Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – At least one aryl ring which is part of a fused or bridged...
Reexamination Certificate
1999-02-09
2001-09-11
Reddick, Judy M. (Department: 1713)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
At least one aryl ring which is part of a fused or bridged...
C524S379000, C524S389000, C524S492000, C524S512000, C524S565000, C524S566000, C525S328700, C525S329100, C525S342000, C525S383000, C523S204000, C523S208000, C523S209000
Reexamination Certificate
active
06288158
ABSTRACT:
The present invention relates to superabsorbing polymers based on finely divided crosslinked or uncrosslinked polyacrylonitrile emulsions and to the improved applicational characteristics thereof.
Superabsorbing polymers are known and are primarily used in the production of diapers and incontinence articles, but are also used as water storage materials in agriculture and for sheathing electrical cables. Commercially available superabsorbing polymers are generally loosely crosslinked, water-insoluble polymers based on alkali metal salts of polyacrylic acid or on copolymers of acrylic acid and acrylamide, which are obtained by free-radically initiated copolymerization of acrylic acid and polyfunctional monomers, such as for example divinylbenzene, ethylene glycol dimethacrylate, ethylene glycol diallyl ether, butanediol acrylate, hexanediol methacrylate, polyglycol diacrylate, trimethylolpropane diacrylate, allyl acrylate, diallyl acrylamide, triallylamine, diallyl ether, methylenebisacrylamide and N-methylolacrylamide. By virtue of their molecular structure, such polymers are capable of absorbing large quantities of liquids by swelling and forming hydrogels and also of retaining these liquids under pressure.
European patent application EP-A 0,670,335 discloses that products having excellent superabsorbent properties may be produced by partial alkaline hydrolysis of finely divided aqueous emulsions of linear homo- and/or copolymers of acrylonitrile, in which products 30 to 60 mol. % of the nitrile groups have been converted into carboxylate groups, 20 to 60 mol. % of the nitrile groups have been converted into carbonamide groups and 10 to 20 mol. % of the nitrile groups remain unchanged. These uncrosslinked superabsorbing polymers exhibit an extraordinarily high swelling capacity of up to 1000 g/g in water and of up to 90 g/g in physiological sodium chloride solution. It is also known from EP-A 0,697,416 that superabsorbing polymers having excellent applicational characteristics may also be obtained by partial alkaline hydrolysis of finely divided aqueous emulsions of acrylonitrile homo- and/or copolymers weakly crosslinked by the incorporation of polyfunctional monomers. The superabsorbing polymers produced from crosslinked polyacrylonitrile emulsions, the nitrile groups of which have been converted to an extent of 30 to 80 mol. % into carboxylate groups, to an extent of 20 to 70 mol. % into carbonamide groups, and which polymers still contain between 0 and 20 mol. % of unchanged nitrile groups, are capable of absorbing up to 700 g/g of water and up to 60 g/g of physiological sodium chloride solution.
The finely divided, aqueous, uncrosslinked or crosslinked polyacrylonitrile emulsions required for the production of the superabsorbing polymers are obtained by homo- and/or copolymerizing acrylonitrile in the presence of special anionic polymeric emulsifiers (DE-OS 4,233,026). The molecular weights of the uncrosslinked polyacrylonitrile emulsions produced using this process are within the range from 5×10
5
to 1×10
7
g/mol., preferably from 2×10
6
to 5×10
6
g/mol. The particle sizes of the uncrosslinked or crosslinked aqueous polyacrylonitrile emulsions are within the range between 100 and 300 nm, preferably between 100 and 200 nm (determined by laser correlation spectroscopy).
However, the superabsorbing polymers obtainable by partial alkaline hydrolysis of uncrosslinked or crosslinked aqueous polyacrylonitrile emulsions also exhibit some disadvantageous characteristics, among which a certain tendency towards “gel blocking” may in particular be mentioned. When these products are used in personal hygiene articles, such as for example diapers “gel blocking” results in a low initial transport rate of the liquid to be absorbed, which results in overall relatively poor liquid transport proper-ties and to low “absorbency under load”, i.e. when exposed to elevated pressure of, for example, 0.7 psi, there is a perceptible decrease in the absorbency of the superabsorbent particles. Such a process ultimately also results in low “rewet” values of the nappies.
This “gel blocking” behavior is also known in superabsorbents based on polyacrylic acid. In order to avoid or overcome this characteristic, which has a negative impact on product performance, the superabsorbents may be treated, for example, with antiblocking agents, such as for example silica gel, cellulose fluff or other synthetic or natural hydrophilic fibers or also materials which have a greater surface area than the superabsorbents themselves (c.f. DE-OS 4,442,606), Another method for avoiding the “gel blocking” behavior of superabsorbents is surface crosslinking of the superabsorbent particles with various crosslinking agents having at least two functional groups. DE-OS 4,020,780 accordingly mentions various alkylene carbonates, such as 1,3-dioxolan-2-one or 4-methyl-1,3-dioxolan-2-one as effective crosslinking agents, while DE-OS, 4,442,605 mentions aldehydes or also difunctional isocyanates. A feature common to all the methods listed therein is that, after surface crosslinking, the superabsorbents modified in this manner must be subjected to heat treatment at temperatures of between 150 and 300° C. in order to ensure that “gel blocking” is effectively prevented.
The object underlying the present invention was to avoid “gel blocking” and thus, to achieve an increase in the initial transport rate, an improvement in “absorbency under load” and the transport rate under load. This aim has been achieved according to the invention by performing surface crosslinking with difunctional compounds and simultaneously immobilizing silica in the surface structure of the superabsorbing polymers.
It has surprisingly been found that simultaneous crosslinking and immobilization of silica brings about a synergistic effect. This is manifested by a disappearance of “gel blocking” with a simultaneous increase in the initial transport rate and a distinct improvement in “absorbency under load” values at 0.3 and 0.7 psi.
Surface modification, which may also be described as immobilization, is performed on the already formed superabsorbent particles in a water/alcohol mixture with a water concentration of 2 to 15 wt. %, preferably of 6 to 12 wt. %, using formaldehyde or other aldehydes, for example glutaraldehyde, as crosslinking agents in the presence of silica. The already formed superabsorbent particles, used as starting materials are prepared by polymerizing a latex emulsion (in water), precipitating the polymer particles, drying them, grinding and sieving the product obtained as described in U.S. Pat. Nos. 5,496,890 and 5,635,569 incorporated herein by reference. Such particles, while superabsorbent, still show gel-blocking. In the inventive process, the surface of these particles is modified in an aqueous alcoholic medium by reaction with silica and an aldehyde (which acts as a crosslinking agent). The resulting modified particles show improved “absorbency under load” and a lesser degree of gel blocking. The silica suitable in the inventive process may be in solid or liquid form, preferably as colloidal silica in solution. Most preferably the silica is in the form of colloidal solution having a concentration of 15 to 30 wt. %, particle diameter of 5 to 50 nm, preferably 5 to 30 nm, specific surface of 1 00 to 450 m
2
/g and pH value of 4 to 6. The concentration of formaldehyde in the reaction mixture used to modify the superabsorbent is here 0.1 to 2.0 wt. %, preferably 0.3 to 1.0 wt. %, and the concentration of silica is between 0.3 and 2.0 wt. %, preferably 0.5 to 1.5 wt. % the percents being relative to the weight of the reaction mixture. Alcohols which may be used are methanol, ethanol, n-propanol, i-propanol or also mixtures of the stated alcohols, but preferably methanol or ethanol, at a liquid/solid ratio of 0.1 to 10, preferably of 0.2 to 1, and a solids content after filtration before drying of 50 to 90 wt. %, preferably of 70 to 85 wt. %. The drying temperature of the superabsorbing polymers treated with the ab
Korte Siegfried
Meyer Rolf-Volker
Sackmann Gunter
Schapowalov Sergej
Bayer Aktiengesellschaft
Gil Joseph C.
Preis Aron
Reddick Judy M.
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