11 research outputs found
Mechanistic Study of Oil/Brine/Solid Interfacial Behaviors during Low-Salinity Waterflooding Using Visual and Quantitative Methods
Despite the many
studies of low-salinity waterflooding (LSWF),
its underlying mechanisms are not well understood as a result of the
complexity of the oil/brine/solid interfacial behaviors. Moreover,
the widely held belief that LSWF is effective only under certain conditions
has not been conclusively proven. Therefore, the static and dynamic
interfacial behaviors during LSWF were visually and quantitatively
studied in this work to elucidate the underlying mechanism(s). The
results showed that LSWF effectively promotes oil recovery by causing
double-layer expansion (DLE) and hydrocarbon solubilization. The DLE resulted from multicomponent
ion exchange (MIE), as revealed by contact angle, ζ potential,
and conductivity measurements. Emulsions prepared with low-salinity
brines (≤0.21 wt %) were noticeably heavier and quite stable,
demonstrating the significant solubilization effect of LSWF. The oil
displacement dynamics observed in a visual micromodel indicated that
LSWF increased the oil recovery factor by 4% (secondary) and 1.7%
(tertiary) in water–wet porous media, whereas in oil-wet porous
media, LSWF was even more efficient than high-salinity waterflooding
(HSWF) when employed as the secondary mode. Moreover, the macroscopic
sweep and microscopic displacement efficiencies were quantitatively
determined using an image analysis technique to verify the proposed
mechanisms
The Potential of a Novel Nanofluid in Enhancing Oil Recovery
A surface-active
and “green” flooding agent, modified
nanocellulose (NC), which is expected to be an alternative to the
current flooding systems for enhancing oil recovery (EOR), was provided
in this work. The physical properties of the NC samples including
dispersity, rheology, phase behavior, emulsifiability, etc., as a
function of mass fraction and charge density, were comprehensively
studied to evaluate their EOR potential. The results indicate that
this modified nanomaterial could be well dispersed in 1 wt % NaCl
brine, forming a series of homogeneous nanofluids at the concentration
above 0.4 wt %. Rheological analysis evidenced the viscoelastic properties
and pronounced shear-thinning behavior of the nanofluids. Because
of the presence of the active groups, the dynamic interfacial tension
(Oil/Nanofluid) decreased to an order of 10<sup>–1</sup>mN/m,
which accordingly promotes the microscopic recovery efficiency through
an emulsification effect. It was also observed that the emulsifiability
of the nanofluids was closely related to the charge density. Visual
EOR experiments were conducted in a micromodel, from which two mechanisms,
(1) sweep volume improvement and (2) emulsification and entrainment,
were established for NC nanofluid flooding. As an eco-friendly material,
this nanofluid is supposed to be a promising flooding agent in the
near future
Prognostic value of plasma EGFR ctDNA in NSCLC patients treated with EGFR-TKIs
<div><p>Objective</p><p>Epidermal growth factor receptor (EGFR) specific mutations have been known to improve survival of patients with non-small-cell lung carcinoma (NSCLC). However, whether there are any changes of EGFR mutations after targeted therapy and its clinical significance is unclear. This study was to identify the status of EGFR mutations after targeted therapy and predict the prognostic significance for NSCLC patients.</p><p>Methods</p><p>A total of forty-five (45) NSCLC patients who received EGFR-TKI therapy were enrolled. We identified the changes of EGFR mutations in plasma ctDNA by Amplification Refractory Mutation System (ARMS) PCR technology.</p><p>Results</p><p>In the 45 cases of NSCLC with EGFR mutations, the EGFR mutation status changed in 26 cases, in which, 12 cases (26.7%) from positive to negative, and 14 cases (31.1%) from T790M mutation negative to positive after TKI targeted therapy. The T790M occurance group had a shorter Progression -Free-Survival (PFS) than the groups of EGFR mutation undetected and EGFR mutation turned out to have no change after EGFR-TKI therapy (p < 0.05).</p><p>Conclusions</p><p>According to this study, it’s necessary to closely monitor EGFR mutations during follow-up to predict the prognosis of NSCLC patients who are to receive the TKI targeted therapy.</p></div
Influence of Individual Ions on Oil/Brine/Rock Interfacial Interactions and Oil–Water Flow Behaviors in Porous Media
The low salinity
effect (LSE) in enhanced oil recovery (EOR) is
widely accepted. However, its underlying mechanisms remain unclear
due in part to the complex interactions at the oil/brine/rock interface.
The chemistry of brine largely depends on the ionic composition. Thus,
in this work, attention was placed on the roles of individual ions
and salinity in LSE through direct measurements of oil/brine/rock
interfacial behaviors, oil displacement efficiencies, and oil–water
relative permeability in sandstone porous media. The results showed
that the oil/water interfacial tensions (IFTs) were weakly dependent
on ion and the lowest IFTs were generated at the salinities of 0.2–0.5
wt %. In contrast, the interfacial dilational modulus varied significantly
with ion types and salinities due to the adsorption of polar components
at the oil/water interface. Moreover, wettability alteration of the
sandstone surface was found to be associated with the divalent ions
in our work. As a result of the viscoelastic interfaces, the breakage
of oil column into oil droplets or ganglia was delayed, which subsequently
led to the improvement of the oil–water relative permeability
and oil displacement efficiencies. Based on the analysis, it was concluded
that HCO<sub>3</sub><sup>–</sup>, Mg<sup>2+</sup>, and SO<sub>4</sub><sup>2–</sup> were potential-determining ions (PDIs)
in LSE. The results of the tests, to our knowledge, are the first
that particularly emphasize the roles of individual ions at the interfaces
and oil–water flow patterns in porous media
A Scalable “Junction Substrate” to Engineer Robust DNA Circuits
Versatile building blocks are essential
for building complex and
scaled-up DNA circuits. In this study, we propose a conceptually new
scalable architecture called a “junction substrate”
(J-substrate) that is linked by prepurified double-stranded DNA molecules.
As a proof-of-concept, this novel type of substrate has been utilized
to build multi-input DNA circuits, offering several advantages over
the conventional substrate (referred to as a “linear substrate”,
L-substrate). First, the J-substrate does not require long DNA strands,
thus avoiding significant synthetic errors and costs. Second, the
traditional PAGE purification method is technically facilitated to
obtain high-purity substrates, whereby the initial leakage is effectively
eliminated. Third, the asymptotic leakage is eliminated by introducing
the “junction”. Finally, circuits with the optimized
J-substrate architecture exhibit fast kinetics. We believe that the
proposed architecture constitutes a sophisticated chassis for constructing
complex circuits