CN211676336U - Pharmacy enrichment facility - Google Patents

Pharmacy enrichment facility Download PDF

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Publication number
CN211676336U
CN211676336U CN202020068008.2U CN202020068008U CN211676336U CN 211676336 U CN211676336 U CN 211676336U CN 202020068008 U CN202020068008 U CN 202020068008U CN 211676336 U CN211676336 U CN 211676336U
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controller
steam
chamber
online
evaporation chamber
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CN202020068008.2U
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Chinese (zh)
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林志展
刘俊
杨鹏军
梁传颂
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Jiangsu Utions Technology Co ltd
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Jiangsu Utions Technology Co ltd
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Abstract

The utility model relates to a pharmacy enrichment facility, it includes: a heating chamber; an evaporation chamber; the steam inlet pipe is connected into the heating cavity, a steam pneumatic adjusting valve is arranged on the steam inlet pipe, and a steam pressure detector is also arranged on the steam inlet pipe; the vacuum pneumatic regulating valve is arranged on the evaporation chamber; the input end of the controller is connected with the steam pressure detector, and the output end of the controller is respectively connected with the steam pneumatic regulating valve and the vacuum pneumatic regulating valve; the online temperature detector is arranged in the evaporation chamber and is connected with the input end of the controller; and the online liquid level detector is arranged in the evaporation chamber and is connected with the input end of the controller. So that the foaming control and the temperature control of the material are more stable.

Description

Pharmacy enrichment facility
Technical Field
The utility model relates to a pharmacy enrichment facility.
Background
In the process of medicine concentration, the control of temperature influences the quality of concentration and the safety of materials, and the conventional temperature control mostly adopts a manual adjustment manual steam valve, so that the defects of low efficiency, easy material running and unstable quality exist. Improvements are therefore needed.
SUMMERY OF THE UTILITY MODEL
The utility model aims to provide a pharmacy enrichment facility has improved the quality of concentrated operation.
In order to achieve the above purpose, the utility model adopts the technical scheme that:
the utility model provides a pharmacy enrichment facility, it includes:
the heating chamber is internally provided with a plurality of parallel tubes, the upper ends and the lower ends of the tubes are respectively provided with a sealing plate I and a sealing plate II, heating cavities are formed between the sealing plate I and the sealing plate II and between the tubes, a staying cavity I is arranged above the sealing plate I, a staying cavity II is arranged below the sealing plate II, and the upper ends and the lower ends of the tubes are respectively communicated with the staying cavity I and the staying cavity II;
the evaporation chamber is provided with a circulating pipe I between the evaporation chamber and the staying cavity I, and a circulating pipe II between the evaporation chamber and the staying cavity II;
the steam inlet pipe is connected into the heating cavity, a steam pneumatic adjusting valve is arranged on the steam inlet pipe, and a steam pressure detector is also arranged on the steam inlet pipe;
a vacuum pneumatic regulating valve disposed on the evaporation chamber;
the input end of the controller is connected with the steam pressure detector, and the output end of the controller is respectively connected with the steam pneumatic regulating valve and the vacuum pneumatic regulating valve;
the online temperature detector is arranged in the evaporation chamber and is connected with the input end of the controller;
and the online liquid level detector is arranged in the evaporation chamber and is connected with the input end of the controller.
Optionally, it further comprises:
and the online pressure detector is connected to the input end of the controller.
Further, it also includes:
and the alarm mechanism is connected with the controller, and the starting of the alarm mechanism is related to the monitoring value of the steam pressure detector.
Optionally, a PID loop is provided in the controller.
Optionally, the evaporation chamber further comprises a feeding pipe and a feeding branch pipe, wherein the feeding pipe is connected with the staying chamber II, one end of the feeding branch pipe is connected with the feeding pipe, and the other end of the feeding branch pipe extends into the evaporation chamber.
Because of the application of the technical scheme, compared with the prior art, the utility model has the following advantages:
the utility model discloses a pharmacy enrichment facility, thereby owing to advance to manage at steam and set up the steam pressure that the monitoring of steam pressure detector was admitted air, online liquid level detector monitoring liquid level condition (liquid level monitoring value risees when the liquid medicine bubbles), online temperature detector monitoring temperature condition to feed back liquid level condition and temperature condition to the controller, the controller adjusts heating steam's speed and vacuum value size through adjusting steam pneumatic control valve and vacuum pneumatic control valve. So that the foaming control and the temperature control of the material are more stable.
Drawings
Some specific embodiments of the present invention will be described in detail hereinafter, by way of illustration and not by way of limitation, with reference to the accompanying drawings. The same reference numbers in the drawings identify the same or similar elements or components. Those skilled in the art will appreciate that the drawings are not necessarily drawn to scale. In the drawings:
fig. 1 is a schematic structural view of a pharmaceutical concentrator according to a preferred embodiment of the present invention;
FIG. 2 is a schematic diagram of the input and output connections of the controller;
wherein the reference numerals are as follows:
1. a heating chamber;
2. an evaporation chamber;
3. arranging pipes;
4. a sealing plate I;
5. a closing plate II;
6. a heating cavity;
7. a staying cavity I;
8. a staying cavity II;
9. a circulating pipe I;
10. a circulating pipe II;
11. a steam inlet pipe;
12. a steam pneumatic regulating valve;
13. a steam pressure detector;
14. a vacuum pneumatic regulating valve;
15. a controller;
16. an online temperature detector;
17. an online liquid level detector;
18. an online pressure detector;
19. an alarm mechanism;
20. a feed pipe;
21. a feed branch pipe;
22. a discharge pipe;
23. a condensing hydrophobic bypass pneumatic valve.
Detailed Description
The technical solution of the present invention will be described clearly and completely with reference to the accompanying drawings, and obviously, the described embodiments are some, but not all embodiments of the present invention. Based on the embodiments in the present invention, all other embodiments obtained by a person skilled in the art without creative work belong to the protection scope of the present invention.
In the description of the present invention, it should be noted that the terms "center", "upper", "lower", "left", "right", "vertical", "horizontal", "inner", "outer", and the like indicate orientations or positional relationships based on the orientations or positional relationships shown in the drawings, and are only for convenience of description and simplification of description, but do not indicate or imply that the device or element referred to must have a specific orientation, be constructed and operated in a specific orientation, and thus, should not be construed as limiting the present invention. Furthermore, the terms "first," "second," and "third" are used for descriptive purposes only and are not to be construed as indicating or implying relative importance.
Furthermore, the technical features mentioned in the different embodiments of the invention described below can be combined with each other as long as they do not conflict with each other.
As shown in fig. 1, the pharmaceutical concentration apparatus includes a heating chamber 1 and an evaporation chamber 2.
The heating chamber 1 is provided with a plurality of tubes 3 arranged in parallel, and the tubes 3 extend in the vertical direction and are independent of each other. The upper end and the lower extreme of tubulation 3 are provided with shrouding I4 and shrouding II 5 respectively, and the top of shrouding I4 is provided with the below that stops chamber I7, shrouding II 5 and is provided with and stops chamber II 8. The upper end and the lower end of the tube array 3 are respectively opened in a staying cavity I7 and a staying cavity II 8.
A circulating pipe I9 is arranged between the staying cavity I7 and the evaporation chamber 2, and two ends of the circulating pipe I9 are respectively communicated with the staying cavity I7 and the evaporation chamber 2. A circulating pipe II 10 is arranged between the staying cavity II 8 and the evaporation chamber 2, and two ends of the circulating pipe II 10 are respectively communicated with the staying cavity II 8 and the evaporation chamber 2.
Sealed heating cavities 6 are formed between the sealing plates I4 and II 5 and between the tubes 3. A steam inlet pipe 11 is connected into the heating cavity 6, and high-temperature steam is introduced into the heating cavity 6 through the steam inlet pipe 11. The liquid medicine to be heated is loaded in the tube array 3, flows into the lower end of the tube array 3 from the staying cavity II 8, and flows out from the upper end of the tube array 3 to enter the staying cavity I7. The liquid medicine is heated by the high-temperature steam in the heating cavity 6 in the process of flowing through the tube array 3 and boils in the staying cavity I7, and is sprayed out to the evaporation chamber 2 through the circulating tube I9, and the liquid medicine is evaporated and concentrated in the evaporation chamber 2. The cooled liquid medicine in the evaporation chamber 2 enters the retention chamber II 8 through the circulating pipe II 10 and further enters the tube nest 3 to be heated, and the process is repeated.
As shown in fig. 1, the bottom of the heating chamber 1 is provided with a discharge pipe 22, and the discharge pipe 22 is connected to the heating chamber 6 for discharging steam and condensed water. A condensate trap bypass pneumatic valve 23 is provided on the discharge pipe 22. As shown in fig. 2, the condensate trap bypass pneumatic valve 23 is connected to the output of the controller 15 and controlled.
The heating chamber 1 and the evaporation chamber 2 are in a vacuum state to boil the chemical liquid at a low boiling point.
In order to monitor and adjust the pressure of the heating steam in real time, a steam pressure detector 13 and a steam pneumatic adjusting valve 12 are arranged on the steam inlet pipe 11. Referring to fig. 2, the steam pressure detector 13 is connected to an input end of a controller 15, an output end of the controller 15 is connected to the steam pneumatic regulating valve 12, and when the pressure value exceeds or is lower than a set value, the steam pneumatic regulating valve 12 is automatically regulated.
As shown in fig. 1, a vacuum pneumatic control valve 14 is further provided in the evaporation chamber 2, and the degree of vacuum is controlled by the vacuum pneumatic control valve 14. An online pressure detector 18 is also arranged in the evaporation chamber 2 and used for monitoring the pressure in the evaporation chamber 2. Referring to fig. 2, the in-line pressure detector 18 is connected to an input of the controller 15, and the vacuum pneumatic control valve 14 is connected to an output of the controller 15. When the on-line pressure detector 18 monitors that the volume pressure exceeds a set range (lower or higher), the controller 15 adjusts the vacuum degree by adjusting the vacuum pneumatic adjusting valve 14.
An online temperature detector 16 is also arranged in the evaporation chamber 2, and the online temperature detector 16 monitors the temperature in the evaporation chamber 2 in real time. In the process of medicine concentration, the control of temperature influences the quality of concentration and the safety of materials. Therefore, it is important to control the temperature of the liquid medicine. The online temperature detector 16 is connected to an input end of the controller 15, and the controller 15 controls the steam pneumatic regulating valve 12 and the vacuum pneumatic regulating valve 14 according to a temperature value monitored by the online temperature detector 16, so that the temperature and the pressure are within respective set ranges and are in a stable and balanced state. A PID loop may be provided in the controller 15 for precise control.
An online liquid level detector 17 is also arranged in the evaporation chamber 2 and used for detecting the material liquid level of the evaporator. Referring to FIG. 2, an in-line level detector 17 is connected to an input of the controller 15. When the liquid level is abnormally increased due to bubbles generated in the liquid medicine in the concentration process, the controller 15 controls the steam pneumatic control valve 12 and the evaporator vacuum pneumatic control valve 14 to adjust the balance of the evaporator online pressure detector 18 and the evaporator online temperature detector 16, so that the detection data of the evaporator online liquid level detector 17 is reduced, the bubbles are eliminated, and the occurrence of the material leakage condition is avoided.
Referring to fig. 2, the present embodiment further includes an alarm mechanism 19, the alarm mechanism 19 is connected to the output terminal of the controller 15, and the alarm mechanism 19 is associated with the monitoring value of the steam pressure detector 13. When the steam pressure detector 13 is controlled to be abnormal, the alarm mechanism 19 is started to give an alarm, so that the safety is improved.
Referring to fig. 1, a feed pipe 20 is provided at the bottom of the heating chamber 1, the feed pipe 20 is connected to the residence chamber ii 8, and the material (chemical liquid) is fed into the residence chamber ii 8 through the feed pipe 20 before the evaporation concentration operation is started. However, if the feed is fed to the retention chamber II 8 during the operation of the evaporative concentration, a large amount of bubbles are generated.
To solve this problem, a feed branch pipe 21 is further provided, one end of the feed branch pipe 21 being connected to the feed pipe 20, and the other end of the feed branch pipe 21 extending into the evaporation chamber 2. During the operation of the evaporation concentration, if the material is fed, the material is conveyed to the evaporation chamber 2 through the feeding branch pipe 21 instead of being fed to the retention chamber II 8, and in this way, a large amount of bubbles are not generated during the feeding.
The pharmacy enrichment facility of this example can realize the stable control of pharmacy concentration temperature, keeps high-efficient, stable with the concentrated production process of pharmacy, avoids the material to produce the foam of bumping and run out the material, and the production environment is in balanced state, reaches ideal intelligent temperature control, and the result of use is good.
The above embodiments are only for illustrating the technical concept and features of the present invention, and the purpose thereof is to enable those skilled in the art to understand the contents of the present invention and to implement the present invention, so as not to limit the protection scope of the present invention, and all equivalent changes or modifications made according to the spirit of the present invention should be covered by the protection scope of the present invention.

Claims (5)

1. A pharmaceutical compression apparatus, comprising:
the device comprises a heating chamber (1), wherein a plurality of parallel tubes (3) are arranged in the heating chamber (1), the upper ends and the lower ends of the tubes (3) are respectively provided with a sealing plate I (4) and a sealing plate II (5), heating cavities (6) are formed between the sealing plates I (4) and the sealing plates II (5) and between the tubes (3), a staying cavity I (7) is arranged above the sealing plate I (4), a staying cavity II (8) is arranged below the sealing plate II (5), and the upper ends and the lower ends of the tubes (3) are respectively communicated with the staying cavity I (7) and the staying cavity II (8);
the device comprises an evaporation chamber (2), wherein a circulating pipe I (9) is arranged between the evaporation chamber (2) and a staying cavity I (7), and a circulating pipe II (10) is arranged between the evaporation chamber (2) and a staying cavity II (8);
the steam inlet pipe (11) is connected into the heating cavity (6), a steam pneumatic regulating valve (12) is arranged on the steam inlet pipe (11), and a steam pressure detector (13) is further arranged on the steam inlet pipe (11);
a vacuum pneumatic regulating valve (14), the vacuum pneumatic regulating valve (14) being arranged on the evaporation chamber (2);
the input end of the controller (15) is connected with the steam pressure detector (13), and the output end of the controller (15) is respectively connected with the steam pneumatic regulating valve (12) and the vacuum pneumatic regulating valve (14);
the online temperature detector (16), the online temperature detector (16) is arranged in the evaporation chamber (2), and the online temperature detector (16) is connected with the input end of the controller (15);
the online liquid level detector (17), online liquid level detector (17) set up in evaporating chamber (2), just online liquid level detector (17) with the input of controller (15) is connected.
2. The pharmaceutical concentrator of claim 1, further comprising:
and the online pressure detector (18), wherein the online pressure detector (18) is connected to the input end of the controller (15).
3. The pharmaceutical concentrator of claim 2, further comprising:
the alarm mechanism (19) is connected with the controller (15), and the starting of the alarm mechanism (19) is related to the monitoring value of the steam pressure detector (13).
4. The pharmaceutical concentrator device of claim 1, wherein: and a PID loop is arranged in the controller (15).
5. The pharmaceutical concentrator device of claim 1, wherein: it still includes inlet pipe (20) and feeding branch pipe (21), inlet pipe (20) are connected stay chamber II (8), the one end of feeding branch pipe (21) is connected inlet pipe (20), the other end of feeding branch pipe (21) extends into in evaporating chamber (2).
CN202020068008.2U 2020-01-14 2020-01-14 Pharmacy enrichment facility Active CN211676336U (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202020068008.2U CN211676336U (en) 2020-01-14 2020-01-14 Pharmacy enrichment facility

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202020068008.2U CN211676336U (en) 2020-01-14 2020-01-14 Pharmacy enrichment facility

Publications (1)

Publication Number Publication Date
CN211676336U true CN211676336U (en) 2020-10-16

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ID=72771534

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202020068008.2U Active CN211676336U (en) 2020-01-14 2020-01-14 Pharmacy enrichment facility

Country Status (1)

Country Link
CN (1) CN211676336U (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111097183A (en) * 2020-01-14 2020-05-05 江苏中有信科技有限公司 Pharmacy enrichment facility

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111097183A (en) * 2020-01-14 2020-05-05 江苏中有信科技有限公司 Pharmacy enrichment facility

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