US2777761A - Composition for eliminating slag, soot, and fly ash - Google Patents
Composition for eliminating slag, soot, and fly ash Download PDFInfo
- Publication number
- US2777761A US2777761A US434349A US43434954A US2777761A US 2777761 A US2777761 A US 2777761A US 434349 A US434349 A US 434349A US 43434954 A US43434954 A US 43434954A US 2777761 A US2777761 A US 2777761A
- Authority
- US
- United States
- Prior art keywords
- boiler
- soot
- slag
- composition
- deposits
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title description 28
- 239000002893 slag Substances 0.000 title description 27
- 239000004071 soot Substances 0.000 title description 25
- 239000010881 fly ash Substances 0.000 title description 13
- 150000001875 compounds Chemical class 0.000 description 23
- 238000002485 combustion reaction Methods 0.000 description 19
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 14
- 229910052799 carbon Inorganic materials 0.000 description 13
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 12
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- 239000002956 ash Substances 0.000 description 7
- 239000003245 coal Substances 0.000 description 6
- 239000000470 constituent Substances 0.000 description 6
- 239000011780 sodium chloride Substances 0.000 description 6
- 235000019270 ammonium chloride Nutrition 0.000 description 5
- 239000011449 brick Substances 0.000 description 5
- 239000002023 wood Substances 0.000 description 5
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 239000000567 combustion gas Substances 0.000 description 4
- 229960000355 copper sulfate Drugs 0.000 description 4
- 229910000365 copper sulfate Inorganic materials 0.000 description 4
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 4
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 4
- 235000013312 flour Nutrition 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 239000011707 mineral Substances 0.000 description 4
- 235000010755 mineral Nutrition 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000005749 Copper compound Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 150000001880 copper compounds Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 238000009434 installation Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000003575 carbonaceous material Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 239000000571 coke Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 229960003280 cupric chloride Drugs 0.000 description 2
- 239000003517 fume Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000004901 spalling Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 235000002918 Fraxinus excelsior Nutrition 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 235000010210 aluminium Nutrition 0.000 description 1
- 150000003868 ammonium compounds Chemical class 0.000 description 1
- -1 ammonium halide Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000001055 blue pigment Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 235000012255 calcium oxide Nutrition 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 239000010883 coal ash Substances 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 229940108928 copper Drugs 0.000 description 1
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 1
- CYKLGTUKGYURDP-UHFFFAOYSA-L copper;hydrogen sulfate;hydroxide Chemical compound O.[Cu+2].[O-]S([O-])(=O)=O CYKLGTUKGYURDP-UHFFFAOYSA-L 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 229940045803 cuprous chloride Drugs 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 206010022000 influenza Diseases 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-UHFFFAOYSA-N 0.000 description 1
- 235000012245 magnesium oxide Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical class [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/06—Use of additives to fuels or fires for particular purposes for facilitating soot removal
Definitions
- the present invention relates to compositions for the removal of carbon (soot) deposits, slag, and fly ash from boiler-tubes, fines, chimneys, walls, superheater banks, etc. of boiler and furnace installations.
- the scale usually consists of mineral deposits, such as ashes of the coal or coke, while the soot is primarily a mixture of large amounts of carbon and smaller amounts of heavy hydrocarbons.
- the soot is usually quite combustible, and, particularly in chimneys, presents a definite fire hazard, for, when once ignited, it burns with great intensity,.and such a fire, particularly in case of a defective chimney or line, may lead to ignition of the building.
- the scale or slag is mainly composed of silica in combination with iron, aluminum, calcium and magnesium oxides.
- It preferably should have a bulk density of less than 4. It should be composed of a material which, when subjected to heat, will produce a chemical reaction which will render all of the constituents of the mixture volatile so that the resultant gas or vapor will be capable of passacting upon slag, carbon, soot, fly ash, and other lay-products of the combustion of coal and fuel back passes of the boiler as well.
- the composition In addition to the mixtureof chemicals containedin the composition it will also act in the combustion chamber as a catalyst serving to assist in the burning'of soot and carbon deposits, primarily by reason of the lowering of the temperatureof ignition of carbon by severalhundred degrees Fahrenheit.
- compositions of the present invention comprise mixtures of a volatile ammonium salt, a copper salt, and a combustible carrier material, with or without an inert coloring material.
- Cupric-chloride maybe substituted for the coppersulfate.
- the wood flour is preferably about mesh in size, as is the copper sulfate, while the ammonium may be about 20 mesh.
- cupric chloride cuprous chloride, copper of finely ground as spacing agents to avoid too intimate contact between the ammonium halide and the copper compound, for if this were permitted to take place, the mixture might cake and harden up. If the reddish color of the iron oxide should not be deemed desirable, other minerals such as chromium oxide (green), chromates (yellow), ochre (brown), or a blue pigment, or any suitable color lake may be used.
- compositions of the present invention may be employed in a number of different ways. They may be sprinkled on top of the fire in a coal-fired furnace or boiler. They may be blown into the space above or behind the fire, such as into the firebox, lines or passages which the combustion gases traverse on their way to the chimney. They may be introduced at definite intervals, say every four, six, eight, twelve, or twenty-four hours, or sma quantities may be introduced at shorter intervals. The introduction may be at several points in the boiler setting at the same time. The amount used depends entirely upon the size of the installation which is to be treated.
- the draft should be increased so that sufficient oxygen may be available to burn up the carbon (soot) deposits which have accumulated'on the lines, walls, on the water-tubes of a boiler, or in the fire tubes thereof. It required some of the composition can be introduced into the back reaches of a boiler setting, so as to treat that portion and perhaps also some of the chimney surfaces themselves.
- composition comprises a volatile and easily dissociated material in the form of ammonium chloride,
- the mixture When used in furnace or boiler installations fired by means of oil or gas, the mixture may advantageously be injected at or close to the point of combustion.
- the combustible ingredient of the composition such as the wood flour, will'furnish additional heat as the result of its own combustion; also acting as a physical carrier for the inorganic constituents until they attain a temperature sufficiently high to cause them to react and/or volatilize.
- the vapors liberated from the composition reach the cooler portions of the boiler, fines, etc., they tend to disintegrate the slag and eliminate the fly ash.
- the slag becomes disintegrated while the ignition temperature of the carbonaceous material'in the soot is-lowered so that it will ignite and burn up. The local areas of heat thus produced will further aid in the loosening and breaking up of the slag.
- the material when applied to or at any designated area the material will instantly volatilize and commence its action upon the surface of which it is applied almost immediately.
- compounds containing sodium chloride such as have been used in the prior art, cannot be applied in this manner. In the first place they have a density of over 1 so that when injected into the furnace or combustion chamber they immediately fall onto the floor or upon the grate.
- volatility as they do possess is a rather slow process making their application at specific areas substantially impossible;
- composition which is of such a physical structure that the treatment of any specific spots or areas in a boiler will be under the absolute control of the operator.
- Fly ash is a fine powdered ash which is carried through the different passes of a boiler, becoming deposited in all of the passages as a result of the decrease in the velocity of the air and combustion gases in their passage through the combustion zone and the back passes of the boiler. It is particularly liable to deposit in the breech of the stack and also on the economizer; in fact it often deposits so heavily upon the latter as to make it temporarily useless.
- the fly ash will be broken up into such a fine dust that it will remain suspended and thus pass through all the passes of the boiler to be eliminated out of the top of the stack. As a result of this, both the breeching and economizer remain free of fly ash so that the passage of the air and combustion gases will be unimpeded.
- Slag dep0sits.,D'epending upon thetype of coal burned more or less slag becomes deposited on the tubes, walls, super-heater banks and other parts of the combustion chamber. This is common in all types of boilers, the quality of the coal being a primary factor.
- the slag or fusion point of the coal ash is variable; some coals have an ash which is readily fusible while other coals have an ash which fuses at a comparatively high temperature. However, no furnace or combustion chamber will long remain free of slag, as slagging will take place to a greater or less degree.
- the superheater banks and the economizer also have to be cleaned, and the fly ash deposits removed. All of be desired, and several thousands of dollars a-zyear can be saved in'operatm'gexpenses if. th'e boiler canbeial ash, soot and other deposits. Dependingnpon the amount of water evaporated 'per day, asmuch as $20.00 peizday can be saved when the' superheater temperatures are .kept at their predetermined .point. All these'desirable effects can be attained by the use of the compound ofthewpresent invention. Moreover, the amount of compound used is also important. It has been found that under average operating conditions the use of as little as 1 pound of the compound per H. P. per day will keep the boiler clean and the operation eflicient.
- the application of the compound is not limited to just the areas close to the tire box or grate for it may be used in any part of the boiler where conditions indicate that a deposit exists or is forming and operator.
- Soot and carbomAoot and carbon deposits are formed on certain areas in all boilers, even those operating on oil. Ordinarily this is eliminated by the use of so-called soot blowers. Tthis procedure is usually done at night because of the fact that the clouds of black sooty carbonaceous material blown out of the boiler cannot be seen, but it nevertheless escapes from the boiler and settles upon the adjacent area.
- the use of the compound of the present invention will get rid of all soot and carbon deposits by reason of the catalytic action of the vapors produced by the volatilization of the material in the present compound which cause the carbon and soot to ignite at a fairly low temperature and thus to burn away to form carbon dioxide which freely escapes in the form of a gas.
- suflicient draft should be available to supply the oxygen required for the elfective combustion of the soot.
- the combustible carrier by being very finely divided, will of course also be air borne and by its own combustion will generate heat which serves further to increase the volatilization of the volatile constituents of the mixture.
- the carrier has little ash of its own, such as in the case of wood flour, or ground corn cobs, or starches, it will of course in no way cause any deposits of its own.
- the entire mixture introduced into the furnace eventually passes out through the stack, together with the material which it is desired to eliminate, thus leaving the furnace walls, tubes, superheater and the various reaches of the boiler in clean and serviceable condition, so as to obtain the best possible heat transfer between the heat of the combustion gases and the heat absorbing metal parts of the boiler.
- a fly ash, slag, soot and carbon eliminator which is extremely light, has a density of not over 0.40, is capable of being air borne and which is extremely volatile in the combustion chamber and back passes of a boiler, comprising from about 40% to 50% by weight of ammonium chloride, about %'to of copper sulfate, about to of wood flour, and enough mineral coloring matter to make References Cited in the file of this patent UNITED STATES PATENTS OTHER REFERENCES Removal of Soot from Furnaces and'Flues by the Use of Salts or Compounds, U.'S. Dept of Commerce, Bureau of Mines, Bulletin 360, pages 3, 8-10, 23-25, 29.
Description
.which not only .ing through and United States Patent O COMPOSITION FOR ELEMlNATING SLAG, SOOT, AND FLY ASH 1 Claim. (Cl. 44-5) The present invention relates to compositions for the removal of carbon (soot) deposits, slag, and fly ash from boiler-tubes, fines, chimneys, walls, superheater banks, etc. of boiler and furnace installations.
It is well known that in the operation of heating systems, the boilers, furnaces and the like, in which fuel, such as coal, coke, oil or gas is burned, gradually become fouled with deposits of soot and scale. The scale usually consists of mineral deposits, such as ashes of the coal or coke, while the soot is primarily a mixture of large amounts of carbon and smaller amounts of heavy hydrocarbons. The soot is usually quite combustible, and, particularly in chimneys, presents a definite fire hazard, for, when once ignited, it burns with great intensity,.and such a fire, particularly in case of a defective chimney or line, may lead to ignition of the building. The scale or slag is mainly composed of silica in combination with iron, aluminum, calcium and magnesium oxides.
Many preparations have been described in the past, which were intended for the removal of these deposits of soot and slag. Most of these were predicated upon the form fumes or" sodium chloride.
It is one of the objects of the present invention to prepare a combustion chamber, a-flue and chimney cleaning composition of greatly improved characteristics, andtone tends to loosen and disintegrate adherent slag and soot but which will also lower the ignition point of carbon.
It is a further objectto provide a method for the cleanmg 0 In order to provide the proper characteristics ina coming characteristics:
1. Extremely high volatility in the combustion chamber of a boiler.
2. It must be a very light fiufiy powder which is easily air borne.
3. It preferably should have a bulk density of less than 4. It should be composed of a material which, when subjected to heat, will produce a chemical reaction which will render all of the constituents of the mixture volatile so that the resultant gas or vapor will be capable of passacting upon slag, carbon, soot, fly ash, and other lay-products of the combustion of coal and fuel back passes of the boiler as well.
5. By reason of its light and fiufiy property it must be capable of application to any desired spot or areain the combustion chamber or back asses of a boiler, primarily by reason of the fact that it is air borne. draft existing in the boiler should besuflicient'to carry The natural 7 2,777,761 Patented Jan. 15, 1 957 the composition along with it so that none of it will-be wasted by falhngto the grate or lower areas-of the cornto have not been attained in a mixture such as that forming the'subject matter or" the present invention.
'8. In addition to the mixtureof chemicals containedin the composition it will also act in the combustion chamber as a catalyst serving to assist in the burning'of soot and carbon deposits, primarily by reason of the lowering of the temperatureof ignition of carbon by severalhundred degrees Fahrenheit.
The compositions of the present invention comprise mixtures ofa volatile ammonium salt, a copper salt, and a combustible carrier material, with or without an inert coloring material.
Amongthe ammonium compounds, the one most suit- Example I Asuitable niixture'may'consist of the following:
Percent by weight Ammonium chloride 4050 Copper'sulfate 5-10 Wood 'fiour 3.0 40
Cupric-chloride maybe substituted for the coppersulfate. The wood flour is preferably about mesh in size, as is the copper sulfate, while the ammonium may be about 20 mesh.
Percent by weight 100 mesh woodflour 39 1O0 mesh copper sulfate monohydrate 7.0 20 mesh ammonium chloride 49 100 mesh iron oxide (FezOs) 5 0 enough of this material used to keep it from being in the form of a free running powder.
Instead of cupric chloride, cuprous chloride, copper of finely ground as spacing agents to avoid too intimate contact between the ammonium halide and the copper compound, for if this were permitted to take place, the mixture might cake and harden up. If the reddish color of the iron oxide should not be deemed desirable, other minerals such as chromium oxide (green), chromates (yellow), ochre (brown), or a blue pigment, or any suitable color lake may be used.
The compositions of the present invention may be employed in a number of different ways. They may be sprinkled on top of the fire in a coal-fired furnace or boiler. They may be blown into the space above or behind the fire, such as into the firebox, lines or passages which the combustion gases traverse on their way to the chimney. They may be introduced at definite intervals, say every four, six, eight, twelve, or twenty-four hours, or sma quantities may be introduced at shorter intervals. The introduction may be at several points in the boiler setting at the same time. The amount used depends entirely upon the size of the installation which is to be treated.
After the composition has been introduced, preferably during a period when the draft in the furnace is somewhat diminished, the draft should be increased so that sufficient oxygen may be available to burn up the carbon (soot) deposits which have accumulated'on the lines, walls, on the water-tubes of a boiler, or in the fire tubes thereof. It required some of the composition can be introduced into the back reaches of a boiler setting, so as to treat that portion and perhaps also some of the chimney surfaces themselves.
It "appears quite probable that both the NHs and HCl components of the ammonium chloride, as well as the copper compounds contribute to the disintegrating action of the composition on the slag and soot deposits. Experience has shown that even very tightly adhering slag deposits become, as it were, rotted, porous and weakened by the action of the constituents of the composition, and hence either drop off under their own weight or are readily dislodged by suitable tools, by tube cleaners or blowers, and the like.
For the cleaning of a 500 H. P. steam boiler, it suffices to throw about 3 to 4 pounds of one of the above mixtures onto the fire. The volatilization of the constituents and the burning of the carrier furnish a vapor or fume that serves to carry them into the fines and tubes containing the sootand scale deposits, where they act as catalysts to facilitate the combustion of the carbon or soot, lowering its ignition temperature about by 300 to 400 F.
The composition comprises a volatile and easily dissociated material in the form of ammonium chloride,
which very readily dissociates, at high temperatures, into free hydrochloric acid gas (HCl) and free ammonia gas (NI-I3). The copper sulfate, probably by reaction with the halogen component of the ammonium salt, forms a volatile copper compound which attacks the mineral constituents of the ash and scale, thereby assisting in loosening it from its adherence to the metallic and brick surfaces of the fiues, walls, tubes and chimneys.
When used in furnace or boiler installations fired by means of oil or gas, the mixture may advantageously be injected at or close to the point of combustion. The combustible ingredient of the composition, such as the wood flour, will'furnish additional heat as the result of its own combustion; also acting as a physical carrier for the inorganic constituents until they attain a temperature sufficiently high to cause them to react and/or volatilize. As the vapors liberated from the composition reach the cooler portions of the boiler, fines, etc., they tend to disintegrate the slag and eliminate the fly ash. The slag becomes disintegrated while the ignition temperature of the carbonaceous material'in the soot is-lowered so that it will ignite and burn up. The local areas of heat thus produced will further aid in the loosening and breaking up of the slag.
A composition which will start to volatilize at the temperature of boiling water, for instance 212 F., or C., is particularly useful, as such volatility is of extreme importance. Thus when applied to or at any designated area the material will instantly volatilize and commence its action upon the surface of which it is applied almost immediately. it has been found that compounds containing sodium chloride, such as have been used in the prior art, cannot be applied in this manner. In the first place they have a density of over 1 so that when injected into the furnace or combustion chamber they immediately fall onto the floor or upon the grate. Moreover, such volatility as they do possess is a rather slow process making their application at specific areas substantially impossible;
in fact all of such types of compounds hitherto used for the present purpose have been thrown upon the grate where the temperature is hottest so as to effect volatiliz'ation of the sodium chloride contents thereof which then was intended to be carried to different places and regions of the boiler and boiler setting by the natural draft of the furnace.
Thus, however, treatment of specific areas in the boiler was impossible under these conditions. Such compounds of the prior art, because of their low volatility, can reach only a very small area, and while some good may be accomplished an over-all treatment of the entire area is impossible.
According to the present invention, however, a composition is used which is of such a physical structure that the treatment of any specific spots or areas in a boiler will be under the absolute control of the operator.
In the operation of a boiler plant using coal or oil as a fuel a number of problems arise, namely as the result of the deposition of the by-products of combustion in the combustion chamber, the superheater bank tubes and the back passes of the boiler.
The particular problems which are likely to be encountered, and which require elimination because of their deleterious effect upon the efficiency of the boiler, are as follows:
Fly ash.-Fly ash is a fine powdered ash which is carried through the different passes of a boiler, becoming deposited in all of the passages as a result of the decrease in the velocity of the air and combustion gases in their passage through the combustion zone and the back passes of the boiler. It is particularly liable to deposit in the breech of the stack and also on the economizer; in fact it often deposits so heavily upon the latter as to make it temporarily useless. By using the compound of the present invention the fly ash will be broken up into such a fine dust that it will remain suspended and thus pass through all the passes of the boiler to be eliminated out of the top of the stack. As a result of this, both the breeching and economizer remain free of fly ash so that the passage of the air and combustion gases will be unimpeded.
This is a very important feature of the action of the compound of the present invention, and so far as the inventor is aware, no other compound has ever approached the present compound in its efficiency for this type of treatment. As a result of its use the fly ash is reduced to a minimum, the passage of air through the boiler is unimpeded so that the boiler may remain in active operation two, three or even four times as long as the usual time without the necessity of shutting it down and cleani V i there is a fan which produces an induced draft, this being used in all cases where good combustion and forced draft are applicable. It is quite important that such a fan be carefully balanced so'that it will not vibrate or get out of alignment, because it is evident that when the fan once gets out ofbalance itcan become uselessand even cause severe darnage.
It is one of the faults of prior art compounds which are based primarily upon sodium chloride, that the latter, due to its lack of volatility, will, even-after having been volatilized on the grate, subsequently condense upon and adhere to the fan blades, with'the result that the. fan gets out-of balance. This, however, cannotoccur when using the compounds of the present invention, because the material is entirely volatile and will pass completely through all of the passes as well as the fan without leaving a harmful deposit;
Slag dep0sits.,D'epending upon thetype of coal burned, more or less slag becomes deposited on the tubes, walls, super-heater banks and other parts of the combustion chamber. This is common in all types of boilers, the quality of the coal being a primary factor. The slag or fusion point of the coal ash is variable; some coals have an ash which is readily fusible while other coals have an ash which fuses at a comparatively high temperature. However, no furnace or combustion chamber will long remain free of slag, as slagging will take place to a greater or less degree. The accumulation of slag is a serious matter; it leads to the spalling of the bricks; it hangs on the tubes, putting a great strain on them by the sheer weight of the deposits which hang in the form of stalacities in the combustion chamber. If such a mass should break off it will sometimes even break the grates of the boiler. The formation of slag on the superheater steam temperature may drop as much as several hundred degrees if the accumulation of slag is heavy.
The use of the compounds of the prior art containing sodium chloride instead of being helpful actually increases the amount of slag deposit by reason of the fact that the compound formed, which now will contain sodium, will have a greater degree of fusibility; moreover compounds containing sodium chloride are not efi'icient in disintegrating slag deposits. As a matter of fact they tend to make them denser and therefore hasten the time when the boiler has to be shut down for repairs. On the other hand the use of a compound which contains materials which are practically 100% volatile eliminates the danger of accumulating slag deposits and has proven to be so elficient tacked, rendered porous, and will become loose and friable so that they may easily be brushed off or blown ofi by means of an air jet or steam jet. It has been definitely demonstrated that even hard dense slag is attacked and rendered soft, loose and friable by use of the compound of the present invention; no matter how long the deposit may have accumulated or how dense it may have become, it will become loose and porous by this treatment.
This leads to an important consideration, namely how long can a boiler carrying soot and carbon deposits as well as slag be left in service? Most engineers do not care to keep a boiler in service for more than three months at a time, for experience has taught them that this is about the time that scale, slag and fly ash deposits have accumulated to such an extent that the boiler will be no longer operating at an efficient rate. It therefore at that time becomes necessary to draw the fires, cool down the boiler and open it up for inspection. This will take the better part of a week while quite frequently another week or two is spent in chiseling oi the accumulated slag deposits from the walls and tubes. Often the old brick work has been so badly damaged that it has to be replaced by new fire brick, particularly at the points where spalling has taken place or where the fire brick has been attacked.
The superheater banks and the economizer also have to be cleaned, and the fly ash deposits removed. All of be desired, and several thousands of dollars a-zyear can be saved in'operatm'gexpenses if. th'e boiler canbeial ash, soot and other deposits. Dependingnpon the amount of water evaporated 'per day, asmuch as $20.00 peizday can be saved when the' superheater temperatures are .kept at their predetermined .point. All these'desirable effects can be attained by the use of the compound ofthewpresent invention. Moreover, the amount of compound used is also important. It has been found that under average operating conditions the use of as little as 1 pound of the compound per H. P. per day will keep the boiler clean and the operation eflicient.
It is to be understood that the application of the compound is not limited to just the areas close to the tire box or grate for it may be used in any part of the boiler where conditions indicate that a deposit exists or is forming and operator.
Soot and carbomAoot and carbon deposits are formed on certain areas in all boilers, even those operating on oil. Ordinarily this is eliminated by the use of so-called soot blowers. Tthis procedure is usually done at night because of the fact that the clouds of black sooty carbonaceous material blown out of the boiler cannot be seen, but it nevertheless escapes from the boiler and settles upon the adjacent area. The use of the compound of the present invention will get rid of all soot and carbon deposits by reason of the catalytic action of the vapors produced by the volatilization of the material in the present compound which cause the carbon and soot to ignite at a fairly low temperature and thus to burn away to form carbon dioxide which freely escapes in the form of a gas. The substantially complete volatilization of the present compound allows this action to go on and therefore serves to eliminate soot and carbon residues; as a result, therefore, boilers using this material do not have to be cleaned with soot blowers, so that they will now no longer be a nuisance in the neighborhood.
From the further description hereinbelow the nature of the present compound and the reason for its efiiciency will be more adequately disclosed.
During the latter stages of the action of the composition, suflicient draft should be available to supply the oxygen required for the elfective combustion of the soot.
should be on the order of 23,000 cubic feet.
The combustible carrier, by being very finely divided, will of course also be air borne and by its own combustion will generate heat which serves further to increase the volatilization of the volatile constituents of the mixture. Inasmuch as the carrier has little ash of its own, such as in the case of wood flour, or ground corn cobs, or starches, it will of course in no way cause any deposits of its own. In other words, the entire mixture introduced into the furnace eventually passes out through the stack, together with the material which it is desired to eliminate, thus leaving the furnace walls, tubes, superheater and the various reaches of the boiler in clean and serviceable condition, so as to obtain the best possible heat transfer between the heat of the combustion gases and the heat absorbing metal parts of the boiler.
This is even advantageous so far as the walls of the boiler setting are concerned, because it is well known that a bright clean surface will reflect heat better so that a better effect of, radiation fromsthe walls of the heat absorbing surfaces it attained.
It will be obvious that modifications in the proportions of the composition may be made, and it is the intention to include such 'modifications within the purview and scope of the present invention.
I claim:
A fly ash, slag, soot and carbon eliminator which is extremely light, has a density of not over 0.40, is capable of being air borne and which is extremely volatile in the combustion chamber and back passes of a boiler, comprising from about 40% to 50% by weight of ammonium chloride, about %'to of copper sulfate, about to of wood flour, and enough mineral coloring matter to make References Cited in the file of this patent UNITED STATES PATENTS OTHER REFERENCES Removal of Soot from Furnaces and'Flues by the Use of Salts or Compounds, U.'S. Dept of Commerce, Bureau of Mines, Bulletin 360, pages 3, 8-10, 23-25, 29.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US434349A US2777761A (en) | 1954-06-03 | 1954-06-03 | Composition for eliminating slag, soot, and fly ash |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US434349A US2777761A (en) | 1954-06-03 | 1954-06-03 | Composition for eliminating slag, soot, and fly ash |
Publications (1)
Publication Number | Publication Date |
---|---|
US2777761A true US2777761A (en) | 1957-01-15 |
Family
ID=23723863
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US434349A Expired - Lifetime US2777761A (en) | 1954-06-03 | 1954-06-03 | Composition for eliminating slag, soot, and fly ash |
Country Status (1)
Country | Link |
---|---|
US (1) | US2777761A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4190421A (en) * | 1978-07-17 | 1980-02-26 | Chemed Corporation | Fireside treating compositions |
US4481010A (en) * | 1983-09-22 | 1984-11-06 | Hercules Chemical Company, Inc. | Non-corrosive creosote and soot removing composition |
US4571247A (en) * | 1984-03-19 | 1986-02-18 | Cavallino S.N.C. Prodotti Chimici | Product in tablet form for use in the chemical elimination of soot from chimneys and smoke ducts |
WO1986007602A1 (en) * | 1985-06-20 | 1986-12-31 | Sparol International Aps | A powder additive for use in the combustion of solid materials, and the use of the powder additive |
FR2749855A1 (en) * | 1996-10-10 | 1997-12-19 | Eurexim | New solid fuel agents for the decomposition of soot and oily deposits in smoke flues |
FR2800745A1 (en) * | 1999-11-10 | 2001-05-11 | Philippe Madamour | Solid composition for destroying soot and tar, useful for cleaning chimneys, comprises active agent, plant waste and binder |
WO2002046337A1 (en) * | 2000-12-07 | 2002-06-13 | Philippe Madamour | Solid agent for eliminating soot and in particular tars, and method for making same and uses thereof |
US20040168366A1 (en) * | 2003-02-28 | 2004-09-02 | Clark Schaefer | Creosote and soot destroying fire log |
US20090071068A1 (en) * | 2007-09-14 | 2009-03-19 | John Cook | Method for reducing flammable creosote and other organic deposits in fireboxes |
EP2434003A1 (en) | 2010-09-23 | 2012-03-28 | Chembo S.A. | Solid composition for chemical chimney-cleaning |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US523117A (en) * | 1894-07-17 | Soot-preventing composition | ||
GB189709876A (en) * | 1897-04-20 | 1898-04-16 | William Samuel Frost | An Improved Method for Cleaning Chimneys and for Extinguishing Fires in the same. |
GB189813711A (en) * | 1898-06-20 | 1899-04-22 | Thomas Voile | New or Improved Means for Destroying Soot in Chimneys. |
GB189826736A (en) * | 1898-12-19 | 1899-12-02 | Charles Ebenezer Challis | Composition for Removing Soot and Scale from Chimneys, Flues, and the like. |
-
1954
- 1954-06-03 US US434349A patent/US2777761A/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US523117A (en) * | 1894-07-17 | Soot-preventing composition | ||
GB189709876A (en) * | 1897-04-20 | 1898-04-16 | William Samuel Frost | An Improved Method for Cleaning Chimneys and for Extinguishing Fires in the same. |
GB189813711A (en) * | 1898-06-20 | 1899-04-22 | Thomas Voile | New or Improved Means for Destroying Soot in Chimneys. |
GB189826736A (en) * | 1898-12-19 | 1899-12-02 | Charles Ebenezer Challis | Composition for Removing Soot and Scale from Chimneys, Flues, and the like. |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4190421A (en) * | 1978-07-17 | 1980-02-26 | Chemed Corporation | Fireside treating compositions |
US4481010A (en) * | 1983-09-22 | 1984-11-06 | Hercules Chemical Company, Inc. | Non-corrosive creosote and soot removing composition |
US4571247A (en) * | 1984-03-19 | 1986-02-18 | Cavallino S.N.C. Prodotti Chimici | Product in tablet form for use in the chemical elimination of soot from chimneys and smoke ducts |
WO1986007602A1 (en) * | 1985-06-20 | 1986-12-31 | Sparol International Aps | A powder additive for use in the combustion of solid materials, and the use of the powder additive |
US5882365A (en) * | 1996-10-10 | 1999-03-16 | Eurexim | Soot disaggregating combustible agent |
EP0837121A1 (en) * | 1996-10-10 | 1998-04-22 | Eurexim | Solid fuel for destroying soot and tars, method for making the same, and use thereof |
FR2749855A1 (en) * | 1996-10-10 | 1997-12-19 | Eurexim | New solid fuel agents for the decomposition of soot and oily deposits in smoke flues |
FR2800745A1 (en) * | 1999-11-10 | 2001-05-11 | Philippe Madamour | Solid composition for destroying soot and tar, useful for cleaning chimneys, comprises active agent, plant waste and binder |
WO2002046337A1 (en) * | 2000-12-07 | 2002-06-13 | Philippe Madamour | Solid agent for eliminating soot and in particular tars, and method for making same and uses thereof |
US20040088912A1 (en) * | 2000-12-07 | 2004-05-13 | Philippe Madamour | Solid agent for eliminating soot and in particular tars, and method for making same and uses thereof |
US20040168366A1 (en) * | 2003-02-28 | 2004-09-02 | Clark Schaefer | Creosote and soot destroying fire log |
US7540890B2 (en) | 2003-02-28 | 2009-06-02 | Clark Schaefer | Creosote and soot destroying fire log |
US20090071068A1 (en) * | 2007-09-14 | 2009-03-19 | John Cook | Method for reducing flammable creosote and other organic deposits in fireboxes |
EP2434003A1 (en) | 2010-09-23 | 2012-03-28 | Chembo S.A. | Solid composition for chemical chimney-cleaning |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2777761A (en) | Composition for eliminating slag, soot, and fly ash | |
US2059388A (en) | Treatment for improving bituminous coal | |
US4842617A (en) | Combustion control by addition of magnesium compounds of particular particle sizes | |
US3004836A (en) | Reduction of slag formation in coalfired furnaces, boilers and the like | |
US4706579A (en) | Method of reducing fireside deposition from the combustion of solid fuels | |
CA1169650A (en) | Vermiculite as a deposit modifier in coal fired boilers | |
US3738819A (en) | Method of using combustion adjuvant | |
FI81375B (en) | Finely divided additive for use when combusting solid substances | |
US4190421A (en) | Fireside treating compositions | |
CN206037066U (en) | It contains alkali organic waste liquid incineration disposal waste heat recovery system to contain salt | |
US3630696A (en) | Combustion adjuvant | |
CN101955818B (en) | Coke-removing and soot-cleaning combustion improver for boiler | |
US3628925A (en) | Combustion adjuvant | |
AU594867B2 (en) | Method of burning, in particular, salt-containing brown coal | |
EP0058086B1 (en) | Method for the prevention of deposits on or the removal of deposits from heating and ancillary surfaces | |
US2843200A (en) | Fuel oils | |
US2610112A (en) | Soot removal compositions | |
KR100686361B1 (en) | Cleaning composition for fuel apparatus | |
CN112664953A (en) | Circulating fluidized bed incineration boiler for burning solid waste | |
JPS6064118A (en) | Combustion method of sludge containing low-melting substance | |
US1609059A (en) | Soot-destroyer composition | |
CA1059835A (en) | Furnace design for pulverized coal and stoker firing | |
NL8201903A (en) | METHOD FOR REMOVING FLY GAS IN OVEN MORE EASILY. | |
Murphy Jr et al. | Fireside deposits on steam generators minimized through humidification of combustion air | |
EP0130065A1 (en) | Improvements in and relating to combustion |