US5180755A
Expired / Lapsed
US
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Method for producing antistatic polyurethane resin
Assignee: Bridgestone Corp
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Filing: 1991-06-26
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Granted: 1993-01-19
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Expires: 2011-06-26
Abstract
Abstract A method for producing antistatic polyurethane resins according to the present invention comprises a reaction of a compound having at least two active hydrogen atoms with an organic isocyanate in the presence of at least one kind of complex compounds represented by a general formula [Me(ClO 4 ) n ] x [R(OH) y ] z and being liquid at room temperature, wherein Me is an element belonging to Group I or II in the periodic table; n is a number of 1-2; x is a number of 1-5; y is a number of 1-3; z is a number of 1-6; and R is a residual group other than hydroxyl group in a polyhydric alcohol or its derivative. Me of said complex compounds is preferably Li, Na, K, Ca or Ba. As antistatic agents are liquid at room temperature in the present invention, they can be formulated uniformly within raw materials of polyurethane resins. By virtue thereof, the antistatic effect is exhibited homogeneously and so highly.
Inventors
- 👤 Kuniaki Yasunaga
- 👤 Shigeru Ueno
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-09 04:39
CPC Classifications
C; C09; C09K; C09K3/00; C09K3/16; C08; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/30; C08G18/38; C08G18/3897; C08K; C08K5/00; C08K5/0008; C08K5/0075; C08K5/0091; C08G2110/00; C08G2110/0008; C08G2110/0025
Claims Analysis
Total Claims: 6
Claim 1
Independent Claim
123 words
A method for producing antistatic flexible polyurethane resins which comprises reacting: a compound having at least two active hydrogen atoms; and an organic isocyanate; wherein said reaction takes place in the presence of at least one complex compound of formula [Me(ClO.sub.4).sub.n ].sub.x [R(OH).sub.y ].sub.z wherein said complex compound is a liquid at room temperature, and wherein Me is selected from the group consisting of group I and group II elements in the periodic table, n is a number of 1 to 2, x is a number of 1 to 5, y is a number of 1 to 3, z is a number of 1 to 6, and R is a residual group other than hydroxyl group in a polyhydric alcohol or its derivative.
Claim 2
Independent Claim
123 words
A method for producing antistatic flexible polyurethane resins which comprises reacting: a compound having at least two active hydrogen atoms; and an organic isocyanate; wherein said reaction takes place in the presence of at least one complex compound of formula [Me(ClO.sub.4).sub.n ].sub.x [R(OH).sub.y ].sub.z wherein said complex compound is a liquid at room temperature, and wherein Me is selected from the group consisting of group I and group II elements in the periodic table, n is a number of 1 to 2, x is a number of 1 to 5, y is a number of 1 to 3, z is a number of 1 to 6, and R is a residual group other than hydroxyl group in a polyhydric alcohol or its derivative.
Claim 3
Dependent Claim
25 words
A method for producing antistatic polyurethane resins according to claim 1, in which Me of said complex compounds is Li, Na, K, Ca or Ba.
Claim 4
Dependent Claim
23 words
A method for producing antistatic polyurethane resins according to claim 1 or 2, wherein the polyurethane resins are soft or rigid polyurethane foams.
Claim 5
Dependent Claim
20 words
A method for producing antistatic polyurethane resins according to claim 1 or 2, wherein the polyurethane resins are polyurethane films.
Claim 6
Dependent Claim
83 words
A method as claimed in claim 1, wherein the polyhydric alcohol R(OH) y is selected from the group consisting of ethyleneglycol, ethyleneglycol monomethylether, ethyleneglycol monoethylether, ethyleneglycol monoisopropylether, ethyleneglycol monobutylether, ethyleneglycol monoisoamylether, ethyleneglycol monophenylether, ethyleneglycol monobenzylether, ethyleneglycol monohexylether, diethyleneglycol, diethyleneglycol monomethylether, diethyleneglycol monoethylether, diethyleneglycol monobutylether, diethyleneglycol acetate, triethyleneglycol, triethyleneglycol monomethylether, triethyleneglycol monoethylether, triethyleneglycol monobutylether, tetraethyleneglycol, polyethyleneglycol, propyleneglycol, propyleneglycol monomethylether, propyleneglycol monoethylether, propyleneglycol monobutylether, dipropyleneglycol, dipropyleneglycol monomethylether, dipropyleneglycol monoethylether, tripropyleneglycol, tripropyleneglycol monomethylether, polypropyleneglycols, trimethyleneglycol, 1,4-butanediol, 1,5-pentandiol, hexyleneglycol, octyleneglycol, glycerin, glycerin mono-or di-acetate and glycerin monobutylate.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1996-01-19 | 1996-07-20 | 1997-01-19 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 2000-01-19 | 2000-07-20 | 2001-01-19 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2004-01-19 | 2004-07-20 | 2005-01-19 | $7700.00 | Window Closed / Lapsed |