Monosidum glutamate crystal separation device

By using a design that combines cooling pipes and heating coils with stirring blades and spiral blades in the monosodium glutamate (MSG) crystallization and separation device, the problem of crystal adhesion at high temperatures was solved, achieving uniform crystallization and efficient separation, thus improving product quality and purity.

CN223516967UActive Publication Date: 2025-11-07COFCO BIO CHEM ENERGY LONGJIANG CO LTD +1
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Patent Information

Application Number
CN202423118529.1
Authority / Receiving Office
CN · China
Patent Type
Utility models(China)
Current Assignee / Owner
Filing Date
2024-12-17
Publication Date
2025-11-07
Estimated Expiration
2034-12-17

AI Technical Summary

Technical Problem

Existing monosodium glutamate (MSG) crystallization separation devices are prone to crystal adhesion and agglomeration under high temperature conditions, which affects the accuracy and efficiency of screening and reduces product quality and purity.

Method used

Cooling pipes and heating coils are used to uniformly cool and heat the material in the crystallizer. Combined with the design of stirring blades and spiral blades, the material is ensured to be uniformly mixed and at a consistent temperature. Centrifugal force is used to separate the crystals and the mother liquor.

Benefits of technology

It improves crystallization efficiency and product quality, avoids crystal adhesion, generates uniform monosodium glutamate crystals, and enhances separation efficiency and purity.

✦ Generated by Eureka AI based on patent content.

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Abstract

The utility model belongs to the technical field of monosodium glutamate production, particularly relates to a monosodium glutamate crystal separation device, and aims to solve the problem that the quality and the purity of a product are easily affected as the conventional device is lack of cooling treatment on conveyed monosodium glutamate crystals. The surface of the feeding pipe is in threaded connection with a matched sealing cover; the crystallization tank has the beneficial effects that cooling water flows from bottom to top, and the spiral design of the cooling pipe is matched, so that materials from the bottom to the top of the crystallization tank can be relatively uniformly cooled, heat can be uniformly dissipated from the materials in the crystallization tank, the temperature reduction trend in the whole crystallization tank is relatively consistent, and the crystallization efficiency is improved. And the production of uniform monosodium glutamate crystals is facilitated, and the phenomenon that in the subsequent conveying and screening process, the crystals are easily adhered to one another to form large aggregates is avoided, so that the quality and the purity of the product are improved.
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Description

TECHNICAL FIELD

[0001] The utility model relates to a kind of fermentation equipment, specifically a monosodium glutamate crystallization separation device, belong to ethanol production technical field. BACKGROUND

[0002] Monosodium glutamate is widely used as a seasoning product, with the improvement of people's life, the output of monosodium glutamate is also greatly improved, so the method and device for producing monosodium glutamate crystal are an important daily chemical process. In the production process of monosodium glutamate, crystallization and separation are extremely critical links.

[0003] In the prior art, as disclosed in the announcement No. CN202120612350.9, a screening type monosodium glutamate crystallization separation device is provided. Then, a spiral conveying blade is arranged in the discharge pipe of the separation tank to convey the monosodium glutamate crystals discharged from the discharge port, preventing the monosodium glutamate crystals from being blocked in the discharge pipe. At the same time, the spiral conveying blade contacts with the inner wall of the discharge pipe to prevent the monosodium glutamate crystals from being left in the discharge pipe. The above-mentioned prior art scheme has the following disadvantages: the monosodium glutamate crystallization separation device cannot timely cool the conveyed monosodium glutamate crystals during use. The monosodium glutamate crystals in high-temperature state have high activity and fluidity. During conveying and screening, the crystals are easily adhered to each other, forming large agglomerates. This not only affects the accuracy and efficiency of screening, makes the filter screen easily blocked, and causes the screening process to be unable to continuously and stably proceed, but also the agglomerated crystals are uneven in size, which reduces the quality and purity of the product, and affects the subsequent packaging, storage and use effect. SUMMARY

[0004] The purpose of the utility model is to solve the problem of lack of cooling treatment for the conveyed monosodium glutamate crystals in the above-mentioned device, which easily affects the quality and purity of the product, and to provide a monosodium glutamate crystallization separation device.

[0005] The utility model realizes the above-mentioned purpose through the following technical scheme: a monosodium glutamate crystallization separation device includes a crystallization tank, a feed pipe is communicated with the top surface of the crystallization tank, a sealing cover that is suitable is connected with the surface of the feed pipe by screw thread, a separation tank is fixedly connected with the crystallization tank through a plurality of connecting supports below the crystallization tank, a discharge pipe is communicated with the bottom of the crystallization tank, one end of the discharge pipe is communicated with the top of the separation tank;

[0006] A cooling pipe is arranged on the outside of the crystallization tank, the cooling pipe is fixedly installed on the outer wall of the crystallization tank and close to the bottom position thereof, the inlet end and the outlet end of the cooling pipe are respectively located at the two ends of the cooling pipe, and the inlet end is located below the outlet end, and the cooling pipe is connected with an external cooling water source.

[0007] As a further scheme of the utility model: the inside of crystallizing tank is equipped with transmission shaft, the surface of crystallizing tank is installed with servo motor, one end of transmission shaft penetrates the top of crystallizing tank, and is fixedly connected with the output shaft coaxial line of servo motor, the surface of transmission shaft is fixedly installed with stirring blade.

[0008] As a further scheme of the utility model: the inside wall of crystallizing tank is provided with partition, heating coil is arranged in the partition, the heating coil is spirally arranged in the partition of the inside wall of crystallizing tank, and the heating coil is connected with external heat source.

[0009] As a further scheme of the utility model: the outlet end of discharge pipe is connected with separation tank in tangent direction, and the valve is installed on the discharge pipe.

[0010] As a further scheme of the utility model: the inside of separation tank is fixedly installed with filter screen in inclined mode, the lower end of filter screen is connected with discharge pipe, the end of discharge pipe extending out of separation tank is installed with discharge valve, and the bottom of separation tank is provided with discharge port.

[0011] As a further scheme of the utility model: the surface of stirring blade is integrally formed with spiral blade of spiral structure.

[0012] As a further scheme of the utility model: the inside bottom surface of separation tank is slidingly provided with push plate, the surface of one side of separation tank is fixedly installed with multistage hydraulic rod, the piston end of multistage hydraulic rod penetrates separation tank and extends into separation tank and is connected with one side of push plate.

[0013] As a further scheme of the utility model: the bottom of separation tank is fixedly installed with supporting leg, the bottom of supporting leg is provided with damping pad, and the heating coil is made of stainless steel.

[0014] As a further scheme of the utility model: the surface of feeding pipe is threadedly connected with matched sealing cover.

[0015] The utility model discloses the beneficial effect is:

[0016] 1、 the utility model discloses the cooperation of the structure such as crystallizing tank, separation tank, feeding pipe, transmission shaft, stirring blade, spiral blade, heating coil, cooling pipe, filter screen, discharge port and push plate is used, makes the stirring blade of installing on the outside of transmission shaft follow rotation, and the material in crystallizing tank is fully mixed, and the spiral blade of the surface integral molding of spiral structure of stirring blade is set, it can more quickly mix the material of newly adding with the material of having in tank, so as to guarantee the solution concentration uniformity in whole crystallizing tank, makes the crystallization process in each position can be synchronous, thereby improves crystallization efficiency;

[0017] Meanwhile, the heating coil is connected with the heat medium, the material in the crystallization tank is heated, the monosodium glutamate solution reaches the saturated state and starts to crystallize, the targeted heating mode can effectively start the crystallization process, compared with the natural cooling or slow heating mode, the time required to reach the crystallization condition is greatly shortened, so that the efficiency of the whole crystallization process is improved, the heating coil is arranged around the inner wall of the crystallization tank, the heat can be relatively uniformly distributed in the crystallization tank, so that the local overheating or supercooling condition can be avoided, the monosodium glutamate solution in the whole tank can reach the saturated state and crystallize at the appropriate temperature, which helps to generate relatively uniform monosodium glutamate crystals with regular shape, avoids uneven heating, and the crystallization of some areas is too fast, large crystal nucleus is formed, while the crystallization of other areas is too slow, finally, the size difference of the obtained crystals is large, and the product quality is affected;

[0018] 2、The utility model discloses a cooling pipe is set up to the material in the crystallization tank is cooled, and more monosodium glutamate is crystallized and separated out, and the liquid inlet end and the liquid outlet end of cooling pipe are located at both ends of cooling pipe respectively, and the liquid inlet end is located below the liquid outlet end, and the cooling pipe of spiral structure is set up, make cooling water flow from below to top, cooperate the spiral design of cooling pipe, can make the material of crystallization tank bottom to top all can get relatively uniform cooling, can make heat evenly from the material in the crystallization tank, make the temperature drop trend of whole crystallization tank be more consistent, help to generate uniform monosodium glutamate crystal, avoid the easy mutual adhesion of crystal between in the subsequent conveying and screening process, form larger agglomerate, thereby improve the quality and purity of product. ACCURACY OF DRAWINGS

[0019] Figure 1 It is the whole structure schematic view of the utility model;

[0020] Figure 2 It is the internal partial structure schematic view of the crystallization tank and the separation tank in the utility model;

[0021] Figure 3 It is the structure schematic view of the spiral blade, the discharge pipe and the cooling pipe in the utility model;

[0022] Figure 4 It is the structure schematic view of the cooling pipe in the utility model;

[0023] Figure 5 It is the structure schematic view of the heating coil in the utility model;

[0024] Figure 6 It is the structure schematic view of the push plate, the multistage hydraulic rod and the discharge port in the utility model;

[0025] Figure 7 It is the structure schematic view of the discharge pipe, the exhaust pipe and the filter screen in the utility model;

[0026] Figure 8 It is the structural schematic view of the transmission shaft, the stirring blade and the spiral blade in the utility model;

[0027] In the figure: 1, crystallization tank; 2, separation tank; 3, support leg; 4, servo motor; 5, feed pipe; 6, transmission shaft; 7, stirring blade; 8, spiral blade; 9, partition; 10, heating coil; 11, cooling pipe; 12, liquid inlet; 13, liquid outlet; 14, valve; 15, filter screen; 16, discharge pipe; 17, discharge port; 18, discharge valve; 19, multi-stage hydraulic rod; 20, push plate; 21, discharge pipe. DETAILED DESCRIPTION

[0028] The technical solutions in the embodiments of the utility model will be clearly and completely described below with reference to the drawings in the embodiments of the utility model. Obviously, the described embodiments are only part of the embodiments of the utility model, not all the embodiments. Based on the embodiments in the utility model, all other embodiments obtained by those skilled in the art without creative labor fall within the scope of protection of the utility model.

[0029] Embodiment one

[0030] As shown in Figures 1 to 8 A monosodium glutamate crystallization and separation device, which comprises a crystallization tank 1, a feed pipe 5 is communicated with the top surface of the crystallization tank 1, a sealing cover matched with the feed pipe 5 is threadedly connected to the surface of the feed pipe 5, a separation tank 2 is fixedly connected to the lower side of the crystallization tank 1 through a plurality of connecting supports, a discharge pipe 21 is communicated with the bottom of the crystallization tank 1, and one end of the discharge pipe 21 is communicated with the top of the separation tank 2.

[0031] A cooling pipe 11 is arranged on the outer side of the crystallization tank 1, the cooling pipe 11 is fixedly installed on the outer wall of the crystallization tank 1 and close to the bottom position, the liquid inlet 12 and the liquid outlet 13 of the cooling pipe 11 are respectively located at the two ends of the cooling pipe 11, the liquid inlet 12 is located below the liquid outlet 13, and the cooling pipe 11 is connected with an external cooling water source.

[0032] When the crystallization process reaches a certain extent, the heat source of the heating coil 10 is turned off, and the cooling water source of the cooling pipe 11 is turned on to cool the material in the crystallization tank 1, so that more monosodium glutamate crystals are precipitated. The liquid inlet end 12 and the liquid outlet end 13 of the cooling pipe 11 are located at both ends of the cooling pipe 11, and the liquid inlet end 12 is located below the liquid outlet end 13. The spiral structure of the cooling pipe 11 is arranged so that the cooling water flows from bottom to top. The spiral design of the cooling pipe 11 can make the material from the bottom to the top of the crystallization tank 1 be relatively uniformly cooled, and the heat can be uniformly dissipated from the material in the crystallization tank 1, so that the temperature in the entire crystallization tank 1 decreases uniformly, which helps to form uniform monosodium glutamate crystals and avoids the crystals being easily adhered to each other during subsequent transportation and screening, thereby improving the quality and purity of the product.

[0033] Further, the inside of the crystallization tank 1 is provided with a transmission shaft 6, and the surface of the crystallization tank 1 is provided with a servo motor 4. One end of the transmission shaft 6 penetrates the top of the crystallization tank 1 and is fixedly connected with the output shaft of the servo motor 4 in coaxial line. The surface of the transmission shaft 6 is fixedly provided with stirring blades 7.

[0034] The servo motor 4 is turned on, which can drive the transmission shaft 6 installed at the output shaft end of the servo motor 4 to rotate, and then the stirring blades 7 installed on the outside of the transmission shaft 6 can rotate to fully mix the material in the crystallization tank 1.

[0035] Example Two

[0036] Based on the improvement of Example One:

[0037] Further, a partition 9 is arranged on the inner wall of the crystallization tank 1, and a heating coil 10 is arranged in the partition 9. The heating coil 10 is spirally arranged in the partition 9 of the inner wall of the crystallization tank 1, and the heating coil 10 is connected with an external heat source.

[0038] The heating coil 10 is connected with a heat medium to heat the material in the crystallization tank 1, so that the monosodium glutamate solution reaches a saturated state and starts to crystallize. This targeted heating method can effectively start the crystallization process, greatly shorten the time required to reach the crystallization condition compared with natural cooling or slow heating, thereby improving the efficiency of the entire crystallization process. The heating coil 10 is arranged around the inner wall of the crystallization tank 1, which can make the heat be relatively uniformly distributed in the crystallization tank 1. This can avoid local overheating or overcooling, and ensure that the monosodium glutamate solution in the entire tank can reach a saturated state at a suitable temperature and crystallize, which helps to form monosodium glutamate crystals with relatively uniform size and regular shape, and avoids uneven heating, which may cause some areas to crystallize too quickly and form larger crystal nuclei, while other areas crystallize too slowly, resulting in a large difference in crystal size and affecting product quality.

[0039] Further, the outlet end of the discharge pipe 21 is connected to the separation tank 2 in a tangential direction, and a valve 14 is installed on the discharge pipe 21.

[0040] When the mixture of monosodium glutamate crystals and mother liquor enters the separation tank 2 from the tangential direction through the discharge pipe 21, a rotating motion is generated in the separation tank 2, which causes the mixture to generate a centrifugal force. Under the action of the centrifugal force, the heavier monosodium glutamate crystals are thrown to the edge and bottom of the separation tank 2, and the lighter mother liquor is concentrated in the central area or near the top. This distribution helps to preliminarily separate the crystals and the mother liquor, reduces the burden of subsequent separation devices such as the filter screen 15, and improves the overall separation efficiency.

[0041] Further, the filter screen 15 is fixedly installed inside the separation tank 2 at an inclination, the lower end of the filter screen 15 is connected to a discharge pipe 16, the end of the discharge pipe 16 extending out of the separation tank 2 is provided with a discharge valve 18, and the bottom of the separation tank 2 is provided with a discharge port 17.

[0042] Opening the valve 14 on the discharge pipe 21 causes the crystals to enter the separation tank 2 through the discharge pipe 21. In the separation tank 2, the monosodium glutamate crystals are screened on the filter screen 15. The smaller particles pass through the filter screen 15 and fall to the inner bottom of the separation tank 2, and the larger particles are intercepted on the surface of the filter screen 15 and are discharged through the discharge pipe 16, and then are re-injected into the crystallization tank 1 and can be used as crystal seeds to drive the crystallization of the material in the tank.

[0043] Further, the surface of the stirring blade 7 is integrally formed with a helical blade 8 having a helical structure.

[0044] The helical blade 8 integrally formed with the surface of the stirring blade 7 having a helical structure can more quickly mix the newly added material with the existing material in the tank, so as to ensure that the solution concentration in the entire crystallization tank 1 is uniform, and the crystallization process can be synchronized at each position, thereby improving the crystallization efficiency.

[0045] Further, a push plate 20 is slidingly attached to the inner bottom surface of the separation tank 2, a multi-stage hydraulic rod 19 is fixedly installed on one side surface of the separation tank 2, and the piston end of the multi-stage hydraulic rod 19 penetrates through the separation tank 2 and extends into the separation tank 2, and is connected to one side of the push plate 20.

[0046] The relatively pure monosodium glutamate crystals falling to the inner bottom of the separation tank 2 are pushed out of the discharge port 17 by the push plate 20 driven by the multi-stage hydraulic rod 19, and are concentrated and collected for processing.

[0047] Further, support legs 3 are fixedly installed at the bottom of the separation tank 2, and the bottom of the support legs 3 is provided with shock-absorbing pads. The heating coil 10 is made of stainless steel.

[0048] The bottom of the separation tank 2 is provided with support legs 3, and the bottom of the support legs 3 is provided with shock-absorbing pads to reduce vibration during operation of the equipment.

[0049] The surface of the feed pipe 5 is threadedly connected with a matching sealing cover.

[0050] The sealing cover is opened when the material is added, and after the material is added, the sealing cover is tightened at the end of the feed pipe 5 to prevent impurities from entering.

[0051] Working principle: in use, first open the sealing cover threadedly connected to the surface of the feed pipe 5, then pour the raw material into the crystallization tank 1 through the feed pipe 5, start the servo motor 4, then the servo motor 4 can drive the transmission shaft 6 installed at the output shaft end to rotate, then the stirring blade 7 installed on the outside of the transmission shaft 6 can rotate, fully mix the material in the crystallization tank 1, and the spiral blade 8 integrally formed on the surface of the stirring blade 7 has a spiral structure, which can more quickly mix the newly added material with the existing material in the tank to ensure uniform solution concentration in the entire crystallization tank 1, so that the crystallization process can be synchronized at all positions, thereby improving the crystallization efficiency;

[0052] At the same time, the heating coil 10 is connected to a heating medium to heat the material in the crystallization tank 1, so that the monosodium glutamate solution reaches a saturated state and begins to crystallize. This targeted heating method can effectively start the crystallization process, compared with natural cooling or slow heating, greatly shortening the time required to reach the crystallization condition, thereby improving the efficiency of the entire crystallization process. The heating coil 10 is arranged around the inner wall of the crystallization tank 1, which can relatively evenly distribute the heat in the crystallization tank 1, so as to avoid local overheating or undercooling, and ensure that the monosodium glutamate solution reaches a saturated state and crystallizes at a suitable temperature throughout the tank body. This helps to generate relatively uniform and regular-shaped monosodium glutamate crystals, avoids uneven heating, which may cause some areas to crystallize too quickly, forming larger crystal nuclei, while other areas crystallize too slowly, resulting in a large difference in crystal size and affecting product quality.

[0053] When the crystallization process reaches a certain extent, the heat source of the heating coil 10 is turned off, and the cooling water source of the cooling pipe 11 is turned on to cool the material in the crystallization tank 1, so that more monosodium glutamate crystals are precipitated. The liquid inlet end 12 and the liquid outlet end 13 of the cooling pipe 11 are located at both ends of the cooling pipe 11, and the liquid inlet end 12 is located below the liquid outlet end 13. The spiral structure of the cooling pipe 11 allows the cooling water to flow from bottom to top. The spiral design of the cooling pipe 11 can uniformly cool the material from the bottom to the top of the crystallization tank 1, and the heat can be evenly dissipated from the material in the crystallization tank 1, so that the temperature in the entire crystallization tank 1 decreases uniformly, which helps to form uniform monosodium glutamate crystals and avoid the mutual adhesion of the crystals during subsequent transportation and screening, thereby improving the quality and purity of the product.

[0054] After the crystallization is completed, the valve 14 on the discharge pipe 21 is opened, and the crystals are pushed into the separation tank 2 through the discharge pipe 21. In the separation tank 2, the monosodium glutamate crystals are screened on the filter screen 15. The smaller particles pass through the filter screen 15 and fall to the inner bottom of the separation tank 2, and the relatively pure monosodium glutamate crystals falling to the inner bottom of the separation tank 2 are pushed out of the discharge port 17 by the push plate 20 driven by the multi-stage hydraulic rod 19, and are collected and processed. The larger particles are intercepted on the surface of the filter screen 15 and are discharged through the discharge pipe 16, and are again put into the crystallization tank 1 and can be used as crystal seeds to drive the crystallization of the material in the tank.

[0055] When the mixture containing monosodium glutamate crystals and mother liquor enters the separation tank 2 from the tangent direction through the discharge pipe 21, a rotating motion is generated in the separation tank 2. This rotating motion causes the mixture to generate a centrifugal force. Under the action of the centrifugal force, the heavier monosodium glutamate crystals are thrown to the edge and bottom of the separation tank 2, and the lighter mother liquor is concentrated in the central area or near the top. This distribution helps to preliminarily separate the crystals and the mother liquor, reduces the burden of the subsequent separation devices such as the filter screen 15, and improves the overall separation efficiency.

[0056] It should be noted that the discharge valve 18 is used to control the opening and closing of the discharge pipe 16.

[0057] It should be noted that the bottom of the separation tank 2 is provided with support legs 3, and the bottom of the support legs 3 is provided with shock-absorbing pads to reduce vibration during equipment operation.

[0058] It is apparent for a person skilled in the art that the present application is not limited to the details of the above-described exemplary embodiments, but that it can be implemented in other concrete forms without departing from the spirit or the essential characteristics of the present application. Therefore, the embodiments should be considered as exemplary and non-limiting, the scope of the present application being defined by the claims appended hereto rather than by the above description, and all the changes which fall within the meaning and the scope of the equivalent elements of the claims are intended to be embraced therein. Any reference signs in the claims should not be construed as limiting the claims to the figures in which the reference signs are used.

[0059] Furthermore, it should be understood that although the present specification describes exemplary embodiments, not every embodiment contains only one independent technical solution, and the present specification is described in this way only for the sake of clarity, and a person skilled in the art should consider the specification as a whole, and the technical solutions in each embodiment can also be appropriately combined to form other embodiments that a person skilled in the art can understand.

Claims

1. A monosodium glutamate crystallization separation apparatus comprising a crystallization tank (1), characterized in that: The top surface of the crystallization tank (1) is communicated with a feeding pipe (5), a plurality of connecting supports are fixedly connected below the crystallization tank (1) and a separation tank (2), the bottom of the crystallization tank (1) is communicated with a discharging pipe (21), one end of the discharging pipe (21) is communicated with the top of the separation tank (2); The outer side of the crystallization tank (1) is provided with a cooling pipe (11), the cooling pipe (11) is spirally fixedly installed on the outer wall of the crystallization tank (1) and close to the bottom position, the liquid inlet end (12) and the liquid outlet end (13) of the cooling pipe (11) are located at the two ends of the cooling pipe (11) respectively, and the liquid inlet end (12) is located below the liquid outlet end (13), and the cooling pipe (11) is connected with an external cooling water source.

2. The monosodium glutamate crystallization separation device according to claim 1, characterized in that: The inside of the crystallization tank (1) is provided with a transmission shaft (6), the surface of the crystallization tank (1) is provided with a servo motor (4), one end of the transmission shaft (6) penetrates through the top of the crystallization tank (1) and is fixedly connected with the output shaft of the servo motor (4) in the same axis line, and the surface of the transmission shaft (6) is fixedly installed with stirring blades (7).

3. The monosodium glutamate crystallization separation device according to claim 1, characterized in that: The inner wall of the crystallization tank (1) is provided with a partition layer (9), the partition layer (9) is provided with a heating coil (10), the heating coil (10) is spirally wound in the partition layer (9) of the inner wall of the crystallization tank (1), and the heating coil (10) is connected with an external heat source.

4. The monosodium glutamate crystallization separation device according to claim 1, characterized in that: The outlet end of the discharging pipe (21) is communicated with the separation tank (2) in the tangential direction of the separation tank (2), and the discharging pipe (21) is provided with a valve (14).

5. The monosodium glutamate crystallization separation device according to claim 1, characterized in that: The inside of the separation tank (2) is fixedly installed with a filter screen (15) in an inclined manner, the lower end of the filter screen (15) is connected with a discharge pipe (16), one end of the discharge pipe (16) extending out of the separation tank (2) is provided with a discharge valve (18), and the bottom of the separation tank (2) is provided with a discharge port (17).

6. The monosodium glutamate crystallization separation device according to claim 2, characterized in that: The surface of the stirring blade (7) is integrally formed with a helical blade (8) of a spiral structure.

7. The monosodium glutamate crystallization separation device according to claim 1, characterized in that: The inside bottom surface of the separation tank (2) is slidingly provided with a push plate (20), one side surface of the separation tank (2) is fixedly installed with a multi-stage hydraulic rod (19), the piston end of the multi-stage hydraulic rod (19) penetrates through the separation tank (2) and extends into the separation tank (2) and is connected with one side of the push plate (20).

8. The monosodium glutamate crystallization separation device according to claim 3, characterized in that: The bottom of the separation tank (2) is fixedly installed with a supporting leg (3), the bottom of the supporting leg (3) is provided with a shock pad, and the heating coil (10) is made of stainless steel.

9. The monosodium glutamate crystallization separation apparatus according to claim 1, characterized by: The surface of the feeding pipe (5) is threadedly connected with a sealing cover matched therewith.

Citation Information

Patent Citations

  • Screening type monosodium glutamate crystal separation equipment

    CN214440660U