Sentence examples for tension was determined by from inspiring English sources

Bubble areas and volumes were calculated by an original algorithm relating bubble height and diameter to areas of revolution, and bubble surface tension was determined by the method of Malcolm and Elliot [70].

The surface tension was determined by analyzing the shape of the droplet using standard procedures.

Before performing the hip reduction, the hip adductor tension was determined by abducing the hip joint.

The Whole Body Tension was determined by dividing the average of the top 5 or top 10 forward pulling tensions, respectively, by the body weight.

The reduction of surface tension was determined by comparing the surface tension of the noninoculated medium (65.66 ± 4 mN/m) with the cell-free medium obtained after the incubation of tested bacteria.

Excess surface tension is determined by the following equation [28]: sigma^{text{E}} = sigma - (x_{1} sigma_{1} + (1 - x_{1} )sigma_{2} ), (14 where σ E is excess surface tension in mN m−1.

Works of adhesion and spreading that are dependent on the contact angle of water droplet on solid surfaces and water total surface tension were determined by Eqs. 7 and 8, respectively [17]: W_{a} = gamma_{l}^{text{tot}} left( {cos theta + 1} right), (7) W_{S} = gamma_{l}^{text{tot}} left( {cos theta - 1} right).

The results support the experimental observations that initially the surface tension is determined by a combination of adsorption from the liquid and the vapor phase, whereas at the final steady-state the surface tension is determined primarily by adsorption from the vapor phase.

Usually, tissue oxygen tension is determined by the balance between the blood flow and tissue oxygen consumption.

From the inner diameter d of the injection tube (d = 250 µm), the surface tension is determined by mg/(π*d*f) where f is a Wilkinson geometric parameter correction that depends on the ratio between d and the radius of the detached drop and g is the gravity constant.

The chondrogenic differentiation potential of inner 2/3rd and outer 1/3rd human MFCs cultured in collagen type I scaffolds for 21 days under normal (21%) or low (3%) oxygen tension was determined at the molecular level by comparing gene expression of monolayer cells immediately prior to cell seeding (P3) with scaffold constructs at the end of chondrogenic culture (D21).