Split Flow Tube for Selective Ionization in Mass Spectrometry

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Solution Overview

Problem

Current analytical techniques for detecting threat agents and illicit substances at ultra-low levels face challenges in sensitivity and selectivity, requiring multiple sampling events and instruments due to limited ionization mechanisms, which increases chemical noise and complicates detection of multiple analytes simultaneously.

Innovation Solution

A split flow tube system with multiple ionization sources, including corona discharge sources, is used to facilitate selective ionization and analysis of analytes, allowing for simultaneous detection of multiple substances in a single sampling event by separating reaction regions and controlling reactant ion chemistry with suction and varying air flow rates.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Adaptability or versatility

If multiple sampling events and instruments are used to detect various threat agents and illicit substances, then detection coverage is improved, but system complexity and time consumption increase

Engineering Contradiction:
Improvedetection coverageVSAvoidsystem complexity
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The patent implements a single analytical system capable of performing multiple detection functions by integrating different ionization sources (electron impact, chemical ionization, atmospheric pressure chemical ionization) and multiple reaction chambers within one mass spectrometer platform. This allows the system to detect various threat agents and illicit substances with different chemical properties using a single instrument rather than requiring multiple specialized instruments, thereby reducing system complexity while maintaining broad detection coverage

Inventive Principle:
Principle #6Universality (Multi-functionality)

Solution Approach 2:

The patent divides the analytical system into multiple independent reaction chambers, each optimized for specific types of analytes or ionization mechanisms. This segmentation allows simultaneous or sequential analysis of different substance classes within a single sampling event, improving versatility without requiring multiple complete instrument systems

Inventive Principle:
Principle #1Segmentation

2Measurement precision

If sensitivity is increased without improving selectivity, then detection limit is improved, but chemical noise increases

Engineering Contradiction:
Improvedetection limitVSAvoidchemical noise
Core Design Contradiction:
Measurement precisionVSObject-generated harmful factors

Solution Approach 1:

The patent employs different ionization sources and reaction chamber configurations optimized for specific analyte types. For example, electron impact ionization with specific electron energies is used for certain explosives, while chemical ionization is used for other substance classes. This localized optimization of ionization conditions for specific analyte groups improves selectivity, allowing enhanced sensitivity without proportional increases in chemical noise from non-target compounds

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The patent uses selected reactant ions as intermediaries in chemical ionization reactions to achieve selective analyte detection. By controlling the type and energy of reactant ions introduced into reaction chambers, the system can selectively ionize target analytes while leaving interfering substances unaffected, thereby improving signal-to-noise ratio and enabling lower detection limits without increased chemical noise

Inventive Principle:
Principle #24Intermediary (Mediator)

3Device complexity

If a single ionization source is used, then device complexity is reduced, but ability to detect multiple analyte types is limited

Engineering Contradiction:
Improveinstrument configurationVSAvoidanalyte detection capability
Core Design Contradiction:
Device complexityVSAdaptability or versatility

Solution Approach 1:

The patent integrates multiple ionization sources (electron impact, chemical ionization, atmospheric pressure chemical ionization) within a single mass spectrometer system, allowing the instrument to adapt to different analyte types through software control and source selection rather than requiring physically separate instruments. This multi-functional approach maintains relatively simple device architecture while significantly expanding analyte detection capability across diverse chemical classes

Inventive Principle:
Principle #6Universality (Multi-functionality)

Solution Approach 2:

The patent implements dynamic switching between different ionization modes and reaction chamber configurations based on the analyte being detected. The system can change ionization source activation, reactant ion types, and chamber conditions in real-time during analysis, providing adaptability to detect multiple analyte types without requiring a permanently complex multi-instrument setup

Inventive Principle:
Principle #15Dynamics

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 enhances sensitivity and selectivity, enabling the detection of analytes at parts-per-trillion levels without the need for multiple sampling events, improving the ability to analyze multiple substances concurrently with a single system.

Implementation Method 1

A split flow tube system with multiple ionization sources, including corona discharge sources, is used to facilitate selective ionization and analysis of analytes

Methodology Applied
Scientific EffectCorona discharge: Corona Discharge

Data Source

PatentUS11043370B2Device and system for selective ionization and analyte detection and method of using the same
Publication Date: 2021.06.22 BATTELLE MEMORIAL INST
  • US11043370B2 patent drawing
  • US11043370B2 patent drawing
  • US11043370B2 patent drawing

AI summary

Disclosed herein are embodiments of a system for selectively ionizing samples that may comprise a plurality of different analytes that are not normally detectable using the same ionization technique. The disclosed system comprises a unique split flow tube that can be coupled with a plurality of ionization sources to facilitate using different ionization techniques for the same sample. Also disclosed herein are embodiments of a method for determining the presence of analytes in a sample, wherein the number and type of detectable analytes that can be identified is increased and sensitivity and selectivity are not sacrificed.