Passive air samplers (PAS) using XAD-resin were deployed at a wide variety of sites around the world for four years to asses the spatial and temporal trends of legacy organochlorine pesticides (OCPs) and current use pesticides (CUPs) in the global atmosphere. Legacy OCPs are prevalent in developing countries, whereas certain CUPs dominate in North America and Europe. OCP levels are declining world wide. Concentrations from the XAD-based PAS agreed with those from polyurethane foam (PUF) disk PAS within a factor of 4 for most sites. The comparison revealed that the sampling rate of the PUF-based PAS is more dependent on wind speed, whereas that of the XAD-PAS has a higher dependence on temperature. Analysis of PAS deployed across arid, subtropical Botswana showed that recent use has more impact on present day air concentrations than historical use. Year-long measurements by high volume air sampling in Botswana yielded higher HCB levels in winter, and higher endosulfan levels in summer. Those variations are neither related to temperature fluctuation nor seasonal hydrological events, and are therefore more likely caused by pesticide usage pattern. Very low levels of OCPs were found in the warm, dry, low organic matter soils of Botswana, including in soils from historical use areas. Such soils appear to have a low long-term storage capacity for pesticides allowing for rapid volatilization. They are thus not long-term sources of pesticides to the atmosphere. Endosulfan sulfate levels were observed to increase in tropical soils with increasing elevation. Water samples from high altitude cloud forests in Costa Rica contained very low concentrations of CUPs and it is unlikely that that those levels pose a threat to amphibians in cloud forests. Laboratory experiments and literature analysis showed that the inert gas stripping method for the determination of air-water partitioning equilibria is susceptible to surface sorption artifacts for chemicals with a interface-air partition coefficient log (KIA/m) > -3. Using larger bubbles reduces the surface-to-volume ratio and produces accurate air-water partition coefficients for chemicals with log (KIA/m) < -1.2.

Passive air samplers (PAS) using XAD-resin were deployed at a wide variety of sites around the world for four years to asses the spatial and temporal trends of legacy organochlorine pesticides (OCPs) and current use pesticides (CUPs) in the global atmosphere. Legacy OCPs are prevalent in developing countries, whereas certain CUPs dominate in North America and Europe. OCP levels are declining world wide. Concentrations from the XAD-based PAS agreed with those from polyurethane foam (PUF) disk PAS within a factor of 4 for most sites. The comparison revealed that the sampling rate of the PUF-based PAS is more dependent on wind speed, whereas that of the XAD-PAS has a higher dependence on temperature. Analysis of PAS deployed across arid, subtropical Botswana showed that recent use has more impact on present day air concentrations than historical use. Year-long measurements by high volume air sampling in Botswana yielded higher HCB levels in winter, and higher endosulfan levels in summer. Those variations are neither related to temperature fluctuation nor seasonal hydrological events, and are therefore more likely caused by pesticide usage pattern. Very low levels of OCPs were found in the warm, dry, low organic matter soils of Botswana, including in soils from historical use areas. Such soils appear to have a low long-term storage capacity for pesticides allowing for rapid volatilization. They are thus not long-term sources of pesticides to the atmosphere. Endosulfan sulfate levels were observed to increase in tropical soils with increasing elevation. Water samples from high altitude cloud forests in Costa Rica contained very low concentrations of CUPs and it is unlikely that that those levels pose a threat to amphibians in cloud forests. Laboratory experiments and literature analysis showed that the inert gas stripping method for the determination of air-water partitioning equilibria is susceptible to surface sorption artifacts for chemicals with a interface-air partition coefficient log (KIA/m) > -3. Using larger bubbles reduces the surface-to-volume ratio and produces accurate air-water partition coefficients for chemicals with log (KIA/m) < -1.2.

In Sweden more than 400 000 private households have not yet sufficient wastewater purification. These effluent is considered as an increasing problem and many onsite purification methods have been studied. In this investigation, the method of reactive bed filters have been tested by column and batch experiments. Five different kinds of filter materials with reactive surfaces have been studied concerning their capacity to absorb ammonium and phosphorus from wastewater. The materials that were examined are Filtra N, wollastonite Filtra P, blast furnace slag and Polonite®. The first two materials were examined for their capacity to remove ammonium, and the others for their phosphorus removal capacity. Ten columns were used, two for each material. A synthetic solution with the ammonium and phosphate concentration similar to that of domestic wastewater (NH4-N 30 mg/l; PO4-P 5 mg/l) were pumped to the columns under two flow regimes. Five columns were continuously saturated with solution and the other five columns were saturated under three one hour periods a day The solution was pumped three times a day to the columns at a volume equal to the pore volume of each material. The objective of the batch experiment was to find out how variations in pH-value and concentration of the nutrients influenced the sorption capacity of the materials. The result was then used for modelling in the computer program Visual Minteq to determine the probability of precipitation of known compounds. Results from the column experiment showed that sorption of phosphorus in both saturated columns and intermittently saturated columns were 96 % or more for blast furnace slag, Filtra P and Polonite®. Filtra N showed the best ammonium sorption with 92 %. Sorption of ammonium was much better in periodically saturated columns for the material wollastonite. The wollastonite used in this experiment showed a higher phosphorus sorption capacity than expected. A possible explanation could be that the easy weathering of Ca-silicate compounds favoured the sorption of phosphorus. Results from Visual Minteq modelling showed that the probability of calcite formation in Filtra P and Polonite® are very likely. The two materials had high pH-values and the calcite was most likely formed at values of pH &gt; 10. Hydroxyapatite is the most common precipitation when phosphorus sorption occurs and is suggested to be formed in wollastonite. / Mer än hälften av Sveriges enskilda avlopp bedöms inte uppfylla kraven i miljöbalken på längre gående rening än slamavskiljning. Dessa står för en betydande del av fosfor- och kväveutsläppen till hav, sjöar och vattendrag. Åtskilliga systemlösningar utreds, men i denna rapport har filter med fosfor- och kvävesorberande förmågor testats eller s.k. reaktiva filter. Mineraliska filter som ingått i studien är Filtra N, wollastonit, Filtra P, hyttsand och Polonite®. De två första filtren studerades speciellt på deras förmåga att avskilja ammonium och de tre övriga främst på deras fosforavskiljnings förmåga. Kolonnförsök utfördes med tio kolonner där fem belastades med mättat flöde och de övriga med intermittent mättat flöde. Kolonnuppsättningen var två kolonner per filtermaterial med vardera olika flödesförhållanden. Belastningen på kolonnerna sattes till betydligt högre än traditionell infiltration/markbädd. Ett artificiellt avloppsvatten användes och tillreddes med en koncentration av kväve (NH4-N) på 30 mg/l och fosforkoncentration (PO4-P) på 5 mg/l. De valda koncentrationerna efterliknar ett vanligt hushållsspillvatten. Skakförsök utfördes för att undersöka sorptionsförmågan hos de olika mineraliska filtren där vikten låg på hur koncentrationen av näringsämnena och pH påverkar sorptionen. Resultaten från skakförsöken utvärderades med jämviktsmodellen Visual Minteq. Sannolikheten att kända utfällningar bildas studerades. Resultaten från kolonnförsöken visade att hyttsand, Filtra P och Polonite® gav bäst fosforavskiljning med över 96 % för båda flödesregimerna. Filtra N var den bästa ammoniumavskiljaren med över 92 %. Wollastonit hade en bättre avskiljning med intermittent mättat flöde med 65 % jämfört med 11 % för mättat flöde. En intressant iakttagelse var att wollastonit hade en bättre fosforavskiljning än ammoniumavskiljning med ca 60 % för båda flödena. Det kan bero på att filtret innehåller lättvittrade Ca-silikatföreningar som ökar fosfatavskiljningen. Skakförsöken resulterade i att för Filtra P, hyttsand och Polonite® sorberades all tillsatt fosfat. Filtra N visade samma resultat som i kolonnförsöken med över 92 % sorption. Endast fosfat sorberades vid försök med tillsättning av både fosfat och ammonium till hyttsand och wollastonit. Vid modellering i Visual Minteq finns det en viss sannolikhet att kalcit bildats i Filtra P och Polonite® p g a deras höga pH, kalcit fälls ut vid pH &gt; 10. Hydroxyapatit som är den vanligaste utfällningen av kalciumfosfat vid avskiljning av fosfor bildades mycket troligt i wollastonit.

No description available.

Zeolite beta has been synthesized using hydrothermal methods. In order to synthesize zeolite beta an aqueous gel having a molar batch composition of 2.2 Na2O&amp / #8729 / Al2O3&amp / #8729 / x SiO2&amp / #8729 / 4.6 (TEA)2O&amp / #8729 / 444 H2O was utilized. The synthesis parameters were SiO2/Al2O3 ratio (20 &amp / #8804 / x &amp / #8804 / 50) and crystallization time (6 &amp / #8804 / t &amp / #8804 / 16 days). Pure zeolite beta was crystallized from the experiments which were performed with the batch composition having SiO2/Al2O3 of 20 and 30 in 6 to 16 days period. For SiO2/Al2O3 of 20 and 30, the highest yield was obtained for 12 days. Therefore, the rest of the experiments, in which SiO2/Al2O3 was 40 and 50, were carried out keeping the synthesis time constant (12 days). Pure zeolite beta was also synthesized for SiO2/Al2O3 of 40 and 50. The highest yield and the most crystalline zeolite beta sample were obtained from the experiment performed at SiO2/Al2O3 of 50 with a synthesis time of 12 days. The morphology and crystal size of the zeolite beta samples were identified by using scanning electron microscope (SEM). It was observed that, zeolite beta samples had spheroidal morphology with the crystal size of about 0.5 &amp / #956 / m. According to the thermogravimetric analyses (TGA), it was found that template molecules and moisture constituted nearly 18 % by weight of the zeolite beta samples. The surface area of the calcined zeolite beta sample was determined by N2 adsorption and was found to be 488 m2/g. Gravimetric sorption analyses yield that, the limiting sorption capacity of Na-Beta for methanol, ethanol, isopropanol and n-butanol at 0&deg / C was about the same with a value of 0.25 cm3/g. For o-xylene, m-xylene and p-xylene that value was 0.21 cm3/g, 0.22 cm3/g and 0.24 cm3/g, respectively.

To achieve predictive capability for complex environmental systems with coagulation and arsenic sorption, a unified improved coagulation model coupled with arsenic sorption was developed. A unified coagulation model coupled with arsenic sorption was achieved by the following steps: (1) an improved discretized population balance equation (PBE) was developed to obtain the exact solution of conventional coagulation, (2) the improved PBE was extended to an adjustable geometric size interval having higher numerical stability, accuracy, and computational efficiency than existing models for fractal aggregate coagulation that includes agglomeration and fragmentation, (3) a surface complexation equilibrium model and a sorption kinetic model was introduced to predict arsenic sorption behavior onto hydrous metal oxide surfaces, and (4) an improved discretized PBE was coupled with arsenic sorption kinetics and equilibrium models by aid of collision efficiency ?? depending on surface charge (potential) on the hydrous metal oxide particles, colliding particle size ratio, and fluid strain-rate in applied flow system. The collision efficiency ?? into the improved (r,r)ij(r,r)ijdiscretized coagulation model for fractal aggregate yielded a unified improved coagulation model coupled with arsenic sorption kinetics and the equilibrium model. Thus, an improved unified coagulation model could provide high statistical accuracy, numerical stability, and computational efficiency to enhance predictive capability for behavior of arsenic sorption and fractal colloid particle aggregation and break-up, simultaneously. From the investigation, it is anticipated that the unified coagulation model coupled with arsenic sorption kinetics and equilibrium will provide a more complete understanding of the arsenic removal mechanism and its application to water/wastewater treatment. Further, this coupled model can be applied to other water and wastewater treatment systems combined with sorption and filtration processes. These combined processes can be optimized by the coupled model that was developed in this study. By simulating the arsenic sorption and particle size distribution as a pretreatment before filtration (sand filtration or membrane filtration), the overall arsenic removal efficiency and operation cost can be estimated.

RES³T - the Rossendorf Expert System for Surface and Sorption Thermodynamics - is a digitized thermodynamic sorption database, implemented as a relational database. It is mineral-specific and can therefore also be used for additive models of more complex solid phases such as rocks or soils. An integrated user interface helps users to access selected mineral and sorption data, to extract internally consistent data sets for sorption modeling, and to export them into formats suitable for other modeling software. Data records comprise of mineral properties, specific surface area values, characteristics of surface binding sites and their protolysis, sorption ligand information, and surface complexation reactions. An extensive bibliography is also included, providing links not only to the above listed data items, but also to background information concerning surface complexation model theories, surface species evidence, and sorption experiment techniques. The RES³T database is intended for an international use. This requires high standards in availability, consistency and actuality. Therefore the authors of the database decided to couple the database onto an authorization tool.

Pharmaceuticals, personal care products and dissolved organic matter (OM) are introduced to soil via irrigation with reclaimed wastewater. This thesis examines the basic factors that influence sorption of these components in soil. Sorption of dissolved OM samples of varying composition to clay surfaces was examined. Results indicate that preferential sorption is dependent on clay type but not necessarily OM composition. Analysis of soils revealed aliphatic components, carbohydrates and amino acids are prevalent at the soil-water interface whereas aromatics are inaccessible at the soil-water interface. No clear relationship between sorption affinity of 17β-estradiol, sulfamethoxazole, carbamazepine and phenanthrene and soil OM aromaticity or aliphaticity was observed. A negative relationship between sorption and O-alkyl content may be due to these components blocking contaminant access to high affinity sorption sites. Therefore, application of reclaimed wastewater to soils with O-alkyl-rich OM may result in higher mobility of contaminants.

Pharmaceuticals, personal care products and dissolved organic matter (OM) are introduced to soil via irrigation with reclaimed wastewater. This thesis examines the basic factors that influence sorption of these components in soil. Sorption of dissolved OM samples of varying composition to clay surfaces was examined. Results indicate that preferential sorption is dependent on clay type but not necessarily OM composition. Analysis of soils revealed aliphatic components, carbohydrates and amino acids are prevalent at the soil-water interface whereas aromatics are inaccessible at the soil-water interface. No clear relationship between sorption affinity of 17β-estradiol, sulfamethoxazole, carbamazepine and phenanthrene and soil OM aromaticity or aliphaticity was observed. A negative relationship between sorption and O-alkyl content may be due to these components blocking contaminant access to high affinity sorption sites. Therefore, application of reclaimed wastewater to soils with O-alkyl-rich OM may result in higher mobility of contaminants.

Solidification/Stabilization (S/S) is a low cost remedial technology that is being used with success to remediate sites that contain higher molecular weight organic compounds, leading to a need to research the interaction of organic contaminants with cement-based S/S materials. The objective of this study was to examine the sorption levels of naphthalene to cement-based S/S materials. Batch testing was performed with S/S materials containing different amounts of organic carbon to investigate the sorption of naphthalene. It was found that sorption values varied, but appear to be dependent on the organic carbon present. Dynamic leach test (ANS16.1 methodology) and SPLP analysis results are presented for intact cement-based S/S materials. Contaminant migration modeling was performed to use the information obtained in the study to compare the sorption capacity of cement-based S/S systems. It was shown that cement-based S/S remediation systems can provide long-term protection against naphthalene contaminant migration.