Dual Cure Isocyanate Inkjet Composition

Abstract

An inkjet composition is provided. [Solution] An inkjet composition having 1.8 to 3.3 mol / kg of acryloyl groups, the inkjet composition comprising: (i) a photopolymerization reactive compound (M) containing exactly one acryloyl group; (ii) a photopolymerization reactive compound (N) containing at least two acryloyl groups; (iii) a radical photoinitiator (R); (iv) an isocyanate compound (D) containing at least two isocyanate groups; and (v) a compound (H) containing at least one hydroxyl group, wherein (M) is different from (D); (N) is different from (D); and (H) is different from (D), (M), and (N); 10 to 28 mol % of the acryloyl groups contained are provided by the reactive compound (N), and a molar ratio of the acryloyl groups contained in the inkjet composition to the isocyanate groups contained in the compound (D) is 0.9 to 3.3.

Description

[Technical field]

[0001] explanation The present invention relates to an ink jet composition, its use, a method for printing three-dimensional objects, and to a three-dimensional object. [Background technology]

[0002] Three-dimensional (3D) printing, or additive manufacturing, is a process in which 3D digital models are produced by additive growth of a building material. 3D printed objects are produced by utilizing computer-aided design (CAD) data of an object for the successive construction of two-dimensional (2D) layers that correspond to cross sections of the 3D object. These layers are printed on top of each other, with the condition that each layer is rapidly cured (e.g. by UV curing) before the next layer is printed accordingly.

[0003] One method of performing said 3D printing is inkjet printing: in inkjet printing, small droplets of ink (with a defined viscosity) are projected directly onto the receiving surface without physical contact between the printing device and the ink receiving side. The printing device electronically stores the printing data and controls a mechanism for imagewise ejection of the droplets. Printing is achieved by moving the print head across the ink receiving side or vice versa, or both.

[0004] Three-dimensional inkjet printing is a relatively fast and flexible printing method for the production of prototype parts, and it creates and rapidly manufactures three-dimensional complex structures directly from CAD files. Radiation-curable compositions used in three-dimensional printing methods of complex structures are described, for example, in WO2004 / 096514. However, in general, there are many radiation-curable compositions described in the art that can be used in the field of inkjet printing, such as in WO2020 / 109769, US2015 / 064417, US10005911, and US2009 / 105363. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0005] The challenges faced by the 3D printing are poor mechanical properties, such as low heat distortion temperature, brittleness, and aging, where aging means embrittlement over time and / or under temperature changes and / or humidity. Another challenge faced by the 3D printing is incomplete curing of the (initial) printed 3D object (the so-called "green body"), as well as some quality issues with the final product (e.g. mechanical aspects and / or product aging). If the 3D object is completely cured during the 3D printing process, the interlayer adhesion may be too weak and the print may fail.

[0006] However, uncured resin inside the final product is also undesirable: First, leakage of uncured liquid resin ("bleed") from the printed 3D object can cause health problems for the end user because the liquid resin may contain reactive chemicals. Second, the printed 3D object does not reach optimal mechanical performance because the uncured liquid resin may soften the object. Third, the uncured resin may cause problems in some industrial applications of the object, where high chemical inertness is required. A corresponding post-curing of the 3D "green body" is necessary to fully cure the printed "green body" object (to avoid the aforementioned drawbacks).

[0007] Therefore, a suitable inkjet printing ink must simultaneously combine (satisfy) the following conditions: have a sufficiently low viscosity (to allow printing of small droplets through the inkjet nozzle), provide high viscosity stability (e.g. should not polymerize in the printing device prior to printing), be sufficiently pre-curable (each printed ink layer needs to be pre-cured before the next layer is printed), and be efficiently post-curable (fully curable in a later step to provide the quality characteristics required for the 3D object).

[0008] Therefore, an object of the present invention is to provide an inkjet composition having 1.8 to 3.3 mol / kg of acryloyl groups, (i) a photopolymerizable reactive compound (M) containing exactly one acryloyl group; (ii) a photopolymerization reactive compound (N) containing at least two acryloyl groups; (iii) a radical photoinitiator (R); (iv) an isocyanate compound (D) containing at least two isocyanate groups, and (v) Compounds (H) containing at least one hydroxyl group Including, (M) is different from (D), except that an isocyanate compound containing exactly one acryloyl group and further containing at least two isocyanate groups is to be included in (D); (N) is different from (D), except that an isocyanate compound containing at least two acryloyl groups and further containing at least two isocyanate groups is to be included in (D); (H) is different from (D), (M), and (N); The object of the present invention is to provide an inkjet composition, in which 10 to 28 mol % of the acryloyl groups contained therein are provided by the reactive compound (N), and the molar ratio of the acryloyl groups contained therein to the isocyanate groups contained in the compound (D) is 0.9 to 3.3.

[0009] The isocyanate compound (D) containing at least two isocyanate groups may, and this is preferred, contain these isocyanate groups in blocked form.

[0010] The acryloyl group according to the present invention is defined as H2C=CH-C(=O)- (which may be part of an "acrylic ester group" of the type H2C=CH-C(=O)-O-). These groups are highly reactive and efficient free radical polymerization groups (much more reactive than, for example, methacrylic groups).

[0011] A photopolymerization reactive compound (M) "containing exactly one acryloyl group" means that it contains no more than one and no less than one acryloyl group.

[0012] By (M) is different from (D), it is meant that photopolymerization reactive compounds (related species) that contain exactly one acryloyl group and further contain at least two cyanate groups should be included in (D) (rather than (M)). However, the use of such "hybrid" components is not preferred (and may be avoided).

[0013] Accordingly, (N) is different from (D) means that the photopolymerization reactive compound (related species) containing at least two acryloyl groups and further containing at least two cyanate groups should be included in (D) (rather than (N)). However, the use of such "hybrid" components is not preferred (and may be avoided).

[0014] By (H) being different from (D), (M), and (N), it is meant that the relevant "hybrid" moieties (which contain at least one hydroxyl group and the relevant specific group of (D), (M), or (N)) should be included in (M), (N), or (D) but not in (H). In other words: (H) is different from (D), (M), and (N), but a compound that (on the one hand) contains at least one hydroxyl group and (on the other hand) meets the conditions to be (D), (M), or (N) should not be included in (H).

[0015] According to the present invention, the inkjet composition comprises (M) and (N) photocurable compounds (based on "photoinitiation"), and further (D) a thermally curable compound.

[0016] Photocurable compounds can be polymerized and / or crosslinked in an initial step by free radical (photo)polymerization, while thermocurable compounds react (via polyaddition) in a later thermal post-cure step.

[0017] The inkjet composition according to the present invention meets the relevant quality requirements: The composition provides the basis for a sufficiently low viscosity to allow the production of small (ink-jettable) ink droplets. In addition, the composition provides the basis for sufficient viscosity stability, which is a fundamental requirement to keep the printing process running (e.g., gelling of the ink would clog or even destroy the printer).

[0018] Furthermore, the inkjet composition according to the invention allows the production of pre-products with sufficient mechanical properties, in particular with sufficient "green body strength": the green body strength describes the stability of the object after photocuring and before thermal curing. The green body strength is a measure of the stability and crosslinking of the photocured object. However, it is not desirable to provide too high a green body strength: during post-processing (thermal curing), the UV system ensures the consistency of the shape, meaning that the thermal system is kept in place before and during its curing / fixing. However, once the thermal system starts to cure, depending on its properties (especially if the crosslinking in the first photopolymerization step is too strong), internal strains may occur, which may destroy (crack) the UV-cured structure. The inherent technically typical roughness of the relevant surfaces leads to easier crack formation due to the generation of internal strains. The use of the inkjet composition according to the invention offers a kind of "compromise" that takes into account all of these different issues involved - in particular: on the one hand the crosslinks need to be sufficiently rigid to provide strength for the green body and to keep the thermoset system in place, but on the other hand they must not be too brittle in order to withstand the thermoset.

[0019] The special "crosslinking strategy" justifying the advantages according to the present invention is reflected in the "rules" underlying inkjet compositions, which are crucially justified by the conformity with the following (key) parameters (I), (II) and (III): (I) an inkjet composition having 1.8 to 3.3 mol / kg of an acryloyl group; (II) 10 to 28 mol % of the acryloyl groups contained therein are provided by the reactive compound (N); The molar ratio of the acryloyl group contained in (III) to the isocyanate group contained in the compound (D) is 0.9 to 3.3.

[0020] (Key) Parameter(I): If the value is too high, relatively strong tensions will be created in the green body - promoting subsequent crack formation - and if the value is too low, the strength of the green body will deteriorate: what ultimately comes down to is a suitable compromise between providing strength and elasticity, among others.

[0021] (Key)Parameter(II): This parameter also offers a practical compromise between strength (of the green body) and elasticity: polyacrylates in particular are crucial for the formation of a network and thus for sufficient green body strength.

[0022] The monoacrylates especially contribute to the toughness-compatibility balance of the matrix network of the IPN with respect to tension compensation during thermal post-cure, and control of the hard and soft phases and phase domains.

[0023] The right balance between the strength of the green body and the efficiency of the post-cure is ensured by following parameter (II): too low a value will cause insufficient green strength, whereby too high a value will usually prevent thermal post-cure: (excessively) high network density of acrylate systems reduces the mobility (reduced reactivity of the thermal post-cure system), which can typically promote cracking.

[0024] Furthermore, matching with parameter II prevents undesired phase separation (due to segregation) during printing applications.

[0025] (Key)Parameter(III): In the broadest sense, this parameter ensures a balanced ratio of pre-curing and post-curing stabilization, and particularly concerns a compromise between the strength of the green body and the strength of the final body.

[0026] As the degree of hardening of the first network (pre-hardening) increases, stronger stresses arise in the green body during the formation of the second thermal network (post-hardening) (which promotes the formation of cracks (disadvantageously associated with too high values)), but also ensures the suitability of the interpenetrating network formation. However, sufficient green body strength is essential (too low values ​​are ultimately disadvantageous in this respect).

[0027] Parameter (III) is always understood in combination with parameter (I) as a relative ratio, which ultimately determines the network density of both networks.

[0028] A further advantage offered with respect to the use of the inkjet composition according to the invention is the avoidance of "bleeding" of the printed object before and during thermal curing (especially during removal of the support structure by the aqueous liquid and during thermal curing): leakage of liquid raw materials from the printed 3D object can cause health problems for the end user, since the liquid resin may contain reactive chemicals.

[0029] According to a particular embodiment of the present invention, the inkjet composition can be provided as a kit: the corresponding kit-in-part inkjet composition can comprise a combination of at least one photocurable compound and at least one thermally curable compound, and a separate photoinitiator. The kit-in-part inkjet composition can comprise a combination of at least one photocurable compound, at least one thermally curable compound, and a photoinitiator, and a separate curing catalyst. However, in most cases it is neither necessary nor advantageous to provide such a kit (the kit can be avoided).

[0030] According to a preferred embodiment, the inkjet composition according to the present invention has 2.0-3.0 mol / kg of acryloyl groups. Typically, in the inkjet composition, 10-25 mol% of the contained acryloyl groups are provided by the reactive compound (N). The appropriate (quantitative) combination of the two features "mol / kg of contained acryloyl groups" and "mol% of contained acryloyl groups provided by the reactive compound (N)" is also important with respect to providing a pre-product (and also a final product) which, on the one hand, is not too brittle (prone to cracks) and, on the other hand, is not too soft.

[0031] According to a preferred embodiment, in the inkjet composition, 90-100 mol %, preferably 95-100 mol %, of the reactive compound (N) is provided by species containing 3 or less acryloyl groups. However, it is important to note this regularity in combination with the other features "mol / kg of contained acryloyl groups" and "mol % of contained acryloyl groups provided by reactive compound (N)". Because it has been confirmed that the (appropriate quantitative) combination of these features is a fundamental requirement for providing a processing process on the one hand and for producing a high quality product on the other hand.

[0032] Monoacrylates (particularly compound (M)) often contribute to the medium viscosity of the inkjet composition (particularly species with medium molecular weight). The higher the amount of monoacrylate, the lower the degree of crosslinking.

[0033] The following monoacrylates can be used: Ethyl acrylate, stearyl acrylate, tetrahydrofurfuryl acrylate, lauryl acrylate, 2-phenoxyethyl acrylate, isodecyl acrylate, isooctyl acrylate, tridecyl acrylate, caprolactone acrylate, ethoxylated nonylphenol acrylate, isobornyl acrylate, hexadecyl acrylate, monomethoxytripropylene glycol monoacrylate, monomethoxyneopentyl glycol propoxylate monoacrylate, B-carboxyethyl acrylate, and / or oxyethylated phenol acrylate.

[0034] According to a preferred embodiment, the monoacrylate may be selected from dihydrodipentadienyl acrylate (CAS: 12542-30-2), cyclic trimethylolpropane formal acrylate (CAS: 66492-51-1), tricyclodecane methanol acrylate (CAS: 93962-84-6), 2-phenylethyl acrylate (CAS: 3530-36-7), 2-hydroxy-3-phenoxypropyl acrylate (CAS: 16969-10-1), 2-[(butylcarbamoyl)oxy]ethyl acrylate (63225-53-6), and / or 4-hydroxybutyl acrylate (2478-10-6).

[0035] However, the most preferred monoacrylate species are isobornyl acrylate, acryloylmorpholine, 2-[(butylcarbamoyl)oxy]ethyl acrylate, or mixtures thereof.

[0036] The following diacrylates can be used: 1,3 butylene glycol diacrylate, 1,4 butanediol diacrylate, diethylene glycol diacrylate, 1,6 hexanediol diacrylate, neopentyl glycol diacrylate, polyethylene glycol diacrylate, tetraethylene glycol diacrylate, triethylene glycol diacrylate, dipropylene glycol diacrylate, tripropylene glycol diacrylate, polyethylene glycol diacrylate, ethoxylated bisphenol A diacrylate, propoxylated neopentyl glycol diacrylate, ethoxylated neopentyl glycol diacrylate, ethoxylated tripropylene glycol diacrylate, and / or monomethoxytrimethylolpropane ethoxylate diacrylate.

[0037] The following triacrylates can be used: trimethylolpropane triacrylate, tris(2-hydroxyethyl)isocyanurate triacrylate, ethoxylated trimethylolpropane triacrylate, propoxylated glycerol triacrylate ditrimethylolpropane triacrylate, pentaerythritol triacrylate, and / or propoxylated trimethylolpropane triacrylate.

[0038] However, preferred polyacrylates (especially as photopolymerization reactive compounds (N) containing at least two acryloyl groups) are trimethylolpropane triacrylate, tricyclodecane dimethanol diacrylate (CAS: 42594-17-2), polyethylene glycol diacrylate (CAS: 25322-68-3), polypropylene glycol diacrylate (CAS: 52496-08-9), poly(propylene glycol) dimethacrylate (CAS: 25852-47- 5), dipropylene glycol diacrylate (CAS: 57472-68-1), trimethylolpropane trimethacrylate (3290-92-4), bisphenol A glycerolate diacrylate (CAS: 4687-94-9), tris isocyanurate triacrylate (CAS: 40220-08-4), bisphenol A epoxy diacrylate (CAS: 55818-57-0), and / or trimethylolpropane tetraacrylate (CAS: 94108-97-1).

[0039] The one or more photocurable compounds are included in the inkjet composition in the molar amounts specified above, which may be, for example, an amount of 20 to 50% by weight, based on the total weight of the inkjet composition.

[0040] The photopolymerization reactive compounds ((M) and (N) species) and the radical photoinitiator (R) may be included in the inkjet composition in a weight ratio of 95:5 to 99.5:0.5, preferably 97:3 to 99: 1. The photoinitiator (R) generates reactive species (free radicals) when exposed to radiation (e.g., UV light or visible light).

[0041] The photoinitiator may be included in the inkjet composition in an amount of 0.2 to 4% by weight, based on the total weight of the inkjet composition.

[0042] According to one embodiment, the radical photoinitiator (R) species is provided by a phosphine oxide based photoinitiator, preferably by diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide and / or phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide.

[0043] The thermosetting compound contained is a compound capable of addition polymerization (polyaddition) and / or crosslinking when exposed to heat. Preferably, the thermosetting compound does not polymerize and / or crosslink at temperatures below 100° C. According to the present invention, an isocyanate compound (D) containing at least two isocyanate groups is provided as the thermosetting compound.

[0044] With regard to the quality achieved (especially the mechanical properties), it is important that there is a suitable ratio of the inject composition with respect to the photoreactive groups (pre-cure for the first step) on the one hand, and the thermoreactive groups (post-cure activity) on the other hand. In this regard, preferably, in the inkjet composition, the molar ratio of the acryloyl groups contained therein to the isocyanate groups contained in the compound (D) is 1.0 to 3.0.

[0045] The isocyanate compound (D) containing at least two isocyanate groups is contained in the inkjet composition in the amount specified above (indirectly specified by the molar ratio of the acryloyl groups contained therein to the isocyanate groups contained in the compound (D)), and the amount may be, for example, 25 to 50% by mass based on the total mass of the inkjet composition.

[0046] Such isocyanate compounds (D) containing at least two isocyanate groups are well known to those skilled in the art. Related species are known as polyisocyanates and may be aliphatic or aromatic polyisocyanates (preferably diisocyanates) and / or blocked aliphatic or aromatic polyisocyanates of such.

[0047] For the sake of clarity, the aliphatic or aromatic polyisocyanates can be used in free or blocked form. However, according to a preferred embodiment, at least 90 mol %, preferably at least 99 mol %, of the species (D) are provided in fully blocked form (all isocyanate groups are blocked), whereby ε-caprolactam is preferably used as a blocking group. According to a particularly preferred embodiment, at least 90 mol %, preferably at least 99 mol %, of the species (D) are provided by fully blocked (both isocyanate groups are blocked) diisocyanates, whereby ε-caprolactam is preferably used as a blocking group.

[0048] The aliphatic or aromatic polyisocyanate may preferably comprise a tolylene diisocyanate such as 2,4-tolylene diisocyanate or 4,4-tolylene diisocyanate; a diphenylmethane diisocyanate such as 4,4-diphenylmethane diisocyanate; isophorone diisocyanate; a dicyclohexylmethane diisocyanate such as dicyclohexylmethane-4,4-diisocyanate; a hexamethylene diisocyanate such as hexamethylene-1,6-diisocyanate; or a cyclohexyl diisocyanate such as 1,4-cyclohexyl diisocyanate. Preferably, it is an aromatic polyisocyanate such as a tolylene diisocyanate such as 2,4-tolylene diisocyanate or 4,4-tolylene diisocyanate; a diphenylmethane diisocyanate such as 4,4-diphenylmethane diisocyanate; or a mixture thereof.

[0049] According to a preferred thermal reaction (post-cure) mechanism, the (thermally deblocked) isocyanate groups react with hydroxyl groups by generating urethane groups. The associated hydroxyl groups can be partially provided by hydroxyacrylates (e.g. hybrid compounds of (N) and / or (M) containing acryloyl and hydroxyl groups), but it is generally not preferred to provide said hydroxyl groups using such hybrid compounds. Generally, hybrid compounds containing (blocked) isocyanate and hydroxyl groups can also be (partially) used. However, such compounds are generally not preferred.

[0050] According to a preferred embodiment, the molar ratio of the hydroxyl groups contained in compound (H) to the isocyanate groups contained in compound (D) is 0.8 to 2.0, preferably 1.0 to 1.5 (for said ratio, possible species containing at least two isocyanate groups and further containing at least one hydroxyl group are included in (D)). In many cases, it is preferable to use a corresponding equimolar ratio (about 1:1) or to use a small excess of the hydroxyl groups of compound (H).

[0051] Typically, at least 60 mol%, preferably at least 90 mol%, of the hydroxyl groups contained are provided by species (H) (which are diols) that have exactly two (not more than two and not less than two) hydroxyl groups. However, polyols with more than two hydroxyl groups can also be used. Species that can be used are, for example, 1,3-propanediol, 1,4-butanediol, 1,6-hexanediol, hydroquinone, trimethylolpropane, glycerin, 2-phenyl alcohol and / or polypropylene glycol. However, monools (containing exactly one hydroxyl group) can also be used (usually only partially), which can be, for example, of the polyethylene glycol type.

[0052] When blocked isocyanate species are used (typically the case), the relevant species must be deblocked (thermally) prior to reaction with the diol. During photopolymerization (first step), these blocked species are inactive and must be deblocked to react (preferably at higher temperatures) in the post-cure step.

[0053] Blocking of the thermosetting compound (preferably an aliphatic or aromatic polyisocyanate) results in a latent reactive functional group, which is released after deblocking of the blocking agent and can further react with additional reactive functional groups. Thereby, the blocking agent reacts with the thermosetting compound (preferably an aliphatic or aromatic polyisocyanate) to covalently bond the blocking agent to the reactive group of the thermosetting compound (the isocyanate group of the aliphatic or aromatic polyisocyanate). Deblocking of the thermosetting compound can be preferably achieved by heating.

[0054] Preferably, the blocking agent may be selected from the group consisting of caprolactam, preferably ε-caprolactam, methyl ketone oxime, imidazole, 3,5-dimethylpyrazole or diisopropylamine. Preferably, the blocking agent may be selected from ε-caprolactam, methyl ketone oxime, imidazole or 3,5-dimethylpyrazole, more preferably ε-caprolactam. ε-caprolactam has the advantage that it is not volatile and therefore remains in the body even during the thermal curing process. Volatile protecting groups can usually cause problems in this regard (e.g. caused by undesirable bubbling).

[0055] The blocking agent is usually present in an amount such that at least about 90% of the reactive groups of the thermosetting compound are blocked, preferably at least about 99%, and most preferably to the extent of 100% of the isocyanates.

[0056] In practice, solubility and overall compatibility in UV systems can be an issue for blocked isocyanates, so UV systems for related polyurethane materials are also designed (as discussed above) to avoid phase separation.

[0057] When blocking groups are provided, it is not necessary to use a curing catalyst because at the high "unblocking temperatures" involved the thermal curing reaction (urethane formation) works well without a catalyst. However, the curing temperature should not be too high, as UV systems may not be able to withstand temperatures above 220°C for extended periods of time.

[0058] According to a preferred embodiment, 90 to 100% by weight, preferably 97 to 100% by weight, of the components contained (in the inkjet composition) are provided by the species (M), (N), (R), (D), and (H).

[0059] The addition of other components is possible, but in many cases is not advantageous (e.g. if there is no contribution in terms of the curing effect or if undesirable thermal reactivity occurs below 100° C.): It is usually not preferred to use (relatively high amounts) of inert solvents (which cannot be photopolymerized in a first step or post-cured in a second step). Preferably, the inkjet composition contains less than 8% by weight, more preferably less than 2% by weight of inert solvent. Furthermore, it is not preferred to use (relatively high amounts) of radically polymerizable monomers (such as methacrylates) that do not contain acryloyl groups. Preferably, the inkjet composition contains less than 6% by weight, more preferably less than 2% by weight of radically polymerizable monomers that do not contain acryloyl groups. For example, methacrylates are not sufficiently reactive for (short) radical photopolymerization, for example. Preferably, the inkjet composition contains less than 6% by weight, more preferably less than 2% by weight of methacrylates (which do not contain acryloyl groups).

[0060] In order to avoid undesirable side reactions (which typically increase the viscosity), the inkjet composition preferably does not contain cationic (photo)initiators and / or anionic (photo)initiators. In any case, it is preferable to avoid compounds (especially high amounts of compounds) that react in the composition via one of the step-reaction types (polyaddition, polycondensation) at temperatures below 100°C. Such compounds (especially relatively high amounts of such compounds) may cause problems with the desired viscosity stability. To enable jetting through a narrow nozzle, it is necessary to limit the viscosity of the inkjet composition.

[0061] However, the inkjet composition according to the present invention may further contain a stabilizer, a wetting agent, a radical polymerization inhibitor, a defoamer, and / or a pigment. Usually, dissolved oxygen acts as a radical polymerization inhibitor, but a synthesis inhibitor may be used in addition.

[0062] Typically, the inkjet composition has a viscosity of 10 to 150 mPa.s at 45° C., where the viscosity is measured on a thermally controlled rotational rheometer in cone-plate geometry (Anton Paar Physica MCR 300, cone diameter: 60 mm, zero-gap distance: 0.061 mm, cone angle: 0.5°, shear rate: 600 s -1 ).

[0063] The present invention further relates to a method for printing a three-dimensional object, comprising the steps of: (a) jetting the ink jet composition by a printer to form a layer in a structured pattern corresponding to the shape of an object; (b) irradiating the formed layer to form a photohardened layer; (c) sequentially repeating steps (a) and (b) to form a plurality of photocured layers to prepare a green body of the three-dimensional object; and (d) heating the green body to post-cure the three-dimensional object.

[0064] Typically, in order to stabilise the green body, a supporting ink is further printed and cured, this cured supporting ink being water-soluble and being removed after step c) and before carrying out step (d) by treatment with an aqueous washing liquid.

[0065] Typically, step (d) is carried out such that a temperature of 140-190° C. is maintained for at least 1 hour.

[0066] Typically, in the heating step (d), the associated temperature increase is limited to 2 K / min.

[0067] Preferably, in step (b), the irradiation is carried out by a UV lamp, and the exposure time of each ink layer is 0.1-2 seconds.

[0068] A typical procedure may be as follows: The inkjet composition can be filtered before it is used as an inkjet composition. Preferably, the inkjet composition is filtered so as not to contain particles with a particle size greater than 1 μm. The ink is then placed in the printer. The system is recirculated for at least 2 hours, and better more, to ensure uniformity and constant temperature. During printing, the support ink (e.g., acrylamide-based) is inkjetted and UV-cured to generate a mold for the object ink, which is later inkjetted and UV-cured (wet-on-dry printing). To control the layer thickness, all the inks are leveled once in their liquid state on the build tray, which occurs after the ink jetting during the dynamic wetting process on the substrate and before UV-curing. In this way, a 3D object is generated. Since the support ink is printed layer by layer (together with the layers of the green body), after the printing process the object (green body) becomes surrounded by the support material (e.g., polyacrylamide). To remove the support material, the entire structure is placed in a water bath and heated to 35-40 ° C in the presence of ultrasound. Depending on the support material and the geometry of the object, the cleaning process can take anywhere from 0.5 hours to 24 hours (sometimes longer). Once all support structures have been removed, the object is removed from the water bath and allowed to air dry at room temperature. After about 5 hours of drying, the object is placed in a heating chamber (a type of oven) and a well-suited temperature program is selected depending on the chemistry, geometry and application to thermally cure the thermosetting system present in the printed and now washed object.

[0069] The present invention further relates to a three-dimensional object produced according to the above method.

[0070] The three-dimensional object may have a tensile strength of 0.5-25 MPa, preferably 2-20 MPa, and an elongation at break of 15-100%, preferably greater than 100%, and an E-modulus of 1-1000 MPa, preferably 10-200 MPa.

[0071] Additionally, the present invention relates to the use of the above ink-jet composition for producing a three-dimensional object.

[0072] General measurement method The viscosity was measured using a thermally controlled rotational rheometer with cone-plate geometry (Anton Paar Physica MCR 300, cone diameter: 60 mm, zero-gap distance: 0.061 mm, cone angle: 0.5°, shear rate: 600 s -1 ) at temperatures between 40 and 60 °C at a heating rate of 2 K / min according to DIN EN ISO 3219. For comparison, the viscosity at 50 °C is shown in the examples below. The storage stability of the inks was determined in the same experiments as above after storing closed sample jars at 60 or 80 °C for 7 days.

[0073] The Shore hardness A and D were measured using a cylindrical specimen with a diameter of 40 mm and a thickness of 7 mm with an OS-2 measuring device (Hildebrand Pruf- und Messtechnik GmbH) according to DIN EN ISO standard 7619. The results were taken from the scale 3 seconds after the needle had entered the specimen. The measurements were repeated 5 times.

[0074] Tensile tests were performed with 5A specimens according to DIN EN ISO standard 527-1 on a Zwick-Roell tensile testing machine 1445. The E-modulus was determined from the slope of the stress-strain curve at a deformation of 0.05-0.25% at 1 mm / min. The tensile strength and elongation at break were determined by pulling the specimens at 25 mm / min for elastic samples.

[0075] The invention is further explained below by means of examples.

[0076] General Terms and Definitions Reactants used in the examples - Isobornyl acrylate (IBOA): CAS No 5888-33-5, SARTOMER - Acryloylmorpholine (ACMO): CAS No 5117-12-4, RAHN - Trimethylolpropane triacrylate (TMPTA): CAS No 15625-89-5, SARTOMER - Polyethylene glycol 600 diacrylate (PEG600DA, Miramer M286): CAS No 26570-48-9, MIWON - 2-[[(Butylamino)carbonyl]oxy]ethyl acrylate (Genomer 1122tf) - CAS No 63225-53-6, RAHN - Dipropylene glycol diacrylate (DPGDA, Miramer M222): CAS No 57472-68-1, MIWON - Omnirad 819: Photoinitiator with CAS No 162881-26-7, IGM Resins - Genorad 16: A polymerization inhibitor that is a combination of glycerol propoxylate (1PO / OH) and 4-methoxyphenol, RAHN - BYK 333: Polyether modified polydimethylsiloxane additive, BYK - K-KAT™ XK-651: Bismuth carboxylate catalyst, King Industries - DESMSODUR N3400: Hexamethylene diisocyanate, CAS No. 28182-81-2, COVESTRO - ε-Caprolactam, CAS No. 105-60-2, SIGMA ALDRICH - Isophorone diisocyanate (IPDI), CAS No. 4098-71-9, SIGMA ALDRICH - DESMODUR BL3272: ε-caprolactam blocked aliphatic polyisocyanate (CAS No 26776-30-7) based on HDI (28% in 1-methoxypropyl acetate-2 (MPA CAS No 108-65-6)), COVESTRO - DESMODUR BL3175: Butanone oxime blocked aliphatic polyisocyanate based on HDI (CAS No 85940-94-9) (25% in Solvent Naphtha 100 (SN CAS No 64742-95-6)), COVESTRO - DESMODUR BL3575-1: 3,5-dimethylpyrazole blocked aliphatic polyisocyanate based on HDI (CAS No 163206-31-3) (25% in 1-methoxypropyl acetate-2 / solvent naphtha 100 8:17), COVESTRO - DESMODUR BL3475: Diethyl malonate blocked aliphatic polyisocyanate based on HDI / IPDI (DEM CAS No 105-53-3) (25% in n-butyl acetate / solvent naphtha 100 1:1 (CAS No 123-86-4)), COVESTRO - 1,3-Propanediol: CAS No 504-63-2, SIGMA ALDRICH - 1,6-Hexanediol: CAS No 629-11-8, SIGMA ALDRICH - Polytetrahydrofuran 250 (pTHF250): CAS No 25190-06-1, SIGMA ALDRICH - Polypropylene glycol 400 (PPG400): CAS No 25322-69-4, SIGMA ALDRICH - Polyethylene glycol 600 (PEG600): CAS No 25322-68-3, SIGMA ALDRICH

[0077] Example 1: Synthesis of blocked isocyanate BI 1 Hexamethylene diisocyanate (DESMODUR N3400; 304.99 g; 2.92 mol; 1 eq.) was mixed with K-KAT™ (XK-651 (KING INDUSTRIES, bismuth-carboxylate based; 4.4 g; 0.94 wt.%) in a four-neck reactor (2500 mL) and stirred at 50° C. for 30 min. Then, ε-caprolactam (165.18 g; 1.46 mol; 2 eq.) was added at 50° C. and further stirred at 60° C. for 3.5 h.

[0078] Synthesis of Inkjet Compositions Isobornyl acrylate (34.5% by weight), polyethylene glycol 600 diacrylate (PEG 600 DA) (12.0% by weight), 2-[[(butylamino)carbonyl]oxy]ethyl acrylate (Genomer 1122tf) (12.0% by weight), Omnirad 819 (1.2% by weight), Genorad 16 (0.15% by weight), BYK 333 (0.18% by weight), 1,6-hexanediol (10.9% by weight), and the above synthesized blocked isocyanate compound BI 1 (29.0% by weight) were mixed and filtered at 1 μm. The ink was inkjet UV printed and post-cured at 130 °C for 10 minutes.

[0079] The final properties of the final object were: Maximum tensile strength: 7MPa Elongation at break: 100% E-elastic modulus: 20MPa

[0080] The viscosity stability of Example 1 is measured as follows: [Table 1] [Table 2]

[0081] The inkjet composition comprises: (I) Mol / kg of acryloyl groups in (M) and (N): 2.61 (II) Mol% of acryloyl groups provided by reactive compound (N): 15.3 (III) Molar ratio of the acryloyl groups (M) and (N) contained in the compound (D) to the isocyanate groups contained in the compound (D): 1.27

[0082] Examples 2-14: To screen the ink and material properties of potential inkjet formulations, the molded specimens were placed in a translucent silicone mold at a distance of 15 cm from the bottom and illuminated with UV light (LED 395 nm, 16 W / cm 2 ) for 30 seconds on each side. A thermal post-cure is then performed. Thus, the photopolymerized and oven-cured bulk specimen test results closely highlight the final material performance of the jetted material and the post-cured formulation, despite the different preparation processes in the first cure step of the interpenetrating system. Examples 2-14 show various blend ratios of different acrylates, blocked isocyanates, and polyol compounds to highlight the correlation between printing applications and material properties.

[0083] Example 2: Isobornyl acrylate (18.0 wt%), acryloylmorpholine (18.5 wt%), (12.0 wt%), trimethylpropane triacrylate (5.3 wt%), Omnirad 819 (0.13 wt%), Genorad 16 (0.09 wt%), 1,6-hexanediol (15.9 wt%), and the above synthesized blocked isocyanate compound BI 1 (42.1 wt%) were mixed. Inks were cast as above and post-cured at 180° C. for 1 hour.

[0084] The final properties of the final object were: Maximum tensile strength: 17MPa Elongation at break: 15% E-elastic modulus: 600MPa Hardness (after heat curing): A86

[0085] The viscosity stability of Example 2 is measured as follows: [Table 3] [Table 4]

[0086] The inkjet composition comprises: (I) Mol / kg of acryloyl groups in (M) and (N): 2.71 (II) Mol% of acryloyl groups provided by reactive compound (N): 19.8 (III) Molar ratio of the acryloyl groups (M) and (N) contained in the compound (D) to the isocyanate groups contained in the compound (D): 0.91

[0087] Example 3: Isobornyl acrylate (36.5% by weight), acryloylmorpholine (6.3% by weight), Glycol 600 diacrylate (6.3% by weight), dipropylene glycol diacrylate (0.5% by weight), Omnirad 819 (0.15% by weight), Genorad 16 (0.13% by weight), 1,6-hexanediol (13.8% by weight), and the previously synthesized blocked isocyanate compound BI 1 (36.3% by weight) were mixed. Inks were cast as described above and post-cured at 180° C. for 1 hour.

[0088] The final properties of the final object were: Maximum tensile strength: 14MPa Elongation at break: 61% E-elastic modulus: 300MPa Hardness (after heat curing): A90

[0089] The viscosity stability of Example 3 is measured as follows: [Table 5] [Table 6]

[0090] The inkjet composition comprises: (I) Mol / kg of acryloyl groups in (M) and (N): 2.44 (II) Mol% of acryloyl groups provided by reactive compound (N): 10.2 (III) Molar ratio of the acryloyl groups (M) and (N) contained in the compound (D) to the isocyanate groups contained in the compound (D): 0.95

[0091] Example 4: Isobornyl acrylate (38.5% by weight), Glycol 600 diacrylate (12.7% by weight), dipropylene glycol diacrylate (0.5% by weight), Omnirad 819 (0.16% by weight), Genorad 16 (0.1% by weight), 1,6-hexanediol (13.2% by weight), and the previously synthesized blocked isocyanate compound BI 1 (34.9% by weight) were mixed. Inks were cast as above and post-cured at 180° C. for 1 hour.

[0092] The final properties of the final object were: Maximum tensile strength: 12MPa Elongation at break: 87% E-elastic modulus: 50MPa Hardness (after heat curing): A86

[0093] The viscosity stability of Example 4 is measured as follows: [Table 7] [Table 8]

[0094] The inkjet composition comprises: (I) Mol / kg of acryloyl groups in (M) and (N): 2.31 (II) Mol% of acryloyl groups provided by reactive compound (N): 20.2 (III) Molar ratio of the acryloyl groups (M) and (N) contained in the compound (D) to the isocyanate groups contained in the compound (D): 0.93

[0095] Example 5: Isobornyl acrylate (30.2% by weight), Glycol 600 diacrylate (10.4% by weight), 2-[[(butylamino)carbonyl]oxy]ethyl acrylate (Genomer 1122tf) (10.4% by weight), Omnirad 819 (0.16% by weight), Genorad 16 (0.1% by weight), 1,6-hexanediol (13.2% by weight), and the previously synthesized blocked isocyanate compound BI 1 (34.9% by weight) were mixed. Inks were cast as described above and post-cured at 180° C. for 1 hour.

[0096] The final properties of the final object were: Maximum tensile strength: 5MPa Elongation at break: 110% E-elastic modulus: 1MPa Hardness (after heat curing): A80 [Table 9]

[0097] The inkjet composition comprises: (I) Mol / kg of acryloyl groups in (M) and (N): 2.28 (II) Mol% of acryloyl groups provided by reactive compound (N): 15.2 (III) Molar ratio of the acryloyl groups (M) and (N) contained in the compound (D) to the isocyanate groups contained in the compound (D): 0.92

[0098] Example 6: Isobornyl acrylate (34.5% by weight), Glycol 600 diacrylate (12.0% by weight), 2-[[(butylamino)carbonyl]oxy]ethyl acrylate (Genomer 1122tf) (12.0% by weight), Omnirad 819 (0.18% by weight), Genorad 16 (0.12% by weight), 1,3-propanediol (7.8% by weight), and the previously synthesized blocked isocyanate compound BI 1 (32.2% by weight) were mixed. Inks were cast as above and post-cured at 180° C. for 1 hour.

[0099] The final properties of the final object were: Maximum tensile strength: 4MPa Elongation at break: 96% E-elastic modulus: 1MPa Hardness (after UV curing): A41 Hardness (after heat curing): A67

[0100] The viscosity stability of Example 6 is measured as follows: [Table 10] [Table 11]

[0101] The inkjet composition comprises: (I) Mol / kg of acryloyl groups in (M) and (N): 2.61 (II) Mol% of acryloyl groups provided by reactive compound (N): 15.3 (III) Molar ratio of the acryloyl groups (M) and (N) contained in the compound (III) to the isocyanate groups contained in the compound (D): 1.14

[0102] Example 7: Isobornyl acrylate (34.5% by weight), Glycol 600 diacrylate (12.0% by weight), 2-[[(butylamino)carbonyl]oxy]ethyl acrylate (Genomer 1122tf) (12.0% by weight), Omnirad 819 (0.18% by weight), Genorad 16 (0.12% by weight), polytetrahydrofuran 250 (17.8% by weight), and the previously synthesized blocked isocyanate compound BI 1 (22.2% by weight) were mixed. Inks were cast as described above and post-cured at 180° C. for 1 hour.

[0103] The final properties of the final object were: Maximum tensile strength: 2MPa Elongation at break: 78% E-elastic modulus: 1MPa Hardness (after UV curing): A31 Hardness (after heat curing): A50

[0104] The viscosity stability of Example 7 is measured as follows: [Table 12] [Table 13]

[0105] The inkjet composition comprises: (I) Mol / kg of acryloyl groups in (M) and (N): 2.61 (II) Mol% of acryloyl groups provided by reactive compound (N): 15.3 (III) Molar ratio of the acryloyl groups (M) and (N) contained in the compound (D) to the isocyanate groups contained in the compound (D): 1.65

[0106] Example 8: Isobornyl acrylate (34.5% by weight), Glycol 600 diacrylate (12.0% by weight), 2-[[(butylamino)carbonyl]oxy]ethyl acrylate (Genomer 1122tf) (12.0% by weight), Omnirad 819 (0.18% by weight), Genorad 16 (0.12% by weight), Polypropylene glycol 400 (22.5% by weight), and the previously synthesized blocked isocyanate compound BI 1 (17.5% by weight) were mixed. Inks were cast as described above and post-cured at 180° C. for 1 hour.

[0107] The final properties of the final object were: Maximum tensile strength: 1MPa Elongation at break: 71% E-elastic modulus: 2MPa Hardness (after UV curing): A17 Hardness (after heat curing): A40

[0108] The viscosity stability of Example 8 is measured as follows: [Table 14] [Table 15]

[0109] The inkjet composition comprises: (I) Mol / kg of acryloyl groups in (M) and (N): 2.61 (II) Mol% of acryloyl groups provided by reactive compound (N): 15.3 (III) Molar ratio of the acryloyl groups (M) and (N) contained in the compound (D) to the isocyanate groups contained in the compound (D): 2.09

[0110] Example 9: Isobornyl acrylate (34.5% by weight), Glycol 600 diacrylate (12.0% by weight), 2-[[(butylamino)carbonyl]oxy]ethyl acrylate (Genomer 1122tf) (12.0% by weight), Omnirad 819 (0.18% by weight), Genorad 16 (0.12% by weight), polyethylene glycol 600 (26.3% by weight), and the previously synthesized blocked isocyanate compound BI 1 (13.7% by weight) were mixed. Inks were cast as described above and post-cured at 180° C. for 1 hour.

[0111] The final properties of the final object were: Maximum tensile strength: 2MPa Elongation at break: 92% E-elastic modulus: 1MPa Hardness (after UV curing): A53 Hardness (after heat curing): A61

[0112] The viscosity stability of Example 9 is measured as follows: [Table 16] [Table 17]

[0113] The inkjet composition comprises: (I) Mol / kg of acryloyl groups in (M) and (N): 2.61 (II) Mol% of acryloyl groups provided by reactive compound (N): 15.3 (III) Molar ratio of the acryloyl groups (M) and (N) contained in the compound (D) to the isocyanate groups contained in the compound (D): 2.68

[0114] Example 10: Synthesis of blocked isocyanate Bl 2 Isophorone diisocyanate (56.34 g; 253.3 mmol; 2 eq.) was mixed with KKAT™ XK-651 (KING INDUSTRIES, bismuth-carboxylate based; 1.0 g; 1.0 wt.%) in a four-neck reactor (2500 mL) and stirred at 50° C. for 5 min. 1,6-Hexanediol (14.99 g, 126.8 mmol, 1 eq.) was carefully melted and then added dropwise in a 5 min time frame such that the reaction temperature did not exceed 75° C. The reaction mixture was further stirred at 50° C. for 3.5 h. ε-caprolactam (27.73 g; 425.1 mmol; 2 eq.) was then added at 70° C. and further stirred at 70° C. for 3 h.

[0115] Synthesis of Inkjet Compositions Isobornyl acrylate (36.9% by weight), Glycol 600 diacrylate (12.3% by weight), dipropylene glycol diacrylate (0.5% by weight), Omnirad 819 (0.15% by weight), Genorad 16 (0.1% by weight), BYK333 (0.13% by weight), polyethylene glycol 600 (22.8% by weight), and the above synthesized blocked isocyanate compound BI 2 (27.2% by weight) were mixed. Inks were cast as above and post-cured at 180° C. for 1 hour.

[0116] The final properties of the final object were: Maximum tensile strength: 2MPa Elongation at break: 31% E-elastic modulus: 13MPa

[0117] The viscosity stability of Example 10 is measured as follows: [Table 18] [Table 19]

[0118] The inkjet composition comprises: (I) Mol / kg of acryloyl groups in (M) and (N): 2.22 (II) Mol% of acryloyl groups provided by reactive compound (N): 20.3 (III) Molar ratio of the acryloyl groups (M) and (N) contained in the compound (III) to the isocyanate groups contained in the compound (D): 3.21

[0119] Example 11: Isobornyl acrylate (36.9% by weight), Glycol 600 diacrylate (12.3% by weight), dipropylene glycol diacrylate (0.5% by weight), Omnirad 819 (0.15% by weight), Genorad 16 (0.1% by weight), polytetrahydrofuran (10.7% by weight), and Desmodur BL3272 (39.3% by weight) were mixed. The ink was cast as above and post-cured at 180° C. for 1 hour.

[0120] The final properties of the final object were: Maximum tensile strength: 7MPa Elongation at break: 79% E-elastic modulus: 60MPa Hardness (after UV curing): A24 Hardness (after heat curing): A64

[0121] The viscosity stability of Example 11 is measured as follows: [Table 20] [Table 21]

[0122] The inkjet composition comprises: (I) Mol / kg of acryloyl groups in (M) and (N): 2.22 (II) Mol% of acryloyl groups provided by reactive compound (N): 20.3 (III) Molar ratio of the acryloyl groups (M) and (N) contained in the compound (D) to the isocyanate groups contained in the compound (D): 2.20

[0123] Example 12: Isobornyl acrylate (36.9% by weight), Glycol 600 diacrylate (12.3% by weight), dipropylene glycol diacrylate (0.5% by weight), Omnirad 819 (0.15% by weight), Genorad 16 (0.1% by weight), polytetrahydrofuran (11.5% by weight), and Desmodur BL3175 (38.5% by weight) were mixed. The ink was cast as above and post-cured at 170° C. for 1 hour.

[0124] The final properties of the final object were: Maximum tensile strength: 2MPa Elongation at break: 110% E-elastic modulus: 1MPa Hardness (after heat curing): A22

[0125] The viscosity stability of Example 12 is measured as follows: [Table 22] [Table 23]

[0126] The inkjet composition comprises: (I) Mol / kg of acryloyl groups in (M) and (N): 2.22 (II) Mol% of acryloyl groups provided by reactive compound (N): 20.3 (III) Molar ratio of the acryloyl groups (M) and (N) contained in the compound (D) to the isocyanate groups contained in the compound (D): 1.96

[0127] Example 13: Isobornyl acrylate (36.9% by weight), Glycol 600 diacrylate (12.3% by weight), dipropylene glycol diacrylate (0.5% by weight), Omnirad 819 (0.15% by weight), Genorad 16 (0.1% by weight), polytetrahydrofuran (11.0% by weight), and Desmodur BL3575-1 (39.0% by weight) were mixed. The ink was cast as above and post-cured at 150° C. for 1 hour.

[0128] The final properties of the final object were: Maximum tensile strength: 4MPa Elongation at break: 140% E-elastic modulus: 1MPa Hardness (after heat curing): A28

[0129] The viscosity stability of Example 13 is measured as follows: [Table 24] [Table 25]

[0130] The inkjet composition comprises: (I) Mol / kg of acryloyl groups in (M) and (N): 2.22 (II) Mol% of acryloyl groups provided by reactive compound (N): 20.3 (III) Molar ratio of the acryloyl groups (M) and (N) contained in the compound (D) to the isocyanate groups contained in the compound (D): 2.00

[0131] Example 14: Isobornyl acrylate (36.9% by weight), Glycol 600 diacrylate (12.3% by weight), dipropylene glycol diacrylate (0.5% by weight), Omnirad 819 (0.15% by weight), Genorad 16 (0.1% by weight), polytetrahydrofuran (9.0% by weight), and Desmodur BL3475 (41.0% by weight) were mixed. The ink was cast as above and post-cured at 140° C. for 1 hour.

[0132] The final properties of the final object were: Maximum tensile strength: 2MPa Elongation at break: 110% E-elastic modulus: 1MPa Hardness (after heat curing): A25

[0133] The viscosity stability of Example 14 is measured as follows: [Table 26]

[0134] The stability of this inkjet ink containing the blocking agent diethyl malonate at 60° C. is determined to be too low to allow further processing of the ink. [Table 27]

[0135] The inkjet composition comprises: (I) Mol / kg of acryloyl groups in (M) and (N): 2.22 (II) Mol% of acryloyl groups provided by reactive compound (N): 20.3 (III) Molar ratio of the acryloyl groups (M) and (N) contained in the compound (D) to the isocyanate groups contained in the compound (D): 1.18 The present disclosure also includes the following: <Aspect 1> An inkjet composition having 1.8 to 3.3 mol / kg of acryloyl groups, the inkjet composition comprising: (i) a photopolymerizable reactive compound (M) containing exactly one acryloyl group; (ii) a photopolymerization reactive compound (N) containing at least two acryloyl groups; (iii) a radical photoinitiator (R); (iv) an isocyanate compound (D) containing at least two isocyanate groups, and (v) Compounds (H) containing at least one hydroxyl group Including, The (M) is different from the (D), except that an isocyanate compound containing exactly one acryloyl group and further containing at least two isocyanate groups should be included in the (D); The (N) is different from the (D), except that an isocyanate compound containing at least two acryloyl groups and further containing at least two isocyanate groups should be included in the (D); (H) is different from (D), (M), and (N); The ink-jet composition, wherein 10 to 28 mol % of the acryloyl groups contained therein are provided by the reactive compound (N), and the molar ratio of the acryloyl groups contained therein to the isocyanate groups contained in the compound (D) is 0.9 to 3.3. <Aspect 2> The inkjet composition according to embodiment 1, having 2.0 to 3.0 mol / kg of acryloyl groups. <Aspect 3> The ink-jet composition according to the above-mentioned embodiment 1 or 2, wherein 10 to 25 mol % of the contained acryloyl groups are provided by the reactive compound (N). <Aspect 4> The inkjet composition according to any one of Aspects 1 to 3 above, wherein 90 to 100 mol %, preferably 95 to 100 mol %, of the reactive compound (N) is provided by a species containing three or less acryloyl groups. <Aspect 5> The ink-jet composition according to any one of the above-mentioned embodiments 1 to 4, wherein the molar ratio of the acryloyl group contained in the compound (D) to the isocyanate group contained in the compound (D) is 1.0 to 3.0. <Aspect 6> 6. The inkjet composition according to any one of Aspects 1 to 5 above, wherein the species of the radical photoinitiator (R) is provided by a phosphine oxide based photoinitiator, preferably by diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide, and / or phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide. <Aspect 7> The inkjet composition according to any one of Aspects 1 to 6, wherein at least 90 mol % of the species of (D), preferably at least 99 mol % of the species of (D) is provided in a completely blocked form (all isocyanate groups are blocked), and preferably ε-caprolactam is used as the blocking group. <Aspect 8> The inkjet composition according to any one of the above-mentioned aspects 1 to 7, wherein the molar ratio of the hydroxyl group contained in the compound (H) to the isocyanate group contained in the compound (D) is 0.8 to 2.0, and preferably 1.0 to 1.5. <Aspect 9> The inkjet composition according to any one of Aspects 1 to 8 above, wherein at least 60 mol %, preferably at least 90 mol %, of the hydroxyl groups contained therein are provided by the (H) species having exactly two hydroxyl groups (being a diol). <Aspect 10> The inkjet composition according to any one of Aspects 1 to 9, wherein 90 to 100% by mass, and preferably 97 to 100% by mass, of the components contained therein are provided by the species of (M), (N), (R), (D), and (H). <Aspect 11> The viscosity is measured using a thermally controlled rotational rheometer with cone-plate geometry (cone diameter: 60 mm, zero-gap distance: 0.061 mm, cone angle: 0.5°, shear rate: 600 s -1 11. The inkjet composition according to any one of Aspects 1 to 10, wherein the viscosity is measured according to DIN EN ISO 3219 at a temperature of 40 to 60° C. with a heating rate of 2 K / min. <Aspect 12> The ink-jet composition according to any one of the above-mentioned aspects 1 to 11, which does not contain a cationic (photo)polymerization initiator or an anionic (photo)polymerization initiator. <Aspect 13> 13. The inkjet composition according to any one of the above embodiments 1 to 12, comprising less than 6% by mass, more preferably less than 2% by mass, of a radically polymerizable monomer not containing an acryloyl group. <Aspect 14> 14. The ink jet composition according to any one of the above embodiments 1 to 13, further comprising a stabilizer, a wetting agent, a radical polymerization inhibitor, a defoamer, and / or a pigment. <Aspect 15> Next steps: (a) spraying the ink jet composition according to any one of the above embodiments 1 to 14 with a printer to form a layer having a structural pattern corresponding to the shape of an object; (b) irradiating the formed layer to form a photohardened layer; (c) sequentially repeating steps (a) and (b) to form a plurality of photocured layers to prepare a green body of the three-dimensional object; and (d) heating the green body to post-cure the three-dimensional object. A method for printing a three-dimensional object, comprising: <Aspect 16> 16. The method of claim 15, further comprising printing and curing a support ink to stabilize the green body, the cured support ink being water-soluble and being removed after step c) and before performing step (d) by treatment with an aqueous washing liquid. <Aspect 17> 17. The method of any one of claims 15 to 16, wherein step (d) is carried out such that a temperature of 140 to 190°C is maintained for at least 1 hour. <Aspect 18> 18. The method according to any one of Aspects 15 to 17, wherein in step (b), the irradiation is performed by a UV lamp and the exposure time of each ink layer is 0.1 to 2 seconds. <Aspect 19> A three-dimensional object produced by the method according to any one of aspects 15 to 18 above. <Aspect 20> Use of the inkjet composition according to any one of the above embodiments 1 to 14 for producing a three-dimensional object.

Claims

1. An inkjet composition having 1.8 to 3.3 mol / kg of acryloyl groups, the inkjet composition comprising: (i) a photopolymerization reactive compound (M) containing exactly one acryloyl group; (ii) a photopolymerization reactive compound (N) containing at least two acryloyl groups; (iii) a radical photoinitiator (R); (iv) an isocyanate compound (D) containing at least two isocyanate groups, and v) a compound (H) containing at least one hydroxyl group Including, The (M) is different from the (D), except that an isocyanate compound containing exactly one acryloyl group and further containing at least two isocyanate groups should be included in the (D); The (N) is different from the (D), except that an isocyanate compound containing at least two acryloyl groups and further containing at least two isocyanate groups should be included in the (D); (H) is different from (D), (M), and (N); The ink-jet composition, wherein 10 to 28 mol % of the acryloyl groups contained therein are provided by the reactive compound (N), and the molar ratio of the acryloyl groups contained therein to the isocyanate groups contained in the compound (D) is 0.9 to 3.

3.

2. The ink jet composition according to claim 1, having 2.0 to 3.0 mol / kg of acryloyl groups.

3. 3. The ink-jet composition according to claim 1, wherein 10 to 25 mol % of the contained acryloyl groups are provided by the reactive compound (N).

4. 3. The ink jet composition of claim 1, wherein 90-100 mol % of the reactive compound (N) is provided by a species containing up to three acryloyl groups.

5. 3. The ink jet composition according to claim 1, wherein a molar ratio of the acryloyl group contained in the compound (D) to the isocyanate group contained in the compound (D) is from 1.0 to 3.

0.

6. The ink jet composition of claim 1 or 2, wherein the radical photoinitiator (R) species is provided by a phosphine oxide based photoinitiator.

7. 3. The ink jet composition of claim 1 or 2, wherein at least 90 mol % of the (D) species is provided in a fully blocked form (all isocyanate groups are blocked).

8. 3. The ink jet composition according to claim 1, wherein a molar ratio of a hydroxyl group contained in the compound (H) to an isocyanate group contained in the compound (D) is 0.8 to 2.

0.

9. 3. The inkjet composition of claim 1 or 2, wherein at least 60 mol % of the hydroxyl groups contained therein are provided by the (H) species having exactly two hydroxyl groups, which are diols.

10. 3. The inkjet composition according to claim 1, wherein 90 to 100 mass % of the components contained therein are provided by the species (M), the species (N), the species (R), the species (D), and the species (H).

11. 3. The ink jet composition according to claim 1 or 2, having a viscosity of 10 to 150 mPa.s at 45°C, where the viscosity is measured in a thermally controlled rotational rheometer in cone-plate geometry (cone diameter: 60 mm, zero-gap distance: 0.061 mm, cone angle: 0.5°, shear rate 600 s-1) according to DIN EN ISO 3219 at a heating rate of 2 K / min at a temperature of 40 to 60°C.

12. The ink jet composition according to claim 1 or 2, which does not contain a cationic (photo)polymerization initiator and / or an anionic (photo)polymerization initiator.

13. The ink jet composition according to claim 1 or 2, comprising less than 6% by weight of a radically polymerizable monomer not containing an acryloyl group.

14. The ink jet composition according to claim 1 or 2, further comprising a stabilizer, a wetting agent, a radical polymerization inhibitor, a defoamer, and / or a pigment.

15. Next steps: (a) jetting the ink jet composition according to claim 1 or 2 by a printer to form a layer of a structural pattern corresponding to the shape of an object; (b) irradiating the formed layer to form a photohardened layer; (c) sequentially repeating steps (a) and (b) to form a plurality of photocured layers to prepare a green body of the three-dimensional object; and (d) heating the green body to post-cure the three-dimensional object. A method for printing a three-dimensional object, comprising:

16. 16. The method of claim 15, further comprising printing and curing a supporting ink to stabilize the green body, the cured supporting ink being water-soluble and being removed after step c) and before performing step (d) by treating with an aqueous washing liquid.

17. 16. The method of claim 15, wherein step (d) is carried out such that a temperature of 140-190° C. is maintained for at least 1 hour.

18. The method according to claim 15, wherein in step (b), the irradiation is performed by a UV lamp, and the exposure time of each ink layer is 0.1 to 2 seconds.

19. A three-dimensional object manufactured by the method of claim 15.

20. Use of the ink jet composition according to claim 1 or 2 for producing a three-dimensional object.

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