Academic literature on the topic 'Iodometria'

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Journal articles on the topic "Iodometria"

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Andrade, João Carlos de. "Determinações iodométricas." Revista Chemkeys, no. 2 (September 17, 2018): 1–6. http://dx.doi.org/10.20396/chemkeys.v0i2.9623.

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Os métodos volumétricos que utilizam reações de oxidação e redução dependem dos potenciais das semi-reações envolvidas mas, além dos potenciais favoráveis, os agentes oxidantes e redutores devem ser estáveis em solução e a substância a ser determinada deve ser colocada sob um determinado estado da oxidação, definido e estável, antes da titulação ser iniciada A iodometria é um método volumétrico indireto, onde um excesso de íons iodeto são adicionados à uma solução contendo o agente oxidante, que reagirá produzindo uma quantidade equivalente de iodo que será titulado com uma solução padronizada de tiossulfato de sódio.
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Pavani, Natália Peres Gonçalves, Ana Lúcia Colombo, and Setsuko Sato. "Avaliação da eficácia da fita teste utilizada para determinar a concentração do ácido peracético." Enfermagem Brasil 8, no. 3 (June 20, 2009): 144–48. http://dx.doi.org/10.33233/eb.v8i3.4659.

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O ácido peracético é um desinfetante de alto nível e esterilizante para artigos termossensíveis. Mas o processo de esterilização e desinfecção com o ácido peracético é um método de difícil monitoração quanto a sua efetividade. O estudo desenvolvido foi do tipo descritivo de caráter quantitativo, tendo como objetivo avaliar a eficácia dos métodos de monitoração dos processos de desinfecção e esterilização com ácido peracético, avaliando, assim, o aspecto fidedigno dos resultados obtidos com os testes, garantindo a confiança do profissional enfermeiro sobre os processos e sua tranqüilidade em relação à segurança de seus pacientes. Foram utilizados 2 tipos de amostras do ácido peracético, coletadas em 3 períodos de tempo diferentes. Após a coleta foram realizados 2 tipos de testes: com a fita teste (recomendado pelo fabricante do ácido) e o teste laboratorial para quantificação da concentração de ácido peracético presente na amostra (iodometria). Em seguida, os resultados dos testes foram comparados. Concluiu-se que os resultados obtidos com os testes laboratoriais são mais fidedignos, pois se aproximam da concentração de ácido peracético indicada pelo fabricante da solução. Além disso, concluiu-se, também, que a solução mantém uma concentração satisfatória de ácido peracético por um período de tempo maior que trinta dias.
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H. Dulanlebit, Yeanchon, Nikmans Hattu, Ritti P. Sangadji, Risma Mahulette, Nataniel Kelmanutu, and Sandriliati Asari. "Performance of Caffeine Content Analysis in Robusta sp and Theobroma cacao L using Iodometry, UV-Vis Spectrophotometry and High Performance Liquid Chromatography." Journal of Pure and Applied Chemistry Research 9, no. 3 (December 31, 2020): 212–21. http://dx.doi.org/10.21776/ub.jpacr.2020.009.03.535.

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Caffeine is a xanthine alkaloid compound found in Robusta sp and Theobroma cacao L. The caffeine extract was obtained by evaporating CHCl3 using a rotary evaporator and determine its content using iodometry, UV-Vis spectrophotometry and High Performance Liquid Chromatography, then validated by measurement methods. The iodometric caffeine content in Theobroma cacao L is 900 mg/kg while UV-Vis spectrophotometry is 4,000 mg/kg, and for HPLC in Robusta sp is 19,475 mg/kg. The iodometry performance gives the linearity value, R2 of 0.9791. The precision values at 5.0 mg/L and 15.0 mg/L are 4.6% and 8.3%. Accuracy for 5.0; 10.0; and 15.0 mg/L are 106%, 100% and 94% respectively. The performance of UV-Vis spectrophotometry gives linearity value, R2 of 0.9948. The precision value at 1.0 mg/L and 6.0 mg/L gives the variance coefficient value of 4.2% and 1.2%, while the accuracy at 1.0 mg/L and 6.0 mg/L are 99% and 101%.
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Albuquerque, Natália Porfírio, Ana Cristina Silva Muniz, and André Luiz Fiquene Brito. "USO DA ARGILA CHOCOLATE COMO ALTERNATIVA NO TRATAMENTO DE EFLUENTES DE REFINARIAS DE PETRÓLEO." HOLOS 1 (July 18, 2017): 229. http://dx.doi.org/10.15628/holos.2017.5151.

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Contando com uma produção média de 2 milhões e 799 mil barris de óleo por dia (bpd), o Brasil conta com 15 refinarias petróleo. Contudo, as refinarias têm forte impacto poluidor. Utilizam-se aproximadamente 246 a 340 litros de água por barril de petróleo cru, que serão responsáveis por 0,4 a 1,6 vezes de águas residuais em relação ao volume de óleo processado. As águas residuais têm como característica a presença de gases odorantes, destacando-se, o sulfeto de hidrogênio (H2S). O H2S é considerado como principal substância geradora de odor, pois proporciona incomodo já em baixas concentrações (0,00047 ppm). Portanto, a presente pesquisa buscou avaliar o tratamento de efluentes de refinarias de petróleo com teor de H2S por aeração, com e sem a presença da argila, buscando comparar o desempenho da mesma como adsorvente. Para isso montou-se um sistema piloto composto por 6 reatores, e utilizou-se a argila Chocolate em três deles. A concentração de H2S foi determinada por um detector multigases e por iodometria. Usou-se o planejamento experimental fatorial 2x2, onde foram estudados dois fatores: presença/ausência de argila, e o método utilizado. Para comprovar a significância dos resultados, realizou-se a análise de variância (ANOVA), com nível de significância de 5%. Os resultados encontrados mostraram que há diferença significativa entre o tratamento com e sem argila, como também entre os métodos utilizados. Constatou-se que os melhores resultados encontrados foram os que utilizaram a argila como adsorvente. A partir disso, obteve-se uma resposta otimizada do teor de H2S, de 8,1667 ppm.
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T, Rajkumar, Sivasanker Reddy L, Sivasanker Reddy L, Rajeswari V, and Rajeswari V. "SYNTHESIS AND CHARACTERIZATION OF INDINAVIR-Cu COMPLEX." Asian Journal of Pharmaceutical and Clinical Research 10, no. 7 (July 1, 2017): 289. http://dx.doi.org/10.22159/ajpcr.2017.v10i7.15359.

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Objective: The main objective of the present work is to synthesize Cu (II) indinavir, complex.Methods: The indinavir complexes were discussed with the help of spectroscopic instrumental methods such as infrared, ultraviolet, nuclear magnetic resonance, and mass and titrimetry methods (iodometry and potentiometry). Drug and drug metal complex are screened against antimicrobial activity.Results: The spectral studies show that the metal is coordinated to the drug in a bidentate manner. The titrimetry method, i.e., iodometric titration shows that metal bind to the drug in proportion of 1:1. The potentiometric titration curves of indinavir-Cu metal complex are mostly same which proves that the metal which might be present in the complex do not affect the titration curves. The result shows that the drug metal complex has enhanced inhibitory activity than drug under identical conditions in concentration ranges of 12.5 μg/ml in Staph and Bacillus species whereas in disc diffusion procedure zone of inhibition is 13 mm and 18 mm in Staph and Bacillus species.Conclusion: Indinavir-Cu complex had been synthesized and characterized by spectral techniques which shows enhanced microbial activity than drug.
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Bodiroga, Milanka, and Jasminka Ognjanovic. "Determination of peracetic acid and hydrogen peroxide in the mixture." Vojnosanitetski pregled 59, no. 3 (2002): 277–79. http://dx.doi.org/10.2298/vsp0203277b.

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Iodometric and permanganometric titrations were used for determination of peracetic acid and hydrogen peroxide (H2O2) in the mixture. Two procedures were described and compared. Titrations could be done in only one vessel, in the same reaction mixture, when iodometric titration of peracetic acid was continued after the permanganometric titration of H2O2, (procedure A). Peracetic acid and H2O2, as oxidizing agents, reacted with potassium iodide in an acid medium, evolving iodine. This reaction was used for the quantitative iodometric determination of total peroxide in procedure B. H2O2 reacted with potassium permanganate in acid medium, but peracetic acid did not react under the same conditions. That made possible the selective permanganometric determination of H2O2 in the presence of peracetic acid. The procedure B was performed in two titration vessels (KV=3.4% for peracetic acid, 0.6% for H2O2). The procedure A for iodometric determination of peracetic acid in one titration vessel after permanganometric titration of H2O2 was recommended (KV=2,5% for peracetic acid, 0,45% for H2O2).
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Meyiwa, Benson. "Iodometric and Iodimetric Titration Methods." Journal Wetenskap Health 1, no. 1 (September 30, 2020): 5–8. http://dx.doi.org/10.48173/jwh.v1i1.9.

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The discussion of this paper is to knowing and understanding the standard solution using the idometric and iodimetric titration methods. Experiment intent is to knowing and understanding the standard solution using the idometric and iodimetric titration methods. Therefore, the experiment purpose is to determine the levels of vitamin C based on the oxidation-reduction reaction using the iodimetric method, to determine the levels of CuSO4 based on oxidation-reduction reactions using the iodometric method and understanding the standard solution using the idometric and iodimetric titration methods.
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Hasanah, Uswatun. "PENENTUAN KADAR VITAMIN C PADA MANGGA KWENI DENGAN MENGGUNAKAN METODE IODOMETRI." JURNAL KELUARGA SEHAT SEJAHTERA 16, no. 31 (June 20, 2018): 90–95. http://dx.doi.org/10.24114/jkss.v16i31.10176.

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Khuthier, Abdul-Hussain, Abdul K. S. Al-Kazzaz, and Darwish Amin. "Iodometric determination of aryldialkylamine-N-oxides." Mikrochimica Acta 92, no. 4-6 (July 1987): 249–52. http://dx.doi.org/10.1007/bf01201847.

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Mertes, P., L. Pfaffenberger, J. Dommen, M. Kalberer, and U. Baltensperger. "Development of a sensitive long path absorption photometer to quantify peroxides in aerosol particles (Peroxide-LOPAP)." Atmospheric Measurement Techniques 5, no. 10 (October 2, 2012): 2339–48. http://dx.doi.org/10.5194/amt-5-2339-2012.

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Abstract. A new off-line instrument to quantify peroxides in aerosol particles using iodometry in long path absorption spectroscopy has been developed and is called peroxide long path absorption photometer (Peroxide-LOPAP). The new analytical setup features important technical innovations compared to hitherto published iodometric peroxide measurements. Firstly, the extraction, chemical conversion and measurement of the aerosol samples are performed in a closed oxygen-free (~ 1 ppb) environment. Secondly, a 50-cm optical detection cell is used for an increased photometric sensitivity. The limit of detection was 0.1 μM peroxide in solution or 0.25 nmol m−3 with respect to an aerosol sample volume of 1 m3. The test reaction was done at a constant elevated temperature of 40 °C and the reaction time was 60 min. Calibration experiments showed that the test reaction with all reactive peroxides, i.e. hydrogen peroxide (H2O2), peracids and peroxides with vicinal carbonyl groups (e.g. lauroyl peroxide) goes to completion and their sensitivity (slope of calibration curve) varies by only ±5%. However, very inert peroxides have a lower sensitivity. For example, tert-butyl hydroperoxide shows only 37% sensitivity compared to H2O2 after 1 h. A kinetic study revealed that even after 5 h only 85% of this inert compound had reacted. The time trends of the peroxide content in secondary organic aerosol (SOA) from the ozonolysis and photo-oxidation of α-pinene in smog chamber experiments were measured. The highest mass fraction of peroxides with 34% (assuming a molecular weight of 300 g mol−1) was found in freshly generated SOA from α-pinene ozonolysis. Mass fractions decreased with increasing NO levels in the photo-oxidation experiments. A decrease of the peroxide content was also observed with aging of the aerosol, indicating a decomposition of peroxides in the particles.
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Dissertations / Theses on the topic "Iodometria"

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Ly, Becky. "Jämförelse av metoder för peroxidbestämningar i bränslen : A comparison of methods for determination of peroxide content in fuel." Thesis, Linköping University, Department of Physics, Chemistry and Biology, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-58103.

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New energy resources that can replace petroleum diesel are needed and biodiesel may be an excellent substitute. During storage and use, biodiesel can oxidize and form peroxides, leading to degradation of the fuel. It is therefore important to determine the peroxide content of the fuel. In this thesis the triphenylphosphine method, which involves GC-MS analysis has been compared to the standard iodometric method which involves titration with sodium thiosulfate. Working standards were made to see how well the iodometric method worked and also in order to make a calibration curve in GC-MS. Aged samples were then analyzed. The results showed that both methods gave good linearity and repeatability with limits of detection (LOD) and quantification (LOQ) of 0,06 mM and 0 17-0,65 mM respectively. However, the iodometric method seemed more circumstantial since it needed a lot of solvents and different reagents. The triphenylphosphine method was on contrary very simple to use and did not require too much preparation work. The latter also showed better reproducibility. In conclusions, both methods can be used in evaluating the peroxide content of biodiesel, but the triphenylphosphine method has the advantages of higher simplicity and better reproducibility.

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Tozo, Greici Cristiani Gomes [UNESP]. "Análise qualitativa e quantitativa de cefoxitina sódica em injetáveis: desenvolvimento e validação de métodos analíticos e estudo de estabilidade." Universidade Estadual Paulista (UNESP), 2007. http://hdl.handle.net/11449/101326.

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Made available in DSpace on 2014-06-11T19:31:24Z (GMT). No. of bitstreams: 0 Previous issue date: 2007-10-30Bitstream added on 2014-06-13T19:20:21Z : No. of bitstreams: 1 tozo_gcg_dr_arafcf.pdf: 1418802 bytes, checksum: 299e470daf39de736e522b2d987e1a61 (MD5)
Universidade Estadual Paulista (UNESP)
A cefoxitina sódica (CAS 33564-30-6), antimicrobiano cefalosporínico, apresenta espectro de atividade contra microrganismos Gram-negativos mais amplo que as cefalosporinas mais antigas. Também é eficaz contra Proteus e Serratia indol-positivos, mostrando alta resistência à hidrólise por b-lactamases. Indicada no tratamento de peritonites e outras infecções intra-abdominais e intrapélvicas; sinusites, infecções ginecológicas, septicemias; endocardites; infecções do trato urinário, gonorréia não complicada, infecções do trato respiratório, ossos, articulações e pele. Apesar de este fármaco ser altamente estudado e pesquisado no que concerne à atividade antimicrobiana, farmacocinética e farmacodinâmica, há poucos estudos na literatura em relação ao desenvolvimento de metodologia analítica para esta cefalosporina. Desta forma, pesquisas envolvendo métodos analíticos são de fundamental importância e altamente relevantes para otimizar sua análise na indústria farmacêutica e farmpacia magistral de modo a garantir a qualidade do produto já comercializado. A proposta deste projeto foi desenvolver metodologias de análise para a cefoxitina sódica, fármaco comercializado no mercado médico-farmacêutico brasileiro. Foram desenvolvidos e validados métodos por CLAE com detector UV a 235 nm, com acetonitrila: água: ácido acético 5 M (22 : 78 : 1) como fase móvel e faixa de concentração de 20,0 à 30,0 μg/mL, tempo de retenção de 7,5 minutos. O coeficiente de correlação obtido foi de 0,9995 e a equação da reta y = 335,67x + 2391,9. O teste recuperação média obtido foi de 100,50%, com desvio padrão de 1,70%. O teor médio...
Sodium cefatoxin (CAS 33564-30-6), a cephalosporinic antibiotic, has a wider spectrum of activity against Gram-negative microrganisms than older cephalosporin. It is also efficient against the indol-positive Proteus and Serratia and has a high resistance to b- lactamases hydrolysis. Sodium cefatoxin is recommended for the treatment of peritonitis and other intra-abdominal and intra-pelvic infections; sinusitis, gynecological infections, septicemy, endocarditis; urinary tract infections, non-complicated gonorrhea, respiratory tract infections, bones, articulations and skin. Although this drug has been strongly studied and many researches have been developed about its antibiotics activity, pharmacokinetics and pharmacodynamics, there are few studies in the literature about the development of analytical methodology to this cephalosporin. Researches dealing with analytical methods are extremely important and highly relevant to optimize its analysis at the pharmaceutical industry and manipulation pharmacy, guaranteeing quality of the commercialized product. This project proposes the development of methodologies for analysis of sodium cefatoxin, a commercialized drug at the medical-pharmaceutical Brazilian market. Methods for CLAE with UV detector at 235nm were developed and validated with acetonitrile: water: acetic acid 5M (22: 78:1) as mobile phase and concentration range of 20.0 to 30.0 μg/mL, detention time of 7.5 minutes. The correlation coefficient obtained was 0.9995 and the line equation y = 335.67x + 2391.9. The medium recovery test was 100.50% with standard deviation of 1.70%. The medium content of sodium cefoxitin determined by CLAE... (Complete abstract click electronic access below)
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Tozo, Greici Cristiani Gomes. "Análise qualitativa e quantitativa de cefoxitina sódica em injetáveis : desenvolvimento e validação de métodos analíticos e estudo de estabilidade /." Araraquara : [s.n.], 2007. http://hdl.handle.net/11449/101326.

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Orientador: Hérida Regina Nunes Salgado
Banca: Marcos Antonio Segatto
Banca: Cristiane Masetto de Gaitani
Banca: Maria Virgínia Costa Scarpa
Banca: Thereza Christina Vessoni Penna
Resumo: A cefoxitina sódica (CAS 33564-30-6), antimicrobiano cefalosporínico, apresenta espectro de atividade contra microrganismos Gram-negativos mais amplo que as cefalosporinas mais antigas. Também é eficaz contra Proteus e Serratia indol-positivos, mostrando alta resistência à hidrólise por b-lactamases. Indicada no tratamento de peritonites e outras infecções intra-abdominais e intrapélvicas; sinusites, infecções ginecológicas, septicemias; endocardites; infecções do trato urinário, gonorréia não complicada, infecções do trato respiratório, ossos, articulações e pele. Apesar de este fármaco ser altamente estudado e pesquisado no que concerne à atividade antimicrobiana, farmacocinética e farmacodinâmica, há poucos estudos na literatura em relação ao desenvolvimento de metodologia analítica para esta cefalosporina. Desta forma, pesquisas envolvendo métodos analíticos são de fundamental importância e altamente relevantes para otimizar sua análise na indústria farmacêutica e farmpacia magistral de modo a garantir a qualidade do produto já comercializado. A proposta deste projeto foi desenvolver metodologias de análise para a cefoxitina sódica, fármaco comercializado no mercado médico-farmacêutico brasileiro. Foram desenvolvidos e validados métodos por CLAE com detector UV a 235 nm, com acetonitrila: água: ácido acético 5 M (22 : 78 : 1) como fase móvel e faixa de concentração de 20,0 à 30,0 μg/mL, tempo de retenção de 7,5 minutos. O coeficiente de correlação obtido foi de 0,9995 e a equação da reta y = 335,67x + 2391,9. O teste recuperação média obtido foi de 100,50%, com desvio padrão de 1,70%. O teor médio... (Resumo completo, clicar acesso eletrônico abaixo)
Abstract: Sodium cefatoxin (CAS 33564-30-6), a cephalosporinic antibiotic, has a wider spectrum of activity against Gram-negative microrganisms than older cephalosporin. It is also efficient against the indol-positive Proteus and Serratia and has a high resistance to b- lactamases hydrolysis. Sodium cefatoxin is recommended for the treatment of peritonitis and other intra-abdominal and intra-pelvic infections; sinusitis, gynecological infections, septicemy, endocarditis; urinary tract infections, non-complicated gonorrhea, respiratory tract infections, bones, articulations and skin. Although this drug has been strongly studied and many researches have been developed about its antibiotics activity, pharmacokinetics and pharmacodynamics, there are few studies in the literature about the development of analytical methodology to this cephalosporin. Researches dealing with analytical methods are extremely important and highly relevant to optimize its analysis at the pharmaceutical industry and manipulation pharmacy, guaranteeing quality of the commercialized product. This project proposes the development of methodologies for analysis of sodium cefatoxin, a commercialized drug at the medical-pharmaceutical Brazilian market. Methods for CLAE with UV detector at 235nm were developed and validated with acetonitrile: water: acetic acid 5M (22: 78:1) as mobile phase and concentration range of 20.0 to 30.0 μg/mL, detention time of 7.5 minutes. The correlation coefficient obtained was 0.9995 and the line equation y = 335.67x + 2391.9. The medium recovery test was 100.50% with standard deviation of 1.70%. The medium content of sodium cefoxitin determined by CLAE... (Complete abstract click electronic access below)
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Weiglová, Jana. "Možnosti využití energosádrovců a druhotných surovin obsahujících siřičitany pro přípravu kompozitů." Master's thesis, Vysoké učení technické v Brně. Fakulta chemická, 2010. http://www.nusl.cz/ntk/nusl-216617.

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The work studies the possibilities of the utilization of secondary raw materials produced by power industry. It addresses mainly the gypsum by-products and fluidized coal combustion ash. As for the secondary raw materials the content of sulphites is observed and the dependences of their transformation to sulphides via natural oxidation by air oxygen or by addition of adequate oxidant are studied. The work follows with describing the effect of sulphides contained in raw materials on the mechanical properties of composites prepared from several various matrices such as alumina or portland cement, lime or portland clinker. As for pure portland clinker the ability to retard the setting is also observed. The amount of contained sulphites is measured volumetrically via indirect titration of iodine surplus by sodium thiosulphate with the starch size as the indicator.
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Leitão, Rui Manuel Pereira Rodrigues. "Aplicação do método microiodométrico ao estudo das betalactamases de Bacteroides do grupo fragilis." Doctoral thesis, 1987. http://hdl.handle.net/10316/14532.

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Books on the topic "Iodometria"

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Wood, Delmer W. A detailed study of the iodometric determination of gas phase ozone. 1987.

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Book chapters on the topic "Iodometria"

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Burgot, Jean-Louis. "Oxidoreductimetry: Direct and Indirect Iodometries." In Ionic Equilibria in Analytical Chemistry, 313–45. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-8382-4_18.

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Burgot, Jean-Louis. "Iodometry in Alkaline Medium, Iodatometry, Periodimetry, and Bromometry." In Ionic Equilibria in Analytical Chemistry, 347–67. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-8382-4_19.

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Vasudevan, DM, and Subir Das. "Estimation of Amylase in Serum (Iodometric Method)." In Practical Textbook of Biochemistry for Medical Students, 80. Jaypee Brothers Medical Publishers (P) Ltd., 2013. http://dx.doi.org/10.5005/jp/books/12054_31.

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Gebicki, J. M., J. Collins, A. Baoutina, and P. Phair. "FAILURE OF AN AEROBIC IODOMETRIC PEROXIDE ASSAY." In Natural Antioxidants and Food Quality in Atherosclerosis and Cancer Prevention, 87–92. Elsevier, 1996. http://dx.doi.org/10.1533/9780857093059.87.

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Jessup, Wendy, Roger T. Dean, and Janusz M. Gebicki. "[29] Iodometric determination of hydroperoxides in lipids and proteins." In Methods in Enzymology, 289–303. Elsevier, 1994. http://dx.doi.org/10.1016/s0076-6879(94)33032-8.

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Dubey, Paras, and Netram Kaurav. "Stoichiometric and Nonstoichiometric Compounds." In Structure Processing Properties Relationships in Stoichiometric and Nonstoichiometric Oxides. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.89402.

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This chapter gives a general overview of synthesis and recent development of nickel oxide as a nonstoichiometric compound. We establish the synthesis chemistry of nickel oxide as a nonstoichiometric material, and hence successively introduce definitions and classifications of nonstoichiometric compounds as well as their point defects. The samples of nonstoichiometric nickel oxide are synthesized by thermal decomposition method. The nonstoichiometry of samples was then studied chemically by iodometric titration, and the results are further corroborated by excess oxygen obtained from the thermo-gravimetric analysis (TGA). X-ray diffraction (XRD) and Fourier transformed infrared (FTIR) techniques are used to analyze structural phase of nonstoichiometric nickel oxide. The change in oxidation state of nickel was studied by X-ray photoelectron spectroscopy (XPS) analysis. The shift in antiferromagnetic ordering and transition temperature due to nonstoichiometry is studied by magnetic and specific heat capacity analysis.
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Ivanova, I. I., A. D. Kazenina, B. V. Romanovsky, and I. M. Gerzeliev. "Application of iodometry for zeolite active sites characterization and modification." In Studies in Surface Science and Catalysis, 717–24. Elsevier, 1994. http://dx.doi.org/10.1016/s0167-2991(08)64178-6.

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Conference papers on the topic "Iodometria"

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Dinca, Mirela-Nicoleta, Mariana Ferdes, Bianca-Stefania Zabava, and Irina-Aura Istrate. "UV absorption spectra, Iodometric determination and pH variation in ozonated water using ozone generator." In 17th International Scientific Conference Engineering for Rural Development. Latvia University of Agriculture, 2018. http://dx.doi.org/10.22616/erdev2018.17.n388.

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Alauddin, M., L. V. Vigdorchik, S. A. Akbar, Z. A. Chaudhury, W. D. Ehmann, and B.-F. Ni. "Determination of oxygen contents of Bi1.9−xPbxSb0.1Sr2Ca2Cu3Oy by iodometry and its relevance to superconducting transition." In Superconductivity and its applications. AIP, 1992. http://dx.doi.org/10.1063/1.43578.

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