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The flow and transport of polymer solutions through porous media are ubiquitous in myriad scientific and engineering applications. With escalating interest in adaptive polymers, understanding the flow dynamics of their solutions is indispensable (yet lacking). Here, the hydrophobic-effect-driven reversible associations in a self-adaptive polymer (SAP) solution and its flow characteristics in a microfluidic-based "rock-on-a-chip" device have been analyzed. The hydrophobic aggregates were fluorescent labeled; this enabled a direct visualization of the in situ association/disassociation of the polymer supramolecular assemblies in pore spaces and throats. Furthermore, the influence of this adaptation on the macroscopic flow behavior of the SAP solution was analyzed by comparing its flow with that of two partially-hydrolyzed polyacrylamide (the molecular weight (MW)-equivalent HPAM-1 and ultrahigh-MW HPAM-2) solutions in the semi-dilute regime with similar initial viscosities. At low flow rates (with shear predominance), the SAP solution showed a low shear viscosity compared to HPAM-1, indicating a higher shear susceptibility for association than chain entanglement. Although the SAP exhibited the same elastic instability as the non-adaptive polymers above a threshold flow rate, the adaptable structure of the former advanced the onset of its viscoelastic-governed flow, providing a stronger flow resistance, possibly through an extension resistance. Furthermore, 3D-media analysis indicated that the reversible association/disassociation of SAP increased the accessible pore space during nonaqueous-liquid displacement, facilitating oil production.
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A unique experiment design is proposed to study the asphaltene precipitation caused by multiple contact processes during gas injection. The newly proposed experiment quantified the asphaltene precipitation at different methane contact steps. Twenty times methane contacts and corresponding asphaltene precipitation states are measured using a light scattering setup under reservoir condition. The amount of the asphaltene precipitation, the composition changes, and the physical properties changes are measured for the 20 times methane contacts. After verifying the asphaltene precipitation in the static experiments, the formation damage caused by the asphaltene precipitation is studied by core flooding tests for three different permeability cases. We found that the primary asphaltene precipitation mechanism in the multiple contact process during methane injection is not the composition change caused by methane extraction. The methane-induced asphaltene stability loss during the multiple contact process is vital. The size and the structure of asphaltene precipitation particles in the crude oil change with the methane contacts. We found that the mechanism of permeability reduction caused by asphaltene precipitation is different depending on the porous media pore throat size and the asphaltene precipitation particle size. Under our experimental condition, the asphaltene precipitation acts as a conformance control method, leading to well-distance optimization considerations in field applications.
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HYPOTHESIS: The CO2-sensitive dispersion/precipitation transition of polymer latexes fabricated based on a responsive emulsifier is a promising way to conveniently acquire bulk polymer materials. Nevertheless, the tedious synthesis procedures for switchable surfactants and the harsh operating requirements for the sensitive latexes constrain the applicability of the approach for latex preparation. Therefore, a new strategy for generating latexes with tunable CO2 responsiveness in a maneuverable way is urgently needed. EXPERIMENTS: In this work, a CO2-switchable electrostatic interaction is introduced to construct responsive latexes. A series of lightly crosslinked poly(diethylaminoethyl methacrylate-styrene) [P(DEA-St)] latexes with different PDEA contents were fabricated via one-pot emulsion copolymerization, with divinylbenzene and sodium dodecylsulfate (SDS) used as the crosslinker and anionic emulsifier, respectively. The influence of the DEA feeding ratio on the resulting P(DEA-St) colloids was characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. Then, a cyclic CO2/N2 input was introduced to verify the response transitions of polymer latexes. FINDINGS: Accompanied by the stepwise decrease of DEA feeding ratio, the morphology of the resulting copolymerized nanoparticles changed from an ambiguous bulge to the typical spherical pattern. In addition, the P(DEA-St) latexes treated by cyclic CO2/N2 exhibit four different types of response modes, namely (i) CO2-switchable swelling/deswelling transition, (ii) CO2-reversible dispersion/coagulation transition, (iii) CO2-induced irreversible destabilisation and (iv) CO2-insensitive latexes. The CO2-responsive destabilisation is highly applicable in the separation and transportation fields of commercial latex products, such as poly(methyl methacrylate), poly(n-butyl acrylate) and poly(butyl methacrylate) colloids.
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The synthetic water-soluble polymer, partially hydrolyzed polyacrylamide (HPAM), has been most widely used for enhanced oil recovery (EOR); however, its poor thermal stability and weak salt tolerance impede further application in high-temperature and high-salinity oil reservoirs. To address such deficiencies, three polysaccharides, xanthan gum, diutan gum, and scleroglucan, were examined in comparison with HPAM on rheological behaviors, shearing resistance, long-term thermal stability, and core flooding test. It was found that all of these three polysaccharides were less sensitive to salinity and shearing time, while HPAM showed a monotonous decrease in viscosity with increasing monovalent cations and shearing history. After 90 days of aging at 85 °C and 10.1 × 104 mg·L-1 of total dissolved solids with 1.0 × 103 mg·L-1 of Ca2+, the viscosity of diutan gum and scleroglucan solutions nearly remained unchanged; on the contrary, the viscosity of xanthan gum and HPAM solutions drops massively. Core flooding tests at 85 °C with the same initial viscosity demonstrated that all polymers showed good transportation in porous media, and 16, 13, and 11% of oil recovery were obtained by diutan gum, scleroglucan, and xanthan gum, respectively, while only 10% was obtained from HPAM. These comparative results may underpin the potential of diutan gum and scleroglucan to be used in the EOR process in HTHS oil reservoirs.
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AIMS: Cigarette smoking results in well-known negative reproductive consequences. However, the role of histone deacetylase 1 and 2 (HDAC1/2) in the structural changes of uterine tissues induced by cigarette smoke (CS) exposure and the therapeutic potential of trichostatin A (TSA), a HDAC inhibitor, have not been investigated. MAIN METHODS: Female mice were exposed to CS twice daily for 30â¯days and TSA was injected intraperitoneally into CS-exposed mice on alternate days in the TSA-treated group. Uteri in the estrus phase were weighed and uterine histomorphology and HDAC1 cell distribution were examined by HE and immunohistochemistry. Markers associated with macro-autophagy (Beclin-1), autophagic flux (increased LC3-II and a lack of p62 accumulation), autophagy inhibiting factor (mTOR, phosphorylated mTOR and its upstream IRS, phosphorylated IRS), HDAC1/2, FOXO1 and FOXO3 were assessed by Western blot. KEY FINDINGS: CS exposure decreased body weight and triggered uterine histomorphologic alterations, including a thinner myometrium and a reduced number of glandular and interstitial cells. HDAC1/2 were activated in uterine tissues after CS exposure and TSA effectively inhibited HDAC1/2 activation and attenuated the loss of body weight and uterine wet weight induced by CS exposure. TSA effectively restored the thickness of the myometrium and number of glandular and interstitial cells. TSA also restored the expression of markers of macro-autophagy (LC3-II and Beclin-1) and reduced phosphorylated mTOR, phosphorylated IRS, FOXO1 and FOXO3 activation. SIGNIFICANCE: TSA inhibited uterine histomorphologic alterations induced by CS exposure. The TSA effect might be associated with resumption of macro-autophagy via HDAC1/2 inhibition.