CN1045359A - The preparation method of iron-chromium-molybdenum system-carbonoxide transformation catalyst - Google Patents
The preparation method of iron-chromium-molybdenum system-carbonoxide transformation catalyst Download PDFInfo
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- CN1045359A CN1045359A CN 90101486 CN90101486A CN1045359A CN 1045359 A CN1045359 A CN 1045359A CN 90101486 CN90101486 CN 90101486 CN 90101486 A CN90101486 A CN 90101486A CN 1045359 A CN1045359 A CN 1045359A
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- chromium
- iron
- precipitation
- molybdate
- molybdenum
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Abstract
The present invention relates to the preparation method of a kind of iron chromium mo-series-carbonoxide transformation catalyst, it is that inorganic salts with the iron of solubility, chromium, molybdenum carry out co-precipitation in alkaline solution (NaOH, KOH), washs roasting then and beats sheet and form.This legal system gets catalyst has higher reactivity, better anti-efflorescence ability than the catalyst of traditional solid-state mixed grind method or mixed precipitation method preparation.
Description
The present invention relates to the preparation method of iron chromium mo-series-carbonoxide transformation catalyst, it is that domestic iron chromium mo-series method for preparing catalyst is improved.
The Fe-Cr-Mo that present medium and small synthesis ammonia plant adopted is that medium temperature shift catalyst (being the B112 type) is active good, sulfur tolerance is used widely by force, but this catalyst adopts the preparation of Fe-Cr-Mo solid mixed grind method, and easy efflorescence during use causes bed resistance big, can't continue to use, influence its service life, and the dust after its efflorescence is washed into down workshop section, causes the heat exchanger erosion corrosion, bring to the low stove that becomes and make low change catalyzer bias current and even active decline, make troubles to whole production.
It is a lot of both at home and abroad to prepare the report of siderochrome medium temperature shift catalyst for the siderochrome coprecipitation method in recent years, does not appear in the newspapers and prepare transformation catalyst for the coprecipitation of iron, chromium, molybdenum.Iron, chromium co-precipitation are that molysite with solubility is (as FeSO substantially
4, Fe(NO
3)
2Deng) and chromic anhydride in the aqueous solution, add the hydroxide that alkali generates Fe, Cr after miscible, add that then proper additive beats sheet and form (as Chinese B107, B108, B109, B113, B114; N721, " word portion " wave day in Japan; Britain ICI15-5; West Germany BASFK6-10; U.S. G-3A, G-3B, 9-38), and molybdenum be with molybdenum concntrate form (＞300 order) mixed grind in the oxide that Fe, Cr co-precipitation are generated (as Chinese B112).The catalyst iron content is with Fe
2O
3Count 60-90%, chromium content is with Cr
2O
3Count 5-10%, molybdenum content is with Mo
2O
3Count 0.05-5%.
The purpose of this invention is to provide the method for a kind of iron, chromium, molybdenum co-precipitation system-carbonoxide transformation catalyst, compare with the mixed grind method, prepared catalyst has active high, and intensity is good, is difficult for advantages such as efflorescence and long service life.
The objective of the invention is to adopt following method to realize, select the soluble inorganic salt (chromium can be used chromic anhydride) of a kind of iron, a kind of chromium to be made into mixed aqueous solution, the alkaline solution (NaOH or potassium hydroxide solution) that adds a kind of soluble molybdenum hydrochlorate in its solution, make iron, chromium, molybdenum co-precipitation, after then sediment fully being washed, filtration drying adds an amount of potassium hydroxide aqueous solution and grinds even back 400-500 ℃ of roasting 2 hours, plays the sheet moulding again.
Concrete measure is (as FeCl with soluble ferric iron salt
3, Fe(NO
3)
3, Fe
2(SO
4)
3, Fe(AC)
3Deng) with the solubility chromic salts (as CrCl
3, Cr(NO
3)
3, Cr
2(SO
4)
3, Cr(AC)
3Deng) the aqueous solution and the alkaline solution of soluble molybdenum hydrochlorate (as potassium molybdate, sodium molybdate, ammonium molybdate etc.) mix, generate the co-precipitation of iron molybdate, molybdic acid chromium, iron hydroxide and chromium hydroxide, also can be in soluble ferrite (as FeSO
4, Fe(NO
3)
2Deng) alkaline solution that adds in the aqueous solution behind the chromic anhydride again with soluble molybdenum hydrochlorate (as potassium molybdate, sodium molybdate, ammonium molybdate etc.) mixes, generate the co-precipitation of iron molybdate, molybdic acid chromium, iron hydroxide and chromium hydroxide, coprecipitate is carried out above-mentioned washing, filtration, drying, roasting and moulding.
The experiment active testing proves that its iron content is with Fe
2O
3Count 60-90%, 75-85% more preferably, chromium content is with Cr
2O
3Count 5-10%, 6.8-7.6% more preferably, molybdenum content is with MoO
3Count 0.01-5%, more preferably 0.5-1%.
Because the primary accelerator MoO of catalyst
3Be to mix, compared, increased greatly the decentralization and the uniformity of Mo component, thereby improve the active and anti-efflorescence ability of its transformationreation with solid mixed grind method with the same iron of co-precipitation form, chromated oxide.
The activity of such catalysts test is carried out under normal pressure, and granularity is the 6-8 order, and tube inner diameter is 32mm, and bed volume is 30ml, and the dry gas air speed is 500 o'clock
-1, steam-to-gas ratio is 0.5, semiwater gas (CO-30.5%, CO
2-6.5%), temperature is 350 ℃, and property work is represented with the CO interconversion rate.
Embodiment 1
Get (NH
4)
2MoO
41g(or Na
2MoO
41.05g, K
2MoO
41.22g), NaOH10g is dissolved in and is mixed with 1 ° of solution in the 20ml water, gets Fe
2(SO
4)
350g(or FeCl
340g, Fe(NO
3)
360g) be dissolved in and add 1 ° of solution in the 200ml water while stirring, abundant washing precipitate, dry back adds 20%KOH1ml, grinds all the back and plays the sheet moulding then 400-500 ℃ of following roasting 2 hours.Adopt above-mentioned test condition to record active numerical value and see Table 1
Table 1
| Method for preparing catalyst | Solid mixed grind * | Co-precipitation |
| Active (CO conversion ratio) | 75.0% | 81.9% |
* in the solid mixed grind method, component content such as its Fe, Cr, Mo are identical with coprecipitation method
Embodiment 2
Get FeSO
460g(or Fe(NO
3)
272g) be dissolved in the 150ml water, add chromic anhydride 6g dissolving, add while stirring among the embodiment 11 ° of solution to precipitation fully, abundant washing precipitate, dry back adds 20%KOH1ml, grinds all the back and plays the sheet moulding then 400-500 ℃ of following roasting 2 hours.Adopt above-mentioned test condition to record active numerical value and see Table 2.
Table 2
| Method for preparing catalyst | Solid mixed grind * | Co-precipitation |
| Active (CO conversion ratio) | 78.0% | 84.4% |
* component content such as its Fe, Cr, Mo are identical with coprecipitation method in the solid mixed grind method
Claims (3)
1, a kind of preparation method of Fe-Cr-Mo series carbon monoxide medium temperature shift catalyst, feature is to select the soluble inorganic salt of a kind of iron, a kind of chromium (chromium can be used chromic anhydride) to be made into mixed aqueous solution, the alkaline solution (NaOH or potassium hydroxide solution) that adds a kind of soluble molybdenum hydrochlorate in its solution, make iron, chromium, molybdenum co-precipitation, after then sediment fully being washed, filtration drying, add an amount of potassium hydroxide aqueous solution stone roller and all play the sheet moulding again 400-500 ℃ of following roasting 2 hours in the back.
2, the method for claim 1 is characterized in that iron, chromium, molybdenum co-precipitation employing are selected from FeCl
3, Fe(NO
3)
3, Fe
2(SO
4)
3, Fe(AC)
3In a kind of aqueous solution with being selected from CrCl
3, Cr(NO
3)
3, Cr
2(SO
4)
2, Cr(AC)
3In a kind of aqueous solution be selected from alkaline solution a kind of in potassium molybdate, sodium molybdate, the ammonium molybdate and mix, generate the co-precipitation of iron molybdate, molybdic acid chromium, iron hydroxide and chromium hydroxide.
3, method as claimed in claim 1, the co-precipitation that it is characterized in that iron, chromium, molybdenum is to select FeSO
4, Fe(NO
3)
2In a kind of aqueous solution, mix with being selected from alkaline solution a kind of in potassium molybdate, sodium molybdate, the ammonium molybdate again after adding chromic anhydride, generate the co-precipitation of iron molybdate, molybdic acid chromium, iron hydroxide and chromium hydroxide.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 90101486 CN1018795B (en) | 1990-03-17 | 1990-03-17 | Process for preparing fe-cr-mo system catalysts for co transform |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 90101486 CN1018795B (en) | 1990-03-17 | 1990-03-17 | Process for preparing fe-cr-mo system catalysts for co transform |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1045359A true CN1045359A (en) | 1990-09-19 |
| CN1018795B CN1018795B (en) | 1992-10-28 |
Family
ID=4877086
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 90101486 Expired CN1018795B (en) | 1990-03-17 | 1990-03-17 | Process for preparing fe-cr-mo system catalysts for co transform |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1018795B (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1050151C (en) * | 1997-12-23 | 2000-03-08 | 石油大学(华东) | Cataluyst for slag oil suspension bed hydrogen cracking |
| CN1064991C (en) * | 1997-05-07 | 2001-04-25 | 中国石化齐鲁石油化工公司 | Conversion process for dry gas purification and purifying agent thereof |
| CN1065153C (en) * | 1994-12-06 | 2001-05-02 | 四川川化集团公司催化剂厂 | High temp. changing catalyst and its preparing method |
| CN101491763B (en) * | 2008-12-24 | 2011-11-16 | 湖北双雄催化剂有限公司 | Preparation method capable of increasing sulfur tolerance of middle temperature iron-chromium shift catalyst using high-purity nano molybdenum trioxide |
| CN103119182A (en) * | 2010-08-16 | 2013-05-22 | 雪佛龙美国公司 | Process for separating and recovering metals |
| CN107946608A (en) * | 2017-11-20 | 2018-04-20 | 郑州天舜电子技术有限公司 | A kind of fuel cell low cost catalyst and preparation method thereof |
| CN114797884A (en) * | 2022-05-19 | 2022-07-29 | 四川鸿鹏新材料有限公司 | Catalyst for vinylene carbonate production, preparation method and application |
-
1990
- 1990-03-17 CN CN 90101486 patent/CN1018795B/en not_active Expired
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1065153C (en) * | 1994-12-06 | 2001-05-02 | 四川川化集团公司催化剂厂 | High temp. changing catalyst and its preparing method |
| CN1064991C (en) * | 1997-05-07 | 2001-04-25 | 中国石化齐鲁石油化工公司 | Conversion process for dry gas purification and purifying agent thereof |
| CN1050151C (en) * | 1997-12-23 | 2000-03-08 | 石油大学(华东) | Cataluyst for slag oil suspension bed hydrogen cracking |
| CN101491763B (en) * | 2008-12-24 | 2011-11-16 | 湖北双雄催化剂有限公司 | Preparation method capable of increasing sulfur tolerance of middle temperature iron-chromium shift catalyst using high-purity nano molybdenum trioxide |
| CN103119182A (en) * | 2010-08-16 | 2013-05-22 | 雪佛龙美国公司 | Process for separating and recovering metals |
| CN107946608A (en) * | 2017-11-20 | 2018-04-20 | 郑州天舜电子技术有限公司 | A kind of fuel cell low cost catalyst and preparation method thereof |
| CN114797884A (en) * | 2022-05-19 | 2022-07-29 | 四川鸿鹏新材料有限公司 | Catalyst for vinylene carbonate production, preparation method and application |
| CN114797884B (en) * | 2022-05-19 | 2023-05-09 | 四川鸿鹏新材料有限公司 | Catalyst for producing vinylene carbonate, preparation method and application |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1018795B (en) | 1992-10-28 |
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