CN106316784B - A method of xylitol is prepared with oil tea shell - Google Patents

A method of xylitol is prepared with oil tea shell Download PDF

Info

Publication number
CN106316784B
CN106316784B CN201610698186.1A CN201610698186A CN106316784B CN 106316784 B CN106316784 B CN 106316784B CN 201610698186 A CN201610698186 A CN 201610698186A CN 106316784 B CN106316784 B CN 106316784B
Authority
CN
China
Prior art keywords
oil tea
tea shell
weight
spare
xylitol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201610698186.1A
Other languages
Chinese (zh)
Other versions
CN106316784A (en
Inventor
管天球
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hunan Yougu Hi Tech Co ltd
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CN201610698186.1A priority Critical patent/CN106316784B/en
Publication of CN106316784A publication Critical patent/CN106316784A/en
Application granted granted Critical
Publication of CN106316784B publication Critical patent/CN106316784B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C07C29/136Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
    • C07C29/14Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group
    • C07C29/141Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group with hydrogen or hydrogen-containing gases
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P19/00Preparation of compounds containing saccharide radicals
    • C12P19/02Monosaccharides

Abstract

(1), sorting a kind of method preparing xylitol with oil tea shell disclosed by the invention, is related to biomedicine technical field, preparation process is as follows:;(2), impregnate;(3), dry;(4), crush;(5), ferment;(6), homogeneous;(7), hydrolyze;(8), digest;(9), decolourize;(10), neutralize;(11), mix;(12), column is crossed;(13), it is concentrated;(14), freeze;(15), hydrogenate;(16), crystallize.Have the characteristics that raw material sources are wide, production cost is low, superior product quality, be suitable for preparing xylitol with oil tea shell, it can also be used to prepare xylitol with agricultural crops such as corncob, bagasse.

Description

A method of xylitol is prepared with oil tea shell
Technical field
The present invention relates to biomedicine technical field, especially a kind of method for preparing xylitol with oil tea shell.
Background technique
Xylitol is the normal intermediate of a kind of sweet substance with nutritive value and human body carbohydate metabolism.Certainly In right boundary, xylitol is widely present in various water fruits and vegetables, but content is very low.Currently, commodity xylitol is using jade mostly In the agricultural crops such as meter Xin, bagasse, deacidifying process and ion are neutralized by prepared by deep processing, extraction process mainly has Exchange deacidifying process.
It neutralizes deacidifying process process are as follows: raw material → hydrolysis → neutralization → concentration → decoloration → ion exchange → concentration → add Hydrogen → concentration → crystallization → separation → packaging.
Its ion exchange deacidifying process process are as follows: raw material → hydrolysis → decoloration → ion exchange → concentration → ion exchange → Add hydrogen → ion exchange → concentration → crystallization → separation → packaging.
Oil tea shell is that camellia oleifera fruit separates the epidermis shell after tea seed, contains Tea Saponin, tea seed polysaccharide, tea seed in oil tea shell The active material of the utility values such as albumen.Currently, in most of rural area and mountain area, oil tea shell is not that be dropped be exactly to be used to fire Burning take it is slow, it is a small amount of to be used to prepare activated carbon, thus, not only waste of resource, but also pollution environment.
It is " a kind of to prepare xylitol using tea fruit shell disclosed in Chinese patent (number of patent application 201510488115.4) Method ", preparation process include: to use sulphuric acid hydrolysis after raw tea material shell crushes, and gained hydrolyzate uses CaCO again3During lotion carries out With obtain liquid glucose, with active carbon decoloring after the concentration of gained liquid glucose, liquid glucose further purified by ion exchange, finally using hot Band Candida carries out bioconversion and obtains xylitol.
Summary of the invention
That the purpose of the present invention is to provide a kind of raw material sources is wide, production cost is low, the preparation of the xylitol of superior product quality Method.
To achieve the above object, technical measures adopted by the present invention are to invent a kind of side that xylitol is prepared with oil tea shell Method, preparation process are as follows:
(1), sorting: selection nothing is rotted, without mildew, no disease and pests harm, fresh oil tea shell, spare;
(2), impregnate: by oil tea shell be put into 2-5 times of weight, volumetric concentration be 75-85% edible ethanol in, it is normal in room temperature 8-20h is impregnated in pressure, filters off soak, 2-5 times of weight is added, the edible ethanol that volumetric concentration is 35-50%, in 45-55 30-50min is impregnated at DEG C, is filtered, and is collected and is impregnated oil tea shell, it is spare;
(3), dry: oil tea shell will be impregnated and be transferred in baking oven, dry under 65-70 DEG C, normal pressure to water content and be less than 8%, dry oil tea shell is obtained, it is spare;
(4), crush: and then dry oil tea shell is ground into the oil tea shell particle of 5-20 mesh, it is spare;
(5), ferment: being added into oil tea shell particle and account for its weight 25-35%, the water that temperature is 35-40 DEG C, be added simultaneously The leavening for accounting for crude oil tea shell weight 8-15.5% is sealed by fermentation processing 1-3 days at 28-35 DEG C, becomes fermentation oil tea shell Grain, it is spare;
(6), homogeneous: being processed into uniform fermentation oil tea shell material through homogenizer at normal temperature for fermentation oil tea shell particle, standby With;
(7), hydrolyze: being added and crude oil tea shell particle identical weight, weight concentration 1.5- into fermentation oil tea shell material 3.0% sour water, stirs evenly, and is heated to 110-140 DEG C by the heating rate of 5-10 DEG C/min, heats while stirring, then exists Pressure is to handle 2.5-4.0h under 1.25-1.5MPa;Thereafter, when being naturally cooling to 70-80 DEG C, oil tea shell is collected in filtering respectively Hydrolyzate and oil tea shell slag, it is spare;
(8), digest: the buck that oil tea shell slag clear water or weight concentration are 0.5-1.5% being cleaned 2-3 times, is drained;Again Calcium sulfate, the 0.2- for accounting for the zytase of its weight 1.2-2.5%, the papain of 0.1-0.5%, 0.5-1.2% is added 1.0% magnesium phosphate mixes, the encapsulation process 20-38h at 20-30 DEG C;Then it is added and accounts for 2-3 times of oil tea shell slag weight, 40- 50 DEG C of warm water handles 20-40min, and filtering collects oil tea shell slag and digests Aqueous extracts, spare;
(9), decolourize: the decolorising agent for accounting for its weight 15-25% being added into oil tea shell hydrolyzate, at 70-80 DEG C at stirring Reason, stirring rate 50-60r/min, when the light transmittance of oil tea shell hydrolyzate reaches 85% or more, oil tea shell is collected in filtering Decolourize hydrolyzate, spare;
(10), neutralizing: being slowly added to the buck that weight concentration is 5-10% into oil tea shell decoloration hydrolyzate, side edged stirs, When the pH value of oil tea shell decoloration hydrolyzate reaches 6.0-6.5, oil tea shell neutralizing hydrolysis liquid is obtained, it is spare;
(11), mix: oil tea shell slag being digested into Aqueous extracts and oil tea shell neutralizing hydrolysis liquid mixes, it is naturally quiet to put 4- after stirring evenly 8h, filtering, obtains oil tea shell mixed hydrolysis liquid, spare;
(12), cross column: oil tea shell mixed hydrolysis liquid is heated to 35-45 DEG C, cross anion exchange resin while hot, flow velocity is 15-28L/h collects anion exchange resin and crosses column liquid;Then anion exchange resin is crossed into column liquid and crosses cation exchange resin, Flow velocity is 10-20L/h, collects cation exchange resin and crosses column liquid;Cation exchange resin is crossed into column liquid again and is heated to 50-60 DEG C, S-330 type macroporous absorbent resin is crossed, flow velocity 35-50L/h collects macroporous absorbent resin and crosses column liquid, spare;
(13), be concentrated: by macroporous absorbent resin cross column liquid investment inspissator in, temperature be 50-60 DEG C, pressure 1-5KPa Under conditions of, the 1/8-1/5 of concentration to original volume obtains concentrated column liquid, spare;
(14), freeze: concentrated column liquid is transferred in freezer, quiet at 0-6 DEG C to put 5-8h, supernatant liquid is collected in filtering; The edible ethanol that volumetric concentration is 90% or more is slowly added into supernatant liquid again, keeps the volume of the ethyl alcohol in supernatant liquid dense Degree reaches 45-65%, then, quiet in freezer to put to no Precipitation, filtering, collects precipitating, spare;
(15), hydrogenate: the clear water of precipitating equivalent weight is dissolved, while the hydrogenating catalytic for accounting for Sediment weight 3-5% is added Agent stirs evenly;Then pressure is 5-10MPa, temperature is 120-150 DEG C, the rate that is passed through of hydrogen is 1-2.5m3It is handled under/h 60-75min, the xylitol liquid after must hydrogenating are spare;
(16), crystallize: xylitol liquid is transferred in freezer, while the edible ethanol for being 95% or more with volumetric concentration is adjusted Concentration of alcohol in xylitol liquid is 65% or more, then, quiet to put to no Precipitation, filtering, collects xylitol precipitating;So Afterwards, it by xylitol precipitating deionized water dissolving, filters, then through drying, crushing to get xylitol.
Leavening described in fermentation procedure can be cellulase or saccharomycete, be also possible to by calcium sulfate, sorghum flour, Cellulase, saccharomycete press (0.2-0.35): the weight ratio of (4-6): 0.2:1 mixes.
Sour water described in hydrolyzing process is one of hydrochloric acid, sulfuric acid, oxalic acid or a variety of aqueous solutions, when for two kinds with When upper, it parts by weight or other ratios such as the ratio of each component is.
In hydrolyzing process, heat while stirring, stirring rate 15-25r/min.
Decolorising agent described in bleaching process can be neutral active charcoal particle or neutral diatomite or silica gel, be also possible to By neutral active charcoal particle, neutral diatomite, 80-120 mesh silica gel by 1:(1-1.5): the weight ratio of (0.3-0.45) is matched System mixes.
Buck described in neutralization step is one of sodium hydroxide, calcium hydroxide, sodium carbonate or a variety of aqueous solutions, When to be two or more, it parts by weight or other ratios such as the ratio of each component is.
Anion exchange resin is strong-base anion-exchange resin or other anion exchange resin, cation exchange Resin is weak-acid cation-exchange resin or other cation exchange resins.
The method for preparing xylitol with oil tea shell of the invention is using discarded oil tea shell as raw material, thus, original Expect that source is wide.Meanwhile enzymatic hydrolysis process is devised in addition, the further loose fibre structure of oil tea shell, so that hydrolysis effect is more Thoroughly, more efficient, product extracting rate is higher, and production cost is relatively low.In addition, using the second of various concentration in process early period Alcohol processing, reduces the content of such as Tea Saponin, tea polysaccharide, tea albumen, avoids its influence to subsequent operation;And crossing column work Two step resin treatments are taken in sequence, efficiently eliminate remaining impurity, avoid the influence to product appearance and subsequent operation, therefore Prepared product quality is preferable.
Following table 1 is the effective ingredient detection data using xylitol prepared by method of the invention:
Table 1 (content of 100g)
Composition Content (g)
Xylitol 96.52
Xylose 1.125
Glucose 0.562
Polysaccharide 0.025
It can be seen that from upper table data using xylitol prepared by method of the invention, content is high, quality is good, is suitble to The application in each field.
Specific embodiment
With reference to embodiments, the present invention is further illustrated.Following explanation is but this hair in a manner of enumerating Bright protection scope is not limited thereto.
The method for preparing xylitol with oil tea shell of the present embodiment, preparation process are as follows:
(1), sorting: selection nothing is rotted, without mildew, no disease and pests harm, fresh oil tea shell, spare;
(2), impregnate: oil tea shell being put into 4 times of weight, volumetric concentration to be soaked in 80% edible ethanol at normal temperatures and pressures 18h is steeped, soak is filtered off, 3 times of weight is added, the edible ethanol that volumetric concentration is 45%, 40min, mistake is impregnated at 50 DEG C Filter collects and impregnates oil tea shell, spare;
(3), dry: oil tea shell will be impregnated and be transferred in baking oven, dried to water content under 68 DEG C, normal pressure less than 8%, Oil tea shell must be dried, it is spare;
(4), crush: and then dry oil tea shell is ground into the oil tea shell particle of 15 mesh, it is spare;
(5), ferment: being added into oil tea shell particle and account for its weight 30%, the water that temperature is 38 DEG C, while be added and accounting for crude oil Tea shell weight 12% is mixed by calcium sulfate, sorghum flour, cellulase, saccharomycete by the weight ratio of 0.3:5:0.2:1 Leavening is sealed by fermentation processing 2 days at 30 DEG C, becomes fermentation oil tea shell particle, spare;
(6), homogeneous: being processed into uniform fermentation oil tea shell material through homogenizer at normal temperature for fermentation oil tea shell particle, standby With;
(7), hydrolyze: being added and crude oil tea shell particle identical weight, weight concentration 2.2% into fermentation oil tea shell material Oxalic acid aqueous solution, stir evenly, and be heated to 125 DEG C by the heating rate of 8 DEG C/min, heat while stirring, stirring rate is Then 20r/min handles 3.5h in the case where pressure is 1.4MPa;Thereafter, when being naturally cooling to 75 DEG C, oil tea is collected in filtering respectively Shell hydrolyzate and oil tea shell slag, it is spare;
(8), digest: the buck that oil tea shell slag clear water or weight concentration are 1.0% being cleaned 3 times, is drained;It adds and accounts for The zytase of its weight 1.8%, 0.3% papain, 0.8% calcium sulfate, 0.6% magnesium phosphate, mix, 25 Encapsulation process 30h at DEG C;Then the warm water for accounting for 3 times of oil tea shell slag weight, 45 DEG C is added, handles 30min, oil tea is collected in filtering Shell slag digests Aqueous extracts, spare;
(9), decolourize: be added into oil tea shell hydrolyzate account for its weight 20%, by neutral active charcoal particle, neutral diatomite, The silica gel of 100 mesh prepares the decolorising agent mixed, the stir process at 75 DEG C, stirring speed by the weight ratio of 1:1.25:0.4 Rate is 55r/min, and when the light transmittance of oil tea shell hydrolyzate reaches 85% or more, oil tea shell decoloration hydrolyzate is collected in filtering, standby With;
(10), neutralize: being slowly added to the aqueous sodium carbonate that weight concentration is 8%, Bian Jia into oil tea shell decoloration hydrolyzate While stirring, when the pH value of oil tea shell decoloration hydrolyzate reaches 6.2, oil tea shell neutralizing hydrolysis liquid is obtained, it is spare;
(11), mix: oil tea shell slag being digested into Aqueous extracts and oil tea shell neutralizing hydrolysis liquid mixes, it is naturally quiet to put 6h after stirring evenly, Filtering, obtains oil tea shell mixed aqueous solution, spare;
(12), cross column: oil tea shell mixed aqueous solution is heated to 40 DEG C, cross strong-base anion-exchange resin, flow velocity while hot For 22L/h, collects anion exchange resin and cross column liquid;Then anion exchange resin is crossed into column liquid and crosses Subacidity cation exchange Resin, flow velocity 15L/h collect cation exchange resin and cross column liquid;Cation exchange resin is crossed into column liquid again and is heated to 55 DEG C, S-330 type macroporous absorbent resin is crossed, flow velocity 42L/h collects macroporous absorbent resin and crosses column liquid, spare;
(13), it is concentrated: macroporous absorbent resin is crossed in column liquid investment inspissator, in the item that temperature is 55 DEG C, pressure is 3KPa Under part, the 1/6 of concentration to original volume, concentrated column liquid is obtained, it is spare;
(14), freeze: concentrated column liquid is transferred in freezer, quiet at 2 DEG C to put 6h, supernatant liquid is collected in filtering;Again to It is slowly added to the edible ethanol that volumetric concentration is 90% or more in supernatant liquid, reaches the volumetric concentration of the ethyl alcohol in supernatant liquid It is then, quiet in freezer to put to no Precipitation, filtering to 55%, precipitating is collected, it is spare;
(15), hydrogenate: the clear water of precipitating equivalent weight is dissolved, while the hydrogenation catalyst for accounting for Sediment weight 4% is added (metallic nickel), stirs evenly;Then pressure is 8MPa, temperature is 135 DEG C, the rate that is passed through of hydrogen is 2.0m3It is handled under/h 70min, the xylitol liquid after must hydrogenating are spare;
(16), crystallize: xylitol liquid is transferred in freezer, while the edible ethanol for being 95% or more with volumetric concentration is adjusted Concentration of alcohol in xylitol liquid is 65% or more, then, quiet to put to no Precipitation, filtering, collects xylitol precipitating;So Afterwards, it by xylitol precipitating deionized water dissolving, filters, then through drying, crushing to get xylitol.
The method for preparing xylitol with oil tea shell of the invention is suitable for preparing xylitol with oil tea shell, it can also be used to use The agricultural crops such as corncob, bagasse prepare xylitol.

Claims (6)

1. a kind of method for preparing xylitol with oil tea shell, it is characterised in that preparation process is as follows:
(1), sorting: selection nothing is rotted, without mildew, no disease and pests harm, fresh oil tea shell, spare;
(2), impregnate: by oil tea shell be put into 2-5 times of weight, volumetric concentration be 75-85% edible ethanol in, at normal temperatures and pressures 8-20h is impregnated, soak is filtered off, 2-5 times of weight is added, the edible ethanol that volumetric concentration is 35-50%, at 45-55 DEG C 30-50min is impregnated, filtering collects and impregnates oil tea shell, spare;
(3), dry: oil tea shell will be impregnated and be transferred in baking oven, dry to water content under 65-70 DEG C, normal pressure less than 8%, obtain Dry oil tea shell, it is spare;
(4), crush: and then dry oil tea shell is ground into the oil tea shell particle of 5-20 mesh, it is spare;
(5), ferment: being added into oil tea shell particle and account for its weight 25-35%, the water that temperature is 35-40 DEG C, while be added and accounting for original The leavening of oil tea shell weight 8-15.5% is sealed by fermentation processing 1-3 days at 28-35 DEG C, becomes fermentation oil tea shell particle, standby With;
(6), homogeneous: being processed into uniform fermentation oil tea shell material through homogenizer at normal temperature for fermentation oil tea shell particle, spare;
(7), hydrolyze: being added and crude oil tea shell particle identical weight, weight concentration 1.5-3.0% into fermentation oil tea shell material Sour water, stir evenly, and be heated to 110-140 DEG C by the heating rate of 5-10 DEG C/min, heat while stirring, be then in pressure 2.5-4.0h is handled under 1.25-1.5MPa;Thereafter, when being naturally cooling to 70-80 DEG C, oil tea shell hydrolyzate is collected in filtering respectively It is spare with oil tea shell slag;
(8), digest: the buck that oil tea shell slag clear water or weight concentration are 0.5-1.5% being cleaned 2-3 times, is drained;It adds Account for the zytase of its weight 1.2-2.5%, the papain of 0.1-0.5%, the calcium sulfate of 0.5-1.2%, 0.2-1.0% Magnesium phosphate, mix, the encapsulation process 20-38h at 20-30 DEG C;Then it is added and accounts for 2-3 times of oil tea shell slag weight, 40-50 DEG C Warm water handles 20-40min, and filtering collects oil tea shell slag and digests Aqueous extracts, spare;
(9), decolourize: being added into oil tea shell hydrolyzate and account for the decolorising agent of its weight 15-25%, the stir process at 70-80 DEG C, Stirring rate is 50-60r/min, and when the light transmittance of oil tea shell hydrolyzate reaches 85% or more, the decoloration of oil tea shell is collected in filtering Hydrolyzate, it is spare;
(10), neutralize: being slowly added to the buck that weight concentration is 5-10% into oil tea shell decoloration hydrolyzate, side edged stirs, to oil When the pH value of tea shell decoloration hydrolyzate reaches 6.0-6.5, oil tea shell neutralizing hydrolysis liquid is obtained, it is spare;
(11), mix: oil tea shell slag being digested into Aqueous extracts and oil tea shell neutralizing hydrolysis liquid mixes, it is naturally quiet to put 4-8h, mistake after stirring evenly Filter, obtains oil tea shell mixed hydrolysis liquid, spare;
(12), cross column: oil tea shell mixed hydrolysis liquid is heated to 35-45 DEG C, cross anion exchange resin, flow velocity 15- while hot 28L/h collects anion exchange resin and crosses column liquid;Then anion exchange resin is crossed into column liquid and crosses cation exchange resin, flowed Speed is 10-20L/h, collects cation exchange resin and crosses column liquid;Cation exchange resin is crossed into column liquid again and is heated to 50-60 DEG C, S-330 type macroporous absorbent resin is crossed, flow velocity 35-50L/h collects macroporous absorbent resin and crosses column liquid, spare;
The anion exchange resin is strong-base anion-exchange resin, and the cation exchange resin is Subacidity cation Exchanger resin;
(13), it is concentrated: macroporous absorbent resin is crossed in column liquid investment inspissator, in the item that temperature is 50-60 DEG C, pressure is 1-5KPa Under part, the 1/8-1/5 of concentration to original volume obtains concentrated column liquid, spare;
(14), freeze: concentrated column liquid is transferred in freezer, quiet at 0-6 DEG C to put 5-8h, supernatant liquid is collected in filtering;Again to It is slowly added to the edible ethanol that volumetric concentration is 90% or more in supernatant liquid, reaches the volumetric concentration of the ethyl alcohol in supernatant liquid It is then, quiet in freezer to put to no Precipitation, filtering to 45-65%, precipitating is collected, it is spare;
(15), hydrogenate: the clear water of precipitating equivalent weight is dissolved, while the hydrogenation catalyst for accounting for Sediment weight 3-5% is added, stir It is even;Then pressure is 5-10MPa, temperature is 120-150 DEG C, the rate that is passed through of hydrogen is 1-2.5m360- is handled under/h 75min, the xylitol liquid after must hydrogenating are spare;
(16), crystallize: xylitol liquid is transferred in freezer, while the edible ethanol for being 95% or more with volumetric concentration adjusts xylose Concentration of alcohol in alcohol liquid is 65% or more, then, quiet to put to no Precipitation, filtering, collects xylitol precipitating;Then, will Xylitol precipitating deionized water dissolving, filtering, then through drying, crushing to get xylitol.
2. the method for preparing xylitol with oil tea shell according to claim 1, it is characterised in that: hair described in fermentation procedure Ferment agent is by calcium sulfate, sorghum flour, cellulase, saccharomycete by (0.2-0.35): the mixing of the weight ratio of (4-6): 0.2:1 and At.
3. the method for preparing xylitol with oil tea shell according to claim 1, it is characterised in that: acid described in hydrolyzing process Water is one of hydrochloric acid, sulfuric acid, oxalic acid or a variety of aqueous solutions, when to be two or more, the weight such as the ratio of each component is Part or other ratios.
4. the method for preparing xylitol with oil tea shell according to claim 1, it is characterised in that: in hydrolyzing process, Bian Jia Hot side stirring, stirring rate 15-25r/min.
5. the method for preparing xylitol with oil tea shell according to claim 1, it is characterised in that: taken off described in bleaching process Toner be by neutral active charcoal particle, neutral diatomite, 80-120 mesh silica gel by 1:(1-1.5): the weight of (0.3-0.45) Ratio preparation mixes.
6. the method for preparing xylitol with oil tea shell according to claim 1, it is characterised in that: alkali described in neutralization step Water is one of sodium hydroxide, calcium hydroxide, sodium carbonate or a variety of aqueous solutions, and when to be two or more, each component is matched Than for etc. parts by weight or other ratios.
CN201610698186.1A 2016-08-19 2016-08-19 A method of xylitol is prepared with oil tea shell Active CN106316784B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610698186.1A CN106316784B (en) 2016-08-19 2016-08-19 A method of xylitol is prepared with oil tea shell

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610698186.1A CN106316784B (en) 2016-08-19 2016-08-19 A method of xylitol is prepared with oil tea shell

Publications (2)

Publication Number Publication Date
CN106316784A CN106316784A (en) 2017-01-11
CN106316784B true CN106316784B (en) 2019-03-01

Family

ID=57741270

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610698186.1A Active CN106316784B (en) 2016-08-19 2016-08-19 A method of xylitol is prepared with oil tea shell

Country Status (1)

Country Link
CN (1) CN106316784B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109053375B (en) * 2018-07-30 2021-05-11 南京林业大学 Method for utilizing all components of oil-tea camellia shell raw material
CN110036827A (en) * 2019-03-31 2019-07-23 贵州省贵福菌业发展有限公司 A kind of oil tea shell breaking method

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101195838A (en) * 2008-01-04 2008-06-11 安徽丰原发酵技术工程研究有限公司 New purpose of corn core
CN101709309A (en) * 2009-12-22 2010-05-19 安徽丰原发酵技术工程研究有限公司 Method for combined fermentation of ethanol and xylitol
CN101823939A (en) * 2009-09-29 2010-09-08 山东福田药业有限公司 Novel process for preparing xylitol
CN103320477A (en) * 2013-07-01 2013-09-25 南京林业大学 Comprehensive utilization method of oil-tea camellia shells

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI109993B (en) * 1999-07-02 2002-11-15 Neste Chemicals Oy A process for preparing polyols

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101195838A (en) * 2008-01-04 2008-06-11 安徽丰原发酵技术工程研究有限公司 New purpose of corn core
CN101823939A (en) * 2009-09-29 2010-09-08 山东福田药业有限公司 Novel process for preparing xylitol
CN101709309A (en) * 2009-12-22 2010-05-19 安徽丰原发酵技术工程研究有限公司 Method for combined fermentation of ethanol and xylitol
CN103320477A (en) * 2013-07-01 2013-09-25 南京林业大学 Comprehensive utilization method of oil-tea camellia shells

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
油茶壳水解制木糖醇的研究;许强思;《生物质化学工程》;19831231(第12期);第455-458页

Also Published As

Publication number Publication date
CN106316784A (en) 2017-01-11

Similar Documents

Publication Publication Date Title
CN104223125B (en) A kind of method preparing potato residues dietary fiber
CN101255479B (en) Pre-treatment method for highly-effective saccharification of lignocellulose
CN101643795B (en) Method for preparing xylose and xylitol by using bamboo
CN102517403B (en) Method for preparing hemicellulose oligosaccharide by high-temperature liquid water
CN105886577B (en) A kind of production method preparing high maltose syrup and dietary fiber using sweet potato starch processing waste residue
CN103013936A (en) Method for extracting anthocyanidin by using compound enzyme, and compound enzyme preparation thereof
CN100507009C (en) Process for producing oligofructose of garlic
CN102199225B (en) Method for preparing agrocybe cylindracea hydrolysate by using compound enzyme method
CN104774887A (en) Preparation method of corncob xylooligosaccharide
CN106316784B (en) A method of xylitol is prepared with oil tea shell
CN106912964A (en) Soluble dietary fiber and preparation method thereof
CN103131802A (en) Process for producing xylose by lignocellulose biomass
CN103397554A (en) New process for preparing microcrystalline cellulose from lignocelluloses biomass
CN104031172A (en) Method for extracting pectin from banana peel by ultrasonic synergistic ammonium oxalate method
CN103243138A (en) Method for preparing corncob xylooligosaccharide by a complex enzyme method
CN106086110B (en) A method of superhigh maltose syrup is prepared using sweet potato waste residue
CN102925516A (en) Xylo-oligosaccharide preparation method
CN105624235A (en) Method for preparing xylose by utilizing eucalyptus pulp waste liquid
CN115260334B (en) Compound extraction process of mulberry leaf polysaccharide
CN104762333B (en) The method that xylitol is prepared using winter bamboo shoot shell
CN106947000A (en) A kind of preparation method of high-purity polyfructosan
CN101979640B (en) Method for producing xylooligosaccharide by using sugarcane leaves
CN106282268B (en) A method of high maltose syrup is prepared by cadmium rice
CN105838757B (en) A kind of production method preparing isomalto-oligosaccharide using sweet potato waste residue
CN106399425A (en) Method using activated carbon absorption and ethanol desorption to synchronously produce different-quality xylooligosaccharide

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20230118

Address after: Room 704, Building 17, Meiyu Apartment, No. 398, Xinyao North Road, Tianxin District, Changsha City, Hunan Province, 410000

Patentee after: Hunan Yougu Hi Tech Co.,Ltd.

Address before: 410007 Yuguang District, Changsha, Hunan, 298 Shuguang Road No. 3 Tianyi city 3

Patentee before: Guan Tianqiu