CN103289187B - Polypropylene composite, its preparation method and application thereof - Google Patents
Polypropylene composite, its preparation method and application thereof Download PDFInfo
- Publication number
- CN103289187B CN103289187B CN201310059538.5A CN201310059538A CN103289187B CN 103289187 B CN103289187 B CN 103289187B CN 201310059538 A CN201310059538 A CN 201310059538A CN 103289187 B CN103289187 B CN 103289187B
- Authority
- CN
- China
- Prior art keywords
- polypropylene composite
- polypropylene
- laser
- weighting agent
- composite
- 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.)
- Active
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Abstract
The present invention discloses a kind of polypropylene composite, its preparation method and application thereof.Polypropylene composite comprises the component of following weight part: polypropylene 30-100 part; Promotor 0.2-0.6 part; Laser absorbent 5-30 part; Compatilizer 0-8 part; Weighting agent 0-40 part; Tinting pigment 0-0.8 part; Oxidation inhibitor 0.1-1 part; Processing aid 0.1-1 part; Wherein, organophosphate compounds is adopted as promotion polypropylene composite to the promotor of laser absorption.The present invention also provides preparation method and the application thereof of above-mentioned polypropylene composite.The easy laser-marking of polypropylene composite of the present invention and effective, and good mechanical property.
Description
Technical field
The present invention relates to a kind of polypropylene composite, particularly relate to the application of a kind of polypropylene composite of laser-markable, its preparation method and this mixture.
Background technology
Laser-marking technology is compared with other printing technology, there is plurality of advantages, as mark not easily wipe, fast, can high, the environmental friendliness of time variable control, degree of freedom, it is made to apply widely, and carry out laser-marking also fast development thereupon at polymer surfaces, but the reason due to polypropylene self structure causes polypropylene to be not so good as the easy absorbing laser of the polymkeric substance such as ABS, PS, greatly limit polyacrylic application.Commonly use in prior art and add inorganic metal salt, metal oxide, inorganic phosphate in the polymer to the performance making polymkeric substance have laser labelling.Along with development and the polyacrylic extensive application of laser-marking technology, the research of the acrylic resin of commute laser-marking more and more becomes an emphasis.
Summary of the invention
In sum, the present invention is necessary the polypropylene composite providing a kind of easy laser-marking.
In addition, there is a need to the preparation method that a kind of above-mentioned polypropylene composite is provided.
In addition, there is a need to the application that a kind of above-mentioned polypropylene composite is provided.
A kind of polypropylene composite, comprises the component of following weight part:
Polypropylene 30-100 part;
Promotor 0.2-0.6 part;
Laser absorbent 5-30 part;
Compatilizer 0-8 part;
Weighting agent 0-40 part;
Tinting pigment 0-0.8 part;
Oxidation inhibitor 0.1-1 part;
Processing aid 0.1-1 part;
Wherein, described promotor is organophosphate compounds.
A kind of polypropylene composite, is made up of the component of following weight part:
Polypropylene 30-100 part;
Promotor 0.2-0.6 part;
Laser absorbent 5-30 part;
Compatilizer 0-8 part;
Weighting agent 0-40 part;
Tinting pigment 0-0.8 part;
Oxidation inhibitor 0.1-1 part;
Processing aid 0.1-1 part;
Wherein, described promotor is organophosphate compounds.
Wherein, polypropylene composite of the present invention does not comprise metal oxide, as antimonous oxide, antimony peroxide, zinc borate etc.
Wherein, the preferred 60-92 weight part of described polypropylene.
Wherein, the preferred 5-17 weight part of described laser absorbent, further preferred 8-17 weight part.
Wherein, the preferred 10-31 weight part of described weighting agent.
Wherein, described laser absorbent can for the material promoting polypropylene to become charcoal, at least one in preferred decabromodiphenyl oxide, TDE, brominated polystyrene, brominated epoxy resin or brominated triazine.
Wherein, at least one in described laser absorbent further preferably decabromodiphenyl oxide, TDE or brominated polystyrene.
Wherein, the promotor of organophosphate compounds of the present invention can improve the regular arrangement of polyacrylic molecular chain, promotes that polypropylene is to the absorption of laser.
Wherein, described promotor can be two (to tertiary butyl phenoxy group) sodium phosphate salt, 2,2'-methylene-biss (4,6-di-t-butyl) phenol sodium phosphate salts or 2, at least one in 2'-methylene-bis (4,6-di-tert-butyl-phenyl) phosphalugel.
Wherein, described polypropylene can be the combination of homo-polypropylene, block copolymerization polypropylene, atactic copolymerized polypropene or wherein at least two kinds of materials.
Wherein, described compatilizer can be 3-8 weight part.
Wherein, described compatilizer can be the graftomer of polypropylene and unsaturated carboxylic acid or the graftomer of polypropylene and unsaturated carboxylic acid acid anhydrides.
Wherein, described unsaturated carboxylic acid can be maleic acid.
Wherein, described unsaturated carboxylic acid acid anhydrides can be MALEIC ANHYDRIDE.
Wherein, described weighting agent can be at least one in talcum powder, calcium carbonate, barium sulfate, calcium sulfate, wollastonite, mica, glass microballon, glass fibre.
Wherein, described weighting agent can be the weighting agent through silane coupling agent or titanate coupling agent activation treatment.
Wherein, described tinting pigment can be 0.2-0.8 weight part.
Wherein, described tinting pigment is carbon black.Preferred thermally oxidized black further.
Wherein, described oxidation inhibitor is the mixture of any one and Hinered phenols primary antioxidant in phosphorous acid esters or thioether class auxiliary anti-oxidant.
Wherein, described processing aid is at least one in metal soap, stearic acid complex ester class, amides.
A preparation method for polypropylene composite, comprises the following steps:
In proportion the component except described weighting agent is placed in mixing machine mix and blend and obtains mixture, added by the main charging opening of gained mixture from twin screw extruder, the weighting agent of described ratio adds from the side loading mouth of twin screw extruder, extrudes, granulation, obtained polypropylene composite.
Wherein, the preparation method of above-mentioned polypropylene composite comprises the following steps:
In proportion the component except described weighting agent is placed in mixing machine mix and blend and obtains mixture in 5 minutes, the main charging opening of gained mixture from twin screw extruder is added, the weighting agent of described ratio adds from the side loading mouth of twin screw extruder, extrude, granulation, obtained polypropylene composite.
An application for above-mentioned polypropylene composite, described polypropylene composite is applied to automobile, household electrical appliances and field of electronics.
Compare prior art, polypropylene composite of the present invention adds promotor and the laser absorbent of the penetration enhancement laser of organic phosphate, make the easy laser-marking of polypropylene and effective, and, the good mechanical property of polypropylene composite of the present invention.
Embodiment
Below in conjunction with some embodiments, polypropylene composite of the present invention, preparation method and application thereof are described further.Specific embodiment is for further describing the present invention, non-limiting protection scope of the present invention.
Polypropylene composite of the present invention carries out following performance test according to standard system for batten:
Tensile strength is tested: according to ISO527 standard testing.
Modulus in flexure is tested: according to ISO178 standard testing.
Izod notched impact strength is tested: according to ISO180 standard testing, the breach type of sample is category-A breach.
Laser-marking performance test and evaluation method: on-gauge plate polypropylene composite being injection molded into 100mm × 100mm × 2mm, Nd:YAG laser apparatus (manufacture of great Cu laser Science and Technology Co., Ltd.) is adopted to test on-gauge plate, test wavelength is 1064nm test technology: electric current 15A, frequency 2.0KHz, step-length 0.003mm, adopt the method for range estimation to characterize marking effect, be divided into third-class, respectively as well, better and poor, wherein, good represent identify clear; Better expression mark is substantially clear; Difference represents that mark is fuzzy.
In all embodiments provided by the invention, the starting material provided all can obtain from market buying.Wherein,
Polypropylene-1 is selected from Maoming Petrochemical, trade mark EPC30R-H.
Polypropylene-2 is that CNOOC and Shell Petrochemicals Co., Ltd HP500N mixes by weight 1:1 ratio with Lanzhou Petrochemical SP179.
Two (to tertiary butyl phenoxy group) sodium phosphate salt, commercially available.
2,2'-methylene-bis (4,6-di-t-butyl) phenol sodium phosphate salt, commercially available.
2,2'-methylene-bis (4,6-di-tert-butyl-phenyl) phosphalugel, commercially available.
Decabromodiphenyl oxide is selected from Chemtura, trade mark DE-83R.
Brominated epoxy resin is selected from Korea S's space and enters, trade mark CXB-2000H.
Brominated triazine is selected from Korea S's space and enters, trade mark FR-245.
TDE is selected from Shouguang WeiDong Chemical Co., Ltd., trade mark RDT-3K.
Brominated polystyrene is selected from Chemtura, trade mark PBS-64HW.
Compatilizer-1 is selected from Chemtura, trade mark Polybond3200.
It is bright that compatilizer-2 is selected from Puli, trade mark Bondyram1001CN.
Carbon black is selected from Cabot M717.
Oxidation inhibitor selects Ciba Irganox1010 to mix by weight 1:1 ratio with Ciba Irgafos168 (Ciba).
Processing aid selects ethylene bis stearamide EBS, commercially available.
Embodiment 1-10
Get the component of listed weight part in table 1, component except weighting agent is placed in mixing machine mix and blend and obtains mixture in 5 minutes, the main charging opening of gained mixture from twin screw extruder is added, weighting agent adds from the side loading mouth of twin screw extruder, extrude, granulation, obtained polypropylene composite.
Gained polypropylene composite is tested its tensile strength, modulus in flexure, Izod notched impact strength and laser-marking performance also by the results are shown in Table 1 according to testing method.
Comparative example 1-10
Get the component of listed weight part in table 2, component except weighting agent is placed in mixing machine mix and blend and obtains mixture in 5 minutes, the main charging opening of gained mixture from twin screw extruder is added, weighting agent adds from the side loading mouth of twin screw extruder, extrude, granulation, obtained polypropylene composite.
Gained polypropylene composite is tested its tensile strength, modulus in flexure, Izod notched impact strength and laser-marking performance also by the results are shown in Table 2 according to testing method.
Embodiment 11-15, comparative example 11-14
Get the component of listed weight part in table 3, component except weighting agent is placed in mixing machine mix and blend and obtains mixture in 5 minutes, the main charging opening of gained mixture from twin screw extruder is added, weighting agent adds from the side loading mouth of twin screw extruder, extrude, granulation, obtained polypropylene composite.
Gained polypropylene composite is tested its tensile strength, modulus in flexure, Izod notched impact strength and laser-marking performance also by the results are shown in Table 3 according to testing method.
Embodiment 16-18, comparative example 15-18
Get the component of listed weight part in table 4, component except weighting agent is placed in mixing machine mix and blend and obtains mixture in 5 minutes, the main charging opening of gained mixture from twin screw extruder is added, weighting agent adds from the side loading mouth of twin screw extruder, extrude, granulation, obtained polypropylene composite.
Gained polypropylene composite is tested its tensile strength, modulus in flexure, Izod notched impact strength and laser-marking performance also by the results are shown in Table 4 according to testing method.
Following table 1-4 is component and the performance test data table of embodiment and comparative example in the present invention.
Table 1
Table 2
From upper table 1 with table 2, embodiment 1-10 and comparative example 1-10 contrasts, and can find out, uses laser absorbent and the promotor of scope of the present invention in embodiment 1-10; And in comparative example 1-10, be laser marking agent conventional at present: cupric phosphate and/or antimonous oxide.As can be seen from test result, when in promotor in embodiment 1-10 and laser absorbent consumption and comparative example 1-10, laser marking agent consumption is suitable, the polypropylene composite in embodiment 1-10, its laser-marking performance is better, and mechanical property is better.
In upper table 1 and table 2, embodiment 1, embodiment 2 and embodiment 4-8 and comparative example 1, comparative example 2 and comparative example 4-8 compare, can find out, when the consumption of laser absorbent in embodiment is 5-17 weight part, the laser-marking of obtained polypropylene composite is at least better, and the laser-marking of the polypropylene composite that the comparative example of correspondence obtains is for poor; Further when the consumption of laser absorbent in embodiment is 8-17 part, as well, and the laser-marking of the polypropylene composite that the comparative example of correspondence obtains is for poor for the laser-marking of obtained polypropylene composite.
Table 3
As shown in Table 3, embodiment 11 compares with comparative example 14, in polypropylene composite, adds the promotor of organic phosphate compound in embodiment 11, and the laser-marking of the polypropylene composite of its gained is better, and its mechanical property is better.
Contrasted as can be seen from embodiment 11-15 and comparative example 11-13, when laser absorbent is decabromodiphenyl oxide, TDE, brominated polystyrene, brominated epoxy resin or brominated triazine, laser absorbent is made compared to inorganic phosphate or metal oxide, the laser-marking performance of its polypropylene composite is better, and mechanical property is better.
Contrasted as can be seen from embodiment 11-13 and embodiment 14-15, when the preferred decabromodiphenyl oxide of laser absorbent of the present invention, TDE or brominated polystyrene, the laser-marking of the polypropylene composite of its gained is better.
Table 4
As shown in Table 4, embodiment 16 compares with comparative example 18, in polypropylene composite, adds the laser absorbent of TDE in embodiment 16, and the mechanical property of the polypropylene composite of its gained is suitable, but laser-marking performance is better.
Contrasted as can be seen from embodiment 16-18 and comparative example 15-17, when promotor is two (to tertiary butyl phenoxy group) sodium phosphate salts, 2,2'-methylene-bis (4,6-di-t-butyl) phenol sodium phosphate salt or 2, during 2'-methylene-bis (4,6-di-tert-butyl-phenyl) phosphalugel, compared to inorganic phosphate or metal oxide, the laser-marking performance of its polypropylene composite is better, and mechanical property is better.
The foregoing is only embodiments of the invention; not thereby the scope of the claims of the present invention is limited; every utilize description of the present invention to do equivalent structure or equivalent flow process conversion; or be directly or indirectly used in other relevant technical fields, be all in like manner included in scope of patent protection of the present invention.
Claims (9)
1. a polypropylene composite, is made up of the component of following weight part:
Polypropylene 30 ?100 parts;
Promotor 0.2 ?0.6 part;
Laser absorbent 5 ?30 parts;
Compatilizer 0 ?8 parts;
Weighting agent 0 ?40 parts;
Tinting pigment 0 ?0.8 part;
Oxidation inhibitor 0.1 ?1 part;
Processing aid 0.1 ?1 part;
Wherein, described laser absorbent is at least one in decabromodiphenyl oxide, brominated polystyrene, brominated epoxy resin or brominated triazine; Described promotor is two (to tertiary butyl phenoxy group) sodium phosphate salts, 2,2' ?methylene-bis (4,6 ?di-t-butyl) phenol sodium phosphate salt or 2,2' ?at least one in methylene-bis (4,6 ?di-tert-butyl-phenyl) phosphalugel.
2. polypropylene composite as claimed in claim 1, is characterized in that: described polypropylene 60 ?92 weight parts, described laser absorbent 5 ?17 weight parts, described weighting agent 10 ?31 weight parts, described compatilizer 3 ?8 weight parts.
3. polypropylene composite as claimed in claim 1 or 2, is characterized in that: described polypropylene composite does not comprise antimonous oxide, antimony peroxide or zinc borate.
4. polypropylene composite as claimed in claim 1 or 2, is characterized in that: described polypropylene is the combination of homo-polypropylene, block copolymerization polypropylene, atactic copolymerized polypropene or wherein at least two kinds of materials.
5. polypropylene composite as claimed in claim 1 or 2, is characterized in that: described compatilizer is the graftomer of polypropylene and unsaturated carboxylic acid or the graftomer of polypropylene and unsaturated carboxylic acid acid anhydrides.
6. polypropylene composite as claimed in claim 5, is characterized in that: described unsaturated carboxylic acid is maleic acid.
7. polypropylene composite as claimed in claim 1 or 2, is characterized in that: described weighting agent is at least one in talcum powder, calcium carbonate, barium sulfate, calcium sulfate, wollastonite, mica, glass microballon, glass fibre.
8. a preparation method for the polypropylene composite as described in any one of claim 1 to 7, is characterized in that:
In proportion the component except described weighting agent is placed in mixing machine mix and blend and obtains mixture, added by the main charging opening of gained mixture from twin screw extruder, the weighting agent of described ratio adds from the side loading mouth of twin screw extruder, extrudes, granulation, obtained polypropylene composite.
9. by the application of the polypropylene composite described in any one of claim 1 to 7, it is characterized in that: described polypropylene composite is applied to automobile, household electrical appliances and field of electronics.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201310059538.5A CN103289187B (en) | 2013-02-25 | 2013-02-25 | Polypropylene composite, its preparation method and application thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201310059538.5A CN103289187B (en) | 2013-02-25 | 2013-02-25 | Polypropylene composite, its preparation method and application thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN103289187A CN103289187A (en) | 2013-09-11 |
| CN103289187B true CN103289187B (en) | 2016-02-17 |
Family
ID=49090755
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201310059538.5A Active CN103289187B (en) | 2013-02-25 | 2013-02-25 | Polypropylene composite, its preparation method and application thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN103289187B (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114127170A (en) * | 2019-07-19 | 2022-03-01 | 利安德巴塞尔先进聚合物公司 | Laser-transparent composition and laser welding method |
| WO2022094791A1 (en) * | 2020-11-04 | 2022-05-12 | 上海荣腾包装服务有限公司 | Degradable stone-plastic polypropylene material and preparation method therefor |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102108177A (en) * | 2009-12-28 | 2011-06-29 | 江海波 | Resin composition and production method of plastic product of resin composition |
-
2013
- 2013-02-25 CN CN201310059538.5A patent/CN103289187B/en active Active
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102108177A (en) * | 2009-12-28 | 2011-06-29 | 江海波 | Resin composition and production method of plastic product of resin composition |
Also Published As
| Publication number | Publication date |
|---|---|
| CN103289187A (en) | 2013-09-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN102061071B (en) | Halogen-free flame retardant polyester with laser marking function and preparation method thereof | |
| CN104845361A (en) | Highly conductive thermoplastic plastic reinforced cooperatively by short carbon fiber and nano conductive carbon black/graphene and manufacturing method thereof | |
| CN102585348A (en) | Toughened conducting material and preparation method for toughened conducting material | |
| CN1103796C (en) | Low-temperature-resistant, halogen-free, flame-retardant polyolefin-based resin composition | |
| CN103289188B (en) | Polypropylene composite, its preparation method and application thereof | |
| CN102585367A (en) | Polypropylene composition supporting laser marking and preparation method and application thereof | |
| SK47599A3 (en) | Process for the production of coupling agent-treated inorganic particles and use thereof | |
| CN104419107A (en) | Polymer-based electromagnetic shielding material based on carbon fiber and graphene and preparation method of polymer-based electromagnetic shielding material | |
| CN103289187B (en) | Polypropylene composite, its preparation method and application thereof | |
| CN101962502A (en) | Multi-prevention EPDM rubber coating and preparation technology thereof | |
| CN103881187A (en) | Nano carbon fiber modified polyethylene material | |
| CN102477183A (en) | Enhanced antistatic material and preparation method thereof | |
| EP0062252A1 (en) | Polyolefin composition | |
| CN107513210A (en) | A kind of low smell electrodepositable polypropylene material and preparation method thereof | |
| CN103232632B (en) | Polypropylene composite, preparation method and application thereof | |
| CN108034126B (en) | Halogen-free flame-retardant polyolefin composite material and preparation method thereof | |
| CN103849076A (en) | Nanoscale antiflaming reinforced PS/PE (poly styrene/polyethylene) alloy material and preparation method thereof | |
| CN103265753B (en) | Polypropylene composite, preparation method and application thereof | |
| CN107384058A (en) | A kind of microcomputer harmonic elimination device acetal wire enamel | |
| DE19581920B4 (en) | Crystalline polyolefin resin composition and electrical insulating member containing this composition | |
| CN111363201B (en) | Composite material and preparation method thereof, nucleating agent and application | |
| CN108084556A (en) | A kind of electrolyte resistance polypropylene material with pearl effect and preparation method thereof | |
| CN110144105A (en) | A kind of outdoor optical cable fiber-dividing box, termination box, connector box nonmetallic composite | |
| KR20220092582A (en) | Modified carbon black, manufacturing method thereof, resin composition and copper clad laminate | |
| CN103881343A (en) | Nanometer flame-retardant reinforced PC/PBT alloy material and preparation method thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant |