CN120815199A - A rapid sterilization device and method for bovine collagen peptide - Google Patents

Abstract

The present invention relates to the field of sterilization technology, and discloses a bovine collagen peptide rapid sterilization device and sterilization method, comprising two annular frames and a rotating rod coaxially arranged with the annular frames, the two annular frames being coaxially arranged up and down, a plurality of reaction cylinders being coaxially arranged within the annular frames, the reaction cylinders being rotated on the inner walls of the annular frames via support frames, and the reaction cylinders being provided with a bovine collagen peptide input pipe and a carbon dioxide input pipe for passing bovine collagen peptide and carbon dioxide into a mixing cylinder. The electronic control system of the present invention turns off the second electromagnetic generator, so that the end cover no longer blocks the mixing cylinder. At this time, the high-pressure compression chamber is rapidly released, releasing the bovine collagen peptide and carbon dioxide mixture in the compression chamber. The carbon dioxide dissolves in water under high pressure to generate carbonic acid, lowering the pH value, and then penetrates into microbial cells and rapidly reduces pressure, causing the cells to rupture and produce an explosive effect, thereby killing bacteria, yeast, and mold.

Description

Bovine bone collagen peptide rapid sterilization device and sterilization method

Technical Field

The invention relates to the technical field of sterilization, in particular to a bovine bone collagen peptide rapid sterilization device and a sterilization method.

Background

Bovine collagen peptide is sensitive to heat, and conventional heat sterilization methods (such as high temperature instantaneous sterilization) are easy to cause denaturation and inactivation, generate Maillard reaction and have bad flavor, so that the whole process needs to be carried out at low temperature or instantaneous middle temperature, usually less than 65 ℃ to prevent collagen peptide denaturation, and therefore conventional heat sterilization methods are not suitable for bovine collagen peptide sterilization, and therefore, non-heat sterilization methods are usually adopted for bovine collagen peptide sterilization, but the following problems exist in the sterilization methods:

Firstly, because the deactivation phenomenon of bovine bone collagen peptide caused by high temperature is avoided, an ultraviolet lamp is adopted to kill microorganism cells in the bovine bone collagen peptide, and secondly, the direct ultraviolet sterilization is not usually realized to fully cover the bovine bone collagen peptide, so that the sterilization is required to be continuously stirred in the area which is not irradiated by ultraviolet rays, and the sterilization efficiency is definitely reduced.

Therefore, we design a bovine bone collagen peptide rapid sterilization device and a sterilization method.

Disclosure of Invention

The invention aims to solve the problem of inactivation of bovine collagen peptide caused by high temperature in the prior art, and provides a rapid sterilization device and a rapid sterilization method for bovine collagen peptide.

In order to achieve the above purpose, the present invention adopts the following technical scheme:

The quick sterilizing device for bovine bone collagen peptide comprises two annular frames and a rotating rod coaxially arranged with the annular frames, wherein the two annular frames are coaxially arranged up and down, a plurality of reaction cylinders are coaxially arranged in the annular frames, the reaction cylinders are circumferentially arranged, the reaction cylinders rotate on the inner wall of the annular frames through supporting frames, a bovine bone collagen peptide input pipe and a carbon dioxide input pipe for leading bovine bone collagen peptide and carbon dioxide into the mixing cylinders are arranged on the reaction cylinders, a plurality of mixing cylinders are arranged in the reaction cylinders, and the mixing cylinders are linearly fixed in the reaction cylinders through cylinder supports;

The rotating rod is provided with a plurality of rotating shafts which are coaxially inserted into the reaction cylinder, the rotating shafts are inserted into the mixing cylinder, the piston is arranged in the mixing cylinder in a sliding mode, the mixing cylinder is divided into a compression cavity and an stirring cavity, the outer side wall of the rotating shaft is provided with a spiral body positioned in the stirring cavity, the spiral body drives the piston to extrude the bovine bone collagen peptide and carbon dioxide mixture positioned in the compression cavity, and one end of the mixing cylinder is provided with an end cover which is movably arranged and discharges the bovine bone collagen peptide.

Preferably, a plurality of driving mechanisms are arranged on the rotating rod along the shaft, each driving mechanism comprises a plurality of driving motors, the driving motors correspond to the reaction cylinders one by one, and the output ends of the driving motors are coaxially fixed with the rotating shaft.

Preferably, the inner wall of the mixing cylinder is fixed with a limiting frame, a rectangular rigid inserted rod sliding on the limiting frame is fixed on the piston, the rectangular rigid inserted rod is propped against the spiral body, the rotation direction of the spiral body faces the piston, and the piston is connected with the end cover through a first reset spring.

Preferably, the end cover coaxially slides at the end part of the mixing cylinder through the sliding groove and the limiting inserted bar, the sliding groove is formed in the end part of the mixing cylinder, the second electromagnetic generator is arranged in the sliding groove, the limiting inserted bar is reset and stretches in the sliding groove through the second reset spring, and the limiting inserted bar is provided with a first magnet plate towards one side of the second electromagnetic generator.

Preferably, the inner wall of the mixing cylinder is provided with a first material-thinning hole and a second material-thinning hole which are mutually communicated, the first material-thinning hole and the second material-thinning hole are positioned on two sides of the piston, and an electromagnetic pump is arranged in the first material-thinning hole.

Preferably, the mixing drum is coaxially fixed with a stable ventilation disc, the stable ventilation disc is inserted with a second communicating pipe, a vent hole communicated with the stirring cavity is formed in the rotating shaft, and the stable ventilation disc is communicated with the vent hole through an air inlet hole.

Preferably, the mixing drum lateral wall is provided with the buffer tank, and the buffer tank passes through the intercommunicating pore and mixing drum intercommunication, and the buffer tank is the elastic tank, and the mixing drum lateral wall slides there is the baffle ring that is used for blocking the intercommunicating pore, still is fixed with first electromagnetic generator in the buffer tank, and the baffle ring slides through the gag lever post of fixing on first electromagnetic generator, and gag lever post sliding end is equipped with the tip magnetic path, and the baffle ring is equipped with the second magnet board towards first electromagnetic generator one side, is provided with first connecting pipe on the buffer tank.

Preferably, the bovine bone collagen peptide input pipe is communicated with the first communicating pipe through a rubber hose, the carbon dioxide input pipe is communicated with the second communicating pipe through a rubber hose, the bovine bone collagen peptide discharge pipe is arranged at the bottom of the reaction cylinder, and the carbon dioxide discharge pipe is arranged at the top of the side wall of the reaction cylinder.

Preferably, the spiral body is fixed with the tip board that offsets with mixing drum tip inner wall towards firm vent disc one side, and mixing drum tip inner wall is provided with the trigger portion, and the trigger portion is including first flexible point and the flexible point of second that triggers, and the fillet has all been seted up to first flexible point and the flexible point tip that triggers of second, and the trigger portion passes through electrical system and links to each other with first electromagnetic generator, second electromagnetic generator and electromagnetic pump.

A sterilization method of a bovine bone collagen peptide rapid sterilization device comprises the following specific operation steps:

firstly, pumping bovine bone collagen peptide into a buffer box through a bovine bone collagen peptide input pipe and a rubber hose, then enabling the bovine bone collagen peptide to enter a mixing cylinder through a communication hole, and pumping carbon dioxide into a stable ventilation disc through a carbon dioxide input pipe and the rubber hose to finish the effect of introducing the bovine bone collagen peptide and the carbon dioxide into the mixing cylinder;

S2, driving the rotating rod to rotate, wherein the rotating rod can drive the reaction cylinder to rotate on the inner wall of the annular frame through the support frame when rotating, and meanwhile, a driving motor arranged in the driving mechanism drives the rotating rod to rotate, and the rotating force is transmitted into a mixing cylinder positioned in the reaction cylinder;

s3, rotating the rotating shaft with the screw body to rotate together, primarily mixing and stirring the bovine collagen peptide and the carbon dioxide, and extruding and compressing the mixture of the bovine collagen peptide and the carbon dioxide in the cavity by the piston to dissolve the carbon dioxide in water under high pressure so as to realize carbonic acid dissolution and pH value reduction;

s4, protruding a first trigger expansion point through an electric control system, enabling the screw body carrying the end plate to pass through a second trigger expansion point which is not protruding at the moment, pressing and retracting the screw body against the first trigger expansion point, protruding the second trigger expansion point at the moment, and enabling the piston to compress the compression cavity to a state that compression cannot be continued;

S5, the electric control system turns off the second electromagnetic generator, releases the mixture of bovine collagen peptide and carbon dioxide in the compression cavity, and rapidly decompresses after penetrating into microbial cells, so that the cells are broken to generate a blasting effect, and bacteria, yeast and mould are killed;

S6, starting an electromagnetic pump to enable the first material-thinning holes to be communicated with the second material-thinning holes, and extruding the mixture of bovine bone collagen peptide and carbon dioxide which originally exist in the stirring cavity into the compression cavity through the first material-thinning holes and the second material-thinning holes;

And S7, then, the second triggering telescopic point is pressed for retraction, and then, an external pump is started, so that bovine bone collagen peptide is fed through the bovine bone collagen peptide input pipe and carbon dioxide through the carbon dioxide input pipe, the bovine bone collagen peptide after sterilization is discharged from the bovine bone collagen peptide discharge pipe, and carbon dioxide is discharged from the carbon dioxide discharge pipe at the top of the side wall of the reaction cylinder.

The beneficial effects of the invention are as follows:

1. according to the invention, the screw body continuously rotates, the rectangular rigid inserted rod can be separated from the end part of the screw body, the piston moves reversely under the action of the first reset spring, the compression cavity is not compressed, and then the rectangular rigid inserted rod is propped against the outer side wall of the screw body again, namely, the stirring cavity can be continuously mixed with the bovine bone collagen peptide and the carbon dioxide along with the rotation of the rotating shaft with the screw body, and the continuous pressurization and pressure release of the mixture of the bovine bone collagen peptide and the carbon dioxide in the compression cavity can be realized.

2. The electronic control system of the invention closes the second electromagnetic generator to ensure that the end cover does not block the mixing drum, the compression cavity at high pressure can be released rapidly at the moment, the mixture of bovine collagen peptide and carbon dioxide in the compression cavity is released, the carbon dioxide is dissolved in water under high pressure to form carbonic acid, the pH value is reduced, and then the solution is quickly decompressed after penetrating into microbial cells, so that the cells are broken to generate a blasting effect, thereby killing bacteria, yeasts and moulds.

Drawings

Fig. 1 is a schematic structural diagram of a bovine collagen peptide rapid sterilization device according to the present invention;

Fig. 2 is a schematic structural diagram of a reaction cylinder in a bovine bone collagen peptide rapid sterilization device according to the present invention;

Fig. 3 is a main sectional view of a reaction cylinder in the bovine bone collagen peptide rapid sterilization device according to the present invention;

fig. 4 is a schematic structural diagram of a mixing drum in a bovine bone collagen peptide rapid sterilization device according to a first embodiment of the present invention;

FIG. 5 is an enlarged schematic view of the structure shown at A in FIG. 4;

Fig. 6 is a left and right isometric view of a mixing drum in the bovine bone collagen peptide rapid sterilization device according to the present invention;

Fig. 7 is a main sectional view showing a first state of a mixing drum in a bovine bone collagen peptide rapid sterilization apparatus according to the present invention;

FIG. 8 is an enlarged schematic view of the structure at B in FIG. 7;

fig. 9 is a schematic structural diagram of a screw in a bovine collagen peptide rapid sterilization device according to the present invention;

Fig. 10 is a schematic diagram showing a second state structure of a mixing drum in the bovine collagen peptide rapid sterilization device according to the present invention;

fig. 11 is a main sectional view showing a second state of a mixing drum in a bovine bone collagen peptide rapid sterilization apparatus according to the present invention;

fig. 12 is a schematic structural diagram of a trigger part in the bovine collagen peptide rapid sterilization device according to the present invention.

1, An annular frame, 2, a reaction cylinder, 3, a support frame, 4, a rotating rod, 5, a rotating shaft, 6, a bovine bone collagen peptide input pipe, 7, a carbon dioxide input pipe, 8, a carbon dioxide discharge pipe, 9, a bovine bone collagen peptide discharge pipe, 10, a driving mechanism, 11, a mixing cylinder, 12, an end cover, 13, a buffer box, 14, a screw, 15, an end plate, 16, a vent hole, 17, an air inlet, 18, a piston, 19, a first return spring, 20, a compression cavity, 21, an agitating cavity, 22, a first communication pipe, 23, a stable vent disc, 24, a second communication pipe, 25, a communication hole, 26, a baffle ring, 27, a first electromagnetic generator, 28, a limit rod, 29, an end magnet, 30, a first material-thinning hole, 31, a second material-thinning hole, 32, a limit frame, 33, a rectangular rigid insert rod, 34, a limit insert rod, 35, a sliding groove, 36, a second electromagnetic generator, 37 and a second return spring;

38. trigger part 381, first trigger expansion point 382, second trigger expansion point.

Detailed Description

Referring to fig. 1-12, a bovine bone collagen peptide rapid sterilization device comprises two annular frames 1 and a rotating rod 4 coaxially arranged with the annular frames 1, wherein the two annular frames 1 are coaxially arranged up and down, a plurality of reaction cylinders 2 are coaxially arranged in the annular frames 1, the plurality of reaction cylinders 2 are circumferentially arranged, and the reaction cylinders 2 rotate on the inner wall of the annular frames 1 through a supporting frame 3 to provide driving force for the rotation of the reaction cylinders 2.

The reaction cylinder 2 is provided with a bovine bone collagen peptide input pipe 6 and a carbon dioxide input pipe 7 which are used for leading bovine bone collagen peptide and carbon dioxide into a mixing cylinder 11, the reaction cylinder 2 is internally provided with a plurality of mixing cylinders 11, and the mixing cylinders 11 are linearly fixed in the reaction cylinder 2 through a cylinder bracket.

Let bovine bone collagen peptide pump into buffer 13 through bovine bone collagen peptide input tube 6 and rubber hose, then this part bovine bone collagen peptide enters into mixing drum 11 through intercommunicating pore 25, coaxial firm vent disc 23 of being fixed with on the mixing drum 11, and firm vent disc 23 is last to be inserted and be equipped with second communicating pipe 24, bovine bone collagen peptide input tube 6 passes through rubber hose and first communicating pipe 22 intercommunication, carbon dioxide input tube 7 passes through rubber hose and communicates with second communicating pipe 24, set up the air vent 16 with stirring chamber 21 intercommunication on the axis of rotation 5, firm vent disc 23 passes through inlet port 17 and air vent 16 intercommunication, and carbon dioxide then is through carbon dioxide input tube 7 and rubber hose pump firm vent disc 23, then the carbon dioxide that is located firm vent disc 23 enters into air vent 16 through inlet port 17 on axis of rotation 5, then reach in the mixing drum 11, consequently, accomplish the effect to leading in bovine bone collagen peptide and carbon dioxide in the mixing drum 11.

The upper edge axle of dwang 4 is provided with a plurality of actuating mechanism 10, and actuating mechanism 10 includes a plurality of driving motor, and driving motor and reaction section of thick bamboo 2 one-to-one, and driving motor's output is coaxial fixedly with axis of rotation 5, through opening peripheral hardware actuating mechanism, drives dwang 4 and rotates, because actuating mechanism 10 that sets up on the dwang 4 to and actuating mechanism 10 link to each other with reaction section of thick bamboo 2 through axis of rotation 5, consequently can drive reaction section of thick bamboo 2 and rotate at annular frame 1 inner wall through support frame 3 when dwang 4 takes place to rotate.

Thus, the reaction cartridges 2 are driven to rotate around the rotation shaft 4, and the rotation shaft 4 is driven to rotate by the drive motor built in the drive mechanism 10, and then the rotation force is transmitted to the mixing cartridge 11 located in the reaction cartridge 2.

The rotating rod 4 is provided with a plurality of rotating shafts 5 coaxially inserted into the reaction cylinder 2, the rotating shafts 5 are inserted into the mixing cylinder 11, the rotating shafts 5 rotate together with the screw bodies 14, the outer side walls of the rotating shafts 5 are provided with the screw bodies 14 positioned in the stirring cavities 21, and the screw bodies 14 drive the pistons 18 to extrude the bovine bone collagen peptide and carbon dioxide mixture positioned in the compression cavities 20.

The mixing drum 11 is internally provided with a piston 18 in a sliding manner and is used for dividing the mixing drum 11 into a compression cavity 20 and an agitating cavity 21, the inner wall of the mixing drum 11 is provided with a first material-thinning hole 30 and a second material-thinning hole 31 which are mutually communicated, the first material-thinning hole 30 and the second material-thinning hole 31 are positioned on two sides of the piston 18, and an electromagnetic pump is arranged in the first material-thinning hole 30.

An end cover 12 which is movably arranged at one end of the mixing drum 11 and discharges bovine bone collagen peptide is arranged at one end of the mixing drum 11, the end cover 12 coaxially slides at the end of the mixing drum 11 through a sliding groove 35 and a limiting inserted link 34, the sliding groove 35 is arranged at the end of the mixing drum 11, a second electromagnetic generator 36 is arranged in the sliding groove 35, the limiting inserted link 34 is reset and stretches in the sliding groove 35 through a second reset spring 37, and a first magnet plate is arranged at one side of the limiting inserted link 34 facing the second electromagnetic generator 36

The first dredging hole 30 and the second dredging hole 31 are not in a communication state, and the second electromagnetic generator 36 is started to attract the limiting plunger 34 to enable the end cover 12 to block the mixing drum 11, so that bovine collagen peptide and carbon dioxide entering the mixing drum 11 are primarily mixed and stirred, and the rotation of the screw 14 can push the piston 18 to squeeze the bovine collagen peptide and carbon dioxide mixture in the compression cavity 20 through the rectangular rigid plunger 33, so that carbon dioxide is dissolved in water under high pressure, carbonic acid is generated, and the pH value is reduced.

The inner wall of the mixing cylinder 11 is fixed with a limit frame 32, the piston 18 is fixed with a rectangular rigid inserted rod 33 sliding on the limit frame 32, the rectangular rigid inserted rod 33 abuts against the spiral body 14, the rotation direction of the spiral body 14 faces the piston 18, the piston 18 is connected with the end cover 12 through the first return spring 19, and as the rectangular rigid inserted rod 33 abuts against the outer side wall of the spiral body 14, when the rectangular rigid inserted rod 33 is pushed away from the end of the spiral body 14, and the piston 18 cannot press the compression cavity 20 any more.

Then, during the continuous rotation of the screw 14, the rectangular rigid insert 33 is separated from the end of the screw 14, the piston 18 moves reversely under the action of the first return spring 19, the compression cavity 20 is not compressed, and then the rectangular rigid insert 33 is propped against the outer side wall of the screw 14 again, that is, the continuous mixing and stirring of the bovine bone collagen peptide and carbon dioxide in the stirring cavity 21 can be realized along with the rotation of the rotating shaft 5 along with the screw 14, and the continuous pressurization and pressure release of the mixture of the bovine bone collagen peptide and carbon dioxide in the compression cavity 20 can be realized.

The spiral body 14 is fixed with the tip board 15 that offsets with mixing drum 11 tip inner wall towards firm vent disc 23 one side, mixing drum 11 tip inner wall is provided with trigger portion 38, trigger portion 38 includes first trigger expansion point 381 and second trigger expansion point 382, the fillet has all been seted up to first trigger expansion point 381 and second trigger expansion point 382 tip, trigger portion 38 passes through electrical system and first electromagnetic generator 27, second electromagnetic generator 36 and electromagnetic pump link to each other, the first trigger expansion point 381 of passing electrical system is outstanding, the spiral body 14 that carries tip board 15 is crossing not outstanding second trigger expansion point 382 this moment, and press the withdrawal against first trigger expansion point 381, the second trigger expansion point 382 at this moment is outstanding, piston 18 compression chamber 20 at this moment is to unable the compression state of continuing.

Then the electronic control system turns off the second electromagnetic generator 36 to enable the end cover 12 not to block the mixing drum 11 any more, the compression cavity 20 at high pressure is released rapidly, the mixture of bovine bone collagen peptide and carbon dioxide in the compression cavity 20 is released, and carbon dioxide is dissolved in water under high pressure to generate carbonic acid, so that the pH value is reduced.

The pressure is then reduced rapidly after penetration into the microbial cells, causing the cells to rupture and produce a burst effect, thereby killing bacteria, yeasts and molds, and the second electromagnetic generator 36 is then re-opened and the end cap 12 will repeatedly close the end of the mixing drum 11.

The outer side wall of the mixing drum 11 is provided with a buffer tank 13, the buffer tank 13 is communicated with the mixing drum 11 through a communication hole 25, the buffer tank 13 is an elastic tank, a first communication pipe 22 is arranged on the buffer tank 13, the outer side wall of the mixing drum 11 slides with a baffle ring 26 for blocking the communication hole 25, a first electromagnetic generator 27 is further fixed in the buffer tank 13, the baffle ring 26 slides through a limiting rod 28 fixed on the first electromagnetic generator 27, an end magnetic block 29 is arranged at the sliding end part of the limiting rod 28, and a second magnet plate is arranged on one side of the baffle ring 26 towards the first electromagnetic generator 27.

The electromagnetic pump is started to enable the first material-thinning hole 30 to be communicated with the second material-thinning hole 31, the first electromagnetic generator 27 is started to generate a magnetic field identical to that of the second magnet plate on the baffle ring 26, the baffle ring 26 is pushed to block the communication hole 25, the piston 18 moves reversely under the action of the first reset spring 19, so that the bovine bone collagen peptide and carbon dioxide mixture originally existing in the stirring cavity 21 are extruded into the compression cavity 20 through the first material-thinning hole 30 and the second material-thinning hole 31, when the rectangular rigid inserting rod 33 is propped against the outer side wall of the spiral body 14 again, the electromagnetic pump is closed to block the flow channels of the first material-thinning hole 30 and the second material-thinning hole 31, the first electromagnetic generator 27 is closed, and the end magnetic block 29 is pushed to push the baffle ring 26 with the second magnet plate to expose the communication hole 25, so that subsequent material supplementing is facilitated.

Then, in the process of rotating the screw 14 for one turn, the screw 14 with the end plate 15 firstly touches the protruding second triggering telescopic point 382, then the second triggering telescopic point 382 is pressed and retracted, and then the peripheral pump is started, so that bovine bone collagen peptide is fed through the bovine bone collagen peptide input pipe 6 and carbon dioxide through the carbon dioxide input pipe 7, and then the peripheral pump is closed.

Finally, the bottom of the reaction cylinder 2 is provided with a bovine bone collagen peptide discharge pipe 9, the top of the side wall of the reaction cylinder 2 is provided with a carbon dioxide discharge pipe 8, and as the reaction cylinder 2 rotates on the inner wall of the annular frame 1 through the supporting frame 3, the bovine bone collagen peptide and carbon dioxide mixture can be effectively separated through centrifugal force, the bovine bone collagen peptide after sterilization can be discharged from the bovine bone collagen peptide discharge pipe 9, and carbon dioxide can be discharged from the carbon dioxide discharge pipe 8 at the top of the side wall of the reaction cylinder 2.

The working principle of the invention is as follows:

Firstly, pumping bovine bone collagen peptide into a buffer box 13 through a bovine bone collagen peptide input pipe 6 and a rubber hose, then enabling the bovine bone collagen peptide to enter a mixing cylinder 11 through a communication hole 25, pumping carbon dioxide into a stable ventilation disk 23 through a carbon dioxide input pipe 7 and the rubber hose, enabling the carbon dioxide in the stable ventilation disk 23 to enter a ventilation hole 16 through an air inlet hole 17 on a rotating shaft 5, and then enabling the carbon dioxide to reach the mixing cylinder 11, thus completing the effect of introducing the bovine bone collagen peptide and the carbon dioxide into the mixing cylinder 11;

S2, driving the rotating rod 4 to rotate by starting an external driving mechanism, wherein the driving mechanism 10 arranged on the rotating rod 4 and the driving mechanism 10 are connected with the reaction cylinder 2 through a rotating shaft 5, so that the reaction cylinder 2 can be driven to rotate on the inner wall of the annular frame 1 through the supporting frame 3 when the rotating rod 4 rotates, a plurality of reaction cylinders 2 are driven to rotate around the rotating rod 4, meanwhile, a driving motor arranged in the driving mechanism 10 drives the rotating rod 4 to rotate, and then the rotating force is transmitted into a mixing cylinder 11 positioned in the reaction cylinder 2;

s3, the rotating shaft 5 rotates together with the spiral body 14, the first material thinning hole 30 and the second material thinning hole 31 are not in a communicating state, the second electromagnetic generator 36 starts to attract the limiting inserted rod 34 to enable the end cover 12 to block the mixing drum 11, so that bovine bone collagen peptide and carbon dioxide entering the mixing drum 11 are primarily mixed and stirred, the rotation of the spiral body 14 can push the piston 18 to press the mixture of bovine bone collagen peptide and carbon dioxide in the compression cavity 20 through the rectangular rigid inserted rod 33, so that carbon dioxide is dissolved in water under high pressure to form carbonic acid and reduce pH value, then, as the rectangular rigid inserted rod 33 is propped against the outer side wall of the spiral body 14, when the rectangular rigid inserted rod 33 is pushed to the end part of the spiral body 14, and the piston 18 can not be pushed to compress the compression cavity 20 any more, then, the rectangular rigid inserted rod 33 can be separated from the end part of the spiral body 14, the piston 18 moves reversely under the action of the first reset spring 19, the compression cavity 20 is not compressed any more, and then the rectangular rigid inserted rod 33 can be propped against the outer side wall of the spiral body 14 again, namely, the mixed and the mixed bovine bone collagen peptide and the carbon dioxide can be compressed and the carbon dioxide can be stirred and the mixed collagen peptide can be compressed with the carbon dioxide under the compression of the condition that the compression cavity 20 is not broken along with the rotation of the spiral body 14, and the bovine bone collagen peptide can be compressed by the compression of the compression cavity 20 due to the fact that the rotation of the carbon dioxide is realized;

S4, protruding the first trigger expansion point 381 through an electric control system, wherein the screw 14 carrying the end plate 15 passes through the second trigger expansion point 382 which is not protruding, and presses and retracts against the first trigger expansion point 381, the second trigger expansion point 382 protrudes, and the piston 18 compresses the compression cavity 20 to a state that compression cannot be continued;

S5, the electronic control system turns off the second electromagnetic generator 36 to enable the end cover 12 not to block the mixing drum 11 any more, the compression cavity 20 at high pressure is released rapidly at the moment, the bovine bone collagen peptide and carbon dioxide mixture in the compression cavity 20 is released, carbon dioxide is dissolved in water under high pressure to generate carbonic acid, the pH value is reduced, then the carbonic acid permeates into microbial cells and then is rapidly depressurized, the cells are broken to generate a blasting effect, bacteria, yeast and mold are killed, then the second electromagnetic generator 36 is turned on again, and the end cover 12 is repeatedly blocked at the end of the mixing drum 11;

S6, starting an electromagnetic pump to enable the first material-thinning hole 30 to be communicated with the second material-thinning hole 31, starting the first electromagnetic generator 27 to generate a magnetic field identical to that of the second magnet plate on the baffle ring 26, pushing the baffle ring 26 to block the communication hole 25, and under the action of the first reset spring 19, enabling the piston 18 to move reversely, so that the bovine bone collagen peptide and carbon dioxide mixture originally existing in the stirring cavity 21 are extruded into the compression cavity 20 through the first material-thinning hole 30 and the second material-thinning hole 31, when the rectangular rigid inserting rod 33 is propped against the outer side wall of the spiral body 14 again, closing the electromagnetic pump to block the flow channels of the first material-thinning hole 30 and the second material-thinning hole 31, simultaneously closing the first electromagnetic generator 27, and pushing the baffle ring 26 with the second magnet plate by the end magnet 29 to expose the communication hole 25, so that subsequent material supplementing is facilitated;

And S7, in the process of rotating the screw 14 for one circle, as the screw 14 with the end plate 15 firstly touches the protruding second triggering expansion point 382, then the second triggering expansion point 382 is pressed and retracted, and then an external pump is started, so that bovine bone collagen peptide is fed through the bovine bone collagen peptide input pipe 6 and carbon dioxide through the carbon dioxide input pipe 7, and then the external pump is closed, finally, as the reaction cylinder 2 rotates on the inner wall of the annular frame 1 through the support frame 3, the bovine bone collagen peptide and carbon dioxide mixture can be effectively separated through centrifugal force, and the bovine bone collagen peptide with sterilization completion can be discharged from the bovine bone collagen peptide discharge pipe 9, and carbon dioxide can be discharged from the carbon dioxide discharge pipe 8 at the top of the side wall of the reaction cylinder 2.

The foregoing is only a preferred embodiment of the present invention, but the scope of the present invention is not limited thereto, and any person skilled in the art, who is within the scope of the present invention, should make equivalent substitutions or modifications according to the technical scheme of the present invention and the inventive concept thereof, and should be covered by the scope of the present invention.

Claims (10)

1. The bovine bone collagen peptide quick sterilization device comprises two annular frames and a rotating rod coaxially arranged with the annular frames, wherein the two annular frames are coaxially arranged up and down, the quick sterilization device is characterized in that a plurality of reaction cylinders are coaxially arranged in the annular frames and are circumferentially arranged, the reaction cylinder rotates on the inner wall of the annular frame through the supporting frame, a bovine bone collagen peptide input pipe and a carbon dioxide input pipe which are used for leading bovine bone collagen peptide and carbon dioxide into the mixing cylinder are arranged on the reaction cylinder, a plurality of mixing cylinders are arranged in the reaction cylinder, and the mixing cylinders are linearly fixed in the reaction cylinder through a cylinder bracket;

The rotating rod is provided with a plurality of rotating shafts which are coaxially inserted into the reaction cylinder, the rotating shafts are inserted into the mixing cylinder, the piston is arranged in the mixing cylinder in a sliding mode, the mixing cylinder is divided into a compression cavity and an stirring cavity, the outer side wall of the rotating shaft is provided with a spiral body positioned in the stirring cavity, the spiral body drives the piston to extrude the bovine bone collagen peptide and carbon dioxide mixture positioned in the compression cavity, and one end of the mixing cylinder is provided with an end cover which is movably arranged and discharges the bovine bone collagen peptide.

2. The bovine bone collagen peptide rapid sterilization device according to claim 1, wherein a plurality of driving mechanisms are arranged on the rotating rod along the shaft, the driving mechanisms comprise a plurality of driving motors, the driving motors are in one-to-one correspondence with the reaction cylinders, and the output ends of the driving motors are coaxially fixed with the rotating shaft.

3. The bovine bone collagen peptide rapid sterilization device according to claim 2, wherein a limit frame is fixed on the inner wall of the mixing cylinder, a rectangular rigid insert rod sliding on the limit frame is fixed on the piston, the rectangular rigid insert rod is abutted against the screw body, the rotation direction of the screw body faces the piston, and the piston is connected with the end cover through a first return spring.

4. The bovine bone collagen peptide rapid sterilization device according to claim 3, wherein the end cover coaxially slides at the end of the mixing drum through a sliding groove and a limiting inserted bar, the sliding groove is formed at the end of the mixing drum, a second electromagnetic generator is arranged in the sliding groove, the limiting inserted bar is reset and stretches in the sliding groove through a second reset spring, and a first magnet plate is arranged at one side of the limiting inserted bar facing the second electromagnetic generator.

5. The bovine bone collagen peptide rapid sterilization device according to claim 4, wherein the inner wall of the mixing cylinder is provided with a first material-thinning hole and a second material-thinning hole which are communicated with each other, the first material-thinning hole and the second material-thinning hole are positioned on two sides of the piston, and an electromagnetic pump is arranged in the first material-thinning hole.

6. The bovine bone collagen peptide rapid sterilization device according to claim 5, wherein the mixing drum is coaxially fixed with a stable ventilation disc, the stable ventilation disc is inserted with a second communication pipe, a ventilation hole communicated with the stirring cavity is formed in the rotating shaft, and the stable ventilation disc is communicated with the ventilation hole through an air inlet hole.

7. The bovine bone collagen peptide quick sterilization device according to claim 6, wherein a buffer box is arranged on the outer side wall of the mixing drum, the buffer box is communicated with the mixing drum through a communication hole, the buffer box is an elastic box, a baffle ring for blocking the communication hole is arranged on the outer side wall of the mixing drum in a sliding manner, a first electromagnetic generator is further fixed in the buffer box, the baffle ring slides through a limiting rod fixed on the first electromagnetic generator, an end magnetic block is arranged at the sliding end part of the limiting rod, a second magnetic plate is arranged on one side of the baffle ring, facing the first electromagnetic generator, of the buffer box, and a first communication pipe is arranged on the buffer box.

8. The bovine bone collagen peptide rapid sterilization device according to claim 7, wherein the bovine bone collagen peptide input pipe is communicated with the first communication pipe through a rubber hose, the carbon dioxide input pipe is communicated with the second communication pipe through a rubber hose, the bovine bone collagen peptide discharge pipe is arranged at the bottom of the reaction cylinder, and the carbon dioxide discharge pipe is arranged at the top of the side wall of the reaction cylinder.

9. The bovine bone collagen peptide rapid sterilization device according to claim 8, wherein an end plate which is abutted against the inner wall of the end part of the mixing drum is fixed on one side of the spiral body, which faces the stable ventilation disk, the inner wall of the end part of the mixing drum is provided with a triggering part, the triggering part comprises a first triggering telescopic point and a second triggering telescopic point, round corners are formed at the ends of the first triggering telescopic point and the second triggering telescopic point, and the triggering part is connected with the first electromagnetic generator, the second electromagnetic generator and the electromagnetic pump through an electric control system.

10. The sterilization method of the bovine bone collagen peptide rapid sterilization device, which is applied to the bovine bone collagen peptide rapid sterilization device in claim 9, is characterized by comprising the following specific operation steps:

firstly, pumping bovine bone collagen peptide into a buffer box through a bovine bone collagen peptide input pipe and a rubber hose, then enabling the bovine bone collagen peptide to enter a mixing cylinder through a communication hole, and pumping carbon dioxide into a stable ventilation disc through a carbon dioxide input pipe and the rubber hose to finish the effect of introducing the bovine bone collagen peptide and the carbon dioxide into the mixing cylinder;

S2, driving the rotating rod to rotate, wherein the rotating rod can drive the reaction cylinder to rotate on the inner wall of the annular frame through the support frame when rotating, and meanwhile, a driving motor arranged in the driving mechanism drives the rotating rod to rotate, and the rotating force is transmitted into a mixing cylinder positioned in the reaction cylinder;

s3, rotating the rotating shaft with the screw body to rotate together, primarily mixing and stirring the bovine collagen peptide and the carbon dioxide, and extruding and compressing the mixture of the bovine collagen peptide and the carbon dioxide in the cavity by the piston to dissolve the carbon dioxide in water under high pressure so as to realize carbonic acid dissolution and pH value reduction;

s4, protruding a first trigger expansion point through an electric control system, enabling the screw body carrying the end plate to pass through a second trigger expansion point which is not protruding at the moment, pressing and retracting the screw body against the first trigger expansion point, protruding the second trigger expansion point at the moment, and enabling the piston to compress the compression cavity to a state that compression cannot be continued;

S5, the electric control system turns off the second electromagnetic generator, releases the mixture of bovine collagen peptide and carbon dioxide in the compression cavity, and rapidly decompresses after penetrating into microbial cells, so that the cells are broken to generate a blasting effect, and bacteria, yeast and mould are killed;

S6, starting an electromagnetic pump to enable the first material-thinning holes to be communicated with the second material-thinning holes, and extruding the mixture of bovine bone collagen peptide and carbon dioxide which originally exist in the stirring cavity into the compression cavity through the first material-thinning holes and the second material-thinning holes;

And S7, then, the second triggering telescopic point is pressed for retraction, and then, an external pump is started, so that bovine bone collagen peptide is fed through the bovine bone collagen peptide input pipe and carbon dioxide through the carbon dioxide input pipe, the bovine bone collagen peptide after sterilization is discharged from the bovine bone collagen peptide discharge pipe, and carbon dioxide is discharged from the carbon dioxide discharge pipe at the top of the side wall of the reaction cylinder.