The invention relates to texturized cellulosic or lignocellulosic materials and compositions and composites made from such texturized materials.
Cellulosic and lignocellulosic materials are produced, processed, and used in large quantities in a number of applications. Once used, these materials are usually discarded. As a result, there is an ever-increasing amount of waste cellulosic and lignocellulosic material.
In general, the invention features texturized cellulosic or lignocellulosic materials and compositions and composites made therefrom.
In one embodiment, the invention features a process for preparing a texturized fibrous material. The process involves shearing a cellulosic or lignocellulosic material having internal fibers (e.g., flax; hemp; cotton; jute; rags; finished or unfinished paper, paper products, including poly-coated paper, or byproducts of paper manufacturing such as pulp board; or synthetic cellulosic or lignocellulosic materials such as rayon), to the extent that the internal fibers are substantially exposed, resulting in texturized fibrous material. The cellulosic or lignocellulosic material can be a woven material such as a woven fabric, or a non-woven material such as paper or bathroom tissue. The exposed fibers of the texturized fibrous material can have a length/diameter (L/D) ratio of at least about 5 (at least about 5, 10, 25, 50, or more). For example, at least about 50% of the fibers can have L/D ratios of this magnitude.
In another embodiment, the invention features a texturized fibrous material that includes a cellulosic or lignocellulosic material having internal fibers, where the cellulosic or lignocellulosic material is sheared to the extent that the internal fibers are substantially exposed.
The texturized fibrous material can, for example, be incorporated into (e.g., associated with, blended with, adjacent to, surrounded by, or within) a structure or carrier (e.g., a netting, a membrane, a flotation device, a bag, a shell, or a biodegradable substance). Optionally, the structure or carrier may itself be made from a texturized fibrous material (e.g., a texturized fibrous material of the invention), or of a composition or composite of a texturized fibrous material.
The texturized fibrous material can have a bulk density less than about 0.5 grams per cubic centimeter, or even less than about 0.2 g/cm3.
Compositions that include the texturized fibrous materials described above, together with a chemical or chemical formulation (e.g., a pharmaceutical such as an antibiotic or contraceptive, optionally with an excipient; an agricultural compound such as a fertilizer, herbicide, or pesticide; or a formulation that includes enzymes) are also within the scope of the invention, as are compositions that include the texturized fibrous materials and other liquid or solid ingredients (e.g., particulate, powdered, or granulated solids such as plant seed, foodstuffs, or bacteria).
Composites that include thermoplastic resin and the texturized fibrous materials are also contemplated. The resin can be, for example, polyethylene, polypropylene, polystyrene, polycarbonate, polybutylene, a thermoplastic polyester, a polyether, a thermoplastic polyurethane, polyvinylchloride, or a polyamide, or a combination of two or more resins.
In some cases, at least about 5% by weight (e.g., 5%, 10%, 25%, 50%, 75%, 90%, 95%, 99%, or about 100%) of the fibrous material included in the composites is texturized.
The composite may include, for example, about 30% to about 70% by weight resin and about 30% to about 70% by weight texturized fibrous material, although proportions outside of these ranges may also be used. The composites can be quite strong, in some cases having a flexural strength of at least about 6,000 to 10,000 psi.
In another embodiment, the invention features a composite including a resin, such as a thermoplastic resin, and at least about 2% by weight, more preferably at least about 5% by weight, texturized cellulosic or lignocellulosic fiber. The invention also features a composite that includes polyethylene and at least about 50% by weight texturized cellulosic or lignocellulosic fiber.
The invention further features composites, including a resin and cellulosic or lignocellulosic fiber, that have flexural strengths of at least about 3,000 psi, or tensile strengths of at least about 3,000 psi.
In addition, the invention features a process for manufacturing a composite; the process includes shearing cellulosic or lignocellulosic fiber to form texturized cellulosic or lignocellulosic fiber, then combining the texturized fiber with a resin. A preferred method includes shearing the fiber with a rotary knife cutter. The invention also features a process for manufacturing a composite that includes shearing cellulosic or lignocellulosic fiber and combining the fiber with a resin.
The composites can also include inorganic additives such as calcium carbonate, graphite, asbestos, wollastonite, mica, glass, fiber glass, chalk, talc, silica, ceramic, ground construction waste, tire rubber powder, carbon fibers, or metal fibers (e.g., stainless steel or aluminum). The inorganic additives can represent about 0.5% to about 20% of the total weight of the composite.
The composite can be in the form of, for example, a pallet (e.g., an injection molded pallet), pipes, panels, decking materials, boards, housings, sheets, poles, straps, fencing, members, doors, shutters, awnings, shades, signs, frames, window casings, backboards, wallboards, flooring, tiles, railroad ties, forms, trays, tool handles, stalls, bedding, dispensers, staves, films, wraps, totes, barrels, boxes, packing materials, baskets, straps, slips, racks, casings, binders, dividers, walls, indoor and outdoor carpets, rugs, wovens, and mats, frames, bookcases, sculptures, chairs, tables, desks, art, toys, games, wharves, piers, boats, masts, pollution control products, septic tanks, automotive panels, substrates, computer housings, above- and below-ground electrical casings, furniture, picnic tables, tents, playgrounds, benches, shelters, sporting goods, beds, bedpans, thread, filament, cloth, plaques, trays, hangers, servers, pools, insulation, caskets, bookcovers, clothes, canes, crutches, and other construction, agricultural, material handling, transportation, automotive, industrial, environmental, naval, electrical, electronic, recreational, medical, textile, and consumer products. The composites can also be in the form of a fiber, filament, or film.
The terms “texturized cellulosic or lignocellulosic material” and “texturized fibrous material” as used herein, mean that the cellulosic or lignocellulosic material has been sheared to the extent that its internal fibers are substantially exposed. At least about 50%, more preferably at least about 70%, of these fibers have a length/diameter (L/D) ratio of at least 5, more preferably at least 25, or at least 50. An example of texturized cellulosic material is shown in
The texturized fibrous materials of the invention have properties that render them useful for various applications. For example, the texturized fibrous materials have absorbent properties, which can be exploited, for example, for pollution control. The fibers are generally biodegradable, making them suitable, for example, for drug or chemical delivery (e.g., in the treatment of humans, animals, or in agricultural applications). The texturized fibrous materials can also be used to reinforce polymeric resins.
Those composites that include texturized fibrous material and resin are strong, lightweight, and inexpensive. The raw materials used to make the composites are available as virgin or recycled materials; for example, they may include discarded containers composed of resins, and waste cellulosic or lignocellulosic fiber.
Other features and advantages of the invention will be apparent from the following detailed description, and from the claims.
Examples of cellulosic raw materials include paper and paper products such as newsprint, poly-coated paper, and effluent from paper manufacture; examples of lignocellulosic raw materials include wood, wood fibers, and wood-related materials, as well as materials derived from kenaf, grasses, rice hulls, bagasse, cotton, jute, other stem plants (e.g., hemp, flax, bamboo; both bast and core fibers), leaf plants (e.g., sisal, abaca), and agricultural fibers (e.g., cereal straw, corn cobs, rice hulls, and coconut hair). Aside from virgin raw materials, post-consumer, industrial (e.g., offal), and processing waste (e.g., effluent) can also be used as fiber sources.
Preparation of Texturized Fibrous Material
If scrap cellulosic or lignocellulosic materials are used, they should be clean and dry. The raw material can be texturized using any one of a number of mechanical means, or combinations thereof. One method of texturizing includes first cutting the cellulosic or lignocellulosic material into ¼- to ½-inch pieces, if necessary, using a standard cutting apparatus. Counter-rotating screw shredders and segmented rotating screw shredders such as those manufactured by Munson (Utica, N.Y.) can also be used, as can a standard document shredder as found in many offices.
The cellulosic or lignocellulosic material is then sheared with a rotary cutter, such as the one manufactured by Sprout, Waldron Companies, as described in Perry's Chem. Eng. Handbook, 6th Ed., at 8–29 (1984). Although other settings can be used, the spacing between the rotating knives and bed knives of the rotary cutter is typically set to 0.020″ or less, and blade rotation is set to 750 rpm or more. The rotary cutter can be cooled to 100° C. or lower during the process, for example, using a water jacket.
The texturized material is passed through a discharge screen. Larger screens (e.g., up to 6 mm) can be used in large-scale production. The cellulosic or lignocellulosic feedstock is generally kept in contact with the blades of the rotary cutter until the fibers are pulled apart; smaller screens (e.g., 2 mm mesh) provide longer residence times and more complete texturization, but can result in lower length/diameter (L/D) aspect ratios. A vacuum drawer can be attached to the screen to maximize and maintain fiber length/diameter aspect ratio.
The texturized fibrous materials can be directly stored in sealed bags or may be dried at approximately 105° C. for 4–18 hours (e.g., until the moisture content is less than about 0.5%) immediately before use.
Alternative texturizing methods include stone grinding, mechanical ripping or tearing, and other methods whereby the material's internal fibers can be exposed (e.g., pin grinding, air attrition milling).
Uses of Texturized Fibrous Material
Texturized fibrous materials and compositions and composites of such fibers with other chemicals and chemical formulations can be prepared to take advantage of the material's properties. The materials can be used to absorb chemicals, for example, potentially absorbing many times their own weight. Thus, the materials could, for instance, be used to absorb spilled oil, or for clean-up of environmental pollution, for example, in water, in the air, or on land. Similarly, the material's absorbent properties, together with its biodegradability, also make them useful for delivery of chemicals or chemical formulations. For example, the materials can be treated with solutions of enzymes or pharmaceuticals such as antibiotics, nutrients, or contraceptives, and any necessary excipients, for drug delivery (e.g., for treatment of humans or animals, or for use as or in animal feed and/or bedding), as well as with solutions of fertilizers, herbicides, or pesticides. The materials can optionally be chemically treated to enhance a specific absorption property. For example, the materials can be treated with silanes to render them lipophilic.
Compositions including texturized materials combined with liquids or particulate, powdered, or granulated solids can also be prepared. For example, texturized materials can be blended with seeds (i.e., with or without treatment with a solution of fertilizer, pesticides, etc.), foodstuffs, or bacteria (e.g., bacteria that digest toxins). The ratio of fibrous materials to the other components of the compositions will depend on the nature of the components and readily be adjusted for a specific product application.
In some cases, it may be advantageous to associate the texturized fibrous materials, or compositions or composites of such materials, with a structure or carrier such as a netting, a membrane, a flotation device, a bag, a shell, or a biodegradable substance. Optionally, the structure of carrier may itself be made of a texturized fibrous material (e.g., a material of the invention), or a composition or composite thereof.
Composites of Texturized Fibrous Material and Resin
Texturized fibrous materials can also be combined with resins to form strong, lightweight composites. Materials that have been treated with chemicals or chemical formulations, as described above, can similarly be combined with biodegradable or non-biodegradable resins to form composites, allowing the introduction of, for example, hydrophilic substances into otherwise hydrophobic polymer matrices. Alternatively, the composites including texturized fibrous materials and resin can be treated with chemicals or chemical formulations.
The texturized cellulosic or lignocellulosic material provides the composite with strength. The composite may include from about 10% to about 90%, for example from about 30% to about 70%, of the texturized cellulosic or lignocellulosic material by weight.
The resin encapsulates the texturized cellulosic or lignocellulosic material in the composites, and helps control the shape of the composites. The resin also transfers external loads to the fibrous materials and protects the fiber from environmental and structural damage. Composites can include, for example, about 10% to about 90%, more preferably about 30% to about 70%, by weight, of the resin.
Resins are used in a variety of applications, for example, in food packaging. Food containers made of resins are typically used once, then discarded. Examples of resins that are suitably combined with texturized fibers include polyethylene (including, e.g., low density polyethylene and high density polyethylene), polypropylene, polystyrene, polycarbonate, polybutylene, thermoplastic polyesters (e.g., PET), polyethers, thermoplastic polyurethane, PVC, polyamides (e.g., nylon) and other resins. It is preferred that the resins have a low melt flow index. Preferred resins include polyethylene and polypropylene with melt flow indices of less than 3 g/10 min, and more preferably less than 1 g/10 min.
The resins can be purchased as virgin material, or obtained as waste materials, and can be purchased in pelletized or granulated form. One source of waste resin is used polyethylene milk bottles. If surface moisture is present on the pelletized or granulated resin, however, it should be dried before use.
The composites can also include coupling agents. The coupling agents help to bond the hydrophilic fibers to the hydrophobic resins. Examples of coupling agents include maleic anhydride modified polyethylenes, such those in the FUSABOND® (available from DuPont, Delaware) and POLYBOND® (available from Uniroyal Chemical, Connecticut) series. One suitable coupling agent is a maleic anhydride modified high density polyethylene such as FUSABOND® MB 100D.
The composites can also contain additives known to those in the art of compounding, such as plasticizers, lubricants, antioxidants, opacificers, heat stabilizers, colorants, flame retardants, biocides, impact modifiers, photostabilizers, and antistatic agents.
The composites can also include inorganic additives such as calcium carbonate, graphite, asbestos, wollastonite, mica, glass, fiber glass, chalk, silica, talc, ceramic, ground construction waste, tire rubber powder, carbon fibers, or metal fibers (e.g., aluminum, stainless steel). When such additives are included, they are typically present in quantities of from about 0.5% up to about 20–30% by weight. For example, submicron calcium carbonate can be added to the composites of fiber and resin to improve impact modification characteristics or to enhance composite strength.
Preparation of Compositions
Compositions containing the texturized cellulosic or lignocellulosic materials and chemicals, chemical formulations, or other solids can be prepared, for example, in various immersion, spraying, or blending apparatuses, including, but not limited to, ribbon blenders, cone blenders, double cone blenders, and Patterson-Kelly “V” blenders.
For example, a composition containing 90% by weight texturized cellulosic or lignocellulosic material and 10% by weight ammonium phosphate or sodium bicarbonate can be prepared in a cone blender to create a fire-retardant material for absorbing oil.
Preparation of Composites of Texturized Fiber and Resin
Composites of texturized fibrous material and resin can be prepared as follows. A standard rubber/plastic compounding 2-roll mill is heated to 325–400° F. The resin (usually in the form of pellets or granules) is added to the heated roll mill. After about 5 to 10 minutes, the coupling agent is added to the roll mill. After another five minutes, the texturized cellulosic or lignocellulosic material is added to the molten resin/coupling agent mixture. The texturized material is added over a period of about 10 minutes.
The composite is removed from the roll mill, cut into sheets and allowed to cool to room temperature. It is then compression molded into plaques using standard compression molding techniques.
Alternatively, a mixer, such as a Banbury internal mixer, is charged with the ingredients. The ingredients are mixed, while the temperature is maintained at less than about 190° C. The mixture can then be compression molded.
In another embodiment, the ingredients can be mixed in an extruder mixer, such as a twin-screw extruder equipped with co-rotating screws. The resin and the coupling agent are introduced at the extruder feed throat; the texturized cellulosic or lignocellulosic material is introduced about ⅓ of the way down the length of the extruder into the molten resin. The internal temperature of the extruder is maintained at less than about 190° C. At the output, the composite can be, for example, pelletized by cold strand cutting.
Alternatively, the mixture can first be prepared in a mixer, then transferred to an extruder.
In another embodiment, the composite can be formed into fibers, using fiber-forming techniques known to those in the art, or into filaments for knitting, warping, weaving, braiding, or making non-wovens. In a further embodiment, the composite can be made into a film.
Properties of the Composites of Texturized Fibrous Material and Resin
The resulting composites include a network of fibers, encapsulated within a resin matrix. The fibers form a lattice network, which provides the composite with strength. Since the cellulosic or lignocellulosic material is texturized, the amount of surface area available to bond to the resin is increased, in comparison to composites prepared with un-texturized cellulosic or lignocellulosic material. The resin binds to the surfaces of the exposed fibers, creating an intimate blend of the fiber network and the resin matrix. The intimate blending of the fibers and the resin matrix further strengthens the composites.
Uses of the Composites of Texturized Fibrous Material and Resin
The resin/fibrous material composites can be used in a number of applications. The composites are strong and light weight; they can be used, for example, as wood substitutes. The resin coating renders the composites water-resistant, so they may be used in outdoor applications. For example, the composites may be used to make pallets, which are often stored outdoors for extended periods of time, wine staves, rowboats, furniture, skis, and oars. Many other uses are contemplated, including panels, pipes, decking materials, boards, housings, sheets, poles, straps, fencing, members, doors, shutters, awnings, shades, signs, frames, window casings, backboards, wallboards, flooring, tiles, railroad ties, forms, trays, tool handles, stalls, bedding, dispensers, staves, films, wraps, totes, barrels, boxes, packing materials, baskets, straps, slips, racks, casings, binders, dividers, walls, indoor and outdoor carpets, rugs, wovens, and mats, frames, bookcases, sculptures, chairs, tables, desks, art, toys, games, wharves, piers, boats, masts, pollution control products, septic tanks, automotive panels, substrates, computer housings, above- and below-ground electrical casings, furniture, picnic tables, tents, playgrounds, benches, shelters, sporting goods, beds, bedpans, thread, filament, cloth, plaques, trays, hangers, servers, pools, insulation, caskets, bookcovers, clothes, canes, crutches, and other construction, agricultural, material handling, transportation, automotive, industrial, environmental, naval, electrical, electronic, recreational, medical, textile, and consumer products. Numerous other applications are also envisioned. The composites may also be used, for example, as the base or carcass for a veneer product. Moreover, the composites can be, for example, surface treated, grooved, milled, shaped, imprinted, textured, compressed, punched, or colored. The surface of the composites can be smooth or rough.
The following examples illustrate certain embodiments and aspects of the present invention and not to be construed as limiting the scope thereof.
A 1500 pound skid of virgin, half-gallon juice cartons made of polycoated white kraft board was obtained from International Paper. Each carton was folded flat.
The cartons were fed into a 3 hp Flinch Baugh shredder at a rate of approximately 15 to 20 pounds per hour. The shredder was equipped with two rotary blades, each 12″ in length, two fixed blades, and a 0.3″ discharge screen. The gap between the rotary and fixed blades was 0.10″.
The output from the shredder, consisting primarily of confetti-like pieces, about 0.1″ to 0.5″ in width and about 0.25″ to 1″ in length, was then fed into a Thomas Wiley Mill Model 2D5 rotary cutter. The rotary cutter had four rotary blades, four fixed blades, and a 2 mm discharge screen. Each blade was approximately 2″ long. The blade gap was set at 0.020″.
The rotary cutter sheared the confetti-like pieces across the knife edges, tearing the pieces apart and releasing a finely texturized fiber at a rate of about one pound per hour. The fiber had an average minimum L/D ratio of between five and 100 or more. The bulk density of the texturized fiber was on the order of 0.1 g/cc.
Composites of texturized fiber and resin were prepared as follows. A standard rubber/plastic compounding 2-roll mill was heated to 325–400° F. The resin (usually in the form of pellets or granules) was added to the heated roll mill. After about 5 to 10 minutes, the resin banded on the rolls (i.e., it melted and fused on the rolls). The coupling agent was then added to the roll mill. After another five minutes, the texturized cellulosic or lignocellulosic material was added to the molten resin/coupling agent mixture. The cellulosic or lignocellulosic fiber was added over a period of about 10 minutes.
The composite was then removed from the roll mill, cut into sheets, and allowed to cool to room temperature. Batches of about 80 g each were compression molded into 6″×6″×⅛″ plaques using standard compression molding techniques.
One composition contained the following ingredients:
1Marlex 16007
2Texturized using rotary cutter with 2 mm mesh
3FUSABOND ® 100D
The plaques were machined into appropriate test specimens and tested according to the procedures outlined in the method specified. Three different specimens were tested for each property, and the mean value for each test was calculated. The properties of Composition No. 1 are as follows:
A second composition contains the following ingredients:
The properties of Composition No. 2 are as follows:
A third composition contains the following ingredients:
The properties of Composition No. 3 are as follows:
A fourth composition contains the following ingredients:
4Virgin polycoated milk cartons
The properties of Composition No. 4 are as follows:
A fifth composition contains the following ingredients:
The properties of Composition No. 5 are as follows:
A sixth composition contains the following ingredients:
The properties of Composition No. 6 are as follows:
A seventh composition contains the following ingredients:
5HDPE with melt-flow index <1
The properties of Composition No. 7 are as follows:
other embodiments are within the claims.
This application is a divisional of U.S. patent application Ser. No. 09/772,593, filed Jan. 30, 2001, which is a continuation-in-part of U.S. patent application Ser. No. 09/337,580, filed Jun. 22, 1999 now U.S. Pat. No. 6,207,729, which is a continuation in part of U.S. patent application Ser. No. 08/961,863, filed Oct. 31, 1997, now issued as U.S. Pat. No. 5,973,035; is a continuation-in-part of U.S. patent application Ser. No. 09/338,209, filed Jun. 22, 1999 now abandoned, which is a continuation-in-part of U.S. patent application Ser. No. 08/921,807, filed Sep. 2, 1997, now issued as U.S. Pat. No. 5,952,105; and is a continuation in part of U.S. patent application Ser. No. 09/290,031, filed Apr. 9, 1999 now U.S. Pat. No. 6,258,876, hereby incorporated by reference.
Number | Name | Date | Kind |
---|---|---|---|
1824221 | Mason | Sep 1931 | A |
2516847 | Boehm | Aug 1950 | A |
2519442 | Delorme et al. | Aug 1950 | A |
2558378 | Petry | Jun 1951 | A |
2635976 | Meiler et al. | Apr 1953 | A |
2658828 | Pattilloch | Nov 1953 | A |
2665261 | Baker | Jan 1954 | A |
2680102 | Becher | Jun 1954 | A |
2757150 | Heritage | Jul 1956 | A |
2789903 | Lukman et al. | Apr 1957 | A |
2935763 | Newman et al. | May 1960 | A |
3308218 | Wiegand et al. | Mar 1967 | A |
3309444 | Schueler | Mar 1967 | A |
3493527 | Schueler | Feb 1970 | A |
3516953 | Wood | Jun 1970 | A |
3645939 | Gaylord | Feb 1972 | A |
3671615 | Price | Jun 1972 | A |
3697364 | Boustany | Oct 1972 | A |
3709845 | Boustany | Jan 1973 | A |
3718536 | Downs et al. | Feb 1973 | A |
3836412 | Boustany et al. | Sep 1974 | A |
3878143 | Baumann et al. | Apr 1975 | A |
3888810 | Shinomura | Jun 1975 | A |
3943079 | Hamed | Mar 1976 | A |
3956541 | Pringle | May 1976 | A |
3956555 | McKean | May 1976 | A |
4005162 | Bucking | Jan 1977 | A |
4016232 | Pringle | Apr 1977 | A |
4020212 | Erickson | Apr 1977 | A |
4033913 | Sunden | Jul 1977 | A |
4045603 | Smith | Aug 1977 | A |
4056591 | Goettler et al. | Nov 1977 | A |
4058580 | Flanders | Nov 1977 | A |
4097648 | Pringle | Jun 1978 | A |
4112038 | Garner | Sep 1978 | A |
4113908 | Shinomura | Sep 1978 | A |
4115497 | Halmo et al. | Sep 1978 | A |
4145389 | Smith | Mar 1979 | A |
4168251 | Schinzel et al. | Sep 1979 | A |
4187352 | Klobbie | Feb 1980 | A |
4188259 | Mamers et al. | Feb 1980 | A |
4203876 | Dereppe et al. | May 1980 | A |
4204010 | Kramm et al. | May 1980 | A |
4228116 | Colombo et al. | Oct 1980 | A |
4239679 | Rolls et al. | Dec 1980 | A |
4244847 | Posiviata et al. | Jan 1981 | A |
4244903 | Schnause | Jan 1981 | A |
4248743 | Goettler | Feb 1981 | A |
4248820 | Haataja | Feb 1981 | A |
4250222 | Mavel et al. | Feb 1981 | A |
4263184 | Leo et al. | Apr 1981 | A |
4265846 | Shen et al. | May 1981 | A |
4273688 | Porzel et al. | Jun 1981 | A |
4277428 | Luck et al. | Jul 1981 | A |
4279790 | Nakajima | Jul 1981 | A |
4281039 | Miura et al. | Jul 1981 | A |
4290988 | Nopper et al. | Sep 1981 | A |
4303019 | Haataja et al. | Dec 1981 | A |
4305901 | Prince et al. | Dec 1981 | A |
4311554 | Herr | Jan 1982 | A |
4311621 | Nishizawa et al. | Jan 1982 | A |
4318351 | Munk | Mar 1982 | A |
4323625 | Coran et al. | Apr 1982 | A |
4328136 | Blount | May 1982 | A |
4376144 | Goettler | Mar 1983 | A |
4382108 | Carroll et al. | May 1983 | A |
4393020 | Li et al. | Jul 1983 | A |
4414267 | Coran et al. | Nov 1983 | A |
4420351 | Lussi et al. | Dec 1983 | A |
4426470 | Wessling et al. | Jan 1984 | A |
4440708 | Haataja et al. | Apr 1984 | A |
4454091 | Chion et al. | Jun 1984 | A |
4455709 | Zanini | Jun 1984 | A |
4481701 | Hewitt | Nov 1984 | A |
4491553 | Yamada et al. | Jan 1985 | A |
4503115 | Hemels et al. | Mar 1985 | A |
4505869 | Nishibori | Mar 1985 | A |
4506037 | Suzuki et al. | Mar 1985 | A |
4508595 | Gasland | Apr 1985 | A |
4551294 | Wottka et al. | Nov 1985 | A |
4559376 | Kubat | Dec 1985 | A |
4562218 | Fornadel et al. | Dec 1985 | A |
4594372 | Natov et al. | Jun 1986 | A |
4597928 | Terentiev et al. | Jul 1986 | A |
4608922 | Pohl | Sep 1986 | A |
4610900 | Nishibori | Sep 1986 | A |
4624890 | Lloyd et al. | Nov 1986 | A |
4632170 | Pohl | Dec 1986 | A |
4645631 | Hegenstaller et al. | Feb 1987 | A |
4659754 | Edwards et al. | Apr 1987 | A |
4663225 | Farley et al. | May 1987 | A |
4674414 | Nülle et al. | Jun 1987 | A |
4686251 | Ostermann et al. | Aug 1987 | A |
4687793 | Motegi et al. | Aug 1987 | A |
4716062 | Klein | Dec 1987 | A |
4717742 | Beshay | Jan 1988 | A |
4734236 | Davis | Mar 1988 | A |
4737532 | Fujita et al. | Apr 1988 | A |
4738723 | Frizzell et al. | Apr 1988 | A |
4746688 | Bistak et al. | May 1988 | A |
4769109 | Tellvik et al. | Sep 1988 | A |
4769274 | Tellvik et al. | Sep 1988 | A |
4791020 | Kokta | Dec 1988 | A |
4810445 | Lamb, Sr. et al. | Mar 1989 | A |
4818604 | Tock | Apr 1989 | A |
4833181 | Narukawa et al. | May 1989 | A |
4851458 | Hopperdietzel | Jul 1989 | A |
4865788 | Davis | Sep 1989 | A |
4874095 | Warych | Oct 1989 | A |
4894192 | Warych | Jan 1990 | A |
4911700 | Makoui et al. | Mar 1990 | A |
4915764 | Miani | Apr 1990 | A |
4927579 | Moore | May 1990 | A |
4929498 | Suskind et al. | May 1990 | A |
4935182 | Ehner et al. | Jun 1990 | A |
4960548 | Ikeda et al. | Oct 1990 | A |
4963603 | Felegi, Jr. et al. | Oct 1990 | A |
4968463 | Levasseur | Nov 1990 | A |
4973440 | Tamura et al. | Nov 1990 | A |
4978489 | Radvan et al. | Dec 1990 | A |
4988478 | Held | Jan 1991 | A |
5002713 | Palardy et al. | Mar 1991 | A |
5008310 | Beshay | Apr 1991 | A |
5009586 | Pallmann | Apr 1991 | A |
5028266 | Rettenmaier | Jul 1991 | A |
5057167 | Gersbeck | Oct 1991 | A |
5064692 | Hofmann et al. | Nov 1991 | A |
5075057 | Hoedl | Dec 1991 | A |
5075359 | Castagna et al. | Dec 1991 | A |
5082605 | Brooks et al. | Jan 1992 | A |
5084135 | Brooks et al. | Jan 1992 | A |
5087400 | Theuveny | Feb 1992 | A |
5088910 | Goforth et al. | Feb 1992 | A |
5093058 | Harmon et al. | Mar 1992 | A |
5096046 | Goforth et al. | Mar 1992 | A |
5096406 | Brooks et al. | Mar 1992 | A |
5100545 | Brooks | Mar 1992 | A |
5100603 | Neefe | Mar 1992 | A |
5104411 | Makoui et al. | Apr 1992 | A |
5120776 | Raj et al. | Jun 1992 | A |
5124519 | Roy et al. | Jun 1992 | A |
5134023 | Hsu | Jul 1992 | A |
5137668 | Lamb, Sr. | Aug 1992 | A |
5155147 | Dietz et al. | Oct 1992 | A |
5183837 | Lepori et al. | Feb 1993 | A |
5194461 | Bergquist et al. | Mar 1993 | A |
5213021 | Goforth et al. | May 1993 | A |
5254617 | Inoue et al. | Oct 1993 | A |
5268074 | Brooks et al. | Dec 1993 | A |
5277758 | Brooks et al. | Jan 1994 | A |
5284610 | Tai | Feb 1994 | A |
5285973 | Goforth et al. | Feb 1994 | A |
5298102 | Pohl | Mar 1994 | A |
5331087 | Menges | Jul 1994 | A |
5350370 | Jackson et al. | Sep 1994 | A |
5351895 | Brooks et al. | Oct 1994 | A |
5366790 | Liebel | Nov 1994 | A |
5372878 | Saito | Dec 1994 | A |
5374474 | Pratt et al. | Dec 1994 | A |
5380180 | Lamb, Sr. | Jan 1995 | A |
5406768 | Giuseppe et al. | Apr 1995 | A |
5421205 | Pohl | Jun 1995 | A |
5432000 | Young, Sr. et al. | Jul 1995 | A |
5437766 | Van Phan et al. | Aug 1995 | A |
5439542 | Liebel | Aug 1995 | A |
5439749 | Klasell et al. | Aug 1995 | A |
5441801 | Deaner et al. | Aug 1995 | A |
5480602 | Nagaich | Jan 1996 | A |
5486553 | Deaner et al. | Jan 1996 | A |
5497594 | Giuseppe et al. | Mar 1996 | A |
5498478 | Hansen et al. | Mar 1996 | A |
5516472 | Laver | May 1996 | A |
5516585 | Young, Sr. et al. | May 1996 | A |
5518677 | Deaner et al. | May 1996 | A |
5539027 | Deaner et al. | Jul 1996 | A |
5540244 | Brooks et al. | Jul 1996 | A |
5543205 | Liebel | Aug 1996 | A |
5547745 | Hansen et al. | Aug 1996 | A |
5558933 | Anthony | Sep 1996 | A |
5571618 | Hansen et al. | Nov 1996 | A |
5574094 | Malucelli et al. | Nov 1996 | A |
5582682 | Ferretti | Dec 1996 | A |
5582847 | Peterson et al. | Dec 1996 | A |
5585155 | Heikkila et al. | Dec 1996 | A |
5614570 | Hansen et al. | Mar 1997 | A |
5643359 | Soroushian et al. | Jul 1997 | A |
5643635 | Ahn et al. | Jul 1997 | A |
5663216 | Tomka | Sep 1997 | A |
5695874 | Deaner et al. | Dec 1997 | A |
5746958 | Gustafsson et al. | May 1998 | A |
5759680 | Brooks et al. | Jun 1998 | A |
5767177 | Omente et al. | Jun 1998 | A |
5773138 | Seethamraju et al. | Jun 1998 | A |
5791262 | Knight et al. | Aug 1998 | A |
5819491 | Davis | Oct 1998 | A |
5824246 | Reetz | Oct 1998 | A |
5827607 | Deaner et al. | Oct 1998 | A |
5851469 | Muller et al. | Dec 1998 | A |
5871161 | Nishibori | Feb 1999 | A |
5876641 | LeClair et al. | Mar 1999 | A |
5882564 | Puppin | Mar 1999 | A |
5932334 | Deaner et al. | Aug 1999 | A |
5948505 | Puppin | Sep 1999 | A |
5948524 | Seethamraju et al. | Sep 1999 | A |
5952105 | Medoff et al. | Sep 1999 | A |
5973035 | Medoff et al. | Oct 1999 | A |
5981067 | Seethamraju et al. | Nov 1999 | A |
5985429 | Plummer et al. | Nov 1999 | A |
6004668 | Deaner et al. | Dec 1999 | A |
6007656 | Heikkila et al. | Dec 1999 | A |
6015611 | Deaner et al. | Jan 2000 | A |
6015612 | Deaner et al. | Jan 2000 | A |
6054207 | Finley | Apr 2000 | A |
6106944 | Heikkila et al. | Aug 2000 | A |
6122877 | Hendrickson et al. | Sep 2000 | A |
6207729 | Medoff et al. | Mar 2001 | B1 |
6210792 | Seethamraju et al. | Apr 2001 | B1 |
6258876 | Medoff et al. | Jul 2001 | B1 |
6270883 | Sears et al. | Aug 2001 | B1 |
6270893 | Young, Sr. et al. | Aug 2001 | B1 |
6346160 | Puppin | Feb 2002 | B1 |
6357197 | Serino et al. | Mar 2002 | B1 |
6420626 | Erspamer et al. | Jul 2002 | B1 |
6425979 | Hansen et al. | Jul 2002 | B1 |
6448307 | Medoff et al. | Sep 2002 | B1 |
6521087 | Hansen et al. | Feb 2003 | B1 |
6620503 | Qin et al. | Sep 2003 | B1 |
6670035 | Pittman et al. | Dec 2003 | B1 |
6692825 | Qin et al. | Feb 2004 | B1 |
6730249 | Sears et al. | May 2004 | B1 |
6743507 | Barlow et al. | Jun 2004 | B1 |
6824729 | Oin et al. | Nov 2004 | B1 |
6855182 | Sears | Feb 2005 | B1 |
20020010229 | Medoff et al. | Jan 2002 | A1 |
20020019614 | Woon et al. | Feb 2002 | A1 |
20030032702 | Medoff et al. | Feb 2003 | A1 |
20030121380 | Cowell et al. | Jul 2003 | A1 |
20030125688 | Keane et al. | Jul 2003 | A1 |
20030187102 | Medoff et al. | Oct 2003 | A1 |
Number | Date | Country |
---|---|---|
4781190 | Jan 1989 | AU |
B-4781190 | Jan 1989 | AU |
43 31 747 | Mar 1995 | DE |
43 31 747 | Mar 1995 | DE |
0 161 766 | Nov 1985 | EP |
0 161 766 | Nov 1985 | EP |
0 330 729 | Sep 1988 | EP |
0 409 525 | Jul 1990 | EP |
2104903 | Jan 1983 | GB |
2171953 | Sep 1986 | GB |
60-168611 | Feb 1985 | JP |
61-243805 | Oct 1986 | JP |
61-273805 | Feb 1988 | JP |
63-033441 | Feb 1988 | JP |
63-033442 | Feb 1988 | JP |
63-033448 | Feb 1988 | JP |
63-0334401 | Feb 1988 | JP |
WO 9207022 | Apr 1992 | WO |
WO 9508954 | Mar 1995 | WO |
WO 9613468 | May 1996 | WO |
WO 9613551 | May 1996 | WO |
WO 9706942 | Feb 1997 | WO |
WO 9718173 | May 1997 | WO |
WO 9911453 | Mar 1999 | WO |
WO 9923138 | May 1999 | WO |
WO 0029183 | May 2000 | WO |
WO 0034567 | Jun 2000 | WO |
WO 0214039 | Feb 2002 | WO |
Number | Date | Country | |
---|---|---|---|
20050080168 A1 | Apr 2005 | US |
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---|---|---|---|
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---|---|---|---|
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Parent | 09290031 | Apr 1999 | US |
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Parent | 08961863 | Oct 1997 | US |
Child | 09290031 | US | |
Parent | 08921807 | Sep 1997 | US |
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