CN106925595A - A kind of handling process of antibiotic bacterium dregs - Google Patents

A kind of handling process of antibiotic bacterium dregs Download PDF

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Publication number
CN106925595A
CN106925595A CN201511021128.7A CN201511021128A CN106925595A CN 106925595 A CN106925595 A CN 106925595A CN 201511021128 A CN201511021128 A CN 201511021128A CN 106925595 A CN106925595 A CN 106925595A
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China
Prior art keywords
antibiotic bacterium
bacterium dregs
acid
handling process
antibiotic
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CN201511021128.7A
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CN106925595B (en
Inventor
武国庆
张宏嘉
熊强
许克家
林海龙
王骏
郝小明
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Gene Port (hongkong) Biological Technology Co Ltd
Cofco Nutrition and Health Research Institute Co Ltd
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Gene Port (hongkong) Biological Technology Co Ltd
Cofco Nutrition and Health Research Institute Co Ltd
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B09DISPOSAL OF SOLID WASTE; RECLAMATION OF CONTAMINATED SOIL
    • B09BDISPOSAL OF SOLID WASTE NOT OTHERWISE PROVIDED FOR
    • B09B3/00Destroying solid waste or transforming solid waste into something useful or harmless
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B09DISPOSAL OF SOLID WASTE; RECLAMATION OF CONTAMINATED SOIL
    • B09BDISPOSAL OF SOLID WASTE NOT OTHERWISE PROVIDED FOR
    • B09B3/00Destroying solid waste or transforming solid waste into something useful or harmless
    • B09B3/40Destroying solid waste or transforming solid waste into something useful or harmless involving thermal treatment, e.g. evaporation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B09DISPOSAL OF SOLID WASTE; RECLAMATION OF CONTAMINATED SOIL
    • B09BDISPOSAL OF SOLID WASTE NOT OTHERWISE PROVIDED FOR
    • B09B5/00Operations not covered by a single other subclass or by a single other group in this subclass

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  • Engineering & Computer Science (AREA)
  • Environmental & Geological Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Fertilizers (AREA)
  • Processing Of Solid Wastes (AREA)

Abstract

The present invention relates to the process field of organic waste, a kind of handling process of antibiotic bacterium dregs is disclosed, wherein, the handling process includes:In the presence of acidic materials, and in confined conditions, at 40-260 DEG C, pending antibiotic bacterium dregs are degraded, catabolite is then carried out into the gentle phase material stream of isolated solid formation mass flow, and gaseous substance stream is post-processed.By above-mentioned technical proposal, Organic nutrient therein can be effectively retained while the residual antibiotic in effectively degraded antibiotic bacterium dregs, for the innoxious use of bacteria residue provides good precondition.Furthermore, technique of the invention can be prevented effectively from the problem that bacteria residue discharges bad smell in processing procedure and after treatment, and the bacteria residue odorless after treatment is environment-friendly.

Description

A kind of handling process of antibiotic bacterium dregs
Technical field
The present invention relates to a kind of handling process of organic waste, in particular it relates to a kind of antibiotic bacterium dregs Handling process.
Background technology
Antibiotic bacterium dregs are the solid waste of generation during Production by Microorganism Fermentation antibiotic.China It is the first big country of antibiotics production, it is current country's antibiotic that the green of antibiotic bacterium dregs is degraded and utilized A major challenge that manufacturing enterprise faces.
Antibiotic bacterium dregs are main by being blended in microbial cells tissue, culture medium, the production technology of residual Solids phase residue in culture medium, such as filter aid are constituted.The composition of the antibiotic bacterium dregs includes:Source Protein, fat in microorganism and culture medium, carbohydrate, chitin, vitamin, mineral matter And the antibiotic of residual etc..Wherein, the moisture of antibiotic bacterium dregs ordinarily be about 70-95 weight %. The ratio of crude protein is in 30-50 weight % or so in solid waste butt, carbohydrate such as cellulose, The other compositions such as chitin, mineral matter account for the 40-70 weight % of solid waste butt, antibiotic Residual concentration is general between 0.05-6 weight ‰.
At present, antibiotic bacterium dregs are according to hazardous waste disposal.Prior art provides the various ways for utilizing Footpath:As CN104263451A provides a kind of bacteria residue green polymerization fuel and preparation method thereof, the method is proposed Antibiotic bacterium dregs and coal slime and dimerization fuel are prepared as fuel and the scheme burned.
And for example CN104086244A provides the side that a kind of antibiotic bacterium dregs biofermentation converts humus Method, the method carries out solid state fermentation using complex microorganism to material, wherein, the material includes antibiosis Plain bacteria residue and stalk;The complex microorganism includes Trichoderma, bacillus subtilis and bacillus licheniformis, And the Trichoderma, the weight ratio between bacillus subtilis and bacillus licheniformis are (3-5):(2-4):(2-4).The method is used by solid fermentation by using bacteria residue as organic fertilizer raw material.
And for example CN103923599A provides a kind of adhesive prepared based on antibiotic bacterium dregs and bean powder And preparation method thereof, the raw material of the adhesive includes antibiotic bacterium dregs, bean powder and additive.The method What is proposed is by the scheme of the materialized application of antibiotic bacterium dregs.
Although the existing treatment technology of antibiotic bacterium dregs include incineration technology, Fertilizer Transformed technology, landfill and Energy technology etc..However, the treatment of antibiotic bacterium dregs still suffers from lot of challenges.Firstly, for bacterium The antibiotic remained in slag, in addition to burning and carbonization is heat-treated, is difficult to effectively in prior art solutions Degraded, can reenter environment, as the hotbed for cultivating drug-resistant microorganisms.Second, antibiotic bacterium dregs Stacking and processing procedure can discharge bad smell, surrounding environment is polluted so that the mistake for the treatment of Journey faces bigger technical difficulty.
The content of the invention
The purpose of the present invention is to overcome defect of the prior art and provide a kind for the treatment of of antibiotic bacterium dregs Technique, the handling process can effectively reduce the residual concentration of various antibiotic so that at this programme The bacteria residue of reason meets the requirement of innoxious use, and can effectively improve the protein content in bacteria residue.
It was found by the inventors of the present invention that using burning and carbonization heat-treating methods, although can remove anti- Raw element residual, but, the Organic nutrient such as thick protein, amino acid and other organic substances can not Retained.And handling process of the invention can effectively remove residual antibiotic, nutrients can be retained again Matter, that is, eliminate residual antibiotic and remain nutriment again and remove peculiar smell, thus should with good Use prospect.
To achieve these goals, the present invention provides a kind of handling process of antibiotic bacterium dregs, wherein, institute Stating handling process includes:In the presence of acidic materials, and in confined conditions, at 40-260 DEG C, will Pending antibiotic bacterium dregs are degraded, and it is gentle that catabolite then is carried out into isolated solid formation mass flow Phase material stream, and gaseous substance stream is post-processed.
By above-mentioned technical proposal, can be while the residual antibiotic in effectively degraded antibiotic bacterium dregs Organic nutrient therein is effectively retained, for the innoxious use of bacteria residue provides good precondition. Furthermore, technique of the invention can be prevented effectively from bacteria residue release difficult in processing procedure and after treatment The problem of smelling, the bacteria residue odorless after treatment is environment-friendly.
Preferably, after the handling process is additionally included in degraded, it is depressured by the way of steam blasting, is made Front and rear pressure differential at least 0.1MPa, more preferably 0.4-1.2MPa must be depressured.In this process In, cell in bacteria residue can be made fully to crush, rupture, and make wherein each component, such as cellulose and The abundant separate out of nutriment, such as protein, antibiosis is remained so as to be further ensured that in antibiotic bacterium dregs Element is significantly degraded, and is effectively retained nutritional ingredient.
Other features and advantages of the present invention will be described in detail in subsequent specific embodiment part.
Brief description of the drawings
Accompanying drawing is, for providing a further understanding of the present invention, and to constitute the part of specification, with Following specific embodiment is used to explain the present invention together, but is not construed as limiting the invention. In accompanying drawing:
Fig. 1 is a kind of processing technological flow figure of the antibiotic bacterium dregs of specific embodiment of the invention.
Specific embodiment
Specific embodiment of the invention is described in detail below.It should be appreciated that this place is retouched The specific embodiment stated is merely to illustrate and explain the present invention, and is not intended to limit the invention.
According to the present invention, the handling process of the antibiotic bacterium dregs includes:In the presence of acidic materials, And in confined conditions, at 40-260 DEG C, pending antibiotic bacterium dregs are degraded, then will degraded Product carries out the gentle phase material stream of isolated solid formation mass flow, and gaseous substance stream is post-processed. Under preferable case, degradation temperature is more than or equal to 110 DEG C to being less than 200 DEG C, more preferably 120-190℃。
Solid formation mass flow of the present invention refers to solid-liquid of the antibiotic bacterium dregs by generation after degradation treatment Mixture;Described gas gas-phase objects mass flow refers to gas mixing of the antibiotic bacterium dregs by generation after degradation treatment Thing.
Handling process of the invention is used in the presence of acidic materials, and in confined conditions, 40-260 DEG C, pending antibiotic bacterium dregs are degraded, can effectively be reduced antibiotic concentration, improved Solid phase protein content, removes bacteria residue peculiar smell, so as to reach hot acid degraded, harmless treatment and effective profit With triple purposes of material.
According to the present invention, as long as effective degraded of the time guarantee antibiotic of the degraded and organic nutrition Effective preservation of material, under preferable case, the time of the degraded is 0.05-180 minutes, enters one Under step preferable case, when antibiotic bacterium dregs are processed using hot acid method, degradation time can be shorten to 3-80 minutes.
According to the present invention, the pressure of the degraded of the airtight condition can be 3KPa-5MPa, preferably 0.2-1.3MPa。
According to one of the invention preferred embodiment, in order to improve degradation efficiency, it is ensured that antibiotic bacterium The abundant degraded and the retention of nutriment of slag, it is of the invention in the presence of acidic materials, and in closed bar Under part, at 110-260 DEG C, more preferably greater than or equal to 110 DEG C are extremely less than 200 DEG C, further preferably Degraded 0.1-180 minutes for 120-190 DEG C and under 3KPa-5MPa, preferably 0.2-1.3MPa, After preferably 3-80 minutes, i.e. after degrading under these conditions, before catabolite is separated, It is depressured by the way of steam blasting so that the pressure differential before and after step-down is at least 0.1MPa, preferably 0.4-1.2MPa.It is depressured by the way of steam blasting, moment is by the pressure state in closed environment from height Pressure drop is to normal pressure or low pressure, so that the cell in antibiotic bacterium dregs is fully crushed, ruptured;And make wherein Each component, such as cellulosic structure fully opened and nutriment, and such as protein is fully discharged, So that the antibiotic of antibiotic bacterium dregs intraor extracellular is significantly degraded, and further realize hair of the invention Improving eyesight.
According to the present invention, in the presence of acidic materials, and under degradation condition of the present invention, will treat The treatment mode degraded of antibiotic bacterium dregs can be:Before degrading will pending antibiotic bacterium dregs Contacted with acidic materials (for example, mixed pending antibiotic bacterium dregs with acidic materials before charging, Or mix pending antibiotic bacterium dregs with acidic materials in charging), or will in degradation process Pending antibiotic bacterium dregs are contacted with acidic materials, it is also possible to both before degrading by pending antibiotic Bacteria residue is contacted with acidic materials, and again by pending antibiotic bacterium dregs and acidic materials in degradation process Contact.Wherein, described contact is preferably mixing.
According to the present invention, in the presence of acidic materials, pending antibiotic bacterium dregs are degraded, Under identical degradation time, degradation temperature can be reduced, or under identical degradation temperature, drop can be shortened The solution time, while do not interfere with again, or even degradation efficiency can be improved.The present invention is to the acidic materials Species and consumption are not particularly limited, and under preferable case, the consumption of acidic materials causes pending antibiotic Acid concentration is in the range of 0.001M-5M in bacteria residue, preferably 0.005M-1M.
Further preferably, the acidic materials can also be able to be weak acid for strong acid, or strong acid with The combination of weak acid, for example, the strong acid can be selected from the one kind in hydrochloric acid, sulfuric acid, phosphoric acid and pyrophosphoric acid Or it is various, pKa (25 DEG C) value of the weak acid at least above -2, preferably at least above 0;For example, Carboxylic acid can be selected from, such as in fumaric acid, lactic acid, citric acid, formic acid, acetic acid, ethanedioic acid, succinic acid One or more.Additionally, the acidic materials can also be is presented acid amino acid, such as paddy ammonia Acid and/or aspartic acid.
According to the present invention, the method that catabolite is carried out the gentle phase material stream of isolated solid formation mass flow Can be carried out using method well known in the art, for example, by decompression, cooling, such as in cyclone separator In, by the discharge of gaseous matter stream, and isolated solid formation mass flow.Meanwhile, the gaseous substance that will be discharged Stream carries out conventional gas post processing well known in the art, to remove pernicious gas therein.Such as using life The desulfurization of thing method, chemiadsorption etc. are removing the pernicious gases such as ammonia therein, hydrogen sulfide;For another example can be with Using using the tail gas absorption for having peculiar smell or harmful components in the porous medias such as water or activated carbon absorption tail gas Equipment, it would however also be possible to employ for the burning facility of incineration tail gas combustible component, when combustible component contains in tail gas The fuel gas such as biogas, natural gas can be mixed when measuring relatively low carries out mixed burning.
According to the present invention, the water content of the pending antibiotic bacterium dregs can be 20-99 weight %, be Can more efficiently treatment bacteria residue, improve treatment effeciency, it is specific as shown in figure 1, place of the invention Science and engineering skill also includes:Before pending antibiotic bacterium dregs are degraded, will at least part of pending antibiotic Bacteria residue carries out separation of solid and liquid, obtains pending antibiotic bacterium after the dehydration that moisture is 45-90 weight % Slag and liquid phase substance stream, and by pending antibiotic bacterium dregs after dehydration individually degraded or with do not take off The pending antibiotic bacterium dregs of water are degraded together.According to a specific embodiment of the invention, it is Guarantee is effectively contacted with acidic materials, can by pending antibiotic bacterium dregs and acidic materials after dehydration Directly individually degraded after contact, or can also be by pending antibiotic bacterium dregs and selectivity after dehydration Ground contacted with acidic materials be not dehydrated pending antibiotic bacterium dregs together with optionally connect with acidic materials Touch and degraded together.Wherein, " what is optionally contacted with acidic materials is not dehydrated pending antibiosis Plain bacteria residue " and " optionally being contacted with acidic materials together " refer to this without dewater treatment Antibiotic bacterium dregs can first be contacted before degraded with enough acidic materials, directly wait to locate with after dehydration afterwards Managing antibiotic bacterium dregs to be degraded together, or be somebody's turn to do the antibiotic bacterium dregs without dewater treatment to degrade Preceding elder generation contacts with the acidic materials of part, mix with pending antibiotic bacterium dregs after dehydration afterwards and with part Acidic materials are contacted and degraded together, furthermore are somebody's turn to do the antibiotic bacterium dregs without dewater treatment and are treated after being dehydrated Treatment antibiotic bacterium dregs be mixed contacted with acidic materials and together with degraded.
Further preferably, the technique also includes being dehydrated the isolated liquid phase substance stream to moisture containing It is 55-85 weight % to measure, and individually carries out degraded and is preferably returned to together with pending antibiotic bacterium dregs after dehydration Degraded.On the one hand, the dry substance concentration of pending antibiotic bacterium dregs is improved, it is possible to increase equipment Treatment effeciency, is conducive to further reducing the residual concentration of antibiotic, improves solid phase protein content, separately On the one hand, the liquid phase substance stream after separation of solid and liquid is further dehydrated, is such as returned after evaporation, concentration, with Pending antibiotic bacterium dregs are degraded together after dehydration, it is possible to reduce steam consumption, and can be further The a small amount of bacteria residue contained in liquid phase substance stream is carried out into degradation treatment together, treatment effect is improve, and Also it is improved in continuous feed convenience and controllability.
Wherein, the method for the separation of solid and liquid can be used and carried out well known to a person skilled in the art method, It is for instance possible to use the method such as plate-frame filtering.
According to the present invention, in order to further improve degradation effect, the degraded of the pending antibiotic bacterium dregs It is preferred that carrying out under agitation.
According to the present invention, the present invention is preferably in air-liquid two-phase or gas, liquid, solid phase three-phase thermal response mistake Degraded in journey, wherein, there is provided the thermal source of temperature includes steam and/or other heat carriers, mode of heating Can directly be contacted with material and it be conducted heat, or heat carrier is by between container wall for heat carrier Connect and give material heating, or above two mode of heating is combined and carried out.In the preferred case, there is provided temperature Thermal source be steam, the steam can be saturated vapor and/or superheated steam, it is preferable that airtight condition Vapour pressure more than or equal to synthermal lower vapor saturated vapor pressure.
The handling process of antibiotic bacterium dregs of the present invention can be carried out in equipment known in the art, For example, can be in batch (-type) boiling vessel, such as conventional vertical digester, it is also possible in continuous steamer, such as Carried out in conventional transverse tube type continuous steamer or tower continuous steamer.
According to the present invention, the species of the pending antibiotic bacterium dregs is not particularly limited, and can be existing Various antibiotic bacterium dregs in technology, for example, from various following antibiotic bacterium dregs fermentations can be produced to produce Raw bacteria residue and the bacteria residue material comprising the antibiotic, specifically, the antibiotic bacterium dregs can be selected From containing beta-lactam class (such as cynnematin, penicillin), Tetracyclines (such as tetracycline, terramycin), Macrolides (such as erythromycin) class, aminoglycoside (such as gentamicin, streptomysin), polypeptide With the bacteria residue of one or more antibiotic in lincomycin class etc..
In the present invention, institute's finger pressure is absolute pressure.
The preferred embodiment of the present invention described in detail above, but, the present invention is not limited to above-mentioned reality The detail in mode is applied, in range of the technology design of the invention, can be to technical side of the invention Case carries out various simple variants, and these simple variants belong to protection scope of the present invention.
It is further to note that each particular technique feature described in above-mentioned specific embodiment, In the case of reconcilable, can be combined by any suitable means, in order to avoid unnecessary Repeat, the present invention is no longer separately illustrated to various possible combinations.
Additionally, can also be combined between a variety of implementation methods of the invention, as long as its Without prejudice to thought of the invention, it should equally be considered as content disclosed in this invention.
Below will the present invention will be described in detail by embodiment.
In following examples, the pending antibiotic bacterium dregs are the bacteria residue for producing benzyl penicillin and erythromycin; Wherein, the moisture of penicillin mushroom dregs is 81.6 weight %.Butt weight with penicillin mushroom dregs is as base Standard, crude protein content is 40.7 weight %, and fiber content is 6.5 weight %, and crude fat content is 3.5 Weight %, the residual concentration of benzyl penicillin is 2.38 weight ‰ (2380ppm).Wherein, erythromycin bacterium The moisture of slag is 90.1 weight %.On the basis of the butt weight of erythromycin bacterium slag, crude protein content It is 34.1 weight %, fiber content is 2.6 weight %, and crude fat content is 8.9 weight %, erythromycin Residual concentration is 1.71 weight ‰ (1710ppm).
Penicillin/erythromycin is remained in terms of ppm in catabolite in following embodiments and comparative example, 1ppm Equivalent to 0.0001 weight %.
In following examples, the antibiotic crude protein content is determined by the method for kjeldahl determination and obtained, By high performance liquid chromatography tandem mass spectrum method, (liquid chromatogram is Agilent to the content of antibiotic in bacteria residue 7890B, is equipped with binary gradient pump, vacuum on-line degassing machine, automatic sampler;Mass spectrograph is Agilent Company 6540Q-TOF;Instrument controlling, data acquisition software and DAS are public using Agilent The MassHnuter systems of department) method measures.
Chromatographic condition:HSS-T3 chromatographic columns, 100x2.1mm id., 1.8 μm of particle diameter, column temperature:40℃. Mobile phase:A phases are that, containing the aqueous formic acid of 1 mass ‰, B phases are acetonitrile;Flow velocity 0.4ml/min.Sample introduction Volume is 3 μ l.
Mass Spectrometry Conditions:Electron spray positive ion source (ESI+), voltage 3500V dries 300 DEG C of temperature degree, Taper hole voltage 65V, 350 DEG C of sheath temperature degree dries gas and sheath throughput respectively 8L/min and 11L/min, Atomization gas pressure 35psi, full scan pattern (50-1000amu).
In example 1 below -12 and comparative example 1-3, the operating temperature of batch (-type) vertical digester 40-300 DEG C, operating pressure 3KPa-10MPa;In embodiment 13-18 and comparative example 4, continous way 40-210 DEG C of boiling vessel operating temperature, operating pressure 3KPa-1.9MPa.
In following examples, gas processing device be using using activated carbon porous media absorb tail gas in have The tail gas absorption equipment of peculiar smell or harmful components.
Embodiment 1
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
It is 0.01M that pending penicillin mushroom dregs are mixed into regulation to the acid concentration of penicillin mushroom dregs with citric acid, And the penicillin mushroom dregs are placed in batch (-type) vertical digester, it is passed through saturated vapor so that batch (-type) steams Saturated vapor pressure in boiler is 0.2MPa, in airtight condition, at 120 DEG C, under agitation degrade 15 minutes.Batch (-type) boiling vessel is carried out by the quick pressure releasing (pressure before and after pressure release using steam blasting mode Difference is 0.1MPa), discharge gas is separated and sent into by cyclone separator and carry out in gas processing device Post processing, and solid phase catabolite is isolated, measure is obtained, and Penicillin Residues are in catabolite 2.03ppm, crude protein content is 45.8 weight %.
Embodiment 2
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
Method according to embodiment 1 processes penicillin mushroom dregs, unlike, acidic materials are acetic acid, drop Solution temperature is 180 DEG C.Saturated vapor pressure during degraded in boiling vessel is 1.0MPa, the pressure before and after pressure release Difference is 0.9MPa.Measure is obtained, and Penicillin Residues are in catabolite<0.01ppm, crude protein content It is 53.9 weight %.
Embodiment 3
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
Method according to embodiment 1 processes penicillin mushroom dregs, unlike, degradation temperature is 150 DEG C. Saturated vapor pressure during degraded in boiling vessel is 0.476MPa, and the pressure differential before and after pressure release is 0.37MPa. Measure is obtained, and Penicillin Residues are in catabolite<0.01ppm, crude protein content is 51.4 weight %.
Embodiment 4
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
Method according to embodiment 1 processes penicillin mushroom dregs, unlike, acidic materials are acetic acid, drop Solution temperature is 230 DEG C.Saturated vapor pressure during degraded in boiling vessel is 2.8MPa, the pressure before and after pressure release Difference is 2.7MPa.Measure is obtained, and Penicillin Residues are in catabolite<0.01ppm, crude protein content It is 41.7 weight %.
Embodiment 5
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
Method according to embodiment 1 processes penicillin mushroom dregs, unlike, acidic materials are acetic acid, drop Solution temperature is 199 DEG C, and saturated vapor pressure during degraded in boiling vessel is 1.52MPa, the pressure before and after pressure release Power difference is 1.45MPa.Measure is obtained, and Penicillin Residues are in catabolite<0.01ppm, crude protein contains It is 52.1 weight % to measure.
Embodiment 6
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
Method according to embodiment 1 processes penicillin mushroom dregs, unlike, degradation time is 80 minutes. Measure is obtained, and Penicillin Residues are in catabolite<0.01ppm, crude protein content is 49.3 weight %.
Embodiment 7
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
Method according to embodiment 1 processes penicillin mushroom dregs, unlike, degradation time is 45 minutes. Measure is obtained, and Penicillin Residues are 0.02ppm in catabolite, and crude protein content is 47.2 weight %.
Embodiment 8
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
Method according to embodiment 1 processes penicillin mushroom dregs, unlike, used after the completion of degradation reaction The mode of slow step-down carries out pressure release to normal pressure (moment pressure difference is both less than 0.1MPa).Measure is obtained, drop Penicillin Residues are 2.75ppm in solution product, and crude protein content is 44.8 weight %.
Embodiment 9
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
Method according to embodiment 1 processes penicillin mushroom dregs, unlike, institute is mixed with penicillin mushroom dregs Acid is phosphoric acid.Measure is obtained, and Penicillin Residues are in catabolite<0.01ppm, crude protein content It is 47.8 weight %.
Embodiment 10
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
Method according to embodiment 1 processes penicillin mushroom dregs, unlike, tune is mixed with penicillin mushroom dregs The acid concentration for saving penicillin mushroom dregs is 0.82M.Measure is obtained, and Penicillin Residues are in catabolite <0.01ppm, crude protein content is 47.2 weight %.
Embodiment 11
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
Method according to embodiment 1 processes antibiotic bacterium dregs, unlike, handled antibiotic bacterium dregs It is erythromycin bacterium slag.Measure is obtained, and erythromycin residual is 1.02ppm, crude protein content in catabolite It is 36.4 weight %.
Embodiment 12
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
Method according to embodiment 3 processes antibiotic bacterium dregs, unlike, handled antibiotic bacterium dregs It is erythromycin bacterium slag.Measure is obtained, and erythromycin residual is in catabolite<0.01ppm, crude protein content It is 40.8 weight %.
Embodiment 13
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
It is 0.01M that pending penicillin mushroom dregs are mixed into regulation to the acid concentration of penicillin mushroom dregs with citric acid, And the penicillin mushroom dregs are placed in continuous transverse tube boiling vessel, it is passed through saturated vapor so that continuously stewing Saturated vapor pressure in device is 0.2MPa, airtight condition, at 120 DEG C, degrade 15 under agitation Minute.Then, continuous steamer is carried out by the quick pressure releasing (pressure before and after pressure release using steam blasting mode Power difference is 0.1MPa), discharge gas is separated and sent into by cyclone separator and enter in gas processing device Row post processing, and solid phase catabolite is isolated, measure is obtained, and Penicillin Residues are in catabolite 0.59ppm, crude protein content is 46.7 weight %.
Embodiment 14
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
Method according to embodiment 13 processes penicillin mushroom dregs, unlike, degradation temperature is 160 DEG C. Saturated vapor pressure during degraded in boiling vessel is 0.618MPa, and the pressure differential before and after pressure release is 0.517MPa. Measure is obtained, and Penicillin Residues are in catabolite<0.01ppm, crude protein content is 52.5 weight %.
Embodiment 15
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
Method according to embodiment 13 processes penicillin mushroom dregs, unlike, degradation time is 100 points Clock.Measure is obtained, and Penicillin Residues are in catabolite<0.01ppm, crude protein content is 49.8 weights Amount %.
Embodiment 16
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
Method according to embodiment 13 processes penicillin mushroom dregs, unlike, adopted after the completion of degradation reaction Pressure release is carried out with the mode of slow step-down (moment pressure difference is both less than 0.1MPa).Measure is obtained, and degraded is produced Penicillin Residues are 1.21ppm in thing, and crude protein content is 46.0 weight %.
Embodiment 17
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
It is penicillin mushroom dregs described in 81.6 weight % by moisture according to the technological process shown in accompanying drawing 1 Separation of solid and liquid is carried out by plate-frame filtering, solid formation mass flow and liquid phase that water content is 72.5 weight % is obtained Material stream.During the isolated solid formation mass flow sent into continuously stewing device together with citric acid (consumption of acid causes that the acid concentration of penicillin mushroom dregs is maintained at 0.01M), is passed through saturated vapor so that Saturated vapor pressure in continuously stewing device maintains 0.476MPa, airtight condition, at 150 DEG C, Degraded 15 minutes is maintained in continuously stewing device under agitation.Above-mentioned liquid phase substance stream is evaporated, It is concentrated into water content for 72 weight % and this is continuous through pervaporation, the liquid phase substance stream being concentrated to give It is back in continuously stewing device to be degraded together with pending penicillin mushroom dregs after dehydration and (if desired mends Addition acidic materials are filled, then sour consumption causes that the acid concentration of penicillin mushroom dregs remains at 0.01M). After the completion of degraded, continuous steamer is carried out into quick pressure releasing by catabolite using steam blasting mode and (is let out Pressure differential before and after pressure is 0.375MPa) and draw off, discharge gas is separated simultaneously by cyclone separator Post-processed in feeding tail gas treatment device, measure is obtained, and Penicillin Residues are in catabolite <0.01ppm, crude protein content is 51.8 weight %.
Embodiment 18
This example demonstrates that the handling process and its result of the antibiotic bacterium dregs that the present invention is provided.
Method according to embodiment 17 processes antibiotic bacterium dregs, unlike, handled antibiotic bacterium Slag is erythromycin bacterium slag.Measure is obtained, and erythromycin residual is in catabolite<0.01ppm, crude protein contains It is 41.3 weight % to measure.
Comparative example 1
This comparative example is used for the handling process and its result of the antibiotic bacterium dregs for illustrating prior art.
Method according to embodiment 1 processes penicillin mushroom dregs, unlike, it is added without acid, degradation temperature It is 300 DEG C.Measure is obtained, and Penicillin Residues are in catabolite<0.01 weight %, crude protein content is 14.3 weight %.
Comparative example 2
This comparative example is used for the handling process and its result of the antibiotic bacterium dregs for illustrating prior art.
Method according to embodiment 1 processes penicillin mushroom dregs, unlike, it is added without acid, degradation temperature It it is 300 DEG C, degradation time is 120 minutes.Measure is obtained, and Penicillin Residues are in catabolite <0.01ppm, crude protein content is 9.3 weight %.
Comparative example 3
This comparative example is used for the handling process and its result of the antibiotic bacterium dregs for illustrating prior art.
Method according to embodiment 1 processes erythromycin bacterium slag, unlike, degradation temperature is 300 DEG C. Measure is obtained, and erythromycin residual is in catabolite<0.01ppm, crude protein content is 7.5 weight %.
Comparative example 4
This comparative example is used for the handling process and its result of the antibiotic bacterium dregs for illustrating prior art.
Method according to embodiment 13 processes penicillin mushroom dregs, unlike, degradation temperature is 35 DEG C, Degradation time is 120 minutes.Measure is obtained, and Penicillin Residues are 2210ppm, thick egg in catabolite Bai Hanliang is 40.9 weight %.

Claims (14)

1. a kind of handling process of antibiotic bacterium dregs, it is characterised in that the handling process includes: In the presence of acidic materials, and in confined conditions, at 40-260 DEG C, pending antibiotic bacterium dregs are entered Row degraded, then carries out the gentle phase material stream of isolated solid formation mass flow by catabolite, and by gas phase Material stream is post-processed.
2. the handling process of antibiotic bacterium dregs according to claim 1, wherein, the pressure of degraded It is 3KPa-5MPa, preferably 0.2-1.3MPa, the time of degraded is 0.05-180 minutes, preferably 3-80 minutes.
3. the handling process of antibiotic bacterium dregs according to claim 2, wherein, degradation temperature is More than or equal to 110 DEG C to less than 200 DEG C, more preferably 120-190 DEG C.
4. the handling process of antibiotic bacterium dregs according to claim 3, wherein, place's science and engineering Skill also includes:
After degradation, before catabolite is separated, it is depressured by the way of steam blasting so that Pressure differential before and after step-down is at least 0.1MPa, preferably 0.4-1.2MPa.
5. the handling process of the antibiotic bacterium dregs according to any one in claim 1-3, wherein, In the presence of acidic materials, and in confined conditions, at 40-260 DEG C, by pending antibiotic bacterium dregs The method degraded includes:Before pending antibiotic bacterium dregs are degraded, by pending antibiosis Plain bacteria residue is contacted and/or in degradation process with acidic materials, by pending antibiotic bacterium dregs and acidic materials Contact.
6. the handling process of antibiotic bacterium dregs according to claim 5, wherein, acidic materials Acid concentration is 0.001M-5M during consumption makes pending antibiotic bacterium dregs.
7. the handling process of antibiotic bacterium dregs according to claim 6, wherein, acidic materials Acid concentration is 0.005M-1M during consumption makes pending antibiotic bacterium dregs.
8. the handling process of the antibiotic bacterium dregs according to claim 1,6 or 7, wherein, it is described Acidic materials be selected from sulfuric acid, hydrochloric acid, phosphoric acid, pyrophosphoric acid, fumaric acid, lactic acid, citric acid, malic acid, One or more in formic acid, acetic acid, ethanedioic acid, succinic acid and acidic amino acid, it is preferable that the acid Acidic amino acid is glutamic acid and/or aspartic acid.
9. the handling process of antibiotic bacterium dregs according to claim 5, wherein, place's science and engineering Skill also includes:Before pending antibiotic bacterium dregs are degraded, will at least part of pending antibiotic Bacteria residue carries out separation of solid and liquid, obtains pending antibiotic bacterium after the dehydration that moisture is 45-90 weight % Slag and liquid phase substance stream, and pending antibiotic bacterium dregs after dehydration are contacted and dropped with acidic materials Solution, or pending antibiotic bacterium dregs after dehydration are treated with not being dehydrated of optionally being contacted with acidic materials Treatment antibiotic bacterium dregs optionally contact with acidic materials together and together with degraded.
10. the handling process of antibiotic bacterium dregs according to claim 9, wherein, place's science and engineering Skill also includes:It is 55-85 weight % that the isolated liquid phase substance stream is dehydrated to moisture, And return is degraded together with pending antibiotic bacterium dregs after dehydration.
The handling process of 11. antibiotic bacterium dregs according to any one in claim 1-4, wherein, The degraded is carried out under agitation.
The handling process of 12. antibiotic bacterium dregs according to claim 1 or 3, wherein, there is provided drop Solve temperature thermal source be saturated vapor and/or superheated steam, and cause airtight condition vapour pressure be more than or Equal to the saturated vapor pressure of synthermal lower vapor.
Place's science and engineering of 13. antibiotic bacterium dregs according to any one in claim 1-4,9 and 10 Skill, wherein, the water content of the pending antibiotic bacterium dregs is 20-99 weight %.
Place's science and engineering of 14. antibiotic bacterium dregs according to any one in claim 1-4,9 and 10 Skill, wherein, antibiotic bacterium dregs are selected from and contain beta-lactam class, Tetracyclines, macrolides, amino One or more bacteria residue in glucosides, polypeptide and lincomycin series antibiotics.
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CN109013641A (en) * 2018-07-11 2018-12-18 清华大学 A kind of method of antibiotic bacterium dregs removing toxic substances
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