IP Library › Granted Patent US 9,505,910
Granted Patent B2
US 9,505,910 · App. 14/352,232 · Granted Nov 29, 2016

Modified diphenylmethane diisocyanate (MDI) biuret curing agent and preparation method thereof

Inventors: Jianming Zhou (Wuhan, CN); Shaoqun He (Wuhan, CN)
Assignee: J&H Xiangyang Chemical Co., Ltd.
C08K5/29C07C275/62C08G18/302C08G18/3206C08G18/3212C08G18/42C08G18/48C08G18/7671C08G18/7831C08K5/01C08K5/07C08K5/103C09D175/04
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Quick Facts
Patent No.
US 9,505,910
App. No.
14/352,232
Granted
Nov 29, 2016
Kind
B2
Abstract

Provided are a modified diphenylmethane diisocyanate (MDI) biuret curing agent and preparation method thereof, the curing agent being prepared by reacting dibasic alcohol, water and MDI in an organic solvent. The preparation method includes the steps of: firstly, using the dibasic alcohol to modify a part of MDI, dividing the metered water into multiple parts, and adding the water by multiple times; after adding the first part of water, reacting firstly under 70-100° C., then heating up to 120-140° C. for reaction; secondly, lowering the temperature to 70-100° C., adding the second part of water; and repeating the above processes until all the metered water is added, to produce the MDI curing agent with partial biuret structure. The curing agent is mainly used as the curing agent of polyurethane coating and adhesive agent, and has a higher NCO percentage and a slower curing speed than that of common MDI prepolymer curing agents.

Claims (17)

1. A preparation method of modified diphenylmethane diisocyanate (MDI) biuret curing agent, comprising the steps of:

a, adding MDI and an organic solvent in a reaction kettle, stirring uniformly, adding dehydrated dibasic alcohol for reaction at a room temperature for 0.5˜2 hours, then heating up to 60° C., reacting at 60˜90° C. for 1˜4 hours to obtain an MDI-modified product;

b, adding water by multiple times, wherein a molar ratio between the water and remaining MDI after the first step of the reaction is 1:3˜3.2, wherein the water is added within a range from 4 to 10 times; controlling the temperature in the reaction kettle within 70˜100° C., dropwise adding a first part of the water, and reacting for 0.5˜2 hours, then heating up to 120˜140° C. , and reacting for 0.5˜2 hours; lowering the temperature to 70˜100° C., dropwise adding a second part of the water, repeating the above process until all the water is added, reacting for 0.5˜2 hours, heating up to 120˜140° C. and reacting for 1˜5 hours; and

c, lowering the temperature to 60° C., adding the organic solvent according to the product solid content requirements, stirring uniformly, and discharging to obtain the modified MDI biuret curing agent;

the feeding ratios of each reactant in the curing agent are as follows: in the first step of the reaction, the molar ratio between the dibasic alcohol and the MDI is 0.05˜0.2:1; and in the second step of the reaction, the molar ratio between the water and the remaining MDI after the first step of the reaction is 1:3˜3.2,

wherein the mole number of the remaining MDI after the first step of the reaction is the difference of subtracting two times of the mole number of the dibasic alcohol from the MDI mole number fed in the first step of the reaction;

the product indexes of the curing agent are as follows:

wherein the following contents are weight percentages:

(1) solid content: 50˜75%; and

(2) NCO content: 12˜18%, counted in terms of total solid.

2. The preparation method of modified diphenylmethane diisocyanate (MDI) biuret curing agent according to claim 1 , wherein the MDI is one or a mixture of at least two of 4,4′-MDI, 4,2′-MDI and 2,2′-MDI.

3. The preparation method of modified diphenylmethane diisocyanate (MDI) biuret curing agent according to claim 1 , wherein the dibasic alcohol in step a is any one or a mixture of more than one of polyester dibasic alcohol, polyether dibasic alcohol, other dibasic alcohol or small molecule dibasic alcohol; wherein

the other dibasic alcohol is an armine ester diol, hydroxyl-terminated acrylic resin or hydroxyl-terminated alkyd resin; and wherein

the small molecule dibasic alcohol is a 3-methyl-1,5-pentanediol, neopentyl glycol, ethylene glycol, diethylene glycol, cyclohexanediol, methyl propanediol, TCD tricyclic diol, 1,3-propanediol, 1,4-bis (hydroxymethyl)cyclohexane, 1,4-butanediol, 1,3-butanediol, 1,5-pentanediol, diethyl glutarate, 1,2-propanediol, diethylene glycol, tetrahydrofuran, 1,6-hexanediol, trimethyl pentanediol, butyl ethyl propanediol, 2,2-bis (4-hydroxyphenyl) propane, hydroxyl neopentanoic acid, neopentyl alcohol esters, resoreinol bis-hydroxyethyl ether, hydroquinone bis (2-hydroxyethyl) ether, resoreinol bis-hydroxypropyl ether, resorcinol bis-hydroxypropoxy ethyl ether, 2,5-di-tert-butyl hydroquinone, dipropylene glycol, tripropylene glycol, or ethyl hexanediol.

4. The preparation method of modified diphenylmethane diisocyanate (MDI) biuret curing agent according to claim 3 , wherein the polyester dibasic alcohol is polyethylene adipate-ethylene glycol-propylene glycol diol, polyethylene adipate-butylene glycol diol, poly sebacic acid-adipic acid-ethylene glycol-neopentyl glycol ester diol, polyethylene isophthalate-adipic acid-neopentyl glycol-diethylene glycol diol, polycarbonate diol or polycaprolactone diol.

5. The preparation method of modified diphenylmethane diisocyanate (MDI) biuret curing agent according to claim 3 , wherein the polyether glycol is a polyoxypropylene diol, polyoxyethylene-polypropylene oxide diol or polytetrahydrofuran diol.

6. The preparation method of modified diphenylmethane diisocyanate (MDI) biuret curing agent according to claim 1 , wherein the organic solvent is an ester such as acetic ether, n-butyl acetate, ethylene glycol monoethyl ether acetate, propylene glycol monomethyl ether acetate, dimethyl carbonate, diethyl carbonate, diphenyl carbonate, acetone, methyl ethyl ketone, cyclohexanone, toluene, xylene, dioxane, tetrahydrofuran, N, N-dimethyl formamide, and a mixture of at least two thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 16, 2014
From: ZHOU, JIANMING; HE, SHAOQUN
To: J&H XIANGYANG CHEMICAL CO., LTD
Reel/Frame 032689/0217 →
Priority Claims (2)
CN 2011 1 0320518 · Oct 20, 2011 · national
CN 2011 1 0380099 · Nov 25, 2011 · national
Continuity (1)
Related Publication 20140252269A1 · Sep 11, 2014