Effect of Hydrated Calcium Aluminate Cement on the Chloride Immobilization of Portland Cement Paste

To improve the efficiency and stability of chloride immobilization of portland cement paste,hydrated calcium aluminate cement(HCAC)prepared by wet grinding of CAC was added into portland cement paste as an additive.The immobilized chloride ratio(ICR)was evaluated,and the mechanism of chloride immobilization was researched by XRD,DTG,NMR,and MIP tests.The analysis results demonstrated that HCAC could improve the chloride immobilization capacity of portland cement paste.The mechanism was attributed to the following aspects:chemical binding capacity was enhanced via producing more Kuzel’s salt;physical adsorption capacity was reduced by decreasing the C-S-H gel;migration resistance was enhanced through refining the pore structure.

Chloride Corrosion of Reinforced Calcium Aluminate Cement Mortar

This paper describes a study on the corrosion behavior of steel reinforcement in CAC mortars via electrochemical methods including corrosion potential,electrochemical impedance,and linear polarization evaluation.Results indicate that there is a non-linear relationship between the corrosion degree of steel reinforcement in CAC mortar and the concentration of NaCl solution.The electrochemical parameters of specimens immersed in 3%NaCl solution suddenly drop at 40 days,earlier than 60 days of the reference.And the charge transfer resistivity of the specimen has decreased by 11 orders of magnitude at 40 days,showing an evident corrosion on steel reinforcement.However,it is interesting to notice that the corrosion is delayed by high external chloride concentration.The specimens immersed in 9%and 15%NaCl solutions remain in a relatively stable state within 120 days with slight pitting.The great corrosion protection of CAC concrete to embedded steel bars enables its wide application in marine.

Fluoride Ion Adsorption Effect and Adsorption Mechanism of Self-Supported Adsorbent Materials Based on Desulfurization Gypsum-Aluminate Cement

The adsorption method has the advantages of low cost,high efficiency,and environmental friendliness in treating fluorinated wastewater,and the adsorbent material is the key.This study combines the inherent anion-exchange adsorption properties of layered double hydroxides(LDHs).Self-supported porous adsorbent materials loaded with AFm and AFt were prepared from a composite cementitious system consisting of calcium aluminate cement(CAC)and flue gas desulfurization gypsum(FGDG)by chemical foaming technique.The mineral composition of the adsorbent material was characterized by X-ray diffraction(XRD)and Scanning electron microscopy(SEM).Through the static adsorption experiment,the adsorption effect of the mineral composition of the adsorbent on fluoride ions was deeply analyzed,and the adsorption mechanism was revealed.XRD and SEM showed that the main hydration phases of the composite cementitious system consisting of CAC and FGDG are AFm,AFt,AH_(3),and CaSO_(4)·2H_(2)O.FGDG accelerates the hydration process of CAC and inhibits the transformation of AFt to AFm.The AFt content increased,and the AFm content decreased or even disappeared as the amount of FGDG increased.Static adsorption experiment results showed that AFm and AFt in adsorbent materials could significantly enhance the adsorption of fluoride ions.The adsorption of F^(−)in aqueous solution by PAG tends more towards monolayer adsorption with a theoretical maximum capacity of 108.70 mg/g and is similar to the measured value of 112.77 mg/g.

Effect of Al Powder and Si Powder Additions on Structure and Properties of Unburned Magnesium Aluminate Spinel Refractories

Unburned magnesium aluminate spinel refractories were prepared using sintered magnesium aluminate spinel as the main raw material,phenolic resin as the binder,aluminum powder(2%,4%,and 6%by mass)and silicon powder(when Al powder addition is 4%,Si powder addition varies:1%and 2%,by mass)as additives.The effects of the Al powder and Si powder additions on the properties and microstructure of the refractories heat treated at different temperatures(1000,1400,and 1600℃for 3 h)were studied.The results show that the Al powder addition can greatly enhance the cold modulus of rupture of the samples fired at 1000 or 1400℃,and meanwhile AlN reinforcement phase forms in the matrix,which greatly improves the hot modulus of rupture of the samples at 1400℃;however,the heat treatment at 1600℃has little influence on the strength;the addition of Al powder and Si powder results in the formation of low melting point phases,greatly reducing the hot modulus of rupture.However,the low melting point phases promote sintering,which enhances the density and the cold modulus of rupture,and decreases the volume change during heating.The samples added with Al and Si all have higher cold modulus of rupture than those added with Al powder only.

Effect of ZrO_(2)Addition on Lanthanum Aluminate-based High Emissivity Coating Materials

In order to enhance the sintering resistance of lanthanum aluminate based high emissivity coatings,Ca^(2+)-Fe^(3+)doped LaAlO_(3)/ZrO_(2)specimens were prepared by solid state sintering using La_(2)O_(3),Al_(2)O_(3),CaCO_(3) and Fe_(2)O_(3) as raw materials,extra-adding fused Y_(2)O_(3)-stabilized ZrO_(2)(0,5%,10%,and 15%,by mass),ball milling,pre-calcining,pressing into shapes and sintering at 1600℃for 2 h.The effect of the ZrO_(2)addition on the properties of lanthanum aluminate based high emissivity coatings was explored.It is concluded that ZrO_(2)does not react with LaAlO_(3),which can inhibit the sintering of the specimens.With the increase of the ZrO_(2),addition,the linear shrinkage rate and the thermal conductivity decrease significantly,while the emissivity decreases,but the emissivity of all the specimens is all higher than 0.9.The optimal addition of ZrO_(2),is 10%.

Pre-desilication and digestion of gibbsitic bauxite with lime in sodium aluminate liquor

The effect of lime on the pre-desilication and digestion of gibbsitic bauxite in synthetic sodium aluminate liquor at different tem- peratures was investigated. The bauxite is comprised of gibbsite, aluminogoethite, hematite, kaolin, quartz, and minor boehmite. Lime in- creases the desilication efficiency of the bauxite during the pre-desilication process by promoting the conversion of sodalite and cancrinite to hydrogamet. Desilication reactions during the digestion process promoted by lime result in the loss of A1203 entering the red mud, but the amount of aluminogoethite-to-hematite conversion promoted by lime leads to the increase of aluminogoethific A1203 entering the digested liquor. The alumina digestion rate at 245~C is higher than that at 145 C due to the more pronounced conversion of aluminogoethite to hema- tite. The soda consumption during the digestion process decreases due to lime addition, especially at higher temperatures.

INFLUENCE OF PREPARATIVE HISTORY ON STRUCTURE AND PROPERTIES OF SODIUM ALUMINATE SOLUTIONS

It has been found that samples of sodium aluminate solutions with the same composition but different preparative history may have difTerent structure and physico-chemical properties.The structure of sodium-bearing aluminate solutions change very slowly during the storage after preparation.Sodium aluminate solutions contain several ammunium-bearing anisons such as Al(OH)^(-)_(4),Al(OH)^(3-)_(6)and[(HO)_(3)Al-O-Al(OH)_(3)]^(2-),etc.These anions can convert to each other but the reactions are very slow owing to the formation or breakage of covalent Al-O bond.Hence the ratio between these anions approaches equilibrium very slowly after the preparation,and the structure or properties of these solution samples before equilibrium is reached depend on their preparative histosive.

Influence of the Preparative History on Physico-chemical Properties of Sodium Aluminate Solutions

1.IntroductionSodium aluminate solutions are veryimportant intermediate products in alumin-ium metallurgy.The physico-chemicalproperties of sodium aluminate solutions areconcerned by metallurgists and engineersdealing with alumina production[1].Thedata of viscosity,electroconductivity,UV

Investigations on Valence-Change Behaviors of Europium Ions in Eu-Doped Aluminate and Silicate Phosphors

Compounds of Sr3Al2O6 ： Eu, SrgAl14O25 ： Eu, and BaZnSiO4 ： Eu were synthesized by high-temperature solid state reactions. The doping Eu^3 ＋ ions were partially reduced to Eu^2＋ in Sr4Al14O25：Eu and BaZnSiOg：Eu prepared in an oxidizing atmosphere, N^2 ＋ O2. However, such an abnormal reduction process could not be performed in Sr3Al2O6：Eu, which was also prepared in an atmosphere of N^2 ＋ O2. Moreover, even though Sr3A1EO6：Eu was synthesized in a reducing condition CO, only part of the Eu^3 ＋ ions was reduced to Eu^2 ＋ . The existence of trivalent and divalent europium ions was confirmed by photoluminescent spectra. The different valence-change behaviors of europium ions in the hosts were attributed to the difference in host crystal structures. The higher the crystal structure stiffness, the easier the reduction process from Eu^3 ＋ to Eu^2 ＋ .

Effect of Magnesium on the C-S-H Nanostructure Evolution and Aluminate Phases Transition in Cement-Slag Blend

The microstructural study was conducted on cement and cement-slag pastes immersed in different concentrations of Mg（NO3）2 solutions utilizing ^29Si, ^27Al NMR spectroscopy and XRD techniques. The results show that the hydration of both the cement and cement-slag pastes is delayed when the pastes are cured in Mg（NO3）2 solutions as compared to the pastes cured in water. Moreover, Mg^2＋ ions also exhibit an decalcifying and dealuminizing effect on the C-A-S-H in cement and cement-slag pastes, and thereby decrease Ca/Si and Al[4]/Si ratios of the C-A-S-H. The dealuminization of C-A-S-H is mitigated for cement-slag paste as compared to pure cement paste. The depolymerized calcium and aluminum ions from C-A-S-H gel mainly enter the pore solution to maintain the pH value and form Al^[6] in TAH, respectively. On the other hand, Mg^2＋ ions exert an impact on the intra-transition between Al^[6] species, from AFm and hydrogarnet to hydrotalcite-like phase. NO3^-ions are interstratified in the layered Mg-Al structure and formed nitrated hydrotalcite-like phase（Mg1-xAlx（OH）2（NO3）x·nH2O）. Results from both ^27Al NMR and XRD data show that ettringite seems not to react with Mg^2＋ ions.

Roles of crystal defects in the persistent luminescence of Eu^(2+), Dy^(3+) co-doped strontium aluminate based phosphors

The roles of different point defects in persistent luminescence of SrAl2O4：Eu,Dy phosphors were investigated. The research results showed that Dyer plays an important role in the persistent luminescence of SrA1EO4：Eu, Dy phosphors. It can serve as the electron trap of suitable depth for persistent luminescence. V~ does not serve as the electron trap of suitable depth, but its existence can increase the depth of electron traps. There is interaction between the Dy^3＋（ DySr ） and the Eu^2＋（Eu^x Sr ）, and only if the distance between the Dy^3＋（DySr） and the Eu^2＋ （Eu^x Sr） is close enough, the Dyer can work as an effective electron trap. The point defect of V＂ Sr can be hole trap, but the change of its density in crystal matrix does not arouse the obvious change of persistent luminescence.

Precipitation of spherical boehmite from concentrated sodium aluminate solution by adding gibbsite as seed

The precipitation of spherical boehmite was studied by surface energy calculations, measurements of precipitation ratios, Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. The surface energy calculation results show that the(001) and(112) planes of gibbsite surfaces are remarkably stable because of their low surface energies. In addition, the(010) plane of boehmite grows preferentially during precipitation because of its low surface energy. Thus, we propose a method to precipitate spherical boehmite from a supersaturated sodium aluminate solution by adding gibbsite as seed in a heterogeneous system. In this method, gibbsite acts as the preliminary seed and saturation modifier. The results show that the fine boehmite first nucleates on the(001) and(112) planes of gibbsite and then grows vertically on the(001) and(112) basal planes of gibbsite via self-assembly, thereby forming spherical boehmite. Simultaneously, gibbsite is dissolved into the aluminate solution to maintain the saturation for the precipitation of boehmite. The precipitation ratio fluctuates(forming an M-shaped curve) because of gibbsite dissolution and boehmite precipitation. The mechanism of boehmite precipitation was further discussed on the basis of the differences in surface energy and solubility between gibbsite and boehmite. This study provides an environmentally friendly and economical method to prepare specific boehmite in a heterogeneous system.

Copper doped nickel aluminate: Synthesis, characterisation, optical and colour properties

Novel environment friendly inorganic nano green pigments,Ni1-xCuxAl2O4(x=0,0.02,0.04,0.06,0.08,0.1)were successfully synthesised by simple,cost effective sol–gel method using citric acid as a gelling agent.Synthesised nano pigments were characterised by powder XRD,FT-IR,UV-DRS,SEM–EDX and TEM.Distribution of elements such as Ni,Cu,Al and O for the pigment Ni0.98Cu0.02Al2O4 was authenticated by elemental mapping analysis.The colour parameters were studied using CIE-LAB parameters.It is evident from the DRS measurement that the band gap energy of Ni Al2O4(3.11 eV)has been massively diminished to 2.63 eV when x=0.02,unexpectedly changed the colour of the pigment from cyan to green.Whilst x=0.1 the pigment colour has turned into grey and the corresponding band gap condensed into 2.17 eV.Effect of mineralisers like NaF,CaF2,NH4H2PO4 and Li2CO3 on the colour of Ni0.98Cu0.02Al2O4 was investigated.

Mineral transition and formation mechanism of calcium aluminate compounds in CaO-Al2O3-Na2O system during high-temperature sintering

The mineral transition and formation mechanism of calcium aluminate compounds in CaO-Al2O3-Na2O system during the hightemperature sintering process were systematically investigated using DSC-TG,XRD,SEM-EDS,FTIR,and Raman spectra,and the crystal structure of Na4Ca3(AlO2)10 was also simulated by Material Studio software.The results indicated that the minerals formed during the sintering process included Na4Ca3(AlO2)10,CaO·Al2O3,and 12 CaO·7 Al2O3,and the content of Na4Ca3(AlO2)10 could reach 92 wt%when sintered at 1200°C for 30 min.The main formation stage of Na4Ca3(AlO2)10 occurred at temperatures from 970 to 1100°C,and the content could reach82 wt%when the reaction temperature increased to 1100°C.The crystal system of Na4Ca3(AlO2)10 was tetragonal,and the cells preferred to grow along crystal planes(110)and(210).The formation of Na4Ca3(AlO2)10 was an exothermic reaction that followed a secondary reaction model,and its activation energy was 223.97 kJ/mol.

Effects of SrO/Al_2O_3 Molar Ratio on the Luminescent Characteristics of Rare-Earth Strontium Aluminate Phosphors

The study on the effects of SrO/Al 2O 3 molar ratio on the crystalline phases and photoluminescence characteristics of strontium aluminate phosphors co-activated with Eu 2+ and Dy 3+ were conducted by X-ray powder diffractometry, fluorescence spectrometer and photometer. The strontium aluminate luminescent materials with different SrO/Al 2O 3 molar ratio emit the visible lights with different color tone after removal of excitation. The peak wavelengths of the emission spectra drift in the direction of short wave, the quantity of Sr 4Al 14O 25 crystalline phase increases and the afterglow time lengthens with the SrO/Al 2O 3 reduction. The results show that when the SrO/Al 2O 3 molar ratio is near 1, the photoluminescence materials have high luminescent intensity, and when it is near 0.75, they have long afterglow time. However, when SrO/Al 2O 3 molar ratio is more than 1, the luminescent materials appear strong alkaline in water solution; when SrO/Al 2O 3 molar ratio is much less than 0.75, the samples need a higher temperature to be sintered.

RAMAN SPECTRA OF SODIUM ALUMINATE SOLUTIONS WITH HIGH-CAUSTIC RATIO AND HIGH CONCENTRATION

The constitution of high-caustic ratio and highly concentrated sodium aluminate solutions has been investigated by Raman spectra method.By comparison with the Raman spectra of crystalline solids of Ca_3[Al(OH)_6]_2 and Ba_2[Al_2(OH)_(10)],it can be concluded that AI(OH)_6^(3-)ion and perhaps its polymers may be formed in these solutions.

Recovery of iron and calcium aluminate slag from high-ferrous bauxite by high-temperature reduction and smelting process

A high-temperature reduction and smelting process was used to recover iron and calcium aluminate slag from high-ferrous bauxite. The effects of w（CaO）/w（SiO_2） ratio, anthracite ratio, and reduction temperature and time on the recovery and size of iron nuggets and on the Al_2O_3 grade of the calcium aluminate slag were investigated through thermodynamic calculations and experiments. The optimized process conditions were the bauxite/anthracite/slaked lime weight ratio of 100：16.17：59.37, reduction temperature of 1450°C and reduction time of 20 min. Under these conditions, high-quality iron nuggets and calcium aluminate slag were obtained. The largest size and the highest recovery rate of iron nuggets were 11.42 mm and 92.79wt%, respectively. The calcium aluminate slag mainly comprised Ca_2 SiO_4 and Ca_（12）Al_（14）O_（33）, with small amounts of Fe Al_2O_4, CaAl_2O_4, and Ca_2Al_2SiO_7.

Experimental Verification on Conversion Mechanism of Calcium Aluminate Cement Hydrates

Calcium aluminate cement(CAC)is a commonly used binder for refractory castables.There has been a long-running debate on the transformation mechanisms of calcium aluminate cement hydrates through solid-state reaction or solutionprecipitation.In order to demonstrate the conversion mechanism of CaO Al2O310H2O(CAH10)to 3CaO Al2O36H2O(C3AH6)and Al2O33H2O(AH3),the CAC pastes cured at 10℃to produce CAH10 was further cured at 60℃with and without free water.The hydration of the pastes was halted by freezing-drying,and the phases and microstructure of hydrates were investigated by XRD and SEM,respectively.The results indicate that CAH10 converts into C3AH6 and AH3 in water presence at 60℃,but does not transform into C3AH6 and AH3 without water,demonstrating that conversion of CAH10 into C3AH6 and AH3 does not happen through solid-state reaction,but takes place through preceding dissolution of CAH10 and subsequent precipitation of AH3 and C3AH6 from the solution.

Effect of Curing Temperature on Intermediate Temperature Properties of Calcium Aluminate Cement Bonded Corundum Castables

In order to study the effect of the curing temperature on the intermediate temperature properties of calcium aluminate cement bonded corundum castables,the prepared castables were cured at 5,10,25,40 and 50℃,respectively,dried at 110℃ for 24 h and heat treated at 800 and 1100 ℃,respectively.Then the apparent porosity,the cold modulus of rupture and the cold crushing strength were measured.The phase composition of castable matrix specimens treated under the same conditions and the influence of the curing temperature on the intermediate temperature strength of the castables were also analyzed.The results show that with the increase of the curing temperature,the hydration degree of calcium aluminate cement increases,which promotes the uniform distribution of hydration products with AI203 after decomposition,thus enhancing the intermediate temperature strength of castables.

Preparation of Incompact Strontium Aluminate Phosphors

The incompact long afterglow pigment SrAl2O4: Eu, Dy was synthesized by ceramics technology.The agglomerated starting raw material had little effect on the synthesis of SrA12O4 matrix through solid-state reaction method,but the shrinkage and densification was retarded greatly by the agglomerated powder by the formation of large and extensive pore network.The sintering mechanism is surface diffusion ( without flux B2O3 ) and grain boundary diffusion (with B2O3 as flux)respectively, and the as-prepared long afterglow pigment glows in the dark for over 4000 min.