Fabrication of solid materials or films from a polymerizable liquid
The disclosure describes a polymerizable liquid that includes a reactive oligomer and a reactive monomer. The polymerizable liquid is an energy polymerizable liquid hardenable by a single reaction mechanism forming a photoplastic material. The disclosure further describes a method of producing the photoplastic material and articles that can be made from the photoplastic material.
1. A free radical polymerizable liquid, the free radical polymerizable liquid comprising:
a reactive oligomer, the reactive oligomer being at least one (i) a multi-functional methacrylate oligomer, and (ii) a multi-functional acrylate oligomer; and
a reactive monofunctional monomer, the reactive monofunctional monomer being at least one of (i) a monofunctional N-vinyl monomer, (ii) a monofunctional vinyl ether monomer, (iii) a monofunctional vinyl ester monomer, (iv) a monofunctional vinylamide monomer, (v) a styrene monomer, (vi) a monofunctional acrylamide monomer, (vii) monofunctional (meth)acrylate monomer, (viii) a cyanoacrylate monomer, (ix) a monofunctional vinyl carbonate monomer, (x) a monofunctional acryloyl monomer, and (xi) a monofunctional vinyl carbamate monomer,
wherein a molar bond ratio of the reactive ethylenically unsaturated groups of the reactive monofunctional species to the reactive ethylenically unsaturated groups of the reactive multi-functional species is at least 10:1,
wherein a total weight % of the reactive monofunctional species in the calculation of the molar bond ratio is at least 25% of the polymerizable liquid, and
wherein a total weight % of the reactive multifunctional species in the calculation of the molar bond ratio is at least 25% of the polymerizable liquid,
the free radical polymerizable liquid being an energy polymerizable liquid hardenable by a single reaction mechanism forming a photoplastic material.
2. The polymerizable liquid of claim 1 , further comprising a photoinitiator from about 0.01 percent to about 15 percent by weight.
3. The polymerizable liquid of claim 1 , wherein the polymerizable liquid has a toughness equal to or greater than a utilization curve defined by the expressions: 1) ultimate tensile strength (MPa) =−0.75 X elongation +130 for elongations from about 15% to about 95%, 2) ultimate tensile strength (MPa) =4500/(elongation −25) 5 for elongations from about 95% to about 500%.
4. The polymerizable liquid of claim 1 , wherein the polymerizable liquid has a toughness equal to or greater than a utilization curve defined by the expressions: 1) ultimate tensile strength (MPa) =−1 X elongation +120 for elongations from less than 95%, 2) ultimate tensile strength (MPa) =3000/(elongation +10) −3 for elongations from about 95% to about 850% 3) ultimate tensile strength (MPa) =0.5 for elongations greater than about 850%.
5. The polymerizable liquid of claim 1 , wherein the polymerized material reaches prescribed mechanical properties without supplied heat.
6. The polymerizable liquid of claim 1 , further comprising at least one of a non-reactive light absorbing pigment in an amount from about 0.001 percent to about 10 percent by weight, a filler, a polymerization inhibitor, and a polymerization catalyst.
7. The polymerizable liquid of claim 1 , further comprising a non-reactive light absorbing pigment in an amount from about 0.001 percent to about 10 percent by weight, and a filler.
8. The polymerizable liquid of claim 1 , wherein the reactive oligomer and the reactive monofunctional monomer react by a same polymerization mechanism and have different reaction rates.
9. The polymerizable liquid of claim 1 , wherein the solubility of the reactive monofunctional monomer and the reactive oligomer change during polymerization, which assists homopolymerization of either the monomeric or oligomeric species.
10. The polymerizable liquid of claim 1 , wherein polymerization creates a material with more than one glass transition temperature.
11. The polymerizable liquid of claim 1 , wherein polymerization creates a material with two different glass transition temperatures, with a difference in Tg by at least 60 degrees C.
12. The polymerizable liquid of claim 1 , wherein the molar bond ratio of the reactive ethylenically unsaturated groups of the reactive monofunctional species to the reactive ethylenically unsaturated groups of the reactive multi-functional species is at least 20:1.
13. The polymerizable liquid of claim 12 , wherein the molar bond ratio of the reactive ethylenically unsaturated groups of the reactive monofunctional species to the reactive ethylenically unsaturated groups of the reactive multi-functional species is at least 30:1.
14. The polymerizable liquid of claim 1 , wherein the polymerizable liquid forms a print on a substrate.
15. The polymerizable liquid of claim 1 , wherein the polymerizable liquid is hardened to form a film or three-dimensional object by stereolithography (SLA), digital light projection (DLP), material jetting, or inkjet printing.
16. The polymerizable liquid of claim 15 , wherein the thickness of the inkjet film or the 3D printed layer is greater than about 30 um.
17. The polymerizable liquid of claim 1 , wherein when hardened the polymerizable liquid has adjustable mechanical properties resulting from changing the energy polymerization conditions.
18. The polymerizable liquid of claim 1 , wherein the polymerizable liquid is non-toxic.
19. The polymerizable liquid of claim 1 , wherein the reactive oligomer has a molecular weight greater than about 1500 grams / mole.
20. The polymerizable liquid of claim 19 , wherein the reactive oligomer has a molecular weight greater than about 4000 grams / mole.
21. The polymerizable liquid of claim 1 , wherein the reactive monofunctional monomer is a mono-functional N-vinyl, vinyl ester, or acryloyl selected from the group consisting of N-Vinylpyrrolidone, N-Vinylcaprolactam, N-Vinylformamide, Acryloyl morpholine or Vinyl cinnamate.