|Publication number||USRE34904 E|
|Application number||US 08/086,872|
|Publication date||Apr 11, 1995|
|Filing date||Jul 8, 1993|
|Priority date||Oct 30, 1989|
|Also published as||CA2028387A1, EP0426086A1, US5120838|
|Publication number||08086872, 086872, US RE34904 E, US RE34904E, US-E-RE34904, USRE34904 E, USRE34904E|
|Inventors||Ernst K. Just, Thomas G. Majewicz, Arjun C. Sau|
|Original Assignee||Hercules Incorporated|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (65), Non-Patent Citations (3), Referenced by (11), Classifications (24), Legal Events (6)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This invention relates to a new class of modified water soluble polymers. Specifically it relates to alkylaryl hydrophobically modified hydroxyethylcellulose, methylcellulose and hydroxypropylcellulose.
Nonionic water soluble cellulose ethers are employed in a wide variety of industrial applications, as thickeners, as water retention aids, and as suspension aids in certain polymerization processes, among others. Widely used, commercially available, nonionic cellulose ethers include methylcellulose, hydroxypropylmethylcellulose, hydroxyethylcellulose, hydroxyethylpropylcellulose, hydroxypropylcellulose, and ethylhydroxyethylcellulose.
As is generally the case with high polymers, better thickening efficiency is realized with high molecular weigh cellulose ethers. U.S. Pat. Nos. 4,228,277 and 4,243,802 (Landoll) disclose nonionic cellulose ethers of relatively low molecular weight which are capable of producing viscous aqueous solutions in practical concentrations. U.S. Pat. No. 4,845,175 discloses alkylaryl hydrophobically modified hydroxyethylcellulose as a useful material for emulsion polymerization, but contains no disclosure of how to make or use the compounds of the present invention. These products exhibit a relatively high degree of surface activity compared to that of more conventional nonionic water soluble cellulose ethers. These products are nonionic cellulose ethers which are modified by substitution with specified amounts of C10 to C24 alkyl radicals. Such ethers are substituted with an amount of long chain alkyl hydrocarbon radical between about 0.2 weight percent and the amount which renders said cellulose ether less than 1% by weight soluble in water. The base cellulose ether thus modified is preferably one of low to medium molecular weight, i.e., less than about 800,000 and preferably between 20,000 and 500,000, or a Degree of Polymerization (D.P.) of about 75 to 1,800.
Modification of the cellulose ethers with small hydrophobic groups such as ethyl, benzyl and phenylhydroxyethyl groups were not found to effect the property improvements shown by the long chain alkyl hydrophobic modifications. The long chain alkyl cellulose ethers disclosed were useful as stabilizers in emulsion polymerizations, as thickeners in cosmetics, and as flocculants in mineral processing. One particularly good utility was as a thickener in latex paint, where very small amounts of low molecular weight long chain alkyl modified nonionic cellulose ethers outperformed larger quantities of higher molecular weight conventional nonionic cellulosic ethers. The advantages of these products in this particular use are discussed in detail in the Aqualon publication entitled "Natrosol® Plus-Modified Hydroxyethylcellulose-Performance as a Latex Paint Thickener," Specifically, they provide improved paint rheology, excellent spatter resistance, and good thickening efficiency in a wide variety of latex paint formulations. Paint leveling properties are adequate and better than those obtained with the unmodified base polymer from which they were prepared. However, further improvements in leveling properties would be desirable.
It is the object of this invention to provide a new class of hydrophobically modified cellulose ethers which give, among other applications, significantly better leveling properties in latex paint formulations than those obtained with the long chain alkyl substituted cellulose ethers of the two previously mentioned patents, without sacrificing the other good performance properties in latex paint applications. This has been achieved by the use of nonionic cellulose ethers having a sufficient degree of nonionic substitution selected from the class consisting of methyl, hydroxyethyl and hydroxypropyl which would cause them to be water soluble, and which are further substituted with alkylaryl hydrocarbon radicals having about 10 to 24 carbon atoms in an amount between about 0.2 weight percent and the amount which renders said cellulose ether less than 1 percent by weight soluble in water. The cellulose ether to be modified is preferably one of low to medium molecular weight, i.e. less than about 800,000 and preferably .Iadd.between .Iaddend.about 20,000 and 500,000 (about 75 to 1,800 D.P.) Examples of such alkylaryl modified cellulose ethers are hydroxyethylcelluloses modified with either nonylphenyl, dodecylphenyl, or dinonylphenyl alkylaryl groups containing alkylaryl substitution levels from 0.25 to 2.4 weight percent.
While any nonionic water soluble cellulose ether can be employed as a cellulose ether substrate used to form the products of this invention, the preferred cellulose ether substrate is hydroxyethylcellulose of about 50,000-400,000 molecular weight. The alkylaryl substituent can be attached to the cellulose ether substrate via an ether, ester or urethane linkage. Preferred is the ether linkage, as the reagents currently used to effect etherification are readily obtained, the reaction is similar to that commonly used for the initial etherification, and the reagents are more easily handled than the reagents employed for modification via the other linkages. The resulting linkage is also usually more resistant to further reactions.
Although the products of this invention are referred to as being "long chain alkylaryl group modified," it will be recognized that except in the case where modification is effected with an alkyl halide, the modifier is not a simple long chain alkylaryl group. The group is actually a hydroxyalkyl radical in the case of a glycidyl ether, a urethane radical in the case of an isocyanate, or an acyl radical in the case of an acid or acyl chloride. Nonetheless, the terminology "long chain alkylaryl group" is used and the number of carbon atoms referes only to those carbon atoms in the hydrocarbon portion of the modifying molecule. It does not include any carbon atoms in the connecting groups. Thus, hydroxyethylcellulose modified by reaction with nonylphenyl glycidyl ether is termed a C15 hydrophobic group (C6 +C9) modification of hydroxyethylcellulose. ##STR1##
Similar modifications using .[.ether.]. .Iadd.either .Iaddend.dodecylphenyl glycidyl ether or dinomylphenyl glycidyl ether would result in C18 and C24 hydrophobes, respectively.
Moreover, there may be additional spacer groups, of various lengths, between the standard connecting group mentioned above and the long chain alkylaryl group. Thus, products with the structure: ##STR2## have been prepared, where the hydrophobe group is still considered to be C15.
Methods of preparing mixed ethers of cellulose, i.e. products having more than one etherifying modifier attached to the same cellulose molecule are known to the art. The products of this invention can be prepared via essentially the same methods. The preferred procedure for preparing the mixed ethers of this invention comprises slurrying the nonionic cellulose ether in an inert organic diluent with alkali until swollen, and reacting with about a C10 to C24 alkylaryl glycidyl ether, with agitation and heat, until the reaction is complete. Residual alkali is then actualized, and the product is recovered, washed with inert diluents, and dried. The etherification can also be effected with a C10 to C24 halide, but these are sometimes less reactive, less efficient and more corrosive. Therefore, it is preferred to use the glycidyl ether.
Methods of preparation of alkyl hydrophobically modified cellulose ethers are described in U.S. Pat. No. 4,228,277. In addition, rather than isolating and reacting the dried cellulose ether with the alkylaryl glycidyl ether, it is also possible to conduct the reaction in situ, that is, immediately after the preparation of the base cellulose ether of the proper substitution level, without isolating the cellulose ether. In this variation, the alkylaryl glycidyl ether is added immediately upon completion of the preparation of the cellulose ether, e.g., hydroxyethylcellulose. The reaction mixture is then reacted at an appropriate temperature and time for the reaction to be completed. In both methods of preparation, it is necessary that conditions be provided to assure that the cellulose ether is swollen to the point that the modifier can react substantially uniformly on all cellulose ether molecular throughout.
The following examples illustrate the practice of this invention, which has industrial application in latex paint manufacture.
The nonylphenyl glycidyl ether used is a commercial product of Wilmington Chemical Company (Heloxy® WC-64; 90% pure).
Hydroxyethylcellulose was prepared by methods described in U.S. Pat. No. 4,084,060 in a 0.5 gallon CHEMCO stirred autoclave from 121.5 g cellulose; 1,600 ml t-butyl alcohol; 38.9 g sodium hydroxide in 152 ml of water; and 158 g ethylene oxide, at 80° C. Without cooling the reactor, nonylphenyl glycidyl ether (NPGE) dissolved in 20 ml t-butyl alcohol as added and the reactor heated to 110° C. The mixture was kept at 110° C. for 2 hours. The reactor was then cooled to below 40° C. and neutralized to a pH of 7-8. The product was purified by slurrying in 85% aqueous acetone, filtering, reslurrying in 100% acetone, filtering and drying in a laboratory fluid bed dryer. The products were cream colored solids.
Analytical data are given in Table 1.
TABLE 1__________________________________________________________________________ Grams of 1% nonylphenyl Weight % Brookfield %Example glycidyl nonylphenyl Hydroxy- Viscosity Ash asNo. ether added modifier ethyl M.S. (mPa · s) Na2 SO4__________________________________________________________________________Control A 0 0 4.1 44 6.5Control B 0 0 5.2 40 5.41 9 0.61 4 120 6.22 18 0.94 3.1 175 5.03 18 1.12 4 352 5.64 18 1.2 5.2 250 5.65 26 1.63 3.1 2120 5.36 26 2.42 5.2 2180 5.3__________________________________________________________________________
Table 1 illustrates the associative thickener characteristics of alkylaryl hydrophobically modified cellulose ethers to provide enhanced viscosity.
The dodecylphenyl glycidyl ether was prepared by a procedure described in U.S. Pat. No. 3,102,912. DDPGE was 80% pure and contained predominately the para isomer.
The dinonylphenyl glycidyl ether was prepared by a procedure described in Synthesis, February 1983, pp. 117-119. DNPGE was 99% pure and contained predominately the ortho-para isomer.
The poly(ethyleneoxy)nonpyphenyl glycidyl ether was prepared in the same manner as dinonylphenyl glycidyl ether except that poly(ethyleneoxy)9 nonyl-phenol (Igepal CO630 from GAF) was used instead of dinonylphenol. PEONPGE was 90% pure.
The dodecylphenyl glycidyl ether (DDPGE) or the dinonylphenyl glycidyl ether (DDPGE) was reacted with hydroxyethylcellulose prepared using the same amounts of ingredients described in examples 1 to 6, except for the amount of alkylaryl glycidyl ether. Poly(ethyleneoxy)9 nonylphenyl glycidyl ether (PEONPGE), 2.1 g, was reacted with 34.5 a HEC, prepared according to examples 1 to 6, in the presence of 250 ml tert-butyl alcohol (TBA), and 3.6 g sodium hydroxide in 27 g water, at 90° C. for 41/2 hours. Neutralization and product workup were similar to the procedures described for examples 1 to 6.
The amounts of the glycidyl ethers used and analyses of the products isolated are shown in Table 2.
TABLE 2______________________________________Ex- Grams of Weight % Hy- 1%am- phenyl Phenyl droxy Brookfieldple glycidyl glycidyl ether ethyl Viscosity % Ash asNo. ether added modifier M.S. (mPa · s) Na2 SO4______________________________________A. Dodecylphenyl glycidyl ether7 9.0 0.51 4.0 63 4.98 13.57 0.78 3.9 230 5.49 18.2 1.00 4.0 550 5.1B. Dimonylphenyl glycidyl ether10 12.0 0.25 4.1 56 4.011 18.2 0.46 4.1 135 4.912 25.0 0.62 4.1 300 3.6C. Poly(ethyleneoxy)9 nonylphenyl gylcidyl ether13 2.1 g/ ˜0.5 4.5 44 --34.5 g HEC______________________________________
The products of examples 1 to 13 were used in a semi-gloss white interior .Iadd.all .Iaddend.acrylic latex paint formulation (formulation 3; SG-41-3; Aqualon Company Natrosol® Plus booklet, p. 16), substituting these products for the Natrosol® Plus Thickener used in the formulation.
Details of the paint properties resulting are given in Table 3. All paints were thickened to a Stormer viscosity of about 90 K.U. Performance parameters are described in the Aqualon Company Natrosol® Plus booklet.
TABLE 3______________________________________Ex- Thick- Brushing Sagample ener Viscosity Level- Resistance 60°No. Sample (poises) Spatter ing (mils) Gloss______________________________________A. Nonylphenyl Modifier14 1 1.3 5 9 10 33.915 2 1.1 6 10 12 36.016 3 1.0 7 9 17 33.517 4 1.1 8 9 13 26.218 5 0.8 7 7 16 37.419 6 1.0 5 3 24 17.8B. Dodecylphenyl Modifier20 7 1.2 8 9 11 39.821 8 1.0 8 8 13 40.222 9 1.0 8 5 19 40.0C. Dinonylphenyl Modifier23 10 1.2 9 9 10 39.824 11 1.0 8 8 12 38.925 12 0.8 8 8 12 39.1D. Poly(ethyleneoxy)9 nonylphenyl Modifier26 13 1.2 6 9 10 --E Control (Natrosol ® Plus) (Long Chain Alkyl Modifier)27 11 9 5 20 31.0______________________________________
Several unusual effects have been observed to be caused by the products of this invention in latex paint formulations. Relative to a thickener comprises of a long chain alkyl hydrocarbon modifier such as the group in Natrosol® Plus, these alkylaryl modified HEC thickeners showed significantly better leveling properties in paint, with values of 8-10 (compared to a value of 5 for Natrosol® Plus). When the alkylaryl group was nonylphenyl, the paint leveling value increased as the amount of hydrophobic substitution increased, up to a nonylphenyl substitution value of about 1.5 weight percent. At higher amounts of substitution, paint leveling values decreased. Thus, optimum paint leveling was achieved with nonylphenyl substitution amounts of between 0.5 and 1.5 weight percent. Other paint properties such as spatter resistance, brushing viscosity, and gloss were comparable to those obtained with the long chain hydrocarbon alkyl modifier. Sag resistance properties were slightly poorer as the result of the better leveling properties; however, sag values were still within acceptable limits.
In addition, other alkylaryl modifiers, such as dodecylphenyl (C18) and dinonylphenyl (C24) also gave excellent leveling and sag resistance properties as did cellulose ethers with a long spacer group between the alkylaryl hydrophobic group and a standard connecting group, as in the cellulose ether with a poly(ethyleneoxy)9 nonylphenyl modifier.
Thickener sample Number 3 from Table 1 was used in a .Iadd.vinyl acrylic paint formulation--specifically, a .Iaddend.vinyl acetate/vinyl versatate latex paint formulation. A leveling rating of 6 was obtained, compared to a rating of 3 for Natrosol® Plus.
This example illustrates an improvement in leveling by use of an alkylaryl modified hydroxyethylcellulose, relative to Natrosol® Plus in a different type of latex paint.
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|U.S. Classification||536/90, 536/93, 106/172.1, 524/43, 524/44, 536/96, 536/94|
|International Classification||C09D201/00, C09D7/00, C09K3/00, C09D7/12, C09D131/02, C09D193/00, C07D303/22, C08B11/18, C08L1/28, C08B11/193|
|Cooperative Classification||C08B11/193, C08L1/28, C09D7/002, C09D131/02|
|European Classification||C09D7/00D, C09D131/02, C08B11/193|
|Nov 9, 1995||FPAY||Fee payment|
Year of fee payment: 4
|Nov 23, 1999||FPAY||Fee payment|
Year of fee payment: 8
|Jan 5, 2001||AS||Assignment|
|Dec 27, 2002||AS||Assignment|
|Dec 31, 2002||AS||Assignment|
|Dec 1, 2008||AS||Assignment|
Owner name: HERCULES INCORPORATED, DELAWARE
Free format text: PATENT TERMINATION CS-013616-0430;ASSIGNOR:CREDIT SUISSE, CAYMAN ISLANDS BRANCH;REEL/FRAME:021901/0297
Effective date: 20081113