Adsorption characteristics of Pb(Ⅱ)ions on sulfidized hemimorphite surface under ammonium sulfate system

In this work,the effect of ammonium sulfate on the adsorption characteristics of low-concentration Pb(Ⅱ)ions on the sulfidized hemimorphite surface was comprehensively investigated.The results showed that ammonium sulfate could increase the maximum recovery of hemimorphite from 69.42%to 88.24%under a low concentration of Pb(Ⅱ)ions.On the hemimorphite surface pretreated with ammonium sulfate,the adsorption of Pb(Ⅱ)ions was enhanced and the main species of Pb adsorbed was changed from Pb―O/OH to PbS.This was due to the larger amount of ZnS providing more effective adsorption sites for Pb components to generate Pb S.Meanwhile,the intensity of ZnS decreased with the formation of PbS,demonstrating that ZnS was covered by PbS which formed later on the mineral surface.It was beneficial for the adsorption of butyl xanthate on the hemimorphite surface to form more hydrophobic substances.As a result,ammonium sulfate played a crucial role in realizing the efficient recovery of hemimorphite.

Effect of ammonium sulfate on the formation of zinc sulfide species on hemimorphite surface and its role in sulfidation flotation

Effectively strengthening the surface sulfidation is essential for recovering hemimorphite by froth flotation.In this work,inductively coupled plasma optical emission spectrometer(ICP-OES)measurements,Visual MINTEQ calculation,X-ray photoelectron spectroscopy(XPS)analysis,time of flight secondary ion mass spectrometry(ToF-SIMS)analysis,and micro-flotation experiments were explored to systematically investigate the effect of ammonium sulfate((NH_(4))_(2)SO_(4))on the formation of zinc sulfide species on hemimorphite surface and its role in sulfidation flotation.The results showed that(NH_(4))_(2)SO_(4)exhibited a positive influence on hemimorphite sulfidation flotation.It was ascribed to the number of zinc components in the form of Zn^(2+)and[Zn(NH_(3))_(i)]^(2+)(i=1–4)increased in the flotation system after hemimorphite treatment with(NH_(4))_(2)SO_(4),which was beneficial to its interaction with sulfur species in solution,resulting in a dense and stable zinc sulfide layer generated on the hemimorphite surface.[Zn(NH_(3))_(i)]^(2+)participated in the sulfidation reaction of hemimorphite as a transition state.In addition the sulfidation reaction of hemimorphite was accelerated by(NH_(4))_(2)SO_(4).Thus,(NH_(4))_(2)SO_(4)presents a vital role in promoting the sulfidation of hemimorphite.

Extraction of alumina from fly ash by ammonium hydrogen sulfate roasting technology

NH4HSO4 roasting technology was used for preparing Al2O3 from fly ash. First, Al and Fe were extracted from fly ash by NH4HSO4 roasting and deionized water leaching. Then, the Al and Fe in the leached liquid were precipitated by adding NH4HCO3 solution. After the mixed precipitations of Al（OH）3 and Fe（OH）3 were leached by NaOH solution, the NaAl（OH）4 solution was decomposed by carbonation. Finally, the pure Al（OH）3 was calcined to α-Al2O3. The optimal conditions of the whole technology were determined by experiments. The quality ofa-Al2O3 product is up to the technical indicator of YS/T 274-1998 standard.

Study on the Acute Toxicity of Rare Earth Yttrium to Earthworms under the Stress of Leaching Agent Ammonium Sulfate

This study aimed to investigate the toxicity of rare earth ion yttrium under the stress of leaching agent ammonium sulfate （NH4）2SO4. [Method] By using earthworms as indicator organisms of environmental pol ution, acute toxic ef-fects of rare earth yttrium on earthworms under the stress of ammonium sulfate were investigated with filter paper contact method. [Result] Under single stress of rare earth yttrium, the semi-lethal concentration after 48 and 24 h was LC50=213.41 mg/L and LC50=322.63 mg/L, respectively. ② Under single stress of ammonium sul-fate, the semi-lethal concentration after 48 h and 24 h was LC50=13.89 g/L and LC50=15.05 g/L, respectively. ③ In combined treatment of low concentration （10 g/L） of ammonium sulfate and different doses of rare earth yttrium, the semi-lethal con-centration after 48 and 24 h was LC50=198.65 g/L and LC50=399.85 g/L, respective-ly; in combined treatment of middle concentration （14 g/L） of ammonium sulfate and different doses of rare earth yttrium, the semi-lethal concentration after 48 and 24 h was LC50=167.3 mg/L and LC50=256.73 mg/L, respectively; in combined treatment of high concentration （20 g/L） of ammonium sulfate and different doses of rare earth yttrium, the semi-lethal concentration after 48 h and 24 h was LC50=31.03 mg/L and LC50=127.65 mg/L, respectively. [Conclusion] Low concentration of ammonium sulfate could reduce the toxicity of rare earth yttrium to earthworms and produce certain antagonism against rare earth yttrium; middle concentration ammonium sulfate in-creased the toxicity of rare earth yttrium to earthworms and produced relatively sig-nificant synergistic effects; high concentration ammonium sulfate significantly in-creased the toxicity of rare earth yttrium to earthworms. Compared with ammonium sulfate, dead earthworms exposed to rare earth yttrium were more easily fractured, and living earthworms showed insensitive response to acupuncture.

Solubility of hemimorphite in ammonium sulfate solution at 25 °C

The solubility of natural hemimorphite in ammonium sulfate solution was measured by isothermal solution method at 25 °C and the dissolved residue of hemimorphite was investigated by X-ray powder diffraction （XRD）, scanning electron microscopy （SEM） and Fourier transform infrared spectroscopy （FTIR） methods. The results show that zinc and silica in hemimorphite simultaneously dissolve in ammonium sulfate solution. The solubility of zinc in solution increases rapidly from 4.5381 mmol/kg in 0.5469 mol/kg ammonium sulfate solution to 11.5083 mmol/kg in 3.7038 mol/kg ammonium sulfate solution. The solubility of silica in solution increases slowly from 2.5509 mmol/kg in 0.5469 mol/kg ammonium sulfate solution to 7.2891 mmol/kg in 3.7038 mol/kg ammonium sulfate solution. The dissolved residue is the characteristic of hemimorphite Zn4Si2O7（OH）2·H2O based on the results of the XRD, SEM and FTIR. Thus, no phase transition occurs in the dissolution process of hemimorphite in ammonium sulfate solution.

Thermodynamics and kinetics of extracting zinc from zinc oxide ore by the ammonium sulfate roasting method

Thermodynamic analyses and kinetic studies were performed on zinc oxide ore treatment by （NH4）2SO4 roasting technology. The results show that it is theoretically feasible to realize a roasting reaction between the zinc oxide ore and （NH4）2SO4 in a temperature range of 573-723 K. The effects of reaction temperature and particle size on the extraction rate of zinc were also examined. It is found that a surface chemical reaction is the rate-controlling step in roasting kinetics. The calculated activation energy of this process is about 45.57 kJ/mol, and the kinetic model can be expressed as follows： 1 - （1 - α）1/3 = 30.85 exp（-45.57/RT）·t. An extraction ratio of zinc as high as 92% could be achieved under the optimum conditions.

Recovery of valuable metals from a low-grade nickel ore using an ammonium sulfate roasting-leaching process

Metal leaching from a low-grade nickel ore was investigated using an ammonium sulfate roasting-water leaching process. The nickel ore was mixed with ammonium sulfate, followed by roasting and finally leaching with water. During the process the effects of the amotmt of ammonium sulfate, roasting temperature, and roasting time on the leaching recovery of metal elements were analyzed. The optimum technological parameters were determined as follows： ammonium sulfate/ore ratio, 0.8 g/g; roasting temperature, 400℃; and roasting time, 2 h. Under the optimum condition the leaching recoveries ofNi, Cu, Fe, and Mg were 83.48%, 76.24%, 56.43%, and 62.15%, respectively. Furthermore, the dissolution kinetics of Ni and Mg from the nickel ore was studied. The apparent activation energies for the leaching reaction of Ni and Mg were 18.782 and 10.038 kJ.mo1-1, which were consistent with the values of diffusion control reactions. Therefore, the results demonstrated that the leaching recoveries of Ni and Mg were controlled by diffusion.

Thermodynamics and kinetics of alumina extraction from fly ash using an ammonium hydrogen sulfate roasting method

A novel method was developed for extracting alumina （Al2O3） from fly ash using an ammonium hydrogen sulfate （NH4HSO4） roasting process, and the thermodynamics and kinetics of this method were investigated. The thermodynamic results were verified experi-mentally. Thermodynamic calculations show that mullite present in the fly ash can react with NH4HSO4 in the 298-723 K range. Process op-timization reveals that the extraction rate can reach up to 90.95% when the fly ash reacts with NH4HSO4 at a 1：8 mole ratio of Al2O3/NH4HSO4 at 673 K for 60 min. Kinetic analysis indicates that the NH4HSO4 roasting process follows the shrinking unreacted core model, and inner diffusion through the product layer is the rate-controlling step. The activation energy is calculated to be 16.627 kJ/mol;and the kinetic equation can be expressed as 1-（2/3）α-（1-α）2/3=0.0374t exp[-16627/（RT）], whereαis the extraction rate and t is the roasting temperature.

Effect of Temperature on Phase and Alumina Extraction Efficiency of the Product from Sintering Coal Fly Ash with Ammonium Sulfate

A new developed technology for extracting alumina from coal fly ash was studied in this paper. In this technology, coal fly ash is first sintered with ammonium sulfate, forming ammonium aluminum sulfate in the resultant product, where alumina can be easily leached without using any strong acid or alkali. The products obtained under different sintering conditions were characterized by X-ray diffractometry. Alumina extraction efficiency of these products was also investigated. The results show that the sintering temperature and time substantially influence the phase composition and alumina extraction efficiency of sintered products, while the heating rate has little influence. The optimal sintering condition is 400 °C for 3 h in air with a heating rate of 6 °C·min-1.Under the optimal sintering condition, the alumina extraction efficiency from as-sintered coal fly ash can reach 85% or more.

Joint enhancement of lead accumulation in Brassica plants by EDTA and ammonium sulfate in sand culture

When EDTA was added alone in the Pb\|contaminated sand, the plant biomass and the total Pb amount in plant decreased in both species, Brassica pekinensis and B. juncea var. multiceps, though the shoot Pb amount increased. In contrast, when (NH 4) 2SO 4 was added alone in the Pb\|contaminated sand, little effect was observed on the shoot Pb amount, though the root Pb amount was significantly increased in B. juncea var. multiceps. When amending EDTA and (NH 4) 2SO 4 in combination, however, the shoot Pb amount in both species substantially increased, being, on an average, 2 times and 9 times higher than that in EDTA alone or (NH 4) 2SO 4 alone amended treatment, respectively. The two amendments showed antagonism for plant growth, but synergism for Pb bioaccumulation. B. pekinensis showed its highest level of shoot and total Pb amount in the treatment amended with EDTA and (NH 4) 2SO 4 only a half as much as in the other treatments. It is inferred that the mechanisms responsible for the joint\|enhanced Pb accumulation might be concerned with the acidification of the growth medium, cation exchange reaction and relieving EDTA induced toxicity as results by amending ammonium sulfate.

Extraction of valuable metals from Ti-bearing blast furnace slag using ammonium sulfate pressurized pyrolysis−acid leaching processes

A novel method of extracting valuable metals from Ti-bearing blast furnace slag(TBBF slag)via pressure pyrolysis of recyclable ammonium sulfate(AS)−acid leaching process was proposed.The results show that when pressurized roasting at an AS-to-slag mass ratio 3:1 and 370℃for 90 min,the extraction rates of titanium,aluminum and magnesium reached 94.5%,91.9%and 97.4%,respectively.The acid leaching solution was subjected to re-crystallization in a boiling state to obtain a titanium product having a TiO2 content of 94.1%.The above crystallization mother liquor was adjusted to pH=6 and pH≥12.2,respectively,and then qualified Al2O3 and MgO products were obtained.The analysis through XRD and SEM−EDS proves that the main phases in roasted samples were NH4AlSO4,CaSO4 and TiOSO4.The thermodynamic analysis presents that the main minerals of perovskite,spinel and diopside in raw ore could spontaneously react with the intermediate produced by AS under optimal conditions.

Atmospheric Corrosion of Steel A3 Deposited with Ammonium Sulfate and in the Presence of Sulfur Dioxide

A laboratory study of the atmospheric corrosion of carbon steel deposited with (NH4)2SO4 in the presence of SO2 is reported. The different levels of (NH4)2SO4 (0, 15, 30, 45, 60 μg·cm-2) were added on the surface of the samples before the exposure. The corrosion was investigated by a combination of gravimetry, Fourier transform infrared spectroscope and scanning electron microscopy. A detailed knowledge about the corrosion products was acquired, both quantitatively and qualitatively. The results show that the metal loss increased and the increasing tendency of corrosion rates slowed down with the increasing exposure time. The phase constituents of the corrosion products are mainly α-FeO(OH), γ-FeO(OH), and δ-FeO(OH).

Separation and recovery of Ni from copper electrolyte by crystallization of nickel ammonium sulfate double salt

The separation and recovery of Ni from the copper electrolyte by crystallization of nickel ammonium sulfate double salt were studied.It is found that the solubility of copper sulfate at the same temperature is less than that of nickel sulfate,while the solubility of copper ammonium sulfate is greater than that of nickel ammonium sulfate.So,by adding(NH_(4))_(2)SO_(4),the Ni can be selectively crystallized from the copper electrolyte.By adding(NH_(4))_(2)SO_(4)at the molar ratio of(NH_(4))_(2)SO_(4)/NiSO_(4)≤0.8,and crystallizing at−15℃for 10 h,the Ni in the copper electrolyte can be crystallized in the form of Ni(NH_(4))_(2)(SO_(4))_(2)×6H_(2)O.The qualified product of NiSO_(4)×6H_(2)O can be obtained by pyrolyzing the crystals,dissolving the pyrolysis product in water,and then concentrating the dissolved solution for crystallization.The method of double salt crystallization is a clean,environmentally-friendly,cost-effective and efficient method for separating and recovering nickel from copper electrolyte.

Role of ammonium sulfate in sulfurization flotation of azurite:Inhibiting the formation of copper sulfide colloid and its mechanism

In this study,the role of(NH_(4))_(2)SO_(4)during the sulfurization of azurite and its response to flotation were investigated.The flotation results showed that adding(NH_(4))_(2)SO_(4)prior to sulfurization decreased the formation of colloid in flotation pulp,and the floatability of the suppressed azurite caused by excess sodium sulfide was restored.After adding(NH_(4))_(2)SO_(4)prior to sulfurization,the formation of Cu(NH_(3))_(n) ^(2+)intermediate products changed the path of the sulfurization reaction,which slowed the direct impact of HSon the azurite surface.The nucleation rate was reduced,and the growth of copper sulfide crystal was improved.Covellite(syn,CuS)with larger crystal grains was formed on the azurite surface,thereby enhancing the mechanical stability of copper sulfide products onto the mineral surface.Therefore,the generated copper sulfide colloid significantly reduced,ultimately promoting the effective adsorption of xanthate on the azurite surface.

Recovery of valuable metals from waste diamond cutters through ammonia–ammonium sulfate leaching

Copper and zinc were recovered from waste diamond cutters through leaching with an ammonia–ammonium sulfate system and air as an oxidant. The effects of experimental parameters on the leaching process were investigated, and the potential–pH(E–pH) diagrams of Cu–NH_3–SO_4^(2-)–H_2O and Zn–NH_3–SO_4^(-2)–H_2O at 25°C were drawn. Results showed that the optimal parameters for the leaching reaction are as follows: reaction temperature, 45°C; leaching duration, 3 h; liquid-to-solid ratio, 50:1(mL/g); stirring speed, 200 r/min; ammonia concentration, 4.0 mol/L; ammonium sulfate concentration, 1.0 mol/L; and air flow rate, 0.2 L/min. The results of the kinetics study indicated that the leaching is controlled by the surface chemical reaction at temperatures below 35°C, and the leaching is controlled by diffusion through the product layer at temperatures above 35°C.

Extraction of Caprolactam from Aqueous Ammonium Sulfate Solution in Pulsed Packed Column Using 250Y Mellapak Packings

Liquid-liquid equilibrium (LLE) data of water-caprolactam-benzene-(NH4)2SO4 system at 303 K were measured for extraction of caprolactam from aqueous ammonium sulfate solution. The influence of fluid flow rate, pulsation intensity on flooding velocity and mass transfer was studied for extraction of caprolactam from ammonium sulfate solution in a laboratory pulsed packed column. The flooding velocities and overall apparent height of a transfer unit were given under various operation conditions. An industrial column developed based on above study is operated well. The scale-up effect is discussed.

Reaction behavior of silicon-rich diasporic bauxite with ammonium sulfate during roasting

The separation of Al from the silicon-rich diasporic bauxite is of great significance in alumina production.Herein,we proposed a low-temperature ammonium sulfate roasting-water leaching process to extract aluminum from silicon-rich diasporic bauxite.Parameters including roasting temperature,dosage of ammonium sulfate,roasting time,and particle size of ore were investigated.Under the condition of roasting temperature of 400℃,roasting time of 5 h,ammonium sulfate dosage of 2.5 times of the theoretical value and ore particle size of 80−96μm,more than 98%leaching rate of aluminum was obtained.The phase transformation and mechanism during the roasting process were revealed by using X-ray diffraction,thermogravimetric analysis,differential thermal analysis,and scanning electron microscope methods.The diaspore and kaolinite phases in the silicon-rich diasporic bauxite could react with ammonium sulfate to form corresponding sulfates(NH_(4))_(3)Al(SO_(4))_(3) Al(SO_(4))_(2) and Al_(2)(SO_(4))_(3).The proposed technology could provide an effective method for the direct and separation of aluminum from silicon-rich diasporic bauxite.

Large scale preparation of phycobiliproteins from <i>Porphyra yezoensis</i>using co-precipitation with ammonium sulfate

The purpose of this study was to extract phyco-biliproteins (PBP) from Porphyra yezoensis using an optimized procedure and further establish a large scale process for protein production. According to our previous experiences on the extraction of PBP, salting out methods, e.g. ammonium sulfate precipitation, worked more efficiently than isoelectric precipitation, differential centrifugation or ultrafiltration. Thus, we chose ammonium sulfate to coprecipitate PBP in crude solution. After four times of precipitation followed by one time of high speed centrifugation, the maximum purity of crude phycoerythrin and phycocyanin reached 1.94 (A565/A280) and 0.85 (A615/A280), with a yield of 0.50% and 0.37%, respectively. A total of 0.94 mg phycoerythrin and 0.54 mg phycocyanin with purity of more than 3.2 were obtained from 1 g dried P. yezoensis after additional chromatography. We further scaled up the frozen dried P. yezoensis from 20 g to 400 g, with 1295 mg phycoerythrin and 593 mg phycocyanin obtained.

INVESTIGATION OF BEHAVIOR OF AMMONIUM SULFATE ON SURFACE OF IRON OXIDE Rong Sheng LI~*, Jing Feng CHEN, Hun YANG, Wu Yang ZHANG Dept. of Chemistry, Jilin University, Changchun 130023,

hhen ammonium sulfate-iron oxide is treated below 573 K, ammonium sulfate can spontaneously desperse on the surface of iron oxide. Simultaneously ammonium sulfate decomposes to some extent. During or after the dispersion, sulfate ion can interact with Fe atom on the surface of iron oxide to form a sort of surface sulfato complex of Fe and thus is transformed from the isolated into the bidentately bound form. Above 573 K the sulfato complex of Fe will gradually decompose with a further increase in temperature.

Physicochemical Study on the Interface Zone of Concrete Exposed to Different Sulfate Solutions

This paper reports the results of the visual observations and micro-analysis of concrete core samples after 6 and 12 months of their exposure to sodium, ammonium and magnesium sulfate solutions with the same concentration of sulfate ions. XRD, SEM and EDS were used for micro-analysis of the mi-crostructure and the composition of the interface zone in the samples. The results indicate that the deterioration of concrete by different sulfate solutions could proceed differently with regard to the mechanism and the mode of damage caused. The damage of concrete exposed to sodium sulfate solution is mainly caused by the gypsum crystals formed in the interface zone, which lead to expansion and cracking. In the case of concrete immersed in magnesium sulfate solutions, a layer of brucite (magnesium hydroxide) and gypsum was produced in the interface zone, which reduces the cohesiveness of the interface zone in concrete. For the concrete immersed in ammonium sulfate solutions, the conversation of mortar to some mush mass by ammonium ions and the formation of a large of gypsum occurred in the interface zone, consequently, serious softening of hydrated cement pastes and expansion and cracking of concrete are the characteristics of the attack by ammonium sulfate solutions. Also, it is considered that using drilled concrete core as samples to evaluate the sulfate resistance of concrete is a good and accelerated method.