Corrosion of carbon steel in filling material in an urban environment

The corrosion process of carbon steel in soil has been investigated, in particular the influence of the soil of an urban environment. A field test was carried out with test panels buried in trenches. Localized and uniform corrosion rates were evaluated after 1 and 3 years. Soil samples from points adjacent to the panels were analyzed with respect to a number of physical and chemical parameters believed to influence the corrosion process. Corrosion products were analyzed and identified. The study shows that the localized corrosion rate of soil buried constructions may be remarkably high in a filling material in comparison to other soils. The heterogeneity of the soil seems to have a greater influence on the localized corrosion rate than the chemical composition of the soil. However, the uniform corrosion rate was comparatively low in the heterogeneous filling material. Both the high alkalinity in the soil water and the groundwater, and the high total hardness of the soil water in the filling material seem to reduce the uniform corrosion rate. Corrosion rate determinations with commercial probes is also discussed. The linear polarization resistance (LPR), the electric resistance (ER) and the corrosion potential measurement techniques are compared. All probes showed a seasonal variation in corrosion rate. The measurements with commercial probes were associated with some problems, mostly a result of poor contact between the probes and the soil.     

Reorganization of the Brain Extracellular Matrix in Hippocampal Sclerosis

The extracellular matrix (ECM) is an important regulator of excitability and synaptic plasticity, especially in its highly condensed form, the perineuronal nets (PNN). In patients with drug-resistant mesial temporal lobe epilepsy (MTLE), hippocampal sclerosis type 1 (HS1) is the most common histopathological finding. This study aimed to evaluate the ECM profile of HS1 in surgically treated drug-resistant patients with MTLE in correlation to clinical findings. Hippocampal sections were immunohistochemically stained for aggrecan, neurocan, versican, chondroitin-sulfate (CS56), fibronectin, Wisteria floribunda agglutinin (WFA), a nuclear neuronal marker (NeuN), parvalbumin (PV), and glial-fibrillary-acidic-protein (GFAP). In HS1, besides the reduced number of neurons and astrogliosis, we found a significantly changed expression pattern of versican, neurocan, aggrecan, WFA-specific glycosylation, and a reduced number of PNNs. Patients with a lower number of epileptic episodes had a less intense diffuse WFA staining in Cornu Ammonis (CA) fields. Our findings suggest that PNN reduction, changed ECM protein, and glycosylation expression pattern in HS1 might be involved in the pathogenesis and persistence of drug-resistant MTLE by contributing to the increase of CA pyramidal neurons’ excitability. This research corroborates the validity of ECM molecules and their modulators as a potential target for the development of new therapeutic approaches to drug-resistant epilepsy.     

Toward understanding the efficacy and mechanism of Opuntia spp. as a natural coagulant for potential application in water treatment

Historically, there is evidence to suggest that communities in the developing world have used plant-based materials as one strategy for purifying drinking water. In this study, the coagulant properties of Opuntia spp., a species of cactus, are quantitatively evaluated for the first time. Opuntia spp. was evaluated for turbidity removal from synthetic water samples, and steps were made toward elucidating the underlying coagulation mechanism. In model turbid water using kaolin clay particles at pH 10, Opuntia spp. reduced turbidity by 98% for a range of initial turbidities. This is similar to the observed coagulation activities previously described for Moringa oleifera, a widely studied natural coagulant. Although it has been reported that Moringa oleifera predominantly operates through charge neutralization, comparison of zeta potential measurements and transmission electron microscopy images of flocs formed by Opuntia spp. suggest that these natural coagulants operate through different mechanisms. It is suggested that Opuntia spp. operates predominantly through a bridging coagulation mechanism. Once optimized, application of these readily available plants as a part of point-of-use water treatment technology may offer a practical, inexpensive, and appropriate solution for producing potable water in some developing communities.     

Comparative Study between a Hybrid System and a Biofilm System for the Treatment of Ammonia and Organic Matter in Wastewaters

The efficiency of two similar gas-lift bioreactors, a biofilm reactor and a hybrid circulating floating bed reactor (CFBR), were studied and compared. In the biofilm CFBR the biomass grew preferably adhered on a plastic granular support, whereas in the hybrid CFBR both suspended biomass and biofilms were allowed to grow in the reactor. COD/NH4+ ratio (COD=chemical oxygen demand) was manipulated between 0.0 and 8.0?g/g, maintaining the ammonia influent concentration around 50?mg N–NH4+/L, the ammonia loading rate at 0.9?kg N–NH4+/m3?day and the hydraulic retention time at 1.36?h. At low COD/NH4+ ratio (0 and 0.5?g/g) both systems behaved similarly, achieving ammonia removal percentages higher than 95%. In the biofilm CFBR a reduction of the nitrification percentage from 95 to 20% was observed when a COD/N–NH4+ ratio up to 8?g/g was applied in the influent. However, at the same operational conditions, the nitrification process in the hybrid CFBR was slightly affected. In the hybrid-CFBR reactor heterotrophs growing in suspension consumed the COD source faster than those growing in biofilms as was monitored. The growth of heterotrophic microorganism in suspension had a beneficial effect for the nitrifying population growing in the biofilm of the hybrid CFBR. Nitrifying activity of the biofilm was not limited by the presence of heterotrophs consuming dissolved oxygen, displacing the nitrifying bacteria or creating mass transfer resistance as was observed in the biofilm CFBR.     

Development of a membrane‐assisted hybrid bioreactor for ammonia and COD removal in wastewaters

A new membrane‐assisted hybrid bioreactor was developed to remove ammonia and organic matter. This system was composed of a hybrid circulating bed reactor (CBR) coupled in series to an ultrafiltration membrane module for biomass separation. The growth of biomass both in suspension and biofilms was promoted in the hybrid reactor. The system was operated for 103 days, during which a constant ammonia loading rate (ALR) was fed to the system. The COD/N‐NH₄⁺ ratio was manipulated between 0 and 4, in order to study the effects of different organic matter concentrations on the nitrification capacity of the system. Experimental results have shown that it was feasible to operate with a membrane hybrid system attaining 99% chemical oxygen demand (COD) removal and ammonia conversion. The ALR was 0.92 kg N‐NH₄⁺ m^?3 d^?1 and the organic loading rate (OLR) achieved up to 3.6 kg COD m^?3 d^?1. Also, the concentration of ammonia in the effluent was low, 1 mg N‐NH₄⁺ dm^?3. Specific activity determinations have shown that there was a certain degree of segregation of nitrifiers and heterotrophs between the two biomass phases in the system. Growth of the slow‐growing nitrifiers took place preferentially in the biofilm and the fast‐growing heterotrophs grew in suspension. This fact allowed the nitrifying activity in the biofilm be maintained around 0.8 g N g^?1 protein d^?1, regardless of the addition of organic matter in the influent. The specific nitrifying activity of suspended biomass varied between 0.3 and 0.4 g N g^?1 VSS d^?1. Copyright © 2004 Society of Chemical Industry     

Fractionation of Sauvignon wine macromolecules by ultrafiltration and diafiltration: impact of protein composition on white wine haze stability

After ultrafiltration (UF) thermally unstable compounds of Sauvignon blanc wines were concentrated in the retentate fractions of 10–30 kDa increasing heat‐induced haze 8.9‐fold, while concentrating haze stabilising species into the retentate fractions of 100–300 kDa with a 5.3‐fold reduction of heat‐induced haze compared to unfiltered wine. Proteins having molecular weights of 18, 23, 33, 35, 40 and 60 kDa were identified as the main haze promoting agents for Sauvignon blanc, where the proteins of 56, 69 and 72 kDa were identified as thermally stable. Potassium sulphate (100 mg L^?1) and magnesium sulphate (25 mg L^?1) did not affect wine haziness at experimental diafiltration (DF) conditions using model wine solutions. Combination of UF and DF is a useful separation method of wine proteins, which is helpful to quantify haziness of individual species and to reveal the interactions between species involving protein haze.     

Ceramic Filters Impregnated with Silver Nanoparticles for Point-of-Use Water Treatment in Rural Guatemala

The technological performance and social acceptance of ceramic water filters impregnated with silver nanoparticles for point-of-use water treatment were investigated in the laboratory and in the field in the Guatemalan highland community of San Mateo Ixtatán. In the laboratory, filters were constructed with clay and sawdust collected from the Guatemalan community and were tested to determine the effects of percent sawdust and silver nanoparticle treatment on the transport and removal of E. coli. For ceramic filters without silver treatment, size-exclusion and/or sorption is the mechanism of removal and a lower mass-percent sawdust corresponds to greater bacteria removal. The addition of silver nanoparticles to the ceramic filters improved the performance for all mass percentages of sawdust relative to filter media without nanoparticle treatment. Filters with higher porosity achieved higher bacteria removal than those with lower porosity, suggesting an increase in burnable material percentage is advantageous, assuming structural integrity is not compromised. Subsequent to laboratory testing, ceramic filters were manufactured with local materials and labor in San Mateo Ixtatán, Guatemala, and distributed to 62 households in this peri-urban community. The study participants were randomly divided into two groups, and filters were tested periodically over 23?months or 12?months. Filtered effluent samples were tested for turbidity reduction, bacteria removal, and silver leaching. Over the course of the study, the average percent reduction in total coliforms and E. coli was 87% and 92%, respectively. The average effluent turbidity was 0.18 nephelometric turbidity units (NTUs) and average effluent concentration of ionic silver was 0.02??mg/L (below the U.S. EPA standard of 0.1??mg/L). Filters distributed to the second study group consistently performed better than the first study group as manufacturing techniques improved and contact with researchers increased. Overall, users were satisfied with the filters, citing them as easy to use and maintain while improving water quality. The findings of this study suggest that locally manufactured ceramic filters can significantly improve the microbiological quality of water when used as a point-of-use water-treatment technology.     

Effect of quaternary ammonium cation loading and pH on heavy metal sorption to Ca bentonite and two organobentonites

Sorption of four heavy metals (Pb, Cd, Zn and Hg) to calcium bentonite (Ca bentonite), hexadecyltrimethylammonium bentonite (HDTMA bentonite) and benzyltriethylammonium bentonite (BTEA bentonite) was measured as a function of the quaternary ammonium cation (QAC) loading at 25, 50 and 100% of the clay's cation-exchange capacity (CEC). The effects of pH on the surface charge of the clays and heavy metal sorption were also measured. Sorption of Cd, Pb, and Zn was non-linear and sorption of all three metals by HDTMA and BTEA bentonites decreased as the QAC loading increased from 25 to 100%. In most cases, sorption of these metals to 25% BTEA and 25% HDTMA bentonite was similar to or greater than sorption to Ca bentonite. Hg sorption was linear for both HDTMA and BTEA bentonite. No significant effect on Hg sorption was observed with increasing QAC loading on BTEA bentonite. However, an increase of Hg sorption was detected with increasing QAC loading on HDTMA bentonite. This behavior suggests that a process different than cation exchange was the predominant Hg sorption mechanism. Cd, Pb, and Zn sorption decreased with pH. However, this effect was stronger for Cd and Pb than Zn. Hg sorption varied inversely with pH. QAC loading affected the surface charge of the clays. Twenty-five and 50% loading of BTEA cations increased the negative charge on the clay's surface relative to the untreated clay, without affecting the zero point of charge (ZPC) of the clay. Increased QAC loading on HDTMA bentonite causes the surface charge to become more positive and the ZPC increased. One hundred percent of HDTMA bentonite maintained a positive surface charge over the range of pH values tested. The organoclays studied have considerable capacity for heavy metal sorption. Given that prior studies have demonstrated the strong sorption capacity of organoclays for nonionic organic pollutants, it is likely that organoclays can be useful sorbents for the treatment of effluent streams containing both organic contaminants and heavy metals.     

The effect of natural water conditions on the anti-bacterial performance and stability of silver nanoparticles capped with different polymers

This study evaluated the effect of natural water composition onto the bactericidal and physicochemical properties of silver nanoparticles (AgNPs) stabilized with three different polymeric compounds.All the nanoparticles behaved similarly in the water conditions tested. Compared to solutions with low organic matter content and monovalent ions, lower disinfection performances of AgNPs suspensions were obtained in the following order seawater ≤ high organic matter content water ≤ high divalent cations content synthetic water. Suspension of AgNPs in seawater and water with divalent cations (Ca²⁺ and Mg²⁺) formed larger AgNPs aggregates (less than 1400 nm) compared to other solutions tested (up to approximately 38 nm). The critical coagulation concentration (CCC) of AgNPs was determined to quantitatively evaluate the stability of the nanoparticle suspension in different water conditions. When the concentration of dissolved organic matter was increased from 0 mg/L to 5 mg/L, the CCC increased by a factor in the range of 2.19 ± 0.25 for all AgNPs in divalent solutions, but a smaller increase occurred, in the range of 1.54 ± 0.21 fold, when monovalent solutions were used.The concentration of ionic silver released indicated that the dissolved Ag⁺ (3.6-48.2 ppb) was less than 0.5% of the total mass of Ag⁰ added. At all the conditions tested, the concentration of silver ions in solution had a negligible contribution to the overall anti-bacterial performance of AgNPs.This study demonstrated that the anti-bacterial performance of AgNPs at selected natural water conditions decreases in the presence of dissolved natural organic matter or divalent ions, such as humic acid and calcium carbonate. These results may be helpful in understanding the toxicity of AgNP in various natural water conditions and in explaining the risk associated with discharging AgNP in natural aquatic systems.     

Sustainable colloidal-silver-impregnated ceramic filter for point-of-use water treatment

Cylindrical colloidal-silver-impregnated ceramic filters for household (point-of-use) water treatment were manufactured and tested for performance in the laboratory with respect to flow rate and bacteria transport. Filters were manufactured by combining clay-rich soil with water, grog (previously fired clay), and flour, pressing them into cylinders, and firing them at 900 degrees C for 8 h. The pore-size distribution of the resulting ceramic filters was quantified by mercury porosimetry. Colloidal silver was applied to filters in different quantities and ways (dipping and painting). Filters were also tested without any colloidal-silver application. Hydraulic conductivity of the filters was quantified using changing-head permeability tests. [3H]H2O water was used as a conservative tracer to quantify advection velocities and the coefficient of hydrodynamic dispersion. Escherichia coli (E. coli) was used to quantify bacterial transport through the filters. Hydraulic conductivity and pore-size distribution varied with filter composition; hydraulic conductivities were on the order of 10(-5) cm/s and more than 50% of the pores for each filter had diameters ranging from 0.02 to 15 microm. The filters removed between 97.8% and 100% of the applied bacteria; colloidal-silver treatments improved filter performance, presumably by deactivation of bacteria. The quantity of colloidal silver applied per filter was more important to bacteria removal than the method of application. Silver concentrations in effluent filter water were initially greater than 0.1 mg/L, but dropped below this value after 200 min of continuous operation. These results indicate that colloidal-silver-impregnated ceramic filters, which can be made using primarily local materials and labor, show promise as an effective and sustainable point-of-use water treatment technology for the world's poorest communities.