Addition Of Calcium Research Articles

Online Supervisory System for In-Process Optimization of Calcium Additions by Continuously Monitoring the State of Non-metallic Inclusions Inside Low-Alloyed Liquid Steels

A decision support system was developed using supervised machine learning (ML) approach for optimization of calcium (Ca) additions by continuously monitoring the physical state of non-metallic inclusions (NMIs) inside low-alloyed liquid steels. In this work, two instances were considered to design the base algorithm for the proposed supervisory system: (1) Clogging of submerged entry nozzle (SEN) during continuous casting of steels due to accumulation of solid oxide non-metallic inclusions (NMIs) and (2) Ca treatment during secondary steelmaking for modification of oxide NMIs from solid to liquid state to avoid SEN clogging. At first, experimental investigations were carried out on liquid steel samples from three low-alloyed Ca-treated steel grades from the same steel family to evaluate the characteristics of solid oxide NMIs that cause SEN clogging. In the next step, data-driven models were developed using an in-house ML algorithm trained primarily with process data for calculating the value of the newly proposed dummy parameter ‘Clog.’ These models, after testing, were architected to develop a supervisory system based on experimental investigations and data-driven models. The objective of this proposed supervisory system was to predict the optimum quantity of Ca needed for successful modification of NMIs from solid to liquid state to avoid SEN clogging based on the forecasted ‘Clog’ value. Finally, industrial data from ~ 3000 heats were tested to verify the results obtained from the developed supervisory system. The results confirmed that this novel supervisory system could predict the optimum class of Ca for all studied steel grades with 95 to 98 pct accuracy. The integration of this online supervisory system in steel production is expected to minimize operators’ corrective actions in achieving realistic control of Ca additions.

Hypothermia Inhibits Dexmedetomidine-Induced Contractions in Isolated Rat Aortae.

Dexmedetomidine is widely used to induce sedation in the perioperative period. This study examined the effect of hypothermia (33 and 25 °C) on dexmedetomidine-induced contraction in an endothelium-intact aorta with or without the nitric oxide synthase inhibitor NW-nitro-L-arginine methyl ester (L-NAME). In addition, the effect of hypothermia on the contraction induced by dexmedetomidine in an endothelium-denuded aorta with or without a calcium-free Krebs solution was examined. The effects of hypothermia on the protein kinase C (PKC), myosin light chain (MLC20) phosphorylation, and Rho-kinase membrane translocation induced by dexmedetomidine were examined. Hypothermia inhibited dexmedetomidine-induced contraction in the endothelium-intact aorta with L-NAME or endothelium-denuded aorta. Hypothermia had almost no effect on the dexmedetomidine-induced contraction in the endothelium-denuded aorta with the calcium-free Krebs solution; however, the subsequent contraction induced by the addition of calcium was inhibited by hypothermia. Conversely, the transition from profound hypothermia back to normothermia reversed the hypothermia-induced inhibition of subsequent calcium-induced contractions. Hypothermia inhibited any contraction induced by KCl, PDBu, and NaF, as well as PKC and MLC20 phosphorylation and Rho-kinase membrane translocation induced by dexmedetomidine. These results suggest that hypothermia inhibits dexmedetomidine-induced contraction, which is mediated mainly by the impediment of calcium influx and partially by the attenuation of pathways involving PKC and Rho-kinase activation.

The effect of calcium addition on the nitrogen removal performance of an activated sludge system from a microbiological perspective

The effect of calcium addition on the nitrogen removal performance of an activated sludge system from a microbiological perspective

Addition of substances to reduce the erosive potential of acidic beverages to tooth enamel: A scoping review.

This scoping review aimed (1) to map, analyse, interpret and synthesize data from insitu studies on which substances were added to acidic beverages to reduce the erosive potential on tooth enamel and (2) to establish the level of evidence of the effectiveness of adding substances to acidic beverages to reduce the erosive potential on tooth enamel. This is a scoping review, according to the methods from the Joanna Briggs Institute and PRISMA-ScR, with high-sensitivity searches in the databases PubMed (MEDLINE), Virtual Health Library, Embase (Elsevier), Scopus (Elsevier), Web of Science and ScienceDirect (Elsevier). Insitu studies published in English until December 2022 were included. Studies that did not report a control group were excluded. To map and summarize the results, tables and figures were used. From 895 potentially eligible articles, nine were included. Blackcurrant juices (n = 5) with the addition of calcium (n = 3) or xanthan gum (n = 2) formulations were the most tested in terms of reducing the erosive potential of the beverages on tooth enamel. The profilometer was the equipment of choice (n = 8) for evaluating the loss of enamel structure after the experimental tests. Calcium and xanthan gum are among the most tested by insitu studies, offering promising results in reducing the erosive potential of fruit juices and carbonated and energy drinks.

High-temperature transport properties of entropy-stabilized pyrochlores

In this report, the high-temperature transport properties of (Dy1−xCax)(Zr0.2Hf0.2Sn0.2Ti0.2Ge0.2)O7 pyrochlore oxides with x = 0, 0.05, and 0.1 are studied in dry and humid air. The phase composition and crystal structure were determined by using x-ray and neutron diffraction. The addition of calcium to the structure caused an increase in the concentration of oxygen vacancies, indicating an ionic charge compensation mechanism. Electrical studies allowed us to determine the total electrical conductivity as a function of the synthesis atmosphere and pH2O. The electrical conductivity turned out to be at the level of ∼10−3 S/cm at 800 °C, and only a slight effect of the presence of protonic defects in the structure on the total electrical conductivity was observed. In general, the samples had a low electrical conductivity with a relatively high activation energy of conduction.

Influence of alkaline earth metals on the corrosion-electrochemical behavior of lead babbit BKa, BSt, BBa (PbSb15Sn10) in NaCl electrolyte medium

The article presents the results of study of the effect of additions of calcium, strontium and barium (0.01–1.0 wt %) as a structure modifier on the anodic behavior of lead babbits BKa, BSt, BBa (PbSb15Sn10) in NaCl electrolyte medium. The studies were carried out by the potentiostatic method in a potentiodynamic mode with a potential sweep rate of 2 mV/s.Studies show that with time the free corrosion potential of alloys shifts to the positive side, and with an increase in the concentration of the modifier (calcium, strontium and barium) in lead babbits, acquires a positive value. The addition of calcium to lead babbit BKa (PbSb15Sn10Ca) increases its corrosion resistance by 10 – 15%, strontium BST (PbSb15Sn10Sr) by 15–20%, and barium BBa (PbSb15Sn10Ba) by 20–25%. An increase in the corrosion rate of alloys was noted, regardless of t heir composition from the NaCl concentration in the solution. It has been shown that an increase in the chloride ion concentration in the NaCl electrolyte leads to a decrease in the potentials of free corrosion, repassivation, and pitting formation of alloys.

Effect of Individual Alloying Addition on the Microstructure and Creep Behavior of Squeeze Cast AZ91 Magnesium Alloy

The microstructure of AZ91 (Mg-Al) alloy is comprised of α-Mg and β-Mg17Al12 massive phase. The lower melting point associated with the β-Mg17Al12 phase results in poor creep resistance of the alloy. In the present study, the AZ91 alloy with the addition of calcium (Ca, 1wt%) and cerium (Ce, 1wt%) is cast, and their effect on the microstructure and creep behavior of AZ91 alloy have been investigated. Thermally stable phases such as Al2Ca and Al11Ce3 are introduced in the AZ91 alloy through the addition of Ca and Ce elements. Energy dispersive spectroscopy (EDS) and x-ray diffraction analysis confirmed the presence of these intermetallic phases in the microstructure. Tensile creep tests on the as-cast samples were performed at 175°C temperature under 50 MPa stress. The study shows that the creep resistance of AZ91 alloy is greatly improved with the presence of Al2Ca and Al11Ce3 intermetallic phases because of their better thermal stability than β-Mg17Al12.

Band gap engineering through calcium addition in (Mg, Co, Ni, Cu, Zn)O high entropy oxide for efficient photocatalysis

Multicomponent metal oxides have shown the potential to be excellent catalysts mainly because of synergistic interactions between the active sites. We report (Co, Mg, Ni, Cu, Zn)1-xCaxO (x = 0.05, 0.1) high entropy oxide (HEO) photocatalyst with single phase rocksalt structure (space group Fm3¯m) synthesized by solution combustion synthesis (SCS) technique. HEOs contain elements with varying electronegativities and crystal field splitting and thus exhibit a relatively lower band gap when compared to the individual constituent oxides. Adding Ca2+ results in increased covalency due to the greater exchange interaction between O 2p and transition metal (TM) 3d orbital, engendering further reduction in band gap and consequently improving photocatalytic activity in the visible region. In addition, the introduction of point defects, mainly metal/oxygen vacancy, to accommodate the larger size Ca2+ cation also contributed to the catalytic activity. The photocatalytic activity enhancement is demonstrated by visible light-assisted photodegradation of methylene blue (MB). The MB dye degradation rate constant for (Co, Ni, Cu, Zn, Mg)0.9Ca0.1O catalyst was found to be ∼0.0445 min−1, which was about six times faster than that of the pristine (Co, Mg, Ni, Cu, Zn)O.

Effect of calcium and potassium oxide addition on the viscosity and fragility of a calcium aluminosilicate melt

AbstractFragility is commonly quantified as the magnitude of change in viscosity at a temperature close to the glass transition temperature (Tg). It is a critical characteristic of melts used in scientific and industrial applications. The fragility of silicate melts generally increases with the depolymerization of silicate anions upon the addition of alkali or alkaline earth oxides. However, the effects of oxide additives on the fragility of aluminosilicate melts remain unclear. In this study, the effect of CaO or K2O addition on the viscosity of the 36CaO–51SiO2–13Al2O3 (mol.%) melt for the wide viscosity range of 10−1–1012 Pa s was studied. The relationship between the logarithmic viscosity and Tg‐scaled temperature indicated that the melt fragility increased with the addition of CaO, whereas the addition of K2O reduced the fragility when the additive content of CaO or K2O was less than 10.8 mol.%. The effect of the addition of K2O on fragility cannot be explained by the depolymerization of silicate anions alone. Raman and 27Al nuclear magnetic resonance spectroscopies of the glasses indicated that a decrease in the level of distortion of the AlO4 tetrahedra decreased the fragility of the aluminosilicate melt.

Klebsiella pneumoniae DedA family proteins have redundant roles in divalent cation homeostasis and resistance to phagocytosis.

The DedA superfamily is a highly conserved family of membrane proteins. Deletion of Escherichia coli yqjA and yghB, encoding related DedA family proteins, results in sensitivity to elevated temperature, antibiotics, and alkaline pH. The human pathogen Klebsiella pneumoniae possesses genes encoding DedA family proteins with >90% amino acid identity to E. coli YqjA and YghB. We hypothesized that the deletion of K. pneumoniae yqjA and yghB will impact its physiology and may reduce its virulence. The K. pneumoniae ΔyqjA ΔyghB mutant (strain VT101) displayed a growth defect at 42°C and alkaline pH sensitivity, not unlike its E. coli counterpart. However, VT101 retained mostly wild-type resistance to antibiotics. We found VT101 was sensitive to the chelating agent EDTA, the anionic detergent SDS, and agents capable of alkalizing the bacterial cytoplasm such as bicarbonate or chloroquine. We could restore growth at alkaline pH and at elevated temperature by addition of 0.5-2 mM Ca2+ or Mg2+ to the culture media. VT101 displayed a slower uptake of calcium, which was dependent upon calcium channel activity. VT201, with similar deletions as VT101 but derived from a virulent K. pneumoniae strain, was highly susceptible to phagocytosis by alveolar macrophages and displayed a defect in the production of capsule. These findings suggest divalent cation homeostasis and virulence are interlinked by common functions of the DedA family.IMPORTANCEKlebsiella pneumoniae is a dangerous human pathogen. The DedA protein family is found in all bacteria and is a membrane transporter often required for virulence and antibiotic resistance. K. pneumoniae possesses homologs of E. coli YqjA and YghB, with 60% amino acid identity and redundant functions, which we have previously shown to be required for tolerance to biocides and alkaline pH. A K. pneumoniae strain lacking yqjA and yghB was found to be sensitive to alkaline pH, elevated temperature, and EDTA/SDS and displayed a defect in calcium uptake. Sensitivity to these conditions was reversed by addition of calcium or magnesium to the growth medium. Introduction of ΔyqjA and ΔyghB mutations into virulent K. pneumoniae resulted in the loss of capsule, increased phagocytosis by macrophages, and a partial loss of virulence. These results show that targeting the Klebsiella DedA family results in impaired divalent cation transport and, in turn, loss of virulence.

The role of calcium in the prevention of erosive tooth wear: a systematic review and meta-analysis.

The loss of hard dental tissue due to recurrent acid challenges and mechanical stresses without bacterial involvement is known as erosive tooth wear (ETW). Many studies in the literature have concentrated on variables that may affect the ETW process and prevent its occurrence or reduce its advancement. However, to date, no previous systematic review has evaluated the role of calcium in preventing ETW. Therefore, the purpose of the present systematic review was to review and critically appraise the scientific evidence regarding the role of calcium formulations in the prevention of ETW. The review protocol was registered in the PROSPERO international prospective register of systematic reviews (Ref: CRD42021229819). A literature search was conducted in electronic databases to identify in situ randomized controlled trials evaluating the prevention of ETW following the application of calcium formulations. The outcomes studied included mean enamel loss, surface microhardness, surface roughness, mean erosion/softening depth, mineral loss/precipitation and remineralization. Study characteristics and outcomes of included studies were summarized. Cochrane's risk-of-bias tool 2.0 was used to assess the quality of eligible studies, and meta-analysis using a random effects model was performed. The search retrieved 869 studies of which 21 were considered eligible. Regarding the results of the quality assessment for potential risk of bias in all included studies, overall, 5 studies were considered as being at low risk, another 12 at unclear risk and 4 at high risk of bias. The findings of the studies showed that the addition of calcium in juice drinks led to reduced enamel loss, with blackcurrant juice presenting 2.6 times statistically significant less enamel loss compared to orange juice (p = 0.0001, I2 = 89%). No statistically significant difference in mean surface microhardness of eroded enamel was recorded between chewing gum with or without casein phosphopeptide-amorphous calcium phosphate (CPP-ACP) (p = 0.31, I2 = 71%). Contradictory were the results regarding the effect of milk and CPP-ACP pastes on prevention of ETW. Calcium formulations play an important role in ETW prevention, mainly through their addition to acidic drinks.

Effects of Calcium Addition on Nonmetallic Inclusions in High‐Al Steel

To investigate the formation and evolution mechanism of inclusions in high‐Al steel, four lab‐scaled experiments are carried out with different calcium (Ca) contents. The Al2O3 inclusions are modified to (CaO–Al2O3)–CaS after Ca addition. With the Ca content increased, the types of CAx‐CaS inclusions are changed from CaS‐attached inclusions to CAx‐wrapped inclusions. When the total calcium content (T.Ca) reached 29 ppm, the CAx–CaS inclusions are primarily distributed within the 50% liquidus in CaO–Al2O3–CaS ternary diagram. Some Al2O3 inclusions are not completely modified with 7 ppm Ca addition. CaS and CaO–CaS inclusions are observed with a higher Ca addition. The modification of Al2O3 by CaS and [Ca] occurs in CaS‐attached inclusions with a lower Ca addition. To clarify the formation of CaS, a new modification index for high‐Al steel is given based on the T.Ca/T.O index.

The influence of calcium addition on thermophysical properties and thermodynamic functions of aluminum alloy AlCu4.5Mg1

The influence of calcium addition on thermophysical properties and thermodynamic functions of aluminum alloy AlCu4.5Mg1

The effect of Ficoll 70 on thermally-induced and chemically-induced conformational transitions of an RTX protein is quantitatively accounted for by a unified excluded volume model.

A unified excluded volume model based upon the effective hard particle approximation is developed and used to quantitatively model previously published experimental measurements of the effect of adding high concentrations of an "inert" polymer, Ficoll 70, on conformational transitions of the toxin protein RCL that are induced by addition of calcium at constant temperature or by increasing temperature in the absence and presence of high calcium concentrations. The best-fit of this model, which accounts quantitatively for all of the published data to within experimental precision, yields an estimate of the volume of solution excluded to Ficoll by each of four identified conformational states of RCL: H - the most compact conformation adopted in the limits of high calcium concentration and low temperature, H* - the conformation adopted in the limits of high calcium concentration and high temperature, A - the conformation adopted in the limits of low (or no) calcium at low temperature, and A* - the conformation adopted in the limits of low calcium and high temperature. Ficoll exclusion volumes increase in the order H < H* < A < A*. These results are discussed in the context of the physiological functions of the RTX proteins, which are involved in the secretion process and the calcium-induced folding of bacterial virulence factors.

Metal ion cofactors modulate integral enzyme activity by varying differential membrane curvature stress.

Metal ions are well-known cofactors of protein function and stability. In the case of the integral membrane enzyme OmpLA (outer membrane phospholipase A) the active dimer is stabilized by calcium ions. We studied the lipid hydrolysis kinetics of OmpLA in charge-neutral and charged membranes with symmetric or asymmetric transbilayer lipid distributions. In charge-neutral membranes, OmpLA was more active in symmetric bilayers due to the lower differential curvature stress between membrane leaflets. Strikingly, this behavior was completely reversed in charged bilayers. Measurements revealed intrinsic molecular shape changes in the charged lipids upon addition of calcium. This effectively reduces the differential curvature stress in charged asymmetric membranes leading to increased protein activity. This conclusion is further supported by similar effects observed upon the addition of sodium ions, which also alter the shape of the lipids, but do not specifically interact with the protein. Additional lipid-protein interactions likely contribute to this phenomenon. Our findings demonstrate that ion cofactors not only interact directly with membrane proteins but also modulate protein activity indirectly by altering the effective molecular shape of charged lipid species.

Leveraging calcium-NOM complexation phenomenon as RO fouling mitigation strategy during treatment of lake water

Organic fouling during reverse osmosis (RO) is exacerbated by the presence of calcium up to a limit where extremely high calcium concentration results in lesser fouling due to formation of large organic-calcium aggregates with lower cake resistance. Therefore, this work leveraged on this phenomenon and used calcium chloride as coagulant (at varying concentration) to reduce membrane fouling while enhancing NOM removal. Membrane cleaning efficiency through calcium-EDTA chelation which disintegrates the fouling layers was explored. RO fouling was performed with sodium alginate solutions and lake water. The fouled membranes were soaked in 0.1 ​mM EDTA (1 ​h) and backwashed with water to remove the fouling layer. Alginate fouling was worsened (45–85 ​%) by increase in calcium concentration up to 5 ​mM but lessened at > 5 ​mM calcium concentration (35–15 ​%). Similar observations were made when filtering lake water, except that lesser fouling was observed at calcium concentrations greater than 15 ​mM. Membrane soaking in EDTA enhanced cleaning efficiency leading to over 90 ​% flux recovery for both alginate and late water. However, prolonged membrane exposure to 10 ​mM calcium resulted in slight decline in membrane salt rejection (<2 ​% change) and tensile stress (1.3–1.1 ​N/mm2), while the membrane flux increased (<3 ​% change). Finally, NOM removal improved with calcium addition (up to 90 ​%) – key in reducing potential formation of disinfection by-products due to addition of disinfection agents. The proposed use of calcium as a common coagulant/chelating agent for fouling mitigation/remediation during advanced membrane filtration has a potential for wider application and commercialization.

Expression, Purification, and Determination of Sensitivity to Calcium Ions of Ctenophore Photoproteins.

Light-sensitive Ca2+-regulated photoproteins of ctenophores are single-chain polypeptide proteins of 206-208 amino acids in length comprising three canonical EF-hand Ca2+-binding sites, each of 12 contiguous residues. These photoproteins are a stable complex of apoprotein and 2-hydroperoxy adduct of coelenterazine. Addition of calcium ions to photoprotein is only required to trigger bright bioluminescence. However, in contrast to the related Ca2+-regulated photoproteins of jellyfish their capacity to bioluminescence disappears on exposure to light over the entire absorption spectral range of ctenophore photoproteins. Here, we describe protocols for expression of gene encoding ctenophore photoprotein in Escherichia coli cells, obtaining of the recombinant apoprotein of high purity and its conversion into active photoprotein with synthetic coelenterazine as well as determination of its sensitivity to calcium ions using light-sensitive Ca2+-regulated photoprotein berovin from ctenophore Beroe abyssicola as an illustrative case.

Alkaline-earth ion stabilized sub-nano-platinum tin clusters for propane dehydrogenation.

The strong promotion effects of alkali/alkaline earth metals are frequently reported for heterogeneous catalytic processes such as propane dehydrogenation (PDH), but their functioning principles remain elusive. This paper describes the effect of the addition of calcium (Ca) on reducing the deactivation rate of platinum-tin (Pt-Sn) catalyzed PDH from 0.04 h-1 to 0.0098 h-1 at 873 K under a WHSV of 16.5 h-1 of propane. The Pt-Sn-Ca catalyst shows a high propylene selectivity of >96% with a propylene production rate of 41 molC3H6 (gPt h)-1 and ∼1% activity loss after regeneration. The combination of characterization and DFT simulations reveals that Ca acts as a structural promoter favoring the transition of Snn+ in the parent catalyst to Sn0 during reduction, and the latter is an electron donor that increases the electron density of Pt. This greatly suppresses coke formation from deep dehydrogenation. Moreover, it was found that Ca promotes the formation of a highly reactive and sintering-resistant sub-nano Pt-Sn alloy with a diameter of approximately 0.8 nm. These lead to high activity and selectivity for the Pt-Sn-Ca catalyst for PDH.

Effect of calcium addition on temperature dependence of thermophysical properties and changes in thermodynamic functions of lead babbit B (PbSb15Sn10)

Effect of calcium addition on temperature dependence of thermophysical properties and changes in thermodynamic functions of lead babbit B (PbSb15Sn10)

Thermoresponsive Alginate-Graft-pNIPAM/Methyl Cellulose 3D-Printed Scaffolds Promote Osteogenesis In Vitro.

In this work, a sodium alginate-based copolymer grafted by thermoresponsive poly(N-isopropylacrylamide) (PNIPAM) chains was used as gelator (Alg-g-PNIPAM) in combination with methylcellulose (MC). It was found that the mechanical properties of the resulting gel could be enhanced by the addition of MC and calcium ions (Ca2+). The proposed network is formed via a dual crosslinking mechanism including ionic interactions among Ca2+ and carboxyl groups and secondary hydrophobic associations of PNIPAM chains. MC was found to further reinforce the dynamic moduli of the resulting gels (i.e., a storage modulus of ca. 1500 Pa at physiological body and post-printing temperature), rendering them suitable for 3D printing in biomedical applications. The polymer networks were stable and retained their printed fidelity with minimum erosion as low as 6% for up to seven days. Furthermore, adhered pre-osteoblastic cells on Alg-g-PNIPAM/MC printed scaffolds presented 80% viability compared to tissue culture polystyrene control, and more importantly, they promoted the osteogenic potential, as indicated by the increased alkaline phosphatase activity, calcium, and collagen production relative to the Alg-g-PNIPAM control scaffolds. Specifically, ALP activity and collagen secreted by cells were significantly enhanced in Alg-g-PNIPAM/MC scaffolds compared to the Alg-g-PNIPAM counterparts, demonstrating their potential in bone tissue engineering.