WO2015034357A1 - Composition de peinture comprenant un complexe polyélectrolyte - Google Patents

Composition de peinture comprenant un complexe polyélectrolyte Download PDF

Info

Publication number
WO2015034357A1
WO2015034357A1 PCT/NL2014/050605 NL2014050605W WO2015034357A1 WO 2015034357 A1 WO2015034357 A1 WO 2015034357A1 NL 2014050605 W NL2014050605 W NL 2014050605W WO 2015034357 A1 WO2015034357 A1 WO 2015034357A1
Authority
WO
WIPO (PCT)
Prior art keywords
polyanion
polycation
poly
pigment
paint
Prior art date
Application number
PCT/NL2014/050605
Other languages
English (en)
Inventor
Wilhelmus Maria Van Der Krieken
Wilhelmus Johannes Antonius MEULEMEESTERS
Christiaan Gerardus Johannes Maria Jans
Original Assignee
Ceradis B.V.
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 Ceradis B.V. filed Critical Ceradis B.V.
Publication of WO2015034357A1 publication Critical patent/WO2015034357A1/fr

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
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/14Paints containing biocides, e.g. fungicides, insecticides or pesticides
    • 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
    • C09D101/00Coating compositions based on cellulose, modified cellulose, or cellulose derivatives
    • C09D101/08Cellulose derivatives
    • C09D101/26Cellulose ethers
    • C09D101/28Alkyl ethers
    • C09D101/286Alkyl ethers substituted with acid radicals
    • 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
    • C09D103/00Coating compositions based on starch, amylose or amylopectin or on their derivatives or degradation products
    • C09D103/04Starch derivatives
    • C09D103/06Esters
    • 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
    • C09D105/00Coating compositions based on polysaccharides or on their derivatives, not provided for in groups C09D101/00 or C09D103/00
    • 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
    • C09D105/00Coating compositions based on polysaccharides or on their derivatives, not provided for in groups C09D101/00 or C09D103/00
    • C09D105/02Dextran; Derivatives thereof
    • 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
    • C09D105/00Coating compositions based on polysaccharides or on their derivatives, not provided for in groups C09D101/00 or C09D103/00
    • C09D105/04Alginic acid; Derivatives thereof
    • 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
    • C09D105/00Coating compositions based on polysaccharides or on their derivatives, not provided for in groups C09D101/00 or C09D103/00
    • C09D105/06Pectin; Derivatives thereof
    • 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
    • C09D105/00Coating compositions based on polysaccharides or on their derivatives, not provided for in groups C09D101/00 or C09D103/00
    • C09D105/08Chitin; Chondroitin sulfate; Hyaluronic acid; Derivatives thereof
    • 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
    • C09D197/00Coating compositions based on lignin-containing materials
    • 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
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/41Organic pigments; Organic dyes
    • 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
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/65Additives macromolecular

Definitions

  • TITLE Paint composition comprising a polyelectrolyte complex FIELD
  • the present invention relates to a paint composition
  • a paint composition comprising a pigment and a polyelectrolyte complex of a polyanion and a polycation, preferably further incorporating an antimicrobial agent.
  • a paint composition typically contains four essential ingredients: carrier liquid, binder, pigment, and additives.
  • Pigments provide the paint with both decorative and protective features. Pigments are solid particles used to provide the paint with various qualities, including but not limited to color, opacity, and durability.
  • the paint may also contain other solid particles such as polyurethane beads. Pigments and other solids add bulk to the paint and their levels are related to the gloss or flatness of the paint.
  • Additives are typically used at relatively low levels in the paint formulation, but contribute to various properties of paints, including rheology, stability, paint performance, and application quality.
  • Antimicrobial agents are additives which work to eliminate microorganisms such as bacteria, algea and fungi.
  • a variety of antimicrobial agents are known and are used for various purposes, Such antimicrobial agents include inorganic agents, for example, those containing metal ions, such as silver, zinc, and copper.
  • inorganic agents for example, those containing metal ions, such as silver, zinc, and copper.
  • organic biocides including organic acids, phenols, alcohols, polyene macrolides, and quaternary ammonium compounds.
  • Paint films can be made fungi- algae- and bacteria-free by incorporating a suitable antimicrobial agent in the paint formulation. Reduction in antimicrobial activity of a paint film is mostly attributed to factors such as degradation of of the antimicrobial agent and dissipation of the antimicrobial agent from paint film due to washing out and/or volatilization from the paint film. The life of a paint film will be enhanced if the antimicrobial agent is retained in the film and on the film surface for a longer period of time.
  • This extended duration of biocidal activity can be achieved by incorporating the antimicrobial agent in a polyelectrolyte complex of a polyanion and a polycation.
  • the invention provides a paint composition comprising a pigment and a
  • polyelectrolyte complex of a polyanion and a polycation.
  • the polyanion and the polycation are present in a relative amount of between 1:2 and 60: 1 (w/w).
  • the polyelectrolyte complex has preferably further incorporated at least one
  • a polyelectrolyte complex of a polyanion and a polycation is an irreversible and insoluble complex.
  • the polyelectrolyte complex has sticky properties and contains polar parts (charged) and apolar parts.
  • the aromatic moieties in the complex may have affinity for pigments and/or for antimicrobial agents. In combination with the sticky character of the polyelectrolyte complex, the pigment and/or antimicrobial agent will be optimally deposited and adhered to a product.
  • said complex having incorporated at least one antimicrobial agent, dramatically improved the protective effect of antimicrobial agents such as chlorothalonil against fungi, in comparison with an antimicrobial agent without said polyelectrolyte complex.
  • said polyelectrolyte complex may provide improved, longer lasting, adherence of the antimicrobial agent to the painted object and/or the adherence to the microbe.
  • the polyanion is preferably selected from the group consisting of a natural polyanion such as xanthan gum, alginate, a lignin compound such as hgnosulfonate, pectin, carrageenan, humate, fulvate, angico gum, gum Kondagogu, sodium alkyl naphtalene sulfonate (Morwet), poly-y-glutamic acid, maleic starch half-ester, carboxymethyl cellulose, chondroitin sulphate, dextran sulphate, hyaluronic acid and a synthetic polyanion such as poly(acrylic acid), polyphosphoric acid, and poly(L-lactide).
  • a most preferred polyanion is a lignin compound such as
  • the polycation is preferably selected from the group consisting of poly-L-lysine, epsilon-poly-L-lysine, poly-L-arginine, poly-allylamine, chitosan oligosaccharide, and chitosan.
  • a most preferred polycation is chitosan.
  • the at least one antimicrobial agent preferably is or comprises a copper salt, zinc pyrithione, a formaldehyde, 3-iodopropargyl-n-butylcarbamate (IPBC), 2-n-octyl-4- isothiazohn-3-one (OIT), 4,5-dichloro-2-(n-octyl)-4-isothiazohn-3-one (DCOIT), carbendazim (CBZ), chlorothalonil (CTL; CAS: 1897-45-6), and/or n-butyl-1,2- benzisothiazolin-3-one, and/or a polyene fungicide such as natamcyin.
  • a most preferred antimicrobial agent is chlorothalonil (CTL; CAS: 1897-45-6).
  • a preferred paint composition according to the invention further comprises a carrier liquid and a binder.
  • the invention additionally provides a method for producing a paint composition comprising a pigment and a polyelectrolyte complex of a polyanion and a polycation, the method comprising a) providing an aqueous solution of a polyanion, wherein the concentration of said polyanion is from 0.1-60 w/v%, b) providing a polycation, c) mixing the polycation with the polyanion solution, thereby forming a precipitate, d) crushing the formed precipitate to form a suspension, and e) adding the suspension to a pigment. It is preferred that at least one antimicrobial agent is added prior to the addition of the suspension to a pigment.
  • the invention further provides a method for producing a painted object, comprising a) applying a composition comprising a pigment and a poly electrolyte complex of a polyanion and a polycation whereby the polyanion and the polycation are present in a relative amount of between 1:2 and 60: 1 (w/w) to a object; and b) drying the applied comprosition, thereby producing a painted object.
  • the invention further provides a use of a paint composition comprising a pigment and a polyelectrolyte complex of a polyanion and a polycation, whereby the polyanion and the polycation are present in a relative amount of between 1:2 and 60: 1 (w/w), for painting of a object.
  • Said paint composition preferably comprises at least one antimicrobial agent.
  • Said use preferably is for preventing, reducing and/or eliminating the presence of pathogenic moulds such as Stachybotrys chartarum.
  • the invention further provides a painted object comprising a pigment and a polyelectrolyte complex of a polyanion and a polycation, whereby the polyanion and the polycation are present in a relative amount of between 1:2 and 60: 1 (w/w).
  • the present invention provides a paint composition
  • a paint composition comprising a pigment and a poly electrolyte complex of a polyanion and a polycation, whereby the polyanion and the polycation are present in a relative amount of between 1:2 and 60: 1 (w/w).
  • Said composition preferably further comprises a carrier liquid, binder, and additives.
  • Each of these ingredients may comprise a single component or several different components that are mixed into the composition.
  • At least one antimicrobial agent is preferably incorporated into the polyelectrolyte complex.
  • polyelectrolyte refers to a molecule consisting of a plurality of charged groups that are linked to a common backbone.
  • polycation is interchangeable with the term "positively charged
  • polyelectrolyte and the term “polyanion” is interchangeable with the term
  • polyelectrolyte complex refers to a complex of oppositely charged polyelectrolytes (a polyanion and a polycation) which form strong electrostatic links, thus avoiding the use of covalent cross-linkers.
  • the complex is not soluble.
  • polycations such as chitosan polymers are positively charged and the cationic amino groups on the glucosamine subunits can interact electrostatically with anionic groups (usually sulfonic acid groups) of poly anions such as lignosulfonate to form polyelectrolyte complexes.
  • Said polyanion is preferably one or more polymers selected from the group
  • a natural polyanion such as xanthan gum, alginate, a lignin compound such as lignosulfonate, pectin, carrageenan, humate, fulvate, angico gum, gum Kondagogu, sodium alkyl naphtalene sulfonate (Morwet), poly-y-glutamic acid, maleic starch half-ester, carboxymethyl cellulose, chondroitin sulphate, dextran sulphate, hyaluronic acid and a synthetic polyanion such as poly(acrylic acid), polyphosphoric acid, and poly(L-lactide).
  • a natural polyanion such as xanthan gum, alginate
  • a lignin compound such as lignosulfonate, pectin, carrageenan, humate, fulvate, angico gum, gum Kondagogu, sodium alkyl naphtalene sulfonate (Morwet)
  • said polyanion is selected from the group consisting of xanthan gum, alginate, humate and lignosulfonate.
  • a most preferred polyanion is or comprises a lignin compound such as lignosulfonate.
  • Said polyanion may comprise two or more distinct polyanions such as, for example, xanthan gum and a lignin compound such as lignosulfonate or pectin and a lignin compound such as lignosulfonate.
  • lignin compound refers to a compound that is derived from naturally occurring lignin or capitan by a process that includes sulphonation. The resulting sulfonic acids are strong acids and lignin compounds are therefore negatively charged at pH values below 7.
  • a preferred lignin compound is selected from Kraft lignin, organosolv lignin and/or lignosulfonate.
  • a Kraft lignin is a polyphenolic product from the Kraft pulping process for the conversion of wood into wood pulp. Included are derivatives from Kraft lignin obtained by oxidation or other chemical modification as is known to the skilled person.
  • organosolv lignin is a polyphenolic product from delignification processes using organic solvents. Included are derivatives from organosolv lignin obtained by oxidation or other chemical modification as is known to the skilled person.
  • Lignosulfonate (also termed lignosulphonate, lignosulfate, lignin sulfonate, ligninsulfonate, ligninsulfonic acid, lignosulfonic acid, lignosulfuric acid, or LST 7) is a water-soluble anionic polymer which is, for example, formed as a by-product in the sulphite pulping process. Lignosulfonates generally have a wide molecular weight distribution, typically in the range of about 500 to about 150,000.
  • Lignosulfonates may comprise different metal or ammonium ions as counter cations of the sulfonate groups such as, for example, copper, zinc, calcium, sodium, potassium, magnesium and aluminium.
  • Suitable examples of lignosulfonates comprise sodium lignosulfonate (e.g. sold as BORRESPERSE NA®, Borregaard LignoTech Ltd, Germany), calcium lignosulfonate (e.g. sold as BORRESPERSE CA®, Borregaard LignoTech Ltd, Germany), ammonium lignosulfonate, potassium lignosulfonate, modified lignosulfonate, derivatives of lignosulfonate, or mixtures thereof. Modified lignosulfonates, and derivatives of lignosulfonates are described in U.S. Patent Nos.: 3639263, 3923532, 4006779, 4017475, 4019995, 4069217,
  • a preferred lignin compound is lignosulfonate.
  • a preferred lignosulfonate is copper, zinc, calcium, sodium, potassium, ammonium, magnesium and/or aluminium lignosulfonate, preferably calcium, sodium, potassium or ammonium lignosulfonate, most preferred calcium lignosulfonate.
  • a most preferred polyanion is a lignin compound such as lignosulfonate, most preferred calcium lignosulfonate.
  • Said polycation is preferably one or more polymers selected from the group consisting of poly-L-lysine, epsilon-poly-L-lysine, poly-L-arginine, poly-allylamine, chitosan oligosaccharide, and chitosan. Most preferably, said polycation comprises or is chitosan.
  • chitosan refers to a linear polysaccharide composed of randomly distributed 6-(l-4)-linked D-glucosamine (deacetylated unit) and N-acetyl- D-glucosamine (acetylated unit). Chitosan is produced by deacetylation of chitin.
  • chitosan relates to chitosan, chitosan derivatives and mixtures of chitosan and chitosan derivatives.
  • chitosan relates to linear p-(l ⁇ 4)-linked glucosamin and N- acetylglucosamin. It may be produced from chitin or its sodium salt (e.g. originating from shrimp) by treatment with aqueous sodium hydroxide at elevated
  • chitin deacetylase EC 3.5.1.41
  • Further sources of chitin are fungi, including Basidiomycetes, Ascomycetes, and Phycomycetes, where it is a component of cell walls and structural membranes of mycelia, stalks, and spores.
  • a most preferred chitosan is from fungi or derived from fungi.
  • deacetylation as determined by colloidal titration is from 50 to 99.9 %, preferably from 70 to 99.8 % and most preferably from 90 to 99.7 %, as compared to chitin.
  • Chitosan derivatives can be prepared by reactions at the amino group (e.g. by N-acylation, formation of N-alkylidene and N-arylidene derivatives, N-alkylation and N-arylation) or at hydroxy groups, as is known to the skilled person.
  • a polyanion for example a lignin compound such as
  • Pigments are solid particles used to provide the paint composition with various qualities, including but not limited to color, opacity, and durability.
  • the paint composition may also contain other solid particles such as polyurethane beads or other solids.
  • pigment refers to both pigments and dyes.
  • Preferred pigments comprise one or more of a nitroso compound, a nitro compound, a monoazo compound, a diazo compound, a stilbene compound, a diarylmethane compound, a triarylmethane compound, a xanthene compound, an acridine compound, a quinoline compound, a methine compound, a thiazole compound, an indamine compound, an indophenol compound, an azine compound, an oxazine compound, a thiazine compound, an aminoketone, an anthraquinone, an indigoid compound, a phthalocyanine, a natural dye, and/or an inorganic pigment, such as titanium dioxide, aluminum silicate, chromium oxide, zirconium oxide and/or manganese oxide.
  • an inorganic pigment such as titanium dioxide, aluminum silicate, chromium oxide, zirconium oxide and/or manganese oxide.
  • Said paint composition preferably comprises between about 0.1 - 60 % (w/w) of one or more pigments, preferably between about 0.5 -50 % (w/w), preferably between about 1 - 40 % (w/w), preferably between about 5 - 30 % (w/w), preferably between about 10-25 % (w/w), preferably between about 20 - 25 % (w/w) of one or more pigments.
  • a preferred composition according to the invention further comprises at least one antimicrobial agent.
  • antimicrobial agent refers to a natural or chemical substance capable of inhibiting and/or eliminating the growth of microorganisms or their spores.
  • Said antimicrobial agent is preferably an antifungal, antibacterial or antialgea compound, or a compound having a broad spectrum of activity against fungi and/or bacteria and/or algeae.
  • a most preferred antimicrobial agent inhibits the growth of algae and fungi such as Stachybotrys chartarum, Cladosporium sphaerospermum, Aspergillus versicolor, Aspergillus glaucus, Penicillium
  • chrysogenum Penicillium aurantiogriseum, Penicillium spinulosum, Penicillium brevicompactum, Chaetomium globosum, Stachybotrys chartarum, Acremonium strictum, Alternaria alternate, Aureobasidium pullulans, Phoma sp and Fusarium species on the surface of the paint after it has been applied.
  • An antimicrobial agent of the present invention preferably is one or more of an inorganic, organometallic and metal-organic or organic antimicrobial agents.
  • inorganic antimicrobial agents include copper salts such as copper oxide, copper thiocyanate, copper bronze, copper carbonate, copper chloride, copper hydroxide (Cu(OH)2 ), copper oxychloride (CuC12 ⁇ 3Cu(OH)2), Bordeaux mixture (CuS04.3Cu(OH)2.3CaS04), copper nickel alloys, and silver salts such as silver chloride or nitrate.
  • copper salts such as copper oxide, copper thiocyanate, copper bronze, copper carbonate, copper chloride, copper hydroxide (Cu(OH)2 ), copper oxychloride (CuC12 ⁇ 3Cu(OH)2), Bordeaux mixture (CuS04.3Cu(OH)2.3CaS04), copper nickel alloys, and silver salts such as silver chloride or nitrate.
  • organometallic and metal-organic antimicrobial agents include zinc pyrithione (the zinc salt of 2-pyridinethiol-l -oxide), copper pyrithione, bis (N- cyclohexyl-diazenium dioxy) copper, zinc ethylene-bis(dithiocarbamate) (i.e. zineb), zinc dimethyl dithiocarbamate (ziram), and manganese ethylene- bis(dithiocarbamate) complexed with zinc salt (i.e. mancozeb).
  • zinc pyrithione the zinc salt of 2-pyridinethiol-l -oxide
  • copper pyrithione bis (N- cyclohexyl-diazenium dioxy) copper
  • zinc ethylene-bis(dithiocarbamate) i.e. zineb
  • zinc dimethyl dithiocarbamate ziram
  • manganese ethylene- bis(dithiocarbamate) complexed with zinc salt i
  • organic antimicrobial agents examples include formaldehyde, , 3-iodopropargyl- n-butylcarbamate (IPBC), 2-n-octyl-4-isothiazolin-3-one (OIT), 4,5-dichloro-2-(n- octyl)-4-isothiazohn-3-one (DCOIT), carbendazim (CBZ), chlorothalonil (CTL; CAS: 1897-45-6), n-butyl-l,2-benzisothiazolin-3-one, dodecylguanidine
  • N-aryl maleimides such as N-(2,4,6-trichlorophenyl) maleimide, 3-(3,4-dichlorophenyl)-l , 1 -dimethylurea (diuron), 2,3,5,6-tetrachloro-4- (methylsulphonyl) pyridine, 2-methylthio-4-butylamino-6-cyclopopylamino-s- triazine, 3-benzo[b]thien-yl-5,6-dihydro-l ,4,2-oxathiazine 4-oxide, 4,5-dichloro-2-(n- octyl)-3(2H)-isothiazolone, 2,4,5,6-tetrachloroisophthalonitrile, tolylfluanid, dichlofluanid, diiodomethyl-p-tosylsulphone, capsciacin, N-cyclopropyl-N
  • alkyldim ethylb enzylamm onium chloride alkyldim ethylb enzylamm onium chloride .
  • polyene fungicide refers to polyene macrolide
  • antimicrobial agent that possess antifungal activity, including natamycin, lucensomycin, filipin, nystatin or amphotericin B, most preferred natamycin.
  • Derivatives of a polyene fungicide such as derivatives of natamycin, are also included.
  • a preferred derivative is a salt or a solvate of a polyene fungicide and/or a modified form of a polyene fungicide such as e.g. differently shaped crystal forms such as the needle-shaped crystal of natamycin described in US7727966.
  • the effective amount of an antimicrobial agent depends on the type of antimicrobial agent and the object to which the antimicrobial agent is added. Thus, the required concentration may differ depending on the efficacy of the individual antimicrobial agent, as is well known to the person skilled in the art. Preferred concentrations are between 1 and 20.000 ppm, more preferred between 50 and 10.000 ppm, most preferred between 500 and 2000 ppm.
  • the at least one antimicrobial agent preferably is or comprises a fungicide, preferably a copper salt, zinc pyrithione, a formaldehyde, 3-iodopropargyl-n- butylcarbamate (IPBC), 2-n-octyl-4-isothiazolin-3-one (OIT), 4,5-dichloro-2-(n-octyl)- 4-isothiazolin-3-one (DCOIT), carbendazim (CBZ), chlorothalonil (CTL; CAS: 1897- 45-6), and/or n-butyl-l,2-benzisothiazolin-3-one.
  • a fungicide preferably a copper salt, zinc pyrithione, a formaldehyde, 3-iodopropargyl-n- butylcarbamate (IPBC), 2-n-octyl-4-isothiazolin-3-one (OIT), 4,5-dichloro-2
  • a paint composition according to the invention preferably further comprises a carrier liquid and a binder.
  • a carrier liquid preferably further comprises a carrier liquid and a binder.
  • Each of such ingredients may comprise a single component or several different components that are mixed into the paint
  • Said carrier liquid is a fluid component of the paint and serves to carry all of the other paint components.
  • the carrier liquid provides the means of "carrying" the pigment and binder in a consistency such that it can be conveniently stored and applied to the surface that is painted.
  • the carrier liquid is part of the wet paint and usually evaporates as the paint forms a film and dries on a surface.
  • Said carrier liquid is usually water in latex paints such as acrylic paints, vinylic paints and polyvinyl acetate paints.
  • the carrier liquid is usually an organic solvent such as linseed oil, petroleum distillate, alcohols, ketones, esters, and/or glycol ethers in oil- based paints such as alkyd paints. The amount and type of liquid is usually determined by features of the other paint components.
  • a binder of a paint composition causes the paint to form a film on and adhere to a surface.
  • the binder comprises a latex resin, usually selected from acrylics, vinyl acrylics, or styrene acrylics.
  • the latex resin particles usually are dispersed in water as the carrier liquid.
  • a binder in an oil-based paint is either natural, synthetic or a combination thereof.
  • a natural binder in an oil-based paint is preferably made from a vegetable oil such as linseed oil, tung oil and soya oil, which oxidizes and hardens upon drying.
  • a synthetic binder in an oil-based paint is preferably based on modified oils called alkyds.
  • Further additives in a paint composition according to the invention comprise defoamers, which break bubbles that are formed in paint during handling, thickeners and rheology modifiers which provide consistency and viscosity and improve the leveling and resistance to spattering, fillers such as calcium carbonate and hydrated magnesium silicate (talc), setting salts such as cobalt octoate, UV stabilizers, and surfactants, which stabilize the paint composition so that the components will not separate.
  • defoamers which break bubbles that are formed in paint during handling
  • thickeners and rheology modifiers which provide consistency and viscosity and improve the leveling and resistance to spattering
  • fillers such as calcium carbonate and hydrated magnesium silicate (talc)
  • setting salts such as cobalt octoate
  • UV stabilizers UV stabilizers
  • surfactants which stabilize the paint composition so that the components will not separate.
  • the invention further provides a method for producing a paint composition comprising a pigment and a polyelectrolyte complex of a polyanion and a polycation, the method comprising a) providing an aqueous solution of a polyanion, wherein the concentration of said polyanion is from 0.1-60 w/v%, preferably 1-50%, preferably about 25%, b) providing a polycation, c) mixing the polycation with the polyanion solution such that the polyanion and the polycation are present in a relative amount of between 1:2 and 60: 1 (w/w), thereby forming a precipitate, d) crushing the formed precipitate to form an suspension, and e) adding the suspension to a pigment.
  • polyanion polyanion
  • polycation poly electrolyte complex
  • pigment are used in a method of the invention as defined herein before.
  • An aqueous solution of a polyanion, such as a lignin compound is preferably prepared by dissolving the polyanion, such as a lignin compound, preferably lignosulfonate, in an aqueous solution, preferably water.
  • An aqueous solution of a polycation, preferably chitosan is preferably prepared by solubilizing the polycation in an aqueous acidic solution comprising an acid such as, for example, lactate, hydrochloric acid, phosphorous acid and/or ascorbic acid.
  • the amount of acid that is required to solubilize the polycation, preferably chitosan depends on the polycation, as is known to the skilled person. For example, for solubilizing chitosan, in general, about 6 ml 37% HC1 is required to obtain a solution of 10 gram chitosan in 1 liter in water.
  • a polycation preferably chitosan
  • an aqueous solution preferably water, for example by gently shaking at 20-23 °C overnight
  • a salt preferably NaCl
  • a polyanion solution preferably a lignosulfonate, xanthan gum, humate, or alginate solution, is preferably added drop wise to the solution comprising a polycation, preferably a chitosan compound.
  • the pH is kept between pH 1 and pH 5.5 by the addition of an acid, preferably hydrochloric acid, lactic acid, ascorbic acid, phosphorous acid, nonanoic acid or acetic acid.
  • the pH is more preferably kept between pH 2.0 and pH 5.0, more preferably between pH 3.0 and pH 4.5 during the formation of a poly electrolyte complex.
  • the temperature is preferably between 0 °C and 100 °C, more preferred between 10 °C and 60 °C, more preferred ambient temperature (15-25 °C).
  • the resulting mixture is preferably stirred during formation of the poly electrolyte complex and the poly electrolyte complex is preferably allowed to settle overnight.
  • a dispersing agent and/or a wetting agent is preferably added and the precipitate is crushed, preferably by milling for example in a bead mill, to provide a suspension comprising the polyelectrolyte complex of a polyanion and a polycation.
  • Said suspension is either generated in an aequeous solution, preferably water, for latex paints such as acrylic paints, vinylic paints and polyvinyl acetate paints, or in an organic solvent such as linseed oil, petroleum distillate, alcohols, ketones, esters, and/or glycol ethers for oil-based paints such as alkyd paints.
  • aequeous solution preferably water
  • latex paints such as acrylic paints, vinylic paints and polyvinyl acetate paints
  • organic solvent such as linseed oil, petroleum distillate, alcohols, ketones, esters, and/or glycol ethers for oil-based paints such as alkyd paints.
  • Said dispersing agent when present, is preferably one or more compounds selected from lignin sulphonate, a carboxyl-containing polymer such as polyacrylate and/or carboxyl-containing polyurethanes, a styrene acrylic polymer, an acrylic co-polymer, polyurethane, an alkylpolysaccharide, salts of aliphatic rosin and naphthenic acid, condensation products of formaldehyde of low molecular weight and naphthene sulfonic acid, higher alkyl sulfate such as sodium lauryl sulfate, alkyl aryl sulfonate such as dodecylbenzene sulfonate, sodium salt or potassium salt of isopropyl benzenesulfonic acid or isopropyl naphthalenesulfonic acid, sulfosuccinates such as sodium dioctyl sulfosuccinate, alkaline
  • Typical dispersing agents are l-(2- aminoethyl)piperazine, 2-amino-6-methoxybenzothiazole, 4-(2-aminoethyl)pyridine, 4-(aminomethyl)pyridine, 3-amino-l,2,4-triazole, l-(3-aminopropyl)imidazole, 4-(2- hydroxyethyl)pyridine and l-(2-hydroxyethyl)imidazole.
  • a disperging agent is preferably present in an amount of between 0 to up to 10% (w/v), more preferred between 0.01 to up to 5 % (w/v), more preferred between 0.02 to up to 1 % (w/v), more preferred about 0.05 % (w/v).
  • Said wetting agent when present, is preferably one or more compounds selected from di-octylsuccinate, polyoxyethylene/polypropylene and tri-stearyl
  • a wetting agent is preferably present in an amount of between 0 to up to 10% (w/v), more preferred between 0.01 to up to 5 % (w/v), more preferred between 0.02 to up to 1 % (w/v), more preferred about 0.05 % (w/v).
  • the relative amount of a polyanion and a polycation that are combined in step c) of a method according to the invention is between 1:2 and 60: 1 (w/w), preferably between 2:1 and 30: 1 (w/w), more preferred between about 5: 1 and about 15: 1 (w/w), even more preferred about 5: 1.
  • the final pH value of the resulting suspension comprising at least one antimicrobial agent may be adjusted to a pH value of between 3-12, more preferred between 4-9, most preferred between pH 5-8.
  • At least one antimicrobial agent is added prior to the addition of the suspension comprising a polyelectrolyte complex to a pigment.
  • Said least one antimicrobial agent is as defined herein above.
  • said polyelectrolyte complex provides improved, longer lasting, adherence of the antimicrobial agent to a painted object and/or adherence to a microbe.
  • a composition comprising a pigment and a polyelectrolyte complex can be provided as a ready-for-use product or as a concentrate.
  • the ready-for-use product may be in the form of an aqueous solution, suspension, aqueous dispersion, oil solution, oil dispersion, or an aerosol preparation.
  • the concentrate can be used, for example, as an additive for coating, or can be diluted prior to use with additional solvents or suspending agents.
  • the invention further provides a method for producing a painted object, comprising a) applying a composition comprising a pigment and a polyelectrolyte complex of a polyanion and a polycation whereby the polyanion and the polycation are present in a relative amount of between 1:2 and 60: 1 (w/w) to a object; and b) drying the applied comprosition, thereby producing a painted object.
  • composition comprising a pigment and a polyelectrolyte complex
  • a pigment and a polyelectrolyte complex can be added directly to a object according to any method known in the art, such as spraying the composition on a object, dipping or immersing a object in the composition, or brushing or rolling the composition onto a object.
  • Said object may be any object composed of any material.
  • Most preferred materials are materials applied in building constructions such as houses and include but are not limited to wall materials / materials applied in building constructions such as e.g. gypsum, plaster, stones, cement, concrete, wood, resins, wallpaper and materials applied in kits.
  • the surface of the material is cleaned to remove dirt and grease, prior to application of a paint composition according to the invention.
  • the surface may be roughened, if required, as is known to a person skilled in the art, prior to application of a paint composition according to the invention.
  • a primer might be applied to ensure better adhesion of paint to the surface.
  • Preferred glass objects include, but are not limited to, mirrors, tabletops, vases and windowpanes.
  • Preferred metal objects include, but are not limited to, appliances, barbecue grills, bicycles, fences, file cabinets, fireplace screens, hardware, light fixtures, radiators, buckets and cans.
  • Preferred plastic objects include, but are not limited to, acrylic, automotive parts, fiberglass, garbage cans, laminates, mini-blinds, outdoor furniture and shutters.
  • Preferred porcelain and ceramic objects include, but are not limited to, brick, bathtubs, flowerpots, lamp bases, servingware, sinks and tiles.
  • Preferred wooden objects include, but are not limited to, cork, finished and unfinished wooden pieces, MDF, wicker, wood composite.
  • the invention further provides the use of a paint composition comprising a pigment and a polyelectrolyte complex of a polyanion and a polycation, whereby the poly anion and the polycation are present in a relative amount of between 1:2 and 60: 1 (w/w) for painting of an object.
  • the invention further provides a painted object comprising a pigment and a polyelectrolyte complex of a polyanion and a polycation, whereby the polyanion and the polycation are present in a relative amount of between 1:2 and 60: 1 (w/w).
  • the paint composition comprising a pigment and a polyelectrolyte complex will form a film on the object that is painted.
  • a dried paint film comprising an antimicrobial agent, a pigment and a
  • polyelectrolyte complex is capable of reducing gram positive bacteria, gram negative bacteria, and viruses by greater than 3 logs within 2 hours of application.
  • the bacterial and viral reduction is measured in a test based on the JiS Z 2801 modified for paints as described herein and compared to a control paint that does not contain an antimicrobial agent such as a quaternary ammonium compound.
  • the formed precipitate is crushed by milling in the presence of Tamol (SIC), a dispersing agent from Rohm and Haas Company, and Triton, a wetting agent from Union Carbide Corporation (UCC), and in the presence or absence of chlorothalonil (CTL). Titanium oxide is added as a pigment.
  • SIC Tamol
  • SIC dispersing agent from Rohm and Haas Company
  • Triton a wetting agent from Union Carbide Corporation
  • CTL chlorothalonil
  • compositions are generated:
  • the hardness of the paint is evaluated by touching with a finger on the basis of the following criteria.
  • the acid resistance is tested by placing a 40% sulfuric acid aqueous solution (0.2 ml) as a spot on the test sheet, followed by heating to 60°C for 15 minutes, rinsing with water, and visually scoring the extent to which a mark has been produced.
  • the weatherability of the paint film is assessed visually after being exposed using standard procedures, scuh as ASTM D1006 / D1006M - 13 for conducting exterior exposure tests of paints on wood.
  • the results show that a combination of Chitosan - Calcium-lignosulfonate complex and cblorothalonil (composition A) improves the acid resistance and weatherability of the paint on the paint surface, compared to the controls.
  • compositions A-D The anti-fungal activity is determined by adding 100 spores of Stachybotrys chartarum produced using well known methods per gram of paint to compositions A-D:
  • composition A 3 wooden plywood boards (9.5cm x 9.5cm) are painted with approximately 2 gram of paint for each of the compositions.
  • the paint is allowed to dry overnight at RT.
  • the painted boards are stored at 25 °C at a humidity of at least 90%.
  • the growth on the painted boards is detected visually by eye, and the number of colonies is counted.
  • the results show that a combination of Chitosan - Calcium-lignosulfonate complex and chlorothalonil (composition A) significantly inhibits the growth of fungi on the paint surface, compared to the controls.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Plant Pathology (AREA)
  • Paints Or Removers (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

La présente invention concerne une composition de peinture comprenant un pigment et un complexe polyélectrolyte d'un polyanion et d'un polycation. L'invention concerne en outre des procédés de production de la composition de peinture, des procédés de production d'un objet peint par l'application de la composition de peinture, l'utilisation de la composition de peinture, et un objet peint comprenant un pigment et un complexe polyélectrolyte.
PCT/NL2014/050605 2013-09-04 2014-09-04 Composition de peinture comprenant un complexe polyélectrolyte WO2015034357A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP13183016 2013-09-04
EP13183016.8 2013-09-04

Publications (1)

Publication Number Publication Date
WO2015034357A1 true WO2015034357A1 (fr) 2015-03-12

Family

ID=49084906

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/NL2014/050605 WO2015034357A1 (fr) 2013-09-04 2014-09-04 Composition de peinture comprenant un complexe polyélectrolyte

Country Status (1)

Country Link
WO (1) WO2015034357A1 (fr)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017143438A1 (fr) 2016-02-23 2017-08-31 Matripharm International Inc. Composition à double vitesse de libération et à forte charge médicamenteuse
CN110093056A (zh) * 2019-05-27 2019-08-06 河北青竹画材科技有限公司 水性无甲醛绘画颜料及其制备方法
US11319673B2 (en) 2016-08-24 2022-05-03 Organoclick Ab Bio-based PEC compositions as binders for fiber based materials, textiles, woven and nonwoven materials
US11357718B2 (en) 2016-07-28 2022-06-14 eXion labs Inc. Polymer-based antimicrobial compositions and methods of use thereof
US11525211B2 (en) 2016-08-24 2022-12-13 Organoclick Ab Bio-based polyelectrolyte complex compositions comprising non-water soluble particles
US11685820B2 (en) 2016-08-24 2023-06-27 Organoclick Ab Bio-based polyelectrolyte complex compositions with increased hydrophobicity comprising fatty compounds
EP4299680A1 (fr) * 2022-06-29 2024-01-03 Saint-Gobain Weber France Composition aqueuse à réglage rapide comprenant des coacervats polyélectrolytes et des polyphénols

Citations (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3467604A (en) * 1967-07-13 1969-09-16 Amicon Corp Moisture permeable polyion complex-resinous composites
US3639263A (en) 1968-07-31 1972-02-01 Nalco Chemical Co Corrosion inhibition with a tannin, cyanohydrinated lignosulfonate, and an inorganic metal salt composition
US3923532A (en) 1974-10-21 1975-12-02 American Can Co Zinc lignosulfonate stabilizing binder solution for magnesium oxide refractory forming mixtures and method
US4006779A (en) 1975-06-30 1977-02-08 Texaco Inc. Lignosulfonates as sacrificial agents in oil recovery processes
US4017475A (en) 1975-01-20 1977-04-12 Georgia-Pacific Corporation Lignin composition and a process for its preparation
US4019995A (en) 1974-02-04 1977-04-26 Georgia-Pacific Corporation Lignosulfonate composition and process for its preparation
US4069217A (en) 1976-03-29 1978-01-17 American Can Company Solubilized lignosulfonate derivatives
US4088640A (en) 1976-06-18 1978-05-09 American Can Company Ozonated lignosulfonates
US4133385A (en) 1976-11-26 1979-01-09 Texaco Inc. Oxidized lignosulfonates as additives in oil recovery processes involving chemical recovery agents
US4181652A (en) 1976-06-18 1980-01-01 American Can Company Ozonated lignosulfonates
US4186242A (en) 1976-03-08 1980-01-29 Georgia-Pacific Corporation Preparation of a lignocellulosic composite
US4196777A (en) 1975-06-30 1980-04-08 Texaco Inc. Oxidized lignosulfonates as additives in oil recovery processes involving chemical recovery agents
US4219471A (en) 1978-02-09 1980-08-26 American Can Company Lignosulfonate derivatives
US4236579A (en) 1978-05-30 1980-12-02 Texaco Inc. Modified lignosulfonates as additives in oil recovery processes involving chemical recovery agents
US4249606A (en) 1979-11-05 1981-02-10 Texaco Inc. Lignosulfonates carboxylated with carbon dioxide as additives in oil recovery processes involving chemical recovery agents
US4250088A (en) 1979-08-20 1981-02-10 American Can Company Demethylated lignin and process
US4267886A (en) 1978-04-27 1981-05-19 Texaco Inc. Lignosulfonates carboxylated with chloroacetic acid as additives in oil recovery processes involving chemical recovery agents
US4269270A (en) 1978-04-28 1981-05-26 Texaco Inc. Sulfomethylated lignosulfonates as additives in oil recovery processes involving chemical recovery agents
US4293342A (en) 1978-02-09 1981-10-06 American Can Company Lignosulfonate derivatives
US4336189A (en) 1979-05-28 1982-06-22 Oy Tampella Ab Process for recovering lignosulfonates from spent sulfite liquor
US4344487A (en) 1976-11-26 1982-08-17 Texaco Inc. Modified lignosulfonates as additives in oil recovery processes involving chemical recovery agents
US4594168A (en) 1980-02-27 1986-06-10 L'avebene Derivatives of lignosulfonic acid
US4666522A (en) 1985-02-13 1987-05-19 Reed Lignin Inc. Stable lignosulfonate emulsion
US4786438A (en) 1983-03-08 1988-11-22 Georgia-Pacific Corporation Lignosulfonate/urea binder for particulate composites
US5032164A (en) 1990-05-25 1991-07-16 Daishowa Chemicals, Inc. Modified lignosulfonate conditioning agent for urea particles
US5075402A (en) 1989-03-27 1991-12-24 Ligno Tech. U.S.A. Non-toxic, stable lignosulfonate-urea-formaldehyde composition and method of preparation thereof
US5286412A (en) 1991-10-16 1994-02-15 Georgia-Pacific Corporation Modified lignosulfonate dispersant for gypsum
US5401718A (en) 1992-11-24 1995-03-28 Patel; Bharat B. Tin/cerium compounds for lignosulfonate processing
US5446133A (en) 1990-09-06 1995-08-29 Lignotech Usa, Inc. Nitric acid oxidized lignosulfonates
US5578598A (en) * 1990-11-29 1996-11-26 Iatron Laboratories, Inc. Polyelectrolyte complex antibacterial agent in antibacterial material
US5981433A (en) 1995-06-29 1999-11-09 Rhone-Poulenc Chimier Lignosulfonate/ethoxylated poly(1-phenylethyl)phenol dispersing agents and agrochemicals comprised thereof
US6030738A (en) * 1997-07-31 2000-02-29 Clariant Gmbh Use of inter-polyelectrolyte complexes as charge control agents
US6420602B1 (en) 1999-02-03 2002-07-16 Ucb, S.A. Method for the production of tetramethylthiuram disulfide
US7238645B1 (en) 2000-09-18 2007-07-03 Syngenta Crop Protection, Inc. Pesticide formulations containing phosphate ester surfactant and alkoxylated lignosulfonate
EP1834994A1 (fr) * 2006-03-15 2007-09-19 Clariant International Ltd. Pigments encapsules en polyelectrolytes
US20070243237A1 (en) * 2006-04-14 2007-10-18 Mazen Khaled Antimicrobial thin film coating and method of forming the same
US20070259016A1 (en) * 2006-05-05 2007-11-08 Hodge Robert L Method of treating crops with submicron chlorothalonil
US7727966B2 (en) 2004-10-28 2010-06-01 Dsm Ip Assets B.V. Stable needle-shaped crystals of natamycin
DE102010001891A1 (de) * 2010-02-12 2011-08-18 Leibniz-Institut für Polymerforschung Dresden e.V., 01069 Dispergiermittel zur Stabilisierung von Dispersionen

Patent Citations (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3467604A (en) * 1967-07-13 1969-09-16 Amicon Corp Moisture permeable polyion complex-resinous composites
US3639263A (en) 1968-07-31 1972-02-01 Nalco Chemical Co Corrosion inhibition with a tannin, cyanohydrinated lignosulfonate, and an inorganic metal salt composition
US4019995A (en) 1974-02-04 1977-04-26 Georgia-Pacific Corporation Lignosulfonate composition and process for its preparation
US3923532A (en) 1974-10-21 1975-12-02 American Can Co Zinc lignosulfonate stabilizing binder solution for magnesium oxide refractory forming mixtures and method
US4017475A (en) 1975-01-20 1977-04-12 Georgia-Pacific Corporation Lignin composition and a process for its preparation
US4006779A (en) 1975-06-30 1977-02-08 Texaco Inc. Lignosulfonates as sacrificial agents in oil recovery processes
US4196777A (en) 1975-06-30 1980-04-08 Texaco Inc. Oxidized lignosulfonates as additives in oil recovery processes involving chemical recovery agents
US4186242A (en) 1976-03-08 1980-01-29 Georgia-Pacific Corporation Preparation of a lignocellulosic composite
US4069217A (en) 1976-03-29 1978-01-17 American Can Company Solubilized lignosulfonate derivatives
US4181652A (en) 1976-06-18 1980-01-01 American Can Company Ozonated lignosulfonates
US4088640A (en) 1976-06-18 1978-05-09 American Can Company Ozonated lignosulfonates
US4133385A (en) 1976-11-26 1979-01-09 Texaco Inc. Oxidized lignosulfonates as additives in oil recovery processes involving chemical recovery agents
US4344487A (en) 1976-11-26 1982-08-17 Texaco Inc. Modified lignosulfonates as additives in oil recovery processes involving chemical recovery agents
US4293342A (en) 1978-02-09 1981-10-06 American Can Company Lignosulfonate derivatives
US4219471A (en) 1978-02-09 1980-08-26 American Can Company Lignosulfonate derivatives
US4267886A (en) 1978-04-27 1981-05-19 Texaco Inc. Lignosulfonates carboxylated with chloroacetic acid as additives in oil recovery processes involving chemical recovery agents
US4269270A (en) 1978-04-28 1981-05-26 Texaco Inc. Sulfomethylated lignosulfonates as additives in oil recovery processes involving chemical recovery agents
US4236579A (en) 1978-05-30 1980-12-02 Texaco Inc. Modified lignosulfonates as additives in oil recovery processes involving chemical recovery agents
US4336189A (en) 1979-05-28 1982-06-22 Oy Tampella Ab Process for recovering lignosulfonates from spent sulfite liquor
US4250088A (en) 1979-08-20 1981-02-10 American Can Company Demethylated lignin and process
US4249606A (en) 1979-11-05 1981-02-10 Texaco Inc. Lignosulfonates carboxylated with carbon dioxide as additives in oil recovery processes involving chemical recovery agents
US4594168A (en) 1980-02-27 1986-06-10 L'avebene Derivatives of lignosulfonic acid
US4786438A (en) 1983-03-08 1988-11-22 Georgia-Pacific Corporation Lignosulfonate/urea binder for particulate composites
US4666522A (en) 1985-02-13 1987-05-19 Reed Lignin Inc. Stable lignosulfonate emulsion
US5075402A (en) 1989-03-27 1991-12-24 Ligno Tech. U.S.A. Non-toxic, stable lignosulfonate-urea-formaldehyde composition and method of preparation thereof
US5032164A (en) 1990-05-25 1991-07-16 Daishowa Chemicals, Inc. Modified lignosulfonate conditioning agent for urea particles
US5446133A (en) 1990-09-06 1995-08-29 Lignotech Usa, Inc. Nitric acid oxidized lignosulfonates
US5578598A (en) * 1990-11-29 1996-11-26 Iatron Laboratories, Inc. Polyelectrolyte complex antibacterial agent in antibacterial material
US5286412A (en) 1991-10-16 1994-02-15 Georgia-Pacific Corporation Modified lignosulfonate dispersant for gypsum
US5401718A (en) 1992-11-24 1995-03-28 Patel; Bharat B. Tin/cerium compounds for lignosulfonate processing
US5981433A (en) 1995-06-29 1999-11-09 Rhone-Poulenc Chimier Lignosulfonate/ethoxylated poly(1-phenylethyl)phenol dispersing agents and agrochemicals comprised thereof
US6030738A (en) * 1997-07-31 2000-02-29 Clariant Gmbh Use of inter-polyelectrolyte complexes as charge control agents
US6420602B1 (en) 1999-02-03 2002-07-16 Ucb, S.A. Method for the production of tetramethylthiuram disulfide
US7238645B1 (en) 2000-09-18 2007-07-03 Syngenta Crop Protection, Inc. Pesticide formulations containing phosphate ester surfactant and alkoxylated lignosulfonate
US7727966B2 (en) 2004-10-28 2010-06-01 Dsm Ip Assets B.V. Stable needle-shaped crystals of natamycin
EP1834994A1 (fr) * 2006-03-15 2007-09-19 Clariant International Ltd. Pigments encapsules en polyelectrolytes
US20070243237A1 (en) * 2006-04-14 2007-10-18 Mazen Khaled Antimicrobial thin film coating and method of forming the same
US20070259016A1 (en) * 2006-05-05 2007-11-08 Hodge Robert L Method of treating crops with submicron chlorothalonil
DE102010001891A1 (de) * 2010-02-12 2011-08-18 Leibniz-Institut für Polymerforschung Dresden e.V., 01069 Dispergiermittel zur Stabilisierung von Dispersionen

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
ALEXANDRE DROGOZ ET AL: "Polyelectrolyte Complexes from Polysaccharides: Formation and Stoichiometry Monitoring", LANGMUIR, AMERICAN CHEMICAL SOCIETY, NEW YORK, NY; US, vol. 23, no. 22, 23 October 2007 (2007-10-23), pages 10950 - 10958, XP002657434, ISSN: 0743-7463, [retrieved on 20070920], DOI: 10.1021/LA7008545 *
DAUTZENBERG H ET AL: "Stoichiometry and structure of polyelectrolyte complex particles in diluted solutions", BERICHTE DER BUNSEN-GESELLSCHAFT FUR PHYSIKALISCHE CHEMIE, VERLAG CHEMIE. WEINHEIM, DE, vol. 100, no. 6, 1 June 1996 (1996-06-01), pages 1024 - 1032, XP002967282, ISSN: 0005-9021 *
GURO E. FREDHEIM ET AL: "Polyelectrolyte Complexes: Interactions between Lignosulfonate and Chitosan", BIOMACROMOLECULES, vol. 4, no. 2, 31 January 2003 (2003-01-31), pages 232 - 239, XP055026736, ISSN: 1525-7797, DOI: 10.1021/bm020091n *

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017143438A1 (fr) 2016-02-23 2017-08-31 Matripharm International Inc. Composition à double vitesse de libération et à forte charge médicamenteuse
EP3419669A4 (fr) * 2016-02-23 2019-10-30 Matripharm International Inc. Composition à double vitesse de libération et à forte charge médicamenteuse
US11357718B2 (en) 2016-07-28 2022-06-14 eXion labs Inc. Polymer-based antimicrobial compositions and methods of use thereof
US11426343B2 (en) 2016-07-28 2022-08-30 eXion labs Inc. Polymer-based antimicrobial compositions and methods of use thereof
US11319673B2 (en) 2016-08-24 2022-05-03 Organoclick Ab Bio-based PEC compositions as binders for fiber based materials, textiles, woven and nonwoven materials
US11525211B2 (en) 2016-08-24 2022-12-13 Organoclick Ab Bio-based polyelectrolyte complex compositions comprising non-water soluble particles
US11685820B2 (en) 2016-08-24 2023-06-27 Organoclick Ab Bio-based polyelectrolyte complex compositions with increased hydrophobicity comprising fatty compounds
CN110093056A (zh) * 2019-05-27 2019-08-06 河北青竹画材科技有限公司 水性无甲醛绘画颜料及其制备方法
CN110093056B (zh) * 2019-05-27 2021-06-08 河北青竹画材科技有限公司 水性无甲醛绘画颜料及其制备方法
EP4299680A1 (fr) * 2022-06-29 2024-01-03 Saint-Gobain Weber France Composition aqueuse à réglage rapide comprenant des coacervats polyélectrolytes et des polyphénols
WO2024003041A1 (fr) * 2022-06-29 2024-01-04 Saint-Gobain Weber France Composition aqueuse à prise rapide comprenant des coacervats de polyélectrolyte et des polyphénols

Similar Documents

Publication Publication Date Title
WO2015034357A1 (fr) Composition de peinture comprenant un complexe polyélectrolyte
CA2282462C (fr) Prevention de la decoloration dans des compositions de revetement contenant de la pyrithione
WO2014209222A1 (fr) Composition de revêtement antimicrobien
JP5529834B2 (ja) グリホサート化合物とzptとの相乗的組み合わせ
CN107936663A (zh) 掺有一种或更多种抗菌生物表面活性剂的水性涂料和油漆、及其使用方法
CN103897538B (zh) 一种保护型水性抗菌防霉涂料及其制备方法
CN109476932B (zh) 抗微生物涂料组合物及相关方法
JP2007084823A (ja) アルカリ性コーティング組成物の殺カビ性および殺藻性仕上げのための組成物
JP5529831B2 (ja) グリホサート化合物とipbcとの相乗的組み合わせ
US11566140B2 (en) Exterior coating composition
RU2329286C1 (ru) Способ пролонгированной дезинфекции помещений, оборудования, консервации и обеззараживания воды
KR20080077682A (ko) 신규한 물질 및 이의 제조방법
EP0979033A1 (fr) Conservateur algicide et fongicide a activite anti-alternaria
PL160910B1 (pl) Srodek do zwalczania drobnoustrojów PL PL PL PL
KR101362849B1 (ko) 글리포세이트 화합물과 tbz의 상승적 배합물
JP5529832B2 (ja) Dcoitまたはoitまたはbbitの1種と、グリホサート化合物との相乗的組み合わせ
JP5529833B2 (ja) グリホサート化合物とdmitsとの相乗的組み合わせ
KR20210074305A (ko) 규회석을 포함하는 항균 조성물
JP2019528266A (ja) レナシルおよび1,2−ベンズイソチアゾール−3(2h)−オンの相乗的組み合わせ
RU2491244C1 (ru) Шпатлевочная масса
JP4338461B2 (ja) 工業用抗菌組成物
WO2024006517A1 (fr) Composés contenant du cuivre et compositions pour peinture et revêtement antimicrobiens
EP4217432A1 (fr) Compositions de revêtement contenant du chitosane
JPH0242004A (ja) 塗料用防カビおよび防藻組成物
HU203572B (en) Dispersive distemper of retard bactericide fungicide activity

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 14777193

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 14777193

Country of ref document: EP

Kind code of ref document: A1