Replacement plasticizer system for phthalate-plasticized formulations

Information

  • Patent Grant
  • 8557139
  • Patent Number
    8,557,139
  • Date Filed
    Thursday, February 12, 2009
    15 years ago
  • Date Issued
    Tuesday, October 15, 2013
    11 years ago
Abstract
The present invention is a replacement plasticizer system made from or containing an epoxidized fatty acid ester plasticizer as a primary plasticizer and a secondary plasticizer. The replacement placement system is useful with a variety of polymers in applications such as wire-and-cable insulations, wire-and-cable jackets, coatings, adhesives, and castings.
Description

The present invention generally relates to the field of polymers. Specifically, the present invention relates to plasticizers used in polymers to create desired physical characteristics in the resulting polymer/plasticizer complex, such as increasing flexibility, pliability, and plasticity in the resultant polymer complex,


For example, plasticizers such as di(2-ethythexyl)phthalate (“DEHP”), di-isononyl phthalate (“DINP”), and other phthalate plasticizers have long been industry standard plasticizers used with polymers such as homo- and copolymers- of polyvinyl chloride (“PVC”), polyvinyl dichlorides (“PVDC”), vinyls, and similar polymers and resins to impart pliability and plasticity while retaining good tensile strength and resistance to cracking at low temperatures. For example, phthalate plasticizers have been used with rigid polymers such as PVC to create pliable materials used in such goods as intravenous (IV) bags and tubing, molded children's toys that require a soft or malleable feel, and various other applications where pliability or softness needs to be imparted to a polymer.


Phthalate plasticizers such as DEHP and DINP were once preferred plasticizers due to their ability to impart the physical characteristics noted above, and their permanence in the polymer over time, even when exposed to relatively high temperatures and humidity. However, public sentiment has prompted many manufacturers of consumer products to discontinue use of phthalates as a plasticizer due to concerns over potential adverse health effects, Thus, plasticizer compositions that reduce or eliminate phthalates, but perform similarly to DINP or other effective phthalate plasticizers, would be greatly appreciated in the art. Moreover, alternative non-phthalate plasticizers, which show an improved permanence in, and high compatibility with, a broad range of polymers would be greatly appreciated in the art.


Notable phthalate-free examples of plasticizers for use in PVC formulations include epoxidized soy oil. Unfortunately, epoxidized soy oil has limited solubility in PVC and insufficiently plasticizes PVC for many applications. Other epoxides have been identified as potential PVC plasticizers, including epoxies made from esters of fatty acids, the epoxy of 2-ethylhexyanol, and epoxidized palm oil esters. Unfortunately, epoxides made from esters of fatty acids such as the epoxidized methyl ester of soy oil are too volatile to serve as useful plasticizers of PVC.


Yet, the need exists for phthalate-free plasticizers that are compatible with other plasticizers, suitably nonvolatile, not petroleum-based, and capable of imparting thermal stability to formulations presently using phthalate plasticizers. It is further desirable to broaden the applications in which PVC, other halogenated polymers, acid-functionalized polymers, anhydride-functionalized polymers, and nitrile rubbers may be used by developing new plasticized formulations. In some instances, it might prove useful for the plasticizer or the plasticizer system to act as an acid scavenger.


To that end, the presently invented replacement plasticizer system is provided, comprising an epoxidized fatty acid ester plasticizer as a primary plasticizer and a secondary plasticizer. The replacement placement system is useful with a variety of polymers in applications such as wire-and-cable insulations, wire-and-cable jackets, coatings, adhesives, and castings.


Suitable epoxidized fatty acid ester plasticizers include epoxidized biodiesel and epoxidized derivatives of fatty acid esters of biodiesel. For the purposes of this application, the term “biodiesel” means herein mono-alkyl esters of long chain fatty acids derived from vegetable oils or animal fats. Preferably, the biodiesel is derived from vegetable oils.


Also, preferably, the epoxidized fatty acid ester is an epoxide of a fatty acid methyl ester. More generally, the epoxidized fatty acid ester can be any epoxidized fatty acid C1-C14 ester, including ethyl, propyl, butyl, and 2-ethylhexyl esters.


The epoxidized fatty acid ester can be prepared in a variety of conventional ways. For example, natural oils can be used as the starting material. In that instance, the natural oils can be saponified to the fatty acids and then esterified with alcohols. Next, the low molecular weight esters are epoxidized. The unsaturated ester can be epoxidized with a per-acid.


Alternatively, a glycidyl ester of the fatty acid can be prepared via epichlorohydrin or related chemicals. In yet another alternate, it is possible to transesterify the triglyceride with alcohols and then epoxidize the unsaturated fatty ester with a per-acid.


An example of preparing an epoxide of a fatty acid methyl ester begins with soy oil, wherein the soy oil is transesterified with methanol to make the methyl ester of the fatty acids in the oil. Glycerol is removed from the reaction products due to insolubility. A solution of per acetic acid in ethyl acetate is used to epoxidize the double bonds on the fatty acids. The per-acid is kept below 35% per acid and 35 degrees Celsius to prevent detonation. After completion, the ethyl acetate and product acetic acid are removed via vacuum stripping.


When formulated with the polymer, the primary plasticizer is present in an amount of from about 0.1 to about 60 parts per hundred rubber.


Suitable secondary plasticizers include any plasticizer having a vapor pressure lower than that of the epoxidized fatty acid ester. For example, when the epoxidized fatty acid ester is an epoxide of a fatty acid methyl ester, a suitable secondary plasticizer is preferably epoxidized soy oil. Secondary plasticizers include epoxidized soy oil, epoxidized linseed oil, and epoxides of other vegetable oils as well as conventional plasticizers such as petroleum-based phthalates, chlorinated hydrocarbons, trimelitates, and phosphate-based plasticizers. Notably, when flame retardancy is desirable, a phosphate plasticizer is suitable.


Preferably, the secondary plasticizer is not a phthalate. As such, preferably, the replacement placement system is phthalate-free.


When formulated with the polymer, the second plasticizer is present in an amount of from about 0.1 to about 60 parts per hundred rubber. Preferably, the primary and secondary plasticizers are present in a 1:1 ratio.


Suitable polymers for using the replacement plasticizer system of the present invention include halogenated polymers, acid-functionalized polymers, anhydride-functionalized polymers, and nitrile rubbers. Preferably, the polymer is a halogenated polymer. More preferably, the halogenated polymer is a PVC polymer selected from the group consisting of PVC homopolymers, PVC copolymers, polyvinyl dichlorides (PVDC), and polymers of vinylchloride with vinyl, acrylic and other co-monomers. Examples of other suitable halogenated polymers are chlorinated polyolefins and chlorinated rubbers.


Suitable acid-functionalized polymers include acrylic-acid functionalized polymers. Notably, the system is also useful with acrylic and other polymers that require plasticizers to reduce glass transitions or improve toughness.


The formulation may further comprise fillers, pigments, metal ion containing stabilizers, UV stabilizers, lubricants, metal soaps, oxides of stabilizers, additional plasticizers, and processing aids.







EXAMPLES

The following non-limiting examples illustrate the invention.


Example 1 and Comparative Example 2

A simplified PVC wire insulation formulation was produced with a primary and a secondary plasticizer. The PVC used was Oxychem 240F polyvinyl chloride homopolymer, having a K Value of 70. The calcium carbonate was obtained from Huber Materials. The dibutyl tin dilaurate (DBTDL) was obtained from Arkema. The epoxidized soy oil was obtained from Ferro Corp.


The comparative example was prepared using diisodecyl phthalate (DIDP), a conventional plasticizer, as the primary plasticizer and was obtained from VWR International. The example of the present invention was prepared with epoxidized biodiesel as the primary plasticizer.


The amount of each component is shown based on parts per hundred rubber (phr).


The target glass transition temperature (Tg) was 40-50 degrees Celsius.











TABLE 1





Component
Example 1
Comp. Ex. 2

















PVC
100
100


DIDP

40


epoxidized biodiesel
28


CaCO3
10
10


DBTDL
4
4


Epoxidized soy oil
2
2







Physical Properties









Tg
42 degrees Celsius
42 degrees Celsius









Example 3 and Comparative Example 4

A simplified PVC electrical cable jacket formulation was produced. The PVC was Oxychem 240F polyvinyl chloride homopolymer, having a K Value of 70. The calcium carbonate was obtained from Huber Materials. A Zn/Ca stabilizer was obtained as MARK™ 6797 Zn/Ca stabilizer from Chemtura Corporation. The antioxidant was IRGANOX™ 1076 monofunctional hindered phenolic antioxidant available from Ciba Corporation. The epoxidized soy oil was obtained from Ferro Corp. The amount of each component is shown based on parts per hundred rubber (phr).


For the aging evaluation, the test specimen of each formulation was subjected to 100 degrees Celsius for 10 days. To achieve desired industry performance, a minimum of 65% retention of the initial elongation is required.













TABLE 2







Component
Example 3
Comp. Ex. 4




















PVC
100
100



epoxidized biodiesel
27.5
55



epoxidized soy oil
27.5



CaCO3
68
68



Zn/Ca stabilizer
2.5
2.5



Antioxidant
0.05
0.05







Physical Properties











Shore A
85
75



Strain at Break (initial)
260%
400%



Strain at Break (aged)
180%
200%



% Elongation Retained
 73%
 50%









Claims
  • 1. A plasticizer system composition comprising: (a) a primary plasticizer consisting of an epoxidized fatty acid ester plasticizer selected from the group consisting of epoxidized biodiesel, epoxidized derivatives of fatty acid esters of biodiesel and an epoxide of a fatty acid methyl ester, and(b) a secondary plasticizer selected from the group consisting of epoxidized soy oil, epoxidized linseed oil, and epoxides of other vegetable oils,wherein the system is phthalate free.
  • 2. The plasticizer system composition of claim 1 wherein the biodiesel is derived from a vegetable oil.
  • 3. A plasticized polymer composition comprising: (a) a polymer selected from the group consisting of halogenated polymers, acid-functionalized polymers, anhydride-functionalized polymers, and nitrile rubbers; and(b) a plasticizer system according to any of claims 1 or 2.
  • 4. The plasticized polymer composition of claim 3 wherein the polymer is a polyvinyl chloride polymer (PVC) selected from the group consisting of PVC homopolymers, PVC copolymers, polyvinyl dichlorides (PVDC), and polymers of vinylchloride with vinyl, acrylic and other co-monomers.
  • 5. A cable comprising one or more electrical conductors or a core of one or more electrical conductors, each conductor or core being surrounded by a layer comprising the plasticized polymer composition according to either of claims 3 or 4.
  • 6. The plasticizer system composition of claim 1 wherein the secondary plasticizer is epoxidized soy oil.
  • 7. The plasticizer system composition of claim 1 wherein the primary plasticizer and the secondary plasticizer are present in approximately a 1:1 weight ratio.
PCT Information
Filing Document Filing Date Country Kind 371c Date
PCT/US2009/033935 2/12/2009 WO 00 8/6/2010
Publishing Document Publishing Date Country Kind
WO2009/102877 8/20/2009 WO A
US Referenced Citations (75)
Number Name Date Kind
2397592 Blades Apr 1946 A
2403215 Foster Jul 1946 A
2458484 Terry et al. Jan 1949 A
2500918 Rueter et al. Mar 1950 A
2618622 Grummit et al. Nov 1952 A
2666752 Grummit et al. Jan 1954 A
3138566 Arnold Jun 1964 A
3281382 Kuester et al. Oct 1966 A
3409580 Alzner Nov 1968 A
3639318 Tijunelis et al. Feb 1972 A
3668091 French et al. Jun 1972 A
3712875 Tijunelis Jan 1973 A
3778465 Barnstorf Dec 1973 A
3780140 Hammer Dec 1973 A
3868341 Sauer et al. Feb 1975 A
3872187 Fath Mar 1975 A
3891694 Mills et al. Jun 1975 A
4083816 Frankel et al. Apr 1978 A
4346145 Choi et al. Aug 1982 A
4421886 Worschech et al. Dec 1983 A
4426477 Yasumatsu et al. Jan 1984 A
4556694 Wallace Dec 1985 A
4605694 Walker Aug 1986 A
4612192 Scheuffgen et al. Sep 1986 A
4613533 Loomis et al. Sep 1986 A
4627993 Loomis Dec 1986 A
4670494 Semenza, Jr. Jun 1987 A
4857600 Gross et al. Aug 1989 A
5225108 Bae et al. Jul 1993 A
5227417 Kroushl, III Jul 1993 A
5246783 Spenadel et al. Sep 1993 A
5270366 Hein Dec 1993 A
5278236 Case et al. Jan 1994 A
5430108 Schlosberg et al. Jul 1995 A
5454806 Shinonome Oct 1995 A
5464903 Hofmann Nov 1995 A
5466267 Baillargeon et al. Nov 1995 A
5575965 Caronia et al. Nov 1996 A
5736605 Oshima Apr 1998 A
5756570 Hoch et al. May 1998 A
5886072 Linsky et al. Mar 1999 A
6063846 Weng et al. May 2000 A
6114425 Day et al. Sep 2000 A
6274750 Sato et al. Aug 2001 B1
6417260 Weng et al. Jul 2002 B1
6437170 Thil et al. Aug 2002 B1
6451958 Fan et al. Sep 2002 B1
6495033 Talboom Dec 2002 B1
6496629 Ma et al. Dec 2002 B2
6608142 Weng et al. Aug 2003 B1
6706815 Marchand et al. Mar 2004 B2
6714707 Rossi et al. Mar 2004 B2
6734241 Nielsen et al. May 2004 B1
6797753 Benecke et al. Sep 2004 B2
6849694 Hata Feb 2005 B2
6949597 Nielsen et al. Sep 2005 B2
7700675 Bueno de Almeida et al. Apr 2010 B2
20020013396 Benecke et al. Jan 2002 A1
20040122159 Mhetar et al. Jun 2004 A1
20050090590 Nielsen et al. Apr 2005 A1
20050203230 Kadakia et al. Sep 2005 A1
20060025544 Koube et al. Feb 2006 A1
20060276575 Hamaguchi et al. Dec 2006 A1
20070100049 Ishizuka May 2007 A1
20070135562 Freese et al. Jun 2007 A1
20080200595 Hinault et al. Aug 2008 A1
20080227993 Zuckerman Sep 2008 A1
20090149585 De Quadros, Jr. et al. Jun 2009 A1
20090149586 De Quadros, Jr. et al. Jun 2009 A1
20090312478 Hasegawa et al. Dec 2009 A1
20100010127 Barki et al. Jan 2010 A1
20100256278 Harada et al. Oct 2010 A1
20110076502 Chaudhary et al. Mar 2011 A1
20110272174 Chaudhary Nov 2011 A1
20130005937 Cramail et al. Jan 2013 A1
Foreign Referenced Citations (52)
Number Date Country
1188445 Jun 1985 CA
1341681 Mar 2002 CN
10107510 Nov 2007 CN
101108982 Jan 2008 CN
101108982 Jan 2008 CN
101591588 Dec 2009 CN
101824193 Sep 2010 CN
101914219 Dec 2010 CN
0192961 Sep 1986 EP
0358179 Mar 1990 EP
0364717 Apr 1990 EP
0 393 813 Oct 1990 EP
0473915 Mar 1992 EP
0565984 Oct 1993 EP
0986606 Mar 2000 EP
1218443 Jul 2002 EP
1361039 Nov 2003 EP
1624014 Feb 2006 EP
2070977 Jun 2009 EP
1437722 May 1966 FR
499931 Jan 1939 GB
790314 Feb 1958 GB
910543 Nov 1962 GB
934689 Aug 1963 GB
1022920 Mar 1966 GB
1102506 Feb 1968 GB
1341623 Dec 1973 GB
2155021 Sep 1985 GB
S44-007131 Mar 1969 JP
S61-016950 Jan 1986 JP
04-059851 Feb 1992 JP
H04-085354 Mar 1992 JP
H04-261452 Sep 1992 JP
2000-319468 Nov 2000 JP
2003-064233 Mar 2003 JP
2003-297149 Oct 2003 JP
2004311064 Nov 2004 JP
2010-042669 Feb 2010 JP
9730115 Aug 1997 WO
0114466 Mar 2001 WO
0198404 Dec 2001 WO
2004052977 Jun 2004 WO
2007006489 Jan 2007 WO
WO-2007006489 Jan 2007 WO
2008081330 Jul 2008 WO
2008081332 Jul 2008 WO
2008122364 Oct 2008 WO
2009102877 Aug 2009 WO
2011041372 Apr 2011 WO
2011041380 Apr 2011 WO
2011041388 Apr 2011 WO
2013003225 Jan 2013 WO
Non-Patent Literature Citations (45)
Entry
Gan, L.H., et al (1994). Epoxidized esters of palm olein as plasticizers for poly(vinyl chloride). European Polymer Journal, 31(8), 7i9-724.
Greenspan, F.P., el al (1953). Epoxy fatty acid ester plasticizers. Industrial and Engineering Chemistry, 45(12), 2722-2726.
Bizzari, S.N., et al (2003). Plasticizers. C E H Marketing Research Report, 38-64, Retrieved from http://www.sriconsulting.com.
Greenspan, F.P., et al (1956). Epoxy fatty acid ester plasticizers. Preparation and properties. The Journal of the American Oil Chemists' Society, 33, 391-394.
Gan, L.H., et al (1994). Epoxidized esters of palm olein as plasticizers for poly(vinyl chloride). European Polymer Journal, 31(8), 719-724.
Greenspan, F.P., et al (1953). Epoxy fatty acid ester plasticizers. Industrial and Engineering Chemistry, 45(12), 2722-2726.
Bizzari, S.N., et al (2003). Plasticizers. CEH Marketing Research Report, 38-39,42,52. Retrieved from http://www.sriconsulting.com.
Barnicoat, C.R. 1945. Reactions and properties of annatto as a cheese colour. Part II. J. Dairy Res. 14: 59-63.
Campanella A. et al.; High Yield Epoxidation of Fatty Acid Methyl Esters with Performic Acid Generated In Situ; Chemical Engineering Journal, 144 (2008) 466-475 (Elsevier B.V.).
Chuanshang Cai, et al.; Studies on the Kinetics of In Situ Epoxidation of Vegetable Oils; Eur. J. Lipid Sci. Technol., 2008, 110, 341-346 (Wiley-VCH GmbH & Co. KGaA, Weinheim).
Corrigan, Brian, Oil purification, filtration and reclamation, Iron Age (1947) 159(14).
Du G., et al., Catalytic Epoxidation of Methyl Linoleate, JAOCS, vol. 81, No. 4 (2004).
Freedman, F., Butterfield, R., and Pryde, E.H. Transesterification Kinetics of Soybean Oil. JAOCS, 63(10) p. 1375 (1986).
Grummitt O. and Fleming H. Acetylated Castor Oil Industrial and Engineering Chemistry, vol. 37, No. 5, May 1945, pp. 485-491.
Haas, Michael J. Improving the Economics of biodiesel production through the use of low value lipids as feedstocks: vegetable oil soapstock, Fuel Processing Technology 86 p. 1087-96 (2005).
Jensen, R.G. Purification of Triglycerides with an Aluminca Column, Lipids, 451-452 (1966).
Morgenstern, B. “Epoxidized Fatty Acid Esters as Plasticizers for PVC” dated Apr. 22, 2005.
Morgenstern, B. Epoxidized Fatty Acid Esters as Plasticizers for PVC, presented at the 7th Freiberg Polymer Conference, Apr. 21 and 22, 2005.
Morgenstern, B. Use of Modified Fatty Acid Esters as Plasticizers for PVC, dated Sep. 12, 2003.
Opposition dated Jan. 9, 2013 EP2245089B1.
Orellana-Coca et al., Lipase Mediated Simultaneious Esterification and Epoxidation of Oleic Acid for the Production of Alkylepoxystearates. Journal of Molecular Catalysis B: Enzymatic 44 (2007) 133-137.
Stuart, A et al., Polym. Bull. (2010) 65:589-598.
Rehberg, C. et al. Plasticizers from Lactic Esters and Biabasic Acids Ind. Eng. Chem., 1952, 44 (9), pp. 2191-2195.
Santacesaria E. et al.; A Biphasic Model Describing Soybean Oil Epoxidation with H2O2 in a Fed-Batch Reactor; Chemical Engineering Journal, vol. 173, Issue 1, Sep. 1, 2011, pp. 198-209 (Elsevier B.V.).
Sen{hacek over (z)}ana S. et al.; Kinetics of In Situ Epoxidation of Soybean Oil in Bulk Catalyzed by Ion Exchange Resin; Journal of the American Oil Chemists' Society, vol. 78, No. 7 (2001) 725-731 (AOCS Press).
Sheehan, J et al. “A Look Back at the U.S. Department of Energy's Aquatic Species Program: Biodiesel from Algae”, National Renewable Energy Laboratory, Colorado, Jul. 1998, pp. 1-294.
Taylor, D. R. Proceedings of the World Conference on oilseed technology and utilization, Adsorptive Purification, American Oil Chemists Society, Champaing, 1992, p. 152-165.
Tekin A., and Hammond E. Factors Affecting the Electrical Resistivity of Soybean Oil, JAOCS, vol. 75(6) 1998.
XP002657062 Vertellus Performance Materials Inc.; Flexricin P-8 Technical Data Sheet, Nov. 2006.
XP002669860, Thomson Scientific, Mar. 13, 2009, London, GB.
TCI America, Online Catalog: Tributyrin; http://web.archive.org/web/20080511154307/http://www.tciamerica.com/.
PCT/US2010/050654 International Search Report and Written Opinion.
PCT/US2010/050676 International Search Report and Written Opinion.
PCT/US2010/050690 International Preliminary Report on Patentability.
PCT/US2010/050690 International Search Report and Written Opinion.
PCT/US2010/050699 International Search Report and Written Opinion.
PCT/US2011/035143 International Search Report and Written Opinion.
PCT/US2011/041557 International Preliminary Report on Patentability.
PCT/US2011/041557 International Search Report and Written Opinion.
PCT/US2011/045653 International Search Report and Written Opinion.
PCT/US2012/043740 International Search Report and Written Opinion.
PCT/US2012/055070 International Search Report and Written Opinion.
PCT/US2013/023362 International Search Report and Written Opinion.
PCT/US2009/033935 Internations Preliminary Report of Patentability.
PCT/US2009/033935 International Search Report and Written Opinion.
Related Publications (1)
Number Date Country
20120085568 A1 Apr 2012 US
Provisional Applications (1)
Number Date Country
61029035 Feb 2008 US