SU203637A1 - METHOD OF PREPARATION OF CHEMICAL CATALYST - Google Patents
METHOD OF PREPARATION OF CHEMICAL CATALYSTInfo
- Publication number
- SU203637A1 SU203637A1 SU1009380A SU1009380A SU203637A1 SU 203637 A1 SU203637 A1 SU 203637A1 SU 1009380 A SU1009380 A SU 1009380A SU 1009380 A SU1009380 A SU 1009380A SU 203637 A1 SU203637 A1 SU 203637A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- catalyst
- preparation
- copper
- chemical catalyst
- chromic anhydride
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 title description 16
- 239000000126 substance Substances 0.000 title 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 13
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical class [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate dianion Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- 239000005751 Copper oxide Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- QPLDLSVMHZLSFG-UHFFFAOYSA-N copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 2
- 229910000431 copper oxide Inorganic materials 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N carbon dioxide Chemical class O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- -1 copper-chromium Chemical compound 0.000 description 1
- 230000000875 corresponding Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical class [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Chemical class 0.000 description 1
- 239000011701 zinc Chemical class 0.000 description 1
Description
Известен способ приготовлени катализатора дл конверсии ОКиси углерода путем смешени углекислых солей меди и цинка с хроМовым антидридо,м с последующим ynaipHisaнием , сушкой и таблетиро вамием катализаторной массы.A known method of preparing a catalyst for the conversion of oxyal carbon by mixing carbonic salts of copper and zinc with chromium antidrido, m followed by ynaipHis, drying and tabletting the catalyst mass.
С целью получени катализатора, активного в интервале температур 150-175°С с остаточным проденто.м окиси углерода в конвертированном газе 0,1-0,3%, -предлагаетс го.товить двухкОМпонентный катализатор с применением в качестве основного исходного сырь углекислой соли меди или гидрата окиси меди и хромового ангидрида в таком соотношении , чтО|бы содержание СгаОз в пересчете на roTOiBbm катализатор составл ло от 8 до 20 вес. %.In order to obtain a catalyst that is active in the temperature range of 150-175 ° C with a residual carbon monoxide in the converted gas of 0.1-0.3%, it is proposed to put a two-component catalyst using the carbon dioxide salt as the main feedstock. or hydrate of copper oxide and chromic anhydride in such a ratio that its content would be 8 to 20 weight, in terms of the roTOiBbm catalyst. %
При м е р. 1 вес. ч. хромового ангидрида СгОз раствОр ют в 3 вес. ч. дистиллированной воды. В отдельном сосуде готов т суспензию основной углекислой соли меди СиСОз Cui(OiH)2 в дистиллированной воде в соотношении 1 : 1. В суспензию основной углекислой соли меди при тщательном перемешивании постепенно добавл ют раствО)р хромового ангидрида в количестве, соответствую.щем 15% СгаОз в готовом катализаторе. Катализаторную массу интенсивно .перемешивают 2-3 час, затем, не прекраща перемешивани , упаривают до в зкой консистенции. После этого в зкую катализаторную Aiaccy выливают на противни и сушат на воздухе при 120-130° не менее 4 час. Катализатор измельчают и таблетируют на та блето.чной машине с да1влением прессовани не менее 1600 кгс/см2.An example. 1 weight. CrO3 chromic anhydride dissolved in 3 wt. including distilled water. In a separate vessel, a suspension of basic carbonate of copper CuSO (OiH) 2 in distilled water in a ratio of 1: 1 is prepared. To the suspension of basic carbonate of copper, with vigorous stirring, solution of chromic anhydride is gradually added in an amount corresponding to 15% Sgoaz in the finished catalyst. The catalyst mass is intensively stirred for 2-3 hours, then, without stopping the stirring, evaporated to a viscous consistency. After that, the viscous catalyst Aiaccy is poured onto trays and dried in air at 120-130 ° for at least 4 hours. The catalyst is crushed and pelletized on that machine with a pressing of at least 1600 kgf / cm2.
Удельна поверхность катализатора равна 20-45 , насыпной вес катализатора 1,16 кг/мз. Механическа прочность Hai раздавливание 90-98 кгс/см.The specific surface of the catalyst is 20–45, the bulk density of the catalyst is 1.16 kg / m3. Mechanical strength Hai crush 90-98 kgf / cm.
П р е д ,м е т изобретени PRED, METTES OF THE INVENTION
Способ приготовлени меднохромового катализатора дл конверсии о-киси углерода с вод ным паром путем смешени углекислой соли .меди или гидрата окиси меди и хромового ангидрида с добавлением воды, упариванием , сушкой и та:блетирование:М катализаторной массы, отличающийс тем, что-, с делью получени катализатора активного в интервале температур 150-175°С, хромовый ангидрид берут в количестве, обеспечивающем содержание окиси хрома в катализаторе от 8 до 20 вес. %.A method of preparing a copper-chromium catalyst for the conversion of o-carbonic acid with water vapor by mixing carbonate of copper or copper oxide and chromic anhydride with the addition of water, evaporation, drying and that: bleating: M catalyst mass, characterized in that, with In order to obtain a catalyst active in the temperature range of 150-175 ° C, chromic anhydride is taken in an amount that provides the content of chromium oxide in the catalyst from 8 to 20 weight. %
Publications (1)
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SU203637A1 true SU203637A1 (en) |
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