A preparation and detection collector for vitamin C microcapsules
Patent Information
- Application Number
- CN202522168446.1
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2025-10-14
- Publication Date
- 2026-09-22
- Estimated Expiration
- 2035-10-14
AI Technical Summary
[0005]有鉴于此,本实用新型提供了一种维生素C微胶囊的制备检测采集器,能够解决现有技术中维生素C微胶囊制备过程缺乏实时检测和采集手段,导致制备质量难以控制和产品一致性差的问题
[0027]采用上述改进方案的有益效果为:12个散热肋片的数量设置经过优化计算,既保证了充分的散热效果,又避免了过多肋片导致的制造成本增加。沿圆周方向均匀分布的布置方式确保了散热的均匀性,防止了局部温度梯度的形成,为维生素C微胶囊的稳定制备创造了理想的温度环境条件。
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Figure CN224788303U_ABST
Abstract
Description
Technical Field
[0001] This invention belongs to the field of pharmaceutical preparation detection technology, and specifically relates to a sampler for the preparation and detection of vitamin C microcapsules. Background Technology
[0002] Vitamin C, an essential water-soluble vitamin for the human body, has important physiological functions such as anti-oxidation and enhancing immunity, and is widely used in food additives, nutritional supplements and pharmaceutical preparations.
[0003] However, vitamin C is chemically unstable and easily decomposes and becomes ineffective due to factors such as light, heat, oxygen, and metal ions, severely limiting its effectiveness in practical applications. To improve the stability and bioavailability of vitamin C, microencapsulation technology has emerged. Microencapsulation involves encapsulating vitamin C in tiny capsules formed from polymeric materials, using physical barriers to protect the core substance from adverse environmental influences.
[0004] Currently, the industrial preparation of vitamin C microcapsules mainly employs processes such as spray drying, coagulation, and interfacial polymerization. Existing preparation equipment typically separates preparation and testing, requiring periodic shutdowns for sampling and testing during the preparation process. This is not only inefficient but also makes real-time quality control difficult due to the lag in testing. Traditional stirring devices often use simple paddle structures, resulting in limited mixing effects and the creation of dead zones that negatively impact microcapsule formation quality. Temperature control systems often lack precision, exhibiting significant temperature fluctuations that adversely affect the stability of vitamin C. Sampling devices are usually manually operated, leading to uneven sampling and a high risk of contamination. Utility Model Content
[0005] In view of this, the present invention provides a detection and acquisition device for the preparation of vitamin C microcapsules, which can solve the problem that the lack of real-time detection and acquisition methods in the preparation process of vitamin C microcapsules in the prior art leads to difficulty in controlling the preparation quality and poor product consistency.
[0006] This utility model is implemented as follows:
[0007] This invention provides a preparation and detection collection device for vitamin C microcapsules, comprising a preparation reactor, a detection and collection device, a support base, a transmission mechanism, and a temperature control system. The support base is a rectangular steel frame structure, with the preparation reactor fixedly installed at the center. The preparation reactor has a cylindrical structure and its axis is perpendicular to the plane of the support base. A feeding port is provided at the top of the preparation reactor, and a sealing cover is installed at the feeding port. The detection and collection device is installed on the side wall of the preparation reactor and includes a detection and collection device body, a rotating collection arm, and a collection pipeline. The detection and collection device body is cylindrical and fixed to the middle of the side wall of the preparation reactor via a flange connection. The rotating collection arm is rotatably installed inside the detection and collection body via a bearing assembly. One end of the rotating collection arm extends to the center of the inner cavity of the preparation reactor, and the other end is connected to the collection pipeline. The transmission mechanism is installed on one side of the support base and includes a drive motor and a reducer. The output shaft of the drive motor is connected to the input end of the reducer via a coupling, and the output end of the reducer is connected to the outer end of the rotating collection arm via a transmission shaft.
[0008] The technical advantages of the vitamin C microcapsule preparation detection and collection device provided by this utility model are as follows: Through the integrated design of the preparation reactor and the detection and collection device, real-time detection and collection during the vitamin C microcapsule preparation process are achieved, avoiding the time delay problem caused by traditional separate detection. The rotational movement of the collection arm inside the preparation reactor allows for sample collection at different positions, ensuring the representativeness and uniformity of the sampling. The transmission mechanism provides stable speed control through a reducer, ensuring the accuracy of the collection process, while the integrated design of the temperature control system provides a stable temperature environment for microcapsule preparation.
[0009] Based on the above technical solution, the vitamin C microcapsule preparation detection and collection device of this utility model can be further improved as follows:
[0010] The reactor has spiral stirring blades on its inner wall. The spiral stirring blades are spirally distributed along the inner wall of the reactor. The spiral angle of the spiral stirring blades is 30 to 60 degrees. The spiral stirring blades are fixed to the inner wall of the reactor by welding.
[0011] The beneficial effects of adopting the above-mentioned improved scheme are as follows: the design of the helical stirring blades can form a three-dimensional stirring flow field inside the preparation reactor, improving the mixing uniformity of vitamin C solution and encapsulation material. The helical angle, set within the range of 30 to 60 degrees, ensures sufficient stirring while avoiding excessive shearing that could damage the microcapsule structure. The distribution of the helical stirring blades along the inner wall effectively prevents the formation of dead zones, ensuring a uniform reaction throughout the entire system.
[0012] Furthermore, the detection and acquisition device also includes a filter screen and a buffer storage chamber. The filter screen is located at the front end of the rotating acquisition arm and has a conical stainless steel wire mesh structure with a mesh diameter of 50 to 100 micrometers. The buffer storage chamber is located inside the detection and acquisition body and is connected to the acquisition pipeline. The volume of the buffer storage chamber is 100 to 200 milliliters.
[0013] The beneficial effects of adopting the above-mentioned improved scheme are as follows: the conical design of the filter screen increases the filtration area and improves the filtration efficiency; at the same time, the mesh diameter of 50 to 100 micrometers can effectively separate microcapsule particles that meet the requirements. The buffer reservoir provides temporary storage space for sample collection, avoiding the impact of pressure fluctuations in the collection pipeline on sample quality. The 100 to 200 ml volume design meets the detection needs while avoiding sample retention problems caused by excessive volume.
[0014] Furthermore, the temperature control system includes a heating sleeve, a temperature sensor, and a temperature controller. The heating sleeve surrounds the outer wall of the preparation reactor and is fixed by a clamp. The heating sleeve contains a resistance wire heating element. The temperature sensor is installed on the side wall of the preparation reactor and its probe extends into the inner cavity of the preparation reactor. The temperature sensor is connected to the temperature controller via a cable.
[0015] The beneficial effects of the above-mentioned improved scheme are as follows: the design of the heating sleeve surrounding the outer wall of the reactor achieves uniform heating and avoids local overheating. The built-in design of the resistance wire heating element improves heat transfer efficiency and shortens heating time. The arrangement of the temperature sensor probe extending into the reactor cavity enables real-time monitoring of the actual temperature of the reaction system, and through linkage with the temperature controller, achieves precise temperature control, providing a reliable guarantee for the stable preparation of vitamin C microcapsules.
[0016] Furthermore, the rotating collection arm has an L-shaped structure, with the horizontal section being 2 / 3 the length of the inner diameter of the preparation reactor and the vertical section being 1 / 3 the height of the preparation reactor; the cross-section of the rotating collection arm is circular with a diameter of 8 mm to 12 mm.
[0017] The beneficial effects of adopting the above-mentioned improved scheme are as follows: The L-shaped rotating sampling arm design makes full use of the three-dimensional space inside the reactor, and the horizontal section length of 2 / 3 of the inner diameter ensures that the sampling range covers the main area of the reactor. The vertical section length of 1 / 3 of the height allows for sampling at different liquid levels. The circular cross-sectional diameter of 8 mm to 12 mm ensures the structural strength of the sampling arm while reducing disturbance to the flow field of the reaction system and improving the representativeness of the collected samples.
[0018] Furthermore, the support base includes four support legs and a connecting beam. The four support legs are rectangularly distributed and bolted to the four corners of the connecting beam. Each support leg has a height-adjustable spiral adjustment foot at its bottom. The connecting beam is an I-beam structure with a circular mounting hole in the center. The preparation reactor is fixed in the circular mounting hole by a flange.
[0019] The beneficial effects of adopting the above-mentioned improved design are as follows: the rectangular distribution of the four support legs provides a stable support foundation, effectively resisting vibrations and torques generated during equipment operation. The height-adjustable spiral feet can adapt to different ground conditions, ensuring horizontal installation of the equipment. The connecting beams of the I-beam structure have high strength and rigidity, capable of bearing the weight of the preparation reactor and its contents. The matching design of the central circular mounting hole and flange enables precise positioning and reliable fixation of the preparation reactor.
[0020] Furthermore, the outer wall of the reactor is provided with multiple heat dissipation fins, which are distributed at equal intervals along the axial direction of the reactor.
[0021] The beneficial effects of adopting the above-mentioned improved scheme are as follows: the design of multiple heat dissipation fins evenly distributed along the axial direction increases the heat dissipation area of the preparation reactor, improves heat dissipation efficiency, and effectively prevents excessive temperature accumulation during the reaction process. The heat dissipation fins help maintain the temperature stability of the reaction system, avoid the adverse effects of temperature fluctuations on the quality of vitamin C microcapsules, and extend the service life of the equipment.
[0022] Furthermore, the inner wall of the detection and acquisition body is provided with an annular guide groove, the depth of which is 2 mm to 5 mm.
[0023] The beneficial effects of adopting the above-mentioned improved scheme are as follows: the annular guide groove design on the inner wall of the sampling body can guide the collected fluid to form a regular flow path, reducing the generation of turbulence. The groove depth of 2 mm to 5 mm can effectively guide the flow without significantly affecting the overall strength of the sampling body. The annular guide groove helps to improve the sampling efficiency and reduce sample residue during the sampling process.
[0024] Furthermore, the upper surface of the sealing cover is provided with raised reinforcing ribs, which are distributed in a cross shape.
[0025] The beneficial effects of adopting the above-mentioned improved scheme are as follows: the design of the cross-shaped reinforcing ribs on the upper surface of the sealing cover plate significantly improves the bending strength and deformation resistance of the cover plate, enabling it to withstand the pressure inside the reactor. The raised reinforcing rib structure also enhances the sealing effect between the sealing cover plate and the feeding port, preventing leakage of the reaction system, while facilitating cleaning and maintenance.
[0026] Furthermore, there are 12 heat dissipation fins, which are evenly distributed along the circumference on the outer wall of the reactor.
[0027] The beneficial effects of adopting the above-mentioned improved scheme are as follows: the number of 12 heat dissipation fins has been optimized through calculation, ensuring sufficient heat dissipation while avoiding increased manufacturing costs caused by too many fins. The uniform distribution along the circumference ensures uniform heat dissipation, prevents the formation of local temperature gradients, and creates ideal temperature environment conditions for the stable preparation of vitamin C microcapsules.
[0028] Compared with existing technologies, the beneficial effects of the vitamin C microcapsule preparation detection and collection device provided by this utility model are as follows: Through the integrated design of the preparation reactor and the detection and collection device, real-time monitoring and sample collection of the vitamin C microcapsule preparation process are achieved, effectively solving the problems of detection lag and quality control difficulties in traditional preparation processes. The three-dimensional collection capability of the rotating collection arm ensures sample representativeness, the optimized design of the spiral stirring blades improves mixing uniformity, and the precise control of the temperature control system provides a stable temperature environment for the reaction. The filter screen and buffer storage chamber enable sample pretreatment and temporary storage, and the stable structure of the support base ensures the reliability of equipment operation. The coordinated operation of the entire device not only improves the preparation efficiency and product quality of vitamin C microcapsules but also provides a reliable technical means for industrial production. Compared with existing technologies, this utility model has significant advantages such as reasonable structure, simple operation, accurate detection, and stable control, and can meet the high standards of modern food and pharmaceutical industries for vitamin C microcapsule product quality. Attached Figure Description
[0029] To more clearly illustrate the technical solutions of the embodiments of this utility model, the drawings used in the description of the embodiments of this utility model will be briefly introduced below. Obviously, the drawings described below are only some embodiments of this utility model. For those skilled in the art, other drawings can be obtained based on these drawings without creative effort.
[0030] Figure 1 A three-dimensional structural diagram of a detection and acquisition device for the preparation of vitamin C microcapsules;
[0031] Figure 2 A side view of a sampler for the preparation and detection of vitamin C microcapsules;
[0032] Figure 3 This is a schematic diagram of the internal structure of the reactor.
[0033] The attached diagram lists the components represented by each number as follows:
[0034] 10. Preparation reactor; 11. Detection and collection device; 12. Support base; 13. Transmission mechanism; 14. Temperature control system; 15. Feed port; 16. Sealing cover; 17. Rotary collection arm; 18. Collection pipeline; 19. Drive motor; 20. Reducer; 21. Filter screen; 22. Buffer storage chamber; 23. Heating sleeve; 24. Support leg; 25. Connecting crossbeam. Detailed Implementation
[0035] To make the objectives, technical solutions, and advantages of the embodiments of this utility model clearer, the technical solutions of the embodiments of this utility model will be clearly and completely described below with reference to the accompanying drawings.
[0036] like Figure 1-3 The image shows an embodiment of a vitamin C microcapsule preparation and detection collection device provided by this utility model. In this embodiment, it includes a preparation reactor 10, a detection and collection device 11, a support base 12, a transmission mechanism 13, and a temperature control system 14. The support base is a rectangular steel frame structure, with the preparation reactor fixedly installed at the center. The preparation reactor has a cylindrical structure, and its axis is perpendicular to the plane of the support base. A feeding port 15 is provided at the top of the preparation reactor, and a sealing cover 16 is installed at the feeding port. The detection and collection device is installed on the side wall of the preparation reactor and includes… The detection and acquisition device consists of a main body, a rotating acquisition arm 17, and an acquisition pipeline 18. The main body is cylindrical and fixed to the middle of the side wall of the preparation reactor via a flange connection. The rotating acquisition arm is rotatably mounted inside the main body via a bearing assembly. One end of the rotating acquisition arm extends to the center of the inner cavity of the preparation reactor, and the other end is connected to the acquisition pipeline. A transmission mechanism is installed on one side of the support base. The transmission mechanism includes a drive motor 19 and a reducer 20. The output shaft of the drive motor is connected to the input end of the reducer via a coupling, and the output end of the reducer is connected to the outer end of the rotating acquisition arm via a transmission shaft.
[0037] In the above technical solution, the inner wall of the preparation reactor is provided with spiral stirring blades, which are spirally distributed along the inner wall of the preparation reactor. The spiral angle of the spiral stirring blades is 30 degrees to 60 degrees, and the spiral stirring blades are fixed to the inner wall of the preparation reactor by welding.
[0038] Furthermore, in the above technical solution, the detection and acquisition device also includes a filter screen 21 and a buffer storage chamber 22. The filter screen is located at the front end of the rotating acquisition arm and has a conical stainless steel wire mesh structure with a mesh diameter of 50 micrometers to 100 micrometers. The buffer storage chamber is located inside the detection and acquisition body and is connected to the acquisition pipeline. The volume of the buffer storage chamber is 100 ml to 200 ml.
[0039] Furthermore, in the above technical solution, the temperature control system includes a heating sleeve 23, a temperature sensor, and a temperature controller. The heating sleeve surrounds the outer wall of the preparation reactor and is fixed by a clamp. The heating sleeve is equipped with a resistance wire heating element. The temperature sensor is installed on the side wall of the preparation reactor and the probe extends into the inner cavity of the preparation reactor. The temperature sensor is connected to the temperature controller via a cable.
[0040] Furthermore, in the above technical solution, the rotating collection arm has an L-shaped structure, the length of the horizontal section of the L-shaped structure is 2 / 3 of the inner diameter of the preparation reactor, and the length of the vertical section is 1 / 3 of the height of the preparation reactor; the cross-section of the rotating collection arm is circular, with a diameter of 8 mm to 12 mm.
[0041] Furthermore, in the above technical solution, the support base includes four support legs 24 and a connecting beam 25. The four support legs are rectangularly distributed and connected to the four corners of the connecting beam by bolts. Each support leg has a height-adjustable spiral adjustment foot at its bottom. The connecting beam is an I-beam structure with a circular mounting hole in the center. The preparation reactor is fixed in the circular mounting hole by a flange.
[0042] Furthermore, in the above technical solution, the outer wall of the reactor is provided with multiple heat dissipation fins, which are distributed at equal intervals along the axial direction of the reactor.
[0043] Furthermore, in the above technical solution, the inner wall of the detection and acquisition body is provided with an annular guide groove, the depth of which is 2 mm to 5 mm.
[0044] Furthermore, in the above technical solution, the upper surface of the sealing cover is provided with raised reinforcing ribs, which are distributed in a cross shape.
[0045] Furthermore, in the above technical solution, the number of heat dissipation fins is 12, and the heat dissipation fins are evenly distributed along the circumferential direction on the outer wall of the reactor.
[0046] The following is a specific embodiment 1 of this utility model: The vitamin C microcapsule preparation detection and collection device in this embodiment is mainly used for the preparation of pharmaceutical-grade vitamin C microcapsules. The support base is welded from Q235 carbon steel, and has a rectangular frame structure with dimensions of 2000 mm in length, 1500 mm in width, and 800 mm in height. The four support legs have a pipe diameter of 100 mm and a wall thickness of 8 mm, and are fixedly connected to the connecting beam by M16 bolts. The connecting beam is made of 300 mm high I-beams, with a circular mounting hole with a diameter of 600 mm in the center. The spiral adjusting foot installed at the bottom of each support leg has a stroke of 50 mm, and the base diameter is 120 mm. The preparation reactor is made of 316L stainless steel, with an inner diameter of 500 mm, a height of 800 mm, a wall thickness of 10 mm, and a volume of approximately 160 liters. The bottom of the reactor is an elliptical head, and the top has a feeding port with an inner diameter of 100 mm. The spiral stirring blades are made of stainless steel plate, with a thickness of 3 mm, a width of 80 mm, a spiral angle of 45 degrees, and are distributed in a double spiral along the inner wall of the reactor. The sealing cover is 120 mm in diameter and 15 mm thick, with a cross-shaped reinforcing rib on the upper surface that is 8 mm high and 15 mm wide. The detection and collection device has an inner diameter of 80 mm and a length of 200 mm, and is connected to the reactor sidewall via a DN80 flange. The rotating collection arm is made of stainless steel tubing with an outer diameter of 10 mm and a wall thickness of 1.5 mm. The horizontal section of the L-shaped structure is 350 mm long, and the vertical section is 250 mm long. The filter screen is made of 80-mesh stainless steel wire mesh, with a conical structure having a top diameter of 20 mm, a bottom diameter of 40 mm, and a height of 60 mm. The buffer storage chamber has a volume of 150 ml and is made of transparent plexiglass for easy observation. The drive motor in the transmission mechanism has a power of 2.2 kW and a speed of 1440 rpm, with a reducer ratio of 40:1 and an output speed of 36 rpm. The heating sleeve of the temperature control system is made of stainless steel and houses a 6 kW resistance wire heating element. The temperature sensor uses a PT100 resistance thermometer, with a temperature range of 0 to 200 degrees Celsius and an accuracy of ±0.5 degrees Celsius. The temperature controller has a PID control function, with a temperature control accuracy of ±2 degrees Celsius. The outer wall heat dissipation fins are 20 mm high, 5 mm thick, and 400 mm long, evenly distributed along the axial direction at 60 mm intervals. In the actual preparation process, gum arabic solution and gelatin solution were used as encapsulation materials, the vitamin C solution concentration was 20%, the preparation temperature was controlled at 55 degrees Celsius, the stirring speed was 25 rpm, and the reaction time was 2 hours. The sampling arm rotated at 2 rpm, and samples were collected every 30 minutes for analysis. The temperature fluctuation throughout the preparation process was controlled within ±1 degree Celsius, the product had good particle size uniformity, and the encapsulation rate reached over 85%, meeting the quality requirements of pharmaceutical-grade vitamin C microcapsules.
[0047] The following is another specific embodiment 2 of this utility model: This embodiment is an optimization and improvement on the preparation of food-grade vitamin C microcapsules based on Embodiment 1. The volume of the preparation reactor is increased to 300 liters, the inner diameter is increased to 650 mm, and the height is adjusted to 900 mm to meet the needs of mass production. The spiral stirring blades adopt a triple spiral distribution, the spiral angle is adjusted to 35 degrees, and the blade width is increased to 100 mm to improve stirring efficiency. The rotating collection arm is changed to a double-arm structure, with two L-shaped collection arms symmetrically distributed at 180 degrees, the horizontal section length is increased to 450 mm, and the vertical section length is 300 mm, allowing for simultaneous collection of samples from more locations. The filter screen is adjusted to 100 mesh to adapt to the different particle size requirements of food-grade products. The volume of the buffer storage chamber is increased to 250 ml and made of 316L stainless steel, meeting food safety standards. The power of the drive motor of the transmission mechanism is increased to 4 kW, the speed ratio of the reducer is adjusted to 60:1, and the output speed is 24 rpm. The temperature control system's heating power was increased to 10 kW, and two temperature sensors were installed to monitor the temperature at the top and bottom of the reactor respectively, ensuring a more uniform temperature field. The number of heat dissipation fins was increased to 16, and their height was adjusted to 30 mm to enhance heat dissipation. In terms of the preparation process, sodium alginate and chitosan were used as embedding materials, the vitamin C solution concentration was adjusted to 15%, the preparation temperature was controlled at 50 degrees Celsius, the stirring speed was 20 rpm, and the reaction time was extended to 3 hours. A dual-arm sampling system collects samples every 20 minutes, resulting in a higher detection frequency and more precise quality control.
[0048] The following is another specific embodiment 3 of this utility model: This embodiment is an upgrade and improvement based on Embodiment 1, with the addition of automated control functions. A control cabinet is added to the support base, housing a PLC controller and a human-machine interface to achieve automated operation of the equipment. A liquid level sensor and a pressure sensor are added to the preparation reactor to monitor the state of the reaction system in real time. A flow sensor is configured in the detection and acquisition device to precisely control the flow rate and volume of the collected samples. The transmission mechanism is controlled by a frequency converter, which can precisely adjust the stirring speed and the acquisition arm speed according to process requirements. The temperature control system is upgraded to multi-point temperature monitoring, with six temperature sensors installed on the reactor wall to form a temperature monitoring network. Combined with zoned control of heating power, more precise temperature management is achieved. A safety interlock system is added, automatically shutting down for protection when parameters such as temperature, pressure, and liquid level exceed the set range. An automatic cleaning function is added to the detection and acquisition pipeline, automatically flushing the pipeline after each acquisition to prevent cross-contamination. The control system has data recording and report generation functions, automatically recording various process parameters and detection data during the preparation process and generating batch production records. The human-machine interface uses a 10.4-inch color touchscreen, with a user-friendly and intuitive interface, making process parameter settings and monitoring clear at a glance. The application of the entire automation system has greatly improved the ease of operation and production efficiency of the equipment, reduced human error, and ensured the stability and consistency of product quality.
[0049] The operating method of this utility model is as follows: First, install and debug the entire set of equipment to ensure that the support base is level and stable and that all components are tightly and reliably connected. Before starting the machine, check that the electrical wiring is correctly connected, the transmission mechanism is well lubricated, and the temperature control system is working normally. Prepare the required vitamin C solution and embedding material according to the formula ratio. Start the temperature control system, set the required reaction temperature value, and start the feeding operation after the temperature inside the preparation reactor reaches the set value. Add the embedding material and vitamin C solution sequentially through the feeding port, and cover the sealing cover after feeding is completed. Start the transmission mechanism and adjust the speed to a suitable range so that the spiral stirring blades start stirring and mixing. At the same time, start the detection and acquisition device, and the rotating acquisition arm starts to rotate and collect samples inside the reactor. During the preparation process, the temperature sensor monitors the reaction temperature in real time, and the temperature controller automatically adjusts the heating power to maintain a stable temperature. After the collected sample is filtered through a filter screen, it enters the buffer storage chamber and is then transported to external detection equipment through the collection pipeline for quality testing such as particle size analysis and embedding rate determination. Adjust the preparation process parameters in real time according to the test results, such as stirring speed, reaction temperature, and material ratio, to ensure that the product quality meets the requirements. After preparation, heating and stirring are stopped. Once the temperature inside the reactor has dropped to a safe range, the unloading operation begins, transferring the prepared vitamin C microcapsules to subsequent processing steps. After use, the equipment is cleaned and maintained to prepare it for the next use.
[0050] Specifically, the principle of this invention is as follows: Through the integrated design of the preparation reactor and the detection and acquisition device, sample detection and acquisition are performed simultaneously during the preparation of vitamin C microcapsules. The spiral stirring blades inside the preparation reactor, driven by a transmission mechanism, generate a three-dimensional stirring flow field, ensuring thorough mixing of the vitamin C solution and the embedding material, promoting uniform microcapsule formation. The temperature control system provides a uniform temperature field through a heating sleeve, a temperature sensor monitors the reaction temperature in real time, and a temperature controller automatically adjusts the heating power according to the set value to maintain the optimal temperature conditions required for the preparation process. The rotating acquisition arm in the detection and acquisition device rotates slowly under the drive of a reduction transmission system, collecting samples at different locations within the reactor. Microcapsule particles meeting the particle size requirements are initially separated through a filter screen. The collected samples are first temporarily stored in a buffer storage chamber to avoid the impact of pipeline pressure fluctuations on sample quality, and then transported to external detection equipment for further analysis through the acquisition pipeline. The support base provides a stable foundation for the entire device; the rectangular distribution of the four support legs effectively resists vibration and torque during operation, and the height-adjustable spiral feet ensure horizontal installation of the equipment. The coordinated operation of the entire system enables continuous monitoring and quality control of the preparation process, significantly improving the preparation efficiency and product consistency of vitamin C microcapsules.
Claims
1. A detection and collection device for the preparation of vitamin C microcapsules, characterized in that, The system includes a preparation reactor, a detection and acquisition device, a support base, a transmission mechanism, and a temperature control system. The support base is a rectangular steel frame structure, with the preparation reactor fixedly installed in the center. The preparation reactor has a cylindrical structure, and its axis is perpendicular to the plane of the support base. The top of the preparation reactor has a feeding port, which is fitted with a sealing cover. The detection and acquisition device is installed on the side wall of the preparation reactor. The detection and acquisition device includes a device body, a rotating acquisition arm, and acquisition pipeline. The device body is cylindrical and fixed to the middle of the side wall of the preparation reactor via a flange connection. The rotating acquisition arm is rotatably installed inside the detection and acquisition body via a bearing assembly. One end of the rotating acquisition arm extends to the center of the inner cavity of the preparation reactor, and the other end is connected to the acquisition pipeline. The transmission mechanism is installed on one side of the support base. The transmission mechanism includes a drive motor and a reducer. The output shaft of the drive motor is connected to the input end of the reducer via a coupling, and the output end of the reducer is connected to the outer end of the rotating acquisition arm via a transmission shaft.
2. The vitamin C microcapsule preparation detection and collection device according to claim 1, characterized in that, The inner wall of the preparation reactor is equipped with helical stirring blades, which are spirally distributed along the inner wall of the preparation reactor. The spiral angle of the helical stirring blades is 30 degrees to 60 degrees. The helical stirring blades are fixed to the inner wall of the preparation reactor by welding.
3. The vitamin C microcapsule preparation detection and collection device according to claim 2, characterized in that, The detection and acquisition device also includes a filter screen and a buffer storage chamber. The filter screen is located at the front end of the rotating acquisition arm. The filter screen has a conical stainless steel wire mesh structure with a mesh diameter of 50 micrometers to 100 micrometers. The buffer storage chamber is located inside the detection and acquisition body and is connected to the acquisition pipeline. The volume of the buffer storage chamber is 100 ml to 200 ml.
4. The vitamin C microcapsule preparation detection and collection device according to claim 3, characterized in that, The temperature control system includes a heating sleeve, a temperature sensor, and a temperature controller. The heating sleeve surrounds the outer wall of the preparation reactor and is fixed by a clamp. The heating sleeve contains a resistance wire heating element. The temperature sensor is installed on the side wall of the preparation reactor and the probe extends into the inner cavity of the preparation reactor. The temperature sensor is connected to the temperature controller via a cable.
5. The vitamin C microcapsule preparation detection and collection device according to claim 4, characterized in that, The rotating collection arm has an L-shaped structure. The length of the horizontal section of the L-shaped structure is 2 / 3 of the inner diameter of the preparation reactor, and the length of the vertical section is 1 / 3 of the height of the preparation reactor. The cross-section of the rotating collection arm is circular, with a diameter of 8 mm to 12 mm.
6. The vitamin C microcapsule preparation detection and collection device according to claim 5, characterized in that, The support base includes four support legs and a connecting beam. The four support legs are rectangularly distributed and bolted to the four corners of the connecting beam. Each support leg has a height-adjustable spiral adjustment foot at its bottom. The connecting beam is an I-beam structure with a circular mounting hole in the center. The preparation reactor is fixed in the circular mounting hole by a flange.
7. The vitamin C microcapsule preparation detection and collection device according to claim 6, characterized in that, The outer wall of the reactor is provided with multiple heat dissipation fins, which are distributed at equal intervals along the axial direction of the reactor.
8. The vitamin C microcapsule preparation detection and collection device according to claim 7, characterized in that, The inner wall of the detection and acquisition body is provided with an annular guide groove, the depth of which is 2 mm to 5 mm.
9. The vitamin C microcapsule preparation detection and collection device according to claim 8, characterized in that, The upper surface of the sealing cover is provided with raised reinforcing ribs, which are distributed in a cross shape.
10. The vitamin C microcapsule preparation detection and collection device according to claim 9, characterized in that, There are 12 heat dissipation fins, which are evenly distributed along the circumference on the outer wall of the reactor.