Lime/Sodium Carbonate Treated Seawater to Improve Flocculation and Sedimentation of Clay-Based Tailings

Seawater treated with lime and sodium carbonate in different proportions to reduce magnesium and calcium contents is used in flocculation and sedimentation tests of artificial quartz and kaolin tailings. Solid complexes were separated from water by vacuum filtration, and factors such as lime/sodium carbonate ratio, kaolin content, flocculation time, and flocculant dose are evaluated. The growth of the aggregates was captured in situ by a focused beam reflectance measurement (FBRM) probe. Solid magnesium and calcium complexes are formed in raw seawater at pH 11, impairing the performance of flocculant polymers based on polyacrylamides. The results show that the settling rate improved when the treatment’s lime/sodium carbonate ratio increased. That is, when a greater removal of magnesium is prioritized over calcium. The amount of magnesium required to be removed depends on the mineralogy of the system: more clay will require more significant removal of magnesium. These results respond to the structural changes of the flocs, achieving that the more magnesium is removed, the greater the size and density of the aggregates. In contrast, calcium removal does not significantly influence flocculant performance. The study suggests the necessary conditions for each type of tailing to maximize water recovery, contributing to the effective closure of the water cycle in processes that use seawater with magnesium control.

Molecular Properties of Bare and Microhydrated Vitamin B5–Calcium Complexes

Pantothenic acid, also called vitamin B5, is an essential nutrient involved in several metabolic pathways. It shows a characteristic preference for interacting with Ca(II) ions, which are abundant in the extracellular media and act as secondary mediators in the activation of numerous biological functions. The bare deprotonated form of pantothenic acid, [panto-H]−, its complex with Ca(II) ion, [Ca(panto-H)]+, and singly charged micro-hydrated calcium pantothenate [Ca(panto-H)(H2O)]+ adduct have been obtained in the gas phase by electrospray ionization and assayed by mass spectrometry and IR multiple photon dissociation spectroscopy in the fingerprint spectral range. Quantum chemical calculations at the B3LYP(-D3) and MP2 levels of theory were performed to simulate geometries, thermochemical data, and linear absorption spectra of low-lying isomers, allowing us to assign the experimental absorptions to particular structural motifs. Pantothenate was found to exist in the gas phase as a single isomeric form showing deprotonation on the carboxylic moiety. On the contrary, free and monohydrated calcium complexes of deprotonated pantothenic acid both present at least two isomers participating in the gas-phase population, sharing the deprotonation of pantothenate on the carboxylic group and either a fourfold or fivefold coordination with calcium, thus justifying the strong affinity of pantothenate for the metal.

Changes in the secondary structures and zeta potential of soybean peptide and its calcium complexes in cell membrane medium

In this study, soybean peptides (10-30kDa) with high calcium binding capacity were prepared by enzymatic hydrolysis and ultrafiltration. The results of cell experiments showed that the peptide could transport calcium...

C–H and C–F coordination of arenes in neutral alkaline earth metal complexes

A series of neutral magnesium and calcium complexes bearing an extremely bulky diamido ligand have been synthesised and crystallographically characterised. A number of these complexes feaure rare group 2 metal···aromatic...

Stereoselective polymerization of rac-lactide catalyzed by zwitterionic calcium complexes

Two zwitterionic calcium complexes L1CaN(SiMe3)2(THF) (1) and L2CaN(SiMe3)2 (2) via protolysis reaction were synthesized. At −75 °C, 1 gave a heterotactic sequence enriched polylactide, whilst 2 produced an isotactic sequence enriched polymer.

Polyelectrolyte–calcium complexes as a pre-precursor induce biomimetic mineralization of collagen

Rapid biomimetic intrafibrillar mineralization of collagen was induced by polyelectrolyte–calcium complexes as a pre-precursor.

Investigations of mechanism of Ca2+ adsorption on silica and alumina based on Ca-ISE monitoring, potentiometric titration, electrokinetic measurements and surface complexation modeling

Research on Ca2+ adsorption onto the mineral surface is of significant importance with regard to geochemical processes. Sverjensky (Geochim Cosmochim Acta 70(10), 2427–2453, 2006) assumed that alkaline earths form two types of surface species on oxides: tetranuclear (> SOH)2(> SO−)2_M(OH)+ and mononuclear > SO−_M(OH)+. To look into the above assumption we investigated calcium adsorption on SiO2 and Al2O3 because they are the most widespread minerals in the environment. We have determined the proton surface charge, electrokinetic potential and metal adsorption as a function of pH. The Ca2+ uptake and concentration in the system were monitored by the calcium ion-selective electrode (Ca-ISE). The Ca-ISE measurements indicated a similar affinity of Ca2+ for both materials despite their differently charged surface, negative for silica and mainly positive for alumina. This may suggest that simple electrostatic interactions are not the primary driving force for calcium adsorption, and that solvation of calcium ions at the surface may be crucial. We have analyzed our experimental data using the 2-pK triple-layer model (2-pK TLM). Three calcium complexes on the mineral surface were reported. Two of them were the same for both oxides, i.e. the tetranuclear ($$>$$ > SOH)2($$>$$ > SO−)2_Ca2+ and mononuclear complexes > SO−_CaOH+. Additionally, minor contribution from >SOH…Ca2+ for silica was assumed. In the case of Al2O3 the hydrolyzed tetranuclear complexes ($$>$$ > SOH)2($$>$$ > SO−)2_CaOH+ at pH > 7.5 occurred based on the modeling results. Two types of surface complexes suggested by Sverjensky allowed for the correct description of proton and calcium uptake for alumina. However, the electrokinetic data excluded hydrolyzed tetranuclear surface species for this oxide.