铝酸钠溶液晶种分解制备超细氢氧化铝结晶机理初步研究

采用铝酸钠溶液加凝胶晶种分解工艺制备出粒度分布窄、颗粒均匀的超细氢氧化铝,主要研究了温度、添加剂、晶种添加量等对分解率和晶体颗粒形貌的影响,并对晶体生长机理进行了分析研究。

Relationship between Al(OH)_3 solubility and particle size in synthetic Bayer liquors

Surface tension of sodium aluminate solution and the contact angle between Al（OH）3 particles and aluminate solution were measured, then the dependence of Al（OH）3 solubility on its particle size was calculated and thus the variation of the critical nucleus sizes was determined based on the Ostwald ripening formula. The results show that the Al（OH）3 solubility in sodium aluminate solution decreases with the increment of particle size, and the critical nucleus sizes increase with the rise of alkali concentration, caustic ratio and precipitation temperature. The results also imply that the presence of small particles in seeded precipitation system is an important factor to limit the depth of precipitation.

Adsorption of sodium polyacrylate at interface of dicalcium silicate-sodium aluminate solution

The adsorption isotherm of sodium polyacrylate on dicalcium silicate（2CaO-SiO2） in sodium aluminate solution at 80 ℃ was studied.The type of surface adsorption of sodium polyacrylate is saturated adsorption,and the adsorption behavior belongs to L-type,according with the monolayer adsorption model of Langmuir equation.The surface coverage of sodium polyacrylate is 1.06 mol/μm2.The relation curve between the surface pressure and the molecular area of adsorption film was obtained by Gibbs formula.The variation of interfacial energy caused by adsorption as well as the relationship between the relation curve and the type of adsorption was discussed.

怎样合理使用磷酸二氢钾

农作物在生长成熟过程中离不开磷、钾元素。正确地使用磷酸二氢钾，可提高农作物产量２０％～３０％，是一种最适用的化肥之一，其使用方法如下：（１）浸种：将种子泡在１：３００倍磷酸二氢钾水溶液中，浸种溶液面略高于种子面，浸泡２０小时后晒干播种。（２）拌种：将种子用１：５０倍磷酸二氢钾水溶液拌匀播种，每亩种子用磷酸二氢钾１５０克，加水７５千克的溶液浸泡。（３）叶面喷施：用０．１％～０.２％磷酸二氢钾水溶液在作物拔节、喇叭，孕穗期进行叶面喷施。每亩磷酸二氢钾用量为５０～１００克，用水约５０～７０千克。喷施磷酸二氢钾是一种补充性施肥措施，特别是叶面喷施，对玉米。薯类、水稻等有比较明显的增产效果。

Use of New Water Soluble Surface Film－Forming Material to Reduce Ammonia Loss from Water Solution

A new water soluble surfaCe film-forming material was developed and its effect on reducing ammonia volatilization from an alkaline solution was investigated in laborstory. Results showed that the new film formed by the material was not only more effective in reducing ammonia loss than any other films tested but also much cheaper. The optimum amount of addition of the new film-forming material was about 10times the theoretical amount to form a monomolecular film. Under the experimental conditions, the new film could effectively depress the ammonia volatilization for at least 6 days. The cumulative ammonia loss rates for different films were fitted to a simple logistic equation, and some important parameters such as the cumulative loss, and the maximum and average volatilization rates were calculated. The effect of different films could be, therefore, compared quantitatively, indicating the new film was most effective in depressing ammonia volatilization.

Effect of Surface Treatment on Flow Boiling Heat Transfer Coefficient in CaSO_4 Containing Water

This paper reports the influence of heat transfer surface treatment on the formation of calcium sulphate de-posit during flow boiling heat transfer. The surface of several test heaters was treated by surface modification techniques, such as dynamic mixing magnetron sputtering [DLC (diamond-like carbon), DLC-F (diamond-like carbon-fluorine) and AC (amorphous carbon)] and polishing to reduce surface energy. The results showed that heat transfer surface with low surface energy experienced significant reduction of formation of CaSO4 deposit. (1) Magnetron sputtering stainless steel heat transfer surface with DLC, DLC-F and plasma arc sputtering with AC did not change the surface roughness, but they reduced surface energy and improved heat transfer coefficient, so hindered CaSO4 deposit formation significantly. The DLC-F surface performed better than the DLC surface. (2) Surface energy played an important pole in improving heat transfer coefficient. The less the surface energy the more significant the heat transfer coefficient improved with other ex-perimental conditions identical. (3) The polished surface improved the roughness of the heater, but owing to the high sur-face energy it was not better than the DLC-F surface for a long-term consideration on improving the heat transfer coeffi-cient.

An EXAFS investigation of the mechanism of competitive sorption between Co(Ⅱ) and Ni(Ⅱ) at γ-alumina/solution interface

Co(Ⅱ)and Ni(Ⅱ)are two common toxic heavy metals,and may simultaneously exist in contaminated water,soil,and sediment systems in Earth’s surface environment.Under this circumstance,competitive adsorption between the two metals may influence their migration,toxicity,and bioavailability.In this research,the competitive sorption of Co(Ⅱ)and Ni(Ⅱ)on γ-Al_2O_3was studied using both macroscopic sorption experiments and extended X-ray absorption fine structure(EXAFS)spectroscopy.Results suggest that Ni(Ⅱ)reduced the amount of Co(Ⅱ)sorption in a binary-solute system at pH 6.0.This is because both Co(Ⅱ)and Ni(Ⅱ)form inner-sphere surface complexes during sorption on γ-Al_2O_3and compete for the surface reactive sites.However,Co(Ⅱ)exhibited a negligible influence on sorption amount of Ni(Ⅱ)under the same conditions,which suggests Ni(Ⅱ)has a stronger affinity to alumina surface.At pH 7.5,Co(Ⅱ)and Ni(Ⅱ)sorption density were much higher than that at pH 6.0,but there no mutual competitive effect was observed.EXAFS analysis further revealed that formation of layered double-hydrated precipitates was the dominant sorption mechanism for both Co(Ⅱ)and Ni(Ⅱ)at pH 7.5.Because this type of sorption does not rely on surface reactive sites,there was no competition between Co(Ⅱ)and Ni(Ⅱ).This finding sheds light on risk assessment and remediation of Ni/Co pollution.

Effects of ion-ion correlations on surface charge inversion in mixture electrolyte solutions

As the structure of electrical double layer(EDL)is crucial for the transport properties of ions in micro/nanochannels,to demonstrate the effects of the ion-ion correlations on EDL structures in mixture electrolyte solutions,the interaction forces between two mica surfaces immersed in different volume fractions of LaCl3/KCl and LaCl3/MgCl2 mixture solutions with a total ionic strength of 10^-4 mol/L were measured using a surface forces apparatus(SFA).The results reveal that the surface charge of mica surfaces can be inversed at a critical concentration of La^3+ions in electrolyte solutions,due to the correlations between La^3+ions.The addition of monovalent has negligible effects on ion-ion correlations,while the charge inversion was slightly suppressed by introducing the divalent ions.The mechanism of charge inversion in mixture electrolyte solutions was analyzed based on the strongly correlated liquid(SCL)theory.These findings provide implications for understanding the effects of ion-ion correlations on EDL structures,surface charge properties,and ion transportation.

Orientation and Structure of Ionic Liquid Cation at Air/[bmim][BF4] Aqueous Solution Interface

The watermiscible room temperature ionic liquid 1butyl3methylimidazolium tetrafluorob orate （[bmim] [BF4]） is a model system for studying the interactions between ionic liquid and water molecules. In this work the orientational structure of the low concentrated aqueous solution of [bmim] [BF4] at the air/liquid interface was investigated by sum frequency gener ation vibrational spectroscopy. It has been found that at very low concentrations, the butyl chain exhibited a significant gauche defect, indicating a disordered conformation; and the cation ring oriented with a fairly small tilting angle at the surface. When the concentration increased, the cation ring tended to lie flat at the surface, and the gauche defects of the butyl chain decreased due to the intermolecular chainchain interactions and the consequent more ordered interfacial molecular arrangement. Additionally, the antisymmetric stretching mode in the PPP and SPS spectra exhibited a peak shift, showing that there exists more than one kind of orientation or chemical environment for the butyl CH3 group. These results may shed new light on understanding the surface behavior of watermiscible ionic liquids as well as the imidazolium based surfactants.

Properties of low-modulus sodium silicate solution in alkali system

The properties of low-modulus(m≤1)sodium silicate and pre-desilication solutions in alkali systems were studied by measuring their electrical conductivity,viscosity,and surface tension.The results show that the property of high concentration pre-desilication solution is similar to that of sodium silicate solution.The electrical conductivity of sodium silicate solution increases with increasing the temperature and silica concentration but decreases with increasing the modulus.Further,the viscosity of the solution increases with increasing the silica concentration and linearly decreases with increasing the temperature,whereas its surface tension gradually decreases with increasing silica concentration and temperature,indicating that the sodium silicate solution is an oligomer with strong surface activity.At room temperature,the electrical conductivity and surface tension of sodium silicate solution are higher than those of pre-desilication solution,whereas its viscosity is smaller than that of pre-desilication solution.A turning point exists at a silica concentration of 44.7 g/L.When the silica concentration is less than 44.7 g/L,the ionic structure of the solution is dominated by monomeric silicate ions.In contrast,when the silica concentration changes from 44.7 to 50 g/L,the migration number of silicate anions significantly decreases.

Adsorption isotherm and inhibition effect of a synthesized di-(m-Formylphenol)-1,2-cyclohexandiimine on corrosion of steel X52 in HCl solution

The potential of di-(m-Formylphenol)-1,2-cyclohexandiimine as an environmentally friendly corrosion inhibitor for steel was investigated in 1 mol/L HCl using potentiodynamic polarization, electrochemical impedance spectroscopy and chronoamperometry measurements. All electrochemical measurements suggest that this compound is an excellent corrosion inhibitor for mild steel and the inhibition efficiency increases with the increase in inhibitor concentration. The effect of temperature on the corrosion behavior of mild steel with the addition of the Schiff base was studied in the temperature range from 25 °C to 65 °C. It is found that the adsorption of this inhibitor follows the Langmuir adsorption isotherms. The value of activation energy and the thermodynamic parameters such as ΔHads, ΔSads, Kads and ΔGads were calculated by the corrosion currents at different temperatures using the adsorption isotherm. The morphology of mild steel surface in the absence and presence of inhibitor was examined by scanning electron microscopy(SEM) images.

Solution-processed perovskite solar cells

Perovskite solar cells(PSCs) have emerged as one of the most promising candidates for photovoltaic applications. Low-cost, low-temperature solution processes including coating and printing techniques makes PSCs promising for the greatly potential commercialization due to the scalability and compatibility with large-scale, roll-to-roll manufacturing processes. In this review, we focus on the solution deposition of charge transport layers and perovskite absorption layer in both mesoporous and planar structural PSC devices. Furthermore, the most recent design strategies via solution deposition are presented as well, which have been explored to enlarge the active area, enhance the crystallization and passivate the defects, leading to the performance improvement of PSC devices.

Fabrication of Super Hydrophobic Surfaces on Copper by Solution-immersion

Super hydrophobic copper wafer was prepared by means of solution immersion and surface self-assembly methods. Different immersion conditions were explored for the best hydrophobic surface. Scanning electron microscopy (SEM), X-ray diffraction (XRD), energy dispersive spectrometer (EDS) and water contact angle measurements were used to investigate the morphologies, microstructures, chemical compositions and hydrophobicity of the produced films on copper substrates, respectively. Results show that the super hydrophobic surface is composed of micro structure of Cu 7 S 4 . The films present a high water contact angle larger than 150°, a low sliding angle less than 3°, good abrasion resistance and storage stability. The molecular dynamics simulation confirms that N-dodecyl mercaptan molecules link up with Cu 7 S 4 admirably, compared with Cu, which contributes to the stable super hydrophobic surface.

Partition Equilibrium Between Charged Membrane and Single Electrolyte Aqueous Solution

Ionic partition equilibrium in charged membrane immersed in solution of single electrolyte with monovalence or multi-valence is systematically investigated and several expressions are established for determination of partition coefficients. On this basis, the effects of the ratio of membrane charge density to bulk electrolyte solution concentration, the charge sign and valence of electrolyte ions and the type of membrane on the partition equilibrium were analyzed and simulated within chosen parameters. It is revealed that ion partition is not related solely with the respective concentrations but also definitely with the concentration ratio of fixed group to bulk solution in addition to the charge sign and the valence. For a counterion, the partition coefficient increases with this ratio and the valence; while for a coion, the partition coefficient decreases with this ratio and the valence. The theoretical calculations were compared with the experimental data and a good agreement was observed.

Electro-osmotic chemical behavior of clayey soil under various boundary conditions

The use of electro-osmotic chemical is an effective method to improve the clayey soil foundation.Various boundary conditions can be adopted in this method.In this work,two electrode–clay contacts,three solution conditioners,and four anode solution supply times were used for clayey soil improvement.Based on the experimental data,electro-osmotic consolidation theory,and transport of ion theory,it is found that the electro-osmotic chemical effect of the separation of electrode–clay(E_S)is more beneficial for the transport of Ca^(2+),production of cementing material,and reduction of water content than that of electrode–clay(E_C)joining;through electrode–clay contact separation,the anode solution conditioner(NaPO3)6(E_SHMP)delayed the cementing reaction and then increased the transport of Ca^(2+)near the cathode,which increased the amount of cementing material and the electro-osmotic chemical effect;and when the anode conditioner(NaPO3)6 was used,two days of anode solution supply followed by three days cut off from the anode solution led to the highest undrained shear strength increase after the application of electro-osmotic chemical,which resolved the uneven electro-osmotic chemical effect in the E_SHMP.

Lead Removal from Aqueous Solutions Using Novel Gel Adsorbent Synthesized from Natural Condensed Tannin

Lead has caused serious environmental pollution due to its toxicity, accumulation in food chains and persistence in nature. In this paper, removal of lead from aqueous solutions is investigated using a novel gel adsorbent synthesized from natural condensed tannin. The novel adsorbent performs in aqueous solutions as a weak base with valid basic groups of 1.2mmol·g-1 tannin gel particles and therefore results in the elevation of pH value of aqueous solutions. Even when initial pH is 3.6, final pH at equilibrium can climb up to 6.5 that is above the pH value for Pb(OH)2 precipitation formation and then lead can be removed from wastewater by this so-called surface precipitation. The adsorption isotherm can be expressed by the Langmuir equation and the maximum capacity for adsorption of Pb is up to 92 mg·g-1 (based on dry adsorbent) when initial pH value is 3.6. Hence, the adsorbent does offer favorable properties in lead removal with respect to its high adsorption capacity at low initial pH value, which is advantageous to lead removal from acidic wastewater. A model is put forward to describe the individual adsorption phenomenon of the tannin gel adsorbent.

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.

Adsorption Kinetics of Decanoyl-N-methylglucamine at the Expanding Spherical Surface

A general expression of the dynamic surface adsorption [Г（t）] on the expanding spherical surface was derived by solving the corresponding diffusion equation under different initial and boundary conditions. Different from the result of the still spherical surface, two factors （smaller than 1） appeared in the equation for the short time adsorption. Using the derived results, the adsorption kinetics of aqueous decanoyl-N-methylglucamine （Mega-10） solution was studied. In the short time region （t→0）, a good agreement of experimental results with the theory was reached and the adsorption was controlled by diffusion.

Electrochemical Performance of Zn（002） and Zn（100） Single Crystals in 6.0mol·L^-1 KOH

In this article, the electrochemical performance of the electrodes of zinc polycrystal, Zn（002） and Zn（100） single crystals were studied by the Tafel line extrapolation of the potentio-dynamic polarization curves, the cyclic voltammetry and the charge/discharge experiment. The results shows that in 6.0 mol·L^-1 KOH solution the corrosion rate of Zn polycrystal, Zn（100） and Zn（002） single crystals decreases in turn; and the reversibility and the charge/discharge performance of Zn single crystal was superior to Zn polycrystal. The dendrite growth of the surface of Zn polycrvstal was easier than Zn single crystal during the stages of charge/discharge.