
Krypton Low-Surface-Area Analyzer for Thin Films and Flat Substrates
薄膜与平整基底用氪气低比表面积分析仪
- CE (to be confirmed)
- +1
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微孔与介孔分析用高真空容量法物理吸附分析仪
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Prices depend on configuration, quantity and destination port.
| Measurement principle | Static volumetric physisorption |
|---|---|
| Surface area range | 0.01 m²/g to no upper limit |
| Pore size range | 0.35–500 nm |
| Analysis gases | N₂, Ar, Kr, CO₂ |
| Pressure transducers | 0.1, 10, 1000 torr |
| Ultimate vacuum | ≤ 5×10⁻⁸ torr |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 9277, ISO 15901-2, ISO 15901-3
A static volumetric analyzer with turbomolecular pumping and low-pressure transducers that records full nitrogen or argon isotherms down to about 10⁻⁶ relative pressure. It is the right choice for BET area plus micropore and mesopore distribution in zeolites, carbons and frameworks.
A static volumetric analyzer with turbomolecular pumping and low-pressure transducers that records full nitrogen or argon isotherms down to about 10⁻⁶ relative pressure. It is the right choice for BET area plus micropore and mesopore distribution in zeolites, carbons and frameworks.
This variant uses a high-vacuum manifold with a turbomolecular pump and several pressure transducers of different ranges, typically 0.1, 10 and 1000 torr, so that very low relative pressures can be reached accurately. Low-pressure dosing in small increments resolves the micropore filling region below 2 nm, which is essential for zeolites, activated carbons and metal-organic frameworks. Analysis uses BET, t-plot, Dubinin–Radushkevich, BJH and non-local density functional theory with suitable kernels. Systems commonly offer two to four analysis ports, independent degassing stations and a liquid nitrogen or cryostat bath. A full micropore isotherm can take 20 to 60 hours, so the instrument is usually automated with a level-controlled Dewar and a saturation pressure monitor.
These analyzers expose a degassed solid to an adsorbate and measure how much is taken up. In static volumetric physisorption, known doses of nitrogen, argon or krypton are admitted to a manifold and sample tube at 77 K or 87 K, and the pressure drop after equilibration gives the adsorbed volume. Isotherms are analyzed with BET for surface area, t-plot and DFT methods for micropores, and BJH for mesopores. Gravimetric systems weigh the sample directly while vapor pressure is controlled. Chemisorption analyzers dose hydrogen, CO or oxygen at elevated temperature and use thermal conductivity detection for temperature-programmed reduction and desorption. Key components are vacuum pumps, pressure transducers, a cryogenic bath or furnace, and analysis software.
A typical high-vacuum volumetric physisorption analyzer for micropore and mesopore analysis configuration offers measurement principle of Static volumetric physisorption, surface area range of 0.01 m²/g to no upper limit, pore size range of 0.35–500 nm, analysis gases of N₂, Ar, Kr, CO₂, pressure transducers of 0.1, 10, 1000 torr and ultimate vacuum of ≤ 5×10⁻⁸ torr. 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.
The High-Vacuum Volumetric Physisorption Analyzer for Micropore and Mesopore Analysis is used in zeolite and MOF micropore analysis, activated carbon characterization, catalyst support pore structure and battery carbon and silicon anode materials. Across the wider Surface Area Analyzers class, laboratories also deploy it for catalyst and support characterization, battery electrode powder analysis and activated carbon and adsorbent testing.
Relevant standards and methods include ISO 9277, ISO 15901-2, ISO 15901-3, ASTM D3663 and ASTM D4365. Certification candidates for this model are CE, ISO 9001 manufacturing and RoHS; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Sample degassing is the main source of error; select temperature and time so that moisture and volatiles are removed without changing the structure, and weigh the sample after degassing. Use adequate sample mass to provide at least 1 m² of total surface area, or 0.05 m² with krypton. Check free-space calibration and leak rates regularly. Ensure a reliable supply of high-purity gases, typically 99.999 percent, and monitor liquid nitrogen levels. Verify performance with certified reference materials of known surface area. Place the unit on a stable bench with ventilation for cryogenic and hydrogen work, and follow local rules for compressed gas cylinders.
Select this variant when micropore volume or sub-2 nm pore size distribution is a reported value, or when laboratory work involves porous framework research. For routine area checks above 1 m²/g, a lower-cost station without turbomolecular pumping is adequate. In an RFQ, specify the lowest relative pressure needed, number of ports, analysis gases, DFT kernels and degassing temperature limit.
Decide first what must be measured. Surface area and mesopore size of powders, catalysts and electrode materials suit a volumetric physisorption analyzer; micropore work requires turbomolecular pumping and low-pressure transducers. Very low area films and substrates need krypton capability. Water or solvent uptake calls for a gravimetric vapor sorption analyzer. Metal dispersion and acid site measurements need a chemisorption system with a furnace and detector. Hydrogen and methane storage research needs a high-pressure sorption analyzer. Compare the number of analysis ports, degassing stations, pressure range, transducer accuracy, liquid nitrogen consumption and compliance with ISO 9277 and ISO 15901-2 when specifying.
| Measurement principle | Static volumetric physisorption |
|---|---|
| Surface area range | 0.01 m²/g to no upper limit |
| Pore size range | 0.35–500 nm |
| Analysis gases | N₂, Ar, Kr, CO₂ |
| Pressure transducers | 0.1, 10, 1000 torr |
| Ultimate vacuum | ≤ 5×10⁻⁸ torr |
| Analysis ports | 2–4 |
| Degassing stations | 2–6, up to 400 °C |
| Transducer accuracy | ±0.12% of reading |
| Power supply | 220 V, 50/60 Hz |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Micropore filling occurs at relative pressures below 10⁻³, where absolute pressures are a few millitorr. A turbomolecular pump provides the clean, deep vacuum and fast evacuation needed to dose accurately and avoid contamination at those pressures.
A full nitrogen isotherm from 10⁻⁷ to 0.99 relative pressure typically takes 20 to 60 hours depending on equilibration criteria and sample. Mesoporous samples with only BET and BJH analysis are commonly completed in 2 to 6 hours.
Yes. Argon at 87 K is preferred for zeolites and some oxides because it has no quadrupole interaction with surface groups, giving micropore filling at higher relative pressure and a more reliable pore size from DFT kernels.
A BET analyzer measures gas adsorption on a solid at cryogenic temperature and applies the Brunauer–Emmett–Teller model to calculate specific surface area in m²/g. Most instruments also give pore volume and pore size distribution from the same isotherm.
Degassing removes water, solvents and adsorbed gases that would otherwise occupy the surface and bias the measured area. Temperature and time depend on the material, for example 150–300 °C for many oxides, and must not collapse the pore structure.
Not usually. Physisorption analyzers measure area and pores using nitrogen at 77 K, while metal dispersion requires chemisorption of hydrogen or CO at controlled temperatures with a furnace and detector. Some combined platforms offer both modules in one cabinet.

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