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Dehydrogenation of ethylbenzene (EB) was examined in the presence of CO2, and the effect of CO2 on Fe2O3, Fe–Ce, Fe–K, and Fe–Ce–K oxide catalysts was evaluated. The rate equation was derived in relation to the Langmuir–Hinshelwood mechanism. The rate constant ( k) and the relative adsorption coefficient ( $$ Z_{{{\text{CO}}_{2} }} $$) were obtained, and it was found that addition of K in the catalyst increased both k and $$ Z_{{{\text{CO}}_{2} }}.$$ We found that CO2 had a strong affinity for the catalyst surface and that the active sites were basic. [ABSTRACT FROM AUTHOR]

A new physiological index (μ(PA)) is proposed to represent the autonomic nervous system (ANS) function. The index μ(PA) is defined as the natural logarithm of the ratio between two different frequency components of the pulsatile amplitude of the photoplethysmogram (PPG) signal. The discrimination ability and the reproducibility of μ(PA) have been compared with other traditional ANS indices. In the experiment, the electrocardiogram, the PPG and continuous blood pressure were measured in 59 healthy young subjects (age 25.7 ± 6.3) and 86 healthy elderly subjects (age 70.2 ± 4.1) at rest. The discrimination ability and the reproducibility were evaluated by Cohen's d between young and elderly groups and by the interclass correlation coefficient, respectively. The results showed that the elderly subjects were significantly (p<;0.001) lower than young subjects in μ(PA) and a few traditional indices introduced to be compared with μ(PA). Therefore, it suggests that μ(PA) is associated with the decrease in the ANS function accompanied by aging. Moreover, it showed that the discrimination ability and the reproducibility of the proposed index are comparable or larger than those of traditional indices. The proposed index based on the PPG signal will be applied to tele-healthcare systems for monitoring people's health in daily life in combination with the ratio of the standard deviation of the R-R intervals to their average value (CVRR).

3,3,4,4-Tetaaryldihydro[5]helicenes (1) and 1,1'-binaphthyl-2,2'-diylbis(diarylcarbenium)s (2(2+)) can be reversibly interconverted upon electron transfer, which is accompanied by a vivid color change (electrochromism) as well as by the formation/cleavage of a C-C bond ("dynamic redox behavior"). Because only the neutral donor 1 exhibits strong fluorescence, electrochemical input can further modify the fluorescent properties of the pair. Due to the configurational stability of the helicity in 1 and axial chirality in 2(2+), the redox reaction of optically pure material proceeds stereospecifically, which induces a chiroptical change such as circular dichroism (CD) as an additional output. The CD spectra of dications 2(2+) exhibit solvent dependency (chiro-solvatochromism), which is accompanied by solvatochromic behavior based on the pi-pi interaction of the two cationic chromophores as well as coordinative interaction of the Lewis basic solvent to the Lewis acidic triarylcarbenium moieties. Thus, the present system is endowed with multi-input functionality for modifying multiple output signals.