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The thesis entitled “New Supramolecular Ion Sensing Probes and their Application in the Detection of Environmentally Relevant Ions” deals with the design and synthesis of several small molecular probes which can specifically sense environmentally relevant ions of (anion or cation) particularly in aqueous or biological medium. The probes have been designed using four different molecular entities which include anthraquinone, oxidized bis-indolyl system, pyrene and rhodamine. The probes afford naked eye detection of a particular ion in the aqueous medium. This work has been divided into six chapters. Chapter 1. Introduction The first chapter gives a brief idea of ion sensor. It provides the description of various approaches used for designing molecular sensors. The chapter further presents an overview of the four different dyes (anthraquinone, oxidized-bis-indole, pyrene and rhodamine) used for designing probes in this work. The properties of these probes, their advantages and disadvantages to use as a signaling subunit have been discussed. This chapter also describes the use of micellar medium for solubilizing different organic dyes in water. Chapter 2. Colorimetric Probes based on Anthraimidazolediones for Selective Sensing of Fluoride and Cyanide ion via Intramolecular Charge Transfer. The second chapter describes the design and synthesis of four different probes based on anthra [1, 2-d] imidazole-6, 11-dione. The anthraquinone part of each molecule has an acceptor moiety whereas substituted nitrogen linked aromatic unit forms the donor site. Each probe acted as strong colorimetric sensor for fluoride and cyanide ion detection and exhibited intramolecular charge transfer (ICT) band which showed significant red-shifts after addition of either the F¯ or CN¯ ion. One of the probes 2 showed selective colorimetric sensing for both cyanide and fluoride ions. In organic medium 2 showed selective color change with fluoride and cyanide, whereas in aqueous organic medium it showed a selective ratiometric response towards cyanide ion. The effect of anionic charge (on the donor moiety) on ICT has been discussed. Among the various donor moieties, the donor site having negative charges on them was found to disperse greater electron density on them. Figure 1. Molecular structures of the sensors Chapter 3 deals with chemodosimetric detection of cyanide ion in water using various oxidized bis-indole based compounds. Chapter 3A. A Chemodosimetric Probe based on a Conjugated and oxidized Bis¬ indolyl System for Selective Naked Eye Sensing of Cyanide ion in Water. The chapter 3A describes the design and synthesis of a new water-soluble bis-indolyl based probe, 5 which possesses two –COOH groups. This probe specifically reacted with the CN¯ ion in pure water at ambient temperature and produced a remarkable change in color from red to colorless. The mechanism of this process was investigated by NMR (1H, 13C and DEPT-135) spectroscopy, mass spectrometry and kinetic studies. The mechanism investigation showed that the cyanide ion reacts with the probe and removes the conjugation of the bis-indolyl moiety of the probe with that of the 4-substituted aromatic ring which renders the probe colorless. Taken together a plausible mechanism of the reaction was presented which showed to operate via a Michael type adduct formation under ambient conditions of pH and temperature in water. The probe gave a detection limit of 0.38 ppm for detection of cyanide ion in water. Figure 2. Molecular structure of the probe 5. Chapter 3B. Micelle Assisted ppb level Detection of Cyanide ion in Water by Chemodosimetry and Visual detection of the Endogenous Cyanide. The chapter 3B deals with the synthesis of a bis-indole based colorimetric probe 6. The probe showed selective detection of the cyanide ion in water at ppb level and a visible detection of endogenous cyanide from cassava (a major staple food in the developing world) by chemodosimetry. The cyanide ion binds with the probe 6 in a chemodosimetric fashion and follows pseudo first-order kinetics in water under appropriate conditions. It showed a highly sensitive detection of the cyanide ion in water with a detection limit of 0.33 ppm. The use of the micellar medium improved the detection limit drastically and a ppb level detection limit was achieved. The probe also showed the detection of the endogenously bound cyanide in cassava both visually and by spectrophotometer. Figure 3. Molecular structure of the probe 6. Chapter 3C. Ratiometric Cyanide ion probe in Water and for the detection of the Endogenously bound cyanide. Chapter 3C presents the synthesis of two new bis-indolyl (7 and 8) based probes for colorimetric detection of cyanide ion in pure water. Compound 8 showed a ratiometric response with cyanide in water and a visual detection of the endogenously bound cyanide ion in cassava. Using compound 8 the selective detection of the cyanide ion in water was achieved with a detection limit of ~ 17 ppb which is almost 13 times lower than the permitted limit as specified by EPA, United States. 7; R = H 8; R = -(OCH2CH2)3CH3 Figure 4. Molecular structures of the probes 1 and 2. Chapter 4 deals with the colorimetric and ratiometric detection of the Cu2+and Hg2+ions using different small synthetic molecular probes. Chapter 4A. Colorimetric Sensors for Ratiometric Detection of Copper and Mercury ions in Biological media and below ppm level in Water. The chapter 4A deals with the synthesis of two novel colorimetric probes (9, 10) using bispicolyl unit as the binding moiety and anthraimidazolediones and bis-indolyl system as a signaling sub-unit. Using the two sensors, Cu2+ion can be detected below the permitted limit (1.3 ppm) in both drinking water and at physiological pH 7.4. Sensor 9 can detect both Cu2+and Hg2+ in water with very low detection limit. It showed specific binding with Cu2+ at physiological pH 7.4 and in presence of serum albumins. Chemosensor 10 can be used for the specific detection of both Cu2+and Hg2in water as well as for the contamination in microorganisms. Figure 5. Molecular structure of the sensors 9 and 10. Chapter 4B. A New Molecular Probe for the Selective Sensing of Cu2+ and Hg2+ ions in Micellar Media and in Live ells.This chapter describes a synthesis of a novel bispicolyl based sensor 11 which can detect Cu2+ ion specifically in water medium and both Cu2+ and Hg2+ ions selectivelyin Brij-58 micellar medium. In micellar medium both the ions can be detected in the ppb level. Using fluorescence spectroscopy these two metal ions can be discriminated.The probe is also be useful for checking metal ion contamination in cellular samples. Figure 6. Molecular structure of the sensor 11. Chapter 4C. Rhodamine based Sensors for Cu2+ and Hg2+ ions in Water and in Biological media. The chapter 4C presents the synthesis and the sensing properties of the three positional isomers of the pyridine end of the rhodamine-pyridine compounds (12-14). The three isomers only differ in the position of nitrogen of the pyridine moiety. Sensor 12, which contains the pyridine nitrogen at the ortho-position showed selective sensing toward Cu2+ ion in both pure water and in buffered physiological media of pH 7.4. It gave a detection limit of ~13 ppb which is 100 times lesser than the EPA permitted limit. The other two sensors 13 and 14, which possessed the pyridine ends with the nitrogen atom at the meta- and the para- positions respectively showed the selective sensing of Hg2+ ion in water and did not show any interaction with the Cu2+ ion. Probes 2 and 3 showed ‘turn-on’ detection of Hg2+ ion both in the UV-vis and the fluorescence emission spectroscopy. Compound 2 and 3 showed a detection limit of ~ 9 and 4 ppb respectively. The NMR titration showed the change in color was due to the opening of the spirolactam ring of the rhodamine. The sensors can also be used for the detection of Cu2+ and Hg2+ ion in real life water samples and in the live cells. Figure 7. Molecular structure of the sensors 12, 13 and 14. Chapter 5. Ratiometric and ppb level Detection of Toxic Transition Metal ions using a Single Probe in Micellar media. This chapter describes the selective sensing of multiple ions using a single probe 15. The probe incorporates pyrene and pyridine as signaling and interacting moiety respectively. The sensor showed different responses towards different metal ions just by varying the medium of detection. In organic solvent (acetonitrile), the probe showed selective detection of Hg2+ ion. In water the fluorescence quenching was observed with three metal ions, Cu2+, Hg2+ and Ni2+. Further just by varying the surface charge of different micellar media, the probe showed selective interaction with Hg2+ ion in neutral micelles (Brij-58). However, in anionic micellar medium (SDS), the probe showed selective changes with both Cu2+ and Ni2+ in the UV-vis spectroscopy. The discrimination between these two ions was achieved by emission spectroscopy, where it showed selective quenching only with Cu2+. Thus using a single probe all the three metal ions Cu2+, Hg2+ and Ni2+ can be detected and discriminated just by varying the surface charge of the micellar medium. Figure 8. Molecular structure of the sensors 15. Chapter 6. Highly sensitive Rhodamine Based Dual Probes for the Visual detection of F¯ and Hg2+ ions in Water. This chapter deals with the design and synthesis of two new rhodamine based probes (16-17) which act as dual probes for the ppb level selective detection of Hg2+ and F¯ ions in water and at physiological pH 7.4. The two probes were synthesized by coupling tert-butyldiphenylsilyl (TBDPS) protected forms of 4-hydroxybenzaldehyde and 2, 4- dihydroxy benzaldehyde with rhodamine hydrazone. The F¯ ion detection is based on the desilylation of the probe, whereas the spirolactam ring opening leads to the detection of Hg2+ ion. The two probes gave turn-on detection of both Hg2+ and F¯ ion selectively in aqueous medium with the detection limit well below the EPA permitted limits. The probes showed detection of both the ions by dual mode with visibly different color and fluorescence under UV-lamp. The F¯ ion interacts with the silyl bond of probe and the cleavage results into yellow color whereas; the addition of Hg2+ ion to the probe solution opened the spirolactam ring and resulted into appearance of pink color. Figure 9. Molecular structure of the probes 16 and 17. (For structural formula pl see the abstract file)

Thesis (MScEng)--Stellenbosch University, 2012. / ENGLISH ABSTRACT: A 2 stage heap leach process to extract base and precious metals from the Platreef ore is currently being investigated industrially. A first stage bioleach is used to extract the base metals. In the 2nd stage, cyanide is used as the lixiviant at high pH to extract the platinum group metals and gold. By analogy with current gold recovery practices, the present study investigates the preferential and quantitative adsorption of precious metals (Pt, Pd, Rh and Au) over base metals (Cu, Ni and Fe) from an alkaline cyanide medium, by means of granular activated carbon. Experiments were designed statistically to optimise the process parameters using synthetic alkaline cyanide solutions close in composition to those expected from plant leach solutions. The statistical approach allowed the development of a reliable quantitative approach to express adsorption as a response variable on the basis of a number of experiments. A 2IV(7-2) fractional factorial design approach was carried out in a batch adsorption study to identify significant experimental variables along with their combined effects for the simultaneous adsorption of Pt(II), Pd(II), Rh(III) and Au(I). The adsorbent was characterized using SEM-EDX, and XRF. Precious metals adsorption efficiency was studied in terms of process recovery as a function of different adsorption parameters such as solution pH, copper, nickel, free cyanide ion, thiocyanate, initial precious metal (Pt, Pd, Rh and Au) ion and activated carbon concentrations. It was shown that adsorption rates within the first 60 minutes were very high (giving more than 90% extraction of precious metals) and thereafter the adsorption proceeds at a slower rate until pseudo-equilibrium was reached. Among the different adsorption parameters, at 95% confidence interval, nickel concentration had the most influential effect on the adsorption process followed by the adsorbent concentration. Adsorption of Ni was found to proceed at approximately the same rate and with the same recovery as the precious metals, showing a recovery of approximately 90% in two hours. The kinetics of Cu adsorption were slower, with less than 30% being recovered at the 120 minute period. This suggests that the co-adsorption of Cu can be minimised by shortening the residence time. Adsorption of Fe was found to be less than 5%, while the recovery of Rh was negligibly small. The effect of thiocyanate ion concentration was not as important as the effect of free cyanide ion concentration but still had some influence. The correlation among different adsorption parameters was studied using multivariate analysis. The optimum experimental conditions resulted in a solution with pH of 9.5, [Cu(I)] of 10 ppm, [Ni(II)] of 10 ppm, [CN ] of 132.44 ppm, [SCN ] of 98.95 ppm, [PMs] of 2.03 ppm and [AC] of 10 g/L. Under these conditions, predicted adsorption percentages of Pt, Pd and Au were approximately 98, 92 and 100%, at the level of 95% probability within two hours as an effective loading time. The negative values of ΔG° for all ions under optimum conditions indicate the feasibility and spontaneous nature of the adsorption process. Chemisorption was found to be the predominant mechanism in the adsorption process of Pt(II), Pd(II) and Au(I). Based on their distribution coefficients, the affinity of activated carbon for metal ions follows the selectivity sequence expressed below. Au(CN) > Pt(CN) > Pd(CN) > Ni(CN) > Cu(CN) Finally, it is important that additional research and development activities in the future should prove the economic viability of the process. Future work is also needed to investigate the adsorption of precious metals (PMs) by comparing the efficiencies and kinetics of adsorption when using sodium hydroxide (in this study) or lime, respectively, in order to control the pH. / AFRIKAANSE OPSOMMING: ʼn Tweefasige hooploogproses vir die ontginning van basis- en edelmetale van die Platrif-erts word tans industrieel ondersoek. ʼn Eerstefase-bioloog word gebruik om die basismetale te ontgin. In die 2de fase word sianied gebruik as die uitloog by hoë pH om die platinum-groepmetale en goud te ontgin. Na analogie van hedendaagse goudherwinningspraktyke het die huidige studie die voorkeur- en kwantitatiewe adsorpsie van edelmetale (Pt, Pd, Rh en Au) bo basismetale (Cu, Ni en Fe) vanuit ʼn alkaliese sianiedmedium met behulp van korrelrige geaktiveerde koolstof ondersoek. Eksperimente is op statistiese wyse ontwerp om die parameters van die proses te optimaliseer deur van sintetiese alkaliese sianiedoplossings wat in hulle samestelling nou ooreenstem met dié wat van oplossings van plant-loog verwag word, gebruik te maak. Die statistiese benadering het die ontwikkeling van ʼn betroubare kwantitatiewe benadering om adsorpsie as ʼn responsveranderlike op grond van ʼn aantal eksperimente uit te druk, moontlik gemaak. ʼn 2IV(7-2) -Fraksionele faktoriale ontwerp-benadering is tydens ʼn lot-adsorpsiestudie gevolg om beduidende eksperimentele veranderlikes tesame met hulle gekombineerde uitwerkings vir die gelyktydige adsorpsie van Pt(II), Pd(II), Rh(III) en Au(I) te identifiseer. Die adsorbeermiddel is met behulp van SEM-EDX en XRF gekenmerk. Adsorpsiedoeltreffendheid van edelmetale is bestudeer ten opsigte van proseskinetika en herwinning as ʼn funksie van verskillende adsorpsieparameters soos oplossing-pH, koper, nikkel, vry sianiedioon, tiosianaat, aanvanklike edelmetaal (Pt, Pd, Rh en Au)-ioon en geaktiveerde koolstofkonsentrasies. Daar is aangetoon dat adsorpsietempo‟s binne die eerste 60 minute baie hoog was (het meer as 90% ekstraksie van edelmetale opgelewer) en daarna het die adsorpsie teen ʼn stadiger tempo voortgegaan totdat pseudo-ekwilibrium bereik is. Onder die verskillende adsorpsieparameters, by 95%-vertroubaarheidsinterval, het nikkel-konsentrasie die grootste invloed op die adsorpsieproses gehad, gevolg deur konsentrasie van die adsorbeermiddel. Daar is bevind dat die adsorpsie van Ni teen nagenoeg dieselfde tempo en met dieselfde herwinning as die edelmetale voortgegaan het, wat ná twee uur ʼn herwinning van nagenoeg 90% getoon het. Die kinetika van Cu-adsorpsie was stadiger, met minder as 30% wat teen die 120-minute-tydperk herwin is. Dit dui daarop dat die ko-adsorpsie van Cu tot die minimum beperk kan word deur verkorting van die verblyftyd. Daar is bevind dat die adsorpsie van Fe minder as 5% is, terwyl die herwinning van Rh onbeduidend klein was. Die uitwerking van die konsentrasie van die tiosianaatione was nie so belangrik as die uitwerking van die konsentrasie van vry sianiedione nie maar het steeds ʼn mate van invloed gehad. Die korrelasie tussen verskillende adsorpsieparameters is met behulp van meerveranderlike analise bestudeer. Die optimale eksperimentele toestande het gelei tot ʼn oplossing met ʼn pH van 9.5, [Cu(I)] van 10 dpm, [Ni(II)] van 10 dpm, [CN] van 132.44 dpm, [SCN] van 98.95 dpm, [EM‟e] van 2.03 dpm en [AC] van 10 g/L. Onder hierdie toestande was die voorspelde adsorpsiepersentasies van Pt, Pd en Au nagenoeg 98, 92 en 100%, op die vlak van 95%-waarskynlikheid binne twee uur as ʼn doeltreffende laaityd. Die negatiewe waardes van ΔG° vir alle ione onder optimale toestande dui op die uitvoerbaarheid en spontane aard van die adsorpsieproses. Daar is bevind dat chemiesorpsie die deurslaggewende meganisme by die adsorpsieproses van Pt(II), Pd(II) en Au(I) is. Gebaseer op hulle distribusiekoeffisiënte volg die affiniteit van geaktiveerde koolstof vir metaalione die selektiwiteitsvolgorde soos hieronder voorgestel. Au(CN) > Pt(CN) > Pd(CN) > Ni(CN) > Cu(CN) Laastens, dit is belangrik dat addisionele navorsing en ontwikkelingsaktiwiteite in die toekoms die ekonomiese haalbaarheid van die proses bewys. Werk in die toekoms is nodig om die adsorpsie van edelmetale (EM‟e) te ondersoek deur vergelyking van die doeltreffendhede en kinetika van adsorpsie wanneer natriumhidroksied (in hierdie studie) of kalk, onderskeidelik, gebruik word ten einde die pH te beheer

Thesis (MEng)--Stellenbosch University, 2014. / ENGLISH ABSTRACT: The Platreef ore deposit, situated in the Bushveld Igneous Complex, is one of the world’s largest platinum group metal (PGM) resources. The mineralogy of this resource is, however, unique as it consists of complex PGM mineralization with mainly copper and nickel, at very low PGM grades. The PGMs are mainly present in the ore as slow floating refractory minerals resulting in marginal process economics when processing via traditional mill-float-smelt processes. A new process is currently being investigated to extract PGMs from low grade Platreef ore and concentrate using a sequential heap leach process entailing heap bioleaching and high temperature cyanide leaching. The heap bioleach extracts the base metals in an acidic sulphate medium using a mixed culture of mesophiles and thermophiles. After heap bioleaching, the heap will be reclaimed, rinsed and restacked for high temperature cyanide leaching where the cyanide liquor is directly heated via solar energy in panels. Platinum, palladium and gold are extracted during the cyanide leaching stage and then recovered from the pregnant liquor either by adsorption onto activated carbon or ion exchange resins. Final metal recovery will proceed by techniques such as electrowinning and precipitation. In this thesis, process options for the recovery of platinum group metals from cyanide solutions were identified with different flowsheet alternatives developed utilizing these options. Simulations were made for the different processing alternatives with the objective of finding the alternative flowsheet to maximise net present value. The various processing options were simulated, combining data from concurrent experimental studies and data reported in literature with kinetic adsorption models. This was combined with economic models to arrive at an optimum design for each flowsheet alternative. Seven different processing alternatives for the recovery of platinum group metals from cyanide solutions were developed and investigated. These included two different activated carbon flowsheets as well as five different ion exchange resin flowsheets. The flowsheets differ in the elution procedures as well as the use of single or multiple resins. The well-known Merrill Crowe precipitation process was investigated but was found to yield unsatisfactory results. In each alternative, the cyanide solution is sent to a SART (sulphidization, acidification, recycling and thickening) plant to remove copper, nickel and zinc from solution prior to upgrading by means of adsorption onto activated carbon or ion exchange resins and subsequent elution. The platinum group metals are recovered from the eluate by precipitation using an autoclave, producing a solid product consisting of base and precious metals, while gold is recovered by electrowinning. It was found that the overall performance of the resin-in-solution (RIS) flowsheets were superior to that of the carbon-in-solution (CIS) flowsheets, from an overall PGM recovery perspective and product grades. The superior adsorption kinetics and high selectivity of the resins for the PGMs resulted in excellent overall plant performances, with PGM extractions in excess of 97%. Gold extraction efficiencies with resins were found to be lower than those achieved in the CIS flowsheets, mainly due to the higher selectivity of the resins for the divalent platinum and palladium cyanide complexes and poor gold elution efficiencies. The gold concentrations in the feed streams to these processes were, however, very low, at only 8.5% of the total precious metal content. The overall precious metal recoveries of the RIS flowsheets were thus higher than the CIS flowsheets due to the superior PGM extractions. From the cost analyses performed it was found that the RIS flowsheets requires lower initial capital costs, almost 28% lower than that require for the CIS flowsheets, while the operating cost requirements were found to be ±10% lower. This, combined with the high overall precious metal extractions, resulted in the RIS flowsheets to achieve higher net present values than those of the CIS flowsheets over an assumed project life of 15 years. The optimum flowsheet proposed for the recovery of precious metals from cyanide leach solutions was a RIS flowsheet option that employed the Amberlite PWA 5 resin, capable of extracting platinum, palladium and gold from solution, with elution being performed with a zinc cyanide solution. This process option had the lowest capital and operating cost requirements while achieving similar overall precious metal recoveries as the other flowsheets. Economic analysis of this process yielded the highest net present value, with a 31% increase in the overall return on investment compared to the optimal CIS flowsheet. Based on this, it was concluded that resin technology would be the best process option for recovering precious metals from cyanide leach solutions, however, additional research is required as the current level of process development is only at a concept phase. / AFRIKAANSE OPSOMMING: Die Platrif-erts, geleë in die Bosveld Kompleks, is een van die wêreld se grootste platinum groep metaal (PGM) reserwes. Die mineralogie van hierdie reserwe is uniek en bestaan uit komplekse PGM mineralisasie met hoofsaaklik koper en nikkel, teen baie lae PGM inhoud. Die PGMe is hoofsaaklik teenwoordig in die erts as stadig drywende minerale en dit lei tot marginale ekonomiese uitsigte wanneer hierdie reserwe deur tradisionele metodes verwerk word. Tans word ʼn nuwe proses ondersoek om die PGMe vanuit lae graad Platrif-erts en konsentraat te ontgin deur gebruik te maak van ʼn sekwensiële hooploogproses wat uit ʼn bio-loog en hoë temperatuur sianied loog stappe bestaan. Die bio-loog stap is verantwoordelik vir die ontginning van die basis metale deur gebruik te maak van ʼn suur sulfaat medium bestaande uit ʼn gemengde kultuur van mesofiele en termofiele. Nadat die bio-hooploog stap voltooi is, word die hoop herwin, gewas en herpak vir die daaropvolgende hoë temperatuur sianied loog, waar die sianied oplossing direk verhit word deur die gebruik van son panele. Platinum, palladium en goud word tydens hierdie stap ontgin en kan dan herwin word vanuit die loog oplossing deur gebruik te maak van adsorpsie deur geaktiveerde koolstof of ioon-uitruilings harse. Finale metaal herwinning kan deur elektroplatering en presipitasie vermag word. In hierdie tesis word verskeie proses opsies vir die ontginning en herwinning van PGMe vanuit sianied loog oplossings ondersoek waarna verskeie proses vloei diagram alternatiewe ontwikkel is met die doel om die opsie te vind wat die hoogste netto ekonomiese waarde sal oplewer. Die verskillende opsies is gesimuleer deur gebruik te maak van eksperimentele data gepubliseer in die literatuur en dit te kombineer met kinetiese adsorpsie modelle. Dit was dan gekombineer met ekonomiese modelle om ʼn optimum ontwerp van elke proses te verkry. Sewe verskillende proses vloei diagramme vir die herwinning en ontginning van PGMe vanuit sianied loog oplossings is ontwikkel en ondersoek. Hierdie het twee verkillende geaktiveerde koolstof prosesse en vyf verskillende ioon-uitruilings hars prosesse beslaan. Die opsies het verskil van eluerings metodes en adsorpsie medium. Die alombekende Merrill Crowe presipitasie proses is ook ondersoek, maar daar is gevind dat hierdie proses oneffektiewe resultate oplewer met betrekking tot die herwinning van die drie edel metale. In elke alternatief word die sianied oplossing in ʼn SART proses verwerk, waar die basis metale herwin word, gevolg deur die opgradering van die edel metale d.m.v. geaktiveerde koolstof adsorpsie of ekstraksie m.b.v. ioon-uitruilings harse, gevolg deur eluering. Die PGMe word dan herwin vanuit die eluerings oplossing deur termiese degradering van die metaal sianied komplekse, wat ʼn hoë graad presipitaat lewer bestaande uit die basis en edel metale. Goud word herwin d.m.v. elektroplatering. Daar is bevind dat die algehele verrigting van die ioon-uitruilings hars opsies beter was as die van die geaktiveerde koolstof opsies, beide van ʼn algehele edel metaal herwinnings en produk suiwerheid perspektief. Die verhoogde adsorpsie kinetika en hoër PGM selektiwiteit van die harse het daartoe gelei dat uitstekende algehele PGM herwinning verkry is in hierdie opsies, meer as 97%. Goud ekstraksie deur die harse was laer as wat verkry was deur die geaktiveerde koolstof opsies, weens die hoër selektiwiteit van die harse vir die divalente platinum en palladium sianied komplekse en laer hars eluering effektiwiteit. Die goud konsentrasies in die voer strome na die prosesse was laag, en het sowat 8.5% van die totale edel metale uitgemaak, wat bygedra het tot die lae goud herwinning. Algeheel was die edel metaal herwinning van die hars prosesse beter as die van die koolstof prosesse a.g.v. die hoër PGM adsorpsie. Koste evaluerings van die verskillende vloeidiagramme het getoon dat die hars opsies laer kapitaal kostes benodig, omtrent 28% minder as die koolstof opsies, terwyl bedryfskostes omtrent 10% minder was. Dit het bygedra tot die feit dat die ioon-uitruiling hars opsies ʼn hoër algehele netto ekonomiese waarde oor ʼn projek leeftyd van 15 jaar sal hê, aangesien de PGM ekstraksie, en dus die jaarlikse inkomste, ook hoër was. Die algehele proses vloei diagram wat voorgestel is vir die herwinning van edel metale vanuit sianied loog oplossings is die hars opsie wat gebruik maak van die Amberlite PWA 5 hars, wat in staat is om platinum, palladium en goud terselfdertyd te absorbeer, gevolg deur die eluering van die hars deur die gebruik van ʼn sink sianied oplossing. Hierdie proses het die laagste kapitaal en bedryfskostes getoon terwyl algehele PGM herwinning om en by dieselfde was as al die ander opsies. Hierdie proses sal verder ʼn 31% verhoging in die opbrengs op belegging lewer in vergelyking met die optimum geaktiveerde koolstof opsie. Die algehele gevolgtrekking is dat hars tegnologie die beter opsie sal wees vir die herwinning van edel metale vanuit sianied loog oplossings. Addisionele navorsing is dus nodig om resultate te verbeter aangesien hierdie studie slegs op ʼn konsep fase benadering was.

The rotational microwave spectra of the three isotopes (^13CH_3^12C^15N, ^12CH_3^13C^15N, and ^13CH_3^13C^15N) of the methyl cyanide molecule in the v_8=3, v_8=2, v_7=1 and v_4=1 vibrational energy levels for the rotational components 1£J£5 (for a range of frequency 17-95 GHz.) were experimentally and theoretically examined. Rotational components in each vibration were measured to determine the mutual interactions in each vibration between any of the vibrational levels investigated. The method of isotopic substitution was employed for internal tuning of each vibrational level by single and double substitution of ^13C in the two sites of the molecule. It was found that relative frequencies within each vibration with respect to another vibration were shifted in a systematic way. The results given in this work were interpreted on the basis of these energy shifts. Large departure between experimentally measured and theoretically predicted frequency for the quantum sets (J, K=±l, ϑ=±1), Kϑ-l in the v_8=3 vibrational states for the ^13c and ^15N tagged isotopes of CH_3CN showed anomalous behavior which was explained as being due to Fermi resonance. Accidently strong resonances (ASR) were introduced to account for some departures which were not explained by Fermi resonance.

The two most common commercial copper baths are the acid sulfate copper bath and the alkaline cyanide copper bath. Alkaline copper baths are mostly used to coat parts with complex geometry and to avoid galvanic deposition when depositing a metal on a less noble substrate. Because of the toxicity of cyanide compounds, alternative baths have been developed using different complexing agents. The starting point of the present study is a cyanide-free strike bath developed for copper plating on Zamak substrates developed by the Institute for Technological Research of the State of São Paulo/ Brazil. The replacement of a raw material such as cyanide must be economically advantageous and technically feasible. Therefore, this study intended to propose an alternative to the treatment of liquid wastes from the mentioned bath, aiming at simultaneous water reclamation and chemicals recovery in a closed system. The electrodialysis membrane separation process was studied, using a laboratoryscale system operating with a synthetic solution simulating the rinsing waters from the HEDP-based bath. The feasibility of the technique was evaluated by analyzing operational parameters such as ion extraction, demineralization rate, concentration rate, current efficiency for each anionic specie and average energy consumption. Because HEDP is a chelating agent, the transport of Cu(II)-HEDP chelates through anion-exchange membranes was also evaluated by means of electrochemical methods. Chronopotentiometric and current-voltage curves were constructed for different model solutions containing the same compounds as the original bath. A relation between the presence of chelates in the solutions and the fixed ion exchange group could be established. Lastly, deposition tests were performed using electrolytes containing the recycled inputs and the characteristics of the coatings were analyzed. The results showed that an electrodialysis stack using strongly basic anion-exchange membranes was suitable to produce treated solutions and a concentrate containing the ions from the bath. The concentrate could be added to the copper bath to compensate eventual drag-out losses without affecting the quality of the coatings. Thus, the application of electrodialysis was shown to be a feasible alternative for recovering water and inputs from the evaluated solution, reducing the wastewater generation and saving natural resources. / Os dois banhos de cobre comerciais mais comuns são o banho ácido à base de sulfato e o banho alcalino à base de cianeto. Os banhos alcalinos são usados principalmente para recobrir peças com geometria complexa e para evitar a deposição por deslocamento galvânico quando se deposita um metal em um substrato menos nobre. Por causa da toxicidade dos compostos cianídricos, banhos alternativos vêm sendo desenvolvidos usando diferentes agentes complexantes. O ponto de partida do presente estudo é um banho toque isento de cianeto para deposição de cobre em substratos de Zamak, desenvolvido pelo Instituto de Pesquisas Tecnológicas / Brasil. A substituição de matérias-primas como o cianeto deve ser economicamente vantajosa e tecnicamente viável. Desta forma, este estudo pretendeu propor uma alternativa para o tratamento de resíduos líquidos do banho mencionado, visando à recuperação simultânea da água e das matérias-primas em um sistema fechado. Foi estudado o processo de separação por membranas de eletrodiálise, usando um sistema em escala laboratorial operando com uma solução sintética que simulava as águas de lavagem do banho à base de HEDP. A viabilidade da técnica foi avaliada por meio da análise de parâmetros operacionais, como a extração dos íons, a taxa de dessalinização, o percentual de concentração, a eficiência de corrente calculada para cada espécie iônica e o consumo médio de energia. Devido ao HEDP ser um agente quelante, o transporte de quelatos Cu(II)-HEDP através de membranas aniônicas foi avaliado por meio de métodos eletroquímicos. Curvas cronopotenciométricas e curvas corrente-potencial foram construídas para diferentes soluções sintéticas que continham os mesmos compostos que o banho original. A relação entre a presença de quelatos nas soluções e os grupos fixos de troca iônica pôde ser estabelecida. Por fim, testes de deposição foram realizados usando eletrólitos contendo os compostos reciclados e as características dos depósitos foram analisadas. Os resultados mostraram que o sistema de eletrodiálise usando membranas aniônicas contendo grupos de troca fortemente básicos pôde produzir soluções tratadas e um concentrado contendo os íons do banho. O concentrado pôde ser adicionado ao banho original para compensar eventuais perdas por arraste sem afetar a qualidade dos depósitos. Assim, a aplicação da eletrodiálise se mostrou uma alternativa viável para a recuperação de água e de insumos da solução avaliada, reduzindo a geração de efluentes e economizando recursos naturais.

Made available in DSpace on 2014-12-17T15:42:17Z (GMT). No. of bitstreams: 1 VeronicaSO_DISSERT.pdf: 3422406 bytes, checksum: d33eed82fa27aa7c5249e32ca3da7fd8 (MD5) Previous issue date: 2014-01-22 / Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior / The present work has as main objective to contribute to the coordination chemistry of the ligand kojic acid, with the synthesis and characterization of the homoleptic compounds [Al(kj)3], [Fe(kj)3], [Fe(kj)2], [Cu(kj)2] e [Ru(kj)3], and the new heteroleptic complexes, trans- K2[Fe(kj)2(CN)2] and trans-Na2[Ru(kj)2(CN)2]. The obtained compounds were characterized by vibrational spectroscopy in the infrared region (IV) and Electronic spectroscopy in the ultraviolet and visible region (Uv-Vis). The infrared results indicated the coordination of the bidentate ligand kojic acid, due to reductions in the values of the stretching frequencies of the carbonyl and double bonds, compared to the free ligand for all complexes obtained. The presence of new vibrational modes indicated the change of symmetry of the molecules in the new compounds synthesized. Additionally, the presence of vibrational modes assigned to metal-oxygen also contributed to confirm the ligand coordinating to the metal ions. Through this technique, was also possible to perform correlations of the numbers of vibrational modes, in the region 1400-900 cm-1 and the compounds geometry. The heteroleptic compounds exhibited υC≡N in 2065 and 2053 cm-1, respectively, for the trans-K2[Fe(kj)2(CN)2] and trans-Na2[Ru(kj)2(CN)2], indicating coordination of the cyano ligand to metal ions FeII e RuII. Comparing the obtained values with literature data was possible to identify the complex isomerism as trans. In relation to the results of electronic spectroscopy, studies of pH variation of kojic acid provided information on the distribution of electron density in the molecule, showing characteristic spectral profile of kojic ion and its protonated form (Hkj, kojic acid), with two bands at 215 and 269 nm, or deprotonated (kj-), with bands at 226 and 315 nm. The electronic spectra obtained for all complexes in aqueous medium, in the ultraviolet region, exhibited variations of the energies assigned to kojic acid intraligand transitions while in the visible region, only transitions assigned to charge transfer of iron and ruthenium complex have been identified / Com o presente trabalho tem-se como objetivo contribuir com a qu?mica de coordena??o do ligante ?cido k?jico, com a s?ntese e caracteriza??o de compostos homol?pticos [Al(kj)3], [Fe(kj)3], [Fe(kj)2], [Cu(kj)2] e [Ru(kj)3], assim como dos novos complexos heterol?pticos, trans-K2[Fe(kj)2(CN)2] e trans-Na2[Ru(kj)2(CN)2]. Os compostos obtidos foram caracterizados atrav?s da espectroscopia vibracional na regi?o do infravermelho e da espectroscopia eletr?nica na regi?o do ultravioleta e vis?vel (Uv-Vis). Os resultados de infravermelho comprovaram a coordena??o do ligante bidentado ?cido k?jico, devido ?s redu??es dos valores das frequ?ncias de estiramento da carbonila e das duplas liga??es, comparativamente ao ligante livre, para todos os complexos obtidos. Assim como a verifica??o de novos modos vibracionais, em decorr?ncia da altera??o de simetria da mol?cula na forma??o de novas estruturas para os compostos sintetizados. Al?m de modos vibracionais atribu?dos aos estiramentos metal-oxig?nio, evidenciando coordena??o dos ?ons met?licos ao ligante. Atrav?s dessa t?cnica, tamb?m foi poss?vel realizar correla??es dos n?meros de modos vibracionais, na regi?o de 1400 a 900 cm-1, com a geometria dos compostos. Adicionalmente aos complexos homol?pticos, os compostos heterol?pticos exibiram frequ?ncias de υC≡N em 2065 e 2053 cm-1, respectivamente, para o trans-K2[Fe(kj)2(CN)2] e o trans-Na2[Ru(kj)2(CN)2], indicando coordena??o do ligante ciano aos ?ons met?licos de FeII e RuII. Comparativamente com dados da literatura, foi poss?vel propor a isomeria, caracterizando os complexos em configura??o trans. E com rela??o aos resultados da espectroscopia eletr?nica, os estudos da varia??o do pH do ?cido k?jico forneceram informa??es sobre a distribui??o de densidade eletr?nica na mol?cula, apresentando perfil espectral caracter?stico do ?on k?jico na sua forma protonada (Hkj, ?cido k?jico), com duas bandas em 215 e 269 nm, ou desprotonada (kj-), com bandas em 226 e 315 nm. E os espectros eletr?nicos obtidos para todos os complexos em meio aquoso, na regi?o do ultravioleta exibiram varia??es das energias atribu?das ?s transi??es intraligantes do ?cido k?jico, e na regi?o do vis?vel, s? foram identificadas transi??es para os complexos de ferro e rut?nio, atribu?das em sua maioria as transfer?ncia de carga

Cette thèse présente divers aspects du polissage des eaux usées de galvanoplastie par des zones humides artificielles : analyse de la performance, étude de la configuration et de la mise en œuvre, influence de différentes sources de carbone, évolution du substrat, l'analyse des plantes et des problèmes de conception.Les objectifs de ce travail sont triples: (i) étudier la faisabilité du polissage des effluents de la galvanoplastie, (ii) étudier l'influence des systèmes opérationnels, des plantes, du substrat et de la charge des eaux usées, (iii) comprendre les mécanismes conduisant à une diminution de la charge métallique dans des microcosmes de zones humides construites.Ce travail a fourni de nouvelles informations et élargi les connaissances actuelles sur le traitement des eaux usées industrielles dans les zones humides artificielles. En fait, il s'agit, à notre connaissance, de la première étude concernant l'élimination des métaux et du cyanure d'eaux usées par des zones humides artificielles en écoulement de sub-surface. / This thesis presents various aspects of polishing the electroplating wastewater in constructed wetlands: analysis of the performance, study on the operation and configuration effects, effects of various carbon sources, analysis of the substrate (bed media), analysis of plants, and design issues.The goals of the experiment were to: (i) study the feasibility of polishing electroplating effluent, (ii) study the effect of operating schemes, plants, bed media and wastewater strength, (iii) to elucidate metal removal mechanisms in the CW microcosms.This study furnished new information and expanded the existing knowledge on industrial wastewater treatment in constructed wetlands. In fact, this is, to the best knowledge, the first publication studying the removal of metals and cyanide from electroplating wastewater in subsurface flow constructed wetlands. The aim of this study was to study the polishing of the electroplating wastewater pretreated using physical-chemical methods.

This thesis presents various aspects of polishing the electroplating wastewater in constructed wetlands: analysis of the performance, study on the operation and configuration effects, effects of various carbon sources, analysis of the substrate (bed media), analysis of plants, and design issues.The goals of the experiment were to: (i) study the feasibility of polishing electroplating effluent, (ii) study the effect of operating schemes, plants, bed media and wastewater strength, (iii) to elucidate metal removal mechanisms in the CW microcosms.This study furnished new information and expanded the existing knowledge on industrial wastewater treatment in constructed wetlands. In fact, this is, to the best knowledge, the first publication studying the removal of metals and cyanide from electroplating wastewater in subsurface flow constructed wetlands. The aim of this study was to study the polishing of the electroplating wastewater pretreated using physical-chemical methods.

Aphrodisiac and anti-aphrodisiac pheromone production and composition in the green-veined white butterfly Pieris napi L. were investigated. Aphrodisiac pheromone biosynthesis had different time constraints in butterflies from the diapausing and directly developing generations. Effects of stable isotope incorporation in adult butterfly pheromone, in the nectar and flower volatiles of  host plants from labeled substrates were measured by solid phase microextraction and gas chromatography–mass spectrometry. A method to fertilize plants with stable isotopes was developed and found to be an effective method to investigate the transfer of pheromone building blocks from flowering plants to butterflies. The anti-aphrodisiac methyl salicylate was not biosynthesized from phenylalanine in flowers of Alliaria petiolata. Both aphrodisiac and anti-aphrodisiac pheromones in P.napi are produced not only from resources acquired in the larval stage, but also from nutritional resources consumed intheadult stage. Males of P. napi produce the anti-aphrodisiac pheromone from both the essential amino acid L-phenylalanine and from common flower fragrance constituents. / <p>QC 20140311</p>