

Triple Quadrupole ICP-MS (ICP-MS/MS)
三重四极杆电感耦合等离子体质谱仪(ICP-MS/MS)
- SKU IMS-0002
- ICP-MS
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
- IEC 61010-1 safety (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Mass range | m/z 2–260 |
|---|---|
| Sensitivity (Y 89, no-gas mode) | ≥ 50 Mcps/ppm |
| Abundance sensitivity | ≤ 1×10^-10 (at m/z 89, Q1 + Q2) |
| BEC, sulfur (32S16O, O2 mode) | ≤ 100 ppt |
| BEC, phosphorus (31P16O) | ≤ 50 ppt |
| Oxide ratio (CeO/Ce) | ≤ 1.5% |
By Lab Manufacturers China Technical TeamLast reviewed Standards: USP <233> Elemental Impurities Procedures, ICH Q3D Elemental Impurities, EPA Method 200.8
What is the Triple Quadrupole ICP-MS (ICP-MS/MS)?
An ICP-MS/MS places two quadrupole mass filters around a reaction cell, so only the selected precursor mass enters it. This controlled reaction chemistry removes interferences that helium mode cannot, which suits sulfur, phosphorus, silicon, selenium, arsenic, rare earth elements and high-purity semiconductor analysis.
What is the Triple Quadrupole ICP-MS (ICP-MS/MS)?
An ICP-MS/MS places two quadrupole mass filters around a reaction cell, so only the selected precursor mass enters it. This controlled reaction chemistry removes interferences that helium mode cannot, which suits sulfur, phosphorus, silicon, selenium, arsenic, rare earth elements and high-purity semiconductor analysis.
Overview
In an ICP-MS/MS, the first quadrupole (Q1) filters ions before they enter the octopole reaction cell, so only the target m/z and its same-mass interferences reach the cell. With reaction gases such as oxygen, ammonia or hydrogen, analytes are either shifted to a product-ion mass, for example 32S+ to 32S16O+ at m/z 48, or interferences are neutralized. The second quadrupole (Q2) then selects the product ion. This mass-shift and on-mass reaction control produces reproducible results even when the sample matrix changes, because unwanted ions are rejected before reacting. The approach reaches background equivalent concentrations in the low ppt for sulfur and phosphorus, and supports analysis of isotopes such as 28Si and 31P in high-purity acids. Helium mode remains available for multi-element screening. Cost and tuning complexity are higher than for a single quadrupole instrument.
How does it work?
In ICP-MS, a liquid sample is nebulized into a fine aerosol, passes through a spray chamber, and is carried by argon into a plasma torch. A radio-frequency coil at 27 or 40 MHz sustains a plasma at about 6000 to 10000 K, which desolvates, atomizes and ionizes the analytes, mostly as singly charged ions. Ions are extracted through sampler and skimmer cones into a high-vacuum region, focused by ion lenses, and separated by a mass analyzer, most commonly a quadrupole. A collision or reaction cell removes polyatomic interferences such as 40Ar16O on 56Fe, using helium kinetic energy discrimination or reactive gases. An electron multiplier in pulse and analog modes counts ions across up to nine orders of magnitude.
What are the key features?
- Two quadrupole mass filters around the reaction cell for controlled reaction chemistry
- Mass-shift mode using oxygen or ammonia to move analytes away from interferences
- On-mass mode with hydrogen or helium for conventional interference removal
- Background equivalent concentration at low ppt for sulfur, phosphorus and silicon
- Automated reaction gas tuning and method development assistance in software
- Fast Q1 and Q2 scanning supporting multi-tune methods within one acquisition
What are the technical specifications?
A typical triple quadrupole icp-ms (icp-ms/ms) configuration offers mass range of m/z 2–260, sensitivity (Y 89, no-gas mode) of ≥ 50 Mcps/ppm, abundance sensitivity of ≤ 1×10^-10 (at m/z 89, Q1 + Q2), BEC, sulfur (32S16O, O2 mode) of ≤ 100 ppt, BEC, phosphorus (31P16O) of ≤ 50 ppt and oxide ratio (CeO/Ce) of ≤ 1.5%. 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 (ICP-MS/MS) is used in sulfur, phosphorus and silicon in high-purity materials, semiconductor process chemical analysis, rare earth element analysis in geological samples, selenium and arsenic in complex matrices and nanoparticle analysis by single-particle mode. Across the wider ICP-MS class, laboratories also deploy it for heavy metals in drinking water and wastewater, elemental impurities in pharmaceuticals and toxic elements in food and beverages.
Which standards and certifications apply?
Relevant standards and methods include USP <233> Elemental Impurities Procedures, ICH Q3D Elemental Impurities, EPA Method 200.8, EPA Method 6020B, ISO 17294-2, ASTM D5673, EN 15763, GB 5009.268, ISO/IEC 17025 and IEC 61010-1. Certification candidates for this model are CE, ISO 9001 manufacturing and IEC 61010-1 safety; 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, typically 99.996 percent or better, with consumption around 15 to 20 L per minute, plus cooling water or a recirculating chiller, dedicated exhaust ventilation and stable power. Use trace-metal-grade acids, low-blank labware such as PFA or FEP, and ultrapure water at 18.2 MΩ·cm. Tune daily for sensitivity, oxide ratio (CeO/Ce below 2 percent) and doubly charged ratio (Ce++/Ce below 3 percent). Clean or replace cones, torch and nebulizer according to matrix load, and check the peristaltic pump tubing regularly. Use internal standards to correct drift. For pharmaceutical and regulated work, require software with audit trails and follow USP <233> and ICH Q3D method validation.
How do I select the right Triple Quadrupole ICP-MS (ICP-MS/MS)?
Select ICP-MS/MS when helium mode cannot resolve interferences on S, P, Si, As, Se or REE, or when sample matrices vary unpredictably. Standard quadrupole instruments generally suffice for routine metals work. In an RFQ, specify abundance sensitivity, BEC targets, reaction gases required and automated tuning support.
How does it compare with other ICP-MS variants?
Choose the ICP-MS class by interference severity, detection limit and budget. A single quadrupole with a collision cell handles most water, food and clinical work at low cost. Triple quadrupole ICP-MS/MS adds mass-shift reaction chemistry for difficult interferences such as sulfur, phosphorus, arsenic in chloride and rare earth oxides. Sector-field instruments offer high resolution and the lowest background for semiconductor and geochemical work, and TOF systems capture the full mass spectrum for fast transient signals. Check matrix tolerance, for example total dissolved solids up to 0.2 percent or aerosol dilution options for higher levels, argon consumption, sample introduction kits, autosampler and software compliance features. Verify the detection limits and background equivalent concentrations in your own matrix rather than relying on deionized water values.
Full specifications
| Mass range | m/z 2–260 |
|---|---|
| Sensitivity (Y 89, no-gas mode) | ≥ 50 Mcps/ppm |
| Abundance sensitivity | ≤ 1×10^-10 (at m/z 89, Q1 + Q2) |
| BEC, sulfur (32S16O, O2 mode) | ≤ 100 ppt |
| BEC, phosphorus (31P16O) | ≤ 50 ppt |
| Oxide ratio (CeO/Ce) | ≤ 1.5% |
| Reaction gases | O2, NH3/He, H2, He |
| Detector dynamic range | 10 orders of magnitude |
| Stability (RSD, 2 h) | ≤ 3% |
| Argon consumption | ~15–18 L/min |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Sulfur, phosphorus and silicon in high-purity materials
- Semiconductor process chemical analysis
- Rare earth element analysis in geological samples
- Selenium and arsenic in complex matrices
- Nanoparticle analysis by single-particle mode
Key features
- Two quadrupole mass filters around the reaction cell for controlled reaction chemistry
- Mass-shift mode using oxygen or ammonia to move analytes away from interferences
- On-mass mode with hydrogen or helium for conventional interference removal
- Background equivalent concentration at low ppt for sulfur, phosphorus and silicon
- Automated reaction gas tuning and method development assistance in software
- Fast Q1 and Q2 scanning supporting multi-tune methods within one acquisition
Frequently asked questions about Triple Quadrupole ICP-MS (ICP-MS/MS)
In mass-shift mode, Q1 selects the analyte mass, a reaction gas such as oxygen converts the analyte to a product ion of higher mass, and Q2 measures that product. Interferences at the original mass do not form the same product, so they are avoided.
S and P suffer from O2+ and NO+ interferences and high background. With oxygen mass-shift, S and P form SO+ and PO+ at m/z 48 and 47 where interferences are largely absent, and Q1 prevents other ions from forming the same product, giving lower background.
No significant loss for most elements in no-gas or helium mode. In reaction mode, sensitivity depends on reaction efficiency, which for oxygen or ammonia mass-shift can exceed 90 percent for many analytes. Lower absolute counts are compensated by much lower background.
ICP-MS typically reaches low parts-per-trillion (ng/L) detection limits for most elements in clean aqueous solutions, and sub-ppt for some heavy elements. Real-world limits are higher because of sample dilution, blank contamination and matrix effects, so they must be established by method validation.
ICP-OES measures light emitted by excited atoms and ions, reaching ppb detection limits over a wide linear range and high matrix tolerance. ICP-MS measures ions by mass, reaching ppt limits, and provides isotope information, but it tolerates fewer dissolved solids and costs more to operate.
In helium kinetic energy discrimination mode, larger polyatomic ions collide more often with helium and lose more energy than analyte ions, so a bias voltage blocks them. Reactive gases such as oxygen or ammonia can instead convert the analyte or the interference to a different mass.
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