Coalescing agent derived from succinate ester

Abstract

The present invention relates to a coalescing agent and a coating composition containing the coalescing agent as represented in structure (I); ##STR00001##
wherein; n is integer from 1 to 8; R.sup.1 and R.sup.2 independently represents group selected from alkyl, alkenyl, alkynyl, phenyl, or benzyl groups; and X represents group selected from hydroxy or amine. The coalescing agent according to this invention contains low amount of volatile organic compounds, has no pungent odour, and environmental friendly. Moreover, it provides good efficacy when being used as coating component.

Claims

1. A coalescing agent as represented in structure (I); ##STR00006## wherein; n is integer from 1 to 8; R.sup.1 and R.sup.2 are independently selected from alkyl, alkenyl, alkynyl, phenyl, or benzyl groups; and X is selected from hydroxy or amine.

2. The coalescing agent according to claim 1, wherein n is integer from 1 to 4.

3. The coalescing agent according to claim 1, wherein R.sup.1 and R.sup.2 are independently selected from linear alkyl group having 1 to 4 carbon atoms.

4. The coalescing agent according to claim 1, wherein X is hydroxy group.

5. The coalescing agent according to claim 1, wherein said coalescing agent is prepared from a reaction between a diacid compound selected from malonic acid, malonic anhydride, succinic acid, succinic anhydride, glutaric acid, glutaric anhydride, adipic acid, adipic anhydride, or mixtures thereof; a monoalcohol compound selected from methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, isobutanol, tert-butanol, or mixtures thereof; and a dialcohol compound selected from propylene glycol, 1,2-butanediol, 1,2-pentanediol, 1,2-hexanediol, 1,2-heptanediol, 1,2-octanediol, or mixtures thereof.

6. The coalescing agent according to claim 1, wherein the coalescing agent is ethyl 2-hydroxypropyl succinate.

7. A coating composition, comprising: a) at least one coalescing agent as represented in structure (I); ##STR00007## wherein; n is integer from 1 to 8; R.sup.1 and R.sup.2 are independently selected from alkyl, alkenyl, alkynyl, phenyl, or benzyl groups; and X is selected from hydroxy or amine b) binder; and c) solvent.

8. The coating composition according to claim 7, wherein n is integer from 1 to 4.

9. The coating composition according to claim 7, wherein R.sup.1 and R.sup.2 are independently selected from linear alkyl group with 1 to 4 carbon atoms.

10. The coating composition according to claim 7, wherein X is hydroxy group.

11. The coating composition according to claim 7, wherein said coalescing agent is prepared from a reaction between a diacid compound selected from malonic acid, malonic anhydride, succinic acid, succinic anhydride, glutaric acid, glutaric anhydride, adipic acid, adipic anhydride, or mixtures thereof; a monoalcohol compound selected from methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, isobutanol, tert-butanol, or mixtures thereof; and a dialcohol compound selected from propylene glycol, 1,2-butanediol, 1,2-pentanediol, 1,2-hexanediol, 1,2-heptanediol, 1,2-octanediol, or mixtures thereof.

12. The coating composition according to claim 7, wherein the coalescing agent is ethyl 2-hydroxypropyl succinate.

13. The coating composition according to claim 7, wherein the amount of coalescing agent is in the range from 3 to 8% by weight and wherein the amount of binder is in the range from 45 to 75% by weight.

14. The coating composition according to claim 7, wherein said binder is selected from alkyd, acrylic, vinyl-acrylic, vinyl acetate/ethylene, polyurethane, epoxy, styrenic, styrenic-acrylic copolymer, styrene alkene copolymer groups, derivatives thereof, or mixtures thereof.

15. The coating composition according to claim 7, wherein said solvent is selected from water, alcohol, petroleum distillate, ester, glycol, glycol ether, or mixtures thereof.

16. The coating composition according to claim 7, wherein the coating composition further comprises an additive selected from pigment, pigment extender, colorant, surfactant, rheology modifier, texturing agent, defoamer, biocide, wetting agent, dispersing agent, crosslinker, thickener, antifreezing agent, stabilizer, or mixtures thereof.

Description

DESCRIPTION OF THE INVENTION

(1) The present invention relates to the coalescing agent and the coating composition containing said coalescing agent which will be described according to the following embodiments.

(2) Therefore, any embodiment shown here means including its application to other embodiments of this invention unless stated otherwise.

Definitions

(3) Technical terms or scientific terms used herein have definitions which will be understood by ordinary person skilled in the art unless stated otherwise.

(4) Any instruments, apparatus, methods, or chemicals named herein mean instruments, apparatus, methods, or chemicals being used generally by person skilled in the art unless stated otherwise that they are instruments, apparatus, methods, or chemicals specific only in this invention.

(5) Use of singular nouns or singular pronouns with comprising in claims or specification means one and including one or more, at least one, and one or more than one.

(6) All compositions and/or methods disclosed and claimed in this application are intended to cover embodiments from any operation, performance, modification, or adjustment any factors without any experiment that significantly different from this invention, and obtain with object with utility and resulted as same as the present embodiment according to person ordinary skilled in the art although without specifically stated in claims. Therefore, substitutable or similar object to the present embodiment, including any minor modification or adjustment that can be apparent to person skilled in the art should be construed as remains in spirit, scope, and concept of invention as appeared in appended claims.

(7) Throughout this application, term about means any number that appeared or expressed herein that could be varied or deviated from any error of instruments, apparatus, method, or personal using said instruments, apparatus or method.

(8) Hereafter, invention embodiments are shown without any purpose to limit any scope of the invention.

(9) This invention relates to the coalescing agent as represented in structure (I);

(10) ##STR00003##

(11) wherein;

(12) n is integer from 1 to 8;

(13) R.sup.1 and R.sup.2 are independently selected from alkyl, alkenyl, alkynyl, phenyl, or benzyl groups; and

(14) X is selected from hydroxy or amine.

(15) Preferable, n is integer from 1 to 4. Most preferable, n is integer of 2.

(16) Preferable, R.sup.1 and R.sup.2 are independently selected from linear alkyl group having 1 to 4 carbon atoms. More preferable, R.sup.1 is ethyl group and R.sup.2 is methyl group.

(17) Preferable, x is hydroxy group.

(18) In one embodiment, the coalescing agent according to structure (I) is prepared from reaction between diacid compound and monoalcohol compound and dialcohol compound.

(19) Said diacid compound may be selected from malonic acid, malonic anhydride, succinic acid, succinic anhydride, glutaric acid, glutaric anhydride, adipic acid, adipic anhydride, pimelic acid, pimelic anhydride, suberic acid, suberic anhydride, azelaic acid, azelaic anhydride, sebacic acid, sebacic anhydride, or mixture thereof.

(20) Preferable, the diacid compound may be selected from malonic acid, malonic anhydride, succinic acid, succinic anhydride, glutaric acid, glutaric anhydride, adipic acid, adipic anhydride, or mixture thereof. Most preferable, the diacid compound is selected from succinic acid, succinic anhydride, or mixture thereof.

(21) In one embodiment, the monoalcohol compound may be selected from methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, isobutanol, tert-butanol, or mixture thereof.

(22) Preferable, the monoalcohol compound is ethanol.

(23) In one embodiment, the dialcohol compound may be selected from propylene glycol, 1,2-butanediol, 1,2-pentanediol, 1,2-hexanediol, 1,2-heptanediol, 1,2-octanediol, or mixture thereof.

(24) Preferable, the dialcohol compound is propylene glycol.

(25) In suitable embodiment according to the invention, when n is 2, R.sup.1 is selected from ethyl group, R.sup.2 is selected from methyl group, and X is selected from hydroxy group, the coalescing agent according to this invention is ethyl 2-hydroxypropyl succinate according to structure (II)

(26) ##STR00004##

(27) Another objective of this invention is the coating composition, comprising:

(28) a) at least one coalescing agent as represented in structure (I);

(29) ##STR00005##

(30) wherein;

(31) n is integer from 1 to 8;

(32) R.sup.1 and R.sup.2 are independently selected from alkyl, alkenyl, alkynyl, phenyl, or benzyl groups; and

(33) X is selected from hydroxy or amine

(34) b) binder; and

(35) c) solvent.

(36) The embodiments and the preferable embodiments of the coalescing agent in a) are as described previously.

(37) In one embodiment, the amount of coalescing agent in a) is in the range from 1 to 20% by weight, preferable is 3 to 8% by weight.

(38) The binder in b) may be selected from alkyd, acrylic, vinyl-acrylic, vinyl acetate/ethylene, polyurethane, epoxy, styrenic, styrenic-acrylic copolymer, styrene alkene copolymer, derivatives thereof, or mixture thereof.

(39) Preferable, said binder is selected from acrylic, styrenic-acrylic copolymer, or mixture thereof.

(40) In one embodiment, the amount of binder is in the range from 10 to 80% by weight, preferable is 45 to 75% by weight.

(41) In one embodiment, the solvent in b) may be selected from solvent compatible with the coalescing agent, wherein said solvent may be selected from water, alcohol, petroleum distillate, ester, glycol, glycol ether, or mixture thereof.

(42) In one optional embodiment, the coating composition may further comprising of pigment, pigment extender, colorant, surfactant, rheology modifier, texturing agent, defoamer, biocide, wetting agent, dispersing agent, crosslinker, thickener, antifreezing agent, stabilizer, or mixture thereof.

(43) Also in one optional embodiment, the coating composition may further comprising of additional coalescing agent, wherein the additional coalescing agent may be selected from benzoate ester, ester-alcohol, glycol-ether, long chain aliphatic alcohol, aromatic alcohol, or mixture thereof.

(44) The following is example which is only one embodiment of this invention and not intended to be limitation of this invention in any way.

(45) The Preparation of Diester Derivative to be Used as the Coalescing Agent

(46) The diester derivative which is used as the coalescing agent for the coating agent formulation can be prepared according to the following process.

(47) The Preparation of the Coalescing Agent Ethyl 2-Hydroxypropyl Succinate (COA-1)

(48) In the preparation of the coalescing agent COA-1, 1.0 mole succinic anhydride and 5.0 moles ethanol were added into round bottom flask and refluxed at 80 C. for 24 hours. Then, the excess ethanol of the reaction was distilled out and obtained product was extracted with the mixed solvent comprising dichloromethane and water. Then, dichloromethane layer was evaporated to obtain monoethyl succinate of the further reactions.

(49) One mole monoethyl succinate obtained from the first step and 1.2 moles propylene glycol were added into round bottom flask and refluxed at 110 C. for 12 hours by using p-toluene sulfonic acid (1% by weight of succinic anhydride) as a catalyst. Then, solvent was evaporated from the system and extracted with dichloromethane. Sodium hydrogen carbonate was added into the product after extraction. Then, dichloromethane layer was evaporated to obtain COA-1 product which was further analyzed for its characteristics.

(50) The Preparation of the Coalescing Agent Ethyl 2-Hydroxypropyl Succinate (COA-2)

(51) The preparation of the coalescing agent COA-2 can be prepared by the same process as for the preparation of COA-1 but isopropanol was used instead of ethanol as alcohol in the first step.

(52) The Preparation of the Coalescing Agent Ethyl Methyl Succinate (COA-3)

(53) In the preparation of the coalescing agent COA-3, 1.0 mole succinic anhydride and 5.0 moles ethanol were added into round bottom flask and refluxed at 80 C. for 24 hours. Then, the excess ethanol of the reaction was distilled out and the obtained product was extracted with the mixed solvent comprising dichloromethane and water. Then, dichloromethane layer was evaporated to obtain monoethyl succinate of the further reactions.

(54) One mole monoethyl succinate obtained from the first step and 5.0 moles methanol were added into round bottom flask and refluxed at 110 C. for 12 hours by using p-toluene sulfonic acid (1% by weight of succinic anhydride) as catalyst. Then, residual precursors from the reaction and solvent were evaporated and extracted with dichloromethane. Sodium hydrogen carbonate was added into the product after extraction. Then, dichloromethane layer was evaporated to obtain COA-3 product which was further analyzed for its characteristics.

(55) The Preparation of the Coalescing Agent Dimethyl Succinate (COA-4)

(56) In the preparation of the coalescing agent COA-4, 1.0 mole succinic anhydride and 6.0 moles ethanol were added in to round bottom flask with a solvent of toluene. Then, the mixture was refluxed at 110 C. for 24 hours by using p-toluene sulfonic acid (1% by weight of succinic anhydride) as catalyst. Then, residual precursors from the reaction and solvent were evaporated and extracted with dichloromethane. Sodium hydrogen carbonate was added into the product after extraction. Then, dichloromethane layer was evaporated to obtain COA-4 product which was further analyzed for its characteristics.

(57) The Preparation of the Coalescing Agent Dibutyl Succinate (COA-5)

(58) The preparation of the coalescing agent COA-5 can be prepared by the same process as for the preparation of COA-4 but isopropanol was used instead of butanol as alcohol in the first step.

(59) Properties Testing of Diester Derivatives

(60) The said obtained diester derivatives were analyzed by the following methods.

(61) Film Forming Efficacy

(62) The film forming efficacy of the coalescing agent COA-1 to COA-5 comparing to the commercial coalescing agent Texanol and Butyl Cellosolve can be performed according to the following steps.

(63) 1. 20 g of binders (acrylic or copolymer of styrenic-acrylic) were added into testing beaker.

(64) 2. 1-15% by weight of the tested coalescing agent from COA-1 to COA-5 was slowly added during stirred until the coalescing agent was homogeneously mixed with the binder. This took about 10-15 mins in order to complete the each concentration of 1-15% of coalescing agent that had been prepared.

(65) 3. The prepared coalescing agent and the binder obtained from 2 were drawn onto supporting paper using wire coater until 100 micron thick film layer was obtained. Then, the obtained film was left to be dried at room temperature.

(66) 4. When the film was dry, appearance of film was observed. The film must be transparent and not broken. Then, percentage of the coalescing agent capable to produce good film was recorded.

(67) Drying Property

(68) The drying property of the coalescing agent COA-1 to COA-5 comparing to the commercial coalescing agent Texanol and Butyl Cellosolve can be performed according to the following steps.

(69) 1. 20 g of binder selected from acrylic or copolymer of styrenic-acrylic and the amount of the coalescing agent COA-1 to COA-5 capable to produce the best film were added into testing beaker. The mixture was mixed and stirred until homogeneously mixed.

(70) 2. The prepared coalescing agent and binder obtained from 1 were drawn onto supporting paper using wire coater until 100 micron thick film layer was obtained. Then, the obtained film was left to be dried at room temperature.

(71) 3. The prepared film was touch by finger. The time that there was no fingerprint shown on the film was recorded.

(72) Odour Testing

(73) The odour testing of the coalescing agent COA-1 to COA-5 comparing to the commercial coalescing agent Texanol and Butyl Cellosolve can be performed according to the following steps.

(74) 1. 10 g of the coalescing agent COA-1 to COA-5 were added into each testing beaker.

(75) 2. Five assessors were asked to smell and recorded the odour intensity from 0-3, wherein 3 meant highest odour intensity and 0 meant no odour detected.

(76) Volatile Organic Compound (VOC) Testing

(77) The testing of VOC of the coalescing agent COA-1 to COA-5 comparing to the commercial coalescing agent Texanol and Butyl Cellosolve can be performed according to the ISO 11890-2 standard.

(78) The Properties of the Coalescing Agent

(79) The properties of the coalescing agent COA-1 to COA-5 comparing to the commercial coalescing agent Texanol and Butyl Cellosolve is shown in table 1. From the tests, it can be seen that the coalescing agent COA-1 and COA-2 according to the present invention has the same level of the film forming efficacy as those commercial coalescing agents. These coalescing agents according to the present invention need only 6% by weight in order to produce film as same as those commercial coalescing agents. On the other hand, the rest of coalescing agents, which are alkyl succinate esters of COA-3, COA-4, and COA-5, are not able to form polymer film of binders. Moreover, the coalescing agent according to the present invention need similar drying time as those commercial coalescing agents. The coalescing agent according to the present invention has less odour intensity than those commercial coalescing agents. This shows that the coalescing agent according to the present invention has similar efficacy as those commercial coalescing agents but has less odour intensity and lower amount of volatile organic compound.

(80) TABLE-US-00001 TABLE 1 Properties of the coalescing agent according to the present invention comparing to the commercial coalescing agents Acrylic Binder Copolymer of Styrenic-Acrylic Binder Amount used Drying Amount used Drying to form film Film of film to form film Film of film VOC Sample (% by weight) characteristic (min) Odour (% by weight) characteristic (min) Odour (g/l) Texanol 5 transparent 28 3 5 transparent 20 3 4.48 Butyl Cellosolve 9 transparent 25 3 6 transparent 20 3 4.98 COA-1 6 transparent 27 1 5 transparent 20 1 1.27 COA-2 6 transparent 26.5 1 6 transparent 20 1 1.25 COA-3 film cannot film cannot be formed be formed COA-4 film cannot film cannot be formed be formed COA-5 film cannot film cannot be formed be formed

BEST MODE OR PREFERRED EMBODIMENT OF THE INVENTION

(81) Best mode or preferred embodiment of the invention is as provided in the description of the invention.