WO1989002698A1 - Absorbent composition, and method of making same - Google Patents
Absorbent composition, and method of making same Download PDFInfo
- Publication number
- WO1989002698A1 WO1989002698A1 PCT/US1988/003370 US8803370W WO8902698A1 WO 1989002698 A1 WO1989002698 A1 WO 1989002698A1 US 8803370 W US8803370 W US 8803370W WO 8902698 A1 WO8902698 A1 WO 8902698A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- cyclodextrin
- clay
- absorbent composition
- nitrogenous compound
- weight
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 68
- 230000002745 absorbent Effects 0.000 title claims abstract description 49
- 239000002250 absorbent Substances 0.000 title claims abstract description 49
- 238000004519 manufacturing process Methods 0.000 title abstract description 5
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 claims abstract description 102
- 229920000858 Cyclodextrin Polymers 0.000 claims abstract description 99
- 239000004927 clay Substances 0.000 claims abstract description 68
- -1 nitrogenous compound Chemical class 0.000 claims abstract description 29
- 239000006096 absorbing agent Substances 0.000 claims abstract description 25
- 239000000463 material Substances 0.000 claims abstract description 24
- 241001465754 Metazoa Species 0.000 claims abstract description 20
- 229920000642 polymer Polymers 0.000 claims abstract description 13
- 239000011159 matrix material Substances 0.000 claims abstract description 10
- 229920000058 polyacrylate Polymers 0.000 claims abstract description 8
- 239000003205 fragrance Substances 0.000 claims description 40
- 238000000034 method Methods 0.000 claims description 32
- 239000011230 binding agent Substances 0.000 claims description 23
- 239000000853 adhesive Substances 0.000 claims description 21
- 230000001070 adhesive effect Effects 0.000 claims description 21
- 239000002245 particle Substances 0.000 claims description 13
- 239000007788 liquid Substances 0.000 claims description 9
- 239000006185 dispersion Substances 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 6
- 239000000843 powder Substances 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 229920000223 polyglycerol Polymers 0.000 claims description 2
- 238000005507 spraying Methods 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 abstract description 10
- 239000002253 acid Substances 0.000 abstract description 4
- 235000015112 vegetable and seed oil Nutrition 0.000 abstract description 3
- 239000008158 vegetable oil Substances 0.000 abstract description 3
- 239000003208 petroleum Substances 0.000 abstract description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 241000219823 Medicago Species 0.000 description 6
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 5
- 239000005909 Kieselgur Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
- 235000019698 starch Nutrition 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 229920002907 Guar gum Polymers 0.000 description 3
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 3
- 241000209504 Poaceae Species 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 229960000892 attapulgite Drugs 0.000 description 3
- 229910000278 bentonite Inorganic materials 0.000 description 3
- 239000000440 bentonite Substances 0.000 description 3
- 229940092782 bentonite Drugs 0.000 description 3
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 229940097362 cyclodextrins Drugs 0.000 description 3
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 3
- 239000000665 guar gum Substances 0.000 description 3
- 235000010417 guar gum Nutrition 0.000 description 3
- 239000008108 microcrystalline cellulose Substances 0.000 description 3
- 229940016286 microcrystalline cellulose Drugs 0.000 description 3
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 3
- 229910052901 montmorillonite Inorganic materials 0.000 description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
- 231100000252 nontoxic Toxicity 0.000 description 3
- 230000003000 nontoxic effect Effects 0.000 description 3
- 229910052625 palygorskite Inorganic materials 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- 210000002700 urine Anatomy 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000001116 FEMA 4028 Substances 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- WHGYBXFWUBPSRW-FOUAGVGXSA-N beta-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO WHGYBXFWUBPSRW-FOUAGVGXSA-N 0.000 description 2
- 235000011175 beta-cyclodextrine Nutrition 0.000 description 2
- 229960004853 betadex Drugs 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 235000019804 chlorophyll Nutrition 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000007884 disintegrant Substances 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 229960002154 guar gum Drugs 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 240000008886 Ceratonia siliqua Species 0.000 description 1
- 235000013912 Ceratonia siliqua Nutrition 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 244000303965 Cyamopsis psoralioides Species 0.000 description 1
- 125000003535 D-glucopyranosyl group Chemical group [H]OC([H])([H])[C@@]1([H])OC([H])(*)[C@]([H])(O[H])[C@@]([H])(O[H])[C@]1([H])O[H] 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- 229920000161 Locust bean gum Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 229920001938 Vegetable gum Polymers 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 229910001579 aluminosilicate mineral Inorganic materials 0.000 description 1
- HPTYUNKZVDYXLP-UHFFFAOYSA-N aluminum;trihydroxy(trihydroxysilyloxy)silane;hydrate Chemical compound O.[Al].[Al].O[Si](O)(O)O[Si](O)(O)O HPTYUNKZVDYXLP-UHFFFAOYSA-N 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 230000000843 anti-fungal effect Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 229940099112 cornstarch Drugs 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- ONCZQWJXONKSMM-UHFFFAOYSA-N dialuminum;disodium;oxygen(2-);silicon(4+);hydrate Chemical compound O.[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Na+].[Na+].[Al+3].[Al+3].[Si+4].[Si+4].[Si+4].[Si+4] ONCZQWJXONKSMM-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229910052621 halloysite Inorganic materials 0.000 description 1
- 239000010903 husk Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 229910052622 kaolinite Inorganic materials 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 235000010420 locust bean gum Nutrition 0.000 description 1
- 239000000711 locust bean gum Substances 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229940080314 sodium bentonite Drugs 0.000 description 1
- 229910000280 sodium bentonite Inorganic materials 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000012439 solid excipient Substances 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
- A01K1/00—Housing animals; Equipment therefor
- A01K1/015—Floor coverings, e.g. bedding-down sheets ; Stable floors
- A01K1/0152—Litter
- A01K1/0154—Litter comprising inorganic material
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
- A01K1/00—Housing animals; Equipment therefor
- A01K1/015—Floor coverings, e.g. bedding-down sheets ; Stable floors
- A01K1/0152—Litter
- A01K1/0155—Litter comprising organic material
Definitions
- This invention relates to an abs orbent composition usef u l as an absorbent for aqueous systems, including urine, particularly useful as an improved animal or pet litter composition, and useful as an absorbent for oleophilic materials such as petroleum or vegetable based oils and the like.
- the invention also relates to a method of making the improved absorbent composition and litter compos itions containing same.
- the absorbent composition is comprised of clay and a nitrogenous compound absorber, such as cyclodextrin or other agents which form a matrix system or comp lex similar to cyclodextrin.
- Such other agents include polymerized cyclodextrin and cyclodextrin derivatives and polycarboxylic acid polymers, such as acrylate polymers.
- Natural grasses such as alfalfa have been employed in the past with a clay for a binder. While such natural grasses may contain some odor suppressant ability as a result of any chlorophyl present therein, alfalfa has a strong odor itself, particularly when wet.
- Other materials have been tried along with the alfalfa employing grain or grass straw, such as described in U.S. Patent 4,258,660, which employs clay as a binder for maintaining the ingredients in a pelletized form, rather than for its moisture absorptivity property.
- fragrance releasing additives In order to overcome odor problems, the use of fragrance releasing additives has been suggested as in U.S. patent 3,921,581, which incorporates consolidated particles having the property of fragrance release.
- the particles are composed of a minor amount of a perfume agent and major amount of a solid excipient of molded, finely divided or powdered solids of a binder and water sensitive disintegrant.
- the excipient may be all clay or include other finely divided cellulosic solids, such as sawdust, or chlorophyl containing solids, such as ground alfalfa.
- the binder and water sensitive disintegrant may be water soluble or dispersible gums such as guar gum, microcrystalline cellulose or pregelantinized starch.
- the fragrance release composition is then blended with a porous expanded litter product prepared from equal parts by weight of ground al fa and gelatinized wheat flour.
- an animal litter generally is described which is composed of acidic cellulosic materials which include dried grasses or hay, husks, sawdust, corn cob grits, excelsior and cereal hulls.
- the cellulosic materials are merely ground to a desirable size and sprayed with the acid solution.
- an improved absorbent composition comprised of a cellulosic component, a binder and cyclodextrin as a nitrogenous compound absorber. This provides an effective animal litter product even without addition of a fragrance although the cyclodextrin is also an effective carrier for any desired added aromatic fragrance.
- compositions of this invention retain other desired advantages in that low cost materials are employed, which are non-toxic and which have a reduced odor, even when employed without added fragrance.
- the absorbent composition comprises clay carrying a nitrogenous compound absorber such as cyclodextrin.
- a nitrogenous compound absorber such as cyclodextrin.
- This may be prepared by simple admixing of the cyclodextrin and the clay particles.
- the cyclodextrin will be present either as a surface coating or is incorporated internally into the clay base or substrate dependent on the method of preparation of the product.
- a liquid dispersion of the cyclodextrin may be applied, i.e , by spraying an aqueous disperson of the cyclodextrin on to the clay particles.
- an adhesive may be employed in order to ensure adherence of the cyclodextrin to the clay.
- the clay after mixing, is crushed to an appropriate particle size and coated with a liquid application of an adhesive or binder followed by application of a dry, cyclodextrin powder which adheres to the clay through the adhesive applied.
- a kiln dried clay is generally employed.
- the cyclodextrin is added to the resulting clay slurry or mud and the cyclodextrin is incorporated internally into the clay.
- the clay is mixed in a slurry form containing water sometimes referred to as a "mud.”
- the cyc lodextrin is added to the mud product at the desired level.
- the clay slurry or mud containing the cyclodextrin is then dried or baked and subsequently crushed or broken into the appropriate particle size. In this method no adhesive is usually necessary.
- the invention concerns an absorbent composition particularly adapted for use as an animal litter comprised of clay and a nitrogenous compound absorber such as cyclodextrin or other agents having a matrix system similar to cyclodextrin.
- a nitrogenous compound absorber such as cyclodextrin or other agents having a matrix system similar to cyclodextrin.
- the invention also concerns methods of preparing such an absorbent composition.
- the major component of the absorbent composition of the present invention is clay or clay like materials.
- Clay as the term is used herein, is intended to encompass the usual aluminosilicate minerals, such as kaolinite, halloysite, attapulgite, montmori llonite, vermiculite hectori te and the like, as well as diatomaceous earth or Fuller's earth.
- the matrix of the cyclodextrin in combination with the expanding crystal lattice of the clay material such as bentonite powder a particularly desirable and effective absorbent composition.
- diatomaceous earth and attapulgite are also commonly employed in animal litter and are desirable materials.
- Diatomaceous earth is generally available commercially as a kiln-dried material resulting from a mined product containing about 20% moisture.
- MontmoriUonite is generally supplied as a rotary kiln-dried product resulting from a mined product containing about 35 to 40% moisture and is kiln dried commercially to a moisture content of about 8 to 9% .
- the substantial ly dry clays will contain about 10 to 15% moisture with 10% or less being preferred.
- Cyclodextrins are the preferred ingredient for control of odor as a nitrogenous compound absorber or selective entrapment agent.
- the cyclodextrins are cyclic oligosaccharides that contain at least six ⁇ -1,4 linked D glucopyranose units.
- ⁇ -Cyclodextrin has 7 units, while ⁇ and v have 6 and 8 respectively.
- Cyclodextrins have the shape of a hollow truncated cone with primary and secondary hydroxy groups crowning opposite ends of the torus. The inside of the molecule provides an ability to admit various guest molecules into the inner cavity. The formation of an inclusion complex with the cyclodextrin will depend on the relative size and ionic nature of the guest molecule. While net wishing to be limited thereto, it is believed that nitrogenous compounds are absorbed as a guest molecule in the inner cavity of the cyclodextrin.
- cyclodextrin is the preferred material
- other materials which form a matrix or complex similar to cyclodextrin may be employed in similar manner to act as the nitrogenous compound absorber.
- Compounds having a matrix, or forming a complex similar to cyclodextrin include cyclodextrin derivatives and various polymers which are inert and non-toxic.
- cyclodextrin derivatives which may be employed are cyclodextrin carbamates (such as shown in U.S. Patent 3459732) and the cyclodextrin polyol ether or polyethers (such as described in U.S. Patents 3453259 and 3459731).
- polymers are polymerized ⁇ -cyclodextrin which is available commercially from American Maize. Synthetic or plastic polymers may be employed. Illustrative of these polymers are acrylate polymers such as sold by wickhen Products under the name POLYTRAP R . One such product is POLYTRAP 603. These products are described by the supplier as fully thermoset crosslinked acrylate polymers which are non-toxic and capable of entrapping a fragrance. Some of the copolymers are specifically described as polyglycerol acrylate and polypropyl acrylate. The polymers are generally polycarboxylic polymers consisting of monomer units of acrylic acid or metnacrylic acid. Generally the carboxyl groups are esterified at least in part.
- alkyl esters i.e. methyl, ethyl, propyl and butyl, and the glycerol esters are preferred.
- macromolecular compounds which are partially structured of monomer units with a free carboxylic acid group are highly polymerized co-polymerizates of acrylic acid and/or methacrylic acid with acrylic or methacrylic acid esters.
- the polymerisates may be obtained in powder form as well as an aqueous dispersion.
- These acrylate co-polymers are capable of carrying more fragrance than cyclodextrin and are accordingly generally employed in a smaller amount. This property is also believed to provide for slow fragrance release where a fragrance is added to the composition.
- fragrance which does not materially affect the basic litter composition of cellulosic materials and binder, will generally be included in the composition.
- Fragrances employed are natural or synthetic aromatic volatile compounds generally employed as a fragrance by those skilled in the fragrance art.
- the nitrogen absorbing compound or ingredient will be employed in an amount of up to about 2% by weight of the total litter composition, however, it is desirable not to exceed about 1%, and generally from 0.05 to about 0.5%, preferably about 0.1% is employed.
- the cyclodextrin is present at about 0.1% by weight of the clay.
- the cyclodextrin may carry a 10% fragrance load, which at a 1% level of cyclodextrin would provide about 0.1% fragrance based on total composition.
- the fragrance level will accordingly be about 0.01% of the total composition, which is the preferred level of fragrance where such is employed.
- fragrance may load fragrance at a higher level than cyclodextrin.
- polymer systems may be capable of loading as high as 60% fragrances.
- the acrylate copolymers noted above are capable of carrying about 6 times more fragrance than cyclodextrin and according ly may be employed in about one-sixth the amount required when cyclodextrin, or a cyclodextrin derivative, is employed. It is however preferred that the fragrance level be maintained at a level of about 0.01% fragrance based on total composition and, accordingly, the amount of such polymer system will be adjusted to provide that level of fragrance.
- fragrance is carried by the cyclodextrin it may be incorporated into the cyclodextrin before application of the cyclodextrin to the clay.
- fragrance or essence may be added by simple addition to the cyclodextrin-clay product during the bagging or packaging operation.
- periodic injections of the fragrance or essence is injected during the packaging operation of the dry litter absorbent composition which consists essentially of the clay and cyclodextrin.
- a liquid adhesive or binder is first applied to the clay so as to bind or adhere the cyclodextrin to the clay.
- binders or adhesives may be applied in the form of aqueous solutions or dispersions of the adhesive or binder.
- aqueous solutions employed will generally be solutions containing from 2.5 to 7% by weight of the adhesive. A 5% solution is generally preferred.
- the aqueous solution is applied at a rate so as to apply to the clay from about 0.25 to about 0.7% by weight of adhesive based on the clay, with about 0.5% preferred.
- the clay surface may be merely wetted with water, or other liquid and the cyclodextrin applied. Further a thin or dilute dispersion of a clay itself may be applied and function as a binder for the cyclodextrin.
- the adhesive or binder include the water soluble or dispersible products such as the vegetable gums like the polygalactomannan gums, i.e. guar gum and locust bean being the most common.
- the binder may also be an alginate or xanthan gum, a pregelatinze c starch such as pregelatinized cornstarch or microcrystalline cellulose polymers.
- the clay is the major or principal ingredient of the absorbent composition and accordingly the clay will comprise about 90%, and generally 95% or more by weight of the composition.
- the clay will accordingly comprise in excess of 99% by weight of the total composition, i.e., about 99.8 to 99.9%.
- an adhesive or binder is employed the clay will comprise about 99 to 99.5%.
- Other absorbent materials may be employed in addition to the clay if desired. Such are known to those skilled in the art. When such are employed, however, the clay absorbent should be employed in a major amount not less than 50% by weight of the total absorbent composition.
- the process of preparing the absorbent composition may generally be described as comprising adding to an absorbent clay a nitrogenous compound absorber such as cyclodextrin in an amount of about 0.05 to 2% by weight, preferrably about 0.1%.
- the cyclodextrin is applied in the form of a dry powder after application to the clay of an adhesive or binder in liquid form, i.e., an aqueous solution.
- the clay has been previously crushed or ground to a size of about 2 to 7mm.
- the aqueous adhesive solution is sprayed on the clay particles and subsequently tumbled with the dry, powdered cyclodextrin. In the examples to follow this will be referred to as Method A.
- the cyclodextrin is added to a clay slurry or mud after which the clay containing the cyclodextrin incorporated therein is dried and crushed or ground to the desired particle size of about 2 to 7mm. This method will be referred to as Method B.
- composition prepared in accord with Method A would be comprised as follows: Clay about 99.5%
- Adhesive about 0.4% Cyclodextrin about 0.1% The preferred composition prepared by Method B would not have present the adhesive or binder would accordingly be comprised of about 99.9% clay and about 0.1% cyclodextrin.
- the same composition may be achieved by the simple admixing of dry cyclodextrin and dry clay particles in the amounts indicated, which may be referred to as Method C.
- Method D an aqueous dispersion of the cyclodextrin is sprayed, or otherwise applied to the clay, to provide the amount of cyclodextrin indicated after which the product is dried and packaged.
- aqueous solutions should not be employed, or should be avoided, when a fragrance is carried by the cyclodextrin as the cyclodextrin may prematurely release the fragrance in the presence of water.
- other liquids may be employed in the solution or dispersion applications methods.
- Such other liquids would be glycols or alcohols such as propylene glycol; and glycerin or vegetable oils.
- the preferred clays are the bentonite or montmoril lonite clays, attapulgite and diatomaceous earth.
- the preferred adhesive are guar or locust bean gum, pregelatinzed starches or microcrystalline cellulose polymers.
- the samples of the present invention have virtually no odor in the absence of fragrance.
- the fragrance employed will of course determine the type of odor.
- the samples of the absorbent composition of the present invention will entrap or absorb the nitrogenous compounds, when about 0.1% cyclodextrin is incorporated into the composition, and larger amounts of cyclodextrin appear unnecessary. If the cyclodextrin derivatives are employed in place of the cyclodextrin in the formulations noted, these are employed in amounts at about the same level as cyclodextrin.
- the POLYTRAP acrylate polymers described earlier as these can carry a higher load, the compounds are generally employed in a smaller amount, preferably on the order of 1% or less, i.e. 0.05% to 0.1%.
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Abstract
An absorbent composition is disclosed which is particularly useful as an improved animal or pet litter composition, or as an absorbant for aqueous systems or oleophilic materials such as petroleum or vegetable oils and the like. Also disclosed is a method of making the improved absorbent composition and litter composition containing same. The absorbent composition is comprised of clay and a nitrogenous compound absorber, such as cyclodextrin or other agents which form a matrix system or complex similar to cyclodextrin. Such other agents include polymerized cyclodextrin and cyclodextrin derivatives and polycarboxylic acid polymers such as acrylate polymers.
Description
ABSORBENT COMPOSITION, AND METHOD OF MAKING SAME
BACKGROUND OF THE INVENTION
Fi eld of the Invention
This invention relates to an abs orbent composition usef u l as an absorbent for aqueous systems, including urine, particularly useful as an improved animal or pet litter composition, and useful as an absorbent for oleophilic materials such as petroleum or vegetable based oils and the like. The invention also relates to a method of making the improved absorbent composition and litter compos itions containing same. The absorbent composition is comprised of clay and a nitrogenous compound absorber, such as cyclodextrin or other agents which form a matrix system or comp lex similar to cyclodextrin. Such other agents include polymerized cyclodextrin and cyclodextrin derivatives and polycarboxylic acid polymers, such as acrylate polymers.
Description of Related Art
Many attempts have been made in the past to provide improved absorbent compositions which are acceptable for use in animal litters, particularly for domestic pets such as cats. Generally known litter compositions available today contain large amounts of clay and/or natural grass compositions. In addition to being useful as animal
litter compositions, such compositions containing clays have also been suggested for use in absorbi ng oily materials commonly found in garage floors from automobiles. Such oleophilic or oily materials include the lubricating oils, kerosene, power steering fluids, transmission fluids and spills from gasoline and ethylene glycol antifreeze coolant compositions and spills of vegetable oils in food plants, such as when frying. Such compositions containing clays have not been entirely satisfactory and have been deficient in one or more of the characteristics and properties necessary as an effective absorbent, particularly for animal litter applications, where odor suppression or elimination is desirable.
The desirable characteristics of an absorbent composition for animal litters include:
(a) high absorptive ability, particularly water or high moisture absorbency;
(b) a reduced odor, particularly ammoniacal from urine waste products;
(c) lack of toxicity;
(d) low degree of dusting to avoid tracking; (e) and low cost, economically available ingredients of the composition. Natural grasses, such as alfalfa have been employed in the past with a clay for a binder. While such natural grasses may contain some odor suppressant ability as a result of any chlorophyl present therein, alfalfa has a strong odor itself, particularly when wet. Other materials have been tried along with the alfalfa employing grain or grass straw, such as described in U.S. Patent 4,258,660, which employs clay as a binder for maintaining the ingredients in a pelletized form, rather than for its moisture absorptivity property. Other materials have been suggested in the past as a replacement for alfalfa, such as peanut hulls in U.S. Patent 4,217,858, having the characteristics of a lubricant and/or binder. Among those having binder characteristics are clays and lignin such as sodium bentonite. Among the lubricants mentioned is starch. Reference is also made in tne
patent to processed corn cobs having been employed in the past.
In order to overcome odor problems, the use of fragrance releasing additives has been suggested as in U.S. patent 3,921,581, which incorporates consolidated particles having the property of fragrance release. The particles are composed of a minor amount of a perfume agent and major amount of a solid excipient of molded, finely divided or powdered solids of a binder and water sensitive disintegrant. The excipient may be all clay or include other finely divided cellulosic solids, such as sawdust, or chlorophyl containing solids, such as ground alfalfa. In addition to clays, the binder and water sensitive disintegrant may be water soluble or dispersible gums such as guar gum, microcrystalline cellulose or pregelantinized starch. The fragrance release composition is then blended with a porous expanded litter product prepared from equal parts by weight of ground al fa and gelatinized wheat flour.
In U.S. Patent 3,059,615, an animal litter generally is described which is composed of acidic cellulosic materials which include dried grasses or hay, husks, sawdust, corn cob grits, excelsior and cereal hulls. The cellulosic materials are merely ground to a desirable size and sprayed with the acid solution.
Other patents generally dealing with alfalfa-based animal litter with various binders, either alone or admixed with other absorbent materials are described in U.S. Patents 4,206,718; 3,923,005; 3,972,971; 3 , 789 , 797 and U.S. Patent 3,983,842, which describes other prior patents in the litter area. Still other patents generally dealing with animal litters, including some containing clays as the major absorbent material such as U.S. Patent 8,375,734; or further U.S. Patents 4,407,231; 2,014,900; 4,386,580; 4,405,354; 4,424,763; 4,085,704; 3,916,831; 3,636,927; 4,157,696 and 4,341,180. In our copending U.S. application Serial No. 906966 filed September
22, 1986 for Absorbent Composition, Method of Making and Using Same (Attorney Docket 1.002), there is disclosed an improved absorbent composition comprised of a cellulosic component, a binder and cyclodextrin as a nitrogenous compound absorber. This provides an
effective animal litter product even without addition of a fragrance although the cyclodextrin is also an effective carrier for any desired added aromatic fragrance.
SUMMARY OF THE INVENTION
It has now been discovered that cyclodextrin, or materials or other agents which form a matrix system similar to cyclodextrin also forms an effective odor control with clay or soil based animal litter absorbent composition. Further, the compositions of this invention retain other desired advantages in that low cost materials are employed, which are non-toxic and which have a reduced odor, even when employed without added fragrance.
Broadly the absorbent composition comprises clay carrying a nitrogenous compound absorber such as cyclodextrin. This may be prepared by simple admixing of the cyclodextrin and the clay particles. The cyclodextrin will be present either as a surface coating or is incorporated internally into the clay base or substrate dependent on the method of preparation of the product. When prepared as a surface coating, a liquid dispersion of the cyclodextrin may be applied, i.e , by spraying an aqueous disperson of the cyclodextrin on to the clay particles. Optionally, an adhesive may be employed in order to ensure adherence of the cyclodextrin to the clay. In the surface coating method employing an adhesive the clay, after mixing, is crushed to an appropriate particle size and coated with a liquid application of an adhesive or binder followed by application of a dry, cyclodextrin powder which adheres to the clay through the adhesive applied.
In the above methods a kiln dried clay is generally employed. In the case where a clay is used resulting from a wet mining process the cyclodextrin is added to the resulting clay slurry or mud and the cyclodextrin is incorporated internally into the clay. In this method incorporating the cyclodextrin internally into the clay, the clay is mixed in a slurry form containing water sometimes
referred to as a "mud." The cyc lodextrin is added to the mud product at the desired level. The clay slurry or mud containing the cyclodextrin is then dried or baked and subsequently crushed or broken into the appropriate particle size. In this method no adhesive is usually necessary.
Accordingly the invention concerns an absorbent composition particularly adapted for use as an animal litter comprised of clay and a nitrogenous compound absorber such as cyclodextrin or other agents having a matrix system similar to cyclodextrin. The invention also concerns methods of preparing such an absorbent composition.
DETAILED DESCRIPTION AND PREFERRED EMBODIMENTS
As noted briefly above, the major component of the absorbent composition of the present invention is clay or clay like materials. Clay, as the term is used herein, is intended to encompass the usual aluminosilicate minerals, such as kaolinite, halloysite, attapulgite, montmori llonite, vermiculite hectori te and the like, as well as diatomaceous earth or Fuller's earth. Particularly desirable ore clays having water expanding crystal lattices, such as bentonite, i.e., montmorillonite, which is a preferred clay material, particularly in the method of preparation in which the cyc lodextrin is incorporated internally when added to a clay mud. While not wishing to be limited thereto, it is believed that the matrix of the cyclodextrin in combination with the expanding crystal lattice of the clay material such as bentonite powder a particularly desirable and effective absorbent composition. However, diatomaceous earth and attapulgite are also commonly employed in animal litter and are desirable materials. Diatomaceous earth is generally available commercially as a kiln-dried material resulting from a mined product containing about 20% moisture. MontmoriUonite is generally supplied as a rotary kiln-dried product resulting from a mined product containing about 35 to 40% moisture and is kiln dried commercially to a moisture content of about 8 to 9% . Thus
the substantial ly dry clays will contain about 10 to 15% moisture with 10% or less being preferred.
Cyclodextrins are the preferred ingredient for control of odor as a nitrogenous compound absorber or selective entrapment agent. The cyclodextrins are cyclic oligosaccharides that contain at least six α-1,4 linked D glucopyranose units. β -Cyclodextrin has 7 units, while α and v have 6 and 8 respectively. Cyclodextrins have the shape of a hollow truncated cone with primary and secondary hydroxy groups crowning opposite ends of the torus. The inside of the molecule provides an ability to admit various guest molecules into the inner cavity. The formation of an inclusion complex with the cyclodextrin will depend on the relative size and ionic nature of the guest molecule. While net wishing to be limited thereto, it is believed that nitrogenous compounds are absorbed as a guest molecule in the inner cavity of the cyclodextrin.
While cyclodextrin is the preferred material, other materials which form a matrix or complex similar to cyclodextrin may be employed in similar manner to act as the nitrogenous compound absorber. Compounds having a matrix, or forming a complex similar to cyclodextrin, include cyclodextrin derivatives and various polymers which are inert and non-toxic. Among the cyclodextrin derivatives which may be employed are cyclodextrin carbamates (such as shown in U.S. Patent 3459732) and the cyclodextrin polyol ether or polyethers (such as described in U.S. Patents 3453259 and 3459731). Among suitable polymers are polymerized β -cyclodextrin which is available commercially from American Maize. Synthetic or plastic polymers may be employed. Illustrative of these polymers are acrylate polymers such as sold by wickhen Products under the name POLYTRAPR. One such product is POLYTRAP 603. These products are described by the supplier as fully thermoset crosslinked acrylate polymers which are non-toxic and capable of entrapping a fragrance. Some of the copolymers are specifically described as polyglycerol acrylate and polypropyl acrylate. The polymers are generally polycarboxylic polymers consisting of monomer units of acrylic acid or metnacrylic acid. Generally the carboxyl groups are esterified at least in part. In
particular the alkyl esters, i.e. methyl, ethyl, propyl and butyl, and the glycerol esters are preferred. Examples of macromolecular compounds which are partially structured of monomer units with a free carboxylic acid group are highly polymerized co-polymerizates of acrylic acid and/or methacrylic acid with acrylic or methacrylic acid esters. The polymerisates may be obtained in powder form as well as an aqueous dispersion. These acrylate co-polymers are capable of carrying more fragrance than cyclodextrin and are accordingly generally employed in a smaller amount. This property is also believed to provide for slow fragrance release where a fragrance is added to the composition. While addition of a fragrance is not necessary, users of animal litters have become accustomed to the use of fragrances in commercial animal litters, and accordingly, the addition of a fragrance, which does not materially affect the basic litter composition of cellulosic materials and binder, will generally be included in the composition. Fragrances employed are natural or synthetic aromatic volatile compounds generally employed as a fragrance by those skilled in the fragrance art.
The nitrogen absorbing compound or ingredient will be employed in an amount of up to about 2% by weight of the total litter composition, however, it is desirable not to exceed about 1%, and generally from 0.05 to about 0.5%, preferably about 0.1% is employed. In the present invention, since the clay comprises the major portion of the total composition, the cyclodextrin is present at about 0.1% by weight of the clay. Where a fragrance is employed, the cyclodextrin may carry a 10% fragrance load, which at a 1% level of cyclodextrin would provide about 0.1% fragrance based on total composition. At a 0.1% cyclodextrin level, the fragrance level will accordingly be about 0.01% of the total composition, which is the preferred level of fragrance where such is employed. Other ingredients used as nitrogenous absorbers or selective entrapment and fragrance release agents may load fragrance at a higher level than cyclodextrin. For example, polymer systems may be capable of loading as high as 60% fragrances. Thus, the acrylate copolymers noted above are capable of carrying about 6 times more fragrance than cyclodextrin and according ly may be employed in about one-sixth the
amount required when cyclodextrin, or a cyclodextrin derivative, is employed. It is however preferred that the fragrance level be maintained at a level of about 0.01% fragrance based on total composition and, accordingly, the amount of such polymer system will be adjusted to provide that level of fragrance. Where the fragrance is carried by the cyclodextrin it may be incorporated into the cyclodextrin before application of the cyclodextrin to the clay. However, fragrance or essence may be added by simple addition to the cyclodextrin-clay product during the bagging or packaging operation. Thus, periodic injections of the fragrance or essence is injected during the packaging operation of the dry litter absorbent composition which consists essentially of the clay and cyclodextrin.
Other materials may be added, which do not materially affect the basic composition such as bacteriostats, dyes, anti-fungal, disinfectants, expansion and anti-dusting agents and the like.
As indicated earlier, particularly in the method of preparation of a cyclodextrin surface coated clay product employing a dry powdered cyclodextrin, a liquid adhesive or binder is first applied to the clay so as to bind or adhere the cyclodextrin to the clay. These binders or adhesives may be applied in the form of aqueous solutions or dispersions of the adhesive or binder. When water is not desirable in the system, such as, when employing cyclodextrin which carries the fragrance, other liquids may be employed. The aqueous solutions employed will generally be solutions containing from 2.5 to 7% by weight of the adhesive. A 5% solution is generally preferred. The aqueous solution is applied at a rate so as to apply to the clay from about 0.25 to about 0.7% by weight of adhesive based on the clay, with about 0.5% preferred. Alternatively, the clay surface may be merely wetted with water, or other liquid and the cyclodextrin applied. Further a thin or dilute dispersion of a clay itself may be applied and function as a binder for the cyclodextrin.
The adhesive or binder include the water soluble or dispersible products such as the vegetable gums like the polygalactomannan gums, i.e. guar gum and locust bean being the most common. The binder may also be an alginate or xanthan gum, a pregelatinze c starch such as
pregelatinized cornstarch or microcrystalline cellulose polymers.
As indicated above the clay is the major or principal ingredient of the absorbent composition and accordingly the clay will comprise about 90%, and generally 95% or more by weight of the composition. When cyclodextrin is employed alone, or with fragrance, at the preferred level of about 0.1% the clay will accordingly comprise in excess of 99% by weight of the total composition, i.e., about 99.8 to 99.9%. When an adhesive or binder is employed the clay will comprise about 99 to 99.5%. Other absorbent materials may be employed in addition to the clay if desired. Such are known to those skilled in the art. When such are employed, however, the clay absorbent should be employed in a major amount not less than 50% by weight of the total absorbent composition. The process of preparing the absorbent composition may generally be described as comprising adding to an absorbent clay a nitrogenous compound absorber such as cyclodextrin in an amount of about 0.05 to 2% by weight, preferrably about 0.1%.
In one method the cyclodextrin is applied in the form of a dry powder after application to the clay of an adhesive or binder in liquid form, i.e., an aqueous solution. The clay has been previously crushed or ground to a size of about 2 to 7mm. The aqueous adhesive solution is sprayed on the clay particles and subsequently tumbled with the dry, powdered cyclodextrin. In the examples to follow this will be referred to as Method A.
In a second method, the cyclodextrin is added to a clay slurry or mud after which the clay containing the cyclodextrin incorporated therein is dried and crushed or ground to the desired particle size of about 2 to 7mm. This method will be referred to as Method B.
The preferred composition prepared in accord with Method A would be comprised as follows: Clay about 99.5%
Adhesive about 0.4% Cyclodextrin about 0.1% The preferred composition prepared by Method B would not have present the adhesive or binder would accordingly be comprised of about
99.9% clay and about 0.1% cyclodextrin. The same composition may be achieved by the simple admixing of dry cyclodextrin and dry clay particles in the amounts indicated, which may be referred to as Method C. In still another method, referred to as Method D, an aqueous dispersion of the cyclodextrin is sprayed, or otherwise applied to the clay, to provide the amount of cyclodextrin indicated after which the product is dried and packaged.
Methods employing aqueous solutions should not be employed, or should be avoided, when a fragrance is carried by the cyclodextrin as the cyclodextrin may prematurely release the fragrance in the presence of water. In such a case other liquids may be employed in the solution or dispersion applications methods. Such other liquids would be glycols or alcohols such as propylene glycol; and glycerin or vegetable oils.
The preferred clays are the bentonite or montmoril lonite clays, attapulgite and diatomaceous earth. The preferred adhesive are guar or locust bean gum, pregelatinzed starches or microcrystalline cellulose polymers.
The samples of the present invention have virtually no odor in the absence of fragrance. The fragrance employed will of course determine the type of odor. In use with urine samples, the samples of the absorbent composition of the present invention will entrap or absorb the nitrogenous compounds, when about 0.1% cyclodextrin is incorporated into the composition, and larger amounts of cyclodextrin appear unnecessary. If the cyclodextrin derivatives are employed in place of the cyclodextrin in the formulations noted, these are employed in amounts at about the same level as cyclodextrin. With the POLYTRAP acrylate polymers described earlier, as these can carry a higher load, the compounds are generally employed in a smaller amount, preferably on the order of 1% or less, i.e. 0.05% to 0.1%.
Claims
WE CLAIM: 1. In an absorbent composition comprised of clay as an absorbent material the improvement wherein s aid absorbent contains a nitrogenous compound absorber, said nitrogenous compound absorber being selected from the group consisting of cyclodextrin, cyclodextrin derivatives, polymerized cyclodextrin and polyacrylate compounds having a matrix system similar to cyclodextin.
2. An absorbent composition as defined in Claim 1 wherein said nitrogenous compound absorber is present in an amount of about 0.05 to 2% by weight.
3. An absorbent composition as defined in Claim 1 wherein said nitrogenous compound absorber is cyc lodextrin which is present in an amount of about 0.05 to about 0.5% by weight.
4. An absorbent composition as def ined in Claim 3 wherein said cyclodextrin is present in about 0.1% by weight.
5. An absorbent composition as defined in Claim 4 wherein said cyclodextrin contains up to a 10% by weight load of fragrance.
6. An absorbent composition as defined in Claim 2 wherein said nitrogenous compound absorber is polymerized cyclodextrin.
7. An absorbent composition as defined in Claim 2 wherein said nitrogenous compound absorber is a po lyacrylate polymer selected from the group consisting of polyglycerol acrylate and polypropyl acrylate.
8. An absorbent composition as defined in Claim 1 in which said clay comprises at least 90% by weight of the total absorbent composition.
9. An absorbent composition as defined in Claim 8 in which said clay comprises about 99% by weight of the absorbent composition.
10. An absorbent composition as defined in Claim 1 in which said nitrogenous compound absorber is coated on the clay and adhered thereto with an adhesive binder.
11. A method of preparing an absorbent composition useful as an animal litter having improved odor properties comprising adding to a clay absorbent material a nitrogenous compound absorber in an amount of between 0.05 to 2% by weight, said nitrogenous compound absorber being selected from the group consisting of cyclodextrin, cyclodextrin derivatives, polymerized cyclodextrin and polyacrylate compounds having a matrix system similar to cyclodextrin.
12. A method as defined in Claim 11 wherein an adhesive binder is applied to said clay in liquid form prior to the addition of said nitrogenous compound absorber.
13. A method as defined in Claim 12 wherein said adhesive binder is applied in the form of an aqueous solution sprayed on clay particles having a particle size in the range of about 2 to about 7mm and said nitrogenous compound absorber is cyclodextrin applied in the form of a dry powder which adheres to the clay through said adhesive binder.
14. A method as defined in Claim 13 wherein said cyclodextrin is applied in an amount of about 0.1% by weight.
15. A method as defined in Claim 14 in which said cyclodextrin carries an aromatic volatile fragrance.
16. A method as defined in Claim 11 in which said nitrogenous compound absorber is cyclodextrin and is added to a mud of said clay and mixed with said clay mud so as to incorporate the cyclodextrin internally after which said mixture of clay and cyclodextrin is dried and ground to a particle size in the range of about 2 to about 7mm.
17. A method as defined in Claim 16 in which said cyclodextrin is added to said clay in an amount of about 0.05 to about 0.5% by weight.
18. A method as defined in Claim 17 in which said cyclodextrin is added in an amount of about 0.1% by weight.
19. A method as defined in Claim 11, wherein a dry cyclodextrin is added and mixed with a substantially dry clay.
20. A method as defined in Claim 11, wherein said nitrogenous compound absorber is cyclodextrin and is applied as an aqueous dispersion to a substantially dry clay.
21. A method as defined in Claim 20 wherein said aqueous dispersion of cyclodextrin is applied by spraying.
22. An animal litter having improved odor properties comprising an absorbent composition comprised of clay and a nitrogenous compound absorber, said absorbent composition having a particle size in the range of about 2mm to about 7mm, said nitrogenous compound absorber being selected from the group consisting of cyclodextrin, cyclodextrin derivatives, polymerized cyclodextrin and polyacrylate compounds having a matrix system similar to cyclodextrin.
23. An animal litter as defined in Claim 22 in which said nitrogenous compound absorber is cyclodextrin present in an amount of about 0.05 to about 2% by weight.
24. An animal litter as defined in Claim 23 in which said cyclodextrin is present in an amount of about 0.1% by weight.25. An animal litter as defined in Claim 23 in which said cyclodextrin carries an aromatic volatile fragrance.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/103,927 US4844010A (en) | 1987-10-02 | 1987-10-02 | Absorbent composition, method of making and using same |
US103,927 | 1987-10-02 | ||
US157,913 | 1988-02-19 | ||
US07/157,913 US4881490A (en) | 1988-02-19 | 1988-02-19 | Absorbent composition, and method of making same |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1989002698A1 true WO1989002698A1 (en) | 1989-04-06 |
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Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1988/003370 WO1989002698A1 (en) | 1987-10-02 | 1988-09-30 | Absorbent composition, and method of making same |
Country Status (2)
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WO (1) | WO1989002698A1 (en) |
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US7678367B2 (en) | 2003-10-16 | 2010-03-16 | Kimberly-Clark Worldwide, Inc. | Method for reducing odor using metal-modified particles |
US7754197B2 (en) | 2003-10-16 | 2010-07-13 | Kimberly-Clark Worldwide, Inc. | Method for reducing odor using coordinated polydentate compounds |
US7794737B2 (en) | 2003-10-16 | 2010-09-14 | Kimberly-Clark Worldwide, Inc. | Odor absorbing extrudates |
US7837663B2 (en) | 2003-10-16 | 2010-11-23 | Kimberly-Clark Worldwide, Inc. | Odor controlling article including a visual indicating device for monitoring odor absorption |
US7879350B2 (en) | 2003-10-16 | 2011-02-01 | Kimberly-Clark Worldwide, Inc. | Method for reducing odor using colloidal nanoparticles |
US10214858B2 (en) | 2017-04-13 | 2019-02-26 | Rayonier Performance Fibers, Llc | Cellulosic material with antimicrobial and defiberization properties |
CN114451312A (en) * | 2022-02-16 | 2022-05-10 | 西北师范大学 | Attapulgite-based clay composite cat litter |
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-
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- 1988-09-30 AU AU25540/88A patent/AU2554088A/en not_active Abandoned
- 1988-09-30 WO PCT/US1988/003370 patent/WO1989002698A1/en unknown
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US4009684A (en) * | 1975-11-26 | 1977-03-01 | National Patent Development Corporation | Water soluble polymers useful in the preparation of novel animal litter |
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US4506628A (en) * | 1983-07-13 | 1985-03-26 | Stockel Richard F | Animal litter |
Cited By (36)
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WO1994022501A1 (en) * | 1993-03-31 | 1994-10-13 | The Procter & Gamble Company | Articles containing small particle size cyclodextrin for odor control |
US5939060A (en) * | 1994-08-12 | 1999-08-17 | The Procter & Gamble Company | Composition for reducing malodor impression on inanimate surfaces |
US5578563A (en) * | 1994-08-12 | 1996-11-26 | The Procter & Gamble Company | Composition for reducing malodor impression on inanimate surfaces |
US5593670A (en) * | 1994-08-12 | 1997-01-14 | The Proctor & Gamble Company | Uncomplexed cyclodextrin solutions for odor control on inanimate surfaces |
US5663134A (en) * | 1994-08-12 | 1997-09-02 | The Procter & Gamble Company | Composition for reducing malodor impression on inanimate surfaces |
US5668097A (en) * | 1994-08-12 | 1997-09-16 | The Procter & Gamble Company | Uncomplexed cyclodextrin solutions for odor control on inanimate surfaces |
US5714137A (en) * | 1994-08-12 | 1998-02-03 | The Procter & Gamble Company | Uncomplexed cyclodextrin solutions for odor control on inanimate surfaces |
US5534165A (en) * | 1994-08-12 | 1996-07-09 | The Procter & Gamble Company | Fabric treating composition containing beta-cyclodextrin and essentially free of perfume |
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US6682694B2 (en) | 1994-08-12 | 2004-01-27 | The Procter & Gamble Company | Uncomplexed cyclodextrin solutions for odor control on inanimate surfaces |
US6077318A (en) * | 1994-08-12 | 2000-06-20 | The Procter & Gamble Company | Method of using a composition for reducing malodor impression |
US6287550B1 (en) | 1996-12-17 | 2001-09-11 | The Procter & Gamble Company | Animal care system and litter with reduced malodor impression |
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US6958429B2 (en) | 1998-06-08 | 2005-10-25 | Stockhausen Gmbh & Co. Kg | Water-absorbing polymers with supramolecular hollow molecules, method for producing them and use of the same |
US6358469B1 (en) | 1998-12-01 | 2002-03-19 | S. C. Johnson & Son, Inc. | Odor eliminating aqueous formulation |
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US7645746B1 (en) | 2000-11-13 | 2010-01-12 | The Procter & Gamble Company | Composition for reducing malodor impression on inanimate surfaces |
US7217804B2 (en) | 2001-04-24 | 2007-05-15 | The Procter & Gamble Company | Articles comprising cationic polysaccharides and acidic pH buffering means |
US7666410B2 (en) | 2002-12-20 | 2010-02-23 | Kimberly-Clark Worldwide, Inc. | Delivery system for functional compounds |
US7582308B2 (en) | 2002-12-23 | 2009-09-01 | Kimberly-Clark Worldwide, Inc. | Odor control composition |
US7413550B2 (en) | 2003-10-16 | 2008-08-19 | Kimberly-Clark Worldwide, Inc. | Visual indicating device for bad breath |
US7488520B2 (en) | 2003-10-16 | 2009-02-10 | Kimberly-Clark Worldwide, Inc. | High surface area material blends for odor reduction, articles utilizing such blends and methods of using same |
US7582485B2 (en) | 2003-10-16 | 2009-09-01 | Kimberly-Clark Worldride, Inc. | Method and device for detecting ammonia odors and helicobacter pylori urease infection |
US7438875B2 (en) | 2003-10-16 | 2008-10-21 | Kimberly-Clark Worldwide, Inc. | Method for reducing odor using metal-modified silica particles |
US7141518B2 (en) | 2003-10-16 | 2006-11-28 | Kimberly-Clark Worldwide, Inc. | Durable charged particle coatings and materials |
US7678367B2 (en) | 2003-10-16 | 2010-03-16 | Kimberly-Clark Worldwide, Inc. | Method for reducing odor using metal-modified particles |
US7754197B2 (en) | 2003-10-16 | 2010-07-13 | Kimberly-Clark Worldwide, Inc. | Method for reducing odor using coordinated polydentate compounds |
US7794737B2 (en) | 2003-10-16 | 2010-09-14 | Kimberly-Clark Worldwide, Inc. | Odor absorbing extrudates |
US7837663B2 (en) | 2003-10-16 | 2010-11-23 | Kimberly-Clark Worldwide, Inc. | Odor controlling article including a visual indicating device for monitoring odor absorption |
US7879350B2 (en) | 2003-10-16 | 2011-02-01 | Kimberly-Clark Worldwide, Inc. | Method for reducing odor using colloidal nanoparticles |
US8211369B2 (en) | 2003-10-16 | 2012-07-03 | Kimberly-Clark Worldwide, Inc. | High surface area material blends for odor reduction, articles utilizing such blends and methods of using same |
US8221328B2 (en) | 2003-10-16 | 2012-07-17 | Kimberly-Clark Worldwide, Inc. | Visual indicating device for bad breath |
US8702618B2 (en) | 2003-10-16 | 2014-04-22 | Kimberly-Clark Worldwide, Inc. | Visual indicating device for bad breath |
US10214858B2 (en) | 2017-04-13 | 2019-02-26 | Rayonier Performance Fibers, Llc | Cellulosic material with antimicrobial and defiberization properties |
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Also Published As
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AU2554088A (en) | 1989-04-18 |
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