CN101747445B - Method for preparing hydroxypropul starch under ultrasound and microwave synergistic effect - Google Patents

Method for preparing hydroxypropul starch under ultrasound and microwave synergistic effect Download PDF

Info

Publication number
CN101747445B
CN101747445B CN 200810154106 CN200810154106A CN101747445B CN 101747445 B CN101747445 B CN 101747445B CN 200810154106 CN200810154106 CN 200810154106 CN 200810154106 A CN200810154106 A CN 200810154106A CN 101747445 B CN101747445 B CN 101747445B
Authority
CN
China
Prior art keywords
starch
microwave
percent
reaction
ultrasound
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.)
Expired - Fee Related
Application number
CN 200810154106
Other languages
Chinese (zh)
Other versions
CN101747445A (en
Inventor
胡爱军
吴聪
郑捷
秦志平
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.)
ZHEJIANG DIQIUCUN ENVIRONMENT PROTECTION TECHNOLOGY CO., LTD.
Original Assignee
Tianjin University of Science and Technology
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 Tianjin University of Science and Technology filed Critical Tianjin University of Science and Technology
Priority to CN 200810154106 priority Critical patent/CN101747445B/en
Publication of CN101747445A publication Critical patent/CN101747445A/en
Application granted granted Critical
Publication of CN101747445B publication Critical patent/CN101747445B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

The invention relates to a method for preparing hydroxypropul starch under ultrasound and microwave synergistic effect, belonging to the grain processing field; cereal grains or yam starch are used as raw material, epoxypropane is taken as etherifying agent, sodium hydroxide is taken as catalyst, and anhydrous sodium sulfate is used as swelling restraining agent, and the hydroxypropul starch is prepared under the ultrasound and microwave synergistic effect; the starch raw material is prepared into starch milk with 10-50 percent of concentration by mass ratio, and then the starch milk is placed in an ultrasonic wave reactor with 200W-800W of supersonic wave electric power and 20kHz-500kHz of frequency, ultrasound action is carried out for 10-60min, and then the starch milk is taken out, filtered and dried, and then the starch milk is mixed with 0.2-0.4 percent of sodium hydroxide, 1.0-3.0 percent of the anhydrous sodium sulfate and 2.0-7.2 percent of epoxypropane, the mixture is fully stirred and mixed uniformly, and then the mixture is placed in a microwave reactor for reaction, the microwave power is 60-300W, and the microwave action time is 2-20min; after the reaction is carried out, the reaction product is taken out and is neutralized by HCL with 1mol/L until the pH value is 5.5-6.0, and then the drying is carried out, so as to obtain the hydroxypropul starch with 0.01-2.00 of molecule substitution degree; in the method, the reaction time is short, the efficiency is high, the product quality is good, the molecule substitution degree can be adjusted in a large range, and the application range is wide.

Description

A kind of method for preparing hydroxypropylated starch through ultrasonic and microwave cooperating effect
Technical field
The invention belongs to the grain processing field.Relate in particular to a kind of method for preparing hydroxypropylated starch through ultrasonic and microwave cooperating effect.
Background technology
Hydroxypropylated starch is a kind of important chemically modified starch, after its modification, because etherification starch replaces the stability height of ehter bond; The hydroxypropyl possess hydrophilic property can weaken the inside HYDROGEN BOND INTENSITY of starch granules structure, makes it be easy to expand; Gelatinization is easy, and it is transparent to stick with paste liquid, good fluidity; A little less than the retrogradation property, stability is high.Hydroxypropyl corn starch all can be used in industries such as food, printing, weaving, printing and dyeing, washing composition, papermaking, medicine, metallurgy, petroleum drillings.In foodstuffs industry, can be used as thickening material, suspension agent and coating etc., be specially adapted to frozen product and ready-to-eat, make food when low-temperature storage, have good water-retentivity as thickening material.In paper industry, can be used as paper internal sizing and top sizing, make printing-ink distinct, even, reduce ink consumption.Can be used as warp size in textile industry, the wear resistance when raising is weaved etc.
The working method of hydroxypropylated starch has dry method, water dispersion and non-water dispersion.Dry process is that starch and propylene oxide directly carry out gas-solid reaction under certain condition.Concrete working method mainly contains alr mode, boiling mode and fashion of extrusion etc.The dry production reaction efficiency is low, and the molecule substitution value of products therefrom is low, heterogeneity, and the product separation purification difficult etc.Water dispersion is present widely used method, but also can not make the high substitution value product, and general molecule substitution value is not more than 0.3.Non-aqueous solvent method is with in starch dispersion and alcohol or the ketone organic solvent, and then with propylene oxide reaction, the sub-substitution value of the best result of products obtained therefrom is below 2.0.Generally speaking, all there is following problem in the various working methods of existing hydroxypropylated starch: reaction efficiency is low, and the molecule substitution value of gained hydroxypropylated starch is low, heterogeneity.
UW is a kind of mechanical wave of in elastic medium, propagating, and has heat effect, mechanical effect and cavitation effect.After UW acts on starch, can make the surface of starch granules form many small holes, the viscosity degradation of starch paste can quicken chemical reaction process.Microwave has inner heat characteristic, can make starch expanded, and chemical reaction is quickened.
Summary of the invention
With the propylene oxide is etherifying agent, and through supersonic method, microwave method synergy, synthetic hydroxypropyl corn starch is not seen any report so far as yet.The object of the invention is in order to solve low, the inhomogenous problem of reaction efficiency molecule substitution value low, the gained hydroxypropylated starch that the various working methods of hydroxypropylated starch all exist, for starch deep processing and application ultrasonic, microwave provide useful reference.
The present invention realizes through following method and technology scheme:
It is 10%~50% milk of starch that starch material (can use Cereals or potato starchs such as W-Gum, glutinous rice starch, wheat starch, green starch, yam starch, tapioca(flour)) is made into concentration by mass ratio; Placing hyperacoustic electric power is that 200W~800W, frequency are the ultrasound reactor of 20kHz~500kHz; Ultrasonication 10min~60min takes out suction filtration then; Oven dry; Again its catalyzer-sodium hydroxide 1.0%~3.0% repression of swelling agent-SODIUM SULPHATE ANHYDROUS 99PCT, 2.0%~7.2% propylene oxide with 0.2%~0.4% is mixed, fully stir, mix, be placed in the microwave reactor at last and react; The power of microwave is 60W-300W, and be 2min~20min action time.Reaction finishes, and the HCL that takes out with 1mol/L is neutralized to pH5.5-6.0, dries to get final product to such an extent that the molecule substitution value is 0.01~2.00 hydroxypropylated starch.
Compare with working method in the past; The invention has the advantages that: the reaction times is short, reaction efficiency is high, the product substitution value is adjustable in a big way, quality product stable homogeneous, performance are good, can use in many industries such as food, printing, weaving, printing and dyeing, washing composition, papermaking, medicine, metallurgy, petroleum drilling.
Embodiment
Below in conjunction with instance the present invention is described further.
Example one
It is 40% milk of starch that W-Gum is made into concentration by mass ratio, and placing hyperacoustic electric power is that 200W, frequency are the ultrasound reactor of 20kHz, ultrasonication 10min; Take out then, the suction filtration oven dry mixes its sodium hydroxide 2.8% SODIUM SULPHATE ANHYDROUS 99PCT, 3.4% propylene oxide with 0.32% again; Fully stir, mix; Be placed in the microwave reactor at last and react, the power of microwave is 100W, and be 2min action time.Reaction finishes, and the HCL that takes out with 1mol/L is neutralized to pH5.5~6.0, dries, and gets final product to such an extent that the molecule substitution value is 0.03 hydroxypropylated starch.
Example two
It is 45% milk of starch that the wheat starch raw material is made into concentration by mass ratio, and placing hyperacoustic electric power is that 250W, frequency are the ultrasound reactor of 40kHz, ultrasonication 30min; Take out then, the suction filtration oven dry mixes its sodium hydroxide, 3.0% SODIUM SULPHATE ANHYDROUS 99PCT, 3.8% propylene oxide with 0.35% again; Fully stir, mix; Be placed in the microwave reactor at last and react, the power of microwave is 150W, and be 3min action time.Reaction finishes, and the HCL that takes out with 1mol/L is neutralized to pH5.5~6.0, dries to get final product to such an extent that the molecule substitution value is 0.09 hydroxypropylated starch.
Example three
It is 42% milk of starch that the yam starch raw material is made into concentration by mass ratio, and placing hyperacoustic electric power is that 300W, frequency are the ultrasound reactor of 20kHz, ultrasonication 40min; Take out then, the suction filtration oven dry mixes it again with 0.38% sodium hydroxide, 3.0% SODIUM SULPHATE ANHYDROUS 99PCT, 3.9% propylene oxide; Fully stir, mix; Be placed in the microwave reactor at last and react, the power of microwave is 200W, and be 2min action time.Reaction finishes, and the HCL that takes out with 1mol/L is neutralized to pH5.5~6.0, dries to get final product to such an extent that the molecule substitution value is 1.50 hydroxypropylated starch.

Claims (2)

1. working method for preparing hydroxypropylated starch through ultrasonic and microwave cooperating effect; It is characterized in that: it is 10%~50% milk of starch that starch material is made into concentration by mass ratio, and placing hyperacoustic electric power is that 200W~800W, frequency are the ultrasound reactor of 20kHz~500kHz, ultrasonication 10min~60min; Take out then; Suction filtration, oven dry mixes its catalyzer-sodium hydroxide 1.0%~3.0% repression of swelling agent-SODIUM SULPHATE ANHYDROUS 99PCT, 2.0%~7.2% propylene oxide with 0.2%~0.4% again; Fully stir, mix; Be placed in the microwave reactor at last and react, the power of microwave is 60W-300W, and be 2min~20min action time; Reaction finishes, and the HCL that takes out with 1mol/L is neutralized to pH5.5-6.0, dries to get final product to such an extent that the molecule substitution value is 0.01~2.00 hydroxypropylated starch.
2. as claimed in claim 1ly a kind ofly prepare the method for hydroxypropylated starch through ultrasonic and microwave cooperating effect, it is characterized in that: described starch material is W-Gum, glutinous rice starch, wheat starch, green starch, yam starch, tapioca(flour).
CN 200810154106 2008-12-15 2008-12-15 Method for preparing hydroxypropul starch under ultrasound and microwave synergistic effect Expired - Fee Related CN101747445B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 200810154106 CN101747445B (en) 2008-12-15 2008-12-15 Method for preparing hydroxypropul starch under ultrasound and microwave synergistic effect

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 200810154106 CN101747445B (en) 2008-12-15 2008-12-15 Method for preparing hydroxypropul starch under ultrasound and microwave synergistic effect

Publications (2)

Publication Number Publication Date
CN101747445A CN101747445A (en) 2010-06-23
CN101747445B true CN101747445B (en) 2012-12-12

Family

ID=42475116

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 200810154106 Expired - Fee Related CN101747445B (en) 2008-12-15 2008-12-15 Method for preparing hydroxypropul starch under ultrasound and microwave synergistic effect

Country Status (1)

Country Link
CN (1) CN101747445B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102504035A (en) * 2011-11-02 2012-06-20 山东福洋生物科技有限公司 Method for increasing substitution degree of hydroxypropul starch
CN107244828B (en) * 2017-06-02 2018-08-28 安徽喜宝高分子材料有限公司 A kind of resistance to water-white lacquer
CN107352854A (en) * 2017-06-02 2017-11-17 安徽喜宝高分子材料有限公司 A kind of true mineral varnish with favorable elasticity

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996006866A1 (en) * 1994-08-31 1996-03-07 Rijksuniversiteit Te Groningen Method of modifying starch
EP1473308A1 (en) * 2003-04-28 2004-11-03 B. Braun Melsungen Ag Derivatives of starch for clinic use, especially parenteral
CN101280121A (en) * 2008-05-27 2008-10-08 曹龙奎 Method for extracting corn flavochrome by microwave-ultrasonic

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996006866A1 (en) * 1994-08-31 1996-03-07 Rijksuniversiteit Te Groningen Method of modifying starch
EP1473308A1 (en) * 2003-04-28 2004-11-03 B. Braun Melsungen Ag Derivatives of starch for clinic use, especially parenteral
CN101280121A (en) * 2008-05-27 2008-10-08 曹龙奎 Method for extracting corn flavochrome by microwave-ultrasonic

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
何小维等.物理场改性淀粉的研究.《食品工业科技》.2005,(第09期), *
周昆等.超声-微波协同水解玉米淀粉生成乙酰丙酸的工艺研究.《食品工业科技》.2008,(第02期), *

Also Published As

Publication number Publication date
CN101747445A (en) 2010-06-23

Similar Documents

Publication Publication Date Title
CN110590966B (en) Preparation method of modified starch ether for improving tile adhesive sliding property
CN101747445B (en) Method for preparing hydroxypropul starch under ultrasound and microwave synergistic effect
CN103773747A (en) Surface sizing special enzyme and preparation method thereof
CN101891829A (en) Acid hydrolysis modified starch and method for preparing same
CN1911966A (en) Pretreatment method of starch
CN109400728A (en) A kind of converted starch and preparation method thereof applied in jam production
CN110140863A (en) A kind of production method of water-milling glutinous rice flour
CN103833862B (en) A kind of oxidation glutinous rice starch and preparation method thereof and application
CN106046200A (en) Preparation method of carboxymethyl chitosan
CN101357970A (en) Carboxymethyl wood flour water absorbent and preparation method thereof
CN104497154A (en) Preparation method of hydroxy butyl starch ether or hydroxy butyl modified starch ether
CN103130901B (en) Octenyl succinic acid cannaedulisker starch ester and preparation method thereof
CN109251278A (en) A kind of preparation method of mushroom bran base high water-absorption resin
CN104497155A (en) Modified starch for environment-friendly starch-based wallpaper glue and preparation method of modified starch
CN103131350B (en) Cooked gelatine powder and preparation method thereof
CN105062392B (en) A kind of Lauxite flour composition and its preparation method and application
CN109485741A (en) A kind of preparation process of hydroxypropyl PASELLI EASYGEL
CN101423588A (en) Industrial synthesis method for producing high water absorption resin
CN106496653A (en) A kind of preparation method of hydroxypropul starch/sodium alginate composite membrane
CN102532328B (en) Starch Based Pigments and preparation method thereof, applies coating and the White Board of this Starch Based Pigments
CN105506026B (en) A kind of preparation method of irradiated biological complex denaturation coating starch
CN1281627C (en) Process for preparing pre-dextrinized hydropropyl di-starch phosphoric ester
CN101357971B (en) Organic solvent water absorbent and preparation method thereof
CN104211825B (en) Micro water solid phase modifying method of gleditsia sinensis polysaccharide gum
CN114891128A (en) Preparation and use method of modified starch inhibitor for hematite reverse flotation

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
ASS Succession or assignment of patent right

Owner name: ZHEJIANG DIQIUCUN ENVIRONMENTAL PROTECTION TECHNOL

Free format text: FORMER OWNER: TIANJIN UNIVERSITY OF SCIENCE + TECHNOLOGY

Effective date: 20150204

C41 Transfer of patent application or patent right or utility model
COR Change of bibliographic data

Free format text: CORRECT: ADDRESS; FROM: 300457 HANGU, TIANJIN TO: 310000 HANGZHOU, ZHEJIANG PROVINCE

TR01 Transfer of patent right

Effective date of registration: 20150204

Address after: 308 room 22, building 2, Huafeng Road, Xiacheng District, Hangzhou, Zhejiang, 310000

Patentee after: ZHEJIANG DIQIUCUN ENVIRONMENT PROTECTION TECHNOLOGY CO., LTD.

Address before: 300457 Tianjin economic and Technological Development Zone, No. thirteenth Main Street, No. 29

Patentee before: Tianjin University of Science & Technology

CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20121212

Termination date: 20181215