

Quadrupole ICP-MS Spectrometer
四极杆电感耦合等离子体质谱仪
- SKU ICM-0001
- 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 |
| Resolution | 0.3–1.0 amu |
| Collision gas | helium or hydrogen |
| Dynamic range | up to 9 orders |
| Plasma power | 1500–1600 W |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ICH Q3D Elemental Impurities, USP <233> Elemental Impurities — Procedures, USP <730> Plasma Spectrochemistry
What is the Quadrupole ICP-MS Spectrometer?
A quadrupole ICP-MS spectrometer scans selected masses after plasma ionization and usually includes a collision cell. It is the standard, general-purpose choice for routine ultratrace multi-element analysis in most modern research and industrial laboratories.
What is the Quadrupole ICP-MS Spectrometer?
A quadrupole ICP-MS spectrometer scans selected masses after plasma ionization and usually includes a collision cell. It is the standard, general-purpose choice for routine ultratrace multi-element analysis in most modern research and industrial laboratories.
Overview
The quadrupole analyzer consists of four parallel rods that create a radio-frequency and direct-current field, transmitting ions of one mass-to-charge ratio at a time as the voltages scan. Scan speeds of several thousand atomic mass units per second allow rapid multi-element methods. A collision or reaction cell before the analyzer, filled with helium or hydrogen and operated in kinetic energy discrimination mode, removes most polyatomic interferences so elements such as arsenic, selenium and vanadium can be measured in chloride and sulfate matrices. The ion detector uses pulse counting for low signals and analog mode for high signals to cover up to nine orders of magnitude. Sample introduction is by nebulizer and spray chamber, with optional laser ablation or chromatography. This configuration is the workhorse for elemental impurity, environmental and food testing.
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?
- Quadrupole analyzer with rapid mass scanning
- Collision or reaction cell for interference control
- Pulse counting and analog detection modes
- Detection limits in the low nanogram per litre range
- Optional laser ablation and chromatography interfaces
- Automated tuning and performance checks
What are the technical specifications?
A typical quadrupole icp-ms spectrometer configuration offers mass range of 2–260 amu, detection limit of 1–100 ng/L typical, resolution of 0.3–1.0 amu, collision gas of helium or hydrogen, dynamic range of up to 9 orders and plasma power of 1500–1600 W. 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 Quadrupole ICP-MS Spectrometer is used in elemental impurities in pharmaceutical materials, ultratrace metals in water and wastewater, food and feed trace element testing and clinical and forensic 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 Quadrupole ICP-MS Spectrometer?
Select a quadrupole ICP-MS for general ultratrace multi-element work where detection limits of a few nanograms per litre are adequate and cost and simplicity matter. Specify the element list, matrices and required limits, and confirm that the collision cell configuration handles your known interferences. Check argon, vacuum and electrical services.
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 |
| Resolution | 0.3–1.0 amu |
| Collision gas | helium or hydrogen |
| Dynamic range | up to 9 orders |
| Plasma power | 1500–1600 W |
| Argon consumption | 15–20 L/min |
| Scan speed | up to 5000 amu/s |
| 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
- Elemental impurities in pharmaceutical materials
- Ultratrace metals in water and wastewater
- Food and feed trace element testing
- Clinical and forensic trace analysis
Key features
- Quadrupole analyzer with rapid mass scanning
- Collision or reaction cell for interference control
- Pulse counting and analog detection modes
- Detection limits in the low nanogram per litre range
- Optional laser ablation and chromatography interfaces
- Automated tuning and performance checks
Frequently asked questions about Quadrupole ICP-MS Spectrometer
For most elements detection limits are 1 to 100 nanograms per litre, with some elements lower and some higher because of ionization efficiency, background and interferences. The practical limit depends on the blank, matrix and collision cell conditions as much as on the instrument itself.
In kinetic energy discrimination the collision cell is filled with helium, and a small voltage barrier at the cell exit blocks low-energy ions. Large polyatomic ions lose more energy in collisions than small analyte ions, so they are preferentially removed while the analyte passes through. The barrier voltage is tuned during method development.
Yes, with an oxygen addition line and a solvent-resistant sample introduction kit, and with appropriate plasma power. Organic solvents raise the carbon load and can deposit soot, so dedicated nebulizers, spray chambers and torches are used. Flammable solvent safety and ventilation requirements apply.
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.





