KR970042599A - Manufacturing Method of High Substituted Positive Starch - Google Patents

Manufacturing Method of High Substituted Positive Starch Download PDF

Info

Publication number
KR970042599A
KR970042599A KR1019950065602A KR19950065602A KR970042599A KR 970042599 A KR970042599 A KR 970042599A KR 1019950065602 A KR1019950065602 A KR 1019950065602A KR 19950065602 A KR19950065602 A KR 19950065602A KR 970042599 A KR970042599 A KR 970042599A
Authority
KR
South Korea
Prior art keywords
starch
cationic
ammonium chloride
chloride
chloro
Prior art date
Application number
KR1019950065602A
Other languages
Korean (ko)
Other versions
KR100226154B1 (en
Inventor
장영상
김대현
정화영
유영수
Original Assignee
이삼우
주식회사 세원
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 이삼우, 주식회사 세원 filed Critical 이삼우
Priority to KR1019950065602A priority Critical patent/KR100226154B1/en
Publication of KR970042599A publication Critical patent/KR970042599A/en
Application granted granted Critical
Publication of KR100226154B1 publication Critical patent/KR100226154B1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B31/00Preparation of derivatives of starch
    • C08B31/16Ether-esters

Abstract

본 발명은 고치환도 양성전분의 제조방법에 관한 것으로 전분을 혼합기내에 투입하고 유동층 상태로 계속 혼합시키며 3-클로로-2-하이드록시프로필트리메틸암모늄 클로라이드(3-Chloro-2-hydrowypropylammonium chloride) 또는 에폭시프로필암모늄 클로라이드(Epoxypropy1-ammonium chloride)등의 양성화제를 미세하게 분무하는데, 이때 양성화제의 균일한 분무(噴霧)를 위하여 양성화제 액을 정량 압축펌프를 이용하여 2;1로 가압한 후 노즐을 통과시켜 비산하게 하여 전분가 접촉 면적을 최대한으로 하였다. 그리고 양성화 약품이 전분에 흡착하는 순간에 강력한 전단력을 가하여 덩어리(플록)가 생기는 것을 방지하였고(제2도)에서 보는 바와같이 이를 계속 와류(渦流)시켜 약품의 확산이 전분의 표면에서 내부로 침투되게끔하여 고치환도 양성전분의 제조방법을 제공한다. 본 발명에 의한 양성전분 제조법은 종래의 방법에 비해 반응수율이 높으며 치환도가 높을 뿐만 아니라 제조공정이 간단하여 공업적으로 매우 유용한 방법이다.The present invention relates to a method for producing a high-substituted cationic starch, the starch is added to the mixer and continuously mixed in a fluidized bed, 3-chloro-2-hydroxypropyltrimethylammonium chloride (3-Chloro-2-hydrowypropylammonium chloride) or epoxy Atomizers such as propyl ammonium chloride (Epoxypropy1-ammonium chloride) are finely sprayed. At this time, in order to uniformly spray the amphoterics, the anolyte solution is pressurized to 2: 1 using a quantitative compression pump. It was made to pass through, and the starch contact area was maximized. At the moment when the protonated chemical is adsorbed on the starch, strong shearing force is applied to prevent the formation of lumps (Flock). As shown in Fig. 2, the vortex is continuously vortexed so that the diffusion of the chemical penetrates from the surface of the starch. It provides a method of producing high-substituted cationic starch. Cationic starch production method according to the present invention is a highly useful method industrially because the reaction yield is higher than the conventional method, the degree of substitution is high, and the manufacturing process is simple.

Description

고치환도 양성 전분의 제조방법Manufacturing Method of High Substituted Positive Starch

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (7)

양성전분을 제조함에 있어서, 전분을 혼합기내에서 유동층상태로 혼합시키면서 양성화제를 분무하여 건조분말상태에서 치환도(D.S,; Degree of substitution) 0.02~0.50의 양성 전분을 제조함을 특징으로 하는 고치환도 양성전분의 제조방법.In preparing the cationic starch, the cationic agent is sprayed while mixing the starch in the fluidized bed state in the mixer to prepare a cationic starch having a degree of substitution (DS, 0.02 to 0.50) in the dry powder state. Method for preparing a degree of substitution cationic starch. 제1항에 있어서, 용매로써 물을 총량 대비 20%이하 사용하고, 촉매로서 산, 알카리를 사용함을 특징으로 하는 고치환도 양성전분의 제조방법.The method according to claim 1, wherein water is used in an amount of 20% or less relative to the total amount, and acid and alkali are used as catalysts. 제1항에 있어서 양성화제가 3-클로로-2-하이드록시프로필트리메틸암모늄 클로라이드(CIIPTMAC; 3-chloro-2-hydroxypropyltrimethylammonium chloride) 또는 에폭시프로필암모늄 클로라이드(Epoxypropyl-ammonium chloride)임을 특징으로 하는 고치환도 양성전분의 제조방법.The method of claim 1, wherein the protonating agent is high-substituted positive, characterized in that 3-chloro-2-hydroxypropyltrimethylammonium chloride (CIIPTMAC) or epoxypropyl-ammonium chloride (Epoxypropyl-ammonium chloride) Method of Making Starch. 제1항에 있어서 전분으로서, 옥수수전분, 밀전분, 감자전분, 타피오카전분,쌀전분등의 산업적 양산이 가능한 모든 전분을 사용함을 특징으로 하는 고치환도 양성전분의 제조방법.The method according to claim 1, wherein all starches capable of industrial mass production such as corn starch, wheat starch, potato starch, tapioca starch, rice starch and the like are used as starch. 제1항에 있어서 전분으로서,전분 자체의 개질(改質)을 위하여 포도당 분자내의 수산기(水酸基)를 치환하여 에테르(Ether),에스테르(Ester)형태로 된 유도전분(誘導澱粉)을 사용하거나 가교(架橋) 전분을 사용함을 특징으로 하는 고치환도 양성전분의 제조방법.The method according to claim 1, wherein as a starch, modified starch is used to replace hydroxyl groups in glucose molecules and use crosslinked derivatives of ether or ester to form starch or crosslink. A process for producing highly substituted cationic starches, characterized by the use of starch. 제1항에 있어서 전분으로서,전분을 CH2= CH-X의 형태의 고분자 단량체(여기에서 X는 소수성의 -CN,-CO2R중의 한 형태(예를들면, 아크릴로니트릴)이거나, -CO2II, -CONH2, -CO(CH2)n, -N+RC1- 중의 한형태(예를들면 아크릴산)중의 한가지를 사용하여 그라프팅한 전분을 사용함을 특징으로 하는 고치환도 양성전분의 제조방법.The starch of claim 1, wherein the starch is a polymer monomer in the form of CH 2 = CH—X, wherein X is one of hydrophobic —CN, —CO 2 R (eg acrylonitrile), or Highly substituted cationic starches characterized by using grafted starch using one of CO 2 II, -CONH 2 , -CO (CH 2 ) n and -N + RC 1- (eg acrylic acid). Manufacturing method. 제1항에 있어서, 혼합기(믹서)내의 주날개 스피드가 5-50 m/sec, 쵸파의 회전수가 1000-3000rpm, 반응온도 15℃-60℃로 함을 특징으로 하는 고치환도 양성전분의 제조방법.The preparation of the highly substituted cationic starch according to claim 1, wherein the main blade speed in the mixer is 5-50 m / sec, the rotation speed of the chopper is 1000-3000 rpm, and the reaction temperature is 15 ° C-60 ° C. Way.
KR1019950065602A 1995-12-29 1995-12-29 Method of preparing highly substituted cationic starch KR100226154B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1019950065602A KR100226154B1 (en) 1995-12-29 1995-12-29 Method of preparing highly substituted cationic starch

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1019950065602A KR100226154B1 (en) 1995-12-29 1995-12-29 Method of preparing highly substituted cationic starch

Publications (2)

Publication Number Publication Date
KR970042599A true KR970042599A (en) 1997-07-24
KR100226154B1 KR100226154B1 (en) 1999-10-15

Family

ID=19447090

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019950065602A KR100226154B1 (en) 1995-12-29 1995-12-29 Method of preparing highly substituted cationic starch

Country Status (1)

Country Link
KR (1) KR100226154B1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101467907B1 (en) * 2013-05-24 2014-12-02 경희대학교 산학협력단 Preparation method of cationic starch using ultra high pressure

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4464528A (en) * 1982-12-16 1984-08-07 The Dow Chemical Company Process for making cationic starch
DE3604796A1 (en) * 1986-02-15 1987-08-20 Degussa METHOD FOR DRYING THE STARCH

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101467907B1 (en) * 2013-05-24 2014-12-02 경희대학교 산학협력단 Preparation method of cationic starch using ultra high pressure

Also Published As

Publication number Publication date
KR100226154B1 (en) 1999-10-15

Similar Documents

Publication Publication Date Title
Varshney et al. Chemical functionalization of cellulose derived from nonconventional sources
Bukzem et al. Optimization of carboxymethyl chitosan synthesis using response surface methodology and desirability function
Prado et al. Cationization of polysaccharides: A path to greener derivatives with many industrial applications
Heinze et al. Carboxymethyl ethers of cellulose and starch–a review
US4129722A (en) Process for the preparation of high D. S. polysaccharides
CA2160542C (en) Method of making amide modified carboxyl-containing polysaccharide and fatty amide-modified polysaccharide so obtainable
EP2079762B1 (en) A process for the preparation of hydroxy polymer esters and their use
US4663448A (en) Aldehyde-containing heterpolysaccharides, a process for their preparation, and the use thereof
CN110799548A (en) Cellulose derivatives
EP2174959A1 (en) Etherified thinned starch
Bordenave et al. Advances on selective C-6 oxidation of chitosan by TEMPO
CN105622780B (en) A kind of homogeneous preparation method of quaternized chitin
JPS62192402A (en) Galactomannan dry cationization
EP1629016B1 (en) A process for the preparation of hydroxy polymer esters
US20060041117A1 (en) Process for the preparation of cellulose derivatives containing amino groups
JP6376365B2 (en) Stabilized size formulation
KR970042599A (en) Manufacturing Method of High Substituted Positive Starch
JP6376366B2 (en) Stabilized size formulation
KR100369517B1 (en) Method for preparing a low molecular weight polysaccharides and oligosaccharides
CN106674362A (en) Method for preparing paraphthaloyl chloride crosslinked starch by using ethanol solvent
JP3848992B2 (en) Base material for pulverization of liquid substances
US3705891A (en) Method for producing ungelatinized starch derivatives
KR100381387B1 (en) Manufacturing method of chitosan derivative
US20010025102A1 (en) Cold water soluble starch aldehydes and the method of preparation thereof
US2857377A (en) Amylaceous esters of sulfamic acid

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 20120716

Year of fee payment: 14

FPAY Annual fee payment

Payment date: 20130723

Year of fee payment: 15

LAPS Lapse due to unpaid annual fee