ZA200309310B - Method for increasing solid state polymerization rate. - Google Patents
Method for increasing solid state polymerization rate. Download PDFInfo
- Publication number
- ZA200309310B ZA200309310B ZA200309310A ZA200309310A ZA200309310B ZA 200309310 B ZA200309310 B ZA 200309310B ZA 200309310 A ZA200309310 A ZA 200309310A ZA 200309310 A ZA200309310 A ZA 200309310A ZA 200309310 B ZA200309310 B ZA 200309310B
- Authority
- ZA
- South Africa
- Prior art keywords
- particles
- mass
- temperature
- range
- inert gas
- Prior art date
Links
- 238000006116 polymerization reaction Methods 0.000 title claims description 38
- 239000007787 solid Substances 0.000 title claims description 36
- 238000000034 method Methods 0.000 title claims description 32
- 239000002245 particle Substances 0.000 claims description 59
- 229920000728 polyester Polymers 0.000 claims description 41
- 238000002425 crystallisation Methods 0.000 claims description 22
- 230000008025 crystallization Effects 0.000 claims description 22
- 239000011261 inert gas Substances 0.000 claims description 15
- 229920001730 Moisture cure polyurethane Polymers 0.000 claims description 11
- 239000007789 gas Substances 0.000 claims description 6
- 238000012546 transfer Methods 0.000 claims description 6
- 230000000379 polymerizing effect Effects 0.000 claims description 3
- -1 polyethylene terephthalate Polymers 0.000 description 29
- 239000008188 pellet Substances 0.000 description 25
- 229920000139 polyethylene terephthalate Polymers 0.000 description 23
- 239000005020 polyethylene terephthalate Substances 0.000 description 22
- 229920000642 polymer Polymers 0.000 description 19
- 125000004432 carbon atom Chemical group C* 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 12
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 12
- 150000005690 diesters Chemical class 0.000 description 11
- 230000004927 fusion Effects 0.000 description 9
- 238000002474 experimental method Methods 0.000 description 8
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 150000002334 glycols Chemical class 0.000 description 5
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 150000002009 diols Chemical class 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 230000000875 corresponding effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- 229940043375 1,5-pentanediol Drugs 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- FQXGHZNSUOHCLO-UHFFFAOYSA-N 2,2,4,4-tetramethyl-1,3-cyclobutanediol Chemical compound CC1(C)C(O)C(C)(C)C1O FQXGHZNSUOHCLO-UHFFFAOYSA-N 0.000 description 1
- GZZLQUBMUXEOBE-UHFFFAOYSA-N 2,2,4-trimethylhexane-1,6-diol Chemical compound OCCC(C)CC(C)(C)CO GZZLQUBMUXEOBE-UHFFFAOYSA-N 0.000 description 1
- DSKYSDCYIODJPC-UHFFFAOYSA-N 2-butyl-2-ethylpropane-1,3-diol Chemical compound CCCCC(CC)(CO)CO DSKYSDCYIODJPC-UHFFFAOYSA-N 0.000 description 1
- QNKRHLZUPSSIPN-UHFFFAOYSA-N 2-ethyl-2-(2-methylpropyl)propane-1,3-diol Chemical compound CCC(CO)(CO)CC(C)C QNKRHLZUPSSIPN-UHFFFAOYSA-N 0.000 description 1
- 101100369915 Drosophila melanogaster stas gene Proteins 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 101150003530 Tsnax gene Proteins 0.000 description 1
- LUSFFPXRDZKBMF-UHFFFAOYSA-N [3-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCCC(CO)C1 LUSFFPXRDZKBMF-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000019437 butane-1,3-diol Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- JLVWYWVLMFVCDI-UHFFFAOYSA-N diethyl benzene-1,3-dicarboxylate Chemical compound CCOC(=O)C1=CC=CC(C(=O)OCC)=C1 JLVWYWVLMFVCDI-UHFFFAOYSA-N 0.000 description 1
- ONIHPYYWNBVMID-UHFFFAOYSA-N diethyl benzene-1,4-dicarboxylate Chemical compound CCOC(=O)C1=CC=C(C(=O)OCC)C=C1 ONIHPYYWNBVMID-UHFFFAOYSA-N 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- OVPXRLUTUWRYEY-UHFFFAOYSA-N dimethyl naphthalene-1,8-dicarboxylate Chemical compound C1=CC(C(=O)OC)=C2C(C(=O)OC)=CC=CC2=C1 OVPXRLUTUWRYEY-UHFFFAOYSA-N 0.000 description 1
- 238000011143 downstream manufacturing Methods 0.000 description 1
- 238000002635 electroconvulsive therapy Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 229920002215 polytrimethylene terephthalate Polymers 0.000 description 1
- XRVCFZPJAHWYTB-UHFFFAOYSA-N prenderol Chemical compound CCC(CC)(CO)CO XRVCFZPJAHWYTB-UHFFFAOYSA-N 0.000 description 1
- 229950006800 prenderol Drugs 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/78—Preparation processes
- C08G63/80—Solid-state polycondensation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B9/00—Making granules
- B29B9/16—Auxiliary treatment of granules
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B9/00—Making granules
- B29B9/16—Auxiliary treatment of granules
- B29B2009/165—Crystallizing granules
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Polyesters Or Polycarbonates (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/927,654 US6451966B1 (en) | 2001-08-10 | 2001-08-10 | Method for increasing solid state polymerization rate |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200309310B true ZA200309310B (en) | 2004-11-29 |
Family
ID=25455052
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200309310A ZA200309310B (en) | 2001-08-10 | 2003-11-28 | Method for increasing solid state polymerization rate. |
Country Status (20)
Country | Link |
---|---|
US (1) | US6451966B1 (xx) |
EP (1) | EP1414885B8 (xx) |
JP (1) | JP4094547B2 (xx) |
KR (1) | KR100829341B1 (xx) |
CN (1) | CN1235937C (xx) |
AR (1) | AR035092A1 (xx) |
AT (1) | ATE377617T1 (xx) |
BR (1) | BR0211012B1 (xx) |
CA (1) | CA2453906A1 (xx) |
CZ (1) | CZ300097B6 (xx) |
DE (1) | DE60223383T2 (xx) |
DZ (1) | DZ3274A1 (xx) |
EA (1) | EA005177B1 (xx) |
EG (1) | EG23316A (xx) |
ES (1) | ES2295394T3 (xx) |
MX (1) | MXPA03011513A (xx) |
PL (1) | PL366872A1 (xx) |
TW (1) | TWI229098B (xx) |
WO (1) | WO2003014185A1 (xx) |
ZA (1) | ZA200309310B (xx) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100406493C (zh) * | 2003-02-28 | 2008-07-30 | 三菱化学株式会社 | 聚酯树脂粉末的制法及聚酯预成型料坯的制法及聚酯树脂粉末的热处理用装置 |
US7250486B1 (en) | 2004-12-15 | 2007-07-31 | Uop Llc | Method and apparatus for crystallizing polymer particles |
US20100222543A1 (en) * | 2005-08-22 | 2010-09-02 | Reliance Industries Ltd | Process for the production of slow crystallizing polyester resin |
EP1939238B1 (en) | 2005-09-01 | 2010-10-20 | Mitsubishi Chemical Corporation | Apparatus for heat treatment of polyester particle and method of multistage solid-phase polycondensation of polyester particle |
BRPI0615322A2 (pt) | 2005-09-01 | 2012-12-04 | Mitsubishi Chem Corp | métodos de produção de um poliéster, e de um tereftalato de polietileno |
WO2008075373A2 (en) * | 2006-12-19 | 2008-06-26 | Reliance Industries Ltd. | An efficient process for the production of polyester |
DE102009009957A1 (de) * | 2009-02-23 | 2010-08-26 | Bühler AG | Verfahren zur Herstellung von Polyesterpartikeln bei hohem Durchsatz in einer Linie |
US10167363B2 (en) * | 2014-08-05 | 2019-01-01 | Ester Industries Limited | Modified polybutylene naphthalate for improved performance and process of making thereof |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3405098A (en) | 1965-10-29 | 1968-10-08 | Du Pont | Process for preparing high viscosity linear condensation polyesters from partially polymerized glycol terephthalates |
US3544525A (en) | 1968-03-26 | 1970-12-01 | Allied Chem | Process for crystallization,drying and solid-state polymerization of polyesters |
DE2559290B2 (de) | 1975-12-31 | 1979-08-02 | Davy International Ag, 6000 Frankfurt | Verfahren zur kontinuierlichen Herstellung von hochmolekularem PoIyäthylenterephthalat |
US4165420A (en) | 1977-11-10 | 1979-08-21 | The Goodyear Tire & Rubber Company | Solid state polymerization of polyester prepolymer |
US4271287A (en) | 1979-09-28 | 1981-06-02 | Rohm And Haas Company | Process for the continuous polymerization of polyethylene terephthalate in the solid phase |
US4254253A (en) | 1980-02-21 | 1981-03-03 | The Goodyear Tire & Rubber Company | Preparation of high molecular weight polyester |
US4374975A (en) | 1982-02-02 | 1983-02-22 | The Goodyear Tire & Rubber Company | Process for the production of high molecular weight polyester |
US5633018A (en) | 1995-01-20 | 1997-05-27 | E. I. Du Pont De Nemours And Company | Apparatus for forming crystalline polymer pellets |
US5540868A (en) | 1995-01-20 | 1996-07-30 | E. I. Du Pont De Nemours And Company | Process for pellet formation from amorphous polyester |
US5510454A (en) | 1995-01-20 | 1996-04-23 | E. I. Du Pont De Nemours And Company | Production of poly(ethylene terephthalate) |
US5714262A (en) | 1995-12-22 | 1998-02-03 | E. I. Du Pont De Nemours And Company | Production of poly(ethylene terephthalate) |
IT1283083B1 (it) | 1996-05-30 | 1998-04-07 | Sinco Eng Spa | Procedimento perfezionato per la produzione di resine poliestere |
-
2001
- 2001-08-10 DZ DZ023274A patent/DZ3274A1/xx active
- 2001-08-10 US US09/927,654 patent/US6451966B1/en not_active Expired - Fee Related
-
2002
- 2002-08-05 JP JP2003519130A patent/JP4094547B2/ja not_active Expired - Fee Related
- 2002-08-05 CN CNB028124006A patent/CN1235937C/zh not_active Expired - Fee Related
- 2002-08-05 WO PCT/US2002/024886 patent/WO2003014185A1/en active IP Right Grant
- 2002-08-05 DE DE60223383T patent/DE60223383T2/de not_active Expired - Lifetime
- 2002-08-05 EP EP02759275A patent/EP1414885B8/en not_active Expired - Lifetime
- 2002-08-05 EA EA200301277A patent/EA005177B1/ru not_active IP Right Cessation
- 2002-08-05 CZ CZ20033439A patent/CZ300097B6/cs not_active IP Right Cessation
- 2002-08-05 KR KR1020037016621A patent/KR100829341B1/ko not_active IP Right Cessation
- 2002-08-05 AT AT02759275T patent/ATE377617T1/de not_active IP Right Cessation
- 2002-08-05 BR BRPI0211012-1A patent/BR0211012B1/pt not_active IP Right Cessation
- 2002-08-05 PL PL02366872A patent/PL366872A1/xx not_active Application Discontinuation
- 2002-08-05 CA CA002453906A patent/CA2453906A1/en not_active Abandoned
- 2002-08-05 MX MXPA03011513A patent/MXPA03011513A/es active IP Right Grant
- 2002-08-05 ES ES02759275T patent/ES2295394T3/es not_active Expired - Lifetime
- 2002-08-07 EG EG2002080878A patent/EG23316A/xx active
- 2002-08-08 AR ARP020103002A patent/AR035092A1/es active IP Right Grant
- 2002-08-09 TW TW091118018A patent/TWI229098B/zh not_active IP Right Cessation
-
2003
- 2003-11-28 ZA ZA200309310A patent/ZA200309310B/en unknown
Also Published As
Publication number | Publication date |
---|---|
DE60223383T2 (de) | 2008-08-28 |
MXPA03011513A (es) | 2004-03-18 |
CZ20033439A3 (cs) | 2004-05-12 |
EP1414885B8 (en) | 2007-12-26 |
EA200301277A1 (ru) | 2004-06-24 |
DZ3274A1 (xx) | 2005-05-14 |
KR100829341B1 (ko) | 2008-05-13 |
EP1414885A1 (en) | 2004-05-06 |
BR0211012B1 (pt) | 2012-06-26 |
BR0211012A (pt) | 2004-08-10 |
CN1235937C (zh) | 2006-01-11 |
EA005177B1 (ru) | 2004-12-30 |
CA2453906A1 (en) | 2003-02-20 |
ATE377617T1 (de) | 2007-11-15 |
EG23316A (en) | 2004-11-30 |
KR20040031705A (ko) | 2004-04-13 |
CZ300097B6 (cs) | 2009-01-28 |
TWI229098B (en) | 2005-03-11 |
WO2003014185A1 (en) | 2003-02-20 |
US6451966B1 (en) | 2002-09-17 |
JP2004537622A (ja) | 2004-12-16 |
CN1518571A (zh) | 2004-08-04 |
PL366872A1 (en) | 2005-02-07 |
ES2295394T3 (es) | 2008-04-16 |
DE60223383D1 (de) | 2007-12-20 |
EP1414885B1 (en) | 2007-11-07 |
JP4094547B2 (ja) | 2008-06-04 |
AR035092A1 (es) | 2004-04-14 |
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