Oxidation-resistant strong-acid-resistant organosilicon compound, and synthesis method and application thereof
A technology of organosilicon compound and synthesis method, which is applied in the field of acid mist suppression to achieve the effect of improving wettability
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Embodiment 1
[0036] A method for synthesizing an oxidation-resistant and acid-resistant organosilicon compound, comprising the steps of:
[0037] (1) 1.2g chloroplatinic acid hexahydrate (H 2 PtCl 6 ·6H 2 O) join in the 20mL isopropanol, stir, standby as initiator;
[0038] (2) Under nitrogen protection, the following components are added in proportion (mol parts) in the dry reactor:
[0039] (CH 3 ) 3 Si-O-[Si(CH 3 ) 2 -O-] 12 [Si(CH 3 )H-O-] 2 [Si(CH 3 ) 2 -O-] 12 -Si(CH 3 ) 3 100 copies
[0040] CH 2 =CH-(CH 2 ) 10 SO 3 CH 3 26 copies
[0041] Initiator 0.005 part
[0042] The above mixture was fully stirred, and heated to 95°C, and reacted for 1h under stirring. Add 100 parts of 1 mol / L sodium hydroxide solution to the product, heat to 90° C., and react for 0.5 h under vigorous stirring to obtain the oxidation-resistant and strong acid-resistant organosilicon compound.
Embodiment 2
[0044] A method for synthesizing an oxidation-resistant and acid-resistant organosilicon compound, comprising the steps of:
[0045] (1) 1.2g chloroplatinic acid hexahydrate (H 2 PtCl 6 ·6H 2 0) join in 20mL isopropanol, stir well, standby as catalyst;
[0046] (2) The following components are added in proportion (mol parts) to the dry reactor:
[0047] (CH 3 ) 3 Si-O-[Si(CH 3 ) 2 -O] 12 -[Si(CH 3 )H-O] 2 -[O-Si(CH 3 ) 2 -] 12 -O-Si(CH 3 ) 3 100 copies
[0048] CH 2 =CH-(CH 2 ) 10 -(C 6 h 4 )-PO 3 CH 3 26 copies
[0049] Catalyst 0.005 parts
[0050] Note: CH 2 =CH-(CH 2 ) 10 -(C 6 h 4 )-PO 3 CH 3 In, -(C 6 h 4 )- is phenylene.
[0051] The above mixture was fully stirred, and heated to 95°C, and reacted for 1h under stirring. Add 100 parts of 1 mol / L sodium hydroxide solution to the product, heat to 90° C., and react for 0.5 h under vigorous stirring to obtain the oxidation-resistant and strong acid-resistant organosilicon compound.
Embodiment 3
[0053] A method for synthesizing an oxidation-resistant and acid-resistant organosilicon compound, comprising the steps of:
[0054] (1) 1.2g chloroplatinic acid hexahydrate (H 2 PtCl 6 ·6H 2 0) join in 20mL isopropanol, stir well, standby as catalyst;
[0055] (2) The following components are added in proportion (mol parts) to the dry reactor:
[0056] (CH 3 ) 3 Si-O-[Si(CH 3 ) 2 -O] 12 -[Si(CH 3 )H-O] 2 -[O-Si(CH 3 ) 2 -] 12 -O-Si(CH 3 ) 3 100 copies
[0057] CH 2 =CH-(CH 2 ) 10 -C 6 h 10 -C 6 h 4 -COOH (alkenyl substituted cyclohexyl benzoic acid) 37 parts
[0058] Catalyst 0.006 parts
[0059] Note: CH 2 =CH-(CH 2 ) 10 -C 6 h 10 -C 6 h 4 -COOH, C 6 h 10 is cyclohexylene, -C 6 h 4 - is phenylene.
[0060] The above mixture was fully stirred, and heated to 95° C., and reacted for 1 h under stirring to obtain the oxidation-resistant and strong-acid-resistant organosilicon compound.
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