A kind of emamectin benzoate purity detection device and method
By designing a built-in detection auxiliary mechanism in the liquid chromatograph, and using the drive assembly and stirring assembly to achieve uniform heating and mixing of samples, the problem that existing liquid chromatographs cannot effectively control the initial temperature of the sample and mobile phase is solved, and the accuracy and reliability of the detection are improved.
Patent Information
- Application Number
- CN202510066429.9
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Filing Date
- 2025-01-16
- Publication Date
- 2025-04-08
- Estimated Expiration
- 2045-01-16
AI Technical Summary
During use, existing liquid chromatographs cannot effectively control the initial temperature of the samples entering externally and mobile phases, resulting in measurement errors and bubble generation, affecting the accuracy and reliability of the detection.
A A-dimensional salt purity detection device is designed, using a built-in detection auxiliary mechanism, including a drive assembly, a transmission assembly, agitating assembly and elastic assembly. The eccentric disc is driven by a motor to rotate, driving the shell to vibrate and stir, ensuring that the sample is heated and mixed in the spiral path evenly.
It effectively reduces bubble generation, stabilizes the detection baseline, improves the accuracy and reliability of detection, simplifies operations, and reduces costs.
Smart Images

Figure CN119470734B_ABST
Abstract
Description
Technical Field
[0001] The present invention relates to the technical field of purity detection, and in particular to a device and method for detecting the purity of emamectin benzoate. Background Art
[0002] In the process of purity detection of emamectin benzoate, it is often necessary to use a liquid chromatograph, which is an instrument that uses the difference in the distribution ratio of the mixture between liquid and solid or between two immiscible liquids to separate the mixture first and then analyze and identify it. It is widely used in biochemistry, food analysis, medical research, environmental analysis, inorganic analysis and other occasions, and has good use effect.
[0003] At present, the mainstream liquid chromatography technology framework is mainly composed of core components such as high-pressure infusion pumps, precision injection systems, temperature control systems, high-efficiency chromatographic columns, high-sensitivity detectors, and precise signal recording systems. Both temperature and uniformity can affect the results of the analysis, thereby affecting the separation performance of the column and the viscosity of the mobile phase. Therefore, ensuring a constant column temperature is very important for the accuracy and repeatability of the results. In addition to the column temperature control system, the initial temperature of the sample and mobile phase entering from the outside will also affect the control stability of the column temperature. However, when the existing liquid chromatograph is in use, the sample and mobile phase entering from the outside are not heated, which leads to certain errors in the measurement process of the liquid chromatograph, reducing the accuracy of the liquid chromatograph measurement.
[0004] In addition to the core link of column temperature control, the initial temperature of the externally introduced sample and mobile phase also has an important impact on the stability of column temperature control. Unfortunately, in the routine operation of existing liquid chromatographs, the preheating of external samples and mobile phases is often neglected. This omission leads to the introduction of unnecessary errors in the measurement process, which in turn weakens the accuracy of the instrument measurement. What is more serious is that with the increase of temperature, the solubility of the gas in the solvent will decrease significantly, thereby precipitating and forming bubbles. At the same time, the reduction of pressure in the system will also become a cause of bubble generation. These bubbles will not only cause baseline fluctuations and increase in noise levels, but also seriously interfere with the clarity of the detection signal, making it difficult to accurately identify and quantitatively analyze the chromatographic peaks; moreover, they may also disrupt the normal operation of the pump, resulting in unstable flow rate fluctuations, which has a negative impact on the separation effect. Once the bubbles invade the interior of the chromatographic column, they will change the flow rate distribution of the mobile phase in the column, resulting in a decrease in column efficiency, which seriously affects the separation effect of the sample.
[0005] In view of the above problems, the present invention document proposes a device and method for detecting the purity of emamectin benzoate. Summary of the invention
[0006] The purpose of the present invention is to solve the shortcomings of the liquid chromatograph in the prior art that it is unable to uniformly control the initial temperature of the sample and mobile phase entering from the outside and that bubbles are easily generated during use, and to propose a device and method for detecting the purity of emamectin benzoate.
[0007] In order to achieve the above object, the present invention adopts the following technical solutions:
[0008] A device for detecting purity of emamectin benzoate, comprising a liquid chromatograph, wherein a cavity is provided in the middle and upper part of the liquid chromatograph, and a built-in detection auxiliary mechanism is installed inside the cavity;
[0009] The built-in detection auxiliary mechanism includes an external support component and a conveying component. A driving component is installed in the middle of the external support component. A transmission component is arranged below the driving component. The transmission component passes through the conveying component and is connected to the vibration component. The vibration component is located below the conveying component. Four stirring components are arranged inside the conveying component. One end of the four stirring components is connected to the transmission component for transmission. Four elastic components are arranged outside the conveying component, and the four elastic components are arranged in the external support component.
[0010] Preferably, the external support component includes a support frame, four first slide grooves are opened inside the support frame, support columns are installed at the four corners of the support frame, reinforcement rods are fixedly connected to the top of the support columns, and mounting plates are fixedly connected to the upper and lower ends of the support columns, and the mounting plates are fixedly connected in the cavity.
[0011] Preferably, the conveying assembly comprises a shell, the outer portion of the shell is provided with four second slide grooves, and the bottom of the shell is fixedly connected with a plurality of convex balls arranged in an annular manner;
[0012] A spiral path is provided inside the shell, and a plurality of heating plates are installed inside the spiral path, a gap is reserved between the heating plates and the inner wall of the spiral path, and every three heating plates are staggered;
[0013] Both sides of the shell are provided with connecting pipes, the connecting pipes are soft pipes, and one end of the two connecting pipes is connected with the liquid chromatograph.
[0014] Preferably, the stirring assembly includes a rotating shaft, which is arranged transversely across the spiral path and rotatably mounted on the side wall of the spiral path through multiple bearings. Multiple stirring blades are fixedly connected to the outside of the rotating shaft, and one end of the rotating shaft is fixedly connected to a second bevel gear.
[0015] Preferably, the drive assembly includes a fixed frame, which is fixedly connected to four reinforcement rods, a gear ring is fixedly connected to the bottom of the fixed frame, a motor is installed in the middle of the fixed frame, the output shaft of the motor is fixedly connected to a transmission shaft, and the bottom end of the transmission shaft is fixedly connected to an eccentric disk.
[0016] Preferably, the transmission assembly comprises a polygonal shaft, the polygonal shaft is rotatably mounted on the eccentric disk via a bearing, a gear is fixedly connected to the top end of the polygonal shaft, and the gear is meshed with a gear ring.
[0017] Preferably, the polygonal shaft sleeve is provided with an inner sleeve, the outer part of the inner sleeve is fixedly connected to an outer sleeve, the outer sleeve is rotatably mounted on the outer shell through two bearings, the outer sleeve is fixedly connected to a first bevel tooth, and the first bevel tooth is meshed with four second bevel teeth.
[0018] Preferably, the vibration assembly includes a chassis, a plurality of balls are fixedly connected to the top of the chassis, the arrangement of the balls is the same as that of the convex balls, and the balls are in contact with the convex balls, and a third spring is fixedly connected to the top of the chassis, and the third spring is fixedly connected to the bottom of the inner sleeve.
[0019] Preferably, the elastic component includes a first slider, the first slider slides in a first slide groove, one side of the first slider is fixedly connected to two telescopic rods and two first springs, one end of the two telescopic rods and the two first springs is fixedly connected to a connecting plate, one side of the connecting plate is fixedly connected to a second slider, the second slider slides in a second slide groove, and a second spring is fixedly connected between the bottom of the second slider and the bottom wall of the second slide groove.
[0020] A method for using an emamectin benzoate purity detection device comprises the following steps:
[0021] S1. When the purity of emamectin benzoate is detected, the transmission shaft is driven to rotate by a motor, so that the transmission shaft drives the eccentric disk to rotate, and the rotation of the eccentric disk drives the transmission assembly to rotate, so that the housing follows the movement. Due to the eccentric movement of the eccentric disk, the eccentric disk cooperates with the first spring to realize the vibration of the housing;
[0022] S2. When the gear follows the movement of the eccentric disk, the gear and the gear ring are driven, the gear drives the polygonal shaft to rotate, the polygonal shaft drives the chassis to rotate, the chassis drives the ball to move, so that the ball and the convex ball are squeezed, the shell moves, and the ball cooperates with the second spring and the third spring to realize the vibration of the shell. The above operation makes the shell vibrate in multiple directions;
[0023] S3. When the polygonal shaft rotates, the polygonal shaft drives the inner sleeve to rotate, the inner sleeve drives the outer sleeve to rotate, the outer sleeve drives the first bevel gear to rotate, the first bevel gear and the second bevel gear drive, the second bevel gear drives the rotating shaft to rotate, and the rotating shaft drives the stirring blade to rotate;
[0024] S4. Then, the emamectin benzoate sample is transported downward through the top of the liquid chromatograph, and enters the spiral path from the connecting tube. The outer shell is vibrated in all directions to eliminate bubbles in the emamectin benzoate sample, and the emamectin benzoate sample is spirally transported along the spiral path. At the same time, it is heated by a heating plate and stirred multiple times by a stirring blade. Then, the emamectin benzoate sample is entered into the bottom of the liquid chromatograph through the connecting tube for purity detection of the emamectin benzoate sample.
[0025] Compared with the prior art, the present invention provides a device and method for detecting the purity of emamectin benzoate, which has the following beneficial effects:
[0026] 1. The emamectin benzoate purity detection device and method drive the transmission shaft and the eccentric disk to rotate through a motor, so that the eccentric disk drives the transmission component to rotate, and the gear and the gear ring can drive the polygonal shaft and the inner sleeve to rotate, so that the outer sleeve drives the first bevel gear and the stirring component to drive, and the emamectin benzoate sample is initially stirred after entering the spiral path, and then flows in a serpentine manner through the staggered heating plates, thereby facilitating the heating effect of the emamectin benzoate sample, and then the emamectin benzoate sample continues to flow along the spiral path, and is repeatedly heated and stirred for multiple times, thereby improving the heating uniformity and uniform mixing. Heating can enhance the molecular activity, help the sample to dissolve more evenly in the mobile phase, and promote chromatographic separation. At the same time, mixing can more accurately determine the content of the compound in the sample, thereby helping to improve the accuracy and reliability of detection.
[0027] 2. The device and method for detecting the purity of emamectin benzoate drive a transmission shaft to rotate through a motor, and the transmission shaft drives the eccentric disk to realize eccentric motion, so that the eccentric disk drives the outer shell to move through the transmission assembly, and the eccentric disk can cooperate with the first spring to realize the vibration of the outer shell, and the gear follows the rotation of the eccentric disk and can also be transmitted with the gear ring, so that the polygonal shaft drives the chassis to rotate, and the chassis drives the ball bearings and the convex balls to generate an extrusion motion, so that the ball bearings and the convex balls can cooperate with the third spring and the second spring to realize the vibration of the outer shell again, so that the multi-directional vibration of the outer shell can effectively reduce bubbles, and the baseline can be stabilized by eliminating bubbles, so that the analysis result is more stable.
[0028] 3. The device and method for detecting the purity of emamectin benzoate, by rotating the driving component, the eccentric movement of the eccentric disk can cooperate with the elastic component to realize the vibration of the shell, and at the same time, the driving component drives the transmission component to rotate, and the transmission component and the stirring component transmit, so that the stirring component rotates, and at the same time, the transmission component drives the vibration component to rotate, so that the vibration component and the conveying component produce an extrusion movement, and cooperate with the elastic component to realize multi-directional vibration of the shell, and the multi-directional vibration and the stirring component can improve the uniformity of mixing and heating of the emamectin benzoate sample, and help degas and exhaust the mobile phase, so as to greatly reduce the influence of bubbles on chromatographic separation and improve the separation effect, and this method is simple to operate and low in cost. BRIEF DESCRIPTION OF THE DRAWINGS
[0029] Figure 1 A three-dimensional view of a device for detecting purity of emamectin benzoate proposed by the present invention;
[0030] Figure 2 A three-dimensional view of a built-in detection auxiliary mechanism of an emamectin benzoate purity detection device proposed by the present invention;
[0031] Figure 3 This is a bottom-up stereoscopic view of a built-in detection auxiliary mechanism of an emamectin benzoate purity detection device proposed by the present invention;
[0032] Figure 4 A sectional stereoscopic view of an external support assembly of an emamectin benzoate purity detection device proposed by the present invention;
[0033] Figure 5 A sectional stereoscopic view of a conveying component of an emamectin benzoate purity detection device proposed by the present invention;
[0034] Figure 6 A three-dimensional cross-sectional view of the shell of an emamectin benzoate purity detection device proposed by the present invention;
[0035] Figure 7 For the present invention Figure 6 A magnified view of point A;
[0036] Figure 8 A three-dimensional view of a support frame of an emamectin benzoate purity detection device proposed by the present invention;
[0037] Fig. 9 A sectional stereoscopic view of a driving component of an emamectin benzoate purity detection device proposed by the present invention;
[0038] Fig.10 This is a three-dimensional view of the shell of an emamectin benzoate purity detection device proposed by the present invention.
[0039] In the figure: 100, liquid chromatograph; 101, cavity; 200, built-in detection auxiliary mechanism; 201, external support assembly; 2011, support frame; 2012, support column; 2013, mounting plate; 2014, reinforcement rod; 2015, first slide groove; 202, drive assembly; 2021, fixed frame; 2022, motor; 2023, eccentric plate; 2024, gear ring; 2025, transmission shaft; 203, elastic assembly; 2031, connecting plate; 2032, second spring; 2033, second slider; 2034, first spring; 2035, telescopic Rod; 2036, first slider; 204, transmission assembly; 2041, gear; 2042, polygonal shaft; 2043, inner sleeve; 2044, outer sleeve; 2045, first bevel gear; 205, vibration assembly; 2051, chassis; 2052, ball; 2053, third spring; 206, stirring assembly; 2061, stirring blade; 2062, second bevel gear; 2063, rotating shaft; 207, conveying assembly; 2071, housing; 2072, connecting pipe; 2073, spiral path; 2074, heating plate; 2075, second slide groove; 2076, convex ball. DETAILED DESCRIPTION
[0040] The technical solutions in the embodiments of the present invention will be described clearly and completely below in conjunction with the drawings in the embodiments of the present invention. Obviously, the described embodiments are only part of the embodiments of the present invention, rather than all the embodiments.
[0041] In the description of the present invention, it is necessary to understand that the terms "upper", "lower", "front", "back", "left", "right", "top", "bottom", "inside", "outside", etc., indicating the orientation or position relationship are based on the orientation or position relationship shown in the drawings, and are only for the convenience of describing the present invention and simplifying the description, rather than indicating or implying that the device or element referred to must have a specific orientation, be constructed and operated in a specific orientation, and therefore cannot be understood as a limitation on the present invention.
[0042] Example 1: Reference Figure 1-Figure 9 , a purity detection device of emamectin benzoate, comprising a liquid chromatograph 100, wherein a cavity 101 is provided in the middle and upper part of the liquid chromatograph 100, and a built-in detection auxiliary mechanism 200 is installed inside the cavity 101;
[0043] The built-in detection auxiliary mechanism 200 includes an external support component 201 and a conveying component 207. The conveying component 207 includes a shell 2071. Four second slide grooves 2075 are provided on the outside of the shell 2071. A plurality of convex balls 2076 arranged in an annular manner are fixedly connected to the bottom of the shell 2071. A spiral path 2073 is provided inside the shell 2071. Since the spiral path 2073 is arranged in a spiral, the emamectin benzoate sample can flow in a spiral along the spiral path 2073, thereby increasing the stirring time and heating time of the emamectin benzoate sample. A plurality of heating plates 2074 are installed, and a gap is reserved between the heating plates 2074 and the inner wall of the spiral path 2073, and every three heating plates 2074 are staggered. The heating plates 2074 can heat the emamectin benzoate sample. Since the gap is reserved between the heating plates 2074 and the spiral path 2073, the emamectin benzoate sample can pass smoothly. At the same time, the gap can reduce the amount of emamectin benzoate sample passing through, so that the emamectin benzoate sample passes thinner, thereby facilitating the heating and mixing of the emamectin benzoate sample. In addition, connecting pipes 2072 are arranged on both sides of the housing 2071. The connecting pipes 2072 are connected to the housing 2071. 2 is a hose. By setting the connecting tube 2072 as a hose, the connecting tube 2072 can not only transport the emamectin benzoate sample, but also has retractability, so that the housing 2071 can vibrate smoothly. One end of the two connecting tubes 2072 is connected to the liquid chromatograph 100. The middle part of the external support assembly 201 is equipped with a driving assembly 202. The driving assembly 202 includes a fixing frame 2021. The fixing frame 2021 is fixedly connected to four reinforcing rods 2014. The fixing frame 2021 is connected to the reinforcing rods 2014 so that the fixing frame 202 1 can play a role in fixing the motor 2022, so as to maintain the stability of the motor 2022. A gear ring 2024 is fixedly connected to the bottom of the fixing frame 2021. The motor 2022 is installed in the middle of the fixing frame 2021. The output shaft of the motor 2022 is fixedly connected to the transmission shaft 2025. The transmission shaft 2025 is driven to rotate by the motor 2022, and the transmission shaft 2025 drives the eccentric disk 2023 to rotate, so that the eccentric centrifugal motion of the eccentric disk 2023 can realize the vibration operation of the housing 2071. The bottom end of the transmission shaft 2025 is fixedly connected to the eccentric disk 2023.
[0044] A transmission assembly 204 is arranged below the driving assembly 202. The transmission assembly 204 includes a polygonal shaft 2042. The polygonal shaft 2042 is rotatably mounted on the eccentric disk 2023 through a bearing. The polygonal shaft 2042 can maintain stable rotation through the bearing, so that the gear 2041 maintains stable rotation. The top of the polygonal shaft 2042 is fixedly connected with a gear 2041. The gear 2041 is meshed with the gear ring 2024. The gear 2041 and the gear ring 2024 are transmitted, so that power transmission can be achieved, so that the gear 2041 can drive the polygonal shaft 2042 to rotate. An inner sleeve 2043 is arranged on the outer sleeve of the polygonal shaft 2042. By setting the polygonal shaft 2042 to a polygonal structure and matching the inner opening shape of the inner sleeve 2043 with the polygonal shaft 2042, the polygonal shaft 2042 can be rotated stably. The rotation of the side shaft 2042 can drive the inner sleeve 2043 to rotate, and the inner sleeve 2043 can also move smoothly up and down along the polygonal shaft 2042. The outer sleeve 2044 is fixedly connected to the outside of the inner sleeve 2043. The outer sleeve 2044 is rotatably installed on the outer shell 2071 through two bearings. The outer sleeve 2044 can rotate smoothly through the bearings, so that the outer sleeve 2044 can drive the first bevel gear 2045 and the second bevel gear 2062 to stably transmit. The first bevel gear 2045 is fixedly connected to the outer sleeve 2044, and the first bevel gear 2045 is meshed with four second bevel gears 2062. The transmission is transmitted through the first bevel gear 2045 and the second bevel gear 2062, so that power transmission can be realized, so that the second bevel gear 2062 drives the rotating shaft 2063 to rotate, and the transmission component 204 passes through the conveying assembly 207 and is connected to the vibration assembly 205. The vibration assembly 205 is located below the conveying assembly 207. Four stirring assemblies 206 are arranged inside the conveying assembly 207. The stirring assembly 206 includes a rotating shaft 2063. The rotating shaft 2063 is arranged across the spiral path 2073. The rotating shaft 2063 is rotatably installed on the side wall of the spiral path 2073 through multiple bearings. The rotating shaft 2063 can rotate smoothly through the bearings, so that the rotating shaft 2063 drives the stirring blade 2061 to rotate smoothly, and then the stirring blade 2061 can stir the emamectin benzoate sample. Multiple stirring blades 2061 are fixedly connected to the outside of the rotating shaft 2063, and one end of the rotating shaft 2063 is fixedly connected to the second bevel gear 2062. The four stirring assemblies 206 One end is connected to the transmission component 204 for transmission. Four elastic components 203 are arranged outside the conveying component 207. The four elastic components 203 are arranged in the external support component 201. The external support component 201 includes a support frame 2011. Four first slide grooves 2015 are opened inside the support frame 2011. Support columns 2012 are installed at the four corners of the support frame 2011. The elastic components 203 can be limited and supported by the support frame 2011 to maintain the stability of the elastic components 203. The support frame 2011 is connected to the mounting plate 2013 through the support column 2012 to maintain the overall stability. A reinforcing rod 2014 is fixedly connected to the top of the support column 2012. The upper and lower ends of the support column 2012 are fixedly connected to the mounting plate 2013.The mounting plate 2013 is fixedly connected in the cavity 101.
[0045] In this embodiment, the motor 2022 drives the transmission shaft 2025 and the eccentric disk 2023 to rotate, so that the eccentric disk 2023 drives the transmission assembly 204 to rotate, and the gear 2041 and the gear ring 2024 drive the polygonal shaft 2042 and the inner sleeve 2043 to rotate, so that the outer sleeve 2044 drives the first bevel gear 2045 and the second bevel gear 2062 to drive, the second bevel gear 2062 drives the rotating shaft 2063 to rotate, and the rotating shaft 2063 drives the stirring blade 2061 to rotate. When the emamectin benzoate sample enters the spiral channel 2073 and enters The sample is first stirred for the first time, and then flows in a serpentine manner through the staggered heating plates 2074, thereby facilitating the heating effect of the emamectin benzoate sample. The emamectin benzoate sample is then allowed to continue to flow along the spiral path 2073, and repeated heating and stirring are performed for multiple times, thereby improving the heating uniformity and uniform mixing. Heating can enhance the activity of molecules, help the sample to dissolve more evenly in the mobile phase, promote chromatographic separation, and more accurately determine the content of the compound in the sample, thereby helping to improve the accuracy and reliability of the detection.
[0046] Example 2: Reference Figure 4 and Figure 9-10 A device for detecting purity of emamectin benzoate includes a vibration assembly 205. The vibration assembly 205 includes a chassis 2051. A plurality of balls 2052 are fixedly connected to the upper portion of the chassis 2051. The arrangement of the balls 2052 is the same as that of the convex balls 2076. The balls 2052 are in contact with the convex balls 2076. Since the balls 2052 have good rolling properties, when the balls 2052 are squeezed with the convex balls 2076, the friction resistance between the balls 2052 and the convex balls 2076 can be reduced, thereby improving the operation flow. The third spring 2053 is fixedly connected to the upper part of the chassis 2051. By connecting the third spring 2053 to the inner sleeve 2043, the inner sleeve 2043 moves with the outer shell 2071 to drive the third spring 2053 to deform. When the ball 2052 is separated from the convex ball 2076, the third spring 2053 can drive the outer shell 2071 to reset through the inner sleeve 2043, so as to perform reciprocating extrusion, so as to realize the vibration of the outer shell 2071. The third spring 2053 is fixedly connected to the lower part of the inner sleeve 2043.
[0047] The driving assembly 202 includes a fixed frame 2021, the fixed frame 2021 is fixedly connected to the four reinforcement rods 2014, a gear ring 2024 is fixedly connected to the bottom of the fixed frame 2021, a motor 2022 is installed in the middle of the fixed frame 2021, the output shaft of the motor 2022 is fixedly connected to the transmission shaft 2025, and the bottom end of the transmission shaft 2025 is fixedly connected to the eccentric disk 2023;
[0048] The elastic component 203 includes a first slider 2036, and the first slider 2036 slides in the first slide groove 2015. The first slider 2036 slides in the first slide groove 2015, so that the housing 2071 can be smoothly shaken in multiple directions. One side of the first slider 2036 is fixedly connected to two telescopic rods 2035 and two first springs 2034. Through the elasticity of the telescopic rods 2035 and the first springs 2034, the first springs 2034 can cooperate with the eccentric disk 2023 to achieve the vibration of the housing 2071. One end of the two telescopic rods 2035 and the two first springs 2034 is fixedly connected to the connecting plate 20 31. A second slider 2033 is fixedly connected to one side of the connecting plate 2031. The second slider 2033 slides in the second slide groove 2075. Since the shell 2071 can slide on the second slider 2033 through the second slide groove 2075, the sliding of the shell 2071 can drive the second spring 2032 to deform, and the second spring 2032 can assist the shell 2071 to reset, so that the second spring 2032 can cooperate with the ball 2052 and the convex ball 2076 to smoothly realize the vibration operation of the shell 2071. The second spring 2032 is fixedly connected between the bottom of the second slider 2033 and the bottom wall of the second slide groove 2075.
[0049] In this embodiment: the transmission shaft 2025 is driven to rotate by the motor 2022, and the transmission shaft 2025 drives the eccentric disk 2023 to realize eccentric movement, so that the eccentric disk 2023 drives the shell 2071 to move through the transmission assembly 204, and at the same time, the eccentric disk 2023 can cooperate with the first spring 2034 to realize the vibration of the shell 2071, and at the same time, the gear 2041 follows the rotation of the eccentric disk 2023 and can also be transmitted with the ring gear 2024, so that the polygonal shaft 2042 drives the chassis 2051 to rotate, and the chassis 2051 drives the ball 2052 and the convex ball 2076 to generate an extrusion movement, so that the ball 2052 and the convex ball 2076 can cooperate with the third spring 2053 and the second spring 2032 to realize the vibration of the shell 2071 again, so that the multi-directional vibration of the shell 2071 can effectively reduce bubbles, and the baseline can be stabilized by eliminating bubbles, so that the analysis result is more stable.
[0050] Example 3: Reference Figure 2-Figure 5A device for detecting purity of emamectin benzoate includes a built-in detection auxiliary mechanism 200, which includes an external support component 201 and a conveying component 207. A driving component 202 is assembled in the middle of the external support component 201, and a transmission component 204 is arranged below the driving component 202. The transmission component 204 passes through the conveying component 207 and is connected to a vibration component 205. The vibration component 205 is located below the conveying component 207. Four stirring components 206 are arranged inside the conveying component 207, and one end of the four stirring components 206 is transmitted to the transmission component 204. Four elastic components 203 are arranged outside the conveying component 207, and the four elastic components 203 are arranged on the external support component 201.
[0051] In this embodiment: by rotating the driving component 202, the eccentric movement of the eccentric disk 2023 can cooperate with the elastic component 203 to realize the vibration of the outer shell 2071. At the same time, the driving component 202 drives the transmission component 204 to rotate, and the transmission component 204 and the stirring component 206 transmit, so that the stirring component 206 rotates. At the same time, the transmission component 204 drives the vibration component 205 to rotate, so that the vibration component 205 and the conveying component 207 produce an extrusion movement, and cooperate with the elastic component 203 to realize the multi-directional vibration of the outer shell 2071. The multi-directional vibration and the stirring component 206 can improve the uniformity of mixing and heating of the emamectin benzoate sample, and help degas and exhaust the mobile phase, so as to greatly reduce the influence of bubbles on chromatographic separation and improve the separation effect. Moreover, this method is simple to operate and has low cost.
[0052] A method for using an emamectin benzoate purity detection device comprises the following steps:
[0053] S1. When the purity of emamectin benzoate is detected, the transmission shaft 2025 is driven to rotate by the motor 2022, so that the transmission shaft 2025 drives the eccentric disk 2023 to rotate, and the rotation of the eccentric disk 2023 drives the transmission assembly 204 to rotate, so that the housing 2071 follows the movement. Due to the eccentric movement of the eccentric disk 2023, the eccentric disk 2023 cooperates with the first spring 2034 to realize the vibration of the housing 2071;
[0054] S2. When the gear 2041 moves following the eccentric disk 2023, the gear 2041 and the gear ring 2024 are transmitted, the gear 2041 drives the polygonal shaft 2042 to rotate, the polygonal shaft 2042 drives the chassis 2051 to rotate, the chassis 2051 drives the ball 2052 to move, so that the ball 2052 and the convex ball 2076 produce a squeezing movement, so that the housing 2071 moves, and the ball 2052 cooperates with the second spring 2032 and the third spring 2053 to realize the vibration of the housing 2071. The above operation makes the housing 2071 vibrate in multiple directions;
[0055] S3. When the polygonal shaft 2042 rotates, the polygonal shaft 2042 drives the inner sleeve 2043 to rotate, the inner sleeve 2043 drives the outer sleeve 2044 to rotate, the outer sleeve 2044 drives the first bevel gear 2045 to rotate, the first bevel gear 2045 and the second bevel gear 2062 drive, the second bevel gear 2062 drives the rotating shaft 2063 to rotate, and the rotating shaft 2063 drives the stirring blade 2061 to rotate;
[0056] S4. The emamectin benzoate sample is then transported downward through the top of the liquid chromatograph 100, so that the emamectin benzoate sample enters the spiral path 2073 from the connecting tube 2072, and the outer shell 2071 vibrates in multiple directions to eliminate bubbles in the emamectin benzoate sample, so that the emamectin benzoate sample is spirally transported along the spiral path 2073, and at the same time is heated by the heating plate 2074 and stirred multiple times by the stirring blade 2061, and then enters the bottom of the liquid chromatograph 100 through the connecting tube 2072 to detect the purity of the emamectin benzoate sample.
[0057] The above are only preferred specific implementation modes of the present invention, but the protection scope of the present invention is not limited thereto. Any technician familiar with the technical field can make equivalent replacements or changes according to the technical solutions and inventive concepts of the present invention within the technical scope disclosed by the present invention, which should be covered by the protection scope of the present invention.
Claims
1. A device for detecting purity of emamectin benzoate, comprising a liquid chromatograph (100), characterized in that: A cavity (101) is provided in the upper middle portion of the liquid chromatograph (100), and a built-in detection auxiliary mechanism (200) is installed inside the cavity (101); The built-in detection auxiliary mechanism (200) comprises an external support component (201) and a conveying component (207); a driving component (202) is mounted in the middle of the external support component (201); a transmission component (204) is arranged below the driving component (202); the transmission component (204) passes through the conveying component (207) and is connected to the vibration component (205); the vibration component (205) is located below the conveying component (207); four stirring components (206) are arranged inside the conveying component (207); one end of the four stirring components (206) is transmitted to the transmission component (204); four elastic components (203) are arranged outside the conveying component (207); the four elastic components (203) are arranged in the external support component (201); The external support assembly (201) comprises a support frame (2011), four first slide grooves (2015) are provided inside the support frame (2011), support columns (2012) are installed at four corners of the support frame (2011), a reinforcement rod (2014) is fixedly connected to the top of the support column (2012), and a mounting plate (2013) is fixedly connected to the upper and lower ends of the support column (2012), and the mounting plate (2013) is fixedly connected in the cavity (101); The conveying assembly (207) comprises a shell (2071), the exterior of the shell (2071) is provided with four second slide grooves (2075), and the bottom of the shell (2071) is fixedly connected with a plurality of convex balls (2076) arranged in an annular manner; A spiral track (2073) is provided inside the shell (2071), and a plurality of heating plates (2074) are installed inside the spiral track (2073), a gap is reserved between the heating plates (2074) and the inner wall of the spiral track (2073), and every three heating plates (2074) are staggered; Both sides of the housing (2071) are provided with connecting pipes (2072), the connecting pipes (2072) are hoses, and one end of the two connecting pipes (2072) is connected to the liquid chromatograph (100); The stirring assembly (206) comprises a rotating shaft (2063), the rotating shaft (2063) being arranged to cross the spiral track (2073), the rotating shaft (2063) being rotatably mounted on the side wall of the spiral track (2073) via a plurality of bearings, a plurality of stirring blades (2061) being fixedly connected to the outside of the rotating shaft (2063), and a second bevel gear (2062) being fixedly connected to one end of the rotating shaft (2063).
2. A emamectin benzoate purity detection device according to claim 1, characterized in that, The driving assembly (202) comprises a fixing frame (2021), the fixing frame (2021) being fixedly connected to four reinforcing rods (2014), a gear ring (2024) being fixedly connected below the fixing frame (2021), a motor (2022) being installed in the middle of the fixing frame (2021), an output shaft of the motor (2022) being fixedly connected to a transmission shaft (2025), and an eccentric disk (2023) being fixedly connected to the bottom end of the transmission shaft (2025).
3. A kind of emamectin benzoate purity detection device according to claim 2, characterized in that, The transmission assembly (204) comprises a polygonal shaft (2042), wherein the polygonal shaft (2042) is rotatably mounted on an eccentric disk (2023) via a bearing, and a gear (2041) is fixedly connected to the top end of the polygonal shaft (2042), wherein the gear (2041) meshes with a gear ring (2024).
4. A emamectin benzoate purity detection device according to claim 3, characterized in that, The outer sleeve of the polygonal shaft (2042) is provided with an inner sleeve (2043); the outer portion of the inner sleeve (2043) is fixedly connected to an outer sleeve (2044); the outer sleeve (2044) is rotatably mounted on the outer shell (2071) via two bearings; a first bevel tooth (2045) is fixedly connected to the outer sleeve (2044); the first bevel tooth (2045) is meshed with four second bevel teeth (2062).
5. A emamectin benzoate purity detection device according to claim 4, characterized in that, The vibration assembly (205) comprises a chassis (2051), a plurality of balls (2052) are fixedly connected to the top of the chassis (2051), the arrangement of the balls (2052) is the same as that of the convex balls (2076), and the balls (2052) are in contact with the convex balls (2076), and a third spring (2053) is fixedly connected to the top of the chassis (2051), and the third spring (2053) is fixedly connected to the bottom of the inner shaft sleeve (2043).
6. A emamectin benzoate purity detection device according to claim 5, characterized in that, The elastic component (203) comprises a first slider (2036), the first slider (2036) slides in a first slide groove (2015), one side of the first slider (2036) is fixedly connected to two telescopic rods (2035) and two first springs (2034), one end of the two telescopic rods (2035) and the two first springs (2034) is fixedly connected to a connecting plate (2031), one side of the connecting plate (2031) is fixedly connected to a second slider (2033), the second slider (2033) slides in a second slide groove (2075), and a second spring (2032) is fixedly connected between the bottom of the second slider (2033) and the bottom wall of the second slide groove (2075).
7. The method for using the emamectin benzoate purity detection device according to claim 6, characterized in that: The following steps are involved: S1. When the purity of emamectin benzoate is detected, the transmission shaft (2025) is driven to rotate by the motor (222), so that the transmission shaft (2025) drives the eccentric disk (2023) to rotate, and the rotation of the eccentric disk (2023) drives the transmission assembly (204) to rotate, so that the housing (2071) follows the movement. Due to the eccentric movement of the eccentric disk (2023), the eccentric disk (2023) cooperates with the first spring (2034) to achieve vibration of the housing (2071); S2. When the gear (2041) moves following the eccentric disk (2023), the gear (2041) and the gear ring (2024) are driven, the gear (2041) drives the polygonal shaft (2042) to rotate, the polygonal shaft (2042) drives the chassis (2051) to rotate, the chassis (2051) drives the ball (2052) to move, so that a squeezing movement is generated between the ball (2052) and the convex ball (2076), so that the housing (2071) moves, so that the ball (2052) cooperates with the second spring (2032) and the third spring (2053) to achieve vibration of the housing (2071), and the above operations cause the housing (2071) to vibrate in multiple directions; S3. When the polygonal shaft (2042) rotates, the polygonal shaft (2042) drives the inner shaft sleeve (2043) to rotate, the inner shaft sleeve (2043) drives the outer shaft sleeve (2044) to rotate, the outer shaft sleeve (2044) drives the first bevel gear (2045) to rotate, the first bevel gear (2045) and the second bevel gear (2062) are driven, the second bevel gear (2062) drives the rotating shaft (2063) to rotate, and the rotating shaft (2063) drives the stirring blade (2061) to rotate; S4. The emamectin benzoate sample is then transported downward through the top of the liquid chromatograph (100), so that the emamectin benzoate sample enters the spiral path (2073) from the connecting tube (2072), and the outer shell (2071) vibrates in multiple directions to eliminate bubbles in the emamectin benzoate sample, so that the emamectin benzoate sample is spirally transported along the spiral path (2073), and is heated by the heating plate (2074) and stirred multiple times by the stirring blade (2061), and then enters the bottom of the liquid chromatograph (100) through the connecting tube (2072) to detect the purity of the emamectin benzoate sample.
Citation Information
Patent Citations
High performance liquid chromatograph convenient for feeding
CN221326427U