This application claims the benefit of PCT Application PCT/EP2008/007463 with International Filing Date of Sep. 11, 2008, published as WO 2009/036920 A1, which further claims priority to European Patent Application No. EP07075826.3 filed Sep. 20, 2007, the entire contents of both are hereby incorporated by reference.
The present invention relates to a method to prepare dimerized rosins dispersible in water in presence of extremely low level of dimerization acid catalyst. The present invention relates also to its use as a tackifier resin, solid or in water, and ink resin, and an adhesive composition and ink composition comprising the rosin resin.
Many methods for the dimerization of rosin have been published. Previous methods describe the use of strong inorganic acids, such as sulfuric acid as the catalyst, U.S. Pat. Nos. 2,136,525, 2,108,982, 2,307,641, 2,328,681, 2,515,218, 2,251,806, 2,532,120 and 4,105,462.
Alternative methods have been described using sulfonated polymers, U.S. Pat. No. 4,414,146, or a halogenated methanesulfonic acid, U.S. Pat. Nos. 4,339,377 and 4,172,070.
Further alternative methods describe the use of formic acid as the catalyst in U.S. Pat. Nos. 2,375,618, 2,492,146, 4,536,333.
The prior art uses processes including a final washing and catalyst removal step adding to the process complexity and cost.
It is an object of the present invention to provide a process that utilizes a catalyst that can be used at extremely low level and/or a catalyst that aids the subsequent product application thereby eliminating the need of a costly washing and catalyst removal step.
The present invention solves the above identified drawbacks by the use of a carboxylated sulfonic acids as catalyst to produce dimerized rosin. The process eliminates the need of catalyst removal by the high activity of the catalyst of the invention.
The present invention relates also to an adhesive composition comprising a dimerized rosin tackifier made according to the present method.
The present invention relates further to resins for ink application comprising the dimerized rosin as building block.
The present invention relates also to an ink composition comprising an ink resin based on the dimerized rosin.
The method of the invention to produce dimerized rosin is based on carboxylated sulfonic acids as catalyst. In one embodiment the carboxylated sulfonic acid derivatives like e.g. sulfosuccinic acid, 5-sulfosalicylic acid or 4-sulfophthalic acid are used as catalyst at 0.1 to 1 weight percent on rosin. In the preferred method 4-sulfosalicylic acid is used as catalyst. The catalyst can be left in the final product or optionally neutralized with alkali such as potassium hydroxide or amines.
The method of the invention to produce dimerized rosin, for subsequent application in water based dispersions such as water based tackifiers, is based on sulphonated surfactants as catalyst.
Production of water based dispersions such as water based tackifiers does require surfactants to aid the emulsification process and stabilize the final dispersion. Sulfonated surfactants are well known surfactants and widely used in many applications. In the embodiment process sulfonated surfactant is used as catalyst to produce dimerized rosin. The catalyst does not require a separation step and can be used at higher level of 1 to 5 weight percent on rosin, typical for the surfactant level in formulations to prepare water based tackifiers. In the subsequent emulsification process only alkali addition such as potassium hydroxide or amine is needed to produce a water based tackifier dispersion. The sulphonate surfactant fulfills a dual role. First as rosin dimerization catalyst then after a subsequent neutralization to form as emulsifier to prepare water based tackifier.
In the preferred embodiment of the present method dodecylbenzene sulfonic acid is used at about 3 weight percent. The process makes about 30% dimerized rosin. After neutralization with triethanol amine the subsequent tackifier dispersion is prepared.
After the addition of 1000 g Chinese gum rosin and 20 g 4-sulfophthalic acid at 135° C. in a glass reactor, the content is stirred and kept for 4 hours. Then the mixture is heated to 160° C. and kept for another 4 hours.
After the addition of 1000 g Chinese gum and 38 g dodecylbenzenesulfonic acid at 140° C. in a glass reactor, the content is stirred and kept for 4 hours.
The rosin resin of example 2, 1000 g, is molten at 110° C. in a steel beaker. While stirring, triethanolamine 25 g, is added. While stirring, water (60° C.) is added in 15 minutes time. The final dispersion is cooled.
Experiment using p-TSA (equimolar amount to 38 g dodecylbenzenesulfonate of example 2).
After the addition of 1000 g Tall oil rosin (TOR) and 20 g p-TSA at 135° C. in a glass reactor, the content is stirred and kept for 4 hours.
The temperature is increased to 150° C. and kept for another hour. 13 g KOH solution in water (50%) is added.
The rosin resin of example 4, 1000 g, is molten at 110° C. in a steel beaker. While stirring 1000 g water at 60° C. is added in 15 minutes time.
The content is cooled.
| Number | Date | Country | Kind |
|---|---|---|---|
| 07075826.3 | Sep 2007 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2008/007463 | 9/11/2008 | WO | 00 | 12/7/2010 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2009/036920 | 3/26/2009 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 1975211 | Johnston | Oct 1934 | A |
| 2011673 | Binapfl | Aug 1935 | A |
| 2288659 | Tyler | Jul 1942 | A |
| 2302632 | Humphrey | Nov 1942 | A |
| 2307641 | Rummelsburg | Jan 1943 | A |
| 2328681 | Rummelsburg | Sep 1943 | A |
| 2329566 | Tyler et al. | Sep 1943 | A |
| 2340696 | Rummelsburg | Feb 1944 | A |
| 2341239 | Percy et al. | Feb 1944 | A |
| 2375618 | Bried | May 1945 | A |
| 2419185 | Braidwood et al. | Apr 1947 | A |
| 3891612 | Parkin et al. | Jun 1975 | A |
| 3954690 | Hesse et al. | May 1976 | A |
| 4071375 | Ishibe et al. | Jan 1978 | A |
| 4157982 | Clemons et al. | Jun 1979 | A |
| 4199369 | Hughes et al. | Apr 1980 | A |
| 4263182 | Aldrich | Apr 1981 | A |
| 4339377 | Hollis | Jul 1982 | A |
| 4414146 | Olechowski et al. | Nov 1983 | A |
| 4536333 | Olechowski | Aug 1985 | A |
| 5021548 | Minn | Jun 1991 | A |
| 5175250 | Hazen | Dec 1992 | A |
| 6165320 | Bates et al. | Dec 2000 | A |
| 6369119 | Roberts et al. | Apr 2002 | B1 |
| 20030229178 | Locko et al. | Dec 2003 | A1 |
| 20040225076 | Martz et al. | Nov 2004 | A1 |
| 20050054801 | Locko et al. | Mar 2005 | A1 |
| 20050203228 | Aarts et al. | Sep 2005 | A1 |
| 20070141503 | Matsuoka et al. | Jun 2007 | A1 |
| 20070254985 | Maas et al. | Nov 2007 | A1 |
| 20080000389 | Locko et al. | Jan 2008 | A1 |
| Number | Date | Country |
|---|---|---|
| 1628159 | Jun 2005 | CN |
| 337733 | Oct 1930 | GB |
| 1474441 | May 1977 | GB |
| 342347 | Oct 1998 | TW |
| WO-03042308 | May 2003 | WO |
| WO 2005023948 | Mar 2005 | WO |
| Entry |
|---|
| Australian Examination Report issued in Australian Patent Application No. 2008300927 and dated Jan. 31, 2011. |
| European Communication issued in European Patent Application No. 08802024.3 and dated Sep. 9, 2010. |
| International Preliminary Report on Patentability issued in PCT/EP2008/007463 and dated Mar. 24, 2010. |
| International Search Report and Written Opinion issued in PCT/EP2008/007463 and mailed Jan. 22, 2009. |
| Office Action issued in Canadian Patent Application No. 2,700,043 and dated Mar. 30, 2012. |
| Office Action issued in Chinese Patent Application No. 200880170899.X and dated May 18, 2012 (English translation provided). |
| Office Action with Search Report received for Taiwan Application No. 097133645 dated Sep. 28, 2012 (8 pages)—English translation included. |
| Zinkel, Duane F. et al., “Naval Stores: Production-Chemistry-Utilization,” Pulp Chemicals Association, 1989, pp. 288, 585, and 704 (4 pages). |
| Search Report received for European Patent Application No. 12184851.9 dated Feb. 14, 2013 (6 pages). |
| Second Office Action issued in Chinese Patent Application No. 200880107899.X dated Mar. 4, 2013 (10 pages). |
| Stauffer, Don, “Distillations: Why is Rosin Polymerized,” Forest Chemicals Review, (Mar./Apr. 2002) (3 pages). |
| Number | Date | Country | |
|---|---|---|---|
| 20110092667 A1 | Apr 2011 | US |