CN109851682A - A kind of carboxymethyl-modification method of bean dregs dietary fiber and products thereof - Google Patents

A kind of carboxymethyl-modification method of bean dregs dietary fiber and products thereof Download PDF

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Publication number
CN109851682A
CN109851682A CN201811629416.4A CN201811629416A CN109851682A CN 109851682 A CN109851682 A CN 109851682A CN 201811629416 A CN201811629416 A CN 201811629416A CN 109851682 A CN109851682 A CN 109851682A
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dietary fiber
carboxymethyl
bean dregs
vacuum filter
solid matter
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郑志
廉梦云
李兴江
罗水忠
赵妍嫣
姜绍通
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Hefei University of Technology
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Hefei University of Technology
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Abstract

A kind of carboxymethyl-modification method of bean dregs dietary fiber, including pretreatment, the processing of NaOH/ urea liquid, centrifugal treating, carboxy methylation processing, washing and drying and crushing.The degree of substitution by carboxymethyl of carboxymethyl bean dregs dietary fiber produced by the present invention is 0.40-0.55, solubility 75-85%.

Description

A kind of carboxymethyl-modification method of bean dregs dietary fiber and products thereof
Technical field
The present invention relates to a kind of carboxymethyl-modification methods of bean dregs dietary fiber and products thereof, belong to deep processing of farm products Technical field.
Background technique
Soybean, also known as soya bean, originate in China, cultivate extensively in all over the world at present.Soybean is the important grain in China One of crop has 5,000 years cultivation histories, and Gu claims bean, is a kind of crop that its seed contains abundant phytoprotein.Soybean Various bean product are most commonly used for, soya-bean oil is squeezed, make soy sauce and extracts protein.
Bean dregs are the byproducts during Soybean production soymilk, soya-bean milk, bean curd, contain protein, fat, calcium, phosphorus, iron etc. A variety of nutriments.China be bean curd, soya-bean milk production cradle, have long production history, bean curd, soya-bean milk production, Sales volume is all larger, and corresponding bean dregs yield is also very big.General bean dregs water content 85%, protein 3.0%, fat 0.5%, carbon water Compound 8.0% etc., wherein the main component of carbohydrate is dietary fiber.In bean dregs dietary fiber, about 40% is cellulose.
Cellulose be it is a kind of by glucose group at macromolecular substances, mainly from green plants, be that plant fiber is thin The important component of cell wall, therefore, cellulose are the renewable resources of rich reserves in nature.In recent years, with scientific and technological progress, Cellulose is also applied to the new neck such as biological medicine, petrochemical industry in addition to applying as raw material in fields such as food, papermaking Domain.
Carboxymethyl cellulose is a kind of critically important anionic cellulose ether, water-soluble, has thickening, stablizes, parent The effects of water, gelation, tool has been widely used.Carboxymethyl cellulose is replaced by carboxymethyl fine by alkalization, etherification process Prepared by the hydroxyl on dimension element.Cellulose, hemicellulose in bean dregs dietary fiber contain activity hydroxy, can also introduce carboxylic first Base is modified, and the property of dietary fiber can be improved to a certain extent.Traditional basification is to be with water or organic solvent The problems such as reaction medium causes complex process, at high cost, is easy pollution environment.Therefore exploring novel reaction medium is that science is ground The developing direction studied carefully.
Summary of the invention
The purpose of the present invention is to provide a kind of carboxymethyl-modification methods of bean dregs dietary fiber and products thereof.
In order to achieve the above objects and other related objects, present invention provide the technical scheme that a kind of bean dregs dietary fiber Carboxymethyl-modification method, including the following steps:
Step 1: mixing bean dregs dietary fiber with purified water 1:0.8-1.5 in mass ratio under the conditions of 5-30 DEG C, 60- is impregnated 120min;Then using refiner handle 2-4 time, the time per treatment be 2-4min, twice handle between interval time be 2-4min;Material after homogenized is placed in steam blasting equipment, handles 120-180s with the steam dimension pressure of 1.8-2.0Mpa, It is then shut off high steam, opens material liquid outlet valve, material sprays, and explosion occurs under the action of pressure difference;Collect explosion Material after processing, it is spare;
Step 2: the material and NaOH/ urea liquid after the steam blasting for obtaining the first step are by quality at a temperature of 5-30 DEG C It is mixed than 5-10:100 ratio, then with revolving speed 30-60r/min stir process 15-30min;During stir process, make to mix It closes material to be in ultrasonic environment, ultrasonic frequency 25-35KHz, power density 0.35-0.45w/cm2;Stir process After mixed material is placed on to 15-16h in -20.5-19.5 DEG C of low temperature environment;
Step 3: the mixed material that second step is obtained is centrifuged under conditions of 0-6 DEG C with the revolving speed of 7000-8000r/min 15-18min obtains supernatant;
Step 4: the supernatant is placed in 33-37 DEG C of water-bath, sodium chloroacetate is added after stirring 10-15min, then It is warming up to 53-57 DEG C, keeps the temperature 60-65min;It is warming up to 65-70 DEG C again, keeps the temperature 60-65min, is finally added into reaction system The volume fraction of 3.0-3.5 times of its volume is the ethyl alcohol of 95-98%, then terminates reaction, is stood to accumulate sediment;
Step 5: the mixture that the 4th step obtains is placed in progress vacuum filter processing in vacuum filter, collection obtains first Solid matter is retained, then the first retention solid matter is washed and filtration treatment three times;
S1, for the first time washing and filtration treatment
First retention solid matter is mixed with 25-30 times of its quality of purified water, then agitation cleaning, then sets mixture Vacuum filter processing is carried out in vacuum filter, collection obtains the second retention solid matter;
S2, second of washing and filtration treatment
Second retention solid matter is mixed with the ethyl alcohol that 15-20 times of its quality of volume fraction is 70-80%, then agitation is clear It washes, mixture is then placed in progress vacuum filter processing in vacuum filter, collection obtains third retention solid matter;
S3, third time washing and filtration treatment
Third retention solid matter is mixed with the ethyl alcohol that 8-10 times of its quality of volume fraction is 95-98%, then agitation is clear It washes, mixture is then placed in progress vacuum filter processing in vacuum filter, collection obtains the 4th retention solid matter;
Step 6: the 4th retention solid matter is less than or equal to 8% using 60-80 DEG C of heated-air drying to water content, it is crushed to Up to carboxymethyl bean dregs dietary fiber product after 60-100 mesh.
Preferred technical solution are as follows: the water content of the bean dregs dietary fiber is 6-8%, and dietary fiber purity is 85-90%, Fineness is 60-100 mesh.
Preferred technical solution are as follows: the shearing rotating speed of the refiner is 8000-13000r/min.
Preferred technical solution are as follows: for the NaOH/ urea liquid using purified water as solvent, NaOH, urea are solute to match Solution is set, so that the mass concentration of NaOH is the mass concentration 4-12% of 6-7%, urea in solution.
Preferred technical solution are as follows: negative pressure of vacuum when vacuum filter processing is carried out in the 5th step, in vacuum filter For 0.4-0.5MPa, aperture of filter screen 30-50mm.
Preferred technical solution are as follows: in S1, the negative pressure of vacuum in vacuum filter when progress vacuum filter processing is 0.4-0.5MPa, aperture of filter screen 30-50mm.
Preferred technical solution are as follows: in S2, the negative pressure of vacuum in vacuum filter when progress vacuum filter processing is 0.7-0.8MPa, aperture of filter screen 3-5mm.
Preferred technical solution are as follows: negative pressure of vacuum when vacuum filter processing is carried out in the 5th step, in vacuum filter For 0.7-0.8MPa, aperture of filter screen 3-5mm.
Preferred technical solution are as follows: the additive amount of the sodium chloroacetate is the 8-12% of supernatant quality.
In order to achieve the above objects and other related objects, present invention provide the technical scheme that a kind of bean dregs dietary fiber Carboxymethyl-modification product, the carboxymethyl-modification product of the bean dregs dietary fiber is fine according to the above-mentioned bean dregs diet of right The carboxymethyl-modification method of dimension is made, degree of substitution by carboxymethyl 0.40-0.55, solubility 75-85%.
Since above-mentioned technical proposal is used, the present invention has the advantage, that compared with prior art
The degree of substitution by carboxymethyl of carboxymethyl bean dregs dietary fiber produced by the present invention is 0.40-0.55, solubility 75-85%.
Detailed description of the invention
Fig. 1 is the FTIR spectrogram of bean dregs dietary fiber and carboxymethyl-modification bean dregs dietary fiber.
Specific embodiment
Embodiments of the present invention are illustrated by particular specific embodiment below, those skilled in the art can be by this implementation Content disclosed by example is understood other advantages and efficacy of the present invention easily.
The purpose of term used herein, which is only that, illustrates particular embodiment, it is not intended to be limited to the present invention.It removes Non- context is explicitly shown, otherwise singular " one " used herein, "one" also include plural form.
When illustrating preferred embodiment, it is potentially based on clear purpose and uses special term;However, this specification institute Revealer is not intended to be limited in the selected special term;And it is to be understood that each particular element includes having Identical function, all equivalence techniques for operating in a similar manner and reaching similar effects.
Embodiment one: a method of extracting cellulose from bean dregs dietary fiber
A method of it extracting cellulose from bean dregs dietary fiber, includes the following steps.
(1) it pre-processes
The bean dregs dietary fiber is made using new fresh bean dreg as raw material by proteolysis, decoloration washing, dry, crushing.Institute The bean dregs dietary fiber stated, water content 7m%, dietary fiber purity are 83m%, and fineness is 80 mesh.
At a temperature of 20 DEG C, bean dregs dietary fiber is mixed with food-grade purified water 1:1 in mass ratio, impregnates 90min;It adopts It is handled 3 times, each shearing rotating speed 10000r/min with food-grade refiner, handles time 3min, intermittent time per treatment 3min。
Material after homogenized is placed in steam blasting equipment, ties up pressure processing 160s with 1.9MPa steam;Then, it closes High steam is closed, material liquid outlet valve is opened, material sprays, and explosion occurs under the action of pressure difference and temperature difference;It collects quick-fried Material after tear reason, it is spare.
(2) NaOH/ urea liquid is handled
It is made into NaOH/ urea liquid.Using food-grade purified water as solvent, NaOH, urea are solute to configure solution, so that solution In, NaOH mass concentration is 6.5m%, urea quality concentration 8m%.
At a temperature of 20 DEG C, by after steam blasting material and NaOH/ urea liquid 7.5:100 ratio in mass ratio mix It closes, revolving speed 45r/min stir process 25min;During stir process, it is in mixed material in ultrasonic environment, ultrasonic wave Frequency is 30KHz, power density 0.4w/cm2.After stir process, mixed material is placed in -20 DEG C of low temperature environments 15.5h。
(3) centrifugal treating
Mixed material in low temperature environment is taken out, at a temperature of 3 DEG C, 16.5min is centrifuged using revolving speed 7500r/min, obtains Supernatant, it is spare.
(4) carboxy methylation is handled
The supernatant that centrifugation obtains is placed in 35 DEG C of water-baths, 12min is stirred;Sodium chloroacetate is slowly added to its mass concentration (i.e. using supernatant as solvent, sodium chloroacetate is solute, and the concentration of the solution of formation is 10%) to reach 10m%, and system is warming up to 55 DEG C, keep the temperature 62min;System is warming up to 68 DEG C again, keeps the temperature 62min;Then, 3.2 times of its volume is added into reaction solution 95% ethyl alcohol, terminate reaction, formed and stand accumulation sediment.
(5) washing and drying and crushing
The mixture of reaction solution, ethyl alcohol, sediment is placed in vacuum filter, in negative pressure of vacuum 0.45MPa, opening of sieve Vacuum filter is handled under conditions of diameter 40mm, collects the solid matter of retention.To the solid matter of retention carry out washing three times and Filtration treatment.
Washing and filtration treatment for the first time.The food-grade purified water of 27 times of quality is mixed with the solid matter of retention, is stirred Mixture, is then placed in vacuum filter, under conditions of negative pressure of vacuum 0.45MPa, aperture of filter screen 40mm by dynamic cleaning Vacuum filter processing, collects the solid matter of retention.
Second of washing and filtration treatment.What is retained after the ethyl alcohol that 17 times of volume fractions are 75% is filtered with first time consolidates Mixture, is then placed in vacuum filter, in negative pressure of vacuum 0.7MPa, aperture of filter screen by body material mixing, agitation cleaning Vacuum filter is handled under conditions of 3mm, collects the solid matter of retention.
Third time washing and filtration treatment.The solid retained after the ethyl alcohol that 9 times of volume fractions are 75% is filtered with second Mixture, is then placed in vacuum filter, in negative pressure of vacuum 0.7MPa, aperture of filter screen 3mm by material mixing, agitation cleaning Under conditions of vacuum filter handle, collect the solid matter of retention.
Will third time filtering retention solid matter use 70 DEG C of heated-air dryings most 7%, be then crushed to 80 mesh to get To carboxymethyl bean dregs dietary fiber product, the FTIR spectrogram of carboxymethyl-modification bean dregs dietary fiber as shown in Figure 1, in figure, The line of the top in left side is that carboxymethyl-modification bean dregs dietary fiber, lower section is bean dregs dietary fiber.
The carboxymethyl-modification product of the bean dregs dietary fiber, degree of substitution by carboxymethyl 0.5, solubility 80%.
Embodiment two: a method of extracting cellulose from bean dregs dietary fiber
A method of extracting cellulose from bean dregs dietary fiber, including the following steps:
Step 1: mixing bean dregs dietary fiber with purified water 1:1.5 in mass ratio under the conditions of 30 DEG C, 120min is impregnated; Then it is handled 4 times using refiner, the time per treatment is 4min, and the interval time between processing is 4min twice;At homogenate Material after reason is placed in steam blasting equipment, with the steam dimension pressure processing 180s of 2.0Mpa, is then shut off high steam, is opened Material liquid outlet valve, material spray, and explosion occurs under the action of pressure difference;Material after collection explosion treatment, it is spare;
Step 2: material and NaOH/ urea liquid after the steam blasting for obtaining the first step are in mass ratio at a temperature of 30 DEG C 10:100 ratio mixing, then with revolving speed 60r/min stir process 30min;During stir process, it is in mixed material In ultrasonic environment, ultrasonic frequency 35KHz, power density 0.45w/cm2;Mixed material is put after stir process Set the 16h in -19.5 DEG C of low temperature environment;
Step 3: the mixed material that second step is obtained is centrifuged 18min with the revolving speed of 8000r/min, obtains under conditions of 6 DEG C To supernatant;
Step 4: the supernatant is placed in 37 DEG C of water-bath, sodium chloroacetate is added after stirring 15min, then heats to 57 DEG C, keep the temperature 65min;It is warming up to 70 DEG C again, keeps the temperature 65min, the volume point of 3.5 times of its volume is finally added into reaction system Then the ethyl alcohol that number is 98% terminates reaction, stand to accumulate sediment;
Step 5: the mixture that the 4th step obtains is placed in progress vacuum filter processing in vacuum filter, collection obtains first Solid matter is retained, then the first retention solid matter is washed and filtration treatment three times;
S1, for the first time washing and filtration treatment
First retention solid matter is mixed with 30 times of its quality of purified water, then mixture, is then placed in by agitation cleaning Vacuum filter processing is carried out in vacuum filter, collection obtains the second retention solid matter;
S2, second of washing and filtration treatment
Second retention solid matter is mixed with the ethyl alcohol that 20 times of its quality of volume fraction is 80%, then agitation cleaning, then Mixture is placed in progress vacuum filter processing in vacuum filter, collection obtains third retention solid matter;
S3, third time washing and filtration treatment
Third retention solid matter is mixed with the ethyl alcohol that 10 times of its quality of volume fraction is 98%, then agitation cleaning, then Mixture is placed in progress vacuum filter processing in vacuum filter, collection obtains the 4th retention solid matter;
Step 6: using 80 DEG C of heated-air drying for 6%, to be crushed to after 100 mesh to obtain the final product to water content the 4th retention solid matter To soybean-drag fiber element product.
Preferred technical solution are as follows: the water content of the bean dregs dietary fiber is 8%, and dietary fiber purity is 90%, fineness For 100 mesh.
Preferred technical solution are as follows: the shearing rotating speed of the refiner is 13000r/min.
Preferred technical solution are as follows: for the NaOH/ urea liquid using purified water as solvent, NaOH, urea are solute to match Solution is set, so that the mass concentration of NaOH is the mass concentration 12% of 7%, urea in solution.
Preferred technical solution are as follows: negative pressure of vacuum when vacuum filter processing is carried out in the 5th step, in vacuum filter For 0.5MPa, aperture of filter screen 50mm.
Preferred technical solution are as follows: in S1, the negative pressure of vacuum in vacuum filter when progress vacuum filter processing is 0.5MPa, aperture of filter screen 50mm.
Preferred technical solution are as follows: in S2, the negative pressure of vacuum in vacuum filter when progress vacuum filter processing is 0.8MPa, aperture of filter screen 5mm.
Preferred technical solution are as follows: negative pressure of vacuum when vacuum filter processing is carried out in the 5th step, in vacuum filter For 0.8MPa, aperture of filter screen 5mm.
The carboxymethyl-modification product of the bean dregs dietary fiber, degree of substitution by carboxymethyl 0.55, solubility 85%.
Embodiment three: a method of extracting cellulose from bean dregs dietary fiber
A method of extracting cellulose from bean dregs dietary fiber, including the following steps:
Step 1: mixing bean dregs dietary fiber with purified water 1:0.8 in mass ratio under the conditions of 5 DEG C, 60min is impregnated;Then It is handled 2 times using refiner, the time per treatment is 2min, and the interval time between processing is 2min twice;After homogenized Material be placed in steam blasting equipment, with the steam of 1.8Mpa dimension pressure processing 120s, be then shut off high steam, open feed liquid Outlet valve, material spray, and explosion occurs under the action of pressure difference;Material after collection explosion treatment, it is spare;
Step 2: material and NaOH/ urea liquid after the steam blasting for obtaining the first step are in mass ratio at a temperature of 5 DEG C 5:100 ratio mixing, then with revolving speed 30r/min stir process 15min;During stir process, it is in mixed material In ultrasonic environment, ultrasonic frequency 25KHz, power density 0.35w/cm2;Mixed material is put after stir process Set the 15h in -20.5 DEG C of low temperature environment;
Step 3: the mixed material that second step is obtained is centrifuged 15min with the revolving speed of 7000r/min, obtains under conditions of 0 DEG C To supernatant;
Step 4: the supernatant is placed in 33 DEG C of water-bath, sodium chloroacetate is added after stirring 10min, then heats to 53 DEG C, keep the temperature 60min;It is warming up to 65 DEG C again, keeps the temperature 60min, the volume point of 3.0 times of its volume is finally added into reaction system Then the ethyl alcohol that number is 95% terminates reaction, stand to accumulate sediment;
Step 5: the mixture that the 4th step obtains is placed in progress vacuum filter processing in vacuum filter, collection obtains first Solid matter is retained, then the first retention solid matter is washed and filtration treatment three times;
S1, for the first time washing and filtration treatment
First retention solid matter is mixed with 25 times of its quality of purified water, then mixture, is then placed in by agitation cleaning Vacuum filter processing is carried out in vacuum filter, collection obtains the second retention solid matter;
S2, second of washing and filtration treatment
Second retention solid matter is mixed with the ethyl alcohol that 15 times of its quality of volume fraction is 70%, then agitation cleaning, then Mixture is placed in progress vacuum filter processing in vacuum filter, collection obtains third retention solid matter;
S3, third time washing and filtration treatment
Third retention solid matter is mixed with the ethyl alcohol that 8 times of its quality of volume fraction is 95%, then agitation cleaning, then Mixture is placed in progress vacuum filter processing in vacuum filter, collection obtains the 4th retention solid matter;
Step 6: using 60 DEG C of heated-air drying for 5%, to be crushed to after 60 mesh to obtain the final product to water content the 4th retention solid matter To soybean-drag fiber element product.
Preferred technical solution are as follows: the water content of the bean dregs dietary fiber is 6%, and dietary fiber purity is 85%, fineness For 60 mesh.
Preferred technical solution are as follows: the shearing rotating speed of the refiner is 8000r/min.
Preferred technical solution are as follows: for the NaOH/ urea liquid using purified water as solvent, NaOH, urea are solute to match Solution is set, so that the mass concentration of NaOH is the mass concentration 4% of 6%, urea in solution.
Preferred technical solution are as follows: negative pressure of vacuum when vacuum filter processing is carried out in the 5th step, in vacuum filter For 0.4MPa, aperture of filter screen 30mm.
Preferred technical solution are as follows: in S1, the negative pressure of vacuum in vacuum filter when progress vacuum filter processing is 0.4MPa, aperture of filter screen 30mm.
Preferred technical solution are as follows: in S2, the negative pressure of vacuum in vacuum filter when progress vacuum filter processing is 0.7MPa, aperture of filter screen 3mm.
Preferred technical solution are as follows: negative pressure of vacuum when vacuum filter processing is carried out in the 5th step, in vacuum filter For 0.7MPa, aperture of filter screen 3mm.
The carboxymethyl-modification product of the bean dregs dietary fiber, degree of substitution by carboxymethyl 0.40, solubility 75%.
As described above is only to be not intended to tool to explain the preferred embodiments of the invention to do any shape to the present invention Limitation in formula should all wrap therefore all have any modification or change for making the related present invention under identical spirit It includes in the scope that the invention is intended to protect.

Claims (10)

1. a kind of carboxymethyl-modification method of bean dregs dietary fiber, it is characterised in that: include the following steps:
Step 1: mixing bean dregs dietary fiber with purified water 1:0.8-1.5 in mass ratio under the conditions of 5-30 DEG C, 60- is impregnated 120min;Then using refiner handle 2-4 time, the time per treatment be 2-4min, twice handle between interval time be 2-4min;Material after homogenized is placed in steam blasting equipment, handles 120-180s with the steam dimension pressure of 1.8-2.0Mpa, It is then shut off high steam, opens material liquid outlet valve, material sprays, and explosion occurs under the action of pressure difference;Collect explosion Material after processing, it is spare;
Step 2: the material and NaOH/ urea liquid after the steam blasting for obtaining the first step are by quality at a temperature of 5-30 DEG C It is mixed than 5-10:100 ratio, then with revolving speed 30-60r/min stir process 15-30min;During stir process, make to mix It closes material to be in ultrasonic environment, ultrasonic frequency 25-35KHz, power density 0.35-0.45w/cm2;Stir process After mixed material is placed on to 15-16h in -20.5-19.5 DEG C of low temperature environment;
Step 3: the mixed material that second step is obtained is centrifuged under conditions of 0-6 DEG C with the revolving speed of 7000-8000r/min 15-18min obtains supernatant;
Step 4: the supernatant is placed in 33-37 DEG C of water-bath, sodium chloroacetate is added after stirring 10-15min, then It is warming up to 53-57 DEG C, keeps the temperature 60-65min;It is warming up to 65-70 DEG C again, keeps the temperature 60-65min, is finally added into reaction system The volume fraction of 3.0-3.5 times of its volume is the ethyl alcohol of 95-98%, then terminates reaction, is stood to accumulate sediment;
Step 5: the mixture that the 4th step obtains is placed in progress vacuum filter processing in vacuum filter, collection obtains first Solid matter is retained, then the first retention solid matter is washed and filtration treatment three times;
S1, for the first time washing and filtration treatment
First retention solid matter is mixed with 25-30 times of its quality of purified water, then agitation cleaning, then sets mixture Vacuum filter processing is carried out in vacuum filter, collection obtains the second retention solid matter;
S2, second of washing and filtration treatment
Second retention solid matter is mixed with the ethyl alcohol that 15-20 times of its quality of volume fraction is 70-80%, then agitation is clear It washes, mixture is then placed in progress vacuum filter processing in vacuum filter, collection obtains third retention solid matter;
S3, third time washing and filtration treatment
Third retention solid matter is mixed with the ethyl alcohol that 8-10 times of its quality of volume fraction is 95-98%, then agitation is clear It washes, mixture is then placed in progress vacuum filter processing in vacuum filter, collection obtains the 4th retention solid matter;
Step 6: the 4th retention solid matter is less than or equal to 8% using 60-80 DEG C of heated-air drying to water content, it is crushed to Up to carboxymethyl bean dregs dietary fiber product after 60-100 mesh.
2. the carboxymethyl-modification method of bean dregs dietary fiber according to claim 1, it is characterised in that: the bean dregs meals The water content for eating fiber is 6-8%, and dietary fiber purity is 85-90%, and fineness is 60-100 mesh.
3. the carboxymethyl-modification method of bean dregs dietary fiber according to claim 1, it is characterised in that: the refiner Shearing rotating speed be 8000-13000r/min.
4. the carboxymethyl-modification method of bean dregs dietary fiber according to claim 1, it is characterised in that: the NaOH/ Urea liquid is using purified water as solvent, and NaOH, urea are solute to configure solution, so that in solution, the mass concentration of NaOH is The mass concentration 4-12% of 6-7%, urea.
5. the carboxymethyl-modification method of bean dregs dietary fiber according to claim 1, it is characterised in that: in the 5th step In, in vacuum filter carry out vacuum filter processing when negative pressure of vacuum be 0.4-0.5MPa, aperture of filter screen 30-50mm.
6. the carboxymethyl-modification method of bean dregs dietary fiber according to claim 1, it is characterised in that: in S1, very In empty filter carry out vacuum filter processing when negative pressure of vacuum be 0.4-0.5MPa, aperture of filter screen 30-50mm.
7. the carboxymethyl-modification method of bean dregs dietary fiber according to claim 1, it is characterised in that: in S2, very In empty filter carry out vacuum filter processing when negative pressure of vacuum be 0.7-0.8MPa, aperture of filter screen 3-5mm.
8. the carboxymethyl-modification method of bean dregs dietary fiber according to claim 1, it is characterised in that: in the 5th step In, in vacuum filter carry out vacuum filter processing when negative pressure of vacuum be 0.7-0.8MPa, aperture of filter screen 3-5mm.
9. the carboxymethyl-modification method of bean dregs dietary fiber according to claim 1, it is characterised in that: the monoxone The additive amount of sodium is the 8-12% of supernatant quality.
10. a kind of carboxymethyl-modification product of bean dregs dietary fiber, it is characterised in that: the carboxymethyl of the bean dregs dietary fiber Change modified product according to the carboxymethyl-modification method system of bean dregs dietary fiber described in claim 1-9 any claim , degree of substitution by carboxymethyl 0.40-0.55, solubility 75-85%.
CN201811629416.4A 2018-12-28 2018-12-28 A kind of carboxymethyl-modification method of bean dregs dietary fiber and products thereof Pending CN109851682A (en)

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* Cited by examiner, † Cited by third party
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CN110786448A (en) * 2019-11-14 2020-02-14 合肥工业大学 Dough added with high-water-holding-capacity modified bran dietary fiber and preparation method thereof
CN113057340A (en) * 2021-04-29 2021-07-02 南京邮电大学 Method for modifying mushroom dietary fiber
CN113057340B (en) * 2021-04-29 2024-01-19 南京邮电大学 Mushroom dietary fiber modification method

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Application publication date: 20190607