3 research outputs found
Effect of Solution Silicate on the Precipitation of Barium Sulfate
The presence of silicate during barium sulfate crystallization
has different impacts depending on the pH of the solution. At pH 7
the dominance of the protonated form (H<sub>4</sub>SiO<sub>4</sub>) and possible polymerization of the silicate impacts mainly on the
aggregation state and on twinning of the barium sulfate formed. At
higher pH values (∼10), the silicate ion present is able to
influence both morphology and partially substitute for sulfate in
the lattice. Interesting fibrous particles are formed under these
conditions, but this is not due to mesocrystal formation as the particles
are observed to be single crystalline in nature. These fibrous sections
are found to be dominant on the surface and are highly porous. These
particles are different, however, to the biomorphs formed when crystallization
of barium carbonate occurs in the presence of silicate. This is because
the speciation of sulfate does not change over a large pH range. The
impact of silicate on barium sulfate particles is similar to the impact
on calcium carbonate and strontium sulfate crystallization
The Impact of Sugars on Kidney Stone Formation
Various studies have found a trend connecting diabetes
mellitus
or carbohydrate malabsorption syndromes to kidney stone formation.
However, the underlying mechanism causing this impact is unclear.
This study aimed to investigate whether some of this correlation is
due to the underlying chemistry of sugars as crystal growth modifiers.
Thus, the impact of major dietary monosaccharides (glucose, fructose,
and galactose) and disaccharides (lactose and sucrose) on the formation
of calcium oxalate was investigated from a crystallization perspective.
The nucleation rate of calcium oxalate generally showed a promotion
when monosaccharides were present. An analysis of the crystals with
Raman spectroscopy found that signals for the monosaccharides are
present within the crystal, showing an association between the sugars
and calcium oxalate. When lactose was present, there was an obvious
promotion of nucleation. When sucrose was present, an interaction
with both the crystal and the solution ions was observed. The presence
of galactose had the most influence on the zeta potential of calcium
oxalate when zinc ions were present, resulting in the smallest zeta
potential value. These results suggest that the sugars in urine may
promote calcium oxalate formation and agglomeration, and this may
suggest a chemical connection to the higher prevalence of stones in
diabetic patients
CO<sub>2</sub> and CH<sub>4</sub> Wettabilities of Organic-Rich Shale
CO<sub>2</sub> and
CH<sub>4</sub> wettabilities of organic-rich
shale are important physicochemical parameters that significantly
influence CO<sub>2</sub> sequestration and CH<sub>4</sub> production.
However, there is a serious lack of understanding of these aspects
because the data available are scarce. Thus, we evaluated organic-rich
shale CO<sub>2</sub> and CH<sub>4</sub> wettabilities (i.e., brine/shale/gas
systems) through advancing and receding brine contact angle measurements
as a function of pressure, temperature, salinity, and ion type (as
these can vary significantly in underground formations). The results
indicated that the brine contact angles for both CO<sub>2</sub>/CH<sub>4</sub>–brine–shale systems increased with pressure
and salinity, but decreased with temperature. However, these effects
were much less significant for CH<sub>4</sub>. Furthermore, the brine
contact angles for the CO<sub>2</sub>–brine–shale system
reached 180° (i.e., the shale was completely wetted by CO<sub>2</sub>) when the pressure reached 30 MPa at 343 K and ∼9
MPa at 298 K. The brine contact angles for the analogue CH<sub>4</sub> systems was much lower (50°–90°), only indicating
weakly water-wet to intermediate-wet conditions. Finally, the brine
contact angles for CO<sub>2</sub>–brine–shale system
were also larger for divalent ions (Ca<sup>2+</sup>, Mg<sup>2+</sup>) than for monovalent ions (Na<sup>+</sup>, K<sup>+</sup>), while
ion type had no significant influence on CH<sub>4</sub> wettability.
However, a similar CO<sub>2</sub>/CH<sub>4</sub> density resulted
in a similar wettability. Consequently CH<sub>4</sub> could not be
used as a proxy for predicting CO<sub>2</sub> storage capacities,
unless they have similar densities