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Relevant bibliographies by topics / Electrochemistry, Industrial

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Academic literature on the topic 'Electrochemistry, Industrial'

Author: Grafiati

Published: 4 June 2021

Last updated: 31 July 2024

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Journal articles on the topic "Electrochemistry, Industrial"

1

Scott, K. "Industrial Electrochemistry." Electrochimica Acta 36, no. 14 (January 1991): 2193. http://dx.doi.org/10.1016/0013-4686(91)85229-z.

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Parsons, Roger. "Industrial Electrochemistry." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 187, no. 1 (May 1985): 203. http://dx.doi.org/10.1016/0368-1874(85)85587-8.

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Barendrecht, E. "Industrial electrochemistry." Applied Surface Science 45, no. 1 (August 1990): 91–92. http://dx.doi.org/10.1016/0169-4332(90)90025-u.

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McIntyre, James. "100 Years of Industrial Electrochemistry." Journal of The Electrochemical Society 149, no. 10 (2002): S79. http://dx.doi.org/10.1149/1.1508412.

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Kenis, Paul, and Maria Inman. "Panel - the IE&EE Division at 80." ECS Meeting Abstracts MA2023-01, no. 24 (August 28, 2023): 1612. http://dx.doi.org/10.1149/ma2023-01241612mtgabs.

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The Industrial Electrochemistry and Electrochemical Engineering (IE&EE) division was established in 1943. This session will feature a panel discussion where experts in the field will share their thoughts on the evolution of in industrial electrochemistry and electrochemical engineering over the years, as well as current trends and future opportunities in these fields. Confirmed panelists will be announced in this abstract before the meeting.

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Sone, Masato. "Electrochem: An International Scientific Open Access Journal to Publish All Faces of Electrochemistry, Electrodeposition, Electrochemical Analysis, Electrochemical Sensing and Other Aspects about Electrochemical Reaction." Electrochem 1, no. 1 (February 25, 2020): 1–3. http://dx.doi.org/10.3390/electrochem1010001.

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Our aim of journal Electrochem is to provide reviews, regular research papers, and communications in all areas of electrochemistry including methodologies, techniques, and instrumentation in both fundamental and applied fields. In this Editorial, the various technological demands for electrochemistry from academic and industrial fields are discussed and some problems to be solved in electrochemistry are proposed for next-generation science and technology. Under these technological demands, open access journals such as Electrochem will provide the solutions and new technology in electrochemistry to the world.

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Inman, Maria. "The Future of Industrial Electrochemistry & Electrochemical Engineering." Electrochemical Society Interface 32, no. 2 (June 1, 2023): 39–40. http://dx.doi.org/10.1149/2.f07232if.

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Since its inception, the work of the Industrial Electrochemistry & Electrochemical Engineering (IE&EE) Division has encompassed a broad range of technologies and applications, including mathematical modeling of electrochemical systems, development and optimization of small- and large-scale industrial processes, environmental remediation and electrochemical conversion to produce value-added chemicals. A recent focus has been the creation of innovative technologies that will help to alleviate the climate and environmental crises, to improve sustainability and decarbonize existing technologies.

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Stenner, P. "Novel industrial applications for electrochemistry – Expecting the unexpected." Chemie Ingenieur Technik 92, no. 9 (August 28, 2020): 1159–60. http://dx.doi.org/10.1002/cite.202055278.

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Schievano, Andrea, Tommy Pepé Sciarria, Karolien Vanbroekhoven, Heleen De Wever, Sebastià Puig, Stephen J. Andersen, Korneel Rabaey, and Deepak Pant. "Electro-Fermentation – Merging Electrochemistry with Fermentation in Industrial Applications." Trends in Biotechnology 34, no. 11 (November 2016): 866–78. http://dx.doi.org/10.1016/j.tibtech.2016.04.007.

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ITO, Yasuhiko, Tokujiro NISHIKIORI, and Hiroyuki TSUJIMURA. "Novel Molten Salt Electrochemical Processes for Industrial Applications." Electrochemistry 86, no. 2 (2018): 21–28. http://dx.doi.org/10.5796/electrochemistry.18-h0001.

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Dissertations / Theses on the topic "Electrochemistry, Industrial"

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Scott, Leonard Lindsay. "Electrolytic manufacture of thiosulfate-free solutions of sodium hydrosulfite from aqueous sodium bisulfite." Diss., Georgia Institute of Technology, 1997. http://hdl.handle.net/1853/10241.

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Brimecombe, Rory Dennis. "Nanomaterial modified electrodes : optimization of voltammetric sensors for pharmaceutical and industrial application." Thesis, Rhodes University, 2011. http://hdl.handle.net/10962/d1009721.

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Nanomaterials, in particular carbon nanotubes have been shown to exhibit favourable properties for the enhancement of electrochemical detection of target analytes in complex matrices. There is however scope for improvement in terms of the optimization thereof in electrochemical sensors surface modification. The aim of this thesis was to examine methods that would result in increased current response, lowered passivation and application of such modified surfaces with application to pharmaceutically and industrially relevant analytes. Current methods for enhancing the performance of carbon nanotubes include acid functionalization which not only increases the hydrophilicity of the nanotubes, and consequently their ability to provide stable (aqueous) suspensions, but also introduces electrochemically active sites. This particular approach is however not normalized in the literature. Over-exposure to acid treatment results in loss of structural integrity of the carbon nanotubes, and as such a fine balance exists between achieving these dual outcomes. Guided by high resolution scanning electron microscopy, atomic force microscopy, voltammetric and impedance studies, this thesis examined the role of the length of time of the acid functionalization process as well as the impact of activation of carbon nanotubes and fullerenes on electrochemical sensor performance. Based on desired charge transfer resistances, rate transfer coefficients and sensitivity towards redox probes the optimal length of acid functionalization for multiwalled carbon nanotubes was 9 hours and 4 hours for single-walled carbon nanotubes. Further improvements in the desired outcomes were achieved through electrochemical activation of the modified electrode surface by cycling in the presence of catechol, in a novel approach. By employing electrochemical impedance spectroscopy it was observed that catechol activation resulted in lowered charge transfer resistance, before and after activation, with functionalized multi-walled carbon nanotubes (9 hours) exhibiting the greatest decrease of 90 % and functionalized single-walled carbon nanotubes (4 hours), a 50 % decrease. Corresponding increases in the heterologous rate transfer coefficient showed a 770 % increase for functionalized multi-walled carbon nanotubes (9 hours), following catechol activation. Comparative observations for fullerenes following partial reduction in potassium hydroxide yielded a 30 % decrease in charge transfer resistance, with an increased heterologous rate transfer coefficient at a fullerene modified surface The performance of the nanomaterial modified electrodes was applied to the detection of wortmannin with applications in bioprocess control and in the pharmaceutical sector as well as to the detection and monitoring of the industrial dye Reactive red. Of particular relevance to these analytes was the assessment of the nanomaterial modified electrodes for enhanced stability, reproducibility, sensitivity and decreased passivation effects. In this study the first known account of wortmannin detection through electrochemical methods is reported. Voltammetric characterization of wortmannin revealed an irreversible cathodic process with a total number of 4 electrons and a diffusion coefficient of 1.19 x 10-7 cm².s⁻¹. At a functionalized multiwalled carbon nanotubes modified glassy carbon electrode a limit of detection of 0.128 nmol.cm⁻³ was obtained, and with limited surface passivation the detection scheme afforded pertinent analyses in biological media representing a substantial improvement over chromatographic detection methods. This study also provided the first account of the voltammetric detection of reactive red, competing favourably with traditional spectroscopic methods for monitoring biodegradation of this compound in real time.

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Naidoo, Kaveshini. "Electrochemical behavious of boron-doped diamond electrodes." Pretoria : [s.n.], 2001. http://upetd.up.ac.za/thesis/available/etd-11212005-173041/.

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Tau, Prudence Lerato. "Study of titanium, tantalum and chromium catalysts for use in industrial transformations." Thesis, Rhodes University, 2007. http://hdl.handle.net/10962/d1005028.

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PART A The syntheses, spectroscopic and electrochemical characterisation of a series of titanium and tantalum phthalocyanine complexes are reported. The complexes are unsubstituted and substituted at either the peripheral or non-peripheral positions with sulphonates, aryloxy, arylthio or amino groups. The complexes mostly exhibit Qbands in the near-infrared region as well as interesting properties in different solvents. The interaction of differently sulphonated titanium and tantalum phthalocyanine complexes with methyl viologen (MV[superscript 2+]), and hence the stoichiometry and association constants are evaluated. Detailed photophysicochemical properties of the complexes were investigated and are for the first time presented with fluorescence lifetimes easily obtained from fluorescence quenching studies. The transformation of 1-hexene photocatalysed by aryloxy- and arylthio-appended complexes is also presented for the first time. The electrochemical properties of the complexes are unknown and are thus presented. Cyclic (CV) and square wave (SWV) voltammetries, chronocoulometry and spectroelectrochemistry are employed in the study of the complexes. Two oneelectron reductions and a simultaneous 4-electron reduction are observed for the unsubstituted Cl[subscript 3]TaPc. Reduction occurs first at the metal followed by ring-based processes. The tetra- and octa-substituted derivatives however exhibit peculiar electrochemical behaviour where a multi-electron transfer process occurs for complexes bearing certain substituents. For all complexes, the first two reductions are metal-based followed by ring-based processes. A comparative study of the electrocatalytic activities of the complexes towards the oxidation of nitrite is also investigated. The complexes are immobilised onto a glassy carbon electrode either by drop-dry or electropolymerisation methods. All the modified electrodes exhibit improved electrocatalytic oxidation of nitrite than the unmodified electrodes by a twoelectron mechanism producing nitrate ions. Catalytic currents are enhanced and nitrite overpotential reduced to ~ 0.60 V. Kinetic parameters are determined for all complexes and a mechanism is proposed. PART B: The syntheses and electrochemical characterisation of chromium and titanium complexes for the selective trimerisation of ethylene to 1-hexene are presented. The synthesis of the chromium complex requires simple steps while tedious steps are used for the air-sensitive titanium complex. The spectroscopic interaction of the chromium complex with the co-catalyst methylaluminoxane is investigated. The complexes are characterised by electrochemical methods such as cyclic voltammetry and spectroelectrochemistry.

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Parikh, Harshil R. "Modeling and analysis of proton exchange membrane fuel cell." Ohio : Ohio University, 2004. http://www.ohiolink.edu/etd/view.cgi?ohiou1088438486.

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Pereira, Wellington da Silva. "Estudo da aplicação de ferro zero no tratamento de efluente têxtil." Universidade de São Paulo, 2004. http://www.teses.usp.br/teses/disponiveis/46/46132/tde-05092016-144057/.

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O presente trabalho de mestrado descreve o estudo da viabilidade da aplicação de ferro de valência zero no tratamento de quatro classes de corantes muito utilizados pela indústria têxtil: corante preto remazol B (azo), vermelho remazol RB 133 (triazina), azul remazol brilhante RN (antraquinona) e turquesa remazol G 133 (ftalocianina). O processo também foi aplicado na remediação de um efluente têxtil. O Fe0 mostrou uma grande eficiência na degradação dos corantes estudados, empregando-se uma concentração de Fe0 de 5 g L-1 (oriundo de um resíduo de processo metalúrgico) no tratamento de soluções de azocorantes com concentração de 100 mg L-1, obteve-se uma taxa de descoloração superior a 90% em apenas 15 minutos de tratamento. Uma característica bastante favorável do processo proposto foi sua ampla faixa operacional de pH, observando-se uma degradação do grupo cromóforo superior a 80% para soluções com pH entre 1,5 e 9 (sendo a faixa ótima observada entre 3 e 5). O processo também se mostrou pouco susceptível a variações na concentração de corante (faixa estudada: 25 - 150 mg L-1). Por outro lado, a eficiência do tratamento com ferro de valência zero mostrou-se dependente do tamanho de partícula, da massa e da superfície do material metálico. O mecanismo de degradação também variou em função do emprego de condições anaeróbias ou aeróbias. Para 15 minutos de tratamento, a descoloração dos corantes e do efluente têxtil atingiu níveis ao redor de 95% independente da condição anaeróbia/aeróbia. Entretanto na presença de O2 , observou-se uma redução do carbono orgânico total de até 75% (contra cerca de 25% na condição anaeróbia), mostrando que quando esta espécie aceptora de elétrons esta presente, o mecanismo envolve etapas de oxidação, provavelmente associadas a reações do tipo Fenton. O processo de tratamento emp~egando Fe0 apresentou uma cinética de pseudo-primeira ordem para a degradação dos grupos cromóforos e para a mineralização da matéria orgânica dos corantes e do efluente real. Para os corantes, as constantes cinéticas apresentaram a seguinte ordem: ftalocianina < azo < antraquinona < triazina. De um modo geral, o processo remediatiyo estudado apresentou boas características, que o capacitam como uma alternativa promissora para o tratamento de corantes e efluentes têxteis.
This work describes a study to evaluate the viability of zero-valent iron in the treatment of four classes of dyes that are commonly used in the textile industry: Remazol Black B (azo), Remazol Red RB133 (triazine), Remazol Brilliant Blue RN (anthraquinone) and Remazol Turquoise G133 (phtalocyanine). The process was also apllied in the textile effluent remediation. Fe0 process showed a great efficiency in the degradation of the studied dyes, it was obtained a discoloration level higher than 90% in just 15 minutes of treatment employing 5 g L-1 of Fe0 (obtained from of a metallurgic residue) in the degradation of 100 mg L-1 azodye solutions. A quite favorable characteristic of the proposed process was the wide pH operational range; the degradation of chromophore group was upper to 80% for azodye solutions with pH between 1,5 and 9 (the optimum range observed between 3 and 5). The process showed low susceptibility to variations in dye concentration (studied range: 25 - 150 mg L-1). On the other hand, the efficiency of the treatment with zero-iron valence zero was dependent on particle size, mass and surface of the metallic material. The degradation mechanism also varied as function of anaerobic and aerobic conditions. For 15 minutes of treatment, the discoloration of studied dyes and textile effluent reached levels around 95% independent of anaerobic/aerobic condition. However, in the presence of O2, the total arganic carbon showed a reduction up to 75% (versus just around 25% observed in the anaerobic condition). These results showed that when this electron acceptor species is present, the mechanism involves oxidation stages, probably associated with type Fenton reactions. The treatment using Feo presented pseudo-first arder kinetics for the degradation of chromophore groups and for organic matter mineralization. The kinetic constants presented the following order for the studied dyes: phtalocyanine < azo < anthraquinone < triazine. In general, the studied remediative process showed some good characteristics, which makes it a promising alternative for the treatment of dyes and textile effluents.

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Khatib, Maher Al. "EPR Spectroscopy for the investigation of materials of technological and industrial interest." Doctoral thesis, Università di Siena, 2019. http://hdl.handle.net/11365/1070360.

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The research presented in this Doctoral Thesis discusses mainly the use of Electron Paramagnetic Spectroscopy for the characterization of materials of technological interest. The longitudinal relaxation properties of a vanadyl porphyrin complex have been investigated using pulse EPR experiments at Q (34 GHz) and J-band (263 GHz) frequencies, and the molecule proposed as suitable candidate for quantum processors engineering. The experimental knowledge developed through these relaxation studies, have been transferred to the field of melanins biopigments characterization. The interest for this class of biopigments was derived from the vast amount of applications melanin can cover in the electrochemical and optoelectronic field (e.g. low immunoresponse coating for medical electroanalytical devices, or UV-Vis radiation absorber for solar energy harvesting devices). A novel bacterial melanin from Streptomyces cyaneofuscatus bacteria, and melanin pigments of enzymatic origin, were first studied through S (4 GHz), X (9 GHz) and Q-band (34 GHz) multifrequency EPR. The composition of the bacterial and enzymatic pigments was described, with the support of computer simulation and existing literature in the field. The relaxation properties of these melanin pigments were investigated by means of X and Q-band continuous wave EPR, as well as with Q-band pulse EPR experiments. Differences in terms of longitudinal relaxation times were observed for the melanin pigments of different origin, so that pulse EPR could be proposed either as a tool to distinguish among different melanin species, as well as probe to investigate the structure and dynamics of the radical species present in these natural pigments. A last chapter on the use of computer simulations for the modeling of the electrochemical devices that could be designed to host melanin coated electrodes is presented. In that context, a general model for the evaluation of electrodic currents generated under different geometrical and physical parameters of the systems has been proposed. The physical description was carried out using a dimensionless form of the governing equations, so that the findings of that research can be adapted to particular cases of study. The diverse content of the thesis is thought to reflect the multidisciplinary nature of materials research.

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Stevens, Michaela. "Fundamentals and Industrial Applications: Understanding First Row Transition Metal (Oxy)Hydroxides as Oxygen Evolution Reaction Catalysts." Thesis, University of Oregon, 2017. http://hdl.handle.net/1794/22633.

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Intermittent renewable energy sources, such as solar and wind, will only be viable if the electrical energy can be stored efficiently. It is possible to store electrical energy cleanly by splitting the water into oxygen (a clean byproduct) and hydrogen (an energy dense fuel) via water electrolysis. The efficiency of hydrogen production is limited, in part, by the high kinetic overpotential of the oxygen evolution reaction (OER). OER catalysts have been extensively studied for the last several decades. However, no new highly active catalyst has been developed in decades. One reason that breakthroughs in this research are limited is because there have been many conflicting activity trends. Without a clear understanding of intrinsic catalyst activity it is difficult to identify what makes catalysts active and design accordingly. To find commercially viable catalysts it is imperative that electrochemical activity studies consider and define the catalyst’s morphology, loading, conductivity, composition, and structure. The research goal of this dissertation is twofold and encompasses 1) fundamentally understanding how catalysis is occurring and 2) designing and developing a highly active, abundant, and stable OER catalyst to increase the efficiency of the OER. Specifically, this dissertation focuses on developing methods to compare catalyst materials (Chapter II), understanding the structure-compositional relationships that make Co-Fe (oxy)hydroxide materials active (Chapter III), re-defining activity trends of first row transition metal (oxy)hydroxide materials (Chapter IV), and studying the role of local geometric structure on active sites in Ni-Fe (oxy)hydroxides (Chapter V). As part of a collaboration with Proton OnSite, the catalysts studied are to be integrated into an anion exchange membrane water electrolyzer in the future. This dissertation includes previously published and unpublished co-authored material.
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Woodcock, Christopher Paul. "A review and development of accelerated test methods for anti-corrosive organic coatings." Thesis, University of Northampton, 2007. http://nectar.northampton.ac.uk/2665/.

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To enable improvements in the development of anti-corrosive coatings quick methods of evaluation are required and several are available which are both qualitative and quantitative. This investigation reviews both types of method, the first in the form of traditional salt spray exposure and the second in the form of electrochemical techniques. The emphasis in the experimental work reported here is on the Electrochemical Noise Measurement (ENM). ENM has been used to monitor coatings under immersion conditions, the aim being to assist a paint company develop a set of more environmentally friendly coatings. The immersion test has also incorporated a temperature cycle which proved effective at separating ‘good’ coatings within a short timeframe. Results showed good correlation between ENM and salt spray testing. Work is also reported which was done with the aim of making the ENM method more practically useful. The standard configuration (‘Bridge’) requires two separate specimens which is unattractive for site work. The Single Substrate (SS) arrangement was developed to get around this problem but this still requires the metal to be connected to the measuring instrument. This is avoided in the most recent development which needs No Connection to Substrate (NOCS). Results are given for immersed samples monitored using the ENM NOCS arrangement and compared with the standard ‘Bridge’ method and DC resistance. Results are also presented using sets of different electrodes (platinum, calomel and silver/silver chloride). This preliminary work has shown that the NOCS method holds great promise. In the laboratory Electrochemical Impedance Spectroscopy (EIS) is also commonly employed to assess the performance of anti-corrosive coatings. Concluding this work a comparison of the ENM and EIS techniques was undertaken on a set of laboratory samples. Results showed that both methods had the ability to rank the performance of coatings. However ENM’s advantages (as outlined above) were confirmed

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Borin, Antonio Carlos. "Reator eletroqu¡mico de bancada para remoção de íons de metais a partir de efluentes industriais." Universidade de São Paulo, 1986. http://www.teses.usp.br/teses/disponiveis/46/46132/tde-04072012-083932/.

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Foi projetado e construído um reator eletroquímico de bancada com a finalidade de simular a purificação de efluente industrial contendo íon metálico. As condições levadas em conta no projeto e nos testes de avaliação do reator eram baseadas em dados operacionais reais da indústria. Assim, tratou-se soluções contendo 15.900 ppm de Cu2+ (0,25 M), uma concentração típica de efluentes de cobre, procurando-se chegar o mais perto possível do valor permitido pela CETESB, ou seja 1 ppm (15,7 µM). Foram empregados como eletrodos quatro placas de grafite comercial de 600 X 150 X 10 mm, uma bomba centrífuga de vazão igual a 0,3 L.s-1 para circulação do eletrólito, e fontes de corrente com saída de 0 a 20 A totais. Como foi constatado que os grafites encontráveis no mercado nacional apresentam comportamento bem diverso, realizou-se um estudo do desempenho de materiais de procedência diferentes, em escala de laboratório. Os eletrodos de grafite foram dispostos, guardando entre si um espaçamento de 5 mm, sobre placas de vidro, ligados, eletricamente, no sistema bipolar. Todas as paredes do reator foram feitas de vidro para que se pudesse observar o seu interior durante e após a operação. De cada vez foram tratados 10 litros de solução contendo o íon metálico, e acidulado na base de 10% em H2S04 (v/v), sendo que o eletrólito era reciclado na célula durante um tempo da ordem de 20 horas. Numa comparação das concentrações calculadas, para diversos tempos, e os dados experimentais reais revela certa discrepância. Tal discrepância parece aceitável nesse tipo de operação. Assim, as concentrações de cobre observadas são, quase sempre, superiores às calculadas. Entretanto, os dois valores convergem à medida que decorre o tempo de eletrólise. Por exemplo, após 15 horas de eletrólise, com uma corrente de operação igual a 20 A, deveria reduzir a concentração de 15.900 ppm para 7,2 ppm, quando o valor observado experimentalmente foi de 9 ppm. Obteve-se, assim, uma conversão de 99%, que como revelaram os estudos, parece ser o valor máximo atingível com o reator construido. Embora essa conversão seja considerada excelente, não parece viável atingir os valores da CETESB apenas numa única operação de eletrólise, e no futuro operações complementares deverão ser procuradas. O cobre recuperado apresenta um custo alto comparativamente com o preço de mercado, permanecendo, como principal vantagem do processo, o benefício ecológico.
An electrochemical reactor, with the aim of recovering metallic ions from waste water, was designed, built and evaluated in laboratory scale. The working conditions concerning to the ion concentrations were based in real operational data. Thus, solutions containing 15,900 ppm Cu2+ ions (0.25 M) were electrolysed with the purpose of obtain a final concentration as near as possible to the limiting value which is allowed by CETESB (Companhia de Tecnologia de Saneamento Ambiental), i.e., 1 ppm (15.7 µM). Four commercial graphite plates (600 X 150 X 10 mm), of different origins,were employed as electrodes. A centrifugal pump with capacity equal to 0.3 L.s-1 was used to circulate the electrolyte through the reactor. The electric current was supplied by sources with a maximum output of 20 A. The performance of the different graphite, which are available at the Brazilian market was studied further by means of potentiodynamic experiments, using electrodes with areas of few square millimeters. The reactor was built with glass to make possible visual observations of the inside. Two adjacent electrodes were separated by 5 mm. At each experiment 10 liters of solution containing the metallic ion and 10% H2S04 (v/v) were electrolysed for about 20 hours. The calculated values and the experimental ones, for different electrolysis times, show some deviation. This deviation, however, seems to be reasonable in that kind of experiments. Calculated and experimental values converge to the same limit with time. For example, after 15 hours electrolysis with an operating current of 20 A, the initial concentration, 15,900 ppm, is reduced to 9 ppm, when the calculated value is 7,2 ppm. Thus, a 99% conversion is attained. This is apparently, the limiting value which is attainable with the reactor. Although, this conversion value may be considered very good, it does not seems possible to obtain the limiting value, imposed by CETESS, with a one-step electrochemical operation. The cost of the recovered copper is high compared with the market price. Therefore, the main benefice of process is the ecological one.

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Books on the topic "Electrochemistry, Industrial"

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Pletcher, Derek, and Frank C. Walsh. Industrial Electrochemistry. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2154-5.

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Pletcher, Derek. Industrial electrochemistry. 2nd ed. London: Chapman and Hall, 1989.

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Pletcher, Derek. Industrial electrochemistry. 2nd ed. London: Chapman and Hall, 1990.

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1952-, Walsh Frank, ed. Industrial electrochemistry. 2nd ed. London: Blackie Academic & Professional, 1993.

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Singh, Vijay G. Applied electrochemistry. Hauppauge, N.Y: Nova Science Publishers, 2009.

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Singh, Vijay G. Applied electrochemistry. Hauppauge, N.Y: Nova Science Publishers, 2009.

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G, Willard Thomas, ed. Solid state electrochemistry. Hauppauge, N.Y: Nova Science Publishers, 2009.

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Hine, Fumio. Electrodeprocesses and electrochemical engineering. New York: Plenum Press, 1985.

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J, Mulky M., Srivastava H. C, Vatsya Bhartendu, and Menon K. K. G, eds. Industrial research. New Delhi: Oxford & IBH Pub. Co., 1988.

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Kalia, R. K. Impact of new electrochemical technologies and processes on the demand for electrical energy. Montréal, Qué: Canadian Electrical Association, 1986.

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Book chapters on the topic "Electrochemistry, Industrial"

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Hibbert, D. Brynn. "Industrial electrochemistry." In Introduction to electrochemistry, 274–93. London: Macmillan Education UK, 1993. http://dx.doi.org/10.1007/978-1-349-22721-1_12.

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Leddy, James J. "Industrial Electrochemistry." In ACS Symposium Series, 478–509. Washington, DC: American Chemical Society, 1989. http://dx.doi.org/10.1021/bk-1989-0390.ch033.

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Pletcher, Derek, and Frank C. Walsh. "Fundamental concepts." In Industrial Electrochemistry, 1–59. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2154-5_1.

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Pletcher, Derek, and Frank C. Walsh. "Corrosion and its control." In Industrial Electrochemistry, 481–542. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2154-5_10.

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Pletcher, Derek, and Frank C. Walsh. "Batteries and fuel cells." In Industrial Electrochemistry, 543–95. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2154-5_11.

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Pletcher, Derek, and Frank C. Walsh. "Electrochemical sensors and monitoring techniques." In Industrial Electrochemistry, 596–637. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2154-5_12.

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Pletcher, Derek, and Frank C. Walsh. "Electrochemical engineering." In Industrial Electrochemistry, 60–172. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2154-5_2.

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Pletcher, Derek, and Frank C. Walsh. "The chlor-alkali industry." In Industrial Electrochemistry, 173–209. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2154-5_3.

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Pletcher, Derek, and Frank C. Walsh. "The extraction, refining and production of metal." In Industrial Electrochemistry, 210–48. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2154-5_4.

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Pletcher, Derek, and Frank C. Walsh. "Other inorganic electrolytic processes." In Industrial Electrochemistry, 249–93. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2154-5_5.

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Conference papers on the topic "Electrochemistry, Industrial"

1

Rabernecker, Peter. "Electrochemical Sensors: trace detection for specific detection and pattern recognition for complex matrices." In 1st International Seminar on Industrial Innovation in Electrochemistry. São Paulo: Editora Edgard Blücher, 2014. http://dx.doi.org/10.5151/chempro-s3ie-04.

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Berton, Marcos Antonio Coelho, Luiz Carlos Ferracin, and Filipe Miguel Cassapo. "Strategies to Promote the Innovation in Brazilian Industry: The creation of SENAI Institute of Innovation." In 1st International Seminar on Industrial Innovation in Electrochemistry. São Paulo: Editora Edgard Blücher, 2014. http://dx.doi.org/10.5151/chempro-s3ie-01.

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D´Alkaine, Carlos V. "Corrosion: technical problems, professional resources, working organization and RDAndamp;I characteristics for the Brazilian Productive Sector." In 1st International Seminar on Industrial Innovation in Electrochemistry. São Paulo: Editora Edgard Blücher, 2014. http://dx.doi.org/10.5151/chempro-s3ie-02.

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Berton, M. A. C., Paulo R. D. Marangoni, and Nério Vicente Júnior. "Foreword." In 1st International Seminar on Industrial Innovation in Electrochemistry. São Paulo: Editora Edgard Blücher, 2014. http://dx.doi.org/10.5151/chempro-s3ie-00.

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Björk, Per, Roodabeh Afrasiabi, Nima Jokilaakso, Si Chen, Apurba Dev, Michel Salter, Shi-Li Zhang, Amelie Eriksson Karlström, and Jan Linnros. "Silicon nanowires/nanoribbons for label-free electrical detection of biomolecules." In 1st International Seminar on Industrial Innovation in Electrochemistry. São Paulo: Editora Edgard Blücher, 2014. http://dx.doi.org/10.5151/chempro-s3ie-03.

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Junqueira, Rosa Maria Rabelo, and Célia Regina de Oliveira Loureiro. "Electrochemical coloration of stainless steel as an alternative for architectural coatings." In 1st International Seminar on Industrial Innovation in Electrochemistry. São Paulo: Editora Edgard Blücher, 2014. http://dx.doi.org/10.5151/chempro-s3ie-05.

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Andrade, Márcio Henrique S., and Josealdo Tonholo. "Development of Technology in University-Industry Partnership: A Groundbreaking Case in the Northeast of Brazil." In 1st International Seminar on Industrial Innovation in Electrochemistry. São Paulo: Editora Edgard Blücher, 2014. http://dx.doi.org/10.5151/chempro-s3ie-06.

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Schiavinato, Luander A. A., Pedro N. G. Dias, Beatriz A. Pinto, Maria A. R. F. da Cruz, Ivani A. Carlos, Zulema A. Mahmud, João R. S. Moreno, and Paulo C. Tulio. "Self-lubricating metal-matrix composite CuZn-graphite coatings obtained by electrodeposition from near neutral solutions. Surface morphological analyses and chemical composition." In 1st International Seminar on Industrial Innovation in Electrochemistry. São Paulo: Editora Edgard Blücher, 2014. http://dx.doi.org/10.5151/chempro-s3ie-07.

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Santos, G. A., A. G. S. G. Silva, L. S. Sanches, H. A. Ponte, and C. E. B. Marino. "Electrochemical detection of hydrogen uptake in electrodeposited nickel/nickel hydroxide system to prevent corrosion process." In 1st International Seminar on Industrial Innovation in Electrochemistry. São Paulo: Editora Edgard Blücher, 2014. http://dx.doi.org/10.5151/chempro-s3ie-08.

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Berton, M. A. C., Paulo R. D. Marangoni, Nério Vicente Júnior, and Sandro Malinovski. "Cure Characteristics of Industrial Commercial Paint Using Diffusion Wave Spectroscopy and the Some Properties of Paint Film Determinated by Electrochemical Impedance Spectroscopy." In 1st International Seminar on Industrial Innovation in Electrochemistry. São Paulo: Editora Edgard Blücher, 2014. http://dx.doi.org/10.5151/chempro-s3ie-09.

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