EFFECT OF ANTHROPOGENIC CO_2 ON THE pH AND THE SATURATION STATES OF CALCITE AND ARAGONITE OF SEAWATER

Growth of phytoplankton, zooplankton and probably most other marine organisms as well, is likely to be affected by the pH of seawater. Growth of calcareous shells and skeletons is less likely to be affect ed by the saturation states of calcite and aragonite but the dissolution is. The increase of CO2 in the oceans due to burning of fossil fuel and clearing of forests is decreasing the pH of seawater and the degress of saturation for calcite and aragonite worldwide. This paper presents the results of the first attempt to estimate the vertical distribution of anthropogenic CO2, and the decreases in pH and the degrees of saturation of calcite and aragonite in seawater near Taiwan. Most ef fects are very small except for the possible dissolution of aragonite on the upper continental slope starting around 2050 AD.

¹³C-¹⁸O Bonds in Precipitated Calcite and Aragonite: An <i>ab Initio</i>Study

The 13C-18O bonds in carbonates are potential single-phase geo-thermometers. However, their theoretical distributions (noted as Δ47s) in CO2 degassed from calcite and aragonite with phosphoric acid are unclear. Thus, the isotope reactions of 13C-18O bonds on the growing surfaces of calcite (0001) and aragonite (001) planes were investigated using ab initio techniques. It was found that these reactions determined 13C-18O clumped isotope signatures in bulk calcite and aragonite minerals with novel Δ47 polynomials: and for temperatures ranging from 260 to 1500 K. These theoretical results were in good agreement with the experimental data. In addition, the influence of phosphoric acid on these polynomials was at the level of 0.01‰.

Coupled multiphysical model for investigation of influence factors in the application of microbially induced calcite precipitation

The study presents a comprehensive coupled thermo-bio-chemo-hydraulic(T-BCH)modeling framework for stabilizing soils using microbially induced calcite precipitation(MICP).The numerical model considers relevant multiphysics involved in MICP,such as bacterial ureolytic activities,biochemical reactions,multiphase and multicomponent transport,and alteration of the porosity and permeability.The model incorporates multiphysical coupling effects through well-established constitutive relations that connect parameters and variables from different physical fields.It was implemented in the open-source finite element code OpenGeoSys(OGS),and a semi-staggered solution strategy was designed to solve the couplings,allowing for flexible model settings.Therefore,the developed model can be easily adapted to simulate MICP applications in different scenarios.The numerical model was employed to analyze the effect of various factors,including temperature,injection strategies,and application scales.Besides,a TBCH modeling study was conducted on the laboratory-scale domain to analyze the effects of temperature on urease activity and precipitated calcium carbonate.To understand the scale dependency of MICP treatment,a large-scale heterogeneous domain was subjected to variable biochemical injection strategies.The simulations conducted at the field-scale guided the selection of an injection strategy to achieve the desired type and amount of precipitation.Additionally,the study emphasized the potential of numerical models as reliable tools for optimizing future developments in field-scale MICP treatment.The present study demonstrates the potential of this numerical framework for designing and optimizing the MICP applications in laboratory-,prototype-,and field-scale scenarios.

Flotation separation of scheelite from calcite using luteolin as a novel depressant

This paper proposes luteolin(LUT)as a novel depressant for the flotation-based separation of scheelite and calcite in a sodium oleate(NaOL)system.The suitability of LUT as a calcite depressant is confirmed through micro-flotation testing.At pH=9,with LUT concentration of 50 mg·L^(-1) and NaOL concentration of 50 mg·L^(-1),scheelite recovery reaches 80.3%.Calcite,on the other hand,exhibits a recovery rate of 17.6%,indicating a significant difference in floatability between the two minerals.Subsequently,the surface modifica-tions of scheelite and calcite following LUT treatment are characterized using adsorption capacity testing,Zeta potential analysis,Fourier transform infrared spectroscopy(FT-IR),X-ray photoelectron spectroscopy(XPS),and atomic force microscopy(AFM).The study in-vestigates the selective depressant mechanism of LUT on calcite.Adsorption capacity testing and Zeta potential analysis demonstrate sub-stantial absorption of LUT on the surface of calcite,impeding the further adsorption of sodium oleate,while its impact on scheelite is min-imal.FT-IR and XPS analyses reveal the selective adsorption of LUT onto the surface of calcite,forming strong chemisorption bonds between the hydroxyl group and calcium ions present.AFM directly illustrates the distinct adsorption densities of LUT on the two miner-al types.Consequently,LUT can effectively serve as a depressant for calcite,enabling the successful separation of scheelite and calcite.

Flotation separation of brucite and calcite in dodecylamine system enhanced by regulator potassium dihydrogen phosphate

To achieve efficient flotation separation of brucite and calcite,flotation separation experiments were conducted on two minerals using dodecylamine(DDA)as the collector and potassium dihydrogen phosphate(PDP)as the regulator.The action mechanism of DDA and PDP was explored through contact angle measurement,zeta potential detection,solution chemistry calculation,FTIR analysis,and XPS detection.The flotation results showed that when DDA dosage was 35 mg/L and PDP dosage was 40 mg/L,the maximum floating difference between brucite and calcite was 79.81%,and the selectivity separation index was 6.46.The detection analysis showed that the main dissolved component HPO_(4)^(2−)of PDP is selectively strongly adsorbed on the Ca site on the surface of calcite,promoting the adsorption of the main dissolved component RNH_(3)^(+)of DDA on calcite surface,while brucite is basically not affected by PDP.Therefore,PDP is an effective regulator for the reverse flotation separation of brucite and calcite in DDA system.

Further study on the genesis of lamellar calcite veins in lacustrine black shale--A case study of Paleogene in Dongying Depression, China

Lamellar calcite veins are prevalent in carbonate-rich,lacustrine dark shale.The formation mechanisms of these veins have been extensively debated,focusing on factors such as timing,depth,material source,and driving forces.This paper examines dark lacustrine shale lamellar calcite veins in the Paleogene strata of Dongying Depression,using various analytical techniques:petrography,isotope geochemistry,cathodoluminescence,inclusion thermometry,and electron probe micro-analysis.Two distinct types of calcite veins have been identified:granular calcite veins and sparry calcite veins.These two types differ significantly in color,grain structure,morphology,and inclusions.Through further investigation,it was observed that vein generation occurred from the shallow burial period to the maturation of organic matter,with a transition from granular calcite veins to sparry calcite veins.The granular calcite veins exhibit characteristics associated with the shallow burial period,including plastically deformed laminae and veins,the development of strawberry pyrite,the absence of oil and gas,weak fractionation in oxygen isotopes,and their contact relationship with sparry calcite veins.These granular calcite veins were likely influenced by the reduction of sulfate bacteria.On the other hand,sparry calcite veins with fibrous grains are antitaxial and closely linked to the evolution and maturation of organic matter.They contain oil and gas inclusions and show a distribution range of homogenization temperature between 90℃ and 120℃ and strong fractionation in oxygen isotopes,indicating formation during the hydrocarbon expulsion period.The carbon isotope analysis of the surrounding rocks and veins suggests that the material for vein formation originates from the shale itself,specifically authigenic micritic calcite modified by the action of methanogens.The opening of horizontal fractures and vein formation is likely driven by fluid overpressure resulting from undercompaction and hydrocarbon expulsion.Veins may form rapidly or through multi-stage composite processes.Early veins are predominantly formed in situ,while late veins are a result of continuous fluid migration and convergence.Furthermore,the veins continue to undergo modification even after formation.This study emphasizes that the formation of lamellar calcite veins in shale is a complex diagenetic process influenced by multiple factors:biology,organic matter,and inorganic processes,all operating at various stages throughout the shale's diagenetic history.

Genetic mechanism and petroleum geological significance of calcite veins in organic-rich shales of lacustrine basin:A case study of Cretaceous Qingshankou Formation in Songliao Basin,China

Based on the observation and analysis of cores and thin sections,and combined with cathodoluminescence,laser Raman,fluid inclusions,and in-situ LA-ICP-MS U-Pb dating,the genetic mechanism and petroleum geological significance of calcite veins in shales of the Cretaceous Qingshankou Formation in the Songliao Basin were investigated.Macroscopically,the calcite veins are bedding parallel,and show lenticular,S-shaped,cone-in-cone and pinnate structures.Microscopically,they can be divided into syntaxial blocky or columnar calcite veins and antitaxial fibrous calcite veins.The aqueous fluid inclusions in blocky calcite veins have a homogenization temperature of 132.5–145.1℃,the in-situ U-Pb dating age of blocky calcite veins is(69.9±5.2)Ma,suggesting that the middle maturity period of source rocks and the conventional oil formation period in the Qingshankou Formation are the sedimentary period of Mingshui Formation in Late Cretaceous.The aqueous fluid inclusions in fibrous calcite veins with the homogenization temperature of 141.2–157.4℃,yields the U-Pb age of(44.7±6.9)Ma,indicating that the middle-high maturity period of source rocks and the Gulong shale oil formation period in the Qingshankou Formation are the sedimentary period of Paleocene Yi'an Formaiton.The syntaxial blocky or columnar calcite veins were formed sensitively to the diagenetic evolution and hydrocarbon generation,mainly in three stages(fracture opening,vein-forming fluid filling,and vein growth).Tectonic extrusion activities and fluid overpressure are induction factors for the formation of fractures,and vein-forming fluid flows mainly as diffusion in a short distance.These veins generally follow a competitive growth mode.The antitaxial fibrous calcite veins were formed under the driving of the force of crystallization in a non-competitive growth environment.It is considered that the calcite veins in organic-rich shale of the Qingshankou Formation in the study area has important implications for local tectonic activities,fluid overpressure,hydrocarbon generation and expulsion,and diagenesis-hydrocarbon accumulation dating of the Songliao Basin.

Adsorption behavior of CO_(2)/H_(2)S mixtures in calcite slit nanopores for CO_(2) storage:An insight from molecular perspective

It is acknowledged that injecting CO_(2) into oil reservoirs and saline aquifers for storage is a practical and affordable method for CO_(2) sequestration.Most CO_(2) produced from industrial exhaust contains impurity gases such as H_(2)S that might impact CO_(2) sequestration due to competitive adsorption.This study makes a commendable effort to explore the adsorption behavior of CO_(2)/H_(2)S mixtures in calcite slit nanopores.Grand Canonical Monte Carlo(GCMC)simulation is employed to reveal the adsorption of CO_(2),H_(2)S as well as their binary mixtures in calcite nanopores.Results show that the increase in pressure and temperature can promote and inhibit the adsorption capacity of CO_(2) and H_(2)S in calcite nanopores,respectively.CO_(2)exhibits stronger adsorption on calcite surface than H_(2)S.Electrostatic energy plays the dominating role in the adsorption behavior.Electrostatic energy accounts for 97.11%of the CO_(2)-calcite interaction energy and 56.33%of the H_(2)S-calcite interaction energy at 10 MPa and 323.15 K.The presence of H_(2)S inhibits the CO_(2) adsorption in calcite nanopores due to competitive adsorption,and a higher mole fraction of H_(2)S leads to less CO_(2) adsorption.The quantity of CO_(2) adsorbed is lessened by approximately 33%when the mole fraction of H_(2)S reaches 0.25.CO_(2) molecules preferentially occupy the regions near the po re wall and H_(2)S molecules tend to reside at the center of nanopore even when the molar ratio of CO_(2) is low,indicating that CO_(2) has an adsorption priority on the calcite surface over H_(2)S.In addition,moisture can weaken the adsorption of both CO_(2) and H_(2)S,while CO_(2) is more affected.More interestingly,we find that pure CO_(2) is more suitable to be sequestrated in the shallower formations,i.e.,500-1500 m,whereas CO_(2)with H_(2)S impurity should be settled in the deeper reservoirs.

Characteristics,preservation mechanisms,and significance of aragonite in lacustrine shale:A case study from the Jiyang Depression,Bohai Bay Basin

Aragonite is a metastable mineral,which is easily transformed into calcite,and generally difficult to preserve in the stratum.However,large amounts of aragonites were found in the Paleogene shale of the Jiyang Depression.The characteristics and preservation mechanisms of these aragonites were analyzed through a series of analytical methods,including cathodoluminescence,field-emission scanning electron microscopy(FESEM),laser ablation inductively coupled plasma mass spectrometry(LA-ICP-MS),microarea carbon and oxygen isotopes,Sr isotopes,and dissolution simulation experiments under high temperature and high pressure.The research results show that:(1)Aragonite in the Paleogene shale of the Jiyang Depression is related to algal microbial fossils,primarily composed of coccoliths and characterized by two emission peaks at 420 nm and 480 nm in cathodoluminescence;(2)The primary factor allowing biological aragonite to be preserved is the immaturity of the organic matter and the deficiency of abundant organic acids necessary for its dissolution or transformation,which is confirmed by the evidence of organic matter maturity and simulation experiments of organic acid dissolution on aragonite under high-temperature and high-pressure conditions.Additional factors that may aid in the preservation of aragonite are the ideal sedimentation conditions,the defense of organic coating,and the enclosed environment with tiny pores,low porosity,and low permeability;(3)These aragonite-rich shales,characterized by coccolithophores,provide a solid evidence for seawater intrusion into terrestrial lake basin,and have a significant implication for the source and storage of shale oil.

Anisotropic surface broken bond properties and wettability of calcite and fluorite crystals

Anisotropic surface broken bond densities of six different surfaces of calcite and three surfaces of fluorite were calculated. In terms of the calculated results, the commonly exposed surfaces of the two minerals were predicted and the relations between surface broken bonds densities and surface energies were analyzed. Then the anisotropic wettability of the commonly exposed surfaces was studied by means of contact angle measurement. The calculation results show that the （101^-4）, （213^-4）and （01 1^-8）surfaces for calcite and （111） for fluorite are the most commonly exposed surfaces and there is a good rectilinear relation between surface broken bond density and surface energy with correlation of determination （R^2） of 0.9613 and 0.9969, respectively. The anisotropic wettability of different surfaces after immersing in distilled water and sodium oleate solutions at different concentrations can be explained by anisotropic surface broken bond densities and active Ca sites densities, respectively.

THE STUDY OF AN ALLOWABLE CALCITE SUPERSATURATION IN LOW TEMPERATURE GEOTHERMAL SYSTEMS

Two geothermal fields with calcite scaling in some wells in Iceland were selected for the study of calcite scaling potential. An allowable supersaturation was found by comparing the degree of calcite supersaturation and actual scaling status in the selected wells.The saturation index,0.37～ 0.48, was the boundary between calcite scaling and no scaling. The information about changes in chloride concentration shows that mixing different waters is the main cause to form calcite scaling in the geothermal wells selected in this study.In this case, the content of chloride can be used as an index of scaling.

REE and C-O Isotopic Geochemistry of Calcites from the World-class Huize Pb-Zn Deposits,Yunnan,China:Implications for the Ore Genesis

The world-class Huize Pb-Zn deposits of Yunnan province,in southwestern China,located in the center of the Sichuan-Yunnan-Guizhou Pb-Zn polymetallic metallogenic province,has Pb＋Zn reserves of more than 5 million tons at Pb＋Zn grade of higher than 25%and contains abundant associated metals,such as Ag,Ge,Cd,and Ga.The deposits are hosted in the Lower Carboniferous carbonate strata and the Permian Emeishan basalts which distributed in the northern and southwestern parts of the orefield.Calcite is the only gangue mineral in the primary ores of the deposits and can be classified into three types,namely lumpy,patch and vein calcites in accordance with their occurrence.There is not intercalated contact between calcite and ore minerals and among the three types of calcite,indicating that they are the same ore-forming age with different stages and its forming sequence is from lumpy to patch to vein calcites. This paper presents the rare earth element（REE） and C-O isotopic compositions of calcites in the Huize Pb-Zn deposits.From lumpy to patch to vein calcites,REE contents decrease as LREE/ HREE ratios increase.The chondrite-normalized REE patterns of the three types of calcites are characterized by LREE-rich shaped,in which the lumpy calcite shows（La）_N〈（Ce）_N〈（Pr）_N≈（Nd）_N with Eu/Eu~＊〈1,the patch calcite has（La）_N〈（Ce）_N〈（Pr）_N≈（Nd）_N with Eu/Eu~＊〉1,and the vein calcite displays（La）_N〉（Ce）_N〉（Pr）_N〉（Nd）_N with Eu/Eu~＊〉1.The REE geochemistry of the three types of calcite is different from those of the strata of various age and Permian Emeishan basalt exposed in the orefield.Theδ^（13） C_（PDb） andδ^（18）O_（Smow） values of the three types of calcites vary from-3.5‰to-2.1‰and 16.7‰to 18.6‰,respectively,falling within a small field between primary mantle and marine carbonate in theδ^（13）C_（PDb） vsδ^（18）O_（Smow） diagram. Various lines of evidence demonstrate that the three types of calcites in the deposits are produced from the same source with different stages.The ore-forming fluids of the deposits resulted from crustal -mantle mixing processes,in which the mantle-derived fluid components might be formed from degassing of mantle or/and magmatism of the Permian Emeishan basalts,and the crustal fluid was mainly provided by carbonate strata in the orefield.The ore-forming fluids in the deposits were homogenized before mineralization,and the ore-forming environment varied from relatively reducing to oxidizing.

Calcite Dissolution in Deionized Water from 50℃ to 250℃ at 10 MPa:Rate Equation and Reaction Order

Carbonate minerals and water （or geofluids） reactions are important for modeling of geochemical processes and have received considerable attention over the past decades. The calcite dissolution rates from 50℃ to 250℃ at 10 MPa in deionized water with a flow rate varying from 0.2 to 5 mL/min were experimentally measured in a continuous flow column pressure vessel reactor. The dissolution began near the equilibrium with c/ceq 〉 0.3 and finally reached the equilibrium at 100℃-250℃, so the corresponding solubility was also determined as 1.87, 2.02, 2.02 and 1.88×10^-4.mol/L at 100℃, 150℃, 200℃ and 250℃ respectively, which was first increasing and then switching to decreasing with temperature and the maximum value might occur between 150℃ and 200℃. The experimental dissolution rate not only increased with temperature, but also had a rapid increase between 150℃ and 200℃ at a constant flow rate of 4 mL/min. The measured dissolution rates can be described using rate equations of R = k（1-c/ceq）n or R = kc-n. In these equations the reaction order n changed with temperature, which indicates that n was a variable rather than a constant, and the activation energy was 13.4 kJ/mol calculated with R = k（1-c/ceq）n or 18.0 kJ/mol with R = kc^-n, which is a little lower than the surface controlled values. The varied reaction order and lower activation energy indicates that calcite dissolution in this study is a complex interplay of diffusion controlled and surface controlled processes.

Molecular dynamics simulation of adsorption of an oil-water-surfactant mixture on calcite surface

An interface super molecular structure model for oil-water-surfactant mixture and calcite was established. By using a molecular dynamics method, the effects of rhamnolipid, sodium dodecyl benzene sulfonate and sodium hexadecyl sulfonate on the interface adsorption behavior of oil molecules were investigated. It was found that these three surfactants could reduce oil-calcite interface binding energy, and play a role of oil-displacing agent.

Existence and release of fluid inclusions in bornite and its associated quartz and calcite

The existence and release of fluid inclusions in bornite and its associated minerals, namely, quartz and calcite were investigated and confirmed. The structures, forms, and phases of these large quantities of fluid inclusions were also studied. A mass of fluid inclusions with various sizes, distributions, shapes, and phases exist in bornite and its associated minerals. Their sizes vary from a few micrometers to tens of micrometers, and the forms appear as negative crystals, or elongated, elliptical, and irregular. At room temperature, fluid inclusions were mainly characterized as gas-liquid two- phase. However, small amounts of fluid inclusions with pure gas phase and pure liquid single-phase were also observed in quartz and calcite. These fluid inclusions initially broke during the ore crushing and grinding process and then released into the flotation pulp in the flotation process. The quantitative analysis of fluid inclusions in the solution and the comparisons of mineral dissolution show that the amount of copper and iron released by fluid inclusions in the bornite sample is higher than the amount dissolved by the mineral; fluid inclusions in the associated gangue minerals, quartz, and calcite also make contribution.

Quantifying the carbon source of pedogenic calcite veins in weathered limestone: implications for the terrestrial carbon cycle

The continent is the second largest carbon sink on Earth’s surface.With the diversification of vascular land plants in the late Paleozoic,terrestrial organic carbon burial is represented by massive coal formation,while the development of soil profiles would account for both organic and inorganic carbon burial.As compared with soil organic carbon,inorganic carbon burial,collectively known as the soil carbonate,would have a greater impact on the long-term carbon cycle.Soil carbonate would have multiple carbon sources,including dissolution of host calcareous rocks,dissolved inorganic carbon from freshwater,and oxidation of organic matter,but the host calcareous rock dissolution would not cause atmospheric CO2drawdown.Thus,to evaluate the potential effect of soil carbonate formation on the atmospheric p CO2level,different carbon sources of soil carbonate should be quantitatively differentiated.In this study,we analyzed the carbon and magnesium isotopes of pedogenic calcite veins developed in a heavily weathered outcrop,consisting of limestone of the early Paleogene Guanzhuang Group in North China.Based on the C and Mg isotope data,we developed a numerical model to quantify the carbon source of calcite veins.The modeling results indicate that4–37 wt%of carbon in these calcite veins was derived from atmospheric CO2.The low contribution from atmospheric CO2might be attributed to the host limestone that might have diluted the atmospheric CO2sink.Nevertheless,taking this value into consideration,it is estimated that soil carbonate formation would lower 1 ppm atmospheric CO2within 2000 years,i.e.,soil carbonate alone would sequester all atmospheric CO2within 1 million years.Finally,our study suggests the C–Mg isotope system might be a better tool in quantifying the carbon source of soil carbonate.

A novel green depressant for flotation separation of scheelite from calcite

Polyaspartic acid(PASP)was used as a novel environmental-friendly depressant,and its inhibition effect on flotation performance of scheelite and calcite using sodium oleate(NaOL)as a collector was investigated by ways of flotation experiments,zeta potential measurement,contact angle measurement and infrared spectroscopic analysis(IR).The results show that PASP exhibits stronger inhibition capability and selectivity than acidified water glass,and the flotation separation of scheelite from calcite can be realized in the presence of 6 mg/L PASP and 20 mg/L NaOL at pH>6.In the presence of PASP,the zeta potential of calcite surface almost keeps unchanged after adding NaOL,and the contact angle decreases sharply.Therefore,it is indicated that PASP significantly decreases the adsorption of NaOL on calcite surface.By contrast,it has no distinct effect on the adsorption of NaOL on the scheelite surface,which is further confirmed by IR results.

Adsorption of octanohydroxamic acid at fluorite surface in presence of calcite species

The surface properties of fluorite are often affected by dissolved gangue species(e.g.,calcite)during the flotation process.Microflotation testing with and without the addition of calcite supernatant was conducted using octanohydroxamic acid(OHA)as the collector.The results revealed that dissolved calcite species significantly affected the flotation behavior of fluorite.Fourier transform infrared spectra confirmed that the decrease in flotation recovery was linked to lower OHA adsorption.Solution chemistry analysis indicated that CaCO_(3) and Ca^(2+)from the calcite supernatant were the most favorably adsorbed species,and X-ray photoelectron spectroscopy analysis confirmed the surface adsorption of calcite species.Density functional theory simulations provided a detailed analysis of the multidentate adsorption configuration of OHA,which was the most favorable for adsorption on the fluorite surface.The adsorption energy calculation showed that the calcite dissolved species were more stably adsorbed on the fluorite surface than OHA.The pre-adsorption of calcite dissolved species hindered the adsorption of OHA due to electrostatic repulsion.

Effects of sodium carbonate and calcium chloride on calcite depression in cationic flotation of pyrolusite

In the cationic flotation of pyrolusite using dodecyl ammine(DDA),the depressive effect of sodium carbonate andcalcium chloride on the calcite mineral was investigated systematically through flotation experiments,FTIR analysis,contact anglemeasurements and zeta potential tests.The microflotation experiments showed that both depressant agents decrease the flotationrecovery of calcite significantly.In addition,sodium carbonate acts as activator agent for pyrolusite,and increases its floatability.Theflotation experiments and contact angle measurements indicated that the selective depression effect of sodium carbonate on thecalcite mineral is more than that of calcium chloride.As evidenced by zeta potential and FT-IR analysis,sodium carbonate decreasesthe negative charges on the surface of calcite mineral and subsequently reduces the adsorption of DDA collector through electrostaticforces.At a pH of7.5,using2000g/t DDA and1500g/t sodium carbonate,a pyrolusite concentrate containing almost40%MnOwith71.5%recovery is achieved by carrying out the ore flotation experiments on the tabling pre-concentrate.

Selective flotation of smithsonite, quartz and calcite using alkyl diamine ether as collector

The flotation separation of smithsonite from calcite and quartz using a alkyl diamine ether(GE-609)as the collector was investigated through micro-flotation experiments and the real ore flotation experiments.The results show that GE-609exhibits good collecting capability to three minerals without selectivity.The presence of sodium sulfide enhances the flotation of smithsonite and calcite while inhibits quartz.Moreover,both sodium silicate and sodium hexametaphosphate exhibit good selective inhibition to calcite.The real ore test results show that a zinc concentrate containing23.51%Zn with the recovery of71.02%is obtained in the closed-circuit test.To understand the adsorption of GE-609on smithsonite surface,zeta potential measurement and FTIR analysis were carried out,and the results indicate that the collector GE-609can adsorb on smithsonite surface through both electrostatic adsorption and chemical adsorption,and the presence of sodium sulfide enhances the adsorption of GE-609.