Sensitive skin cream adaptability testing device
By introducing a combination of dustproof net, blower and activated carbon plate into the cream testing device, the problem of iodine vapor stimulating health is solved, and the effective filtration and safe use of iodine vapor are achieved.
Patent Information
- Application Number
- CN202421291392.7
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-06-07
- Publication Date
- 2025-07-22
- Estimated Expiration
- 2034-06-07
AI Technical Summary
The existing cream testing device does not have a structure to purify iodine steam, which stimulates the eyes and nose and damages the health of the body.
In the test device, dustproof net, air blower, activated carbon plate and gas sensor are installed, and iodine vapor is filtered through the airflow, and an activated carbon plate is used to absorb iodine vapor, and a warning light is set to remind you to replace the activated carbon plate.
Effectively filter iodine vapor to avoid users from being exposed to toxic iodine vapor, ensure health, and replace activated carbon plates with convenient and safe conditions.
Smart Images

Figure CN223139510U_ABST
Abstract
Description
Technical Field
[0001] The utility model relates to a testing device, in particular to a testing device for the adaptability of facial cream for sensitive skin, belonging to the technical field of skin care product experimental equipment. Background Technique
[0002] Facial cream refers to a chemical industrial product applied to the human face, which plays the roles of cleaning, whitening, antioxidant, moisturizing, and water retention. The facial cream moisturizes sensitive skin through the water phase in the ingredients and then keeps it moist through the oil phase in the ingredients. Dry skin is suitable for using facial cream and relatively moisturizing lotion, while oily and combination skin is suitable for refreshing lotion and oil-free facial cream. In dry seasons, such as autumn and winter, facial cream with a thicker texture is suitable, while in hot seasons, such as spring and summer, refreshing lotion is suitable. Iodine tincture is used when detecting the antioxidant property of facial cream, and the iodine vapor released by the evaporation of iodine tincture is toxic.
[0003] Among them, the "facial cream testing device" disclosed in the application number "CN202321952237.0" "comprises a mounting base, a plurality of support frames are arranged on the mounting base, a combustion table is arranged inside the mounting base, a working bottle is arranged on the plurality of support frames, a fixing cylinder is arranged on the working bottle, a fixing plate is arranged on the top end face of the fixing cylinder, a plurality of support rods are uniformly arranged on the fixing plate, and a top plate is arranged on the top end faces of the plurality of support rods. A driving motor is arranged on the top plate, the driving end of the driving motor penetrates through the top plate, and a rotating rod is arranged on the driving end of the driving motor. A stirring frame is arranged on the bottom end face of the rotating rod; the bottom of the working bottle is communicated with a discharge pipe, and a control valve is arranged on the discharge pipe. The utility model is provided with a working bottle for testing the antioxidant property, PH test and fire test method of facial cream, and integrating multiple test items to improve the detection efficiency".
[0004] However, the above method still has the following defects: there is no structure for purifying iodine vapor, and the residual iodine tincture in the working bottle generates iodine vapor after heating, which will severely irritate the eyes and nose and damage physical health. Content of the Utility Model
[0005] The purpose of the utility model is to provide a testing device for the adaptability of facial cream for sensitive skin, so as to solve the problem that the existing structure does not purify iodine vapor and iodine vapor damages physical health.
[0006] To achieve the above object, the present utility model provides the following technical solutions: a sensitive skin cream adaptability testing device, including a testing box, a base is provided at the bottom end of the testing box, an air blowing pipe is provided on the inner wall of the base, a dust-proof net and an air blowing fan are respectively provided on the inner wall of the air blowing pipe, a medicine application component and an adjustment component are respectively provided inside the testing box, an air outlet pipe is provided on the back of the testing box, a first gas sensor module, two first rubber frames and two second rubber frames are respectively provided on the inner wall of the air outlet pipe, two activated carbon plates are slidably connected to the inner wall of the air outlet pipe, two positioning grooves are opened at the top end of the air outlet pipe, and two sealing plates are provided at the top end of the air outlet pipe by screws.
[0007] As a preferred technical solution of the present utility model, limiting grooves engaged with the activated carbon plates are opened at the bottom ends of the two sealing plates, handles are provided at the top ends of the two sealing plates, the inner walls of the two positioning grooves are respectively slidably connected to the surfaces of the two activated carbon plates, one side of one of the activated carbon plates is slidably connected to one side of one of the first rubber frames, the other side of one of the activated carbon plates is slidably connected to one side of one of the second rubber frames, one side of the other activated carbon plate is slidably connected to one side of the other first rubber frame, the other side of the other activated carbon plate is slidably connected to one side of the other second rubber frame, the two second rubber frames and the two first rubber frames are both made of silicone rubber material, and the first gas sensor module is disposed between the two activated carbon plates.
[0008] As a preferred technical solution of the present utility model, the medicine application component includes a medicine storage box and a stirring component, the medicine storage box is provided at the top end of the testing box, a first observation window is provided on the surface of the medicine storage box, a medicine outlet pipe is provided on the front of the medicine storage box, one end of the medicine outlet pipe penetrates through the top end of the testing box and is disposed inside the top of the testing box, a medicine supplement pipe is provided on one side of the medicine storage box, and electric valves are respectively provided on the surfaces of the medicine supplement pipe and the medicine outlet pipe.
[0009] As a preferred technical solution of the present utility model, the stirring component includes a connection seat and a stirring motor, the connection seat is provided on the inner wall of the top end of the testing box, the connection seat is sleeved outside the bottom of the medicine outlet pipe, a transmission pipe is rotatably connected to the inner wall of the connection seat through a sealing bearing, the inner wall of the transmission pipe is slidably connected to the surface of the medicine outlet pipe, stirring blades are provided on the surface of the transmission pipe, the stirring motor is provided at the top end of the testing box, a driving gear is provided on the transmission shaft of the stirring motor, and a gear ring is meshed and connected to one side of the driving gear, and the inner wall of the gear ring is connected to the surface of the top of the transmission pipe.
[0010] As a preferred technical solution of the present utility model, the adjusting assembly includes a lifting motor and two guiding boxes. The lifting motor is arranged on one side of the top end of the test box. The lifting motor is a forward and reverse motor. Both of the two guiding boxes are arranged on the inner wall of the test box. The inner walls of both of the two guiding boxes are slidably connected with lifting frames. There is a lifting table between the two lifting frames. A container groove is opened at the top end of the lifting table. A sample container is slidably connected to the inner wall of the container groove. One of the inner walls of the guiding boxes is rotatably connected with a transmission lead screw through a bearing. One end of the transmission lead screw is connected to the transmission shaft of the lifting motor. The contact part between the transmission lead screw and one of the lifting frames is threadedly connected through a lead screw nut.
[0011] As a preferred technical solution of the present utility model, the sample container is sleeved outside the stirring blade. A hemispherical heating block is arranged at the bottom of the lifting table. The lifting table and the heating block are arranged as an integrated structure. The lifting table, the heating block and the sample container are all made of brass material.
[0012] As a preferred technical solution of the present utility model, a combustion table is arranged on the inner wall of the bottom end of the test box. The gas supply pipe of the combustion table penetrates through the inner wall of the test box and is placed outside the test box. A second gas sensor module is arranged on the inner wall of the top end of the test box. A power collection box, a second observation window and a third observation window are respectively arranged on the front surface of the test box. A sealed box door is hinged on the front surface of the test box. A handle and a fourth observation window are respectively arranged on the front surface of the sealed box door.
[0013] As a preferred technical solution of the present utility model, a single-chip microcomputer is arranged inside the power collection box. A first warning lamp and a second warning lamp are respectively arranged on one side of the power collection box. The first warning lamp, the second warning lamp, the first gas sensor module and the second gas sensor module are all electrically connected to the single-chip microcomputer. A switch panel is arranged on the front surface of the power collection box.
[0014] Compared with the related technology, the sensitive skin cream adaptability testing device provided by the present utility model has the following beneficial effects:
[0015] The blowing fan generates air flow. The air flow sequentially passes through the dust-proof net and the blowing pipe and enters the inside of the test box. Heating the iodine solution generates iodine vapor. The air flow and the iodine vapor enter the air outlet pipe. The two activated carbon plates adsorb the iodine vapor in the air flow, realizing the filtration of iodine vapor and avoiding the user from contacting the toxic iodine vapor, which is safer.
[0016] Remove the screw and pull up the sealing plate through the handle, so that the sealing plate is separated from the air outlet pipe. Pull out the activated carbon plate upward. Slide the new activated carbon plate into the positioning groove. The second rubber frame and the first rubber frame seal the gap between the activated carbon plate and the air outlet pipe. Then move the sealing plate downward and screw in the screw to fix the sealing plate, completing the replacement of the activated carbon plate, which is very convenient.
[0017] When the first gas sensor module detects iodine vapor, the single-chip microcomputer will activate the first warning light, and the first warning light will light up to remind the user that there is iodine vapor in the space separated by two activated carbon plates. That is to say, the filtering effect of the activated carbon plate close to the test box becomes poor and needs to be replaced in time;
[0018] When the second gas sensor module detects iodine vapor, the single-chip microcomputer will activate the second warning light, and the second warning light will light up to remind the user that there is iodine vapor inside the test box and not to open the sealed box door, which is beneficial to maintaining the user's physical health. BRIEF DESCRIPTION OF THE DRAWINGS
[0019] Figure 1 is a schematic structural diagram of the present utility model;
[0020] Figure 2 For the present utility model Figure 1 an enlarged structural diagram of part A
[0021] Figure 3 is a schematic sectional structural diagram of the present utility model;
[0022] Figure 4 is a schematic side sectional structural diagram of the present utility model;
[0023] Figure 5 For the present utility model Figure 4 an enlarged structural diagram of part B;
[0024] Figure 6 is a schematic structural diagram of the medicine application component of the present utility model.
[0025] In the figure: 1. Test box; 2. Base; 3. Blowing pipe; 4. Dust-proof net; 5. Medicine application component; 51. Medicine storage box; 52. First observation window; 53. Medicine outlet pipe; 54. Medicine replenishing pipe; 6. Adjustment component; 61. Lifting motor; 62. Guide box; 63. Lifting frame; 64. Lifting table; 65. Container groove; 66. Sample container; 67. Transmission lead screw; 7. Stirring component; 71. Connecting seat; 72. Stirring motor; 73. Transmission pipe; 74. Stirring blade; 75. Driving gear; 76. Ring gear; 8. Air outlet pipe; 9. First rubber frame; 10. Second rubber frame; 11. Activated carbon plate; 12. Positioning groove; 13. Sealing plate; 14. Handle; 15. First gas sensor module; 16. Second gas sensor module; 17. Power distribution box; 18. Second observation window; 19. Third observation window; 20. Sealed box door; 21. Handle; 22. Fourth observation window; 23. First warning light; 24. Second warning light; 25. Switch panel; 26. Combustion table. DETAILED DESCRIPTION OF THE EMBODIMENTS
[0026] The technical solutions in the embodiments of the present utility model will be clearly and completely described below with reference to the accompanying drawings in the embodiments of the present utility model. Obviously, the described embodiments are only a part of the embodiments of the present utility model, rather than all the embodiments. All other embodiments obtained by those of ordinary skill in the art based on the embodiments of the present utility model without creative efforts shall fall within the protection scope of the present utility model.
[0027] Please refer to Figures 1-6 , the present utility model provides a sensitive skin cream adaptability testing device, including a testing box 1. A base 2 is fixedly provided at the bottom end of the testing box 1. An air blowing pipe 3 is fixedly provided on the inner wall of the base 2. There are four air blowing pipes 3. A dust-proof net 4 and an air blowing fan are respectively fixedly provided on the inner walls of the air blowing pipes 3. A medicine application component 5 and an adjustment component 6 are respectively provided inside the testing box 1. An air outlet pipe 8 is fixedly provided on the back of the testing box 1. A first gas sensor module 15, two first rubber frames 9 and two second rubber frames 10 are respectively fixedly provided on the inner wall of the air outlet pipe 8. Two activated carbon plates 11 are slidably connected to the inner wall of the air outlet pipe 8. Two positioning grooves 12 are opened at the top end of the air outlet pipe 8. Two sealing plates 13 are fixedly provided at the top end of the air outlet pipe 8 by screws. When the air blowing fan is started, the air blowing fan generates an air flow. The air flow sequentially passes through the dust-proof net 4 and the air blowing pipe 3 and enters the inside of the testing box 1. The heated residual iodine solution will generate iodine vapor. The air flow and the iodine vapor enter the air outlet pipe 8. The two activated carbon plates 11 will adsorb the iodine vapor in the air flow to achieve filtration, avoiding the user from contacting the toxic iodine vapor and being safer.
[0028] The bottom ends of the two sealing plates 13 are provided with limiting grooves engaged with the activated carbon plates 11, and the tops of the two sealing plates 13 are fixed with handles 14. The inner walls of the two positioning grooves 12 are slidably connected to the surfaces of the two activated carbon plates 11 respectively, one side of one of the activated carbon plates 11 is slidably connected to one side of one of the first rubber frames 9, the other side of one of the activated carbon plates 11 is slidably connected to one side of one of the second rubber frames 10, one side of the other activated carbon plate 11 is slidably connected to one side of the other first rubber frame 9, and the other side of the other activated carbon plate 11 is slidably connected to one side of the other second rubber frame 10. The two second rubber frames 10 and the two first rubber frames 9 are all Made of silicone rubber material, the first gas sensor module 15 is placed between the two activated carbon plates 11, and the activated carbon plate 11 is slid into the interior of the positioning groove 12 until the activated carbon plate 11 is pressed against the inner wall of the bottom end of the outlet pipe 8. At this time, the second rubber frame 10 and the first rubber frame 9 are close to the activated carbon plate 11 to seal the gap between the activated carbon plate 11 and the outlet pipe 8. Then the sealing plate 13 is moved downward to make the activated carbon plate 11 engage with the limiting groove to complete the positioning of the sealing plate 13, and then the screws are screwed in to fix the sealing plate 13 to complete the installation of the activated carbon plate 11. The silicone rubber material has excellent heat resistance and corrosion resistance, which prolongs the service life of the second rubber frame 10 and the first rubber frame 9.
[0029] The medicine applying component 5 includes a medicine storage box 51 and a stirring component 7. The medicine storage box 51 is fixedly arranged on the top of the test box 1. A first observation window 52 is fixedly arranged on the surface of the medicine storage box 51. A medicine outlet pipe 53 is fixedly arranged on the front of the medicine storage box 51. One end of the medicine outlet pipe 53 passes through the top of the test box 1 and is placed inside the top of the test box 1. A medicine replenishing pipe 54 is fixedly arranged on one side of the medicine storage box 51. Electric valves are fixedly arranged on the surfaces of the medicine replenishing pipe 54 and the surfaces of the medicine outlet pipe 53. A proper amount of iodine is added to the inside of the medicine storage box 51 through the medicine replenishing pipe 54. Whether there is iodine solution in the medicine storage box 51 is observed through the first observation window 52. A proper amount of iodine solution is added to the inside of the sample container 66 through the medicine outlet pipe 53. Furthermore, the medicine outlet pipe 53 can be made of transparent hard plastic to facilitate the observation of the discharge of the reddish-brown iodine solution.
[0030] The stirring assembly 7 includes a connecting seat 71 and a stirring motor 72. The connecting seat 71 is fixedly arranged on the inner wall of the top end of the test box 1. The connecting seat 71 is sleeved on the outside of the bottom of the medicine outlet pipe 53. The inner wall of the connecting seat 71 is rotationally connected with a transmission pipe 73 through a sealed bearing. The inner wall of the transmission pipe 73 is slidably connected with the surface of the medicine outlet pipe 53. The surface of the transmission pipe 73 is fixedly provided with stirring blades 74. There are six stirring blades 74 and they are evenly distributed in a ring shape. The stirring motor 72 is fixedly arranged on the top end of the test box 1. The transmission shaft of the stirring motor 72 is fixedly provided with a driving gear 75. One side of the driving gear 75 is meshed and connected with a gear ring 76. The inner wall of the gear ring 76 is fixedly connected with the surface of the top of the transmission pipe 73. When the stirring motor 72 is started, the stirring motor 72 will drive the driving gear 75 to rotate. The driving gear 75 drives the gear ring 76 to rotate. The gear ring 76 will drive the transmission pipe 73 to rotate. The transmission pipe 73 drives the stirring blades 74 to rotate. The stirring blades 74 will stir the iodine solution (mixed with iodine and water in a certain ratio) and the cream sample inside the sample container 66 to obtain a mixed solution.
[0031] The adjusting assembly 6 includes a lifting motor 61 and two guiding boxes 62. The lifting motor 61 is fixedly arranged on one side of the top end of the test box 1. The lifting motor 61 is a forward and reverse rotation motor. Both of the two guiding boxes 62 are fixedly arranged on the inner wall of the test box 1. The inner walls of both of the two guiding boxes 62 are slidably connected with a lifting frame 63. A lifting table 64 is fixedly arranged between the two lifting frames 63. A container groove 65 is opened at the top end of the lifting table 64. The inner wall of the container groove 65 is slidably connected with a sample container 66. The inner wall of one of the guiding boxes 62 is rotationally connected with a transmission lead screw 67 through a bearing. One end of the transmission lead screw 67 is fixedly connected with the transmission shaft of the lifting motor 61. The contact part between the transmission lead screw 67 and one of the lifting frames 63 is threadedly connected through a lead screw nut. First, add the cream sample into the sample container 66, and then move the sample container 66 to make the sample container 66 extend into the middle of the inside of the test box 1 and be stuck in the container groove 65.
[0032] The sample container 66 is sleeved on the outside of the stirring blades 74. A hemispherical heating block is fixedly arranged at the bottom of the lifting table 64. The lifting table 64 and the heating block are of an integrated structure. The lifting table 64, the heating block and the sample container 66 are all made of brass material. The hemispherical shape is beneficial for the flame of the combustion table 26 to heat the lifting table 64. The mixed solution inside the sample container 66 is heated through the heat-conducting lifting table 64 and the sample container 66 until the mixed solution boils. If it becomes milky after boiling and has a strong and fragrant smell, it indicates that this product is safe. If there is a smoking phenomenon after boiling and pungent residues are generated, it indicates that the mineral oil in the product exceeds the standard or it is filled with boride, and it may cause harm to the skin after use.
[0033] The inner wall at the bottom of the test chamber 1 is fixedly provided with a combustion table 26. The gas supply pipe of the combustion table 26 penetrates through the inner wall of the test chamber 1 and is placed outside the test chamber 1. The inner wall at the top of the test chamber 1 is fixedly provided with a second gas sensor module 16. The front of the test chamber 1 is fixedly provided with a current collector box 17, a second observation window 18 and a third observation window 19 respectively. The front of the test chamber 1 is hinged with a sealed chamber door 20. The front of the sealed chamber door 20 is fixedly provided with a handle 21 and a fourth observation window 22 respectively. Gas is supplied to the combustion table 26 through the gas supply pipe. The second observation window 18, the third observation window 19 and the fourth observation window 22 are provided for observing the position of the sample container 66.
[0034] A single-chip microcomputer is fixedly installed inside the current collector box 17. A first warning light 23 and a second warning light 24 are fixedly provided on one side of the current collector box 17 respectively. The first warning light 23, the second warning light 24, the first gas sensor module 15 and the second gas sensor module 16 are all electrically connected to the single-chip microcomputer. A switch panel 25 is provided on the front of the current collector box 17. If the antioxidant property of the facial cream is poor, then iodine tincture will remain in the mixed solution. The iodine tincture generates iodine vapor after heating. The first gas sensor module 15 and the second gas sensor module 16 can detect the concentration of the iodine vapor and transmit it to the single-chip microcomputer. A program is set inside the single-chip microcomputer. When the first gas sensor module 15 detects iodine vapor, the measured transmission value is greater than 0, and the single-chip microcomputer will activate the first warning light 23, and the first warning light 23 will light up to remind the user that there is iodine vapor in the space separated by the two activated carbon plates 11. That is to say, the filtering effect of the activated carbon plate 11 close to the test chamber 1 becomes poor and needs to be replaced in time. Further, after replacing the activated carbon plate 11 close to the test chamber 1 multiple times, the activated carbon plate 11 far from the test chamber 1 can be disassembled and installed in the positioning groove 12 close to the test chamber 1, and then a brand-new activated carbon plate 11 is inserted into the positioning groove 12 far from the test chamber 1 to prevent the iodine vapor in the space separated by the two activated carbon plates 11 from flowing into the room due to the poor filtering effect of the activated carbon plate 11 far from the test chamber 1 after long-term use. When the second gas sensor module 16 detects iodine vapor, the measured transmission value is greater than 0, and the single-chip microcomputer will activate the second warning light 24, and the second warning light 24 will light up to remind the user that there is iodine vapor inside the test chamber 1 and not to open the sealed chamber door 20, which is beneficial to maintaining the health of the user.
[0035] During use, four blowing fans are started through the switch panel 25. The blowing fans will generate airflows. The airflows sequentially pass through the dust-proof net 4 and the blow pipes 3 and enter the inside of the test chamber 1. Heating the iodine solution will generate iodine vapor. The airflows and the iodine vapor enter the air outlet pipe 8. The two activated carbon plates 11 adsorb the iodine vapor in the airflows to achieve iodine vapor filtration, avoiding the user from contacting the toxic iodine vapor and being safer.
[0036] When the activated carbon plate 11 needs to be replaced, remove the screws and pull the sealing plate 13 upward through the handle 14 to make the sealing plate 13 disengage from the air outlet pipe 8. Then, pull out the activated carbon plate 11 upward, slide the new activated carbon plate 11 into the positioning groove 12. When the activated carbon plate 11 moves downward, it squeezes the second rubber frame 10 and the first rubber frame 9, causing the second rubber frame 10 and the first rubber frame 9 to deform and closely adhere to the activated carbon plate 11. The second rubber frame 10 and the first rubber frame 9 seal the gap between the activated carbon plate 11 and the air outlet pipe 8. Then, move the sealing plate 13 downward to make the activated carbon plate 11 engage with the limit groove. Finally, screw in the screws to fix the sealing plate 13, completing the replacement of the activated carbon plate 11, which is very convenient. The silicone rubber material has excellent heat resistance and corrosion resistance, extending the service life of the second rubber frame 10 and the first rubber frame 9;
[0037] It should be emphasized that when testing the adaptability (antioxidant property) of the facial cream, first add the facial cream sample into the interior of the sample container 66, move the sample container 66 to make the sample container 66 extend into the middle inside the test box 1 and snap into the container slot 65. Then, start the lifting motor 61 through the switch panel 25. The lifting motor 61 drives the transmission lead screw 67 to rotate, and the transmission lead screw 67 drives the lifting frame 63, the lifting platform 64, and the sample container 66 to move upward, making the sample container 66 sleeved outside the stirring blade 74. Then, open the electric valve corresponding to the medicine outlet pipe 53 through the switch panel 25, and add an appropriate amount of iodine solution into the interior of the sample container 66 through the medicine outlet pipe 53. Start the stirring motor 72. The stirring motor 72 drives the driving gear 75 to rotate, the driving gear 75 drives the gear ring 76 to rotate, the gear ring 76 drives the transmission pipe 73 to rotate, and the transmission pipe 73 drives the stirring blade 74 to rotate. The stirring blade 74 stirs the iodine solution and the facial cream sample inside the sample container 66. After sufficient stirring, a mixed solution is obtained. If the mixed solution returns to a transparent state, it indicates that the facial cream has an antioxidant effect. If the mixed solution cannot be restored or even turns black, it indicates that the facial cream has no antioxidant function and may even exacerbate the oxidative aging of the skin.
[0038] Although the embodiments of the present invention have been shown and described, for those of ordinary skill in the art, it can be understood that various changes, modifications, substitutions, and variations can be made to these embodiments without departing from the principle and spirit of the present invention. The scope of the present invention is defined by the appended claims and their equivalents.
Claims
1. Sensitive skin cream adaptability testing device, including a test chamber (1), characterized in that, The bottom end of the test chamber (1) is provided with a base (2). The inner wall of the base (2) is provided with an air blowing pipe (3). The inner walls of the air blowing pipe (3) are respectively provided with a dust-proof net (4) and an air blowing fan. The interior of the test chamber (1) is respectively provided with a medicine feeding assembly (5) and an adjusting assembly (6). The back of the test chamber (1) is provided with an air outlet pipe (8). The inner walls of the air outlet pipe (8) are respectively provided with a first gas sensor module (15), two first rubber frames (9) and two second rubber frames (10). Two activated carbon plates (11) are slidably connected to the inner wall of the air outlet pipe (8). Two positioning grooves (12) are opened at the top end of the air outlet pipe (8). Two sealing plates (13) are provided at the top end of the air outlet pipe (8) by screws.
2. The sensitive skin cream adaptability testing device according to claim 1, characterized in that: The bottom ends of the two sealing plates (13) are both provided with limiting grooves that are engaged with the activated carbon plates (11). The top ends of the two sealing plates (13) are both provided with handles (14). The inner walls of the two positioning grooves (12) are respectively slidably connected to the surfaces of the two activated carbon plates (11). One side of one of the activated carbon plates (11) is slidably connected to one side of one of the first rubber frames (9). The other side of one of the activated carbon plates (11) is slidably connected to one side of one of the second rubber frames (10). One side of the other activated carbon plate (11) is slidably connected to one side of the other first rubber frame (9). The other side of the other activated carbon plate (11) is slidably connected to one side of the other second rubber frame (10). The two second rubber frames (10) and the two first rubber frames (9) are both made of silicone rubber material. The first gas sensor module (15) is placed between the two activated carbon plates (11).
3. The sensitive skin cream adaptability testing device according to claim 1, characterized in that: The medicine feeding assembly (5) includes a medicine storage box (51) and a stirring assembly (7). The medicine storage box (51) is arranged at the top end of the test chamber (1). The surface of the medicine storage box (51) is provided with a first observation window (52). The front of the medicine storage box (51) is provided with a medicine outlet pipe (53). One end of the medicine outlet pipe (53) penetrates through the top end of the test chamber (1) and is placed inside the top of the test chamber (1). One side of the medicine storage box (51) is provided with a medicine replenishing pipe (54). Electric valves are arranged on the surfaces of both the medicine replenishing pipe (54) and the medicine outlet pipe (53).
4. The sensitive skin cream adaptability testing device according to claim 3, characterized in that: The stirring assembly (7) includes a connecting seat (71) and a stirring motor (72). The connecting seat (71) is arranged on the inner wall of the top end of the test chamber (1). The connecting seat (71) is sleeved outside the bottom of the medicine outlet pipe (53). The inner wall of the connecting seat (71) is rotatably connected with a transmission pipe (73) through a sealed bearing. The inner wall of the transmission pipe (73) is slidably connected to the surface of the medicine outlet pipe (53). Stirring blades (74) are arranged on the surface of the transmission pipe (73). The stirring motor (72) is arranged at the top end of the test chamber (1). A driving gear (75) is arranged on the transmission shaft of the stirring motor (72). One side of the driving gear (75) is meshed with a toothed ring (76). The inner wall of the toothed ring (76) is connected to the surface of the top of the transmission pipe (73).
5. The sensitive skin cream adaptability testing device according to claim 4, characterized in that: The adjustment assembly (6) includes a lifting motor (61) and two guide boxes (62). The lifting motor (61) is arranged on one side of the top of the test box (1). The lifting motor (61) is a forward and reverse motor. Both of the two guide boxes (62) are arranged on the inner wall of the test box (1). A lifting frame (63) is slidably connected to the inner wall of each of the two guide boxes (62). A lifting table (64) is arranged between the two lifting frames (63). A container groove (65) is formed in the top end of the lifting table (64). A sample container (66) is slidably connected to the inner wall of the container groove (65). One end of a transmission lead screw (67) is rotatably connected to the inner wall of one of the guide boxes (62) through a bearing. One end of the transmission lead screw (67) is connected to the transmission shaft of the lifting motor (61). The contact part of the transmission lead screw (67) and one of the lifting frames (63) is threadedly connected through a lead screw nut.
6. The sensitive skin cream adaptability testing device according to claim 5, characterized in that: The sample container (66) is sleeved outside the stirring blade (74). A hemispherical heating block is arranged at the bottom of the lifting table (64). The lifting table (64) and the heating block are integrally structured. The lifting table (64), the heating block and the sample container (66) are all made of brass material.
7. The sensitive skin cream adaptability testing device according to claim 1, characterized in that: A combustion table (26) is arranged on the inner wall of the bottom end of the test box (1). The gas supply pipe of the combustion table (26) penetrates through the inner wall of the test box (1) and is located outside the test box (1). A second gas sensor module (16) is arranged on the inner wall of the top end of the test box (1). A power collection box (17), a second observation window (18) and a third observation window (19) are respectively arranged on the front surface of the test box (1). A sealed box door (20) is hinged on the front surface of the test box (1). A handle (21) and a fourth observation window (22) are respectively arranged on the front surface of the sealed box door (20).
8. The sensitive skin cream adaptability testing device according to claim 7, characterized in that: A single-chip microcomputer is arranged inside the power collection box (17). A first warning lamp (23) and a second warning lamp (24) are respectively arranged on one side of the power collection box (17). The first warning lamp (23), the second warning lamp (24), the first gas sensor module (15) and the second gas sensor module (16) are all electrically connected to the single-chip microcomputer. A switch panel (25) is arranged on the front surface of the power collection box (17).
Citation Information
Patent Citations
Facial cream testing device
CN220419279U