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JKSPE : Journal of the Korean Society for Precision Engineering

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"장입량"

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"장입량"

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A study investigated hydrogen permeability in sulfur-cured NBR composites filled with carbon black (CB) and silica, using volumetric analysis across pressures ranging from 1.2 to 92.6 MPa. Both pure NBR and MT CB- and silica-filled NBR exhibited a single sorption mechanism that followed Henry’s law, indicating hydrogen absorption into the polymer chains. In contrast, HAF CB-filled NBR displayed dual sorption behavior, adhering to both Henry’s law and the Langmuir model, which suggests additional hydrogen adsorption at the filler interface. Hydrogen diffusivity in NBR followed Knudsen diffusion at low pressures and bulk diffusion at high pressures. In HAF CB-filled NBR, permeability decreased exponentially with increasing density, while in MT CB- and silica-filled NBR, it declined linearly. The strong polymer-filler interactions in HAF CB significantly influenced permeability. Permeability trends closely correlated with hardness, tensile strength, and density, allowing for the establishment of quantitative relationships between these physical and mechanical properties. These findings indicate that analyzing these properties can predict hydrogen permeability, positioning NBR composites as promising sealing materials for high-pressure hydrogen storage in refueling stations and fuel cell vehicles.

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Hydrogen gas sensors are essential for industrial safety, environmental monitoring, and the energy sector. As hydrogen infrastructure expands and hydrogen fuel cell vehicles become more widespread, precise detection of hydrogen, which has a wide explosive range, has become increasingly critical. To ensure accurate detection of hydrogen in real-world conditions, sensor technologies must offer high sensitivity, stability, and reproducibility, along with cost-effectiveness, fast response time, and compact design. This study introduces a hydrogen gas sensor based on pressure analysis principles. This sensor was developed to quantitatively evaluate hydrogen uptake, diffusion behavior, solubility, and release characteristics in polymers under high-pressure conditions. Experimental results demonstrated the sensor’s excellent performance, with a stability of 0.2%, a resolution of 0.12 wt·ppm, and a measurement range of 0.12 to 1500 wt·ppm, all within 1 second. Furthermore, the sensor's sensitivity, resolution, and detection range could be tuned to suit different operational environments. Uncertainty analysis showed an expanded uncertainty of 8.8%, confirming the system’s capability for real-time hydrogen detection and characterization. This sensor technology is well-suited for applications in hydrogen refueling stations and fuel cell systems, contributing to the advancement of a safe hydrogen society.
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Gas sensors are crucial devices in various fields such as industrial safety, environmental monitoring, and gas infrastructure. Designed to have high-sensitivity, stability, and reliability, gas sensors are often required to be cost-effective with quick response and compactness. To meet diverse needs, we developed two types of gas sensors based on volumetric and manometric analyses. These sensors could operate by measuring gas volume and pressure changes, respectively, based on emitted gas. These sensors are capable of determining gas transport parameters such as gas uptake, solubility, and diffusivity for gas-charged polymers in a high-pressure environment. These sensors can provide rapid responses within one-second. They can measure gas concentration ranging from 0.01 wt·ppm to 1,500 wt·ppm with adjustable sensitivity and measurement ranges. As a result, such sensor system can be used to facilitate real time detection and analysis of gas transport properties in pure gases including H₂, He, N₂, O₂, and Ar.
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