Pasty medicament electric heating and medicament mixing method

Through the combination of the rotating assembly and the air vent assembly, the problem of under-small drug crushing and heating of paste-like agents is solved, and a more efficient drug crushing and heating process is achieved.

CN119983546AInactive Publication Date: 2025-05-13NANTONG PULMONARY HOSPITAL THE SIXTH PEOPLES HOSPITAL OF NANTONG
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Patent Information

Application Number
CN202510460907.4
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2025-04-14
Publication Date
2025-05-13
Estimated Expiration
Not applicable · inactive patent

AI Technical Summary

Technical Problem

In the prior art, during the production process of paste-like agents, the drug components are easily affected by the subsequent heating reaction effect due to the not sufficient pulverization of the gaps during the crushing process. At the same time, the heating method of the electric heating wire causes the agent to adhere and affects heat conduction.

Method used

The rotating component is used to drive the electric heating component to rotate inside and outside the boiling area to avoid drug adhesion; the air outlet component uses water vapor to drive the conversion component to rotate to provide crushing power to ensure that the drug is completely crushed.

Benefits of technology

It effectively avoids the problem that the drug is not fully crushed during the crushing process, and prevents the drug from adhesion, improves the heating efficiency and thoroughness of the drug crushing, and reduces costs.

✦ Generated by Eureka AI based on patent content.

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Abstract

The invention relates to the technical field of medicine mixing, in particular to a pasty medicine electric heating and medicine mixing method which comprises a boiling box body, a rotating assembly and an electric heating assembly, and the rotating assembly and the electric heating assembly are located in the boiling box body. The boiling box body is filled with water to form a boiling area; the rotating assembly is used for driving the electric heating assembly to rotate, so that the electric heating assembly enters or is separated from a boiling area; the rotating assembly comprises an electric baffle plate arranged at the feeding hole of the boiling box body and a rotating turntable rotationally connected to the inner wall of the boiling box body through a rotating shaft; when the electric heating assembly is driven by the rotating assembly to heat water, the electric heating assembly is located in the boiling area, at the moment, the water is purified water and is not interfered by medicine components, and when medicine enters hot water in the boiling area, the electric heating assembly rotates through the rotating assembly to break away from the boiling area; the electric heating assembly is not in contact with the medicine in the whole process, and therefore no medicine adheres to the electric heating assembly.
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Description

Technical Field

[0001] The invention relates to the technical field of drug mixing, and in particular to a method for electrically heating and mixing a paste-like drug. Background Art

[0002] Ointment is a common form of topical drug preparation, widely used in the treatment of skin diseases, trauma, pain, etc. According to its composition, properties and use, ointments can be divided into the following categories: 1. Ointments: Ointments are ointments whose main ingredients are oils, usually in a semi-fluid or viscous state, and are easy to apply on the skin surface; 2. Gel type: Gel refers to an agent whose main component is colloidal substances, usually in a semi-solid or gel state, with certain adhesion and permeability; 3. Ointments: Ointments refer to ointments whose main ingredients are colloidal substances. They are often gel-like and have certain adhesion and adhesion.

[0003] During the production process of paste-like medicines, the drug ingredients need to be mixed, ground and pulverized, and then the mixed drug powder is placed in a reactor, mixed with water and heated.

[0004] At present, in the prior art, the drugs are washed and dried, and then mixed and crushed, generally using a crusher or grinder. The drug components are generally in the form of particles, leaves, and petals. The gap between the two working rollers in the crusher or grinder makes it easy for the drug components with small thickness to be put into the reactor without being crushed, affecting the subsequent heating reaction effect with water.

[0005] Furthermore, in the prior art, electric heating methods are generally used to heat the crushed and mixed drug components and water, usually a heating wire heating method, which transfers heat to the water to achieve rapid heating and boiling of the water, thereby achieving the effect of boiling the drug. However, the heating wire heating method requires the heating wire and its casing to be placed in water, and the drug will produce an ointment during the boiling process, and the ointment is easy to adhere to the casing of the heating wire. Long-term use will cause a large amount of ointment to adhere to the casing of the heating wire, affecting the heat conduction effect of the heating wire.

[0006] The purpose of the invention of this application is to solve the above-mentioned problems. Summary of the invention

[0007] In view of the above-mentioned shortcomings of the prior art, the present invention provides a method for electrically heating and mixing a paste-like medicine, which can effectively solve the existing problems.

[0008] To achieve the above objectives, the present invention is implemented through the following technical solutions: The present invention provides a method for electrically heating a paste-like medicine, comprising a boiling box, and a rotating component and an electric heating component located inside the boiling box; the boiling box is filled with water to form a boiling area; the rotating component is used to drive the electric heating component to rotate so that the electric heating component enters or leaves the boiling area; the rotating component comprises an electric baffle arranged at a feeding port of the boiling box and a rotating turntable rotatably connected to an inner wall of the boiling box through a rotating shaft, one side of the electric heating component is fixedly connected to one side of the rotating turntable, and the electric baffle is used to drive the rotating turntable to rotate; the electric baffle has an open and a closed state, when the electric baffle is in an open state, the electric heating component leaves the boiling area, and the crushed drug components enter the boiling area through the feeding port of the boiling box; when the electric baffle is in a closed state, the electric heating component enters the boiling area, and the feeding port of the boiling box is closed; a temperature sensor is arranged inside the boiling box for monitoring the temperature of the boiling area.

[0009] Furthermore, the bottom of the electric baffle is fixedly connected to a limiting rotating drum, the interior of the limiting rotating drum is rotatably connected to a limiting vertical rod via a rotating shaft, the bottom of the limiting vertical rod is slidably connected to a limiting horizontal rod via a base, and one end of the limiting horizontal rod is rotatably connected to the outer wall on the other side of the rotating disc via a rotating shaft.

[0010] Furthermore, the limiting vertical rod is slidably connected to a limiting sliding rod inside, and sliding blocks are arranged on both sides of the limiting sliding rod to slide on the inner walls on both sides of the boiling box.

[0011] Further, including: S1: adding water to the boiling area in the boiling box, and starting the electric heating component to heat the water in the boiling area; S2: When the temperature sensor senses that the water temperature in the boiling area reaches 100°C, the electric heating component is turned off until the temperature sensor senses that the water temperature in the boiling area drops below 90°C, and then the electric heating component is started again to heat the water in the boiling area; S3: When the drug components are crushed, the electric baffle is started to feed the crushed drug components from the feed port of the boiling box into the boiling area to mix with the hot water therein, and at the same time, the electric heating component rotates away from the boiling area; S4: After the drug ingredients and the hot water in the boiling area are mixed for 60 minutes, the filtrate is filtered and taken.

[0012] A medicine mixing method for paste-like medicines, comprising a traction component, an air outlet component arranged on one side of the boiling box, a detachable crushing box arranged above the boiling box, a conversion component arranged on one side of the crushing box, and a crushing component located inside the crushing box; the traction component is fixedly connected to one side of the crushing box, and the traction component is located on one side of the conversion component; the air outlet component is used to transfer the heat dissipated by hot water in the boiling area to the conversion component; the conversion component is used to convert thermal energy into mechanical energy, so that the crushing component rotates to crush the drug components.

[0013] Furthermore, the air outlet component is communicated with the interior of the boiling box and has an arc shape; the size of the air outlet of the air outlet component is smaller than the size of the air inlet of the air outlet component.

[0014] Furthermore, the conversion component includes a rotating connecting plate, which is machined with supporting connecting rods around it, and an elastic telescopic column is arranged inside the supporting connecting rod, and the telescopic end of the elastic telescopic column is fixedly connected to an extension connecting plate; the outer wall of one side of the extension connecting plate is fixedly connected to an extension magnet block through a connecting rod; the traction component includes a positioning connecting rod fixed to one side of the crushing box, one side of the positioning connecting rod is fixedly connected to a magnet bar, one side of the magnet bar is fixedly connected to a baffle plate, and the magnet bar is used to attract the extension magnet block so that the extension connecting plate is close to the baffle plate; the crushing component includes a first crushing roller and a second crushing roller that rotate inside the crushing box through a rotating shaft, the first crushing roller and the second crushing roller are driven by gears, and the first crushing roller is fixedly connected to the rotating connecting plate.

[0015] Furthermore, the first crushing roller and the second crushing roller are provided with extrusion rings which are spaced apart from each other, a telescopic spring is provided inside the extrusion ring of the second crushing roller, and one end of the telescopic spring is fixedly connected to an extrusion block; a spiral sheet is provided between two adjacent extrusion rings on the second crushing roller; a spiral groove is provided on the extrusion ring of the first crushing roller, and the spiral sheet of the second crushing roller and the spiral groove of the first crushing roller are fitted and transmitted to each other.

[0016] Furthermore, the shape of the magnet bar is an arc with the center of the rotating disk as the center and the angle between two adjacent supporting connecting rods as the arc.

[0017] Further, including: S1: Wash the various drug ingredients, dry them, and then put them into a crushing box; S2: The heat of the boiling area transferred by the gas outlet component causes the conversion component to rotate, converting the thermal energy into mechanical energy, causing the first pulverizing roller and the second pulverizing roller to rotate to pulverize the drug components.

[0018] Beneficial Effects Compared with the known public technology, the technical solution provided by the present invention has the following beneficial effects: When the electric heating component is driven by the rotating component to heat the water, the electric heating component is located inside the boiling area. At this time, the water is pure water without interference from drug components. When the drug enters the hot water in the boiling area, the electric heating component is rotated by the rotating component to leave the boiling area, so that the electric heating component does not contact the drug throughout the process, so that no drug adheres to it; The gap is squeezed at the corresponding overlapped portion of the first and second crushing rollers by the telescopic spring on the second crushing roller and the squeeze block connected thereto, that is, at this time, the squeeze block abuts against the squeeze ring on the first crushing roller, thereby impact-crushing the leaf-shaped medicine therein, and the leaf-shaped medicine component passing vertically between the first and second crushing rollers is cut by the spiral blade on the second crushing roller, thereby ensuring the thoroughness of the medicine crushing and preventing the leaf-shaped medicine from entering the boiling area without being crushed; The steam ejected from the gas outlet assembly drives the telescopic connecting rod to rotate, thereby driving the conversion assembly to rotate, so that the thermal energy is converted into mechanical energy, and then the pulverizing assembly fixed to the rotating connecting plate is operated to pulverize the drug ingredients. The heat lost in the process of heating water is used as the power source for pulverizing the drug, which improves energy utilization and reduces costs. The arc-shaped air outlet component can transfer the water vapor generated in the boiling area to the bottom of the conversion component. The air outlet of the air outlet component is smaller than the air inlet of the air outlet component, so that the speed of the water vapor is increased when it moves from the air inlet of the air outlet component to the air outlet, which is convenient for subsequent blowing of the conversion component. BRIEF DESCRIPTION OF THE DRAWINGS

[0019] In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings required for use in the embodiments or the prior art descriptions are briefly introduced below. Obviously, the drawings described below are only some embodiments of the present invention, and for ordinary technicians in this field, other drawings can be obtained based on these drawings without creative work.

[0020] Figure 1 It is a schematic diagram of the overall structure of the present invention; Figure 2 It is a structural schematic diagram of the traction assembly of the present invention; Figure 3 It is a schematic diagram of the explosion structure of the conversion component of the present invention; Figure 4 It is a structural schematic diagram of the crushing assembly of the present invention; Figure 5 It is a schematic cross-sectional structure diagram of the second pulverizing roller of the present invention; Figure 6 It is a schematic diagram of the internal structure of the extrusion block of the present invention; Figure 7 It is a schematic diagram of the exploded structure of the rotating assembly of the present invention; Figure 8 Schematic diagram of the workflow of the conversion component of the present invention; Fig. 9 It is a schematic diagram of the working process of the rotating component of the present invention.

[0021] Reference numerals 100-crushing box; 200-boiling box; 300-air outlet assembly; 400-traction assembly; 401-positioning connecting rod; 402-shielding plate; 403-magnetic strip; 500-conversion assembly; 501-rotating connecting disk; 502-supporting connecting rod; 503-elastic telescopic column; 504-extension connecting plate; 505-extension magnet block; 600-crushing assembly; 610-first crushing roller; 620-second crushing roller; 621-spiral sheet; 622-extrusion block; 623-telescopic spring; 700-electric heating assembly; 701-rotating disc; 702-limiting horizontal rod; 703-limiting vertical rod; 704-limiting rotating drum; 705-electric baffle; 706-limiting sliding rod. DETAILED DESCRIPTION

[0022] Embodiments of the present disclosure will be described in more detail below with reference to the accompanying drawings. Although certain embodiments of the present disclosure are shown in the accompanying drawings, it should be understood that the present disclosure can be implemented in various forms and should not be construed as being limited to the embodiments set forth herein. On the contrary, these embodiments are provided to provide a more thorough and complete understanding of the present disclosure. It should be understood that the drawings and embodiments of the present disclosure are only for exemplary purposes and are not intended to limit the scope of protection of the present disclosure.

[0023] It should also be noted that, for ease of description, only the parts related to the invention are shown in the drawings. In the absence of conflict, the embodiments and features in the embodiments of the present disclosure can be combined with each other.

[0024] It should be noted that the concepts such as "first" and "second" mentioned in the present disclosure are only used to distinguish different devices, modules or units, and are not used to limit the order or interdependence of the functions performed by these devices, modules or units.

[0025] It should be noted that the modifications of "one" and "plurality" mentioned in the present disclosure are illustrative rather than restrictive, and those skilled in the art should understand that unless otherwise clearly indicated in the context, it should be understood as "one or more".

[0026] The present disclosure will be described in detail below with reference to the accompanying drawings and in conjunction with embodiments.

[0027] The present invention will be further described below in conjunction with the embodiments.

[0028] Embodiment 1: A method for electrically heating a paste-like medicine, such as Figure 1 , Figure 7 As shown, it includes a boiling box 200, and a rotating component and an electric heating component 700 located inside the boiling box 200; it is worth noting that the heating coil of the electric heating component 700 is usually made of a thinner metal tube, the tube is equipped with a heating wire, and then an insulating material such as magnesium oxide powder is poured in, and the heating wire is packaged and fixed in the middle of the tube, similar to the "hot fast" sold on the market. The boiling box 200 is filled with water to form a boiling area; the boiling area is the area covered by the water inside the boiling box 200, which is mixed with the drug ingredients and heated. Heat, the rotating component is used to drive the electric heating component 700 to rotate, so that the electric heating component 700 enters or leaves the boiling area; it should be noted that when the electric heating component 700 is driven by the rotating component to heat water, the electric heating component 700 is located inside the boiling area. At this time, the water is pure water without interference from drug components. When the drug enters the hot water in the boiling area, the electric heating component 700 is rotated by the rotating component to leave the boiling area, so that the electric heating component 700 does not contact the drug throughout the process, so that no drug adheres to it; Further, the rotating assembly includes an electric baffle 705 arranged at the feed inlet of the boiling box 200 and a rotating turntable 701 rotatably connected to the inner wall of the boiling box 200 through a rotating shaft, one side of the electric heating assembly 700 is fixedly connected to one side of the rotating turntable 701, and the electric baffle 705 is used to drive the rotating turntable 701 to rotate; specifically, the bottom of the electric baffle 705 is fixedly connected to a limited rotating drum 704, and the inside of the limited rotating drum 704 is rotatably connected to a limited vertical rod 703 through a rotating shaft, and the rotating shaft is set on the limited vertical rod 703 On the inner side of the top, the bottom of the limit vertical rod 703 is slidably connected to the limit horizontal rod 702 through the base, the bottom of the limit vertical rod 703 is processed with an I-shaped block, and the inside of the limit horizontal press 702 is processed with an I-shaped groove. The arc of the I-shaped block and the I-shaped groove fits each other so that the limit vertical rod 703 moves on the limit horizontal rod 702, and one end of the limit horizontal rod 702 is rotatably connected to the outer wall of the other side of the rotating disk 701 through a rotating shaft; it is worth mentioning that when adding drug components to the boiling area, the electric baffle 705 rotates to make the drug components fall into the boiling area. In this process, Fig. 9As shown, the electric baffle 705 rotates clockwise, driving the limiting rotating drum 704 to rotate, while the limiting vertical rod 703 rotatably connected thereto remains in a vertical state and rotates accordingly (the movement of the limiting vertical rod 703 can be decomposed into downward and leftward movement, the downward movement drives the limiting horizontal rod 702 to move, and the leftward movement is the movement of the limiting vertical rod 703 on the groove of the limiting horizontal rod 702). The limiting horizontal rod 702 rotates counterclockwise under the action of the rotating disk 701, thereby rotating the electric heating component 700 to make it leave the boiling area; at the same time, In order to ensure the vertical state of the limiting vertical rod 703 and the horizontal state of the limiting horizontal rod 702, the limiting vertical rod 703 is internally slidably connected to the limiting sliding rod 706, and the limiting sliding rod 706 is provided with sliders sliding on the inner walls of the boiling box 200 on both sides. The length of the limiting sliding rod 706 is the length inside the boiling box 200, that is, the movement of the limiting sliding rod 706 inside the boiling box 200 is always horizontal, thereby supporting the limiting vertical rod 703 to always remain vertical during the movement, and also acting on the limiting horizontal rod 702 Furthermore, the electric baffle 705 has an open and closed state. When the electric baffle 705 is in the open state, the electric heating component 700 is separated from the boiling area, and the crushed medicinal components enter the boiling area through the feed port of the boiling box 200; when the electric baffle 705 is in the closed state, the electric heating component 700 enters the boiling area, and the feed port of the boiling box 200 is closed; a temperature sensor is arranged inside the boiling box 200 for monitoring the temperature of the boiling area. It should be noted that the temperature sensor is used to monitor the temperature of the water in the boiling area. When the electric heating component 700 is working, when the temperature of the water in the boiling area reaches 100°C, the electric heating component 700 stops working to reduce energy output. When the heat of the hot water in the boiling area is dissipated until the temperature of the water drops below 80°C, the electric heating component works again to heat the water, thereby avoiding the electric heating component from being easily damaged due to long-term work, and intermittent work reduces energy consumption and improves the practicality of the device.

[0029] A method for electrically heating a paste-like medicine The following steps are involved: S1: adding water to the boiling area in the boiling box 200, and starting the electric heating component 700 to heat the water in the boiling area; S2: When the temperature sensor senses that the water temperature in the boiling area reaches 100°C, the electric heating component 700 is turned off, and when the temperature sensor senses that the water temperature in the boiling area drops below 90°C, the electric heating component 700 is started again to heat the water in the boiling area; S3: When the drug components are crushed, the electric baffle 705 is started, and the crushed drug components are put into the boiling area from the feed port of the boiling box 200 to mix with the hot water therein, and at the same time, the electric heating component 700 rotates away from the boiling area; S4: After the drug ingredients and the hot water in the boiling area are mixed for 60 minutes, the filtrate is filtered and taken.

[0030] Embodiment 2: A method for mixing a paste-like medicine, such as Figure 1-6 As shown, the following innovations are made based on the first embodiment: The invention comprises a traction assembly 400, an air outlet assembly 300 arranged on one side of the boiling box 200, a detachable crushing box 100 arranged above the boiling box 200, a conversion assembly 500 arranged on one side of the crushing box 100, and a crushing assembly 600 located inside the crushing box 100; Further, the air outlet component 300 is used to transfer the heat dissipated by the hot water in the boiling area to the conversion component 500; the air outlet component 300 is communicated with the inside of the boiling box 200 and is in an arc shape; the air outlet of the air outlet component 300 is smaller than the air inlet of the air outlet component 300; it should be noted that the arc-shaped air outlet component 300 can transmit the water vapor generated in the boiling area to the bottom of the conversion component 500, and the air outlet of the air outlet component 300 is smaller than the air inlet of the air outlet component 300, so that the speed of the water vapor is increased when it moves from the air inlet of the air outlet component 300 to the air outlet, which is convenient for the subsequent blowing of the conversion component 500; Furthermore, the conversion component 500 is used to convert thermal energy into mechanical energy so that the pulverizing component 600 rotates to pulverize the drug components. The conversion component 500 includes a rotating disk 501, and the rotating disk 501 is processed with supporting connecting rods 502 around it. It should be noted that the water vapor ejected from the gas outlet component 300 drives the telescopic connecting rod 502 to rotate, thereby driving the conversion component 500 to rotate, so that the thermal energy is converted into mechanical energy, and then the pulverizing component 600 fixed to the rotating disk 501 is operated to pulverize the drug components. The heat dissipated in the process of heating water is used as the power source for pulverizing the drug, thereby improving energy utilization and reducing costs. Furthermore, in order to ensure that the water vapor can drive the conversion component 500 and the crushing component 600 to work after escaping from the air outlet component 300, the traction component 400 is fixedly connected to one side of the crushing box 100, and the traction component 400 is located on one side of the conversion component 500; the traction component includes a positioning connecting rod 401 fixed to one side of the crushing box 100, and one side of the positioning connecting rod is fixedly connected to a magnet bar 403, and one side of the magnet bar 403 is fixedly connected to a shielding plate 402. It is worth noting that the shielding plate 402 can reduce the escape of water vapor, so that the water vapor can act more on the extension connecting plate 504, and the support connecting rod 502 is internally provided with an elastic telescopic column 503. , the telescopic end of the elastic telescopic column 503 is fixedly connected with an extension connecting plate 504; the outer wall of one side of the extension connecting plate 504 is fixedly connected with an extension magnet block 505 through a connecting rod. Specifically, the extension magnet block 505 and the magnet bar 403 are located in the same plane, and the mutual adsorption between the two will not affect the rotation of the rotating component 500, nor will it affect the pushing effect of water vapor on the extension connecting plate 504. The magnet bar 403 is used to attract the extension magnet block 505 so that the extension connecting plate 504 is close to the shielding plate 402. The shape of the magnet bar 403 is an arc with the center of the rotating connecting disk 501 as the center and the angle between the two adjacent supporting connecting rods 502 as the arc. It should be noted that, Figure 8 As shown, when the extension magnet block 505 moves into the arc range of the magnet bar 403, due to the magnetic attraction, the extension magnet block 505 moves outward with the extension connecting plate 504, and the force arm of the conversion component becomes longer. At this time, the water vapor ejected from the gas outlet component 300 pushes the extension connecting plate 504, that is, the longer force arm allows a smaller force to drive the operation; In addition, in order to ensure comprehensive crushing of granular, leaf-shaped and petal-shaped drugs, the first crushing roller 610 and the second crushing roller 620 are provided with extrusion rings spaced apart from each other, and a telescopic spring 623 is provided inside the extrusion ring of the second crushing roller 620, and one end of the telescopic spring 623 is fixedly connected to an extrusion block 622; it is worth noting that when the extrusion rings spaced apart from each other on the first crushing roller 610 and the second crushing roller 620 rotate, a close relationship is formed between the first crushing roller 610 and the second crushing roller 620 to reduce the generation of gaps, and a spiral sheet 621 is provided between two adjacent extrusion rings on the second crushing roller 620; a spiral groove is provided on the extrusion ring of the first crushing roller 610, and the spiral sheet of the second crushing roller 620 is closely connected to the first crushing roller 610. The spiral grooves fit together for transmission. It should be noted that, for the gap between the extrusion ring on the first pulverizing roller 610 and the extrusion ring on the second pulverizing roller 620, it is easy for the leaf-shaped medicine to pass through it without being crushed. The telescopic spring 623 on the second pulverizing roller and the extrusion block 622 connected thereto are used to squeeze the gap at the overlapping position of the corresponding first pulverizing roller 610 and the second pulverizing roller 620. That is, at this time, the extrusion block 622 is against the extrusion ring on the first pulverizing roller 610, thereby impacting and crushing the leaf-shaped medicine therein, and for the leaf-shaped drug components that pass vertically between the first pulverizing roller 610 and the second pulverizing roller 620, they are cut by the spiral sheet 621 on the second pulverizing roller 620, thereby ensuring the thoroughness of the drug crushing and preventing the leaf-shaped medicine from entering the boiling area without being crushed.

[0031] A medicament mixing method for a paste-like medicament: The steps include: S1: washing and drying the various drug components, and then placing the various drug components into a crushing box 100; S2: The heat of the boiling area transferred by the gas outlet component 300 causes the conversion component 500 to rotate, converting the thermal energy into mechanical energy, causing the first crushing roller 610 and the second crushing roller 620 to rotate, crushing the drug components. The above embodiments are only used to illustrate the technical solutions of the present invention, rather than to limit it. Although the present invention has been described in detail with reference to the aforementioned embodiments, those skilled in the art should understand that they can still modify the technical solutions described in the aforementioned embodiments, or make equivalent replacements for some of the technical features therein. However, these modifications or replacements will not cause the essence of the corresponding technical solutions to deviate from the protection scope of the technical solutions of the embodiments of the present invention.

Claims

1. A method for electrically heating a paste-like medicine, characterized in that: It comprises a boiling box (200), and a rotating component and an electric heating component (700) located inside the boiling box (200); The boiling box (200) is filled with water to form a boiling area; The rotating component is used to drive the electric heating component (700) to rotate, so that the electric heating component (700) enters or leaves the boiling area; The rotating assembly comprises an electric baffle (705) arranged at the feed inlet of the boiling box (200) and a rotating turntable (701) rotatably connected to the inner wall of the boiling box (200) via a rotating shaft, one side of the electric heating assembly (700) is fixedly connected to one side of the rotating turntable (701), and the electric baffle (705) is used to drive the rotating turntable (701) to rotate; The electric baffle (705) has an open state and a closed state. When the electric baffle (705) is in the open state, the electric heating component (700) is separated from the boiling area, and the crushed drug components enter the boiling area through the feed opening of the boiling box (200); when the electric baffle (705) is in the closed state, the electric heating component (700) enters the boiling area, and the feed opening of the boiling box (200) is closed. A temperature sensor is arranged inside the boiling box (200) for monitoring the temperature of the boiling area.

2. The method for electrically heating a paste-like medicine according to claim 1, characterized in that: The bottom of the electric baffle (705) is fixedly connected to a limit rotating drum (704); the inside of the limit rotating drum (704) is rotatably connected to a limit vertical rod (703) via a rotating shaft; the bottom of the limit vertical rod (703) is slidably connected to a limit horizontal rod (702) via a base; one end of the limit horizontal rod (702) is rotatably connected to the outer wall of the other side of the rotating disc (701) via a rotating shaft.

3. The method for electrically heating a paste-like medicine according to claim 2, characterized in that: The limiting vertical rod (703) is slidably connected internally to a limiting sliding rod (706), and sliding blocks are provided on both sides of the limiting sliding rod (706) for sliding on the inner walls on both sides of the boiling box (200).

4. A method for electrically heating a paste-like medicine according to any one of claims 1 to 3, characterized in that: include: S1: adding water to the boiling area in the boiling box (200), and starting the electric heating component (700) to heat the water in the boiling area; S2: When the temperature sensor senses that the water temperature in the boiling area reaches 100°C, the electric heating component (700) is turned off, and when the temperature sensor senses that the water temperature in the boiling area drops below 90°C, the electric heating component (700) is started again to heat the water in the boiling area; S3: When the drug components are crushed, the electric baffle (705) is started, and the crushed drug components are fed from the feed port of the boiling box (200) into the boiling area to be mixed with the hot water therein, and at the same time, the electric heating component (700) is rotated to leave the boiling area; S4: After the drug ingredients and the hot water in the boiling area are mixed for 60 minutes, the filtrate is filtered and taken.

5. A method for mixing a paste-like medicine, applied to a method for electrically heating a paste-like medicine as claimed in any one of claims 1 to 3, characterized in that: It comprises a traction assembly (400), an air outlet assembly (300) arranged on one side of the boiling box (200), a detachable crushing box (100) arranged above the boiling box (200), a conversion assembly (500) arranged on one side of the crushing box (100), and a crushing assembly (600) located inside the crushing box (100); The traction assembly (400) is fixedly connected to one side of the crushing box (100), and the traction assembly (400) is located on one side of the conversion assembly (500); The gas outlet component (300) is used to transfer the heat lost by the hot water in the boiling area to the conversion component (500); The conversion component (500) is used to convert thermal energy into mechanical energy, so as to enable the pulverizing component (600) to rotate and pulverize the drug components.

6. The method for mixing a paste-like medicine according to claim 5, characterized in that: The gas outlet assembly (300) is in communication with the interior of the boiling box (200) and is in an arc shape; The size of the air outlet of the air outlet component (300) is smaller than the size of the air inlet of the air outlet component (300).

7. The method for mixing a paste-like medicine according to claim 6, characterized in that: The conversion assembly (500) comprises a rotating connecting plate (501), the rotating connecting plate (501) is processed with supporting connecting rods (502) on its periphery, an elastic telescopic column (503) is arranged inside the supporting connecting rod (502), and the telescopic end of the elastic telescopic column (503) is fixedly connected to an extension connecting plate (504); an outer wall on one side of the extension connecting plate (504) is fixedly connected to an extension magnet block (505) via a connecting rod; The traction assembly comprises a positioning connecting rod (401) fixed to one side of the pulverizing box (100), one side of the positioning connecting rod is fixedly connected to a magnet bar (403), one side of the magnet bar (403) is fixedly connected to a shielding plate (402), and the magnet bar (403) is used to attract the extension magnet block (505) so that the extension connecting plate (504) is close to the shielding plate (402); The pulverizing assembly (600) comprises a first pulverizing roller (610) and a second pulverizing roller (620) which are rotated inside the pulverizing box (100) via a rotating shaft, the first pulverizing roller (610) and the second pulverizing roller (620) are driven by gears, and the first pulverizing roller (610) is fixedly connected to the rotating disk (501).

8. The method for mixing a paste-like medicine according to claim 7, characterized in that: The first crushing roller (610) and the second crushing roller (620) are provided with extrusion rings that are spaced apart from each other, a telescopic spring (623) is provided inside the extrusion ring of the second crushing roller (620), and one end of the telescopic spring (623) is fixedly connected to an extrusion block (622); A spiral blade (621) is provided between two adjacent extrusion rings on the second pulverizing roller (620); a spiral groove is provided on the extrusion ring of the first pulverizing roller (610), and the spiral blade of the second pulverizing roller (620) and the spiral groove of the first pulverizing roller (610) are mutually engaged and transmitted.

9. The method for mixing a paste-like medicine according to claim 8, characterized in that: The shape of the magnet bar (403) is an arc with the center of the rotating disk (501) as the center and the angle between two adjacent supporting connecting rods (502) as the arc.

10. The method for mixing a paste-like medicine according to claim 9, characterized in that: include: S1: washing and drying the various drug components, and then placing the various drug components into a pulverizing box (100); S2: The heat of the boiling area transferred by the gas outlet component (300) causes the conversion component (500) to rotate, converting the thermal energy into mechanical energy, causing the first pulverizing roller (610) and the second pulverizing roller (620) to rotate, thereby pulverizing the drug components.