KR101742481B1 - Method for manufacturing composite for filament winding pipe and method for manufacturing filament winding pipe using the same - Google Patents

Method for manufacturing composite for filament winding pipe and method for manufacturing filament winding pipe using the same Download PDF

Info

Publication number
KR101742481B1
KR101742481B1 KR1020140177162A KR20140177162A KR101742481B1 KR 101742481 B1 KR101742481 B1 KR 101742481B1 KR 1020140177162 A KR1020140177162 A KR 1020140177162A KR 20140177162 A KR20140177162 A KR 20140177162A KR 101742481 B1 KR101742481 B1 KR 101742481B1
Authority
KR
South Korea
Prior art keywords
filament winding
manufacturing
resin
winding pipe
polymerization
Prior art date
Application number
KR1020140177162A
Other languages
Korean (ko)
Other versions
KR20160070859A (en
Inventor
하대환
Original Assignee
하대환
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 하대환 filed Critical 하대환
Priority to KR1020140177162A priority Critical patent/KR101742481B1/en
Publication of KR20160070859A publication Critical patent/KR20160070859A/en
Application granted granted Critical
Publication of KR101742481B1 publication Critical patent/KR101742481B1/en

Links

Images

Classifications

    • 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
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/24Crosslinking, e.g. vulcanising, of macromolecules
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C70/00Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
    • B29C70/04Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising reinforcements only, e.g. self-reinforcing plastics
    • B29C70/06Fibrous reinforcements only
    • B29C70/10Fibrous reinforcements only characterised by the structure of fibrous reinforcements, e.g. hollow fibres
    • B29C70/16Fibrous reinforcements only characterised by the structure of fibrous reinforcements, e.g. hollow fibres using fibres of substantial or continuous length
    • 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
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/20Compounding polymers with additives, e.g. colouring
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/10Esters; Ether-esters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/14Peroxides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/04Homopolymers or copolymers of esters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • 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
    • C08L67/06Unsaturated polyesters
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16LPIPES; JOINTS OR FITTINGS FOR PIPES; SUPPORTS FOR PIPES, CABLES OR PROTECTIVE TUBING; MEANS FOR THERMAL INSULATION IN GENERAL
    • F16L11/00Hoses, i.e. flexible pipes
    • F16L11/14Hoses, i.e. flexible pipes made of rigid material, e.g. metal or hard plastics
    • F16L11/16Hoses, i.e. flexible pipes made of rigid material, e.g. metal or hard plastics wound from profiled strips or bands

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Textile Engineering (AREA)
  • Composite Materials (AREA)
  • Moulding By Coating Moulds (AREA)

Abstract

본 발명은 필라멘트 와인딩 파이프용 복합소재 제조방법 및 이에 따른 필라멘트 와인딩용 파이프 제조방법에 관한 것으로서, 더욱 상세하게는 수지와 중합개시제로서의 과산화물에 반응조절제가 첨가되어 혼합됨으로써, 60℃ 이하에서는 수지와 과산화물 사이에 반응조절제가 고르게 분포하여 중합을 원천적으로 막고 있다가 이 온도 이상이 되면 그 순간부터 중합이 개시되어 계절에 관계없이 혼합수지의 온도를 40℃ 정도로 일정하게 유지시키는 동시에 중합은 방지하면서 수지의 점도를 떨어뜨려 보강섬유와의 함침을 촉진시켜 작업성 및 함침불량에 따르는 불량을 최소화 할 수 있으며, 종래에 통상의 방법으로 두꺼운 성형물 성형시 발생하는 고발열에 의한 열수축 현상에 따르는 크랙이나 박리 등의 제품의 하자를 막기 위해 일정 두께로 성형한 후 식힌 뒤, 표면을 샌딩하고 다시 덧대어 성형하는 불편한 공정 및 2차 경화공정 등이 배제되어 공정이 빨라지고, 제품의 생산성 및 제품성이 증가되는 것을 특징으로 한다.The present invention relates to a method for producing a composite material for a filament winding pipe and a method for manufacturing a pipe for filament winding. More particularly, the present invention relates to a method of manufacturing a filament winding pipe by mixing a resin and a peroxide as a polymerization initiator, And the polymerization is initiated from that moment. When the temperature exceeds the above temperature, the temperature of the mixed resin is kept constant at about 40 ° C regardless of the season, and at the same time, The impregnation with the reinforcing fiber is promoted by lowering the viscosity, so that the workability and the defect caused by the poor impregnation can be minimized, and cracks and peeling due to the heat shrinkage phenomenon due to the high heat generated in the conventional molding process In order to prevent defects of the product, After cooling, the back, and inconvenient process and a secondary curing step for forming air sanding the surface and back pad are excluded accelerating the process, characterized in that the increase in the productivity and the product of the product.

Description

필라멘트 와인딩 파이프용 복합소재 제조방법 및 이를 이용한 필라멘트 와인딩용 파이프 제조방법{Method for manufacturing composite for filament winding pipe and method for manufacturing filament winding pipe using the same}FIELD OF THE INVENTION [0001] The present invention relates to a method of manufacturing a filament winding pipe and a method of manufacturing a filament winding pipe using the filament winding pipe,

본 발명은 필라멘트 와인딩 파이프용 복합소재 제조방법 및 이에 따른 필라멘트 와인딩용 파이프 제조방법에 관한 것으로서, 더욱 상세하게는 수지와 중합개시제로서의 과산화물에 반응조절제가 첨가되어 혼합됨으로써, 60℃ 이하에서는 수지와 과산화물 사이에 반응조절제가 고르게 분포하여 중합을 원천적으로 막고 있다가 이 온도 이상이 되면 그 순간부터 중합이 개시되어 계절에 관계없이 혼합수지의 온도를 40℃ 정도로 일정하게 유지시키는 동시에 중합은 방지하면서 수지의 점도를 떨어뜨려 보강섬유와의 함침을 촉진시켜 작업성 및 함침불량에 따르는 불량을 최소화 할 수 있는 필라멘트 와인딩 파이프용 복합소재 제조방법 및 이에 따른 필라멘트 와인딩용 파이프 제조방법에 관한 것이다.
The present invention relates to a method for producing a composite material for a filament winding pipe and a method for manufacturing a pipe for filament winding. More particularly, the present invention relates to a method of manufacturing a filament winding pipe by mixing a resin and a peroxide as a polymerization initiator, And the polymerization is initiated from that moment. When the temperature exceeds the above temperature, the temperature of the mixed resin is kept constant at about 40 ° C regardless of the season, and at the same time, The present invention relates to a method for manufacturing a composite material for a filament winding pipe and a method for manufacturing a filament winding pipe by which impregnation with a reinforcing fiber is promoted by decreasing viscosity to minimize workability and defects due to poor impregnation.

일반적으로 복합소재란 열경화성 또는 열가소성 수지류에 유리섬유나 카본섬유 등의 보강재를 함침시켜 경화제와 열에 의한 경화를 거쳐 형성되는 복합물을 칭하는데, 열경화성 수지류의 대표적인 수지인 불포화 폴리에스테르 수지나 비닐에스테르 수지는 중합개시제로서의 과산화물을 이용하여 중합반응을 개시하는 것이 일반적인 방법이다.Generally, a composite material refers to a composite formed by impregnating a thermosetting or thermoplastic resin with a reinforcing material such as glass fiber or carbon fiber to form a hardening agent and a thermosetting resin. Examples thereof include unsaturated polyester resins and vinyl esters The resin is a general method in which a polymerization reaction is initiated by using a peroxide as a polymerization initiator.

특히 상온용 중합개시제로 많이 사용되는 MEKPO(Methyl Ethyl Ketone Peroxide)의 경우, 수지와 혼합시 성형전 사전 중합을 막기 위해 수지공급업체에서 중합억제제를 첨가하여 공급되는게 일반적이다.In particular, in the case of Methyl Ethyl Ketone Peroxide (MEKPO), which is often used as a polymerization initiator for room temperature, a polymerization inhibitor is generally added to the resin supplier to prevent pre-polymerization before molding.

다만 이 중합억제제는 중합개시제와 혼합시 100% 중합을 억제시키지 못하며 통상은 50% 정도의 억제효과가 있는 것으로 알려져 있다.However, this polymerization inhibitor does not inhibit 100% polymerization when mixed with a polymerization initiator, and it is generally known that it has an inhibitory effect of about 50%.

그런데 수지와 과산화물 혼합시, 성형전부터 이미 사전 중합이 시작되므로 혼합물의 점도가 상승하고 사전 중합반응에 의해 성형후 얻고자 하는 최적의 폴리머 구조를 얻기가 힘들어 물성이 저하된다.However, when the resin and the peroxide are mixed, the pre-polymerization is already started before the molding, so the viscosity of the mixture is increased and it is difficult to obtain the optimum polymer structure to be obtained after pre-polymerization due to the pre-polymerization reaction.

또한, 이렇게 성형된 성형물도 후경화(2차 경화)를 거쳐야 필요로 하는 물성에 도움이 되기 때문에 공정이 길어지고 2차 경화실을 필요로 하는 등의 설비투자가 뒤따른다.In addition, since the molded product thus obtained is also useful for the physical properties required after post-curing (secondary curing), the process is lengthened and equipment investment such as requiring a secondary curing chamber is followed.

특히 동절기에는 과산화물과 혼합되어 공급되는 혼합수지의 점도가 급격히 상승하여 보강섬유 와의 함침이 매우 어려워지고 이에 따른 성형불량 및 물성저하가 나타나게 된다.Especially during the winter season, the viscosity of the mixed resin supplied with the peroxide increases sharply, so that impregnation with the reinforcing fibers becomes very difficult, resulting in poor molding and poor physical properties.

그리고, 통상의 방법으로 두꺼운 성형물 성형시 발생하는 고발열에 의한 열수축 현상에 따르는 크랙이나 박리 등의 제품의 하자를 막기 위해 일정 두께로 성형한 후 식힌 뒤, 표면을 샌딩하고 다시 덧대어 성형해야하기에 불편한 점이 많다.
In order to prevent defects such as cracks or peeling due to thermal shrinkage due to the high heat generated during molding of a thick molded product by a usual method, the molded product should be molded to a predetermined thickness, and then the surface thereof must be sanded and re- There are many inconveniences.

대한민국 공개특허공보 제10-2003-0091120호Korean Patent Publication No. 10-2003-0091120

본 발명은 상기 종래의 문제점을 해소하기 위해 안출된 것으로서,SUMMARY OF THE INVENTION The present invention has been made to solve the above-mentioned problems,

수지와 중합개시제로서의 과산화물에 반응조절제가 첨가되어 혼합됨으로써, 60℃ 이하에서는 수지와 과산화물 사이에 반응조절제가 고르게 분포하여 중합을 원천적으로 막고 있다가 이 온도 이상이 되면 그 순간부터 중합이 개시되어 계절에 관계없이 혼합수지의 온도를 40℃ 정도로 일정하게 유지시키는 동시에 중합은 방지하면서 수지의 점도를 떨어뜨려 보강섬유와의 함침을 촉진시켜 작업성 및 함침불량에 따르는 불량을 최소화 할 수 있는 필라멘트 와인딩 파이프용 복합소재 제조방법 및 이에 따른 필라멘트 와인딩용 파이프 제조방법을 제공하는데 목적이 있다.By adding a reaction modifier to the resin and the peroxide as a polymerization initiator, the reaction regulator is distributed evenly between the resin and the peroxide at temperatures below 60 ° C to prevent polymerization from origin, and when the temperature exceeds the above temperature, , The temperature of the mixed resin is kept constant at about 40 ° C., and the viscosity of the resin is lowered while preventing polymerization, thereby promoting the impregnation with the reinforcing fibers, thereby minimizing defects due to workability and impregnation failure. And a method of manufacturing a pipe for filament winding according to the method.

또한, 종래에 통상의 방법으로 두꺼운 성형물 성형시 발생하는 고발열에 의한 열수축 현상에 따르는 크랙이나 박리 등의 제품의 하자를 막기 위해 일정 두께로 성형한 후 식힌 뒤, 표면을 샌딩하고 다시 덧대어 성형하는 불편한 공정 및 2차 경화공정 등이 배제되어 공정이 빨라지고, 제품의 생산성 및 제품성이 증가되는 필라멘트 와인딩 파이프용 복합소재 제조방법 및 이에 따른 필라멘트 와인딩용 파이프 제조방법을 제공하는데 목적이 있다.
Further, in order to prevent defects such as cracks and peeling due to heat shrinkage due to high heat generated during molding of a thick molded product by a conventional method, the product is molded to a predetermined thickness, cooled, and then the surface is sandblasted and re- The present invention provides a method for manufacturing a composite material for a filament winding pipe in which an uncomfortable process and a secondary curing process are excluded to increase the productivity and productivity of a product, and a method for manufacturing a filament winding pipe.

상기 목적을 달성하고자, 본 발명은 설정온도 이상에서 중합반응이 이루어지는 필라멘트 와인딩 파이프용 복합소재 제조방법 및 이에 따른 필라멘트 와인딩용 파이프 제조방법에 있어서,In order to accomplish the above object, the present invention provides a method for manufacturing a composite material for a filament winding pipe in which a polymerization reaction occurs at a set temperature or higher, and a method for manufacturing a filament winding pipe,

수지 100 중량부에 중합개시제로서의 과산화물 0.5 ~ 1.5 중량부와 반응조절제 0.1 ~ 10 중량부를 혼합하여 경화하는 것을 특징으로 하는 필라멘트 와인딩 파이프용 복합소재 제조방법 및 이에 따른 필라멘트 와인딩용 파이프 제조방법에 관한 것이다.
Wherein 0.5 to 1.5 parts by weight of a peroxide as a polymerization initiator and 0.1 to 10 parts by weight of a reaction modifier are mixed and cured in 100 parts by weight of the resin, and a method for manufacturing a filament winding pipe .

이상에서 살펴 본 바와 같이, 본 발명의 필라멘트 와인딩 파이프용 복합소재 제조방법 및 이에 따른 필라멘트 와인딩용 파이프 제조방법은 수지와 중합개시제로서의 과산화물에 반응조절제가 첨가되어 혼합됨으로써, 60℃ 이하에서는 수지와 과산화물 사이에 반응조절제가 고르게 분포하여 중합을 원천적으로 막고 있다가 이 온도 이상이 되면 그 순간부터 중합이 개시되어 계절에 관계없이 혼합수지의 온도를 40℃ 정도로 일정하게 유지시키는 동시에 중합은 방지하면서 수지의 점도를 떨어뜨려 보강섬유와의 함침을 촉진시켜 작업성 및 함침불량에 따르는 불량을 최소화 할 수 있는 효과가 있다.As described above, in the method for manufacturing a composite material for a filament winding pipe of the present invention and the method for manufacturing a pipe for filament winding according to the present invention, a reaction regulator is added to peroxide as a resin and a polymerization initiator, And the polymerization is initiated from that moment. When the temperature exceeds the above temperature, the temperature of the mixed resin is kept constant at about 40 ° C regardless of the season, and at the same time, The viscosity is lowered to promote the impregnation with the reinforcing fibers, and the workability and defects due to poor impregnation can be minimized.

또한, 종래에 통상의 방법으로 두꺼운 성형물 성형시 발생하는 고발열에 의한 열수축 현상에 따르는 크랙이나 박리 등의 제품의 하자를 막기 위해 일정 두께로 성형한 후 식힌 뒤, 표면을 샌딩하고 다시 덧대어 성형하는 불편한 공정 및 2차 경화공정 등이 배제되어 공정이 빨라지고, 제품의 생산성 및 제품성이 증가되는 효과가 있다.
Further, in order to prevent defects such as cracks and peeling due to heat shrinkage due to high heat generated during molding of a thick molded product by a conventional method, the product is molded to a predetermined thickness, cooled, and then the surface is sandblasted and re- An uncomfortable process and a secondary curing process are excluded so that the process is speeded up, and productivity and productability of the product are increased.

도 1은 본 발명의 일실시예에 따른 반응조절제의 메카니즘을 나타낸 개략도이고,
도 2는 본 발명의 일실시예에 따른 필라멘트 와인딩용 파이프 제조방법을 나타낸 순서도이다.
1 is a schematic view showing a mechanism of a reaction control agent according to an embodiment of the present invention,
2 is a flowchart illustrating a method of manufacturing a filament winding pipe according to an embodiment of the present invention.

이와 같은 특징을 갖는 본 발명은 그에 따른 바람직한 실시예를 통해 더욱 명확히 설명될 수 있을 것이다.The present invention having such characteristics can be more clearly described by the preferred embodiments thereof.

이하 첨부된 도면을 참조로 본 발명의 여러 실시예들을 상세히 설명하기 전에, 다음의 상세한 설명에 기재되거나 도면에 도시된 구성요소들의 구성 및 배열들의 상세로 그 응용이 제한되는 것이 아니라는 것을 알 수 있을 것이다. 본 발명은 다른 실시예들로 구현되고 실시될 수 있고 다양한 방법으로 수행될 수 있다. 또, 장치 또는 요소 방향(예를 들어 "전(front)", "후(back)", "위(up)", "아래(down)", "상(top)", "하(bottom)", "좌(left)", "우(right)", "횡(lateral)")등과 같은 용어들에 관하여 본원에 사용된 표현 및 술어는 단지 본 발명의 설명을 단순화하기 위해 사용되고, 관련된 장치 또는 요소가 단순히 특정 방향을 가져야 함을 나타내거나 의미하지 않는다는 것을 알 수 있을 것이다. 또한, "제 1(first)", "제 2(second)"와 같은 용어는 설명을 위해 본원 및 첨부 청구항들에 사용되고 상대적인 중요성 또는 취지를 나타내거나 의미하는 것으로 의도되지 않는다.DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Before describing in detail several embodiments of the present invention with reference to the accompanying drawings, it is to be understood that the invention is not limited to the details of construction and the arrangement of the components described in the following detailed description or illustrated in the drawings will be. The invention may be embodied and carried out in other embodiments and carried out in various ways. It should also be noted that the device or element orientation (e.g., "front," "back," "up," "down," "top," "bottom, Expressions and predicates used herein for terms such as "left," " right, "" lateral, " and the like are used merely to simplify the description of the present invention, Or that the element has to have a particular orientation. Also, terms such as " first "and" second "are used herein for the purpose of the description and the appended claims, and are not intended to indicate or imply their relative importance or purpose.

따라서, 본 명세서에 기재된 실시예와 도면에 도시된 구성은 본 발명의 가장 바람직한 일 실시예에 불과할 뿐이고 본 발명의 기술적 사상을 모두 대변하는 것은 아니므로, 본 출원시점에 있어서 이들을 대체할 수 있는 다양한 균등물과 변형예들이 있을 수 있음을 이해하여야 한다.Therefore, the embodiments described in this specification and the configurations shown in the drawings are merely the most preferred embodiments of the present invention and do not represent all the technical ideas of the present invention. Therefore, It is to be understood that equivalents and modifications are possible.

도 1은 본 발명의 일실시예에 따른 반응조절제의 메카니즘을 나타낸 개략도이다.1 is a schematic view showing the mechanism of a reaction control agent according to an embodiment of the present invention.

도 1에 도시한 바와 같이, 본 발명의 필라멘트 와인딩 파이프용 복합소재 제조방법 및 이에 따른 필라멘트 와인딩용 파이프 제조방법은 열경화성 또는 열가소성 수지류에 유리섬유나 카본섬유 등의 보강재를 함침시켜 경화제와 열에 의한 경화를 거쳐 형성되는 복합물을 칭하는데, 열경화성 수지류의 대표적인 수지인 불포화 폴리에스테르 수지나 비닐에스테르 수지는 중합개시제로서의 과산화물을 이용하여 중합반응이 이루어져 복합소재가 제조된다.As shown in FIG. 1, the method for manufacturing a composite material for a filament winding pipe according to the present invention and the method for manufacturing a filament winding pipe according to the present invention include the steps of impregnating a thermosetting or thermoplastic resin with a reinforcing material such as glass fiber or carbon fiber, The unsaturated polyester resin or vinyl ester resin, which is a representative resin of thermosetting resin streams, is subjected to a polymerization reaction using a peroxide as a polymerization initiator to produce a composite material.

여기에 반응조절제가 수지와 중합개시제 사이에 고르게 분포하여 60℃ 이하에서 중합을 원천적으로 막고 있다가 60℃ 이상이 되면 그 순간부터 중합이 개시되는 원리로써, 도 1에서처럼, 과산화물(Initiator) 경화개시형 수지(불포화 폴리에스테르 혹은 비닐에스테르)의 반응조절제(BB) 작용 메카니즘은 40℃ 아래에서는 중합이 일어나지 않도록 수지의 끝단에 위치하다가 약 60℃ 시점에서 반응조절제가 빠지면서 중합이 개시되는 원리이다.Here, as a principle in which polymerization of the reaction control agent is uniformly distributed between the resin and the polymerization initiator and the polymerization is originally blocked at 60 ° C or lower, and when the temperature is 60 ° C or higher, polymerization starts from that moment. As shown in FIG. 1, initiation of initiator curing (BB) action mechanism of the resin (unsaturated polyester or vinyl ester) is positioned at the end of the resin so that polymerization does not occur at 40 ° C or lower, and polymerization is started when the reaction regulator is removed at about 60 ° C.

여기서, 상기 복합소재는 수지 100 중량부에 과산화물 0.5 ~ 1.5 중량부와 반응조절제 0.1 ~ 10 중량부를 혼합하여 경화되는 것이다.Here, the composite material is cured by mixing 0.5 to 1.5 parts by weight of peroxide and 0.1 to 10 parts by weight of a reaction modifier with 100 parts by weight of the resin.

그리고, 상기 수지는 비닐에스테르 수지, 에폭시 수지, 불포화 폴리에스테르 수지 중 어느 하나를 선택적으로 사용한다.Any one of a vinyl ester resin, an epoxy resin, and an unsaturated polyester resin is selectively used as the resin.

또한, 상기 반응조절제는 2-부텐디오익산 (2Z)-디부틸에스터(2-Butenedioic acid (2Z)-dibutyl ester)로 이루어진다. 이때, 상기 2-부텐디오익산 (2Z)-디부틸에스터(2-Butenedioic acid (2Z)-dibutyl ester) 100 중량부에 니트록사이드, 1-(디에톡시포스피닐)-2,2-디메틸프로필 1,1-디메틸에틸(Nitroxide, 1-(diethoxyphosphinyl)-2,2-dimethylpropyl 1,1-dimethylethyl) 3 ~ 8 중량부가 포함된다.In addition, the reaction modifier is composed of 2-butenedioic acid (2Z) -dibutyl ester. At this time, 100 parts by weight of the 2-butenedioic acid (2Z) -dibutyl ester was added to 100 parts by weight of nitric oxide, 1- (diethoxyphosphinyl) -2,2-dimethylpropyl And 3 to 8 parts by weight of 1,1-dimethylethyl (Nitroxide, 1- (diethoxyphosphinyl) -2,2-dimethylpropyl 1,1-dimethylethyl).

하기에서는 상기 반응조절제의 [화학식 1]을 기술한다.In the following, the formula (1) of the reaction modifier is described.

Figure 112014119933500-pat00001
Figure 112014119933500-pat00001

상기의 [화학식 1]은 2-부텐디오익산 (2Z)-디부틸에스터(2-Butenedioic acid (2Z)-dibutyl ester)의 화학식이다.The above formula (1) is a formula of 2-butenedioic acid (2Z) -dibutyl ester.

Figure 112014119933500-pat00002
Figure 112014119933500-pat00002

상기의 [화학식 2]는 니트록사이드, 1-(디에톡시포스피닐)-2,2-디메틸프로필 1,1-디메틸에틸(Nitroxide, 1-(diethoxyphosphinyl)-2,2-dimethylpropyl 1,1-dimethylethyl)의 화학식이다.
The above-mentioned formula (2) can be prepared by reacting nitrile, 1- (diethoxyphosphinyl) -2,2-dimethylpropyl 1,1-dimethylethyl, dimethylethyl).

한편, 본 발명의 복합소재 경화는 필라멘트 와인딩 공정에 적용되나 그 외 이송성형, 진공성형, 인발등 거의 모든 공정에 유효하다. 이때, 필라멘트 와인딩 공정의 경우, 상기 개요처럼 수지로 함침된 보강재가 몰드나 만드렐 위에 닿을시 그 닿는 부위에 70℃ 정도의 열원(히터나 적외선 램프 등)을 가하여 그 순간부터 중합이 개시 되도록 함에 따라 사전중합 없이 중합됨으로서 중합에 의한 폴리머 가교가 극대화 되어 탁월한 물성의 복합물이 성형된다.On the other hand, the composite material curing of the present invention is applied to the filament winding process, but it is effective for almost all processes such as transfer molding, vacuum molding, and drawing. At this time, in the filament winding process, when a stiffener impregnated with resin is touched on a mold or a mandrel, a heat source (heater, infrared lamp, etc.) of about 70 캜 is applied to initiate polymerization from the moment Accordingly, the polymer is crosslinked without pre-polymerization, thereby maximizing polymer crosslinking by polymerization and molding a composite having excellent physical properties.

또한 이렇게 함으로써 상기 기존 시스템에 의한 2차 경화도 배제되는 결과가 나오므로 공정이 빨라지고 공간활용이 극대화 된다.In addition, since the secondary curing by the existing system is also eliminated, the process is speeded up and the space utilization is maximized.

특히 동절기 성형시는 그 효과가 훨씬 기존법보다 나아지게 되며, 또한 통상의 방법으로 두꺼운 성형물 성형시 발생하는 고발열에 의한 열수축 현상에 따르는 크랙이나 박리등의 제품의 하자를 막기 위해 일정 두께 성형후 식힌후 표면을 샌딩하고 다시 덧대어 성형하는 불편함이 해결된다.In particular, in winter season, the effect is much better than the conventional method. In addition, in order to prevent defects such as cracks and peeling due to heat shrinkage due to the high heat generated when molding a thick product by a usual method, The inconvenience of sanding and re-pouring the posterior surface is solved.

이렇게 선택적 반응온도 조절형으로 성형시 불포화 폴리에스테르류 수지로도 강력한 에폭시 물성을 냄으로써 공정이 길고, 비싼 에폭시 수지를 쓰지 않고도 에폭시 물성을 얻을 수 있다.
By this selective reaction temperature control type, it is possible to obtain epoxy physical properties without using expensive epoxy resin by making strong epoxy property even with unsaturated polyester resin when forming.

이하에서는 본 발명의 제조방법이 적용된 비닐에스테르 수지와 에폭시 수지 비교에 대한 [표 1]과 [표 2]을 기술한다.[Table 1] and [Table 2] for comparison of vinyl ester resin and epoxy resin to which the production method of the present invention is applied will be described below.

항목Item 에폭시수지Epoxy resin 비닐에스터수지Vinyl ester resin 혼합비Mixing ratio 100:25~30100: 25-30 100:0.5~1.5100: 0.5 to 1.5 점도Viscosity 약 1,000 cpsApproximately 1,000 cps 약 300~400 cps300 to 400 cps 저점도Low viscosity 비중importance 약 1.11Approximately 1.11 약 1.05Approximately 1.05 약 5% 낮음About 5% less 겔화시간Gel time 약 70분About 70 minutes 약 35분About 35 minutes 50% 짧음50% short 최고발열온도Maximum heat temperature 210210 150~200150 ~ 200 5~25% 낮음5 to 25% less 인장강도 psiTensile strength psi 10,70010,700 12,00012,000 +12% 높음+ 12% higher 파단박리 인장율Breaking Tensile Ratio 4.1%4.1% 7.5%7.5% +83% 높음+ 83% higher 인장탄성 psiTensile elastic psi 493,000493,000 540,000540,000 +10%+ 10% 굴곡강도 psiFlexural strength psi 18,00018,000 22,00022,000 +22% 높음+ 22% higher 굴곡탄성 psiFlexural elasticity psi 493,000493,000 500,000500,000 +1% 높음+ 1% high 열변형온도Heat distortion temperature 7979 108108 +37%+ 37%

수지Suzy 경화온도Curing temperature 반응조절제 유무Presence or absence of reaction modifier 탄성계수,GPaElastic modulus, GPa 열변형온도 Tg,Thermal deformation temperature Tg, 비닐에스테르1Vinyl ester 1 상온Room temperature radish 55 121121 비닐에스테르2Vinyl ester 2 상온Room temperature radish 77 120120 비닐에스테르1Vinyl ester 1 상온Room temperature 반응억제제 첨가Addition of inhibitor 99 115115 비닐에스테르2Vinyl ester 2 가열heating 반응조절제 첨가Addition of reaction modifier 8.58.5 127127 비닐에스테르1Vinyl ester 1 가열heating 반응조절제 첨가Addition of reaction modifier 1616 121121

*가열경화조건 : 수지온도 40℃/몰드온도 70℃* Heat curing condition: Resin temperature 40 ℃ / Mold temperature 70 ℃

상기 [표 2]에서 보듯이 비닐에스테르1의 경우 탄성계수가 일반경화시 보다 2배 이상으로 에폭시 물성 이상을 보이는 것을 알수 있다.
As shown in the above Table 2, it can be seen that the elastic modulus of the vinyl ester 1 is more than twice the epoxy physical property as that of the general curing.

이하에서는 상기에서 기술한 필라멘트 와인딩 파이프용 복합소재 제조방법에 의해 제조된 복합소재를 이용한 필라멘트 와인딩용 파이프 제조방법에 대해 도면을 참고하여 기술한다.Hereinafter, a method for manufacturing a filament winding pipe using a composite material manufactured by the composite material manufacturing method for a filament winding pipe will be described with reference to the drawings.

도 2는 본 발명의 일실시예에 따른 필라멘트 와인딩용 파이프 제조방법을 나타낸 순서도이다.2 is a flowchart illustrating a method of manufacturing a filament winding pipe according to an embodiment of the present invention.

도 2에 도시한 바와 같이, 본 발명의 필라멘트 와인딩용 파이프 제조방법은 우선, 상기의 복합소재로 이루어진 판재를 필라멘트 와인딩하는데, 이때, 맨드릴(mandrel) 장치에 의해 판재를 필라멘트 와인딩 공정이 이루어진다(S100).As shown in FIG. 2, in the filament winding pipe manufacturing method of the present invention, a filament winding process is performed on a plate made of the composite material by a mandrel device (S100 ).

이렇게, 상기 필라멘트 와인딩에 따라 복합소재의 판재가 나선형으로 말리면서 파이프 형태로 형성되는데, 이때, 상기 나선형의 판재는 상호 중첩되는 부위가 발생하고, 이 부위에 70℃ 이상의 열원을 가열하면 순간 경화한다(S200). 이때, 상기 순간 경화되는 방식은 상기에서 복합소재 제조방법에 기술되어 있기에 참고한다.The spiral plate members are overlapped with each other. When the heat source of 70 ° C or more is heated, the spiral plate members are cured instantaneously (S200). At this time, the instant curing method is described in the composite material manufacturing method described above.

여기서, 상기 필라멘트 와인딩에 따라 복합소재의 판재가 상호 중첩되는 부위에는 히터, 적외선 램프, 열풍기 중 어느 하나를 이용하여 가열한다.Here, a portion where the plate materials of the composite material are overlapped with each other according to the filament winding is heated by using a heater, an infrared lamp, or a hot air heater.

이때, 상기 히터, 적외선 램프, 열풍기 등을 대차위에 고정 설치하여 이동 가능하고, 그로 인해, 복합소재의 판재가 상호 중첩되는 부위에 맞춰 이동할 수 있어 작업하기가 편리하다.At this time, the heater, the infrared lamp, the hot air blower, and the like can be fixedly installed on the carriage and moved, so that the plate material of the composite material can move according to the area where the plates are overlapped with each other.

이렇게, 완성된 파이프에서 맨드릴장치를 이탈시켜 완료한다(S300).In this way, the mandrel device is removed from the completed pipe and completed (S300).

Claims (6)

수지 100 중량부에 중합개시제로서 과산화물 0.5 ~ 1.5 중량부와 제 1 반응조절제 0.1 ~ 10 중량부를 혼합하여 경화하는 것을 특징으로 하는 필라멘트 와인딩 파이프용 복합소재 제조방법으로서,
상기 제 1 반응조절제에 의해 40℃ 이하에서는 중합이 방지되면서 60℃ 이상에서 중합이 이루어지며,
상기 수지는 비닐에스테르 수지이며,
상기 제 1 반응조절제는 2-부텐디오익산 (2Z)-디부틸에스터(2-Butenedioic acid (2Z)-dibutyl ester)이고,
상기 제 1 반응조절제 100 중량부에 대해 제 2 반응조절제로서 3 ~ 8 중량부의 니트록사이드, 1-(디에톡시포스피닐)-2,2-디메틸프로필 1,1-디메틸에틸(Nitroxide, 1-(diethoxyphosphinyl)-2,2-dimethylpropyl 1,1-dimethylethyl)를 추가로 혼합하는 것을 특징으로 하는 필라멘트 와인딩 파이프용 복합소재 제조방법.
Characterized in that 0.5 to 1.5 parts by weight of peroxide as a polymerization initiator and 0.1 to 10 parts by weight of a first reaction modifier are mixed and cured in 100 parts by weight of the resin,
By the first reaction control agent, polymerization is prevented at 40 ° C or lower, and polymerization is carried out at 60 ° C or higher,
The resin is a vinyl ester resin,
The first reaction modifier is 2-butenedioic acid (2Z) -dibutyl ester,
3 to 8 parts by weight of a nitroxide, 1- (diethoxyphosphinyl) -2,2-dimethylpropyl 1,1-dimethylethyl (1-n-butyllithium) as a second reaction controlling agent to 100 parts by weight of the first reaction- (diethoxyphosphinyl) -2,2-dimethylpropyl 1,1-dimethylethyl) is further mixed.
삭제delete 삭제delete 삭제delete 삭제delete 삭제delete
KR1020140177162A 2014-12-10 2014-12-10 Method for manufacturing composite for filament winding pipe and method for manufacturing filament winding pipe using the same KR101742481B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1020140177162A KR101742481B1 (en) 2014-12-10 2014-12-10 Method for manufacturing composite for filament winding pipe and method for manufacturing filament winding pipe using the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1020140177162A KR101742481B1 (en) 2014-12-10 2014-12-10 Method for manufacturing composite for filament winding pipe and method for manufacturing filament winding pipe using the same

Publications (2)

Publication Number Publication Date
KR20160070859A KR20160070859A (en) 2016-06-21
KR101742481B1 true KR101742481B1 (en) 2017-06-02

Family

ID=56353545

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1020140177162A KR101742481B1 (en) 2014-12-10 2014-12-10 Method for manufacturing composite for filament winding pipe and method for manufacturing filament winding pipe using the same

Country Status (1)

Country Link
KR (1) KR101742481B1 (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001205711A (en) 2000-01-25 2001-07-31 Sekisui Chem Co Ltd Manufacturing method for thermosetting resin pipe and manufacturing method for frp composite pipe
KR100322244B1 (en) 1993-03-24 2002-07-27 록타이트 코오포레이션 Textile / Resin Composites and Methods for Making the Same

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030091120A (en) 2002-05-22 2003-12-03 박재형 A method of embedding waste to be treated by mixing a reaction regulator and inoculation strains with synthetic resin film.

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100322244B1 (en) 1993-03-24 2002-07-27 록타이트 코오포레이션 Textile / Resin Composites and Methods for Making the Same
JP2001205711A (en) 2000-01-25 2001-07-31 Sekisui Chem Co Ltd Manufacturing method for thermosetting resin pipe and manufacturing method for frp composite pipe

Also Published As

Publication number Publication date
KR20160070859A (en) 2016-06-21

Similar Documents

Publication Publication Date Title
CN106626662B (en) Sandwich structure composite material and preparation method thereof
US2433643A (en) Process of treating phenolic sheet
TW201533109A (en) One-shot production of composites
JP6562153B2 (en) FIBER-REINFORCED COMPOSITE MOLDED ARTICLE AND METHOD FOR PRODUCING THE SAME
KR101742481B1 (en) Method for manufacturing composite for filament winding pipe and method for manufacturing filament winding pipe using the same
KR20170055616A (en) Prepreg, composites and method for manufacturing the same
US3029473A (en) Vacuum post-curing of infusible plastic material
US10272620B2 (en) Fiber-reinforced composite material and method for manufacturing same
JP6342012B2 (en) Method for producing thermoplastic prepreg and thermoplastic prepreg produced thereby
EP3521008B1 (en) Mold for manufacturing slab and manufacturing method thereof
WO2012157327A1 (en) Resin transfer molding method and resin transfer molding device
TWI791513B (en) Sheet winding (sheet winding) forming method
JP2020176239A (en) Epoxy resin composition, prepreg, method for producing prepreg, and method for producing fiber-reinforced composite material
US9469055B2 (en) Curing composite materials comprising latent-cure resins
KR101694126B1 (en) Method of Curing Run Flat Tire
CN109940908A (en) A kind of moulding process of carbon fiber and phenolic resin composite
KR102042175B1 (en) Method for manufacturing artificial marble, artificial marble prepared thereby, and artificial marble structure using the same
KR100582566B1 (en) The multiplex pultrusion method with dielectric heating device
CN113045859A (en) Low-temperature curing epoxy resin-based prepreg with long storage period and preparation method thereof
KR101725523B1 (en) Process Of Producing Carbon Fiber Prepreg And Process Of Producing Carbon Fiber Thrmoplastic Composite Using PhotoThermosetting
US2449390A (en) Process for the production of hard rubber
CN113563695B (en) Epoxy resin modified curing process and thermosetting epoxy resin compound
JPS6015431A (en) Solid-phase curing of solid epoxy resin molding
CN207465478U (en) A kind of Novel rapid-heating and the quartz water tank die of cooling
KR102188158B1 (en) Method of manufacturing golf shaft with definited external diameter

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
E701 Decision to grant or registration of patent right
GRNT Written decision to grant