Fluid Sterilization System Using Dynamic Thermal Profiles

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Solution Overview

Problem

Current fluid sterilization methods, such as reverse osmosis, membrane technology, UV light, and high-temperature heating, are energy-intensive, require frequent maintenance, and are ineffective against prions, leading to costly disposal of medical equipment and limited accessibility to clean water, especially in developing regions.

Innovation Solution

A system that uses a heating section to sterilize pressurized fluid by maintaining prescribed temperature and pressure profiles, utilizing a heat exchanger for preheating and cooling, and operating valves in a controlled sequence to achieve sterilization without fixed temperature or pressure within the system, allowing for continuous flow and potential recirculation or autoclave chamber use.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If high-temperature heating is used to sterilize fluid, then sterilization effectiveness is improved, but energy consumption and equipment size increase

Engineering Contradiction:
Improvesterilization effectivenessVSAvoidenergy consumption
Core Design Contradiction:
ReliabilityVSUse of energy by moving object

Solution Approach 1:

The system dynamically adjusts temperature and pressure parameters during the sterilization process. By varying these parameters over time rather than maintaining constant high values, the system achieves effective sterilization while reducing overall energy consumption and equipment size requirements.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The sterilization process employs periodic heating and cooling cycles. The fluid is heated to sterilization temperatures, then cooled down, creating a periodic action that reduces the total energy input required compared to continuous high-temperature maintenance, while still achieving effective sterilization.

Inventive Principle:
Principle #19Periodic action

2Reliability

If high-temperature heating is used to sterilize fluid, then sterilization effectiveness is improved, but apparatus size increases

Engineering Contradiction:
Improvesterilization effectivenessVSAvoidapparatus size
Core Design Contradiction:
ReliabilityVSVolume of stationary object

Solution Approach 1:

By changing temperature and pressure parameters dynamically rather than maintaining constant high values, the system achieves effective sterilization in a more compact apparatus. The parameter variation allows for smaller heat-sink apparatus compared to traditional high-temperature continuous systems.

Inventive Principle:
Principle #35Parameter changes

3Reliability

If reverse osmosis or membrane technology is used for sterilization, then fluid purification is achieved, but maintenance requirements and operational costs increase

Engineering Contradiction:
Improvefluid purificationVSAvoidmaintenance requirements
Core Design Contradiction:
ReliabilityVSEase of repair

Solution Approach 1:

The system replaces mechanical filtration systems (reverse osmosis, membranes) with a thermal field-based sterilization approach. By using controlled heating and cooling cycles rather than physical barriers, the system eliminates the need for membrane replacement and complex mechanical maintenance while achieving effective fluid purification.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

4Reliability

If UV light technology is used for sterilization, then fluid sterilization is achieved, but operational costs and maintenance increase

Engineering Contradiction:
Improvefluid sterilizationVSAvoidmaintenance costs
Core Design Contradiction:
ReliabilityVSEase of repair

Solution Approach 1:

The system replaces UV light sterilization with a thermal field approach using controlled heating and cooling. This substitution eliminates the need for UV bulbs that require frequent replacement and maintenance, reducing operational costs while maintaining effective fluid sterilization capability.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

5Reliability

If prion sterilization is attempted with current methods, then treatment is applied, but effectiveness is insufficient leading to equipment disposal

Engineering Contradiction:
Improveprion inactivationVSAvoidequipment disposal
Core Design Contradiction:
ReliabilityVSLoss of substance

Solution Approach 1:

The system employs extreme parameter changes including high temperature and pressure variations that are specifically effective against prions. These intensified parameter changes enable the inactivation of prions on medical equipment, eliminating the need for disposal and reducing healthcare costs.

Inventive Principle:
Principle #35Parameter changes

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

The system effectively sterilizes fluids and equipment by maintaining precise temperature and pressure conditions, reducing energy consumption and maintenance needs, and effectively inactivating prions, making it suitable for various applications, including medical and water purification.

Implementation Method 1

a heating section to heat pressurized fluid above prescribed thresholds for temperature, pressure, and duration

Methodology Applied
Scientific EffectHeating: Heating

Implementation Method 2

a heat exchanger to both (a) preheat fluid prior to entering the heating section

Methodology Applied
Scientific EffectHeat transfer: Heat Exchanger

Implementation Method 3

a heat exchanger to both (a) preheat fluid prior to entering the heating section and (b) cool outflow of the heating apparatus

Methodology Applied
Scientific EffectCooling: Cooling

Data Source

PatentUS10213517B2System for fluid sterilization
Publication Date: 2019.02.26 PAPADOPOULOS MICHAEL
  • US10213517B2 patent drawing
  • US10213517B2 patent drawing
  • US10213517B2 patent drawing

AI summary

A system of fluid sterilization is provided, which incorporates a heating section to heat pressurized fluid above prescribed thresholds for temperature, pressure, and duration (e.g., dwell time) to achieve desired levels of sterilization, including a heat exchanger to both (a) preheat fluid prior to entering the heating section and (b) cool outflow of the heating apparatus, in which fluid travels through the apparatus by operating valves forward and aft of the heating section in a controlled sequence to facilitate flow through the system while maintaining prescribed pressure and temperature profiles. The system operates within prescribed ranges of pressure and temperature to achieve the desired level of sterilization without need of maintaining a fixed temperature or a fixed pressure within any portion of the system, including the heating section.