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    • 专利摘要:
    In a prepolymer composition comprising at least one mono- or oligomer building block having at least one polymerisable CC double bond and at least one multifunctional monomer building block, the multifunctional monomer building block is a multifunctional monomer building block having at least two thiol groups selected from the group consisting of 3-mercaptopropionates, 3-mercaptoacetates, thioglycolates and Alkylthiols containing, that the mono- or Oligomerbaustein is selected with at least one polymerizable double bond from the group of acrylates, methyl acrylates, vinyl ethers, allyl ethers, propenyl ethers, alkenes, dienes, unsaturated esters, allyl triazines, allyl isocyanates and N-vinyl amides, and at least one surface-active release agent selected from the group of alkyl (meth) acrylates, poly-siloxane (meth) acrylates, perfluoroalkyl (meth) acrylates, perfluoropolyether (meth) acrylates, alkyl vinyl ethers, poly-siloxanes Vinyl ethers, perfluoroalkyl vinyl ethers and perfluoropolyether vinyls ther, as well as a photoinitiator are included, and use of the same.
    公开号:AT516559A1
    申请号:T888/2014
    申请日:2014-12-10
    公开日:2016-06-15
    发明作者:
    申请人:Joanneum Res Forschungsgmbh；
    IPC主号:
    专利说明:

    The present invention relates to a prepolymer composition comprising at least one mono- or oligomer building block having at least one polymerizable double bond and at least one multifunctional monomer building block as well as to a use thereof.
    Due to the rapid growth of nanotechnology in recent years, the production of nanostructured components in industrial manufacturing is becoming increasingly important, and such nanostructured components are usually produced from photopolymerizable prepolymer compositions. In particular, in security technology, the decoration sector, product marketing, surface finishing of various materials and other areas increasingly fine structures are used to achieve certain additional functions, such as self-cleaning surfaces or to cause decorative optical effects or anti-reflection and the like. For this purpose, nanotechnologically prepared structures, which are made of special Präpolymerzusammensetzungen used. An even more important application of such micro- and nanostructured films is in electronic, optical, sensory and magnetic devices, such as integrated circuits, displays, micro-optics and the like, since small feature sizes are the deciding factor for the functionality of these elements and therefore exist intensive efforts in the field of large-scale printed electronics to manufacture components on film substrates. Micro-and nano-structuring techniques, such as roll-to-roll, roll-to-plate or sheet-to-sheet imprint technologies, therefore play an important role in industrial film production and are always requiring new and improved formable films or compositions from which films produced in this way can be produced are.
    Industrial film refinement covers a very wide range, ranging from the improvement of mechanical or decorative surface properties to the integration of optical, sensory and electronic functionalities in the material film. In particular, roll-to-roll (R2R), roll-to-plate (R2P), and sheet-to-sheet (S2S) manufacturing processes allow high production speed and high throughput due to the continuous mode of production and large film sizes achievable, thereby reducing costs can be reduced and larger quantities of product can be made available. A crucial criterion and at the same time a limiting component for the use of such production techniques, however, is the fact that products often have structures with dimensions in the lower micrometer or nanometer range, on the one hand because of the high integration density of their individual components, but also to the functionality of the structures in the To ensure the order of magnitude of the wavelength used and to increase the total surface area. Conventional mass printing methods such as gravure printing, flexographic printing, screen printing, offset printing and the like, although allow an extremely high throughput of several 100 m per minute, but do not usually provide the necessary structural resolution range available. The only currently known technique that makes it possible to produce structures with minimal dimensions in the nanometer range in a parallel process is the so-called nanoimprint lithography (NIL), which is a highly precise embossing process and with which it is possible even the smallest structures on the corresponding substrate to mold.
    Roll-to-roll nanoimprint lithography processes have hitherto been industrially used above all for the production of embossed holograms, for example as counterfeit protection for banknotes. For this purpose, similar processes are used in the nanoimprint lithography process, but the embossed structures consist of diffraction gratings, resulting in a superficial relief. Roll-to-roll nanoimprint lithography processes have recently been used, above all, in continuous processes, whereby the necessary embossing pressure is ensured by film drawing and contact pressure of the counter roll. Decisive in such methods is that adhesion of the paint is avoided on embossing tool to subsequently achieve a defect-free demolding of the embossed article can. For a roll-to-roll nanoimprinting process, two different types of embossing tools are currently used, either the embossing profile can be produced directly on an embossing roll, or on a thin flexible sheet or foil material, which is subsequently secured about a roll. At present, as such, to be able to arrange a roll metal foils, so-called shims, made of nickel, wherein the production of such Nickelshims is relatively complicated. Therefore, attempts are being made to replace the nickel shims with embossed stamps of polymeric materials, with polymer materials having potentially lower surface energies than nickel, which reduces paint adhesion during the embossing process. Moreover, the manufacturing costs of polymer stamps are significantly lower, but they have the disadvantage that they are usually relatively easily deformable, so that they can be used only very limited as a stamp in the submicron range. Another disadvantage of embossing polymer materials crosslinking in free-radical chain reactions is that suitable materials can usually be completely crosslinked only in the absence of oxygen, which appears problematic in a roll process, since they do not cure sufficiently fast enough to be used in a roll-imprinting process. and thus their fidelity is relatively low, and they are also subject to a slow hardening process due to the usually high content by weight of urethane acrylate oligomers, so that a defect-free self-replication of the stamp in a roll process does not seem possible. For R2R embossing, however, complete reaction of the reactive C-C double bonds in the polymer stamp material prior to R2R embossing is especially necessary because they otherwise react with the CC double bonds in the embossing lacquer, which inevitably leads to sticking of the stamp and lacquer , w "* * V" * «· · ·
    The present invention now aims to provide a prepolymer composition with which it is possible to form both embossing lacquers which can be prepared therefrom and also polymer embossing tools for roll-to-roll nanoimprint lithography, with which it is possible to reliably and reliably not only structures in the subnanometer range to form the film surface formed from the prepolymer, but to print or replicate them in a variety of times and in particular to replicate and print on the embossing tool without separate application of a release material.
    To solve this problem, a prepolymer composition according to the invention is characterized essentially by the fact that the multifunctional monomer building a multifunctional monomer with at least two thiol groups selected from the group: 3-mercaptopropionates, 3-mercaptoacetates, thioglycolates and alkylthiols entält that the Monooder Oligomerbaustein with at least one polymerizable double bond from the group of acrylates, methyl acrylates, vinyl ethers, allyl ethers, propenyl ethers, alkenes, dienes, unsaturated esters, allyl triazines, allyl isocyanates and N-vinyl amides is chosen and that at least one surface-active non-stick additive selected from the group alkyl (Meth) acrylates, poly-siloxane (meth) acrylates, perfluoroalkyl (meth) acrylates, perfluoropolyether (meth) acrylates, alkyl vinyl ethers, poly-siloxane-vinyl ethers, perfluoroalkyl-vinyl ethers and perfluoropolyether-vinyl ethers and a photoinitiator are included.
    In accordance with the invention, the mono- or oligomer building block having at least one polymerizable double bond selected from the group of acrylates, methacrylates, vinyl ethers, allyl ethers, propenyl ethers, alkenes, dienes, unsaturated esters, allyl triazines, allyl isocyanates and N-vinyl amides is a rapid reaction with free-radical oxygen molecules in a initiated by the photoinitiator radical polymerization. The resulting in such a reaction peroxy radicals are very inert and do not react with carbon-carbon double bonds. For this reason, in the radical polymerization, each oxygen molecule leads to the termination of a polymerization chain reaction, which is undesirable. However, in the presence of a multifunctional monomer building block having at least two thiol groups, the peroxy radicals abstract hydrogen atoms from the thiol groups to form thionyl radicals, which in turn add to the carbon-carbon double bonds and start a polyaddition reaction. The thiol-induced polyaddition thus continues UV crosslinking. The simultaneous growth of many reaction centers leads to gelation only at very high conversions, e.g. in comparison to pure acrylate systems, whereby the growing molecules remain longer mobile, which leads to higher overall polymerization rates and higher conversion rates. At the same time, the generation of many reaction centers achieves more uniform cross-linking and lower tensions within the polymer, as well as greatly reduced shrinkage of the material upon solidification. In addition to the presence of a photoinitiator, it is advantageous to carry out the polymerization in addition to use at least one mono- or oligomer component having at least one polymerizable double bond which is selected from the group of acrylates, methacrylates, vinyl ethers, allyl ethers, propyl ethers, alkenes, dienes, unsaturated esters, Allyltriazine, allyl isocyanates and N-vinyl amides, as well as a surface-active release agent to add, thereby the adhesion energy, ie to reduce the adhesion between the embossing lacquer formed from the prepolymer composition and the shim or stamp, which enables a residue-free detachment of the two materials.
    By, as corresponds to a development of the invention, the prepolymer composition is developed so that the multifunctional monomer with at least two thiol groups in an amount of 1 wt .-% to 50 wt .-%, in particular from 5 wt .-% to 30 wt is contained .-%, and that two of the at least one polymerizable double bond-containing mono- or Oligomerbausteine in a total amount of 1 wt .-% to 90 wt .-%, in particular from 10 wt .-% to 50 wt .-% are included , On the one hand, by targeted use of the amount of at least two thiol multifunctional monomer unit which occurs during each polymerization shrinkage already effected in the liquid state, which in a subsequent UV embossing process, the Abformtreue compared to conventional materials is significantly improved. In particular, therefore, the prepolymer compositions according to the invention in the fully crosslinked state have a significantly reduced shrinkage compared to conventional polymers.
    By further containing two of at least one polymerizable double bond-containing mono- or oligomeric building blocks in a total amount of 1 wt .-% to 90 wt .-%, in particular from 10 wt .-% to 50 wt .-%, the polymerization rate can be selectively controlled become. The two mono- or oligomer building blocks having at least one polymerizable double bond differ in particular in their molecular weight. For example, one of the two mono- or oligomer building blocks having at least one polymerizable double bond can be a reactive monomer and the other an oligomer building block, as a result of which the material properties of a cured polymer produced therefrom can be adjusted in a targeted manner. Thus, an increase in the proportion of one of the two polymerizable double bond-containing mono- or oligomeric building blocks to a lowering of the rate of polymerization due to the reduced mobility or flexibility of the mono or Oligomerbausteine. An extension of side chains, in contrast, leads to a significant increase in the rate of polymerization and thus to increased conversions because of the higher mobility and flexibility of the mono- or oligomer building blocks. By selective choice of the amount of the two main constituents of the prepolymer composition used, it is thus possible, for example, to form a polymer composition, such as an embossing lacquer, which has extremely high conformability with simultaneously reduced shrinkage and high stability.
    By using urethane acrylate oligomers having a molecular weight of between about 300 g / mol and 2500 g / mol as the mono- or oligomer building block having at least one polymerizable double bond, a prepolymer composition can be obtained in a targeted manner to provide, which in a subsequent orders or applying the polymer layer in comparison to conventional layers achieve a uniform layer thickness, which is free of irregularities. This prepolymer composition has readily processable viscosities. In detail, e.g. Urethane acrylate oligomers or polyester oligomers of high viscosity and such viscosities make it difficult or prevent uniform application of a thin layer of the prepolymer composition by gravure or other coating methods such as inkjet and slit coating. To ensure that on the one hand, the viscosity is not too high and on the other hand, the layer thicknesses are not too large or irregular in particular, therefore, according to the invention proceeds so that the urethane acrylate Oligo mers with a higher molecular weight z. For example, acrylate monomers or vinyl ester monomers may be added as so-called reactive diluents in order to achieve uniform layer thicknesses and in particular not to raise the viscosity too much.
    According to one embodiment of the invention, it has proven to be advantageous to keep the viscosity of the prepolymer composition as low as possible and to allow a uniform applications of thin layers to proceed so that the mono- or Oligomerbausteine with at least one polymerizable double bond from the group the bifunctional urethane acrylate oligomers having a molecular weight between 300 g / mol and 1200 g / mol, trifunctional urethane acrylate oligomers having a molecular weight between 450 g / mol and 1750 g / mol and tetrafunctional urethane acrylate oligomers having a molecular weight between about 500 g / mol and 2500 g / mol are selected. Such a choice of the molecular weights as a function of the functionality of the urethane acrylate oligomer makes it possible, inter alia, to ensure the sufficiently rapid flow of the prepolymer into the stamp topography, whereby particularly extremely small structures can be molded safely and reliably.
    By, as corresponds to a development of the invention, the surface-active release agent contains an amount of 0.01 wt .-% to 10 wt .-%, in particular 0.1 wt .-% to 3 wt .-%, it is ensured that the surface energy of the prepolymer composition is reduced to such an extent that further generations of patterns can be repeatedly drawn without defects by embossing or molding. The surface energy of such embossing lacquers is in this case influenced to a significant extent by the surface energy of the adjacent phase, the lower the surface energy of the adjacent phase, the lower the surface energy of a polymer embossed from the prepolymer composition and the better the non-stick properties of the same. Such a low surface energy of the embossing master propagates in an embossing stamp thus formed and can also be maintained over several impressions.
    By, as corresponds to a development of the invention, the photoinitiator contained in the prepolymer composition from the group of thioxanthones, ketosulphone, (alkyl) - benzoyl-phenyl-phosphine oxides, 1-hydroxyalkylphenyl ketones or 2,2-dimethoxy-1,2-di-phenylethane -1-on, it is possible to initiate the polymerization effectively.
    By, as corresponds to a development of the invention, the photoinitiator in an amount of 0.1 wt .-% to 10 wt .-%, in particular 0.5 wt .-% to 5 wt .-%, the polymerization rate the composition can be controlled. In general, it should be noted that the higher the concentration of the photoinitiator, the greater the rate of polymerization in the thin films used, so that in particular an amount in the lower range of 0.5 wt .-% to 5 wt .-% of the photoinitiator has been found to be advantageous for a polymerization according to the invention.
    The higher the mass fraction of, for example, a urethane acrylate oligomer, the greater the hardness of the final polymeric composition, and therefore it is found that it is frequently required in the context of the present invention, in particular for adjusting, for example, the viscosity, the modulus of elasticity, Indentationshärte and the like. Add a reactive diluent, which, as is preferred according to the invention, the reactive diluent from the group of aliphatic (meth) acrylates or polyether (meth) acrylates, in particular HDDA, PEODA or TMP (EO ) xTA is selected. It has been found that the arm length of the thinner has a significant influence on the hardness of the polymer composition. With increasing proportion of reactive diluent and in particular the fact that as reactive diluent at least one multifunctional aliphatic or polyether (meth) acrylate, in particular ΤΜΡ (ΕΟ) 9ΪΑ, ΤΜΡ (ΕΟ) ΤΑΤΑ, ΤΜΡ (ΕΟ) 3ΪΑ or TMPTA is included In addition to the viscosity of the prepolymer composition, the hardness of the polymer composition can also be influenced in a targeted manner. Here, for example, the use of TMP (EO) 9TA leads to a strong reduction in the hardness of the polymer composition, whereas the use of TMP (EO) 3TA leads to a significantly lower reduction of the hardness of the polymer composition, so that by careful selection of the reactive diluent, the hardness the end product can be controlled specifically.
    The compound designated by the non-nomenclature name "trithiol" is trimethylolpropane tris- (3-mercaptoproprionate).
    By, as corresponds to a development of the invention, the prepolymer composition having a viscosity of 0.01 Pas to 1 Pas, a good flowability of the prepolymer composition is achieved, so that not only a uniform coating of surfaces to be molded surfaces is achieved, but also ensured in that the prepolymer composition flows sufficiently fast to fill also the depressions of very fine patterns sufficiently quickly and completely.
    In particular, in order to minimize or completely prevent adhesion of the prepolymer composition to surfaces such as, for example, a nickel shim surface, the invention is developed in such a way that additionally a silicone-containing or fluorine-containing additive selected from the group of monofunctional or polyfunctional polydimethylsiloxy is used. xan (meth) acrylates, perfluoro-n-alkyl (meth) acrylates or perfluoropolyether (meth) acrylates in an amount of 0.1 wt .-% to 3 wt .-% as a surface-active release agent is. Silicone-containing or fluorine-containing additives contribute to the reduction of the adhesion and to facilitate the detachment of the polymer compositions formed from the prepolymer composition of the embossing tool, in particular the perfluorinated additives have proven to be particularly favorable and reliably enable a plurality of impressions of a pattern.
    The invention further aims at the use of the prepolymer composition according to the invention for the formation of an embossing lacquer. Such embossing lacquers are particularly well-suited for use in roll-to-roll, roll-to-plate or sheet-to-sheet processes and exhibit excellent impression properties so that they can be used on an industrial scale. A particularly high number of cycles in an embossing process can be achieved according to the invention by the use of the prepolymer composition, which is characterized in that the cured prepolymer composition has a modulus of elasticity between 50 MPa and 5 GPa and a surface energy of 10 to 60 mJ / cm 2. Embossing lacquers which have a modulus of elasticity between 50 MPa and 5 GPa are sufficiently strong and sufficiently flexible and show sufficiently low adhesion energies to be replicated repeatedly, without fear of impairment, in particular distortion, of the sample. Due to the possible extremely low surface energy and thus adhesion energy, it is still possible to carry out several generations of imprints and impressions without damaging it by adhering embossing lacquer.
    Finally, the invention is directed to a use of the prepolymer composition for continuous patterning and in situ UV curing in a roll-to-roll imprinting process, as well as for the production of self-moldable stamping dies for UV embossing of substantially similar polymers. Although comparative prepolymer compositions may have been used in other technical fields as well, it has surprisingly been found that embossing lacquers for a roll-to-roll imprinting process can be formed in situ from a prepolymer composition, with which a plurality of impressions without damage to the printing pattern and in particular faithful impressions of nanostructured topographies can be achieved.
    Furthermore, as is the case with a development of the invention, it is possible to use the prepolymer composition as a self-impressionable embossing punch for embossing substantially similar embossing lacquers.
    The invention will be explained in more detail with reference to embodiments and drawings. In this show
    1 shows a diagram which shows the influence of the amount of the multifunctional monomer building block with at least two thiol groups on the conversion of the C-C double bonds as a function of time when the prepolymer composition is cured by UV irradiation,
    2 shows an analogous diagram as in FIG. 1, which shows the influence of the amount of mono- or oligomer component on the conversion of the C-C double bonds as a function of time when the prepolymer composition is cured by UV irradiation,
    3 shows a diagram which shows the influence of the individual components of the prepolymer on the dynamic viscosity of the prepolymer,
    4 shows a diagram which shows the profile of the modulus of elasticity as a function of the concentration of the individual constituents of the prepolymer,
    FIG. 5 shows the change in the surface energy of the prepolymer composition as a function of the amount of nonstick additive used, and FIG
    6, 7 and 8 show examples of the self-replicability of embossing lacquers made on the basis of the prepolymer composition according to the invention, wherein Fig. 6 shows a urethane acrylate polymer die molded from a nickel master (Fig. 6a) and a polymer embossment (Fig. 6b), FIG. 7 shows an analogous representation, in which FIG. 7a shows a urethane acrylate master, FIG. 7b shows the urethane acrylate embossing stamp molded therefrom on film, and FIG. 7c shows the embossing in a urethane produced with the film 8 shows an example of the transfer of three-dimensional structures with a urethane acrylate embossing die according to the invention, FIG. 8a showing the silicon embossing master, and FIG. 8b showing the urethane acrylate polymer. Roller stamp in roll-to-roll UV imprint method produced embossing on foil shows.
    Example 1 shows the influence of the addition of a multifunctional monomer with at least two thiol groups on the polymerization kinetics.
    Specifically, varying amounts of trithiol (trimethylolpropane tris (3mercapto-propionate)), each containing a prepolymer matrix containing 4.5% tetrafunctional urethane acrylate oligomer (UAO), 0.5% release agent, polydimethylsiloxane, 3% and 5% of a photoinitiator, respectively 2-hydroxy-2-methyl-1-phenyl-propan-1-one and a reactive diluent TMP (EO) 3TA added. As the proportion of trithiol increases, the content of reactive diluent TMP (EO) 3TA is reduced to the same extent. As is clear from Fig. 1, the reaction kinetics are significantly accelerated, the higher the content of trithiol. From Fig. 1 is further recognizable that the higher the content of trithiol, the higher the content of reacted double bonds. From Fig. 1 it is finally apparent that at a 30% trithiol already after a few seconds complete conversion of all C-C double bonds has taken place, and that an increase of the photoinitiator of 3% to 5% also leads to an acceleration of the polymerization.
    It follows from this that the higher the proportions of trithiol or moieties of multifunctional monomer building blocks which have at least two thiol groups in the prepolymer composition, the faster is the complete conversion of the CC double bond, such prepolymer compositions being used, for example, as embossing lacquers (Imprintlacke ) are usable. An incomplete conversion of the C-C double bonds in the short available exposure time of <1 s, with e.g. 2 W / m2 in an R2R embossing process would lead to an adhesive surface, whereby a separation of the paint from the stamp does not appear possible and it may, for example, to Lackanhaftungen on the stamp come. The addition of multifunctional monomer building blocks with at least two thiol groups allows such rapid reaction of the C-C double bonds that the embossing lacquers can be used in a continuous roll-to-roll UV nanoimprint lithography process. An increase of the urethane oligomer acrylate content in a prepolymer matrix of 9.5% trithiol, 0.5% polydimethylsiloxane as nonstick additive, 3% 2-hydroxy-2-methyl-1-phenyl-propan-1-one as photoinitiator and TMP (EO) 3TA as a residual reactive diluent leads to a deceleration of the polymerization kinetics, as can be seen in FIG. The higher the content of the urethane acrylate oligomer (i.e., the mono or oligomer building block having at least one polymerizable double bond), the slower the polymerization kinetics become, which is explained by an increase in viscosity and thus a reduction in the mobility of the radicals. The consequence of this is a faster attainment of the gel point, a lower conversion rate and ultimately a lower degree of conversion. It can be seen from FIGS. 1 and 2 that for use as imprint coatings, a prepolymer composition must have the highest possible content of multifunctional monomer building blocks with at least two thiol groups. By way of example, the following prepolymer composition is mentioned: 20% trithiol, 35% <x <60% UAO, (74.5-x)% TMP (EO) 3TA, 5% photoinitiator and 0.5% non-stick additive, which prepolymer composition is replaced by a characterized complete conversion and thus produced coatings are characterized by a particularly high scratch resistance.
    Example 2
    A prepolymer mixture consisting of urethane acrylate oligomer, reactive diluent, photoinitiator, multifunctional monomer building block having at least two thiol groups, especially trithiol and photoinitiator was examined for viscosity change by measuring the influence of chain length of the oligomer building block with at least one polymerizable double bond on viscosity , the concentration of the monomer with at least two thiol groups on the viscosity, and the reactive diluent on the viscosity examined. As can be seen from FIG. 3, the dynamic viscosity increases with at least two polymerizable double bonds as a function of the chain length of the oligomer component. It can be seen from this experiment that the higher the proportion of the oligomer component, the higher the viscosity of the prepolymer system. Since it is favorable for a roll-to-roll process if the prepolymer composition has a dynamic viscosity below 1.0 Pas, and it has been found in further experiments that using such prepolymer compositions smooth, uniformly thick layers can be achieved , Of course, the lower the viscosity of the embossing lacquer, the sooner complicated structures of the embossing relief in the stamper can be filled out sufficiently fast during a roll-to-roll embossing process and can be transferred exactly as a result.
    It can be seen from Figure 3 that an optimum prepolymer composition for an imprint varnish has a proportion of less than 60% urethane acrylate oligomer with a molecular weight <1000 g / mol, and that the concentrations of the other components, such as nonstick additive , multifunctional monomer building blocks with at least two thiol groups, photoinitiator and, as well as the nature of the reactive diluent, have only a slight influence on the viscosity.
    Example 3 shows how the mechanical strength, i. the reduced Young's modulus E * of the tetrafunctional UAO at 600 g / mol after exposure, i. Networking with by 1 min. Pre-cure at 5 mW / cm2 with the Waldmann UV source and final cure for 1 min. at 2.2 W / cm2 depending on the composition changed.
    As can be seen in Figure 4, there is an increase in modulus of elasticity as the proportion of oligomer building block increases with at least one polymerizable double bond, e.g. a tetrafunctional urethane acrylate oligomer with different molecular weights between 600 g / mol and 1000 g / mol, in a prepolymer matrix of (96.5-x)% TMP (EO) 3TA, where x is the amount of oligomer building blocks having at least one polymerizable double bond or ΤΜΡ (ΕΟ) 9ΪΑ or tri-thiol, and 3% 2-hydroxy-2-methyl-1-phenyl-propan-1-one as a photoinitiator and 0.5% polydimethylsiloxane acrylate as an anti-adhesion additive. The maximum E * values are at 5 GPa at a concentration of 80% urethane acrylate oligomer, the increase in the modulus of elasticity resulting from the fact that the oligomers have a higher number of crosslinkable acrylate groups.
    Likewise, it can be seen that the modulus of elasticity of the cured polymer decreases as the side arm length - i. the number of ethoxy groups - the monomer used as reactive Ver thinner with at least one polymerizable double bond selected from TMPTA, TMP (EO) 3TA, TMP (EOe) TA, TMP (EC> 9) TA increases, as shown in the table below is. It can also be seen from this table that the higher the molecular weight - i. the side arm length - or number of ethoxy groups - of the reactive diluent, the greater the degree of conversion of the double bonds, wherein the diluent was introduced in each case in an amount of 65% of Gesamtpräpolymerzusammensetzung. The curing of the polymer was carried out for 1 min at 5 mW / cm 2.
    Table 1
    As a result of the experiment of Example 3, there is a decrease in the modulus of elasticity upon addition of trithiol, which is substantially related to the lowering of the glass transition temperature in thiolene polymerization - addition of trithiol.
    The ideal composition of a prepolymer for an embossing die with high hardness and 100% conversion by post-curing thus results in: 5% trithiol, 35 × 60% UOA, (89.5 ×)% TMP (EO) 3 × TA, 5% photoinitiator and 0.5% non-stick additive. Fast cross-linking is not so necessary for the production of the embossing stamp, as it can be stamped much slower and, in addition, post-hardening is possible.
    A second ideal composition for the almost complete conversion imprint varnish would be: 5% trithiol, 35 <x <60% UAO, (89.5-χ)% ΤΜΡ (ΕΟ) ΤΑΤΑ, 5% photoinitiator, and 0.5% release-adhesion additive no postcuring is necessary.
    Example 4 shows the influence of the amount of a release agent on the surface energy of the prepolymer.
    As can be seen from Fig. 5, by adding a perfluoropolyether acrylate (HFPO-A) as an anti-adhesion additive at concentrations lower than 1%, the surface energy of the prepolymer can be extremely reduced when it is cured against air / argon. On the other hand, it can be seen that when the prepolymer is cured against an untreated nickel surface, the high surface energy of the nickel is "copied" into the paint and no substantial lowering of the surface energy of the embossed polymer is achieved despite the addition of an anti-adhesion additive. On the other hand, when curing occurs during embossing over a nickel surface treated with a self-assembled, fluorinated alkyl monolayer, the low surface energy of this monolayer is copied and, in turn, the surface energy of the embossed, cured polymer is lowered, as can also be seen in FIG ,
    It can thus be seen that the addition of nonstick additives to a prepolymer composition, of any composition in a concentration between 0.1% and 0.5%, results in a significant reduction in the surface energy when cured against a low-energy surface, so that a defect-free demolding of the cured Polymer is possible.
    Example 5
    Self-replications of prepolymer compositions based on a mono-or oligomer building block with at least one polymerizable double bond and at least one multifunctional monomer building block with at least two thiol groups.
    The prepolymer compositions exhibit excellent self-replicability, especially in a roll-to-roll nanoimprint lithography process. In order for such self-replicability to be present, the polymer stamping lacquer must be completely cured, that is to say: completely REPLACED. In Fig. 6, a urethane acrylate oligomer based polymer stamp has been molded from a nickel master (Fig. 6a) and then an R2R impression has been made therefrom. (Fig. 6b), from which it can be seen that Fig. 6b is a mirror image to Fig. 6a.
    FIG. 7 shows the replication of non-regular and undercut 3D structures, the illustrated figures being diatom structures. 7a shows the urethane acrylate master, FIG. 7b shows a molded urethane acrylate oligomer embossing stamp on film, and FIG. 7c shows an embossment produced in a urethane acrylate oligomer embossing lacquer according to FIG. 7b by means of a roll-to-roll process Invention.
    It is shown in Figure 8 that also the transfer of 3D structures having undercuts with a high aspect ratio, such as, for example, silicon etched columnar structures, into the urethane acrylate oligomer embossing lacquer is possible in a roll-to-roll process. In Fig. 8a in this case the positive Si master is shown. A negative urethane acrylate oligomer embossing stamp was prepared from this Si master, and FIG. 8b shows the embossment produced with this embossing stamp in a roll-to-roll UV nanoimprint lithography process (R2R-UV-NIL).
    FIGS. 6 to 8 are electron micrographs of line structures with 400 nm spacing and 600 nm width, which were transferred into the urethane acrylate oligomer embossing lacquer in an R2R process at a web speed of 10 m / min.
    Example 6
    Production of water and dirt repellent polymer films
    The preparation of water-repellent and soil-repellent or self-cleaning polymer films having prepolymer compositions containing 10% by weight to 90% by weight of a mono- or oligomer building block having at least one polymerizable double bond, in particular low-viscosity, multifunctional, aliphatic polyurethane acrylates, 10% by weight to 90% Wt .-% of a multifunctional, reactive diluent selected from the above group, 1 wt .-% to 10 wt .-% of a photoinitiator, in particular 2-hydroxy 2-methyl-1-phenyl-propan-1-one and 0.1 % By weight to 3% by weight of a surface-active release polymer, in particular 1H, 1H, 2H, 2H-tridecafluorooctyl acrylate, makes it possible to produce embossing lacquers from the prepolymer composition which have an extremely low surface energy of 12 mJ / m 2. Being highly efficiently adsorbed on the paint surface, the surface release agent forms a dense monolayer of high CF3 content which makes it possible to make films which, when simultaneously using an embossing tool with correspondingly reduced surface energy, such as nickel stamping surfaces or silicon or quartz surfaces Stamp, each with long-chain active perfluoroalkyl phosphonic acids, such as 1H, 1H, 2H, 2H tridecafluoroctyl phosphonic acid are assigned to provide a stamp material having an equally low surface energy of 12 mJ / m2. In order to further reduce the water / polymer contact surface, which must be as small as possible for a water-repellent or dirt-repellent effect, the paint surface is subsequently microstructured or nanostructured, as a result of which the contact angle with water can be increased to more than 170 ° with one simultaneously very low contact angle hysteresis and the rolling angle of water droplets can be lowered to <2 °. Merely for comparison it is stated that smooth surfaces of the embossing lacquer have a contact angle of about 115 ° with water, so that the water-repellent effect can be achieved only with strong inclination of the film itself, whereas in a structured film water does not even on a nearly flat surface can stick.
    权利要求:
    Claims (16)
    [1]
    claims:
    1. prepolymer composition comprising at least one mono- or oligomer building block having at least one polymerisable CC double bond and at least one multifunctional monomer building, characterized in that the multifunctional monomer building a multifunctional monomer building with at least two thiol groups selected from the group: 3-mercaptopropionates, 3rd -Mercaptoacetate thioglycolates and alkylthiols, that the mono- or oligomer unit having at least one polymerizable double bond from the group of acrylates, methyl acrylates, vinyl ethers, allyl ethers, propenyl ethers, alkenes, dienes, unsaturated esters, allyl triazines, allyl isocyanates and N -Vinylamide is selected and that at least one surface-active non-stick additive selected from the group alkyl (meth) acrylates, poly-siloxane (meth) acrylates, perfluoroalkyl (meth) acrylates, perfluoropolyether (meth) acrylates, alkyl vinyl ethers , Poly-siloxane-vinyl ethers, perfluoroalkyl-vinyl ethers and Per fluoropolyether vinyl ethers, and a photoinitiator are included.
    [2]
    2. prepolymer composition according to claim 1, characterized in that the multifunctional monomer with at least two thiol groups in an amount of 1 to 50 wt .-%, in particular from 5 wt .-% to 30 wt .-% is contained and that two of the at least one polymerizable double bond-containing mono- or Oligomerbausteine in a total amount of 1 wt .-% to 90 wt .-%, in particular from 10 wt .-% to 50 wt .-% are included.
    [3]
    3. prepolymer composition according to claim 1 or 2, characterized in that are used as mono- or oligomer unit having at least one polymerizable double bond urethane acrylate oligomers having a molecular weight between about 300 g / mol and 2500 g / mol.
    [4]
    4. prepolymer composition according to claim 3, characterized in that the mono- or Oligomerbausteine with at least one polymerizable double bond from the group bifunctional urethane acrylate oligomers having a molecular weight between 300 g / mol and 1200 g / mol, trifunctional urethane acrylate oligomers having a molecular weight between 450 g / mol and 1750 g / mol and tetrafunctional urethane acrylate oligomers having a molecular weight of between about 500 g / mol and 2500 g / mol.
    [5]
    5. prepolymer composition according to claim 1, 2 or 3, characterized in that the surface-active release agent in an amount of 0.01 wt .-% to 10 wt .-%, in particular 0.1 wt .-% to 3 wt .-% is.
    [6]
    6. prepolymer composition according to one of claims 1 to 5, characterized in that the photoinitiator from the group of thioxanthones, Ketosulphone, (alkyl) benzoyl-phenyl-phosphine oxides, 1-hydroxyalkyl phenyl ketones or 2,2-dimethoxy-1,2 -diphenyl-ethane-1-one is selected.
    [7]
    7. prepolymer composition according to claim 6, characterized in that the photoinitiator in an amount of 0.1 wt .-% to 10 wt .-%, in particular 0.5 wt .-% to 5 wt .-% is included.
    [8]
    8. prepolymer composition according to one of claims 1 to 7, characterized in that at least one monomer unit is contained with at least one polymerizable double bond as a reactive diluent.
    [9]
    9. prepolymer composition according to claim 8, characterized in that the reactive diluent from the group of aliphatic (meth) acrylates or polyether (meth) acrylates, in particular HDDA or TMP (EO) xTA is selected.
    [10]
    10. prepolymer composition according to claim 9, characterized in that as reactive diluent at least one multifunctional aliphatic or polyether (meth) acry-lat, in particular TMP (EO) 9TA, TMP (EO) 6TA, TMP (EO) 3TA orTMPTA is included.
    [11]
    11. prepolymer composition according to one of claims 1 to 9, characterized in that it has a viscosity of 0.01 Pas to 1 Pas-.
    [12]
    12. prepolymer composition according to one of claims 1 to 11, characterized in that the surface-active non-stick additive is a silicone-containing or fluorine-containing additive selected from the group of mono- or polyfunctional polydimethylsiloxane (meth) acrylates, perfluoro-n-alkyl (meth -) - acrylate or perfluoropolyether (meth) - acrylates in an amount of 0.1 wt .-% to 3 wt .-% is contained.
    [13]
    13. Use of the prepolymer composition according to one of claims 1 to 12 as embossing lacquer, wherein the cured prepolymer composition has an modulus of elasticity between 50 MPa and 5 GPa.
    [14]
    14. Use of the prepolymer composition according to claim 13, characterized in that the embossing lacquer has a surface energy of 10 mJ / m 2 to 60 mJ / m 2.
    [15]
    15. Use of the prepolymer composition for the production of self-formable embossing stamps for UV embossing of substantially similar polymers.
    [16]
    16. Use according to claim 13, characterized in that it is used for continuous structuring and in situ UV curing in a roll-to-roll imprinting process. Vienna, Joanneum Research ForschereJ ^ gesellschaft mbH by: f CUNOWT ^ atehianwcttts KG
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    同族专利:
    公开号 | 公开日
    JP6640870B2|2020-02-05|
    CN107533287A|2018-01-02|
    HK1244068B|2020-03-20|
    US20170349707A1|2017-12-07|
    JP2018505288A|2018-02-22|
    US10308768B2|2019-06-04|
    CN107533287B|2021-06-01|
    WO2016090395A1|2016-06-16|
    AT516559B1|2017-12-15|
    EP3230796A1|2017-10-18|
    ES2743812T3|2020-02-20|
    KR20170093229A|2017-08-14|
    EP3230796B1|2019-06-05|
    DK3230796T3|2019-07-15|
    WO2016090395A8|2018-09-07|
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    法律状态:
    2018-03-15| HA| Change or addition of new inventor|Inventor name: MARKUS LEITGEB, AT Effective date: 20180119 Inventor name: STEPHAN RUTTLOFF, AT Effective date: 20180119 Inventor name: DIETER NEES, AT Effective date: 20180119 Inventor name: VALENTIN SATZINGER, AT Effective date: 20180119 Inventor name: BARBARA STADLOBER, AT Effective date: 20180119 Inventor name: ANDRE LINTSCHNIG, AT Effective date: 20180119 |
    优先权:
    申请号 | 申请日 | 专利标题
    ATA888/2014A|AT516559B1|2014-12-10|2014-12-10|A prepolymer composition comprising such composition and use thereof|ATA888/2014A| AT516559B1|2014-12-10|2014-12-10|A prepolymer composition comprising such composition and use thereof|
    CN201580075848.3A| CN107533287B|2014-12-10|2015-12-09|Polymer or prepolymer composition or embossing lacquer comprising such a composition and use thereof|
    DK15817054.8T| DK3230796T3|2014-12-10|2015-12-09|POLYMER OR PRE-EMBODIMENT COMPOSITION OR PREVENTION WITH A COMPOSITION AND USE THEREOF|
    KR1020177018946A| KR20170093229A|2014-12-10|2015-12-09|Poly- or prepolymer composition, or embossing lacquer comprising such a composition and use thereof|
    PCT/AT2015/000157| WO2016090395A1|2014-12-10|2015-12-09|Poly- or prepolymer composition, or embossing lacquer comprising such a composition and use thereof|
    ES15817054T| ES2743812T3|2014-12-10|2015-12-09|Composition of prepolymer or printing lacquer, comprising such a composition and use thereof|
    EP15817054.8A| EP3230796B1|2014-12-10|2015-12-09|Poly- or prepolymer composition, or embossing lacquer comprising such a composition and use thereof|
    US15/534,392| US10308768B2|2014-12-10|2015-12-09|Poly- or prepolymer composition, or embossing lacquer comprising such a composition and use thereof|
    JP2017549555A| JP6640870B2|2014-12-10|2015-12-09|Polymer or prepolymer compositions or embossed paints containing such compositions and uses of embossed paints|
    HK18103675.6A| HK1244068B|2014-12-10|2018-03-16|Poly- or prepolymer composition, or embossing lacquer comprising such a composition and use thereof|
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