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1

Pessarakli, Mohammad, David D. Breshears, James Walworth, Jason P. Field, and Darin J. Law. "Candidate halophytic grasses for addressing land degradation: Shoot responses of Sporobolus airoides and Paspalum vaginatum to weekly increasing NaCl concentration." TAYLOR & FRANCIS INC, 2017. http://hdl.handle.net/10150/623948.

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In many arid and semiarid regions worldwide, high levels of soil salinity is a key driver of land degradation, as well as a key impediment to re-establishing plant cover. Combating land degradation and erosion associated with soil salinity requires experimental determination of plant species that can grow in soils with high levels of salinity and can be used to re-establish plant cover. Herein, we evaluated the responses of untested candidate cultivars of two halophytic grass species to high soil salinity: alkali sacaton (Sporobolus airoides Torr.) and seashore paspalum (Paspalum vaginatum Swartz). We evaluated the growth responses of both species in a greenhouse under control (no-salt) and various levels of NaCl salinity (EC 8, 16, 24, 32, 40, and 48dSm(-1)) using Hoagland solution in a hydroponics system in a randomized complete block design trial. At all salinity levels, sacaton grass had a greater shoot height, shorter root length, lower shoot fresh and dry weights, and poorer color and general quality compared to seashore paspalum. The shoot fresh and dry weights of both grasses were greatest at the low to medium levels of salinity, with the greatest response observed at EC 16dSm(-1). At the highest level, salinity significantly reduced shoot fresh and dry weights of both grasses. Because growth of both halophytic species exhibited high tolerance to salinity stress and were stimulated under low to medium levels of salinity, both species could be considered suitable candidates for re-establishing plant cover in drylands to combat desertification and land degradation associated with high levels of soil salinity.
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2

Gunnarsson, Matilda. "Sustainability assessment of urine concentration technologies." Thesis, Uppsala universitet, Institutionen för geovetenskaper, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-447906.

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The majority of the nutrients in household wastewater are found in the urine and in order to facilitate the use the nutrients in the urine as fertilizer, the urine can be can be concentrated. To extract the nutrients from the urine, various technologies for urine concentration are being developed today. As the technologies are relatively new, urine concentration systems have not been installed on a larger scale. In this study, sustainability of three different urine concentration technologies was evaluated through a fictional case study for 2100 people that took inspiration from a planned residential area in Malmö, Sweden, where technology for urine concentration will be implemented in at least one of the buildings. The technologies were evaluated through a multi-criteria assessment (MCA), where different criteria within sustainability categories environment, technical, economic and health were determined based on the Sustainable Development Goals (SDGs). The technologies examined were alkaline dehydration, nitrification-distillation and ion-exchange using a pre-step of struvite precipitation. For the alkaline dehydration technology, fresh urine is added to an alkaline medium, in order to prevent nitrogen losses, and then dried. In the nitrification-distillation technology, stored urine is treated by first being stabilized by a partial nitrification and then distilled in order to reduce the volume. For the ion-exchange and struvite precipitation system, phosphorus is first precipitated from stored urine and nitrogen is then extracted through ion-exchange. The urine concentration technologies were assumed to be installed in semi-centralized treatment plants in basements in the residential area. The other household wastewater was assumed to be treated in the local wastewater treatment plant (WWTP). The results showed that all three urine concentration technologies may contribute to a significant increase in nitrogen recovery from the household sewer. However, this may come at the expense of increased annual costs for the population. Before it is possible to determine whether urine concentration can be an alternative as a complement to the existing wastewater treatment, further studies of the urine concentration technologies and their sustainability are required. However, this study indicated that urine concentration technologies perform well in many of the sustainability criteria examined and therefore have potential to contribute to the SDGs, especially regarding nitrogen recovery. This study can therefore be an incentive for further studies, where the sustainability of an implementation of urine concentration in Sweden is addressed.<br>Majoriteten av näringen i hushållsavloppsvattnet finns i urinen och för att underlätta användningen av växtnäringsämnena i urinen som gödningsmedel kan den koncentreras. För att utvinna näringen ur urinen utvecklas idag olika tekniker för urinkoncentrering. Då teknikerna är relativt nya har system för urinkoncentrering inte installerats i en större skala. Därför utvärderades hållbarheten för tre olika urinkoncentreringsmetoder genom en fiktiv fallstudie som innefattade 2100 personer. Fallstudien fick inspiration från ett planerat bostadsområde i Malmö, Sverige, där teknik för urinkoncentrering ska implementeras i minst en av byggnaderna. Teknikerna utvärderades genom en multikriterieanalys (MKA), där kriterier inom hållbarhetskategorierna miljö, teknik, ekonomi och hälsa valdes utifrån de Globala målen. De tekniker som utvärderades var alkalisk urintorkning, nitrifikations-destillering och jonbyte där struvitutfällning tillämpades som förbehandling. För den alkaliska urintorkningen tillförs färsk urin till ett alkaliskt medium, för att förhindra kväveförluster, och torkas sedan. I nitrifikations-destillerings tekniken behandlas lagrat urin genom att det först stabiliseras genom en partiell nitrifikation för att sedan destilleras för att reducera volymen. För systemet med jonbyte och struvitfällning, fälls först fosfor från lagrat urin ut och sedan utvinns kvävet genom jonbyte. Urinkoncentreringsteknikerna antogs anläggas i semi-centraliserade reningsverk i källare i bostadsområdet. Övrigt hushållsvatten antogs renas i det lokala avloppsreningsverket. Resultatet visade att samtliga av de tre teknikerna för urinkoncentrering kan bidra till en betydande ökning kväveåtervinning från hushållsavloppet. Dock kan detta komma på bekostnad av ökade årliga kostnader för de boende i området. Innan det är möjligt att avgöra om urinkoncentrering kan vara ett alternativ som ett komplement till den befintliga avloppsreningen i Sege Park krävs vidare studier av urinkoncentreringsteknikerna och deras hållbarhet. Däremot visade denna studie att urinkoncentreringsteknikerna presterar bra i många av de undersökta hållbarhetskriterierna och har därför potential att bidra till de Globala målen, främst när det gäller kväveåtervinning. Denna studie kan därför vara ett incitament för vidare studier som behandlar hållbarheten av en implementering av urinkoncentrering i Sverige.
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3

McMillan, Duncan George Glenn, and n/a. "Proton and iron capture mechanisms of Bacillus sp. strain TA2.A1 at alkaline pH values." University of Otago. Department of Microbiology & Immunology, 2008. http://adt.otago.ac.nz./public/adt-NZDU20081104.090840.

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The thermoalkaliphilic Bacillus sp. strain TA2.A1 was able to grow in pH-controlled batch culture containing a fermentable growth substrate (i.e. sucrose) from pH 7.5 to 10.0 with no significant change in specific growth rate, suggesting that this bacterium is a facultative alkaliphile. However, when strain TA2.A1 was grown on non-fermentable carbon sources like succinate, no growth was observed until the external pH was > 9.0, suggesting this bacterium is an obligate alkaliphile. Growth on succinate at pH 9.5 was sensitive to both carbonyl cyanide m-chlorophenylhydrazone (CCCP) and monensin revealing that both the proton and sodium motive force ([Delta][mu][H⁺] and [Delta][mu][Na⁺], respectively) were obligate requirements for growth at alkaline pH values. Transport of succinate was driven by a chemical gradient of Na⁺ ([Delta]pNa⁺) that was strictly coupled to [Delta][Psi]. A single transport system was detected for the uptake of succinate, with an apparent K[m] of 19 [mu]M and V[max] of 0.45 nmol succinate/min/mg protein. Succinate transport was pH-dependent, and showed optimal activity at pH values greater than 8.5. Other C₄-dicarboxylates (e.g. malate, fumarate) inhibited the uptake of succinate suggesting that the permease was general for other C₄-dicarboxylates. Cytochrome content, succinate dehydrogenase oxidoreductase, and F₁F₀-ATPase activities were lower in membranes from strain TA2.A1 cells grown at pH 7.5 compared to those cultured at 9.5. These data suggest that oxidative phosphorylation-linked processes are down-regulated at neutral pH values, an observation that mirrored oxygen consumption profiles of strain TA2.A1 in whole cells. To study this phenomenon at a molecular level, we measured ATP synthesis by the F₁F₀-ATP synthase from strain TA2.A1 as a function of pH. The strain TA2.A1 F₁F₀-ATP synthase had a pH optimum for ATP synthesis of 9.0-9.5, and significantly lower rates of ATP synthesis observed below pH 9.0. Analysis of the atp operon from the thermoalkaliphilic Bacillus sp. strain TA2.A1 and comparison with other atp operons from alkaliphilic bacteria reveals the presence of a conserved lysine residue at position 180 (Bacillus sp. strain TA2.A1 numbering) within the a subunit of these F₁F₀-ATP synthases. We hypothesize that the basic nature of this residue is ideally suited to capture protons from the bulk phase at high pH. To test this hypothesis, a heterologous expression system for the ATP synthase from Bacillus sp. TA2.A1 (TA2F₁F₀) was developed in Escherichia coli DK8 ([Delta]atp). Amino acid substitutions were made in the a subunit of TA2F₁F₀ at position 180. Lysine (aK180) was substituted for the basic residues histidine (aK180H) or arginine (aK180R), and the uncharged residue glycine (aK180G). ATP synthesis experiments were performed in ADP plus P[i]-loaded right-side out membrane vesicles energized by ascorbate-phenazine methosulfate. When these enzyme complexes were examined for their ability to perform ATP synthesis over the pH range from 7.0 to 10.0, TA2F₁F₀ and aK180R showed a similar pH profile having optimum ATP synthesis rates at pH 9.0 to 9.5 with no measurable ATP synthesis at pH 7.5. Conversely, aK180H and aK180G showed maximal ATP synthesis at pH�s 8.0 and 7.5, respectively. ATP synthesis under these conditions for all enzyme forms was sensitive to DCCD. These data strongly imply that amino acid residue K180 is a specific adaptation within the a subunit of TA2F₁F₀ to facilitate proton capture at high pH. At pH values near the pK[a] of K180, the trapped protons readily dissociate to reach the subunit c binding sites but this dissociation is impeded at neutral pH values causing either a blocking of the proposed H⁺ channel and/or mechanism of proton translocation, and hence ATP synthesis is inhibited. The mechanisms where by alkaliphilic bacteria obtain iron remains unknown. Growth of strain TA2.A1 at pH 9.5 in the presence of the artificial iron chelators ethylenediamine O-hydroxyphenylacetic acid (EDDHA) and 2�2� dipyridal revealed that iron is an important requirement for aerobic growth at alkaline pH values. Furthermore, biochemical analysis showed that Bacillus alcalophilus and Bacillus pseudofirmus both synthesized orange catecholate siderophores, whilst Bacillus halodurans synthesized a hydroxamate siderophore. These tests showed that strain TA2.A1 synthesized both orange catecholate and hydroxamate siderophore/s. Attempts to purify the catecholate were unsuccessful. No homologues of previously identified non-ribosomal peptide synthase (NRPS) genes in Bacillus subtilis and B.halodurans were detected in the genome of strain TA2.A1 using both PCR and Southern hybridization using known non-ribosomal peptide synthase genes.
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4

Falahati, Hamid. "The Characterization of Bimodal Droplet Size Distributions in the Ultrafiltration of Highly Concentrated Emulsions Applied to the Production of Biodiesel." Thesis, University of Ottawa (Canada), 2010. http://hdl.handle.net/10393/19585.

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A non-reactive model system comprising a highly concentrated and unstable oil-in-water emulsion was used to investigate the retention of oil by the membrane in producing biodiesel with a membrane reactor. Critical flux was identified using the relationship between the permeate flux and transmembrane pressure along with the separation efficiency of the membrane. It was shown that separation efficiencies above 99.5% could be obtained at all operating conditions up to the critical flux. It was observed that the concentration of oil in all collected permeate samples using the oil-water system was below 0.2 wt% when operating at a flux below the critical flux. Studies to date have been limited to the characterization of low concentrated emulsions below 15 vol.%. The average oil droplet size in highly concentrated emulsions was measured as 3200 nm employing direct light scattering (DLS) measurement methods. It was observed that the estimated cake layer thickness of 20 to 80 mm was larger than external diameter of the membrane tube i.e. 6 mm based on a large particle size. Settling of the concentrated emulsion permitted the detection of a smaller particle size distribution (30-100 nm) within the larger particles averaging 3200 nm. It was identified that DLS methods could not efficiently give the droplet size distribution of the oil in the emulsion since large particles interfered with the detection of smaller particles. The content of the smaller particles represented 1% of the total weight of oil at 30°C and 5% at 70°C. This was too low to be detected using DLS measurements but was sufficient to affect ultrafiltration. In order to study the critical flux in the presence of transesterification reaction and the effect of cross flow velocity on separation, various oils were transesterified in another membrane reactor providing higher cross flow velocity. higher cross flow velocity provides better separation by reducing materials deposition on the surface of the membrane due to higher shearing. The oils tested were canola, corn, sunflower and unrefined soy oils (Free Fatty Acids (FFA< 1%)), and waste cooking oil (FFA= 9%). The quality of all biodiesel samples was studied in terms of glycerine, mono-glyceride, di-glyceride and tri-glyceride concentrations. The composition of all biodiesel samples were in the range required by ASTM D6751 and EN 14214 standards. A critical flux based on operating pressure in the reactor was reached for waste cooking and pre-treated corn oils. It was identified that the reaction residence time in the reactor was an extremely important design parameter affecting the operating pressure in the reactor.<br>Natural Sciences and Engineering Research Council of Canada (NSERC)
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5

Spelling, Victor, Mathias Axelsson, Lovisa Ringström, af Rosenschöld Johanna Munck, and Anton Lindblad. "Mapping the intrinsic viscosityof hyaluronic acid at high concentrations of OH-." Thesis, Uppsala universitet, Institutionen för teknikvetenskaper, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-325348.

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Hyaluronic acid is commonly used in dermatological fillers in the form of gels. It is established how these gels' firmness is affected by the amount of cross linker and hyaluronic acid respectively. However, the effect of hydroxide ions in solution is rather unknown. This thesis examines how the alkalinity of the solvent affects the intrinsic viscosity of 3 MDa hyaluronic acid by using the method of Ubbelohde capillary viscometry. Sodium hydroxide solutions between 2 and 10 wt% were prepared to study the variation in intrinsic viscosity at concentrations relevant for cross linking (1&lt;wt%). From these respective solutions, four solutions of different mass concentrations of hyaluronic acid were made. The flow time of respective samples were measured between two points in the capillary viscometer in a controlled temperature of 25 °C with an SI Viscoclock to ensure a high accuracy.From the resulting flow times, the intrinsic viscosity was calculated. The intrinsic viscosity varied between 0,55 and 0,70. The relation between intrinsic viscosity and hydroxide ion concentration had a correlation coefficient r &lt; 0,001. No trend could be ensured as the confidence interval for the intrinsic viscosity at the different concentrations was too large.
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6

Morgan, Dana Lee. "Alkaline hydrothermal treatment of titanate nanostructures." Thesis, Queensland University of Technology, 2010. https://eprints.qut.edu.au/39298/1/Dana_Morgan_Thesis.pdf.

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Since its initial proposal in 1998, alkaline hydrothermal processing has rapidly become an established technology for the production of titanate nanostructures. This simple, highly reproducible process has gained a strong research following since its conception. However, complete understanding and elucidation of nanostructure phase and formation have not yet been achieved. Without fully understanding phase, formation, and other important competing effects of the synthesis parameters on the final structure, the maximum potential of these nanostructures cannot be obtained. Therefore this study examined the influence of synthesis parameters on the formation of titanate nanostructures produced by alkaline hydrothermal treatment. The parameters included alkaline concentration, hydrothermal temperature, the precursor material‘s crystallite size and also the phase of the titanium dioxide precursor (TiO2, or titania). The nanostructure‘s phase and morphology was analysed using X-ray diffraction (XRD), Raman spectroscopy and transmission electron microscopy. X-ray photoelectron spectroscopy (XPS), dynamic light scattering (non-invasive backscattering), nitrogen sorption, and Rietveld analysis were used to determine phase, for particle sizing, surface area determinations, and establishing phase concentrations, respectively. This project rigorously examined the effect of alkaline concentration and hydrothermal temperature on three commercially sourced and two self-prepared TiO2 powders. These precursors consisted of both pure- or mixed-phase anatase and rutile polymorphs, and were selected to cover a range of phase concentrations and crystallite sizes. Typically, these precursors were treated with 5–10 M sodium hydroxide (NaOH) solutions at temperatures between 100–220 °C. Both nanotube and nanoribbon morphologies could be produced depending on the combination of these hydrothermal conditions. Both titania and titanate phases are comprised of TiO6 units which are assembled in different combinations. The arrangement of these atoms affects the binding energy between the Ti–O bonds. Raman spectroscopy and XPS were therefore employed in a preliminary study of phase determination for these materials. The change in binding energy from a titania to a titanate binding energy was investigated in this study, and the transformation of titania precursor into nanotubes and titanate nanoribbons was directly observed by these methods. Evaluation of the Raman and XPS results indicated a strengthening in the binding energies of both the Ti (2p3/2) and O (1s) bands which correlated to an increase in strength and decrease in resolution of the characteristic nanotube doublet observed between 320 and 220 cm.1 in the Raman spectra of these products. The effect of phase and crystallite size on nanotube formation was examined over a series of temperatures (100.200 �‹C in 20 �‹C increments) at a set alkaline concentration (7.5 M NaOH). These parameters were investigated by employing both pure- and mixed- phase precursors of anatase and rutile. This study indicated that both the crystallite size and phase affect nanotube formation, with rutile requiring a greater driving force (essentially �\harsher. hydrothermal conditions) than anatase to form nanotubes, where larger crystallites forms of the precursor also appeared to impede nanotube formation slightly. These parameters were further examined in later studies. The influence of alkaline concentration and hydrothermal temperature were systematically examined for the transformation of Degussa P25 into nanotubes and nanoribbons, and exact conditions for nanostructure synthesis were determined. Correlation of these data sets resulted in the construction of a morphological phase diagram, which is an effective reference for nanostructure formation. This morphological phase diagram effectively provides a .recipe book�e for the formation of titanate nanostructures. Morphological phase diagrams were also constructed for larger, near phase-pure anatase and rutile precursors, to further investigate the influence of hydrothermal reaction parameters on the formation of titanate nanotubes and nanoribbons. The effects of alkaline concentration, hydrothermal temperature, crystallite phase and size are observed when the three morphological phase diagrams are compared. Through the analysis of these results it was determined that alkaline concentration and hydrothermal temperature affect nanotube and nanoribbon formation independently through a complex relationship, where nanotubes are primarily affected by temperature, whilst nanoribbons are strongly influenced by alkaline concentration. Crystallite size and phase also affected the nanostructure formation. Smaller precursor crystallites formed nanostructures at reduced hydrothermal temperature, and rutile displayed a slower rate of precursor consumption compared to anatase, with incomplete conversion observed for most hydrothermal conditions. The incomplete conversion of rutile into nanotubes was examined in detail in the final study. This study selectively examined the kinetics of precursor dissolution in order to understand why rutile incompletely converted. This was achieved by selecting a single hydrothermal condition (9 M NaOH, 160 °C) where nanotubes are known to form from both anatase and rutile, where the synthesis was quenched after 2, 4, 8, 16 and 32 hours. The influence of precursor phase on nanostructure formation was explicitly determined to be due to different dissolution kinetics; where anatase exhibited zero-order dissolution and rutile second-order. This difference in kinetic order cannot be simply explained by the variation in crystallite size, as the inherent surface areas of the two precursors were determined to have first-order relationships with time. Therefore, the crystallite size (and inherent surface area) does not affect the overall kinetic order of dissolution; rather, it determines the rate of reaction. Finally, nanostructure formation was found to be controlled by the availability of dissolved titanium (Ti4+) species in solution, which is mediated by the dissolution kinetics of the precursor.
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Albina, Pierre. "Bioréactivité des nitrates en contexte de stockage de déchets radioactifs profond." Thesis, Toulouse 3, 2019. http://www.theses.fr/2019TOU30286.

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En France, il est envisagé de stocker en couche géologique profonde les déchets radioactifs de moyenne activité à vie longue (MAVL). Ces déchets sont chargés en sels de nitrates et après des milliers d'années, le relâchement des nitrates pourrait favoriser la mobilité des radionucléides hors des déchets. Cependant, en présence de matière organique ou d'hydrogène, l'activité bactérienne peut théoriquement réduire les nitrates en espèces azotées plus réduites via la dénitrification. Le 1er objectif de cette thèse est d'évaluer la capacité des bactéries à s'adapter aux conditions physico-chimiques à proximité des déchets, c'est à dire en absence d'oxygène, à pH alcalin entre 9 et 13, en présence de concentrations élevées en nitrates, en présence d'un donneur d'électrons organique (acétate) ou minéral (hydrogène) et en présence de ciment et d'acier solides. Le 2nd objectif est d'évaluer les cinétiques de réduction des nitrates dans les conditions précédemment décrites. La réduction bactérienne des nitrates a été observée jusqu'à pH 11 et 400 mM de nitrates en présence d'acétate et jusqu'à pH 10.5 et 150 mM de nitrates en présence d'hydrogène. En présence d'hydrogène les cinétiques de réduction des nitrates étaient globalement plus ralenties et les bactéries étaient plus sensibles aux pH alcalins que les bactéries qui se développent en présence d'acétate. Ceci s'explique par le fait que l'hydrogène a une solubilité limitée à pression atmosphérique, que l'assimilation de carbone minéral est énergétiquement coûteuse pour les bactéries et enfin qu'en présence d'hydrogène le pH s'élève au cours de l'avancement de la dénitrification. En présence d'acétate le pH s'équilibre autour de 10 grâce aux CO2 produit par l'oxydation de l'acétate. Enfin la présence de ciment solide n'a pas eu de répercussion importante sur l'activité bactérienne, en revanche l'acier solide a stimulé de façon conséquente la réduction des nitrates<br>France has the project to dispose long-lived intermediate-level radioactive waste (ILW-LL) in a deep geological repository. The radioactive waste is loaded with nitrate salts and after thousands of years, the release of nitrates could promote the mobility of radionuclides out of the waste. However, in the presence of organic matter or hydrogen, bacterial activity can theoretically reduce nitrate to smaller nitrogen species through denitrification. The first objective of this thesis is to evaluate the ability of bacteria to adapt to the environment near the waste, i.e. in the absence of oxygen, at alkaline pH between 9 and 13, in the presence of high nitrate concentrations, in the presence of an organic (acetate) or mineral (hydrogen) electrons donor and in the presence of solid cement and solid steel. The second objective is to quantify nitrate reduction kinetics under the conditions described above. Bacterial reduction of nitrates was observed up to pH 11 and 400 mM of nitrates in the presence of acetate and up to pH 10.5 and 150 mM of nitrates in the presence of hydrogen. In the presence of hydrogen, nitrate reduction kinetics were generally slower and bacteria were more sensitive to alkaline pH than heterotrophic bacteria using acetate. This is a consequence of the low solubility of hydrogen, the mineral carbon assimilation expense for bacteria and the alkalinisation during denitrification in the presence of hydrogen. In the presence of acetate the pH equilibrate toward 10, due to CO2 generation when acetate is oxidized. Finally, while the presence of solid cement did not have a significant impact on bacterial activity, solid steel stimulated the reduction of nitrates
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Vikuk, Veronika [Verfasser], Jochen [Gutachter] Krauss, and Jana [Gutachter] Petermann. "Epichloë endophyte-grass symbioses in Germany – Infection rates, alkaloid concentrations and possible intoxication risks / Veronika Vikuk ; Gutachter: Jochen Krauss, Jana Petermann." Würzburg : Universität Würzburg, 2020. http://d-nb.info/122063414X/34.

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Faber, Richard James. "Vegetative growth and alkaloid concentration of Sceletium Tortuosum (L.) N.E. Br. in response to different soilless growing media and fertigation regimes in hydroponics." Thesis, Cape Peninsula University of Technology, 2019. http://hdl.handle.net/20.500.11838/3108.

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Thesis (Master of Horticultural Science)--Cape Peninsula University of Technology, 2019<br>The purpose for this study was to investigate whether Sceletium tortuosum was suitable for cultivation in hydroponics and to determine whether different soilless media and fertigation regimes would have an effect on the vegetative growth and alkaloid concentration of the plant. The experiment was conducted over a period of 6 weeks. Three hundred plants were cultivated from one initial mother plant obtained from Verve Dynamics (Pty) Ltd, Somerset West. Twenty treatments were evaluated with 15 sample replicates. Treatments were made up of 4 different soilless growing media, namely: pure silica sand (SS), 50% silica sand with 50% coco-peat (SC), 50% silica sand with 50% vermiculite (SV), and 50% silica sand with 50% perlite (SP). These growing media were tested in conjunction with 5 different fertigation regimes (FR), plants treated with fertigation regime 1 (FR1) received aqueous nutrient solution once every week, fertigation regime 2 (FR2) received aqueous nutrient solution once every second week, fertigation regime 3 (FR3) received aqueous nutrient solution once every third week, fertigation regime 4 (FR4) received aqueous nutrient solution once every fourth week and fertigation regime 5 (FR5) received aqueous nutrient solution once every fifth week respectively. Chapter 2 reviewed the importance of S. tortuosum and its viability as a Traditional African Medicinal Plant. It was found that S. tortuosum has clear pharmaceutical and economical importance and is one of the only known plants to contain the alkaloids mesembrenone and mesembrine which can be utilized for the promotion of health and treating a variety of psychological disorders such as anxiety and depression. In chapter 3 it was seen that the various treatments had significant effects in terms of plant root growth, shoot growth and dry weight. Treatment SCFR3 showed the highest individual mean value for root growth, while the average from treatments SVFR1-5 displayed the highest average value. The lowest individual value for root growth was observed in treatment SPFR5. Overall treatments with fertigation regime FR3 had better root growth, while fertigation regimes FR5 showed sub-optimal root growth. For shoot growth the highest individual mean value was found in treatment SVFR1, while the highest average value was observed in treatments SCFR1-5. In chapter 4 treatments also had a significant effect on alkaloid concentrations. It was observed that shoot extracts contained a higher concentration of total alkaloids than root extracts, however root extracts had an overall higher amount of delta 7 mesembrenone, and mesembrenone in terms of area %, while shoots had higher amounts of mesembrine. Further the mesembrine standard as mentioned in 4.4.5, shoots clearly have an overall higher concentration of mesembrine than roots. These results suggest that roots of S. tortuosum should be harvested for the purpose of extracting delta 7 mesembrenone and mesembrenone molecules, while the shoots should be harvested for extracting mesembrine. Chapter 5 further investigated the interaction between the vegetative growth and alkaloid concentration of S. tortuosum. There appears to be a clear trend that displays higher concentrations of mesembrine where shoot growth was more optimal, however more optimal growth did not display a higher concentration of total alkaloids. In terms of root growth and total alkaloid concentration, it did not appear that more optimal growth induced higher concentrations of total root alkaloids, meaning reasonable stress on plant root and shoot growth could possibly promote higher concentrations of total alkaloids. It is also clear that overall roots contain more delta 7 mesembrenone and mesembrenone than shoots, suggesting roots should be harvest for extracting these molecules specifically. In most cases high results of delta 7 mesembrenone in roots also had similar amounts of mesembrenone, however certain treatments resulted in higher concentrations of the former and the latter, therefore their similar molecular structure does not always permit similar manifestation in the plant material. Overall this study has found that S. tortuosum is suitable for cultivation in hydroponics, and that soilless media, fertigation regimes as well as soilless media in conjunction with fertigation regimes affected the vegetative growth and alkaloid concentration of S. tortuosum. This research has shown that some soilless media and fertigation regime treatments had more desirable results in terms of vegetative growth and/or alkaloid concentration of the plant.
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Black, Kathleen Scarlett. "EFFECTS OF FESCUE HERBICIDES PLATEAU® AND CIMARRON® ON PREGNANCY MAINTENANCE IN BROODMARES AND ON ALKALOID CONCENTRATIONS IN ENDOPHYTE INFECTED TALL FESCUE." UKnowledge, 2008. http://uknowledge.uky.edu/gradschool_theses/540.

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Ingestion of endophyte infected (E+) fescue by pregnant mares can cause significant reproductive problems. Plateau® and Cimarron® herbicides suppress fescue while leaving desired forages unharmed. To determine if these herbicides are harmful to pregnant mares, they were allowed to graze pastures treated with Plateau®, Cimarron®, or vehicle carrier. Pregnancies were monitored via ultrasonography, blood chemistry, and hematology. Of the components measured only creatinine differed among treatments over time (P=0.0003) and that increase was only significant in one of four studies. Two additional experiments were conducted to determine the effect of the herbicides on alkaloids within E+ fescue. A greenhouse experiment utilizing 52 pots of E+ fescue treated with Plateau®, Cimarron®, or nothing was inconclusive, as some alkaloids increased while others decreased. These results indicated that UV light may be required for normal plant death. In a field experiment 12 plots of mixed vegetation were sprayed with the same treatments, and herbicides decreased ergovaline, N-formylloline, and lysergic acid content (P=0.0460, P=0.0324, P=0.0093 respectively). In conclusion, the herbicides did not alter blood components outside physiological norms, but the alkaloids were still present in dying E+ fescue. It may be safest to remove late gestation mares until E+ fescue is completely decayed.
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11

Johansen, Jonathan Frederick. "Mathematical modelling of primary alkaline batteries." Thesis, Queensland University of Technology, 2007. https://eprints.qut.edu.au/16412/1/Jonathan_Johansen_Thesis.pdf.

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Three mathematical models, two of primary alkaline battery cathode discharge, and one of primary alkaline battery discharge, are developed, presented, solved and investigated in this thesis. The primary aim of this work is to improve our understanding of the complex, interrelated and nonlinear processes that occur within primary alkaline batteries during discharge. We use perturbation techniques and Laplace transforms to analyse and simplify an existing model of primary alkaline battery cathode under galvanostatic discharge. The process highlights key phenomena, and removes those phenomena that have very little effect on discharge from the model. We find that electrolyte variation within Electrolytic Manganese Dioxide (EMD) particles is negligible, but proton diffusion within EMD crystals is important. The simplification process results in a significant reduction in the number of model equations, and greatly decreases the computational overhead of the numerical simulation software. In addition, the model results based on this simplified framework compare well with available experimental data. The second model of the primary alkaline battery cathode discharge simulates step potential electrochemical spectroscopy discharges, and is used to improve our understanding of the multi-reaction nature of the reduction of EMD. We find that a single-reaction framework is able to simulate multi-reaction behaviour through the use of a nonlinear ion-ion interaction term. The third model simulates the full primary alkaline battery system, and accounts for the precipitation of zinc oxide within the separator (and other regions), and subsequent internal short circuit through this phase. It was found that an internal short circuit is created at the beginning of discharge, and this self-discharge may be exacerbated by discharging the cell intermittently. We find that using a thicker separator paper is a very effective way of minimising self-discharge behaviour. The equations describing the three models are solved numerically in MATLABR, using three pieces of numerical simulation software. They provide a flexible and powerful set of primary alkaline battery discharge prediction tools, that leverage the simplified model framework, allowing them to be easily run on a desktop PC.
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12

Johansen, Jonathan Frederick. "Mathematical modelling of primary alkaline batteries." Queensland University of Technology, 2007. http://eprints.qut.edu.au/16412/.

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Three mathematical models, two of primary alkaline battery cathode discharge, and one of primary alkaline battery discharge, are developed, presented, solved and investigated in this thesis. The primary aim of this work is to improve our understanding of the complex, interrelated and nonlinear processes that occur within primary alkaline batteries during discharge. We use perturbation techniques and Laplace transforms to analyse and simplify an existing model of primary alkaline battery cathode under galvanostatic discharge. The process highlights key phenomena, and removes those phenomena that have very little effect on discharge from the model. We find that electrolyte variation within Electrolytic Manganese Dioxide (EMD) particles is negligible, but proton diffusion within EMD crystals is important. The simplification process results in a significant reduction in the number of model equations, and greatly decreases the computational overhead of the numerical simulation software. In addition, the model results based on this simplified framework compare well with available experimental data. The second model of the primary alkaline battery cathode discharge simulates step potential electrochemical spectroscopy discharges, and is used to improve our understanding of the multi-reaction nature of the reduction of EMD. We find that a single-reaction framework is able to simulate multi-reaction behaviour through the use of a nonlinear ion-ion interaction term. The third model simulates the full primary alkaline battery system, and accounts for the precipitation of zinc oxide within the separator (and other regions), and subsequent internal short circuit through this phase. It was found that an internal short circuit is created at the beginning of discharge, and this self-discharge may be exacerbated by discharging the cell intermittently. We find that using a thicker separator paper is a very effective way of minimising self-discharge behaviour. The equations describing the three models are solved numerically in MATLABR, using three pieces of numerical simulation software. They provide a flexible and powerful set of primary alkaline battery discharge prediction tools, that leverage the simplified model framework, allowing them to be easily run on a desktop PC.
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13

El, Moujahid Chaouki. "Propriétés physico-chimiques de systèmes aqueux de tensioactifs non ioniques fluorés." Nancy 1, 1993. http://www.theses.fr/1993NAN10009.

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Ce travail a porté sur une étude physico-chimique de trois séries de tensioactifs fluores non ioniques: c#mf#2#m+#lch#2(oc#2h#4)#noh, hc#mf#2#mch#2(oc#2h#4)#4oh et c#mf#2#m#+#lch#2c(o)n (c#2h#4o)ch#3#2. Les phases lamellaires des systèmes fluorés dans l'eau sont beaucoup plus stables que celles des systèmes hydrogénés. La substitution d'un atome de fluor terminal de la chaine hydrophobe par un atome d'hydrogène limite la solubilité de ces tensioactifs dans l'eau. Au point de vue nicellisation cette substitution correspond à une diminution du nombre de cf#2 d'un motif. La présence de 10 carbones fluorés dans la chaine hydrophobe provoque la formation de phases gels dans l'eau. D'une façon générale, l'étude structurale détaillée a montré que l'épaisseur des chaines fluorées dans les phases lamellaires correspond au 2/3 de celle d'une chaine étirée. Dans la phase lamellaire le volume molaire partiel des tensio-actifs dans l'eau ne se contracte que de 2% par rapport aux tensioactifs purs. Par ailleurs la mesure de viscosité des tensioactifs dans l'eau montre qu'au voisinage d'un point de trouble de 1% les micelles sont allongées tandis qu'elles sont globulaires au voisinage d'un point de trouble de 10%
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14

Cheng, Chun-yee. "Modelling potentials, concentrations and current densities in three-dimensional electrodes for recovery of lead (II) ions from aqueous alkaline solutions by simultaneous electrodeposition of lead and lead dioxide." Thesis, Imperial College London, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.436320.

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15

Hajhassan, Houssein. "Synthese et etude de la structure et de proprietes de lipopeptides amphipatiques." Orléans, 1987. http://www.theses.fr/1987ORLE2007.

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Des lipopeptides amphipathes ont ete synthetises : suivant la methode utilisee. On obtient des lipsamino-acides ou des lipopeptides ; etude par diffraction x, proprietes tensio-actives, pouvoir emulsifiant. Par le test d'hemolyse, il a ete montre que certains lipopeptides ont une hemocompatibilite similaire a celles des meilleurs tensio-actifs bicatenaires
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16

Bayle, Corinne. "Mise au point d'une méthode d'éthérification sélective en série osidique : étude par résonance magnétique nucléaire des molécules amphiphiles synthétisées." Université Joseph Fourier (Grenoble), 1994. http://www.theses.fr/1994GRE10139.

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L'objectif de cette these est la mise au point d'une methode d'etherification en serie osidique et l'etude des proprietes des molecules amphiphiles ainsi synthetisees. La methode d'etherification proposee est une methode indirecte qui se deroule en deux etapes: une iodation selective des positions primaires des derives osidiques est effectuee et les derives iodes obtenus sont alkyles a l'aide d'un hypochlorite d'alkyle. Cette methode nous a permis de synthetiser differents ethers osidiques tels que les methyl 6-o-methyl-, 6-o-ethyl-, 6-o-hexyl-, 6-o-octyl-, 6-o-benzyl-a-d-glucopyranoside. Toutes ces molecules sont obtenues avec de bons rendements (de l'ordre de 75%) et sont caracterisees par resonance magnetique nucleaire du proton et du carbone. Cette methode d'alkylation appliquee aux cyclodextrines a permis de synthetiser les per (6-o-methyl)-a- et -b-cyclodextrines avec de bons rendements (environ 70%). Le mecanisme et les limitations de cette methode sont discutes. Les proprietes des derives obtenus ont ensuite ete etudiees. La concentration micellaire critique du methyl 6-o-octyl-a-d-glucopyranoside a ete mesuree (10 mm). En ce qui concerne les cyclodextrines, les proprietes de complexation de la per (6-o-methyl)-b-cyclodextrine avec deux composes modeles hydrophobes (le paranitrophenol et l'anthraquinone 2-sulfonate de sodium) ont ete etudiees par resonance magnetique nucleaire. Afin de mener a bien ces etudes, la sequence 1d-cosy, technique selective de resonance magnetique nucleaire, a ete mise au point. En particulier, nous avons etudie la determination theorique et experimentale d'un des parametres de cette sequence, le delai d efficace, particulierement important dans les sequences 1d selectives. Ces constantes de complexation sont de 500 m#-#1 a 323 k pour le complexe avec le paranitrophenol et de 2000 m#-#1 pour le complexe avec l'anthraquinone 2-sulfonate de sodium
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17

Rivera, Santillan Rosa Elva. "Flottation ionique des cations métalliques par les collecteurs à longue chaîne : Application aux ions BA**(2+) et GA**(3+)." Nancy 1, 1987. http://www.theses.fr/1987NAN10241.

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Récupération du baryum à partir du milieu aqueux par flottation ionique utilisant des alkylbenzène-sulfonates de sodium. Récupération du gallium, par flottation ionique en utilisant des alkylsulfates de sodium en milieu acide, et des collecteurs à fonction oxine en milieu basique
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18

Lin, Tsung-Hsien, and 林宗賢. "Alkaline medium captures high concentration of carbon dioxide and improves the biomass productivity of an alkali-tolerant microalga mutant strain." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/f9jpc8.

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碩士<br>國立交通大學<br>分子醫學與生物工程研究所<br>105<br>Carbon is the fundamental element of the living system, and carbon dioxide (CO2) is the source of carbon for microalgae. Previous studies indicate that the relatively high CO2 concentration with high microalgal biomass productivity. However, it is too expensive to construct gas line in large scale microalgae pond. The microalgae growth can be provided by exhaust gases (flue gases) from industrial plants, which significantly increases the biomass productivity and the CO2 bioavailability for algae, and it is conducive to carbon capture and reduce greenhouse gas emissions. In addition, the CO2 concentration of flue gases is very high (10~30%), a lot of CO2 is too late to be absorbed by water and easy escape into the environment, so the CO2 bioavailability is extremely low. Therefore, it is essential to develop a system that has high efficient absorb CO2 from exhaust gas, then there is no need to lay a large number of gas pipelines, and also can absorb CO2 with culture medium to provide microalgae growth, the system will be effectively applied to large-scale farming microalgae. This study investigates alkaline medium could absorption more CO2 concentration and provides the technique to promote microalgae biomass productivity in large-scale cultivation. Present study enhances the CO2 retaining capacity of microalgae alkaline culture medium by the addition of NaOH. Microalgae absorb carbon source directly from the dissolved CO2 or HCO3- in the culture medium. Our data showed that microalgae culture medium capture 226, 507, 677, 903, 1100, 1214, and 3195 ppm CO2 by addition of 0 (pH 6), 0.005 (pH 7), 0.01 (pH 8), 0.015 (pH 9), 0.02 (pH 10), 0.025 (pH 11), and 0.06 M (pH 12) M NaOH. Moreover, the microalgae were incubated in a different concentrations (0, 0.005, 0.01, 0.0125, 0.02, 0.025, and 0.06 M) NaOH medium, as a result, the higher the concentration of NaOH capture higher concentration of CO2 to improve the biomass productivity (0.29, 0.40, 0.46, 0.48, 0.51, 0.54, and 0.55 g L-1 day-1). In addition, the microalgae grows in a high pH environment for a long time will be inhibited with intermittent CO2 aeration culture in alkaline medium. In order to improve the microalgae biomass productivity in alkaline medium systems, an alkaline-tolerance Chlorella sp. HPT mutant strain was screened by wild-type Chlorella sp. of NTG mutagenesis. Chlorella sp. HPT could grow well in pH 8~11 medium with air aeration and the mutant microalgae had better alkali resistance compared to the original microalgae Chlorella sp. wild type at pH 10. When microalgal cells were cultured in pH 10 medium, the maximum biomass productivity of Chlorella sp. HPT was higher approximately 2-fold than wild-type Chlorella sp. for 7-days cultivation. Then the mutant microalgae Chlorella sp. HPT was used in alkaline culture medium system. At intermittent CO2 aeration for 30 min at 3, 6, 12, and 24 hours the pH of medium was gradually close to 10 and Chlorella sp. HPT also could grow well in these alkaline culture medium, and the biomass productivity was higher than the Chlorella sp. wild type. When Chlorella sp. HPT aerated with 10% CO2 continuously and 10% CO2 intermittently for 30 min at 3 hours interval indoor semi-continuous cultivation with 3-day replacement for a period of 21 days, the average biomass concentration and biomass productivity of Chlorella sp. HPT were 5.08 and 4.35 g L-1, and 0.878 and 0.726 g L-1 day-1, respectively. For a period of 21 days outdoor semi-continuous cultivation with 7-day replacement, the average biomass concentration and average biomass productivity of Chlorella sp. HPT aerated with CO2 continuously and intermittently during the daytime were 2.13 and 1.87 g L-1, and 0.195 and 0.163 g L-1 day-1, respectively. The results demonstrate that a stable growth performance of Chlorella sp. HPT could be achieved for long-term microalgal cultivation indoor 1-L PBR and outdoor 60-L PBR in semi-continuous cultivation.
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19

Chia-Hui, Hsu, and 許嘉慧. "The concentration of alkaline lipase from Acinetobacter radiaresistens by adsorption." Thesis, 1999. http://ndltd.ncl.edu.tw/handle/85278441695647083304.

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碩士<br>國立成功大學<br>化學工程學系<br>87<br>In this present thesis, the recovery of alkaline lipase from Acinetobacter radiaresistens by adsorption was investigated. It was found that the hydrophobic adsorbent of Accurrel MP1000 would not effectively adsorb enzyme under the conditions of weak ionic strength. With Celite 535 as the adsorbent, the concentration and pH of the phosphate buffer might effect the enzyme adsorption. However, the further addition of salts to the phosphate buffer would not improve the enzyme recovery due to the existing ions in the solution. Adding salts to RO water enhance the enzyme adsorption, in which 100 mM (NH4)Cl was found to give the highest lipase activity and protein recovery with 1.65-fold purification. The surface charge of Celite 535 in RO water was found to be negative from the zeta potential measurement. Although salts did effect the zeta potential of Celite 535, no correspondence between the changes of zeta potential and enzyme adsorption was observed. This implied that electrostatic interaction force between Celite 535 and lipase was not the predominate factor during the protein adsorption. Compared to the adsorption, a higher overall protein recovery without purification effects was found when using the precipitation method of adding acetone into the aqueous solution. With the acetone volume percentage higher than 52.4 %, more than 85 % recovery of lipase activity and protein were obtained. Moreover, adding Celite 535 to the precipitation solution would not improve the recovery such that the adsorb just acted as a dispersant and filler.
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20

Huang, Sih-Wei, and 黃思維. "Mercury and Selenium Concentrations in Fishes from the Water Reservoir of a Chlor-alkali Plant in Tainan." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/91009885405995876089.

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碩士<br>國立中山大學<br>海洋生物科技暨資源學系研究所<br>94<br>The objectives of this study were to investigate the difference and interaction of mercury (Hg) and selenium (Se) among fish species and tissues. In addition, by comparing with the detected concentrations in other regions, it would be possible to evaluate the pollution status. In the meanwhile, this study analyzed the edibility of the fish, the interaction between Hg and Se as well as their impacts on fish growth. Ten species of fish, including tenpounder (Elops machnata), fourlined terapon (Pelates quadrilineatus), whipfin silverbiddy (Gerres filamentosus), common ponyfish (Leiognathus equulus), Hamilton''s thryssa (Thryssa hamiltonii), tilapia (Orechromis niloticus), western Pacific gizzard shad (Nematalosa come), large-scaled mullet (Liza macrolepis), flathead mullet (Mugil cephalus) and milkfish (Chanos chanos), and 20 sediment samples were collected from September to October of 2003 at the reservoir adjacent to a chlor-alkali plant, which had been abandoned for 22 years in Tainan City. Total mercury (THg) and organic mercury (OHg) concentrations were determined in fish muscles, livers, kidneys, gonads, gills and sediment samples. Besides, Se concentrations were also analyzed in fish muscles and livers. Concentrations (mg/kg dry wt.) of THg and OHg in sediment were 43.2±23.4(mean±sd) and 0.013±0.008, respectively. THg, OHg and Se concentrations (mg/kg wet wt.) in fish muscles were 0.432±0.360, 0.305±0.206 and 0.126±0.030, similar to the concentrations in other chlor-alkali polluted regions. With the diet habit of Taiwanese, the Hg concentrations of muscles in the seven fish species exceeded the limit of Hg which was allowed to be consumed by humans. THg and OHg concentrations in the fish muscles showed significant species difference. Obviously, the concentrations in carnivorous fishes were higher than those in omnivorous and herbivorous fishes. The OHg concentrations of fish livers and kidneys were highest in carnivorous fishes, but the THg concentrations were higher in omnivorous fishes than in that of carnivorous and herbivorous fishes. Besides, Se concentrations in fish muscles and livers also showed significant species difference, but did not show relation with the feeding habit of fishes. The Hg levels among fish tissues were highest in livers or kidneys, followed by gonads and muscles, lowest in gills. Generally speaking, Se levels were higher in livers than in muscles. The liver THg concentrations of tilapia reached 10 mg/kg wet wt. Their muscle THg concentrations decreased suddenly and maintained at a level about 0.4 mg/kg wet wt. Meanwhile, the liver inorganic Hg and Se concentrations increased with fish weight, while the liver OHg concentrations did not show such a trend but stay at a low level. High Hg concentrations in the fish tissues resulted in adverse effects on fish health. High Hg concentrations in muscles and livers caused heptasomatic index to decrease in western Pacific gizzard shad and milkfish, and condition factor declined in tilipia. Moreover, gonasomatic index remained low while the Hg concentrations of muscles, livers and gonads reached a threshold, which suggested that the growth of those fishes was likely inhibited in Hg polluted environment.
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21

Chiang, Chi-Feng, and 蔣奇峰. "Simultaneous Production and Concentration of an Alkaline Lipase by Semi-continuous Foam-recovery Fermentation." Thesis, 1999. http://ndltd.ncl.edu.tw/handle/17536168886554574228.

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碩士<br>國立成功大學<br>化學工程學系<br>87<br>Acinetobacter radioresistens, a Gram-negative bacterium isolated from wastewater sludge, produces an extracellular lipase with the properties of absorption at air-water interface. In this study, we try recovering foam by semicontinuous foam-recovery fermentation to separate the lipase from the fermentation system to decrease the lipase concentration for keeping the production of lipase, while reaching the goal of raising the total production, separating the lipase and concentrating it. From the investigation, we found the semicontinuous foam-recovery fermentation not only maintains cells produce lipase but also recovers high-activity lipase from fermentor continually. Consequently, it obtains the effect of producing and concentrating lipase at the same time. Additionally, the best condition of semicontinuous foam-recovery fermentation is to add 0.3﹪gum arabic with basic medium in fermentor and feed 5.0﹪gum arabic with 15 fold basic medium .We can get the recovery of lipase above 50﹪.
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22

Gillis, Joseph Daniel. "Monitoring Organic Contaminant Concentrations and Carbon Mineralization in Field Soils Receiving Alkaline-Stabilized Biosolids." 2011. http://hdl.handle.net/10222/14188.

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The application of municipal sewage biosolids to agricultural land is a common practice worldwide. Increasing attention is being directed at the presence of organic contaminants bound to the organic phase during wastewater treatment, which end up in the biosolids. The goal of this study was to investigate the decomposition of an alkaline-stabilized biosolid being used as an agricultural soil amendment containing unknown organic contaminants. A two year field trial and a 120 day laboratory soil incubation using increasing rates (0, 7, 14, 28, and 42 Mg ha-1) of an alkaline-stabilized biosolid (ASB) were set up to monitor biosolid decomposition and concentrations of selected contaminants over time. The seven contaminants selected for monitoring (p-cresol, indole, 4-t-octylphenol, phenanthrene, triclosan, carbamazepine, and benzo[a]pyrene) represent a wide range of physico-chemical properties and fall under several different chemical classes. The decomposition of ASB in soil was examined in the incubation study. Almost half of the CO2-C evolved from ASB amended soils occurred within the first 6 days, indicating that a relatively labile pool of carbon remains in ASB following the sewage treatment process. By day 121, between 71 to 78% of the total carbon added to soil had been evolved as CO2-C. A new model developed during this study to describe carbon mineralization, a first order plus logistic function (FLOG), performed better than other commonly used models. The method chosen to analyze organic contaminants in soil was only able to determine four out of seven compounds reliably, with recoveries greater than 50% for 4-t-octylphenol, phenanthrene, triclosan, and benzo[a]pyrene. In treated soils, only triclosan was able to be detected and quantified. Average triclosan concentration in the incubation study ranged from a high of 143 ng g-1 on day 3 to a low of 26 ng g-1 by day 121, representing an 81% decrease over a roughly 4 month period under idealized conditions. In the field, triclosan concentrations following a Fall biosolids application in Oct. 2008 increased to detectable levels (29 to 47 ng g-1) in all three plots measured in Nov. 2008, which remained elevated (29 to 66 ng g-1) over the winter period in two out of three plots when sampled in May 2009. Following the Spring application in June 2009, measured triclosan concentrations in July 2009 samples from these same two plots were lower than predicted (33 to 48 ng g-1) and eventually decreased to levels below the detection limit by the Oct. 2009 sampling.
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23

Vikuk, Veronika. "Epichloë endophyte-grass symbioses in Germany – Infection rates, alkaloid concentrations and possible intoxication risks." Doctoral thesis, 2020. https://doi.org/10.25972/OPUS-21389.

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Endophytes live in partial symbiosis inside a plant and have been detected in all tested plants. They belong to the group of fungi or bacteria and their ecological function is mostly unknown. The fungal endophytes of the genus Epichloë belong to a special group of endophytes. Epichloë endophytes live symbiotically inside cool season grass species and some of them are able to produce alkaloids toxic to vertebrates and insects. Their symbiosis is seen as mutualistic for the following reasons: the fungus provides the plant herbivore resistance by producing alkaloids, and it increases the plant’s drought tolerance as well as its biomass production. In return, the grass provides the fungus shelter, nutrients and dispersal. Epichloë endophytes are host specific and the ability to produce alkaloids differs between species. In order to estimate intoxication risks in grasslands, it is necessary to detect infection rates of different grass species with Epichloë endophytes, and to determine the genotypes and chemotypes of the Epichloë species as well as the produced alkaloid concentrations. Factors like land-use intensity or season may have an influence on infection rates and alkaloid concentrations. Also, different methodological approaches may lead to different results. In this doctoral thesis my general aim was to evaluate intoxication risks in German grasslands caused by Epichloë endophytes. For that I investigated infection rates of different grass species and the genotypes and chemotypes of their Epichloë endophytes in German grasslands (Chapter II). Furthermore, I compared alkaloid concentrations detected with dry and fresh plant weight and different analytical methods. I also detected possible changes on the influence of season or land-use intensity (Chapter III). Additionally, I examined infections with Epichloë endophytes and alkaloid concentrations in commercially available grass seed mixtures and determined how that influences the intoxication risk of grazing animals in Europe (Chapter IV). It is of agricultural interest to estimate intoxication risks for grazing livestock on German grasslands due to Epichloë infected grass species. Therefore, it is important to investigate which grasses are infected with the Epichloë endophyte, if the endophytes have the ability to produce vertebrate and invertebrate toxic alkaloids and if the alkaloids are indeed produced. I showed that Epichloë festucae var. lolii infecting agriculturally important Lolium perenne lacked the starting gene for ergovaline biosynthesis. Hence, vertebrate toxic ergovaline was not detected in the majority of the collected L. perenne plants. The detection of alkaloid concentrations is an important tool to estimate intoxication risk for vertebrates, but also invertebrates. My studies showed that the usage of dry plant material is crucial to quantify the correct alkaloid concentrations, and that alkaloid concentrations can vary depending on the detection method. Hence, the usage of validated, similar detection methods is important to be able to compare alkaloid concentrations from different studies. Nevertheless, the trends of seasonal changes and the influence of land-use intensity stayed the same, regardless if dry or fresh plant weight was used. Also, alkaloid concentrations were below toxicity thresholds on population level, regardless of the method used. Two commercially available forage grass and two commercially available turf grass seed mixtures were infected with Epichloë endopyhtes and alkaloids were detected. This might contribute to the spreading of Epichloë endopyhtes in Germany, therefore seed mixtures should be tested for Epichloë infections. My results indicate that the intoxication risk is generally low in Germany at the moment, although that might change due to climate change, an increase of monocultural land-use, or the seeding of Epichloë infected grass seeds<br>Endophyten leben, zumindest zeitweise, symbiontisch in Pflanzen und sind bisher in allen untersuchten Pflanzen nachgewiesen worden. Es handelt sich dabei um Pilze oder Bakterien und ihre ökologische Funktion ist meistens unbekannt. Eine spezielle Gruppe der Endophyten sind Pilzendophyten der Gattung Epichloë. Diese leben symbiontisch innerhalb von kaltgemäßigten Grasarten und einige sind in der Lage vertebraten- und/oder insektentoxische Alkaloide herzustellen. Die Symbiose wird meist als mutualistisch bezeichnet, weil der Pilz der Pflanze einen Herbivorenschutz durch die Produktion der Alkaloide und eine gesteigerte Trockenresistenz und Biomassesteigerung bietet. Das Gras hingegen bietet dem Pilz Unterkunft, Nährstoffe und Verbreitung. Epichloë Endophyten sind wirtsspezifisch und die Fähigkeit Alkaloide zu produzieren schwankt zwischen den Arten. Um das Vergiftungsrisiko im Grünland einzuschätzen, ist es nötig Infektionsraten verschiedener Grasarten mit Epichloë Endophyten, die Geno- und Chemotypen der Epichloë Arten, und die produzierten Alkaloidkonzentrationen zu bestimmen. Faktoren wie Landnutzungsintensität oder die Jahreszeit können Infektionsraten und Alkaloidkonzentrationen beeinflussen. Ebenso können Alkaloidkonzentrationen von methodischen Faktoren abhängen. In dieser Doktorarbeit habe ich Infektionsraten verschiedener Grasarten in Deutschland und die Geno- und Chemotypen ihrer Epichloë Endophyten untersucht (Kapitel II). Außerdem habe ich Alkaloidkonzentrationen mit Frisch- bzw. Trockengewicht gemessen und mit verschiedenen analytischen Methoden verglichen, um mögliche Änderungen beim Einfluss von Jahreszeiten oder der Landnutzungsintensität zu detektieren. Des Weiteren habe ich das Vergiftungsrisiko auf deutschen Grasflächen abgeschätzt (Kapitel III). Zusätzlich habe ich kommerziell erhältliche Grassaatgutmischungen auf Epichloë Infektionen und Alkaloidgehalt untersucht und habe versucht einzuschätzen, wie sich das auf das Vergiftungsrisiko von Weidevieh in Europa auswirkt (Kapitel IV). Die Einschätzung von Vergiftungsrisiken für Weidevieh aufgrund von Epichloë infizierten Grasarten auf deutschen Graslandflächen ist von landwirtschaftlichem Interesse. Deshalb ist es wichtig zu untersuchen, welche Grasarten mit Epichloë Endophyten infiziert sind, ob der Endophyt in der Lage ist vertebraten- oder insektentoxische Alkaloide zu produzieren und ob diese tatsächlich produziert werden. Ich konnte zeigen, dass Epichloë festucae var. lolii, welches das landwirtschaflich wichtige Lolium perenne infiziert, das Startgen für die Ergovalinbiosynthese fehlt. Deshalb wurde das vertebraten-toxische Ergovalin in der Mehrheit der gesammelten L. perenne Pflanzen nicht nachgewiesen. Die Detektion von Alkaloidkonzentrationen ist ein wichtiges Werkzeug, um das Vergiftungsrisiko für Vertebraten aber auch Invertebraten einschätzen zu können. Ich konnte zeigen, dass die Verwendung von trockenem Pflanzenmaterial essenziell ist, um korrekte Alkaloidkonzentrationen zu quantifizieren und dass Alkaloidkonzentrationen in Abhängigkeit von der Detektionsmethode schwanken können. Deshalb ist die Verwendung von validierten, ähnlichen Detektionsmethoden wichtig, um die Alkaloidkonzentrationen von verschiedenen Studien vergleichen zu können. Dennoch blieben die jahreszeitlichen Trends und der Einfluss von Landnutzungsintensität gleich, egal ob Trocken- oder Frischgewicht der Pflanze verwendet wurde und Alkaloidkonzentrationen lagen unter der Toxizitätsschwelle auf Populationsebene. Ich konnte außerdem zeigen, dass zwei kommerziell erwerbliche Futtergrasmischungen, sowie zwei Rasengrasmischungen mit Epichloë Endophyten infiziert waren und auch Alkaloide detektiert werden konnten. Das könnte zu einer weiteren Ausbreitung von Epichloë-Endophyten in Deutschland beitragen, weshalb Saatgutmischungen auf Epichloë Infektionen getestet werden sollten. Meine Ergebnisse zeigen, dass das Vergiftungsrisiko in Deutschland im Moment generell eher niedrig ist. Allerdings kann sich das auf Grund von Klimawandel, zunehmenden Monokulturen in der Landnutzung, aber auch der Aussaat von Epichloë infiziertem Saatgut ändern
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Wu, Yao-Wun, and 吳瑤雯. "The influence of drinking alkaline electrolyzed water on uric acid concentration after high intensity interval exercise." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/x9fp6p.

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碩士<br>國立東華大學<br>體育與運動科學系<br>106<br>Purpose:This study aims at exploring the influence of drinking alkaline electrolyzed water on uric acid concentration after high intensity interavl exercise. Methods:Nine healthy university male students were selected to perform high intensity interavl exercise by riding cycle ergometer, and drank alkaline electrolyzed water or pure water after the exercise. The blood samples were collected before the exercise, right after the exercise, and one hour, two hours, twenty-four hours after the exercise. The urine samples were collected before the exercise, right after the exercise, and one hour, two hours after the exercise. Serum uric acid (SUA) , Urine rine acid(UUA), Creatinine(Cre), and Lactate Dehydrogenase(LDH) were examined by biochemical tests. Data were analyzed by SPSS 14.0 nonparametric methods with the statistical significance set at .05 . Conclusions:The effects of drinking alkaline electrolyzed water and pure water were statistically significant( p < .05) on all time points. The highest SUA were found an hour after intensity interavl exercise, and gradually decreased afterwards. There was a decrease in UUA excretion after intensity interavl exercise. Although immediate influences were found on Cre and LDH, they, however, both resumed to normal levels twenty-four hours after the exercise. Our findings also indicated that drinking alkaline electrolyzed water and pure water showed no significant effects ( p > .05) on all physiological data.
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Chang, Jung C., and 張農謙. "Copper Recovery and Treatments of High Concentration Acidic and Alkaline Waste Solutions from Printed Circuit Board Industry." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/77082527238926495747.

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碩士<br>元智大學<br>化學工程學系<br>93<br>Abstract Printed circuit board (PCB) production in Taiwan is currently ranked No. 3 worldwide, next only to the US and Japan. The PCB production is complex involves a number of specialty chemicals and materials, leading to many waste solid and liquid pollutants being discarded. Typical waste liquid solutions of a PCB plant from the etching processes contain high concentrations of many heavy metals, including copper, lead, nickel, etc. Disposal of these etching waste solutions is not easy and is usually done out of site by professional agencies. The purpose of this research is to investigate the feasibility of utilizing the acidic and alkaline etching solutions for copper recovery. Three sets of experimental tests were performed in the present research. The first set was to test the neutralization process using alkaline and acid or acidic solutions. These tests focused on the pH optimization for maximum copper recovery. The test results indicated that very high copper recovery over 98% can be achieved as a solid product. Using ammonium chloride, the residual solution could be properly adjusted for recycle for etching reuse. In the second test set, acidic etching solution was neutralized using sodium hydroxide at various pHs and temperatures. The recovered copper first appeared as copper hydroxide which was then converted copper oxide. In the first test set, the residual solution still contained a significant amount of copper. It could be adjusted for ammonium context for recycle as etching agent. However, in the third test set, attempt was made to further recover the remaining copper in the residual solution by utilizing sodium chloride neutralization. Operating under the conditions of pH 12 and 95oC, the copper content in the residual waste solution could be further reduced from about 2,000 mg/l to below 1 mg/l, enabling discharge standard of the treated waste solution.
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Yang, Yung-hua, and 楊雍華. "The last 100,000 years alkenone-based paleo-SSTs and terregenous n-alkane concentrations of core MD012404 in the Okinawa Trough." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/30462838505739620905.

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碩士<br>國立中山大學<br>海洋地質及化學研究所<br>99<br>In this study, concentrations of organic biomarkers of core MD012404, recovered from central part of the Okinawa Trough, were analyzed, included of unsaturated alkenones and n-alkanes, for reconstructing paleoenviromental and paleoclimatic records for the past 100,000 years. The unsaturated alkenone index of Uk′37 were calculated for reconstructing past variations of sea surface temperature (SST) in the East Chna Sea (ECS). Through the past 100,000 years, our record revealed that the varied pattern of paleo-SSTs of the ECS was mainly reflecting Interglacial/Glacial cycles. This result indicates that the enhanced East Asian winter monsoon which is induced by the changing orbital forcing is the dominant controlling factor to influence the hydrological conditions in the ECS. Otherwise, except of the warming event of Bølling-Allerød and cooling event of Younger Dryas, no obviously cooling trends were observed in the record indicating that the Uk′37 based SST was not sensitive to the millennial-scaled climate events. This may be caused by the slow response of the SST to the millennial-sclaed events. The concentrations of unsaturated alkenones reconstructed in this study can represent to the surface productivity of the ECS. Our record shows that the values are higher in glacial period than in interglacial period. The higher productivity observed in glacial period may result from the wind-driven water mixing. Therefore, the well-mixing of surface and subsurface water thus can supply higher nutrients upto the surface water than induce the higher productivity in glacial period in the ECS. However, a more complicated pattern is found in MIS 5, the unsaturated alkenones have extremely high values in this interval which is different to the Holocene even though that the climatic conditions and global sea level are similar in these two periods. These high values may be caused by either higher surface production or well preservation, which results from the pool ventilation in the ECS. In addition, distributed pattern of n-alkanes can represent to the possible sources of organic materials and vegetation changes on land. Our record shows that n-C31 alkane is dominant in n-alkanes, and the distribution pattern of n-alkanes (C31 > C29 > C33 > C27 > C25 ) is similar to the sediments discovered on the continental shelf of ECS and the estuary of the Changjiang River and is different with the sediments from the Lanyang Hsi River. This fact indicates that the organic materials buried in sediments of the Okinawa Trough are mainly contribute from the ECS continental shelf and the Changjiang River is serves as the main contributor of terrestrial sediments in the study region. Our calculated Carbon preference index (CPI) indicates that terrigenous orangic matters are less influenced by degradation and diagenesis in glacial period, especially during LGM, and the changing pattern is highly correlated with the global sea level changes. Lower sea level observed in glacial period shorten the transporting distance of sediments from the Changjiang River to the Okinawa Trough thus causes more terrestrial inputs and deposits in the Okinawa Trough.
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Yeh, Jih-Chen, and 葉日禎. "Higher serum concentrations of non-hepatic alkaline phosphatase and CRP predict the risk of vertebral fracture in patients with rheumatoid arthritis – a preliminary study." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/qgb26a.

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碩士<br>國立臺灣大學<br>臨床牙醫學研究所<br>105<br>Patients with RA are at high risk for vertebral fractures (VF). Higher serum concentrations of non-hepatic alkaline phosphatase (NHALP) and C-reactive protein (CRP) are associated with disease activity in patients with rheumatoid arthritis (RA). Nonetheless, no epidemiological study in RA patients has been conducted to investigate the interaction and joint effect of NHALP and CRP on VF. We analyzed 507 patients diagnosed with RA (ICD-9 codes: ICD-9-CM codes: 714.0, 714.2, 714.30–714.33 ) from January 2006 to June 2017 from hospital databanks. Unadjusted and adjusted hazard ratios (aHRs) of VF were calculated for different categories of serum NHALP and CRP using the Cox regression model. The modification effect between serum NHALP and CRP on VF was determined using an interaction product term. Higher serum concentrations of NHALP (NHALP>150U/L) and CRP (>3.0mg/dL) were associated with incremental risks of VF (aHR: 1.8 [95% confidence intervals (CIs): 1.1-2.7] and 1.9 [95% CI: 1.3-2.8] compared to the lowest HR category, respectively). The interaction between NHALP and CRP on VF events was statistically significant (p<0.05). In the stratified analysis, patients with combined highest serum NHALP and CRP had the greatest risk (aHR: 3.6 [95% CI: 1.5-7.6]) compared to the lowest HR group (NHALP < 80 U/L and CRP < 1mg/dL). Our study indicates higher serum concentrations of NHALP and CRP are valuable predictors of VF and interact to increase the risk of VF in RA patients. Combined NHALP and CRP could serve as a useful surrogate marker of VF in RA patients.
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