Additive production process with a thermoplastic radically cross-linkable construction material
The present invention relates to a method for producing an object in an additive manufacturing process from a precursor and comprises the following steps: I) depositing a layer of a radically cross-linkable construction material, which corresponds to a first selected cross-section of the precursor, on a carrier; II) depositing a layer of a radically cross-linkable construction material, which corresponds to a further selected cross-section of the precursor, on a previously applied layer of the radically cross-linked construction material; III) repeating step II) until the precursor is formed. The radically cross-linkable construction material comprises a thermoplastic radically cross-linkable polyurethane with a urethane group content of ≥5% by weight and a photoinitiator. The radically cross-linkable construction material is also heated to a processing temperature that is greater than the melting point of the radically cross-linkable polyurethane. After step III) the precursor having a temperature of 20° C. is defined as the object, or step IV) is performed: IV) performing a chemical reaction in the precursor obtained after step III) so that the object is obtained.
1 . A method of producing an article in an additive manufacturing method from a precursor, comprising:
I) depositing a first layer of a free-radically crosslinked build material corresponding to a first selected cross section of the precursor on a carrier;
II) depositing a further layer of the free-radically crosslinked build material corresponding to a further selected cross section of the precursor onto the first layer or another previously applied layer of the free-radically crosslinked build material;
III) repeating step II) until the precursor is formed;
wherein the depositing of the free-radically crosslinked build material at least in step II) comprises exposing and/or irradiating a selected region of a free-radically crosslinkable build material corresponding to the respectively selected cross section of the precursor;
wherein the carrier is disposed within a container providing the free-radically crosslinkable build material, wherein the carrier is vertically raisable counter to the direction of gravity and wherein the carrier is additionally raised by a predetermined distance prior to each step II), such that a layer of the free-radically crosslinkable build material forms below a lowermost layer of the build material as viewed in a vertical direction;
wherein the free-radically crosslinkable build material comprises a thermoplastic free-radically crosslinkable polyurethane having a urethane group content of ≥15% by weight to ≤30% by weight and a photoinitiator; and
wherein the free-radically crosslinkable build material comprises an isocyanate trimerization catalyst;
wherein the free-radically crosslinkable build material is heated in step II) to a processing temperature greater than a melting point, determined by dynamic differential calorimetry, first heating, at a heating rate of 20 K/min, of the free-radically crosslinkable polyurethane;
wherein the free-radically crosslinkable polyurethane has a melting point, determined by dynamic differential calorimetry, first heating, at a heating rate of 20 K/min, of ≥50° C.; and
wherein, after step III), the article is formed by allowing the precursor to cool to a temperature of about 20° C., or wherein, after step III), the article is formed by performing step IV):
IV) performing a chemical reaction in the precursor obtained after step III) to obtain the article.
2 . The method as claimed in claim 1 , wherein the free-radically crosslinkable build material comprises further functional groups in blocked or unblocked form other than free-radically crosslinkable functional groups that are reactive towards functional groups other than free-radically crosslinkable functional groups for increasing mechanical strength in the build material.
3 . The method as claimed in claim 2 , wherein the free-radically crosslinkable build material comprises a polyamine component.
4 . The method as claimed in claim 2 , wherein the free-radically crosslinkable build material comprises blocked or unblocked NCO groups.
5 . The method as claimed in claim 4 , wherein the free-radically crosslinkable build material comprises groups having Zerewitinoff-active hydrogen atoms and one or more cyclic tin compounds of the formula F-I, F-II, F-III, or a combination thereof:
wherein:
D is —O—, —S— or —N(R1)—
where R1 is a saturated or unsaturated, linear or branched, aliphatic or cycloaliphatic radical or an optionally substituted aromatic or araliphatic radical which has up to 20 carbon atoms and optionally comprises heteroatoms from the group of oxygen, sulfur, nitrogen, or is hydrogen or the radical
or R1 and L3 together are —Z-L5-;
D* is —O— or —S—;
X, Y and Z are identical or different radicals selected from alkylene radicals of formulae —C(R2)(R3)-, —C(R2)(R3)-C(R4)(R5)- or —C(R2)(R3)-C(R4)(R5)-C(R6)(R7)- or ortho-arylene radicals of formulae
where R2 to R11 are independently saturated or unsaturated, linear or branched, aliphatic or cycloaliphatic or optionally substituted aromatic or araliphatic radicals which have up to 20 carbon atoms and optionally comprise heteroatoms from the group of oxygen, sulfur, nitrogen, or are hydrogen;
L1, L2 and L5 are independently —O—, —S—, —OC(═O)—, —OC(═S)—, —SC(═O)—, —SC(═S)—, —OS(═O) 2 O—, —OS(═O) 2 — or —N(R12)-,
where R12 is a saturated or unsaturated, linear or branched, aliphatic or cycloaliphatic radical or an optionally substituted aromatic or araliphatic radical which has up to 20 carbon atoms and optionally comprises heteroatoms from the group of oxygen, sulfur, nitrogen, or is hydrogen;
L3 and L4 are independently —OH, —SH, —OR13, a halogen, —OC(═O)R14, —SR15, —OC(═S)R16, —OS(═O) 2 OR17, —OS(═O) 2 R18 or —NR19R20, or L3 and L4 together represent -L1-X-D-Y-L2-,
where R13 to R20 are independently saturated or unsaturated, linear or branched, aliphatic or cycloaliphatic or optionally substituted aromatic or araliphatic radicals which have up to 20 carbon atoms and optionally comprise heteroatoms from the group of oxygen, sulfur, nitrogen, or are hydrogen.
6 . The method as claimed in claim 4 , wherein the free-radically crosslinkable build material contains groups having Zerewitinoff-active hydrogen atoms and further comprising a blocking agent wherein the blocking agent is an isocyanate or the blocking agent is selected such that, after deblocking of the NCO group, no release of the blocking agent as a free molecule or as part of other molecules or molecular moieties takes place.
7 . The method as claimed in claim 1 , wherein, in step II), a multitude of energy beams simultaneously exposes and/or irradiates the selected region of the additional layer of the free-radically crosslinkable build material corresponding to the respectively selected cross section of the precursor.
8 . The method as claimed in claim 1 , wherein, in step IV), the performing of the chemical reaction includes heating to a temperature above the melting point of the free-radically crosslinkable polyurethane.
9 . The method as claimed in claim 1 , wherein the free-radically crosslinkable polyurethane at the processing temperature has a viscosity of ≤10,000 mPas based on DIN EN ISO 2884-1.
10 . The method as claimed in claim 1 , wherein the photoinitiator at the processing temperature has a half-life for its thermal degradation of ≥1 hour.
11 . The method as claimed in claim 1 , wherein the isocyanate trimerization catalyst is contained in the free-radically crosslinkable build material to increase a Martens hardness value of the free-radically crosslinked build material.