EP1597413A1 - Traitement non corrosif destine a ameliorer la combustion de charbon pulverise mis sous pression ou non - Google Patents

Traitement non corrosif destine a ameliorer la combustion de charbon pulverise mis sous pression ou non

Info

Publication number
EP1597413A1
EP1597413A1 EP04705247A EP04705247A EP1597413A1 EP 1597413 A1 EP1597413 A1 EP 1597413A1 EP 04705247 A EP04705247 A EP 04705247A EP 04705247 A EP04705247 A EP 04705247A EP 1597413 A1 EP1597413 A1 EP 1597413A1
Authority
EP
European Patent Office
Prior art keywords
recited
aqueous solution
copper
amount
coal
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.)
Withdrawn
Application number
EP04705247A
Other languages
German (de)
English (en)
Inventor
Nicholas Robert Blandford
Libardo A. Perez
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
General Electric Co
Original Assignee
General Electric Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by General Electric Co filed Critical General Electric Co
Publication of EP1597413A1 publication Critical patent/EP1597413A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L5/00Solid fuels
    • C10L5/02Solid fuels such as briquettes consisting mainly of carbonaceous materials of mineral or non-mineral origin
    • C10L5/34Other details of the shaped fuels, e.g. briquettes
    • C10L5/36Shape
    • C10L5/366Powders
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L9/00Treating solid fuels to improve their combustion
    • C10L9/10Treating solid fuels to improve their combustion by using additives
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21BMANUFACTURE OF IRON OR STEEL
    • C21B5/00Making pig-iron in the blast furnace
    • C21B5/001Injecting additional fuel or reducing agents
    • C21B5/003Injection of pulverulent coal
    • C21B5/004Injection of slurries
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F11/00Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/02Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in air or gases by adding vapour phase inhibitors

Definitions

  • the invention pertains to methods and compositions for inhibiting corrosion of metal surfaces in contact with a furnace.
  • iron bearing materials including iron ore, sinter, scrap, or other iron source along with a fuel, generally coke, and a flux, limestone, or dolomite are charged into the blast furnace from the top.
  • the blast furnace burns part of the fuel to produce heat for melting the iron ore and the balance of the fuel is utilized for reducing the iron and its combination with carbon.
  • the charge. in a typical furnace, per ton of pig iron produced, is about 1.7 tons of ore or other iron bearing materials, 0.5-0.65 tons of coke or other fuel, and about 0.25 tons of limestone and/or dolomite. Additionally, from 1.8-2.0 tons of air are blown into the furnace during the process.
  • iron bearing raw materials sinter, iron ore, pellets, etc.
  • fuel coke
  • flux limestone, dolomite, etc.
  • Heated air blast
  • Tuyere stocks are fitted with injection lances through which supplemental fuels (gas, oil, and pulverized coal) are injected.
  • the blast air burns the fuel and facilitates the smelting chemistry that produces iron.
  • Combustion gases from the blast furnace are scrubbed to remove particulate and other noxious gases before being burned in stoves which are used to preheat blast air or in other applications, e.g., coke ovens, boilers, etc.
  • metals such as those disclosed in the '325 patent may be used as combustion catalysts or aids. These are of benefit since they provide the ability to use lower rank coals in the furnace and allow for greater coke replacement by the pulverized coal. Additionally, they help to minimize "coal cloud" and reduce LOI. Lowered slag content, reduced particulate emissions, and higher quality iron are also potential benefits that may be attributed to the use of these catalysts or aids.
  • Copper-based catalysts or combustion aids have become especially popular. However, attendant problems of corrosion have appeared as a result. The problem arises from the corrosion that the product generates on mild steel surfaces that are present in the furnace system in which the combustion catalyst/aid is applied. (As used herein, "furnace” and “furnace systems” refer to ovens, boilers, blast furnaces, or any enclosure in which a fuel is combusted.)
  • the corrosion inhibiting treatment of the invention is blended with a copper combustion catalyst/aid to form a protective film on the mild steel surface in contact with the furnace combustion products.
  • the corrosion inhibiting treatment comprises a blend of a primary aminoalcohol (i.e., having primary amino function) and boric acid or water soluble salt or the acid.
  • a tertiary aminoalcohol i.e., having a tertiary amine function
  • the blend is preferably sprayed onto the pulverized coal in aqueous solution form prior to injection of the coal into the furnace.
  • the treatment may be applied in spray form anywhere in the furnace system including the so-called "fireside” or "cold” ends of the furnace. (See U.S. Patents 4,458,006 and 4,224,180 herein incorporated by reference.)
  • Metal surfaces, such as mild steel surfaces, of a furnace system are effectively treated in accordance with the invention by a corrosion inhibiting treatment comprising a blend of a primary aminoalcohol and boric acid or water soluble salt form thereof.
  • the corrosion inhibiting treatment may comprise a tertiary aminoalcohol.
  • the primary aminoalcohol is 2-aminoethanol and the tertiary aminoalcohol is triethanolamine.
  • the invention has proven to be successful, especially in furnace systems in which pulverized coal is burned as fuel in the presence of a copper catalyst/combustion aid.
  • the corrosion inhibiting treatment is most preferably provided in the form of an aqueous solution.
  • aqueous solution we mean to encompass not only true chemical solutions, but also dispersions, mixtures, and suspensions.
  • the solution may be sprayed directly over the pulverized coal in an amount of about 100 ml to 1 L of aqueous solution per ton of coal. More preferably, the dosage rate is from about 300 ml -IL of aqueous solution per ton pulverized coal.
  • the corrosion inhibiting treatment comprises both the 2-aminoethanol and triethanolamine component.
  • conventional corrosion inhibitors such as water-soluble gluconic acid salts, preferably sodium gluconate, may be incorporated into the corrosion inhibiting treatment.
  • a copper ion source may also be incorporated into the aqueous solution that is to be sprayed over the coal.
  • the invention is also directed to corrosion inhibiting treatment compositions that are adapted for application or spraying onto the fuel in the form of an aqueous solution.
  • the 2-aminoethanol, triethanolamine, and boric acid or salt thereof components may be present in the aqueous solution in the amount of about 1- 10 wt%.
  • Sodium gluconate may also be present in the aqueous solution in an amount of about 1-15 wt%.
  • the copper ion source may be present in such an amount as to provide Cu ++ in an amount of 1-20 wt%.
  • the synergistic blend of 2-aminoethanol, triethanolamine, and borate is not water soluble in the presence of copper.
  • this blend is mixed with the known mild steel corrosion inhibitor, sodium gluconate, the gluconate/"blend" mixture has a high solubility in water even in the presence of copper.
  • compositions in accordance with the invention include:
  • aminoalcohol component(s) and boric acid or salt 1-10 wt% aminoalcohol component(s) and boric acid or salt 1-10 wt%
  • compositions include
  • Cu + ion in aqueous solution Based upon preliminary results, it is preferred to provide the copper ion source, sodium gluconate, 2-aminoethanol, triethanolamine, and boric acid or water soluble salt in a single aqueous solution for spray application over the pulverized coal.
  • Exemplary copper ion sources are copper sulfate pentahydrate and copper II-D- gluconate.
  • the product which is presently preferred for commercial use comprises about 3% actives of a blend of 2-aminoethanol, triethanolamine, and boric acid, along with 4% active sodium gluconate, and 19% actives of copper sulfate pentahydrate along with sufficient water to equal 100% of the total weight of the formulation.
  • the level of copper (as Cu 2+ in EP9587 (4.84%o) was maintained for each new stock formulation prepared.
  • the percentage of surfactant and water and the source of copper ion were the variables manipulated. All blends were prepared based on the weight % of each component. In addition, an 11- day test using undiluted stock solutions was carried out with the better of the two corrosion blends.
  • Example 2 The procedures reported in Example 1 were again performed in conjunction with comparative treatments and treatments in accordance with the invention. Results are shown in Table 2.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Mechanical Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Combustion & Propulsion (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Geology (AREA)
  • Catalysts (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)
  • Detergent Compositions (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)
  • Liquid Carbonaceous Fuels (AREA)

Abstract

L'invention concerne des procédés et des compositions destinés à inhiber la corrosion de surfaces métalliques dans un système de four. Dans aspect de l'invention, du charbon pulvérisé est brûlé comme combustible en présence d'un catalyseur ionique de cuivre/adjuvant de combustion. La corrosion est inhibée dans ces systèmes au moyen d'un mélange d'un aminoalcool primaire tel que le 2-aminoéthanol, d'un aminoalcool tertiaire tel que la triéthanolamine, et d'un acide borique ou d'une forme saline hydrosoluble de cet acide.
EP04705247A 2003-02-19 2004-01-26 Traitement non corrosif destine a ameliorer la combustion de charbon pulverise mis sous pression ou non Withdrawn EP1597413A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US368823 1995-01-05
US10/368,823 US20040159184A1 (en) 2003-02-19 2003-02-19 Non-corrosive treatment to enhance pressurized and non-pressurized pulverized coal combustion
PCT/US2004/002051 WO2004074548A1 (fr) 2003-02-19 2004-01-26 Traitement non corrosif destine a ameliorer la combustion de charbon pulverise mis sous pression ou non

Publications (1)

Publication Number Publication Date
EP1597413A1 true EP1597413A1 (fr) 2005-11-23

Family

ID=32850212

Family Applications (1)

Application Number Title Priority Date Filing Date
EP04705247A Withdrawn EP1597413A1 (fr) 2003-02-19 2004-01-26 Traitement non corrosif destine a ameliorer la combustion de charbon pulverise mis sous pression ou non

Country Status (9)

Country Link
US (3) US20040159184A1 (fr)
EP (1) EP1597413A1 (fr)
JP (1) JP4440919B2 (fr)
KR (1) KR101138658B1 (fr)
CN (1) CN100351430C (fr)
AU (1) AU2004213746B2 (fr)
BR (1) BRPI0407655A (fr)
CA (1) CA2516491C (fr)
WO (1) WO2004074548A1 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101838810B (zh) * 2010-05-18 2012-03-14 深圳市堃琦鑫华科技有限公司 易降解的水溶性熔融金属抗氧化还原剂
TWI704233B (zh) * 2018-10-02 2020-09-11 孫文彬 助燃劑的製備方法及其系統

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US2836566A (en) * 1954-01-27 1958-05-27 Detrex Chem Ind Cleaning composition and method
US3406042A (en) * 1965-12-14 1968-10-15 Cons Edison Co New York Inc Process for corrosion control
US4134729A (en) * 1976-08-12 1979-01-16 Betz Laboratories, Inc. Aqueous solution of sodium aluminate and N-aminoethyl ethanolamine as a cold end additive
US4101293A (en) * 1977-03-30 1978-07-18 Reichhold Chemicals, Inc. Stabilizing emulsifiers
US4293342A (en) * 1978-02-09 1981-10-06 American Can Company Lignosulfonate derivatives
US4208188A (en) * 1978-03-22 1980-06-17 Signet Corporation Consolidation of coal slurry
US4224180A (en) * 1979-10-30 1980-09-23 Betz Laboratories, Inc. Cold end additive compositions
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US4732572A (en) * 1985-10-03 1988-03-22 Westvaco Corporation Amine salts of sulfomethylated lignin
JPS62241993A (ja) * 1986-04-15 1987-10-22 Mitsui Mining Co Ltd 石炭−メタノ−ルスラリ−およびその製造方法
FR2621175B1 (fr) * 1987-09-29 1989-12-01 Accumulateurs Fixes Generateur electrochimique amorcable mettant en oeuvre des couples lithium/oxyhalogenure
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JPH07188954A (ja) * 1993-12-28 1995-07-25 Ishizuka Glass Co Ltd 水溶性防錆剤
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WO1999035215A2 (fr) * 1998-01-12 1999-07-15 Deborah Wenzel Composition additive egalement utilisee comme composition combustible contenant des alcools hydrosolubles
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JP4842420B2 (ja) * 1999-09-28 2011-12-21 トヨタ自動車株式会社 冷却液、冷却液の封入方法および冷却システム
JP3402365B2 (ja) 2000-06-28 2003-05-06 日本電気株式会社 防食剤
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Also Published As

Publication number Publication date
US20090253085A1 (en) 2009-10-08
CN100351430C (zh) 2007-11-28
US20040159184A1 (en) 2004-08-19
WO2004074548A1 (fr) 2004-09-02
KR20050102123A (ko) 2005-10-25
JP2006518419A (ja) 2006-08-10
KR101138658B1 (ko) 2012-04-19
CN1764741A (zh) 2006-04-26
AU2004213746A1 (en) 2004-09-02
BRPI0407655A (pt) 2006-02-21
CA2516491A1 (fr) 2004-09-02
US20070033864A1 (en) 2007-02-15
JP4440919B2 (ja) 2010-03-24
AU2004213746B2 (en) 2009-05-07
CA2516491C (fr) 2013-07-09

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