±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 836  |  »Ø¸´: 19
¡¾½±Àø¡¿ ±¾Ìû±»ÆÀ¼Û17´Î£¬×÷Õßa410731466Ôö¼Ó½ð±Ò 16 ¸ö
µ±Ç°Ö÷ÌâÒѾ­´æµµ¡£

a410731466

½û³æ (ÕýʽдÊÖ)


[×ÊÔ´] CATALYST SEPARATION, RECOVERY AND RECYCLING

CATALYST SEPARATION, RECOVERY AND RECYCLING
ROBERT P. TOOZE
Fife, Scotland
Edited by
Fife, Scotland
             and
EaStCHEM, School of Chemistry, University of St. Andrews,S  t. Andrews,
DAVID J. COLE-HAMILTON
CATALYST SEPAR P P A R R TION, RECOVE A A RY R R
Sasol Technology (UK) Ltd., St. Andrews,
Chemistry and Process Design


CHAPTER 1  HOMOGENEOUS CATALYSIS ¨C ADVANTAGES AND
PROBLEMS
1.1  Catalysis
1.2  Catalyst Stability
1.2.1   THERMALLY INDUCED DECOMPOSITION
1.2.2   CHEMICALLY INDUCED DECOMPOSITION
1.2.3   PHYSICAL LOSS FROM THE PROCESS
1.3 Layout of the Book
1.4 References
CHAPTER 2  CLASSICAL HOMOGENEOUS CATALYST SEPARATION
TECHNOLOGY
2.1.1 Coverage of Chapter
2.2   General Process Considerations
2.3   Everything is a Reactor
2.4   Overview of Separation Technologies
2.4.1 TRADITIONAL COBALT WITH CATALYST DECOMPOSITION
2.4.2  UNION CARBIDE-DAVY GAS RECYCLE PROCESS.
2.4.3 LIQUID RECYCLE
2.4.4 BIPHASIC SYSTEMS; WATER-ORGANIC
2.4.5 INDUCED PHASE SEPARATION
2.4.6 NON-AQUEOUS PHASE SEPARATION
2.4.6.1 NAPS Using a Non-Polar Catalyst
2.4.6.2  NAPS Using a Polar Catalyst
2.4.6.3 Ligand Structure and Solubility Properties
2.5  Hypothetical processes - How Might the Product be Separated from the Catalyst
2.5.1 PROPENE HYDROFORMYLATION
2.5.2 1-OCTENE HYDROFORMYLATION
2.5.3 ALLYL ALCOHOL
2.5.4 METHOXYVINYLNAPHTHALENE
2.5.5  SEPARATION TECHNOLOGY FOR LESS STABLE CATALYSTS  
2.5.5.1 Mitsubishi TPPO/TPP Separation
2.5.5.2 Organic Polymer for Catalyst Stabilization
2.6 Real-World Complications
2.6.1  ORGANOPHOSPHORUS LIGAND DEGRADATIONS
2.6.1.1 Oxidation 2.6.1.2 Alkyldiarylphosphine Formation
2.6.1.3 Ligand Scrambling
2.6.1.4 Phosphine Reactions with Conjugated Systems
2.6.1.5 Phosphite Oxidation
2.6.1.6 Simple Phosphite Hydrolysis
2.6.1.7 Poisoning Phosphite Formation
2.6.1.8 Aldehyde Acid Formation
2.6.1.9 Acidity Control
2.6.2  SEPARATING BYPRODUCTS FROM REACTANTS OR PRODUCTS
2.6.2.1 Alkene Hydrogenation
2.6.2.2Alkene Isomerization
2.6.2.3 Aldehyde Dimerization and Trimerization
2.6.2.4 Formation of Conjugated Carbonyls
2.6.3 INTRINSIC CATALYST DEACTIVATION
2.7 Further Separation Challenges
2.7.1  RECOVERY OF METAL VALUES FROM A SPENT CATALYST
2.7.1.1 Catalyst Containment and Capture Technologies
2.8 Concluding Remarks
2.9 References
CHAPTER 3  SUPPORTED CATALYSTS
Immobilisation of Tailor-made Homogeneous Catalysts
3.1 Introduction
3.2  Short Historical Overview
3.3   Polystyrene Supported Catalysts
3.4   Silica Supported Catalyst
3.5   Catalysis in Interphases
3.6   Ordered Mesoporous Support
3.7   Non-covalently Supported Catalysts
3.8   Supported Aqueous Phase Catalysis
3.9 Process Design [71]
3.10 Concluding Remarks  
3.11 References
CHAPTER 4       SEPARATION BY SIZE-EXCLUSION FILTRATION
Homogeneous Catalysts Applied in Membrane Reactors
4.1 Introduction
4.2 Reactors
4.2.1 DEAD-END FILTRATION REACTORS
4.2.2  CROSS-FLOW FILTRATION REACTORS
4.3 Membranes
4.3.1  CLASSIFICATION OF FILTRATION TYPES
4.4  Dendrimer Supported Catalysts
4.4.1 KHARASCH ADDITION REACTION
4.4.2 ALLYLIC SUBSTITUTION REACTIONS
4.4.3 HYDROVINYLATION REACTION
4.4.4 HYDROGENATION
4.4.5 MICHAEL ADDITION REACTION
4.5 Dendritic Effects
4.6  Unmodified or Non-dendritic Catalysts  
4.6.1 HYDROGENATION
4.6.2 PHASE TRANSFER CATALYSIS
4.7  Soluble Polymer Supported Catalysts
4.8  Concluding Remarks
4.9 References
CHAPTER 5  BIPHASIC SYSTEMS: WATER ¨C ORGANIC
4.3.2 MEMBRANE MATERIALS  
5.2.1 GENERAL
5.2.2 BIPHASIC SYSTEMS
5.2.3 AQUEOUS BIPHASIC CATALYSIS
5.2.3.2    Aqueous-phase Catalysis as a Unit Operation
5.2.4    EXAMPLES OF AQUEOUS BIPHASIC CATALYSIS
5.2.4.1   Hydroformylation (Ruhrchemie/Rhône-Poulenc[RCH/RP] process
5.2.4.2 Other Industrially Used Aqueous-biphasic Processes
5.2.4.3   Short Overview of Other Reaction
5.2.5   OTHER PROPOSALS FOR WATER - BIPHASIC SYSTEMS 5.2.6 INTERLUDE - BIPHASIC SYSTEMS: ORGANIC-ORGANIC
5.3  Recycle and Recovery of Aqueous Catalysts
5.3.1 RECYCLING
5.3.2 RECOVERY
5.3.3   ECONOMICS OF THE PROCESS
5.3.4   ENVIRONMENTAL ASPECTS
5.4 Concluding Remarks
5.5   References
5.1 Introduction
5.2.3.1  Water as a Solvent
5.2 Immobilization with the Help of Liquid Supports
CHAPTER 6  FLUOROUS BIPHASIC CATALYSIS
6.1 Introduction
6.2 Alkene Hydrogenation
6.3 Alkene Hydrosilation
6.4 Alkene Hydroboration
6.5   Alkene Hydroformylation
6.6 Alkene Epoxidation
6.7  Other Oxidation Reactions
6.8 Allylic Alkylation
6.9 Heck, Stille, Suzuki , Sonagashira and Related Coupling Reactions
6.10 Asymmetric Alkylation of Aldehydes  
6.11  Miscellaneous Catalytic Reactions
6.12 Fluorous Catalysis Without Fluorous Solvents
6.13 Continuous Processing
6.14 Process Synthesis for the Fluorous Biphasic Hydroformylation of
1-Octene
6.15  Conclusions
6.16 Acknowledgement  
6.17 References
CHAPTER 7  CATALYST RECYCLING USING IONIC LIQUIDS
7.1 Introduction
7.1.1  INTRODUCTION TO IONIC LIQUIDS
7.1.2 INTRODUCTION TO TRANSITION METAL CATALYSIS IN IONIC
LIQUIDS
7.1.3  MULTIPHASIC CATALYSIS WITH IONIC LIQUIDS ¨C ENGINEERING
ASPECTS
7.2  Liquid-liquid Biphasic, Rh-catalysed Hydroformylation Using Ionic
Liquids
7.3 Rhodium Catalysed Hydroformylation Using Supported Ionic Liquid
Phase SILP) Catalysis
7.3.1  SUPPORTED IONIC LIQUIDS BY CHEMICAL BONDS
7.3.2  SUPPORTED IONIC LIQUIDS BY IMPREGNATION
7.4  Costs And Economics
7.5  Conclusions
7.6 References CHAPTER 8  SUPERCRITICAL FLUIDS
Compressed Gases as Mobile Phase and Catalyst Support
8.1 Introduction to supercritical fluids
8.2 Applications of scCO2 in Catalyst Immobilisation
8.2.1  CO2 AS THE ONLY MASS SEPARATING AGENT
8.2.2  BIPHASIC SYSTEMS CONSISTING OF CO2 AND LIQUID PHASES ...223
8.2.2.1  Water as the Liquid Phase
8.2.2.2  Poly(ethyleneglycol) (PEG) as the Liquid Phase
8.2.2.3 Ionic Liquids as the Liquid Phase
8.2.3 BIPHASIC SYSTEMS CONSISTING OF CO2 AND SOLID PHASES 230
8.2.3.1 Inorganic Supports
8.2.3.2 Organic Polymer Supports
8.4  Summary
8.5 References
CHAPTER 9  AREAS FOR FURTHER RESEARCH
9.1 Introduction
9.2 Conventional Separation Methods (See Chapter 2
9.3  Catalysts on Insoluble Supports (Chapter 3)
9.4  Catalysts on Soluble Supports (Chapter 4
9.5 Aqueous Biphasic Catalysis (Chapter 5)
9.6  Fluorous Biphasic Catalysis (Chapter 6)
9.7 Reactions Involving Ionic Liquids (Chaoter 7
9.8 Reactions Using Supercritical Fluids (Chapter 8
9.9  Conclusions
9.10 References
8.3 Economic Evaluation and Summary
8.3.1 POTENTIAL FOR SCALE-UP
http://www.namipan.com/d/83eced65f9dad053e728a7621711a43fa2107035e5ab5800
»Ø¸´´ËÂ¥
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

dewey

ľ³æ (ÕýʽдÊÖ)


¡ï¡ï¡ï¡ï¡ï ÎåÐǼ¶,ÓÅÐãÍÆ¼ö

Thanks for your share
8Â¥2009-02-19 08:35:39
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

heflylife

ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)


¡ï¡ï¡ï ÈýÐǼ¶,Ö§³Ö¹ÄÀø

thanks
10Â¥2009-02-19 08:54:09
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

yyuchuan

½ð³æ (ÕýʽдÊÖ)


¡ï¡ï¡ï¡ï¡ï ÎåÐǼ¶,ÓÅÐãÍÆ¼ö

11Â¥2009-02-19 09:50:27
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

³ÂÈðÏã

Í­³æ (СÓÐÃûÆø)


¡ï¡ï¡ï¡ï¡ï ÎåÐǼ¶,ÓÅÐãÍÆ¼ö

thanks
13Â¥2009-02-19 16:49:17
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

zhouchangjiang

½ð³æ (СÓÐÃûÆø)


¡ï¡ï¡ï ÈýÐǼ¶,Ö§³Ö¹ÄÀø

thanks
17Â¥2009-02-22 12:57:44
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

mland

ľ³æ (ÖøÃûдÊÖ)


¡ï¡ï¡ï¡ï¡ï ÎåÐǼ¶,ÓÅÐãÍÆ¼ö

thanks
±àÕß»¹ÓÐһƪͬÌâÄ¿µÄScienceÎÄÕÂ
19Â¥2009-03-07 10:54:08
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
¼òµ¥»Ø¸´
zyhou2Â¥
2009-02-17 20:45   »Ø¸´  
 
huazhang23Â¥
2009-02-17 22:59   »Ø¸´  
 
liang494Â¥
2009-02-18 08:40   »Ø¸´  
 Ð»Ð»·ÖÏí!
QWD5Â¥
2009-02-18 19:41   »Ø¸´  
 
chensthjkl6Â¥
2009-02-18 19:52   »Ø¸´  
 
ryfallen7Â¥
2009-02-19 08:12   »Ø¸´  
 
sosolala9Â¥
2009-02-19 08:45   »Ø¸´  
 
lingliaopiao12Â¥
2009-02-19 10:30   »Ø¸´  
 
kwang78814Â¥
2009-02-21 17:16   »Ø¸´  
Ö§³ÖÏ£¡£¡£¡
kwang78815Â¥
2009-02-21 17:16   »Ø¸´  
Ö§³ÖÏ£¡£¡£¡
2009-02-21 18:45   »Ø¸´  
 
daniel58218Â¥
2009-03-02 15:18   »Ø¸´  
 
arielroy20Â¥
2009-03-08 08:28   »Ø¸´  
 
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ a410731466 µÄÖ÷Ìâ¸üÐÂ
¡î ÎÞÐǼ¶ ¡ï Ò»ÐǼ¶ ¡ï¡ï¡ï ÈýÐǼ¶ ¡ï¡ï¡ï¡ï¡ï ÎåÐǼ¶
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] 315·Ö 085602 Çóµ÷¼Á +14 26¿¼ÑÐÉϰ¶°æ26 2026-04-02 14/700 2026-04-03 11:29 by qqq850810
[¿¼ÑÐ] Çóµ÷¼Á +3 ÐÄÏëÊÂ³É¿É 2026-04-03 3/150 2026-04-03 11:22 by wangjy2002
[¿¼ÑÐ] Ò»Ö¾Ô¸Öйú¿ÆÑ§Ôº´óѧ265Çóµ÷¼Á +9 Ìñµ­ye 2026-03-31 10/500 2026-04-03 11:10 by txp1986
[¿¼ÑÐ] 279Çóµ÷¼Á +6 qazplm0852 2026-04-02 6/300 2026-04-03 10:03 by À¶ÔÆË¼Óê
[¿¼ÑÐ] 266·Ö£¬Ò»Ö¾Ô¸µçÆø¹¤³Ì£¬±¾¿Æ²ÄÁÏ£¬Çó²ÄÁÏרҵµ÷¼Á +8 ÍÛºôºßºôºß 2026-04-02 8/400 2026-04-03 10:00 by hypershenger
[¿¼ÑÐ] ¸´ÊÔµ÷¼Á +3 bvzz 2026-04-01 3/150 2026-04-03 09:47 by À¶ÔÆË¼Óê
[¿¼ÑÐ] ÖØÇì´óѧ²ÄÁÏÓ뻯¹¤085600£¬³õÊÔ370+£¬ÇóÇóµ÷¼Á½¨Òé +8 shzhou_ 2026-04-01 9/450 2026-04-03 09:31 by À¶ÔÆË¼Óê
[¿¼ÑÐ] ÉúÎïѧ308·ÖÇóµ÷¼Á£¨Ò»Ö¾Ô¸»ª¶«Ê¦´ó£© +6 ÏàÐűػá¹ââÍòÕ 2026-03-31 7/350 2026-04-02 23:16 by JourneyLucky
[¿¼ÑÐ] 272Çóµ÷¼Á£¬½ÓÊÜ¿çרҵµ÷¼Á£¡ +4 ÏÐÓ㬠2026-03-31 4/200 2026-04-02 11:18 by guyan1000
[¿¼ÑÐ] 385·Ö ÉúÎïѧ£¨071000£©Çóµ÷¼Á +6 qf626 2026-04-01 6/300 2026-04-02 10:39 by guoweigw
[¿¼ÑÐ] 0817»¯¹¤Ñ§Ë¶µ÷¼Á +11 ŬÁ¦Éϰ¶ÖУ¡ 2026-03-31 11/550 2026-04-01 20:30 by Àµ´ºÑÞ
[¿¼ÑÐ] Ò»Ö¾Ô¸±±½»²ÄÁϹ¤³Ì×Ü·Ö358 +5 cs0106 2026-04-01 7/350 2026-04-01 11:45 by wangjy2002
[¿¼ÑÐ] 080500-315·Ö¸´ÊÔµ÷¼Á +9 Éϰ¶3821 2026-03-31 9/450 2026-03-31 17:29 by ÌÆãå¶ù
[¿¼ÑÐ] ¿¼Ñе÷¼ÁÇóÖú +7 13287130938 2026-03-31 7/350 2026-03-31 16:39 by 690616278
[¿¼ÑÐ] Ò»Ö¾Ô¸Äϲý´óѧ324Çóµ÷¼Á +6 hanamiko 2026-03-29 6/300 2026-03-31 16:35 by hypershenger
[¿¼ÑÐ] Ò»Ö¾Ô¸´óÁ¬Àí¹¤´óѧ£¬»úе¹¤³Ìѧ˶£¬341 +3 Î÷¹ÏÌïµÄÊØÍûÕß 2026-03-30 3/150 2026-03-31 11:08 by asdfzly
[¿¼ÑÐ] 262Çóµ÷¼Á +7 ZZ..000 2026-03-30 8/400 2026-03-31 10:05 by cal0306
[¿¼ÑÐ] ¼ª´óÉúÎïѧ326·ÖÇóµ÷¼Á +3 sunnyupup 2026-03-31 3/150 2026-03-31 09:28 by longlotian
[Óлú½»Á÷] ¼×»ùÑǻǻÇËáÄÆºÍ¼×»ù»ÇËáõ¥·´Ó¦»úÀí 10+3 kaobao456 2026-03-29 4/200 2026-03-30 23:16 by nBuï®
[¿¼ÑÐ] 11408×Ü·Ö309£¬Ò»Ö¾Ô¸¶«ÄÏ´óѧÇóµ÷¼Á£¬²»Ìôרҵ +5 Ì츳´øµ½THU 2026-03-29 6/300 2026-03-30 20:49 by dick_runner
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û