PL99129B1 - ACRYLIC-VINYL SURFACE PAINT - Google Patents
ACRYLIC-VINYL SURFACE PAINT Download PDFInfo
- Publication number
- PL99129B1 PL99129B1 PL17761975A PL17761975A PL99129B1 PL 99129 B1 PL99129 B1 PL 99129B1 PL 17761975 A PL17761975 A PL 17761975A PL 17761975 A PL17761975 A PL 17761975A PL 99129 B1 PL99129 B1 PL 99129B1
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- PL
- Poland
- Prior art keywords
- vinyl
- acrylic
- copolymer
- paint
- weight
- Prior art date
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- 229920002554 vinyl polymer Polymers 0.000 title claims description 13
- 239000003973 paint Substances 0.000 title description 25
- 229920001577 copolymer Polymers 0.000 claims description 12
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 8
- 239000004925 Acrylic resin Substances 0.000 claims description 7
- 229920000178 Acrylic resin Polymers 0.000 claims description 7
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 7
- -1 isobutyl ester Chemical class 0.000 claims description 6
- 239000011347 resin Substances 0.000 claims description 6
- 229920005989 resin Polymers 0.000 claims description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 229920001169 thermoplastic Polymers 0.000 claims description 3
- 239000004416 thermosoftening plastic Substances 0.000 claims description 3
- 125000005907 alkyl ester group Chemical group 0.000 claims description 2
- 150000002576 ketones Chemical class 0.000 claims description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims 1
- 239000012752 auxiliary agent Substances 0.000 claims 1
- 239000001023 inorganic pigment Substances 0.000 claims 1
- 239000012860 organic pigment Substances 0.000 claims 1
- 239000004014 plasticizer Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 description 16
- 238000001035 drying Methods 0.000 description 9
- 239000000126 substance Substances 0.000 description 6
- 239000000049 pigment Substances 0.000 description 5
- IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 3
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 3
- 229940043265 methyl isobutyl ketone Drugs 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 238000004383 yellowing Methods 0.000 description 3
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 2
- 240000002791 Brassica napus Species 0.000 description 2
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 2
- 239000000787 lecithin Substances 0.000 description 2
- 229940067606 lecithin Drugs 0.000 description 2
- 235000010445 lecithin Nutrition 0.000 description 2
- 150000003904 phospholipids Chemical class 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000004071 soot Substances 0.000 description 2
- 235000010215 titanium dioxide Nutrition 0.000 description 2
- 239000002966 varnish Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- RXDDZPRSFAQJOC-UHFFFAOYSA-N butylbenzene;phthalic acid Chemical compound CCCCC1=CC=CC=C1.OC(=O)C1=CC=CC=C1C(O)=O RXDDZPRSFAQJOC-UHFFFAOYSA-N 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- GQKZRWSUJHVIPE-UHFFFAOYSA-N sec-amyl acetate Natural products CCCC(C)OC(C)=O GQKZRWSUJHVIPE-UHFFFAOYSA-N 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
Description
Przedmiotem wynalazku jest farba nawierzchnio¬ wa oparta na substancji blonotwórczej stanowiacej mieszanine termoplastycznych zywic polimeryza- cyjnych — akrylowej i winylowej.The subject of the invention is a topcoat wa is based on a film-forming substance mixture of thermoplastic resins polymerization tions - acrylic and vinyl.
Farba przeznaczona jest miedzy innymi do osta¬ tecznego malowania nadwodnych czesci /burt, nad¬ budówek, masztów, zzebnic pokryw lukowych/ stat¬ ków zabezpieczenia ich przed niszczacymi wplywa¬ mi atmosferycznymi i nadania calemu zestawowi dodatkowych wlasnosci fizykochemicznych, jak np. twardosc, elastycznosc, przyczepnosc oraz wymaga¬ nych walorów dekoracyjnych, jak kolor, polysk, gladkosc itp.The paint is intended, inter alia, for the last side / side paint finish, over buildings, masts, gears, hatch covers / stats to protect them from the destructive influence weather conditions and give the whole set additional physicochemical properties, such as hardness, flexibility, adhesion and requirements various decorative values, such as color, gloss, smoothness etc.
Dotychczas znane i stosowane farby nawierzch¬ niowe oparte sa na lakierniczych zywicach synte¬ tycznych modyfikowanych olejami roslinnymi da¬ jacych powloki schnace desydatywnie, na tych zy¬ wicach poddanych chemicznej modyfikacji /zywice alkidowe akrylowane, oleje uretanowane/, na zy¬ wicach polimeryzacyjnyeh tworzacych powloki wy¬ sychajace fizycznie /chlorokauczuk, polichlorek wi¬ nylu/ badz tez na spoiwach mieszanych zawieraja¬ cych zywice schnace ofcsydatywnie i fizycznie ./spoi¬ wa aikidowo-chlorokauczukowe/.So far known and used surface paints The new ones are based on varnish synthetic resins modified with vegetable oils any desidatively drying coatings on these veins chemically modified vices / resins acrylated alkyd oils, urethane oils /, ex polymerization vines forming the coatings of the coatings physically drying / chlorinated rubber, polychloride, nylon / or on mixed binders contain resins, which are physically and chemically drying wa aikidowo-chlorokauczukowe /.
Spoiwa na bazie 'mieszanin zywicy akrylowej i winylowa uzyte do farb nawierzchniowych stoso¬ wane sa w dziedzinie wyrobów dyspersyjnych i wy¬ palanych.Binders based on mixtures of acrylic resin and vinyl used as topcoat paints are important in the field of dispersion products and smoked.
Zywice akrylowe sa w tych przypadkach typu wodorozcienczalnego lub termoutwardzalnego, a zy- 80 wice winylowe stanowia najczesciej octany poliwi¬ nylu, kopolimery chlorku winylu, chlorku winili- denu i fluorku winylu. Opisy patentowe St. Zjedn.Acrylic resins are in these cases of the type water-soluble or thermosetting, and 80 The vinyl vices are most often polyvinyl acetates vinyl chloride, vinyl chloride copolymers, dene and vinyl fluoride. U.S. patents US
Am. 3 305 602, 3 231393, W. Brytanii 1361493 i Czechoslowacji 160 873.Am. 3,305,602, 3,231,393, Great Britain 1,361,493 i Czechoslovakia 160 873.
Powloki wymienionych farb nawierzchniowych nie spelniaja wszystkich wymaganych przez uzyt¬ kowników warunków, a to z uwagi na dlugie cza¬ sy schniecia, nietrwale w czasie eksploatacji walo¬ ry dekoracyjne, a takze ze wzgledu na niepozada¬ ne efekty powierzchniowe w czasie nakladania farb walkiem lub natryskiem.Coatings of the above-mentioned topcoats do not meet all required by the user conditions, and this is due to the long time The drying system is dry, the roller does not have good durability during operation decorative rice, as well as because of the inconvenience low surface effects during paint application by a fight or a spray.
Celem wynalazku jest opracowanie farby na¬ wierzchniowej która tworzy powloki odznaczajace sie szybkim wysychaniem oraz wysokimi walorami dekoracyjnymi, jak polysk i czystosc barwy, przy dlugotrwalym ich zachowaniu na poziomie wyjscio¬ wym, a takze tworzy powloki charakteryzujace sie dobra przyczepnoscia do powlok farb sporzadzanych na bazie róznorodnych substancji blonotwórczych; nadaje sie zatem jako ostatnie wymalowanie na ze¬ stawy gruntowych i podkladowych farb chlorokau- czukowych i poliwinylowych, a równiez do reno¬ wacji powlok alkidowych.The object of the invention is to develop a paint for use with outer surface which creates distinctive coatings with fast drying and high values decorative, such as gloss and purity of color, with their long-term behavior at the exit level and also creates coatings that are characterized by good adhesion to paints prepared based on various cellulose substances; it is therefore suitable as the last paint in the dark ponds of ground and base chlorinated paints tungsten and polyvinyl as well as for renna alkyd coatings.
Cel wynalazku zostal osiagniety przez sporzadze¬ nie szybkóschnacej farby nawierzchniowej akrylo- wo winylowej, która przez okres conajmniej jedno¬ rocznej eksploatacji zapewnia estetyczny dekoracyj¬ ny wyglad wymalowan na obiektach takich jak nadwodne czesci statków oraz, której zastosowanie 99 12999129 3 - zmniejsza naklady na prace konserwacyjno-malar- skie.The object of the invention has been achieved by the preparation non-fast-drying acrylic topcoat of vinyl, which for a period of at least one annual use provides an aesthetic decoration new appearance painted on objects such as above-water parts of ships and the use of which 99 12999129 3 - reduces expenditure on maintenance and painting skie.
Farba nawierzchniowa wedlug wynalazku oparta jest na mieszaninie termoplastycznej zywicy akry¬ lowej stanowiacej kopolimer alkilowych estrów kwasu akrylowego i metakrylowego lub kopolimer Winylotoluenu z estrem izobutylowym kwasu me¬ takrylowego o wartosci K w granicach 35—45 z zywica winylowa stanowiaca kopolimer chlorku wi¬ nylu zawierajacy 83—85°/o chlorku winylu oraz wolne grupy wodorotlenowe w ilosci do 2°/o wago¬ wych i charakteryzujacy sie wartoscia K rzedu 40 ± 2, przy czym stosunek wagowy zywicy akry¬ lowej do winylowej jest jak 3—3,5 do 1—1,5 ko¬ rzystnie 3,2 : 1.The topcoat according to the invention is based it is on a thermoplastic acrylic resin mixture a copolymer of alkyl esters acrylic and methacrylic acid or copolymer Vinyl toluene with isobutyl ester of meta acid tacrylate with a K value in the range of 35-45 z vinyl resin which is a copolymer of chloride nylon containing 83-85% of vinyl chloride and free hydroxyl groups up to 2% by weight and characterized by the value of K row 40 ± 2, the weight ratio of acrylic resin for vinyl to vinyl is from 3-3.5 to 1-1.5% Preferably 3.2: 1.
Oparcie skladu farby na substancji blonotwórczej stanowiacej termoplastyczna zywice akrylowa — kopolimer alkilowych estrów kwasu akrylowego i metakrylowego lub winylotoluenu z estrem izobu¬ tylowym kwasu metakrylowego o wartosci K w granicach 35—45 zapewnia otrzymanie powlok o wysokich walorach dekoracyjnych, dlugotrwalych dzieki ich duzej odpornosci na degradujace dziala¬ nie czynników atmosferycznych i chemicznych.Basing the paint composition on a film-forming substance constituting a thermoplastic acrylic resin - alkyl ester copolymer of acrylic acid i methacrylic or vinyl toluene with an isobium ester methacrylic acid with the value of K w limits 35-45 ensures that the coatings are obtained high decorative and long-lasting values thanks to their high resistance to degrading effects no atmospheric and chemical factors.
Modyfikacja zywica winylowa — kopolimerem chlorku winylu z wolnymi grupami wodorotleno¬ wymi zwieksza elastycznosc i twardosc powlok, a przede wszystkim nadaje im wybitna przyczepnosc do powlok farb sporzadzonych na bazie substancji blonotwórczych innego typu, stwarzajac mozliwosc szerokiego zakresu stosowania farby wedlug wy¬ nalazku. niska retencje rozpuszczalnika w powloce oraz wlasnosci Teologiczne zmniejszajace ryzyko tworze¬ nia sie w czasie aplikacji farby takich wad powlo¬ ki, jak pecherzykowanie i kraterkowanie.Modification of vinyl resin - copolymer vinyl chloride with free hydroxyl groups Due to its properties, it increases the flexibility and hardness of the coatings, a above all, it gives them outstanding grip for substance-based paint coatings other types of film forming, creating an opportunity wide range of paint application according to the exclusion invention. low solvent retention in the coating and Theological properties that reduce the risk of creation during the application of the paint, such defects appear ki, such as bubble and crater.
Farba nawierzchniowa wedlug wynalazku jest plastyfikowana monomerowym zmiekczaczem — ftalanem butylobenzylowym w ilosci okolo 20°/o wagowych liczac na sucha substancje blonotwór- cza. W sklad czesci pigmentowej wchodza pigmen¬ ty organiczne i nieorganiczne powszechnie stoso¬ wane do farb tego rodzaju, z wykluczeniem bieli cynkowej w przypadku kolorów jasnych. Dodatek niewielkiej ilosci — okolo 0,1% na gotowy wyrób srodka tiksotropujacego stanowiacego, pochodna o- leju rycynowego nadaje farbie konsystencje lekko tiksotropowa, dzieki czemu unika sie tworzenia za¬ cieków w przypadku nakladania grubszych warstw farby na powierzchnie pionowe.The topcoat according to the invention is plasticized with monomer softener - 20% of butylbenzyl phthalate by weight, counting on the dry film forming substances cza. The pigment part consists of a pigment organic and inorganic compounds are commonly used suitable for paints of this kind, except white zinc in the case of light colors. Addition a small amount - about 0.1% for the finished product a thixotroping agent which is a derivative of The castor funnel gives the paint a light texture thixotropic, thus avoiding compound formation watercourses in case of thicker layers paints for vertical surfaces.
Wprowadzenie do skladu farby dodatku lecytyny sojowej lub rzepakowej w ilosci 1—l,5°/o wagowych liczac na zawartosc pigmentu, ulatwia jego zwil¬ zanie i ucieranie co jest szczególnie korzystne w przypadku rozdrabniania pigmentów takich jak np. blekit paryski czy sadza.Lecithin additive is introduced into the paint composition of soybean or rapeseed in an amount of 1-5% by weight counting on the pigment content, facilitates its moistening rubbing and grinding which is especially advantageous in in the case of grinding pigments such as e.g. Paris blue or soot.
Z zestawienia widac, ze powloka farby nawierzch¬ niowej akrylowo-winylowej wedlug wynalazku, po¬ siada najkrótszy czas schniecia i w porównaniu do powloki farb dotychczas stosowanych wykazuje najlepsze wlasnosci — zachowujac po uplywie 6-cio miesiecznej ekspozycji w stacji badan terenowych wyjsciowe walory dekoracyjne, jak polysk i ko¬ lor.The list shows that the surface paint coating acryl / vinyl vinyl according to the invention, the shortest drying time and compared to the coating of paints used so far shows best properties - keeping after 6th monthly exposure at the field research station original decorative qualities such as gloss and color lor.
Tablica Nazwa wyrobu wlasnosci powlok Schniecie powloki (pylosuchosc) Polysk po uplywie 6-cio mies. ekspozycji miesza- 1 niny wg BN-67/6110-20 Zmiana barwy po 6-cio J mies. ekspozycji Kredowanie po 6-cio 1 mies. ekspozycji | Farba na¬ wierzchniowa chlorokauczuko- I wa 1 godz. 44 silne zzólkniecie wysoki stopien zatrzymania bru¬ du silne Farba na¬ wierzchniowa winylowo-alki- dowa 0,5 godz. 70 lekkie zzólknie¬ cie sredni sto¬ pien zatrzyma¬ nia brudu srednie Farba na¬ wierzchniowa ftalowa 12 godz. 64 lekkie zzólknie¬ cie sredni sto¬ pien zatrzyma¬ nia brudu silne Farba na¬ wierzchniowa akrylowo-winy- lowa min. 88 bez zmian nie 1 zatrzymuje brudu nie wystepuje Odpowiedni dobór skladu rozpuszczalników sta- Przyklad I nowiacy mieszanine estrów, ketonu i weglowodoru aromatycznego, w proporcji octanu butylu 20—30% ^ wagowych, octanu etyloglikolu 25—35*/o wagowych, metyloizobutyloketonu 20—2Wo wagowych i ksy¬ lenu 15—25*/o wagowych zapewnia farbie dobra rozlewnosc, krótki czas schniecia powlok, wymaga¬ na temperature zaplonu wyrobu, powyzej 2l°G, ^ czesci wagowych Kopolimer akrylanu etylu i metakryla- nu o wartosci K 35—45 — 18,0 Kopolimer chlorku winylu i akrylanu 2-hydróksypropylowego o zawartosci wolnych grup wodorotlenowych do 2?l%99 129 wagowych i wartosci K rzedu 40 ± 2 Ftalan butylobenzylowy o wsp. zal. sw. 1,532 ± 0,002 Biel tytanowa /Rutil/ Uwodorniony olej rycynowy o temp. topn. 120—135°C Octan butylu Octan etyloglikolu Metyloizobutyloketon Ksylen Przyklad II — 5,4 — 4,5 — 20,0 — 0,1 — 14,0 — 16,0 — 12,0 — 10,0 100,0 czesci wagowych Kopolimer winylotoluenu z metakryla- nem izobutylu o wartosci K 35—45 — 18,8 Kopolimer chlorku winylu, octanu wi¬ nylu i alkoholu winylowego o zawar¬ tosci wolnych grup wodorotlenowych do 2°/o wagowych i wartosci K rzedu 40 ± 2 — 5,8 Ftalan butylobenzynowy o wsp. zal. sw. 1,532 ± 0,002 — 4,5 Biel tytanowa /Rutil/ — 18,0 Zólcien pigmentowa 10G — 0,4 Sadza lakowa — 0,2 Uwodorniony olej rycynowy o temp. top. 120—135°C — 0,1 Lecytyna rzepakowa stanowiaca mie- 6 szanine fosfolipidów z olejem macierzy¬ stym o zawartosci fosfolipidów powyzej 65% — 0,2 Octanbutylu — 14,0 Octan etyloglikolu — 16,0 Metyloizobutyloketon — 12,0 Ksylen — 10,0 100,0Blackboard product name ownership of the coatings Coating drying (dustiness) Gloss after 6th monthly exposure mixed 1 nina according to BN-67 / 6110-20 Color change after the 6th J month of exposure Chalking for 6 1 month of exposure | Paint on¬ outerwear chlorinated rubber And wa 1 hour 44 severe yellowing high degree arrest bru¬ du strong Paint on¬ outerwear vinyl-alcohol- dowa 0.5 hours 70 slight yellowing average table the money stopped dirt medium Paint on¬ outerwear phthalic 12 h 64 slight yellowing average table the money stopped dirt strong Paint on¬ outerwear acrylic-fault- low min. 88 no change no 1 stops dirt absent A suitable selection of the composition of the solvents is Example I brand new mixture of esters, ketone and hydrocarbon aromatic in the proportion of butyl acetate 20-30% by weight of ethyl glycol acetate 25-35% by weight, methyl isobutyl ketone 20-2 by weight and xy 15-25% by weight of flax provides a good paint flow, short drying time of the coatings, required to the ignition temperature of the product, above 2l ° G, ^ parts by weight Ethyl acrylate and methacrylate copolymer nu with a value of K 35-45 - 18.0 Vinyl chloride and acrylate copolymer 2-Hydroxypropyl content free hydroxyl groups up to 2 µl% 99 129 weight and K values in the order of 40 ± 2 Butylbenzyl phthalate with an imp. St. 1.532 ± 0.002 Titanium white / Rutil / Hydrogenated castor oil with a temperature of top 120-135 ° C Butyl acetate Ethylglycol acetate Methyl isobutyl ketone Xylene Example II - 5.4 - 4.5 - 20.0 - 0.1 - 14.0 - 16.0 - 12.0 - 10.0 100.0 parts by weight Vinyltoluene copolymer with methacrylate- isobutyl with a K value of 35-45 - 18.8 Copolymer of vinyl chloride, vinyl acetate of nylon and vinyl alcohol with the content of the amount of free hydroxyl groups to 2% by weight and K values of 40 ± 2 - 5.8 Butylbenzene phthalate with an imp. St. 1.532 ± 0.002 - 4.5 Titanium white / Rutil / - 18.0 Pigment yellow 10G - 0.4 Varnish soot - 0.2 Hydrogenated castor oil with a temperature of top. 120-135 ° C - 0.1 Rapeseed lecithin, which is 6 shaltons of phospholipids with mother oil stimulant with a phospholipid content above 65% - 0.2 Butyl acetate - 14.0 Ethylglycol acetate - 16.0 Methylisobutyl ketone - 12.0 Xylene - 10.0 100.0
Claims (1)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL17761975A PL99129B1 (en) | 1975-01-28 | 1975-01-28 | ACRYLIC-VINYL SURFACE PAINT |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL17761975A PL99129B1 (en) | 1975-01-28 | 1975-01-28 | ACRYLIC-VINYL SURFACE PAINT |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL99129B1 true PL99129B1 (en) | 1978-06-30 |
Family
ID=19970730
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL17761975A PL99129B1 (en) | 1975-01-28 | 1975-01-28 | ACRYLIC-VINYL SURFACE PAINT |
Country Status (1)
| Country | Link |
|---|---|
| PL (1) | PL99129B1 (en) |
-
1975
- 1975-01-28 PL PL17761975A patent/PL99129B1/en unknown
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