CN107090176A - Modified nylon material and preparation method thereof - Google Patents
Modified nylon material and preparation method thereof Download PDFInfo
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- CN107090176A CN107090176A CN201710316672.7A CN201710316672A CN107090176A CN 107090176 A CN107090176 A CN 107090176A CN 201710316672 A CN201710316672 A CN 201710316672A CN 107090176 A CN107090176 A CN 107090176A
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- 239000000463 material Substances 0.000 title claims abstract description 102
- 239000004677 Nylon Substances 0.000 title claims abstract description 75
- 229920001778 nylon Polymers 0.000 title claims abstract description 75
- 238000002360 preparation method Methods 0.000 title claims abstract description 19
- 239000003063 flame retardant Substances 0.000 claims abstract description 31
- 239000012745 toughening agent Substances 0.000 claims abstract description 15
- 239000004952 Polyamide Substances 0.000 claims abstract description 14
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 14
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 14
- 229920002647 polyamide Polymers 0.000 claims abstract description 14
- 239000012752 auxiliary agent Substances 0.000 claims abstract description 12
- 238000001125 extrusion Methods 0.000 claims abstract description 12
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000000203 mixture Substances 0.000 claims description 25
- 239000000654 additive Substances 0.000 claims description 15
- 230000000996 additive effect Effects 0.000 claims description 15
- 230000000979 retarding effect Effects 0.000 claims description 12
- 229920002292 Nylon 6 Polymers 0.000 claims description 9
- 238000002844 melting Methods 0.000 claims description 7
- 230000008018 melting Effects 0.000 claims description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 3
- 239000006229 carbon black Substances 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 238000012545 processing Methods 0.000 claims description 3
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 claims description 3
- 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 2
- YUWBVKYVJWNVLE-UHFFFAOYSA-N [N].[P] Chemical compound [N].[P] YUWBVKYVJWNVLE-UHFFFAOYSA-N 0.000 claims description 2
- 229910000410 antimony oxide Inorganic materials 0.000 claims description 2
- 238000004040 coloring Methods 0.000 claims description 2
- 238000002485 combustion reaction Methods 0.000 claims description 2
- 239000002270 dispersing agent Substances 0.000 claims description 2
- 239000003112 inhibitor Substances 0.000 claims description 2
- 239000000314 lubricant Substances 0.000 claims description 2
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 claims description 2
- 239000003381 stabilizer Substances 0.000 claims description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 239000003245 coal Substances 0.000 abstract description 5
- 239000004753 textile Substances 0.000 abstract description 4
- 239000002861 polymer material Substances 0.000 abstract description 3
- 238000005469 granulation Methods 0.000 abstract description 2
- 230000003179 granulation Effects 0.000 abstract description 2
- 239000002216 antistatic agent Substances 0.000 abstract 2
- 239000002994 raw material Substances 0.000 abstract 1
- 238000005303 weighing Methods 0.000 abstract 1
- 238000012360 testing method Methods 0.000 description 6
- 238000005452 bending Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 238000012986 modification Methods 0.000 description 5
- 230000004048 modification Effects 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 125000003003 spiro group Chemical group 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 230000005611 electricity Effects 0.000 description 2
- 229920006351 engineering plastic Polymers 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 239000011236 particulate material Substances 0.000 description 2
- 238000011056 performance test Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 240000002853 Nelumbo nucifera Species 0.000 description 1
- 235000006508 Nelumbo nucifera Nutrition 0.000 description 1
- 235000006510 Nelumbo pentapetala Nutrition 0.000 description 1
- 244000178289 Verbascum thapsus Species 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229920003231 aliphatic polyamide Polymers 0.000 description 1
- 150000001408 amides Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 239000000686 essence Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000004079 fireproofing Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/02—Polyamides derived from omega-amino carboxylic acids or from lactams thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/92—Measuring, controlling or regulating
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/06—Polyamides derived from polyamines and polycarboxylic acids
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92504—Controlled parameter
- B29C2948/92514—Pressure
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92504—Controlled parameter
- B29C2948/92704—Temperature
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/38—Boron-containing compounds
- C08K2003/387—Borates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/017—Additives being an antistatic agent
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/02—Flame or fire retardant/resistant
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/04—Antistatic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/06—Polymer mixtures characterised by other features having improved processability or containing aids for moulding methods
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention belongs to the technical field of high polymer materials, and particularly relates to a modified nylon material and a preparation method thereof. The modified nylon material comprises: 49-64% of polyamide; 15-18% of flame retardant; 5-7% of flame-retardant synergist; 10-13% of a toughening agent; 5-20% of antistatic agent; 0.2 to 0.4 percent of antioxidant; 0.1 to 1 percent of other auxiliary agents. The preparation method comprises the following steps: weighing raw materials of each component; mixing polyamide, flame retardant synergist, antistatic agent, antioxidant and other auxiliaries to obtain a mixed material; and (3) feeding the mixed material into a main feeding hopper of a double-screw extruder, feeding the toughening agent into a side feeding port of the double-screw extruder, and performing melt extrusion granulation. The modified nylon material has antistatic and flame retardant properties, ensures the mechanical properties of the material, achieves the optimal comprehensive properties, is suitable for IC parts and some precise instruments, and is widely applied to industries such as coal mines, textile equipment, electronic appliances and the like.
Description
Technical field
The invention belongs to technical field of polymer materials, and in particular to a kind of modified nylon materials and preparation method thereof.
Background technology
Polyamide is commonly called as nylon (Nylon), and English name Polyamide (abbreviation PA) is containing repetition on molecular backbone
Amide group-[NHCO]-thermoplastic resin general name, including aliphatic PA, aliphatic-aromatic race PA and aromatic series PA.Wherein fat
Fat race PA is wide in variety, and yield is big, is widely used, and it is named depending on the specific carbon number of synthon.PA's is various in style,
There are PA6, PA66, PA46, PA610, PA612 etc..
The PA6 (nylon 6) of high comprehensive performance is that engineering plastics develop earliest kind, is described as epoch-making engineering plastic
Material.PA has excellent wearability, impact resistance and self lubricity;But nylon 6 is all tool as most of high polymer materials
There is the dielectric of good electrical insulation capability, its sheet resistance is general 1014~1015Ω, electric conductivity is much smaller than metal material,
Easy static electricity gathered lotus after contacting or rubbing with other materials.The negative interaction that accumulation of static electricity is brought be hinder normal production and
Work, or even can set off an explosion and fire.Therefore in the specific work environments of the industries such as underground coal mine, textile equipment, electronic apparatus
Or under dynamic operating condition, it is desirable to anti-static function is also presented while with higher mechanical property in the product of nylon 6, i.e.,
Sheet resistance is down to 1011~1012Ω or volume resistance reach 1011Ω cm, to meet the property requirements used.But because
A large amount of fire retardant, the additions of antistatic additive so that PA6 mechanical property is substantially reduced, and strengthens PA6 because of the " candle wick of fiber
Effect " makes its more easy firing.So this is accomplished by so that nylon ensures the mechanical property of nylon again while anti-electrostatic fire retardant
Can, current material can not meet the requirement.
The content of the invention
It is an object of the invention to the above-mentioned deficiency for overcoming prior art, there is provided a kind of modified nylon materials and its preparation side
Method, it is intended to the problems such as solving the technology that the mechanical property and antistatic fire protecting performance of existing nylon material cannot be balanced.
For achieving the above object, the technical solution adopted by the present invention is as follows:
One aspect of the present invention provides a kind of modified nylon materials, is counted using the gross mass of the modified nylon materials as 100%,
The modified nylon materials include the composition of following weight/mass percentage composition:
Another aspect of the present invention provides a kind of preparation method of modified nylon materials, and the preparation method comprises the following steps:
Each component materials are weighed respectively according to the composition and its content contained by above-mentioned modified nylon materials;
By the polyamide, the fire retardant, the fire retarding synergist, the antistatic additive, the antioxidant and described
Other auxiliary agent mixed processings obtain mixed material;
In the main feed hopper that the mixed material is sent into double screw extruder, and toughener feeding is described double
In the side spout of screw extruder, granulated through melting extrusion.
In the modified nylon materials that the present invention is provided, it is fire-retardant that fire retardant and fire retarding synergist have modified nylon materials
Property, toughener further improves its tensile strength, and antistatic additive makes the modified nylon materials have anti-electrostatic fire retardant, changes
Property nylon material in each composition and content between fully merge, by synergy, make the modified nylon materials with anti-
Ensure its mechanical property while electrostatic is fire-retardant again, combination property is optimal, be applicable to IC parts and some accurate instrument
Device, can be widely applied to the industries such as coal mine, textile equipment, electronic apparatus.
The preparation method for the modified nylon materials that the present invention is provided, simple for process, cost is low.This final obtained hair
Bright modified nylon materials ensure its mechanical property again while with anti-electrostatic fire retardant, and combination property is optimal.
Embodiment
In order that technical problems, technical solutions and advantageous effects to be solved by the present invention are more clearly understood, below in conjunction with
Embodiment, the present invention will be described in further detail.It should be appreciated that specific embodiment described herein is only to explain
The present invention, is not intended to limit the present invention.
On the one hand, the embodiments of the invention provide a kind of modified nylon materials, using the gross mass of the modified nylon materials as
100% meter, it includes the composition of following weight/mass percentage composition:
Fully merged between each composition and content in modified nylon materials, by synergy, make the modification of nylon material
Material ensure its mechanical property again while with anti-electrostatic fire retardant, combination property is optimal, be applicable to IC parts with
Some precision instruments, can be widely applied to the industries such as coal mine, textile equipment, electronic apparatus.
Specifically, in the modified nylon materials of the embodiment of the present invention, the content of polyamide is 49-64%, is specifically as follows
49%th, 54%, 59%, 60%, 64%.Preferably, polyamide is at least one of PA6, PA66 and PA610.
Specifically, in the modified nylon materials of the embodiment of the present invention, the content of fire retardant is 15-18%, is specifically as follows
15%th, 16%, 17%, 18%.The content of fire retarding synergist is 5-7%, is specifically as follows 5%, 6%, 7%.In the content model
Interior fire retardant and fire retarding synergist is enclosed, the modified nylon materials fire resistance of the embodiment of the present invention is significantly improved.Preferably, should
Fire retardant includes at least one of phosphorus-nitrogen containing flame retardant, nitrogenated flame retardant and red phosphorus combustion inhibitor, and red phosphorus is selected in the present embodiment, hinders
Firing synergist includes being at least one of antimony oxide and Firebrake ZB, selects Firebrake ZB in the present embodiment.It is preferred that fire retardant
And fire retarding synergist, the modified nylon materials fire resistance of the present embodiment is reached most preferably.
Specifically, in the modified nylon materials of the embodiment of the present invention, the content of toughener is 10-13%, is specifically as follows
10%th, 11%, 12%, 13%;Toughener in the content range, significantly improves the modified nylon materials of the embodiment of the present invention
Tensile resistance.Preferably, the toughener includes at least one of LDPE-g-MAH and SEBS-g-MAH.It is preferred that toughener
The modified nylon materials tensile resistance of the present embodiment is set to reach most preferably.
Specifically, in the modified nylon materials of the embodiment of the present invention, the content of antistatic additive is 5-20%, is specifically as follows
5%th, 10%, 15%, 20%, the antistatic additive in the content range significantly improves the modification of nylon material of the embodiment of the present invention
The anti-electrostatic fire retardant of material.Preferably, the antistatic additive is acetylene carbon black.Superconduct the selection of acetylene carbon black, make modification of nylon
The anti-electrostatic fire retardant of material reaches most preferably.
Specifically, in the modified nylon materials of the embodiment of the present invention, the content of antioxidant is 0.2-0.4%, specifically can be with
For 0.2%, 0.3%, 0.4%;Antioxidant in the content range, significantly prevents the modified nylon materials of the embodiment of the present invention
Aging, further improve its service life.Preferably, the antioxidant is included at least one in antioxidant 1010 and irgasfos 168
Kind.It is preferred that antioxidant make the service life of modified nylon materials most long.
Specifically, in the modified nylon materials of the embodiment of the present invention, the content of other auxiliary agents is 0.1-1%, concretely
0.1%th, 0.3%, 0.5%, 1%.Preferably, other auxiliary agents are included in lubricant, stabilizer, colouring agent, dispersant at least
It is a kind of.Which kind of auxiliary agent can be specifically selected according to the actual requirements.
On the other hand, the embodiment of the present invention also provides a kind of preparation method of modified nylon materials.The preparation method includes
Following steps:
S01:Each component materials are weighed respectively according to the composition and its content contained by above-mentioned modified nylon materials;
S02:By above-mentioned polyamide, fire retardant, fire retarding synergist, antistatic additive, antioxidant and other auxiliary agent mixed processings
Obtain mixed material;
S03:In the main feed hopper that said mixture material is sent into double screw extruder, and above-mentioned toughener feeding is double
In the side spout of screw extruder, granulated through melting extrusion.
The preparation method for the modified nylon materials that the present invention is provided, simple for process, cost is low.This final obtained hair
Bright modified nylon materials ensure its mechanical property again while with anti-electrostatic fire retardant, and combination property is optimal.
Preferably, in above-mentioned steps S03, the technological parameter of the double screw extruder is:One 240 DEG C -280 DEG C of area's temperature,
Two 250 DEG C -290 DEG C of area's temperature, three 250 DEG C -290 DEG C of area's temperature, four 240 DEG C -280 DEG C of area's temperature, 250 DEG C -300 DEG C of head,
Residence time 1min-2min, pressure is 12MPa-18MPa.Modified nylon materials performance reaches made from the preferred technological parameter
To optimal.
It is of the invention successively to carry out test of many times, now lift A partial experiment result further detailed as reference pair invention progress
Thin description, is described in detail with reference to specific embodiment.
Embodiment 1
A kind of modified nylon materials, it is formulated the embodiment 1 being shown in Table in 1.The preparation method of the modified nylon materials includes
Following steps:
S11:It is former that each composition is weighed respectively according to the composition and its content contained by the modified nylon materials of embodiment 1 in table 1
Material.
S12:Above-mentioned polyamide, fire retardant, fire retarding synergist, antistatic additive, antioxidant and other auxiliary agents are put into stirring
Bucket carries out being sufficiently mixed 15 minutes to obtain mixed material.
S13:In the main feed hopper that said mixture material is sent into double screw extruder, and above-mentioned toughener feeding is double
In the side spout of screw extruder, granulated through melting extrusion.Wherein, the technological parameter of the double screw extruder is:Screw rod is straight
Footpath is 35mm, and the ratio of spiro rod length and diameter is set as 36, and extrusion temperature is respectively 240 DEG C of area's temperature, two area's temperature 250
DEG C, three 240 DEG C of area's temperature, four 230 DEG C of area's temperature, 245 DEG C of head temperature, residence time 1-2min, pressure is 13MPa.
Embodiment 2
A kind of modified nylon materials, it is formulated the embodiment 2 being shown in Table in 1.The preparation method of the modified nylon materials includes
Following steps:
S21:It is former that each composition is weighed respectively according to the composition and its content contained by the modified nylon materials of embodiment 2 in table 1
Material.
S22:Above-mentioned polyamide, fire retardant, fire retarding synergist, antistatic additive, antioxidant and other auxiliary agents are put into stirring
Bucket carries out being sufficiently mixed 15 minutes to obtain mixed material.
S23:In the main feed hopper that said mixture material is sent into double screw extruder, and above-mentioned toughener feeding is double
In the side spout of screw extruder, granulated through melting extrusion.Wherein, the technological parameter of the double screw extruder is:Screw rod is straight
Footpath is 35mm, and the ratio of spiro rod length and diameter is set as 36, and extrusion temperature is respectively 240 DEG C of area's temperature, two area's temperature 250
DEG C, three 240 DEG C of area's temperature, four 230 DEG C of area's temperature, 245 DEG C of head temperature, residence time 1-2min, pressure is 13MPa.
Embodiment 3
A kind of modified nylon materials, it is formulated the embodiment 3 being shown in Table in 1.The preparation method of the modified nylon materials includes
Following steps:
S31:It is former that each composition is weighed respectively according to the composition and its content contained by the modified nylon materials of embodiment 3 in table 1
Material.
S32:Above-mentioned polyamide, fire retardant, fire retarding synergist, antistatic additive, antioxidant and other auxiliary agents are put into stirring
Bucket carries out being sufficiently mixed 15 minutes to obtain mixed material.
S33:In the main feed hopper that said mixture material is sent into double screw extruder, and above-mentioned toughener feeding is double
In the side spout of screw extruder, granulated through melting extrusion.Wherein, the technological parameter of the double screw extruder is:Screw rod is straight
Footpath is 35mm, and the ratio of spiro rod length and diameter is set as 36, and extrusion temperature is respectively 240 DEG C of area's temperature, two area's temperature 250
DEG C, three 240 DEG C of area's temperature, four 230 DEG C of area's temperature, 245 DEG C of head temperature, residence time 1-2min, pressure is 13MPa.
Embodiment 4
A kind of modified nylon materials, it is formulated the embodiment 4 being shown in Table in 1.The preparation method of the modified nylon materials includes
Following steps:
S41:It is former that each composition is weighed respectively according to the composition and its content contained by the modified nylon materials of embodiment 4 in table 1
Material.
S42:Above-mentioned polyamide, fire retardant, fire retarding synergist, antistatic additive, antioxidant and other auxiliary agents are put into stirring
Bucket carries out being sufficiently mixed 15 minutes to obtain mixed material.
S43:In the main feed hopper that said mixture material is sent into double screw extruder, and above-mentioned toughener feeding is double
In the side spout of screw extruder, granulated through melting extrusion.Wherein, the technological parameter of the double screw extruder is:Screw rod is straight
Footpath is 35mm, and the ratio of spiro rod length and diameter is set as 36, and extrusion temperature is respectively 240 DEG C of area's temperature, two area's temperature 250
DEG C, three 240 DEG C of area's temperature, four 230 DEG C of area's temperature, 245 DEG C of head temperature, residence time 1-2min, pressure is 13MPa.
Table 1
Performance test:
The particulate material that granulation is completed by above-described embodiment 1- embodiments 4 is dried in 110 DEG C of convection oven in advance
3-5 hours, dried particulate material is then subjected to injection moulding sample preparation, injection mold temperature control on injection machine again
System is at 150 DEG C or so.Performance test is carried out by the following method, and resulting test result is as shown in table 2.
Tensile strength test is carried out by ASTM D638, and specimen size is 165 × 19 × 3.2mm, and draw speed is 50mm/
min;Bending property test is carried out by ASTM D790, and specimen size is 127 × 12.7 × 3.2, and rate of bending is 20mm/min,
Span is 64mm;Simple beam impact strength is carried out by ASTM D256, and specimen size is 63.5 × 12.7 × 3.2mm, notch size
For 1/3rd of sample thickness;Fire resistance is carried out by UL94 methods, and batten thickness is about 3.2mm.
Tensile strength of the comprehensive mechanical property as obtained by test, elongation at break, bending modulus and impact strength
Numerical value is judged;The fire resistance of material is judged by UL94 standard.Antistatic effect is tested with ammeter.
Table 2
Test event | Embodiment 1 | Embodiment 2 | Embodiment 3 | Embodiment 4 |
Tensile strength (Mpa) | 60 | 45 | 35 | 25 |
Elongation at break (%) | 70 | 60 | 50 | 40 |
Bending strength (Mpa) | 100 | 70 | 40 | 30 |
Bending modulus (Mpa) | 2000 | 1500 | 1100 | 1000 |
Notch impact strength (J/M) | 140 | 120 | 110 | 90 |
Anti-flammability (3.2mm) | V0 | V0 | V0 | V0 |
Conductive (Ω) | 1012(non-conductive) | 1011 | 108 | 105 |
It was found from the data of table 2:In embodiment 1-4, with the increase of antistatic additive, the conduction of the modified nylon materials
Performance is also gradually stepped up.It is overall apparently, antistatic effect can be reached in the case of 15 parts or so of antistatic additive, while the modification
Nylon material physical property is also retained.Coal mine, spinning is fully achieved in the modified nylon materials performance that the present embodiment is provided
The industries such as equipment, electronic apparatus are knitted, and material is free of halogen, will not release harmful gas because of its decomposition in use
Body, pollution-free to air and water etc., its cost is even lower than halogen fire proofing, has broad application prospects.
The foregoing is merely illustrative of the preferred embodiments of the present invention, is not intended to limit the invention, all essences in the present invention
Any modifications, equivalent substitutions and improvements made within refreshing and principle etc., should be included in the scope of the protection.
Claims (10)
1. a kind of modified nylon materials, it is characterised in that counted using the gross mass of the modified nylon materials as 100%, described to change
Property nylon material includes the composition of following weight/mass percentage composition:
2. modified nylon materials as claimed in claim 1, it is characterised in that the polyamide is in PA6, PA66 and PA610
At least one.
3. modified nylon materials as claimed in claim 1, it is characterised in that the fire retardant includes phosphorus-nitrogen containing flame retardant, nitrogen
At least one of flame retardant and red phosphorus combustion inhibitor.
4. modified nylon materials as claimed in claim 1, it is characterised in that the fire retarding synergist includes being antimony oxide
At least one of with Firebrake ZB.
5. modified nylon materials as claimed in claim 1, it is characterised in that the toughener include LDPE-g-MAH and
At least one of SEBS-g-MAH.
6. modified nylon materials as claimed in claim 1, it is characterised in that the antistatic additive is acetylene carbon black.
7. modified nylon materials as claimed in claim 1, it is characterised in that the antioxidant includes antioxidant 1010 and antioxygen
At least one of agent 168.
8. modified nylon materials as claimed in claim 1, it is characterised in that other described auxiliary agents comprising lubricant, stabilizer,
At least one of colouring agent, dispersant.
9. a kind of preparation method of modified nylon materials, it is characterised in that comprise the following steps:
It is former that each composition is weighed respectively according to the composition and its content contained by any described modified nylon materials of claim 1-8
Material;
By the polyamide, the fire retardant, the fire retarding synergist, the antistatic additive, the antioxidant and it is described other
Auxiliary agent mixed processing obtains mixed material;
In the main feed hopper that the mixed material is sent into double screw extruder, and the toughener is sent into the twin-screw
In the side spout of extruder, granulated through melting extrusion.
10. the preparation method of modified nylon materials as claimed in claim 9, it is characterised in that the double screw extruder
Technological parameter is:One 240 DEG C -280 DEG C of area's temperature, two 250 DEG C -290 DEG C of area's temperature, three 250 DEG C -290 DEG C of area's temperature, four area's temperature
240 DEG C -280 DEG C of degree, 250 DEG C -300 DEG C of head, residence time 1min-2min, pressure is 12MPa-18MPa.
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102863788A (en) * | 2012-09-28 | 2013-01-09 | 合肥杰事杰新材料股份有限公司 | Low-surface-resistance high-glass-fiber reinforced flame-retardant nylon resin composition and preparation method thereof |
CN103073886A (en) * | 2012-12-25 | 2013-05-01 | 安徽科聚新材料有限公司 | Nylon 66 composite material, preparation method thereof and electronic device |
CN104419198A (en) * | 2013-08-20 | 2015-03-18 | 上海杰事杰新材料(集团)股份有限公司 | Flame-retardant anti-static continuous long-glass-fiber-reinforced high-temperature-resistant nylon composite material and preparation method thereof |
CN105504791A (en) * | 2015-12-29 | 2016-04-20 | 中国石油化工股份有限公司 | Environment-friendly flame-retardant antistatic nylon composite and preparation method thereof |
-
2017
- 2017-05-08 CN CN201710316672.7A patent/CN107090176A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102863788A (en) * | 2012-09-28 | 2013-01-09 | 合肥杰事杰新材料股份有限公司 | Low-surface-resistance high-glass-fiber reinforced flame-retardant nylon resin composition and preparation method thereof |
CN103073886A (en) * | 2012-12-25 | 2013-05-01 | 安徽科聚新材料有限公司 | Nylon 66 composite material, preparation method thereof and electronic device |
CN104419198A (en) * | 2013-08-20 | 2015-03-18 | 上海杰事杰新材料(集团)股份有限公司 | Flame-retardant anti-static continuous long-glass-fiber-reinforced high-temperature-resistant nylon composite material and preparation method thereof |
CN105504791A (en) * | 2015-12-29 | 2016-04-20 | 中国石油化工股份有限公司 | Environment-friendly flame-retardant antistatic nylon composite and preparation method thereof |
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