Examples of 'crystal modification' in a sentence

Meaning of "crystal modification"

crystal modification - This phrase refers to the process of altering or changing the properties of a crystal through various methods or techniques

How to use "crystal modification" in a sentence

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crystal modification
One crystal modification of dicyclanil is already known.
Surface morphologies obtained by crystal modification will now be described.
A crystal modification can be either a solvate or an ansolvate.
It is usually converted to the rutile crystal modification by calcining in a rotary kiln.
The crystal modification of ramatroban is employed in high purity in pharmaceutical formulations.
The obtained characteristic spectroscopic data are shown below for each crystal modification.
The isolation of this stable crystal modification IV was not straightforward.
Another problem related to ammonium nitrate is its transition from one crystal modification to another.
This gives crystal modification IV a more stable weight at varying relative humidity.
The melting point of cocoa butter depends on the crystal modification in which it exists.
This gives crystal modification IV advantageous properties with regard to bulk handling and formulation.
The seed crystals should be of crystal modification IV.
Characteristic for the crystal modification A is the thermogram in differential scanning calorimetry.
The crystalline Ciclosporin starting material may comprise Ciclosporin in any crystal modification.
In one aspect, the crystal modification is a monohydrate of elobixibat.

See also

In addition it is slightly hygroscopic, but no change in crystal modification is observed.
Figure 4 illustrates the crystal modification properties of the maleate copolymers of this invention.
It was thus a further challenge just to obtain XRPD-data for a pure crystal modification.
As a result, crystallization of primarily this crystal modification or only this crystal modification is achieved.
Crystal modification disrupts the crystalline structure of the scale, preventing scale formation.
Alternatively, the solubility of the active agent can be achieved by changing its crystal modification.
The a-type crystal modification can be prepared consistently by treating the toluene adduct with methanol.
The seed crystals may be selected according to quantity, size, habitus and crystal modification.
Also, during the drawing process, the less stable crystal modification can convert into a stable modification.
The crystal modification N of torasemide according to claim 1, characterized in that it is chemically pure.
X-ray analysis revealed the presence of the crystal modification A.
In a further embodiment, crystal modification D is formed during the preparation process of a formulation.
In a sixth aspect, the invention relates to crystal modification I of elobixibat.
The B-type crystal modification may also be obtained by heat-treating the toluene adduct under vacuum.
The X-ray diffraction pattern for this new crystal modification is shown in Figure 1.
The new crystal modification N is as defined in claim 1.
Figure 3 shows the X-ray diffraction pattern of the instant Y crystal modification.
Certain forms of elobixibat, such as crystal modification I of elobixibat, contain a non-stoichiometric amount of water.
Examples 1-3 relate to the production of a mixture of riboflavin crystals of crystal modification B and C.
Under milling the crystal modification ( monohydrate ) does not change.
FIG . 11 shows the DVS mass change plot for crystal modification IV.
This is clearly a different crystal modification than in the products of, for example, experiments 4a.
Figure 2 shows the X-ray diffraction pattern of the known B crystal modification.
It is an 1:1 salt and only one crystal modification has been observed.
FIG . 14 shows a plot of water uptake as a function of % RH for crystal modification I.
In a third aspect, the invention relates to crystal modification MeOH-1 of elobixibat.
FIG . 12A and 12B show a plot of water uptake as a function of % RH for crystal modification IV.
In a second aspect, the invention relates to crystal modification EtOH-1 of elobixibat.
FIG . 17 shows the high-resolution X-ray powder diffractograms of crystal modification I and crystal modification IV.
In a fourth aspect, the invention relates to crystal modification 1-PrOH-1 of elobixibat.
In a fifth aspect, the invention relates to crystal modification 2-PrOH-1 of elobixibat.

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