Increasing Solution Concentration Research Articles

Investigation on the mechanical properties of Bacillus subtilis self-healing concrete

In the process of research and development of self-healing concrete, it is observed that there are three main factors controlling the self-healing effect of concrete: first, the bacteria with repair ability and strong vitality; Second, the carrying capacity of the carrier and the matching degree with concrete; The third is the concentration of bacteria. This paper focuses on the mechanical properties of Bacillus subtilis self-healing concrete with sisal fiber, PVA, and expanded perlite as the carrier. To better study the mechanical properties of self-healing concrete caused by the carrier, the experiment adopts the design parameters of C30 concrete and conducts experiments on compressive resistance, flexural resistance, freeze-thaw cycle, and sulfate corrosion resistance to analyze the influence of different carriers on the mechanical properties of self-healing concrete, and obtains the best carrier. The concentration gradients of three groups of bacterial solution were set as 2od, 2.5od, and 3od, respectively, for comparison to avoid the influence of bacterial concentration. It compared the impact of bacterial solution concentrations on the specimen's mechanical properties, and the effect of carriers was also analyzed. The experimental results show that the mechanical properties of the specimen using 2.5od bacterial liquid concentration with PVA as the carrier have peaked. With the increase in bacterial solution concentration, the specimens' comprehensive mechanical properties increased first and then decreased. The compression resistance of the specimen with PVA is higher than that of the specimen with sisal fiber and expanded perlite. At the same time, the frost resistance and corrosion resistance of the PVA carrier specimen is also higher than that of the specimen with sisal fiber and expanded perlite carrier.

Coupled model for electro‐osmosis consolidation and ion transport considering chemical osmosis in saturated clay soils

AbstractThe electro‐osmosis approach efficiently facilitates the rapid dewatering of soil with high water content and contributes to reducing contaminant levels within the clay soil. However, the changes of chemical field caused by ion transport in the clay soil during electro‐osmosis process will also influence the clay soil consolidation effect. Existing theories predominantly tend to disregard this crucial physical process and its resultant effects, thereby restraining a comprehensive analysis of electro‐osmosis consolidation (EOC) behavior under intricate chemical conditions. This study introduces a concise model of EOC and ion transport considering chemical osmosis. The model considers the nonlinear variation of clay soil parameters such as compressibility, permeability, and effective diffusion coefficients, along with the interaction between EOC and ion transport. Meanwhile, the correctness of the model is verified from different aspects such as theoretical derivation and model comparison. Based on the proposed model, the impacts of the variation in electrical field intensity and chemical concentration on the coupled behaviors between EOC and ion transport are systematically investigated, with and without incorporating nonlinear consolidation characteristics. The results show that diffusion and electro‐migration exhibit a more pronounced effect on ion transport during EOC. Simultaneously, with the increase of ion concentration in clay soil pore solution, the effects of chemical osmosis become increasingly apparent, thereby enhancing clay soil settlement.

Sulfate resistance of UHPC during dry-wet cycling and energy dissipation under compression

To study the sulfate resistance of ultra-high performance concrete (UHPC) in saline soil area of western China, four kinds of sulfate solution concentrations (0%, 5%, 10%, 15%) and 18 dry-wet cycle tests for 540 days were carried out on UHPC specimens. The effects of sulfate dry-wet cycles on the evolution of UHPC strength and energy were studied, the characteristic stress points during uniaxial compression of UHPC under sulfate dry-wet cycle were determined, based on the evolution law of each energy (total energy , dissipated energy , elastic stress ) at the characteristic stress points, the energy storage index was established to measure the damage degree of UHPC. The results show that the energy evolution process and damage mechanism of UHPC samples under sulphate-wet and dry cycle erosion are closely related to macro and micro changes. With the development of sulfate dry-wet cycle, the dissipative energy and elastic strain energy of UHPC at the characteristic stress points increased first and then decreased. The development trend of elastic strain energy and dissipative energy is more severe with the increase of sulfate solution concentration. The ratio of elastic strain energy at damage stress to elastic strain energy at peak stress () is taken as the energy storage index to measure the damage degree of UHPC, under 10%Na2SO4 erosion, can be increased by 21.41% at the highest and decreased by 29.67% at the lowest compared with the initial value. It shows that the damage process of UHPC is difficult and then easy, and this index can accurately reflect the external force required for the damage of UHPC under sulfate dry-wet cyclic erosion, and provide a reference for the safe and stable operation of UHPC in saline soil area.

Coupling of photovoltaic thermal with hybrid forward osmosis-membrane distillation: Energy and water production dynamic analysis

This study proposes a novel solar photovoltaic thermal (PVT)-driven forward osmosis (FO) and membrane distillation (MD) system for desalinating brackish water, addressing water scarcity issues by combining the advantages of FO's low operating cost with MD's ability to treat hypersaline water. A physics-based dynamic model was developed for the system, and the model equations were discretized and solved using an open-source algebraic modeling language. Model validation involved verifying the consistency of outputs between successive unit operations and conducting sensitivity analysis by varying one operating condition at a time. The analysis considered varying weather conditions while maintaining constant operating conditions. Increasing the flow rate of brackish water (cooling fluid) from 19.79 to 59.38 kg/h improved thermal efficiency by 28.7 %; however, FO and MD water fluxes decreased by 1.12 LMH and 7.77 kg/m2/h, respectively. Peak thermal efficiency (81.2 %) was achieved at the highest flow rate. Incorporating heat transfer analysis into FO models goes beyond the common focus on mass transfer, allowing for a more comprehensive understanding of energy dynamics within the system. Both FO and MD water fluxes improved with irradiance and ambient temperature but decreased with cooling fluid flow rate and wind velocity. Increasing feed concentration to 10,000 mg/l reduced water flux by 0.66 LMH, and for each 0.5 M increase in draw solution concentration, FO water flux increased by >10 LMH. Compared to MD water flux, FO water flux is more sensitive to changes in concentration than to changes in weather conditions.

Diffusiophoresis in Polymer and Nanoparticle Gradients.

Diffusiophoresis is the movement of the colloidal particles in response to a concentration gradient and can be observed for both electrolyte (e.g., salt) and nonelectrolyte (e.g., glucose) solutes. Here, we investigated the diffusiophoretic behavior of polystyrene (PS-carboxylate surface) microparticles in nonadsorbing charged and uncharged solute gradients [sodium polystyrenesulfonate (NaPSS), polyethylene glycol (PEG), and nanoscale colloidal silica (SiO2)] using a dead-end channel setup. We compared the diffusiophoretic motion in these gradient types with each other and to the case of using a monovalent salt gradient. In each of the nonadsorbing gradient systems (NaPSS, PEG, and SiO2 nanoparticles), the PS particles migrated toward the lower solute concentration. The exclusion distance values (from the initial position) of particles were recorded within the dead-end channel, and it was found that an increase in solute concentration increases exclusion from the main channel. In the polyelectrolyte case, the motion of PS microparticles was reduced by the addition of a background salt due to reduced electrostatic interaction, whereas it remained constant when using the neutral polymer. Particle diffusiophoresis in gradients of polyelectrolytes (charged macromolecules) is quite similar to the behavior when using a PEG gradient (uncharged macromolecule) in the presence of a background electrolyte. Moreover, we observed PS microparticles under different concentrations and molecular weights of PEG gradients. By combining the simulations, we estimated the exclusion length, which was previously proposed to be the order of the polymer radius. Furthermore, the movement of PS microparticles was analyzed in the gradient of silica nanoparticles. The exclusion distance was higher in silica nanoparticle gradients compared to similar-size PEG gradients because silica nanoparticles are charged. The diffusiophoretic transport of the PS microparticles could be simulated by considering the interaction between the PS microparticles and silica nanoparticles.

Numerical Simulation of Chemical Reactions’ Influence on Convective Heat Transfer in Hydrothermal Circulation Reaction Zones

Chemical reactions, mineral diffusion, and deposition are pivotal in understanding the mechanisms of mineral deposition and the formation of seafloor sulfides in the hydrothermal circulation process. To understand the formation process of anhydrite in submarine hydrothermal systems, a computational model that combined component transport and chemical reactions was established and simulated using the mass transport model. The deposition rate of calcium sulfate was defined, and the effects of factors such as porosity, ion concentration, and inflow velocity on the temperature field in the reaction zone were thoroughly investigated. The distribution of temperature, porosity, and velocity during the reaction process was obtained, allowing for the identification of the chemical reaction patterns of certain ions in the early stages of hydrothermal activity. The simulation revealed the occurrence of biochemical reactions between two types of ions, leading to their deposition on the solid framework of a porous medium. With the increase in inflow velocity and solute concentration, the average porosities of the porous medium decreased by 0.495% and 0.468%, respectively, which consequently altered the structure of the rock. Such findings contribute to the inference of formation and extinction mechanisms of seafloor crusts and hydrothermal chimneys.

Effect of Electrospinning Parameters on the Morphological and Thermal Properties of ABS/ENR Electrospun Fibres

The electrospun of the Acrylonitrile-butadiene-styrene (ABS) blend with epoxidized natural rubber (ENR) is fabricated using the electrospinning technique. Research shows that ABS/ENR electrospun fibres have not been studied. The effects of electrospinning parameters were investigated to determine a significant effect on the microstructure, surface roughness, fibre diameter, and fibre distribution of the electrospun membranes. Sample preparation is made straightforwardly by dissolving ABS and ENR in acetone solvent using a magnetic stirrer. In this research, there are two solution parameters being studied: the ABS/ENR solution concentration (15 to 25 wt.%) and the ratio of ENR (100:0, 70:30, 50:50). Meanwhile, process parameters that are being studied are applied voltage (15 kV to 30 kV) and distance from syringe tip to collector (5cm to 15cm). FTIR results showed that hydrogen bond interaction occurs between ABS and ENR. According to the SEM images, micrometre and sub-micrometre fibres with a smooth surface and bead formation were produced at a concentration of 25%, a ratio of 70:30, a voltage of 30kV, and a distance of 15cm. The diameter of electrospun fibres increases with increasing solution concentration, ranging from 400 nm to 4.5 µm. The diameter of the electrospun fibres decreased with the addition of ENR, increasing voltage, and tip-to-collector distance. TGA results showed that ABS/ENR blends gave higher degradation temperature (393.7°C) than pure ABS (368.8°C), which enhanced thermal stability.

Enhanced heavy metal adsorption capacity of surface-functionalized Philippine natural zeolite in simulated wastewater

The adsorption efficiency of surface-functionalized Philippine natural zeolite (PNZ) for heavy metal uptake from single and mixed metal ion-simulated wastewater solution is reported in this work. Atomic adsorption spectroscopy (AAS) findings revealed that NaCl-modified PNZ (MPNZ) exhibited the highest zinc ion adsorption of 99.96 % while PNZ yielded an adsorption of 95.61 %. The adsorption isotherms of raw PNZ and MPNZ both show similar shapes that reflect Type IV adsorption-desorption isotherms with Type H2 hysteresis loop which can be observed for micro-mesoporous materials (pore containing 2–50 nm). An increase in PNZ pore size from 10.11 nm to 13.36 nm for NaCl-PNZ and 15.59 for NaOH-PNZ is observed after alkaline treatment. EDS confirmed the decrease in Si/Al ratio from 4.02 to 3.76, indicative of possible higher negative charge in the PNZ framework which is favorable for an enhanced Coulombic or electrostatic interaction with the cationic heavy metals being detected in this study. MPNZ demonstrated an adsorption capacity of 99.96 % for copper in mixed-ion solution while 88.49 % and 86.67 % were obtained for zinc and nickel, respectively. These values are higher compared to PNZ having only 32.21 % uptake for zinc and 38.00 % for nickel. A hierarchy of the average metal adsorption capacity showed the order: copper > nickel > zinc. Rapid adsorption at the first hour of the adsorption reaction was attained in all solutions while samples with pH 9 exhibited the highest Ni2+ and Zn2+ percent removal. Moreover, the increase in initial solution concentration led to lower adsorption efficiency and the maximum uptake was attained at 100 ppm. The equilibrium data of adsorption and mechanism were suitably described by Langmuir isotherm model. With these, surface functionalization of PNZ has further enhanced its cationic adsorption capacity on heavy metals in both single and mixed-ion solution having promising potential for wastewater remediation.

Mathematical modeling of the transport characteristics of a PVDF-based cation-exchange membrane with low water content

New effective ion-exchange membranes are needed for a variety of applications, with a particularly pressing need for membranes used in fuel cells and membrane water electrolysis. PVDF-based membranes are promising for these and other applications. Two samples of such membranes with a low water content are studied. The interest in the behavior of these samples is that with an increase in the bathing NaCl solution concentration, the diffusion permeability decreases, whereas usually it increases along with increasing membrane conductivity. The hypothesis is that with increasing concentration, the water content decreases even more, which leads to a narrowing of the intercluster ion-conducting channels and a reduction in the effective mobility of coions, since the latter have to go around narrowed sections of channels. To simulate the concentration dependence of conductivity, diffusion permeability and transport numbers for the two above samples, the microheterogeneous model is extended to describe the loss of water with increasing external concentration and take into account the decrease of coion percolation through the membrane. The results of simulation are compared with the experimental data.

Experimental study of the dynamics and mass transfer of single CO2 bubble accompanied by reactions in Hele-Shaw cell

The reduction of carbon emissions has become a critical global issue, and the use of monoethanolamine (MEA) solution for CO2 absorption is prevalent in industry. To elucidate the mass transfer mechanisms in reactive multiphase flow, we employed high-speed photography and digital image processing to examine the dynamics and mass transfer behavior of CO2 bubbles in a Hele-Shaw cell. The results indicate that as the MEA solution concentration increases, oscillations during bubble ascent diminish, and the terminal velocity decreases. Based on changes in the mass transfer coefficient, the reaction process can be segmented into a phase of intensified mass transfer, marked by a rapid decrease in bubble equivalent diameter, and a phase of deteriorating mass transfer, where the diameter stabilizes. Additionally, we introduced a dimensionless mathematical model for the Sherwood number based on experimental findings, and its reliability was confirmed.

Capillary Imbibition Laws of Fresh–Brackish Waters in Sandstone

Understanding the capillary imbibition laws of brackish water in rocks is necessary to reveal the mechanism of fluid, salt, and ion transport. In this study, we investigated the capillary imbibition laws of a Na2SO4 solution of different concentrations in sandstone by measuring the parameters of water absorption mass, water migration front height, nuclear magnetic resonance (NMR) T2 spectra, and stratified moisture distribution. The results indicate the following: (1) With an increase in the salt solution concentration, the water absorption rate of samples increases, specifically manifested in an increase in the rate of absorption mass and a rising rate of the absorption front. (2) With an increase in the salt solution concentration, the total NMR signals in samples measured at the end of water absorption decreases; that is, the total amount of water absorption decreases. (3) When the solution concentration exceeds 0.50 g/L, variations in the NMR signal of samples and the absorbed water mass over time are not synchronic and are even opposite at some stages. Based on the capillary dynamic theories of liquid, the influence of salts on solution properties and the modification of the pore structure by crystallization are considered when discussing the underlying mechanism of capillary imbibition in sandstone. By calculating the physical properties such as the density, viscosity, surface tension, and contact angle of solutions with different concentrations, the imbibition process does not exhibit any significant variation with the difference in the properties of the liquid. The equivalent capillary radii of the samples at varying salt concentrations are obtained by fitting the capillary dynamics curves with the theoretically calculated values. The equivalent capillary radii of samples in higher salt concentrations are larger, i.e., the difference in capillary imbibition laws introduced by the salt concentration should be attributed to modifications to the pore structure caused by salt crystallization.

Creep deformation behavior and microstructure of α-Mg/long-period stacking ordered (LPSO) duplex Mg-Y-Zn alloy prepared by hot extrusion and heat treatment

There exists a great demand for improving the creep resistance of α-Mg/long-period stacking ordered (LPSO) duplex alloys. In this study, microstructure control through hot extrusion and heat treatment was employed on Mg-Y-Zn duplex alloys with the aim of achieving superior creep resistance. The extruded Mg-Y-Zn alloy exhibited an enhancement in the creep resistance with increasing heat treatment temperature. Furthermore, the heat-treated samples demonstrated outstanding creep resistance even under high stress. Their creep behavior is characterized by a low minimum creep rate and a relatively small stress exponent (n ∼ 5) even at high stress. Microstructural observations revealed that heat treatment induces grain coarsening and an increase in solute concentration within the recrystallized grains. Additionally, during creep deformation, a plate-like LPSO phase and kink bands formed within the recrystallized grains. Therefore, it is affirmed that the exceptional creep resistance observed in the Mg-Y-Zn alloys in this study can be attributed to the microstructure evolution induced by heat treatment and creep deformation.

Analysing the Photo-Physical Properties of Liquid Crystals

Intrinsically fluorescent liquid crystals are highly sought after for a variety of applications. Most of the measurements of photo-physical properties of liquid crystals are made in dilute solutions, which is mainly due to the relative ease of both these measurements and the interpretation of data. The fluorescence spectra depend on a number of parameters including the concentration in liquid crystal solutions, the device geometry, and the mesophase in which the spectra have been measured. Working with neat, or concentrated, liquid crystal samples adds experimental complexities such as the inner filter effect (IFE), which affects the collection of data, interpretation of the results, and accuracy of the conclusions. In this paper, we present a systematic study of the photo-physical properties of both a model reference material, Nile red, and a nematic liquid crystal, 4-cyano-4′-pentylbiphenyl (5CB). The influence on the emission spectra of an increasing solute concentration is investigated and discussed. Moreover, a detailed investigation of the influence of the used device geometry, as well as the choice of appropriate data fitting methodologies, are presented.

The Factors Influencing Lithium Carbonate Crystallization in Spent Lithium-Ion Battery Leachate

In this study, lithium was recovered from spent lithium-ion batteries through the crystallization of lithium carbonate. The influence of different process parameters on lithium carbonate precipitation was investigated. The results indicate that under the conditions of 90 °C and 400 rpm, a 2.0 mol/L sodium carbonate solution was added at a rate of 2.5 mL/min to a 2.5 mol/L lithium chloride solution, yielding lithium carbonate with a recovery rate of 85.72% and a purity of 98.19%. The stirring rate and LiCl solution concentration significantly impact the particle size of lithium carbonate aggregates. As the stirring rate increases from 200 to 800 rpm, the average particle size decreases from 168.694 μm to 115.702 μm. Conversely, an increase in the LiCl solution concentration reduces the lithium carbonate particle size, with an average particle size of only 97.535 μm being observed at a LiCl solution concentration of 2.5 mol/L. It was also observed that nickel and cobalt ions become incorporated into the crystal lattice of lithium carbonate, thereby affecting the growth and morphology of lithium carbonate.

Modeling and analysis of the triple diffusion unsteady flow of couple stress nanofluid with variable viscosity and distinct thermal sources

Thanks to their optimal thermal characteristics, nanomaterials stand out for their varied applications in heat transfer systems, energy storage, industrial processes, and biomedical research. Recently, scientists explored various dynamic properties in nanofluid flow to develop an even better thermal model. In this context, the phenomenon of triple diffusion in nanofluids constitutes an active area of research, offering promising applications in nanotechnology, metallurgical processes, chemical reactors, and thermo-diffusion processes. This paper analyzes the triple diffusion flow of a torque-constrained nanofluid, induced by a periodically oscillating porous surface, taking into account the importance of variations in thermal consequences. The viscosity of the torque-constrained nanofluid is assumed to be temperature-dependent. The analysis takes into account the variable role of thermal conductivity, mass diffusivity, and solute volume fraction. The modeling of the problem is expressed by coupled nonlinear partial differential equations. The semi-analytic technique, known as the homotopic analysis scheme, is used for resolution. The solution is validated and confirms the convergence region. The physical aspects of the parameters are examined with regard to the parameters involved. The simulated observations reveal that with the Dufour–Lewis factor and varying mass diffusivity, an increase in solute concentration is seen. The concentration of nanoparticles decreases with the nano-Lewis number.

An Artificial Gut/Absorption Simulator: Understanding the Impact of Absorption on In Vitro Dissolution, Speciation, and Precipitation of Amorphous Solid Dispersions.

Upon dissolution, amorphous solid dispersions (ASDs) of poorly water-soluble compounds can generate supersaturated solutions consisting of bound and free drug species that are in dynamic equilibrium with each other. Only free drug is available for absorption. Drug species bound to bile micelles, polymer excipients, and amorphous and crystalline precipitate can reduce the drug solute's activity to permeate, but they can also serve as reservoirs to replenish free drug in solution lost to absorption. However, with multiple processes of dissolution, absorption, and speciation occurring simultaneously, it may become challenging to understand which processes lead to an increase or decrease in drug solution concentration. Closed, nonsink dissolution testing methods used routinely, in the absence of drug removal, allow only for static equilibrium to exist and obscure the impact of each drug species on absorption. An artificial gut simulator (AGS) introduced recently consists of a hollow fiber-based absorption module and allows mass transfer of the drug from the dissolution media at a physiological rate after tuning the operating parameters. In the present work, ASDs of varying drug loadings were prepared with a BCS-II model compound, ketoconazole (KTZ), and hypromellose acetate succinate (HPMCAS) polymer. Simultaneous dissolution and absorption testing of the ASDs was conducted with the AGS, and simple analytical techniques were utilized to elucidate the impact of bound drug species on absorption. In all cases, a lower amount of crystalline precipitate was formed in the presence of absorption relative to the nonsink dissolution "control". However, formation of HPMCAS-bound drug species and crystalline precipitate significantly reduced KTZ absorption. Moreover, at high drug loading, inclusion of an absorption module was shown to enhance ASD dissolution. The rank ordering of the ASDs with respect to dissolution was significantly different when nonsink dissolution versus AGS was used, and this discrepancy could be mechanistically elucidated by understanding drug dissolution and speciation in the presence of absorption.

Symmetry of Pyridine Derivatives Controlled Two-Dimensional Nanostructural Diversity by Co-Assembly with Aromatic Carboxylic Acids.

The self-assembly behaviors of aromatic carboxylic acids are commonly investigated at the liquid/solid interfaces because of their rigid skeletons and both hydrogen-bond donors and receptors. However, self-assemblies of aromatic carboxylic acids with low symmetry and interactions between carboxylic acid and pyridine derivatives are worth exploring. In this work, the self-assembled structural transitions of a kind of low-symmetric aromatic carboxylic acid (H4QDA) are regulated by the coadsorption of two pyridine derivatives (DPE and T4PT) with different symmetry, which are investigated by scanning tunneling microscopy under ambient conditions. For the H4QDA/DPE system, the grid structure appears. For the H4QDA/T4PT system, the coassembled morphologies display an obvious concentration dependence. With the increase of solution concentration of T4PT, three coassembled patterns (network structure, chiral linear structure, and brick-like structure) are observed. Corresponding structural models suggest that the O-H···N hydrogen bonds have great contributions to stabilizing these coassembled structures. Our studies will help to explore the complexity, diversity, and functionality of multiple component systems and are conducive to further understanding the underlying mechanisms in the assembly process.

Corrosion behavior of Ti-based bulk amorphous alloys in acidic solutions

The corrosion behavior of the Ti34.3Zr31.5Cu5Ni5.5Be23.7 bulk amorphous alloy was investigated in different concentrations of the HCl and H2SO4 solutions. Electrochemical testing and scanning electron microscopy analysis indicate that Cl− ions can cause pitting damage in the HCl solution during the polarization process, and the pitting potential decreases with increasing solution concentration. The degree of damage to the corroded surface is positively correlated with the solution concentration. A passive film forms in the H2SO4 solution, indicating good corrosion resistance. X-ray photoelectron spectroscopy shows that the stability of the passivated film decreases with increasing HCl solution concentration. The corrosion rates of the four materials were obtained by an immersion experiment in HCl solution. The results reveal that Ti34.3Zr31.5Cu5Ni5.5Be23.7 bulk amorphous alloy has the best corrosion resistance, with a corrosion rate of 7.22×10−3 mm/a, which is approximately 1/1294 that of 316L stainless steel.

Study on the preparation of porous polyethylene glycol terephthalate film and the influencing factors of etching rate

AbstractPorous polyethylene glycol terephthalate (PET) film is a kind of mesopore structure template with pore size ranging from nanometer to micrometer by chemical etching after irradiation of heavy ions. The etching rate is an important factor affecting the pore morphology and quality of the membrane. In this paper, four stacked PET film were irradiated with 140 MeV 32S ions at room temperature and vacuum. During chemical etching of irradiated samples, the path etching rate Vt was determined by conduction method, and the bulk etching rate Vb was determined by weighing method. The relationship between etching temperature, concentration, sensitization time, and etching rate was studied. The results show that the etching rate is exponentially correlated with the etching temperature, and increases linearly with the increase of the etching solution concentration. When the concentration of NaOH is 3 mol·L−1 and the etching temperature is 75°C, the formation of cylindrical micropores is the most favorable. The pore size of porous PET film can be adjusted, and the relationship between pore size and etching time is . This is of great significance for the preparation of nanowires with uniform size and stable properties.Highlights We have obtained the optimal conditions for obtaining cylindrical holes. The relationship between the diameter of holes and etching time were determined.

Local deposition characteristics of calcium carbonate fouling in different enhanced tubes

With the development and advancements of modern industry, the application of enhanced tubes is becoming more and more extensive in various engineering domains and technological applications. When water is used as the working fluid for thermal energy utilization, there is a large chance of accumulating a large amount of fouling on the surface of the enhanced tubes. This paper establishes a mathematical model of the local fouling deposition of calcium carbonate in enhanced tubes. The model is used to simulate and compare the local fouling characteristics of CaCO3 in different tubes. In addition, a study is conducted on the effects of different inlet flow rates, water temperature, and calcium carbonate concentrations on the local fouling resistance of bellows tubes. The results showed that the local fouling resistance (average) and local fouling resistance of enhanced tubes is smaller than that of circular tubes. Additionally, the bellows tubes yielded the best scale inhibition effect. The obtained local fouling resistance is also found to change periodically along the length of the tube. The local fouling resistance decrease with an increase in the inlet flow rate and wall temperature, and increases with an increase in the calcium carbonate solution concentration.