Solid mixing device for producing polypeptide

Abstract

The utility model discloses a solid mixing device for producing polypeptide, and relates to the technical field of polypeptide production. The stirring device comprises a mounting assembly, wherein the mounting assembly comprises a stirring frame; inclined plates are mounted on the inner side wall of the stirring frame, a vibration motor is mounted at one end of any inclined plate, and a first mounting groove is formed in one end of the stirring frame; the vibration discharging assembly comprises two vibration plates installed on the inner side wall of the stirring frame, and a connecting block is installed at one end of any vibration plate; by means of the vibration discharging assembly, particularly the two inclined plates and the springs at the lower ends of the inclined plates, the inclined plates can be continuously vibrated through kinetic energy of a vibration motor in the discharging process, so that the downward discharging speed of polypeptide accumulated at the discharging opening between the two inclined plates is increased, and the discharging efficiency is improved. And meanwhile, residual materials accumulated on the inclined plate can be cleaned.

Description

Technical Field

[0001] The utility model relates to the technical field of polypeptide production, in particular to a solid-state mixing device for producing polypeptides. Background Art

[0002] Polypeptide calcium phosphate is a mixture of biological polypeptide and calcium phosphate minerals. It can prevent soft-shelled eggs, soft feet and wing drop, rickets, reduce feather shedding and breakage, make pigeon eggs large and smooth, and eliminate single egg phenomenon. It promotes smooth and soft feathers, increases homing rate, and promotes metabolism. It can also remove free radicals, has a calming and directional effect, and eliminates tension and fatigue for racing pigeons.

[0003] Publication No. CN 217663016 U discloses a production device for polypeptide calcium phosphate, including a tank body, a driving motor 1 is fixedly installed on the top of the tank body, a stirring shaft is fixedly connected to the bottom of the driving motor 1, a feeding pipe is fixedly connected to the side of the tank body, a feeding hopper is fixedly connected to the top of the feeding pipe, a crushing roller 1 and a crushing roller 2 are movably sleeved inside the feeding hopper, and a driving motor 3 is fixedly installed on the front of the feeding hopper. The production device for polypeptide calcium phosphate, by setting a feeding hopper, uses the driving motor 3 to drive the crushing roller 1 to rotate, and then the crushing roller 1 drives the crushing roller 2 to rotate through the transmission gear, so that the crushing roller 1 and the crushing roller 2 rotate in opposite directions, and can crush the calcium phosphate minerals to avoid the agglomeration of the calcium phosphate minerals.

[0004] Although the above device can effectively crush the polypeptide during mixing and stirring to increase the mixing effect, due to its small discharge port, the polypeptide in a solid state is easily accumulated at the discharge port and does not discharge downward, resulting in slow discharge and greatly reducing production efficiency. In addition, due to the certain viscosity of the polypeptide, a part of it will remain at the bottom of the tank and cannot be unloaded.

[0005] Therefore, a new solid-state mixing device for producing polypeptides is proposed to solve the above problems. Utility Model Content

[0006] The utility model aims to provide a solid-state mixing device for producing polypeptides to solve the technical problems raised in the background technology.

[0007] In order to solve the above technical problems, the utility model is realized by the following technical solutions:

[0008] The utility model is a solid-state mixing device for producing polypeptides, comprising a mounting assembly, wherein the mounting assembly comprises a stirring frame; an inclined plate is mounted on the inner side wall of the stirring frame, a vibration motor is mounted on one end of any inclined plate, a first mounting groove is formed at one end of the stirring frame, a second mounting groove is formed at the other end of the stirring frame away from the first mounting groove, and a second clamping groove is formed in the second mounting groove;

[0009] A vibration unloading assembly, wherein the vibration unloading assembly comprises two vibration plates installed on the inner side wall of the mixing frame, a connecting block is installed at one end of any one of the vibration plates, a first limiting rod is installed at four corners of one side of the vibration plate, four second limiting rods are installed at the same end of the vibration plate, a limiting cylinder is installed at the outer end of any one of the second limiting rods, a spring is installed in any one of the limiting cylinders, and vertical plates are installed at opposite ends of the two vibration plates; sliding grooves are symmetrically opened at the inner end of any one of the vertical plates, a filter plate is installed in the sliding groove, a filter screen is installed in the filter plate, and the filter screen is installed at the lowermost end of the inner side wall of the filter plate, a second clamping block is installed at one end of the filter plate, and a handle is installed at the other end of the filter plate away from the second clamping block, and the second clamping block and the second clamping groove are embedded;

[0010] Stirring components.

[0011] Preferably, one end of the spring close to the second limiting rod is connected to one end of the second limiting rod close to the limiting cylinder.

[0012] Preferably, four brackets are installed at the four corners of one end of the mixing frame, limiting holes are opened at the four corners of one end of any inclined plate, a first connecting hole is opened at one end of the mixing frame, a first card slot is opened at one end of the mixing frame, any one of the first limiting rods is installed in the limiting hole on the inclined plate, and any one of the limiting cylinders is connected to one end of the inclined plate close to the limiting cylinder.

[0013] Preferably, a feed hole is opened at one end of the stirring frame, a feed hopper is installed at one end of the stirring frame, the end of the feed hopper close to the stirring frame is connected to the feed hole, and the diameter of the feed hole is smaller than the inner circle diameter of the feed hopper close to the stirring frame.

[0014] Preferably, the stirring assembly includes a motor, a stirring shaft is installed at one end of the motor, a bearing is installed at the other end of the stirring shaft, a stirring rod is installed on the stirring shaft, a spiral blade is installed on the stirring shaft, the motor is installed at one end of the stirring frame, and the bearing is installed on the inner wall of the stirring frame away from the other end of the motor.

[0015] Preferably, two mounting blocks are installed at one end of the stirring frame, a rotating shaft is installed between the two mounting blocks, a discharge plate is installed outside the rotating shaft, and a first clamping block is installed at one end of the inclined plate, and the first clamping block is engaged with the first clamping groove.

[0016] Compared with the prior art, the advantages of the present invention are:

[0017] The solid-state mixing device for producing polypeptides can continuously vibrate the inclined plates by means of the kinetic energy of a vibration motor during unloading, by means of a vibration discharge component, in particular two inclined plates and a spring at the lower end of the inclined plates, so that the polypeptides accumulated at the discharge port between the two inclined plates are discharged downward faster, and residual materials accumulated on the inclined plates can be cleaned at the same time; the filter plate can be used to filter the polypeptides simultaneously during unloading, and can be removed for cleaning after a certain period of use due to the movable installation; and the stirring component can use a spiral sheet to transport the solid polypeptides at one end of the stirring frame to the other end during stirring, so as to prevent the polypeptides in the stirring frame from always being kept at a certain place, thereby increasing the stirring efficiency.

[0018] Of course, any product implementing the present invention does not necessarily need to achieve all of the advantages described above at the same time. BRIEF DESCRIPTION OF THE DRAWINGS

[0019] In order to more clearly illustrate the technical solutions of the embodiments of the utility model, the drawings required for describing the embodiments are briefly introduced below. Obviously, the drawings described below are only some embodiments of the utility model. For ordinary technicians in this field, other drawings can be obtained based on these drawings without creative work.

[0020] Figure 1 This is the installation structure diagram of the utility model;

[0021] Figure 2 This is a structural diagram of the vibration unloading assembly of the utility model;

[0022] Figure 3 This is a structural diagram of the stirring assembly of the utility model;

[0023] Figure 4 It is a cross-sectional view of the installation assembly of the utility model;

[0024] Figure 5 This is a bottom view of the installation assembly of the utility model;

[0025] Figure 6 This is a structural diagram of the unloading plate of the utility model;

[0026] Figure 7 For the utility model Figure 6 Enlarged view of point A in the middle;

[0027] Figure 8 This is a structural diagram of the filter plate of the utility model;

[0028] Fig. 9 This is a structural diagram of a mixing frame of the utility model;

[0029] Fig.10 For the utility model Fig. 9 Enlarged view of point B in the middle.

[0030] In the accompanying drawings, the components represented by the reference numerals are listed as follows:

[0031] 100, vibrating discharge assembly; 110, vibrating motor; 120, vibrating plate; 130, vertical plate; 140, first limiting rod; 150, second limiting rod; 160, limiting cylinder; 180, filter plate; 181, filter screen; 183, second block; 184, handle; 190, sliding groove; 170, spring; 200, stirring assembly; 210, motor; 220, stirring shaft; 230, stirring rod; 240, Bearing; 259, spiral piece; 300, installation assembly; 310, stirring frame; 320, first installation slot; 321, second installation slot; 322, second clamping slot; 330, inclined plate; 340, bracket; 350, first connecting hole; 360, feed hole; 370, feed hopper; 380, limit hole; 390, first clamping slot; 391, first clamping block; 392, unloading plate; 393, installation block; 394, rotating shaft. DETAILED DESCRIPTION

[0032] In the following, only some exemplary embodiments are briefly described. As those skilled in the art will appreciate, the described embodiments may be modified in various ways without departing from the spirit or scope of the embodiments of the present invention. Therefore, the drawings and descriptions are considered to be exemplary and non-restrictive in nature.

[0033] In the description of the embodiments of the present invention, it should be understood that the terms "length", "vertical", "horizontal", "top", "bottom", etc. indicating the orientation or positional relationship are based on the orientation or positional relationship shown in the accompanying drawings, and are only for the convenience of describing the embodiments of the present invention and simplifying the description, rather than indicating or implying that the device or element referred to must have a specific orientation, be constructed and operated in a specific orientation, and therefore cannot be understood as a limitation on the embodiments of the present invention.

[0034] In order to better understand the purpose, structure and function of the utility model, the following is a further detailed description of a solid-state mixing device for producing polypeptides of the utility model in conjunction with the accompanying drawings.

[0035] See also Figure 1-10As shown, this embodiment is a solid-state mixing device for producing polypeptides, including a mounting assembly 300, wherein the mounting assembly 300 includes a stirring frame 310; an inclined plate 330 is mounted on the inner side wall of the stirring frame 310, and a vibration motor 110 is mounted on one end of any inclined plate 330; a first mounting groove 320 is formed at one end of the stirring frame 310, and a second mounting groove 321 is formed at the other end of the stirring frame 310 away from the first mounting groove 320, and a second clamping groove 322 is formed in the second mounting groove 321;

[0036] The vibrating unloading assembly 100 includes two vibrating plates 120 mounted on the inner side wall of the mixing frame 310, one end of any one of the vibrating plates 120 is mounted with a connecting block, four corners of one side of the vibrating plate 120 are mounted with a first limiting rod 140, and the same end of the vibrating plate 120 is mounted with four second limiting rods 150, and the outer end of any one of the second limiting rods 150 is mounted with a limiting cylinder 160, and any one of the limiting cylinders 160 is installed with a spring 170. The two vibrating plates 1 20, a vertical plate 130 is installed at one end opposite to the other; a sliding groove 190 is symmetrically opened at the inner end of any of the vertical plates, a filter plate 180 is installed in the sliding groove 190, a filter screen 181 is installed in the filter plate 180, and the filter screen 181 is installed at the lower end of the inner wall of the filter plate 180, a second clamping block 183 is installed at one end of the filter plate 180, and a handle 184 is installed on the other end of the filter plate away from the second clamping block 183, and the second clamping block 183 is engaged with the second clamping groove 322;

[0037] Stirring assembly 200.

[0038] One end of the spring 170 close to the second limiting rod 150 is connected to one end of the second limiting rod 150 close to the limiting cylinder 160 .

[0039] Four brackets 340 are installed at the four corners of one end of the mixing frame 310, and limiting holes 380 are provided at the four corners of one end of any inclined plate 330. A first connecting hole 350 is provided at one end of the mixing frame 310, and a first card slot 390 is provided at one end of the mixing frame 310. Any one of the first limiting rods 140 is installed in the limiting hole 380 on the inclined plate 330, and any one of the limiting cylinders 160 is connected to one end of the inclined plate 330 close to the limiting cylinder 160.

[0040] A feed hole 360 ​​is opened at one end of the mixing frame 310, and a feed hopper 370 is installed at one end of the mixing frame 310. The end of the feed hopper 370 close to the mixing frame 310 is connected to the feed hole 360, and the diameter of the feed hole 360 ​​is smaller than the inner circle diameter of the feed hopper 370 close to the mixing frame 310.

[0041] The stirring assembly 200 includes a motor 210, a stirring shaft 220 is installed at one end of the motor 210, a bearing 240 is installed at the other end of the stirring shaft 220, a stirring rod 230 is installed on the stirring shaft 220, and a spiral piece 259 is installed on the stirring shaft 220. The motor 210 is installed at one end of the stirring frame 310, and the bearing 240 is installed on the other end of the inner wall of the stirring frame 310 away from the motor; the stirring rod 230 is driven by the motor to rotate around the bearing 240, and the stirring rod 230 is driven to rotate when rotating to stir the solid polypeptide in the stirring frame 310, and the spiral piece 259 on the stirring shaft 220 drives the solid polypeptide in the stirring frame 310 to move to the other end, so as to achieve more uniform stirring.

[0042] Two mounting blocks 393 are installed at one end of the mixing frame 310, a rotating shaft 394 is installed between the two mounting blocks 393, a discharge plate 392 is installed outside the rotating shaft 394, and a first clamping block 391 is installed at one end of the inclined plate 330, and the first clamping block 391 is engaged with the first clamping groove 390; the discharge plate 392 is engaged with the first clamping block 391 at the upper end and the first clamping groove 390 to seal the mixing frame 310 to prevent leakage. When unloading is required, the clamping plate can be directly rotated downward around the rotating shaft 394.

[0043] During use, the solid polypeptide is directly poured from the feed hopper 370, and then the solid polypeptide enters the stirring frame 310. When the solid polypeptide is stirred, the discharge plate 392 is opened, and then the two vibration motors 110 are started. The vibration motors 110 will make the two inclined plates 330 vibrate up and down. When the inclined plates 330 vibrate, they will respectively drive the first limiting rods 140 in the four limiting holes 380 to move up and down, and the first limiting rods 140 will drive the vibration plate 120 to move up and down. When the vibration plate 120 moves, the vertical plate 130 at one end moves synchronously. When the vertical plate 130 moves, the viscosity of the solid polypeptide between the two vertical plates 130 is greatly reduced, thereby increasing the speed of unloading; when vibrating, the four second limiting rods on a section of the vibration plate 120 close to the inclined plate 330 150 will move up and down in the limiting cylinder 160, and the speed of resetting will be greatly accelerated under the action of the spring 170, and the vibration amplitude will also be increased to a certain extent; when unloading, the polypeptide will pass through the filter screen 181 in the filter plate 180, thereby filtering some impurities, and the remaining impurities will be at the upper end of the filter screen 181 and be trapped by the surrounding inner circle of the filter plate 180. When it is used for a long time, it will need to be cleaned. At this time, grab the handle 184 to pull the filter plate 180 outward, and the second block 183 at the top of the other side of the filter plate 180 will be disengaged from the second slot 322 in the second mounting slot 321, and then moved out of the first mounting slot 320. At this time, the filter screen 181 can be cleaned. When the cleaning is completed, the filter plate 180 can be directly reset according to the opposite operation.

[0044] It is understood that the present invention is described by some embodiments, and those skilled in the art are aware that various changes or equivalent substitutions may be made to these features and embodiments without departing from the spirit and scope of the present invention. In addition, under the teachings of the present invention, these features and embodiments may be modified to adapt to specific circumstances and materials without departing from the spirit and scope of the present invention. Therefore, the present invention is not limited to the specific embodiments disclosed herein, and all embodiments falling within the scope of the claims of this application are within the scope of protection of the present invention.

Claims

1. A solid-state mixing device for producing polypeptides, It is characterized in that include: A mounting assembly (300), the mounting assembly (300) comprising a stirring frame (310); an inclined plate (330) is mounted on the inner side wall of the stirring frame (310); a vibration motor (110) is mounted on one end of any inclined plate (330); a first mounting groove (320) is provided at one end of the stirring frame (310); a second mounting groove (321) is provided at the other end of the stirring frame (310) away from the first mounting groove (320); a second clamping groove (322) is provided in the second mounting groove (321); A vibrating unloading assembly (100), the vibrating unloading assembly (100) comprising two vibrating plates (120) mounted on the inner side wall of a stirring frame (310), one end of any one of the vibrating plates (120) being mounted with a connecting block, four corners of one side of the vibrating plate (120) being mounted with first limiting rods (140), the same end of the vibrating plate (120) being mounted with four second limiting rods (150), the outer end of any one of the second limiting rods (150) being mounted with a limiting cylinder (160), any one of the limiting cylinders (160) being mounted with a spring (170), the two vibrating plates (120) A vertical plate (130) is installed at one of the opposite ends; a sliding groove (190) is symmetrically opened at the inner end of any of the vertical plates, a filter plate (180) is installed in the sliding groove (190), a filter screen (181) is installed in the filter plate (180), the filter screen (181) is installed at the lowermost end of the inner wall of the filter plate (180), a second clamping block (183) is installed at one end of the filter plate (180), a handle (184) is installed at the other end of the filter plate (180) away from the second clamping block (183), and the second clamping block (183) and the second clamping groove (322) are engaged with each other; A stirring assembly (200).

2. A solid-state mixing device for producing polypeptides according to claim 1, It is characterized in that One end of the spring (170) close to the second limiting rod (150) is connected to one end of the second limiting rod (150) close to the limiting cylinder (160).

3. A solid-state mixing device for producing polypeptides according to claim 1, It is characterized in that Four brackets (340) are installed at the four corners of one end of the stirring frame (310), and limiting holes (380) are provided at the four corners of one end of any inclined plate (330). A first connecting hole (350) is provided at one end of the stirring frame (310), and a first clamping groove (390) is provided at one end of the stirring frame (310). Any one of the first limiting rods (140) is installed in the limiting hole (380) on the inclined plate (330), and any one of the limiting cylinders (160) is connected to one end of the inclined plate (330) close to the limiting cylinder (160).

4. A solid-state mixing device for producing polypeptides according to claim 1, It is characterized in that A feed hole (360) is provided at one end of the stirring frame (310), and a feed hopper (370) is installed at one end of the stirring frame (310). An end of the feed hopper (370) close to the stirring frame (310) is connected to the feed hole (360), and a diameter of the feed hole (360) is smaller than an inner circle diameter of an end of the feed hopper (370) close to the stirring frame (310).

5. A solid-state mixing device for producing polypeptides according to claim 1, It is characterized in that The stirring assembly (200) comprises a motor (210), a stirring shaft (220) is mounted on one end of the motor (210), a bearing (240) is mounted on the other end of the stirring shaft (220), a stirring rod (230) is mounted on the stirring shaft (220), a spiral blade (259) is mounted on the stirring shaft (220), the motor (210) is mounted on one end of the stirring frame (310), and the bearing (240) is mounted on the other end of the inner wall of the stirring frame (310) away from the motor.

6. A solid-state mixing device for producing polypeptides according to claim 1, It is characterized in that Two mounting blocks (393) are installed at one end of the stirring frame (310), a rotating shaft (394) is installed between the two mounting blocks (393), a discharge plate (392) is installed outside the rotating shaft (394), and a first clamping block (391) is installed at one end of the inclined plate (330), and the first clamping block (391) is engaged with the first clamping groove (390).

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