Novel mesoporous microspheres of Al and Ni doped LMO spinels and their performance as cathodes in secondary lithium ion batteries

A facile, scalable, and solution-based technique is used to fabricate Al and Ni-doped (LiAl_0.1Mn_1.9O₄ and LiAl_0.1Ni_0.1Mn_1.8O₄) microspheres of lithium manganese oxide (LMO) spinels for use as reversible cathode materials for lithium ion batteries (LIBs). The spheres of the two samples exhibit different porosities. Cells with these LMO-based cathodes are then cycled between 4.5 V and 2 V to study their stabilities while simultaneously being subjected to the undesirable Jahn-Teller distortion that occurs around the ~3 V regime. The LiAl_0.1Mn_1.9O₄ (LAMO) and the LiAl_0.1Ni_0.1Mn_1.8O₄ (LANMO) cells exhibit comparable open circuit voltages (OCV) of 2.94 V and 2.97 V, respectively. During cell cycling, the LAMO cell exhibits a maximum specific capacity of 122.51 mAh g^?1 with a capacity fade of 65.35% after 75 cycles. The LiAl_0.1Ni_0.1Mn_1.8O₄ (LAMO) sample fares better and exhibits a maximum of 140.49 mAh g^?1 and a capacity drop of 52.59%. Detailed structural studies indicate that Ni doping and the greater degree of porosity of the LANMO sample to be a stabilizing factor. This is further confirmed by cyclic voltammetry (CV) and AC impedance spectra analysis.     

Net Carbon Sequestration Potential and Emissions in Home Lawn Turfgrasses of the United States

Soil analyses were conducted on home lawns across diverse ecoregions of the U.S. to determine the soil organic carbon (SOC) sink capacity of turfgrass soils. Establishment of lawns sequestered SOC over time. Due to variations in ecoregions, sequestration rates varied among sites from 0.9 Mg carbon (C) ha^?1 year^?1 to 5.4 Mg C ha^?1 year^?1. Potential SOC sink capacity also varied among sites ranging from 20.8 ± 1.0–96.3 ± 6.0 Mg C ha^?1. Average sequestration rate and sink capacity for all sites sampled were 2.8 ± 0.3 Mg C ha^?1 year^?1 and 45.8 ± 3.5 Mg C ha^?1, respectively. Additionally, the hidden carbon costs (HCC) due to lawn mowing (189.7 kg Ce (carbon equivalent) ha^?1 year^?1) and fertilizer use (63.6 kg Ce ha^?1 year^?1) for all sites totaled 254.3 kg Ce ha^?1 year^?1. Considering home lawn SOC sink capacity and HCC, mean home lawn sequestration was completely negated 184 years post establishment. The potential SOC sink capacity of home lawns in the U.S. was estimated at 496.3 Tg C, with HCC of between 2,504.1 Gg Ce year^?1 under low management regimes and 7551.4 Gg Ce year^?1 under high management. This leads to a carbon-positive system for between 66 and 199 years in U.S. home lawns. More efficient and reduction of C-intensive maintenance practices could increase the overall sequestration longevity of home lawns and improve their climate change mitigation potential.     

Assessment of biomass and lipid productivity and biodiesel quality of an indigenous microalga Chlorella sorokiniana MIC-G5

Generation of biodiesel from microalgae has been extensively investigated; however, its quality is often not suitable for use as fuel. Our investigation involved the evaluation of biodiesel quality using a native isolate Chlorella sorokiniana MIC-G5, as specified by American Society for Testing and Materials (ASTM), after transesterification of lipids with methanol, in the presence of sodium methoxide. Total quantity of lipids extracted from dry biomass, of approximately 410–450 mg g^?1 was characterized using FTIR and ¹H NMR. After transesterification, the total saturated and unsaturated fatty acid methyl esters (FAMEs) were 43% and 57%, respectively. The major FAMEs present in the biodiesel were methyl palmitate (C16:0), methyl oleate (C18:1), and methyl linoleate (C18:2), and the ¹H NMR spectra matched with criteria prescribed for high-quality biodiesel. The biodiesel exhibited a density of 0.873 g cm^–3, viscosity of 3.418 mm² s^?1, cetane number (CN) of 57.85, high heating value (HHV) of 40.25, iodine value of 71.823 g I₂ 100 g^?1, degree of unsaturation (DU) of 58%, and a cold filter plugging point (CFPP) of –5.22°C. Critical fuel parameters, including oxidation stability, CN, HHV, iodine value, flash point, cloud point, pour point, density, and viscosity were in accordance with the methyl ester composition and structural configuration. Hence, C. sorokiniana can be a promising feedstock for biodiesel generation.     

The convective hot air drying of Lactuca sativa slices

The storage of fresh agricultural products is not easy because of its high moisture. Dehydration is an efficient preservation method. The investigation of drying modeling and transfer characteristics are important for selecting operating conditions and equipment design. The drying behavior of Lactuca sativa slices, with the thickness of 2 mm, was investigated at 60.0–80.0°C and 0.60–1.04 m sec^?1 velocity in a convective hot air drier. The mass transfer during the drying process was described using six thin drying models. The convective heat transfer coefficient α and mass transfer coefficient k_H were finally calculated. The results showed that the drying process could be separated into three stages including accelerating rate, constant rate, and falling rate period, which was influenced by hot air temperature and velocity, and the Modi?ed Page model agreed well with the experimental data. When the operating temperature was increased from 60.0°C to 80.0°C, α was found increased from 88.07 to 107.93 W·m^?2·K^?1, and k_H increased from 46.32 × 10^–3 to 68.04 × 10^–3 kg·m^?2·sec^?1·ΔH^?1. With the increase of air velocity from 0.60 to 1.04 m·sec^?1, α was increased from 78.85 to 101.35 W·m^?2·K^?1, and k_H was enhanced from 51.78 × 10^–3 to 65.85 × 10^–3 kg·m^?2·sec^?1·ΔH^?1.     

Pyrolysis of commingled waste textile fibers in a batch reactor: Analysis of the pyrolysis gases and solid product

The main object of this study was the investigation of the thermal recycling of commingled waste textile fibers, with the aim of the production of useful end products. Differential scanning calorimetry/Thermo gravimetric analysis (DSC/TGA) was applied to determine the thermal degradation characteristics of the commingled waste textile fibers and there are two peaks located at the temperature ranges of 299–360°C and 399–500°C. Commingled waste fiber was pyrolyzed in a nitrogen atmosphere in relation to three different temperatures (500, 600, and 700°C), heating rates (25 and 50°C min^?1), and retention times (15 and 30 min). The effect of the experimental conditions such as pyrolysis temperature, heating rates, and retention time on the formation of char and gas--liquid products was investigated and the product yields were determined from the rate of the weight loss. The highest conversion rate 82.9 wt.% liquid--gas product and 17.1 wt.% char product was achieved at 700°C. Pyrolysis gases were taken for every 7, 15, and 25 min and were analyzed for major components such as CO, CO₂, CH₄, and H₂ by gas chromatography. The pyrolysis char called as carbon black derived from the pyrolysis of commingled waste textile fibers was analyzed for a range of properties, including the elemental analysis, moisture content, ash content, calorific value, and trace metal analysis.     

Phosphorus-doped graphene supported palladium (Pd/PG) electrocatalyst for the hydrogen evolution reaction in PEM water electrolysis

PEM water electrolysis is one of the most efficient methods for the production of hydrogen because of produced high purity of the gases and environmentally friendly. In the present study, Phosphorus-doped Graphene (PG) was synthesized by thermal annealing of triphenylphosphine (TPP) and graphene oxide (GO). The PG supported palladium (Pd/PG) electrocatalysts were synthesized by chemical reduction method and used as the cathode for hydrogen evolution reaction (HER) electrode. Structural properties and electrochemical performances of the synthesized Pd/PG electrocatalyst were studied by FE-SEM, EDS, ICP, FT-IR, XRD, and Cyclic voltammetry (CV) methods, respectively. The membrane electrode assemblies (MEA’s) were fabricated using Pd/PG as cathode for HER electrode and RuO₂ as anode for OER electrode. Also, their electrochemical performances along with the corresponding hydrogen yields were evaluated in single cell PEM water electrolyzer at various experimental conditions such as different current densities from 0.1 to 2.0 A cm^?2 and temperatures (28–80°C). The synthesized Pd/PG electrocatalyst was observed a current density of 1 A cm^?2 with 1.95 V at 80°C. Further, long-term stability studies were carried out continuously up to 2000 h which showed a reasonable stability. Hence, the synthesized Pd/PG can be used as an alternative to Pt-based electrocatalysts for the HER in PEM water electrolysis.     

Catalytic degradation of toxic organic dye using an aluminum-doped Cu0.4Zn0.6-xAlxFe2O4 (x = 0.0, 0.2, 0.4, 0.6) spinel ferrite in a photo-Fenton system

Catalytic activity of spinel ferrite in breaking down toxic dye materials are promising due to their uniqueness. In this study, aluminum-doped copper zinc ferrite, Cu_0.4Zn_0.6-xAl_xFe₂O₄ (x = 0.0, 0.2, 0.4, 0.6), a catalyst for toxic dye degradation is synthesized through chemical co-precipitation route. The formation of the spinel ferrite catalyst is initially confirmed by Fourier transform infrared spectra, which shows the frequency of metal-oxygen bond vibration at 539 and 427 cm⁻¹ attributed to the tetrahedral and octahedral sites respectively. Higher intensity sharp peak of X-ray diffraction for (311) plane is the evidence for the phase purity and the formation of spinel ferrite. The crystallite size is found to decrease with the increase of Al³⁺ ion. The surface structure of the obtained particles is investigated using a scanning electron microscope. Analyses of the material's magnetic characteristics using a vibrating sample magnetometer (VSM) revealed that it is, in fact, a soft magnet, as evidenced by the loop of its hysteresis, which is narrow. The catalytic degradation of methylene blue dye under the mechanism of the photo-Fenton process is studied with the obtained spinel ferrites and the result is found to be as high as 96.5%. The process follows pseudo-second order kinetics and the Langmuir isotherm.     

Dry reforming of methane over oil palm shell activated carbon and ZSM-5 supported cobalt catalysts

In this study, cobalt supported oil palm shell activated carbon (Co/OPS-AC) and ZSM-5 zeolite (Co/ZSM-5) catalysts have been prepared for dry reforming of methane. Cobalt ratios of 6.0 and 14.0 wt% were deposited via wet impregnation method to the OPS-AC and ZSM-5 catalysts. The catalysts were characterized by XRD, N₂ adsorption--desorption isotherms, BET surface area, SEM, FESEM-EDX, TPR-H₂, and TPD-NH₃. The dry reforming of methane was performed using a micro reactor system under the condition of 10,000 ml/h.g-cat, 3 atm, CH₄/CO₂ ratio of 1.2:1.0 and temperature range from 923 K to 1023 K. The gaseous products were analyzed by gas chromatography (GC) with thermal conductivity detector (TCD) and further quantified to determine the conversions of CH₄ and CO₂, and the yields of CO and H₂. Experimental results revealed both catalysts exhibited lower conversions of CO₂ and CH₄ with the increase in temperature from 923 K to 1023 K. The reduced conversions may be due to the formation of carboneous substance on the catalyst known as coking. Comparatively, Co/OPS-AC gave higher conversions of CO₂ and CH₄ as well as higher yields of H₂ and CO as it has a higher surface area than Co/ZSM-5 which subsequently rendered higher activity for the reforming of methane. With the increasing cobalt loadings and reaction temperature, OPS-AC(14) catalyst exhibited improved activity and H₂/CO ratio. Based on these results, cobalt supported OPS activated carbon catalyst was suggested to be more effective for CO₂ and CH₄ conversions.     

Effects of alkali promoters on the textural and catalytic properties of mesoporous Fe–Al–Cu catalysts for water gas shift reaction

Mesoporous Fe₂O₃–Al₂O₃–CuO catalysts promoted with alkali oxides were synthesized and used in water gas shift reaction (WGSR) at high temperatures for hydrogen purification. These chromium-free catalysts were characterized using nitrogen adsorption/desorption, hydrogen temperature programmed reduction, X-ray diffraction (XRD), and transmission electron microscopy techniques. The synthesized catalysts with narrow single-modal pore size distribution in mesopore region possessed high specific surface area. The catalytic results revealed that except Cs, the addition of other alkali promoters declined the catalytic activity. However, all catalysts showed higher catalytic performance than the conventional commercial catalyst. The results showed an optimum content of Cs promoter (3 wt.%) for the promoted Fe–Al–Cu catalyst (3 wt.% Cs-FAC), which exhibited the highest activity in WGSR at high temperature.     

Preparation and characterization of activated carbon from a new raw lignocellulosic material: Flamboyant (Delonix regia) pods

Activated carbons were prepared from flamboyant pods by NaOH activation at three different NaOH:char ratios: 1:1 (AC-1), 2:1 (AC-2), and 3:1 (AC-3). The properties of these carbons, including BET surface area, pore volume, pore size distribution, and pore diameter, were characterized from N₂ adsorption isotherms. The activated carbons obtained were essentially microporous and had BET surface area ranging from 303 to 2463 m² g⁻¹.¹³C (CP/MAS and MAS) solid-state NMR shows that the lignocellulosic structures were completely transformed into a polycyclic material after activation process, thermogravimetry shows a high thermal resistance, Boehm titration and Fourier-transform infrared spectroscopy allowed characterizing the presence of functional groups on the surface of activated carbons. Scanning electron microscopy images showed a high pore development. The experimental results indicated the potential use of flamboyant pods as a precursor material in the preparation of activated carbon.     

Groundwater characterization in major industrial and residential locations of Lagos metropolis

This study investigated the quality of groundwater collected from two industrial and residential locations, each within the Lagos metropolis. Prescribed standard procedures of the American Public Health Association (APHA) were used to measure the physicochemical parameters of each of the groundwater samples, which include pH, electrical conductivity (EC), dissolved oxygen, total dissolved solids (TDS), biological oxygen demand, chemical oxygen demand; the anions chloride (Cl^?), nitrate (NO₃^?), sulfate (SO₄^?), and phosphate (PO₄^?); and heavy metals copper (Cu), zinc (Zn), lead (Pb), manganese (Mn), iron (Fe), cobalt (Co), cadmium (Cd), and chromium (Cr). Based on the laboratory analysis, the physicochemical parameters that were measured were within the permissible ranges specified by the World Health Organization and the Nigerian Standard for Drinking Water Quality Standards Organization of Nigeria (SON), except for pH, TDS, EC, Pb, Mn, and Fe for groundwater samples from the industrial locations and for pH, Pb, Mn, and Fe for residential locations. The elevated concentrations of TDS and EC reported for groundwater samples from industrial locations were attributed to the heavy discharge of effluents from nearby industrial treatment plants as well as the dissolution of ionic heavy metals from industrial activities involving the use of heavy machines. Statistical analysis using Pearson's correlation revealed the physicochemical parameters to be moderately and strongly correlated with one another at either p < .05 or < .01. In conclusion, groundwater samples from residential locations are more suitable for drinking than those from industrial locations.     

Effect of Prescribed Fire on Soil Properties and N Transformation in Two Vegetation Types in South China

Prescribed fire is a common site preparation practice in forest management in southern China. However, the effect of fire on soil properties and N transformations is still poorly understood in this region. In this study, soil properties and N transformations in burned and unburned site of two vegetation types (Eucalyptus plantation and shrubland) were compared in rainy and dry seasons after 2 years’ prescribed fire. Soil pH and soil NH₄-N were all higher in the burned site compared to the unburned control. Furthermore, burned sites had 30–40 % lower of soil total phosphorus than conspecific unburned sites. There was no difference in soil organic matter, total N, soil exchangeable cations, available P or NO₃-N. Nitrogen mineralization rate of 0–5 cm soil in the unburned site ranged from 8.24 to 11.6 mg N kg^?1 soil month^?1 in the rainy season, compared to a lower level of 4.82–5.25 mg N kg^?1 soil month^?1 in the burned sites. In contrast, 0–5 cm layer nitrification rate was overall 2.47 mg N kg^?1 soil month^?1 in the rainy season, and was not significantly affected by burning. The reduced understory vegetation coverage after burning may be responsible for the higher soil NH₄-N in the burned site. This study highlights that a better understanding the effect of prescribed burning on soil nutrients cycling would provide a critical foundation for management decision and be beneficial to afforestation in southern China.     

Effect of Fenton pretreatment on anaerobic digestion of olive mill wastewater and olive mill solid waste in mesophilic conditions

The olive mill waste (OMW) generated from olive oil extraction process constitutes a major environmental concern owing to its high organic and mineral matters and acidic pH. Anaerobic digestion (AD) is a main treatment for reducing the organic matter and toxic substances contained in OMW and generating at the same time, energy in the form of biogas. AD of OMW that contains lignocellulose is limited by the rate of hydrolysis due to their recalcitrant structure. This study is devoted to the effect of Fenton process (FP) pretreatment on olive mill wastewater (OMSW) /olive mill solid waste (OMWW) co-digestion to improve their digestibility and in this way the biogas production. The FP pretreatment was performed in batch mode at 25°C, various H₂O₂/[Fe²⁺] ratios (100–1200), catalyst concentration ([Fe²⁺]) ranging from 0.25 to 2 mM, reaction time varying from 30 to150 min, and different pH (3–11). The best performance was obtained with H₂O₂/[Fe²⁺] = 1000, [Fe²⁺] = 1.5 mM, 120 min, and pH 3. Biochemical methane potential (BMP) tests conducted in batch wise digester and at mesophilic conditions (37 °C) showed that cumulative biogas and methane production were higher without FP treatment, and correspond to 699 and 416 mL/g VS, respectively. However, pre-treated OMSW results into an increase of 24% of methane yield. After 30 days of AD, the methane yield was 63%, 54%, and 48%, respectively, for OMSW treated without iron precipitation, with iron precipitation and untreated OMSW sample.     

ALGAL BIOASSAY AND GROSS PRODUCTIVITY EXPERIMENTS USING SEWAGE EFFLUENT IN A MICHIGAN WETLAND'

ABSTRACT: One component of the filamentous algal community of a northern fen ecosystem in central Michigan was studied under conditions of nutrient enrichment by secondarily treated sewage effluent during one growing season. The productivity of Cladophora spp. measured by continuous flow bioassay was 2.6 g dry weight m day at the site of effluent addition compared to 0.085 g m day at the control site. Under conditions of nutrient enrichment, uptake by bioassay Cladophora spp. averaged 12 mg m^?2day^?1for phosphorus and 55 mg m^?2day^?1for nitrogen, compared to 0.01 mg m^?2 day^?1and 0.16 mg m^?2day^?1for phosphorus and nitrogen, respectively, in the control area. At the end of the growing season approximately 4.3 g N m^?2 and 0.96 g P m^?2were immobilized in Cladophora algal biomass. Algal growth temporarily immobilized 3.0 percent of the nitrogen and 1.0 percent of the phosphorus added as sewage effluent. Gross productivity of surface water in the fen averaged 1.5 g O₂m^?2day^?1at the nutrient enriched site, compared to 0.5 g O₂ m^?2day^?1at the control area. Gross productivity, community respiration and reaeration constant values in the fen were similar to data collected by other researchers in shallow water aquatic systems, but only at the fertilized sites.     

BIOGEOCIIEMISTRY OF AN OLD-GROWTH FORESTED WATERSHED,OLYMPIC NATIONAL PARK,WASHINGTON1

ABSTRACT: The biogeochemistry of a coastal old-growth forested watershed in Olympic National Park, Washington, was examined. Objectives were to determine: (1) concentrations of major cations and anions and dissolved organic C (DOC) in precipitation, throughfall, stemflow, soil solution and the stream; (2) nutrient input/output budgets; and (3) nutrient retention mechanisms in the watershed. Stemilow was more acidic (pH 4.0–4.5) than throughfall (pH 5.1) and precipitation (pH 5.3). Organic acids were important contributors to acidity in throughfall and stemflow and tree species influenced pH. Soil solution pH averaged 6.2 at 40 cm depth. Stream pH was higher (7.6). Sodium (54.0 μeq L-¹) and Cl (57.6 μeq L^?1) were the dominant ions in precipitation, reflecting the close proximity to the ocean. Throughfall and stemflow were generally enriched in cations, especially K. Cation concentrations in soil solutions were generally less than those in stemilow. Ion concentrations increased in the stream. Dominant ions were Ca (759.7 μeq L^?1), Na (174.4 μeq L^?1), HCO₃ (592.0 μeq L^?1), and SO₄ (331.5 μeq L^?1) with seasonal peaks in the fall. Bedrock weathering strongly influenced stream chemistry. Highest average NO₃ concentrations were in the stream (5.2 μeq L^?1) with seasonal peaks in the fall and lowest concentrations in the growing season. Nitrogen losses were similar to inputs; annual inputs were 4.8 kg/ha (not including fixation) and stream losses were 7.1 kg/ha. Despite the age and successional status of the forest, plant uptake is an important N retention mechanism in this watershed.     

Transesterification of Pistacia chinensis seed oil using a porous cellulose-based magnetic heterogeneous catalyst

In the present work, a novel cellulose-based porous heterogeneous solid acid catalyst encapsulation of ferriferous oxide (Fe₃O₄) and sulfonated graphene (GO-SO₃H) into cellulose to form composite porous microspheres catalyst (GO-SO₃H/CM@Fe₃O₄)was synthesized and evaluated for biodiesel production from Pistacia chinensis seed oil. The SEM, EDS and FTIR analysis revealed that the catalyst GO-SO₃H/CM@Fe₃O₄ owned stronger active sites and GO-SO₃H dispersed well in porous surface and inside of cellulose support. Under the optimum conditions, microwave-assisted transesterification process was carried out with the best catalyst amount, i.e. 5 wt% GO-SO₃H/CM@Fe₃O₄ (weight ratio of GO-SO₃H/cellulose), and conversion yield reached 94%. The prepared catalyst could be easily separated from reaction solution by extra magnetic field and reclaimed at least five runs.     

Estimating Annual Groundwater Evapotranspiration from Phreatophytes in the Great Basin Using Landsat and Flux Tower Measurements

Escalating concerns about water supplies in the Great Basin have prompted numerous water budget studies focused on groundwater recharge and discharge. For many hydrographic areas (HAs) in the Great Basin, most of the recharge is discharged by bare soil evaporation and evapotranspiration (ET) from phreatophyte vegetation. Estimating recharge from precipitation in a given HA is difficult and often has significant uncertainty, therefore it is often quantified by estimating the natural discharge. As such, remote sensing applications for spatially distributing flux tower estimates of ET and groundwater ET (ET_g) across phreatophyte areas are becoming more common. We build on previous studies and develop a transferable empirical relationship with uncertainty bounds between flux tower estimates of ET and a remotely sensed vegetation index, Enhanced Vegetation Index (EVI). Energy balance‐corrected ET measured from 40 flux tower site‐year combinations in the Great Basin was statistically correlated with EVI derived from Landsat imagery (r² = 0.97). Application of the relationship to estimate mean‐annual ET_g from four HAs in western and eastern Nevada is highlighted and results are compared with previous estimates. Uncertainty bounds about the estimated mean ET_g allow investigators to evaluate if independent groundwater discharge estimates are “believable” and will ultimately assist local, state, and federal agencies to evaluate expert witness reports of ET_g, along with providing new first‐order estimates of ET_g.     

Investigating the quantitative and qualitative status of effluent in the wastewater treatment plant in Iran Central Iron Ore

The aim of present study was to investigate the quality of the produced effluent from different units of the Iran Central Iron Ore in Bafq city and comparison of effluent with the standards. This study presents the physicochemical and biological parameters data of effluent of three Sequencing batch reactors (SBR) with a capacity of 160 m³?d^?1. Most common parameters include pH, total suspended solids (TSS), total nitrogen (TN), total phosphorus (TP), biochemical oxygen demand (BOD₅), chemical oxygen demand (COD), heavy metals, and total coliforms and fecal coliforms as biological indicators. Then, for each SBR system, the average of each parameter was determined, and results were compared with the standard recommended by the Iranian Environmental Protection Agency. Based on the results, some of the parameters, including BOD₅, COD, and TSS in the wastewater treatment plant (WWTP) effluent, are higher than the permitted amount for discharge to the surface water. Considering the BOD₅, COD, and TSS concentration in WWTPs, the treated wastewater is only suitable for agricultural and irrigation use. Therefore, wastewater produced by Iran Central Iron Ore Co. will need additional treatment to achieve standard quality of water before discharge in surface water and adsorbent well.     

Hydrologic Controls on Nitrogen and Phosphorous Dynamics in Relict Oxbow Wetlands Adjacent to an Urban Restored Stream

Although wetlands are known to be sinks for nitrogen (N) and phosphorus (P), their function in urban watersheds remains unclear. We analyzed water and nitrate (NO₃^?) and phosphate (PO₄^3?) dynamics during precipitation events in two oxbow wetlands that were created during geomorphic stream restoration in Baltimore County, Maryland that varied in the nature and extent of connectivity to the adjacent stream. Oxbow 1 (Ox1) received 1.6‐4.2% and Oxbow 2 (Ox2) received 4.2‐7.4% of cumulative streamflow during storm events from subsurface seepage (Ox1) and surface flow (Ox2). The retention time of incoming stormwater ranged from 0.2 to 6.7 days in Ox1 and 1.8 to 4.3 days in Ox2. Retention rates in the wetlands ranged from 0.25 to 2.74 g N/m²/day in Ox1 and 0.29 to 1.94 g N/m²/day in Ox2. Percent retention of the NO₃^?‐N load that entered the wetlands during the storm events ranged from 64 to 87% and 23 to 26%, in Ox1 and Ox2, respectively. During all four storm events, Ox1 and Ox2 were a small net source of dissolved PO₄^3? to the adjacent stream (i.e., more P exited than entered the wetland), releasing P at a rate of 0.23‐20.83 mg P/m²/day and 3.43‐24.84 mg P/m²/day, respectively. N and P removal efficiency of the oxbows were regulated by hydrologic connectivity, hydraulic loading, and retention time. Incidental oxbow wetlands have potential to receive urban stream and storm flow and to be significant N sinks, but they may be sources of P in urban watersheds.     

Synthesis and characterization of multi-walled carbon nanotubes from silkworm cocoons to use as the cathode material for Al-air battery

ABSTRACT

Carbon nanotubes have been synthesized by chemical vapor deposition at 850°C using silkworm cocoons as a precursor. The impregnation method with 3 wt% ferrocene as a catalyst was utilized for growth of carbon nanotubes. The flow rates of C₂H₂, H₂, and N₂ were fixed at 100, 150, and 350 ml/min, respectively. Morphology, microstructure and quality of the synthesized carbon nanotubes were investigated by scanning electron microscopy, transmission electron microscopy, and Raman spectroscopy techniques. Results showed that the prepared carbon nanotubes were multiwalled and good graphitic quality. When used as the cathode material for aluminum-air battery, prepared carbon nanotubes cathode exhibited higher current density than commercial graphite cathode. Based on our study, there is a successful conversion of silkworm cocoons into value-added nanomaterial products, promoting the natural biotechnological materials.