SU146736A1 - Method of regeneration of terephthalic acid diglycolic ester by splitting polyethylene terephthalate - Google Patents

Method of regeneration of terephthalic acid diglycolic ester by splitting polyethylene terephthalate

Info

Publication number
SU146736A1
SU146736A1 SU734892A SU734892A SU146736A1 SU 146736 A1 SU146736 A1 SU 146736A1 SU 734892 A SU734892 A SU 734892A SU 734892 A SU734892 A SU 734892A SU 146736 A1 SU146736 A1 SU 146736A1
Authority
SU
USSR - Soviet Union
Prior art keywords
regeneration
polyethylene terephthalate
splitting
terephthalic acid
ester
Prior art date
Application number
SU734892A
Other languages
Russian (ru)
Inventor
Б
Е.Б. Кремер
В Петухов
Original Assignee
Б
Е.Б. Кремер
В Петухов
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Б, Е.Б. Кремер, В Петухов filed Critical Б
Priority to SU734892A priority Critical patent/SU146736A1/en
Application granted granted Critical
Publication of SU146736A1 publication Critical patent/SU146736A1/en

Links

Description

При производстве полиэфирного волокна и пленок из полиэтилентерефталевой смолы получаетс  большое количество отходов.In the production of polyester fiber and polyethylene terephthalic resin films, a large amount of waste is produced.

Известный способ регенерации дигликолевого эфира терефталевой кислоты из этих отходов обработкой их этиленгликолем запимает 6-9 часов.A known method of regeneration of terephthalic diglycolic ester from these wastes by treating them with ethylene glycol captures 6–9 hours.

Предлагаемый способ ускор ет процесс за счет применени  катализаторов-солей угольной и уксусной кислот.The proposed method accelerates the process by using carbon-acetic acid salt catalysts.

Получаемый дигликолевый эфир терефталевой кислоты путем переэтерификации перевод т в диметилтерефталат, регенериру  свободный этиленгликоль. Выдел емые диметилтерефталат и этиленгликоль вновь используют в качестве исходных в синтезе полиэтилентерефталата. Пример.The resulting terephthalic acid diglycol ester is converted into dimethyl terephthalate by transesterification, regenerated with free ethylene glycol. The recovered dimethyl terephthalate and ethylene glycol are again used as starting materials in the synthesis of polyethylene terephthalate. Example.

Берут 12 отдельных проб, состо щих из 100 вес. ч. полиэтилентерефталевой крошки, 300 вес. ч. этиленгликол  с добавками (вес. ч.):Take 12 separate samples consisting of 100 weight. including polyethylene terephthalic chips, 300 wt. including ethylene glycol with additives (wt. h):

в пробе № 1 -0,3 карбоната свинцаin sample number 1-0.3 carbonate lead

в пробе № 2 -1,0 карбоната магни in sample number 2 -1,0 magnesium carbonate

в пробе № 3 -1,0 карбоната кали in sample number 3 -1,0 potassium carbonate

в пробе № 4 -1,0 карбоната натри in sample number 4 -1.0 sodium carbonate

в пробе № 5 -0,15 карбоната марганцаin sample number 5-0.15 manganese carbonate

в пробе № 6 -0,7 карбоната никел in sample number 6-0.7 nickel carbonate

в пробе № 7 -0,05 карбоната цинкаin the sample number 7-0.05 zinc carbonate

в пробе № 8 -0,4 карбоната кобальтаin sample number 8 -0.4 cobalt carbonate

в пробе JY 9 -0,3 ацетата марганцаin the sample JY 9-0.3 manganese acetate

в пробе № 10-0,4 ацетата кобальтаin the sample number 10-0,4 cobalt acetate

в пробе Л9 И-0,4 ацетата магни in the sample L9 And 0.4 mg magnesium acetate

в пробе № 12-0,1 ацетата цинкаin the sample number 12-0,1 zinc acetate

Пробы нагревают при 197,4° в сосудах, снабженных обратными холодильниками . Растворение проб № 1, 2, 3, 4, 5, 6, 8, 10 заканчиваетс  через 2 часа, пробы N° 7, 9, 11 и 12 раствор ютс  через один час.Samples are heated at 197.4 ° in vessels equipped with reflux condensers. Dissolution of samples No. 1, 2, 3, 4, 5, 6, 8, 10 ends after 2 hours, samples N ° 7, 9, 11 and 12 dissolve after one hour.

№ 146736-2 Из полученных растворов дигликолевого эфира терафталевой кислоты путем переэтерификации метанолом получают диметилтерефталат и регенерируют этиленгликоль, которые пригодны дл  синтеза полиэтилентерефталата. Температура плавлени  регенерированного диметилтерефталата лежит в пределах 140,3-140,6°.No. 146736-2 From the obtained solutions of teraphthalic acid diglycol ether, by transesterification with methanol, dimethyl terephthalate is obtained and ethylene glycol is regenerated, which are suitable for the synthesis of polyethylene terephthalate. The melting point of regenerated dimethyl terephthalate is in the range of 140.3-140.6 °.

Предмет изобретени Subject invention

Способ регенерации дигликолевого эфира терефталевой кислоты расщеплением полиэтилентерефталата этиленгликолем, отличающийс  тем, что, с целью сокращени  продолжительности процесса, его ведут в присутствии катализаторов - солей угольной и уксусной кислот.The method of regeneration of terephthalic acid diglycolic ester by splitting polyethylene terephthalate with ethylene glycol, characterized in that, in order to reduce the duration of the process, it is carried out in the presence of catalysts - salts of carbonic and acetic acids.

SU734892A 1961-06-19 1961-06-19 Method of regeneration of terephthalic acid diglycolic ester by splitting polyethylene terephthalate SU146736A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU734892A SU146736A1 (en) 1961-06-19 1961-06-19 Method of regeneration of terephthalic acid diglycolic ester by splitting polyethylene terephthalate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU734892A SU146736A1 (en) 1961-06-19 1961-06-19 Method of regeneration of terephthalic acid diglycolic ester by splitting polyethylene terephthalate

Publications (1)

Publication Number Publication Date
SU146736A1 true SU146736A1 (en) 1961-11-30

Family

ID=48302167

Family Applications (1)

Application Number Title Priority Date Filing Date
SU734892A SU146736A1 (en) 1961-06-19 1961-06-19 Method of regeneration of terephthalic acid diglycolic ester by splitting polyethylene terephthalate

Country Status (1)

Country Link
SU (1) SU146736A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022243832A1 (en) * 2021-05-17 2022-11-24 Aquafil S.P.A. Process for depolymerizing polyethylene terephthalate by glycolysis

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022243832A1 (en) * 2021-05-17 2022-11-24 Aquafil S.P.A. Process for depolymerizing polyethylene terephthalate by glycolysis

Similar Documents

Publication Publication Date Title
US4011251A (en) Method of preparing esters of glycerol and polyglycerols and C5-C9 monocarboxylic fatty acids
DE1034623B (en) Process for the preparation of vinyl ether esters of saturated monocarboxylic acids
NO120009B (en)
US3594414A (en) Process for the preparation of fiber-grade terephthalic acid
CN103360260B (en) Preparation technology of ethylene glycol terephthalate and preparation method of polyester
GB1298929A (en) A process for the production of allyl alcohol
SU146736A1 (en) Method of regeneration of terephthalic acid diglycolic ester by splitting polyethylene terephthalate
ES441560A1 (en) Separation of acids and esters in the processing of waste salt solution of cyclohexanone manufacture
SU412182A1 (en)
KR900701724A (en) Recovery of Dialkyl Naphthalene-2,6-Dicarboxylate from Naphthalene-2,6-Dicarboxylic Acid-Containing Polyester
DE1543958A1 (en) Process for the preparation of cyclic ester anhydrides of alpha-hydroxycarboxylic acids
SU1088662A3 (en) Process for preparing dimethyltherephthalate
GB822834A (en) A method of processing waste of polyethylene terephthalate by hydrolysis
CN110862520A (en) Method for preparing PET (polyethylene terephthalate) by using terephthalic acid in alkali-minimization wastewater
DE3103136A1 (en) Novel bicyclic ether carbonates, process for their preparation, and their use
US2418237A (en) Process for preparation of 2, 2-dialkyl-1, 3-propanediamines
US2847464A (en) Preparation of lactic acid
DE938787C (en) Process for the preparation of esters and / or polyesters from 8-oxytricyclodecene-4
SU443024A1 (en) Method for producing carboxylic esters
SU63113A1 (en) The method of producing acetyls of polyvinyl alcohol
SU122148A3 (en) The method of obtaining terephthalic acid
DE2511807C3 (en) Process for the production of esters of polyhydric alcohols and monocarboxylic fatty acids with 5 to 9 carbon atoms
DE1543687C3 (en) Process for the preparation of a mixture of 6- and 7-carboxy-2-hydroxymethyl-1,4-benzodioxane
JPS58122903A (en) Production of ethylene/vinyl acetate copolymer saponificate
US2617814A (en) Methods of extracting fatty matters from cork