Structure of a-Si:H/a-Si1-xCx:H multilayers deposited in a reactor with automated substrate holder

This paper deals with the structural properties of a-Si:H/a-Si1-xCx: H multilayers deposited by glow-discharge decomposition of SiH4 and SiH4 and CH4 mixtures. The main feature of the rf plasma reactor is an automated substrate holder. The plasma stabilization time and its influence on the multilayer obtained is discussed. A series of a-Si:H/a-Si1-xCx: H multilayers has been deposited and characterized by secondary ion mass spectrometry (SIMS), X-ray diffraction (XRD) and transmission electron microscopy (TEM). No asymmetry between the two types of interface has been observed. The results show that the multilayers present a very good periodicity and low roughness. The difficulty of determining the abruptness of the multilayer at the nanometer scale is discussed.

Fischer-Tropsch Slurry Bubble Column Reactor Modeling

The literature part of the work reviews overall Fischer-Tropsch process, Fischer-Tropsch reactors and catalysts. Fundamentals of Fischer-Tropsch modeling are also presented. The emphasis is on the reactor unit. Comparison of the reactors and the catalysts is carried out to choose the suitable reactor setup for the modeling work. The effects of the operation conditions are also investigated. Slurry bubble column reactor model operating with cobalt catalyst is developed by taking into account the mass transfer of the reacting components (CO and H2) and the consumption of the reactants in the liquid phase. The effect of hydrostatic pressure and the change in total mole flow rate in gas phase are taken into account in calculation of the solubilities. The hydrodynamics, reaction kinetics and product composition are determined according to literature. The cooling system and furthermore the required heat transfer area and number of cooling tubes are also determined. The model is implemented in Matlab software. Commercial scale reactor setup is modeled and the behavior of the model is investigated. The possible inaccuraries are evaluated and the suggestions for the future work are presented. The model is also integrated to Aspen Plus process simulation software, which enables the usage of the model in more extensive Fischer-Tropsch process simulations. Commercial scale reactor of diameter of 7 m and height of 30 m was modeled. The capacity of the reactor was calculated to be about 9 800 barrels/day with CO conversion of 75 %. The behavior of the model was realistic and results were in the right range. The highest uncertainty to model was estimated to be caused by the determination of the kinetic rate.

Coolant Flow and Heat Transfer in Pebble-Bed Reactor Core

This thesis gathers knowledge about ongoing high-temperature reactor projects around the world. Methods for calculating coolant flow and heat transfer inside a pebble-bed reactor core are also developed. The thesis begins with the introduction of high-temperature reactors including the current state of the technology. Process heat applications that could use the heat from a high-temperature reactor are also introduced. A suitable reactor design with data available in literature is selected for the calculation part of the thesis. Commercial computational fluid dynamics software Fluent is used for the calculations. The pebble-bed is approximated as a packed-bed, which causes sink terms to the momentum equations of the gas flowing through it. A position dependent value is used for the packing fraction. Two different models are used to calculate heat transfer. First a local thermal equilibrium is assumed between the gas and solid phases and a single energy equation is used. In the second approach, separate energy equations are used for the phases. Information about steady state flow behavior, pressure loss, and temperature distribution in the core is obtained as results of the calculations. The effect of inlet mass flow rate to pressure loss is also investigated. Data found in literature and the results correspond each other quite well, considered the amount of simplifications in the calculations. The models developed in this thesis can be used to solve coolant flow and heat transfer in a pebble-bed reactor, although additional development and model validation is needed for better accuracy and reliability.

Instal•lació d'un reactor químic en una indústria farmacèutica

L’objecte del projecte és l’ampliació de la línia de producció d’una indústria farmacèutica dimensionant la fontaneria i instal•lant el reactor químic. Els antecedents són els seguents: en el Desembre de 2013,una indústria farmacèutica decideix ampliar la producciód’una línia existent de treball, instal•lant un reactor químic en paral•lel a la línia deproducció existent. Al Gener de 2014 es decideix adaptar una zona que s’utilitza com a magatzem per fer la nova producció. Per tant s’ha d’adaptar la zona com a Sala Blanca per complir amb la seva nova funcionalitat. A Febrer de 2014 es contracta un enginyer per redactar el projecte de l’adaptació de la Sala Blanca, així com les instal•lacions necessàries per posar en funcionament el Reactor químic adquirit pel client

Program hosting in communications environment with Reactor and thread pool approach

In this thesis concurrent communication event handling is implemented using thread pool approach. Concurrent events are handled with a Reactor design pattern and multithreading is implemented using a Leader/Followers design pattern. Main focus is to evaluate behaviour of implemented model by different numbers of concurrent connections and amount of used threads. Furthermore, model feasibility in a PeerHood middleware is evaluated. Implemented model is evaluated with created test environment which enables concurrent message sending from multiple connections to the system under test. Messages round trip times are measured in the tester application. In the evaluation processing delay into system is simulated and influence of delay to the average round trip time is analysed.

TiO2 photocatalytic inactivation under simulated solar light of bacterial consortia in domestic wastewaters previously treated by UASB, duckweed and facultative ponds

In this work, TiO2 photocatalysis was used to disinfect domestic wastewaters previously treated by different biological treatment systems: Upward-flow Anaerobic Sludge Blanket (UASB), facultative pond, and duckweed pond. The microorganisms monitored were E. coli, total coliforms, Shigella species, and Salmonella species. Photocatalytic experiments were carried out using two light sources: a solar simulator (UV intensity: 68-70 W m-2) and black-light lamps (BLL UV intensity: 17-20 W m-2). Samples were taken after each treatment stage. Results indicate that bacterial photocatalytic inactivation is affected by characteristics of the effluent, including turbidity, concentration of organic matter, and bacterial concentration, which depend of the type of biological pretreatment previously used.

Design and implementation of a multipurpose reactor for scale-up studies

In the theoretical part, the different polymerisation catalysts are introduced and the phenomena related to mixing in the stirred tank reactor are presented. Also the advantages and challenges related to scale-up are discussed. The aim of the applied part was to design and implement an intermediate-sized reactor useful for scale-up studies. The reactor setting was tested making one batch of Ziegler–Natta polypropylene catalyst. The catalyst preparation with a designed equipment setting succeeded and the catalyst was analysed. The analyses of the catalyst were done, because the properties of the catalyst were compared to the normal properties of Ziegler–Natta polypropylene catalyst. The total titanium content of the catalyst was slightly higher than in normal Ziegler–Natta polypropylene catalyst, but the magnesium and aluminium content of the catalyst were in the normal level. By adjusting the siphonation tube and adding one washing step the titanium content of the catalyst could be decreased. The particle size of the catalyst was small, but the activity was in a normal range. The size of the catalyst particles could be increased by decreasing the stirring speed. During the test run, it was noticed that some improvements for the designed equipment setting could be done. For example more valves for the chemical feed line need to be added to ensure inert conditions during the catalyst preparation. Also nitrogen for the reactor needs to separate from other nitrogen line. With this change the pressure in the reactor can be kept as desired during the catalyst preparation. The proposals for improvements are presented in the applied part. After these improvements are done, the equipment setting is ready for start-up. The computational fluid dynamics model for the designed reactor was provided by cooperation with Lappeenranta University of Technology. The experiments showed that for adequate mixing with one impeller, stirring speed of 600 rpm is needed. The computational fluid dynamics model with two impellers showed that there was no difference in the mixing efficiency if the upper impeller were pumping downwards or upwards.

Flow injection spectrophotometric determination of adrenaline using a solid-phase reactor containing triiodide ions immobilized in an anion-exchange resin

A flow injection spectrophotometric procedure with on-line solid-phase reactor containing ion triiodide immobilized in an anion-exchange resin is proposed for the determination of adrenaline (epinephrine) in pharmaceutical products. Adrenaline is oxidized by triiodide ion immobilized in an anionic-exchange resin yielding adrenochrome which is transported by the carrier solution and detected at a wavelength of 488 nm. Adrenaline was determined in three pharmaceutical products in the 6.4 x 10-6 to 3.0 x 10-4 mol L-1 concentration range with a detection limit of 4.8 x 10-7 mol L-1. The recovery of this analyte in three samples ranged from 96.0 to 105 %. The analytical frequency was 80 determinations per hour and the RSDs were less than 1 % for adrenaline concentrations of 6.4 x 10-5 and 2.0 x 10-4 mol L-1 (n=10). A paired t-test showed that all results obtained for adrenaline in commercial formulations using the proposed flow injection procedure and a spectrophotometric batch procedure agree at the 95% confidence level.

Balanço de massa de reatores anaeróbicos de fluxo ascendente com manta de lodo (UASB) tratando águas residuárias de suinocultura

Foi obtido o balanço de massa, a partir dos valores médios das determinações de demanda química de oxigênio (DQO) e produção de metano (CH4), em dois reatores UASB de bancada com volume de 10,5 L tratando águas residuárias de suinocultura, submetidos a condições operacionais distintas no que diz respeito às concentrações de sólidos suspensos totais do afluente (SST de 500; 1.000; 1.500 e 2.000 mg L-1), tempo de detenção hidráulica (TDH de 30; 20; 12 e 8 h), taxas de carregamento orgânico volumétrico (TCOV de 0,8 a 8,0 kg DQO total (m³ d)-1) e temperatura (ambiente e controlada a 25º e 30ºC). Verificou-se que a DQO total removida convertida em CH4 variou de 28 a 51% e a relação DQO-CH4 por DQO dissolvida removida de 0,94 a 2,07; indicando alta participação da remoção física dos sólidos do afluente, de 49 a 72%, na remoção de DQO total nos reatores, a qual variou de 75 a 92%. A concentração de SST do afluente, a temperatura, o TDH e a TCOV influenciaram nesse desempenho dos reatores UASB.

Desempenho de processo anaeróbio em dois estágios (reator compartimentado seguido de reator UASB) para tratamento de águas residuárias de suinocultura

Avaliou-se o efeito das águas residuárias de suinocultura com concentrações de sólidos suspensos totais em torno de 6.000 mg L-1 (DQOtotal variando de 7.557 a 11.640 mg L-1) no desempenho de processo anaeróbio em dois estágios compostos por reator compartimentado (ABR) e reator de fluxo ascendente com manta de lodo (UASB), instalados em série, em escala-piloto (volumes de 530 e 120 L, respectivamente), submetidos a tempos de detenção hidráulica (TDH) de 56 a 18 h no primeiro reator e de 13 a 4 h no segundo reator. As eficiências médias de remoção de DQOtotal variaram de 71,1 a 87,5% no reator ABR e de 41,5 a 50,1% no reator UASB, resultando em valores médios de 86,8 a 94,9% para o sistema de tratamento anaeróbio em dois estágios com carga orgânica volumétrica (COV), na faixa de 5,05 a 10,12 kg DQOtotal (m³ d)-1, no reator ABR, e de 2,83 a 9,63 kg DQOtotal (m³ d)-1, no reator UASB. As eficiências de remoção de SST e SSV foram da ordem de 95,6%. O teor de metano no biogás manteve-se acima de 70% para os dois reatores. A produção volumétrica de metano máxima de 0,755 m³ CH4 (m³ d)-1 ocorreu no reator 1, com COV de 10,12 kg DQOtotal (m³ d)-1 e TDH de 18 h. Os valores médios de pH variaram na faixa de 7,2 a 8,0 para os efluentes dos reatores 1 e 2. Os ácidos voláteis totais mantiveram-se estáveis com concentrações abaixo de 200 mg L-1. Com variações abruptas e acentuadas de concentrações de SST e DQOtotal do afluente, os reatores mantiveram as eficiências de remoção de DQO e sólidos suspensos, em torno de 70%, e a qualidade do biogás, com 80% de CH4.

APROS model validation in case of fast transients in a boiling water reactor

This Master´s thesis investigates the performance of the Olkiluoto 1 and 2 APROS model in case of fast transients. The thesis includes a general description of the Olkiluoto 1 and 2 nuclear power plants and of the most important safety systems. The theoretical background of the APROS code as well as the scope and the content of the Olkiluoto 1 and 2 APROS model are also described. The event sequences of the anticipated operation transients considered in the thesis are presented in detail as they will form the basis for the analysis of the APROS calculation results. The calculated fast operational transient situations comprise loss-of-load cases and two cases related to a inadvertent closure of one main steam isolation valve. As part of the thesis work, the inaccurate initial data values found in the original 1-D reactor core model were corrected. The input data needed for the creation of a more accurate 3-D core model were defined. The analysis of the APROS calculation results showed that while the main results were in good accordance with the measured plant data, also differences were detected. These differences were found to be caused by deficiencies and uncertainties related to the calculation model. According to the results the reactor core and the feedwater systems cause most of the differences between the calculated and measured values. Based on these findings, it will be possible to develop the APROS model further to make it a reliable and accurate tool for the analysis of the operational transients and possible plant modifications.

Tratamento anaeróbio de águas residuárias do beneficiamento de café por via úmida em reatores UASB em dois estágios

Neste trabalho, avaliou-se a eficiência do tratamento de águas residuárias do beneficiamento de café por via úmida em reatores anaeróbios de fluxo ascendente com manta de lodo (UASB), em dois estágios, em escala de bancada, submetidos a tempos de detenção hidráulica (TDH) de 4,0; 5,2 e 6,2 dias e cargas orgânicas volumétricas (COV) de 5,8; 3,0 e 3,6 g DQO total (L d)-1, no primeiro reator (R1), e TDH de 2,0; 2,6 e 3,1 dias e COV de 5,8; 0,5 e 0,4 g DQO total (L d)-1, no segundo reator (R2). Os valores médios de DQO do afluente variaram de 15.440 a 23.040 mg O2 L-1. As eficiências médias de remoção de DQO total e SST foram de 66 a 98% e de 93 a 97%, respectivamente, nos reatores UASB, em dois estágios. O teor médio de metano no biogás variou de 69 a 89%, no reator R1, e de 52 a 73%, no reator R2. A produção volumétrica máxima de metano de 0,708 L CH4 (L reator d)-1 foi obtida com COV de 3,6 g DQO (Ld)-1 e TDH de 6,2 d, no reator R1. Os valores médios de pH variaram de 4,7 a 7,7 e de 4,9 a 8,0 nos efluentes dos reatores R1 e R2, respectivamente. As concentrações de ácidos voláteis totais nos efluentes mantiveram-se estáveis com valores inferiores a 100 mg L-1, com TDH de 5,2 e 6,2 dias, no reator R1, e TDH de 2,6 e 3,1 dias, no reator R2. As concentrações médias de fenóis totais no afluente variaram de 80 a 97 mg L-1 e as eficiências médias de remoção nos reatores UASB, em dois estágios, foram de 72 a 90%.

Remoção de matéria orgânica, de nutrientes e de coliformes no processo anaeróbio em dois estágios (reator compartimentado seguido de reator UASB) para o tratamento de águas residuárias de suinocultura

Neste trabalho, avaliou-se o efeito das águas residuárias de suinocultura, com concentrações médias de sólidos suspensos totais variando de 4.591 a 13.001 mg L-1, no desempenho de processo anaeróbio, em dois estágios, compostos por reator compartimentado (ABR) e reator de fluxo ascendente com manta de lodo (UASB), instalados em série, em escala- -piloto (volumes de 530 e 120 L, respectivamente), submetidos a tempos de detenção hidráulica (TDH) de 60; 36 e 24 h no primeiro reator, e de 13,6; 8,2 e 5,4 h no segundo reator. As eficiências médias de remoção de DQOtotal variaram de 69 a 84% no reator ABR e de 39 a 58% no reator UASB, resultando em valores médios de 87 a 94% para o sistema de tratamento anaeróbio em dois estágios, com carga orgânica volumétrica (COV) na faixa de 11,5 a 18,0 g DQOtotal (L d)-1 no reator ABR, e de 4,2 a 13,4 g DQOtotal (L d)-1 no reator UASB. A produção volumétrica máxima de metano de 0,227 m³ CH4 (m³ reator d)-1 ocorreu no reator UASB, com COV de 10,6 g DQOtotal (L d)-1 e TDH de 5,4 h. As maiores eficiências de remoção de coliformes totais e termotolerantes (99,7%), DQOdiss (94%), SST (96%), NTK (71%), P-total (61%) e outros nutrientes, no sistema de tratamento anaeróbio em dois estágios, foram obtidas com o TDH de 73,6 h e temperatura climatológica média de 24,6 °C, aplicando-se a menor COV (de 11,5 g DQOtotal (L d)-1 no reator ABR, e de 4,2 g DQOtotal (L d)-1 no reator UASB) com a maior concentração de SST do afluente (13.001 mg L-1).

Tratamento de águas residuárias de suinocultura em reatores anaeróbios de fluxo ascendente com manta de lodo (uasb) em dois estágios seguidos de reator operado em batelada sequencial (RBS)

Neste trabalho, avaliou-se o desempenho de dois reatores anaeróbios de fluxo ascendente com manta de lodo (UASB), em série, seguidos de um reator operado em batelada sequencial (RBS) com etapa aeróbia, no tratamento de águas residuárias de suinocultura. O sistema de tratamento anaeróbio em dois estágios foi alimentado com águas residuárias de suinocultura com concentrações médias de sólidos suspensos totais (SST), de 4.427 a 16.425 mg L-1 . As cargas orgânicas volumétricas (COV) aplicadas no reator UASB do primeiro estágio variaram de 14,8 a 24,4 g DQO (L d)-1. Os tempos de detenção hidráulica (TDH) foram de 28 e 11 h e de 14 e 6 h no primeiro e segundo reatores UASB, respectivamente. O RBS foi operado com 1 e 2 ciclos diários de alimentação e com concentrações de SST do afluente, de 1.348 a 2.036 mg L-1 . As maiores eficiências de remoção de DQOtotal ocorreram com os maiores TDH, com valores médios de 78 a 88% nos reatores UASB, em dois estágios. Com o tratamento do efluente dos reatores UASB no RBS, as eficiências médias de remoção aumentaram para 93 a 97%, 92 a 98%, 57 a 78%, 71 a 88% e 68 a 85% para a DQO total, SST, P-total, nitrogênio total Kjeldahl (NTK) e nitrogênio total (NT), respectivamente. Para os coliformes termotolerantes, as remoções foram de 93,80 a 99,99%.

Kinetic behavior of nitrification in the post-treatment of poultry wastewater in a sequential batch reactor

A sequential batch reactor with suspended biomass and useful volume of 5 L was used in the removal of nutrients and organic matter in workbench scale under optimal conditions obtained by central composite rotational design (CCRD), with cycle time (CT) of 16 h (10.15 h, aerobic phase, and 4.35 h, anoxic phase) and carbon: nitrogen ratio (COD/NO2--N+NO3--N) equal to 6. Complete cycles (20), nitrification followed by denitrification, were evaluated to investigate the kinetic behavior of degradation of organic (COD) and nitrogenated (NH4+-N, NO2--N and NO3--N) matter present in the effluent from a bird slaughterhouse and industrial processing facility, as well as to evaluate the stability of the reactor using Shewhart control charts of individual measures. The results indicate means total inorganic nitrogen (NH4+-N+NO2- -N+NO3--N) removal of 84.32±1.59% and organic matter (COD) of 53.65±8.48% in the complete process (nitrification-denitrification) with the process under statistical control. The nitrifying activity during the aerobic phase estimated from the determination of the kinetic parameters had mean K1 and K2 values of 0.00381±0.00043 min-1 and 0.00381±0.00043 min-1, respectively. The evaluation of the kinetic behavior of the conversion of nitrogen indicated a possible reduction of CT in the anoxic phase, since removals of NO2--N and NO3--N higher than 90% were obtained with only 1 h of denitrification.