Stable Suspension Research Articles

Study on synthesis and mechanism of high temperature resistant suspension stabilizer for spacer fluid

With 2-acrylamido-2-methylpropanesulfonic acid (AMPS), YX-1 (a monomer containing an amide group) as the main chain, DX-2 (a monomer containing a hydrophobic group), N-vinylpyrrolidone (NVP) as the side chain, the high temperature resistant suspension stabilizer for spacer was prepared by free radical aqueous solution polymerization and characterized. The structure was characterized by fourier transform infrared (FTIR) spectroscopy and thermogravimetry-differential thermal analysis (TG-DTA), which proved that the synthesized product was the target product. The performance of the copolymer was evaluated. The experimental results showed that it could be used in the spacer fluid at 30 ∼ 210 °C, and its sedimentation performance could also meet the requirements in the spacer fluid system containing saturated brine. In order to explore the mechanism of the polymer, the polymer solution was tested by six-speed rotational viscometer, pyrene fluorescence probe test, environmental scanning electron microscopy (ESEM) test, and the isolation solution containing the copolymer was tested by Zeta potential test and X-ray diffraction (XRD). Based on the above test results, it is shown that the suspension stabilizer synthesized in this paper has the characteristics of thickening, physical plugging, chemical and physical adsorption, which can effectively ensure that the spacer fluid has excellent suspension performance at high temperature.

High-yield preparation of g-C3N4 nanosheet suspension by a two-step mechanochemical technique

Compared with the bulk g-C3N4, g-C3N4 nanosheets have the advantages such as larger specific surface area and more active sites, making them more promising in optoelectronic applications. However, the current methods for preparing g-C3N4 nanosheets have some disadvantages such as low yield, long exfoliation time and high energy consumption. Herein, a two-step mechanochemical method combining wet ball milling with ultrasonic-ball milling has been proposed, with a high yield of up to 31.8% for suspensible g-C3N4 nanosheets. Adding YSZ balls during the ultrasound process can effectively improve the cutting efficiency of the g-C3N4 sheets, thereby increasing the yield of the suspensible nanosheets. The stability of g-C3N4 suspensions were relatively high, and the concentration of the suspensions remained above 87% after standing 24 h. The spectra of the nanosheets obtained through the two-step process had a single emission peak of 435 nm, which was suitable for photoluminescence detection.

A novel low molecular weight thermal response suspension stabilizer for oil well cement in high temperature environment: Synthesis, behavior and mechanism research

To solve solid particle sedimentation of cement slurry under high temperatures, a novel low molecular weight thermal-responsive copolymer was synthesized as a suspension stabilizer by free radical polymerization. The structure and performance of the suspension stabilizer were investigated by in-situ infrared spectroscopy, ultraviolet–visible spectroscopy, etc. The results revealed that the suspension stabilizer has thermal-responsive characteristics and excellent thermal stability. After adding 0.1% suspension stabilizer, the solids suspension stability of cement slurry was improved with a density difference ≤0.02 g cm−3 under 200 °C, and cement slurry exhibited limited viscosity increasing at low and high temperatures.

Functional insights into the interaction of Lactobacillus spp. and potentially protective agents

The research addresses the critical need to explore how potentially protective agents (PPAs) influence the cellular characteristics of probiotic bacteria, with a focus on strain-specific responses. This study aimed to reveal the effect of 48-h exposure of the Lactobacillus spp. strains to selected PPAs on the viability, metabolic activity, stress response, surface properties, and physicochemical stability of bacterial suspensions. Results provide new insights into the potential risks or benefits of using the tested PPAs in probiotic production based on the analyzed strains, offering valuable information on their impacts on bacterial cells. Trehalose (TRE) and vitamin C (VC) notably impact the metabolic activity and surface characteristics of cells, with TRE improving viability and VC changing surface roughness and particle size distribution (PSD), suggesting a delicate balance between stress induction and viability enhancement. Inulin (IN) decreased metabolic changes, pointing the complex interplay between PPAs and bacterial metabolism. Results of zeta potential and PSD measurements revealed that other PPAs can either promote uniformity or induce aggregation of the bacterial suspensions. Findings have shown significant strain-specific effects of PPAs on bacterial viability and functionality, suggesting that their careful selection can improve bacterial health. Future directions include exploring the molecular mechanisms behind PPAs' effects and their practical applicability in real food systems.

Correlation between zeta potential and electron paramagnetic resonance of thulium, europium co-doped yttria based suspensions

The formation of advanced ceramic components with homogeneous microstructure and functional characteristics demands a suitable control of particle dispersion. Thus, the characterization of particle stability as immersed in a liquid medium is important. The present paper reports an approach to evaluate the stability of europium, thulium co-doped yttria (YET) nanoparticles by a correlation between zeta potential and Electron Paramagnetic Resonance (EPR) techniques. Based on results, YET suspensions exhibited high stability apart from pH 10, while their isoelectric point presented a slight variation from pHIEP 8.5 to 9.2 according to thulium content 0 and 2 at.%, respectively. The peak-to-peak amplitude of EPR spectra of the YET suspensions increased as pH shifted toward alkaline condition, following zeta potential curves features. The present achievements are very useful parameters to form stable suspensions based on rare-earth oxides and to advance toward new materials for radiation dosimetry.

Tribological performance of di-n-octyl sebacate synthesized with carboxylated nano-MoS2/sericite as catalyst

PurposeThis study aims to explore the synthesis and tribological performances of di-n-octyl sebacate (DOS) synthesized with spherical nano-MoS2/sericite (SMS) and carboxylated SMS (CSMS) as catalysts.Design/methodology/approachSMS and CSMS were used as esterification catalysts to synthesize DOS from sebacic acid and n-octanol. The two catalysts were in situ dispersed in the synthesized DOS after the reaction to form suspensions. The tribological performances of the two suspensions after 20 days of storage were studied.FindingsCSMS was more stably dispersed in DOS than SMS, and they reduced friction by 55.6% and 22.2% and wear by 51.3% and 56.5%, respectively. Such results were mainly caused by the COOH on CSMS, which was more conducive to improving the dispersion and friction reduction of CSMS than wear resistance. Another possible reason was the difference between the dispersion amounts of CSMS and SMS in DOS. The sericite of SMS was converted into SiO2 to enhance wear resistance, while that of CSMS only partially generated SiO2, and the rest still remained on the surface to reduce friction.Originality/valueThis work provides a more effective SMS catalytical way for DOS synthesis than the traditional inorganic acid catalytical method. SMS does not need to be separated after reaction and can be dispersed directly in DOS as a lubricant additive. Replacing SMS with CSMS can produce a more stable suspension and reduce friction significantly. This work combined the advantages of surface carboxylation modification and in situ catalytic dispersion and provided alternatives for the synthesis of DOS and the dispersion of MoS2-based lubricant additives.

Dyeing of polyacrylonitrile knitted fabric using liposomes

In this study, it was aimed to analyze the effects of liposomes on the dyeing of polyacrylonitrile fabrics. For this purpose, firstly liposome synthesis was carried out, and then liposome production was confirmed by Fourier transform infrared spectroscopy analysis. Additionally, zeta potential measurements were carried out to see whether stable structures were formed. Then, a selected basic dye was encapsulated with a liposome and the possibilities of using these capsules as alternative to retarders in the dyeing of polyacrylonitrile fabrics were examined. According to results obtained, it can be said that the 1% solution of synthesized liposomes creates a more stable suspension with a polydispersity index of 0.472 and the average particle size of 165.2 nm. On the other hand, it has been revealed that if 1% liposome is used in dyeing, a kind of retarder effect can be achieved in the dyeing of polyacrylonitrile fabrics. Moreover, it can be said that the decrease in color efficiency, that is, the loss of yield, caused by the use of liposome at the end of dyeing is lower compared to the retarder. This is also a very important issue, because a good retarder is expected to slow down the dye uptake, but not reduce the dye intake too much at the end of the dyeing. Dyeing levelness (%) was found to be 96.1, 97.4, and 97.1 for dyeings without auxiliary, with 1% cationic retarder and with 1% liposome, respectively. Beyond this, no significant difference was observed in terms of fastness of dyeing.

Tuning the Properties of Xylan/Chitosan-Based Films by Temperature and Citric Acid Crosslinking Agent.

Petroleum-based food packaging causes environmental problems such as waste accumulation and microplastic generation. In this work, biobased films from stable polyelectrolyte complex suspensions (PECs) of xylan and chitosan (70 Xyl/30 Ch wt% mass ratio), at different concentrations of citric acid (CA) (0, 2.5, 5, 7.5 wt%), were prepared and characterized. Films were treated at two temperatures (135 °C, 155 °C) and times (30 min, 60 min) to promote covalent crosslinking. Esterification and amidation reactions were confirmed by Fourier Transform Infrared Spectroscopy and Confocal Raman Microscopy. Water resistance and dry and wet stress-strain results were markedly increased by thermal treatment, mainly at 155 °C. The presence of 5 wt% CA tended to increase dry and wet stress-strain values further, up to 88 MPa-10% (155 °C for 60 min), and 5.6 MPa-40% (155 °C for 30 min), respectively. The UV-blocking performance of the films was improved by all treatments, as was thermal stability (up to Tonset: 230 °C). Contact angle values were between 73 and 84°, indicating partly wettable surfaces. Thus, thermal treatment at low CA concentrations represents a good alternative for improving the performance of Xyl/Ch films.

Synthesis of suspension stabilizers for isolation fluids by response surface methodology and study of their properties

In order to solve the problem of unstable settling of isolation fluid at high temperatures, high-temperature-resistant suspension stabilizers for isolation fluids were prepared. Using the free radical aqueous solution method with 2-acrylamido-2-methylpropanesulfonic acid (AMPS), YX-1 (a monomer containing an amide group) as the main chain of the molecule, and N-Vinylpyrrolidone (NVP) and DX-2 (monomer containing hydrophobic groups) as the side chains of the molecule. We innovate the suspension stabilizer synthesis process, the synthesis conditions of the suspension stabilizer were optimized by using the one-factor experimental design and response surface analysis. The elemental composition and structure of the polymer suspension stabilizers were tested and analyzed by using X-ray spectroscopy (XPS), infrared spectroscopy (FTIR) and nuclear magnetic resonance hydrogen spectroscopy (H NMR). The hydrophobic aggregation behaviour of the polymer molecular chains was demonstrated from a microscopic point of view using fluorescence spectroscopy tests and size analysis of polymer molecular aggregates. Oscillation experiments on the isolation solution with suspension stabiliser showed that the hydrophobic groups contained in the polymers can undergo the effect of joining and bridging, and can also form a strong spatial network structure at 220°C, leading to the enhanced elasticity of the isolation fluid, which helps to alleviate the sedimentation of barite. Sedimentation stability and compatibility were evaluated for the isolation fluid containing suspension stabilizers. It was found that the isolation solution suspension performance is good under the condition of 90–220℃, its density difference is less than 0.10 g/cm3. It can also effectively prevent the contact contamination of the drilling fluid cement slurry, which is conducive to the improvement of the quality of the deep well cementing.

Strategies for alkali-free synthesis, surface modification, and electrophoretic deposition of composite films for biomedical applications

This investigation addresses increasing interest in composites for biomedical applications and advanced methods for their synthesis and electrophoretic deposition (EPD). The feasibility of preparation of hydroxyapatite (HA), titania and zirconia particles using branched polyethylenimine polymer (BPEI) or L-arginine amino acid as organic alkalizers is demonstrated. In this new approach, BPEI and L-arginine are used as alkalizers-capping agents instead of inorganic alkalis. The use of BPEI facilitates synthesis of HA nanorods with reduced size. This approach opens an avenue for the fabrication of nanoparticles of other functional inorganic materials using alkalizers-capping agents. It offers advantages of simple procedure, environmental benefits and improved control of particle size. Composite films are obtained by cathodic EPD using linear polyethylenimine (LPEI) as a charging and film-forming agent. A conceptually new approach is developed for anodic EPD of alginic acid polymer (AlgH) and composite films containing drug molecules in AlgH matrix. This strategy involves the use of L-arginine as an alkalizer for solubilization of drugs, which exhibit poor solubility in water. AlgH and drug molecules are solubilized in water and deposited by anodic EPD. Testing results confirm the fabrication of composite films, containing drug molecules. This method allows reduced gas evolution at the electrode, elimination of film porosity, improved stabilization of bioceramic particles in polymer solutions and facilitates composite film formation from stable suspensions. The deposition methods developed in this investigation can be used for deposition of other cationic and anionic polymers and their co-EPD with bioceramics, drugs and other functional materials.

Fast and efficient chromium(VI) extraction by colloidal Mg/Al layered double hydroxide nanoparticles

Due to the constraints associated with diffusion and mixing time, traditional kinetic and thermodynamic approaches were inadequate for probing the true mechanism of interaction between chromate and Layered Double Hydroxide (LDH). To circumvent these limitations, colloidal suspensions of Mg/Al-NO3 LDH, characterized by a positively charged surface (approximately +50 mV) in ultrapure water and a mean average diameter of 140 nm, allowing the formation of stable suspensions for days, were swiftly mixed with Cr(VI) suspensions at both pH = 4 and 9 using a stopped flow technique. This rapid mixing, accomplished in <5 milliseconds, enabled the examination of the initial stages of interaction between the toxic anion and the host compound. Two distinct steps in the adsorption process were identified: a very fast step (completed in <5 ms), representing up to 80% of the measured variation, and a slower step lasting up to 100 s. The fast step assumed to be driven by electrostatic interaction (ζ ∼ +50 mV) with the surface, and sites close to the surface are easily accessible to the chromate anions. The slower step corresponded to a diffusion process close or inside the particles. Chromate extraction efficiency was investigated through ultrafiltration tests, varying the LDH and chromate amounts, indicating that 2 nitrate ions are exchanged for 1 chromate, regardless of the pH considered, and a total exchange can be fulfilled with 0.1 g L−1 of LDH within the explored concentration range.

Biosurfactants as stabilizers of niclosamide nanocrystals: Enhancing stability, solubility, and cytotoxicity profiling

Biosurfactants are surface-active compounds of biological origin, stable over a wide range of temperature, pH, and salinity. In this work, the ability of the biosurfactants rhamnolipid (RAM), sophorolipid (SOFO) and surfactin (SURF) to stabilize a nanocrystal suspension of niclosamide (NCL) in water, and to enhance the drug solubility were evaluated. The performances were compared with those of the synthetic surfactants tween 80 (TW) and soluplus (SOLU). Overall, RAM, SOFO, and SURF proved to be as effective as TW and SOFO in terms of NCL nanocrystal suspension stabilization. Formulations containing 3 % (w/w) surfactant exhibited the best stability at 4 °C and 25 °C. The three biosurfactants also led to an improvement of aqueous NCL solubility, even when a slurry of the micronized drug was used without nanocrystal formulation. The best performance was observed for the SURF 3 % (w/w) nanocrystal formulation (1157.48 μg/mL), which released more than twice the amount of NCL compared to the best synthetic surfactant formulation (TW 3 % (w/w), 542.57 μg/mL), and 622 times more than the pure solid drug (1.86 μg/mL). Cell viability was not compromised by the surfactants alone, indicating that the formulation cytotoxic effect is related to the enhanced solubilization of NCL. Consistently, the NCL/SURF formulation was the most effective, achieving a maximum cytotoxicity effect of 80 % at a concentration of 1000 nM, while the other formulations reached a maximum effect of 71 % at concentrations starting from 1500 nM. Nevertheless, when the balance between formulation stability, drug release enhancement, and cytotoxicity is considered the three biosurfactants studied in this work showed significant potential advantages relative to synthetic analogues that can be explored in pharmaceutical development.

Unveiling the synergistic interaction: Investigating the enhanced mechanism of 4H–SiC chemical mechanical polishing with the addition of sodium silicate and manganese dioxide

Silicon carbide (SiC), the quintessential semiconductor material, poses an acute challenge to the realization of highly efficient ultra-precision processing. This study has investigated the effect of the combined ratio of sodium silicate and manganese dioxide on the polishing rate and surface roughness of 4H–SiC in chemical mechanical polishing (CMP). The synergistic mechanism of sodium silicate and manganese dioxide on slurry spreading performance and particle dispersion stability is characterized by surface wettability, surface tension, scanning electron microscopy, zeta potential analysis and X-ray photoelectron spectroscopic. Based on the above studies, the synergistic mechanism of sodium silicate and manganese dioxide on the CMP of 4H–SiC is attributed to the improvement of the suspension stability of the abrasive as well as the oxidizing ability of the slurry.

VMT/ACP/Dextran composite nanosheets against dental caries through promoting mineralization of dentin tubules, pH buffering, and antibacterial

Dental caries is a worldwide public healthcare concern, and is closely related to the acidic environment that caused by bacterial decomposition of food. In this study, a two-step ion exchange liquid-phase stripping method was applied to strip out vermiculite (VMT) nanosheets, then amorphous calcium phosphate (ACP) and dextran were inserted between the VMT nanosheets interlayer to obtain a composite two-dimension nanosheets (VMT/ACP/Dextran). VMT/ACP/Dextran composite nanosheets exhibited excellent biocompatibility and could provide exogenous Ca2+and PO43− from ACP, provide SiO44−, Mg2+, Fe2+ and obtain buffering pH and antibacterial properties from VMT, as well as improve suspension stability and targeting Streptococcus mutans through glucan. The in vitro study showed that the composite materials could promote the mineralization and sealing of dentin tubules by releasing active ions, buffer pH 4.5 (a value close to the pH in the dental plaque environment) to pH 6.6–7.1 (values close to the pH in human saliva) through ion exchange, and exert antibacterial effects by targeting Streptococcus mutans and exerting oxidase like and peroxidase like activities to produce reactive oxygen species (ROS). The in vivo animal study showed that daily cleaning teeth using VMT/ACP/Dextran composite nanosheets could effectively reduce the incidence rate and severity of dental caries in rats. Taking together, the developed VMT/ACP/Dextran composite nanosheets, which integrated the excellent properties of VMT, ACP and dextran, can effectively prevent dental caries through a combination of factors such as buffering acids, antibacterial properties, and promoting calcification, and may be used as an active ingredient for daily oral hygiene or filling materials to prevent and treat dental caries.

(Invited) Sequential Development of Continuous Electro-Osmotic Dewatering for Phosphatic Clay Suspensions

The beneficiation plant associated with a typical Florida phosphate mining operation produces more than 6,300 L/s of a dilute 2-3 wt.% suspension of phosphatic clay. The clay-water suspension is pumped into large impoundments called clay settling areas in which partial separation is achieved by hindered settling and self-consolidation. As clay settles, the supernatant water is recycled for use in the beneficiation plant. A top crust is formed after a few years, but the clay beneath the crust has a large water content and a pseudo-plastic character that limits the amount of weight the settling area can support. Clay settling areas cover roughly 390 square kilometers of land in Florida. Uses for the land are limited by the properties of the clay that leave the settling areas unstable, even after 50 years of elapsed time. In addition, failure of the impoundments has caused major releases into local rivers.1 Research in use of electrokinetic phenomena to accelerate the dewatering process of phosphatic clay has been active for more than 50 years.2,3 The use of an electric field to separate the water from the solids is attractive because the inherent stability of the clay suspension is due, in part, to the surface charges residing on the platelets. This presentation will describe the results of a 7-year research project, funded by Mosaic, to create an electrokinetic alternative to the creation of clay settling areas. Through a systematic development of prototypes, from batch4,5 to semi-continuous with emphasis on water clarification6 to semi-continuous with emphasis on solids extraction, our team has developed a fully continuous prototype using electrokinetic dewatering. The fully continuous prototype itself underwent several prototype designs, culminating in a single-stage design for continuous electro-osmotic dewatering of phosphatic clay suspensions that demonstrated efficient production of a dewatered cake with a solids content of 35 wt.% at a dry-clay production rate of 4.5 kg/h m2 from a feed clay of 10 wt.%.7,8 The results were supported by measurements of yield stress and a mathematical model that accounted for compressibility of the cake and for both electro-osmotic and hydraulic permeability.9 Patents were published that correspond to the above stages of development.10-12 References Damage Cases and Environmental Releases from Mines and Mineral Processing Sites, U.S. Environmental Protection Agency, Washington, DC, 1997.A. Dizon and M. E. Orazem, “Advances and Challenges of Electrokinetic Dewatering of Clays and Soils,” Current Opinion in Electrochemistry, 22 (2020), 17-24.J. Q. Shang and K. Y. Lo, “Electrokinetic Dewatering of a Phosphate Clay,” Journal of Hazardous Materials, 55 (1997), 117-133J. P. McKinney and M. E. Orazem, “A Constitutive Relationship for Electrokinetic Dewatering of Phosphatic Clay Slurries,” Minerals & Metallurgical Processing, 28 (2011), 49-54.J. P. McKinney and M. E. Orazem, “Electrokinetic Dewatering Phosphatic Clay Settling Areas: Numerical Simulation and Economic Assessment,” Minerals & Metallurgical Processing, 28 (2011), 71-76.R. Kong and M. E. Orazem, “Semicontinuous Electrokinetic Dewatering of Phosphatic Clay Suspensions,” Electrochimica Acta, 140 (2014), 438-446.R. Kong, A. Dizon, S. Moghaddam, and M. E. Orazem, “Development of Fully-Continuous Electrokinetic Dewatering of Phosphatic Clay Suspensions,” in Electrochemical Engineering: From Discovery to Product, Volume XVIII of Advances in Electrochemical Science and Engineering, R. Alkire, P. N. Bartlett, and M. Koper, editors, John Wiley & Sons, Hoboken, 2018, 159-192.A. Dizon and M. E. Orazem, “Efficient Continuous Electrokinetic Dewatering of Phosphatic Clay Suspensions,” Electrochimica Acta, 298 (2018), 134-141.A. Dizon and M. E. Orazem, “Mathematical Model and Optimization of Continuous Electro-Osmotic Dewatering,” Electrochimica Acta, 304 (2019) 42-53.M. E. Orazem and R. Kong, “Electrokinetic Dewatering of Phosphatic Clay Suspensions,” U.S. Patent No. 10,486,108 B2, Issued: November 22, 2019.M. E. Orazem, R. Kong, S. Moghaddam, H. Lai, D. Yu, Y. Huang, and D. Bloomquist, “Continuous Electrokinetic Dewatering of Phosphatic Clay Suspensions,” U.S. Patent No. 10,315,165 B2, Issued: June 11, 2019.M. E. Orazem and A. R. Dizon, “Device for Efficient Continuous Electrokinetic Dewatering of Phosphatic Clay Suspensions,” U.S. Patent No. 11,208,342 B2, Issued: Dec. 28, 2021.

Enzyme Engineering to Produce SWCNT Nanosensors as a Generalizable Platform for Biochemical Imaging and Sensing

Single-walled carbon nanotubes (SWCNT) stand out as attractive candidates for near-infrared (nIR) fluorescent imaging and chemical sensing. However, to render SWCNT chemically-selective, rational design of the surface corona is required to achieve sufficient sensitivity and selectivity to the target analyte. Recently, we reported on a facile sonication-based generation of glucose oxidase (GOx)-SWCNT conjugate for glucose detection [1]. Notably, we found that the analyte response mechanism does not involve catalytic oxidation of glucose, which motivated us to develop nanosensors using catalytically inactive GOx for enhanced reversibility and biocompatibility. In this study, we study the generalizability of our approach in producing SWCNT-based nanosensors based on 1- facile direct probe tip sonication, and 2- with engineered enzymes, showing the potential applicability of the sonication-based approach as a generalizable strategy for generating rationally designed nanosensors capable of detecting and imaging various analytically-relevant biomolecules.In this work, to test the generalizability of generating enzyme-SWCNT nanosensors, we generated conjugates by facile direct sonication of SWCNT with following enzymes: GOx, choline oxidase (ChOx), horseradish peroxidase (HRP), acetylcholineesterase, tyrosinase, cholesterol oxidase (CholOx), lactate oxidase, alcohol oxidase, xanthine oxidase, and galactose oxidase. Remarkably, six out of nine enzymes yielded stable suspensions of enzyme-SWCNT conjugates following probe-tip sonication, all of which successfully worked as nanosensors to detect their corresponding analytes. These nanosensors, in particular HRP-SWCNT and CholOx-SWCNT, exhibited excellent responses to their targets, with a maximum ΔF/F 0 of up to 300 % and 100 %, respectively. H2O2 is known to quench SWCNT fluorescence, and H2O2 nanosensors previously developed with SWCNT exhibited a negative fluorescence modulation as the sensor output with some challenges towards nanosensor selectivity. We highlight that our approach enables HRP-SWCNT nanosensor generation, which provides a strong ΔF/F 0 = 300 % and instantaneous turn-on response towards H2O2 within 2 s. Next, we sought to show that enzyme inactivation can produce SWCNT-based nanosensors that detect analytes without analyte consumption. To do so, we use ChOx as a model system to show that recombinant enzymes can be used as a generalizable approach to generating catalytically-inactive nanosensors. As expected, nanosensors prepared with mutant-ChOx exhibited responses comparable to those prepared with native ChOx, but without consuming the analyte or producing toxic byproducts such as H2O2. Thus, sonication-based physisorption of engineered enzymes to SWCNTs holds the potential to facilitate rapid nanosensor generation capable of detecting various biologically relevant molecules with reversibility and biocompatibility, thereby motivating their use in in vivo applications.[1] Nishitani, S., Tran, T., Puglise, A., Yang, S. & Landry, M. Engineered Glucose Oxidase-Carbon Nanotube Conjugates for Tissue-Translatable Glucose Nanosensors. Angew. Chem. Int. Ed Engl. e202311476 (2023)

Structural Analysis of Cathode Slurry Under Flow Using New Probe for Rheo-Impedance Measurements

A battery slurry will experience a variety of shear stresses as it goes through the manufacturing process. The full characterization of a slurry for quality control is challenging due to the complex and changing relationship between active material particles, binder, and the carbon black conductive network as a function of these different shear environments. Rheology is a powerful tool for measuring suspension stability and the viscosity at different shear stresses. However, it cannot characterize the structure of the carbon black conductive network because the rheological properties are dominated by the larger active material particles. Poor distribution or aggregation of the carbon black additive will create an electrode with higher electrical resistance, resulting in more heat generation and a shorter cycle life. Electrochemical impedance spectroscopy is an information dense technique that probes the sample using an alternating current or potential at a range of frequencies. Amongst its many applications, EIS can discriminate between simultaneous events that take place over different time scales, such as the measurement of conductivity within a solid electrode vs the ionic conductivity of the electrolyte. Combining these techniques into a simultaneous measurement will characterize the rheological behavior and the structure of the carbon black conductive network under flow and temperature conditions that are relevant for a manufacturing environment. A novel probe for the simultaneous measurement of rheological properties and electrochemical impedance spectroscopy (Rheo-EIS) is herein presented. A structural analysis of Li-ion battery cathode slurries and carbon paste is used to demonstrate the technique.

Microbial assisted date palm nanocellulose isolation and the fabrication of hydrophobic bioaerogel for oil absorption application

This study introduces a novel approach by utilizing Aspergillus niger for the isolation of nanocellulose from date palm sheath fibers (DPSF), achieving significant nano-scale reduction and high yield efficiency. The enzymatic breakdown by Aspergillus niger efficiently reduced the fibers' size, achieving an 81.3 % transition to nano-scale (<100 nm) after 96 hours, with an impressive 84 % yield using 72 hours of fungal treatment. The isolated nanocellulose demonstrated superior thermal stability and zeta potential value of −32.5 mV indicates a stable colloidal suspension due to the electrostatic repulsion between nanocellulose particles. Triethoxymethylsilane (TEMS) modification of nanocellulose aerogel significantly improved mechanical strength from 0.0194 to 0.03614 N/mm². Treatment with 5 % TEMS reduced water absorption from 41.7 g/g to 11.3 g/g, enhancing hydrophobicity (water contact angle 136.21°) and shifting material preference away from water. TEMS-treated samples showed increased absorption capacities of up to 44.3 g/g for cooking oil and 57.6 g/g for motor oil, highlighting improved compatibility with non-polar substances. These advancements underscore a sustainable solution for oil spill remediation, offering significant potential in environmental conservation and recovery efforts.

Biochar/Biopolymer Composites for Potential In Situ Groundwater Remediation.

This study explores the use of pine wood biochar (BC) waste gasified at 950 °C as fillers in polymer matrices to create BC@biopolymer composites with perspectives in groundwater remediation. Four biochar samples underwent different sieving and grinding processes and were extensively characterized via UV-Vis, FTIR, and FESEM-EDS, highlighting the fact that that BCs are essentially graphitic in nature with a sponge-like morphology. The grinding process influences the particle size, reducing the specific surface area by about 30% (evaluated by BET). The adsorption performances of raw BC were validated via an adsorption isotherm using trichloroethylene (TCE) as a model contaminant. A selected BC sample was used to produce hydrophilic, stable polymer composites with chitosan (CS), alginate (ALG), potato starch (PST), and sodium carboxymethylcellulose (CMC) via a simple blending approach. Pilot sedimentation tests over 7 days in water identified BC@PST and BC@CMC as the most stable suspensions due to a combination of both hydrogen bonds and physical entrapment, as studied by FTIR. BC@CMC showed optimal distribution and retention properties without clogging in breakthrough tests. The study concludes that biopolymer-based biochar composites with improved stability in aqueous environments hold significant promise for addressing various groundwater pollution challenges.

Physicochemical characteristics of highly concentrated suspensions with some types of Ukrainian coal

ABSTRACT The investigation results of granulometric composition, zeta potential, sedimentation stability, and viscosity of some water-coal suspensions made of Ukrainian coal from the “Stepova” mine, Lviv-Volyn region, are reported. The most effective granulometric composition of the water-coal suspension consisting of the rough and fine fractions is found from the analysis of the abovementioned physicochemical characteristics of the suspensions. Based on the complex investigation of the zeta potential of the dispersed phase particles, viscosity, and sedimentation stability of the suspensions, it was established that the best technological effectiveness can be expected for the suspensions containing 60% of the rough fraction (sized between 100 and 250 µm) and fine particles sized between 20 and 40 µm. In such systems, the particles form a quasi-stable structure, where the lower-charged small particles are located in the interparticle space between the highly charged bigger particles. All particles bear the same charge, increasing the system’s sedimentation stability and avoiding decomposition for at least 5 days. This time seems reasonable for the preparation, storage, and pumping of the suspensions while their viscosity and stability meet the relevant technological requirements.