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Silane functional prepolymer and isocyanate functional prepolymer blend adhesive composition

A silane functional, adhesive technology, used in polyurea/polyurethane adhesives, polyether adhesives, adhesive types, etc., can solve problems such as high cost, achieve long-term durability, fast connection, fast Effect of cure rate

Active Publication Date: 2013-06-26
DDP SPECIALTY ELECTRONICS MATERIALS US LLC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Such shutdowns would be costly for automakers and must be avoided

Method used

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  • Silane functional prepolymer and isocyanate functional prepolymer blend adhesive composition
  • Silane functional prepolymer and isocyanate functional prepolymer blend adhesive composition
  • Silane functional prepolymer and isocyanate functional prepolymer blend adhesive composition

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0156] Preparation of Polyurethane Prepolymer A

[0157] Charge 336.14 g of VORANOL to a 2 liter kettle equipped with a stirrer and heating jacket under nitrogen TM 220-56 polyol, 487.13g VORANOL TM232-036 polyol, and 29.58 g of dialkyl phthalate plasticizer. The reactants were mixed and heated under nitrogen until the mixture reached 54°C. Once the mixture reached 54°C, 148.48 g of diphenylmethane 4,4'-diisocyanate (ISONATE TM 125M) and mix. Then, slowly add 0.07g METACURE dropwise TM T-9 tin catalyst. The reaction was exothermic and after the reaction temperature peaked, the reaction was held between 80°C and 85°C for 30 minutes. Then, set the temperature setting of the heating element at 60°C. Thereafter, 463.25 g of dialkyl phthalate and 14.20 g of diethyl malonate were added. The mixture was stirred for 15 minutes. Thereafter N,N'-bis(3-trimethoxypropyl)amine (21.15 g) was added to the kettle and mixed for 60 minutes. Stop the reaction and store the prepolyme...

Embodiment 1

[0159] Mix 630 g of SAX400 silane-functional prepolymer and 3 g of SILQUEST TM A171 Vinyltrimethoxysilane was charged to a 1 gallon mixer. The mixture was degassed and mixed under vacuum for 5 minutes. The vacuum was broken with nitrogen. 90 g of Prepolymer A as described above, 75 g of isocyanatopropyltrimethoxysilane and 244.5 g of alkyl phthalate plasticizer were added to the mixer. The mixture was degassed and mixed under vacuum for 5 minutes. The vacuum was broken again with nitrogen. 450 g of dry carbon black were added. Slowly apply vacuum. When half vacuum is reached, start mixing to wet out the filler for 2 minutes. The vacuum valve was then fully opened and mixing was continued for 20 minutes under full vacuum. The mixture was scraped off under nitrogen. To this mixture was added 3.0 g of LICA TM 09 and 4.5 g DDBSA, and full vacuum was applied again before additional mixing. The mixture was mixed under vacuum for an additional 10 minutes. The vacuum was b...

Embodiment 2 to 3 and comparative Embodiment 4

[0167] Three adhesive compositions were prepared using the procedure described in Example 1 using the components described in Table 2. (QKA) beads derived from these adhesives were applied to PPG-coated ODCT TM 8000 urethane clear coat on metal coupons. After 7 days of initial curing at 23°C and 50% relative humidity (RH), QKA tests were performed and the results are listed in Table 2.

[0168] In addition, the QKA beads from Example 1, Example 3, and Comparative Example 4 were applied to 1 inch by 6 inch (2.54 cm by 15.2 cm) clear glass coupons, which were tested with BETASEAL TM 43518 and BETASEAL TM 43520A Primer Primer. These QKA samples were divided into two groups after initial curing for 7 days under conditions of 23°C and 50% relative humidity (CT conditions). The first group was immediately tested with the QKA test. The second group was placed in an oven at 110°C for different periods of time before performing the QKA test. These QKA results are listed in Table ...

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Abstract

The invention is an adhesive composition comprising a) one or more silane functional prepolymers comprising a polyether or a polyolefin backbone and silane moieties capable of silanol condensation; b) one or more isocyanate functional prepolymers comprising a polyether backbone and isocyanate moieties; c) one or more organotin compounds or titanate or zirconate compounds having one or more ligands comprising a hydrocarbyl phosphate ester or a hydrocarbyl sulfonate ester, or a mixture thereof; d) a tertiary amine or an anhydrous strong organic acid which is miscible with the polymer and enhances the bonding of the adhesive to a coated unprimed substrate. In one embodiment, the invention is a method of bonding two or more substrates together using the adhesive compositions of this invention. The process comprises applying an adhesive as described herein to one or more of the substrates; contacting the one or more substrates with the adhesive disposed between the substrates; and allowing the adhesive to cure.

Description

[0001] This application is a divisional application of No. 200680039600.2 invention patent application with the filing date of October 23, 2006 and the invention name being "Adhesive Composition of Blend of Silane Functional Prepolymer and Isocyanate Functional Prepolymer". technical field [0002] The present invention relates to adhesive compositions comprising a blend of one or more silane-functional prepolymers and one or more isocyanate-functional prepolymers; The method by which materials are glued together. Preferably, the adhesive of the invention is used to bond the window to the window flange. Background technique [0003] Polyurethane sealant compositions are used to bond non-porous substrates such as glass to non-porous substrates; these are described in U.S. Patent 4,374,237 to Berger et al. and U.S. Patent 4,687,533 to Rizk et al., both incorporated This article is for reference. US Patent 4,374,237 to Berger et al. describes polyurethane sealants comprising ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C09J175/08C03C27/00
CPCC08G18/10C08G18/12C08G18/718C08G65/336C09J171/02C08G18/289C08G18/2895C08G18/2865C08G77/22C08G77/08C08L83/04C09J183/00
Inventor 朱慧德S·Z·马迪M·B·费尔德鲍希
Owner DDP SPECIALTY ELECTRONICS MATERIALS US LLC