CN1739853A - Composite oxide solid acid catalyst and its prepn process - Google Patents
Composite oxide solid acid catalyst and its prepn process Download PDFInfo
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- CN1739853A CN1739853A CNA2005100413950A CN200510041395A CN1739853A CN 1739853 A CN1739853 A CN 1739853A CN A2005100413950 A CNA2005100413950 A CN A2005100413950A CN 200510041395 A CN200510041395 A CN 200510041395A CN 1739853 A CN1739853 A CN 1739853A
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- catalyst
- flyash
- ferrous sulfate
- filter cake
- sulfuric acid
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Abstract
The composite oxide solid acid catalyst is prepared with flyash and ferrous sulfate slag from titanium white powder plant as main material, and through activation, co-precipitation zirconium chloroxide, soaking with sulfuric acid, filtering, drying, high temperature roasting and other steps. The catalyst is applied in esterification, and has excellent catalytic effect, high catalytic activity, low cost, capacity of repeated use, and other features.
Description
Technical field
The invention belongs to solid catalyst preparation and applied technical field, be specifically related to a kind of composite oxide solid acid catalyst that is used for esterification and preparation method thereof.
Background technology
At present, trade waste---the flyash major applications also has by chemical method effective component extracting aluminium oxide in construction material brickmaking, concrete or filler etc.But its added value of the product that these methods make is not high, and there is secondary pollution in chemical method.Catalyst is made in corrosive liquids acid (as sulfuric acid, phosphoric acid, Hydrogen fluoric acid etc.) commonly used in organic synthesis and fine chemicals are synthetic, in recent years, people attempt to adopt solid super-strong acid to substitute liquid acid catalyst, but because there is main shortcoming in solid super-strong acid is the preparation cost height, the cost performance of catalyst is lower, has influenced the industrial applications of the alternative caustic acid of solid acid catalyst.As the preparation method of Chinese patent CH1075900 ultra-strong acid of oxide system, be that to adopt water content be that the solvent that the ethanol water of the heavy % of 1-99 is made zirconates prepares group VIII noble metals SO
4 2-/ ZrO
2The system super acids.Still there is complicated process of preparation in the super acids of this method preparation, and cost of material is higher; " petrochemical industry ", 2004,33 (4): the disclosed flyash composite solid-acid catalyst of 360-363, obtained good effect in the applied catalysis synthesizing adipic acid di-n-octyl, but Preparation of catalysts still needs more zirconium oxychloride, cost is higher.
Summary of the invention
The object of the present invention is to provide a kind of is composite solid-acid catalyst of producing of primary raw material and preparation method thereof with flyash, ferrous sulfate etc.
Composite oxide solid acid catalyst of the present invention is mainly mixed by a certain percentage by flyash, ferrous sulfate, zirconium oxychloride and sulfuric acid.Because trade waste---the main component of flyash is silica, aluminium oxide, iron oxide etc., and generally its oxide activity is very low, be difficult to chemical reaction takes place, have only by just making full use of after activating.The present invention adopts and with ferrous sulfate, carbonate and NaOH flyash is activated earlier, utilizes the footpath roasting under the sulfuric acid soaking conditions of silica, aluminium oxide, iron oxide and zirconia to make composite oxide solid acid catalyst again.
This catalyst mainly is prepared from by flyash, ferrous sulfate, zirconium oxychloride, sulfuric acid and NaOH, and wherein each raw material is respectively according to the mass fraction: 100 parts in flyash, ferrous sulfate 20-30 part, carbonate 2-5 part, zirconium oxychloride 10-20 part, sulfuric acid 2-3, NaOH 1.5-2.5 part.
Concrete preparation method is as follows:
(1) activation of flyash
The flyash and ferrous sulfate, the carbonate that take by weighing ormal weight fully mix, roasting 30min under 400 ℃ of conditions, and taking out the back, to add concentration be the sodium hydroxide solution of 1.5～2.5mol/L, filters to get filtrate and filter residue after leaving standstill 2h;
(2) co-precipitation
The filtrate that makes is transferred pH ≈ 9 with 30% sulfuric acid, add the zirconium oxychloride (ZrOCl of ormal weight again
28H
2O) stir, transfer pH=8～9, filter behind ageing 8～12h, wash, until no Cl with concentrated ammonia liquor
-Till the existence, obtain filter cake a; With the filter residue that makes and the zirconium oxychloride (ZrOCl of ormal weight
28H
2O) mix,, transfer pH to 8～9 with ammoniacal liquor again, filter behind ageing 8～12h, wash, until no Cl with water-soluble the separating of 4 times in flyash
-Till the existence, obtain filter cake b;
(3) acidleach, drying and roasting
The dry 12h under 110 ℃ of conditions with filter cake a or filter cake b, sulfuric acid with 0.25/L soaks 2h then, again after filtration, dry, porphyrize roasting 3h under 550 ℃ of conditions just gets solid acid catalyst, wherein the catalyst that is made by filter cake a is an A type catalyst, and the catalyst that is made by filter cake b is the Type B catalyst.
Wherein carbonate is sodium acid carbonate or carbonic hydroammonium, and ferrous sulfate is the industrial raw material or the by-product ferrous sulfate during of titanium powder plant.
Prepared A type catalyst is applied in butyl butyrate synthetic respond well, it is higher that the Type B catalyst is applied in the preparation of dioctyl adipate esterification yield, and catalyst can also be reused.Concrete catalytic reaction is as follows:
1, the preparation method of butyl butyrate
In being furnished with the 100ml three-necked bottle of thermometer, water knockout drum and reflux condensing tube, add n-butyric acie (0.2mol) 18.40ml, n-butanol (0.4mol) 36.80ml by certain mol proportion, with a certain amount of catalyst and band aqua, add hot reflux, divide water, carry out esterification.Behind the reaction certain hour, sampling detecting acid number, the water yield in water knockout drum no longer increases, and the feature heating finishes reaction.Esterification yield is surveyed in sampling.
2, the preparation method of the positive dioctyl ester of adipic acid
In the there-necked flask that thermometer, reflux condensing tube, water knockout drum and electric mixer are housed, add a certain amount of adipic acid, n-octyl alcohol and band aqua.Heating under agitation earlier makes the adipic acid dissolving, with the pipette sampling, adds a certain amount of solid acid catalyst then, the control reaction temperature is carried out reflux water-dividing 150-160 ℃ of scope, appears as until the no globule and ends, stop heating, esterification yield is surveyed in sampling, presses GB1668-81 assay method esterification yield.
Because adopting with flyash is raw material and through the effect that ferrous sulfate and carbonate activate, and the active ingredient in the flyash is fully utilized, and can form the complex solid acid site under sulfuric acid, existing L acid position has the effect of B acid again in the molecule.Be applied to all have good catalytic effect in Lewis acid and the Bronsted acid catalytic reaction.In addition, owing to utilized trade waste---flyash and ferrous sulfate, the cost of catalyst is reduced greatly, the repeatability of catalyst and stability obviously improve, compare with the solid acid of present preparation, the catalyst performance price of not inventing is than significantly increasing, and having alternative fully corrosive liquids acid is possibility of its application in industry.
The specific embodiment
Embodiment 1
(1), take by weighing flyash and the 20g ferrous sulfate of 100g, 2g carbonic hydroammonium fully mixes, roasting 30min under 400 ℃ of conditions takes out the back and adds 2.5g NaOH, concentration is 1.5mol/L, filters to get filtrate and filter residue after leaving standstill 2h;
(2) filtrate that makes is transferred pH ≈ 9 with 30% sulfuric acid, add the zirconium oxychloride (ZrOCl of 20g again
28H
2O) stir, transfer pH=8～9, filter behind the ageing 12h, wash, until no Cl with concentrated ammonia liquor
-Till the existence, obtain filter cake a
1
(3) with filter cake a
1Dry 24h under 110 ℃ of conditions soaks 2h with the sulfuric acid that 3g sulfuric acid is made into 0.25mol/L then, more after filtration, dry, porphyrize roasting 3h under 550 ℃ of conditions just makes solid acid catalyst A1.
Embodiment 2
(1), take by weighing flyash and the 30g ferrous sulfate of 100g, 5g carbonic hydroammonium fully mixes, roasting 30min under 400 ℃ of conditions takes out the back and adds 1.5g NaOH, concentration is 2.5mol/L, filters to get filtrate and filter residue after leaving standstill 2h;
Step (2) and (3) make solid acid catalyst A2 with embodiment 1 method.
Embodiment 3
(1), take by weighing flyash and the 30g ferrous sulfate of 100g, 5g carbonic hydroammonium fully mixes, roasting 30min under 400 ℃ of conditions takes out the back and adds 1.5g NaOH, concentration is 2.5mol/L, filters to get filtrate and filter residue after leaving standstill 2h;
(2) filtrate that makes is transferred pH ≈ 9 with 30% sulfuric acid, add the zirconium oxychloride (ZrOCl of 10g again
28H
2O) stir, transfer pH=8～9, filter behind the ageing 8h, wash, until no Cl with concentrated ammonia liquor
-Till the existence, obtain filter cake a
3
(3) with filter cake a
3Dry 24h under 110 ℃ of conditions soaks 2h with the sulfuric acid that 2g sulfuric acid is made into 0.25mol/L then, more after filtration, dry, porphyrize roasting 3h under 550 ℃ of conditions just makes solid acid catalyst A3.
Embodiment 4
(1), take by weighing flyash and the 30g ferrous sulfate of 100g, the 5g sodium acid carbonate fully mixes, roasting 30min under 400 ℃ of conditions takes out the back and adds 1.5g NaOH, concentration is 2.5mol/L, filters to get filtrate and filter residue after leaving standstill 2h;
Step (2) and (3) method make solid acid catalyst A4 with embodiment 3
Embodiment 5
(1), take by weighing flyash and the 20g ferrous sulfate of 100g, 2g carbonic hydroammonium fully mixes, roasting 30min under 400 ℃ of conditions takes out the back and adds 2.5g NaOH, concentration is 1.5mol/L, filters to get filtrate and filter residue after leaving standstill 2h;
(2) with the filter residue and the 20g zirconium oxychloride (ZrOCl that make
28H
2O) mix,, transfer pH to 8～9 with ammoniacal liquor again, filter behind the ageing 12h, wash, until no Cl with water-soluble the separating of 4 times in flyash
-Till the existence, obtain filter cake b
1
(3) with filter cake b
1Dry 24h under 110 ℃ of conditions soaks 2h with the sulfuric acid that 2g sulfuric acid is made into 0.25mol/L then, more after filtration, dry, porphyrize roasting 3h under 550 ℃ of conditions just makes solid acid catalyst B1.
Embodiment 6
(1), take by weighing flyash and the 30g ferrous sulfate of 100g, 5g carbonic hydroammonium fully mixes, roasting 30min under 400 ℃ of conditions takes out the back and adds 1.5g NaOH, concentration is 2.5mol/L, filters to get filtrate and filter residue after leaving standstill 2h;
Step (2) and (3) make solid acid catalyst B2 with embodiment 5 methods.
Embodiment 7
(1), take by weighing flyash and the 30g ferrous sulfate of 100g, 5g carbonic hydroammonium fully mixes, roasting 30min under 400 ℃ of conditions takes out the back and adds 1.5g NaOH, concentration is 2.5mol/L, filters to get filtrate and filter residue after leaving standstill 2h;
(2) with the filter residue and the 10g zirconium oxychloride (ZrOCl that make
28H
2O) mix,, transfer pH to 8～9 with ammoniacal liquor again, filter behind the ageing 12h, wash, until no Cl with water-soluble the separating of 4 times in flyash
-Till the existence, obtain filter cake b
3
(3) with filter cake b
3Dry 24h under 110 ℃ of conditions soaks 2h with the sulfuric acid that 3g sulfuric acid is made into 0.25mol/L then, more after filtration, dry, porphyrize roasting 3h under 550 ℃ of conditions just makes solid acid catalyst B3.
Embodiment 8
(1), take by weighing flyash and the 30g ferrous sulfate of 100g, the 5g sodium acid carbonate fully mixes, roasting 30min under 400 ℃ of conditions takes out the back and adds 2.5g NaOH, concentration is 2.5mol/L, filters to get filtrate and filter residue after leaving standstill 2h;
Step (2) and (3) method make solid acid catalyst B4 with embodiment 7
The catalyst of above embodiment preparation is applied in the esterification, and catalytic effect is seen basis 1:
Table 1 catalyst is in the influence of different esterifications to esterification yield
| The catalyst numbering | Esterification yield/% during butyl butyrate is synthetic | Esterification yield/% during the adipic acid n-octyl is synthetic |
| A1 A2 A3 A4 B1 B2 B3 B4 SO 4 2-/ZrO 2Dense H 2SO 4 | 95.3 95.9 94.6 95.6 86.4 86.3 86.1 87.2 85.2 89.2 | 86.7 89.1 88.6 89.0 98.2 97.6 98.4 98.5 81.6 83.4 |
By embodiment and table 1 as can be seen, with different catalyst respectively to butyl butyrate and dioctyl adipate, under identical synthesis technologic parameter condition, of the present invention from catalyst than the concentrated sulfuric acid and SO
4 2-/ ZrO
2Catalytic effect is all good, but A type Type B all has certain selectivity, and wherein A type catalyst is applied in butyl butyrate synthetic respond wellly, and it is higher that the Type B catalyst is applied in the preparation of dioctyl adipate esterification yield.In addition, the catalyst that above embodiment is prepared is applied in the esterification, can repeat practical 5 times, and its esterification yield still can reach 80%, illustrates that catalyst of the present invention has good reusability.
Claims (3)
1, a kind of composite oxide solid acid catalyst is characterized in that: this catalyst mainly is prepared from by flyash, ferrous sulfate, zirconium oxychloride, sulfuric acid and NaOH, and wherein each raw material is respectively according to the mass fraction:
100 parts in flyash, ferrous sulfate 20-30 part, carbonate 2-5 part, zirconium oxychloride 10-20 part, sulfuric acid 2-3, NaOH 1.5-2.5 part.
2,, it is characterized in that this preparation method carries out according to following steps according to the described Preparation of catalysts method of claim 1:
(1) activation of flyash
The flyash and ferrous sulfate, the carbonate that take by weighing ormal weight fully mix, roasting 30min under 400 ℃ of conditions, and taking out the back, to add concentration be the sodium hydroxide solution of 1.5～2.5mol/L, filters to get filtrate and filter residue after leaving standstill 2h;
(2) co-precipitation
The filtrate that makes is transferred pH ≈ 9 with 30% sulfuric acid, and the zirconium oxychloride that adds ormal weight again stirs, and transfers pH=8～9 with concentrated ammonia liquor, filters behind ageing 8～12h, washs, until no Cl
-Till the existence, obtain filter cake a; The filter residue that makes is mixed with the zirconium oxychloride of ormal weight,, transfer pH to 8～9 with ammoniacal liquor again, filter behind ageing 8～12h, wash, until no Cl with water-soluble the separating of 4 times in flyash
-Till the existence, obtain filter cake b;
(3) acidleach, drying and roasting
The dry 12h under 110 ℃ of conditions with filter cake a or filter cake b, sulfuric acid with 0.25/L soaks 2h then, again after filtration, dry, porphyrize roasting 3h under 550 ℃ of conditions just gets solid acid catalyst, wherein the catalyst that is made by filter cake a is an A type catalyst, and the catalyst that is made by filter cake b is the Type B catalyst.
3, preparation method according to claim 2 is characterized in that: carbonate is sodium acid carbonate or carbonic hydroammonium, and ferrous sulfate is the industrial raw material or the by-product ferrous sulfate during of titanium powder plant.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100413950A CN100344372C (en) | 2005-08-10 | 2005-08-10 | Composite oxide solid acid catalyst and its prepn process |
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|---|---|---|---|
| CNB2005100413950A CN100344372C (en) | 2005-08-10 | 2005-08-10 | Composite oxide solid acid catalyst and its prepn process |
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| Publication Number | Publication Date |
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| CN1739853A true CN1739853A (en) | 2006-03-01 |
| CN100344372C CN100344372C (en) | 2007-10-24 |
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|---|---|---|---|
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1788842B (en) * | 2005-11-29 | 2010-05-05 | 安徽工业大学 | Dechlorination catalyst for degrading waste PVC and its preparation method |
| CN102059129A (en) * | 2010-12-31 | 2011-05-18 | 河南省华鼎高分子合成树脂有限公司 | Solid super acid and application thereof in preparing 4,4'-diaminodiphenylmethane |
| CN102965204A (en) * | 2012-10-31 | 2013-03-13 | 潍坊金信达生物化工有限公司 | Method for preparing biodiesel with catalysis of fly ash solid acid catalyst |
| CN112889845A (en) * | 2020-12-22 | 2021-06-04 | 安徽稞馨环境科技有限公司 | Preparation and application of composite oxide solid acid air bactericide |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1157256C (en) * | 2000-05-11 | 2004-07-14 | 中国科学院成都有机化学研究所 | Solid acid with high selectivity and activity for esterification and its prpen. |
-
2005
- 2005-08-10 CN CNB2005100413950A patent/CN100344372C/en not_active Expired - Fee Related
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1788842B (en) * | 2005-11-29 | 2010-05-05 | 安徽工业大学 | Dechlorination catalyst for degrading waste PVC and its preparation method |
| CN102059129A (en) * | 2010-12-31 | 2011-05-18 | 河南省华鼎高分子合成树脂有限公司 | Solid super acid and application thereof in preparing 4,4'-diaminodiphenylmethane |
| CN102059129B (en) * | 2010-12-31 | 2012-07-11 | 河南省华鼎高分子合成树脂有限公司 | Solid super acid and application thereof in preparing 4,4'-diaminodiphenylmethane |
| CN102965204A (en) * | 2012-10-31 | 2013-03-13 | 潍坊金信达生物化工有限公司 | Method for preparing biodiesel with catalysis of fly ash solid acid catalyst |
| CN112889845A (en) * | 2020-12-22 | 2021-06-04 | 安徽稞馨环境科技有限公司 | Preparation and application of composite oxide solid acid air bactericide |
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| Publication number | Publication date |
|---|---|
| CN100344372C (en) | 2007-10-24 |
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