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Evaluation and Quantification of Engineered Flocs and Drinking Water TreatabilityArnold, Adam January 2008 (has links)
Jar tests are performed to simulate full-scale pre-treatment and particle removal processes. Operators typically conduct them in an effort to attempt alternative treatment doses and strategies without altering the performance of the full-scale drinking water treatment plant. However, information obtained from these tests must be evaluated judiciously, as they currently focus on reduction of specific water quality parameters (i.e., ultraviolet absorption at 254 nm (UV254) and turbidity), and measuring and understanding the significance of coagulant dose on floc size. Consideration of aggregate structure has been less explored due mainly to a lack of appropriate theories to describe the complex random floc structure. Improving the predictive capacity of bench-scale protocols commonly used for optimizing conventional chemical pre-treatment in full-scale drinking water treatment plants is required.
Results from settling tests indicated that the production of larger and more settleable flocs could not be described by floc settling velocities and floc sizes. Settling velocities were not directly related to either UV254 or turbidity reductions. Results of the floc characterization tests indicated that measured values of UV254 and turbidity of the supernatant were generally inversely proportional to aggregate D90; that is, the residual UV254 and/or turbidity decreased as the value of D90 increased, which may have been indicative of flocculent settling. No direct relationship could be discerned between fractal dimension D1 (i.e., floc shape) and the UV254 and turbidity of the supernatant; however, the turbidity after flocculation and a period of settling appeared to be inversely proportional to fractal dimension D2 (i.e., porosity). Overall, the results of the experiments have demonstrated that grain size distributions and fractal dimensions might be used to assess and/or predict pre-treatment and/or particle removal performance. Specifically, the relationship between D90 values calculated from samples of flocculated water prior to settling and UV254 and turbidity values of that water after a period of settling may be a simple tool that can be utilized to describe and potentially better predict flocculent settling performance. At present, this appears to be the first such tool of its kind that has been reported.
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Evaluation and Quantification of Engineered Flocs and Drinking Water TreatabilityArnold, Adam January 2008 (has links)
Jar tests are performed to simulate full-scale pre-treatment and particle removal processes. Operators typically conduct them in an effort to attempt alternative treatment doses and strategies without altering the performance of the full-scale drinking water treatment plant. However, information obtained from these tests must be evaluated judiciously, as they currently focus on reduction of specific water quality parameters (i.e., ultraviolet absorption at 254 nm (UV254) and turbidity), and measuring and understanding the significance of coagulant dose on floc size. Consideration of aggregate structure has been less explored due mainly to a lack of appropriate theories to describe the complex random floc structure. Improving the predictive capacity of bench-scale protocols commonly used for optimizing conventional chemical pre-treatment in full-scale drinking water treatment plants is required.
Results from settling tests indicated that the production of larger and more settleable flocs could not be described by floc settling velocities and floc sizes. Settling velocities were not directly related to either UV254 or turbidity reductions. Results of the floc characterization tests indicated that measured values of UV254 and turbidity of the supernatant were generally inversely proportional to aggregate D90; that is, the residual UV254 and/or turbidity decreased as the value of D90 increased, which may have been indicative of flocculent settling. No direct relationship could be discerned between fractal dimension D1 (i.e., floc shape) and the UV254 and turbidity of the supernatant; however, the turbidity after flocculation and a period of settling appeared to be inversely proportional to fractal dimension D2 (i.e., porosity). Overall, the results of the experiments have demonstrated that grain size distributions and fractal dimensions might be used to assess and/or predict pre-treatment and/or particle removal performance. Specifically, the relationship between D90 values calculated from samples of flocculated water prior to settling and UV254 and turbidity values of that water after a period of settling may be a simple tool that can be utilized to describe and potentially better predict flocculent settling performance. At present, this appears to be the first such tool of its kind that has been reported.
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Lignite Derived Humic Substances for Treatment of Acid Mine DrainageOlds, William January 2011 (has links)
Addition of alkalinity to acid mine drainage (AMD) results in the neutralisation of acidity and precipitation of dissolved metals as insoluble hydroxides. Two aspects of the current AMD treatment practice at the Stockton Mine could be enhanced. Firstly, residual water quality may be poor due to unreacted alkalinity reagents, particularly CaCO3, resulting in poor water clarity and elevated suspended solids (SS). Secondly, neutralisation to circum-neutral pH may not avoid the discharge of residual metals (Ni and Zn) due to incomplete adsorption and hydroxide precipitation.
The aim of this project was to enhance the conventional neutralisation of AMD through addition of humic substances (HS) to reduce residual SS and trace metal concentrations. Humic substances are organically derived and have a high molecular weight. Functional groups on the surface of HS are capable of binding dissolved metals, forming HS-metal complexes. Incorporation of HS complexed metals into settling floc could result in increased metal removal from the dissolved phase.
Modified jar testing was used to investigate the effects of HS addition before, after and during (pH 4.5) neutralisation of AMD in two treatment scenarios at the Stockton Mine; the Blackwater Treatment Plant (BTP) using NaOH and Ca(OH)2 and the Mangatini Stream-sump System (MSS) using CaCO3. Supernatant samples collected during the sedimentation period were analysed for basic water quality parameters (turbidity and suspended solids) and dissolved (< 0.45 µm) metal concentrations.
The addition of HS to the BTP process before (pH 2.8) and during (pH 4.5) neutralisation resulted in HS precipitation. Precipitated HS subsequently acted as a nucleation site, triggering flocculation of precipitating metal hydroxides, resulting in low turbidity and suspended solids (SS) of less than 2 NTU and 5 mg/L, respectively. The addition of HS after neutralisation (pH 7) did not result in HS precipitation. Intermolecular bridging of HS by the divalent Ca resulted in incorporation of HS into floc when neutralised by Ca(OH)2, resulting in low turbidity and SS. However, in NaOH neutralised conditions, the monovalent Na was unable to bridge HS molecules, resulting in HS remaining dissolved and contributing to elevated turbidity and SS of up to 24.4 NTU and 18.4, respectively.
The neutralisation efficiency of CaCO3 is relatively low, thus approximately 1000 mg/L CaCO3 remained unreacted in MSS scenarios, resulting in elevated turbidity and SS. When added after neutralisation, dissolved Solid Energy Humic Acid (SEHA) facilitated flocculation of residual CaCO3 SS, resulting in an up to 75% lower suspended solids than CaCO3 neutralisation alone conditions. Although the results are good, the efficiency of SEHA as a polymer compared unfavorably in a cost: benefit analysis to two commercially available polymers for the removal of residual CaCO3.
Neutralisation of AMD in control samples resulted in decreased concentrations of the target metal group (Ni, Zn, Cu, Cd, and Pb) by hydroxide precipitation, co-precipitation, and adsorption. Equilibrium speciation modeling showed that the HS-metal binding affinity controlled the effectiveness of HS addition for metal removal. The low HS complexation affinity of Ni and Zn resulted in no additional metal removal by HS dosing. The removal of Cu was enhanced by over 50% for SEHA 20 during-neutralisation conditions neutralised by both NaOH and Ca(OH)2. Up to 80% lower Cd concentrations were observed for all HS dose conditions when neutralised by Ca(OH)2. Data for CaCO3 HS dosed metal removal was statistically indeterminate. The high detection limit for Pb made any HS dosed removal enhancement difficult to identify, which was unfortunate as Pb has a high HS complexation affinity (Čežı́ková, Kozler et al. 2001; Milne, Kinniburgh et al. 2003). A simple cost: benefit analysis showed that the additional removal of metals by HS dosing was less efficient than conventional neutralisation alone, on a cost basis.
Overall, incorporation of HS into AMD treatment results in improved water quality for CaCO3 neutralisation and lower concentrations of metals with a high HS binding affinity, for some conditions. However, further investigation is required to improve the feasibility of HS incorporation into the AMD neutralisation process.
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The potential for Charophyte re-establishment in large, shallow, eutrophic lakes with special reference to Lake Waikare, New Zealand.Hopkins, Aareka January 2006 (has links)
Lake Waikare is a large, shallow eutrophic lake devoid of submerged macrophytes. I investigated potential methods for re-establishing submerged macrophytes in the lake. Specifically, I subjected charophyte (Chara corallina) plantlets to two treatments of exposure in the lake (in areas exposed and sheltered from wind) to test for survival and growth under these conditions, and inside and outside fish exclosures to test for growth and survival in the presence of fish. While plantlets grew outside the exclosures in winter, their accumulated biomass over 21 days was less than protected plantlets. In winter, the accumulated biomass was lower outside than inside exclosures (by ~40%) at the sheltered site and was lower outside than inside exclosures (by 43%) at the exposed site. Overall, growth rates in winter were higher at the sheltered site (compared to the exposed site) by ~7%. In summer, charophyte accumulated biomass inside the exclosures increased by 85%, while at the sheltered site accumulated biomass increased by 58%. Outside the exclosures in summer the plantlets were completely removed at both sites. Overall, growth rates where higher at the exposed site than the sheltered site by 31%. Fish were responsible for the partial removal of plantlets in winter and total removal of plantlets in summer, and therefore affect the survival and growth of charophytes in Lake Waikare. The embayment at the sheltered site provides the best location in winter for re-establishment of charophytes from oospores because better growth rates were obtained there, and its sheltered location provides protection from severe wave action found at the exposed site. Oospores did not germinate after being submersed in the lake for 90 days due to heavy sedimentation. To induce an improvement in the present light climate, Alum was tested to determine its effectiveness and longevity for settling lake sediments to allow charophytes to establish and grow. Examining the settling rates of Lake Waikare sediments and water treated with Alum over a range of suspended sediment concentrations and time intervals, sediments settled faster with Alum than without for at least 15 days (at 200 g l^1 suspended sediment concentration) and it remained active to 60 days but at reduced effectiveness. At the other concentrations tested (100 g l^1 and 300 g l^1 suspended sediment concentration), Alum responses were insignificant. An improved light climate achieved by fish removal or Alum treatment will likely not be sufficient to permit the re-establishment of submerged macrophytes due to the turbid, algal-dominated state of the lake. The present nutrient and sediment levels, wave climate and fish influence must be mitigated so charophyte plantlets can be established.
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The effect of pre-ozonation on the physical characteristics of raw water and natural organic matter (NOM) in raw water from different South African water resources / Ayesha Hamid CarrimCarrim, Ayesha Hamid January 2006 (has links)
Research in the use of ozone in water treatment conducted by many authors support the idea that
the nature and characteristics of natural organic matter (NOM) present in raw water determines the
efficiency of ozonation in water purification.
An ozone contact chamber was designed and made to allow pre-ozonation of water to take place.
The concentration of ozone in the chamber was determined using the Indigo method. For the
duration of one year, water samples were collected from four different sampling sites and analyzed
to determine their overall ecological status with regard to several variables such as pH, chlorophyll-a,
SAC254, turbidity, DOC, algal species composition and sum of NOM. Two dams sites and two
riverine sites were chosen, Hartbeespoort Dam (a hyper-eutrophic impoundment), Boskop Dam (a
mesotrophic impoundment), Midvaal Water Company at Orkney and Sedibeng Water at Bothaville.
The samples were treated in Jar Tests with FeCI3 and the same variables were measured. Preozonation
followed by Jar Tests was performed on each sample at twoconcentrations of ozone and
the variables were measured to examine the efficiency of ozonation.
In general, the ph was high and stayed the same for all the samples and for all the treatments.
DOC was variable and showed no relationship to any other variable or to the treatments.
Hartbeespoort Dam was found to be a eutrophic impoundment characterized by high algal bloom of
the cyanobacteria Microcystis sp., Turbidity, SAC254, and the sum of NOM were lower than for the
riverine sites but higher than for Boskop Dam. The NOM constituted more intermediate molecular
weight(1MW)and low molecular weight (LMW) fractions than the riverine sites. Ozone was effective
in reducing chlorophyll-a, turbidity and SAC254 from Hartbeespoort Dam, but the presence of large
numbers of algal cells interferes with its efficiency. Release of cell-bound organics after ozonation
can lead to increases instead of decreases in these variables. Jar Test results demonstrate that
ozonation improves water quality when compared to conventional treatment although the
interference of algal cells can alter results.
Boskop Dam is a mesotrophic impoundment characterised by low productivity, low SAC254, tow
turbidity and low sum of NOM. However, it has a large portion of the LMW fraction of NOM present.
This LMW fraction affects the treatment process as this fraction is not acted upon by ozone.
Therefore it was found that ozonation did not improve the quality of the water when compared to
conventional treatment.
The two riverine sites, Midvaal and Sedibeng were similar to each other. Both sites had high algal
productivity with high chlorophyll-a values indicative of algal blooms observed at certain times.
These blooms consisted either of members of Bacillariophyceae or Chlorophyceae. High turbidity
and SAC254 was observed during the rainy season and was related to the high percentage HMW
and IMW fractions of NOM present. There was correlation between the turbidity and SAC254 of
these sites leading to the assumption that the turbidity of the river is due to the presence of HMW
humic fractions of NOM. Ozonation was effective in improving water quality with respect to turbidity,
SAC254 and chlorophyll-a removal, both on its own and after conventional treatment when
combined with a coagulant. However, the species of algae present affects ozonation as members
of Bacillariophyceae are not affected by the actions of ozone because of the presence of a silica
frustule whereas members of Chlorophyceae are easily removed by ozone.
In general, ozone acts upon the HMW and LMW fractions of NOM causing them to breakdown into
smaller fractions. Ozone has no effect on samples that have a high percentage of the LMW fraction
of NOM. This LMW fraction is more readily removed by conventional treatment than by ozonation.
The presence of large numbers of algal cells as well as the species of cells can negatively affect
the treatment process with regard to ozone. / Thesis (M. Environmental Science (Water Science))--North-West University, Potchefstroom Campus, 2007.
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The effect of pre-ozonation on the physical characteristics of raw water and natural organic matter (NOM) in raw water from different South African water resources / Ayesha Hamid CarrimCarrim, Ayesha Hamid January 2006 (has links)
Research in the use of ozone in water treatment conducted by many authors support the idea that
the nature and characteristics of natural organic matter (NOM) present in raw water determines the
efficiency of ozonation in water purification.
An ozone contact chamber was designed and made to allow pre-ozonation of water to take place.
The concentration of ozone in the chamber was determined using the Indigo method. For the
duration of one year, water samples were collected from four different sampling sites and analyzed
to determine their overall ecological status with regard to several variables such as pH, chlorophyll-a,
SAC254, turbidity, DOC, algal species composition and sum of NOM. Two dams sites and two
riverine sites were chosen, Hartbeespoort Dam (a hyper-eutrophic impoundment), Boskop Dam (a
mesotrophic impoundment), Midvaal Water Company at Orkney and Sedibeng Water at Bothaville.
The samples were treated in Jar Tests with FeCI3 and the same variables were measured. Preozonation
followed by Jar Tests was performed on each sample at twoconcentrations of ozone and
the variables were measured to examine the efficiency of ozonation.
In general, the ph was high and stayed the same for all the samples and for all the treatments.
DOC was variable and showed no relationship to any other variable or to the treatments.
Hartbeespoort Dam was found to be a eutrophic impoundment characterized by high algal bloom of
the cyanobacteria Microcystis sp., Turbidity, SAC254, and the sum of NOM were lower than for the
riverine sites but higher than for Boskop Dam. The NOM constituted more intermediate molecular
weight(1MW)and low molecular weight (LMW) fractions than the riverine sites. Ozone was effective
in reducing chlorophyll-a, turbidity and SAC254 from Hartbeespoort Dam, but the presence of large
numbers of algal cells interferes with its efficiency. Release of cell-bound organics after ozonation
can lead to increases instead of decreases in these variables. Jar Test results demonstrate that
ozonation improves water quality when compared to conventional treatment although the
interference of algal cells can alter results.
Boskop Dam is a mesotrophic impoundment characterised by low productivity, low SAC254, tow
turbidity and low sum of NOM. However, it has a large portion of the LMW fraction of NOM present.
This LMW fraction affects the treatment process as this fraction is not acted upon by ozone.
Therefore it was found that ozonation did not improve the quality of the water when compared to
conventional treatment.
The two riverine sites, Midvaal and Sedibeng were similar to each other. Both sites had high algal
productivity with high chlorophyll-a values indicative of algal blooms observed at certain times.
These blooms consisted either of members of Bacillariophyceae or Chlorophyceae. High turbidity
and SAC254 was observed during the rainy season and was related to the high percentage HMW
and IMW fractions of NOM present. There was correlation between the turbidity and SAC254 of
these sites leading to the assumption that the turbidity of the river is due to the presence of HMW
humic fractions of NOM. Ozonation was effective in improving water quality with respect to turbidity,
SAC254 and chlorophyll-a removal, both on its own and after conventional treatment when
combined with a coagulant. However, the species of algae present affects ozonation as members
of Bacillariophyceae are not affected by the actions of ozone because of the presence of a silica
frustule whereas members of Chlorophyceae are easily removed by ozone.
In general, ozone acts upon the HMW and LMW fractions of NOM causing them to breakdown into
smaller fractions. Ozone has no effect on samples that have a high percentage of the LMW fraction
of NOM. This LMW fraction is more readily removed by conventional treatment than by ozonation.
The presence of large numbers of algal cells as well as the species of cells can negatively affect
the treatment process with regard to ozone. / Thesis (M. Environmental Science (Water Science))--North-West University, Potchefstroom Campus, 2007.
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Separate treatment of wash water from sand filter using disc filter technology.González Sánchez, María Fernanda January 2013 (has links)
The purpose of this study is to evaluate the convenience and effectiveness of using a disc filter to treat washing water from the sand filters at Sundet wastewater treatment plant. The disc filter is used aiming for the reduction of suspended solids and phosphorus. The study was divided in two main experimental stages. During the first stage laboratory jar-tests were performed in order to identify which flocculation aid was more suitable, this was further on used to improve the water treatment. Based on the laboratory trials results, two different polymers (1 and 2) were chosen to be tested at pilot scale. The second stage involved the pilot filter operation itself; this period was as well divided in two sub-stages where filter cloths with two different pore openings were tested. During the first sub-stage the pilot operated with an 18 μm pore opening filters cloth and both polymers. At the end of the first half polymer 1 showed to be more efficient and so it was further used throughout the second sub-stage in combination with a 10μm pore opening filter cloth. As from theoretical knowledge the phosphorus and suspended solid removal were expected to be between 75% and 90%, results which were achieved during both laboratory trials and pilot filter. The best results were observed with the 10μm pore opening filter cloth and polymer 1. Also, additional results from pilot trials performed at Sundet after the study period are presented.
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Kalciumklorid som hjälpkoagulant / Calcium Chloride as a Co-CoagulantHägg, Kristofer January 2015 (has links)
As populations continue to grow, the demand for fresh drinking water is increasing. This puts a lot of pressure on drinking water producers to strive for more efficient solutions and techniques. Many producers worldwide use surface water as a raw water source, which they often treat through coagulation and flocculation techniques. This is done by adding coagulant (e.g. metal coagulants), creating instability in the suspension, causing flocculation. In this work, PIX-311 (a FeCl3 coagulant produced by Kemira) and Al2(SO4)3 (Kemwater ALG) were used as primary coagulants and CaCl2 (produced by TETRA Chemicals) as an adjunct in a coagulation and flocculation study. The goal of this work was to study the effects of CaCl2 additions to Fe(III) and Al(III) flocculation. The experiments were conducted at Ringsjöverket (a water treatment facility), using jar tests to simulate the treatment process on a laboratory scale. The raw water samples used in this study, were taken from Bolmen, a lake in southern Sweden. A spectrophotometer was used to monitor the efficiency of flocculation by UV-VIS absorption. In the first experiments, various CaCl2 additions were added to Fe(III) flocculation, with FeCl3 as a primary coagulant. To see if FeCl3 could be substituted with CaCl2, the amount of primary coagulant was reduced to about 80% of the optimal dosage (the dose used daily by the water treatment plant). In the next series of experiments, various amounts of CaCl2 were added with an optimal dose of FeCl3. After that, the effects of CaCl2 additions to Al(III) flocculation were conducted, using Al2(SO4)3 as a primary coagulant. The experiments followed the previous scheme used in Fe(III) flocculation. The UV-VIS results showed that no CaCl2 additions were effective enough to replace the primary coagulant. However, reduced amount of primary coagulant benefited slightly from small CaCl2 additions. A likely explanation for this is the ability of Ca2+ to aid in charge neutralization and reduce the repulsive forces between particles in suspension, aiding coagulation. Furthermore, CaCl2 additions, with reasonable certainty, did not increase the efficiency of Fe(III) flocculation. When the CaCl2 dose was increased (from about 13µl to 820 µl per liter raw water), the effect became negative. In other words, high doses of CaCl2 inhibited flocculation by, most likely, occupying adsorption sites for the primary coagulant. This was observed for an optimal FeCl3 dose, reduced FeCl3 dose and an optimal dose of Al2(SO4)3. In the more brief study on Al(III) flocculation, low CaCl2 doses did not appear to have any effect on flocculation at first. However, when a reduced amount of Al2(SO4)3 was used, the samples with CaCl2 gave better UV-VIS results once the pH was increased from 6 to about 6.15. One explanation for this could be that the shift in flocculation mechanism at higher pH, causes CaCl2 to have an increased positive effect.
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Ensaios de tratabilidade aplicados a determina??o de par?metros para dimensionamento de processos de tratamento de ?gua de manancial eutrofizadoEust?quio, Hugo Mozer Barros 17 December 2010 (has links)
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Previous issue date: 2010-12-17 / Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior / Eutrophication is a growing process present in the water sources located in the
northeast of Brazil. Among the main consequences of these changes in trophic levels
of a water source, stands out adding complexity to the treatment to achieve water
standards. By these considerations, this study aimed to define, on a laboratory scale,
products and operational conditions to be applied in the processing steps using raw
water from Gargalheiras dam, RN, Brazil. The dam mentioned shows a high number
of cyanobacteria, with a concentration of cells / ml higher than that established by
Decree No. 518/04 MS. The same source was also considered by the state
environmental agency in 2009 as hypereutrophic. The static tests developed in this
research simulated direct filtration (laboratory filters) and pre-oxidation with chlorine
and powdered activated carbon adsorption. The research included the evaluation of
the coagulants aluminum hydrochloride (HCA) and alum (SA). The development of
the research investigated the conditions for rapid mixing, the dosages of coagulants
and pHs of coagulation by the drawing of diagrams. The interference of filtration rate
and particle size of filtering means were evaluated as samples and the time of
contact were tested with chlorine and activated carbon. By the results of the
characterization of the raw water source it was possible to identify the presence of a
high pH (7.34). The true color was significant (29 uH) in relation to the apparent color
and turbidity (66 uH and 13.60 NTU), reflecting in the measurement of organic
matter: MON (8.41 mg.L-1) and Abs254 (0.065 cm-1). The optimization of quick mix
set time of 17", the speed gradient of 700 s-1 in the coagulation with HCA and the
time of 20" with speed gradient of 800 s-1 for SA. The smaller particle sizes of sand
filtering means helped the treatment and the variation in filtration rate did not affect
significantly the efficiency of the process. The evaluation of the processing steps
found adjustment in standard color and turbidity of the Decree n? 518/04 MS, taking
in consideration the average values found in raw water. In the treatment using the
HCA for direct filtration the palatable pattern based on the apparent color can be
achieved with a dose of 25 mg L-1. With the addition of pre-oxidation step, the
standard result was achieved with a reduced dose for 12 mgHCA.L-1. The turbidity
standard for water was obtained by direct filtration when the dose exceeds 25 mg L-1
of HCA. With pre-oxidation step there is the possibility of reducing the dose to 20 mg
L-1.The addition of CAP adsorption, promoted drinking water for both parameters,
with even lower dosage, 13 mg L-1 of HCA. With coagulation using SA removal
required for the parameter of apparent color it was achieved with pre-oxidation and
22 mgSA.L-1. Despite the satisfactory results of treatment with the alum, it was not
possible to provide water with turbidity less than 1.00 NTU even with the use of all
stages of treatment / A eutrofiza??o ? um processo cada vez mais presente nos mananciais
situados no nordeste brasileiro. Entre as principais conseq??ncias destas altera??es
nos n?veis tr?ficos da ?gua de um manancial destaca-se o acr?scimo de
complexidade ao tratamento para potabiliza??o. Mediante a estas considera??es,
este trabalho teve como objetivo definir, em escala de laborat?rio, produtos e
condi??es operacionais a serem empregadas em etapas de tratamento utilizando
?gua bruta do a?ude Gargalheira, RN, Brasil. O a?ude em quest?o demonstra um
n?mero de cianobact?rias elevado, apresentando uma concentra??o de c?lulas/ml
superior aos n?veis estabelecidos pela Portaria MS n? 518/04. O mesmo, ainda foi
considerado pelo ?rg?o ambiental do estado no ano de 2009 como hipereutr?fico.
Os ensaios est?ticos desenvolvidos neste trabalho simularam filtra??o direta (filtros
de laborat?rio), pr?oxida??o com cloro e adsor??o por carv?o ativado pulverizado.
Foram avaliados os coagulantes hidr?xicloreto de alum?nio (HCA) e sulfato de
alum?nio granulado (SA). O desenvolvimento da pesquisa buscou otimiza??o das
condi??es de mistura r?pida, das dosagens de coagulantes e pHs de coagula??o
com a constru??o de diagramas. As interfer?ncias da taxa de filtra??o e a
granulometria do meio filtrante foram avaliadas e testaram-se dosagens e tempos de
contato com cloro e com o carv?o ativado. Com os resultados da caracteriza??o da
?gua bruta foi poss?vel identificar no manancial a presen?a de um pH elevado (7,34).
A cor verdadeira foi significativa (29 uH) em rela??o ? cor aparente e turbidez (66 uH
e 13,60 uNT), refletindo-se nas medidas de mat?ria org?nica: MON (8,41 mg.L-1) e
Abs254 (0,065 cm-1). A otimiza??o da mistura r?pida definiu o tempo de 17 ,
gradiente de velocidade de 700 s-1 na coagula??o com HCA e tempo de 20 ,
gradiente de velocidade de 800 s-1 para o SA. Granulometrias menores da areia do
meio filtrante favoreceram o tratamento e a varia??o na taxa de filtra??o n?o
interferiu de forma significativa na efici?ncia do processo. A avalia??o das etapas de
tratamento verificou a adequa??o aos padr?es de cor aparente e turbidez da Portaria
MS 518/2004 tomando como base os valores m?dios encontrados na ?gua bruta. No
tratamento utilizando o HCA por filtra??o direta, a potabilidade para a cor aparente
pode ser atingida com uma dosagem de 25 mg.L-1. Adicionando a etapa de
pr?oxida??o o padr?o foi atingido com dosagem reduzida para 12 mgHCA.L-1. Para
a turbidez a potabilidade foi obtida na filtra??o direta quando a dosagem supera 25
mg.L-1 de HCA. Com etapa de pr?oxida??o h? a possibilidade de redu??o da
dosagem para 20 mg.L-1 de coagulante. O acr?scimo da adsor??o em CAP,
promoveu a potabilidade para os dois par?metros, com dosagem ainda menor, 13
mg.L-1 de HCA. Coagulando com SA a remo??o necess?ria para o par?metro de cor
aparente foi atingida com pr?oxida??o e dosagem de 22 mgSA.L-1. Apesar de
apresentar bons resultados o tratamento com o sulfato de alum?nio n?o foi capaz de
fornecer ?gua com turbidez menor que 1,00 uNT mesmo com a utiliza??o de todas
as etapas de tratamento
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Modelový výzkum účinnosti separačních technologií úpravy vody / Model research on the effectiveness of separation technologies for water treatmentHofmanová, Lucie January 2019 (has links)
This diploma thesis deals with the effectiveness of separation technologies for water treatment. The first theoretical part mentions types of pollution that can be found in surface water. Furthermore, the interparticle interactions affecting the stability of colloidal dispersions are discussed. The following is a description of the principle, procedure, mechanisms of coagulation and factors influencing this process. The chapter dealing with types of water treatment is followed by a more detailed description of the individual separation technologies used in the water treatment plants. The important passage in the theoretical part is the description of materials and reagents used in laboratory experiments. The coagulants nanoiron and sodium water glass are characterized, as well as Bayoxide E33, CFH 0818, FILTRASORB 100 activated charcoal and DORSILIT silicate sand. The experimental part of the thesis analyses the jar test procedure. The flocculation tester intended for the jar test was used for laboratory coagulation using nanoiron and sodium water glass. The effectiveness of selected coagulants in the removal of turbidity from water during sedimentation of flakes produced in reaction vessels was investigated. In addition, the effectiveness of individual filtering materials in the removal of turbidity from water containing nanoiron/sodium water glass was investigated. In the end, the results of laboratory tests are compared and evaluated, including photos taken during experiments.
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