DE1495043A1 - Haertbare Epoxyharzmassen - Google Patents
Haertbare EpoxyharzmassenInfo
- Publication number
- DE1495043A1 DE1495043A1 DE19621495043 DE1495043A DE1495043A1 DE 1495043 A1 DE1495043 A1 DE 1495043A1 DE 19621495043 DE19621495043 DE 19621495043 DE 1495043 A DE1495043 A DE 1495043A DE 1495043 A1 DE1495043 A1 DE 1495043A1
- Authority
- DE
- Germany
- Prior art keywords
- alt
- hardenable
- old
- dioarbon
- hen
- 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.)
- Pending
Links
- 239000003822 epoxy resin Substances 0.000 title 1
- 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 title 1
- 229920000647 polyepoxide Polymers 0.000 title 1
- 150000008064 anhydrides Chemical class 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 2
- 241000209202 Bromus secalinus Species 0.000 claims 1
- YNPNZTXNASCQKK-UHFFFAOYSA-N Phenanthrene Natural products C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 claims 1
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 claims 1
- 244000269722 Thea sinensis Species 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- 101150001823 alaA gene Proteins 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241001136792 Alle Species 0.000 description 1
- 229920001342 Bakelite® Polymers 0.000 description 1
- 240000007124 Brassica oleracea Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 241001002724 Latana Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 101100091494 Mus musculus Rorc gene Proteins 0.000 description 1
- CVRALZAYCYJELZ-UHFFFAOYSA-N O-(4-bromo-2,5-dichlorophenyl) O-methyl phenylphosphonothioate Chemical compound C=1C=CC=CC=1P(=S)(OC)OC1=CC(Cl)=C(Br)C=C1Cl CVRALZAYCYJELZ-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 101100208299 Rattus norvegicus Ttr gene Proteins 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 208000000260 Warts Diseases 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000011717 all-trans-retinol Substances 0.000 description 1
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Natural products OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
- 235000019169 all-trans-retinol Nutrition 0.000 description 1
- -1 atav ion Chemical class 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 239000004637 bakelite Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- ZEKANFGSDXODPD-UHFFFAOYSA-N glyphosate-isopropylammonium Chemical compound CC(C)N.OC(=O)CNCP(O)(O)=O ZEKANFGSDXODPD-UHFFFAOYSA-N 0.000 description 1
- 229910000698 pewters Inorganic materials 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 201000010153 skin papilloma Diseases 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
- C08G59/4223—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof aromatic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/54—Preparation of carboxylic acid anhydrides
- C07C51/567—Preparation of carboxylic acid anhydrides by reactions not involving carboxylic acid anhydride groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/30—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings
- C07C57/34—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings containing more than one carboxyl group
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Epoxy Resins (AREA)
- Exhaust Gas After Treatment (AREA)
- Aiming, Guidance, Guns With A Light Source, Armor, Camouflage, And Targets (AREA)
Description
Si· Ezfiodusg botrlXft gowlM· neu· organisch· Anhydride,
die wertvoll· BKrtiaVMdttol Ar £po3grhTg«»B»p »lud,
•owl· η·«· wärashllrtber· Bpeaqrharm/Diaiihydrld-UAeeen, dl·
•leh dojroh höh· WÄx»*TerfoieBneet«np«rBtur*n ausseiohn«n.
sind «la· Kl···· von Uarsen, dl· gewöhn!:
durch Umetsen «Ims £plhaloge*ihy6rin· alt eine» Phenol
odor eine« allpaatlMhen sehrwortigen Alkohol erhalten
werden. Dl··« Box»· sind iaiuroh gekennwiohnet, utß mim
"tpoxj^grapp·« enthalt·*» AIo ein«
909806/0968
dar fiareelaholtea alt Hilf· Tea Katalysatoren ader «la·
Oopelyaerleatlen alt HHXe tob HMrtangsaittola» wie PeIyealnra,
Selyaalden und Anhydxlden ergaalgaher Sfcaran era«gliohoa·
Sie Bpsgyharse haben wegen ihrer
■eehaais9hert eheaiseher und
■eehaais9hert eheaiseher und
Bedetttuag unter dta Kunststofftn trlaoet« Si·
in «mtl—ad·· Usng·» auf dta T«r*eoi0deastea Oebl·-
t«n, btlapl«l«wti·* als trbersueteaeetn, PreOutsscn, SLakaaa·-
Imntaa&eatn· Btndtaitt·! ttor Sehlohtetoff·, Klebstoff· und
fur di· Hsrstellaag tlektriiober Isolleiungea verwendet.
lsi Tlelea dieser Verweadun, sarten werden die Harze erhöhten
feapeiatttrea auscesetst· Leider verlieren aber diese Uarae
ihre bei Siaaerteafieratur oder etwas höherer Teaperatur
auseessloJmeten ligeasehaften bei oder nahe Ihrem Krweiobunge-
Obwohl in vielen fttllea Spezyharsaaseen bei Ziamerteapemtur
ameceaftrtet werden kennen» elad war Irsielane tob harsen
ait Sftiaalen üieeneehartea und lnebeeondere einea hohen
Irweiehuncepunkt die Anwenden* von Warm· «ad HMrtuacaaittela
erforderlieh.
la sind sehan viel· vereehiedene EKrtunf aaittel für Epoxy-
n ^ORIGINAL
909806/0968
tent WkMBt9 ait Atnta ftrtlgt Burst ait aWBllth rtrtthlf
Amm ttftBtthafttn trWltM vtriM« TtB 4m WiAtB Beapt-Uimm
TMi BBrtMgMti.tttla9 «mi AbIbm i»4 4m SBmrBMhgrBffi*
4m Mlthata βίο« Ait lttittrta 4t4Brth Mit· te· Ait
Wl Ihrer ttratni»* unter aitvitflXaig tis«r rtlatlY
gm Hmhm· trftlft «bA mi iImi Mtjthirlttta BtMtB
Bit YtrBftltBlMtfAlf fttttr WMttttUiktlt
Ttr tu**·? StIt tin· Mth SiMBfArIAt tlt BKrtMfMitttl
WkMBt CMtrAMtf «tWl mimmbm «BrAt» ABt Alt letimfMkUtatlltttt
AUttr mtttX Aerth BaOWb Atr TtmttMAS··
Aithtt in Am PtXjrBtrtn M tähtwn ftl/MrM Bit BMh
WMtrwr Wnitftitliktlt tnhnn atttttt LtUtr fiht M Mtr
nur vtBtct TtrfVeWrt tttrtMrtMtlnrt ■ tiMhyArlAtt «mA Alt·
t· BlBA VtBiMItBlMBAIt ttmtr MA htWB tlBMi WW
MBkt» A*h« tU BlM Wl AtB tmlitWiMltt Wl Atr
AM MhItBBt Bit Am Bbtb TtrtiigliM· Btr lethttU 4M
WhM AthMltfMkttt Wm A«rth TtMitthM Att BlMBjArIAB
ABBg tlMI Otaltthtt alt «IBM MffVitAMtttllMAM B(
BMht iWrvMAM MrtB· BtBlt «irt mbv Atr
Att BBrtMgMitttlt trhftht MA ttUt YtrtrigUthtelt Bit 4m
Bar· TtrWtttrt· gltlthBtitig vtrita Mtr Alt AmrM 4m
MhyArlA trB|^ltM BigMtthtftM vltAtr Ttrtthltthttrt·
BAD ORIGINAL
909806/0968
909806/0968
a·«· Anhydrid· der for«·!
-OH-O
Κ«
'χ »
Χ 0 - OH
H"1
«•rln B« M't H* uad it"', dl· fltioli ed«r υ·γ·οβ1·6·β «·1β
k0an«n» W««itretoff«tone oder Alkylreet·, dl· ao ««wfihlt
•lad» dU J«d*r ά·Γ Alkylidenrett· S
R·
K« und - Q -
tldlf Kehl·netoffatom· «nthält, «lad, Ph «in· uneubititultrt·
odtr aubetltnl«n· Ph#nyl«nrupj>·, la d«r et««
μητ···β4· 8iikitltu«at«a AlkyXr««t· alt 1 bi· 6 Kohl#ne%pff-
*t«Maf dl· fXdoh oder Vtreehleden «tin ktfaa*a9 elnd, «loh
aue«rord«ntlioh gut aX· BKrtuafaaltteX für £pojqrh*rM *ig-
«iod b«i noxaalcn Temp«r»tur«a
909806/0968
ttftaali «At alt tea «agaalvtelM VMayaanwa ν·ΗΜ§&l«a uaA
•ifOMi M9*M9h*xm/!AmekjM**9*9··* ait μ!ι!·Αμ·Ι·11·βΑμ
t«»fl«Ma» AW SiMi aata laser Atuatrtuaf Aawa a·!» Um·»
μ ι fi i«immH»t«m MaetiaaaMi· AaltiiMi aaflMi 41·
t«MUn«tMi Ban· ia alUiMiMa au»f«Ml*am«t aa M«1aU·
fIAMtMi9 SiIgMi MUT itiiag· teataaafiiai iMia mkrl«it «at·
aat a««aaali«h· BifMM«aaftMi aaA aaaiMwl«aa#t·
Mi fwaO!ll«lc«l«Mi un4
▼mi Ami iaiMi Al· ·%!§· #«iaal wi«4tit«itWn«a Y«vttai«aemi
iat Am Ia«Bfl*a^l9»(VWUB*19t-Al«Mr%enw;uxMBa7ArU)t
la Ami Yk ma »MaylMurMt Ut9 &· «aA 1" **m—nUtU\mm
aaA M «aA V" M«tajl«jrw»p«a alaA9 «la btMBAtn «lrkaaa··
BftrtwaiMdtt·!· Aaaa Al· MtoprMbaaA· TaxUaAmatt la
A* «aA B" MHkfIfiaffM «laA9 AM /
«la
alaA Ui Τ·υ««βΑ«μ Α·ν m«m Dlttk/AvU· al·
HAHaagMlt%«l flbr IjMyUw ·*«* Ait f·1#«Um ttu»tMMfμ
1·) Ala laiilMt MlMaMi Aa* AakyAiAAiMM· «aA Aar
AAvm l)fAlMylii«af# A» Aav laly—WMMlIIa «al·»
909806/0968
• I*
OB ♦
ο · 8 —ψ
•la·* ifiKfjimpf dta Hum «at·* U14ttng tlaif
htyfwae «bA ilMr ftaitB
• 0 - OB ♦
OB1-OB
-8 - 0 - CSU -QH-
}·) 41· MlMtk*al«aafttiWi
grayp«a d·· ?«lyn*vuit <!·
1·) c«allMt«B
- «ad Bpozy
&· in d·»
katalysiert
' OH ♦ OBg · OB ·
N 9/
- OH9 -
»a ta·***!·* um AaayAiiagyaif· aar v»Uatia*i««a Um-Mttaag
ait iinr taiiaa (lMJqr)-ti«pf· uad «ar aaiaagliaa
itUldttam MkiuaUUna BfivaaylfiayM aaevaiaatt wird du
YaaaMltaia T«a W—aydrU aa Byaayaata aMakafiii« al· «m
faaaaltaia Uw yaatiaatliatgaa tiafaaa* d.h. *l· das ▼•r-
BAD ORIGINAL
909806/0968
hUtnl· tw JüuvAitAftq^TaUBtmiXtaiytq^lYftleBUa, Am la
f«lt«aita al· k/a MMlMMt wlrdt ma···»**·
tea AafcyAiiAAfBlvalMt let Al· Hiiilt«ii|i AaIyArIA9
Oiaaaltmlfalaiit ^atfiimff«a MtBtIt9 la g« B· wlrA W-•tlaatt
IaAM «la· Wkaaat· HMf· ^favyhaia alt ·1μ* a··
kaaat«a Marne· Mlaaftm»· aag«Mtst maA 4tr ϋι·η·Μ§ μ
8aun MJrttMtltvUvt miA9 ·· AaI Al· mtomfcafet· Mm«· ·γ-altt«lt
MfMB mbb« Sa «la MtltkOl Uni· alt fr*·*
aaaa Aar Ol«l«hBBf
O · C - ♦ ΙΟΙ » -C-O-
so' & !a
ttBA Mt«MfM· QBMtMBfM9 MA ·· BBt «ltB §«Mlft9 Alt
«Im gat· HAitmag mbm alt liiw §·ιΐΒ§·νΜ al· Aaa
tlsoh ·ΓΓ·νΑ·Α1«ΒΜ YevMlt&le k/M «ralvlt MfAM
#<■■■■
AaAaraiwal«· mHm abar Hare· Bit tftarlaf aaao Β1ι·β·«ββ*%
•ifealt·«· Mm Im TtiUUtnli Α/Λ g*0I»r let al· 1. HU
Βτ&βΑββ* Uattfet al·· is hlrttauraa Iiiiib, «1· «U
Aan «ad «Um· ad ar aafcrar* Aar β«*·β ABhjrArlA· Aar
*mg Ib mUkm «««·· Atf «μ τ·ιΜΐ«α· m A
«1···· VeAlltal· μτΙμΙμβ 0»·9
«■A I9S «a· iMto»raA«r· tml—hm 1#00 «at 1#β|· Β··μ
■«««a aa AbbjAxIA kennen «war vtiMBlti wtttMit
«at Daa«r dty Htrtva« lUkuMBi la ·1α«β
arU«r«D. 1·ι«β ear aftil«·»
kalt «Β« Α·τ «BtajcvvAratUtA 0rt«n TartitfUaakait
tat la »rBitat· flttealft IpajqrhiiBinita atBf«toaaa«
SI· tetfcBftrtoaf *·· Bars··· «aarrai Ur Ut Battfitall
Tamatamaf arfvlft» «1« aloh am· Aar Brral«ka«f A··
«art·· Aar WlnMT«xfaanmtet«Ba«rmtttr ·ι«1Μ» «vfal
BlAU Wl ata 150 M· ffO#O fttr 10*14 8%undae. T*
vtla · wird ·1β· T«ay«ratttr ▼»« waolg«tan· «twa ITO9O aag
It9 ««A Ib all«· wet bib wird ImI KlnAaltvai
♦mr T«a atwa t0090 flr rtwa fO-t4 StwaAra ·1β Bar· al« «Uwr
oat ORfGINAL
909806/0968
Ι·ν &rfia4tuu[ kO&nen α·μ#·^·Χ1% tMuNUm· iallea
•la y^lyali^lkMiin d·* Hml
IiT
«ort» fh# R9 E't S* eni κ"' dl·
h«b«n9 wittaillf «In
h«b«n9 wittaillf «In
A·· Polyallqflbea··!·· alt lUltleeHar^mliydrld la
•in·· fr*i· oftdlk·!· Vlld«iid«i EatAlyaators uoaetat· id· la* ia ·1ηβ·1η·ιι la ter ?at#nt»ni>tld«ne A 99 290 4mr
•in·· fr*i· oftdlk·!· Vlld«iid«i EatAlyaators uoaetat· id· la* ia ·1ηβ·1η·ιι la ter ?at#nt»ni>tld«ne A 99 290 4mr
Si· Krfiadwag a»Xl Ia H0I4«ai«a afilwai τ·η Β·ΐ·ρ1·1·Β alter
T»rar«thMillet ν·!*·*· teil« «aA froatataneab·» b«alA*a
•iok auf Iu 0«al«a%·
•aitcaataMBajUl«) la IS te&Ua «la·· Ib Bui«·! «aUtli
8AD ORIGINAL
909806/096·
Byaxyharsea (t»«a tat - einea Produkt dar Shell 3>«τ·1·ρ·»Β*
Oarpaxatlant te· ala iltlaalga· Iflehlerhydria/Blaphanol~A-■am
alt eiaea alttieren Kolekulargewlaht «wi sehen 390 und
400 und «in·· Sfae/wart· tob 0,52 let) wurde Wl 10 MLa 80*0
berg «at «11«. DtUaar LOaoBg wurdan 0, H fell· Benajldiaathyl«
aale (O9 02 llal/2pwqrllqulYal«nt) sitgaMtat» uad daa Oealaali
ward« garOart» bi· m alnhaltlleli «ar· Ola Löeun« «ard«
la «in· MtfaalnefotB Ton 18 mx 1,25 aa * 1#25 oa» dl· alt
alaaa BlUkaafaxamaalOauneaaltt·! (Dow Oaralag uc-20) Oberaas·«
«ar» eagaeaan· Ein find· dar farn «urd· alt ein·»
8t*paal a«a Sllaatlo 51-Guasl τ·Γ·οίι1ο···η. Dl· Haraaaaaaii
«ordan a Stunden bat 809Q rorg«httrt«t und 20 Stunden bat
8009O naahgahärtat· SIa Wiawrarfonaneataaparatur daa ao
arbaltaBan gahärtat·» Bar···« »«atlaiat aaaJi ASTM-luthod·
9 €46·5« (0t25 na Svflaktlon) betrog 1849C*
·) Per spoxjvart t"Oxiranwert") ist dia Ansah! Bpa*ygruppen
In K1O g Jtipojgrtuire· 10 diridi^rt du roh den Bpox^werl
•rgltot daa IpajgrftqelTalant· üin fiara alt alaea Epojywert
Ton 0,50 hat alaa ein £poxyäquiT«lent tob 200·
Ia wea«nt liehen naah daa Verfahren tob Beiepiel 1 «arda ein
Spajqrhara alt einer WliaaTarfomingataayaratur tob 1929o
T*rwendun£ tob
21 «4 !eilen PhaBylan-bla»(9-butan-1t2-»dlaar%aBaftiira> •nhidrid)
21 «4 !eilen PhaBylan-bla»(9-butan-1t2-»dlaar%aBaftiira> •nhidrid)
2010 Teilen Syaa 828 .. BAOORiQfNAL
0928 XeUaa
909806/0968
U95043
Xa μμΙμογ 14m sImm «A mmx· Im Bant·! «rfeBltlUfe·
Byexyh*»· la v«rt*llAft«r 1·!·· «1% «M mmi HUrtMM*
Mittels uv BifUiMi e*fcl*t«t mmimm* to m**· BMh iM
▼«rf MM» vm BeU»Ul 1 «attr Twmiim tm
ao90 fdULM MkOlt· BU 9TM (BpMIMH - 0,55)
«l MTMm9 mIavm· ii·
ltfl grtitHtM Immi
Tm:
909806/0968
ttrtuagaalttel i**i«««hl*et& wert·». IkUaea Mitt·! let J*»
«•«a «It τ1·1·η SpeaE/haraea, «1« SpoB 81· (Mptxjwmrt 0,51)
Bleat mrtrtfllan «a« kaia9 «a ee iImo T»ia*ltiil willig
baliaa SotaMlspoakt aealtat9 nr eohwer la da* Bum «la*·*
axfceitat w»rd«fi. Die a· Ia«htelle keime* bla a« aloaa g«ai»»
«advrta ttaaxmtadaa »·γ*·π, dai aaa Um aaiam
«1« Phtaalatmvaaalgriili· a—lathi»
«ι ealaa Vartrl«ll«hkalt alt <aa Baxa am τ·«*·βββηι and a·!·
aas SahMlayuaftt μ aankan· J»ah Pe«n/l«n-ala-(V»etan-1tldlaax%onalai«anh/drld)
kaam la Gaalaeh alt I^MaalUtaiara»
dlaaa/drid ala Blrtungavlttal itlr £poxyhars· Vameniat wari«a9
«a Baxa· a« «naugan· dl· al eh durafe alaa hah«
16f1 Tell· Fh«nyl«B-Bla-(5-butao-192-dl««jrWaaftMraaaJ^dJl4)
«ad 3,5 *·11· PyreeelUtaäur^llAnhydrld «urdan aa alaa«
haaoganan Oaalsoh alt alaaa Kxwfbxmgmponkt raa 55*C» daa
aal 909O fUaif Aalg «lrdt eueaaaea^ejoJsaala·». filaaaa ββ-aiaah
«ar«· a« 10 T«il«a Mpvn 818 augeaetat und analnit« MLa
•la· i^lateaaaa trllb· LOaoiif «rhaltcn war· Dlaaer Slia··
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BAD ORIGINAL
909806/0968
Claims (1)
- • it·1495Θ43«1« «U aai al«ft·Q <· GB -> Gt Vβ·· OHg- Oft, κ·· ft· m4 ä··, AU !!«Uli ei·* •·1» kfcniw» HMwmliffiHi «iwr AUqrXtwt·» ü· «La«, «al J*i*r Uwft· 9 Λ mimBADORfQlNAL 909806/0968tulert· oder substituierte rhtnylengrupp·, la der etwa «•»•nde Substituents Alkylreete Mit 1 bl· € Kohlenetoffatoaen, dl« gleich oder reree ieden «ein können» sind, Ib •oloher Mtnge, da· 4a· Verhältnis der AnhydridäquiTaleate sos Kpoj^K«ttlTftltnt«a weoifieten· 0,6 ι 1 betrügt, enthält.2· Hltrtbejre Horsaa··· naoh Anepruoh 1, dadurch selohnet« deJ el· ?hen<ylen-bie-(5-but»«-1,2-dioarbon»fiujpeanhydrid) enthÄlt·5. Härtbar· Hnrwtaeee naeh Anspruch 1, d*dur«h «ekennselebnet, dafi sie Phen^len-ble-C^-eethjrl-^butRn-i.a-dioarbon-•ttureanhjdrid) enthält.4· Härtbare ümxwmmmm· n»oh ei β ta der AneprUohe 1-5» da-4ur«h gekennaelohnet* d«U ele dta· Härtunesolttel In eoloher Menge «nthält, «al dae Verhältale der Anh^dridftqui-Talente ma tpoxyäq^iiralenten swieohen ItI und 1*25 ti liegt.5· Terfafarea «ur Her·teilung einte gehärteten Eposjharse·, dadareh gekemuMiebnet, daß eine Maaee naoh «ineei der As* •jrüehe 1-4 auf eine Taeperatur awl*«hen 150 und 250*0 erhltit »irt. #SADORfGINAL909806/09686· Verfahren nach "nepruch 5» dadurch gek«nnselehset9 daß die iim*i>e euxinchet etwa 2 otunden auf etwa Bn0Q und daan 20 Hi· 24 Stunden auf etwa 2000G erhitst wird·909806/0968
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US86308A US3272843A (en) | 1961-02-01 | 1961-02-01 | Phenylene-bis |
US499132A US3336260A (en) | 1961-02-01 | 1965-09-13 | Dianhydride curing agent for epoxy resins |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1495043A1 true DE1495043A1 (de) | 1969-02-06 |
Family
ID=26774604
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19621443352 Pending DE1443352A1 (de) | 1961-02-01 | 1962-01-05 | Verfahren zur Herstellung von als Haerter fuer Epoxydharze dienenden Dianhydriden aromatisch substituierter Tetracarbonsaeuren |
DE19621495043 Pending DE1495043A1 (de) | 1961-02-01 | 1962-01-25 | Haertbare Epoxyharzmassen |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19621443352 Pending DE1443352A1 (de) | 1961-02-01 | 1962-01-05 | Verfahren zur Herstellung von als Haerter fuer Epoxydharze dienenden Dianhydriden aromatisch substituierter Tetracarbonsaeuren |
Country Status (7)
Country | Link |
---|---|
US (1) | US3336260A (de) |
BE (1) | BE613374A (de) |
CH (2) | CH421070A (de) |
DE (2) | DE1443352A1 (de) |
GB (1) | GB971731A (de) |
NL (1) | NL274272A (de) |
SE (2) | SE305649B (de) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4263209A (en) * | 1979-07-02 | 1981-04-21 | The Dow Chemical Company | Aromatic dianhydrides |
US5156744A (en) * | 1989-02-14 | 1992-10-20 | Fmc Corporation | Process for inhibiting scale using maleic anhydride polymerized in reactive aromatic hydrocarbons |
WO2020180976A1 (en) * | 2019-03-04 | 2020-09-10 | Sabic Global Technologies B.V. | Curable encapsulant including thermoset epoxy composition |
CN112679704B (zh) * | 2020-12-28 | 2023-12-12 | 浙江创赢新材料有限公司 | 一种潜伏型桥连二酸酐固化剂及其制备方法与应用 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL253053A (de) * | 1959-06-24 |
-
0
- NL NL274272D patent/NL274272A/xx unknown
- BE BE613374D patent/BE613374A/xx unknown
-
1962
- 1962-01-05 DE DE19621443352 patent/DE1443352A1/de active Pending
- 1962-01-23 GB GB2514/62A patent/GB971731A/en not_active Expired
- 1962-01-25 DE DE19621495043 patent/DE1495043A1/de active Pending
- 1962-01-26 SE SE901/62A patent/SE305649B/xx unknown
- 1962-01-26 SE SE12159/63A patent/SE303606B/xx unknown
- 1962-02-01 CH CH123862A patent/CH421070A/de unknown
- 1962-02-01 CH CH879166A patent/CH427268A/de unknown
-
1965
- 1965-09-13 US US499132A patent/US3336260A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
SE305649B (de) | 1968-11-04 |
CH427268A (de) | 1966-12-31 |
GB971731A (en) | 1964-10-07 |
DE1443352A1 (de) | 1968-12-05 |
NL274272A (de) | |
CH421070A (de) | 1966-09-30 |
BE613374A (de) | |
US3336260A (en) | 1967-08-15 |
SE303606B (de) | 1968-09-02 |
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