A rapid sterilization device and method for bovine bone collagen peptide

Abstract

The present application relates to the technical field of sterilization, and discloses a kind of fast sterilization device and sterilization method of bovine bone collagen peptide, including two annular frames and the rotating rod coaxially arranged with annular frame, two annular frames are coaxially arranged, multiple reaction cylinders are coaxially arranged in annular frame, reaction cylinder rotates in annular frame wall by support frame, reaction cylinder is provided with bovine bone collagen peptide input pipe and carbon dioxide input pipe that bovine bone collagen peptide and carbon dioxide are passed into mixing cylinder.The electric control system of the present application closes the second electromagnetic generator, so that the end cap no longer blocks the mixing cylinder. At this time, the compressed chamber under high pressure will be quickly released, releasing the mixture of bovine bone collagen peptide and carbon dioxide in the compressed chamber. Carbon dioxide dissolves in water under high pressure to form carbonic acid, reducing the pH value, and then penetrates into microbial cells and rapidly decompresses, causing cell rupture and a blasting effect, thereby killing bacteria, yeast and mold.

Description

TECHNICAL FIELD

[0001] The present application relates to the technical field of sterilization, in particular to a rapid sterilization device and method for bovine bone collagen peptide. BACKGROUND

[0002] Bovine bone collagen peptide is sensitive to heat, and traditional heat sterilization methods (such as high-temperature instantaneous sterilization) can easily cause denaturation, inactivation, Maillard reaction and undesirable flavors, so it is necessary to have the following characteristics: low temperature: the whole process is carried out at low temperature or instantaneous medium temperature, usually less than 65°C, to prevent collagen peptide from denaturation, so the conventional heating sterilization method is not suitable for the sterilization of bovine bone collagen peptide, therefore the sterilization of bovine bone collagen peptide usually adopts non-heating sterilization method, but the above sterilization and disinfection has the following problems:

[0003] Firstly, in order to avoid high temperature leading to inactivation of bovine bone collagen peptide, ultraviolet lamp is used to kill the microbial cells in bovine bone collagen peptide, secondly, this direct use of ultraviolet disinfection cannot achieve full coverage of bovine bone collagen peptide, therefore it is necessary to continuously stir the area which cannot be irradiated by ultraviolet light to disinfect, which undoubtedly reduces the disinfection efficiency.

[0004] Therefore, we design a rapid sterilization device and method for bovine bone collagen peptide. SUMMARY

[0005] The purpose of the present application is to solve the problem of inactivation of bovine bone collagen peptide caused by high temperature in the prior art, and to provide a rapid sterilization device and method for bovine bone collagen peptide.

[0006] In order to achieve the above purpose, the present application adopts the following technical scheme:

[0007] A rapid sterilization device for bovine bone collagen peptide, comprising two annular frames and a rotating rod coaxially arranged with the annular frames, the two annular frames are coaxially arranged, a plurality of reaction cylinders are coaxially arranged in the annular frame, the plurality of reaction cylinders are arranged in a circle, the reaction cylinder rotates on the inner wall of the annular frame through a support frame, the reaction cylinder is provided with a bovine bone collagen peptide input pipe and a carbon dioxide input pipe for feeding bovine bone collagen peptide and carbon dioxide into the mixing cylinder, a plurality of mixing cylinders are arranged in the reaction cylinder and fixed in the reaction cylinder through a cylinder support;

[0008] The rotating rod is provided with a plurality of rotating shafts coaxially inserted into the reaction cylinder, the rotating shafts are inserted into the mixing cylinder, a piston is slidably arranged in the mixing cylinder and is used to divide the mixing cylinder into a compression cavity and an agitation cavity, a spiral body is arranged on the outer side wall of the rotating shaft and located in the agitation cavity, the spiral body drives the piston to extrude the mixture of the bovine bone collagen peptide and carbon dioxide in the compression cavity, and an end cover is arranged at one end of the mixing cylinder and is used to discharge the bovine bone collagen peptide.

[0009] Preferably, a plurality of driving mechanisms are arranged on the rotating rod along the shaft, the driving mechanisms include a plurality of driving motors, the driving motors are in one-to-one correspondence with the reaction cylinders, and output ends of the driving motors are coaxially fixed with the rotating shafts.

[0010] Preferably, a limiting frame is fixed to the inner wall of the mixing cylinder, a rectangular rigid insertion rod that slides on the limiting frame is fixed to the piston, the rectangular rigid insertion rod abuts against the spiral body, the spiral body rotates towards the piston, and the piston is connected with the end cover through a first return spring.

[0011] Preferably, the end cover coaxially slides at the end of the mixing cylinder through a sliding groove and a limiting insertion rod, the sliding groove is arranged at the end of the mixing cylinder, a second electromagnetic generator is arranged in the sliding groove, the limiting insertion rod is reset and retracted in the sliding groove through a second return spring, and a first magnet plate is arranged on the side of the limiting insertion rod that faces the second electromagnetic generator.

[0012] Preferably, a first material dispersing hole and a second material dispersing hole that are in communication with each other are arranged in the inner wall of the mixing cylinder, the first material dispersing hole and the second material dispersing hole are located on both sides of the piston, and an electromagnetic pump is arranged in the first material dispersing hole.

[0013] Preferably, a stable aeration disc is coaxially fixed to the mixing cylinder, a second communication pipe is inserted into the stable aeration disc, an aeration hole that is in communication with the agitation cavity is arranged on the rotating shaft, and the stable aeration disc is in communication with the aeration hole through the air inlet hole.

[0014] Preferably, a buffer tank is arranged on the outer side wall of the mixing cylinder, the buffer tank is in communication with the mixing cylinder through a communication hole, the buffer tank is an elastic tank, a blocking ring that is used to block the communication hole is slidably arranged on the outer side wall of the mixing cylinder, a first electromagnetic generator is further fixed in the buffer tank, the blocking ring slides through a limiting rod fixed on the first electromagnetic generator, an end magnetic block is arranged on the sliding end of the limiting rod, a second magnet plate is arranged on the side of the blocking ring that faces the first electromagnetic generator, and a first communication pipe is arranged on the buffer tank.

[0015] Preferably, a bovine bone collagen peptide input pipe is in communication with the first communication pipe through a rubber hose, a carbon dioxide input pipe is in communication with the second communication pipe through a rubber hose, a bovine bone collagen peptide discharge pipe is arranged at the bottom of the reaction cylinder, and a carbon dioxide discharge pipe is arranged at the top of the side wall of the reaction cylinder.

[0016] Preferably, the spiral body is fixed with an end plate on the side facing the stable aeration disc, the end of the mixing cylinder is provided with a trigger part, the trigger part includes a first trigger expansion point and a second trigger expansion point, the first trigger expansion point and the second trigger expansion point are both provided with a rounded corner at the end, and the trigger part is connected with the first electromagnetic generator, the second electromagnetic generator and the electromagnetic pump through an electric control system.

[0017] A sterilization method of a rapid sterilization device for bovine collagen peptide, the specific operation steps are as follows:

[0018] S1: First, let the bovine collagen peptide pass through the bovine collagen peptide input pipe and the rubber hose to pump into the buffer box, then this part of the bovine collagen peptide enters the mixing cylinder through the communication hole, and the carbon dioxide is pumped into the stable aeration disc through the carbon dioxide input pipe and the rubber hose, and the function of introducing the bovine collagen peptide and the carbon dioxide into the mixing cylinder is completed;

[0019] S2: Then drive the rotating rod to rotate, which can drive the reaction cylinder to rotate in the inner wall of the annular frame through the support frame, and the driving motor built in the driving mechanism drives the rotating rod to rotate, and the rotating force is transmitted to the mixing cylinder in the reaction cylinder;

[0020] S3: The rotating shaft rotates with the spiral body, the bovine collagen peptide and the carbon dioxide are preliminarily mixed and stirred, the piston extrudes the bovine collagen peptide and carbon dioxide mixture in the compression cavity, so as to realize that the carbon dioxide dissolves in water to generate carbonic acid under high pressure and reduce the pH value;

[0021] S4: The first trigger expansion point is protruded through the electric control system, at this time, the spiral body carrying the end plate passes the second trigger expansion point which is not protruded and presses against the first trigger expansion point, at this time, the second trigger expansion point is protruded, and the piston compresses the compression cavity to a state that it cannot continue to compress;

[0022] S5: Then the electric control system closes the second electromagnetic generator, releases the bovine collagen peptide and carbon dioxide mixture in the compression cavity, then penetrates into the microbial cells and rapidly reduces the pressure, causes the cells to rupture and produces a blasting effect, so as to kill bacteria, yeast and mold;

[0023] S6: Then the electromagnetic pump is started to make the first and second material discharge holes communicate, and the bovine collagen peptide and carbon dioxide mixture originally in the stirring cavity are extruded into the compression cavity through the first and second material discharge holes;

[0024] S7: Then the second trigger telescopic point is pressed to retract, and then the peripheral pump is started to allow the bovine collagen peptide to be fed through the bovine collagen peptide input pipe and the carbon dioxide to be fed through the carbon dioxide input pipe, the sterilized bovine collagen peptide is discharged from the bovine collagen peptide discharge pipe, and the carbon dioxide is discharged from the carbon dioxide discharge pipe at the top of the side wall of the reaction cylinder.

[0025] The beneficial effects of the present application are:

[0026] 1、In the present application, the helix continues to rotate, and the rectangular rigid insertion rod is separated from the end of the helix. Under the action of the first return spring, the piston moves reversely and no longer compresses the compression cavity. Then the rectangular rigid insertion rod re-contacts the outer lateral wall of the helix, that is, the rotation shaft rotates together with the helix to realize the continuous mixing and stirring of the bovine collagen peptide and carbon dioxide in the stirring cavity, and the continuous pressurization and decompression of the bovine collagen peptide and carbon dioxide mixture in the compression cavity.

[0027] 2、In the present application, the electric control system turns off the second electromagnetic generator, so that the end cover no longer blocks the mixing cylinder. At this time, the compression cavity under high pressure is quickly released, and the bovine collagen peptide and carbon dioxide mixture in the compression cavity is released. Carbon dioxide dissolves in water to generate carbonic acid under high pressure, reduces the pH value, then penetrates into the microbial cells and rapidly decompresses, causing cell rupture and explosion effect, thereby killing bacteria, yeast and mold. BRIEF DESCRIPTION OF DRAWINGS

[0028] Figure 1 A structural schematic diagram of a bovine collagen peptide rapid sterilization device is provided for the present application;

[0029] Figure 2 A structural schematic diagram of a reaction cylinder in a bovine collagen peptide rapid sterilization device is provided for the present application;

[0030] Figure 3 A main sectional view of a reaction cylinder in a bovine collagen peptide rapid sterilization device is provided for the present application;

[0031] Figure 4 A first state structural schematic diagram of a mixing cylinder in a bovine collagen peptide rapid sterilization device is provided for the present application;

[0032] Figure 5 A structural schematic diagram of the left and right isometric axis side view of a mixing cylinder in a bovine collagen peptide rapid sterilization device is provided for the present application; Figure 4 An enlarged structural schematic diagram of position A in the above-mentioned isometric axis side view is provided for the present application;

[0033] Figure 6 A structural schematic diagram of the left and right isometric axis side view of a mixing cylinder in a bovine collagen peptide rapid sterilization device is provided for the present application;

[0034] Figure 7A first state main sectional view of a mixing cylinder in a fast sterilization device for bovine bone collagen peptide is provided in the application;

[0035] Figure 8 For Figure 7 The structure of B in the middle is enlarged and schematically shown.

[0036] Figure 9 A structure diagram of a spiral body in a fast sterilization device for bovine bone collagen peptide is provided in the application;

[0037] Figure 10 A second state structure diagram of a mixing cylinder in a fast sterilization device for bovine bone collagen peptide is provided in the application;

[0038] Figure 11 A second state main sectional view of a mixing cylinder in a fast sterilization device for bovine bone collagen peptide is provided in the application;

[0039] Figure 12 A structure diagram of a trigger part in a fast sterilization device for bovine bone collagen peptide is provided in the application.

[0040] In the figure: 1, annular frame; 2, reaction cylinder; 3, support frame; 4, rotating rod; 5, rotating shaft; 6, bovine bone collagen peptide input pipe; 7, carbon dioxide input pipe; 8, carbon dioxide discharge pipe; 9, bovine bone collagen peptide discharge pipe; 10, driving mechanism; 11, mixing cylinder; 12, end cover; 13, buffer tank; 14, spiral body; 15, end plate; 16, air hole; 17, air inlet hole; 18, piston; 19, first return spring; 20, compression cavity; 21, stirring cavity; 22, first communication pipe; 23, stable air disc; 24, second communication pipe; 25, communication hole; 26, retaining ring; 27, first electromagnetic generator; 28, limiting rod; 29, end magnetic block; 30, first sparse hole; 31, second sparse hole; 32, limiting frame; 33, rectangular rigid insertion rod; 34, limiting insertion rod; 35, sliding groove; 36, second electromagnetic generator; 37, second return spring;

[0041] 38, trigger part; 381, first trigger telescopic point; 382, second trigger telescopic point. DETAILED DESCRIPTION

[0042] Referring to Figures 1-12 A fast sterilization device for bovine bone collagen peptide, comprising two annular frames 1 and a rotating rod 4 coaxially arranged with the annular frames 1, the two annular frames 1 are coaxially arranged above and below, a plurality of reaction cylinders 2 are coaxially arranged in the annular frames 1, the plurality of reaction cylinders 2 are arranged in a circle, and the reaction cylinders 2 rotate on the inner wall of the annular frames 1 through support frames 3 to provide driving force for the rotation of the reaction cylinders 2.

[0043] The reaction cylinder 2 is provided with a bovine bone collagen peptide input pipe 6 and a carbon dioxide input pipe 7 for feeding bovine bone collagen peptide and carbon dioxide into the mixing cylinder 11, and a plurality of mixing cylinders 11 are fixed in the reaction cylinder 2 in a linear manner through a cylinder support.

[0044] The bovine bone collagen peptide is pumped into the buffer box 13 through the bovine bone collagen peptide input pipe 6 and the rubber hose, and then enters the mixing cylinder 11 through the communication hole 25. The mixing cylinder 11 is coaxially fixed with a stable aeration disc 23, and the second communication pipe 24 is inserted into the stable aeration disc 23. The bovine bone collagen peptide input pipe 6 is communicated with the first communication pipe 22 through the rubber hose, and the carbon dioxide input pipe 7 is communicated with the second communication pipe 24 through the rubber hose. The aeration hole 16 is provided in the rotating shaft 5 and communicated with the stirring cavity 21. The stable aeration disc 23 is communicated with the aeration hole 16 through the air inlet hole 17. The carbon dioxide is pumped into the stable aeration disc 23 through the carbon dioxide input pipe 7 and the rubber hose, and then enters the aeration hole 16 through the air inlet hole 17 of the rotating shaft 5, and then enters the mixing cylinder 11, so as to complete the feeding of bovine bone collagen peptide and carbon dioxide into the mixing cylinder 11.

[0045] A plurality of driving mechanisms 10 are arranged on the rotating rod 4 along the shaft. The driving mechanism 10 includes a plurality of driving motors, and the driving motor is coaxially fixed with the rotating shaft 5. The driving mechanism is turned on to drive the rotating rod 4 to rotate. Since the driving mechanism 10 is arranged on the rotating rod 4 and connected with the reaction cylinder 2 through the rotating shaft 5, the rotating rod 4 can drive the reaction cylinder 2 to rotate on the inner wall of the annular frame 1 through the support frame 3.

[0046] Therefore, the plurality of reaction cylinders 2 are driven to rotate around the rotating rod 4, and the driving motor in the driving mechanism 10 drives the rotating rod 4 to rotate, and then the rotating force is transmitted to the mixing cylinder 11 in the reaction cylinder 2.

[0047] A plurality of rotating shafts 5 are arranged on the rotating rod 4 and coaxially inserted into the reaction cylinder 2. The rotating shaft 5 is inserted into the mixing cylinder 11. The rotating rotating shaft 5 rotates with the spiral body 14. The rotating shaft 5 is provided with the spiral body 14 in the stirring cavity 21. The spiral body 14 drives the piston 18 to extrude the bovine bone collagen peptide and carbon dioxide mixture in the compression cavity 20.

[0048] The piston 18 slides in the mixing cylinder 11 and separates the mixing cylinder 11 into the compression cavity 20 and the stirring cavity 21. The first and second material discharge holes 30 and 31 are provided in the inner wall of the mixing cylinder 11 and communicated with each other, and the first and second material discharge holes 30 and 31 are located on both sides of the piston 18. The first material discharge hole 30 is provided with an electromagnetic pump.

[0049] The mixing barrel 11 is provided with an end cover 12 movably arranged at one end of the mixing barrel 11 and discharging the collagen peptide of cattle bone. The end cover 12 is coaxially slid at the end of the mixing barrel 11 through a sliding groove 35 and a limiting plug 34. The sliding groove 35 is arranged at the end of the mixing barrel 11, and a second electromagnetic generator 36 is arranged in the sliding groove 35. The limiting plug 34 is reset in the sliding groove 35 through a second reset spring 37. The limiting plug 34 is provided with a first magnet plate on the side facing the second electromagnetic generator 36.

[0050] The first and second material sparse holes 30 and 31 are not in a communication state, and the second electromagnetic generator 36 is turned on to attract the limiting plug 34, so that the end cover 12 blocks the mixing barrel 11. Therefore, the collagen peptide of cattle bone and carbon dioxide entering the mixing barrel 11 are preliminarily mixed and stirred. Since the rotation of the spiral body 14 can push the piston 18 to extrude and compress the mixture of the collagen peptide of cattle bone and carbon dioxide in the compression cavity 20 through the rectangular rigid plug 33, carbon dioxide is dissolved in water to generate carbonic acid under high pressure and reduce the pH value.

[0051] The mixing barrel 11 is provided with a limiting frame 32 fixed on the inner wall. The piston 18 is fixed with a rectangular rigid plug 33 sliding in the limiting frame 32. The rectangular rigid plug 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 a first reset spring 19. Since the rectangular rigid plug 33 abuts against the outer side wall of the spiral body 14, when the rectangular rigid plug 33 is pushed away from the end of the spiral body 14, the piston 18 cannot extrude the compression cavity 20 any more.

[0052] Then, during the continuous rotation of the spiral body 14, the rectangular rigid plug 33 will be separated from the end of the spiral body 14. Under the action of the first reset spring 19, the piston 18 moves reversely and no longer compresses the compression cavity 20. Then, the rectangular rigid plug 33 abuts against the outer side wall of the spiral body 14 again. That is, the rotation of the rotating shaft 5 with the spiral body 14 can realize the continuous mixing and stirring of the collagen peptide of cattle bone and carbon dioxide in the stirring cavity 21, and the continuous pressurization and decompression of the mixture of the collagen peptide of cattle bone and carbon dioxide in the compression cavity 20.

[0053] The helix 14 is fixed with an end plate 15 on the side facing the stable ventilation disc 23, the end plate 15 abuts against the inner wall of the end of the mixing cylinder 11, the inner wall of the end of the mixing cylinder 11 is provided with a trigger part 38, the trigger part 38 includes a first trigger telescopic point 381 and a second trigger telescopic point 382, the ends of the first trigger telescopic point 381 and the second trigger telescopic point 382 are both provided with a rounded corner, the trigger part 38 is connected with the first electromagnetic generator 27, the second electromagnetic generator 36 and the electromagnetic pump through an electric control system, the first trigger telescopic point 381 is protruded through the electric control system, at this time, the helix 14 carrying the end plate 15 is compressed by pressing against the first trigger telescopic point 381 after passing the second trigger telescopic point 382 which is not protruded, at this time, the second trigger telescopic point 382 is protruded, and the piston 18 is compressed to a state that it cannot continue to be compressed.

[0054] Then the electric control system closes the second electromagnetic generator 36, so that the end cover 12 no longer blocks the mixing cylinder 11, at this time, the compression cavity 20 under high pressure is quickly released, and the mixture of the bovine collagen peptide and the carbon dioxide in the compression cavity 20 is released, the carbon dioxide dissolves in water to generate carbonic acid under high pressure, and the pH value is reduced.

[0055] Then the mixture penetrates into the microbial cells and rapidly depressurizes, causing the cells to rupture and produce a blasting effect, thereby killing bacteria, yeast and mold, and then the second electromagnetic generator 36 is reopened, and the end cover 12 repeatedly blocks the end of the mixing cylinder 11.

[0056] The outer side wall of the mixing cylinder 11 is provided with a buffer tank 13, the buffer tank 13 is communicated with the mixing cylinder 11 through a communication hole 25, the buffer tank 13 is an elastic tank, the buffer tank 13 is provided with a first communication pipe 22, the outer side wall of the mixing cylinder 11 is slidably provided with a blocking ring 26 for blocking the communication hole 25, the buffer tank 13 is further fixed with a first electromagnetic generator 27, the blocking ring 26 is slidably provided with a limiting rod 28 fixed on the first electromagnetic generator 27, and the limiting rod 28 is provided with an end magnetic block 29 at the sliding end, and the blocking ring 26 is provided with a second magnet plate on the side facing the first electromagnetic generator 27.

[0057] The electromagnetic pump is opened to make the first material hole 30 and the second material hole 31 communicate, and the first electromagnetic generator 27 is opened at the same time, a magnetic field same as the second magnet plate on the blocking ring 26 is generated, the blocking ring 26 is pushed to block the communication hole 25, under the action of the first return spring 19, the piston 18 moves reversely, thereby the mixture of the bovine collagen peptide and the carbon dioxide originally existing in the stirring cavity 21 is squeezed into the compression cavity 20 through the first material hole 30 and the second material hole 31, when the rectangular rigid inserting rod 33 re-contacts the outer side wall of the helix 14, the electromagnetic pump is closed to block the flow channel of the first material hole 30 and the second material hole 31, and the first electromagnetic generator 27 is closed, the end magnetic block 29 pushes the blocking ring 26 with the second magnet plate to expose the communication hole 25, thereby facilitating the subsequent material supplementing.

[0058] Then, as the helix 14 rotates one circle, the helix 14 with the end plate 15 will first touch the protruding second trigger telescopic point 382, then press the second trigger telescopic point 382 back, thereby opening the external pump, allowing the bovine collagen peptide to be supplemented through the bovine collagen peptide input pipe 6 and the carbon dioxide through the carbon dioxide input pipe 7, and then closing the external pump.

[0059] Finally, the reaction cylinder 2 is provided with a bovine collagen peptide discharge pipe 9 at the bottom, and a carbon dioxide discharge pipe 8 at the top of the side wall. Since the reaction cylinder 2 rotates on the inner wall of the annular frame 1 through the support frame 3, the centrifugal force can effectively separate the bovine collagen peptide and carbon dioxide mixture, and the sterilized bovine collagen peptide is discharged from the bovine collagen peptide discharge pipe 9, and the carbon dioxide is discharged from the carbon dioxide discharge pipe 8 at the top of the side wall of the reaction cylinder 2.

[0060] The working principle of the present application is as follows:

[0061] S1: First, the bovine collagen peptide is pumped into the buffer box 13 through the bovine collagen peptide input pipe 6 and the rubber hose, and then this part of the bovine collagen peptide enters the mixing cylinder 11 through the communication hole 25, and the carbon dioxide is pumped into the stable aeration disc 23 through the carbon dioxide input pipe 7 and the rubber hose, and then the carbon dioxide in the stable aeration disc 23 enters the aeration hole 16 through the air inlet hole 17 on the rotating shaft 5, and then reaches the mixing cylinder 11, thus completing the function of introducing bovine collagen peptide and carbon dioxide into the mixing cylinder 11;

[0062] S2: Then, the external driving mechanism is opened to drive the rotating rod 4 to rotate, since the driving mechanism 10 is arranged on the rotating rod 4, and the driving mechanism 10 is connected with the reaction cylinder 2 through the rotating shaft 5, when the rotating rod 4 rotates, it can drive the reaction cylinder 2 to rotate on the inner wall of the annular frame 1 through the support frame 3, thus driving the plurality of reaction cylinders 2 to rotate around the rotating rod 4, and the driving motor built in the driving mechanism 10 drives the rotating rod 4 to rotate, and then the rotating force is transmitted to the mixing cylinder 11 in the reaction cylinder 2;

[0063] S3: the rotating rotating shaft 5 rotates with the spiral body 14, the first sparse hole 30 and the second sparse hole 31 are not in communication state and the second electromagnetic generator 36 opens the attraction to the limiting plug 34 to make the end cover 12 block the mixing cylinder 11, so that the bovine collagen peptide and carbon dioxide entering the mixing cylinder 11 are preliminarily mixed and stirred, and the bovine collagen peptide and carbon dioxide mixture in the compression cavity 20 is extruded by the piston 18 pushed by the rectangular rigid plug 33 due to the rotation of the spiral body 14, so as to realize that the carbon dioxide is dissolved in water to generate carbonic acid under high pressure and reduce the pH value, then the rectangular rigid plug 33 is pushed away from the end of the spiral body 14, and the piston 18 cannot extrude the compression cavity 20, then the rectangular rigid plug 33 is separated from the end of the spiral body 14 in the process of the spiral body 14 continuing to rotate, and the piston 18 moves reversely under the action of the first return spring 19, so that the compression cavity 20 is not compressed, and then the rectangular rigid plug 33 abuts against the outer side wall of the spiral body 14, that is, the bovine collagen peptide and carbon dioxide in the stirring cavity 21 are continuously mixed and stirred, and the bovine collagen peptide and carbon dioxide mixture in the compression cavity 20 is continuously pressurized and released under the rotation of the rotating shaft 5 with the spiral body 14;

[0064] S4: the first trigger telescopic point 381 is protruded through the electric control system, at this time the spiral body 14 carrying the end plate 15 is pressed back against the first trigger telescopic point 381 after passing the second trigger telescopic point 382 which is not protruded, at this time the second trigger telescopic point 382 is protruded, and the piston 18 compresses the compression cavity 20 to the state that it cannot continue to compress;

[0065] S5: then the electric control system closes the second electromagnetic generator 36, so that the end cover 12 no longer blocks the mixing cylinder 11, at this time the compression cavity 20 under high pressure is rapidly released, the bovine collagen peptide and carbon dioxide mixture in the compression cavity 20 is released, the carbon dioxide is dissolved in water to generate carbonic acid under high pressure, the pH value is reduced, then it penetrates into the microbial cells and rapidly reduces the pressure, which causes the cells to rupture and produce a blasting effect, so as to kill bacteria, yeast and mold, then the second electromagnetic generator 36 is reopened, and the end cover 12 repeatedly blocks the end of the mixing cylinder 11;

[0066] S6: Re-start the electromagnetic pump to make the first and second material holes 30 and 31 communicate, and at the same time, start the first electromagnetic generator 27 to generate the same magnetic field as the second magnet plate on the blocking ring 26, which pushes the blocking ring 26 to block the communication hole 25. Under the action of the first return spring 19, the piston 18 moves reversely, so that the mixture of bovine collagen peptide and carbon dioxide originally existing in the stirring cavity 21 is squeezed into the compression cavity 20 through the first and second material holes 30 and 31. When the rectangular rigid rod 33 re-touches the outer wall of the spiral body 14, the electromagnetic pump is closed to block the flow channel of the first and second material holes 30 and 31, and the first electromagnetic generator 27 is closed. The end magnetic block 29 pushes the blocking ring 26 with the second magnet plate to expose the communication hole 25, which is convenient for subsequent material supplementing;

[0067] S7: Then, during the rotation of the spiral body 14 for one circle, the spiral body 14 with the end plate 15 will first touch the protruding second trigger extension point 382, and then press the second trigger extension point 382 to retract, thereby opening the external pump to supplement the bovine collagen peptide through the bovine collagen peptide input pipe 6 and the carbon dioxide through the carbon dioxide input pipe 7. Subsequently, the external pump is closed. Finally, since the reaction cylinder 2 rotates on the inner wall of the annular frame 1 through the support frame 3, the bovine collagen peptide and carbon dioxide mixture can be effectively separated by centrifugal force. The sterilized bovine collagen peptide is discharged from the bovine collagen peptide discharge pipe 9, and the carbon dioxide is discharged from the carbon dioxide discharge pipe 8 on the top of the side wall of the reaction cylinder 2.

[0068] The above is only the preferred specific embodiment of the present application, but the protection scope of the present application is not limited thereto. Any person skilled in the art can make equivalent replacement or change according to the technical solution and the inventive concept of the present application within the technical range disclosed by the present application, which should be covered within the protection scope of the present application.

Claims

1. A device for rapid sterilization of bovine collagen peptide, comprising two annular frames and a rotating rod coaxially arranged with the annular frames, the two annular frames are coaxially arranged in an upper and lower manner, characterized in that, A plurality of reaction cylinders are coaxially arranged in the annular frame, and the plurality of reaction cylinders are circumferentially arranged. The reaction cylinders rotate on the inner wall of the annular frame through the support frame. The reaction cylinders are provided with a bovine collagen peptide input pipe and a carbon dioxide input pipe for feeding bovine collagen peptide and carbon dioxide into the mixing cylinder. A plurality of mixing cylinders are linearly fixed in the reaction cylinder through the cylinder support. The inner wall of the mixing cylinder is fixed with a limiting frame. A rectangular rigid insertion rod sliding on the limiting frame is fixed on the piston. The rectangular rigid insertion rod abuts against the spiral body. The spiral body is oriented towards the piston. The piston is connected with the end cover through the first return spring. A plurality of rotating shafts are coaxially inserted into the reaction cylinder on the rotating rod. The rotating shafts are inserted into the mixing cylinder. The mixing cylinder is slidably provided with a piston for separating the mixing cylinder into a compression cavity and an agitation cavity. The outer side wall of the rotating shaft is provided with a spiral body located in the agitation cavity. The spiral body drives the piston to extrude the bovine collagen peptide and carbon dioxide mixture in the compression cavity. The compression cavity of the mixing cylinder is provided with an end cover movably arranged and discharging bovine collagen peptide. The inner wall of the mixing cylinder is provided with a first material dispersing hole and a second material dispersing hole in communication with each other. The first material dispersing hole and the second material dispersing hole are located on both sides of the piston. The first material dispersing hole is provided with an electromagnetic pump.

2. The rapid sterilization device for bovine collagen peptide according to claim 1, characterized in that, A plurality of driving mechanisms are arranged on the rotating rod along the shaft. The driving mechanism includes a plurality of driving motors. The driving motors are one-to-one corresponding to the reaction cylinders. The output end of the driving motor is coaxially fixed with the rotating shaft.

3. The device for rapid sterilization of bovine collagen peptides according to claim 2, characterized in that, The end cover coaxially slides on the end of the mixing cylinder through the sliding groove and the limiting insertion rod. The sliding groove is arranged on the end of the mixing cylinder. The second electromagnetic generator is arranged in the sliding groove. The limiting insertion rod is reset and retracted in the sliding groove through the second return spring. The limiting insertion rod is provided with a first magnet plate towards the side of the second electromagnetic generator.

4. The device for rapid sterilization of bovine collagen peptides according to claim 3, characterized in that, A stable aeration disc is coaxially fixed on the mixing cylinder. A second communication pipe is inserted into the stable aeration disc. An aeration hole is arranged on the rotating shaft in communication with the agitation cavity. The stable aeration disc is in communication with the aeration hole through the air inlet hole.

5. The device for rapid sterilization of bovine collagen peptides according to claim 4, characterized in that, A buffer tank is arranged on the outer side wall of the mixing cylinder. The buffer tank is in communication with the mixing cylinder through the communication hole. The buffer tank is an elastic tank. A blocking ring is slidably arranged on the outer side wall of the mixing cylinder for blocking the communication hole. A first electromagnetic generator is fixed in the buffer tank. The blocking ring slides through the limiting rod fixed on the first electromagnetic generator. An end magnetic block is arranged on the sliding end of the limiting rod. A second magnet plate is arranged on the side of the blocking ring towards the first electromagnetic generator. A first communication pipe is arranged on the buffer tank.

6. The device for rapid sterilization of bovine collagen peptides according to claim 5, characterized in that, The bovine collagen peptide input pipe is in communication with the first communication pipe through a rubber hose. The carbon dioxide input pipe is in communication with the second communication pipe through a rubber hose. A bovine collagen peptide discharge pipe is arranged at the bottom of the reaction cylinder. A carbon dioxide discharge pipe is arranged at the top of the side wall of the reaction cylinder.

7. The device for rapid sterilization of bovine collagen peptides according to claim 6, characterized in that, An end plate abutting against the inner wall of the end of the mixing cylinder is fixed on the side of the stable aeration disc towards the spiral body. A trigger part is arranged on the inner wall of the end of the mixing cylinder. The trigger part includes a first trigger expansion point and a second trigger expansion point. The end of the first trigger expansion point and the second trigger expansion point is provided with a rounded corner. The trigger part is connected with the first electromagnetic generator, the second electromagnetic generator and the electromagnetic pump through an electric control system.

8. A sterilization method of a rapid sterilization device for bovine collagen peptide, applied to the rapid sterilization device for bovine collagen peptide of claim 7, characterized in that, The specific operation steps are as follows: S1: First, the bovine collagen peptide is pumped into the buffer box through the bovine collagen peptide input pipe and the rubber hose, and then the bovine collagen peptide enters the mixing cylinder through the communication hole, and the carbon dioxide is pumped into the stable aeration disc through the carbon dioxide input pipe and the rubber hose, which completes the function of introducing bovine collagen peptide and carbon dioxide into the mixing cylinder; S2: Then drive the rotating rod to rotate, which can drive the reaction cylinder to rotate in the inner wall of the annular frame through the support frame, and the built-in drive motor of the driving mechanism drives the rotating rod to rotate, and the rotating force is transmitted to the mixing cylinder in the reaction cylinder; S3: The rotating shaft rotates with the spiral body, and the bovine collagen peptide and carbon dioxide are preliminarily mixed and stirred, the piston extrudes the bovine collagen peptide and carbon dioxide mixture in the compression cavity, and then realizes that carbon dioxide dissolves in water to generate carbonic acid under high pressure and reduces the pH value; S4: The first trigger expansion point is protruded by the electric control system, and the spiral body with the end plate presses the second trigger expansion point which is not protruded and is pressed back against the first trigger expansion point, and the second trigger expansion point is protruded at this time, and the piston compresses the compression cavity to the state that it cannot continue to compress; S5: Then the electric control system closes the second electromagnetic generator, releases the bovine collagen peptide and carbon dioxide mixture in the compression cavity, and then penetrates into the microbial cells and rapidly reduces the pressure, which causes the cells to rupture and produce a blasting effect, thereby killing bacteria, yeast and mold; S6: Then open the electromagnetic pump to connect the first and second material discharge holes, and extrude the bovine collagen peptide and carbon dioxide mixture originally in the stirring cavity into the compression cavity through the first and second material discharge holes; S7: Then the second trigger expansion point is pressed back, and then the external pump is opened, the bovine collagen peptide is supplemented through the bovine collagen peptide input pipe, and the carbon dioxide is supplemented through the carbon dioxide input pipe, the bovine collagen peptide after sterilization is discharged from the bovine collagen peptide discharge pipe, and the carbon dioxide is discharged from the carbon dioxide discharge pipe at the top of the reaction cylinder side wall.

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