Rapid sterilization device and sterilization method for bovine bone collagen peptide

Abstract

The invention relates to the technical field of sterilization, and discloses a bovine bone collagen peptide rapid sterilization device and a sterilization method.The bovine bone collagen peptide rapid sterilization device comprises two annular frames and a rotating rod coaxially arranged with the annular frames, the two annular frames are coaxially arranged up and down, a plurality of reaction cylinders are coaxially arranged in the annular frames, and the reaction cylinders rotate on the inner walls of the annular frames through supporting frames; and the reaction cylinder is provided with a bovine bone collagen peptide input pipe and a carbon dioxide input pipe which are used for introducing bovine bone collagen peptide and carbon dioxide into the mixing cylinder. The electric control system closes the second electromagnetic generator, the end cover does not block the mixing cylinder any more, at the moment, the compression cavity in high pressure can be rapidly released, a mixture of bovine bone collagen peptide and carbon dioxide in the compression cavity is released, carbon dioxide is dissolved in water under high pressure to generate carbonic acid, the pH value is reduced, and the energy consumption is reduced. Then, after penetrating into microbial cells, the pressure is quickly reduced, so that the cells are broken to generate a blasting effect, and bacteria, yeasts and moulds are killed.

Description

Technical Field

[0001] The present invention relates to the field of sterilization technology, in particular to a bovine collagen peptide rapid sterilization device and a sterilization method. Background Art

[0002] Bovine collagen peptides are sensitive to heat. Traditional heat sterilization methods (such as high-temperature instantaneous sterilization) can easily cause denaturation, inactivation, Maillard reaction, and unpleasant flavors. Therefore, they need to have the following characteristics: low temperature resistance: the entire process is carried out at low temperature or instantaneous medium temperature, usually less than 65°C, to prevent collagen peptide denaturation. Therefore, conventional heating sterilization methods are not suitable for the sterilization of bovine collagen peptides. Therefore, non-heating sterilization methods are usually used for the sterilization of bovine collagen peptides. However, the above sterilization methods will have the following problems: First, in order to avoid the inactivation of bovine collagen peptides due to high temperature, ultraviolet lamps are used to kill the microbial cells in the bovine collagen peptides. Secondly, this direct use of ultraviolet disinfection usually cannot achieve full coverage of the bovine collagen peptides, so it is necessary to constantly stir to disinfect areas that are not exposed to ultraviolet rays, which will undoubtedly reduce the disinfection efficiency.

[0003] To this end, we designed a rapid sterilization device and method for bovine collagen peptide. Summary of the Invention

[0004] The purpose of the present invention is to solve the problem of inactivation of bovine collagen peptides due to high temperature in the prior art, and to propose a bovine collagen peptide rapid sterilization device and sterilization method.

[0005] In order to achieve the above object, the present invention adopts the following technical solutions: A bovine collagen peptide rapid sterilization device comprises two annular frames and a rotating rod coaxially arranged with the annular frames. The two annular frames are coaxially arranged up and down, and a plurality of reaction cylinders are coaxially arranged inside the annular frames. The plurality of reaction cylinders are arranged in a circle. The reaction cylinders rotate on the inner wall of the annular frames via a support frame. The reaction cylinders are provided with a bovine collagen peptide input tube and a carbon dioxide input tube for passing bovine collagen peptide and carbon dioxide into a mixing cylinder. The reaction cylinders are provided with a plurality of mixing cylinders, and the plurality of mixing cylinders are linearly fixed in the reaction cylinder via a cylinder bracket. The rotating rod is provided with multiple rotating shafts coaxially inserted into the reaction cylinder, and the rotating shafts are inserted into the mixing cylinder. A piston slides in the mixing cylinder and is used to separate the mixing cylinder into a compression chamber and a stirring chamber. The outer wall of the rotating shaft is provided with a spiral located in the stirring chamber. The spiral drives the piston to squeeze the bovine collagen peptide and carbon dioxide mixture in the compression chamber. An end cap is movably provided at one end of the mixing cylinder to discharge the bovine collagen peptide.

[0006] Preferably, a plurality of driving mechanisms are provided along the axis of the rotating rod, and the driving mechanisms include 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.

[0007] Preferably, a limit frame is fixed on the inner wall of the mixing cylinder, and a rectangular rigid plug is fixed on the piston to slide on the limit frame. The rectangular rigid plug is against the spiral body, and the spiral body rotates toward the piston. The piston is connected to the end cover through a first return spring.

[0008] Preferably, the end cover slides coaxially at the end of the mixing barrel through a sliding groove and a limiting rod. The sliding groove is opened at the end of the mixing barrel, and a second electromagnetic generator is provided in the sliding groove. The limiting rod is reset and retracted in the sliding groove by a second reset spring, and a first magnet plate is provided on the side of the limiting rod facing the second electromagnetic generator.

[0009] Preferably, a first material discharge hole and a second material discharge hole that are interconnected are opened on the inner wall of the mixing cylinder, and the first material discharge hole and the second material discharge hole are located on both sides of the piston, and an electromagnetic pump is arranged in the first material discharge hole.

[0010] Preferably, a stable vent disc is coaxially fixed on the mixing cylinder, and a second connecting pipe is inserted into the stable vent disc. A vent hole connected to the stirring chamber is opened on the rotating shaft, and the stable vent disc is connected to the vent hole through the air inlet hole.

[0011] Preferably, a buffer box is provided on the outer wall of the mixing cylinder, and the buffer box is connected to the mixing cylinder through a connecting hole. The buffer box is an elastic box, and a retaining ring is sliding on the outer wall of the mixing cylinder for blocking the connecting hole. A first electromagnetic generator is also fixed in the buffer box, and the retaining ring slides through a limit rod fixed on the first electromagnetic generator, and an end magnetic block is provided at the sliding end of the limit rod. A second magnet plate is provided on the side of the retaining ring facing the first electromagnetic generator, and a first connecting pipe is provided on the buffer box.

[0012] Preferably, the bovine collagen peptide input pipe is connected to the first connecting pipe through a rubber hose, the carbon dioxide input pipe is connected to the second connecting pipe through a rubber hose, a bovine collagen peptide discharge pipe is provided at the bottom of the reaction cylinder, and a carbon dioxide discharge pipe is provided at the top of the side wall of the reaction cylinder.

[0013] Preferably, an end plate is fixed on the side of the spiral body facing the stable ventilation disk, and the inner wall of the end of the mixing barrel is abutted. The inner wall of the end of the mixing barrel is provided with a trigger part, which includes a first trigger telescopic point and a second trigger telescopic point. The ends of the first trigger telescopic point and the second trigger telescopic point are both provided with rounded corners. The trigger part is connected to the first electromagnetic generator, the second electromagnetic generator and the electromagnetic pump through an electronic control system.

[0014] A sterilization method for a bovine collagen peptide rapid sterilization device, the specific operating steps are as follows: S1: First, the bovine collagen peptide is pumped into the buffer tank through the bovine collagen peptide input tube and the rubber hose. Then, this part of the bovine collagen peptide enters the mixing cylinder through the connecting hole, while the carbon dioxide is pumped into the stable ventilation plate through the carbon dioxide input tube and the rubber hose, completing the function of introducing the bovine collagen peptide and carbon dioxide into the mixing cylinder. S2: Then the rotating rod is driven to rotate. When the rotating rod rotates, it can drive the reaction cylinder to rotate on the inner wall of the annular frame through the support frame. At the same time, the driving motor built into the driving mechanism drives the rotating rod to rotate. This part of the rotational force is transmitted to the mixing cylinder located in the reaction cylinder; S3: The rotating shaft rotates with the spiral body, and the bovine collagen peptide and carbon dioxide are initially mixed and stirred. The piston squeezes the bovine collagen peptide and carbon dioxide mixture in the compression chamber, thereby achieving the dissolution of carbon dioxide in water under high pressure to generate carbonic acid and reduce the pH value; S4: The first trigger telescopic point is protruded by the electronic control system. At this time, the spiral body carrying the end plate passes over the second trigger telescopic point that is not protruded, and presses against the first trigger telescopic point to compress it back. At this time, the second trigger telescopic point is protruded, and the piston compresses the compression chamber to a state where it can no longer compress. S5: The electronic control system then turns off the second electromagnetic generator, releasing the bovine collagen peptide and carbon dioxide mixture in the compression chamber. The mixture then penetrates into the microbial cells and rapidly decompresses, causing the cells to rupture and produce an explosive effect, thereby killing bacteria, yeast, and mold. S6: Turn on the electromagnetic pump again to connect the first material-discharging hole with the second material-discharging hole, and squeeze the bovine collagen peptide and carbon dioxide mixture originally in the stirring chamber into the compression chamber through the first material-discharging hole and the second material-discharging hole; S7: Then the second trigger telescopic point is pressed and retracted, and the external pump is turned on to allow the bovine collagen peptide to pass through the bovine collagen peptide input tube and the carbon dioxide to be fed through the carbon dioxide input tube. The sterilized bovine collagen peptide will be discharged from the bovine collagen peptide discharge tube, and the carbon dioxide will be discharged from the carbon dioxide discharge tube on the top of the side wall of the reaction cylinder.

[0015] The beneficial effects of the present invention are: 1. In the present invention, as the spiral body continues to rotate, the rectangular rigid rod will detach from the end of the spiral body. Under the action of the first return spring, the piston moves in the opposite direction and no longer compresses the compression chamber. Then the rectangular rigid rod will press against the outer wall of the spiral body again, that is, as the rotating shaft rotates with the spiral body, the bovine bone collagen peptide and carbon dioxide in the stirring chamber can be continuously mixed and stirred, and the bovine bone collagen peptide and carbon dioxide mixture in the compression chamber can be continuously pressurized and released.

[0016] 2. In the present invention, the electronic control system turns off the second electromagnetic generator so that the end cover no longer blocks the mixing barrel. At this time, the high-pressure compression chamber will be quickly released, releasing the bovine collagen peptide and carbon dioxide mixture in the compression chamber. Carbon dioxide dissolves in water under high pressure to generate carbonic acid, lowering the pH value, and then penetrates into the microbial cells and quickly reduces the pressure, causing the cells to rupture and produce an explosive effect, thereby killing bacteria, yeast and mold. BRIEF DESCRIPTION OF THE DRAWINGS

[0017] Figure 1 This is a schematic structural diagram of a bovine collagen peptide rapid sterilization device proposed by the present invention; Figure 2 This is a schematic structural diagram of a reaction tube in a bovine collagen peptide rapid sterilization device proposed by the present invention; Figure 3 This is a main cross-sectional view of a reaction cylinder in a bovine collagen peptide rapid sterilization device proposed by the present invention; Figure 4 This is a schematic structural diagram of the first state of a mixing barrel in a bovine collagen peptide rapid sterilization device proposed by the present invention; Figure 5 for Figure 4 A schematic diagram of the structure at center A; Figure 6 The left and right isometric views of a mixing barrel in a bovine collagen peptide rapid sterilization device proposed in the present invention; Figure 7 This is a main cross-sectional view of a mixing barrel in a bovine collagen peptide rapid sterilization device proposed by the present invention in a first state; Figure 8 for Figure 7 A magnified schematic diagram of the structure at B in the middle; Figure 9 This is a schematic diagram of the structure of the spirochete in a bovine collagen peptide rapid sterilization device proposed by the present invention; Figure 10 This is a schematic structural diagram of the second state of the mixing barrel in the bovine collagen peptide rapid sterilization device proposed by the present invention; Figure 11 This is a main cross-sectional view of the mixing barrel in the second state of a bovine collagen peptide rapid sterilization device proposed by the present invention; Figure 12 This is a schematic structural diagram of the triggering part of a bovine collagen peptide rapid sterilization device proposed by the present invention.

[0018] In the figure: 1. Ring frame; 2. Reaction cylinder; 3. Support frame; 4. Rotating rod; 5. Rotating shaft; 6. Bovine collagen peptide inlet tube; 7. Carbon dioxide inlet tube; 8. Carbon dioxide outlet tube; 9. Bovine collagen peptide outlet tube; 10. Driving mechanism; 11. Mixing cylinder; 12. End cover; 13. Buffer box; 14. Helix; 15. End plate; 16. Vent hole; 17. Air inlet hole; 18. Piston; 19. First return spring 20. Compression chamber; 21. Stirring chamber; 22. First connecting pipe; 23. Stable vent plate; 24. Second connecting pipe; 25. Connecting hole; 26. Retaining ring; 27. First electromagnetic generator; 28. Limit rod; 29. ​​End magnetic block; 30. First material discharging hole; 31. Second material discharging hole; 32. Limiting frame; 33. Rectangular rigid plug rod; 34. Limiting plug rod; 35. Sliding groove; 36. Second electromagnetic generator; 37. Second return spring; 38. Trigger part; 381. First trigger telescopic point; 382. Second trigger telescopic point. DETAILED DESCRIPTION

[0019] Reference Figures 1-12 A bovine collagen peptide rapid sterilization device includes two annular frames 1 and a rotating rod 4 coaxially arranged with the annular frames 1. The two annular frames 1 are coaxially arranged up and down. Multiple reaction cylinders 2 are coaxially arranged inside the annular frames 1. The multiple reaction cylinders 2 are arranged in a circle. The reaction cylinders 2 rotate on the inner wall of the annular frames 1 through the support frame 3, providing driving force for the rotation of the reaction cylinders 2.

[0020] The reaction cylinder 2 is provided with a bovine collagen peptide input tube 6 and a carbon dioxide input tube 7 for passing bovine collagen peptide and carbon dioxide into a mixing cylinder 11. A plurality of mixing cylinders 11 are provided in the reaction cylinder 2, and the plurality of mixing cylinders 11 are linearly fixed in the reaction cylinder 2 by a cylinder bracket.

[0021] The bovine collagen peptide is pumped into the buffer tank 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 barrel 11 through the connecting hole 25. A stable vent disc 23 is coaxially fixed on the mixing barrel 11, and a second connecting pipe 24 is inserted on the stable vent disc 23. The bovine collagen peptide input pipe 6 is connected to the first connecting pipe 22 through the rubber hose, and the carbon dioxide input pipe 7 is connected to the second connecting pipe 24 through the rubber hose. A vent hole 16 connected to the stirring chamber 21 is provided on the rotating shaft 5, and the stable vent disc 23 is connected to the vent hole 16 through the air inlet 17. The carbon dioxide is pumped into the stable vent disc 23 through the carbon dioxide input pipe 7 and the rubber hose, and then the carbon dioxide in the stable vent disc 23 enters the vent hole 16 through the air inlet 17 on the rotating shaft 5, and then reaches the mixing barrel 11, thereby completing the effect of introducing bovine collagen peptide and carbon dioxide into the mixing barrel 11.

[0022] A plurality of drive mechanisms 10 are provided along the axis of the rotating rod 4. The drive mechanisms 10 include a plurality of drive motors. The drive motors correspond one to one with the reaction cylinders 2. The output ends of the drive motors are coaxially fixed with the rotating shaft 5. By turning on the external drive mechanism, the rotating rod 4 is driven to rotate. Since the drive mechanism 10 is provided on the rotating rod 4 and the drive mechanism 10 is connected to the reaction cylinder 2 through the rotating shaft 5, when the rotating rod 4 rotates, the reaction cylinder 2 can be driven to rotate on the inner wall of the annular frame 1 through the support frame 3.

[0023] Therefore, the multiple reaction cylinders 2 are driven to rotate around the rotating rod 4 , and the driving motor built into the driving mechanism 10 drives the rotating rod 4 to rotate, and then this part of the rotational force is transmitted to the mixing cylinder 11 located in the reaction cylinder 2 .

[0024] The rotating rod 4 is provided with multiple rotating shafts 5 coaxially inserted into the reaction cylinder 2, and the rotating shafts 5 are inserted into the mixing cylinder 11. The rotating rotating shafts 5 rotate together with the spiral 14. The outer wall of the rotating shaft 5 is provided with the spiral 14 located in the stirring chamber 21. The spiral 14 drives the piston 18 to squeeze the bovine collagen peptide and carbon dioxide mixture located in the compression chamber 20.

[0025] A piston 18 slides inside the mixing cylinder 11 and is used to separate the mixing cylinder 11 into a compression chamber 20 and a stirring chamber 21. A first material discharge hole 30 and a second material discharge hole 31 that are interconnected are opened on the inner wall of the mixing cylinder 11, and the first material discharge hole 30 and the second material discharge hole 31 are located on both sides of the piston 18. An electromagnetic pump is provided in the first material discharge hole 30.

[0026] One end of the mixing barrel 11 is provided with an end cap 12 for movably discharging the bovine collagen peptide. The end cap 12 slides coaxially at the end of the mixing barrel 11 through a sliding groove 35 and a limiting rod 34. The sliding groove 35 is provided at the end of the mixing barrel 11, and a second electromagnetic generator 36 is provided in the sliding groove 35. The limiting rod 34 is reset and retracted in the sliding groove 35 by a second reset spring 37. A first magnet plate is provided on the side of the limiting rod 34 facing the second electromagnetic generator 36. The first discharge hole 30 and the second discharge hole 31 are not in a connected state, and the second electromagnetic generator 36 starts to attract the limiting plug 34 to allow the end cover 12 to block the mixing barrel 11. Therefore, the bovine collagen peptide and carbon dioxide entering the mixing barrel 11 are preliminarily mixed and stirred. Due to the rotation of the spiral body 14, the piston 18 can be pushed by the rectangular rigid plug 33 to squeeze the bovine collagen peptide and carbon dioxide mixture in the compression chamber 20, thereby realizing that the carbon dioxide dissolves in water under high pressure to generate carbonic acid and reduce the pH value.

[0027] A limit frame 32 is fixed to the inner wall of the mixing cylinder 11, and a rectangular rigid plug rod 33 sliding on the limit frame 32 is fixed to the piston 18. The rectangular rigid plug rod 33 is in contact with the spiral body 14, and the rotation direction of the spiral body 14 is toward the piston 18. The piston 18 is connected to the end cover 12 through the first return spring 19. Since the rectangular rigid plug rod 33 is in contact with the outer wall of the spiral body 14, when the rectangular rigid plug rod 33 is pushed away to the end of the spiral body 14, the piston 18 can no longer squeeze the compression chamber 20.

[0028] Then, as the spiral body 14 continues to rotate, the rectangular rigid rod 33 will separate from the end of the spiral body 14. Under the action of the first return spring 19, the piston 18 moves in the opposite direction and no longer compresses the compression chamber 20. Then, the rectangular rigid rod 33 rests against the outer wall of the spiral body 14 again, that is, as the rotating shaft 5 rotates with the spiral body 14, the bovine bone collagen peptide and carbon dioxide in the stirring chamber 21 can be continuously mixed and stirred, and the bovine bone collagen peptide and carbon dioxide mixture in the compression chamber 20 can be continuously pressurized and released.

[0029] An end plate 15 is fixed to the side of the spiral body 14 facing the stable ventilation disk 23, which is against the inner wall of the end of the mixing cylinder 11. A trigger part 38 is provided on the inner wall of the end of the mixing cylinder 11. 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 rounded corners. The trigger part 38 is connected to the first electromagnetic generator 27, the second electromagnetic generator 36 and the electromagnetic pump through the electronic control system. The first trigger telescopic point 381 is protruded by the electronic control system. At this time, the spiral body 14 carrying the end plate 15 passes over the second trigger telescopic point 382 that has not protruded, and is pressed back against the first trigger telescopic point 381. At this time, the second trigger telescopic point 382 protrudes, and the piston 18 compresses the compression chamber 20 to a state where it can no longer be compressed.

[0030] The electronic control system then turns off the second electromagnetic generator 36, so that the end cover 12 no longer blocks the mixing barrel 11. At this time, the high-pressure compression chamber 20 will be quickly released, releasing the bovine collagen peptide and carbon dioxide mixture in the compression chamber 20. The carbon dioxide dissolves in water under high pressure to generate carbonic acid, thereby lowering the pH value.

[0031] Then, after penetrating into the microbial cells, the pressure is rapidly reduced, causing the cells to rupture and produce an explosion effect, thereby killing bacteria, yeast and mold. Then, the second electromagnetic generator 36 is turned on again, and the end cover 12 will re-seal the end of the mixing cylinder 11.

[0032] A buffer box 13 is provided on the outer wall of the mixing drum 11. The buffer box 13 is connected to the mixing drum 11 through a connecting hole 25. The buffer box 13 is an elastic box. A first connecting pipe 22 is provided on the buffer box 13. A retaining ring 26 for blocking the connecting hole 25 is sliding on the outer wall of the mixing drum 11. A first electromagnetic generator 27 is also fixed in the buffer box 13. The retaining ring 26 slides through a limit rod 28 fixed on the first electromagnetic generator 27, and an end magnetic block 29 is provided at the sliding end of the limit rod 28. A second magnet plate is provided on the side of the retaining ring 26 facing the first electromagnetic generator 27.

[0033] Turn on the electromagnetic pump to connect the first material discharge hole 30 and the second material discharge hole 31, and at the same time turn on the first electromagnetic generator 27 to generate the same magnetic field as the second magnet plate on the baffle ring 26, push the baffle ring 26 to block the connecting hole 25, and under the action of the first return spring 19, the piston 18 moves in the opposite direction, thereby squeezing the bovine collagen peptide and carbon dioxide mixture originally in the stirring chamber 21 into the compression chamber 20 through the first material discharge hole 30 and the second material discharge hole 31. When the rectangular rigid insertion rod 33 is pressed against the outer wall of the spiral body 14 again, the electromagnetic pump is turned off to block the flow channels of the first material discharge hole 30 and the second material discharge hole 31, and the first electromagnetic generator 27 is turned off at the same time. The end magnetic block 29 pushes the baffle ring 26 with the second magnet plate to expose the connecting hole 25, which is convenient for subsequent feeding.

[0034] Then, as the spiral 14 rotates one circle, the spiral 14 with the end plate 15 will first touch the protruding second trigger telescopic point 382, ​​and then press the second trigger telescopic point 382 to retract, thereby turning on the external pump, allowing the bovine collagen peptide to be fed through the bovine collagen peptide input tube 6 and the carbon dioxide to be fed through the carbon dioxide input tube 7, and then the external pump is turned off.

[0035] Finally, a bovine collagen peptide discharge pipe 9 is provided at the bottom of the reaction cylinder 2, and a carbon dioxide discharge pipe 8 is provided at the top of the side wall of the reaction cylinder 2. 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 the carbon dioxide mixture can be effectively separated by centrifugal force. The sterilized bovine collagen peptide will be discharged from the bovine collagen peptide discharge pipe 9, and the carbon dioxide will be discharged from the carbon dioxide discharge pipe 8 at the top of the side wall of the reaction cylinder 2.

[0036] The working principle of the present invention is as follows: S1: First, the bovine collagen peptide is pumped into the buffer tank 13 through the bovine collagen peptide input pipe 6 and the rubber hose. Then, this part of the bovine collagen peptide enters the mixing barrel 11 through the connecting hole 25, and the carbon dioxide is pumped into the stable vent disk 23 through the carbon dioxide input pipe 7 and the rubber hose. Then, the carbon dioxide in the stable vent disk 23 enters the vent hole 16 through the air inlet hole 17 on the rotating shaft 5, and then reaches the mixing barrel 11, thereby completing the effect of introducing the bovine collagen peptide and carbon dioxide into the mixing barrel 11; S2: Then, the external driving mechanism is turned on to drive the rotating rod 4 to rotate. Since the driving mechanism 10 is provided on the rotating rod 4 and is connected to the reaction cylinder 2 via 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 via the support frame 3, thereby driving multiple reaction cylinders 2 to rotate around the rotating rod 4. At the same time, the driving motor built into the driving mechanism 10 drives the rotating rod 4 to rotate, and this part of the rotational force is then transmitted to the mixing cylinder 11 located in the reaction cylinder 2; S3: The rotating shaft 5 rotates with the spiral body 14, the first material discharging hole 30 and the second material discharging hole 31 are not in a connected state, and the second electromagnetic generator 36 starts to attract the limiting plug 34 to allow the end cover 12 to block the mixing barrel 11, so that the bovine collagen peptide and carbon dioxide entering the mixing barrel 11 are preliminarily mixed and stirred. Due to the rotation of the spiral body 14, the piston 18 can be pushed by the rectangular rigid plug 33 to squeeze the bovine collagen peptide and carbon dioxide mixture in the compression chamber 20, thereby realizing that carbon dioxide dissolves in water under high pressure to generate carbonic acid and reduce the pH value. Then, due to the rectangular rigid plug 33 and the spiral body 14 The outer walls are against each other. When the rectangular rigid rod 33 is pushed away from the end of the spiral body 14 and the piston 18 can no longer squeeze the compression chamber 20, the spiral body 14 continues to rotate. The rectangular rigid rod 33 will be separated from the end of the spiral body 14. Under the action of the first return spring 19, the piston 18 moves in the opposite direction and no longer compresses the compression chamber 20. Then the rectangular rigid rod 33 is pressed against the outer wall of the spiral body 14 again. That is, as the rotating shaft 5 rotates with the spiral body 14, the bovine bone collagen peptide and carbon dioxide in the stirring chamber 21 can be continuously mixed and stirred, and the bovine bone collagen peptide and carbon dioxide mixture in the compression chamber 20 can be continuously pressurized and released. S4: The first trigger telescopic point 381 is protruded by the electronic control system. At this time, the spiral body 14 carrying the end plate 15 passes over the second trigger telescopic point 382 which is not protruded, and is pressed back against the first trigger telescopic point 381. At this time, the second trigger telescopic point 382 is protruded. At this time, the piston 18 compresses the compression chamber 20 to a state where it can no longer be compressed. S5: The electronic control system then turns off the second electromagnetic generator 36, allowing the end cap 12 to no longer block the mixing barrel 11. At this time, the high-pressure compression chamber 20 will be quickly released, releasing the bovine collagen peptide and carbon dioxide mixture in the compression chamber 20. Carbon dioxide dissolves in water under high pressure to form carbonic acid, lowering the pH value. It then penetrates into the microbial cells and quickly reduces pressure, causing the cells to rupture and produce an explosive effect, thereby killing bacteria, yeast and mold. The second electromagnetic generator 36 is then turned on again, and the end cap 12 will re-seal the end of the mixing barrel 11. S6: Turn on the electromagnetic pump again to connect the first material discharge hole 30 and the second material discharge hole 31, and turn on the first electromagnetic generator 27 at the same time to generate the same magnetic field as the second magnet plate on the baffle ring 26, pushing the baffle ring 26 to block the connecting hole 25. Under the action of the first return spring 19, the piston 18 moves in the opposite direction, thereby squeezing the bovine collagen peptide and carbon dioxide mixture originally in the stirring chamber 21 into the compression chamber 20 through the first material discharge hole 30 and the second material discharge hole 31. When the rectangular rigid insertion rod 33 again presses against the outer wall of the spiral body 14, the electromagnetic pump is turned off again to block the flow channel of the first material discharge hole 30 and the second material discharge hole 31. At the same time, the first electromagnetic generator 27 is turned off, and the end magnetic block 29 pushes the baffle ring 26 with the second magnet plate to expose the connecting hole 25, which is convenient for subsequent material replenishment. S7: Then, as the spiral 14 rotates one circle, the spiral 14 with the end plate 15 will first touch the protruding second trigger telescopic point 382, ​​and then press the second trigger telescopic point 382 to retract, thereby turning on the external pump to allow the bovine collagen peptide to be fed through the bovine collagen peptide input tube 6 and the carbon dioxide to be fed through the carbon dioxide input tube 7, and then the external pump is turned off. 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 the carbon dioxide mixture can be effectively separated by centrifugal force, and the sterilized bovine collagen peptide will be discharged from the bovine collagen peptide discharge tube 9, and the carbon dioxide will be discharged from the carbon dioxide discharge tube 8 on the top of the side wall of the reaction cylinder 2.

[0037] The above description is only a preferred specific embodiment of the present invention, but the scope of protection of the present invention is not limited thereto. Any technician familiar with the technical field, within the technical scope disclosed by the present invention, who makes equivalent replacements or changes based on the technical solution and inventive concept of the present invention, should be covered by the scope of protection of the present invention.

Claims

1. A bovine collagen peptide rapid sterilization device, comprising two annular frames and a rotating rod coaxially arranged with the annular frames, wherein the two annular frames are coaxially arranged up and down, and characterized in that: A plurality of reaction cylinders are coaxially arranged in the annular frame, and the plurality of reaction cylinders are arranged in a circular manner. The reaction cylinders rotate on the inner wall of the annular frame through a support frame. The reaction cylinders are provided with a bovine collagen peptide input tube and a carbon dioxide input tube for passing bovine collagen peptide and carbon dioxide into a mixing cylinder. The reaction cylinder is provided with a plurality of mixing cylinders, and the plurality of mixing cylinders are linearly fixed in the reaction cylinder by a cylinder bracket. The rotating rod is provided with multiple rotating shafts coaxially inserted into the reaction cylinder, and the rotating shafts are inserted into the mixing cylinder. A piston slides in the mixing cylinder and is used to separate the mixing cylinder into a compression chamber and a stirring chamber. The outer wall of the rotating shaft is provided with a spiral located in the stirring chamber. The spiral drives the piston to squeeze the bovine collagen peptide and carbon dioxide mixture in the compression chamber. An end cap is movably provided at one end of the mixing cylinder to discharge the bovine collagen peptide.

2. The bovine collagen peptide rapid sterilization device according to claim 1, characterized in that: A plurality of driving mechanisms are arranged along the axis of the rotating rod. The driving mechanisms include a plurality of driving motors. The driving motors correspond to the reaction cylinders one by one. The output ends of the driving motors are coaxially fixed with the rotating shaft.

3. The bovine collagen peptide rapid sterilization device according to claim 2, characterized in that: A limiting frame is fixed on the inner wall of the mixing cylinder, and a rectangular rigid plug is fixed on the piston, which slides on the limiting frame. The rectangular rigid plug is against the spiral body, and the spiral body rotates toward the piston. The piston is connected to the end cover through a first return spring.

4. The bovine collagen peptide rapid sterilization device according to claim 3, characterized in that: The end cover slides coaxially at the end of the mixing barrel through a sliding groove and a limiting rod. The sliding groove is opened at the end of the mixing barrel, and a second electromagnetic generator is arranged in the sliding groove. The limiting rod is reset and retracted in the sliding groove by a second reset spring. A first magnet plate is provided on the side of the limiting rod facing the second electromagnetic generator.

5. The bovine collagen peptide rapid sterilization device according to claim 4, characterized in that: The inner wall of the mixing cylinder is provided with a first material discharge hole and a second material discharge hole which are connected to each other, and the first material discharge hole and the second material discharge hole are located on both sides of the piston, and an electromagnetic pump is arranged in the first material discharge hole.

6. The bovine collagen peptide rapid sterilization device according to claim 5, characterized in that: A stable vent plate is coaxially fixed on the mixing cylinder, and a second connecting pipe is inserted on the stable vent plate. A vent hole connected to the stirring chamber is opened on the rotating shaft, and the stable vent plate is connected to the vent hole through the air inlet hole.

7. The bovine collagen peptide rapid sterilization device according to claim 6, characterized in that: A buffer box is provided on the outer wall of the mixing cylinder, and the buffer box is connected to the mixing cylinder through a connecting hole. The buffer box is an elastic box. A retaining ring is sliding on the outer wall of the mixing cylinder for blocking the connecting hole. A first electromagnetic generator is also fixed in the buffer box. The retaining ring slides through a limit rod fixed on the first electromagnetic generator, and an end magnetic block is provided at the sliding end of the limit rod. A second magnet plate is provided on the side of the retaining ring facing the first electromagnetic generator, and a first connecting pipe is provided on the buffer box.

8. The bovine collagen peptide rapid sterilization device according to claim 7, characterized in that: The bovine collagen peptide input pipe is connected to the first connecting pipe through a rubber hose, the carbon dioxide input pipe is connected to the second connecting pipe through a rubber hose, a bovine collagen peptide discharge pipe is provided at the bottom of the reaction cylinder, and a carbon dioxide discharge pipe is provided at the top of the side wall of the reaction cylinder.

9. The bovine collagen peptide rapid sterilization device according to claim 8, characterized in that: An end plate is fixed on the side of the spiral body facing the stable ventilation disk, which is in contact with the inner wall of the end of the mixing barrel. A trigger part is provided on the inner wall of the end of the mixing barrel. The trigger part includes a first trigger telescopic point and a second trigger telescopic point. The ends of the first trigger telescopic point and the second trigger telescopic point are both provided with rounded corners. The trigger part is connected to the first electromagnetic generator, the second electromagnetic generator and the electromagnetic pump through an electronic control system.

10. A sterilization method for a bovine collagen peptide rapid sterilization device, applied to the bovine collagen peptide rapid sterilization device of claim 9, characterized in that: The specific steps are as follows: S1: First, the bovine collagen peptide is pumped into the buffer tank through the bovine collagen peptide input tube and the rubber hose. Then, this part of the bovine collagen peptide enters the mixing cylinder through the connecting hole, while the carbon dioxide is pumped into the stable ventilation plate through the carbon dioxide input tube and the rubber hose, completing the function of introducing the bovine collagen peptide and carbon dioxide into the mixing cylinder. S2: Then the rotating rod is driven to rotate. When the rotating rod rotates, it can drive the reaction cylinder to rotate on the inner wall of the annular frame through the support frame. At the same time, the driving motor built into the driving mechanism drives the rotating rod to rotate. This part of the rotational force is transmitted to the mixing cylinder located in the reaction cylinder; S3: The rotating shaft rotates with the spiral body, and the bovine collagen peptide and carbon dioxide are initially mixed and stirred. The piston squeezes the bovine collagen peptide and carbon dioxide mixture in the compression chamber, thereby achieving the dissolution of carbon dioxide in water under high pressure to generate carbonic acid and reduce the pH value; S4: The first trigger telescopic point is protruded by the electronic control system. At this time, the spiral body carrying the end plate passes over the second trigger telescopic point that is not protruded, and presses against the first trigger telescopic point to compress it back. At this time, the second trigger telescopic point is protruded, and the piston compresses the compression chamber to a state where it can no longer compress. S5: The electronic control system then turns off the second electromagnetic generator, releasing the bovine collagen peptide and carbon dioxide mixture in the compression chamber. The mixture then penetrates into the microbial cells and rapidly decompresses, causing the cells to rupture and produce an explosive effect, thereby killing bacteria, yeast, and mold. S6: Turn on the electromagnetic pump again to connect the first material-discharging hole with the second material-discharging hole, and squeeze the bovine collagen peptide and carbon dioxide mixture originally in the stirring chamber into the compression chamber through the first material-discharging hole and the second material-discharging hole; S7: Then the second trigger telescopic point is pressed and retracted, and the external pump is turned on to allow the bovine collagen peptide to pass through the bovine collagen peptide input tube and the carbon dioxide to be fed through the carbon dioxide input tube. The sterilized bovine collagen peptide will be discharged from the bovine collagen peptide discharge tube, and the carbon dioxide will be discharged from the carbon dioxide discharge tube on the top of the side wall of the reaction cylinder.

Images