{"id":5131,"date":"2022-03-14T12:55:14","date_gmt":"2022-03-14T12:55:14","guid":{"rendered":"https:\/\/longchangchemical.com\/?p=5131"},"modified":"2024-12-11T15:34:31","modified_gmt":"2024-12-11T15:34:31","slug":"research-on-the-principle-and-application-of-uv-monomer-inhibitor","status":"publish","type":"post","link":"https:\/\/longchangchemical.com\/hu\/research-on-the-principle-and-application-of-uv-monomer-inhibitor\/","title":{"rendered":"Az UV-monomer inhibitor elv\u00e9nek \u00e9s alkalmaz\u00e1s\u00e1nak kutat\u00e1sa"},"content":{"rendered":"

1. Az UV-monomer polimeriz\u00e1ci\u00f3s blokkol\u00f3 meghat\u00e1roz\u00e1sa<\/h2>\n

Olyan anyag, amely k\u00e9pes teljesen megsz\u00fcntetni az alk\u00e9n-monomerek szabadgy\u00f6k\u00f6s polimeriz\u00e1ci\u00f3s reakci\u00f3j\u00e1t.<\/p>\n

2. A polimeriz\u00e1ci\u00f3s inhibitorok szerepe<\/h2>\n

A tel\u00edtetlen vegy\u00fcletrendszerben a polimeriz\u00e1ci\u00f3s inhibitor el\u0151ny\u00f6sen k\u00f6lcs\u00f6nhat\u00e1sba l\u00e9phet a rendszerben l\u00e9v\u0151 szabadgy\u00f6k\u00f6kkel, hogy nem-gy\u00f6k\u00f6ket vagy alacsony aktivit\u00e1s\u00fa gy\u00f6k\u00f6ket k\u00e9pezzen, amelyek nem elegend\u0151ek az \u00fajraindul\u00e1shoz, \u00e9s hat\u00e9konyan blokkolhatja a szabadgy\u00f6k\u00f6k l\u00e1ncpolimeriz\u00e1ci\u00f3j\u00e1t.
\nHat\u00e9konyan blokkolhatja a szabad gy\u00f6k\u00f6k l\u00e1ncpolimeriz\u00e1ci\u00f3j\u00e1t. Nagy el\u0151nyei vannak a gyanta stabilit\u00e1sa, t\u00e1rol\u00e1sa \u00e9s sz\u00e1ll\u00edt\u00e1sa szempontj\u00e1b\u00f3l.
\nBlokkol\u00e1si mechanizmus: A polimeriz\u00e1ci\u00f3s reakci\u00f3 g\u00e1tl\u00e1s\u00e1ban bet\u00f6lt\u00f6tt szerepe szerint azokat az anyagokat, amelyek k\u00e9pesek megsz\u00fcntetni az egyes gy\u00f6k\u00f6ket \u00e9s le\u00e1ll\u00edtani a polimeriz\u00e1ci\u00f3s reakci\u00f3t, am\u00edg azok teljesen ki nem mer\u00fclnek, blokkol\u00f3knak vagy inhibitoroknak nevezz\u00fck;
\n\u00c9s csak a szabadgy\u00f6k-aktivit\u00e1st gyeng\u00edti, lass\u00edtja a polimeriz\u00e1ci\u00f3s reakci\u00f3t, de nem tudja megsz\u00fcntetni a blokkol\u00f3knak nevezett anyagok reakci\u00f3j\u00e1t.<\/p>\n

3.UV monomer a polimeriz\u00e1ci\u00f3s inhibitorok oszt\u00e1lyoz\u00e1s\u00e1nak mechanizmusa szerint<\/h2>\n

3.1. Fenolos polimeriz\u00e1ci\u00f3s inhibitorok<\/h3>\n

a. Hidrokinon
\nGyakrabban haszn\u00e1lt, alacsony \u00e1r, jobb hat\u00e1s szobah\u0151m\u00e9rs\u00e9kleten.
\nDe n\u00e9ha a rendszer sz\u00edn\u00e9nek s\u00f6t\u00e9ted\u00e9s\u00e9t okozza, gyakran nem haszn\u00e1lj\u00e1k.
\nb. Para-hidroxianizol
\nJ\u00f3 t\u00e1rol\u00e1si stabilit\u00e1st biztos\u00edthat a gyant\u00e1nak. A term\u00e9k oldhat\u00f3s\u00e1ga szerves old\u00f3szerekben Z j\u00f3, a term\u00e9k sz\u00edne Z vil\u00e1gos.
\nc.2,6-Di-terc-butil-p-metilfenol
\nSz\u00e9les k\u00f6rben haszn\u00e1lt polimeriz\u00e1ci\u00f3s inhibitor, er\u0151s polimeriz\u00e1ci\u00f3s g\u00e1tl\u00f3 k\u00e9pess\u00e9g, j\u00f3 h\u0151\u00e1ll\u00f3s\u00e1g \u00e9s stabilit\u00e1s, alacsony \u00e1r.
\nA toxicit\u00e1s nagyobb.
\nd.2,5-di-terc-butil-hidrokinon
\nHossz\u00fa id\u0151n kereszt\u00fcl lassan reag\u00e1lhat a szabad gy\u00f6k\u00f6kkel, hogy elpuszt\u00edtsa a gyanta t\u00e1rol\u00e1sa sor\u00e1n keletkezett szabad gy\u00f6k\u00f6ket.
\nJav\u00edthatja a gyanta t\u00e1rol\u00e1si stabilit\u00e1s\u00e1t, mik\u00f6zben kev\u00e9s hat\u00e1ssal van a zsel\u00e9sed\u00e9si id\u0151re.
\ne.2-tert-butil-hidrokinon
\nA tel\u00edtetlen poli\u00e9sztergyant\u00e1k hat\u00e9kony t\u00e1rol\u00e1si stabiliz\u00e1tora, valamint a nagy reakci\u00f3k\u00e9pess\u00e9g\u0171 gyant\u00e1k stabiliz\u00e1tora.
\nFunkci\u00f3ja \u00e1tfog\u00f3, \u00e9s a h\u0151m\u00e9rs\u00e9klet sz\u00e9les sk\u00e1l\u00e1j\u00e1n j\u00f3 szerepet j\u00e1tszhat. \u00c9s csak kiss\u00e9 meghosszabb\u00edtja a gyanta kikem\u00e9nyed\u00e9s\u00e9t magas h\u0151m\u00e9rs\u00e9kleten. Ezt a term\u00e9ket gyakran m\u00e1s polimeriz\u00e1ci\u00f3s inhibitorokkal kombin\u00e1lva haszn\u00e1lj\u00e1k.
\nJellemz\u0151k:Sz\u00e9les k\u00f6rben haszn\u00e1lt \u00e9s hat\u00e9kony. Fel kell oldani a rendszerben, \u00e9s az oxig\u00e9n jelenl\u00e9t\u00e9ben a polimeriz\u00e1ci\u00f3s g\u00e1tl\u00e1s hat\u00e1s\u00e1nak kimutat\u00e1s\u00e1hoz.<\/p>\n

3.2. Kinon-polimeriz\u00e1ci\u00f3s inhibitorok<\/h3>\n

a. P-benzokinon
\nAz UV-monomer oxig\u00e9n hi\u00e1ny\u00e1ban is k\u00e9pes m\u0171k\u00f6dni, alkalmas nitrog\u00e9nnel vagy m\u00e1s inert g\u00e1zzal v\u00e9dett \u00e9teres\u00edt\u00e9si folyamathoz.
\nS\u00e1rga sz\u00edn, hat\u00e1ssal van a gyanta sz\u00edn\u00e9re.
\nb.Metil-hidrokinon (THQ)
\nJ\u00f3 hat\u00e1s\u00fa, nagy aktivit\u00e1s\u00fa tel\u00edtetlen poli\u00e9sztergyanta gy\u00e1rt\u00e1s\u00e1hoz haszn\u00e1lt, \u00e1ltal\u00e1ban g\u00e9lbevonat\u00fa gyant\u00e1ban, SMC-gyant\u00e1ban haszn\u00e1lt. Ez a term\u00e9k j\u00f3 oldhat\u00f3s\u00e1ggal \u00e9s j\u00f3 magas h\u0151m\u00e9rs\u00e9klet\u0171 polimeriz\u00e1ci\u00f3s blokkol\u00f3 hat\u00e1ssal rendelkezik.
\nc.Egy\u00e9b kinon-polimeriz\u00e1ci\u00f3s inhibitorok
\nJellemz\u0151k: Szerepet j\u00e1tszhat a polimeriz\u00e1ci\u00f3 megakad\u00e1lyoz\u00e1s\u00e1ban anaerob k\u00f6r\u00fclm\u00e9nyek k\u00f6z\u00f6tt.
\nA polikondenz\u00e1ci\u00f3t g\u00e1tl\u00f3 hat\u00e1s k\u00fcl\u00f6nb\u00f6z\u0151 monomerek eset\u00e9n elt\u00e9r\u0151
\np\u00e9lda: A p-benzokinon hat\u00e9kony polimeriz\u00e1ci\u00f3s inhibitor a sztirol \u00e9s a vinil-acet\u00e1t eset\u00e9ben, de csak a metil-akril\u00e1t \u00e9s a metil-metakril\u00e1t eset\u00e9ben hat k\u00e9sleltet\u0151szerk\u00e9nt.
\n2. p\u00e9lda: A tetrakl\u00f3r-benzokinon hat\u00e9kony polimeriz\u00e1ci\u00f3g\u00e1tl\u00f3 a vinil-acet\u00e1t eset\u00e9ben, de nincs polimeriz\u00e1ci\u00f3g\u00e1tl\u00f3 hat\u00e1sa az akrilnitrilre.
\nA polimeriz\u00e1ci\u00f3 blokkol\u00e1s\u00e1nak mechanizmusa: A kinon polimeriz\u00e1ci\u00f3 blokkol\u00e1s\u00e1nak mechanizmusa nem teljesen vil\u00e1gos, lehet, hogy a kinon \u00e9s a szabad gy\u00f6k\u00f6k add\u00edci\u00f3s vagy disproportion\u00e1ci\u00f3s reakci\u00f3t v\u00e9geznek, hogy kinon t\u00edpus\u00fa vagy f\u00e9lkinon t\u00edpus\u00fa szabad gy\u00f6k\u00f6ket hozzanak l\u00e9tre, majd akt\u00edv szabad gy\u00f6k\u00f6kkel egyes\u00fclve inakt\u00edv term\u00e9keket kapnak, amelyek szerepet j\u00e1tszanak a polimeriz\u00e1ci\u00f3 blokkol\u00e1s\u00e1ban.<\/p>\n

3.3. Arom\u00e1s nitrovegy\u00fcletek polimeriz\u00e1ci\u00f3s inhibitorok<\/h3>\n

\u00c1ltal\u00e1nosan haszn\u00e1ltak a k\u00f6vetkez\u0151k
\nJellemz\u0151k: Az arom\u00e1s nitrovegy\u00fcletek nem olyan hat\u00e9konyak a polimeriz\u00e1ci\u00f3 blokkol\u00e1s\u00e1ban, mint a fenolok.
\nCsak vinil-acet\u00e1t, izopr\u00e9n, butadi\u00e9n, sztirol eset\u00e9n haszn\u00e1lhat\u00f3, akril\u00e1tokra \u00e9s metakril\u00e1tokra nincs blokkol\u00f3 hat\u00e1sa.
\nA polimeriz\u00e1ci\u00f3 g\u00e1tl\u00e1s\u00e1nak mechanizmusa: A nitrobenzol polimeriz\u00e1ci\u00f3s inhibitork\u00e9nt hat az\u00e1ltal, hogy a szabad gy\u00f6k\u00f6kkel stabil nitroxidgy\u00f6k\u00f6ket hoz l\u00e9tre.<\/p>\n

3.4. Szervetlen vegy\u00fcletek polimeriz\u00e1ci\u00f3s inhibitorok<\/h3>\n

Gyakran haszn\u00e1lj\u00e1k a vas-kloridot, a r\u00e9z-kloridot, a r\u00e9z-szulf\u00e1tot, a tit\u00e1n-trikloridot, a n\u00e1trium-szulf\u00e1tot, az amm\u00f3nium-tiocian\u00e1tot.
\nJellemz\u0151k: nagy hat\u00e9konys\u00e1g\u00fa polimeriz\u00e1ci\u00f3, \u00e9s vizes f\u00e1zis\u00fa polimeriz\u00e1ci\u00f3s inhibitork\u00e9nt alkalmazhat\u00f3
\nA koaleszcencia blokkol\u00e1s\u00e1nak mechanizmusa: koaleszcencia blokkol\u00e1sa t\u00f6lt\u00e9s\u00e1tad\u00e1ssal<\/p>\n

3.5.Oxig\u00e9n polimeriz\u00e1ci\u00f3s blokkol\u00f3 hat\u00e1s<\/h3>\n

A molekul\u00e1ris oxig\u00e9nnek k\u00e9t p\u00e1ros\u00edtatlan elektronja van, ami kett\u0151s szerepet j\u00e1tszhat a polimeriz\u00e1ci\u00f3 g\u00e1tl\u00e1s\u00e1ban \u00e9s beind\u00edt\u00e1s\u00e1ban.
\nBlokkol\u00f3 mechanizmus: R-+O2 \u2192ROO -
\nA peroxid gy\u00f6k\u00f6k \u00e1ltal gener\u00e1lt oxig\u00e9n \u00e9s makromolekul\u00e1ris l\u00e1ncgy\u00f6k\u00f6k inakt\u00edvabbak, szobah\u0151m\u00e9rs\u00e9kleten vagy valamivel magasabb h\u0151m\u00e9rs\u00e9kleten nem tudj\u00e1k kiv\u00e1ltani a kopolimeriz\u00e1ci\u00f3s reakci\u00f3t, ez az oxig\u00e9n blokkol\u00f3 hat\u00e1sa miatt a tel\u00edtetlen poli\u00e9sztergyanta \u00e9s a leveg\u0151vel \u00e9rintkez\u0151 fel\u00fclet gy\u00f3gy\u00edt\u00e1sa hi\u00e1nyos \u00e9s ragacsos.
\nMagas h\u0151m\u00e9rs\u00e9kleten azonban az oxig\u00e9n \u00e9s a szabad gy\u00f6k\u00f6k \u00e1ltal gener\u00e1lt peroxidgy\u00f6k\u00f6k reakt\u00edv gy\u00f6k\u00f6kk\u00e9 bomolhatnak, \u00edgy beind\u00edtva a polimeriz\u00e1ci\u00f3s reakci\u00f3t.<\/p>\n

4, a polimeriz\u00e1ci\u00f3s inhibitorok egy\u00e9b oszt\u00e1lyoz\u00e1sai<\/h2>\n

4.1. H\u0151m\u00e9rs\u00e9klet szerint oszt\u00e1lyozva<\/h3>\n

4.2. Elv szerinti oszt\u00e1lyoz\u00e1s<\/h3>\n

4.3. \u00d6sszet\u00e9tel szerint oszt\u00e1lyozva<\/h3>\n

 <\/p>\n

5\u3001A polimeriz\u00e1ci\u00f3s inhibitor szelekt\u00edv m\u00f3dszere<\/h2>\n

A polimeriz\u00e1ci\u00f3s inhibitor kiv\u00e1laszt\u00e1s\u00e1nak f\u0151 k\u00f6vetelm\u00e9nye a magas polimeriz\u00e1ci\u00f3s blokkol\u00f3 hat\u00e9konys\u00e1g, figyelembe kell venni a rendszerben val\u00f3 oldhat\u00f3s\u00e1g\u00e1t \u00e9s a gyanta alkalmazkod\u00f3k\u00e9pess\u00e9g\u00e9t is.
\nN\u00e9h\u00e1ny nem f\u00e9nykem\u00e9nyed\u0151 rendszerben haszn\u00e1lt monomer is megk\u00f6veteli, hogy a monomer a rezisztben k\u00f6nnyen elt\u00e1vol\u00edthat\u00f3 desztill\u00e1ci\u00f3val vagy k\u00e9miai m\u00f3dszerekkel, vagy mindkett\u0151 szobah\u0151m\u00e9rs\u00e9kleten szerepet j\u00e1tszik a rezisztben, de a reakci\u00f3h\u0151m\u00e9rs\u00e9kleten is, amikor a gyors boml\u00e1s.<\/p>\n

5.1. J\u00f3 keverhet\u0151s\u00e9g monomerekkel \u00e9s gyant\u00e1kkal, csak keverhet\u0151 szerepet j\u00e1tszhat a blokkol\u00e1sban.<\/p>\n

5.2. Hat\u00e9konyan megakad\u00e1lyozhatja a polimeriz\u00e1ci\u00f3s reakci\u00f3 kialakul\u00e1s\u00e1t, \u00edgy a monomer, a gyanta, az emulzi\u00f3 vagy a ragaszt\u00f3 elegend\u0151 t\u00e1rol\u00e1si id\u0151vel rendelkezik.<\/p>\n

5.3. A polimeriz\u00e1ci\u00f3s inhibitor a monomerben k\u00f6nnyen elt\u00e1vol\u00edthat\u00f3, vagy nem befoly\u00e1solja a polimeriz\u00e1ci\u00f3s aktivit\u00e1st. z j\u00f3 v\u00e1laszt\u00e1s a szobah\u0151m\u00e9rs\u00e9kleten hat\u00e9kony inhibitor, \u00e9s megfelel\u0151en magas h\u0151m\u00e9rs\u00e9kleten elvesz\u00edti az inhibitort, \u00edgy nem kell elt\u00e1vol\u00edtani az inhibitort haszn\u00e1lat el\u0151tt.
\nP\u00e9ld\u00e1ul a tert-butil-katechol, p-fenol-monobutil-\u00e9ter ilyen t\u00edpus\u00fa polimeriz\u00e1ci\u00f3s inhibitor.<\/p>\n

5.4.UV monomer nem befoly\u00e1solja a megjelen\u00e9s\u00e9t a Z v\u00e9gterm\u00e9k.P\u00e9ld\u00e1ul a polimeriz\u00e1ci\u00f3s inhibitor a ragaszt\u00f3k el\u0151\u00e1ll\u00edt\u00e1sa sor\u00e1n az oxid\u00e1ci\u00f3 folyamat\u00e1ban a magas h\u0151m\u00e9rs\u00e9klet elsz\u00ednez\u0151d\u00e9s miatt, \u00e9s befoly\u00e1solja a term\u00e9k megjelen\u00e9s\u00e9t.<\/p>\n

5.5. T\u00f6bb polimeriz\u00e1ci\u00f3s inhibitor egym\u00e1ssal egy\u00fctt alkalmazva jelent\u0151sen jav\u00edthatja a polimeriz\u00e1ci\u00f3 hat\u00e1s\u00e1t.<\/p>\n

P\u00e9lda 1: tel\u00edtetlen poli\u00e9szter gyanta hozz\u00e1ad\u00e1s\u00e1val hidrokinon, tert-butil-katechol \u00e9s r\u00e9z-naft\u00e9n\u00e1t h\u00e1romf\u00e9le inhibitorok.Z er\u0151s aktivit\u00e1sa hidrokinon, keverhet\u0151 sztirol \u00e9s poli\u00e9szter ellen\u00e1ll magas h\u0151m\u00e9rs\u00e9kleten k\u00f6r\u00fclbel\u00fcl 130 \u2103, 1 percen bel\u00fcl nem rendelkezik kopolimeriz\u00e1ci\u00f3s hat\u00e1s, lehet biztons\u00e1gosan kevert h\u00edg\u00edt\u00e1s.
\nTert-butil-katechol magas h\u0151m\u00e9rs\u00e9kleten, a blokkol\u00f3 hat\u00e1s nagyon gyenge, de egy kicsit alacsonyabb h\u0151m\u00e9rs\u00e9kleten (p\u00e9ld\u00e1ul 60 \u2103, amikor), a blokkol\u00f3 hat\u00e1s 25-sz\u00f6r nagyobb, mint a hidrokinon, lehet egy hosszabb t\u00e1rol\u00e1si id\u0151szak, r\u00e9z-naft\u00e9n\u00e1t szobah\u0151m\u00e9rs\u00e9kleten j\u00e1tszani egy blokkol\u00f3 hat\u00e1s, \u00e9s a magas h\u0151m\u00e9rs\u00e9klet \u00e9s el\u0151seg\u00edti a szerepet.
\nP\u00e9lda 2: Oxig\u00e9n jelenl\u00e9t\u00e9ben. A fenotiazinnal, hidrokinonnal \u00e9s difenil-aminnal kevert p-tert-butil-katechol blokkol\u00f3 hat\u00e1sa k\u00f6r\u00fclbel\u00fcl 300-szor nagyobb, mint b\u00e1rmelyik\u00e9 \u00f6nmag\u00e1ban.<\/p>\n

5.6.UV monomer polimeriz\u00e1ci\u00f3s inhibitor adagol\u00e1s megfelel\u0151, t\u00f6bb k\u00e1ros.<\/p>\n

P\u00e9ld\u00e1ul a 10-4 mol\/l j\u00f3dadagol\u00e1s hat\u00e9kony polimeriz\u00e1ci\u00f3s inhibitor, de enn\u00e9l nagyobb mennyis\u00e9g kiv\u00e1ltja a polimeriz\u00e1ci\u00f3s reakci\u00f3t. A j\u00f3dot \u00e1ltal\u00e1ban nem haszn\u00e1lj\u00e1k \u00f6nmag\u00e1ban, kis mennyis\u00e9g\u0171 k\u00e1lium-jodidot kell hozz\u00e1adni az oldhat\u00f3s\u00e1g n\u00f6vel\u00e9se \u00e9s a polimeriz\u00e1ci\u00f3 hat\u00e9konys\u00e1g\u00e1nak jav\u00edt\u00e1sa \u00e9rdek\u00e9ben.<\/p>\n

5.7.UV monomer nem m\u00e9rgez\u0151, \u00e1rtalmatlan, nincs k\u00f6rnyezetszennyez\u00e9s<\/p>\n

5.8. Stabil teljes\u00edtm\u00e9ny, olcs\u00f3 \u00e9s k\u00f6nnyen beszerezhet\u0151<\/p>\n

 <\/p>\n

6. Gondolkodj<\/h2>\n

Milyen hat\u00e1ssal van az inici\u00e1tor, a reduk\u00e1l\u00f3szer \u00e9s a polimeriz\u00e1ci\u00f3s inhibitor tartalma a gyanta kem\u00e9nyed\u00e9s\u00e9re \u00e9s teljes\u00edtm\u00e9ny\u00e9re?
\nP\u00e9lda: UV-monomer k\u00eds\u00e9rleti anyagok
\nK\u00eds\u00e9rleti m\u00f3dszer: UV monomer, illetve v\u00e1ltoztassa meg az inici\u00e1tor, az amin \u00e9s a redukt\u00e1ns tartalm\u00e1t a kett\u0151s k\u00f6t\u00e9s \u00e1talakul\u00e1s\u00e1nak, mechanikai tulajdons\u00e1gainak \u00e9s a gyanta kem\u00e9nyed\u00e9si sebess\u00e9g\u00e9nek vizsg\u00e1lat\u00e1hoz \u00e9s \u00f6sszehasonl\u00edt\u00e1s\u00e1hoz.
\nA gyant\u00e1hoz hozz\u00e1adott inici\u00e1tor, amin \u00e9s polimeriz\u00e1ci\u00f3s inhibitor k\u00fcl\u00f6nb\u00f6z\u0151 tartalmainak t\u00e1bl\u00e1zata a k\u00f6vetkez\u0151.
\nK\u00eds\u00e9rleti eredm\u00e9nyek.<\/p>\n

Egy bizonyos tartom\u00e1nyon bel\u00fcl az UV-monomer gyant\u00e1k konverzi\u00f3s foka \u00e9s mechanikai tulajdons\u00e1gai pozit\u00edvan korrel\u00e1ltak a BPO- \u00e9s DEPT-tartalommal, \u00e9s negat\u00edvan korrel\u00e1ltak a reziszt-tartalommal.
\nA BPO \u00e9s a DEPT tartalm\u00e1nak n\u00f6vel\u00e9se n\u00f6velheti a gyanta kem\u00e9nyed\u00e9si sebess\u00e9g\u00e9t, a reziszt tartalm\u00e1nak n\u00f6vel\u00e9se pedig cs\u00f6kkenti a gyanta kem\u00e9nyed\u00e9si sebess\u00e9g\u00e9t.<\/p>\n

 <\/p>\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n
Politiol\/Polimerkapt\u00e1n<\/strong><\/td>\n<\/td>\n<\/td>\n<\/tr>\n
DMES monomer<\/a><\/span><\/td>\nBis(2-merkaptoetil)szulfid<\/td>\n3570-55-6<\/td>\n<\/tr>\n
DMPT monomer<\/a><\/span><\/td>\nTHIOCURE DMPT<\/td>\n131538-00-6<\/td>\n<\/tr>\n
PETMP monomer<\/a><\/span><\/td>\nPENTAERITRITOL-TETRA(3-MERKAPTOPROPION\u00c1T)<\/td>\n7575-23-7<\/td>\n<\/tr>\n
PM839 Monomer<\/a><\/span><\/td>\nPolioxi(metil-1,2-et\u00e1ndiil)<\/td>\n72244-98-5<\/td>\n<\/tr>\n
Monofunkci\u00f3s monomer<\/strong><\/td>\n<\/td>\n<\/td>\n<\/tr>\n
HEMA monomer<\/a><\/span><\/td>\n2-hidroxietil-metakril\u00e1t<\/td>\n868-77-9<\/td>\n<\/tr>\n
HPMA monomer<\/a><\/span><\/td>\n2-hidroxipropil-metakril\u00e1t<\/td>\n27813-02-1<\/td>\n<\/tr>\n
THFA monomer<\/a><\/span><\/td>\nTetrahidrofurfuril-akril\u00e1t<\/td>\n2399-48-6<\/td>\n<\/tr>\n
HDCPA monomer<\/a><\/span><\/td>\nHidrog\u00e9nezett diciklopentenil-akril\u00e1t<\/td>\n79637-74-4<\/td>\n<\/tr>\n
DCPMA monomer<\/a><\/span><\/td>\nDihidrodiciklopentadienil-metakril\u00e1t<\/td>\n30798-39-1<\/td>\n<\/tr>\n
DCPA monomer<\/a><\/span><\/td>\nDihidrodiciklopentadienil-akril\u00e1t<\/td>\n12542-30-2<\/td>\n<\/tr>\n
DCPEMA monomer<\/a><\/span><\/td>\nDiciklopenteniloxi-etil-metakril\u00e1t<\/td>\n68586-19-6<\/td>\n<\/tr>\n
DCPEOA monomer<\/a><\/span><\/td>\nDiciklopenteniloxi-etil-akril\u00e1t<\/td>\n65983-31-5<\/td>\n<\/tr>\n
NP-4EA monomer<\/a><\/span><\/td>\n(4) etoxil\u00e1lt nonylfenol<\/td>\n50974-47-5<\/td>\n<\/tr>\n
LA Monomer<\/td>\nLauril-akril\u00e1t \/ dodecil-akril\u00e1t<\/td>\n2156-97-0<\/td>\n<\/tr>\n
THFMA monomer<\/a><\/span><\/td>\nTetrahidrofurfuril-metakril\u00e1t<\/td>\n2455-24-5<\/td>\n<\/tr>\n
PHEA monomer<\/span><\/a><\/td>\n2-FENOXI-ETIL-AKRIL\u00c1T<\/td>\n48145-04-6<\/td>\n<\/tr>\n
LMA monomer<\/a><\/span><\/td>\nLauril-metakril\u00e1t<\/td>\n142-90-5<\/td>\n<\/tr>\n
IDA monomer<\/a><\/span><\/td>\nIzodecil-akril\u00e1t<\/td>\n1330-61-6<\/td>\n<\/tr>\n
IBOMA monomer<\/a><\/span><\/td>\nIzobornyl-metakril\u00e1t<\/td>\n7534-94-3<\/td>\n<\/tr>\n
IBOA monomer<\/a><\/span><\/td>\nIzobornyil-akril\u00e1t<\/td>\n5888-33-5<\/td>\n<\/tr>\n
EOEOEA Monomer<\/a><\/span><\/td>\n2-(2-etoxietoxi-etoxi)etil-akril\u00e1t<\/td>\n7328-17-8<\/td>\n<\/tr>\n
Multifunkcion\u00e1lis monomer<\/strong><\/td>\n<\/td>\n<\/td>\n<\/tr>\n
DPHA monomer<\/a><\/span><\/td>\nDipentaeritritol-hexakril\u00e1t<\/td>\n29570-58-9<\/td>\n<\/tr>\n
DI-TMPTA monomer<\/a><\/span><\/td>\nDI(TRIMETILOLPROPAN)TETRAAKRIL\u00c1T<\/td>\n94108-97-1<\/td>\n<\/tr>\n
Akrilamid-monomer<\/strong><\/td>\n<\/td>\n<\/td>\n<\/tr>\n
ACMO monomer<\/a><\/span><\/td>\n4-akrilil-morfolin<\/td>\n5117-12-4<\/td>\n<\/tr>\n
Difunkci\u00f3s monomer<\/strong><\/td>\n<\/td>\n<\/td>\n<\/tr>\n
PEGDMA monomer<\/a><\/span><\/td>\nPoli(etil\u00e9nglikol)-dimetakril\u00e1t<\/td>\n25852-47-5<\/td>\n<\/tr>\n
TPGDA monomer<\/a><\/span><\/td>\nTripropil\u00e9n-glikol-diacril\u00e1t<\/td>\n42978-66-5<\/td>\n<\/tr>\n
TEGDMA monomer<\/a><\/span><\/td>\nTrietil\u00e9nglikol-dimetakril\u00e1t<\/td>\n109-16-0<\/td>\n<\/tr>\n
PO2-NPGDA monomer<\/span><\/a><\/td>\nPropoxil\u00e1t neopentylenglikol-diacril\u00e1t<\/td>\n84170-74-1<\/td>\n<\/tr>\n
PEGDA monomer<\/a><\/span><\/td>\nPolietil\u00e9n-glikol-diacril\u00e1t<\/td>\n26570-48-9<\/td>\n<\/tr>\n
PDDA monomer<\/a><\/span><\/td>\nFtal\u00e1t dietil\u00e9nglikol-diacril\u00e1t<\/td>\n<\/td>\n<\/tr>\n
NPGDA monomer<\/a><\/span><\/td>\nNeopentil-glikol-diacril\u00e1t<\/td>\n2223-82-7<\/td>\n<\/tr>\n
HDDA monomer<\/a><\/span><\/td>\nHexametil\u00e9n-diacril\u00e1t<\/td>\n13048-33-4<\/td>\n<\/tr>\n
EO4-BPADA monomer<\/span><\/a><\/td>\nETOXIL\u00c1LT (4) BISZFENOL A-DIACRIL\u00c1T<\/td>\n64401-02-1<\/td>\n<\/tr>\n
EO10-BPADA Monomer<\/a><\/span><\/td>\nETOXIL\u00c1LT (10) BISZFENOL A-DIACRIL\u00c1T<\/td>\n64401-02-1<\/td>\n<\/tr>\n
EGDMA monomer<\/a><\/span><\/td>\nEtil\u00e9nglikol-dimetakril\u00e1t<\/td>\n97-90-5<\/td>\n<\/tr>\n
DPGDA monomer<\/a><\/span><\/td>\nDipropil\u00e9n-glikol-dieno\u00e1t<\/td>\n57472-68-1<\/td>\n<\/tr>\n
Bis-GMA monomer<\/a><\/span><\/td>\nBiszfenol A glicidil-metakril\u00e1t<\/td>\n1565-94-2<\/td>\n<\/tr>\n
Trifunkcion\u00e1lis monomer<\/strong><\/td>\n<\/td>\n<\/td>\n<\/tr>\n
TMPTMA monomer<\/a><\/span><\/td>\nTrimetilolpropan-trimetakril\u00e1t<\/td>\n3290-92-4<\/td>\n<\/tr>\n
TMPTA monomer<\/a><\/span><\/td>\nTrimetilolpropan-trikril\u00e1t<\/td>\n15625-89-5<\/td>\n<\/tr>\n
PETA monomer<\/a><\/span><\/td>\nPentaeritritol-trikril\u00e1t<\/td>\n3524-68-3<\/td>\n<\/tr>\n
GPTA ( G3POTA ) Monomer<\/a><\/span><\/td>\nGLICERIL-PROPOXI-TRIAKRIL\u00c1T<\/td>\n52408-84-1<\/td>\n<\/tr>\n
EO3-TMPTA monomer<\/a><\/span><\/td>\nEtoxil\u00e1lt trimetilolpropan-trikril\u00e1t<\/td>\n28961-43-5<\/td>\n<\/tr>\n
Fotoreziszt monomer<\/strong><\/td>\n<\/td>\n<\/td>\n<\/tr>\n
IPAMA monomer<\/a><\/span><\/td>\n2-izopropil-2-adamantil-metakril\u00e1t<\/td>\n297156-50-4<\/td>\n<\/tr>\n
ECPMA monomer<\/a><\/span><\/td>\n1-etil-ciklopentil-metakril\u00e1t<\/td>\n266308-58-1<\/td>\n<\/tr>\n
ADAMA monomer<\/a><\/span><\/td>\n1-Adamantil-metakril\u00e1t<\/td>\n16887-36-8<\/td>\n<\/tr>\n
Metakril\u00e1t monomer<\/strong><\/td>\n<\/td>\n<\/td>\n<\/tr>\n
TBAEMA monomer<\/a><\/span><\/td>\n2-(terc-butilamino)etil-metakril\u00e1t<\/td>\n3775-90-4<\/td>\n<\/tr>\n
NBMA monomer<\/a><\/span><\/td>\nn-butil-metakril\u00e1t<\/td>\n97-88-1<\/td>\n<\/tr>\n
MEMA monomer<\/a><\/span><\/td>\n2-metoxietil-metakril\u00e1t<\/td>\n6976-93-8<\/td>\n<\/tr>\n
i-BMA monomer<\/a><\/span><\/td>\nIzobutil-metakril\u00e1t<\/td>\n97-86-9<\/td>\n<\/tr>\n
EHMA monomer<\/a><\/span><\/td>\n2-etilhexil-metakril\u00e1t<\/td>\n688-84-6<\/td>\n<\/tr>\n
EGDMP monomer<\/a><\/span><\/td>\nEtil\u00e9nglikol bisz(3-merkaptopropion\u00e1t)<\/td>\n22504-50-3<\/td>\n<\/tr>\n
EEMA monomer<\/a><\/span><\/td>\n2-etoxietil-2-metilprop-2-eno\u00e1t<\/td>\n2370-63-0<\/td>\n<\/tr>\n
DMAEMA monomer<\/a><\/span><\/td>\nN,M-dimetil-aminoetil-metakril\u00e1t<\/td>\n2867-47-2<\/td>\n<\/tr>\n
DEAM monomer<\/a><\/span><\/td>\nDietilaminoetil-metakril\u00e1t<\/td>\n105-16-8<\/td>\n<\/tr>\n
CHMA monomer<\/a><\/span><\/td>\nCiklohexil-metakril\u00e1t<\/td>\n101-43-9<\/td>\n<\/tr>\n
BZMA monomer<\/a><\/span><\/td>\nBenzil-metakril\u00e1t<\/td>\n2495-37-6<\/td>\n<\/tr>\n
BDDMP monomer<\/a><\/span><\/td>\n1,4-But\u00e1ndiol Di(3-merkaptopropion\u00e1t)<\/td>\n92140-97-1<\/td>\n<\/tr>\n
BDDMA monomer<\/a><\/span><\/td>\n1,4-but\u00e1ndioldi-oldimetakril\u00e1t<\/td>\n2082-81-7<\/td>\n<\/tr>\n
AMA monomer<\/a><\/span><\/td>\nAlil-metakril\u00e1t<\/td>\n96-05-9<\/td>\n<\/tr>\n
AAEM monomer<\/a><\/span><\/td>\nAcetilacetoxi-etil-metakril\u00e1t<\/td>\n21282-97-3<\/td>\n<\/tr>\n
Akril\u00e1t monomer<\/strong><\/td>\n<\/td>\n<\/tr>\n
IBA monomer<\/a><\/span><\/td>\nIzobutil-akril\u00e1t<\/td>\n106-63-8<\/td>\n<\/tr>\n
EMA monomer<\/a><\/span><\/td>\nEtil-metakril\u00e1t<\/td>\n97-63-2<\/td>\n<\/tr>\n
DMAEA monomer<\/a><\/span><\/td>\nDimetil-aminoetil-akril\u00e1t<\/td>\n2439-35-2<\/td>\n<\/tr>\n
DEAEA monomer<\/a><\/span><\/td>\n2-(dietilamino)etil-prop-2-eno\u00e1t<\/td>\n2426-54-2<\/td>\n<\/tr>\n
CHA monomer<\/a><\/span><\/td>\nciklohexil prop-2-eno\u00e1t<\/td>\n3066-71-5<\/td>\n<\/tr>\n
BZA monomer<\/a><\/span><\/td>\nbenzil-prop-2-eno\u00e1t<\/td>\n2495-35-4<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

 <\/p>\n

L\u00e9pjen kapcsolatba vel\u00fcnk most!<\/b><\/strong><\/p>\n

Ha sz\u00fcks\u00e9ge van az uv monomerek COA, MSDS vagy TDS adataira, k\u00e9rj\u00fck, t\u00f6ltse ki el\u00e9rhet\u0151s\u00e9g\u00e9t az al\u00e1bbi \u0171rlapon, \u00e1ltal\u00e1ban 24 \u00f3r\u00e1n bel\u00fcl felvessz\u00fck \u00d6nnel a kapcsolatot. \u00d6n is k\u00fcldhet nekem e-mailt info@longchangchemical.com<\/a><\/span> munkaid\u0151ben ( 8:30-18:00 UTC+8 H.-Szombat ) vagy haszn\u00e1lja a weboldal \u00e9l\u0151 chatj\u00e9t, hogy azonnali v\u00e1laszt kapjon.<\/b><\/strong><\/h4>","protected":false},"excerpt":{"rendered":"

1. Az UV-monomer polimeriz\u00e1ci\u00f3s blokkol\u00f3 defin\u00edci\u00f3ja Olyan anyag, amely k\u00e9pes teljesen megsz\u00fcntetni az alk\u00e9n-monomerek szabadgy\u00f6k\u00f6s polimeriz\u00e1ci\u00f3s reakci\u00f3j\u00e1t. 2. A polimeriz\u00e1ci\u00f3s inhibitorok szerepe A tel\u00edtetlen vegy\u00fcletrendszerben a polimeriz\u00e1ci\u00f3s inhibitor el\u0151ny\u00f6sen k\u00f6lcs\u00f6nhat\u00e1sba l\u00e9phet a rendszerben l\u00e9v\u0151 szabad gy\u00f6k\u00f6kkel, hogy nem gy\u00f6k\u00f6ket k\u00e9pezzen, vagy alacsony aktivit\u00e1s\u00fa gy\u00f6k\u00f6ket k\u00e9pezzen, amelyek [...]<\/p>","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[114],"tags":[],"class_list":["post-5131","post","type-post","status-publish","format-standard","hentry","category-catalysts-chemical-auxiliary-agents"],"yoast_head":"\nResearch on the principle and application of UV monomer inhibitor - Longchang Chemical<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/longchangchemical.com\/hu\/research-on-the-principle-and-application-of-uv-monomer-inhibitor\/\" \/>\n<meta property=\"og:locale\" content=\"hu_HU\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Research on the principle and application of UV monomer inhibitor - Longchang Chemical\" \/>\n<meta property=\"og:description\" content=\"1. Definition of UV monomer polymerization blocker A substance that can completely terminate the free radical polymerization reaction of alkene monomers. 2. 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Definition of UV monomer polymerization blocker A substance that can completely terminate the free radical polymerization reaction of alkene monomers. 2. Role of polymerization inhibitors In the unsaturated compound system, the polymerization inhibitor can preferentially interact with the free radicals in the system to form non-radicals, or form radicals with low activity, which are […]","og_url":"https:\/\/longchangchemical.com\/hu\/research-on-the-principle-and-application-of-uv-monomer-inhibitor\/","og_site_name":"Longchang Chemical","article_published_time":"2022-03-14T12:55:14+00:00","article_modified_time":"2024-12-11T15:34:31+00:00","og_image":[{"width":1000,"height":1000,"url":"https:\/\/longchangchemical.com\/wp-content\/uploads\/2024\/02\/logo-jpeg.jpg","type":"image\/jpeg"}],"author":"Longchang Chemical","twitter_card":"summary_large_image","schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/longchangchemical.com\/research-on-the-principle-and-application-of-uv-monomer-inhibitor\/#article","isPartOf":{"@id":"https:\/\/longchangchemical.com\/research-on-the-principle-and-application-of-uv-monomer-inhibitor\/"},"author":{"name":"Longchang Chemical","@id":"https:\/\/longchangchemical.com\/#\/schema\/person\/ecb1ad846136c6f1ca534b62978c6a8e"},"headline":"Research on the principle and application of UV monomer inhibitor","datePublished":"2022-03-14T12:55:14+00:00","dateModified":"2024-12-11T15:34:31+00:00","mainEntityOfPage":{"@id":"https:\/\/longchangchemical.com\/research-on-the-principle-and-application-of-uv-monomer-inhibitor\/"},"wordCount":1830,"publisher":{"@id":"https:\/\/longchangchemical.com\/#organization"},"articleSection":["Catalysts & Chemical Auxiliary Agents"],"inLanguage":"hu"},{"@type":"WebPage","@id":"https:\/\/longchangchemical.com\/research-on-the-principle-and-application-of-uv-monomer-inhibitor\/","url":"https:\/\/longchangchemical.com\/research-on-the-principle-and-application-of-uv-monomer-inhibitor\/","name":"Az UV monomer inhibitor elv\u00e9nek \u00e9s alkalmaz\u00e1s\u00e1nak kutat\u00e1sa - 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