CN107353503A - Biodegradable packaging box and preparation method thereof - Google Patents

Biodegradable packaging box and preparation method thereof Download PDF

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Publication number
CN107353503A
CN107353503A CN201710721964.9A CN201710721964A CN107353503A CN 107353503 A CN107353503 A CN 107353503A CN 201710721964 A CN201710721964 A CN 201710721964A CN 107353503 A CN107353503 A CN 107353503A
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preparation
parts
acid
pla
lubricant
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钱万水
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Wuhu Blue Sky Project Plastic Cement Co Ltd
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Wuhu Blue Sky Project Plastic Cement Co Ltd
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Priority to CN201710721964.9A priority Critical patent/CN107353503A/en
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • C08L23/12Polypropene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/92Measuring, controlling or regulating
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/91Polymers modified by chemical after-treatment
    • C08G63/912Polymers modified by chemical after-treatment derived from hydroxycarboxylic acids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C2948/00Indexing scheme relating to extrusion moulding
    • B29C2948/92Measuring, controlling or regulating
    • B29C2948/92504Controlled parameter
    • B29C2948/92704Temperature
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2237Oxides; Hydroxides of metals of titanium
    • C08K2003/2241Titanium dioxide
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/06Biodegradable
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • C08L2205/035Polymer 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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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Biological Depolymerization Polymers (AREA)

Abstract

The invention discloses a kind of biodegradable packaging box and preparation method thereof, the present invention is participated in using dihydric alcohol and binary acid and the polymerisation of PLA, improve alcoholic extract hydroxyl group in PLA, carboxyl, the quantity of ester group isoreactivity group, increase degradable basic point, simultaneously, titanium dioxide, octyl ferrocene, the addition of polypropylene and lubricant, the overall mechanical performance of material is improved again, in above-mentioned preparation method, by plasma-induced, add the activity of degradable basic point, improve the degradable efficiency of material, further expressing technique improves the mechanical performance of material.Meanwhile this method is simple, cost of material is low, has preferable application value.

Description

Biodegradable packaging box and preparation method thereof
Technical field
The present invention relates to biodegradable packaging box, in particular it relates to biodegradable packaging box and preparation method thereof.
Background technology
Plastics are a kind of cheap and good-quality materials, however as widely using for polybag and plastics thin article, Ren Menfa The inherent life-span of existing plastics thin article is considerably longer than its service life.In plastics durability, make it in urban solid garbage Ratio rise, the plastics thin article (such as polybag, plastics package, disposable plastic articles for use, mulch film) arbitrarily abandoned be even more Environment is polluted for a long time, is increasingly becoming white pollution, turns into 21st century puzzlement human survival and the great difficulty of development One of topic.The development, increasing packing box etc. that particularly current fast food net business takes out is pending.
In order to reduce white pollution, preserve the ecological environment, the research of biodegradable plastics, exploitation and more next using seeming It is more important and urgent.But biodegradable plastics tool still has the following disadvantages:(1) most of is PLA base material, can biology The high expensive of degradative plastics;(2) physical and mechanical property of biodegradable plastics is poor, its tensile strength, elongation at break, top Broken and tearing strength etc. does not all reach the requirement of packing box application, influences its application.
The mechanical performance of biodegradable packaging box how is improved, while is reduced with the production cost of biodegradable packaging box, being can Degradable package box is promoted, and the cheap, plastic products of lightweight, high specific strength, health can be continuing with by making us class, and and can is kept away Exempt from the key of white pollution.
The content of the invention
The purpose of the present invention is biodegradable packaging box and preparation method thereof, and the material is using polypropylene as matrix, by PLA The material formed with binary acid and dihydric alcohol combines, and has more degradable basic point, another aspect, polypropylene and other Component is combined, and is improved the overall mechanical performance of material, has been expanded biodegradable packaging box application.
To achieve these goals, the invention provides a kind of preparation method of biodegradable packaging box, the preparation method Comprise the following steps:(1) PLA, dihydric alcohol are subjected to prepolymerization, then add binary acid and butyl stannonic acid, polymerize; (2) gained mixture in step (1) is carried out plasma-induced;(3) mixture after being handled in step (2) is added to stirring In machine, titanium dioxide, octyl ferrocene, polypropylene and lubricant are added, is further continued for stirring;(4) by step (3) processing Mixture afterwards adds in double screw extruder and carries out extruding pelletization;(5) by the degradable grain injection molding in step (4).
The present invention also provides a kind of biodegradable packaging box prepared according to previously described preparation method.
In the above-mentioned technical solutions, the present invention improves using dihydric alcohol and the polymerisation of binary acid participation and PLA Alcoholic extract hydroxyl group, carboxyl, the quantity of ester group isoreactivity group in PLA, increase degradable basic point, meanwhile, titanium dioxide, The addition of octyl ferrocene, polypropylene and lubricant, the overall mechanical performance of material is improved again, in above-mentioned preparation technology In, by plasma-induced, the activity of degradable basic point is added, improves the degradable efficiency of material, further extrusion Technique improves the mechanical performance of material.Meanwhile this method is simple, cost of material is low, has preferable application value.
Other features and advantages of the present invention will be described in detail in subsequent specific embodiment part.
Embodiment
The embodiment of the present invention is described in detail below.It is it should be appreciated that described herein specific Embodiment is merely to illustrate and explain the present invention, and is not intended to limit the invention.
The end points of disclosed scope and any value are not limited to the accurate scope or value herein, these scopes or Value should be understood to comprising the value close to these scopes or value.For number range, between the endpoint value of each scope, respectively It can be combined with each other between the endpoint value of individual scope and single point value, and individually between point value and obtain one or more New number range, these number ranges should be considered as specific open herein.
The invention provides a kind of preparation method of biodegradable packaging box, the preparation method comprises the following steps:(1) will PLA, dihydric alcohol carry out prepolymerization, then add binary acid and butyl stannonic acid, are polymerize;(2) by gained in step (1) Mixture carries out plasma-induced;(3) mixture after being handled in step (2) is added in mixer, addition titanium dioxide, Octyl ferrocene, polypropylene and lubricant, it is further continued for stirring;(4) mixture after step (3) processing is added into double spiral shells Extruding pelletization is carried out in bar extruder;(5) by the degradable grain injection molding in step (4).
In the above-mentioned technical solutions, the present invention improves using dihydric alcohol and the polymerisation of binary acid participation and PLA Alcoholic extract hydroxyl group, carboxyl, the quantity of ester group isoreactivity group in PLA, increase degradable basic point, meanwhile, titanium dioxide, The addition of octyl ferrocene, polypropylene and lubricant, the overall mechanical performance of material is improved again, in above-mentioned preparation technology In, by plasma-induced, the activity of degradable basic point is added, improves the degradable efficiency of material, further extrusion Technique improves the mechanical performance of material.Meanwhile this method is simple, cost of material is low, has preferable application value.
Certainly, in the above-mentioned technical solutions, the amount of the addition of each component can be adjusted in relative broad range, in order to ensure Material has preferable mechanical performance, while has good degradability, furthermore it is preferred that in parts by weight, PLA 5- 15 parts, dihydric alcohol 4-6 parts, binary acid 5-8 parts, butyl stannonic acid 2-3 parts, titanium dioxide 0.5-0.8 parts, octyl ferrocene 0.2- 0.5 part, polypropylene 30-40 parts, lubricant 3-5 parts.So, biodegradable packaging box is mainly polypropylene with base material in material, and Low in the degradation material of the more conventional PLA base material of amount of the addition of PLA, still, the degradability of material is not It is decreased obviously, the mechanical performance of the opposing party's material disclosure satisfy that requirement of the daily plastic products to the mechanical property of materials.
In the above-mentioned technical solutions, the number-average molecular weight of PLA can be adjusted in relative broad range, poly- in order to improve Lactic acid and binary acid polymerize basic point quantity with dihydric alcohol, it is preferable that the relatively low PLA of selective polymerization degree, it is more excellent in the present invention In the embodiment of choosing, the number-average molecular weight of the PLA of PLA is 4000-12000.
Moreover, dihydric alcohol can be selected in relative broad range, excellent in order to improve polymerization basic point quantity in polymer Selection of land, dihydric alcohol are the one or more in ethylene glycol, BDO, 1,2-PD and 1,3-PD.
Binary acid can be selected in relative broad range, in order to improve polymerization basic point quantity in polymer, it is preferable that binary Acid is the one or more in succinic acid, glutaric acid and adipic acid.
For polyacrylic molecular weight, those skilled in the art can be selected in relative broad range, in order to improve poly- third The syncretizing effect of alkene and PLA, it is preferable that the relatively low polypropylene of selective polymerization degree, in the preferred embodiment of the present invention In, polyacrylic number-average molecular weight is 10000-15000.
In addition, lubricant can select in relative broad range, plastic products conventional lubricantss may be selected, in order to improve material Syncretizing effect, while the toughness of reinforcing material, it is preferable that lubricant is stearic acid, hydroxy stearic acid, n-butyl stearate, list Glyceryl stearate, methyl hydroxystearate, soybean oil, peanut oil, corn oil, rice bran oil, rapeseed oil, cottonseed oil, sunflower seeds One or more in oil and camellia seed oil.
For plasma-induced condition, those skilled in the art can be selected in relative broad range, in order to improve base The quantity of the polymerization activity basic point on material surface, it is preferable that plasma-induced condition includes:The mixture that step (1) is obtained Insert on the bottom electrode medium of plasma device, in voltage 115-125kV, electric current 24-26mA, gap is 4-6mm operation Under the conditions of irradiate.So, using initial stage, material is because surface aggregate is fine and close, and mechanical strength is higher, after use, due to positioned at material Expect the fracture of the chemical bond of the polymerization activity basic point on surface, improve the degradation property of material.
Certainly, in above-mentioned embodiment, plasma-induced irradiation time can be adjusted in relative broad range, In order to improve the quantity of the polymerization activity basic point of substrate surface, material premature breakdown is on the other hand prevented, at one of the invention more In preferred embodiment, plasma-induced condition is 1.5-3min including irradiation time.
Moreover, can be adjusted for prepolymerized condition in step (1), those skilled in the art in relative broad range It is whole, in order to improve prepolymerization efficiency, improve the quantity of active basic point in PLA, it is preferable that prepolymerized condition includes:In 70-90 DEG C in 100-120rpm prepolymerizations.
Wherein, prepolymerization time can be adjusted in relative broad range, in preferred embodiment of the invention, preferably Ground, prepolymerization 15-25min.
For the condition of polymerization in step (1), those skilled in the art can be adjusted in relative broad range, in order to improve Prepolymerization efficiency, improve the quantity of active basic point in PLA, it is preferable that prepolymerized condition includes:By temperature adjust to 180-220 DEG C polymerize in 240-320rpm.
Wherein, polymerization time can be adjusted in relative broad range, in preferred embodiment of the invention, preferably Ground, it polymerize 20-30min.
Stirring condition in step (3) can be adjusted in relative broad range, in order to improve the syncretizing effect of material, preferably Ground, the mixture after being handled in step (2) is added in mixer, adds titanium dioxide, octyl ferrocene and polypropylene, Stir at a certain temperature, then cooling adds lubricant, is stirred for discharging after being well mixed.In this paper preferred embodiments In, in order to improve the syncretizing effect of material, it is preferable that the mixture after being handled in step (2) is added in mixer, added Titanium dioxide, octyl ferrocene and polypropylene, stir in the 160-180 DEG C of speed with 200-240rpm, be then cooled to Lubricant is added at 130-140 DEG C, is stirred for discharging after being well mixed.
Certainly, the time of mixing can be adjusted in relative broad range, in order to improve the syncretizing effect of material, preferably Ground, titanium dioxide, octyl ferrocene and polypropylene stirring 20-30min are added, 10-20min is stirred for after adding lubricant.
For the extrusion condition in step (4), those skilled in the art can be adjusted in relative broad range, in order that thing Material is well mixed, while improves the mechanical performance of material, it is preferable that the temperature of each section of double screw extruder is 180- during extrusion 210℃。
Certainly, screw speed can be adjusted in relative broad range during extrusion, in order that material is well mixed, be improved simultaneously The mechanical performance of material, it is preferable that screw speed 250-280rpm.
In addition, blanking velocity can be adjusted in relative broad range during extrusion, in order to improve blanking efficiency, it is preferable that under Material speed is 30-40rpm.
For the injecting condition in step (5), those skilled in the art can be adjusted in relative broad range, in order that bag Mounted box uniform in shaping, it is preferable that injection temperature is 190-210 DEG C in step (5).
The temperature of mould, those skilled in the art can be adjusted in relative broad range when certainly, for being molded in step (5) It is whole, in order that packing box uniform in shaping, it is preferable that mold temperature control is at 110-140 DEG C during injection.
The present invention also provides a kind of biodegradable packaging box prepared according to previously described preparation method.
In the above-mentioned technical solutions, the present invention improves using dihydric alcohol and the polymerisation of binary acid participation and PLA Alcoholic extract hydroxyl group, carboxyl, the quantity of ester group isoreactivity group in PLA, increase degradable basic point, meanwhile, titanium dioxide, The addition of octyl ferrocene, polypropylene and lubricant, the overall mechanical performance of material is improved again.Meanwhile cost of material is low, With preferable application value.
The present invention will be described in detail by way of examples below.The number-average molecular weight of PLA is 8000;Polypropylene Number-average molecular weight be 12000;Other are conventional commercial products.
Embodiment 1
The preparation method of biodegradable packaging box, comprises the following steps:
(1) by 5 parts of PLA, 4 parts of 1,2-PD in 100rpm prepolymerization 15min, then adds succinic acid 5 in 70 DEG C 2 parts of part and butyl stannonic acid, temperature is adjusted to 180 DEG C and polymerize 20min in 240rpm;
(2) mixture obtained in step (1) is inserted on the bottom electrode medium of plasma device, in voltage 115kV, Electric current 24mA, gap are to irradiate 1.5min under 4mm operating condition;
(3) mixture after being handled in step (2) is added in mixer, adds 0.5 part of titanium dioxide, n-octyl two Luxuriant 0.2 part of iron, 30 parts of polypropylene stir 20min in 160 DEG C of speed with 200rpm, lubrication are added when being then cooled to 130 DEG C 3 parts of stirring 10min of agent, discharge after well mixed;
(4) mixture after step (3) processing is carried out in double screw extruder in 180 DEG C of screw speeds for 250rpm Extrusion, blanking velocity 30rpm, it is granulated;
(5) by the degradable grain in step (4), mold temperature is controlled 110 when temperature is in 190 DEG C of injection moldings, injection ℃。
Embodiment 2
The preparation method of biodegradable packaging box, comprises the following steps:
(1) by 15 parts of PLA, 6 parts of 1,2-PD in 120rpm prepolymerization 25min, then adds succinic acid in 90 DEG C 8 parts and 3 parts of butyl stannonic acid, temperature is adjusted to 220 DEG C in 320rpm polyase 13s 0min;
(2) mixture that step (1) obtains is inserted on the bottom electrode medium of plasma device, in voltage 125kV, electricity 26mA is flowed, gap is to irradiate 3min under 6mm operating condition;
(3) mixture after being handled in step (2) is added in mixer, adds 0.8 part of titanium dioxide, n-octyl two Luxuriant 0.5 part of iron, 40 parts of polypropylene stir 30min in 180 DEG C of speed with 240rpm, lubrication are added when being then cooled to 140 DEG C 5 parts of stirring 20min of agent, discharge after well mixed;
(4) mixture after step (3) processing is carried out in double screw extruder in 210 DEG C of screw speeds for 280rpm Extrusion, blanking velocity 40rpm, it is granulated;
(5) by the degradable grain in step (4), mold temperature is controlled 140 when temperature is in 210 DEG C of injection moldings, injection ℃。
Embodiment 3
The preparation method of biodegradable packaging box, comprises the following steps:
(1) by 10 parts of PLA, 5 parts of 1,2-PD in 110rpm prepolymerization 20min, then adds succinic acid in 80 DEG C 6.5 parts and 2.5 parts of butyl stannonic acid, temperature is adjusted to 200 DEG C and polymerize 25min in 280rpm;
(2) mixture that step (2) obtains is inserted on the bottom electrode medium of plasma device, in voltage 120kV, electricity 25mA is flowed, gap is to irradiate 2.25min under 5mm operating condition;
(3) mixture after being handled in step (2) is added in mixer, adds 0.65 part of titanium dioxide, n-octyl 0.35 part of ferrocene, 35 parts of polypropylene stir 25min in 170 DEG C of speed with 220rpm, profit are added when being then cooled to 135 DEG C 4 parts of stirring 15min of lubrication prescription, discharge after well mixed;
(4) mixture after step (3) processing is carried out in double screw extruder in 195 DEG C of screw speeds for 265rpm Extrusion, blanking velocity 35rpm, it is granulated;
(5) by the degradable grain in step (4), mold temperature is controlled 125 when temperature is in 200 DEG C of injection moldings, injection ℃。
Comparative example 1
Biodegradable packaging box is prepared according to the method for embodiment 3, unlike, step is added without 1,2-PD in (1) And succinic acid, step (1) is adjusted to:By PLA, 10 parts are kneaded 20min in 80 DEG C in 110rpm, then add butyl stannonic acid 2.5 parts, temperature is adjusted to 200 DEG C and is kneaded 25min in 280rpm, other conditions are same as Example 3.
Comparative example 2
Biodegradable packaging box is prepared according to the method for embodiment 3, unlike, step is added without polypropylene in (3), other Condition is same as Example 3.
Comparative example 3
Biodegradable packaging box is prepared according to the method for embodiment 3, unlike, omit step (2).
Comparative example 4
Biodegradable packaging box is prepared according to the method for embodiment 3, unlike, it is added without polypropylene in step (3), and incite somebody to action The amount of the addition of PLA is adjusted to 45 parts in step (1), and other conditions are in the same manner as in Example 3.
Detect example 1
Biodegradable packaging box degradation material is according to national standard GB/T 12914- made from embodiment 1-3 and comparative example 1-4 2008 method sample preparation, and tensile strength and elongation at break are detected, concrete outcome is shown in Table 1.
Detect example 2
100 × 50 × 5 (lists are made with degradation material in the biodegradable packaging box that embodiment 1-3 and comparative example 1-4 are obtained Position, mm) sample, be immersed in pH be 5.5 phosphate buffer in, place 60 days.The weight of sample before and after testing is weighed, is calculated Degradation rate, concrete outcome are shown in Table 1.
Weight × 100% of sample before degradation rate=(weight of sample after weight-experiment of sample before experiment)/experiment
Table 1
Project Tensile strength/MPa Elongation at break/% Degradation rate/%
Embodiment 1 30.3 850 37
Embodiment 2 32.2 860 39
Embodiment 3 33.5 880 42
Comparative example 1 26.5 680 20
Comparative example 2 22.4 540 43
Comparative example 3 27.7 710 28
Comparative example 4 25.8 580 42
The preferred embodiment of the present invention described in detail above, still, the present invention are not limited in above-mentioned embodiment Detail, in the range of the technology design of the present invention, a variety of simple variants can be carried out to technical scheme, this A little simple variants belong to protection scope of the present invention.
It is further to note that each particular technique feature described in above-mentioned embodiment, in not lance In the case of shield, can be combined by any suitable means, in order to avoid unnecessary repetition, the present invention to it is various can The combination of energy no longer separately illustrates.
In addition, various embodiments of the present invention can be combined randomly, as long as it is without prejudice to originally The thought of invention, it should equally be considered as content disclosed in this invention.

Claims (10)

1. a kind of preparation method of biodegradable packaging box, it is characterised in that the preparation method comprises the following steps:
(1) PLA, dihydric alcohol are subjected to prepolymerization, then add binary acid and butyl stannonic acid, polymerize;
(2) gained mixture in step (1) is carried out plasma-induced;
(3) mixture after being handled in step (2) is added in mixer, adds titanium dioxide, octyl ferrocene, poly- third Alkene and lubricant, it is further continued for stirring;
(4) mixture after step (3) processing is added in double screw extruder and carries out extruding pelletization;
(5) by the degradable grain injection molding in step (4).
2. preparation method according to claim 1, wherein, in parts by weight, PLA 5-15 parts, dihydric alcohol 4-6 parts, two The sour 5-8 parts of member, butyl stannonic acid 2-3 parts, titanium dioxide 0.5-0.8 parts, octyl ferrocene 0.2-0.5 parts, polypropylene 30-40 Part, lubricant 3-5 parts.
3. the preparation method according to right wants 1 or 2, wherein, plasma-induced condition includes:Step (1) is obtained Mixture is inserted on the bottom electrode medium of plasma device, in voltage 115-125kV, electric current 24-26mA, gap 4-6mm Operating condition under irradiate 1.5-3min.
4. the preparation method according to right wants 1 or 2, wherein, prepolymerized condition includes:In 70-90 DEG C in 100- 120rpm prepolymerizations 15-25min.
5. the preparation method according to right wants 1 or 2, wherein, the condition of polymerisation includes:Temperature is adjusted to 180- 220 DEG C polymerize in 240-320rpm;
And/or polymerization 20-30min.
6. the preparation method according to right wants 1 or 2, wherein, the stirring condition in step (3) includes:It will locate in step (2) Mixture after reason is added in mixer, adds titanium dioxide, octyl ferrocene and polypropylene, in 160-180 DEG C with 200-240rpm speed stirring, lubricant is added when being then cooled to 130-140 DEG C, is stirred for discharging after being well mixed;
And/or titanium dioxide, octyl ferrocene and polypropylene stirring 20-30min are added, add mixing time after lubricant For 10-20min.
7. the preparation method according to right wants 1 or 2, wherein, extrusion condition includes in step (4):Twin-screw squeezes during extrusion The temperature for going out each section of machine is 180-210 DEG C;
And/or screw speed 250-280rpm;
And/or blanking velocity 30-40rpm.
8. the preparation method according to right wants 1 or 2, wherein, injection temperature is 190-210 DEG C in step (5);
And/or mold temperature is controlled at 110-140 DEG C during injection.
9. the preparation method according to right wants 1 or 2, wherein, the number-average molecular weight of PLA is 4000-12000;
And/or dihydric alcohol is the one or more in ethylene glycol, BDO, 1,2-PD and 1,3-PD;
And/or binary acid is the one or more in succinic acid, glutaric acid and adipic acid;
And/or polyacrylic number-average molecular weight is 10000-15000;
And/or lubricant is stearic acid, hydroxy stearic acid, n-butyl stearate, single stearic acid glycerine lipoprotein, hydroxy stearic acid first One kind or more in ester, soybean oil, peanut oil, corn oil, rice bran oil, rapeseed oil, cottonseed oil, sunflower oil and camellia seed oil Kind.
A kind of 10. biodegradable packaging box prepared by preparation method according to any one of claim 1-9.
CN201710721964.9A 2017-08-22 2017-08-22 Biodegradable packaging box and preparation method thereof Pending CN107353503A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107964224A (en) * 2017-12-15 2018-04-27 安徽悦尔伟塑料机械有限公司 The preparation method of automotive compounded door handle
CN110539971A (en) * 2019-07-09 2019-12-06 中山市金群瑞科技有限公司 Adopt packing carton of individual layer degradable carbon calcium board preparation
CN112300590A (en) * 2020-09-27 2021-02-02 宿州合鑫食品包装有限公司 Green degradable packing carton of bio-based

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102838855A (en) * 2011-06-23 2012-12-26 中国石油化工股份有限公司 Biodegradable composite, disposable product and preparation method thereof
CN106987045A (en) * 2017-05-18 2017-07-28 聂超 It is a kind of to trigger environmental protection macromolecule new material of multiple degrading and preparation method thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102838855A (en) * 2011-06-23 2012-12-26 中国石油化工股份有限公司 Biodegradable composite, disposable product and preparation method thereof
CN106987045A (en) * 2017-05-18 2017-07-28 聂超 It is a kind of to trigger environmental protection macromolecule new material of multiple degrading and preparation method thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107964224A (en) * 2017-12-15 2018-04-27 安徽悦尔伟塑料机械有限公司 The preparation method of automotive compounded door handle
CN107964224B (en) * 2017-12-15 2019-12-03 苏州睿澎诚科技有限公司 The preparation method of automotive compounded door handle
CN110539971A (en) * 2019-07-09 2019-12-06 中山市金群瑞科技有限公司 Adopt packing carton of individual layer degradable carbon calcium board preparation
CN112300590A (en) * 2020-09-27 2021-02-02 宿州合鑫食品包装有限公司 Green degradable packing carton of bio-based

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Application publication date: 20171117