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Mixed metal oxide - noble metal catalysts for total oxidation of volatile organic compounds and carbon monoxideFerrandon, Magali January 2001 (has links)
CO, volatile organic compounds, and polyaromatics areubiquitous air pollutants that give rise to deleterious healthand environmental effects. Such compounds are emitted, forinstance, by the combustion of wood, particularly fromsmall-scale heating appliances. Total catalytic oxidation isconsidered to be an effective approach in controlling theseemissions, however, some problems remain such as thenon-availability of catalysts with low-cost, high activity andstability in prevailing conditions. Hence, this thesis aims atthe development of oxidation catalysts and improvedunderstanding of their behaviour. The catalytic activity was evaluated for the oxidation of amixture of CO, naphthalene (or ethylene), and methane inpresence of carbon dioxide, water, oxygen and nitrogen. Variouscharacterisation techniques, including Temperature-ProgrammedReduction and Oxidation, BET-Surface Area Analysis, X-RayDiffraction, X-Ray Photoelectron Spectroscopy, RamanSpectroscopy and Scanning and Transmission Electron Microscopywere used. In the first part of this thesis, catalysts based on metaloxides (MnOx, CuO) and/or a low amount of noble metals (Pt, Pd)supported on alumina washcoat were selected. It was shown thatPt and Pd possessed a superior catalytic activity to that ofCuO and MnOxfor the oxidation of CO, C10H8and C2H4, while for the oxidation of CH4, CuO was largely more active than noble metals,and MnOxas active as Pd and Pt. Some mixed metaloxide-noble metal catalysts showed decreased activity comparedto that of noble metals, however, a higher noble metal loadingor a successive impregnation with noble metals led to positivesynergetic effects for oxidation. Deactivation of the catalysts by thermal damage and sulphurpoisoning is addressed in the second part of the dissertation.An alumina washcoat was found to be well anchored to themetallic support after thermal treatment at 900°C due tothe growth of alumina whiskers. The sintering of the washcoatwas accelerated after high temperature treatments in thepresence of metal catalysts. In addition, alumina was found toreact with CuO, particularly in presence of noble metals at900°C, to form inactive CuAl2O4. However, MnOxcatalyst benefits from the more active Mn3O4phase at high temperature, which makes it asuitable active catalyst for the difficult oxidation of CH4. Pt sintering was delayed when mixed with CuO,thus giving more thermally resistant catalyst. The mixed metaloxide-noble metal catalysts showed higher activity afterpre-sulphation of the catalysts with 1000 ppm SO2in air at 600°C or during activitymeasurement in presence of 20 ppm SO2in the gas mixture, compared to single componentcatalysts. In some cases, the activities of the mixed catalystswere promoted by pre-sulphation due to the presence of sulphatespecies. Thermal stabilisation of the catalytic componentsand thealumina by promotion of La in the washcoat is discussed in thethird section. The stabilising effect of La at high temperatureis also compared to that of Ce added in the catalysts for otherpurposes. Due to its better dispersion, La contributed to thethermal stabilisation of the alumina washcoat and its activecomponents to a higher extent than Ce did. La provided a betterdispersion and a higher saturation of metal oxides in thealumina support, and at the same time stabilised the activityof the catalysts by preventing undesirable solid-phasereactions between metal oxide and alumina. In addition, La wasfound to enhance the dispersion and the oxygen mobility of CeO2. Cu-Ce interactions were found to promotesubstantially the CO oxidation due to an increase of thestability and reducibility of Cu species. Synergetic effectswere also found between Ce and La in the washcoat of CuO-Ptcatalyst, which facilitated the formation of reduced Pt and CeO2, thus enhancing significantly the catalyticactivity compared to that of a Pt only catalyst. The last part was an attempt to demonstrate the potential ofa catalyst equipped with a pre-heating device in a full-scalewood-fired boiler for minimising the high emissions during thestart-up phase. During the first ten minutes of the burningcycle a significant reduction of CO and hydrocarbons wereachieved. <b>Keywords</b>: wood combustion, catalysts, total oxidation,manganese, copper, platinum, palladium, lanthanum, cerium, CO,VOC, methane, deactivation, thermal stability, sulphurdioxide.
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Mixed metal oxide - noble metal catalysts for total oxidation of volatile organic compounds and carbon monoxideFerrandon, Magali January 2001 (has links)
<p>CO, volatile organic compounds, and polyaromatics areubiquitous air pollutants that give rise to deleterious healthand environmental effects. Such compounds are emitted, forinstance, by the combustion of wood, particularly fromsmall-scale heating appliances. Total catalytic oxidation isconsidered to be an effective approach in controlling theseemissions, however, some problems remain such as thenon-availability of catalysts with low-cost, high activity andstability in prevailing conditions. Hence, this thesis aims atthe development of oxidation catalysts and improvedunderstanding of their behaviour.</p><p>The catalytic activity was evaluated for the oxidation of amixture of CO, naphthalene (or ethylene), and methane inpresence of carbon dioxide, water, oxygen and nitrogen. Variouscharacterisation techniques, including Temperature-ProgrammedReduction and Oxidation, BET-Surface Area Analysis, X-RayDiffraction, X-Ray Photoelectron Spectroscopy, RamanSpectroscopy and Scanning and Transmission Electron Microscopywere used.</p><p>In the first part of this thesis, catalysts based on metaloxides (MnO<sub>x</sub>, CuO) and/or a low amount of noble metals (Pt, Pd)supported on alumina washcoat were selected. It was shown thatPt and Pd possessed a superior catalytic activity to that ofCuO and MnO<sub>x</sub>for the oxidation of CO, C<sub>10</sub>H<sub>8</sub>and C<sub>2</sub>H<sub>4</sub>, while for the oxidation of CH<sub>4</sub>, CuO was largely more active than noble metals,and MnO<sub>x</sub>as active as Pd and Pt. Some mixed metaloxide-noble metal catalysts showed decreased activity comparedto that of noble metals, however, a higher noble metal loadingor a successive impregnation with noble metals led to positivesynergetic effects for oxidation.</p><p>Deactivation of the catalysts by thermal damage and sulphurpoisoning is addressed in the second part of the dissertation.An alumina washcoat was found to be well anchored to themetallic support after thermal treatment at 900°C due tothe growth of alumina whiskers. The sintering of the washcoatwas accelerated after high temperature treatments in thepresence of metal catalysts. In addition, alumina was found toreact with CuO, particularly in presence of noble metals at900°C, to form inactive CuAl<sub>2</sub>O<sub>4</sub>. However, MnO<sub>x</sub>catalyst benefits from the more active Mn<sub>3</sub>O<sub>4</sub>phase at high temperature, which makes it asuitable active catalyst for the difficult oxidation of CH<sub>4</sub>. Pt sintering was delayed when mixed with CuO,thus giving more thermally resistant catalyst. The mixed metaloxide-noble metal catalysts showed higher activity afterpre-sulphation of the catalysts with 1000 ppm SO<sub>2</sub>in air at 600°C or during activitymeasurement in presence of 20 ppm SO<sub>2</sub>in the gas mixture, compared to single componentcatalysts. In some cases, the activities of the mixed catalystswere promoted by pre-sulphation due to the presence of sulphatespecies.</p><p>Thermal stabilisation of the catalytic componentsand thealumina by promotion of La in the washcoat is discussed in thethird section. The stabilising effect of La at high temperatureis also compared to that of Ce added in the catalysts for otherpurposes. Due to its better dispersion, La contributed to thethermal stabilisation of the alumina washcoat and its activecomponents to a higher extent than Ce did. La provided a betterdispersion and a higher saturation of metal oxides in thealumina support, and at the same time stabilised the activityof the catalysts by preventing undesirable solid-phasereactions between metal oxide and alumina. In addition, La wasfound to enhance the dispersion and the oxygen mobility of CeO<sub>2</sub>. Cu-Ce interactions were found to promotesubstantially the CO oxidation due to an increase of thestability and reducibility of Cu species. Synergetic effectswere also found between Ce and La in the washcoat of CuO-Ptcatalyst, which facilitated the formation of reduced Pt and CeO<sub>2</sub>, thus enhancing significantly the catalyticactivity compared to that of a Pt only catalyst.</p><p>The last part was an attempt to demonstrate the potential ofa catalyst equipped with a pre-heating device in a full-scalewood-fired boiler for minimising the high emissions during thestart-up phase. During the first ten minutes of the burningcycle a significant reduction of CO and hydrocarbons wereachieved.</p><p><b>Keywords</b>: wood combustion, catalysts, total oxidation,manganese, copper, platinum, palladium, lanthanum, cerium, CO,VOC, methane, deactivation, thermal stability, sulphurdioxide.</p>
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Influence of SO2 fumigation on growth, photosynthesis, lipoxygenase and peroxidase activities of soybean (Glycine max), in open-top chambers / Susan LindequeLindeque, Susan January 2012 (has links)
Air pollutant exposure poses a health risk to humans and impacts negatively on agriculture. High levels of air pollution resulted in extensive crop damage and yield reduction in Europe and USA. The Highveld region in South Africa, a very important area for maize and soya production, has already been declared an air pollution hot spot, with SO2 being the most concerning air pollutant. Most of the SO2 over the Highveld originates from the burning of coal for power generation. Developing countries, such as South Africa, are highly dependent on agriculture for food security and high levels of air pollution pose serious risks to the agricultural industry. Currently very little information is available on the effects of air pollution on crop production in South Africa.
This study aimed to establish exposure-response relationship for SO2 on soybean and the quantification thereof on the morphological, physiological and biochemical characteristics. Two soybean cultivars were used, namely: LS 6164 and PAN 1666. The plants were fumigated for 7 hours, 7 days a week with 0 (carbon filtered control; CF), 25, 75 and 150 ppb SO2. The effect of SO2 was investigated on the growth, photosynthetic capabilities, photosynthetic gas exchange, peroxidase activity and lipoxygenase activity of the cultivars.
Foliar injuries and interveinal chlorosis were visible with increasing levels of SO2 as well as a decrease in biomass accumulation, especially in root biomass; a more prominent feature of LS 6164. The number of nodules of both cultivars decreased insignificantly as the levels of SO2 increased. The number of pods per plant and the average weight of 30 seeds indicated a downward trend with an increase in SO2 concentration. The chlorophyll content of PAN 1666 was lower compared to LS 6164. PAN 1666 had the largest reduction in stomatal conductance at 150 ppb SO2 fumigation.
The photosynthetic vitality index indicated that LS 6164 was more sensitive to SO2 inhibition from 25 ppb SO2 and higher, whereas PAN 1666 mostly became sensitive to SO2 from 75 ppb SO2. A decrease in the ability to absorb light energy, the trapping of excitation energy to transfer electrons beyond QA-, and the reduction of end electron acceptors all contributed to the decline in the vitality index.
Sulphur content increased significantly in the 75 ppb and 150 ppb treatments of both cultivars. Induced peroxidase and lipoxygenase activity was seen in both cultivars, especially at higher concentrations of SO2 treatments. PAN 1666 had a higher rate of peroxidase and lipoxygenase activity compared to LS 6164.
The implication for SO2 on crop production in the highly industrial Highveld area was demonstrated to be potentially of great concern. The dose-response relationships plotted for OJIP parameters emphasized that SO2 is an inhibitor of photosynthesis and phytotoxic of nature. Both cultivars experienced limitations from 75 ppb, especially at the 150 ppb SO2 concentration. From these results it appears that PAN 1666 is more adapted to SO2 compared to LS 6164 and levels of 75 ppb SO2 and higher become toxic to these plants. / Thesis (Master of Environmental Sciences)--North-West University, Potchefstroom Campus, 2013
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Influence of SO2 fumigation on growth, photosynthesis, lipoxygenase and peroxidase activities of soybean (Glycine max), in open-top chambers / Susan LindequeLindeque, Susan January 2012 (has links)
Air pollutant exposure poses a health risk to humans and impacts negatively on agriculture. High levels of air pollution resulted in extensive crop damage and yield reduction in Europe and USA. The Highveld region in South Africa, a very important area for maize and soya production, has already been declared an air pollution hot spot, with SO2 being the most concerning air pollutant. Most of the SO2 over the Highveld originates from the burning of coal for power generation. Developing countries, such as South Africa, are highly dependent on agriculture for food security and high levels of air pollution pose serious risks to the agricultural industry. Currently very little information is available on the effects of air pollution on crop production in South Africa.
This study aimed to establish exposure-response relationship for SO2 on soybean and the quantification thereof on the morphological, physiological and biochemical characteristics. Two soybean cultivars were used, namely: LS 6164 and PAN 1666. The plants were fumigated for 7 hours, 7 days a week with 0 (carbon filtered control; CF), 25, 75 and 150 ppb SO2. The effect of SO2 was investigated on the growth, photosynthetic capabilities, photosynthetic gas exchange, peroxidase activity and lipoxygenase activity of the cultivars.
Foliar injuries and interveinal chlorosis were visible with increasing levels of SO2 as well as a decrease in biomass accumulation, especially in root biomass; a more prominent feature of LS 6164. The number of nodules of both cultivars decreased insignificantly as the levels of SO2 increased. The number of pods per plant and the average weight of 30 seeds indicated a downward trend with an increase in SO2 concentration. The chlorophyll content of PAN 1666 was lower compared to LS 6164. PAN 1666 had the largest reduction in stomatal conductance at 150 ppb SO2 fumigation.
The photosynthetic vitality index indicated that LS 6164 was more sensitive to SO2 inhibition from 25 ppb SO2 and higher, whereas PAN 1666 mostly became sensitive to SO2 from 75 ppb SO2. A decrease in the ability to absorb light energy, the trapping of excitation energy to transfer electrons beyond QA-, and the reduction of end electron acceptors all contributed to the decline in the vitality index.
Sulphur content increased significantly in the 75 ppb and 150 ppb treatments of both cultivars. Induced peroxidase and lipoxygenase activity was seen in both cultivars, especially at higher concentrations of SO2 treatments. PAN 1666 had a higher rate of peroxidase and lipoxygenase activity compared to LS 6164.
The implication for SO2 on crop production in the highly industrial Highveld area was demonstrated to be potentially of great concern. The dose-response relationships plotted for OJIP parameters emphasized that SO2 is an inhibitor of photosynthesis and phytotoxic of nature. Both cultivars experienced limitations from 75 ppb, especially at the 150 ppb SO2 concentration. From these results it appears that PAN 1666 is more adapted to SO2 compared to LS 6164 and levels of 75 ppb SO2 and higher become toxic to these plants. / Thesis (Master of Environmental Sciences)--North-West University, Potchefstroom Campus, 2013
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Volatile sulfur compounds in coastal acid sulfate soils, northern N.S.W.Kinsela, Andrew Stephen, School of Biological, Earth & Environmental Sciences, UNSW January 2007 (has links)
The cycling of biogenic volatile sulfur compounds (VSCs) within marine and terrestrial ecosystems has been shown to play an integral role in atmospheric chemistry; by influencing global climate change through the creation of cloud condensation nuclei and controlling acid-base chemistry; as well as influencing sediment chemistry including the interactions with trace metals, particularly regarding iron sulfide formation. Despite this, the examination of VSCs within Australian coastal acid sulfate soils (ASS) is an unexplored area of research. As ASS in Australia occupy an area in excess of 9 M ha, there is a clear need for a greater understanding of the cycling of these compounds within such systems. This thesis looks at the concentrations of several VSCs within agricultural and undisturbed ASS on the east coast of Australia. Initial measurements of sulfur dioxide (SO2) were made using passive diffusion samplers, which were followed by two detailed field-based studies looking at the concentrations and fluxes of both SO2 and hydrogen sulfide (H2S) using flux-gradient micrometeorological techniques. These novel results indicated that this agricultural ASS was a substantial source of atmospheric H2S (0.036-0.056 gSm-2yr-1), and SO2 (0.095-0.31 gSm-2yr-1), with flux values equating to many other salt- and freshwater marshes and swamps. The flux data also suggested that the ASS could be a continual source of H2S which is photo-oxidised during the daytime to SO2. Measurements of both compounds showed separate, inverse correlations to temperature and moisture meteorological parameters indicating possible contributing and / or causal release factors. Further identification of these and other VSCs within ASS samplers was undertaken in the laboratory using gas chromatography in combination with solid-phase microextraction. Although SO2 and H2S were not discovered within the headspace samples, two other VSCs important in atmospheric sulfur cycling and trace metal geochemistry were quantified; dimethylsulfide (DMS; > 300??g/L) and ethanethiol (ESH > 4??g/L). The measurements of H2S, DMS and ESH are the first quantifications with Australian ASS, and they may be important for refining regional or local atmospheric sulfur budgets, as well as interpreting previous SO2 emissions from ASS. Ultimately this thesis further enhances our understanding of the cycling of VSCs within acid sulfate systems.
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An evaluation of sulphur dioxide fume levels and the prevalence of darkroom disease symptoms amongst radiology workers in NamibiaDamases, Christine January 2006 (has links)
Thesis (M.Tech.: Radiography)-Dept. of Radiography, Durban University of Technology, 2006
xi, 86 leaves, Annexures A-Q / The study will determine the sulphur dioxide (SO2) levels in the x-ray department and evaluate it’s effects on the health of the radiology workers. The aim of the study is to mainly create awareness of occupational hazards posed by processing chemistry to radiology workers.
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Investigating the impact of sulphur dioxide on Brettanomyces bruxellensis at a molecular and cellular levelDuckitt, Edward 03 1900 (has links)
Thesis (MSc)--Stellenbosch University, 2012. / ENGLISH ABSTRACT: The yeast Brettanomyces was isolated from beer in 1904 and associated with wine thereafter. A
sporulating form, Dekkera, was discovered later. Brettanomyces bruxellensis produces high
levels of volatile phenol off-flavours in wine. Sulphur dioxide (SO2) is the most widely used
chemical preservative in wine. Yeasts have several mechanisms to cope with the SO2, namely
Ssu1p, a membrane bound SO2 transporter; sulphite reduction, sulphite oxidation and
acetaldehyde production. In unfavourable environmental conditions, certain yeasts can enter a
viable-but-non-culturable (VBNC) state which is characterised by reduced metabolic rate,
inability to reproduce on solid media and a reduction of cell size. VBNC can be triggered by
chemical stress such as high SO2 levels. The objectives of this study were to examine the SO2
tolerance of B. bruxellensis and Saccharomyces cerevisiae, to quantify their rates of SO2
accumulation and efflux, determine the effect of SO2 on their energy metabolism and investigate
if B. bruxellensis possesses an orthologue to S. cerevisiae SSU1.
In this study, the identity of a number of Brettanomyces/Dekkera strains was confirmed using
5.8S rDNA-ITS RFLP analysis and DNA sequencing. Sporulation assays were used to confirm
whether these strains belonged to the Dekkera or Brettanomyces genus. A method to
accurately quantify SO2 in laboratory conditions was optimised. Molecular SO2 tolerance was
tested by spotting fresh yeast cultures on media with SO2 and/or ethanol. Tolerance to SO2
and/or ethanol showed highly strain dependent results with S. cerevisiae showing the highest
tolerance levels while B. bruxellensis tolerated SO2 and ethanol poorly but certain strains grew
well with only SO2. The SO2 accumulation and efflux rates of 3 S. cerevisiae strains and 3 B.
bruxellensis strains were determined. It was shown that the S. cerevisiae strains followed the
same trends as previously found in literature whereas B. bruxellensis strains showed similar
trends but displayed highly variable strain-dependent results. B. bruxellensis CB63 and S. cerevisiae VIN13 were investigated for their response to SO2 in two
different media, TA and SWM, over a 48-hour and 32-day period respectively. Acetic acid,
acetaldehyde, D-glucose, D-fructose (only in SWM) and ethanol (only in TA) were regularly
monitored over the time course of each experiment. SO2 had the greatest impact on
B. bruxellensis with decreased rates of glucose consumption and ethanol production as well as
increased acetic acid. Acetaldehyde peaked shortly after SO2 addition with the subsequent
restarting of sugar consumption for certain samples. This suggests that sufficient acetaldehyde
was produced to bind free SO2 to reduce SO2 stress. Volatile phenols were quantified for day 32
of the SWM experiment. An increase of 4-ethyl guaiacol was correlated to higher molecular SO2
levels. SO2 negatively affected both yeasts energy metabolism, forcing the yeasts metabolism
to adapt to ensure survival.
In general, SO2 was shown to have a negative impact on all aspects of a yeasts growth and
metabolism and that SO2 tolerance is highly strain dependent and a far more complicated
characteristic than currently understood. / AFRIKAANSE OPSOMMING: Die gis Brettanomyces is in 1904 uit bier geïsoleer en daarna met wyn geassosieer. 'n
sporulerende vorm, Dekkera, is later ontdek. Brettanomyces bruxellensis produseer hoë vlakke
van vlugtige fenol afgeure in wyn. Swaweldioksied (SO2) is die mees gebruikte chemiese
preserveermiddel in wyn. Giste het verskeie meganismes om SO2 te hanteer, naamlik Ssu1p, 'n
membraan-gebonde SO2 transporter, sulfietvermindering, sulfiet-oksidasie en
asetaldehiedproduksie. In ongunstige omgewingstoestande kan sekere giste 'n lewensvatbare,
maar nie-kultiveerbare (LMNK)-toestand aanneem wat gekenmerk word deur verlaagde
metaboliese tempo, onvermoë om voort te plant op soliede media en 'n vermindering van die
selgrootte. LMNK kan veroorsaak word deur chemiese stres, soos hoë SO2-vlak. Die doelwitte
van hierdie studie was om die SO2 -bestandheid van B. bruxellensis en Saccharomyces
cerevisiae te ondersoek, hul spoed van SO2 -opneming/akkumulasie en -uitskeiding te
kwantifiseer, die invloed van SO2 op energiemetabolisme te bepaal en te ondersoek of B.
bruxellensis oor ‘n soortgelyke geen as die S. cerevisiae SSU1 beskik.
In hierdie studie is die identiteit van 'n aantal Brettanomyces/Dekkera-stamme bevestig deur
5.8S rDNA-ITS RFLP-analise en DNA-opeenvolging te gebruik. Sporulasietoetse is gebruik om
te bevestig of hierdie stamme aan die genus Dekkera of Brettanomyces behoort. 'n Metode om
SO2 onder laboratoriumtoestande akkuraat te kwantifiseer, is geoptimiseer. Molekulêre SO2-
bestandheid is getoets deur vars giskulture op media met SO2 en/of etanol te groei.
Bestandheid teen SO2 en/of etanol het stam-afhanklike resultate getoon, S. cerevisiae wat die
hoogste toleransievlakke getoon het, terwyl B. bruxellensis SO2 en etanol swak tolereer, maar
sekere stamme het goed gegroei met slegs SO2. Die SO2-akkumulasie en -uitskeidingtempo
van 3 S. cerevisiae-rasse en 3 B. bruxellensis-stamme is bepaal. Daar is gevind dat die S.
cerevisiae-rasse dieselfde tendens soos voorheen in die literatuur beskryf, gevolg het, terwyl B.
bruxellensis-stamme soortgelyke tendense getoon het,maar hoogs veranderlike stamafhanklike
resultate vertoon. B. bruxellensis CB63 en S. cerevisiae VIN13 is ondersoek vir hul reaksie tot SO2 in twee
verskillende media, TA en SWM, oor 'n tydperk van 48-uur en 32-dae onderskeidelik. Asynsuur,
asetaldehied, D-glukose, D-fruktose (slegs in SWM) en etanol (slegs in TA) is gereeld
gemoniteer oor die verloop van elke eksperiment. SO2 het die grootste impak op B. bruxellensis
met ‘n verlaagde tempo van glukoseverbruik en etanolproduksie, sowel as verhoogde asynsuur.
‘n Asetaldehiedhoogtepunt is bereik kort na die SO2-byvoeging met die daaropvolgende
hervatting van suiker wat vir sekere monsters gebruik is. Dit dui daarop dat voldoende
asetaldehied geproduseer is om vry SO2 te bind om SO2-stres te verminder. Vlugtige fenole is
op dag 32 van die SWM-eksperiment gekwantifiseer. 'n Toename van 4-etiel-guajakol korreleer
met hoër molekulêre SO2-vlakke. SO2 het beide giste se energiemetabolisme negatief
beïnvloed, wat die gis dwing om sy metabolisme aan te pas om oorlewing te verseker. Oor die algemeen het SO2 'n negatiewe impak op alle aspekte van giste se groei en
metabolisme, en SO2-bestandheid is hoogs stam–afhanklik. Dit is ook 'n baie meer
ingewikkelde kenmerk as wat tans verstaan word.
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Efeito da concentração de SO2 nas reações de calcinação e sulfatação de calcários em reator de leito fluidizado / Effect of the concentration of S02 in the reactions of calcination and sulfatation in a fluidized bed reactorJulio Edgardo Lindo Samaniego 21 November 2003 (has links)
Foi realizado um estudo sobre o efeito das concentrações de SO2 na sua absorção por calcários em fornalhas de leito fluidizado. Para observar a influência do SO2 sobre os diferentes parâmetros físicos e químicos do processo, foram criadas atmosferas compostas por quatro concentrações diferentes de SO2, que foram de 500, 1.000, 2.000 e 4.000 ppm. Utilizou-se ainda dois tipos de calcários, o Dolomítico-DP e o Calcítico-CI. O leito fluidizado borbulhante utilizado, possuía 160 mm de diâmetro interno e foi fluidizado com ar à temperatura de 850ºC, contendo SO2 na concentração desejada. Como material do leito foi utilizada areia de quartzo (99,9%), com diâmetro de 385 μm e aproximadamente 3,0 Kg de massa. O calcário foi adicionado em bateladas de 50 g com o reator já pré-aquecido, enquanto as variações das concentrações dos gases SO2, CO2, CO e O2 e suas descargas foram monitoradas continuamente na saída do ciclone que era utilizado para retenção do particulado fino. Para adquirir esses dados foi desenvolvido um programa em LabView. O modelo matemático escolhido possibilitou a determinação da conversão, da taxa de conversão e do coeficiente global de taxa de reação para todas as condições testadas. / A study of the effect of the concentrations of SO2 in its absorption by limestones in fluidized bed furnaces was conducted. For the determination of the SO2 influence on the different physical and chemical parameters of process, such as calcinations and sulfatation four different atmospheres were used in the reator with concentrations of SO2 of 500, 1.000, 2.000 and 4.000 ppm. Two types of limestones were used : Dolomitico-DP and Calcitico-CI. The bench scale bubbling fluidized bed reactor had a 160 mm internal diameter and was fluidized with air at 850ºC containing the required concentration of SO2. Bed material was quartz sand (99,9%), with 385 μm diameter and approximately 3 Kg of mass. The limestone was introduced in samples of 50 g, in the reactor previously stabilized, and the concentration of the gases SO2, CO2, CO and O2 and their discharges in the reactor exit were continually monitored. For the recording of this parameters a data acquisition program in LabView was developed. A mathematical model was used to allow the determination of the conversion, the conversion rate and the global coefficient of reaction rate for all the tested conditions.
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Snížení emisí SO2 ve spalinách z fluidního kotle / Reducing emissions of SO2 in the flue gas from the fluidized bed boilerTesař, Jan January 2016 (has links)
Aim of this thesis is to design a technology of a flue gas desulphurization of fluidized bed boiler. Currently, the state of technology is not able to provide flue gas desulphurisation to required level. For this reason it is necessary to build additional device for the desulphurisation. Theoretical part of the thesis deals with the emission limits of sulphur dioxide, available methods of desulphurization and sorbents suitable for the desulfurization. In practical part conditioned dry sorption method is chosen for the specified source, technological and structural design for suggested desulphurization technology including design of all device is proposed. The thesis also includes a technology design and a 3D model.
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Pt and Au as electrocatalysts for various electrochemical reactions / Marthinus Hendrik SteynSteyn, Marthinus Hendrik January 2015 (has links)
In this study the focus was on the electrochemical techniques and aspects behind the
establishment of the better catalyst (platinum or gold) for the sulphur dioxide oxidation
reaction (SDOR). One of the primary issues regarding the SDOR is the catalyst material,
thus the comparative investigation of the performance of platinum and gold in the SDOR, as
found in this study. Ultimately, the SDOR could lead to an effective way of producing
hydrogen gas, which is an excellent energy carrier.
The electrochemical application of the oxygen reduction reaction (ORR) and ethanol
oxidation reaction (EOR) is an integral part of the catalytic process of water electrolysis, and
by using fuel cell technology, it becomes even more relevant to this study and can therefore
be used as a control, guide and introduction to the techniques required for electrochemical
investigation of catalyst effectiveness. Subsequently, the EOR as well as the ORR was used
as introduction into the different electrochemical quantification and qualification techniques
used in the electrochemical analyses of the SDOR.
Considering the ORR, gold showed no viable activity in acidic medium, contrarily in alkaline
medium, it showed good competition to platinum. Gold also lacked activity towards the EOR
in acidic medium compared to platinum, with platinum the best catalyst in both acidic and
alkaline media. Ultimately, platinum was established to be the material with better activity for
the ORR with gold a good competitor in alkaline medium, and platinum the better catalyst for
the EOR in both acidic and alkaline media.
With the main focus of this study being the SDOR, gold proved to be the best catalyst in salt
and gaseous forms of SO2 administration compared to platinum when the onset potential,
maximum current density, Tafel slope and number of electrons transferred are taken into
consideration. The onset potential was determined as 0.52 V vs. NHE for both platinum and
gold using SO2 gas and 0.54 V and 0.5 V for gold and platinum respectively, using Na2SO3
salt. The maximum current density using gaseous SO2 for platinum at 0 RPM was 400
mA/cm2 with a Tafel slope of 891 mV/decade whereas gold had a maximum current density
of 300 mA/cm2 and a Tafel slope of 378 mV/decade. Using Na2SO3 salt, the maximum
current density of gold was 25 mA/cm2 with a Tafel slope of 59 mV/decade whereas
platinum only achieved 18 mA/cm2 with a Tafel slope of 172 mV/decade. Concerning the
number of electrons transferred, gold achieves a transfer of 2 while platinum only 1 for both
SO2 gas and Na2SO3 salt. Taking all these summarised determinations into account, gold
was established to be a very competitive catalyst material for the SDOR, compared to
platinum. / MSc (Chemistry), North-West University, Potchefstroom Campus, 2015
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