Sterilization Chamber Nozzle Integration for Vapor Distribution

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Solution Overview

Problem

Existing container sterilization devices face challenges in creating a vapor-enriched atmosphere due to large sterilization chambers, leading to inefficient disinfection and time-consuming nozzle adjustments, with permanent wetting and incorrect positioning issues.

Innovation Solution

A device with a compact sterilization chamber and integrated application devices within the chamber walls, using nozzles to apply sterilization medium directly to containers, reducing unnecessary tubing and allowing for efficient vapor distribution, along with a discharge system for gas extraction and supply of sterile air to maintain a controlled atmosphere.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Volume of moving object

If a large sterilisation chamber is used to transport containers, then container transport capacity is improved, but vapor distribution efficiency deteriorates

Engineering Contradiction:
Improvesterilisation chamber volumeVSAvoidvapor distribution efficiency
Core Design Contradiction:
Volume of moving objectVSProductivity

Solution Approach 1:

The sterilisation chamber is segmented into multiple zones with individually controllable nozzles. Each zone can be independently activated to create localized vapor enrichment, allowing efficient sterilisation even in large chambers. The chamber volume is effectively divided into smaller functional segments that can be treated separately.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

Different regions of the sterilisation chamber are equipped with nozzles having different spray characteristics and vapor generation capabilities. The vapor distribution is optimized locally in each region rather than using a uniform approach throughout the entire large chamber, ensuring efficient vapor enrichment in all areas.

Inventive Principle:
Principle #3Local quality

2Ease of operation

If individually arranged nozzles mounted in tubes are used, then targeted spraying is improved, but adjustment time and positioning accuracy deteriorate

Engineering Contradiction:
Improvetargeted spraying capabilityVSAvoidnozzle adjustment time
Core Design Contradiction:
Ease of operationVSLoss of time

Solution Approach 1:

The nozzles are pre-positioned and pre-adjusted during manufacturing to optimal angles and positions for targeted spraying. This preliminary configuration eliminates the need for time-consuming on-site adjustments, while still maintaining the ability to deliver sterilisation medium precisely to container surfaces.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The nozzle system is designed to automatically adjust or maintain optimal positioning through self-aligning mechanisms or fixed mounting structures that inherently provide correct orientation. This eliminates manual intervention and reduces adjustment time while preserving targeted spraying capability.

Inventive Principle:
Principle #25Self-service

3Ease of manufacture

If tubes are laid within the sterilisation chamber to transport sterilisation medium, then medium delivery is improved, but device complexity and cleaning difficulty increase

Engineering Contradiction:
Improvesterilisation medium deliveryVSAvoidtubing arrangement complexity
Core Design Contradiction:
Ease of manufactureVSDevice complexity

Solution Approach 1:

The complex tubing system is extracted from the interior of the sterilisation chamber and relocated to the exterior. Only essential nozzle components remain inside, dramatically simplifying the internal chamber structure and making cleaning and maintenance much easier while preserving the ability to deliver sterilisation medium to all required locations.

Inventive Principle:
Principle #2Taking out (Extraction)

4Reliability

If permanent wetting of containers is attempted, then sterilisation coverage is improved, but operational flexibility and drying efficiency deteriorate

Engineering Contradiction:
Improvesterilisation coverageVSAvoidoperational flexibility
Core Design Contradiction:
ReliabilityVSAdaptability or versatility

Solution Approach 1:

The sterilisation medium application is implemented as a periodic or pulsed process rather than continuous wetting. Containers receive controlled bursts of sterilisation medium that provide sufficient coverage, followed by drying phases. This periodic approach maintains reliable sterilisation while allowing operational flexibility and preventing excessive moisture accumulation.

Inventive Principle:
Principle #19Periodic action

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

This design enables efficient and targeted sterilization with reduced chamber volume, ensuring consistent exposure to disinfectants, minimizing gas entry and exit, and facilitating faster machine access while maintaining a controlled environment for effective disinfection.

Implementation Method 1

The application device comprises one or more nozzles which apply the sterilisation medium to the containers

Methodology Applied
Scientific EffectSpray: Spray

Implementation Method 2

the device has a discharge device for discharging a gaseous medium from the sterilisation chamber

Methodology Applied
Scientific EffectGas extraction:

Data Source

PatentUS8652414B2Device for sterilising containers
Publication Date: 2014.02.18 KRONES AG
  • US8652414B2 patent drawing
  • US8652414B2 patent drawing
  • US8652414B2 patent drawing

AI summary

A device for treating containers, with a housing, a sterilization chamber formed within the housing to sterilize the containers, with a transport device which transports the containers along a pre-specified transport path (P) through the sterilization chamber, and with at least one application device which applies a liquid sterilization medium to the containers during their transport through the sterilization chamber. The application device is integrated at least partly in a wall of the sterilization chamber.