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Porous, absorbent, polymeric macrostructures and methods of making the same    
United States Patent5102597   
Link to this pagehttp://www.wikipatents.com/5102597.html
Inventor(s)Roe; Donald C. (Cincinnati, OH); Lahrman; Frank H. (Cincinnati, OH); Berg; Charles J. (Cincinnati, OH)
AbstractAbsorbent polymeric macrostructures that are porous and comprise an interparticle crosslinked aggregate having a circumscribed dry volume greater than about 10.0 mm.sup.3. The interparticle crosslinked aggregate comprises a multiplicity of precursor particles of substantially water-insoluble, absorbent, hydrogel-forming, polymer material; and an interparticle crosslinking agent reacted with the polymer material of the precursor particles to form crosslink bonds between the precursor particles. Because of the particulate nature of the precursor particles, the macrostructure has pores between adjacent precursor particles. The pores are interconnected by intercommunicating channels such that the macrostructure is liquid permeable.
   














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Patent Text Patent PDF Print Page Summary File History
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Inventor     Roe; Donald C. (Cincinnati, OH); Lahrman; Frank H. (Cincinnati, OH); Berg; Charles J. (Cincinnati, OH)
Owner/Assignee     The Procter & Gamble Company (Cincinnati, OH)
Patent assignment
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Publication Date     April 7, 1992
Application Number     07/705,451
PAIR File History     Application Data   Transaction History
Image File Wrapper   Patent Term   Fees
Litigation
Filing Date     May 24, 1991
US Classification     264/126 521/84.1 521/88 521/94 521/95 521/142 521/149 521/919
Int'l Classification     B27J 005/00
Examiner     Foelak; Morton
Assistant Examiner    
Attorney/Law Firm     Miller; Steven W. Witte; Richard C. ,
Address
Parent Case     This is a division of application Ser. No. 503,393, filed on Apr. 2, 1990.
Priority Data    
USPTO Field of Search     264/126 521/84.1 521/88 521/94 521/95 521/142 521/149 521/919
Patent Tags     porous, absorbent, polymeric macrostructures methods making the
   
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 Technical Review Submit all comments and votes
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What is claimed is:

1. A method for producing a porous, absorbent, polymeric macrostructure comprising an interparticle crosslinked aggregate having pores interconnected by intercommunicating channels so that the macrostructure is liquid permeable, the method comprising the steps of:

(a) providing a multiplicity of precursor particles of substantially water-insoluble, absorbent, hydrogel-forming, polymer material;

(b) applying an interparticle crosslinking agent onto said precursor particles, said interparticle crosslinking agent being capable of reacting with said polymer material of said precursor particles;

(c) physically associating said precursor particles to form an aggregate having pores interconnected by intercommunicating channels; and

(d) reacting said interparticle crosslinking agent with said polymer material of said precursor particles of said aggregate, while maintaining the physical association of said precursor particles, to form crosslink bonds between said precursor particles to form an interparticle crosslinked aggregate macrostructure.

2. The method of claim 1 additionally comprising the step of surface crosslinking the macrostructure.

3. The method of claim 1 additionally comprising the step of shaping the aggregate to a desired shape, size, and/or density prior to step (d).

4. The method of claim 1 wherein step (d) comprises heating.

5. The method of claim 1 additionally comprising the step of adding reinforcing fibers to said precursor particles.

6. The method of claim 1 wherein said interparticle crosslinking agent comprises a monomer that is polymerized to form polymeric crosslink bonds between said precursor particles.

7. The method of claim 6 wherein step (d) comprises the step of initiating the polymerization reaction by irradiating said monomer.

8. The method of claim 1 wherein said precursor particles have a mass average particle size less than about 500 microns.

9. The method of claim 1 wherein said precursor particles have a mass average particle size less than about 300 microns.

10. The method of claim 1 wherein said precursor particles comprise fibers.

11. A method for producing a porous, absorbent, polymeric macrostructure comprising an interparticle crosslinked aggregate having pores interconnected by intercommunicating channels so that the macrostructure is liquid permeable, the method comprising the steps of:

(a) providing a multiplicity of substantially dry precursor particles of substantially water-insoluble, absorbent, hydrogel-forming, polymer material, said polymer material of said precursor particles being selected from the group consisting of hydrolyzed starch-acrylonitrile graft copolymer; partially neutralized starch-acrylonitrile graft copolymer; starch-acrylic acid graft copolymer; partially neutralized starch-acrylic acid graft copolymer; saponified vinyl acetate-acrylic ester copolymers; hydrolyzed acrylonitrile or acrylamide copolymers; slightly network crosslinked products of any of the foregoing copolymers; partially neutralized polyacrylic acid; or slightly network crosslinked products of partially neutralized polyacrylic acid;

(b) applying an interparticle crosslinking agent onto said precursor particles, said interparticle crosslinking agent being selected from the group consisting of polyhydric alcohol compounds, polyglycidyl ether compounds, polyfunctional aziridine compounds, polyfunctional amine compounds, and polyfunctional isocyanate compounds;

(c) physically associating said precursor particles to form an aggregate having pores interconnected by intercommunicating channels;

(d) shaping the aggregate to a desired shape, size, and/or density; and

(e) subsequently heating said interparticle crosslinking agent and said aggregate to react said interparticle crosslinking agent with said polymer material of said precursor particles of said aggregate, while maintaining the physical association of said precursor particles, to form crosslink bonds between said precursor particles to form an interparticle crosslinked aggregate macrostructure.

12. The method of claim 11 additionally comprising the step of adding fibers to said precursor particles prior to reacting said interparticle crosslinking agent with said polymer material of said precursor particles.

13. The method of claim 11 additionally comprising the step of surface crosslinking the macrostructure.

14. The method of claim 11 wherein said precursor particles comprise fibers.

15. The method of claim 11 wherein said interparticle crosslinking agent is mixed with water, an organic solvent, or mixtures thereof.

16. The method of claim 15 wherein step (d) comprises molding the aggregate.

17. The method of claim 15 wherein step (d) comprises forming the aggregate.

18. The method of claim 17 wherein step (d) comprises extruding said aggregate and subsequently rolling said aggregate to form a sheet.

19. The method of claim 11 wherein said interparticle crosslinking agent is selected from the group consisting of trimethylol propane, ethylene glycol, 1,2-propanediol, 1,3-propanediol, or glycerol; and said polymer material consists essentially of slightly network crosslinked products of partially neutralized polyacrylic acid.

20. The method of claim 19 wherein step (e) is carried out at a temperature in the range of from about 170.degree. C. to about 220.degree. C. for between about 3 hours and about 30 minutes.

21. The method of claim 20 wherein said interparticle crosslinking agent is mixed with water, an organic solvent, or mixtures thereof.

22. The method of claim 21 wherein step (d) comprises the steps of extruding the aggregate and then rolling said aggregate to form a sheet.

23. The method of claim 22 wherein step (b) comprises atomizing said interparticle crosslinking agent onto said precursor particles.

24. The method of claim 22 wherein the mass average particle size of said precursor particles is less than about 300 microns.

25. The method of claim 24 wherein at least about 95% by weight of said precursor particles have a particle size between about 150 microns and about 300 microns.

26. The method of claim 22 wherein the mass average particle size of said precursor particles is less than about 180 microns; and at least about 95% by weight of said precursor particles have a particle size between about 90 microns and about 180 microns.

27. The method of claim 19, 24, 25, or 26 additionally comprising the step of surface crosslinking said precursor particles of said macrostructure simultaneously with step (e).

28. The method of claim 14, 19, 21, or 24 additionally comprising the step of adding reinforcing fibers to said precursor particles prior to reacting said polymer material of said precursor particles with said interparticle crosslinking agent.
 Description Submit all comments and votes
 


FIELD OF THE INVENTION

The present invention relates to absorbent polymeric compositions which, upon contacting liquids such as water or body exudates, swell and imbibe such liquids. More specifically, the present invention relates to polymeric compositions that are macrostructures such as a sheet, film, or strip. Such absorbent polymeric macrostructures are porous so as to be liquid permeable. These porous, absorbent, polymeric macrostructures are useful by themselves or in absorbent articles such as diapers, adult incontinence pads, sanitary napkins, and the like. The present invention also relates to methods of producing such porous, absorbent, polymeric macrostructures.

BACKGROUND OF THE INVENTION

Particulate, absorbent, polymeric compositions are capable of absorbing large quantities of liquids such as water and body exudates and which are further capable of retaining such absorbed liquids under moderate pressures. These absorption characteristics of such polymeric compositions make them especially useful for incorporation into absorbent articles such as diapers. For example, U.S. Pat. No. 3,699,103 issued to Harper et al. on June 13, 1972 and U.S. Pat. 3,670,731 issued to Harmon on June 20, 1972, both disclose the use of particulate, absorbent, polymeric compositions (also referred to as hydrogels, superabsorbent, or hydrocolloid materials) in absorbent articles.

Conventional particulate, absorbent, polymeric compositions, however, have the limitation that the particles are not immobilized and are free to migrate during processing and/or use. Migration of the particles during processing can lead to material handling losses during manufacturing operations as well as nonhomogeneous incorporation of the particles into structures in which the particles are being used. A more significant problem, though, occurs when these particulate materials migrate during or after swelling. Such mobility leads to high resistance to liquid flow through the material due to the lack of stable interparticle capillary or liquid transport channels. This phenomenon is one form of what is commonly referred to as "gel blocking".

One attempt to overcome the performance limitations associated with particle mobility in the context of their use in absorbent articles has been the incorporation of the particulate, absorbent, polymeric compositions into tissue laminates (layered absorbent members). By encapsulating the particles between tissue layers, the overall particle mobility within an absorbent member is diminished. However, upon liquid contact, the particles within the laminate are often free to move relative to each other resulting in the breakdown of any preexistent interparticle capillary channels.

Another attempted solution has been to immobilize the particulate, absorbent, polymeric compositions by the addition of large quantities of liquid polyhydroxy compounds that act as an adhesive to hold the particles together or to a substrate. An example of this technology is disclosed in U.S. Pat. No. 4,410,571 issued to Korpman on Oct. 18, 1983. While this approach does limit migration before and, to some extent, during swelling, the particles eventually become detached from each other upon presentation of excess liquid to such polymeric compositions, resulting again in the breakdown of any preexisting capillary channels between the particles.

A further attempt to overcome the problem has been to produce a superabsorbent film via extrusion of a solution of a linear polymer and subsequent crosslinking of the polymer. An example of this technology is disclosed in U.S. Pat. No. 4,861,539 issued to Allen et al. on Aug. 29, 1989. While these superabsorbent films may absorb significant quantities of liquids, they have limited liquid transport properties and are prone to gel blocking due to their lack of internal capillary channels.

Therefore, the present invention seeks to resolve the above problems by providing a porous, absorbent, polymeric macrostructure.

Thus, it is an object of the present invention to provide absorbent polymeric macrostructures that are porous.

It is a further object of the present invention to provide absorbent polymeric macrostructures that remain intact and transport liquid even upon saturation with excess liquid.

It is a still further object of the present invention to provide absorbent polymeric macrostructures wherein the component precursor particles and pores retain their relative geometry and spatial relationships even upon saturation with excess liquid.

It is an even further object of the present invention to provide absorbent polymeric macrostructures that increase in liquid permeability upon swelling.

It is another object of the present invention to provide a method for producing such absorbent polymeric macrostructures.

It a further object of the present invention to provide improved absorbent products, absorbent members, and absorbent articles (such as diapers or sanitary napkins) incorporating the absorbent polymeric macrostructures of the present invention.

SUMMARY OF THE INVENTION

The present invention provides an absorbent polymeric macrostructure that is porous. The porous, absorbent, polymeric macrostructure comprises an interparticle crosslinked aggregate having a circumscribed dry volume greater than about 10.0 mm.sup.3. The interparticle crosslinked aggregate comprises a multiplicity of precursor particles of substantially water-insoluble, absorbent, hydrogel-forming, polymer material; and an interparticle crosslinking agent reacted with the polymer material of the precursor particles to form crosslink bonds between different precursor particles. Because of the particulate nature of the precursor particles, the macrostructure has pores between adjacent precursor particles. The pores are interconnected by intercommunicating channels such that the macrostructure is liquid permeable (i.e., has capillary transport channels).

Due to the interparticle crosslink bonds formed between the precursor particles forming the interparticle crosslinked aggregate, the resultant macrostructure has improved structural integrity, increased liquid acquisition and distribution rates, and minimal gel blocking characteristics. It has been found that when the macrostructure is contacted with liquids, the macrostructure swells generally isotropically even under moderate confining pressures, imbibes such liquids into the precursor particles, and absorbs such liquids into the pores. The isotropic swelling of the macrostructure allows the precursor particles and the pores to maintain their relative geometry and spatial relationships even when swollen. Thus, the macrostructures are relatively "fluid stable" in that the precursor particles do not dissociate from each other, thereby minimizing the incidence of gel blocking and allowing the capillary channels to be maintained and enlarged when swollen so that the macrostructure may acquire and transport subseque