Crystallization behaviors of bayerite from sodium chromate alkali solutions

In order to clean production of chromium compounds, it is a critical process to remove aluminates and utilize aluminum compounds from artificial chromate alkali solutions. The effects of Na2 Cr O4 on the neutralization curve, Al（OH）3 precipitation efficiency and induction period of bayerite were investigated. The results indicate that the neutralization curve of the artificial chromate alkali solutions shows three distinct regions and its induction period is longer than that of pure sodium aluminate solutions at the same aluminum concentration. And the decreased temperature and volume fraction of CO2 enhance the particle size of bayerite β-Al（OH）3. Bayerite composed of agglomerates of rods and cone frustums was obtained from alkali metal chromate solutions with 28.5% CO2（volume fraction） at temperatures ranging from 50 °C to 70 °C. Coarse bayerite with particle size（d50） from 24.2 μm to 29.3 μm extremely has few impurities, which is suitable for comprehensive utilization.

Variation of soda content in fine alumina trihydrate by seeded precipitation

High soda content in fine alumina trihydrate（ATH） limits its application and increases the soda consumption. The variation of soda content in the fine ATH by seeded precipitation was determined by detection of electric conductivity of solution, soda content in ATH, measurement of particle size distribution and microscopic analysis. The results show that high concentration of sodium aluminate solution, ground circulative seed, low temperature or fast initial precipitation rate increases the soda content in ATH. Soda mainly exists in lattice soda and less soda in desilication product （DSP） exists in the fine ATH precipitated from sodium aluminate solution with concentration of Al2O3 （ρAl2O3） more than 160 g/L and mass ratio of alumina to silica （μSiO2） of 400, and lattice soda decreases with increasing initial precipitation temperature, aging seed, and low precipitation rate and precipitation time. Results also imply that -＋ 4）Na Al（OH ion-pair influences lattice soda content in ATH on the basis of electric conductivity variation.

Enhancement on Synthesis of Boehmite Through a Precarbonizationassisted Hydrogen Peroxide Route in Highly Alkaline Sodium Aluminate Solutions

Hydrogen peroxide(H2O2)precipitation from sodium aluminate(SA)solution at close-ambient temperature is an efficient method to synthesize boehmite and its derived alumina with high surface area,but the precipitation yield of Al2O3 is usually below 50%in highly alkaline SA solutions.Here the synthesis of boehmite is enhanced through a precarbonization-assisted H2O2 route in highly alkaline SA solutions.It is found that the crystal structure of the precipitation product is evidently influenced by the precipitation conditions.As the precipitation temperature increases from 273 to 325 K,a small amount of gibbsite by-product is formed.As the aging temperature increases from 301 to 333 K,the crystallinity of boehmite decreases and part of the boehmite dissolves due to an increase in the pH value.Based on the above results,a precarbonization-assisted H2O2 route is proposed to obtain pure boehmite with more complete recovery of Al2O3 from highly alkaline SA solutions.The route includes a controllable precarbonization step of SA solutions with a molar ratio of Na2O to Al2O3 higher than 2:1,followed by the H2O2-precipitated step with a molar ratio of H2O2 to Al2O3 less than 7:1.Because of its facile operation conditions,no extraneous impurity,time saving and a possible recycle of the filtrate,the route has great potential to be an alternative method for preparation of boehmite and its derived alumina.

Wettability and surfactivity of sodium phosphate surfactants in strong alkali solutions

The wettability,surfactivity and the correlation between wettability and surfactivity of sodium diethylhexylphosphate,sodium diethylhexyl polyoxyethylene phosphate and their complex in NaOH solutions were studied.A complex alkali resistant phosphate surfactant with good permeability was prepared.The wettability of surfactants was investigated by measuring the immersion time,sinking time and capillary effects of nature cotton grey fabric in NaOH solutions.The surfactivity of the surfactants was characterized by measuring the surface tension.The effect of the complex on the surface appearance of cotton grey fabric was also investigated with a scanning electron microscope(SEM) .The results show that all the surfactants exhibit good wettability for cotton grey fabric in 0.5-5.0 mol/L of NaOH solutions,the complex system exhibits better wettability in 5.0-7.0 mol/L of NaOH solutions,in comparison with either corresponding single surfactant component employed,and wettability is well correlative with the surfactivities of the surfactant.SEM images indicate that the cotton grey fabric is well wetted by the alkaline surfactant solution and the quality of fabric is improved.

Investigation on the Key Factors and the Solution for pH Value Decrease in Carbon Filter in O3-BAC Process＊

An investigation was carried out to eliminate the decrease of effluent pH value in carbon filter in O3-biological activated carbon process. The influence factors were examined in a pilot test, and pH was adjusted in the pilot and waterworks. Results show that the carbon filter is an acid-base buffer system and the activated carbon is the key factor. Chemical functional groups on activated carbon surface present acid-base properties to buffer the water but decrease with time, so that effluent pH value decreases. The effects of ozone dosage, CO2 in the carbon filter, and the filter influent quality are negligible. A new method to adjust pH is developed: the activated carbon is first modified by soaking in sodium hydroxide solution to make its pH reach the desired value, and then the pH value of inflow is controlled to certain value by dosing lime in sand filter influent. The method is economical and effective.

Copper solvent extraction from alkaline cyanide solution with guanidine extractant LIX 7950

The use of the guanidine extractant LIX 7950 extracting copper and cyanide from alkaline cyanide solution was investigated.The extraction of copper and cyanide under different initial copper and extractant concentrations was examined and the stoichiometric extraction constant of Cu(CN)32- with LIX 7950 was calculated.Both the distribution coefficient and the stoichiometric extraction constant of Cu(CN)3 2-with LIX 7950 decrease when the temperature is varied from 25℃to 45℃, indicating the extraction process is exothermic.The calculated enthalpy change of the reaction(-HΘ)is about-190 kJ/mol.The copper extraction isotherms under different molar ratios of cyanide to copper are established.The preferential extraction of Cu(CN)32- over Cu(CN)4 3-and CN -has been confirmed and a high cyanide-to-copper molar ratio tends to suppress copper loading. The loaded copper and cyanide can be stripped efficiently by the moderately strong NaOH solutions(0.5-1.0 mol/L)and the presence of NaCN in the stripping solution facilitates copper stripping.

腐植酸的分析

【正】 4.1 原料煤中腐植酸的测定 本方法适用于泥炭、褐煤和风化煤中腐植酸含量的测定。 4.1.1 重量法 4.1.1.1 总腐植酸的测定 4.1.1.1.1 腐植酸总量(黄+棕黑HA)的测定 4.1.1.1.1.1