Electro‐Catalytic Degradation of Phenol Organics with SnO2‐Sb2O3/Ti Electrodes

The effect of extraordinary degradation of phenol organics on the SnO₂‐Sb₂O₃/Ti electrode is investigated through experimental research and theoretical analysis. The phenol organics contained 4‐chloro‐phenol, 4‐bromo‐phenol, and 2‐iodo‐phenol. At a current density of 4 mA cm^–2 and an electrolysis time of 12 h, the degradation efficiency of the phenols was over 98% with a relatively short degradation time, whereas the degradation time of the PbO₂/Ti electrode surpassed 40 h while delivering 100% disposal efficiency. Therefore, the effectiveness of electrochemical (EC) oxidation by the SnO₂‐Sb₂O₃/Ti was superior to that of the PbO₂/Ti electrode. At the same time, the SnO₂‐Sb₂O₃/Ti had higher oxygen generation potential and lower electron consumption than the other electrodes. This was mainly due to the effect of the middle Sb₂O₃ layer, which due to its high porosity and good catalytic effect, contributed to a better catalysis than the SnO₂ part.     

Removal of Organic Pollutants from Wastewater Using Wood Fly Ash as a Low‐Cost Sorbent

In this study, untreated and treated wood fly ash (WA) was used as a low‐cost sorbent in batch sorption tests to investigate the removal of organic pollutants from a real wastewater generated by cleaning/washing of machinery in a wood‐laminate floor industry in Sweden. The experiments focused on the effect of the WA dosage and particle size on the removal efficiency for organic compounds. With a WA dosage of 160 g L^?1 and a particle size less than 1 mm, the reductions of chemical oxygen demand (COD), biologic oxygen demand, and total organic carbon were 37 ± 0.4, 24 ± 0.4, and 30 ± 0.3%, respectively. Pre‐treatment of WA with hot water improved the COD removal efficiency by absorption from 37 ± 0.4 to 42 ± 1.6% when the same dosage (160 g L^?1) was applied. Sorption isotherm and sorption kinetics for COD using untreated WA can be explained by Freundlich isotherm and pseudo‐second‐order kinetic models. Intra‐particle diffusion model indicates that pore diffusion is not the rate‐limiting step for COD removal. Based on the experimental data, WA could be used as an alternative low‐cost sorption media/filter for removal of organic compounds from real industrial wastewater.     

Evaluation of Two Low‐Cost–High‐Performance Adsorbent Materials in the Waste‐to‐Product Approach for the Removal of Pesticides from Drinking Water

This study evaluates the performance of two low cost and high performance adsorption materials, i.e., activated carbon produced from two natural waste products: Bamboo and coconut shell, in the removal of three pesticides from drinking water sources. Due to the fact that bamboo and coconut shell are abundant and inexpensive materials in many parts of the world, they respond to the “low‐cost” aspect. The adsorption capacities of two local adsorbents have been compared with commercial activated carbon to explore their potential to respond to the “high quality” aspect. Two pesticides were selected, namely dieldrin and chlorpyrifos, because they are commonly used in agriculture activities, and may remain in high concentrations in surface water used as drinking water sources. The results indicate that the adsorption of pesticides on activated carbons is influenced by physico‐chemical properties of the activated carbon and the pesticides such as the presence of an aromatic ring, and their molar mass. The activated carbon produced from bamboo can be employed as low‐cost and high performance adsorbent, alternative to commercial activated carbon for the removal of pesticides during drinking water production. The performance of activated carbon from bamboo was better due to its relatively large macroporosity and planar surface. The effect of adsorbent and pesticide characteristics on the performance was derived from batch experiments in which the adsorption behavior was studied on the basis of Freundlich isotherms.     

Vertical seismic profiling using a daisy‐chained deployment of fibre‐optic cables in four wells simultaneously – Case study at the Ketzin carbon dioxide storage site

The geological storage of carbon dioxide is considered as one of the measures to reduce greenhouse gas emissions and to mitigate global warming. Operators of storage sites are required to demonstrate safe containment and stable behaviour of the storage complex that is achieved by geophysical and geochemical monitoring, combined with reservoir simulations. For site characterization, as well as for imaging the carbon dioxide plume in the reservoir complex and detecting potential leakage, surface and surface‐borehole time‐lapse seismic monitoring surveys are the most widespread and established tools. At the Ketzin pilot site for carbon dioxide storage, permanently installed fibre‐optic cables, initially deployed for distributed temperature sensing, were used as seismic receiver arrays, demonstrating their ability to provide high‐resolution images of the storage formation. A vertical seismic profiling experiment was acquired using 23 source point locations and the daisy‐chained deployment of a fibre‐optic cable in four wells as a receiver array. The data were used to generate a 3D vertical seismic profiling cube, complementing the large‐scale 3D surface seismic measurements by a high resolution image of the reservoir close to the injection well. Stacking long vibro‐sweeps at each source location resulted in vertical seismic profiling shot gathers characterized by a signal‐to‐noise ratio similar to gathers acquired using geophones. A detailed data analysis shows strong dependency of data quality on borehole conditions with significantly better signal‐to‐noise ratio in regions with good coupling conditions.     

Fate of Benzalkonium Chloride in a Sewage Sludge Low Temperature Conversion Process Investigated by LC‐LC/ESI‐MS/MS

Thermocatalytic low temperature conversion (LTC) is a new method for the disposal of sewage sludge. Using this method, sludge is converted into a residual solid (coal) along with reaction water, oil, and non‐condensable gases. The oil can be used as an energy source and the coal as a substitute for charcoal. To this end, it is important to determine whether there are any easily available contaminants present in the coal generated by the process. Contaminants that can be strongly sorbed by sewage sludge solids are, e. g., pharmaceuticals and disinfectants. As an example the fate of the persistent and strong adsorbing disinfectant benzalkonium chloride (BAC) has been investigated within the LTC process. The sewage sludge was spiked with BAC and then subjected to the LTC process. The resulting coal was extracted and analyzed using LC‐LC/ESI‐MS/MS (ion trap). BAC could not be detected in the LTC coal, although it could be extracted from the spiked sludge before the LTC treatment. It can thus be concluded that the investigated compound is not easily available in the coal, and hence that its use does not present a risk.     

CO2 Degassing over Seismic Areas: The Role of Mechanochemical Production at the Study Case of Central Apennines

Field observations coupled with experimental results show that CO₂ can be produced by mechanical energy applied to carbonate rocks becoming an unexpected additional gas source besides that degassed from the mantle or produced by thermometamorphism. The evidence that a large amount of carbon dioxide associated with radiogenic-type helium (R/Ra as low as 0.01–0.08) is released through continental areas, denotes the absence of a contribution from the mantle or from mantle-derived fluids. Data collected during the seismic crisis which struck the Central Apennines in 1997–98 have shown an enhanced CO₂ flux not associated with the presence of mantle or thermometamorphic-derived fluids. On the other hand, new experimental results highlight the possibility of producing CO₂ by mechanical energy that acts on the calcite crystalline lattice. While the CO₂ released over the geothermal areas (e.g., Larderello Geothermal Field) is obviously derived by mantle-derived activities, this is not the case of the huge amount of CO₂ released over the seismically active areas where the presence mantle-derived products is ruled out. We propose that mechanical energy, e.g., released during seismic events, microseismicity or creeping processes is a possible additional energy source able to produce CO₂ and thus could explain the presence of CO₂ degassing over tectonic areas where the influence of the mantle is low.     

Temperature‐Activated Auto‐Decomposition Reactions: An Under‐Utilized In Situ Remediation Solution

The remediation industry has witnessed multiple innovations arising from a greater understanding of the physical, chemical, and biological processes that control the fate and transport of chemicals in the subsurface environment. In addition, increasing emphasis is being placed on remediation solutions that are greener, simpler, and more resource efficient. The positive impacts that can be derived from this emphasis include reduced energy consumption, reduced waste emissions, and lower costs. Temperature‐activated auto‐decomposition reactions represent a potentially underutilized option for the in situ remediation of certain organic contaminants, and an option that can be both highly effective and greener than other available technologies.     

Metal Impregnated Silica‐Carbon Materials from Rice Husk: A Versatile Sorbent for Toxic Organics and Inorganics in Water and Air

Carbon bearing materials derived from rice husk (RH) have long been recognized as sorbents for diverse chemicals – both organic and inorganic. This work presents an overview of studies demonstrating a single step process of carbonization of chemically pretreated RH to produce metal impregnated silica‐carbon char designated as silicarbon materials that can be utilized in sorbing out water‐borne organic and inorganic hazardous substances (such as phenol, hexavalent chromium, fluoride, and arsenic) and air‐borne volatile organic chemicals (such as acetone, chloroform, benzene, and pyridine). The metal‐impregnated silicarbon solids derived from RH appear to constitute renewable, low‐cost, user‐friendly, and efficient materials for control systems for indoor air contamination and for industrial as well as non‐industrial hazardous aqueous pollution.     

Characterization and Source History Modeling Using Low‐k Zone Profiles at Two Source Areas

Like tree rings, high‐resolution soil sampling of low‐permeability (low‐k) zones can be used to evaluate the style of source history at contaminated sites (i.e., historical pattern of concentration and composition vs. time since releases occurred at the interface with the low‐k zone). This is valuable for the development of conceptual site model (CSM) and can serve as an important line of evidence supporting monitored natural attenuation (MNA) as a long‐term remedy. Source histories were successfully reconstructed at two sites at Naval Air Station Jacksonville using a simple one‐dimensional (1D) model. The plume arrival time and historical composition were reconstructed from the time initial releases that were suspected to occur decades earlier. At the first site (Building 106), the source reconstructions showed relatively constant source concentrations, but significant attenuation over time in the downgradient plume in the transmissive zone, suggesting MNA may not be an appropriate remedy if source control is a requirement, but attenuation processes are clearly helping to maintain plume stability and reduce risk. At the second site (Building 780), source concentrations in the transmissive zone showed an approximately a one order of magnitude over time, but apparently less attenuation in the downgradient plume. The source reconstruction method appeared to reflect site remediation efforts (excavation, soil vapor extraction) implemented in the 1990s. Finally, a detailed analysis using molecular biological tools, carbon isotopes, and by‐products suggests that most degradation activity is associated with high‐k zones but not with low‐k zones at these source areas. Overall, the source reconstruction methodology provided insight into historical concentration trends not obtainable otherwise given the limited long‐term monitoring data.     

Degradation of Phenol in Aqueous Solution by Fenton,Sono‐Fenton and Sono‐photo‐Fenton Methods

The present work focuses on the performance of Fenton, sono‐Fenton, and sono‐photo‐Fenton processes for the oxidation of phenol present in aqueous solution. The effects of H₂O₂ concentration, Fe²⁺ concentration, pH, and initial phenol concentration on the oxidation of phenol were studied. The optimum Fe²⁺ and H₂O₂ concentrations for the Fenton process were 45 and 800 mg/L, respectively. For the sono‐Fenton process, the optimum Fe²⁺ and H₂O₂ concentrations were 30 and 800 mg/L, respectively. The optimal conditions for the sono‐photo‐Fenton process were found to be 20 mg/L of Fe²⁺ and 700 mg/L of H₂O₂. The optimum pH was found to be 3 for the processes investigated in the present study. The analysis of results showed that the sono‐photo‐Fenton method reduced the Fe²⁺ concentration by 30–50% and the H₂O₂ concentration by 12.5%. It was found that the sono‐photo‐Fenton technique showed better performance than the Fenton and sono‐Fenton processes for the oxidation of phenol. A lumped kinetic model was used to predict the chemical oxygen demand reduction and the model was found to fit the data.     

Response Surface Modeling and Optimization of Microwave‐Activated Persulfate Oxidation of Olive Oil Mill Wastewater

Olive oil mill wastewater (OMW) is environmentally hazardous not only because it contains high recalcitrant and toxic compounds, but also due to its high organic load and turbidity. In this study, oxidation of OMW by microwave (MW)‐activated persulfate is investigated. Box–Behnken design is applied to investigate the effects of operating conditions on operating cost, organic matter, and color removal. Multi response optimization is performed according to minimum operating cost, maximum organic matter and color removal efficiencies. At optimum conditions (persulfate anion dose of 266 g L^?1, oxidation duration of 23.58 min, MW power of 567 W, and initial pH 2), chemical oxygen demand (COD) removal of 63.38%, color removal of 94.85%, and operating cost of 0.0633 Euro/g total organic carbon (TOC) removal are found. The biochemical oxygen demand (BOD₅)/COD ratio is increased from 0.144 to 0.285. Results of Pareto analysis show individual effect of MW power is 92.81% for TOC removal, 15.52% for color removal, 68.99% for operating cost, respectively. According to the results, it is not recommended to use this process as an ultimate treatment unit due to the high amount of oxidizing agent consumed. Instead, it is recommended to be used as a pre‐ or post‐treatment step.     

Freeze Shoe Sampler for the Collection of Hyporheic Zone Sediments and Porewater

The Starr and Ingleton (1992) drive point piston sampler (DPPS) design was modified by fitting it with a Murphy and Herkelrath (1996) type sample‐freezing drive shoe (SFDS), which uses liquid carbon dioxide as a cryogen. Liquid carbon dioxide was used to freeze sediments in the lower 0.1 m of the core and the drive‐point piston sealed the core at the top preserving the reductive‐oxidation (redox) sensitive sediments from the atmosphere and maintaining natural stratigraphy. The use of nitrogen gas to provide positive pressure on the gas system blocked the ingress of water which froze on contact with the cryogen thus blocking the gas lines with ice. With this adaptation to the gas system cores could be collected at greater depths beneath the static water level. This tool was used to collect intact saturated sediment cores from the hyporheic zone of the tidally influenced Fraser River in Vancouver, British Columbia, Canada where steep geochemical and microbial gradients develop within the interface between discharging anaerobic groundwater and recharging aerobic river water. In total, 25 cores driven through a 1.5 m sampling interval were collected from the river bed with a mean core recovery of 75%. The ability to deploy this method from a fishing vessel makes the tool more cost effective than traditional marine‐based drilling operations which often use barges, tug boats, and drilling rigs.     

Comparison of migration‐based location and detection methods for microseismic events

Microseismic monitoring in the oil and gas industry commonly uses migration‐based methods to locate very weak microseismic events. The objective of this study is to compare the most popular migration‐based methods on a synthetic dataset that simulates a strike‐slip source mechanism event with a low signal‐to‐noise ratio recorded by surface receivers (vertical components). The results show the significance of accounting for the known source mechanism in the event detection and location procedures. For detection and location without such a correction, the ability to detect weak events is reduced. We show both numerically and theoretically that neglecting the source mechanism by using only absolute values of the amplitudes reduces noise suppression during stacking and, consequently, limits the possibility to retrieve weak microseismic events. On the other hand, even a simple correction to the data polarization used with otherwise ineffective methods can significantly improve detections and locations. A simple stacking of the data with a polarization correction provided clear event detection and location, but even better results were obtained for those data combined with methods that are based on semblance and cross‐correlation.     

Semi‐Micro Reflux Procedure for Minimization of Chloride Interference by COD Determination

In this study, a semi‐micro procedure for the COD (Chemical Oxygen Demand) was undertaken to allow the measurement of effluent samples with a high chloride content. It was found that the COD values for standard and effluent samples, corresponded closely to those obtained using the standard method of Burns and Marshall. When the method was applied to samples of industrial wastewater, with a very high chloride content, the recommended procedure proved to be accurate and precise, with RSDs of 6% and 4.3% for the standard and effluent solutions, respectively. The required amount of hazardous reagents was similar to that found in the standard closed reflux method. It was also possible to determine the total amount of oxidized halides. The use of this low‐cost, laboratory‐made system made it unnecessary to acquire an expensive, imported analytical system, while maintaining a high level of accuracy in the determinations.     

Arsenic — a Review. Part II: Oxidation of Arsenic and its Removal in Water Treatment

In natural waters arsenic normally occurs in the oxidation states +III (arsenite) and +V (arsenate). The removal of As(III) is more difficult than the removal of As(V). Therefore, As(III) has to be oxidized to As(V) prior to its removal. The oxidation in the presence of air or pure oxygen is slow. The oxidation rate can be increased by ozone, chlorine, hypochlorite, chlorine dioxide, or H₂O₂. The oxidation of As(III) is also possible in the presence of manganese oxide coated sands or by advanced oxidation processes. Arsenic can be removed from waters by coprecipitation with Fe(OH)₃, MnO₂ or during water softening. Fixed‐bed filters have successfully been applied for the removal of arsenic.The effectiveness of arsenic removal was tested in the presence of adsorbents such as FeOOH, activated alumina, ferruginous manganese ore, granular activated carbon, or natural zeolites. Other removal technologies are anion exchange, electrocoagulation, and membrane filtration by ultrafiltration, nanofiltration or reverse osmosis.     

Sedimentary and geochemical characterization of Middle–Late Miocene formations in the Neogene Tsugaru Basin,Japan by means of DTH27‐1 well sediment analysis

Middle–Late Miocene age siliceous formations outcropping along the northwestern side of Honshu Island are considered prospective source rocks for hydrocarbons. An analysis of geophysical, sedimentological, and geochemical properties is essential to evaluate the formations' source potential, and to understand the factors that determined the accumulation and preservation of organic matter. This study investigates the Middle–Late Miocene geological record of the Tsugaru back‐arc basin, located in the western part of Aomori prefecture, through an analysis of a 200 m long portion of a core from the DTH27‐1 well; this core is composed of the diatomaceous siltstones of the Akaishi Formation and the siliceous mudstones of the Odoji Formation. Sedimentological and geophysical characterization showed that the Akaishi Formation's diatomaceous siltstones are mostly massive and bioturbated, have low magnetic susceptibility, and demonstrate moderate natural radioactivity. Although the Odoji Formation's siliceous mudstones are massive, they have exceedingly low magnetic susceptibility and high natural radioactivity. Geochemical data from a Rock‐Eval Pyrolysis such as total organic carbon and generative potential (S1 + S2) revealed that, in the Tsugaru area, only the Odoji Formation is a likely prospective source rock for hydrocarbons. On the other hand, T_max values indicate that both the formations are thermally immature for generating hydrocarbons. The difference between the Akaishi and Odoji Formation in the sedimentological facies, in terms of the degree of bioturbation and the organic carbon content, indicates variations in lithological properties, such as porosity and grain size; moreover, this difference indicates a variation in the paleo‐oxygenation of bottom waters, with the transition from oxygen‐deficient conditions in the Middle Miocene to the more oxygenated conditions in the Late Miocene. Both the lithological and paleo‐environmental factors possibly influenced the organic richness in the two formations.     

Development of Bench‐Scale Bio‐Packed Column for Wastewater Treatment from Optical Emission Spectrometry

An eco‐friendly and inexpensive technique for wastewater treatment originated from inductively coupled plasma‐optical emission spectrometry (ICP‐OES) is presented within this paper. The proposed process comprised of loading waste crab shells in packed column for adsorption of heavy metal ions, followed by desorption using 0.01 M HCl. An exhaustive physical and chemical characterization of ICP‐OES wastewater revealed the complex nature of effluent, including the presence of 15 different metals and metalloid under strong acidic condition (pH 1.3). Based on the preliminary batch experiments, it was identified that solution pH played a major role in metal sequestration by crab shell with pH 3.5 identified as optimum pH. Rapid metal biosorption kinetics along with complete desorption and subsequent reuse for three cycles was possible with crab shell‐based treatment process. Continuous flow‐through column experiments confirmed the high performance of crab shell towards multiple metal ions with the column able to operate for 22 h at a flow rate of 10 mL/min before outlet concentration of arsenic reached 0.25 times of its inlet concentration. Other metal ions such as Cu, Cd, Co, Cr, Pb, Ni, Zn, Mn, Al, and Fe were only in trace levels in the treated water until 22 h. The performance of the treatment process was compared with trade effluent discharge standards, and the process flow diagram along with cost analysis was suggested.     

Quasi‐static and pseudo‐dynamic testing of unbonded post‐tensioned rocking bridge piers with external replaceable dissipaters

It has been well documented that following a major earthquake a substantial percentage of economic loss results from downtime of essential lifelines in and out of major urban centres. This has thus led to an improvement of both performance‐based seismic design philosophies and to the development of cost‐effective seismic structural systems capable of guaranteeing a high level of protection, low structural damage and reduced downtime after a design‐level seismic event. An example of such technology is the development of unbonded post‐tensioned techniques in combination with rocking–dissipating connections. In this contribution, further advances in the development of high‐performance seismic‐resistant bridge piers are achieved through the experimental validation of unbonded post‐tensioned bridge piers with external, fully replaceable, mild steel hysteretic dissipaters. The experimental response of three 1 : 3 scale unbonded, post‐tensioned cantilever bridge piers, subjected to quasi‐static and pseudo‐dynamic loading protocols, are presented and compared with an equivalently reinforced monolithic benchmark. Minimal physical damage is observed for the post‐tensioned systems, which exhibit very stable energy dissipation and re‐centring properties. Furthermore, the external dissipaters can be easily replaced if severely damaged under a major (higher than expected) earthquake event. Thus, negligible residual deformations, limited repair costs and downtime can be achieved for critical lifeline components. Satisfactory analytical–experimental comparisons are also presented as a further confirmation of the reliability of the design procedure and of the modelling techniques. Copyright © 2008 John Wiley & Sons, Ltd.     

Robotic photosieving from low‐cost multirotor sUAS: a proof‐of‐concept

Measurement of riverbed material grain sizes is now a routine part of fieldwork in fluvial geomorphology and lotic ecology. In the last decade, several authors have proposed remote sensing approaches of grain size measurements based on terrestrial and aerial imagery. Given the current rise of small unmanned aerial system (sUAS) applications in geomorphology, there is now increasing interest in the application of these remotely sensed grain size mapping methods to sUAS imagery. However, success in this area has been limited owing to two fundamental problems: lack of constraint of image scale for sUAS imagery and blurring effects in sUAS images and resulting orthomosaics. In this work, we solve the former by showing that SfM‐photogrammetry can be used in a direct georeferencing (DG) workflow (i.e. with no ground validation) in order to predict image scale within margins of 3%. We then propose a novel approach of robotic photosieving of dry exposed riverbed grains that relies on near‐ground images acquired from a low‐cost sUAS and which does not require the presence of ground control points or visible scale objects. We demonstrate that this absence of scale objects does not affect photosieving outputs thus resulting in a low‐cost and efficient sampling method for surficial grains. Copyright © 2017 John Wiley & Sons, Ltd.     

Electro‐Fenton Treatment of Photographic Processing Wastewater

In this work, the treatment of photographic processing wastewaters (PPW) by electro‐Fenton process has been investigated. The Influence of operating conditions on kinetics and efficiency of electro‐Fenton process has been evaluated using carbon felt cathode and platinium (Pt) or boron‐doped diamond (BDD) anode. The results of electro‐Fenton treatment of PPW have shown that nearly complete removal of total phenols was obtained for all combinations with pseudo‐first rate constants of 0.07, 0.012, and 0.018/min for carbon felt/Pt, carbon felt/BDD and Pt/BDD cathode/anode combinations, respectively. The combination of carbon felt cathode with BDD anode achieved the highest total organic carbon (TOC) removal of 90%, while it did not exeed 40% for carbon felt/Pt combination. Increasing current intensity and Fe²⁺ dose enhances the efficiency of electro‐Fenton process. However, increasing pH decreases TOC removal during the treatment of PPW by electro‐Fenton process. The highest efficiency of electro‐Fenton process using BDD anode can be explained by the contribution of direct and indirect oxidation routes in the degradation mechanism of organics including (i) oxidation via hydroxyl radicals generated from the catalytic decomposition of H₂O₂ and from water discharge on BDD anode, (ii) direct oxidation of certain organic compounds on BDD anode, and (iii) mediated oxidation with inorganic oxidants electrogenerated from anodic oxidation of supporting salts.