STUDY ON BEHAVIOR OF TRAPPED HYDROGEN IN 18Ni MARAGING STEEL BY THERMAL HYDROGEN EVOLUTION TECHNIQUE

The interaction of hydrogen with interface between the precipitates and the martensitie matrix in 18Ni maraging steel has been studied by means of thermal evolution hydrogen technique us- ing gas chromatograph as hydrogen detector.An evolution rate peak has been observed at 451 K.The height of the peak relates to the amount and distribution of the precipitates.The activation energy for hydrogen escaping from the trap sites is 23.2 kJ/mol.

Structure evolution of oxygen removal from porous carbon for optimizing supercapacitor performance

The presence of oxygen functional groups is detrimental to the capacitive performance of porous carbon electrode in organic electrolyte. In this regards, hydrogen thermal reduction has been demonstrated effective approach in removing the unstable surface oxygen while maintaining the high porosity of carbon matrix. However, the exact evolution mechanism of various oxygen species during this process, as well as the correlation with electrochemical properties, is still under development. Herein, biomass-based porous carbon is adopted as the model material to trace its structure evolution of oxygen removal under hydrogen thermal reduction process with the temperature range of 400–800 °C. The optimum microstructure with low oxygen content of 0.90% and proper pore size distribution was achieved at 700°C. XPS, TPRMS and Boehm titration results indicate that the oxygen elimination undergoes three distinctive stages(intermolecular dehydration, hydrogenation and decomposition reactions). The optimum microstructure with low oxygen content of 0.90% and proper pore size distribution was achieved at 700 °C. Benefiting from the stable electrochemical interface and the optimized porous structure, the as-obtained HAC-700 exhibit significantly suppressed self-discharge and leak current, with improved cycling stability, which is attributable to the stabilization of electrochemical interface between carbon surface and electrolyte. The result provides insights for rational design of surface chemistry for high-performance carbon electrode towards advanced energy storage.

Hot deformation behavior of a near alpha titanium alloy with/without thermal hydrogen processing

The true stress-true strain curves of Ti-6Al-2Zr-IMO-IV alloy with hydrogen were obtained by hot compression test. The microstructures of the alloy before and after thermo-compression were observed. The apparent activation energies of deformation were calculated for the alloy with and without hydrogen. The behavior and mechanism of deformation for hydrogenated Ti-6A1-2Zr-IMO-IV alloy at high temperature were analyzed. The relationship between hydrogenation time and hydrogen content at 800 ℃ can be expressed as the equation： CH（t）=1.2-1.2exp（-t/120）. The true stress-true strain curves of hot compression for Ti-6Al-2Zr-IMO-IV alloy with hydrogen first move down and then move up as hydrogen content increases. Appropriate hydrogen content can reduce the peak of flow stress to minimal value. The apparent activation energies of deformation of the alloy with 0.47% hydrogen content and without hydrogen were calculated as 140 kJ·mol^-1 and 390 kJ-mol^-1, respectively, at 800 ℃ and at strain rate 8.3×10^4 s^-1. The apparent activation energy of deformation increases when the strain rate enhances from 8.3×10^-4 s^-1 to 8.3×10^-2 s^-1.

Thermal,physical and mechanical properties of hydrogenated dimer acid-based Nylon 636/Nylon 66 copolymers

Hydrogenated dimer acid-based Nylon 636/Nylon 66 copolymers were synthesized by in situ polymerization. The effects of Nylon 66 contents on the copolymers were characterized by intrinsic viscosity measurements, attenuated total reflection-Fourier transform infrared spectroscopy, X-ray diffraction, differential scanning calorimetry, thermogravimetric analysis and mechanical tests. The results showed that incorporation of Nylon 66 into hydrogenated dimer acid-based Nylon had no significant effect on the glass transition or melting temperatures. However, the crystallization temperature, crystallinity degree and the maximum rate of decomposition temperature from derivative thermogravimetry measurements vary. Mechanical testing data revealed that with increasing Nylon 66 concentrations, the tensile strength of copolymers increased, while the elongation at break point and notched izod impact strength decreased. The physical and mechanical properties of HN-40, HN-50 and HN-60 are similar to those of the current PAl 1, PAl212, and PAlll 1 Nylon products.