酸碱溶液进入除盐水系统的风险因素识别及削减措施

通过对酸、碱溶液进入除盐水系统的风险因素识别及削减措施,科学准确的判定酸、碱溶液进入除盐水系统原因,采取及时有效的措施,减少危害的进一步扩大,制定相应的削减措施,从而实现除盐水装置长期稳定运行的目的。

化学价值在教学过程中的渗透研究——以酸、碱、盐在水溶液中的电离为例

以“酸、碱、盐在水溶液中的电离”的课堂教学设计为例,通过分析化学价值形成过程,阐述化学价值在实际教学过程中的渗透过程,以期为一线教学提供参考和借鉴。

有关溶液pH的计算

结合化学教学实践,探讨了酸、碱、盐、缓冲溶液及溶液稀释时pH的计算方法及规律。

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.

Effects of additives on zinc electrodeposition from alkaline zincate solution

The effects of additives on the surface and cross-sectional morphologies of zinc deposits on iron substrate from alkalinezincate solution were characterized by scanning electron microscope(SEM).The cathodic reaction mechanisms under variousconcentrations of additives were investigated using cyclic voltammetry(CV)and electrochemical impedance spectroscopy(EIS)techniques.It is found that with increasing the additive A content in the bath solution,the nucleation overpotential(NOP)value isobviously increased and the inhibition effect is strengthened.This may be mainly due to the adsorption of additive A on the cathodicelectrode surface,which can cover the active sites and block the discharge reduction.The results of EIS analysis indicate that therate-determining step of zinc electrodeposition process is changed from mixed control step into electrochemical reduction step in thepresence of additive A.However,any quantity of additive B has little effect on the NOP value and the inhibition effect is not obvious.Furthermore,addition of additive A and additive B at the same time displays the strongest inhibition effect and shows a strongsynergism because of their co-adsorption on the cathodic electrode surface.

Preparation of spherical cobalt carbonate from cobalt sulfate solution

A precursor of cobaltous dihydroxycarbonate was firstly prepared by precipitation reaction of cobalt sulfate solution and ammonium carbonate solution,and then a hydrothermal process for the precursor was conducted to obtain the spherical cobalt carbonate with low sulfur content.The experimental results show that the feeding method,final p H value of the precipitation reaction slurry and the concentration of the cobalt sulfate solution have obvious effects on the sulfur content,morphology and particle size distribution of the precursor.The sulfur content of the precursor is 0.0115 wt.%under the optimized conditions.The hydrothermal treatment with temperatures of 125-150℃can transform the precursor of cobaltous dihydroxycarbonate into spherical cobalt carbonate and decrease the sulfur content to 0.0030 wt.%in the obtained product.

石膏岩溶蚀与强度特性试验研究

石膏岩在工程中使用广泛,其具有特殊的物理化学性质,常引发工程问题,因此研究石膏岩的溶蚀特性以及溶蚀前后强度、塑性、脆性等性质变化显得尤为重要。通过室内溶蚀试验分析其溶蚀机理,利用电镜扫描观察其微观结构,分析强度劣化机理,并通过单轴压缩试验,研究石膏岩在不同溶液条件下的软化性质。结果表明,不同溶液对石膏岩的影响不同。以石膏岩浸泡在纯水中为参照,NaCl溶液促进石膏岩的溶蚀量,使试样的强度降低,为纯水溶蚀后试样强度的40%,塑性变强,脆性减弱;冰醋酸溶液减少石膏岩的溶蚀量,强度少许增加,塑性变弱,脆性变强;氢氧化钠溶液可与石膏岩发生反应生成氢氧化钙,因此在前期可促进石膏岩的溶蚀,后期生成较多的氢氧化钙络合物附着在岩样表面阻止石膏岩继续溶蚀并使其强度变大、塑性变强。微观电镜图片显示,不同溶液对石膏岩的溶蚀程度以氯化钠溶液最为严重,其次分别为纯水、冰醋酸溶液、氢氧化钠溶液。单轴压缩试验时声发射活动发生次数与溶蚀量相一致。

Kinetics of Zn cathodic deposition in alkaline zincate solution

Kinetic parameters of the electrode reactions were measured by investigating steady-state current-potential behaviors. The Tafel slopes of cathodic and anodic processes are -0.113 8 V and -0.041 18 V, the anodic and cathodic apparent transfer coefficients are 0.519 3 and 1.435 2, respectively, and the stoichiometric number of rate-deterrnining step is 1. The theoretical kinetics equation of electrode reaction was deduced, from which the dynamic parameters can be calculated as follows： the cathodic and anodic Tafel slopes are -0.118 V and -0.039 4 V, respectively, consisting with the experimental values, Finally, the correctness of the mechanism was further demonstrated using apparent transfer coefficient according to the electrochemical dynamic equation of multi-electron reaction.

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.

Leaching kinetics of low-grade copper ore with high-alkality gangues in ammonia-ammonium sulphate solution

The leaching kinetics of low-grade copper ore with high-alkality gangues was studied in ammonia-ammonium sulphate solution.The main parameters,such as ammonia and ammonium sulphate concentrations,particle size,solid-to-liquid ratio and reaction temperature,were chosen in the experiments.The results show that the increase of temperature,concentrations of ammonia and ammonium sulphate is propitious to the leaching rate of copper ore.The leaching rate increases with the decrease of particle size and solid-to-liquid ratio.The leaching rate is controlled by the diffusion through the ash layer and the activation energy is determined to be 25.54 kJ/mol.A semi-empirical equation was proposed to describe the leaching kinetics.

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.

A Mechanism Study of a Novel Acid-Activatable Michael-Type Fluorescent Probe for Thiols

A Michael addition is usually taken as a base-catalysed reaction. However, our synthesized 2-（quinolin-2-ylmethylene） malonic acid （QMA） as a Michael-type thiol fluorescent probe is acid-active in its sensing reaction. In this work, based on theoretic calculation and experimental study on 7-hydroxy-2-（quinolin-2-ylmethylene） malonic acid, we demonstrated that QMA as a Michael acceptor is acid-activatable, i.e., it works only in solutions at pH〈7, and the lower the pH of solutions is, the higher reactivity QMA has. In alkaline solution, the malonate QMA[-2H＋]2- cannot react with both RSand RSH. In contrast, 2-（quinolin-2- ylmethylene） malonic ester （QME）, the ester of QMA, reveal a contrary pH effect on its sensing reaction, that is, it can sense thiols in alkaline solutions but not in acidic solutions, like a normal base-catalysed Michael addition. The values of activation enthalpies from theoretic calculation support the above sensing behavior of two probes under different pH conditions. In acidic solutions, the protonated QMA is more highly reactive towards electrophilic attack over its other ionized states in neutral and alkaline solutions, and so can react with lowly reactive RSH. In contrast, there is a big energy barrier in the interaction of QME with RSH （acidic solutions）, and the reaction of QME with the highly reactive nucleophile RS- is a low activation energy process （in alkaline solutions）. Theoretic calculation reveals that the sensing reaction of QMA undergoes a 1,4-addition process with neutral thiols （RSH）, and a 1,2-addition pathway for the sensing reaction of QME with RS-. Therefore, the sensing reaction of QMA is an acid-catalysed Michael addition via a 1,4-addition, and a normal base-catalysed Michael addition via a 1,2-addition.

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.

Comparison of dissolution profile characteristics of 11 berberine hydrochloride tablet brands in different dissolution media

Berberine hydrochloride is commonly used to treat bacterial dysentery,gastroenteritis and other diseases.Many manufacturers are available on the market today,while the production process and formulation are quite different,which may directly affect the therapeutic effect of the drug.To this end,11 different production producers of berberine hydrochloride tablets were collected according to the pharmacopeia berberine hydrochloride dissolution method(basket method).In addition the dissolution process was carried out in four elution media with different pH,and the difference was similar(f2).Factors were calculated to evaluate in vitro dissolution requirements,and in vitro dissolution of different manufacturers of berberine hydrochloride tablets was determined by high performance liquid chromatography(HPLC).The method was verified by linearity,precision,stability and robustness.Based on the f2 value,there was a significant difference in the dissolution behavior of the formulations of most berberine hydrochloride tablet brands.This research provided the basis for further in-depth research in the later period.Although the drug specifications(0.1 g)were the same,the dissolution curve was different.This phenomenon may be attributed to the fact that the excipients and crystal form of the tablets affected the release and dissolution of the tablets in vitro.