CN111978632A - Polypropylene fiber anti-aging agent master batch, preparation method thereof and polypropylene fiber - Google Patents
Polypropylene fiber anti-aging agent master batch, preparation method thereof and polypropylene fiber Download PDFInfo
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- CN111978632A CN111978632A CN202010771884.6A CN202010771884A CN111978632A CN 111978632 A CN111978632 A CN 111978632A CN 202010771884 A CN202010771884 A CN 202010771884A CN 111978632 A CN111978632 A CN 111978632A
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- 239000004743 Polypropylene Substances 0.000 title claims abstract description 138
- -1 Polypropylene Polymers 0.000 title claims abstract description 137
- 229920001155 polypropylene Polymers 0.000 title claims abstract description 136
- 239000000835 fiber Substances 0.000 title claims abstract description 103
- 239000004594 Masterbatch (MB) Substances 0.000 title claims abstract description 59
- 230000003712 anti-aging effect Effects 0.000 title claims abstract description 53
- 239000003795 chemical substances by application Substances 0.000 title claims abstract description 40
- 238000002360 preparation method Methods 0.000 title abstract description 10
- 239000002250 absorbent Substances 0.000 claims abstract description 38
- 230000002745 absorbent Effects 0.000 claims abstract description 38
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 35
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 32
- 239000002105 nanoparticle Substances 0.000 claims abstract description 23
- 229920000092 linear low density polyethylene Polymers 0.000 claims abstract description 20
- 239000004707 linear low-density polyethylene Substances 0.000 claims abstract description 20
- 239000006097 ultraviolet radiation absorber Substances 0.000 claims description 21
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 claims description 14
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 claims description 14
- 238000001816 cooling Methods 0.000 claims description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 8
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- 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
- 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
- D01F1/106—Radiation shielding agents, e.g. absorbing, reflecting agents
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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
- 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
- C08J2423/08—Copolymers of ethene
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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
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
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Abstract
The invention discloses a polypropylene fiber anti-aging agent master batch, a preparation method thereof and polypropylene fibers, wherein the polypropylene fiber anti-aging agent master batch comprises 20-40 wt% of polypropylene, 4-56 wt% of LLDPE, 20-40 wt% of POE, 3-9 wt% of antioxidant and 1-7 wt% of ultraviolet absorbent. According to the polypropylene fiber anti-aging agent master batch, the preparation method thereof and the polypropylene fiber, the LLDPE, the POE or the inorganic nanoparticles are added into the polypropylene matrix, and the antioxidant and the ultraviolet absorbent are added, so that the toughness of the polypropylene fiber can be obviously improved, the anti-aging performance of the polypropylene fiber can be improved, and the service life of the polypropylene fiber is prolonged.
Description
Technical Field
The invention relates to the technical field of fiber materials, in particular to the technical field of polypropylene fibers, and particularly relates to an anti-aging master batch for polypropylene fibers, a preparation method of the anti-aging master batch and polypropylene fibers.
Background
The polypropylene fiber has the characteristics of low density, high strength, excellent chemical resistance and the like, and has a wide market prospect in the fields of geotechnical materials, carpets, lawns and the like at present.
However, the polypropylene fiber has the disadvantages of poor toughness, low aging resistance and the like, and the service life of the polypropylene fiber is reduced. Because toughness and ageing resistance have a certain opposite relation, the existing ageing resistance agent can only improve the ageing resistance of the polypropylene fiber, and can also influence the toughness of the polypropylene fiber, so that the toughness of the polypropylene fiber is poor. The problem of how to consider the aging resistance of the polypropylene fiber when improving the toughness of the polypropylene fiber is not solved effectively at present.
Disclosure of Invention
In view of the above-mentioned defects or shortcomings in the prior art, it is desirable to provide an age resister masterbatch for polypropylene fibers, a preparation method thereof, and polypropylene fibers.
In a first aspect, the invention provides an age resister master batch for polypropylene fibers, which comprises 20-40% by weight of polypropylene, 4-56% by weight of LLDPE, 20-40% by weight of POE, 3-9% by weight of antioxidant and 1-7% by weight of ultraviolet absorber.
Further, the antioxidant comprises antioxidant 1010 and antioxidant 168, and the weight ratio of the antioxidant 1010 to the antioxidant 168 is 1: 2.
Further, the ultraviolet absorbent comprises an ultraviolet absorbent UV326 and an ultraviolet absorbent UV531, and the weight ratio of the ultraviolet absorbent UV326 to the ultraviolet absorbent UV531 is 1: 1.
Further, the weight percentage of the polypropylene is 30%, the weight percentage of the LLDPE is 30%, the weight percentage of the POE is 30%, the weight percentage of the antioxidant is 6%, and the weight percentage of the ultraviolet absorbent is 4%.
In a second aspect, the application also provides an age resister master batch for polypropylene fibers, which comprises 86-89% by weight of polypropylene, 1-4% by weight of inorganic nanoparticles, 3-9% by weight of an antioxidant and 1-7% by weight of an ultraviolet absorber.
Further, the antioxidant comprises antioxidant 1010 and antioxidant 168, and the weight ratio of the antioxidant 1010 to the antioxidant 168 is 1: 2.
Further, the ultraviolet absorbent comprises an ultraviolet absorbent UV326 and an ultraviolet absorbent UV531, and the weight ratio of the ultraviolet absorbent UV326 to the ultraviolet absorbent UV531 is 1: 1.
Further, the inorganic nanoparticles are silica nanoparticles.
In a third aspect, the application also provides a polypropylene fiber, which includes the above polypropylene fiber anti-aging agent masterbatch.
In a third aspect, the application further provides a preparation method of the polypropylene fiber anti-aging agent masterbatch, including:
uniformly mixing polypropylene, LLDPE, POE, antioxidant and ultraviolet absorbent or polypropylene, inorganic nano particles, antioxidant and ultraviolet absorbent to obtain a blend;
and sequentially carrying out melting treatment, wire extrusion treatment, cooling treatment, drying treatment and grain cutting treatment on the blend to obtain the polypropylene fiber anti-aging agent master batch.
According to the polypropylene fiber anti-aging agent master batch, the preparation method thereof and the polypropylene fiber, the LLDPE, the POE or the inorganic nanoparticles are added into the polypropylene matrix, and the antioxidant and the ultraviolet absorbent are added, so that the toughness of the polypropylene fiber can be obviously improved, the anti-aging performance of the polypropylene fiber can be improved, and the service life of the polypropylene fiber is prolonged.
Drawings
Other features, objects and advantages of the invention will become more apparent upon reading of the detailed description of non-limiting embodiments made with reference to the following drawings:
FIG. 1 is a flow chart of polypropylene fiber antiaging agent masterbatch provided by the embodiment of the invention;
FIG. 2 is an infrared spectrum provided by an embodiment of the present invention.
Detailed Description
The present invention will be described in further detail with reference to the accompanying drawings and examples. It is to be understood that the specific embodiments described herein are merely illustrative of the relevant invention and not restrictive of the invention. It should be noted that, for convenience of description, only the portions related to the present invention are shown in the drawings.
It should be noted that the embodiments and features of the embodiments may be combined with each other without conflict. The present invention will be described in detail below with reference to the embodiments with reference to the attached drawings.
The invention provides an age resister master batch for polypropylene fibers, which comprises 20-40 wt% of polypropylene, 4-56 wt% of LLDPE, 20-40 wt% of POE, 3-9 wt% of antioxidant and 1-7 wt% of ultraviolet absorbent.
In this embodiment, the polypropylene fiber age resister masterbatch is toughened and modified by adding LLDPE (linear low density polyethylene) and POE (ethylene-1-octene copolymer) into the polypropylene matrix, so that the toughness of the polypropylene fiber prepared by using the polypropylene fiber age resister masterbatch can be obviously improved. The mechanism of improving the toughness of the polypropylene fiber by LLDPE and POE is as follows: the two components can inhibit the crystallization of polypropylene through a synergistic effect, form microcrystals and further improve the toughness of the polypropylene fiber.
Meanwhile, the antioxidant and the ultraviolet absorber are added into the polypropylene matrix, so that the oxidation resistance and the ultraviolet radiation resistance of the polypropylene fiber prepared by using the polypropylene fiber anti-aging agent master batch can be obviously improved, and the aging resistance of the polypropylene fiber is further improved. Therefore, the polypropylene fiber anti-aging agent masterbatch provided by the embodiment can improve the toughness of the polypropylene fiber and simultaneously improve the anti-aging performance of the polypropylene fiber, so that the balance between the oxidation resistance and the toughness is good, and the service life of the polypropylene fiber is prolonged.
In addition, the compatibility among polyethylene, LLDPE and POE is good, and a compatilizer is not needed, so that the preparation cost of the polypropylene fiber is reduced.
The polypropylene fiber anti-aging agent adopts a master batch structure, so that the polypropylene fiber anti-aging agent can be uniformly dispersed in a polypropylene raw material when polypropylene is prepared, and the anti-aging property and the toughness of polypropylene fibers are further improved.
In some preferred embodiments, the polypropylene is 30 wt%, the LLDPE is 30 wt%, the POE is 30 wt%, the antioxidant is 6 wt%, and the uv absorber is 4 wt%. When the weight of each component is proportioned in this way, the anti-aging performance and toughness of the polypropylene fiber anti-aging agent master batch to the polypropylene fiber can be improved to the maximum.
In some preferred embodiments, the antioxidants include antioxidant 1010 and antioxidant 168, and the weight ratio of antioxidant 1010 to antioxidant 168 is 1: 2.
In this embodiment, the antioxidant is prepared by compounding two kinds of oxidants, and the weight ratio of the antioxidant 1010 to the antioxidant 168 is 1:2, so that the polypropylene fiber prepared from the polypropylene fiber anti-aging agent masterbatch has the best antioxidant performance.
In some preferred embodiments, the ultraviolet absorber includes an ultraviolet absorber UV326 and an ultraviolet absorber UV531, and the weight ratio of the ultraviolet absorber UV326 to the ultraviolet absorber UV531 is 1: 1.
In this embodiment, the ultraviolet absorbent is prepared by compounding two oxidants, and the weight ratio of the ultraviolet absorbent UV326 to the ultraviolet absorbent UV531 is 1:1, so that the polypropylene fiber prepared from the polypropylene fiber anti-aging agent masterbatch has the best ultraviolet radiation resistance.
The application also provides polypropylene fiber anti-aging agent master batch which comprises 86-89% by weight of polypropylene, 1-4% by weight of inorganic nano particles, 3-9% by weight of antioxidant and 1-7% by weight of ultraviolet absorbent.
In this example, the specific surface area of the inorganic nanoparticles is large and the contact area with the polypropylene matrix is large by adding the inorganic nanoparticles to the polypropylene matrix. The inorganic nano particles can initiate and deflect microcracks generated in the matrix, and absorb the impact energy of the outside to the matrix, so that the toughness of the medical polypropylene fiber is improved. Specifically, the method comprises the following steps: when the medical polypropylene fiber is impacted by external force, microcracks can be generated, and when the microcracks meet the inorganic nano particles, the microcracks can deflect and initiate new cracks to absorb more impact force, so that the toughening performance of the polypropylene fiber is improved. Meanwhile, the antioxidant and the ultraviolet absorber are added into the polypropylene matrix, so that the oxidation resistance and the ultraviolet radiation resistance of the polypropylene fiber prepared by using the polypropylene fiber anti-aging agent master batch can be obviously improved, and the aging resistance of the polypropylene fiber is further improved. Therefore, the polypropylene fiber anti-aging agent masterbatch provided by the embodiment can improve the toughness of the polypropylene fiber and simultaneously improve the anti-aging performance of the polypropylene fiber, so that the balance between the oxidation resistance and the toughness is good, and the service life of the polypropylene fiber is prolonged.
In some preferred embodiments, the antioxidants include antioxidant 1010 and antioxidant 168, and the weight ratio of antioxidant 1010 to antioxidant 168 is 1: 2. The ultraviolet absorbent comprises an ultraviolet absorbent UV326 and an ultraviolet absorbent UV531, and the weight ratio of the ultraviolet absorbent UV326 to the ultraviolet absorbent UV531 is 1: 1. The beneficial effects of such an arrangement of antioxidants and UV absorbers are not described herein in detail, see above.
In some preferred embodiments, the inorganic nanoparticles are silica nanoparticles.
In the embodiment, the cost of the silica nanoparticles is relatively low, so that the cost of the polypropylene fiber anti-aging agent master batch is relatively low. Of course, in other embodiments, the inorganic nanoparticles may also be titanium dioxide nanoparticles or graphene nanoparticles, etc. Wherein the particle size of the inorganic nano particles is 50-120 nm.
The application also provides a polypropylene fiber, which comprises the polypropylene fiber anti-aging agent master batch. Because the polypropylene fiber anti-aging agent master batch in the embodiment is used in the polypropylene fiber, the polypropylene fiber has better toughness and better anti-aging performance.
The application also provides a preparation method of the polypropylene fiber anti-aging agent master batch, which comprises the following steps:
s100: uniformly mixing polypropylene, LLDPE, POE, antioxidant and ultraviolet absorbent or polypropylene, inorganic nano particles, antioxidant and ultraviolet absorbent to obtain a blend;
s200: and sequentially carrying out melting treatment, wire extrusion treatment, cooling treatment, drying treatment and grain cutting treatment on the blend to obtain the polypropylene fiber anti-aging agent master batch.
In this embodiment, the components of the polypropylene fiber age resister masterbatch are mixed together to obtain a blend, and then the blend is subjected to melting treatment, extruding treatment, cooling treatment, drying treatment and dicing treatment in sequence to obtain the polypropylene fiber age resister masterbatch. Wherein, carry out melting and crowded silk processing through the twin-screw extruder, the temperature in twin-screw one to ten district is respectively: 120 deg.C, 140 deg.C, 160 deg.C, 180 deg.C, 190 deg.C, 200 deg.C, 190 deg.C, 180 deg.C, and a stable pressure of 1-2 MPa. The cooling treatment can be air cooling or liquid cooling, wherein liquid cooling is preferred, and the cooling effect is good. The drying treatment adopts a hot air drying process.
To further illustrate the performance of the polypropylene fiber age resistor masterbatch provided herein, polypropylene fibers are provided hereinThe performance of the age resister master batch is subjected to accelerated aging test, and the accelerated aging test comprises the following contents: placing the sample in BASN-100 accelerated aging test box at 70 deg.C and blackboard temperature of 63 + -3 deg.C, and light intensity of 60W/M2The test time is 144 h.
The application provides 1 group of reference examples (group numbers are respectively A) and 3 groups of test examples (group numbers are respectively B, C and D), wherein the test objects in the 3 groups of test examples are the polypropylene fiber anti-aging agent master batch of the application, and the components of the polypropylene fiber anti-aging agent master batch in the B group are as follows: 30% of polypropylene, 30% of LLDPE, 30% of POE, 3% of antioxidant and 7% of ultraviolet absorbent; the polypropylene fiber anti-aging agent master batch in the group C comprises the following components: 30% of polypropylene, 30% of LLDPE, 30% of POE, 6% of antioxidant and 4% of ultraviolet absorbent; the polypropylene fiber anti-aging agent master batch in the group D comprises the following components: 30 percent of polypropylene, 30 percent of LLDPE, 30 percent of POE, 9 percent of antioxidant and 1 percent of ultraviolet absorbent. The antioxidant is composed of antioxidant 1010 and antioxidant 168 in a weight ratio of 1:2, and the ultraviolet absorbent is composed of ultraviolet absorbent UV326 and ultraviolet absorbent UV531 in a weight ratio of 1: 1. The test object in the 1 group of control examples was only polypropylene master batch. The settings were completely identical in the 4 sets of experiments except for the test subjects.
In the aspect of melt index measurement, the melt index measurement is tested according to GB/T3682-2000, wherein the test temperature is set to be 230 ℃, the load is 5kg, the sampling interval time is 30s, 5 sample strips are cut out repeatedly in each group, after the sample strips are cooled, the sample strips are weighed by a precision electronic balance, and the average value is taken. The melt indices before and after aging in the 4 components are shown in the following table:
group number | Before aging (g/10min) | After aging (g/10min) | Amplification (g/10min) |
A | 3.2 | 41.2 | 38 |
B | 7.2 | 30.7 | 23.5 |
C | 6.8 | 28.1 | 21.3 |
D | 7.1 | 31.7 | 24.6 |
Based on the above table, it can be known that, compared with the pure polypropylene master batch, the polypropylene fiber anti-aging agent master batch has the advantages that the melt index increase amplitude of the polypropylene fiber anti-aging agent master batch after accelerated aging is reduced by about 40% on average, the anti-aging performance is obviously improved, wherein the melt index increase amplitude of the polypropylene fiber anti-aging agent master batch in the group C is the best, and the anti-aging performance is the best.
In the measurement of yellowness index, the measurement of yellowness index is carried out according to the international standard method GB/T2409-1980, and the measurement result shows that the material has yellow color if the value is positive and blue color if the value is negative, wherein the value is based on magnesium oxide and the light source of the international commission on illumination (CIE) standard C. The method is adopted to test each group of samples which are not aged by the accelerated ageing oven, master batches of each group are made into film samples according to the specification of 60mm multiplied by 1mm, and the test results are shown in the following table:
group number | Before irradiation | After irradiation |
A | -48 | 20 |
B | -35 | 5 |
C | -34 | -25 |
D | -36 | 3 |
As can be seen from the above table, the yellowness index of the polypropylene fiber anti-aging agent master batch added with the antioxidant is larger than that of the pure polypropylene master batch and basically the same, and for the irradiated sample, the yellowness index of the group C is the smallest, and the compounding effect of the antioxidant and the ultraviolet absorbent is the best.
And (3) carrying out infrared spectrometry on the polypropylene master batch subjected to the aging treatment, wherein a Fourier infrared spectrometer is adopted for carrying out the spectrometry, and the test parameters are as follows: the scanning was repeated 8 times in the wavenumber range of 4500--1Resolution 4.0cm-1. The infrared spectrum is shown in figure 2.
As can be seen from FIG. 2, the peak area of carbonyl degradation in group C is the smallest, the degree of degradation is the smallest, and the anti-thermal oxidative aging modification performance is the best.
In the aspect of X-ray diffraction measurement, each group of master batches are prepared into a powdery sample, XRD test is carried out, a Cu target Ka ray is selected by an X-ray diffractometer, the voltage is 40KV, the current is 40mA, the scanning speed is 5 degrees/min, and the scanning range is 5 degrees to 30 degrees. The crystallinity and grain size of each group of master batches after accelerated aging are shown in the following table:
group number | Degree of crystallization/%) | Crystal size/A |
A | 27.8 | -215 |
B | 31.5 | -179 |
C | 33.5 | -156 |
D | 30.2 | -192 |
As can be seen from the above table, the crystallinity in group C is 33.5% at the maximum, and the grain size is-156 nm at the minimum, which indicates that LLDPE and POE act synergistically to toughen PP, inhibit the crystallization of PP, and make it form microcrystals, and the toughness is improved.
The foregoing description is only exemplary of the preferred embodiments of the invention and is illustrative of the principles of the technology employed. It will be appreciated by those skilled in the art that the scope of the invention herein disclosed is not limited to the particular combination of features described above, but also encompasses other arrangements formed by any combination of the above features or their equivalents without departing from the spirit of the invention. For example, the above features and (but not limited to) features having similar functions disclosed in the present invention are mutually replaced to form the technical solution.
Claims (10)
1. The polypropylene fiber anti-aging agent master batch is characterized by comprising 20-40 wt% of polypropylene, 4-56 wt% of LLDPE, 20-40 wt% of POE, 3-9 wt% of antioxidant and 1-7 wt% of ultraviolet absorbent.
2. The polypropylene fiber age resistor masterbatch of claim 1, wherein the antioxidant comprises antioxidant 1010 and antioxidant 168, and the weight ratio of the antioxidant 1010 to the antioxidant 168 is 1: 2.
3. The polypropylene fiber anti-aging master batch according to claim 1, wherein the ultraviolet absorber comprises an ultraviolet absorber UV326 and an ultraviolet absorber UV531, and the weight ratio of the ultraviolet absorber UV326 to the ultraviolet absorber UV531 is 1: 1.
4. The polypropylene fiber anti-aging agent masterbatch of claim 1, wherein the polypropylene is 30 wt%, the LLDPE is 30 wt%, the POE is 30 wt%, the antioxidant is 6 wt%, and the ultraviolet absorber is 4 wt%.
5. The polypropylene fiber anti-aging agent master batch is characterized by comprising 86-89 wt% of polypropylene, 1-4 wt% of inorganic nanoparticles, 3-9 wt% of antioxidant and 1-7 wt% of ultraviolet absorber.
6. The polypropylene fiber age resistor masterbatch of claim 5, wherein the antioxidant comprises antioxidant 1010 and antioxidant 168, and the weight ratio of the antioxidant 1010 to the antioxidant 168 is 1: 2.
7. The polypropylene fiber anti-aging master batch according to claim 5, wherein the ultraviolet absorber comprises an ultraviolet absorber UV326 and an ultraviolet absorber UV531, and the weight ratio of the ultraviolet absorber UV326 to the ultraviolet absorber UV531 is 1: 1.
8. The polypropylene fiber anti-aging masterbatch according to claim 5, wherein the inorganic nanoparticles are silica nanoparticles.
9. A polypropylene fiber comprising the polypropylene fiber anti-aging agent master batch according to any one of claims 1 to 4 or 5 to 8.
10. A method for preparing the polypropylene fiber anti-aging agent masterbatch according to any one of claims 1 to 4 or 5 to 8, comprising:
uniformly mixing the polypropylene, the LLDPE, the POE, the antioxidant and the ultraviolet absorbent or the polypropylene, the inorganic nano particles, the antioxidant and the ultraviolet absorbent to obtain a blend;
and sequentially carrying out melting treatment, wire extrusion treatment, cooling treatment, drying treatment and grain cutting treatment on the blend to obtain the polypropylene fiber anti-aging agent master batch.
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112725963A (en) * | 2020-12-22 | 2021-04-30 | 南通新帝克单丝科技股份有限公司 | Large-diameter elastic monofilament and production method thereof |
CN114407443A (en) * | 2021-12-21 | 2022-04-29 | 日丰企业集团有限公司 | Oxygen-blocking and anti-scaling PP-RCT pipe and preparation method thereof |
Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1246549A (en) * | 1998-08-31 | 2000-03-08 | 中国科学院化学研究所 | Low-temp spinning technique for polypropylene fibre |
CN101870784A (en) * | 2010-03-29 | 2010-10-27 | 金发科技股份有限公司 | Impact resisting weather-proof polypropylene and preparation method thereof |
CN102002184A (en) * | 2010-10-08 | 2011-04-06 | 华南理工大学 | Enhanced toughened halogen-free flame-retardant polypropylene mixture and preparation method thereof |
CN102604209A (en) * | 2012-02-20 | 2012-07-25 | 金发科技股份有限公司 | Thermal-oxidizing-aging resisting polypropylene composite |
CN105237886A (en) * | 2015-10-30 | 2016-01-13 | 永高股份有限公司 | Preparation method for polypropylene-toughened impact-resistant tubular product |
CN106046550A (en) * | 2016-06-28 | 2016-10-26 | 邵炯 | High-temperature-resistant, aging-resistant and impact-resistant heat-conduction polypropylene material and preparing method thereof |
CN106280002A (en) * | 2016-08-31 | 2017-01-04 | 金田集团(桐城)塑业有限公司 | A kind of uvioresistant polypropylene film material |
CN106380687A (en) * | 2016-08-31 | 2017-02-08 | 金田集团(桐城)塑业有限公司 | Low-temperature-resistant polypropylene film material |
CN106589537A (en) * | 2016-12-06 | 2017-04-26 | 淄博龙沙高分子材料科技有限公司 | Master batch having light conversion function for preparing tomato greenhouse film |
CN107629314A (en) * | 2017-09-01 | 2018-01-26 | 金发科技股份有限公司 | A kind of polypropene composition and preparation method thereof |
CN108250579A (en) * | 2018-01-30 | 2018-07-06 | 浙江马新材料有限公司 | A kind of high-glossiness flame-retardant polypropylene composite and preparation method thereof |
CN109054170A (en) * | 2018-06-27 | 2018-12-21 | 南通新帝克单丝科技股份有限公司 | A kind of anti-aging modified master batch of fibre-forming polymer and preparation method thereof |
-
2020
- 2020-08-04 CN CN202010771884.6A patent/CN111978632A/en active Pending
Patent Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1246549A (en) * | 1998-08-31 | 2000-03-08 | 中国科学院化学研究所 | Low-temp spinning technique for polypropylene fibre |
CN101870784A (en) * | 2010-03-29 | 2010-10-27 | 金发科技股份有限公司 | Impact resisting weather-proof polypropylene and preparation method thereof |
CN102002184A (en) * | 2010-10-08 | 2011-04-06 | 华南理工大学 | Enhanced toughened halogen-free flame-retardant polypropylene mixture and preparation method thereof |
CN102604209A (en) * | 2012-02-20 | 2012-07-25 | 金发科技股份有限公司 | Thermal-oxidizing-aging resisting polypropylene composite |
CN105237886A (en) * | 2015-10-30 | 2016-01-13 | 永高股份有限公司 | Preparation method for polypropylene-toughened impact-resistant tubular product |
CN106046550A (en) * | 2016-06-28 | 2016-10-26 | 邵炯 | High-temperature-resistant, aging-resistant and impact-resistant heat-conduction polypropylene material and preparing method thereof |
CN106280002A (en) * | 2016-08-31 | 2017-01-04 | 金田集团(桐城)塑业有限公司 | A kind of uvioresistant polypropylene film material |
CN106380687A (en) * | 2016-08-31 | 2017-02-08 | 金田集团(桐城)塑业有限公司 | Low-temperature-resistant polypropylene film material |
CN106589537A (en) * | 2016-12-06 | 2017-04-26 | 淄博龙沙高分子材料科技有限公司 | Master batch having light conversion function for preparing tomato greenhouse film |
CN107629314A (en) * | 2017-09-01 | 2018-01-26 | 金发科技股份有限公司 | A kind of polypropene composition and preparation method thereof |
CN108250579A (en) * | 2018-01-30 | 2018-07-06 | 浙江马新材料有限公司 | A kind of high-glossiness flame-retardant polypropylene composite and preparation method thereof |
CN109054170A (en) * | 2018-06-27 | 2018-12-21 | 南通新帝克单丝科技股份有限公司 | A kind of anti-aging modified master batch of fibre-forming polymer and preparation method thereof |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112725963A (en) * | 2020-12-22 | 2021-04-30 | 南通新帝克单丝科技股份有限公司 | Large-diameter elastic monofilament and production method thereof |
CN114407443A (en) * | 2021-12-21 | 2022-04-29 | 日丰企业集团有限公司 | Oxygen-blocking and anti-scaling PP-RCT pipe and preparation method thereof |
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