KR20020085079A - Making method of nontoxic resin compound and the nontoxic resin compound thereof - Google Patents

Making method of nontoxic resin compound and the nontoxic resin compound thereof Download PDF

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KR20020085079A
KR20020085079A KR1020010024348A KR20010024348A KR20020085079A KR 20020085079 A KR20020085079 A KR 20020085079A KR 1020010024348 A KR1020010024348 A KR 1020010024348A KR 20010024348 A KR20010024348 A KR 20010024348A KR 20020085079 A KR20020085079 A KR 20020085079A
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synthetic resin
resin compound
pvc
nontoxic
glycol
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KR1020010024348A
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Korean (ko)
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신병식
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주식회사 동남폴리머
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Publication of KR20020085079A publication Critical patent/KR20020085079A/en

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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
    • B29B9/12Making granules characterised by structure or composition
    • 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
    • C08J3/18Plasticising macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/04Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08L27/06Homopolymers or copolymers of vinyl chloride
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2027/00Use of polyvinylhalogenides or derivatives thereof as moulding material
    • B29K2027/06PVC, i.e. polyvinylchloride
    • 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
    • C08J2327/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
    • C08J2327/02Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
    • C08J2327/04Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08J2327/06Homopolymers or copolymers of vinyl chloride

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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)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE: A manufacturing method of nontoxic synthetic resin compound is provided to manufacture the nontoxic synthetic resin compound by mixing a principal raw material glycol based plasticizer and additives nontoxic stabilizer and pigment with PVC, a nontoxic synthetic resin compound manufactured by the method is provided. CONSTITUTION: In manufacturing a synthetic resin compound for preparing a raw material for manufacturing various children's toys medical instruments, various receptacles required in dietary life and industrial subsidiary materials, the manufacturing method of nontoxic synthetic resin compound comprises the processes of completely melting the blended materials by blending 100 kg of PVC (polyvinyl chloride) with 25 to 250 kg of glycol based plasticizer; and extrusion molding the blended materials into pellets using an extrusion molding machine at the temperature range of 178 to 182 deg.C, wherein a principal constituent of the manufactured nontoxic synthetic resin compound is 25 to 250 kg of glycol based plasticizer per 100 kg of PVC (polyvinyl chloride), and the glycol based plasticizer is citric acid based plasticizer.

Description

무 독성 합성수지 배합물의 제조방법과 이에 의해 제조한 합성수지 배합물{ MAKING METHOD OF NONTOXIC RESIN COMPOUND AND THE NONTOXIC RESIN COMPOUND THEREOF}Manufacturing method of non-toxic synthetic resin compound and synthetic resin compound produced thereby {MAKING METHOD OF NONTOXIC RESIN COMPOUND AND THE NONTOXIC RESIN COMPOUND THEREOF}

본 발명은 무 독성 합성수지 배합물의 제조방법과 이에 의해 제조한 합성수지 배합물에 관한 것으로 좀 더 상세하게는 각종 합성수지 완구, 지퍼용 슬립, 합성수지 파이프, 차량용 시트 내장재등을 제조하기 위해 사용하는 합성수지 배합물에서 유해물질에 해당되는 DBP(di-butyl phthalate), DIDP(di-isodecyl phthalate), DOA(di-octyl adipate), DOP(di-octyl phthalate) 및 DINP(di-isononyl phthalate)와 카드늄, 납의 검출이 없는 합성수지 배합물을 제공하기 위한 무 독성 합성수지 배합물의 제조방법과 이에 의해 제조한 합성수지 배합물에 관한 것이다.The present invention relates to a method for preparing a non-toxic synthetic resin compound and a synthetic resin compound prepared by the present invention. More specifically, the synthetic resin compound used to prepare various synthetic resin toys, zipper slips, synthetic resin pipes, vehicle seat interior materials, etc. Di-butyl phthalate (DBP), di-isodecyl phthalate (DIDP), di-octyl adipate (DOA), di-octyl phthalate (DOP) and di-isononyl phthalate (DINP), cadmium and lead A method for preparing a non-toxic synthetic resin formulation for providing a synthetic resin formulation and a synthetic resin formulation produced thereby.

일반적으로 합성수지 배합물은 플라스틱 완구로 통칭되는 합성수지 완구, 합성수지 지퍼용 슬립, 각종 합성수지 파이프, 식생활용 용기, 의료용구등을 제조하기 위한 기초 원료로 폭 넓게 사용되고 있다.In general, the synthetic resin compound is widely used as a base material for manufacturing synthetic resin toys, plastic zipper slip, synthetic resin pipes, food containers, medical equipment, etc., commonly referred to as plastic toys.

이때 합성수지 배합물은 주성분인 PVC(polyvinyl chloride)와 가소제(DOP)및 적량의 안정제를 배합하고, 필요에 따라 안료를 투여하여 1차적으로 제조한 합성수지 배합물(일명 compound라 칭하고 있음)을 이용하여 상기와 같은 각종 제품을 제조하고 있다.In this case, the synthetic resin compound is composed of a synthetic resin compound (hereinafter referred to as a compound) prepared primarily by combining PVC (polyvinyl chloride), a plasticizer (DOP), and an appropriate amount of stabilizer, and administering a pigment as necessary. Manufactures the same various products.

그런데 상기한 종래의 합성수지 배합물에서 인체에 유해한 여러 종의 물질이 검출되어 그 사용이 제한되어 오고 있는 실정이다.However, in the conventional synthetic resin formulations, various substances harmful to the human body have been detected and their use has been limited.

그중에서도 특히 인체의 내분비계 장애 물질로 알려져 있는 DBP(di-butyl phthalate), DIDP(di-isodecyl phthalate), DOA(di-octyl adipate), DOP(di-octyl phthalate) 및 DINP(di-isononyl phthalate)와 중금속에 해당되어 각종 질병을 유발케하는 카드늄, 납등의 검출이 큰 문제로 대두하고 있다.Among them, di-butyl phthalate (DBP), di-isodecyl phthalate (DIDP), di-octyl adipate (DOA), di-octyl phthalate (DOP), and di-isononyl phthalate (DINP), among others, are known as endocrine disruptors. And heavy metals, which cause various diseases, such as the detection of cadmium, lead is emerging as a big problem.

따라서 합성수지 배합물을 제조하는 업계에서는 위에서와 같은 유해 물질인 환경호르몬이 검출되지 않는 합성수지 배합물의 제공이 절실한 입장이다.Therefore, in the industry of manufacturing a synthetic resin formulation, it is urgent to provide a synthetic resin formulation in which environmental hormones, which are harmful substances as described above, are not detected.

본 발명은 이러한 종래의 문제점을 감안하여 상기한 바와 같은 DBP(di-butyl phthalate), DIDP(di-isodecyl phthalate),DOA(di-octyl adipate), DOP(di-octyl phthalate), DINP(di-isononyl phthalate), 카드늄, 납과 같은 독성을 가진 환경호르몬 물질의 검출이 없는 합성수지 배합물을 제공하고자 이미 사용되고 있는 여러 종류의 화학물질을 사용하여 본래의 목적인 최종 제품의 성형성, 형태성, 견고성등을 고려하면서도 위와 같은 독성 물질에 해당하는 환경호르몬 물질이 검출되지 않는 합성수지 배합물을 제공하고자 각고의 노력으로 본 발명을 완성할 수 있었다.In view of the above problems, the present invention provides the above-mentioned di-butyl phthalate (DBP), di-isodecyl phthalate (DIDP), di-octyl adipate (DOA), di-octyl phthalate (DOP), and DIN- (di-). In order to provide synthetic resin formulations without detection of toxic environmental hormone substances such as isononyl phthalate), cadmium, and lead, various types of chemicals already used are used to improve the formability, formability and firmness of the final product. While considering, the present invention could be completed by efforts to provide a synthetic resin formulation in which environmental hormone substances corresponding to the above toxic substances are not detected.

본 발명에서는 주 원료가 되는 PVC(polyvinyl chloride)에 클리콜(glycol)계가소제를 주원료로 배합하고, 종래부터 사용된 무독 안정제, 안료등을 적량 배합하여 제조한 합성수지 배합물을 제공함으로서 본 발명의 목적을 달성할 수 있었다.In the present invention, a synthetic resin formulation prepared by blending a glycol plasticizer as a main raw material to PVC (polyvinyl chloride), which is a main raw material, and a suitable amount of a conventionally used non-toxic stabilizer, pigment, etc. is provided. Could achieve.

그러나 최종 완제품을 제조하기 위한 성형성, 형태성등을 고려하여야 하므로 상기한 클리콜(glycol)계 가소제의 사용을 제한함으로서 가능하였다.However, it is possible to limit the use of the above-mentioned glycol plasticizers, because the moldability, formability, etc. for the final finished product should be considered.

이하 본 발명을 구체적으로 살펴 보면 다음과 같다.Looking in more detail below the present invention.

PVC(polyvinyl chloride) 100㎏을 기준으로 정량한 상태에서 클리콜(glycol)계 가소제 25 ∼250㎏을 정량하여 서로 충분히 배합하여 가열상태에서 압출 성형하여 합성수지 배합물을 제공하는데 특징이 있다.In the state quantified based on 100kg of PVC (polyvinyl chloride), it is characterized by providing a synthetic resin compound by quantitating 25 to 250kg of a plasticizer plasticizer sufficiently mixed with each other and extruding in a heated state.

이때 상기한 PVC(polyvinyl chloride)와 클리콜(glycol)계 가소제를 배합할때 종래와 같이 배합물의 균일한 배합과 가열 성형시 소성등을 방지하게 위해 사용하는 안정제 및 색상을 나타내기 위해 사용하는 안료는 선택적으로 사용이 가능하나 이는 필요에 따라 극소량을 사용하는 것이므로 본 발명에서 제공하고자 하는 합성수지 배합물의 특성에 크게 영향을 미치지 아니한다.At this time, when blending the above-mentioned PVC (polyvinyl chloride) and glycol-based plasticizers, pigments used to express the stabilizer and color used to prevent the uniform mixing of the blend and plasticity during heat molding as in the prior art May be optionally used, but this is to use a very small amount as necessary, so does not significantly affect the properties of the synthetic resin formulation to be provided in the present invention.

또한 필요에 따라 무독성 안정제를 투입하여 배합하여 사용할 수도 있으나, 무독성 안정제의 경우에는 통상적으로 사용되어온 ESO(epoxidized soybean oil)의 사용에 비하여 신체적 영향을 미치지 않는다는 것을 제외하고는 일반적으로 사용되어온 안정제와 동일한 역할을 한다.In addition, a non-toxic stabilizer may be added and used as necessary, but the non-toxic stabilizer is the same as a stabilizer generally used except that it does not have a physical effect compared to the use of an epoxidized soybean oil (ESO). Play a role.

이러한 본 발명에 있어서, 상기한 PVC(polyvinyl chloride) 100㎏을 기준으로 정량한 상태에서 클리콜(glycol)계 가소제 25㎏이하로 조성하는 경우에는PVC(polyvinyl chloride)가 완전한 용해에 해당하는 배합에 오랜 시간이 요구될 뿐만 아니라 용해하여 가열 상태에서 쉽게 딱딱해져서 압출이 이루어지지 않은 문제점이 있다.In the present invention, when the composition is quantified on the basis of 100kg of PVC (polyvinyl chloride) below 25kg of glycol plasticizers, the composition of PVC (polyvinyl chloride) corresponds to the complete dissolution. Not only does it require a long time, there is a problem that the extrusion is hardened easily in a heated state, so that extrusion is not performed.

그리고 상기한 PVC(polyvinyl chloride) 100㎏을 기준으로 정량한 상태에서 클리콜(glycol)계 가소제 250㎏이상으로 조성하는 경우에는 PVC(polyvinyl chloride)가 짧은 시간안에 완전히 용해되는 장점은 있으나 가열 상태에서 압출하여도 반죽상태를 유지하면서 압출되지 아니하고 그대로 액상화된 상태로 그대로 유지되어 전혀 성형성이 없는 단점이 있었다.In addition, when the composition is quantified based on 100 kg of PVC (polyvinyl chloride), the composition is more than 250 kg of a glycol plasticizer, but PVC (polyvinyl chloride) is completely dissolved in a short time. Even when extruded, it was not extruded while maintaining the kneading state, but was kept in a liquefied state as it was, so there was no drawability at all.

따라서 합성수지 배합물의 상태로 제조하여 운반, 저장 및 생산 상태를 감안할 때 PVC(polyvinyl chloride) 100㎏당 클리콜(glycol)계 가소제 25∼250㎏으로 정량하여 배합하는 것이 가장 적당하였다.Therefore, in consideration of the transport, storage and production conditions of the synthetic resin formulation, it was most suitable to quantify and mix 25-250 kg of glycol-based plasticizer per 100 kg of PVC (polyvinyl chloride).

이러한 본 발명에 의하여 제조된 합성수지 배합물은 상기한 바와 같이 서로 충분한 배합에 의하여 완전 용해시킨 다음, 가열 상태에서 압출 성형되면서 배출되는 배합물을 절단하여 페릿화하여 저장하였다가 완구 또는 각종 합성수지 제품으로 성형 제조하여 사용하면 된다.The synthetic resin formulations prepared according to the present invention are completely dissolved by mutually sufficient mixing as described above, and then cut and stored in a pelletized formulation which is discharged while being extruded in a heated state and manufactured into a toy or various synthetic resin products. Can be used.

이러한 본 발명에 의하여 제조된 합성수지 배합물에서는 DBP(di-butyl phthalate), DIDP(di-isodecyl phthalate),DOA(di-octyl adipate), DOP(di-octyl phthalate), DINP(di-isononyl phthalate), 카드늄, 납, 수은과 같은 독성을 가진 환경호르몬 물질의 검출이 없었는데 그 구체적인 사례에 대하여 본 발명을 구체적으로 실시한 실시예와 시험예에 의하여 본 발명을 살펴보기로 한다.In the synthetic resin formulation prepared according to the present invention, di-butyl phthalate (DBP), di-isodecyl phthalate (DIDP), di-octyl adipate (DOA), di-octyl phthalate (DOP), di-isononyl phthalate (DINP), There was no detection of toxic environmental hormone substances such as cadmium, lead, mercury, and the present invention will be described by examples and test examples in which the present invention is specifically performed.

실시예 1Example 1

PVC(polyvinyl chloride)로 상품명 LS-100수지(주식회사 엘지화학) 50㎏을 정량하고, 클리콜(glycol)계 가소제로 EBN 330(alkyl aryl ester of glycol; 주식회사 엘지화학) 10㎏을 정량하고, 무독 안정제로 CZ-122(Witco사 독일) 2㎏, E.S.O 안정제(경서산업주식회사) 1㎏, 안료로 MDAC 및 군청안료(효진안료) 10g으로 각각 정량하여 배합기에 투여하여 교반을 시작하였다.50 kg of LS-100 resin (LG Chemical Co., Ltd.) was weighed with polyvinyl chloride (PVC), and 10 kg of EBN 330 (alkyl aryl ester of glycol; LG Chem Co., Ltd.) was weighed with a glycol-based plasticizer. 2 kg of CZ-122 (Witco, Germany) as a stabilizer, 1 kg of ESO stabilizer (Gyeongseo Industrial Co., Ltd.), and 10 g of MDAC and Guncheong Pigment (Hyojin Pigment) were used as pigments.

완전한 용해가 이루어지는 시간이 지나면 지날수록 용해 속도가 늦어지고, 강제로 교반을 행하여 용해가 이루어지는 시간이 약 50여분 소요되었으며, 특히 그 굳기가 너무 딱딱하였다.As time passed for complete dissolution, the dissolution rate was slowed down, and it took about 50 minutes for the dissolution to occur by forcible stirring, in particular, the hardness thereof was too hard.

이러한 용해후 가열 온도범위 178∼182℃를 유지하는 압출기에 강제로 투여하는 방법에 의하여 압출을 행하여 압출물이 배출되기 시작하였는데 초기의 압출물의 굳기가 너무 강하여 중간에 압출물이 끊어지는 현상이 두드러졌고, 열에 의해 부분적으로 소성된 배합물이 배출되기 시작하면서 압출기에 부하가 걸리기 시작하여 압출 작업이 불가능하였다.After dissolving, the extrudate began to be discharged by a method of forcibly administered to an extruder maintaining a heating temperature range of 178 to 182 ° C. The initial extrudates were so hard that the extrudate was severely interrupted. And the extruder was unable to load due to the extruder being loaded as the partially calcined blend began to exit with heat.

실시예 2Example 2

PVC(polyvinyl chloride)로 상품명 LS-100수지(주식회사 엘지화학) 50㎏을 정량하고, 클리콜(glycol)계 가소제로 EBN 330(alkyl aryl ester of glycol; 주식회사 엘지화학) 130㎏을 정량하고, 무독 안정제로 CZ-122(Witco사 독일) 2㎏, E.S.O 안정제(경서산업주식회사) 1㎏, 안료로 MDAC 및 군청안료(효진안료) 10g으로각각 정량하여 배합기에 투여하여 교반을 시작하였다.50 kg of LS-100 resin (LG Chemical Co., Ltd.) was weighed with polyvinyl chloride (PVC), 130 kg of EBN 330 (alkyl aryl ester of glycol; LG Chem Co., Ltd.) was weighed with a glycol-based plasticizer. As a stabilizer, 2 kg of CZ-122 (Witco, Germany), 1 kg of ESO stabilizer (Gyeongseo Industrial Co., Ltd.), and 10 g of MDAC and Guncheong Pigment (Hyojin Pigment) were used as pigments.

약 2분이 지나자 완전한 용해가 이루어졌고, 이러한 상태에서 압출기에 투여하여 압출을 시작하였다.After about 2 minutes complete dissolution had occurred, and in this state, extrusion was started by administration to an extruder.

이때 압출기의 가열 온도범위는 178∼182℃로 유지하였다.At this time, the heating temperature range of the extruder was maintained at 178 ~ 182 ℃.

압출기에 투입후 즉시 압출물이 배출되기 시작하였는데 그 압출물은 완전한 액상상태를 유지한 상태로 배출되어 페릿화할 수 없었다.The extrudate began to be discharged immediately after being fed into the extruder, and the extrudate was discharged in a completely liquid state and could not be pelletized.

실시예 3Example 3

PVC(polyvinyl chloride)로 상품명 LS-100수지(주식회사 엘지화학) 50㎏을 정량하고, 클리콜(glycol)계 가소제로 EBN 330(alkyl aryl ester of glycol; 주식회사 엘지화학) 100㎏을 정량하고, 무독 안정제로 CZ-122(Witco사 독일) 2㎏, E.S.O 안정제(경서산업주식회사) 1㎏, 안료로 MDAC 및 군청안료(효진안료) 10g으로 각각 정량하여 배합기에 투여하여 교반을 시작하였다.50 kg of LS-100 resin (LG Chemical Co., Ltd.) was weighed with polyvinyl chloride (PVC) and 100 kg of EBN 330 (alkyl aryl ester of glycol; LG Chem Co., Ltd.) was weighed with a glycol-based plasticizer. 2 kg of CZ-122 (Witco, Germany) as a stabilizer, 1 kg of ESO stabilizer (Gyeongseo Industrial Co., Ltd.), and 10 g of MDAC and Guncheong Pigment (Hyojin Pigment) were used as pigments.

완전한 용해가 이루어지는 시간이 약 3 여분 소요되었다.The complete dissolution took about 3 extra hours.

이러한 용해후 가열 온도범위 178∼182℃를 유지하는 압출기에 강제로 투여하는 방법에 의하여 압출을 행하였더니 배출되는 압출물의 굳기가 약하여 압출물이 부분적으로 흘러내리면서 끊어지는 현상은 발생하였으나 절단기에 의해 펠릿화하는 데에는 크게 문제가 되지 않았다.After the dissolution, extrusion was carried out by a method of forcibly administered to an extruder maintaining a heating temperature range of 178 to 182 ° C., and the extrudate was partially broken down due to the hardening of the discharged extrudate. Pelletizing was not a big problem.

실시예 4Example 4

PVC(polyvinyl chloride)로 상품명 LS-100수지(주식회사 엘지화학) 50㎏을 정량하고, 클리콜(glycol)계 가소제로 EBN 330(alkyl aryl ester of glycol; 주식회사 엘지화학) 50㎏을 정량하고, 무독 안정제로 CZ-122(Witco사 독일) 2㎏, E.S.O 안정제(경서산업주식회사) 1㎏, 안료로 MDAC 및 군청안료(효진안료) 10g으로 각각 정량하여 배합기에 투여하여 교반을 시작하였다.50 kg of LS-100 resin (LG Chemical Co., Ltd.) was weighed with polyvinyl chloride (PVC), and 50 kg of EBN 330 (alkyl aryl ester of glycol; LG Chem Co., Ltd.) was weighed with a glycol-based plasticizer. 2 kg of CZ-122 (Witco, Germany) as a stabilizer, 1 kg of ESO stabilizer (Gyeongseo Industrial Co., Ltd.), and 10 g of MDAC and Guncheong Pigment (Hyojin Pigment) were used as pigments.

완전한 용해가 이루어지는 시간이 약 4여분 소요되었다.The complete dissolution took about 4 minutes.

이러한 용해후 가열 온도범위 178∼182℃를 유지하는 압출기에 강제로 투여하는 방법에 의하여 압출을 행하였더니 배출되는 압출물의 굳기가 상기한 실시예 3보다 강하였고, 또한 압출물이 흘러내리지는 않았으나 부분적으로 늘어지는 현상이 발생하였다.Extrusion was performed by the method of forcibly administering to an extruder maintaining a heating temperature range of 178 to 182 ° C after dissolution. The extrudates of the discharged extrudates were stronger than those of Example 3, and the extrudate did not flow down, but partially. The phenomenon of sagging occurred.

그러나 절단기에 의해 펠릿화하는 데에는 크게 문제가 되지 않았다.However, it was not a big problem for pelletizing by a cutter.

실시예 5Example 5

PVC(polyvinyl chloride)로 상품명 LS-100수지(주식회사 엘지화학) 50㎏을 정량하고, 클리콜(glycol)계 가소제로 EBN 330(alkyl aryl ester of glycol; 주식회사 엘지화학) 25㎏을 정량하고, 무독 안정제로 CZ-122(Witco사 독일) 2㎏, E.S.O 안정제(경서산업주식회사) 1㎏, 안료로 MDAC 및 군청안료(효진안료) 10g으로 각각 정량하여 배합기에 투여하여 교반을 시작하였다.50 kg of LS-100 resin (LG Chemical Co., Ltd.) was weighed with polyvinyl chloride (PVC), and 25 kg of EBN 330 (alkyl aryl ester of glycol; LG Chem Co., Ltd.) was weighed with a glycol-based plasticizer. 2 kg of CZ-122 (Witco, Germany) as a stabilizer, 1 kg of ESO stabilizer (Gyeongseo Industrial Co., Ltd.), and 10 g of MDAC and Guncheong Pigment (Hyojin Pigment) were used as pigments.

완전한 용해가 이루어지는 시간이 약 4여분 소요되었다.The complete dissolution took about 4 minutes.

이러한 용해후 가열 온도범위 178∼182℃를 유지하는 압출기에 강제로 투여하는 방법에 의하여 압출을 행하였더니 배출되는 압출물의 굳기가 마치 밀가루를 반죽한 상태로 유지되면서 이상적으로 배출되었고, 절단기에 의하여 절단 작업이 매우 용이하여 펠릿화하는데 매우 이상적인 작업이 가능하였다.After the dissolution, the extrusion was performed by a method of forcibly administered to an extruder maintaining a heating temperature range of 178 to 182 ° C., and the solidified product of the discharged product was discharged ideally while maintaining the state of kneading flour, and was cut by a cutter. The work was so easy that the ideal work for pelletization was possible.

시험예 1Test Example 1

상기 실시예 3에서 제조한 압출물 3㎏을 시료로 채택하여 식품의약품안전청 고시 2000-60호에 의거하여 DBP(di-butyl phthalate), DIDP(di-isodecyl phthalate), DOA(di-octyl adipate), DOP(di-octyl phthalate) 및 DINP(di-isononyl phthalate)와 같은 환경호르몬 물질의 검출의 여부를 확인하여 보았다.3 kg of the extrudate prepared in Example 3 was used as a sample, and according to Korean Food and Drug Administration Notice 2000-60, DBP (di-butyl phthalate), DIDP (di-isodecyl phthalate), and DOA (di-octyl adipate) , The detection of environmental hormone substances such as di-octyl phthalate (DOP) and di-isononyl phthalate (DINP).

식품의약품안정청에서는 상기한 DBP(di-butyl phthalate), DIDP(di-isodecyl phthalate), DOA(di-octyl adipate), DOP(di-octyl phthalate) 및 DINP(di-isononyl phthalate)의 검출 한계를 1㎏당 50㎎의 허용하고 있으나 상기한 실시예 3의 압출물에서는 상기한 유해물질인 환경호르몬 물질이 전혀 검출되지 않았다.The Food and Drug Administration limits the detection limits of the above-mentioned di-butyl phthalate (DBP), di-isodecyl phthalate (DIDP), di-octyl adipate (DOA), di-octyl phthalate (DOP), and di-isononyl phthalate (DINP). Although 50 mg / kg is allowed, the above-described extrudates of Example 3 did not detect any of the above-mentioned environmental hormone substances.

시험예 2Test Example 2

상기 실시예 4에서 제조한 압출물 3㎏을 시료로 채택하여 식품의약품안전청 고시 2000-60호에 의거하여 DBP(di-butyl phthalate), DIDP(di-isodecyl phthalate), DOA(di-octyl adipate), DOP(di-octyl phthalate) 및 DINP(di-isononyl phthalate)와 같은 환경호르몬 물질의 검출의 여부를 확인하여 보았다.3 kg of the extrudate prepared in Example 4 was used as a sample, and according to Korean Food and Drug Administration Notice 2000-60, DBP (di-butyl phthalate), DIDP (di-isodecyl phthalate), and DOA (di-octyl adipate) , The detection of environmental hormone substances such as di-octyl phthalate (DOP) and di-isononyl phthalate (DINP).

식품의약품안정청에서는 상기한 DBP(di-butyl phthalate), DIDP(di-isodecylphthalate), DOA(di-octyl adipate), DOP(di-octyl phthalate) 및 DINP(di-isononyl phthalate)의 검출 한계를 1㎏당 50㎎의 허용하고 있으나 상기한 실시예 3의 압출물에서는 상기한 유해물질인 환경호르몬 물질이 전혀 검출되지 않았다.The Korea Food and Drug Administration sets a limit of detection of the above-mentioned detection limits for 50 mg of sugar was allowed, but the environmental hormone substance, which was the above-mentioned harmful substance, was not detected at all in the extrudate of Example 3.

시험예 3Test Example 3

상기 실시예 5에서 제조한 압출물 3㎏을 시료로 채택하여 식품의약품안전청 고시 2000-60호에 의거하여 DBP(di-butyl phthalate), DIDP(di-isodecyl phthalate), DOA(di-octyl adipate), DOP(di-octyl phthalate) 및 DINP(di-isononyl phthalate)와 같은 환경호르몬 물질의 검출의 여부를 확인하여 보았다.3 kg of the extrudate prepared in Example 5 was used as a sample, and according to Korean Food and Drug Administration Notice 2000-60, DBP (di-butyl phthalate), DIDP (di-isodecyl phthalate), and DOA (di-octyl adipate) , The detection of environmental hormone substances such as di-octyl phthalate (DOP) and di-isononyl phthalate (DINP).

식품의약품안정청에서는 상기한 DBP(di-butyl phthalate), DIDP(di-isodecyl phthalate), DOA(di-octyl adipate), DOP(di-octyl phthalate) 및 DINP(di-isononyl phthalate)의 검출 한계를 1㎏당 50㎎의 허용하고 있으나 상기한 실시예 3의 압출물에서는 상기한 유해물질인 환경호르몬 물질이 전혀 검출되지 않았다.The Food and Drug Administration limits the detection limits of the above-mentioned di-butyl phthalate (DBP), di-isodecyl phthalate (DIDP), di-octyl adipate (DOA), di-octyl phthalate (DOP), and di-isononyl phthalate (DINP). Although 50 mg / kg is allowed, the above-described extrudates of Example 3 did not detect any of the above-mentioned environmental hormone substances.

시험예 4Test Example 4

상기 실시예 3에서 제조한 압출물 3㎏을 시료로 채택하여 ICP 분석 시험방법에 의거하여 납(Pb)과 카드늄(Cd)의 검출의 여부를 확인하여 보았다.3 kg of the extrudate prepared in Example 3 was used as a sample, and the detection of lead (Pb) and cadmium (Cd) was confirmed based on the ICP analysis test method.

검출 단위는 wt/ppm이였으며, 상기한 실시예 3에서 제조한 압출물에서는 납과 카드늄이 전혀 검출되지 않았다.The detection unit was wt / ppm, and lead and cadmium were not detected at all in the extrudate prepared in Example 3.

시험예 5Test Example 5

상기 실시예 4에서 제조한 압출물 3㎏을 시료로 채택하여 ICP 분석 시험방법에 의거하여 납(Pb)과 카드늄(Cd)의 검출의 여부를 확인하여 보았다.3 kg of the extrudate prepared in Example 4 was used as a sample, and the detection of lead (Pb) and cadmium (Cd) was confirmed based on the ICP analysis test method.

검출 단위는 wt/ppm이였으며, 상기한 실시예 4에서 제조한 압출물에서는 납과 카드늄이 전혀 검출되지 않았다.The detection unit was wt / ppm, and lead and cadmium were not detected at all in the extrudate prepared in Example 4.

시험예 6Test Example 6

상기 실시예 5에서 제조한 압출물 3㎏을 시료로 채택하여 ICP 분석 시험방법에 의거하여 납(Pb)과 카드늄(Cd)의 검출의 여부를 확인하여 보았다.3 kg of the extrudate prepared in Example 5 was used as a sample, and the detection of lead (Pb) and cadmium (Cd) was confirmed based on the ICP analysis test method.

검출 단위는 wt/ppm이였으며, 상기한 실시예 5에서 제조한 압출물에서는 납과 카드늄이 전혀 검출되지 않았다.The detection unit was wt / ppm, and lead and cadmium were not detected at all in the extrudate prepared in Example 5.

이상 상기의 시험예 1, 2, 3, 4, 5, 6,에서 살펴 본 바와 같이 본 발명에 의하여 제조된 합성수지 배합물은 유해물질로서 각종 질환을 유발케하는 상기한 환경호르몬 물질이 검출되지 않았으며, 특히 본 발명에서는 상기한 클리콜(glycol)계 가소제대신에 구연산계 가소제를 사용하여도 상기한 유해물질이 생산물에서 검출이 없을 것으로 판단하고 있으며, 상기한 구연산계 가소제는 acetyl tri-butyl citrate의 사용이다.As described above in Test Examples 1, 2, 3, 4, 5, 6, the synthetic resin formulation prepared according to the present invention was not detected as the environmental hormone substances causing the various diseases as harmful substances. In particular, in the present invention, even when citric acid plasticizers are used instead of the above-mentioned glycol plasticizers, it is determined that the above-mentioned harmful substances are not detected in the product, and the citric acid plasticizers of acetyl tri-butyl citrate Use.

결국, 본 발명에서는 글리콜계 가소제의 한정 사용으로 인하여 상기한 유해물질이 검출되지 않는 합성수지 배합물을 제공할 수 있었고, 또한 글리콜계 가소제대신에 구연산계 가소제의 사용을 사용하여도 구체적인 독성물질이 검출되지 않을 것으로 확신한다.As a result, the present invention could provide a synthetic resin formulation in which the above hazardous substances were not detected due to the limited use of the glycol plasticizer, and no specific toxic substances were detected even when the citric acid plasticizer was used instead of the glycol plasticizer. I'm sure it won't.

따라서 글리콜계 가소제 또는 이에 준하는 구연산계 가소제를 사용하여도 상기한 바와 같은 유해 물질의 검출이 없다면 본 발명의 권리범위에 속하는 것임을 밝혀둔다.Therefore, even if a glycol-based plasticizer or a citric acid-based plasticizer is used, if the detection of the harmful substances as described above is found to be within the scope of the present invention.

이상 상기에서 상세히 살핀 바와 같이 본 발명의 방법에 의하여 제조된 합성수지 배합물은 내분비계 장애가 우려되는 유해물질인 환경호르몬 물질 및 카드늄, 납과 같은 중금속이 검출되지 않으므로 해서 각종 어린이용 완구, 의료용구, 각종 생활에 필요한 용기, 산업용 부자재등을 제조하여도 인체에 해가 없으므로 안전하게 할 수 있는 매우 유용한 발명임이 분명하다.As described in detail above, the synthetic resin formulation prepared by the method of the present invention is a harmful substance for which endocrine disorders are concerned, and heavy metals such as cadmium and lead are not detected. It is obvious that it is a very useful invention that can be safely made because there is no harm to the human body even if a container, industrial auxiliary material, etc. necessary for living is manufactured.

Claims (3)

각종 어린이용 완구, 의료용구, 각종 식생활에 필요한 용기, 산업용 부자재등을 제조하기 위한 원료의 전 단계로 사용하는 합성수지 배합물을 제조함에 있어서,In the manufacture of synthetic resin formulations used in all stages of raw materials for the production of various children's toys, medical equipment, containers for various dietary life, industrial auxiliary materials, PVC(polyvinyl chloride) 100㎏ 당 글리콜(glycol)계 가소제 25 ∼250㎏로 정량하여 배합하는 것에 의해 완전히 용해 한 후, 종래와 동일한 온도로 가열상태에서 압출 성형하여 펠릿화하는 것을 특징으로 하는 무독성 합성수지 배합물의 제조방법.Non-toxic synthetic resin, characterized in that it is completely dissolved by quantitatively blending with 25 to 250 kg of glycol-based plasticizer per 100 kg of PVC (polyvinyl chloride), and then extruding by heating at the same temperature as before. Method of Preparation of Formulations. 청구항 1에 의하여 제조된 무독성 합성수지 배합물의 주성분이 PVC(polyvinyl chloride) 100㎏ 당 글리콜(glycol)계 가소제 25 ∼250㎏인 것을 특징으로 하는 무독성 합성수지 배합물.Non-toxic synthetic resin compound prepared according to claim 1 is a non-toxic synthetic resin compound, characterized in that the main component of the glycol plasticizer 25 to 250 kg per 100 kg PVC (polyvinyl chloride). 청구항 2에 있어서,The method according to claim 2, 상기한 글리콜(glycol)계 가소제가 구연산계 가소제인 것을 특징으로 하는 무독성 합성수지 배합물.Non-toxic synthetic resin compound, characterized in that the glycol plasticizer is a citric acid plasticizer.
KR1020010024348A 2001-05-04 2001-05-04 Making method of nontoxic resin compound and the nontoxic resin compound thereof KR20020085079A (en)

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01113450A (en) * 1987-10-27 1989-05-02 Chisso Corp Vinyl chloride resin composition
JPH02269145A (en) * 1989-03-14 1990-11-02 Okamoto Ind Inc Vinyl chloride-based resin composition for packaging food
JPH041251A (en) * 1990-04-19 1992-01-06 Furukawa Electric Co Ltd:The Temperature-sensitive polymer material
US5344864A (en) * 1988-07-15 1994-09-06 Denki Kagaku Kogyo Kabushiki Kaisha Polyvinyl chloride thermoplastic elastomer composition
KR970705601A (en) * 1996-02-16 1997-10-09 마츠다 겐지로 ANTI-BACTERIAL FILM SUITABLE FOR FOOD PACKAGING

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01113450A (en) * 1987-10-27 1989-05-02 Chisso Corp Vinyl chloride resin composition
US5344864A (en) * 1988-07-15 1994-09-06 Denki Kagaku Kogyo Kabushiki Kaisha Polyvinyl chloride thermoplastic elastomer composition
JPH02269145A (en) * 1989-03-14 1990-11-02 Okamoto Ind Inc Vinyl chloride-based resin composition for packaging food
JPH041251A (en) * 1990-04-19 1992-01-06 Furukawa Electric Co Ltd:The Temperature-sensitive polymer material
KR970705601A (en) * 1996-02-16 1997-10-09 마츠다 겐지로 ANTI-BACTERIAL FILM SUITABLE FOR FOOD PACKAGING

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