The transition stage is shortened by increasing the rate of polymerisation in the drops (either by increasing initiator concentration or using a higher reaction temperature).
Standard unmodified allele-specific primers may be more dependent upon using an optimized reaction temperature than the rhPCR method, so the experiments were repeated with anneal/extension temperatures ranging from 60°C to 70°C.
By using back-pressure regulator (BPR), a reaction temperature of 180 °C could be easily and readily achieved even in a low-boiling solvent [water/ethylene glycol EG)].
Catalytic measurements have been performed in CO2 reforming of CH4, using a fixed bed reactor at a reaction temperature ranging from 650 to 800 °C.
Meng et al. [70] were able to show the effect of feedstock quality on product distribution by investigating four types of feeds using a CEP-1 catalyst at a reaction temperature of 660 °C, residence time of 2.2 s, C/O weight ratio of 15.5 and steam-to-oil weight ratio of 0.75.
The beaker was maintained at a reaction temperature of 80°C using water bath.
The beaker was maintained at a reaction temperature of 80°C using a water bath for 30 min.
A presulfided NiMo/γAl2O3 catalyst and a reaction temperature of 325°C were used in all of the experiments.
The sand bath temperature was controlled at 5 10 °C above the reaction temperature using a temperature controller (Omega, HH501AJK), with consideration of heat loss and transfer.
AuNPs were also synthesized using different reaction temperature (0, 15, 28, 75, and 100 °C), different concentration of cell-free filtrate (× 0.5, × 1, × 2) and chloroaurate ions (0.5, 1, 2 mM).
