There is a well-recognized need to clean-up contaminants found in ground water, i.e., aquifers and surrounding soil formations. Such aquifers and surrounding soil formations may be contaminated with various constituents including organic compounds such as, volatile hydrocarbons, including chlorinated hydrocarbons such as dichloroethene (DCE), trichloroethene (TCE), and tetrachloroethene (PCE). Other contaminates that can be present include vinyl chloride, 1,1,1 trichloroethane (TCA), and very soluble gasoline additives such as methyl tertiary butyl ether (MTBE). Other contaminants may also be encountered.
According to an aspect of the invention, a method includes delivering a stream of a fluid to a directional microporous diffuser that has a sidewall with microscopic openings and has a partitioned interior region to effect discharge of microbubbles from less than the entire sidewall portion of the directional microporous diffuser.
Other aspects of the invention include the directional microporous diffuser including an elongated member providing the sidewall, the sidewall defining an interior portion of said member and coupled to the first inlet port, a partition member that divides the interior of the elongated member into plural, mutually isolated regions and caps to seal ends of the directional microporous diffuser. The elongated member is a cylinder. The caps support the first inlet port and additional plural inlet ports. The first inlet port and additional plural inlet ports are arranged to be in fluid communication with corresponding ones of the mutually isolated regions of the directional microporous diffuser. A solenoid-controlled distribution valve is coupled to the first inlet ports and additional plural inlet ports. The microporous diffuser can be disposed in a well or injected. The microporous diffuser emits microbubbles having a size in a range of 1 to 200 microns. The partitioning member divides the interior of the elongated member into four quadrants.
According to a further aspect of this invention, an apparatus includes a distribution arrangement to receive a fluid, a directional microporous diffuser, the directional microporous diffuser including an hollow elongated member having a sidewall with a large plurality of microporous openings, a partitioning member disposed in the interior of the hollow elongated member to divide the interior of the hollow elongated member into mutually isolated regions, with the regions being in fluid communication with the distribution arrangement and a control arrangement to control the distribution arrangement to effect discharge of fluid into selected ones of the mutually isolated regions in the elongated member to cause microbubbles to emanate from correspond portions of the sidewall of the directional microporous diffuser.
Other aspects of the invention include an ozone generator coupled to the first port of the directional microporous diffuser to deliver ozone and air as the first and second fluids. The elongated member is a cylinder. Microbubbles emanate from less than the entire sidewall portion of the directional microporous diffuser. The apparatus further includes a first pump to deliver a first stream of first fluid to the distribution arrangement and a second pump to deliver a second stream of a second fluid to the distribution arrangement. The directional microporous diffuser emits microbubbles having a size in a range of 1 to 200 microns.
According to a still further aspect of this invention, apparatus includes an elongated hollow member having a sidewall with a porosity characteristic, a partitioning member disposed within the elongated hollow member to partition the interior of the elongated hollow member into plural, mutually isolated chambers, a first cap with plural inlet ports that are in fluid communication with the plural mutually isolated chambers and an end cap to seal a second end of the directional microporous diffuser.
The sidewalls of the elongated member have a porosity characteristic of less than 200 microns. The sidewalls of the elongated member have a porosity characteristic of less than 100 microns. The directional microporous diffuser emits microbubbles having a size in a range of 0.5 to 80 microns. The sidewall is comprised of a metal or a plastic. The sidewall is of a hydrophobic material. The sidewall is comprised of sintered fused microscopic particles of plastic.
According to a still further aspect of this invention, a directional microporous diffuser includes a first elongated member including at least one sidewall having a plurality of microscopic openings, the sidewall defining an interior hollow portion of said member. The directional microporous diffuser further includes a second elongated member having a second sidewall having a plurality of microscopic openings, the second member being disposed through the hollow region of the first member. The directional microporous diffuser further includes a first partitioning member disposed inside and along a length of the first elongated member to provide a first plurality of isolated chambers and a second partitioning member disposed of the first elongated member and the second elongated member along the length of the first and second elongated members to provide a second plurality of isolated chambers. The directional microporous diffuser further includes an end cap to seal a first end of the directional microporous diffuser and an inlet cap disposed at a second end of directional microporous diffuser for receiving inlet fittings.
Other embodiments include the directional microporous diffuser having a region defined between the first and second elongated members filled with a catalyst suspension material. The directional microporous diffuser of claim has the first and second partitioning members aligned to provide the first plurality of isolated chambers aligned to the second plurality of isolated chambers. The directional microporous diffuser includes the inlet cap includes multiple inlet fittings, a first portion of the multiple inlet fittings in fluid communication with the corresponding chambers in the first member, and a second portion of the multiple inlet fittings in fluid communication with the corresponding chambers in the second member.
One or more advantages can be provided from the above.
While, a non-partitioned microporous diffuser can enlarge its radius of influence (ROI) by placing the non-partitioned microporous diffuser deeper within an aquifer, e.g., a substantial distance below the contaminants, the directional microporous diffuser provides a mechanism that can discharge microbubbles over a broad lateral area while having directional microporous diffuser remain close to contaminated groundwater zones during sparging. The directional microporous diffuser can cover broad lateral areas without diluting its effectiveness, since the oxidant gas emitted from the directional microporous diffuser can be emitted close to the source of contamination. The lateral areas over which the microbubbles are emitted can be larger since all of the microbubbles emitted from the directional microporous diffuser can be directed into one area at a time.
The partitioning member permits microbubbles to emerge from the surface of the directional microporous diffuser over portions of the directional microporous diffuser in accordance with which of the inlet ports of the directional microporous diffuser receives the fluid stream from the outlet ports of the solenoid-controlled valve. The partition member in the directional microporous diffuser together with the solenoid valve permits a gas stream from the central feed to be directed through one, two, three or all four of the quadrants of the directional microporous diffuser. In general, using a single quadrant at a time permits the microbubbles to exit the directional microporous diffuser and provide a generally elliptical shaped zone of influence in the surrounding soil formation. The zone of influence will extend further in a direction perpendicular from the directional microporous diffuser than tangentially from the sidewalls of the directional microporous diffuser
The solenoid-controlled valve can be controlled to rotate the pattern of microbubbles emitted from the directional microporous diffuser. Thus, microbubbles exit from only a first quadrant during a first time period, then only from a second quadrant during a second time period, and so forth. The control can be automated or manual. The directional microporous diffuser allows fewer wells and sparging arrangements to be constructed on a site for a given sparging arrangement capacity, since all of the capacity of the pumps and so forth are directed into a single portion, e.g., quadrant of a microporous diffuser at any one time. The directional microporous diffuser can also be used to direct treatment towards especially high concentrations of contaminants while minimizing treatment materials in areas of lower contaminant concentrations.
The details of one or more embodiments of the invention are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the invention will be apparent from the description and drawings, and from the claims.
Referring now to
The arrangement 10 also includes a mechanism 20 to deliver treatment fluids. The mechanism 20 includes a first compressor 22 and a compressor control mechanism 27. The compressor 22 has a first outlet to feed, via a line 22a, a first fluid, e.g., air into a manifold 23 comprised of three port solenoid controlled mixing valves 25. The compressor 22 includes a second outlet that is coupled, via line 22b to a second source, e.g., an ozone generator 28 to feed ozone (O3) to the solenoid 23.
The three port solenoid controlled mixing valve 25 is coupled to an inlet port of a solenoid-controlled valve 30. The outlets of solenoid-controlled valve 30 are coupled to lines 33 via check valves 32.
The line 22b coupled between the compressor 22 and the ozone generator 28 allows air to enter the ozone generator directly rather than pulling it under siphon.
As shown in
The directional microporous diffuser 50 is fitted tightly inside the casing and in some embodiments the casing itself can be partitioned (not shown). For the embodiments where the casing is partitioned, the directional microporous diffuser 50 is aligned in the casing such that quadrants in the directional microporous diffuser 50 are aligned with quadrants in the casing. In some embodiments, packing material, e.g., sand may be disposed around the directional microporous diffuser 50. In other embodiments, grooves and rails (not shown) can be provided on the casing and directional microporous diffuser respectively, to allow the directional microporous diffuser to slide down the casing in alignment with partitions in the casing. The grooves and rails (not shown) in addition to providing alignment also provide an inherent isolation of the quadrants of the directional microporous diffuser 50 when inserted in the casing 14.
A non-partitioned microporous diffuser can enlarge its radius of influence (ROI) by placing the microporous diffuser deeper within an aquifer, e.g., a substantial distance below the contaminants. However, this approach dilutes the effectiveness of such a microporous diffuser since the oxidant gas emitted from the non-partitioned microporous diffuser travels vertically for some distance in order to reach the contaminants. Along the way some of the oxidant can dissolve or is absorbed or otherwise become ineffective. The directional microporous diffuser 50 provides a mechanism that can cover broad laterally areas while staying close to contaminated groundwater zones.
Referring now to
In either arrangement 10 or 100, the outlet ports of the solenoid-controlled valve 30 are controlled by solenoids that selectively open and close the outlet ports 32a-32d permitting fluid to escape from one or more of the outlet ports 32a-32d. The outlet ports 32a-32d are coupled to feed lines generally 33 that are coupled to inlet fittings on a cap of the directional microporous diffuser 50. The directional microporous diffuser 50 allows microbubbles to be directed in selected directions into a surrounding soil formation 16, as discussed below.
In the embodiment described, a gas stream of ozone and air is delivered to the directional microporous diffuser 50. Other fluid streams could be used including, air, air enhanced with oxygen, a gas and liquid, e.g., hydrogen peroxide, air/ozone enhanced with hydrogen peroxide, or a hydro peroxide and so forth.
In the illustrated embodiments, microbubbles of air and ozone exit from walls of the directional microporous diffuser 50. The microbubbles of air/ozone affect substantial removal of below-mentioned or similar types of contaminants. The arrangement 10 can also include a pump (not shown) that supplies nutrients such as catalyst agents including iron containing compounds such as iron silicates or palladium containing compounds such as palladized carbon. In addition, other materials such as platinum may also be used.
The microbubbles promote rapid gas/gas/water reactions with volatile organic compounds, in which a substrate (catalyst or enhancer) participates in, instead of solely enhancing dissolved (aqueous) disassociation and reactions. The production of microbubbles and selection of appropriate size distribution is provided by using microporous material and a bubble chamber for optimizing gaseous exchange through high surface area to volume ratio and long residence time within the liquid to be treated. The equipment promotes the continuous production of microbubbles while minimizing coalescing or adhesion.
The injected air/ozone combination moves as a fluid into the material to be treated. The use of microencapsulated ozone enhances and promotes in-situ stripping of volatile organics and simultaneously terminates the normal reversible Henry s reaction. The process involves promoting simultaneous volatile organic compounds (VOC) in-situ stripping and gaseous decomposition, with moisture (water) and substrate (catalyst or enhancer). The basic chemical reaction mechanism of air/ozone encapsulated in micron-sized bubbles is further described in several of my issued patents such as U.S. Pat. No. 6,596,161 “Laminated microporous diffuser”; U.S. Pat. No. 6,582,611 “Groundwater and subsurface remediation”; U.S. Pat. No. 6,436,285 “Laminated microporous diffuser”; U.S. Pat. No. 6,312,605 “Gas-gas-water treatment for groundwater and soil remediation”; and U.S. Pat. No. 5,855,775, “Microporous diffusion apparatus” all of which are incorporated herein by reference.
The compounds commonly treated are HVOCs (halogenated volatile organic compounds), PCE, TCE, DCE, vinyl chloride (VC), EDB, petroleum compounds, aromatic ring compounds like benzene derivatives (benzene, toluene, ethylbenzene, xylenes). In the case of a halogenated volatile organic carbon compound (HVOC), PCE, gas/gas reaction of PCE to by-products of HCl, CO2 and H2O accomplishes this. In the case of petroleum products like BTEX (benzene, toluene, ethylbenzene, and xylenes), the benzene entering the bubbles reacts to decompose to CO2 and H2O.
Also, pseudo Criegee reactions with the substrate and ozone appear effective in reducing saturated olefins like trichloro alkanes (1,1,1-TCA), carbon tetrachloride (CCl4), chloroform methyl chloride, and chlorobenzene, for instance.
Other contaminants that can be treated or removed include hydrocarbons and, in particular, volatile chlorinated hydrocarbons such as tetrachloroethene, trichloroethene, cisdichloroethene, transdichloroethene, 1-1-dichloroethene and vinyl chloride. In particular, other materials can also be removed including chloroalkanes, including 1,1,1 trichloroethane, 1,1, dichloroethane, methylene chloride, and chloroform. Also, aromatic ring compounds such as oxygenates such as O-xylene, P-xylene, naphthalene and methyltetrabutylether (MTBE), ethyltetrabutylether (ETBE), and tertiaryamyltylether (TAME) can be treated.
Ozone is an effective oxidant used for the breakdown of organic compounds in water treatment. The major problem in effectiveness is that ozone as a dissolved species has a short lifetime. If ozone is mixed with sewage containing water above ground, the half-life is normally minutes. Ozone reacts quantitatively with PCE to yield breakdown products of hydrochloric acid, carbon dioxide, and water.
To offset the short life span, the ozone is injected with directional microporous diffusers, enhancing the selectiveness of action of the ozone. By encapsulating the gaseous ozone in fine bubbles, the ozone may have a 2-day half-life at normal (20°) temperatures. The bubbles preferentially extract a vapor phase fraction of the volatile compounds organic compounds they encountered. With this process, a vapor phase according to a partition governed by Henry's Law, of the volatile organics are selectively pulled into the fine air-ozone bubbles. The gas that enters a small bubble of volume (4πr3) increases until reaching an asymptotic value of saturation. The ozone in the bubbles attacks the volatile organics, generally by a Criegee or Criegee-like reaction.
The following characteristics of the contaminants appear desirable for reaction:
Henry's Constant: 10−2 to 10−5 m3 atm−m3/mol
Solubility: 10 to 20,000 mg/l
Vapor pressure: 1 to 3000 mmHg
Saturation concentration: 5 to 9000 g/m3
The production of microbubbles and selection of appropriate size distribution are selected for optimized gas exchange through high surface area to volume ratio and long residence time within the area to be treated.
Referring now to
The partitioning member 60 permits microbubbles to emerge from the surface of the directional microporous diffuser 50 over four, here equally sized quadrants. The microbubbles emerge from the quadrants in accordance with which on the inlet ports 52a-52d of the directional microporous diffuser 50 receives the fluid stream from the outlet ports 32a-32d of the solenoid-controlled valve 30.
Proximate ends of the cylindrical members 56 are coupled to inlet ports generally denoted as 52a. The inlet ports 52a are supported on an inlet cap 52 that seals one end of the cylindrical member 56. The inlet ports 52a are arranged in relation to the four mutually isolated chambers 60a-60d provided within the directional microporous diffuser 50 such that the inlet ports 52a allow a fluid delivered to the inlet ports 52a to enter the respective chamber in the interior of the directional microporous diffuser. In one embodiment, the fluid delivered to the inlet ports 52a is a mixture of air and ozone, as described above. At the opposite end of the directional microporous diffuser 50 an end cap 54 covers the second, distal end of cylindrical member 56. Together end cap 54 and cap 52 seal the ends of the directional microporous diffuser 50. While, the cylindrical member 56 is disclosed as being cylindrical in shape, in general the configuration could have other shapes. The partitioning member 60 can extend beyond the length of the cylindrical member such that ends of the partitioning member 60 sit in grooves provided in caps 52 and 54.
The cylindrical member 56 has a plurality of microscopic openings constructed through sidewalls 56a. The openings generally have a pore sizes matched to a surrounding ground formation so as to be effective for inducing gas/gas reactions with introduction of the microbubbles. Sidewalls of each of the cylindrical members can have a pore diameter in a range of 1-200 microns, preferably 1-80 microns and more preferably 1-20 microns. The combination of the inlet cap 52 and end cap 54 seals the directional microporous diffuser 50 permitting the microbubbles to escape only via the porous construction of the sidewalls of the directional microporous diffusers.
The partition member 60 in the directional microporous diffuser 50 together with the solenoid valve 30 permits a gas stream from the central feed to be directed through one, two, three or all four of the quadrants of the directional microporous diffuser 50. Thus, the pattern of the gas stream that exits from the directional microporous diffuser can be adjusted. In general, using a single quadrant at a time permits the bubbles to exit the directional microporous diffuser and have a generally elliptical shaped zone of influence in the surrounding soil formation, that is the zone of influence will extend further in a direction perpendicular from the directional microporous diffuser 50 that tangentially from the sidewalls of the directional microporous diffuser 50. The treatment zone has a longer radius perpendicular to the surface of the directional microporous diffuser than the treatment zone that could be provided were the arrangement used with a non partitioned, non directional microporous diffuser.
The solenoid-controlled valve 30 can be controlled to rotate the pattern of microbubbles emitted from the directional microporous diffuser 50 by permitting microbubbles to exit from only a first quadrant, then only a second quadrant, and so forth. The control can be automated or manual. The directional microporous diffuser 50 allows fewer wells and sparging arrangements 10 to be constructed on a site for a given sparging arrangement capacity by directing all of the capacity of the pumps and so forth into a single quadrant of a directional microporous diffuser at any one time. The directional microporous diffuser 50 can also be used to direct treatment towards especially high concentrations of contaminants while minimizing treatment materials in areas of lower contaminant concentrations. Once a first region is treated, the solenoid can be activated to close the outlet that feeds the first quadrant that treated the first region and open a second outlet of the solenoid to feed a second, different quadrant and treat a second different region.
Referring now to
The fittings (e.g., the inlets in
Referring now to
The directional microporous diffuser 70 has the inner cylindrical member 76 disposed coaxial or concentric to cylindrical member 78. Sidewalls of each of the cylindrical members 76, 78 can have a pore diameter in a range of 1-200 microns, preferably 1-50 microns and more preferably 5-20 microns. A proximate end of the inner cylindrical member is coupled to inlet ports 72a, which are fed an air ozone mixture from the first solenoid valve 30. The directional microporous diffuser also includes an end cap 74, which secures distal ends of the cylinders 76 and 78. The combination of the inlet cap 72 and end cap 74 seals the directional microporous diffuser permitting liquid and gas to escape by the porous construction of sidewalls of the directional microporous diffusers.
The partition members 71 and 73 in the directional microporous diffuser 70 together with the solenoid valve 30 permit a gas stream to be directed through one, two, three or all four of the quadrants of inner member 78. The gas stream that exits from inner member 78 enters outer quadrants between the inner and outer members where it mixes with, e.g., liquid to coat the microbubbles with a liquid coating of, e.g., water or hydrogen peroxide or a hydro peroxide. In general, using a single quadrant at a time permits the coated microbubbles to exit the directional microporous diffuser 70 over the sidewall surface of a single quadrant. The coated microbubbles cover a generally elliptical shaped zone of influence in the surrounding soil formation, as discussed above for directional microporous diffuser 50.
In some embodiments of the microporous diffuser 70, one of the partitioning members can be eliminated to simplify construction of the microporous diffuser 70.
Referring to
Otherwise, the arrangement 120, as shown in
A number of embodiments of the invention have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of the invention.
Number | Name | Date | Kind |
---|---|---|---|
1920719 | Stich | Aug 1933 | A |
2517525 | Cummings | Aug 1950 | A |
2845185 | Winderweedle, Jr. | Jul 1958 | A |
2946446 | Herbert | Jul 1960 | A |
3027009 | Price | Mar 1962 | A |
3206178 | Lamb | Sep 1965 | A |
3219520 | Box | Nov 1965 | A |
3276994 | Andrews | Oct 1966 | A |
3441216 | Good | Apr 1969 | A |
3570218 | Finney | Mar 1971 | A |
3669276 | Woods | Jun 1972 | A |
3708206 | Hard et al. | Jan 1973 | A |
3814394 | Murray | Jun 1974 | A |
3823776 | Holmes | Jul 1974 | A |
3997447 | Breton et al. | Dec 1976 | A |
4007118 | Ciambrone | Feb 1977 | A |
4021347 | Teller et al. | May 1977 | A |
4048072 | McCullough | Sep 1977 | A |
4049552 | Arff | Sep 1977 | A |
4064163 | Drach et al. | Dec 1977 | A |
4178239 | Lowther | Dec 1979 | A |
4203837 | Hoge et al. | May 1980 | A |
4268283 | Roberts | May 1981 | A |
4298467 | Gartner et al. | Nov 1981 | A |
4310057 | Brame | Jan 1982 | A |
4351810 | Martinez et al. | Sep 1982 | A |
4360234 | Hsueh et al. | Nov 1982 | A |
4614596 | Wyness | Sep 1986 | A |
4622139 | Brown | Nov 1986 | A |
4639314 | Tyer | Jan 1987 | A |
4684479 | D'Arrigo | Aug 1987 | A |
4695447 | Shultz | Sep 1987 | A |
4696739 | Pedneault | Sep 1987 | A |
4730672 | Payne | Mar 1988 | A |
4804050 | Kerfoot | Feb 1989 | A |
4832122 | Corey et al. | May 1989 | A |
4837153 | Laurenson, Jr. | Jun 1989 | A |
4838434 | Miller et al. | Jun 1989 | A |
4844795 | Halwani | Jul 1989 | A |
4851163 | Stanton et al. | Jul 1989 | A |
4883589 | Konon | Nov 1989 | A |
4941957 | Zeff et al. | Jul 1990 | A |
4943305 | Bernhardt | Jul 1990 | A |
4960706 | Bliem et al. | Oct 1990 | A |
4966717 | Kern | Oct 1990 | A |
4971731 | Zipperian | Nov 1990 | A |
5078921 | Zipperian | Jan 1992 | A |
5080805 | Houser | Jan 1992 | A |
5116163 | Bernhardt | May 1992 | A |
5120442 | Kull et al. | Jun 1992 | A |
5122165 | Wang | Jun 1992 | A |
5126111 | Al-Ekabi et al. | Jun 1992 | A |
5133906 | Louis | Jul 1992 | A |
5160655 | Donker et al. | Nov 1992 | A |
5167806 | Wang et al. | Dec 1992 | A |
5178755 | Lacrosse | Jan 1993 | A |
5180503 | Gorelick et al. | Jan 1993 | A |
5205927 | Wickramanayake | Apr 1993 | A |
5215680 | D'Arrigo | Jun 1993 | A |
5221159 | Billings et al. | Jun 1993 | A |
5227184 | Hurst | Jul 1993 | A |
5238437 | Vowles et al. | Aug 1993 | A |
5246309 | Hobby | Sep 1993 | A |
5248395 | Rastelli et al. | Sep 1993 | A |
5254253 | Behmann | Oct 1993 | A |
5269943 | Wickramanayake | Dec 1993 | A |
5277518 | Billings et al. | Jan 1994 | A |
5302286 | Semprini et al. | Apr 1994 | A |
5332333 | Bentley | Jul 1994 | A |
5362400 | Martinell | Nov 1994 | A |
5364537 | Paillard | Nov 1994 | A |
5375539 | Rippberger | Dec 1994 | A |
5389267 | Gorelick et al. | Feb 1995 | A |
5398757 | Corte et al. | Mar 1995 | A |
RE34890 | Sacre | Apr 1995 | E |
5402848 | Kelly | Apr 1995 | A |
5403476 | Bernhardt | Apr 1995 | A |
5406950 | Brandenburger et al. | Apr 1995 | A |
5425598 | Pennington | Jun 1995 | A |
5427693 | Mausgrover et al. | Jun 1995 | A |
5430228 | Ciambrone et al. | Jul 1995 | A |
5431286 | Xu et al. | Jul 1995 | A |
5451320 | Wang et al. | Sep 1995 | A |
5464309 | Mancini et al. | Nov 1995 | A |
5472294 | Billings et al. | Dec 1995 | A |
5480549 | Looney et al. | Jan 1996 | A |
5520483 | Vigneri | May 1996 | A |
5525008 | Wilson | Jun 1996 | A |
5545530 | Satomura et al. | Aug 1996 | A |
5560737 | Schuring et al. | Oct 1996 | A |
5588490 | Suthersan et al. | Dec 1996 | A |
5609798 | Liu et al. | Mar 1997 | A |
5615974 | Land et al. | Apr 1997 | A |
5620593 | Stagner | Apr 1997 | A |
5622450 | Grant et al. | Apr 1997 | A |
5624635 | Pryor | Apr 1997 | A |
5663475 | Elgal | Sep 1997 | A |
5664628 | Koehler et al. | Sep 1997 | A |
5667733 | Waldron, Sr. | Sep 1997 | A |
5676823 | McKay et al. | Oct 1997 | A |
5698092 | Chen | Dec 1997 | A |
5827485 | Libal et al. | Oct 1998 | A |
5833388 | Edwards et al. | Nov 1998 | A |
5851407 | Bowman et al. | Dec 1998 | A |
5855775 | Kerfoot | Jan 1999 | A |
5860598 | Cruz | Jan 1999 | A |
5879108 | Haddad | Mar 1999 | A |
5925257 | Albelda et al. | Jul 1999 | A |
5954452 | Goldstein | Sep 1999 | A |
5967230 | Cooper et al. | Oct 1999 | A |
6007274 | Suthersan | Dec 1999 | A |
6017449 | Eriksson et al. | Jan 2000 | A |
6083403 | Tang et al. | Jul 2000 | A |
6083407 | Kerfoot | Jul 2000 | A |
6086769 | Kilambi et al. | Jul 2000 | A |
6136186 | Gonzalez-Martin et al. | Oct 2000 | A |
6139755 | Marte et al. | Oct 2000 | A |
6210955 | Hayes | Apr 2001 | B1 |
6214240 | Yasunaga et al. | Apr 2001 | B1 |
6217767 | Clark | Apr 2001 | B1 |
6254310 | Suthersan | Jul 2001 | B1 |
6283674 | Suthersan | Sep 2001 | B1 |
6284143 | Kerfoot | Sep 2001 | B1 |
6306296 | Kerfoot | Oct 2001 | B1 |
6312605 | Kerfoot | Nov 2001 | B1 |
6352387 | Briggs et al. | Mar 2002 | B1 |
6357670 | Ganan-Calvo | Mar 2002 | B2 |
6364162 | Johnson | Apr 2002 | B1 |
6391259 | Malkin et al. | May 2002 | B1 |
6403034 | Nelson et al. | Jun 2002 | B1 |
6428694 | Brown | Aug 2002 | B1 |
6436285 | Kerfoot | Aug 2002 | B1 |
6447676 | Kerfoot | Sep 2002 | B1 |
6488850 | Perriello | Dec 2002 | B2 |
6582611 | Kerfoot | Jun 2003 | B1 |
6596161 | Kerfoot | Jul 2003 | B2 |
6623211 | Kukor et al. | Sep 2003 | B2 |
6645450 | Stoltz et al. | Nov 2003 | B2 |
6733207 | Liebert, Jr. et al. | May 2004 | B2 |
6736379 | Wegner et al. | May 2004 | B1 |
6773609 | Hashizume | Aug 2004 | B1 |
6780329 | Kerfoot | Aug 2004 | B2 |
6787038 | Brusseau et al. | Sep 2004 | B2 |
6805798 | Kerfoot | Oct 2004 | B2 |
6818136 | Marek | Nov 2004 | B1 |
6827861 | Kerfoot | Dec 2004 | B2 |
6866781 | Schindler | Mar 2005 | B2 |
6872318 | Kerfoot | Mar 2005 | B2 |
6913251 | Kerfoot | Jul 2005 | B2 |
6984329 | Kerfoot | Jan 2006 | B2 |
7022241 | Kerfoot | Apr 2006 | B2 |
7033492 | Kerfoot | Apr 2006 | B2 |
7131638 | Kerfoot | Nov 2006 | B2 |
7156984 | Kerfoot | Jan 2007 | B2 |
7208090 | Applegate et al. | Apr 2007 | B2 |
7264747 | Kerfoot | Sep 2007 | B2 |
7300039 | Kerfoot | Nov 2007 | B2 |
7401767 | Kerfoot | Jul 2008 | B2 |
20020029493 | Baek | Mar 2002 | A1 |
20020109247 | Jager et al. | Aug 2002 | A1 |
20030029792 | Kerfoot | Feb 2003 | A1 |
20030222359 | Jager | Dec 2003 | A1 |
20040045911 | Kerfoot | Mar 2004 | A1 |
20050067356 | Bowman et al. | Mar 2005 | A1 |
20060243668 | Miller et al. | Nov 2006 | A1 |
Number | Date | Country |
---|---|---|
0402158 | Dec 1990 | EP |
0546335 | Jun 1993 | EP |
2005655 | Apr 1979 | GB |
2185901 | Aug 1987 | GB |
4-171036 | Jun 1992 | JP |
6-023378 | Jan 1994 | JP |
409313814 | Dec 1997 | JP |
WO 9821152 | May 1998 | WO |
WO 9954258 | Oct 1999 | WO |
WO2005063367 | Jul 2005 | WO |
Number | Date | Country | |
---|---|---|---|
20070105492 A1 | May 2007 | US |