Defoaming formulations containing organopolysiloxanes
A technology of polysiloxane and defoamer, applied in the field of defoamer and defoamer formulation, can solve problems such as viscosity increase
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Embodiment 1
[0317] Preparation of organosilicon compound (A):
[0318]a) Silicone compound A1 :
[0319] In a 500 mL three-necked flask, balance 101.0 g of dimethylsiloxy and vinyldimethylsiloxy units having an iodine value of 22.0 with 2.7 g of trimethylsiloxy units Hydrolyzate of hydromethyldichlorosilane end-capped and having about 55 Si units, 120.0 g of a product having a viscosity of 62 mm 2 / s (25.0°C; capillary II) of OH-terminated polydimethylsiloxane and 28.6g of polydimethylsiloxane with a viscosity of 35mm 2 / s (25.0 ° C; II capillary) the balance of dimethylsiloxy and trimethylsiloxy units at 120 ° C and 250 mbar under reduced pressure with 250 ppm PNCl 2 Equilibrate for 2 hours. By adding NaHCO 3 deactivate the catalyst. After filtration and removal of volatile components at 160 °C and a reduced pressure of 40 mbar, a product having a viscosity of 81 mm is obtained 2 / s (25.0°C; capillary II), polysiloxane with iodine value 13.3 and H content 0.016wt% A1 . 29 Si-N...
Embodiment 2
[0325] Preparation of organopolysiloxane (1):
[0326] a)Organopolysiloxane (1-1) :
[0327] In a 250mL three-necked flask, dissolve 100.0g of polysiloxane in 50mL of xylene A1 Together with 0.2 g of Karstedt Pt catalyst in toluene solution (Pt content: 0.3 wt %) heated to 90° C. for 3.5 h. During the final cooling, 0.3 g of diallyl maleate was added. The xylenes were removed at 90° C. and a reduced pressure of 32 mbar. A polysiloxane with a viscosity of 425 mPa·s (measured at 25° C. and a shear rate of 1 L / s) is obtained (1-1) .
[0328] Therefore, organopolysiloxane (1-1) The preparation uses only polysiloxane A1 , and the main component thus present is the structural element (IV), where x=52. (1-1) In the form of a non-gelling, flowable compound. Therefore, it is not necessary to use an inert solvent.
[0329] b)Organopolysiloxane (1-2) :
[0330] In a 250mL three-necked flask, 100.0g polysiloxane A2 Together with 55.0 g of linear vinyldimethylsilyl-terminate...
Embodiment 3
[0339] Preparation of non-inventive de1 defoamer formulations VC1, VC2 and VC3 using organopolysiloxanes (1-3) and V1:
[0340] To prepare antifoam formulations, substances (1), (2), (3), (6), (7) and (9) in Table 1 were mixed with solvent and heated to 150° C. for 4 hours. After cooling, components (5) and (8) are introduced again using solvent and homogenized.
[0341] General procedure for the preparation of antifoam formulations C1-C21 according to the invention using organopolysiloxanes (variant 1) :
[0342] To prepare the antifoam formulation, the substances (1), (2), (3), (4), (6), (7) and (9) in Table 1 were mixed with solvent and heated to 150°C for 4 hours . After cooling, components (5) and (8) are introduced again using solvent and homogenized.
[0343] Antifoam formulations C1-C21 according to the invention with organopolysiloxanes can also be prepared as follows (variant 2):
[0344] To prepare antifoam formulations, substances (1), (2), (3), (6), (7) an...
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