

Ultrasonic Nebulizer Sample Introduction System
超声雾化样品引入系统
- SKU ISI-0002
- ICP Sample Introduction Systems
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
- Elemental cleanliness test (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Nebulizer type | ultrasonic, piezoelectric |
|---|---|
| Frequency | 1–3 MHz |
| Transport efficiency | 10–40% |
| Sample uptake rate | 0.5–2 mL/min |
| Desolvation temperature | 120–160 °C |
| Condenser | Peltier or water cooled |
By Lab Manufacturers China Technical TeamLast reviewed Standards: USP <730> Plasma Spectrochemistry, ISO 11885 Water quality — ICP-OES determination of elements, US EPA Method 200.7
What is the Ultrasonic Nebulizer Sample Introduction System?
An ultrasonic nebulizer sample introduction system uses a vibrating transducer to create a fine aerosol. It is chosen for trace analysis of clean samples when lower detection limits justify extra sample consumption and complexity.
What is the Ultrasonic Nebulizer Sample Introduction System?
An ultrasonic nebulizer sample introduction system uses a vibrating transducer to create a fine aerosol. It is chosen for trace analysis of clean samples when lower detection limits justify extra sample consumption and complexity.
Overview
A piezoelectric transducer vibrating at high frequency converts the liquid sample into a dense, fine aerosol with a higher proportion of small droplets than a pneumatic nebulizer. A heated tube and condenser desolvate the aerosol, removing water vapor so that a concentrated dry aerosol enters the plasma. Transport efficiency rises to tens of percent, lowering detection limits by roughly five to ten times for many elements. The system consumes more sample, typically 0.5 to 2 millilitres per minute, and requires heating and cooling, adding maintenance. High dissolved solids can deposit on the transducer and desolvation tube, so samples are usually diluted. It is used for ultratrace water analysis, geological and biological samples where detection limits are the priority.
How does it work?
The sample introduction system determines how much sample reaches the plasma and in what form. For liquids, a peristaltic pump delivers sample to a nebulizer, which creates an aerosol; a spray chamber then removes large droplets so only fine droplets enter the plasma. Nebulizer type and spray chamber design set transport efficiency, which is typically only a few percent, and thus sensitivity. Ultrasonic nebulizers use vibration to produce finer aerosols and improve transport, while electrothermal vaporization heats a small sample to form a vapor. Hydride generation converts certain elements into volatile species, separating them from the matrix. Laser ablation removes solid particles from a sample surface for direct analysis. Whichever approach is used, transport tubing length and gas flows must be optimized, and washout between samples controls carry-over.
What are the key features?
- Piezoelectric transducer for fine dense aerosol
- Heated desolvation tube and condenser
- Transport efficiency of tens of percent
- Detection limits five to ten times lower
- Higher sample consumption and maintenance
- Suited to clean samples and ultratrace work
What are the technical specifications?
A typical ultrasonic nebulizer sample introduction system configuration offers nebulizer type of ultrasonic, piezoelectric, frequency of 1–3 MHz, transport efficiency of 10–40%, sample uptake rate of 0.5–2 mL/min, desolvation temperature of 120–160 °C and condenser of Peltier or water cooled. 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 Ultrasonic Nebulizer Sample Introduction System is used in ultratrace metals in drinking water, geological and environmental trace analysis, biological and clinical trace elements and reference material characterization. Across the wider ICP Sample Introduction Systems class, laboratories also deploy it for routine liquid sample delivery for ICP-OES and ICP-MS, trace analysis with improved transport efficiency and direct solid sampling and elemental mapping.
Which standards and certifications apply?
Relevant standards and methods include USP <730> Plasma Spectrochemistry, ISO 11885 Water quality — ICP-OES determination of elements, US EPA Method 200.7, US EPA Method 200.8, US EPA Method 6020B and ISO/IEC 17025. Certification candidates for this model are CE, ISO 9001 manufacturing and Elemental cleanliness test; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Sample introduction components are the most frequently replaced parts of an ICP system and are the usual cause of reduced sensitivity or precision. Nebulizers clog, corrode or crack; spray chambers accumulate deposits; pump tubing stretches and changes flow; and laser cells and transport lines adsorb analytes. Establish cleaning and replacement schedules and keep spares. Transport efficiency depends on gas flow, tubing length and chamber design, so changing one component may require method reoptimization. For high-solids samples, dilute or use a matrix-tolerant nebulizer to avoid blockages. Always check uptake rate and aerosol quality after maintenance, and verify performance with a check standard before releasing results.
How do I select the right Ultrasonic Nebulizer Sample Introduction System?
Select an ultrasonic nebulizer when detection limits are the deciding factor and samples are clean and available in sufficient volume. Specify the elements, target limits and matrix. Confirm that dilution will not defeat the sensitivity gain, and budget for the heated desolvation components and their maintenance.
How does it compare with other ICP Sample Introduction Systems variants?
Select a sample introduction system by sample type, detection limit requirements and matrix. A concentric nebulizer with a cyclonic spray chamber is the standard, efficient choice for clean aqueous solutions. High dissolved solids need a V-groove, cross-flow or high-solids nebulizer that resists blockage. Ultrasonic nebulization improves detection limits for trace work when sample volume allows. Laser ablation is chosen for solid samples and spatial mapping, and electrothermal vaporization for very small volumes or micro-samples. Hydride generation targets arsenic, selenium and related elements with matrix separation. Autosamplers with peristaltic pumps provide reproducible delivery and throughput. Confirm compatibility with your torch, plasma gas flows and instrument software.
Full specifications
| Nebulizer type | ultrasonic, piezoelectric |
|---|---|
| Frequency | 1–3 MHz |
| Transport efficiency | 10–40% |
| Sample uptake rate | 0.5–2 mL/min |
| Desolvation temperature | 120–160 °C |
| Condenser | Peltier or water cooled |
| Detection limit improvement | 5–10 times lower |
| Dissolved solids tolerance | up to 0.2% |
| Washout time | 40–90 s |
| Compatible instruments | ICP-OES and ICP-MS |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Ultratrace metals in drinking water
- Geological and environmental trace analysis
- Biological and clinical trace elements
- Reference material characterization
Key features
- Piezoelectric transducer for fine dense aerosol
- Heated desolvation tube and condenser
- Transport efficiency of tens of percent
- Detection limits five to ten times lower
- Higher sample consumption and maintenance
- Suited to clean samples and ultratrace work
Frequently asked questions about Ultrasonic Nebulizer Sample Introduction System
Because transport efficiency can rise from a few percent to tens of percent, detection limits typically improve by five to ten times for clean aqueous samples. The gain is largest for elements with low background and least for elements limited by contamination or by the blank rather than by transport.
The dense aerosol carries a large amount of water into the plasma, which would cool it, destabilize it and increase oxide and hydroxide interferences. Heating the aerosol and condensing the vapor removes most water before it reaches the plasma, so a dry, concentrated aerosol is analyzed.
The transducer surface and desolvation tube require regular cleaning to remove salt deposits, and the heating and cooling components need periodic checking. Transducers have a limited life and must be replaced when efficiency drops. Uptake rate and signal response are checked after cleaning.
A pneumatic nebulizer produces droplets of many sizes, and the spray chamber removes most of them to prevent solvent overload and plasma instability. Only a few percent of the sample reaches the plasma. This is why nebulizer and spray chamber design, and the resulting fine aerosol fraction, strongly affect sensitivity.
V-groove, cross-flow, Babington or parallel-path nebulizers tolerate high salt content better than concentric designs because they have wider orifices and resist blockage. A heated spray chamber and dilution also help. Dedicated high-solids kits reduce maintenance and improve long-term stability.
Ultrasonic nebulization produces a finer aerosol and improves transport efficiency, lowering detection limits by roughly five to ten times for clean samples. It uses more sample volume and needs desolvation, and it is more affected by high dissolved solids, so it suits trace analysis of relatively clean solutions.
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