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In this paper the deformation and failure behaviour of soft synthetic detergent granules is investigated experimentally using single granule and bulk compression analyses.
On the basis of 1 molar = 6.0221367 × 1023 molecules, 415 molecules of PC1/3, 1677 molecules of PC2, and 1188 molecules of CPE were computed per single granule of each single islet cell as a rough approximation.
The breakage behaviour of wet granules produced in a high-shear mixer was investigated experimentally using single granule impact tests and the results are described in terms of the critical impact velocity, breakage pattern, and extent of breakage.
This paper reviews the study of breakage from the process scale down to the single granule and sub-granule scale, discussing largely experimental results complemented with some modelling results.
The drying behaviour of one single granule, a porous particle, can be described using the continuum approach, the pore network modelling method and the shrinkage of the diameter of the wet core approach.
In order to facilitate the design process, mathematical expressions have been provided showing the relationships among the area of single granule, the number of the external connections, the area of the reconfiguration multiplexers and the probability of failure of the system.
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It is shown that the ratio of the yield pressure of single granules to the Heckel parameter for this type of granules is less than one, and is about 0.5.
Furthermore, the bulk compression of soft spheres, with the properties, which are the same as those of single granules used here, is simulated by distinct element method (DEM) and the predictions are compared with the experimental results.
A novel triaxial apparatus employing overlapping rigid boundaries has been designed and constructed for experimental measurement of contact forces under confined compression of single granules in the mm-scale.
Instead, the distribution of β-actin mRNA granules within the cells was altered, since single granules appeared to form "clusters" distributed within the cell cytoplasm (Figure 9A inset).
The advantage of this method is that it can follow peptide secretion on a rapid timescale and can detect release from single granules [22], [23].
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