Increasing MgCl2 Concentration Research Articles

CO2 sequestration by wet carbonated magnesium slag with high-content aragonite whiskers for improving cement performance as underground filling material

Magnesium slag (MS) is an alkaline waste residue from magnesium smelting processes. This study aimed to utilize the magnesium oxide in MS and adopt MgCl2 as the calcium carbonate crystal modifier to prepare high length-to-diameter ratio aragonite whiskers via wet carbonation, which can achieve high-value recovery of MS while capturing CO2 and enhancing cement as underground filling material. The effects of MgCl2 concentration on the carbonation process, composition, microstructure, and morphology were systematically investigated. With increasing MgCl2 concentration, more aragonite was obtained, reaching 94.9 % at 0.5 M MgCl2. Notably, at 0.1 M MgCl2, high length-to-diameter ratio aragonite whiskers with 16 were achieved. Introducing 1 wt% MS carbonated at optimal 0.1 M MgCl2 into cement increased the 3 d and 28 d compressive strengths by 17.8 % and 22 %, respectively. Moreover, an excellent CO2 sequestration capacity of up to 20.33 g CO2 per 100 g MS was obtained for the carbonated MS. Therefore, wet carbonated MS with high content aragonite whiskers is a promising method for MS high-value utilization while reducing cement usage and CO2 emission, as well as improving cement performance as underground filling material.

Bryophyte-Bioinspired Nanoporous AAO/C/MgO Composite for Enhanced CO2 Capture: The Role of MgO.

A composite material composed of anodized aluminum oxide (AAO), carbon (C), and magnesium oxide (MgO) was developed for CO2 capture applications. Inspired by the bryophyte organism, the AAO/C/MgO composite mirrors two primary features of these species-(1) morphological characteristics and (2) elemental composition-specifically carbon, oxygen, and magnesium. The synthesis process involved two sequential steps: electroanodization of aluminum foil followed by a hydrothermal method using a mixture of glucose and magnesium chloride (MgCl2). The concentration of MgCl2 was systematically varied as the sole experimental variable across five levels-1 mM, 2 mM, 3 mM, 4 mM, and 5 mM-to investigate the impact of MgO formation on the samples' chemical and physical properties, and consequently, their CO2 capture efficiency. Thus, scanning electron microscopy analysis revealed the AAO substrate's porous structure, with pore diameters measuring 250 ± 30 nm. The growth of MgO on the AAO substrate resulted in spherical structures, whose diameter expanded from 15 nm ± 3 nm to 1000 nm ± 250 nm with increasing MgCl2 concentration from the minor to major concentrations explored, respectively. X-ray photoelectron spectroscopy (XPS) analysis indicated that carbon serves as a linking agent between AAO and MgO within the composite. Notably, the composite synthesized with a 4 mM MgCl2 concentration exhibited the highest CO2 capture efficiency, as determined by UV-Vis absorbance studies using a sodium carbonate solution as the CO2 source. This efficiency was quantified with a 'k' constant of 0.10531, significantly higher than those of other studied samples. The superior performance of the 4 mM MgCl2 sample in CO2 capture is likely due to the optimal density of MgO structures formed on the sample's surface, enhancing its adsorptive capabilities as suggested by the XPS results.

Galvanic corrosion of carbon steel under concentration cell formation in MgCl2 solution as an inorganic pollutant and the effect of flow velocity

Abstract The wastewater of petroleum refineries consists of various corrosive pollutants that are harmful not only for human and living organisms but also for the equipment and materials exposed to it. The galvanic corrosion of carbon steel in MgCl2 solution as a pollutant in petroleum refinery wastewater was studied under concentration cell formation. The influence of different operating parameters on the galvanic corrosion established by concentration cell was studied, and the concept of concentration cell corrosion was examined and discussed versus experimental results. The effects of some operating conditions on the galvanic behavior, such as the concentration of MgCl2 (0–2500 ppm) and solution flow velocity (150–1000 rpm), on corrosion rate, corrosion potentials, and corrosion current were investigated. New findings regarding the effect of corrosive substance concentration and the hydrodynamics on the corrosion rate of each electrode and the galvanic current were reported. It was found that the corrosion rate of carbon steel in both cell poles increases with increasing MgCl2 concentration in both free and galvanic corrosion. Increasing MgCl2 concentration also led to an increase in the galvanic currents and the corrosion rate of the two electrodes. The flow velocity in either cell terminal considerably influences the potentials, corrosion rates of both electrodes, and the galvanic current passing in the cell. A high flow velocity in the compartment with the more negative potential caused polarity reversal on some occasions.

Solubility of U(VI) in chloride solutions. III. The stable oxides/hydroxides in MgCl2 systems: Pitzer activity model for the system UO22+–Na+–K+–Mg2+–H+–OH−–Cl−–H2O(l)

We have developed new chemical, thermodynamic and activity models for the system UO22+–Na+–K+–Mg2+–H+–OH−–Cl−–H2O(l) within the Pitzer approach. The new thermodynamic model is based on previously reported data treated within the SIT approach for NaCl and KCl systems, as well as on new experimental data determined in this work for the MgCl2 system.The solubility of uranium(VI) was studied in 0.01–5.15 mol·kgw−1 MgCl2 solutions at pHm = 4.1–9.7 (with pHm = −log [H+]). Experiments were performed under Ar atmosphere at T = (22 ± 2) °C. In all investigated systems, the solubility of U(VI) is controlled by metaschoepite, UO3·2H2O(cr). In contrast to previously investigated NaCl and KCl systems, no ternary Mg–U(VI)–OH(s) solid phases formed in alkaline MgCl2 solutions within the timeframe of this study (≤ 200 days). A very significant increase in the solubility (up to 3 log10-units) is observed in acidic to near-neutral pHm conditions when increasing MgCl2 concentration from 0.01 to 5.15 mol·kgw−1, which reflects the strong ion interaction processes taking place in concentrated MgCl2 brines.The solubility of UO3·2H2O(cr) in the investigated NaCl, KCl and MgCl2 solutions is well described with the solubility and hydrolysis constants recommended by Altmaier et al., (2017) and NEA–TDB, and a Pitzer activity model derived in the present work. The latter model considers experimental data reported in the present study and available in the literature for NaCl, KCl and MgCl2 systems (solubility, potentiometric and spectroscopic data), in combination with well-stablished estimation methods and correlations with SIT coefficients.Chemical, thermodynamic and Pitzer activity models provided in this work for the system UO22+–Na+–K+–Mg2+–H+–OH−–Cl−–H2O(l) accurately describe all evaluated datasets, and represent an adequate tool for the calculation of U(VI) solubility and aqueous speciation in a variety of geochemical conditions including concentrated brine systems of relevance in salt-based repositories for nuclear waste disposal.

Role of Chloride for a Simple, Non-Grignard Mg Electrolyte in Ether-Based Solvents.

Mg battery operates with Chevrel phase (Mo6S8, ∼1.1 V vs Mg) cathodes that apply Grignard-based or derived electrolytes, which allow etching of the passivating oxide coating forms at the magnesium metal anode. Majority of Mg electrolytes studied to date are focused on developing new synthetic strategies to achieve a better reversible Mg deposition. While most of these electrolytes contain chloride as a component, and there is a lack of literature which investigates the fundamental role of chloride in Mg electrolytes. Further, ease of preparation and potential safety benefits have made simple design of magnesium electrolytes an attractive alternative to traditional air sensitive Grignard reagents-based electrolytes. Work presented here describes simple, non-Grignard magnesium electrolytes composed of magnesium bis(trifluoromethane sulfonyl)imide mixed with magnesium chloride (Mg(TFSI)2-MgCl2) in tetrahydrofuran (THF) and diglyme (G2) that can reversibly plate and strip magnesium. Based on this discovery, the effect of chloride in the electrolyte complex was investigated. Electrochemical properties at different initial mixing ratios of Mg(TFSI)2 and MgCl2 showed an increase of both current density and columbic efficiency for reversible Mg deposition as the fraction content of MgCl2 increased. A decrease in overpotential was observed for rechargeable Mg batteries with electrolytes with increasing MgCl2 concentration, evidenced by the coin cell performance. In this work, the fundamental understanding of the operation mechanisms of rechargeable Mg batteries with the role of chloride content from electrolyte could potentially bring rational design of simple Mg electrolytes for practical Mg battery.

Effect of magnesium salt concentration in water-in-oil emulsions on the physical properties and microstructure of tofu

The aim of this research was to prepare water-in-oil (W/O) emulsions encapsulating different concentrations of magnesium chloride (MgCl2) and to investigate the effect of W/O emulsions on the physical properties and microstructure of tofu. The results showed that the stability of W/O emulsions improved as the concentrations of polyglycerol polyricinoleate (PGPR) and MgCl2 increased. Dynamic viscoelastic measurements indicated that gelation time decreased with increasing MgCl2 concentration in W/O emulsions, suggesting a more rapid reaction between magnesium ions and protein molecules. As the concentration of MgCl2 in W/O emulsions increased, the yield and water content of tofu decreased, while the protein and crude fat contents and hardness values increased. At a concentration of 2.0M MgCl2 in W/O emulsion, the WHC and microstructure of the tofu samples were optimal. The variations in the physical properties of tofu were attributed to the concentration of magnesium ions and the coagulation rate.

Effects of modification with glutaraldehyde on the mechanical properties of wood

Abstract Scots pine (Pinus sylvestris L.) sapwood was treated with glutaraldehyde (GA) and magnesium chloride (MgCl2) as a catalyst. The effects of treating conditions on the mechanical properties were examined. The weight percent gain (WPG) of thin veneer strips after leaching was highest at pH 4.0–4.5 and tensile strength measured in zero-span strength and finite-span strength decreased with decreasing pH in a range of 3.5–5.5. Sole treatment with MgCl2 also gradually decreased the tensile strength up to 25% with decreasing pH. At a fixed GA concentration (1.2 M), increasing MgCl2 concentration linearly diminished tensile strength. Conversely, increasing GA at a fixed MgCl2 concentration (1.5%) displayed the same effect, whereas in both cases zero-span strength loss was higher than finite span-strength loss. GA treatment of Scots pine sapwood stakes did not affect the modulus of rupture and the modulus of elasticity, but significantly reduced work to maximum load in bending and impact bending strength indicating embrittlement of wood. At the same time, compression strength increased with increasing WPG of GA. It is assumed that embrittlement caused by hydrolysis and crosslinking of cell wall polymers is compensated by enhanced compression strength thereby resulting in unchanged bending strength.

Temperature-Responsive Formation of Colloidal Nanoparticles from Poly(N-isopropylacrylamide) Grafted with Single-Stranded DNA

The thermal properties and temperature-responsive nanoparticle formation of poly(N-isopropylacrylamide) grafted with single-stranded DNA (PNIPAAm-g-DNA) were investigated. Copolymerization between nonamer single-stranded DNA with a vinyl group at its 5' terminus (DNA macromonomer) and NIPAAm was carried out so that the DNA macromonomer unit content should be less than 1 mol %. The turbidimetry and differential scanning calorimetry of the copolymer showed that the transition temperature increased and the enthalpy change of the phase transition decreased with increasing DNA macromonomer content in the copolymers, indicating that the DNA macromonomer behaves as a hydrophilic part in the copolymer and that the hydrophilicity is greater than that of sodium styrenesulfonate. Above the phase transition temperature, the copolymers formed colloidal nanoparticles with a dehydrated PNIPAAm core surrounded by DNA. When the formation of particles was conducted at higher temperatures, the dehydration of the copolymers proceeded such that the hydrodynamic radius (Rh) of the particles decreased. From the results of light scattering measurements, we calculated the surface area of particles occupied by one DNA (S(DNA)). The S(DNA) value decreased with increasing formation temperature, indicating that the DNA density on the particle surface increases with increasing formation temperature. The increase in the DNA density was also confirmed from the zeta-potential measurement of the particle. When MgCl2 was added to the copolymer solutions, the anionic charge of DNA was neutralized by Mg2+ so that Rh and the molecular weight of the particles increased with the increasing MgCl2 concentration. The turbidimetric detection of a target DNA was successfully demonstrated by utilizing the stability decrease of the colloidal particle upon hybridization on the particle surface.

Ionic Species Involved in the Electrical Activity of Single Adult Aminergic Neurones Isolated from the Sixth Abdominal Ganglion of the Cockroach Periplaneta Americana

ABSTRACT Adult neurones were obtained by dissociation of the dorsal area of the sixth abdominal (A6) ganglion of the cockroach, and electrical properties were studied with the patch-clamp technique. The neurones showed spontaneous fast action potentials, similar to those recorded with microelectrodes in neurones in situ along the dorsal median line of the A6 ganglion. Synthetic saxitoxin (sSTX) at concentrations of 10 × 10−8 to 1·0×10−7moll−1 suppressed the action potential (AP) and induced a dose-dependent hyperpolarization of the resting potential, suggesting that two types of sSTX-sensitive Na+ channels are present. The resting potential was dependent on the external concentration of both Na+ and K+, with a similar sensitivity to each, yielding a slope of about 43 mV per 10-fold change in concentration. The delayed outward rectification present under control conditions was reduced by tetraethylammonium chloride (TEA-CI, 1·0×10−2moll−1). TEA-CI or Ca2+-free saline abolished the afterhyperpolarization and increased the overshoot and duration of triggered APs, indicating that a calcium-activated potassium conductance contributes to the falling phase of the AP. At 3·0×10−3moll−1, the Ca2+ channel blockers MnCl2, CoCl2 and NiCl2 lengthened the AP. A blocker-dependent increase in the overshoot and threshold of the AP and reduction of the afterhyperpolarization were observed, probably reflecting the relative potencies of these ions in blocking Ca2+ channels and thus the Ca2+-activated K+ conductance. Increasing MgCl2 concentration by 3·0 ×10−3moll−1 had no effect on the AP, indicating that the positive shift of the threshold is due to the blockade of Ca2+ channels present at this potential. The results suggest that these isolated neurones are dorsal unpaired median neurones previously studied in a number of insect species.

Histochemical localization of skin glycosaminoglycans during feather development in the chick embryo.

The distribution of glycosaminoglycans (GAGs) was studied in embryonic chick skin, using alcian blue staining with critical electrolyte concentration and glycanase treatment, immunofluorescence and transmission electron microscopy. Light microscopy revealed an uneven distribution of sulphated and non-sulphated GAGs at all stages of feather development. Along the dermal-epidermal junction and throughout the depth of the dermis, staining was stronger inside the feathers than in the interplumar skin. With increasing MgCl2 concentration, the decrease in stain intensity along the dermal-epidermal junction was stronger in interplumar skin than inside feather structures, indicating that sulphated GAGs are more abundant within feathers than in interplumar skin. The same differential sensitivity to electrolyte concentration was noted in the dermis, except at the feather placode stage, when labelling inside the dermal condensation was virtually wiped out at 0.6 M MgCl2 and higher concentrations, whereas it persisted in the surrounding dermis up to 0.8 M MgCl2, indicating that the dermal condensation contains a larger amount of hyaluronate than non-feather-forming dermis. Enzyme treatment of sections with Streptomyces hyaluronidase as compared with those treated with chondroitinase ABC corroborated these findings. Immunofluorescent detection of heparan sulphate proteoglycan revealed the presence of the antigen along the dermal-epidermal junction at all stages of feather development, with peaks of brightness in discrete spots of feather structures. Electron microscopy revealed the presence of ruthenium red and tannic acid positive material in the dermal-epidermal junctional zone and inside the dermis. The density of marked granules was somewhat higher in intraplumar than in interplumar regions. These observations demonstrate that certain sulphated and non-sulphated GAGs are distributed in a microheterogeneous manner, which appears to be related to the morphogenetic events of feather development. They are discussed in view of the possible role these components might play in dermal-epidermal interactions. They strengthen the notion, already gained from previous studies on the localization of interstitial collagens and fibronectin, that extracellular matrix components play an important structural and informative role in organogenesis.

ＳＵＳ３０４鋼単結晶のＭｇＣｌ２溶液中における応力腐食割れとその電位依存性

The susceptibility to stress corrosion cracking (SCC) and its potential dependence were examined for SUS 304 steel single crystals with the single slip orientation, i.e., 0.50 in Schmid factor.The SCC tests were carried out in boiling 25-45% MgCl2 solutions under various constant potentials in the present study.The corrosion morphology of the specimen surface SCC-tested was dependent on both MgCl2 concentration and applied potential: The potential range for SCC occurrence of which critical potential was -380--400mV (SCE) increased with increasing MgCl2 concentration. In this case, the threshold concentration for cracking was about 30%, below which the potential range for pitting appeared. The uneven general corrosion occured as the potential was shifted to more noble values. On the other hand, the cracks mentioned above initiated from the specimen surface which was easy to induce slip-steps by plastic deformation. The fracture surface characterized by river-like pattern was formed by the crack growth along ‹110› direction on {110} plane.

Proton movements and electric potential generation in reconstituted ATPase proteoliposomes from the thermophilic cyanobacterium Synechococcus 6716.

ATP hydrolysis-induced proton translocation and electric potential generation have been studied in ATPase proteoliposomes by means of various optical probes. The proteoliposomes consisted of reconstituted ATPase complex and native lipid mixture isolated from the thermophilic cyanobacterium Synechococcus 6716 [Van Walraven et al. (1983) Eur. J. Biochem. 137, 101-106]. The native cartenoids and added oxonol VI served as probes for the electric membrane potential generated by the net charge separation (negative outside, positive inside). Their responses, with similar half-times as 9-tetradecylamino-6-chloro-2-methoxyacridine, are sensitive to valinomycin and stimulated by nigericin, as expected. The proton concentrations of extraliposomal and intraliposomal aqueous spaces were monitored by neutral red and cresol red; for internal measurements these pH indicators were trapped inside the vesicles during detergent dialysis. Internal acidification and external alkalinization induced by ATP hydrolysis are inhibited by nigericin and enhanced by valinomycin; at the commonly used higher valinomycin concentrations the neutral red response becomes transient, while the much slower cresol red response is diminished right from its onset. At smaller preset pH gradients both ATP hydrolysis activity and neutral red response are diminished. At increasing MgCl2 concentrations the neutral red responses are slowed down and the cresol red responses are slightly enhanced; this is observed for both internal and external dye responses. Neutral red permeation through the membrane is insignificant under our experimental conditions but is enhanced at temperatures below the lipid-phase transition. In the case of externally added neutral red the non-permeant buffer Hepes is only effective at high MgCl2 concentration, whereas some external cresol red response is visible only at high MgCl2 concentration in the presence of Hepes. The kinetics of the pH indicator and electric potential probe responses clearly distinguish fast interfacial and intra-membrane proton displacements from slow bulk proton equilibration. The data are summarized in a model that supports the importance of localized proton displacements for the primary energy-transducing events.

?-1-3- and ?-1-4-glucan synthesis by membrane fractions from the fungus Saprolegnia

The β-glucan synthetase activity of the fungus Saprolegnia monoica was assayed by supplying UDP-glucose to membrane fractions of mycelial homogenate. The analysis of glucan products by hydrolysis with various β-glucanases and by chromatography show that both β-1-3- and β-1-4-linkages are formed at high substrate concentrations. In the absence of MgCl2, β-1-3-linked glucans are mainly produced. By increasing MgCl2 concentrations the total synthesis activity and β-1-3-linkages production are reduced. At low substrate concentrations in the presence of MgCl2, β-1-4-linked glucans are the only polysaccharide synthesized. Electron microscopy of radioactive products, synthesized by original membrane fractions or by membrane fractions isolated from continuous sucrose density gradients, shows microfibrils when the assays are conducted at high substrate concentrations in the absence of MgCl2.

Modulation of the response of bovine adrenocortical adenylate cyclase to corticotropin

An assessment was made of some of the basic parameters responsible for the modulation of adenylate cyclase activity in a bovine adrenocortical plasma-membrane preparation. When determined at 0.1 mM-ATP, basal adenylate cyclase activity increased with increasing MgCl2 concentrations, whereas in the presence of corticotropin activity was essentially maximal at 10mM-MgCl2; high concentrations (25mM) of MgCl2 inhibited adenylate cyclase activity determined in the presence of both corticotropin and GTP. At all MgCl2 concentrations, corticotropin and GTP activated the enzyme in a synergistic fashion. The magnitude of the stimulation of basal activity produced by corticotropin was a function of Mg2+ concentration, whereas that produced by GTP appeared largely independent of Mg2+ concentration. Adenylate cyclase activity in the bovine adrenal membrane was half-maximally stimulated by corticotropin concentrations in the range 0.3--1.0 nM. The concentration of corticotropin evoking half-maximum response was not significantly affected by raising the free Mg2+ concentration from 0.4 to 4.9 mM, nor by the presence of GTP. In the presence of GTP, high concentrations (over 1 micrometer) of corticotropin inhibited adenylate cyclase activity, although no inhibition was apparent in the absence of guanine nucleotide.

Comparative Enzymatic Properties of Avian Liver and Skeletal Muscle D-Fructose-1,6-bisphosphate 1-Phosphohydrolase

The enzymatic properties of purified preparations of chicken liver and chicken skeletal muscle fructose bisphosphatases (D-fructose-1,6-bisphosphate 1-phosphohydrolase, EC 3.1.3.11) were compared. Both enzymes have an absolute requirement for Mg2+ or Mn2+. The apparent Km for MgCl2 at pH 7.5 was 0.5 mM for the muscle enzyme and 5 mM for the liver enzyme. Fructose bisphosphate inhibited both enzymes. At pH 7.5, the inhibitor constants (Ki) were 0.18 and 1.3 mM for muscle and liver fructose bisphosphatases, respectively. The muscle enzyme was considerably more sensitive to AMP inhibition than the liver enzyme. At pH 7.5 and in the presence of 1 mM MgCl2, 50% inhibition of muscle and liver fructose bisphosphatases occurred at AMP concentrations of 7 X 10(-9) and 1 X 10(-6) M, respectively. EDTA activated both enzymes. The degree of activation was time and concentration dependent. The degree of EDTA activation of both enzymes decreased with increasing MgCl2 concentration. Ca2+ was a potent inhibitor of both liver (Ki, 1 X 10(-4) M) and muscle (Ki, 1 X 10(-5) M) fructose bisphosphatase. This inhibition was reversed by the presence of EDTA. Ca2+ appears to be a competitive inhibitor with regard to Mg2+. There is, however, a positive homeotropic interaction among Mg2+ sites of both enzymes in the presence of Ca2+.

Thermal inactivation of avian liver and muscle fructose 1,6-diphosphatases in the presence of fructose 1,6-diphosphate, AMP, and divalent cations.

The effects at various pH levels of fructose 1,6-diphosphate (FDP), AMP, CaCl2, MnCl2, and/or MgCl2 on the thermal stability of pure forms of avian liver and muscle fructose 1,6-diphosphatases were investigated. Both enzymes were more stable when stored at 20 °C than at 2 °C. Maximum stabilities of the two enzymes when incubated at various temperatures in a Tris buffer occurred at approximately pH 6. All of the above compounds when added to a pH 7.5 Tris buffer markedly increased the thermal stabilities of both enzymes. Individually, FDP provided the highest degree of protection for the muscle enzyme whereas MnCl2 was most effective with the liver enzyme; in all cases the degree of protection was concentration dependent. At pH 7.5 combinations of MgCl2, FDP, and AMP were most effective. In the presence of these compounds initial inactivation of the muscle and liver enzymes did not occur until respective temperatures of 74 and 78 °C (15 min) were reached; these compare with initial inactivation temperatures in the absence of these compounds of 55 and 59 °C. The interaction of MgCl2 and FDP with the two enzymes at varying pH levels showed markedly different patterns. At pH7.5 and 8.8 increasing levels of MgCl2 provided increasing levels of protection whereas at pH 6.2 increasing MgCl2 concentrations resulted in an enhanced degree of inactivation. In the presence of FDP an opposite pattern was observed at the various pH levels. The presence of phosphate in the buffer tended to yield results similar to those of FDP.