Product Features
- Dynamic O₂ leak rate as low as 0.09 μmol/h, delivering a threefold improvement in airtightness over conventional systems.
- Calibration-curve linear regression coefficient of R² > 0.999.
- RSD < 2.5% across four consecutive injections at the same concentration.
- Between-system reproducibility deviation of < 5%, supporting consistent data across instruments.
- Multiple reactor configurations are available for a broad range of application scenarios.
- Intelligent touchscreen control simplifies setup, operation, monitoring, and data management.
NO. 1High-Airtightness Design for Reliable Data
The system uses borosilicate-glass reaction piping and precision-lapped glass valves. It achieves an absolute vacuum pressure of ≤ 0.5 kPa and a dynamic O₂ leak rate as low as 0.09 μmol/h, providing three times the airtightness of conventional systems and meeting the stringent requirements of apparent-quantum-yield measurements for photocatalytic overall water splitting. Stable airtightness is maintained even during continuous operation beyond 24 hours, minimizing underestimation of hydrogen evolution caused by gas leakage.
NO. 2Precise Trace-Gas Sampling for Accurate Injection
A patented sampling valve manifold and interchangeable 0.5–5 mL sample loops provide a maximum sampling ratio of 1:88, enabling accurate detection of trace hydrogen generated during the initial stage of a catalytic reaction. The calibration curve delivers R² > 0.999; four consecutive injections at the same concentration achieve RSD < 2.5%; and between-system reproducibility deviation remains below 5%, ensuring accurate, stable, and highly consistent results.
NO. 3Intelligent Touchscreen Control for Greater Efficiency
The integrated control unit features a 7-inch LCD touchscreen. Users can program multistage illumination–dark cycles and automatically collect gas samples at defined time points. For catalyst-stability studies, the system can operate continuously for 100 hours, sample automatically at preset intervals, and capture a complete long-term stability data set, substantially improving experimental efficiency.
Application Fields
- Photocatalytic and Photoelectrocatalytic CO₂ Reduction
- Photocatalytic Apparent Quantum Yield Measurement
- Photocatalytic Overall Water Splitting
- Photocatalytic Oxygen-Evolution Rate Measurement
- Photocatalytic Hydrogen Production
- Photoelectrochemical Water Splitting
- Electrocatalytic Water Splitting
Product Parameters
| μGAS1001 Product Parameters | |||
|---|---|---|---|
| Touchscreen Control Unit | |||
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| System Piping | |||
| Absolute Vacuum Pressure | ≤ 0.5 kPa, referenced to absolute zero to prevent apparent fluctuations caused by changes in temperature, humidity, and other environmental conditions. | Operating Pressure Range | 0 kPa to atmospheric pressure |
| Dynamic O₂ Leak Rate | As low as 0.09 μmol/h; airtightness is improved threefold over conventional products and meets apparent-quantum-yield measurement requirements for photocatalytic overall water splitting. | Piping Material | Highly chemically inert, non-adsorptive borosilicate glass |
| Valve Technology | Precision-lapped borosilicate-glass construction with no metal components | Number of Valves | 3 |
| Vacuum Grease | Imported Apiezon H high-temperature vacuum grease with chemical resistance, low vapor pressure, and low volatility; operating range: −10 to +200 °C | Total System Volume | 440 mL; total reactor volume: 210 mL; recommended working volume: 40–80 mL |
| Piping Temperature Control | Both circulation and injection lines are temperature-controlled, up to 200 °C. | Condenser | Provides sufficient condensation to prevent water vapor from entering the gas chromatograph or vacuum pump, helping protect equipment service life. |
| Fully Automatic Sampling and Injection Module | |||
| Sampling Method | The module is integrated into the system rather than the chromatograph, shortening the circulation path and improving gas-circulation efficiency. | Sample Loop | Standard 2 mL loop; optional 0.5, 1, 3, and 5 mL loops provide adjustable detection sensitivity. |
| Maximum Sampling Ratio | 1:88, providing high sensitivity for trace-gas detection | Automatic Background-Gas Injection |
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| Carrier-Gas Pressure Range | Up to 0.5 MPa; compatible with gas chromatographs in complex configurations | Reaction-Parameter Monitoring Accuracy | Reaction pressure: 1 Pa; reaction temperature: 0.01 °C |
| Gas-Circulation Parameters | |||
| Gas-Mixing Time | Less than 10 min for both H₂ and O₂ | Linearity | Calibration-curve linear regression coefficient R² > 0.999 |
| Repeatability | RSD < 2.5% for four consecutive injections at the same concentration | Magnetically Coupled Impeller Pump | No electrical wiring inside the system, eliminating hydrogen-explosion risks and interference from electrolytic hydrogen evolution. |
| Between-System Reproducibility | Deviation < 5%, supporting high data consistency | Reactor Types | Multiple reactor configurations for diverse application scenarios |
| Sampling Mode | Patented sampling valve manifold with a fully automatic online sampling module integrated into the system rather than the chromatograph | Circulation Piping | All circulation lines are made of borosilicate glass. The narrow-line inner diameter is 3 mm, avoiding small-bore chromatographic tubing and minimizing gas-flow resistance. |
| Other Parameters | |||
| Reactor |
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| Metal Protective Enclosure | Protects against damage to glass components, optical radiation, and potential reaction-gas leakage. | Light-Source Placement | Can be positioned in front of or behind the system to suit the laboratory-bench configuration. |
| Light Shield | Portable light shield effectively limits stray-light exposure. | Vacuum Pump | Compatible with multiple brands and models; pumping speed: 1 L/s; automatic start/stop during sampling; intermittent low-noise operation; one-way solenoid valve prevents pump-oil backflow. |
| Overall Dimensions | 500 (L) × 540 (W) × 780 (H) mm | ||
Operating Principle
The intelligent touchscreen control unit manages the sampling module. The system uses self-aspirating sampling, with a calibrated sample loop as the core metering component. A sampling line connected to the module is incorporated directly into the circulation loop. Before sampling, the module evacuates the sample loop to a high-vacuum state. The loop is then connected to the circulation line, allowing part of the sample gas to enter under the resulting pressure differential.
After sampling, the loop is isolated from the circulation line and connected to the gas chromatograph's carrier-gas line. The carrier gas sweeps the sample into the detector for analysis. Because the loop is subsequently filled with high-pressure carrier gas, it is evacuated again before the next sampling cycle to prevent carrier gas from entering the reaction system.
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