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Two lab scale upflow anaerobic sludge bed (UASB) reactors were operated at an organic loading rate of COD 9 kg x (m3 x d)(-1) to treat two kinds of calcium containing wastewaters, one of which took acetic acid as substrate and for the other, glucose and soluble starch were the substrate. Both the wastewaters contained 800 mg x L(-1) Ca+. Precipitation of calcium carbonate in the reactors was observed. The results showed that the kind of substrate had great influence on calcium carbonate precipitation. In the reactor treating acetic acid containing wastewater, a maximum calcium precipitation rate of 65% was achieved and an average rate of about 25% was then maintained. In contrast, the calcium precipitation rate for the glucose and soluble starch containing wastewater was only about 7.5%. It was also found that substantial precipitation only occurred 30 days after the reactor were operated for both of the wastewaters. After 180 days of operation, the ash content of the sludge in the reactors increased from about 10% to 70% for the acetic acid containing wastewater and 30% for the other. However, the increase of ash content had no negative influence on the COD removal efficiency, which was kept at about 90% throughout the experimental period. By the SEM it was inferred that the different substrates caused the differences of the granular sludge microstructure, leading to the diversity of calcium carbonate precipitation in the two reactors.
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PMID:[Calcium carbonate precipitation in UASB reactors with different substrates]. 1943 35

The study reports the preparation of activated carbon with a high surface area from rice husk using chemical activation with H(3)PO(4) and ZnCl(2). Activated carbon prepared from rice husk usually exhibits low specific surface areas due to its high ash content. However, experimental results show that base-leaching and acid-washing processes can effectively enhance the adsorption capacity of rice-husk carbon. The study also investigates the effects of preparation parameters on the surface characteristics of the carbon. These parameters include the kind of activating agent, before and after treatment procedures, impregnation ratio and activation temperature. The chemical and physical properties of samples were examined by EA, ICP-MS, XRD, FTIR, SEM and a N(2)-adsorption meter. The surface areas obtained from ZnCl(2) and H(3)PO(4) activation are as high as 2434 and 1741 m(2)/g, respectively. These values are higher than that of activated carbon treated with neither base nor acid (1262 and 508 m(2)/g for ZnCl(2) and H(3)PO(4) activation). Thermogravimetric analysis shows that the activation process can be divided into three parts based on temperature zones. The results of this study will be useful in developing resource recovery systems for agricultural biomass.
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PMID:Characteristics of microporous/mesoporous carbons prepared from rice husk under base- and acid-treated conditions. 1959 5

A novel adsorbent for arsenic (V) removal from wastewater was developed through simple chemical processes using a special iron-abundant fly ash. In the synthesis process, the inherent iron in the fly ash was rearranged and loaded on the surface of the fly ash by dissolution and precipitation processes. The adsorbent (HIOFAA) was characterized by XRD, FT-IR, SEM, LPS and BET surface area. The results showed that porous amorphous FeOOH was loaded on the surface of HIOFAA successfully. The BET surface area of HIOFAA was 22 times of those of the original fly ash, and furthermore, the mean particle size of HIOFAA increased 3 times compared to the raw fly ash, thus effectively accelerated the solid/liquid separation after the adsorptive treatment. The adsorption isotherm data could be well described by Langmuir isotherm model, and the adsorption capacity for arsenic removal was 19.46 mg g(-1). Accordingly, it is believed that the adsorbent developed in this study is effective for arsenic polluted wastewater treatment.
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PMID:Arsenic (V) removal from aqueous system using adsorbent developed from a high iron-containing fly ash. 1965 28

In this paper, the effects of fluidization velocity, bed temperature and fuel feeding rate on the defluidization time and agglomerate fraction in the fluidized bed combustion of rice straw were studied. The fuel ash, necks in agglomerates and coating layers of bed particles were studied by means of the scanning electron microscope, coupled with energy-dispersive spectroscopy (SEM/EDS). Results showed that the stickiness of bed particles induced by coating layers is the direct reason for bed defluidization. The alkali metals such as K and Na mainly exist in the outer layer of rice straw particles. During combustion the high temperature can cause the alkali species melting and coating the surfaces of ash particles. Consequently, ash particles become sticky and tend to adhere to the surfaces of bed particles. The large-sized ash particles may act as the necks in the formation of agglomerates. The small-sized ash particles may contribute to the formation of coating layers.
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PMID:The role of ash particles in the bed agglomeration during the fluidized bed combustion of rice straw. 1966 17

Bulk porous mullite supports for ceramic membranes were prepared directly using a mixture of industrial waste fly ash and bauxite by dry-pressing, followed by sintering between 1200 and 1550 degrees C. The effects of sintering temperature on the phase composition and shrinkage percent of porous mullite were studied. The XRD results indicate that secondary mullitization reaction took place above 1200 degrees C, and completed at 1450 degrees C. During sintering, the mixture samples first shrunk, then expanded abnormally between 1326 and 1477 degrees C, and finally shrunk again above 1477 degrees C. This unique volume self-expansion is ascribed to the secondary mullitization reaction between bauxite and fly ash. More especially, the micro-structural variations induced by this self-expansion sintering were verified by SEM, porosity, pore size distribution and nitrogen gas permeation flux. During self-expansion sintering, with increasing temperature, an abnormal increase in both open porosity and pore size is observed, which also results in the increase of nitrogen gas flux. The mineral-based mullite supports with increased open porosity were obtained. Furthermore, the sintered porous mullite membrane supports were characterized in terms of thermal expansion co-efficient and mechanical strength.
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PMID:Reaction-sintered porous mineral-based mullite ceramic membrane supports made from recycled materials. 1966 97

Bottom ash from a municipal solid waste incinerator on a former contaminated site, the island of Sacca San Biagio (Lagoon of Venice), was examined in order to evaluate levels of pollutants and their potential mobility and availability. Heavy metal concentrations were determined and the actual contamination of the site was compared with national legislation on polluted sites. The site was mainly contaminated by zinc, copper and lead. Physico-chemical characterization of bottom ash was carried out by SEM (Scanning Electron Microscopy) with micro-analysis by EDS (Energy Dispersive X-ray Spectroscopy) and XRD (X-ray Diffractometry), for information on newly formed minerals. SEM-EDS analysis revealed the presence of particles, compounds and clusters containing heavy metals and, in particular, the presence of barium sulfate, which was assumed to be a site-specific compound. Similarities between bottom ash and atmospheric PM10 collected on the adjacent island of Sacca Fisola were studied and a risk of aerodispersion of the fine fraction of ash was assumed. Lastly, in order to evaluate the potentially available fraction of metals (non-residual fraction) and the directly exchangeable fraction, two single extraction procedures with HCl and citric acid were carried out, respectively. Results showed a relatively low concentration of readily phyto-available metals, as well as the high concentrations found for some heavy metals (Cu, Pb, Zn) in the potentially mobilizable fraction.
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PMID:Characterization of a former dump site in the Lagoon of Venice contaminated by municipal solid waste incinerator bottom ash, and estimation of possible environmental risk. 1969 69

This work aims to develop a new mineral porous tubular membrane based on mineral coal fly ash. Finely ground mineral coal powder was calcinated at 700 degrees C for about 3 h. The elaboration of the mesoporous layer was performed by the slip-casting method using a suspension made of the mixture of fly-ash powder, water and polyvinyl alcohol (PVA). The obtained membrane was submitted to a thermal treatment which consists in drying at room temperature for 24 h then a sintering at 800 degrees C. SEM photographs indicated that the membrane surface was homogeneous and did not present any macrodefects (cracks, etc...). The average pore diameter of the active layer was 0.25 microm and the thickness was around 20 microm. The membrane permeability was 475 l/h m(2) bar. This membrane was applied to the treatment of the dying effluents generated by the washing baths in the textile industry. The performances in term of permeate flux and efficiency were determined and compared to those obtained using a commercial alumina microfiltration membrane. Almost the same stabilised permeate flux was obtained (about 100 l h(-1)m(-2)). The quality of permeate was almost the same with the two membranes: the COD and color removal was 75% and 90% respectively.
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PMID:Elaboration of new ceramic microfiltration membranes from mineral coal fly ash applied to waste water treatment. 1969 33

Polish bituminous (PB) and South African (SA) coal fly ash (FA) samples, derived from pilot-scale circulated fluidized bed (CFB) combustion facilities, were utilized as raw materials for the synthesis of zeolitic products. The two FAs underwent a hydrothermal activation with 1M NaOH solution. Two different FA/NaOH solution/ratios (50, 100g/L) were applied for each sample and several zeolitic materials were formed. The experimental products were characterized by means of X-ray diffraction (XRD) and energy dispersive X-ray coupled-scanning electron microscope (EDX/SEM), while X-ray fluorescence (XRF) was applied for the determination of their chemical composition. The zeolitic products were also evaluated in terms of their cation exchange capacity (CEC), specific surface area (SSA), specific gravity (SG), particle size distribution (PSD), pH and the range of their micro- and macroporosity. Afterwards the hybrid materials were tested for their ability of adsorbing Cr, Pb, Ni, Cu, Cd and Zn from contaminated liquids. Main parameters for the precipitation of the heavy metals, as it was concluded from the experimental results, are the mineralogical composition of the initial fly ashes, as well as the type and the amount of the produced zeolite and specifically the mechanism by which the metals ions are hold on the substrate.
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PMID:Removal of heavy metals from wastewater using CFB-coal fly ash zeolitic materials. 1976 1

A slow deposition of atmospheric components occurs on tree barks. One part of them can be incorporated into bark tissues. This work demonstrates that mineral particles are present inside the suber tissue in four-year-old ash tree stems. Most of these particles are smaller than 2 microm. Scanning electronic microscope studies - using energy dispersive X-ray spectroscopy (SEM-EDX) - on stem cuttings show that they are located either inside the dead suber cells or between these cells. Numerous particles are composed of clay, quartz, feldspar or mica. Others, clearly of anthropogenic origin, are metallic fragments composed of Fe, Ni, Cr, Pb, etc. Spherical fly ashes were found, composed of Si, Al or Fe, and demonstrating an anthropogenic formation. Such particles were isolated and purified from suber ashes obtained at 550 degrees C, after aqueous and acidic treatments, and their composition was established through SEM-EDX. These results reinforce the idea that the suber of tree barks alone can be considered as archives for atmospheric deposition.
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PMID:The inclusion of atmospheric particles into the bark suber of ash trees. 1984 95

Taiyuan, the capital of Shanxi province, China, is one of the most polluted cities in the world. To characterize the ambient particulate pollution, samples of particulates with aerodynamic diameter less than 10 microm (PM(10)) were collected during a 6-day campaign. Individual particles were analyzed by Scanning Electron Microscope with Energy-Dispersive Spectrometer (SEM-EDS) to determine their chemical composition. Meanwhile, photomicrographs were obtained from SEM to aid in particles' source identification. The lumped data from SEM-EDS were subjected to hierarchical cluster analysis (HCA) to sort out particle types chemically. HCA combined with SEM photomicrographs allowed us to identify 20 different particle types, namely (in order of particle frequency), soil/fly ash particles, coal-burning, sulfur-rich, and iron-rich particles, gypsum, syngenite, quartz, cement, silicon sulfide, siliconferro alloy, calcium-rich particles, ferrochromium alloy, ammonium sulfate and chloride, iron-zinc, ammonium chloride, molybdenum-rich, potassium sulfate, dolomite, lead sulfate, and copper-rich particles. Their possible origins and pathways are suggested. The majority of the particles seem to originate from coal combustion, which conforms to Taiyuan's industrial structure.
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PMID:Characterization of individual airborne particles in Taiyuan City, China. 1989 Apr 3


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