US3344016A - Method of making beater-saturated water-laid product containing paper-making and textile staple fibers - Google Patents

Method of making beater-saturated water-laid product containing paper-making and textile staple fibers Download PDF

Info

Publication number
US3344016A
US3344016A US442481A US44248165A US3344016A US 3344016 A US3344016 A US 3344016A US 442481 A US442481 A US 442481A US 44248165 A US44248165 A US 44248165A US 3344016 A US3344016 A US 3344016A
Authority
US
United States
Prior art keywords
slurry
fibers
water
weight
salt
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.)
Expired - Lifetime
Application number
US442481A
Inventor
William A Moggio
John M Lesniak
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Armstrong World Industries Inc
Original Assignee
Armstrong Cork Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Armstrong Cork Co filed Critical Armstrong Cork Co
Priority to US442481A priority Critical patent/US3344016A/en
Application granted granted Critical
Publication of US3344016A publication Critical patent/US3344016A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • D21H17/35Polyalkenes, e.g. polystyrene
    • 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
    • D21H13/00Pulp or paper, comprising synthetic cellulose or non-cellulose fibres or web-forming material
    • D21H13/10Organic non-cellulose fibres
    • 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
    • D21H13/00Pulp or paper, comprising synthetic cellulose or non-cellulose fibres or web-forming material
    • D21H13/36Inorganic fibres or flakes
    • D21H13/38Inorganic fibres or flakes siliceous
    • D21H13/40Inorganic fibres or flakes siliceous vitreous, e.g. mineral wool, glass fibres
    • 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
    • D21H13/00Pulp or paper, comprising synthetic cellulose or non-cellulose fibres or web-forming material
    • D21H13/36Inorganic fibres or flakes
    • D21H13/38Inorganic fibres or flakes siliceous
    • D21H13/42Asbestos
    • 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
    • D21H17/63Inorganic compounds
    • D21H17/66Salts, e.g. alums
    • 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
    • D21H23/00Processes or apparatus for adding material to the pulp or to the paper
    • D21H23/02Processes or apparatus for adding material to the pulp or to the paper characterised by the manner in which substances are added
    • D21H23/04Addition to the pulp; After-treatment of added substances in the pulp
    • D21H23/06Controlling the addition
    • D21H23/08Controlling the addition by measuring pulp properties, e.g. zeta potential, pH
    • D21H23/10Controlling the addition by measuring pulp properties, e.g. zeta potential, pH at least two kinds of compounds being added

Definitions

  • the present process contemplates forming in water a slurry of papermaking fibers, and adding to the slurry an alum solution. After agitation, the alumtreated slurry is neutralized with alkali to a pH in the range of 6 to 8, preferably 7. To the neutralized slurry there is then added a rubber latex in an amount of 200%650% by weight dry rubber solids based on the dry weight of the papermaking fibers. There is then added, in indifferent order, long staple fibers in an amount of 50%900% by dry weight based on the dry weight of the papermaking fibers, and a water-soluble salt of a metal in Group I, II, IV, VII, or VIII of the Periodic Table.
  • alkali is added to achieve a. pH in the range of 8.51 to 1.5 to form an insoluble hydroxide with the metal ion from the salt.
  • a sheet may then be formed from the resulting slurry, and the sheet will possess textile-like characteristics.
  • the papermaking fibers to be used in the present process are the known papermaking fibers such as asbestos, glass, mineral wool, animal hair, leather, as well as the cellulosic fibers such as kraft, rag stock, soda, semi-chemical, ground-wood, sulfite stock, alpha pulp, cotton linters, jute, hemp, sisal, strings, chopped canvas, and other such fibers, which may be bleached, semi-bleached, or unbleached.
  • the fibers will be formed into a papermaking slurry by known processes of beating or otherwise refining the fibers in an aqueous medium.
  • the fibers may then be treated by the alum-ammonia process described in US. 2,375,245-Pretzel, or more preferably, by a modification thereof which may be referred to as the alum-caustic process.
  • the refined fibers in water are treated with a solution of alum, preferably papermakers alum.
  • the solution of aluminum sulfate is simply poured into the slurry with agitation.
  • the amount of alum to be used may be varied somewhat but will generally lie within the range of 1 to- 6 parts by weight alum per 1 part by dry weight of the fiber to be treated.
  • alkali will be added to the alum-treated slurry to bring the pH up to a range of 68, preferably 7.
  • ammonium hydroxide may be used for such treatment, it is preferred to use an alkali metal hydroxide "ice such as potassium hydroxide, and preferably, sodium hydroxide.
  • ice such as potassium hydroxide, and preferably, sodium hydroxide.
  • the addition of the alkali to achieve the stated pH will produce aluminum hydroxide, much of which deposits on the fibers themselves. Some aluminum hydroxide, may remain suspended in the water. The quantity in the water is dependent on the alum to fiber ratio.
  • the neutralized slurry is then ready for the addition of the synthetic rubber binder.
  • binders are those normally contemplated for use in the beater saturation processes.
  • Typical of these synthetic rubbers are the butadiene-styrene copolymers (SBR) often containing 30-80% by weight butadiene.
  • SBR butadiene-styrene copolymers
  • High styrene butadiene-styrene copolymers may also be used, although the tackiness characteristic of the lower styrene content is preferred in the binder solids.
  • butadiene-acrylonitrile copolymers normally containing 50%80% by weight butadiene, the neoprenes (polychloroprenes), the homopolymers of butadiene as well as homopolyrners and/ or copolymers of butadiene homologs such as isoprene all can be used as binders in the present system; the so-called butyl rubber latices are useful.
  • the synthetic rubber latex will simply be added to the neutralized slurry in the requisite amount.
  • relatively huge amounts of rubber binder are necessary, based on the dry weight of the papermaking fibers. Therefore, an amount of synthetic rubber latex binder will be added to achieve a dry rubber solids content of 200%650% by weight based on the dry weight of the papermaking fibers.
  • Such a large amount of rubber solids has normally been avoided in the beater saturation arts in the past since it is almost unavoidable to precipitate some of the rubber solids in the water rather than on the fibers.
  • the slurry is in condition to receive the staple synthetic fibers or other fibers and the water-soluble metal salt.
  • the uncoated fibers will normally have a length in the range of inch to 1 inch and are added to the slurry of rubber-coated papermaking fibers in an amount of 50%900% by weight based on the dry weight of the papermaking fibers themselves.
  • the usual agitation sufiices to distribute the staple fibers throughout the slurry.
  • These staple fibers may be synthetic fibers such as rayon, acetate, polyamide fibers, polyester fibers, poly(vinyl chloride) fibers, and other hard-to-handle fibers as far as beater saturation is concerned.
  • the water-soluble salt will then be added, if it has not been added prior to the addition of the staple fibers. It makes little difference in the process if the uncoated fiber or the water-soluble salt is first added to the slurry of coated fibers.
  • These Water-soluble salts are those which result from the reaction of acetic acid or the inorganic mineral acids with the proper metallic compound.
  • the inorganic mineral acids are typically hydrochloric acid, nitric acid, and sulfuric acid.
  • the metallic portionthe cationof the water-soluble salt to be added to the slurry will be any of the metals found in the groups of the Periodic system mentioned earlier.
  • Aluminum and chromium do not work in the control of processing characteristics of the slurry, probably because of the ease with which these two metals form anions with oxygen at an alkaline pH.
  • the metals which function in the present method appear to do so by virtue of the nature of their behavior after the salt-containing slurry has been made alkaline, to be described below.
  • Typical of the water-soluble salts Which operate in the present method are lead acetate, manganous chloride, ferrous chloride, ferric chloride, calcium chloride, cobalt chloride, nickel chloride, and the corresponding nitrates and water-soluble sulfates thereof.
  • the Water-soluble salts are preferably added in the form of their water solution, with agitation.
  • the maximum amount of the salt to be added to control the drainage characteristics is determined by the weight of the cation portion of the salt.
  • the weight of the cation portion of the salt should not exceed about 50% of weight of the uncoated fibers on a dry basis. Larger amounts of the salt are not only wasteful, but may impart a harshness of hand to the finished sheet. As to the minimum amount of salt to be added, quite small amounts are effective. Activity of the different operable water-soluble salts will differ, but a reasonable minimum may be established at about 0.1% by weight of the cation portion of the salt based on the weight of the uncoated fibers.
  • a dilute solution on the order of 1%5% by Weight of the salt in water. This solution will be added with agitation in order to distribute the water-soluble salt thoroughly throughout the slurry.
  • ammonium hydroxide, sodium hydroxide, or potassium hydroxide may be used, ammonium hydroxide may form soluble complexes with some of the metals used in making the water-soluble metal salt. Potassium hydroxide is comparatively expensive. For these reasons, sodium hy- Weight and Type of Papermoking Fiber Weight and Type of Staple Fiber in redients will be known and occasional checks may be all that is required.
  • the final slurry with its pH of about 9.5, is ready for dewatering as soon as the caustic has been thoroughly admixed.
  • a product will be formed from the resulting slurry by removing water therefrom as by introducing the agitated slurry onto a papermaking or feltmaking wire or cylinder.
  • the drainage characteristics of the particular finished slurry will be found to be controllable by the amount of water-soluble metal salt that has been added within the limits described above. Increased amounts of the water-soluble salt increase the drainage time and decrease the Canadian 3-gram freeness. In accordance with the present method then, it is possible to decide exactly the drainage characteristics desired of the slurry under preparation, and adjust the water-soluble metal salt addition accordingly.
  • the slurry will then be formed into a sheet in a papermaking wire or cylinder, or other device.
  • the sheet On drying, it will be found that the sheet has an extraordinary drape for a heater saturated, water-laid product, reminiscent of a textile.
  • the hand is soft and there is little or none of the harshness or brittleness normally associated with a paper or felt product.
  • the product does not crease in the normal sense of the word and, in some modifications, is surprisingly difiicult to tear with the fingers in thicknesses of about 0.02 inch.
  • this product may be used in place of woven cloth and has many applications such as doilies, tablecloths, and certain items of clothing.
  • Example 1 A series of runs was made in which one part by weight of a papermaking fiber was dispersed in 1,850 parts water, and the slurry was refined. There was then added 15 parts by volume of a 20% by weight aluminum sulfate solution with agitation. Sufiicient 10% sodium hydroxide solution was then added in each case to obtain a pH of 7.0. A synthetic rubber latex was then added with agitation. Following precipitation of the latex there was then added 8 parts by volume of a 1.2% by weight magnesium sulfate solution, followed by the addition of uncoated staple fiber, followed by the addition of sufficient 10% by weight sodium hydroxide solution to achieve a pH of 9.5. The following table illustrates the particular ingredients in the amounts used.
  • Binder 1 leather 1, asbestos 4 olyamide (nylon 3 4 inch) 6: poly amide (nylon: inch) 3, but-adlene-styrene copolyme. 5, butadiene-styrene copolyrnr. 3, butyl rubber. or
  • the caustic of choice is the caustic of choice.
  • the caustic will be added in the form of its water solution, the concentration being any convenient concentration, a 10% solution of the caustic being a good average.
  • Sufficient of the caustic solution is added with agitation to establish a pH within the above-mentioned pH range in the slurry, the target pH being 9.5.
  • a pH higher than about 11.5 may unduly harm or react with the ingredients in the slurry, while a pH below about 8.5 is not high enough to achieve the full desirable effects of the present method.
  • the pH of the resultant slurry may be checked in known manner with a suitable pH meter or test paper.
  • Each of the finished slurries described above was formed into a sheet measuring 0.020 inch thickness, dried at 220 F., and cooled. Each sheet was soft and flexible and possessed none of the harshness and brittleness of normal paper and felt products. Each sheet had the hand and drape of a textile product.
  • Example 2 Runs were made using 2 parts asbestos fibers in 1,850 parts water, followed by the usual alum-sodium hydroxduction of any particular product, the amounts of the ide treatment, followed by addition of 6 parts (dry basis) butadiene-styrene copolymer binder.
  • the precipitated slurry before treatment was unsuitable for forming a sheet product due to the large amount of precipitated fines which were lost with the white water.
  • the addition of caustic alone to a pH of 9.5 caused the formation of large clumps, again unsuitable for sheet formation.
  • the addition of a 1% solution of the metal salt indicated in the amount indicated improved the sheet formation as opposed to either the untreated slurry, or the caustic treated slurry in the absence of the metal salt.
  • the following table identifies the metal salt and the volume of 1% by weight solution used.
  • the method of forming a heater saturated, nonwoven textile substitute which comprises forming in water a slurry of papermaking fibers, adding alum to said slurry, adjusting the pH of the alum-treated slurry to a range of 6-8 by adding alkali thereto, adding a synthetic rubber latex in an amount of 200%650% by Weight dry rubber solids based on the dry weight of the papermaking fibers to the neutralized slurry whereby the solids content of the binder precipitates, adding to the resulting slurry in indifferent order long, staple fibers in an amount of %900% by weight based on the dry weight of the papermaking fibers and a water-soluble salt of a metal selected from the group consisting of metals in Groups I, II, IV, VII, and VIII of the Periodic Table, adding sufficient alkali to the salt-treated slurry containing said staple fibers to achieve a pH in the range of 8.511.5 to form an insoluble hydroxide with the metal ion from the salt, and forming
  • said alkali comprises sodium hydroxide.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Paper (AREA)

Description

United States Patent 3 344,016 METHQD 0F MAKIlhIG EEATER SATURATED WATER-LAID PRODUCT CONTAINING IA- PER-MAKING AND TEXTILE STAPLE FIBEIXS Wiliiam A. Moggio and John M. Lesniak, Millersville, Pa., assignors to Armstrong Cork Company, Lancaster, Pa., a corporation of Pennsylvania No Drawing. Filed Mar. 24, 1965, Ser. No. 442,481 9 Claims. (Cl. 16Z146) This invention relates generally to the production of a beater saturated fiber sheet product which resembles a woven textile. More particularly, the invention relates to a beater saturated product which has the hand, drape, and feel of a textile product as opposed to the normal harsh and brittle feel of a paper-like product.
In copending application Ser. No. 442,482, filed Mar. 24, 1965, there is described a process of controlling the drainage characteristics of slurries of beater saturated, rubber-coated fibers. That process in general calls for the addition of a water-soluble metallic salt to the fibrous slurry containing the precipitated rubber binder, followed by the addition of alkali to achieve an elevated pH. The present process utilizes that process but includes certain additional features necessary to produce a strong, soft, textile-like sheet product.
Accordingly, the present process contemplates forming in water a slurry of papermaking fibers, and adding to the slurry an alum solution. After agitation, the alumtreated slurry is neutralized with alkali to a pH in the range of 6 to 8, preferably 7. To the neutralized slurry there is then added a rubber latex in an amount of 200%650% by weight dry rubber solids based on the dry weight of the papermaking fibers. There is then added, in indifferent order, long staple fibers in an amount of 50%900% by dry weight based on the dry weight of the papermaking fibers, and a water-soluble salt of a metal in Group I, II, IV, VII, or VIII of the Periodic Table. After thorough mixing of the long staple fibers and the metal salt with the rubber-coated papermaking fibers, alkali is added to achieve a. pH in the range of 8.51 to 1.5 to form an insoluble hydroxide with the metal ion from the salt. A sheet may then be formed from the resulting slurry, and the sheet will possess textile-like characteristics.
The papermaking fibers to be used in the present process are the known papermaking fibers such as asbestos, glass, mineral wool, animal hair, leather, as well as the cellulosic fibers such as kraft, rag stock, soda, semi-chemical, ground-wood, sulfite stock, alpha pulp, cotton linters, jute, hemp, sisal, strings, chopped canvas, and other such fibers, which may be bleached, semi-bleached, or unbleached.
The fibers will be formed into a papermaking slurry by known processes of beating or otherwise refining the fibers in an aqueous medium.
The fibers may then be treated by the alum-ammonia process described in US. 2,375,245-Pretzel, or more preferably, by a modification thereof which may be referred to as the alum-caustic process. In this process, the refined fibers in water are treated with a solution of alum, preferably papermakers alum. The solution of aluminum sulfate is simply poured into the slurry with agitation. The amount of alum to be used may be varied somewhat but will generally lie within the range of 1 to- 6 parts by weight alum per 1 part by dry weight of the fiber to be treated.
After agitation, alkali will be added to the alum-treated slurry to bring the pH up to a range of 68, preferably 7. Although ammonium hydroxide may be used for such treatment, it is preferred to use an alkali metal hydroxide "ice such as potassium hydroxide, and preferably, sodium hydroxide. The addition of the alkali to achieve the stated pH will produce aluminum hydroxide, much of which deposits on the fibers themselves. Some aluminum hydroxide, may remain suspended in the water. The quantity in the water is dependent on the alum to fiber ratio. The neutralized slurry is then ready for the addition of the synthetic rubber binder.
These binders are those normally contemplated for use in the beater saturation processes. Typical of these synthetic rubbers are the butadiene-styrene copolymers (SBR) often containing 30-80% by weight butadiene. High styrene butadiene-styrene copolymers may also be used, although the tackiness characteristic of the lower styrene content is preferred in the binder solids. There may also be used the butadiene-acrylonitrile copolymers normally containing 50%80% by weight butadiene, the neoprenes (polychloroprenes), the homopolymers of butadiene as well as homopolyrners and/ or copolymers of butadiene homologs such as isoprene all can be used as binders in the present system; the so-called butyl rubber latices are useful.
The synthetic rubber latex will simply be added to the neutralized slurry in the requisite amount. In order to form the textile substitute of the present invention, relatively huge amounts of rubber binder are necessary, based on the dry weight of the papermaking fibers. Therefore, an amount of synthetic rubber latex binder will be added to achieve a dry rubber solids content of 200%650% by weight based on the dry weight of the papermaking fibers. Such a large amount of rubber solids has normally been avoided in the beater saturation arts in the past since it is almost unavoidable to precipitate some of the rubber solids in the water rather than on the fibers. In the present process, however, it is acceptable and even desirable when some of the rubber content of the latex precipitates on the aluminum hydroxide in the water as opposed to precipitating on the fibers themselves. It is one of the advantages of the present invention that such precipitation of rubber solids in the water actually enhances the final product. Accordingly, a notorious disadvantage is turned to an advantage in the present process. The mere addition with agitation of the synthetic rubber latex to the neutralized slurry will bring about precipitation of all the rubber solids in the latex. This precipitation normally occurs fairly rapidly and in any case will be completed within half an hour, and in most cases within 15 minutes or less.
Once the rubber has been precipitated, the slurry is in condition to receive the staple synthetic fibers or other fibers and the water-soluble metal salt. The uncoated fibers will normally have a length in the range of inch to 1 inch and are added to the slurry of rubber-coated papermaking fibers in an amount of 50%900% by weight based on the dry weight of the papermaking fibers themselves. The usual agitation sufiices to distribute the staple fibers throughout the slurry. These staple fibers may be synthetic fibers such as rayon, acetate, polyamide fibers, polyester fibers, poly(vinyl chloride) fibers, and other hard-to-handle fibers as far as beater saturation is concerned.
After the staple fibers have been thoroughly distributed throughout the slurry, the water-soluble salt will then be added, if it has not been added prior to the addition of the staple fibers. It makes little difference in the process if the uncoated fiber or the water-soluble salt is first added to the slurry of coated fibers. These Water-soluble salts are those which result from the reaction of acetic acid or the inorganic mineral acids with the proper metallic compound. The inorganic mineral acids are typically hydrochloric acid, nitric acid, and sulfuric acid. The metallic portionthe cationof the water-soluble salt to be added to the slurry will be any of the metals found in the groups of the Periodic system mentioned earlier. Aluminum and chromium do not work in the control of processing characteristics of the slurry, probably because of the ease with which these two metals form anions with oxygen at an alkaline pH. The metals which function in the present method appear to do so by virtue of the nature of their behavior after the salt-containing slurry has been made alkaline, to be described below. Typical of the water-soluble salts Which operate in the present method are lead acetate, manganous chloride, ferrous chloride, ferric chloride, calcium chloride, cobalt chloride, nickel chloride, and the corresponding nitrates and water-soluble sulfates thereof. There should also be mentioned magnesium sulfate, copper sulfate, zinc nitrate, cadmium sulfate, and beryllium sulfate, and the corresponding watersoluble chlorides thereof.
The Water-soluble salts are preferably added in the form of their water solution, with agitation. The maximum amount of the salt to be added to control the drainage characteristics is determined by the weight of the cation portion of the salt. The weight of the cation portion of the salt should not exceed about 50% of weight of the uncoated fibers on a dry basis. Larger amounts of the salt are not only wasteful, but may impart a harshness of hand to the finished sheet. As to the minimum amount of salt to be added, quite small amounts are effective. Activity of the different operable water-soluble salts will differ, but a reasonable minimum may be established at about 0.1% by weight of the cation portion of the salt based on the weight of the uncoated fibers.
For ease of distribution of the solution of the watersoluble salt and water throughout the slurry containing the precipitated rubber, it is preferred to use a dilute solution on the order of 1%5% by Weight of the salt in water. This solution will be added with agitation in order to distribute the water-soluble salt thoroughly throughout the slurry.
After the water-soluble salt has been thoroughly distributed throughout the slurry of coated fibers, and after the uncoated fibers have been added, it is necessary to add sufficient caustic to adjust the pH of the slurry to a range 8.5-11.5 and preferably to 9.5. Although ammonium hydroxide, sodium hydroxide, or potassium hydroxide may be used, ammonium hydroxide may form soluble complexes with some of the metals used in making the water-soluble metal salt. Potassium hydroxide is comparatively expensive. For these reasons, sodium hy- Weight and Type of Papermoking Fiber Weight and Type of Staple Fiber in redients will be known and occasional checks may be all that is required.
The final slurry, with its pH of about 9.5, is ready for dewatering as soon as the caustic has been thoroughly admixed. A product will be formed from the resulting slurry by removing water therefrom as by introducing the agitated slurry onto a papermaking or feltmaking wire or cylinder. The drainage characteristics of the particular finished slurry will be found to be controllable by the amount of water-soluble metal salt that has been added within the limits described above. Increased amounts of the water-soluble salt increase the drainage time and decrease the Canadian 3-gram freeness. In accordance with the present method then, it is possible to decide exactly the drainage characteristics desired of the slurry under preparation, and adjust the water-soluble metal salt addition accordingly.
The slurry will then be formed into a sheet in a papermaking wire or cylinder, or other device. On drying, it will be found that the sheet has an extraordinary drape for a heater saturated, water-laid product, reminiscent of a textile. The hand is soft and there is little or none of the harshness or brittleness normally associated with a paper or felt product. The product does not crease in the normal sense of the word and, in some modifications, is surprisingly difiicult to tear with the fingers in thicknesses of about 0.02 inch. Hence this product may be used in place of woven cloth and has many applications such as doilies, tablecloths, and certain items of clothing.
The following examples illustrate several embodiments of the invention. All parts are by weight unless otherwise stated.
Example 1 A series of runs was made in which one part by weight of a papermaking fiber was dispersed in 1,850 parts water, and the slurry was refined. There was then added 15 parts by volume of a 20% by weight aluminum sulfate solution with agitation. Sufiicient 10% sodium hydroxide solution was then added in each case to obtain a pH of 7.0. A synthetic rubber latex was then added with agitation. Following precipitation of the latex there was then added 8 parts by volume of a 1.2% by weight magnesium sulfate solution, followed by the addition of uncoated staple fiber, followed by the addition of sufficient 10% by weight sodium hydroxide solution to achieve a pH of 9.5. The following table illustrates the particular ingredients in the amounts used.
Weight and Type of Binder 1, leather 1, asbestos 4 olyamide (nylon 3 4 inch) 6: poly amide (nylon: inch) 3, but-adlene-styrene copolyme. 5, butadiene-styrene copolyrnr. 3, butyl rubber. or
2, butadiene-styrene.
droxide is the caustic of choice. Preferably the caustic will be added in the form of its water solution, the concentration being any convenient concentration, a 10% solution of the caustic being a good average. Sufficient of the caustic solution is added with agitation to establish a pH within the above-mentioned pH range in the slurry, the target pH being 9.5. A pH higher than about 11.5 may unduly harm or react with the ingredients in the slurry, while a pH below about 8.5 is not high enough to achieve the full desirable effects of the present method. The pH of the resultant slurry may be checked in known manner with a suitable pH meter or test paper. Once the process has become stabilized in the commercial pro- 6, regenerated cellulose (rayon, inch) lIi-iageneratedbellirlose (rayon, inch)" 12, polyester (Dacron, inch) 9, acrylio/(Qrlon, M inch) 6, glass, 4 men 6, cellulose acetate, M inch 6, cotton lint-ers 3, butadicne-styrene.
3, neoprene.
o. 3, butadiene-styrene copoly Do. mer.
Each of the finished slurries described above was formed into a sheet measuring 0.020 inch thickness, dried at 220 F., and cooled. Each sheet was soft and flexible and possessed none of the harshness and brittleness of normal paper and felt products. Each sheet had the hand and drape of a textile product. The second sheet in the above table, the one made with 1 part asbestos, 6 parts nylon, and 5 parts binder, was exceedingly strong and difiicult to tear with fingers.
Example 2 Runs were made using 2 parts asbestos fibers in 1,850 parts water, followed by the usual alum-sodium hydroxduction of any particular product, the amounts of the ide treatment, followed by addition of 6 parts (dry basis) butadiene-styrene copolymer binder. The precipitated slurry before treatment was unsuitable for forming a sheet product due to the large amount of precipitated fines which were lost with the white water. The addition of caustic alone to a pH of 9.5 caused the formation of large clumps, again unsuitable for sheet formation. However, the addition of a 1% solution of the metal salt indicated in the amount indicated improved the sheet formation as opposed to either the untreated slurry, or the caustic treated slurry in the absence of the metal salt. The following table identifies the metal salt and the volume of 1% by weight solution used.
The large amount of calcium chloride and barium chloride is apparently needed due to the presence of sulfate ion in the slurry.
We claim:
1. The method of forming a heater saturated, nonwoven textile substitute which comprises forming in water a slurry of papermaking fibers, adding alum to said slurry, adjusting the pH of the alum-treated slurry to a range of 6-8 by adding alkali thereto, adding a synthetic rubber latex in an amount of 200%650% by Weight dry rubber solids based on the dry weight of the papermaking fibers to the neutralized slurry whereby the solids content of the binder precipitates, adding to the resulting slurry in indifferent order long, staple fibers in an amount of %900% by weight based on the dry weight of the papermaking fibers and a water-soluble salt of a metal selected from the group consisting of metals in Groups I, II, IV, VII, and VIII of the Periodic Table, adding sufficient alkali to the salt-treated slurry containing said staple fibers to achieve a pH in the range of 8.511.5 to form an insoluble hydroxide with the metal ion from the salt, and forming a sheet from the resulting slurry.
2. The method according to claim 1 wherein said alkali comprises sodium hydroxide.
3. The method according to claim 1 wherein said water-soluble salt comprises magnesium sulfate.
4. The method according to claim 1 wherein the pH adjustment of the alum-treated slurry is about 7 and the pH of the salt-treated slurry is about 9.5.
5. The method according to claim 1 wherein said synthetic rubber binder is added in an amount of about 500% by Weight based on the dry Weight of the papermaking fibers.
6. The method according to claim 1 wherein said staple fibers are added in an amount of about 400% by weight based on the dry weight of the papermaking fibers.
7. The method according to claim 1 wherein said papermaking fibers comprise asbestos fibers.
8. The method according to claim 1 wherein said staple fibers comp-rise nylon fibers.
9. A product made according to the method of claim 1.
References Cited UNITED STATES PATENTS S. LEON BASHORE, Primary Examiner.

Claims (1)

1. THE METHOD OF FORMING A BEATER SATURATED, NONWOVEN TEXTILE SUBSTITUTE WHICH COMPRISES FORMING IN WATER A SLURRY OF PAPERMAKING FIBERS, ADDING ALUM TO SAID SLURRY, ADJUSTING THE PH OF THE ALUM-TREATED SLURRY TO A RANGE OF 6-8 BY ADDING ALKALI THERETO, ADDING A SYNTHETIC RUBBER LATEX IN AN AMOUNT OF 200%-650% BY WEIGHT DRY RUBBER SOLIDS BASED ON THE DRY WEIGHT OF THE PAPERMAKING FIBERS TO THE NEUTRALIZED SLURRY WHEREBY THE SOLIDS CONTENT OF THE BINDER PRECIPITATES, ADDING TO THE RESULINGT SLURRY IN INDIFFERENT ORDER LONG, STAPLE FIBERS IN AN AMOUNT OF 50%-900% BY WEIGHT BASED ON THE DRY WEIGHT OF THE PAPERMAKING FIBERS AND A WATER-SOLUBLE SALT OF A METAL SELECTED FROM THE GROUP CONSISTING OF METALS IN GROUPS I, II, IV, VII, AND VIII OF THE PERIODIC TABLE, ADDING SUFFICIENT ALKALI TO THE SALT-TREATED SLURRY CONTAINING SAID STAPLE FIBERS TO ACHIEVE A PH IN THE RANGE OF 8.5-11.5 TO FORM AN INSOLUBLE HYDROXIDE WITH THE METAL ION FROM THE SALT, AND FORMING A SHEET FROM THE RESULTING SLURRY.
US442481A 1965-03-24 1965-03-24 Method of making beater-saturated water-laid product containing paper-making and textile staple fibers Expired - Lifetime US3344016A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US442481A US3344016A (en) 1965-03-24 1965-03-24 Method of making beater-saturated water-laid product containing paper-making and textile staple fibers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US442481A US3344016A (en) 1965-03-24 1965-03-24 Method of making beater-saturated water-laid product containing paper-making and textile staple fibers

Publications (1)

Publication Number Publication Date
US3344016A true US3344016A (en) 1967-09-26

Family

ID=23756951

Family Applications (1)

Application Number Title Priority Date Filing Date
US442481A Expired - Lifetime US3344016A (en) 1965-03-24 1965-03-24 Method of making beater-saturated water-laid product containing paper-making and textile staple fibers

Country Status (1)

Country Link
US (1) US3344016A (en)

Cited By (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2215993A1 (en) * 1973-02-01 1974-08-30 Ghh Basel Ag Fibrous filter pad impregnated with metal salt - provides inexpensive water purification for small communities and single households
US3870596A (en) * 1971-06-22 1975-03-11 Tachikawa Res Inst Process for the preparation of dispersion water for incompletely regenerated cellulose substance
US3965020A (en) * 1973-09-20 1976-06-22 Johns-Manville Corporation Siliceous thermal insulation and method of making same
US4247364A (en) * 1979-07-02 1981-01-27 Armstrong Cork Company Method of making a smooth, dimensionally stable, mica-filled, glass fiber sheet
FR2550244A1 (en) * 1983-08-01 1985-02-08 Armstrong World Ind Inc PROCESS FOR FORMING A SATURATION-PRECIPITATION COATED SHEET USING CARBONATE IONS
US4853083A (en) * 1983-08-01 1989-08-01 Armstrong World Industries, Inc. Method of forming beater-saturated sheet using carbonate ion
EP0723047A2 (en) * 1995-01-13 1996-07-24 Hercules Incorporated Improving the strength of paper made from pulp containing surface active carboxyl compounds
US20210381166A1 (en) * 2020-06-09 2021-12-09 Evrnu, Spc Processing cellulose-containing materials for paper or packaging materials
US11230811B2 (en) 2018-08-23 2022-01-25 Eastman Chemical Company Recycle bale comprising cellulose ester
US11286619B2 (en) 2018-08-23 2022-03-29 Eastman Chemical Company Bale of virgin cellulose and cellulose ester
US11299854B2 (en) 2018-08-23 2022-04-12 Eastman Chemical Company Paper product articles
US11306433B2 (en) 2018-08-23 2022-04-19 Eastman Chemical Company Composition of matter effluent from refiner of a wet laid process
US11313081B2 (en) 2018-08-23 2022-04-26 Eastman Chemical Company Beverage filtration article
US11332885B2 (en) 2018-08-23 2022-05-17 Eastman Chemical Company Water removal between wire and wet press of a paper mill process
US11332888B2 (en) 2018-08-23 2022-05-17 Eastman Chemical Company Paper composition cellulose and cellulose ester for improved texturing
US11339537B2 (en) 2018-08-23 2022-05-24 Eastman Chemical Company Paper bag
US11390996B2 (en) 2018-08-23 2022-07-19 Eastman Chemical Company Elongated tubular articles from wet-laid webs
US11390991B2 (en) 2018-08-23 2022-07-19 Eastman Chemical Company Addition of cellulose esters to a paper mill without substantial modifications
US11396726B2 (en) 2018-08-23 2022-07-26 Eastman Chemical Company Air filtration articles
US11401660B2 (en) 2018-08-23 2022-08-02 Eastman Chemical Company Broke composition of matter
US11401659B2 (en) 2018-08-23 2022-08-02 Eastman Chemical Company Process to produce a paper article comprising cellulose fibers and a staple fiber
US11408128B2 (en) 2018-08-23 2022-08-09 Eastman Chemical Company Sheet with high sizing acceptance
US11414818B2 (en) 2018-08-23 2022-08-16 Eastman Chemical Company Dewatering in paper making process
US11414791B2 (en) 2018-08-23 2022-08-16 Eastman Chemical Company Recycled deinked sheet articles
US11421387B2 (en) 2018-08-23 2022-08-23 Eastman Chemical Company Tissue product comprising cellulose acetate
US11420784B2 (en) 2018-08-23 2022-08-23 Eastman Chemical Company Food packaging articles
US11421385B2 (en) 2018-08-23 2022-08-23 Eastman Chemical Company Soft wipe comprising cellulose acetate
US11441267B2 (en) 2018-08-23 2022-09-13 Eastman Chemical Company Refining to a desirable freeness
US11466408B2 (en) 2018-08-23 2022-10-11 Eastman Chemical Company Highly absorbent articles
US11479919B2 (en) 2018-08-23 2022-10-25 Eastman Chemical Company Molded articles from a fiber slurry
US11492757B2 (en) 2018-08-23 2022-11-08 Eastman Chemical Company Composition of matter in a post-refiner blend zone
US11492756B2 (en) 2018-08-23 2022-11-08 Eastman Chemical Company Paper press process with high hydrolic pressure
US11492755B2 (en) 2018-08-23 2022-11-08 Eastman Chemical Company Waste recycle composition
US11512433B2 (en) 2018-08-23 2022-11-29 Eastman Chemical Company Composition of matter feed to a head box
US11519132B2 (en) 2018-08-23 2022-12-06 Eastman Chemical Company Composition of matter in stock preparation zone of wet laid process
US11525215B2 (en) 2018-08-23 2022-12-13 Eastman Chemical Company Cellulose and cellulose ester film
US11530516B2 (en) 2018-08-23 2022-12-20 Eastman Chemical Company Composition of matter in a pre-refiner blend zone
US11639579B2 (en) 2018-08-23 2023-05-02 Eastman Chemical Company Recycle pulp comprising cellulose acetate

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2375245A (en) * 1941-08-25 1945-05-08 Paul W Pretzel Manufacture of rubberized fibers and sheets
US3057772A (en) * 1957-04-23 1962-10-09 Riegel Paper Corp Synthetic fiber paper and method of making same

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2375245A (en) * 1941-08-25 1945-05-08 Paul W Pretzel Manufacture of rubberized fibers and sheets
US3057772A (en) * 1957-04-23 1962-10-09 Riegel Paper Corp Synthetic fiber paper and method of making same

Cited By (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3870596A (en) * 1971-06-22 1975-03-11 Tachikawa Res Inst Process for the preparation of dispersion water for incompletely regenerated cellulose substance
FR2215993A1 (en) * 1973-02-01 1974-08-30 Ghh Basel Ag Fibrous filter pad impregnated with metal salt - provides inexpensive water purification for small communities and single households
US3965020A (en) * 1973-09-20 1976-06-22 Johns-Manville Corporation Siliceous thermal insulation and method of making same
US4247364A (en) * 1979-07-02 1981-01-27 Armstrong Cork Company Method of making a smooth, dimensionally stable, mica-filled, glass fiber sheet
FR2550244A1 (en) * 1983-08-01 1985-02-08 Armstrong World Ind Inc PROCESS FOR FORMING A SATURATION-PRECIPITATION COATED SHEET USING CARBONATE IONS
US4853083A (en) * 1983-08-01 1989-08-01 Armstrong World Industries, Inc. Method of forming beater-saturated sheet using carbonate ion
EP0723047A2 (en) * 1995-01-13 1996-07-24 Hercules Incorporated Improving the strength of paper made from pulp containing surface active carboxyl compounds
EP0723047A3 (en) * 1995-01-13 1997-09-24 Hercules Inc Improving the strength of paper made from pulp containing surface active carboxyl compounds
US6228217B1 (en) 1995-01-13 2001-05-08 Hercules Incorporated Strength of paper made from pulp containing surface active, carboxyl compounds
US11396726B2 (en) 2018-08-23 2022-07-26 Eastman Chemical Company Air filtration articles
US11414818B2 (en) 2018-08-23 2022-08-16 Eastman Chemical Company Dewatering in paper making process
US11286619B2 (en) 2018-08-23 2022-03-29 Eastman Chemical Company Bale of virgin cellulose and cellulose ester
US11299854B2 (en) 2018-08-23 2022-04-12 Eastman Chemical Company Paper product articles
US11306433B2 (en) 2018-08-23 2022-04-19 Eastman Chemical Company Composition of matter effluent from refiner of a wet laid process
US11313081B2 (en) 2018-08-23 2022-04-26 Eastman Chemical Company Beverage filtration article
US11332885B2 (en) 2018-08-23 2022-05-17 Eastman Chemical Company Water removal between wire and wet press of a paper mill process
US11332888B2 (en) 2018-08-23 2022-05-17 Eastman Chemical Company Paper composition cellulose and cellulose ester for improved texturing
US11339537B2 (en) 2018-08-23 2022-05-24 Eastman Chemical Company Paper bag
US11390996B2 (en) 2018-08-23 2022-07-19 Eastman Chemical Company Elongated tubular articles from wet-laid webs
US11390991B2 (en) 2018-08-23 2022-07-19 Eastman Chemical Company Addition of cellulose esters to a paper mill without substantial modifications
US11639579B2 (en) 2018-08-23 2023-05-02 Eastman Chemical Company Recycle pulp comprising cellulose acetate
US11401660B2 (en) 2018-08-23 2022-08-02 Eastman Chemical Company Broke composition of matter
US11401659B2 (en) 2018-08-23 2022-08-02 Eastman Chemical Company Process to produce a paper article comprising cellulose fibers and a staple fiber
US11408128B2 (en) 2018-08-23 2022-08-09 Eastman Chemical Company Sheet with high sizing acceptance
US11230811B2 (en) 2018-08-23 2022-01-25 Eastman Chemical Company Recycle bale comprising cellulose ester
US11414791B2 (en) 2018-08-23 2022-08-16 Eastman Chemical Company Recycled deinked sheet articles
US11421387B2 (en) 2018-08-23 2022-08-23 Eastman Chemical Company Tissue product comprising cellulose acetate
US11420784B2 (en) 2018-08-23 2022-08-23 Eastman Chemical Company Food packaging articles
US11421385B2 (en) 2018-08-23 2022-08-23 Eastman Chemical Company Soft wipe comprising cellulose acetate
US11441267B2 (en) 2018-08-23 2022-09-13 Eastman Chemical Company Refining to a desirable freeness
US11466408B2 (en) 2018-08-23 2022-10-11 Eastman Chemical Company Highly absorbent articles
US11479919B2 (en) 2018-08-23 2022-10-25 Eastman Chemical Company Molded articles from a fiber slurry
US11492757B2 (en) 2018-08-23 2022-11-08 Eastman Chemical Company Composition of matter in a post-refiner blend zone
US11492756B2 (en) 2018-08-23 2022-11-08 Eastman Chemical Company Paper press process with high hydrolic pressure
US11492755B2 (en) 2018-08-23 2022-11-08 Eastman Chemical Company Waste recycle composition
US11512433B2 (en) 2018-08-23 2022-11-29 Eastman Chemical Company Composition of matter feed to a head box
US11519132B2 (en) 2018-08-23 2022-12-06 Eastman Chemical Company Composition of matter in stock preparation zone of wet laid process
US11525215B2 (en) 2018-08-23 2022-12-13 Eastman Chemical Company Cellulose and cellulose ester film
US11530516B2 (en) 2018-08-23 2022-12-20 Eastman Chemical Company Composition of matter in a pre-refiner blend zone
US20210381166A1 (en) * 2020-06-09 2021-12-09 Evrnu, Spc Processing cellulose-containing materials for paper or packaging materials

Similar Documents

Publication Publication Date Title
US3344016A (en) Method of making beater-saturated water-laid product containing paper-making and textile staple fibers
US3184373A (en) Filled paper containing a mixture of resin and mucilaginous material as a retention aid and process for producing said paper
US2810644A (en) Paper products and method of making the same
US2658828A (en) Process of combining synthetic resins and other materials with cellulose
US2582840A (en) Sizing fibrous materials with modified urea-formaldehyde resin
US3193446A (en) Latex bonded asbestos fiber sheet material
US3081219A (en) Prevention of deposition of pitch in papermaking
US2999038A (en) Method of producing wet-strength papers
US2599092A (en) Multiple layer paper containing pigmented pulp and method of making
US3139373A (en) Process for the internal sizing of paper with a salt of a substituted succinic acid
US2668111A (en) Paper making processes
US2599091A (en) Forming pigment in cellulose fiber and paper containing the pigmented fiber
US2549177A (en) Sized paper, composition therefor, and method of making same
US2890978A (en) Paper of high dry strength and low wet strength
US3344017A (en) Method of controlling drainage time of beater saturated slurries
US2192488A (en) Method of making paper
US3223580A (en) Dimensionally stable mineral wool fiberboard
US3151017A (en) Selected treatment of fiber blends with resins
US1998758A (en) Treatment of paper pulp
US2738791A (en) Cigarette paper
US3008868A (en) Drainage rate of cellulosic papermaking slurries
US3062703A (en) Wet-strength paper containing polymeric dialdehydes
US2635972A (en) Coated paper and process for making same
US3019157A (en) Web-forming fibrous suspensions of improved freeness
US2971879A (en) Water-laid fibrous sheets