CN110656206A - Novel sucrose refining method capable of controlling granularity - Google Patents

Novel sucrose refining method capable of controlling granularity Download PDF

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CN110656206A
CN110656206A CN201910906021.2A CN201910906021A CN110656206A CN 110656206 A CN110656206 A CN 110656206A CN 201910906021 A CN201910906021 A CN 201910906021A CN 110656206 A CN110656206 A CN 110656206A
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sucrose
crystal
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crystallization
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CN110656206B (en
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唐波
彭立辉
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Hunan Green Party Pharmaceutical Co Ltd
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    • C13SUGAR INDUSTRY
    • C13BPRODUCTION OF SUCROSE; APPARATUS SPECIALLY ADAPTED THEREFOR
    • C13B20/00Purification of sugar juices
    • C13B20/12Purification of sugar juices using adsorption agents, e.g. active carbon
    • C13B20/123Inorganic agents, e.g. active carbon
    • CCHEMISTRY; METALLURGY
    • C13SUGAR INDUSTRY
    • C13BPRODUCTION OF SUCROSE; APPARATUS SPECIALLY ADAPTED THEREFOR
    • C13B20/00Purification of sugar juices
    • C13B20/16Purification of sugar juices by physical means, e.g. osmosis or filtration
    • CCHEMISTRY; METALLURGY
    • C13SUGAR INDUSTRY
    • C13BPRODUCTION OF SUCROSE; APPARATUS SPECIALLY ADAPTED THEREFOR
    • C13B30/00Crystallisation; Crystallising apparatus; Separating crystals from mother liquors ; Evaporating or boiling sugar juice
    • C13B30/02Crystallisation; Crystallising apparatus

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Abstract

The invention discloses a novel sucrose refining method capable of controlling granularity, which comprises the steps of dissolving and decoloring edible sucrose to obtain refined filtrate, concentrating and crystallizing the refined filtrate to obtain sucrose crystals, purifying and drying the sucrose crystals to obtain medicinal sucrose crystal grains. The crystallization method combining seed crystal crystallization and ultrasonic wave stimulation assisted crystallization is creatively adopted, the grain size of the medicinal sucrose crystal is effectively controlled by accurately controlling the parameters of seed crystal adding time, seed crystal adding amount, ultrasonic frequency, ultrasonic wave stimulation crystallization time, stirring speed and the like, the sucrose crystallization yield is improved, and the characteristics of small grain size, good fluidity and good solubility of the medicinal sucrose crystal are realized, so that the performance requirements of a direct-compression solid preparation on the medicinal sucrose auxiliary material are met.

Description

Novel sucrose refining method capable of controlling granularity
Technical Field
The invention relates to the technical field of sucrose refining, in particular to a novel sucrose refining method capable of controlling particle size.
Background
Sucrose has been used as a pharmaceutic adjuvant at home and abroad for hundreds of years, and has been used as food for a longer time. It can be used as excipient, correctant, coating agent, granulating agent, suspension, sweetener, filler, therapeutic agent, and tackifier. 85% syrup or aromatic syrup is used as correctant for oral liquid preparation, 50% -67% syrup is used as binder for wet granulation, sucrose powder can be used as dry binder, sucrose can be used as binder for dry tabletting, and can be used as filler and sweetener for chewable tablet and lozenge. Therefore, pharmaceutical sucrose is widely used in the production of solid preparations, is used in large amounts as an important filler and taste-improving agent, and when the tablet formulation contains a large amount of sugar, the hardness of the tablet can be increased but the degree of disintegration is deteriorated.
Medicinal grade sucrose belongs to adjuvant drugs, and sucrose cannot simultaneously have low bulk density, good fluidity, mixing property and excellent compressibility even being subjected to sufficient pulverization treatment due to its natural crystal structure. On one hand, common sucrose is in a natural crystallization mode, crystal particles are large in particle size, and although the flowability is good, the original particles exist in the tablet by direct tabletting, so that the appearance, dissolution, disintegration and other properties of the tablet are influenced; on the other hand, after sucrose is crushed into powdered sugar, although the solubility is improved, the crystal form of the product is damaged, the powdered sugar is easy to agglomerate, the flowability of the powdered sugar is poor, the uniform mixing is poor, the feeding cannot be smooth in the production of tablets, and the uniform tablets cannot be pressed. Therefore, even if the existing medicinal sucrose is widely applied, the existing medicinal sucrose can only be applied to the conventional non-direct-compression solid preparation production process in a sucrose tablet, cannot be applied to the direct-compression solid preparation process, and cannot ensure that the tablet has good dissolution and disintegration properties. There is a need to be able to prepare a pharmaceutical sucrose adjuvant with low bulk density, good flowability, uniformity and good compressibility.
Disclosure of Invention
The invention aims to solve the technical problems that the crystal form of sucrose powder prepared by the prior art is damaged and easy to agglomerate, the flowability of the powder is poor, and the uniform mixing is poor, and provides a novel sucrose refining method which has mild purification process conditions, is simple and feasible, has lower cost, and is environment-friendly and capable of controlling the granularity.
The purpose of the invention is realized by the following technical scheme:
a novel sucrose refining method with controllable particle size comprises the following steps:
s1, dissolving and decoloring: dissolving edible sucrose in deionized water, adding decolorizing agent, stirring at constant temperature, and filtering to remove solid impurities to obtain fine filtrate.
S2, concentrating and crystallizing, namely stirring the fine filtrate obtained in the step S1, concentrating until the sugar brix is 87 ~ 92 degrees Bx, adding a certain amount of sucrose crystal seeds, stirring and dispersing, and starting ultrasonic wave to stimulate and crystallize to obtain a crystalline liquid.
S3, separation and purification: and (4) separating the crystal liquid obtained in the step (S2) into coarse crystal grains and mother liquid, adding purified water into the coarse crystal grains, stirring, and performing centrifugal separation to obtain crystal washing grains and crystal washing liquid.
S4, drying and screening: and drying and screening the crystal washing crystal grains obtained in the step S3 to obtain medicinal sucrose crystal grains.
Further, the edible sucrose dissolved in the deionized water in S1 is stirred at a constant temperature of 75 ~ 85 ℃ and the mass ratio of the edible sucrose to the deionized water is 2 ~ 3: 1.
The S1 decolorant is added in an amount of 0.05 ~ 0.1.1% of the edible sucrose, adsorbs and removes pigments contained in the edible sucrose, preferably, the S1 decolorant is injection-grade medicinal activated carbon, and can adsorb and remove tiny particle impurities contained in the edible sucrose at the same time.
Further, the fine filtration liquid of S2 is concentrated under reduced pressure at 70 ~ 80 deg.C under-0.09 ~ -0.07 Mpa.
Solution crystallization is the process by which a substance is transformed from a liquid state to a crystalline state, which involves two phases, nucleation and crystal growth. The aim of seeking high crystal growth rate in an industrial crystallizer is to improve the production capacity of equipment, but the crystallization is rapid, the crystal nucleus quantity is difficult to control, the crystal nucleus production speed is not matched with the crystal nucleus growth speed, so that the size of the recrystallized crystals cannot be controlled, granular crystals with different sizes are easy to appear in the production process, the yield and the quality of finished products are influenced, and the requirement that sucrose powder is used as a solid preparation cannot be met by adopting a recrystallization mode for providing supersaturation to improve the growth rate of the crystals. Through scientific analysis and a large number of experiments, the method realizes the control of the grain size of the sucrose crystal by adopting ultrasonic waves and the stimulation crystallization added by the seed crystal and controlling the time for adding the seed crystal, the quality of the seed crystal, the frequency of the ultrasonic waves and the time for stimulating the crystallization by the ultrasonic waves.
Furthermore, experiments prove that the method provided by the invention has a better crystal growth speed for adding the seed crystal when the brix of the sucrose concentrated solution is 87 ~ 92 Bx, does not cause the grain size of the prepared crystal to be too large or too small, can improve the sucrose crystal yield and reduce the sucrose crystallization time, and meanwhile, the addition amount of the sucrose seed crystal in S2 is 0.1 ~ 0.3.3% of the quality of edible sucrose, the quantity of the seed crystal influences the generation of the crystal nucleus and the quality and yield of the crystal nucleus.
Furthermore, the frequency of ultrasonic wave stimulated crystallization of S2 is 1500 ~ Hz, the time of ultrasonic wave stimulated crystallization is 10 ~ min, in the process of crystal growth, ultrasonic wave is assisted, additional sound wave generates cavitation bubbles, the cavitation bubbles expand and grow, collapse quickly, when the bubbles collapse, a fast moving liquid flow is generated, and the liquid flow generates great impact force.
Further, the stirring speed of S2 is 22 ~ 35r/min, and preferably, the stirring speed of S2 is 28 r/min.
Furthermore, the highest speed of centrifugation is 1000 ~ 1200r/min, and the concentrated solution on the surface of the crystal is washed to prevent the crystal grains from caking and ensure better fluidity of powdered sugar.
Furthermore, the drying temperature of the crystal grain of the crystal washing of S4 is 63 ~ 67 ℃, the drying time is 60 ~ 150min, the grain diameter of the obtained sucrose crystal grain prepared by the method is 20 ~ 80 meshes, the purity reaches 99.9 ~ 99.99.99%, the fluidity is good, the moisture content is below 1.0%, and the product yield reaches 60 ~ 67%.
Compared with the prior art, the beneficial effects are:
the invention creatively adopts edible sucrose as a raw material to produce and prepare medicinal refined sucrose, scientifically designs purification steps, adopts dissolution and decoloration, reduced pressure concentration, seed crystal crystallization and ultrasonic stimulation crystallization, and separates and dries, and can obtain the sucrose auxiliary material which accords with Chinese pharmacopoeia by crystallization at a high speed under the condition of not using other organic solvents.
In the process of refining sucrose, the invention realizes effective control of the particle size of sucrose crystals by accurately controlling the parameters of the seed crystal addition time, the seed crystal addition amount, the ultrasonic frequency, the ultrasonic wave stimulated crystallization time, the stirring speed and the like, and simultaneously improves the sucrose crystallization yield, so that the prepared medicinal sucrose crystals have the characteristics of small particle size, good fluidity and good solubility, thereby meeting the performance requirements of a direct-compression solid preparation on medicinal sucrose auxiliary materials.
The method adopts the crystal seed crystallization and ultrasonic stimulation assisted crystallization modes, the grain diameter of the prepared sucrose crystal is 20 ~ 80 meshes (the optimal grain diameter range used by the solid preparation), the purity reaches 99 percent, and the yield is not lower than 60 percent.
Drawings
FIG. 1 is a flow chart of the preparation of the present invention;
FIG. 2 is a diagram of a production apparatus for refining sucrose with controllable particle size according to the present invention.
The device comprises a dissolving tank 1, a stirrer 2, a steam jacket 3, a filter screen 4, a titanium rod filter 5, a fine filter liquid tank 6, a concentration tank 7, a purified water inlet 8, a vacuum generator 9, an ultrasonic generator 10, a crystal seed dispenser 11, a centrifuge 12 and a fluidization vibrator 13.
Detailed Description
The following examples are further explained and illustrated, but the present invention is not limited in any way by the specific examples. Unless otherwise indicated, the methods and equipment used in the examples are conventional in the art and all materials used are conventional commercially available materials.
The required production equipment is provided by the following companies:
device name Model number Number of Production plant
Dissolving tank 5m3 1 Zibo bin combined chemical and equipment Limited
Titanium rod filter 9 core 30 inches 1 Hening hengtai filtration plant
Fine filtering liquid tank 22m3 1 Ningxiang county culture of industry and trade Limited
Concentrating and crystallizing tank 3m3 1 Zibo bin combined chemical and equipment Limited
Clean centrifugal machine PSB800-100L 1 Zhang Jia City Chengjia machinery Co Ltd
Fluidized vibration bed dryer ZGL-4.5×0.6 1 Changzhou new industry granulation drying equipment Co
Vibrating screen S4910-B 1 Xinxiangdongzi mechanical manufacturing Co Ltd
Example 1
This embodiment provides a production facility that cane sugar of novel controllable granularity is refined.
A novel sucrose refining production system with controllable granularity comprises a dissolving tank 1, a titanium rod filter 5, a fine filtration liquid tank 6, a concentration tank 7, a centrifuge 12 and a fluidization vibrator 13. The discharge port of the dissolving tank 1 is connected with the feed port of the titanium rod filter 5, the discharge port of the titanium rod filter 5 is connected with the feed port of the fine filtration liquid tank 6, the discharge port of the fine filtration liquid tank 6 is connected with the feed port of the concentration tank 7, the discharge port of the concentration tank 7 is connected with the centrifuge 12, and the centrifuge 12 is connected with the inlet of the fluidization vibration machine 13.
The upper part of the dissolving tank 1 is provided with a feed inlet, the inside of the dissolving tank is provided with a stirrer 2, and a steam jacket 3 is arranged around the dissolving tank 1 and used for heating and dissolving edible sucrose. A layer of filter screen 4 is arranged at the discharge port of the dissolving tank 1 and is used for preliminary filtering of the sucrose dissolving solution.
A stirrer 7 is arranged in the fine filtration liquid tank 6, and a filter screen 4 is arranged at a discharge port of the fine filtration liquid tank 6. The upper part of the concentration tank 7 is provided with a purified water inlet 8, a seed crystal dispenser 11 and a vacuum generator 9, the inside of the concentration tank is provided with a stirrer 2 and an ultrasonic generator 10, and the periphery of the outside of the concentration tank is provided with a steam jacket 3.
The titanium rod filter 5 is not more than 0.5 micron, the sieve plate of the fluidization vibration machine 13 is in a fish scale hole shape, the aperture is 20 ~ 80 meshes, and the problem of hole leakage caused by small product fineness is avoided.
Example 2
This example provides a novel sucrose refining method with controllable particle size, which comprises the following steps:
s1, dissolving and decoloring: dissolving 10kg of edible sucrose in 4kg of deionized water, adding 8g of activated carbon for decolorization, stirring at a constant temperature of 80 ℃ until the sucrose is dissolved, and filtering to obtain a sucrose fine filtrate.
S2, concentrating and crystallizing, namely stirring the fine sucrose filtrate obtained from the step S1 at 28r/min, reducing the pressure to-0.09 ~ -0.07Mpa, concentrating at 70 ~ 80 ℃ until the sugar brix is 90 degrees Bx, adding 20g of seed crystal, starting ultrasonic waves, and stimulating and crystallizing for 25min by regulating the frequency to 1620Hz to obtain a crystalline liquid.
S3, separation and purification, namely centrifugally separating the crystal liquid obtained in the step S2 into coarse crystal grains and mother liquid at 1000 ~ 1200r/min, adding purified water into the coarse crystal grains, stirring, and centrifugally separating to obtain crystal washing grains and crystal washing liquid.
S4, drying and screening, namely drying crystal grains obtained in the step S3 at 63 ~ 67 ℃ to obtain medicinal sucrose crystal grains.
Example 3
This example provides a novel sucrose refining method with controllable particle size, which comprises the following steps:
s1, dissolving and decoloring: dissolving 10kg of edible sucrose in 5kg of deionized water, adding 10g of activated carbon for decolorization, stirring at a constant temperature of 85 ℃ until the sucrose is dissolved, and filtering to obtain a sucrose fine filtrate.
S2, concentrating and crystallizing, namely stirring the refined sucrose filtrate obtained in the step S1 at 35r/min, reducing the pressure to-0.09 ~ -0.07Mpa, concentrating at 70 ~ 80 ℃ until the sugar brix is 87 ℃ Bx, adding 30g of seed crystal, starting ultrasonic waves, and stimulating and crystallizing at the frequency of 1700Hz for 20min to obtain a crystalline liquid.
S3, separation and purification, namely centrifugally separating the crystal liquid obtained in the step S2 into coarse crystal grains and mother liquid at 1000 ~ 1200r/min, adding purified water into the coarse crystal grains, stirring, and centrifugally separating to obtain crystal washing grains and crystal washing liquid.
S4, drying and screening, namely drying the crystal washing crystal grains obtained in the step S3 at 63 ~ 67 ℃ to obtain medicinal sucrose crystal grains in the embodiment 4
This example provides a novel sucrose refining method with controllable particle size, which comprises the following steps:
s1, dissolving and decoloring: dissolving 10kg edible sucrose in 3.3kg deionized water, adding 5g active carbon for decolorization, stirring at 75 deg.C until sucrose is dissolved, and filtering to obtain sucrose fine filtrate.
S2, concentrating and crystallizing, namely stirring the fine sucrose filtrate obtained from the step S1 at 22r/min, reducing the pressure to-0.09 ~ -0.07Mpa, concentrating at 70 ~ 80 ℃ until the sugar brix is 92 ℃ Bx, adding 10g of seed crystal, starting ultrasonic waves, and stimulating and crystallizing at 1500Hz for 20min to obtain a crystalline liquid.
S3, separation and purification, namely centrifugally separating the crystal liquid obtained in the step S2 into coarse crystal grains and mother liquid at 1000 ~ 1200r/min, adding purified water into the coarse crystal grains, stirring, and centrifugally separating to obtain crystal washing grains and crystal washing liquid.
S4, drying and screening, namely drying the crystal washing crystal grains obtained in the step S3 at 63 ~ 67 ℃ to obtain medicinal sucrose crystal grains in the embodiment 5
This example provides a novel sucrose refining method with controllable particle size, which comprises the following steps:
s1, dissolving and decoloring: dissolving 10kg of edible sucrose in 4kg of deionized water, adding 8g of activated carbon for decolorization, stirring at a constant temperature of 80 ℃ until the sucrose is dissolved, and filtering to obtain a sucrose fine filtrate.
S2, concentrating and crystallizing, namely stirring the fine sucrose filtrate obtained from the step S1 at 28r/min, reducing the pressure to-0.09 ~ -0.07Mpa, concentrating at 70 ~ 80 ℃ until the sugar brix is 87 DEG Bx, adding 10g of seed crystal, starting ultrasonic waves, and stimulating and crystallizing at the frequency of 1700Hz for 20min to obtain a crystalline liquid.
S3, separation and purification, namely centrifugally separating the crystal liquid obtained in the step S2 into coarse crystal grains and mother liquid at 1000 ~ 1200r/min, adding purified water into the coarse crystal grains, stirring, and centrifugally separating to obtain crystal washing grains and crystal washing liquid.
S4, drying and screening, namely drying crystal grains obtained in the step S3 at 63 ~ 67 ℃ to obtain medicinal sucrose crystal grains.
Example 6
This example provides a novel sucrose refining method with controllable particle size, which comprises the following steps:
s1, dissolving and decoloring: dissolving 10kg of edible sucrose in 4kg of deionized water, adding 8g of activated carbon for decolorization, stirring at a constant temperature of 80 ℃ until the sucrose is dissolved, and filtering to obtain a sucrose fine filtrate.
S2, concentrating and crystallizing, namely stirring the fine sucrose filtrate obtained from the step S1 at 28r/min, reducing the pressure to-0.09 ~ -0.07Mpa, concentrating at 70 ~ 80 ℃ until the sugar brix is 92 degrees Bx, adding 30g of seed crystal, starting ultrasonic waves, and stimulating and crystallizing for 30min by regulating the frequency to 1500Hz to obtain a crystalline liquid.
S3, separation and purification, namely centrifugally separating the crystal liquid obtained in the step S2 into coarse crystal grains and mother liquid at 1000 ~ 1200r/min, adding purified water into the coarse crystal grains, stirring, and centrifugally separating to obtain crystal washing grains and crystal washing liquid.
S4, drying and screening, namely drying crystal grains obtained in the step S3 at 63 ~ 67 ℃ to obtain medicinal sucrose crystal grains.
Comparative example 1
The comparative example adopts a sucrose supersaturation cooling recrystallization method, i.e. excessive sucrose is dissolved at 90 ℃, activated carbon is added for decolorization, then filtration is carried out to obtain a sucrose saturated solution, stirring is carried out at 35r/min, pressure is reduced to-0.09 ~ -0.07Mpa, then cooling is carried out to normal temperature at the cooling rate of 10 ℃/h, filtration and drying are carried out, and sucrose crystals are obtained.
Comparative example 2
This comparative example is the same process as example 2 except that it concentrates the sucrose fine filtrate to a brix of 80 Bx.
Comparative example 3
This comparative example is the same as example 2 except that it did not use ultrasonic stimulation to crystallize.
Comparative example 4
This comparative example is the same as example 2 except that no seed crystal was added.
Comparative example 5
This example prepared pharmaceutical sucrose according to the method described in the patent No. CN201510608123.8 for the production of pharmaceutical sucrose.
Examples of the experiments
According to the quality standard of sucrose pharmaceutic adjuvants in the Chinese pharmacopoeia, the particle size distribution, the product yield, the finished product purity and the impurity types of the sucrose prepared in the examples and the comparative examples are detected and compared, the detection method refers to the Chinese pharmacopoeia, and the results are shown in the table 1:
TABLE 1
Figure DEST_PATH_IMAGE001
The pharmaceutical grade sucrose crystals prepared in example 2 were examined for the performance of sucrose according to the fourth part of the "chinese pharmacopoeia" 2015 edition, and the results are shown in table 2:
TABLE 2
Figure DEST_PATH_IMAGE002
In order to further verify the feasibility of the production process of the method, a pilot scale experiment is carried out on the novel sucrose refining method with controllable granularity, and the production process is as follows:
s1, dissolving and decoloring: dissolving 500kg of edible sucrose in 200kg of deionized water, adding 400g of activated carbon for decolorization, stirring at a constant temperature of 80 ℃ until the sucrose is dissolved, and filtering to obtain a sucrose fine filtrate.
S2, concentrating and crystallizing, namely stirring the fine sucrose filtrate obtained from the step S1 at 28r/min, reducing the pressure to-0.09 ~ -0.07Mpa, concentrating at 70 ~ 80 ℃ until the sugar brix is 90 degrees Bx, adding 1kg of seed crystal, starting ultrasonic waves, and stimulating and crystallizing for 25min by regulating the frequency to 1620Hz to obtain a crystalline liquid.
S3, separation and purification: centrifugally separating the crystal liquid obtained in the step S2 into coarse crystal grains and mother liquid, adding purified water into the coarse crystal grains, stirring, and centrifugally separating to obtain crystal washing grains and crystal washing liquid;
s4, drying and screening, namely drying crystal grains obtained in the step S3 at 63 ~ 67 ℃ to obtain medicinal sucrose crystal grains.
3 pilot experiments are carried out according to the method, the medicinal sucrose crystals obtained from the pilot experiments are detected according to Chinese pharmacopoeia for particle size distribution, product yield, finished product purity and impurity types, and the results are shown in Table 3:
the method for preparing the sucrose crystal has the advantages that the particle size of the sucrose crystal is 20 ~ 80 meshes (the optimal particle size range used by solid preparations), the purity reaches 99%, the yield is not lower than 60%, the fluidity is good, the method conforms to the standards of sucrose auxiliary materials in Chinese pharmacopoeia, and the sucrose crystal is an ideal auxiliary material for a direct-compression solid preparation production method.
It should be understood that the above-described embodiments of the present invention are merely examples for clearly illustrating the present invention, and are not intended to limit the embodiments of the present invention. Other variations and modifications will be apparent to persons skilled in the art in light of the above description. And are neither required nor exhaustive of all embodiments. Any modification, equivalent replacement, and improvement made within the spirit and principle of the present invention should be included in the protection scope of the claims of the present invention.

Claims (10)

1. A novel sucrose refining method with controllable particle size is characterized by comprising the following steps:
s1, dissolving and decoloring: dissolving edible sucrose in deionized water, adding a decolorizing agent, stirring at constant temperature, and filtering to obtain a fine filtrate;
s2, concentrating and crystallizing, namely stirring the fine filtrate obtained in the step S1, concentrating the fine filtrate to form sucrose viscous liquid with the sugar hammer degree of 87 ~ 92 degrees Bx, adding a certain amount of sucrose crystal seeds, stirring and dispersing, and simultaneously opening ultrasonic waves to stimulate the sucrose viscous liquid to crystallize to obtain crystallized liquid;
s3, separation and purification: separating the crystal liquid obtained in the step S2 to obtain coarse crystal grains, adding purified water into the coarse crystal grains, washing and stirring, and performing centrifugal separation to obtain crystal washing grains;
s4, drying and screening: and drying and screening the crystal washing crystal grains obtained in the step S3 to obtain medicinal sucrose crystal grains.
2. The novel sucrose refining method with controllable particle size as claimed in claim 1, wherein the temperature of dissolving food-grade sucrose in deionized water with constant temperature stirring is 75 ~ ℃ and the mass ratio of food-grade sucrose to deionized water is 2 ~: 1.
3. The method of claim 1, wherein the decolorizing agent of S1 is added in an amount of 0.05 ~ 0.1.1% of the food grade sucrose.
4. The novel sucrose refining process with controllable particle size as claimed in claim 1, wherein the decolorizing agent of S1 is injection grade pharmaceutical grade activated carbon.
5. The method as claimed in claim 1, wherein the concentration of the refined solution of S2 is carried out under reduced pressure at 70 ~ 80 deg.C and-0.09 ~ -0.07 MPa.
6. The method of claim 1, wherein the sucrose seed crystals of S2 are added in an amount of 0.1 ~ 0.3.3% by weight of food grade sucrose.
7. The method of claim 1, wherein the frequency of the ultrasonic-stimulated crystallization in S2 is 1500 ~ 1700Hz and the time of the ultrasonic-stimulated crystallization is 20 ~ 30 min.
8. The method of claim 1, wherein the stirring speed of S2 is 22 ~ 35 r/min.
9. The novel sucrose refining process with controllable particle size as claimed in claim 1, wherein the centrifugation top speed of S3 is 1000 ~ 1200 r/min.
10. The method of claim 1, wherein the drying temperature of the washed crystal grains of S4 is 63 ~ 67 ℃.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112090156A (en) * 2020-09-21 2020-12-18 孟州市金玉米有限责任公司 Filtering device for corn starch sugar production and using method
CN113956302A (en) * 2021-11-15 2022-01-21 天津信诚康达药业有限公司 Recrystallization method of medicinal sucrose
CN116143850A (en) * 2022-12-22 2023-05-23 中粮崇左糖业有限公司 Injection-grade sucrose, preparation method and application thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN2072973U (en) * 1990-08-17 1991-03-13 华南理工大学 Solvent/supersonic wave cooperative coring crystallizer
CN105153245A (en) * 2015-09-23 2015-12-16 河南正弘药用辅料有限公司 Production technology for medicinal cane sugar
CN108085424A (en) * 2017-12-29 2018-05-29 天圣制药集团股份有限公司 A kind of preparation method of medical cane sugar
CN108203739A (en) * 2016-12-19 2018-06-26 湖南尔康制药股份有限公司 A kind of process for purification of medical cane sugar

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN2072973U (en) * 1990-08-17 1991-03-13 华南理工大学 Solvent/supersonic wave cooperative coring crystallizer
CN105153245A (en) * 2015-09-23 2015-12-16 河南正弘药用辅料有限公司 Production technology for medicinal cane sugar
CN108203739A (en) * 2016-12-19 2018-06-26 湖南尔康制药股份有限公司 A kind of process for purification of medical cane sugar
CN108085424A (en) * 2017-12-29 2018-05-29 天圣制药集团股份有限公司 A kind of preparation method of medical cane sugar

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
张喜梅等: "声场对蔗糖晶体生长的影响", 《中国甜菜糖业》, no. 04, 30 August 1995 (1995-08-30), pages 14 - 16 *
王立升等: "医药级蔗糖制备工艺研究", 《食品科技》, no. 07, 20 July 2008 (2008-07-20), pages 148 - 150 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112090156A (en) * 2020-09-21 2020-12-18 孟州市金玉米有限责任公司 Filtering device for corn starch sugar production and using method
CN113956302A (en) * 2021-11-15 2022-01-21 天津信诚康达药业有限公司 Recrystallization method of medicinal sucrose
CN116143850A (en) * 2022-12-22 2023-05-23 中粮崇左糖业有限公司 Injection-grade sucrose, preparation method and application thereof
CN116143850B (en) * 2022-12-22 2023-12-15 中粮崇左糖业有限公司 Injection-grade sucrose, preparation method and application thereof

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