US2005171320A1PendingUtilityA1
Continuous preparation of thermoplastically processable polyurethanes
Priority: Aug 21, 2002Filed: Feb 15, 2005Published: Aug 4, 2005
Est. expiryAug 21, 2022(expired)· nominal 20-yr term from priority
C08G 18/10C08G 18/08C08G 18/0895
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Claims
Abstract
The present invention relates to a multi-stage process for the continuous preparation of thermoplastically processable polyurethanes with improved processing properties based on various polyols
Claims
exact text as granted — not AI-modified1 . A multi-stage process for the continuous preparation of thermoplastically processable polyurethane elastomers (TPU) with tensile strengths of >30 MPa (measured in accordance with EN ISO 527-3), comprising
a) preparing a prepolymer I by reacting
A) at least one organic diisocyanate, with
B) a polyol 1 having on average at least 1.8 and not more than 3.0 Zerewitinoff-active hydrogen atoms and a number-average molecular weight {overscore (M)} n of 450 to 10,000;
b) reacting said prepolymer I prepared in a) with
C) a polyol 2, which is different than polyol 1, wherein said polyol 2 has on average at least 1.8 and not more than 3.0 Zerewitinoff-active hydrogen atoms and a number-average molecular weight {overscore (M)} n of 60 to 10,000,
to yield a prepolymer II, wherein an equivalent ratio of NCO groups to the sum of NCO-reactive groups of from 1.2:1 to 10:1 is established, based on reaction components (A), (B) and (C);
c) reacting, in a high-viscosity reactor operating with a high shear energy, said prepolymer II prepared in b) completely with:
D) at least one low molecular weight polyol or polyamine having on average at least 1.8 and not more than 3.0 Zerewitinoff-active hydrogen atoms and a number-average molecular weight {overscore (M)} n of 60 to 400 as a chain lengthener;
wherein steps a) to c) are optionally carried out in the presence of F) catalysts, and optionally, with the addition of E) 0 to 20 wt. %, based on the total amount of TPU, of further auxiliary substances and additives, with the overall equivalent ratio of NCO groups to the sum of NCO reactive groups being from 0.9:1 to 1.2:1, based on the sum of all the reaction components of steps a) to c), and wherein steps a) and b) are carried out in separate reactors and step c) is carried out in a separate reactor than steps a) and b.
2 . The process of claim 1 , wherein B) said polyol 1 and C) said polyol 2, both of which contain Zerewitinoff-active hydrogen atoms, are selected from the group consisting of (i) polyester-polyols, (ii) polyether-polyols, (iii) polycarbonate-polyols, (iv) polyols which contain nitrogen, phosphorus, sulfur and/or silicon atoms and (v) mixtures thereof.
3 . The process of claim 1 , wherein D) said low molecular weight polyols containing Zerewitinoff-active hydrogen atoms comprises ethylene glycol, butanediol, hexanediol, 1,4di-(β-hydroxyethyl)-hydroquinone, or 1,4-di(β-hydroxyethyl)-bisphenol A.
4 . The process of claim 1 , wherein A) said organic diisocyanate comprises an aromatic diisocyanate.
5 . The process of claim 4 , wherein said aromatic diisocyanate comprises a diphenylmethane-diisocyanate isomer mixture having a 4,4′-diphenylmethane-diisocyanate content of >96 wt. %.
6 - 8 . (canceled)
9 . The process of claim 1 , wherein step c) is carried out in a multi-screw extruder.Join the waitlist — get patent alerts
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