Stable Suspension Research Articles

Generation of stable suspension producer cell lines for serum-free lentivirus production.

The production of lentiviral vectors (LVs) pseudotyped with the vesicular stomatitis virus envelope glycoprotein (VSV-G) is limited by the associated cytotoxicity of the envelope and by the production methods used, such as transient transfection of adherent cell lines. In this study, we established stable suspension producer cell lines for scalable and serum-free LV production derived from two stable, inducible packaging cell lines, named GPRG and GPRTG. The established polyclonal producer cell lines produce self-inactivating (SIN) LVs carrying a WAS-T2A-GFP construct at an average infectious titer of up to4.64×107TU mL-1in a semi-perfusion process in a shake flask and can be generated in less than two months. The derived monoclonal cell lines are functionally stable in continuous culture and produce an average infectious titer of up to 9.38×107TU mL-1in a semi-perfusion shake flask process. The producer clones are able to maintain a productivity of>1×107TUmL-1day-1for up to 29 consecutive days in a non-optimized 5L stirred-tank bioreactor perfusion process, representing a major milestone in the field of LV manufacturing. As the producer cell lines are based on an inducible Tet-off expression system, the established process allows LV production in the absence of inducers such as antibiotics. The purified LVs efficiently transduce human CD34+ cells, reducing the LV quantities required for gene and cell therapy applications.

Synthesis, Characterization and Thermal Studies of Composite Nanofluids and their Comparison with Hybrid Nanofluids

Ternary nanofluids can either be an admixture of three distinct nanoparticles or the dispersion of a ternary nanocomposite in a base fluid. This work focuses on the synthesis, morphological characterization, stability analysis, estimation and optimization of thermophysical parameters of ternary nanofluids consisting of multiwalled carbon nanotubes, graphene oxide and silver (CNT-GO-Ag). Two cases are considered and compared viz. (i) hybrid nanofluids (HNF) prepared from monofluids and (ii) composite nanofluids (CNF) prepared by the dispersion of ternary nanocomposites. The CNF was found to have an enhanced thermal conductivity ratio (knf/kb) of 40% as compared to 30% for HNF at 30 ºC. This enhancement for the CNF and HNF were found to be 45% and 32%, respectively at the electronic cooling exposure temperature of ~40 to 50 ºC. The zeta potential analysis also proved that CNF had superior suspension stability than HNF. The viscosity of CNF was found to be 8% (at 20 ºC) to 20% (at 80 ºC) lower than HNF, much desired for fluid flow characteristics. Overall, the results show that CNF as compared to HNF possesses superior thermophysical properties with good potential for application in electronic cooling studies.

The suspension stability of nanoplastics in aquatic environments revealed using meta-analysis and machine learning

Nanoplastics (NPs) aggregation determines their bioavailability and risks in natural aquatic environments, which is driven by multiple environmental and polymer factors. The back propagation artificial neural network (BP-ANN) model in machine learning (R2 = 0.814) can fit the complex NPs aggregation, and the feature importance was in the order of surface charge of NPs > dissolved organic matter (DOM) > functional group of NPs > ionic strength and pH > concentration of NPs. Meta-analysis results specified low surface charge (0 ≤ |ζ| < 10 mV) of NPs, low concentration (< 1 mg/L) and low molecular weight (< 10 kg/mol) of DOM, NPs with amino groups, high ionic strength (IS > 700 mM) and acidic solution, and high concentration (≥ 20 mg/L) of NPs with smaller size (< 100 nm) contribute to NPs aggregation, which is consistent with the prediction in machine learning. Feature interaction synergistically (e.g., DOM and pH) or antagonistically (e.g., DOM and cation potential) changed NPs aggregation. Therefore, NPs were predicted to aggregate in the dry period and estuary of Poyang Lake. Research on aggregation of NPs with different particle size,shapes, and functional groups, heteroaggregation of NPs with coexisting particles and aging effects should be strengthened in the future. This study supports better assessments of the NPs fate and risks in environments.

Cyrene- and water-based exfoliation of black phosphorus for potential nanolayer-mediated disaggregation of insulin fibrils

Liquid suspensions of phosphorene nanolayers (2D-bP) obtained through liquid phase exfoliation (LPE) of elemental black phosphorus (bP) have been prepared and extensively characterized. The exfoliating ability of deionized water (DI water), dihydrolevoglucosenone, (Cyrene), and N-methyl-2-pyrrolidone (NMP) has been investigated and compared along with the differences in the structure, concentration, and stability of the collected nanoflakes. Water was chosen as an exfoliating medium due to its harmlessness and cost-effectiveness and because it is the safest solvent for further potential biomedical applications. Cyrene is a new bio-based solvent still under study. NMP, which is among the most widely used solvents for the exfoliation of 2D systems including bP, has been employed for comparison. The obtained suspensions have been characterized by Dynamic Light Scattering (DLS), Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES), Phosphorus 31 Nuclear Magnetic Resonance (31P NMR), Transmission Electron Microscopy (TEM), Ultraviolet -Visible (UV–Vis), and Raman spectroscopies. The stability of 2D-bP suspensions over time and their photoactivity, i.e., their ability to generate singlet oxygen species as a photosensitizer, have been investigated. The collected results evidenced that the exfoliation of bP in different solvents, including DI water, resulted in satisfactory and comparable nanoflake structures and features. The singlet oxygen generation through irradiation of 2D-bP in DI water suspensions, advantageously obtained directly from LPE, showed promising potential for use in photodynamic therapy (PDT). Preliminary data on the potential biomedical application of 2D-bP to inhibit the insulin self-assembly into amyloid aggregates as well as to cause fibrils disassembling through simple incubation or photoactivity, are also discussed.

Mucoadhesion, Rheology, Swelling Behavior, and Immunomodulatory Properties of Polysaccharides of Gum Exudates Obtained from Astracantha echidnaeformis (Sirj.) Podlech as a Formulary Excipient Candidate

AbstractThe physicochemical, rheological, and mucoadhesive characteristics of gum derived from Astracantha echidnaeformis are investigated. It's polysaccharides are isolated using chromatography techniques, and their immunomodulatory characteristics are evaluated by subjecting Jurkat cells to the WST‐1 assay. The composition of these polysaccharides is analyzed using gas chromatography‐mass spectrometry (GC‐MS). The viscosity and shear‐thinning behavior of gum are directly influenced by its concentration and the presence of NaCl, whereas they are inversely affected by temperature. The gum has strong potential as a thickening agent for dispersed systems. The mucoadhesion strength of the gum insoluble fraction is 109 ± 4.58 g cm−2, indicating excellent adhesiveness for application to mucoadhesive formulations. Cells’ proliferation enhancement is found for the isolated manno‐arabinoglucan (MW: ≤1.27 kDa) and galacto‐arabinan (MW: ≥667.8 kDa) at concentrations lower than 400 µ mL−1, but at higher concentrations they inhibited the proliferation. The isolated pectic galacto‐arabinan (MW: 669.58 kDa) exhibited a proliferative effect at 250 µg mL−1, but the isolated manno‐galactoglucan (MW: 80.90 kDa) showed cytotoxicity at higher doses. The isolated proteoglycans has mostly galacto‐arabinan backbones with immunomodulatory properties. The gum can be used as a thickening agent for the physical stabilization of suspensions and gels, specifically those needing to be stored at cold temperatures.

Effects of Ultrasonic Treatment on Physical Stability of Lily Juice: Rheological Behavior, Particle Size, and Microstructure.

The aim of this study was to investigate the rheological properties, particle size distribution, color change, and stability of lily juice under different ultrasonic treatment conditions (152 W, 304 W, 456 W, 608 W, and 760 W). The results showed that the lily juice exhibited non-Newtonian shear thinning behavior, and the viscosity decreased with the increase in ultrasonic power. Under ultrasonic treatment conditions, there was no significant change in the pH value and zeta potential value of the samples. The content of cloudy value and total soluble solids (TSS) increased gradually. However, both the sedimentation components and centrifugal sedimentation rate showed a downward trend and an asymptotic behavior. In addition, high-power ultrasound changed the color index (L* value decreased, a* value increased), tissue structure, and particle distribution of the sample, and small particles increased significantly. To sum up, ultrasonic treatment has great potential in improving the physical properties and suspension stability of lily juice.

Aggregation-Induced Emission of Naphthalene Diimides: Effect of Chain Length on Liquid and Solid-Phase Emissive Properties.

The aggregation-induced emission (AIE) properties of a systematic series of naphthalene diimides (NDIs) varying the chain length at the imide positions have been studied. A solvophobic collapse of NDI units through the flash injection of THF NDI solutions in sonicating water triggers the formation of stable suspensions with enhanced fluorescence emissions. Shorter chains favor the π-π stacking of NDI units through H-aggregation producing a strong AIE effect showing remarkably high quantum yields that have not been observed for non core-substitued NDIs previously. On the other hand, NDIs functionalized with longer chains lead to more disordered domains where π-π stacking between NDI units is mainly given by J-aggregation unfavoring the AIE effect.

Novel surface modification strategies for enhanced CeO2 nanoparticle dispersion and suspension stability

This work aims to modify the surface characteristics of cerium oxide (ceria, CeO2) nanoparticles using different surface modification strategies for improved CeO2 nanoparticle dispersion and suspension stability. Analysis and discussion were conducted on the two surface modification processes used by a cationic surfactant like hexadecyl cetyltrimethylammonium bromide (CTAB) and a silane agent like tetraethyl orthosilicate (TEOS). Untreated CeO2 was used as reference material. The dispersion effect of surface-modified CeO2 nanoparticles at different pHs was determined by zeta potential measurements. Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), Particle size analysis (PSA), Thermogravimetric analysis (TGA), Scanning electron microscope (SEM), Brunauer–Emmett–Teller analysis (BET), and X-ray diffraction (XRD) were used to confirm the efficacy of the surface modification of CeO2 nanoparticles. First, the results obtained in this experimental work demonstrate that both advanced modifications greatly enhance the dispersion and suspension stability of surface-modified CeO2 nanoparticles in comparison with untreated CeO2 nanoparticles. Second, it is also shown that the surface-modified CeO2 nanoparticles obtained through a silanization surface process with TEOS silane agent had a better dispersion effect and dispersion stability than the surface-modified CeO2 nanoparticles obtained by surface modification with CTAB cationic surfactant. These results can help better understand how advanced surface modifications can assist the application of well-dispersed CeO2 nanoparticles in technological applications.

Secondary Atomization and Micro-Explosion Effect Induced by Surfactant and Nanoparticles on Enhancing the Combustion Performance of Al/JP-10/OA Nanofluid Fuel.

Aluminum/tetrahydrodicyclopentadiene/oleic acid (Al/JP-10/OA) nanofluid fuel is considered a potential fuel for aircraft powered by aviation turbine engines. However, an optimized formula for an Al/JP-10/OA system inducing a secondary atomization and micro-explosion effect and improving the burning performance needs to be developed. With this aim, in this work, the combustion characteristics of pure JP-10, JP-10/OA, JP-10/Al, and Al/JP-10/OA were experimentally tested, and a comparative analysis was conducted. Specifically, the influence of the surfactant and nanoparticle concentrations on the combustion characteristics of Al/JP-10/OA nanofluid fuel, including the flame structure, the flame temperature, the burning rate, the secondary atomization and micro-explosion effect, etc., were evaluated in detail. The results demonstrate that the addition of OA surfactant and Al nanoparticles had a significant effect on the burning rate of fuel droplets. The OA had an inhibition effect, while the Al nanoparticles had a promotion effect. As both OA and Al nanoparticles were added to the JP-10, the synergetic effect had to be considered. At the optimum ratio of OA to Al for the best suspension stability, there is a critical Al concentration of 1.0 wt.% from promotion to inhibition with increases in the Al concentration. The addition of OA and Al nanoparticles induced the secondary atomization and micro-explosion, resulting in an unsteady combustion and chaotic flame structure. The transient flame temperature of hundreds of Kelvins increased, the high-temperature flame zone widened, and thus, the energy release was elevated. Therefore, the combustion performance and energy release of Al/JP-10/OA nanofluid fuel can be improved through the secondary atomization and micro-explosion effect induced by the surfactant and nanoparticles.

Toward Modeling the Structure of Electrolytes at Charged Mineral Interfaces Using Classical Density Functional Theory.

The organization of water molecules and ions between charged mineral surfaces determines the stability of colloidal suspensions and the strength of phase-separated particulate gels. In this article, we assemble a density functional that measures the free energy due to the interaction of water molecules and ions in electric double layers. The model accounts for the finite size of the particles using fundamental measure theory, hydrogen-bonding between water molecules using Wertheim's statistical association theory, long-range dispersion interactions using Barker and Henderson's high-temperature expansion, electrostatic correlations using a functionalized mean-spherical approximation, and Coulomb forces through the Poisson equation. These contributions are shown to produce highly correlated structures, aptly rendering the layering of counterions and co-ions at highly charged surfaces and permitting the solvation of ions and surfaces to be measured by a combination of short-range associations and long-ranged attractions. The model is tested in a planar geometry near soft, charged surfaces to reproduce the structure of water near graphene and mica. For mica surfaces, explicitly representing the density of the outer oxygen layer of the exposed silica tetrahedra allows water molecules to hydrogen-bond to the solid. When electrostatic interactions are included, water molecules assume a hybrid character, being accounted for implicitly in the dielectric constant but explicitly otherwise. The disjoining pressure between approaching like-charged surfaces is calculated, demonstrating the model's ability to probe pressure oscillations that arise during the expulsion of ions and water layers from the interfacial gap and predict strong interattractive stresses that form at narrow interfacial spacing when the surface charge is overscreened. This interattractive stress arises not due to in-plane correlations under strong electrostatic coupling but due to the out-of-plane structuring of associating ions and water molecules.

On the Feasibility of Rugose Lipid Microparticles in Pressurized Metered Dose Inhalers with Established and New Propellants.

Pressurized metered dose inhalers (pMDIs) require optimized formulations to provide stable, consistent lung delivery. This study investigates the feasibility of novel rugose lipid particles (RLPs) as potential drug carriers in pMDI formulations. The physical stability of RLPs was assessed in three different propellants: the established HFA-134a and HFA-227ea and the new low global-warming-potential (GWP) propellant HFO-1234ze. A feedstock containing DSPC and calcium chloride was prepared without pore forming agent to spray dry two RLP batches at inlet temperatures of 55 °C (RLP55) and 75 °C (RLP75). RLPs performance in pMDI formulations was compared to two reference samples that exhibit significantly different performance when suspended in propellants: well-established engineered porous particles and particles containing 80% trehalose and 20% leucine (80T20L). An accelerated stability study at 40°C and relative humidity of 7% ± 5% was conducted over 3months. At different time points, a shadowgraphic imaging technique was used to evaluate the colloidal stability of particles in pMDIs. Field emission electron microscopy with energy dispersive X-ray spectroscopy was used to evaluate the morphology and elemental composition of particles extracted from the pMDIs. After 2weeks, all 80T20L formulations rapidly aggregated upon agitation and exhibited significantly inferior colloidal stability compared to the other samples. In comparison, both the RLP55 and RLP75 formulations, regardless of the propellant used, retained their rugose structure and demonstrated excellent suspension stability comparable with the engineered porous particles. The studied RLPs demonstrate great potential for use in pMDI formulations with HFA propellants and the next-generation low-GWP propellant HFO-1234ze.

Synthesis of Silver‐Doped Titanium Dioxide Nanoparticles by Sol‐Gel and Coprecipitation Techniques: Evaluation of Antimicrobial Activity and Cytotoxic Effects

AbstractTiO2 nanoparticles are effective alternative to the antibiotics. The quick recombination of the photogenerated charges and the inefficient exploitation of visible light remain the major problems limiting their large‐scale applications. Modifying the TiO2 with Silver that acting as an electron trap, plays an important role in reducing the recombination of TiO2 charges and shift its photo‐response to the visible light region. The present work aims to synthesize AgTiO2 nanoparticles using sol‐gel and coprecipitation methods and evaluating the antimicrobial behavior of them. Also, to find the optimal conditions based on the anatase phase of TiO2 due to its higher antimicrobial activity than the rutile form. Among Ag‐TiO2 nanoparticles obtained, the one prepared by sol‐gel method at 450 °C and PH=8–8.5 exhibits the best antimicrobial property. AgTiO2 nanoparticles have been characterized by means X‐ray Diffraction (XRD), Fourier transform infrared spectroscopy (FTIR),scanning electron microscope (SEM), ζ‐potential, dynamic light scattering (DLS) that showing promising results. Zeta potential values −103 mV has been reported that is considered as a stable colloidal suspension system that prevents nanoparticles aggregation. Antimicrobial behavior of them were evaluated using Diffusion (Agar disk‐diffusion), Dilution (MIC) and Bacterial colony counting methods and diameter of the inhibitory zone 15 mm and minimum inhibitory concentration 5 mg/ml was observed.Colony count results indicated that AgTiO2 able to kill bacteria at the lowest concentration of 5 mg/ml. Outcomes of MTT assay (measure cell cytoxicity) suggesting the absence of toxicity in living Hfff cells (as a normal human fibroblast) while surviving L929 cells (as a cancer cell line originated from mouse fibroblast cells). After 24 and 48 h incubation from 100 % to 77.3 % and 57.2 % was reduced respectively. This indicates that Ag/TiO2 nanoparticles act as a anticancer drug and have inherent selective toxicity nature towards cancer cells while posing no effect to normal cells. AgTiO2 nanoparticles are synthesized using sol‐gel and coprecipitation methods. The sample prepared by the sol‐gel method at a temperature of 450 °C and pH=8.5, which corresponds to the anatase phase of TiO2 synthesis, shows the best antimicrobial properties and acts as an anticancer drug with inherent selective toxicity nature towards cancer cells while posing no effect on normal cells.

Characteristics of Dialdehyde Cellulose Nanofibrils Derived from Cotton Linter Fibers and Wood Fibers.

Two types of cellulose nanofibrils (CNFs) were isolated from cotton linter fibers and hardwood fibers through mechanical fibrillation methods. The dialdehyde cellulose nanofibrils (DACNFs) were prepared through the periodate oxidation method, and their morphological and structural properties were investigated. The characteristics of the DACNFs during the concentration process were also explored. The AFM analysis results showed that the mean diameters of wood fiber-based CNFs and cotton fiber-based CNFs were about 52.03 nm and 69.51 nm, respectively. However, the periodate oxidation treatment process obviously reduced the nanofibril size and destroyed the crystalline region of the nanofibrils. Due to the high crystallinity of cotton fibers, the cotton fiber-based DACNFs exhibited a lower aldehyde content and suspension stability compared to the wood fiber-based DACNFs. For the concentration process of the DACNF suspension, the bound water content of the concentrated cotton fiber-based DACNFs was lowered to 0.41 g/g, which indicated that the cotton fiber-based DACNFs could have good redispersibility. Both the wood fiber-based and cotton fiber-based DACNF films showed relatively good transmittance and mechanical strength. In addition, to the cotton fiber-based DACNF films had a very low swelling ratio, and the barrier water vapor and oxygen properties of the redispersed cotton fiber-based DACNF films decreased by very little. In sum, this study has demonstrated that cotton fibers could serve as an effective alternative to wood fibers for preparing CNFs, and that cotton fiber-based DACNFs have huge application prospects in the field of packaging film materials due to their stable properties during the concentration process.

Synthesis and characterization of cellulose nanofibers from waste paper and their utilization in wood adhesion

AbstractNanocellulose extraction from lignocellulosic materials is a highly chemical and energy‐intensive process as it requires the removal of lignin and hemicellulose. Writing paper is one of the processed materials that could be used as a raw material for the extraction of nanocellulose. In this work, cellulose nanofibers (CNFs) were synthesized from paper waste using TEMPO‐oxidation followed by high‐shear microfluidization. Scanning electron microscopy and atomic force microscopy confirmed the diameter of fibers in the nano‐range and a consistent zeta potential confirmed the stability of CNF suspension in water over a long time frame. Characterization of the CNFs using Fourier transform infrared spectroscopy indicated the presence of a carbonyl group due to the oxidation process. Thermogravimetric analysis and x‐ray diffraction revealed lower thermal stability and reduction in the crystallinity index of CNFs, as compared to pulp fibers. The obtained CNFs were used successfully as the sole binding agent in the preparation of fiberboards and also utilized as a reinforcing agent for polyvinyl acetate (PVAc) adhesive in the preparation of laminated veneer lumber (LVLs). The addition of CNFs in PVAc improved the glue shear strength indicating superior bonding characteristics and also increased the water resistance of the LVLs.Highlights This work focused on cellulose nanofibers (CNFs) extraction from waste paper Obtained CNFs form stable water suspension and have a diameter of less than 15 nm Thermal stability and crystallinity index reduced after conversion to nanofibers CNFs form a complex network and act as a sole binder to make fiberboards CNFs were utilized as a reinforcing agent for PVAc in preparation of LVLs

Evaluation of the Effect of Polyethylenimine on Boron Adsorption by Soil Minerals.

The removal of hazardous ions from water is crucial for safeguarding both the environment and human health. Soil minerals, integral components of soil, play a vital role as adsorbents for various contaminants, including heavy metal ions, organic dyes, and detergents. This study investigates the interaction between boron ions and soil minerals (gibbsite, kaolinite, and montmorillonite) in the presence of polyethylenimine (PEI). The minerals underwent characterization based on specific surface area, particle size distribution, zeta potential, and the presence of functional groups. The influence of PEI addition on the stability of the soil mineral suspension was evaluated by turbidimetry. Mineral-boron and mineral-boron-PEI interactions were explored under varying conditions, including pH, initial boron concentration, and mineral quantity, with all adsorption experiments conducted over 24 hours. Using the Langmuir isotherm, the maximum adsorption capacity of the studied minerals was determined for boron both without and in the presence of PEI. For gibbsite, kaolinite and montmorillonite, it was 30.63, 24.55 and 26.62 mg g-1, respectively, while in the presence of PEI, it increased to 33.11, 26.61 and 45.47 mg g-1, respectively. The addition of PEI enhanced boron adsorption from aqueous solutions, increasing the removal efficiency from 65 % to about 80 %.

Mesoporous Nitrogen-Doped Holey Reduced Graphene Oxide: Preparation, Purification, and Application for Metal-Free Electrochemical Sensing of Dopamine.

Holey graphenic nanomaterials with porosity within the basal plane attract significant interest. It is observed that the perforation of graphene can enhance the specific surface area of the nanosheet, ensuring effective wetting and penetration of electrolytes to the electrode surface, facilitating rapid charge transfer, and boosting the electrocatalytic efficacy of the transducers. This study reports the first example of nitrogen-doped holey reduced graphene oxide with a mesoporous morphology of the graphene basal plane (N-MHG). It is shown that N-MHG can be synthesized through a one-step hydrothermal treatment of GO using NH3 and H2O2. A straightforward procedure for the purification of N-MHG has also been developed. AFM, TEM, and Raman analyses have revealed that N-MHG possesses a highly mesoporous network structure with a pore size ranging from 10 to 50 nm. X-ray photoelectron spectroscopy data have indicated a partial reduction of the graphene oxide sheets during the etching process but also show a 3-5 times higher content of C═O and O-C═O fragments compared to rGO. This could account for the remarkable stability of the N-MHG aqueous suspension. An electrochemical sensor for dopamine analysis is assembled on a glassy carbon electrode with N-MHG/Nafion membrane and characterized by cyclic voltammetry and electrochemical impedance spectroscopy.

Effects of dynamic high pressure microfluidization on the physical and chemical properties of carrot (Daucus carota L.)

Effects of dynamic high-pressure micro-fluidization (DHPM) on the physical and chemical properties of carrot juice was investigated in the present study. Carotene content, turbidity, centrifugal sedimentation rate, soluble solids content, color, and particle size and distribution of the samples homogenized with different pressures were evaluated. When compared with the control sample, carotene content, turbidity, suspension stability, centrifugal sedimentation rate, color, and particle size and distribution of the carrot juice showed a significant difference at different pressures. The result indicated that DHPM could improve the physical and chemical properties of carrot juice, such as increased carotene content, stability and affecting color positively resulting in a desirable high-quality juice for the consumer. Bangladesh J. Bot. 53(1): 123-129, 2024 (March)

Electrophoretic deposition of tea tree oil containing chitosan/gelatin/whitlockite composite coatings for biofilm protection and bone tissue regeneration

This work presents a design of experiment (DoE) approach to optimize the electrophoretic deposition (EPD) parameters for chitosan (CS), gelatin (Gel), and whitlockite (WH) composite coatings on titanium substrate. The suspension for EPD was prepared by dissolving CS and Gel in acetic acid and WH nanoparticles (NPs) were dispersed in ethanol. Afterward, both (CS, Gel solution, and WH suspension) were mixed and the suspension stability was evaluated using zeta potential. Deposition parameters like voltage, concentration of WH, and time were optimized using Taguchi L16 orthogonal array with four control factors. The statistical data obtained confirmed that a higher time with average voltage and WH concentration is ideal to achieve deposits with maximum yield and minimum signal-to-noise ratio. Tea tree oil (TTO) in different concentrations was added to these optimized conditions. Different physiochemical characterization like x-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), in-vitro degradation, surface adhesion, and wettability tests were done to evaluate the coating stability, adhesion, surface and chemical properties. The obtained data confirmed that coatings were mechanically strong, chemically stable, and possessed good adhesion strength to the substrate. To further confirm the bone tissue regeneration potential of the coatings, in-vitro bioactivity, cell viability, and cell proliferation tests were done. The obtained data confirmed that CS/Gel/WH composite is highly bioactive and promotes osseointegration. TTO at lower concentrations facilitates cell proliferation but it is toxic at higher concentrations. TTO interacted with the coating matrix via non-covalent interactions that resulted in its slow and sustained release over 28 days. TTO showed antibacterial effect when tested with E. coli bacteria. Hence, in this work, experimental, statistical, physiochemical, and biological analyses are discussed in detail based on the current knowledge of WH coatings and the effect of TTO on cytocompatibility as well as biofilm prevention.

Modification mechanism of calcium lignosulfonate on cementing cement

During the construction of coalbed methane extraction wells, cementing cement sheath is crucial for the stability and sealing of surface wells. One effective method to enhance these properties is the addition of lignosulfonate. However, the mechanism of the effect of calcium lignosulfonate on the whole process of cement hydration is still unclear. In this paper, the water distribution and variation characteristics of calcium lignosulfonate modified cement paste were revealed by low-field nuclear magnetic resonance technology, and the hydration ion experiment of modified cement was carried out to obtain the variation characteristics of hydration ions of modified cementing cement. Finally, the formation mechanism of hydration products was clarified by analyzing the phase change of modified cement stone. The results indicate that the cement paste’s hydration process can be divided into four stages: dissolution, crystallization, acceleration, and decline. During the dissolution stage, calcium lignosulfonate’s air entraining effect maintains the cement paste in a stable suspension state. In the crystallization stage, calcium lignosulfonate’s electro-repulsion delays the formation of hydration products and the hydration process. During the acceleration stage, the addition of calcium lignosulfonate reduces bound water formation in the cement slurry’s flocculation structure, and the released filled water participates more in the hydration reaction, reducing the total relaxation signal’s increasing trend. In the decline stage, the cement paste has solidified, and the system’s water is primarily in the porous medium. The research results have practical guiding significance for the addition of calcium lignosulfonate in cementing operations.

Sodium dodecyl sulphate-treated nanohydroxyapatite as an efficient shale stabilizer for water-based drilling fluids

Drilling water-sensitive shale formations often leads to wellbore instability, resulting in drilling problems because of the clay's high-water affinity. To solve this problem, different nanoparticles (NPs), such as nanosilica, have been used to formulate water-based muds with potassium chloride (KCl-WBM). Nevertheless, the unmatched pore size of shale pores when using nanosilica fails to completely prevent shale swelling and dispersion. This study discusses the effects of KCl-WBM with sodium dodecyl sulphate-treated nanohydroxyapatite (nHAp/SDS) on shale swelling inhibition through various laboratory techniques. These techniques encompass the linear swell meter (LSM), the dynamic linear swell meter (DLSM), hot-rolling dispersion, suspension stability, and pore structure characterization of shale. The rheological and filtration characteristics of nHAp/SDS and compatibility tests were also studied, and the results were compared with those of nanosilica and KCl-WBM. At all concentrations, the performance of the nHAp/SDS test fluids surpassed that of nanosilica. When compared with KCl-WBM system at 10 cP and 25 °C, the nHAp/SDS and nanosilica concentrations increased the plastic viscosity by 20–90 % and 10–70 %, respectively. The inhibitory effect of nHAp/SDS surpasses that of conventional KCl-WBM and inorganic nanosilica. By adding 2.0 wt% nHAp/SDS to KCl-WBM, the shale swelling decreased from 10.1 to 4.7 % (a 53.4 % reduction). Nanosilica also reduced the swelling to 6.1 % (a 39.6 % reduction) during the LSM test at 25 °C. Under the DLSM test conditions, the shale swelling increased due to the activation of the clay platelet site at an increased temperature of 80 °C. For instance, between 25 and 80 °C, the DLSM test revealed that the shale plug height expanded from 6.1 to 9.8 % for 2.0 wt% nanosilica, 4.7–7.6 % for 2.0 wt% nHAp/SDS, and 10.1–18.8 % for KCl-WBM. Furthermore, the recovery rate of hot-rolled shale plugs with KCl-WBM increased from 89.8 to 96.2 % for nHAp/SDS and 76.6 to 88.8 % for nanosilica from the initial rates of 52.1–63.3 % between 65 and 120 °C. The contact angle results showed that nHAp/SDS is hydrophobic, reducing shale-water attraction. Moreover, the 12 nm nanosilica matches nanopore sizes to partially block shale pores. This research found that nHAp/SDS has the potential to improve wellbore stability.