CN106046424A - Neo-welan gum blend modified pullulan-grafted pineapple fiber packaging film and preparation method thereof - Google Patents
Neo-welan gum blend modified pullulan-grafted pineapple fiber packaging film and preparation method thereof Download PDFInfo
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- CN106046424A CN106046424A CN201610518833.6A CN201610518833A CN106046424A CN 106046424 A CN106046424 A CN 106046424A CN 201610518833 A CN201610518833 A CN 201610518833A CN 106046424 A CN106046424 A CN 106046424A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/02—Cellulose; Modified cellulose
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D65/00—Wrappers or flexible covers; Packaging materials of special type or form
- B65D65/38—Packaging materials of special type or form
- B65D65/46—Applications of disintegrable, dissolvable or edible materials
- B65D65/466—Bio- or photodegradable packaging materials
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2301/00—Characterised by the use of cellulose, modified cellulose or cellulose derivatives
- C08J2301/02—Cellulose; Modified cellulose
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2405/00—Characterised by the use of polysaccharides or of their derivatives not provided for in groups C08J2401/00 or C08J2403/00
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/06—Biodegradable
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/16—Applications used for films
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W90/00—Enabling technologies or technologies with a potential or indirect contribution to greenhouse gas [GHG] emissions mitigation
- Y02W90/10—Bio-packaging, e.g. packing containers made from renewable resources or bio-plastics
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Abstract
The invention discloses a neo-welan gum blend modified pullulan-grafted pineapple fiber packaging film, comprising the following components according to parts by weight: 125-300 parts of pineapple leaf fiber, 6-6.5 parts of composite cellulase, 2.8-3 parts of nano magnesia particles, 4.4-4.5 parts of citric acid, 19-20 parts of neo-welan gum, 26-28 parts of pullulan, 4-5 parts of nano graphene, 4-5 parts of ethylene glycol, 9-10 parts of lentinan, 19-20 parts of coconut leaf cellulose, 5-6 parts of dimethyl silicone oil, 4-5 parts of propyl gallate, suitable water and suitable deionized water. The neo-welan gum blend modified pullulan is combined with nano pineapple leaf cellulose solution and other ingredients and is subjected to ultrasonic assisted emulsification and shearing so as to prepare a homogeneous membrane solution, thus preparing the pineapple cellulose film, the film has high stress tolerance, good acid and alkali stability, excellent thermal stability and good biodegradability.
Description
Technical field
The present invention relates to arghan packaging film technical field, particularly relate to a kind of new welan gum blending and modifying Pullulan
Polysaccharide graft pina fibre packaging film and preparation method thereof.
Background technology
With cellulose as raw material, the different macromolecule member material of processability is at necks such as medical science, biology and food medicine
Territory plays an important role, and has become as the focus of current research.China often produces substantial amounts of Fructus Ananadis comosi per year, and arghan has
The health-care effecies such as antibacterial, smelly eliminating, utilize arghan to prepare macromolecule member material and have huge development prospect.Pineapple leaves is fine
The fiber macromolecular alignment of dimension crystallization song is neat, regular, and the polyhydroxy structure of fiber molecule and strong hydrogen bonding effect make it clean
Cleanliness and the degree of orientation are higher, and chemical reactivity is low, thus cause its application to be restricted." the agriculture in south such as Wei Xiaoyi, Yang Qin
Journal ", 2016,47(1): 101-106 " arghan element film preparation process optimization " utilizes emulsifying cut mode to make pineapple leaves
Cellulose dissolution improves the chemical reactivity of arghan in ionic liquid, it is achieved the preparation of cellulose membrane, specifically does
Method is: be ground into cotton shape with Universalpulverizer after first being dried by arghan element, and alkali processes and acid treatment realizes it respectively
Purification process, is then being placed in together with ionic liquid in mulser, is carrying out shear treatment, acquisition prepare the cellulose of film from
Sub-liquid homogeneous phase solution, is layered on homogeneous phase solution on the carrier scribbling politef afterwards, through casting solution (glycerol, second
Alcohol) etc. soak drying and forming-film;This process technique improves the chemical reaction activity of arghan element, improves the equal of coating solution
Phase, but operate and employ substantial amounts of acidizer and alkali inorganic agent, adds somewhat to pollute, add Fructus Ananadis comosi
Leaf fibre element film preparation cost, the cellulose membrane function singleness simultaneously prepared.Nano-cellulose have high-crystallinity, high intensity,
The excellent properties such as high-specific surface area, environmental friendliness and low cost, also exist substantial amounts of-OH in its molecular structure, with other skies
So macromole is easily formed intermolecular and intramolecular hydrogen bond when being blended, and when being used for making membrane material, can make the formation of intermingling material
Membrane structure more stable.Micro-nano bubble refers to that diameter is between micron bubble (bubble of a diameter of 10-50um in water body)
And the bubble between nano bubble (a diameter of bubble less than 200nm in water body), have big specific surface area, can be at water
In body, the time of staying is long, and micro-nano bubble is when shrinking, it is possible to produce substantial amounts of hydroxyl radical free radical, these substantial amounts of hydroxyls
Free radical can attract the hydrogen bond in arghan element to a certain extent, plays equivalent acidifying alkalization and destroys the effect that hydrogen bond is identical
Really, the nanorize promoting arghan is improved its chemical reaction activity and there is certain facilitation.Pulullan polysaccharide is
The polymer substance of colorless and odorless odorless, has edibility and biodegradability, has good film property, the thin film tool made
There are good gas barrier property and water preventing ability, but containing substantial amounts of hydrophilic radical on pulullan polysaccharide strand, can be with other
Fibrous material combines the fibrous membrane prepared, but these fibrous membranes chance water is instant, limits its application on some packaging films;
The fibrous membrane that arghan based on modified pulullan polysaccharide and high chemical reactivity combines is to improving pineapple leaves
Comprehensive utilization and abundant packaging film kind are significant.
Summary of the invention
The object of the invention is contemplated to make up the defect of prior art, it is provided that a kind of new welan gum blending and modifying Pullulan is many
Sugar grafting pina fibre packaging film and preparation method thereof.
The present invention is achieved by the following technical solutions:
A kind of new welan gum blending and modifying pulullan polysaccharide grafting pina fibre packaging film, including following parts by weight of component: Fructus Ananadis comosi
Leaf fibre 125-130, compound cellulase 6-6.5, nano oxidized magnesium particle 2.8-3, citric acid 4.4-4.5, new welan gum 19-
20, pulullan polysaccharide 26-28, nano-graphene 4-5, ethylene glycol 4-5, lentinan 9-10, coconut palm leaf fibre element 19-20, diformazan
Base silicone oil 5-6, propylgallate 4-5, appropriate water, appropriate deionized water.
A kind of new welan gum blending and modifying pulullan polysaccharide grafting pina fibre packaging film preparation method, including following step
Rapid:
(1), will arghan dry after become cotton shape by pulverization process 30min in Universalpulverizer, afterwards with citric acid with
And the water mixing and stirring of gross weight 4 times to obtain slurry standby, slurry is heated to 60 DEG C, and is continuously added into compound cellulase
Mix and blend enzymolysis 40min, after 100 DEG C of enzyme denaturing 5min, vacuum filtration is also washed, and obtains purification arghan, by purification Fructus Ananadis comosi
Leaf fibre adds nano oxidized magnesium particle and the deionized water of gross weight 10 times, then at the high pressure homogenize machinery of 700bar
Under reason 30min, 1400W power, strength supersound process 50min, obtains uniform mixed liquor, is using intermittent steam blasting procedure explosion
Process this uniform mixed liquor 5 times, each 10min, obtain nanorize arghan cellulose solution standby;
(2), the deionized water of new welan gum, ethylene glycol and gross weight 0.5 times is mixed, 100 DEG C of heated and stirred 40min,
It is subsequently adding nano-graphene stirring 10min and obtains the modified new welan gum of nano-graphene, add pulullan polysaccharide, 60 afterwards
DEG C heated and stirred 20min, cooling, it is standby that mill-drying obtains new welan gum blending and modifying pulullan polysaccharide;
(3), by nanorize arghan cellulose solution, new welan gum blending and modifying pulullan polysaccharide, lentinan, coconut palm leaf fibre
Stir after the deionized water mixing of element, dimethicone, propylgallate and gross weight 3-4 times, be then placed in band
Have in the mulser of intense ultrasonic wave and carry out ultrasonic assistant emulsifying shear treatment 40min, then carry out the microwave treatment of 350W
3min, obtains emulsifying homogeneous membrane solution for standby, wherein ultrasonic power 1000W, emulsifying shear rate 15000r/min;
(4), by emulsifying homogeneous membrane solution using and scrape form membrane and be layered on glass substrate, film thickness is 1mm, then at 50-55 DEG C
Under, humidity be 55-60% calorstat in be dried 3-4h, to obtain final product.
The invention have the advantage that
The present invention use the pulullan polysaccharide of new welan gum blending and modifying combine nanorize arghan cellulose solution and other
Composition is sheared preparation emulsifying homogeneous membrane solution through ultrasonic assistant emulsifying and is prepared pina fibre element film, has high resistance, real
Having showed the application at packaging film Material Field of pina fibre element and pulullan polysaccharide, the cellulose membrane of preparation is because using nanorize
Pina fibre cellulose solution, has good breathability and spatial structure, and the shearing that the new welan gum of employing has excellence is dilute
Release effect, excellent Efficient Adhesive Promotion, good salt tolerance, good ph stability, excellent heat stability and can be biological
Degradability, can increase the resistance of film, in a heated condition it is carried out surface modification, then by adding nano-graphene
Use it for the blending and modifying of pulullan polysaccharide, it is achieved that the modification that pulullan polysaccharide hydrophilic reduces, improve film property, change
Pulullan polysaccharide after property is combined is prepared as homogeneous liquid with nanometer arghan and coconut palm leaf fibre element, is further prepared into packaging
Film;For the problem that arghan chemical reaction activity is low, have employed enzyme purification, highly active nano oxidized magnesium particle successively
Additional high pressure homogenizing, strong supersound process and intermittent steam blasting procedure explosion treatment, it is achieved that the purification of arghan with
And nanorize, lay a good foundation for preparing high performance arghan film;For the homogeneous problem of coating solution, use the most ultrasonic
Processing the mode coordinating emulsifying to shear, strong supersound process improves the content of micro-nano bubble in coating solution, helps lend some impetus to each
The dissolving of material, improves the homogeneous of membrane material solution.
Detailed description of the invention
A kind of new welan gum blending and modifying pulullan polysaccharide grafting pina fibre packaging film, including following parts by weight of component:
Arghan 125, compound cellulase 6, nano oxidized magnesium particle 2.8, citric acid 4.4, new welan gum 19, pulullan polysaccharide
26, nano-graphene 4, ethylene glycol 4, lentinan 9, coconut palm leaf fibre element 19, dimethicone 5, propylgallate 4, appropriate
Water, appropriate deionized water.
A kind of new welan gum blending and modifying pulullan polysaccharide grafting pina fibre packaging film preparation method, including following step
Rapid:
(1), will arghan dry after become cotton shape by pulverization process 30min in Universalpulverizer, afterwards with citric acid with
And the water mixing and stirring of gross weight 4 times to obtain slurry standby, slurry is heated to 60 DEG C, and is continuously added into compound cellulase
Mix and blend enzymolysis 40min, after 100 DEG C of enzyme denaturing 5min, vacuum filtration is also washed, and obtains purification arghan, by purification Fructus Ananadis comosi
Leaf fibre adds nano oxidized magnesium particle and the deionized water of gross weight 10 times, then at the high pressure homogenize machinery of 700bar
Under reason 30min, 1400W power, strength supersound process 50min, obtains uniform mixed liquor, is using intermittent steam blasting procedure explosion
Process this uniform mixed liquor 5 times, each 10min, obtain nanorize arghan cellulose solution standby;
(2), the deionized water of new welan gum, ethylene glycol and gross weight 0.5 times is mixed, 100 DEG C of heated and stirred 40min,
It is subsequently adding nano-graphene stirring 10min and obtains the modified new welan gum of nano-graphene, add pulullan polysaccharide, 60 afterwards
DEG C heated and stirred 20min, cooling, it is standby that mill-drying obtains new welan gum blending and modifying pulullan polysaccharide;
(3), by nanorize arghan cellulose solution, new welan gum blending and modifying pulullan polysaccharide, lentinan, coconut palm leaf fibre
Element, dimethicone, propylgallate and gross weight 3 times deionized water mixing after stir, be then placed in
The mulser of intense ultrasonic wave carries out ultrasonic assistant emulsifying shear treatment 40min, then carries out microwave treatment 3min of 350W,
Obtain emulsifying homogeneous membrane solution for standby, wherein ultrasonic power 1000W, emulsifying shear rate 15000r/min;
(4), by emulsifying homogeneous membrane solution using and scrape form membrane and be layered on glass substrate, film thickness is 1mm, then at 50 DEG C,
Humidity be 55% calorstat in be dried 3h, to obtain final product.
After tested, this packaging film impingement rate is 19.20kJ/m2, and anti-to stretch intensity be 28.5MPa, elongation at break 43.2%,
The OTR oxygen transmission rate of film is reached for 3.48 × 10-5cm3/ (m2 d Pa), and after soil buries 150d, its biological degradation rate reaches 96.6%, aobvious
Excellent biological degradability is shown.
Claims (2)
1. a new welan gum blending and modifying pulullan polysaccharide grafting pina fibre packaging film, it is characterised in that include following heavy
Amount part component: arghan 125-130, compound cellulase 6-6.5, nano oxidized magnesium particle 2.8-3, citric acid 4.4-
4.5, new welan gum 19-20, pulullan polysaccharide 26-28, nano-graphene 4-5, ethylene glycol 4-5, lentinan 9-10, coconut palm leaf fibre
Dimension element 19-20, dimethicone 5-6, propylgallate 4-5, appropriate water, appropriate deionized water.
2. a new welan gum blending and modifying pulullan polysaccharide grafting pina fibre packaging film preparation method, it is characterised in that bag
Include following steps:
(1), will arghan dry after become cotton shape by pulverization process 30min in Universalpulverizer, afterwards with citric acid with
And the water mixing and stirring of gross weight 4 times to obtain slurry standby, slurry is heated to 60 DEG C, and is continuously added into compound cellulase
Mix and blend enzymolysis 40min, after 100 DEG C of enzyme denaturing 5min, vacuum filtration is also washed, and obtains purification arghan, by purification Fructus Ananadis comosi
Leaf fibre adds nano oxidized magnesium particle and the deionized water of gross weight 10 times, then at the high pressure homogenize machinery of 700bar
Under reason 30min, 1400W power, strength supersound process 50min, obtains uniform mixed liquor, is using intermittent steam blasting procedure explosion
Process this uniform mixed liquor 5 times, each 10min, obtain nanorize arghan cellulose solution standby;
(2), the deionized water of new welan gum, ethylene glycol and gross weight 0.5 times is mixed, 100 DEG C of heated and stirred 40min,
It is subsequently adding nano-graphene stirring 10min and obtains the modified new welan gum of nano-graphene, add pulullan polysaccharide, 60 afterwards
DEG C heated and stirred 20min, cooling, it is standby that mill-drying obtains new welan gum blending and modifying pulullan polysaccharide;
(3), by nanorize arghan cellulose solution, new welan gum blending and modifying pulullan polysaccharide, lentinan, coconut palm leaf fibre
Stir after the deionized water mixing of element, dimethicone, propylgallate and gross weight 3-4 times, be then placed in band
Have in the mulser of intense ultrasonic wave and carry out ultrasonic assistant emulsifying shear treatment 40min, then carry out the microwave treatment of 350W
3min, obtains emulsifying homogeneous membrane solution for standby, wherein ultrasonic power 1000W, emulsifying shear rate 15000r/min;
(4), by emulsifying homogeneous membrane solution using and scrape form membrane and be layered on glass substrate, film thickness is 1mm, then at 50-55 DEG C
Under, humidity be 55-60% calorstat in be dried 3-4h, to obtain final product.
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Cited By (1)
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CN111647205A (en) * | 2020-06-24 | 2020-09-11 | 武汉海吉亚生物科技有限公司 | Edible film and preparation method and application thereof |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103102419A (en) * | 2013-01-25 | 2013-05-15 | 浙江理工大学 | Method for preparing nano microcrystalline cellulose by hydrolyzing phyllostachys edulis fiber with cellulase |
CN103254469A (en) * | 2013-06-08 | 2013-08-21 | 中国国旅贸易有限责任公司 | Edible film material containing nanocellulose, edible film and preparation method of edible film |
-
2016
- 2016-07-04 CN CN201610518833.6A patent/CN106046424A/en not_active Withdrawn
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103102419A (en) * | 2013-01-25 | 2013-05-15 | 浙江理工大学 | Method for preparing nano microcrystalline cellulose by hydrolyzing phyllostachys edulis fiber with cellulase |
CN103254469A (en) * | 2013-06-08 | 2013-08-21 | 中国国旅贸易有限责任公司 | Edible film material containing nanocellulose, edible film and preparation method of edible film |
Non-Patent Citations (1)
Title |
---|
魏晓奕等: ""菠萝叶纤维素膜制备工艺优化"", 《南方农业学报》 * |
Cited By (1)
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---|---|---|---|---|
CN111647205A (en) * | 2020-06-24 | 2020-09-11 | 武汉海吉亚生物科技有限公司 | Edible film and preparation method and application thereof |
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Application publication date: 20161026 |