KR102191338B1 - Eco-friendly composition improved in biodegradability and plasticity and the preparation method thereof - Google Patents

Eco-friendly composition improved in biodegradability and plasticity and the preparation method thereof Download PDF

Info

Publication number
KR102191338B1
KR102191338B1 KR1020190119231A KR20190119231A KR102191338B1 KR 102191338 B1 KR102191338 B1 KR 102191338B1 KR 1020190119231 A KR1020190119231 A KR 1020190119231A KR 20190119231 A KR20190119231 A KR 20190119231A KR 102191338 B1 KR102191338 B1 KR 102191338B1
Authority
KR
South Korea
Prior art keywords
starch
composition
weight
parts
present
Prior art date
Application number
KR1020190119231A
Other languages
Korean (ko)
Inventor
이만기
이석원
이민주
Original Assignee
(주)길마로
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 (주)길마로 filed Critical (주)길마로
Priority to KR1020190119231A priority Critical patent/KR102191338B1/en
Application granted granted Critical
Publication of KR102191338B1 publication Critical patent/KR102191338B1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L3/00Compositions of starch, amylose or amylopectin or of their derivatives or degradation products
    • C08L3/04Starch derivatives, e.g. crosslinked derivatives
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D65/00Wrappers or flexible covers; Packaging materials of special type or form
    • B65D65/38Packaging materials of special type or form
    • B65D65/46Applications of disintegrable, dissolvable or edible materials
    • B65D65/466Bio- or photodegradable packaging materials
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • 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
    • C08K5/0008Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/005Stabilisers against oxidation, heat, light, ozone
    • 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
    • C08K5/101Esters; Ether-esters of monocarboxylic acids
    • C08K5/105Esters; Ether-esters of monocarboxylic acids with phenols
    • 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
    • C08K5/16Nitrogen-containing compounds
    • C08K5/29Compounds containing one or more carbon-to-nitrogen double bonds
    • 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
    • C08K5/49Phosphorus-containing compounds
    • C08K5/51Phosphorus bound to oxygen
    • C08K5/52Phosphorus bound to oxygen only
    • C08K5/521Esters of phosphoric acids, e.g. of H3PO4
    • 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
    • C08K5/54Silicon-containing compounds
    • C08K5/541Silicon-containing compounds containing oxygen
    • C08K5/5415Silicon-containing compounds containing oxygen containing at least one Si—O bond
    • 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
    • C08L67/02Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2227Oxides; Hydroxides of metals of aluminium
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2237Oxides; Hydroxides of metals of titanium
    • C08K2003/2241Titanium dioxide
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/06Biodegradable
    • 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
    • Y02W90/00Enabling technologies or technologies with a potential or indirect contribution to greenhouse gas [GHG] emissions mitigation
    • Y02W90/10Bio-packaging, e.g. packing containers made from renewable resources or bio-plastics

Abstract

The present invention relates to an eco-friendly composition having improved biodegradability and processability, such as heat resistance, hydrolysis resistance and tensile strength, and capable of biodegradation in a natural state. Various products and containers for tables made of plastics can be substituted with those made by using the composition according to the present invention. In addition, the composition according to the present invention is degraded with ease by naturally occurring UV rays and microorganisms. Therefore, even when the products made by using the composition are allowed to stand in a natural state, after use, they are degraded naturally with no discharge of harmful substances to the air and soil, thereby preventing environmental pollution, one of the serious problems in the world. In addition, the composition according to the present invention shows higher strength and heat resistance, as compared to the eco-friendly resin compositions according to the related art, and thus can be applied to various industrial fields, including agriculture, fishery and food.

Description

생분해성 및 가공성이 향상된 친환경 조성물 및 이의 제조방법{Eco-friendly composition improved in biodegradability and plasticity and the preparation method thereof}Eco-friendly composition improved in biodegradability and plasticity and the preparation method thereof]

본 발명은 생분해성 및 가공성이 향상된 자연상태에서 생분해가 가능한 친환경 조성물에 관한 것으로서, 본 발명에서 제공하는 조성물을 사용함으로써 플라스틱을 이용하여 제조되는 각종 테이블용 제품 및 용기 등을 대체할 수 있다. 또한, 본 발명에서 제공하는 조성물은 자연상태에 존재하는 자외선 및 미생물 등에 의해서 분해가 용이하여서, 이를 이용하여 제조된 제품을 사용한 후에 자연상태로 방치하더라도 공기 및 토양에 유해물질을 배출하지 않고 자연스럽게 분해되므로 최근 세계적인 문제가 되는 환경오염을 방지할 수 있다.The present invention relates to an eco-friendly composition capable of biodegradation in a natural state with improved biodegradability and processability, and by using the composition provided in the present invention, various table products and containers manufactured using plastic can be replaced. In addition, the composition provided by the present invention is easily decomposed by ultraviolet rays and microorganisms existing in the natural state, so even if the product manufactured by using it is left in a natural state, it is naturally decomposed without emitting harmful substances to the air and soil. Therefore, it is possible to prevent environmental pollution, which is a recent global problem.

일반적인 합성수지는 내약품성, 내구성 및 여러 물성 등이 우수하여 천연소재의 대체물로 일상생활에 많이 사용되고 있으나, 사용 후 폐기시 자연으로 환원되지 못하는 단점이 있다. 특히, 수요가 급속하게 증가 되고 있는 일회용 포장재의 경우 분리수거가 원활히 이루어지지 않아 그대로 방치되는 경우가 많으며, 시골은 분리수거물품을 태우는 경우가 많아 환경에 많은 지장을 초래하고 있다.General synthetic resins are widely used in everyday life as a substitute for natural materials due to their excellent chemical resistance, durability, and various physical properties, but have a disadvantage in that they cannot be returned to nature when discarded after use. In particular, in the case of disposable packaging materials that are rapidly increasing in demand, separate collections are not performed smoothly and are often left unattended. In rural areas, separate collection items are often burned, causing many environmental problems.

또한, 종래에 상기 합성수지를 폐기시키는 방법으로는 폐기물을 연소시키거나, 토양에 매립하는 방법, 회수하여 재이용하는 방법 등을 사용하였으나 상기 합성수지 폐기물을 연소시키는 방법은 대량의 유독가스가 발생되어 2차 오염을 유발하는 문제점이 있으며, 매립방법 역시 분해되지 않고 토지에 그대로 남아 2차 오염을 야기하는 문제점이 있었고, 상기 회수하여 재이용하는 방법 역시 회수율이 낮아 최종 폐기물이 발생하는 문제점이 있었다.In addition, conventional methods for disposing of the synthetic resin include burning waste, embedding it in the soil, and recovering and reusing the waste. However, the method of burning synthetic resin waste generates a large amount of toxic gas, resulting in secondary There is a problem that causes pollution, and the landfill method is also not decomposed and remains in the land, causing secondary pollution, and the method of recovering and reusing also has a problem in that a final waste is generated due to a low recovery rate.

위와 같은 문제점을 해결하기 위해 미생물에 의해 분해되는 생분해성 수지를 이용하는 연구가 활발히 진행되고 있다. In order to solve the above problems, studies using biodegradable resins that are degraded by microorganisms are actively being conducted.

상기 생분해성 수지에는 미생물의 생체내에서 생합성되어 생분해성이 있는 폴리하이드록시아틸레이트계 수지, 폴리카프로락톤, 합성지방족 폴리에스테르수지 또는 열가소성 수지에 천연고분자 물질을 혼합한 수지 등이 있고, 이러한 생분해성 수지에 태양광에 의한 자연적인 분해가 가능한 광분해성 수지를 혼합하는 경우가 많은데, 상기 광분해성 수지에는 에틸렌과 일산화탄소를 공중합한 수지, 에틸렌과 비닐케톤을 공중합한 수지 및 전이금속 등 산화제를 첨가한 수지 등이 있다. 그러나 상기 수지 중 미생물이 생합성한 수지, 합성지방족 폴리에스테르 등은 분해성은 우수하나 제조가격이 비싼 단점이 있고, 천연고분자를 첨가한 수지는 가격은 저렴하나 물성저하 및 분해가 완전히 이루어지지 않으며, 내열성 및 내가수분해성이 낮고 또한 생분해성 및 가공성이 저하된다는 단점이 있다.The biodegradable resins include polyhydroxyatylate resins, polycaprolactones, synthetic aliphatic polyester resins, or resins in which a natural polymer material is mixed with a thermoplastic resin, which are biosynthesized and biodegradable in the body of microorganisms. Biodegradable resins are often mixed with photodegradable resins capable of natural decomposition by sunlight. The photodegradable resin contains oxidizing agents such as a resin copolymerized with ethylene and carbon monoxide, a resin copolymerized with ethylene and vinyl ketone, and a transition metal. And added resin. However, among the above resins, microbial-biosynthesized resins and synthetic aliphatic polyesters are excellent in degradability, but have a disadvantage in that the manufacturing price is high, and resins with natural polymers are inexpensive, but physical properties are not degraded and decomposed completely, and heat resistance. And there is a disadvantage in that the hydrolysis resistance is low and biodegradability and processability are deteriorated.

상기와 같은 문제점을 해결하기 위하여 본 발명자들은 내열성과 내가수분해성이 현저히 우수하면서도 생분해성 및 가공성이 우수하고 가격이 저렴하며 토양에 존재하는 미생물에 의해서 쉽게 분해될 수 있는 생분해성 수지와 천연물에서 쉽게 채취할 수 있는 자연상태의 고분자물질을 이용하여 종래의 플라스틱 제품을 대체할 수 있는 조성물을 발명하였고, 본 조성물을 이용하여 제조된 테이블용 제품이나 용기 등은 태양광의 자외선과 토양의 미생물에 의해서 자연스럽게 분해되므로 환경오염을 현저하게 저감할 수 있다.In order to solve the above problems, the present inventors have remarkably excellent heat resistance and hydrolysis resistance, but are excellent in biodegradability and processability, are inexpensive, and are easily degradable from biodegradable resins and natural products that can be easily decomposed by microorganisms present in the soil. Using a natural polymer material that can be collected, a composition that can replace conventional plastic products has been invented, and table products and containers manufactured using this composition are naturally produced by the ultraviolet rays of sunlight and microorganisms in the soil. Because it is decomposed, environmental pollution can be significantly reduced.

한국공개특허 제10-2015-0026368호Korean Patent Publication No. 10-2015-0026368 한국공개특허 제10-2012-0024628호Korean Patent Publication No. 10-2012-0024628

본 발명은 상기와 같은 문제점을 해결하기 위한 것으로서, 본 발명에서 제공하는 친환경 조성물 및 이를 이용한 친환경적 제품은 사용 후에 방치되었을 경우에 토양에 존재하는 미생물과 태양광에 의해서 자연적으로 분해되고 아울러 내열성 및 내가수분해성이 향상되어 최종 제품의 안정성을 현저히 향상시킬 수 있고, 종래의 플라스틱 제품을 처리하는 과정에서 발생하는 환경오염을 저감할 수 있고, 또한 무기물 등이 첨가되어 강도 및 가공성이 현저히 향상되었다. The present invention is to solve the above problems, and the eco-friendly composition and eco-friendly product using the same provided by the present invention are naturally decomposed by microorganisms present in the soil and sunlight when left unattended after use, and also heat resistance and The hydrolysis property is improved, so that the stability of the final product can be remarkably improved, the environmental pollution generated in the process of processing conventional plastic products can be reduced, and the strength and processability have been remarkably improved by adding inorganic substances.

본 발명의 또 다른 목적은 상기 생분해성 및 가공성이 향상된 친환경 조성물을 제조하는 방법을 제공하는 것이다.Another object of the present invention is to provide a method for preparing an eco-friendly composition with improved biodegradability and processability.

상기한 과제를 달성하기 위하여 본 발명에서 제공하는 상기 생분해성 및 가공성이 향상된 생분해성 친환경 조성물은 전처리된 녹말전분, 수산화알루미늄 분말, 카르보디이미드 화합물, 폴리락트산을 혼합하여 베이스 물질을 생성한 후에, 결정형 이산화티탄, 커플링제, 강화제, 열안정제, 산화방지제 등의 첨가제를 혼합하여 이루어진다.In order to achieve the above object, the biodegradable eco-friendly composition provided in the present invention with improved biodegradability and processability is prepared by mixing pretreated starch starch, aluminum hydroxide powder, carbodiimide compound, and polylactic acid to produce a base material, It is made by mixing additives such as crystalline titanium dioxide, a coupling agent, a reinforcing agent, a heat stabilizer, and an antioxidant.

또한, 상기 생분해성 친환경 조성물의 제조방법은 상기 전처리된 녹말과 수산화 알루미늄을 혼합하여 고온 교반하는 단계, 커플링제와 폴리락트산을 혼합하여 교반하는 단계, 결정형 이산화티탄, 강화제, 열안정제, 산화방지제 등을 혼합하여 교반하는 단계 및 상기 단계를 거친 최종 생성물을 자외선으로 처리하는 단계를 포함하여 이루어진다.In addition, the method for preparing the biodegradable eco-friendly composition includes mixing the pretreated starch and aluminum hydroxide and stirring at high temperature, mixing and stirring a coupling agent and polylactic acid, crystalline titanium dioxide, a reinforcing agent, a heat stabilizer, an antioxidant, etc. Mixing and stirring, and treating the final product passed through the above step with ultraviolet rays.

본 발명에서 제공하는 생분해성 및 가공성이 향상된 생분해성 친환경 조성물은 종래의 합성 플라스틱 조성물과 달리 자연상태에서 태양광 및 미생물에 의해서 분해가 가능하기 때문에 제품을 사용한 후에 처리하는 과정에서 발생하는 환경오염을 저감시킬 수 있고, 또한 종래의 생분해성 수지의 문제점이었던 강도가 낮고 가수분해성이 높아 가공성이 떨어진다는 문제점을 모두 해결할 수 있다.The biodegradable eco-friendly composition with improved biodegradability and processability provided by the present invention is capable of being decomposed by sunlight and microorganisms in a natural state, unlike conventional synthetic plastic compositions, thus reducing environmental pollution generated in the process of treatment after using the product. In addition, it is possible to reduce all the problems of low strength and high hydrolyzability, which were problems of conventional biodegradable resins, and thus poor processability.

또한, 본 발명에서 제공하는 조성물은 녹말의 함유가 상대적으로 높아 제조단가가 낮아 테이블용 식기 및 용기 등을 저렴한 가격으로 대량 공급할 수 있다는 장점이 있다.In addition, the composition provided by the present invention has the advantage of being able to supply large quantities of tableware and containers for a table at a low price due to a relatively high content of starch and low manufacturing cost.

또한, 본 발명의 전처리된 전분 함유 조성물을 각종 플라스틱류, 예를 들면 폴리에틸렌, 폴리프로필렌, 에틸렌-초산비닐 공중합체, 플리스티렌, ABS 수지, 폴리카보네이트, 폴리아미드, 폴리에스테르 등의 소수성 수지에 혼합함으로써 상기 소수성 수지에 흡습성을 부여하여 대전 방지성을 부여할 수도 있다.In addition, the pretreated starch-containing composition of the present invention is mixed with various plastics, such as polyethylene, polypropylene, ethylene-vinyl acetate copolymer, polystyrene, ABS resin, polycarbonate, polyamide, polyester, and other hydrophobic resins. By doing so, it is possible to impart hygroscopicity to the hydrophobic resin to impart antistatic properties.

이하에서는 본 발명에서 제공하고자 하는 생분해성 친환경 조성물에 대하여 자세히 설명한다.Hereinafter, a biodegradable eco-friendly composition to be provided in the present invention will be described in detail.

본 발명에서 제공하는 친환경 조성물은 전처리된 녹말 전분 100 중량부에 대하여 수산화알루미늄 30 내지 50 중량부, 폴리락트산 20 내지 50 중량부, 카르보디이미드 화합물 20 내지 50 중량부, 이산화티탄 결정 0.2 내지 2 중량부, 커플링제 5 내지 10 중량부, 강화제 5 내지 10 중량부, 열안정제 2 내지 5 중량부 및 산화방지제 0.2 내지 2 중량부로 구성되는 것이 바람직하다.The eco-friendly composition provided by the present invention is 30 to 50 parts by weight of aluminum hydroxide, 20 to 50 parts by weight of polylactic acid, 20 to 50 parts by weight of carbodiimide compound, 0.2 to 2 parts by weight of titanium dioxide crystals based on 100 parts by weight of pretreated starch starch Parts, 5 to 10 parts by weight of a coupling agent, 5 to 10 parts by weight of a reinforcing agent, 2 to 5 parts by weight of a heat stabilizer, and 0.2 to 2 parts by weight of an antioxidant.

상기 전처리된 녹말전분은 천연물로부터 수득된 녹말을 전처리한 산화 전분, 카복시메틸 전분, 하이드록시알킬 전분, 에스테르화 전분, 초산 전분, 인산 전분 등을 사용하는 것이 바람직하고, 또한 폴리아크릴산, 폴리초산비닐, 폴리아크릴아미드, 폴리아크릴로니트릴 등을 그래프트한 그래프트화 전분을 사용하는 것이 바람직하다.The pretreated starch starch is preferably oxidized starch, carboxymethyl starch, hydroxyalkyl starch, esterified starch, starch acetate, starch phosphate, etc., obtained by pre-treating starch obtained from natural products, and also polyacrylic acid, polyvinyl acetate , Polyacrylamide, polyacrylonitrile, and the like are preferably grafted to use grafted starch.

본 발명에서 사용되는 수산화알루미늄은 백색의 분말을 사용하고, 녹말전분과 폴리락트산 및 카르보디이미드 화합물의 결합을 촉진하는 촉매의 역할을 하며, 아울러 최종 조성물의 기계적 강도를 향상시키는 기능을 한다.The aluminum hydroxide used in the present invention uses a white powder, serves as a catalyst for promoting the bonding of starch starch, polylactic acid and carbodiimide compounds, and also functions to improve the mechanical strength of the final composition.

본 발명에서 사용되는 카르보디이미드 화합물은 폴리카르보디이미드 화합물을 포함하여 분자 내에 적어도 하나의 카르보디이미드기를 가지고 있는 화합물이면 바람직하고, 상기 카르보디이미드 화합물의 구체적인 예로서는 디시클로헥실카르보디이미드, 디이소프로필카르보디이미드, 디메틸카르보디이미드, 디이소부틸카르보디이미드, 디옥틸카르보디이미드, t-부틸이소프The carbodiimide compound used in the present invention is preferably a compound having at least one carbodiimide group in the molecule, including a polycarbodiimide compound. Specific examples of the carbodiimide compound include dicyclohexylcarbodiimide and di Isopropylcarbodiimide, dimethylcarbodiimide, diisobutylcarbodiimide, dioctylcarbodiimide, t-butylisope

로필카르보디이미드, 디페닐카르보디이미드, 디-t-부틸카르보디이미드 및 디-β-나프틸카르보디이미드 등이 특히 바람직하다.Particularly preferred are lopilcarbodiimide, diphenylcarbodiimide, di-t-butylcarbodiimide and di-β-naphthylcarbodiimide.

상기 카르보디이미드화합물의 함량은 전처리된 녹말전분 100 중량부 대비 20 내지 50 중량부가 바람직하여, 카르보디이미드화합물의 함량이 20 중량부 미만일 때에는 조성물의 생분해성 및 가공성의 향상이 현저하지 못하고, 50 중량부를 초과할 경우에는 조성물의 투명성이 저하될 수 있다.The content of the carbodiimide compound is preferably 20 to 50 parts by weight based on 100 parts by weight of the pretreated starch starch, and when the content of the carbodiimide compound is less than 20 parts by weight, the biodegradability and processability of the composition is not significantly improved, and 50 When it exceeds a part by weight, the transparency of the composition may decrease.

상기 커플링제는 3메틸에톡시실란, 메틸트리메톡시실란, 페닐트리메톡시실란 등 실란계 화합물이 사용될 수 있다. 상기 커플링제의 함량은 상기 전처리된 녹말전분 100 중량부에 대하여 5 내지 10 중량부를 사용하는 것이 바람직하다. 커플링제가 5 중량부보다 낮을 때에는 최종 생성되는 제품의 내가수분해성 및 열안정성이 저하될 우려가 있고, 10 중량부를 초과할 경우에는 조성물의 가공성이 저하될 우려가 있다.The coupling agent may be a silane-based compound such as 3methylethoxysilane, methyltrimethoxysilane, or phenyltrimethoxysilane. The content of the coupling agent is preferably 5 to 10 parts by weight based on 100 parts by weight of the pretreated starch starch. When the coupling agent is less than 5 parts by weight, the hydrolysis resistance and thermal stability of the final product may be deteriorated, and when it exceeds 10 parts by weight, the processability of the composition may be lowered.

상기 이산화티탄 결정은 아나타제형의 결정형을 사용하는 것이 바람직하고, 실란 화합물로 표면처리되는 것이 더욱 바람직한데, 상기 이산화티탄을 표면처리하기 위한 실란 화합물로서는 γ-암모니아 프로필 메틸 2-에톡시 실란을 사용하는 것이 바람직하다. 상기 이산화티탄 결정은 태양광을 조사받았을 경우에 다양한 종류의 박테리아 등을 살균하는 기능을 가지고 있어서, 본 친환경 조성물을 이용하여 식품용기를 제조하였을 경우에 상기 식품용기가 인체에 유해한 미생물에 의해서 오염되는 것을 방지할 수 있다.The titanium dioxide crystal is preferably an anatase-type crystal form, more preferably surface-treated with a silane compound, and γ-ammonia propyl methyl 2-ethoxy silane is used as a silane compound for surface treatment of the titanium dioxide. It is desirable to do. The titanium dioxide crystal has a function of sterilizing various kinds of bacteria, etc. when irradiated with sunlight, so when a food container is manufactured using this eco-friendly composition, the food container is contaminated by microorganisms harmful to the human body. Can be prevented.

상기 이산화티탄 결정은 전처리된 녹말전분 100 중량부에 대하여 0.2 내지 2 중량부를 사용하는 것이 바람직하다. 이산화티탄 함량이 상기 범위를 벗어날 경우에는 최종 조성물의 가공성이 저하될 우려가 있다.It is preferable to use 0.2 to 2 parts by weight of the titanium dioxide crystal based on 100 parts by weight of the pretreated starch starch. If the titanium dioxide content is out of the above range, there is a concern that the processability of the final composition is deteriorated.

상기 강화제는 본 친환경 조성물을 이용하여 제품을 제조하였을 경우에 제품의 물리적인 강도를 향상시키는 효과가 있는데, 이러한 강화제로서는 활석 등의 무기물이 사용될 수 있다. 상기 활석은 흡수성 및 고착성이 강하고 내화성이 좋아서 다양한 종류의 충진제로서 사용되고 있어서 본 친환경 조성물의 열저항성과 강도를 향상시키는 데에 적합한 물질이다.The reinforcing agent has an effect of improving the physical strength of the product when the product is manufactured using the eco-friendly composition, and inorganic substances such as talc may be used as the reinforcing agent. The talc is a material suitable for improving the heat resistance and strength of the eco-friendly composition because it is used as various types of fillers because of its strong absorbency and adhesion and good fire resistance.

상기 강화제의 함량은 전처리된 녹말전분 100 중량부에 대하여 5 내지 10 중량부를 사용하는 것이 바람직하다. 강화제의 함량이 5 중량부 이하일 경우에는 최종 생성물의 강도가 저하되며, 10 중량부를 초과하는 경우에는 최종 생성물의 가공성이 저하된다.The content of the reinforcing agent is preferably 5 to 10 parts by weight based on 100 parts by weight of the pretreated starch starch. When the content of the reinforcing agent is 5 parts by weight or less, the strength of the final product decreases, and when it exceeds 10 parts by weight, the processability of the final product decreases.

상기 산화방지제는 본 발명의 친환경 조성물을 이용하여 식품용기 등 제품을 생산하였을 때에 상기 제품이 공기중의 산소에 의해서 자동산화되는 것을 방지하기 위한 것으로서 레몬산 수지, 페놀형 산화방지제 또는 포스페이트형 산화방지제를 사용할 수 있다. 상기 페놀형 산화방지제로서는 4,4'-메틸렌-비스(2,6-디-t-부틸페놀), 옥타데실-3-(3,5-디-t-부틸-4-히드록시페닐)프로피오네이트, 펜타에리트리톨테트라키스(3-(3,5-디-t-부틸-4-히드록시페닐))프로피오네이트 등이 사용될 수 있고, 상기 포스페이트형 산화방지제로서는 트리스(2,4-디-t-부틸페닐)포스페이트 또는 비스(2,4-디-t-부틸페닐펜타에리트리톨)디포스페이트 등이 사용될 수 있다.The antioxidant is to prevent the product from being automatically oxidized by oxygen in the air when a product such as a food container is produced using the eco-friendly composition of the present invention, and a lemon acid resin, a phenolic antioxidant, or a phosphate-type antioxidant is used. Can be used. As the phenolic antioxidant, 4,4'-methylene-bis(2,6-di-t-butylphenol), octadecyl-3-(3,5-di-t-butyl-4-hydroxyphenyl)pro Cypionate, pentaerythritol tetrakis (3-(3,5-di-t-butyl-4-hydroxyphenyl)) propionate, etc. may be used, and as the phosphate-type antioxidant, tris (2,4- Di-t-butylphenyl)phosphate or bis(2,4-di-t-butylphenylpentaerythritol)diphosphate and the like may be used.

상기 산화방지제의 함량은 전처리된 녹말전분 100 중량부 대비 0.2 내지 2 중량부를 사용하는 것이 바람직하고, 산화방지제의 함량이 상기 범위를 벗어나는 경우에는 최종 조성물의 투명성과 내열성이 저하될 우려가 있다.The content of the antioxidant is preferably 0.2 to 2 parts by weight based on 100 parts by weight of the pretreated starch starch, and when the content of the antioxidant is outside the above range, there is a concern that the transparency and heat resistance of the final composition may be lowered.

본 발명에서 사용되는 상기 열안정제는 본 발명의 조성물을 이용하여 제품을 제조하는 가공공정에서 발생할 수 있는 열열화, 광열화 및 산화열화 등을 방지 및 억제하기 위한 것으로서, 상기 열안정제로서는 주석, 칼슘, 아연 등이 사용될 수 있다.The thermal stabilizer used in the present invention is to prevent and suppress thermal deterioration, photo deterioration, and oxidative deterioration that may occur in the processing process of manufacturing a product using the composition of the present invention, and as the thermal stabilizer, tin, calcium , Zinc, and the like may be used.

상기 성분들 이외에서 본 발명의 조성물은 본 발명의 효과를 손상시키지 않는 범위내에서, 선택적으로 윤활제, 왁스, 착색제, 결정화 촉진제, 광안정화제 또는 자외선 흡수제 등의 기타 첨가제들을 사용할 수 있다.In addition to the above components, the composition of the present invention may optionally use other additives such as a lubricant, a wax, a colorant, a crystallization accelerator, a light stabilizer or an ultraviolet absorber within the range not impairing the effect of the present invention.

본 발명의 생분해성 플라스틱 조성물은 생분해율을 안정적으로 조절하고, 내가수분해성 및 내열성을 향상시키며, 투명성을 유지할 수 있으므로, 농업, 임업 및 어업용 재료(필름, 시트, 식목 용기, 낚싯줄, 그물 등), 토목 작업용 재료(묘목용 망, 샌드백 등), 식품을 보관하기 위한 용기 및 포장, 특히 필름, 시트, 섬유, 병 및 접시 등과 같은 생분해성 플라스틱 성형물 등에 적합하게 사용될 수 있다.The biodegradable plastic composition of the present invention stably controls the biodegradation rate, improves hydrolysis resistance and heat resistance, and can maintain transparency, and thus materials for agriculture, forestry and fishing (film, sheet, planting container, fishing line, net, etc.) , Civil engineering materials (seedling nets, sandbags, etc.), containers and packaging for storing food, especially biodegradable plastic moldings such as films, sheets, fibers, bottles and plates, etc.

본 발명의 또 다른 목적은 본 발명의 친환경 조성물을 제조하는 방법을 제공하는 것이다. 본 발명의 조성물을 제조하는 방법은 아래의 단계를 포함하여 구성된다.Another object of the present invention is to provide a method of preparing the eco-friendly composition of the present invention. The method of preparing the composition of the present invention comprises the following steps.

본 발명의 친환경 조성물을 제조하는 단계는;Preparing the eco-friendly composition of the present invention;

전처리된 녹말전분과 전처리된 녹말전분 100 중량부 대비 물 100 내지 200 중량부를 혼합하여 녹말 농축용액을 제조하는 단계;Preparing a starch concentrate solution by mixing 100 to 200 parts by weight of water based on 100 parts by weight of the pretreated starch starch and the pretreated starch starch;

상기 녹말 농축용액과 전처리된 녹말전분 100 중량부 대비 수산화알루미늄 30 내지 50 중량부를 혼합한 후에 130 내지 140 ℃에서 10분 내지 20분 동안 교반하는 단계;Mixing the concentrated starch solution and 30 to 50 parts by weight of aluminum hydroxide based on 100 parts by weight of the pretreated starch starch and then stirring at 130 to 140° C. for 10 to 20 minutes;

상기 단계의 혼합물에 폴리락트산, 카르보디이미드 화합물 및 실란 커플링제를 혼합하여 30분 내지 1 시간 동안 교반하는 단계;Mixing a polylactic acid, a carbodiimide compound, and a silane coupling agent in the mixture of the above step and stirring for 30 minutes to 1 hour;

상기 단계에서 생성된 조성물에 실란 화합물로 표면 처리된 이산화티탄 결정, 강화제, 열안정제 및 산화방지제를 혼합하여 1 시간 내지 2 시간 동안 교반하는 단계;Mixing a titanium dioxide crystal surface-treated with a silane compound, a reinforcing agent, a heat stabilizer, and an antioxidant in the composition produced in the above step and stirring for 1 to 2 hours;

상기 단계에서 생성된 조성물을 자외선을 이용하여 소독한 후에 10 내지 20 ℃에서 2 시간 내지 3 시간 동안 냉각하는 단계;로 구성된다.After disinfecting the composition produced in the above step using ultraviolet rays, cooling the composition at 10 to 20° C. for 2 to 3 hours; consists of.

본 발명의 친환경 조성물을 제조하는 방법은 상기 이산화티탄 결정, 강화제, 열안정제 및 산화방지제를 혼합하여 교반하는 단계에 선택적으로 윤활제, 왁스, 착색제, 광안정화제 및 자외선 흡수제 등을 더 첨가하여 교반할 수 있다.The method for preparing the eco-friendly composition of the present invention can be stirred by optionally adding a lubricant, wax, colorant, light stabilizer and ultraviolet absorber to the step of mixing and stirring the titanium dioxide crystal, reinforcing agent, heat stabilizer and antioxidant. have.

이하 본 발명의 실시예를 통하여 본 발명을 더욱 상세히 설명하지만, 본 발명의 범주가 하기 실시예에 의해서 한정되는 것은 아니다.Hereinafter, the present invention will be described in more detail through examples of the present invention, but the scope of the present invention is not limited by the following examples.

아래의 실시예에서 전분은 녹말 전분을 의미한다.In the examples below, starch means starch starch.

<실시예 1><Example 1>

초산 전분 100g을 물 150g과 혼합하여 녹말 농축액을 제조한 후, 여기에 수산화알루미늄 30g을 혼합하여 130℃에서 10분 동안 교반하여 혼합물을 수득한다.After preparing a starch concentrate by mixing 100 g of starch acetate with 150 g of water, 30 g of aluminum hydroxide was mixed thereto and stirred at 130° C. for 10 minutes to obtain a mixture.

상기 혼합물에 폴리락트산 30g, 디시클로헥실카르보디이미드 30g 및 메틸트리메톡시실란 5g을 첨가한 후에 130℃에서 1 시간 동안 교반한다.After adding 30 g of polylactic acid, 30 g of dicyclohexylcarbodiimide and 5 g of methyltrimethoxysilane to the mixture, the mixture was stirred at 130° C. for 1 hour.

상기 혼합물에 이산화티탄 결정 1g, 활석 8g, 주석 3g, 레몬산수지 1g을 첨가하여 130℃에서 1시간 동안 교반한다.To the mixture was added 1 g of titanium dioxide crystals, 8 g of talc, 3 g of tin, and 1 g of lemon acid resin, followed by stirring at 130°C for 1 hour.

상기에서 수득된 조성물을 130℃에서 자외선을 가하여 소독한 후에 20℃에서 3시간 동안 냉각하여 조성물을 수득하였다.The composition obtained above was sterilized by applying ultraviolet rays at 130° C. and then cooled at 20° C. for 3 hours to obtain a composition.

<실시예 2><Example 2>

하이드록시알킬 전분 100g을 물 150g과 혼합하여 녹말 농축액을 제조한 후, 여기에 수산화알루미늄 30g을 혼합하여 130℃에서 10분 동안 교반하여 혼합물을 수득한다.After mixing 100 g of hydroxyalkyl starch with 150 g of water to prepare a starch concentrate, 30 g of aluminum hydroxide was mixed thereto and stirred at 130° C. for 10 minutes to obtain a mixture.

상기 혼합물에 폴리락트산 30g, 디이소프로필카르보디이미드 30g 및 페닐트리메톡시실란 5g을 첨가한 후에 130℃에서 1 시간 동안 교반한다.After adding 30 g of polylactic acid, 30 g of diisopropylcarbodiimide, and 5 g of phenyltrimethoxysilane to the mixture, the mixture was stirred at 130° C. for 1 hour.

상기 혼합물에 이산화티탄 결정 1g, 활석 8g, 아연 3g, 4,4'-메틸렌-비스(2,6-디-t-부틸페놀) 1g을 첨가하여 130℃에서 1시간 동안 교반한다.To the mixture, 1 g of titanium dioxide crystals, 8 g of talc, 3 g of zinc, and 1 g of 4,4'-methylene-bis(2,6-di-t-butylphenol) were added, followed by stirring at 130° C. for 1 hour.

상기에서 수득된 조성물을 130℃에서 자외선을 가하여 소독한 후에 20℃에서 3시간 동안 냉각하여 조성물을 수득하였다.The composition obtained above was sterilized by applying ultraviolet rays at 130° C. and then cooled at 20° C. for 3 hours to obtain a composition.

<실시예 3><Example 3>

카복시메틸 전분 100g을 물 150g과 혼합하여 녹말 농축액을 제조한 후, 여기에 수산화알루미늄 30g을 혼합하여 130℃에서 10분 동안 교반하여 혼합물을 수득한다.After mixing 100 g of carboxymethyl starch with 150 g of water to prepare a starch concentrate, 30 g of aluminum hydroxide was mixed thereto, followed by stirring at 130° C. for 10 minutes to obtain a mixture.

상기 혼합물에 폴리락트산 30g, 디메틸카르보디이미드 30g 및 페닐트리메톡시실란 5g을 첨가한 후에 130℃에서 1 시간 동안 교반한다.After adding 30 g of polylactic acid, 30 g of dimethylcarbodiimide and 5 g of phenyltrimethoxysilane to the mixture, the mixture was stirred at 130° C. for 1 hour.

상기 혼합물에 이산화티탄 결정 1g, 활석 8g, 아연 3g, 트리스(2,4-디-t-부틸페닐)포스페이트 1g을 첨가하여 130℃에서 1시간 동안 교반한다.1 g of titanium dioxide crystals, 8 g of talc, 3 g of zinc, and 1 g of tris(2,4-di-t-butylphenyl)phosphate were added to the mixture, followed by stirring at 130°C for 1 hour.

상기에서 수득된 조성물을 130℃에서 자외선을 가하여 소독한 후에 20℃에서 3시간 동안 냉각하여 조성물을 수득하였다.The composition obtained above was sterilized by applying ultraviolet rays at 130° C. and then cooled at 20° C. for 3 hours to obtain a composition.

<실시예 4><Example 4>

인산 전분 100g을 물 150g과 혼합하여 녹말 농축액을 제조한 후, 여기에 수산화알루미늄 30g을 혼합하여 130℃에서 10분 동안 교반하여 혼합물을 수득한다.After preparing a starch concentrate by mixing 100 g of starch phosphate with 150 g of water, 30 g of aluminum hydroxide was mixed thereto and stirred at 130° C. for 10 minutes to obtain a mixture.

상기 혼합물에 폴리락트산 30g, 디이소프로필카르보디이미드 30g 및 페닐트리메톡시실란 5g을 첨가한 후에 130℃에서 50분 동안 교반한다.To the mixture was added 30 g of polylactic acid, 30 g of diisopropylcarbodiimide, and 5 g of phenyltrimethoxysilane, followed by stirring at 130° C. for 50 minutes.

상기 혼합물에 이산화티탄 결정 1g, 활석 8g, 아연 3g, 펜타에리트리톨테트라키스(3-(3,5-디-t-부틸-4-히드록시페닐))프로피오네이트 1g을 첨가하여 130℃에서 1시간 동안 교반한다.To the mixture was added 1 g of titanium dioxide crystals, 8 g of talc, 3 g of zinc, and 1 g of pentaerythritol tetrakis (3-(3,5-di-t-butyl-4-hydroxyphenyl)) propionate at 130° C. Stir for 1 hour.

상기에서 수득된 조성물을 130℃에서 자외선을 가하여 소독한 후에 20℃에서 3시간 동안 냉각하여 조성물을 수득하였다.The composition obtained above was sterilized by applying ultraviolet rays at 130° C. and then cooled at 20° C. for 3 hours to obtain a composition.

상기 실시예 1 내지 4를 통해서 수득된 본 발명의 친환경 조성물을 이용하여 시편(가로 10 cm, 세로 10 cm)을 제작한 후에 각 시편의 생분해효율, 인장강도 및 내열성을 시험하여 표 1에 나타내었다. After preparing a specimen (10 cm wide, 10 cm long) using the eco-friendly composition of the present invention obtained through Examples 1 to 4, the biodegradation efficiency, tensile strength and heat resistance of each specimen were tested and shown in Table 1. .

상기 생분해 효율 실험은 ISO14855에서 특정된 바와 같이 실시하여 제어가능한 혼합 조건하에서 산소 요구 생분해 효율 및 생성된 CO2양의 분석을 위한 구조 파괴 효율을 측정하였다. ISO14855에 따르면, 총 분해성 피브린을 플라스틱 물질 분해실험에서 참고 물질로 사용하였다. 실험 45일 후, 참고물질의 분해율이 70%보다 더 클 때 상기 분해는 완전히 분해된 것으로 간주하였다. 일반적으로 분해성 폴리에틸렌 필름은 분해율이 20% 미만이어서는 안되고, 패키징 제품의 경우에는 15% 미만이어서는 안된다고 알려져 있다. 본 실험결과에 의하면 본 발명의 조성물은 완전 생분해성이라고 할 수 있다.The biodegradation efficiency experiment was conducted as specified in ISO14855 to measure the oxygen demand biodegradation efficiency and the structure destruction efficiency for the analysis of the amount of CO2 produced under controllable mixing conditions. According to ISO14855, total degradable fibrin was used as a reference material in plastic material decomposition experiments. After 45 days of the experiment, when the decomposition rate of the reference material was greater than 70%, the decomposition was considered to be completely decomposed. In general, it is known that the degradable polyethylene film should not have a decomposition rate of less than 20%, and should not be less than 15% for packaging products. According to the results of this experiment, the composition of the present invention can be said to be completely biodegradable.

내가수분해성에 대한 시험은 80℃ 및 90% RH에서 각각 유지되는 대기 조성 챔버내에 시편들을 일정 기간(100 시간) 동안 놓고, 테스트 전의 값에 대해 테스트 후의 인장 강도의 비율(%)을 계산하였다. 높은 인장 강도의 비율(80% 이상)을 가진 샘플에 대해 내가수분해성을 '좋음'으로 정하였다.In the test for hydrolysis resistance, the specimens were placed in an atmospheric composition chamber maintained at 80° C. and 90% RH, respectively, for a certain period (100 hours), and the ratio (%) of the tensile strength after the test to the value before the test was calculated. For samples with a high tensile strength ratio (80% or more), the hydrolysis resistance was set as'good'.

인장강도 시험은 아령형 시편을 제조하여 시험하였고, 내열성시험은 시편들을 100℃의 열수에 5시간 동안 넣고 테스트 전의 값에 대해 테스트 후의 인장강도의 비율을 계산하였으며, 80%이상의 높은 인장강도의 비율을 가진 샘플에 대해서 내열성을 ‘좋음’으로 정하였다.For the tensile strength test, a dumbbell-shaped specimen was prepared and tested, and in the heat resistance test, the specimens were placed in hot water at 100°C for 5 hours and the ratio of the tensile strength after the test was calculated with respect to the value before the test, and the ratio of high tensile strength of 80% or more. The heat resistance was set as'good' for the sample having

투명성에 대한 시험은 JIS K7105 '플라스틱의 광학 특성 평가법', 6.4 '헤이즈(흐림도: cloudiness)'에 따라 헤이즈기(haze meter)를 사용하여 필름 시편의 헤이즈(흐림도)를 측정하였다. 낮은 헤이즈(10% 이하)를 가진 샘플에 대해 투명성을 '좋음'으로 정하였다.In the test for transparency, the haze (cloudiness) of the film specimen was measured using a haze meter according to JIS K7105'Evaluation Method of Optical Properties of Plastics', 6.4'Haze (cloudiness)'. For samples with low haze (less than 10%), transparency was set as'good'.

구분division 실시예 1Example 1 실시예 2Example 2 실시예 3Example 3 실시예 4Example 4 생분해율(%)Biodegradation rate (%) 88.588.5 89.289.2 91.691.6 93.193.1 인장강도(MPa)Tensile strength (MPa) 51.251.2 53.353.3 52.552.5 55.155.1 내가수분해성(%)Hydrolysis resistance (%) 좋음(89.1)Good(89.1) 좋음(89.5)Good(89.5) 좋음(90.1)Good(90.1) 좋음(91.1)Good(91.1) 내열성(%)Heat resistance (%) 좋음(92)Good(92) 좋음(90)Good(90) 좋음(91)Good(91) 좋음(91)Good(91) 투명도(%)transparency(%) 좋음(2.5)Good(2.5) 좋음(3.3)Good(3.3) 좋음(2.7)Good(2.7) 좋음(3.6)Good(3.6)

상기의 표 1에 제시된 결과에 나타난 바와 같이, 본 발명에서 제공하는 친환경 조성물은 생분해성과 내열성, 내가수분해성, 인장강도 등 가공성이 우수하여 종래의 플라스틱 제품 등을 대체할 수 있고, 생분해율이 높아서 자연상태에 방지하여도 태양광과 미생물에 의해서 분해될 수 있어 환경오염을 방지할 수 있으므로, 향후 다양한 플라스틱 제품을 대체할 수 있다.As shown in the results shown in Table 1 above, the eco-friendly composition provided by the present invention has excellent processability such as biodegradability, heat resistance, hydrolysis resistance, and tensile strength, so that it can replace conventional plastic products, and has a high biodegradation rate. Even if it is prevented in natural conditions, it can be decomposed by sunlight and microorganisms to prevent environmental pollution, so it can replace various plastic products in the future.

본 발명은 산업상 이용가능하다.The present invention is industrially applicable.

Claims (11)

삭제delete 삭제delete 삭제delete 삭제delete 삭제delete 자연적인 분해가 가능한 조성물의 제조방법에 대한 것으로서 상기 제조방법은;
전처리된 녹말 전분과 전처리된 녹말 전분 100 중량부 대비 물 100 내지 200 중량부를 혼합하여 녹말 농축용액을 제조하는 단계;
상기 녹말 농축용액과 전처리된 녹말 전분 100 중량부 대비 수산화알루미늄 30 내지 50 중량부를 혼합한 후에 130 내지 140 ℃에서 10분 내지 20분 동안 교반하는 단계;
상기 단계의 혼합물에 폴리락트산, 카르보디이미드 화합물 및 실란 커플링제를 혼합하여 30분 내지 1 시간 동안 교반하는 단계;
상기 단계에서 생성된 조성물에 실란 화합물로 표면 처리된 이산화티탄 결정, 강화제, 열안정제 및 산화방지제를 혼합하여 1 시간 내지 2 시간 동안 교반하는 단계;
상기 단계에서 생성된 조성물을 자외선을 이용하여 소독한 후에 10 내지 20 ℃에서 2 시간 내지 3 시간 동안 냉각하는 단계;로 이루어지는 것을 특징으로 하는 조성물의 제조방법
As for a method for preparing a composition capable of natural decomposition, the method includes;
Preparing a starch concentrate solution by mixing 100 to 200 parts by weight of water based on 100 parts by weight of the pretreated starch starch and the pretreated starch starch;
Mixing the concentrated starch solution with 30 to 50 parts by weight of aluminum hydroxide based on 100 parts by weight of the pretreated starch starch and then stirring at 130 to 140° C. for 10 to 20 minutes;
Mixing a polylactic acid, a carbodiimide compound, and a silane coupling agent to the mixture of the above step and stirring for 30 minutes to 1 hour;
Mixing a titanium dioxide crystal surface-treated with a silane compound, a reinforcing agent, a heat stabilizer, and an antioxidant in the composition produced in the above step and stirring for 1 to 2 hours;
After disinfecting the composition produced in the above step by using ultraviolet rays, cooling the composition at 10 to 20° C. for 2 to 3 hours; a method for preparing a composition comprising:
제6항에 있어서, 상기 카르보디이미드 화합물은 디시클로헥실카르보디이미드, 디이소프로필카르보디이미드, 디메틸카르보디이미드, 디이소부틸카르보디이미드, 디옥틸카르보디이미드, t-부틸이소프로필카르보디이미드, 디페닐카르보디이미드, 디-t-부틸카르보디이미드 및 디-β-나프틸카르보디이미드 중에서 선택된 어느 하나인 것을 특징으로 하는 조성물의 제조방법The method of claim 6, wherein the carbodiimide compound is dicyclohexylcarbodiimide, diisopropylcarbodiimide, dimethylcarbodiimide, diisobutylcarbodiimide, dioctylcarbodiimide, t-butylisopropylcar Method for producing a composition, characterized in that any one selected from bodyimide, diphenylcarbodiimide, di-t-butylcarbodiimide, and di-β-naphthylcarbodiimide 제6항에 있어서, 상기 커플링제는 3메틸에톡시실란, 메틸트리메톡시실란 및 페닐트리메톡시실란 중에서 선택된 어느 하나인 것을 특징으로 하는 조성물의 제조방법The method of claim 6, wherein the coupling agent is any one selected from 3methylethoxysilane, methyltrimethoxysilane, and phenyltrimethoxysilane. 제6항에 있어서, 상기 산화방지제는 4,4'-메틸렌-비스(2,6-디-t-부틸페놀), 옥타데실-3-(3,5-디-t-부틸-4-히드록시페닐)프로피오네이트, 펜타에리트리톨테트라키스(3-(3,5-디-t-부틸-4-히드록시페닐))프로피오네이트, 트리스(2,4-디-t-부틸페닐)포스페이트 또는 비스(2,4-디-t-부틸페닐펜타에리트리톨)디포스페이트 중에서 선택된 어느 하나인 것을 특징으로 하는 조성물의 제조방법The method of claim 6, wherein the antioxidant is 4,4'-methylene-bis(2,6-di-t-butylphenol), octadecyl-3-(3,5-di-t-butyl-4-hydro Roxyphenyl) propionate, pentaerythritol tetrakis (3-(3,5-di-t-butyl-4-hydroxyphenyl)) propionate, tris (2,4-di-t-butylphenyl) Phosphate or bis (2,4-di-t-butylphenylpentaerythritol) diphosphate method for producing a composition, characterized in that any one selected from 제6항에 있어서, 상기 전처리된 녹말 전분은 산화 전분, 카복시메틸 전분, 하이드록시알킬 전분, 에스테르화 전분, 초산 전분, 인산 전분 중에서 선택되는 어느 하나인 것을 특징으로 하는 조성물의 제조방법

The method of claim 6, wherein the pretreated starch starch is any one selected from oxidized starch, carboxymethyl starch, hydroxyalkyl starch, esterified starch, acetic acid starch, and phosphate starch.

삭제delete
KR1020190119231A 2019-09-27 2019-09-27 Eco-friendly composition improved in biodegradability and plasticity and the preparation method thereof KR102191338B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1020190119231A KR102191338B1 (en) 2019-09-27 2019-09-27 Eco-friendly composition improved in biodegradability and plasticity and the preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1020190119231A KR102191338B1 (en) 2019-09-27 2019-09-27 Eco-friendly composition improved in biodegradability and plasticity and the preparation method thereof

Publications (1)

Publication Number Publication Date
KR102191338B1 true KR102191338B1 (en) 2020-12-16

Family

ID=74041998

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1020190119231A KR102191338B1 (en) 2019-09-27 2019-09-27 Eco-friendly composition improved in biodegradability and plasticity and the preparation method thereof

Country Status (1)

Country Link
KR (1) KR102191338B1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113429760A (en) * 2021-07-16 2021-09-24 浙江永韬新材料有限公司 Express bag degradation particles and preparation method thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4414415B2 (en) * 2006-07-19 2010-02-10 昭和高分子株式会社 Biodegradable resin composition and biodegradable film
KR20120024628A (en) 2009-04-23 2012-03-14 래니어 리미티드 Vertebral surface preparation instrument
KR20140007859A (en) * 2011-02-24 2014-01-20 도레이 카부시키가이샤 Polylactic acid-based film
JP2014523960A (en) * 2011-07-29 2014-09-18 シャンハイ ザイホーア インダストリアル インベストメント カンパニー リミテッド New biodegradable masterbatch and preparation method
KR101495367B1 (en) * 2007-02-23 2015-02-24 데이진 가부시키가이샤 Polylactic acid composition
KR20150026368A (en) 2013-09-02 2015-03-11 삼성정밀화학 주식회사 Method of preparing biodegradable polyester resin

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4414415B2 (en) * 2006-07-19 2010-02-10 昭和高分子株式会社 Biodegradable resin composition and biodegradable film
KR101495367B1 (en) * 2007-02-23 2015-02-24 데이진 가부시키가이샤 Polylactic acid composition
KR20120024628A (en) 2009-04-23 2012-03-14 래니어 리미티드 Vertebral surface preparation instrument
KR20140007859A (en) * 2011-02-24 2014-01-20 도레이 카부시키가이샤 Polylactic acid-based film
JP2014523960A (en) * 2011-07-29 2014-09-18 シャンハイ ザイホーア インダストリアル インベストメント カンパニー リミテッド New biodegradable masterbatch and preparation method
KR20150026368A (en) 2013-09-02 2015-03-11 삼성정밀화학 주식회사 Method of preparing biodegradable polyester resin

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113429760A (en) * 2021-07-16 2021-09-24 浙江永韬新材料有限公司 Express bag degradation particles and preparation method thereof

Similar Documents

Publication Publication Date Title
RU2480495C2 (en) Novel biodegradable polymer composition suitable for producing biodegradable plastic, and method of preparing said composition
EP1725614B1 (en) Biodegradable compositions comprising polylactic polymers, adipat copolymers and magnesium silicate
US5135966A (en) Environmentally degradable polymer composition
US20230340238A1 (en) Biodegradable resin composition and production method therefor
KR101184750B1 (en) Control of biodegradability of polyvinyl alchol and cellulose polymer mixed polymer films and the preparation thereof
Rizzarelli et al. Influence of photo-oxidation on the performance and soil degradation of oxo-and biodegradable polymer-based items for agricultural applications
KR102191338B1 (en) Eco-friendly composition improved in biodegradability and plasticity and the preparation method thereof
WO2018099223A1 (en) Biodegradable additive and plastic product added with same
US5505830A (en) Biodegradable compostable plastic and method of making the same
CN103865149A (en) Novel environment-friendly modified macromolecule material capable of triggering multiple-stage degradation and preparation method thereof
JPH04168150A (en) Biodegradable plastic
KR102196783B1 (en) Eco-friendly composition improved in heat-resistance and anti-hydrolysis and the preparation method thereof
US5667574A (en) Starch-based composition for preparing an environment degradable α-olefinic polymer molding material
CN103834084A (en) Environment-friendly modified high-polymer new material capable of initiating multiple degradation and preparation method thereof
KR102059294B1 (en) Eco-friendly composition biodegradable in natural condition and the preparation method thereof
KR20220059099A (en) Biodegradable resin compositions including polyvinylalcohol and manufacturing methods thereof
KR100800428B1 (en) Aerobic Biodegradable Container and Method for Producing it
WO2003050178A1 (en) Additive composition for promoting polymer degradation
KR100903885B1 (en) Aerobic biodegradable compound using poly lactic acid and method for producing it
KR100888090B1 (en) Biodegradable resin composition with improved durability
KR20210005339A (en) Biodegradable mulching film having the improved anti-hydrolysis property and manufacturing method thereof
Anna Dilfi et al. Linear Low Density Polyethylene-Biodegradability Using Bacteria from Marine Benthic Environment and Photodegradability Using Ultraviolet Light
KR100800429B1 (en) Aerobic Biodegradable Compound and Method for Producing it
KR20040016340A (en) Multi-degradable polypropylene composition and polypropylene product using the same
CN114163792A (en) Seawater degradable high-tension film packaging material and preparation method thereof

Legal Events

Date Code Title Description
E701 Decision to grant or registration of patent right
GRNT Written decision to grant