CN113252675B - Tobacco germ solution mixing microscopic device and control method thereof - Google Patents
Tobacco germ solution mixing microscopic device and control method thereof Download PDFInfo
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- CN113252675B CN113252675B CN202110766874.8A CN202110766874A CN113252675B CN 113252675 B CN113252675 B CN 113252675B CN 202110766874 A CN202110766874 A CN 202110766874A CN 113252675 B CN113252675 B CN 113252675B
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/84—Systems specially adapted for particular applications
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M27/00—Means for mixing, agitating or circulating fluids in the vessel
- C12M27/02—Stirrer or mobile mixing elements
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M41/00—Means for regulation, monitoring, measurement or control, e.g. flow regulation
- C12M41/12—Means for regulation, monitoring, measurement or control, e.g. flow regulation of temperature
- C12M41/18—Heat exchange systems, e.g. heat jackets or outer envelopes
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
- G01N1/38—Diluting, dispersing or mixing samples
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/01—Arrangements or apparatus for facilitating the optical investigation
Abstract
The invention relates to a tobacco germ solution mixing microscopic device and a control method thereof, wherein the tobacco germ solution mixing microscopic device comprises: the mixing mechanism and the micro-mechanism mixing mechanism comprise a plurality of liquid storage tanks at the top, a mixer is arranged at the lower side of the liquid storage tanks, a shunt assembly is arranged at the bottom of the mixer, a collecting part is connected at the bottom of the shunt assembly, the shunt assembly comprises a plurality of transfer mechanisms, one side of each transfer mechanism is connected with a first shunt passage through a first articulated element, the other side of each transfer mechanism is connected with a second shunt passage through a second articulated element, each transfer mechanism can swing, the mixing mechanism is connected with a micro-mechanism in a matching way, each micro-mechanism comprises an observation platform and a microscope, a solution cavity is arranged at the top of the observation platform, a return tank is arranged at the top of the observation platform and communicated with the solution cavity, germ solution in the mixer circulates through the solution cavity, the germ solution in the solution cavity can be observed in real time through a microscope, and the bacterial wilt can be effectively controlled according to the observation result.
Description
Technical Field
The invention relates to the field of tobacco germ observation and analysis, in particular to a tobacco germ solution mixing microscopic device and a control method thereof.
Background
The tobacco bacterial wilt is also called as myxopathy, tobacco plague and loblolly, and is a disease which is caused by the infection of ralstonia solanacearum and occurs on tobacco. The tobacco bacterial wilt is a typical vascular bundle disease, roots, stems and leaves can be damaged, the most typical symptoms are withering, high temperature places, when the seedbed is watered more or the soil water content is high, the cat ear period (5-6 true leaves) of the tobacco seedling is obviously attacked, and the tobacco seedling is killed in large scale when the seedling is mature. However, in most areas, the temperature is relatively low in the seedling raising stage, and symptoms are not shown even though infection occurs, so that the disease is mainly caused in field tobacco plants. The disease incidence in the field generally has symptoms in a colony stage, the disease peak is reached in a vigorous growing period, the fuming grass bacterial wilt can be continued until the disease condition in a mature stage is a vascular bundle disease caused by Laurella species of the Solanaceae, the early stage is difficult to be perceived by naked eyes, once the wilting symptom exists, the drug control has no effect, the detection of tobacco roots with bacteria and without the disease is enhanced, the advanced control is critical, the ralstonia solanacearum solution is mixed and heated, the temperature is controlled in a proper range, and the ralstonia solanacearum solutions with different concentrations or different batches are fully mixed through a mixing device, so that the ralstonia solanacearum solution can be accurately monitored and analyzed, and the ralstonia solanacearum is treated according to the analysis result of the ralstonia solanacearum solution.
Traditional germ solution is at the mixing process, does not through setting up transfer mechanism, and transfer mechanism can't realize the swing through the articulated elements, can't rock the germ solution in the transfer mechanism, and the mixing effect is relatively poor, and traditional mixing arrangement is carrying out germ solution mixing process in addition, and unable real-time supervision mixing result causes the sample after mixing easily to lose analytical value, is difficult to form the treatment of bacterial wilt pertinence according to the analysis result.
Disclosure of Invention
The invention overcomes the defects of the prior art and provides a tobacco germ solution mixing microscopic device and a control method thereof.
In order to achieve the purpose, the invention adopts the technical scheme that: a tobacco germ solution mixing microscopic device comprises: a mixing mechanism and a microscopic mechanism, wherein,
the mixing mechanism comprises a plurality of liquid storage tanks at the top, a mixer is arranged on the lower side of each liquid storage tank, a flow dividing assembly is arranged at the bottom of the mixer, a collecting part is connected to the bottom of the flow dividing assembly, the flow dividing assembly comprises a plurality of transfer mechanisms, one side of each transfer mechanism is connected with a first flow dividing channel through a first hinge part, the other side of each transfer mechanism is connected with a second flow dividing channel through a second hinge part, the transfer mechanisms can swing, and the transfer mechanisms are distributed in a circumferential array manner;
the mixing mechanism is connected with a microscopic mechanism in a matched mode, the microscopic mechanism comprises an observation table and a microscope, a solution cavity is arranged at the top of the observation table, a backflow box is arranged at the top of the observation table, one side of the backflow box is connected to the mixer, the backflow box is communicated with the solution cavity, pathogen solution in the mixer circulates through the solution cavity, and the microscope is used for observing the pathogen solution in the solution cavity in real time.
In a preferred embodiment of the invention, a plurality of liquid storage tanks are distributed in an array, the bottoms of the liquid storage tanks are converged into a same liquid inlet channel, the bottom of the liquid inlet channel is connected to a mixer, and the size of the upper part of the liquid inlet channel is larger than that of the lower part of the liquid inlet channel.
In a preferred embodiment of the present invention, a flow guide tube is connected to the bottom of the collecting member, one end of the flow guide tube is connected to the observation platform, and a valve is disposed between the flow guide tube and the collecting member.
In a preferred embodiment of the present invention, a vertical plate is disposed on the top of the reflow box, and an auxiliary mirror is disposed on one side of the vertical plate and is matched with the microscope.
In a preferred embodiment of the invention, a transverse plate is arranged on one side of the vertical plate, the transverse plate and the vertical plate are perpendicular to each other, the top of the transverse plate is connected with a display screen through a support member, a suspension column is arranged at the bottom of the transverse plate, a movable plate is movably connected to the bottom of the suspension column, a plurality of microscopes are arranged at the bottom of the movable plate, and the plurality of microscopes are distributed in a circumferential array manner.
In a preferred embodiment of the invention, a sliding plate is arranged on one side of the return box, a moving plate is connected to the sliding plate in a matching manner, the moving plate can vertically slide along the sliding plate, an observation hole is formed in the moving plate, a rotating disc is arranged at the bottom of the moving plate, a plurality of times of lenses are arranged on the rotating disc, and the times of lenses are matched with the observation hole.
In a preferred embodiment of the present invention, a flow inlet pipe and a flow return pipe are disposed at one side of the mixer, one end of the flow inlet pipe and one end of the flow return pipe are connected to a flow return box, and the flow inlet pipe and the flow return pipe form a circulation loop.
In a preferred embodiment of the invention, a rotating mechanism is arranged at the bottom of the observation platform, a base is connected to the bottom of the rotating mechanism, a plurality of rollers are arranged at intervals at the bottom of the base, and a locking mechanism is arranged on at least one roller.
In order to achieve the purpose, the invention adopts another technical scheme as follows: a control method of a mixed microscopic device is applied to a tobacco germ solution mixed microscopic device and comprises the following steps:
collecting germs on different tobacco plants, and storing a germ solution through a liquid storage tank;
germ solutions in different liquid storage tanks enter a mixer for premixing, and the germ solutions entering the mixer flow to a solution cavity through an inflow pipe and a return pipe;
adjusting the corresponding double-lens by a rotary disc, and adjusting the angle of the microscope by a movable plate to correspond to the position of the observation hole;
observing the germ solution in the solution cavity in real time through a microscope, wherein the germ solution is in a flowing state in the observation process;
the germ solution in the return pipe flows back to the mixer again, then the germ solution is shunted through the first shunting channel, the shunted germ solution enters the transfer mechanism to be mixed, the mixed germ solution is subjected to the second shunting channel, and the germ solution shunted through the second shunting channel enters the collecting piece.
In a preferred embodiment of the invention, the display image of the microscope is transmitted in real time through the display screen, and the distance between the observation hole and the solution cavity is adjusted by sliding the moving plate in the observation process.
The invention solves the defects in the background technology, and has the following beneficial effects:
(1) through the matching connection of the mixing mechanism and the microscopic mechanism, and the formation of a circulation loop through the solution cavity, the inflow pipe and the return pipe, the tobacco germ solution in the solution cavity can be observed in real time through a microscope in the mixing process, the targeted control of bacterial wilt is formed according to the analysis result, and the analysis value of the tobacco germ solution is improved.
(2) The distance between the observation hole and the solution cavity is adjusted by adjusting the distance between the moving plate and the solution cavity, and a proper microscope is selected by matching with the rotary disc, so that the observation precision of the microscope is improved.
(3) Germ solution is at the mixing process, through setting up transfer mechanism to improve heat-conduction effect through the heat-conducting piece on the transfer mechanism, and transfer mechanism realizes the swing through the articulated elements, rocks the germ solution in the transfer mechanism, and the mixing effect is better.
(4) Solution after the blender mixes gets into transfer mechanism through first reposition of redundant personnel passageway and carries out the secondary and mixes, and solution after the secondary mixes collects the piece through the second reposition of redundant personnel passageway, realizes mixing once more promptly in collecting the piece, through mixing many times, and keeps solution low flow through first reposition of redundant personnel passageway and second reposition of redundant personnel passageway and mix, and this kind of mode can maximize improvement mixing effect, is favorable to the high-efficient prevention and cure of bacterial wilt.
Drawings
The invention is further illustrated with reference to the following figures and examples.
FIG. 1 is a schematic perspective view of a tobacco pathogen solution mixing microscopic device according to the present invention;
FIG. 2 is a schematic view showing a partial structure of a microscopic assembly in a preferred embodiment of the present invention;
FIG. 3 is a schematic perspective view of a portion of a viewing station in accordance with a preferred embodiment of the present invention;
FIG. 4 is a partial schematic view of the telescope and the spinning disk according to the preferred embodiment of the present invention;
in the figure: 1. a liquid storage tank; 2. a liquid inlet channel; 3. a mixer; 4. a first diversion channel; 5. a first hinge member; 7. A transfer mechanism; 8. a second hinge member; 9. a second diversion channel; 10. a collecting member; 11. a flow guide pipe; 12. a return tank; 1201. a first knob; 1202. a slide plate; 13. an observation stage; 1301. a second knob; 14. a roller; 15. a locking mechanism; 16. a rotating mechanism; 17. a solution chamber; 18. moving the plate; 1801. an observation hole; 1802. rotating the disc; 1803. a double mirror; 19. a microscope; 20. a transverse plate; 21. a display screen; 2101. a control key; 22. an auxiliary mirror; 23. a vertical plate; 24. an inlet pipe; 25. a return pipe; 26. hinging a shaft; 27. a suspension post; 28. a movable plate.
Detailed Description
In order that the above objects, features and advantages of the present invention can be more clearly understood, a more particular description of the invention will be rendered by reference to the appended drawings. It should be noted that the embodiments and features of the embodiments of the present application may be combined with each other without conflict. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
In the following description, numerous specific details are set forth in order to provide a thorough understanding of the present invention, but the present invention may be practiced in other ways than those specifically described herein, and therefore the scope of the present invention is not limited by the specific embodiments disclosed below.
In the description of the present invention, it is to be understood that the terms "center", "longitudinal", "lateral", "up", "down", "front", "back", "left", "right", "vertical", "horizontal", "top", "bottom", "inner", "outer", etc. indicate orientations or positional relationships based on those shown in the drawings, and are used merely for convenience in describing the present invention and for simplicity in description, and do not indicate or imply that the device or element being referred to must have a particular orientation, be constructed and operated in a particular orientation, and therefore, should not be taken as limiting the scope of the present invention. Furthermore, the terms "first," "second," and the like are used for descriptive purposes only and are not to be construed as indicating or implying relative importance or implicitly indicating the number of technical features indicated. Thus, a feature defined as "first," "second," etc. may explicitly or implicitly include one or more of that feature. In the description of the invention, the meaning of "a plurality" is two or more unless otherwise specified.
In the description of the present invention, it should be noted that, unless otherwise explicitly specified or limited, the terms "mounted," "connected," and "connected" are to be construed broadly, e.g., as meaning either a fixed connection, a removable connection, or an integral connection; can be mechanically or electrically connected; they may be connected directly or indirectly through intervening media, or they may be interconnected between two elements. The specific meaning of the above terms in the present invention can be understood by those of ordinary skill in the art through specific situations.
FIG. 1 is a schematic perspective view of a tobacco pathogen solution mixing microscopic device according to the present invention.
As shown in fig. 1, the first aspect of the present invention provides a tobacco germ solution mixing microscopic device, comprising: a mixing mechanism and a microscopic mechanism, wherein,
the mixing mechanism comprises a plurality of liquid storage tanks 1 at the top, a mixer 3 is arranged on the lower side of each liquid storage tank 1, a flow dividing assembly is arranged at the bottom of each mixer 3, a collecting part 10 is connected to the bottom of each flow dividing assembly, each flow dividing assembly comprises a plurality of transfer mechanisms 7, one side of each transfer mechanism 7 is connected with a first flow dividing channel 4 through a first hinge part 5, the other side of each transfer mechanism 7 is connected with a second flow dividing channel 9 through a second hinge part 8, each transfer mechanism 7 can swing, and the plurality of transfer mechanisms 7 are distributed in a circumferential array manner;
the mixing mechanism cooperation is connected with the micro-mechanism, and the micro-mechanism includes observation platform 13 and microscope 19, and observation platform 13 top is provided with solution cavity 17, and observation platform 13 top is provided with backward flow case 12, and backward flow case 12 one side is connected to blender 3, and backward flow case 12 intercommunication solution cavity, germ solution in the blender 3 circulate through the circulation of solution cavity, and microscope 19 is used for observing the germ solution in the solution cavity in real time.
It should be noted that germ solution is at the hybrid process, through setting up relay mechanism 7, and improve heat conduction effect through the heat-conducting piece on the relay mechanism 7, and relay mechanism 7 realizes the swing through the articulated elements, rock the germ solution in the relay mechanism 7, the mixing effect is better, the solution after the blender 3 mixes carries out the secondary through first diversion channel 4 entering relay mechanism 7 and mixes, the solution after the secondary mixes carries out collecting part 10 through second diversion channel 9, realize the remixing in collecting part 10 promptly, through mixing many times, and keep solution low flow through first diversion channel 4 and second diversion channel 9 and mix, this kind of mode can the maximize improves the mixing effect, be favorable to the high-efficient prevention and cure of bacterial wilt.
According to the embodiment of the invention, a plurality of liquid storage tanks 1 are distributed in an array, the bottoms of the liquid storage tanks 1 are converged to the same liquid inlet channel 2, the bottom of the liquid inlet channel 2 is connected to a mixer 3, and the size of the upper part of the liquid inlet channel 2 is larger than that of the lower part of the liquid inlet channel 2.
According to the embodiment of the invention, the bottom of the collecting part 10 is connected with a flow guide tube 11, one end of the flow guide tube 11 is connected to an observation platform 13, and a valve is arranged between the flow guide tube 11 and the collecting part 10.
It should be noted that the valve is a fluid valve, including a throttle valve, a check valve, and an overflow valve, and is controlled in multiple ways by one or a combination of two or three of them, and the fluid flow is controlled by changing the section or length. The throttle valve and the one-way valve are connected in parallel to form the one-way throttle valve, the throttle valve and the one-way throttle valve are simple flow control valves, and the throttle valve is matched with the overflow valve to form a throttle speed regulating system.
According to the embodiment of the invention, the top of the return box 12 is provided with a vertical plate 23, one side of the vertical plate 23 is provided with an auxiliary mirror 22, and the auxiliary mirror 22 is matched with the microscope 19.
It should be noted that the angle between the auxiliary mirror 22 and the vertical plate is 45 degrees, the axis of the auxiliary mirror 22 intersects with the center of the observation hole, the first knob 1201 is disposed on one side of the vertical plate 23, the first knob 1201 is used to control the moving displacement of the moving plate 18, the distance between the observation hole 1801 on the moving plate 18 and the solution cavity 17 is adjusted by rotating the first knob 1201, the second knob 1301 is disposed on one side of the observation platform 13, and the movable plate 28 is controlled by the second knob 1301 to perform fine adjustment.
As shown in FIG. 2, the invention discloses a partial structure schematic diagram of a microscopic component.
According to the embodiment of the invention, a transverse plate 20 is arranged on one side of the vertical plate 23, the transverse plate 20 is perpendicular to the vertical plate 23, the top of the transverse plate 20 is connected with a display screen 21 through a support member, a suspension column 27 is arranged at the bottom of the transverse plate 20, a movable plate 28 is movably connected to the bottom of the suspension column 27, a plurality of microscopes 19 are arranged at the bottom of the movable plate 28, and the plurality of microscopes 19 are distributed in a circumferential array manner.
It should be noted that, a hinge shaft 26 is arranged on one side of the display screen 21, a light source is arranged on the hinge shaft 26, the brightness of the observation environment of the microscope device can be adjusted through the light source, so that tobacco germ analysis can be more accurately performed, the bottom of the movable plate 28 is of a convex structure, the microscopes 19 are arranged on the convex structure, the number of the microscopes 19 is 3, the angle between 3 microscopes 19 is 120 degrees, the movable plate 28 is movably connected with the suspension column 27 through a ball, the movable plate 28 can rotate at a wide angle through the ball, a control key 2101 is further arranged on the display screen 21, and the setting of the state parameters of the display screen 21 is performed through the control key 2101.
As shown in fig. 4, the present invention discloses a schematic view of a partial structure of a telescope and a rotating disk.
According to the embodiment of the invention, a sliding plate is arranged on one side of the return box 12, a moving plate 18 is connected to the sliding plate 1202 in a matching manner, the moving plate 18 can vertically slide along the sliding plate 1202, an observation hole 1801 is formed in the moving plate 18, a rotating disc 1802 is arranged at the bottom of the moving plate 18, a plurality of double mirrors 1803 are arranged on the rotating disc 1802, and the double mirrors 1803 are matched with the observation hole 1801.
It should be noted that the rotating disk 1802 has a circular structure, 12 mirrors 1803 are provided on the rotating disk 1802, the distances between adjacent mirrors 1803 are the same, and the mirrors 1803 are replaced by rotating the rotating disk 1802 thirty degrees each time the mirrors 1803 are adjusted.
According to the embodiment of the invention, one side of the mixer 3 is provided with the inlet pipe 24 and the return pipe 25, one end of the inlet pipe 24 and one end of the return pipe 25 are connected to the return tank 12, and the inlet pipe 24 and the return pipe 25 form a circulation loop.
According to the embodiment of the invention, a rotating mechanism 16 is arranged at the bottom of the observation platform 13, a base is connected to the bottom of the rotating mechanism 16, a plurality of rollers 14 are arranged at intervals at the bottom of the base, and a locking mechanism 15 is arranged on at least one roller 14.
In order to achieve the purpose, the invention adopts another technical scheme as follows: a control method of a mixed microscopic device is applied to a tobacco germ solution mixed microscopic device and comprises the following steps:
collecting germs on different tobacco plants, and storing a germ solution through a liquid storage tank 1;
germ solutions in different liquid storage tanks 1 enter a mixer 3 for premixing, the germ solutions entering the mixer 3 flow to a solution cavity 17 through an inlet pipe 24 and a return pipe 25,
adjusting the corresponding microscope 1803 through the rotary disc 1802, and adjusting the angle of the microscope 19 through the movable plate 28 to correspond to the position of the observation hole 1801;
the germ solution in the solution cavity 17 is observed in real time through a microscope 19, and the germ solution is in a flowing state in the observation process;
the germ solution in the return pipe 25 returns to the mixer 3 again, then the germ solution is shunted through the first shunt passage 4, the shunted germ solution enters the transfer mechanism 7 to be mixed, the mixed germ solution enters the second shunt passage 9, and the germ solution shunted through the second shunt passage 9 enters the collecting element 10.
According to the embodiment of the invention, a plurality of liquid storage tanks 1 are distributed in an array, the bottoms of the liquid storage tanks 1 are collected to the same liquid inlet channel 2, the bottom of the liquid inlet channel 2 is connected to a mixer 3, the size of the upper part of the liquid inlet channel 2 is larger than that of the lower part of the liquid inlet channel 2, the bottom of a collecting part 10 is connected with a flow guide pipe 11, one end of the flow guide pipe 11 is connected to an observation platform 13, a valve is arranged between the flow guide pipe 11 and the collecting part 10, the top of a return tank 12 is provided with a vertical plate 23, one side of the vertical plate 23 is provided with an auxiliary mirror 22, and the auxiliary mirror 22 is matched with a microscope 19.
It should be noted that the angle between the auxiliary mirror 22 and the vertical plate is 45 degrees, the axis of the auxiliary mirror 22 intersects with the center of the observation hole, the first knob 1201 is disposed on one side of the vertical plate 23, the first knob 1201 is used to control the moving displacement of the moving plate 18, the distance between the observation hole 1801 on the moving plate 18 and the solution cavity 17 is adjusted by rotating the first knob 1201, the second knob 1301 is disposed on one side of the observation platform 13, and the movable plate 28 is controlled by the second knob 1301 to perform fine adjustment.
1 array distribution of a plurality of liquid reserve tank, 1 bottom of a plurality of liquid reserve tank collects to same inlet channel 2, 2 bottoms of inlet channel are connected to blender 3, the size on 2 upper portions of inlet channel is greater than the size of 2 lower parts of inlet channel, collect 10 bottoms and be connected with honeycomb duct 11, honeycomb duct 11 one end is connected to observation platform 13, be provided with the valve between honeycomb duct 11 and the collection 10, also be provided with the valve on inflow pipe 24 and the back flow 25, germ solution through the different mixing stage of valve control gets into solution cavity 17 and observes the analysis, thereby form the sample contrast.
According to the embodiment of the invention, one side of each intermediate mechanism is connected with a first diversion channel through a first hinge element, the other side of each intermediate mechanism is connected with a second diversion channel through a second hinge element, the intermediate mechanisms can swing, a plurality of intermediate mechanisms are distributed in a circumferential array mode, one side of any intermediate mechanism is provided with a heat conducting piece, the bottom of a collecting piece is provided with a balance piece, and the bottom of the balance piece is provided with a connecting piece.
It should be noted that, the balance piece is a gyro structure, the mixing mechanism can be kept balanced in the rotating process through the gyro structure, the centrifugal force of the object rotating at high speed is large, after the center of gravity deviates from the central line, the centrifugal force can pull back the object, the safety is improved, the collecting piece is a detachable structure, and the rigid body of the gyroscope rotating at high speed around a fulcrum is called as a gyro. The gyroscope is a rigid body with uniformly distributed mass and axisymmetric shape, the geometric symmetry axis is its rotation axis, under a certain initial condition and a certain external moment, the gyroscope will rotate around another fixed rotation axis continuously while rotating continuously, that is, the precession of the gyroscope is also called as the gyroscopic effect, when the rotor rotates at high speed, if an external moment acts on the outer ring axis, the gyroscope will rotate around the inner ring axis, and if an external moment acts on the inner ring axis, the gyroscope will rotate around the outer ring axis. The direction of the rotational angular velocity is perpendicular to the direction of the external moment.
As shown in FIG. 3, the invention discloses a partial three-dimensional structure diagram of an observation platform.
According to the embodiment of the invention, the bottom of the movable plate 28 is a convex structure, the microscopes 19 are located on the convex structure, the number of the microscopes 19 is 3, the angle between the 3 microscopes 19 is 120 degrees, the movable plate 28 is movably connected with the suspension column 27 through balls, the movable plate 28 can rotate in a wide angle through the balls, the display picture of the microscope 19 is transmitted in real time through the display screen 21, and the distance between the observation hole 1801 and the solution cavity 17 is adjusted through sliding the movable plate 18 in the observation process.
It should be noted that the microscope in the present application combines a conventional microscope with an image pickup system, a display or a computer to achieve the purpose of magnifying and observing the object to be measured, and simultaneously transmits the observed picture or image to the display screen. The microscope may be a camera type microscope, and the image obtained under the microscope is projected onto the photo-sensitive picture by the principle of pinhole imaging, so as to obtain the picture, or the camera is directly docked with the microscope to take the picture. The microscope can also be a CCD camera, a real-time image can be transferred to a television or a monitor through the microscope for direct observation and shooting through the camera, the position of the top of the solution cavity corresponding to the microscope is of a transparent structure and is convenient for observation, the microscope in the application can also be a biological microscope for observing and researching biological slices, biological cells, bacteria, living tissue culture, fluid sediments and the like, other transparent or semitransparent objects, powder, fine particles and other objects can be observed at the same time, the biological cells in the ralstonia solanacearum solution can be observed clearly, the microscope device also comprises a control module and a transmission module, the transmission module transmits the picture monitored by the microscope 19 to a display screen 21 in real time, the analysis module is called through the control module to analyze the components of the tobacco germ solution, and the obtained data are recorded, the transmission module is electrically connected with the control module.
According to the embodiment of the invention, a sliding plate is arranged on one side of the return box 12, a moving plate 18 is connected to the sliding plate 1202 in a matching manner, the moving plate 18 can slide vertically along the sliding plate 1202, an observation hole 1801 is formed in the moving plate 18, a rotating disc 1802 is arranged at the bottom of the moving plate 18, a plurality of double mirrors 1803 are arranged on the rotating disc 1802, the double mirrors 1803 are matched with the observation hole 1801, a transverse plate 20 is arranged on one side of a vertical plate 23, the transverse plate 20 is perpendicular to the vertical plate 23, a display screen 21 is connected to the top of the transverse plate 20 through a supporting member, a suspension column 27 is arranged at the bottom of the transverse plate 20, a moving plate 28 is movably connected to the bottom of the suspension column 27, a plurality of microscopes 19 are arranged at the bottom of the moving plate 28, and the plurality of microscopes 19 are distributed in a circumferential array manner.
It should be noted that one side of the display screen 21 is provided with a hinge shaft 26, the hinge shaft 26 is provided with a light source, brightness of an observation environment of the microscope device can be adjusted through the light source, so that tobacco germ analysis can be more accurately performed, the bottom of the movable plate 28 is of a convex structure, the microscopes 19 are located on the convex structure, the number of the microscopes 19 is 3, angles among the 3 microscopes 19 are 120 degrees, the movable plate 28 is movably connected with the suspension columns 27 through balls, the movable plate 28 can rotate at a wide angle through the balls, the display screen 21 is further provided with control keys 2101, status parameters of the display screen 21 are set through the control keys 2101, the rotating disc 1802 is of a circular structure, 12 times of the rotating disc 1802 are provided, intervals among adjacent times of the rotating disc 1803 are the same, and when the times of the rotating disc 1802 are adjusted, the times of the rotating disc 1803 are changed thirty degrees.
In conclusion, the mixing mechanism is connected with the microscopic mechanism in a matching manner, and a circulation loop is formed by the solution cavity 17, the inflow pipe 24 and the return pipe 25, so that the tobacco germ solution in the solution cavity 17 can be observed in real time through the microscope 19 in the mixing process, the treatment of the bacterial wilt pertinence is formed according to the analysis result, the analysis value of the tobacco germ solution is improved, the distance between the observation hole 1801 and the solution cavity 17 is adjusted by adjusting the distance between the moving plate 18 and the solution cavity 17, and in addition, the proper times of the microscope 1803 is selected by matching with the rotary disc 1802, so that the observation precision of the microscope 19 is improved.
In the several embodiments provided in the present application, it should be understood that the disclosed apparatus and method may be implemented in other ways. The above-described device embodiments are merely illustrative, for example, the division of a unit is only one logical function division, and there may be other division ways in actual implementation, such as: multiple units or components may be combined, or may be integrated into another system, or some features may be omitted, or not implemented. In addition, the coupling, direct coupling or communication connection between the components shown or discussed may be through some interfaces, and the indirect coupling or communication connection between the devices or units may be electrical, mechanical or other forms.
The units described as separate parts may or may not be physically separate, and parts displayed as units may or may not be physical units; can be located in one place or distributed on a plurality of network units; some or all of the units can be selected according to actual needs to achieve the purpose of the solution of the embodiment.
In addition, all the functional units in the embodiments of the present invention may be integrated into one processing unit, or each unit may be separately regarded as one unit, or two or more units may be integrated into one unit; the integrated unit can be realized in a form of hardware, or in a form of hardware plus a software functional unit.
Those of ordinary skill in the art will understand that: all or part of the steps for realizing the method embodiments can be completed by hardware related to program instructions, the program can be stored in a computer readable storage medium, and the program executes the steps comprising the method embodiments when executed; and the aforementioned storage medium includes: a mobile storage device, a Read-Only Memory (ROM), a Random Access Memory (RAM), a magnetic disk or an optical disk, and other various media capable of storing program codes.
Alternatively, the integrated unit of the present invention may be stored in a computer-readable storage medium if it is implemented in the form of a software functional module and sold or used as a separate product. Based on such understanding, the technical solutions of the embodiments of the present invention may be essentially implemented or a part contributing to the prior art may be embodied in the form of a software product, which is stored in a storage medium and includes several instructions for enabling a computer device (which may be a personal computer, a server, or a network device) to execute all or part of the methods of the embodiments of the present invention. And the aforementioned storage medium includes: a removable storage device, a ROM, a RAM, a magnetic or optical disk, or various other media that can store program code.
The above description is only for the specific embodiments of the present invention, but the scope of the present invention is not limited thereto, and any person skilled in the art can easily conceive of the changes or substitutions within the technical scope of the present invention, and the changes or substitutions should be covered within the scope of the present invention. Therefore, the protection scope of the present invention shall be subject to the protection scope of the claims.
Claims (6)
1. A tobacco germ solution mixing microscopic device comprises: the mixing mechanism is characterized by comprising a plurality of liquid storage tanks at the top, a mixer is arranged on the lower side of each liquid storage tank, a flow dividing assembly is arranged at the bottom of the mixer, a collecting piece is connected to the bottom of the flow dividing assembly, the flow dividing assembly comprises a plurality of transfer mechanisms, one side of each transfer mechanism is connected with a first flow dividing channel through a first hinge piece, the other side of each transfer mechanism is connected with a second flow dividing channel through a second hinge piece, the transfer mechanisms can swing, and the transfer mechanisms are distributed in a circumferential array manner;
the mixing mechanism is connected with a microscope mechanism in a matching manner, the microscope mechanism comprises an observation platform and a microscope, a solution cavity is arranged at the top of the observation platform, a backflow box is arranged at the top of the observation platform, one side of the backflow box is connected to the mixer, the backflow box is communicated with the solution cavity, a germ solution in the mixer circulates through the solution cavity, and the microscope is used for observing the germ solution in the solution cavity in real time;
a vertical plate is arranged at the top of the reflux box, an auxiliary mirror is arranged on one side of the vertical plate, and the auxiliary mirror is matched with the microscope;
a transverse plate is arranged on one side of the vertical plate and is perpendicular to the vertical plate, the top of the transverse plate is connected with a display screen through a support piece, a suspension column is arranged at the bottom of the transverse plate, a movable plate is movably connected to the bottom of the suspension column, a plurality of microscopes are arranged at the bottom of the movable plate, and the plurality of microscopes are distributed in a circumferential array manner;
a plurality of liquid reserve tank array distributes, a plurality of liquid reserve tank bottom collects to same inlet channel, the inlet channel bottom is connected to the blender, the size on inlet channel upper portion is greater than the size of inlet channel lower part, it is connected with the honeycomb duct to collect a bottom, honeycomb duct one end is connected to the observation platform, be provided with the valve between honeycomb duct and the collection piece, also be provided with the valve on inflow pipe and the back flow, get into the solution cavity through the different mixing stage of valve control and observe the analysis, thereby form the sample contrast.
2. The tobacco germ solution mixing microscope device as claimed in claim 1, wherein a slide plate is disposed on one side of the return box, a moving plate is cooperatively connected to the slide plate, the moving plate can vertically slide along the slide plate, a viewing hole is disposed on the moving plate, a rotating disc is disposed at the bottom of the moving plate, a plurality of times of mirrors are disposed on the rotating disc, and the times of mirrors are matched with the viewing hole.
3. A tobacco pathogen solution mixing microscopic device according to any one of claims 1-2, characterized in that a flow inlet pipe and a return pipe are arranged on one side of the mixer, one end of the flow inlet pipe and one end of the return pipe are connected to a return tank, and the flow inlet pipe and the return pipe form a circulation loop.
4. The tobacco germ solution mixing microscope device as claimed in claim 1, wherein a rotating mechanism is arranged at the bottom of the observation platform, a base is connected to the bottom of the rotating mechanism, a plurality of rollers are arranged at intervals at the bottom of the base, and a locking mechanism is arranged on at least one roller.
5. A control method of a mixing microscope device, which is applied to the tobacco germ solution mixing microscope device of claim 3, and is characterized by comprising the following steps: collecting germs on different tobacco plants, and storing a germ solution through a liquid storage tank;
germ solutions in different liquid storage tanks enter a mixer for premixing, the germ solutions entering the mixer flow to a solution cavity through an inflow pipe and a return pipe, a corresponding microscope is adjusted through a rotary disc, and the angle of the microscope is adjusted through a movable plate to correspond to the position of an observation hole;
observing the germ solution in the solution cavity in real time through a microscope, wherein the germ solution is in a flowing state in the observation process;
the germ solution in the return pipe flows back to the mixer again, then the germ solution is shunted through the first shunting channel, the shunted germ solution enters the transfer mechanism to be mixed, the mixed germ solution is subjected to the second shunting channel, and the germ solution shunted through the second shunting channel enters the collecting piece.
6. The control method of claim 5, wherein the microscope display is transmitted in real time through the display screen, and the distance between the observation hole and the solution chamber is adjusted by sliding the moving plate during the observation process.
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| CN202110766874.8A CN113252675B (en) | 2021-07-07 | 2021-07-07 | Tobacco germ solution mixing microscopic device and control method thereof |
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| AU2002253773A1 (en) * | 2002-04-11 | 2003-11-17 | Gintic Institute Of Manufacturing Technology | Systems and methods for deformation measurement |
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| CN202077534U (en) * | 2010-12-29 | 2011-12-21 | 上海冠生园食品有限公司 | Solid particle and syrup even mixing device |
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