CN1810793A - Furaldehyde-degrading cooperative ultrasomic wave and nanometer TiO2 method - Google Patents
Furaldehyde-degrading cooperative ultrasomic wave and nanometer TiO2 method Download PDFInfo
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- CN1810793A CN1810793A CN 200610033961 CN200610033961A CN1810793A CN 1810793 A CN1810793 A CN 1810793A CN 200610033961 CN200610033961 CN 200610033961 CN 200610033961 A CN200610033961 A CN 200610033961A CN 1810793 A CN1810793 A CN 1810793A
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- furfural
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- furaldehyde
- tio
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Abstract
The present invention is synergistic furaldehyde-degrading ultrasonic wave and nanometer TiO2 method. The method features that nanometer TiO2 is first dispersed inside furaldehyde solution or loaded on carrier and suspended inside furaldehyde solution, and H2O2 solution is added; and the furaldehyde solution is then ultrasonic treated for being degraded into harmless CO2 and water. The method of the present invention can decarbonylate furaldehyde in 60 min and degrade furaldehyde into harmless CO2 and water in 3 hr, and has excellent application foreground in degrading waste water containing toxic furaldehyde and other harmful compound.
Description
Technical field
The present invention relates to a kind of degradation method of furfural, relate to a kind of ultrasonic synergistic nano-TiO specifically
2The method of degraded furfural.
Background technology
Ultrasonic wave can produce some extreme conditions in the medium that chemical reaction is used always, produce ultrahigh-temperature and the ultra-high voltage of local and moment, this energy not only can excite, induce many chemical reactions, accelerate chemical reaction velocity, even can change some chemical reaction direction, produce beyond thought effect.The Maitsev of USSR (Union of Soviet Socialist Republics) has early studied the influence of ultrasonic wave to heterogeneous catalysis process, finds that ultrasonic energy makes per pass conversion improve nearly 10 times, and its reason has thought to increase the dispersity of catalyzer.In recent years, Han etc. has investigated low intensity ultrasound (≤10W/cm
2) effect Reformatsky reaction down, find that reaction yield reaches more than 90% behind ultrasonic 30min, the more important thing is and needn't prepare zinc powder by the reduction Zinc Chloride Anhydrous again with high activity, also needn't re-use trimethylammonium boric acid.Suclick etc. are 50W/cm at the sound intensity also
2Studied this reaction under the condition, found that in the time of 25 ℃ behind the ultrasonic 5min of this mixture, productive rate can reach more than 95%, find simultaneously promotor at this to productive rate and reaction times did not influence.As everyone knows, common nickel powder is very poor to the catalytic activity of olefin hydrogenation, generally all be difficult to carry out at 300h left and right sides afterreaction.But behind the ultrasonication nickel powder, react very fast startup, its speed of reaction increases with the prolongation of supersound process time earlier, after reduce gradually again.Suslick etc. have studied the hydrogenation reaction of nickel powder as catalyzer in great detail, find that its reactive behavior has improved 5 orders of magnitude under ultrasonication.Ronmy and Price etc. have studied the alkyl oil of mirbane automatic oxidation reaction in the phase transition base catalysis, find that speed of response significantly rises under ultrasonication, and the reaction times shortens 2h, and the selectivity of acid significantly improves, and have a large amount of nitrobenzoic acids to generate in the product.In addition, ultrasonic wave also demonstrates special advantages in activation, regeneration and the preparation of catalyzer.Illinois, US university succeeds in developing a kind of ultrasonic washing and bathes, and can be used for removing the oxide film on nickel powder surface, makes the nickel catalyzator activation.The Henry of U.S. Exxon company report can make the nickel-molybdenum catalyst of the lasting inactivation of hydrocracking use be regenerated with ultrasonic wave.Recently, Suslick etc. studies Fe (Co) under ultrasonication
5And Co (CO)
3Interaction find: forming nano level Fe-Co alloy catalyst under strong ultrasonication, its dehydrogenation to hexanaphthene is separated has very high activity.In the ultrasonic wave homogeneous catalytic reaction, studying more is the olefin isomerization of metal carbonyl as catalyzer.The Suclick of Northwestern Univ USA etc. has studied in great detail under the ultrasound condition with Fe (Co)
5For the 1-amylene isomerization of catalyzer generates the reaction of 2-amylene, find under the ultrasound condition the speed of reaction ratio do not have to have increased by 105 times when ultrasonic.Analyses such as Suclik think that the High Temperature High Pressure that produces during the collapse of ultrasonic cavitation bubble and the quick cooling of surrounding environment help Fe (CO)
5Dissociate, form more high reactivity species Fe
3(CO)
12
Because the ultrasonic wave catalyzed reaction is a new research field, the researchist still has different opinion to its mechanism of action in the industry.The principle that generally believes the ultrasonic wave catalyzed reaction mainly contains:
(1) produces High Temperature High Pressure and make reactant be cracked into free radical and dicovalent carbon, form more active reaction species;
(2) shockwave and microjet produce desorb and cleanup action, cleaning reaction product or intermediate and catalyst surface passivation layer to solid surface (as catalyzer);
(3) shockwave destroys the reactant structure;
(4) shockwave disperses the reaction system;
(5) ultrasonic cavitation corrosion catalyst surface, shockwave cause the distortion of catalyst crystal lattice and the formation of internal strain district (structural aberration), thereby improve chemical reactivity;
(6) shockwave impels solvent to be deep into solid interior, produces the so-called reaction that is mingled with;
(7) shockwave has improved the catalyzer dispersiveness.
Rising in recent years is handled organic waste water with the heterogeneous photocatalysis technology of semi-conductor.In numerous conductor photocatalysis materials, TiO
2Gain great popularity with catalytic efficiency is high because of its chemical property is stable.Under the irradiation of UV-light, TiO
2With H
2O produces the OH free radical with extremely strong oxidation capacity, finally can make organic pollutant be degraded to CO fully
2, H
2O and some simple mineral ions.But UV-light is very low to the penetrativity of nontransparent material, adds TiO with rayed
2When handling the very low sewage of muddiness or transparency, the utilization ratio of light is very low.Therefore use ultrasonic synergistic TiO
2Catalyzed reaction provide a new method to degradable organic pollutant with broad prospect of application.Some complicated compounds are by ultrasonic wave combining nano TiO
2Successfully obtain degraded, comprising 2,3,4-Trichlorophenol, phenol, 2-chlorophenol, 3-chlorophenol etc.
Furfural is a furtural, be important organic chemical industry's solvent and raw materials for production, can be used for producing synthon, synthetic rubber, plastics, foundry resin, medicine, agricultural chemicals, fuel, spices etc., also is deep processing of farm products, the leading industry of increasing peasant income, foreign exchange earning.But for many years, the sewage disposal of furfural is to hinder the bottleneck that this industry develops in a healthy way always.The furfural treatment process that existing patent is reported is the separation of mixture mostly, and the nothing that yet there are no success so far poisons, the report of recycling processing method.
Summary of the invention
The objective of the invention is to develop a kind of nontoxic ultrasonic synergistic nano-TiO
2The method of degraded furfural.
We are with nano-TiO
2Homodisperse is suspended in the furfural solution, or loads on silica glass microballon, fiber spring, Microcrystalline Cellulose, activated carbon fiber or the online resuspending of Stainless Steel Wire in furfural solution, adds H again
2O
2, adopt power ultrasonic to handle then, make furfural be degraded to furancarboxylic acid, furans, maleic acid, carbonic acid gas and water until carbonic acid gas that is converted into toxicological harmless fully and water, thereby are realized purpose of the present invention.
The method of a kind of furfural of degrading of the present invention is characterized in that comprising the steps:
(1) with nano-TiO
2Homodisperse is suspended in the furfural solution, or with nano-TiO
2Load on the carrier resuspending in furfural solution;
(2) in furfural solution, add H
2O
2Solution is 12～25W/cm at 35～65 ℃ with power density
3Ultrasonication furfural solution, make furfural be degraded to CO
2And H
2O.
The described nano-TiO of step (1)
2Consumption be that every 200mL furfural solution adds 0.05～0.15g, described nano-TiO
2Anatase titanium dioxide torispherical preferably, described carrier can be silica glass microballon, fiber spring, Microcrystalline Cellulose, activated carbon fiber or Stainless Steel Cloth etc.
The described H of step (2)
2O
2The consumption of solution is that every 200mL furfural solution adds 8～20mL, H
2O
2The concentration of solution can be 20mg/L, and reaction can be in pH=5.5～11 time be carried out, and described frequency of ultrasonic can be 18.5～22KHz or 18.5～22KHz and 30～45KHz mixing.
Method of the present invention can have been finished in 60min usually at 410～415 ℃, ZnO/Cr
2O
3/ MnO
2The decarbonylation reaction of the furfural that catalysis could realize down, and in 3h, furfural is degraded to fully the CO of toxicological harmless
2And H
2O.And the present invention is with nano-TiO
2Be applied to catalytic field, and need not UV-light and high temperature and composite catalyst system causes, better effects has been arranged for the colored heterocycle, aldehyde, the toxic waste water of phenols of containing of degraded furfural class.And with nano-TiO
2Be carried on the carrier, no nanoparticle is brought in the liquid phase of discharge, the secondary environmental pollution of having avoided nanoparticle to cause.
Embodiment
Following examples are to further specify of the present invention, are not limitations of the present invention.
Embodiment 1:
With 0.05g anatase titanium dioxide torispherical nano-TiO
2Homodisperse is suspended in the furfural aqueous solution that 200mL concentration is 20mg/L, and adding concentration is the H of 20mg/L
2O
2Aqueous solution 8mL, regulating pH is 8, under 45 ℃, carry out power ultrasonic and handle, timing sampling, the centrifuging and taking supernatant liquid, and carry out ultraviolet-visible (UV-Visible) spectrometry and follow analysis, measure the variation of furfural content and the variation of solution UV absorption peak.The result shows that working as ultrasonic frequency is that 18.5KHz, power density are 12W/cm
3The time, 60min has removed carbonyl, and 45% furfural has been converted into CO during 120min
2And H
2O.And work as power density is 20W/cm
3The time, 30min has removed carbonyl, and 160min is converted into CO fully with furfural
2And H
2O.
Embodiment 2:
With 0.15g anatase titanium dioxide torispherical nano-TiO
2Homodisperse is suspended in the furfural aqueous solution that 200mL concentration is 20mg/L, and adding concentration is the H of 20mg/L
2O
2Aqueous solution 15mL, regulating pH is 7, under 40 ℃, carry out power ultrasonic and handle, timing sampling, the centrifuging and taking supernatant liquid, and carry out ultraviolet-visible (UV-Visible) spectrometry and follow analysis, measure the variation of furfural content and the variation of solution UV absorption peak.The result shows that working as ultrasonic frequency is 20KHz and 30KHz hybrid frequency, and phasic difference focuses on, and power density is 25W/cm
3The time, 30min has removed carbonyl, and 160min is converted into CO fully with furfural
2And H
2O.Contrast under the identical situation of other conditions, no nano-TiO
2Participate in catalyzed reaction, even then after handling 180min, still carbonyl can't be removed fully, furfural also only has 60% to be converted into CO
2And H
2O.
Embodiment 3:
With 0.10g anatase titanium dioxide torispherical nano-TiO
2Load on the 15g silica glass microballon (apparent mean diameter is 0.5mm), homodisperse is suspended in the furfural aqueous solution that 200mL concentration is 20mg/L under stirring at low speed, and adding concentration is the H of 20mg/L
2O
2Aqueous solution 20mL, regulating pH is 5.5, carries out power ultrasonic and handle timing sampling under 35 ℃.Sedimentation easily, centrifugation.Get supernatant liquid, and carry out ultraviolet-visible (UV-Visible) spectrometry and follow analysis, measure the variation of furfural content and the variation of solution UV absorption peak.The result shows that working as ultrasonic frequency is 22KHz and 40KHz hybrid frequency, and phasic difference focuses on, and power density is 25W/cm
3The time, 30min has removed carbonyl, furfural is converted into CO fully during 120min
2And H
2O.
Embodiment 4:
With 0.15g anatase titanium dioxide torispherical nano-TiO
2Load on the 15g microcrystalline cellulose crude granule on (apparent mean diameter is 80 μ m), homodisperse is suspended in the furfural aqueous solution that 200mL concentration is 20mg/L under stirring at low speed, and adding concentration is the H of 20mg/L
2O
2Aqueous solution 15mL, regulating pH is 11, carries out power ultrasonic and handle timing sampling under 65 ℃.Sedimentation easily, centrifugation.Get supernatant liquid, and carry out ultraviolet-visible (UV-Visible) spectrometry and follow analysis, measure the variation of furfural content and the variation of solution UV absorption peak.The result shows that working as ultrasonic frequency is 22KHz and 45KHz hybrid frequency, and phasic difference focuses on, and power density is 25W/cm
3The time, 30min has removed carbonyl, furfural is converted into CO fully during 120min
2And H
2O.
Embodiment 5:
With 0.15g anatase titanium dioxide torispherical nano-TiO
2Load on the bedspring laminar surface that quartz glass fibre turns to, hang in the furfural aqueous solution that 200mL concentration is 20mg/L, adding concentration is the H of 20mg/L
2O
2Aqueous solution 15mL, regulating pH is 7, carries out power ultrasonic and handle timing sampling under 40 ℃.Draw clear liquid, and carry out ultraviolet-visible (UV-Visible) spectrometry and follow analysis, measure the variation of furfural content and the variation of solution UV absorption peak.The result shows that working as ultrasonic frequency is 22KHz and 40KHz hybrid frequency, and phasic difference focuses on, and power density is 25W/cm
3The time, 30min has removed carbonyl, furfural is converted into CO fully during 120min
2And H
2O.
Claims (3)
1. the method for the furfural of degrading is characterized in that comprising the steps:
(1) with nano-TiO
2Homodisperse is suspended in the furfural solution, or with nano-TiO
2Load on the carrier resuspending in furfural solution;
(2) in furfural solution, add H
2O
2Solution 2 is 12～25W/cm at 35～65 ℃ with power density
3Ultrasonication furfural solution, make furfural be degraded to CO
2And H
2O.
2. according to the method for claim 1 furfural of degrading, it is characterized in that the described nano-TiO of step (1)
2Consumption be that every 200mL furfural solution adds 0.05～0.15g, described nano-TiO
2Be the anatase titanium dioxide torispherical, described carrier is silica glass microballon, fiber spring, Microcrystalline Cellulose, activated carbon fiber or Stainless Steel Cloth.
3. according to the method for claim 1 or 2 one kind of furfural of degrading, it is characterized in that the described H of step (2)
2O
2The consumption of solution is that every 200mL furfural solution adds 8～20mL, H
2O
2The concentration of solution is 20mg/L, and reaction can be in pH=5.5～11 time be carried out, and described frequency of ultrasonic is 18.5～22KHz or 18.5～22KHz and 30～45KHz mixing.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100339618A CN100361986C (en) | 2006-03-01 | 2006-03-01 | Furaldehyde-degrading cooperative ultrasomic wave and nanometer TiO2 method |
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|---|---|---|---|
| CNB2006100339618A CN100361986C (en) | 2006-03-01 | 2006-03-01 | Furaldehyde-degrading cooperative ultrasomic wave and nanometer TiO2 method |
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| CN1810793A true CN1810793A (en) | 2006-08-02 |
| CN100361986C CN100361986C (en) | 2008-01-16 |
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|---|---|---|---|
| CNB2006100339618A Expired - Fee Related CN100361986C (en) | 2006-03-01 | 2006-03-01 | Furaldehyde-degrading cooperative ultrasomic wave and nanometer TiO2 method |
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Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1504308A (en) * | 1975-05-14 | 1978-03-15 | British Petroleum Co | Solvent extraction |
| DE3210911C2 (en) * | 1982-03-25 | 1985-10-31 | Kernforschungsanlage Jülich GmbH, 5170 Jülich | Process for obtaining furfural-degrading bacteria, bacteria obtainable thereafter and their use |
| DE3345691C2 (en) * | 1982-12-20 | 1986-08-07 | Kernforschungsanlage Jülich GmbH, 5170 Jülich | Process for the continuous anaerobic degradation of organic compounds |
| CN1629151A (en) * | 2004-10-09 | 2005-06-22 | 刘显臣 | Process waste water discharging free method for the production of furfural |
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2006
- 2006-03-01 CN CNB2006100339618A patent/CN100361986C/en not_active Expired - Fee Related
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