CN109762234A - Wear resistant polyethylene plastics and preparation method - Google Patents

Wear resistant polyethylene plastics and preparation method Download PDF

Info

Publication number
CN109762234A
CN109762234A CN201910094319.8A CN201910094319A CN109762234A CN 109762234 A CN109762234 A CN 109762234A CN 201910094319 A CN201910094319 A CN 201910094319A CN 109762234 A CN109762234 A CN 109762234A
Authority
CN
China
Prior art keywords
parts
weight
stabilizer
wear
wear resistant
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.)
Pending
Application number
CN201910094319.8A
Other languages
Chinese (zh)
Inventor
李丽凤
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CN201910094319.8A priority Critical patent/CN109762234A/en
Publication of CN109762234A publication Critical patent/CN109762234A/en
Pending legal-status Critical Current

Links

Abstract

The invention belongs to technical field of polymer materials, especially wear resistant polyethylene plastics and preparation method.The application the technical solution adopted is that include following components: 150-350 parts of high density polyethylene (HDPE), 25-45 parts of ethylene-ethyl acrylate copolymer, 5-20 parts of ethene-vinyl acetate wax, 5-20 parts of nekal, 5-30 parts of methyl triacetoxysilane, 20-40 parts of white oil, 5-25 parts of anti-wear agent, 5-15 parts of stabilizer by weight.Good with wear-resisting property, color stability, and good mechanical performance, good light stability, surface smoothness is high, and the plasticity, melt flowability when melting are good, and viscosity is low, is conducive to production.

Description

Wear resistant polyethylene plastics and preparation method
Technical field
The invention belongs to technical field of polymer materials, especially wear resistant polyethylene plastics and preparation method.
Background technique
Wear resistant polyethylene has the characteristics that scratch-resistant, ageing-resistant, high-low temperature resistant, rub resistance.Be mainly used in conveyer belt, from Dynamicization equipment, conveyer guardrail, such as big C guardrail, parallel pads rail, rounded cap guardrail, flat-top guardrail, small C guardrail, plane filler strip, K-type Item is served as a contrast, Z-type serves as a contrast item etc., has the function of reducing coefficient of friction.
It prepares wear resistant polyethylene plastics needs and various auxiliary materials is added in polyethylene to significantly improve wear-resisting property.But some Auxiliary material interferes with each other, and also has various deficiencies while playing positive effect.It is therefore desirable to study a kind of wear resistant polyethylene modeling Material and preparation method.
Summary of the invention
In order to solve above-mentioned deficiency, the present invention provides wear resistant polyethylene plastics and preparation method, has wear-resisting property good, Color stability, and good mechanical performance, good light stability, surface smoothness are high.
In order to realize that goal of the invention of the invention, the present invention adopt the following technical scheme that:
A kind of wear resistant polyethylene plastics include following components: 150-350 parts of high density polyethylene (HDPE), ethylene-the third by weight 25-45 parts of olefin(e) acid methacrylate copolymers, 5-20 parts of ethene-vinyl acetate wax, 5-20 parts of nekal, methyl triacetyl oxygen 5-30 parts of base silane, 20-40 parts of white oil, 5-25 parts of anti-wear agent, 5-15 parts of stabilizer.
Further, the anti-wear agent is by weight are as follows: 5-15 parts of Algisium C, trimethyl silicane 3-12 parts of sodium alkoxide;
Further, the stabilizer is by weight: 5~25 parts of dimethylamido sodium, furfuryl thiopropionate 5~30 Part.
A kind of preparation method of above-mentioned wear resistant polyethylene plastics is:
(1) high density polyethylene (HDPE), ethylene-ethyl acrylate copolymer, ethene-vinyl acetate wax, dibutyl naphthalene sulphur are weighed Sour sodium, methyl triacetoxysilane, white oil, anti-wear agent, add to a three-leaf mixe, at a temperature of mixing condition is 75-95 DEG C Mixing 0.5-1 hours is uniformly mixed;
(2) it by the product of step 1 in high pressure homogenizer, at 70-90 DEG C, mixes 10 minutes, temperature adjustment adds to 75-85 DEG C Enter stabilizer homogeneous 10 minutes, carries out deaeration 1-4 hours under vacuum conditions, the raw material mixed;
(3) by the feedstock transportation mixed, into plastic extruder, extruding pelletization, control screw speed are 170-320r/ min;Temperature is 160-250 DEG C, obtains wear resistant polyethylene plastics of the invention.
Methyl triacetoxysilane can get up polyethylene and the coupling of auxiliary material interface, to improve the property of material It can and increase bond strength.Inventor has found that the coupling effect of methyl triacetoxysilane can be enhanced in nekal Fruit, but its coupling effect is unstable, viscosity is very big when will lead to melting when it is shared, and melt flow rate (MFR) significantly drops Low, lane shear rate is also extremely low, therefore, it is difficult to be processed and guaranteed the performance of material, it is therefore desirable to continue to study. Inventor has found that pass through at the same Algisium C is added, trimethyl silicane sodium alkoxide can be to high density Polyethylene, ethylene-ethyl acrylate copolymer are modified, while stablizing nekal and methyl triacetoxyl group silicon Thermally sensitive coupling effect when alkane shares, the two mutually play synergistic effect, improve plasticity when composition melting And viscosity and melt flowability improve speed of production to reduce the difficulty of processing, can not only improve material and add Work mechanical strength performance after molding, and since coupling effect is stablized, the performance of each component can have been fully played, has had plastics There is splendid wear-resisting property to have both the effect of corrosion resistance.And if being only individually added into trimethyl silicane sodium alkoxide instead to the whole of material The improvement of body fluidity of molten is unsatisfactory, moreover, the mechanical strength performance for product also decreases, therefore, the two is necessary It exists simultaneously, just can guarantee the overall performance of material.
Ageing process is mainly photooxidation resistance and thermo-oxidative ageing, is radical reaction course.The said effect of anti-wear agent is true The performance of real but resistance to photooxidation resistance is not ideal enough, and generation radical chain reaction is easily led under the conditions of photooxidation.Therefore it develops steady Agent is determined for terminating radical chain reaction caused by anti-wear agent, and reaction generates unsaturated intermediate as nitrogen oxygen under Photooxidation Conditions The depots of free radical prevent polyethylene long-chain from being broken.Therefore, vinyon provided by the present application can be resistant to sunlight, purple Outside line irradiation, is not easy coarse, aging, colour fading, photostability is more preferable.
The utility model has the advantages that 1: the present invention stabilizes nekal and when methyl triacetoxysilane shares to temperature Sensitive coupling effect makes wear resistant polyethylene have good plasticity, viscosity and fluidity of molten in melting, and when stirring cuts Shear force is small, is easy to generate processing, extruded velocity is fast, and product surface is smooth.
Color stability.
2: since coupling effect is stablized, the performance of each component can have been fully played, made plastics that there is splendid wearability It can and have both the effect of corrosion resistance.
3: sunlight, ultraviolet light irradiation can be resistant to, be not easy coarse, aging, colour fading, photostability is more preferable.
4: anti-wear agent keeps the extrusion performance of vinyon more preferable, and product surface is not likely to produce cold spot, the line that becomes, crazing, gas Phenomena such as steeping flow liner or rough surface.
Specific embodiment
Technical solution of the present invention is described in further detail combined with specific embodiments below, but the present invention is not limited to following Embodiment.Unless otherwise indicated, various components used in the present invention are this field current material, can be purchased by commercial channel It buys acquisition or is made by existing method.
Embodiment 1
A kind of wear resistant polyethylene plastics include following components: 160 parts of high density polyethylene (HDPE), ethylene-acrylic acid by weight It is 40 parts of methacrylate copolymers, 6 parts of ethene-vinyl acetate wax, 17 parts of nekal, 7 parts of methyl triacetoxysilane, white Oily 35 parts, 6 parts of anti-wear agent, 13 parts of stabilizer;
Further, the anti-wear agent is by weight are as follows: 6 parts of Algisium C, trimethyl silanol 10 parts of sodium;
Further, the stabilizer is by weight: 8 parts of dimethylamido sodium, 25 parts of furfuryl thiopropionate;
A kind of preparation method of above-mentioned wear resistant polyethylene plastics is:
(1) high density polyethylene (HDPE), ethylene-ethyl acrylate copolymer, ethene-vinyl acetate wax, dibutyl naphthalene sulphur are weighed Sour sodium, methyl triacetoxysilane, white oil, anti-wear agent, add to a three-leaf mixe, and mixing condition mixes at a temperature of being 78 DEG C It 0.8 hour, is uniformly mixed;
(2) it by the product of step 1 in high pressure homogenizer, at 75 DEG C, mixes 10 minutes, temperature adjustment is added and stablizes to 75 DEG C It agent homogeneous 10 minutes, carries out deaeration 1.5 hours under vacuum conditions, the raw material mixed;
(3) by the feedstock transportation mixed, into plastic extruder, extruding pelletization, control screw speed are 190r/min; Temperature is 180 DEG C, obtains wear resistant polyethylene plastics of the invention.
Embodiment 2
A kind of wear resistant polyethylene plastics include following components: 320 parts of high density polyethylene (HDPE), ethylene-acrylic acid by weight 30 parts of methacrylate copolymers, 18 parts of ethene-vinyl acetate wax, 6 parts of nekal, 25 parts of methyl triacetoxysilane, 22 parts of white oil, 22 parts of anti-wear agent, 7 parts of stabilizer;
Further, the anti-wear agent is by weight are as follows: 13 parts of Algisium C, trimethyl silanol 5 parts of sodium;
Further, the stabilizer is by weight: 19 parts of dimethylamido sodium, 7 parts of furfuryl thiopropionate;
A kind of preparation method of above-mentioned wear resistant polyethylene plastics is:
(1) high density polyethylene (HDPE), ethylene-ethyl acrylate copolymer, ethene-vinyl acetate wax, dibutyl naphthalene sulphur are weighed Sour sodium, methyl triacetoxysilane, white oil, anti-wear agent, add to a three-leaf mixe, and mixing condition mixes at a temperature of being 92 DEG C It 1 hour, is uniformly mixed;
(2) it by the product of step 1 in high pressure homogenizer, at 88 DEG C, mixes 10 minutes, temperature adjustment is added and stablizes to 84 DEG C It agent homogeneous 10 minutes, carries out deaeration 3.5 hours under vacuum conditions, the raw material mixed;
(3) by the feedstock transportation mixed, into plastic extruder, extruding pelletization, control screw speed are 310r/min; Temperature is 240 DEG C, obtains wear resistant polyethylene plastics of the invention.
Embodiment 3
A kind of wear resistant polyethylene plastics include following components: 250 parts of high density polyethylene (HDPE), ethylene-acrylic acid by weight 30 parts of methacrylate copolymers, 13 parts of ethene-vinyl acetate wax, 12 parts of nekal, 17 parts of methyl triacetoxysilane, 30 parts of white oil, 15 parts of anti-wear agent, 20 parts of stabilizer;
Further, the anti-wear agent is by weight are as follows: 10 parts of Algisium C, trimethyl silanol 8 parts of sodium;
Further, the stabilizer is by weight: 15 parts of dimethylamido sodium, 17 parts of furfuryl thiopropionate;
A kind of preparation method of above-mentioned wear resistant polyethylene plastics is:
(1) high density polyethylene (HDPE), ethylene-ethyl acrylate copolymer, ethene-vinyl acetate wax, dibutyl naphthalene sulphur are weighed Sour sodium, methyl triacetoxysilane, white oil, anti-wear agent, add to a three-leaf mixe, and mixing condition mixes at a temperature of being 80 DEG C It 0.7 hour, is uniformly mixed;
(2) it by the product of step 1 in high pressure homogenizer, at 75 DEG C, mixes 10 minutes, temperature adjustment is added and stablizes to 80 DEG C It agent homogeneous 10 minutes, carries out deaeration 2.5 hours under vacuum conditions, the raw material mixed;
(3) by the feedstock transportation mixed, into plastic extruder, extruding pelletization, control screw speed are 240r/min; Temperature is 205 DEG C, obtains wear resistant polyethylene plastics of the invention.
Embodiment 4
A kind of wear resistant polyethylene plastics include following components: 300 parts of high density polyethylene (HDPE), ethylene-acrylic acid by weight 40 parts of methacrylate copolymers, 18 parts of ethene-vinyl acetate wax, 15 parts of nekal, 25 parts of methyl triacetoxysilane, 30 parts of white oil, 23 parts of anti-wear agent, 12 parts of stabilizer;
Further, the anti-wear agent is by weight are as follows: 12 parts of Algisium C, trimethyl silanol 7 parts of sodium;
Further, the stabilizer is by weight: 9 parts of dimethylamido sodium, 15 parts of furfuryl thiopropionate;
A kind of preparation method of above-mentioned wear resistant polyethylene plastics is:
(1) high density polyethylene (HDPE), ethylene-ethyl acrylate copolymer, ethene-vinyl acetate wax, dibutyl naphthalene sulphur are weighed Sour sodium, methyl triacetoxysilane, white oil, anti-wear agent, add to a three-leaf mixe, and mixing condition mixes at a temperature of being 90 DEG C It 0.5 hour, is uniformly mixed;
(2) it by the product of step 1 in high pressure homogenizer, at 85 DEG C, mixes 10 minutes, temperature adjustment is added and stablizes to 80 DEG C It agent homogeneous 10 minutes, carries out deaeration 2 hours under vacuum conditions, the raw material mixed;
(3) by the feedstock transportation mixed, into plastic extruder, extruding pelletization, control screw speed are 170-320r/ min;Temperature is 160-250 DEG C, obtains wear resistant polyethylene plastics of the invention.
Comparative example 1: the difference of comparative example 1 and embodiment 3 is without containing Algisium C, remaining Condition is all the same.
Comparative example 2: the difference of comparative example 2 and embodiment 3 is that, without containing trimethyl silicane sodium alkoxide, remaining condition is homogeneous Together.
Comparative example 3: the difference of comparative example 3 and embodiment 3 is without containing anti-wear agent provided by the present application, remaining condition It is all the same.
Comparative test 1: by wear-resistant plastic made from above-described embodiment 1-4 and comparative example 1-3, being molded and template be made, warp Test properties are as follows:
Table 1
Wearability is worn with volume to be characterized, and is surveyed according to GB/T 3960-2016 plastic slide friction wear test method Examination;
MI (g/10min), it indicates the grams that the plastics are extruded in 10 minutes.MI is bigger, represents the plastic raw materials Viscosity is smaller and molecular wt is smaller, on the contrary then represent that the plastic viscosity is bigger and molecular wt is bigger.
In impact strength test: C is that fracture --- sample is divided into the fracture of two sections or multistage completely.
H is hinge break --- it is a kind of incomplete fracture, a part of sample cannot make selve support in level Position, and another part still keeps vertical (angle is less than 90 ° between two parts).(two sections of rupture test specimen are only by very thin table Skin links together, and this hinge does not have any residual rigidity.
P is portion fractures --- and a kind of not exclusively fracture, but do not meet hinge fracture definition, but dent wedge angle extremely Crackle at least 90% between another side.
NB is non-fracture --- it is a kind of not exclusively fracture, does not reach in dent wedge angle to the crack propagation between another side 90%.(only curved, may to there is the generation of stress whitening phenomenon).
Acid dip test, according to CNS10757 (1995) standard test;Oil resisting test is marked according to CNS10757 (1995) Quasi- measurement.
Anti-wear agent known to comparative example 1-4 and comparative example 1-3 can improve the plasticity and viscosity when composition melting And melt flowability, the difficulty of processing is reduced, speed of production is improved, the mechanics after can not only improving material machine-shaping is strong Performance and surface smoothness are spent, and since coupling effect is stablized, the performance of each component can have been fully played, made plastics that there is pole Good wear-resisting property has both the effect of corrosion resistance.
Comparative experiments 2: ageing properties detection
Comparative example 4: the difference of comparative example 4 and embodiment 3 is that, without containing dimethylamido sodium, remaining condition is homogeneous Together.
Comparative example 5: the difference of comparative example 5 and embodiment 3 is that, without containing furfuryl thiopropionate, remaining condition is homogeneous Together.
Comparative example 6: the difference of comparative example 6 and embodiment 3 is without containing stabilizer provided by the present application, remaining condition It is all the same.
Ageing properties detection is carried out according to the examination criteria of national standard GB/T 3681-2011, testing result is as shown in the table:
Table 2
Comparative example 4-6 wearability after degradation, which largely reduces, illustrates plastic material aging, polyethylene long-chain easy fracture Cause to fall off.
Embodiment 1-4 and comparative example 4-6 is compared it is found that stabilizer can prevent anti-wear agent from causing to occur under the conditions of photooxidation Radical chain reaction, so that polyethylene long-chain be prevented to be broken.Therefore, vinyon provided by the present application can be resistant to sunlight, Ultraviolet light irradiation, is not easy coarse, aging, colour fading, photostability is more preferable, and mechanical property is more stable.
The above is only the preferred embodiment of the present invention, it is noted that above-mentioned preferred embodiment is not construed as pair Limitation of the invention, protection scope of the present invention should be defined by the scope defined by the claims..For the art For those of ordinary skill, without departing from the spirit and scope of the present invention, several improvements and modifications can also be made, these change It also should be regarded as protection scope of the present invention into retouching.

Claims (10)

1. a kind of wear resistant polyethylene plastics, it is characterised in that by weight include following components: high density polyethylene (HDPE) 150-350 Part, 25-45 parts of ethylene-ethyl acrylate copolymer, 5-20 parts of ethene-vinyl acetate wax, 5-20 parts of nekal, first 5-30 parts of base triacetoxysilane, 20-40 parts of white oil, 5-25 parts of anti-wear agent, 5-15 parts of stabilizer.
2. a kind of wear resistant polyethylene plastics according to claim 1, it is characterized in that the anti-wear agent is by weight are as follows: first 5-15 parts, 3-12 parts of trimethyl silicane sodium alkoxide of base silane alcohol mannuronic acid ester.
3. according to claim 1, a kind of wear resistant polyethylene plastics described in 2, it is characterized in that the stabilizer is by weight: two 5~25 parts of formamido group sodium, 5~30 parts of furfuryl thiopropionate.
4. a kind of wear resistant polyethylene plastics according to claim 1 to 3, it is characterized in that by weight including following components: high 150-350 parts of density polyethylene, 25-45 parts of ethylene-ethyl acrylate copolymer, 5-20 parts of ethene-vinyl acetate wax, dibutyl 5-20 parts of sodium naphthalene sulfonate, 5-30 parts of methyl triacetoxysilane, 20-40 parts of white oil, 5-25 parts of anti-wear agent, stabilizer 5-15 Part;
The anti-wear agent is by weight are as follows: 5-15 parts of Algisium C, 3-12 parts of trimethyl silicane sodium alkoxide.
5. a kind of wear resistant polyethylene plastics according to claim 1 to 3, it is characterized in that by weight including following components: high 150-350 parts of density polyethylene, 25-45 parts of ethylene-ethyl acrylate copolymer, 5-20 parts of ethene-vinyl acetate wax, dibutyl 5-20 parts of sodium naphthalene sulfonate, 5-30 parts of methyl triacetoxysilane, 20-40 parts of white oil, 5-25 parts of anti-wear agent, stabilizer 5-15 Part;
The stabilizer is by weight: 5~25 parts of dimethylamido sodium, 5~30 parts of furfuryl thiopropionate.
6. a kind of wear resistant polyethylene plastics described in -4 according to claim 1, it is characterized in that being by weight following components: highly dense Spend polyethylene 150-350 parts, 25-45 parts of ethylene-ethyl acrylate copolymer, 5-20 parts of ethene-vinyl acetate wax, dibutyl naphthalene 5-20 parts of sodium sulfonate, 5-30 parts of methyl triacetoxysilane, 20-40 parts of white oil, 5-25 parts of anti-wear agent, 5-15 parts of stabilizer;
The anti-wear agent is by weight are as follows: 5-15 parts of Algisium C, 3-12 parts of trimethyl silicane sodium alkoxide;
The stabilizer is by weight: 5~25 parts of dimethylamido sodium, 5~30 parts of furfuryl thiopropionate.
7. a kind of preparation method of wear resistant polyethylene plastics described in -6 according to claim 1, characterized in that
(1) weigh high density polyethylene (HDPE), ethylene-ethyl acrylate copolymer, ethene-vinyl acetate wax, nekal, Methyl triacetoxysilane, white oil, anti-wear agent, add to a three-leaf mixe, and mixing condition mixes at a temperature of being 75-95 DEG C It 0.5-1 hours, is uniformly mixed;
(2) it by the product of step 1 in high pressure homogenizer, at 70-90 DEG C, mixes 10 minutes, temperature adjustment is added steady to 75-85 DEG C Determine agent homogeneous 10 minutes, carries out deaeration 1-4 hours under vacuum conditions, the raw material mixed;
(3) by the feedstock transportation mixed, into plastic extruder, extruding pelletization, control screw speed are 170-320r/min; Temperature is 160-250 DEG C, obtains wear resistant polyethylene plastics of the invention.
8. a kind of wear resistant polyethylene plastics described in -7 according to claim 1, it is characterized in that: being by weight following components: high 150-350 parts of density polyethylene, 25-45 parts of ethylene-ethyl acrylate copolymer, 5-20 parts of ethene-vinyl acetate wax, dibutyl 5-20 parts of sodium naphthalene sulfonate, 5-30 parts of methyl triacetoxysilane, 20-40 parts of white oil, 5-25 parts of anti-wear agent, stabilizer 5-15 Part;
The anti-wear agent is by weight are as follows: 5-15 parts of Algisium C, 3-12 parts of trimethyl silicane sodium alkoxide;
The stabilizer is by weight: 5~25 parts of dimethylamido sodium, 5~30 parts of furfuryl thiopropionate;
Preparation method is that (1) weighs high density polyethylene (HDPE), ethylene-ethyl acrylate copolymer, ethene-vinyl acetate wax, two fourths Base sodium naphthalene sulfonate, methyl triacetoxysilane, white oil, anti-wear agent, add to a three-leaf mixe, and mixing condition is 75-95 DEG C At a temperature of mix 0.5-1 hours, be uniformly mixed;
(2) it by the product of step 1 in high pressure homogenizer, at 70-90 DEG C, mixes 10 minutes, temperature adjustment is added steady to 75-85 DEG C Determine agent homogeneous 10 minutes, carries out deaeration 1-4 hours under vacuum conditions, the raw material mixed;
(3) by the feedstock transportation mixed, into plastic extruder, extruding pelletization, control screw speed are 170-320r/min; Temperature is 160-250 DEG C, obtains wear resistant polyethylene plastics of the invention.
9. a kind of wear resistant polyethylene plastics described in -8 according to claim 1, it is characterized in that: being by weight following components: high 160 parts of density polyethylene, 40 parts of ethylene-ethyl acrylate copolymer, 6 parts of ethene-vinyl acetate wax, nekal 17 Part, 7 parts of methyl triacetoxysilane, 35 parts of white oil, 6 parts of anti-wear agent, 13 parts of stabilizer;
Further, the anti-wear agent is by weight are as follows: 6 parts of Algisium C, trimethyl silicane sodium alkoxide 10 Part;
Further, the stabilizer is by weight: 8 parts of dimethylamido sodium, 25 parts of furfuryl thiopropionate;
A kind of preparation method of above-mentioned wear resistant polyethylene plastics is:
(1) weigh high density polyethylene (HDPE), ethylene-ethyl acrylate copolymer, ethene-vinyl acetate wax, nekal, Methyl triacetoxysilane, white oil, anti-wear agent, add to a three-leaf mixe, and mixing 0.8 is small at a temperature of mixing condition is 78 DEG C When, it is uniformly mixed;
(2) it by the product of step 1 in high pressure homogenizer, at 75 DEG C, mixes 10 minutes, it is equal that stabilizer is added to 75 DEG C in temperature adjustment It matter 10 minutes, carries out deaeration 1.5 hours under vacuum conditions, the raw material mixed;
(3) by the feedstock transportation mixed, into plastic extruder, extruding pelletization, control screw speed are 190r/min;Temperature It is 180 DEG C, obtains wear resistant polyethylene plastics of the invention.
10. a kind of wear resistant polyethylene plastics described in -8 according to claim 1, it is characterized in that: by weight including following components: 320 parts of high density polyethylene (HDPE), 30 parts of ethylene-ethyl acrylate copolymer, 18 parts of ethene-vinyl acetate wax, dibutyl naphthalenesulfonic acid 6 parts of sodium, 25 parts of methyl triacetoxysilane, 22 parts of white oil, 22 parts of anti-wear agent, 7 parts of stabilizer;
Further, the anti-wear agent is by weight are as follows: 13 parts of Algisium C, trimethyl silicane sodium alkoxide 5 Part;
Further, the stabilizer is by weight: 19 parts of dimethylamido sodium, 7 parts of furfuryl thiopropionate;
A kind of preparation method of above-mentioned wear resistant polyethylene plastics is:
(1) weigh high density polyethylene (HDPE), ethylene-ethyl acrylate copolymer, ethene-vinyl acetate wax, nekal, Methyl triacetoxysilane, white oil, anti-wear agent, add to a three-leaf mixe, and mixing 1 is small at a temperature of mixing condition is 92 DEG C When, it is uniformly mixed;
(2) it by the product of step 1 in high pressure homogenizer, at 88 DEG C, mixes 10 minutes, it is equal that stabilizer is added to 84 DEG C in temperature adjustment It matter 10 minutes, carries out deaeration 3.5 hours under vacuum conditions, the raw material mixed;
(3) by the feedstock transportation mixed, into plastic extruder, extruding pelletization, control screw speed are 310r/min;Temperature It is 240 DEG C, obtains wear resistant polyethylene plastics of the invention.
CN201910094319.8A 2019-01-30 2019-01-30 Wear resistant polyethylene plastics and preparation method Pending CN109762234A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910094319.8A CN109762234A (en) 2019-01-30 2019-01-30 Wear resistant polyethylene plastics and preparation method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910094319.8A CN109762234A (en) 2019-01-30 2019-01-30 Wear resistant polyethylene plastics and preparation method

Publications (1)

Publication Number Publication Date
CN109762234A true CN109762234A (en) 2019-05-17

Family

ID=66454522

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910094319.8A Pending CN109762234A (en) 2019-01-30 2019-01-30 Wear resistant polyethylene plastics and preparation method

Country Status (1)

Country Link
CN (1) CN109762234A (en)

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1624038A (en) * 2003-12-02 2005-06-08 上海高分子功能材料研究所 Room-temp, silane cross linked polyethylene plastic and its preparation method
CN105037899A (en) * 2015-09-02 2015-11-11 国网山东莒南县供电公司 Low-smoke halogen-free flame-retardant cable material
CN105199187A (en) * 2014-11-11 2015-12-30 无锡工艺职业技术学院 Low-energy-consumption, high-flame-retardancy, low-smoke and halogen-free cable material
CN106009226A (en) * 2016-07-08 2016-10-12 浙江太湖远大新材料股份有限公司 Organosilane crosslinked polyethylene wires and cables of 10 kV or below and preparation method thereof
CN106046491A (en) * 2016-07-02 2016-10-26 苏州横远微控技术有限公司 PE-based composite material as well as preparation method and application thereof
CN106947148A (en) * 2017-05-03 2017-07-14 马志明 A kind of anti-aging wear-resisting PE plastic pipes
CN106947144A (en) * 2017-04-18 2017-07-14 苏州海凌达电子科技有限公司 A kind of wear-resisting PE plastic pipes of antibacterial

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1624038A (en) * 2003-12-02 2005-06-08 上海高分子功能材料研究所 Room-temp, silane cross linked polyethylene plastic and its preparation method
CN105199187A (en) * 2014-11-11 2015-12-30 无锡工艺职业技术学院 Low-energy-consumption, high-flame-retardancy, low-smoke and halogen-free cable material
CN105037899A (en) * 2015-09-02 2015-11-11 国网山东莒南县供电公司 Low-smoke halogen-free flame-retardant cable material
CN106046491A (en) * 2016-07-02 2016-10-26 苏州横远微控技术有限公司 PE-based composite material as well as preparation method and application thereof
CN106009226A (en) * 2016-07-08 2016-10-12 浙江太湖远大新材料股份有限公司 Organosilane crosslinked polyethylene wires and cables of 10 kV or below and preparation method thereof
CN106947144A (en) * 2017-04-18 2017-07-14 苏州海凌达电子科技有限公司 A kind of wear-resisting PE plastic pipes of antibacterial
CN106947148A (en) * 2017-05-03 2017-07-14 马志明 A kind of anti-aging wear-resisting PE plastic pipes

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
刘奎武: "《管道施工理论与实际操作集成》", 31 August 2017, 北京:冶金工业出版社 *
卢少忠 等: "《塑料管道工程性能.生产.应用》", 30 June 2004, 中国建材工业出版社 *
温辉梁主编: "《化工助剂》", 31 December 2009, 南昌:江西科学技术出版社 *
许戈文主编: "《合成香料产品技术手册》", 28 February 1996, 北京:中国商业出版社 *

Similar Documents

Publication Publication Date Title
CN107266894B (en) Poly carbonate resin composition and molded article for optical use
CN107189395B (en) A kind of glass fibre reinforced poly carbonate composite and preparation method thereof
US20200148876A1 (en) Ultralow-glossiness, ultralow-temperature resistant asa resin composition and preparation method thereof
JPH0270737A (en) Extrudable thermoplastic hydrocarbon polymer composition
US6900266B2 (en) Method of compounding a multimodal polyethylene composition
CN106674712B (en) A kind of anti stick low-smoke non-halogen flame-retardant protecting sleeve of optical cable and preparation method thereof
US9346704B2 (en) Optical glass
CN109337272A (en) A kind of PMMA/ASA alloy resin composition and preparation method thereof
CN105255072A (en) Rubber cable sheathing material resistant to high and low temperature
JP3177984B2 (en) Polyoxymethylene compositions containing at least one encapsulated nucleating agent
CN109762234A (en) Wear resistant polyethylene plastics and preparation method
CN106398234B (en) A kind of Halogenless flaming retarding cold resistant PC material and preparation method thereof suitable for charging pile charging gun
CN104031303B (en) Polyethylene master batch compound additive and preparation method thereof
CN111909473B (en) Extremely low-precipitation high-elasticity PVC glove composition and method for preparing gloves
CN112920506A (en) High-performance scratch-resistant polypropylene composite material and preparation method thereof
JP4084887B2 (en) Composition based on polyethylene and method for producing shaped article of the composition
CN109749206A (en) A kind of polyethylene color master batch and preparation method thereof
WO2020147684A1 (en) Polycarbonate composition and preparation method therefor
CN105623060B (en) A kind of polyethylene composition and its film
CN105111629A (en) High-resistance PVC alloy profile and preparation method thereof
WO2022222536A1 (en) Low shrinkage polyethylene sheath material, preparation method therefor and application thereof
CN111117201B (en) High-hardness PC (polycarbonate) photodiffusion material and preparation method thereof
CN108047677A (en) A kind of high-wear-resistancehigh-strength high-strength polycarbonate composite material and preparation method thereof
CN108239321A (en) A kind of preparation method of bridge cable special sheath material
CN110982161A (en) Special PE sheath material for photoelectricity

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
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20190517