酸性光亮镀铜溶液的维护

简述酸性光亮镀铜的镀液配方和工作条件。各成份的作用及其对镀层质量的影响,并根据实际生产经验,介绍镀液的维护方法和镀液成份及工作条件的控制范围.

Continuous changes in electrical conductivity of sodium aluminate solution in seeded precipitation

The mechanism of seeded precipitation of sodium aluminate solution was studied by measuring the seeded-precipitation rate and electrical conductivity online, as well as calculating the activity and fraction of ion pair. The results show that the electrical conductivity of sodium aluminate slurry linearly decreases with increasing aluminum hydroxide addition. Moreover, both the electrical conductivity of slurry and the difference in electrical conductivity between sodium aluminate solution and slurry remarkably decline in the first 60 min before gradually increasing in the preliminary 10 h and finally reaching almost the same level after 10 h. In low Na2 O concentration solution the activities of Na OH and Na Al（OH）4 in seeded precipitation are high, which can enlarge the difference in conductivity between slurry and solution. Additionally, more ion pairs exist in solution in preliminary seeded precipitation, and the adsorption of Na＋Al（OH）4- on seed surface is likely to break the equilibrium of ion pair formation and to decrease the difference in conductivity in preliminary seeded precipitation.

Electrodeposition behavior and characteristics of Ni-carbon nanotube composite coatings

Ni-CNT (carbon nanotube) composite coatings were processed by electrodeposition and their hardness and corrosion characteristics were investigated with variations of CNT concentration in an electrolyte solution and electrodeposition current density. With increasing the CNT concentration in the electrodeposition bath and the current density, more CNTs are incorporated into Ni matrix. Hardness values of the Ni-CNT coatings are irrelevant to the CNT concentration in the solution, the current density, and current mode, implying poor adhesion of CNTs to Ni matrix. With increasing the CNT content in the coating, the corrosion resistance of the Ni-CNT composite coating becomes inferior due to the porous microstructure.

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.

Prediction of Activity Coefficients for Mixed Aqueous Electrolyte Solutions from the Data of Their Binary Solutions

The simple equation relating the activity coefficient of each solute in mixed electrolyte solution to its value in binary solutions under isopiestic equilibrium was tested by comparison with the experimental data for the 18 electrolyte solutions consisting of 1：1, 1：2, and 1：3 electrolytes. The isopiestic measurements were made on the quaternary system BaCl2-NH4Br-NaI-H2O and its ternary subsystems NaI-NH4Br-H2O, NaI-BaCl2-H2O, and NH4Br-BaCl2-H2O at 298.15K. The results were used to test the applicability of the Zdanovskii＇s rule to the mixed electrolyte solutions which contain no common ions, and the agreement is excellent. The activity coefficients of the solutes in the above quaternary and ternary systems calculated from the above-mentioned simple equation are in good agreement with the Pitzer＇s equation.

Characterization of polysulfone hollow-fiber ultrafiltration membrane and its cleaning efficiency by streaming potential and flux method

Polysulfone(PS)hollow-fiber ultrafiltration membrane was characterized combined with flux and streaming potential in single electrolyte solutions.The effects of trans-membrane pressure,electrolyte concentration,ion valence and pH value of electrolyte solution on the streaming potential(SP)of the membrane were investigated.The zeta potential and surface charge density of the membrane were calculated on the basis of Helmholtz-Smoluchowski equation and Gouy-Chapmann theory.The results indicate that the valence and concentration of cation have a greater influence on the SP and surface charge density of PS membrane than those of anion,and the pH value of electrolyte solution has great effects on the SP and zeta potential of the membrane surface. Both the absolute value of the streaming potential and water flux of the adsorbed membrane decrease,compared with those of the clean membrane.The streaming potential and flux of the cleaned membrane can be completely recovered by cleaning with the mass fraction of 0.8%EDTA at pH=10.

Preparation and Characterization of High Purity Enriched 10B Boric Acid via Anti-Solvent Recrystallization

Self-made enriched IUB boric acid as raw material was purified by recrystallization. The effects of final crystallization temperature, crystallization time, stirring speed, crystallization frequency and other factors on the purity were investigated. The appropriate operating condition was that the final crystallization temperature and time were 5 ℃ and 10 h respectively under a low-speed stirring for crystallizing twice, which would make the purity and yield of boric acid reach 99.94% and 95.36%, respectively. Taking this as foundation, recrystallization process was optimized with acetone as anti-solvent, whose amount was the most important index. The boric acid solution was added into acetone and recrystallized under the same condition, and the purity and yield of boric acid would reach 99.98% and 99.61%, respectively. The product detected by XRD was confirmed as boric acid crystal. Main ion concentration in the product was detected by ICP, which basically met the national standard of high purity. Crystal morphology of boric acid was observed by SEM.

The Electrodeposition of Rhenium in Alkaline and Acidic Elektrolytes

The investigation of electrodeposition of rhenium in alkaline and acidic electrolytes was carried out, polarization curves were obtained by electrochemically and cyclically potentiodynamic methods. By the investigation of rhenium concentration, sulphuric acid, alkali, ammonium sulphate, temperature and acidity of solution, it was found that reaming velocity was an optimal regime and electrolyte composition for an obtaining of high quality rhenium deposits from an alkaline electrolyte and acidic electrolyte. It was defined that the process of electrodeposition of rhenium in alkaline electrolyte is accompanied by chemical polarization and the electrodeposition of rhenium in acidic electrolyte goes gradually with the formation of intermediate films of sediments,

Direct Observation of Transition Metal Dichalcogenides in Liquid with Scanning Tunneling Microscopy

We present atomic-resolution images of TiSe2,MoTe2 and TaS2 single crystals in liquid condition using our home-built scanning tunneling microscopy(STM).By facilely cleaving of single crystals in liquid,we were able to keep the fresh surface not oxidized within a few hours.Using the high-stable home-built STM,we have obtained atomic resolution images of TiSe2 accompanied with the single atom defects as well as the triangle defects in solution for the first time.Besides,the superstructure of MoTe2 and hexagonal chargedensity wave domain structure in nearly commensurate phase of TaS2 were also obtained at room temperature(295 K).Our results provide a more efficient method in investigating the lively surface of transition metal dichalcogenides.Besides,the high stable liquid-phase STM will support the further investigations in liquid-phase catalysis or electrochemistry.

Membrane Potentials Across Hybrid Charged Mosaic Membrane in Organic Solutions

Membrane potentials across hybrid charged mosaic membrane in organic solutions were measured. Equilibrium swelling degree （SD） and fixed charge density in both organic solutions and water were also determined. Ethylene glycol, ethanol, n-propanol and glycerol were used as organic solutes; meanwhile 0.001mol-dm^-3 aqueous KCl solution was utilized as a strong electrolyte to measure the electrical difference. Equilibrium swelling degree indicated that it could be affected by the density of organic solutes; while it enhanced with the increasing density of these solutes. The measurement of fixed charge density showed that the membrane had the maximal absolute value in water among these solvents whether for cationic or anionic groups; the difference of dielectric constant between the water and the organic solutes might be responsible for these change trends. It was confirmed that membrane potentials increased with both the increasing concentration of the organic solutions and the elevated pH values. These results demonstrated that the characteristics of the hybrid charged mosaic membrane could be highly impacted by the properties of the organic solutes. A theoretical modal for charged membranes in ternary ion systems of weak electrolyte can be used to explain the above-mentioned phenomena.

Conductivity of Oxalic Acid in Aqueous Solution at Low Concentration

Oxalic acid is a weak and unsymmetrical bi-basic acid. There exist dissociation and association equilibria among the species in aqueous solution. The molar conductivity of the solution is the sum of the ionic contributions.Based on this idea, a new prediction equation of ionic conductivity was proposed at low concentration. The molar conductivities of the solution and its relevant ions were calculated respectively. The results obtained were in good agreement with those from experiments and the Quint-Viallard equation.

Densities, conductivities, and viscosities of aqueous solutions of N-hexyl,methylpyrrolidinium bromide and N-butyl, methylpyrrolidinium bromide at different temperatures

The densities, conductivities, and viscosities were measured for ternary solutions of N-hexyl,methylpyrrolidinium bromide([PP1,6]Br)- N-butyl,methylpyrrolidinium bromide([PP1,4]Br)-H2 O and its binary subsystems [PP1,6]Br-H2 O and [PP1,4]Br-H2 O at(298.15, 303.15, 308.15, and 313.15) K, respectively. The results were used to test the predictability of the simple equations established for the prediction of density, conductivity,and viscosity of the mixed electrolyte solutions. The results show that the examined simple equations can offer good predictions for density, conductivity, and viscosity of the mixed ionic liquid solutions in terms of the corresponding properties of its binary subsystems of equal ionic strength.

Electrokinetic phenomena of poly(vinyl butyral) hollow fiber membranes in different electrolyte solutions

The streaming potential of poly（vinyl butyral） （PVB） hollow fiber membrane was studied in different electrolyte solutions （including NaCl, KCl, CaCl2 and MgCl2）, the effects of ionic strength, ion valence and pH value on the streaming potential （SP） of the membrane were investigated. The zeta potentials and surface charge densities of the membrane were estimated on the basis of Helmholtz-Smoluchowski equation and Gouy-Chapmann theory. The results show that the PVB membrane has a weak negative charge due to the specific adsorption of ions. Moreover, the streaming potential, the zeta potential and the surface charge density of the membrane depend strongly on the salt concentration and the type and valence of ions. The iso-electric point （IEP） of the PVB membrane is arotmd 3.0 in the monovalent media （NaC1 and KC1） and 3.5 in divalent electrolytes （CaCl2 and MgCl2）. A few retentions were obtained for PVB membrane in low concentration solutions. This result verifies that the negative charged membrane surface can reject inorganic solutes by means of electrostatic repulsion effect even though the size of membrane pores is much larger than the size of salts.

Study of the Influence of the Electrolysis Parameters on Mn-Zn, Mn-Cu and Mn-Cu-Zn Alloys Coatings from Electrolytes Containing Complexing Ligands

The process of obtaining of high quality Mn-Zn, Mn-Cu and Mn-Cu-Zn alloy coatings from complexing ligands--citrate, EDTA （ethylene diaminetetra acetic acid） and nitrilotriacetic acid solutions was studied. Factors affecting stability of solutions containing ligand or ligands and influence of electrolysis parameters： electrolyte composition, pH, cathodic current density on chemical composition of the obtained coatings, on their current efficiency, morphology and structure were investigated.

Ultrasound assisted electrocatalytic oxidation of 3-chlorophenol in aqueous solution

Ultrasound assisted electrocatalytic process was used for enhancing decomposition efficiency of organic compounds. In this paper, the effect of ultrasonic frequency, ultrasonic intensity and pH value on 3-chlorophenol decomposition were studied. It was found that 3-chlorophenol in aqueous solution can be markedly decomposed by ultrasound assisted electrocatalytic process. The rate of decomposition increased with the increase of frequency, and low frequency is proper in the ultrasound assisted electrocatalytic system. The removal of 3-chlorophenol increased visibly with the increase of ultrasonic intensity until the intensity of 1.56 W/cm2. Alkaline condition is beneficial to 3-chlorophenol decomposition, the rate at pH 9.08 was higher than pH 2.48 and 6.85. The major intermediate formed during 3-chlorophenol decomposition was 2-chloro-pbenzoquinone, which was readily decomposed by ultrasound assisted electrocatalytic process.

Corrosion behavior of AZ31 magnesium alloy in simulated acid rain solution

The corrosion mechanism of AZ31 magnesium alloy used as automobile components and the influence of the concentration of Cl- ion in simulated acid rain(SAR)were studied by electrochemical tests and SEM.The results show that pitting corrosion happens around the AlMn phases locating at the grain boundary.The corrosion of AZ31 magnesium alloy in SAR is controlled by the rate of anodic dissolution and hydrogen evolution,and the corrosion rate of AZ31 increases with increasing concentration of Cl- ion.However,the Cl- ion in SAR is not the main influencing factor inducing the pitting corrosion.

CO_2 solubility in aqueous solutions of N-methyldiethanolamine+piperazine by electrolyte NRTL model

Accurate modeling of the solubility behavior of CO_2 in the aqueous alkanolamine solutions is important to design and optimization of equipment and process. In this work, the thermodynamics of CO_2 in aqueous solution of N-methyldiethanolamine(MDEA) and piperazine(PZ) is studied by the electrolyte non-random two liquids(NRTL) model. The chemical equilibrium constants are calculated from the free Gibbs energy of formation, and the Henry's constants of CO_2 in MDEA and PZ are regressed to revise the value in the pure water. New experimental data from literatures are added to the regression process. Therefore, this model should provide a comprehensive thermodynamic representation for the quaternary system with broader ranges and more accurate predictions than previous work. Model results are compared to the experimental vapor-liquid equilibrium(VLE), speciation and heat of absorption data, which show that the model can predict the experimental data with reasonable accuracy.

Calculation of CO_2, CH_4 and H_2S Solubilities in Aqueous Electrolyte Solution at High Pressure and High Temperature

This paper reports an investigation into the characterisation of liquidaivapor electrolyte solutions at high pressure and high temperature. A procedure to enable calcuIations of methane, carbon dioxide and hydrogen sulphide solubilities in brines (0-6 m.) for temperature from 25 to 350℃ and for pressures from 1 to 1800 bar is presented. The model is based on Helgeson, Kirkham and Flowers modified equations of state (HKF) and on the semi-empirical interaction model introduced by Pitzer. HKF modified equations of state are used to calculate the reference fugacity of gas species, and the Pitzer ionic interaction model is used to calculate the activity coefficient of dissolved species (i.e. ionic or neutral).The efficiency of the combination of the two models is confirmed by several comparisons with data in the literature.

Scaling Theory of Polyelectrolyte Nanogels

The present paper develops the scaling theory of polyelectrolyte nanogels in dilute and semidilute solutions. The dependencies of the nanogel dimension on branching topology, charge fraction, subchain length, segment number, solution concentration are obtained. For a single polyeleetrolyte nanogel in salt free solution, the nanogel may be swelled by the Coulombie repulsion （the so-called polyelectrolyte regime） or the osmotic eounterion pressure （the so-called osmotic regime）. Characteristics and boundaries between different regimes of a single polyelectrolyte nanogel are summarized. In dilute solution, the nanogels in polyeleetrolyte regime will distribute orderly with the increase of concentration. While the nanogels in osmotic regime will always distribute randomly. Different concentration dependencies of the size of a nanogel in polyeleetrolyte regime and in osmotic regime are also explored.