RU2003107342A - METHOD FOR PRODUCING IRON OXIDES - Google Patents

METHOD FOR PRODUCING IRON OXIDES

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Publication number
RU2003107342A
RU2003107342A RU2003107342/15A RU2003107342A RU2003107342A RU 2003107342 A RU2003107342 A RU 2003107342A RU 2003107342/15 A RU2003107342/15 A RU 2003107342/15A RU 2003107342 A RU2003107342 A RU 2003107342A RU 2003107342 A RU2003107342 A RU 2003107342A
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RU
Russia
Prior art keywords
iron
oxides
oxygen
carboxylate
carboxylic acid
Prior art date
Application number
RU2003107342/15A
Other languages
Russian (ru)
Other versions
RU2318730C2 (en
Inventor
Эстерино Конка
Карло Рубини
Гвидо Петрини
Original Assignee
Зюд Кеми Мт С.Р.Л.
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.)
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Publication date
Priority claimed from IT2002MI000567A external-priority patent/ITMI20020567A1/en
Application filed by Зюд Кеми Мт С.Р.Л. filed Critical Зюд Кеми Мт С.Р.Л.
Publication of RU2003107342A publication Critical patent/RU2003107342A/en
Application granted granted Critical
Publication of RU2318730C2 publication Critical patent/RU2318730C2/en

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Claims (9)

1. Способ получения оксидов железа высокой чистоты, содержащий следующие стадии, осуществляемые последовательно или одновременно: а) взаимодействие металлического железа в виде микрошаровидных частиц, имеющих средний диаметр не более 250 мкм, либо в виде скрапа или обрезков, размеры которых таковы, что их площадь на кг железа и на литр реакционной среды составляет более 0,01 м2, с перемешиваемым водным раствором карбоновой кислоты, содержащей одну или несколько карбоновых групп с рКа от 0,5 до 6 при температуре окружающей среды относительно первого карбоксила, способной разлагаться при нагревании в воздухе при температуре от 200 до 350° С на двуокись углерода и воду, а также образовывать соли железа (II), растворимые в водном растворе при условиях взаимодействия, при этом соотношение между молями карбоновой кислоты и г-атомами железа составляет от 0,03 до 1,5, массовое соотношение вода/железо составляет от 1 до 20, температура взаимодействия составляет от 0 до 100° С, и микрошаровидные частицы удерживают в суспензии перемешиванием; b) окисление до карбоксилата железа (III) карбоксилата железа (II), получаемого на стадии а), окислителем, выбранным из кислорода, кислород-содержащей газообразной смеси, перекиси водорода, озона, органических перекисей и гидроперекисей, и применяемым в избытке относительно стехиометрического количества соли железа (II), окисляемой в соль железа (III).1. A method of producing high purity iron oxides, comprising the following stages, carried out sequentially or simultaneously: a) the interaction of metallic iron in the form of microspherical particles having an average diameter of not more than 250 microns, or in the form of scrap or scraps, the sizes of which are such that their area per kg of iron and per liter of the reaction medium is more than 0.01 m 2 , with a stirred aqueous solution of a carboxylic acid containing one or more carboxylic groups with pKa from 0.5 to 6 at ambient temperature relative to vodka carboxyl, capable of decomposing upon heating in air at temperatures from 200 to 350 ° C into carbon dioxide and water, and also to form iron (II) salts, soluble in an aqueous solution under the conditions of interaction, while the ratio between moles of carboxylic acid and g- iron atoms is from 0.03 to 1.5, the mass ratio of water / iron is from 1 to 20, the interaction temperature is from 0 to 100 ° C, and the microspherical particles are kept in suspension by stirring; b) oxidation to iron (III) carboxylate of iron (II) carboxylate obtained in stage a), an oxidizing agent selected from oxygen, an oxygen-containing gaseous mixture, hydrogen peroxide, ozone, organic peroxides and hydroperoxides, and used in excess relative to the stoichiometric amount salts of iron (II), oxidized to a salt of iron (III). 2. Способ по п.1, в котором температура взаимодействия составляет от 5 до 70° С, а молярное соотношение между карбоновой кислотой и г-атомами железа составляет от 0,05 до 0,8.2. The method according to claim 1, in which the interaction temperature is from 5 to 70 ° C, and the molar ratio between carboxylic acid and g-iron atoms is from 0.05 to 0.8. 3. Способ по п.1 или 2, в котором кислород или перекись водорода применяют в качестве окислителя.3. The method according to claim 1 or 2, in which oxygen or hydrogen peroxide is used as an oxidizing agent. 4. Способ по любому из предыдущих пп.1, 2 или 3, в котором частицы микрошаровидного железа имеют средний диаметр менее 200 мкм.4. The method according to any of the preceding claims 1, 2 or 3, in which the particles of microspheroidal iron have an average diameter of less than 200 microns. 5. Способ по любому из пп.1-4, в котором содержание углерода в железе составляет менее 0,15 мас.%, а содержание легирующих элементов составляет менее 0,3 мас.%5. The method according to any one of claims 1 to 4, in which the carbon content in iron is less than 0.15 wt.%, And the content of alloying elements is less than 0.3 wt.% 6. Способ получения оксидов железа высокой чистоты, содержащий окисление окислителем, выбранным из кислорода, кислород-содержащих газообразных смесей, перекиси водорода, озона, органических перекисей и гидроперекисей, применяемых в избытке относительно стехиометрического количества железа, окисляемого из иона железа (II) в ион железа (III), заранее полученного карбоксилата железа (II) карбоновой кислоты, рКа первого карбоксила которой составляет от 0,5 до 6 и которая способна разлагаться при нагревании от 200 до 350° С на СО2 и Н2О, либо смесей указанного карбоксилата с карбоновой кислотой, описанной выше, причем водный раствор карбоксилата подвергают взаимодействию с железом в виде микрошаровидных частиц со средним диаметром менее 250 мкм, либо с железной токарной стружкой или скрапом, имеющими такие размеры, что площадь их поверхности на кг железа и на литр раствора составляет более 0,01 м2, и при этом молярное соотношение аниона, присутствующего в соли и кислоте, и г-атомов железа составляет от 0,03 до 1,5, массовое соотношение вода/железо составляет от 1 до 20, температура взаимодействия составляет от 0 до 100° С, а микрошаровидное железо удерживают в суспензии перемешиванием.6. A method of producing high purity iron oxides, comprising oxidizing with an oxidizing agent selected from oxygen, oxygen-containing gaseous mixtures, hydrogen peroxide, ozone, organic peroxides and hydroperoxides, used in excess relative to the stoichiometric amount of iron oxidized from an iron (II) ion to an ion iron (III), a pre-prepared carboxylate of iron (II) carboxylic acid, the pKa of the first carboxyl of which is from 0.5 to 6 and which can decompose upon heating from 200 to 350 ° C into CO 2 and H 2 O, or mixtures indicated a carboxylate with a carboxylic acid as described above, wherein the aqueous carboxylate solution is reacted with iron in the form of microspherical particles with an average diameter of less than 250 microns, or with iron turning chips or scraps having such dimensions that their surface area per kg of iron and per liter the solution is more than 0.01 m 2 , and the molar ratio of the anion present in salt and acid to g-iron atoms is from 0.03 to 1.5, the mass ratio of water / iron is from 1 to 20, the interaction temperature I ranges from 0 to 100 ° C, and the microspherical iron is kept in suspension by stirring. 7. Оксиды FeOOH, имеющие удельную площадь поверхности от 1 до 300 м2/г; магемит (Fe2O3), имеющий удельную площадь поверхности 1-15 м2/г, при этом указанные оксиды свободны от щелочных и/или щелочноземельных ионов и/или ионов аммония, а также анионов сульфата и/или хлорида.7. FeOOH oxides having a specific surface area of from 1 to 300 m 2 / g; magemite (Fe 2 O 3 ) having a specific surface area of 1-15 m 2 / g, while these oxides are free from alkaline and / or alkaline earth ions and / or ammonium ions, as well as sulfate and / or chloride anions. 8. Пигменты, полученные из оксидов железа по п.7.8. Pigments obtained from iron oxides according to claim 7. 9. Катализаторы, содержащие оксиды железа по п.7 или полученные из оксидов по п.7.9. Catalysts containing iron oxides according to claim 7 or obtained from oxides according to claim 7.
RU2003107342/15A 2002-03-18 2003-03-17 Method of production of the ferric oxides RU2318730C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ITMI2002A000567 2002-03-18
IT2002MI000567A ITMI20020567A1 (en) 2002-03-18 2002-03-18 PROCESS FOR THE PREPARATION OF IRON OXIDES

Publications (2)

Publication Number Publication Date
RU2003107342A true RU2003107342A (en) 2004-09-10
RU2318730C2 RU2318730C2 (en) 2008-03-10

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US (4) US6790274B2 (en)
EP (1) EP1350765B1 (en)
JP (2) JP4658456B2 (en)
CN (1) CN100475708C (en)
AR (1) AR038989A1 (en)
AT (1) ATE337270T1 (en)
CA (1) CA2421363C (en)
DE (1) DE60307710T2 (en)
DK (1) DK1350765T3 (en)
IT (1) ITMI20020567A1 (en)
MX (1) MXPA03002330A (en)
RU (1) RU2318730C2 (en)
ZA (1) ZA200301584B (en)

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