
High-Vacuum Volumetric Physisorption Analyzer for Micropore and Mesopore Analysis
微孔与介孔分析用高真空容量法物理吸附分析仪
- CE (to be confirmed)
- +2
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氢气与二氧化碳储存研究用高压气体吸附分析仪
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Prices depend on configuration, quantity and destination port.
| Maximum pressure | 100 bar (200 bar optional) |
|---|---|
| Temperature range | 77–500 K |
| Adsorbates | H₂, CH₄, CO₂, N₂, He |
| Pressure transducer accuracy | ±0.05% of full scale |
| Sample mass | 0.1–5 g |
| Temperature stability | ±0.05 K |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 9277, ISO 15901-2, ISO 15901-3
A volumetric or gravimetric sorption analyzer rated for gas pressures up to 100 bar or more, measuring excess and total uptake of hydrogen, methane and CO₂. It is used to screen storage and capture materials such as MOFs, carbons and zeolites under practical conditions.
A volumetric or gravimetric sorption analyzer rated for gas pressures up to 100 bar or more, measuring excess and total uptake of hydrogen, methane and CO₂. It is used to screen storage and capture materials such as MOFs, carbons and zeolites under practical conditions.
Standard physisorption analyzers stop near ambient pressure, but storage and capture materials are judged at 10 to 100 bar. This variant uses stainless steel manifolds, high-pressure valves and transducers rated up to 100 or 200 bar, with a thermostatted sample cell from cryogenic temperatures to about 500 K. Volumetric versions apply real-gas equations of state, such as those from NIST REFPROP, to calculate the dose, while gravimetric versions use a magnetic suspension balance that weighs the sample in the pressurized gas and correct for buoyancy. Results are reported as excess uptake and, when skeletal density is known, absolute uptake. Helium calibration determines void volume. Accuracy depends strongly on temperature stability and gas purity, typically 99.9999 percent for hydrogen.
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-pressure gas adsorption analyzer for hydrogen and carbon dioxide storage configuration offers maximum pressure of 100 bar (200 bar optional), temperature range of 77–500 K, adsorbates of H₂, CH₄, CO₂, N₂, He, pressure transducer accuracy of ±0.05% of full scale, sample mass of 0.1–5 g and temperature stability of ±0.05 K. 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-Pressure Gas Adsorption Analyzer for Hydrogen and Carbon Dioxide Storage is used in hydrogen storage material screening, CO₂ capture sorbent evaluation, methane storage in porous carbons and gas separation selectivity studies. 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, Pressure equipment conformity and ISO 9001 manufacturing; 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 uptake at 10 to 100 bar and variable temperature is the required result, typical for gas storage and capture research. Standard analyzers cannot measure these conditions. In an RFQ, specify maximum pressure, gases, temperature range, volumetric versus gravimetric principle, hydrogen safety provisions and local pressure equipment requirements.
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.
| Maximum pressure | 100 bar (200 bar optional) |
|---|---|
| Temperature range | 77–500 K |
| Adsorbates | H₂, CH₄, CO₂, N₂, He |
| Pressure transducer accuracy | ±0.05% of full scale |
| Sample mass | 0.1–5 g |
| Temperature stability | ±0.05 K |
| Uptake resolution | ≤ 0.01 wt% at 100 bar |
| Leak rate | < 10⁻⁸ mbar·L/s |
| Degassing temperature | Up to 500 °C under vacuum |
| Gas purity required | ≥ 99.9999% for H₂ |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Excess uptake is the measured amount beyond what the free gas would occupy in the pore volume. Absolute uptake adds the gas in the adsorbed layer volume and requires an estimate of adsorbed phase density, so excess values are usually reported as primary data.
Helium adsorbs negligibly at most temperatures, so its expansion into the sample cell gives the void volume. The measured value is used to calculate the free gas amount in later hydrogen or CO₂ doses, making helium calibration central to accuracy.
Important features include rated pressure components, rupture discs vented to a safe exhaust, hydrogen leak sensors, automatic shutoff valves, limited gas inventory and adequate ventilation. The installation should be reviewed against local pressure and flammable gas regulations.
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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