KR20030064950A - Mixed fog resistant composition for wrap employed in the packaging of food products - Google Patents
Mixed fog resistant composition for wrap employed in the packaging of food products Download PDFInfo
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- KR20030064950A KR20030064950A KR1020020005038A KR20020005038A KR20030064950A KR 20030064950 A KR20030064950 A KR 20030064950A KR 1020020005038 A KR1020020005038 A KR 1020020005038A KR 20020005038 A KR20020005038 A KR 20020005038A KR 20030064950 A KR20030064950 A KR 20030064950A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS 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
- B65D65/00—Wrappers or flexible covers; Packaging materials of special type or form
- B65D65/02—Wrappers or flexible covers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/16—Applications used for films
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
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Abstract
Description
본 발명은 식품 포장 랩용 복합 무적제 조성물에 관한 것이다.The present invention relates to a composite unfilled composition for food packaging wrap.
식품 포장에 사용되는 필름은 보통 연질 염화비닐, 저밀도 폴리에틸렌 등이다. 이들 필름의 표면은 소수성으로서 냉동식품, 채소류, 과일류 등을 포장시, 함유되어 있는 수분에 의해 필름의 표면에 물방울이 맺혀 흐려지게 된다. 이런 현상에 의해 제품의 외관이 나빠지거나 보관성이 좋지 않아 상품의 질을 떨어뜨린다.Films used for food packaging are usually soft vinyl chloride, low density polyethylene and the like. As the surface of these films is hydrophobic, when packaging frozen foods, vegetables, fruits, and the like, water droplets form on the surface of the film and become cloudy due to the moisture contained therein. Due to this phenomenon, the appearance of the product is deteriorated or the storage quality is poor, thereby degrading the quality of the product.
이러한 문제점을 해결하기 위하여 계면활성제를 필름에 넣거나 도포하여 필름 표면에 계면활성제의 층을 형성시킴으로써 임계 표면 장력을 크게 하여 친수성을 높이면 물방울은 깨어져 전체가 균일하게 젖어 빛의 투과가 좋아진다. 이렇게 이용되는 계면활성제를 무적제라 하며, 식품 포장 랩에서 무적제의 배합은 필수적이다.In order to solve this problem, by adding or applying a surfactant to the film to form a layer of the surfactant on the surface of the film to increase the critical surface tension to increase the hydrophilicity, the water droplets are broken and the whole is uniformly wet to improve the light transmission. The surfactants used in this way are called invincibles, and the formulation of the invincible is essential in food packaging wraps.
무적제를 합성수지에 배합하여 넣을 때 가공 온도가 높으므로 열안정성이 좋지 않으면 필름 투명도가 저하되거나 변색하게 된다. 또한 무적제의 과도한 브리드에 의한 접착성에 의해 필름의 풀림성이 좋지 않아 사용상 불편을 느끼기도 하며,식품 포장시 접착력이 없어 포장 재료로서의 효율이 떨어지는 등의 문제점이 있다.When the formulation is added to the synthetic resin, the processing temperature is high, so if the thermal stability is not good, the film transparency will be degraded or discolored. In addition, due to the adhesiveness due to excessive bleeding of the unfilled agent, the unwinding property of the film is not good, there is also a inconvenience in use, there is a problem such as poor efficiency as a packaging material because there is no adhesive force during food packaging.
이에, 본 발명자는 이와 같은 문제점을 해결하기 위하여 식품 포장용 필름에 배합하는 무적제의 효과를 극대화하도록 무적제를 개량하여 본 발명을 완성하였다.Thus, the present inventors have completed the present invention by improving the non-additives to maximize the effect of the additives in the film for food packaging in order to solve such problems.
본 발명자는 식품 포장 랩의 무적성과 열안정성이 우수한 무적제를 만들기 위해 연구를 진행하던 중 고급지방산-다가 알콜 에스테르가 효과가 큰 것을 발견하여 본 발명에 이르게 되었다.The present inventors found that higher fatty acid-polyhydric alcohol esters had a great effect during the study to make an invincible agent having excellent invincibility and thermal stability of food packaging wraps, and thus led to the present invention.
본 발명은 식품 포장 랩에 탁월한 무적 효과를 제공하는, 즉 수지와의 상용성, 초기 무적성, 랩의 풀림성 및 접착성 등의 복합 무적 효과를 나타내는 식품 포장 랩용 복합 무적제 조성물을 제공하기 위한 것이다.The present invention is to provide a composite invincible composition for food packaging wraps that provides an excellent invincible effect on food packaging wraps, that is, a composite invincible effect such as compatibility with the resin, initial invincibility, unwinding and adhesion of the wrap .
본 발명은 다가 알콜:탄소수 10 내지 20의 고급 지방산을 1.0:1.0 내지 1.0:2.0의 몰중량비로 에스테르 반응시켜 얻어지는 반응 생성물(A), 글리세린:올레인산을 1.0:1.0 내지 1.0:2.0의 몰중량비로 에스테르 반응시켜 얻어지는 반응 생성물(B) 및 고급 알콜:산화에틸렌을 1:1 내지 1:7의 몰중량비로 부가 반응시켜 얻어지는 부가 반응 생성물(C)을 70:20:10 내지 30:20:50의 중량비로 혼합하여 제조한 식품 포장 랩용 복합 무적제 조성물을 제공한다.The present invention provides a reaction product (A) obtained by esterifying a polyhydric alcohol: a higher fatty acid having 10 to 20 carbon atoms in a molar weight ratio of 1.0: 1.0 to 1.0: 2.0, and a glycerin: oleic acid in a molar weight ratio of 1.0: 1.0 to 1.0: 2.0. The reaction product (B) obtained by esterification and the addition reaction product (C) obtained by addition-reacting the higher alcohol: ethylene oxide in the molar weight ratio of 1: 1-1: 7 are 70: 20: 10-30: 20: 50 It provides a composite unpacking composition for food packaging wraps prepared by mixing in a weight ratio.
식품 포장 랩의 경우 농업용 비닐하우스처럼 응축된 물로 필름 표면이 계속 씻기는 경우가 없으므로 무적성의 장기 지속성은 그다지 문제가 되지 않으며 우수한 초기 무적성이 요구된다.In food packaging wraps, the film surface is never washed with condensed water like agricultural greenhouses, so long-term persistence of invincibility is not a problem and requires good initial invincibility.
본 발명에 사용된 고급지방산은 탄소수 10-20의 지방산으로, 예를 들면 라우린산, 미리스트산, 팔미틴산, 스테아린산, 리놀렌산, 리놀레산, 아라키돈산 등이 있다. 특히, 탄소수 12-14 범위의 지방산인 라우린산과 미리스트산이 보다 효과적이다. 다가 알콜로는 예를 들어 솔비톨, 글리세린, 디글리세린, 폴리글리세린 등을 포함한다. 에스테르 합성시 다가알콜/고급지방산의 몰 비율은 1.0/1.0 내지 1.0/2.0의 범위가 적당하나, 1.0/1.3 내지 1.0/1.5의 범위가 효과가 뛰어났다.The higher fatty acids used in the present invention are fatty acids having 10 to 20 carbon atoms, for example, lauric acid, myristic acid, palmitic acid, stearic acid, linolenic acid, linoleic acid, arachidonic acid and the like. In particular, lauric acid and myristic acid, which are fatty acids in the range of 12-14 carbon atoms, are more effective. Polyhydric alcohols include, for example, sorbitol, glycerin, diglycerine, polyglycerine and the like. The molar ratio of polyhydric alcohol / high fatty acid in the synthesis of ester is suitably in the range of 1.0 / 1.0 to 1.0 / 2.0, but the range of 1.0 / 1.3 to 1.0 / 1.5 was excellent.
식품 포장 랩의 풀림성을 개선하기 위해 글리세린-올레인산 에스테르를 사용하였으며 글리세린/올레인산의 몰 비율은 1.0/1.0 내지 1.0/2.0의 범위가 적당하나 1.0/1.3 내지 1.0/1.5의 범위가 효과가 뛰어났다.Glycerin-oleic acid ester was used to improve the unwindability of food packaging wraps. The molar ratio of glycerin / oleic acid was in the range of 1.0 / 1.0 to 1.0 / 2.0, but the range of 1.0 / 1.3 to 1.0 / 1.5 was effective. .
랩의 접착성을 좋게 하기 위하여 고급 알콜-산화에틸렌 부가물을 사용하였다. 여기에 사용된 고급 알콜로는 탄소수 12 내지 18 범위가 적당하나, 탄소수 12 내지 16의 범위가 효과가 뛰어났다. 고급 알콜-산화에틸렌의 몰 비율은 1.0/1.0 내지 1.0/10.0의 범위가 적당하나 1.0/3.0 내지 1.0/7.0의 범위가 효과가 뛰어났다.Higher alcohol-ethylene oxide adducts were used to improve the adhesion of the wraps. The higher alcohol used herein is preferably in the range of 12 to 18 carbon atoms, but the range of 12 to 16 carbon atoms is excellent. The molar ratio of the higher alcohol-ethylene oxide is suitably in the range of 1.0 / 1.0 to 1.0 / 10.0, but the range of 1.0 / 3.0 to 1.0 / 7.0 was excellent.
따라서, 식품 포장 랩의 초기무적성, 풀림성 및 접착성을 동시에 제공하기 위하여, 상기 다가 알콜-고급 지방산 에스테르, 글리세린/올레인산 에스테르, 고급 알콜-산화에틸렌 부가물을 혼합 사용한 결과 상기 모든 성능면에서 우수한 효과를 나타내어 종래 기술의 문제점을 해결할 수 있었다. 이 때, 혼합 비율은 70:20:10 내지 30:20:50의 범위가 적당하나, 특히 30:20:50의 비율이 효과적이었다.Therefore, in order to simultaneously provide the initial unsatisfaction, slackness and adhesiveness of the food packaging wrap, the result of using the polyhydric alcohol-high fatty acid ester, glycerin / oleic acid ester, higher alcohol-ethylene oxide adduct as a result of all the above performance By showing an excellent effect it was possible to solve the problems of the prior art. At this time, the mixing ratio was suitably in the range of 70:20:10 to 30:20:50, and particularly, the ratio of 30:20:50 was effective.
다가 알콜과 고급 지방산의 에스테르 반응은 당해 기술 분야에 잘 알려진 조건하에서 실시할 수 있다. 구체적으로, 질소하에 촉매로서 가성소다를 0.3% 내지0.5% 첨가하고, 170 내지 250℃의 온도에서 5 내지 7시간 동안 반응하여 에스테르 반응생성물을 얻을 수 있다.The ester reaction of polyhydric alcohols with higher fatty acids can be carried out under conditions well known in the art. Specifically, 0.3% to 0.5% of caustic soda can be added as a catalyst under nitrogen, and reacted at a temperature of 170 to 250 ° C. for 5 to 7 hours to obtain an ester reaction product.
글리세린과 올레인산의 에스테르 역시 전술한 에스테르 반응 조건하에 1:1.5의 몰중량비를 투입하여 수득할 수 있다.Esters of glycerin and oleic acid can also be obtained by introducing a molar weight ratio of 1: 1.5 under the above-described ester reaction conditions.
고급 알콜-산화에틸렌의 부가 반응은 각 반응물을 오토클레이브에 넣고 150 내지 180℃에서 3 내지 5㎏/㎠ 의 조건으로 3 내지 5시간 동안 실시하면 본 발명의 부가 생성물을 얻을 수 있다.The addition reaction of the higher alcohol-ethylene oxide may be carried out by placing each reactant in an autoclave for 3 to 5 hours at a temperature of 3 to 5 kg / cm 2 at 150 to 180 ° C. to obtain the addition product of the present invention.
본 발명의 복합 무적제를 사용하여 목적하는 복합 무적 효과를 나타내는 식품 포장 랩 필름을 제조할 수 있다. 이와 같은 랩 필름은 예를 들어 연질염화비닐과 본 발명의 무적제 및 기타 에폭시화대두유, 가소제, 안정제를 반바리 믹서 중에서 용융 배합한 뒤, 인프레션 가공 장치를 통해 통과시켜 제조할 수 있다. 얻어지는 랩 필름은 하기 실시예에 제시된 무적 효과를 관찰 평가하기 위한 시험을 통해 효과를 확인할 수 있다.The composite unpacking agent of the present invention can be used to produce a food packaging wrap film that exhibits the desired composite unloading effect. Such a wrap film can be produced, for example, by melt-blending a soft vinyl chloride, the invincible agent of the present invention, and other epoxidized soybean oils, plasticizers, and stabilizers in a half-barrier mixer, and then passing them through an impression processing apparatus. The resulting wrap film can be verified by a test for observing and evaluating the invincible effects shown in the Examples below.
하기 실시예에 따라 본 발명의 효과를 구체적으로 설명하면 다음과 같으며 본 발명은 실시예에 한정되는 것은 아니다.When explaining the effects of the present invention in detail according to the following examples, the present invention is not limited to the examples.
실시예 1Example 1
고급지방산-다가 알콜 에스테르의 제조예 1Preparation Example 1 of higher fatty acid-polyhydric alcohol ester
4구 플라스크에 솔비톨과 라우린산을 1:1.3의 몰중량비로 넣고 촉매로서 가성소다 0.4%를 첨가하며, 냉각 콘덴사를 부착하고 질소를 투입하면서 240-250℃의 조건하에서 5시간 반응하여 에스테르 반응물을 얻었다.In a four-necked flask, sorbitol and lauric acid were added in a molar weight ratio of 1: 1.3, and caustic soda 0.4% was added as a catalyst.The reaction was carried out under 240-250 ° C. for 5 hours while attaching cooling condensate and nitrogen. The reaction was obtained.
실시예 2Example 2
고급지방산-다가 알콜 에스테르의 제조예 2Preparation Example 2 of higher fatty acid-polyhydric alcohol ester
실시예 1에서 솔비톨과 라우린산 대신에 글리세린과 팔미틴산을 1:1.5의 몰중량비로 투입하고 반응 온도 170-180℃의 조건으로 반응한 외에는 실시예 1과 같이 실시하여 에스테르 반응 생성물을 얻었다.In Example 1, instead of sorbitol and lauric acid, glycerin and palmitic acid were added at a molar weight ratio of 1: 1.5, and the reaction was carried out in the same manner as in Example 1 except that the reaction was carried out under the conditions of a reaction temperature of 170-180 ° C to obtain an ester reaction product.
실시예 3Example 3
고급지방산-다가 알콜 에스테르의 제조예 3Preparation Example 3 of higher fatty acid-polyhydric alcohol ester
실시예 2에서 글리세린과 팔미틴산 대신에 디글리세린과 라우린산을 1:1.5의 몰중량비로 투입한 외는 실시예 2와 같이 실시하여 에스테르 반응 생성물을 얻었다.Diglycerin and lauric acid were added in a molar weight ratio of 1: 1.5 instead of glycerin and palmitic acid in Example 2, and the reaction was carried out as in Example 2 to obtain an ester reaction product.
실시예 4Example 4
글리세린-올레인산 에스테르의 제조Preparation of Glycerine-Oleic Acid Ester
실시예 2에서 글리세린과 팔미틴산 대신에 글리세린과 올레인산을 1:1.3의 몰중량비로 투입한 외는 실시예 2와 같이 실시하여 에스테르 반응 생성물을 얻었다.In Example 2, except that glycerin and oleic acid were added at a molar weight ratio of 1: 1.3 instead of glycerin and palmitic acid, it was carried out as in Example 2 to obtain an ester reaction product.
실시예 5Example 5
고급 알콜-산화에틸렌 부가물의 제조Preparation of Higher Alcohol-Ethylene Oxide Additives
오토클레이브에 라우릴알콜과 산화에틸렌을 1:3의 몰중량비로 투입하고 150℃, 4㎏/㎠의 조건으로 5시간 부가 반응시켜 부가 반응 생성물을 얻었다.Lauryl alcohol and ethylene oxide were added to the autoclave at a molar weight ratio of 1: 3, and addition reaction was carried out at 150 ° C and 4 kg / cm 2 for 5 hours to obtain an addition reaction product.
실시예 6Example 6
실시예 1 : 실시예 4 : 실시예 5의 반응 생성물을 중량비 70:20:10의 비율로 혼합하여 혼합물을 얻었다.Example 1 Example 4 The reaction product of Example 5 was mixed at a weight ratio of 70:20:10 to obtain a mixture.
실시예 7Example 7
실시예 2 : 실시예 4 : 실시예 5의 반응 생성물을 중량비 40:20:40의 비율로 혼합하여 혼합물을 얻었다.Example 2 Example 4 The reaction product of Example 5 was mixed in a weight ratio of 40:20:40 to obtain a mixture.
실시예 8Example 8
실시예 3 : 실시예 4 : 실시예 5의 반응물을 중량비 30:20:50의 비율로 혼합하여 혼합물을 얻었다.Example 3 Example 4 The reactants of Example 5 were mixed in a weight ratio of 30:20:50 to obtain a mixture.
실시예 9Example 9
연질 염화비닐 수지와 실시예 1 - 8의 무적제를 사용하여 시험용 ??을 제조하였으며 배합량과 가공조건은 다음과 같다.Test ?? was prepared using a soft vinyl chloride resin and the invincible agent of Examples 1-8, and the blending amount and processing conditions are as follows.
1) 배합량1) Compounding amount
사용수지연질염화비닐100Resin Soft Vinyl Chloride 100
첨가물에폭시화대두유10PHRAdditive Epoxylated Soybean Oil 10PHR
가소제(DOP)40PHRPlasticizer (DOP) 40 PHR
안정제0.5PHRStabilizer 0.5PHR
무적제2.5PHRInvincible 2.5PHR
2) 가공 조건2) processing conditions
1. 혼합반바리 믹서에 의한 용융 배합1. Melt blending by mixing bandi mixer
2. 가공 장치인프레션 가공장치2. Induction Processing Equipment
압출기스크류 D=40㎜ L/D=24 C.R=4.2Extruder Screw D = 40mm L / D = 24 C.R = 4.2
40rpm스프릿 8m/min. B.U.R=1.540 rpm Split 8 m / min. B.U.R = 1.5
다이스피이랄 Type D=75㎜ 스릿트=0.5㎜Die spiral type D = 75mm split = 0.5mm
냉각공냉Cooling
필름의 두께0.06㎜Thickness of film 0.06mm
실시예 10Example 10
시험용 랩을 사용하여 다음과 같이 무적성 효과를 비교하였으며 그 결과는 표 1과 같다A test lab was used to compare invincibility effects as follows, and the results are shown in Table 1.
<무적성 시험 방법><Invincibility test method>
용량 500㎖의 비커에 90℃의 온수를 400㎖ 넣고 시료 필름으로 밀폐한 후 방치하여 필름 내부의 무적 효과를 관찰, 평가한다.400 ml of hot water at 90 ° C. was placed in a 500 ml beaker, sealed with a sample film, and left to stand to observe and evaluate the invincible effect inside the film.
비교예 1Comparative Example 1
글리세린-모노스테아레이트를 실시예 9의 방법으로 필름을 제조하고 실시예 10의 방법으로 시험한 결과는 표 1과 같다.Glycerin-monostearate was prepared by the method of Example 9 to the film and the results of the test of the method of Example 10 are shown in Table 1.
비교예 2Comparative Example 2
비교예 1의 글리세린-모노스테아레이트 대신에 솔비탄-모노스테아레이트를 사용한 외는 비교예 1과 같다.The use of sorbitan-monostearate in place of the glycerin-monostearate of Comparative Example 1 was the same as in Comparative Example 1.
비교예 3Comparative Example 3
비교예 1의 글리세린-모노스테아레이트 대신에 솔비탄-모노올레이트를 사용한 외는 비교예 1과 같다.The use of sorbitan monooleate in place of the glycerin monostearate of Comparative Example 1 was the same as in Comparative Example 1.
평가기준Evaluation standard
1) 무적성A: 물방울이 전혀 보이지 않는 상태1) Invincible A: No water droplets
B: 약간의 물방울이 부착되어 있는 상태(거의 투명)B: Some water droplets are attached (almost transparent)
C: 물방울의 부착이 약 30% 내지 50%인 상태C: adhesion of water droplets is about 30% to 50%
D: 전면에 걸쳐 물방울이 부착된 상태D: Water droplets attached to the front
2) 풀림성○ : 풀림성이 양호한 상태2) Unwinding ○: Unwinding
△ : 풀림성이 중간△: loosening property is medium
× : 풀림성이 불량×: loosening property is poor
3) 접착성○ : 접착성 양호3) Adhesive ○: Good adhesive
△ : 접착성 중간△: adhesive intermediate
× : 접착성 불량×: poor adhesion
상기 표 1을 통해 알 수 있듯이, 실시예 1 내지 5의 무적제를 단독으로 사용한 경우보다 실시예 6 내지 8에서와 같이 본 발명에 개시된 3종의 무적제를 일정비율로 혼합한 혼합물을 단품으로 사용했을 때 무적성, 풀림성 및 접착성 면에서 모두 뛰어난 무적 효과가 나타난다는 것을 확인할 수 있었다.As can be seen from the above Table 1, as in Examples 6 to 8 as compared to the case of using the invincible agents of Examples 1 to 5 alone, a mixture of three kinds of invincible agents disclosed in the present invention at a constant ratio was used separately. At the time of the invincibility, unwinding and adhesiveness it was confirmed that the excellent invincible effect appears.
이상 설명드린 본 발명의 복합 무적제는 3종의 무적제를 일정 비율로 혼합하여 단품화한 무적제 조성물로서, 식품 포장 ??에 요구되는 무적성, 풀림성 및 접착성을 동시에 제공하여 성능면에서 뛰어나 포장 재료로서 경제적 이용가치가 클 것으로 사료된다.As described above, the composite unseparable agent is a undivided composition obtained by mixing three kinds of unsecured agents in a certain ratio, and provides excellent performance in terms of performance by simultaneously providing unsatisfactory, unsealable, and adhesive properties required for food packaging. It is considered to be of great economic value as a material.
Claims (7)
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60229951A (en) * | 1984-04-27 | 1985-11-15 | Mitsubishi Kasei Vinyl Co | Antifogging synthetic resin film |
KR890014640A (en) * | 1988-03-18 | 1989-10-25 | 로버트 프랭크 노르토버 | Food Packaging Film |
JPH11335486A (en) * | 1998-05-27 | 1999-12-07 | Kao Corp | Antifog composition for synthetic resin |
JP2001164056A (en) * | 1999-12-07 | 2001-06-19 | Sekisui Chem Co Ltd | Polyolefin-based resin film |
-
2002
- 2002-01-29 KR KR1020020005038A patent/KR20030064950A/en not_active Application Discontinuation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60229951A (en) * | 1984-04-27 | 1985-11-15 | Mitsubishi Kasei Vinyl Co | Antifogging synthetic resin film |
KR890014640A (en) * | 1988-03-18 | 1989-10-25 | 로버트 프랭크 노르토버 | Food Packaging Film |
JPH11335486A (en) * | 1998-05-27 | 1999-12-07 | Kao Corp | Antifog composition for synthetic resin |
JP2001164056A (en) * | 1999-12-07 | 2001-06-19 | Sekisui Chem Co Ltd | Polyolefin-based resin film |
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