|Número de publicación||USRE32476 E|
|Tipo de publicación||Concesión|
|Número de solicitud||US 06/855,001|
|Fecha de publicación||18 Ago 1987|
|Fecha de presentación||22 Abr 1986|
|Fecha de prioridad||21 Dic 1970|
|Número de publicación||06855001, 855001, US RE32476 E, US RE32476E, US-E-RE32476, USRE32476 E, USRE32476E|
|Inventores||John F. Kistner|
|Cesionario original||Minnesota Mining And Manufacturing Company|
|Exportar cita||BiBTeX, EndNote, RefMan|
|Citas de patentes (14), Citada por (22), Clasificaciones (20)|
|Enlaces externos: USPTO, Cesión de USPTO, Espacenet|
Y.sub.1 [(RO).sub.o --Y.sub.2 (NCO).sub.p ].sub.z
This application is a continuation-in-part of my copending application filed Dec. 21, 1970, Ser. No. 100,378, .Badd.now U.S. Pat. No. 4,417,004.Baddend..
This invention relates to stabilization or consolidation of aggregate material. In another aspect, this invention relates to in situ stabilization of superficial or surface-lying aggregate material. In another aspect, this invention relates to consolidation of aggregate material for agricultural purposes to form an integral, water-permeable mass.
Consolidation or stabilization of aggregate materials is generally undertaken to provide a tough, rigid, water-permeable consolidated mass in which some structural strength is inherent. It would be extremely desirable to provide aggregate material with a degree of consolidation while allowing the consolidated mass to retain some of the characteristics of the aggregate material, e.g., water-permeability and the ability to sustain growth of plant life. In order to accomplish this, it is apparent that the consolidated aggregate must be somewhat porous to allow the roots of plant life to obtain oxygen and water vital to sustain growth.
One area where there is a need for the benefits afforded by this invention is in the nursery practice of potting plants or seeds for germination and later transplant. Normally, pots are packed with a growing media such as black dirt, peat moss, etc., which is a time consuming and costly operation. For those nurseries which ship potted plants, substantial freight costs are incurred from the weight of the pots and potting media. Also, the consumer must remove each plant from its pot prior to transplant, again a time-consuming operation.
Another area where a need for the benefits afforded by this invention is apparent is surface area receiving heavy pedestrian traffic such as a playground, backyard play area, or park. These areas usually have bare spots resulting from abrading away of the grass or other cover growth and compaction of the soil inhibiting access of air and water to the roots of said cover growth. Stabilization of such areas to wear and compaction would be desirable but of necessity would require the ability to maintain grass or other cover growth.
Hillsides or sandy slopes or other surface areas which are susceptible to erosion from the action of rain and wind, and on which cover growth is difficult to maintain provide still another area where this invention can be of benefit.
In accordance with the invention there is provided a method for consolidating aggregate materials to form a resilient, integral, water-permeable mass by contacting these materials with a fluid agent comprising a hydrophilic urethane polymer and curing the prepolymer with sufficient water to form a hydrophilic cellular polymer which bonds the aggregate material together.
The novel consolidated material is flexible, resilient, non-compactible, i.e., having a spongy nature, and is hydrophilic and water-permeable (i.e., water will diffuse or permeate through the consolidated mass).
Aggregate material suitable for contacting in accordance with the invention is generally solid particulate matter such as soil (e.g., black dirt, sand), and can include mineral aggregate (e.g., perlite, vermiculite), organic matter (e.g., wood pulp, ground tree bark, sawdust, ground corn cobs, wheat hulls, peat moss), or synthetic aggregate (e.g., ground glass).
The urethane prepolymer or isocyanate-terminated prepolymer useful in this invention is in general a reaction product of a material having a plurality of active hydrogen atoms, such as polyols, with an amount of organic polyisocyanate (or polyisothiocyanate) in excess of stoichiometry. The fluid agent comprising the urethane prepolymer is advantageous in that it is a one-part system, requiring no elaborate equipment for preparation or for application thereof to the aggregate material, with water being the only necessary co-reactant material.
The aggregate material can in general be contacted by physically mixing the fluid agent with the aggregate material to be consolidated and then adding water to the mixture to effect the curing, i.e., polymerizing or cross-linking, reaction. For superficial or surface-lying aggregate, contacting is generally obtained by spraying the aggregate with the prepolymer fluid agent and water to provide a thin, polymeric layer overlying and adhesively bonding to the superficial aggregate.
The urethane prepolymers useful in this invention are known in the art and in general can be prepared by reacting a material having a plurality of active hydrogen atoms, such as polyols, with an amount of organic polyisocyanate (or polyisothiocyanate) in excess of stoichiometry. The equivalent ratio of isocyanate moiety, --NCO, to active hydrogen will be at least 2/1, and preferably at least 2.1/1 to 2.5/1, and can be as high as 4/1 or even higher.
The mechanism of the urethane prepolymer-water reaction is well known; it results in the formation of urea linkages, the water acting as a chain extender, and in the evolution of carbon dioxide which tends to foam the reaction mixture to form a cellular polymer.
One useful class of prepolymers which can be used in this invention are those which are water-miscible and can be expressed in terms of the formula
Y.sub.1 [(RO).sub.o --Y.sub.2 (--NCO).sub.p ].sub.z I
where Y1 is an active hydrogen-free residue of a compound having a plurality of active hydrogen atoms, e.g., polyhydroxy alkane or polyamino alkane such as ethylene glycol or ethylene diamine; (RO)o is a hydrophilic polyoxyalkylene chain having a plurality of oxyethylene units, such as (1) a polyoxyethylene chain (the preferred type of chain), (2) a chain having alternating blocks or backbone segments of oxyethylene and oxypropylene units, or (3) a chain of randomly distributed oxyethylene and oxypropylene units; 0 is the number of oxyalkylene units in the polyoxyalkylene chain; Y2 is a linkage or bridge the function of which is to bond the polyoxyalkylene chain to the isocyanate moieties shown in the formula; p is the number of isocyanate moieties and generally will be 1 to 5, preferably 1 to 3; and z is a number equal to the functionality, or number of this plurality of active-hydrogen atoms, in said compound (e.g., said polyhydroxyalkane or polyaminoalkane) which provides the residue Y1 and generally z will be 2 to 6. Where the prepolymer is prepared by reacting a polyol and a polyisocyanate, the polyoxyalkylane chain will be terminated with --OC(O)NH--R'(--NCO)p, where --OC(O)NH-- is a carbamate (or urethane) group resulting from the reaction of a hydroxyl group from the polyol precursor with an isocyanate moiety from the polyisocyanate precursor, R' is the residue or nucleus of the polyisocyanate precursor (which will be tolylene where the polyisocyanate precursor is tolylene diisocyanate), and p is an integer equal to q-1, where q is the number of isocyanate moieties of the polyisocyanate precursor.
The term "active hydrogen atom" as used herein refers to a hydrogen atom which reacts with the isocyanate moiety under urethane or urea bond forming conditions. The term "water-miscible" in this context means the prepolymer is dispersible (or soluble) in water.
A useful subclass of water-miscible prepolymers within the scope of formula I are those of the formula ##STR1## where Y1, R', o, and z are defined above, R' is tolylene, o is the number of oxyethylene units shown, p is 1 to 3, and z is equal to the functionality, e.g., 2 or 3, of said compound from which Y1 is derived.
Another subclass of water-miscible prepolymers useful in the consolidation of aggregate according to this invention can be expressed by the formula ##STR2## where Y1, R', and z are as defined above in formula II, and a, b, and c are integers such that the ratio of (a+c)/b is greater than 1 (and thus the prepolymers are water-miscible).
Commercially available polyol precursors useful in making the above-described water-miscible isocyanate-terminated prepolymers used in this invention are the hydrophilic poly-(oxyethylene-oxypropylene) polyols sold under the trademark "Pluronic," such as Pluronic L35, F38, and P46, and hydrophilic polyols with heteric oxyethylene-oxypropylene chains sold as "Polyol Functional Fluids," such as WL-580, WL-600, and WL-1400. Generally, the hydrophilic or water-soluble oxyethylene-containing polyols to be used will have molecular weights of at least 200 and as high as 8000; preferably they will have molecular weights of 600 to 2000. Lower molecular weight polymers, i.e., below about 600, are liquids having decreasing solubility in water. When used in this invention they provide decreased hydrophilicity and increased hardness or rigidity and friability to the consolidated aggregate mass. Conversely, higher molecular weight polymers, i.e., greater than about 2000, tend to provide solid prepolymers which require solvation when used in the invention. These also provide increased rigidity or hardness to the consolidated aggregate mass, but are extremely hydrophilic. This increased hydrophilicity causes swelling of the consolidation when saturated with water, affording a wrinkled effect. A preferred polyol (particularly when reacted with tolylene diisocyanate to form the prepolymer) is "Carbowax" 1000, which is a polyethylene glycol having a molecular weight of about 1000.
Polyisocyanates which can be used to prepare the isocyanate-terminated prepolymers used in this invention and described above include conventional aliphatic and aromatic polyisocyanates. The preferred polyisocyanates to be used will be aromatic polyisocyanates because the prepolymers made therefrom will generally react faster with water. One of the most useful polyisocyanate compounds which can be used for this purpose is tolylene diisocyanate, particularly as a blend of 80 weight percent of toluene-2,4-diisocyanate, and 20 weight percent of toluene-2,6-diisocyanate. A 65:35 blend of the 2,4- and 2,6-isomers is also useful. These polyisocyanates are commercially available under the trademark Hylene TM, Nacconate 80, and Mondur TD-80. Other useful polyisocyanate compounds which can be used are other isomers of tolylene diisocyanate, hexamethylene-1,6-diisocyanate, diphenylmethane-4,4'-diisocyanate, m- or p-phenylene diisocyanate, and 1,5-naphthalene diisocyanate. Polymeric polyisocyanates such as polymethylene polyphenyl polyisocyanates can also be used, such as those sold under the trademarks Mondur MRS and PAPI. A list of useful commercially available polyisocyanates is found in "Encyclopedia of Chemical Technology," by Kirk and Othmer, 2nd Ed., Vol. 12, pp. 46-47, Interscience Pub., (1967).
The prepolymers per se used in this invention are generally very viscous liquids and though they can be used by themselves as treating agents, it is preferred to employ the same in the form of a solution in a suitable solvent which is non-reactive with the isocyanate moiety. Thus, organic solvents, or other organic compounds which contain active hydrogen atoms are to be avoided in making up and using the prepolymer agents of this invention. Generally these solvents can be water-miscible polar organic solvents, preferably volatile at ambient conditions. Alternatively, the solvent can be a water-immiscible organic solvent which volatilizes under ambient conditions and escapes to the atmosphere from the treated mass of aggregate. Representative solvents which can be used include acetone, tetrahydrofuran, methyl ethyl ketone, methylene chloride, toluene, and methoxyethylacetate. Water itself can be used as a solvent though the resulting solution will have to be applied to the aggregate before the curing of the prepolymer takes place. By controlling the temperature of the aqueous solution, the hiatus between making up the aqueous solution and its application to the aggregate can be varied; the lower the temperature, the longer the pot-life of the solution. The concentration of the prepolymer in the solvent can vary, depending upon such factors as the viscosity desired, the technique of treating the aggregate, and the amount of materials such as grass and fertilizer contained in the solution. Generally concentrations of 5 to 90 weight percent, will be suitable.
While effective consolidation of the aggregate can be realized without the use of a surfactant, it is preferable to include a small amount of a surfactant in the prepolymer solution. The use of a surfactant is desirable because it enhances the stability of the cell structure of the polymeric matrix during cure and insures complete wetting of the aggregate particles by the prepolymer agent. Suitable surfactants are known to the art and include polyoxyethylene derivatives of alkyl- and aryl-hydroxy and -carboxy compounds as well as sulfonated alkyl and aryl compounds, fatty acid soaps, e.g., calcium octoate, and fluorocarbon surfactants. A preferred surfactant is a polyoxyethylene derivative of fatty acid partial esters of hexatol anhydrides, available commercially from the Atlas Powder Company under the trade name designation "Tween 80." An additional commercial surfactant suitable for the use in this invention includes "Silicone Oil 120" available from Dow Chemical Co. If a surfactant is utilized, its concentration should be in the range of 1 to 2 weight percent of the prepolymer. Concentrations above this range, while not detrimental, provide no additional benefit.
The aggregate material for which the invention is useful is in general unconsolidated or loose particulate matter such as soil (e.g., black dirt, sand), including superficial soil, mineral aggregate (e.g., perlite, vermiculite), organic matter (e.g., wood pulp, ground tree bark, sawdust, ground corn cobs, wheat hulls, peat moss), synthetic aggregate (e.g., ground glass), or mixtures of the same.
The manner of contacting the aggregate material to form an integral water-permeable mass can vary depending on the intended use for the consolidated mass. For example, if the aggregate is to be consolidated in such a manner as to provide a potting compound for seeds or seedlings, the prepolymer agent is merely inter-mixed with the aggregate (which is preferably moisture-free), together with desired fertilizer, herbicides, etc., followed by mixing with water to yield a pourable slurry. This slurry can then be cast into a reuseable mold of desired configuration until cured, at which time the mold can be removed yielding a cohesive, hydrophilic, consolidated mass which retains the mold configuration.
Seeds can be inserted in the consolidated mass by making a small slit or hole in the surface of the mass with a knife, pencil, or similar object, and merely placing the seed in the opening. Alternately, the seeds can be placed on the surface of the consolidated mass and covered lightly with a layer of agricultural media such as black dirt until germination, much the same as present nursery practice. Seedlings can be inserted in a hole in the consolidated mass made by pencil or similarly shaped object.
When consolidating aggregate material for use in potting plants, etc., as just described, it is preferable to dry the aggregate prior to contacting it with the prepolymer so that it has a free-flowing consistency without clumps or lumps. This will insure adequate contact of aggregate surface area by the prepolymer agent with a minimum of agitation of the mixture prior to curing.
Where a thin layer of aggregate is desired to be consolidated in situ, as on a sandy slope or hillside to reduce erosion, a spray application of the prepolymer can be utilized. Concentration of prepolymer in a sprayable solvent composition should be on the order of about 50 to 75 percent, although lesser concentrations may be desirable when the composition includes grass seed, fertilizer, etc. in amounts which would increase the viscosity of the composition. Sprayable compositions containing 50-75 percent prepolymer are generally applied at the rate of approximately 1/2 to 2 gallons per 100 square feet of superficial aggregate. Spray equipment useful for applying such compositions is preferably a dual hose arrangement whereby water is delivered from one source and the prepolymer agent from a separate source, with mixing of the prepolymer and water occurring in a common spray nozzle or occurring by the individual spray streams impinging on one another. The water can also be sprayed separately after the prepolymer coating has been applied to the superficial aggregate, with satisfactory results. The polymer may be sprayed by utilizing a commercial hydroseeder or hydromulcher, followed by a water spray.
The amount of water required to effect a cure with the prepolymer should be that sufficient to yield a water-insoluble, solid, cellular polymer matrix in which the aggregate is bonded. Normally the weight ratio of water to prepolymer will be in the range of 0.1:1 to 20:1. When consolidating aggregate material to provide a potting compound, a ratio of 1:1 to 5:1 is preferred, and when consolidating superficial aggregate in situ a ratio of 3:1 to 15:1 is preferred.
The amount of prepolymer required to consolidate the aggregate material will in general be in the range of about 1 to 40 weight percent, or higher, and preferably 3 to 20 weight percent, based on the weight of the aggregate material. When utilizing the preferred polyol of about 1000 molecular weight, lower concentrations of prepolymer, i.e., below 3 weight percent of the aggregate, provide greater porosity and dimensional stability (i.e., the cured mass will not swell when saturated with water), and afford less resiliency and strength to the cured mass. Increasing concentrations tend to increase resiliency and compression and tensile strength while decreasing porosity and dimensional stability.
The prepolymer can be cured under atmospheric conditions in hot or cold weather to provide a cellular polymeric matrix which provides a flexible, non-compactible, somewhat spongy, hydrophilic, water-permeable mass of aggregate which has the appearance of the initial aggregate. Since the cured mass is water-permeable, water will diffuse through or permeate the mass. The hydrophilicity of the polymer making up the cell walls of the consolidation allows water to be retained by the mass, and the cellular nature allows "breathing" of the consolidated mass. The density of the consolidated mass is reduced from that of the unconsolidated aggregate, thereby affording a nursery man who ships potted plants or seedlings a substantial reduction in shipping costs.
Objects and advantages of this invention are illustrated in the following examples, but the various materials and amounts thereof and various other conditions and details recited therein should not be construed to unduly limit this invention.
One-thousand parts by weight of polyoxyethylene diol (Carbowax 1000, having a molecular weight of about 1000) was stirred and reacted with 351 parts of tolylene diisocyanate (80/20 mixture of the 2,4- and 2,6-isomers) under substantially anhydrous conditions for about 2 hrs., and the reaction mixture was allowed to stand for several days. The resulting urethane prepolymer was a viscous liquid (at 25° C.) having a structure in accordance with formula II, where Y1 is the residue of ethylene glycol, R' is tolylene, o is about 21, p is 1, and z is 2.
A potting media was prepared by intimately mixing 20 parts of the prepolymer of Example 1 (in a 90 percent solids solution with acetone) with 291 parts of free-flowing sand (sp. gr. 1.7), adding 60 parts water to the resulting mixture and stirring vigorously with a spatula for about 20 seconds. The stirred mixture cured in about 10 minutes at room temperature to provide an integral, resilient (even when very wet), non-friable, porous, water-permeable consolidated structure.
The density of the cured system was 43 percent less than the sand itself. Germination and growth of tomatoes, cucumbers, beans, flowers (e.g., African Violets, Begonias), and jack pine seedlings progressed in the cured polymeric mass.
A potting media was prepared utilizing the following components:
______________________________________ Specific Gravity Wt., gms.______________________________________Peat Moss - 1/3 by volume)Vermiculite - 1/3 by volume) 0.65 260Sand - 1/3 by volume)prepolymer solution of Ex. 2 1.1 40acetone 0.8 24water 1.0 150After Cure 0.37 474______________________________________
The prepolymer, acetone, and water were rapidly mixed together, poured onto the physically mixed aggregate, and the entire mixture was then vigorously stirred for 30 seconds with a spatula. After 10 minutes at room temperature, the stirred mixture was cured to a porous, resilient, non-friable, water-permeable, consolidated structure. The density of the consolidated structure was 43 percent less than the initial aggregate material mixture. This consolidated structure is useful for growing the same products illustrated in Example 1.
A 30 sq. ft. plot of superficial soil was raked and smoothed and then sprinkled with one gallon of a 33 wt. percent acetone solution of the prepolymer of Example 1. Immediately thereafter, grass seed was uniformly spread over the treated soil in the amount of 2-5 pounds/1000 ft2 and raked into the treated soil to a depth of 1-2". The treated soil was immediately watered lightly. The prepolymer consolidated the soil in about 10-20 min. to a resilient mass which readily soaked up water. A laboratory test, run in a similar manner, using rye grass seed, resulted in a higher rate of germination of the seed than was obtained with seed planted in untreated soil.
A sandy hillside was sprayed with a 50 weight percent acetone solution of the prepolymer of Example 1 utilizing low pressure spray equipment to provide 36 gm. of active prepolymer per square foot of contact surface. This area was then raked with a common garden rake and sprinkled with grass seed. Approximately 20 minutes later the contacted area was sprayed with water from a common garden hose until the area was saturated and runoff began to occur. Within 15 to 20 minutes the prepolymer cured and consolidated the soil to a resilient, water-permeable mass. A control area adjacent to the treated area was raked and seeded at the same time. Eleven months later the treated area showed no signs of erosion, and the grass seed germinated. The control area had rivulets or channels 11/2 to 2 inches deep through it due to erosion, and most of the grass seed was washed away.
An aluminum tray, approximately 9×13 inches and one inch deep was filled with sand. 20 grams of the prepolymer solution described in Example 2 was mixed with 250 ml. water and immediately sprinkled evenly over the surface of the sand. After 15 minutes, the tray was tilted at a 45° angle and flushed with a strong stream of water from a water faucet. No sand was washed away from the tray by the water. A resilient skin bonding the sand particles into an integral covering prevented erosion of the sand in the tray. The same results were obtained when 20 g. of the prepolymer solution was mixed with 60 ml., 100 ml., 150 ml., 200 ml., and 300 ml., of water.
Modifications and variations of this invention will become apparent to those skilled in the art without departing from the scope of this invention, and this invention is not to be unduly limited to the illustrative embodiments set forth herein.
|Patente citada||Fecha de presentación||Fecha de publicación||Solicitante||Título|
|US2867278 *||16 Nov 1956||6 Ene 1959||Great Western Drilling Company||Sealing porous formations|
|US3181611 *||29 Jun 1961||4 May 1965||Dow Chemical Co||Selective prevention of water and brine intrusion into mineral producing strata|
|US3354099 *||10 Mar 1964||21 Nov 1967||Frederick C Stegeman||Polyurethane-hydraulic cement compositions and process for manufacturing the same|
|US3367892 *||28 Sep 1966||6 Feb 1968||Thiokol Chemical Corp||Polymeric soil-stabilizing compositions and method of using the same|
|US3373009 *||30 Jul 1964||12 Mar 1968||Dow Chemical Co||Nutrient plant matrix|
|US3401128 *||8 Feb 1965||10 Sep 1968||Hoover Ball & Bearing Co||Polyurethane foam product and method of making same|
|US3409579 *||2 May 1967||5 Nov 1968||Ashland Oil Inc||Foundry binder composition comprising benzylic ether resin, polyisocyanate, and tertiary amine|
|US3441523 *||12 Nov 1964||29 Abr 1969||Allied Chem||Filled cellular urethanes|
|US3463745 *||29 Dic 1966||26 Ago 1969||Olin Mathieson||Polyurethane sponge and process therefor|
|US3472644 *||26 May 1965||14 Oct 1969||Mrs Charles A Zamzov||Foamed synthetic polymeric plant growth medium containing an inorganic filler and microorganisms|
|US3538020 *||23 Sep 1966||3 Nov 1970||Kata Mfg & Filtering Co The||Fluid purification device containing a cartridge of polymer entrapped aggregate particles|
|US3651649 *||26 Ago 1970||28 Mar 1972||Dow Chemical Co||Stabilization of soil with water-in-vinyl ester resin emulsions|
|US3706678 *||3 Ago 1970||19 Dic 1972||Bayer Ag||Hydrophilic polyurethane foams prepared from biuret containing polyisocyanates|
|US3719050 *||1 Jun 1970||6 Mar 1973||Toho Chem Ind Co Ltd||Soil stabilization method|
|Patente citante||Fecha de presentación||Fecha de publicación||Solicitante||Título|
|US5064653 *||29 Mar 1988||12 Nov 1991||Ferris Mfg. Co.||Hydrophilic foam compositions|
|US6479433||2 Oct 2000||12 Nov 2002||Smithers-Oasis Company||Polyurethane foam composites for grower applications and related methods|
|US6572809 *||23 Abr 1999||3 Jun 2003||Agritecno Yazaki Co., Ltd.||Gel coating method and apparatus|
|US8261486||16 Ene 2007||11 Sep 2012||Aerogrow International, Inc.||Systems and methods for controlling liquid delivery and distribution to plants|
|US8595974 *||9 Mar 2007||3 Dic 2013||George Pierce Nottingham||Agricultural polymer protected root ball|
|US8677687||9 Oct 2013||25 Mar 2014||George Pierce Nottingham||Method of producing an agricultural polymer protected root ball|
|US8701344 *||18 Jun 2004||22 Abr 2014||Suntory Holdings Limitied||Plant cultivating substrate and method of its manufacture|
|US8916668 *||7 Jun 2011||23 Dic 2014||Biopolymer Technologies, Ltd.||Protein-containing adhesives, and manufacture and use thereof|
|US9309444||26 Jul 2013||12 Abr 2016||Biopolymer Technologies, Ltd.||Protein-containing emulsions and adhesives, and manufacture and use thereof|
|US9416303||25 Nov 2014||16 Ago 2016||Biopolymer Technologies, Ltd.||Protein-containing adhesives, and manufacture and use thereof|
|US20050102895 *||17 Nov 2003||19 May 2005||W. Michael Bissonnette||Soil-less seed support medium and method for germinating a seed|
|US20050257424 *||22 Abr 2005||24 Nov 2005||Aerogrow International, Inc.||Devices and methods for growing plants|
|US20060179711 *||15 Sep 2004||17 Ago 2006||Aerogrow International, Inc.||Devices and methods for growing plants|
|US20060248796 *||18 Jun 2004||9 Nov 2006||Masaki Hashimoto||Plant cultivating base body and method of manufacturing the same|
|US20060272210 *||19 Jun 2006||7 Dic 2006||Aerogrow International, Inc.||Smart garden devices and methods for growing plants|
|US20070271841 *||12 Ene 2007||29 Nov 2007||Aerogrow International, Inc.||Devices and methods for growing plants|
|US20070271842 *||16 Ene 2007||29 Nov 2007||Aerogrow International, Inc.||Systems and methods for controlling liquid delivery and distribution to plants|
|US20080120907 *||9 Mar 2007||29 May 2008||George Pierce Nottingham||Agricultural Polymer Protected Root Ball|
|US20080222949 *||12 Mar 2008||18 Sep 2008||Aerogrow International, Inc.||Devices and methods for growing plants|
|US20080282610 *||12 Mar 2008||20 Nov 2008||Aerogrow International, Inc.||Devices and methods for growing plants|
|US20100278594 *||30 Abr 2009||4 Nov 2010||Geostorage Corporation||Erosion control system|
|US20110311833 *||7 Jun 2011||22 Dic 2011||Parker Anthony A||Protein-Containing Adhesives, and Manufacture and Use Thereof|
|Clasificación de EE.UU.||405/264, 521/99, 47/58.10R, 521/905|
|Clasificación internacional||C08G18/48, C08G18/10, E02B3/16, A01G9/10, C09K17/30|
|Clasificación cooperativa||A01G9/1086, C09K17/30, C08G18/4833, C08G2310/00, E02B3/16, C08G18/10|
|Clasificación europea||C08G18/10, C08G18/48F, E02B3/16, C09K17/30, A01G9/10K|