C09D11/037

Paste manufacturing method and flexible electrode manufacturing method using the same

A method of manufacturing a paste according to various embodiments of the present disclosure for resolving the above-described problems is disclosed. The method of manufacturing a paste may include an operation of adding a metal conductor and a multi-walled carbon nanotube (MWCNT) to chloroform (CHCl.sub.3) to produce a first mixture, an operation of adding polydimethylsiloxane (PDMS) to the first mixture to produce a second mixture, an operation of evaporating the chloroform in the second mixture to acquire a third mixture, and an operation of adding an additional additive to the third mixture to produce a paste.

WATER-BASED INK FOR INK-JET RECORDING
20210340395 · 2021-11-04 · ·

A water-based ink for ink-jet recording includes: a solid solution of a quinacridone pigment including C.I. Pigment Red 202 and C.I. Pigment Violet 19; an azo pigment including C.I. Pigment Red 146; and water. A mass ratio (Q:A) of a content amount (Q) of the solid solution of the quinacridone pigment to a content amount (A) of the azo pigment in an entire amount of the water-based ink is in a range of 9:1 to 2:8.

WATER-BASED INK FOR INK-JET RECORDING
20210340395 · 2021-11-04 · ·

A water-based ink for ink-jet recording includes: a solid solution of a quinacridone pigment including C.I. Pigment Red 202 and C.I. Pigment Violet 19; an azo pigment including C.I. Pigment Red 146; and water. A mass ratio (Q:A) of a content amount (Q) of the solid solution of the quinacridone pigment to a content amount (A) of the azo pigment in an entire amount of the water-based ink is in a range of 9:1 to 2:8.

PHOTO-CURABLE ELASTIC INK COMPOSITION FOR THREE-DIMENSIONAL PRINTING
20210340393 · 2021-11-04 ·

The present disclosure provides a photo-curable elastic ink composition for three-dimensional printing and the preparation method. The ink composition includes approximately 10%-75% of a soft monomer, approximately 10%-75% of a hard monomer, approximately 5%-20% of a cross-linking agent, approximately 5%-20% of a non-reactive soft resin, approximately 0.5%-10% of a photo-initiator, approximately 0%-0.5% of a colorant, and approximately 0.05%-8% of an auxiliary agent. The soft monomer is capable of generating a homopolymer with a glass transition temperature lower than about 25° C. The hard monomer is capable of generating a homopolymer with a glass transition temperature of about 25° C. or higher. The non-reactive soft resin is a resin without containing any radiation curable group in the molecular structure and having a glass transition temperature less than 0° C.

PHOTO-CURABLE ELASTIC INK COMPOSITION FOR THREE-DIMENSIONAL PRINTING
20210340393 · 2021-11-04 ·

The present disclosure provides a photo-curable elastic ink composition for three-dimensional printing and the preparation method. The ink composition includes approximately 10%-75% of a soft monomer, approximately 10%-75% of a hard monomer, approximately 5%-20% of a cross-linking agent, approximately 5%-20% of a non-reactive soft resin, approximately 0.5%-10% of a photo-initiator, approximately 0%-0.5% of a colorant, and approximately 0.05%-8% of an auxiliary agent. The soft monomer is capable of generating a homopolymer with a glass transition temperature lower than about 25° C. The hard monomer is capable of generating a homopolymer with a glass transition temperature of about 25° C. or higher. The non-reactive soft resin is a resin without containing any radiation curable group in the molecular structure and having a glass transition temperature less than 0° C.

BIOCOMPATIBLE INK
20210340390 · 2021-11-04 ·

Biocompatible ink formulations are described herein. In one example, a biocompatible ink formulation includes an ink base and a biocompatible component that, when mixed with the ink base to form the biocompatible ink formulation and subject to curing via ultraviolet light, causes the biocompatible ink formulation to be white.

BIOCOMPATIBLE INK
20210340390 · 2021-11-04 ·

Biocompatible ink formulations are described herein. In one example, a biocompatible ink formulation includes an ink base and a biocompatible component that, when mixed with the ink base to form the biocompatible ink formulation and subject to curing via ultraviolet light, causes the biocompatible ink formulation to be white.

Lithographic ink

Provided is a lithographic ink having superior surface staining resistance and fluidity. Also provided is a method for manufacturing a printed material using the lithographic ink. The lithographic ink has all of a viscosity (A) at a rotational speed of 0.5 rpm, a viscosity (B) at a rotational speed of 20 rpm, and a viscosity (C) at a rotational speed of 50 rpm of 5 Pa.Math.s or more and 100 Pa.Math.s or less, the viscosities (A), (B), and (C) being measured by using a cone-plate rotating viscometer at 25° C., and has a viscosity ratio (C)/(B) of 0.8 or more and 1.0 or less.

Lithographic ink

Provided is a lithographic ink having superior surface staining resistance and fluidity. Also provided is a method for manufacturing a printed material using the lithographic ink. The lithographic ink has all of a viscosity (A) at a rotational speed of 0.5 rpm, a viscosity (B) at a rotational speed of 20 rpm, and a viscosity (C) at a rotational speed of 50 rpm of 5 Pa.Math.s or more and 100 Pa.Math.s or less, the viscosities (A), (B), and (C) being measured by using a cone-plate rotating viscometer at 25° C., and has a viscosity ratio (C)/(B) of 0.8 or more and 1.0 or less.

Printed electronics

The present invention relates to an electronic device comprising a printed substrate comprising a trace of molecular ink thereon, the molecular ink being sintered to form a conductive metal trace forming the electronic device, wherein the molecular ink is chosen from a) a flake-less printable composition of 30-60 wt % of a C.sub.8-C.sub.12 silver carboxylate, 0.1-10 wt % of a polymeric binder and balance of at least one organic solvent, all weights based on total weight of the composition; or b) a flake-less printable composition of 5-75 wt % of bis(2-ethyl-1-hexylamine) copper (II) formate, bis(octylamine) copper (II) formate or tris(octylamine) copper (II) formate, 0.25-10 wt % of a polymeric binder and balance of at least one organic solvent, all weights based on total weight of the composition.