JP2006193704A - 樹脂組成物用帯電防止剤 - Google Patents
樹脂組成物用帯電防止剤 Download PDFInfo
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- JP2006193704A JP2006193704A JP2005078438A JP2005078438A JP2006193704A JP 2006193704 A JP2006193704 A JP 2006193704A JP 2005078438 A JP2005078438 A JP 2005078438A JP 2005078438 A JP2005078438 A JP 2005078438A JP 2006193704 A JP2006193704 A JP 2006193704A
- Authority
- JP
- Japan
- Prior art keywords
- imidate
- bis
- trifluoromethanesulfonyl
- resin composition
- antistatic agent
- 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
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- 239000011342 resin composition Substances 0.000 title claims abstract description 46
- 239000002216 antistatic agent Substances 0.000 title claims abstract description 32
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 79
- 150000003839 salts Chemical class 0.000 claims abstract description 22
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 6
- 125000003118 aryl group Chemical group 0.000 claims abstract description 5
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 5
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 4
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 4
- 239000000853 adhesive Substances 0.000 claims description 9
- 230000001070 adhesive effect Effects 0.000 claims description 9
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 7
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 125000004437 phosphorous atom Chemical group 0.000 claims description 4
- 125000004429 atom Chemical group 0.000 claims description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 3
- 125000004434 sulfur atom Chemical group 0.000 claims description 3
- 239000000126 substance Substances 0.000 abstract description 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- CEIPQQODRKXDSB-UHFFFAOYSA-N ethyl 3-(6-hydroxynaphthalen-2-yl)-1H-indazole-5-carboximidate dihydrochloride Chemical compound Cl.Cl.C1=C(O)C=CC2=CC(C3=NNC4=CC=C(C=C43)C(=N)OCC)=CC=C21 CEIPQQODRKXDSB-UHFFFAOYSA-N 0.000 description 127
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 description 120
- -1 halogen ion Chemical class 0.000 description 17
- 229920000647 polyepoxide Polymers 0.000 description 15
- 229920005989 resin Polymers 0.000 description 15
- 239000011347 resin Substances 0.000 description 15
- 239000003822 epoxy resin Substances 0.000 description 14
- 239000011248 coating agent Substances 0.000 description 12
- 238000000576 coating method Methods 0.000 description 12
- 239000000976 ink Substances 0.000 description 12
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 10
- 238000011156 evaluation Methods 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 8
- 230000001133 acceleration Effects 0.000 description 7
- 150000002009 diols Chemical class 0.000 description 7
- 239000000178 monomer Substances 0.000 description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 5
- 229920000178 Acrylic resin Polymers 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- 150000001768 cations Chemical class 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000007613 environmental effect Effects 0.000 description 4
- ZUZLIXGTXQBUDC-UHFFFAOYSA-N methyltrioctylammonium Chemical compound CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC ZUZLIXGTXQBUDC-UHFFFAOYSA-N 0.000 description 4
- 229920001778 nylon Polymers 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- VPEYTQLEAVUCQV-UHFFFAOYSA-N O=S(C(F)(F)F)(C1=CNC(S(C(F)(F)F)(=O)=O)=N1)=O Chemical group O=S(C(F)(F)F)(C1=CNC(S(C(F)(F)F)(=O)=O)=N1)=O VPEYTQLEAVUCQV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 3
- 239000002563 ionic surfactant Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229920005672 polyolefin resin Polymers 0.000 description 3
- 229920005749 polyurethane resin Polymers 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical group CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 125000002883 imidazolyl group Chemical group 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 229920003986 novolac Polymers 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- UGUHFDPGDQDVGX-UHFFFAOYSA-N 1,2,3-thiadiazole Chemical group C1=CSN=N1 UGUHFDPGDQDVGX-UHFFFAOYSA-N 0.000 description 1
- ONIRYHNNJGLNRI-UHFFFAOYSA-N 1-[2-(2-methoxyethoxy)ethyl]-1-methylpiperidin-1-ium Chemical compound COCCOCC[N+]1(C)CCCCC1 ONIRYHNNJGLNRI-UHFFFAOYSA-N 0.000 description 1
- XONISLBETRQNCL-UHFFFAOYSA-N 1-[2-(2-methoxyethoxy)ethyl]-1-methylpyrrolidin-1-ium Chemical compound COCCOCC[N+]1(C)CCCC1 XONISLBETRQNCL-UHFFFAOYSA-N 0.000 description 1
- UVCPHBWNKAXVPC-UHFFFAOYSA-N 1-butyl-1-methylpiperidin-1-ium Chemical compound CCCC[N+]1(C)CCCCC1 UVCPHBWNKAXVPC-UHFFFAOYSA-N 0.000 description 1
- PXELHGDYRQLRQO-UHFFFAOYSA-N 1-butyl-1-methylpyrrolidin-1-ium Chemical compound CCCC[N+]1(C)CCCC1 PXELHGDYRQLRQO-UHFFFAOYSA-N 0.000 description 1
- BHIGPVGNEXDQBL-UHFFFAOYSA-N 1-butyl-2-methylpyridin-1-ium Chemical compound CCCC[N+]1=CC=CC=C1C BHIGPVGNEXDQBL-UHFFFAOYSA-N 0.000 description 1
- IQQRAVYLUAZUGX-UHFFFAOYSA-N 1-butyl-3-methylimidazolium Chemical compound CCCCN1C=C[N+](C)=C1 IQQRAVYLUAZUGX-UHFFFAOYSA-N 0.000 description 1
- DADKKHHMGSWSPH-UHFFFAOYSA-N 1-butyl-3-methylpyridin-1-ium Chemical compound CCCC[N+]1=CC=CC(C)=C1 DADKKHHMGSWSPH-UHFFFAOYSA-N 0.000 description 1
- NNLHWTTWXYBJBQ-UHFFFAOYSA-N 1-butyl-4-methylpyridin-1-ium Chemical compound CCCC[N+]1=CC=C(C)C=C1 NNLHWTTWXYBJBQ-UHFFFAOYSA-N 0.000 description 1
- ITMKMGFAZDZEPE-UHFFFAOYSA-N 1-decyl-1-methylpiperidin-1-ium Chemical compound CCCCCCCCCC[N+]1(C)CCCCC1 ITMKMGFAZDZEPE-UHFFFAOYSA-N 0.000 description 1
- YPKUOQRBNZPMAE-UHFFFAOYSA-N 1-decyl-1-methylpyrrolidin-1-ium Chemical compound CCCCCCCCCC[N+]1(C)CCCC1 YPKUOQRBNZPMAE-UHFFFAOYSA-N 0.000 description 1
- UVNUAVZGUKYSDI-UHFFFAOYSA-N 1-decyl-2-methylpyridin-1-ium Chemical compound CCCCCCCCCC[N+]1=CC=CC=C1C UVNUAVZGUKYSDI-UHFFFAOYSA-N 0.000 description 1
- LDVVBLGHGCHZBJ-UHFFFAOYSA-N 1-decyl-3-methylimidazolium Chemical compound CCCCCCCCCCN1C=C[N+](C)=C1 LDVVBLGHGCHZBJ-UHFFFAOYSA-N 0.000 description 1
- MFMBELVKZWEQOM-UHFFFAOYSA-N 1-decylpyridin-1-ium Chemical compound CCCCCCCCCC[N+]1=CC=CC=C1 MFMBELVKZWEQOM-UHFFFAOYSA-N 0.000 description 1
- NJMWOUFKYKNWDW-UHFFFAOYSA-N 1-ethyl-3-methylimidazolium Chemical compound CCN1C=C[N+](C)=C1 NJMWOUFKYKNWDW-UHFFFAOYSA-N 0.000 description 1
- IXSSETPVBLTFMF-UHFFFAOYSA-N 1-heptyl-1-methylpiperidin-1-ium Chemical compound CCCCCCC[N+]1(C)CCCCC1 IXSSETPVBLTFMF-UHFFFAOYSA-N 0.000 description 1
- XZDPRAGZNFQVIM-UHFFFAOYSA-N 1-heptyl-1-methylpyrrolidin-1-ium Chemical compound CCCCCCC[N+]1(C)CCCC1 XZDPRAGZNFQVIM-UHFFFAOYSA-N 0.000 description 1
- YMDCKNLPLNSVMT-UHFFFAOYSA-N 1-heptyl-2-methylpyridin-1-ium Chemical compound CCCCCCC[N+]1=CC=CC=C1C YMDCKNLPLNSVMT-UHFFFAOYSA-N 0.000 description 1
- FCZZZYZIQDHCIW-UHFFFAOYSA-N 1-heptyl-3-methylimidazol-3-ium Chemical compound CCCCCCC[N+]=1C=CN(C)C=1 FCZZZYZIQDHCIW-UHFFFAOYSA-N 0.000 description 1
- RINDUOTXMPEVDX-UHFFFAOYSA-N 1-heptyl-3-methylpyridin-1-ium Chemical compound CCCCCCC[N+]1=CC=CC(C)=C1 RINDUOTXMPEVDX-UHFFFAOYSA-N 0.000 description 1
- IKTJZDYHCSGZBL-UHFFFAOYSA-N 1-heptyl-4-methylpyridin-1-ium Chemical compound CCCCCCC[N+]1=CC=C(C)C=C1 IKTJZDYHCSGZBL-UHFFFAOYSA-N 0.000 description 1
- BOFYFGANDNPXEM-UHFFFAOYSA-N 1-heptylpyridin-1-ium Chemical compound CCCCCCC[N+]1=CC=CC=C1 BOFYFGANDNPXEM-UHFFFAOYSA-N 0.000 description 1
- FHZKIKVDRZVWKN-UHFFFAOYSA-N 1-hexyl-1-methylpiperidin-1-ium Chemical compound CCCCCC[N+]1(C)CCCCC1 FHZKIKVDRZVWKN-UHFFFAOYSA-N 0.000 description 1
- SVONMDAUOJGXHL-UHFFFAOYSA-N 1-hexyl-1-methylpyrrolidin-1-ium Chemical compound CCCCCC[N+]1(C)CCCC1 SVONMDAUOJGXHL-UHFFFAOYSA-N 0.000 description 1
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NJICVKXEONIFAZ-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethyl-trimethylazanium Chemical compound COCCOCC[N+](C)(C)C NJICVKXEONIFAZ-UHFFFAOYSA-N 0.000 description 1
- AIPWFQFPGUZDNB-UHFFFAOYSA-N 2-methyl-1-nonylpyridin-1-ium Chemical compound CCCCCCCCC[N+]1=CC=CC=C1C AIPWFQFPGUZDNB-UHFFFAOYSA-N 0.000 description 1
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- 239000004593 Epoxy Substances 0.000 description 1
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- Inks, Pencil-Leads, Or Crayons (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
【解決手段】 式(1):
(R1R2R3R4Y)+・(CF3SO2)2N− (1)[式中、R1、R2、R3及びR4は、アルキル基又は式(2):R5OCH2CH2OCH2CH2− (2)(式中、R5はメチル基又はエチル基を示す。)で表されるアルキルオキシエトキシエチル基を示し、R1、R2、R3及びR4のいずれか二つが末端で互いに結合してアルキレン鎖を形成していてもよい。Yは窒素原子又はリン原子を示す。]で表されるオニウム塩又は式(3):
(式中、環Aは5又は6員環の芳香族環を示し、環を構成する原子に窒素原子、酸素原子又は硫黄原子を含んでいても良い。R1、R2及びYは前記に同じ。)で表されるオニウム塩を導電性付与物質として含有することを特徴とする樹脂組成物用帯電防止剤。
【選択図】なし
Description
(R1R2R3R4Y)+・(CF3SO2)2N− (1)
[式中、R1、R2、R3及びR4はそれぞれ互いに同じであっても異なっていてもよく、アルキル基、アルケニル基又は式(2):
(式中、R5はメチル基又はエチル基を示す。)で表されるアルキルオキシエトキシエチル基を示し、R1、R2、R3及びR4のいずれか二つが末端で互いに結合してアルキレン鎖を形成していてもよい。Yは窒素原子又はリン原子を示す。]で表されるオニウム塩[以下、オニウム塩(1)という。]又は式(3):
式(1)及び式(3)中、R1、R2、R3及びR4で示されるアルキル基としては特に限定されないが、置換基を有していても良い炭素数1〜18の直鎖状、分岐鎖状若しくは環状のアルキル基である。具体的には、例えばメチル基、エチル基、プロピル基、イソプロピル基、ブチル基、イソブチル基、sec−ブチル基、tert−ブチル基、ペンチル基、ペンチル基、ネオペンチル基、ヘキシル基、イソヘキシル基、デシル基、ドデシル基、オクタデシル基、シクロペンチル基、シクロヘキシル基等が挙げられる。アルケニル基としては置換基を有していても良い炭素数2〜6の直鎖状又は分岐鎖状のアルケニル基が挙げられ、具体的には、例えばビニル基、アリル基等が挙げられる。また、R1、R2、R3及びR4のうち少なくとも一つが、炭素数8〜12の直鎖又は分岐鎖のアルキル基、アリル基若しくは式(2)で表されるアルキルオキシエトキシエチル基であることが好ましい。R1、R2、R3及びR4のいずれか二つが末端で互いに結合して形成されるアルキレン鎖としては、テトラメチレン基、ペンタメチレン基等が挙げられる。テトラメチレン基の場合、それとオニウム塩のカチオンを構成する窒素原子とでピロリジン環を、或いはオニウム塩のカチオンを構成するリン原子とでホスフォラン環を形成する。またペンタメチレン基の場合、それとオニウム塩のカチオンを構成する窒素原子とでピペリジン環を、或いはオニウム塩のカチオンを構成するリン原子とでホスフォリナン環を形成する。置換基としては、例えば水酸基、アミノ基、アルコキシ基、アリール基等が挙げられる。
二液架橋型アクリル系粘着剤(東亞合成化学株式会社製アロンタックTT−1000:登録商標)100重量部、これに本発明の樹脂組成物用帯電防止剤であるN−メチル−N,N,N−トリオクチルアンモニウム=ビス(トリフルオロメタンスルホニル)イミダートを3重量部、アクリル樹脂用硬化剤(綜研化学株式会社製L−45)を0.2重量部、希釈溶剤として酢酸エチル/メチルエチルケトン(50/50)150重量部を添加して粘着剤コート液を調整した。本コート液をポリエステルフィルム上にバーコーダを用いて乾燥厚み約10μmの厚みでコートし、80℃で2分間加熱硬化させて粘着剤評価用サンプルを作成した。
実施例1のN−メチル−N,N,N−トリオクチルアンモニウム=ビス(トリフルオロメタンスルホニル)イミダートの代わりに表1に示す樹脂組成物用帯電防止剤を用い、実施例1と同様にして評価用サンプルを作成した。
エコハートS(登録商標:都インキ株式会社製)100重量部、これに本発明の樹脂組成物用帯電防止剤であるN−メチル−N,N,N−トリオクチルアンモニウム=ビス(トリフルオロメタンスルホニル)イミダートを3重量部、希釈溶剤としてトルエン25重量部を添加してコート用インキメジウム液を調整した。本メジウム液をバーコーダを用いてポリエステルフィルム上に乾燥厚み約0.3μmの厚みでコートし、熱風乾燥して評価用サンプルを作成した。
実施例5のN−メチル−N,N,N−トリオクチルアンモニウム=ビス(トリフルオロメタンスルホニル)イミダートの代わりに表3に示す樹脂組成物用帯電防止剤を用い、実施例5と同様にして評価用サンプルを作成した。
エポキシ樹脂としてエピコート828(ビスフェノールA型エポキシ樹脂、エポキシ当量 186g/eq、登録商標:ジャパンエポキシレジン株式会社製)100重量部、硬化剤としてイミノビスプロピルアミンを14.1重量部及び本発明の樹脂組成物用帯電防止剤であるN,N−ジアリル−N−ヘキシル−N−メチルアンモニウム=ビス(トリフルオロメタンスルホニル)イミダート5.7重量部(配合樹脂に対して5%)を混合し、エポキシ樹脂組成物とした。かかるエポキシ樹脂組成物を50mm×50mm×深さ5mmの金型に流し込み、50℃にて1時間、さらに100℃6時間保持し、熱硬化させて評価用サンプルを作成した。
実施例9のN,N−ジアリル−N−ヘキシル−N−メチルアンモニウム=ビス(トリフルオロメタンスルホニル)イミダートに代えて表5に示す樹脂組成物用帯電防止剤を用い、実施例9と同様にして評価用サンプルを作成した。
実施例9のN,N−ジアリル−N−ヘキシル−N−メチルアンモニウム=ビス(トリフルオロメタンスルホニル)イミダートを用いない以外は実施例9と同様にして評価用サンプルを作成した。
Claims (4)
- 式(1):
(R1R2R3R4Y)+・(CF3SO2)2N− (1)
[式中、R1、R2、R3及びR4はそれぞれ互いに同じであっても異なっていてもよく、アルキル基、アルケニル基又は式(2):
R5OCH2CH2OCH2CH2− (2)
(式中、R5はメチル基又はエチル基を示す。)で表されるアルキルオキシエトキシエチル基を示し、R1、R2、R3及びR4のいずれか二つが末端で互いに結合してアルキレン鎖を形成していてもよい。Yは窒素原子又はリン原子を示す。]で表されるオニウム塩又は式(3):
- 請求項1記載の樹脂組成物用帯電防止剤を含有してなる樹脂組成物。
- 樹脂組成物が粘着剤である請求項2記載の樹脂組成物。
- 樹脂組成物がインキである請求項2記載の樹脂組成物。
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