

Simultaneous Multi-Element ICP-OES Spectrometer
多元素同时测定 ICP-OES 光谱仪
- SKU ICO-0004
- ICP-OES
- 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
| Wavelength range | 165–900 nm |
|---|---|
| Detection | simultaneous array |
| Detector | CCD or CMOS array |
| Simultaneous elements | up to 70 |
| Analysis time | 10–30 s per sample |
| Detection limit | 0.5–10 µg/L typical |
By Lab Manufacturers China Technical TeamLast reviewed Standards: USP <730> Plasma Spectrochemistry, USP <233> Elemental Impurities — Procedures, ICH Q3D Elemental Impurities
What is the Simultaneous Multi-Element ICP-OES Spectrometer?
A simultaneous ICP-OES spectrometer records many wavelengths at once with a large array detector and no scanning. It is chosen for busy high-throughput laboratories that measure large element panels in a single fast reading.
What is the Simultaneous Multi-Element ICP-OES Spectrometer?
A simultaneous ICP-OES spectrometer records many wavelengths at once with a large array detector and no scanning. It is chosen for busy high-throughput laboratories that measure large element panels in a single fast reading.
Overview
This instrument uses a fixed echelle or similar polychromator with a large CCD or CMOS array, so light at all the analytical wavelengths falls on the detector simultaneously and is read in one integration. Every element and line in the method is acquired at once, which reduces analysis time to a few seconds per sample and improves precision because all lines share the same plasma conditions. The design is well suited to large element panels, such as full impurity screens or multi-element water methods, and to laboratories with high sample numbers. Because the wavelength positions are fixed by calibration rather than scanned, stability of the optics is critical, and periodic wavelength calibration is required. Detector segmenting and dynamic range management handle both weak and strong lines. The approach pairs naturally with autosamplers and with internal standard correction.
How does it work?
A radio-frequency generator drives a load coil around a quartz torch, sustaining an argon plasma at 6000 to 10000 K. The sample aerosol enters the plasma and is desolvated, vaporized, atomized and excited. Excited atoms and ions relax and emit light at wavelengths characteristic of each element. The emitted light is dispersed by an echelle grating or a CCD-based polychromator, and multiple lines are measured simultaneously. In radial viewing the plasma is observed from the side, which tolerates high dissolved solids and reduces self-absorption; in axial viewing the plasma is observed end-on, which lengthens the optical path and lowers detection limits. Dual-view instruments switch per element. Internal standards, background correction and interference algorithms correct for drift and overlapping lines. The wide dynamic range lets major, minor and trace elements be measured in one run.
What are the key features?
- Fixed polychromator with large array detector
- All analytical wavelengths acquired in one integration
- Few seconds per sample for large element panels
- Improved precision from shared plasma conditions
- Periodic wavelength calibration for fixed optics
- Internal standard and dynamic range correction
What are the technical specifications?
A typical simultaneous multi-element icp-oes spectrometer configuration offers wavelength range of 165–900 nm, detection of simultaneous array, detector of CCD or CMOS array, simultaneous elements of up to 70, analysis time of 10–30 s per sample and detection limit of 0.5–10 µg/L typical. 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 Simultaneous Multi-Element ICP-OES Spectrometer is used in full elemental impurity panels, large multi-element water methods, food and feed multi-element screening and high-throughput contract analysis. Across the wider ICP-OES class, laboratories also deploy it for multi-element water and wastewater analysis, pharmaceutical elemental impurity screening and food, feed and agricultural element analysis.
Which standards and certifications apply?
Relevant standards and methods include USP <730> Plasma Spectrochemistry, USP <233> Elemental Impurities — Procedures, ICH Q3D Elemental Impurities, ISO 11885 Water quality — ICP-OES determination of elements, US EPA Method 200.7, ASTM D5185 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-OES requires high-purity argon, substantial power, exhaust ventilation and a temperature-controlled room. Torch, injector and nebulizer condition strongly affect performance, so inspection and replacement schedules are important. High dissolved solids cause salt build-up on the torch and injector, blocking the plasma and changing sensitivity, so dilution and matrix matching are used. Sample preparation by acid digestion must avoid contamination. Daily checks include wavelength calibration, torch alignment, plasma stability and a check standard. Monitor the argon supply and the chiller, and record torch and nebulizer usage. Data integrity requires calibration verification, QC samples and defined acceptance criteria.
How do I select the right Simultaneous Multi-Element ICP-OES Spectrometer?
Select a simultaneous instrument when methods contain many elements and lines and sample numbers are high, because per-sample time dominates cost. Specify the element panel, required detection limits and throughput, and confirm that the fixed wavelength coverage includes all your lines. Periodic wavelength calibration and optical stability checks are essential.
How does it compare with other ICP-OES variants?
Select an ICP-OES spectrometer by viewing configuration, detector type, resolution and automation. Radial viewing is the best choice for high-matrix samples and major elements, axial viewing for the lowest detection limits in clean samples, and dual view for laboratories that handle both. Simultaneous CCD instruments measure many elements and lines quickly, while sequential scanning instruments are flexible and lower in cost but slower. High-resolution echelle optics help when many emission lines overlap, as in rare-earth or iron-rich samples. Confirm the wavelength range covers the elements and lines you need, including far-ultraviolet lines for halogens. Check argon and power consumption, sample introduction options, autosampler capacity and software features such as interference correction and audit trails.
Full specifications
| Wavelength range | 165–900 nm |
|---|---|
| Detection | simultaneous array |
| Detector | CCD or CMOS array |
| Simultaneous elements | up to 70 |
| Analysis time | 10–30 s per sample |
| Detection limit | 0.5–10 µg/L typical |
| Optical resolution | ≤ 0.009 nm at 200 nm |
| RF power | 1000–1500 W |
| Argon consumption | 14–18 L/min |
| Autosampler | up to 240 positions |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Full elemental impurity panels
- Large multi-element water methods
- Food and feed multi-element screening
- High-throughput contract analysis
Key features
- Fixed polychromator with large array detector
- All analytical wavelengths acquired in one integration
- Few seconds per sample for large element panels
- Improved precision from shared plasma conditions
- Periodic wavelength calibration for fixed optics
- Internal standard and dynamic range correction
Frequently asked questions about Simultaneous Multi-Element ICP-OES Spectrometer
Once the plasma is stable and the autosampler delivers the sample, a full element panel is usually acquired in 10 to 30 seconds, including rinse and integration. Additional lines for confirmation or interference checks add little time because they are recorded simultaneously.
The detector has fixed pixel-to-wavelength assignments, so thermal drift or mechanical movement shifts lines off their expected positions and causes errors. Periodic wavelength calibration with a standard solution restores alignment, and some instruments monitor an internal reference line continuously.
Not for most elements, because all lines are integrated over the same dwell time and there is no scanning overhead. Very weak lines may benefit from longer integration, which a simultaneous instrument can still provide by increasing acquisition time for the whole set. Sensitivity mainly depends on the optical design.
Radial viewing observes a thin section of the plasma, which reduces self-absorption and tolerates high dissolved solids and major elements without saturating the detector. Axial viewing looks through the plasma length for lower detection limits in clean samples. Dual-view instruments combine both, and the operator selects the view per element.
Excited atoms and ions have many energy levels, so each element emits numerous lines, some strong and some weak. The analyst selects a line free from overlap and within the working range for the expected concentration. Weak lines suit high concentrations, and strong lines suit trace levels.
Yes, in principle, using far-ultraviolet emission lines, for example chlorine at 134.7 and 135.2 nanometres, bromine and iodine lines, and sulfur and phosphorus lines. These lines require a vacuum or purged optical path because air absorbs far-ultraviolet light. Sensitivity is lower than for metals, and ICP-MS may be preferred.




