| ²é¿´: 590 | »Ø¸´: 3 | |||
| µ±Ç°Ö÷ÌâÒѾ´æµµ¡£ | |||
03240331Òø³æ (СÓÐÃûÆø)
|
[½»Á÷]
Çó¸ßÊÖ°ïæ·ÒëÂÛÎÄÕªÒª£¨60½ð±Ò£©
|
||
|
Çó¸ßÊÖ°ïæ·ÒëÂÛÎÄÕªÒª£¨60½ð±Ò£© Ñõ´úÒì·ð¶ûͪ£¨KIP£©ÊǺϳÉάÉúËØEµÄÖØÒªÖмäÌ壬Ëü¿ÉÒÔͨ¹ýÒì·ð¶ûͪÑõ»¯Éú³É¡£Ä¿Ç°ÓÐÁ½ÖֺϳÉ;¾¶£¬µÚÒ»Ìõ·ÏßΪ¦Á-Òì·ð¶ûͪÒì¹¹»¯Îª¦Â-Òì·ð¶ûͪ£¬È»ºóÔÙÑõ»¯¦Â-Òì·ð¶ûÍªÖÆµÃKIP£»µÚ¶þÌõ·ÏßΪֱ½ÓÑõ»¯¦Á-Òì·ð¶ûÍªÖÆ±¸¡£ÔÚµÚÒ»Ìõ·ÏßÖÐÓÉÓÚ¦Á-Òì·ð¶ûͪµÄ¹²éîЧӦ£¬Ê¹µÃ¦Á-Òì·ð¶ûͪÒì¹¹»¯Îª¦Â-Òì·ð¶ûͪµÄ¹ý³ÌÖÐÐèÒªºÜ¸ßµÄζȣ¬ÇÒ½öÓÐ4%×óÓÒµÄת»¯ÂÊ¡£ÁíÍ⴫ͳÉ϶ÔÒì·ð¶ûͪµÄ´ß»¯Ñõ»¯»ù±¾¶¼Êǰüº¬½ðÊôµÄ´ß»¯ÌåϵºÍÓлúÈܼÁ²ÎÓëµÄ·´Ó¦Ìåϵ£¬Õâ¶Ô»·¾³ÎÛȾ²úÉúÑÏÖØµÄÓ°Ïì¡£Òò´Ë±¾ÂÛÎĵÄÑо¿Ñ¡ÓÃÒÔ¦Á-Òì·ð¶ûֱͪ½ÓÑõ»¯µÄ·Ïߣ¬ÇÒ¸ù¾ÝÂÌÉ«»¯Ñ§µÄÔÔò£¬ÒÔÑõÆøÎªÑõ»¯¼Á£¬ÓÃÒ»ÖÖÎÞ½ðÊô²ÎÓëµÄN¨CôÇ»ùÁÚ±½¶þ¼×õ£Ñǰ·Îª´ß»¯¼Á´ß»¯¦Á-Òì·ð¶ûͪ£¬ÎªÑõ´úÒì·ð¶ûͪµÄÖÆ±¸ÌṩһÌõȫеÄ;¾¶¡£ ±¾ÂÛÎÄÊ×ÏȲÉÓÃN¨CôÇ»ùÁÚ±½¶þ¼×õ£Ñǰ·Îª´ß»¯¼Á£¬ÔÚÓлúÈܼÁºÍÓлúÖú´ß»¯¼ÁµÄ²ÎÓë϶ԦÁ-Òì·ð¶ûͪ½øÐзǽðÊôµÄ´ß»¯Ñõ»¯Ñо¿£¬ÔÚÕû¸ö·´Ó¦ÖÐÍêÈ«±ÜÃâÁ˽ðÊôµÄ²ÎÓ룬ÇÒ·´Ó¦µÍ£¬ÄܺÄÉÙ£¬²Ù×÷·½±ã£¬Òò¶øÊÇÒ»ÖÖÂÌÉ«µÄÑõ»¯Â·Ïߣ¬½øÒ»²½¶ÔÓ°Ïì·´Ó¦µÄÒòËØÈçζȡ¢´ß»¯Á¿µÈ½øÐÐÓÅ»¯£¬²úÎïµÄÑ¡ÔñÐÔ¿ÉÒÔ´ïµ½90%×óÓÒ¡£ Æä´Î£¬±¾ÂÛÎÄ»¹¿¼²ìÁËÔÚÎÞÈܼÁºÍ²»¼ÓÈκεÄÖú´ß»¯¼ÁµÄÌõ¼þ϶ԦÁ-Òì·ð¶ûͪµÄ´ß»¯Ñõ»¯£¬·¢ÏÖ½öÓô߻¯Á¿µÄN¨CôÇ»ùÁÚ±½¶þ¼×õ£Ñǰ·¼´¿ÉÓÐЧµÄ´ß»¯Ñõ»¯¦Á-Òì·ð¶ûͪ£¬ÔÚ60¶ÈµÄζÈÏ£¬²úÎïµÄÑ¡ÔñÐԿɳ¬¹ý75%¡£ ×îºó£¬±¾ÂÛÎĶÔÕâÒ»·´Ó¦¹ý³ÌµÄ»úÀí½øÐÐÁËÑо¿£¬Í¨¹ý¶Ô·´Ó¦¹ý³ÌµÄ·ÖÎö£¬½áºÏESI-MSºÍGC-MSµÈ¶Ô·´Ó¦²úÎï¼°·´Ó¦ÖмäÌåµÄ¼ì²â¡¢ÒÔ¼°Ïà¹Øµ×ÎïµÄʵÑé¶Ô±ÈÊֶΣ¬Ìá³öÁ˦Á-Òì·ð¶ûͪ·Ç½ðÊô´ß»¯Ñõ»¯µÄ×ÔÓÉ»ù·´Ó¦»úÀí£¬²¢¡£Õâ¸ö»úÀíµÄÌá³ö£¬²»½ö½âÊÍÁË·´Ó¦Öи±²úÎï²úÉúµÄÔÒò£¬Îª½øÒ»²½Ìá¸ßÄ¿±ê²úÎïµÄʵÑéÉè¼ÆÌṩÁËеķÏߣ¬Í¬Ê±Ò²ÎªÍƲâºÍÑéÖ¤Ïà¹ØÌåϵµÄÑõ»¯·´Ó¦»úÀíÌṩÁËеÄ˼·¡£ |
» ²ÂÄãϲ»¶
081700»¯Ñ§¹¤³ÌÓë¼¼Êõ Ò»Ö¾Ô¸Öк£Ñó 323 Çóµ÷¼ÁѧУ
ÒѾÓÐ12È˻ظ´
385·Ö ÉúÎïѧ£¨071000£©Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
²ÄÁÏר˶283Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
0703Çóµ÷¼Á383·Ö
ÒѾÓÐ5È˻ظ´
323Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
26¿¼Ñе÷¼Á0710 0860
ÒѾÓÐ8È˻ظ´
081700ѧ˶£¬323·Ö£¬Ò»Ö¾Ô¸Öйúº£Ñó´óѧÇóµ÷¼ÁѧУ
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤´óѧ£¬³õÊԳɼ¨350Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸0817»¯Ñ§¹¤³ÌÓë¼¼Êõ£¬Çóµ÷¼Á
ÒѾÓÐ22È˻ظ´
085600£¬×¨Òµ¿Î»¯¹¤ÔÀí£¬321·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
sallyyjy
½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 1075.8
- É¢½ð: 102
- Ìû×Ó: 467
- ÔÚÏß: 9.2Сʱ
- ³æºÅ: 566850
- ×¢²á: 2008-05-31
2Â¥2010-01-19 15:36:59
2008000465
ľ³æ (СÓÐÃûÆø)
- Ó¦Öú: 1 (Ó×¶ùÔ°)
- ½ð±Ò: 2236.8
- Ìû×Ó: 281
- ÔÚÏß: 124.4Сʱ
- ³æºÅ: 885733
- ×¢²á: 2009-10-27
- ÐÔ±ð: MM
- רҵ: ¸ß·Ö×Ӻϳɻ¯Ñ§
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
03240331(½ð±Ò+20):·Ç³£¸Ðл£¬Âé·³Äú°ïÎÒ°ÑʣϵķÒëһϰ¡¡£Ð»Ð»ÄúÁË 1-23 13:18
03240331(½ð±Ò+20):·Ç³£¸Ðл£¬Âé·³Äú°ïÎÒ°ÑʣϵķÒëһϰ¡¡£Ð»Ð»ÄúÁË 1-23 13:18
|
Oxo-isophorone (KIP)prepared by isophorone oxidation is an important intermediate of synthesis of vitamin E. There are two kinds of synthetic pathway for KIP, the first route is to isomerize ¦Á-isophorone into a ¦Â-isophorone, and then oxidize ¦Â-isophorone into the product; the second route is direct oxidation of ¦Á-iso-Isophorone into the product. In the first route, the isomerization process of ¦Á-isophorone into a ¦Â-isophorone requires high temperatures, and only about 4% of the conversion was obtained for the conjugate effect of ¦Á-isophorone. Moreover, the traditional catalytic oxidation system of isophorone contains metal and organic solvents, which cause environmental pollution. Therefore, this paper selected the direct oxidation route to synthesize ¦Á-isophorone, and according to the principles of green chemistry, oxygen was used as the oxidant, with non-metal N-hydroxy-phthalimide as catalyst, for preparation of Isophorone. ÏȵÚÒ»¶Î£¬Ì«³¤ÁË |
3Â¥2010-01-22 08:14:55
2008000465
ľ³æ (СÓÐÃûÆø)
- Ó¦Öú: 1 (Ó×¶ùÔ°)
- ½ð±Ò: 2236.8
- Ìû×Ó: 281
- ÔÚÏß: 124.4Сʱ
- ³æºÅ: 885733
- ×¢²á: 2009-10-27
- ÐÔ±ð: MM
- רҵ: ¸ß·Ö×Ӻϳɻ¯Ñ§
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
03240331(½ð±Ò+20):ÐÁ¿àÁË 1-24 18:50
03240331(½ð±Ò+20):ÐÁ¿àÁË 1-24 18:50
| In this paper, firstly we studied the non-metallic catalytic oxidation of ¦Á-isophorone using N-hydroxy-phthalimide as a catalyst in the presence of organic co-catalysts and solvents. The completely avoiding of metal usage, a low energy consumption and convenient operation make the oxidation route a green process. Moreover, by optimizing reaction factors such as temperature, catalyst amount, etc., high product selectivity to 90% can be reached.Secondly, the paper examined the catalytic oxidation of ¦Á-isophorone in the absence of solvent and co-catalyst. We found only catalytic amount of N-hydroxy phthalimide can be an effective for catalytic oxidation of ¦Á-isophorone at 60¡æ, and the product selectivity can exceed 75%.Finally, this paper studies the mechanism of this reaction by analysis of reaction process, using ESI-MS and GC-MS technique to monitor reaction products and the reaction intermediates, and comparison of related substrates. We proposed the non-metallic ¦Á-isophorone catalytic oxidation is a free radical reaction. The mechanism proposed not only explains the cause of byproduct formed in the reaction which can provide new synthetic route of improving target product, but also provides a new route to speculate and verify mechanism of other oxidation reactions related. |
4Â¥2010-01-23 19:22:25














»Ø¸´´ËÂ¥