Temporary adhesive containing polysiloxane that contains heat resistant polymerization inhibitor
A polyorganosiloxane, temporary bonding technology, applied in the direction of adhesive additives, non-polymer adhesive additives, adhesives, etc., can solve problems such as detachment or offset, achieve simple removal, excellent heat resistance, Excellent effect of spin coatability
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Synthetic example 1
[0097] Preparation of the component (A) of the adhesive
[0098] As polysiloxane (a1), 10.00 g of a base polymer (manufactured by Wakka-Chemie Co., Ltd.) formed by Mw6900 vinyl group-containing MQ resin as polysiloxane (a1) and vinyl group-containing polysiloxane (a1) as polysiloxane (a1) were prepared. 3.90 g of linear polydimethylsiloxane (manufactured by Wacker Chemical Co., Ltd.), and linear polydimethylsiloxane (manufactured by Wacker Chemical Co., Ltd.) containing SiH groups with a viscosity of 70 mPa·s as polysiloxane (a2) ) 1.168 g, 0.77 g of SiH group-containing linear polydimethylsiloxane (manufactured by Wacker Chemical) having a viscosity of 40 mPa·s as polysiloxane (a2), and 0.77 g as alkynyl alcohol polymerization inhibitor (B) 0.042 g of 1,1-diphenyl-2-propyn-1-ol (manufactured by TCL) and 3.90 g of 5-nonanone (manufactured by TCL) as the solvent (C) were mixed with a stirrer (manufactured by Shinky, Awatori Rentaro) was stirred.
[0099] Separately, 0.1 g of a ...
Synthetic example 2
[0101] The same procedure as in Synthesis Example 1 was performed except that 2-phenyl-3-butyn-2-ol (manufactured by ALDRICH) was used instead of 1,1-diphenyl-2-propyn-1-ol. Modulation, as sample 2.
Synthetic example 3
[0103] Sample 3 was prepared in the same manner as in Synthesis Example 1 except that 1-ethynylcyclohexanol (manufactured by Wacker Chemical Co., Ltd.) was used instead of 1,1-diphenyl-2-propyn-1-ol.
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