Insights into the changes in the surface properties of goethite with Ni in the lattice in the presence of salicylhydroxamic acid:Experimental and density functional theory studies

Comparative experiments and theoretical analysis of the surface chemistry changes of goethite(GT)and goethite containing Ni(GTN)in the lattice in the presence of salicylhydroxamic acid(SA)were performed.It was revealed that in the presence of 100 g·t^(-1)of SA,the flotation recovery of GTN and GT increased with increasing pH,achieving a maximum recovery of 98.9%for both minerals at p H 8.3 and decreasing beyond that pH,with GTN having a slightly higher recovery than GT,except at pH 8.3.This was further confirmed by the higher complexation energies of GTN···SA(-883.87 kJ·mol^(-1))compared with GT···SA(-604.23 kJ·mol^(-1))resulting from covalent,closed-shell,and conventional hydrogen bonding.The higher adsorption of SA onto GTN relative to GT was due to the formation of aπ-hole in GTN,thereby promoting a higher interaction of the collector with the mineral.Thus,the presence of Ni in the GT lattice improves and decreases the adsorption and desorption of SA onto and from the mineral,respectively,compared with those onto and from GT.

Adsorption mechanism of mixed salicylhydroxamic acid and tributyl phosphate collectors in fine cassiterite electro-flotation system

Two reagents including salicylhydroxamic acid(SHA) and tributyl phosphate(TBP) were tested as collectors either separately or together for electro-flotation of fine cassiterite(<10 μm).Subsequently,the flotation mechanism of the fine cassiterite was investigated by adsorbance determination,electrophoretic mobility measurements and Fourier transform infra-red(FT-IR) spectrum checking.Results of the flotation experiments show that with SHA as a collector,the collecting performance is remarkably impacted by the pulp pH value as the floatability of cassiterite varies sharply when the pH changes,and flotation with SHA gives distinct maximum at about pH 6.5.Additionally,the floatability of cassiterite is determined by using SHA and TBP as collectors.The range of pulp pH for good floatability is broadened in the presence of TBP as auxiliary collector,and the utilization of TBP improves the recovery of cassiterite modestly.Moreover,the optimum pH value for cassiterite flotation is associated with adsorbance.The results of FT-IR spectrum and the electrophoretic mobility measurements indicate that the adsorption interaction between the collectors and the cassiterite is dominantly a kind of chemical bonding in the form of one or two cycle chelate rings due to the coordination of carbonyl group,hydroxamate and P=O group to the metal tin atoms,where the oxygen atoms contained in carbonyl group,hydroxamate and P=O group of the polar groups have the stereo conditions to form five-membered rings.In addition,the adsorption interactions of SHA and TBP on the surfaces of cassiterite are also dominated by means of hydrogen bonds.

Flotation behavior and adsorption mechanism of salicylhydroxamic acid in artificial mineral anosovite

Flotation is often employed to separate valuable natural minerals and gangue minerals.However,few studies have been conducted on artificial mineral flotation.Anosovite,the primary mineral in titanium slag,is a typical artificial mineral that can be enriched by flotation.In the present work,flotation behavior and adsorption mechanism of anosovite in salicylhydroxamic acid(SHA)solution were studied.The influence of pH and SHA dosage on anosovite flotability was investigated.Micro-flotation test results show that a pH range of 7–8.5 is available for SHA to collect anosovite.A maximum recovery of 93.26%can be obtained with SHA dosage of only 4×10.5 mol/L.In addition,TOC,zeta potential,FTIR,SEM-EDS,and XPS analyses were used to study the adsorption mechanism.Results demonstrated that SHA adsorption is governed by chemisorption.XPS studies further suggested that chemical adsorption occurred at the Ti sites on the anosovite surface.

Chelating Properties of Salicylhydroxamic Acid-functionalized Polystyrene Resins and Its Application to Efficient Removal of Heavy Metal Ions from Aqueous Solutions

Salicylhydroxamic acid（SHA） was covalently bound onto crosslinked polystyrene spheres（CPSs） via the Friedel-Crafts alkylation reaction between chloromethylated CPSs and SHA in the presence of SnCI4 as the Lewis acid catalyst. The resulted SHA-CPSs possessed very strong chelating ability for heavy metal ions. In particular, the saturated adsorption amount of SHA-CPSs for Cu2＋ ions could reach as high as 34.2 mg/g at 318 K. The chelating capability of SHA-CPSs towards heavy metal ions was pH and temperature dependent. SHA-CPSs also showed se- lective metal coordination with the chelating capacity decreasing in the order of Cu2＋ 〉Zn2＋〉〉Pb2＋. The adsorption isotherms conformed well to the Langmuir model, and the adsorption process was found to be entropy-driven and endothermic. Besides, SHA-CPSs possessed the excellent reusability.

Activity of Azoxystrobin and SHAM to Four Phytopathogens

The study was conducted to make clear the activity of azoxystrobin to 4 plant pathogens and the synergistic effects of salicylhydroxamic acid （SHAM）, which acted on the alternative oxidase. It was also conducted to be aware of the mechanism of azoxystrobin in inhibition on mycelial respiration and the influence of SHAM. The activity test of azoxystrobin and SHAM was carried out with a mycelial linear growth test and spore germination test. Other related biological properties were also observed. Inhibition of azoxystrobin and SHAM on 4 pathogens was determined by using SP-II oxygraph system. Azoxystrobin inhibited mycelial growth in Colletotrichum capsici, Botrytis cinerea, Rhizoctonia solani, and Magnaporthe grisea, respectively; it also inhibited conidia germination, and conidia production in C. capsici, B. cinerea M. grisea, and sclerotia formation in R. solani. Moreover, it created stayed pigment biosynthesis in C. capsici and M. grisea somehow. Salicylhydroxamic acid enhanced inhibition by azoxystrobin. An oxygen consuming test of the mycelia showed that azoxystrobin inhibited all the 4 fungi＇s respiration in the early stages. With the concentration rising up, the effectiveness increased. However, as time went on, the respiration of the mycelia treated with fungicides recovered and SHAM could not inhibit the oxygen consuming. This reaction between the mycelia and the fungicides appeared not to initiate alternative respiration but rather the other mechanism created a lack of efficacy.