CN105694527B - A kind of industrialized preparing process of lycopene oleoresin - Google Patents
A kind of industrialized preparing process of lycopene oleoresin Download PDFInfo
- Publication number
- CN105694527B CN105694527B CN201511011443.1A CN201511011443A CN105694527B CN 105694527 B CN105694527 B CN 105694527B CN 201511011443 A CN201511011443 A CN 201511011443A CN 105694527 B CN105694527 B CN 105694527B
- Authority
- CN
- China
- Prior art keywords
- tomato
- lycopene
- lycopene oleoresin
- preparing process
- skin
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B61/00—Dyes of natural origin prepared from natural sources, e.g. vegetable sources
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/10—Purification; Separation; Use of additives by extraction, i.e. purification or separation of liquid hydrocarbons with the aid of liquids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Water Supply & Treatment (AREA)
- Cosmetics (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
The present invention relates to a kind of industrialized preparing process of lycopene oleoresin, comprise the following steps:(1)Pretreatment of raw material:Tomato peel is dried by air flow dryer, Tomato Seed and skin are separated, tomato skin obtains tomato meal by fluidized bed drying, milling;(2)Extract:During tomato meal is added into alkanes and low molecule ketone mixed solvent, under water bath condition, stirring is extracted;(3)Concentration:Extract solution is evaporated under reduced pressure concentration under vacuum, recycling design obtains final product lycopene oleoresin.The present invention prepares tomato meal with tomato peel as raw material using the method for high temperature flash baking, and chroma loss is few.Mixed solvent is extracted and adapts to moisture material high, and extraction yield is high, and low cost is more suitable for continuous mass production, remarkable in economical benefits.
Description
Technical field
The invention belongs to natural extract technical field, and in particular to a kind of industrialized production side of lycopene oleoresin
Method.
Background technology
Lycopene is obtained from ripe tomato earliest, is one of stronger antioxidant.Its obvious health-care efficacy, resists
Oxidability is better than other carotenoid, is a kind of excellent natural.Lycopene has multiple biological activities,
It is the major carotenoids existed in human body.In recent years, lycopene was found have aobvious for preventing and improving prostatic disorders
Curative effect is write, is that health-product market is tried to be the first the gold product pursued at home and abroad.
The extracting method of current lycopene is a lot, but because raw material is in drying course, lycopene can be oxidized,
Loss is more, causes the lycopene rate of recovery not high.For example in Publication No. CN1364832A patents, with moisture 5~
The tomato meal of 10% (quality) is raw material, using the method for supercritical carbon dioxide extracting, and adds the mixing of ethanol and acetone
Solvent is to guide and support agent;Extracted in the state of being 5~30 kgs/hr in supercritical fluid carbon dioxide flow.Extracting yield is
80~90%.The method is relatively costly, the moisture obtained from drying, and lycopene is oxidized more.The method is dried
Operation chroma loss is big, and extraction yield is not high.In the patent of Publication No. CN102267855A, with tomato skin as raw material, warp
Solvent extraction, filtering, concentration, dry lycopene, wherein require that the tomato skin water content after dehydration is 6-10%, it is dried
Lycopene loss is more in journey, and its yield is difficult to ensure that production efficiency is also well imagined.And for example Publication No.
CN102516011A, with tomato as raw material, freeze-drying and dehydrating treatment, moisture requirement is less than 10%, and Extraction solvent is for acetone and just
Hexane, method is extracted for low-temperature ultrahigh-pressure cell instrument wall breaking technology secondary organic solvent.The lycopene that the method is prepared is brilliant
Body purity is higher, and because this method requirement moisture is relatively low, lycopene equally loses more.Therefore lycopene total yield
Relatively low, the another method need to use condition of ultralow temperature, and production cost is higher, is unsuitable for continuous mass production.
Learnt from current domestic literature, in Extracting of Lycopene, be required to the moisture of raw material less than 15%, or even
Require that moisture content of raw material is more low better in some patents, but when raw material dehydration is to less than 15%, lycopene content can be fast
Fast oxidational losses, chroma loss is up to 30%, causes overall recovery low, if raw material moisture is too high, conventional weak polar solvent recovery rate
It is low.Therefore, exploitation one kind can reduce lycopene and be lost in drying course, and from moisture raw tomatoes material higher
The method for extracting lycopene is extremely important, and drying course is tried one's best and reduces the loss of lycopene, improves production yield, reduces life
Produce cost, more conducively industrial continuous big production.
The content of the invention
In order to solve the difficult point of prior art, chroma loss of the lycopene in drying course is reduced, raising is extracted
Rate.The present invention provides a kind of method of industrialized production lycopene oleoresin.The method lycopene in drying course
Chroma loss is few, and lycopene extracts yield and overall recovery is higher.
The present invention solves the scheme taken of the technical problem:Comprise the following steps:
(1)Pretreatment of raw material:Tomato peel is dried by air flow dryer, Tomato Seed and skin are separated, and tomato skin is passed through
Fluidized bed drying, milling, obtains tomato meal;
(2)Extract:During tomato meal is added into alkanes and low molecule ketone mixed solvent, under water bath condition, stirring is carried
Take;
(3)Concentration:Extract solution is evaporated under reduced pressure concentration under vacuum, recycling design obtains final product lycopene oleoresin.
Step of the present invention(1)Middle air flow dryer, EAT is 200-400 DEG C, and leaving air temp is 60-90 DEG C,
Drying time is 10-60s, and tomato skin moisture is 35-45% after treatment.
Step of the present invention(1)Fluidized bed drying temperature is 40-50 DEG C, and the time is 40-100s.
Step of the present invention(1)Milling operation is whole to be blown using cold wind, obtains tomato meal moisture for 15-28%.
Step of the present invention(2)Alkane solvents are n-hexane, and low molecule ketones solvent is any in butanone, acetone
It is a kind of.
Step of the present invention(2)Ketones solvent volume parts are 15-24 parts, and alkane solvents volume parts are 85-76
Part.
Step of the present invention(2)Middle extraction bath temperature is 40-50 DEG C.
Step of the present invention(2)The ratio of tomato meal quality and solvent volume is 1 in abstraction process:3-7, the quality
Unit is kg, and the volume unit is L.
Step of the present invention(2)Extraction time is 2-4 times, and 2-4h is extracted every time, and each extract solution is merged.
Lycopene of the present invention and lycopene oleoresin colour value detection method normative reference《GB28316-2012 food
Safe national standard food additives tomato red》.
The computing formula of colour value extraction yield is in abstraction process of the present invention:
In formula:Y (%)-colour value extracts yield;The colour value of tomato meal after E1-drying;The color of E2-lycopene oleoresin
Valency;The quality of tomato meal, kg after M1-drying;The quality of M2-lycopene oleoresin, kg.
The computing formula of lycopene total recovery is in the present invention:
In formula:The total recovery of Y (%)-lycopene;The colour value of tomato peel before E0-drying;E2-lycopene oil tree
The colour value of fat;The quality of tomato peel, kg before M0-drying;The quality of M2-lycopene oleoresin, kg.
Using having the beneficial effect that above-mentioned technical proposal is produced:1st, raw material is ground using the method for high temperature flash baking treatment
Powder operation is blown using cold wind, reduces the oxidized speed of lycopene, and chroma loss is few, and the step colour value yield is more than 95%;
2nd, extracted using two kinds of larger double solvents of polarity spectrum.Polar solvent is using low molecule ketones solvent rather than low mass molecule alcohol
Class or esters, advantage are that ketones solvent dissolves each other effect more preferably with alkane solvents, and are not in molten using alcohols or esters
Agent mixes extraction wet stock layering with alkane solvents, causes to extract halfway phenomenon.The inventive method using n-hexane with
Low molecule ketones solvent compound collecting, can extract the small lycopene of polarity, and moisture material higher is adapted to again,
Yield more than 99% is extracted, lycopene overall recovery is up to 92%.No waste discharge, low cost, it is easy to accomplish continuous chemical industry
Industry is produced, remarkable in economical benefits.
Specific embodiment
With reference to specific embodiment, the present invention is further detailed explanation.
Embodiment 1
Tomato pomace 50kg is taken, colour value is 0.56.Dried by air flow dryer, EAT is 200 DEG C, leaving air temp is
60 DEG C, time 10s, moisture content of material is 45%.Seed and skin are separated, and by fluidized bed drying, temperature is 50 DEG C to tomato skin, when
Between 100s, milling, cold wind blows, and obtains tomato meal, and moisture is 28%, obtains tomato meal 9.5kg, colour value 2.9, colour value yield
It is 98.4%.
The tomato meal that will be obtained is added to 7 times of mixed solvents(Butanone:N-hexane=24:76)In, in 50 DEG C of water bath conditions
Under, stirring is extracted 4 times, and 2h is extracted every time.Each extract solution is merged, is -0.09MPa in vacuum, temperature is 45 DEG C of bar
Concentration is evaporated under reduced pressure under part, recycling design obtains final product lycopene oleoresin 329g, and colour value is 83.2.Colour value extracts yield
99.4%, lycopene total recovery is 97.8%.
Embodiment 2
Tomato pomace 100kg is taken, colour value is 0.63.Dried by air flow dryer, EAT is 400 DEG C, leaving air temp
It it is 90 DEG C, time 20s, moisture content of material is 35%.Seed and skin are separated, and by fluidized bed drying, temperature is 50 DEG C to tomato skin,
Time 40s, milling, cold wind blows, and obtains tomato meal, and moisture is 15.0%.Tomato skin powder 14.7kg is obtained, colour value is 4.1,
Colour value yield is 95.7%.
The tomato meal that will be obtained is added to 3 times of mixed solvents(Acetone:N-hexane=15:85)In, in 40 DEG C of water bath conditions
Under, stirring is extracted 4 times, and 3h is extracted every time.Each extract solution is merged, is -0.09MPa in vacuum, temperature is 45 DEG C of bar
Concentration is evaporated under reduced pressure under part, recycling design obtains final product lycopene oleoresin 700g, colour value 85.7.Colour value extracts yield
99.5%, lycopene total recovery is 95.2%.
Embodiment 3
Tomato pomace 50kg is taken, colour value is 0.50.Dried by air flow dryer, EAT is 300 DEG C, leaving air temp is
75 DEG C, time 30s, moisture content of material is 40%.Seed and skin are separated, and by fluidized bed drying, temperature is 45 DEG C to tomato skin, when
Between 70s, milling, cold wind blows, and obtains tomato meal, and moisture is 21.4%, obtains tomato meal 8.5kg, colour value 2.9, colour value yield
It is 98.6%.
The tomato meal that will be obtained is added to 5 times of mixed solvents(Butanone:N-hexane=19:81)In, under 45 DEG C of water bath conditions
Stirring is extracted 2 times, and 2.5h is extracted every time.Each extract solution is merged, is -0.09MPa in vacuum, temperature is 45 DEG C of condition
Lower that concentration is evaporated under reduced pressure, recycling design obtains final product lycopene oleoresin 294g, and colour value is 83.2.Colour value extracts yield
99.2%, lycopene total recovery is 97.8%.
Embodiment 4
Tomato pomace 100kg is taken, colour value is 0.60.Dried by air flow dryer, EAT is 350 DEG C, leaving air temp
It it is 80 DEG C, time 20s, moisture content of material is 35%.Seed and skin are separated, and by fluidized bed drying, temperature is 45 DEG C to tomato skin,
Time 80s, milling, cold wind blows, and obtains tomato meal, and moisture is 15.9%.Tomato skin powder 13.6kg is obtained, colour value is 4.2,
Colour value yield is 95.2%.
The tomato meal that will be obtained is added to 4 times of mixed solvents(Acetone:N-hexane=16:84)In, under 45 DEG C of water bath conditions
Stirring is extracted 3 times, and 3.5h is extracted every time.Each extract solution is merged, is -0.09MPa in vacuum, temperature is 45 DEG C of condition
Lower that concentration is evaporated under reduced pressure, recycling design obtains final product lycopene oleoresin 668g, colour value 85.4.It is 99.9% that colour value extracts yield,
Lycopene total recovery is 95.1%.
Embodiment 5
Tomato pomace 100kg is taken, colour value is 0.65.Dried by air flow dryer, EAT is 250 DEG C, leaving air temp
It it is 65 DEG C, time 60s, moisture content of material is 38%.Seed and skin are separated, and by fluidized bed drying, temperature is 40 DEG C to tomato skin,
Time 90s, milling, cold wind blows, and obtains tomato meal, and moisture is 22%.Tomato skin powder 12.2kg is obtained, colour value is 5.1, color
Valency yield is 95.7%.
The tomato meal that will be obtained is added to 4 times of mixed solvents(Butanone:N-hexane=20:80)In, under 46 DEG C of water bath conditions
Stirring is extracted 2 times, and 4h is extracted every time.Each extract solution is merged, is -0.09MPa in vacuum, temperature is under conditions of 45 DEG C
Concentration is evaporated under reduced pressure, recycling design obtains final product lycopene oleoresin 680g, colour value 91.2.It is 99.7% that colour value extracts yield, kind
Lycopene total recovery is 95.4%.
Preferred embodiment of the invention described in detail above.It should be appreciated that one of ordinary skill in the art without
Need creative work just can make many modifications and variations with design of the invention.Therefore, all technologies in the art
Personnel are available by logical analysis, reasoning, or a limited experiment on the basis of existing technology under this invention's idea
Technical scheme, all should be in the protection domain being defined in the patent claims.
Claims (6)
1. a kind of industrialized preparing process of lycopene oleoresin, it is characterised in that:Comprise the following steps:
(1)Pretreatment of raw material:Tomato peel is dried by air flow dryer, Tomato Seed and skin are separated, and tomato skin is by fluidisation
Bed is dried, milling, obtains tomato meal;The EAT of the air flow dryer is 200-400 DEG C, and leaving air temp is 60-90 DEG C,
Drying time is 10-60s, and tomato skin moisture is 35-45% after treatment;The drying temperature of the fluid bed is 40-50 DEG C,
Time is 40-100s;The milling operation is whole to be blown using cold wind, obtains tomato meal moisture for 15-28%;
(2)Extract:During tomato meal is added into alkanes and low molecule ketone mixed solvent, under water bath condition, stirring is extracted;
(3)Concentration:Extract solution is evaporated under reduced pressure concentration under vacuum, recycling design obtains final product lycopene oleoresin.
2. the industrialized preparing process of a kind of lycopene oleoresin according to claim 1, it is characterised in that:The step
Suddenly(2)Alkane solvents are n-hexane, and low molecule ketones solvent is any one in butanone, acetone.
3. the industrialized preparing process of a kind of lycopene oleoresin according to claim 1, it is characterised in that:The step
Suddenly(2)Ketones solvent volume parts are 15-24 parts, and alkane solvents volume parts are 85-76 parts.
4. the industrialized preparing process of a kind of lycopene oleoresin according to claim 1, it is characterised in that:The step
Suddenly(2)Middle extraction bath temperature is 40-50 DEG C.
5. the industrialized preparing process of a kind of lycopene oleoresin according to claim 1, it is characterised in that:The step
Suddenly(2)The ratio of tomato meal quality and solvent volume is 1 in abstraction process:3-7, the mass unit is kg, the volume list
Position is L.
6. the industrialized preparing process of a kind of lycopene oleoresin according to claim 1, it is characterised in that:The step
Suddenly(2)Extraction time is 2-4 times, and 2-4h is extracted every time, and each extract solution is merged.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201511011443.1A CN105694527B (en) | 2015-12-30 | 2015-12-30 | A kind of industrialized preparing process of lycopene oleoresin |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201511011443.1A CN105694527B (en) | 2015-12-30 | 2015-12-30 | A kind of industrialized preparing process of lycopene oleoresin |
Publications (2)
Publication Number | Publication Date |
---|---|
CN105694527A CN105694527A (en) | 2016-06-22 |
CN105694527B true CN105694527B (en) | 2017-05-31 |
Family
ID=56225904
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201511011443.1A Active CN105694527B (en) | 2015-12-30 | 2015-12-30 | A kind of industrialized preparing process of lycopene oleoresin |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN105694527B (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3702412A4 (en) * | 2017-10-25 | 2021-07-28 | Chenguang Biotech Group Co., Ltd. | Method for preparing lycopene crystals with high purity and low harm |
US11549128B2 (en) | 2017-10-25 | 2023-01-10 | Chenguang Biotech Group Co., Ltd. | Pretreatment method for producing lycopene raw material |
CN111943801A (en) * | 2019-05-17 | 2020-11-17 | 清馨(北京)科技有限公司 | Industrial production method of lycopene oleoresin |
CN111642727A (en) * | 2020-05-29 | 2020-09-11 | 江苏美鑫食品科技有限公司 | Tomato hotpot condiment with heat-clearing and detoxifying effects and preparation process thereof |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1328093A (en) * | 2001-07-27 | 2001-12-26 | 陶法 | Process for preparing lycopene |
CN101121631A (en) * | 2007-09-04 | 2008-02-13 | 江南大学 | Method for fast extracting lycopene |
CN101810225A (en) * | 2010-04-09 | 2010-08-25 | 新疆大学 | Method for producing lycopene oil resin and plant oil rich in lycopene |
CN102399120A (en) * | 2010-09-14 | 2012-04-04 | 乔振晴 | Method for extracting lycopene through supersonic saponification method |
-
2015
- 2015-12-30 CN CN201511011443.1A patent/CN105694527B/en active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1328093A (en) * | 2001-07-27 | 2001-12-26 | 陶法 | Process for preparing lycopene |
CN101121631A (en) * | 2007-09-04 | 2008-02-13 | 江南大学 | Method for fast extracting lycopene |
CN101810225A (en) * | 2010-04-09 | 2010-08-25 | 新疆大学 | Method for producing lycopene oil resin and plant oil rich in lycopene |
CN102399120A (en) * | 2010-09-14 | 2012-04-04 | 乔振晴 | Method for extracting lycopene through supersonic saponification method |
Also Published As
Publication number | Publication date |
---|---|
CN105694527A (en) | 2016-06-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN105694527B (en) | A kind of industrialized preparing process of lycopene oleoresin | |
CN103045356B (en) | Production method for linseed oil | |
CN101810225B (en) | Method for producing lycopene oil resin and plant oil rich in lycopene | |
CN103756782B (en) | Vegetable oil preparation method | |
CN101280121A (en) | Method for extracting corn flavochrome by microwave-ultrasonic | |
CN103936643A (en) | Method for extraction and separation of xanthophyll and flavones in marigold | |
CN106916624A (en) | A kind of idesia polycarpa oil CO 2 supercritical extracting method | |
CN103073914B (en) | Method for extracting maize yellow pigment from maize protein | |
CN105017055A (en) | Method for rapidly extracting and separating capsanthin and capsaicin from red chillies | |
CN106699625B (en) | The method that zeaxanthin is prepared from Chinese wolfberry fruit dregs | |
US11499052B2 (en) | Method for preparing lycopene crystals with high purity and low harm | |
CN105038962A (en) | Production process for rapeseed oil | |
CN108060012A (en) | A kind of extracting method of peony seed oil | |
CN104799240A (en) | Preparation method of micro-encapsulated scallion oil powder | |
CN103880804A (en) | Method for extracting and separating anthocyanin in purple potato powder | |
CN101704703A (en) | Method for producing high-purity lycopene powder by utilizing plant products | |
CN103420969A (en) | Method for extracting anthocyanidin in grape juice | |
CN103709021B (en) | Vanillin extraction method | |
CN101311148B (en) | Process for double-aqueous-phase extracting and refining persimmon lycopene | |
Nikolova et al. | Characteristics and functional properties of natural origin lycopene: a review | |
CN110108653B (en) | Method for analyzing capsorubin change rule in fresh pepper pretreatment process | |
CN107674452B (en) | Method for extracting Dan osmanthus yellow pigment | |
CN101732371B (en) | Co-production extract method of fruit oil and polysaccharide from seabuckthorn fruit paste | |
CN110527588B (en) | Subcritical extraction method of corn oil | |
CN103881808A (en) | Extraction method for tea seed oil |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
EE01 | Entry into force of recordation of patent licensing contract | ||
EE01 | Entry into force of recordation of patent licensing contract |
Application publication date: 20160622 Assignee: Xinjiang Chenxi Pepper Industry Co.,Ltd. Assignor: Chengguang Natural Pigment Group Co., Ltd. Contract record no.: 2019990000135 Denomination of invention: Industrial producing method of lycopene oil resin Granted publication date: 20170531 License type: Common License Record date: 20190430 |