Method for preparing biomass-based conductive hydrogel by 3D printing

Abstract

A method for preparing a biomass-based conductive hydrogel by 3D printing is provided. Firstly, a cellulose-based macromonomer, a rosin-based monomer, an acrylic acid monomer and an initiator are mixed in a certain proportion, stirred, and dissolved at 25-70° C. Then, diisocyanate in an amount of 5-10 wt % of a total mass of the monomers is added to the mixed solution and mixed uniformly to prepare a 3D printing photosensitive resin solution. An SLA light-curing 3D printer is used to print a hydrogel precursor 1 with a complex shape. Next, the hydrogel precursor 1 is heated to obtain a hydrogel precursor 2 with a dual-curing network. Finally, the obtained hydrogel precursor 2 is swelled in a 1-15 wt % alkaline solution at 5-60° C. for 0.1-10 hours to obtain the biomass-based conductive hydrogel.

Claims

1. A method for preparing a biomass-based conductive hydrogel by 3D printing, comprising the following steps: step 1: mixing an ethyl cellulose-based macromonomer, a rosin-based monomer, an acrylic acid monomer and an initiator in a certain proportion, stirring and dissolving at 25-70° C.; and then, adding diisocyanate in an amount of 5-10 wt % of a total mass of the monomers to the mixed solution and mixing uniformly to prepare a 3D printing photosensitive resin solution, wherein the ethyl cellulose-based macromonomer described in step 1 has the following structure: ##STR00003## wherein the ethyl cellulose used therein has a viscosity of any one of 3-7 mPa.Math.s, 9-11 mPa.Math.s, 18-22 mPa.Math.s, 45-55 mPa.Math.s, 90-110 mPa.Math.s, 180-220 mPa.Math.s and 270-330 mPa.Math.s, and R is hydrogen or ethyl group, wherein the rosin-based monomer described in step 1 has the following structure: ##STR00004## wherein R denotes a rosin structure, and the used rosin is any one of L-pimaric acid, abietic acid, dehydroabietic acid, pimaric acid and disproportionated rosin, wherein the acrylic acid monomer described in step 1 is one of hydroxyethyl acrylate, hydroxyethyl methacrylate and hydroxypropyl acrylate; step 2: using an SLA light-curing 3D printer to print a hydrogel precursor 1 with a complex shape, and then heating the hydrogel precursor 1 to obtain a hydrogel precursor 2 with a dual-curing network, wherein the heat treatment described in step 2 is performed at 70-150° C. for 4-10 hours; and step 3: finally, swelling the obtained hydrogel precursor 2 in a 1-15 wt % alkaline solution at 5-60° C. for 0.1-10 hours to obtain the biomass-based conductive hydrogel.

2. The method for preparing the biomass-based conductive hydrogel by 3D printing according to claim 1, wherein the initiator described in step 1 is one of (2,4,6-trimethylbenzoyl)diphenylphosphine oxide, benzil dimethyl ketal and 2-hydroxy-4′-(2-hydroxyethoxy)-2-methylpropiophenone.

3. The method for preparing the biomass-based conductive hydrogel by 3D printing according to claim 1, wherein the diisocyanate described in step 1 is one of toluene diisocyanate (TDI), isophorone diisocyanate (IPDI), methylenediphenyl diisocyanate (MDI), dicyclohexylmethane diisocyanate (HMDI), hexamethylene diisocyanate (HDI) and lysine diisocyanate (LDI).

4. The method for preparing the biomass-based conductive hydrogel by 3D printing according to claim 1, wherein the certain proportion described in step 1 is a mass ratio of [the ethyl cellulose-based macromonomer]: [the rosin-based monomer]: [the acrylic acid monomer]: [the initiator]=[0.2-1]: [1-5]: [5-9]: [0.1-0.5].

5. The method for preparing the biomass-based conductive hydrogel by 3D printing according to claim 1, wherein the alkaline solution described in step 3 is one of a sodium hydroxide solution and a potassium hydroxide solution.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 shows pictures of a hydrogel precursor 2 before and after swelling in Example 1;

(2) FIG. 2 shows pictures of bending and conductivity tests on the hydrogel precursor 2 after swelling in Example 1; and

(3) FIG. 3 shows a stress-strain curve of the hydrogel precursor 2 after swelling in Example 1.

DESCRIPTION OF THE EMBODIMENTS

(4) Because a method for preparing a biomass-based conductive hydrogel by 3D printing has a great impact, the content of the present invention is further described below with reference to specific examples. However, these examples are not intended to limit the protection scope of the present invention.

(5) Example 1: preparation of a biomass-based conductive hydrogel in a ratio of [an ethyl cellulose-based macromonomer]: [a rosin-based monomer]: [an acrylic acid monomer]: [an initiator]=0.3:2:8:0.2.

(6) Step 1: First, 0.9 g of ethyl cellulose-based macromonomer with a viscosity of 3-7 mPa.Math.s, 6 g of disproportionated rosin-based monomer, 24 g of hydroxyethyl acrylate, and 0.6 g of (2,4,6-trimethylbenzoyl)diphenylphosphine oxide were mixed, and stirred and sufficiently dissolved at 70° C.; and then 1.5 g of hexamethylene diisocyanate was added to the mixed solution and mixed uniformly to prepare a 3D printing photosensitive resin solution.

(7) Step 2: An SLA light-curing 3D printer was used to print a hydrogel precursor 1 with a complex shape, and then the hydrogel precursor 1 was heated at 110° C. for 8 hours to obtain a hydrogel precursor 2 with a dual-curing network.

(8) Step 3: Finally, the obtained hydrogel precursor 2 was swelled in a 10 wt % sodium hydroxide solution at 40° C. for 5 hours to obtain the biomass-based conductive hydrogel.

(9) Example 2: preparation of a biomass-based conductive hydrogel in a ratio of [an ethyl cellulose-based macromonomer]: [a rosin-based monomer]: [an acrylic acid monomer]: [an initiator]=0.3:2:8:0.2.

(10) Step 1 was identical to that in Example 1.

(11) Step 2: An SLA light-curing 3D printer was used to print a hydrogel precursor 1 with a complex shape, and then the hydrogel precursor 1 was heated at 80° C. for 5 hours to obtain a hydrogel precursor 2 with a dual-curing network.

(12) Step 3: Finally, the obtained hydrogel precursor 2 was swelled in a 5 wt % potassium hydroxide solution at 20° C. for 4 hours to obtain the biomass-based conductive hydrogel.

(13) Example 3: preparation of a biomass-based conductive hydrogel in a ratio of [an ethyl cellulose-based macromonomer]: [a rosin-based monomer]: [an acrylic acid monomer]: [an initiator]=0.5:4:6:0.3.

(14) Step 1: First, 1 g of ethyl cellulose-based macromonomer with a viscosity of 90-110 mPa.Math.s, 8 g of dehydroabietic acid monomer, 12 g of hydroxyethyl acrylate, and 0.6 g of benzil dimethyl ketal were mixed, and stirred and sufficiently dissolved at 60° C.; and then 1.6 g of toluene diisocyanate was added to the mixed solution and mixed uniformly to prepare a 3D printing photosensitive resin solution.

(15) Step 2 was identical to that in Example 1.

(16) Step 3 was identical to that in Example 1.

(17) Example 4: preparation of a biomass-based conductive hydrogel in a ratio of [an ethyl cellulose-based macromonomer]: [a rosin-based monomer]: [an acrylic acid monomer]: [an initiator]=0.5:4:6:0.3.

(18) Step 1 was identical to that in Example 3.

(19) Step 2: An SLA light-curing 3D printer was used to print a hydrogel precursor 1 with a complex shape, and then the hydrogel precursor 1 was heated at 80° C. for 5 hours to obtain a hydrogel precursor 2 with a dual-curing network.

(20) Step 3: Finally, the obtained hydrogel precursor 2 was swelled in a 5 wt % potassium hydroxide solution at 20° C. for 4 hours to obtain the biomass-based conductive hydrogel.

(21) Example 5: preparation of a biomass-based conductive hydrogel in a ratio of [an ethyl cellulose-based macromonomer]: [a rosin-based monomer]: [an acrylic acid monomer]: [an initiator]=0.5:4:6:0.3.

(22) Step 1: First, 1 g of ethyl cellulose-based macromonomer with a viscosity of 270-330 mPa.Math.s, 8 g of dehydroabietic acid monomer, 12 g of hydroxyethyl acrylate, and 0.6 g of (2,4,6-trimethylbenzoyl)diphenylphosphine oxide were mixed, and stirred and sufficiently dissolved at 60° C.; and then 2 g of toluene diisocyanate was added to the mixed solution and mixed uniformly to prepare a 3D printing photosensitive resin solution.

(23) Step 2: An SLA light-curing 3D printer was used to print a hydrogel precursor 1 with a complex shape, and then the hydrogel precursor 1 was heated at 100° C. for 8 hours to obtain a hydrogel precursor 2 with a dual-curing network.

(24) Step 3: Finally, the obtained hydrogel precursor 2 was swelled in a 10 wt % sodium hydroxide solution at 50° C. for 5 hours to obtain the biomass-based conductive hydrogel.

(25) Example 6: preparation of a biomass-based conductive hydrogel in a ratio of [an ethyl cellulose-based macromonomer]: [a rosin-based monomer]: [an acrylic acid monomer]: [an initiator]=0.3:2:8:0.2.

(26) Step 1: First, 0.9 g of ethyl cellulose-based macromonomer with a viscosity of 3-7 mPa.Math.s, 6 g of disproportionated rosin-based monomer, 24 g of hydroxyethyl methacrylate, and 0.6 g of 2-hydroxy-4′-(2-hydroxyethoxy)-2-methylpropiophenone were mixed, and stirred and sufficiently dissolved at 70° C.; and then 1.5 g of hexamethylene diisocyanate was added to the mixed solution and mixed uniformly to prepare a 3D printing photosensitive resin solution.

(27) Step 2: An SLA light-curing 3D printer was used to print a hydrogel precursor 1 with a complex shape, and then the hydrogel precursor 1 was heated at 110° C. for 5 hours to obtain a hydrogel precursor 2 with a dual-curing network.

(28) Step 3: Finally, the obtained hydrogel precursor 2 was swelled in a 5 wt % sodium hydroxide solution at 40° C. for 8 hours to obtain the biomass-based conductive hydrogel.

(29) Analysis of Spectra

(30) FIG. 1 shows pictures of the hydrogel precursor 2 before and after swelling in Example 1. It can be found from the figure that the hydrogel obtained after swelling significantly increases in volume, but still maintains a 3D shape. It is shown that the hydrogel obtained after swelling has excellent shape fidelity, which further indicates that the preparation method of the present invention can prepare a hydrogel with a complex shape.

(31) FIG. 2 shows pictures of bending and conductivity tests on the hydrogel precursor 2 after swelling in Example 1. It can be found from the figure that the hydrogel obtained after swelling has excellent flexibility and can be bent in any way; and exhibits excellent conductivity and can light up the bulb when being connected to a circuit.

(32) FIG. 3 shows a stress-strain curve of the hydrogel precursor 2 after swelling in Example 1. It can be found from the figure that the hydrogel obtained after swelling exhibits excellent mechanical properties.

(33) The foregoing examples describe the technical solution of the present invention in detail. It should be understood that, the foregoing description merely describes preferred examples of the present invention, and is not intended to limit the present invention. Any person skilled in the art can, without departing from the scope of the technical solution of the present invention, use the technical content disclosed above to make some changes or modifications into equivalent examples with equivalent changes. However, any modifications or improvements made within the principle scope of the present invention all shall fall within the scope of the present invention.