Simultaneous uptake of ammonium and phosphate ions by compounds prepared from paper sludge ash

Al-containing CaO-SiO(2)-H(2)O phases were prepared by hydrothermal treatment of mixtures of paper sludge ash (PSA) with various silica and calcia sources and their properties were determined with particular reference to the simultaneous uptake of ammonium and phosphate ions, which are implicated in the eutrophication of lakes and ponds. After examination of various silica and calcia sources, Ca(OH)(2) and SiO(2) sol were selected as the most appropriate starting materials. Dry milling was found to be superior to wet milling in avoiding contamination from the milling media during mixing. Nine samples with three different Ca/Si ratios and Al(2)O(3) contents were prepared with various mass ratios of Ca(OH)(2), PSA and SiO(2). The chemical compositions of the hydrothermal products of these mixtures moved towards the tieline of CaSiO(3)-PSA, with respect to the starting compositions. The major phase formed in all samples was poorly crystalline C-S-H(I), with hydroxysodalite also formed in the Al-containing mixtures. All the products showed a capacity for the simultaneous uptake of ammonium and phosphate ions. The saturated sorption capacities calculated from the Langmuir equation ranged from 0.9 to 2.4mmol/g for the ammonium ion and from 3.3 to 5.2mmol/g for the phosphate ion. Since the sorption capacities for both ions increased with increasing Ca contents of the product, substitution of Ca(2+) for NH(4)(+) and the formation of calcium phosphate phases such as apatite and brushite by precipitation are thought to be the main sorption mechanisms.     

Effective utilization of waste ash from MSW and coal co-combustion power plant: Zeolite synthesis

The solid by-product from power plant fueled with municipal solid waste and coal was used as a raw material to synthesize zeolite by fusion-hydrothermal process in order to effectively use this type of waste material. The effects of treatment conditions, including NaOH/ash ratio, operating temperature and hydrothermal reaction time, were investigated, and the product was applied to simulated wastewater treatment. The optimal conditions for zeolite X synthesis were: NaOH/ash ratio=1.2:1, fusion temperature=550 degrees C, crystallization time=6-10 h and crystallization temperature=90 degrees C. In the synthesis process, it was found that zeolite X tended to transform into zeolite HS when NaOH/ash ratio was 1.8 or higher, crystallization time was 14-18 h, operating temperature was 130 degrees C or higher. The CEC value, BET surface area and pore volume for the synthesized product at optimal conditions were 250 cmol kg(-1), 249 m(2) g(-1) and 0.46 cm(3) g(-1) respectively, higher than coal fly ash based zeolite. Furthermore, when applied to Zn(2+) contaminated wastewater treatment, the synthesized product presented larger adsorption capacity and bond energy than coal fly ash based zeolite, and the adsorption isotherm data could be well described by Langmuir and Freundlich isotherm models. These results demonstrated that the special type of co-combustion ash from power plant is suitable for synthesizing high quality zeolite, and the products are suitable for heavy metal removal from wastewater.     

ZnTiO3-based ceramics sintered at low temperature with boron addition for multilayer ceramic capacitor applications

Mixture of zinc metatitanate and rutile (ZnTiO₃ + 0.2TiO₂), had been prepared via the conventional solid-state reaction method. The sintering behavior and microwave dielectric properties of ZnO–TiO₂ system were investigated. The composition and microstructure of ceramics were discussed with XRD and SEM. It was found that ZnO–TiO₂ ceramics, which was sintered at 900°C using 1.0 wt% B₂O₃ as sintering additive, had homogeneously fine microstructures and high densification. Samples possessed excellent microwave dielectric properties: ε _r = 26, Q × f = 34,890 GHz, and τ _f = ?11 ppm/°C. The above- mentioned material was suitable for the tape casting process and compatible with Ag electrodes, therefore, was an excellent candidate for multilayer ceramic capacitor applications.     

Ni/Ni3C core-shell nanochains and its magnetic properties: one-step synthesis at low temperature

One-dimensional Ni/Ni3C core-shell nanoball chains with an average diameter by around 30 nm were synthesized by means of a mild chemical solution method using a soft template of trioctylphosphine oxide (TOPO). It was revealed that the uniform Ni nanochains were capped with Ni3C thin shells by about 1-4 nm in thickness and each Ni core consists of polygrains. The coercivity of the core-shell nanochains is much enhanced (600 Oe at 5 K) and comparable with single Ni nanowires due to the one-dimensional shape anisotropy. Deriving from the distinctive structure of Ni core and Ni 3C shell, this architecture may possess a possible bifunctionality. This unique architecture is also useful for the study on the magnetization reversal mechanism of one-dimensional magnetic nanostructure.     

Facile chemical synthesis of W-Ag and W-Cu nanocomposites at low temperature

W-Ag (80.2W-19.8Ag, 70.4W-29.6Ag and 60.5W-39.5Ag) and W-Cu (79.7W-20.3Cu, 70.5W-29.5Cu and 59.8W-40.2Cu) nanocomposites in the size range of 24-30 nm have been synthesized by thermal decomposition of W(CO)6/CH3COOAg and W(CO)6/Cu(acac)2 in diphenyl ether as solvent at 220 degrees C in presence of oleic acid and hexadecyl amine and characterized. FTIR spectra have been used to explain the role of oleic acid and hexadecyl amine in the synthesis of W-Ag and W-Cu composite powders. XRD studies show that the tungsten phase is amorphous, whereas both Ag and Cu crystallize in fcc for as-synthesized W-Ag and W-Cu nanocomposites. These composite powders when annealed at 700 degrees C results in the formation of bcc tungsten and peaks corresponding to fcc silver and copper still persists. The particle size, shape and distribution of these nanocomposites of various compositions have been studied by SAXS, ESEM and TEM and found to be nearly spherical with the average diameters below 30 nm.     

Low pressure polymer precursor for synthesis of diamond at low temperature

Abstracts are not published in this journal     

One step synthesis of rutile TiO2 nanoparticles at low temperature

Sphere-like rutile TiO2 nanocrystals have been synthesized by sol-gel method followed by hydrolysis of titanium tetrachloride in deionized water in the presence of ammonium hydroxide as hydrolysis catalyst. The as-prepared TiO2 nanoparticles have single rutile phase with average diameter approximately 26.4 nm. The results show that the temperature has a great influence on the particle size distribution and also crystalline phase (rutile) of TiO2 nanoparticles is consistent with the temperature. Characterization of the as-prepared nanocrystalline powder was carried out by different techniques such as powder X-ray diffraction (XRD), field emission transmission electron microscopy (FE-TEM) and Raman spectroscopy.     

Low pressure polymer precursor for synthesis of diamond at low temperature

Abstracts are not published in this journal This revised version was published online in November 2006 with corrections to the Cover Date.     

Performance evaluation of a mesophilic (37 degrees C) upflow anaerobic sludge blanket reactor in treating distiller's grains wastewater

The performance of a laboratory-scale upflow anaerobic sludge blanket (UASB) reactor treating distiller's grains wastewater was investigated for 420 days at 37 degrees C. After a successful start-up, 80-97.3% chemical oxygen demand (COD) removal efficiencies were achieved at hydraulic retention times (HRT) of 82-11h with organic loading rates (OLR) of 5-48.3kgCODm(-3)d(-1). The biogas mainly consisted of methane and carbon dioxide, and the methane and carbon dioxide content in the biogas was 57-60 and 38-41%, respectively. The yield coefficient of methane production was 0.3182lCH(4)g(-1)COD removed until OLR at 33.3kgCODm(-3)d(-1), but afterwards began to decrease. The volatile fatty acid (VFA) in the effluent mainly consisted of acetate and propionate, accounting for more than 95% of total VFA as COD, and other VFA was detected at insignificant concentrations. The mesophilic granules developed in this study showed an excellent specific methanogenic activity (SMA) at 0.91 and 1.12gmethaneCODg(-1)VSS(-1)d(-1) using sucrose and acetate as individual substrates on day 200, respectively.     

Evaluation of various additives on the preparation of rice husk ash (RHA)/CaO-based sorbent for flue gas desulfurization (FGD) at low temperature

This paper examines the effectiveness of 10 additives toward improving SO2 sorption capacities (SSC) of rice husk ash (RHA)/lime (CaO) sorbent. The additives examined are NaOH, CaCl2, LiCl, NaHCO3, NaBr, BaCl2, KOH, K2HPO4, FeCl3 and MgCl2. Most of the additives tested increased the SSC of RHA/CaO sorbent, whereby NaOH gave highest SSC (30mg SO2/g sorbent) at optimum concentration (0.25mol/l) compared to other additives examined. The SSC of RHA/CaO sorbent prepared with NaOH addition was also increases from 17.2 to 39.5mg SO2/g sorbent as the water vapor increases from 0% RH to 80% RH. This is probably due to the fact that most of additives tested act as deliquescent material, and its existence increases the amount of water collected on the surface of the sorbent, which played an important role in the reaction between the dry-type sorbent and SO2. Although most of the additives were shown to have positive effect on the SSC of the RHA/CaO sorbent, some were found to have negative or insignificant effect. Thus, this study demonstrates that proper selection of additives can improve the SSC of RHA/CaO sorbent significantly.     

Starch-stabilized synthesis of ZnO nanopowders at low temperature and optical properties study

Zinc oxide nanoparticles (ZnO–NPs) were synthesized via the sol–gel method in starch media. Starch was used as a stabilizer to control of the mobility of zinc cations and then control growth of the ZnO–NPs. Because of the special structure of the starch, it permits termination of the particle growth. Thermogravimetry analysis (TGA) was applied on dried gel to obtain the certain calcination temperature(s) of the ZnO–NPs. The dried gel was calcined at different temperatures of 400, 500, and 600 °C. Several techniques such as X-ray diffraction analysis (XRD), Fourier transform infrared spectroscopy (FTIR), and high-magnification transmission electron microscopy (TEM) were used to characterize the ZnO–NPs. The ZnO–NPs calcined at different temperatures exhibited a hexagonal (wurtzite) structure with sizes from 30 to 50 nm. The optical properties of the prepared samples were investigated using UV–vis spectroscopy. The results showed that starch is a suitable stabilizer in the sol–gel technique, and this method is a reasonable and facile method to prepare ZnO–NPs for large-scale production.     

In situ synthesis of bone-like apatite/collagen nano-composite at low temperature

A nano-composite of bone-like apatite/collagen was prepared by a new method—low-temperature in situ synthesis using calcium nitrate, diammoniun hydrogen phosphate and cow hide collagen as starting materials. The composite was investigated via X-ray diffraction (XRD), Fourier transform infrared (FTIR), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). It was found that bone-like nanoapatite particles were distributed uniformly in collagen fibrils in the composite. The composite with homogeneous microstructure was similar to natural bone in crystallite phase composition and crystal size. The biomimetic composite is expected to exhibit desirable properties in biomedical applications.     

Solid-state reaction synthesis of sodium niobate (NaNbO<Subscript>3</Subscript>) powder at low temperature

A modified solid-state reaction was applied to produce lead-free piezoelectric sodium niobate (NaNbO₃) powders. The mixture of Na₂C₂O₄ and Nb₂O₅ was identified by thermo gravimetric analysis (TGA) and differential thermal analysis (DTA). The powders were characterized using a scanning electron microscope (SEM) and the X-ray diffraction technique (XRD). The SEM image suggested that the particle size of the powders obtained ranged from 180 to 360 nm. The XRD pattern showed that the pure perovskite phase of NaNbO₃ could be synthesized at the low temperature of 475 °C for 1 h, with an average crystallite size of 31.45 ± 5.28 nm. This temperature was about 300 °C lower than that when using the conventional solid-state method with Na₂CO₃ as reactant, which resulted in a cost-, energy-, and time-saving method.     

Effects of nickel(II) addition on the activity of activated sludge microorganisms and activated sludge process

The effects of Ni(II) in a synthetic wastewater on the activity of activated sludge microorganisms and sequencing batch reactor (SBR) treatment process were investigated. Two parallel lab-scale SBR systems were operated. One was used as a control unit, while the other received Ni(II) concentrations equal to 5 and 10 mg/l. The SBR systems were operated with FILL, REACT, SETTLE, DRAW and IDLE modes in the time ratio of 0.5:3.5:1.0:0.75:0.25 for a cycle time of 6 h. The addition of Ni(II) into SBR system caused drastically dropped in TOC removal rate (k) and specific oxygen uptake rate (SOUR) by activated sludge microorganisms due to the inhibitory effects of Ni(II) on the bioactivity of microorganisms. The addition of 5 mg/l Ni(II) caused a slight reduction in TOC removal efficiency, whereas 10 mg/l Ni(II) addition significantly affected the SBR performance in terms of suspended solids and TOC removal efficiency. Termination of Ni(II) addition led to almost full recovery of the bioactivity in microorganisms as shown in the increase of specific oxygen uptake rate (SOUR) and SBR treatment performance.     

Synthesis of magnetic nanostructures: Shape tuning by the addition of a polymer at low temperature

We report a simple method for shape-controlled synthesis of iron oxide spinels such as magnetite (Fe₃O₄) and maghemite (γ-Fe₂O₃) nanostructures using a thermoresponsive polymer poly(vinyl methyl ether) (PVME) by the alkaline hydrolysis of iron salt at low temperature (20 °C). Microscopic analysis confirmed the formation of needle- and flower-shaped iron oxide nanostructures depending on reaction conditions. High-resolution transmission electron microscopic analysis of the needle- and flower-shaped nanostructures as well as their corresponding selected area electron diffraction patterns revealed that the formed nanostructures are crystalline in nature. X-ray diffraction study reveals the formation of well-crystalline pure Fe₃O₄ and γ-Fe₂O₃ nanostructures under different reaction conditions. Fourier transform Infra-red spectroscopic analysis confirms the adsorption of PVME on the surface of iron oxide nanostructures. Finally, the magnetic properties of γ-Fe₂O₃ and Fe₃O₄ nanostructures is studied that shows the superparamagnetic behavior of the formed iron oxide nanostructures.     

Chemical synthesis and low temperature electrical transport in polypyrrole doped with sodium bis(2-ethylhexyl) sulfosuccinate

Polypyrrole (PPy) is polymerized by chemical oxidative polymerization in presence of anionic surfactant sodium bis (2-ethylhexyl) sulfosuccinate (DEHS) as the dopant. The electrical conductivity was optimized in terms of oxidant to monomer molar ratio and polymerization yield was measured for these reactions. We have used ammonium persulphate (APS) as the oxidant for polymerization in this series of experiments. The effect of concentration of oxidant on the electrical conductivity is examined. Chemical synthesis of polypyrrole is supported by FTIR spectrum. The electrical conductivity of doped and undoped polypyrrole has been measured in the temperature range of 10–300 K and is found to increase with rise in temperature. Electrical conductivity of PPy was analyzed in the light of various charge transport models. Analysis of the electrical conductivity data reveals that in the temperature range 60–300 K electrical transport is predominantly governed by power law behaviour given by Kivelson model. However in the low temperature range 10–60 K electrical transport is dominated by the fluctuation assisted mechanism.     

Modelling of C(2) addition route to the formation of C(60)

To understand the phenomenon of fullerene growth during its synthesis, an attempt is made to model a minimum energy growth route using a semi-empirical quantum mechanics code. C(2) addition leading to C(60) was modelled and three main routes, i.e.?cyclic ring growth, pentagon and fullerene road, were studied. The growth starts with linear chains and, at n = 10, ring structures begins to dominate. The rings continue to grow and, at some point n>30, they transform into close-cage fullerenes and the growth is shown to progress by the fullerene road until C(60) is formed. The computer simulations predict a transition from a C(38) ring to fullerene. Other growth mechanisms could also occur in the energetic environment commonly encountered in fullerene synthesis, but our purpose was to identify a minimal energy route which is the most probable structure. Our results also indicate that, at n = 20, the corannulene structure is energetically more stable than the corresponding fullerene and graphene sheet, however a ring structure has lower energy among all the structures up to n≤40. Additionally, we have also proved that the fullerene road is energetically more favoured than the pentagon road. The overall growth leading to cage closure for n = 60 may not occur by a single route but by a combination of more than one route.     

Growth of few layer graphene from commercial C2 hydrocarbons at low temperature and controlled surface functionalization

Graphene is mostly grown from methane on copper foils at a high temperature about 1000°C. In this research, a commercial ethylene-acetylene-ethane mixture was used as a clean precursor for graphene synthesis on nickel foils in a chemical vapor deposition reactor at 750°C. Furthermore, controlled functionalization of graphene sheets was achieved via hydrothermal oxidation at moderate pressure and temperature using nitric acid. Broadened 2D band and G band frequencies in Raman spectra indicated that pristine graphene (PG) was of high quality with low defects. X-ray diffraction results confirmed that PG has five layers. Transmission electron microscopy and N₂ adsorption-desorption analyses affirmed that the graphene is of a good quality, large surface area (562 m²/g) and small pore size. Fourier transform infrared spectroscopy confirmed functionalization process performance. Thermogravimetric analysis affirmed that the thermal stability of PG was drastically decreased after the functionalization process.     

Kinetics and thermodynamics of adsorption of azinphosmethyl from aqueous solution onto pyrolyzed (at 600 degrees C) ocean peat moss (Sphagnum sp.)

The removal of azinphosmethyl from aqueous solution onto pyrolyzed ocean peat moss (Sphagnum sp.), as a residue, from the Rhode Island coast (USA), has been investigated at different temperatures and initial concentrations. The ocean peat moss had been pyrolyzed at 600 degrees C in nitrogen atmosphere before the adsorption process. The kinetic data obtained from batch studies have been analyzed using pseudo-first order kinetic model. The rate constants were evaluated at different temperatures. The thermodynamic parameters (DeltaG degrees , DeltaH degrees , DeltaS degrees ) for the adsorption process were calculated and the results suggest that the nature of adsorption is endothermic and the process is spontaneous and favorable. The activation energy for adsorption process was estimated, about 18.3 kJ mol(-1). According to this value the adsorption of azinphosmethyl onto pyrolyzed ocean peat moss is in the range of physical adsorption. The experimental data have been modeled using Langmuir, Freundlich and Temkin isotherms. It was found that Langmuir and Freundlich isotherms give the best correlation with the experimental data.