NO144619B - PROCEDURE AND PREPARATION FOR AA FIGHT AGAINST DISPOSAL BUILDING IN GAS WASHERS - Google Patents
PROCEDURE AND PREPARATION FOR AA FIGHT AGAINST DISPOSAL BUILDING IN GAS WASHERS Download PDFInfo
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- NO144619B NO144619B NO764352A NO764352A NO144619B NO 144619 B NO144619 B NO 144619B NO 764352 A NO764352 A NO 764352A NO 764352 A NO764352 A NO 764352A NO 144619 B NO144619 B NO 144619B
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- polymer
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- molecular weight
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- 238000002360 preparation method Methods 0.000 title claims description 11
- 238000000034 method Methods 0.000 title claims description 8
- 229920000642 polymer Polymers 0.000 claims description 15
- 239000003112 inhibitor Substances 0.000 claims description 13
- 229920001577 copolymer Polymers 0.000 claims description 8
- ZHCGVAXFRLLEFW-UHFFFAOYSA-N 2-methyl-3-(prop-2-enoylamino)propane-1-sulfonic acid Chemical compound OS(=O)(=O)CC(C)CNC(=O)C=C ZHCGVAXFRLLEFW-UHFFFAOYSA-N 0.000 claims description 6
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 229920002401 polyacrylamide Polymers 0.000 claims description 5
- 238000005201 scrubbing Methods 0.000 claims description 5
- 229920000388 Polyphosphate Polymers 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 150000001340 alkali metals Chemical class 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 229910021645 metal ion Inorganic materials 0.000 claims description 3
- 239000001205 polyphosphate Substances 0.000 claims description 3
- 235000011176 polyphosphates Nutrition 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims 2
- 239000007789 gas Substances 0.000 description 23
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 18
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 13
- 238000005406 washing Methods 0.000 description 11
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 10
- 229910052742 iron Inorganic materials 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000000428 dust Substances 0.000 description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 229910000019 calcium carbonate Inorganic materials 0.000 description 5
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000002893 slag Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 235000011941 Tilia x europaea Nutrition 0.000 description 3
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 3
- 229910001634 calcium fluoride Inorganic materials 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 239000000571 coke Substances 0.000 description 3
- 239000004571 lime Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- YDONNITUKPKTIG-UHFFFAOYSA-N [Nitrilotris(methylene)]trisphosphonic acid Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CP(O)(O)=O YDONNITUKPKTIG-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000010459 dolomite Substances 0.000 description 2
- 229910000514 dolomite Inorganic materials 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 229920006158 high molecular weight polymer Polymers 0.000 description 2
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000011236 particulate material Substances 0.000 description 2
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000005200 wet scrubbing Methods 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 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
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004939 coking Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003546 flue gas Substances 0.000 description 1
- 239000010436 fluorite Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- LDHBWEYLDHLIBQ-UHFFFAOYSA-M iron(3+);oxygen(2-);hydroxide;hydrate Chemical compound O.[OH-].[O-2].[Fe+3] LDHBWEYLDHLIBQ-UHFFFAOYSA-M 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 1
- 235000019830 sodium polyphosphate Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F5/00—Softening water; Preventing scale; Adding scale preventatives or scale removers to water, e.g. adding sequestering agents
- C02F5/08—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents
- C02F5/10—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances
- C02F5/14—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances containing phosphorus
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F5/00—Softening water; Preventing scale; Adding scale preventatives or scale removers to water, e.g. adding sequestering agents
- C02F5/08—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents
- C02F5/10—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances
- C02F5/14—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances containing phosphorus
- C02F5/145—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances containing phosphorus combined with inorganic substances
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Hydrology & Water Resources (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Inorganic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Treating Waste Gases (AREA)
- Detergent Compositions (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Description
Foreliggende oppfinnelse angår en'fremgangsmåte og et•prepa-rat for å bekjempe avsetningsoppbygning i gassvaskere. The present invention relates to a method and a preparation for combating deposit build-up in gas scrubbers.
I løpet av de siste år har antallet av våtvaskesystemer installert for å fjerne gass- og partikkelformig materiale fra avfallsskorstensgasser øket voldsomt. Ytterligere slike systemer er nu på tegnebordet. Disse våtgassvaskere er blitt anvendt for å klare avløpet fra kjeleskorstener, forbrenningsskorstener, kalkovner, støperier, masovner, basiske oxygenovner (BOF), Siemens-Martin-enheter, koksanlegg, cellulose-gjenvinningskjeler, anlegg for fremstilling av kjæledyrfor, elektriske ovner (stål og aluminium), smelteovner, asfaltanlegg og mange andre. In recent years, the number of wet scrubbing systems installed to remove gaseous and particulate material from waste stack gases has increased dramatically. Further such systems are now on the drawing board. These wet gas scrubbers have been used to clean the effluent from boiler chimneys, incinerators, lime kilns, foundries, blast furnaces, basic oxygen furnaces (BOF), Siemens-Martin units, coking plants, cellulosic recovery boilers, pet food manufacturing plants, electric furnaces (steel and aluminum ), smelters, asphalt plants and many others.
Et av de viktigste trekk ved et gassvaskesystem er kontakt-kammeret, anordningen som anvendes for effektiv overføring av gassformig og/eller partikkelformig materiale fra gassen til vann-fasen. De fleste våtvaskesystemer involverer en venturi, et pakket lag, en hullplate, et dusjkammer eller et turbulent lag. Noen systemer anvender endog to kontaktkammere i serie, f.eks. en venturi fulgt av et dusjkammer. One of the most important features of a gas washing system is the contact chamber, the device used for the efficient transfer of gaseous and/or particulate material from the gas to the water phase. Most wet scrubbing systems involve a venturi, packed bed, perforated plate, shower chamber, or turbulent bed. Some systems even use two contact chambers in series, e.g. a venturi followed by a shower chamber.
Venturi- eller hullplatevaskere er i alminnelighet mere effektive til å fjerne partikkelformig materiale mens pakkede lag, turbulente lag og dusjkammere vanligvis er mere effektive til å fjerne gassformige bestanddeler som SO,, eller HF. Venturi or perforated plate scrubbers are generally more effective at removing particulate matter, while packed beds, turbulent beds, and shower chambers are generally more effective at removing gaseous constituents such as SO,, or HF.
Foreliggende oppfinnelse angår spesielt de gassvaskesystemer hvor skall- og avsetningsproblemer på grunn av uoppløse-lig calciumcarbonat , calciumf luorid, jernoxyd (Fe^^) » silicium-oxyd, manganoxyd, jernmalrastøv og slaggstøv foreligger. Det problem som foreliggende oppfinnelse reduserer, er det som foreligger i gassvaskesystemer for masovnoperasjoner hvor jernmalm overføres eller bearbeides til jern med et høyt carboninnhold. The present invention relates in particular to gas washing systems where scale and deposition problems due to insoluble calcium carbonate, calcium fluoride, iron oxide (Fe^^) » silicon oxide, manganese oxide, iron mill dust and slag dust are present. The problem that the present invention reduces is that which exists in gas washing systems for mass operations where iron ore is transferred or processed into iron with a high carbon content.
For å sikre en fullstendig forståelse av problemet som foreliggende oppfinnelse angår, gies i det følgende en kort beskrivelse av en masovnoperasjon. In order to ensure a complete understanding of the problem to which the present invention relates, a brief description of a mass operation is given below.
Ved fremstilling av jern mates jernmalm sammen med andre bestanddeler som dolomit inn gjennom toppen av en masovn som fyres med koks. En luftstrøm blåses oppad fra bunnen av ovnen gjennom de senere smeltede materialer. Carbonet fra koksen reduserer jernmalmen (^ Fe^ O^) til metallisk jern. Det smeltede jern tappes fra bunnen av ovnen mens slaggen tappes fra midten av ovnen. Biproduktet fra carbonreduksjonen er selvsagt en kombinasjon av carbondioxyd og carbonmonoxyd som reagerer med det tilstedeværende calcium under dannelse av den brysomme skalldanner, calciumcarbonat og andre faste stoffer som leire, slagg, støv, etc. In the production of iron, iron ore is fed together with other components such as dolomite through the top of a blast furnace that is fired with coke. An air stream is blown upwards from the bottom of the furnace through the later melted materials. The carbon from the coke reduces the iron ore (^ Fe^ O^) to metallic iron. The molten iron is drained from the bottom of the furnace while the slag is drained from the center of the furnace. The by-product from the carbon reduction is of course a combination of carbon dioxide and carbon monoxide which reacts with the calcium present to form the troublesome scale former, calcium carbonate and other solid substances such as clay, slag, dust, etc.
Som det vil forståes, bidrar luftstrømmen som blåses oppad, betraktelig til forurensningsinnholdet av avgassen, og legger så-ledes en stor byrde på vaskesystemet. Det partikkelformige innhold i vaskemediet varierer fra 1.000 til 2.000 ppm på grunn av part ikke1innholdet i skorstensgassen. As will be understood, the air flow which is blown upwards contributes considerably to the pollution content of the exhaust gas, and thus places a great burden on the washing system. The particulate content in the washing medium varies from 1,000 to 2,000 ppm due to the particulate content in the flue gas.
Vaskerne som anvendes for rensning av masovngass, er ofte av venturikonstruksjonen og behandler avgassene fra ovnen. Disse gasser inneholder betraktelige mengder jernoxyd, hvis fine par-tikkelstørrelse tillater den å medføres av gasstrømmen. Dessuten kan koksstøv være tilstede i mindre grad og i noen grad partikkelformig slaggmateriale som anvendes som silikater og ubrukt dolomit. Jernoxydet har vært utsatt for høye temperaturer i ovnen og kan derfor være i en sintret form med lav overflateaktivitet. Dets fine partikkelstørrelse forårsaker imidlertid avsetningsproblemer i vaskerne og utførselsledningene. The scrubbers used to clean blast furnace gas are often of the venturi design and process the exhaust gases from the furnace. These gases contain considerable amounts of iron oxide, whose fine particle size allows it to be entrained by the gas stream. In addition, coke dust may be present to a lesser extent and to some extent particulate slag material which is used as silicates and unused dolomite. The iron oxide has been exposed to high temperatures in the furnace and may therefore be in a sintered form with low surface activity. However, its fine particle size causes deposition problems in the scrubbers and discharge lines.
Et annet eksempel på et operativt system er en basisk oxygenovn (BOF) hvori ovnen mottar smeltet metall fra masovnen foruten skrap, forskjellige legeringer for å oppfylle spesifikasjonene, Another example of an operational system is a basic oxygen furnace (BOF) in which the furnace receives molten metal from the blast furnace in addition to scrap, various alloys to meet specifications,
og kalk og flusspat som flussmiddel. Oxygen innføres gjennom en lanse for å fjerne forurensninger. Oxygenblesten kan frigjøre 4,4 tonn støv pr. 220 tonn sats. Dette støv må gjenvinnes fra-utløpsgassen. Støvet består av jernoxyd, kalk og fluorid. and lime and fluorspar as a flux. Oxygen is introduced through a lance to remove contaminants. The oxygen blast can release 4.4 tonnes of dust per 220 ton rate. This dust must be recovered from the exhaust gas. The dust consists of iron oxide, lime and fluoride.
Disse partikkelholdige og oppløselige gasser fjernes fra avgassen i en våt gassvasker. I vaskevannet forenes jernoxydet, calciumfluoridet og calciumcarbonatet til å bevirke stor avsetningsoppbygning på vaskesystemveggene, hvilket fører til ineffektiv vaskeoperasjon og høye vedlikeholdsomkostninger. These particulate and soluble gases are removed from the exhaust gas in a wet gas scrubber. In the washing water, the iron oxide, calcium fluoride and calcium carbonate combine to cause a large build-up of deposits on the washing system walls, which leads to inefficient washing operations and high maintenance costs.
Ved tidligere kjente metoder som metoden angitt i U.S. patent 3.880.620, anvendes skallavsetningsinhibitorer, dvs. uorganiske og organiske fosfater; og lavmolekylære polymere dispersjons-midler. Denne løsning har ikke vært helt vellykket til å forhindre avsetning og har ført til økede behandlingsomkostninger og hyppige nedstengninger for mekanisk rengjøring. In previously known methods such as the method set forth in U.S. patent 3,880,620, shell deposition inhibitors are used, i.e. inorganic and organic phosphates; and low molecular weight polymeric dispersants. This solution has not been entirely successful in preventing deposition and has led to increased treatment costs and frequent shutdowns for mechanical cleaning.
Det er følgelig et mål ved foreliggende oppfinnelse å frem-skaffe en fremgangsmåte og et preparat for effektivt å forhindre avsetning i gassvaskere, og som er økonomiske og nedsetter til et minimum hyppigheten av mekanisk rengjøring av gassvaskeutstyr, og som er effektive over et bredt pH-område. It is therefore an aim of the present invention to provide a method and a preparation for effectively preventing deposits in gas scrubbers, which are economical and reduce to a minimum the frequency of mechanical cleaning of gas scrubber equipment, and which are effective over a wide pH range area.
Disse og andre mål ved foreliggende oppfinnelse oppnåes ved fremgangsmåten og preparatet ifølge oppfinnelsen hvori fra 0,01 til 100 ppm aktive bestanddeler, fortrinnsvis fra 0,1 til 10 ppm aktive bestanddeler, av'et preparat omfattende en skallinhibitor og en høymolekylær polymer opprettholdes i det vandige vaskemedium. Forholdet av høymolekylær polymer til skallinhibitor kan være fra 1:10 til 10:1, fortrinnsvis fra 1:5 til 5:1,.i vekt. These and other objectives of the present invention are achieved by the method and the preparation according to the invention in which from 0.01 to 100 ppm active ingredients, preferably from 0.1 to 10 ppm active ingredients, of a preparation comprising a shell inhibitor and a high molecular weight polymer is maintained in the aqueous washing medium. The ratio of high molecular polymer to shell inhibitor can be from 1:10 to 10:1, preferably from 1:5 to 5:1, by weight.
Passende terskel-skallinhibitorer omfatter fosfonater med den generelle formel: hvor R er Suitable threshold-shell inhibitors include phosphonates of the general formula: where R is
M er H, NH^, alkalimetall eller kombinasjoner derav; M is H, NH 3 , alkali metal or combinations thereof;
n er 0 til 6; og n is 0 to 6; and
x er 1 til 6; x is 1 to 6;
eller med den generelle formel: or with the general formula:
hvor X er -0H eller -NH^ og R er en alkylgruppe med 1-5 carbonatomer, og/eller polyforfat, f.eks. natriumpolyfosfater eller fosfatestere, med formelen: where X is -OH or -NH^ and R is an alkyl group with 1-5 carbon atoms, and/or polyforfat, e.g. sodium polyphosphates or phosphate esters, with the formula:
hvor M er H, NH^ eller et énverdig metallion, og R er en alkylengruppe med 1-18 carbonatomer. Passende polyfosfater er angitt i US patenter 2.337.856, 2.906.599 og 3.213.017. De fore-trukne forbindelser er imidlertid amino-tris-(methylenfosfonsyre) og hydroxyethyliden-l,l-difosfonsyre (HEDP) og vannoppløselige salter derav. where M is H, NH^ or a monovalent metal ion, and R is an alkylene group with 1-18 carbon atoms. Suitable polyphosphates are disclosed in US Patents 2,337,856, 2,906,599 and 3,213,017. However, the preferred compounds are amino-tris-(methylenephosphonic acid) and hydroxyethylidene-1,1-diphosphonic acid (HEDP) and water-soluble salts thereof.
Passende høymolekylære polymerer omfatter en hvilken som helst ikke-ionisk eller anionisk yannoppløselig polymer med en molekylyekt på minst 100.000, og fortrinnsvis minst 1.000.000. Eksempler på passende polymerer omfatter polyacrylamider som dem som er angitt i U .S. patent 3-085.916, polymerer av 2-acrylamido-methyl-propan-sulfonsyre som dem som er angitt i U.S. patent 3.709.816, og sulfonerte polystyrener som dem som er angitt i U.S. patent 3-630.937. Suitable high molecular weight polymers include any nonionic or anionic water soluble polymer with a molecular weight of at least 100,000, and preferably at least 1,000,000. Examples of suitable polymers include polyacrylamides such as those disclosed in U .S. patent 3-085,916, polymers of 2-acrylamido-methyl-propane-sulfonic acid such as those disclosed in U.S. Pat. patent 3,709,816, and sulfonated polystyrenes such as those disclosed in U.S. Pat. patent 3-630,937.
Oppfinnelsen belyses ytterligere av følgende eksempler: The invention is further illustrated by the following examples:
Eksempel 1 Example 1
10 ppm av et preparat inneholdende en høymolekylær copolymer av 2-acrylamido-methyl-propan-sulfonsyre og acrylamid og en skallinhibitor [amino-tris-(methylenfosfonat)] i et vektforhold på 1:2,5 ble opprettholdt i vanntilførselen til gassvaskesystemet til en basisk oxygenovn i 13 uker på hvilket tidspunkt systemet ble inspisert visuelt og ingen synlig avsetning kunne iakttaes i pumpene, ventilene eller dusjene. Dette står i motsetning til 10 ppm of a preparation containing a high molecular weight copolymer of 2-acrylamido-methyl-propane-sulfonic acid and acrylamide and a shell inhibitor [amino-tris-(methylenephosphonate)] in a weight ratio of 1:2.5 was maintained in the water supply to the gas scrubbing system for a basic oxygen furnace for 13 weeks at which time the system was visually inspected and no visible deposits could be observed in the pumps, valves or showers. This is in contrast to
, sterk forurensning av pumper, dusjer og ventiler som førte til tap av gassvaske- og kjøleeffektivitet, og derpå bevirket midler- , heavy contamination of pumps, showers and valves which led to a loss of gas scrubbing and cooling efficiency, and subsequently caused means-
tidig produksjonstap, som forekom i en to-ukers periode uten behandling. Tidligere var dette system sterkt forurenset med calciumcarbonat og inneholdt betraktelige mengder ferrioxyd. early production loss, which occurred during a two-week period without treatment. Previously, this system was heavily contaminated with calcium carbonate and contained considerable amounts of ferric oxide.
Eksempel 2 Example 2
6,6 ppm av et preparat inneholdende en høymolekylær copolymer av 2-acrylamido-methyl-propan-sulfonsyre og acrylamid og en skallinhibitor [amino-tris-(methylenfosfonat)] i et vektforhold på 1:2,5 ble opprettholdt i vanntilførselen til kjølesystemet til en basisk oxygenovn og venturivaskesystemet som hadde en sterk oppbygning av calciumfluorid, jernoxyd og calciumcarbonat. Efter 1.600 oppvarmninger ble systemet inspisert, og gassled-ningene, avløpsrister og dyser viste seg å være rene. 6.6 ppm of a preparation containing a high molecular weight copolymer of 2-acrylamido-methyl-propane-sulfonic acid and acrylamide and a shell inhibitor [amino-tris-(methylenephosphonate)] in a weight ratio of 1:2.5 was maintained in the water supply to the cooling system to a basic oxygen furnace and the venturi washing system which had a strong build-up of calcium fluoride, iron oxide and calcium carbonate. After 1,600 heatings, the system was inspected, and the gas lines, drain grates and nozzles were found to be clean.
Eksempel 3 Example 3
15 ppm av et preparat inneholdende en høymolekylær copolymer av 2-acrylamido-methyl-propan-sulfonsyre og acrylamid og en skallinhibitor [amino-tris-(methylenfosfonat)] i et vektforhold på 1:2,5 ble opprettholdt i vanntilførselen til gassvaskesystemet til en masovn med store jernavsetninger, som tidligere hadde ført til et øket topptrykk i ovnen, hvilket førte til produksjonstap i ovnen og nedstengning for skallrensning innen en uke når ét lavmolekylaert (1.000) polyacrylat og amino-tris-(methylénfosf onat) ble anvendt. Efter 6 ukers behandling med de høymolekylær polymer-skallinhibitorpreparater ifølge oppfinnelsen, ble ingen trykkøkning eller oppbygning iakttatt, og systemet arbeidet, normalt. 15 ppm of a preparation containing a high molecular weight copolymer of 2-acrylamido-methyl-propane-sulfonic acid and acrylamide and a shell inhibitor [amino-tris-(methylenephosphonate)] in a weight ratio of 1:2.5 was maintained in the water supply to the gas scrubbing system for a blast furnace with large iron deposits, which had previously led to an increased top pressure in the furnace, which led to production loss in the furnace and shutdown for shell cleaning within a week when one low molecular weight (1,000) polyacrylate and amino-tris-(methylene phosphonate) was used. After 6 weeks of treatment with the high-molecular polymer shell inhibitor preparations according to the invention, no pressure increase or build-up was observed, and the system worked normally.
Eksempel 4 Example 4
For å simulere betingelser i et gassvaskesystem ble der fremstilt et syntetisk vann som hadde en pH på 12,0, en konsentrasjon av suspendert faststoff, (hydratisert ferrioxyd) på 2.000 mg/l, en konsentrasjon av natriumhydroxyd på 200 mg/l, en konsentrasjon av natriumbicarbonat på 26o mg/l, en calciumkonsentrasjon på In order to simulate conditions in a gas washing system, a synthetic water was produced which had a pH of 12.0, a concentration of suspended solids, (hydrated ferric oxide) of 2,000 mg/l, a concentration of sodium hydroxide of 200 mg/l, a concentration of of sodium bicarbonate of 26o mg/l, a calcium concentration of
450 mg/l og' en fluoridkonsentrasjon på 40 mg/l. Vannet ble holdt på en temperatur på 6ot2°C og sirkulert gjennom forsøkssystemet med en lineær hastighet mellom 90 og 120 cm/sek. Forsøkssystemet inneholdt en uoppvarmet forsøksdel (30 cm lang), en oppvarmet del (30 cm lang), en dusjedel og en avrenningsdel. Inhibitoren ble tilsatt til det syntetiske vann som så ble sirkulert gjennom systemet i 5 timer, hvorefter systemet ble nedstengt og forsøks- 450 mg/l and a fluoride concentration of 40 mg/l. The water was maintained at a temperature of 6ot2°C and circulated through the test system at a linear velocity between 90 and 120 cm/sec. The test system contained an unheated test part (30 cm long), a heated part (30 cm long), a shower part and a drainage part. The inhibitor was added to the synthetic water which was then circulated through the system for 5 hours, after which the system was shut down and experimental
delene veiet og den prosentvise inhibering ble beregnet i henhold til følgende formel: the parts weighed and the percentage inhibition were calculated according to the following formula:
Resultatene av disse forsøk er angitt i tabell I. The results of these experiments are set out in Table I.
Produktbetegnelser Product designations
"Calgon" natriumhexametafosfat "Calgon" sodium hexametaphosphate
AMP amino-t ris-(methylen-fosfonsyre) AMP amino-tris-(methylene-phosphonic acid)
HEDP 1-hydroxyethyliden-1,1-difosfonsyre HEDP 1-hydroxyethylidene-1,1-diphosphonic acid
Polymer 1 49/51 copolymer av acrylamid og 2-acrylamido-2-methyl-propan-l-sulfonsyre med en molekylvekt på ca. 1.000.000 Polymer 1 49/51 copolymer of acrylamide and 2-acrylamido-2-methyl-propane-1-sulfonic acid with a molecular weight of approx. 1,000,000
Polymer 2 homopolymer av 2-acrylamido-2-methyl-propan-l-sulfonsyre med en molekylvekt på ca. 500.000 Polymer 3 høymolekylær uhydrolysert polyacrylamid med en Polymer 2 homopolymer of 2-acrylamido-2-methyl-propane-1-sulfonic acid with a molecular weight of approx. 500,000 Polymer 3 high molecular unhydrolyzed polyacrylamide with a
molekylvekt på ca. 1.0OO.000 molecular weight of approx. 1,000,000
Polymer 4 høymolekylærc fhydrolysert (15%) polyacrylamid med en molekyl velet på ca. 1.000.000 Polymer 4 high molecular hydrolyzed (15%) polyacrylamide with a molecular weight of approx. 1,000,000
Polymer 5 sulfonert polystyren med en molekylvekt på ca. Polymer 5 sulphonated polystyrene with a molecular weight of approx.
700.000 700,000
Claims (2)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US64725376A | 1976-01-07 | 1976-01-07 | |
US73372376A | 1976-10-26 | 1976-10-26 |
Publications (3)
Publication Number | Publication Date |
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NO764352L NO764352L (en) | 1977-07-08 |
NO144619B true NO144619B (en) | 1981-06-29 |
NO144619C NO144619C (en) | 1981-10-07 |
Family
ID=27095118
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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NO764352A NO144619C (en) | 1976-01-07 | 1976-12-23 | PROCEDURE AND PREPARATION FOR AA FIGHT AGAINST DISPOSAL BUILDING IN GAS WASHERS |
Country Status (15)
Country | Link |
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JP (1) | JPS52110288A (en) |
BR (1) | BR7608838A (en) |
CA (1) | CA1087480A (en) |
CH (1) | CH624368A5 (en) |
DE (1) | DE2700347A1 (en) |
DK (1) | DK153367C (en) |
FI (1) | FI763638A (en) |
FR (1) | FR2337694A1 (en) |
GB (1) | GB1532391A (en) |
IE (1) | IE44558B1 (en) |
IT (1) | IT1121700B (en) |
LU (1) | LU76525A1 (en) |
NL (1) | NL185221C (en) |
NO (1) | NO144619C (en) |
SE (1) | SE435456B (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
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GB2019826B (en) * | 1978-04-28 | 1982-06-23 | Martin Marietta Corp | Process of removing oxides of sulphur from gases sludge resulting from process and product comprising lime or limestone |
CA1114978A (en) * | 1978-06-15 | 1981-12-22 | Chih M. Hwa | Sludge conditioning composition for scale inhibition in water |
JPS55109432A (en) * | 1979-02-19 | 1980-08-22 | Kurita Water Ind Ltd | Deodorizing method |
US4342733A (en) * | 1981-01-09 | 1982-08-03 | Betz Laboratories, Inc. | Method of improving sulfite antioxidant performance in high solids scrubbers |
DE3230291A1 (en) * | 1981-08-18 | 1983-03-03 | Dearborn Chemicals Ltd., Widnes, Cheshire | COMPOSITION FOR PREVENTING KETTLE IN AQUEOUS SYSTEMS |
US4588519A (en) * | 1982-01-29 | 1986-05-13 | Dearborn Chemical Company | Method of inhibiting corrosion of iron base metals |
CA1207211A (en) * | 1982-09-27 | 1986-07-08 | Dionisio G. Cuisia | Composition and method for inhibiting scale |
US4469663A (en) * | 1982-10-15 | 1984-09-04 | The Dow Chemical Company | Scale control in flue gas desulfurization |
CA1258963A (en) * | 1983-03-07 | 1989-09-05 | Bennett P. Boffardi | Synergistic scale and corrosion inhibiting admixtures containing carboxylic acid/sulfonic acid polymers |
DE3317126C2 (en) * | 1983-05-06 | 1986-07-24 | Mannesmann AG, 4000 Düsseldorf | Process to avoid acid corrosion on continuous casting plants |
US4671934A (en) * | 1986-04-18 | 1987-06-09 | Buckman Laboratories, Inc. | Aminophosphonic acid/phosphate mixtures for controlling corrosion of metal and inhibiting calcium phosphate precipitation |
US4872996A (en) * | 1987-03-13 | 1989-10-10 | The Dow Chemical Company | Use of aminophosphonic acids to inhibit scale formation and corrosion caused by manganese in water systems |
EP0311072A3 (en) * | 1987-10-08 | 1989-06-07 | The B.F. Goodrich Company | Stabilization of metal ions and dispersion of particulates in aqueous systems |
CN108136367A (en) * | 2015-08-28 | 2018-06-08 | 塞里奥尼克斯股份有限公司 | For the pneumatic filter of alkaline pollutant |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
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GB1110365A (en) * | 1965-03-29 | 1968-04-18 | Calgon Corp | Inhibition of scale in saline water evaporators |
FR1544503A (en) * | 1966-11-16 | 1968-10-31 | Benckiser Gmbh Joh A | Descaler products |
US3630937A (en) * | 1968-05-06 | 1971-12-28 | Calgon Corp | Sulfonated polystyrene compositions and methods of treating boiler water |
CA952784A (en) * | 1970-08-28 | 1974-08-13 | Chemed Corporation | Scale-inhibiting composition and method |
US3663448A (en) * | 1970-09-25 | 1972-05-16 | Calgon Corp | Inhibiting scale deposition |
US3709816A (en) * | 1971-07-01 | 1973-01-09 | Calgon Corp | Control of alluvial and other deposits in aqueous systems |
US3806367A (en) * | 1972-06-01 | 1974-04-23 | Bitz Lab Inc | Acrylamido-sulfonic acid polymers and their use as rust and tubercle removing agents |
FR2198106A1 (en) * | 1972-09-04 | 1974-03-29 | Rhone Progil | Corrosion and scale prevention in cooling systems - using phosphates, zinc salts and acrylic polymers |
DE2248586A1 (en) * | 1972-10-04 | 1974-04-18 | Drew Chem Corp | METHOD OF SEPARATION OF ACID GASES FROM MIXTURES OF FLUIDS CONTAINING SUCH GASES |
US3890228A (en) * | 1973-04-13 | 1975-06-17 | Chemed Corp | Polyacrylate-polyphosphonic acid treatment in aqueous systems |
US3918935A (en) * | 1973-08-13 | 1975-11-11 | Factory Mutual Res Corp | Non-newtonian liquid and method for wet scrubbing stack gases |
US3880620A (en) * | 1974-06-19 | 1975-04-29 | Betz Laboratories | Method for scrubbing gases derived from blast furnaces |
-
1976
- 1976-12-15 SE SE7614102A patent/SE435456B/en not_active IP Right Cessation
- 1976-12-16 DK DK566776A patent/DK153367C/en not_active IP Right Cessation
- 1976-12-17 FI FI763638A patent/FI763638A/fi not_active Application Discontinuation
- 1976-12-21 NL NLAANVRAGE7614213,A patent/NL185221C/en not_active IP Right Cessation
- 1976-12-23 NO NO764352A patent/NO144619C/en unknown
- 1976-12-30 BR BR7608838A patent/BR7608838A/en unknown
- 1976-12-31 IT IT52856/76A patent/IT1121700B/en active
- 1976-12-31 IE IE2858/76A patent/IE44558B1/en not_active IP Right Cessation
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1977
- 1977-01-04 GB GB46/77A patent/GB1532391A/en not_active Expired
- 1977-01-04 CA CA269,079A patent/CA1087480A/en not_active Expired
- 1977-01-05 DE DE19772700347 patent/DE2700347A1/en active Granted
- 1977-01-05 FR FR7700135A patent/FR2337694A1/en active Granted
- 1977-01-05 LU LU76525A patent/LU76525A1/xx unknown
- 1977-01-06 CH CH15477A patent/CH624368A5/en not_active IP Right Cessation
- 1977-01-07 JP JP43977A patent/JPS52110288A/en active Pending
Also Published As
Publication number | Publication date |
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DK153367B (en) | 1988-07-11 |
NL185221B (en) | 1989-09-18 |
DE2700347C2 (en) | 1989-12-28 |
CA1087480A (en) | 1980-10-14 |
FR2337694A1 (en) | 1977-08-05 |
DK566776A (en) | 1977-07-08 |
IE44558B1 (en) | 1982-01-13 |
SE435456B (en) | 1984-10-01 |
NL185221C (en) | 1990-02-16 |
IT1121700B (en) | 1986-04-10 |
DE2700347A1 (en) | 1977-07-14 |
DK153367C (en) | 1989-01-02 |
CH624368A5 (en) | 1981-07-31 |
IE44558L (en) | 1977-07-07 |
NL7614213A (en) | 1977-07-11 |
FR2337694B1 (en) | 1981-12-24 |
NO764352L (en) | 1977-07-08 |
LU76525A1 (en) | 1977-07-15 |
BR7608838A (en) | 1977-10-25 |
JPS52110288A (en) | 1977-09-16 |
SE7614102L (en) | 1977-07-08 |
FI763638A (en) | 1977-07-08 |
GB1532391A (en) | 1978-11-15 |
NO144619C (en) | 1981-10-07 |
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