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The objective of this study is to make predictions concerning the persistence of 2,4,6-trinitrotoluene (TNT) and octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) in solid form both as individual explosive compounds and components of octol, and the resultant concentrations of explosives in water as a result of dissolution using three exploratory modeling approaches.
Parametric calculations are presented that confirm the importance of particle size and its variation as a result of dissolution.
NH4+ and PO43− are enriched due to ion exchange, and DSi is enriched either by ion exchange (as PO43−) or as a result of dissolution of biogenic silica.
Flow in a rock fracture is surprisingly sensitive to the evolution of flow paths that develop as a result of dissolution.
The purpose of the proposed models is to predict the solute concentration in the zone of the residual NAPL as a result of dissolution.
ZnCl2 was found to dissolve into NBR upon heating to a designed temperature, which was considered as a result of dissolution process induced by the occurrence of coordination reaction.
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At the late stages of crystallization, the open pores were closed as a result of dissolution-recrystallization of the newly synthesized CaCO3 particles.
Results of dissolution experiments can be analyzed in the same way.
The results obtained in the testing cell were compared with results of dissolution studies of mini-tablets coated in fluid bed apparatus.
Solid state characterization of S-SNEDDS by DSC and Powder XRD confirmed reduction in drug crystallinity which further supports the results of dissolution studies.
The results of dissolution experiments for benzene, toluene, m-xylene and naphthalene (BTXN) from a relatively insoluble oil phase (tridecane), residually trapped in a non-sorbing porous medium, are described.
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