A continuous pharmaceutical liquid concentration device

Abstract

This utility model provides a continuous liquid concentration device, relating to the field of liquid concentration technology. It includes a feeding assembly and a unit liquid concentration component. The output end of the feeding assembly is connected to the unit liquid concentration component via a sleeve. A cleaning and discharging mechanism connecting to the output end of the unit liquid concentration component is provided around the feeding assembly. The unit liquid concentration component includes a lower sealing port, a concentration chamber, a shell, a heating rod, an inner lining mesh frame, and a barrier plate. This utility model primarily utilizes a sealed sleeve connection between the upper sealing port and the upper output nozzle above the concentration chamber. When the hydraulic telescopic frame above the outer end of the end-to-end frame operates, the lifting block, lifting sleeve, upper horizontal section pipe, upper horizontal connecting pipe, and upper output nozzle can collectively open the unit liquid concentration component, facilitating rapid and complete cleaning by personnel, thereby improving equipment maintenance efficiency.

Description

Technical Field

[0001] This utility model relates to the field of pharmaceutical liquid concentration technology, and in particular to a continuous pharmaceutical liquid concentration device. Background Technology

[0002] A drug concentrate separator is a medical device that can concentrate drug preparations. Its main function is to separate harmful components such as impurities and toxins from the original drug solution by combining multiple separation technologies, thereby improving the purity and activity of the drug and reducing the possibility of adverse reactions. It is widely used in the medical and health field, especially in the pharmaceutical industry and patient treatment.

[0003] Existing continuous liquid concentration equipment, such as the one described in application number CN201721621633.X which relates to the field of pharmaceutical processing equipment, specifically a traditional Chinese medicine purification device, can achieve drug extraction and concentration. This traditional Chinese medicine purification device includes a heating tank, a clear liquid storage tank, a concentration tank, and an extraction tank, which are connected sequentially. The turbid liquid after decoction enters the clear liquid storage tank for sedimentation, and is then heated and concentrated in the concentration tank. The concentrated liquid then enters the extraction tank for extraction. However, although the above technology is a unidirectional flow concentration process, its complex structure makes it difficult to perform effective and rapid internal cleaning operations. Therefore, this utility model proposes a continuous liquid concentration device to solve the problems existing in the prior art. Utility Model Content

[0004] To address the aforementioned problems, this utility model proposes a continuous liquid concentrater. This continuous liquid concentrater mainly utilizes a sealed upper sleeve and upper output nozzle for insertion and sealing at the top of the concentration chamber. When the hydraulic telescopic frame above the outer end of the end-to-end frame outputs power, the lifting block, lifting sleeve, upper horizontal section pipe, upper horizontal connecting pipe, and upper output nozzle can be opened as a whole to facilitate rapid and complete cleaning by the staff, thereby improving the equipment's maintenance efficiency.

[0005] To achieve the purpose of this utility model, the utility model is implemented through the following technical solution: a continuous medicine liquid concentration device, including a feeding assembly and a unit medicine liquid concentration component, wherein the output end of the feeding assembly is provided with a unit medicine liquid concentration component connected in a sleeve, and a cleaning and discharging mechanism connected to the output end of the unit medicine liquid concentration component is provided on the outer periphery of the feeding assembly.

[0006] The unit drug concentration component includes a lower sealing port, a concentration chamber, a shell, a heating rod, an inner lining mesh frame, and a barrier sleeve. The lower sealing port is located at the output end of the feeding assembly. The concentration chamber is located above the lower sealing port, and the outer side of the concentration chamber is provided with a shell for mounting the heating rod. The inner lining mesh frame is located inside the concentration chamber, and the outer side of the shell is provided with a barrier sleeve that is fitted in place.

[0007] In a preferred embodiment of this utility model, the inner lining mesh frame has a porous structure, and the heating rods are distributed in a ring at equal angles around the central axis of the outer shell.

[0008] In a preferred embodiment of this utility model, the feeding assembly includes a pad, bolt brackets, a bearing plate, bolt sleeves, a liquid inlet pump, a liquid inlet valve block, a lower horizontal section pipe, a lower horizontal connecting pipe, and a lower output nozzle. The bearing plate is bolted to both ends of the pad via bolt brackets, and bolt sleeves are bolted to the upper perimeter of the bearing plate. A liquid inlet pump is located at one end of each bolt sleeve, and a liquid inlet valve block is located at one end of each liquid inlet pump.

[0009] In a preferred embodiment of the present invention, a lower horizontal section tube is provided on the inner side of the bolt sleeve block, and a lower horizontal connecting tube is provided at the output end of the lower horizontal section tube, and a lower output nozzle is provided at the output end of the lower horizontal connecting tube.

[0010] In a preferred embodiment of this utility model, the cleaning and discharging mechanism includes an end frame, a hydraulic telescopic frame, a lifting block, a lifting sleeve, an upper horizontal section pipe, an upper horizontal connecting pipe, an upper output nozzle, an upper sealing sleeve, a liquid discharge pump, and a liquid discharge valve block. The end frame is arranged around the upper perimeter of the bearing plate, and a hydraulic telescopic frame is provided at the top of the end frame. The output end of the hydraulic telescopic frame is provided with a lifting block, and a lifting sleeve is provided on the inner bottom side of the lifting block.

[0011] In a preferred embodiment of this utility model, an upper horizontal section pipe is provided on the inner side of the hoisting sleeve, and an upper horizontal connecting pipe is provided on the inner side of the upper horizontal section pipe. An upper output nozzle is provided below the upper horizontal connecting pipe, and an upper sealing port is provided below the upper output nozzle. A liquid discharge pump is provided at the output end of the upper horizontal section pipe, and a liquid discharge valve block is provided at the output end of the liquid discharge pump.

[0012] The beneficial effects of this utility model are as follows:

[0013] This utility model mainly utilizes the upper sealing sleeve and upper output nozzle of the concentration chamber for sealed insertion. After the hydraulic telescopic frame above the outer end of the end frame outputs power, the lifting block, lifting sleeve, upper horizontal section pipe, upper horizontal connecting pipe, and upper output nozzle can be opened as a whole to facilitate the staff to carry out a complete and quick cleaning and disposal, thereby improving the maintenance efficiency of the equipment. Attached Figure Description

[0014] Figure 1 This is a three-dimensional structural diagram of the present invention;

[0015] Figure 2 This is a bottom-view three-dimensional structural diagram of the present invention;

[0016] Figure 3 This is a three-dimensional structural diagram of the unit drug concentration component of this utility model;

[0017] Figure 4 This is a three-dimensional structural diagram of the upper horizontal section pipe and the upper horizontal connecting pipe of this utility model.

[0018] The components include: 1. Feeding assembly; 101. Pad; 102. Bolt support; 103. Bearing plate; 104. Bolt sleeve; 105. Inlet pump; 106. Inlet valve block; 107. Lower horizontal section pipe; 108. Lower horizontal connecting pipe; 109. Lower outlet nozzle; 2. Unit liquid concentration component; 201. Lower sealing port; 202. Concentration chamber; 203. Outer shell; 204. Heating rod; 205. Inner lining mesh frame; 206. Barrier sleeve plate; 3. Cleaning and discharging mechanism; 301. End-aligning frame; 302. Hydraulic telescopic frame; 303. Lifting block; 304. Lifting sleeve block; 305. Upper horizontal section pipe; 306. Upper horizontal connecting pipe; 307. Upper outlet nozzle; 308. Upper sealing port; 309. Outlet pump; 3010. Outlet valve block. Detailed Implementation

[0019] To deepen the understanding of this utility model, the following detailed description will be provided in conjunction with embodiments. These embodiments are only used to explain this utility model and do not constitute a limitation on the scope of protection of this utility model.

[0020] according to Figure 1-4 As shown, this embodiment proposes a continuous liquid concentration device, including a feeding assembly 1 and a unit liquid concentration component 2. The output end of the feeding assembly 1 is provided with a unit liquid concentration component 2 connected in a sleeve. The outer periphery of the feeding assembly 1 is provided with a cleaning and discharging mechanism 3 connected to the output end of the unit liquid concentration component 2.

[0021] The unit liquid concentration component 2 includes a lower sealing port 201, a concentration chamber 202, a shell 203, a heating rod 204, an inner lining mesh frame 205, and a barrier sleeve 206. The lower sealing port 201 is located at the output end of the feeding component 1. The concentration chamber 202 is located above the lower sealing port 201, and the outer side of the concentration chamber 202 is provided with a shell 203 for mounting the heating rod 204. The inner lining mesh frame 205 is provided inside the concentration chamber 202, and the outer side of the shell 203 is provided with a barrier sleeve 206 that is fitted together.

[0022] The inner lining frame 205 has a porous structure, and the heating rods 204 are distributed at equal angles around the central axis of the outer shell 203.

[0023] In this embodiment, the liquid medicine is introduced into the concentration chamber 202 through the lower sealing port 201, and the inner lining mesh frame 205 is used to prevent boiling. When heating is required, the heating rod 204 on the inner side of the outer shell 203 heats the inside of the concentration chamber 202 to achieve the effect of heating and concentration.

[0024] The feeding assembly 1 includes a pad 101, a bolt bracket 102, a support plate 103, a bolt sleeve block 104, a liquid inlet pump 105, a liquid inlet valve block 106, a lower horizontal section pipe 107, a lower horizontal connecting pipe 108, and a lower output nozzle 109. The support plate 103 is bolted to both ends of the pad 101 via the bolt bracket 102. Bolt sleeve blocks 104 are bolted to the upper sides of the support plate 103. The liquid inlet pump 105 is installed at one end of the bolt sleeve block 104, and the liquid inlet valve block 106 is installed at one end of the liquid inlet pump 105.

[0025] In this embodiment, during use, the equipment is assembled with bolts through the pad 101, bolt bracket 102, and bearing plate 103, and then placed in the system so that the liquid inlet valve block 106 is opened. When the liquid inlet valve block 106 is opened, the liquid inlet pump 105 outputs power to drive the output end to run, so that the medicine is input through the liquid inlet pump 105 and the liquid inlet valve block 106.

[0026] The inner side of the bolt sleeve block 104 is provided with a lower horizontal section tube 107, and the output end of the lower horizontal section tube 107 is provided with a lower horizontal connecting tube 108, and the output end of the lower horizontal connecting tube 108 is provided with a lower output nozzle 109.

[0027] In this embodiment, after the liquid medicine is input, the inlet pump 105 and the inlet valve block 106 input the liquid into the lower horizontal section pipe 107, and then input the liquid into the lower outlet nozzle 109 through the lower horizontal section pipe 107 and the lower horizontal connecting pipe 108 and enter the unit liquid medicine concentration component 2.

[0028] The cleaning and discharging mechanism 3 includes an end frame 301, a hydraulic telescopic frame 302, a lifting block 303, a lifting sleeve block 304, an upper horizontal section pipe 305, an upper horizontal connecting pipe 306, an upper output nozzle 307, an upper sealing sleeve 308, a liquid discharge pump 309, and a liquid discharge valve block 3010. The end frame 301 is arranged around the upper perimeter of the bearing plate 103. The top of the end frame 301 is equipped with a hydraulic telescopic frame 302, and the output end of the hydraulic telescopic frame 302 is equipped with a lifting block 303. The inner bottom side of the lifting block 303 is equipped with a lifting sleeve block 304.

[0029] In this embodiment, when cleaning is required, the hydraulic telescopic frame 302 above the outer end of the end-to-end frame 301 is used to drive the output end to operate, so that the lifting block 303 and the lifting sleeve block 304 are raised to achieve effective cleaning of the unit drug concentration component 2.

[0030] The inner side of the lifting sleeve block 304 is provided with an upper horizontal section pipe 305, and the inner side of the upper horizontal section pipe 305 is provided with an upper horizontal connecting pipe 306. The lower part of the upper horizontal connecting pipe 306 is provided with an upper output nozzle 307, and the lower part of the upper output nozzle 307 is provided with an upper sealing port 308. The output end of the upper horizontal section pipe 305 is provided with a liquid discharge pump 309, and the output end of the liquid discharge pump 309 is provided with a liquid discharge valve block 3010.

[0031] In this embodiment, when multi-stage concentration is required, under pressure, the liquid medicine is circulated through the array of unit liquid medicine concentration components 2 by the cooperation of the upper output nozzle 307, the lower horizontal section pipe 107, the lower horizontal connecting pipe 108, the lower output nozzle 109, and the upper horizontal section pipe 305. The liquid medicine is also circulated by the output power of the upper liquid pump 309, which drives the output end to operate, so that the liquid outlet valve block 3010 outputs the concentrated medicine.

[0032] The working principle of this continuous liquid concentrate equipment is as follows: During use, the equipment is assembled using bolts through the pad 101, bolt bracket 102, and bearing plate 103. After placement, the inlet valve block 106 is opened, causing the inlet pump 105 to output power and drive the output end. The liquid concentrate is then input through the inlet pump 105 and inlet valve block 106. After input, the liquid concentrate is fed into the lower horizontal section pipe 107, and then through the lower horizontal connecting pipe 107 and lower outlet 109, entering the unit liquid concentrate component 2. The liquid concentrate then enters the concentration chamber 202 through the lower sealing port 201, and the inner lining mesh frame 205 is used to prevent boiling over. When heating is required, the liquid concentrate is then... The heating rod 204 on the inner side of the outer shell 203 heats the inside of the concentration chamber 202 to achieve the effect of heating and concentration. When multi-stage concentration is required, under pressure, the liquid medicine is circulated through the array of unit liquid medicine concentration components 2 by the cooperation of the upper output nozzle 307, the lower horizontal section pipe 107, the lower horizontal connecting pipe 108, the lower output nozzle 109, and the upper horizontal section pipe 305. The liquid medicine concentration components 2 are circulated by the upper liquid pump 309, which outputs power to drive the output end to operate, so that the liquid outlet valve block 3010 outputs the concentrated medicine. When cleaning is required, the hydraulic telescopic frame 302 above the outer end of the end frame 301 outputs power to drive the output end to operate, so that the lifting block 303 and the lifting sleeve block 304 are lifted to effectively clean the unit liquid medicine concentration components 2.

[0033] The foregoing has shown and described the basic principles, main features, and advantages of this utility model. Those skilled in the art should understand that this utility model is not limited to the above embodiments. The embodiments and descriptions in the specification are merely illustrative of the principles of this utility model. Various changes and modifications can be made to this utility model without departing from its spirit and scope, and all such changes and modifications fall within the scope of the claimed utility model. The scope of protection of this utility model is defined by the appended claims and their equivalents.

Claims

1. A continuous drug liquid concentration apparatus comprising a feed assembly (1) and a unit drug liquid concentration component (2), characterized in that: The output end of the feeding assembly (1) is provided with a unit medicine concentration component (2) connected in a sleeve, and a cleaning and discharging mechanism (3) connected to the output end of the unit medicine concentration component (2) is provided on the outer periphery of the feeding assembly (1). The unit drug concentration component (2) includes a lower sealing port (201), a concentration chamber (202), a shell (203), a heating rod (204), an inner lining mesh frame (205), and a barrier sleeve (206). The lower sealing port (201) is located at the output end of the feeding assembly (1). The concentration chamber (202) is located above the lower sealing port (201), and the outer side of the concentration chamber (202) is provided with a shell (203) for installing the heating rod (204). The inner lining mesh frame (205) is located inside the concentration chamber (202), and the outer side of the shell (203) is provided with a barrier sleeve (206) for sleeve installation.

2. The continuous drug solution concentration apparatus according to claim 1, wherein: The inner lining mesh frame (205) has a porous structure, and the heating rods (204) are distributed at equal angles around the central axis of the outer shell (203).

3. The continuous drug solution concentration apparatus according to claim 1, wherein: The feeding assembly (1) includes a pad (101), a bolt bracket (102), a support plate (103), a bolt sleeve (104), a liquid inlet pump (105), a liquid inlet valve block (106), a lower horizontal section pipe (107), a lower horizontal connecting pipe (108), and a lower output nozzle (109). The support plate (103) is bolted to both ends of the pad (101) via the bolt bracket (102), and bolt sleeves (104) are bolted to the upper sides of the support plate (103). A liquid inlet pump (105) is provided at one end of the bolt sleeve (104), and a liquid inlet valve block (106) is provided at one end of the liquid inlet pump (105).

4. The continuous drug solution concentration apparatus according to claim 3, wherein: The inner side of the bolt sleeve (104) is provided with a lower horizontal section tube (107), and the output end of the lower horizontal section tube (107) is provided with a lower horizontal connecting tube (108), and the output end of the lower horizontal connecting tube (108) is provided with a lower output nozzle (109).

5. The continuous drug solution concentration apparatus according to claim 3, wherein: The cleaning and discharging mechanism (3) includes an end frame (301), a hydraulic telescopic frame (302), a lifting block (303), a lifting sleeve (304), an upper horizontal section pipe (305), an upper horizontal connecting pipe (306), an upper output nozzle (307), an upper sealing sleeve (308), a liquid discharge pump (309), and a liquid discharge valve block (3010). The end frame (301) is arranged above the periphery of the bearing plate (103). The top of the end frame (301) is provided with a hydraulic telescopic frame (302), and the output end of the hydraulic telescopic frame (302) is provided with a lifting block (303). The inner bottom side of the lifting block (303) is provided with a lifting sleeve (304).

6. The continuous drug solution concentration apparatus according to claim 5, wherein: The inner side of the hoisting sleeve (304) is provided with an upper horizontal section pipe (305), and the inner side of the upper horizontal section pipe (305) is provided with an upper horizontal connecting pipe (306). The lower part of the upper horizontal connecting pipe (306) is provided with an upper output nozzle (307), and the lower part of the upper output nozzle (307) is provided with an upper sealing port (308). The output end of the upper horizontal section pipe (305) is provided with a liquid discharge pump (309), and the output end of the liquid discharge pump (309) is provided with a liquid discharge valve block (3010).

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