaining ones were released in another step. When NO was formed in the second step, it was temporarily adsorbed in the zeolite framework [8]

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