CN205368356U - Microbial inoculant production line - Google Patents
Microbial inoculant production line Download PDFInfo
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- CN205368356U CN205368356U CN201521063845.1U CN201521063845U CN205368356U CN 205368356 U CN205368356 U CN 205368356U CN 201521063845 U CN201521063845 U CN 201521063845U CN 205368356 U CN205368356 U CN 205368356U
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Abstract
The utility model relates to a microbial fermentation production field especially relates to a microbial inoculant production line, and this production line is processing system before the material that connects gradually, fermentation workshop and drying plant, processing system is including mixer, the lifting machine that connects gradually, the fungi tank that goes out, cooling fluidized bed and solid -state inoculation device before the material, the fermentation workshop is including the fermented storehouse and the after -ripening storehouse that connect gradually, the drying plant is including the fluidizing drying bed, rubbing crusher, mixed machine and the packagine machine that connect gradually, wherein, solid -state inoculation device is equipped with the device that opens and shuts, the feed inlet in fermentation storehouse corresponds the device setting of opening and shutting of solid -state inoculation device, the after -ripening storehouse is passed through the third material and is carried the auger to connect fluidizing drying bed feed inlet. The utility model discloses all automize all processes, greatly reduced labor operational intensity and time, has improved production efficiency, but also has produced each link and control more easily, guarantee product quality's the dough stability.
Description
Technical field
This utility model relates to fermentable production field, particularly relates to a kind of microbial bacterial agent production line.
Background technology
Owing to microbial bacterial agent is significantly high to the requirement of production environment, traditional handicraft is all in clean room, cultivates through incubator, has entirely manually operated production, is difficult to large-scale production, it is achieved industrialization.
Utility model content
For the technical problem existed in background technology, a kind of microbial bacterial agent production line of the purpose of this utility model offer, utilize full-automatic plant equipment to carry out organic waste converting production, finally obtain microbial bacterial agent.
The technical solution of the utility model is achieved in that
A kind of microbial bacterial agent production line, including the material preprocessing system being sequentially connected with, fermentation plant and drying plant；Described material preprocessing system includes the blender, elevator, sterilization tank, cooling bed and the solid-state classification inoculation apparatus that are sequentially connected with；Described fermentation plant includes the fermentation cabin and the after-ripening storehouse that are sequentially connected with；Described drying plant includes the boiling-bed drying, pulverizer, mixer and the packer that are sequentially connected with；Wherein, described solid-state classification inoculation apparatus is provided with closing device, and the closing device of the corresponding described solid-state classification inoculation apparatus of the charging aperture of described fermentation cabin is arranged；Described after-ripening storehouse connects boiling-bed drying charging aperture by 3 material conveying auger.
Preferably, described blender connects the feeding port of described elevator, the feed opening of described elevator waves conveying auger by first and connects sterilization tank charging aperture, being correspondingly provided with the charging aperture of vibrations blanking device below sterilization tank discharging opening, the discharging opening of described vibrations blanking device is connected on the upside of the left end of described cooling bed；Described solid-state classification inoculation apparatus it is provided with on the downside of the right-hand member of described cooling bed.
Preferably, described fermentation cabin is provided with fermentation cabin discharging opening, and described fermentation cabin discharging opening connects after-ripening storehouse charging aperture by the second material conveyor.
Preferably, described boiling-bed drying connects pulverizer by the first conveyer belt, and described pulverizer connects mixer by the second conveyer belt；Described mixer connects packer by the 3rd conveyer belt.
Preferably, the left end side of described boiling-bed drying is provided with boiling-bed drying charging aperture；Top is provided with exhaustor；Lower end is provided with air inlet pipe and boiling-bed drying discharging opening；Inside is provided with cleaner unit and fabric swatch.
Preferably, described batch mixer left end side is provided with reductor, and upper end is provided with charge door and Butterworth Hatch, and lower end is provided with batch mixer discharging opening.
This utility model is compared with prior art, there is advantages below: this utility model, by all of operation all automatizatioies, greatly reduces manual operation intensity and time, realizes dispensing either directly through mechanization, charging, inoculation, fermentation, dry, packing, improve production efficiency, and produce each link and be easier to control, it is ensured that the stability of product quality.
Accompanying drawing explanation
Fig. 1 is structural representation of the present utility model；
Fig. 2 is the structural representation of this utility model material preprocessing system；
Fig. 3 is the structural representation of this utility model solid-state classification inoculation apparatus；
Fig. 4 is the structural representation of this utility model fermentation plant；
Fig. 5 is the structural representation of this utility model drying plant.
In figure: 1-material preprocessing system；2-fermentation plant；3-drying plant；4-blender；5-elevator；6-sterilization tank；7-cooling bed；8-fermentation cabin；9-the second material conveyor；10-after-ripening storehouse；11-3 material conveying auger；12-boiling-bed drying；13-pulverizer；14-mixer；15-packer；16-solid-state classification inoculation apparatus；17-sieve plate；18-first waves conveying auger；19-shakes blanking device；20-sterilization tank discharging opening；21-closing device；22-fermentation cabin discharging opening；23-after-ripening storehouse charging aperture；24-the first conveyer belt；25-the second conveyer belt；26-the 3rd conveyer belt；27-boiling-bed drying charging aperture, 28-exhaustor, 29-cleaner unit；30-fabric swatch；31-air inlet pipe；32-boiling-bed drying discharging opening；33-charge door；34-Butterworth Hatch；36-batch mixer discharging opening；37-sterilization tank charging aperture；38-fermentation cabin charging aperture；39-after-ripening bin discharge port external.
Detailed description of the invention
Below in conjunction with accompanying drawing, the utility model is described in further detail, but is not intended as the foundation to this utility model restriction.
Refer to Fig. 1～5, a kind of microbial bacterial agent production line described in the utility model includes the material preprocessing system 1 being sequentially connected with, fermentation plant 2 and drying plant 3.
Refer to Fig. 2, for the structural representation of this utility model material preprocessing system.Described material preprocessing system 1 includes blender 4, elevator 5, sterilization tank 6, cooling bed 7 and solid-state classification inoculation apparatus 16, described blender 4 connects the feeding port of described elevator 5, the feed opening of described elevator 5 waves conveying auger 18 by first and connects sterilization tank charging aperture 37, being correspondingly provided with the charging aperture of vibrations blanking device 19 below sterilization tank discharging opening 20, the discharging opening of described vibrations blanking device 19 is connected on the upside of the left end of described cooling bed 7；It is provided with solid-state classification inoculation apparatus 16 on the downside of the right-hand member of described cooling bed 7.Refer to Fig. 3, for the structural representation of this utility model solid-state classification inoculation apparatus.Described solid-state classification inoculation apparatus 16 includes removable lid 161, hopper 162, motor 163, rotates Quantitative dosing valve 164 and discharging opening 165；Described hopper 162 top movable connects removable lid 161, is discharging opening 165 below described hopper 162, and described discharging opening 165 is directly engaged on the discharging opening of described cooling bed 7, has quantitative effect；Described rotation Quantitative dosing valve 164 is connected on described hopper 162；Described rotation Quantitative dosing valve 164 1 side shaft connects motor 163.
The material of described blender 4 stirring is transported to described sterilization tank charging aperture 37 by elevator 5, material is transported to described cooling bed 7 in described sterilization tank 6 after sterilizing, inoculate again through described solid-state classification inoculation apparatus 16 after described cooling bed 7 is lowered the temperature, finally enter fermentation plant 2 by automatic open/closing device 21.
Refer to the structural representation that Fig. 1 and Fig. 4, Fig. 4 are this utility model fermentation plant.Described fermentation plant 2 includes the fermentation cabin 8 and the after-ripening storehouse 10 that are sequentially connected with, the closing device 21 of the corresponding described solid-state classification inoculation apparatus 16 of fermentation cabin charging aperture 38 is arranged, fermentation cabin discharging opening 22 connects after-ripening storehouse charging aperture 23 by the second material conveyor 9, and after-ripening bin discharge port external 39 enters drying plant 3 by 3 material conveying auger 11.Being provided with sieve plate 17 bottom described fermentation cabin 8, it is 40 °-45 ° that described sieve plate 37 is provided with the angle in multiple air-vent (not shown), described air-vent and sieve plate plate face.
Material through the inoculation of described solid-state classification inoculation apparatus 16 is entered fermentation cabin 8 by described fermentation cabin charging aperture 38 and ferments, sieve plate 17 bottom described fermentation cabin 8 can be that fermentation cabin 8 is ventilated by passage, it is delivered to after-ripening storehouse 10 by the second material conveyor 9 after material fermentation, is finally entered drying plant 3 from after-ripening bin discharge port external 39 by 3 material conveying auger 11.
Refer to the structural representation that Fig. 1 and Fig. 5, Fig. 5 are this utility model drying plant 3.Described drying plant 3 includes the boiling-bed drying 12, pulverizer 13, mixer 14 and the packer 15 that are sequentially connected with, and described boiling-bed drying 12 connects pulverizer 13 by the first conveyer belt 24, and described pulverizer 13 connects mixer 14 by the second conveyer belt 25；Described mixer 14 connects packer 15 by the 3rd conveyer belt 26.Described boiling-bed drying 12 left end side is provided with boiling-bed drying charging aperture 27, and top is provided with exhaustor 28, and lower end is provided with air inlet pipe 31 and boiling-bed drying discharging opening 32；Inside is provided with cleaner unit 29 and fabric swatch 30.Described batch mixer 14 left end side is provided with reductor 35, and upper end is provided with charge door 33 and Butterworth Hatch 34, and lower end is provided with batch mixer discharging opening 36.
It is dried that the microbial inoculum fermented enters boiling-bed drying 12 by 3 material conveying auger 11, enter pulverizer 13 by the first conveyer belt 24 to pulverize, after the second conveyer belt 25 enters mixer 14, enter packer 15 then through the 3rd conveyer belt 26, packer 15 be packaged into product.
Advantage of the present utility model:
1, this utility model reduces hand labor intensity by automatic production line
2, this utility model integration of equipments degree is high, decreases in manual operation in the processes such as product turnover, preservation environment to product impact.
This production line can fundamentally change scientific research and disconnect with producing；Transformation of scientific findings rate is low；Lot of research only rests on the present situations such as laboratory stage, it is achieved the slitless connection of scientific research and production.
Obviously, this utility model can be carried out various change and modification without deviating from spirit and scope of the present utility model by those skilled in the art.So, if these amendments of the present utility model and modification belong within the scope of this utility model claim and equivalent technologies thereof, then this utility model is also intended to comprise these change and modification.
Claims (6)
1. a microbial bacterial agent production line, it is characterised in that: include the material preprocessing system being sequentially connected with, fermentation plant and drying plant；Described material preprocessing system includes the blender, elevator, sterilization tank, cooling bed and the solid-state classification inoculation apparatus that are sequentially connected with；Described fermentation plant includes the fermentation cabin and the after-ripening storehouse that are sequentially connected with；Described drying plant includes the boiling-bed drying, pulverizer, mixer and the packer that are sequentially connected with；Wherein, described solid-state classification inoculation apparatus is provided with closing device, and the closing device of the corresponding described solid-state classification inoculation apparatus of the charging aperture of described fermentation cabin is arranged；Described after-ripening storehouse connects boiling-bed drying charging aperture by 3 material conveying auger.
2. microbial bacterial agent production line according to claim 1, it is characterized in that: described blender connects the feeding port of described elevator, the feed opening of described elevator waves conveying auger by first and connects sterilization tank charging aperture, being correspondingly provided with the charging aperture of vibrations blanking device below sterilization tank discharging opening, the discharging opening of described vibrations blanking device is connected on the upside of the left end of described cooling bed；Described solid-state classification inoculation apparatus it is provided with on the downside of the right-hand member of described cooling bed.
3. microbial bacterial agent production line according to claim 1, it is characterised in that: described fermentation cabin is provided with fermentation cabin discharging opening, and described fermentation cabin discharging opening connects after-ripening storehouse charging aperture by the second material conveyor.
4. microbial bacterial agent production line according to claim 1, it is characterised in that: described boiling-bed drying connects pulverizer by the first conveyer belt, and described pulverizer connects mixer by the second conveyer belt；Described mixer connects packer by the 3rd conveyer belt.
5. microbial bacterial agent production line according to claim 1, it is characterised in that: the left end side of described boiling-bed drying is provided with boiling-bed drying charging aperture；Top is provided with exhaustor；Lower end is provided with air inlet pipe and boiling-bed drying discharging opening；Inside is provided with cleaner unit and fabric swatch.
6. microbial bacterial agent production line according to claim 1, it is characterised in that: described mixer left end side is provided with reductor, and upper end is provided with charge door and Butterworth Hatch, and lower end is provided with mixer discharging opening.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201521063845.1U CN205368356U (en) | 2015-12-18 | 2015-12-18 | Microbial inoculant production line |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201521063845.1U CN205368356U (en) | 2015-12-18 | 2015-12-18 | Microbial inoculant production line |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN205368356U true CN205368356U (en) | 2016-07-06 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201521063845.1U Expired - Fee Related CN205368356U (en) | 2015-12-18 | 2015-12-18 | Microbial inoculant production line |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN205368356U (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105349408A (en) * | 2015-12-18 | 2016-02-24 | 陕西博秦生物工程有限公司 | Microbial agent production line |
| CN106694469A (en) * | 2017-02-04 | 2017-05-24 | 青岛金典生化器材有限公司 | Bacterial culture dish production line with culture medium contained inside |
-
2015
- 2015-12-18 CN CN201521063845.1U patent/CN205368356U/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105349408A (en) * | 2015-12-18 | 2016-02-24 | 陕西博秦生物工程有限公司 | Microbial agent production line |
| CN106694469A (en) * | 2017-02-04 | 2017-05-24 | 青岛金典生化器材有限公司 | Bacterial culture dish production line with culture medium contained inside |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20160706 Termination date: 20161218 |
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| CF01 | Termination of patent right due to non-payment of annual fee |