JP2010516833A - PETG-type decorative panel for molding having moldability similar to PVC - Google Patents

PETG-type decorative panel for molding having moldability similar to PVC Download PDF

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JP2010516833A
JP2010516833A JP2009546314A JP2009546314A JP2010516833A JP 2010516833 A JP2010516833 A JP 2010516833A JP 2009546314 A JP2009546314 A JP 2009546314A JP 2009546314 A JP2009546314 A JP 2009546314A JP 2010516833 A JP2010516833 A JP 2010516833A
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ヨン−スン・アン
ミン−ホ・イ
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Abstract

本発明はPVCと類似した成形性を有するPETG系化粧板を提供する。ポリエチレンテレフタレートグリコール(PETG)樹脂にエステル系樹脂またはエラストマー樹脂を溶融混合したPETGアロイ樹脂を含む。これにより、PETG化粧板の表面品質は維持しつつ成形温度の範囲を広げることができ、また成形可能温度を既存対比3ないし10℃ほど下げることができる。  The present invention provides a PETG decorative board having formability similar to PVC. A PETG alloy resin in which an ester resin or an elastomer resin is melt-mixed with polyethylene terephthalate glycol (PETG) resin is included. Thereby, the range of the molding temperature can be expanded while maintaining the surface quality of the PETG decorative board, and the moldable temperature can be lowered by 3 to 10 ° C. as compared with the existing one.

Description

本発明は化粧板(decorative sheet)に関し、さらに詳しくはポリ塩化ビニル(PVC)と類似した成形性を有するポリエチレンテレフタレートグリコール(PETG)系化粧板に関する。   The present invention relates to a decorative sheet, and more particularly to a polyethylene terephthalate glycol (PETG) decorative board having formability similar to polyvinyl chloride (PVC).

PETG成形用化粧板の表面品質は優れているが、PVCと比較すると狭い成形温度範囲及び高い成形温度を有する。   Although the surface quality of the decorative sheet for PETG molding is excellent, it has a narrow molding temperature range and a high molding temperature as compared with PVC.

すなわち、PETG化粧板は優れた表面品質と成形性を有しているものの、狭い成形温度範囲によって2次的連続処理(例えば、成形)を実施するのに難点がある。成形温度が低い場合、成形品のコーナー部のほつれ、付着力の低下などが起こり、高い成形温度ではコーナー部の伸びまたは垂れが起こり、成形品質に比例して表面品質が低下する問題がある。   That is, although the PETG decorative board has excellent surface quality and moldability, there is a difficulty in performing secondary continuous processing (for example, molding) in a narrow molding temperature range. When the molding temperature is low, the corner portion of the molded product frays and the adhesive force is reduced. At a high molding temperature, the corner portion is stretched or drooped, and the surface quality is lowered in proportion to the molding quality.

日本特開2003-246916号には異なるガラス転移温度を有する3種のポリエステル樹脂を特定比率で配合して、特定の溶融体積流速(melt volume‐flow rate)を有する柔軟性ポリエステル化粧シート用組成物が開示されており、日本特開2005-298715号には前記柔軟性ポリエステル素材に無機物充填剤を用いて難燃性を与えた組成物が開示されている。しかし、PETG樹脂の成形可能温度を下げながらその成形可能な温度範囲を広げることに関する本発明とは相違している。   Japanese Patent Application Laid-Open No. 2003-246916 contains a composition for three types of polyester resins having different glass transition temperatures in a specific ratio, and a composition for a flexible polyester decorative sheet having a specific melt volume-flow rate. Japanese Unexamined Patent Publication No. 2005-298715 discloses a composition in which flame resistance is imparted to the flexible polyester material using an inorganic filler. However, the present invention is different from the present invention relating to expanding the temperature range where PETG resin can be molded while lowering the moldable temperature range.

日本特開2003-246916号Japanese Unexamined Patent Publication No. 2003-246916 日本特開2005-298715号Japanese Unexamined Patent Publication No. 2005-298715

本発明は前述した問題点を解決するために案出されたもので、その目的は成形物性をPVCと匹敵する低い成形温度と広い成形温度範囲で成形可能にしたPETG成形用化粧板を提供するところにある。   The present invention has been devised to solve the above-mentioned problems, and an object thereof is to provide a decorative sheet for PETG molding, which can be molded at a molding temperature as low as PVC and a wide molding temperature range comparable to PVC. By the way.

前述した目的を達成するために、本発明はポリエチレンテレフタレートグリコール(PETG)樹脂にエステル系樹脂またはエラストマー(elastomer)樹脂を溶融混合(alloy)したPETGアロイ樹脂を含む化粧板を提供する。   In order to achieve the above-mentioned object, the present invention provides a decorative board comprising a PETG alloy resin obtained by melt-mixing an ester resin or an elastomer resin with a polyethylene terephthalate glycol (PETG) resin.

本発明に係るPETGアロイ樹脂のガラス転移温度(Tg)は75±3℃であって、一般のPETG樹脂より3ないし7℃ほど低いことから、PVCと類似に低い温度で成形可能である。   The glass transition temperature (Tg) of the PETG alloy resin according to the present invention is 75 ± 3 ° C., which is about 3 to 7 ° C. lower than that of a general PETG resin, so that it can be molded at a low temperature similar to PVC.

また、本発明に係るPETGアロイ樹脂の成形可能な温度範囲は60ないし80℃であって、PVCと類似して広い温度範囲で成形可能である。一般のPETG樹脂の場合、成形可能な温度範囲は70℃ないし85℃である。   Further, the temperature range in which the PETG alloy resin according to the present invention can be molded is 60 to 80 ° C., and can be molded in a wide temperature range similar to PVC. In the case of general PETG resin, the moldable temperature range is 70 ° C to 85 ° C.

本発明においてアロイ成分として使用されるエステル系樹脂はポリブチレンテレフタレート(PBT: polybutylene terephthalate)であって、液状重合または固相重合で得られた樹脂が望ましく、エラストマー樹脂としては、PBT樹脂にポリエーテルグリコール(polyether glycol)を共重合したエラストマー樹脂が望ましい。   In the present invention, the ester resin used as the alloy component is polybutylene terephthalate (PBT), which is preferably a resin obtained by liquid polymerization or solid phase polymerization. An elastomer resin copolymerized with glycol is desirable.

本発明においてエステル系樹脂またはエラストマー樹脂の混合量はPETG100重量部に対して5ないし20重量部であることが望ましい。   In the present invention, the mixing amount of the ester resin or the elastomer resin is preferably 5 to 20 parts by weight with respect to 100 parts by weight of PETG.

アロイ成分の混合量が5phr未満の場合、Tg及び成形温度を下げる程度が微弱である。アロイ成分の混合量が20phrを越える場合、Tg及び成形温度が過度に下がり、樹脂を加工する際PBT及びエラストマー樹脂の特性によって化合物(compound)特性及びシート圧出性が低下するのでシート加工性が低下する。この時、PBT樹脂の耐化学的特性によってシートの表面加工性及び接着力が低下する。   When the mixing amount of the alloy component is less than 5 phr, the degree of lowering the Tg and the molding temperature is weak. When the amount of the alloy component exceeds 20 phr, the Tg and the molding temperature are excessively lowered, and the compound properties and the sheet extrudability are lowered depending on the properties of the PBT and the elastomer resin when the resin is processed. descend. At this time, the surface workability and adhesive strength of the sheet are reduced due to the chemical resistance of the PBT resin.

本発明はPETG樹脂に相溶性に優れるエステル系樹脂またはエラストマー樹脂をアロイすることによって、Tgを3ないし7℃程度低下させ、弾性率の減少率が徐々に低下することによって、PVCと類似した熱的挙動を有する化合物を製造することができる。したがって、この化合物で成形温度範囲が広くて低い温度で成形可能な化粧板の製造が可能である。   In the present invention, an ester resin or an elastomer resin having excellent compatibility with PETG resin is alloyed to reduce Tg by about 3 to 7 ° C., and the rate of decrease in elastic modulus is gradually decreased, so that heat similar to PVC is obtained. Can be produced. Therefore, it is possible to produce a decorative board that can be molded at a low temperature with this compound having a wide molding temperature range.

参考として、成形性をデータ化できる代表的な方法としては、DMA(dynamic mechanical analysis)を用いて弾性率の変化を測定する方法がある。   As a reference, a representative method that can convert the moldability into data includes a method of measuring a change in elastic modulus using DMA (dynamic mechanical analysis).

以上述べたように、本発明によればPETG樹脂にエステル系樹脂またはエラストマー樹脂をアロイすることによって、PETG化粧板の表面品質は維持しつつ成形温度の範囲を広げることができ、また成形可能温度を既存のPETG化粧板との対比で3ないし10℃ほど下げることができる。   As described above, according to the present invention, the range of the molding temperature can be expanded while maintaining the surface quality of the PETG decorative board by alloying the ester resin or the elastomer resin with the PETG resin. Can be lowered by about 3 to 10 ° C. in comparison with the existing PETG decorative board.

実施例1の化粧板に対するガラス転移温度と弾性率(storage modulus)変化を示したグラフである。It is the graph which showed the glass transition temperature with respect to the decorative board of Example 1, and a elasticity modulus (storage modulus) change. 実施例2の化粧板に対するガラス転移温度と弾性率変化を示したグラフである。It is the graph which showed the glass transition temperature with respect to the decorative board of Example 2, and elastic modulus change. 実施例3の化粧板に対するガラス転移温度と弾性率変化を示したグラフである。It is the graph which showed the glass transition temperature with respect to the decorative board of Example 3, and elastic modulus change. 実施例4の化粧板に対するガラス転移温度と弾性率変化を示したグラフである。It is the graph which showed the glass transition temperature with respect to the decorative board of Example 4, and elastic modulus change. 比較例の化粧板に対するガラス転移温度と弾性率変化を示したグラフである。It is the graph which showed the glass transition temperature and elastic modulus change with respect to the decorative board of a comparative example.

以下、本発明の実施の形態について詳細に説明する。   Hereinafter, embodiments of the present invention will be described in detail.

[実施例1]
PETG樹脂にPBT樹脂を10phr添加して圧出コンパウンディングした後、その混合物を0.5mmの厚さで圧出シーティング(extrusion-sheeting)した。
[Example 1]
After adding 10 phr of PBT resin to PETG resin and performing extrusion compounding, the mixture was subjected to extrusion-sheeting at a thickness of 0.5 mm.

[実施例2]
PETG樹脂にPBT樹脂を20phr添加して圧出コンパウンディングした後、その混合物を0.5mmの厚さで圧出シーティングした。
[Example 2]
After adding 20 phr of PBT resin to PETG resin and performing extrusion compounding, the mixture was subjected to extrusion sheeting to a thickness of 0.5 mm.

[実施例3]
PETG 樹脂にPBT共重合エラストマー樹脂を10phr添加して圧出コンパウンディングした後、その混合物を0.5mmの厚さで圧出シーティングした。
[Example 3]
After adding 10 phr of PBT copolymer elastomer resin to PETG resin and performing extrusion compounding, the mixture was subjected to extrusion sheeting to a thickness of 0.5 mm.

[実施例4]
PETG樹脂にPBT共重合エラストマー樹脂を20phr添加して圧出コンパウンディングした後、その混合物を0.5mmの厚さで圧出シーティングした。
[Example 4]
After adding 20 phr of PBT copolymer elastomer resin to PETG resin and performing extrusion compounding, the mixture was subjected to extrusion sheeting to a thickness of 0.5 mm.

[比較例]
PETG樹脂を0.5mmの厚さで圧出シーティングした。
[Comparative example]
PETG resin was extrusion-sheeted at a thickness of 0.5 mm.

図5から分かるように、既存PETG鏡面化粧板の場合、ガラス転移温度は74℃付近で低下し始めて84℃付近で最低点になる。   As can be seen from FIG. 5, in the case of the existing PETG mirror surface decorative plate, the glass transition temperature starts to decrease around 74 ° C. and reaches the lowest point around 84 ° C.

[試験例]
実施例1ないし4及び比較例の化粧板に対して、ガラス転移温度と弾性率変化をDMAを用いて測定した。
[Test example]
With respect to the decorative plates of Examples 1 to 4 and the comparative example, the glass transition temperature and the elastic modulus change were measured using DMA.

図1は実施例1(PETG+PBTアロイ樹脂、アロイ成分含量:10phr)に対する化粧板のガラス転移温度と弾性率変化を示したグラフであって、Tgは76℃であり、弾性率低下は65℃から始まった。   FIG. 1 is a graph showing a glass transition temperature and a change in elastic modulus of a decorative board with respect to Example 1 (PETG + PBT alloy resin, alloy component content: 10 phr). Tg is 76 ° C., and a decrease in elastic modulus is 65. Started from ℃.

図2は実施例2(PETG+PBTアロイ樹脂、アロイ成分含量:20phr)に対する化粧板のガラス転移温度と弾性率変化を示したグラフであって、Tgは74℃であり、弾性率低下は63℃から始まった。   FIG. 2 is a graph showing the glass transition temperature and the change in elastic modulus of the decorative board with respect to Example 2 (PETG + PBT alloy resin, alloy component content: 20 phr). Tg is 74 ° C., and the elastic modulus decrease is 63 Started from ℃.

図3は実施例3(PETG+PBT共重合エラストマーアロイ樹脂、アロイ成分含量:10phr)に対する化粧板のガラス転移温度と弾性率変化を示したグラフであって、Tgは77℃であり、弾性率低下は65℃から始まった。   FIG. 3 is a graph showing a glass transition temperature and a change in elastic modulus of a decorative board with respect to Example 3 (PETG + PBT copolymer elastomer resin, alloy component content: 10 phr), and Tg is 77 ° C. The decrease began at 65 ° C.

図4は実施例4(PETG+PBT共重合エラストマーアロイ樹脂、アロイ成分含量:20phr)に対する化粧板のガラス転移温度と弾性率変化を示したグラフであって、Tgは73℃であり、弾性率低下は60℃から始まった。   FIG. 4 is a graph showing a glass transition temperature and a change in elastic modulus of a decorative board with respect to Example 4 (PETG + PBT copolymer elastomer resin, alloy component content: 20 phr). Tg is 73 ° C. The decrease began at 60 ° C.

図5は比較例(PETG樹脂)に対する化粧板のガラス転移温度と弾性率変化を示したグラフであって、Tgは83℃であり、弾性率低下は73℃から始まった。   FIG. 5 is a graph showing the glass transition temperature and the change in elastic modulus of the decorative board with respect to the comparative example (PETG resin).

本発明によればPETG樹脂にエステル系樹脂またはエラストマー樹脂をアロイすることによって、PETG化粧板の表面品質は維持しつつ成形温度の範囲を広げることができ、また成形可能温度を既存の化粧板との対比で3ないし10℃ほど下げることができる。   According to the present invention, an ester resin or an elastomer resin is alloyed with a PETG resin, so that the range of molding temperature can be expanded while maintaining the surface quality of the PETG decorative board. The temperature can be lowered by about 3 to 10 ° C.

Claims (6)

ポリエチレンテレフタレートグリコール(PETG)樹脂にエステル系樹脂またはエラストマー樹脂を溶融混合したPETGアロイ樹脂を含む化粧板。   A decorative board comprising a PETG alloy resin obtained by melt-mixing an ester resin or an elastomer resin with a polyethylene terephthalate glycol (PETG) resin. PETGアロイ樹脂のガラス転移温度(Tg)が75±3℃であることを特徴とする請求項1に記載の化粧板。   The decorative plate according to claim 1, wherein the glass transition temperature (Tg) of the PETG alloy resin is 75 ± 3 ° C. PETGアロイ樹脂の成形可能な温度範囲が60ないし80℃であることを特徴とする請求項1に記載の化粧板。   The decorative board according to claim 1, wherein the temperature range in which the PETG alloy resin can be molded is 60 to 80 ° C. エステル系樹脂がポリブチレンテレフタレート(PBT)であることを特徴とする請求項1に記載の化粧板。   The decorative board according to claim 1, wherein the ester resin is polybutylene terephthalate (PBT). エラストマー樹脂がポリブチレンテレフタレート樹脂にポリエーテルグリコールを共重合したエラストマー樹脂であることを特徴とする請求項1に記載の化粧板。   2. The decorative board according to claim 1, wherein the elastomer resin is an elastomer resin obtained by copolymerizing a polyether glycol with a polybutylene terephthalate resin. エステル系樹脂またはエラストマー樹脂の混合量がPETG100重量部に対して5ないし20重量部であることを特徴とする請求項1に記載の化粧板。   The decorative board according to claim 1, wherein the mixing amount of the ester resin or the elastomer resin is 5 to 20 parts by weight with respect to 100 parts by weight of PETG.
JP2009546314A 2007-01-23 2008-01-03 PETG-type decorative panel for molding having moldability similar to PVC Pending JP2010516833A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR1020070006824A KR101004614B1 (en) 2007-01-23 2007-01-23 PETG based decorative sheet having forming ability similar with PVC
PCT/KR2008/000025 WO2008091067A1 (en) 2007-01-23 2008-01-03 Petg based decorative sheet having forming ability similar with pvc

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017095699A (en) * 2015-11-23 2017-06-01 株式會社 榮一 Soft PET-G resin composition with improved physical properties

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101294422B1 (en) * 2010-01-08 2013-08-07 (주)엘지하우시스 Method for protecing surface using decoration sheet
KR101248626B1 (en) * 2010-11-12 2013-03-28 (주)엘지하우시스 Eco-friendly deco sheet with excellent formability and printability
KR101244367B1 (en) * 2010-12-09 2013-03-18 웅진케미칼 주식회사 Deco-sheet
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KR102110131B1 (en) * 2018-07-17 2020-05-13 주식회사 케이에스씨 Synthetic resin composition for deco sheets
KR102167904B1 (en) 2018-12-13 2020-10-20 주식회사 케이씨씨 Composition for decoration sheet and decoration sheet prepared therefrom
KR20200035386A (en) 2020-03-25 2020-04-03 이호영 Recyclable laminated fabric
KR20200088259A (en) 2020-07-14 2020-07-22 이호영 A film composition for packaging which is recyclable and excellent in adhesion
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KR20220120900A (en) 2021-02-24 2022-08-31 이호영 Flexible environmentally friendly adhesive film

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002194186A (en) * 2000-12-22 2002-07-10 Mitsubishi Chemicals Corp Decorative polyester resin sheet, its manufacturing method and vessel made of it
JP2002249652A (en) * 2001-02-27 2002-09-06 Mitsubishi Plastics Ind Ltd Sheet for card
JP2003041106A (en) * 2001-05-18 2003-02-13 Mitsubishi Chemicals Corp Copolyester resin composition and stretched film
JP2003231761A (en) * 2002-02-07 2003-08-19 Riken Technos Corp Decorative film and laminated decorative sheet
JP2003246916A (en) * 2001-12-18 2003-09-05 Riken Technos Corp Composition for flexible polyester decorative sheet and the flexible polyester decorative sheet
JP2004075924A (en) * 2002-08-21 2004-03-11 Riken Technos Corp Decorative film and laminated decorative sheet
JP2004091795A (en) * 1998-02-06 2004-03-25 Riken Technos Corp Resin sheet
JP2005298715A (en) * 2004-04-14 2005-10-27 Riken Technos Corp Composition for flexible flame-retardant polyester-based decorative sheet and flexible flame-retardant polyester-based decorative sheet
JP2007246910A (en) * 1998-02-06 2007-09-27 Riken Technos Corp Resin sheet

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3492318B2 (en) * 1998-02-06 2004-02-03 リケンテクノス株式会社 Resin composition and resin sheet
US7081510B2 (en) * 2003-03-12 2006-07-25 Sony Corporation Shell material for recording media
KR100707040B1 (en) * 2003-03-31 2007-04-13 다이니폰 인사츠 가부시키가이샤 Laminate for flooring material
JP2005059416A (en) * 2003-08-13 2005-03-10 Matsushita Electric Works Ltd Manufacturing method for thermoplastic resin formed product
KR100439695B1 (en) * 2003-11-07 2004-07-12 영창실리콘 주식회사 The several layer insulated wire
KR100582338B1 (en) * 2004-01-09 2006-05-22 주식회사 엘지화학 Polyester Resin Compositions with Excellent Heat Resistance and Surface Finish
US20060182911A1 (en) * 2004-10-19 2006-08-17 Tammaji Kulkarni S Gas barrier pet composition for monolayer bottle and process thereof

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004091795A (en) * 1998-02-06 2004-03-25 Riken Technos Corp Resin sheet
JP2007246910A (en) * 1998-02-06 2007-09-27 Riken Technos Corp Resin sheet
JP2002194186A (en) * 2000-12-22 2002-07-10 Mitsubishi Chemicals Corp Decorative polyester resin sheet, its manufacturing method and vessel made of it
JP2002249652A (en) * 2001-02-27 2002-09-06 Mitsubishi Plastics Ind Ltd Sheet for card
JP2003041106A (en) * 2001-05-18 2003-02-13 Mitsubishi Chemicals Corp Copolyester resin composition and stretched film
JP2003246916A (en) * 2001-12-18 2003-09-05 Riken Technos Corp Composition for flexible polyester decorative sheet and the flexible polyester decorative sheet
JP2003231761A (en) * 2002-02-07 2003-08-19 Riken Technos Corp Decorative film and laminated decorative sheet
JP2004075924A (en) * 2002-08-21 2004-03-11 Riken Technos Corp Decorative film and laminated decorative sheet
JP2005298715A (en) * 2004-04-14 2005-10-27 Riken Technos Corp Composition for flexible flame-retardant polyester-based decorative sheet and flexible flame-retardant polyester-based decorative sheet

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017095699A (en) * 2015-11-23 2017-06-01 株式會社 榮一 Soft PET-G resin composition with improved physical properties

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CN101583654B (en) 2012-07-04
EP2121815A4 (en) 2012-02-22

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