Sequential Extraction of Aluminum and Iron from Acidic Soils by Chemical Selective Dissolution Methods

Potassium chloride, Na-pyrophosphate, CuCl2, NH4-oxalate, dithionite-citrate-bicarbonate (DCB) and Na-citrate solutions were employed to extract aluminum (Al) and iron (Fe) sequentially and separately from 15 acidic soils located at the Mangshan Mountains, Hunan Province, China. Many evidences showed that separate pyrophosphate extracted mainly KCI-extractable Al, organo-Al complexes and some inorganic Al compounds, whereas separate CuCl2 extracted KCl-extractable Al and some organo-Al complexes. CuCl2 extracted much less amounts of Al than pyrophosphate did from the soils. Separate oxalate did not extract all KCl-Pyrophosphate- CuCl2 -oxalate sequentially extractable Al and Fe. Also, separate DCB did not extract all KCl- pyrophosphate- CuCl2 -oxalate- DCB sequentially extractable Al. The forms of Al extracted by oxalate and DCB from the soils were majorly noncrystalline. The interlayered materials of 1.4-nm intergrade minerals of the soils were attributed mainly to hydroxy Al polymers.

Selective dissolution of eodiagenesis cements and its impact on the quality evolution of reservoirs in the Xing＇anling Group,Suderte Oil Field, Hailar Basin, China

Reservoirs in the Xing＇anling Group in the Suderte Oil Field,Hailar Basin exhibit ultra-low to low permeability and high tuffaceous material content.This study comprehensively analyzed diagenesis and quality evolution of these low-permeability reservoirs using thin sections,SEM samples,rock physical properties,pore water data,as well as geochemical numerical simulations.Calcite and analcite are the two main types of cements precipitated in the eodiagenetic stage at shallow burial depths in the reservoirs.These two cements occupied significant primary intergranular pores and effectively retarded deep burial compaction.Petrography textures suggest selective dissolution of massive analcite and little dissolution of calcite in the mesodiagenetic stage.Chemical calculations utilizing the Geochemist＇s Workbench 9.0indicated that the equilibrium constant of the calcite leaching reaction is significantly smaller than that of the analcite leaching reaction,resulting in extensive dissolution of analcite rather than calcite in the geochemical system with both minerals present.Numerical simulations with constraints of kinetics and pore water chemistry demonstrated that the pore water in the Xing＇anling group is saturated with respect to calcite,but undersaturated with analcite,leading to dissolution of large amounts of analcite and no dissolution of calcite.Significant secondary intergranular pores have formed in analcite-cemented reservoirs from selective dissolution of analcite in the mesodiagenetic stage;the analcite dissolution formed preferential flow paths in the reservoirs,which promoted feldspar dissolution;and dissolution of such minerals led to the present reservoirs with medium porosity and low permeability.Calcite-cemented tight reservoirs have not experienced extensive dissolution of cements,so they exhibit ultra-low porosity and permeability.

Ultrasound application in alkaline pretreatment process of spodumene to improve particle floatability

Selective surface dissolution was found to be important in spodumene flotation. In this study, we proposed to introduce ultrasound into the pretreatment process to accelerate particle vibration and cavitation, as well as the migration of mineral surface components to solution. Micro-flotation results showed that the flotation recovery of spodumene can be 86.08% by ultrasound pretreatment, but only 39.30% by traditional mechanical agitation pretreatment. Compared with traditional mechanical agitation, ultrasonic pretreatment can shorten the pretreatment process, reduce the dosage of agents, reduce the mechanical agitation speed, and improve the efficiency of the pretreating process. Inductively coupled plasma analysis showed that, in the ultrasonic system, the amount of Li, Al, and Si species in the solution was twice as much as those in the traditional preprocessing system. Moreover, the scanning electron microscope results demonstrated a larger surface dissolution area in the ultrasonic system. X-Ray photoelectron spectroscopy results showed that the atomic concentration of Si species on the spodumene surface decreased, whereas the relative atomic concentrations of Li and Al species increased, indicating that the ultrasound effect strengthened the selective dissolution of elements on the mineral surface.The high-resolution spectra of O 1s showed that more collectors are adsorbed on the mineral surface treated by ultrasonic pretreatment.

Selective recovery of Sn from copper alloy dross and its heat-treatment for synthesis of SnO_2

Preliminary study on concentration and separation of tin(Sn) from copper alloy dross by selective dissolution method was conducted. The tin in the copper alloy dross did not dissolve in an aqueous nitric acid solution which could allow separation of tin from the copper alloy dross. The tin as H2SnO3(metastannic acid) phase was precipitated in the solution with centrifuging process and transformed to tin dioxide(SnO2) after drying process. The dried sample was heat-treated at low temperature and its phase characteristics, surface morphology and chemical composition were investigated.

Employing magnesium−lead melt for synergetic and selective extraction of copper from copper−cobalt alloy

This research aims to extract Cu from Cu-Co alloy with high efficiency and selectivity by employing binary Mg-Pb melt. The optimal conditions for the extraction of Cu were determined. The results showed under optimal conditions, 96.5% of Cu in the Cu-Co alloy could be selectively extracted after treatment at 800 ℃ for 1 h, with the extraction rates of only 0.2% Fe, 0.6% Co, and 1.4% Si. The dissolution mechanism involved the counter diffusion of Mg/Pb and Cu across the diffusion zone of the Cu-Co alloy, and Mg in the binary Mg-Pb melt played a major role in the selective dissolution of Cu, especially at the dissolution forefront. The rate-controlling step of the extraction was dominated by the interfacial reaction.

Factors Controlling the Distribution of Transitional Metal Elements in Marine Hydrogenic Ferromanganese Crusts

A series of selective dissolution experunents were conducted on the hydrogeinc ferromanganese crusts collected near Line Island to study the geochemistry of Mn, Fe, Cu, Co, Ni and Ti. Despite of the fact that the very close intergrowth between amorphous ferric oxyhydroxides and 6-MnO2 exists in the hydrogenic ferromanganese crusts, there is no isomorphous substitution between iron and manganese. This is because the two elements in oxides have different crystal chemistry and geochemistry, such assertion bemg in agreement with the results of selective dissolution experiments. Transitional metal elements such as Cu, Co, Ni and Ti are enriched in different phases, i.e. Ni and Co are incorporated into 6-MnO2 while Cu and Ti are incorporated into ferric oxyhy- droxides. The distributions of the elements in amorphous ferric oxyhydroxides and δ-MnO2 are controlled by the existing states of the elements in the seawater and the crystal chemistry and geochemistry of these elements/inns in oxides.

Selective dissolution to synthesize densely populated Pt single atom catalyst

Single atom catalysts(SACs)have become one of research focuses in heterogeneous catalysis for their effective utilization of active metal atoms and unique properties in various catalytic reactions.However,due to their high surface energy,noble metal single atoms like Pt tend to migrate and agglomerate to form larger clusters or nanoparticles,which makes it a challenge to fabricate noble metal SACs with high loading(>5 wt.%).Furthermore,the decisive factors of loading maximum are still not clear.Here,we reported a manganese oxide supported Pt SAC with a high loading of 5.6 wt.%synthesized by selective dissolution strategy.The pre-stabilization of Pt by coordinated oxygen and the abundant surface defects of support are the determinants of high loading.The Pt SAC exhibited much better H_(2)spill-over and hydrocarbon oxidation abilities with lower adsorption and dissociation energies than the manganese oxide support because of its local electronic structure with less repulsion.

Quantitative Determination of Composition of Quaternary Cementitious Materials

Based on the principle of ENV 196-4 ＂Methods of testing cement - Part 4 Quantitative determination of constituents or Chinese Standard GB/12960-2007 Quantitative measurement of mineral admixtures in cement, methods were developed for quantitative determination of fly ash, slag and limestone powder in fresh cement pastes, mortars and concretes. Limestone powder was determined using thermal analysis method. The residue content of fly ash on an 80um sieve, and silt contents of aggregate were also considered during the quantitative determination of mineral composition of quaternary cementitious system. With the developed methods, the deviations between the measured and the actual mineral contents of the constituent in the eemantitious material in fresh cement paste, mortar and concrete, were within 3%.

Electrocatalytic oxygen reduction performances of surface Ag granular packs electrodeposited from dual-phase Ag_(35.5)Zn_(64.5) precursor alloys by triangle wave potential cycling

Surface Ag granular packs(SAgPs) have been fabricated from dual-phase Ag_(35.5)Zn_(64.5) precursor alloy consisting of both e and c phases by using a facile one-step triangle wave potential cycling in 0.5 mol·L^(-1) KOH.During the continuous potential cyclic sweeping, the c phases preferentially dissolve during the anodic scan and dominant reduction reactions of Ag cations lead to redeposition and accumulation of Ag atoms together to form SAg Ps during cathodic scan. The e phases stay inactive to form a continuous skeleton in the inner regions. SAg Ps with an average particle size of 94-129 nm can be obtained at scan rates of 25, 50 and 100 mV·s^(-1) for 100 triangle wave potential cycles. SAgPs formed at a scan rate of 50 mV·s^(-1) exhibit superior oxygen reduction reaction performances with the onset potential of 0.93 V, half-wave potential of 0.72 V and an electron transfer number of 4.0.The above-mentioned SAgPs have superior stabilities as ORR catalysts.

Efficient nanostructured heterogeneous catalysts by electrochemical etching of partially crystallized Fe-based metallic glass ribbons

Although an increasing interest has been attracted to further develop heterostructured catalysts from metallic glasses(MGs) by heat treatment, overcoming surface oxidation effect is still a critical problem for such environmental catalysts. Herein, a short-time electrochemical etching of partially crystallized Febased ribbons in 0.3 M H3 PO4 electrolyte enables the formation of honeycomb-like nanoporous structure as effective catalytic active sites in Fenton-like process. Studies of structure and surface morphologies reveal that the formation of nanoporous structure by potentiostatic etching originates from electrochemical potential difference of nanocrystals(a-Fe(Si) and Fe2 B) and residual amorphous phase in partially crystallized ribbons, where Fe2 B having a lower open circuit potential tends to be selectively dissolved.Simultaneously, thin oxide layer after electrochemical etching exposes more active sites for H2 O2 activation and provides an effective protection of nanocrystals from massive loss during etching. Investigation of optimal processing conditions suggests that the selection of electrolyte plays an important role;dye degradation rates of etched ribbons in HNO3 and Na2 SO4 electrolytes can also achieve at least 2 times higher than that of as-annealed ribbons. This work holds the promise to develop novel environmental catalysts by effective electrochemical etching of partially crystallized ribbons.