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Relationship between inspired and expired gas temperatures in a hyperbaric environment.

When breathing room air at sea level the expired gas temperature (TE) increases in proportion to the inspired one (TI). Previous studies conducted under hyperbaric conditions have assumed that the TE vs TI relationship was the same when humans breathed room air at atmospheric pressure or helium-oxygen mixture under hyperbaric conditions. We hypothesized that the use of dilutant gases, as helium (He) or hydrogen (H2), having low density but high specific heat compared to nitrogen, could change the TE vs TI regression. The present study was conducted on 3 professional divers participating in the COMEX Hydra IX experiment. Three conditions were studied: A, (23.5 ATA, He-H2-O2 mixture); B, (21 ATA, H2-O2 mixture); and C, (21 ATA, He-O2 mixture). In each condition six different inspired temperatures were tested, while minute ventilation, TI and TE values were measured simultaneously. In all cases a linear relationship was found between TE and TI, but the slopes of the regression lines obtained in conditions A and B (gas mixture containing H2) were significantly lower than in condition C (He-O2 mixture). Computation of the convective respiratory heat loss (Cr) revealed that, when the subjects breathed the coldest gas mixtures (+10 degrees C), Cr value was 1.6 times higher in condition B than in C. These data are consistent with theoretical considerations and they demonstrate that a single equation cannot be used to predict the TE vs TI relationship in all environmental circumstances.

Body Temperature Regulation↗

Evaluation of the reaction kinetics of CORTOSS, a thermoset cortical bone void filler.

The primary objective of this research is to evaluate the reaction kinetics of CORTOSS(TM), a thermoset, Bis-GMA (2,2-bis[4-(2-hydroxymethacryloxypropyl) phenyl]propane) composite system as a function of time, material storage temperature and the temperature of the surrounding environment (site temperature). This study utilizes probability theory to predict the percentage of bifunctional monomers with 0,1 and 2 functional groups that have been reacted. This is a strong indicator of the potential for leaching unreacted components. A differential scanning calorimeter (DSC) was used to measure the isothermal enthalpy at varying site temperatures. After isothermal monitoring, the samples were dynamically heated from the respective isothermal temperature to 175 degrees C at 15 degrees C/min to measure the residual enthalpy from the unreacted functional groups. The experimental results indicate that the degree of conversion for this bifunctional system ranged from 76% to 86%. Applying probability theory it has been determined that approximately 95% of the bifunctional monomers are present with at least one double bond reacted and up to 5% of monomers remain unreacted. This is consistent with theoretical values postulated for various diffusion controlled thermoset systems (Macromolecules 32 (1999) 3913). Overall, curing under physiological conditions yielded a faster reaction rate and a significantly higher degree of conversion as compared to the lower site temperature conditions.

Benzeneacetamides↗