PL104851B1 - METHOD OF REMOVING HYDROGEN FROM GASES - Google Patents
METHOD OF REMOVING HYDROGEN FROM GASES Download PDFInfo
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- PL104851B1 PL104851B1 PL19631977A PL19631977A PL104851B1 PL 104851 B1 PL104851 B1 PL 104851B1 PL 19631977 A PL19631977 A PL 19631977A PL 19631977 A PL19631977 A PL 19631977A PL 104851 B1 PL104851 B1 PL 104851B1
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Przedmiotem wynalazku jest sposób usuwania fluorowodoru z gazów odlotowych, powstajacych w procesach wytwarzania nawozów sztucznych, fosforanów paszowych, aluminium czy emalii.The invention relates to a removal method hydrogen fluoride from the resulting waste gases in the production of artificial fertilizers, feed phosphates, aluminum or enamel.
Dokladne usuwanie zwiazków fluoru z gazów odlotowych jest konieczne, poniewaz stanowia one powazne zagrozenie dla srodowiska.Thorough removal of fluorine compounds from gases departure is necessary because they provide serious threat to the environment.
Dotychczas znane sposoby usuwania fluorowo¬ doru z gazów odlotowych polegaja na aibsiorpcjii tego skladnika w wodzie lob w wodnych roztwo¬ rach lub zawiesinach substancji alkalicznych, przy czym jako substancja alkaliczna moze byc zasto¬ sowany wodorotlenek metalu alkalicznego, weglan meitalu alkalicznego lub wodorotlenek wapniowy.Hitherto known methods of removal of fluorine of exhaust gas rely on aibsorption of this ingredient in water or in an aqueous solution alkaline substances or suspensions, e.g. what it can be used as an alkaline substance alkali metal hydroxide, carbonate alkaline meital or calcium hydroxide.
Metalem alkalicznymi jest zwykle sód. Absorpcja przebiega w srodowisku kwasnym gdy czynni¬ kiem wymywajacym jest woda, lub w srodowi¬ sku aflkalicznyim gidy czynnikiem wymywajacym sa wymienione zwiajzki metali alkalicznych lub wapnia w postaci wodnego roztworu iuib wodnej zawiesiny.The alkali metal is usually sodium. Absorption takes place in an acidic environment when active the leaching fluid is water, or in the environment the effect of aflkalic gidy leaching agent alkali metal compounds or calcium in the form of an aqueous solution of aqueous iuib suspensions.
Przerób roztworów poabsorpcyjnych dlai powyz¬ szych metod jest utrudniony z powodu malych stezen zwaazków fluoru w tych roztworach^ co wynika z niewielkiej rozpuszczalnosci fluorku so¬ dowego i wapniowego w wodzie.Working up of the absorbent solutions for and above the lower methods are difficult because of the small ones the concentration of fluorine compounds in these solutions is due to the low solubility of sodium fluoride and calcium in water.
W przypadku oczyszczania gazów odlotowych, posiadajacych zwykle niskie stezenie fluorowodoru rzedu ponizej 6 g/Nm3 i podwyzszona tempe¬ rature rzedu 200°C metoda mycia wodnego nie jest mozliwe otrzymanie stezonych roztworów kwasu fluorowodorowego z powodu wysokiej prez¬ nosci pojTCJalnej fluorowodoru w teiruperaAurach roztworu 50 do 70°C.In the case of waste gas treatment, usually with a low concentration of hydrogen fluoride of less than 6 g / Nm3 and elevated temperature rature at 200 ° C water washing method no it is possible to obtain concentrated solutions hydrofluoric acid due to high pres Carrying of Capable Hydrogen Fluoride in TeiruperAurach 50 to 70 ° C solution.
Sposób usuwania fluorowodoru z gazów prze¬ myslowych wedlug wynalazku polega na dwusto¬ pniowej absorpcji za pomoca wodnych roztwo¬ rów fluorku amonowego i wodorofluoTku amo- nowiego.The method of removing hydrogen fluoride from exhaust gases according to the invention is two hundred truncated absorption with aqueous solutions ammonium fluoride and ammonium hydrofluoride new one.
W pierwszym stopniu absoTpcji laczne stezenie fluorku i wodorofluorku amonowego wynosi 1 do 40% wagowych, a stosunek molowy fluorowodoru do fluorku amonowego w roztworze wymywaja- cym wynosi od 0,2 do 2,5.Total concentration in the first degree of absorption of fluoride and ammonium hydrofluoride is 1 to 40% by weight, molar ratio of hydrogen fluoride to ammonium fluoride in solution eluting cym ranges from 0.2 to 2.5.
Natomiast w drugim stopniu * absorpcji laczne stezenie fluOirku i wodorofluorku omanowego wy¬ nosi 1 do 25°/o wagowych, a stosunek molowy fluorowodoru do fluorku amonowego w roztwo¬ rze wymywajacym wynosi od 0,05 do lfi. Roztwór wymywajacy z drugiego stopnia absorpcji wpro¬ wadzany jest do roztworu wymywajacego w pierwszym stopniu absorpcji, niatomliast roztwór z pierwszego stopnia absorpcji wiprowadzany jest na zewnatrz ukladu aibsorpcyjnego. Odipowiedni stosunek molowy fluorowodoru do fluorku amono¬ wego w roztworach wymywajacych utrzymuje sie przez wprowadzenie wody amoniakalnej lub ga¬ zowego amOniiaku.However, in the second stage * total absorption the concentration of fluoro and oman hydrofluoride it is 1 to 25% by weight and the molar ratio hydrogen fluoride to ammonium fluoride in solution the leaching temperature ranges from 0.05 to lfi. Solution leaching from the second degree of absorption into it is poured into a solution washing v first stage of absorption, niatomliast solution from the first absorption stage is carried out outside the absorption system. Appropriate the molar ratio of hydrogen fluoride to ammonium fluoride persistence in the washing solutions by introducing ammonia water or gas new amOniiak.
Fluorek amonowy i wodorofliuorek amonowy sa dobrze rozpuszczalne w wod&ie, co umozliwia pnro- 104851104851 wadzenie absorpcji za pomoca roztworów o du¬ zym stezeniu fludru. Absorpcja fluorowodoru na¬ stepuje nawet przy silnym przekwaszeniu roz- tiwoirui, poniewaz tworza sie zwiazki typu (NH4F)n«((HiF)m, przy czym iloraz m:n moze wy¬ nosic 2 lub wiecej. Jest to zjawisko- korzystne, poniewaz w ten sposób mozna uzyskiwac roz¬ twory poabsorpcyjine o duzej zawartosci fluoru, naitoimiast ilosc jonu amonowego wprowadzanego do ukladu absorpcyjnego moze byc niewielka.Ammonium fluoride and ammonium hydrofluoride are well soluble in water, which enables 104851104851 absorption with large solutions a bad concentration of fludru. Absorption of hydrogen fluoride by na¬ tapping even with strong acidification tiwoirui, because it forms compounds of the type (NH4F) n "((HiF) m, with the quotient m: n being possible wear 2 or more. It is a phenomenon that because in this way a solution can be obtained postabsorption formations with a high content of fluoride, the amount of ammonium ion introduced to the absorption system can be small.
Otrzymany roztwór poabsorpcyjhy moze byc prze¬ rabiany nai wodorofJjuoirek amonowy w postaci krystalicznej lub stopu albo na fluorek sodowy.The obtained absorption solution can be transformed into rabiany nai hydrogenofJjuoirek ammonium in the form crystalline or alloy or sodium fluoride.
Przyklad. Gaz pobieramy z odpylini pieca do produkcji termofosifatu paszowego wpTOwadzo.no w ciagu godziny do pierwszego stopnia absorpcji dwustopniowego uradzenia absorpcyjnego insta¬ lacji modelowej w ilosci 500 Nm3 który zawieral 1,06 kg HF. Jako roztwór absorpcyjny wprowa¬ dzono 3il,9l23 kg wody, 0,3^2 kg amoniaku i 8,774 kg roztworu z drugiego stopnia absorpcji o skladzie: 0,0% NH4HF2 i 0,6% NH4tF. W wyniku absorpcji przeprowadzonej w temperaturze 76QC, otrzyma- no 690,30 kg gazu zawierajacego 0,105 kg HF oraz 7,006 kg roztwoiru zawierajacego 17/7% NH4HF2 i 2,3% HF. Gaz skierowano do drugiego* stopnia absorpcji urzadzenlia absorpcyjnego, do którego Wprowadzano równiez 8,642 kg wody i 0,0477 kg amoniaku.Example. We take gas from the dust collector of the furnace to production of feed thermophosphate wpTOwadzo.no within an hour to the first degree of absorption of a two-stage absorption plant modeling in the amount of 500 Nm3 it contained 1.06 kg HF. Introduce as the absorption solution 3L, 9L23 kg of water, 0.3-2 kg of ammonia and 8.774 kg were added a solution from the second absorption stage composed of: 0.0% NH4HF2 and 0.6% NH4tF. As a result of absorption carried out at the temperature of 76 ° C, obtained no 690.30 kg of gas containing 0.105 kg of HF and 7.006 kg of a solution containing 17/7% NH4HF2 and 2.3% HF. The gas was diverted to the second * stage absorption absorption device to which Also 8.642 kg of water and 0.0477 kg were introduced ammonia.
Afasoirpcje przeprowadzono w temperaturze 57°C.The treatments were carried out at 57 ° C.
Otrzymany roztwór poaibsorpcyjny w ilosci 8,774 kg i o skladzie 0,0% NH4HF2 i 0,6% NH4F skierowa¬ no do pierwszego stopnia absorpcji. Urzadzenie absorpcyjne opuszcza gaz w ilosci 669,30 kg za¬ wierajacy 0,021 kg HF. Stopien Wymycia fluoro¬ wodoru wynosi* 98%.The obtained absorbent solution in the amount of 8.774 kg and containing 0.0% NH4HF2 and 0.6% NH4F as directed up to the first degree of absorption. Equipment absorptive gas leaves the gas in an amount of 669.30 kg per 0.021 kg HF. Fluoride Washout Rate hydrogen is * 98%.
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PL19631977A PL104851B1 (en) | 1977-02-26 | 1977-02-26 | METHOD OF REMOVING HYDROGEN FROM GASES |
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PL19631977A PL104851B1 (en) | 1977-02-26 | 1977-02-26 | METHOD OF REMOVING HYDROGEN FROM GASES |
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PL196319A1 PL196319A1 (en) | 1978-08-28 |
PL104851B1 true PL104851B1 (en) | 1979-09-29 |
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US8618436B2 (en) | 2006-07-14 | 2013-12-31 | Ceramatec, Inc. | Apparatus and method of oxidation utilizing a gliding electric arc |
US8350190B2 (en) | 2007-02-23 | 2013-01-08 | Ceramatec, Inc. | Ceramic electrode for gliding electric arc |
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