CA1256332A - Absorption of additives into polymer surfaces from solution - Google Patents

Abstract

ABSORPTION OF ADDITIVES INTO POLYMER
SURFACES FROM SOLUTION

ABSTRACT OF THE DISCLOSURE
Polymeric articles or non-polymeric articles having polymeric coatings are treated to incorporate an additive in the surface by a process comprising contacting the surface with a solution of the additive in a mixture of two or more solvents of different solvating power and selectively absorbing the additive into the surface.

Description

3~

_ 1 _ ABSORPTION OF ADDITIVE:S
INTO POLYMER SURFACES
FROM SOLUTION

BACKGROUND OF THE INVENTION
Polymeric materials have enjoyed increas-ingly wider use in industrial and consumer products, replacing or supplementing other materials such as metals, wood and ceramics. Chemical additives are o.ten employed with the polymer to adapt the physical or chemical properties for particular needs. Thus, depending on requirements, it may be desirable to add one or more substances such as heat stabilizers, ultra-violet light stabili~ers, antistatic agents, colorants, electrically conductive materiais, flame retardant agents, smoke suppxessants, foaming agents, and othexs.
Incorporation of the additive may be accomplished by use of various methods, including dry, solution or melt blending with the polymer prior to or during thermal processing into the finished article. In some instanc-es, the additive is merely coated onto the surface of the polymeric article, as in the case of certain antistatic agents which dissipate static charges or light stabilizers which absorb ultraviolet radiation.
In one prior art procedure for incorporating an ultraviolet light stabilizer into the surface of a molded polyphenylene ether resin blend, the stabilizer is dissolved in a solvent, the molded piece is immersed in the solution, and the stabilizer is ab-sor~ed into the molded surface. A disadvantage of this procedure is that the solvent aggressively attacks the polymer surface, making it tacky when wet, and thus difficult to hanale until the surface is thoroughly dried.

_ 2 --INTRODUCTION TO THE INVENTION

The present invention comprises in one aspect, a novel method for incorporating an additive from solu-tion into a polymer surface, making use of a miscibleblend of at least two liquids, one of which is a relative-ly good solvent for the polymer and additive, the o~her of which is a poorer solvent or nonsolvent for the poly-mer. Upon contacting the polymer with the liquid blend, the additive is readily absorbed, yet the surface does not become tacky. A result is that the workpiece can be more easily handled immediately after treatment.
The method of this invention can be utilized to add various additives to pre-formed polymeric articles or to non-polymeric articles having a poly-meric coating or surfacing. Conditions can be reg-ulated to increase or decrease the amount of additive incorporated, as will be explained in greater detail.
Another facet of the inventio~ comprises articles which have been treated in accordance with the aforementioned method.

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DESCRIPTION OF THE INVENTION
In general, the process of the invention comprises the steps of (a) contacting an article comprising a polymeric surface with a solution of an additive for the polymer in a miscible blend of two or more liquids, at least one of which is a solvent for the polymer and at least one of which is a relatively poorer solvent, or nonsolvent, for the polymer;
~b) maintaining the contacting for a period sufficient to absorb an effecti~e amount of the addi-tive into the polymeric surface; and (c) drying the liquid blend from the sur-face to obtain an article having the additive incor-porated within.
By way of illustration, the additive oradditives with which the polymer surface is to be treated is (are) first dissolved in a blend of two or more liquids as described abo~e. The amount of addi-tives can be varied as described to prepare a dilute,medium strength or concentrated solution. Preferably, however, the additive is dissolved in amounts near or at the limit of solubility, so as to provide a longer lasting solution which has less need for replen-ishment as more of the additive is absorbed into thepolymer surface.
Examples of additives which may be employed are ultra~iolet light stabilizers, heat stabilizers, antioxidants, colorants (for example, pigments or dyes), antistatic agents, flame retardant agents, smoke su-ppressants, foaming agents, electrical conduc~ivity agents~ lubricants and abrasion resistants.
After the solution of the additive has been prepare~, the polymeric article is immersed in it. Any suitable container may be used for this purpose, in-~5~3~ 8CN 3583 _ 4 -cluding glass lined or stainless steel vessels.
Immersion t1mes vary from several seconds to several minutes or more, depending on a number of factors, including the nature of the polymer surface, the type of additive, the amount of additive to the incorporated and the composition of the solvent blend. Generally, the time period required for treatment can be shortened by use of a stronger solvent or solvents in the blend, or by the use of a higher ratio of better solvent to poorer solvent, either of which will facilitate absorp-tion of the additive into the surface. Conversely, longer treatment times are requi.ed with use of weaker solvents or a lower ratio of better solvent to poorer solvent in the blend.
Absorption of the additive may also be facilitated by heating the solvent blend shortly prior to or during contacting with the polymer surface.
Heating at elevated temperatures above room temperature e.g., above 23C, and up to the boiling point of the blend is possible, but care should be taken not to greatly exceed that temperature if an open container is used, otherwise undesira~le large amounts of the solvents may be lost to the atmosphere through volatil-ization.
After the immersion has been completed, the surface or surfaces of the article are dried to remove the solvent. Drying may be accomplished,for example, by permitting the article to stand at room temperature, or by blowing air across the wet surface/ or by heating in an enclosure, such as an oven.
The method which has been described is useful to incorporate additives into the surface of a broad spectrum of polymeric materials, including those of poly(al~enyl aromatics), for example, polystyrene;
polyvinyl chlorides; polyamides; polyesters, for example, 3~:

poly(alkylene terephthalates) such as polye-thylene terephthalate and polybutylene te~ephthalate; poly-urethanes (both polyester- and polyether-based);
polycarbonates; polyolefins; polyphenylene oxides (or ethers); polyacrylics; acrylonitrile-butadiene-styrene terpolymers (ABS); and so forth.
Special mention is made of polyphenylene oxide resin, and especially of homopolymers and copolymers made up of units of the formula 10 -'~~

Q" Q n in which Q, Q', Q" and Q"' are, independently, selected from among hydrogen, halogen, hydrocarbon, halo-hydrocarbon, hydrocarbonoxy, and halohydrocarbonoxy;
and n represents the total number of monomer units and is an integer of at least about 20, and more usually at least 50.
These can be prepared using known procedures, including those described in U~S. Patents 3,306,874 and 3,306,875, both issued February 28, 1967 20 to Hay, and U.S. Patents 3,257,357 and 3,2A7,358, both issued June 21, 1966 to Stamatoff, from the reaction of phenols including but not limited to:

2,6-dimethylphenol; 2,6-diethylphenol; 2,6-d.ibutyl-phenol; 2,6-dilaurylphenol; 2,6-dipropylphenol;
25 2,6-diphenyphenol, 2-methyl-6-ethylphenol; 2-methyl-6-cyclohexylphenol; 2-methyl-6-tolylphenol; 2-methyl-6-methoxyphenol; 2-methyl-6-butylphenol; 2,6-dimethoxy-phenol, 2,3,6-trimethylphenol; 2,3,5,6-tetramethylphenol;
and 2,6-diethoxyphenol.
Examples of some of the polymers which can thus be prepared are poly(2,6-dimethyl-1,4-phenylene .-ether), poly(2,6-diethyl-1,4-phenylene ether), poly - :, ~2~33~ 8CN 3583 (2,6-dibutyl-1,4-phenylene ether), poly(2,6-dilauryl-1, 4-phenylene ether), poly(2,6-dipropyl-1,4-phenylene ether), poly(2,6-diphenyl-1,4-phenylene ether~, poly (2-methyl-6~ethyl-1,4-phenylene ether~, poly(2-methyl-6-cyclohexyl-1,4~phenylene ether), poly(2-methyl-6-tolyl-1,4-phenylene ether), poly(2-methyl-6-methoxy-1, 4-phenylene ether), poly~2-methyl-6-butyl-1,4-phenylene ether), poly~2,6-dimethoxy-1,4-phenylene ether), poly (2,3,6~trimethyl-1,4-phenylene ether), poly(2,3,5,6-tetramethyl-1,4-phenylene ether), and poly(2,6-die-thoxy-1,4-phenylene ether). Also useful are copolymers prepared from mixtures of the aforementioned phenols, such as 2,6-dimethylphenol employed in conjunction with, for instance, 2,3,6=trimethylphenol or 2 methyl-6-butyl-phenol, to provide, for instance, poly(2,6-dimethyl-co-2,3,6-trimethyl-1,4-phenylene ether).
Most preferred are polymers within the above formula where Q and Q' are alkyl having from 1 t~ 4 carbon atoms, and especially poly(2,6-dimethyl-1,4-phenylene ether).
These resins can be used in combination withother polymeric materia~s such as rubber modified high impact polystyrene (HIPS) or impact modifying styrene co- and terpolymers, or still others, to form comp-ositions which are extrudable or moldable into variousshaped objects or coatings suitable for treatment in accordance with the process of this invention.
After treatment in accordance with this invention, the polymeric surface can be evaluated to determine the extent of additive absorption by use of any number of conventional testing procedures. With particular reference to ultraviolet light stabili~ers, for instance, this can take the form of exposing the treated surface to sunshine or artificial weathering devices, followed by measuring the degree of polymer ~ ~2$6332 8CN 3583 degradation by monitoring the change in tensile strength, carbonyl development, or, as shown in the working examples, yellowness index.
DESCRIPTION OF THE SPECIFIC EMBODI~ENTS
The process and articles in accordance with the invention are illustrated by the following examples.
~XAMPLE 1 A thermoplastic blend of 50 parts by weight of poly(2,6-dimethyl-1,4-phenylene ether) resin ~P ~, General Electric Company), 50 parts by weight, rubber modified high impact polystyrene (HIPS), 3 parts by weight of titanium dioxide, 0.15 part by weight of zinc oxide and 0.15 part by weight of æinc sulfide was prepared, extruded at 530F., and injection molded into 15 test piece~ at a barrel temperature of 500F. tl70F.
mold temperature).
The test pieces were then treated in accord-ance with the invention by immersion in a solution of 2-hydroxy-4~octyloxybenzophenone ~American Cyanamid's 20 Cyasorb W 531 light stabilizer) in 1:1 chloroform:
methanol, using the immersion times and stahilizer concentrations shown below. After treatment, the test pieces were directly exposed to fluorescent black light for up to 20 days time, with the color change (the initial pieces were white) being measured after 2, 8 and 20 days, respectively (shown below as yellow-ness index).
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~ 8CN 3583 _ 10_ Ea~AMPLE 2 This example also illustrates a method of treatment in accordance with the invention, but using Cyasorb 531~ light stabilizer in a different solvent blend than Example 1.
Injection molded test pieces in the shape of 4 inch diameter discs were prepared fxom a thermo-plastic blend of 45 parts ~y weight of poly(2,6-dimeth-yl-1,4-phenylene ether) resin (PPO), 55 parts by weight of rubber modified high impact polystyrene, 13 parts by weight of isopropylated triphenyl phosphate (FMC's - Kronitexr~0), 0.5 part by weight of tridecyl phosphite 1.5 parts by weight of polyethylene, 0.15 parts by weight of zinc oxide and 0.15 parts by weight of xinc sulfide.
The solvent ~lend was a 4:1 mixture of trichlorotrifluoroethane (Freonf~13):methylene chloride.
A portion was used to prepare a 5% by weight solution of Cyasorb 531. One test disc was not immersed at all.
A second disc was immersed in the solvent blend Ino addi~ive present) at room temperature (about 23C.).
A third was immersed in the blend at the boiling point of the solvent blend. A fourth was immersed in the 5%
solution at room temperature. The fifth was immersed in the 5~ solution at the boiling point. Immersion time was 5 seconds in every case.
The test discs were then exposed~r~ ultra-violet light radiation in a Hewlett-Packard HP W Tester.
The amount of irradiance was 60,000 mW/cm . The temp-erature was kept constant at 35C. The relative humid-ity was 50%. Test discs were rotated every other day to assure uniform exposure. The results were as follows:

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~ 8CN 3583 _ 11 _ TABL~ 2 - TIME TO CHANGE
IN YELLOWNESS INDEX OF 1.0 Test SamDle Time(hours) S 1. Control(no immersion) 40.0 2. Immersion Room Temp., No Additive 17O9 13 3. Immersion Boiling Point, No Additive 23.8 4. Immersion 5% Solution, greater than Room Temp. ~05 15 5.-Immersion 5% Solution, greater than Boiling Point 405 As shown, the exposure time re~uired for the test samples to exhibit a color change o ~YI = 1 was greatly increased by treatment with the 5% solution of Cyasorb 531 stabilizer in both cases.

This example illustrates the use of a solu-tion of 5% by weight of a 1:1 mixture of Cyasorb 531 and bis ~,2,6,6-tetramethyl-4-piperidinyl) sebacate (Tinuvin1~70) dissolved in a 4:1 blend of Freon 113 '~ and methylene chloride.
Test discs of the same composition and phy-sical dimensions as in the previous example were immersed in the solution for 5 seconds, in one case at room tem-perature, in another case at the boiling point. Expos-ure to ultraviolet light radiation was in a Hewlett-Packard HP W Tester, again using the same conditions as in Example 2. The yellowness index and change in yellow-ness index for each test sa~ple, at various time inter-vals, is reported below.

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_ 12 _ Sam~le 5 sec. R.T 5 sec. B.P.
YI~YI YI~YI
Exposure Time, hours 0.0 15.80 21.10 23.0 14.4-1.4 19.4-1.7 50.8 1~.4-1.4 19.3-1.~
137.7 14.4-1.4 19.3-1.8 208.5 ~4.6-1.2 19.5-1.6 10 300.7 14.8-1.0 19.6-1.4 375.2 14.9-0.9 19.6-1.4 405.4 15.0-0~8 19.8-1.3 The procedure of Example 3 was repeated, except using a solution comprised of 5~ by weight of Tinuvin 770 in a 4:1 blend of Freon 113 and methylene chloride. The exposure time required to show a yellowness index change of 1.0 was 39.7 hours in the case of the test ?0 sample immersed for 5 seconds at room temperature, and 42.5 hours for the test sample immersed for 5 seconds at the boiling point of the solution.
All of the absve mentioned patents and publications are incorporated herein by reference.
Other modifications and variations of the invention will occur to those skilled in the art in the light of the above disclosure. It is to be understood, therefore, that changes may be made in the specific embodiments which are within the scope of the invention defined in the appended claims.

Claims (14)

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:

1. A process for incorporating an additive into the polymeric surface of an article comprising a polyphenylene ether resin product, comprising the steps of:
(a) contacting said article having at least one said polymeric surface with a solution of an additive dissolved in a miscible blend of two or more liquids, at least one of which is a solvent for the polyphenylene ether resin product and additive, and at least one of which is a nonsolvent or poorer solvent;
(b) continuing the contact for a period of time sufficient for the polyphenylene ether resin product surface to absorb an effective amount of the additive; and (c) drying the liquid from the polymer surface to obtain an article having the additive incorporated in the surface, wherein the additive is selected from among light stabilizers, heat stabilizers, antioxidants, colorants, antistatic agents, flame retardant agents, smoke suppressants, foaming agents, electrical conductivity additives, lubri-cants, and abrasion resistants.

2. A process according to claim 1, in which in steps (a) and (b) the contacting is conducted at room temperature.

3. A process according to claim 1, in which in steps (a) and (b) the contacting is conducted at an elevated temperature above room temperature but below the boiling point of the additive solution.

4. A process according to claim 1, in which in steps (a) and (b) the contacting is conducted at or near the boiling point of the additive solution.

5. A process according to claim 1, in which contacting is effected by immersion.

6. A process according to claim 1, in which the additive is a light stabilizer.

7. A process according to claim 1, in which the polymer is a polyphenylene oxide resin.

8. A process according to claim 1, in which the polymer is a polyphenylene oxide homopolymer or copolymer having units of the formula in which Q, Q', Q" and Q''' are, independently, selected from among hydrogen, halogen, hydrocarbon, halohydrocarbon, hydrocarbonoxy, and halohydrocarbonoxy; and n represents the total number of monomer units and is an integer of at least about 20.

9. A process according to claim 8, in which the polyphenylene ether resin is poly(2,6-dimethyl-1,4-phenylene ether).

10. A process according to claim 8, in which the polyphenylene ether resin is in admixture with a styrene polymer.

11. A process according to claim 10, in which the styrene polymer is rubber modified high impact polystyrene.

12. A process according to claim 1, in which the miscible blend comprises chloroform and methanol.

13. A process according to claim 1, in which the miscible blend comprises trichlorotrifluoroethane and methylene chloride.

14. A process according to claim 1, in which the additive is 2-hydroxy-4-octyloxybenzophenone, or Tinuvin 770, or a mixture of both.