WO2012167786A1 - Base huileuse pour peintures à l'huile - Google Patents

Base huileuse pour peintures à l'huile Download PDF

Info

Publication number
WO2012167786A1
WO2012167786A1 PCT/DK2011/000058 DK2011000058W WO2012167786A1 WO 2012167786 A1 WO2012167786 A1 WO 2012167786A1 DK 2011000058 W DK2011000058 W DK 2011000058W WO 2012167786 A1 WO2012167786 A1 WO 2012167786A1
Authority
WO
WIPO (PCT)
Prior art keywords
oil
naturally occurring
amount
green
yellow
Prior art date
Application number
PCT/DK2011/000058
Other languages
English (en)
Inventor
Christina Haack CHRISTENSEN
Original Assignee
CHRISTINA COLOR DENMARK ApS
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 CHRISTINA COLOR DENMARK ApS filed Critical CHRISTINA COLOR DENMARK ApS
Priority to PCT/DK2011/000058 priority Critical patent/WO2012167786A1/fr
Publication of WO2012167786A1 publication Critical patent/WO2012167786A1/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
    • C09D5/06Artists' paints
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00Compositions of oils, fats or waxes; Compositions of derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00Compositions of oils, fats or waxes; Compositions of derivatives thereof
    • C08L91/06Waxes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L93/00Compositions of natural resins; Compositions of derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L93/00Compositions of natural resins; Compositions of derivatives thereof
    • C08L93/02Shellac
    • 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
    • C09D191/00Coating compositions based on oils, fats or waxes; Coating compositions based on 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
    • C09D191/00Coating compositions based on oils, fats or waxes; Coating compositions based on derivatives thereof
    • C09D191/06Waxes
    • 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
    • C09D193/00Coating compositions based on natural resins; Coating compositions based on 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
    • C09D193/00Coating compositions based on natural resins; Coating compositions based on derivatives thereof
    • C09D193/02Shellac
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J191/00Adhesives based on oils, fats or waxes; Adhesives based on derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J191/00Adhesives based on oils, fats or waxes; Adhesives based on derivatives thereof
    • C09J191/06Waxes
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J193/00Adhesives based on natural resins; Adhesives based on derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J193/00Adhesives based on natural resins; Adhesives based on derivatives thereof
    • C09J193/02Shellac
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/08Metals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/02Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group

Definitions

  • the present invention relates to the field of artistic oil paints and oil bases for artistic oil paints. More specifically, the present invention relates to a method for the manufacture of an oil base for artistic oil paints, such an oil base per se as well as uses thereof.
  • oils used for the paint must have sufficient amount of triglycerides having a sufficient number of double bonds.
  • the drying of an oil paint involves formation of cross linking of the carbon chains of the triglycerides of the oil used by oxidation of the double bonds of the oil's fatty acids. For this reason, in order to ensure that the oil paint is capable of drying and capable of drying within a not too long period of time, the carbon chains of the triglycerides of the oil used must comprise a sufficient number of double bonds enabling such cross linking.
  • the drying process involving the cross linking is effected by oxidation of the double bonds by the air's oxygen.
  • the oil used for oil paints is linseed oil which has been heated to about 300 °C for a few days in the complete absence of air.
  • the resulting oil is called stand oil.
  • the stand oil has a sufficient amount of double bonds in the carbon chains of its fatty acid esters that allows the oil and hence also the corresponding paint made therewith to dry and harden upon exposure to air
  • oil paints have a propensity to blend into surrounding paint allowing very subtle blending of colours and thereby producing vivid colours with a natural sheen and distinct contrast makes oil paint based on stand oil the preferred technique to use by many artists.
  • oil paints indeed is capable of drying by exposure to air, the drying process is rather slow and when the drying is effected solely by exposure of the paint to the air's oxygen, the paint may take weeks to dry. For this reason, artists using oil paints based on stand oil usually add one or more drying agents to the paints when mixing the colours on the palette. The drying agent(s) added will considerably speed up the drying process.
  • drying agents traditionally added to the paints prior to application to the canvas are derived from cobalt, manganese, lead, zirconium, zinc, calcium and iron in the form of coordination complexes. These complexes are typically suspended in a volatile organic medium, such as turpentine or xylol.
  • drying agents examples include siccative and liquin. It is clear that the necessity of adding volatile organic solvents to the drying agents poses a health risk for the painting artist. This heath risk is related to the exposure of vapours of the organic solvents which may very well enter the human respiratory system and hence damage the human body.
  • Acrylic paints are based on coloured pigments or dyes suspended in an acrylic polymer suspension, optionally also comprising water. Unlike oil paints, acrylic paints are fast drying and does not necessitate the use of drying agents comprising organic solvents.
  • an oil base which according to a first aspect of the present invention is manufactured by a process comprising the steps: i) providing an amount of stand oil; ii) providing an amount of naturally occurring resins, said resins comprise at least 10 wt% of sandarac resin, mastic resin or a mixture thereof, based on the total amount of naturally occurring resins; iii) providing an amount of naturally occurring waxes, said naturally occurring waxes comprise at least 10 wt% of beeswax based on the total amount of naturally occurring waxes; iv) mixing said amount of stand oil provided in step i) with said amount of naturally occurring resins provided in step ii) and said amount of naturally occurring waxes provided in step iii); v) carefully stirring the mixture obtained in step iv) at a temperature which enables obtaining a homogeneous mixture; vi) optionally cooling the homogeneous mixture obtained in the previous step to
  • the present invention relates to the use of an oil base according to the second aspect of the present invention for artistic oil painting.
  • the present invention relates to a canvas for artistic oil painting wherein said canvas comprises an application of the oil base according to the second aspect of the present invention.
  • the present invention relates to a paint for artistic oil painting comprising an oil base according the second aspect of the present invention and one or more colouring agents.
  • the oil base of the second aspect of the present invention is in itself a whitish, partly transparent cream-like composition.
  • the oil base of the second aspect of the present invention is 100% non-toxic and its production and uses is environmentally friendly and can be used with any given additive such as a colouring agent as disclosed in a later paragraph.
  • the oil base of the second aspect of the present invention has great advantages in uses in artistic oil painting because the health risks traditionally associated with the necessary use of drying agents can be completely eliminated as disclosed in later paragraphs.
  • the oil base itself according to the second aspect of the present invention is environmentally friendly and comprises no poisonous ingredients.
  • the oil base virtually has no smell and it is completely miscible with additives traditionally and/or conventionally used in artistic painting, such as matting or glossing additives or the like.
  • the oil base of the second aspect of the present invention is a partly transparent paste-like cream.
  • the oil base can be manufactured in a way that makes it very viscous and dense. This has the advantage that in case the oil base is used for an oil paint, an artist upon use of the oil paint for an artistic painting can use that oil paint as is and smear it onto the canvas if he wished thick layers of paint. Alternatively, he can choose to blend in an amount of oil, such as bleached linseed oil, or even water in case the artist wishes to perform thin silk-like layers onto the canvas.
  • the oil base and the oil paints manufactured thereof additionally accordingly exhibits a modelling effect that allows an artist to shape the oil base or the paint applied to the canvas in a desired shape and the oil base or the oil paint will retain its shape and dry while maintaining the shape. These properties are highly desirable because if gives the artist great flexibility in adjusting the visual depth of each stroke performed with the brush. The drying itself will occur without any running of the oil base or paint and without any oozing of oily constituents from the oil base or from the paint.
  • oil base and the oil paints made therefrom do not make colours flow or drip when blending with similar paints of different colours.
  • All in all the oil base according to the second aspect of the present invention and the oil paints made therefrom according to a fifth aspect represents a high degree of flexibility for an artist making an oil painting without the known hazards relating to volatile organic solvents involved in traditional and conventional oil painting. Detailed description of the invention
  • the present invention relates to a method for the manufacture of an oil base for use in artistic oil painting, said method comprising the steps: i) providing an amount of stand oil; ii) providing an amount of naturally occurring resins, said resins comprise at least 10 wt% of sandarac resin, mastic resin or a mixture thereof, based on the total amount of naturally occurring resins; iii) providing an amount of naturally occurring waxes, said naturally occurring waxes comprise at least 10 wt% of beeswax based on the total amount of naturally occurring waxes; iv) mixing said amount of stand oil provided in step i) with said amount of naturally occurring resins provided in step ii) and said amount of naturally occurring waxes provided in step iii); v) carefully stirring the mixture obtained in step iv) at a temperature which enables obtaining a homogeneous mixture; vi) optionally cooling the homogeneous mixture obtained in the previous step to room temperature; vii) subject
  • the oil base so obtained is beneficial in its various uses in art painting because the desired visual effects of traditional oil painting paints can be attained with the oil base obtained according to the first aspect of the present invention without the detrimental effect of the necessity of using volatile organic drying agents and/or turpentine in order to speed up the drying process of the oil paint.
  • step i), ii) and iii) of the method of the first aspect of the present invention the starting constituents are provided.
  • the amount of stand oil is 9 - 99 wt% based on the combined amount of said stand oil, said naturally occurring resins, and said naturally occurring waxes mixed in step iv) of said method.
  • said amount of stand oil is 10 - 95 wt%, such as 15 - 90 wt%, e.g. 20 - 85 wt%, such as 25 - 80 wt%, for example 30 - 75 wt%, such as 35 - 70 wt%, e.g. 40 - 65 wt%, such as 45 - 60 wt% or 50 - 55 wt% based on the combined amount of said stand oil, said naturally occurring resins, and said naturally occurring waxes mixed in step iv) of said method.
  • Stand oil originates from linseed oil and is generated by heating linseed oil near 300°C for a few days in the complete absence of air. Under these conditions, a crosslinking of the polyunsaturated fatty ester residues takes place. Stand oil is readily commercially available.
  • the amount of the naturally occurring resins is 0.02 - 85 wt% based on the combined amount of said stand oil, said naturally occurring resins, and said naturally occurring waxes mixed in step iv) of said method.
  • said amount of the naturally occurring resins is 0.5 - 80 wt%, such as 1 - 75, for example 5 - 70 wt%, such as 10 - 65 wt%, such as 15 - 60 wt%, for example 20 - 55 wt%, e.g. 25 - 50 wt%, such as 30 - 45 wt% or 35 - 40 wt%, based on the combined amount of said stand oil, said naturally occurring resins, and said naturally occurring waxes mixed in step iv) of said method.
  • the amount of the naturally occurring waxes is 0.3 - 78 wt% based on the combined amount of said stand oil, said naturally occurring resins, and said naturally occurring waxes mixed in step iv) of said method.
  • said amount of the naturally occurring waxes is 0.5 - 75 wt%, such as 0.7 - 70, such as 1 - 65, for example 5 - 60, such as 10 - 55, for example 15 - 50, such as 20 - 45, such as 25 - 40 or 30 - 35, based on the combined amount of said stand oil, said naturally occurring resins, and said naturally occurring waxes mixed in step iv) of said method.
  • said naturally occurring resins provided in step ii) are selected from the group comprising: sandarac, mastic, dammar, shellac, colophonium, xanthorrhoea resins.
  • the naturally occurring waxes provided in step iii) are selected from the group comprising: beeswax, canauba wax, candelilla wax.
  • step iv) and v) of the method according to the first aspect of the present invention the constituents provided in step i), ii) and ii) are mixed and stirred.
  • the temperature of the mixture in step v) is 25 - 90 °C, such as 30 - 85 °C, e.g. 35 - 80 °C, such as 40 - 75 °C, for example 45 - 70 °C, e.g. 50 - 65 °C, such as 55 - 60 °C.
  • step v) of the method of the first aspect according to the present invention is performed essentially without aerating said mixture.
  • step v) is performed for a period of time of 5 sec. to 190 sec, such as 10 - 180 sec, for example 20 - 170 se , such as 30 - 160 sec, e.g. 40 - 150 sec, such as 50 - 140 sec, for example 60 - 130 sec, e.g. 70 - 120 sec, such as 80 - 1 10 sec. or 90 - 100 sec.
  • the naturally occurring resin(s) prior to blending with the stand oil and the naturally occurring wax(es) is/are dissolved or suspended in an amount of linseed oil varnish.
  • the amount of linseed oil varnish dissolving or suspending the naturally occurring resin(s) is 0.1 - 10 wt% of the amount of the naturally occurring resin(s), such as 0.2 - 8 wt%, e.g. 0.5 - 7 wt%, such as 1 - 6 wt%, e.g. 2 - 5 wt%, such as 3 - 4 wt% of the amount of the naturally occurring resin(s).
  • the natural occurring resins are first mixed with stand oil comprising an amount of linseed oil varnish, optionally by heating, for facilitating dissolution or suspension thereof.
  • the process prior to step vi) comprises the step of heating the mixture to a temperature of 60 - 90 °C, whereafter one or more metals are added and subsequently stirred in carefully, said metal preferably being a metal selected from the group comprising: copper, aluminium, magnesium, silver, gold, optionally in the form of an alloy, such as bronze. It has been found that adding one or metals at this stage will enhance the drying properties of the resulting oil base.
  • said metal is present in an amount of 0.5 - 7 wt%, such as 1 - 6 wt%, such as 2 - 5 wt%, e.g. 3 - 4 wt% based on the combined amount of stand oil, naturally occurring resins, and naturally occurring waxes mixed in step iv) of said process.
  • said metal or alloy is a pulverised metal or alloy.
  • a preservative is added to the mixture, preferably subsequent to step vi).
  • the preservative is selected from the group comprising: sodium benzoate.
  • Sodium benzoate has been found to be an extremely effective and inexpensive preservative to be used with the oil base obtained in the method of the first aspect of the present invention.
  • any other kind of suitable preservative may be added. The preservative ensures that the oil base can be shelved for years without any changes caused by microorganisms taking place.
  • the mixture obtained in step vi) is allowed to rest and solidify.
  • the manufacturing process is paused for a period of time after step vi) of said method.
  • the mixture is allowed to rest and solidify for a period of time of 1 hour to 2 months or more.
  • a resting time of 2 hours - 50 days such as 4 hours to 30 days, such as 8 hours to 25 days, such as 12 hours to 20 days, for example 18 hours to 15 days, such as 1 days to 10 days, such as 2 days to 8 days, such as 4 days to 6 days may be possible.
  • additional oil such as stand oil immediately prior to the application of the oil base.
  • the mixing in of additional stand oil prior to use of the final oil base allows to adjust the plasticity or the viscosity of the oil base. The better the ability to take up additional oil prior to application of the oil base, the greater span of plasticity of the oil base can be obtained.
  • step vi) it is important to note that it is paramount that the final oil base after application thereof does not ooze out any oil or other constituent.
  • the mixture obtained in step vi) is allowed to rest and solidify for a specific period of time it may be appropriate - before resuming the rest of the method, i.e. at least step vii) - to melt the solidified mixture.
  • metal is added prior to step vi) and furthermore, the mixture obtained in step vi) is allowed to rest and solidify for a specific period of time.
  • This embodiment of the method according to the present invention will ensure a faster and more homogeneous drying of the oil base.
  • an additional oil is added to the mixture of the stand oil, the resin(s) and the wax(es) prior to step vii).
  • said additional oil is selected from the group comprising sunflower oil, paraffin oil and castor oil and mixtures thereof.
  • Step vi) of the method according to the first aspect of the present invention is optional and involves cooling the mixture obtained to room temperature.
  • This step is preferably performed in a case where the mixture is allowed to rest and solidify before performing step vii) of the method according to the first aspect of the present invention.
  • Step vii) of the method according to the first aspect of the present invention involves subjecting the mixture obtained to a steam blowing process.
  • the steam blowing process simply may be performed by boiling an amount of water and leading the obtained water steam into the mixture obtained in step v) or vi).
  • the steam blowing results in a waxy material of water and the constituents provided in step i), ii) and iii) and any other constituents added during the steps of the method.
  • This material may be describes as a matrix of water and said constituents, where the constituents may together have undergone further physical and chemical changes, intermolecular as well as intramolecular.
  • liquid water is added in step vii) of said method, preferably demineralised liquid water.
  • the amount of liquid water added may be 1 - 10 wt%, such as 2 - 9 wt%, for example 3 - 8 wt%, such as 4 - 7 wt%, such as 5 - 6 wt% based on the combined amount of said stand oil, said naturally occurring resins, and said naturally occurring waxes mixed in step iv).
  • additional stand oil is added in step vii) of said method.
  • the amount of additional stand oil is 0.01 - 10 wt%, such as 0.5 - 9 wt%, e.g. 1 - 8 wt%, such as 2 - 7 wt%, for example 3 - 6 wt%, such as 4 - 5 wt% based on the combined amount of said stand oil, said naturally occurring resins, and said naturally occurring waxes mixed in step iv).
  • the steam blowing steps is performed for a period of time of 5 sec. to 190 sec, such as 10 - 180 sec, for example 20 - 170 sec, such as 30 - 160 sec, e.g. 40 - 150 sec, such as 50 - 140 sec, for example 60 - 130 sec, e.g. 70 - 120 sec, such as 80 - 110 sec. or 90 - 100 sec.
  • the second aspect of the present invention relates to an oil base obtainable by the method according to the first aspect.
  • the steam blowing step will make the mixture hazy and waxy and it is believed that this process step is responsible for initiating further physical and chemical changes within and/or among the constituents making up the mixture to be subjected to steam blowing. For this reason, it is not possible to define the product of the second aspect of the present invention, i.e. the oil base in purely structural terms.
  • the oil base according to the second aspect of the present invention may be defined as a product comprising a steam blown mixture, said mixture originating from a homogeneous mixture of an amount of stand oil, an amount of naturally occurring resins, said resins comprise at least 10 wt% of sandarac resin, mastic resin or a mixture thereof, based on the total amount of naturally occurring resins; and an amount of naturally occurring waxes, said naturally occurring waxes comprise at least 10 wt% of beeswax based on the total amount of naturally occurring waxes.
  • the third aspect of the present invention relates to the use of an oil base as defined in the second aspect of the present invention for artistic oil painting.
  • the use relates to the preparation of a canvas for artistic oil painting.
  • the use relates to the preparation of an artistic oil painting paint.
  • the fourth aspect of the present invention relates to a canvas for artistic oil painting.
  • the canvas according to the fourth aspect of the present invention comprises a conventionally or traditionally canvas and an application of the oil base according to the second aspect of the present invention.
  • the term “canvas” shall be understood to mean any suitable material traditionally and/or conventionally used as support for oil paints in a painting.
  • the term “canvas” may mean a cloth, such as cotton or flax, such as Belgian linen; or a hard material, such as wood, a board of natural and/or synthetic fibres or any other suitable material.
  • a cloth canvas is simply obtained by suspending a traditional and/or conventional cloth on a frame, such as a wooden frame and applying a suitable amount of the oil base according to the second aspect of the present invention onto said cloth.
  • the amount of oil base applied to the canvas will suitably follow the intended thickness of oil paint to be applied to the canvas; if a relatively thick layer of oil paints is intended, a relatively thick layer of oil base is applied to the canvas and vice versa.
  • said canvas comprises an application of gesso beneath said application of said oil base.
  • said gesso is a traditional gesso or an acrylic gesso.
  • said gesso is selected from the group comprising: PVA (polyvinyl acetate), bone glue, egg tempera and a fixative.
  • PVA polyvinyl acetate
  • the canvas according to the fourth aspect of the present invention allows for painting with traditionally oil paints without the necessity of using drying agents and/or turpentine containing hazardous volatile organic solvents and with the possibility of being able to apply new layers of traditionally oil paints within as little as six hours.
  • the oil base applied to the canvas is an oil base obtained by a method according to the first aspect and in which a metal has been added prior to step vi).
  • a paint according to a fifth aspect of the present invention relates to a paint for artistic oil painting.
  • the paint according to the fifth aspect comprises an oil base according to the second aspect of the present invention and one or more colouring agents.
  • the oil painting paints are obtained by gradually blending and mixing in an amount of a specific colouring agent in a predetermined amount of oil base
  • said colouring agents are selected from the group comprising: dyes and pigments.
  • said paint additionally comprises an amount of aluminium tartrate.
  • aluminium tartrate will provide a "shadowing effect" to the oil paint as it is well known in the art of oil paints for artistic use and also tend to improve the drying ability of the oil paint.
  • the colouring agent is a white pigment.
  • Suitable white pigments may be selected from the group comprising: titanium white, titanium and zinc white, flake white hue, iridescent white, titanium white, pigment white 6, zinc white, lead white, lead carbonate.
  • the colouring agent is a blue pigment.
  • Suitable blue pigments may be selected from the group comprising: ultramarin deep, ultramarin light, ultramarine blue (green shade), Lefranc blue, cobalt blue, cobalt blue hue, royal blue, space blue, ocean blue, cerulean blue, cerulean blue heu, cobalt silicate blue, cobalt kings blue.
  • the colouring agent is a red pigment.
  • Suitable red pigments may be selected from the group comprising: Breughel red, French red vermillion hue, Red vermillion hue, Cadmium red light, Cadmium red medium, Japanese red deep, Chinese red vermillion hue, Bright red, Cadmium red deep, Lefranc red, Rose madder hue, Ruby red, Lefranc pink, Lefranc crimson, Lefranc garnet red, Alzarin carmine, Carmin lake hue, Permanent red deep, Scarlet, Carmin, Cinnober red, Perylen red Pigment, Alizarin, Crimson red, Kraplak.
  • the colouring agent is a green pigment.
  • Suitable green pigments may be selected from the group comprising: Green umbra, Terre Verte, lemon green light, cadmium green (yellowish), cadmium green, cadmium green, permanent green light. Phthlo green, Phthlo Amor green, Japanese green deep,Chrome green deep, Zink green dark, Chromgreen yellowish, Chrome Green dark / light, Chrome oxide green, Chrome oxide green, Olive green, Permanent sap green, Veronese green hue, Terre Verte, Chrome oxide
  • the colouring agent is a yellow pigment.
  • Suitable yellow pigments may be selected from the group comprising: Cadmium yellow, Nickelazo yellow, Sulphur yellow, Japanese yellow lemon, Lefranc yellow, Cadmium yellow lemon, Japanese yellow light, Cadmium yellow light, Senegal Yellow, Cadmium yellow medium, Japanese yellow deep, Chrome yellow medium hue, Indian yellow hue, Chrome Yellow deep hue, Sahara yellow, Cadmium yellow deep, Yellow ochre light, Yellow ochre, Transparent Yellow ochre, Mars Yellow, Golden ochre, Raw Sienna, Yellow ochre, Ochre hue.
  • the colouring agent is orange pigment.
  • Suitable orange pigments may be selected from the group comprising: Japanese yellow orange, Cadmium yellow orange, Bright orange, Transparent Indian orange, Coral, Mars orange, Benzidazolon orange, Quanicrondon orange, Benzimidazolon orange, Perinon orange, Isoindolinon, Chrome orange.
  • the colouring agent is a violet pigment.
  • Suitable purple pigments may be selected from the group comprising: Permanent violet, Red violet light, Cobolt violet red, Lefranc Crimson, Garnet red, Alizarin Carmine, Lefranc pink, Red violet light,Permanent rose, Red violet deep, Madder lake deep, Coboltviolet, Bluish grey Rembrandt, Cobolt violet light, Violet lacquer blue, Mineral violet light, Strong violet, Violet (blue shade), Ultramarin deep violet, Ultramarin blue 907, Ultramarin violet, Cobolt blue hue, Mauve Violet, manganese violet, Egyptian Violet hue, Dioxazin violet, Indanthron blue.
  • the colouring agent is a brown pigment.
  • Suitable brown pigments may selected from the group comprising: Permanent Vandyke brown, Transparent brown, Burnt umber, assler brown.
  • the colouring agent is a black pigment.
  • Suitable black pigments may be selected from the group comprising: Ivory Black, Carbon black, Bitumen, Asphalt Bitumen / Graphite, Mangan Black, Iron oxide black, Graphite, Peach Stone Black, Grape stone black, Cherry Stone black,
  • the colouring agent comprises graphite, said graphite preferably being present in a pulverized state and/or in an amount of 10 - 60 wt% of said oil base.
  • the colouring agent comprises bitumen, said bitumen preferably being present in an amount of 10 - 60 wt% of said oil base.
  • the colouring agent is a colouring agent providing a metallic colour, such as a golden colour, a silver colour, a bronze-like colour or a copper-like colour, said colouring agent providing a metallic colour preferably being present in a pulverized state and/or in an amount of 10 - 80 wt% of said oil base.
  • the colouring agent is a colouring agent providing a silvery appearance, such as aluminium powder.
  • the colouring agent is a colouring agent providing a copper-like appearance, such as copper powder.
  • the colouring agent is a colouring agent providing a golden appearance, such as gold bronze powder.
  • the weight ratio of colouring agent:oil base may range from 0.01 :0.50, such as 0.02:0.45, e.g. 0.05:0.40, such as 0.10:0.35, such as 0.15:30, for example 0.20:0.25.
  • This example illustrates a method according to the first aspect of the present invention for the preparation of an oil base according to the second aspect of the present invention.
  • sandarac resin 350 g stand oil was provided along with 100 g sandarac resin and 200 g purified (bleached) beeswax. Before use, the sandarac resin was rinsed in ethanol and subsequently strained in a sieve.
  • the stand oil was poured into a pressure cooker and the sandarac resin and 5 ml of linseed oil varnish was added to the stand oil. This mixture was heated to approximately 30 °C until the sandarac resin was dissolved. Subsequently, the beeswax was added. This mixture was heated to approximately 30 °C in order to obtain a homogeneous mixture. The mixture was carefully stirred during the heating.
  • the temperature of the content of the pressure cooker was increased from 30 °C to 95 °C.
  • the temperature was kept at 95 °C for 4 hours whereafter the temperature was lowered to 60 °C.
  • the temperature was kept at 60 °C for 4 hours.
  • the mixture was subjected to a steam blowing process, wherein water steam was blown into the mixture obtained above.
  • the steam blowing took place for 10 seconds and was performed while the mixture was agitated.
  • the obtained mixture had a hazy, partly transparent white to slightly yellow appearance.
  • This example illustrates a method according to the first aspect of the present invention for the preparation of an oil base according to the second aspect of the present invention.
  • Example 3 The procedure as set out in respect of Example 1 above was repeated with the exception that no aluminium bronze was added prior to the steam blowing process.
  • This example illustrates a method according to the first aspect of the present invention for the preparation of an oil base according to the second aspect of the present invention.
  • Example 1 The procedure as set out in respect of Example 1 above was repeated with the exception that after addition of the aluminium bronze and prior to the steam blowing step, the mixture was poured into casting moulds. The mixture was allowed to rest for four weeks at room temperature in these moulds. Upon cooling to room temperature, the mixture solidified to a waxy product.
  • the waxy product was melted before the steam blowing process step.
  • This example illustrates the painting of a painting using traditional oil paints and using drying agents.
  • a canvas of Belgian linen suspended on a wooden frame measuring 50 x 50 cm was painted by blending traditional oil painting paints representing the full visible colour spectrum with siccative on a palette. After a drying time of 8 hours the applied layers of oil painting paints were dry enough for application of a new layer of paints. The evaporation of the solvents of the siccative left behind in the studio a heavy smell of organic solvents.
  • Example 5
  • This example illustrates the painting of a painting using traditional oil paints and where no siccative was used.
  • Example 4 was repeated with the exception that no siccative or other drying agents were used. In this case, the applied oil paints were not dry enough for application of a new layer of paint before even after a drying time of more than two months.
  • This example illustrates according to the fourth aspect of the present invention the preparation of a canvas comprising an oil base according to the second aspect of the present invention.
  • Example 7 accordingly illustrates the beneficial effect of an oil base according to the first aspect of the present invention allowing oil painting without use of hazardous solvents and drying agents.
  • This example illustrates the preparation of fast drying oil painting paints according to the fifth aspect of the present invention and comprising an oil base according to the second aspect of the present invention.
  • the weight ratio colour pigment:oil base ranged from 0.01 :0.50.
  • the oil painting paints were obtained by gradually blending and mixing in an amount of a specific pulverised colour pigment in a predetermined amount of oil base. An artist was allowed to paint a painting on a traditional oil painting canvas of
  • the artist was able to utilise the modelling effect of the oil paints and apply thick layers of paint onto the canvas where desired by not blending in any additional oil in the oil paints; or to apply thin, silk like layers where desired by blending in a small amount of bleached linseed oil into the oil paints.
  • the viscosity of the paints could be adjusted by adding bleached linseed oil.
  • the oil paints adhered very well to the canvas and the artist was able to easily smear out the paints on the canvas and onto the layer of paint already applied to the canvas.
  • the oil paints did not flow or drip or otherwise move, once applied to the canvas.
  • oil paints could be mixed with various kinds of additives, such as matting additives and glossing additives conventionally and traditionally used with oil paints for artistic use.
  • additives such as matting additives and glossing additives conventionally and traditionally used with oil paints for artistic use.
  • matting additives and glossing additives conventionally and traditionally used with oil paints for artistic use.
  • the same visual effects of the oil painting paints as with traditional oil paints could be obtained.
  • the oil paints of this example provided better possibilities of modelling the oil paints into thick layers and thereby to obtain an improved depth effect of the oil paints, compared to traditional oil paints.
  • This example illustrates the preparation of fast drying oil painting paints according to the fifth aspect of the present invention and comprising an oil base according to the second aspect of the present invention.
  • a same range of colour pigments in different colours as were used in Example 7 were each individually mixed with the oil base obtained in Example 2.
  • Oil bases according to the second aspect of the present invention made from the constituents set out in the table 1 below were made following the procedure set out in example 1 and 2 respectively:
  • oil bases of example 9a, 9b, 9c and 9d all showed similar behaviour as the oil bases obtained in example 1 and 2.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Paints Or Removers (AREA)

Abstract

Cette invention concerne un procédé de fabrication d'une base huileuse pour peintures à l'huile artistiques, ledit procédé impliquant les étapes suivantes : i) utiliser une certaine quantité de standolie ; ii) utiliser une certaine quantité de résines naturelles, lesdites résines comprenant au moins 10 % en poids de résine sandarac, de résine mastic ou d'un mélange de celles-ci, sur la base de la quantité totale des résines naturelles ; iii) utiliser une certaine quantité de cires naturelles, lesdites cires naturelles comprenant au moins 10 % en poids de cire d'abeilles, sur la base de la quantité totale des cires naturelles ; iv) mélanger ladite quantité de standolie préparée à l'étape i) avec ladite quantité de résines naturelles préparées à l'étape ii) et ladite quantité de cires naturelles préparées à l'étape iii) ; v) agiter avec précautions le mélange obtenu à l'étape iv) à une température qui permet d'obtenir un mélange homogène ; vi) refroidir éventuellement le mélange homogène obtenu à l'étape précédente jusqu'à la température ambiante ; vii) soumettre le mélange obtenu à l'étape précédente à un procédé d'étirage par soufflage par injection de vapeur dans ledit mélange pendant un laps de temps suffisant pour conférer un aspect brumeux audit mélange ; ledit procédé d'étirage par soufflage étant de préférence mis en œuvre sous agitation. Cette invention concerne en outre une base huileuse en soi ainsi que ses utilisations.
PCT/DK2011/000058 2011-06-09 2011-06-09 Base huileuse pour peintures à l'huile WO2012167786A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PCT/DK2011/000058 WO2012167786A1 (fr) 2011-06-09 2011-06-09 Base huileuse pour peintures à l'huile

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/DK2011/000058 WO2012167786A1 (fr) 2011-06-09 2011-06-09 Base huileuse pour peintures à l'huile

Publications (1)

Publication Number Publication Date
WO2012167786A1 true WO2012167786A1 (fr) 2012-12-13

Family

ID=44628777

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/DK2011/000058 WO2012167786A1 (fr) 2011-06-09 2011-06-09 Base huileuse pour peintures à l'huile

Country Status (1)

Country Link
WO (1) WO2012167786A1 (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104292919A (zh) * 2014-09-24 2015-01-21 安徽省中彩印务有限公司 一种亚光调色颜料
CN105950016A (zh) * 2016-05-31 2016-09-21 无锡伊佩克科技有限公司 一种钢铁用除锈防锈涂料及其制备方法
CN105950015A (zh) * 2016-05-26 2016-09-21 广西梧州龙鱼漆业有限公司 防蚊环保油漆
KR20190049158A (ko) * 2017-11-01 2019-05-09 장철영 도자기 복원용 접착제
CN110204913A (zh) * 2019-07-10 2019-09-06 湖州思源颜料有限公司 一种道路沥青氧化铁绿颜料的配方及制备方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB190917815A (en) * 1909-07-31 1910-05-05 Hudson Earle Improvements in "Primings" or Paints.
CN1097438A (zh) * 1993-07-12 1995-01-18 孙平 新型油画颜料及其制作方法
EP0652270A2 (fr) * 1993-11-08 1995-05-10 Auro Pflanzenchemie GmbH Composition de revêtement diluable à l'eau, translucide ou opaque
WO2000000551A1 (fr) * 1998-06-26 2000-01-06 Fels Donald C Jr Liant de peinture pour artistes
US7141109B1 (en) * 2004-06-03 2006-11-28 Velasquez Louis R Paint medium and method of production

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB190917815A (en) * 1909-07-31 1910-05-05 Hudson Earle Improvements in "Primings" or Paints.
CN1097438A (zh) * 1993-07-12 1995-01-18 孙平 新型油画颜料及其制作方法
EP0652270A2 (fr) * 1993-11-08 1995-05-10 Auro Pflanzenchemie GmbH Composition de revêtement diluable à l'eau, translucide ou opaque
WO2000000551A1 (fr) * 1998-06-26 2000-01-06 Fels Donald C Jr Liant de peinture pour artistes
US7141109B1 (en) * 2004-06-03 2006-11-28 Velasquez Louis R Paint medium and method of production

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
ANONYMOUS: "Paul McMillan -Biographical Statement", 18 July 2003 (2003-07-18), XP002659887, Retrieved from the Internet <URL:http://web.archive.org/web/20030718193828/http://www.paulmcmillan.com/biography.html> [retrieved on 20110923] *
DATABASE WPI Week 199719, Derwent World Patents Index; AN 1997-204160, XP002659886 *
PITTHARD V ET AL: "Gas Chromatography - Mass Spectrometry of Binding Media from Early 20th Century Paint Samples from Arnold Schönberg's Palette", CHROMATOGRAPHIA ; AN INTERNATIONAL JOURNAL FOR RAPID COMMUNICATION IN CHROMATOGRAPHY, ELECTROPHORESIS AND ASSOCIATED TECHNIQUES, VIEWEG VERLAG, WI, vol. 62, no. 3-4, 1 August 2005 (2005-08-01), pages 175 - 182, XP019358484, ISSN: 1612-1112 *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104292919A (zh) * 2014-09-24 2015-01-21 安徽省中彩印务有限公司 一种亚光调色颜料
CN104292919B (zh) * 2014-09-24 2016-08-24 安徽省中彩印务有限公司 一种亚光调色颜料
CN105950015A (zh) * 2016-05-26 2016-09-21 广西梧州龙鱼漆业有限公司 防蚊环保油漆
CN105950016A (zh) * 2016-05-31 2016-09-21 无锡伊佩克科技有限公司 一种钢铁用除锈防锈涂料及其制备方法
KR20190049158A (ko) * 2017-11-01 2019-05-09 장철영 도자기 복원용 접착제
KR102026372B1 (ko) 2017-11-01 2019-09-27 장철영 도자기 복원용 접착제
CN110204913A (zh) * 2019-07-10 2019-09-06 湖州思源颜料有限公司 一种道路沥青氧化铁绿颜料的配方及制备方法

Similar Documents

Publication Publication Date Title
WO2012167786A1 (fr) Base huileuse pour peintures à l&#39;huile
EP1741455B1 (fr) Ciment osseux coloré à base de polyméthyl méthacrylate et son procédé de préparation
US9062215B2 (en) Paint binder composition
KR101934526B1 (ko) 초기 착색력이 우수하고 점도 조절이 용이한 필오프 타입 눈썹 문신용 화장료 조성물
de Viguerie et al. Historical evolution of oil painting media: A rheological study
Vizárová et al. Stability studies of materials applied in the restoration of a baroque oil painting
Hendy et al. The ground in pictures
WO2015194936A1 (fr) Composition de cire à base d&#39;huile de palme
CN103436135A (zh) 高着色性油漆及其应用
De Viguerie et al. New insights on the glaze technique through reconstruction of old glaze medium formulations
JP2019001735A (ja) 固形粉末化粧料
Bestetti et al. Materials and methods for the self-production of retouching colours
US6011097A (en) Painting medium for artists
JP5103503B2 (ja) 食器又は箸用塗料組成物、食器・箸及びそれらの製造方法
CN101884349A (zh) 一种果蔬保鲜涂膜果蜡
US2594273A (en) Pasty vehicle for artist&#39;s paint
EP1730245B1 (fr) Emulsion a base de standolies d&#39;huiles vegetales ou animales et d&#39;emulsifiants naturels
US5623048A (en) Clear amber-based varnish and production thereof
Ferrer Altered Blue and Red paints: Investigations of Old Man in Warnemünde and The Drowned Boy by Edvard Munch (1863-1944)
US20040231562A1 (en) Gelled carrier composition for surface colorants and associated methods of use
JP5028336B2 (ja) 塗料組成物及びその製造方法
JP2008031367A (ja) 液状描画材
US20200123404A1 (en) Oil paint additive compositions
KR100897448B1 (ko) 인조 진주를 제조하기 위한 도장용 조성물 및 도장방법
JP2005213151A (ja) 自己調色ネイルエナメル

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: 11733988

Country of ref document: EP

Kind code of ref document: A1

122 Ep: pct application non-entry in european phase

Ref document number: 11733988

Country of ref document: EP

Kind code of ref document: A1