Antibacterial Toner Composition for Stable Chargeability and Image Thickness

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Solution Overview

Problem

Existing toners with antibacterial or antiviral properties often face stability issues and poor chargeability, leading to inconsistent image formation and increased thickness in electrophotographic systems.

Innovation Solution

A toner formulation with specific particle size and composition ratios of inorganic antibacterial antiviral agents, binder resin, and release agent, ensuring 1.5 ≤ X ≤ 2.5 μm for the agent diameter, 3X ≤ Y ≤ 4X for the toner base particles, and 2.8% to 5.0% by mass of the agent content, stabilizing chargeability and image formation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Object-affected harmful factors

If a material having an antibacterial or antiviral effect is added to toner, then antibacterial or antiviral function is achieved, but stable production and excellent chargeability cannot be maintained

Engineering Contradiction:
Improvebacterial or viral transmissionVSAvoidtoner production stability and chargeability
Core Design Contradiction:
Object-affected harmful factorsVSReliability

Solution Approach 1:

The patent uses an inorganic antibacterial antiviral agent as an intermediary substance that can be incorporated into the toner composition. This agent acts as a mediator between the toner base and the antibacterial antiviral function requirement, allowing the toner to gain protective properties while maintaining its electrostatic and developing characteristics through proper composition design

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The patent applies parameter changes by precisely controlling the particle size of the inorganic antibacterial antiviral agent (1.5-2.5 μm number average diameter) and its content in the toner (2.8-5.0% by mass). These parameter optimizations ensure that the antibacterial antiviral function is achieved while maintaining stable production and excellent chargeability of the toner

Inventive Principle:
Principle #35Parameter changes

2Object-affected harmful factors

If conventional toner composition is used, then good chargeability is achieved, but image thickness becomes excessively large when antibacterial antiviral materials are added

Engineering Contradiction:
Improvebacterial or viral transmissionVSAvoidimage layer thickness
Core Design Contradiction:
Object-affected harmful factorsVSLength of moving object

Solution Approach 1:

The patent optimizes the particle size parameter of the inorganic antibacterial antiviral agent to a number average diameter of 1.5-2.5 μm, which is carefully selected to balance antibacterial efficacy with minimal impact on image thickness. This parameter control prevents excessive layer buildup while ensuring sufficient antibacterial protection

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent applies local quality by concentrating the antibacterial antiviral function in specifically sized inorganic particles distributed within the toner composition. This localized functional design ensures that the antibacterial effect is achieved without requiring a uniformly thick layer, thus controlling overall image thickness

Inventive Principle:
Principle #3Local quality

3Object-affected harmful factors

If inorganic antibacterial antiviral agent particles are added to toner, then antibacterial or antiviral effect is achieved, but toner production stability deteriorates

Engineering Contradiction:
Improvebacterial or viral transmissionVSAvoidtoner production stability
Core Design Contradiction:
Object-affected harmful factorsVSEase of manufacture

Solution Approach 1:

The patent specifies precise parameter ranges for the inorganic antibacterial antiviral agent, including particle size (number average diameter 1.5-2.5 μm) and content (2.8-5.0% by mass). These controlled parameters ensure that the antibacterial antiviral particles can be consistently incorporated into the toner without causing production instability

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent uses inorganic antibacterial antiviral agents with specific local properties (particle size, shape, and composition) that are optimized for both functionality and manufacturability. This localized optimization of particle characteristics enables stable production while maintaining antibacterial antiviral efficacy

Inventive Principle:
Principle #3Local quality

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

Stable and effective antibacterial or antiviral image formation with excellent chargeability, maintaining image thickness and preventing device damage, while ensuring sustained antibacterial or antiviral efficacy.

Implementation Method 1

a latent image formed by electrostatic charge is formed on a photoconductor formed of a photoconductive material, a charged toner is deposited on the latent image

Methodology Applied
Scientific EffectElectrostatic charge: Electrostatics

Implementation Method 2

a charged toner is deposited on the latent image to form a visible image

Methodology Applied
Scientific EffectElectrostatic deposition: Electrostatic Deposition

Data Source

PatentUS12607949B2Image forming method, toner, developer, printed product, toner storage unit, and image forming apparatus
Publication Date: 2026.04.21 RICOH CO LTD
  • US12607949B2 patent drawing
  • US12607949B2 patent drawing
  • US12607949B2 patent drawing

AI summary

An image forming method includes forming an electrostatic latent image on an electrostatic latent image bearer, developing the electrostatic image with a toner to form a visible image, transferring the visible image onto a recording medium, and fixing the transferred visible image on the recording medium. The toner includes toner base particles each including a binder resin, a release agent, and particles of an inorganic antibacterial antiviral agent, and satisfies conditions (1) to (3) below. The image forming method satisfies a relationship of 2.0X (micrometers)≤Z≤2.5X (micrometers). Conditions (1) the number average particle diameter X of the particles of the inorganic antibacterial antiviral agent is 1.5 (micrometers)≤X≤2.5 (micrometers), (2) 3X (micrometers)≤Y≤4X (micrometers), and (3) an amount of the inorganic antibacterial antiviral agent in the toner is 2.8% by mass or greater, but 5.0% by mass or less.