KR100877872B1 - A manufacturing method of recycled resin using resin scrap - Google Patents

A manufacturing method of recycled resin using resin scrap Download PDF

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KR100877872B1
KR100877872B1 KR20070002484A KR20070002484A KR100877872B1 KR 100877872 B1 KR100877872 B1 KR 100877872B1 KR 20070002484 A KR20070002484 A KR 20070002484A KR 20070002484 A KR20070002484 A KR 20070002484A KR 100877872 B1 KR100877872 B1 KR 100877872B1
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resin
extruder
temperature
melt
new material
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KR20080065393A (en
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한길성
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한길성
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B9/00Making granules
    • B29B9/02Making granules by dividing preformed material
    • B29B9/06Making granules by dividing preformed material in the form of filamentary material, e.g. combined with extrusion
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B13/00Conditioning or physical treatment of the material to be shaped
    • B29B13/02Conditioning or physical treatment of the material to be shaped by heating
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B13/00Conditioning or physical treatment of the material to be shaped
    • B29B13/04Conditioning or physical treatment of the material to be shaped by cooling
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B17/00Recovery of plastics or other constituents of waste material containing plastics
    • B29B17/04Disintegrating plastics, e.g. by milling
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B17/00Recovery of plastics or other constituents of waste material containing plastics
    • B29B17/04Disintegrating plastics, e.g. by milling
    • B29B2017/0424Specific disintegrating techniques; devices therefor
    • B29B2017/0468Crushing, i.e. disintegrating into small particles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B17/00Recovery of plastics or other constituents of waste material containing plastics
    • B29B17/04Disintegrating plastics, e.g. by milling
    • B29B2017/0424Specific disintegrating techniques; devices therefor
    • B29B2017/0496Pyrolysing the materials
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/62Plastics recycling; Rubber recycling

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  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Environmental & Geological Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Abstract

본 발명은 발포상의 수지 스크랩(scrap)을 해가교하여 얻어지는 재생수지의 제조방법에 관한 것으로, 본 발명의 제조방법에 의하여 제조된 재생수지는 재생수지 자체의 포장 및 보관상의 우수성뿐만 아니라, 그 물성이 신소재 수지와 유사하여 제품에 다량으로 첨가되더라도 신소재 수지만을 사용한 제품과 동등한 정도의 물성을 나타내어 경제적인 측면에서 우수한 효과가 있다.The present invention relates to a method for producing recycled resin obtained by crosslinking foamed resin scrap, and the recycled resin produced by the method of the present invention is not only superior in terms of packaging and storage of the recycled resin itself, but also its physical properties. Similar to the new material resin, even if it is added to the product in large quantities, it exhibits the same physical properties as the product using only the new material resin, and thus has an excellent economical effect.

재생수지, 해가교, 펠렛, 신발 중창 Recycling Resin, Sea Bridge, Pellets, Shoe Midsole

Description

수지 스크랩을 이용한 재생수지 제조방법{A MANUFACTURING METHOD OF RECYCLED RESIN USING RESIN SCRAP}Recycling resin manufacturing method using resin scrap {A MANUFACTURING METHOD OF RECYCLED RESIN USING RESIN SCRAP}

도 1은 재생수지 제조방법의 순서도를 나타낸다.1 shows a flowchart of a method for producing recycled resin.

도 2는 재생수지 제조장치의 모식도를 나타낸다.2 shows a schematic view of a recycled resin production apparatus.

도 3은 2차 압출기의 배출부에 부착된 원판의 사시도를 나타낸다.3 shows a perspective view of a disc attached to the outlet of a secondary extruder.

도 4는 본 발명의 제조방법에 의하여 제조된 재생수지를 나타낸 사진이다.Figure 4 is a photograph showing a recycled resin produced by the manufacturing method of the present invention.

<부호의 설명><Description of the code>

1---원판 2---통공1 --- disc 2 --- hole

본 발명은 발포상의 수지 스크랩(scrap)을 해가교하여 얻어지는 재생수지의 제조방법에 관한 것으로, 보다 상세하게는 수지 발포체 스크랩을 고온에서 1차 해가교시켜 용융물을 얻고, 상기 용융물을 2차 해가교시켜 펠렛(pellet)화된 재생수지를 얻는 방법에 관한 것이다.The present invention relates to a method for producing recycled resin obtained by crosslinking foamed resin scrap, and more particularly, to melt melt by primary crosslinking of a resin foam scrap at a high temperature, and to crosslink the melt secondaryly. The present invention relates to a method for obtaining pelletized recycled resin.

가교화(cross-linking)된 수지, 예를 들어 에틸렌 비닐아세테이트(EVA) 및/또는 폴리에틸렌(PE) 발포체 등을 주원료로 하여 제조된 신발 중창, 신발 안창, 건 축용 층별단열제 및 자동차 부품 등의 각종 수지 제품 및 이들 제품의 제조시 발생된 스크랩 등은 재활용 기술이 완전히 개발되어 있지 않아 단순히 소각하여 열원으로 이용하거나, 파쇄하여 타용도로 사용하거나, 또는 일부의 경우 강제 압착 롤링으로 시트화하여 재생수지로서 사용하여 왔다.Such as shoe midsoles, shoe insoles, layered insulations for automobiles, and automobile parts manufactured from cross-linked resins such as ethylene vinyl acetate (EVA) and / or polyethylene (PE) foam Various resin products and scraps generated during the manufacture of these products are not completely developed for recycling, so they are simply incinerated and used as a heat source, or crushed for other purposes, or in some cases sheeted by forced compression rolling to be recycled. It has been used as a resin.

상기 용도 중, 시트화하여 사용하는 재생수지는 시트형상이므로 부피가 커져서 포장의 어려움이 있으며, 운반이나 보관상의 어려움과 저장시 오염물 등 이물질이 묻기 쉽고, 시트가 잘 부서지며, 점착력이 약하여 제품을 제조시 첨가량을 늘리면 작업성이 급격히 떨어지는 문제점이 있었다.Among the above applications, the recycled resin used as a sheet is difficult to be packaged due to its large volume, and it is difficult to transport or store and contaminants such as contaminants during storage. Increasing the addition amount of the work had a problem of rapidly falling workability.

본 발명은 상기와 같은 문제점을 해결하기 위하여 안출된 것으로, 본 발명의 목적은 재생수지를 펠렛상으로 제조하여 부피를 획기적으로 줄일 수 있고, 운반이나 저장이 용이하여 이물질에 의한 오염을 방지할 수 있으며, 신소재 수지와 물성이 거의 동일하여 제품의 제조시 재생수지의 첨가량을 증가시킬 수 있는 경제성이 있는 재생수지를 제조하는 방법을 제공하는 것이다. The present invention has been made to solve the above problems, the object of the present invention is to produce a recycled resin in the form of pellets can significantly reduce the volume, can be easily transported or stored to prevent contamination by foreign matters In addition, the physical properties of the new material and the resin is almost the same to provide a method for producing a recycled resin with economical efficiency that can increase the amount of recycled resin added during manufacture of the product.

본 발명에 따른 재생수지 제조방법은Reclaimed resin manufacturing method according to the present invention

1) 발포상의 수지 스크랩을 분쇄하는 단계;1) milling the foamed resin scraps;

2) 분쇄된 수지 스크랩을 250~390℃의 온도로 1차 압출기에서 1차 해가교시키는 단계;2) first precrosslinking the pulverized resin scrap in a first extruder at a temperature of 250-390 ° C .;

3) 해가교된 용융물 100중량부에 대하여 신소재 수지 3~15중량부를 첨가하여 2차 압출기에서 펠렛화시키는 단계;3) pelletizing in a second extruder by adding 3 to 15 parts by weight of a new material resin based on 100 parts by weight of the crosslinked melt;

4) 펠렛을 냉각시키는 단계; 및4) cooling the pellets; And

5) 냉각된 펠렛을 절단하는 단계를 포함하는 것을 특징으로 한다.5) cutting the cooled pellets.

상기 단계 1)의 수지는 발포상인 것이면 어떠한 것이라도 무방하며, 에틸렌 비닐아세테이트 및/또는 폴리에틸렌 수지인 것이 바람직하다.The resin of step 1) may be any one as long as it is in a foamed state, and is preferably ethylene vinyl acetate and / or polyethylene resin.

상기 단계 1)은 수거된 수지 스크랩을 적절히 선별하여 1차 해가교시키기 전에 적절한 크기로 분쇄하는 단계로서, 분쇄기를 이용하여 약 20~45mm 크기로 분쇄하는 것이 바람직하다. 분쇄된 수지 스크랩은 다음의 단계 2)의 1차 압출기에 투입된다.Step 1) is a step of pulverizing the collected resin scraps to a suitable size before the first preliminary cross-linking, it is preferable to grind to about 20 ~ 45mm size using a grinder. The pulverized resin scrap is put into the first extruder of step 2) below.

상기 단계 2)는 단계 1)로부터 분쇄된 수지 스크랩을 고온에서 1차 해가교하는 단계로서, 1차 해가교 온도는 250~390℃이다. 상기 1차 해가교 온도는 수지 스크랩의 주요 성분의 열화를 방지하면서 해가교시키는 온도로서, 재생수지가 발포상으로 존재하기 때문에 신소재 수지의 열화 온도보다는 상당히 높은 온도인 특징이 있다. 상기 온도가 250℃ 미만인 경우에는 수지 스크랩이 완전히 해가교되지 않으며, 390℃를 초과하는 경우에는 재생수지를 사용한 제품 자체를 제조할 수 없다. 이러한 고온의 온도를 사용하여 해가교된 재생수지는, 단순히 열압착에 의하여 제조된 시트상의 재생수지보다 우수한 물성을 나타낼 수 있다.Step 2) is a step of primary crosslinking the resin scrap pulverized from step 1) at a high temperature, the first crosslinking temperature is 250 ~ 390 ℃. The primary crosslinking temperature is a temperature at which the crosslinking is performed while preventing the deterioration of the main components of the resin scrap, and is characterized in that the recycled resin is present in a foamed state, which is considerably higher than the degradation temperature of the new material resin. If the temperature is less than 250 ° C, the resin scrap is not completely crosslinked, and if it exceeds 390 ° C, the product itself using recycled resin cannot be manufactured. The reclaimed resin crosslinked using such a high temperature can exhibit physical properties superior to that of the sheet-shaped regenerated resin simply produced by thermocompression bonding.

1차 압출기를 통하여 해가교된 용융물은 1차 압출기의 배출구를 통하여 흘러나오는데, 이 과정에서, 자연 착화 현상이 발생하여 용융물에 존재하는 연소될 수 있는 이물질들이 완전 연소된다. 이러한 자연 착화 현상은 1차 압출기의 배출구가 250~390℃의 고온을 유지하기 때문인데, 용융물이 배출구로부터 흘러나올 때 스크랩 성분으로부터 자연적으로 가스 물질이 배출되어 착화가 시작되며, 이러한 가스 물질은 유기과산화물인 디쿠밀퍼옥사이드(dicumylperoxide, DCP) 잔여물과 발포제인 아조디카본아미드(azodicarbonamide, AC) 및 N,N-디니트로소 펜타메틸렌 테트라민(N,N-nirtoso pentamethylene tetramine) 잔여물이 섞여있는 경우 발생할 수 있다. 이와 같은 자연 착화 현상으로 수지 스크랩에 존재하는 이물질들 중 연소될 수 있는 것들이 완전히 제거되어 재생수지는 신소재 수지와 유사한 물성을 갖게 된다.The melt crosslinked through the primary extruder flows out through the outlet of the primary extruder. In this process, spontaneous ignition occurs and the combustible debris present in the melt is completely burned. This spontaneous ignition phenomenon is because the outlet of the primary extruder maintains a high temperature of 250 ~ 390 ℃, when the melt flows out of the outlet gas is naturally discharged from the scrap component to start the ignition, such a gas material is organic A mixture of peroxide dicumylperoxide (DCP) residue and blowing agent azodicarbonamide (AC) and N, N-dinitroso pentamethylene tetramine (N, N-nirtoso pentamethylene tetramine) residue May occur. Such spontaneous ignition phenomenon completely removes the combustibles among the foreign substances present in the resin scrap, so that the recycled resin has properties similar to those of the new material resin.

상기 단계 3)은 단계 2)로부터 나온 1차 해가교된 용융물에 신소재 수지를 혼합하여 2차 압출기를 통하여 펠렛화시키는 단계로서, 2차 압출기를 통하여 펠렛화되는 바람직한 과정은 다음과 같다:Step 3) is a step of mixing the new material resin in the primary crosslinked melt from step 2) and pelletizing it through a second extruder, the preferred process of pelletizing through a second extruder is as follows:

ⅰ) 1차 압출기를 통하여 나오는 1차 해가교된 용융물 100중량부에 대하여 신소재 수지 3~15중량부를 2차 압출기 투입구에 투입하고, 250~390℃의 온도에서 2차 해가교시키는 단계;Iii) 3-15 parts by weight of the new material resin is added to the second extruder inlet with respect to 100 parts by weight of the primary cross-linked melt coming out through the first extruder, and the second cross-linked at a temperature of 250-390 ° C .;

ⅱ) 상기 2차 해가교된 용융물을 2차 압출기 내의 1차 냉각장치에서 130~160℃의 온도로 냉각시키는 단계;Ii) cooling the secondary crosslinked melt to a temperature of 130 to 160 ° C. in a primary cooling device in a secondary extruder;

ⅲ) 상기 ⅱ) 단계에서 얻어진 용융물을 2차 압출기 내의 1차 가열장치에서 180~240℃의 온도로 가열시키는 단계;Iii) heating the melt obtained in step ii) at a temperature of 180-240 ° C. in a primary heating device in a secondary extruder;

ⅳ) 상기 ⅲ) 단계에서 얻어진 용융물을 2차 압출기 내의 2차 냉각장치에서 100~120℃의 온도로 냉각시키는 단계; 및Iii) cooling the melt obtained in step iii) to a temperature of 100-120 ° C. in a secondary cooling device in a secondary extruder; And

ⅴ) 상기 ⅳ) 단계에서 얻어진 용융물을 2차 압출기 내의 2차 가열장치에서 250~290℃의 온도로 최종가열하여 펠렛화시키는 단계.Iii) pelletizing the melt obtained in the above step iii) by heating it at a temperature of 250-290 ° C. in a secondary heating device in a secondary extruder.

상기 신소재 수지는 제조되는 제품의 용도에 따라서 적절한 것을 사용할 수 있으며, 바람직하게는 에틸렌 비닐아세테이트 및/또는 폴리에틸렌 수지이다. 상기 신소재 수지는 용융물 100중량부에 대하여 3~15중량부를 사용하는 것이 바람직하며, 3중량부 미만으로 첨가되는 경우에는 신소재 수지를 첨가하는 효과가 미미하며, 15중량부를 초과하는 경우에는 경제적이지 못한 문제점이 있다.The new material resin may be used according to the use of the product to be manufactured, preferably ethylene vinyl acetate and / or polyethylene resin. The new material resin is preferably used 3 to 15 parts by weight with respect to 100 parts by weight of the melt, when less than 3 parts by weight is added to the new material resin is insignificant, if more than 15 parts by weight is not economical There is a problem.

2차 압출기 내에서의 상기 과정의 다양한 온도들은 재생수지의 기본 물성이 변하지 않도록 하면서 펠렛상의 재생수지를 얻을 수 있는 바람직한 온도 범위로서, 상기 온도범위를 벗어나는 경우에는 제조된 재생수지의 물성이 저하되어 제품의 제조가 불가능해진다.The various temperatures of the process in the second extruder is a preferred temperature range for obtaining the pelletized recycled resin while keeping the basic physical properties of the recycled resin unchanged. The manufacture of the product becomes impossible.

상기 단계 3)의 i)단계에서는 단계 2)로부터의 용융물 및 신소재 수지와 함께 개질제로서의 오일을 더 첨가시킬 수 있다. 오일을 첨가하므로써 재생수지는 신소재 수지와 유사한 성능을 나타내게 된다. 상기 오일은 재생수지의 물성을 향상시킬 수 있는 것이면 공지된 어떠한 것이라도 무방하나, 바람직하게는 유동파라핀오일이다. 상기 오일은 용융물 100중량부에 대하여 3~10중량부로 첨가하는 것이 바람직한데, 3중량부 미만인 경우에는 오일 첨가 효과가 미미하고, 10중량부를 초과하는 경우에는 경제적으로 불리하다.In step i) of step 3), oil as a modifier may be further added together with the melt and the new material resin from step 2). By adding oil, the recycled resin will perform similarly to the new material resin. The oil may be any known one as long as it can improve the physical properties of the recycled resin, but is preferably a paraffin oil. Preferably, the oil is added in an amount of 3 to 10 parts by weight based on 100 parts by weight of the melt. If it is less than 3 parts by weight, the oil addition effect is insignificant, and when it exceeds 10 parts by weight, it is economically disadvantageous.

상기 2차 압출기의 주입구에는 1차 압출기로부터 나온 용융물 중 연소되지 않은 이물질을 걸러 줄 수 있는 망이 설치될 수 있으며, 이것에 의하여 2차 압출기로 도입되는 용융물에는 이물질이 전혀 포함되지 않게 된다. 또한, 2차 압출기의 배출구에는 원판(1)이 장착되며, 상기 원판에는 다수의 통공(2)이 존재하여 2차 압출기로부터 통공의 크기에 해당하는 직경을 갖는 펠렛화 된 재생수지가 생산된다.The injection port of the second extruder may be provided with a net for filtering the unburned foreign matter in the melt from the primary extruder, whereby the foreign material is not included in the melt introduced into the secondary extruder at all. In addition, the discharge port of the secondary extruder is equipped with a disc (1), the disc has a plurality of through holes (2) to produce a pelletized recycled resin having a diameter corresponding to the size of the through holes from the second extruder.

상기 단계 4)는 2차 압출기로부터 나온 긴 펠렛상의 재생수지를 냉각시키는 단계로서, 바람직하게는 펠렛상의 재생수지를 물에 침지시켜서 수행된다. 바람직한 물의 온도는 5~25℃이다. 냉각된 펠렛상의 재생수지는 단단하게 굳어지며, 다음의 절단 단계로 이어진다.Step 4) is a step of cooling the long pellet-like recycled resin from the secondary extruder, preferably by dipping the pellet-like recycled resin in water. Preferable water temperature is 5-25 degreeC. The recycled resin on the cooled pellets hardens and leads to the next cutting step.

상기 단계 5)는 냉각된 펠렛상의 재생수지를 포장 및 보관하기에 적당한 크기로 절단기를 사용하여 절단하는 과정으로서, 5~7mm 길이로 절단되는 것이 바람직하다. 이로서 과립형태의 재생수지의 제조가 완성되며, 완성된 재생수지는 포장과정을 거치게 된다.Step 5) is a process of cutting using a cutter to a size suitable for packaging and storing the cooled pellets on the cooled pellets, preferably cut to a length of 5 ~ 7mm. As a result, the production of granular recycled resin is completed, and the completed recycled resin goes through a packaging process.

상기 단계 1) 내지 단계 5)의 과정의 각 장치들은 순차적으로 연결되어 자동화된 공정으로 수행될 수 있다. 특히, 1차 압출기는 2기 이상을 사용할 수 있으며, 2기 이상의 1차 압출기의 각 배출구는 2차 압출기의 투입구에 함께 연결된다.Each device in the process of steps 1) to 5) may be sequentially connected and performed in an automated process. In particular, the primary extruder can use two or more, and each outlet of the two or more primary extruders is connected together to the inlet of the secondary extruder.

이하, 실시예를 통하여 본 발명의 더욱 상세하게 설명한다.Hereinafter, the present invention will be described in more detail with reference to Examples.

[[ 실시예Example ]]

1. One. 재생수지의Recycled resin 제조 Produce

에틸렌 비닐 아세테이트 및 폴리에틸렌을 주원료로 하는 수지 스크랩을 분쇄기로 평균 30mm 크기로 분쇄하고, 1차 압출기의 온도를 350℃로 하여 1차 해가교시켰다. The resin scrap containing ethylene vinyl acetate and polyethylene as a main raw material was crushed to an average size of 30 mm by a mill, and the first preliminary crosslinking was carried out at a temperature of 350 ° C for the first extruder.

1차 압출기를 통하여 나오는 1차 해가교된 용융물 100중량부에 대하여 신소 재 수지인 에틸렌 비닐 아세테이트 6중량부와 저밀도 폴리에틸렌 4중량부를 2차 압출기 투입구에 투입하고, 350℃의 온도에서 2차 해가교시키고, 2차 해가교된 용융물을 2차 압출기 내의 1차 냉각장치에서 150℃의 온도로 냉각시키고, 다음으로 2차 압출기 내의 1차 가열장치에서 200℃의 온도로 가열시키고, 2차 압출기 내의 2차 냉각장치에서 110℃의 온도로 냉각시키고, 마지막으로 2차 압출기 내의 2차 가열장치에서 260℃의 온도로 최종가열하여 펠렛화시켰다.6 parts by weight of ethylene vinyl acetate and 4 parts by weight of low-density polyethylene were added to the secondary extruder inlet with respect to 100 parts by weight of the primary crosslinked melt from the first extruder, and the second crosslinked at 350 ° C. And melt the secondary crosslinked melt to a temperature of 150 ° C. in the primary chiller in the secondary extruder, and then to a temperature of 200 ° C. in the primary heater in the secondary extruder, Cooled to a temperature of 110 ° C. in a secondary cooler and finally pelletized by final heating to a temperature of 260 ° C. in a secondary heater in a secondary extruder.

2차 압출기를 통하여 나오는 펠렛을 20℃의 물로 냉각시키고, 5mm 크기로 절단하여 재생수지를 제조하였다.The pellets coming out from the secondary extruder were cooled with water at 20 ° C. and cut into 5 mm sizes to prepare recycled resin.

재료(중량부)Material (part by weight) 재생수지Resin Resin 신소재 수지New material resin 에틸렌 비닐 아세테이트Ethylene vinyl acetate 66 6060 저밀도 폴리에틸렌Low density polyethylene 44 4040 재생수지Resin Resin 100100 --

2. 2. 재생수지Resin Resin 발포체의Foam 제조 Produce

상기 얻어진 재생수지와 신소재 수지 100중량부에 대하여 다음 표 2의 함량으로 각 성분들을 첨가하여 재생수지 발포체(실시예)와 신소재 수지 발포체(비교예)를 얻었다. Each component was added in the amounts shown in the following Table 2 with respect to the obtained resin and 100 parts by weight of the new material resin to obtain a recycled resin foam (Example) and a new material resin foam (Comparative Example).

성분(중량부)Ingredients (parts by weight) 실시예Example 비교예Comparative example CaCO3 CaCO 3 2020 2020 AC(azodicarbonamide)Azodicarbonamide 1010 1010 DCP(dicumylperoxide)DCP (dicumylperoxide) 1One 1One 스테아르산 Stearic acid 1.21.2 1.21.2 ZnOZnO 1.51.5 1.51.5 카본블랙Carbon black 0.50.5 0.50.5

3. 물성 측정3. Property measurement

상기 2에서 얻어진 재생수지 발포체(실시예)와 신소재 수지 발포체(비교예)로 에틸렌 비닐 아세테이트 스폰지를 제조하고, 물성을 측정하여 그 결과를 다음의 표 3에 나타내었다.Ethylene vinyl acetate sponge was prepared from the recycled resin foam (Example) and the new material resin foam (Comparative Example) obtained in the above 2, and the physical properties were measured, and the results are shown in Table 3 below.

시험항목 Test Items 단위 unit 결과result 시험방법 Test Methods 실시예Example 비교예Comparative example 강도(C-타입)Strength (C-Type) ScaleScale 26±126 ± 1 27±127 ± 1 KS M 6518KS M 6518 인장강도The tensile strength kg/cm3 kg / cm 3 99 1010 KS M 6518KS M 6518 신장율Elongation %% 143143 125125 KS M 6518KS M 6518 비중importance g/ccg / cc 0.060.06 0.060.06 KS M 6519KS M 6519 수축율Shrinkage %% 1.01.0 1.01.0 에이징 오븐 (aging oven) (70℃, 40분)Aging oven (70 ℃, 40 minutes)

상기 표 3에서 나타난 바와 같이, 신소재 수지와 재생수지를 혼합하여 사용한 실시예를 신소재 수지만을 사용한 비교예와 각 물성을 비교할 때, 강도, 인장강도, 비중 및 수축율에 있어서 거의 동일한 물성을 나타내었으며, 신장율에 있어서는 비교예보다 더욱 우수한 결과를 나타냈음을 알 수 있다.As shown in Table 3, when comparing the physical properties of the examples using the new material resin and the recycled resin with the comparative example using only the new material resin, the physical properties were almost the same in strength, tensile strength, specific gravity and shrinkage. In elongation rate, it turned out that the result was more excellent than the comparative example.

이상에서와 같이, 본 발명의 제조방법에 의하여 제조된 재생수지는 재생수지 자체의 포장 및 보관상의 우수성뿐만 아니라, 그 물성이 신소재 수지와 유사하여, 수지 제품에 다량으로 첨가되더라도 신소재 수지만을 사용한 제품과 동등한 정도의 물성을 나타내어 경제적인 효과가 우수하다.As described above, the recycled resin produced by the manufacturing method of the present invention, as well as the superiority of the packaging and storage of the recycled resin itself, its physical properties are similar to the new material resin, even if a large amount is added to the resin product product using only the new material resin It shows the same degree of physical properties as the economic effect is excellent.

Claims (6)

다음의 단계들을 포함하는 것을 특징으로 하는 재생수지 제조방법:Reclaimed resin manufacturing method comprising the following steps: 1) 에틸렌 비닐아세테이트 또는 폴리에틸렌 수지 스크랩을 분쇄하는 단계;1) grinding ethylene vinyl acetate or polyethylene resin scrap; 2) 분쇄된 수지 스크랩을 250~390℃의 온도로 1차 압출기에서 1차 해가교시키는 단계;2) first precrosslinking the pulverized resin scrap in a first extruder at a temperature of 250-390 ° C .; 3) 하기 i)~v)의 단계들을 통해 펠렛을 얻는 단계;3) obtaining pellet through the steps i) to v) below; ⅰ) 1차 압출기를 통하여 나오는 1차 해가교된 용융물 100중량부에 대하여 신소재 수지 3~15중량부를 2차 압출기 투입구에 투입하고, 250~390℃의 온도에서 2차 해가교시키는 단계,Iii) 3-15 parts by weight of the new material resin is added to the second extruder inlet with respect to 100 parts by weight of the primary crosslinked melt from the first extruder, and the second crosslinked at a temperature of 250 to 390 ° C., ⅱ) 상기 2차 해가교된 용융물을 2차 압출기 내의 1차 냉각장치에서 130~160℃의 온도로 냉각시키는 단계,Ii) cooling the secondary crosslinked melt to a temperature of 130 to 160 ° C. in a primary cooling device in a secondary extruder, ⅲ) 상기 ⅱ) 단계에서 얻어진 용융물을 2차 압출기 내의 1차 가열장치에서 180~240℃의 온도로 가열시키는 단계,Iii) heating the melt obtained in step ii) at a temperature of 180-240 ° C. in a primary heating device in a secondary extruder, ⅳ) 상기 ⅲ) 단계에서 얻어진 용융물을 2차 압출기 내의 2차 냉각장치에서 100~120℃의 온도로 냉각시키는 단계, 및Iii) cooling the melt obtained in step iii) at a temperature of 100-120 ° C. in a secondary cooling device in a secondary extruder, and ⅴ) 상기 ⅳ) 단계에서 얻어진 용융물을 2차 압출기 내의 2차 가열장치에서 250~290℃의 온도로 최종가열하여 펠렛화시키는 단계;Iii) pelletizing the melt obtained in step iii) by heating at a temperature of 250-290 ° C. in a secondary heating apparatus in a secondary extruder; 4) 펠렛을 냉각시키는 단계; 및4) cooling the pellets; And 5) 냉각된 펠렛을 절단하는 단계.5) cutting the cooled pellets. 삭제delete 삭제delete 제1항에 있어서, 단계 3)에서 신소재 수지는 에틸렌 비닐 아세테이트 및 폴리에틸렌 중 1종 이상인 것을 특징으로 하는 재생수지 제조방법.The method of claim 1, wherein the new material resin in step 3) is at least one of ethylene vinyl acetate and polyethylene. 제1항에 있어서, 단계 3)의 i)단계에서 오일을 더 첨가하는 것을 특징으로 하는 재생수지 제조방법.The method of claim 1, wherein the oil is further added in step i) of step 3). 제5항에 있어서, 상기 오일은 유동파라핀인 것을 특징으로 하는 재생수지 제조방법.6. The method of claim 5, wherein the oil is liquid paraffin.
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CN102363334A (en) * 2010-06-16 2012-02-29 金容培 Method and apparatus for manufacturing recycle scrap compound for car storage case pad
KR101697463B1 (en) 2016-08-09 2017-01-17 채경민 The method of manufacturing apparatus and manufacturing recycled resin using scraps
KR20200060124A (en) 2018-11-22 2020-05-29 (주)에스에스씨 Scrap regenerating device for plastic film production system
KR20200060123A (en) 2018-11-22 2020-05-29 (주)에스에스씨 Scrap processing device for plastic film production system

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KR102428808B1 (en) * 2022-02-23 2022-08-02 유정구 A method for manufacturing recycled resin using waste resin

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KR20020039364A (en) * 2000-08-09 2002-05-25 요시유키 칸다 Recycled polyester resin composition and molded articles thereof
JP2002292628A (en) 2001-03-28 2002-10-09 Sony Corp Method for reuse of used resin

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KR20020039364A (en) * 2000-08-09 2002-05-25 요시유키 칸다 Recycled polyester resin composition and molded articles thereof
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CN102363334A (en) * 2010-06-16 2012-02-29 金容培 Method and apparatus for manufacturing recycle scrap compound for car storage case pad
KR101697463B1 (en) 2016-08-09 2017-01-17 채경민 The method of manufacturing apparatus and manufacturing recycled resin using scraps
KR20200060124A (en) 2018-11-22 2020-05-29 (주)에스에스씨 Scrap regenerating device for plastic film production system
KR20200060123A (en) 2018-11-22 2020-05-29 (주)에스에스씨 Scrap processing device for plastic film production system

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