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Effects of Reed Sedge Peat on Lambs at Weaning with Regard to Stress and Apparent Nutrient DigestibilityPrice, Rhianwedd O 03 May 2019 (has links)
For this study 14 lambs were obtained, which were split into two groups; a control group (CON) and a group that was supplemented Reed Sedge Peat (RSP). We wanted to test whether RSP could decrease stress at weaning, increase immune response and also increase digestibility of the animal. Lambs were subjected to an ACTH challenge 48 hours post weaning. After weaning (d 28 of study) 10 of the lambs (5 CON; 5 RSP) also underwent a digestibility challenge. We found that there was no difference (P = 0.8764) within cortisol concentration during the weaning portion of the study between the two treatment groups. During the ACTH challenger there was a difference between RSP group and CON, where RSP had a decrease in cortisol concentration (P = 0.0892). There was no difference in blood cell parameters, except for SEG, % (P = 0.0890) where RSP had greater % of SEG than CON group. Within the digestibility trail there was a decrease in digestibility within the RSP group compared to CON, within DM, OM, NDF and ADF (P = 0.0458; P = 0.0430; P = 0.0509; P = 0.0786; respectively).
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Sonochemical remediation of Mercury from contaminated sedimentsHe, Ziqi 20 September 2006 (has links)
No description available.
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Sorption of Metal Ions onto Sedimentary Rock in the Presence of Gamma-Irradiated Humic Acid / ガンマ線照射したフミン酸存在下における金属イオンの堆積岩への収着に関する研究Zhao, Qi 23 May 2022 (has links)
京都大学 / 新制・課程博士 / 博士(工学) / 甲第24104号 / 工博第5026号 / 新制||工||1784(附属図書館) / 京都大学大学院工学研究科原子核工学専攻 / (主査)教授 佐々木 隆之, 教授 横峯 健彦, 准教授 小林 大志 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DFAM
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Metal Extraction From Soil Samples By Chelation in a Microwave SystemChatreewongsin, Urai 01 May 2000 (has links)
This work involves the combination of chelation and microwave extraction as a technique for extracting adsorbed metals in soil. It has been termed in this work, Chelate Assisted Microwave Extraction (CAME). Unlike other extraction methods, CAME is able to differentiate between anthropological and geological trace metals.
The method has been applied to major sample matrices included three types of soils (Bertie Sandy Loam, Davidson Silty Clay, and Davidson Clayey Loam) as well as sea sand, alumina, and iron oxide. In order to investigate the effects of sorptive coatings on metal concentrations, a sample set was first treated with humic acids, which represented organic coated materials. Afterwards, copper (II) solutions were spiked to both untreated and treated matrices and the efficiencies of recoveries were studied. Metal determinations were performed by Inductively Coupled Plasma-Atomic Emission Spectrophotometry (ICP-AES).
Initial studies of control (untreated soil) and long-term Cu amended (spiked) Bertie Sandy Loam (BSL) indicated that extraction efficiencies were method dependent. Ethylenediaminetetraacetic acid (EDTA) was a primary chelating agent used for method comparisons. Extracting solutions having a pH range from 7.8 to 10.1 did not affect the EDTA-microwave method, but the increase in pH enhanced Cu removal by the EDTA-shaking extraction method which was a conventional chelation using a mechanical shaker. With the EDTA-microwave method, complete extraction was achieved in a short period of time (20 minutes). Compared to the EDTA-shaking method using two sandy soils, the EDTA-microwave method proved to be more efficient in extracting sorbed metals in soils (5.9 vs. 4.6 µg/g for the control BSL and 37.5 vs. 27.8 µg/g for the amended BSL.
FT-IR and C13 NMR were used to characterize extracted and commercially available humic acids. The latter was employed to prepare the humate coated materials. Iron oxide containing materials such as Davidson Silty Clay (DSC), Davidson Clayey Loam (DCL), and iron oxide (Fe2O3), showed extremely high adsorption capabilities for humic acids, while sea sand, Bertie Sandy Loam, and alumina (Al₂O₃) provided lower adsorption capabilities for humic acids. Two sets of uncoated and humate coated materials were used for Cu spiking procedures using 0.001 M Cu (II) at pH 5.3 for 24 hour-equilibration. Three original soils and alumina showed high adsorption capabilities for Cu (II). The presence of coated humate helped increase Cu adsorption capabilities of these soils, but diminished the ability of alumina to react with Cu (II) ions. For HA-uncoated matrices, iron oxide had a higher Cu adsorption capability than sea sand but less than real soils. Humate coating improved Cu adsorption capabilities of not only real soils but iron oxide and sea sand as well.
Lastly, the developed method named Chelate Assisted Microwave Extraction (CAME) was further examined and optimized. Several samples were investigated for extraction efficiencies. A two-step extraction, applying 120 W for 5 min followed by 60 W for 10 min, was efficient in removing sorbed metals from different matrices regardless of sorptive oxide and organic components. Concentrations of chelating agents slightly affected percent metal removal; however, there was no significant difference in results obtained using EDTA or diethylenetriaminepentaacetic acid (DTPA). Recoveries of spiked metals (Cu and Cd) ranged from 96 to 107%. Using the untreated (control) Davidson Silty Clay and Bertie Sandy Loam, the comparison of other chelating solutions were made. Clearly, CAME was promising and proved to be a good alternative to classical shaking method for extracting adsorbed metals from soils. / Ph. D.
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An integrated plant nutrition system (IPNS) for corn and cannabis in the Mid-Atlantic USADa Cunha Leme Filho, Jose Franco 29 May 2020 (has links)
Agroecosystem and cycling loops are open when considering the reutilization of inputs in farming areas. Non-renewable resources have been transformed or relocated from the air, water and land into the system and are flowing out as wastes rather than reusable, recyclable resources. Therefore, current trends in agriculture have moved towards more sustainable cultivation systems with higher efficiency of input use, since mineral nutrient losses due to runoff, leaching, erosion and gas emissions are leading to environmental degradation. A huge variety of materials can serve as a crop nutrient supply and they can be derived from different resources. The integrated plant nutrition system (IPNS) thrives tailoring plant nutrition and soil fertility management, taking advantage of the conjunctive and harmonious use of inorganic, organic and biological resources. We hypothesize that the synergetic effects of the combination of humic acid HA + biofertilizer will improve plant agronomic outcomes when comparing the application of each product alone. We initiated this project conducting a greenhouse study and field experiments evaluating the effects of an IPNS on corn. Posteriorly, the positive results in terms of corn biomass increasing, led to another greenhouse study addressing cannabis (Cannabis sativa L.) due its valuable biomass as an end/selling product.
The greenhouse studies evaluated the effects of commercial synthetic fertilizer, HA, compost/manure teas and bioinoculant as inorganic, organic and biological resources, respectively, and their synergy on corn and cannabis early development under a period of water deficit stress. Generally, for both studies, when compared to the control values, the use of HA, biofertilizers and the integration of both substances generated significantly greater early season plant height, chlorophyll content and photosynthetic efficiency.
The three-year field trial investigated the effects of nitrogen (N) fertilizer, HA, compost/manure teas and bioinoculant as inorganic, organic and biological resources, respectively and their synergy on corn growth. The individual and integrated application of HA and biofertilizer generally influenced corn development, to varying degrees. In 2017, corn height, NDVI, greenness and vigor were sensitive to the application of these biostimulants in different magnitudes and growth stages, however grain yield and nutrient content were not affected. In combined studies from 2018 and 2019 corn height was not impacted by biostimulant application but NDVI, photosynthetic efficiency, greenness and vigor were affected at different doses and corn growth stages. Only one treatment integrating HA + biofertilizer led to increased grain yield.
In sum, these studies provided evidence that the individual and combined application of HA and biofertilizer can positively influence corn and cannabis growth most likely due to their plant biostimulant effects. However, the current study cannot conclusively affirm that the integrated use of HA and biofertilizers following the IPNS is a superior practice than the application of each compound individually and further studies should be conducted to validate these findings. / Doctor of Philosophy / The status of the corn (Zea mays L.) demand in Virginia and the Mid-Atlantic region is currently in deficit regarding the production in this area. This demand is exceeding supply by approximately 150%, then increasing feed grain yield and consequently production in the region can be simultaneously beneficial to crop farmers, end-users and the entire food supply chain. Furthermore, the consumer market is becoming more aware about sustainable practices for food production, which encourages producers to adopt agricultural practices that can minimize negative environmental impacts. This scenario enforces the scientific community's responsibility to test and develop environmental-friendly methods able to increase fertilization efficiency, decreasing the use in synthetic inputs but maintaining yield. The integrated plant nutrition system (IPNS) implements the combined and harmonious use of inorganic, organic and biological resources to take advantage of the potential synergetic effects. We conducted greenhouse studies and field experiments evaluating the effects of an IPNS on corn, and posteriorly based on the preliminary results obtained with corn, a greenhouse study addressing cannabis (Cannabis sativa L.) was also carried out.
The greenhouse studies evaluated the effects of commercial synthetic fertilizer, humic acid (HA), compost/manure teas and bioinoculant as inorganic, organic and biological resources, respectively, and their synergy on corn and cannabis growth under a period of drought. Generally, for both studies, when comparing to the control values, the use of HA, biofertilizers and the integration of both compounds generated significantly greater early season plant height and photosynthesis measurements.
The three-year field trial investigated the effects of nitrogen (N) fertilizer, HA, compost/manure teas and bioinoculant as inorganic, organic and biological resources, respectively and their synergy on corn growth. The individual and combined application of HA and biofertilizer generally influenced corn development, to varying degrees. In 2017, corn height, vegetation index, greenness and vigor were sensitive to the application of these biostimulants in different magnitudes and growth stages, however grain yield and nutrient content were not affected. In combined studies from 2018 and 2019 corn height was not impacted by biostimulant application but vegetation index, photosynthetic efficiency, greenness and vigor were affected at different doses and corn growth stages. Only one treatment combining HA + biofertilizer led to increased grain yield.
In sum, these studies provided evidence that the individual and combined application of HA and biofertilizer can positively influence corn and cannabis growth most likely due their plant biostimulant effects. Even though, the current study cannot affirm that the combined use of HA and biofertilizers following the IPNS is a better practice than the application of each compound individually, this practice can be a more sustainable alternative to fit in the conventional farming scene.
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Aqueous Silica in the Environment: Effects on Iron Hydroxide Surface Chemistry and Implications for Natural and Engineered SystemsDavis, Christina Clarkson 14 July 2000 (has links)
Aqueous silica is present in all natural waters and exhibits a high affinity for the surfaces of iron oxides. Therefore, it is expected to play an important role in environmental systems. Experiments were conducted to investigate the fundamentals of silica sorption onto pre-formed ferric hydroxide at pH 5.0-9.5 and silica concentrations of 0-200 mg/L as SiO₂. Over the entire pH range studied, sorption densities exceeding monolayer sorption were observed at silica levels typical of natural waters. Under some circumstances, sorption exceeded a monolayer while the particle zeta potential remained positive, a phenomenon which is inconsistent with available models. To address this deficiency, an extended surface complexation model was formulated in which soluble dimeric silica sorbs directly to iron surface sites. This model fits sorption density data up to 0.40 mol SiO₂/mol Fe, and it accurately predicts trends in zeta potential and the observed H⁺ release during silica sorption to ferric hydroxide at pH 5.0 and 6.0.
A second phase of research was aimed at identifying the practical implications of silica sorption to iron hydroxide in natural and engineered systems. Two types of surfaces were prepared by exposing pre-formed Fe(OH)₃ to aqueous silica (0-200 mg/L as SiO₂) for periods of 1.5 hours or 50 days. The concentration of pre-formed iron passing through a 0.45 micron pore size filter at pH 6.0-9.5 increased as the solids aged in the presence of silica. Consistent with formation of small, stable colloids, "soluble" iron concentrations exceeded 0.2 mg/L only at zeta potentials <span style="text-decoration:underline"><</span> -15 mV. When arsenate was added to iron hydroxide particles equilibrated with silica for 1.5 hours, percentage arsenate removals were high. In contrast, arsenate removals decreased markedly as pH and silica concentrations increased if silica was pre-equilibrated with the iron for 50 days. Trends in percentage removal of humic substances were similar. Competition for sorption sites was the main cause of hindered anionic contaminant removal. However, interference with hydrolysis and precipitation are expected to be important under some circumstances, particularly during water treatment. / Master of Science
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Creeping Bentgrass, Kentucky Bluegrass and Tall Fescue Responses to Plant Growth Stimulants Under Deficit IrrigationLaBranche, Adrienne Janel 02 May 2005 (has links)
A four-year drought, increasing population and shifting climate has spurred water conservation practices within Virginia. Creeping bentgrass (<i>Agrostis palustris</i> "L93"), Kentucky bluegrass (<i>Poa pratensis </i>"Midnight"), and tall fescue (<i>Festuca arundinacea</i>) Dominion blend were evaluated under deficit irrigation and upon exogenous application of plant growth stimulants (PGS), seaweed extract (SWE) + humic acid (HA), glycinebetaine (GB) and a commercial SWE product (PP). The objectives were to determine crop coefficients (K<sub>c</sub>) for creeping bentgrass fairways and tall fescue home lawns, to determine if PGS application allowed for more water conservation, and to determine if they impacted physiological function and/or root morphology.
A preliminary greenhouse experiment was conducted with creeping bentgrass and Kentucky bluegrass irrigated with 100%, 85% and 70% of evapotranspiration (ET). The study determined that an additional deficit irrigation level should be included for the field study and that GB application and 100% and 85% ET irrigation level produced the greatest creeping bentgrass root mass.
The two–year field study evaluated creeping bentgrass and tall fescue. Tall fescue home lawns could be irrigated every five days with a K<sub>c</sub> of 0.55 or once a week with a K<sub>c</sub> of 0.70. Creeping bentgrass fairways could be irrigated every four days with a K<sub>c</sub> of 0.85. Glycinebetaine application increased bentgrass rooting after planting and showed osmoprotectant properties.
Another greenhouse study evaluated five GB rates on bentgrass and tall fescue. No differences were found between the five rates and concluded that the rate utilized in the field study may be appropriate for turfgrass application. / Master of Science
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Sorption of pentachlorophenol to humic acids and subsequent effects on biodegradation and solvent extractionCrane, Cynthia E. 17 March 2010 (has links)
The focus of this research was to acquire a better understanding of the sorption and desorption of pentachlorophenol to soil organic matter. In order to separate the reactions controlling the interactions with the soil organic matter from those associated with mineral surfaces, these experiments used only humic acids extracted from soil samples. The major focus of this study was to examine the effects of solution pH, humic acid concentration and contact time on the degree of sorption. The association reactions proceeded slowly. Even after 28 days, many solutions had not attained equilibrium. An increase in the solution pH led to a reduction in the amount of partitioning onto the humic material. At solution concentrations between 100 mg/L and 800 mg/L of total organic carbon (TOC), an increase in the humic acid concentration resulted in a lower partition coefficient. However, above a concentration of 800 mg/L TOC, further increases in the amount of humic material caused enhanced sorption. The particulate humic acids demonstrated a higher affinity for the pentachlorophenol than did the dissolved polymers. In the concentrated solutions, the majority of the humic acids were present in the particulate form.
Two experiments focused on the effect of sorption on the bioavailability and solvent extraction of pentachlorophenol. The bioavailability data Suggested that the sorbed contaminant was not readily accessible to the microorganisms. The humic acids prevented the extraction of the sorbate by methyl-tert-butyl ether and methylene chloride. Recovery of the pentachlorophenol sorbed to the dissolved humic acids ranged from zero to 42.9 percent, depending on the solution pH. The removal of pentachlorophenol from the particulate matter varied from 25 percent to 90 percent. Longer contact times diminished the transfer of PCP associated with the solid humic acids to the solvent phase.
The experimental results were not consistent with a simple, one mechanism model. The best explanation of the data was provided by a model which included liquid-liquid partitioning, surface sorption, absorption, and chemisorption. The dominant process depended on the contact time, solution pH, and concentration and nature of the humic acids. / Master of Science
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Simultaneous removal process for humic acids and metal ions by adsorptionTerdkiatburana, Thanet January 2007 (has links)
Humic substances are macromolecules that naturally occur in all environments in which vegetation matter are present. In general, humic acid is part of humic substances which form the major fraction of the dissolved organic matters in surface water and represents 90% of dissolved organic carbon. Humic acid plays a fundamental role in many ecosystems since it interacts with toxic metal ions present in the system, resulting in a decrease in the bio-availability of such ions. Moreover, the availability of humic acid in water can react with other chemical compounds, such as chlorine to form trihalomethanes (including chloroform) and causes an increasing risk of cancer and may be linked to heart, lung, kidney, liver, and central nervous system damage. Therefore, humic acid removal in water treatment processes is very important in order to achieve the drinking water standards. Heavy metals are significant contaminants in aqueous system. All heavy metals can produce toxicity when ingested in sufficient quantities, but there are several important ones such as lead, mercury, copper, cadmium, arsenic, nickel and silver. These heavy metals are so pervasive and produce toxicity at low concentrations. Moreover, they may build up in biological systems and become a significant health hazard. / Adsorption is approved as an effective and simple method for water and wastewater treatment process. Many adsorbents then are developed for use in adsorption process such as montmorillonite, peat, activated carbon, etc. In this research, humic acid and heavy metals were mainly selected for adsorption study. In the sorption experiment, several adsorbents such as synthesised zeolite (SZ), natural zeolite (NZ), powdered activated carbon (PAC) and fly ash (FA), were selected to examine the application of HA and heavy metals both in individual and simultaneous adsorption, The characteristics and interactions of the adsorbents with HA and heavy metals were systematically studied by batch laboratory experiments. In the beginning, the adsorption of HA onto SZ, NZ, PAC and FA was investigated and their adsorption capacity was compared. The equilibrium adsorption of HA on SZ, NZ, PAC and FA was found to be 84.1, 67.8, 81.2 and 34.1 mg/g, respectively, at 30 oC and pH 5.0. Dynamic adsorption data show that these adsorbents could reach their adsorption equilibrium after 50 hours. From pH analysis, HA adsorption is favoured at low pH and an increase in pH will lead to the reduction of HA adsorption. SZ and NZ adsorption capacity were affected by the changing of solution temperature; however, in PAC and FA sorption study, there was no significant effect observed. Two heavy metal ions (Cu, Pb) removal by the adsorbents was then conducted. The results showed that the equilibrium sorption capacity of Cu and Pb ions on SZ, NZ, PAC and FA were 43.5, 24.2, 19.7, 28.6 and 190.7, 129.0, 76.8 mg/g, respectively at 30 oC and a pH value of 5. The appropriate pH for Cu and Pb removal was found to be 5 and 6. In most dynamic cases, these adsorbents needed at least 50 hours to reach the adsorption equilibrium. Only adsorption on FA required more than 150 hours to reach the equilibrium. / In simultaneous adsorption experiments, the influences of HA and heavy metal concentration (in the range of 10 to 50 mg/L for HA and 10 to 30 mg/l for heavy metals) on the HA-heavy metal complexation were investigated. The results demonstrated that increasing HA concentration mostly affected Cu adsorbed on SZ, FA and PAC and Pb adsorbed on SZ, NZ and PAC. For HA adsorption, the adsorption rate decreased rapidly with increased initial metal ion concentration. Moreover, the adsorption of heavy metals increased with increased heavy metals concentration in the presence of HA. In the presence of heavy metal ions, the order of HA adsorption followed PAC > FA > SZ > NZ. According to the results, the individual and simultaneous adsorption of HA and heavy metals on each adsorbent achieved a different trend. It mainly depended on the adsorption property of both adsorbates (HA and heavy metals) and adsorbents (SZ, NZ, PAC and FA) and also the operation factors such as pH, concentration, temperature and operation time. Even though this experiment could not obtain high adsorption performance, especially in coadsorption, as compared with other adsorbents, the adsorbents in this study represented a higher adsorption capacity and provide the potential for further development.
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Characterization and Removal of NOM from Raw Waters in Coastal EnvironmentsCheck, Jason Kenneth 05 April 2005 (has links)
An investigation was conducted focusing on how NOM affects coagulation in a United States south eastern coastal surface water. Current water treatment practice at Savannah Water I and D was
investigated to determine the efficacy of NOM removal using existing coagulation
methods. A robust assessment of alum and ferric sulfate for use as coagulants in the
removal of disinfection byproduct (DBP) precursor material was conducted using
composite water created from sample sites within the SWID watershed. Both coagulants
were optimized for the removal of NOM.
Pragmatic methods of NOM size analysis and its reactivity with chlorine was
investigated. UF membranes were used in conjunction with a permeation coefficient
model (PCM) to determine an apparent molecular weight distribution of NOM present in
the watershed. Individual size classes were assessed for their potential to form
trihalomethanes (THMs) upon chlorination. Coagulation using alum and ferric sulfate
was assessed to determine removal efficiency of individual NOM size classes under
various coagulation scenarios.
Finally, UV254 absorbance (UVA) was assessed to determine its potential use as an
indicator of DOC concentration in raw and treated water at SWID. Additionally, an
investigation into the relationship between specific UVA (SUVA) and THM formation
potential (THM-FP) was conducted.
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