Medicine synthesis equipment for calcium acetate oral solution
By setting up a screening mechanism and auxiliary components in the reactor of the calcium acetate oral solution synthesis equipment, the problem of insufficient mixing of solid raw materials and liquid raw materials is solved, and efficient synthesis of calcium acetate oral solution is achieved.
Patent Information
- Application Number
- CN202421110139.7
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-05-21
- Publication Date
- 2025-02-11
- Estimated Expiration
- 2034-05-21
AI Technical Summary
During the synthesis of calcium acetate oral solution, the mixture of solid raw materials and liquid raw materials is insufficient, resulting in a prolonged synthesis time and affecting the synthesis rate.
A pharmaceutical synthesis equipment for oral calcium acetate oral solution was designed. By setting up a screening mechanism and auxiliary components in the reactor, the screening and secondary screening of solid raw materials are realized, and the contact area between the raw materials is increased.
Through screening and secondary screening operations, the mixing of solid raw materials and liquid raw materials is significantly accelerated, and the overall synthesis rate of calcium acetate oral solution is improved.
Smart Images
Figure CN222446505U_ABST
Abstract
Description
Technical Field
[0001] The utility model relates to the technical field of synthesis equipment, in particular to medicine synthesis equipment for calcium acetate oral solution. Background Art
[0002] In the synthesis process of calcium acetate oral solution, it is necessary to mix the solid raw materials and liquid raw materials required for the synthesis of calcium acetate oral solution. In the prior art, the raw materials are fed into the interior of the reactor, and the purpose of mixing the raw materials is achieved through the reactor and the stirring rod provided inside the reactor.
[0003] However, when the solid raw materials and the liquid raw materials are stirred and mixed by a stirring rod, some of the solid raw materials may not be mixed sufficiently, resulting in the overall synthesis time being extended and affecting the overall synthesis rate.
[0004] The main reason for the above problems is that the interior of the reactor is a whole, and there is no device to limit the staying position of the solid raw materials. As a result, after the solid raw materials and liquid raw materials are loaded into the interior of the reactor, the solid raw materials will first accumulate at the bottom of the reactor. At this time, some of the blocked solid raw materials cannot directly contact and mix with other raw materials, which makes the overall synthesis rate of calcium acetate oral solution slow. In response to the above problems, we propose a pharmaceutical synthesis equipment for calcium acetate oral solution. Utility Model Content
[0005] In view of the shortcomings of the prior art, the utility model provides a synthesis device, which solves the problem that when the solid raw materials and liquid raw materials are stirred and mixed by a stirring rod, some solid raw materials are not mixed sufficiently, resulting in the overall synthesis time being prolonged and affecting the overall synthesis rate.
[0006] To achieve the above purpose, the utility model is implemented by the following technical scheme: a pharmaceutical synthesis device for calcium acetate oral solution, comprising a reaction kettle and a stirring rod rotatably connected to the reaction kettle, wherein a screening mechanism is arranged inside the reaction kettle, and the screening mechanism comprises:
[0007] A first mesh plate and a second mesh plate, which are fixedly arranged inside the reaction kettle, and the first mesh plate is located on the upper part of the second mesh plate;
[0008] The auxiliary component is arranged outside the stirring rod, and the raw materials on the two groups of mesh plates are further screened by the auxiliary component.
[0009] Preferably, the auxiliary components include:
[0010] The scrapers are fixedly arranged on the outer wall of the stirring rod, and the bottom end surfaces of the plurality of scrapers are respectively against the top end surfaces of the first mesh plate and the second mesh plate;
[0011] The solid block is arranged at one end of the scraper away from the stirring rod, and a plurality of groups of the solid blocks intermittently collide with the first mesh plate and the second mesh plate respectively.
[0012] Preferably, the top end surfaces of the first mesh plate and the second mesh plate are both fixedly connected with an arc seat, and the outer wall of the solid block is slidably connected to the outer wall of the arc seat.
[0013] Preferably, one end of the scraper away from the stirring rod is fixedly connected to a guide frame, and one end of the solid block is slidably connected along the outer wall of the guide frame.
[0014] Preferably, a slide plate is provided on the outer wall of the guide frame for limited sliding, and the top end surface of the solid block is fixedly connected to the bottom end surface of the slide plate.
[0015] Preferably, a driving motor for driving the stirring rod to rotate is provided on the top end surface of the reaction kettle.
[0016] Preferably, a feeding port is provided on the top end surface of the reactor.
[0017] The utility model discloses a medicine synthesis device for calcium acetate oral solution, which has the following beneficial effects: the medicine synthesis device for calcium acetate oral solution can perform screening operation on solid raw materials required for synthesis of calcium acetate oral solution by arranging a screening mechanism on the inner wall of the synthesis device, and then crush and perform secondary screening operation on solid raw materials of different volumes in combination with auxiliary components, thereby increasing the contact area between solid raw materials of different volumes and liquid raw materials, thereby accelerating the mixing between the raw materials and improving the overall synthesis rate of the calcium acetate oral solution. BRIEF DESCRIPTION OF THE DRAWINGS
[0018] In order to more clearly illustrate the embodiments of the utility model or the technical solutions in the prior art, the drawings required for use in the embodiments or the description of the prior art will be 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 paying creative work.
[0019] Figure 1 It is a schematic diagram of the overall structure of the utility model;
[0020] Figure 2 This is a cross-sectional view of the internal structure of the reactor of the utility model;
[0021] Figure 3 This is a schematic diagram of the structure of the stirring rod and the first mesh plate of the utility model;
[0022] Figure 4 For this utility model Figure 3A magnified view of the structure in the middle.
[0023] In the figure, 1, reactor; 101, feed port; 2, stirring rod; 201, drive motor; 301, first mesh plate; 302, second mesh plate; 303, auxiliary component; 3031, scraper; 3032, guide frame; 3033, slide plate; 3034, solid block; 3035, arc seat. DETAILED DESCRIPTION
[0024] In order to make the purpose, technical solution and advantages of the embodiments of the utility model clearer, the technical solution in the embodiments of the utility model is described clearly and completely. Obviously, the described embodiments are part of the embodiments of the utility model, not all of the embodiments. Based on the embodiments of the utility model, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the utility model.
[0025] The embodiment of the present application provides a synthesis device to solve the problem that when the solid raw materials and liquid raw materials are stirred and mixed by a stirring rod, some solid raw materials are not mixed sufficiently, resulting in the overall synthesis time being prolonged and affecting the overall synthesis rate, thereby achieving layered screening and melting of the solid raw materials.
[0026] In order to better understand the above technical solution, the above technical solution will be described in detail below in conjunction with the accompanying drawings and specific implementation methods.
[0027] The utility model embodiment discloses a medicine synthesis device for calcium acetate oral solution.
[0028] According to the attached Figure 1-4 As shown, it includes a reactor 1 and a stirring rod 2 rotatably connected to the reactor 1. A driving motor 201 for driving the stirring rod 2 to rotate is arranged on the top end surface of the reactor 1. A loading port 101 is provided on the top end surface of the reactor 1. When synthesizing the calcium acetate oral solution, the fixed raw materials and liquid raw materials required for the synthesis of the calcium acetate oral solution are first loaded into the reactor 1 through the loading port 101, and then the driving motor 201 is turned on, so that the driving motor 201 controls the stirring rod 2 to stir and mix the raw materials in the reactor 1, and the preliminary required calcium acetate oral solution is formed after stirring and mixing.
[0029] A screening mechanism is provided inside the reactor 1, and the screening mechanism is mainly used to screen the solid raw materials fed into the reactor 1, so as to accelerate the melting speed of the solid raw materials. The screening mechanism includes a first mesh plate 301 and a second mesh plate 302. The first mesh plate 301 and the second mesh plate 302 are fixedly arranged inside the reactor 1, and the first mesh plate 301 is located on the upper part of the second mesh plate 302. The diameter of the mesh hole opened on the top end surface of the first mesh plate 301 is larger than the diameter of the mesh hole opened on the top end surface of the second mesh plate 302.
[0030] The auxiliary component 303 is arranged outside the stirring rod 2, and the raw materials on the two groups of mesh plates are further screened by the auxiliary component 303, that is, to prevent the solid raw materials from being blocked on the two groups of mesh plates. The auxiliary component 303 includes a scraper 3031, which is fixedly arranged on the outer wall of the stirring rod 2, and the bottom end faces of the plurality of scrapers 3031 are respectively against the top end faces of the first mesh plate 301 and the second mesh plate 302, and the solid block 3034 is arranged at one end of the scraper 3031 away from the stirring rod 2, and the plurality of solid blocks 3034 intermittently collide with the first mesh plate 301 and the second mesh plate 302. The top end faces of the first mesh plate 301 and the second mesh plate 302 are fixedly connected with an arc seat 3035, and the outer wall of the solid block 3034 is slidably connected to the outer wall of the arc seat 3035. When the solid block 3034 moves to a position in contact with the arc seat 3035, the solid block 3034 can slide along the outer wall of the arc seat 3035. When the solid block 3034 is not in contact with the arc seat 3035, the solid block 3034 moves downward under the action of its own gravity, thereby causing the solid block 3034 to collide with the top end face of the mesh plate, thereby realizing vibration cleaning of the raw materials fixed at the mesh plate.
[0031] One end of the scraper 3031 away from the stirring rod 2 is fixedly connected to the guide frame 3032, one end of the solid block 3034 is slidably connected along the outer wall of the guide frame 3032, and the outer wall of the guide frame 3032 is limited and slidably provided with a slide plate 3033, the top end surface of the solid block 3034 is fixedly connected to the bottom end surface of the slide plate 3033, and the up and down moving path of the solid block 3034 can be limited by the set guide frame 3032 and the slide plate 3033.
[0032] The pharmaceutical synthesis equipment for calcium acetate oral solution can screen the solid raw materials required for the synthesis of calcium acetate oral solution by arranging a screening mechanism on the inner wall of the synthesis equipment, and then combine with the auxiliary component 303 to crush and perform secondary screening operations on solid raw materials of different volumes, thereby increasing the contact area between solid raw materials of different volumes and liquid raw materials, thereby accelerating the mixing between the raw materials and improving the overall synthesis rate of the calcium acetate oral solution.
[0033] The above shows and describes the basic principle and main features of the utility model and the advantages of the utility model. Those skilled in the art should understand that the utility model is not limited by the above embodiments. The above embodiments and descriptions are only for explaining the principle of the utility model. Without departing from the spirit and scope of the utility model, the utility model may have various changes and improvements, which fall within the scope of the utility model to be protected. The scope of protection claimed by the utility model is defined by the attached claims and their equivalents.
Claims
1. A pharmaceutical synthesis device for calcium acetate oral solution, comprising a reaction kettle (1) and a stirring rod (2) rotatably connected to the reaction kettle (1), characterized in that: The reactor (1) is provided with a screening mechanism inside, and the screening mechanism comprises: A first mesh plate (301) and a second mesh plate (302), which are fixedly arranged inside the reaction kettle (1), and the first mesh plate (301) is located above the second mesh plate (302); An auxiliary component (303) is arranged outside the stirring rod (2), and the raw materials on the two sets of screens are further screened by the auxiliary component (303); The auxiliary component (303) comprises: A scraper (3031) is fixedly arranged on the outer wall of the stirring rod (2), and the bottom end surfaces of the plurality of scrapers (3031) are respectively against the top end surfaces of the first mesh plate (301) and the second mesh plate (302); A solid block (3034) is arranged at one end of the scraper (3031) away from the stirring rod (2), and a plurality of groups of the solid blocks (3034) intermittently collide with the first mesh plate (301) and the second mesh plate (302) respectively; The top end surfaces of the first mesh plate (301) and the second mesh plate (302) are both fixedly connected with an arc-shaped seat (3035), and the outer wall of the solid block (3034) is slidably connected to the outer wall of the arc-shaped seat (3035).
2. A pharmaceutical synthesis equipment for calcium acetate oral solution according to claim 1, characterized in that: One end of the scraper (3031) away from the stirring rod (2) is fixedly connected to a guide frame (3032), and one end of the solid block (3034) is slidably connected along the outer wall of the guide frame (3032).
3. A pharmaceutical synthesis equipment for calcium acetate oral solution according to claim 2, characterized in that: The outer wall of the guide frame (3032) is provided with a slide plate (3033) for limited sliding, and the top end surface of the solid block (3034) is fixedly connected to the bottom end surface of the slide plate (3033).
4. A pharmaceutical synthesis equipment for calcium acetate oral solution according to claim 1, characterized in that: The top end surface of the reaction kettle (1) is provided with a driving motor (201) for driving the stirring rod (2) to rotate.
5. A pharmaceutical synthesis equipment for calcium acetate oral solution according to claim 1, characterized in that: The top end surface of the reaction kettle (1) is provided with a loading port (101).