Abstrict The invention provides a method of increasing the sorption capacity
of smectite clays which exhibit osmotic swelling such as montmorillonite
clays having predominately sodium as the exchangeable cation. The
invention further provides a clumping cat litter having excellent
cohesiveness comprising certain mixtures of a clay which exhibits
osmotic swelling, a cellulosic material, and optionally a density
controlling material, the clay, the cellulose material, and the
density controlling material having certain particle size distributions,
and the cat litter having a bulk density in the range from about
0.54 to about 0.96 g/cc and a sorption capacity greater than about
1.0 cc/g, wherein the concentration of the smectite clay is such
that upon wetting the litter the cohesiveness of the lump of wetted
litter is sufficient to allow its removal from a litter box, and
wherein the concentration of the smectite clay is insufficient to
prevent the lump of wetted litter from disintegrating in water over
time.
Claims What is claimed is:
1. A method of enhancing the sorption capacity of a smectite clay
which exhibits osmotic swelling and which has a particle size such
that at least about 95% of its particles pass through a 2000 micron
screen which comprises mixing with the smectite clay a particulate
cellulosic material having a particle size distribution such that
at least about 95% of its particles pass through a 2000 micron screen,
wherein the weight ratio of the cellulosic material to the smectite
clay is in the range from about 0.05 to about 3.0.
2. The method of claim 1 wherein the smectite clay has a particle
size distribution such that at least about 80% of its particles
are retained on a 297 micron screen and less than about 10% of its
particles pass through a 149 micron screen, and wherein the cellulosic
material has a particle size distribution such that at least about
65% of tis particles are retained on a 297 micron screen and less
than about 10% of its particles pass through a 149 micron screen.
3. The method of claim 1 or 2 wherein the cellulosic material is
selected from the group consisting of oat hulls, corn cobs, peanut
shells, citrus pulp, beet pulp, paper, cotton burrs, cottonseed
hulls, rice hulls, rice bran, peat and mixtures thereof.
4. A clumping litter box sorbent which when wetted with urine has
sufficient cohesiveness for removal of the lump of wetted litter
from a litter box which comprises from about 30% to about 80% of
a smectite clay which exhibits osmotic swelling and which has a
particle size distribution such that at least 95% of its particles
pass through a 2000 micron screen, at least about 80% of its particles
are retained on a 297 micron screen, and less than about 10% of
its particles pass through a 149 micron screen, from about 5% to
about 70% of a particulate cellulosic material having a particle
size distribution such that at least about 95% of its particles
pass through a 2000 micron screen, at least about 65% of its particles
are retained on a 297 micron screen, and less than about 10% of
its particles pass through a 149 micron screen, and from about 0%
to about 60% of a density control agent having a particle size distribution
such that at least about 95% of its particles pass through a 2000
micron screen, at least about 80% of its particles are retained
on a 250 micron screen, and less than about 10% of its particles
pass through a 149 micron screen, wherein the concentration of the
smectite clay, cellulosic material, and density control agent are
such that the sorbent has a bulk density in the range from about
0.54 to about 0.96 g/cc and an apparent sorption capacity greater
than about 1.0 cc/g, wherein the concentration of the smectite clay
is such that upon wetting the sorbent the cohesiveness of the lump
of wetted sorbent is sufficient to allow its removal from a litter
box, and wherein the concentration of the smectite clay is insufficient
to prevent the lump of wetted sorbent from disintegrating in water.
5. The sorbent of claim 4 wherein the cellulosic material is selected
from the group consisting of oat hulls, corn cobs, peanut shells,
citrus pulp, beet pulp, paper, cotton burrs, cottonseed hulls, rice
hulls, rice bran, peat, and mixtures thereof.
6. The sorbent of claim 4 or 5 wherein the density control agent
is an inorganic substance which does not exhibit osmotic swelling.
7. The sorbent of claim 4 or 5 wherein the density control agent
has a bulk density intermediate the bulk density of the smectite
clay and the cellulosic material.
8. The sorbent of claim 4 or 5 wherein the density control agent
is a clay which does not exhibit osmotic swelling.
9. The sorbent of claim 4 or 5 wherein the concentration the cellulosic
material is from about 5% to about 30%, and the concentration of
the density control agent is from 0% to about 50%.
10. In a method of cleaning an animal litter box and reducing litter
box odors wherein there is added to a litter box a clumping sorbent
which is capable of agglomerating upon contact with a liquid animal
dross to form an agglomerated mass of sufficient size and of sufficient
cohesive strength to allow physical removal of the agglomerated
mass from the litter box, the sorbent is contacted with the liquid
dross to form the agglomerated mass of the sorbent, and the agglomerated
mass is removed from the litter box, the improvement which comprises
utilizing as the clumping sorbent the sorbent of Claims 4 or 5.
11. The method of claim 10 wherein the density control agent is
an inorganic substance which does not exhibit osmotic swelling.
12. The method of claim 10 wherein the density control agent has
a bulk density between the bulk density of the smectite clay and
the cellulosic material.
13. The method of claim 10 wherein the density control agent is
a clay which does not exhibit osmotic swelling.
14. A method of preparing a clumping litter box sorbent which when
wetted with urine has sufficient cohesiveness for removal of the
lumps of wetted litter from a litter box containing the litter which
comprises mixing together from about 30% to about 80% by weight
of a smectite clay which exhibits osmotic swelling and which has
a particle size such that at least about 95% of the particles thereof
pass through a 2000 micron screen, from about 5% to about 70% by
weight of a cellulosic material having a particle size such that
at least about 95% of the particles thereof pass through a 2000
micron screen, from 0% to about 60% by weight of a density control
agent having a particle size such that at least 95% of the particles
thereof pass through a 2000 micron screen, and an aqueous liquid,
adjusting the mixture to the desired moisture content, and sieving
the mixture to obtain a sorbent which has a particle size distribution
such that at least about 95% of its particles pass through a 2000
micron screen, at least about 80% of its particles are retained
on a 297 micron screen, and less than about 10% of its particles
pass through a 149 micron screen, wherein the minimum concentration
of the smectite clay is such that upon wetting the sorbent the cohesiveness
of the lump of wetted sorbent is sufficient to allow its removal
from a litter box, wherein the maximum concentration of the smectite
clay is insufficient to prevent the lump of wetted sorbent from
disintegrating in water, and wherein the sorbent has a bulk density
in the range from about 0.54 g/cc to about 0.96 g/cc and an apparent
sorption capacity greater than about 1.0 cc/g.
15. The method of claim 14 wherein the smectite clay has a particle
size distribution such that at least about 80% of its particles
are retained on a 297 micron screen and less than about 10% of its
particles pass through a 149 micron screen, wherein the cellulosic
material has a particle size distribution such that at least about
65% of its particles are retained on a 297 micron screen and less
than about 10% of its particles pass through a 149 micron screen,
wherein the density control agent has a particle size distribution
such that at least about 65% of its particles are retained on a
297 micron screen and less than about 10% of its particles pass
through a 149 micron screen.
16. The method of claim 14 or 15 wherein the cellulosic material
is selected from the group consisting of oat hulls, corn cobs, peanut
shells, citrus pulp, beet pulp, paper, cotton burrs, cottonseed
hulls, rice hulls, rice bran, peat, and mixtures thereof, and wherein
the density control agent is an inorganic substance which does not
exhibit osmotic swelling.
Description FIELD OF THE INVENTION
The invention pertains to a method of deodorizing animal wastes,
and more particularly the excreta from pets, such as cats.
BACKGROUND OF THE INVENTION
Heretofore, many efforts have been made to develop an effective
and inexpensive litter for animals, especially household pets, particularly
cats. Thus it has been disclosed in various patents to use alone
or in various combinations urine sorptive materials, odor-inhibiting
or control chemicals or materials, antioxidants, microbial inhibitors,
surfactants, dyes, antistatic agents, flame retardants, binders,
encapsulants, neutralizing agents, weighting or density control
agents, and other materials. Representative of the many materials
disclosed to provide one or more of these characteristics are: siliceous
minerals such as natural or synthetic clays (bentonite, attapulgite,
fuller's earth, sepiolite, kaolin), diatomaceous earth, mica, talc,
sand, finely divided quartz, vermiculite, perlite, fly ash, pumice,
zeolite molecular sieves, opalite, bottom ash, boiler slag, synthetic
porous silicas and silicates, hydrophobic microporous crystalline
tectosilicates of regular geometry having aluminum-free sites in
a siliceous lattice, and the like; natural or agriculturally-grown
materials and by-products thereof, such as chlorophyll-containing
materials (alfalfa, algae, broome grass, timothy grass, metallic
chlorophyllin salts, stems and leaves of leaf meal such as ipilipil
niseacacia, etc.), peanut shells, cedar, wood shavings, sawdust,
wood flour, bagasse, corncobs, sugar beet pulp, citrus pulp, alphacellulose
fiber stock, sulphite cellulosic paper stock, waste paper, paper
sludge, hay, husks, bark, straw, gelatinizable carbohydrates, sunflower
hulls, partially pyrolyzed cellulosic materials, sagebrush, sorghum,
cotton seed hulls, popcorn, peat moss, tomato pumice, grain, potato,
cereal or grain hulls such as corn, rice, wheat, oats, and the like,
apple pulp and grape pulp; foamed plastics (polystyrene, polyurethanes,
phenolic resins, cellular cellulose acetate, etc.); porous plastic
beads; cloth; synthetic sorptive granules based on commercial grade
plaster (calcium sulfate dihydrate); wax or paraffin coated hydrophobic
substantially nonabsorbent and nonwater wettable granular material;
porous inorganic material which has been uniformly contacted with
a gaseous or liquid acidic substance to neutralize alkalinity therein
and provide a pH between 5.8 and 6.2; porous inorganic material
treated with a water-soluble zinc salt and having a pH from approximately
7 to 9; absorbent pads; calcium carbonate; Portland cement; activated
carbon; alumina; coal residues; recycled molasses serum; in-situ
polymerized monomer or monomers containing at least one acidic functional
group present in the molecule; water soluble or dispersible materials
having colloidal properties in water including silicates, preferably
alkali metal silicates, pyrophosphates, preferably alkali metal
pyrophosphates, polysaccharides, preferably cellulose derivatives,
alginates, or starch; polyvinylpyrrolidone; anhydrous sodium sulfate;
citric acid; sodium chloride; sodium or ammonium persulfate and
a buffering agent; water absorbent polymers; adhesive-type soluble
lignin pelletizing aid; cyclodextrin; thermoplastic polymers, crosslinkable
natural gums such as the polygalactomannan gums, xanthan gum, or
alginate; pheromone-like attractant substances; a veterinary composition
for preventing feline urological syndrome; Plaster of Paris, calcined
alkaline earth metal oxides; aluminum sulfate; carbonates, bicarbonates;
hydrogen phosphates; benzaldehyde green; rose bengal; certain quaternary
ammonium compounds; proprionates; N-alkylpyridinium proprionates;
halogenated aromatic hydrocarbons; undecylenic acid; aldehyde derivatives,
thiocyanates; carbamates; azo chlorides; modified phenols; oxyalkylated
alkylphenols; alkyl sulfate salts; alkylbenzene sulfonate salts;
oxyalkylated alcohols; water soluble or dispersible gums and polymers,
such as guar gum, micro-crystalline cellulose, pregelatinized starches,
methacrylic and acrylic polymers and copolymers, cellulose derivatives
(carboxymethyl cellulose, hydroxyethyl cellulose, methyl cellulose),
polyvinyl alcohol, polyethylene oxides, carbohydrates, and proteins;
camphane derivatives; various aromatic oils such as pine oil, citrus
oils; oil of cloves, and cinnamon oil; menthol; camphor; sodium
dihydrogen phosphate; potassium dihydrogen phosphate; potassium
acid phthalate; cherry pit extract; certain hydroxyamic acids and
salts thereof; perfumes; fragrances; vitamin E; chlorine dioxide;
sodium bicarbonate; gypsum; sagebrush oil; microencapsulated fragrance
or deodorizer; salts of transition metals of Group Ib or Group IIb
of the periodic table of the elements; ferrous sulphate hyptahydrate;
borax; and p-hydroxybenzoate.
In the last 10 years or so there has developed a new type of cat
litter which "captures" the urine in a "ball"
or "clump" of litter which can be scooped from the nonwetted
litter for easy removal. See for example the following U.S. patents,
incorporated herein by reference: 4685420 (Stuart); 5000115
(Hughes). These so-called "clumping" litters have been
based on one or more clays generally having a particle size within
the range from about 297 microns to about 2000 microns. Although
these clumping litters have been a vast improvement in eliminating
the waste before it generates obnoxious odors, these clumping litters
still possess one or more undesirable properties or characteristics.
These include: high bulk density; poor clumping (poor cohesiveness
of the wetted litter); poor urine sorption capacity; excessive wicking
or sorption or the urine into the bulk of the litter before the
wetted ball of litter is removed.
Thus there is still a need for a superior litter which eliminates
or reduces the odors associated with animal urine.
I have now discovered that the sorption capacity of clays which
exhibit osmotic swelling can be dramatically increased by admixing
therewith a particulate cellulosic material. The sorption capacity
of the admixture is synergistically increased as compared to the
calculated sorption capacity of the clay and the cellulosic material
at their respective concentrations. Furthermore the bulk density
of the admixtures are synergistically decreased as compared to the
calculated bulk density of the clay and the cellulosic material
at their respective concentrations.
Thus it is an object of this invention to provide a method of increasing
the sorption capacity of clays which exhibit osmotic swelling.
Another object of this invention is to provide a clumping sorbent
having superior sorption capacity and sufficient cohesiveness when
wetted with an aqueous liquid, such as urine, to be easily separated
from the nonwetted sorbent particles.
Another object of this invention is to provide a clumping cat litter
having a bulk density from about 0.54 to about 0.96 g/cc and a sorption
capacity greater than 1.0 cc/g, the litter containing sufficient
clay which exhibits osmotic swelling to provide sufficient cohesiveness
for easy removal of wetted litter from a litter box, and insufficient
of such clay to prevent the disintegration of the litter upon aging
in water.
These and other objects of the invention will be readily apparent
to one skilled in the art as the description thereof proceeds.
While the invention is susceptible of various modifications and
alternative forms, specific embodiments thereof will hereinafter
be described in detail and shown by way of example. It should be
understood, however, that it is not intended to limit the invention
to the particular forms disclosed, but, on the contrary, the invention
is to cover all modifications and alternatives falling within the
spirit and scope of the invention as expressed in the appended claims.
The compositions can comprise, consist essentially of, or consist
of the stated materials. The method can comprise, consist essentially
of, or consist of the stated steps with the stated materials.
DESCRIPTION OF THE PREFERRED EMBODIMENTS OF THE INVENTION
The clays which are useful in the methods and sorbents of this
invention are smectite-type clays which have a cation exchange capacity
of at least 50 milliequivalents per 100 grams of clay which have
sufficient of the exchangeable cations being selected from the group
consisting of sodium, lithium, and mixtures thereof, such that the
clay exhibits osmotic swelling in water.
The structure of the minerals of the smectite group of clay minerals
comprises a 3-layer sheet structure wherein a central octahedral
layer of principally alumina or magnesia is sandwiched between two
tetrehedral layers of principally silica. In the tetrahedral layer,
tetravalent Si is sometimes partly replaced by trivalent Al or Fe.
In the octahedral sheet, there may be a replacement of trivalent
Al by divalent Mg, or of divalent Mg by monovalent lithium atoms.
In the smectite clay minerals where an atom of lower positive valence
replaces one of higher valence, there results within the clay structure
deficit of positive charge, or, in other words, an excess of negative
charge. This excess of negative charge is compensated by the adsorption
on the layer surfaces of cations which are too large to be accommodated
within the interior of the crystal structure.
In the presence of water, the compensating cations on the layer
surfaces may be exchanged by other cations when available in solution;
hence they are called "exchangeable cations." The total
amount of these cations can be determined analytically. This amount,
expressed in milliequivalents per 100 gram of dry clay, is called
the "cation exchange capacity" (CEC) or the "base
exchange capacity" (BEC) of the clay.
In the stack of layers which form a smectite particle, the exchangeable
cations are located on each side of each layer in the stack; hence
they are present not only on the exterior surfaces of the particle
but also in between the layers. When smectite clays are contacted
with water or with water vapor, the water molecules penetrate between
the layers. This so-called "interlayer swelling" leads
to at most a doubling of the dry clay volume when four layers of
water are adsorbed. However, for the swelling smectite-type clays
useful in this invention, the swelling process continues and an
amount of water is imbibed which is many times the volume of the
original clay. The additional swelling is a result of the double-layer
repulsive forces between the surfaces of the individual particles,
which pushes them apart. The swelling is called "osmotic swelling"
since the water tends to equalize the high concentration of ions
between any two particles and the low concentrations of ions far
away from the particle surfaces in the bulk aqueous solution. As
a result of this osmotic swelling, the clay/water system becomes
a gel or colloidal solution depending on the concentration of the
clay.
Thus for the purposes of this invention, a clay which exhibits
osmotic swelling in water will have an interlamellar swelling greater
than about 10 angtroms.
The preferred smectite clays which exhibit osmotic swelling are
selected from the group consisting of montmorillonite, hectorite,
beidellite, nontronite, saponite and mixtures thereof, provided
that sufficient of their exchangeable cations are sodium cations
to effect such osmotic swelling. Most particularly preferred is
the montmorillonitic clay found in Wyoming, U.S.A., and variously
called Wyoming bentonite or western bentonite.
The smectite clays which exhibit osmotic swelling (hereinafter
sometimes referred to as "SCWEOS") when contacted with
water, or like aqueous liquid such as urine, immediately swell and
commence hydration. As the surface of each particle contacted swells,
the sorption rate is rapidly decreased and the interior of the particle
sorbs the liquid through a much slower diffusion process. As a result,
the aqueous liquid flows to and contacts further particles until
the liquid is completely sorbed and immobilized. This results in
a low apparent sorption capacity for the SCWEOS which is far less
than the ultimate sorption capacity of the SCWEOS if unrestricted
entry of the aqueous liquid into the interior of the SCWEOS particle
did not occur.
I have now found that the apparent sorption capacity of the SCWEOS
can be synergistically increased by mixing with the SCWEOS a cellulosic
material wherein the weight ratio of the cellulosic material to
the SCWEOS is from about 0.05 to about 3.0. The apparent sorption
capacity of the SCWEOS of this invention is less than 1.0 cc/g.
Thus by the addition of the cellulosic material to the SCWEOS, the
apparent sorption capacity of the mixture is greater than 1.0 cc/g.
Preferably the apparent sorption capacity of the mixture is at least
1.25 cc/g.
The cellulosic materials useful in this invention comprise particulate
materials derived from various agricultural sources, such as grains,
fruits, cotton, vegetables, nuts, trees, grasses, peat, and the
like, and include particulate lignocellulosic materials. Representative
cellulosic materials from grains include oat hulls, corn cobs, cornstalks,
wheat chaf, rice hulls, bagasse, rice bran, and the like. Representative
cellulosic materials from fruits include citrus pulp (from lemons,
oranges, grapefruits, etc.), apple pulp, grape pulp, and the like.
Representative cellulosic materials from cotton include degraded
cotton, cotton burns, cottonseed hulls, and the like. Representative
cellulosic materials from vegetables include beet pulp, tomato pulp,
and the like. Representative cellulosic materials from nuts include
peanut shells, walnut shells, pecan shells, almond shells, and the
like. Representative cellulosic materials from trees include sawdust,
bark, paper, cedar fiber, ground sagebrush, ground kenaf, and the
like. Representative cellulosic materials from grasses include alfalfa,
hay, straw, and the like.
Preferably the cellulosic material is selected from the group consisting
of oat hulls, corn cobs, peanut shells, citrus pulp, beet pulp,
paper, cotton burrs, cottonseed hulls, rice hulls, rice bran, peat,
and mixtures thereof. Most preferably the cellulosic material is
selected from the group consisting of oat hulls, cotton burrs, rice
hulls, peat, and mixtures thereof.
The SCWEOS useful in the cat litter sorbents of this invention
have a particle size distribution such that at least about 95% of
the particles thereof pass through a 2000 micron screen, less than
about 10% of its particles pass through a 149 micron screen, and
at least about 80% of its particles are retained on a 297 micron
screen. Preferably at least about 90% of the particles of the SCWEOS
are within the range from about 250 microns to about 2000 microns,
i.e., preferably at least 90% of the particles pass through a 2000
micron screen and are retained on a 250 micron screen.
The particle size of the cellulosic material useful in this invention
is dependent upon the particle size of the SCWEOS. Thus the cellulosic
material must have a particle size distribution that would prevent
adverse separation of the particles of cellulosic material and the
particles of the SCWEOS. If the cellulosic material and SCWEOS are
dry mixed, then the cellulosic material useful in the cat litter
sorbents of this invention have a particle size distribution such
that at least about 95% of the particles thereof pass through a
2000 micron screen, at least about 65% of its particles are retained
on a 297 micron screen, and less than about 10% of its particles
pass through a 149 micron screen. Preferably at least about 90%
of its particles are within the range from about 250 microns to
about 2000 microns.
For other uses of the SCWEOS/cellulosic material dry blends, other
particle size distributions may be used. Thus when the SCWEOS is
a pulverized clay wherein at least about 90% of the particles thereof
are less than 149 microns, the particle size of the cellulosic material
should be similar, i.e., at least about 90% of the particles thereof
should pass through a 149 micron screen.
Thus in the broadest aspects of the invention, the particle size
of the SCWEOS and the cellulosic material need only be such that
at least about 95% of their particles be less than about 2000 microns.
When the apparent sorption capacity of the SCWEOS is increased
by mixing therewith the cellulosic material and an aqueous liquid,
such as water, a surfactant solution, and the like, the particle
size distribution of the SCWEOS and the cellulosic material are
not as critical since the particles of SCWEOS swell and bind the
cellulosic material particles thereto. Upon drying of the mixture,
as desired, the particles of the mixture can be separated by sieving
or other means to obtain the desired particle size distribution.
In this process, when the particles are used as a cat litter, the
particles greater than 2000 microns can be crushed and returned
to the sieving operation, and the particles less than 149 microns
or any other desired lower limit of particle size, such as 250 microns,
can be recycled to the mixing operation wherein they are again mixed
and contacted with the aqueous liquid.
Thus it is another aspect of this invention to provide a method
of preparing a sorbent which comprises mixing a SCWEOS which has
a particle size such that at least about 95% of the particles thereof
pass through a 2000 micron screen with a particulate cellulosic
material having a particle size such that at least about 95% of
the particles thereof pass through a 2000 micron screen and an aqueous
liquid, wherein the weight ratio of the cellulosic material to the
smectite clay is in the range from about 0.05 to about 3.0 adjusting
the mixture, such as by drying, to the desired moisture content,
and sieving the sorbent to the desired particle size distribution.
When the sorbent is used as a cat litter, preferably the sorbent
will have a particle size distribution such that at least about
95% of its particles pass through a 2000 micron screen, at least
about 80% of its particles are retained on a 297 micron screen,
and less than about 10% of its particles pass through a 149 micron
screen. The concentration of aqueous liquid should be such that
the wet mixture can be easily handled in the mixing equipment utilized.
Preferably the aqueous liquid will be present in the wet mixture
in an amount from about 10% to about 50% by weight of the wet mixture.
The sorbents prepared by this process appear much more homogeneous
as compared to the sorbents prepared by dry mixing the SCWEOS with
the cellulosic materials.
The aqueous liquid may contain one or more materials to provide
the sorbent with additional or enhanced properties not obtainable
in the absence of such material or materials. Thus the aqueous liquid
may contain a surfactant to enhance the rate of sorption of the
sorbent or to further increase the sorption capacity of the sorbent.
Either nonionic, anionic, or cationic surfactants may be used. Exemplary
surfactants are well known in the chemical arts. The aqueous liquid
may contain odorants, bactericides, fungicides, attractants, colorants,
and the like materials.
The sorbents of this invention have the property that when the
sorbent is wetted with an aqueous liquid, the wetted sorbent has
sufficient cohesiveness for removal of the wetted sorbent from the
nonwetted sorbent particles. Thus, for instance, in a cat litter
box, the sorbent when wetted with urine forms a mass of sorbed,
wetted sorbent that can be scooped out or otherwise removed from
the litter box. The cohesiveness of the sorbents of this invention
is dependent upon the concentration of the SCWEOS in the sorbent.
The sorbent should contain a minimum of 30% by weight of the SCWEOS,
preferably at least 35% by weight, and most preferably at least
40% by weight. Furthermore, the preferred sorbents of this invention
have the property that the wetted sorbent, upon its removal from
the nonwetted sorbent, will disintegrate over time when placed in
water. When used as a cat litter, this enables the wetted litter
to be flushed down a toilet (provided the toilet does not exit into
a septic system for treatment). The disintegration of the wetted
sorbent or litter is primarily dependent upon the maximum concentration
of SCWEOS in the sorbent. Thus the sorbent should contain a maximum
concentration of 80% by weight of the SCWEOS, preferably less than
about 75%, most preferably not more than about 70%. At concentrations
greater than about 80% of the SCWEOS, the lump of wetted sorbent
hydrates further into a mass which does not disintegrate in water
over time. Thus the clumping cat litter sorbents of this invention
will contain from about 30% to about 80% by weight of the SCWEOS,
preferably from about 35% to about 75%, and most preferably from
about 40% to about 70% by weight.
The preferred sorbents of this invention which comprise a clumping
litter box sorbent have a bulk density in the range from about 0.54
g/cc to about 0.96 g/cc, preferably from about 0.60 g/cc to about
0.90 g/cc, and most preferably from about 0.66 g/cc to about 0.90
g/cc. As discussed hereinbefore, the cellulosic material synergistically
increases the apparent sorption capacity of the SCWEOS. The apparent
sorption capacity of the cat litter sorbents of this invention should
be greater than about 1.0 cc water per gram of sorbent, preferably
at least about 1.25 cc/g.
In order to obtain the desired bulk density in the clumping litter
box sorbent of the invention, there may be mixed with the SCWEOS
and the cellulosic material a density control agent. Preferably
the density control agent is an inorganic substance which does not
exhibit osmotic swelling. Most preferably the density control agent
has a bulk density which is intermediate the bulk density of the
SCWEOS and the bulk density of the cellulosic material. The most
preferred density control agent is a clay or clay-like material
which does not exhibit osmotic swelling. Representative clays are
smectite clays wherein the concentration of exchangeable divalent
or trivalent cations is such that the clay does not exhibit osmotic
swelling, such as calcium montmorillonite or bentonite, or which
has too low a base exchange capacity to exhibit osmotic swelling.
Other clays useful as density control agents are attapulgite, sepiolite,
fullers earth, halloysite, illite, mixed layer clays, chlorite,
kaolinite, mica, vermiculite, and the like. Clay-like materials
which are useful as density control agents include diatomaceous
earth, zeolites, wollastonite, talc, perlite, and the like. Other
materials such as fly ash, alkaline earth metal carbonates, borates,
phosphates, etc. may be used. The density control agent may be a
synthetic sorbent such as the sorbents set forth in the following
U.S. Patents, incorporated herein by reference: U.S. Pat. Nos. 4163674
(Been); 4183763 (Omilinsky et al.); 4264543 (Valenta); 4275684
(Kramer et al.); 4395357 (Kramer et al.); 4724242 (Vassileff);
4736706 (Lang); 4824810 (Lang et al.); and 4925826 (Hamm et
al.).
The particle size of the density control agent is dependent upon
the particle sizes of the SCWEOS and the cellulosic material. Thus
the density control agent must have a particle size distribution
that would prevent adverse separation of the particles of the density
control agent from the particles of the SCWEOS and the cellulosic
material. Thus the density control agent will have a particle size
distribution such that at least 95% of the particles thereof pass
through a 2000 micron screen, at least about 80% of its particles
are retained on a 250 micron screen, and less than about 10% of
its particles pass through a 149 micron screen when the sorbent
is prepared by dry mixing. In the broadest aspect of this invention,
the density control agent has a particle size such that at least
about 95% of the particles thereof pass through a 2000 micron screen.
The bulk density and apparent sorption capacity required in the
clumping cat litter sorbents of this invention are obtained by mixing
with the desired amount of SCWEOS as set forth hereinbefore sufficient
cellulosic material to provide from about 5% to about 70% by weight,
preferably from about 5% to about 50% by weight, and most preferably
from about 5% to about 30% by weight, and sufficient density control
agent to provide from 0% to about 60% by weight, preferably from
0% to about 50%, most preferably from about 5% to about 50% by weight.
In order to more completely describe the invention, the following
nonlimiting examples are given. In these examples and throughout
this specification, the following abbreviations may be used: BD=compacted
bulk density; SC=water sorption capacity; cc=cubic centimeter(s);
g=gram(s); lbm=pound. All mesh sizes used in the description of
the invention are in terms of U.S. Standard Sieve Series, Fine Series
of 1940 i.e., 10 mesh=2000 microns sieve openings, 50 mesh=297
microns, 60 mesh=250 microns, 100 mesh=149 microns. A particle size
designated +X indicates the particles were retained on a sieve of
size X mesh. A particle size of Y/Z indicates that the particles
passed through a sieve of mesh size Y and were retained on a sieve
of mesh size Z. A particle size designated -W indicates that the
particles all passed through a sieve of mesh size W.
The particle size distribution, the bulk density, and the water
sorption capacity of the various materials evaluated in the Examples
is set forth in Table A. All percentages throughout the Tables,
Examples, and this specification are weight percent. The particle
size of the materials was determined using the following procedure:
A series of sieves of varying mesh sizes with openings diminishing
in size from the top downward were stacked over a solid bottom pan.
The materials were placed on a vibrating shaker and shaken for 10
minutes. The weight of material retained on each sieve and in the
pan was determined and the % by weight of sample calculated.
Methods are known to measure the compacted bulk density of solids.
In these examples, the material was weighed into a 100 cc graduate
cylinder, compacted by tapping to constant volume, and measuring
the volume of the compacted solids. The apparent sorption capacity
for the purposes of describing and claiming this invention, is measured
using the following procedure: a measured quantity of the sorbent
is weighed into a preweighed or tared plastic weighing dish, generally
5.0 grams of sample; distilled water is added dropwise slowly until
2.5 grams (cc) has been added; the wetted sorbent is then covered
with additional dry sorbent, generally 5.0 grams; this is aged five
(5) minutes to allow for sorption and spreading of the water; thereinafter
the weight of the sample not wet by the water is determined by carefully
pouring off the dry sample from the wetted sample; the sorption
capacity in cc/g is calculated using the equation
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