Assembly type disinfection sterile clean room
By designing a quick disassembly mechanism and sealing mechanism in a prefabricated disinfection and aseptic clean room, the problems of difficulty in adding disinfectant and bacterial growth are solved, and the continuity and sealing performance of disinfection work are achieved, which simplifies operation and reduces safety risks. .
Patent Information
- Application Number
- CN202420907269.7
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-04-25
- Publication Date
- 2025-01-17
- Estimated Expiration
- 2034-04-25
AI Technical Summary
When the disinfectant is exhausted, the disinfection nozzle may stop working, resulting in an increase in the impact of work progress and the risk of bacterial growth. Adding disinfectant requires disassembly of equipment, which is time-consuming and labor-intensive and has safety risks.
A quick disassembly mechanism is designed to remove the limit of the sealing plug by typing the plunger, simplifying the process of adding disinfectant, avoiding the shutdown of the disinfectant nozzle, and ensuring sealing performance through the rubber pad of the sealing mechanism to prevent external bacteria from entering.
The rapid addition of disinfectant is achieved, the continuity and effectiveness of disinfection work is ensured, the operational risks are reduced, and external bacteria are effectively prevented from entering.
Smart Images
Figure CN222364038U_ABST
Abstract
Description
Technical Field
[0001] The utility model relates to the technical field of clean rooms, in particular to an assembled disinfection and aseptic clean room. Background Art
[0002] The assembled sterile cleanroom is a facility specially designed to provide a highly clean environment. It is equipped with a high-efficiency filter system that can effectively remove dust, bacteria, viruses and other tiny particles in the air. These filters usually adopt a multi-layer structure, including primary filters, medium-efficiency filters and high-efficiency filters to ensure the cleanliness of the indoor air. Before entering the cleanroom, both personnel and objects need to undergo strict disinfection to kill potential pathogens.
[0003] In the existing technology, when the disinfectant in the disinfection equipment is exhausted, the disinfection nozzle may stop working, making it impossible to continue the disinfection operation. This will not only affect the progress of the work, but also increase the risk of bacterial growth and spread. In addition, when the staff adds disinfectant to the disinfection equipment, they need to use disassembly tools to disassemble the disinfection equipment, which is not only time-consuming and labor-intensive, but also may pose certain risks to the safety of the operator. Therefore, we provide an assembled disinfection sterile clean room. Utility Model Content
[0004] The purpose of the utility model is to solve the shortcomings of the prior art and provide an assembled sterile clean room.
[0005] In order to achieve the above-mentioned purpose, the utility model adopts the following technical scheme: an assembled disinfection aseptic clean room, comprising: a quick-release mechanism, the quick-release mechanism comprising a cleaning room body, a disinfection chamber is arranged inside the cleaning room body, disinfection doors are arranged on both sides of the disinfection chamber, a disinfection nozzle is arranged inside the disinfection chamber, escalators are arranged on the other two sides of the disinfection chamber, a disinfection box is arranged on the top of the disinfection chamber, two fixed blocks are arranged on the top of the disinfection box, a shift block is arranged on one side of the two fixed blocks, an adjusting rod is arranged inside the fixed block, a spring is arranged on the outer surface of the adjusting rod, a limiting block is arranged on the end of the adjusting rod away from the shift block, and a sealing mechanism is arranged between the two fixed blocks.
[0006] As a preferred embodiment, the sealing mechanism includes a sealing plug, a limiting groove is provided on a side of the sealing plug close to the limiting block, one end of the limiting block is clamped in the limiting groove, a handle is fixedly connected to the top of the sealing plug, and a rubber pad is fixedly connected to the bottom of the sealing plug.
[0007] As a preferred embodiment, the disinfection door is movably connected to the disinfection chamber via a hinge, and the disinfection nozzle is docked on the inner wall of the disinfection chamber.
[0008] As a preferred embodiment, the escalator is welded to the outside of the disinfection chamber, and the bottom of the disinfection box is fixedly connected to the top of the disinfection chamber.
[0009] As a preferred implementation, one side of the fixing block is fixedly connected to the top of the disinfection box, and the side of the shifting block close to the sealing plug is in contact with the side of the fixing block away from the sealing plug.
[0010] As a preferred implementation, the adjusting rod is movably connected inside the shifting block, and one end of the adjusting rod close to the shifting block passes through the fixed block and the spring and is fixedly connected to one side of the limiting block close to the fixed block.
[0011] As a preferred implementation, one end of the spring is fixedly connected to a side of the inner wall of the fixing block close to the shifting block.
[0012] As a preferred implementation, the other end of the spring is fixedly connected to a side of the limiting block close to the fixed block.
[0013] Compared with the prior art, the advantages and positive effects of the utility model are:
[0014] 1. Through the installed quick-release mechanism, the staff only needs to turn the dial block to release the limit of the sealing plug, and then add disinfectant into the disinfection box, which greatly saves time and human resources, avoids the lack of disinfectant causing the disinfection nozzle to enter the shutdown state, thereby ensuring the continuity and effectiveness of the disinfection work;
[0015] 2. The rubber pad in the installed sealing mechanism has good elasticity and sealing performance, which can effectively prevent external bacteria from entering the disinfection box. BRIEF DESCRIPTION OF THE DRAWINGS
[0016] Figure 1 The utility model provides a structural schematic diagram of an assembled disinfection and aseptic clean room.
[0017] Figure 2 The utility model provides an assembled quick-disassembly structure schematic diagram of a disinfection and aseptic clean room.
[0018] Figure 3 The utility model provides a schematic diagram of the partial unfolding structure of an assembled quick-release mechanism for a sterile clean room.
[0019] Figure 4 The utility model provides a schematic structural diagram of a quick-release mechanism and a sealing mechanism for an assembled sterile clean room.
[0020] Figure 5 The utility model provides a schematic diagram of the partial dissection structure of a quick-disassembly mechanism for an assembled disinfection and aseptic clean room.
[0021] Figure 6 The utility model provides a sealing structure schematic diagram of an assembled sterile clean room.
[0022] Legend:
[0023] 1. Quick release mechanism; 11. Cleaning room body; 12. Disinfection room; 13. Disinfection door; 14. Escalator; 15. Disinfection nozzle; 16. Disinfection box; 17. Fixed block; 18. Dial block; 19. Adjustment rod; 110. Limit block; 111. Spring;
[0024] 2. Sealing mechanism; 21. Sealing plug; 22. Limiting groove; 23. Handle; 24. Rubber pad. DETAILED DESCRIPTION
[0025] The following will be combined with the drawings in the embodiments of the utility model to clearly and completely describe the technical solutions in the embodiments of the utility model. Obviously, the described embodiments are only part of the embodiments of the utility model, not all of the embodiments. Based on the embodiments in 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.
[0026] Example 1
[0027] like Figure 1-Figure 6As shown, the utility model provides a technical solution: an assembled sterile disinfection clean room, comprising: a quick-release mechanism 1, the quick-release mechanism 1 comprises a cleaning room body 11, a disinfection room 12 is arranged inside the cleaning room body 11, disinfection doors 13 are arranged on both sides of the disinfection room 12, the disinfection door 13 is movably connected to the disinfection room 12 through a hinge, a disinfection nozzle 15 is arranged inside the disinfection room 12, the disinfection nozzle 15 is docked on the inner wall of the disinfection room 12, escalators 14 are arranged on the other two sides of the disinfection room 12, the escalator 14 is welded to the outside of the disinfection room 12, a disinfection box 16 is arranged on the top of the disinfection room 12, the bottom of the disinfection box 16 is fixedly connected to the top of the disinfection room 12, and two fixed blocks 17 are arranged on the top of the disinfection box 16, one side of the fixed block 17 is fixed to the top of the disinfection box 16 Connection, a shift block 18 is provided on one side of the two fixed blocks 17, and the side of the shift block 18 close to the sealing plug 21 is in contact with the side of the fixed block 17 away from the sealing plug 21, an adjusting rod 19 is provided inside the fixed block 17, the adjusting rod 19 is movably connected inside the shift block 18, a spring 111 is provided on the outer surface of the adjusting rod 19, a limiting block 110 is provided on the end of the adjusting rod 19 away from the shift block 18, the end of the adjusting rod 19 close to the shift block 18 passes through the fixed block 17 and the spring 111 and is fixedly connected to the side of the limiting block 110 close to the fixed block 17, one end of the spring 111 is fixedly connected to the side of the inner wall of the fixed block 17 close to the shift block 18, and the other end of the spring 111 is fixedly connected to the side of the limiting block 110 close to the fixed block 17, and a sealing mechanism 2 is provided between the two fixed blocks 17.
[0028] In this embodiment, when the staff needs to use the sterile clean room, they can push open the disinfection door 13 to enter the disinfection room 12. In the disinfection room 12, there is a disinfection spray sprayed by the disinfection nozzle 15 to disinfect the staff's whole body. When the disinfection is completed, another disinfection door 13 can be pushed open to enter the cleaning room body 11 to change clothes. However, since the disinfection nozzle 15 sprays disinfection spray for a long time, the disinfectant in the disinfection box 16 needs to be added regularly. Therefore, when the staff needs to add disinfectant to the disinfection box 16, they can use the escalator 14 to climb up the disinfection room 12, and then turn the dial block 18. When the dial block 18 is turned, one side of it will be squeezed and rubbed with the fixed block 17, and then the adjustment rod 19 and the limit block 110 will move toward the dial block 1 8 moves on one side, and at the same time, the spring 111 will be subjected to the extrusion force generated by the movement of the limit block 110, causing the spring 111 to shrink and deform, so that the limit block 110 will be out of the limit groove 22, and the sealing plug 21 will be released. The staff can pull out the sealing plug 21 to add disinfectant to the disinfection box 16. When the disinfectant is added, the sealing plug 21 is placed in the card slot at the top of the disinfection box 16. After the pull block 18 is released, the spring 111 will be released, and then the limit block 110 is pushed into the limit groove 22. Through the installed quick-release mechanism 1, disinfectant can be added to the disinfection box 16 more quickly to avoid the lack of disinfectant causing the disinfection nozzle 15 to enter a shutdown state, thereby ensuring the continuity and effectiveness of the disinfection work.
[0029] Example 2
[0030] like Figure 4 , Figure 6 As shown, the sealing mechanism 2 includes a sealing plug 21, and a limiting groove 22 is opened on one side of the sealing plug 21 close to the limiting block 110. One end of the limiting block 110 is clamped in the limiting groove 22. A handle 23 is fixedly connected to the top of the sealing plug 21, and a rubber pad 24 is fixedly connected to the bottom of the sealing plug 21.
[0031] In this embodiment, a rubber pad 24 is fixedly connected to the bottom of the sealing plug 21. The rubber pad 24 has good elasticity and sealing performance, and can effectively prevent external bacteria from entering the disinfection box 16. After the staff releases the limit on the sealing plug 21, they can pull the handle 23 to remove the sealing plug 21 from the disinfection box 16, and then add disinfectant to the disinfection box 16.
[0032] Working principle:
[0033] like Figure 1-Figure 6As shown, when the staff needs to enter the sterile clean room, they can push open the disinfection door 13 at the entrance. Once entering the disinfection room 12, they will immediately feel the disinfection spray sprayed by the disinfection nozzle 15. These sprays will fully cover the body of the staff to ensure that they are thoroughly disinfected before entering the clean room. After completing the disinfection process, the staff can continue to push open another disinfection door 13 and enter the clean room body 11 to change clothes. If the staff needs to add disinfectant to the disinfection box 16, they can use the escalator 14 to climb up to the upper part of the disinfection room 12, find the dial block 18 and gently push it. When the dial block 18 is pushed, one side of it will be squeezed and rubbed with the fixed block 17. This friction will cause the adjusting rod 19 and the limit block 110 to move toward the side of the dial block 18. At the same time, the spring The spring 111 will be subjected to the extrusion force generated by the movement of the limit block 110, and this extrusion force will cause the spring 111 to contract and deform. As the spring 111 contracts, the limit block 110 will disengage from the limit groove 22, and the sealing plug 21 will also be released from the limit. The staff can grab the handle 23 and then easily remove the sealing plug 21 from the disinfection box 16, so that the required disinfectant can be poured into the disinfection box 16. Once the disinfectant is added, the staff only needs to refill the sealing plug 21 into the card slot at the top of the disinfection box 16. Finally, the staff releases the dial block 18, and the spring 111 will be released. As the spring 111 is released, the limit block 110 will be pushed and stuck into the limit groove 22. This process ensures the sealing inside the disinfection box 16 and prevents any external contaminants from entering.
[0034] The above description is only a preferred embodiment of the present invention and does not limit the present invention in other forms. Any technician familiar with the profession may use the technical content disclosed above to change or modify it into an equivalent embodiment with equivalent changes and apply it to other fields. However, any simple modification, equivalent change and modification made to the above embodiment based on the technical essence of the present invention without departing from the content of the technical solution of the present invention still falls within the protection scope of the technical solution of the present invention.
Claims
1. An assembled sterile clean room, characterized in that: include: A quick release mechanism (1) comprises a cleaning chamber body (11), a disinfection chamber (12) is arranged inside the cleaning chamber body (11), disinfection doors (13) are arranged on both sides of the disinfection chamber (12), a disinfection nozzle (15) is arranged inside the disinfection chamber (12), escalators (14) are arranged on the other two sides of the disinfection chamber (12), a disinfection box (16) is arranged on the top of the disinfection chamber (12), two fixed blocks (17) are arranged on the top of the disinfection box (16), a shifting block (18) is arranged on one side of the two fixed blocks (17), an adjusting rod (19) is arranged inside the fixed block (17), a spring (111) is arranged on the outer surface of the adjusting rod (19), a limiting block (110) is arranged on the end of the adjusting rod (19) away from the shifting block (18), and a sealing mechanism (2) is arranged between the two fixed blocks (17).
2. The assembled sterile clean room according to claim 1, characterized in that: The sealing mechanism (2) comprises a sealing plug (21), a limiting groove (22) being provided on a side of the sealing plug (21) close to the limiting block (110), one end of the limiting block (110) being clamped in the limiting groove (22), a handle (23) being fixedly connected to the top of the sealing plug (21), and a rubber pad (24) being fixedly connected to the bottom of the sealing plug (21).
3. The assembled sterile clean room according to claim 2, characterized in that: The disinfection door (13) is movably connected to the disinfection chamber (12) via a hinge, and the disinfection nozzle (15) is docked on the inner wall of the disinfection chamber (12).
4. The assembled sterile clean room according to claim 1, characterized in that: The escalator (14) is welded to the outside of the disinfection chamber (12), and the bottom of the disinfection box (16) is fixedly connected to the top of the disinfection chamber (12).
5. The assembled sterile clean room according to claim 1, characterized in that: One side of the fixing block (17) is fixedly connected to the top of the disinfection box (16), and the side of the shifting block (18) close to the sealing plug (21) is in contact with the side of the fixing block (17) away from the sealing plug (21).
6. The assembled sterile clean room according to claim 1, characterized in that: The adjusting rod (19) is movably connected inside the shifting block (18); one end of the adjusting rod (19) close to the shifting block (18) passes through the fixed block (17) and the spring (111) and is fixedly connected to one side of the limiting block (110) close to the fixed block (17).
7. The assembled sterile clean room according to claim 1, characterized in that: One end of the spring (111) is fixedly connected to a side of the inner wall of the fixing block (17) close to the shifting block (18).
8. The assembled sterile clean room according to claim 1, characterized in that: The other end of the spring (111) is fixedly connected to a side of the limiting block (110) close to the fixing block (17).