CN105348520A - Semi-aromatic polyamide and synthesis method thereof - Google Patents
Semi-aromatic polyamide and synthesis method thereof Download PDFInfo
- Publication number
- CN105348520A CN105348520A CN201510890781.0A CN201510890781A CN105348520A CN 105348520 A CN105348520 A CN 105348520A CN 201510890781 A CN201510890781 A CN 201510890781A CN 105348520 A CN105348520 A CN 105348520A
- Authority
- CN
- China
- Prior art keywords
- stirring
- monomer
- polymerization reactor
- add
- type polymerization
- 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.)
- Granted
Links
- 229920006012 semi-aromatic polyamide Polymers 0.000 title claims abstract description 43
- 238000001308 synthesis method Methods 0.000 title abstract 2
- 229920006149 polyester-amide block copolymer Polymers 0.000 claims abstract description 46
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 20
- 238000006116 polymerization reaction Methods 0.000 claims description 76
- 239000000178 monomer Substances 0.000 claims description 58
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 55
- 239000000203 mixture Substances 0.000 claims description 45
- 238000006243 chemical reaction Methods 0.000 claims description 41
- 229910052757 nitrogen Inorganic materials 0.000 claims description 35
- -1 propyl titanate Chemical compound 0.000 claims description 25
- GUOSQNAUYHMCRU-UHFFFAOYSA-N 11-Aminoundecanoic acid Chemical compound NCCCCCCCCCCC(O)=O GUOSQNAUYHMCRU-UHFFFAOYSA-N 0.000 claims description 24
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 22
- 239000007789 gas Substances 0.000 claims description 22
- 238000010189 synthetic method Methods 0.000 claims description 21
- 238000013022 venting Methods 0.000 claims description 19
- 230000001276 controlling effect Effects 0.000 claims description 15
- 238000007599 discharging Methods 0.000 claims description 15
- 230000001105 regulatory effect Effects 0.000 claims description 15
- 238000003756 stirring Methods 0.000 claims description 15
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 14
- 229910052901 montmorillonite Inorganic materials 0.000 claims description 14
- 239000000376 reactant Substances 0.000 claims description 14
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 13
- 238000001291 vacuum drying Methods 0.000 claims description 13
- YQLZOAVZWJBZSY-UHFFFAOYSA-N decane-1,10-diamine Chemical compound NCCCCCCCCCCN YQLZOAVZWJBZSY-UHFFFAOYSA-N 0.000 claims description 12
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 11
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 11
- JBFHTYHTHYHCDJ-UHFFFAOYSA-N gamma-caprolactone Chemical compound CCC1CCC(=O)O1 JBFHTYHTHYHCDJ-UHFFFAOYSA-N 0.000 claims description 10
- 150000003609 titanium compounds Chemical class 0.000 claims description 10
- 238000010792 warming Methods 0.000 claims description 9
- 235000019256 formaldehyde Nutrition 0.000 claims description 8
- 238000010438 heat treatment Methods 0.000 claims description 8
- 239000013589 supplement Substances 0.000 claims description 8
- 229910052786 argon Inorganic materials 0.000 claims description 7
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 claims description 7
- 238000007334 copolymerization reaction Methods 0.000 claims description 7
- 239000011261 inert gas Substances 0.000 claims description 7
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 7
- HMOZDINWBHMBSQ-UHFFFAOYSA-N 2-[3-(4,5-dihydro-1,3-oxazol-2-yl)phenyl]-4,5-dihydro-1,3-oxazole Chemical compound O1CCN=C1C1=CC=CC(C=2OCCN=2)=C1 HMOZDINWBHMBSQ-UHFFFAOYSA-N 0.000 claims description 6
- 239000003112 inhibitor Substances 0.000 claims description 6
- 230000003647 oxidation Effects 0.000 claims description 6
- 238000007254 oxidation reaction Methods 0.000 claims description 6
- 230000007704 transition Effects 0.000 claims description 5
- 238000010521 absorption reaction Methods 0.000 abstract description 3
- 238000000034 method Methods 0.000 description 14
- 230000015572 biosynthetic process Effects 0.000 description 12
- 238000012546 transfer Methods 0.000 description 9
- 239000002994 raw material Substances 0.000 description 8
- 238000003786 synthesis reaction Methods 0.000 description 8
- 230000008569 process Effects 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 238000012545 processing Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
- 150000001408 amides Chemical class 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 239000004952 Polyamide Substances 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229920000106 Liquid crystal polymer Polymers 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 239000004734 Polyphenylene sulfide Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000009795 derivation Methods 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 229920006351 engineering plastic Polymers 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229920006128 poly(nonamethylene terephthalamide) Polymers 0.000 description 2
- 238000006068 polycondensation reaction Methods 0.000 description 2
- 229920000069 polyphenylene sulfide Polymers 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 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 description 1
- ZEMPKEQAKRGZGQ-AAKVHIHISA-N 2,3-bis[[(z)-12-hydroxyoctadec-9-enoyl]oxy]propyl (z)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCCC(O)C\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CC(O)CCCCCC)COC(=O)CCCCCCC\C=C/CC(O)CCCCCC ZEMPKEQAKRGZGQ-AAKVHIHISA-N 0.000 description 1
- 125000003504 2-oxazolinyl group Chemical group O1C(=NCC1)* 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 240000002853 Nelumbo nucifera Species 0.000 description 1
- 235000006508 Nelumbo nucifera Nutrition 0.000 description 1
- 235000006510 Nelumbo pentapetala Nutrition 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 210000001072 colon Anatomy 0.000 description 1
- 229920006147 copolyamide elastomer Polymers 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 229920006111 poly(hexamethylene terephthalamide) Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/36—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino acids, polyamines and polycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/44—Polyester-amides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/48—Polymers modified by chemical after-treatment
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
- C08K5/3435—Piperidines
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- General Chemical & Material Sciences (AREA)
- Polyamides (AREA)
Abstract
The invention relates to semi-aromatic polyamide and a synthesis method thereof. The semi-aromatic polyamide has the structure shown in the formula I (shown in the description); in the formula I, a is equal to 10-200, b is equal to 10-200, c is equal to 10-100 and R is polyesteramide. The semi-aromatic polyamide has a relatively high mechanical property, relatively high heat resistance, low water absorption, excellent processability and biologically-derived characteristics, and can be applied to the fields of electronics and electrical appliances, LEDs, automobiles, aerospace, military and the like.
Description
Technical field
The present invention relates to Material Field, particularly relate to semiaromatic polyamide composition and synthetic method thereof.
Background technology
In recent years, in order to meet the more high performance requirement in fields such as electronics, electrical equipment, automobiles, particularly along with surface mounting technique (SurfaceMountTechnology, be called for short SMT) development, common thermostability engineering plastic polyphenylene sulfide (PPS) and the thermotolerance of liquid crystalline polymers (LCP) can not meet its requirement completely, and therefore developing the higher engineering plastics of thermotolerance just becomes inevitable.
Semiaromatic polyamide composition is normally by diacid or the diamines of aliphatic diamines or diacid and band aromatic nucleus, obtain through polycondensation, owing to having imported aromatic nucleus on polyamide molecule main chain, its thermotolerance and mechanical property are improved, and water-intake rate is reduced, have good superiority of effectiveness, it is mainly used in automobile and electric and electronic industry.Industrialized semiaromatic polyamide composition mainly contains polyamide 6 T (multipolymer), polyamide 9T, polymeric amide 10T etc.But the fusing point of polymeric amide 10T resin is about 320 DEG C, and itself and decomposition temperature are more or less the same, and processing temperature narrow limits, easily causes polymer unwinds in the course of processing, reduce its melt temperature so usually adopt with the method for other copolyamide.
Solid state polymerization (SolidstatePolymerization) refers to the polyreaction that solid (or crystalline phase) monomer occurs below its fusing point, or the polyreaction of carrying out more than monomer fusing point but below the melt temperature of the polymkeric substance formed.Due to solid state polymerization generally below the fusing point of prepolymer 15 ~ 30 DEG C carry out, its speed of reaction is comparatively slow, the reaction times is longer, and the production process of solid state polymerization is many, flow process is complicated, require higher to device parameter, reaction also needs to ensure that the proportioning of functional group is close to 1:1, and the thickening stage needs vacuum or air-flow to accelerate the discharge of small molecular by product, thus improves the molecular weight of polycondensation product, therefore, above condition limits the large-scale promotion of solid state polymerization.Melt polymerization (MeltPolymerization) refer to monomer and polymkeric substance be all in molten state under polymerization process, the method operational path is simple, can continuous seepage, also can batch production.Reaction needed is at high temperature carried out, and the reaction times is shorter, and the by product such as water molecules is discharged easily.At present, in prior art, some researchs are done to the synthesis of semiaromatic polyamide composition, the polymerisate that such as Chinese patent CN102153741A discloses a kind of homopolymer of Long carbon chain semiaromatic heat resistant polyamide and the synthetic method of multipolymer and obtains, this polymerisate is mainly obtained by the method for solid state polymerization; Chinese patent CN103360599A discloses a kind of semi-aromatic and fatty polyamide block copolymer, wherein the mole percent level of semiaromatic polyamide composition block is 40% ~ 99%, the mole percent level of fatty polyamide block is 1 ~ 60%, and this polymerisate is mainly obtained by the method for solid state polymerization; Chinese patent CN101948619A discloses a kind of poly-paraphenylene terephthalamide's nonamethylene diamine material and preparation method thereof; Chinese patent CN1106842A discloses polyamide 9T, 9M-T and preparation method thereof.
Summary of the invention
The object of the present invention is to provide a kind of higher mechanical property and resistance toheat, low water absorption, processing characteristics is excellent and have the semiaromatic polyamide composition of biogenetic derivation, can be applicable to field of electronics, LED field, automotive field, aerospace and military industry field etc.
For achieving the above object, the present invention adopts following scheme:
A kind of semiaromatic polyamide composition, it has as shown in the formula I structure:
In formula I, a=10 ~ 200, b=10 ~ 200, c=10 ~ 100, R is polyesteramide, and it has as shown in the formula II structure:
In formula II, x=10 ~ 200, y=10 ~ 200, z=10 ~ 100;
Described semiaromatic polyamide composition is formed by monomer 1 and polyesteramide copolymerization, described monomer 1 for mol ratio be decamethylene diamine, terephthalic acid, the 11-aminoundecanoic acid of 1:1:0.05 ~ 0.2, described polyesteramide add-on is 1 ~ 8% of described monomer 1 gross weight.
Wherein in some embodiments, the add-on of described polyesteramide is 2 ~ 6% of described monomer 1 gross weight.
Wherein in some embodiments, the limiting viscosity of described semiaromatic polyamide composition is 0.7 ~ 1.0dL/g, second-order transition temperature T
g>=100 DEG C, melt temperature T
mit is 295 ~ 305 DEG C.
Wherein in some embodiments, described polyesteramide is formed by monomer 2 copolymerization, described monomer 2 for mol ratio be the 11-aminoundecanoic acid of 1:0.5 ~ 1:0.1 ~ 0.4,6-caprolactone and 2,2'-(1,3-phenylene)-bisoxazoline.
Wherein in some embodiments, described polyesteramide is obtained by following synthetic method: the described monomer 2 after vacuum-drying joins in stirring-type polymerization reactor by (1), add simultaneously the titanium compound of 0.1 ~ 2% of described monomer 2 gross weight as catalyzer, add suitable quantity of water (medium of mass-and heat-transfer); Then vacuumize 3 ~ 10min, logical rare gas element 3 ~ 10min, so circulate 5 ~ 10 times, in the environment under making reactant be present in protection of inert gas, controlling system pressure in described stirring-type polymerization reactor is 0.1 ~ 0.5MPa;
(2) 240 ~ 260 DEG C are heated to by airtight for described stirring-type polymerization reactor, the stirring velocity of described stirring-type polymerization reactor is regulated to be 0 ~ 100r/min, wherein, when described stirring-type polyreaction actuator temperature reaches 210 DEG C, venting is to 1.6MPa, and maintain pressure at 1.6MPa, react after 0.5 ~ 4 hour, exit to normal pressure, reaction is continued after 0.5 ~ 4 hour at 240 ~ 260 DEG C, constant temperature continues to vacuumize 0.1 ~ 2 hour, and reaction terminates, the topping up when discharging;
In above-mentioned steps, described rare gas element is nitrogen or argon gas; Described titanium compound is one or more the mixture in tetrabutyl titanate, sec.-propyl titanic acid ester, propyl titanate, propenyl titanic acid ester.
Another object of the present invention is to provide the synthetic method of above-mentioned semiaromatic polyamide composition, comprises the following steps:
(1) described monomer 1 is joined in stirring-type polymerization reactor, add described polyesteramide, molecular weight regulator, oxidation inhibitor, water (medium of mass-and heat-transfer) simultaneously; Then vacuumize 3 ~ 10min, logical rare gas element 3 ~ 10min, so circulate 5 ~ 10 times, in the environment under making reactant be present in protection of inert gas, controlling system pressure in described stirring-type polymerization reactor is 0.1 ~ 0.5MPa; Described monomer 1 for mol ratio be decamethylene diamine, terephthalic acid, the 11-aminoundecanoic acid of 1:1:0.05 ~ 0.2, described polyesteramide add-on is add described monomer 1 gross weight 1 ~ 8%; Described polyesteramide is formed by monomer 2 copolymerization, described monomer 2 for mol ratio be 11-aminoundecanoic acid, 6-caprolactone, 2,2'-(1,3-phenylene)-bisoxazoline of 1:0.5 ~ 1:0.1 ~ 0.4;
(2) 270 ~ 285 DEG C are heated to by airtight for described stirring-type polymerization reactor, the stirring velocity of described stirring-type polymerization reactor is regulated to be 0 ~ 100r/min, wherein, when described stirring-type polyreaction actuator temperature reaches 215 DEG C, venting is to 2.0MPa, and maintain pressure at 2.0MPa, react after 0.5 ~ 4 hour, venting is to normal pressure, continue reaction at being warming up to 306 ~ 325 DEG C after 0.5 ~ 4 hour simultaneously, constant temperature continues to vacuumize 0.1 ~ 2 hour, and reaction terminates, the topping up when discharging;
In above-mentioned steps, described rare gas element is nitrogen or argon gas.
Before reaction, logical rare gas element object reduces the probability of side reaction generation; The object vacuumized in reaction process is the water removing producing in polyreaction, is conducive to polyreaction forward and carries out.
Wherein in some embodiments, above-mentioned synthetic method comprises the following steps:
(1) the described monomer 1 after vacuum-drying is joined in stirring-type polymerization reactor, add described polyesteramide, molecular weight regulator, oxidation inhibitor, water simultaneously; Then vacuumize 4 ~ 6min, logical nitrogen 4 ~ 6min, so circulate 5 ~ 7 times, in the environment under making reactant be present in nitrogen protection, controlling system pressure in described stirring-type polymerization reactor is 0.2 ~ 0.3MPa;
(2) in 2 ~ 4 hours by described airtight constant-speed heating to 272 ~ 280 DEG C of stirring-type polymerization reactor, the stirring velocity of described stirring-type polymerization reactor is regulated to be 30 ~ 50r/min, wherein, when described stirring-type polyreaction actuator temperature reaches 215 DEG C, venting is to 2.0MPa, and maintain pressure at 2.0MPa, react after 1 ~ 2 hour, venting is to normal pressure, continue reaction at being warming up to 310 ~ 320 DEG C after 1 ~ 2 hour simultaneously, constant temperature continues to vacuumize 0.3 ~ 1 hour, and reaction terminates, and supplements nitrogen when discharging.
Wherein in some embodiments, described polyesteramide is obtained by following synthetic method: the described monomer 2 after vacuum-drying joins in stirring-type polymerization reactor by (1), add simultaneously the titanium compound of 0.1 ~ 2% of described monomer 2 gross weight as catalyzer, add suitable quantity of water; Then vacuumize 3 ~ 10min, logical rare gas element 3 ~ 10min, so circulate 5 ~ 10 times, in the environment under making reactant be present in protection of inert gas, controlling system pressure in described stirring-type polymerization reactor is 0.1 ~ 0.5MPa;
(2) 240 ~ 260 DEG C are heated to by airtight for described stirring-type polymerization reactor, the stirring velocity of described stirring-type polymerization reactor is regulated to be 0 ~ 100r/min, wherein, when described stirring-type polyreaction actuator temperature reaches 210 DEG C, venting is to 1.6MPa, and maintain pressure at 1.6MPa, react after 0.5 ~ 4 hour, exit to normal pressure, reaction is continued after 0.5 ~ 4 hour at 240 ~ 260 DEG C, constant temperature continues to vacuumize 0.1 ~ 2 hour, and reaction terminates, the topping up when discharging;
In above-mentioned steps, described rare gas element is nitrogen or argon gas; Described titanium compound is one or more the mixture in tetrabutyl titanate, sec.-propyl titanic acid ester, propyl titanate, propenyl titanic acid ester.
Wherein in some embodiments, the organo montmorillonite of described molecular weight regulator to be add-on be 0.1 ~ 8% of described monomer 1 gross weight and add-on are the phenylformic acid of 0.1 ~ 3% of described monomer 1 gross weight; The N of described oxidation inhibitor to be add-on be 0.1 ~ 0.3% of monomer 1 gross weight, N`-bis-(2,2,6,6-tetramethyl--4-piperidyl)-1,3-benzene diamide.
Wherein in some embodiments, the add-on of described polyesteramide is 2 ~ 6% of described monomer 1 gross weight; The add-on of described organo montmorillonite is 0.5 ~ 5% of described monomer 1 gross weight, and described benzoic add-on is 0.5 ~ 2.5% of monomer 1 gross weight.
Principle of the present invention is as follows:
In order to solve the defect of polymeric amide 10T resin processing temperature narrow limits, invention has been the design of new resinous molecular structure, the fusing point of multipolymer is reduced by adding 11-aminoundecanoic acid, add polyesteramide to improve notched Izod impact strength and the antistatic effect of multipolymer simultaneously, add N, N`-bis-(2,2,6,6-tetramethyl--4-piperidyl)-1,3-benzene diamide processes xanthochromia problem in polymerization process.
Polyesteramide has ether oxygen base, and it can combine with free electric charge, and electric charge can move in the mode of combination, carries out ionic conduction release electrostatic lotus along polyesteramide backbone, thus reaches anlistatig effect.In addition, because the bond angle of ether-oxygen bond is comparatively large, segment kindliness is better, therefore can improve the notched Izod impact strength of multipolymer.
Organo montmorillonite belongs to poly-hydroxy inorganics, is reacted, reach the object of Molecular regulator amount by the terminal hydroxy group of organo montmorillonite and the end group of semiaromatic polyamide composition.In addition, because organo montmorillonite has nanometer small-size effect, it can improve modulus and the flame retardant resistance of multipolymer, reduces shrinking percentage and water-intake rate.
Phenylformic acid belongs to the organism of simple function group, and after in melt polymerization process, the Amino End Group of benzoic end carboxyl and semiaromatic polyamide composition reacts, it no longer carries out the reaction of chainpropagation, thus plays the effect of Molecular regulator amount.
N, N`-bis-(2,2,6,6-tetramethyl--4-piperidyl) fusing point of-1,3-benzene diamide is 272 DEG C, boiling point >360 DEG C, the better heat stability in semiaromatic polyamide composition building-up process, its amide group can react to improve consistency with the end group of semiaromatic polyamide composition, and hindered piperidine base can provide antioxygenation and improve the dyeability of multipolymer.
Compared with prior art, the present invention has following beneficial effect:
(1) the present invention is directed to the defect of existing polymeric amide 10T resin processing temperature narrow limits, carry out the design of new resinous molecular structure, the fusing point of multipolymer is reduced by adding 11-aminoundecanoic acid, add polyesteramide to improve notched Izod impact strength and the antistatic effect of multipolymer simultaneously, add N, N`-bis-(2, 2, 6, 6-tetramethyl--4-piperidyl)-1, 3-benzene diamide processes the xanthochromia problem in polymerization process, gained semiaromatic polyamide composition has higher mechanical property and resistance toheat, low water absorption, processing characteristics is excellent and have the characteristic of biogenetic derivation, can be applicable to field of electronics, LED field, automotive field, aerospace and military industry field etc.
(2) synthetic method of the present invention adopts the method for one-step polymerization, it has and decreases operation, shorten flow process, reduce cost, improve the advantage of productivity, preparation technology is easy, polymerization process is easy to operate, be convenient to management and control, required polymerizing condition can be reached fully, facilitate its industrialized realization; And do not use any organic solvent in the course of the polymerization process, to human body and environment not dangerous, security is good.
(3) decamethylene diamine used in the present invention, 11-aminoundecanoic acid are prepared by natural Viscotrol C and obtain, and therefore, it is a kind of bio-based materials that the present invention prepares semiaromatic polyamide composition, has the characteristic of environmental protection.
Accompanying drawing explanation
Figure 1 shows that the synthesis process flow diagram of semiaromatic polyamide composition of the present invention;
Figure 2 shows that the nonisothermal crystallization melting curve figure of the semiaromatic polyamide composition of the embodiment of the present invention 5 gained.
Embodiment
For understanding feature of the present invention, technique means and the specific purposes reached, function further, resolve the advantages and spirit of the present invention, by following examples, the present invention is further elaborated.
Semiaromatic polyamide composition of the present invention, it has as shown in the formula I structure:
In formula I, a=10 ~ 200, b=10 ~ 200, c=10 ~ 100, R is polyesteramide, and it has as shown in the formula II structure:
In formula II, x=10 ~ 200, y=10 ~ 200, z=10 ~ 100;
The reaction mechanism following (synthesis process flow diagram asks for an interview Fig. 1) of semiaromatic polyamide composition of the present invention:
From above-mentioned reaction formula, the Amino End Group of the Amino End Group of the Amino End Group of decamethylene diamine, the end carboxyl of terephthalic acid, 11-aminoundecanoic acid and end carboxyl, polyesteramide and end carboxyl, these groups can react to each other and obtain semiaromatic polyamide composition of the present invention.
And the reaction mechanism of the polyesteramide added in above-mentioned semiaromatic polyamide composition reaction process is as follows:
From above-mentioned reaction formula, the Amino End Group, 2 of its ester group, 11-aminoundecanoic acid after the open loop of 6-caprolactone, 2'-(1,3-phenylene) the oxazoline group of-bisoxazoline, these three kinds of groups can react to each other and obtain the polyesteramide that the present invention adds, the limiting viscosity of the polyesteramide that the present invention adds is 0.7 ~ 1.0dL/g, second-order transition temperature T
g>=80 DEG C, melt temperature T
mit is 215 ~ 225 DEG C.
The raw material that the embodiment of the present invention uses is as follows:
Decamethylene diamine, is selected from Wuxi Yinda Nylon Co., Ltd.;
Terephthalic acid, is selected from Beijing Yanshan Petrochemical Co.;
11-aminoundecanoic acid, is selected from Lian Zenong Chemical Co., Ltd. in Taiyuan;
Polyesteramide, self-control, the 6-caprolactone in raw material, is selected from Wuhan rich bamboo grove chemistry Science and Technology Ltd.;
2,2'-(1,3-phenylene)-bisoxazoline, is selected from colon, Nanjing medication chemistry company limited;
Tetrabutyl titanate, is selected from Chemical Reagent Co., Ltd., Sinopharm Group;
Organo montmorillonite, is selected from Zhejiang Fenghong New Material Co., Ltd.;
Phenylformic acid, is selected from Chemical Reagent Co., Ltd., Sinopharm Group;
N, N`-bis-(2,2,6,6-tetramethyl--4-piperidyl)-1,3-benzene diamide, is selected from Chemical Reagent Co., Ltd., Sinopharm Group.
The present invention is described in detail below in conjunction with specific embodiment.
Polyesteramide in following examples is by 11-aminoundecanoic acid, 6-caprolactone, 2,2'-(1,3-phenylene)-bisoxazoline copolymerization forms, 11-aminoundecanoic acid, 6-caprolactone, 2, the mol ratio of 2'-(1,3-phenylene)-bisoxazoline is 1:0.5 ~ 1:0.1 ~ 0.4.
Synthetic method is as follows:
(1) by monomer 2:11-aminoundecanoic acid, the 6-caprolactone, 2 after vacuum-drying, 2'-(1,3-phenylene)-bisoxazoline joins in stirring-type polymerization reactor by above-mentioned mol ratio, add simultaneously the titanium compound of 0.1 ~ 2% of monomer 2 gross weight as catalyzer, add the medium of appropriate water as mass-and heat-transfer; Then vacuumize 3 ~ 10min, logical rare gas element 3 ~ 10min, so circulates 5 ~ 10 times, and in the environment under making reactant be present in protection of inert gas, controlling system pressure in stirring-type polymerization reactor is 0.1 ~ 0.5MPa;
(2) 240 ~ 260 DEG C are heated to by airtight for stirring-type polymerization reactor, the stirring velocity regulating stirring-type polymerization reactor is 0 ~ 100r/min, wherein, when stirring-type polyreaction actuator temperature reaches 210 DEG C, venting is to 1.6MPa, and maintain pressure at 1.6MPa, react after 0.5 ~ 4 hour, exit to normal pressure, reaction is continued after 0.5 ~ 4 hour at 240 ~ 260 DEG C, constant temperature continues to vacuumize 0.1 ~ 2 hour, and reaction terminates, the topping up when discharging;
In above-mentioned steps, described rare gas element is nitrogen or argon gas; Described titanium compound is one or more the mixture in tetrabutyl titanate, sec.-propyl titanic acid ester, propyl titanate, propenyl titanic acid ester.
Embodiment 1
The raw material of the polyesteramide used in the present embodiment form and synthesis step as follows:
(1) by monomer 2:1006.6g (5mol) the 11-aminoundecanoic acid after vacuum-drying, 456.6g (4mol) 6-caprolactone, 270.3g (1.25mol) 2,2'-(1,3-phenylene)-bisoxazoline joins in stirring-type polymerization reactor, add simultaneously the tetrabutyl titanate (17.3g) of 1% of monomer 2 gross weight as catalyzer, add the medium of 500mL water as mass-and heat-transfer; Then vacuumize 5min, logical nitrogen 5min, so circulation 6 times, in the environment under making reactant be present in nitrogen protection, controlling system pressure in stirring-type polymerization reactor is 0.2MPa;
(2) in 2.5 hours by airtight for stirring-type polymerization reactor constant-speed heating to 250 DEG C, the stirring velocity regulating stirring-type polymerization reactor is 40r/min, wherein, when stirring-type polyreaction actuator temperature reaches 210 DEG C, venting is to 1.6MPa, and maintain pressure at 1.6MPa, react after 1.5 hours, exit to normal pressure, reaction is continued after 1.5 hours at 250 DEG C, constant temperature continues to vacuumize 0.5 hour, and reaction terminates, and supplements nitrogen when discharging.
The synthetic method of a kind of semiaromatic polyamide composition of the present embodiment, comprises the following steps:
(1) monomer 1:172.3g (1mol) decamethylene diamine after vacuum-drying, 166.1g (1mol) terephthalic acid, 10.1g (0.05mol) 11-aminoundecanoic acid are joined in stirring-type polymerization reactor, add the polyesteramide of 1% (3.5g) of monomer 1 gross weight, the organo montmorillonite of 0.1% (0.3g), the phenylformic acid of 0.1% (0.3g), the N of 0.1% (0.3g) simultaneously, N`-bis-(2,2,6,6-tetramethyl--4-piperidyl)-1,3-benzene diamide, add the medium of 100mL water as mass-and heat-transfer; Then vacuumize 5min, logical nitrogen 5min, so circulation 6 times, in the environment under making reactant be present in nitrogen protection, controlling system pressure in stirring-type polymerization reactor is 0.3MPa;
(2) in 4 hours by airtight for stirring-type polymerization reactor constant-speed heating to 285 DEG C, the stirring velocity regulating stirring-type polymerization reactor is 40r/min, wherein, when stirring-type polyreaction actuator temperature reaches 215 DEG C, venting is to 2.0MPa, and maintain pressure at 2.0MPa, react after 0.5 hour, exit to normal pressure, continue reaction at being warming up to 325 DEG C after 0.5 hour simultaneously, constant temperature continues to vacuumize 2 hours, and reaction terminates, and supplements nitrogen when discharging.
Embodiment 2
The raw material formation of polyesteramide used in the present embodiment and synthesis step are with embodiment 1.
The synthetic method of a kind of semiaromatic polyamide composition of the present embodiment, comprises the following steps:
(1) monomer 1:172.3g (1mol) decamethylene diamine after vacuum-drying, 166.1g (1mol) terephthalic acid, 40.3g (0.2mol) 11-aminoundecanoic acid are joined in stirring-type polymerization reactor, add polyesteramide, the organo montmorillonite of 8% (30.3g), the phenylformic acid of 3% (11.4g), the N of 0.3% (1.1g) of 8% (30.3g) of single 1 gross weight simultaneously, N`-bis-(2,2,6,6-tetramethyl--4-piperidyl)-1,3-benzene diamide, add the medium of 100mL water as mass-and heat-transfer; Then vacuumize 5min, logical nitrogen 5min, so circulation 6 times, in the environment under making stirring-type polymerization reactor be present in nitrogen protection, controlling system pressure in stirring-type polymerization reactor is 0.2MPa;
(2) in 2 hours by airtight for stirring-type polymerization reactor constant-speed heating to 270 DEG C, the stirring velocity regulating stirring-type polymerization reactor is 40r/min, wherein, when stirring-type polyreaction actuator temperature reaches 215 DEG C, venting is to 2.0MPa, and maintain pressure at 2.0MPa, react after 4 hours, exit to normal pressure, continue reaction at being warming up to 306 DEG C after 4 hours simultaneously, constant temperature continues to vacuumize 0.1 hour, and reaction terminates, and supplements nitrogen when discharging.
Embodiment 3
The raw material formation of polyesteramide used in the present embodiment and synthesis step are with embodiment 1.
The synthetic method of a kind of semiaromatic polyamide composition of the present embodiment, comprises the following steps:
(1) monomer 1:172.3g (1mol) decamethylene diamine after vacuum-drying, 166.1g (1mol) terephthalic acid, 20.1g (0.1mol) 11-aminoundecanoic acid are joined in stirring-type polymerization reactor, add polyesteramide, the organo montmorillonite of 0.5% (1.8g), the phenylformic acid of 0.5% (1.8g), the N of 0.2% (0.7g) of 2% (7.2g) of single 1 gross weight simultaneously, N`-bis-(2,2,6,6-tetramethyl--4-piperidyl)-1,3-benzene diamide, add the medium of 100mL water as mass-and heat-transfer; Then vacuumize 5min, logical nitrogen 5min, so circulation 6 times, in the environment under making reactant be present in nitrogen protection, controlling system pressure in stirring-type polymerization reactor is 0.3MPa;
(2) in 3.5 hours by airtight for stirring-type polymerization reactor constant-speed heating to 280 DEG C, the stirring velocity regulating stirring-type polymerization reactor is 40r/min, wherein, when stirring-type polyreaction actuator temperature reaches 215 DEG C, venting is to 2.0MPa, and maintain pressure at 2.0MPa, react after 1 hour, exit to normal pressure, continue reaction at being warming up to 320 DEG C after 1 hour simultaneously, constant temperature continues to vacuumize 1 hour, and reaction terminates, and supplements nitrogen when discharging.
Embodiment 4
The raw material formation of polyesteramide used in the present embodiment and synthesis step are with embodiment 1.
The synthetic method of a kind of semiaromatic polyamide composition of the present embodiment, comprises the following steps:
(1) monomer 1:172.3g (1mol) decamethylene diamine after vacuum-drying, 166.1g (1mol) terephthalic acid, 30.2g (0.15mol) 11-aminoundecanoic acid are joined in stirring-type polymerization reactor, add the polyesteramide of 6% (22.1g) of monomer 1 amount, the organo montmorillonite of 5% (18.4g), the phenylformic acid of 2.5% (9.2g), the N of 0.2% (0.7g) simultaneously, N`-bis-(2,2,6,6-tetramethyl--4-piperidyl)-1,3-benzene diamide, add the medium of 100mL water as mass-and heat-transfer; Then vacuumize 5min, logical nitrogen 5min, so circulation 6 times, in the environment under making reactant be present in nitrogen protection, controlling system pressure in stirring-type polymerization reactor is 0.3MPa;
(2) in 2.5 hours by airtight for stirring-type polymerization reactor constant-speed heating to 272 DEG C, the stirring velocity regulating stirring-type polymerization reactor is 40r/min, wherein, when stirring-type polymerization reactor reaches 215 DEG C, venting is to 2.0MPa, and maintain pressure at 2.0MPa, react after 2 hours, exit to normal pressure, continue reaction at being warming up to 310 DEG C after 2 hours simultaneously, constant temperature continues to vacuumize 0.3 hour, and reaction terminates, and supplements nitrogen when discharging.
Embodiment 5
The raw material formation of polyesteramide used in the present embodiment and synthesis step are with embodiment 1.
The synthetic method of a kind of semiaromatic polyamide composition of the present embodiment, comprises the following steps:
(1) monomer 1:172.3g (1mol) decamethylene diamine after vacuum-drying, 166.1g (1mol) terephthalic acid, 20.1g (0.1mol) 11-aminoundecanoic acid are joined in stirring-type polymerization reactor, add polyesteramide, the organo montmorillonite of 3% (10.8g), the phenylformic acid of 1.5% (5.4g), the N of 0.2% (0.7g) of 4% (14.3g) of single 1 gross weight simultaneously, N`-bis-(2,2,6,6-tetramethyl--4-piperidyl)-1,3-benzene diamide, add the medium of 100mL water as mass-and heat-transfer; Then vacuumize 5min, logical nitrogen 5min, so circulation 6 times, in the environment under making reactant be present in nitrogen protection, controlling system pressure in stirring-type polymerization reactor is 0.3MPa;
(2) in 3 hours by airtight for stirring-type polymerization reactor constant-speed heating to 275 DEG C, the stirring velocity regulating stirring-type polymerization reactor is 40r/min, wherein, when stirring-type polyreaction actuator temperature reaches 215 DEG C, venting is to 2.0MPa, and maintain pressure at 2.0MPa, react after 1.5 hours, exit to normal pressure, continue reaction at being warming up to 315 DEG C after 1.5 hours simultaneously, constant temperature continues to vacuumize 0.5 hour, and reaction terminates, and supplements nitrogen when discharging.
As shown in Figure 2, the melting peak-to-peak temperature (i.e. melt temperature) showing this semiaromatic polyamide composition in figure is 302.19 DEG C to the nonisothermal crystallization melting curve figure of the semiaromatic polyamide composition of the present embodiment gained.
Be below embodiment table look-up:
Table 1 embodiment raw material composition table look-up
Made for above-described embodiment sample is carried out following performance test:
Tensile property: by GB/T1040-2006 standard testing, rate of extension 50mm/min;
Impact property: by GB/T1843-2008 standard testing, batten thickness is 3.2mm;
Water-intake rate: by GB/T1034-2008 standard testing, thickness of test piece 2mm;
Limiting viscosity: by GB/T1632-2008 standard testing, the solvent vitriol oil;
Second-order transition temperature: by GB/T19466.2-2004 standard testing;
Melt temperature: by GB/T19466.3-2004 standard testing.
Table 2 embodiment performance table look-up
As can be seen from the above embodiments, the addition of 11-aminoundecanoic acid is more, and the tensile strength of semiaromatic polyamide composition, second-order transition temperature and melt temperature are lower, and shock strength is higher; The water-intake rate change of each embodiment is little; Along with the addition of molecular weight regulator (organo montmorillonite and phenylformic acid) increases, its limiting viscosity diminishes.Wherein, the over-all properties of embodiment 5 is best.
Each technical characteristic of the above embodiment can combine arbitrarily, for making description succinct, the all possible combination of each technical characteristic in above-described embodiment is not all described, but, as long as the combination of these technical characteristics does not exist contradiction, be all considered to be the scope that this specification sheets is recorded.
The above embodiment only have expressed several embodiment of the present invention, and it describes comparatively concrete and detailed, but can not therefore be construed as limiting the scope of the patent.It should be pointed out that for the person of ordinary skill of the art, without departing from the inventive concept of the premise, can also make some distortion and improvement, these all belong to protection scope of the present invention.Therefore, the protection domain of patent of the present invention should be as the criterion with claims.
Claims (10)
1. a semiaromatic polyamide composition, is characterized in that, it has as shown in the formula I structure:
In formula I, a=10 ~ 200, b=10 ~ 200, c=10 ~ 100, R is polyesteramide, and it has as shown in the formula II structure:
In formula II, x=10 ~ 200, y=10 ~ 200, z=10 ~ 100;
Described semiaromatic polyamide composition is formed by monomer 1 and polyesteramide copolymerization, described monomer 1 for mol ratio be decamethylene diamine, terephthalic acid, the 11-aminoundecanoic acid of 1:1:0.05 ~ 0.2, the add-on of described polyesteramide is 1 ~ 8% of described monomer 1 gross weight.
2. semiaromatic polyamide composition according to claim 1, is characterized in that, the add-on of described polyesteramide is 2 ~ 6% of described monomer 1 gross weight.
3. semiaromatic polyamide composition according to claim 1, is characterized in that, the limiting viscosity of described semiaromatic polyamide composition is 0.7 ~ 1.0dL/g, second-order transition temperature T
g>=100 DEG C, melt temperature T
mit is 295 ~ 305 DEG C.
4. semiaromatic polyamide composition according to claim 1, it is characterized in that, described polyesteramide is formed by monomer 2 copolymerization, described monomer 2 for mol ratio be 11-aminoundecanoic acid, the 6-caprolactone and 2 of 1:0.5 ~ 1:0.1 ~ 0.4,2'-(1,3-phenylene)-bisoxazoline.
5. semiaromatic polyamide composition according to claim 4, it is characterized in that, described polyesteramide is obtained by following synthetic method: the described monomer 2 after vacuum-drying joins in stirring-type polymerization reactor by (1), add simultaneously the titanium compound of 0.1 ~ 2% of described monomer 2 gross weight as catalyzer, add suitable quantity of water; Then vacuumize 3 ~ 10min, logical rare gas element 3 ~ 10min, so circulate 5 ~ 10 times, in the environment under making reactant be present in protection of inert gas, controlling system pressure in described stirring-type polymerization reactor is 0.1 ~ 0.5MPa;
(2) 240 ~ 260 DEG C are heated to by airtight for described stirring-type polymerization reactor, the stirring velocity of described stirring-type polymerization reactor is regulated to be 0 ~ 100r/min, wherein, when described stirring-type polyreaction actuator temperature reaches 210 DEG C, venting is to 1.6MPa, and maintain pressure at 1.6MPa, react after 0.5 ~ 4 hour, exit to normal pressure, reaction is continued after 0.5 ~ 4 hour at 240 ~ 260 DEG C, constant temperature continues to vacuumize 0.1 ~ 2 hour, and reaction terminates, the topping up when discharging;
In above-mentioned steps, described rare gas element is nitrogen or argon gas; Described titanium compound is one or more the mixture in tetrabutyl titanate, sec.-propyl titanic acid ester, propyl titanate, propenyl titanic acid ester.
6. a synthetic method for semiaromatic polyamide composition according to claim 1, is characterized in that, comprises the following steps:
(1) described monomer 1 is joined in stirring-type polymerization reactor, add described polyesteramide, molecular weight regulator, oxidation inhibitor, water simultaneously; Then vacuumize 3 ~ 10min, logical rare gas element 3 ~ 10min, so circulate 5 ~ 10 times, in the environment under making reactant be present in protection of inert gas, controlling system pressure in described stirring-type polymerization reactor is 0.1 ~ 0.5MPa; Described monomer 1 for mol ratio be decamethylene diamine, terephthalic acid, the 11-aminoundecanoic acid of 1:1:0.05 ~ 0.2, described polyesteramide add-on is add described monomer 1 gross weight 1 ~ 8%; Described polyesteramide is formed by monomer 2 copolymerization, described monomer 2 for mol ratio be 11-aminoundecanoic acid, 6-caprolactone, 2,2'-(1,3-phenylene)-bisoxazoline of 1:0.5 ~ 1:0.1 ~ 0.4;
(2) 270 ~ 285 DEG C are heated to by airtight for described stirring-type polymerization reactor, the stirring velocity of described stirring-type polymerization reactor is regulated to be 0 ~ 100r/min, wherein, when described stirring-type polyreaction actuator temperature reaches 215 DEG C, venting is to 2.0MPa, and maintain pressure at 2.0MPa, react after 0.5 ~ 4 hour, venting is to normal pressure, continue reaction at being warming up to 306 ~ 325 DEG C after 0.5 ~ 4 hour simultaneously, constant temperature continues to vacuumize 0.1 ~ 2 hour, and reaction terminates, the topping up when discharging;
In above-mentioned steps, described rare gas element is nitrogen or argon gas.
7. synthetic method according to claim 6, is characterized in that, comprises the following steps:
(1) the described monomer 1 after vacuum-drying is joined in stirring-type polymerization reactor, add described polyesteramide, molecular weight regulator, oxidation inhibitor, water simultaneously; Then vacuumize 4 ~ 6min, logical nitrogen 4 ~ 6min, so circulate 5 ~ 7 times, in the environment under making reactant be present in nitrogen protection, controlling system pressure in described stirring-type polymerization reactor is 0.2 ~ 0.3MPa;
(2) in 2 ~ 4 hours by described airtight constant-speed heating to 272 ~ 280 DEG C of stirring-type polymerization reactor, the stirring velocity of described stirring-type polymerization reactor is regulated to be 30 ~ 50r/min, wherein, when described stirring-type polyreaction actuator temperature reaches 215 DEG C, venting is to 2.0MPa, and maintain pressure at 2.0MPa, react after 1 ~ 2 hour, venting is to normal pressure, continue reaction at being warming up to 310 ~ 320 DEG C after 1 ~ 2 hour simultaneously, constant temperature continues to vacuumize 0.3 ~ 1 hour, and reaction terminates, and supplements nitrogen when discharging.
8. the synthetic method according to claim 6 or 7, it is characterized in that, described polyesteramide is obtained by following synthetic method: the described monomer 2 after vacuum-drying joins in stirring-type polymerization reactor by (1), add simultaneously the titanium compound of 0.1 ~ 2% of described monomer 2 gross weight as catalyzer, add suitable quantity of water; Then vacuumize 3 ~ 10min, logical rare gas element 3 ~ 10min, so circulate 5 ~ 10 times, in the environment under making reactant be present in protection of inert gas, controlling system pressure in described stirring-type polymerization reactor is 0.1 ~ 0.5MPa;
(2) 240 ~ 260 DEG C are heated to by airtight for described stirring-type polymerization reactor, the stirring velocity of described stirring-type polymerization reactor is regulated to be 0 ~ 100r/min, wherein, when described stirring-type polyreaction actuator temperature reaches 210 DEG C, venting is to 1.6MPa, and maintain pressure at 1.6MPa, react after 0.5 ~ 4 hour, exit to normal pressure, reaction is continued after 0.5 ~ 4 hour at 240 ~ 260 DEG C, constant temperature continues to vacuumize 0.1 ~ 2 hour, and reaction terminates, the topping up when discharging;
In above-mentioned steps, described rare gas element is nitrogen or argon gas; Described titanium compound is one or more the mixture in tetrabutyl titanate, sec.-propyl titanic acid ester, propyl titanate, propenyl titanic acid ester.
9. the synthetic method according to claim 6 or 7, is characterized in that, the organo montmorillonite of described molecular weight regulator to be add-on be 0.1 ~ 8% of described monomer 1 gross weight and add-on are the phenylformic acid of 0.1 ~ 3% of described monomer 1 gross weight; The N of described oxidation inhibitor to be add-on be 0.1 ~ 0.3% of monomer 1 gross weight, N`-bis-(2,2,6,6-tetramethyl--4-piperidyl)-1,3-benzene diamide.
10. synthetic method according to claim 9, is characterized in that, the add-on of described polyesteramide is 2 ~ 6% of described monomer 1 gross weight; The add-on of described organo montmorillonite is 0.5 ~ 5% of described monomer 1 gross weight, and described benzoic add-on is 0.5 ~ 2.5% of monomer 1 gross weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510890781.0A CN105348520B (en) | 2015-12-07 | 2015-12-07 | Semiaromatic polyamide composition and its synthetic method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510890781.0A CN105348520B (en) | 2015-12-07 | 2015-12-07 | Semiaromatic polyamide composition and its synthetic method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN105348520A true CN105348520A (en) | 2016-02-24 |
| CN105348520B CN105348520B (en) | 2017-09-19 |
Family
ID=55324594
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201510890781.0A Active CN105348520B (en) | 2015-12-07 | 2015-12-07 | Semiaromatic polyamide composition and its synthetic method |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN105348520B (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106675012A (en) * | 2016-12-05 | 2017-05-17 | 广东中塑新材料有限公司 | LDS polyamide composite material and preparation method thereof |
| CN107057341A (en) * | 2017-01-09 | 2017-08-18 | 广东中塑新材料有限公司 | High heat conductive insulating polyamide compoiste material and preparation method thereof |
| WO2022089674A1 (en) * | 2020-11-02 | 2022-05-05 | 上海凯赛生物技术股份有限公司 | Method for producing high temperature resistant polyamide, high temperature resistant polyamide and applications thereof |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4150002A (en) * | 1976-12-23 | 1979-04-17 | Schering Aktiengesellschaft | Polyamide melt adhesives |
| US4483975A (en) * | 1982-12-23 | 1984-11-20 | Plate Bonn Gesellschaft Mit Beschrankter Haftung | Copolyetheresteramides, process for their production and their use for the heat-sealing of textiles |
| US4644052A (en) * | 1985-08-15 | 1987-02-17 | Ashland Oil, Inc. | Reaction of bis-oxazoline with polycarboxylic acid catalyzed by alkali or alkaline earth metal cationic complex |
| CN1173190A (en) * | 1995-01-13 | 1998-02-11 | 巴斯福股份公司 | Biologically degradable polymers, processes for manufacturing the same and the use thereof for producing bioldegradable moulded articles |
| CN1837259A (en) * | 2005-03-21 | 2006-09-27 | 中国科学院成都有机化学有限公司 | Degradable polyester-amide copolymer and its preparation process |
| CN1849366A (en) * | 2003-08-08 | 2006-10-18 | 罗狄亚塑料工程股份有限公司 | Electrostatic composition based on a polyamide matrix |
-
2015
- 2015-12-07 CN CN201510890781.0A patent/CN105348520B/en active Active
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4150002A (en) * | 1976-12-23 | 1979-04-17 | Schering Aktiengesellschaft | Polyamide melt adhesives |
| US4483975A (en) * | 1982-12-23 | 1984-11-20 | Plate Bonn Gesellschaft Mit Beschrankter Haftung | Copolyetheresteramides, process for their production and their use for the heat-sealing of textiles |
| US4644052A (en) * | 1985-08-15 | 1987-02-17 | Ashland Oil, Inc. | Reaction of bis-oxazoline with polycarboxylic acid catalyzed by alkali or alkaline earth metal cationic complex |
| CN1173190A (en) * | 1995-01-13 | 1998-02-11 | 巴斯福股份公司 | Biologically degradable polymers, processes for manufacturing the same and the use thereof for producing bioldegradable moulded articles |
| CN1849366A (en) * | 2003-08-08 | 2006-10-18 | 罗狄亚塑料工程股份有限公司 | Electrostatic composition based on a polyamide matrix |
| CN1837259A (en) * | 2005-03-21 | 2006-09-27 | 中国科学院成都有机化学有限公司 | Degradable polyester-amide copolymer and its preparation process |
Non-Patent Citations (2)
| Title |
|---|
| ZHIYONG QIAN ET AL: "Synthesis and thermal degradation of biodegradable polyesteramide based on e-caprolactone and 11-aminoundecanoic acid", 《POLYMER DEGRADATION AND STABILITY》 * |
| 刘宇辰 等: "耐高温 PA10T /11 共聚尼龙的合成与表征", 《塑料工业》 * |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106675012A (en) * | 2016-12-05 | 2017-05-17 | 广东中塑新材料有限公司 | LDS polyamide composite material and preparation method thereof |
| CN106675012B (en) * | 2016-12-05 | 2019-02-12 | 广东中塑新材料有限公司 | Laser direct forming polyamide compoiste material and preparation method thereof |
| CN107057341A (en) * | 2017-01-09 | 2017-08-18 | 广东中塑新材料有限公司 | High heat conductive insulating polyamide compoiste material and preparation method thereof |
| CN107057341B (en) * | 2017-01-09 | 2019-07-19 | 广东中塑新材料有限公司 | High heat conductive insulating polyamide compoiste material and preparation method thereof |
| WO2022089674A1 (en) * | 2020-11-02 | 2022-05-05 | 上海凯赛生物技术股份有限公司 | Method for producing high temperature resistant polyamide, high temperature resistant polyamide and applications thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN105348520B (en) | 2017-09-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP6636947B2 (en) | Thermoplastic compositions made from polyamide polymers obtained from prepolymers and chain extenders and methods of manufacture | |
| CN105418918A (en) | High temperature resistant polyamide and synthesis method thereof | |
| KR20220055474A (en) | Polyamides and Corresponding Polymer Compositions, Articles and Methods of Making and Using | |
| CN105348520A (en) | Semi-aromatic polyamide and synthesis method thereof | |
| CN105295033A (en) | Long-carbon-chain semi-aromatic polyamide and synthetic method thereof | |
| CN105295031A (en) | High-temperature-resistant long-carbon-chain polyamide and synthesis method thereof | |
| CN105330846A (en) | Bio-based high-temperature-resistant polyamide and synthesis method thereof | |
| CN105348518A (en) | High-temperature resistant nylon and synthesis method thereof | |
| CN105295034A (en) | Biology-based semi-aromatic polyamide and synthesis method thereof | |
| CN105295032A (en) | Long-carbon-chain semi-aromatic nylon and synthetic method thereof | |
| CN105295035A (en) | One-step polymerized semi-aromatic polyesteramide and synthetic method thereof | |
| CN105330851A (en) | Long carbon chain transparent nylon and synthesizing method thereof | |
| CN105330844A (en) | Transparent nylon and synthetic method thereof | |
| CN108586734B (en) | Polyester-type polyamide 6 elastomer and its synthetic method | |
| CN105348515B (en) | Long carbon chain semi-aromatic transparent nylon and its synthetic method | |
| CN105330852B (en) | Long-carbon-chain transparent nylon and its synthetic method | |
| CN105482102A (en) | Semi-aromatic transparent polyamide and synthesis method thereof | |
| CN115286785B (en) | High-temperature-resistant nylon based on m-xylylenediamine and preparation method thereof | |
| CN105348517A (en) | Bio-based long carbon chain transparent polyamide and synthetic method thereof | |
| KR102118667B1 (en) | Preparation method of vegetable oil-derived polyamide 11 based thermoplastic polyamide elastomer alternating copolymer | |
| CN105348516A (en) | Long-carbon-chain semi-aromatic transparent polyamide and synthesis method thereof | |
| CN105330849A (en) | Long carbon chain transparent polyamide and synthesizing method thereof | |
| CN105330853A (en) | Bio-based transparent polyamide and synthesis method thereof | |
| CN105330845A (en) | Bio-based transparent nylon and synthesis method thereof | |
| CN105295036A (en) | Semi-aromatic polyesteramide and synthetic 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 | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant | ||
| TR01 | Transfer of patent right | ||
| TR01 | Transfer of patent right |
Effective date of registration: 20240110 Address after: Room 402, North Building, Kehui Building, No. 278 Changzhi Road, Taiyuan Xuefu Park, Taiyuan Comprehensive Reform Demonstration Zone, Shanxi Province, 030031 Patentee after: Taiyuan Zeyuan Technology Co.,Ltd. Address before: 030051 No. 3, Xueyuan Road, Shanxi, Taiyuan Patentee before: NORTH University OF CHINA |