CN1458138A - Acidifying, distilling and extracting method for natural propionic acid and acetic acid of propionic bacteria fermentation liquid - Google Patents
Acidifying, distilling and extracting method for natural propionic acid and acetic acid of propionic bacteria fermentation liquid Download PDFInfo
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Abstract
The present invention belongs to the technology of evaporation and distillation treatment technology. The technological process includes the main steps of: acidifying the concentrated liquid with non-volatile acid via stirring to convert the salt of propionic acid and acetic acid into free acid; and decompression distillation to obtain distillate mixed water solution of propionic acid and acetic acid. It is preferably to perform alkali pre-treatment and decompression distillation before acidification. The present invention features that from the fermented propionic bacteria liquid, mixed water solution of propionic acid and acetic acid with high purity may be extracted, and the mixed water solution may be further produced into various side products. The present invention can reduce exhausted waste liquid and environmental pollution.
Description
Technical field
The invention belongs to evaporation, the distillation processing technology field of industrial effluent.
Background technology
China is to use bacterium acidi propionici fermentative production vitamins B
12Big country, contain propionic acid, acetate and so on VFA in the fermentative production waste liquid, also have compositions such as a large amount of ammonium salts, protein.Unprocessed or discharge in a large number without the fermented waste fluid of fully handling, not only polluted environment, and be waste precious resources.Only the waste liquid amount of Shijiazhuang two tame factories discharging every day just reaches 550 tons more than.This rich in natural resources if can be reclaimed the natural polypropylene that obtains, acetate and its esters market that will be widely used.
Aspect foodstuffs industry, propionic acid can be used as sanitas and the sweetener of beverage, soy sauce, edible oil, cheese, tobacco etc., and its calcium, sodium, zinc salt are generally as the sanitas of bread, cake, sausage and various broil food.Be widely used at present in phenylformic acid, Sorbic Acid, propionic acid and its esters of food antiseptic, the anti-mold effect of propionic acid is better than phenylformic acid below pH5 and its price is lower than Sorbic Acid, is one of ideal sanitas.Its calcium salt has stronger restraining effect to all kinds of moulds, Gram-positive bacillus, to causing that the Bacillus subtilus that food is clamminess and the Salmonella of food poisoning have significant inhibitory effect, the generation that prevents flavus and toxin thereof is had unique effect, is general in the world food and the Midew preventive for feed of world health and food and agricultural organization approval.
Aspect husbandry, third, acetate and ammonium salt thereof be mainly as mildew-resistant, sanitas and the nutrition-fortifying agent of animal-feed, as be used for the mildew-resistant that high humidity cereal and feed comprise hay, silage, effects such as the diseases prevention of feeding animals, growth encourage are very remarkable.In pesticide industry, propionic acid is used to produce propionyl chloride, and then produces weedicide Stam F-34, metaxanin, napropamide etc.
Propionic acid is mainly used in the preparation vitamins B as medicine intermediate
6, Naproxen Base, Tolperisone, Uniteston, Beclomethasone, fluticasone propionate etc.The third, acetate also is the precursor substance of macrolide antibiotic such as erythromycin fermentation, can significantly promote the antibiotic biosynthesizing of this class.The purposes of propionic acid is also very extensive in perfume industry, can be used to prepare spices such as fragrant camphor tree ester, geranyl propionate, benzyl propionate, isoamyl propionate.
The third, acetate still is broad-spectrum Organic Chemicals, can be used as synthetic herbicide, cellulose acetate propionate plastics, softening agent, weaving and rubber industry auxiliary agent, dyestuff, esters solvent.By third, the various ester classes of acetate synthetic can be used as the solvent of cellulose ester, ethers, various natural or synthetic resins, wherein propionic ester also can be used as the special solvent that sprays paint, the nonflammable and blast of this kind solvent, safety in utilization is good.By propionic acid, acetate and Mierocrystalline cellulose synthetic cellulose acetate propionate is a kind of have special biodegradability and nontoxic thermoplastic material, can be made into disposable health plastic goods and wrapping material, helps environment protection.Also can produce α-Lv Bingsuan, 2 with propionic acid, 2-diaminopropionic acid and α-bromo-propionic acid etc.
At present, propionic acid mainly is that raw material carries out chemical synthesis production with petrochemicals.Production method has: (1) lower hydrocarbon direct oxidation method: can coproduction formic acid when being raw material production acetate and propionic acid with the lower hydrocarbon, get final product after the separation propionic acid.This method cost of material is cheap, technical process is simple, but the composition complexity in the reaction solution, separating purifies must take special measure, invests bigger.(2) Lei Pofa: with ethene is raw material, and with carbon monoxide and water reaction, a step generates propionic acid under the nickle carbonoxide katalysis.This method requires high to high pressure reactor, seriously corroded.(3) propionic aldehyde oxidation style: adopt Manganese dipropionate as catalyzer, the catalyzed oxidation propionic aldehyde prepares propionic acid.Selecting suitable device and pipe material for use is that the propionic aldehyde oxidation style is produced the key issue in the propionic acid.(4) ethanol oxo synthesis: under High Temperature High Pressure, with the halogenide of boron trifluoride, tetracol phenixin, neutralized verdigris, manganese or aluminium, nickel, cobalt, iron and chromium, molybdenum, wolframic acid etc. is catalyzer, ethanol and carbon monoxide liquid phase reaction generate propionic acid in acidic medium, and the propionic acid yield is 72%.This method is at first adopted by du pont company, but owing to technological problemses such as equipment corrosion under speed of reaction, yield, catalyst attrition and the High Temperature High Pressure are outstanding, extensively promotes on industrial production so far.(5) vinylformic acid hydrogenation method: vinylformic acid is catalyzer with copper-palladium based compound at normal temperatures and pressures, and directly hydrogenation reaction makes propionic acid.This method technology is simple, and reaction conditions is also gentle, but because problems such as vinylformic acid price and source have limited its development.
In recent years because the raising up of world petroleum price causes the cost of chemical synthesis to rise, to have a pollution bigger for chemical synthesis simultaneously, shortcomings such as equipment requirements and operational condition harshness, thus promoted to produce the development of propionic acid research with the fermentation using propionibacterium method.Compare with chemical synthesis, fermentation method uses renewable resources to be raw material, the reaction conditions gentleness, and Product Safety is good.But the fermentation method productive rate is lower, and product separation extracts difficulty, and cost is also higher, and causes a large amount of contaminated wastewaters, thereby the industrialization of all still being unrealized both at home and abroad so far.
External propionic acid production mainly concentrates on country, the particularly U.S. and Germany such as the U.S., Germany, Britain, Japan, South Africa, has occupied the overwhelming majority of world market share.Domestic only have on a small quantity from wood distillation and light hydrocarbon oxidation prepare propionic acid by-product production in the acetate process, output can not be met the need of market far away, and a large amount of imports are all arranged every year.The yearly capacity of China's glacial acetic acid is about 1,000,000 tons, can satisfy domestic needs substantially.
Summary of the invention
The purpose of this invention is to provide a kind of natural polypropylene, acetate acidifying distillation extraction method of bacterium acidi propionici fermented liquid, be characterized in: can from the bacterium acidi propionici fermented liquid, comprise bacterium acidi propionici fermentative production vitamins B
12Extract natural polypropylene, acetic acid mixed aqueous solution in the waste liquid behind the separating thallus.And can further be processed into the mixture of their salt such as calcium, sodium, potassium, zinc, iron, byproducts such as also recyclable simultaneously ammonia, ammonium salt, secondary calcium phosphate or calcium sulfate.Its technology is simple, and third, the rate of recovery height of acetate, production cost is low, and good product quality can effectively reduce the discharging and the environmental pollution of fermented waste fluid, and be convenient to industrialization.
Technical scheme of the present invention is: a kind of natural polypropylene of bacterium acidi propionici fermented liquid, acetate acidifying distillation and extraction method is characterized in that the main following two step extraction process steps that adopt:
A, acidifying: the bacterium acidi propionici fermented liquid is regulated pH1.0～5.0 with non-volatile acid, fully stir, make fermentation useless
In the liquid third, acetate are converted into free acid by the form of ammonium salt or other salt;
B, underpressure distillation: acidizing fluid is carried out underpressure distillation, and distillate is natural polypropylene, acetic acid mixed aqueous solution.
Above-mentioned bacterium acidi propionici fermented liquid comprises the anaerobic fermented liquid of various bacterium acidi propionicis, also can be that the bacterium acidi propionici anaerobically fermenting is produced vitamins B
12Waste liquid behind the separating thallus.
The acidifying pH of above-mentioned acidizing process is good with 2.5～3.5, both can make third, acetate all dissociates out, can alleviate the corrosion to equipment again.
In order further to improve the purity and the recovery rate of gained third, acetic acid mixed aqueous solution, be preferably in preceding fermented liquid alkalescence pre-treatment and two step of the reduction vaporization operation of adding of above-mentioned processing step.So processing step can be transformed into following four steps:
A, alkaline pre-treatment: add calcium oxide or calcium hydroxide, regulate bacterium acidi propionici fermented liquid pH7.5～10.5, make and send out
Protein flocculation in the ferment liquid can be used as feed or feed B after the filter residue and drying that filtration obtains
12Weighting agent,
Filtrate enters next step abstraction process;
B, reduction vaporization: above-mentioned filtrate is carried out reduction vaporization, remove ammonia and other alkalescence and neutral in the fermented liquid
The volatility meta-bolites, and make filtrate concentrated;
C, acidifying: decompressed concentrate is regulated pH1.0～5.0 with non-volatile acid, fully stir, make fermented waste fluid
In third, acetate is converted into free acid by the form of ammonium salt or other salt;
D, underpressure distillation: acidizing fluid is carried out underpressure distillation, and distillate is natural polypropylene, acetic acid mixed aqueous solution.
Above-mentioned alkaline pretreatment process adds calcium oxide or calcium hydroxide to carry out alkaline pretreated pH and is preferably 8.0～9.0, and purpose is to reach best flocculating effect, and the pH in the time of guaranteeing reduction vaporization again is not less than 6.0, avoids third, the volatilization loss of acetate.
The volatility meta-bolites used water that above-mentioned reduction vaporization operation is evaporated, sulfuric acid or aqueous hydrochloric acid absorb ammonia, to reclaim ammoniacal liquor or preparation ammonium sulfate or ammonium chloride.The ammoniacal liquor that reclaims can return vitamins B
12Or use in other fermentative production, ammonium sulfate or ammonium chloride can be used as fertilizer or other chemical industry raw materials.
The non-volatile acid that above-mentioned acidizing process uses can be mineral acids such as sulfuric acid, phosphoric acid, nitric acid, also can be oxalic acid one class organic acid.When using phosphoric acid, vinasse after the operation underpressure distillation of back can be regulated pH5.0～7.0 with calcium oxide or calcium hydroxide, with pH5.0～6.5 is good, and fully stirring (as stirring 15～30 minutes) after-filtration, drying obtain secondary calcium phosphate, as animal feedstuff additive.Filtrate as discharging of waste liquid or concentrate drying after as feed B
12Weighting agent.When using sulfuric acid, the vinasse after the operation underpressure distillation of back can be regulated pH6.0～8.0 with calcium oxide or calcium hydroxide, be good with pH7.0～7.5, fully stirring (as stirring 15～30 minutes) after-filtration, drying obtain calcium sulfate.
Above-mentioned underpressure distillation operation gained natural polypropylene, acetic acid mixed aqueous solution, can use oxyhydroxide or the oxide compound or the reaction of carbonate reflux of calcium, potassium, sodium, zinc, iron etc., remove by filter insoluble sludge, filtrate decompression has been concentrated into precipitation and has generated, spraying drying or can obtain the saline admixture of natural polypropylene, lime acetate, potassium, sodium, zinc or iron after the additive method drying.Reaction pH control 7.0～9.0 is good with 7.5～8.5; 80 ℃～100 ℃ of temperature of reaction, 2～4 hours reaction times.Why wanting reflux, is for fear of the incomplete free acid volatilization loss of reaction.A small amount of filter residue that filtration obtains can be done the waste residue discharging, or dry back is as feed B
12Weighting agent.For example, in order to obtain the calcium salt admixture of natural polypropylene, acetate, distillation gained natural polypropylene, acetic acid mixed aqueous solution can be regulated pH to 7.0～9.0 with calcium oxide, calcium hydroxide or lime carbonate, 80 ℃～100 ℃ reflux reactions 2～4 hours, continuous as required calcium oxide, calcium hydroxide or the lime carbonate of adding in reaction, keep pH to be not less than 7.5, reaction finishes after-filtration, filtrate decompression has been concentrated into precipitation and has generated, spraying drying or promptly to get the calcium salt admixture of natural polypropylene, acetate after the additive method drying.
The present invention can utilize the bacterium acidi propionici fermented liquid, particularly makes full use of the vitamins B of China's abundant
12Fermentative production waste liquid resource is therefrom extracted natural polypropylene, acetic acid mixed aqueous solution.And can further be processed into their saline admixture such as calcium, sodium, potassium, zinc, iron, byproducts such as also recyclable simultaneously ammonia, ammonium salt, secondary calcium phosphate or calcium sulfate.Its technology is simple, industrialization is easy, the third, the rate of recovery height of acetate, production cost is low, good product quality when turning waste into wealth, can also reduce the quantity discharged of fermented waste fluid and the BOD loading in the waste liquid significantly, alleviate pollution, and be that fermentation productions of ethylformic acid is laid a good foundation with the industrialization that replaces the petrochemical complex propionic acid environment.
Below in conjunction with embodiment and accompanying drawing the present invention is described in detail, but not as a limitation of the invention.
Description of drawings
Accompanying drawing 1 is two step extraction process schemas of the embodiment of the invention.
Accompanying drawing 2 is four step extraction process schemas of the embodiment of the invention.
Accompanying drawing 3 is natural polypropylene, the acetic acid mixed aqueous solution gas chromatogram that extracted in four steps.
Embodiment
Referring to accompanying drawing 1, the first step is regulated pH1.0～5.0 with the bacterium acidi propionici fermented liquid with non-volatile acid, fully stirs (as 15～30 minutes) and makes third in the fermented liquid, acetate be converted into free acid by the form of ammonium salt or other salt; In second step, distilled third, acetic acid mixed aqueous solution are collected in underpressure distillation.Vinasse is regulated pH5.0～7.0 with calcium oxide or calcium hydroxide, filter secondary calcium phosphate or calcium sulfate, filtrate as discharging of waste liquid or concentrate drying after as feed B
12Weighting agent.
Referring to accompanying drawing 2, the first step is regulated pH7.5～10.5 with the bacterium acidi propionici fermented liquid with calcium oxide or calcium hydroxide, fully stirs the back flocculation filtration, after the filter residue and drying as feed or feed B
12Weighting agent; In second step, filtrate is carried out reduction vaporization, and waste gas enters the absorption tower and reclaims ammoniacal liquor or ammonium salt; The 3rd step, reduction vaporization gained concentrated solution is regulated pH1.0～5.0 with non-volatile acid, fully stir (as 15～30 minutes) and make third in the fermented liquid, acetate be converted into free acid by the form of ammonium salt or other salt; The 4th step, underpressure distillation, collect distilled third, acetic acid mixed aqueous solution, vinasse is regulated pH5.0～7.0 (when with the phosphoric acid acidifying) or pH6.0～8.0 (when using sulfuric acid acidation) with calcium oxide or calcium hydroxide, filter secondary calcium phosphate or calcium sulfate, filtrate as discharging of waste liquid or concentrate drying after as feed B
12Weighting agent.
Referring to accompanying drawing 1 and accompanying drawing 2, will by above two kinds of operational paths obtain third, acetic acid mixed aqueous solution regulates about pH8.0 with calcium oxide, calcium hydroxide or lime carbonate (or oxide compound, oxyhydroxide or carbonate of potassium, sodium, zinc, iron), fully stir the back 90～95 ℃ of reflux reactions 2～4 hours, need supplemental calcium, calcium hydroxide or lime carbonate (or oxide compound, oxyhydroxide or carbonate of potassium, sodium, zinc, iron) in case of necessity in the reaction, be not less than 7.0 with the pH that guarantees reaction solution, preferably be not less than 7.5.Reaction finishes after-filtration, can be used as feed B after a small amount of filter residue and drying
12Weighting agent, calcium, potassium, sodium, zinc or molysite mixture that filtrate concentrates, drying can obtain natural polypropylene, acetate.
Specific embodiment 1:
Get bacterium acidi propionici anaerobically fermenting vitamins B
12Produce 3 parts of waste liquids, each 400ml regulates pH3.5 with sulfuric acid, phosphoric acid and oxalic acid respectively, fully stir the back in 80 ℃ of underpressure distillation, collect distillate, with standard NaOH solution titration total acidity, and, the results are shown in table 1 with the content of gas-chromatography separation determination third, acetate.
Table 1 steam after with different sour acidification third, acetic acid mixed aqueous solution relatively
| Fermentating liquid volume (ml) | Acidifying is with sour | Add the acid amount | Acidifying pH | Distillation yield (ml) | Total acidity (mol/L) | Propionic acid content (%w) | Acetic acid content (%w) | Propionic acid yield (%) |
| ????400 | Sulfuric acid | 12ml | ??3.5 | ????106 | ????0.725 | ????4.02 | ????1.09 | ????53.3 |
| ????400 | Phosphoric acid | 20ml | ??3.5 | ????96 | ????0.461 | ????2.81 | ????0.49 | ????33.7 |
| ????400 | Oxalic acid | 3.5g | ??3.5 | ????104 | ????0.590 | ????3.34 | ????0.83 | ????43.4 |
By above result as can be known, the direct acidifying of fermented liquid distill out third, acetate mixed solution acidity and recovery rate be all lower, wherein recovery rate is directly proportional with distillation yield.
Embodiment 2:
Get bacterium acidi propionici anaerobically fermenting vitamins B
12Produce waste liquid 800ml, all be divided into four parts, with Ca (OH)
2Regulate pH8.0 successively, 8.5,9.0 and 9.5, remove by filter precipitation, filtrate is evaporated to only about half of volume respectively at 75～80 ℃, after pH is measured in taking-up, all with sulfuric acid readjustment pH to 2.0, to distillation yield about 60%, the total acidity of measuring distillate is also with the content of gas chromatography determination third, acetate respectively at 70～75 ℃ of underpressure distillation, and result such as table 2 are listed.
PH is to reclaiming the influence of propionic acid concentration and recovery rate for the pre-treatment of table 2 waste liquid alkalescence
| Ferment filtrate (ml) | 200 | ?200 | ?200 | ?200 |
| Ca(OH) 2(g) | 1.08 | ?1.42 | ?1.85 | ?2.28 |
| pH | 8.0 | ?8.5 | ?9.0 | ?9.5 |
| Filter back volume (ml) | 155 | ?150 | ?150 | ?150 |
| 75 ℃ of concentrated volumes (ml) | 80 | ?78 | ?70 | ?85 |
| Concentrate residual volume per-cent (%) | 51.6 | ?52.0 | ?46.7 | ?56.7 |
| Concentrated solution pH | 6.0 | ?6.5 | ?6.5 | ?6.5 |
| 70 ℃ of distillation yields (ml) | 54 | ?44 | ?37 | ?51 |
| Distillation yield per-cent (%) | 67.5 | ?56.4 | ?52.9 | ?60.0 |
| Total acidity (mol/L) | 1.0237 | ?1.1725 | ?1.2146 | ?1.0830 |
| Propionic acid content (g/L) | 50.50 | ?57.84 | ?59.92 | ?53.43 |
| Acetic acid content (g/L) | 20.47 | ?23.45 | ?24.29 | ?21.66 |
| Propionic acid recovery rate (%) | 87.1 | ?83.3 | ?73.3 | ?90 |
By above result as can be known, the total acidity of recovery third, acetate mixture and waste liquid concentrate residual volume per-cent and are inversely proportional to, and recovery rate is directly proportional with distillation yield per-cent, and both all do not have obvious relation with waste liquor PH in 8.0～9.5 scopes.
Embodiment 3:
Get the bacterium acidi propionici ferment filtrate of pH8.5, concentrating under reduced pressure is to about 50% of volume, be divided into 4 parts, every part of 80ml regulates pH3.5 with sulfuric acid respectively, and 3.0,2.5 and 2.0,70 ℃ of underpressure distillation are to distillation yield about 50%, and the total acidity of measuring distillate is also with the content of gas chromatography determination third, acetate, and result such as table 3 are listed.
Table 3 distillation pH is to reclaiming the influence of propionic acid concentration and recovery rate
| Waste liquid concentrated solution volume (ml) | ????80 | ????80 | ????80 | ????80 |
| Add H 2SO 4Amount (ml) | ????3.0 | ????3.5 | ????4.0 | ????4.7 |
| pH | ????3.5 | ????3.0 | ????2.5 | ????2.0 |
| 70 ℃ of distillation yields (ml) | ????38 | ????43 | ????42 | ????40 |
| Distillation yield per-cent (%) | ????47.5 | ????53.75 | ????52.5 | ????50 |
| Total acidity (mol/L) | ????1.1830 | ????1.3514 | ????1.3624 | ????1.5618 |
| Propionic acid content (g/L) | ????58.36 | ????66.67 | ????67.72 | ????77.05 |
| Acetic acid content (g/L) | ????23.66 | ????27.03 | ????27.25 | ????31.24 |
| Propionic acid recovery rate (%) | ????61.6 | ????79.6 | ????78.2 | ????85.5 |
By table 3 data as can be known, reclaim obtain third, the total acidity of acetic acid mixed aqueous solution with distillation before the reduction of acidifying pH rise; Concerning same distillation yield per-cent, the propionic acid rate of recovery also rises with the reduction of acidifying pH before the distillation.
Embodiment 4:
Get the waste liquid 940ml of pH8.5,75 ℃ are evaporated to 145ml, add H
3PO
4Regulate pH2.5, distillation yield 112ml is collected in 70 ℃ of underpressure distillation, surveys total acidity and third, acetic acid content, and calculates the propionic acid recovery rate.Other gets the waste liquid 740ml of pH8.5, and 75 ℃ are evaporated to 150ml, add H
2SO
4Regulate pH2.5, distillation yield 88ml is collected in 70 ℃ of underpressure distillation, surveys total acidity and third, acetic acid content, and calculates the propionic acid recovery rate.Comparative result such as table 4 are listed.
In table 4 phosphoric acid extraction and the sulphuric acid extraction gained overhead product third, the comparison of acetic acid content and propionic acid yield
| Waste liquid volume (ml) | 940 | Waste liquid volume (ml) | 740 |
| pH | ～8.5 | pH | ～8.5 |
| 75 ℃ of concentrated residual volumes (ml) | 145 | 75 ℃ of concentrated residual volumes (ml) | 150 |
| Residual volume per-cent (%) | 15.4 | Residual volume per-cent (%) | 20.3 |
| Add H 3PO 4Amount (ml) | 15 | Add H 2SO 4Amount (ml) | 11.4 |
| pH | ～2.5 | pH | ～2.5 |
| 70 ℃ of distillation yields (ml) | 112 | 70 ℃ of distillation yields (ml) | 88 |
| Distillation yield per-cent (%) | 70.0 | Distillation yield per-cent (%) | 54.5 |
| Total acidity (mol/L) | 3.4322 | Total acidity (mol/L) | 3.3134 |
| Propionic acid content (g/L) | 169.31 | Propionic acid content (g/L) | 163.46 |
| Acetic acid content (g/L) | 68.64 | Acetic acid content (g/L) | 66.27 |
| Propionic acid recovery rate (%) | 93.8 | Propionic acid recovery rate (%) | 90.4 |
| Residual waste solution amount (ml) | 48 | Residual waste solution amount (ml) | 73 |
| Residual waste solution accounts for total waste liquid amount per-cent (%) | 3.5％ | Residual waste solution accounts for total waste liquid amount per-cent (%) | 9.9％ |
Embodiment 5:
In the vinasse of above phosphoric acid acidizing fluid, add Ca (OH)
2, regulate pH6.0, stirred 30 minutes, filter, filter cake gets secondary calcium phosphate 36.2g with no salt solution flushing twice after the drying.
Embodiment 6:
Get the waste liquid 4000ml of pH8.5,80 ℃ are evaporated to 870ml, add vitriol oil 61ml, regulate pH3.5, underpressure distillation is collected distillate once, totally 6 times every about 5 minutes, measure total acidity and third, acetic acid content respectively, and calculate the recovery rate of propionic acid, the results are shown in table 5.
In the distillate of table 5 Fractional Collections third, acetic acid content
Embodiment 7:
| Distillate order | ????1 | ????2 | ????3 | ????4 | ????5 | ???6 | Total or average | |
| Distillation yield (ml) | ????100 | ????100 | ????99 | ????86 | ????78 | ???67 | ????530 | |
| Distillation yield is than (%) | ????10.74 | ????10.74 | ????10.63 | ????9.24 | ????8.38 | ???7.20 | ????56.93 | |
| Acidity (mol/L) | ????2.9440 | ????2.938 | ????3.002 | ????2.94 | ????2.872 | ???2.745 | ????2.917 | |
| Propionic acid | (mol/L) | ????1.9627 | ????1.9587 | ????2.0013 | ????1.9600 | ????1.9147 | ???1.8300 | ????1.945 |
| (g/L) | ????145.39 | ????145.10 | ????148.26 | ????145.19 | ????141.84 | ???135.56 | ????144.074 | |
| Acetate | (mol/L) | ????0.9813 | ????0.9793 | ????1.0007 | ????0.9800 | ????0.9573 | ???0.9150 | ????0.972 |
| (g/L) | ????58.93 | ????58.81 | ????60.09 | ????58.85 | ????57.49 | ???54.95 | ????58.397 | |
| Yield (%) | ????18.17 | ????18.14 | ????18.35 | ????15.61 | ????13.83 | ???11.35 | ????95.45 | |
Get propionic acid content and be 58.23g/L third, acetic acid mixed solution 402ml, add 17.4g Ca (OH)
2, pH value of solution is reached about 8.0, in 90～95 ℃ of reflux 3 hours, be evaporated to driedly, continue to be dried to constant weight, third, lime acetate mixture 39.445g, wherein contain calcium propionate 71.4%, lime acetate 27.9%.Calcium propionate is 96.77% with respect to the molar yield of propionic acid.
Other embodiment (summary).
Referring to accompanying drawing 3, shown is natural polypropylene, acetic acid mixed aqueous solution gas chromatogram, and its chromatographic determination condition is as follows:
1. instrument: gas chromatograph (7890F, sky, Shanghai U.S. company)
2. capillary column: FFAP 0.53 μ m * 0.1 μ m * 30m
3. gas flow rate: carrier gas N
21.4mL/min, combustion gas H
230mL/min, air 400mL/min.
4. detector: hydrogen flame detector
5. service temperature: 145 ℃ of column temperatures, 180 ℃ of sample introduction temperature, 180 ℃ of detected temperatures
6. method of calculation: area normalization method
Sample source: the third, the 39th sample introduction of acetate mixture 02-10-13 08:29
Sample injection time: 2002-10-13 11:16:06 method: system default method (area normalization method)
Packet name retention time peak height peak area area % content % peak, analytical results table peak type
(min)???????(nv)?????(nv
*s)1?????????????0.925????????28???????79????????0.13806????0.13806????BB2?????????????1.311????????2668?????10889?????19.10543???19.10543???BV3?????????????1.501????????8312?????46026?????80.75651???80.75651???VB
From above embodiment as can be known, the propionic acid rate of recovery of four step extraction processes is generally more than 80%, reaches as high as 95%; The third, acetate and its esters purity in mixed aqueous solution or mixing powder all can reach more than 99%; The residual waste solution quantity discharged can reduce to below 10% of former fermented waste fluid volume.Two step extraction processes also can reach basic goal of the invention of the present invention.
Claims (10)
1, a kind of natural polypropylene of bacterium acidi propionici fermented liquid, acetate acidifying distillation and extraction method is characterized in that mainly adopting following processing step:
A, acidifying: promptly regulate fermented liquid pH1.0～5.0, fully stir, make third in the fermented liquid, acetate be converted into free acid by the form of ammonium salt or other salt with non-volatile acid;
B, underpressure distillation: above-mentioned acidifying fermentation liquid is carried out underpressure distillation, and distillate is natural polypropylene, acetic acid mixed aqueous solution.
2, the natural polypropylene of bacterium acidi propionici fermented liquid according to claim 1, acetate acidifying distillation and extraction method is characterized in that the bacterium acidi propionici fermented liquid is bacterium acidi propionici anaerobically fermenting production vitamins B
12Waste liquid behind the separating thallus.
3, the natural polypropylene of bacterium acidi propionici fermented liquid according to claim 1, acetate acidifying distillation and extraction method are regulated pH2.5～3.5 with non-volatile acid when it is characterized in that acidifying.
4, the natural polypropylene of bacterium acidi propionici fermented liquid according to claim 1, acetate acidifying distillation and extraction method, it is characterized in that before acidifying, with calcium oxide or calcium hydroxide fermented liquid being carried out pre-treatment earlier, regulate pH7.0～10.5, fully stir the protein flocculation that makes in the fermented liquid, filtration obtains clear filtrate, to filtrate evaporated under reduced pressure, remove wherein ammonia and other alkalescence and neutral volatility meta-bolites, and make filtrate concentrated then.
5, the natural polypropylene of bacterium acidi propionici fermented liquid according to claim 4, acetate acidifying distillation and extraction method are regulated pH8.0～9.0 with calcium oxide or calcium hydroxide when it is characterized in that the alkali pre-treatment.
6, the natural polypropylene of bacterium acidi propionici fermented liquid according to claim 4, acetate acidifying distillation and extraction method, it is characterized in that volatility meta-bolites water, sulfuric acid or aqueous hydrochloric acid that reduction vaporization is come out absorb ammonia, reclaim ammoniacal liquor or make ammonium sulfate or ammonium chloride.
7, the natural polypropylene of bacterium acidi propionici fermented liquid according to claim 4, acetate acidifying distillation and extraction method, use phosphoric acid when it is characterized in that acidifying, the vinasse that obtains after fermented liquid after the acidifying or the concentrated solution underpressure distillation is regulated pH to 5.0～7.0 with calcium oxide or calcium hydroxide, fully stir after-filtration and obtain secondary calcium phosphate or calcium phosphate.
8, the natural polypropylene of bacterium acidi propionici fermented liquid according to claim 4, acetate acidifying distillation and extraction method, use sulfuric acid when it is characterized in that acidifying, the vinasse that obtains after the concentrated solution underpressure distillation after the acidifying is regulated pH to 6.0～8.0 with calcium oxide or calcium hydroxide, stir after-filtration and obtain calcium sulfate.
9, according to claim 1,2,3,4,5,6,7 or 8 described bacterium acidi propionici fermented liquid natural polypropylenes, acetate acidifying distillation and extraction method, it is characterized in that oxyhydroxide or oxide compound or carbonate neutralization and reacting by heating with above-mentioned distillation gained natural polypropylene, acetic acid mixed aqueous solution calcium, potassium, sodium, zinc, iron, filter, filtrate decompression has been concentrated into precipitation and has generated, spraying drying or with after the additive method drying the mixture of natural polypropylene, lime acetate, potassium, sodium, zinc or molysite.
10, the natural polypropylene of bacterium acidi propionici fermented liquid according to claim 9, acetate acidifying distillation and extraction method, it is characterized in that distillation gained natural polypropylene, acetic acid mixed aqueous solution are regulated pH to 7.0～9.0 with calcium oxide, calcium hydroxide or lime carbonate, 80 ℃～100 ℃ reflux reactions 2～4 hours, continuous as required calcium oxide, calcium hydroxide or the lime carbonate of adding in reaction, keep pH to be not less than 7.5, reaction finishes after-filtration, filtrate decompression has been concentrated into precipitation and has generated, spraying drying or with after the additive method drying the calcium salt admixture of natural polypropylene, acetate.
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103582787A (en) * | 2011-05-18 | 2014-02-12 | 斯科尔生物燃料公司 | Solar-assisted volatile fermentation products production processes |
| CN105026354A (en) * | 2013-03-15 | 2015-11-04 | 陶氏环球技术有限责任公司 | Thermal salt-splitting of ammonium propionate |
| CN111164215A (en) * | 2017-10-02 | 2020-05-15 | 代谢探索者公司 | Method for producing organic acid salts from fermentation broth |
| CN113249412A (en) * | 2021-05-18 | 2021-08-13 | 浙江圣达生物研究院有限公司 | Preparation method of fermentation source calcium propionate |
| CN113373182A (en) * | 2021-06-17 | 2021-09-10 | 四川剑南春（集团）有限责任公司 | Method for recovering caproic acid in biological fermentation liquid |
| CN113481246A (en) * | 2021-06-16 | 2021-10-08 | 浙江圣达生物研究院有限公司 | Method for preparing fermentation source calcium propionate by using ion exchange resin |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB689412A (en) * | 1949-12-17 | 1953-03-25 | Celanese Corp | Fermentation of wood pulp waste liquor to produce aliphatic carboxylic acids |
| US3067107A (en) * | 1959-05-11 | 1962-12-04 | Columbia Cellulose Company Ltd | Propionic acid fermentation |
| UA72220C2 (en) * | 1998-09-08 | 2005-02-15 | Байоенджініерінг Рісорсиз, Інк. | Water-immiscible mixture solvent/cosolvent for extracting acetic acid, a method for producing acetic acid (variants), a method for anaerobic microbial fermentation for obtaining acetic acid (variants), modified solvent and a method for obtaining thereof |
| DE19939630C2 (en) * | 1999-08-20 | 2001-07-12 | Mg Technologies Ag | Process for fine cleaning an aqueous solution containing a fermentatively produced organic acid |
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2003
- 2003-05-15 CN CNB031310656A patent/CN1297529C/en not_active Expired - Fee Related
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103582787A (en) * | 2011-05-18 | 2014-02-12 | 斯科尔生物燃料公司 | Solar-assisted volatile fermentation products production processes |
| CN103582787B (en) * | 2011-05-18 | 2016-09-14 | 斯科尔生物燃料公司 | The production technology of the volatile fermentation products of solar energy auxiliary |
| CN105026354A (en) * | 2013-03-15 | 2015-11-04 | 陶氏环球技术有限责任公司 | Thermal salt-splitting of ammonium propionate |
| CN111164215A (en) * | 2017-10-02 | 2020-05-15 | 代谢探索者公司 | Method for producing organic acid salts from fermentation broth |
| CN113249412A (en) * | 2021-05-18 | 2021-08-13 | 浙江圣达生物研究院有限公司 | Preparation method of fermentation source calcium propionate |
| CN113481246A (en) * | 2021-06-16 | 2021-10-08 | 浙江圣达生物研究院有限公司 | Method for preparing fermentation source calcium propionate by using ion exchange resin |
| CN113373182A (en) * | 2021-06-17 | 2021-09-10 | 四川剑南春（集团）有限责任公司 | Method for recovering caproic acid in biological fermentation liquid |
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| CN1297529C (en) | 2007-01-31 |
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