CN108659313A - A kind of preparation method and applications of environment-friendly modified Pearl wool material - Google Patents
A kind of preparation method and applications of environment-friendly modified Pearl wool material Download PDFInfo
- Publication number
- CN108659313A CN108659313A CN201810505641.0A CN201810505641A CN108659313A CN 108659313 A CN108659313 A CN 108659313A CN 201810505641 A CN201810505641 A CN 201810505641A CN 108659313 A CN108659313 A CN 108659313A
- Authority
- CN
- China
- Prior art keywords
- parts
- modified pearl
- added
- environment
- preparation
- 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.)
- Withdrawn
Links
Classifications
-
- 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
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
- C08J9/141—Hydrocarbons
-
- 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
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0014—Use of organic additives
- C08J9/0023—Use of organic additives containing oxygen
-
- 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
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0066—Use of inorganic compounding ingredients
-
- 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
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/122—Hydrogen, oxygen, CO2, nitrogen or noble gases
-
- 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
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/06—CO2, N2 or noble gases
-
- 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
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/14—Saturated hydrocarbons, e.g. butane; Unspecified hydrocarbons
-
- 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
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/04—Homopolymers or copolymers of ethene
- C08J2323/06—Polyethene
-
- 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
- C08J2471/00—Characterised by the use of polyethers obtained by reactions forming an ether link in the main chain; Derivatives of such polymers
- C08J2471/02—Polyalkylene oxides
-
- 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
- C08J2497/00—Characterised by the use of lignin-containing materials
Abstract
The invention discloses a kind of preparation method and applications of environment-friendly modified Pearl wool material, this method is by talcum powder, mica powder grinding refinement, then and low density polyethylene (LDPE), lauric monoglyceride, monomethyl polyethylene glycol acrylate ester is added in reaction kettle jointly to react, again by reaction product and sodium lignin sulfonate, mutual-phenenyl two acid bromide two alcohol ester carries out microwave treatment, then by treating products with microwaves and polybutylene succinate, alumina silicate fibre carries out mixing twice and heats maintenance molten condition, then by isopropyl three (dioctylphyrophosphoric acid acyloxy) titanate esters, isooctyl acid glycidol ether is heated to molten condition, it is added into the secondary mixing product for being similarly molten condition, insulation reaction simultaneously foams, finally squeeze out while hot, it is cooling, packaging, obtain modified pearl cotton material.The modified pearl cotton material being prepared has a good application prospect still with higher tensile strength with compared with high degradability energy as packaging material.
Description
Technical field
The present invention relates to field of packaging material, and in particular to a kind of preparation method of environment-friendly modified Pearl wool material
And its application.
Background technology
Packaging material refers to meeting product packaging for manufacturing packing container, packing and decorating, packages printing, packed and transported etc.
Material used in it is required that, it had both included metal, plastics, glass, ceramics, paper, bamboo sheet, wild mushroom class, natural fiber, chemistry fibre
The main packaging material such as dimension, composite material, and include the auxiliary materials such as coating, adhesive, strapping, decoration, printing material.So
And as the industrialized development of society, all trades and professions need the packaging material being related to multifarious, type is various, while right
The demand of corresponding packaging material steeply rises.But while packaging material embodies its value in industrial society, perhaps
More drawbacks also occurs simultaneously, and frequency of use and durability be not high, and gas that is not degradable, being volatilized is harmful to environment, returns
Receipts mechanism lacks or non-recovery is worth etc..Therefore, exploitation is a kind of having the packaging material of better performance and environmental sound just
Seem particularly necessary.Pearl wool foaming material is a kind of novel environmental protection package, packing material.Its advantageous characteristic, increasingly
It is recognized, therefore its use constantly will expand and innovate.Especially in terms of packing with other industrial cut stocks, it is than passing
System uses material performance more preferable, and cost is lower, class higher, beautiful and generous, better.Pearl cotton is passed through by low density polyethylene (LDPE)
Physical blowing generates countless independent air bubble and constitutes, overcome frangible common foamed glue, deformation, restorative difference disadvantage.Pearl
Cotton have water proof is moisture-proof, shockproof, sound insulation, heat preservation, plasticity is good, toughness is strong, reconstituted circularly, environmental protection, crashworthiness power by force etc. it is many
Advantage also has good chemical resistance, is the ideal substitute of conventional packaging material.But current Pearl wool material
Still to be improved on degradation property, to further enhance its feature of environmental protection.
Invention content
In order to solve the above technical problems, the present invention provides a kind of preparation method of environment-friendly modified Pearl wool material and its answers
With, this method be by talcum powder, mica powder grinding refinement, then with low density polyethylene (LDPE), lauric monoglyceride, polyethylene glycol
Monomethyl ether acrylate is added in reaction kettle jointly to react, then by reaction product and sodium lignin sulfonate, terephthalic acid (TPA) fourth
Diol ester carries out microwave treatment, and treating products with microwaves and polybutylene succinate, alumina silicate fibre are then carried out mixing twice
And maintenance molten condition is heated, then by isopropyl three (dioctylphyrophosphoric acid acyloxy) titanate esters, isooctyl acid glycidol ether
It is heated to molten condition, is added into the secondary mixing product for being similarly molten condition, insulation reaction simultaneously foams, while hot finally
It squeezes out, is cooling, packaging, obtaining modified pearl cotton material.The modified pearl cotton material being prepared, with compared with high degradability
Still there is higher tensile strength in the case of energy, have a good application prospect as packaging material.
Technical solution:To solve the above-mentioned problems, the invention discloses a kind of preparations of environment-friendly modified Pearl wool material
Method comprises the steps of:
(1)By 5~7 parts of talcum powder, the grinding refinement of 4~6 parts of mica powder, solid grain size is made to be less than 50 μm, then with it is low close
It is common to spend 150~200 parts of polyethylene, 35~45 parts of lauric monoglyceride, 10~20 parts of monomethyl polyethylene glycol acrylate ester
It is added in reaction kettle, improves reaction kettle internal temperature and be stirred reaction to 100~120 DEG C, obtain the first reaction product;
(2)First reaction product and 16~20 parts of sodium lignin sulfonate, 8~12 parts of mutual-phenenyl two acid bromide two alcohol ester are placed in microwave
Microwave treatment is carried out in processor, obtains treating products with microwaves;
(3)Treating products with microwaves and 8~10 parts of polybutylene succinate, 2~4 parts of alumina silicate fibre are added to mixer jointly
In, mixer internal temperature is improved to 180~190 DEG C, at such a temperature internal mixing and plasticizing 40~60 minutes, is then added anti-quiet
0.5~1.5 part of electric agent improves mixer internal temperature to 250 DEG C, and secondary internal mixing and plasticizing 20~30 minutes obtains secondary close
It refines product and heats and maintain molten condition;
(4)15~25 parts of isopropyl three (dioctylphyrophosphoric acid acyloxy) titanate esters, 5~9 parts of isooctyl acid glycidol ether is mixed
Conjunction is heated to molten condition, is added into the secondary mixing product for being similarly molten condition, by temperature after being uniformly mixed
It maintains and keeps mixture in the range of molten state, 1~2 part of physical blowing agent is filled with into molten mixture, keep melting mixed
Object is closed fully to foam;
(5)Molten mixture after foaming is injected in extruder while hot, sets extruder temperature as 150 DEG C, screw speed is
80~100 revs/min, extruder pressure is 50 MPa, and modified pearl cotton material is obtained after extruded, cooling, packaging.
Further, the step(1)Middle mixed material is preferably stirred with 200~300 revs/min of rate in a kettle
Mix reaction 25~35 minutes.
Further, the step(2)The microwave frequency of middle microwave treatment be 280~300 MHz, processing time be 15~
25 minutes.
Further, the step(3)In antistatic agent to be selected from cationic antistatic agent, anionic antistatic
Any one in agent and non-ionic antistatic agent.
Further, the step(4)In physical blowing agent it is any one in butane, hexane and carbon dioxide
Kind.
At the same time, the invention also discloses environment-friendly modified Pearl wool materials made from above-mentioned preparation method as packaging
The application of material.
Compared with prior art, the present invention advantage is:
(1)The present invention environment-friendly modified Pearl wool material preparation method be by talcum powder, mica powder grinding refinement, then with
Low density polyethylene (LDPE), lauric monoglyceride, monomethyl polyethylene glycol acrylate ester are added in reaction kettle jointly to react, then will
Reaction product and sodium lignin sulfonate, mutual-phenenyl two acid bromide two alcohol ester carry out microwave treatment, then by treating products with microwaves with it is poly-
Butylene succinate, alumina silicate fibre carry out mixing twice and heat maintenance molten condition, and then by isopropyl three, (dioctyl is burnt
Phosphoric acid acyloxy) titanate esters, isooctyl acid glycidol ether be heated to molten condition, and it is added into and is similarly the secondary of molten condition
In mixing product, insulation reaction simultaneously foams, and finally squeezes out while hot, is cooling, packaging, obtaining modified pearl cotton material.It is prepared
Modified pearl cotton material, still with higher tensile strength with compared with high degradability energy, as packing timber
Material has a good application prospect.
(2)Present invention employs mutual-phenenyl two acid bromide two alcohol ester, isopropyl three (dioctylphyrophosphoric acid acyloxy) titanate esters,
The participation of isooctyl acid glycidol ether prepares environment-friendly modified Pearl wool material, and effective performance has been carried out to modified pearl cotton material
It is promoted, although these materials are not first Application in modified pearl cotton material, according to a certain ratio after amount combination, is aided with phase
The processing mode answered brings increasing substantially in performance to the modified pearl cotton material being finally prepared, this
It is never to report in previous research, for realizing that it is conclusive that the technique effect of the present invention plays the role of.
Specific implementation mode
Embodiment 1
(1)By 5 parts of talcum powder, the grinding refinement of 4 parts of mica powder, solid grain size is made to be less than 50 μm, then and low density polyethylene
150 parts of alkene, 35 parts of lauric monoglyceride, 10 parts of monomethyl polyethylene glycol acrylate ester are added in reaction kettle jointly, are improved
Reaction kettle internal temperature is stirred to react 25 minutes with 200 revs/min of rate to 100 DEG C, obtains the first reaction product;
(2)First reaction product and 16 parts of sodium lignin sulfonate, 8 parts of mutual-phenenyl two acid bromide two alcohol ester are placed in microwave treater
Microwave treatment is carried out, microwave frequency is 280 MHz, and processing time is 15 minutes, obtains treating products with microwaves;
(3)Treating products with microwaves and 8 parts of polybutylene succinate, 2 parts of alumina silicate fibre are added in mixer jointly, it will be close
Mill internal temperature is improved to 180 DEG C, at such a temperature internal mixing and plasticizing 40 minutes, and cationic antistatic agent 0.5 is then added
Part, mixer internal temperature is improved to 250 DEG C, secondary internal mixing and plasticizing 20 minutes obtains secondary mixing product and heats maintenance
In molten condition;
(4)15 parts of isopropyl three (dioctylphyrophosphoric acid acyloxy) titanate esters, 5 parts of isooctyl acid glycidol ether are mixed and heated to
Molten condition is added into the secondary mixing product for being similarly molten condition, temperature is maintained guarantor after being uniformly mixed
Mixture is held in the range of molten state, 1 part of butane foaming agent is filled with into molten mixture, molten mixture is made fully to send out
Bubble;
(5)Molten mixture after foaming is injected in extruder while hot, sets extruder temperature as 150 DEG C, screw speed is
80 revs/min, extruder pressure is 50 MPa, and modified pearl cotton material is obtained after extruded, cooling, packaging.
Embodiment 2
(1)By 6 parts of talcum powder, the grinding refinement of 5 parts of mica powder, solid grain size is made to be less than 50 μm, then and low density polyethylene
175 parts of alkene, 40 parts of lauric monoglyceride, 15 parts of monomethyl polyethylene glycol acrylate ester are added in reaction kettle jointly, are improved
Reaction kettle internal temperature is stirred to react 30 minutes with 250 revs/min of rate to 110 DEG C, obtains the first reaction product;
(2)First reaction product and 18 parts of sodium lignin sulfonate, 10 parts of mutual-phenenyl two acid bromide two alcohol ester are placed in microwave treater
Middle carry out microwave treatment, microwave frequency are 290 MHz, and processing time is 20 minutes, obtains treating products with microwaves;
(3)Treating products with microwaves and 9 parts of polybutylene succinate, 3 parts of alumina silicate fibre are added in mixer jointly, it will be close
Mill internal temperature is improved to 185 DEG C, at such a temperature internal mixing and plasticizing 50 minutes, and 1 part of anionic antistatic agent is then added,
Mixer internal temperature is improved to 250 DEG C, secondary internal mixing and plasticizing 25 minutes, obtain secondary mixing product and heating maintain it is molten
Melt state;
(4)20 parts of isopropyl three (dioctylphyrophosphoric acid acyloxy) titanate esters, 7 parts of isooctyl acid glycidol ether are mixed and heated to
Molten condition is added into the secondary mixing product for being similarly molten condition, temperature is maintained guarantor after being uniformly mixed
Mixture is held in the range of molten state, 1.5 parts of hexane foaming agent is filled with into molten mixture, molten mixture is made fully to send out
Bubble;
(5)Molten mixture after foaming is injected in extruder while hot, sets extruder temperature as 150 DEG C, screw speed is
90 revs/min, extruder pressure is 50 MPa, and modified pearl cotton material is obtained after extruded, cooling, packaging.
Embodiment 3
(1)By 7 parts of talcum powder, the grinding refinement of 6 parts of mica powder, solid grain size is made to be less than 50 μm, then and low density polyethylene
200 parts of alkene, 45 parts of lauric monoglyceride, 20 parts of monomethyl polyethylene glycol acrylate ester are added in reaction kettle jointly, are improved
Reaction kettle internal temperature is stirred to react 35 minutes with 300 revs/min of rate to 120 DEG C, obtains the first reaction product;
(2)First reaction product and 20 parts of sodium lignin sulfonate, 12 parts of mutual-phenenyl two acid bromide two alcohol ester are placed in microwave treater
Middle carry out microwave treatment, microwave frequency are 300 MHz, and processing time is 25 minutes, obtains treating products with microwaves;
(3)Treating products with microwaves and 10 parts of polybutylene succinate, 4 parts of alumina silicate fibre are added in mixer jointly, it will
Mixer internal temperature is improved to 190 DEG C, and internal mixing and plasticizing 60 minutes, are then added non-ionic antistatic agent at such a temperature
1.5 parts, mixer internal temperature is improved to 250 DEG C, secondary internal mixing and plasticizing 30 minutes obtains secondary mixing product and heats dimension
It holds in molten condition;
(4)25 parts of isopropyl three (dioctylphyrophosphoric acid acyloxy) titanate esters, 9 parts of isooctyl acid glycidol ether are mixed and heated to
Molten condition is added into the secondary mixing product for being similarly molten condition, temperature is maintained guarantor after being uniformly mixed
Mixture is held in the range of molten state, 2 parts of carbon dioxide foaming agent is filled with into molten mixture, keeps molten mixture abundant
Foaming;
(5)Molten mixture after foaming is injected in extruder while hot, sets extruder temperature as 150 DEG C, screw speed is
100 revs/min, extruder pressure is 50 MPa, and modified pearl cotton material is obtained after extruded, cooling, packaging.
Comparative example 1
(1)By 5 parts of talcum powder, the grinding refinement of 4 parts of mica powder, solid grain size is made to be less than 50 μm, then and low density polyethylene
150 parts of alkene, 35 parts of lauric monoglyceride, 10 parts of monomethyl polyethylene glycol acrylate ester are added in reaction kettle jointly, are improved
Reaction kettle internal temperature is stirred to react 25 minutes with 200 revs/min of rate to 100 DEG C, obtains the first reaction product;
(2)16 parts of first reaction product and sodium lignin sulfonate are placed in microwave treater and carry out microwave treatment, microwave frequency
For 280 MHz, processing time is 15 minutes, obtains treating products with microwaves;
(3)Treating products with microwaves and 8 parts of polybutylene succinate, 2 parts of alumina silicate fibre are added in mixer jointly, it will be close
Mill internal temperature is improved to 180 DEG C, at such a temperature internal mixing and plasticizing 40 minutes, and cationic antistatic agent 0.5 is then added
Part, mixer internal temperature is improved to 250 DEG C, secondary internal mixing and plasticizing 20 minutes obtains secondary mixing product and heats maintenance
In molten condition;
(4)15 parts of isopropyl three (dioctylphyrophosphoric acid acyloxy) titanate esters, 5 parts of isooctyl acid glycidol ether are mixed and heated to
Molten condition is added into the secondary mixing product for being similarly molten condition, temperature is maintained guarantor after being uniformly mixed
Mixture is held in the range of molten state, 1 part of butane foaming agent is filled with into molten mixture, molten mixture is made fully to send out
Bubble;
(5)Molten mixture after foaming is injected in extruder while hot, sets extruder temperature as 150 DEG C, screw speed is
80 revs/min, extruder pressure is 50 MPa, and modified pearl cotton material is obtained after extruded, cooling, packaging.
Comparative example 2
(1)By 5 parts of talcum powder, the grinding refinement of 4 parts of mica powder, solid grain size is made to be less than 50 μm, then and low density polyethylene
150 parts of alkene, 35 parts of lauric monoglyceride, 10 parts of monomethyl polyethylene glycol acrylate ester are added in reaction kettle jointly, are improved
Reaction kettle internal temperature is stirred to react 25 minutes with 200 revs/min of rate to 100 DEG C, obtains the first reaction product;
(2)First reaction product and 16 parts of sodium lignin sulfonate, 8 parts of mutual-phenenyl two acid bromide two alcohol ester are placed in microwave treater
Microwave treatment is carried out, microwave frequency is 280 MHz, and processing time is 15 minutes, obtains treating products with microwaves;
(3)Treating products with microwaves and 8 parts of polybutylene succinate, 2 parts of alumina silicate fibre are added in mixer jointly, it will be close
Mill internal temperature is improved to 180 DEG C, at such a temperature internal mixing and plasticizing 40 minutes, and cationic antistatic agent 0.5 is then added
Part, mixer internal temperature is improved to 250 DEG C, secondary internal mixing and plasticizing 20 minutes obtains secondary mixing product and heats maintenance
In molten condition;
(4)Isooctyl acid glycidol ether is heated to molten condition for 5 parts, is added into the secondary mixing production for being similarly molten condition
Maintaining temperature in object, after being uniformly mixed keeps mixture in the range of molten state, is filled with into molten mixture
1 part of butane foaming agent, makes molten mixture fully foam;
(5)Molten mixture after foaming is injected in extruder while hot, sets extruder temperature as 150 DEG C, screw speed is
80 revs/min, extruder pressure is 50 MPa, and modified pearl cotton material is obtained after extruded, cooling, packaging.
Comparative example 3
(1)By 5 parts of talcum powder, the grinding refinement of 4 parts of mica powder, solid grain size is made to be less than 50 μm, then and low density polyethylene
150 parts of alkene, 35 parts of lauric monoglyceride, 10 parts of monomethyl polyethylene glycol acrylate ester are added in reaction kettle jointly, are improved
Reaction kettle internal temperature is stirred to react 25 minutes with 200 revs/min of rate to 100 DEG C, obtains the first reaction product;
(2)First reaction product and 16 parts of sodium lignin sulfonate, 8 parts of mutual-phenenyl two acid bromide two alcohol ester are placed in microwave treater
Microwave treatment is carried out, microwave frequency is 280 MHz, and processing time is 15 minutes, obtains treating products with microwaves;
(3)Treating products with microwaves and 8 parts of polybutylene succinate, 2 parts of alumina silicate fibre are added in mixer jointly, it will be close
Mill internal temperature is improved to 180 DEG C, at such a temperature internal mixing and plasticizing 40 minutes, and cationic antistatic agent 0.5 is then added
Part, mixer internal temperature is improved to 250 DEG C, secondary internal mixing and plasticizing 20 minutes obtains secondary mixing product and heats maintenance
In molten condition;
(4)Isopropyl three (dioctylphyrophosphoric acid acyloxy) titanate esters are mixed and heated to molten condition for 15 parts, are added into same
Sample is in the secondary mixing product of molten condition temperature to be maintained to the model for keeping mixture to be in molten state after being uniformly mixed
In enclosing, it is filled with 1 part of butane foaming agent into molten mixture, molten mixture is made fully to foam;
(5)Molten mixture after foaming is injected in extruder while hot, sets extruder temperature as 150 DEG C, screw speed is
80 revs/min, extruder pressure is 50 MPa, and modified pearl cotton material is obtained after extruded, cooling, packaging.
The modified pearl cotton material obtained of embodiment 1-3 and comparative example 1-3 is subjected to soil-burial experiment respectively, is filled
The degradation rate of material is measured after 120 days;And battery of tests is separately set, it measures and is stretched by force according to the test method of GB/T1040-2006
Degree.Test result is as shown in table 1.
Table 1
Embodiment 1 | Embodiment 2 | Embodiment 3 | Comparative example 1 | Comparative example 2 | Comparative example 3 | |
Degradation rate(%) | 15.3 | 15.6 | 15.5 | 10.7 | 11.1 | 10.9 |
Tensile strength(kg/cm2) | 3.9 | 4.0 | 4.0 | 3.8 | 3.9 | 3.9 |
The preparation method of the environment-friendly modified Pearl wool material of the present invention is by talcum powder, mica powder grinding refinement, then
It is added in reaction kettle and reacts jointly with low density polyethylene (LDPE), lauric monoglyceride, monomethyl polyethylene glycol acrylate ester, then
Reaction product and sodium lignin sulfonate, mutual-phenenyl two acid bromide two alcohol ester are subjected to microwave treatment, then by treating products with microwaves with
Polybutylene succinate, alumina silicate fibre carry out mixing twice and heat maintenance molten condition, then by three (dioctyl of isopropyl
Pyrophosphoric acid acyloxy) titanate esters, isooctyl acid glycidol ether be heated to molten condition, and it is added into and is similarly the two of molten condition
In secondary mixing product, insulation reaction simultaneously foams, and finally squeezes out while hot, is cooling, packaging, obtaining modified pearl cotton material.Prepare and
At modified pearl cotton material, still with higher tensile strength with compared with high degradability energy, as packaging
Material has a good application prospect.Also, (dioctyl is burnt present invention employs mutual-phenenyl two acid bromide two alcohol ester, isopropyl three
Phosphoric acid acyloxy) titanate esters, isooctyl acid glycidol ether participation prepare environment-friendly modified Pearl wool material, to modified pearl cotton material
Material has carried out effective performance boost, although these materials are not first Application in modified pearl cotton material, according to certain
After proportional quantity combination, it is aided with corresponding processing mode, performance is brought to the modified pearl cotton material being finally prepared
On increase substantially, this is never to report in previous research, for realize the present invention technique effect play
Conclusive effect.
Example the above is only the implementation of the present invention is not intended to limit the scope of the invention, every to utilize this hair
Equivalent structure or equivalent flow shift made by bright description is applied directly or indirectly in other relevant technology necks
Domain is included within the scope of the present invention.
Claims (6)
1. a kind of preparation method of environment-friendly modified Pearl wool material, which is characterized in that comprise the steps of:
(1)By 5~7 parts of talcum powder, the grinding refinement of 4~6 parts of mica powder, solid grain size is made to be less than 50 μm, then with it is low close
It is common to spend 150~200 parts of polyethylene, 35~45 parts of lauric monoglyceride, 10~20 parts of monomethyl polyethylene glycol acrylate ester
It is added in reaction kettle, improves reaction kettle internal temperature and be stirred reaction to 100~120 DEG C, obtain the first reaction product;
(2)First reaction product and 16~20 parts of sodium lignin sulfonate, 8~12 parts of mutual-phenenyl two acid bromide two alcohol ester are placed in microwave
Microwave treatment is carried out in processor, obtains treating products with microwaves;
(3)Treating products with microwaves and 8~10 parts of polybutylene succinate, 2~4 parts of alumina silicate fibre are added to mixer jointly
In, mixer internal temperature is improved to 180~190 DEG C, at such a temperature internal mixing and plasticizing 40~60 minutes, is then added anti-quiet
0.5~1.5 part of electric agent improves mixer internal temperature to 250 DEG C, and secondary internal mixing and plasticizing 20~30 minutes obtains secondary close
It refines product and heats and maintain molten condition;
(4)15~25 parts of isopropyl three (dioctylphyrophosphoric acid acyloxy) titanate esters, 5~9 parts of isooctyl acid glycidol ether is mixed
Conjunction is heated to molten condition, is added into the secondary mixing product for being similarly molten condition, by temperature after being uniformly mixed
It maintains and keeps mixture in the range of molten state, 1~2 part of physical blowing agent is filled with into molten mixture, keep melting mixed
Object is closed fully to foam;
(5)Molten mixture after foaming is injected in extruder while hot, sets extruder temperature as 150 DEG C, screw speed is
80~100 revs/min, extruder pressure is 50 MPa, and modified pearl cotton material is obtained after extruded, cooling, packaging.
2. the preparation method of environment-friendly modified Pearl wool material according to claim 1, which is characterized in that the step
(1)Middle mixed material is preferably stirred to react 25~35 minutes with 200~300 revs/min of rate in a kettle.
3. the preparation method of environment-friendly modified Pearl wool material according to claim 1, which is characterized in that the step
(2)The microwave frequency of middle microwave treatment is 280~300 MHz, and processing time is 15~25 minutes.
4. the preparation method of environment-friendly modified Pearl wool material according to claim 1, which is characterized in that the step
(3)In antistatic agent in cationic antistatic agent, anionic antistatic agent and non-ionic antistatic agent appoint
Meaning is a kind of.
5. the preparation method of environment-friendly modified Pearl wool material according to claim 1, which is characterized in that the step
(4)In any one in butane, hexane and carbon dioxide of physical blowing agent.
6. according to environment-friendly modified Pearl wool material made from any one of the claim 1-5 preparation methods as packaging material
Application.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810505641.0A CN108659313A (en) | 2018-05-24 | 2018-05-24 | A kind of preparation method and applications of environment-friendly modified Pearl wool material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810505641.0A CN108659313A (en) | 2018-05-24 | 2018-05-24 | A kind of preparation method and applications of environment-friendly modified Pearl wool material |
Publications (1)
Publication Number | Publication Date |
---|---|
CN108659313A true CN108659313A (en) | 2018-10-16 |
Family
ID=63777822
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201810505641.0A Withdrawn CN108659313A (en) | 2018-05-24 | 2018-05-24 | A kind of preparation method and applications of environment-friendly modified Pearl wool material |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN108659313A (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101268125A (en) * | 2005-11-04 | 2008-09-17 | 尤尼吉可株式会社 | Biodegradable resin foam sheet, biodegradable resin foam article and biodegradable resin molded container |
CN102352064A (en) * | 2011-07-06 | 2012-02-15 | 丁邦瑞 | Dual-degradant additive for promoting photo oxidative degradation and biodegradation of polymer |
CN103113651A (en) * | 2013-01-25 | 2013-05-22 | 安徽省长城汽车内饰件有限责任公司 | Method for producing high-foaming EPE pearl wool by use of carbon dioxide foaming agent |
-
2018
- 2018-05-24 CN CN201810505641.0A patent/CN108659313A/en not_active Withdrawn
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101268125A (en) * | 2005-11-04 | 2008-09-17 | 尤尼吉可株式会社 | Biodegradable resin foam sheet, biodegradable resin foam article and biodegradable resin molded container |
CN102352064A (en) * | 2011-07-06 | 2012-02-15 | 丁邦瑞 | Dual-degradant additive for promoting photo oxidative degradation and biodegradation of polymer |
CN103113651A (en) * | 2013-01-25 | 2013-05-22 | 安徽省长城汽车内饰件有限责任公司 | Method for producing high-foaming EPE pearl wool by use of carbon dioxide foaming agent |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN107629284A (en) | A kind of preparation method of antistatic foaming EPE pearl wool | |
CN109181055A (en) | Radiant crosslinked polyethylene foam and its preparation method and application | |
CN102336981A (en) | Processing modifier for polyvinyl chloride plastic-wood material | |
CN102336982A (en) | Processing modifier for polyvinyl chloride sealing strips | |
CN104327527B (en) | Wood plastic composite and preparation method thereof | |
CN105440413A (en) | Environment-friendly rich mineral paper and preparation method thereof | |
CN105255087A (en) | EPE (expandable polyethylene) bag for packing electronic products | |
CN108659313A (en) | A kind of preparation method and applications of environment-friendly modified Pearl wool material | |
CN102336979A (en) | Processing modifier for polyvinyl chloride water supply pipeline | |
CN109082135A (en) | A kind of high-strength composite packaging material and preparation method thereof | |
CN105062018A (en) | Environment-friendly plastics | |
EP2636792B1 (en) | Composition for coating cellulosic packaging material, a method of preparing composition for coating cellulosic packaging material, heat-insulating packaging material, in particular for food products, and a method for preparing heat-insulating material, in particular for food products | |
CN103980597B (en) | A kind of polyethylene foams and preparation method thereof | |
CN102775937A (en) | Preparation method of adhesive used for producing corrugated board | |
CN109609085A (en) | A kind of flame-retardant glue and preparation method thereof | |
CN108641166A (en) | Add the modified pearl cotton material preparation method and applications of polyvinylidene fluoride | |
CN108586882A (en) | Modified pearl cotton material preparation method and applications suitable for low temperature environment | |
CN108690249A (en) | A kind of thermal-insulating type modified pearl cotton material preparation method and applications | |
CN108912441A (en) | A kind of preparation method and applications of stretch-proof Pearl wool material | |
CN106189617A (en) | High temperature resistant plastic-wood material compositions and high temperature resistant mould wood and preparation method thereof | |
CN108892835A (en) | A kind of preparation method and applications of anticorrosion modified pearl cotton material | |
CN111117029A (en) | Full-degreased pearl cotton and preparation method thereof | |
CN111100354A (en) | Polyethylene heat-insulation foamed sheet and preparation method thereof | |
CN107474389A (en) | A kind of scratch-resistant, low-cost environment-friendly polypropylene material and preparation method thereof | |
CN108623882A (en) | Add the compound pearl cotton material preparation method and applications of polyglycolic acid |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
WW01 | Invention patent application withdrawn after publication | ||
WW01 | Invention patent application withdrawn after publication |
Application publication date: 20181016 |