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A kind of bulk chemical modification method of polymer

A chemical modification and polymer technology, applied in the field of polymers, can solve problems such as high cost and limited application prospects

Active Publication Date: 2020-11-13
CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although this type of method avoids the use of flammable and explosive organic peroxides, the method requires a higher initiator concentration (0.5 parts) and a higher chemical modification temperature (≥230 ° C), and the N-hydroxy compound The etherified and esterified compounds need to be prepared through complex synthetic processes, and the cost is much higher than that of organic peroxides, which greatly limits the application prospects of the above two methods
[0003] Another method involves high-energy ray irradiation pretreatment (Polymer 2006, 47, 1979), introducing macromolecular hydrogen peroxide and peroxide into the polymer molecular chain at room temperature, followed by Initiate monomer chemical modification reaction, this method can significantly improve the efficiency of chemical modification, but the cost is high

Method used

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  • A kind of bulk chemical modification method of polymer
  • A kind of bulk chemical modification method of polymer
  • A kind of bulk chemical modification method of polymer

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Experimental program
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preparation example Construction

[0057] In the present invention, there is no special limitation on the preparation sequence of the first masterbatch and the second masterbatch.

[0058] After the first masterbatch and the second masterbatch are obtained, the first masterbatch, the second masterbatch, the free radical polymerizable monomer and the polymer are mixed and heated for reaction to obtain the bulk chemically modified polymer.

[0059] Wherein, the molecular structure of the free radical polymerizable monomer contains a free radical polymerizable unsaturated double bond, preferably the monomer is glycidyl methacrylate, acrylic acid, methacrylic acid derivatives, acrylic acid derivatives, ethylene One or more of base siloxane, maleic anhydride, maleimide and maleimide derivatives; when the monomer contains a double bond, the polymer can be grafted Bulk modification; chemical crosslinking of polyolefins can be achieved when the monomers contain multiple double bonds. In special cases, when the monomer...

Embodiment 1~3

[0066] Fully mix 32g of high-density polyethylene powder (HDPE) and 0.64g of bis(pentafluorophenyl)methanone (BFBP) in an experimental high-speed mixer, and then add it to a 60cc torque rheometer produced by Shanghai Kechuang In the process, the preheating temperature of the torque rheometer is 175° C., the rotation speed is 30 rpm, and the carbonyl compound / HDPE masterbatch (2wt%) is obtained after fully mixing for 5 minutes.

[0067] N-hydroxy-2,2,6,6-tetramethylpiperidinol acetate (NHPA) / HDPE masterbatch (2wt%) was prepared by the same method as above, and the O-H fracture energy in NHPA molecule was 62kcal / mol.

[0068] The N-hydroxyoctylamide (NHO) / HDPE masterbatch (2wt%) was prepared by the same method as above, and the O-H fracture energy in the NHO molecule was 79kcal / mol.

[0069] The N-hydroxyl-2.3-pyridinedicarboximide (NHPI) / HDPE masterbatch (2wt%) was prepared by the same method as above, and the O-H fragmentation energy in the NHPI molecule was 89kcal / mol.

[00...

Embodiment 4~9

[0076] Adopt the method for implementation example 1 to prepare respectively benzophenone (BP) / HDPE (2wt%), diphenylsulfoxide (DPS) / HDPE (2wt%), p-trifluoromethyldiphenylsulfoxide (TFDPS) , benzoin dimethyl ether (BDE) / HDPE (2wt%), xanthone (XTO) / HDPE (2wt%) and cyclohexanone (CH) / HDPE (2wt%) masterbatch;

[0077] Mix 5 parts of the 6 carbonyl compound or sulfinyl compound masterbatches prepared above with 5 parts of N-hydroxyoctylamide (NHO) / HDPE masterbatch (2wt%), 2 parts of maleic anhydride (MAH) and 100 parts respectively The HDPE powder was added to a 60cc torque rheometer produced by Shanghai Kechuang. The torque rheometer was preheated at 200°C and the rotation speed was 50 rpm. After fully mixing for 5 minutes, MAH chemically modified HDPE was obtained.

[0078] The resulting MAH chemically modified HDPE was pressed into a 20 μm thick film, extracted with acetone for 36 hours to remove ungrafted MAH and N-hydroxyl compounds, and then vacuum-dried at 90°C overnight, an...

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Abstract

The invention provides a method for chemically modifying polymer bulk, comprising 0.05-1 mass parts of one of carbonyl compounds and sulfinyl compounds, 0.001-0.5 mass parts of hydroxyl compounds and 0.2-10 mass parts of free The monomers polymerized by the base are added to 100 parts by mass of the polymer melt, and mixed and reacted at the melting temperature to obtain the bulk chemically modified polymer. The graft modification method of polymer body provided by the invention has the characteristics of high process safety and low cost.

Description

technical field [0001] The invention belongs to the technical field of polymers, and in particular relates to a method for chemical modification of polymer bulk. Background technique [0002] Polymers are a class of materials with a wide range of uses, but for some applications, polymers must be chemically modified in bulk. An effective solution is to introduce polar grafts such as maleic anhydride (MAH), glycidyl methacrylate (GMA) and acrylic acid on the polymer molecular chain by free radical initiation. Organic peroxides are often added to polymer bulk chemical modification systems as free radical initiators to achieve the covalent bonding of polar monomers to polymer molecular chains. However, organic peroxides have many disadvantages. First, organic peroxides are regulated flammable and explosive products, and their use must strictly abide by national regulations; Many side reactions such as monomer self-polymerization, polymer degradation and cross-linking lead to l...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08F255/02C08F255/10C08F222/06C08F220/32C08F222/40C08F2/02
CPCC08F2/02C08F255/02C08F255/10C08F222/40C08F220/325
Inventor 杨华伟栾世方殷敬华石恒冲宋凌杰宋幼凌
Owner CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI