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It is molecular orientation of matrix that determines the tensile properties of oriented blends.
By tweaking the size and orientation of matrix pores, researchers attempted to emulate variations of cellular structure and function in a real cortex.
There seems to be a marked correlation of relief type with the surface orientation of matrix grains.
The orientation of matrix cracking was analyzed, based on surface observations, and its connection to the macroscopic stress strain response provides important insight into the underlying deformation mechanisms.
As for the oriented blends, however, the presence of dispersed phase in the blends, independent of phase morphology and crystallinity, always makes tensile properties to be deteriorated through reducing molecular orientation of matrix.
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Changes in the orientation of the matrix, and in matrix eccentricity and size, within the first four generations followed by stability after generation 4 for uranium suggest that in this novel environment epigenetic or acclimation effects may have caused changes in the P-matrix.
The effect of orientation hardening of matrix polymers on the toughness of polymer blends was examined.
The modified process called rapid CVI (r-CVI) allows a fast production of the matrix as well as the adjustment of graphene orientation of the matrix.
The difference between the first eigenvector of two matrices explains most of the variation in the orientation of the matrix [ 15, 61].
It was demonstrated that a Ti11Ni14 precipitate grown from a supersaturated cubic TiNi matrix has a lens-like shape, with its normal parallel to the [111]B2 orientation of the matrix, in agreement with experimental observations.
This alignment occurs because the fibers experiencing the greatest amplitudes of stretch (i.e. the orientation of large matrix normal strain) disassemble relatively quickly, leading to the accumulation of fibers in the direction of smallest matrix normal strain.
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