KR100522624B1 - Semi-rigid polyurethane foam formulation for automotive interiors - Google Patents
Semi-rigid polyurethane foam formulation for automotive interiors Download PDFInfo
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- KR100522624B1 KR100522624B1 KR10-2003-0006512A KR20030006512A KR100522624B1 KR 100522624 B1 KR100522624 B1 KR 100522624B1 KR 20030006512 A KR20030006512 A KR 20030006512A KR 100522624 B1 KR100522624 B1 KR 100522624B1
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- 239000000203 mixture Substances 0.000 title claims abstract description 31
- 229920005830 Polyurethane Foam Polymers 0.000 title 1
- 238000009472 formulation Methods 0.000 title 1
- 239000011496 polyurethane foam Substances 0.000 title 1
- 239000006260 foam Substances 0.000 claims abstract description 64
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims abstract description 55
- 238000006243 chemical reaction Methods 0.000 claims abstract description 32
- 239000003054 catalyst Substances 0.000 claims abstract description 28
- 229920005862 polyol Polymers 0.000 claims abstract description 23
- 150000003077 polyols Chemical class 0.000 claims abstract description 23
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000000463 material Substances 0.000 claims abstract description 15
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000004971 Cross linker Substances 0.000 claims abstract description 10
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 8
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000002666 chemical blowing agent Substances 0.000 claims abstract description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 8
- 239000012948 isocyanate Substances 0.000 claims abstract description 8
- 150000002513 isocyanates Chemical class 0.000 claims abstract description 8
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 5
- 239000007858 starting material Substances 0.000 claims abstract description 5
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims abstract description 4
- 238000007664 blowing Methods 0.000 claims abstract description 4
- 229960004418 trolamine Drugs 0.000 claims abstract description 4
- 238000006482 condensation reaction Methods 0.000 claims abstract description 3
- 230000000704 physical effect Effects 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 11
- 230000000694 effects Effects 0.000 claims description 6
- 150000001412 amines Chemical group 0.000 claims description 5
- 239000000376 reactant Substances 0.000 claims description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims description 2
- 238000007259 addition reaction Methods 0.000 claims description 2
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 claims description 2
- 229920000638 styrene acrylonitrile Polymers 0.000 claims description 2
- 239000011145 styrene acrylonitrile resin Substances 0.000 claims description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 2
- 235000011187 glycerol Nutrition 0.000 claims 1
- 239000011347 resin Substances 0.000 claims 1
- 229920005989 resin Polymers 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract description 6
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 abstract description 3
- NJTGANWAUPEOAX-UHFFFAOYSA-N molport-023-220-454 Chemical compound OCC(O)CO.OCC(O)CO NJTGANWAUPEOAX-UHFFFAOYSA-N 0.000 abstract description 3
- 238000004904 shortening Methods 0.000 abstract description 3
- 230000006378 damage Effects 0.000 abstract description 2
- 230000014759 maintenance of location Effects 0.000 abstract description 2
- 230000000116 mitigating effect Effects 0.000 abstract description 2
- 230000035484 reaction time Effects 0.000 abstract description 2
- 208000027418 Wounds and injury Diseases 0.000 abstract 1
- 208000014674 injury Diseases 0.000 abstract 1
- 230000007423 decrease Effects 0.000 description 8
- 238000005187 foaming Methods 0.000 description 6
- 230000006866 deterioration Effects 0.000 description 5
- 239000000047 product Substances 0.000 description 4
- 230000009257 reactivity Effects 0.000 description 4
- 230000002411 adverse Effects 0.000 description 3
- 239000012467 final product Substances 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000013589 supplement Substances 0.000 description 2
- 239000004604 Blowing Agent Substances 0.000 description 1
- 206010016654 Fibrosis Diseases 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 230000004761 fibrosis Effects 0.000 description 1
- 239000006261 foam material Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 238000005507 spraying Methods 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4833—Polyethers containing oxyethylene units
- C08G18/4837—Polyethers containing oxyethylene units and other oxyalkylene units
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4833—Polyethers containing oxyethylene units
- C08G18/4837—Polyethers containing oxyethylene units and other oxyalkylene units
- C08G18/485—Polyethers containing oxyethylene units and other oxyalkylene units containing mixed oxyethylene-oxypropylene or oxyethylene-higher oxyalkylene end groups
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
- C08G18/7657—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
- C08G18/7664—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/06—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
본 발명은 차량 내장재의 반경질 우레탄폼 조성물에 관한 것으로 더욱 상세하게는, 차량에 쿠션감을 부여하고 차량 충돌 시 차량 탑승객이 차내에 부딪히는 충격을 흡수, 완화하여 부상을 방지하도록 설치된 인스트루먼트 패널과 헤드레스트, 대시패널, 플로어 콘솔 및 선바이저 등의 다양한 내장재를 구성하는 반경질 우레탄폼을 형성하는데 소요되는 반응시간을 단축시켜 제품생산 사이클을 대폭적으로 줄일 수 있어 생산성 향상에 기여할 수 있는 조성물에 관한 것이다.The present invention relates to a semi-rigid urethane foam composition of the vehicle interior material, and more particularly, the instrument panel and headrest installed to give a cushion feeling to the vehicle and to prevent injury by absorbing and mitigating the impact of the vehicle occupants in the vehicle during a vehicle crash. The present invention relates to a composition that can significantly reduce the production cycle by shortening the reaction time required to form a semi-rigid urethane foam constituting a variety of interior materials, such as dash panels, floor consoles and sun visors, thereby improving productivity.
이를 위하여 본 발명은, 차량 내장재의 반경질 우레탄폼 조성물에 있어서, 글리세린(Glycerin)을 출발물질로 하여 고온 고압의 반응조 내에서 EO/PO(Ethylene Oxide/Propylene Oxide) 부가 반응에 의해 얻어지는 에테르(Ether)계 폴리올(Polyol)로써 말단기의 수산기가 값(OH-Value)이 26~30이고 분자량이 5,000~7,000 정도인 메인 폴리올과, 제품의 경도 유지 및 생산성과 밀접한 트리에탄올 아민(Triethanol Amine)을 배합한 가교제인 크로스 링커(cross linker)와, 블로잉(blowing) 반응 향상과 우레탄폼의 물성 측면 대비 성형성 측면의 특성에 영향을 미치는 제 1촉매제와, 겔(gel) 반응 향상과 우레탄폼의 물성 측면 대비 성형성 측면의 특성에 영향을 미치는 제 2촉매제와, 폼 밀도에 영향을 미치는 화학적 발포제(blowing agent) 및 아닐린(Aniline)과 포르말린(Formalin)의 축합반응에서 얻어진 중간물질을 포스겐(Phosgene)화하여 얻어지는 제품인 중합 MDI를 특정 폴리올과 미리 반응하여 제조된 프레폴리머(prepolymer 또는 변성 MDI)로 NCO 함량이 27중량%인 이소시안산염(Isocyanate)으로 조성된 것 을 특징으로 한다.To this end, the present invention, in the semi-rigid urethane foam composition of the vehicle interior material, using a glycerin (Glycerin) as a starting material ether obtained by the reaction reaction of ethylene oxide (Propylene Oxide) (EO / PO) in a high temperature and high pressure reactor ) As a polyol, a main polyol having a hydroxyl value of 26 to 30 and a molecular weight of 5,000 to 7,000 and a triethanol amine closely related to the hardness retention and productivity of the product are blended. A crosslinker, a crosslinking agent, a first catalyst which affects the blowing reaction and the properties of the moldability compared to the properties of the urethane foam, and the gel reaction and the properties of the urethane foam Intermediate obtained from the condensation reaction of aniline and formalin with a second catalyst that affects the properties of the contrast formability, a chemical blowing agent that affects the foam density, and aniline Prepolymer (modified MDI) prepared by pre-reacting polymerized MDI, which is a product obtained by phosgene-forming phosgene, is composed of isocyanate having an NCO content of 27% by weight. do.
Description
본 발명은 차량 내장재의 반경질 우레탄폼 조성물에 관한 것으로 더욱 상세하게는, 차량에 쿠션감을 부여하고 차량 충돌 시 차량 탑승객이 차내에 부딪히는 충격을 흡수·완화하여 부상을 방지하도록 설치된 인스트루먼트 패널과 헤드레스트, 대시패널, 플로어 콘솔 및 선바이저 등의 다양한 내장재를 구성하는 반경질 우레탄폼을 형성하는데 소요되는 반응시간을 단축시켜 제품생산 사이클을 대폭적으로 줄일 수 있어 생산성 향상에 기여할 수 있는 조성물에 관한 것이다.The present invention relates to a semi-rigid urethane foam composition of the vehicle interior material, and more particularly, the instrument panel and headrest installed to impart a cushion feeling to the vehicle and to prevent injuries by absorbing and mitigating the impact of the vehicle occupants in the vehicle during a vehicle crash. The present invention relates to a composition that can significantly reduce the production cycle by shortening the reaction time required to form a semi-rigid urethane foam constituting a variety of interior materials, such as dash panels, floor consoles and sun visors, thereby improving productivity.
차량 내부에 설치되는 내장재를 구성하는 우레탄폼은 금형에 안치된 패널에 액상의 조성물을 분사한 후 일정 압력과 온도하에서 발포시켜 쿠션성을 띈 발포층으로 변형되는 것인 바, 종래에는 상기와 같이 패널에 발포된 우레탄폼을 형성하기 위한 발포공정에 소요되는 시간이 평균 6~7분 간격의 사이클을 가지고 있었으며, 패널 형성 및 금형에서 탈형된 우레탄폼이 형성된 패널의 잔처리 작업에 소요되는 시간을 합산하면 실제 제품 생산 간격은 10~12분 간격의 사이클을 가지게 되어 제품 생산의 생산성 저하가 심각한 수준이었다.The urethane foam constituting the interior material installed in the vehicle is transformed into a foam layer having a cushioning property by spraying a liquid composition on a panel placed in a mold and then foaming it under a predetermined pressure and temperature. The time required for the foaming process to form the urethane foam foamed in the cycle had an interval of 6 to 7 minutes on average, and the total time for the remaining work of the panel forming and the mold-deformed urethane foam-forming panel was added together. In fact, the actual production intervals had cycles of 10 to 12 minutes, resulting in a severe decrease in productivity.
상기와 같이 생산성이 저하되는 이유로는 액상의 조성물이 발포되어 경화되기 위해 반응하는데 걸리는 시간이 너무 느리게 진행되는 것이 가장 큰 요인으로 작용하고 있으며, 상기와 같이 느린 공정을 타 공정과의 시간에 제품을 생산하는 횟수를 맞추기 위해서는 많은 수의 금형을 따로 설치하여 느린 경화 공정을 양으로 대처하고 있는 실정이다.The reason for the decrease in productivity as described above is that the time taken for the reaction of the liquid composition to foam and harden is too slow, and the main factor is the slow process as described above. In order to meet the number of production, a large number of molds are separately installed to cope with the slow curing process in a positive manner.
그러나, 상기와 같이 많은 수의 금형을 설치하기 위해서는 별도의 생산라인과 그에 따른 인원 확보 및 금형을 설치하기 위한 비용을 부담하여야 하는 문제점이 있었으나 이를 해소할 수 있는 별도의 수단은 제공되지 못하고 있는 실정이다.However, in order to install a large number of molds as described above, there was a problem in that a separate production line and a corresponding number of people secured and costs for installing molds were not provided, but a separate means for solving them was not provided. to be.
본 발명은 상기와 같은 종래의 문제점을 해결하기 위하여 제공된 것으로, 본 발명이 이루고자 하는 기술적 과제는, 쿠션성을 부여하여 탑승자의 안전을 확보하고 소음 흡수 및 쾌적한 차내 환경을 조성하도록 각종 패널에 발포되는 우레탄폼을 형성하는데 소요되는 시간을 대폭적으로 단축시켜 최종 패널의 제조 시간에 소요되는 사이클의 단축을 유발할 수 있어 종래의 발포 금형을 대량으로 설치하여야 하는 설비투자 및 작업에 투입되는 인원을 줄일 수 있도록 하는데 있다.The present invention is provided to solve the above conventional problems, the technical problem to be achieved by the present invention, the urethane foamed to various panels to provide cushioning properties to ensure the safety of the occupants, to absorb noise and create a comfortable in-vehicle environment It greatly reduces the time required to form the foam, which can lead to a shortening of the cycle required for the final panel manufacturing time, thereby reducing the number of equipment investments and labor required for installing a large number of conventional foam molds. have.
이를 위하여 본 발명은, 차량 내장재의 반경질 우레탄폼 조성물에 있어서, 글리세린(Glycerin)을 출발물질로 하여 고온 고압의 반응조 내에서 EO/PO(Ethylene Oxide/Propylene Oxide) 부가 반응에 의해 얻어지는 에테르(Ether)계 폴리올(Polyol)로써 말단기의 수산기가 값(OH-Value)이 26~30이고 분자량이 5,000~7,000 정도인 메인 폴리올과, 제품의 경도 유지 및 생산성과 밀접한 트리에탄올 아민(Triethanol Amine)을 배합한 가교제인 크로스 링커(cross linker)와, 블로잉(blowing) 반응 향상과 우레탄폼의 물성 측면 대비 성형성 측면의 특성에 영향을 미치는 제 1촉매제와, 겔(gel) 반응 향상과 우레탄폼의 물성 측면 대비 성형성 측면의 특성에 영향을 미치는 제 2촉매제와, 폼 밀도에 영향을 미치는 화학적 발포제(blowing agent) 및 아닐린(Aniline)과 포르말린(Formalin)의 축합반응에서 얻어진 중간물질을 포스겐(Phosgene)화하여 얻어지는 제품인 중합 MDI를 특정 폴리올과 미리 반응하여 제조된 프레폴리머(prepolymer 또는 변성 MDI)로 NCO 함량이 27중량%인 이소시안산염(Isocyanate)으로 조성된 것 을 특징으로 한다.To this end, the present invention, in the semi-rigid urethane foam composition of the vehicle interior material, using a glycerin (Glycerin) as a starting material ether obtained by the reaction reaction of ethylene oxide (Propylene Oxide) (EO / PO) in a high temperature and high pressure reactor ) As a polyol, a main polyol having a hydroxyl value of 26 to 30 and a molecular weight of 5,000 to 7,000 and a triethanol amine closely related to the hardness retention and productivity of the product are blended. A crosslinker, a crosslinking agent, a first catalyst which affects the blowing reaction and the properties of the moldability compared to the properties of the urethane foam, and the gel reaction and the properties of the urethane foam Intermediate obtained from the condensation reaction of aniline and formalin with a second catalyst that affects the properties of the contrast formability, a chemical blowing agent that affects the foam density, and aniline Prepolymer (modified MDI) prepared by pre-reacting polymerized MDI, which is a product obtained by phosgene-forming phosgene, is composed of isocyanate having an NCO content of 27% by weight. do.
이하 본 발명에 따른 차량 내장재의 반경질 우레탄폼 조성물에 대한 상세한 설명은 다음과 같다.Hereinafter, a detailed description of the semi-rigid urethane foam composition of the vehicle interior according to the present invention.
본 발명은 차량의 각종 내장재에 사용되는 우레탄폼을 조성하기 위한 우레탄폼 조성물에 관한 것으로, 상기 차량의 각종 내장재에 발포 형성되는 반경질의 우레탄폼을 형성하는데 소요되는 공정시간을 대폭적으로 감축시켜 타공정과의 시간의 갭차를 줄여 원활한 생산이 진행될 수 있으며, 그에 따라 우레탄폼 형성 라인의 확보와 생산라인 시설추가 및 작업인원에 소요되는 공간과 비용을 줄일 수 있도록 하는데 목적이 있다.The present invention relates to a urethane foam composition for forming a urethane foam for use in various interior materials of the vehicle, significantly reducing the process time required to form a urethane foam of the foam formed on the various interior materials of the vehicle to other processes Smooth production can be progressed by reducing the gap between the two and the time. Accordingly, the purpose is to secure a urethane foam forming line, add a production line facility, and reduce the space and cost required for the workforce.
상기와 같은 목적을 달성하기 위해 본 발명은, 자동차의 내부에 장착되는 각종 내장재에 발포되어 충격과 소음을 흡수하고 탑승자에게 편의성을 제공하는 반경질의 우레탄폼을 조성하는 조성물에 있어서, 글리세린(Glycerin)을 출발물질로 하여 고온 고압의 반응조 내에서 EO/PO(Ethylene Oxide/Propylene Oxide) 부가 반응에 의해 얻어지는 에테르(Ether)계 폴리올(Polyol)로써 말단기의 수산기가 값(OH-Value)이 26~30이고 분자량이 5,000~7,000 정도이며 최종 제품인 반경질 우레탄폼을 이루는 기본 물성을 좌우하는 메인 폴리올을 60~65중량% 마련한다.In order to achieve the above object, the present invention, in the composition to form a urethane foam of a radius that is foamed in various interior materials mounted inside the vehicle to absorb shock and noise and provide convenience to the passenger, glycerin (Glycerin) Is an ether-based polyol obtained by EO / PO (Ethylene Oxide / Propylene Oxide) addition reaction in a high temperature and high pressure reaction tank using starting material as the starting material, and the hydroxyl value of the terminal group is 26 ~ It prepares 60-65 wt% of main polyol which is 30 and has a molecular weight of about 5,000 ~ 7,000 and influences the basic physical properties of semi-finished urethane foam.
상기 메인 폴리올은 빠른 반응의 진행과 경화가 가능하도록 조제된 포리올로써 메인 폴리올의 말단 구조내에 PO(Propylene Oxide) 대비 입체 장애 효과가 적은 EO(Ethylene Oxide) Capped 정도를 향상 하므로써 상대 반응물인 NCO의 반응 접근을 용이하게 하여, 빠른 수지화 반응 진행과 전체적인 경화 시간을 단축할 수 있게 조제된 것으로, 생산성과 밀접한 반응성에 영향을 주며 최종 우레탄폼의 경도 및 물성에 영향을 미치게 된다.The main polyol is a polyol prepared to allow rapid reaction progressing and curing, thereby improving the reaction degree of NCO, a relative reactant, by improving the degree of ethylene (Ethylene Oxide) Capped, which is less steric hindrance effect than that of PO (Propylene Oxide) in the terminal polyol terminal structure. It is easy to access, and is prepared to shorten the progress of the rapid resination reaction and the overall curing time, and affects the productivity and reactivity closely and affects the hardness and physical properties of the final urethane foam.
따라서, 상기에서 말단기의 수산기가 값(OH-Value)이나 분자량 및 EO/PO(Ethylene Oxide/Propylene Oxide)의 비율이 상이한 경우 우레탄폼의 경도 및 물성에 영향을 미치므로 원하는 최종 제품을 얻기가 어려우며, 전체에서 차지하는 함량이 65중량%를 초과할 경우에는 우레탄폼의 크랙 또는 부스러짐을 발생하는 원인이되며, 함량이 60중량% 미만일 경우에는 우레탄폼의 형성에 소요되는 시간이 지연되고 우레탄폼의 수축이 심화되어 모양이 뒤틀리며 폼재가 고형화되어 쿠션성이 저하되는 문제점이 발생하므로 배합비율을 엄격히 지켜야 한다.Therefore, when the hydroxyl value of the end group in the above (OH-Value) or molecular weight and EO / PO (Ethylene Oxide / Propylene Oxide) ratio is different affects the hardness and physical properties of the urethane foam it is difficult to obtain the desired final product It is difficult, and if the total content exceeds 65% by weight, it may cause cracking or chipping of the urethane foam.If the content is less than 60% by weight, the time required for the formation of the urethane foam is delayed and Shrinkage is deepened, the shape is distorted, and the foam material is solidified, which causes a problem of deterioration of cushioning properties. Therefore, the mixing ratio must be strictly observed.
그리고, 상기 메인 폴리올에 우레탄폼 분야에서 가교제로써 우레탄폼의 경도 유지와 생산성에 밀접한 관계가 있는 반응성을 조정하는데 주로 사용하는 트리에탄올 아민(Triethanol Amine)인 크로스 링커(Cross Linker)를 0.9~1.4중량% 혼합한다.And 0.9 to 1.4% by weight of a cross linker (Triethanol Amine) mainly used to adjust the reactivity of the main polyol in the urethane foam field as a crosslinking agent closely related to the maintenance of hardness and productivity of urethane foam Mix.
상기 크로스 링커가 전체에서 차지하는 함량이 1.4중량%를 초과할 경우에는 우레탄폼의 경도의 증가 및 의도된 반응성 보다 빠른 반응 진행에 따른 우레탄폼의 밀도 저하에 따른 미충진 현상이 발생되고, 함량이 0.9중량% 미만일 경우에는 경도의 저하 및 반응성의 지연에 따른 생산성 지연과 흐름성 증가에 따른 누액 증가로 성형성이 저하되는 문제점이 발생한다.When the total content of the cross linker exceeds 1.4 wt%, an unfilled phenomenon occurs due to a decrease in the density of the urethane foam due to an increase in hardness of the urethane foam and a faster reaction than the intended reactivity, and a content of 0.9 If less than the weight%, there is a problem in that the moldability is lowered due to the increase in leakage caused by the productivity delay and flowability due to the decrease in hardness and reactivity.
또한, 상기 메인 폴리올과 크로스 링커가 혼합된 혼합물에 블로잉(blowing) 반응 향상 및 반응에 참여하여 폼제에 잔존하여 우레탄폼을 덮는 표피재에 악영향을 미치는 아민의 양을 최소화하여 우레탄폼의 성형성 측면의 특성을 좌우하는 제 1촉매제(반응형 강활성 촉매)를 0.01~0.2중량% 혼합한다.In addition, by improving the blowing reaction and reaction in the mixture of the main polyol and the cross linker, the formability of the urethane foam is minimized by minimizing the amount of amine that remains in the foam agent and adversely affects the skin covering the urethane foam. 0.01 to 0.2% by weight of the first catalyst (reactive strong active catalyst) which determines the properties of the mixture.
상기 제 1촉매제가 차지하는 함량이 0.2중량%를 초과할 경우에는 우레탄폼 형성 반응의 불균형이 발생하여 성형성 저하와 지나친 발포 반응 촉진에 따른 겔(gel) 및 경화가 불안정해지며, 함량이 0.01중량% 미만일 경우에는 우레탄폼 형성 반응의 불균형이 발생하여 성형성 저하와 발포 반응 저하에 따른 밀도 증가 및 물성에 악영향을 끼치게 문제점이 발생하게 된다.When the content of the first catalyst exceeds 0.2% by weight, an imbalance of the urethane foam formation reaction occurs, resulting in unstable gel and curing due to the deterioration of moldability and excessive foaming reaction, and the content is 0.01% by weight. When less than%, an imbalance of the urethane foam forming reaction occurs, thereby causing a problem that adversely affects the increase in density and physical properties due to the deterioration of the moldability and the foaming reaction.
그리고, 상기 메인 폴리올과 크로스 링커 및 제 1촉매제가 혼합된 혼합물에 겔성 향상과 우레탄폼의 물성 측면 대비 성형 측면의 특성을 좌우하고 속성 경화를 위한 물질인 강활성 계열의 제 2촉매제를 0.19~0.5중량% 혼합한다.In addition, 0.19 to 0.5 of the active catalyst-based second catalyst, which is a material for curing the gel and improves the properties of the molding side relative to the physical properties of the urethane foam, and is a property for curing property, in the mixture of the main polyol, the cross linker, and the first catalyst. Mix by weight.
상기 제 2촉매제는 가교제와의 상호 관계를 고려하여 성형성에 문제가 없도록 첨가량을 조정하여야 하며, 제 2촉매제가 차지하는 함량이 0.5중량%를 초과할 경우에는 우레탄폼 형성 반응의 불균형이 발생하여 성형성이 저하되고 겔 반응 촉진에 따른 밀도의 저하 및 반응물의 급격한 점도 변화가 발생하며, 함량이 0.19중량% 미만일 경우에는 우레탄폼 형성 반응의 불균형이 발생하여 성형성이 저하되고 겔 반응의 지연에 따른 의도된 경화 특성을 발휘하지 못하는 문제점이 발생하게 된다.The amount of the second catalyst should be adjusted so that there is no problem in moldability in consideration of the mutual relationship with the crosslinking agent. When the content of the second catalyst exceeds 0.5% by weight, an imbalance of the urethane foam forming reaction occurs and the moldability is increased. This decreases, the density decreases due to the acceleration of the gel reaction, and a sudden change in the viscosity of the reactant occurs. When the content is less than 0.19% by weight, an imbalance of the urethane foam forming reaction occurs, resulting in deterioration of moldability and intention of delaying the gel reaction. The problem of not exhibiting the cured properties is generated.
또한, 상기 메인 폴리올과 크로스 링커, 제 1촉매제 및 제 2촉매제가 혼합된 혼합물에는 우레탄폼의 밀도와 발포 정도를 결정하는 화학적 발포제(Blowing agent)를 1.0~1.5중량% 혼합한다.The main polyol, the cross linker, the first catalyst and the second catalyst are mixed with a 1.0 to 1.5% by weight of a chemical blowing agent (Blowing agent) that determines the density and degree of foaming of the urethane foam.
상기 화학적 발포제는 후술할 상대 재료인 이소시안산염(isocyanate)과의 화학적 반응량인 당량을 고려하여 배합량을 선정하여야 하며, 함량이 1.5중량%를 초과할 경우에는 우레탄폼의 밀도 저하로 인한 물성에 변화를 초래하고 이소시안산염과의 화학적 반응량 차이에 따른 우레탄폼이 딱딱하게 경화되어 수축량 증가의 원인이 되며, 함량이 1.0중량% 미만일 경우에는 우레탄폼의 밀도 증가로 인한 물성의 변화를 초래하는 문제점이 발생한다.The chemical blowing agent should be selected in consideration of the equivalent of the chemical reaction amount with the isocyanate (relative material) to be described later, if the content exceeds 1.5% by weight of the physical properties due to the density decrease of the urethane foam It causes a change and the urethane foam hardens due to the difference in chemical reaction with isocyanate, which causes the increase of shrinkage, and when the content is less than 1.0% by weight, it causes a change in physical properties due to the increase in density of the urethane foam. A problem occurs.
그리고, 상기 메인 폴리올과 크로스 링커, 제 1촉매제, 제 2촉매제 및 화학적 발포제가 혼합된 혼합물에 아닐린(Aniline)과 포르말린(Formalin)의 축합반응에서 얻어진 중간물질을 포스겐(Phosgene)화하여 얻어지는 제품인 중합 MDI를 특정 폴리올과 미리 반응하여 제조된 프레폴리머(prepolymer 또는 변성 MDI)로 NCO 함량이 27중량%이고 빠른 반응에 따른 반응물의 급격한 점도 변화를 방지하여 성형성의 유지 및 물성 만족도를 향상시키기 위한 이소시안산염을 37~30중량% 혼합하여 전체적인 조성이 이루어진다.In addition, the polymerization is a product obtained by phosgene forming an intermediate obtained by condensation of aniline and formalin in a mixture of the main polyol, a cross linker, a first catalyst, a second catalyst and a chemical blowing agent. A prepolymer (prepolymer or modified MDI) prepared by reacting MDI with a specific polyol in advance and has an NCO content of 27% by weight and isocyanate to maintain moldability and improve the satisfaction of physical properties by preventing rapid viscosity change of reactants due to rapid reaction. The total composition is achieved by mixing 37-30% by weight of the acid salt.
상기 이소시안산염은 화학적 발포제와 반응하는 상대 원료로서 말단의 NCO기와 상기 혼합물 중의 수산기(OH기)가 반응하여 우레탄사슬을 형성하는 이액형 원료이며, 함량이 37중량%를 초과할 경우에는 우레탄폼이 딱딱하게 경화되어 수축량 증가의 원인이 되고 점진적인 섬유화 반응에 따른 충진력 저하의 원인이 되며, 함량이 30중량% 미만일 경우에는 우레탄폼의 물성 변화에 따른 전개성능에 악영향을 미치는 한편 우레탄폼이 부스러지기 쉬운 상태가 되는 문제점이 발생한다.The isocyanate is a two-component raw material that reacts with a chemical blowing agent to form a urethane chain by reacting a terminal NCO group with a hydroxyl group (OH group) in the mixture, and when the content exceeds 37% by weight, urethane foam This hardening causes hardening of the shrinkage, and decreases the filling force due to the gradual fibrosis reaction. If the content is less than 30% by weight, it adversely affects the development performance due to the change of the physical properties of the urethane foam, The problem of becoming prone to trouble occurs.
상기에서 제 1촉매제는 본 발명의 목적인 속성 경화를 위해 블로우(blow) 활성이 강한 아민 계열의 촉매를 사용하며, 제 2촉매제는 겔(gel) 및 경화(cure) 활성에 강한 반응형 아민계열 촉매를 사용함이 바람직하다.In the above, the first catalyst is an amine-based catalyst having a strong blow activity for the rapid curing of the object of the present invention, the second catalyst is a reactive amine-based catalyst resistant to gel and cure activity Preference is given to using.
한편, 상기 조성물에는 메인 폴리올과 동일한 방법으로 제조된 말단기의 수산기가 값(OH-Value)이 33~37이며 분자량이 4000~5600 정도이며 메인 폴리올을 보조하여 우레탄폼의 물성과 경화를 보완하고 최종 제품인 우레탄폼의 초기 경화 특성을 향상시키는 물리적으로 균질하게 분산시킨 스틸렌아크로니트릴(SAN)을 전체 중량 대비 0.9~1.4중량%를 선택적으로 혼합하여 제조할 수 있다.On the other hand, in the composition, the hydroxyl value of the end group prepared by the same method as the main polyol (OH-Value) is 33 ~ 37, the molecular weight is about 4000 ~ 5600 and supplements the main polyol to supplement the physical properties and curing of the urethane foam Physically homogeneously dispersed styrene acrylonitrile (SAN) may be prepared by selectively mixing 0.9 to 1.4% by weight with respect to the total weight of the final product to improve the initial curing properties of the urethane foam.
상기 스틸렌아크로니트릴의 함량이 1.4중량%를 초과할 경우에는 경도의 증가와 원가 상승의 요인이 되며, 함량이 0.9중량% 미만일 경우에는 초기 경화성 저하로 인한 생산성의 저하와 제품 탈형 직후 작업자의 부주의한 취급에 의한 불량의 원인이 될 수 있는 문제점이 있다.If the content of the styrene acrylonitrile exceeds 1.4% by weight, it is a factor of increasing the hardness and cost. If the content is less than 0.9% by weight, the productivity is reduced due to the initial hardening deterioration and the worker's carelessness immediately after the product demoulding. There is a problem that may be the cause of failure by handling.
이상에서 살펴본 바와 같은 조성비로 제조된 본 발명에 따른 조성물로 우레탄폼을 형성할 경우 종래에 비해 우레탄폼이 형성되는 시간이 6~7분 정도에서 2분 이내로 대폭 줄어들어 타 공정과의 사이클에 시간을 맞출 수 있으므로 전체적인 제조 공정에 소요되는 시간을 5~6분 정도로 사이클을 단축할 수 있다.When forming the urethane foam with the composition according to the present invention prepared at the composition ratio as described above, the time to form a urethane foam is significantly reduced from 6 to 7 minutes to less than 2 minutes compared to the conventional time to cycle with other processes This allows you to reduce the cycle time from 5 to 6 minutes for the entire manufacturing process.
이상에서 살펴본 바와 같이 본 발명은, 차량의 내부에 설치되는 내장재에 발포되는 반경질의 우레탄폼을 형성하는데 소요되는 시간을 대폭적으로 줄일 수 있어 발포공정을 타 공정과 사이클을 맞출 수 있으므로 종래의 불필요하게 많이 설치해야 하는 발포금형을 줄일 수 있으며, 그에 따라 작업장의 축소와 작업에 투입되는 인력을 줄일 수 있어 원가 절감을 꾀할 수 있는 효과가 있다.As described above, the present invention can significantly reduce the time required to form the urethane foam of the foam to be foamed to the interior material installed inside the vehicle, so that the foaming process can be matched to the cycles of other processes, which is unnecessary in the related art. It is possible to reduce the foam mold that must be installed a lot, thereby reducing the number of workers and the manpower put into the work can reduce the cost.
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
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JPH05287048A (en) * | 1990-04-09 | 1993-11-02 | Polymer Dynamics Technol Inc | Heat-stable polyurethane foam |
KR940004011A (en) * | 1992-08-05 | 1994-03-14 | 존 린들리 렝 | Reaction system for preparing microporous elastomer |
JPH11171963A (en) * | 1997-12-09 | 1999-06-29 | Nippon Polyurethane Ind Co Ltd | Method for producing flexible polyurethane foam |
KR20000032833A (en) * | 1998-11-18 | 2000-06-15 | 정몽규 | Soft polyurethane foam composition |
KR20030090060A (en) * | 2002-05-21 | 2003-11-28 | 덕양산업주식회사 | A composition layer of a instrument panel |
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Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
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JPH05287048A (en) * | 1990-04-09 | 1993-11-02 | Polymer Dynamics Technol Inc | Heat-stable polyurethane foam |
KR940004011A (en) * | 1992-08-05 | 1994-03-14 | 존 린들리 렝 | Reaction system for preparing microporous elastomer |
JPH11171963A (en) * | 1997-12-09 | 1999-06-29 | Nippon Polyurethane Ind Co Ltd | Method for producing flexible polyurethane foam |
KR20000032833A (en) * | 1998-11-18 | 2000-06-15 | 정몽규 | Soft polyurethane foam composition |
KR20030090060A (en) * | 2002-05-21 | 2003-11-28 | 덕양산업주식회사 | A composition layer of a instrument panel |
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