Relevant bibliographies by topics / Peracid

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Peracid'

Author: Grafiati
Published: 18 May 2024

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Journal articles on the topic "Peracid"

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Patil, Vilas Venunath, and Ganapati Subray Shankarling. "Nonanebis(peroxoic acid): a stable peracid for oxidative bromination of aminoanthracene-9,10-dione." Beilstein Journal of Organic Chemistry 10 (April 24, 2014): 921–28. http://dx.doi.org/10.3762/bjoc.10.90.

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A new protocol for the oxidative bromination of aminoanthracene-9,10-dione, which is highly deactivated towards the electrophilic substitution is investigated. The peracid, nonanebis(peroxoic acid), possesses advantages such as better stability at room temperature, it is easy to prepare and non-shock sensitiv as compared to the conventional peracids. The present protocol has a broad scope for the bromination of various substituted and unsubstituted aminoanthracene-9,10-diones.
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Pikh, Zoryan. "Oxidation of unsaturated aldehydes by different oxidants." Chemistry & Chemical Technology 1, no. 2 (June 15, 2007): 61–69. http://dx.doi.org/10.23939/chcht01.02.061.

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The new data about oxidation of unsaturated aldehydes of a general structure R–CH = C(R)–CHO by molecular oxygen (in liquid and gaseous phase), peracids and hydrogen peroxide were obtained. The composition of reaction products for a series of aldehydes with different structures was determined. The dependencies of the selectivity of reaction from an aldehyde structure and oxidant type have been evaluated. It has been assumed that a stage of aldehyde interaction with peracid determines the formation of reaction products. The common mechanisms of unsaturated aldehydes oxidation by different oxidants have been established on the basis of generalization of obtained results.
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Armstrong, Alan, Paul A. Barsanti, Paul A. Clarke, and Anthony Wood. "Ketone-directed peracid epoxidation." Tetrahedron Letters 35, no. 33 (August 1994): 6155–58. http://dx.doi.org/10.1016/0040-4039(94)88103-0.

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Minning, Stefan, Albrecht Weiss, Uwe T. Bornscheuer, and Rolf D. Schmid. "Determination of peracid and putative enzymatic peracid formation by an easy colorimetric assay." Analytica Chimica Acta 378, no. 1-3 (January 1999): 293–98. http://dx.doi.org/10.1016/s0003-2670(98)00612-6.

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Bouzid, Mouna, Hassen Ben Salah, and Majed Kammoun. "Peracid Oxidation of Dihydroisoquinoline Iminium." Asian Journal of Organic and Medicinal Chemistry 3, no. 3 (2018): 121–25. http://dx.doi.org/10.14233/ajomc.2018.ajomc-p148.

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Hassan, Suriaya, Abdul Ansari, Arvind Kumar, Munna Ram, Sulaxna Sharma, and Awanish Sharma. "Corrosion Resistance of Electroless Ni-P-W/ZrO<sub>2</sub> Nanocomposite Coatings in Peracid Solutions." Materials Science Forum 1048 (January 4, 2022): 72–79. http://dx.doi.org/10.4028/www.scientific.net/msf.1048.72.

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In current investigation, the Ni-P-W/ZrO2 electroless nanocomposite coatings are deposited upon mild steel substrate (AISI 1040 grade). The W/ZrO2 nanoparticles (50 to 130 nm range) were incorporated separately into acidic electroless Ni-P matrix as a second phase materials. The as-plated EL Ni-P-W/ZrO2 depositions were also heated at 400 οC in Argon atmosphere for one hour duration and analyzed by SEM/EDAX and XRD physical methods. The Ni-P-W/ZrO2 as-plated coupons revealed nebulous type structures while heated coupons showed crystalline structures in both cases. Furthermore Ni-P-ZrO2 coatings have very less cracks and gaps as compared to Ni-P-W coatings. The corrosion tests result in peracid (0.30 ± 0.02 % active oxygen) solutions point up that corrosivity of peracid ( 500 ppm Cl) is more than peracid (0 ppm Cl) and corrosion resistance of tested coupons varies as Ni-P-ZrO2 (as-plated) > Ni-P-ZrO2 (heated) > Ni-P-W (as-plated) > Ni-P-W (heated) > MS. The utilization of Ni-P-ZrO2 nanocomposite coatings in peracid solutions can be considered a cost effective option on the basis of its better cost/strength ratio in addition to its fair corrosion resistance.
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Buggle, Katherine, and Bernadette Fallon. "Peracid oxidation of benzothiopyranthiones and benzopyranthiones." Monatshefte f�r Chemie Chemical Monthly 118, no. 10 (October 1987): 1197–99. http://dx.doi.org/10.1007/bf00811293.

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ARMSTRONG, A., P. A. BARSANTI, P. A. CLARKE, and A. WOOD. "ChemInform Abstract: Ketone-Directed Peracid Epoxidation." ChemInform 26, no. 1 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199501079.

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Kim, Kwang-Seo, Jeffrey G. Pelton, William B. Inwood, Ulla Andersen, Sydney Kustu, and David E. Wemmer. "The Rut Pathway for Pyrimidine Degradation: Novel Chemistry and Toxicity Problems." Journal of Bacteriology 192, no. 16 (April 16, 2010): 4089–102. http://dx.doi.org/10.1128/jb.00201-10.

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ABSTRACT The Rut pathway is composed of seven proteins, all of which are required by Escherichia coli K-12 to grow on uracil as the sole nitrogen source. The RutA and RutB proteins are central: no spontaneous suppressors arise in strains lacking them. RutA works in conjunction with a flavin reductase (RutF or a substitute) to catalyze a novel reaction. It directly cleaves the uracil ring between N-3 and C-4 to yield ureidoacrylate, as established by both nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry. Although ureidoacrylate appears to arise by hydrolysis, the requirements for the reaction and the incorporation of 18O at C-4 from molecular oxygen indicate otherwise. Mass spectrometry revealed the presence of a small amount of product with the mass of ureidoacrylate peracid in reaction mixtures, and we infer that this is the direct product of RutA. In vitro RutB cleaves ureidoacrylate hydrolytically to release 2 mol of ammonium, malonic semialdehyde, and carbon dioxide. Presumably the direct products are aminoacrylate and carbamate, both of which hydrolyze spontaneously. Together with bioinformatic predictions and published crystal structures, genetic and physiological studies allow us to predict functions for RutC, -D, and -E. In vivo we postulate that RutB hydrolyzes the peracid of ureidoacrylate to yield the peracid of aminoacrylate. We speculate that RutC reduces aminoacrylate peracid to aminoacrylate and RutD increases the rate of spontaneous hydrolysis of aminoacrylate. The function of RutE appears to be the same as that of YdfG, which reduces malonic semialdehyde to 3-hydroxypropionic acid. RutG appears to be a uracil transporter.
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Parbat, Papiya, Alka Devi, and Vikas D. Ghule. "Computational assessment of nitrogen-rich peracids: a family of peroxide-based energetic materials." RSC Advances 7, no. 35 (2017): 21585–91. http://dx.doi.org/10.1039/c7ra02201h.

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Dissertations / Theses on the topic "Peracid"

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Paradis, Paul M. "Effect of surfactants on acyl and oxygen transfer : peracid reactivity and solution properties." Thesis, Northumbria University, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.367422.

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Lang, André Passaretti. "Estudo de perácidos intermediários da reação peróxi-oxalato." Universidade de São Paulo, 2008. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-30072009-144659/.

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O sistema quimiluminescente peróxi-oxalato vem sendo estudado por diversos grupos de pesquisa ao redor do mundo desde os anos 60. Esse interesse em especial se deve ao fato de que em comparação com a maioria dos sistemas quimiluminescentes, que apresentam rendimentos quânticos da ordem de 1%, esse sistema apresenta rendimentos quânticos de emissão consideravelmente maiores, cerca de 30%. O sistema peróxi-oxalato consiste na reação de ésteres fenólicos substituídos derivados do ácido oxálico com peróxido de hidrogênio, catalisada por uma base e em presença de compostos aromáticos policondensados fluorescentes com baixo potencial de oxidação, chamados de ativadores (ACT). O mecanismo desta reação, apesar de intensamente estudado, ainda não se encontra completamente esclarecido. Especificamente, a estrutura do intermediário formado durante a reação, que é responsável pela quimiexcitação do ativador, não é conhecida ainda. No presente trabalho, foram completados estudos previamente efetuados no nosso grupo com derivados perácidos, intermediários na reação peróxi-oxalato. Foram sintetizados e caracterizados dois novos derivados perácido, o O,Ohidrogênio monoperóxi-oxalato de 3-clorofenila e o O,O-hidrogênio monoperóxioxalato de 3-nitrofenila. Dos estudos cinéticos da reação destes perácidos com imidazol, na presença de 9,10-difenilantraceno como ativador, foram obtidos constantes de velocidade de ciclização e rendimentos quânticos singlete. As constantes de velocidade determinadas, junto com os dados obtidos anteriormente no grupo, mostram correlação linear de energia livre com as constantes de substituintes de Hammett, obtendo-se um valor de = 2,18 ± 0,16, o que indica a formação de alta densidade de carga negativa no estado de transição do passo lento. A correlação linear entre as constantes de velocidade e os valores de pKa dos grupos de partida fenólicos levou à determinação do valor de βGP = -1,07 ± 0,08, indicando que a quebra da ligação para o grupo de partida é muito avançada no estado de transição no passo lento da reação. Os rendimentos quânticos singlete mostram dependência com as propriedades eletrônicas dos substituintes, aumentando inicialmente com o aumento das propriedades de atração de elétron do substituinte, porém, com substituintes mais atraentes que hidrogênio, observa-se uma leve diminuição no rendimento quântico. O conjunto de dados apresentados neste trabalho, junto com os resultados obtidos anteriormente pelo grupo, demonstra claramente que a reação de ciclização dos perácidos, catalisada por imidazol, deve ocorrer de maneira concertada, ou seja, a saída do grupo de partida fenólico ocorre em conjunto com o ataque nucleofílico do íon percarboxilato à função éster no passo lento da reação. Conseqüentemente, foram obtidas neste trabalho evidências experimentais fundamentadas para a ocorrência da 1,2- dioxetanodiona como intermediário de alta energia na reação peróxi-oxalato.
The peroxyoxalate chemiluminescence has been intensely studied since the sixties by several research groups all around the world. This interest is mainly due to the fact that the peroxyoxalate system is highly efficient, showing quantum yields of around 30 %, much higher than other well known chemiluminescence reactions which commonly show quantum yields of around 1% or less. The peroxyoxalate system consists in the base catalyzed reaction of activated oxalate esters with hydrogen peroxide in the presence of highly fluorescent polycondensed aromatic hydrocarbons with low oxidation potentials, called activators (ACT). Although intensely investigated, the mechanism of this complex transformation is still not yet completely clarified. This is true specifically for the structure of the high-energy intermediate, formed during the reaction sequence, which is responsible for chemiexcitation, not known at all up to now. In the present work, former studies of our group on peracid derivatives, intermediates in the peroxyoxalate reaction, were completed. Two new peracid derivatives, 3-chlorophenyl O,O-hydrogen monoperoxyoxalate and 3- nitrophenyl O,O-hydrogen monoperoxyoxalate were synthesized and characterized. Kinetic studies on the reaction of these peracid derivatives with imidazole, in the presence of 9,10-diphenylanthracene as activator, led to the determination of cyclization rate constants and singlet quantum yields. These rate constants, together with data formerly obtained by our group, show linear free-energy correlation with the Hammett substituent constants, resulting in a reaction constant of = 2,18 ± 0,16, that indicates the formation of a high negative charge density in the transition state of the rate-limiting step. Similarly, the linear correlation of the rate constants with the pKa values of the phenolic leaving groups leads to the determination of a value βGP = -1,07 ± 0,08, indicating a high degree of leaving group bond cleavage in the transition state of the rate-limiting step. The singlet quantum yields also show dependence on the electronic properties of the substituents, initially increasing with the increase in the electron withdrawing nature of the substituent, however, a slight decrease in the quantum yields is observed with substituents more electron withdrawing than hydrogen. The data accumulated in this work, together with results earlier obtained in our group, clearly demonstrate that the cyclization reaction of the peracid derivatives, catalyzed by imidazole, proceeds in a concerted manner, i.e. the phenolic leaving group departure occurs together with the nucleophilic percarboxylate attach to the ester function in the rate-limiting reaction step. Consequently, it was possible to obtain in this work solid experimental evidence for the occurrence of 1,2-dioxetandione as the high-energy intermediate in the peroxyoxalate reaction.
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Smith, David P. "Characterisation of peracids." Thesis, University of Cambridge, 1996. https://www.repository.cam.ac.uk/handle/1810/272276.

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Feeder, Neil. "The crystal chemistry of organic peracids." Thesis, University of Cambridge, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.260610.

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Sechi, Gianluca. "Synthesis and applications of polymer supported peracids." Thesis, University of Edinburgh, 2009. http://hdl.handle.net/1842/11906.

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In recent years, polymer-assisted solution-phase synthesis has become a prevalent method because of its various advantages over conventional solution-phase chemistry, such as the ease of separation of the supported species from a reaction mixture by filtration and washing, the opportunity to use an excess of the reagent to force the reaction to completion, and the adaptability to continuous-flow processes. Peroxycarboxylic acids are common oxidants in a wide range of chemical transformations, but their use is often limited because of the associated handling risks. Some relatively stable peracids, such as meta-chloroperoxybenzoic acid, are commercially available, but quenching of unreacted species followed by extractions and/or chromatography separation is often required. The immobilisation of this type of reagent on a solid support can offer distinct advantages with respect to handling and stability. Carboxylic ion-exchange resins, such as acrylic macroporous matrix, can be oxidised to give highly functionalised supported peroxycarboxylic acids. The polymer-supported peracid generated from Dowex MAC-3® proved to be the best in terms of oxidation capacity among the supports and reaction conditions tested. The new high-loading polymer-supported peracid was stable under standard laboratory practice, also when it was crushed or heated, and it was used successfully in the oxidation of sulfides, alkenes, and pyridines, giving the products with high yields and purities without the need for any additional purification step.
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Delagoutte, Thierry. "Evaluation des péroxyacides (acide péroxyacétique et acide péroxymonosulfurique) en tant qu'agents de blanchiment des pâtes à papier chimiques kraft." Grenoble INPG, 1998. http://www.theses.fr/1998INPG0020.

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L'etude realisee entre dans le cadre de la recherche de nouveaux reactifs non chlores pour le blanchiment papetier. Deux peroxyacides ont ete evalues : l'acide peroxyacetique et l'acide peroxymonosulfurique. La premiere partie a ete consacree a l'optimisation des procedes de blanchiment. Differents aspects de l'usage de ces reactifs en application au blanchiment des pates a papier chimiques kraft ont ete envisages. Ces travaux montrent que les peroxyacides sont des agents de blanchiment efficaces pouvant etre utilises pour la delignification de pates cellulosiques a fortes teneurs en lignine, comme pour parfaire la decoloration de pates comportant de faibles taux de lignine residuelle. Une application industielle a pu voir le jour decoulant de ces travaux. La seconde partie, a developpe l'etude de la caracterisation de lignines residuelles issues de pates traitees par les peroxyacides. Ce travail constitue en fait une reponse a des travaux anterieurs a cette these, sur l'effet activateur des peroxyacides. Les resultats obtenus par mesure en rmn#1#3c montrent que, contrairement au modele propose pour interpreter cet effet, les lignines issues des pates traitees ne presentent pas un enrichissement en unites phenoliques. En revanche, une reduction sensible de la teneur en unites aromatiques totales, assortie d'une conservation du ratio groupements phenoliques / groupements aromatiques totaux a ete note. Par ailleurs, les lignines residuelles se sont enrichies en groupements carboxyliques. Enfin, la troisieme partie, a etudie l'action de certains cations metalliques sur les peroxyacides. Ainsi, les peroxyacides sont decomposes catalytiquement par les metaux les plus couramment rencontres dans les pates, tels le fer ou le cuivre. De plus, les mecanismes de decomposition peuvent conduire a la generation de radicaux hydroxyles nefastes pour la qualite de la cellulose. D'autre part, l'etude de l'influence du cobalt s'est averee interessante, dans la mesure ou ce metal decompose efficacement les peroxyacides en conduisant a la generation d'especes sans consequence pour la cellulose, mais tres actives pour oxyder des molecules modeles de lignine. Ce point ouvre un champ d'applications potentiel des peroxyacides en blanchiment, en presence d'activateurs tels le cobalt ou encore les complexes de celui-ci.
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Magri, Annarita. "La setta dei Perati." Paris, EPHE, 2007. http://www.theses.fr/2007EPHE5012.

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L’étude est consacrée au groupe religieux des Pérates, décrit dans la « Refutatio omnium haeresium V, 12-18 » et autrement peu connu. La thèse est partagée en trois parties : une première concernant l’exégèse du groupe, basée sur des « testimonia crucis et ligni » et sur le renversement de plusieurs figures bibliques négatives (Caïn, Esaü, Nimrod), une procédure appelée « Protestexegese » ; une analyse des matériaux païens recueillis par la secte parmi les cultes à mystères ou polythéistes, surtout en rapport avec l’adoration du serpent et l’astrologie ; une tentative de situer le groupe en Asie Mineuse et d’en offrir une perspective sociologique. Les résultats de la recherche permettent d’en montre l’origine chrétienne, même si les éléments chrétiens ont été mélangés d’une façon syncrétiste avec la philosophie grecque, les cultes à mystères, l’astrologie et d’autres composantes ; la connaissance de l’exégèse et de la culture juive par les appartenants au groupe permet de montrer une probable origine à l’intérieur des églises chrétiennes de la disapora, entre Ier et IIème siècles
This work studies the sect of the Perates, which is described in the Refutatio omnium haeresium V, 12-18 and which is otherwise very little known. The study is divided into 3 main parts : an assessment of the exegesis of the group, founded on a series of “testimonia crucis et ligni”, and on the reversal of some negative figure of the Bible (Cain, Esau, Nimrod), a procedure usually called Protestexegese ; an analysis about the materials gathered by the sect in heathen cults and religions, above all the adoration of the serpent and astrology ; a trial to place the group in the “milieu” of Asia Minor and of a sociological assessment. The results of the research allow to point to a Christian origin of the sect, even if the Christian elements have been syncretistically mixed with Greek philosophy, mystery cults, astrology, and other components ; the knowledge of Jewish exegesis and culture by the sectarians shows a likely origin inside the Christian churches born in the Diaspora among Ist and IInd centuries
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Reischle, Ekkehard Hendrik. "Perazin - ein "typisches" Antipsychotikum mit "atypischem" Nebenwirkungsprofil? : ein Vergleich der Häufigkeit der Behandlung von extrapyramidalen Nebenwirkungen zwischen Risperidon, Olanzapin und Perazin." kostenfrei, 2008. http://www.opus-bayern.de/uni-regensburg/volltexte/2009/1213/.

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Klánský, Lukáš. "Murray Perahia a jeho přínos klavírní in terpretaci." Master's thesis, Akademie múzických umění v Praze.Hudební a taneční fakulta. Knihovna, 2015. http://www.nusl.cz/ntk/nusl-202865.

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This Master Thesis deals with the world-renowned pianist Murray Perahioa and his contribution to the pianist. It describes his life and introduces readers to his views on music. It is analyzing his recordings and focuses on his editorial activity also. Analysis of the recordings is centered on important works of the Baroque and Classica era. Analysis of editorial work is conceived as another way to understand the weork of the extraordinary pianist.
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Griffiths, David P. "Trying to decrease the decomposition rates of peracids (and Hâ‚‚Oâ‚‚) by solution-phase metal ions." Thesis, University of York, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.423842.

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Books on the topic "Peracid"

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Perazić, Tomislav. Perazić. Zenica: Naša riječ, 2009.

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1947-, Sánchez Enriquillo, and Santos, José Andrés de los., eds. Peravia. [Santo Domingo?]: BanReservas, 2003.

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Simon, Hasida. Peraḥim le-khol ʻet: Sidure peraḥim Yiśreʼeliyim. [Tel Aviv]: Miśrad ha-biṭaḥon, 1998.

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Hirsh-Noi, Mikhal. Peraḥim meluḥim. T.A. [z.o. Tel Aviv]: Tamuz, 1988.

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ʻEran, Ḳlain, Nachmias David, and Makhon ha-Yiśreʾeli le-demoḳraṭyah, eds. Ḥaḳiḳah peraṭit. Yerushalayim: Makhon ha-Yiśreʾeli le-demoḳraṭyah, 2002.

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Carmel, Adi. Ḥelḳah peraṭit. [Tel Aviv]: Reshafim, 1987.

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Vita peracta. Buenos Aires, República Argentina: Ediciones Ultimo Reino, 2003.

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Periḥah peraʾit. Yerushalayim: Keter, 2004.

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Carmel, Adi. Ḥelḳah peraṭit. [Tel Aviv]: Reshafim, 1987.

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Yaron, Emunah. Peraḳim me-ḥayai. Yerushalyim: Shoḳen, 2005.

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Book chapters on the topic "Peracid"

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Benkert, Otto, Ion Anghelescu, Christoph Fehr, Gerhard Gründer, Philip Heiser, Christoph Hiemke, Christian Lange-Asschenfeldt, et al. "Perazin." In Pocket Guide Psychopharmaka von A bis Z, 191–93. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-01910-4_85.

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Beyer, Karl-Heinz. "Perazin." In Biotransformation der Arzneimittel, 431–32. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-74386-3_247.

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Musall, Frederek. "Maimonides: Schemona Perakim." In Kindlers Literatur Lexikon (KLL), 1–2. Stuttgart: J.B. Metzler, 2020. http://dx.doi.org/10.1007/978-3-476-05728-0_16223-1.

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Thiel, Martin. "Chemical Communication in Peracarid Crustaceans." In Chemical Communication in Crustaceans, 199–218. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-0-387-77101-4_10.

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Siedel, George. "MIT Operations Professor Georgia Perakis." In Seven Essentials for Business Success, 137–56. New York: Routledge, 2021. http://dx.doi.org/10.4324/9781003187318-8.

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Müller-Oerlinghausen, B. "Drei Fälle von Priapismus unter Perazin." In Verhandlungen der Deutschen Gesellschaft für Innere Medizin, 723. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-83864-4_143.

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Fossey, Jacques, Daniel Lefort, and Janine Sorba. "Peracids and free radicals: A theoretical and experimental approach." In Organic Peroxygen Chemistry, 99–113. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/3-540-56252-4_27.

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Poppius-Levlin, K., A. S. Jääskeläinen, A. Seisto, and A. Fuhrmann. "Peracids in Kraft Pulp Bleaching: Past, Present, and Future." In ACS Symposium Series, 471–89. Washington, DC: American Chemical Society, 1999. http://dx.doi.org/10.1021/bk-2000-0742.ch024.

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Kakaraparthi, Vishnu, Troy McDaniel, Hemanth Venkateswara, and Morris Goldberg. "PERACTIV: Personalized Activity Monitoring - Ask My Hands." In Lecture Notes in Computer Science, 255–72. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-05431-0_18.

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Vanderwees, Chris. "Speaking of François Peraldi in Québec in Four Parts." In On the History and Transmission of Lacanian Psychoanalysis, 57–96. London: Routledge, 2023. http://dx.doi.org/10.4324/9781003323136-5.

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Conference papers on the topic "Peracid"

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Habri, Hamzah Hafizuddin, Mohd Jumain Jalil, Intan Suhada Azmi, Pascal Perrin Anak Jites, Mohamad Heiry Mohd Azmi, and Danial Nuruddin Azlan Raofuddina. "Epoxidation of oleic acid from vegetable oil by peracid mechanism." In INTERNATIONAL CONFERENCE ON TRENDS IN CHEMICAL ENGINEERING 2021 (ICoTRiCE2021). AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0113009.

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Balasubramanian, Ramakrishnan, Junzhong Li, Irwan Yunus, Timothy J. Tidwell, Victor Keasler, and Richard Staub. "A Next Generation Peracid for Onshore and Offshore Water Treatment Applications." In SPE International Conference on Oilfield Chemistry. Society of Petroleum Engineers, 2017. http://dx.doi.org/10.2118/184560-ms.

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Balasubramanian, Ramakrishnan, Robert Ryther, Renato De Paula, Brian Epps, Victor Keasler, Junzhong Li, and Richard Staub. "Development Of A Very Low Peroxide Containing Peracid Formulation As Superior Treatment Option For Water Reuse Applications." In SPE International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 2015. http://dx.doi.org/10.2118/173780-ms.

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4

"PerAI-6G Committee." In IEEE INFOCOM 2022 - IEEE Conference on Computer Communications Workshops (INFOCOM WKSHPS). IEEE, 2022. http://dx.doi.org/10.1109/infocomwkshps54753.2022.9798373.

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"PerAI-6G Committee." In IEEE INFOCOM 2023 - IEEE Conference on Computer Communications Workshops (INFOCOM WKSHPS). IEEE, 2023. http://dx.doi.org/10.1109/infocomwkshps57453.2023.10226050.

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"PerAI-6G 2022 Program." In IEEE INFOCOM 2022 - IEEE Conference on Computer Communications Workshops (INFOCOM WKSHPS). IEEE, 2022. http://dx.doi.org/10.1109/infocomwkshps54753.2022.9798324.

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"PerAI-6G 2022 TPC." In IEEE INFOCOM 2022 - IEEE Conference on Computer Communications Workshops (INFOCOM WKSHPS). IEEE, 2022. http://dx.doi.org/10.1109/infocomwkshps54753.2022.9798363.

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"Perai-6G 2023 Program." In IEEE INFOCOM 2023 - IEEE Conference on Computer Communications Workshops (INFOCOM WKSHPS). IEEE, 2023. http://dx.doi.org/10.1109/infocomwkshps57453.2023.10225981.

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9

"Proceedings of PerAc '94. From Perception to Action." In Proceedings of PerAc '94. From Perception to Action. IEEE, 1994. http://dx.doi.org/10.1109/fpa.1994.636075.

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Rumbold, C. E., N. Battini, C. B. Giachetti, K. L. Castro, S. Obenat, and E. Schwindt. "DIVERSITY OF NATIVE AND EXOTIC PERACARID SPECIES IN MARINE PORTS OF SOUTHWESTERN ATLANTIC." In X Congresso Brasileiro sobre Crustáceos. Sociedade Brasileira de Carcinologia, 2018. http://dx.doi.org/10.21826/2178-7581x2018068.

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