Multivariable analysis was used to explain bacteriological cure as a function of sex, age, initial body weight, history of previous treatment and the region of report.
A logistic regression model was built to analyse cure as a function of sex, age, initial body weight, previous treatment history, and the region where the patient was treated.
Open image in new window Fig. 2 Dependence of the conversion rate of polymeric systems curing time at different isothermal temperatures (the A series) and isothermal reaction rate of the polymeric systems curing as a function of conversion at different isothermal temperatures (the B series).
The adhesion properties of the room temperature cured films as a function of alkoxysilane concentration were evaluated.
Curing energetics as a function of alkyne type, investigated through a dynamic differential scanning calorimetry approach, showed a distinct divide between the averaged activation energies of the propiolate and propargyl-type crosslinkers, 69.2 73.6 kJ/mol versus 82.3 86.4 kJ/mol, respectively.
Measured friction coefficients were maximum at the start of the cure cycle and varied as a function of degree of cure and ramp rate owing to change in the tool part interface, cure shrinkage, resin/composite properties, residual stress, and mode of interface failure.
This approach allows an evaluation of cure chemistry and kinetics as a function of temperature, resin constituents, or catalyst addition.
The initial intensity of charge recombination luminescence (CRL) emitted by epoxy resins after brief periods of UV irradiation during cure has been measured for a number of resins as a function of cure time.
The fluorescence spectrum of 1- 4-dimethylaminophenyl -6-phenyl-1,3,5-hexatriene (DMA-DPH) dissolved in a stoichiometric mixture of diglycidyl ether of bisphenol A and diethylene triamine was measured as a function of cure time at various cure temperatures.
Ultrahigh strain rate performance in a series of model amine cured epoxy resins was investigated as a function of the glass transition temperature (Tg) of the cured polymer network, where the network Tg was systematically varied through the monomer stiffness, structure, and size.
Heat generation term, expressed as a function of cure rate and the total heat generation due to cure reaction, is introduced to account for the effect of heat liberated during the process.
