US3497380A - Oil absorbent,oil resistant impregnated paper - Google Patents

Oil absorbent,oil resistant impregnated paper Download PDF

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US3497380A
US3497380A US596228A US3497380DA US3497380A US 3497380 A US3497380 A US 3497380A US 596228 A US596228 A US 596228A US 3497380D A US3497380D A US 3497380DA US 3497380 A US3497380 A US 3497380A
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oil
epoxy
impregnated
butadiene
styrene
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US596228A
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Robert E Weber
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Kimberly Clark Corp
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Kimberly Clark Corp
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    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/34Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/41Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
    • D21H17/42Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups anionic
    • D21H17/43Carboxyl groups or derivatives thereof

Definitions

  • Paper is commonly impregnated with elastomeric materials for a variety of purposes.
  • One such representative purpose is as a base sheet in a pressure sensitive tape.
  • the impregnated sheet serves the purpose of providing strength to the tape composite.
  • the elastomeric impregnated material is commonly cured.
  • Known impregnants for such base sheets which are subject to curing include terpolymer materials such as styrene-butadiene compositions having functional groups which include active hydrogen or the like.
  • a common deficiency of such elastomer saturated papers is that the necessary curing action not only improves the strength but it decreases the flexibility and stretch properties of the material.
  • such materials as the terpolymer compositions noted are not normally resistant to attack by organic solvents.
  • the above noted objects of this invention may be achieved.
  • the product is oil resistant and through, in fact, it may absorb some significant quantity of oil and undergo some slight swelling, it will not disintegrate mechanically.
  • the epoxy apparently serves as a cross-linking agent for the styrene-butadiene terpolymer and would be expected to render the product relatively rigid, the stretch characteristics and flexibility of the cured impregnated mate rial are, in fact, similar to those of the uncured sheet.
  • the styrene-butadiene employed in the practice of the invention is a common type but characterized by the presence of functional hydrogen.
  • Carboxylic styrenebutadiene is one terpolymer which serves the purpose and may be formulated with styrene, butadiene and acrylic acid. While it is convenient to employ the carboxylic styrene-butadiene since they are readily commercially available polymers of styrene-butadiene having active bydrogens, other systems with active hydrogen may be employed. Such include as functional groups the amines and amides.
  • terpolymers of carboxylic styrene-butadiene in which the styrene is present (dry basis by weight) between about 20 to 40%, the acid 1 to 3%, and butadiene is the remainder.
  • Epoxy resins which I prefer to employ are those which are of a relatively low molecular weight and dispersible in water or readily emulsifiable.
  • Epoxy resins which serve the purpose well include the di-epoxides, for example, which are commercially available colorless to pale liquids having a viscosity of about to 150 centipoises at 25 C., a neutral pH and a gallon weight of about 10.2 pounds.
  • Higher molecular weight resins may be conveniently dispersed in solvents prior to their emulsification and, accordingly, both liquid and solid type materials are useful.
  • One commercially available resin having an epoxide equivalent at about 185-192 and an average molecular weight of about 380 and which is readily dispersible in hydrocarbon solvents such as toluene and xylene is also useful for the purpose.
  • the following example provides comparative data on materials produced with from zero to 5% epoxy (dry weight percent based on rubber dry weight).
  • the cellulose web for the comparative purpose comprised a saturating base sheet of essentially kraft pulp. This base sheet was impregnated with the combined emulsion system formed as described below. After impregnation, as by dipping in the emulsion, the web was then squeezed to a pickup on a dry basis of 45 parts of the impregnant per 100 parts by weight of base sheet.
  • Emulsion A A first emulsion was made up in conventional fashion and is here conveniently termed Emulsion A. This emulsion was a commercial material and as purchased contained on a solids basis:
  • a second aqueous emulsion was prepared from a bifunctional epoxy resin and a non-ionic emulsifier, in this case polyoxyethylene sorbitan trioleate.
  • the epoxy resin is the dispersed phase.
  • the aqueous or continuous phase may include only water but, if desired, other components such as antioxidants, emulsion stabilizers and viscosity control agents may be included, for saturant stability.
  • the emulsion contain an epoxy resin with an epoxide equivalent of about and a density of 1.2 gm./cm.
  • Emulsion B This second emulsion, conveniently termed Emulsion B, was prepared as follows:
  • Curing time is inversely related to temperature, and the system has been cured at temperatures of between about 70 F. and 300 F.
  • the cured impregnated base sheets were tested and compared with a similar base sheet lacking the epoxy resin by subjecting the sheets to a liquid hydrocarbon as follows: strips were saturated with motor oil (20 A.S.E.) and tested on an Instron tester, the rate of elongation being 4% /min.
  • the epoxy inclusion appears particularly effective in the low ranges. Frequently 0.5 to 1% dry weight based on the rubber is sufficient for the purpose. I have found that between about A2 part to 5 parts by weight per 100 parts of dry rubber is generally useful and more than 5 parts is not commonly necessary or economical. Additionally, I have found that the physical characteristics of sheets varying in epoxy content but not subjected to oil vary but little in tensile, stretch and the like. It is when subjected to the oil that the effects of the epoxy inclusion are noted. The physical properties of the product will vary somewhat, of course, with the degree of impregnationmost suitably, the impregnant by weight is present to the extent of about 30 to 120 parts per 100 parts of fiber.
  • the sheets whether or not they contain the epoxy, will tend, because of their structure and porosity, to absorb oil. This is occasioned by the very low density and the exposed rubber covered, substantially individual fibers.
  • the presence of the epoxy precludes the disintegration of the impregnated sheet with oil absorption because the rubber is much less swollen by a given amount of oil absorbed and the oil in the latter case is simply retained in the pores of the sheet.
  • the products, in accordance with the invention, are thus characterized by a relatively low density and high porosity.
  • An exemplary density in accordance with the example set out hereinbefore is about 0.5 gram per cubic centimeter or a pore volume of the'sheet of about 60%.
  • Such light weight and porosity is of advantage particularly when accompanied by the flexibility of the product in the use of the material as supported absorbent pads in single or multi-ply.
  • the material may be retained by a wire mesh or the like and positioned in proximity to the source of an oilleak, forthe purpose of picking up the oil drippings, etc.
  • the impregnated product is capable of use in areas commonly subject to the presence of considerable quantities of oil and may pick up two to three times its own weight of motor oil without disintegration.
  • a product in accordance with this invention might be used as a mat in a tool room or garage, or may serve as an oil resistant gasket or the like.
  • An oil resistant, flexible, absorbent paper fiber product which is capable of absorbing two to three times its own weight of motor oil without disintegration comprising a paper web having a strengthening impregnant present to the extent of between about 30 to 120 parts per parts by weight of fiber and which impregnant is the reaction product of an epoxy resin and a terpolymer consisting essentially of styrene-butadiene polymer having functional hydrogen wherein the styrene is present in the polymer on a dry weight basis to the extent of between about 20-40%, the component having the functional hydrogen is present to the extent of about 1-3%, and the butadiene constitutes the remainder, and the epoxy is present to the extent of between about /2 part to 5 parts per 100 parts of the styrene-butadiene impregnant also on a dry weight basis.
  • a paper product according to claim 1 wherein the impregnant is the reaction product of the polymer and between about 0.5 to 1% of epoxy on a dry weight basis.

Description

Feb. 24', 1910' 01L ABSORBENT;
' R. E} WEBER OILRESISTANT IMPREGNATED PAPER Filed NOV. 22, 1966 IMPREGNATED WITH OIL RESISTANT TERPOLYMER United States Patent Ofiice 3,497,380 Patented Feb. 24, 1970 3,497,380 OIL ABSORBENT, OIL RESISTANT IMPREGNATED PAPER Robert E. Weber, Neenah, Wis., assignor to Kimberly- Clark Corporation, Neenah, Wis., a corporation of Delaware Filed Nov. 22, 1966, Ser. No. 596,228
Int. Cl. C08c 17/18; -C08d 13/18 U.S. Cl. 117155 2 Claims ABSTRACT OF THE DISCLOSURE This invention relates to elastomer saturated paper and particularly to methods of producing such papers having good flexibility and stretch properties as well as resistance to deterioration by organic solvents including attack by hydrocarbons.
Paper is commonly impregnated with elastomeric materials for a variety of purposes. One such representative purpose is as a base sheet in a pressure sensitive tape. In such tapes the impregnated sheet serves the purpose of providing strength to the tape composite. The elastomeric impregnated material is commonly cured. Known impregnants for such base sheets which are subject to curing include terpolymer materials such as styrene-butadiene compositions having functional groups which include active hydrogen or the like. A common deficiency of such elastomer saturated papers is that the necessary curing action not only improves the strength but it decreases the flexibility and stretch properties of the material. Furthermore, such materials as the terpolymer compositions noted are not normally resistant to attack by organic solvents.
It is a purpose of this invention to provide an impregnated paper web in which the strengthening impreg nant of the web is a terpolymer and which impregnated web demonstrates a material resistance to attack by hydrocarbons including oils and solvents such as xylene, toluene and the like. It is another object of this invention to provide a novel method of impregnating a cellulosic web to attain desirable physical characteristics in the product by the inclusion in the impregnant of only a very minor quantity of an epoxy type resin serving basically as a curing agent.
I have found that, if a small percentage of an epoxy resin is included in the elastomeric formulation for the impregnation of a cellulosic web, the above noted objects of this invention may be achieved. Specifically, the product is oil resistant and through, in fact, it may absorb some significant quantity of oil and undergo some slight swelling, it will not disintegrate mechanically. Additionally and quite surprisingly, despite the fact that the epoxy apparently serves as a cross-linking agent for the styrene-butadiene terpolymer and would be expected to render the product relatively rigid, the stretch characteristics and flexibility of the cured impregnated mate rial are, in fact, similar to those of the uncured sheet.
The styrene-butadiene employed in the practice of the invention is a common type but characterized by the presence of functional hydrogen. Carboxylic styrenebutadiene is one terpolymer which serves the purpose and may be formulated with styrene, butadiene and acrylic acid. While it is convenient to employ the carboxylic styrene-butadiene since they are readily commercially available polymers of styrene-butadiene having active bydrogens, other systems with active hydrogen may be employed. Such include as functional groups the amines and amides. Commonly, I prefer to employ terpolymers of carboxylic styrene-butadiene in which the styrene is present (dry basis by weight) between about 20 to 40%, the acid 1 to 3%, and butadiene is the remainder.
The epoxy resins which I prefer to employ are those which are of a relatively low molecular weight and dispersible in water or readily emulsifiable. Epoxy resins which serve the purpose well include the di-epoxides, for example, which are commercially available colorless to pale liquids having a viscosity of about to 150 centipoises at 25 C., a neutral pH and a gallon weight of about 10.2 pounds. Higher molecular weight resins may be conveniently dispersed in solvents prior to their emulsification and, accordingly, both liquid and solid type materials are useful. One commercially available resin having an epoxide equivalent at about 185-192 and an average molecular weight of about 380 and which is readily dispersible in hydrocarbon solvents such as toluene and xylene is also useful for the purpose.
The invention will be more fully understood by reference to the following example and accompanying drawing wherein the single figure is a sectional view illustrating a base sheet impregnated in accordance with the invention.
The following example provides comparative data on materials produced with from zero to 5% epoxy (dry weight percent based on rubber dry weight).
The cellulose web for the comparative purpose comprised a saturating base sheet of essentially kraft pulp. This base sheet was impregnated with the combined emulsion system formed as described below. After impregnation, as by dipping in the emulsion, the web was then squeezed to a pickup on a dry basis of 45 parts of the impregnant per 100 parts by weight of base sheet.
A first emulsion was made up in conventional fashion and is here conveniently termed Emulsion A. This emulsion was a commercial material and as purchased contained on a solids basis:
Percent Butadiene 72 Styrene 25 Acrylic acid 3 A second aqueous emulsion was prepared from a bifunctional epoxy resin and a non-ionic emulsifier, in this case polyoxyethylene sorbitan trioleate. The epoxy resin is the dispersed phase. The aqueous or continuous phase may include only water but, if desired, other components such as antioxidants, emulsion stabilizers and viscosity control agents may be included, for saturant stability. In the present instance the emulsion contain an epoxy resin with an epoxide equivalent of about and a density of 1.2 gm./cm.
This second emulsion, conveniently termed Emulsion B, was prepared as follows:
Parts Epoxy resin 20 Polyoxyethylene sorbitan trioleate 1 Water 100 Such components are emulsified with an Eppon bach mixer. When emulsification had been completed, the epoxy emulsionEmulsion Bwas added to styrene-butadiene emulsionEmulsion Ain three different proportions having a dry weight ratio of rubber to resin of 100:0.5;
100:1; and 100:5 respectively. After dipping and squeezing, as already noted, cure of these low density impregnated cellulose webs waseffected in an oven at about 115 C. (239 F.) for three hours. In all cases the rubber to cellulose ratio was 45:100.
Curing time is inversely related to temperature, and the system has been cured at temperatures of between about 70 F. and 300 F.
The cured impregnated base sheets were tested and compared with a similar base sheet lacking the epoxy resin by subjecting the sheets to a liquid hydrocarbon as follows: strips were saturated with motor oil (20 A.S.E.) and tested on an Instron tester, the rate of elongation being 4% /min.
As will be noted from the foregoing exemplary data, the epoxy inclusion appears particularly effective in the low ranges. Frequently 0.5 to 1% dry weight based on the rubber is sufficient for the purpose. I have found that between about A2 part to 5 parts by weight per 100 parts of dry rubber is generally useful and more than 5 parts is not commonly necessary or economical. Additionally, I have found that the physical characteristics of sheets varying in epoxy content but not subjected to oil vary but little in tensile, stretch and the like. It is when subjected to the oil that the effects of the epoxy inclusion are noted. The physical properties of the product will vary somewhat, of course, with the degree of impregnationmost suitably, the impregnant by weight is present to the extent of about 30 to 120 parts per 100 parts of fiber. But varying the impregnation does not contribute to the product in the same manner as the epoxy. In brief, the sheets, whether or not they contain the epoxy, will tend, because of their structure and porosity, to absorb oil. This is occasioned by the very low density and the exposed rubber covered, substantially individual fibers. The presence of the epoxy, however, precludes the disintegration of the impregnated sheet with oil absorption because the rubber is much less swollen by a given amount of oil absorbed and the oil in the latter case is simply retained in the pores of the sheet.
The products, in accordance with the invention, are thus characterized by a relatively low density and high porosity. An exemplary density in accordance with the example set out hereinbefore is about 0.5 gram per cubic centimeter or a pore volume of the'sheet of about 60%. Such light weight and porosity is of advantage particularly when accompanied by the flexibility of the product in the use of the material as supported absorbent pads in single or multi-ply. For example, the material may be retained by a wire mesh or the like and positioned in proximity to the source of an oilleak, forthe purpose of picking up the oil drippings, etc.
Because of the noted characteristics of strength, flexibility, good stretch properties and resistance to oil, the impregnated product is capable of use in areas commonly subject to the presence of considerable quantities of oil and may pick up two to three times its own weight of motor oil without disintegration. For example, a product in accordance with this invention might be used as a mat in a tool room or garage, or may serve as an oil resistant gasket or the like.
As many apparently widely different embodiments of this invention may be made without departing from the spirit and scope thereof, it is to be understood that I do not limit myself to the specific embodiments thereof.
What is claimed is:
1. An oil resistant, flexible, absorbent paper fiber product which is capable of absorbing two to three times its own weight of motor oil without disintegration comprising a paper web having a strengthening impregnant present to the extent of between about 30 to 120 parts per parts by weight of fiber and which impregnant is the reaction product of an epoxy resin and a terpolymer consisting essentially of styrene-butadiene polymer having functional hydrogen wherein the styrene is present in the polymer on a dry weight basis to the extent of between about 20-40%, the component having the functional hydrogen is present to the extent of about 1-3%, and the butadiene constitutes the remainder, and the epoxy is present to the extent of between about /2 part to 5 parts per 100 parts of the styrene-butadiene impregnant also on a dry weight basis.
2. A paper product according to claim 1 wherein the impregnant is the reaction product of the polymer and between about 0.5 to 1% of epoxy on a dry weight basis.
References Cited UNITED STATES PATENTS 2,791,520 5/1957 Gerke et al. 117-138.8 X 2,824,851 2/1958 Hall.
2,947,338 8/1960 Reid et al.
3,011,882 12/1961 Quinan et al. 117161 X 3,019,134 1/1962 Hechtman et al. l17-155 3,026,217 3/1962 Hechtman et al. 117---155 3,027,337 3/1962 Tritsch 117-161 X 3,055,496 9/1962 Dunlap 162168 X 3,308,007 3/1967 Shepard 1l776 X 3,309,224 3/1967 Weber 117155 3,345,204 10/1967 Dunlap 117155 X FOREIGN PATENTS 788,381 1/1958 Great Britain.
WILLIAM D. MARTIN, Primary Examiner M. R. LUSIGNAN, Assistant Examiner
US596228A 1966-11-22 1966-11-22 Oil absorbent,oil resistant impregnated paper Expired - Lifetime US3497380A (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3637431A (en) * 1968-09-30 1972-01-25 Little Inc A Coating composition and article coated with same
US3944125A (en) * 1974-10-09 1976-03-16 Jack Friedman Container
US5002982A (en) * 1990-02-26 1991-03-26 Gencorp Inc. Paper felts or mats
US5523345A (en) * 1994-02-25 1996-06-04 Gencorp Inc. Latex binder compositions

Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2791520A (en) * 1955-05-18 1957-05-07 Us Rubber Co Textile article coated with terpolymer of butadiene, acrylonitrile, and methacrylic acid
GB788381A (en) * 1955-04-07 1958-01-02 Bataafsche Petroleum Compositions containing epoxy compounds for treating synthetic fibres
US2824851A (en) * 1953-08-24 1958-02-25 Minnesota Mining & Mfg Acrylic acid derivatives of epoxide resins and method of curing same
US2947338A (en) * 1957-04-19 1960-08-02 Firestone Tire & Rubber Co Epoxide cure of rubbery copolymer which contains a reactive carboxyl group
US3011882A (en) * 1958-02-27 1961-12-05 Norton Co Coated abrasives
US3019134A (en) * 1958-09-10 1962-01-30 Kimberly Clark Co Cellulosic product
US3026217A (en) * 1958-04-11 1962-03-20 Kimberly Clark Co Fiber products and methods of manufacturing comprising base sheet of cellulose fibers saturated with a mixture comprising elastomeric polymer and polar adjunct polymer having carboxylic acid functional group
US3027337A (en) * 1959-05-18 1962-03-27 Kendall & Co Pressure-sensitive adhesives and tapes containing same, said adhesive comprising a rubber, a tackifying resin and an epoxy compound
US3055496A (en) * 1956-11-23 1962-09-25 Johnson & Johnson Unified paper sheet, process of making, and pressure-sensitive adhesive tape made therefrom
US3308007A (en) * 1963-05-06 1967-03-07 Du Pont Treatment for improving adhesion of fibrous material to rubber
US3309224A (en) * 1963-03-07 1967-03-14 Kimberly Clark Co Method of coating paper with pigmented protein containing oil-in-water emulsions having epoxy resin dispersed in oil phase
US3345204A (en) * 1963-06-06 1967-10-03 Johnson & Johnson Process of impregnating an instantaneously wettable paper with a rubber latex

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2824851A (en) * 1953-08-24 1958-02-25 Minnesota Mining & Mfg Acrylic acid derivatives of epoxide resins and method of curing same
GB788381A (en) * 1955-04-07 1958-01-02 Bataafsche Petroleum Compositions containing epoxy compounds for treating synthetic fibres
US2791520A (en) * 1955-05-18 1957-05-07 Us Rubber Co Textile article coated with terpolymer of butadiene, acrylonitrile, and methacrylic acid
US3055496A (en) * 1956-11-23 1962-09-25 Johnson & Johnson Unified paper sheet, process of making, and pressure-sensitive adhesive tape made therefrom
US2947338A (en) * 1957-04-19 1960-08-02 Firestone Tire & Rubber Co Epoxide cure of rubbery copolymer which contains a reactive carboxyl group
US3011882A (en) * 1958-02-27 1961-12-05 Norton Co Coated abrasives
US3026217A (en) * 1958-04-11 1962-03-20 Kimberly Clark Co Fiber products and methods of manufacturing comprising base sheet of cellulose fibers saturated with a mixture comprising elastomeric polymer and polar adjunct polymer having carboxylic acid functional group
US3019134A (en) * 1958-09-10 1962-01-30 Kimberly Clark Co Cellulosic product
US3027337A (en) * 1959-05-18 1962-03-27 Kendall & Co Pressure-sensitive adhesives and tapes containing same, said adhesive comprising a rubber, a tackifying resin and an epoxy compound
US3309224A (en) * 1963-03-07 1967-03-14 Kimberly Clark Co Method of coating paper with pigmented protein containing oil-in-water emulsions having epoxy resin dispersed in oil phase
US3308007A (en) * 1963-05-06 1967-03-07 Du Pont Treatment for improving adhesion of fibrous material to rubber
US3345204A (en) * 1963-06-06 1967-10-03 Johnson & Johnson Process of impregnating an instantaneously wettable paper with a rubber latex

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3637431A (en) * 1968-09-30 1972-01-25 Little Inc A Coating composition and article coated with same
US3944125A (en) * 1974-10-09 1976-03-16 Jack Friedman Container
US5002982A (en) * 1990-02-26 1991-03-26 Gencorp Inc. Paper felts or mats
US5523345A (en) * 1994-02-25 1996-06-04 Gencorp Inc. Latex binder compositions
US5623015A (en) * 1994-02-25 1997-04-22 Gencorp Inc. Latex binder compositions

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