Hydrophobic epoxide modified polyoxyalkylene diamines and thickened aqueous fluids

Abstract
Aqueous fluids are thickened with epoxide modified polyoxyalkylene diamines. The polyoxyalkylene diamines are of the formula:H.sub.2 NCH(CH.sub.3)CH.sub.2 O(CH.sub.2 CH(R)O).sub.x CH.sub.2 CH(CH.sub.3)NH.sub.2wherein:R is methyl or hydrogen andx is a number selected to give the diamine a molecular weight of 3000 to 9000.The epoxide is a hydrophobic monoepoxide, diepoxide or mixture thereof.The aqueous fluid optionally incorporate ethylene glycol. They are useful for water/glycol base hydraulic fluids, cosmetics and surfactants.
Description

BACKGROUND OF THE INVENTION
1. Field of the Invention
The invention relates to epoxide modified polyoxyalkylene diamine mixtures and thickened aqueous fluids therefrom. More specifically, the invention relates to aqueous fluids thickened with a selected 3000 to 9000 molecular weight polyoxyalkylene diamine reacted with a hydrophobic epoxide.
The thickened fluids are useful for water/glycol based hydraulic fluids, cosmetics and surfactant solutions.
2. Other Thickeners in the Field
U.S. Pat. No. 4,396,499 to McCoy et al. discloses water-soluble salts of polymers prepared by the reaction of polyoxyalkylene diamines and diepoxides. The diamines are of the formula: H.sub.2 NCH(CH.sub.3)CH.sub.2 O(CH.sub.2 CH(R)O).sub.x CH.sub.2 CH(CH.sub.3)NH.sub.2.
U.S. Pat. No. 4,606,837 to McEntire et al. discloses water-glycol fluids made from polyoxyalkylene thickeners. These thickeners are prepared by the reaction of ethylene oxide with a 10 to 50 carbon atom hydrophobe such as dinonylphenol in a specified ratio.
U.S. Pat. Nos. 4,310,436 and 4,354,956 to Camp disclose polyethylene glycol fatty acid diesters used as thickening agents. U.S. Pat. No. 4,395,351 to Camp discloses ethylene oxide adducts of coconut fatty acid amine, coco fatty acid and oleic acid for use as thickeners.
U.S. Pat. No. 4,390,440 to Schwartz et al. discloses a carboxylic acid having 5 to 20 carbon atoms, a thickener which is a polyether polyol of molecular weight of 1000 to 40,000 prepared by reacting ethylene oxide with at least one active hydrogen-containing compound and at least one alpha-olefin oxide or alcohol or glycidyl ether.
U.S. Pat. No. 3,992,312 to Genjida et al. discloses thickeners comprising a water-soluble polymer. The polymer contains a polyamide residue bonded to an oxyalkylene chain. Suitable polyamides include the condensation product of a polycarboxylic acid and a polyamine. Examples of polycarboxylic acids include adipic acid and polymerized fatty acids (dimer acids). Suitable polyamines include aliphatic polyamines such as ethylene diamine, propylene diamine and butylene diamine.
SUMMARY OF THE INVENTION
The invention concerns water based fluids comprising an effective amount of a thickener. The thickener is the reaction product of a polyoxyalkylene diamine and a hydrophobic monoepoxide, diepoxide or mixture thereof. The diamine is of the formula:
H.sub.2 NCH(CH.sub.3)CH.sub.2 O(CH.sub.2 CH(R)O).sub.x CH.sub.2 CH(CH.sub.3)NH.sub.2.
About 1% to 30% of R is methyl with the balance being hydrogen. The number x is a value that specifies the molecular weight of the polyoxyalkylene diamine in the range of 3000 to 9000. The hydrophobic epoxide is a monoepoxide, diepoxide or mixture thereof. The ratio of amine equivalent: monoepoxide ranges from 1:1 to 1:1.9 and the ratio of amine equivalent: diepoxide ranges from 1:0.08 to 1:0.12.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
The thickeners of the invention are useful for thickening water or an aqueous solution of organic solvents. These thickeners have a relatively low molecular weight for their effectiveness in thickening. Low molecular weight thickeners are more stable to shear degradation than high molecular weight thickeners. This makes them useful for thickening water and water/glycol based hydraulic fluids where resistance to thinning with use is an important consideration.
A variety of monoepoxides are useful for the instant thickeners. Among these are the epoxides of 8 to 22 carbon number alpha olefin oxides and 8 to 22 carbon number alkyl glycidyl ethers. Particularly preferred are the epoxides of 8 to 14 carbon number alpha olefin oxides and 8 to 14 carbon number alkyl glycidyl ethers.
A variety of diepoxides are useful for the instant thickeners. These include the diglycidyl ethers of 4,4'-isopropylidenediphenol (bisphenol A); 4,4-isopropylidenebis (2,6-dibromophenol) (tetrabomo bisphenol A); resorcinol; neopentylglycol; 1,4-butanediol and poly(oxypropylene)gycol. The diglycidyl ethers of bisphenol A, resorcinol and 1,4-butanediol are preferred. These diepoxides are prepared by the reaction of epichlorohydrin with a hydroxyl compound.
Other useful diepoxides prepared by epoxidation with peracetic acid include vinylcyclohexene dioxide;
3,4-epoxycyclohexylmethyl 3,4-epoxycyclohexane carboxylate;
3-(3,4-epoxycyclohexane)-8,9-epoxy-2,4-dioxaspiro[5,5]-undecane;
bis(2,3-epoxycyclopentyl)ether and
bis(3,4-epoxy-6-methylcyclohexylmethyl)adipate.
Diamines used to formulate the thickeners of the invention are commercially available as Jeffamine.RTM. ED-6075, ED-6000 and ED-4000. The amine function gives the thickener reserve alkalinity and provides rust inhibition.
The thickener formulations are prepared by stirring the constituents in a stainless steel kettle at 60.degree. C. to 100.degree. C. The blends are then diluted with the desired amount of water or organic solvent to make the concentrate. The fluids are shipped as concentrates. Before use they are diluted with water and optionally ethylene glycol, typically 1 wt % to 30 wt % concentrate in water.
This invention is shown by way of example.





EXAMPLE
Jeffamine.RTM. ED-6075 is a 5400 molecular weight polyoxyalkylene diamine product made by Ni/Cu/Cr catalyzed reductive amination of a corresponding polyoxyalkylene diol consisting of 75% of oxyethylene units and 22% of oxypropylene units ramdomly distributed in the main segment and 3% oxypropylene units at the end of the polymer chain. The reductive amination was conducted in a 1.5 liter tubular reactor filled with 1.2 liter of Ni/Cu/Cr catalyst (described in U.S. Pat. No. 3,654,370 to Yeakey, incorporated herein by reference) maintained at 204.degree. C. and 2000 psia pressure. The polyoxyalkylene diol, ammonia and hydrogen were fed to the reactor at respective rates of 0.43 lb/hr., 1.04 lb/hr. and 35 liter/hr. The reactor effluent was collected for the last 23 hour period of the 26 hour period. The effluent was stripped of volatiles and analyzed as followed: 0.37 meq/g total acetylable, 0.30 meq/g total amines, 0.28 meq/g primary amines and 0.05 wt % water. The melting point of this product was 30.degree. C.
Jeffamine.RTM. ED-6000 is a 6350 molecular weight polyoxyalkylene diamine product made by Ni/Cu/Cr catalyzed reductive amination of a corresponding polyoxyalkylene diol consisting of mostly oxyethylene units and 3.5% of oxypropylene units at the end of the polymer chain. The reductive amination reaction was conducted in a similar manner as for ED-6075. The stripped product analyzed as followed: 0.315 meq/g total acetylable, 0.27 meq/g total amine, 0.25 meq/g primary amines and 0.05 wt % water. The melting point of the product was 57.degree. C.
Jeffamine.RTM. ED-4000 is a 3846 molecular weight polyoxyalkylene diamine product made by Ni/Cu/Cr catalyzed reductive amination of a corresponding polyoxyalkylene diol consisting of mostly oxyethylene units and 3.5% of oxypropylene units at the end of the polymer chain. The reductive amination reaction was conducted in a similar manner as for ED-6075. The stripped product was analyzed as followed: 0.52 meq/g total acetylable, 0.45 meq/g total amine, 0.43 meq/g primary amine and 0.23% water. The melting point of the product was 54.degree. C.
EXAMPLE I
General Synthesis
Quantities of polyoxyalkylene diamine and n-alkyl glycidyl ether were admixed in a glass vial at 60.degree. C. and then heated to 115.degree. C. for a period of 20 hours. No catalyst was used. However an acid or base catalyst is appropriate for some reagents. The completion of the addition of amine to epoxide was indicated when a 10% aqueous solution of the resulting product was clear at temperatures below the cloud point of the product. The results of these reactions are summarized in Table I.
Heloxy.RTM.WC-7 is a mixture of C.sub.8 and C.sub.10 linear alkyl glycidyl ethers, 3.92 meq/g epoxide. Heloxy.RTM. WC-8 is a mixture of C.sub.12 and C.sub.14 linear alkyl glycidyl ethers, 3.13 meq/g epoxide. Both are a product of Wilmington Chemical Co.
TABLE I__________________________________________________________________________ (a.) (b.) Viscosity Vis cs @ 40.degree. C. % Wt % RequiredJeffamine .RTM. Amount Amount cs @ 100.degree. F. aqueous ethylene glycol for 40 cs VisExample Diamine (gram) Epoxide (gram) 10% in water 10% 15% 20% @ 40.degree.__________________________________________________________________________ C.I-1. ED-6000 None 2.5 cs 2. ED-6075 None 2.5 3. ED-4000 None 4. ED-6000 40.0 Heloxy .RTM. WC-7 4.50 12.7 14.6 cs 79.4 cs 180 cs 12.0 wt % 5. ED-6000 40.0 Heloxy .RTM. WC-7 2.25 32.0 34.0 191 492 10.5 Heloxy .RTM. WC-8 2.25 6. ED-6000 40.0 Heloxy .RTM. WC-8 4.50 126 52.0 278 840 9.5 7. ED-6000 40.0 Heloxy .RTM. WC-7 4.80 197 42.9 174 447 10.0 8. ED-6000 40.0 Heloxy .RTM. WC-7 2.40 182 38.0 215 609 10.0 Heloxy .RTM. WC-8 2.40 9. ED-6000 40.0 Heloxy .RTM. WC-8 4.80 Jelly 435 5636 19837 5.510. ED-6075 50.0 Heloxy .RTM. WC-7 6.00 9.7 14.0 40.2 134 15.011. ED-6075 50.0 Heloxy .RTM. WC-7 3.00 19.3 31.2 69.4 227 11.5 Heloxy .RTM. WC-7 3.0012. ED-6075 50.0 Heloxy .RTM. WC-8 6.00 58.4 36.5 141 396 10.513. ED-6075 44.0 Heloxy .RTM. WC-7 6.00 139 33.5 170 576 10.514. ED-6075 44.0 Heloxy .RTM. WC-7 3.0015. Heloxy .RTM. WC-8 3.00 296 60.5 641 2003 9.516. ED-6075 44.0 Heloxy .RTM. WC-8 6.00 55.6 88.5 875 3611 8.517. ED-4000 40.0 Heloxy .RTM. WC-8 7.13 50.0 54.0 352 1809 9.018. ED-4000 40.0 Heloxy .RTM. WC-7 7.13 64.0 24.0 96 360 11.7__________________________________________________________________________ (a.) Solution in 1:1 w/w ethylene glycol/water (b.) Solution in 1:1 w/w ethylene glycol/water formulated for a fire resistant hydraulic fluid.
EXAMPLE II
General Synthesis
Quantities of polyoxyalkylene diamine, n-alkyl glycidyl ether and diglycidyl ether were admixed in a glass vial at 60.degree. C. and then heated to 115.degree. C. for a period of 20 hours. No catalyst was used. However an acid or base catalyst is appropriate for some reagents. The completion of the addition of amine to epoxide was indicated when a 10% aqueous solution of the resulting product was clear at temperatures below the cloud point of the product. The results of these reactions are summarized in Table II.
Epon.RTM. 828 is the diglycidyl ether of bisphenol A, 5.26 meq/g. It is a product of Shell Chemical Co.
Heloxy.RTM. WC-67 is the diglycidyl ether of 1,4-butanediol, 8.11 meq/g epoxide. Heloxy.RTM. WC-68 is the diglycidyl ether of neopenty glycol, 7.46 meq/g epoxide. Both are a product of Wilmington Chemical Co.
TABLE II__________________________________________________________________________ (a.) (b.) Viscosity Vis cs @ 40.degree. C., % Wt % RequiredExam- Jeffamine .RTM. Amount Amount cs @ 100.degree. F. aqueous ethylene glycol For 40 cs Visple Diamine (gram) Diepoxide (gram) 10% in water 10% 15% 20% @ 40.degree.__________________________________________________________________________ C.II-1. ED-6000 None 2.5 2. ED-6075 None 2.5 3 ED-4000 None 2.4 4. ED-6000 23.1 Epon .RTM. 828 0.9 5.0 12.4 cs 26.5 cs 49.6 cs 17.2 wt % 5. ED-6000 22.8 Epon .RTM. 828 1.2 4.9 20.0 59.9 130 14.4 6. ED-6000 22.5 Epon .RTM. 828 1.5 Jelled *6%-32.6 6.7 *8%-187.1 7. ED-6000 40.0 Heloxy .RTM. WC-67 4.2 4.35 12.8 24.7 48.6 19.0 8. ED-6000 40.0 Heloxy .RTM. WC-67 4.6 3.20 9.3 40.1 79.6 15.0 9. ED-6000 40.0 Heloxy .RTM. WC-68 4.2 3.50 9.8 17.8 29.5 24.510. ED-6000 40.0 Heloxy .RTM. WC-68 5.0 4.38 12.7 24.4 46.8 17.511. ED-6075 38.0 Epon .RTM. 828 2.0 12.3 20.1 40.6 106 14.212. ED-6075 37.5 Epon .RTM. 828 2.2 23.4 27.2 64.7 166 12.513. ED-6075 37.6 Epon .RTM. 828 2.4 59.2 43.5 139 276 9.514. ED-6075 37.4 Epon .RTM. 828 2.6 276 89 400 1347 7.015. ED-4000 40.0 Epon .RTM. 828 2.5 4.6 10.6 22.5 40.8 20.016. ED-4000 40.0 Epon .RTM. 828 2.8 .34 16.8 37.7 80.5 15.517. ED-4000 40.0 Epon .RTM. 828 3.1 10.9 20.4 48.4 103 14.018. ED-6075 40.0 Heloxy .RTM. WC-68 5.0 4.6 11.3 26.3 52.9 19.019. ED-6075 40.0 Heloxy .RTM. WC-67 4.5 6.0 32.8 71.9 161.0 12.0__________________________________________________________________________ (a.) Solution in 1:1 w/w ethylene glycol/water (b.) Solution in 1:1 w/w ethylene glycol/water formulated for a fire resistant hydraulic fluid. *Vis cs @ 40.degree. F., 6% and 8% in aqueous ethylene glycol.
EXAMPLE III
General Synthesis
Quantities of polyoxyalkylene diamine, n-alkyl glycidyl ether and diglycidyl ether were admixed in a glass vial at 60.degree. C. and then heated to 115.degree. C. for a period of 20 hours. No catalyst was used. However an acid or base catalyst is appropriate for some reagents. The completion of the addition of amine to epoxide was indicated when a 10% aqueous solution of the resulting product was clear at temperatures below the cloud point of the product. The results of these reactions are summarized in Table III.
TABLE III__________________________________________________________________________ (a.) (b.) Viscosity Vis cs @ 40.degree. C., % Wt % RequiredJeffamine .RTM. Amount Amount cs @ 100.degree. F. aqueous ethylene glycol For 40 cs VisExample Diamine (gram) Epoxide (gram) 10% in water 10% 15% 20% @ 40.degree.__________________________________________________________________________ C.III-1. ED-6000 None 2.4 cs 2. ED-6075 None 2.5 3. ED-4000 None 2.4 4. ED-6000 40.0 Heloxy .RTM. WC-7 2.25 16.6 15.5 cs 46.9 cs 96.7 cs 14.5 wt % Epon .RTM. 828 1.05 5. ED-6000 40.0 Heloxy .RTM. WC-7 1.05 25.3 21.7 64.5 159 12.2 Heloxy .RTM. WC-8 1.05 Epon .RTM. 828 1.05 6. ED-6000 40.0 Heloxy .RTM. WC-8 2.25 45.6 7.3 41.8 214.6 15.0 Epon .RTM. 828 1.05 7. ED-6000 50.0 Heloxy .RTM. WC-7 3.30 98.4 32.0 131 412 10.7 Epon .RTM. 828 1.65 8. ED-6000 50.0 Heloxy .RTM. WC-7 1.65 849 122 957 29.0 7.5 Heloxy .RTM. WC-8 1.65 Epon .RTM. 828 1.65 9. ED-6000 50.0 Heloxy .RTM. WC-8 3.30 4174 142 1040 38.1 7.5 Epon .RTM. 828 1.6510. ED-6075 50.0 Heloxy .RTM. WC-7 3.80 82 29.0 85.7 208 9.5 Epon .RTM. 828 1.6511. ED-6075 50.0 Heloxy .RTM. WC-7 1.65 258 52 244 594 9.0 Heloxy .RTM. WC-8 1.65 Epon .RTM. 82812. ED-6075 50.0 Heloxy .RTM. WC-8 3.30 232 45.3 252 743 11.5 Epon .RTM. 828 1.6513. ED-6000 50.0 Heloxy .RTM. WC-7 1.05 43.5 28.9 104 215 12.8 Heloxy .RTM. WC-8 3.3014. ED-6000 50.0 Heloxy .RTM. WC-68 1.15 60.6 34.2 132 308 10.5 Heloxy .RTM. WC-8 3.3015. ED-6075 50.0 Heloxy .RTM. WC-67 1.05 39.1 26.5 63.9 312 12.5 Heloxy .RTM. WC-8 3.3016. ED-6075 50.0 Heloxy .RTM. WC-68 1.10 38.4 35.2 146 679 10.5 Heloxy .RTM. WC-8 3.3017. ED-4000 40.0 Heloxy .RTM. WC-8 5.8 Jelly 899 15380 3688 5.5 Epon .RTM. 828 1.018. ED-4000 40.0 Heloxy .RTM. WC-7 5.8 75 63 332 875 8.5 Epon .RTM. 828 1.919. ED-6075 50.0 Heloxy .RTM. WC-8 3.35 46.6 35.9 128 393 10.5 Heloxy .RTM. WC-68 1.2020. ED-6075 50.0 Heloxy .RTM. WC-8 3.30 35.2 37.4 197 727 10.5 Heloxy .RTM. WC-68 1.40__________________________________________________________________________ a. Solution in 1:1 w/w ethylene glycol/water b. Solution in 1:1 w/w ethylene glycol/water formulated for a fire resistant hydraulic fluid.
While particular embodiments of the invention have been described, it is well understood that the invention is not limited thereto since modifications may be made. It is therefore contemplated to cover by the appended claims any such modifications as fall within the spirit and scope of the claims.
Claims
  • 1. An aqueous fluid comprising an effective thickening amount of a thickener comprising the reaction product of:
  • a. a polyoxyalkylene diamine of the formula:
  • H.sub.2 NCH(CH.sub.3)CH.sub.2 O(CH.sub.2 CH(R)O).sub.x CH.sub.2 CH(CH.sub.3)NH.sub.2
  • wherein: from 1% to 30% of R is methyl and the remaining R is hydrogen, and x is a number such that the molecular weight of the polyoxyalkylene diamine ranges from 3000 to 9000; with
  • b. a mixture of a hydrophobic monoepoxide comprising a C.sub.8 to C.sub.22 alpha olefin of alkyl glycidyl ether and a hydrophobic diepoxide
  • wherein: the ratio amine equivalent: monoepoxide: diepoxide in the range of 1:0.25:0.25 to 1:1.4:1.
  • 2. The aqueous fluid of claim 1 wherein the monoepoxide is a C.sub.8 to C.sub.14 alpha olefin or alkyl glycidyl ether.
  • 3. The aqueous fluid of claim 1 wherein the amount of thickener is from 1 wt % to 30 wt %.
  • 4. The aqueous fluid of claim 1 wherein the aqueous fluid additional comprises ethylene glycol.
  • 5. An aqueous fluid comprising the reaction product of:
  • a. a polyoxyalkylene diamine of the formula:
  • H.sub.2 NCH(CH.sub.3)CH.sub.2 O(CH.sub.2 CH(R)O).sub.x CH.sub.2 CH(CH.sub.3)NH.sub.2
  • wherein: from 1% to 30% of R is methyl and the remaining R is hydrogen, and x is a number such that the molecular weight of the polyoxyalkylene diamine ranges from 3000 to 9000; with
  • b. a hydrophobic monoepoxide comprising a C.sub.8 to C.sub.22 alpha olefin or alkyl glycidyl ether
  • wherein: the ratio amine equivalent: epoxide is in the range of 1:1 to 1:1.9.
  • 6. The composition of claim 5 wherein the hydrophobic monoepoxide is a C.sub.8 to C.sub.14 alpha olefin glycidyl ether.
  • 7. The composition of claim 5 wherein the hydrophobic monoepoxide is a C.sub.8 to C.sub.14 alkyl glycidyl ether.
  • 8. The aqueous fluid of claim 5 wherein the amount of thickener is from 1 wt % to 30 wt %.
  • 9. The aqueous fluid of claim 5 which additionally comprises ethylene glycol.
US Referenced Citations (4)
Number Name Date Kind
2792367 De Groote et al. May 1957
4390440 Schwartz et al. Jun 1983
4396499 McCoy et al. Aug 1983
4606837 McEntire et al. Aug 1986