CN1576314A - Polyacetal resin composition - Google Patents
Polyacetal resin composition Download PDFInfo
- Publication number
- CN1576314A CN1576314A CN 200410063506 CN200410063506A CN1576314A CN 1576314 A CN1576314 A CN 1576314A CN 200410063506 CN200410063506 CN 200410063506 CN 200410063506 A CN200410063506 A CN 200410063506A CN 1576314 A CN1576314 A CN 1576314A
- Authority
- CN
- China
- Prior art keywords
- polyacetal resin
- compound
- weight
- glass
- resin composite
- Prior art date
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- Granted
Links
- 229920006324 polyoxymethylene Polymers 0.000 title claims abstract description 108
- 229930182556 Polyacetal Natural products 0.000 title claims abstract description 106
- 239000011342 resin composition Substances 0.000 title claims abstract description 10
- 239000011347 resin Substances 0.000 claims abstract description 77
- 229920005989 resin Polymers 0.000 claims abstract description 77
- 239000011521 glass Substances 0.000 claims abstract description 42
- 150000001875 compounds Chemical class 0.000 claims description 33
- -1 cyclic ether compound Chemical class 0.000 claims description 27
- 239000000805 composite resin Substances 0.000 claims description 20
- 239000003365 glass fiber Substances 0.000 claims description 16
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 13
- 238000007334 copolymerization reaction Methods 0.000 claims description 13
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims description 13
- 229910000077 silane Inorganic materials 0.000 claims description 13
- 238000004132 cross linking Methods 0.000 claims description 10
- 125000004122 cyclic group Chemical group 0.000 claims description 9
- 238000002844 melting Methods 0.000 claims description 8
- 230000008018 melting Effects 0.000 claims description 8
- 150000004901 trioxanes Chemical class 0.000 claims description 4
- 229940059574 pentaerithrityl Drugs 0.000 claims description 3
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 3
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims 1
- 238000002156 mixing Methods 0.000 abstract description 2
- 239000011256 inorganic filler Substances 0.000 abstract 3
- 229910003475 inorganic filler Inorganic materials 0.000 abstract 3
- 239000000203 mixture Substances 0.000 description 25
- 238000011156 evaluation Methods 0.000 description 17
- 239000000463 material Substances 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 14
- 230000000704 physical effect Effects 0.000 description 12
- 238000004519 manufacturing process Methods 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 230000004927 fusion Effects 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 238000002347 injection Methods 0.000 description 5
- 239000007924 injection Substances 0.000 description 5
- 239000012756 surface treatment agent Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- NKDDWNXOKDWJAK-UHFFFAOYSA-N dimethoxymethane Chemical compound COCOC NKDDWNXOKDWJAK-UHFFFAOYSA-N 0.000 description 4
- HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical compound [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 229920005596 polymer binder Polymers 0.000 description 3
- 239000002491 polymer binding agent Substances 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 229930040373 Paraformaldehyde Natural products 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- 150000001642 boronic acid derivatives Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000009849 deactivation Effects 0.000 description 2
- 230000002708 enhancing effect Effects 0.000 description 2
- 150000002118 epoxides Chemical class 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 2
- 229920002521 macromolecule Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 150000004756 silanes Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- BYEAHWXPCBROCE-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropan-2-ol Chemical compound FC(F)(F)C(O)C(F)(F)F BYEAHWXPCBROCE-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- GNKIKWFLQLKHHD-UHFFFAOYSA-N CCCCC(CC)CO[Ti] Chemical compound CCCCC(CC)CO[Ti] GNKIKWFLQLKHHD-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920009382 Polyoxymethylene Homopolymer Polymers 0.000 description 1
- OUUQCZGPVNCOIJ-UHFFFAOYSA-M Superoxide Chemical compound [O-][O] OUUQCZGPVNCOIJ-UHFFFAOYSA-M 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229940008075 allyl sulfide Drugs 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 238000000071 blow moulding Methods 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- FPCJKVGGYOAWIZ-UHFFFAOYSA-N butan-1-ol;titanium Chemical compound [Ti].CCCCO.CCCCO.CCCCO.CCCCO FPCJKVGGYOAWIZ-UHFFFAOYSA-N 0.000 description 1
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 1
- HSAGRKXNQXYOCG-UHFFFAOYSA-N butane-1,4-diol dimethoxymethane Chemical compound COCOC.C(CCCO)O HSAGRKXNQXYOCG-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- PKTOVQRKCNPVKY-UHFFFAOYSA-N dimethoxy(methyl)silicon Chemical compound CO[Si](C)OC PKTOVQRKCNPVKY-UHFFFAOYSA-N 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 1
- SBRXLTRZCJVAPH-UHFFFAOYSA-N ethyl(trimethoxy)silane Chemical compound CC[Si](OC)(OC)OC SBRXLTRZCJVAPH-UHFFFAOYSA-N 0.000 description 1
- 229960005082 etohexadiol Drugs 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000009740 moulding (composite fabrication) Methods 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 125000005702 oxyalkylene group Chemical group 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000013034 phenoxy resin Substances 0.000 description 1
- 229920006287 phenoxy resin Polymers 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- AHJWSRRHTXRLAQ-UHFFFAOYSA-N tetramethoxymethane Chemical compound COC(OC)(OC)OC AHJWSRRHTXRLAQ-UHFFFAOYSA-N 0.000 description 1
- 238000001149 thermolysis Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- AQWKGXFXWCQPDB-UHFFFAOYSA-N trimethoxy(methoxymethoxy)methane Chemical compound COCOC(OC)(OC)OC AQWKGXFXWCQPDB-UHFFFAOYSA-N 0.000 description 1
- 238000007666 vacuum forming Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 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
- C08L59/00—Compositions of polyacetals; Compositions of derivatives of polyacetals
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
A polyacetal resin composition containing a glass inorganic filler is disclosed which has achieved excellent mechanical strength by improving adhesion between the glass inorganic filler and the polyacetal resin. The polyacetal resin composition is obtained by blending 100 parts by weight of a polyacetal resin component (A) with 3-200 parts by weight of a glass inorganic filler (B). As the polyacetal resin component (A), 99.9-80 parts by weight of a polyacetal resin (A1) substantially having a straight-chain molecular structure is used in combination with 0.1-20 parts by weight of a polyacetal resin (A2) having a branched or crosslinked structure.
Description
Technical field
The present invention relates to the polyacetal resin composite of mechanical characteristics excellence.
Background technology
In order to improve the mechanical characteristics of polyacetal resin, for example for intensity and rigidity, cooperating glass is that inorganic fillings etc. is known.
But, because polyacetal resin lacks activity and glass is that inorganic fillings also lacks activity, be glass that inorganic fillings is coupled in the polyacetal resin fusion and mixes simply, bond properties between the two is abundant inadequately, can not get the raising of desired mechanical characteristics in many cases.
For this reason, having proposed various is that the bond properties of inorganic fillings is to improve the method for mechanical characteristics about improving polyacetal resin and glass.
For example, in polyacetal resin, cooperate glass fibre and phenoxy resin (opening the claim scope of clear 49-98458 communique referring to the spy), adding glass fibre and superoxide and silane in polyacetal resin is coupler (opening the claim scope of clear 60-219252 communique referring to the spy), in polyoxymethylene (polyacetal resin), cooperate the glass fibre of (sizing) with the polyaminoester emulsion gluing, further make urethane contain silane coupling agent and (open the 1st～8 of the claim scope of clear 61-236851 communique referring to the spy, the 9th～13), in polyoxymethylene (polyacetal resin), cooperate and preferably carried out the surface-treated glass fibre and glass flake (is opened the claim scope the 1st of clear 62-91551 communique referring to the spy with silane coupling agent, 2), adding glass in polyacetal resin is inorganic fillings and boronic acid compounds, be that inorganic fillings carries out surface treatment and (opens the claim scope the 1st of flat 9-151298 communique referring to the spy to this glass further with particular silane compounds, the 4th), adding glass in polyacetal resin is inorganic fillings and hydroxy carboxylic acid compound, be that inorganic fillings carries out surface treatment and (opens the claim scope the 1st of 2002-371168 communique referring to the spy to this glass further with particular silane compounds, the 3rd) etc.
The content of invention
Yet any in these means all is to be the chemically active of inorganic fillings in order to improve glass, and only this also may not just can substantially improve and reach excellent physical strength with the bond properties of chemical inactive polyacetal resin.
The objective of the invention is to solve described problem, provide the field that utilizes that can adapt to enlarge the polyacetal resin composite of the requirement that higher mechanical characteristics is arranged that is proposed along with polyacetal resin in recent years.
The inventor etc., based on related problem, in order to obtain having the enhancing polyacetal resin composite of excellent mechanical rerum natura, carried out research painstakingly, the result finds, by cooperating polyacetal resin specified proportion, that introduced branching and crosslinking structure to be used as one of composition of polyacetal resin, just can significantly improve described problem, so far finished the present invention.
Promptly, the present invention is that to have cooperated the glass of 3～200 weight parts in 100 weight part polyacetal resin compositions (A) be the polyacetal resin composite of inorganic fillings (B), this polyacetal resin composite is characterised in that described polyacetal resin composition (A) is made of polyacetal resin polyacetal resin 99.9～80 weight parts, that be essentially straight-chain molecular structure (A1) and 0.1～20 weight part, that have branching or crosslinking structure (A2).
Summary of the invention
Describe the present invention below in detail.The invention is characterized in, having cooperated glass is in the enhancing polyacetal resin composite of inorganic fillings, and polyacetal resin composition (A) is by the polyacetal resin that is essentially straight-chain molecular structure (A1) and has branching or the polyacetal resin of crosslinking structure (A2) is constituted.
Used among the present invention have basically that the polyacetal resin of straight-chain molecular structure (A1) is with oxygen methylene radical (CH
2O-) no matter be the unitary macromolecular compound of primary structure, be any all right in polyoxymethylene homopolymer or the multipolymer (comprising segmented copolymer) that also contains a small amount of other structural unit except the oxygen methylene radical, especially serving as preferred with multipolymer.
Described multipolymer is meant mainly by oxygen methylene radical (CH
2O-) be dispersed with in the repeating unit of Gou Chenging carbonatoms 2～6 oxyalkylene constituted, weight-average molecular weight 5000 or above macromolecular compound.Generally, it be by the cyclic trimer Ji trioxane of formaldehyde be selected from compound copolymerization manufacturing in cyclic ether compound and the cyclic formal compound.Usually, after having removed terminal l fraction, be stable to thermolysis by hydrolysis.Described multipolymer serves as preferred with the resulting multipolymer of compound (b) copolymerization that is selected from cyclic ether compound and the cyclic formal compound by 99.9～90.0 weight % De trioxanes (a) and 0.1～10 weight %.In the occasion of using described multipolymer, effect of the present invention is just remarkable especially.
Cyclic ether compound or cyclic formal compound as copolymerization is used for example, can use oxyethane, 1,3-two oxa-s penta ring, glycol ether methylal, 1,4-butyleneglycol methylal etc.They are not form branching or crosslinking structure.
In addition, except mentioned component, general also the merging with the composition of regulating molecular weight uses, to regulate the molecular weight of resulting polymkeric substance.Example as the composition of regulating molecular weight is, do not form unstable terminal chain-transfer agent, that is, has in the compound of alkoxyl group a kind or more such as methylal, methoxy methyl acetal, dimethoxy methylal, trimethoxy methylal, oxygen methylene radical di-n-butyl ether and so on.
Above-mentioned and so on the polyacetal resin (A1) that uses among the present invention is that 1～50g/min person serves as preferred with the melting index of measuring under 190 ℃, 2160g load (MI).When MI was too small, poor processability excessively then was difficult to obtain effect of the present invention.
Secondly, the polyacetal resin with branching or crosslinking structure (A2) that uses among the present invention be by above-mentioned such make in the polyacetal resin (A1) further adding can with copolymerization such as formaldehyde Huo trioxane and by copolymerization can obtain forming branching or crosslink unit compound after copolymerization obtain.
As described polyacetal resin (A2), particularly preferably be and be selected from compound (b) in cyclic ether compound and the cyclic formal compound and the resulting multipolymer of polyfunctional glycidyl ether's compound (c) copolymerization of 0.01～1.0 weight % by 99.99～90.0 weight % De trioxanes (a) and 0-10 weight % with branching or crosslinking structure.
Here, in the manufacturing of above-mentioned branching or crosslined polyacetal resin (A2) employed trioxane (a), to be selected from compound (b) in cyclic ether compound and the cyclic formal compound be exactly the compound that is described in detail in the explanation as front polyacetal resin (A1).In the manufacturing of branching or crosslined polyacetal resin (A2) employed compound (b) and polyacetal resin (A1) in making used compound the same or different all right.Also have, the constituent that has the described polyacetal resin (A2) of branching or crosslinking structure for conduct, although described compound (b) is not necessary especially, but for the stable thermostability and the processibility of carrying out the manufacturing of branching crosslined polyacetal resin (A2) and improving resulting branching crosslined polyacetal resin (A2), with copolymerization 0.1～10 weight % serves as preferred, and 0.5～5 weight % is for preferred especially.
Be again, as polyfunctional glycidyl ether's compound (c), 3 or 4 glycidyl ether persons to be arranged in 1 molecule for preferred especially, specifically enumerated, be preferred compound with trihydroxymethylpropanyltri diglycidyl ether, T 55 and tetramethylolmethane four glycidyl ethers.The copolymerization ratio of described polyfunctional glycidyl ether's compound (c) is 0.01～1.0 weight %, with 0.02～0.5 weight % for preferred especially.
Branching used in the present invention or crosslined polyacetal resin (A2), the same with the polyacetal resin (A1) of front, generally to add an amount of molecular weight regulator, obtain by the methods such as cationoid polymerisation of using cationic polymerisation catalyst.Also have, catalyst deactivation processing after poly-unit, polymerizing condition, the polymerization and subsequent disposal etc. are all carried out also passable according to the manufacture method of polyacetal resin (A1).
The above-mentioned polyacetal resin (A2) that uses among the present invention is that 0.1～10g/min person serves as preferred with the melting index of measuring under 190 ℃, 2160g load (MI).When MI was too small, the processibility variation excessively then was difficult to obtain effect of the present invention.
In the present invention, constituting the polyacetal resin (A1) of polyacetal resin composition (A) and the weight ratio of branching or crosslined polyacetal (A2) is A1/A2=99.9～80 weight parts/0.1～20 weight part.Branching or crosslined polyacetal (A2) less than 0.1 weight part or when surpassing 20 weight parts, it is insufficient that the improvement of mechanical properties all becomes.Polyacetal resin (A1) is A1/A2=99.5～90 weight parts/0.5～10 weight part with the general preferred proportion of branching or crosslined polyacetal (A2).
Secondly, the glass that the present invention uses is that inorganic fillings (B) has been enumerated, the stopping composition of fibrous (glass fibre), granular (granulated glass sphere), powdery (milled glass fibre (ミ Le De ガ ラ ス Off ア イ バ one)), tabular (glass flake) and hollow form (glass sphere), particle diameter, staple length etc. to them have no particular limits, also the stopping composition that can use everybody all to know.
In the present invention, can be according to purpose and from these stopping composition, select a kind or more polyhybrid use.
In the present invention, be inorganic fillings though can use undressed these glass, but be that to have implemented the surface-treated inorganic fillings serve as preferred to surface treatment agent such as coupler to use with silane system or titanic acid ester.
As silane is coupler, enumerated, for example, vinyl alkoxy silane, oxirane TMOS, aminoalkoxy silane, sulfydryl organoalkoxysilane, alkoxy aryl silane etc.
As vinyl alkoxy silane, enumerated, for example, vinyltriethoxysilane, vinyltrimethoxy silane, vinyl three (beta-methoxy-oxyethyl group) silane etc.
As the oxirane TMOS, enumerated, for example, γ-glycidoxypropyltrime,hoxysilane, β-(3, the 4-epoxycyclohexyl) ethyl trimethoxy silane, γ-glycidoxy propyl-triethoxysilicane etc.
As aminoalkoxy silane, enumerated, for example, gamma-amino propyl trimethoxy silicane, γ-An Jibingjisanyiyangjiguiwan, gamma-amino propyl group methyl dimethoxysilane, gamma-amino propyl trimethoxy silicane, N-phenyl-gamma-amino propyl trimethoxy silicane etc.
As the sulfydryl organoalkoxysilane, enumerated, for example, γ-Qiu Jibingjisanjiayangjiguiwan, γ-sulfydryl propyl-triethoxysilicane etc.
As the allyl group organoalkoxysilane, enumerated, for example, γ-diallyl TSL 8330, γ-allyl amino propyl trimethoxy silicane, γ-allyl sulfide are for propyl trimethoxy silicane etc.
Wherein, serve as preferred the use with aminoalkoxy silane especially.
Also having, is surface treatment agent as titanic acid ester, enumerated, for example, the octylene ethyl glycolate titanium of isopropoxy, four titanium n-butoxide, four (2-ethyl hexyl oxy) titanium etc.
With respect to 100 weight part inorganic fillings, the consumption of surface treatment agent is 0.01～20 weight part, serves as preferred with 0.05～10 weight part, and 0.05～5 weight part is for preferred especially.
In addition, when glass was inorganic fillings (B) for glass fibre, further using polymer binder, adhesion promotor, other auxiliary agent etc. was suitable as cementing agent.As polymer binder, be generally organic materials, for example, material that water dispersible/water miscible polyvinyl acetate (PVA), polyester, epoxide, urethane, polyacrylic ester or polyolefin resin, their mixture etc. have always been known all is suitable use.
In the present invention, glass is that the use level of inorganic fillings (B) is 3～200 weight parts with respect to 100 weight part polyacetal resin compositions (A), preferred 5～150 weight parts, preferred especially 10～100 weight parts.During less than 3 weight parts, the improvement of mechanical properties is insufficient, and the processing that is shaped when surpassing 200 weight parts has become difficulty.
In the polyacetal resin composite of the present invention, can further cooperate known various stablizer, additive.As stablizer, that can enumerate has, hindered phenol based compound, melamine, 2, the oxyhydroxide of nitrogenous compounds such as 4-diamino-1,3,5-triazines, hydrazides, urea, alkali or alkaline-earth metal, inorganic salt, carboxylate salt etc. any a kind or more.Again, what the additive that uses among the present invention can be enumerated has, the general additive of thermoplastic resin, for example, tinting materials such as dyestuff, pigment, lubricant, nucleator, releasing agent, static inhibitor, tensio-active agent any a kind or more.
Have again,, except glass is inorganic fillings, can also cooperate fibrous, tabular, the powder shape stopping composition of a kind or how known inorganic, organic and metal etc. as long as in the scope that little amplitude descends as the performance of target molding of the present invention.The example of such stopping composition has been enumerated, and talcum, mica, wollastonite, carbon fiber etc. do not limit any in them.
In addition, in the polyacetal resin composite of the present invention, for example also can make up the interpolation of implementing special interpolation, the spy who opens the boronic acid compounds described in the flat 9-151298 communique and opening hydroxy carboxylic acid compound described in the 2002-371168 communique, the interpolation that also has always known organic acid and mineral acid etc., this might further improve mechanical properties.
Modulator approach for composition of the present invention has no particular limits, and is used in the modulation of resin combination always general used known device and method and just can modulates easily.For example, i) each composition is mixed after, the method for mixing, extruding and be modulated into the material grain and then be shaped with forcing machine; Ii) modulating part is formed different material grains, provides after this material grain predetermined amounts is mixed to be shaped and to obtain the method for the molding of target composition after being shaped; Iii) method in a kind in the composition or the how direct adding forming mill etc., any can use.Also have, preferably the part of resinous principle is made thin powder, mix with other composition again, add then, the method that makes the even cooperation of these compositions.
Also have, the resin combination relevant with the present invention also can be shaped by in extrusion molding, injection forming, compression molding, vacuum forming, blow molding, the foaming and molding any.
Embodiment
Specify the present invention with embodiment below, still, the present invention also not only is confined to these embodiment.Be that evaluation is carried out with following method again.
[melting index]
Melting index (MI) is measured under 190 ℃, load 2160g condition according to ASTM D-1238 standard.
[copolymerization composition]
With hexafluoroisopropanol d2 is solvent, by
1H NMR measures to determine its copolymerization composition.
＜tensile strength and stretching 〉
Tension test piece according to the ISO3167 standard is measured according to the ISO527 standard after 48 hours in placement under 23 ℃ of temperature, humidity 50% condition.
Production Example 1～3 (branching or crosslined polyacetal resin (A2))
Use is by the chuck that has the outside logical heat (cold) medium, the cross section is the machine barrel and the continous way hybrid reaction machine that rotating shaft constituted that has oar of the shape of overlapping of 2 circles, the rotating shaft of 2 band oars separately with the rotation of the rotating speed of 150rpm under, add trioxane (a) in ratio shown in the table 1, be selected from compound (b) and polyfunctional glycidyl ether's compound (c) in cyclic ether compound and the cyclic formal compound, further methylal as molecular weight regulator without interruption, and adding is the catalyzer boron trifluoride of 0.005 weight % with respect to trioxane continuously, carries out mass polymerization.The resultant of reaction of discharging from the polymerization machine adds 60 ℃ of aqueous solution of the triethylamine that contains 0.05 weight % simultaneously rapidly by crusher, makes catalyst deactivation.And then, separating, after the washing, drying, obtaining thick polyacetal resin.
Then, adding for these thick polyacetal resin 100 weight parts be the triethylamine of 3 weight % the 5 weight % aqueous solution, [3-(3 for the tetramethylolmethane four of 0.3 weight %, the 5-di-tert-butyl-hydroxy phenyl) propionic ester], in biaxial extruder, mix in 210 ℃ of fusions, remove l fraction, obtain the granular polyacetal resin of material, be used for the modulation of polyacetal resin composite.
Table 1 shows the composition and the melting index of these polyacetal resins.The implication of the abbreviation in the table is as follows:
Composition (b)
DO:1,3～two oxa-s, penta ring
BF:1,4-butyleneglycol methylal
Composition (c)
TMPTGE: trihydroxymethylpropanyltri diglycidyl ether
Table 1
| Branching crosslined polyacetal resin numbering | Trioxane (a) is % (wt) | Compound (b) | Compound (c) | Melting index MI g/10min | |||
| Kind | ???(wt)％ | Kind | ???(wt)％ | ||||
| Production Example 1 | ????A2-1 | ????98.2 | ????DO | ????1.7 | ?TMPTGE | ????0.1 | ????1.5 |
| Production Example 2 | ????A2-2 | ????98.2 | ????BF | ????1.7 | ?TMPTGE | ????0.1 | ????0.9 |
| Production Example 3 | ????A2-3 | ????98.0 | ????DO | ????1.7 | ?TMPTGE | ????0.3 | ????0.9 |
Embodiment 1～7, comparative example 1～3
(Polyplastic Co., Ltd. makes at the straight chain polyacetal resin, trade name: ジ ユ ラ コ Application M90), ((A2-1～A2-3) is with the forcing machine fusion of warm 200 ℃ of the tube combinations of modulation material grain that mixes for B1～B3) and branching crosslined polyacetal resin to cooperate various glass fibre shown below in ratio shown in the table 2.Then, with injection machine this combination material grain is configured as test piece, carries out evaluation of physical property with evaluation method shown in following, the result is illustrated in the table 2.
On the other hand, for relatively,, carry out evaluation of physical property to the situation that do not add branching crosslined polyacetal combinations of modulation material grain too.The result also is illustrated in the table 2 in the lump.
The unorganic glass of＜use is a stopping composition 〉
B1: carried out the surface-treated glass fibre with γ-An Jibingjisanyiyangjiguiwan
B2: carried out the surface-treated glass fibre with isopropoxy ethohexadiol acid esters titanium
B3: the glass fibre after further B1 being handled as polymer binder with epoxide
Table 2
| Resin is formed | The evaluation of physical property result | ||||||
| Polyacetal resin (A1) | Branching crosslined polyacetal resin (A2) | Glass is inorganic fillings (B) | Tensile strength | The tension elongation | |||
| Weight part | Kind | Weight part | Kind | Weight part | ????(MPa) | ??(％) | |
| Embodiment 1 | ????99 | ????A2-1 | ????1 | ????B1 | ????35 | ????121 | ????2.6 |
| Embodiment 2 | ????97 | ????A2-1 | ????3 | ????B1 | ????35 | ????138 | ????2.9 |
| Embodiment 3 | ????95 | ????A2-1 | ????5 | ????B1 | ????35 | ????141 | ????3.1 |
| Embodiment 4 | ????97 | ????A2-2 | ????3 | ????B1 | ????35 | ????132 | ????2.6 |
| Embodiment 5 | ????97 | ????A2-3 | ????3 | ????B1 | ????35 | ????130 | ????2.4 |
| Embodiment 6 | ????97 | ????A2-1 | ????3 | ????B2 | ????35 | ????128 | ????2.4 |
| Embodiment 7 | ????97 | ????A2-1 | ????3 | ????B3 | ????35 | ????139 | ????3.0 |
| Comparative example 1 | ????100 | ????- | ????- | ????B1 | ????35 | ????113 | ????1.9 |
| Comparative example 2 | ????100 | ????- | ????- | ????B2 | ????35 | ????110 | ????1.8 |
| Comparative example 3 | ????100 | ????- | ????- | ????B3 | ????35 | ????119 | ????2.0 |
Embodiment 8～15, comparative example 4～7
(Polyplastics Co., Ltd. makes at the straight chain polyacetal resin, trade name: ジ ユ ラ コ Application M90), ((A2-1～A2-3) is with the forcing machine fusion of warm 200 ℃ of the tube combinations of modulation material grain that mixes for B4～B7) and branching crosslined polyacetal resin to cooperate various granulated glass sphere shown below in ratio shown in the table 3.Then, with injection machine this combination material grain is configured as test piece, carries out evaluation of physical property with evaluation method shown in following, the result is illustrated in the table 3.
On the other hand, for relatively,, carry out evaluation of physical property to the situation modulation group compound granulation too that does not add branching, crosslined polyacetal.The result also is illustrated in the table 3 in the lump.
The inorganic fillings of＜use 〉
B4: the granulated glass sphere that does not use surface treatment agent
B5: carried out the surface-treated granulated glass sphere with γ-An Jibingjisanyiyangjiguiwan
B6: carried out the surface-treated granulated glass sphere with vinyltriethoxysilane
B7: carried out the surface-treated granulated glass sphere with γ-glycidoxy propyl-triethoxysilicane
Table 3
| Resin is formed | The evaluation of physical property result | ||||||
| Polyacetal resin (A1) | Branching crosslined polyacetal resin (A2) | Glass is inorganic fillings (B) | Tensile strength | The tension elongation | |||
| Weight part | Kind | Weight part | Kind | Weight part | ??(MPa) | ??(％) | |
| Embodiment 8 | ????97 | ????A2-1 | ????3 | ????B4 | ????35 | ????57 | ????16 |
| Embodiment 9 | ????99 | ????A2-1 | ????1 | ????B5 | ????35 | ????53 | ????15 |
| Embodiment 10 | ????97 | ????A2-1 | ????3 | ????B5 | ????35 | ????62 | ????18 |
| Embodiment 11 | ????95 | ????A2-1 | ????5 | ????B5 | ????35 | ????64 | ????19 |
| Embodiment 12 | ????97 | ????A2-2 | ????3 | ????B5 | ????35 | ????59 | ????16 |
| Embodiment 13 | ????97 | ????A2-3 | ????3 | ????B5 | ????35 | ????60 | ????17 |
| Embodiment 14 | ????97 | ????A2-1 | ????3 | ????B6 | ????35 | ????60 | ????17 |
| Embodiment 15 | ????97 | ????A2-1 | ????3 | ????B7 | ????35 | ????59 | ????17 |
| Comparative example 4 | ????100 | ????- | ????- | ????B4 | ????35 | ????45 | ????11 |
| Comparative example 5 | ????100 | ????- | ????- | ????B5 | ????35 | ????47 | ????12 |
| Comparative example 6 | ????100 | ????- | ????- | ????B6 | ????35 | ????48 | ????13 |
| Comparative example 7 | ????100 | ????- | ????- | ????B7 | ????35 | ????48 | ????13 |
Embodiment 16～21, comparative example 8～9
(Polyplastics Co., Ltd. makes at the straight chain polyacetal resin, trade name: ジ ユ ラ コ Application M270), cooperate various milled glass fibre shown below (B8, B9) and branching crosslined polyacetal resin in ratio shown in the table 4, with the forcing machine fusion of warm 200 ℃ of the tube combinations of modulation material grain that mixes.Then, with injection machine this combination material grain is configured as test piece, carries out evaluation of physical property with evaluation method shown in following, the result is illustrated in the table 4.
On the other hand, for relatively,, carry out evaluation of physical property to the situation that do not add branching crosslined polyacetal combinations of modulation material grain too.The result also is illustrated in the table 4 in the lump.
The unorganic glass of＜use is a stopping composition 〉
B8: the glass fibre that does not use surface treatment agent
B9: carried out the surface-treated milled glass fibre with γ-An Jibingjisanyiyangjiguiwan
Table 4
| Resin is formed | The evaluation of physical property result | ||||||
| Polyacetal resin (A1) | Branching crosslined polyacetal resin (A2) | Glass is inorganic fillings (B) | Tensile strength | The tension elongation | |||
| Weight part | Kind | Weight part | Kind | Weight part | ??(MPa) | ??(％) | |
| Embodiment 16 | ????99 | ????A2-1 | ????1 | ????B8 | ????30 | ????54 | ????13 |
| Embodiment 17 | ????97 | ????A2-1 | ????3 | ????B8 | ????30 | ????58 | ????15 |
| Embodiment 18 | ????95 | ????A2-1 | ????5 | ????B8 | ????30 | ????60 | ????16 |
| Embodiment 19 | ????97 | ????A2-2 | ????3 | ????B8 | ????30 | ????57 | ????15 |
| Embodiment 20 | ????97 | ????A2-3 | ????3 | ????B8 | ????30 | ????60 | ????16 |
| Embodiment 21 | ????97 | ????A2-1 | ????3 | ????B9 | ????30 | ????63 | ????18 |
| Comparative example 8 | ????100 | ????- | ????- | ????B8 | ????30 | ????45 | ????11 |
| Comparative example 9 | ????100 | ????- | ????- | ????B9 | ????30 | ????47 | ????12 |
Embodiment 22～26, comparative example 10
(Polyplastics Co., Ltd. makes at the straight chain polyacetal resin, trade name: ジ ユ ラ コ Application M90), (A2-1～A2-3) is with the forcing machine fusion of 200 ℃ of the tube temperature combinations of modulation material grain that mixes to cooperate various glass flake shown below and branching crosslined polyacetal resin in ratio shown in the table 5.Then, with injection machine this combination material grain is configured as test piece, carries out evaluation of physical property with evaluation method shown in following, the result is illustrated in the table 5.
On the other hand, for relatively,, carry out evaluation of physical property to the situation that do not add branching crosslined polyacetal combinations of modulation material grain too.The result also is illustrated in the table 5 in the lump.
The unorganic glass of＜use is a stopping composition 〉
B10: carried out the surface-treated glass flake with γ-An Jibingjisanyiyangjiguiwan
Table 5
| Resin is formed | The evaluation of physical property result | ||||||
| Polyacetal resin (A1) | Branching crosslined polyacetal resin (A2) | Glass is inorganic fillings (B) | Tensile strength | The tension elongation | |||
| Weight part | Kind | Weight part | Kind | Weight part | ???(MPa) | ????(％) | |
| Embodiment 22 | ????99 | ????A2-1 | ????1 | ????B10 | ????35 | ????66 | ????4.3 |
| Embodiment 23 | ????97 | ????A2-1 | ????3 | ????B10 | ????35 | ????70 | ????4.6 |
| Embodiment 24 | ????95 | ????A2-1 | ????5 | ????B10 | ????35 | ????72 | ????4.8 |
| Embodiment 25 | ????97 | ????A2-2 | ????3 | ????B10 | ????35 | ????69 | ????4.4 |
| Embodiment 26 | ????97 | ????A2-3 | ????3 | ????B10 | ????35 | ????69 | ????4.5 |
| Comparative example 10 | ????100 | ????- | ????- | ????B10 | ????35 | ????59 | ????3.7 |
Claims (9)
1. polyacetal resin composite, it is characterized in that it is is the formed polyacetal resin composite of inorganic fillings (B) by the glass that has cooperated 3～200 weight parts in 100 weight part polyacetal resin compositions (A), described polyacetal resin composition (A) is the polyacetal resin (A1) that is essentially straight-chain molecular structure by having of 99.9～80 weight parts and the polyacetal resin with branching or crosslinking structure (A2) of 0.1～20 weight part is constituted.
2. the polyacetal resin composite described in the claim 1, its described polyacetal resin (A1) are by be selected from the multipolymer that compound (b) copolymerization in cyclic ether compound and cyclic formal compound obtain of 99.9～90.0 weight % De trioxanes (a) with 0.1～10 weight %.
3. the polyacetal resin composite described in the claim 1, its described polyacetal resin (A2) with branching or crosslinking structure are the multipolymers that polyfunctional glycidyl ether's compound (c) copolymerization that is selected from compound (b) in cyclic ether compound and the cyclic formal compound and 0.01～1.0 weight % by 99.99～90.0 weight % De trioxanes (a) and 0～10 weight % obtains.
4. the polyacetal resin composite described in the claim 3, its described polyfunctional glycidyl ether's compound (c) has 3 or 4 glycidyls.
5. the polyacetal resin composite described in the claim 3, its described polyfunctional glycidyl ether's compound (c) is selected from trihydroxymethylpropanyltri diglycidyl ether, T 55 and tetramethylolmethane four glycidyl ethers.
6. any 1 described polyacetal resin composite in the claim 1～5, its described polyacetal resin (A1) is that melting index is the resin of 1～50g/min, and described polyacetal resin (A2) with branching or crosslinking structure is that melting index is the resin of 0.1～10g/min.
7. any 1 described polyacetal resin composite in the claim 1～5, its described glass is that inorganic fillings (B) is at least a kind that is selected from glass fibre, granulated glass sphere, milled glass fibre and the glass flake.
8. the polyacetal resin composite described in the claim 1, its described glass are that inorganic fillings (B) is to be that coupler has carried out surface-treated with silane.
9. the polyacetal resin composite described in the claim 8, its described silane is that coupler is an aminoalkoxy silane.
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| JP271825/2003 | 2003-07-08 | ||
| JP271825/03 | 2003-07-08 | ||
| JP2003271825A JP2005029714A (en) | 2003-07-08 | 2003-07-08 | Polyacetal resin composition |
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| CN1331940C CN1331940C (en) | 2007-08-15 |
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|---|---|---|---|---|
| CN102264833B (en) * | 2008-12-24 | 2013-07-17 | 宝理塑料株式会社 | Polyacetal resin composition |
| CN108699318A (en) * | 2016-03-31 | 2018-10-23 | 宝理塑料株式会社 | Polyacetal resin composite |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2008044995A (en) * | 2006-08-11 | 2008-02-28 | Polyplastics Co | Polyacetal resin composition |
| JP2008156505A (en) * | 2006-12-25 | 2008-07-10 | Polyplastics Co | Polyacetal resin composition |
| USD782859S1 (en) | 2016-02-12 | 2017-04-04 | Haworth, Inc. | Back support for a chair |
| USD793787S1 (en) | 2016-02-12 | 2017-08-08 | Haworth, Inc. | Portion of a back support for a chair |
| USD779248S1 (en) | 2016-02-12 | 2017-02-21 | Haworth, Inc. | Armrests for a chair |
| USD779253S1 (en) | 2016-02-12 | 2017-02-21 | Haworth, Inc. | Back support for a chair |
| USD779251S1 (en) | 2016-02-12 | 2017-02-21 | Haworth, Inc. | Lumbar support for a chair |
| USD782241S1 (en) | 2016-02-12 | 2017-03-28 | Haworth, Inc. | Back support for a chair |
| USD779252S1 (en) | 2016-02-12 | 2017-02-21 | Haworth, Inc. | Back support for a chair |
| USD779255S1 (en) | 2016-02-12 | 2017-02-21 | Haworth, Inc. | Headrest for a chair |
| USD779250S1 (en) | 2016-02-12 | 2017-02-21 | Haworth, Inc. | Portion of a back support for a chair |
| USD779254S1 (en) | 2016-02-12 | 2017-02-21 | Haworth, Inc. | Armrests for a chair |
| USD784749S1 (en) | 2016-02-12 | 2017-04-25 | Haworth, Inc. | Lumbar support for a chair |
| JP7339812B2 (en) * | 2019-08-30 | 2023-09-06 | ポリプラスチックス株式会社 | Polyacetal resin composition and method for producing the same |
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| JPS60219252A (en) * | 1984-04-13 | 1985-11-01 | Nitto Boseki Co Ltd | Glass fiber reinforced polyacetal resin composition |
| JP3285480B2 (en) * | 1995-09-29 | 2002-05-27 | ポリプラスチックス株式会社 | Polyacetal resin composition |
| JP3083474B2 (en) * | 1996-03-05 | 2000-09-04 | ポリプラスチックス株式会社 | Polyacetal resin composition and molded article |
| JP4762387B2 (en) * | 1999-06-23 | 2011-08-31 | ポリプラスチックス株式会社 | Polyacetal resin composition |
| DE10082535B4 (en) * | 1999-07-30 | 2007-04-05 | Asahi Kasei Kabushiki Kaisha | Use of polyacetal block copolymers |
| JP2001089631A (en) * | 1999-09-24 | 2001-04-03 | Polyplastics Co | Branched polyacetal resin composition |
| JP4889157B2 (en) * | 2001-04-05 | 2012-03-07 | 旭化成ケミカルズ株式会社 | Polyoxymethylene resin composition |
| JP4979857B2 (en) * | 2001-06-15 | 2012-07-18 | ポリプラスチックス株式会社 | Polyacetal resin composition |
| JP3584930B2 (en) * | 2002-02-19 | 2004-11-04 | セイコーエプソン株式会社 | Semiconductor device and manufacturing method thereof, circuit board, and electronic apparatus |
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| CN102264833B (en) * | 2008-12-24 | 2013-07-17 | 宝理塑料株式会社 | Polyacetal resin composition |
| CN108699318A (en) * | 2016-03-31 | 2018-10-23 | 宝理塑料株式会社 | Polyacetal resin composite |
| CN108699318B (en) * | 2016-03-31 | 2021-04-30 | 宝理塑料株式会社 | Polyacetal resin composition |
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| CN1331940C (en) | 2007-08-15 |
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