KR970070105A - Polyamide resin composition for producing a film - Google Patents

Polyamide resin composition for producing a film Download PDF

Info

Publication number
KR970070105A
KR970070105A KR1019960010523A KR19960010523A KR970070105A KR 970070105 A KR970070105 A KR 970070105A KR 1019960010523 A KR1019960010523 A KR 1019960010523A KR 19960010523 A KR19960010523 A KR 19960010523A KR 970070105 A KR970070105 A KR 970070105A
Authority
KR
South Korea
Prior art keywords
carbon atoms
alkyl group
integer
acid ester
following formula
Prior art date
Application number
KR1019960010523A
Other languages
Korean (ko)
Other versions
KR100200046B1 (en
Inventor
박명수
오명환
하승민
서양석
Original Assignee
백영배
동양나이론 주식회사
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 백영배, 동양나이론 주식회사 filed Critical 백영배
Priority to KR1019960010523A priority Critical patent/KR100200046B1/en
Publication of KR970070105A publication Critical patent/KR970070105A/en
Application granted granted Critical
Publication of KR100200046B1 publication Critical patent/KR100200046B1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/02Polyamides derived from omega-amino carboxylic acids or from lactams thereof
    • 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
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • 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
    • C08K3/01Use of inorganic substances as compounding ingredients characterized by their specific function
    • C08K3/013Fillers, pigments or reinforcing additives
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/24Acids; Salts thereof
    • C08K3/26Carbonates; Bicarbonates
    • 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
    • C08K3/34Silicon-containing 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
    • C08K3/34Silicon-containing compounds
    • C08K3/36Silica
    • 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
    • C08K5/103Esters; Ether-esters of monocarboxylic acids with polyalcohols
    • 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
    • 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
    • C08K3/24Acids; Salts thereof
    • C08K3/26Carbonates; Bicarbonates
    • C08K2003/265Calcium, strontium or barium carbonate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/28Non-macromolecular organic substances
    • C08L2666/40Phosphorus-containing compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/28Non-macromolecular organic substances
    • C08L2666/52Metal-containing compounds

Abstract

본 발명은 나이론 6을 주성분으로 한 공중합물 100중량%에 대해 평균입경이 0.1∼6㎛, 표면적이 300m2/g 이상인 무기미립자가 0.03∼0.12중량%, 하기 구조식(I), (Ⅱ)로 표시되는 6환과 5환으로 이루어진 폴리옥시에틸렌솔비탄지방산에스터와 하기 식(Ⅲ)의 글리세린모노지방산에스터를 30∼50/30∼50/0∼40의 중량비로 혼합한 비이온성 에스터계 계면활성제 0.01∼0.5중량%, 하기 식(Ⅳ)의 인산에스터염 또는 하기 식(Ⅴ)의 인산에스터가 0.001∼5중량%를 포함하는 것을 특징으로 하는 필름제조용 폴리아미드수지 조성물을 제공하는 것으로, 본 발명의 조성물에 의해 제조되는 필름은 표면특성, 투명성, 대전방지성이 우수하고 수요자의 요구에 적합하도록 제조될 수 있는 잇점을 갖는다.The present invention relates to a process for producing a nylon 6-containing copolymer, comprising the steps of: (1) preparing a copolymer comprising 100% by weight of a copolymer comprising nylon 6 as a main component and 0.03 to 0.12% by weight of an inorganic fine particle having an average particle size of 0.1 to 6 μm and a surface area of 300 m 2 / A nonionic ester surfactant 0.01 in which a polyoxyethylene sorbitan fatty acid ester consisting of six rings and five rings shown and a glycerin mono fatty acid ester represented by the following formula (III) were mixed at a weight ratio of 30/50/30 to 50/0/40 To 0.5% by weight of a phosphoric acid ester salt of the following formula (IV) or 0.001 to 5% by weight of a phosphoric acid ester of the following formula (V). The film produced by the composition has an advantage of being excellent in surface characteristics, transparency, antistatic property and being manufactured to meet the requirements of the consumer.

(상기 식에서, R은 탄소수 5∼20의 알킬기, n1, n2,n3은 각각 5∼20의 정수이다.)(Wherein R is an alkyl group having 5 to 20 carbon atoms, n 1 , n 2 and n 3 are each an integer of 5 to 20)

(상기 식에서, R은 탄소수 5∼20의 알킬기, n1, n2,n3은 각각 5∼20의 정수이다.)(Wherein R is an alkyl group having 5 to 20 carbon atoms, n 1 , n 2 and n 3 are each an integer of 5 to 20)

(상기 식에서, R은 탄소수 2∼20의 알킬기이다.)(Wherein R is an alkyl group having 2 to 20 carbon atoms)

(상기 식에서, R은 탄소수 2∼20의 알킬기, n1, n2는 각각 2∼20의 정수, M+는 Na+또는 K+이다.)(Wherein R is an alkyl group having 2 to 20 carbon atoms, n 1 and n 2 are each an integer of 2 to 20, and M + is Na + or K + .)

(상기 식에서, R은 탄소수 2∼20의 알킬기, n1, n2는 각각 2∼20의 정수이다.)(Wherein R is an alkyl group having 2 to 20 carbon atoms, n 1 and n 2 each are an integer of 2 to 20)

Description

필름제조용 폴리아미드수지 조성물Polyamide resin composition for producing a film

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is a trivial issue, I did not include the contents of the text.

Claims (3)

나이론 6을 주성분으로 한 공중합물 100중량%에 대해 평균입경이 0.1∼6㎛, 표면적이 300m2/g이상인 무기미립자가 0.03∼0.12중량%, 하기 구조식(I),(Ⅱ)로 표시되는 6환과 5환으로 이루어진 폴리옥시에틸렌솔비탄지방산에스터와 하기 식(Ⅲ)의 글리세린모노지방산에스터를 30∼50/30∼50/0∼40의 중량비로 혼합한 비이온성 에스터계 계면활성제 0.01∼0.5중량%, 하기 식(Ⅳ)의 인산에스터염 또는 하기 식(Ⅴ)의 인산에스터가 0.001∼5중량%를 포함하며, 상대점도 3.3~3.8, 분자량분포 2~4범위이며, 열수추출분이 0.5% 이하인 것을 특징으로 하는 필름제조용 폴리아미드수지 조성물.(I) and 6 (II) represented by the following structural formulas (I) and (II), wherein the inorganic fine particles having an average particle size of 0.1 to 6 μm and a surface area of 300 m 2 / g or more are contained in an amount of 0.03 to 0.12% 0.01 to 0.5 wt.% Of a nonionic ester surfactant obtained by mixing a polyoxyethylene sorbitan fatty acid ester composed of a ring and five rings with a glycerin mono fatty acid ester of the following formula (III) in a weight ratio of 30/50/30 to 50/0 to 40 %, A phosphoric acid ester salt of the following formula (IV) or a phosphate ester of the following formula (V) in an amount of 0.001 to 5 wt%, a relative viscosity of 3.3 to 3.8, a molecular weight distribution of 2 to 4, ≪ / RTI > (상기 식에서, R은 탄소수 5∼20의 알킬기, n1, n2,n3은 각각 5∼20의 정수이다.)(Wherein R is an alkyl group having 5 to 20 carbon atoms, n 1 , n 2 and n 3 are each an integer of 5 to 20) (상기 식에서, R은 탄소수 5∼20의 알킬기, n1, n2,n3은 각각 5∼20의 정수이다.)(Wherein R is an alkyl group having 5 to 20 carbon atoms, n 1 , n 2 and n 3 are each an integer of 5 to 20) (상기 식에서, R은 탄소수 2∼20의 알킬기이다.)(Wherein R is an alkyl group having 2 to 20 carbon atoms) (상기 식에서, R은 탄소수 2∼20의 알킬기, n1, n2는 각각 2∼20의 정수, M+는 Na+또는 K+이다.)(Wherein R is an alkyl group having 2 to 20 carbon atoms, n 1 and n 2 are each an integer of 2 to 20, and M + is Na + or K + .) (상기 식에서, R은 탄소수 2∼20의 알킬기, n1, n2는 각각 2∼20의 정수이다.)(Wherein R is an alkyl group having 2 to 20 carbon atoms, n 1 and n 2 each are an integer of 2 to 20) 제1항에 있어서, 상기 나이론 6을 주성분으로 한 공중합물인 a)카프로락탐 95-99.9중량%와 b)헥사메틸렌디아민, 2-메틸펜타메틸렌디아민, 메타파라크실렌디아민, 아디프산, 12-아미노도데칸산 또는 라우릴락탐으로 구성되는 군으로부터 선택되는 1종 이상의 혼합물을 0.01-5중량%을 용융중합하여 제조되는 것을 특징으로 하는 필름제조용 폴리아미드수지 조성물.The composition according to claim 1, which comprises a copolymer comprising 95 to 99.9% by weight of caprolactam, which is a copolymer mainly composed of nylon 6, and b) hexamethylenediamine, 2-methylpentamethylenediamine, metaparaxylenediamine, adipic acid, Wherein the polyamide resin composition is prepared by melt blending 0.01 to 5 wt% of at least one selected from the group consisting of dodecanoic acid and lauryllactam. 제1항에 있어서, 상기 무기미립자가 실리카, 카올린, 탈크, 탄산칼슘, 알루미나 또는 이들의 2종 이상의 혼합물로 구성되는 군으로부터 선택되는 것을 특징으로 하는 필름제조용 폴리아미드수지 조성물.The polyamide resin composition for producing a film according to claim 1, wherein the inorganic fine particles are selected from the group consisting of silica, kaolin, talc, calcium carbonate, alumina or a mixture of two or more thereof. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: It is disclosed by the contents of the first application.
KR1019960010523A 1996-04-08 1996-04-08 Polyamide resin composition KR100200046B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1019960010523A KR100200046B1 (en) 1996-04-08 1996-04-08 Polyamide resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1019960010523A KR100200046B1 (en) 1996-04-08 1996-04-08 Polyamide resin composition

Publications (2)

Publication Number Publication Date
KR970070105A true KR970070105A (en) 1997-11-07
KR100200046B1 KR100200046B1 (en) 1999-06-15

Family

ID=19455286

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019960010523A KR100200046B1 (en) 1996-04-08 1996-04-08 Polyamide resin composition

Country Status (1)

Country Link
KR (1) KR100200046B1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100604739B1 (en) * 2002-11-26 2006-07-26 주식회사 효성 High-shrink 3-dimension polyamide polymer and polyamide fiber thereby

Also Published As

Publication number Publication date
KR100200046B1 (en) 1999-06-15

Similar Documents

Publication Publication Date Title
TW324732B (en) Biodegradable polymers, the preparation thereof and the use thereof for the production of biodegradable moldings the invention relates to a biodegradable polyetheresteramide, which is produced by reacting a mixture comprising a polyetheresteramide P1, vinyl ether and a compound D.
TW324731B (en) Biodegradable polymers, the preparation thereof and the use thereof for the production of biodegradable moldings
US4767741A (en) Two-phase liquid cosmetic and method of preparing same
US5498280A (en) Phosphorescent and fluorescent marking composition
US4518727A (en) Water based resin emulsions
BR9713799A (en) Composition, molded article, and process for preparing a high i.v.
NZ305268A (en) Detergent cleaning composition comprising diacyl peroxide particulates, and preparation thereof
KR910003078A (en) Lubricant composition
DE69832720D1 (en) PARTICLES COMPRISING A STABILIZED FREE RADICAL, POLYMERIZED MODIFIED PARTICLES AND METHOD OF PRODUCTION THEREOF
GB2305922A (en) Polyamide resin composition
US4187192A (en) Talc dispersions
DK164458C (en) APPLICATION OF POWDER-DEFINED COATING MATERIALS BASED ON POLYAMIDS WITH AVERAGE AT LEAST 9 CARBON ATOMS PER. CARBONAMIDE GROUP AS COATING AGENT BY MELT-COATING METHOD
KR960703661A (en) Concentrated aqueous compositions of alkylpolyglycosides and uses thereof
CA1198026A (en) Stable liquid detergent suspensions
KR970070105A (en) Polyamide resin composition for producing a film
DE69838621D1 (en) PROCESS FOR PREPARING NANOCOMPOSITE COMPOSITIONS
CA2082744A1 (en) Moulding compositions containing a polycondensation product
EP0737719A3 (en) Thermoplastic compositions based on partial aromatic polyamides and polyetherimides
FI76359C (en) Polyamide films and their preparation process
KR970705414A (en) The present invention relates to a cholesterol ester covering agent, a cholesterol ester covering agent, a repair composition, a catcher composition, a cosmetic composition containing the same,
KR970070103A (en) Polyamide resin composition for film
KR930021717A (en) How to prepare a polyester container
KR940009316A (en) Liquid crystalline resin composition
KR970706346A (en) Polyolefins with permanent antistatic and anti-fogging properties, processes for their preparation and their uses
KR930006194A (en) Manufacturing method of polyester monofilament for zipper

Legal Events

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

Payment date: 20121220

Year of fee payment: 15

FPAY Annual fee payment

Payment date: 20140206

Year of fee payment: 16

FPAY Annual fee payment

Payment date: 20150205

Year of fee payment: 17

EXPY Expiration of term