888 resultados para sodium hydroxide
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Master Thesis to obtain the Master degree in Chemical Engineering - Branch Chemical Processes
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Nesta dissertação pretendeu-se estudar a viabilidade do uso de eletrodiálise com membranas bipolares (BM) na recuperação de ácido clorídrico e de hidróxido de sódio a partir de um efluente industrial que contém 1.4 mol/L de cloreto de sódio. Estas membranas mostraram ser uma ferramenta eficiente para a produção de ácidos e bases a partir do respetivo sal. Foi feita uma seleção de diferentes membranas bipolares (Neosepta, Fumatech e PCA) e aniónicas (PC-SA e PC-ACID 60) na tentativa de encontrar a combinação mais adequada para o tratamento do efluente. Dependendo do critério, o melhor arranjo de membranas é o uso de PC-ACID 60 (membrana aniónica), PC-SK (membrana catiónica) e membranas bipolares do tipo Neosepta para maior pureza dos produtos; membranas bipolares Fumatech para maior eficiência de dessalinização e membranas bipolares PCA para um maior grau de dessalinização. Tecnologicamente foi possível obter uma dessalinização de 99.8% em quatro horas de funcionamento em modo batch com recirculação de todas as correntes. Independentemente da combinação usada é recomendável que o processo seja parado quando a densidade de corrente deixa de ser máxima, 781 A/m2. Assim é possível evitar o aumento de impurezas nos produtos, contra difusão, descida instantânea do pH e uma dessalinização pouco eficiente. A nível piloto o principal fornecedor de membranas e unidade de tratamento “stack” é a marca alemã PCA. Sendo assim realizaram-se ensaios de repetibilidade, contra difusão, avaliação económica e upscaling utilizando as membranas bipolares PCA. A nível económico estudou-se o uso de dois tipos de unidades de tratamento; EDQ 380 e EDQ 1600, para diferentes níveis de dessalinização (50, 75 e 80%). Tendo em conta a otimização económica, é recomendável uma dessalinização máxima de 80%, uma vez que a eficiência de processo a este ponto é de 40%. A aplicação do método com a unidade EDQ 1600 para uma dessalinização de 50% é a mais vantajosa economicamente, com custos de 16 €/m3 de efluente tratado ou 0,78 €/kg Cl- removido. O número de unidades necessárias é 4 posicionados em série.
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The purpose of this study was to evaluate the influence of variables in a flotation technique for the recovery of Toxocara canis eggs from soil. The trials were done under standardized conditions on one gram of previously sterilized soil samples contaminated with 200 eggs of T. canis. The following variables were evaluated in serial steps: sieving; type of wash; time of stirring; resuspension of sediment; solution flotation. Centrifuge-flotation in sodium nitrate (d = 1.20 g/cm³) was adopted as an initial technique, using Tween 80 (0.2%) and decinormal sodium hydroxide as solutions for washing the samples. Ten tests were done to compare the variables, using counting in triplicate. The sieving of the material reduced significantly the recovery of eggs (p < 0.001) and the number of eggs recovered was higher when the sediment was resuspended (p < 0.05). After standardization, flotation solutions sodium chloride, zinc sulfate, sodium dichromate, magnesium sulfate, and sodium nitrate (d = 1.20g/cm³) were compared. The best results were obtained by using zinc sulfate solution. In conclusion, the chances of recovering T. canis eggs from samples using flotation solutions can be increased by washing of soil twice using distilled water, and resuspension of sediment. On the other hand, the sieving procedure can drastically reduce the number of eggs.
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In recent years there has been a growing interest in developing news solutions for more ecologic and efficient construction, including natural, renewable and local materials, thus contributing in the search for more efficient, economic and environmentally friendly construction. Several authors have assessed the possibility of using various agricultural sub products or wastes, as part of the effort of the scientific community to find alternative and more ecologic construction materials. Corn cob is an agricultural waste from a very important worldwide crop. Natural glues are made from natural materials, non-mineral, that can be used as such or after some modifications to achieve the behaviour and performance required. Two examples of these natural glues are casein and wheat flour-based glues that were used in the present study. Boards with different compositions were manufactured, having as variables the type of glue, the dimension of the corn cob particles and the features of the pressing process. The tests boards were characterized with physical and mechanical tests, such as thermal conductivity (λ) with a ISOMET 2104 and 60 mm diameter contact probe, density (ρ) based on EN 1602:2013, surface hardness (SH) with a PCE Shore A durometer, surface resistance (SR) with a PROCEQ PT pendular sclerometer, bending behaviour (σ) based on EN 12089:2013, compression behaviour (σ10) based on EN 826:2013 and resilience (R) based on EN 1094-1:2008, with a Zwick Rowell bending equipment with 2 kN and 50 kN load cells (Fig. 1), dynamic modulus of elasticity (Ed) with a Zeus Resonance Meter equipment (Fig. 5) based on NP EN 14146:2006 and water vapour permeability (δ) based on EN 12086:2013. The various boards produced were characterized according to the tests and the ones with the best results were C8_c8 (casein glue, grain size 2,38-4,76 mm, cold pressing for 8 hours), C8_c4 (casein glue, grain size 2,38-4,76 mm, cold pressing for 4 hours), F8_h0.5 (wheat flour glue, grain size 2,38-4,76 mm, hot pressing for 0,5 hours), FEV8_h0.5 (wheat flour, egg white and vinegar glue, grain size 2,38-4,76 mm, hot pressing for 0,5 hours) and FEVH68_c4 (wheat flour, egg white, vinegar and 6 g of sodium hydroxide glue, grain size 2,38-4,76 mm, cold pressing for 4 hours). Taking into account the various boards produced and respective test results the type of glue and the pressure and pressing time are very important factors which strongly influence the final product. The results obtained confirmed the initial hypotheses that these boards have potential as a thermal and, eventually, acoustic insulation material, to use as coating or intermediate layer on walls, floors or false ceilings. This type of board has a high mechanical resistance when compared with traditional insulating materials.The integrity of these boards seems to be maintained even in higher humidity environments. However, due to biological susceptibility and sensitivity to water, they would be more adequate for application in dry interior conditions.
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This work reports the development of field-effect transistors (FETs), whose channel is based on zinc oxide (ZnO) nanoparticles (NPs). Using screen-printing as the primary deposition technique, different inks were developed, where the semiconducting ink is based on a ZnO NPs dispersion in ethyl cellulose (EC). These inks were used to print electrolyte-gated transistors (EGTs) in a staggered-top gate structure on glass substrates, using a lithium-based polymeric electrolyte. In another approach, FETs with a staggered-bottom gate structure on paper were developed using a sol-gel method to functionalize the paper’s surface with ZnO NPs, using zinc acetate dihydrate (ZnC4H6O4·2H2O) and sodium hydroxide (NaOH) as precursors. In this case, the paper itself was used as dielectric. The various layers of the two devices were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier Transform Infrared spectroscopy (FTIR), thermogravimetric and differential scanning calorimetric analyses (TG-DSC). Electrochemical impedance spectroscopy (EIS) was used in order to evaluate the electric double-layer (EDL) formation, in the case of the EGTs. The ZnO NPs EGTs present electrical modulation for annealing temperatures equal or superior to 300 ºC and in terms of electrical properties they showed On/Off ratios in the order of 103, saturation mobilities (μSat) of 1.49x10-1 cm2(Vs)-1 and transconductance (gm) of 10-5 S. On the other hand, the ZnO NPs FETs on paper exhibited On/Off ratios in the order of 102, μSat of 4.83x10- 3 cm2(Vs)-1and gm around 10-8 S.
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In search to increase the offer of liquid, clean, renewable and sustainable energy in the world energy matrix, the use of lignocellulosic materials (LCMs) for bioethanol production arises as a valuable alternative. The objective of this work was to analyze and compare the performance of Saccharomyces cerevisiae, Pichia stipitis and Zymomonas mobilis in the production of bioethanol from coconut fibre mature (CFM) using different strategies: simultaneous saccharification and fermentation (SSF) and semi-simultaneous saccharification and fermentation (SSSF). The CFM was pretreated by hydrothermal pretreatment catalyzed with sodium hydroxide (HPCSH). The pretreated CFM was characterized by X-ray diffractometry and SEM, and the lignin recovered in the liquid phase by FTIR and TGA. After the HPCSH pretreatment (2.5% (v/v) sodium hydroxide at 180 °C for 30 min), the cellulose content was 56.44%, while the hemicellulose and lignin were reduced 69.04% and 89.13%, respectively. Following pretreatment, the obtained cellulosic fraction was submitted to SSF and SSSF. Pichia stipitis allowed for the highest ethanol yield 90.18% in SSSF, 91.17% and 91.03% were obtained with Saccharomyces cerevisiae and Zymomonas mobilis, respectively. It may be concluded that the selection of the most efficient microorganism for the obtention of high bioethanol production yields from cellulose pretreated by HPCSH depends on the operational strategy used and this pretreatment is an interesting alternative for add value of coconut fibre mature compounds (lignin, phenolics) being in accordance with the biorefinery concept.
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For the determination of exchangeable hydrogen ion in soils, the authors of the presente work made the extraction with normal calcium acetate solution that may have an initial pH between 7 and 8 without altering the amount of hydrogen ion extracted. The extraction was made by shaking 5,0 grams of air dry soil with 100 ml of normal calcium acetate solution, the pH of wich was ascertained to 7,0, 7,5 and 8,0 with acetic acid, in 250 mil conical flasks for 30 minutes in a Wagner shaker (30-40 rpm). The contents of the flasks were then, filtered. A 50 ml aliquot of each of the leachate was titrated with a 0,020 N NaOH solution and the volumes consumed sodium hydroxide were ploted against pH. The titration curves thus obtained showed to be straight lines between pH 8 and 9 and parallel to the curve obtained by the titration of the blank. Two ways of locating the end point of the titration showed to be possible: the use of a pHmeter or titrimeter or the use of phenolphtalein as indicator. When using a pH meter or a titrimeter, the end point may rest in any point between pH 8 and 9, and the volume of sodium hydroxide consumed is found by comparison with a similar curve obtained by the titration of the blank. When using phenolphtalein the calcium acetate solution must have a pH below 8.
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A chemical test previously described for the diagnosis of pregnancy was applied to the study of the excretion of gonadotropin in the urine during menstrual cycle. The chemical test is based on the selective adsorption by kaolim of the reducing substances biologically related to urinary gonadotropin. The active substance when acidified to pH 4.0 is adsorbed by the kolin and eluated with O.1N sodium hydroxide. The alkaline solution is treated by Somogyi's copper reagent and the excess not reduced is titrated by 0.005 N sodium thiosulfate. Gonadotropin is quantitatively addorbed by kaolin at pH 4.0 and eluated by alkaline solution as previously demonstrated by the A. (1). In the present paper the complete menstrual cycle was studied daily. It was observed that normally there are two distinct maxima of excretion. This study is based on 11 normal cycles (24-30 days) and 34 abnormal ones. Normal cycles showed a intramenstrual estrogens elimination from 200 to 260 mice units determinated by the Allen - Doisy full estrus smear test. The abnormal cycles belonging also to normal women showed much less estrogen excretion (14 to 25 mice units) Table II). In those cases with decreased estrogen excretion no fall in the curve after 14 th. day was observed. The A. suggest that the peaks of gonadotropin excretion is not related to the oculation but possibly due, the first one, to the follicle stimulating hormone and the second to the luteinizing hormone of hormone stimulating of the inerstitial tissue.
Design of a Control Slide for Cyanoacrylate Polymerization : Application to the CA-Bluestar Sequence
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Casework expercience has shown that, in some cases, long exposures of surfaces subjected to cyanoacrylate (CA) fuming had detrimental effects on the subsequent application of Bluestar. This study aimed to develop a control mechanism to monitor the amount of CA deposited prior to the subsequent treatment. A control slide bearing spots of sodium hydroxide (NaOH) of known concentrations and volume was designed and validated against both scanning electron microscopy (SEM) observations and latent print examiners' assessments of the quality of the developed marks. The control slide allows one to define three levels of development that were used to monitor the Bluestar reaction on depleting footwear marks left in diluted blood. The appropriate conditions for a successful application of both CA and Bluestar were determined.
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In this study, glyoxalated alkaline lignins with a non-volatile and non-toxic aldehyde, which can be obtained from several natural resources, namely glyoxal, were prepared and characterized for its use in wood adhesives. The preparation method consisted of the reaction of lignin with glyoxal under an alkaline medium. The influence of reaction conditions such as the molar ratio of sodium hydroxide-to-lignin and reaction time were studied relative to the properties of the prepared adducts. The analytical techniques used were FTIR and 1H-NMR spectroscopies, gel permeation chromatography (GPC), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). Results from both the FTIR and 1H-NMR spectroscopies showed that the amount of introduced aliphatic hydroxyl groups onto the lignin molecule increased with increasing reaction time and reached a maximum value at 10 h, and after they began to decrease. The molecular weights remained unchanged until 10 h of reaction time, and then started to increase, possibly due to the repolymerization reactions. DSC analysis showed that the glass transition temperature (Tg) decreased with the introduction of glyoxal onto the lignin molecule due to the increase in free volume of the lignin molecules. TGA analysis showed that the thermal stability of glyoxalated lignin is not influenced and remained suitable for wood adhesives. Compared to the original lignin, the improved lignin is reactive and a suitable raw material for adhesive formula
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The behavior of stone groundwood / polypropylene injection-molded composites was evaluated with and without coupling agent. Stone groundwood (SGW) is a fibrous material commonly prepared in a high yield process and mainly used for papermaking applications. In this work, the use of SGW fibers was explored as a reinforcing element of polypropylene (PP) composites. The surface charge density of the composite components was evaluated, as well as the fiber’s length and diameter inside the composite material. Two mixing extrusion processes were evaluated, and the use of a kinetic mixer, instead of an internal mixer, resulted in longer mean fiber lengths of the reinforcing fibers. On the other hand, the accessibility of surface hydroxyl groups of stone groundwood fibers was improved by treating the fibers with 5% of sodium hydroxide, resulting in a noticeable increase of the tensile strength of the composites, for a similar percentage of coupling agent. A new parameter called Fiber Tensile Strength Factor is defined and used as a baseline for the comparison of the properties of the different composite materials. Finally the competitiveness of stone groundwood / polypropylene / polypropylene-co-maleic anhydride system, which compared favorably to sized glass-fiber / polypropylene GF/PP and glass-fiber / polypropylene / polypropylene-co-maleic anhydride composite formulations, was quantified by means of the fiber tensile strength factor
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Knowledge of the soil physical properties, including the clay content, is of utmost importance for agriculture. The behavior of apparently similar soils can differ in intrinsic characteristics determined by different formation processes and nature of the parent material. The purpose of this study was to assess the efficacy of separate or combined pre-treatments, dispersion methods and chemical dispersant agents to determine clay in some soil classes, selected according to their mineralogy. Two Brazilian Oxisols, two Alfisols and one Mollisol with contrasting mineralogy were selected. Different treatments were applied: chemical substances as dispersants (lithium hydroxide, sodium hydroxide, and hexametaphosphate); pre-treatment with dithionite, ammonium oxalate, and hydrogen peroxide to eliminate organic matter; and coarse sand as abrasive and ultrasound, to test their mechanical action. The conclusion was drawn that different treatments must be applied to determine clay, in view of the soil mineralogy. Lithium hydroxide was not efficient to disperse low-CEC electropositive soils and very efficient in dispersing high-CEC electronegative soils. The use of coarse sand as an abrasive increased the clay content of all soils and in all treatments in which dispersion occurred, with or without the use of chemical dispersants. The efficiency of coarse sand is not the same for all soil classes.
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Tehokkain tapavalkaista mekaanisesti kuidutettua puumassaa on suorittaa se hapettavasti peroksidikemikaalilla vahvasti alkalisissa oloissa. Perinteisesti alkalisuus on aikaansaatu natriumhydroksidin ja -silikaatin avulla. Se kuitenkin liuottaa massasta merkittävästi ligniiniä, mikä huonontaa saantoa ja suurentaa valkaisun jätevesien orgaanisen hiilen määrää sekä kemiallista hapenkulutusta. Yhä kovenevien vaaleustavoitteiden ja tiukentuneen vedenkäytön seurauksena on syntynyt tarve etsiä parempia valkaisun alkaleja. Kirjallisuuden pohjalta valittiinkokeellisesti tutkittaviksi alkaleiksi magnesiumhydroksidi, magnesiumoksidi, kalsiumhydroksidi sekä kalsiumoksidi. Niiden toimivuutta hapettavan vetyperoksidivalkaisun alkaleina tutkittiin valkaisukokein natriumsilikaattilisäyksen kanssa sekä ilman. Näistä parhaiten toimivaksi osoittautui Mg(OH)2. Sen avulla suoritettiin jatkoksi laboratoriokoevalkaisuja korkeassa sakeudessa. Keski- ja korkeasakeusvalkaisukokeiden tulosten mukaan käytettäessä Mg(OH)2 -alkalia natriumydroksidin ja -silikaatin asemesta jää massan loppuvaaleus noin yhden ISO-prosentin verran heikommaksi. Tällöin valkaisusuodoksessa oli vain varsin vähäinen määrä massasta liuennutta orgaanista hiiliainesta, noin 45 % siitä, mitä natriumin yhdisteiden käyttö vertailukokeessa tuotti. Tulosta varmennettiin suorittamalla korkea-sakeusvalkaisukokeita hiokemassatehtaan olosuhteissa, massoilla ja kiertovesillä.Myös tehdaskokeiden mukaan valkaistun massan loppuvaaleus jää noin yhden ISO-prosentin alhaisemmaksi, mutta valkaisusuodoksen orgaanisen hiilen määrä (TOC) jääalle puoleen Na-kemikaalein suoritetusta vertailukokeesta.
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Työssä haettiin optimaalista valkaisukemikaalien annostelusuhdetta mahdollisimman vaalean massan valmistamiseksi. Tarkoituksena oli myös selvittää käytettävän tehdasprosessin pullonkauloja ja esittää vaihtoehtoja prosessin kehittämiseksi. Kirjallisuusosassa tutustuttiin mekaanisen massan peroksidivalkaisuun ja erilaisiin prosessimalleihin sen suorittamiseksi. Kirjallisuudesta saatuja lähtötietoja sovellettiin sitten ensin laboratorio- ja laajemmin tehdaskokein käytäntöön. Laboratoriokokeissa haettiin optimaalista lipeäannosta vakioperoksidiannoksella. Lisäksi selvitettiin lämpötilan ja viipymäajan vaikutusta valkaisutulokseen. Tuloksista oli todettavissa, että sekä lämpötilan että lipeäannoksen kasvattaminen kiihdyttää valkaisureaktiota. Korkeammassa lämpötilassa tarvittava lipeäannos on pienempi. Lyhyellä viipymäajalla ja matalammalla lämpötilalla saavutetaan hyviä tuloksia vain suurella lipeäannoksella. Suurempaa silikaattiannosta käytettäessä valkaisun jälkeen mitattu loppupH oli korkeampi ja jäännösperoksidin määrä hieman suurempi kuin referenssipisteessä. Vaaleudessa ei merkittävää muutosta näkynyt. Yleisesti laboratoriokokeiden tulokset vastasivat kirjallisuudessa esitettyjä tuloksia. Tehdaskokeet suoritettiin kahdella peroksidiannoksella. Kummallekin peroksidiannokselle haettiin optimaalinen lipeäannos. Lisäksi seurattiin silikaattiannoksen vaikutusta syntyvään vaaleuteen. Varsinaisten kokeiden lisäksi suoritettiin lyhyt maksimivaaleuskoe suurella peroksidiannoksella käyttäen kahta eri lipeäannosta. Suurin mitattu vaaleus oli 79,3 % ISO. Peroksidiannoksella 2,5 % saavutettiin noin 14 ISO-yksikön vaaleudennousu, ja annoksella 3 % vaaleudennousu oli noin 16 yksikköä. Tehdaskokeiden aikana kokeiltiin myös kemikaalien laimennusveden määrän vaikutusta vaaleuteen. Veden määrän vähetessä valkaisusakeus nousi ja vaaleus parani. Hiomon nykyprosessille laadittiin aine- ja energiatase. Taseet tehtiin myös prosessille, jossa nykyvalkaisimoon on lisätty valkaistun massan pesu ja jäännöskemikaalien kierrätys. Taseiden tarkoituksena oli selvittää virtaavien jakeiden määriä ja prosessin energiatasapainoa eri tilanteissa. Massan puhtauden paranemista pesun aikana tarkasteltiin laskennallisesti. Tämän työn aikana kävi selväksi, että oikeilla valkaisukemikaalisuhteilla pystytään valmistamaan vaaleaa massaa. Viipymäaikaa lisäämällä valkaisuun saisi lisää tehoa, mutta vain tunnin viipymäajalla päästään jo hyviin tuloksiin. Vaaleusheittoja aiheuttavat valkaistavan massan lähtövaaleuden, sakeuden ja lämpötilan muutokset. Lisäksi viipymäajan muutokset aiheuttavat huojuntaa saavutettavaan loppuvaaleuteen.
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Nykypäivänä ympäristön suojelu ja erityisesti jätevesipäästöjen pienentäminen vaikuttavat yhä enemmän metsäteollisuuden toimintatapoihin. Lisäksi veden käytön vähentyessä ja prosesseja suljettaessa silikaatteihin väistämättä liittyvät saostumat ovat kasvava ongelma. Magnesiumhydroksidin on havaittu olevan potentiaalinen natriumhydroksidin korvaava alkali mekaanisen massan peroksidivalkaisussa. Lisäksi magnesiumhydroksidilla voidaan saavuttaa lähes yhtä korkea vaaleus, jopa ilman silikaattia, kuin natriumhydroksidilla natriumsilikaatin kanssa. Magnesiumhydroksidin orgaanista ainesta liuottava vaikutus on myös noin puolet verrattuna natriumhydroksidiin. Työssä selvitettiin, miten häiriöaineet vaikuttavat mekaanisen massan peroksidivalkaisuun käytettäessä magnesiumhydroksidialkalia. Laboratoriokokeiden tulokset osoittivat, että magnesiumhydroksidi kesti paremmin valkaisussa käytettyjä häiriöaineita. Pienillä metallilisäyksillä ei ole vaikutusta massan vaaleuteen käytettäessä magnesiumhydroksidia. Korvattaessa laimennusvettä viirapuristimen suodoksella peroksidi kului lähes loppuun käytettäessä natriumhydroksidia, mikä näkyi myös vaaleuden heikkenemisenä. Valkaisukokeiden perusteella magnesiumhydroksidialkalilla jäädään jopa kolme prosenttiyksikköä natriumhydroksidin kanssa saadusta vaaleudesta, peroksidiannoksen olleessa kolme prosenttia. Mutta käytettäessä magnesiumhydroksidialkalia liuenneen orgaanisen hiilen kokonaismäärä (TOC) sekä biologinen (BOD7) että kemiallinen (CODcr) hapenkulutus pienenivät lähes puolella.