Properties of Geopolymers Made from Fired Clay Bricks Wastes and Rice Husk Ash (RHA)-Sodium Hydroxide (NaOH) Activator

High cost has been pointed among factors that limit the promotion of geopolymers. To contribute to the reduction of the use of costly industrial sodium silicate in activators for geopolymers, a gel obtained with RHA and concentrated sodium hydroxide was used in the present study to develop an alkaline activator with 8 M NaOH and to produce geopolymers with crushed fired clay bricks wastes (FCBW). Characteristics of the gel were compared to that of commercial sodium silicate which was also mixed with 8 M NaOH in the ratio 1:1 to produce geopolymers. Chemical and mineralogical analyses were done on raw materials. Fourier Transformed Infrared Spectroscopy (FTIR) was done on the gel, commercial sodium silicate and products. Biaxial four point flexural strength, bulk density, water absorption and scanning electron microscopy (SEM) tests were also done on products. Results showed that RHA-NaOH alkaline activator has good potential in consolidating FCBW powder through geopolymerization process which gave products that had characteristics not far from that when the commercial sodium silicate was used. The gel obtained by mixing RHA and NaOH can contribute to the reduction of the use of costly commercial sodium silicate in the production process of geopolymers. However, appropriate filtration process is needed for the RHA-NaOH gel to reduce its impurities as undissolved entities, which will consequently contribute to improve the flexural strength, the density and the microstructure of its products which were low compared to when commercial sodium silicate was used.

Measurements of zinc oxide solubility in sodium hydroxide solution from 25 to 100 °C

The solubility of zinc oxide in sodium hydroxide solution was measured in a closed polytetrafluoroethylene vessel from 25 to 100 ℃. The ZnO solubility was determined by employing the method of isothermal solution saturation. The results show that only ZnO solid exists in the equilibrium state in the low concentration alkali regions, and the solubility of zinc oxide is almost invariable with temperature. With the increase of alkali concentration, equilibrium solid turns from ZnO to NaZn（OH）3 suddenly, this mutation is called invariant point. The alkali concentration of the invariant points increases with increasing temperature, but the solubility of NaZn（OH）3 decreases with increasing alkali concentration at the same temperature. At the same Na2O concentration, the higher the temperature is, the higher the solubility of NaZn（OH）3 is.

Leaching kinetics of scheelite concentrate with sodium hydroxide in the presence of phosphate

The reaction kinetics for the leaching of low-grade scheelite concentrate was investigated in an autoclave with sodium hydroxide in the presence of phosphate. The effects of stirring speed (300-600 r/min), reaction temperature (353-383 K), sodium hydroxide concentration (1.69-6.76 mol/L) and phosphate concentration (0.68-1.69 mol/L) on the WO3 dissolution ratio were studied. The results showed that the WO3 dissolution ratio was practically independent of stirring speed, while it increased with increasing the reaction temperature, and the concentrations of sodium hydroxide and phosphate. The experimental data were consistent with the shrinking core model, with a surface chemical reaction as the leaching rate-determining step. The apparent activation energy was calculated as 49.56 kJ/mol, and the reaction orders with respect to the concentrations of sodium hydroxide and phosphate were determined as 0.27 and 0.67, respectively. The kinetics equation of the leaching process was established.

Desiliconization kinetics of nickeliferous laterite ores in molten sodium hydroxide system

A novel process was proposed for treating nickeliferous laterite ores with molten sodium hydroxide.The effect on silicon extraction caused by the factors,such as stirring speed,reaction temperature,particle size and NaOH-to-ore mass ratio,was investigated.The results show that increasing stirring speed,reaction temperature and NaOH-to-ore mass ratio while decreasing particle size increases silicon extraction rate.The desiliconization kinetics of nickeliferous laterite ores in molten sodium hydroxide system was described successfully by chemical reaction control model.The activation energy of the desiliconization process was found to be 44.01 kJ/mol,and the reaction rate based on a chemical reaction-controlled process can be expressed as:1-(1-α) 1/3 = 27.67exp[-44 010/(RT)]t.

Cementing properties of steel slag activated by sodium silicates and sodium hydroxide

Steel slag which is mainly composed of γ-Ca2SiO4 and other silicates or alumino-silicates is activated by sodium sificates and sodium hydroxide. The powders of such steel slag are usually inert to hydrate and subsequently have very low ability of cementing. But when sodium silicates and sodium hydroxide are used as activators the steel slag shows very good properties of cementing. When activated with NaOH solution the hardened slurry of the steel slag has a compressive strength of 11.13 MPa after being cured for 28 days. When activated with Na2SiO3 solution the samples after being cured for 28 days have an average compres- sive strength of 40.23 MPa. While the steel slag slurry which is only mixed with water has a compressive of 0.88 MPa after being cured for 28 days.

Kinetics and leaching behaviors of aluminum from pharmaceutical blisters in sodium hydroxide solution

A hydrometallurgical process was developed for recycling pharmaceutical blisters.Leaching aluminum from pharmaceutical blisters using sodium hydroxide(NaOH) solutions was investigated with respect to leaching behaviors and kinetics.AL9(34) orthogonal design of experiments suggests that the most significant factor is NaOH concentration followed by temperature and leaching time.Factorial experiments demonstrate that the leaching rate of aluminum increases with increasing of the factors.The optimum conditions are temperature of 70 °C,leaching time of 20 min,NaOH concentration of 1.25 mol/L,liquid-to-solid mass ratio of 15:1 and agitation speed of 400 r/min.Under optimum conditions,the leaching rate is up to 100%,implying that aluminum and polyvinyl chloride(PVC) plastic in pharmaceutical blisters are separated completely.Kinetics of leaching aluminum is best described by the product layer diffusion control model,and the activation energy is calculated to be 19.26 kJ/mol.

Effect of Sodium Hydroxide on the Properties of Phosphogypsum based Cement

The effect of sodium hydroxide （NaOH） amount on phosphogypsum based cement was investigated. The mechanical performances and hydration mechanism of the phosphogypsum-based cement with different proportions of NaOH and steel slag were analyzed based on setting time, volume stability, strength test, XRD and SEM analyses. The experimental results show that, NaOH as an alkali activator significantly reduces the cement setting time and improves the cement early strength. But the acceleration of hydration proces produces coarse crystalline hydration products and the osteoporosis structure of hardened paste, which has a negative effect on later age strength. The combination of 1% NaOH and 5% steel slag as alkali activating agents is optimal with respect to early and later age strengths. Overdose of NaOH not only decreases the cement strength at later age, but also may cause problem of volume stability.

Role of hydrazine and hydrogen peroxide in aluminium hydroxide precipitation from sodium aluminate solution

Aluminium hydroxide precipitation from synthetic sodium aluminate solution was studied in the presence of hydrazine or hydrogen peroxide. The addition of low concentration of hydrazine is found to be effective, while higher amount of hydrogen peroxide is required to generate similar effect. XRD data confirm the product phase to be gibbsitic by nature. The scanning electron micrographs （SEM） show that agglomerated products form in the presence of hydrazine while fine discrete particles are produced with hydrogen peroxide. The probable mechanism of precipitation in the presence of hydrazine and hydrogen peroxide is also discussed.

Desilication kinetics of calcined boron mud in molten sodium hydroxide media

Desilication kinetics of calcined boron mud(CBM) occurring in molten sodium hydroxide media was investigated. The effects of factors such as reaction temperature and Na OH-to-CBM mass ratio on silicon extraction efficiency were studied. The results show that silicon extraction efficiency increases with increasing the reaction time and Na OH-to-CBM mass ratio. There are two stages for the desilication process of the calcined boron mud. The overall desilication process follows the shrinking-core model, and the first and second stages of the process were determined to obey the shrinking-core model for surface chemical reaction and the diffusion through the product layer, respectively. The activation energies of the first and second stages were calculated to be 44.78 k J/mol and 15.94 k J/mol, respectively.

Preparation of Spherical Silica-supported Biosorbent for Copper Ions Removal in Wastewater Based on Sol-gel Reaction and Simple Treatment with Sodium Hydroxide

A new and effective strategy was proposed for preparing new organic-inorganic composite biosorbent with spherical silica as supporting core and chitosan（CS）-based hybrid layer as shell based on sol-gel reaction and simple treatment with sodium hydroxide（NaOH）. The coating layer was covalently bound on the supporting silica through polysaccharide incorporated sol-gel process starting from CS and inorganic precursor γ-glycidoxypropyltrimethoxysiloxane（GPTMS）. GPTMS had epoxide groups and cross-linked amine groups of CS to avoid its acidic solubilization. The composite biosorbent had coarse surface due to the wet phase-inversion by treating in NaOH solution. The prepared biosorbent could be used in treating electric plating wastewater.

Corundum dissolution in concentrated sodium hydroxide solution

The corundum(α-alumina) core has been considered as a suitable candidate for investment casting of hollow, high pressure turbine engine airfoils due to its excellent properties. However, the efficiency of removing alumina cores in concentrated caustic solution cannot meet the needs of industrial production. In this paper, the effects of temperature and initial solution concentration on dissolution of α-alumina were studied by the classical weight-loss method. The fractal kinetic model was developed in order to describe α-alumina dissolution, assuming that the nonporous particles shrank during reaction process. The results show that the dissolution rate increases with increasing reaction temperature and initial solution concentration. Especially, the initial solution concentration has a significant influence on α-alumina dissolution rate at a higher reaction temperature. The activation energies decrease with increasing initial solution concentration, and the chemical reaction is the rate-controlling step.

Influence of Sodium Carbonate Amount on Crystalline Phase and Structure Stability for Doping Nickel Hydroxide

Alpha nickel hydroxide has better performances than commercial beta nickel hydroxide. However, the main defect is that α-phase is difficult to synthesize and easily transformed to β-phase Ni（OH）2 upon aging in a strong alkaline solution. In this study, the Al-Co, Al-Yb, Yb-Co and Al-Yb-Co multiple doping was used respectively. By controlling the amount of sodium carbonate, the α-Ni（OH）2 was prepared by ultrasonic-assisted precipitation. And the influence of sodium carbonate on the crystalline phase and structure stability for alpha nickel hydroxide was studied. The results demonstrate that, with increasing amount, the biphase nickel hydroxide transforms to pure alpha nickel hydroxide gradually, and the structure stability is also improved. When the amount of sodium carbonate is 2 g, the sample still keeps α-Ni（OH）2 after being aged for 30 days, for Al-Yb-Co-Ni（OH）2. And when the amount is less than 2 g, the phase transformations exist in the samples with different extents. These results demonstrated that the amount of sodium carbonate is a critical factor to maintain the structural stability of α-Ni（OH）2.

STUDIES ON THE REACTION OF SULFUR,SELENIUM AND TELLURIUM WITH SODIUM HYDROXIDE UNDER PHASE TRANSFER CATALYSIS(Ⅱ).A CONVENIENT METHOD FOR THE SYNTHESIS OF BI(ACYL)DISULFIDES

A simple and general method for the synthesis of bi(acyl)disulfides is reported.Sulfur is allowed to react with sodium hydroxide to give sodium disulfide at 65℃ under PTC,which can react with acyl halides to afford bi(acyl)disulfides in good to excellent isolated yields.The effects of solvents and phase transfer catalysts are discussed.

Secondary Crystallization of Na_2CO_3-Modified HZSM-5 Zeolites with Tetrapropylammonium Hydroxide and Their Catalytic Performance in Thiophene Alkylation Reaction

The Na2CO3-modified HZSM-5 zeolites were further treated by tetrapropylammonium hydroxide(TPAOH) solution. The effect of TPAOH concentration on the secondary crystallization process was investigated. The resulting samples were characterized by a complementary combination of X-ray diffraction, N2 adsorption/desorption, scanning electron microscopy, X-ray fluorescence spectroscopy, XPS, 27 Al and 29 Si magic-angle spinning nuclear magnetic resonance spectroscopy, BET and temperature-programmed desorption techniques. The results showed that the secondary crystallization of the HZSM-5 zeolite could result in migration of non-framework species from the internal channels to the zeolite surface and their transformation into framework species. The catalytic activity of these modified samples for thiophene alkylation was evaluated. Both the activity and stability of the catalysts were improved after secondary crystallization.

Synthesis and Characterization of Proton-conducting Polymer Electrolytes Based on Acrylonitrile-Styrene Sulfonic Acid Copolymer/Layered Double Hydroxides Nanocomposltes

Acrylonitrile-sodium styrene sulfonate copolymer/layered double hydroxides nanocomposites were prepared by in situ aqueous precipitation copolymerization of acrylonitrile （AN） and sodium styrene sulfonate （SSS） in the presence of 4-vinylbenzene sulfonate intercalated layered double hydroxides （MgA1-VBS LDHs） and transferred to acrylonitrile-styrene sulfonic acid （AN-SSA） copolymer/LDHs nanocomposites as a proton-conducting polymer electrolyte. MgA1-VBS LDHs were prepared by a coprecipitation method, and the structure and composition of MgAl-VBS LDHs were determined by X-ray diffraction （XRD）, infrared spectroscopy, and elemental analysis. X-ray diffraction result of AN-SSS copolymer/LDHs nanocomposites indicated that the LDHs layers were well dispersed in the AN-SSS copolymer matrix. All the AN-SSS copolymer/LDHs nanocomposites showed significant enhancement of the decomposition temperatures compared with the pristine AN-SSS copolymer, as identified by the thermogravimetric analysis. The methanol crossover was decreased and the proton conductivity was highly enhanced for the AN-SSA copolymer/LDHs nanocomposite electrolyte systems. In the case of the nanocomposite electrolyte containing 2% （by mass） LDHs, the proton conductivity of 2.60×10^- 3 S·m^-1 was achieved for the polymer electrolyte.

Preparation of sodium molybdate from molybdenum concentrate by microwave roasting and alkali leaching

The preparation process of sodium molybdate has the disadvantages of high energy consumption,low thermal efficiency,and high raw material requirement of molybdenum trioxide,in order to realize the green and efficient development of molybdenum concentrate resources,this paper proposes a new process for efficient recovery of molybdenum from molybdenum concentrate and preparation of sodium molybdate by microwave-enhanced roasting and alkali leaching.Thermodynamic analysis indicated the feasibility of oxidation roasting of molybdenum concentrate.The effects of roasting temperature,holding time,and power-to-mass ratio on the oxidation product and leaching product sodium molybdate (Na_(2)MoO_(4)·2H_(2)O) were investigated.Under the optimal process conditions:roasting temperature of 700℃,holding time of 110 min,and power-to-mass ratio of 110 W/g,the molybdenum state of existence was converted from MoS_(2) to Mo O3.The process of preparing sodium molybdate by alkali leaching of molybdenum calcine was investigated,the optimal leaching conditions include a solution concentration of 2.5 mol/L,a liquid-to-solid ratio of 2 mL/g,a leaching temperature of 60℃,and leaching solution termination at pH 8.The optimum conditions result in a leaching rate of sodium molybdate of 96.24%.Meanwhile,the content of sodium molybdate reaches 94.08wt%after leaching and removing impurities.Iron and aluminum impurities can be effectively separated by adjusting the pH of the leaching solution with sodium carbonate solution.This research avoids the shortcomings of the traditional process and utilizes the advantages of microwave metallurgy to prepare high-quality sodium molybdate,which provides a new idea for the highvalue utilization of molybdenum concentrate.

NaOH处理玉米秸秆厌氧生物气化试验研究(英文)

提出通过NaOH化学处理以改善玉米秸秆的可生物消化性能、提高玉米秸秆厌氧消化产气量的方法。NaOH添加量为玉米秸秆干物质的8%。对未处理和经NaOH处理的玉米秸秆进行了厌氧消化对比试验研究,厌氧消化负荷率为35,50,65和80g/L。分析并比较了两者在不同负荷率下的日产气量、累积产气量、单位TS和VS产气量等。结果显示,与未处理玉米秸相比,NaOH处理过的玉米秸的干物质消化率和产气量明显提高,在35,50,65,80g/L负荷率下,产气量分别提高了13.1%,39.8%,48.3%和47.8%,单位TS、VS的产气率分别提高了13.1%～48.3%、23%～61.3%;两种玉米秸分别在35和65g/L负荷率下获得了最高单位TS产气量。NaOH化学处理使玉米秸细胞壁结构和化学成分发生了明显的变化,分别有53.2%、46.9%和66.6%的木质素、纤维素和半纤维素被分解,其中1/2～2/3被转化成了易被厌氧菌利用的可溶性物质,这是产气量提高的主要原因之一。研究结果对提高玉米秸的产气效率、实现大规模应用具有重要指导意义。

NaOH预处理花生壳厌氧发酵制取沼气的试验研究

为了探索花生壳厌氧发酵制取沼气的产气特性和潜力,利用NaOH在无流动水和常温的条件下,分别用质量分数为2%、4%、6%、8%的NaOH溶液对花生壳进行了碱性化学预处理,在中温(35±1)℃、总固TS质量分数为8%、pH为7.0～7.6条件下,利用自行设计的厌氧发酵实验装置进行批量厌氧消化试验,研究NaOH预处理对花生壳厌氧发酵过程中产气量、pH值和甲烷含量的影响规律。结果表明,4%NaOH预处理下的花生壳的总产气量为28083mL,比不使用NaOH和8%NaOH预处理的总产气量分别高48.91%和35.72%;甲烷含量最高超过60%,且平均甲烷含量高于不处理、2%和8%NaOH预处理;pH初期波动,13d后基本稳定在7.2左右。4%NaOH预处理下的TS产气率、VS产气率以及甲烷含量和不处理以及8%NaOH预处理下的差异性显著(P<0.05),和其他两组试验之间的差异不显著(P>0.05),表明4%NaOH预处理是较优的工艺条件。

NaOH固态化学预处理对麦秸沼气发酵效率的影响研究

采用NaOH对麦秸进行固态化学预处理以提高麦秸的厌氧消化效率和产气量,并对不同负荷率下麦秸的产气情况进行了试验研究。结果表明,经4%～10%(以麦秸干重计)NaOH预处理过的麦秸的总产气量、单位TS产气量、TS和VS去除率显著提高,厌氧消化时间最大可缩短22d。其中,经6%NaOH预处理后的麦秸在65g·L-1负荷率下的单位TS产气量最高,为380.9mL·g-1,与未处理麦秸相比,提高了49.9%,厌氧消化时间缩短了19d。说明NaOH固态化学预处理是一种提高麦秸厌氧消化效率和产气量的有效方法。

红土镍矿在NaOH亚熔盐体系中的预脱硅

研究常压下高浓度氢氧化钠浸取红土镍矿的预脱硅过程,考察搅拌强度、液固比、氢氧化钠浓度、反应温度和原矿粒径对红土镍矿中硅的反应率的影响。结果表明:二氧化硅的反应率受克-金-布产物层固膜扩散控制,并由阿累尼乌斯方程得到反应的表观活化能为53.74kJ/mol。结合动力学实验结果和电子扫描电镜(SEM)及X射线能谱(EDAX)分析,证明在反应过程中通过固相产物层的内扩散为反应过程的控制步骤。