Halogen-free poly(alkylene phosphates)

Patent metadata

Field	Value
Publication number	US-9920081-B2
Application number	US-201313942128-A
Country	US
Kind code	B2
Filing date	Jul 15, 2013
Priority date	Jul 20, 2012
Publication date	Mar 20, 2018
Grant date	Mar 20, 2018

Abstract

The present invention relates to halogen-free oligomer mixtures of poly(alkylene phosphates), production of these and use as flame retardants, and also to flame-retardant polyurethanes comprising halogen-free oligomer mixtures as flame retardants.

First claim

What is claimed is:

1. An oligomer mixture consisting essentially of at least three different poly(alkylene phosphates) of the formula (I),

in which
R 1 , R 2 , R 3 and R 4 mutually independently are a straight-chain or branched C 1 -C 8 -alkyl moiety or a straight-chain or branched C 1 -C 4 -alkoxyethyl moiety,
A is a straight-chain, branched and/or cyclic C 4 -C 20 -alkylene moiety, or
a moiety of the formula —CH 2 —CH═CH—CH 2 —,
a moiety of the formula —CH 2 —C≡C—CH 2 —,
a moiety of the formula —CHR 5 —CHR 6 —(O—CHR 7 —CHR 8 ) a —, in which R 5 , R 6 , R 7 and R 8 are mutually independently methyl or H, wherein at least one of R 5 , R 6 , R 7 and R 8 is H,
a moiety of the formula —CHR 5 —CHR 6 —S(O) b —CHR 7 —CHR 8 —, or a moiety of the formula —(CHR 5 —CHR 6 —O) c —R 9 —(O—CHR 7 —CHR 8 ) d —, in which R 5 , R 6 , R 7 and R 8 are mutually independently H or mehtyl,
and
a is an integer from 1 to 5,
b is an integer from 0 to 2,
c and d are mutually independently an integer from 1 to 5,
and
R 9 is a moiety of the formula —CH 2 —CH═CH—CH 2 —, a moiety of the formula —CH 2 —C≡C—CH 2 —, a 1,2-phenylene moiety, a 1,3-phenylene moiety, a 1,4-phenylene moiety, a moiety of the formula (II)

a moiety of the formula (III)

a moiety of the formula (IV)

a moiety of the formula —C(═O)—R 12 —C(═O)—,
where
 R 10 and R 11 are mutually independently respectively H or C 1 -C 4 -alkyl or R 10 and R 11 together are an optionally alkyl-substituted ring having from 4 to 8 carbon atoms, and
 R 12 is a straight-chain, branched and/or cyclic C 2 -C 8 -alkylene moiety, a 1,2-phenylene moiety, a 1,3-phenylene moiety, or a 1,4-phenylene moiety, and

n is an integer from 0 to 100,
with the proviso that the at least three poly(alkylene phosphates) of the formula (I) differ from one another at least in the number n of the repeating units, and an average number of the repeating units n of the at least three poly(alkylene phosphates) of the formula (I) is greater than 1.10 and smaller than 2.00.

2. The oligomer mixture according to claim 1 , wherein:
R 1 , R 2 , R 3 and R 4 are identical and are ethyl, n-propyl, isopropyl, n-butyl, isobutyl or n-butoxyethyl,
A is a straight-chain C 4 -C 6 -alkylene moiety, or a moiety of the formulae

or a moiety —CHR 5 —CHR 6 —(O—CHR 7 —CHR 8 ) a —, in which a is an integer from 1 to 2 and R 5 , R 6 , R 7 and R 8 are identical and are H,
or a moiety —(CHR 5 —CHR 6 —O) c —R 9 —(O—CHR 7 —CHR 8 ) d —, in which c and d are mutually independently an integer from 1 to 2, R 5 , R 6 , R 7 and R 8 are identical and are H, and R 9 is a moiety of the formula (II), where R 10 and R 11 are identical and are methyl, and

n is an integer from 0 to 20.

3. The oligomer mixture according to claim 1 , wherein the average number of the repeating units n is greater than 1.20 and smaller than 1.90.

4. The oligomer mixture according to claim 1 , wherein the oligomer mixture is halogen-free.

5. The oligomer mixture according to claim 1 , wherein the oligomer mixture has a dynamic viscosity of 20 to 1000 mPas at 23° C.

6. A process for producing an oligomer mixture according to claim 1 , the process comprising:
reacting in a first stage, a dihydroxy compound of the formula HO-A-OH, in which A is defined as in claim 1 , with phosphorus oxychloride POCl 3 , where the amount used of dihydroxy compound of the formula HO-A-OH per mole of phosphorus oxychloride is more than 1.0 mol and less than 2.0 mol to produce a resultant mixture of oligomeric chlorophosphates of the formula (VIII)

in which n is an integer from 0 to 100; and
reacting in a second stage, the mixture of oligomeric chlorophosphates with at least one monohydroxy compound of the formula
M-OH  (IX),

in which M is R 1 , R 2 , R 3 or R 4 , and
the definitions of R 1 , R 2 , R 3 and R 4 are those stated in claim 1 .

7. Flame retardant preparations comprising at least one oligomer mixture according to claim 1 , one or more flame retardants B) differing from the oligomer mixture, and optionally one or more auxiliaries C).

8. The flame retardant preparation according to claim 7 , wherein the flame retardant B) is selected from the group consisting of triethyl phosphate, triphenyl phosphate, diphenyl cresyl phosphate, tricresyl phosphate, isopropylated or butylated aryl phosphates, bisphenol A bis(diphenyl phosphate), resorcinol bis(diphenyl phosphate), neopentyl glycol bis(diphenyl phosphate), tris(chloroisopropyl) phosphate, tris(dichloropropyl) phosphate, dimethyl methanephosphonate, diethyl ethanephosphonate, dimethyl propanephosphonate, diethyl phosphinic acid derivatives and diethyl phosphinic acid salts, oligomeric phosphates or phosphonates, hydroxylated phosphorus compounds, 5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide derivatives, 9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide (DOPO) and its derivatives, ammonium phosphate, ammonium polyphosphate, melamine phosphate, melamine polyphosphate, melamine, melamine cyanurate, alkyl ester of a tetrabromobenzoic acid, bromine-containing diols produced from tetrabromophthalic anhydride, bromine-containing polyols, bromine-containing diphenyl ethers, aluminium hydroxide, boehmite, magnesium hydroxide, expandable graphite and clay minerals.

9. Flams-retardant polyurethanes comprising at least one oligomer mixture according to claim 1 .

10. The flame-retardant polyurethanes according to claim 9 , wherein the flame-retardent polyurethanes comprise polyurethane foams.

11. A process for producing flame-retardant polyurethanes according to claim 9 , the process comprising reacting at least one organic polyisocyanate with at least one compound which has at least two hydrogen atoms reactive towards isocyanates in the presence of at least one oligomer mixture according to claim 1 .

12. The process according to claim 11 , further comprising using 3 to 25 parts by weight of oligomer mixture for every 100 parts by weight of compound having at least two hydrogen atoms reactive towards isocyanates.

13. The process according to claim 11 , wherein the compound having at least two hydrogen atoms reactive towards isocyanates comprises a polyether polyol.

14. The process according to claim 11 , wherein the compound having at least two hydrogen atoms reactive towards isocyanates comprises a polyester polyol.

15. Mouldings, lacquers, adhesives, coatings, adhesion promoters and fibres comprising polyurethanes according to claim 9 .

16. An oligomer mixture comprising poly(alkylene phosphates), wherein the poly(alkylene phosphates) in the mixture consist of at least three diff

Assignees

• Lanxess Deutschland Gmbh

Inventors

• Hansel Jan-Gerd
• Tebbe Heiko

Classifications

• C08K2201/014

  Additives containing two or more different additives of the same subgroup in C08K · CPC title

• C08L75/08

  from polyethers · CPC title

• C08L75/06

  from polyesters · CPC title

• C08G18/4825

  Polyethers containing two hydroxy groups (C08G18/4833 - C08G18/5096 take precedence) · CPC title

• C08K5/521

  Esters of phosphoric acids, e.g. of H3PO4 · CPC title