CA1332684C - Stain-resistant aromatic/maleic anhydride polymers - Google Patents
Stain-resistant aromatic/maleic anhydride polymersInfo
- Publication number
- CA1332684C CA1332684C CA000586056A CA586056A CA1332684C CA 1332684 C CA1332684 C CA 1332684C CA 000586056 A CA000586056 A CA 000586056A CA 586056 A CA586056 A CA 586056A CA 1332684 C CA1332684 C CA 1332684C
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- Prior art keywords
- polymer
- maleic anhydride
- stain
- unit derived
- mol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
- D06M15/277—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof containing fluorine
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/227—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of hydrocarbons, or reaction products thereof, e.g. afterhalogenated or sulfochlorinated
- D06M15/233—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of hydrocarbons, or reaction products thereof, e.g. afterhalogenated or sulfochlorinated aromatic, e.g. styrene
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/41—Phenol-aldehyde or phenol-ketone resins
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/16—Synthetic fibres, other than mineral fibres
- D06M2101/30—Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M2101/34—Polyamides
Abstract
TITLE
STAIN-RESISTANT AROMATIC/MALEIC ANHYDRIDE POLYMERS
ABSTRACT OF THE INVENTION
Stain-resistant, polyamide textile substrates treated with compositions comprising hydrolyzed ethylenically unsaturated aromatic/maleic anhydride polymers and processes for their preparation. The treated substrates possess stain resistance that is as good as or better than do previously known stain-resist treated substrates but do not suffer from yellowing to the extent that previously known treated substrates do.
STAIN-RESISTANT AROMATIC/MALEIC ANHYDRIDE POLYMERS
ABSTRACT OF THE INVENTION
Stain-resistant, polyamide textile substrates treated with compositions comprising hydrolyzed ethylenically unsaturated aromatic/maleic anhydride polymers and processes for their preparation. The treated substrates possess stain resistance that is as good as or better than do previously known stain-resist treated substrates but do not suffer from yellowing to the extent that previously known treated substrates do.
Description
13326~-1 TITLE
STAIN-RESISTANT AROMATIC/MALEIC ANHYDRIDE POLYMERS
FILED OF THE INVENTION
The present invention relates to polyamide textile substrates treated with stain-resistant compositions comprising hydrolyzed ethylenically unsaturated aromatic/maleic anhydride polymers, and processes for their preparation. The substrates of this invention possess stain resistance but do not suffer from yellowing to the extent that previously known materials do.
BACKGROUND OF THE INVENTION
Polyamide substrates, such as nylon carpeting, upholstery fabric and the like, are subject to staining by a variety of agents, e.g., foods and beverages. An especially troublesome staining agent is FD&C Red Dye No. 40, commonly found in soft drink preparations. Different types of treatments have been proposed to deal with staining problems. One approach is to apply a highly fluorinated polymer to the substrate. Another is to use a composition containing a sulfonated phenol-formaldehyde condensation product.
For example, Liss and Beck, in Canadian Patent No. 1,176,410, which issued on 1990 November 20 disclose stain-resistant synthetic polyamide textile substrates having modified sulfonated phenol-formaldehyde polymeric condensation products.
However, sulfonated phenol-formaldehyde condenation products are :
.. . . .
-: - ~ -. . -- -~ , 1 3~584 r 2 themselves sub~ect to discoloration; commonly they turn - yellow. Yellowing problems are descr~bed ~y W. H.
Hemmpel ~n a March 19, 1982 nrticle ~n ~merica's ~ex~ , entitled Reversible Yellow$na ~5~_Eirishe~'s Fault. ~emmpel attributes yellowin~ to ~xposure of a phenol-~ased finish to nitrogen ox~des ~nd/or ultra-- violet radiation. Critchley et ~1., He~t ~es~stant Polvmers, TechnoloaicallY_Useful Materials, ~lenum Pr~ss, N.Y. l9B3, state that the thermo-oxidat~ve ; 10 stability of phenol-formaldehyde condensation products ; can be improved by etherifying or esterifying the phenolic hydroxyl groups.
To deal wi~h the yellowing problem, M~rshall, .- ~ in U.S. Patent 4,833,009, ISSUed 1989 May 23, removes color-formers by dissolving the condensation product ~n aqueous base, ac~difying the solu~ion to form ~ slurry, heating the slurry so as to cause p~ase separation, recovering water-insoluble material and dissolving the water-insoluble mater~al ~n aqueous -~ 20 base. On the other band, ~iss and Beck, in their aforesaid application, remove color-for~ers by acylating or etherifying some of the phenolic hydroxyls of the condensat~on product, and in ~ preferred embodiment, dissolving the modi~ed condensation product in a hydroxy-cont~ining solvent, ~uch a5 ; ethylene glycol, pr~or to its being appl~ed to the text~le substrate.
Allen et al., in U.S. P~tent 3,835,071, disclose rug shampoo compos~tion~ which upon drying :; 30 leave very brittle, non-tacky res~dues which are easily removed when dry. The compositions comprise water-soluble metal, ammonium or amin~ salt of a styrene-maleic anhydride copolym~r, or its half ester, and a detergent. Water-soluble metal ~alts of Group II and tlle alkali metals (par'icularly magnesium and sodium) , ,,i ~' .
~,' ' .
b ~ . . , .
.:
_3_ 13~2~8~
are preferred and ammonium salts are most preferred by Allen et al.
BRIEF SUMMARY OF THE INVENTI~
The present invention provides polyamide textile substrates treated with hydrolyzed ethylenically unsaturated aromatic/maleic anhydride polymers so as to impart stain resistance to the substrates, and methods for preparing the same.
Commonly materials known in the past to be useful as stain blockers were sulfonated. Finding a non-sulfonated material, such as the hydrolyzed ethylenically unsaturated aromatic/maleic anhydride of this invention, to be useful for this purpose was unexpected.
DETAILED DESCRIPTION OF THE INVENTION
The hydrolyzed polymers suitable for the purposes of this invention contain between about one and two polymer units derived from one or more ethylenically unsaturated aromatic monomers per polymer unit derived from maleic anhydride (hydrolyzed polymers containing three ethylenically unsaturated aromatic polymer units per maleic anhydride polymer unit are not suitable). Hydrolyzed polymers containing about one polymer unit derived from one or more ethylenically unsaturated aromatic monomers per polymer unit derived from maleic anhydride are most effective in imparting stain resistance to textile substrates. A variety of ~;
ethylenically unsaturated aromatic compounds can be used for the purpose of preparing the hydrolized polymers of this invention. Those aromatic compounds can be represented by the formula -3- ;
~.. ., . ~, . . , - .
STAIN-RESISTANT AROMATIC/MALEIC ANHYDRIDE POLYMERS
FILED OF THE INVENTION
The present invention relates to polyamide textile substrates treated with stain-resistant compositions comprising hydrolyzed ethylenically unsaturated aromatic/maleic anhydride polymers, and processes for their preparation. The substrates of this invention possess stain resistance but do not suffer from yellowing to the extent that previously known materials do.
BACKGROUND OF THE INVENTION
Polyamide substrates, such as nylon carpeting, upholstery fabric and the like, are subject to staining by a variety of agents, e.g., foods and beverages. An especially troublesome staining agent is FD&C Red Dye No. 40, commonly found in soft drink preparations. Different types of treatments have been proposed to deal with staining problems. One approach is to apply a highly fluorinated polymer to the substrate. Another is to use a composition containing a sulfonated phenol-formaldehyde condensation product.
For example, Liss and Beck, in Canadian Patent No. 1,176,410, which issued on 1990 November 20 disclose stain-resistant synthetic polyamide textile substrates having modified sulfonated phenol-formaldehyde polymeric condensation products.
However, sulfonated phenol-formaldehyde condenation products are :
.. . . .
-: - ~ -. . -- -~ , 1 3~584 r 2 themselves sub~ect to discoloration; commonly they turn - yellow. Yellowing problems are descr~bed ~y W. H.
Hemmpel ~n a March 19, 1982 nrticle ~n ~merica's ~ex~ , entitled Reversible Yellow$na ~5~_Eirishe~'s Fault. ~emmpel attributes yellowin~ to ~xposure of a phenol-~ased finish to nitrogen ox~des ~nd/or ultra-- violet radiation. Critchley et ~1., He~t ~es~stant Polvmers, TechnoloaicallY_Useful Materials, ~lenum Pr~ss, N.Y. l9B3, state that the thermo-oxidat~ve ; 10 stability of phenol-formaldehyde condensation products ; can be improved by etherifying or esterifying the phenolic hydroxyl groups.
To deal wi~h the yellowing problem, M~rshall, .- ~ in U.S. Patent 4,833,009, ISSUed 1989 May 23, removes color-formers by dissolving the condensation product ~n aqueous base, ac~difying the solu~ion to form ~ slurry, heating the slurry so as to cause p~ase separation, recovering water-insoluble material and dissolving the water-insoluble mater~al ~n aqueous -~ 20 base. On the other band, ~iss and Beck, in their aforesaid application, remove color-for~ers by acylating or etherifying some of the phenolic hydroxyls of the condensat~on product, and in ~ preferred embodiment, dissolving the modi~ed condensation product in a hydroxy-cont~ining solvent, ~uch a5 ; ethylene glycol, pr~or to its being appl~ed to the text~le substrate.
Allen et al., in U.S. P~tent 3,835,071, disclose rug shampoo compos~tion~ which upon drying :; 30 leave very brittle, non-tacky res~dues which are easily removed when dry. The compositions comprise water-soluble metal, ammonium or amin~ salt of a styrene-maleic anhydride copolym~r, or its half ester, and a detergent. Water-soluble metal ~alts of Group II and tlle alkali metals (par'icularly magnesium and sodium) , ,,i ~' .
~,' ' .
b ~ . . , .
.:
_3_ 13~2~8~
are preferred and ammonium salts are most preferred by Allen et al.
BRIEF SUMMARY OF THE INVENTI~
The present invention provides polyamide textile substrates treated with hydrolyzed ethylenically unsaturated aromatic/maleic anhydride polymers so as to impart stain resistance to the substrates, and methods for preparing the same.
Commonly materials known in the past to be useful as stain blockers were sulfonated. Finding a non-sulfonated material, such as the hydrolyzed ethylenically unsaturated aromatic/maleic anhydride of this invention, to be useful for this purpose was unexpected.
DETAILED DESCRIPTION OF THE INVENTION
The hydrolyzed polymers suitable for the purposes of this invention contain between about one and two polymer units derived from one or more ethylenically unsaturated aromatic monomers per polymer unit derived from maleic anhydride (hydrolyzed polymers containing three ethylenically unsaturated aromatic polymer units per maleic anhydride polymer unit are not suitable). Hydrolyzed polymers containing about one polymer unit derived from one or more ethylenically unsaturated aromatic monomers per polymer unit derived from maleic anhydride are most effective in imparting stain resistance to textile substrates. A variety of ~;
ethylenically unsaturated aromatic compounds can be used for the purpose of preparing the hydrolized polymers of this invention. Those aromatic compounds can be represented by the formula -3- ;
~.. ., . ~, . . , - .
4- 13~268 4 ~' 5 . R4 - w~erein . ................................. R2 R is Rl-CH-C- or CH2-C~-CH2-;
- lQ Rl is H-, CH3-or - R2 is H- or CH3-;
~3 i~ ~-or CH30-:
`' 15 q R4 ~s H-, CH3-, or CH3~0-, and R3 plus R4 ~ -0-CH2-0-Specific examples of ethylenically unsaturated arsmatic . compounds suitable for the purposes o~ this invention ; 20 include styrene, ~lpha-~ethylstyrene, 4-~thyl styrene, ~ ~tilbene, 4-acetoxystilbene (used to prepare a hydrol~zed polymer from Daleic ~nhydride and 4-hydroxy-stilbene), eugenol, isoeugenol, 4-allylphenol, ~afrole, mixtures of the s~e, and the like. ~rom the stand-point of cost-e~fect$veness, a copolymer prepared from styrene ~nd maleic ~nhydride at a 1:1 molar ratio is -preferred. ~he hydrolyzed polymers can have ~olecular weights (number aver~ge) in the range between about 500 and 4000, preferably between about 800 and 2000. They are readily soluble, even ~t high concentrations, in .: water at neutral to alkal~ne pH: increasing dilution is needed at a p~ below 6. ~hey are also soluble in lower alcohols, such as methanol, and are somewhat soluble in acetic acid.
: 35 r~
~ . .
j ~, ,. . .
.
.
:~ .
b ~ ~
- lQ Rl is H-, CH3-or - R2 is H- or CH3-;
~3 i~ ~-or CH30-:
`' 15 q R4 ~s H-, CH3-, or CH3~0-, and R3 plus R4 ~ -0-CH2-0-Specific examples of ethylenically unsaturated arsmatic . compounds suitable for the purposes o~ this invention ; 20 include styrene, ~lpha-~ethylstyrene, 4-~thyl styrene, ~ ~tilbene, 4-acetoxystilbene (used to prepare a hydrol~zed polymer from Daleic ~nhydride and 4-hydroxy-stilbene), eugenol, isoeugenol, 4-allylphenol, ~afrole, mixtures of the s~e, and the like. ~rom the stand-point of cost-e~fect$veness, a copolymer prepared from styrene ~nd maleic ~nhydride at a 1:1 molar ratio is -preferred. ~he hydrolyzed polymers can have ~olecular weights (number aver~ge) in the range between about 500 and 4000, preferably between about 800 and 2000. They are readily soluble, even ~t high concentrations, in .: water at neutral to alkal~ne pH: increasing dilution is needed at a p~ below 6. ~hey are also soluble in lower alcohols, such as methanol, and are somewhat soluble in acetic acid.
: 35 r~
~ . .
j ~, ,. . .
.
.
:~ .
b ~ ~
The polymers suitable for the purposes of this invention can be prepared by hydrolyzing ethylenically unsaturated aromatic/maleic anhydride polymers. However, not just any hydrolyzin~ agent will give products of equivalent utility for the purposes of this invention. Alkali metal hydroxides are suitable hydrolyzing agents. While potassium and/or lithium hydroxides can be subtituted for sodium hydroxide in whole or in part as a hydrolyzing agent, the latter is preferred. Hydrolysis can be effected in the presence of more than or less than a molar amount of an alkali metal hydroxide, such as NaOH. But unless special measures are taken, hydrolysis of the polymer in the presence of ammonium hydroxide gives a product which does not provide satisfactory stainblocking properties to a polyamide textile substrate. Thus, if the polymer is hydrolyzed in the presence of ammonium hydroxide, it is essential that it be held at elevated temperature for an extended period of time thereafter; otherwise, the polymer imparts unsatisfactory stainblocking properties to polyamide substates. On the other hand, hydrolysis of the polymer in the presence of excess ammonium hydroxide results in a product which fails to ~;
impart satisfactory stainblocking properties to polyamide substrates even after having been held for an extended period of time at elevated temperature. -Neither should hydrolysis be carried out in the presence of an alcohol. Even in the presence of any of ~ ;
the bases described above, the ethylenically unsaturated aromatic/maleic anhydride polymer can react with the alcohol to form a half-ester which will be deleterious to the stain-resist performance of the hydrolyzed polymers.
The hydrolyzed ethylenically unsaturated aro~atic/maleic anhydride polymers of this invention ,,, .,.. - .;, . , ~ : .
,.
.:
, ,. , ~. .
1 3 ~
~dJl b~ used as such in treating polyamide textile substrates. They can be applied to dyed or undyed polyamide textile substrates. They can be applied to such substrates in the absence or presence of a polyfluoroorganic oil-, water-, and/or soil-repellent materials. In the alternative, such a polyfluoroorganic material can be applied to the textile substrate before or after application of the hydrolyzed polymers of this invention thereto. The hydrolyzed polymers can be applied to textile substrates in a variety of ways, e.g. during conventional beck and continuous dyeing procedures.
The quantities of the polymers of this invention which are applied to the textile substrate are amounts effective in imparting stain-resistance to the substrate. The amounts can be varied widely; in general, one can use between 0.1 and 2% by weight of them based on the weight of the textile substrate, usually 0.6% by weight or less. The polymers can be applied, as is common in the art, at pHs ranging between 4 and 5. However, more effective exhaust deposition can be obtained at a pH as low as 2. When pH of 2 is used, the preferred level of application to the textile substrate is about 0.6% by weight, based on the weight of the textile su~strate. More effective stainblocking is obtained if the hydrolyzed polymers are applied to the textile substrate at higher temperatures. For example, at pH 2, 170-F is preferred, and 200-F is preferred at pH 5. However, stainblocking can be obtained when application is effected at room temperature, or even at that of cold tap water (10-15C).
The hydrolyzed polymers of this invention can also be applied in-place to polyamide carpeting which J~ has already been .nstalled in a dwelling place, office : -:: -1332~
or other locale. They can be applied as a simple aqueous preparation or in the form of aqueous shampoo preparation, with or without one or more polyfluoro-organic oil-, water-, and/or soil-repellent ~aterials.
They may be applied at the levels described above, at temperatures described, and at a pH between about l and 12, preferably between about 2 and 9.
The following Examples are illustrative of the invention. Unless otherwise indicated, all parts and percentages are by weight and temperatures in the Examples and Tests are in degrees Celsius. In the examples that follow, stain resistance and yellowing were measured by the techniques described below.
Exhaust A~lication of Stain-Resists to Car~e~ina Launder-O-Meter Method Exhaust application of stain-resists to carpeting is carried out in a Launder-O-Meter automated dyeing machine. One carpet piece is contained in each of several (up to twenty) stainless steel, screw-cap canisters. The canisters are held in a rack that rotates in a water bath whose temperature is automatically controlled for rate of heating, time at temperature and cooling. For a typical application bath, one uses a 20 to 1 liguor to goods ratio with 2.5 weight % of the stain-resistant composition. The stain-resistant compositions can be applied at pH 2 or pH 5. At pH 2, an excess of sulfamic acid is used. At pH 5, an excess of ammonium sulfate is used, as well as 3g/L of magnesium sulfate and lg/L of an alkyl aryl sulfonate (AlkanolND) or a suitable leveling agent.
After the bath is made up, a solution of the stain-resist composition is added to the Launder-o-Meter canister. The carpet sample to be treated is then placed in t`~e canister, tufted side out, the size of .. .
.
!~, . . , ' .
1332~8~
the carpet sample, relative to the size of the canister, being such that the no portion of the sample touches another portion of the sample. The canisters are placed in the Launder-O-Meter and the water bath temperature is held at 110F for 5 minutes. The temperature of the water bath is then raised to the desired temperature for application of the stain-resist composition. For application at pH 2, the temperature of the water bath is raised to 170F + 5-F, and for application at pH 5, the temperature of th~ water bath is raised to 200F + 5-F. After the bath water reaches the des-ired temperature, it is held there for 20 min.
and then cooled to lOO-F. The treated carpet sample is removed from the canister and rinsed by squeezing in deionized water at room temperature. Three successive rinses in fresh deionized water are given, each rinse being at 40 volumes of water per volume of sample. The rinsed carpet sample is centrifuged to remove excess liquid and dried at 200-F. in a forced draft oven for 30 minutes. The dry carpet sample can then be tested by use of the tests described below.
Stain Tests ~. Stain Test A is used to measure the extent to which carpeting is stained by a commercial beverage composition which contains FD&C Red Dye No. 40 (an acid dye). The staining liquid, if sold commercially as a liquid, is used as is. Usually the commercial product is in the form of a solid. In that event, the beverage preparation, in dry, solid form, is dissolved in deionized water so as to provide 0.1 g of FD~C Red Dye l~o. 40 per liter of water. Sufficient wetting agent (Du Pont MerpolSE liquid nonionic ethylene oxide condensate) is added to the dye solution to provide 0.5 ~3 of the wetting age;~t per liter of dye solution.
',' ' .
''` . ' ` `
" . ' .
, . . .
.
1332~8~
Unless otherwise specified, the test sample is DuPont type 1150 Nylon 6,6 (white); Superba*
heatset, mock dyed level loop carpet, 3/8 inch pile height, 30 ounces per yard, 1/10 inch gauge, 10 stitches per inch, woven polypropylene primary backing. The test sample is wetted completely with water, and excess water is removed by centrifuging.
The damp sample is placed tufted face down in a pan and covered with ten times its face weight of stain fluid. Entrained air is expelled from the sample by squeezing or pressing. The sample is turned over and again the air is expelled. The sample is then returned to a face down position, and the pan is covered for storage for desired test period, namely 30 minutes or 24 hours. The stored stain sample is rinsed in running cool water until no more stain is visually detectable in the rinse water. The rinsed sample is extracted in a centrifuge and dried at 200 degrees F. Staining is evaluated with the Minolta*
Chroma Meter tristimulus color analyzer in the L*A*B
Difference Mode with the target sample set for the unstained carpet. The "a" value is a measure of redness, with a value of 43 equal to that obtained on an untreated carpet.
B. In Stain Test B, a 6 inch x 6 inch (15 cm x 15 cm) specimen of carpet is placed on a flat non-absorbent surface. 20 ml of the staining fluid described in Stain Test A is applied to the specimen of carpet by placing a 1~ inch x 2 inch ~3.8 cm x 5.1 cm) cylinder tightly over the specimen and pouring the staining liquid solution into the cylinder to contact the carpet specimen thereby forming a circular stain. the cylinder is then removed and excess staining solution is worked into the carpet tufts to achieve uniform staining. The stained carpet specimen is left undisturbed for 24 +
4 hours, after which it is rinsed * denotes trademarks C
: . ~
. ,' '.~ . ' , 133268~
thoroughly with cool water, squeezed dry, and excess solution removed. The stain resistance of the resulting carpet sample is visually determined by the amount of color left in the stained area of the carpet sample according to the following scale:
5 = no staining 4 = slight staining 3 = noticeable staining -2 = considerable staining 1 = heavy staining.
UV YELLOWING TEST
The light-fastness of carpet samples treated with a stainblocker is determined by exposing the lS treated samples to W light for 20 Hours. A sample piece of carpet that has been treated with a stain-blocker is placed in a box containing its hinged top a standard fluorescent fixture fitted with two forty watt lamps. Centered under the pair of lamps in the bottom of the box is a sliding tray having a 3 inch x 40 inch recess for holding carpet specimens. The depth of the recess is such that the distance from the carpet face to the plane defined by the lamp surfaces is 1 inch.
The current to the lamp is controlled by a timer so that a twenty-hour exposure can be obtained automatically. After the twenty-hour exposure, the reflectance of CIE White Light Source C from the carpet is compared with the reflectance from an unexposed sample and the CIELAB delta nb~ noted. Delta "b" is a measure of the yellow component of white light. A
Minolta Chroma Meter model CR-llO reflectance meter is used to make the measurements and to calculate delta "b" automatically from stored data on the unexposed sample. The value of nb~ is reported as the measure of .. .. .
~: .
. .
:
: ' ' .
- - . .
13~2~
yellowing with increasing positive values of "b"
corresponding to increased degrees of yellowing.
the Minolta Chroma Meter is used in the Hunter L*a*b color-deviation measuring mode tRichard Hunter, "Photoelectric Colorimetry with Three Filters," J. Opt. Soc. Am., 509-538 (1942)]. In the measuring mode, the inetrument measures the color differences between a "target" color, whose tristimulus color values have been entered into the microprocessor as a reference, and the sample color presented to the measuring head of the instrument.
In examining carpet samples for yellowing and for FD&C Red Dye No. 40 staining, the "target" color entered is that of the carpet before yellowing or staining. The color reflectance of the yellowed or stained carpet is then measured with the instrument and reported as:
*E, the total color difference, *L, the lightness value, *a, the redness value, if positive, or greenness, if negative, and *b, the yellowness value, if pGsitive, or blueness, if negative.
In a 7 gallon paste pail, 4800 gms of a 1/1 molar styrene/maleic anhydride copolymer having a number average molecular weight of 1600 (SMA*1000 from Sartomer) were stirred into 3000 gms of deionized water to give a smooth slurry. It dispersed well (no exotherm) in about 15 minutes.
Then over a~out 1 hour, 5400 gms of 30% NaOH were added. The reactor was cooled during addition to maintain temperature in the 30-40C range. If the temperature went over about 40C, addition of caustic solution was stopped. (Above 45C, the polymer may melt and coagulate into large * denotes trademark ; . - . , , ;
';, : `: : :, , -1332~8~
sticky globs which are very slow to hydrolyze.) After all of the NaOH solution has been added, the reaction mass was stirred for 15 minutes, then the reactor was heated to 70~c and stirred for 3 hours. Heating was stopped, and 2800 gms of deionized water was added with stirring, following by cooling to 50OC. A light yellow, slightly viscous, clear alkaline solution of a polysodium salt of styrene/maleic acid copolymer was obtained.
The solution thus obtained was applied to nylon carpet at 2-1/2 percent on weight of fiber in a simulated beck dyeing apparatus. The dried carpet was tested by saturating it with a solution of FD&C Red Dye No. 40 and letting it stand for 1/2 hsur a~ room temperature (Stain Test A described above). It was then rinsed with cold water. ~he treated carpet showed no evidence of staining while an untreated control was deeply stained red. In a similar test the carpet was allowed to stand for 24 hours in the acid dye solution;
on rinsing, the carpet treated with the above product solution of this Example 1 showed a noticeable pink stain while the untreated carpet was again stained a deep red. Carpets treated with the product solution of this Example 1 did not yellow on 24 hr. exposure to UV
light (Yellowing Test described above).
Control Example 1 was repeated using 2460 g. of ammonium hydroxide solution (28% NH3) instead of the 5400 g. of sodium hydroxide. A product similar in appearance to the product from Example 1 was obtained.
However, it provided little or no stain resistance in th~ 1/2 hr. Stain Test described above.
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-13- 133268~
To 40 g. of SMA 1000 dispersed in 30 ml. of water were added over the course of 1-1/4 hrs. 72 g. of 30% by weight potassium hydroxide with cooling to maintain the temperature at 30-40OC. After additio~
was completed, the solution was stirred for 1 hr.
without heating. The mass was allowed to stand overnight. In the morning, a trace of undissolved polymer was removed by filtration to yield the product which had stain resist and non-yellowing properties similar to the product of Example 1.
A solution of styrene (15.0 g., 0.14 mols), maleic anhydride (7.1 g., 0.14 mols), and dodecyl mercaptan (2.8 g., 0.014 mols), in toluene (101 g.) was heated to 70CC under nitrogen. Vazo~ 67 initiator [2,2'-azo-bis-(2-methylbutyronitrile)], 0.31 g., was added. A lO-C heat rise was noted,. After the exotherm subsided, the reaction mass was heated for 6 hrs. at 70 C. The polymer solution was then cooled to O-C in an ice water bath. The resulting white polymer precipitate was filtered and suction dried to constant weight, 19.2 g. This material was hydrolyzed according to the procedure of Example 1. A light yellow somewhat opaque solution was obtained.
Example 3 was repeated using stilbene (20.0 g., 0.21 mols) and maleic anhydride (10.9 g., 0.21 mols), and dodecyl mercaptan (2.3 g., 0.011 mols).
There obtained 29.2 g. of white polymer which on hydrolysis provided a white opaque dispersion with limited water solubility.
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~XAMPLE 5 A solution of styrene (7.5 g., 0.072 mol), trans-stilbene (13.0g., 0.072 mol), maleic anhydride (14.1 g., 0.144 mol) and dodecyl mercaptan (2.6 g., 0.013 mol) in deoxygenated methylisobutyl ketone (150 g) was heated to 60-C under nitrogen. To initiate polymerization, 2,2'-azo-bis-(2-methylbutyronitrile) (0.3 gram Vazo~ 67 brand) was added, resulting in a 5~c exotherm. After the exotherm subsided, the reaction mixture was heated for 8 hours at 70-C under nitrogen.
Methylisobutyl ketone was then removed by distillation under reduced pressure, yielding a slightly off-white solid mass (36.8 g) which was hydrolyzed according to the procedure of Example 1, giving a clear light yellow solution.
Example 6 A cut pile, beige saxony carpet produced from 15 dpf Suessen set nylon 66 staple yarn, stain-resist treated (the composition of Example 9 of said Liss and Beck U.S. patent application) and latexed and finished with a secondary polypropylene backing at a carpet mill, was tested per Stain Test B, and was found to exhibit slight staining (i.e. a stain rating of 4).
The carpet was cleaned in three passes with a 1:150 diluted shampoo (described below) using a Stanley Steemer truck mount. The carpet was treated in this manner "in placen at room temperature and was allowed to dry at room temperature. The dried treated carpet showed a very faint stain (a satisfactory stain rating of 4-5) when tested by Stain Test 2 (24 hours).
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ShamPoo Formulation Inqredient g6 Water 48 Na C12 SO4 18 Fluorosurfactant 4 Total 100 Definitions SMAC: 30 parts styrene/maleic anhydride copolymer (ARCO SMA 1000 resin), 36.2 parts water, 33.8 parts 30% NaOH combined and heated ~o hydrolyze the resin, using the procedure described in Example 1.
Na C12 SO4: 30% aqueous sodium lauryl sulfate.
PGME: Propylene glycol monomethyl ether DPM: Dipropylene glycol monomethyl ether Fluorosurfactant: A mixture of Li fluoroalkyl mercapto propionate and diethanolammonium fluoroalkyl phosphate in a 1.0:1.1 ratio.
Methyl isobutyl ketone (951.3 g) in a 4-neck 2.0 L flask fitted with mechanical agitation, condenser, temperature controller, nitrogen bubbler and heating mantle was heated to 70-C and sparged with nitrogen for one hour then cooled to room temperature.
To this solution were added maleic anhydride (98.06 g, 1.0 mol), stilbene (45.06 g, 0.25 mol), styrene (78.11 g., 0.75 mol), and dodecylmercaptan (16.6 g., 0.082 .,_. . . .
~- ; . .
. . .
1332~8~
mol). This mixture was heated to a steady 70C with stirring under a nitrogen sweep. VAZ0~ 67 initiator [2,2'-azobis--(2-methylbutyronitrile)] (2.21 g, 0.0115 mol) was then added in one portion as a solid, no appreciable exotherm was noticed. The reaction was stirred at 70 C for 3 hours then additional VAZ0~ 67 (1.1 G, 0.0057 mol) was added. The reaction continued to stir at 70-C for another 3 hours, then it was cooled to room temperature. Approximately 3/4 of the MIBK was then removed by rotary evaporation (or vacuum distillation at 10 mmHg). To the residual solution was added petroleum ether (ca. 1 L) to induce solidification of the polymer. The solid was collected by vacuum filtration and dried in a vacuum oven at 60-C
to give the terpolymer as a light yellow powder (233.9 g., 97% yield, MW = 1090 (VP0)).
To 560 g of water in a 4-neck 2.0 L flask fitted with mechanical agitation, temperature controller, condenser and heating mantle was added with stirring the terpolymer (200.0 g, ca. 0.84 mol). To this partially dispersed solution was added slowly at 30% sodium hydroxide solution (240 g, amount based on two mols of sodium hydroxide per mol of anhydride residue). The solution was heated to 80-C and stirred for 6 hours. The reaction was cooled to room temperature and any large residual particles were removed by vacuum filtration through a large buchner funnel ~6.8 g of solid was collected). A light yellow, slightly viscous, slightly cloudy alkaline solution of 30 the polysodium salt of stilbene-styrene-maleic acid ,~
terpolymer was obtain (996 g, 99.5% yield, 19.4% solids (active ingredient).
The product solution thus obtained was applied to nylon carpet at 5 percent (1 percent active ingre~ient) an weight of fiber i:- a simulated beck r, :
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133268~
dyeing apparatus at a pH of 2Ø The dried carpet was tested by saturating it with a solution of FD&C Red Dye No. 40 and letting it stand for 24 hours at room temperature. It was then rinsed with cold water. The treated carpet showed no evidence of staining while an untreated control was deeply stained red. Carpets treated with the terpolymer alone did not yellow on 24 hour exposure to W light.
In the simulated beck dying operation, a bath of the stain resist solution is made up in a glass screw cap container. A typical application bath utilizes a 20 to 1 liquor to goods ratio with 1.0 weight % of stain resist active ingredient on weight of fiber. An alkyl aryl sulfonate (Alkanol~ ND) or suitable leveling agent is also added at 15 % leveling agent on weight of stain resist active ingredient. The carpet piece ~DuPont type 1150 Nylon 6,6 white; Superba heat set, mock dyed level loop carpet, 3~8 inch pile height, 30 ounces per yard, 1/10 inch gauge, 10 stitches per inch, woven polypropylene primary backing) is then fully immersed with the tuft side facing the center and no overlap. The required pH adjustment is then made. A pH of 2.0 is standard unless otherwise noted. All pH adjustments were accomplished utilizing an aqueous 30 % sulfamic acid solution. The jar is then capped and placed in a 70-C constant temperature water bath. The jar is removed after 40 minutes and the sample allowed to cool to room temperature. The carpet sample is removed, rinsed under running deionized water and squeezed dry by hand. The carpet thus prepared is then fully immersed in a screw cap jar containing 0.1 g of FD & C red dye # 40 per 1 liter of water. The jar is capped and the carpet allowed to stand in the solution for 2~ hours. The carpet is removed and rinsed with tap ~ater until no more ~tain - . -! :
13~268~
is visually detectable in the rinse. The carpet is then dried in a 60xC oven and evaluated as described above.
A terpolymer was prepared in accordance with the procedure of Example 7, utilizing the following amounts of reactants and solvents:
MBIK (104.4 g) Styrene (4.1 g, 0.04 mol) Stilbene (10.8 g, 0.06 mol) Maleic Anhydride (9.8 g, 0110 mol) Dodecylmercaptan (1.4 g, 0.007 mol) Vazo 67 (0.26 g, 0.0013 mol).
Yield: 16.9 g The terpolymer was hydrolyzed in accordance with the procedure of Example 7, utilizing the following amounts of reactants and solvents:
Terpolymer (10.0 g) Deionized water (29.1 g) Aqueous NaO~I, conc. 30% (10.9 g).
A terpolymer was prepared in accordance with ~ t the procedure of Example 7, utilizing the following amounts of reactants and solvents:
MIBK (101.6 g) Styrene (5.2 g, 0.05 mol) Stilbene (9.0 g, 0.05 mol) Maleic Anhydride (9.8 g, 0.10 mol) Dodecylmercaptan (1.4 g, 0.007 mol) VAZO~ 67 (0.25 g, 0.0013 mol).
Yield: 19.1 g ~' ' ,,, ;
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1332~8~
The terpolymer was hydrolyzed in accordance with the procedure of Example 7, utilizing the following amounts of reactants and solvents:
Terpolymer (10.0 g) Deionized water (28.9 g) Aqueous NaOH, conc. 30% (11.1 g).
A terpolymer was prepared in accordance with the procedure of Example 8, utilizing the following amounts of reactants and solvents:
MIBK (98.4 g) Styrene (6.2 g, 0.06 mol) Stilbene (7.2 g, 0.04 mol) Maleic Anhydride (9.8 g, 0.10 mol) Dodecylmercaptan (1.4 g, 0.07 mol) VAZO 67 (0.24 g, 0.0012 mol) Yield: 19.1 g The terpolymer was hydrolyzed in accordance with the procedure of Example 7, utilizing the following amounts of reactants and solvents:
Terpolymer (10.0 g) Deionized water (28.5 g) Aqueous NaOH, conc. 30% (11.5 g).
A terpolymer was prepared in accordance with the procedure of Example 7, utilizing the following amounts of reactants and solvents:
MIBK (92.4 g) Styrene (8.3 g, 0.08 mol~
Stilbene (3.6 g, 0.02 moi) Maleic Anhydride (9.8 g, 0.10 mol) Dodecylmercaptan (1.4 g, 0.007 mol) VAZO~ 67 (0.23 g, 0.0012 mol) --19-- .
,' `
:.
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1332~84 Yield: 20.3 g The terpolymer was hydrolyzed in accordance with the procedure of Example 7, utilizng the following amounts of reactants and solvents:
Terpolymer (10.0 g) Deionized water (2B.2 g) Aqueous NaOH, conc. 30% (11.8 g).
A terpolymer was prepared in accordance with the procedure of Example 7, utilizing the following amount~ of reactants and solvents:
MIBK (92.4 g) Styrene (8.3 g, 0.08 mol) 15 Stilbene (3.6 g, 0.02 mol) Maleic Anhdyride (9.8 g, 0.10 mol) Dodecylmercaptan (1.4 g, 0.007 mol) VAZO~ 67 (0.23 g, 0.0012 mol) Yield: 20.3 The terpol,vmer was hydrolyzed in accordance with the procedure of Example 7, utilizing the following amounts of reactants and solvents:
Terpolymer (10.0 g) Deionized water (27.7 g) 25 Aqueous NaOH, conc. 30% (12.3 g).
A terpolymer was prepared in accordance with the procedure of Example 7, utilizing the following amounts of reactants and solvents:
MIBK (89.6 g) Styrene (9.4 g, 0.09 mol) Stilbene (1.8 g, 0.01 mol) Maleic Anhydride (9.B g, 0.10 mol) Dodecylmercaptan (1.4 g, 0.007 m~l) . , ~ .
1332~84 VAZOX 67 (0.21 g, 0.0011 mol) Yield: 19.6.g The terpolymer was hydrolyzed in accordance with the procedure of Example 7, utilizing the following amounts of reactants and solvents:
Terpolymer (10.0 g) Deionized water (27.3 g) Aqueous NaOH, conc. 30% (12.7 g3.
1o EXAMPLE 14 To a 4-neck 1 L flask fitted with nechanical agitation, condenser, addition funnel, nitrogen bubbler, and temperature controller was added, in order, THF (450 g), triethylamine (12.2 g, 0.12 mol), and 4-hydroxy stilbene (19.6 g, 0.10 mol). To this solution at room temperature was slowed added with stirring, via addition funnel, acetic anhdyride (12.3 g, 0.12 mol). When the addition of acetic anhydride was complete, the reaction solution was heated to 60-C
and held at this temperature with stirring for 2 hours.
The reaction was cooled to room temperature then THF
was removed in vacuo. The resulting residue was diluted with methylene chloride (500 mL) then extracted with 0.1 N HCl (1 X 500 mL), 30% saturated NaHCO3 (1 X
500 mL) and saturated NaCl (1 X 500 mL). The organic layer was dried over anhydrous sodium sulfate then filtered and concentrated in vacuo to give the 4-acetoxy stilbene as a light tan needle-like crystalline powder (22.7 g, 95~).
Methyl isobutyl ketone (1025 g) in a ~-neck 5.0 L flask fitted with mechanical agitation, condenser, temperature controller, nitrogen bubbler and heatin(~ mantle was heated to 70C and sparged with i -21-.,~ ~ , . , . . . . .
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133268~
nitrogen for one hour then cooled to room temperature.
To this solution were added maleic anhydride (98.06 g, 1.0 mol), 4-acetoxy stilbene (S9.6 g, 0.25 mol), styrene (78.11 g, 0.75 mol), and dodecylmercaptan (17.6 5 g, 0.0~7 mol). This mixture was heated to a steady 70~C with stirring under a nitrogen sweep. VAZO~ 67 initiator (2,2'-azobis-(2-methylbutyronitrile)] (2.3 g, 0.012 mol) was then added in one portion as a solid, no appreciable exotherm was noticed. The reaction was stirred at 70~C for 3 hours then additional VAZO0 67 (1.3 g, 0.067 mol) was added. The reaction was continued with stirring at 70C for another 5 hours;
then it was cooled to room temperature. Approximately 3/4 of the MIBK was then removed by rotary evaporation t 15 (or vacuum distillation at 10 mmHg). To the residual solution was added petroleum ether (ca. 1 L) to induce solidification of the polymer. The solid was collected by vacuum filtration and dried in a vacuum oven at 60 D C
to give the terpolymer as a light yellow powder 256 g, 100%).
To 689 g of water in a 4-neck 2.0 L flask fitted with mechanical agitation, temperature controller, condenser and heating mantle was added with stirring the terpolymer (256 g, ca. 1.0 mol). To this partially dispersed solution was added slowly a 30%
sodium hydroxide solution (333 g, amount based on two mols of sodium hydroxide per mol of anhydride residue plus the amount needed to hydrolyze the acetate group on the phenolic hydroxyl). The solution was heated to 80C and stirred for 6 hours. The reaction was cooled to room temperature and any large residual particles were removed by vacuum filtration through a large buchner funnel. A light brown, slightly viscous, slightly cloudy alkaline solution of the polysodium salt of 4-hydroxy stilbene/styrene/maleic acid 1332~8~
terpolymer was obtained (1264 g, 98.9% yield, 20 solids (active ingredient~).
The product solution thus obtained was applied to nylon carpet at 5 percent on weight of fiber (1 percent active ingredient) in a simulated beck dyeing apparatus as described in ~XAMPLE 7 at pH 2.0, 2.5, and 3Ø At pH 2.0 there was no evidence of staining, pH 2.5 showed a barely discernable pink stain, pH 3.0 was noticeably stained, while the untreated carpet was deeply stained red. Carpets treated with the terpolymer alone did not yellow on 24 hour exposure to W light.
A terpolymer was prepared in accordance with the procedure of Example 15, utilizing the following amounts of reactants and solvents:
MIBK (93.0 g) Styrene (9.37 g, 0.09 mol) 4-Acetoxy Stilbene (2.38 g, 0.01 mol) Maleic Anhydride (9.80 g, 0.10 mol) Dodecylmercaptan (1.61 g, 0.008 mol) VAZO 67 (0.23 g, 0.0012 mol) Yield: 19.7.
The terpolymer was hydrolyzed in aecordance with the procedure of Example 15, utilizing the following amounts of reactants and solvents:
Terpolymer (10.0 g) Deionized water (28.7 g) Aqueous NaOH, conc. 30% (12.2 g) Yield: 48.7 g.
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A terpolymer was prepared in accordance with the procedur~ of Example 15, utilizing the following amounts of reactants and solvents:
MIBK (146.0 g) Styrene (5.20 g, 0.05 mol) 4-Acetoxy Stilbene (11.9 g, 0.05 mol) Maleic Anhydride (9.80 g, 0.10 mol) Dodecylmercaptan (2.01 g, 0.0015 mol) Yield: 24.6 g.
The terpolymer was hydrolyzed in accordance with the procedure of Example 15, utilizing the following amounts of reactants and solvents:
Terpolymer (10.0 g) Deionized water (26.2 g) Aqueous NaOH, conc. 30% (13.8 g) Yield: 47.7 g.
Cumene (300 mls) was refluxed under nitrogen for one hour, cooled to 70-C and 14.7 g of maleic anhydride was added, followed by 20.28 g of styrene and 0.44 g of VAZO 67. White solids formed after 15 minutes. One hour after addition of the reactants was completed, the reaction mixture was cooled to room temperature and filtered. The resulting copolymer was then washed with 6 X 100 ml of petroleum ether. Yield of copolymer was 28.35 g. A portion of the copolymer (27.85g) was then added to 40 g of 30~ sodium hydroxide solution and 53 g of water and heated at 70-C for 6 hours. Yield was 111.6 g of a water solution of the hydrolyzed copolymer.
-25- 133268~
EXAMPLE l9 Methylisobutylketone (MIBK - 100 mls) was heated to 70CC with a stream of nitrogen bubbling below the surface of the liquid for 2-1/2 hours. The nitrogen stream was then removed from below the surface. However, the system was kept under a nitrogen atmosphere. Maleic anhydride (9.8 g) was added along with 1.82 g of dodecylmercaptan, 14.5 g of styrene and 0.26 g of VAZO~ 67 in that order. After heating for 3 lo hours at 75 C, an additional 0.13 g of VAZ0~ 67 was added and the reaction maintained at this temperature for 3 more hours. Yield of copolymer was 27.0 g.
Cumene (300 mls) was refluxed for one hour.
The temperature was then lowered to 75C and 14.7 g of maleic anhydride along with 30.0 g of eugenol acetate were added. Subsequently, 0.89 g of di-tert-butyl-peroxide was added. The reaction was then heated to 20 130-C and kept there for 12 hours. The copolymer was then filtered and washed with petroleum ether yielding 35.5 g of purified copolymer.
Example 20 was repeated except eugenol acetate was replaced with isoeugenol acetate. Yield of copolymer was 38.7 g.
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impart satisfactory stainblocking properties to polyamide substrates even after having been held for an extended period of time at elevated temperature. -Neither should hydrolysis be carried out in the presence of an alcohol. Even in the presence of any of ~ ;
the bases described above, the ethylenically unsaturated aromatic/maleic anhydride polymer can react with the alcohol to form a half-ester which will be deleterious to the stain-resist performance of the hydrolyzed polymers.
The hydrolyzed ethylenically unsaturated aro~atic/maleic anhydride polymers of this invention ,,, .,.. - .;, . , ~ : .
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~dJl b~ used as such in treating polyamide textile substrates. They can be applied to dyed or undyed polyamide textile substrates. They can be applied to such substrates in the absence or presence of a polyfluoroorganic oil-, water-, and/or soil-repellent materials. In the alternative, such a polyfluoroorganic material can be applied to the textile substrate before or after application of the hydrolyzed polymers of this invention thereto. The hydrolyzed polymers can be applied to textile substrates in a variety of ways, e.g. during conventional beck and continuous dyeing procedures.
The quantities of the polymers of this invention which are applied to the textile substrate are amounts effective in imparting stain-resistance to the substrate. The amounts can be varied widely; in general, one can use between 0.1 and 2% by weight of them based on the weight of the textile substrate, usually 0.6% by weight or less. The polymers can be applied, as is common in the art, at pHs ranging between 4 and 5. However, more effective exhaust deposition can be obtained at a pH as low as 2. When pH of 2 is used, the preferred level of application to the textile substrate is about 0.6% by weight, based on the weight of the textile su~strate. More effective stainblocking is obtained if the hydrolyzed polymers are applied to the textile substrate at higher temperatures. For example, at pH 2, 170-F is preferred, and 200-F is preferred at pH 5. However, stainblocking can be obtained when application is effected at room temperature, or even at that of cold tap water (10-15C).
The hydrolyzed polymers of this invention can also be applied in-place to polyamide carpeting which J~ has already been .nstalled in a dwelling place, office : -:: -1332~
or other locale. They can be applied as a simple aqueous preparation or in the form of aqueous shampoo preparation, with or without one or more polyfluoro-organic oil-, water-, and/or soil-repellent ~aterials.
They may be applied at the levels described above, at temperatures described, and at a pH between about l and 12, preferably between about 2 and 9.
The following Examples are illustrative of the invention. Unless otherwise indicated, all parts and percentages are by weight and temperatures in the Examples and Tests are in degrees Celsius. In the examples that follow, stain resistance and yellowing were measured by the techniques described below.
Exhaust A~lication of Stain-Resists to Car~e~ina Launder-O-Meter Method Exhaust application of stain-resists to carpeting is carried out in a Launder-O-Meter automated dyeing machine. One carpet piece is contained in each of several (up to twenty) stainless steel, screw-cap canisters. The canisters are held in a rack that rotates in a water bath whose temperature is automatically controlled for rate of heating, time at temperature and cooling. For a typical application bath, one uses a 20 to 1 liguor to goods ratio with 2.5 weight % of the stain-resistant composition. The stain-resistant compositions can be applied at pH 2 or pH 5. At pH 2, an excess of sulfamic acid is used. At pH 5, an excess of ammonium sulfate is used, as well as 3g/L of magnesium sulfate and lg/L of an alkyl aryl sulfonate (AlkanolND) or a suitable leveling agent.
After the bath is made up, a solution of the stain-resist composition is added to the Launder-o-Meter canister. The carpet sample to be treated is then placed in t`~e canister, tufted side out, the size of .. .
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1332~8~
the carpet sample, relative to the size of the canister, being such that the no portion of the sample touches another portion of the sample. The canisters are placed in the Launder-O-Meter and the water bath temperature is held at 110F for 5 minutes. The temperature of the water bath is then raised to the desired temperature for application of the stain-resist composition. For application at pH 2, the temperature of the water bath is raised to 170F + 5-F, and for application at pH 5, the temperature of th~ water bath is raised to 200F + 5-F. After the bath water reaches the des-ired temperature, it is held there for 20 min.
and then cooled to lOO-F. The treated carpet sample is removed from the canister and rinsed by squeezing in deionized water at room temperature. Three successive rinses in fresh deionized water are given, each rinse being at 40 volumes of water per volume of sample. The rinsed carpet sample is centrifuged to remove excess liquid and dried at 200-F. in a forced draft oven for 30 minutes. The dry carpet sample can then be tested by use of the tests described below.
Stain Tests ~. Stain Test A is used to measure the extent to which carpeting is stained by a commercial beverage composition which contains FD&C Red Dye No. 40 (an acid dye). The staining liquid, if sold commercially as a liquid, is used as is. Usually the commercial product is in the form of a solid. In that event, the beverage preparation, in dry, solid form, is dissolved in deionized water so as to provide 0.1 g of FD~C Red Dye l~o. 40 per liter of water. Sufficient wetting agent (Du Pont MerpolSE liquid nonionic ethylene oxide condensate) is added to the dye solution to provide 0.5 ~3 of the wetting age;~t per liter of dye solution.
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1332~8~
Unless otherwise specified, the test sample is DuPont type 1150 Nylon 6,6 (white); Superba*
heatset, mock dyed level loop carpet, 3/8 inch pile height, 30 ounces per yard, 1/10 inch gauge, 10 stitches per inch, woven polypropylene primary backing. The test sample is wetted completely with water, and excess water is removed by centrifuging.
The damp sample is placed tufted face down in a pan and covered with ten times its face weight of stain fluid. Entrained air is expelled from the sample by squeezing or pressing. The sample is turned over and again the air is expelled. The sample is then returned to a face down position, and the pan is covered for storage for desired test period, namely 30 minutes or 24 hours. The stored stain sample is rinsed in running cool water until no more stain is visually detectable in the rinse water. The rinsed sample is extracted in a centrifuge and dried at 200 degrees F. Staining is evaluated with the Minolta*
Chroma Meter tristimulus color analyzer in the L*A*B
Difference Mode with the target sample set for the unstained carpet. The "a" value is a measure of redness, with a value of 43 equal to that obtained on an untreated carpet.
B. In Stain Test B, a 6 inch x 6 inch (15 cm x 15 cm) specimen of carpet is placed on a flat non-absorbent surface. 20 ml of the staining fluid described in Stain Test A is applied to the specimen of carpet by placing a 1~ inch x 2 inch ~3.8 cm x 5.1 cm) cylinder tightly over the specimen and pouring the staining liquid solution into the cylinder to contact the carpet specimen thereby forming a circular stain. the cylinder is then removed and excess staining solution is worked into the carpet tufts to achieve uniform staining. The stained carpet specimen is left undisturbed for 24 +
4 hours, after which it is rinsed * denotes trademarks C
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thoroughly with cool water, squeezed dry, and excess solution removed. The stain resistance of the resulting carpet sample is visually determined by the amount of color left in the stained area of the carpet sample according to the following scale:
5 = no staining 4 = slight staining 3 = noticeable staining -2 = considerable staining 1 = heavy staining.
UV YELLOWING TEST
The light-fastness of carpet samples treated with a stainblocker is determined by exposing the lS treated samples to W light for 20 Hours. A sample piece of carpet that has been treated with a stain-blocker is placed in a box containing its hinged top a standard fluorescent fixture fitted with two forty watt lamps. Centered under the pair of lamps in the bottom of the box is a sliding tray having a 3 inch x 40 inch recess for holding carpet specimens. The depth of the recess is such that the distance from the carpet face to the plane defined by the lamp surfaces is 1 inch.
The current to the lamp is controlled by a timer so that a twenty-hour exposure can be obtained automatically. After the twenty-hour exposure, the reflectance of CIE White Light Source C from the carpet is compared with the reflectance from an unexposed sample and the CIELAB delta nb~ noted. Delta "b" is a measure of the yellow component of white light. A
Minolta Chroma Meter model CR-llO reflectance meter is used to make the measurements and to calculate delta "b" automatically from stored data on the unexposed sample. The value of nb~ is reported as the measure of .. .. .
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yellowing with increasing positive values of "b"
corresponding to increased degrees of yellowing.
the Minolta Chroma Meter is used in the Hunter L*a*b color-deviation measuring mode tRichard Hunter, "Photoelectric Colorimetry with Three Filters," J. Opt. Soc. Am., 509-538 (1942)]. In the measuring mode, the inetrument measures the color differences between a "target" color, whose tristimulus color values have been entered into the microprocessor as a reference, and the sample color presented to the measuring head of the instrument.
In examining carpet samples for yellowing and for FD&C Red Dye No. 40 staining, the "target" color entered is that of the carpet before yellowing or staining. The color reflectance of the yellowed or stained carpet is then measured with the instrument and reported as:
*E, the total color difference, *L, the lightness value, *a, the redness value, if positive, or greenness, if negative, and *b, the yellowness value, if pGsitive, or blueness, if negative.
In a 7 gallon paste pail, 4800 gms of a 1/1 molar styrene/maleic anhydride copolymer having a number average molecular weight of 1600 (SMA*1000 from Sartomer) were stirred into 3000 gms of deionized water to give a smooth slurry. It dispersed well (no exotherm) in about 15 minutes.
Then over a~out 1 hour, 5400 gms of 30% NaOH were added. The reactor was cooled during addition to maintain temperature in the 30-40C range. If the temperature went over about 40C, addition of caustic solution was stopped. (Above 45C, the polymer may melt and coagulate into large * denotes trademark ; . - . , , ;
';, : `: : :, , -1332~8~
sticky globs which are very slow to hydrolyze.) After all of the NaOH solution has been added, the reaction mass was stirred for 15 minutes, then the reactor was heated to 70~c and stirred for 3 hours. Heating was stopped, and 2800 gms of deionized water was added with stirring, following by cooling to 50OC. A light yellow, slightly viscous, clear alkaline solution of a polysodium salt of styrene/maleic acid copolymer was obtained.
The solution thus obtained was applied to nylon carpet at 2-1/2 percent on weight of fiber in a simulated beck dyeing apparatus. The dried carpet was tested by saturating it with a solution of FD&C Red Dye No. 40 and letting it stand for 1/2 hsur a~ room temperature (Stain Test A described above). It was then rinsed with cold water. ~he treated carpet showed no evidence of staining while an untreated control was deeply stained red. In a similar test the carpet was allowed to stand for 24 hours in the acid dye solution;
on rinsing, the carpet treated with the above product solution of this Example 1 showed a noticeable pink stain while the untreated carpet was again stained a deep red. Carpets treated with the product solution of this Example 1 did not yellow on 24 hr. exposure to UV
light (Yellowing Test described above).
Control Example 1 was repeated using 2460 g. of ammonium hydroxide solution (28% NH3) instead of the 5400 g. of sodium hydroxide. A product similar in appearance to the product from Example 1 was obtained.
However, it provided little or no stain resistance in th~ 1/2 hr. Stain Test described above.
, . .
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. :
-13- 133268~
To 40 g. of SMA 1000 dispersed in 30 ml. of water were added over the course of 1-1/4 hrs. 72 g. of 30% by weight potassium hydroxide with cooling to maintain the temperature at 30-40OC. After additio~
was completed, the solution was stirred for 1 hr.
without heating. The mass was allowed to stand overnight. In the morning, a trace of undissolved polymer was removed by filtration to yield the product which had stain resist and non-yellowing properties similar to the product of Example 1.
A solution of styrene (15.0 g., 0.14 mols), maleic anhydride (7.1 g., 0.14 mols), and dodecyl mercaptan (2.8 g., 0.014 mols), in toluene (101 g.) was heated to 70CC under nitrogen. Vazo~ 67 initiator [2,2'-azo-bis-(2-methylbutyronitrile)], 0.31 g., was added. A lO-C heat rise was noted,. After the exotherm subsided, the reaction mass was heated for 6 hrs. at 70 C. The polymer solution was then cooled to O-C in an ice water bath. The resulting white polymer precipitate was filtered and suction dried to constant weight, 19.2 g. This material was hydrolyzed according to the procedure of Example 1. A light yellow somewhat opaque solution was obtained.
Example 3 was repeated using stilbene (20.0 g., 0.21 mols) and maleic anhydride (10.9 g., 0.21 mols), and dodecyl mercaptan (2.3 g., 0.011 mols).
There obtained 29.2 g. of white polymer which on hydrolysis provided a white opaque dispersion with limited water solubility.
. .
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' 133268~
~XAMPLE 5 A solution of styrene (7.5 g., 0.072 mol), trans-stilbene (13.0g., 0.072 mol), maleic anhydride (14.1 g., 0.144 mol) and dodecyl mercaptan (2.6 g., 0.013 mol) in deoxygenated methylisobutyl ketone (150 g) was heated to 60-C under nitrogen. To initiate polymerization, 2,2'-azo-bis-(2-methylbutyronitrile) (0.3 gram Vazo~ 67 brand) was added, resulting in a 5~c exotherm. After the exotherm subsided, the reaction mixture was heated for 8 hours at 70-C under nitrogen.
Methylisobutyl ketone was then removed by distillation under reduced pressure, yielding a slightly off-white solid mass (36.8 g) which was hydrolyzed according to the procedure of Example 1, giving a clear light yellow solution.
Example 6 A cut pile, beige saxony carpet produced from 15 dpf Suessen set nylon 66 staple yarn, stain-resist treated (the composition of Example 9 of said Liss and Beck U.S. patent application) and latexed and finished with a secondary polypropylene backing at a carpet mill, was tested per Stain Test B, and was found to exhibit slight staining (i.e. a stain rating of 4).
The carpet was cleaned in three passes with a 1:150 diluted shampoo (described below) using a Stanley Steemer truck mount. The carpet was treated in this manner "in placen at room temperature and was allowed to dry at room temperature. The dried treated carpet showed a very faint stain (a satisfactory stain rating of 4-5) when tested by Stain Test 2 (24 hours).
:, ' ' '~ ', :' .
. . - .. , . . . .
. . .
ShamPoo Formulation Inqredient g6 Water 48 Na C12 SO4 18 Fluorosurfactant 4 Total 100 Definitions SMAC: 30 parts styrene/maleic anhydride copolymer (ARCO SMA 1000 resin), 36.2 parts water, 33.8 parts 30% NaOH combined and heated ~o hydrolyze the resin, using the procedure described in Example 1.
Na C12 SO4: 30% aqueous sodium lauryl sulfate.
PGME: Propylene glycol monomethyl ether DPM: Dipropylene glycol monomethyl ether Fluorosurfactant: A mixture of Li fluoroalkyl mercapto propionate and diethanolammonium fluoroalkyl phosphate in a 1.0:1.1 ratio.
Methyl isobutyl ketone (951.3 g) in a 4-neck 2.0 L flask fitted with mechanical agitation, condenser, temperature controller, nitrogen bubbler and heating mantle was heated to 70-C and sparged with nitrogen for one hour then cooled to room temperature.
To this solution were added maleic anhydride (98.06 g, 1.0 mol), stilbene (45.06 g, 0.25 mol), styrene (78.11 g., 0.75 mol), and dodecylmercaptan (16.6 g., 0.082 .,_. . . .
~- ; . .
. . .
1332~8~
mol). This mixture was heated to a steady 70C with stirring under a nitrogen sweep. VAZ0~ 67 initiator [2,2'-azobis--(2-methylbutyronitrile)] (2.21 g, 0.0115 mol) was then added in one portion as a solid, no appreciable exotherm was noticed. The reaction was stirred at 70 C for 3 hours then additional VAZ0~ 67 (1.1 G, 0.0057 mol) was added. The reaction continued to stir at 70-C for another 3 hours, then it was cooled to room temperature. Approximately 3/4 of the MIBK was then removed by rotary evaporation (or vacuum distillation at 10 mmHg). To the residual solution was added petroleum ether (ca. 1 L) to induce solidification of the polymer. The solid was collected by vacuum filtration and dried in a vacuum oven at 60-C
to give the terpolymer as a light yellow powder (233.9 g., 97% yield, MW = 1090 (VP0)).
To 560 g of water in a 4-neck 2.0 L flask fitted with mechanical agitation, temperature controller, condenser and heating mantle was added with stirring the terpolymer (200.0 g, ca. 0.84 mol). To this partially dispersed solution was added slowly at 30% sodium hydroxide solution (240 g, amount based on two mols of sodium hydroxide per mol of anhydride residue). The solution was heated to 80-C and stirred for 6 hours. The reaction was cooled to room temperature and any large residual particles were removed by vacuum filtration through a large buchner funnel ~6.8 g of solid was collected). A light yellow, slightly viscous, slightly cloudy alkaline solution of 30 the polysodium salt of stilbene-styrene-maleic acid ,~
terpolymer was obtain (996 g, 99.5% yield, 19.4% solids (active ingredient).
The product solution thus obtained was applied to nylon carpet at 5 percent (1 percent active ingre~ient) an weight of fiber i:- a simulated beck r, :
,~.'i . : .
.
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133268~
dyeing apparatus at a pH of 2Ø The dried carpet was tested by saturating it with a solution of FD&C Red Dye No. 40 and letting it stand for 24 hours at room temperature. It was then rinsed with cold water. The treated carpet showed no evidence of staining while an untreated control was deeply stained red. Carpets treated with the terpolymer alone did not yellow on 24 hour exposure to W light.
In the simulated beck dying operation, a bath of the stain resist solution is made up in a glass screw cap container. A typical application bath utilizes a 20 to 1 liquor to goods ratio with 1.0 weight % of stain resist active ingredient on weight of fiber. An alkyl aryl sulfonate (Alkanol~ ND) or suitable leveling agent is also added at 15 % leveling agent on weight of stain resist active ingredient. The carpet piece ~DuPont type 1150 Nylon 6,6 white; Superba heat set, mock dyed level loop carpet, 3~8 inch pile height, 30 ounces per yard, 1/10 inch gauge, 10 stitches per inch, woven polypropylene primary backing) is then fully immersed with the tuft side facing the center and no overlap. The required pH adjustment is then made. A pH of 2.0 is standard unless otherwise noted. All pH adjustments were accomplished utilizing an aqueous 30 % sulfamic acid solution. The jar is then capped and placed in a 70-C constant temperature water bath. The jar is removed after 40 minutes and the sample allowed to cool to room temperature. The carpet sample is removed, rinsed under running deionized water and squeezed dry by hand. The carpet thus prepared is then fully immersed in a screw cap jar containing 0.1 g of FD & C red dye # 40 per 1 liter of water. The jar is capped and the carpet allowed to stand in the solution for 2~ hours. The carpet is removed and rinsed with tap ~ater until no more ~tain - . -! :
13~268~
is visually detectable in the rinse. The carpet is then dried in a 60xC oven and evaluated as described above.
A terpolymer was prepared in accordance with the procedure of Example 7, utilizing the following amounts of reactants and solvents:
MBIK (104.4 g) Styrene (4.1 g, 0.04 mol) Stilbene (10.8 g, 0.06 mol) Maleic Anhydride (9.8 g, 0110 mol) Dodecylmercaptan (1.4 g, 0.007 mol) Vazo 67 (0.26 g, 0.0013 mol).
Yield: 16.9 g The terpolymer was hydrolyzed in accordance with the procedure of Example 7, utilizing the following amounts of reactants and solvents:
Terpolymer (10.0 g) Deionized water (29.1 g) Aqueous NaO~I, conc. 30% (10.9 g).
A terpolymer was prepared in accordance with ~ t the procedure of Example 7, utilizing the following amounts of reactants and solvents:
MIBK (101.6 g) Styrene (5.2 g, 0.05 mol) Stilbene (9.0 g, 0.05 mol) Maleic Anhydride (9.8 g, 0.10 mol) Dodecylmercaptan (1.4 g, 0.007 mol) VAZO~ 67 (0.25 g, 0.0013 mol).
Yield: 19.1 g ~' ' ,,, ;
.-~ ' ' . , .
.. :
,, ~
1332~8~
The terpolymer was hydrolyzed in accordance with the procedure of Example 7, utilizing the following amounts of reactants and solvents:
Terpolymer (10.0 g) Deionized water (28.9 g) Aqueous NaOH, conc. 30% (11.1 g).
A terpolymer was prepared in accordance with the procedure of Example 8, utilizing the following amounts of reactants and solvents:
MIBK (98.4 g) Styrene (6.2 g, 0.06 mol) Stilbene (7.2 g, 0.04 mol) Maleic Anhydride (9.8 g, 0.10 mol) Dodecylmercaptan (1.4 g, 0.07 mol) VAZO 67 (0.24 g, 0.0012 mol) Yield: 19.1 g The terpolymer was hydrolyzed in accordance with the procedure of Example 7, utilizing the following amounts of reactants and solvents:
Terpolymer (10.0 g) Deionized water (28.5 g) Aqueous NaOH, conc. 30% (11.5 g).
A terpolymer was prepared in accordance with the procedure of Example 7, utilizing the following amounts of reactants and solvents:
MIBK (92.4 g) Styrene (8.3 g, 0.08 mol~
Stilbene (3.6 g, 0.02 moi) Maleic Anhydride (9.8 g, 0.10 mol) Dodecylmercaptan (1.4 g, 0.007 mol) VAZO~ 67 (0.23 g, 0.0012 mol) --19-- .
,' `
:.
~- ' : ' . ,; :
. ~ .. .. .
. .
1332~84 Yield: 20.3 g The terpolymer was hydrolyzed in accordance with the procedure of Example 7, utilizng the following amounts of reactants and solvents:
Terpolymer (10.0 g) Deionized water (2B.2 g) Aqueous NaOH, conc. 30% (11.8 g).
A terpolymer was prepared in accordance with the procedure of Example 7, utilizing the following amount~ of reactants and solvents:
MIBK (92.4 g) Styrene (8.3 g, 0.08 mol) 15 Stilbene (3.6 g, 0.02 mol) Maleic Anhdyride (9.8 g, 0.10 mol) Dodecylmercaptan (1.4 g, 0.007 mol) VAZO~ 67 (0.23 g, 0.0012 mol) Yield: 20.3 The terpol,vmer was hydrolyzed in accordance with the procedure of Example 7, utilizing the following amounts of reactants and solvents:
Terpolymer (10.0 g) Deionized water (27.7 g) 25 Aqueous NaOH, conc. 30% (12.3 g).
A terpolymer was prepared in accordance with the procedure of Example 7, utilizing the following amounts of reactants and solvents:
MIBK (89.6 g) Styrene (9.4 g, 0.09 mol) Stilbene (1.8 g, 0.01 mol) Maleic Anhydride (9.B g, 0.10 mol) Dodecylmercaptan (1.4 g, 0.007 m~l) . , ~ .
1332~84 VAZOX 67 (0.21 g, 0.0011 mol) Yield: 19.6.g The terpolymer was hydrolyzed in accordance with the procedure of Example 7, utilizing the following amounts of reactants and solvents:
Terpolymer (10.0 g) Deionized water (27.3 g) Aqueous NaOH, conc. 30% (12.7 g3.
1o EXAMPLE 14 To a 4-neck 1 L flask fitted with nechanical agitation, condenser, addition funnel, nitrogen bubbler, and temperature controller was added, in order, THF (450 g), triethylamine (12.2 g, 0.12 mol), and 4-hydroxy stilbene (19.6 g, 0.10 mol). To this solution at room temperature was slowed added with stirring, via addition funnel, acetic anhdyride (12.3 g, 0.12 mol). When the addition of acetic anhydride was complete, the reaction solution was heated to 60-C
and held at this temperature with stirring for 2 hours.
The reaction was cooled to room temperature then THF
was removed in vacuo. The resulting residue was diluted with methylene chloride (500 mL) then extracted with 0.1 N HCl (1 X 500 mL), 30% saturated NaHCO3 (1 X
500 mL) and saturated NaCl (1 X 500 mL). The organic layer was dried over anhydrous sodium sulfate then filtered and concentrated in vacuo to give the 4-acetoxy stilbene as a light tan needle-like crystalline powder (22.7 g, 95~).
Methyl isobutyl ketone (1025 g) in a ~-neck 5.0 L flask fitted with mechanical agitation, condenser, temperature controller, nitrogen bubbler and heatin(~ mantle was heated to 70C and sparged with i -21-.,~ ~ , . , . . . . .
. . , ~ ., ~ .
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133268~
nitrogen for one hour then cooled to room temperature.
To this solution were added maleic anhydride (98.06 g, 1.0 mol), 4-acetoxy stilbene (S9.6 g, 0.25 mol), styrene (78.11 g, 0.75 mol), and dodecylmercaptan (17.6 5 g, 0.0~7 mol). This mixture was heated to a steady 70~C with stirring under a nitrogen sweep. VAZO~ 67 initiator (2,2'-azobis-(2-methylbutyronitrile)] (2.3 g, 0.012 mol) was then added in one portion as a solid, no appreciable exotherm was noticed. The reaction was stirred at 70~C for 3 hours then additional VAZO0 67 (1.3 g, 0.067 mol) was added. The reaction was continued with stirring at 70C for another 5 hours;
then it was cooled to room temperature. Approximately 3/4 of the MIBK was then removed by rotary evaporation t 15 (or vacuum distillation at 10 mmHg). To the residual solution was added petroleum ether (ca. 1 L) to induce solidification of the polymer. The solid was collected by vacuum filtration and dried in a vacuum oven at 60 D C
to give the terpolymer as a light yellow powder 256 g, 100%).
To 689 g of water in a 4-neck 2.0 L flask fitted with mechanical agitation, temperature controller, condenser and heating mantle was added with stirring the terpolymer (256 g, ca. 1.0 mol). To this partially dispersed solution was added slowly a 30%
sodium hydroxide solution (333 g, amount based on two mols of sodium hydroxide per mol of anhydride residue plus the amount needed to hydrolyze the acetate group on the phenolic hydroxyl). The solution was heated to 80C and stirred for 6 hours. The reaction was cooled to room temperature and any large residual particles were removed by vacuum filtration through a large buchner funnel. A light brown, slightly viscous, slightly cloudy alkaline solution of the polysodium salt of 4-hydroxy stilbene/styrene/maleic acid 1332~8~
terpolymer was obtained (1264 g, 98.9% yield, 20 solids (active ingredient~).
The product solution thus obtained was applied to nylon carpet at 5 percent on weight of fiber (1 percent active ingredient) in a simulated beck dyeing apparatus as described in ~XAMPLE 7 at pH 2.0, 2.5, and 3Ø At pH 2.0 there was no evidence of staining, pH 2.5 showed a barely discernable pink stain, pH 3.0 was noticeably stained, while the untreated carpet was deeply stained red. Carpets treated with the terpolymer alone did not yellow on 24 hour exposure to W light.
A terpolymer was prepared in accordance with the procedure of Example 15, utilizing the following amounts of reactants and solvents:
MIBK (93.0 g) Styrene (9.37 g, 0.09 mol) 4-Acetoxy Stilbene (2.38 g, 0.01 mol) Maleic Anhydride (9.80 g, 0.10 mol) Dodecylmercaptan (1.61 g, 0.008 mol) VAZO 67 (0.23 g, 0.0012 mol) Yield: 19.7.
The terpolymer was hydrolyzed in aecordance with the procedure of Example 15, utilizing the following amounts of reactants and solvents:
Terpolymer (10.0 g) Deionized water (28.7 g) Aqueous NaOH, conc. 30% (12.2 g) Yield: 48.7 g.
3~
,','' ' ' "''~'`' ~ ~
!:' ~ . `; ' ~ .
A terpolymer was prepared in accordance with the procedur~ of Example 15, utilizing the following amounts of reactants and solvents:
MIBK (146.0 g) Styrene (5.20 g, 0.05 mol) 4-Acetoxy Stilbene (11.9 g, 0.05 mol) Maleic Anhydride (9.80 g, 0.10 mol) Dodecylmercaptan (2.01 g, 0.0015 mol) Yield: 24.6 g.
The terpolymer was hydrolyzed in accordance with the procedure of Example 15, utilizing the following amounts of reactants and solvents:
Terpolymer (10.0 g) Deionized water (26.2 g) Aqueous NaOH, conc. 30% (13.8 g) Yield: 47.7 g.
Cumene (300 mls) was refluxed under nitrogen for one hour, cooled to 70-C and 14.7 g of maleic anhydride was added, followed by 20.28 g of styrene and 0.44 g of VAZO 67. White solids formed after 15 minutes. One hour after addition of the reactants was completed, the reaction mixture was cooled to room temperature and filtered. The resulting copolymer was then washed with 6 X 100 ml of petroleum ether. Yield of copolymer was 28.35 g. A portion of the copolymer (27.85g) was then added to 40 g of 30~ sodium hydroxide solution and 53 g of water and heated at 70-C for 6 hours. Yield was 111.6 g of a water solution of the hydrolyzed copolymer.
-25- 133268~
EXAMPLE l9 Methylisobutylketone (MIBK - 100 mls) was heated to 70CC with a stream of nitrogen bubbling below the surface of the liquid for 2-1/2 hours. The nitrogen stream was then removed from below the surface. However, the system was kept under a nitrogen atmosphere. Maleic anhydride (9.8 g) was added along with 1.82 g of dodecylmercaptan, 14.5 g of styrene and 0.26 g of VAZO~ 67 in that order. After heating for 3 lo hours at 75 C, an additional 0.13 g of VAZ0~ 67 was added and the reaction maintained at this temperature for 3 more hours. Yield of copolymer was 27.0 g.
Cumene (300 mls) was refluxed for one hour.
The temperature was then lowered to 75C and 14.7 g of maleic anhydride along with 30.0 g of eugenol acetate were added. Subsequently, 0.89 g of di-tert-butyl-peroxide was added. The reaction was then heated to 20 130-C and kept there for 12 hours. The copolymer was then filtered and washed with petroleum ether yielding 35.5 g of purified copolymer.
Example 20 was repeated except eugenol acetate was replaced with isoeugenol acetate. Yield of copolymer was 38.7 g.
'S. ~ .
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Claims (14)
1. A stain-resistant polyamide textile substrate having deposited on it an effective amount of a composition which imparts slain resistance to it comprising a polymer containing between about one and two polymer units derived from one or more ethylenically unsaturated aromatic monomers per polymer unit derived from maleic anhydride, which has been hydrolyzed in the presence of an alkali metal hydroxide or ammonium hydroxide and which has a number average molecular weight in the range between about 500 and 4000.
2. The substrate of Claim 1 wherein said ethylenically unsaturated aromatic monomer can be represented by the formula wherein R is or or CH2=CH-CH2-;
R1 is H-, CH3- or ;
R2 is H- or CH3-;
R3 is H-or CH3O-;
R4 is H-, CH3-, or , and R3 plus R4 is -O-CH2-O-
R1 is H-, CH3- or ;
R2 is H- or CH3-;
R3 is H-or CH3O-;
R4 is H-, CH3-, or , and R3 plus R4 is -O-CH2-O-
3. The substrate of Claim 1 wherein said ethylenically unsaturated aromatic monomer is styrene.
4. The substrate of Claim 1 wherein said polymer contains about one polymer unit derived from maleic anhydride per polymer unit derived from one or more ethylenically unsaturated aromatic monomers.
5. The substrate of Claim 1 wherein said polymer contains about one polymer unit derived from maleic anhydride per polymer unit derived from styrene.
6. The substrate of Claim 1 wherein said polymer has been hydrolyzed in the presence of sodium hydroxide.
7. The substrate of Claim 6 wherein said polymer contains about one polymer unit derived from maleic anhydride per polymer unit derived from styrene.
8. A process for imparting stain-resistance to a textile substrate which comprises applying to said substrate an effective amount of a composition comprising a polymer containing between about one and two polymer units derived from one or more ethylenically unsaturated aromatic monomers per polymer unit derived from maleic anhydride, which has been hydrolyzed in the presence of an alkali metal hydroxide or ammonium hydroxide and which has a number average molecular weight in the range between about 500 and 4000.
9. The process of Claim 8 wherein said ethylenically unsaturated aromatic monomer can be represented by the formula R
wherein R is R1-CH=C- or CH2=CH-CH2-;
R1 is H-, CH3 or -;
R2 is H- or CH3-;
R3 is H-or CH3O-;
R4 is H-, CH3-, or , and R3 plus R4 is -O-CH2-O-
wherein R is R1-CH=C- or CH2=CH-CH2-;
R1 is H-, CH3 or -;
R2 is H- or CH3-;
R3 is H-or CH3O-;
R4 is H-, CH3-, or , and R3 plus R4 is -O-CH2-O-
10. The process of Claim 8 wherein said ethylenically unsaturated aromatic monomer is styrene.
11. The process of Claim 8 wherein said polymer contains about one polymer unit derived from maleic anhydride per polymer unit derived from one or more ethylenically unsaturated aromatic monomers.
12. The process of Claim 8 wherein said polymer contains about one polymer unit derived from maleic anhydride per polymer unit derived from styrene.
13. The process of Claim 8 wherein said polymer is hydrolyzed in the presence of sodium hydroxide.
14. The process of Claim 13 wherein said polymer contains about one polymer unit derived from maleic anhydride per polymer unit derived from styrene.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13603887A | 1987-12-21 | 1987-12-21 | |
| US136,038 | 1987-12-21 | ||
| US28040788A | 1988-12-06 | 1988-12-06 | |
| US280,407 | 1988-12-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1332684C true CA1332684C (en) | 1994-10-25 |
Family
ID=26833934
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000586056A Expired - Lifetime CA1332684C (en) | 1987-12-21 | 1988-12-15 | Stain-resistant aromatic/maleic anhydride polymers |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP0329899B1 (en) |
| JP (1) | JP2632990B2 (en) |
| KR (1) | KR920006476B1 (en) |
| AT (1) | ATE116389T1 (en) |
| AU (1) | AU617731B2 (en) |
| CA (1) | CA1332684C (en) |
| DE (1) | DE3852627T2 (en) |
| DK (1) | DK709888A (en) |
| FI (1) | FI885889A (en) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU615242B2 (en) * | 1987-12-21 | 1991-09-26 | E.I. Du Pont De Nemours And Company | Stain-resistant agents for textiles |
| AU627711B2 (en) * | 1988-03-11 | 1992-09-03 | Minnesota Mining And Manufacturing Company | Process for providing polyamide materials with stain resistance |
| US5310828A (en) * | 1989-04-20 | 1994-05-10 | Peach State Labs, Inc. | Superior stain resistant compositions |
| US4940757A (en) * | 1989-04-20 | 1990-07-10 | Peach State Labs, Inc. | Stain resistant polymeric composition |
| US5223340A (en) * | 1989-04-20 | 1993-06-29 | Peach State Labs, Inc. | Stain resistant polyamide fibers |
| US5061763A (en) * | 1989-04-20 | 1991-10-29 | Peach State Labs, Inc. | Stain resistant treatment for polyamide fibers |
| US5015259A (en) * | 1989-04-20 | 1991-05-14 | Peach State Labs, Inc. | Stain resistant polymeric composition |
| US5135774A (en) * | 1990-03-27 | 1992-08-04 | Allied-Signal Inc. | Method to impart coffee stain resistance to polyamide fibers |
| US5118551A (en) * | 1990-03-27 | 1992-06-02 | Allied-Signal Inc. | Method to impart stain resistance to polyamide textile substrates |
| WO1992007131A1 (en) * | 1990-10-18 | 1992-04-30 | E.I. Du Pont De Nemours And Company | Stain-resistant sulfonated aromatic polymers |
| JPH06503386A (en) * | 1990-12-13 | 1994-04-14 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Maleic anhydride/olefin polymer stain resist |
| US5707708A (en) * | 1990-12-13 | 1998-01-13 | E. I. Du Pont De Nemours And Company | Maleic anhydride/olefin polymer stain-resists |
| EP0564591B1 (en) * | 1990-12-27 | 1995-05-24 | E.I. Du Pont De Nemours And Company | Maleic anhydride/vinyl or allyl ether polymer stain-resists |
| US5232743A (en) * | 1991-02-01 | 1993-08-03 | Allied-Signal Inc. | Method and composition to enhance acid dye stain resistance of polyamides by improving resistance to detergent washings and products thereof |
| US5232760A (en) * | 1991-02-01 | 1993-08-03 | Allied Signal Inc. | Method and composition to enhance acid dye stain resistance of polyamides by improving resistance to detergent washings and products thereof |
| EP0593617B1 (en) * | 1991-07-10 | 1996-05-08 | Minnesota Mining And Manufacturing Company | Fluorochemical water- and oil- repellent treating compositions |
| US5252232A (en) * | 1991-09-20 | 1993-10-12 | E. I. Du Pont De Nemours And Company | Stain and soil resistant compositions having freeze-thaw stability |
| US5236464A (en) * | 1991-12-16 | 1993-08-17 | Allied-Signal Inc. | Activation of nylon fibers for modification by UV radiation |
| MX9301644A (en) * | 1992-03-25 | 1993-09-01 | Du Pont | FIBROUS SUBSTRATE OF POLYAMIDE, COMPOSITION AND PROCESS TO PROVIDE RESISTANCE TO DISCOLORATION TO SUCH SUBSTRATE. |
| AU6026994A (en) * | 1993-02-02 | 1994-08-29 | E.I. Du Pont De Nemours And Company | Durable hydrolized maleic anhydride polymer stain-resists |
| US5520962A (en) * | 1995-02-13 | 1996-05-28 | Shaw Industries, Inc. | Method and composition for increasing repellency on carpet and carpet yarn |
| JP3819034B2 (en) * | 1996-02-23 | 2006-09-06 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Polymer / resole resin antifouling agent containing carboxylic acid |
| US5712348A (en) * | 1996-03-13 | 1998-01-27 | E. I. Du Pont De Nemours And Company | Maleic acid copolymers with fluorinated thioether end-cap |
| FR2805288A1 (en) * | 2000-02-23 | 2001-08-24 | Atofina | Composition for imparting soil-, solvent- and oil-repellency to carpets, comprises an aqueous solution of a carboxy-functional polymer and a cationic emulsion of a fluorinated copolymer |
| US6524492B2 (en) | 2000-12-28 | 2003-02-25 | Peach State Labs, Inc. | Composition and method for increasing water and oil repellency of textiles and carpet |
| US7335234B2 (en) | 2002-10-16 | 2008-02-26 | Columbia Insurance Company | Method of treating fibers, carpet yarns and carpets to enhance repellency |
| JP6213132B2 (en) * | 2013-10-11 | 2017-10-18 | 東ソー株式会社 | trans-stilbene-maleic anhydride copolymer and retardation film using the same |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE759066A (en) * | 1969-11-17 | 1971-05-17 | Atlantic Richfield Co | SHAMPOO COMPOSITIONS |
| DE2340879A1 (en) * | 1973-08-13 | 1975-03-13 | Hoechst Ag | PROCESS AND MEANS FOR FINISHING TEXTILES |
| US4144026A (en) * | 1976-07-06 | 1979-03-13 | Ciba-Geigy Corporation | Process for simultaneously providing synthetic textile materials with an antistatic and dirt-repellent finish |
| JPS5319492A (en) * | 1976-08-02 | 1978-02-22 | Kao Corp | Size agent component |
-
1988
- 1988-12-12 KR KR1019880016606A patent/KR920006476B1/en not_active IP Right Cessation
- 1988-12-14 AT AT88311835T patent/ATE116389T1/en not_active IP Right Cessation
- 1988-12-14 DE DE3852627T patent/DE3852627T2/en not_active Expired - Lifetime
- 1988-12-14 EP EP88311835A patent/EP0329899B1/en not_active Expired - Lifetime
- 1988-12-15 CA CA000586056A patent/CA1332684C/en not_active Expired - Lifetime
- 1988-12-20 AU AU27089/88A patent/AU617731B2/en not_active Expired
- 1988-12-20 FI FI885889A patent/FI885889A/en not_active Application Discontinuation
- 1988-12-20 DK DK709888A patent/DK709888A/en not_active Application Discontinuation
- 1988-12-21 JP JP63323212A patent/JP2632990B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| AU2708988A (en) | 1989-06-15 |
| EP0329899A2 (en) | 1989-08-30 |
| ATE116389T1 (en) | 1995-01-15 |
| DE3852627T2 (en) | 1995-06-08 |
| FI885889A (en) | 1989-06-22 |
| EP0329899A3 (en) | 1989-10-18 |
| AU617731B2 (en) | 1991-12-05 |
| JP2632990B2 (en) | 1997-07-23 |
| DK709888A (en) | 1989-06-22 |
| KR890010353A (en) | 1989-08-08 |
| DK709888D0 (en) | 1988-12-20 |
| EP0329899B1 (en) | 1994-12-28 |
| KR920006476B1 (en) | 1992-08-07 |
| JPH02138365A (en) | 1990-05-28 |
| DE3852627D1 (en) | 1995-02-09 |
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