NO743651L - - Google Patents

Info

Publication number
NO743651L
NO743651L NO743651A NO743651A NO743651L NO 743651 L NO743651 L NO 743651L NO 743651 A NO743651 A NO 743651A NO 743651 A NO743651 A NO 743651A NO 743651 L NO743651 L NO 743651L
Authority
NO
Norway
Prior art keywords
mol
weight
coating
heat
esters
Prior art date
Application number
NO743651A
Other languages
Norwegian (no)
Inventor
W Schmalz
W Michel
M Schoen
Original Assignee
Cassella Farbwerke Mainkur Ag
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Cassella Farbwerke Mainkur Ag filed Critical Cassella Farbwerke Mainkur Ag
Publication of NO743651L publication Critical patent/NO743651L/no

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04Polyurethanes
    • C09D175/06Polyurethanes from polyesters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/42Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4205Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups
    • C08G18/4208Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/80Masked polyisocyanates
    • C08G18/8061Masked polyisocyanates masked with compounds having only one group containing active hydrogen
    • C08G18/807Masked polyisocyanates masked with compounds having only one group containing active hydrogen with nitrogen containing compounds
    • C08G18/8074Lactams

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Paints Or Removers (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Polyurethanes Or Polyureas (AREA)

Description

I varme herdbare overtrekksmidler In heat curable coatings

til sméltebelegning. for melt coating.

Gjenstanden for påtent nr* ....... (patentsøknad nr. 3240/72) er i varme herdbare pjilfiverformede overtrekksmidler av et bindemiddel bestående av en;hydroksylgruppeholdig polyester og et ;maskert polyisocyahat og eventuelt ytterligere vanlige tilsetninger. ;Disse overtrekksmidler erkarakterisert vedat bindemidlet består av A) til 30 til 45 vekt? av en polyester av en gjennomsnittlig molekylvekt fra. 500 til 6000, et syretall under 20, et OH-tall fra 400 til 800 og et mykningspunkt fra 80 til 150°C, fremstillet av en blanding, ;I) av 90 til 10 mol% isoftalsyre eller dens estere og 10 til 90 mol>S tereftalsyre eller dens estere og II) en blanding av 70 til 100 mol? av en eller fleire mettede alifatiske polyoler méd 4 til 6 OH-grupper med 30 til 0 molSS av en eller fiere alifatisk mettede glykoler, hvis hydroksylgrupper er adskilt fra hverandre med minst 3 C-atomer og B) til 55 til 70 vekt? av et di- eller polyisocyanat, hvis isocyanatgruppe helt eiler delvis er maskert med et i varme igjen avspaltbart laktam og ;fl). inntil. 2 vekt$ av en aksellerator. ;Etter den lære aom fremgår av overnevnte patent påføres dette overtrekksmiddel som vanlig i pulverform på overflaten som ;skal beskytte^^,f.eks. ved påstøvnihg eller elektrostatisk påsprøyt-ning og overtrekket frembringes ved oppvarmning. Innbrenningstempera-turene ligger ved 150 og 250°C, fortrinnsvis 180 til 200°C, inn-brenriingstidene ligger ved 10 til 60 minutter, fortrinnsvis ved 20 til 40 minutter. ;Det er nå blitt funnet at de samme i varme herdbare;J overtrekksmidler er fremragende egnet til påføring fra smelte* På-føringen fra smelte foregår oppløsningsmiddelfritt ved temperaturer mellom; 80 og 140°C, fortrinnsvis mellom 100 og 120°C etter de hertil vanlige metoder, spesielt ved vaising eller rakling. Deretter ut-herdnes det påførte overtrekksmiddel ved ten^eraturer ovér 150°C til hårde, elastiske, klimafaste overtrekk. > Arbeidsmåten å påføre belegg fra smelte istedenfor fra. oppløsninger i organiske oppløsningsmidler er kjent under anvendelse av termoplastiske kunststoffer. LiléLedes hører smelte-klebere, dvs. termoplaster som påføres i smeltet tilstand som klebe-stoff til teknikkens stand. Én anvendelse av slike termoplaster til belegg av metalliske underlag istedenfor en innbrenningslakkering fører ikke til-hårde og motstandsdyktige overflater, deres skraper-følsomhet er så sfeor at klimabestandigheten ikke er tilstede i Ønsket grad. • Ved forsøk, på istedenfor termoplastene å anvende varme-herdende bindemidler, slik det er vanlig i innbrenningslakker for industriell lakkering, viser det seg at de oppløsningsfrie i smelte-strøm ved de til anvendelse kommende temperaturer allerede, delvis gelédanner etter minutter. Dessuten ligger smeltens viskositet allerede ved begynnelsen så høyt at en påføring ved vaising eller The object of claim no* ....... (patent application no. 3240/72) is in hot curable pjilfiver-shaped coverings of a binder consisting of a polyester containing a hydroxyl group and a masked polyisocyanate and possibly further common additives. These coating agents are characterized in that the binder consists of A) to 30 to 45 weight? of a polyester of an average molecular weight from. 500 to 6000, an acid number below 20, an OH number from 400 to 800 and a softening point from 80 to 150°C, prepared from a mixture, ;I) of 90 to 10 mol% of isophthalic acid or its esters and 10 to 90 mol >S terephthalic acid or its esters and II) a mixture of 70 to 100 mol? of one or more saturated aliphatic polyols with 4 to 6 OH groups with 30 to 0 molSS of one or more aliphatic saturated glycols, whose hydroxyl groups are separated from each other by at least 3 C atoms and B) to 55 to 70 weight? of a di- or polyisocyanate, whose isocyanate group is completely or partially masked with a heat-releasable lactam and ;fl). up to. 2 weight$ of an accelerator. According to the teaching aom appears from the above-mentioned patent, this coating agent is applied as usual in powder form to the surface which is to protect^^, e.g. by dusting or electrostatic spraying and the coating is produced by heating. The firing temperatures are at 150 and 250°C, preferably 180 to 200°C, the firing times are at 10 to 60 minutes, preferably at 20 to 40 minutes. ;It has now been found that the same in heat curable;J coating agents are excellently suitable for application from the melt* The application from the melt takes place solvent-free at temperatures between; 80 and 140°C, preferably between 100 and 120°C according to the usual methods for this purpose, especially by vaising or rakling. The applied coating agent is then cured at temperatures above 150°C into hard, elastic, climate-resistant coatings. > The method of applying coating from melt instead of from. solutions in organic solvents are known using thermoplastic plastics. LiléLedes belongs to the state of the art in hot-melt adhesives, i.e. thermoplastics that are applied in a molten state as an adhesive. One application of such thermoplastics for coating metallic substrates instead of a burn-in coating does not lead to hard and resistant surfaces, their scratch sensitivity is so great that the climate resistance is not present to the desired degree. • When trying to use heat-setting binders instead of the thermoplastics, as is common in burn-in varnishes for industrial painting, it turns out that the solvent-free in the melt flow at the temperatures to be used already partially gel after minutes. Moreover, the viscosity of the melt is already so high at the start that an application by vaising or

-' rakling ikke er mulig.-' Rakling is not possible.

Det var derfor overraskende at de i overnevnte patent omtalte pulverlakker er således fremragende egnede midler til smelte- belegg. Eksempel 1. It was therefore surprising that the powder coatings mentioned in the above-mentioned patent are thus excellently suitable agents for hot-melt coating. Example 1.

En etter forskriftene i DOS 2.146.841, eksempel 4, fremstilte overtrekksmiddel oppvarmes ved 120°C og smeltes herved under omrøring og påføres i flytende tilstand med en filmtrekke-trekant resp. en lakkhantel på elektrolyttisk fortynnet blikk slik det vanligvis forarbeides i blikkemballasjeindustrien. Ved en spaltebredde på 25/U innstilles avtrekningshastigheten således at det.fremkommer en filmtykkelse på lO^u. Etter innbrenning i 15 min- . utter ved 180°C får man et meget godt forløpende glatt farveløst overtrekk som har følgende egenskaper: Erichsenverdi (DIM 53 156): Blikket revner før lakk-overtrekket. A coating agent produced according to the regulations in DOS 2,146,841, example 4, is heated at 120°C and thereby melted while stirring and applied in a liquid state with a film coating triangle resp. a lacquer dumbbell on electrolytically diluted tin as it is usually processed in the tin packaging industry. With a gap width of 25 µm, the pull-off speed is set so that a film thickness of 10 µm is produced. After burning in for 15 min- . otter at 180°C gives a very well-flowing, smooth, colorless coating which has the following properties: Erichsenverdi (DIM 53 156): The tin cracks before the varnish coating.

Bendeprøve (ECCA-norm; 0,3 mm blikk): T 0. Bending test (ECCA standard; 0.3 mm tin): T 0.

Sterilisasjonsprøve (1 time 121°C varm vanndamp):Sterilization test (1 hour 121°C hot steam):

I orden. Eksempel 2. , All right. Example 2. ,

Det i eksempel 1 anvendte overtrekksmiddel pigmenteresThe coating agent used in example 1 is pigmented

i smeltestrøm ved 120°C ved tilsetning av 35 vekt? titandioksyd (en etter kloridfremgangsmåten fremstillet rutiltype under handelsbe-tegneisen "Kronos titandioksyd Cl 220") under en dissover og påføres deretter som omtalt i eksempel 1 på elektrolytisk fortynnet blikk, in melt flow at 120°C when adding 35 wt? titanium dioxide (a rutile type produced by the chloride method under the trade name "Kronos titanium dioxide Cl 220") under a dissover and then applied as described in example 1 to electrolytically diluted tin,

idet en spåltbredde på 5OyU velges påføringshastigheten således at with a slot width of 5OyU, the application speed is chosen so that

det oppnås en belegning på ca. 50 g pr..blikkplate av 840 mm x 680 mm. Etter innbrenningen ved 180°C i 15, minutter får man en høyglinsende, brilliant forløpende hvit dekklakkering, som har samme egenskaper som omtalt i eksempel 1. Glansgraden ifølge Lange målt med 45° a coating of approx. 50 g per tin plate of 840 mm x 680 mm. After firing at 180°C for 15 minutes, a high-gloss, brilliant continuous white topcoat is obtained, which has the same properties as described in example 1. The degree of gloss according to Lange measured with 45°

optikk, ligger ved 123?. Lakkeringen kan stanses, trykkes, og over-; lakkeres samt kan brettes. optics, located at 123?. The varnishing can be punched, pressed, and over-; can be painted and can be folded.

Eksempel 3» Det i eksempel 2 omtalte pigmenterte overtrekksmiddel haes ved 120°C i oppsmeltet tilstand.på en med damp ved 120°C opp-varmet belegger og på den ved coilbelegg vanlig måte påføres fra coil avløpende blikkbånd (stålblikk av 0,5 mm tykkelse),. En ved en båndhastighet på 16 m/pinutt på beleggeren påført film av 25/U tykkelse viser etter innbrenning ved 300°C i løpet av 85 sekunder et uklanderlig forløp av høyglans og har følgende egenskaper: Example 3 » The pigmented coating agent referred to in example 2 is applied at 120°C in a molten state to a coating heated with steam at 120°C and applied to it in the usual way for coil coating with a strip of tin flowing from the coil (steel sheet of 0.5 mm thickness),. A film of 25/U thickness applied to the coater at a belt speed of 16 m/pinnut shows, after baking at 300°C for 85 seconds, an impeccable course of high gloss and has the following properties:

Erichsenverdi (DIN 53 156): 8,7 mm. >..Irmtrykningshårdhet (DIN 53 153): 115., Erichsen value (DIN 53 156): 8.7 mm. >..Indentation hardness (DIN 53 153): 115.,

Glånsgrad ifølge Lange (45°-optikk): 112$. Gloss level according to Lange (45° optics): $112.

Bendeprøve: Tl. Lakkeringens klimabestandighet ble målt i Atlas Weathero-meter med kullysbuer og.er praktisk talt lik med denne for en handelsyaniig automobildekklakk på basis av alkyd^melaminharpiks. Bending test: Tl. The climate resistance of the paintwork was measured in an Atlas Weatherometer with carbon arcs and is practically equal to that of a commercial automotive topcoat based on alkyd-melamine resin.

Claims (2)

1. Anvendelse av et i varme herdbart overtrekksmiddel fra et bindemiddel bestående av en hydroksylgruppehoidig polyester og et maskert polyisocyanat og eventuelt ytterligere vanlige tilsetninger, idet bindemidlet består av A) til 30 til 45 vekt? av én polyester med gjennomsnittlig molekylvekt fra 500 til 6000, et syretall under 20, et OH-tall fra 400 til 800b g ét mykningstemperatur fra 80 til 150°C, fremstillet fra en blanding I) av 90 til 10 mol? isoftalsyre eller deres estere og 10 til 90 mol? tereftalsyré eller dens estere og II) en blanding av 70 til 100 mol? av en eller flere mettede alifatiske polyoler med 4. til 6 OH-grupper "■" méd 30 til 0 mol? av én eller flere alif atiske mettede glykoler, hvis hydroksylgrupper er adskilt fra hverandre med .minst- 3,C-atqmer og B) til 55 til 70 vekt? av et di- eller polyisocyanat, hvis isocyanatgruppe helt eller delvis er maskert med.i varme igjen avspaltbart laktam.og C) inntil 2 vekt? av en aksellerator og eventuelt ytterligere vanlige tilsetninger,, fremstilling av varmeherdbare overtrekk ved påføring i smeltet tilstand og etterfølgende utherdning ved innbrenning.1. Use of a heat-curable coating agent from a binder consisting of a hydroxyl group-containing polyester and a masked polyisocyanate and possibly further common additives, the binder consisting of A) to 30 to 45 weight? of one polyester with average molecular weight from 500 to 6000, an acid number below 20, an OH number from 400 to 800b g a softening temperature from 80 to 150°C, prepared from a mixture I) of 90 to 10 mol? isophthalic acid or their esters and 10 to 90 mol? terephthalic acid or its esters and II) a mixture of 70 to 100 mol? of one or more saturated aliphatic polyols with 4 to 6 OH groups "■" with 30 to 0 mol? of one or more aliphatic saturated glycols, whose hydroxyl groups are separated from each other by .at least 3,C atoms and B) to 55 to 70 weight? of a di- or polyisocyanate, whose isocyanate group is fully or partially masked with heat-releasable lactam, and C) up to 2 weight? of an accelerator and possibly further common additives, production of heat-curable coatings by application in a molten state and subsequent curing by burning in. 2. Ved smeltepåføring oppnådd, innbrente overtrekk under anvendelse av det i krav 1 angitte bindemiddel..2. By melt application achieved, burned-in coating using the binder specified in claim 1..
NO743651A 1973-10-18 1974-10-10 NO743651L (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19732352239 DE2352239A1 (en) 1973-10-18 1973-10-18 HEAT-CURABLE COATING AGENTS FOR ENAMEL COATING

Publications (1)

Publication Number Publication Date
NO743651L true NO743651L (en) 1975-05-12

Family

ID=5895744

Family Applications (1)

Application Number Title Priority Date Filing Date
NO743651A NO743651L (en) 1973-10-18 1974-10-10

Country Status (10)

Country Link
JP (1) JPS5073922A (en)
AT (1) AT328051B (en)
BE (1) BE821200A (en)
DE (1) DE2352239A1 (en)
DK (1) DK530874A (en)
FR (1) FR2248302B2 (en)
GB (1) GB1443292A (en)
NL (1) NL7413347A (en)
NO (1) NO743651L (en)
SE (1) SE7412739L (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2404739C2 (en) * 1974-02-01 1982-04-22 Bayer Ag, 5090 Leverkusen Process for the production of films and coatings
CH677995B5 (en) * 1986-01-31 1992-01-31 Inventa Ag
US4920008A (en) * 1989-03-20 1990-04-24 Eastman Kodak Company Powder coating compositions
BE1008074A3 (en) * 1994-02-14 1996-01-09 Dsm Nv Process for the continuous manner covering a strip-shaped material with a thermosetting paint.

Also Published As

Publication number Publication date
GB1443292A (en) 1976-07-21
DE2352239A1 (en) 1975-04-30
NL7413347A (en) 1975-04-22
FR2248302A2 (en) 1975-05-16
AT328051B (en) 1976-03-10
JPS5073922A (en) 1975-06-18
ATA834674A (en) 1975-05-15
DK530874A (en) 1975-06-16
FR2248302B2 (en) 1978-06-09
SE7412739L (en) 1975-04-21
BE821200A (en) 1975-04-17

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