WO1996026970A1 - Byproduct stream purification in the preparation of 1,3-propanediol-based polyesters - Google Patents
Byproduct stream purification in the preparation of 1,3-propanediol-based polyesters Download PDFInfo
- Publication number
- WO1996026970A1 WO1996026970A1 PCT/EP1996/000809 EP9600809W WO9626970A1 WO 1996026970 A1 WO1996026970 A1 WO 1996026970A1 EP 9600809 W EP9600809 W EP 9600809W WO 9626970 A1 WO9626970 A1 WO 9626970A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- acrolein
- solution
- aqueous
- byproduct
- propanediol
- Prior art date
Links
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
-
- 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
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
- C08G63/181—Acids containing aromatic rings
- C08G63/183—Terephthalic acids
-
- 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
- C08G63/88—Post-polymerisation treatment
- C08G63/90—Purification; Drying
Definitions
- This invention relates to the preparation of poly(propylene terephthalate) ("PPT") and related copolyesters.
- PPT poly(propylene terephthalate)
- the invention relates to the treatment of a byproduct-containing stream in a PPT preparation process.
- PPT poly(ethylene glycol)
- PDO 1, 3-propanediol
- This object is achieved by base treatment of the aqueous byproduct stream, optionally followed by biotreatment thereof.
- the present invention therefore provides a process for preparing a 1, 3-propanediol-based polyester, comprising contacting an aqueous stream containing acrolein byproduct with a base for a time effective to reduce the acrolein content of the aqueous stream.
- the invention provides in a process in which at least one dicarboxylic acid and 1,3-propane- diol are contacted at elevated temperature to produce an aqueous product mixture comprising a 1, 3-propanediol- based polyester and an aqueous solution of acrolein, the improvement which comprises:
- the process of the invention provides a byproduct stream containing reduced levels of acrolein.
- the invention process involves forming a basic aqueous solution of the acrolein byproduct of the condensation polymerization of 1, 3-propanediol and at least one dicarboxylic acid to prepare a 1,3-propane- diol-based polyester.
- the polyester reaction product mixture can contain one or more additional diols such as ethylene glycol, 1, 4-butanediol, 1, -cyclohexane dimethanol and neopentyl glycol.
- Suitable dicarboxylic acids include, for example, terephthalic acid, isophthalic acid and 2 , 6-naphthalene dicarboxylic acid.
- the polyester and copolyester condensation products of such diol and diacid monomers are referred to herein as 1, 3-propanediol-based polyesters or PDO-based polyesters.
- Water-soluble byproducts are found in the aqueous stream distilled from the PDO-based polyester reaction product mixture.
- the amount of typical byproducts in the aqueous distillate will generally be within the range of about 100 to about 2500 ppm acrolein, 0.1 to 5 weight percent allyl alcohol and 0.1 to 10 weight percent PDO, based on the weight of the distillate.
- the invention process involves addition of a base to the aqueous byproduct solution.
- the base is preferably an inorganic base, most preferably selected from alkali and alkaline earth metal hydroxides, including lithium hydroxide, sodium hydroxide, potassium hydroxide, magnesium hydroxide and calcium hydroxide, and the corresponding carbonates and bicarbonates.
- the preferred base because of its cost and effectiveness, is sodium hydroxide.
- the amount of base added to the aqueous byproduct solution is that which is sufficient to impart a pH (at 25 °C) of the aqueous solution of greater than 7.5, preferably greater than 8, most preferably greater than 10.
- the amount added will typically be such that the weight ratio of base:acrolein is within the range of 0.01 to 20, preferably 0.1 to 10, most preferably 0.2 to 5.
- the preferred amount of base will be up to 2.5% by weight based on the total weight of the aqueous solution, although higher levels of base can be used if desired for faster reaction and if not detrimental to subsequent biotreatment.
- the temperature during the base treatment can affect the rate of disappearance of the acrolein and will generally be within the range of 0 to 50 °C, preferably from 10 to 40 °C. Temperatures above 50 °C, i.e., near or above the boiling point of acrolein, are effective but generally to be avoided since this will increase the evaporation of acrolein. The process is effective at temperatures le'ss than 0 °C, but treatment times may be prolonged.
- the aqueous stream is held in a vessel such as a tank or pipe for a length of time to allow the acrolein to react with the base.
- the time will typically be from a few minutes to several days and will depend on the amount of base, the temperature, the initial concentration of acrolein and the final concentration of acrolein desired. Generally, treatment times will fall within the range of 1 to about 100 hours.
- the solution may be optionally diluted with additional aqueous fluid such as a second aqueous byproduct stream.
- the treated aqueous solution can optionally be passed to a biotreatment process.
- Biotreatment will generally involve contact with activated sludge in an aeration basin at a temperature within the range of 1 to 40 °C, a dissolved oxygen content within the range of 0.5 to 8 mg/1, and a typical dilution ratio of 10-500:1. It is preferred that treatment with base combined with optional dilution be carried out so as to reduce the concentration of acrolein to less than 3 ppm, most preferably to less than 0.3 ppm, prior to any biotreatment. Other treatment methods such as reverse osmosis, ultrafiltration and adsorption may be used in combination with the invention process.
- PPT byproduct solution (76.6427 g) was spiked with 0.1247 g acrolein (97%) to bring the acrolein level to about 1950 ppm by GC analysis.
- Two samples of this water in screw cap vials were treated with caustic.
- 0.0980 g of IN sodium hydroxide was added to 10.380 g of the ' solution.
- 0.2341 g of IN sodium hydroxide was added to 10.380 g of the solution.
- the vials were sealed and allowed to stand at room temperature.
- the vials were sampled periodically and analyzed by gas chromatography using clean dioxane as a diluent and tetrahydrofuran as an internal standard. The results are shown in Table 1.
- a simulated PPT byproduct mixture was prepared by mixing together 0.4809 g allyl alcohol, 2.6063 g
- PPT byproduct solution (70.428 g) was spiked with 0.1690 g acrolein to bring the acrolein level to about 2630 ppm by GC analysis and 6.58 g was transferred to a screw cap vial.
- To the remaining solution was added approximately 0.3 g IN sodium hydroxide solution to give a final solution of 64.24 g with a pH of about 10 (sample E) .
- Ethylene glycol was added to portions of sample E to make sample F with about 1.1% ethylene glycol and sample G with about 10% ethylene glycol.
- the sealed samples were allowed to stand at room temperature and were analyzed by GC. The results are shown in Table 2.
- PPT byproduct solution 53.1842 g was spiked with 0.090 g acrolein to bring the acrolein level to about 2610 ppm.
- Three samples were prepared from this solution.
- Sample H containing 10.1576 g byproduct solution with 0.512 g 0.1N hydrochloric acid (final pH 3) .
- Sample I contained 9.5485 g by product solution with 0.5212 g 0.1N HC1 and 0.1063 g ethylene glycol.
- Sample J contained 9.4565 g byproduct solution with 0.4976 g 0.IN HC1 and 0.5092 g ethylene glycol.
- the sealed vials were allowed to stand at room temperature and analyzed by GC. Results are shown in Table 3. The acid treatment, with or without added glycol, had relatively little effect on the concentration of acrolein.
- a simulated PPT byproduct solution was prepared by mixing together 0.41 g allyl alcohol, 2.75 g 1,3-propanediol and 0.052 g acrolein and diluting with 51.69 g distilled water.
- the solution was cooled to about 1 °C.
- Samples of the solution in screw cap vials were tested with caustic.
- 0.12 g IN NaOH was mixed with 10.304 g of solution.
- sample L 0.266 g IN NaOH was mixed with 9.760 g of solution.
- Sample M 0.504 g IN NaOH was mixed with 9.989 g of solution.
- the vials were capped and stored at about 1 °C in a refrigerator. Results are shown in Table 4. TABLE 4
- the oxygen utilization rate is a direct measurement of the microbial consumption rate of the waste materials.
- the activated sludge was taken from a chemical manufacturing plant where polyester (PET) based on ethylene glycol is produced.
- PET polyester
- a byproduct solution from the synthesis of polypropylene terephthalate (PPT) containing 1000 ppm acrolein was treated with sodium hydroxide as described above in Example 2 and used as a feed.
- the byproduct solution from the PET plant was used as a standard feed for comparison.
- Acrolein was added at various levels to the PET solution to show whether it had any adverse effect on oxygen uptake rates.
- Table 5 Oxygen uptake rates are in millilitres of oxygen at 20 °C and atmospheric (100 kPa) pressure.
- the PPT solution treated with caustic did not affect the oxygen uptake rate, while 5 to 15 ppm of acrolein reduced the rate by 29-52% in 12 hours and 34-65% in 28 hours. These results indicate that the caustic treatment removed the inhibitory effect of the acrolein in the PPT byproduct solution and that the organic products formed in the caustic treatment were nontoxic to the biomass.
- COD Chemical Oxygen Demand Millimetres O2 at 20 °C, 1 atm.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyesters Or Polycarbonates (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP96905815A EP0812337B1 (en) | 1995-02-27 | 1996-02-26 | Byproduct stream purification in the preparation of 1,3-propanediol-based polyesters |
CA002213745A CA2213745C (en) | 1995-02-27 | 1996-02-26 | Byproduct stream purification in the preparation of 1,3-propanediol-based polyesters |
DE69601165T DE69601165T2 (en) | 1995-02-27 | 1996-02-26 | BY-PRODUCT CLEANING IN THE PRODUCTION OF POLYESTERS BASED ON 1,3-PROPANDIOL |
PL96321965A PL321965A1 (en) | 1995-02-27 | 1996-02-26 | Method purifying a stream of a by-product obtained in production of 1,3-propanodiole baseed polyesters |
AU49427/96A AU689378B2 (en) | 1995-02-27 | 1996-02-26 | Byproduct stream purification in the preparation of 1,3-propanediol-based polyesters |
JP52601796A JP3415848B2 (en) | 1995-02-27 | 1996-02-26 | Purification of by-product streams in the production of 1,3-propanediol-based polyethers |
BR9607389A BR9607389A (en) | 1995-02-27 | 1996-02-26 | Purification of by-product stream in the preparation of polyesters based on 1,3 propanediol |
MXPA/A/1997/006480A MXPA97006480A (en) | 1995-02-27 | 1997-08-25 | Purification of a sub-product current in the preparation of base polyesters of 1.3-propand |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US395,231 | 1995-02-27 | ||
US08/395,231 US5459229A (en) | 1995-02-27 | 1995-02-27 | By product stream purification in the preparation of 1,3-propanediol-based polyesters |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996026970A1 true WO1996026970A1 (en) | 1996-09-06 |
Family
ID=23562194
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1996/000809 WO1996026970A1 (en) | 1995-02-27 | 1996-02-26 | Byproduct stream purification in the preparation of 1,3-propanediol-based polyesters |
Country Status (17)
Country | Link |
---|---|
US (1) | US5459229A (en) |
EP (1) | EP0812337B1 (en) |
JP (1) | JP3415848B2 (en) |
KR (1) | KR100398820B1 (en) |
CN (1) | CN1074428C (en) |
AR (1) | AR001015A1 (en) |
AT (1) | ATE174608T1 (en) |
AU (1) | AU689378B2 (en) |
BR (1) | BR9607389A (en) |
DE (1) | DE69601165T2 (en) |
ES (1) | ES2125718T3 (en) |
MY (1) | MY113798A (en) |
PL (1) | PL321965A1 (en) |
TR (1) | TR199700855T1 (en) |
TW (1) | TW376393B (en) |
WO (1) | WO1996026970A1 (en) |
ZA (1) | ZA961511B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002008310A2 (en) * | 2000-07-20 | 2002-01-31 | Shell Internationale Research Maatschappij B.V. | Process for producing polytrimethylene terephthalate |
Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5527973A (en) * | 1994-12-16 | 1996-06-18 | Kelsey; Donald R. | Purification of 1,3-propanediol |
DE19705249A1 (en) * | 1997-02-12 | 1998-08-13 | Zimmer Ag | Process for the production of polypropylene terephthalate |
MY118950A (en) * | 1997-04-30 | 2005-02-28 | Shell Int Research | Purification of by- product stream in preparation of polytrimethylene terephthalate |
US6245844B1 (en) * | 1998-09-18 | 2001-06-12 | E. I. Du Pont De Nemours And Company | Nucleating agent for polyesters |
US6245879B1 (en) * | 1999-01-29 | 2001-06-12 | Shell Oil Company | Purification of 1,3-propanediol in carbonyl-containing stream |
US5989665A (en) * | 1999-03-15 | 1999-11-23 | Eastman Chemical Company | Copolyesters of 1,3-propanediol having improved gas barrier properties |
US6350895B1 (en) | 1999-03-26 | 2002-02-26 | E. I. Du Pont De Nemours And Company | Transesterification process using yttrium and samarium compound catalystis |
US6331264B1 (en) | 1999-03-31 | 2001-12-18 | E. I. Du Pont De Nemours And Company | Low emission polymer compositions |
US6277947B1 (en) | 2000-04-21 | 2001-08-21 | Shell Oil Company | Process of producing polytrimethylene terephthalate (PTT) |
US6512080B2 (en) | 1999-04-22 | 2003-01-28 | Shell Oil Company | Process of producing polytrimethylene terephthalate (PTT) |
ATE234336T1 (en) * | 1999-04-22 | 2003-03-15 | Zimmer Ag | METHOD FOR PRODUCING POLYTRIMETHYLENE TEREPHTHALATE (PTT) |
US6277289B1 (en) | 1999-07-01 | 2001-08-21 | E. I. Du Pont De Nemours And Company | Treatment of aqueous aldehyde waste streams |
US6284930B1 (en) | 1999-07-30 | 2001-09-04 | E.I. Du Pont De Nemours And Company | Process for the preparation of 3-hydroxypropanal |
MXPA02001942A (en) | 1999-08-25 | 2002-10-31 | Du Pont | Preparation of poly(trimethylene terephthalate) with low level of di(1,3 propylene glycol). |
US6436503B1 (en) | 1999-09-08 | 2002-08-20 | General Electric Company | Data storage medium containing polyestercarbonate |
US6410619B2 (en) | 1999-11-22 | 2002-06-25 | Bayer Corporation | Method for conditioning organic pigments |
ES2219377T5 (en) * | 2000-02-11 | 2010-10-14 | E.I. Du Pont De Nemours And Company | CONTINUOUS POLI PRODUCTION PROCEDURE (TRIMETHYLENE TEREFTALATE). |
US6353062B1 (en) | 2000-02-11 | 2002-03-05 | E. I. Du Pont De Nemours And Company | Continuous process for producing poly(trimethylene terephthalate) |
US6528579B2 (en) | 2000-02-17 | 2003-03-04 | Shell Oil Company | Zero-heel polyester process |
GB2361925A (en) | 2000-05-02 | 2001-11-07 | Shell Internat Res Maatschhapp | High temperature solid state polymerisation of poly(trimethylene terephthalate) |
US6403762B1 (en) | 2000-08-21 | 2002-06-11 | Shell Oil Company | Solid state polymerization process for poly(trimethylene terephthalate) utilizing a combined crystallization/preheating step |
US6600061B1 (en) | 2000-11-15 | 2003-07-29 | General Electric Company | Method for the continuous production of aromatic carbonates |
DE10125677B4 (en) * | 2001-05-25 | 2013-05-16 | Lurgi Zimmer Gmbh | Process and apparatus for the preparation of polytrimethylene terephthalate |
EP1347005A1 (en) * | 2002-03-23 | 2003-09-24 | Zimmer AG | Polytrimethylene terephtalate resins with improved properties |
US20040222154A1 (en) * | 2003-05-08 | 2004-11-11 | E.I.Du Pont De Nemours & Company | Treatment of non-aqueous aldehyde waste streams |
DE102005017428A1 (en) * | 2005-04-15 | 2006-10-19 | Zimmer Ag | Preparing polyoxytrimethyleneglycol/polytrimethyleneterephthalate/polyoxytrimethyleneglycol units comprises esterification, precondensation and polycondensation of terephthalic acid and its derivative with propandiol and purifying |
US20070149756A1 (en) * | 2005-12-26 | 2007-06-28 | Futura Polyesters Limited | Compositions and methods of manufacturing polytrimethylene naphthalate |
CN104987497A (en) * | 2015-07-20 | 2015-10-21 | 福建师范大学泉港石化研究院 | Method for removing acid value in polyester polyol by column chromatography separation |
Citations (1)
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EP0547553A1 (en) * | 1991-12-18 | 1993-06-23 | Hoechst Celanese Corporation | Poly(1,3-propylene terephthalate) |
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US4096122A (en) * | 1972-03-18 | 1978-06-20 | Dynamit Nobel Aktiengesellschaft | Process for the production of polyesters of 1,4-butanediol |
US4014858A (en) * | 1975-05-12 | 1977-03-29 | Standard Oil Company | Polybutylene terephthalate |
US4375538A (en) * | 1980-12-22 | 1983-03-01 | Monsanto Company | Polymer compositions comprising adducts of acrolein and isocyanuric acid |
US4611049A (en) * | 1984-06-07 | 1986-09-09 | Teijin Limited | Process for producing aromatic polyester |
DE3422733A1 (en) * | 1984-06-19 | 1985-12-19 | Teijin Ltd., Osaka | Process for the preparation of aromatic polyesters |
JP2976500B2 (en) * | 1990-08-27 | 1999-11-10 | 東洋紡績株式会社 | Resin particles and method for producing the same |
JP2758525B2 (en) * | 1992-02-12 | 1998-05-28 | ポリプラスチックス株式会社 | Modified polyester |
-
1995
- 1995-02-27 US US08/395,231 patent/US5459229A/en not_active Expired - Lifetime
-
1996
- 1996-02-16 MY MYPI96000596A patent/MY113798A/en unknown
- 1996-02-23 AR ARP960101493A patent/AR001015A1/en unknown
- 1996-02-26 AU AU49427/96A patent/AU689378B2/en not_active Ceased
- 1996-02-26 TR TR97/00855T patent/TR199700855T1/en unknown
- 1996-02-26 JP JP52601796A patent/JP3415848B2/en not_active Expired - Fee Related
- 1996-02-26 PL PL96321965A patent/PL321965A1/en unknown
- 1996-02-26 ZA ZA961511A patent/ZA961511B/en unknown
- 1996-02-26 EP EP96905815A patent/EP0812337B1/en not_active Revoked
- 1996-02-26 CN CN96192183A patent/CN1074428C/en not_active Expired - Fee Related
- 1996-02-26 AT AT96905815T patent/ATE174608T1/en not_active IP Right Cessation
- 1996-02-26 ES ES96905815T patent/ES2125718T3/en not_active Expired - Lifetime
- 1996-02-26 BR BR9607389A patent/BR9607389A/en not_active Application Discontinuation
- 1996-02-26 KR KR1019970705888A patent/KR100398820B1/en not_active IP Right Cessation
- 1996-02-26 WO PCT/EP1996/000809 patent/WO1996026970A1/en not_active Application Discontinuation
- 1996-02-26 DE DE69601165T patent/DE69601165T2/en not_active Revoked
- 1996-03-06 TW TW085102736A patent/TW376393B/en not_active IP Right Cessation
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
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EP0547553A1 (en) * | 1991-12-18 | 1993-06-23 | Hoechst Celanese Corporation | Poly(1,3-propylene terephthalate) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002008310A2 (en) * | 2000-07-20 | 2002-01-31 | Shell Internationale Research Maatschappij B.V. | Process for producing polytrimethylene terephthalate |
WO2002008310A3 (en) * | 2000-07-20 | 2002-08-15 | Shell Int Research | Process for producing polytrimethylene terephthalate |
US6576774B2 (en) | 2000-07-20 | 2003-06-10 | Shell Oil Company | Process for recycling polytrimethylene terephthalate cyclic dimer |
KR100733642B1 (en) * | 2000-07-20 | 2007-06-28 | 셀 인터나쵸나아레 레사아치 마아츠샤피 비이부이 | Process for producing polytrimethylene terephthalate |
Also Published As
Publication number | Publication date |
---|---|
JP3415848B2 (en) | 2003-06-09 |
AR001015A1 (en) | 1997-08-27 |
MX9706480A (en) | 1997-11-29 |
JPH11501060A (en) | 1999-01-26 |
BR9607389A (en) | 1997-11-25 |
KR19980702488A (en) | 1998-07-15 |
US5459229A (en) | 1995-10-17 |
TR199700855T1 (en) | 1998-02-21 |
PL321965A1 (en) | 1998-01-05 |
AU4942796A (en) | 1996-09-18 |
CN1178539A (en) | 1998-04-08 |
KR100398820B1 (en) | 2004-02-05 |
MY113798A (en) | 2002-05-31 |
DE69601165T2 (en) | 1999-06-10 |
DE69601165D1 (en) | 1999-01-28 |
EP0812337A1 (en) | 1997-12-17 |
ES2125718T3 (en) | 1999-03-01 |
EP0812337B1 (en) | 1998-12-16 |
CN1074428C (en) | 2001-11-07 |
TW376393B (en) | 1999-12-11 |
ZA961511B (en) | 1996-09-03 |
ATE174608T1 (en) | 1999-01-15 |
AU689378B2 (en) | 1998-03-26 |
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