Patent Application
20210380796
The present invention relates to a polymeric composition suitable for injection molding comprising polymeric particles and a colorant.
In particular the present invention relates to a polymeric (meth)acrylic composition comprising polymeric particles and a mixture of colorants suitable for injection moulded compounds with high gloss.
The present invention concerns also the use of such a polymeric composition or polymeric (meth)acrylic composition comprising polymeric particles and a mixture of colorants in lightning applications and in injection molding.
The present invention concerns also a process for making a polymeric composition or (meth)acrylic composition comprising polymeric particles and a mixture of colorants suitable for injection moulded compounds with high gloss surface.
Thermoplastic polymers and especially (meth)acrylic polymers are widely used, including lightning applications. This is mainly due to its characteristics as a highly transparent polymer material with excellent resistance to ultraviolet radiation and weathering. So (meth)acrylic polymers are used for example in lamps, luminaires, light covers, displays, lit shelving, surfaces and illuminated signs.
The lightning applications have various requests on the (meth)acrylic polymers or the compositions based on (meth)acrylic polymers as light transmission, diffusing power. These compositions based on (meth)acrylic polymers comprise generally more or less spherical particles, which are also polymeric particles or other organic particles or inorganic particles.
Additionally it is of also of great interest to have a polymeric composition with a good compromise between light transmission and diffusing properties and having glossy surface appearance, hiding the light source and that the light or coloured light is transmitted and diffused when the light source is switched on. Last point is especially important for lightning applications where it is for example required that a sign is to be visible in the daytime when the light source is off or not necessarily switched on; but also at night, or in half-darkness, when the light source is switched on.
This compromise is based on the correct or optimal quantity of the respective particles and its particle size in the polymeric composition and colorants in the polymeric composition.
Therefore it is important to have a polymeric composition that contains polymeric particles and colorants that can be used in lightning devices that comprises LEDs that can hide the light source and that light or coloured light is transmitted and diffused when the light source is switched on. The surface of the transformed polymer composition should be very glossy and obtained in a simple process.
The objective of the present invention is to provide a polymeric composition comprising polymeric particles and colorants suitable for lightning applications having a highly glossy surface.
An additional objective of the present invention is to provide a polymeric composition comprising polymeric particles and colorants for lightning applications giving an aspect contrast and/or color contrast independent of the color of lightning source by using the same polymeric composition and having a highly glossy surface.
Another objective of the present invention is to provide a polymeric composition comprising polymeric particles and colorants, so that the composition, when used in a lightning application as a cover and the light source is lit on, the lightning device comprising said composition as cover can transmit light over the whole range of wavelength of visible light and possesses a highly glossy surface.
Again still another objective of the present invention is to provide a luminous device comprising a light source and a polymeric composition comprising polymeric particles and colorants as cover of the light source, that when the light source is lit on, it is hidden and can transmit light over the whole range of wavelength of visible light and the cover possesses a highly glossy surface.
The diffusion of light which increases the relative diffusion power and the hiding power is usually increased by adding scattering particles to the composition.
The document EP 1864274 discloses an illuminating device combining a LED and a diffusing sheet. The luminous device comprises at least one light-emitting diode and at least one cover made of a transparent plastic in which particles that scatter the light emitted by the light-emitting diode are dispersed.
The document EP 1927098 discloses an illuminating device combining a white LED and a diffusing sheet. The luminous device comprises at least one white light-emitting diode and at least one cover made of a transparent plastic in which particles that scatter the light emitted by the light-emitting diode are dispersed
The document US 2016/0245954 discloses an optical diffusion blend material for LED lightning. The diffusing blend comprises a mixture of inorganic particles and organic particles.
The document WO2004/098857 discloses an injection molding method for the production of light diffusing molded items. The molding material comprises a matrix of polymethyl methacrylate and spherical plastic particles with a particle size of 1 to 24 μm.
The prior art does not discloses polymeric compositions comprising polymeric particles and a mixture of colorants at the same time, suitable for lightning applications or luminous devices comprising polymeric compositions that can hide the light source and that light or coloured light is transmitted and diffused when the light source is switched on, while possessing a very glossy surface.
Surprisingly it has been discovered that a polymeric composition PC1 comprising:
Surprisingly it has been discovered that a polymeric composition PC1 comprising:
Surprisingly it has been discovered that a polymeric composition PC1 comprising:
It has also been found that a process for obtaining a polymeric composition PC1, said composition PC1 comprises:
According to a first aspect, the present invention relates to a polymeric composition PC1 comprising:
According to a second aspect, the present invention relates to a polymeric composition PC1 comprising:
According to a third aspect, the present invention relates to a process for manufacturing a polymeric composition PC1, said composition PC1 comprises:
According to a fourth aspect, the present invention relates to the use of a polymeric composition PC1 comprising:
According to a fifth aspect, the present invention relates to a lightning device comprising a polymeric composition PC1 comprising:
According to still another aspect the present invention relates to a process for manufacturing a lightning device, said process comprises the steps of:
By the term “alkyl(meth)acrylate” as used is denoted to both alkyl acrylate and alkyl methacrylate.
By the term “copolymer” as used is denoted that the polymers consists of at least two different monomers.
By the term “parts” as used herein is denoted “parts by weight”.
By the term “thermoplastic polymer” as used is denoted a polymer that turns to a liquid or becomes more liquid or less viscous when heated and that can take on new shapes by the application of heat and pressure.
By the term “(meth)acrylic polymer” as used in the present invention is denoted a polymer with weight ratio of acrylic or methacrylic monomers inside the (meth)acrylic polymer of at least 50 wt %.
By the term “PMMA” as used in the present invention are denoted homo- or copolymers of methyl methacrylate (MMA), for the copolymer of MMA the weight ratio of MMA inside the PMMA is at least 50 wt %.
By the term “masterbatch” as used is understood composition that comprises an additive in high concentration in a carrier material. The additive is dispersed in the carrier material.
By the term “high gloss” as used is understood that the gloss measure according to ASTM D523 at 60° is more than 70GU, preferably more than 75GU and advantageously more than 80GU.
By saying that a range from x to y in the present invention, it is meant that the upper and lower limit of this range are included, equivalent to at least x and up to y.
By saying that a range is between x and y in the present invention, it is meant that the upper and lower limit of this range are excluded, equivalent to more than x and less then y.
With regard to the polymeric composition PC1 according to the invention it comprises a polymer P1, polymeric particles PP1 having a weight average particle diameter between 0.5 μm and 20 μm and colorants CA1 to CAn characterized in that the colorant is mixture of colorants CA1 to CAn with n>1 in the composition PC1. In other words there are at least two different colorants CA1 and CA2 in the polymeric composition PC1.
The polymer P1 is chosen from can be chosen from (meth) acrylic polymers, polycarbonate, polystyrenes, polyesters, polyvinylchloride (PCV), cyclic olefin copolymers, styrene methyl methacrylate (SMMA), styrene acrylonitrile (SAN), polyvinylidene fluoride (PVDF) and blends thereof.
Preferably the polymer P1 is chosen from (meth) acrylic polymers, so that the polymer P1 is a (meth)acrylic polymer AP1.
In a first preferred embodiment the polymeric composition PC1 comprises a) a (meth)acrylic polymer AP1, b) polymeric particles PP1 having a weight average particle diameter between 0.5 μm and 20 μm and c) colorants CA1 to CAn, is characterized in that the particle PP1 represents between 0.05 wt % and 50 wt % of the polymeric composition PC1 comprising the components a), b) and c). However the weight ratios of the particles of component b) is calculated on the sum of the two components a) and b) only. More preferred according to the first preferred embodiment, the particle PP1 represents between 0.06 wt % and 40 wt %, still more preferred between 0.075 wt % and 30 wt % and advantageously between 0.1 wt % and 20 wt % of the composition PC1 calculated on the sum of the two components a) and b) only.
The light transmission for a composition comprising a) and b) for a sheet of 3 mm thickness is at least 80%. The light transmission is measured according to the norm ASTM D1003.
In a second preferred embodiment the polymeric composition PC1 comprises at least one additional colorant CB, which if different from any of the colorants CA1 to CAn already present in the polymeric composition PC1.
In a third preferred embodiment the polymeric composition PC1 comprises a) a (meth)acrylic polymer AP1, b) polymeric particles PP1 having a weight average particle diameter between 0.5 μm and 20 μm and c) colorants CA1 to CAn and at least one additional colorant CB, which if different from any of the colorants CA1 to CAn already present in the polymeric composition PC1, is characterized in that the particle PP1 represents between 0.05 wt % and 50 wt % of the polymeric composition PC1 comprising the components a), b) and c) is calculated on the sum of the two components a) and b) only.
With regard to the (meth)acrylic polymer AP1 it is a (meth)acrylic block copolymer MBC or a (meth)acrylic polymer MP1.
In a first preferred embodiment the (meth)acrylic polymer AP1 is a (meth)acrylic polymer composition MP1.
The (meth)acrylic polymer composition MP1 comprises a polymeric polymer chain comprising at least 50 wt % of monomers coming acrylic and/or methacrylic monomers. The (meth)acrylic polymer could also be a mixture of two or more (meth)acrylic polymers MP1 to MPx.
The acrylic and/or methacrylic monomers are chosen from acrylic acid, methacrylic acid, esters of acrylic acid of esters of methacrylic acid, alkyl acrylic monomers, alkyl methacrylic monomers and mixtures thereof.
Preferably the monomer is chosen from acrylic acid, methacrylic acid, alkyl acrylic monomers, alkyl methacrylic monomers and mixtures thereof, the alkyl group having from 1 to 22 carbons, either linear, branched or cyclic; preferably the alkyl group having from 1 to 12 carbons, either linear, branched or cyclic.
Advantageously the meth)acrylic monomer is chosen from methyl methacrylate, ethyl methacrylate, methyl acrylate, ethyl acrylate, methacrylic acid, acrylic acid, n-butyl acrylate, iso-butyl acrylate, n-butyl methacrylate, iso-butyl methacrylate, cyclohexyl acrylate, cyclohexyl methacrylate, isobornyl acrylate, isobornyl methacrylate and mixtures thereof.
Other comonomers can be copolymerized with the acrylic and/or methacrylic monomers as long as the (meth)acrylic polymer AP1 is comprising at least 50 wt % of monomers coming acrylic and/or methacrylic monomers in its polymeric chain. The other comonomers can be chosen from styrenic monomers as styrene or styrene deriviatives, acrylonitrile, vinylesters as vinylacetate. The amount of these comonomers is from 0 wt % to 50 wt %, preferably from 0 wt % to 40 wt %, more preferably from 0 wt % to 30 wt %, advantageously from 0 wt % to 20 wt %.
In a first preferred embodiment the (meth)acrylic polymer composition MP1 is a homo- or copolymer of methyl methacrylate (MMA) that comprises at least 50%, preferably at least 60%, advantageously at least 70% and more advantageously at least 80% by weight of methyl methacrylate.
The copolymer of methyl methacrylate (MMA) comprises between 50% and 99.9% by weight of methyl methacrylate and between 0.1 and 50% by weight of at least one monomer having at least one ethylenic unsaturation that can copolymerize with methyl methacrylate.
These monomers are well known and mention may be made, in particular of acrylic and methacrylic acids and alkyl-(meth)acrylates in which the alkyl group has from 1 to 12 carbon atoms. As examples, mention may be made of methyl acrylate and ethyl, butyl or 2-ethylhexyl (meth)acrylate. Preferably the comonomer is an alkyl acrylate in which the alkyl group having from 1 to 4 carbon atoms.
According to the first more preferred embodiment the copolymer of methyl methacrylate (MMA) comprises from 80% to 99.8% advantageously from 90% to 99.7% and more advantageously from 90% to 99.5% by weight of methyl methacrylate and from 0.2% to 20% advantageously from 0.3% to 10% and more advantageously from 0.5% to 10% by weight of at least one monomer having at least one ethylenic unsaturation that can copolymerize with methyl methacrylate. Preferably the comonomer is chosen from methyl acrylate or ethyl acrylate or mixtures thereof.
The (meth)acrylic polymer composition MP1 has a melt flow index (MFI) according to ISO 1133 (230° C./3.8 kg) between 0.1 g/10 min and 20 g/10 min. Preferably melt flow index is between 0.2 g/10 min and 18 g/10 min, more preferably between 0.3 g/10 min and 16 g/10 min, advantageously between 0.4 g/10 min and 13 g/10 min.
The (meth)acrylic polymer composition MP1 has a refractive index between 1.46 and 1.52, preferably between 1.47 and 1.52 and more preferably between 1.48 and 1.52.
The (meth)acrylic polymer composition MP1 has a light transmittance according to ASTM D-1003 (sheet of 3 mm thickness) of at least 85%, preferably 86%, more preferably 87%.
The (meth)acrylic polymer composition MP1 has a Vicat softening temperature of at least 90° C. The Vicat softening temperature is measured according to ISO 306:2013 (B50 method).
The composition according to the invention can comprise beside the (meth)acrylic polymer MP1 also an (meth)acrylic polymer MP2. The (meth)acrylic polymer MP1 and (meth)acrylic polymer MP2 form a mixture or a blend. This mixture or blend consists of at least one homopolymer and at least one copolymer of MMA, or a mixture of at least two homopolymers or two copolymers of MMA with a different average molecular weight or a mixture of at least two copolymers of MMA with a different monomer composition.
According to a second preferred embodiment the (meth)acrylic polymer AP1 it is a (meth)acrylic block copolymer MBC.
The (meth)acrylic block copolymer MBC comprises at least one block having a glass transition temperature less than 20° C. preferably less than 10° C. more preferably less than 0° C., advantageously less than −5° C. and more advantageously less than −10° C.
Preferably (meth)acrylic block copolymer MBC comprises at least one block which is an (meth)acrylic block. By this is meant that at least 50 wt % of the monomers inside this block are alkyl (meth)acrylate monomers, that have been polymerized.
Most preferably the (meth)acrylic block copolymer MBC comprises least 50 wt % of the monomers inside (meth)acrylic block copolymer MBC are alkyl(meth)acrylate monomers, that have been polymerized.
The (meth)acrylic block copolymer MBC is having a general formula (A)nB in which:
Advantageously the (meth)acrylic block copolymer MBC is amorphous.
Preferably, in the block A the monomer is chosen from methyl methacrylate (MMA), phenyl methacrylate, benzyl methacrylate, isobornyl methacrylate, styrene (Sty) or alpha-methylstyrene or mixtures thereof. More preferably, the block A is PMMA or PMMA copolymerized with acrylic or methacrylic comonomers or polystyrene (PS) or PS modified with styrenic comonomers.
Preferably the block B comprises monomers chosen of methyl acrylate, ethyl acrylate, butyl acrylate (BuA), ethylhexyl acrylate or butyl methacrylate and mixtures thereof, more preferably butyl acrylate said monomers make up at least 50 wt %, preferably 70 wt % of block B.
Furthermore, the blocks A and/or B can comprise other acrylic or methacrylic comonomers carrying various chemical function groups known to a person skilled in the art, for example acid, amide, amine, hydroxyl, epoxy or alkoxy functional groups. The block A can incorporate groups, such as acrylic acid or methacrylic acid (MAA), in order to increase the temperature stability of thereof.
Comonomers like styrene can also be incorporated in the block B in order to mismatch the refractive index of the block A.
Preferably, said thermoplastic acrylic block copolymer has a structure chosen from: ABA, AB, A3B and A4B.
The (meth)acrylic block copolymer MBC for example can be one of the following triblock copolymers: pMMA-pBuA-pMMA, p(MMAcoMAA)-pBuA-p(MMAcoMAA), p(MMAcoMAA)-p(BuAcoSty)-p(MMAcoMAA) and p(MMAcoAA)-pBuA-p(MMAcoAA). In a first preferred embodiment, the (meth)acrylic block copolymer MBC is p(MMAcoMAA)-p(BuAcoSty)-p(MMAcoMAA).
It is known to a person skilled in the art that the polymers of PMMA type can comprise small amounts of acrylate comonomer in order to improve the temperature stability thereof. By small is meant less than 9 wt %, preferably less than 7 wt % and more preferably less than 6 wt % of the polymer.
The block B represents from 10% to 85%, preferably 15% to 80% of the total weight of the block copolymer MBC.
The block B has a weight-average molar mass of between 10 000 g/mol and 500 000 g/mol, preferably from 20 000 g/mol to 300 000 g/mol. The weight average molar mass can be measured by size exclusion chromatography (SEC).
The (meth)acrylic block copolymers can be obtained by controlled radical polymerization (CRP) or by anionic polymerization; the most suitable process according to the type of copolymer to be manufactured will be chosen.
Preferably, this will be CRP, in particular in the presence of nitroxides, for the (meth)acrylic block copolymers of (A)nB type and anionic or nitroxide radical polymerization, for the structures of ABA type, such as the triblock copolymer MAM. Controlled radical polymerization is described in the document for obtaining block copolymers, i.e. in WO03/062293.
The (meth)acrylic block copolymer MBC can be transformed by extrusion or injection molding in form of a object.
According to a third preferred embodiment the (meth)acrylic polymer AP1 it is a blend of a (meth)acrylic block copolymer MBC with a (meth)acrylic polymer MP1.
With regard to the polymeric particles PP1, it is having a weight average particle diameter between 0.5 μm and 20 μm, preferably a weight average particle diameter between 1 μm and 19 μm, more preferably between 1 μm and 18 μm, advantageously between 1 μm and 17 μm and most advantageously between 1 μm and 15 μm.
The polymeric particle PP1 can also be a mixture of different kind of particles. Either it can be particles of the same chemical nature having a different weight average particle diameter, as long as both are within the interval between 0.5 μm and 20 μm for weight average particle diameter. Or it can be particles of different chemical nature having the same or a different weight average particle diameter, as long as both are within the interval between 0.5 μm and 20 μm for the weight average particle diameter.
With regard to the polymeric particles PP1 they can be chosen from silicone particles, (meth)acrylic particles, styrenic particles and mixtures thereof. The particles can be crosslinked or partly crosslinked. The polymeric particles PP1 can be mixtures of different kind of particles.
With regard to polymeric silicone particle as polymeric particles PP1, it is having a weight average particle diameter between 0.5 μm and 20 μm.
In a first preferred embodiment the silicone particles PP1 comprises polysiloxanes chains having a silicone-oxygen backbone chain.
The polymeric silicone particle PP1 has a refractive index between 1.30 and 1.45, preferably between 1.35 and 1.45, advantageously between 1.36 and 1.44.
In a first preferred embodiment the weight average particle diameter of the polymeric silicone particle PP1 is preferably between 1 μm and 15 μm, more preferably between 1 μm and 8 μm, still more preferably between 1 μm and 7 μm, even more preferably between 1 μm and 6 μm, advantageously between 1 μm and 5 μm and more advantageously between 1 μm and 4 μm.
The bulk density of a powder of the polymeric silicone particle PP1 is between 0.1 g/ml and 0.5 g/ml, preferably between 0.15 and 0.47 g/ml.
The polymeric silicone particle PP1 can for example be prepared according to US 2008/124549.
The polymeric silicone particle could also be a blend of two or more different silicone particles PP1a, PP1b . . . , as long as all silicone particles have the before mentioned characteristics.
In this first preferred embodiment if the polymeric particle PP1 is polymeric silicone particle, the polymeric particle PP1 represents between 0.06 wt % and 10 wt %, still more preferred between 0.075 wt % and 5 wt % and advantageously between 0.1 wt % and 3 wt % of the composition PC1 calculated on the sum of the two components a) and b) only
Commercial available silicon particles are from ShinEtsu Silicone powder KMP series as for example KMP-600 or KMP-601, from DOW CORNING for example 30-424 additive silicone powder, from MOMENTIVE Tospearl series as for example Tospearl20, Tsopearl30 or Tospearl240.
With regard to polymeric (meth)acrylic particles as polymeric particles PP1, they are having a weight average particle diameter between 1 μm and 20 μm, it comprises at least 50 wt % of monomers coming from acrylic and/or methacrylic monomers in the polymer chains of the polymeric particle PP1.
In a first preferred embodiment the polymeric (meth)acrylic particle PP1 is a homo- or copolymer of methyl methacrylate (MMA) that comprises at least 50%, preferably at least 60%, advantageously at least 65% and more advantageously at least 70% by weight of methyl methacrylate.
The weight average particle diameter of the polymeric (meth)acrylic particle PP1 is preferably between 1 μm and 19 μm, more preferably between 2 μm and 15 μm and advantageously between 2 μm and 10 μm.
Preferably the polymeric (meth)acrylic particle PP1 is crosslinked. The weight ratio of the crosslinker in the (meth)acrylic particle PP1 is less than 5 wt %. The crosslinker is preferably chosen from an organic compound having at least one acrylic or methacrylic function and a second double bond which can polymerize as well.
The polymeric (meth)acrylic particle PP1 has a refractive index between 1.49 and 1.56, preferably between 1.50 and 1.55.
The polymeric (meth)acrylic particle PP1 can be prepared according to suspension polymerization.
The polymeric (meth)acrylic particle could also be a blend of two or more different (meth)acrylic particles PP1a, PP1b . . . , as long as all particles have the before mentioned characteristics.
The polymeric composition PC1 according to the invention does not comprise polymeric particles having a weight average particle diameter larger than 20 μm. For being clear the polymeric particle PP1 having a weight average particle diameter between 0.5 μm and 20 μm, can have due to the distribution of particles sizes a certain percentage of particles that are larger than 20 μm. However the weight average particle diameter polymeric particle PP1 is less than 20 μm and there is not another population of other particles in the composition PC1 having a weight average particle diameter larger than 20 μm. This applies also for mixtures of different particles, if there is a mixture of particles, all weight average particle diameters are less than 20 μm.
In a first preferred embodiment the polymeric particle PP1 is chosen from silicone particles.
With regard to the colorants CA or CA1 to CAn, it can be a pigment or a dye or a mixture of pigments and dyes. The pigment can be an inorganic pigment or an organic pigment.
In a first preferred embodiment the colorants CA or CA1 to CAn is a mixture of pigments and dyes.
In a second preferred embodiment the colorants CA or CA1 to CAn is a mixture of dyes.
In a third preferred embodiment the colorants CA or CA1 to CAn is a mixture of pigments.
The colorants CA is mixture of colorants CA1 to CAn with n>1. Preferably the value n is 1<n<10 and more preferably 1<n<9 More preferably n is a natural number.
In a first even more preferred embodiment the value n is 1<n<8.
In a second even more preferred embodiment the value n is 2<n<9.
In a third even more preferred embodiment the value n is 2<n<8.
In a fourth even more preferred embodiment the value n is 1<n<6.
In a fifth even more preferred embodiment the value n is 2<n<6.
The colorants CA1 to CAn are chosen that one colorant CA1 is red or yellow or orange or green or blue or violet, and that the other colorant CA2 is red or yellow or orange or green or blue or violet but has a different colour than the colorant CA1; and that the possible still another colorant CA3 is red or yellow or orange or green or blue or violet but has a different colour than the colorant CA1 and CA2; and so on until colorant CAn.
In a first preferred embodiment, the colorants CA1 to CAn are having all a different color
The mixture of colorants CA1 to CAn is preferably yielding to grey color. The mixture of colorants CA1 to CAn is preferably having following values 20<L*<80, −20<a*<20, −20<b*<20, more preferably 30<L*<70, −10<a*<10, −10<b*<10, still more preferably 30<L*<70, −5<a*<5, −5<b*<5.
The three values L, a*, b* are used to characterize the principal color in the CIELAB system. L denotes the luminosity and extends from 0 (black) to 100 (white). The value a* measures the red and green of the color: the colors tending toward green have a negative value while those tending toward the red have a positive a* value. The b* value measures the blue and the yellow of the color: colors tending toward the yellow have a positive b* value while those tending toward the blue have a negative b* value. The L, a*, b* values are measured using a spectrum colorimeter (especially according to the ASTM E 308 standard).
The mixture of colorants CA1 to CAn is chosen that, when blended with a transparent material as polymer P1, a sheet made of transparent material with colorants absorbs in a homogenous way over the whole spectrum of visible light between 400 nm and 700 nm. By homogenous is meant that the variation of the light transmission is small and varies only in an interval of less than 30% of absolute value. Preferably this variation is less than 25% and advantageously less than 20%. This is shown in
Preferably the light transmission is between 5% and 40%, more preferably between 10% and 30% in a wavelength interval of 400 nm-700 nm for a sheet of (meth)acrylic polymer AP1 having 2 mm thickness comprising colorants CA1 to CAn.
Colorants for polymers are known and can be for example chosen from the product lines of the companies Lanxess, Clariant, Synthesia or BASF for pigments and dyes. There are the MACROLEX® dyes from Lanxess as Yellow 6G Gran, Yellow 3G Gran, Yellow G Gran, Yellow E2R Gran, Orange 3G Gran, Orange R Gran, Red E2G Gran, Red A, Red EG Gran, Red B, Red 5B Gran, Violet, 3R Gran, Violet B Gran, Blue 3R, Blue RR Gran, Green 5B Gran and Green G. There are the Solvaperm® dyes and Polysynthren® polymer colorants from Clariant as Yellow 3G, Yellow 2G, Orange 3G, Red 2G, Red G, RED PFS, RED BB, Red Violet R, Violet RSB, Blue 2B, Green, GSB, Green G, Yellow GG, Yellow NG, Red GFP, Violet G, Blue R, Blue RLS, Brown 3RL and Brown R.
The colorants are for example derivatives of methane, pyrazolone, quinophtalone, perinone, azo, anthraquinone, coumarine
The colorants can be for example:
The quantity of the colorants CA1 to CAn in the polymeric composition PC1, is between 10 weight ppm and 10 000 weight ppm relative to the polymer P1, preferably between 20 weight ppm and 8000 weight ppm, more preferably between 50 weight ppm and 5000 weight ppm. The quantity of the respective colorants is chosen so that mixture of colorants CA1 to CAn is preferably has a grey color, as defined before and that the mixture of colorants CA1 to CAn when blended with a transparent material as polymer P1, a sheet made out of transparent material with colorants absorbs in a homogenous way over the whole spectrum of visible light between 400 nm and 700 nm, as also defined before.
The quantity of the colorant is chosen on function of its relative colour (tinting) strength. This value can be found in commercial brochures or material data sheets (according to DIN 53235 and expressed in SD1/3-reduced shade to international standard depth 1/3).
With regard to the colorants CB, of the second preferred embodiment the polymeric composition PC1 or the third preferred embodiment the polymeric composition PC1, it can be a pigment or a dye or a mixture of pigments and dyes. The pigment can be an inorganic pigment or an organic pigment. The colorant CB can be chosen from the same colorants as the colorants CA1 to CAn.
With regard to the process for the preparation a polymeric composition PC1 according to the invention, it comprises the steps of providing and blending the components a), b) and c).
More particularly process for manufacturing a polymeric composition PC1, said composition PC1 comprises:
The blending can be made in any order: that the compound b) is added first to compound a) and afterward compound c) is added, or that compound c) is added first to compound a) and afterward compound b), or that compound b) and c) are added together at the same time.
Optionally the colorant CB is added.
Preferably the blending step ii) of the process is made by compounding or mixing.
The components a), b) and c) and their preferred embodiments are the same as defined before.
Said process for the manufacturing the polymeric composition PC1 uses preferably a masterbatch or liquid colour of colorants CA1 to CAn. The masterbatch or liquid colour comprises between 100 ppm by weight and 50% by weight of colorants.
In a first preferred embodiment of the process for the preparation a polymeric composition PC1 a masterbatch is used.
In a second preferred embodiment for the preparation a polymeric composition PC1 a liquid color is used. An example for liquid color concentrates is given in the document US2009/0156732.
According to a further aspect the present invention concerns a process for making an object by transforming and/or processing the polymeric composition PC1 according to the invention.
The transformation can be made by injection molding, coinjection, injection molding combined with surface molding, extrusion, coextrusion or extrusion/blow molding. Preferably the transformation is made by injection moulding or extrusion. Advantageously the transformation is made by injection moulding.
The transformation process has no influence on the luminous effect of the polymeric composition comprising polymeric particles and colorants namely the aspect contrast and/or color contrast which independent of the color of lightning source by using the same polymeric composition.
In a first preferred embodiment of the process for making an object is made by injection moulding. A moulded object is obtained.
The process for making a moulded object according to the invention comprises the steps of
According to a still further aspect the present invention concerns the use of the polymeric composition PC1 for making an object or a moulded object.
The composition PC1 according to the invention can be used for making an object or a moulded object or article or be used to be part of an article. Preferably the object or a moulded object or article or be used to be part of an article made out of the composition according to the invention has a thickness of more than 50 μm, more preferably more than 100 μm and even more preferably more than 500 μm.
The composition PC1 obtained by the process according to the invention can be used to be transformed directly into an article or object or can be part of an article or object.
According to a still further aspect the present invention concerns an object or a moulded object made of the polymeric composition PC1 according to the present invention.
The object or moulded object of the invention can be in form of a sheet, block, film, tube or profiled element. Preferably the moulded objects a sheet, which can be plain or slightly bent or curved.
Examples for object or molded objects or articles are covers or plates for luminous devices.
In one embodiment the molded object is a cover for a light source. The cover generally has a thickness of between 0.001 cm and 15 cm, preferably between 0.01 cm and 10 cm, more preferably between 0.05 cm and 7 cm, more preferably between 0.1 cm and 5 cm and even more preferably between 0.2 cm and 4 cm.
Additionally according to another aspect of the present invention the composition obtained from the polymeric composition PC1 according to the invention can used as a covering for a point light source. The light source plus cover forms a lightning device. The cover may be a single layer, or may be a multi-layer structure. The cover is separated from the light source by a distance of between 0.1 cm and 50 cm, preferably between lcm and 40 cm, preferably between 2 cm and 20 cm and even more preferably between 3 cm and 20 cm.
In still another embodiment a lightning device comprises the polymeric composition PC1 according to the invention.
The luminous device or lightning device comprises a light source. Preferably the light source is a LED. The light source can be a white or a coloured LED.
For a lightning device comprising a polymeric composition PC1 according to the first preferred embodiment of composition PC1, the light source can be a white or a coloured.
For a lightning device comprising a polymeric composition PC1 according to the second or third preferred embodiment of composition PC1, the light source is preferably a white light source.
The lightning device according to the invention has a variety of applications such as, for example:
The optical properties of the polymers are measured according to following method: light transmittance and haze are measured according to the standard ASTM D1003, sheets of 2 mm thickness for molded samples. A haze-gard plus apparatus from BYK-Gardner is used. The gloss is measured according to ASTM D523.
Refractive index is measured with a refractometer.
Particle size: the particle diameter is measured by Laser diffraction with a Coulter Counter.
The three values L, a*, b* are measured by color spectrometry by reflection if the light source is off and by transmission if the light source is lit on. A color spectrometer “Color Sphere” from BYK-Gardner is used.
A copolymer of methyl methacrylate having a melt flow index of 8 g/10 min is used as (meth)acrylic polymer AP1a and a copolymer of methyl methacrylate having a melt flow index of 2.8 g/10 min is used as (meth)acrylic polymer AP1b, both as polymer P1.
As a first polymeric particle PP1a, DC30-424 silicone particles form DOW are used. The weight average particle diameter is between 1 μm and 3 μm and a batch having a weight average particle diameter of 2 μm was used.
As a second polymeric particle PP1b Paraloid EXL5137 from the company Röhm and Haas is used. The weight average particle diameter is between 4 μm and 6 μm and a batch having a weight average particle diameter of 5 μm was used.
As a comparative polymeric particle the (meth)acrylic particle MP1a in the comparative examples is used. The commercial product from ALTUGLAS BS110 having generally a weight average particle diameter between 35 μm and 60 μm and a batch having a weight average particle diameter of 50 μm was used.
Colorants: the colorants are added in form of masterbatches: MBgris and MB Red 18242. The MBgris is a masterbatch having a grey color comprising three colorants CA1 to CA1.
Colorant CA1: Red Solvent 135 from BASF, CAS [20749-68-2], 8,9,10,11-tetrachloro-12 h-phthaloperin-12-one
Colorant CA2: Solvent Green 28 from BASF, CAS [28198-05-2], 1,4-bis[(4-butylphenyl)amino]-5,8-dihydroxy-anthracene-9,10-dione
Colorant CA3: Violet solvent 13, CAS [81-48-3], 1-hydroxy-4-(p-tolylamino)anthracene-9,10-dione
The colorants CA1 to CA3 are blended together in a masterbatch MB1 at a weight level of 2500 ppm total colorants. This masterbatch MB1 is grey and if blended with a (meth)acrylic polymer AP1a or AP1b only at 3.7 phr, a sheet of 3 mm thickness has a light transmission between 10% and 20% over the wavelength interval of 400 nm-700 nm. This is shown in
Example 1 and 2 have the composition given in table 1 blended with 3.7 phr of the grey masterbatch MB1 for example 1 and 5.55 phr for example 2. Comparative examples 1 and 2 have the composition given in table 1 blended with 3.7 phr of the grey masterbatch MB1.
i) Ex = Example, CEx = Comparative Example
The compositions of the respective samples are transformed to sheets 100 mm*100 mm and having a thickness of 2 mm for example 2 and all comparative examples and 3 mm for example 1 only. The transformation is made by injection moulding.
The transmittance and reflectance is measured.
The colour shift in table 4 is calculated by subtracting the values obtained by reflectance from the ones obtained by transmittance. This values are representative of a visual observation when the light is off or on.
For the examples 1 and 2, but also for the comparative examples CEx1 and CEx2 a significant variation of the lightness value L* together with a very low variation of colour components a* and b* is observed. This corresponds to a change from dark to bright.
Also the injection moulded sheets that were prepared of 2 mm and 3 mm thickness of the compositions from examples 1 and 2 and comparative examples are compared to overmoulded injected samples. The same samples of 2 mm are also injection moulded and overmoulded with 1 mm a pure (meth)acrylic resin V825T from ALTUGLAS.
The gloss at 60° based on norm ASTM D523 is measured.
The comparative examples in table 5 show a muss lesser gloss. In order to obtain a high gloss the samples have to be overmoulded. With the composition according to the invention a high gloss is directly obtained after injection moulding
The composition according to the invention allows the preparation of high glossy surface for a compositing possessing for lightning applications an aspect contrast and/or color contrast independent of the color of lightning source, by one simple process step.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1859955 | Oct 2018 | FR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2019/079159 | 10/25/2019 | WO | 00 |
