

Triple-Quadrupole ICP-MS Spectrometer
三重四极杆电感耦合等离子体质谱仪
- SKU ICM-0002
- 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 | 1–50 ng/L typical |
| Analyzers | two quadrupoles |
| Reaction gases | oxygen, ammonia, hydrogen |
| Modes | single, collision, reaction |
| Dynamic range | up to 9 orders |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ICH Q3D Elemental Impurities, USP <233> Elemental Impurities — Procedures, USP <730> Plasma Spectrochemistry
What is the Triple-Quadrupole ICP-MS Spectrometer?
A triple-quadrupole ICP-MS adds a reaction cell between two mass filters for interference-free measurement. It is chosen for difficult matrices and for elements such as sulfur, phosphorus and halogens at low levels.
What is the Triple-Quadrupole ICP-MS Spectrometer?
A triple-quadrupole ICP-MS adds a reaction cell between two mass filters for interference-free measurement. It is chosen for difficult matrices and for elements such as sulfur, phosphorus and halogens at low levels.
Overview
This instrument places a pressurized reaction cell between two quadrupole mass filters. The first quadrupole transmits only the target ion mass, the cell reacts it with a gas such as oxygen, ammonia or hydrogen to form a new ion, and the second quadrupole selects the product ion for detection. This tandem mass spectrometry approach eliminates the original polyatomic interference because ions of the same mass as the analyte do not form the same product. It enables measurement of elements that are otherwise impossible at low levels, including sulfur, phosphorus, chlorine and silicon, and improves accuracy for arsenic, selenium and other elements in complex matrices. The technique is powerful but requires careful reaction gas selection and tuning, and throughput may be slightly lower than a single quadrupole.
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?
- Reaction cell between two mass filters
- Tandem mass selection of product ions
- Measures sulfur, phosphorus, chlorine and silicon
- Eliminates original polyatomic interferences
- Improves accuracy in difficult matrices
- Requires careful reaction gas tuning
What are the technical specifications?
A typical triple-quadrupole icp-ms spectrometer configuration offers mass range of 2–260 amu, detection limit of 1–50 ng/L typical, analyzers of two quadrupoles, reaction gases of oxygen, ammonia, hydrogen, modes of single, collision, reaction and dynamic range of up to 9 orders. 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 Triple-Quadrupole ICP-MS Spectrometer is used in sulfur and phosphorus in fuels and polymers, halogen and silicon determination, ultratrace impurities in complex drug matrices and environmental and food trace analysis. 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 Triple-Quadrupole ICP-MS Spectrometer?
Select a triple-quadrupole instrument when the element list includes sulfur, phosphorus, halogens or silicon, or when interferences in the matrix cannot be solved with a single collision cell. Specify the target elements, matrices and reaction gas requirements. Confirm method development support, since reaction pathways must be validated.
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 | 1–50 ng/L typical |
| Analyzers | two quadrupoles |
| Reaction gases | oxygen, ammonia, hydrogen |
| Modes | single, collision, reaction |
| Dynamic range | up to 9 orders |
| Plasma power | 1500–1600 W |
| Argon consumption | 15–20 L/min |
| Sample introduction | nebulizer and spray chamber |
| 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
- Sulfur and phosphorus in fuels and polymers
- Halogen and silicon determination
- Ultratrace impurities in complex drug matrices
- Environmental and food trace analysis
Key features
- Reaction cell between two mass filters
- Tandem mass selection of product ions
- Measures sulfur, phosphorus, chlorine and silicon
- Eliminates original polyatomic interferences
- Improves accuracy in difficult matrices
- Requires careful reaction gas tuning
Frequently asked questions about Triple-Quadrupole ICP-MS Spectrometer
Sulfur, phosphorus, chlorine, bromine, iodine and silicon suffer severe polyatomic interferences in a single quadrupole because their masses coincide with plasma and matrix species. Tandem mass selection removes those interferences by detecting a reaction product ion rather than the original ion.
Oxygen is used for elements that form oxide product ions, such as sulfur, phosphorus and arsenic, moving detection to a clean mass. Ammonia and hydrogen promote charge transfer or cluster formation for other elements. Gas choice depends on the analyte and the interferences present and is fixed after method development.
Measurement of a product ion requires additional reaction time and mass selection, so per-element time can be slightly longer. However, complex interferences are removed without extensive correction equations, which often makes overall method development and validation faster and more reliable.
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.





