CN109135008B - Filling master batch, preparation method and application thereof, and polypropylene wiredrawing material containing filling master batch - Google Patents
Filling master batch, preparation method and application thereof, and polypropylene wiredrawing material containing filling master batch Download PDFInfo
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/20—Compounding polymers with additives, e.g. colouring
- C08J3/22—Compounding polymers with additives, e.g. colouring using masterbatch techniques
- C08J3/226—Compounding polymers with additives, e.g. colouring using masterbatch techniques using a polymer as a carrier
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/44—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds
- D01F6/46—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds of polyolefins
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- 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
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- C08J2423/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2423/02—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
- C08J2423/04—Homopolymers or copolymers of ethene
- C08J2423/06—Polyethene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2423/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2423/02—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
- C08J2423/10—Homopolymers or copolymers of propene
- C08J2423/12—Polypropene
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Abstract
The invention provides a filling master batch, a preparation method and application thereof, and a polypropylene wiredrawing material containing the filling master batch. The filling master batch comprises the following components in percentage by weight: 75-88% of filler, 0.5-2% of coupling agent, 5-20% of low-melting-index polyethylene, 3-10% of high-melting-index polyethylene and 2-5% of polypropylene wax. The filling master batch is prepared by mixing and reacting the filler and the coupling agent, then mixing the mixture with other components and extruding the mixture. The filling master batch provided by the invention has good high temperature resistance, can be used as a filling master batch of a polypropylene wire drawing material, and improves the mechanical property of the polypropylene wire drawing material and the fuming problem in the production process of polypropylene wire drawing.
Description
Technical Field
The invention belongs to the technical field of polypropylene drawing, and particularly relates to a filling master batch, a preparation method and application thereof, and a polypropylene drawing material containing the filling master batch.
Background
The polypropylene wiredrawing material is a common raw material of a plastic woven product, has excellent tensile property, and has the characteristics of no water absorption, corrosion resistance, no mildew, wear resistance, long service life and the like. In addition, the polypropylene wiredrawing material can also be used for producing color strip cloth, carpet backing (base cloth), flexible freight bags, tarpaulins and ropes.
The polypropylene wire drawing material mainly comprises polypropylene resin, filling master batch and auxiliary agent, wherein the commonly used filling master batch of the polypropylene wire drawing material is calcium carbonate filling master batch, and the calcium carbonate filling master batch is used for reducing the cost on one hand and improving the mechanical strength of polypropylene wire drawing on the other hand. In consideration of the influence of the filling master batch on the drawing mechanical property of polypropylene, high molecular weight polyethylene or polypropylene (with a melt index of about 2g/10 min) is generally used as a matrix resin, and because of the low melt flow rate, the processing needs to be added with a large amount of auxiliaries such as paraffin, stearic acid and the like so as to improve the processing fluidity of the filling master batch. However, in the polypropylene drawing process, the processing temperature is as high as 260 ℃, and auxiliaries such as paraffin, stearic acid and the like are decomposed and fuming at the temperature, so that a large amount of smoke is generated, and the environment and the health of workers are greatly influenced.
For example, CN 1935889a discloses a special material for polypropylene woven bag wire drawing, which comprises polypropylene resin, calcium carbonate, 168 antioxidant, BC1010 antioxidant, calcium stearate, stearic acid, special modifier and white oligomer sheet. CN 1966562A discloses a filling master batch for polypropylene drawing, which comprises superfine calcium carbonate, superfine talcum powder, homo-polypropylene, ethylene propylene rubber, ethylene-vinyl acetate copolymer wax, stearic acid and zinc stearate. Both use stearic acid to improve flow, which also entails fuming during drawing.
Therefore, how to improve the defect of fuming in the drawing process on the premise of ensuring the processing fluidity and the mechanical property of the polypropylene drawing material is a problem to be solved in the field.
Disclosure of Invention
Aiming at the defects in the prior art, the invention aims to provide a filling master batch, a preparation method and application thereof and a polypropylene wiredrawing material containing the filling master batch. The filling master batch has good high temperature resistance, improves the mechanical property of the polypropylene wire drawing machine, and simultaneously improves the fuming problem in the production process of polypropylene wire drawing.
In order to achieve the purpose, the invention adopts the following technical scheme:
in a first aspect, the invention provides a filling master batch, which comprises the following components in percentage by weight:
the low-melt index polyethylene has a melt index of 0.01-2g/10min, and the high-melt index polyethylene has a melt index of 20-40g/10 min.
The invention adopts two polyethylene and polypropylene wax with different melt indexes to match and replace a low-melt-index polyethylene/polypropylene, paraffin and stearic acid system, and the obtained filling master batch can meet the fluidity requirement of a wire drawing process. Because the filling master batch does not contain auxiliary agents with lower decomposition temperature such as paraffin, stearic acid and the like, the adverse effect of the auxiliary agents on the mechanical property is avoided, so the filling master batch provided by the invention cannot be fuming in the drawing process and has good mechanical property.
In the present invention, the weight percentage of the filler may be 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, or the like.
The weight percentage of the coupling agent may be 0.5%, 0.6%, 0.7%, 0.8%, 0.9%, 1%, 1.1%, 1.2%, 1.3%, 1.4%, 1.5%, 1.6%, 1.7%, 1.8%, 1.9%, 2%, or the like.
By low melt it is meant that the weight percentage of polyethylene may be 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, or the like.
The high melt index polyethylene may be 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, or the like, by weight.
The polypropylene wax may be present in an amount of 2%, 2.5%, 3%, 3.5%, 4%, 4.5%, 5%, or the like.
As a preferred technical scheme of the invention, the filler is selected from one or a combination of at least two of calcium carbonate, kaolin, silica or wollastonite; typical but non-limiting examples of such combinations are: combinations of calcium carbonate and kaolin, calcium carbonate and wollastonite, kaolin and silica, kaolin and wollastonite, silica and wollastonite, and the like.
Preferably, the particle size of the filler is 2-20 μm; for example, it may be 2 μm, 4 μm, 5 μm, 8 μm, 10 μm, 12 μm, 15 μm, 18 μm or 20 μm.
As a preferred technical scheme of the invention, the coupling agent is a titanate coupling agent and/or a silane coupling agent.
Preferably, the titanate coupling agent is selected from one or a combination of at least two of isopropyl tris (dioctyl pyrophosphato) titanate (TMC-201), isopropyl dioleato acyloxy (dioctyl phosphato) titanate (TMC-101), isopropyl triisostearoyl titanate or isopropyl distearoyl methacryloyl titanate.
Preferably, the silane coupling agent is selected from one or a combination of at least two of gamma-aminopropyltriethoxysilane (KH-550), gamma- (2, 3-glycidoxy) propyltrimethoxysilane (KH-560), vinyltriethoxysilane (A-151) or gamma-methacrylate trimethoxysilane.
As a preferred embodiment of the present invention, the filling masterbatch further comprises 0.5 to 1 wt% (e.g., may be 0.5 wt%, 0.6 wt%, 0.7 wt%, 0.8 wt%, 0.9 wt%, or 1 wt%, etc.) of a lubricant.
The lubricant is helpful for further improving the fluidity of the filling master batch and improving the processing performance.
Preferably, the lubricant is ethylene bisstearamide and/or pentaerythritol tetrastearate.
In a second aspect, the present invention provides a method for preparing the filling masterbatch, which comprises the following steps:
(1) mixing and reacting a filler and a coupling agent to obtain a modified filler;
(2) mixing the modified filler obtained in the step (1) with the rest of components;
(3) extruding the mixed material obtained in the step (2) through an extruder to obtain the filling master batch.
As a preferred embodiment of the present invention, the preparation method further comprises: drying the filler prior to said mixing in step (1).
The purpose of drying is to prevent the coupling agent from reacting with the moisture in the filler and becoming ineffective.
Preferably, the drying method comprises the following steps: the filler is added into a high-speed mixer, heated to 120 ℃ (for example, 110 ℃, 111 ℃, 112 ℃, 113 ℃, 114 ℃, 115 ℃, 116 ℃, 117 ℃, 118 ℃, 119 ℃ or 120 ℃, and the like), and stirred for 5-10min (for example, 5min, 5.5min, 6min, 6.5min, 7min, 7.5min, 8min, 8.5min, 9min, 9.5min or 10min, and the like) at the rotation speed of 1200-1480r/min (for example, 1200r/min, 1250r/min, 1300r/min, 1350r/min, 1400r/min, 1450r/min or 1480r/min and the like).
Preferably, the mixing in step (1) and step (2) is carried out in a high mixing machine.
Preferably, the mixing speed in step (1) is 1200-1480r/min, such as 1200r/min, 1250r/min, 1300r/min, 1350r/min, 1400r/min, 1450r/min or 1480 r/min; the time is 4-6min, such as 4min, 4.2min, 4.5min, 4.8min, 5min, 5.2min, 5.5min, 5.8min or 6 min.
Preferably, the mixing speed in step (2) is 1200-1480r/min, such as 1200r/min, 1250r/min, 1300r/min, 1350r/min, 1400r/min, 1450r/min or 1480 r/min; the time is 5-10min, such as 5min, 5.5min, 6min, 6.5min, 7min, 7.5min, 8min, 8.5min, 9min, 9.5min or 10 min.
Preferably, the extruder in step (3) is a twin-screw extruder.
Preferably, the head temperature of the twin-screw extruder is 150-; the temperature of the extrusion section is 150 ℃ to 180 ℃, and may be, for example, 150 ℃, 152 ℃, 155 ℃, 158 ℃, 160 ℃, 162 ℃, 165 ℃, 168 ℃, 170 ℃, 172 ℃, 175 ℃, 178 ℃ or 180 ℃ and the like; the screw rotation speed is 190-800r/min, for example, 190r/min, 200r/min, 250r/min, 300r/min, 350r/min, 400r/min, 450r/min, 500r/min, 550r/min, 600r/min, 650r/min, 700r/min, 750r/min or 800 r/min.
As a preferred technical scheme of the invention, the preparation method comprises the following steps:
(1) adding the filler into a high-speed mixing machine, heating to 110-120 ℃, stirring for 5-10min at the rotating speed of 1200-1480r/min, then adding a coupling agent, keeping the rotating speed, and mixing for 4-6min to obtain the modified filler;
(2) adding the rest components into the modified filler obtained in the step (1), keeping the rotating speed of 1200-1480r/min, and continuously mixing for 5-10 min;
(3) and (3) adding the mixed material obtained in the step (2) into a double-screw extruder, setting the head temperature at 150-.
In a third aspect, the present invention provides the use of the above-described filler masterbatch in a polypropylene wiredrawing stock.
In a fourth aspect, the present invention provides a polypropylene wiredrawing stock comprising polypropylene and the filling masterbatch provided in the first aspect of the present invention.
As a preferred technical scheme of the invention, the filling master batch accounts for 8-20% of the polypropylene wiredrawing material by mass; for example, it may be 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, or the like.
Preferably, the filling master batch accounts for 10-15% of the polypropylene wiredrawing material by mass.
The filling master batch provided by the invention is beneficial to improving the mechanical strength of the polypropylene wiredrawing material under a proper addition amount. When the addition amount is too small, the corresponding effect cannot be achieved; when the amount is too large, the strength of the polypropylene strand decreases.
Compared with the prior art, the invention has the following beneficial effects:
the invention adopts two polyethylene and polypropylene wax with different melt indexes to be matched to replace a low-melt-index polyethylene/polypropylene, paraffin wax and stearic acid system, so as to obtain the filling master batch with good high temperature resistance, wherein the fuming temperature of the filling master batch reaches 260 ℃, and the fuming problem in the polypropylene wire drawing production process is improved while the mechanical performance of the polypropylene wire drawing machine is improved.
Detailed Description
The technical solution of the present invention is further illustrated by the following specific examples. It should be understood by those skilled in the art that the examples are only for the understanding of the present invention and should not be construed as the specific limitations of the present invention.
Example 1
The embodiment provides a filling master batch, which comprises the following components in percentage by weight:
wherein, the grain diameter of the filler is 2-10 μm, the melt index of the low-melt index polyethylene is 0.01g/10min, and the melt index of the high-melt index polyethylene is 40g/10 min.
The preparation method of the filling master batch comprises the following steps:
(1) adding the filler into a high-speed mixer, heating to 110 ℃, stirring for 5min at the rotating speed of 1480r/min, then adding a coupling agent, keeping the rotating speed, and mixing for 4min to obtain a modified filler;
(2) adding the rest components into the modified filler obtained in the step (1), keeping the rotating speed of 1480r/min, and continuously mixing for 5 min;
(3) and (3) adding the mixed material obtained in the step (2) into a double-screw extruder, setting the temperature of a machine head to be 150 ℃, the temperature of an extrusion section to be 150 ℃ and the rotating speed of a screw to be 190r/min, and extruding to obtain the filling master batch.
Example 2
The embodiment provides a filling master batch, which comprises the following components in percentage by weight:
wherein, the grain diameter of the filler is 2-10 μm, the melt index of the low-melt index polyethylene is 2g/10min, and the melt index of the high-melt index polyethylene is 30g/10 min.
The preparation method of the filling master batch comprises the following steps:
(1) adding the filler into a high-speed mixer, heating to 120 ℃, stirring for 10min at the rotating speed of 1200r/min, then adding the coupling agent, keeping the rotating speed, and mixing for 6min to obtain the modified filler;
(2) adding the rest components into the modified filler obtained in the step (1), keeping the rotating speed of 1200r/min, and continuously mixing for 10 min;
(3) and (3) adding the mixed material obtained in the step (2) into a double-screw extruder, setting the temperature of a machine head to be 180 ℃, the temperature of an extrusion section to be 180 ℃, and the rotating speed of a screw to be 800r/min, and extruding to obtain the filling master batch.
Example 3
The embodiment provides a filling master batch, which comprises the following components in percentage by weight:
wherein, the grain diameter of the filler is 2-10 μm, the melt index of the low-melt index polyethylene is 1.5g/10min, and the melt index of the high-melt index polyethylene is 20g/10 min.
The preparation method of the filling master batch comprises the following steps:
(1) adding the filler into a high-speed mixer, heating to 115 ℃, stirring for 8min at the rotating speed of 1300r/min, then adding the coupling agent, keeping the rotating speed, and mixing for 5min to obtain the modified filler;
(2) adding the rest components into the modified filler obtained in the step (1), keeping the rotating speed of 1300r/min, and continuously mixing for 8 min;
(3) and (3) adding the mixed material obtained in the step (2) into a double-screw extruder, setting the temperature of a machine head to be 170 ℃, the temperature of an extrusion section to be 170 ℃ and the rotating speed of a screw to be 500r/min, and extruding to obtain the filling master batch.
Example 4
The embodiment provides a filling master batch, which comprises the following components in percentage by weight:
wherein, the grain diameter of the filler is 10-20 μm, the melt index of the low-melt index polyethylene is 0.5g/10min, and the melt index of the high-melt index polyethylene is 40g/10 min.
The preparation method of the filling master batch comprises the following steps:
(1) adding the filler into a high-speed mixer, heating to 110 ℃, stirring for 6min at the rotating speed of 1400r/min, then adding the coupling agent, keeping the rotating speed, and mixing for 4.5min to obtain the modified filler;
(2) adding the rest components into the modified filler obtained in the step (1), keeping the rotating speed of 1400r/min, and continuously mixing for 6 min;
(3) and (3) adding the mixed material obtained in the step (2) into a double-screw extruder, setting the temperature of a machine head to be 160 ℃, the temperature of an extrusion section to be 160 ℃ and the rotating speed of a screw to be 300r/min, and extruding to obtain the filling master batch.
Example 5
The embodiment provides a filling master batch, which comprises the following components in percentage by weight:
wherein, the grain diameter of the filler is 10-20 μm, the melt index of the low-melt index polyethylene is 1g/10min, and the melt index of the high-melt index polyethylene is 40g/10 min.
The preparation method of the filling master batch comprises the following steps:
(1) adding the filler into a high-speed mixer, heating to 120 ℃, stirring for 8min at the rotating speed of 1400r/min, then adding the coupling agent, keeping the rotating speed, and mixing for 5.5min to obtain the modified filler;
(2) adding the rest components into the modified filler obtained in the step (1), keeping the rotating speed of 1400r/min, and continuously mixing for 8 min;
(3) and (3) adding the mixed material obtained in the step (2) into a double-screw extruder, setting the head temperature to be 165 ℃, the extrusion section temperature to be 165 ℃ and the screw rotating speed to be 400r/min, and extruding to obtain the filling master batch.
Comparative example 1
A filling material, which differs from example 5 in that it comprises the following components in weight percent:
the filled masterbatches provided in examples 1 to 5 and comparative example 1 above were placed in an oven and heated slowly to determine the fuming temperature. The results show that the fuming temperature of the filler concentrates provided in examples 1-5 is 260 ℃ and the fuming temperature of the filler concentrate provided in comparative example 1 is 180 ℃.
Application examples 1 to 6
The filling master batch provided in example 5 and polypropylene particles were mixed uniformly by a high mixing machine (the filling master batch accounts for 8%, 10%, 12%, 15%, 18% and 20% of the total mass of the filling master batch and the polypropylene particles, respectively), added into an extrusion flat film and flat filament machine, flat-film at 260 ℃, cooled, then drawn by a drawing hot-air box at 140 ℃, finally set in a setting hot-air box at 100 ℃ to form polypropylene drawn filaments.
Application of comparative examples 1 to 6
The filling master batch provided in the comparative example 1 and the polypropylene particles are uniformly mixed by a high mixing machine (the filling master batch accounts for 8 percent, 10 percent, 12 percent, 15 percent, 18 percent and 20 percent of the total mass of the filling master batch and the polypropylene particles respectively), added into an extrusion flat film and flat filament machine, subjected to flat film at 260 ℃, cooled, stretched by a drawing hot air box at 140 ℃, and finally shaped in a shaping hot air box at 100 ℃ to form the polypropylene drawn filament.
The mechanical properties of the polypropylene strands provided in the above application examples 1 to 6 and application comparative examples 1 to 6 were measured, and the results are shown in the following Table 1:
TABLE 1
Application examples | 1 | 2 | 3 | 4 | 5 | 6 |
Addition amount of filling master batch | 8% | 10% | 12% | 15% | 18% | 20% |
Tensile Strength (MPa) | 25 | 23 | 21 | 20 | 18 | 16 |
Elongation at Break (%) | 15 | 12 | 11 | 9 | 8 | 6 |
Comparative application | 1 | 2 | 3 | 4 | 5 | 6 |
Addition amount of filling master batch | 8% | 10% | 12% | 15% | 18% | 20% |
Tensile Strength (MPa) | 20 | 18 | 17 | 15 | 13 | 11 |
Elongation at Break (%) | 8 | 7 | 7 | 6 | 6 | 5 |
In conclusion, the filling master batch provided by the invention has good high-temperature resistance, and can improve the fuming problem in the polypropylene drawing production process; compared with the traditional filling master batch, the mechanical performance of the polypropylene drawn wire prepared from the filling master batch provided by the invention is improved.
The applicant declares that the above description is only a specific embodiment of the present invention, but the scope of the present invention is not limited thereto, and it should be understood by those skilled in the art that any changes or substitutions that can be easily conceived by those skilled in the art within the technical scope of the present invention are within the scope and disclosure of the present invention.
Claims (18)
1. The filling master batch is characterized by comprising the following components in percentage by weight:
the low-melt index polyethylene has a melt index of 0.01-1g/10min, and the high-melt index polyethylene has a melt index of 30-40g/10 min;
the filler is selected from one or a combination of at least two of calcium carbonate, kaolin, silicon dioxide or wollastonite;
the filling master batch further comprises 0.5 to 1 wt% of a lubricant;
the lubricant is ethylene bisstearamide and/or pentaerythritol tetrastearate.
2. The filled masterbatch according to claim 1, wherein the filler has a particle size of 2 to 20 μm.
3. The filled masterbatch according to claim 1, wherein the coupling agent is a titanate coupling agent and/or a silane coupling agent.
4. The filled masterbatch of claim 3, wherein the titanate coupling agent is selected from one or a combination of at least two of isopropyl tris (dioctylphosphoato) titanate, isopropyl dioleaato (dioctylphosphoato) titanate, triisostearoyl isopropyl titanate, isopropyl tris (dioctylphosphoato) titanate or isopropyl distearoylmethacryloyl titanate.
5. The filling masterbatch of claim 3, wherein the silane coupling agent is selected from one or a combination of at least two of gamma-aminopropyltriethoxysilane, gamma- (2, 3-glycidoxy) propyltrimethoxysilane, vinyltriethoxysilane, or gamma-methacrylate trimethoxysilane.
6. A process for preparing a filled masterbatch according to any one of claims 1 to 5, wherein the process comprises the steps of:
(1) mixing and reacting a filler and a coupling agent to obtain a modified filler;
(2) mixing the modified filler obtained in the step (1) with the rest of components;
(3) extruding the mixed material obtained in the step (2) through an extruder to obtain the filling master batch.
7. The method of manufacturing according to claim 6, further comprising: drying the filler prior to said mixing in step (1).
8. The method for preparing the compound of claim 7, wherein the drying method comprises the following steps: adding the filler into a high-speed mixer, heating to 110-120 ℃, and stirring for 5-10min at the rotating speed of 1200-1480 r/min.
9. The method according to claim 6, wherein the mixing in the steps (1) and (2) is performed in a high-speed mixer.
10. The method as claimed in claim 6, wherein the mixing in step (1) is carried out at a stirring rate of 1200-1480r/min for a period of 4-6 min.
11. The method as claimed in claim 6, wherein the mixing in step (2) is carried out at a stirring rate of 1200-1480r/min for a period of 5-10 min.
12. The production method according to claim 6, wherein the extruder in the step (3) is a twin-screw extruder.
13. The method as claimed in claim 12, wherein the head temperature of the twin-screw extruder is 150-180 ℃, the temperature of the extrusion section is 150-180 ℃, and the screw rotation speed is 190-800 r/min.
14. The method of claim 6, comprising the steps of:
(1) adding the filler into a high-speed mixing machine, heating to 110-120 ℃, stirring for 5-10min at the rotating speed of 1200-1480r/min, then adding a coupling agent, keeping the rotating speed, and mixing for 4-6min to obtain the modified filler;
(2) adding the rest components into the modified filler obtained in the step (1), keeping the rotating speed of 1200-1480r/min, and continuously mixing for 5-10 min;
(3) and (3) adding the mixed material obtained in the step (2) into a double-screw extruder, setting the head temperature at 150-.
15. Use of a filler masterbatch according to any one of claims 1 to 5 for polypropylene wiredrawing stock.
16. A polypropylene wiredrawing stock comprising polypropylene and the filled masterbatch of any one of claims 1-5.
17. The polypropylene wiredrawing stock according to claim 16, wherein the filler masterbatch is 8 to 20% by mass of the polypropylene wiredrawing stock.
18. The polypropylene wiredrawing stock according to claim 16, wherein the filler masterbatch is 10 to 15% by mass of the polypropylene wiredrawing stock.
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CN201810836982.6A CN109135008B (en) | 2018-07-26 | 2018-07-26 | Filling master batch, preparation method and application thereof, and polypropylene wiredrawing material containing filling master batch |
Applications Claiming Priority (1)
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EP0628592A1 (en) * | 1993-06-11 | 1994-12-14 | FELIX SCHOELLER JR. FOTO- UND SPEZIALPAPIERE GmbH & Co. KG. | Premixture, masterbatch or coating compound for the preparation of photographic layers |
CN103572392A (en) * | 2013-09-29 | 2014-02-12 | 桐城市福润包装材料有限公司 | Plastic weaving bag production process |
CN105400064A (en) * | 2015-11-11 | 2016-03-16 | 广东碧盛环球环保材料有限公司 | Filling masterbatch and preparation method thereof |
CN108047537A (en) * | 2017-12-26 | 2018-05-18 | 上海邦中高分子材料有限公司 | It is a kind of to be used to obstruct coupling anti-oxidative special color master batch of bottle and preparation method thereof |
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EP0628592A1 (en) * | 1993-06-11 | 1994-12-14 | FELIX SCHOELLER JR. FOTO- UND SPEZIALPAPIERE GmbH & Co. KG. | Premixture, masterbatch or coating compound for the preparation of photographic layers |
CN103572392A (en) * | 2013-09-29 | 2014-02-12 | 桐城市福润包装材料有限公司 | Plastic weaving bag production process |
CN105400064A (en) * | 2015-11-11 | 2016-03-16 | 广东碧盛环球环保材料有限公司 | Filling masterbatch and preparation method thereof |
CN108047537A (en) * | 2017-12-26 | 2018-05-18 | 上海邦中高分子材料有限公司 | It is a kind of to be used to obstruct coupling anti-oxidative special color master batch of bottle and preparation method thereof |
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Effective date of registration: 20221102 Address after: No.28 Guanghua North Road, Maoming, Guangdong 525000 Patentee after: Guangdong Zhonghe Plastic Co.,Ltd. Address before: 525099 Room 203, Floor 2, Yongsheng Building, No. 28, Guanghua North Road, Maonan District, Maoming City, Guangdong Province Patentee before: GUANGDONG ZHONGHE ZHONGDE FINE CHEMICAL RESEARCH DEVELOPMENT Co.,Ltd. |