The present invention is concerned with conductive composite material for wet electrostatic precipitator (WESP) applications.
Wet electrostatic precipitators have been used for many years to remove dust, acid mist and other particulates from water-saturated air and other gases by electrostatic means. In a WESP, particulates and/or mist laden water-saturated air flows in a region of the precipitator between discharge and collecting electrodes, where the particulates and/or mist are electrically charged by corona emitted from high voltage discharge electrodes. As the water-saturated gas flows further within the WESP, the charged particulate matter and/or mist is electrostatically attracted to grounded collecting plates or electrodes where it is collected. The accumulated materials are continuously washed off by both an irrigating film of water and periodic flushing.
WESPs are used to remove pollutants from gas streams exhausting from various industrial sources, such as incinerators, wood products manufacturing, coke ovens, glass furnaces, non-ferrous metallurgical plants, coal-fired electricity generation plants, forest product facilities, food drying plants and petrochemical plants.
Traditionally, the collecting surfaces and other parts of electrostatic precipitators exposed to the process gas stream have been fabricated from carbon steel, stainless steel, corrosion and temperature resistant alloys and lead. However, such materials tend to corrode and/or degrade over time especially when the precipitators are used in severe environments. Carbon and stainless steel tend to corrode or erode under severe acid conditions. Reinforced thermoplastics tend to erode and/or delaminate due to severe corrosive conditions and localized high temperature in regions of sparking.
Other methods have been used to fabricate collecting surfaces involving the use of plastic materials; however, these materials rely on a continuous water film to ensure electrical grounding of the equipment, which has proved to be a problem. PVC, polypropylene and other similar materials have been used but have suffered from holes and flashover-induced fires and, therefore, are not widely used.
In PCT publications Nos. WO2008/154,735 and WO2010/108,256, assigned to the assignee hereof and incorporated herein by reference, there is described electrically-conductive, corrosion resistant and temperature and spark resistant composite material with good heat dissipation for use in the fabricating components used in WESPs. Such materials generally comprise carbon fiber with a thermosetting resin in a cross-linked structure.
As described therein, the electrically conductive composite material utilized herein is a conductive composite material designed for highly corrosive operating conditions including dry and saturated mist environments with elevated temperatures. The composite material is a blend of carbon fibers and thermosetting resins developed for wet electrostatic precipitation, where such materials are subjected to corona voltage flash over, spark, erosion, corrosion and power arc.
In particular, the composite material comprises carbon fiber within a thermosetting resin where extremely strong molecular building blocks form totally cross-linked structures bonded to each other and at interconnects. The resultant network has proven to withstand high voltage current after the onset of corona in the tubes of the electrostatic precipitator, obtaining voltage flash over without pitting the conductive hybrid composite material. Such spark resistance and arc-over may be generated at a voltage of approximately 60 to 95 KV at up to 500 to 1000 milliamps for a duration of approximately 1 millisecond. The composite material is also resistant to sustained arcing with a duration of up to 4 to 5 seconds. These properties are highly desirable to minimize corrosion and restrict high intensity heat generation and to prevent structural, mechanical or chemical changes to the conductive hybrid composite material.
The carbon fibers woven into a seamless biaxial material sleeve creates a dense network imparting electrical conductivity and thermal dispersion within thermosetting resins.
Strong molecular building blocks form totally cross-linked structures bonded to each other and as interconnects, producing a three-dimensional network, stitched through the thickness of the laminate. The carbon fibers are woven into seamless biaxial and triaxial material. This arrangement imparts excellent electrical conductivity and superior thermal dispersion through the laminate.
In addition to the electro-conductive characteristics and excellent corrosion resistant properties, the conductive hybrid composite material also provides further advantages as a material of construction, reducing the dead load weight by one half or more, due to the lightweight and high strength qualities of carbon fiber which results in economic benefits before installation especially beneficial for tube bundles made from stainless steel and even higher grades of titanium.
The composite may be prepared by weaving, stitching, alignment through vibration using frequency while the material may be formed into shapes that are tubes and sheets by prior art processes known as vacuum infusion, pultrusion, filament winding and autoclaving.
The conductive composite material overcomes the problems of corrosion affecting stainless steel, alloys and titanium within a highly corrosive environment, saturated mists and elevated temperatures, by improving on prior art thermosetting resins and carbon fiberglass compositions that cannot withstand the corona voltage flash over and power arcs at up to 100,000 Volts.
It has now been found that the erosion direction and density on the WESP collecting electrodes prepared from such electrically-conductive, corrosion resistant and temperature and spark resistant material can be controlled by controlling the weave pattern of the carbon fibers and fabric thickness. In this regard, a tighter weave creates a greater density of erosion lines in the collecting electrode while thicker carbon fiber fabrics create erosion lines with fewer turns and branching.
Accordingly, in one aspect of the present invention, there is provided a collecting electrode comprises of an electrically-conductive, corrosion resistant and temperature and spark resistant composite material comprising carbon fiber in a cross-linked thermosetting resin, wherein erosion direction and density on the electrode is controlled.
The control of the erosion density and direction may be effected by controlling the weave pattern and/or fabric thickness of the carbon fibers. The carbon fibers preferably are woven in a 2×2 twill arrangement, but other weave patterns may be used, such as 4×4 twill, plain weave and satin weave, may be used.
Referring to
A capacitor bank was installed in parallel with the hexagonal tube. The capacitance was equivalent to approximately 277 tubes, each 5 m long and 250 mm equivalent diameter. A pointed discharge spike was installed on the mast (emitting) electrode, adjacent to which composite samples were mounted on the test collecting tube. Power arcs generated approximately 67 Joules to be dissipated at the point of arc contact on the sample. The controller on the T/R set was such that arcs could be counted. These power arcs were robust in nature and sufficiently loud that the integrated arc count reading on the controller could be verified using a stopwatch and manual spark count.
This Example describes the test results obtained for 304L stainless steel (SS304L).
A sample constructed of SS304L was tested in the test rig of
This Example shows the effect of fiber weave pattern and fabric thickness on erosion density and direction.
Four samples of composite materials were formed into collecting electrodes and arranged in the power-arc testing rig illustrated in
Overall, the total amount of electrical arc erosion in all of the samples was relatively small compared to the total surface area tested and the thickness of the laminate.
In Sample 1, the cross section of the erosion running in bundle of transverse direction of the fibers was found to be well defined “V” (
With the addition of more arcs (Sample 1 @2120 arcs vs. Sample 2 @10041 arcs), the majority of the traits previously seen were duplicated; however, the length and width of the erosion increased and the maximum observed cross sectional depth of an erosion increased to 364.2 μm. This translates to 11% of the laminate and ⅔ of the surface lamina.
With Samples 1 and 2, the agglomeration of arc erosion formed straight lines running transversely to the targeted surface tow (see
Sample 2, with 10041 arcs, had an additional trend from those seen in Sample 1, with 2120 arcs (see
As for the 1×4 Twill samples, the difference between the arc erosion of Samples B1-A and B1-B (1×4 Twill) and the previously discussed Samples 1 and 2 (2×2 Twill) was the location of the main erosion concentrations. Sample B1-A and B1-B erosion was focused mainly on the tows of the fabric running in the Twill-1 direction and the Twill-4 direction was relatively clear of any major erosion. In contrast to this Sample 1 (2×2 Twill), arc erosion were evenly distributed on both the warp and the weft directions.
The above findings provide the possibility of controlling the erosion density and direction by controlling the fabric weave pattern and the fabric thickness. As seen in Sample 2, each crossover point in the weave contained one erosion line. Hence it can be concluded that a tighter weave creates a greater density of erosion lines. Thicker fabrics will also create erosion lines with fewer turns and branching.
After arc testing of Sample 2 (10041 arcs) the only observation to the naked eye was surface discoloration caused by the sample's loss of luster, or sheen. Since the damage was so small, it was concluded that the new conductive composite has better resistance to arc erosion than SS304L.
This Example shows the arc performance of joints between WESP components.
In the assembly of a WESP from composite carbon fibre materials, components are adhered together using a bonding formulation. The assembly of such WESPs is described in PCT publication No. WO 2011/029186, assigned to the assignee hereof and the disclosure of which is incorporated herein by reference. Formulations for use as the adhesive are described in PCT publication No. WO 2011/147016, assigned to the assignee hereof and the disclosure of which is incorporated herein by reference.
The adhesive bonding of sub components is a major aspect in the assembly of the new WESP design. To evaluate arc performance of the joint, two sample plaques were bonded together using a conductive bonding formulation. One sample had a joint line as thin as possible (<0.25 mm) and another had a thick joint line (approximately 1.25 mm).
Two corrosion resistant conductive bonding formulations were tested, one variant with a blend of conductive carbon fibers and another with a carbon nanotubes/conductive carbon fiber blend, which was formulated to the same material cost point as the first.
Prior to applying the bonding formulation, the substrate plaques were sanded to remove insulative surface resin. The sanding stopped once 80% of the surface showed anisotropic reflection caused by the exposure of the carbon fibers. The conductivity of the surface was tested in multiple locations to confirm that the majority of the insulative resin was removed.
The joints were subjected to 10000 power arcs in the test facility at an electrical condition approximating the full-scale application. Visual observations showed similar arc erosion to the non-bonded laminates, discussed above.
In summary of this disclosure, electrically-conductive, corrosion resistant and temperature and spark resistant composite materials comprising carbon fibre and thermosetting cross-linked resin have improved arc resistance in terms of erosion density and direction by controlling the weave pattern and fabric thickness. Modifications are possible within the scope of this invention.
This application claims the benefit of U.S. Provisional Application No. 61/468,199 to McGrath filed on Mar. 28, 2011, entitled “EROSION-RESISTANT CONDUCTIVE COMPOSITE MATERIAL COLLECTING ELECTRODE FOR WESP”, the entire content of which is incorporated herein by reference.
Filing Document | Filing Date | Country | Kind | 371c Date |
---|---|---|---|---|
PCT/CA2012/000277 | 3/28/2012 | WO | 00 | 2/19/2014 |
Publishing Document | Publishing Date | Country | Kind |
---|---|---|---|
WO2012/129656 | 10/4/2012 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
687109 | Baum | Nov 1901 | A |
710655 | Angell | Oct 1902 | A |
1322163 | Conover | Nov 1919 | A |
1399422 | Chubb | Dec 1921 | A |
1602597 | Staude | Oct 1926 | A |
1773073 | Beach | Aug 1930 | A |
1773973 | Edgar | Aug 1930 | A |
1793664 | Anderson | Feb 1931 | A |
1813637 | Powers | Jul 1931 | A |
2357355 | Penney | Sep 1944 | A |
2567709 | Hedberg | Sep 1951 | A |
2696892 | Campbell | Dec 1954 | A |
2712362 | Winklepleck | Jul 1955 | A |
2720551 | Wastvind et al. | Oct 1955 | A |
2794847 | Streuber et al. | Jun 1957 | A |
2806896 | Streuber et al. | Sep 1957 | A |
2830869 | Limerick | Apr 1958 | A |
2935375 | Boucher | May 1960 | A |
3046716 | Rodger | Jul 1962 | A |
3104963 | Bonnett | Sep 1963 | A |
3297903 | Riek | Jan 1967 | A |
3403497 | Vander Mey | Oct 1968 | A |
3495123 | Raddatz | Feb 1970 | A |
3512340 | Golucke et al. | May 1970 | A |
3584440 | Vigil | Jun 1971 | A |
3595983 | Muller et al. | Jul 1971 | A |
3605386 | Erwin et al. | Sep 1971 | A |
3716966 | De Seversky | Feb 1973 | A |
3721069 | Walker | Mar 1973 | A |
3745751 | Zey et al. | Jul 1973 | A |
3765154 | Hardt et al. | Oct 1973 | A |
3793802 | Hardt | Feb 1974 | A |
3798883 | Heeney | Mar 1974 | A |
3883328 | Spain | May 1975 | A |
3918939 | Hardt | Nov 1975 | A |
4070424 | Olson et al. | Jan 1978 | A |
4117255 | Kawaike et al. | Sep 1978 | A |
4141698 | Kihlstedt et al. | Feb 1979 | A |
4155792 | Gelhaar et al. | May 1979 | A |
4177047 | Goland | Dec 1979 | A |
4247307 | Chang | Jan 1981 | A |
4251682 | Ebert et al. | Feb 1981 | A |
4290738 | Liebert et al. | Sep 1981 | A |
4294591 | Kahl | Oct 1981 | A |
4318719 | Kato et al. | Mar 1982 | A |
4360367 | Prior | Nov 1982 | A |
4375364 | Van Hoesen et al. | Mar 1983 | A |
4431617 | Farin | Feb 1984 | A |
4439216 | Perryman | Mar 1984 | A |
4505776 | Murray | Mar 1985 | A |
4507341 | Heseltine | Mar 1985 | A |
4522634 | Frank | Jun 1985 | A |
4601731 | Michelson | Jul 1986 | A |
4704363 | Ziegler | Nov 1987 | A |
4846857 | Tachibana | Jul 1989 | A |
4885139 | Sparks et al. | Dec 1989 | A |
4893752 | Spink et al. | Jan 1990 | A |
4908047 | Leonard | Mar 1990 | A |
4948399 | Reuffurth et al. | Aug 1990 | A |
4957512 | Denisov et al. | Sep 1990 | A |
5192517 | Spink | Mar 1993 | A |
5248324 | Hara | Sep 1993 | A |
5254155 | Mensi | Oct 1993 | A |
5295310 | Eriksson | Mar 1994 | A |
5308589 | Yung | May 1994 | A |
5344481 | Pettersson | Sep 1994 | A |
5363567 | Best | Nov 1994 | A |
5364457 | Cameron | Nov 1994 | A |
5395430 | Lundgren et al. | Mar 1995 | A |
5401302 | Schulmerich et al. | Mar 1995 | A |
5482540 | Trinward et al. | Jan 1996 | A |
5498462 | Darfler | Mar 1996 | A |
5599508 | Martinelli et al. | Feb 1997 | A |
5603751 | Ackerson | Feb 1997 | A |
5603752 | Hara | Feb 1997 | A |
5714226 | Disselbeck | Feb 1998 | A |
5843210 | Paranjpe et al. | Dec 1998 | A |
5855652 | Talley | Jan 1999 | A |
5917138 | Taylor | Jun 1999 | A |
5922290 | Jenne et al. | Jul 1999 | A |
6004375 | Gutsch et al. | Dec 1999 | A |
6106592 | Paranjpe et al. | Aug 2000 | A |
6156098 | Richards | Dec 2000 | A |
6176902 | Matsubara | Jan 2001 | B1 |
6231643 | Pasic et al. | May 2001 | B1 |
6267802 | Baldrey et al. | Jul 2001 | B1 |
6508861 | Ray | Jan 2003 | B1 |
6579349 | Ting et al. | Jun 2003 | B1 |
6579506 | Spink et al. | Jun 2003 | B2 |
6599349 | Scharkowski | Jul 2003 | B1 |
6620224 | Sato | Sep 2003 | B1 |
6974494 | Zahedi | Dec 2005 | B1 |
7160348 | Allan | Jan 2007 | B2 |
7160358 | Spink et al. | Jan 2007 | B2 |
7938146 | Brooks et al. | May 2011 | B2 |
8597416 | Allan | Dec 2013 | B2 |
20020090873 | Moody | Jul 2002 | A1 |
20030082315 | Mehlman et al. | May 2003 | A1 |
20040139853 | Bologa et al. | Jul 2004 | A1 |
20040169162 | Xiao et al. | Sep 2004 | A1 |
20040221720 | Anderson et al. | Nov 2004 | A1 |
20040226449 | Heckel et al. | Nov 2004 | A1 |
20050028674 | Allan | Feb 2005 | A1 |
20050045038 | Huang | Mar 2005 | A1 |
20050123717 | Shen et al. | Jun 2005 | A1 |
20050229780 | Spink et al. | Oct 2005 | A1 |
20070051237 | Furukawa et al. | Mar 2007 | A1 |
20070201183 | Komatsu et al. | Aug 2007 | A1 |
20070283903 | Bologa et al. | Dec 2007 | A1 |
20090014378 | Hundley et al. | Jan 2009 | A1 |
20090142980 | Chen | Jun 2009 | A1 |
20090241781 | Triscori et al. | Oct 2009 | A1 |
Number | Date | Country |
---|---|---|
643389 | Jun 1962 | CA |
2505248 | May 2004 | CA |
2376335 | May 2000 | CN |
30 27 307 | May 1981 | DE |
102004001463 | Aug 2005 | DE |
553420 | May 1943 | GB |
556 939 | Oct 1943 | GB |
1413127 | Nov 1975 | GB |
5335674 | Nov 1975 | JP |
52-1574 | Jan 1977 | JP |
57194001 | Nov 1982 | JP |
60 149449 | Aug 1985 | JP |
1-258754 | Oct 1989 | JP |
06190300 | Jul 1994 | JP |
10202142 | Apr 1998 | JP |
11151410 | Jun 1999 | JP |
9005027 | May 1990 | WO |
9219380 | Nov 1992 | WO |
9601678 | Jan 1996 | WO |
2005007295 | Jan 2005 | WO |
2005097297 | Oct 2005 | WO |
2006113749 | Oct 2006 | WO |
2008154735 | Dec 2008 | WO |
2010108256 | Sep 2010 | WO |
2011120137 | Oct 2011 | WO |
Entry |
---|
Supplementary European Search Report for European Patent Application No. 12763929.2, dated Nov. 20, 2014. |
Third Chinese Office Action, Jan. 14, 2015, CN Application No. 201080022796.0. |
Written Opinion, Jan. 23, 2006, International Application No. PCT/CA2004/001037. |
International Preliminary Report on Patentability, Jan. 23, 2006, International Application No. PCT/CA2004/001037. |
Written Opinion, Aug. 12, 2005, International Application No. PCT/CA2005/000549. |
International Preliminary Report on Patentability, Aug. 12, 2005, International Application No. PCT/CA2005/000549. |
Communication pursuant to Article 94(3) EPC, Jul. 18, 2012, EP Application No. 04737969.8. |
Communication pursuant to Article 94(3) EPC, Sep. 23, 2009, EP Application No. 04737969.8. |
Written Opinion, May 1, 2006, International Application No. PCT/CA2006/000238. |
International Preliminary Report on Patentability, Oct. 11, 2006, International Application No. PCT/CA2006/000238. |
Written Opinion, Aug. 28, 2006, International Application No. PCT/CA2006/000755. |
International Preliminary Report on Patentability, Nov. 13, 2007, International Application No. PCT/CA2006/000755. |
Communication pursuant to Article 94(3) EPC, Apr. 23, 2014, EP Application No. 05735662.8. |
Communication pursuant to Article 94(3) EPC, Sep. 15, 2011, EP Application No. 05735662.8. |
EPC Examination, Mar. 10, 2009, EP Application No. 05735662.8. |
Supplementary European Search Report, Jul. 12, 2007, EP Application No. 05735662.8. |
Canadian Office Action, Sep. 9, 2010, Canadian Application No. 2562372. |
Canadian Office Action, Jul. 30, 2012, Canadian Application No. 2598187. |
Canadian Office Action, Jun. 14, 2013, Canadian Application No. 2598187. |
Canadian Office Action, Feb. 6, 2014, Canadian Application No. 2598187. |
Response to Communication, Aug. 26, 2014, EP Application No. 06705193.8. |
Communication pursuant to Article 94(3) EPC, Apr. 17, 2014, EP Application No. 06705193.8. |
Canadian Office Action, Feb. 24, 2012, Canadian Application No. 2607978. |
Communication pursuant to Article 94(3) EPC, Dec. 4, 2012, EP Application No. 08741470.6. |
Written Opinion, Jul. 21 2008, International Application No. PCT/CA2008/000752. |
International Preliminary Report on Patentability, Jul. 21 2008, International Application No. PCT/CA2008/000752. |
Written Opinion, Sep. 19, 2008, International Application No. PCT/CA2008/001157. |
International Preliminary Report on Patentability, Sep. 19, 2008, International Application No. PCT/CA2008/001157. |
Canadian Office Action, Mar. 12, 2014, Canadian Application No. 2684781. |
Canadian Office Action, Oct. 2, 2014, Canadian Application No. 2684781. |
EPC Examination, May 14, 2013, EP Application No. 08748166.9. |
Written Opinion, May 31, 2010, International Application No. PCT/CA2010/000377. |
International Preliminary Report on Patentability, May 31, 2010, International Application No. PCT/CA2010/000377. |
Written Opinion, Dec. 22, 2010, International Application No. PCT/CA2010/001404. |
International Preliminary Report on Patentability, Dec. 22, 2010, International Application No. PCT/CA2010/001404. |
Written Opinion, Aug. 17, 2011, International Application No. PCT/CA2011/000599. |
International Preliminary Report on Patentability, Aug. 17, 2011, International Application No. PCT/CA2011/000599. |
Canadian Office Action, Aug. 6, 2012, Canadian Application No. 2750691. |
Canadian Office Action, May 8, 2013, Canadian Application No. 2750691. |
Canadian Office Action, Nov. 20, 2013, Canadian Application No. 2750691. |
Supplementary European Search Report, Sep. 26, 2013, EP Application No. 10755346.3. |
First Chinese Office Action, Aug. 13, 2013, CH Application No. 201080022796.0. |
Second Chinese Office Action, Jul. 30, 2014, CH Application No. 201080022796.0. |
Canadian Office Action, Nov. 4, 2014, Canadian Application No. 2773620. |
Supplementary European Search Report, Dec. 11, 2103, EP Application No. 10 81 4843. |
Written Opinion, Jun. 26, 2012, International Application No. PCT/CA2012/000277. |
International Preliminary Report on Patentability, Jun. 26, 2012, International Application No. PCT/CA2012/000277. |
Supplementary European Search Report, Nov. 3, 2014, International Application No. PCT/CA2012/000277. |
Supplementary European Search Report, Dec. 20, 2103, EP Application No. 10 81 4843.8. |
First Chinese Office Action, Sep. 23, 2013, CH Application No. 201180026189.6. |
Second Chinese Office Action, May 7, 2014, CH Application No. 201180026189.6. |
Response to First Chinese Office Action, CH Application No. 201180026189.6, Jan. 16, 2014. |
Response to Second Chinese Office Action, CH Application No. 201180026189.6, Jul. 30, 2014. |
International Search Report, Jun. 26, 2012 , International Application No. PCT/CA2012/000277. |
Rushton J.D., Sirrine J.E., Collection and Treatment of Odorous Kraft Mill Gases. Paper Trade Journal/ 1972, pp. 36-37. (Dec. 18, 1972). |
Fourth Chinese Office Action, Jul. 30, 2013, CH Application No. 200880013191.8. |
Response to Third Chinese Office Action, CH Application No. 200880013191.8, Apr. 12, 2013. |
Third Chinese Office Action, Apr. 1, 2013, CH Application No. 200880013191.8. |
Response to Second Chinese Office Action, CH Application No. 200880013191.8, May 7, 2014. |
Second Chinese Office Action, Nov. 27, 2013, CH Application No. 200880013191.8. |
Response to First Chinese Office Action, CH Application No. 200880013191.8, Mar. 16, 2010. |
First Chinese Office Action, Apr. 16, 2012, CH Application No. 200880013191.8. |
Perry et al. Chemical Engineers' Handbook (5th Ed.) McGraw-Hill Book Co. USA;15BN 0-67-049478-9; p. 22-4, 1973. |
Notice of Allowance, Dec. 31, 2014, U.S. Appl. No. 13/699,752. |
Notice of Allowance, Jan. 21, 2015, U.S. Appl. No. 13/394,828. |
Canadian Office Action, Mar. 23, 2009, Canadian Patent Application No. 2532640. |
Canadian Office Action, Aug. 5, 2008, Canadian Patent Application No. 2532640. |
Number | Date | Country | |
---|---|---|---|
20140150659 A1 | Jun 2014 | US |
Number | Date | Country | |
---|---|---|---|
61468199 | Mar 2011 | US |