Improving Oil Recovery of the Heterogeneous Low Permeability Reservoirs by Combination of Polymer Hydrolysis Polyacrylamide and Two Highly Biosurfactant-Producing Bacteria

Polymer hydrolysis polyacrylamide and microbes have been used to enhance oil recovery in many oil reservoirs. However, the application of this two-method combination was less investigated, especially in low permeability reservoirs. In this work, two bacteria, a rhamnolipid-producing Pseudomonas aeruginosa 8D and a lipopeptide-producing Bacillus subtilis S4, were used together with hydrolysis poly-acrylamide in a low permeability heterogeneous core physical model. The results showed that when the two bacterial fermentation liquids were used at a ratio by volumeof 1:3 (v:v), the mixture showed the optimal physicochemical properties for oil-displacement. In addition, the mixture was stable under the conditions of various temperature (20–70 °C) and salinity (0–22%). When the polymer and bacteria were mixed together, it had no significant effects in the viscosity of polymer hydrolysis polyacrylamide and the viability of bacteria. The core oil-displacement test displayed that polymer hydrolysis polyacrylamide addition followed by the bacterial mixture injection could significantly enhance oil recovery. The recovery rate was increased by 15.01% and 10.03%, respectively, compared with the sole polymer hydrolysis polyacrylamide flooding and microbial flooding. Taken together, these results suggest that the strategy of polymer hydrolysis poly-acrylamide addition followed by microbial flooding is beneficial for improving oil recovery in heterogeneous low permeability reservoirs.

Polymer-Conjugated Carbon Nanotubes for Biomolecule Loading

Nanomaterials have emerged as an invaluable tool for the delivery of biomolecules such as DNA and RNA, with various applications in genetic engineering and post-transcriptional genetic manipulation. Alongside this development, there has been an increasing use of polymer-based techniques, such as polyethyleneimine (PEI), to electrostatically load polynucleotide cargoes onto nanomaterial carriers. However, there remains a need to assess nanomaterial properties, conjugation conditions, and biocompatibility of these nanomaterial-polymer constructs, particularly for use in plant systems. In this work, we develop mechanisms to optimize DNA loading on single-walled carbon nanotubes (SWNTs) with a library of polymer-SWNT constructs and assess DNA loading ability, polydispersity, and both chemical and colloidal stability. Counterintuitively, we demonstrate that polymer hydrolysis from nanomaterial surfaces can occur depending on polymer properties and attachment chemistries, and describe mitigation strategies against construct degradation. Given the growing interest in delivery applications in plant systems, we also assess the toxicity of polymer-based nanomaterials in plants and provide recommendations for future design of nanomaterial-based polynucleotide delivery strategies.

Poly(N-vinylcaprolactam) and Salicylic Acid Polymeric Prodrug Grafted onto Medical Silicone to Obtain a Novel Thermo- and pH-Responsive Drug Delivery System for Potential Medical Devices

New medical devices with anti-inflammatory properties are critical to prevent inflammatory processes and infections in medical/surgical procedures. In this work, we present a novel functionalization of silicone for medical use with a polymeric prodrug and a thermosensitive polymer, by graft polymerization (gamma rays), for the localized release of salicylic acid, an analgesic, and anti-inflammatory drug. Silicone rubber (SR) films were functionalized in two stages using graft polymerization from ionizing radiation (60Co). The first stage was grafting poly(N-vinylcaprolactam) (PNVCL), a thermo-sensitive polymer, onto SR to obtain SR-g-PNVCL. In the second stage, poly(2-methacryloyloxy-benzoic acid) (P2MBA), a polymeric prodrug, was grafted to obtain (SR-g-PNVCL)-g-P2MBA. The degree of functionalization depended on the concentrations of monomers and the irradiation dose. The films were characterized by attenuated total reflectance Fourier-transform infrared spectroscopy (ATR-FTIR), scanning electron microscopy/energy-dispersive X-ray spectrometry (SEM–EDX), thermogravimetric analysis (TGA), and contact angle. An upper critical solution temperature (UCST) of the films was demonstrated by the swelling degree as a temperature function. (SR-g-PNVCL)-g-P2MBA films demonstrated hydrolysis-mediated drug release from the polymeric prodrug, pH, and temperature sensitivity. GC–MS confirmed the presence of the drug (salicylic acid), after polymer hydrolysis. The concentration of the drug in the release media was quantified by HPLC. Cytocompatibility and thermo-/pH sensitivity of functionalized medical silicone were demonstrated in cancer and non-cancer cells.

PEG-Coated Large Mesoporous Silicas as Smart Platform for Protein Delivery and Their Use in a Collagen-Based Formulation for 3D Printing

Silica-based mesoporous systems have gained great interest in drug delivery applications due to their excellent biocompatibility and high loading capability. However, these materials face challenges in terms of pore-size limitations since they are characterized by nanopores ranging between 6–8 nm and thus unsuitable to host large molecular weight molecules such as proteins, enzymes and growth factors (GFs). In this work, for an application in the field of bone regeneration, large-pore mesoporous silicas (LPMSs) were developed to vehicle large biomolecules and release them under a pH stimulus. Considering bone remodeling, the proposed pH-triggered mechanism aims to mimic the release of GFs encased in the bone matrix due to bone resorption by osteoclasts (OCs) and the associated pH drop. To this aim, LPMSs were prepared by using 1,3,5-trimethyl benzene (TMB) as a swelling agent and the synthesis solution was hydrothermally treated and the influence of different process temperatures and durations on the resulting mesostructure was investigated. The synthesized particles exhibited a cage-like mesoporous structure with accessible pores of diameter up to 23 nm. LPMSs produced at 140 °C for 24 h showed the best compromise in terms of specific surface area, pores size and shape and hence, were selected for further experiments. Horseradish peroxidase (HRP) was used as model protein to evaluate the ability of the LPMSs to adsorb and release large biomolecules. After HRP-loading, LPMSs were coated with a pH-responsive polymer, poly(ethylene glycol) (PEG), allowing the release of the incorporated biomolecules in response to a pH decrease, in an attempt to mimic GFs release in bone under the acidic pH generated by the resorption activity of OCs. The reported results proved that PEG-coated carriers released HRP more quickly in an acidic environment, due to the protonation of PEG at low pH that catalyzes polymer hydrolysis reaction. Our findings indicate that LPMSs could be used as carriers to deliver large biomolecules and prove the effectiveness of PEG as pH-responsive coating. Finally, as proof of concept, a collagen-based suspension was obtained by incorporating PEG-coated LPMS carriers into a type I collagen matrix with the aim of designing a hybrid formulation for 3D-printing of bone scaffolds.

Effect of P depletion on the functional pools of diatom carbohydrates, and their utilization by bacterial communities

Phosphorus (P) limitation of phytoplankton growth is known to affect the accumulation and release of carbohydrates (CHO) by micro-algae. However, relatively little is known about the fate of algal exudates, notably their bacterial degradation. The CHO chemical characterization is also not exhaustive, especially in ‘functional’ pools relevant for phytoplankton physiology (particulate reserve [R] or structural [S] CHO) and for bacterial degradation (dissolved mono- [MDCHO] and polysaccharides [P-DCHO]). In this study, we investigated how P depletion and repletion affect the CHO composition in diatom Thalassiosira weissflogii cultures, and the shortterm response of free and diatom-attached bacteria in terms of abundance and potential βglucosidase activity (βGlc). The bacterial inoculum was composed of the bacterial consortiums of diatom precultures and a natural bacterial community from the Bay of Brest. P depletion favored CHO accumulation in diatom cells, mainly as R i.e. soluble CHO accumulated in cytoplasm, but also as S, polysaccharides linked to the cell wall. The R:S ratio was high in the present diatom cultures. The high M-DCHO observed in P-deplete cultures (twice that of P-replete cultures) when P-DCHO remained quite similar is explained both by active polysaccharide hydrolysis (very high potential βGlc of attached bacteria) and reduced uptake of M-DCHO by Pdepleted bacteria. P depletion of heterotrophic bacteria favors labile CHO accumulation, which may affect particle potential aggregation. However, the remarkably constant M-DCHO concentration over time for both conditions suggests tight coupling between phytoplankton accumulation, release, polymer hydrolysis and monomer uptake by bacteria.

Microbial Organic Matter Degradation Potential in Baltic Sea Sediments Is Influenced by Depositional Conditions andIn SituGeochemistry

ABSTRACTGlobally, marine sediments are a vast repository of organic matter, which is degraded through various microbial pathways, including polymer hydrolysis and monomer fermentation. The sources, abundances, and quality (i.e., labile or recalcitrant) of the organic matter and the composition of the microbial assemblages vary between sediments. Here, we examine new and previously published sediment metagenomes from the Baltic Sea and the nearby Kattegat region to determine connections between geochemistry and the community potential to degrade organic carbon. Diverse organic matter hydrolysis encoding genes were present in sediments between 0.25 and 67 meters below seafloor and were in higher relative abundances in those sediments that contained more organic matter. New analysis of previously published metatranscriptomes demonstrated that many of these genes were transcribed in two organic-rich Holocene sediments. Some of the variation in deduced pathways in the metagenomes correlated with carbon content and depositional conditions. Fermentation-related genes were found in all samples and encoded multiple fermentation pathways. Notably, genes involved in alcohol metabolism were amongst the most abundant of these genes, indicating that this is an important but underappreciated aspect of sediment carbon cycling. This study is a step towards a more complete understanding of microbial food webs and the impacts of depositional facies on present sedimentary microbial communities.IMPORTANCESediments sequester organic matter over geologic time scales and impact global climate regulation. Microbial communities in marine sediments drive organic matter degradation, but the factors controlling their assemblages and activities, which in turn impact their role in organic matter degradation, are not well understood. Hence, determining the role of microbial communities in carbon cycling in various sediment types is necessary for predicting future sediment carbon cycling. We examined microbial communities in Baltic Sea sediments, which were deposited across various climatic and geographical regimes to determine the relationship between microbial potential for breakdown of organic matter and abiotic factors, including geochemistry and sediment lithology. The findings from this study will contribute to our understanding of carbon cycling in the deep biosphere and how microbial communities live in deeply buried environments.

Morphological, chemical and structural characterization of silica-containing polyvinylpyrrolidone electrospun nanofibers prepared by sol-gel technique

Purpose: The aim of this study was to produce poly(vinylpyrrolidone) (PVP) containingsilica nanofibers using electrospinning method from 10% PVP/EtOH solutions with differentmass concentration 0 and 30% of tetraethoxysilane. Sol-gel technique was used to obtainnanofiber membranes with high amount of inorganic phase. In the case when metal alkoxide,such as tetraethyl orthosilicate (TEOS) is mixed with an organic polymer, hydrolysis andcondensation reaction of TEOS occur in-situ with polymer matrix, which allows to fabricateorganic-inorganic hybrid structures with uniform dispersion.Design/methodology/approach: The examination of the morphology of the obtainedPVP/silicon dioxide nanofibers using scanning electron microscope (SEM) has been made.The chemical structure of produced nanostructures was investigated by Fourier - TransformInfrared spectroscopy (FTIR) and Energy Dispersive Spectrometry (EDX) to analyze theregular dispersion by examining types of bonds occurring between polymer matrix and SiO2phase.Findings: Results obtained in this paper shows that the mass concentration of thereinforcing phase in form of TEOS have an influence on the average diameter of nanofibersand with the increase of tetraethyl orthosilicate in solution nanofibers diameters decrease.Moreover, structural examination shows uniform dispersion of the reinforcing phase in hybridmaterials.Research limitations/implications: Uniform dispersion of the reinforcing phase insilica-containing PVP nanofibers gives the opportunity to make nanowires in calcinationprocess from such obtained fibrous mats and use in novel electrical devices.Originality/value: This paper describes an easy and more effective way of makingpolymer nanofibers with the content of silicon dioxide with the perspective way of makingsilica nanowires in the future from obtained hybrid nanofibers, so that this method canreplace commonly used nanowires growth processes.

Test and Analysis of Heat-Resistant Polymer Solution’s Hydrolysis

This paper research the hydrolysis law of BH heat-resistant polymer in distilled water, oil field clear water and oil field waste water, and inspect its long-term thermal stability in the waste water. The results showed that there is few difference about hydrolysis degree between the ZIIordinary polymer and BH heat-resistant polymer in distilled water. BH heat-resistant polymer will hydrolyze faster in the waste water than in the clear water. The hydrolysis degree of different concentrations of BH of polymer solution under the same temperature increases with the increase of aging time, the higher the polymer concentration, the higher the viscosity of the solution, the smaller the hydrolysis degree. BH heat-resistant polymer hydrolysis under high temperature will increase, caused the increase of hydrolysis degree from 95°C to 120°C. AMPS group of BH heat-resistant polymer will not hydrolyze under 95°C.