KR20030049627A - Method for producing polymer for toner, ink and coating agent by recycling waste polyester - Google Patents

Method for producing polymer for toner, ink and coating agent by recycling waste polyester Download PDF

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KR20030049627A
KR20030049627A KR1020010079882A KR20010079882A KR20030049627A KR 20030049627 A KR20030049627 A KR 20030049627A KR 1020010079882 A KR1020010079882 A KR 1020010079882A KR 20010079882 A KR20010079882 A KR 20010079882A KR 20030049627 A KR20030049627 A KR 20030049627A
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resin
acid
water
polymer
polyester
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KR1020010079882A
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Korean (ko)
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KR100765744B1 (en
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김도균
김효성
김충길
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김도균
김효성
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Priority to KR1020010079882A priority Critical patent/KR100765744B1/en
Priority to EP02791089A priority patent/EP1468034A4/en
Priority to AU2002366296A priority patent/AU2002366296A1/en
Priority to US10/498,920 priority patent/US7166690B2/en
Priority to PCT/KR2002/002359 priority patent/WO2003051956A1/en
Priority to JP2003552832A priority patent/JP4902102B2/en
Priority to CNB02828156XA priority patent/CN100427523C/en
Publication of KR20030049627A publication Critical patent/KR20030049627A/en
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Publication of KR100765744B1 publication Critical patent/KR100765744B1/en

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/78Preparation processes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J11/00Recovery or working-up of waste materials
    • C08J11/04Recovery or working-up of waste materials of polymers
    • C08J11/06Recovery or working-up of waste materials of polymers without chemical reactions
    • C08J11/08Recovery or working-up of waste materials of polymers without chemical reactions using selective solvents for polymer components
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J11/00Recovery or working-up of waste materials
    • C08J11/04Recovery or working-up of waste materials of polymers
    • C08J11/10Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/02Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L93/00Compositions of natural resins; Compositions of derivatives thereof
    • C08L93/04Rosin
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00Inks
    • C09D11/30Inkjet printing inks
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2207/00Properties characterising the ingredient of the composition
    • C08L2207/20Recycled plastic

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Sustainable Development (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Developing Agents For Electrophotography (AREA)

Abstract

PURPOSE: A polyester resin of high value added for use in an ink jet ink binder and a binder for a toner used in copying machines, printers, electro-photographic devices, printing inks, paints or adhesives is provided by using a recycled waste polyester. CONSTITUTION: The process for preparing polyester polymer resin by using a recycled waste polyester comprises the steps of: (a) carrying out the first depolymerization of polyethylene terephthalate by a solid resin dissolving agent, and then adding a polybasic acid to the dissolved polymer to perform the second depolymerization and addition at the same time; (b) adding a polyhydric alcohol to the product obtained in the step (a) to perform polycondensation in the presence of a tin based catalyst so that a polymer having an acid value of 10 to 150 mgKOH/g, an average molecular weight of 3,000 to 50,000 and a softening point of 70 to 150 deg.C can be formed; (c) neutralizing the polymer obtained in the step (b) which has acid value greater than 20 mgKOH/g with a basic compound and dissolving and diluting it in a water based solvent to obtain a water soluble polyester resin, while forming solid resins from the polymer having acid value les than 15 mgKOH/g.

Description

폐 폴리에스테르를 재활용하여 토너, 잉크 및 코팅제용 중합체 제조방법 및 그 조성물{omitted}Recycling waste polyester to produce polymers for toners, inks and coatings, and compositions thereof

본 발명은 폐폴리에틸렌 데레프탈레이드 (이하 PET로 한다.)를 재활용하여 첨단 신소재용 폴리에스텔 수지조성물을 제조하는 방법에 관한 것이다. 근래 PET가 플라스틱 소재로 섬유, PET병, 필름, 사출성형재로 광범위하게 사용되어 이들의 제조과정 및 사용후에 발생되는 폐기물이 환경문제로 대두될 만큼 다량이나 이들을 재활용하는 양이 극히 제한적이고 또한 단순한 물리적으로만 열 용융처리하여 변형품을 만드는 기술수준이어서 재생품의 품질이 만족스럽지 못하여 재활용하는 양이 극히 제한적이었다. 그래서 이들의 처리에 큰 문제가 되고 있으며 이를 해결할 방법이 간절히 요구되고 있는 실정이다. 더구나 고기능성 소재를 얻기위한 연구 및 제조는 지금까지 이루어지지 않았다. 본 발명자들은 상기의 문제를 해소하기 위하여 예의 연구한 결과 폐PET를 로진 및 로진유도체 석유수지 디시아클로펜타디엔레진으로 해중합하여 다염가산과 부가반응을 시켜서 다가알콜을 가하여 축중합 반응을 일으켜서 원하는 물성의 중합체를 얻음으로 원천기술에의한 화학적인 처리결과로 고부가가치를 갖는 유용한 첨단 제품으로 탄생할 수 있다는 결론에 도달하여 본발명을 완성하였다.The present invention relates to a method for producing a polyester resin composition for advanced new materials by recycling waste polyethylene derephthalate (hereinafter referred to as PET). Recently, PET is widely used as a plastic material, such as fibers, PET bottles, films, and injection molding materials, so that the amount of wastes generated during and after the manufacturing process and the use thereof becomes an environmental problem. It was a technical level of physically hot-melting to make deformations, so the quality of recycled products was not satisfactory, and the amount of recycling was extremely limited. Therefore, it is a big problem in their processing and there is an urgent need for a solution to solve this problem. Moreover, research and manufacture for obtaining high functional materials have not been made until now. The present inventors earnestly researched to solve the above problems, and as a result, depolymerized waste PET into rosin and rosin derivative petroleum resin dicyclopentadiene resin, followed by addition reaction with polyhydrochloric acid to add polyhydric alcohol, resulting in polycondensation reaction, resulting in desired physical properties. The present invention was completed by the conclusion that the result of the chemical treatment by the source technology can be produced as a useful high-tech product with high value by obtaining the polymer of.

(1) (A) 폐폴리에틸렌 테레프탈레이트(이하 PET라 한다.)를 고체수지 용해제로 해중합하고 (B) 다염기산으로 2차 해중합을 동반하는 부가반응 시키는 단계; (2) 단계(1)에서 얻어진 생성물에 다가알콜을 가하여 주석계 촉매사용 축중합 반응을 일으켜서 산가 10∼90mgKOH/g, 중량평균 분자량 3,000∼50,000, 연화점 70∼150℃의 중합체를 제조하는 단계: (3) 단계(2)에서 얻어진 중합체중 산가 20mgKOH/g 이상의 중합체는 염기수용액으로 중화하여 물 또는 수친화성 용제 및 이 용제에 물을 혼합한 용액에 용해시켜 수용성 바인다로 제조하는 단계를 포함하는 폴리에스텔수지조성물을 제조하는 단계.(1) depolymerizing (A) waste polyethylene terephthalate (hereinafter referred to as PET) with a solid resin solubilizer and (B) addition reaction with secondary depolymerization with polybasic acid; (2) adding polyhydric alcohol to the product obtained in step (1) to produce a polycondensation reaction using a tin catalyst to prepare a polymer having an acid value of 10 to 90 mgKOH / g, a weight average molecular weight of 3,000 to 50,000, and a softening point of 70 to 150 ° C. (3) a polymer comprising a polymer having an acid value of 20 mg KOH / g or more in the polymer obtained in step (2), neutralized with a basic aqueous solution, dissolved in a water or water affinity solvent and a solution mixed with water to produce a water-soluble binder. Preparing an ester resin composition.

이들 수지 조성물은 복사기, 프린트, 전자사진용 중합법 토너의 원료인 결착제, 잉크젯 잉크 결착제등으로 사용하고 산가 10mgKOH/g 이하의 수지조성물은 그대로 인쇄잉크, 도료, 접착제, 분쇄법 토너의 결착제로 사용가능한 폴리에스텔수지 제조 방법을 제공한다.These resin compositions are used as binders, inkjet ink binders, etc. as raw materials for photocopier, printing, and electrophotographic polymerization toners, and resin compositions having an acid value of 10 mgKOH / g or less are used as binders for printing inks, paints, adhesives, and grinding toners. Provided is a method for producing a polyester resin which can be used zero.

단계(1) (A)에서 사용될수 있는 PET는 테레프탈산과 에틸렌글리콜로부터 합성된 중합체로서 PET섬유 제조시의 발생된 폐 PET병 성형품등으로부터 기계적으로 분쇄 얻어지는 폐PET칩이고 고체 용해제는 로진 및 로진 유도체, 테르펜계수지, 석유수지 및 그 유도체, 디사이클로펜타디엔 및 그 유도체로 검로진, 우드로진, 탈로진, 수첨로진, 마레인화로진, 로진에스텔, 피넨수지, 디펜텐 수지, C5계 석유수지,C9계 석유수지, DCPD수지, 수첨 DCPD수지, 마레인화스티렌수지 등을 들 수 있다. 이들은 단독 또는 혼합하여 사용될 수 있다. 이들은 원하는 성능에 따라 적절히 선택된다. 이들은 단계(1) (A)의 폐폴리에스텔과 중량비율이 1:9 ∼ 9:1 비율로 혼합되는 것이 바람직하다.The PET which can be used in step (1) (A) is a polymer synthesized from terephthalic acid and ethylene glycol, and is a waste PET chip which is mechanically pulverized from waste PET bottle molded products produced during the production of PET fibers. , Terpene resins, petroleum resins and derivatives thereof, dicyclopentadiene and derivatives thereof, gum rosin, wood rosin, thalrosene, hydrogenated rosin, marinized rosin, rosin ester, pinene resin, dipentene resin, C5 Petroleum resins, C9 petroleum resins, DCPD resins, hydrogenated DCPD resins, marinized styrene resins, and the like. These may be used alone or in combination. These are appropriately selected depending on the desired performance. These are preferably mixed with the waste polyester of step (1) (A) in a ratio of 1: 9 to 9: 1.

단계(1) (B)에서 사용될 수 있는 다염기산은 무수프탈산, 이소프탈산, 테레프탈산, 아디핀산, 아제라인산, 세바신산, 무수테트라하이드로프탈산, 무수마레인산, 후말산, 이타곤산, 무수트리메리트산, 무수피로메리트산, 벤조산 등을 들 수 있다. 이들은 단독 또는 혼합하여 사용될 수 있다. 이들은 단계(1) (A)의 생성물에 10∼50중량%의 양으로 첨가되는 것이 바람직하다.The polybasic acids which may be used in step (1) (B) are phthalic anhydride, isophthalic acid, terephthalic acid, adipic acid, azeline acid, sebacic acid, tetrahydrophthalic anhydride, maleic anhydride, fumaric acid, itanoic acid, trimellitic anhydride, Pyromeric acid, benzoic acid, etc. are mentioned. These may be used alone or in combination. They are preferably added to the product of step (1) (A) in an amount of 10 to 50% by weight.

단계(2)에서 사용될 수 있는 다가알콜은 에틸렌글리콜, 프로필렌 글리콜, 1.3프로판디올, 1.3부탄디올, 1.6헥산디올, 네오펜틸글리콜, 디에틸렌글리콜, 디프로필렌글리콜, 폴리에필렌글리콜, 비스페놀A의 알킬렌옥사이드 부가물, 트리메틸올프로판,글리세린,펜타에리쓰리톨등이며 이들은 단독또는 혼합하여 사용될 수 있다. 이들은 단계(1)의 생성물에 10∼35중량%의 양으로 첨가하는 것이 바람직하다. 유기산금속 또는 주석계 촉매를 사용한다. 사용량은 반응물에 대하여 0.05∼0.5중량%이다.The polyhydric alcohols that may be used in step (2) are ethylene glycol, propylene glycol, 1.3 propanediol, 1.3 butanediol, 1.6 hexanediol, neopentyl glycol, diethylene glycol, dipropylene glycol, polypropylene glycol, alkylene of bisphenol A Oxide adducts, trimethylolpropane, glycerin, pentaerythritol and the like, which may be used alone or in combination. They are preferably added in an amount of 10 to 35% by weight to the product of step (1). Organic acid metal or tin catalysts are used. The amount used is 0.05 to 0.5% by weight based on the reactants.

단계(3)에서 사용될 수 있는 염기성 화합물은 수산화나트륨, 수산화칼륨, 수산화암모늄, 수산화리튬, 아민류등이고 이들은 단독 또는 혼합하여 사용될 수 있다. 이들은 단계(2)에서 얻어진 생성물에 중화 및 수용화용으로 사용하며 5∼30중량%의 양을 첨가하는 것이 바람직하다. 단계(3)에서 사용될 수 있는 용제는 알콜류, 에텔류, 아세톤, 디메틸토를아미드, 테트라하이드로푸관, 에탈글리콜,프로필글리콜, 부틸글리콜 등이며 이들은 단독 또는 혼합하여 사용될 수 있다. 10∼50중량%양으로 첨가하는 것이 바람직하다.The basic compounds which can be used in step (3) are sodium hydroxide, potassium hydroxide, ammonium hydroxide, lithium hydroxide, amines and the like, which can be used alone or in combination. These are used for neutralization and solubilization to the product obtained in step (2), and it is preferable to add an amount of 5 to 30% by weight. Solvents that can be used in step (3) are alcohols, ethers, acetone, dimethyltoalamide, tetrahydrofu tube, etaglycol, propylglycol, butylglycol and the like, which can be used alone or in combination. It is preferable to add in the amount of 10-50 weight%.

본 발명의 제조방법은 반응기에 (1)전처리된 폐PET와 고체 해중합제를 10:1∼1:1 비율로 넣고 주석계 촉매 0.05∼0.5중량%첨가하여 180∼280℃온도에서 1차 해중합하고 150℃이하로 냉각하여 상기생성물에 (2)다염기산을 10∼50중량% 첨가하여 160∼260℃온도에서 해중합과 부가반응을 시켜서 산가 10∼150mgKOH/g 반응생성물을 제조하고 여기에 다가알콜을 10∼50중량% 첨가한후 200∼260℃ 온도에서 축중합하여 산가 10∼90mgKOH/g, 연화점 70∼150℃, 중량평균분자량 3,000∼50,000 폴리에스테르수지를 제조하고 이 수지에 염기성화합물을 첨가하여 물 또는 친수성 용제 및 이 용제에 물을 혼합한 용액에 용해하여 폴리에스틸 수용성 수지조성물을 제조하여 산가 10mgKOH/g이하 수지를 그대로 고형수지로 제품화하는 것을 포함하는 수용성 폴리에스텔 수지조성물을 제조하는 것을 특징으로 한다. 이 수용성 폴리에스텔 수지조성물은 폐 PET를 재활용하여 생성되지만 상기 원재료들의 조성비율에 따라 원하는 연화점, 상용성, 접착성이 양호하고 고기능의 물성을 얻을 수 있을 뿐만 아니라 저비용으로 고부가 가치가있는 첨단 신소재를 탄생시킬 수 있다는 것이 특징인데 특히 이 수용성 폴리에스텔 수지 조성물은 복사기, 프린트기, 전자사진용장치에 사용되는 토너를 중합법으로 제조시에 결착제, 잉크젯잉크 결착제 등으로 사용하고 한편 산가 10mgKOH/g이하의 고형수지는 인쇄잉크, 도료, 접착제, 분쇄법토너의 결착제 수지로 사용가능한 폴리에스텔 수지조성물을 제조하는 것을 특징으로 한다.In the production method of the present invention, (1) pre-treated waste PET and solid depolymerization are added in a ratio of 10: 1 to 1: 1, and 0.05 to 0.5% by weight of tin catalyst is first depolymerized at 180 to 280 ° C. 10 to 50% by weight of (2) polybasic acid is added to the product by cooling to below 150 ° C. to depolymerization and addition reaction at a temperature of 160 to 260 ° C. to prepare an acid value of 10 to 150 mg KOH / g reaction product. After adding 50 wt%, condensation polymerization at a temperature of 200 to 260 ° C. to prepare an acid value of 10 to 90 mg KOH / g, a softening point of 70 to 150 ° C., and a weight average molecular weight of 3,000 to 50,000 polyester resin were added to the resin to add water or Preparing a water-soluble polyester resin composition comprising dissolving a hydrophilic solvent and a solution of water in the solvent to produce a polyester water-soluble resin composition, and producing an acid value of 10 mg KOH / g or less resin as a solid resin. It features. This water-soluble polyester resin composition is produced by recycling waste PET, but according to the composition ratio of the raw materials, it is possible to obtain high-performance new materials with high added value at low cost as well as obtaining a desired softening point, compatibility, adhesion, and high functional properties. In particular, this water-soluble polyester resin composition is used as a binder, an inkjet ink binder, etc. when producing toners used in photocopiers, printers, and electrophotographic apparatuses by a polymerization method, and has an acid value of 10 mgKOH / g. The following solid resins are characterized by producing a polyester resin composition which can be used as a binder resin for printing inks, paints, adhesives, grinding methods and toners.

본 발명의 폴리에스텔 수지조성물은 (1) 전자사진, 정전하기록등에 정전하 화상을 현상시키는데 사용되는 토너용 수지 결착제로 사용되어 여기에 착색제, 전하제, 이형제 등을 첨가하여 중합법 또는 분쇄법으로 토너를 제조한다. 착색제는 카본블랙, 마그네타이트 등 흑색안료, 산화철황, 한자옐로우, 퍼마넌트옐로우등 황색안료. 프탈로시아닌블루, 바이로렛트 등 청색안료. 산화철적, 카민, 톨루이진레트, 퀴나크리돈레등 적색안료. 프탈로시아닌그린, 크롬그린등 녹색안료등이 사용되고 착색제 함유량은 1∼40중량%이다. 전하제어제는 (+)대전 전하제어제는 니그로신계 염료, 4급암모늄염 등이있고 대표적상품명은 BONTRON N-07. BONTRON N-21 오리엔탈화학(주)이고 부(-)대전 전하조절제는 아조계금속착염, 살리실산계금속착염등이고 대표적 상품명은 BONTRON S-34, BONTRON E-84, 오리엔트화학(주)이고 전하제어제 사용량은 결착 수지에 대하여 0.5∼5중량%사용이 바람직하다.The polyester resin composition of the present invention (1) is used as a resin binder for toners used for developing electrostatic images in electrophotographic images, electrostatic notes, and the like, by adding a colorant, a charge agent, a mold release agent, or the like to a polymerization method or a grinding method. Toner is prepared. The colorants are black pigments such as carbon black and magnetite, yellow pigments such as iron oxide, sulfur kanji yellow, and permanent yellow. Blue pigments such as phthalocyanine blue and viloret. Red pigments such as iron oxide, carmine, toluzinet and quinacridone. Green pigments, such as phthalocyanine green and chrome green, are used, and a coloring agent content is 1-40 weight%. Charge control agents include (+) charge Charge control agents include nigrosine dyes and quaternary ammonium salts. Typical product names are BONTRON N-07. BONTRON N-21 Oriental Chemical Co., Ltd. and negative charge control agents are azo metal complex salts, salicylic acid metal complex salts, etc. Typical product names are BONTRON S-34, BONTRON E-84, Orient Chemical Co., Ltd. The amount of use is preferably 0.5 to 5% by weight based on the binder resin.

이형제는 폴리에틸렌 왁스, 폴리프로필렌 왁스, 고급지방산에스테르, 고급지방족알콜, 카나바왁스, 몬탄왁스등을 단독 또는 혼합하여 결착수지에 대하여 0.5∼10중량%등이 있다. 이들 첨가제는 결착수지에 잘 분산 되어야만 만족할만한 화상을 형성 시킬수가 있다.The release agent may be 0.5 to 10% by weight of the binder resin alone or in combination with polyethylene wax, polypropylene wax, higher fatty acid ester, higher aliphatic alcohol, canava wax, and montan wax. These additives must be well dispersed in the binder resin to form satisfactory images.

본 발명의 폴리에스텔수지 조성물은 물 또는 수친화성 용제 및 이용제와 물의 혼합용제에 잘 분산 용해되므로 액상수지조성물을 제조한후 여기에 상기 첨가제들을 분산시켜서 중합법으로 토너를 제조할 수 있고 또한 분쇄법으로 토너를 제조할 경우 본 발명의 폴리에스텔 수지 조성물의 고체 수지상태로 사용할 시에도 분자내에 계면활성제기능을 하는 관능기가 함유되어 있으므로 상기 첨가제를 잘분산시켜서 성능이 우수한 토너를 제조할수 있게 된다.Since the polyester resin composition of the present invention is well dispersed and dissolved in water or a water affinity solvent and a solvent and a mixed solvent of water, a toner may be prepared by polymerization by dispersing the additives therein after preparing a liquid resin composition. When manufacturing the toner by the method, even when used in the solid resin state of the polyester resin composition of the present invention, since the functional group contains a surfactant function in the molecule, it is possible to prepare the toner having excellent performance by dispersing the additive well.

이렇게 얻어진 토너는 레오미터에 의한 유출개시(Tfb)가 80∼95℃, 유출종료온도(Tend) 120∼135℃인 토너를 얻을 수 있으므로 화상형성 속도가 빠르고 저온 정착이 가능하고 오프섹 저항성이 양호하여 선명한 화상과 고품위의 화상을 얻을 수 있다.The toner thus obtained can obtain a toner having an outflow start (Tfb) of 80 to 95 DEG C and a discharge end temperature (Tend) of 120 to 135 DEG C by a rheometer, so that the image formation speed is fast, low temperature fixing is possible, and the off-section resistance is good. It is possible to obtain a clear image and a high quality image.

(2) 에폭시 수지를 경화제로 하는 분체도료 조성물을 제조시에 본발명의 폴리에스텔 조성물은 고분자 사슬말단에 카복실기를 2∼3개 갖고 있으므로 반응성이 좋고 분산성이 좋으므로 블록킹방지제를 소량첨가해도 저장 안정성도 있을 수 있으며 저연화점 수지이므로 180℃이하에서 10분정도의 짧은 시간에 경화 반응이 가능하여 여기서 경화온도를 낮출수 있어서 고광택, 내열성, 내악품성등이 우수한 고품질의 도막을 얻을 수 있다.(2) The polyester composition of the present invention has two to three carboxyl groups at the end of the polymer chain when preparing a powder coating composition using an epoxy resin as a curing agent, so that the reactivity is good and the dispersibility is good. There may also be stability, and the low softening point resin can be cured in a short time of about 10 minutes at 180 ℃ or less, whereby the curing temperature can be lowered to obtain a high-quality coating film excellent in high gloss, heat resistance, anti-corrosiveness, and the like.

(3) 유변성 알키드바니쉬 도료 및 인쇄잉크 제조시 있어서 본 발명 폴리에스텔 수지조성물을 고형수지 성분으로 하고 지방산 및 건성유를 기하여 반응 시켜서 얻은 생성물은 지방족탄화수소계 용제나 방향족 탄화수소계 용제에 용해성이 좋고 우수한 광택과 내수성, 내후성이 좋은 강견한 도막과 고품질의 인쇄화면을 얻을 수 있고, 그라비아잉크에서 본발명의 폴리에스텔 조성물은 케튼계용제와 방향족 탄화수소계 용제의 혼합용젱 용해성이 좋아서 속건성, 부착성, 내마모성, 견뢰성이 우수한 인쇄화면을 얻을 수 있다.(3) In the production of rheology alkyd varnish paints and printing inks, the product obtained by reacting the polyester resin composition of the present invention as a solid resin component with fatty acids and dry oils is well soluble in aliphatic hydrocarbon solvents and aromatic hydrocarbon solvents. A strong coating film with good gloss, water resistance, and weather resistance and a high quality printed screen can be obtained. The polyester composition of the present invention from gravure ink has a good solubility in mixing of ketone solvents and aromatic hydrocarbon solvents, so it is fast-drying, adhesion and abrasion resistance. A printed screen with excellent fastness can be obtained.

(4) 접착제 제조시에 본 발명의 폴리에스텔 수지 조성물을 접착제 기본 고착수지로 사용시에 핫멜트 접착제에 사용시에는 저연화점, 저용윰점도, 부착성, 내수성,내약품성, 가속성, 상용성들이 우수하며, 종이, 보드류, 가죽, 직물, 목재, 플라스틱, 금속, 알미늄등 금속 등에 우수한 초기 접착 및 강견한 접착력을 얻을 수 있고 이들 접착제는 각종 용제에 용해시켜 액상 접착제로 상기의 피접착기제에 동일한 용도로 사용할 수 있다.(4) When the polyester resin composition of the present invention is used as an adhesive base fixing resin in the manufacture of the adhesive, and the hot melt adhesive is used, it has excellent low softening point, low melt viscosity, adhesion, water resistance, chemical resistance, acceleration, and compatibility. Excellent initial adhesion and strong adhesion can be obtained for paper, boards, leather, textiles, wood, plastics, metals, aluminum and other metals. These adhesives can be dissolved in various solvents and used for the same purpose as the liquid adhesive as the liquid adhesive. Can be.

실시예에 의해 상세히 설명하지만 이 실시예에 의해 본 발명이 한정되지는 않는다.Although an Example demonstrates in detail, this invention is not limited by this Example.

<실시예 1><Example 1>

단계(1) 교반기, 환류냉각기, 분리기, 온도계, 질소주입구를 설치한 반응기에 폐PET를 분쇄한 칩 400g, 검조진 200g, 주석산촉매 모노부탄 0.3g을 사입하여 질소주입하에서 250℃로 가열하여 내용물을 2시간 유지한다. 온도가 상승하면서 PET가 점차로 용해되어 가면 교반을 시작한다. 내용물이 투명해지는 것을 확인한 후, 내용물은 150℃로 냉각하여 무수마레인산 12Og을 가하여 내용물의 온도가 고리개방 반응의 발생열이 완료되는 시점을 확인후 재 가열하여 235℃에서 3시간 반응시킨다. 해 중합 생성물의 산가는 115mgKOH/g이다. 단계(2) 여기에 비르페놀A에틸렌옥사이드부가물 200g을 가하여 250℃에서 5시간 동안 탈수하면서 축중합을 한후 산가 55mgKOH/g에 도달하면 반응생성물을 냉각하여 수산화나트륨 50g, 과중류수 1500g을 가하여 85℃에서 30분간 교반한 후 종료하여 수용성 폴리에스텔수지(수지용액 A로 지칭한)를 제조하였다. 상기 생성물은 산가 39mgKOH/g, 중량평균 분자량 11,000 연화점 80℃, PH 8.5이다.Step (1) Into a reactor equipped with a stirrer, a reflux condenser, a separator, a thermometer, and a nitrogen inlet, 400 g of waste PET chips, 200 g of gumzojin, and 0.3 g of tartaric acid catalyst monobutane were heated and heated to 250 ° C. under nitrogen injection. Hold for 2 hours. As the temperature rises, the PET gradually dissolves and begins to stir. After confirming that the contents became transparent, the contents were cooled to 150 ° C. and 12Og of maleic anhydride was added to confirm the timing at which the temperature of the contents completed the heat of the ring-opening reaction. The acid value of the polymerization product is 115 mgKOH / g. Step (2) 200 g of birphenol Aethylene oxide adduct was added thereto, followed by condensation polymerization while dehydration at 250 ° C. for 5 hours. When the acid value reached 55 mgKOH / g, the reaction product was cooled and 50 g of sodium hydroxide and 1500 g of supernatant water were added thereto. After stirring at 30 DEG C for 30 minutes, a water-soluble polyester resin (referred to as resin solution A) was prepared. The product had an acid value of 39 mgKOH / g, a weight average molecular weight of 11,000 softening point of 80 ° C., and PH of 8.5.

상기 수용성 폴리에스텔 수지를 중합토너 결착제로 사용하여 중합법으로 토너를 제조하였다 물성이 좋고 정착성이 우수한 토너를 제조할 수 있었다.Toner was prepared by a polymerization method using the water-soluble polyester resin as a polymerized toner binder. A toner having good physical properties and excellent fixability could be prepared.

수지용액A 100중량부, 카본블랙 3중량부 전하제 0.1중량부 이형제 1중량부를 혼합분산시키고 현탁시켜 입자를 만들고 여과하여 얻은 입자를 수세하고 건조하여 토너침전물을 만든후 토너조성물 100중량부에 외첨제1중량부를 첨가하여 토너를 만들어 프린터 카트리지에 충진하고 프린트를 시행하였다. 화상을 형성시킨 결과 선명한 화상과 정착성이 우수한 화상을 얻을 수가 있었다.100 parts by weight of resin solution A, 3 parts by weight of carbon black, 0.1 parts by weight of charge agent, 1 part by weight of dispersant is mixed, dispersed and suspended to form particles, and the particles obtained by filtration are washed with water and dried to form a toner precipitate. Toner was added by adding 1 part by weight of the toner to fill the printer cartridge, and the printing was performed. As a result of forming the image, a clear image and an image excellent in fixability were obtained.

<실시예 2><Example 2>

폐PET칩 400g, 수첨로진 200g, 주석산모노부틴 0.3g, 무수트리메리트산 150g, 네오펜틸글리콘 200g을 반응기에 삽입하고 실시예(1)과 동일한 방법으로 실시하였다. (수지용액 B로 지칭한다. )400 g of waste PET chip, 200 g of hydrogenated rosin, 0.3 g of monobutane stannate, 150 g of trimellitic anhydride, and 200 g of neopentylglycone were inserted into a reactor and carried out in the same manner as in Example (1). (Referred to as resin solution B.)

상기 수용성 폴리에스텔의 수지 산가는 30mgKOH/g이고 중량평균 분자량은 12,000 연화점 95℃, PH 8.7이다.The resin acid value of the said water-soluble polyester is 30 mgKOH / g, and a weight average molecular weight is 12,000 softening point of 95 degreeC, and PH 8.7.

상기 수용성 폴리에스텔 수지를 중합토너 결착제로 사용하여 중합법으로 토너를 제조하였다 물성이 좋고 정착성이 우수한 토너를 제조할 수 있었다.Toner was prepared by a polymerization method using the water-soluble polyester resin as a polymerized toner binder. A toner having good physical properties and excellent fixability could be prepared.

수지용액B 100중량부, 카본블랙 3중량부 전하제 0.1중량부 이형제 1중량부를 혼합분산시키고 현탁시켜 입자를 만들고 여과하여 얻은 입자를 수세하고 건조하여 토너침전물을 만든후 토너조성물 100중량부에 외첨제1중량부를 첨가하여 토너를 만들어 프린터 카트리지에 충진하고 프린트를 시행하였다. 화상을 형성시킨 결과 선명한 화상과 정착성이 우수한 화상을 얻을 수가 있었다.100 parts by weight of resin solution B, 3 parts by weight of carbon black, 0.1 parts by weight of charge agent, 1 part by weight of dispersant was mixed, dispersed and suspended to form particles, and the particles obtained by filtration were washed with water, dried to form a toner precipitate, and then to 100 parts by weight of toner composition. Toner was added by adding 1 part by weight of the toner to fill the printer cartridge, and the printing was performed. As a result of forming the image, a clear image and an image excellent in fixability were obtained.

<실시예 3><Example 3>

반응기에 폐PET칩 400g, 로진에스텔 200g, 주석산 모노부틸 0.3g, 푸말산 150g 네오펜틸글라콜 100g, 디에틸렌글리콜 100g을 반응기에 사입하고 실시예 1)과 동일한 방법으로 실시하고 중화제로 수산화칼륨 55g으로 대체하였다. 상기 수용성폴리에스텔수지 산가는 28mgKOH/g이고 중량평균분자량은 12,000, 연화점은 105℃, PH 8.1이다.400 g of waste PET chips, 200 g of rosin esters, 0.3 g of monobutyl stannate, 150 g of fumaric acid, 100 g of neopentyl glycol, and 100 g of diethylene glycol were charged into the reactor, and the same procedure as in Example 1) was carried out. Replaced by. The acid value of the water-soluble polyester resin is 28 mgKOH / g, the weight average molecular weight is 12,000, the softening point is 105 ℃, PH 8.1.

<실시예 4><Example 4>

폐PET칩 400g, C5석유수지 200g, 주석산 모노부틸 0.3g,무스트리메리트산 150g 에틸렌글리콜 100g, 트리메틸롤프로판 80g 반응기에 사입하고 실시예 1)과 동일한 방법으로 실시하고 중화제로 수산화암모늄 50g 대체하고 수친화성용제로 부틸글리콘 200g을 사용하였다. 상기 수용성 폴리에스텔 수지 산가는 30mgKOH/g이고 중량평균 분자량은 13,000, 연화점은 108℃, PH 7.9이다400g of waste PET chip, 200g of C5 petroleum resin, 0.3g of monobutyl stannate, 150g of ethylene glycol, 100g of ethylene glycol, trimethylolpropane, 80g, was introduced into a reactor, and was carried out in the same manner as in Example 1) and replaced with 50g of ammonium hydroxide as a neutralizing agent. 200 g of butylglycone was used as the water affinity solvent. The acid value of the water-soluble polyester resin is 30 mgKOH / g, the weight average molecular weight is 13,000, the softening point is 108 ℃, PH 7.9.

<실시예 5>Example 5

폐PET칩 400g, C9석유수지 200g, 주석산 모노부틸 0.3g, 아디핀산 50g, 무수바레인산 100g, 프로필렌글리콜 100g, 네오펜틴글리콘 100g을 반응기에 사입하고 실시예 1)과 동일한 방법으로 실시하고 중화제로 수산화나트륨 30g, 트리에틸아민 35g을 사용하였다.상기 수용성 폴리에스텔수지 산가는 31mgKOH/g이고 중량평균 분자량은 13,000, PH 7.7이다400 g of waste PET chips, 200 g of C9 petroleum resin, 0.3 g of monobutyl tartarate, 50 g of adipic acid, 100 g of baric anhydride, 100 g of propylene glycol, and 100 g of neopentin-glycone were introduced into the reactor, followed by the same method as in Example 1). 30 g of sodium hydroxide and 35 g of triethylamine were used. The acid value of the water-soluble polyester resin was 31 mgKOH / g, and the weight average molecular weight was 13,000, PH 7.7.

<실시예 6><Example 6>

폐PET칩 350g, 마레인화검로진 250g, 주석산 모노부틸 0.3g, 무수트리메리트산 100g, 네오펜틴글리콜 50g, 비스페놀A에틸렌복사이드 부가물 150g을 반응기에 사입하고 실시예 1과 동일한 방법으로 실시하였다.350 g of waste PET chip, 250 g of marinated gumzine, 0.3 g of monobutyl stannate, 100 g of trimellitic anhydride, 50 g of neopentin glycol, and 150 g of bisphenol Aethylene double side adduct were introduced into a reactor and carried out in the same manner as in Example 1. It was.

상기 수용성 폴리에스텔 수지 산가는 45mgKOH/g이고 중량평균 분자량은 11,500, 연화점은 81℃, PH 8.7이다The acid value of the water-soluble polyester resin is 45mgKOH / g, the weight average molecular weight is 11,500, the softening point is 81 ℃, PH 8.7.

<실시예 7><Example 7>

폐PET칩 350g, 디싸이크로펜타디엔레진 250g, 주석산 모노부틸 0.3g, 무수마레인산 150g, 네오펜틴글리콜 100g, 폴리에틸렌글리콜 100g을 반응기에 사입하고 실시예 1과 동일한 방법으로 실시하고 중화제로 수산화 암모늄 30g, 트리에틸아민 50g을 대체하였다. 상기 수용성 폴리에스텔수지 산가는 30mgKOH/g이고 중량평균 분자량은 12,000, 연화점은 95℃, PH 8.1이다350 g of waste PET chips, 250 g of dicyclopentadiene resin, 0.3 g of monobutyl stannate, 150 g of maleic anhydride, 100 g of neopentin glycol, and 100 g of polyethylene glycol were introduced into a reactor, and the same procedure as in Example 1 was carried out. 30 g, 50 g triethylamine was replaced. The acid value of the water-soluble polyester resin is 30mgKOH / g, the weight average molecular weight is 12,000, the softening point is 95 ℃, PH 8.1

<실시예 8><Example 8>

폐PET칩 400g, 디싸이크로펜타디엔레진 200g, 주석산 모노부틸 0.3g, 이소프탈산 100g, 아디핀산 50g, 네오펜틸글리콜 70g, 비스페놀A에틸렌 옥사이드부가물 120g을 반응기에 사입하고 실시예 1과 동일한 방법으로 실시하였으나 단계(3)의 중화와 수용화 단계는 생략하고 고형폴리에스텔 수지를 제조하였다. 상기 고형폴리에스텔수지 산가는 10mgKOH/g이고 중량평균 분자량은 20,000, 연화점은 93℃이다400 g of waste PET chip, 200 g of dicyclopentadiene resin, 0.3 g of monobutyl stannate, 100 g of isophthalic acid, 50 g of adipic acid, 70 g of neopentyl glycol, and 120 g of bisphenol Aethylene oxide adduct were added to the reactor and the same method as in Example 1 Although the neutralization and solubilization step of step (3) was omitted, a solid polyester resin was prepared. The acid value of the solid polyester resin is 10mgKOH / g, the weight average molecular weight is 20,000, the softening point is 93 ℃.

<실시예 9>Example 9

폐PET칩 500g, 검로진 200g, 주석산 모노부틸 0.3g, 무수마레인산 100g, 펜타에리쓰리톨 200g을 반응기에 사입하고 실시예 1과 동일한 방법으로 실시하였으나 단계(3)의 중화와 수용화 단계는 생략하고 고형폴리에스텔수지를 제조하였다. 상기고형폴리에스텔수지는 산가 11mgKOH/g이고 중량평균 분자량은 30,000, 연화점은 145℃이다500 g of waste PET chip, 200 g of gum rosin, 0.3 g of monobutyl stannate, 100 g of maleic anhydride, and 200 g of pentaerythritol were introduced into the reactor and carried out in the same manner as in Example 1, but the neutralization and solubilization steps of step (3) were performed. Omitted to prepare a solid polyester resin. The solid polyester resin has an acid value of 11 mgKOH / g, a weight average molecular weight of 30,000, and a softening point of 145 ° C.

본 발명에 의한 폐PET로 제조된 폴리에스텔 수지는 착색제, 기타첨가제와 상용성과 분산성이 우수하고 매체와의 부착성이 우수할 뿐만 아니라 중화 및 수용화가 가능하여 첨단신소재로 응용되어 중합법으로 제조되는 복사기, 프린터, 전자 사진용 화상현상용 토너의 결착제로 사용할 수 있고 고형수지는 분쇄법 토너의 결착제로 사용할 수 있고 인쇄잉크, 도료, 접착제의 고착수지로 제공된다. 본 발명은 자원재생의 관점에서 환경친화성과 사회적 가치를 지니는 고부가 가치 소재로 안정적으로 제조할 수 있다.The polyester resin produced from the waste PET according to the present invention is excellent in compatibility and dispersibility with colorants and other additives, has excellent adhesion to the medium, and is capable of neutralization and solubilization. It can be used as a binder of copiers, printers, electrophotographic imaging toners, and a solid resin can be used as a binder of a pulverized toner, and is provided as a fixing resin of printing ink, paint and adhesive. The present invention can be stably manufactured from high value-added materials having environmental friendliness and social value in terms of resource recycling.

Claims (16)

(1) (A) 폴리에틸렌테레프탈레이트를 고체수지용해제로 1차 해중합하고, (B)상기 용해물에 다염기산을 가하여 2차 해중합 및 부가반응을 시키는 단계(1) a first depolymerization of (A) polyethylene terephthalate with a solid resin solution, and (B) a second depolymerization and an addition reaction by adding a polybasic acid to the lysate. (2) 단계(1)에서 얻어진 생성물에 다가알콜을 가하여 축중합 반응을 시켜 산가 10∼150mgKOH/g의 중량 평균분자량 3,000∼50,000, 연화점 70∼150℃의 중합체를 제조하는 단계(2) adding polyhydric alcohol to the product obtained in step (1) to perform a polycondensation reaction to prepare a polymer having a weight average molecular weight of 3,000 to 50,000 and a softening point of 70 to 150 ° C. with an acid value of 10 to 150 mgKOH / g. (3) 단계(2)에서 얻어진 중합체중 산가 20mgKOH/g 이상의 중합체는 고형수지 원상태로 제조하거나 염기성화합물로 중화 및 수용화하기 위하여 물 또는 수친화성 용제 및 이용제의 물 혼합물에 용해 및 희석시켜 수용성 폴리에스텔수지를 제조하고 산가 15mgKOH/g이하의 중합체는 그대로 고형수지로 제조하므로써 상기 중합체의 일정하중 압출세관식레오미터에 의한 유출개시온도(Tfb)가 80℃∼105℃, 유출 종료온도(Tend)가 120℃∼160℃, 유리전이제(Tg)이 40℃∼80℃인 것을 특징으로 하는 폐폴리에틸렌테레프탈레이트를 재활용하여 고부가가치의 폴리에스텔 수지의 제조방법(3) A polymer having an acid value of 20 mg KOH / g or more in the polymer obtained in step (2) is dissolved in water or a water-soluble solvent and a mixture of water-soluble solvents and water-soluble to prepare a solid resin or neutralize and solubilize it with a basic compound. Since the polyester resin is prepared and the polymer having an acid value of 15 mgKOH / g or less is produced as a solid resin, the outflow start temperature (Tfb) of the polymer by a constant load extruded tubular rheometer is 80 ° C to 105 ° C, and the outflow end temperature (Tend ) Is a method for producing a high value-added polyester resin by recycling waste polyethylene terephthalate, characterized in that 120 ℃ ~ 160 ℃, glass transition agent (Tg) is 40 ℃ ~ 80 ℃. 제 1항에 있어서 단계(1)(A)의 고체수지는 검로진, 우드로진, 탈로진, 수첨로진, 마레인화로진, 로진에스텔, 피넨수지, 디펜텐 수지, C5계 석유수지, C9계 석유수지, DCPD수지, 수첨 DCPD수지, 마레인화스티렌수지군중에서 선택되는 것을 특징으로하는 폴리에스텔 수지조성물의 제조방법The solid resin of step (1) (A) is gum rosin, wood rosin, deloginate, hydrogenated rosin, marinized rosin, rosin ester, pinene resin, dipentene resin, C5 petroleum resin, C9 series petroleum resin, DCPD resin, hydrogenated DCPD resin, a method of producing a polyester resin composition characterized in that selected from the group 제 1항에 있어서 단계(1)(A)의 폴리에틸렌테레프탈레이트와 고체수지용해제의 중량비율이 1:9∼9:1인 것을 특징으로 하는 폴리에스텔 중합체의 제조방법The method for producing a polyester polymer according to claim 1, wherein the weight ratio of the polyethylene terephthalate and the solid resin solution in step (1) (A) is 1: 9 to 9: 1. 제 1항에 있어서 단계(1)(B)의 해중합을 동반하는 부가반응용 다염기산은 무수프탈산, 이소프탈산, 테레프탈산, 아디핀산, 아제라인산, 세바신산, 무수테트라하이드로프탈산, 무수마레인산, 후말산, 이타곤산, 무수트리메리트산, 무수피로메리트산, 벤조산군 중에서 선택되는 것을 특징으로 하는 폴리에스텔 수지조성물을 제조하는 방법The polybasic acid for addition reaction with depolymerization of step (1) (B) is phthalic anhydride, isophthalic acid, terephthalic acid, adipic acid, azeline acid, sebacic acid, tetrahydrophthalic anhydride, maleic anhydride, fumaric acid. , Itaconic acid, trimellitic anhydride, pyromellitic anhydride, a method for producing a polyester resin composition, characterized in that selected from the group of benzoic acid 제 1항에 있어서 단계(1)(B)의 다염기산은 (A)의 생성물에 대하여 10∼70중량%의 양으로 첨가되는 것을 특징으로하는 중합체의 제조방법The process for producing a polymer according to claim 1, wherein the polybasic acid of step (1) (B) is added in an amount of 10 to 70% by weight relative to the product of (A). 제 1항에 있어서 단계(1)의 해중합 및 부가반응과 중축합용 촉매를 0.05∼0.5중량%의 량으로 사용하여 반응 온도를 200∼250℃에서 실행하는 것을 특징으로 하는 제조방법The method according to claim 1, wherein the reaction temperature is carried out at 200 to 250 DEG C using the catalyst for depolymerization and addition reaction and the polycondensation in step (1) in an amount of 0.05 to 0.5% by weight. 제 1항에 있어서 단계(2)의 다가알콜은 에틸렌글리콜, 프로필펜 글리콜, 1.3프로판디올, 1.3부탄디올, 1.6헥산디올, 네오펜틸글리콜, 디에틸렌글리콜, 디프로필렌글리콜, 폴리에필렌글리콜, 비스페놀A의 알킬렌옥사이드 부가물, 트리메틸올프로판,글리세린,펜타에리쓰리톨군중에서 선택되는 것이 특징인 폴리에스텔 수지조성물의 제조방법The polyhydric alcohol of step (2) is ethylene glycol, propylphen glycol, 1.3 propanediol, 1.3 butanediol, 1.6 hexanediol, neopentyl glycol, diethylene glycol, dipropylene glycol, poly ethylene glycol, bisphenol A Method for producing a polyester resin composition, characterized in that selected from the group of alkylene oxide adducts, trimethylolpropane, glycerin, pentaerythritol 제 1항에 있어서 단계(2)의 다가알콜은 단계(1)의 해중합물에 대하여 10∼70중량%의 양으로 첨사하여 산가 10∼90mgKOH/g 인 것을 특징으로하는 폴리에스텔의 제조방법The method of producing a polyester according to claim 1, wherein the polyhydric alcohol of step (2) is added in an amount of 10 to 70% by weight based on the depolymerized product of step (1) and has an acid value of 10 to 90 mgKOH / g. 제 1항에 있어서 단계(3)의 중화용 염기성 화합물은 수산화나트륨, 수산화칼륨, 수산화암모늄, 수산화리튬, 아민류군 중에서 선택하는 것이 특징인 폴리에스텔 조성물의 제조방법The method for preparing a polyester composition according to claim 1, wherein the basic compound for neutralization in step (3) is selected from the group consisting of sodium hydroxide, potassium hydroxide, ammonium hydroxide, lithium hydroxide, and amines. 제 1항에 있어서 단계(3)의 중화용 염기성 화합물은 단계(2)의 산가 20mgKOH/g∼l50mgKOH/g의 생성물에 대하여 3∼30중량%의 양으로 첨가하여 수용성 폴리에스텔 수지조성물이 가능하도록 하는 것을 특징으로 하는 폴리에스텔수지 제조방법The neutralizing basic compound according to claim 1 is added in an amount of 3 to 30% by weight based on the acid value of 20 mgKOH / g to l50 mgKOH / g in step (2) to enable a water-soluble polyester resin composition. Polyester resin manufacturing method characterized in that 제 1항에 있어서 염기성 화합물로 중화된 생성물에 사용하는 수친화성 용제는 알콜류, 에텔류, 아세톤, 디아세톤알콜, 디메틸토를아미드, 테트라하이드로푸관, 에틸글리콜, 프로필글리콜, 부틸글리콜, n-메틸피롤리돈군 중에서 선택하는 것을 특징으로 플리에스텔수지 조성물의 제조방법The water affinity solvent used for the product neutralized with a basic compound is alcohol, ether, acetone, diacetone alcohol, dimethyl tolamide, tetrahydro-fu tube, ethyl glycol, propyl glycol, butyl glycol, n-methyl Method for producing a polyester resin composition, characterized in that selected from the group of pyrrolidone 제 1항에 있어서 염기성 화합물로 중화된 생성물에 물 또는 수친화성 용제및 이 용제의 물 혼합물을 1∼10배를 첨가하여 희석하는 것을 특징으로 하는 수분산성폴리에스텔의 제조방법The method for producing a water-dispersible polyester according to claim 1, wherein water or a water affinity solvent and a water mixture of the solvent are diluted by adding 1 to 10 times to a product neutralized with a basic compound. 제 1항에 있어서 단계(2)의 산가 10mgKOH/g∼150mgKOH/g의 생성물은 고형수지로 연화점이 70∼150℃, 유출개시온도(Tfb)가 80∼105℃, 유출종료온도(Tend)가 120℃ ∼160℃,유리전이점(Tg) 40∼80℃인 폴리에스텔 수지의 제조방법According to claim 1, the acid value of 10mgKOH / g ~ 150mgKOH / g of step (2) is a solid resin with a softening point of 70 ~ 150 ℃, the outflow start temperature (Tfb) is 80 ~ 105 ℃, the exit end temperature (Tend) is Process for producing a polyester resin having a temperature of 120 ° C. to 160 ° C. and a glass transition point (Tg) of 40 ° C. to 80 ° C. 제 10항에 있어서 수용성 폴리에스텔 수지 조성물은 잉크젯 및 중합법토너의 결착 수지용으로 적합한 폴리에스텔 수지조성물의 제조방법The method for producing a polyester resin composition according to claim 10, wherein the water-soluble polyester resin composition is suitable for binder resins of inkjet and polymerization process toners. 제 13항에 있어서 저연화점 낮은 용융점도를 갖는 것을 특징으로 하는 고형수지는 분쇄법으로 제조하는 전자사진용 토너용 수지조성물The resin composition for an electrophotographic toner according to claim 13, wherein the solid resin has a low softening point and a low melt viscosity. 제 13항에 있어서 고형수지는 상용성, 부착성이 우수하여 인쇄잉크, 도료, 접착제용 수지조성물The resin composition according to claim 13, wherein the solid resin has excellent compatibility and adhesion, and thus, a resin composition for printing ink, paint, and adhesive.
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