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Production technology of packaging composite film

A production process and composite film technology, which are applied in the directions of devices and coatings for coating liquid on the surface, can solve the problems of the barrier performance of the packaging composite film being difficult to meet the requirements of high-barrier drug packaging, and the complex preparation process of the packaging composite film. Achieve the effect of eliminating the corona step, shortening the working hours, and shortening the soaking time

Active Publication Date: 2019-01-18
SICHUAN HUILI IND
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] The purpose of the present invention is to provide a production process of packaging composite film to solve the problem that the existing packaging composite film preparation process is complicated, and the barrier performance of the packaging composite film prepared by the process is difficult to meet the requirements of high barrier drug packaging

Method used

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  • Production technology of packaging composite film

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0071] Preparation of hyperbranched cationic mussel-like polymer P1:

[0072]2,3,4-Trihydroxybenzoyl-isobenzoyl-(2-aminoethyl)acrylamide, N-(2-aminoethyl)(meth)acrylamide hydrochloride, 4-azide 2,3,5,6-tetrafluorobenzoylethylamine (meth)acrylamide, polyethylene glycol methyl ether acrylate (PEGMEA), polyethylene glycol diacrylate (PEGDEA, ethylene glycol The degree of polymerization is 22) and the RAFT reagent is added to the N,N-dimethylformamide solution with the concentration of 0.012M as the initiator 4,4'-azobis(4-cyanovaleric acid). Among them, the degree of polymerization of ethylene glycol in PEGMEA is 15, the degree of polymerization of ethylene glycol in PEGDEA is 22, 4,4'-azobis(4-cyanovaleric acid), RAFT reagent and all monomers involved in polymerization The molar ratio of the first reaction mixture is 1:2:100. 2,3,4-trihydroxybenzoyl-isobenzoyl-(2-aminoethyl)acrylamide:N-(2-aminoethyl) (Meth)acrylamide hydrochloride: 4-azido-2,3,5,6-tetrafluorophenacylethylamin...

Embodiment 2

[0079] Preparation of hyperbranched cationic mussel-like polymer P2:

[0080] 2,3,4-trihydroxybenzoyl p-benzamide ethyl (meth)acrylamide hydrochloride, N-(3-aminopropyl) (meth)acrylamide hydrochloride, 4- Nitro-2,3,5,6-tetrafluorobenzoylethylamine (meth)acrylamide, polyethylene glycol methyl ether acrylate (PEGMEA), polyethylene glycol diacrylate (PEGDEA) and RAFT The reagent is added to the N,N-dimethylformamide solution with the concentration of 0.012M of the initiator 2,2'-azobis(2-methylpropionitrile). Among them, the degree of polymerization of ethylene glycol in PEGMEA is 45, the degree of polymerization of ethylene glycol in PEGDEA is 10, 2,2'-azobis(2-methylpropionitrile), RAFT reagent and all monomers participating in polymerization The molar ratio of the first reaction mixture is 1:2:100. 2,3,4-trihydroxybenzoylbenzamide ethyl (meth)acrylamide hydrochloride: N-(3-aminopropyl) (Meth)acrylamide hydrochloride: 4-azido-2,3,5,6-tetrafluorophenacylethylamine (meth)acryla...

Embodiment 3

[0088] Preparation of hyperbranched cationic mussel-like polymer P3:

[0089] 2,3-Dihydroxybenzoylbenzoate amine ethyl (meth)acrylamide hydrochloride, N-(4-aminobutyl) (meth)acrylamide hydrochloride, 4-azide Base-phenacylethylamine (meth)acrylamide, polyethylene glycol methyl ether acrylate (PEGMEA), polyethylene glycol diacrylate (PEGDEA) and RAFT reagent 2-(dodecyltrithio Carbonate group)-2-methylpropionic acid was added to the N,N-dimethylformamide solution with a concentration of 0.012M of the initiator 2,2'-azobis(2-methylpropionitrile). Among them, the degree of polymerization of ethylene glycol in PEGMEA is 5, the degree of polymerization of ethylene glycol in PEGDEA is 8, 2,2'-azobis(2-methylpropionitrile), RAFT reagent and all monomers participating in polymerization The molar ratio of the first reaction mixture is 1:2:100. 2,3-Dihydroxybenzoylbenzoate amine ethyl(meth)acrylamide hydrochloride: N-(4-aminobutyl) (Meth)acrylamide hydrochloride: 4-azido-phenacylethylam...

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Abstract

The invention discloses a production technology of a packaging composite film. The technology comprises the following steps that 1, a hyperbranched cation mussel-inspired polymer is prepared to be anadhesive aqueous solution, wherein the hyperbranched cation mussel-inspired polymer comprises a polyo-phenolic hydroxyl methaqualone enamide monomer, a cationic monomer and an photoresponse monomer; 2, a graphene oxide solution is prepared; 3, a polymer thin film is soaked in the adhesive aqueous solution; 3, a polymer thin film is soaked in the adhesive aqueous solution, taken out, dried and thensoaked in the graphene oxide solution; 4, the polymer thin film prepared in step 3 is soaked in the adhesive water solution, taken out, dried and then soaked in the graphene oxide solution; 5, the step 4 is repeated; 6, a polymer thin film prepared in step 5 is put into an aqueous solution of a reducing agent, heating reflux condensation is conducted, and the packaging composite film is obtained.Accordingly, the corona step is omitted, not only is the technology cost lowered, but also the technology steps are simplified.

Description

technical field [0001] The invention relates to the field of packaging materials, in particular to a production process of a packaging composite film. Background technique [0002] As the main packaging material of pharmaceuticals, polymer film packaging materials have become more and more important in daily life. However, due to the influence of the plastic film production process and its own physical and chemical characteristics, it is difficult for the barrier properties of plastics to oxygen, water vapor, liquid substances and other low molecular weight substances to meet the requirements of most pharmaceutical packaging. The penetration of small molecular gases such as oxygen and water vapor into packaging materials will lead to oxidative deterioration of the active ingredients in the drug, which in turn will cause the reproduction of microorganisms and other phenomena. The direct consequence is that the shelf life of the drug is greatly shortened. Therefore, it is of ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B05D7/04C08J7/04C08J5/18C08F283/06C08F220/60C08L67/02
CPCC08F283/065C08J5/18B05D7/04C08F2438/03C08J2367/02C08J7/0423C08F220/603C08F220/606C08F220/60
Inventor 柏金枝张辉闫斌
Owner SICHUAN HUILI IND
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