

ICP Time-of-Flight Mass Spectrometer
飞行时间电感耦合等离子体质谱仪
- SKU ICM-0005
- ICP-MS
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
- 21 CFR Part 11 software compliance (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Mass range | 2–260 amu |
|---|---|
| Detection limit | 1–100 ng/L typical |
| Analyzer | time of flight |
| Spectra per second | up to 1000 |
| Mass resolution | approximately 1000 |
| Collision cell | optional |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ICH Q3D Elemental Impurities, USP <233> Elemental Impurities — Procedures, USP <730> Plasma Spectrochemistry
What is the ICP Time-of-Flight Mass Spectrometer?
An ICP time-of-flight mass spectrometer records the full mass spectrum from each plasma ion pulse simultaneously. It is increasingly chosen for rapid trace multi-element analysis and especially for single-particle or single-cell biological studies.
What is the ICP Time-of-Flight Mass Spectrometer?
An ICP time-of-flight mass spectrometer records the full mass spectrum from each plasma ion pulse simultaneously. It is increasingly chosen for rapid trace multi-element analysis and especially for single-particle or single-cell biological studies.
Overview
A time-of-flight analyzer accelerates a packet of ions to the same kinetic energy and measures their arrival times at a detector, because lighter ions arrive first. This records the entire mass spectrum from a single plasma pulse, so transient signals are captured completely and no mass is missed between scans. The approach is ideal when many elements must be measured in a short interval, as in laser ablation imaging, nanoparticle analysis or single-cell inductively coupled plasma mass spectrometry. Mass resolution is moderate compared with sector instruments, and a collision or reaction cell can be added for interference control. High acquisition rates and full-spectrum collection make the technique valuable for fast transient signals that a scanning instrument would sample incompletely.
How does it work?
A plasma torch at atmospheric pressure ionizes the sample aerosol. Ions are extracted through a two-stage interface of sampling and skimmer cones into a vacuum region, then focused by ion optics and separated by a mass analyzer according to mass-to-charge ratio. The most common analyzer is a quadrupole, which scans rapidly across selected masses; sector field instruments provide high resolution or high sensitivity, multicollector instruments measure isotope ratios precisely, and time-of-flight analyzers record all masses simultaneously. Collision and reaction cells filled with helium, hydrogen or reactive gases suppress polyatomic interferences such as argon chloride on arsenic or argon argon on selenium. Detection uses electron multipliers with pulse counting and analog modes to cover a wide dynamic range. Calibration uses external standards, internal standards and, when needed, isotope dilution, with careful control of blanks and matrix effects.
What are the key features?
- Full mass spectrum from each plasma pulse
- Simultaneous detection of all masses
- Ideal for fast transient and single-particle signals
- High acquisition rate for imaging
- Optional collision reaction cell
- Moderate mass resolution compared with sectors
What are the technical specifications?
A typical icp time-of-flight mass spectrometer configuration offers mass range of 2–260 amu, detection limit of 1–100 ng/L typical, analyzer of time of flight, spectra per second of up to 1000, mass resolution of approximately 1000 and collision cell of optional. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The ICP Time-of-Flight Mass Spectrometer is used in laser ablation elemental imaging, single-particle and nanoparticle analysis, single-cell multi-element measurement and fast transient signals in chromatography. Across the wider ICP-MS class, laboratories also deploy it for elemental impurity testing per ICH Q3D and USP <233>, ultratrace metals in water and environmental samples and clinical and forensic trace element analysis.
Which standards and certifications apply?
Relevant standards and methods include ICH Q3D Elemental Impurities, USP <233> Elemental Impurities — Procedures, USP <730> Plasma Spectrochemistry, ISO 17294-2 Water quality — ICP-MS determination of elements, US EPA Method 200.8, US EPA Method 6020B and ISO/IEC 17025. Certification candidates for this model are CE, ISO 9001 manufacturing and 21 CFR Part 11 software compliance; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
ICP-MS requires high-purity argon, a vacuum system with roughing and turbomolecular pumps, stable power and a temperature-controlled room. Interface cones, torch and sample introduction parts wear and must be inspected and replaced, and cone condition affects sensitivity and stability. Contamination is critical at nanogram per litre levels, so clean sample preparation areas, ultrapure acids and dedicated labware are essential. Matrix effects require internal standards, dilution or matrix matching, and high dissolved solids need dilution or a robust interface. Daily tuning, mass calibration and performance checks with a multi-element standard maintain data quality. Add automation and audit trails for regulated environments and monitor collision gas and pump oil.
How do I select the right ICP Time-of-Flight Mass Spectrometer?
Select a time-of-flight instrument when the analysis involves fast transients, many elements recorded simultaneously, or spatial imaging, such as laser ablation or single-particle work. Specify the elements, transient duration and spatial resolution. Confirm that the mass resolution and software processing meet the needs of the study.
How does it compare with other ICP-MS variants?
Select an ICP-MS configuration by the required detection limits, the number of elements, the isotope information needed and the matrix. A single quadrupole with a collision cell handles most routine ultratrace work economically. A triple quadrupole adds reaction-cell mass selection for difficult interferences and low-level sulfur, phosphorus and halogens. High-resolution sector field instruments resolve spectral overlaps and offer higher sensitivity for semiconductor and geochemical work. Multicollector instruments provide the precision needed for isotope ratio studies. Time-of-flight instruments capture the full mass spectrum for rapid multi-element or single-particle analysis. Laser ablation adds direct solid sampling. Match the sample introduction, collision gas and software to your matrices and regulatory requirements.
Full specifications
| Mass range | 2–260 amu |
|---|---|
| Detection limit | 1–100 ng/L typical |
| Analyzer | time of flight |
| Spectra per second | up to 1000 |
| Mass resolution | approximately 1000 |
| Collision cell | optional |
| Plasma power | 1500–1600 W |
| Argon consumption | 15–20 L/min |
| Sample introduction | nebulizer or laser ablation |
| Interface | Ethernet |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Laser ablation elemental imaging
- Single-particle and nanoparticle analysis
- Single-cell multi-element measurement
- Fast transient signals in chromatography
Key features
- Full mass spectrum from each plasma pulse
- Simultaneous detection of all masses
- Ideal for fast transient and single-particle signals
- High acquisition rate for imaging
- Optional collision reaction cell
- Moderate mass resolution compared with sectors
Frequently asked questions about ICP Time-of-Flight Mass Spectrometer
A nanoparticle produces a signal lasting only milliseconds. A scanning instrument could miss or partially sample it, while a time-of-flight analyzer records all masses from each pulse, capturing the complete particle signature. This allows element ratios per particle to be calculated accurately.
Sensitivity per element is somewhat lower than a dedicated quadrupole because the ion beam is shared across the spectrum rather than concentrated on one mass. For transient or imaging work the gains in coverage and speed usually outweigh this, and method optimization can recover much of the difference.
Laser ablation imaging produces large data sets that need software to align ablation tracks, build elemental maps and extract line profiles or region statistics. Fast acquisition requires the software to handle thousands of spectra per second and to export images for further statistical analysis.
Plasma and matrix species form polyatomic ions that share mass with analyte ions, such as argon chloride with arsenic and argon argon with selenium. A cell filled with helium or a reactive gas removes or shifts these interferences before mass analysis, lowering background and improving accuracy at ultratrace levels.
Elements such as mercury, iodine and boron stick to tubing and cones, causing carry-over. Rinsing with dilute acid, adding complexing agents such as gold or ammonia to rinse solutions, and running blanks between samples control memory effects. Method development defines rinse time and composition for each problematic element.
Common internal standards are lithium-6, scandium, germanium, rhodium, indium, terbium, holmium and bismuth, chosen to bracket the mass range of the analytes. They correct for signal drift, matrix suppression and nebulization differences. The standard must not be present in the sample and should have similar ionization behavior.
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