CN101985579B - Method for decoloring fatty acid physically refined from rice bran oil - Google Patents

Method for decoloring fatty acid physically refined from rice bran oil Download PDF

Info

Publication number
CN101985579B
CN101985579B CN2010105426888A CN201010542688A CN101985579B CN 101985579 B CN101985579 B CN 101985579B CN 2010105426888 A CN2010105426888 A CN 2010105426888A CN 201010542688 A CN201010542688 A CN 201010542688A CN 101985579 B CN101985579 B CN 101985579B
Authority
CN
China
Prior art keywords
controlled
fatty acid
concentration
rice bran
acid
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
CN2010105426888A
Other languages
Chinese (zh)
Other versions
CN101985579A (en
Inventor
钟民强
徐建彬
徐青云
殷小平
顾经东
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.)
Jiangsu Yonglin Chemical Oil Co Ltd
Original Assignee
Jiangsu Yonglin Chemical Oil Co Ltd
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 Jiangsu Yonglin Chemical Oil Co Ltd filed Critical Jiangsu Yonglin Chemical Oil Co Ltd
Priority to CN2010105426888A priority Critical patent/CN101985579B/en
Publication of CN101985579A publication Critical patent/CN101985579A/en
Application granted granted Critical
Publication of CN101985579B publication Critical patent/CN101985579B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Fats And Perfumes (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

The invention provides a method for decoloring fatty acid physically refined from rice bran oil. By a method for adding a proper amount of decoloring agent into a mixed fatty acid system and redistilling, the defect of incapability of removing pink color of the rice bran oil-mixed fatty acid of the conventional redistillation technology is overcome, and the rice bran oil-mixed fatty acid has a yellowish color. Therefore, the application range of the rice bran oil-mixed fatty acid is widened. The method comprises the following steps of: 1, adding the following components into the rice bran oil-mixed fatty acid in percentage by weight: 0.01 to 0.1 percent of sulfuric acid at the concentration of 98 percent, 0.01 to 0.1 percent of phosphoric acid at the concentration of 85 percent, 0.05 to 0.25 percent of activated carbon and 0.01 to 0.5 percent of lithium carbonate; and 2, distilling under vacuum.

Description

A kind of method of Rice pollard oil physical refining lipid acid decolouring
Technical field
The present invention relates to a kind of method of Rice pollard oil physical refining lipid acid decolouring.Belong to the oil chemistry industrial circle.
Background technology
Rice pollard oil physical refining lipid acid often has pink color and luster, and employing generally steaming means again is difficult to remove pink color and luster, so not only influences the range of application of lipid acid, and has reduced the commodity value of lipid acid.In order to obtain the Rice pollard oil physical refining lipid acid of yellowish color and luster, we have drafted many ways and meanses, through the research and experiment of long period, have invented a kind of method of Rice pollard oil physical refining lipid acid decolouring finally.This method has not only solved the shortcoming that existing multiple steaming technique can not remove the pink color and luster of Rice pollard oil mixed fatty acid, makes the Rice pollard oil mixed fatty acid become the state of yellowish color and luster, has widened the range of application of Rice pollard oil mixed fatty acid.And have low cost, and processing ease, the product yield is high, the characteristics of constant product quality.
Summary of the invention
The problem that the present invention will solve is the shortcoming that existing multiple steaming technique can not remove the pink color and luster of Rice pollard oil mixed fatty acid, and in order to solve the problems of the technologies described above, the present invention adopts following technical scheme, and this method may further comprise the steps:
1, in the Rice pollard oil mixed fatty acid, % by weight adds the sulfuric acid 0.01~0.1% of 98% concentration, adds the phosphoric acid 0.01~0.1% of 85% concentration, adds activated carbon 0.05~0.25%, adds Quilonum Retard 0.01~0.5%.
Generally be controlled at 0.01~0.1% 1.1 add the sulfuric acid of 98% concentration, preferentially be controlled at 0.01~0.05%, especially 0.01~0.03%;
Generally be controlled at 0.01~0.1% 1.2 add the phosphoric acid of 85% concentration, preferentially be controlled at 0.01~0.06%, especially 0.015~0.035%;
Generally be controlled at 0.05~0.25% 1.3 add activated carbon, preferentially be controlled at 0.08~0.22%, especially 0.12~0.2%;
Generally be controlled at 0.01~0.5% 1.4 add Quilonum Retard, preferentially be controlled at 0.01~0.2%, especially 0.15~0.025%.
2, vacuum state distillation down.
2.1 vacuum tightness generally is controlled at 1~500Pa, preferentially is controlled at 50~300Pa, especially 100~200Pa;
2.2 the still kettle temperature generally is controlled at 200~250 ℃, preferentially is controlled at 210~240 ℃, especially 220~230 ℃;
Generally be controlled at 250~280 ℃ 2.3 distill whole temperature, preferentially be controlled at 255~275 ℃, especially 260~270 ℃.
Embodiment
Instance one
In flask, add Rice pollard oil physical refining lipid acid 1000g, the sulfuric acid 0.15g of 98% concentration, the phosphoric acid 0.2g of 85% concentration, activated carbon 1g, Quilonum Retard 0.2g, the glass pearl of boiling is an amount of.Load onto liquid thermometer and gas phase temperature meter, connect condensing surface and 2X type vacuum pump, open electrothermal heater, 2 ℃/min of control temperature rise rate; The open vacuum pump keeps vacuum residual voltage 100Pa, when 195 ℃ of liquidus temperatures, during 190 ℃ of gas phase temperatures; Beginning has overhead product, and a large amount of overhead products distillate for 200~230 ℃ in liquid phase, and a small amount of overhead product distillates for 230~270 ℃ in liquid phase; Collecting whole overhead products is 970g, obtains the lipid acid of yellowish color and luster, and pink color and luster originally is removed.
Instance two
In flask, add Rice pollard oil physical refining lipid acid 1000g, the sulfuric acid 0.2g of 98% concentration, the phosphoric acid 0.2g of 85% concentration, activated carbon 1.5g, Quilonum Retard 0.2g, the glass pearl of boiling is an amount of.Load onto liquid thermometer and gas phase temperature meter, connect condensing surface and 2X type vacuum pump, open electrothermal heater, 2 ℃/min of control temperature rise rate; The open vacuum pump keeps vacuum residual voltage 100Pa, when 195 ℃ of liquidus temperatures, during 190 ℃ of gas phase temperatures; Beginning has overhead product, and a large amount of overhead products distillate for 200~230 ℃ in liquid phase, and a small amount of overhead product distillates for 230~270 ℃ in liquid phase; Collecting whole overhead products is 973g, obtains the lipid acid of yellowish color and luster, and pink color and luster originally is removed.
Instance three
In flask, add Rice pollard oil physical refining lipid acid 1000g, the sulfuric acid 0.25g of 98% concentration, the phosphoric acid 0.2g of 85% concentration, activated carbon 2g, Quilonum Retard 0.2g, the glass pearl of boiling is an amount of.Load onto liquid thermometer and gas phase temperature meter, connect condensing surface and 2X type vacuum pump, open electrothermal heater, 2 ℃/min of control temperature rise rate; The open vacuum pump keeps vacuum residual voltage 100Pa, when 195 ℃ of liquidus temperatures, during 190 ℃ of gas phase temperatures; Beginning has overhead product, and a large amount of overhead products distillate for 200~230 ℃ in liquid phase, and a small amount of overhead product distillates for 230~270 ℃ in liquid phase; Collecting whole overhead products is 967g, obtains the lipid acid of yellowish color and luster, and pink color and luster originally is removed.
Instance four
In flask, add Rice pollard oil physical refining lipid acid 1000g, the sulfuric acid 0.2g of 98% concentration, the phosphoric acid 0.15g of 85% concentration, activated carbon 2g, Quilonum Retard 0.15g, the glass pearl of boiling is an amount of.Load onto liquid thermometer and gas phase temperature meter, connect condensing surface and 2X type vacuum pump, open electrothermal heater, 2 ℃/min of control temperature rise rate; The open vacuum pump keeps vacuum residual voltage 100Pa, when 195 ℃ of liquidus temperatures, during 190 ℃ of gas phase temperatures; Beginning has overhead product, and a large amount of overhead products distillate for 200~230 ℃ in liquid phase, and a small amount of overhead product distillates for 230~270 ℃ in liquid phase; Collecting whole overhead products is 965g, obtains the lipid acid of yellowish color and luster, and pink color and luster originally is removed.
Instance five
In flask, add Rice pollard oil physical refining lipid acid 1000g, the sulfuric acid 0.2g of 98% concentration, the phosphoric acid 0.2g of 85% concentration, activated carbon 2g, Quilonum Retard 0.2g, the glass pearl of boiling is an amount of.Load onto liquid thermometer and gas phase temperature meter, connect condensing surface and 2X type vacuum pump, open electrothermal heater, 2 ℃/min of control temperature rise rate; The open vacuum pump keeps vacuum residual voltage 100Pa, when 195 ℃ of liquidus temperatures, during 190 ℃ of gas phase temperatures; Beginning has overhead product, and a large amount of overhead products distillate for 200~230 ℃ in liquid phase, and a small amount of overhead product distillates for 230~270 ℃ in liquid phase; Collecting whole overhead products is 975g, obtains the lipid acid of yellowish color and luster, and pink color and luster originally is removed.

Claims (6)

1. the method for Rice pollard oil physical refining lipid acid decolouring, this method comprises the steps:
(1) in the Rice pollard oil mixed fatty acid, by weight percentage, add the sulfuric acid 0.01~0.1% of 98% concentration, add the phosphoric acid 0.01~0.1% of 85% concentration, add activated carbon 0.05~0.25%, add Quilonum Retard 0.01~0.5%;
(2) vacuum state distillation down.
2. the method for a kind of Rice pollard oil physical refining lipid acid decolouring according to claim 1 is characterized in that: in the step 1, by weight percentage,
The sulfuric acid that adds 98% concentration is controlled at 0.01~0.05%;
The phosphoric acid that adds 85% concentration is controlled at 0.01~0.06%;
Add activated carbon and be controlled at 0.08~0.22%;
Add Quilonum Retard and be controlled at 0.01~0.2%.
3. the method for a kind of Rice pollard oil physical refining lipid acid decolouring according to claim 1 is characterized in that: in the step 1, by weight percentage,
The sulfuric acid that adds 98% concentration is controlled at 0.01~0.03%;
The phosphoric acid that adds 85% concentration is controlled at 0.015~0.035%;
Add activated carbon and be controlled at 0.12~0.2%;
Add Quilonum Retard and be controlled at 0.15~0.025%.
4. the method for a kind of Rice pollard oil physical refining lipid acid decolouring according to claim 1 is characterized in that: in the step 2,
Vacuum degree control is at 1~500Pa;
The still kettle temperature is controlled at 200~250 ℃;
Distill whole temperature control at 250~280 ℃.
5. the method for a kind of Rice pollard oil physical refining lipid acid decolouring according to claim 1 is characterized in that: in the step 2,
Vacuum degree control is at 50~300Pa;
The still kettle temperature is controlled at 210~240 ℃;
Distill whole temperature control at 255~275 ℃.
6. the method for a kind of Rice pollard oil physical refining lipid acid decolouring according to claim 1 is characterized in that: in the step 2,
Vacuum degree control is at 100~200Pa;
The still kettle temperature is controlled at 220~230 ℃;
Distill whole temperature control at 260~270 ℃.
CN2010105426888A 2010-11-15 2010-11-15 Method for decoloring fatty acid physically refined from rice bran oil Expired - Fee Related CN101985579B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2010105426888A CN101985579B (en) 2010-11-15 2010-11-15 Method for decoloring fatty acid physically refined from rice bran oil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2010105426888A CN101985579B (en) 2010-11-15 2010-11-15 Method for decoloring fatty acid physically refined from rice bran oil

Publications (2)

Publication Number Publication Date
CN101985579A CN101985579A (en) 2011-03-16
CN101985579B true CN101985579B (en) 2012-06-27

Family

ID=43709981

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2010105426888A Expired - Fee Related CN101985579B (en) 2010-11-15 2010-11-15 Method for decoloring fatty acid physically refined from rice bran oil

Country Status (1)

Country Link
CN (1) CN101985579B (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010078491A1 (en) * 2008-12-31 2010-07-08 Battelle Memorial Institute Pre-esterification of primary polyols to improve solubility in solvents used in polyol process
CN101781605A (en) * 2010-02-05 2010-07-21 万福生科(湖南)农业开发股份有限公司 Refining method of rice bran oil
CN101805666A (en) * 2010-04-02 2010-08-18 安徽省思润谷物油精炼有限公司 Process for extracting high-grade rice bran oil by physical method

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090005583A1 (en) * 2007-06-29 2009-01-01 Benecke Herman P Preparation of Propylene Glycol Fatty Acid Ester or Other Glycol or Polyol Fatty Acid Esters

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010078491A1 (en) * 2008-12-31 2010-07-08 Battelle Memorial Institute Pre-esterification of primary polyols to improve solubility in solvents used in polyol process
CN101781605A (en) * 2010-02-05 2010-07-21 万福生科(湖南)农业开发股份有限公司 Refining method of rice bran oil
CN101805666A (en) * 2010-04-02 2010-08-18 安徽省思润谷物油精炼有限公司 Process for extracting high-grade rice bran oil by physical method

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
刘军海.米糠油精炼工艺研究新进展.《粮油加工》.2008,(第07期), *
李文波等.米糠油精炼工艺及开发应用前景.《粮食科技与经济》.2009,(第05期), *

Also Published As

Publication number Publication date
CN101985579A (en) 2011-03-16

Similar Documents

Publication Publication Date Title
EP2598228B1 (en) Methods and systems for solvent purification
CN102197121A (en) Palm oil, deodorized distillates and manufacturing methods therefor
Akgün Separation of squalene from olive oil deodorizer distillate using supercritical fluids
Wu et al. Optimization of deacidification of low-calorie cocoa butter by molecular distillation
CN101985579B (en) Method for decoloring fatty acid physically refined from rice bran oil
Chiavaro et al. Correlation between thermal properties and chemical composition of Italian virgin olive oils
Meyer et al. Application of short path distillation for recovery of polyphenols from deodorizer distillate
CN103342626A (en) Preparation method of chromatographic grade methanol
Chiavaro et al. Microwave heating of different commercial categories of olive oil: Part II. Effect on thermal properties
CN102827632B (en) Method for processing C5 raffinate from ethene cracking
CN104086412A (en) Process method for producing butyl oleate by using rape oil fatty acid
CN102850370A (en) Method for recovering 1,8-eucalyptol from eucalyptus oil by product
CN103288584B (en) Reformed arene C 10the processing method of middle extraction high-purity beta-methylnaphthalene
CN113652298A (en) Automatic primary refining method and system for butter raw fat in closed technological process of seasonings
CN202015515U (en) Extractive distillation equipment for crude benzol hydrofining
CN105349252A (en) Method for separating high-purity rice bran crude oil from rice bran
CN103044385A (en) Method for extracting thiophene in coking benzene with ionic liquid
Scheuren et al. Thermodynamic validation of wort boiling systems
Lu et al. Optimal start-up strategies for a conventional distillation column using simulated annealing
Petrozziello et al. Effect of the extent of ethanol removal on the volatile compounds of a Chardonnay wine dealcoholized by vacuum distillation
CN203303680U (en) Crude benzene refining, extracting and distilling device
Boudebouz et al. Processing factors that affect the balance of alcohols and alkyl esters during ‘Arbequina’olive oil production: Separation and clarification steps
CN101503411B (en) Method for separating sesamine from gingelly oil
CN203525358U (en) Device for extracting high-purity borneolum luodian
CN204058420U (en) A kind of grade rice bran oil preparation system

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
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20120627

Termination date: 20121115