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A kind of urethane-organic silicon-acrylic ester ternary copolymerization emulsion and preparation method thereof

A technology of acrylate ternary and copolymerized emulsion, which is applied in dyeing, textiles and papermaking, etc. It can solve the problems of poor fabric softness and low rubbing fastness, and achieve soft hand feeling, good dry/wet rubbing fastness, good The effect of crosslinking properties

Active Publication Date: 2016-08-24
深圳天鼎新材料有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] In view of the above-mentioned deficiencies in the prior art, the object of the present invention is to provide a urethane-organic silicon-acrylate ternary copolymerization emulsion and a preparation method thereof, aiming at solving the problem of the low rubbing fastness of the current pigment printing adhesive, the The problem of poor fabric softness after finishing

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0052] Embodiment 1 (component content uses parts by weight in all embodiments, and the unit is gram)

[0053] 1. Preparation of reactive urethane-silicon-acrylate polymer

[0054] Add 32g of polyether siloxane diol IM22 and 10g of polyether diol (N210) into a four-necked flask equipped with a stirrer and reflux condenser, at 100-110°C, the vacuum degree is 0.098 Vacuum dehydration for 2 hours, and then cooling to 40°C, add 30g 2,4-toluene diisocyanate (TDI), 4.5g 2,2-dimethylol propionic acid, 30g butanone, 1.2g 1,4 butanedi Alcohol, then heat up to 85°C, react at a constant temperature for 3 hours, cool to 60°C after the reaction, add 15g of hydroxyethyl methacrylate for capping, complete the dropwise addition in 0.5 hours, then react at a constant temperature for 2 hours, cool down after the reaction To 45°C, add 3g triethylamine to react for 10 minutes, then add 254g deionized water and 0.8g ethylenediamine, stir at high speed for 20 minutes, transfer to rotary evaporator...

Embodiment 2

[0060] 1. Preparation of reactive urethane-silicon-acrylate polymer

[0061] Add 22g of polyether siloxane diol IM22 and 20g of polypropylene glycol PPG-1000 into a four-neck flask equipped with a stirrer and reflux condenser, and dehydrate at 100-110°C with a vacuum degree of 0.098 for 1.5 hours, and then cooled to 40°C, add 35g of isophorone diisocyanate (IPDI), 4.0g of 2,2-dimethylol propionic acid, 35g of methyl ethyl ketone, 1.35g of 1,6 hexanediol, then heat up To 85°C, react at constant temperature for 3 hours, cool to 60°C after the reaction, add 14g of hydroxyethyl methacrylate for capping, drop it in 0.5 hour, then react at constant temperature for 2 hours, cool to 45°C after the reaction, Add 3g of triethylamine to react for 10 minutes, then add 254g of deionized water and 0.8g of ethylenediamine, stir at high speed for 20 minutes, transfer to a rotary evaporator, and remove butanone at 60°C and -0.1MPa vacuum conditions, that is A reactive urethane-silicone-acryla...

Embodiment 3

[0067] 1. Preparation of reactive urethane-silicon-acrylate polymer

[0068] In a four-neck flask equipped with a stirrer and a reflux condenser, add 27g of polyether siloxane diol IM22 and 15g of polycarbonate diol PCD, at 100-110°C, the vacuum degree is 0.098 vacuum Dehydration for 1 hour, then cooling to 40°C, add 35g of diphenylmethane diisocyanate MDI, 3.5g of 2,2-dimethylolpropionic acid, 30g of acetone, 1g of 1,4 butanediol, and then heat up to 85 ℃, react at constant temperature for 4 hours, cool to 60°C after the reaction, add 16g of hydroxyethyl methacrylate for capping, complete the dropwise addition in 0.5 hours, then react at constant temperature for 2 hours, cool to 45°C after the reaction, add 3g Triethylamine was reacted for 10 minutes, then 254g of deionized water and 0.8g of ethylenediamine were added, stirred at high speed for 20 minutes, transferred to a rotary evaporator, and methyl ethyl ketone was removed under vacuum conditions of 60°C and -0.1MPa to ob...

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Abstract

The invention discloses a urethane-organic silicon-acrylic ester ternary polymerization emulsion and a preparation method thereof. The preparation method comprises the following steps: A, modifying a polyurethane dispersion by using polyethersiloxanediol, and then carrying out end capping on the polyurethane dispersion through a (methyl) hydroxyethyl acrylate monomer to form an urethane-organic silicon-acrylic ester copolymer with both ends carried with unsaturated double bonds; and B, copolymerizing the obtained urethane-organic silicon-acrylic ester copolymer and an acrylic ester monomer to prepare the urethane-organic silicon-acrylic ester polymerization emulsion. The preparation method disclosed by the invention realizes that urethane and organic silicon structures are directly introduced to the molecular structure of polyacrylate, so that the acrylic ester improved through the method not only keeps the inherent advantages of polyacrylate, but also has the advantages of better dry-wet rubbing fastness and more softness in hand feeling in the coating printing finishing of a fabric by effectively utilizing the synergistic effect of two functional materials, namely polyurethane and organic silicon.

Description

technical field [0001] The invention belongs to the technical field of paint printing of textile materials, and relates to a terpolymer emulsion for preparing paint printing adhesives, in particular to a ternary copolymer emulsion of polyurethane, organic silicon and acrylate and a preparation method thereof. Background technique [0002] Chinese Patent Application No. 200310112823.5 proposes a method for preparing a polyurethane-acrylate water-dispersible resin. The resin particles are first prepared with a carboxyl-containing polyurethane prepolymer under the condition of using a nucleated ethylenic organosilicon monomer as a medium. Polyurethane prepolymer is formed after neutralization and water dispersion, after chain extension, polymerizable ethylenic monomers are added, and free radical polymerization is formed into a water-dispersed resin with a core-shell structure in the presence of an initiator; Chinese patent application number 200610096300.X A method for prepari...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08F290/06C08F220/16C08F212/08C08F220/26C08F220/18C08F220/14C08G18/83C08G18/76C08G18/66C08G18/61C08G18/48C08G18/34C08G18/32C08G18/75C08G18/44D06P1/52
Inventor 苏勇邹小芬丁之
Owner 深圳天鼎新材料有限公司
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