Academic literature on the topic 'Piperazino'

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Journal articles on the topic "Piperazino"

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Vejdělek, Zdeněk, and Miroslav Protiva. "N-(piperazinoacyl) and N-(piperazinoalkyl) derivatives of 4-cyclopentylaniline and related compounds: Synthesis and pharmacological screening." Collection of Czechoslovak Chemical Communications 51, no. 7 (1986): 1494–502. http://dx.doi.org/10.1135/cccc19861494.

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Five N-(4-cyclopentylphenyl)haloalkanecarboxamides were reacted with 1-methylpiperazine and 1-(2-hydroxyethyl)piperazine to give the corresponding N-(4-cyclopentylphenyl)piperazinoalkanecarboxamides Iab -Vab. Their reduction with lithium aluminium hydride afforded the triamines VIIab - XIab. Acylation of the N-(4-methylpiperazino)alkyl-4-cyclopentylanilines Xa and XIa with propionyl chloride resulted in the propionanilides XIVa and XVa, whereas a similar reaction of the N-(4-(2-hydroxyethyl)piperazino)alkyl-4-cyclopentylanilines VIIb and IXb - XIb produced the propionoxypropionanilides XIIc -
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Kmoníček, Vojtěch, Martin Valchář, and Zdeněk Polívka. "Some 4-Substituted 1-(3-Pyridylmethyl)piperazines with Antihistamine Activity." Collection of Czechoslovak Chemical Communications 59, no. 10 (1994): 2343–50. http://dx.doi.org/10.1135/cccc19942343.

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Several compounds derived from nicotinic acid were prepared within a more extensive programme aiming at the synthesis of new substances with expected antihistamine and antidepressant activity. Some of these compounds display certain structural resemblance with the antidepressant agent piberaline (EGYT 475, Trelibet®, I) and its analogues. The products were used as intermediates for the synthesis of further compounds and most of them were subjected to pharmacological testing. Substituted nicotinic acid piperazides IIa - IId and IVa - IVe were obtained by reactions of nicotinoyl chloride (prepar
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Gettys, Kristen, Zhishi Ye, and Mingji Dai. "Recent Advances in Piperazine Synthesis." Synthesis 49, no. 12 (2017): 2589–604. http://dx.doi.org/10.1055/s-0036-1589491.

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Piperazine ranks as the third most common N-heterocycle appearing in small-molecule pharmaceuticals. This review highlights recent advances in methods development for the construction of the piperazine­ ring system with particular emphasis on preparing carbon-substituted piperazines.1 Introduction2 Reduction of (Di)ketopiperazine3 N-Alkylation4 Transition-Metal-Catalyzed/Mediated Piperazine Synthesis4.1 The SnAP and SLAP Methods4.2 Palladium-Catalyzed Cyclization4.3 Gold-Catalyzed Cyclization4.4 Other Metal-Catalyzed/Mediated Cyclization4.5 Borrowing Hydrogen Strategy4.6 Imine Reductive Cycliz
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Jílek, Jiří, Jiří Holubek, Emil Svátek, et al. "Potential metabolites of the neuroleptic agents belonging to the 8-methylthio-10-piperazino-10,11-dihydrodibenzo[b,f]thiepin series; Synthesis of 2-hydroxy and 3-hydroxy derivatives." Collection of Czechoslovak Chemical Communications 50, no. 10 (1985): 2179–90. http://dx.doi.org/10.1135/cccc19852179.

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The acid VI, prepared by reaction of potassium salts of (2-iodo-5-methoxyphenyl)acetic acid and 4-(methylthio)thiophenol in the presence of copper, was transformed via intermediates VII-IX to 2-methoxy-8-methylthio-10-piperazino-10,11-dihydrodibenzo[b,f]thiepins X and XI. Their demethylation with boron tribromide afforded 2-hydroxy derivatives of the neuroleptic agents methiothepin and oxyprothepin I and II. 11-Chloro-7-methoxy-2-methylthio-10,11-dihydrodibenzo[b,f]thiepin was subjected to substitution reactions with 1-methylpiperazine and 1-(ethoxycarbonyl)piperazine and gave piperazine deriv
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Lawson, Edward C., Diane K. Luci, Shyamali Ghosh, et al. "Nonpeptide Urotensin-II Receptor Antagonists: A New Ligand Class Based on Piperazino-Phthalimide and Piperazino-Isoindolinone Subunits." Journal of Medicinal Chemistry 52, no. 23 (2009): 7432–45. http://dx.doi.org/10.1021/jm900683d.

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Lou, Chenguang, Birte Vester, and Jesper Wengel. "Oligonucleotides containing a piperazino-modified 2′-amino-LNA monomer exhibit very high duplex stability and remarkable nuclease resistance." Chemical Communications 51, no. 19 (2015): 4024–27. http://dx.doi.org/10.1039/c5cc00322a.

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Incorporation of a novel piperazino-modified 2′-amino-LNA monomer (PipLNA-T) into oligonucleotides leads to a pronounced affinity increase against complementary DNA and RNA and a strong stabilising effect against 3′-exonucleolytic degradation.
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Pandey, Anubhuti, Sarvesh Kumar Paliwal, and Shailendra Kumar Paliwal. "Chemical Feature-Based Molecular Modeling of Urotensin-II Receptor Antagonists: Generation of Predictive Pharmacophore Model for Early Drug Discovery." Journal of Chemistry 2014 (2014): 1–16. http://dx.doi.org/10.1155/2014/921863.

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For a series of 35 piperazino-phthalimide and piperazino-isoindolinone based urotensin-II receptor (UT) antagonists, a thoroughly validated 3D pharmacophore model has been developed, consisting of four chemical features: one hydrogen bond acceptor lipid (HBA_L), one hydrophobe (HY), and two ring aromatic (RA). Multiple validation techniques like CatScramble, test set prediction, and mapping analysis of advanced known antagonists have been employed to check the predictive power and robustness of the developed model. The results demonstrate that the best model, Hypo 1, shows a correlation (r) of
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Yadav, Pradeep, and Y. C. Joshi. "Synthesis and Spectral Study of Novel Norfloxacin Derivatives." E-Journal of Chemistry 5, s2 (2008): 1154–58. http://dx.doi.org/10.1155/2008/357073.

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Reaction of [1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-quinolone-3-carboxylic acid (norfloxacin) with thiazole / benzothiazole diazonium chloride to get new piperazine substituted norfloxacin derivative. These norfloxacin derivatives were further condensed with variousβ-diketone to get novel acid derivatives of 1-Ethyl-6-fluoro-4-oxo-7- [4 (thiazol-2-yldiazenyl)-piperzin-1-yl]-1,4-dihydro-quinoline-3-carboxylic acid (6a-e) and 7-(4-(benzo[d]thiazol-2-yldiazenyl)piperazin-1-yl)-1-ethyl-6-fluoro-4-oxo-1, 4-dihydroquinoline-3-carboxylic acid (6 f-j). Structures of these compounds were
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Desai, Akshay D., and Kishor H. Chikhalia. "Synthesis and Studies of 1-[2-(Aryl Amino-2-Oxo Ethyl) Amino]-4-(N-Methyl Piperazino)-Benzene Derivatives." E-Journal of Chemistry 2, no. 1 (2005): 15–20. http://dx.doi.org/10.1155/2005/575290.

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1-[2-(Aryl Amino-2-Oxo Ethyl) Amino]-4-(N-Methyl Piperazino)-Benzene Derivatives were synthesized. The synthesized compounds were screened for their antibacterial activities againstS.auresandE.coliby cup plat method. From screening result some compounds found highly active against both Gram-positive and Gram-negative bacteria while other compounds possess feeble to moderate activity.
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Bogeso, Klaus P., Jorn Arnt, Kristen Frederiksen, Hans Otto Hansen, John Hyttel, and Henrik Pedersen. "Enhanced D1 Affinity in a Series of Piperazine Ring Substituted 1-Piperazino-3-Arylindans with Potential Atypical Antipsychotic Activity." Journal of Medicinal Chemistry 38, no. 22 (1995): 4380–92. http://dx.doi.org/10.1021/jm00022a004.

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Dissertations / Theses on the topic "Piperazino"

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MASHONDI, MOHAMED. "Synthese regiospecifique et regioselective d'aminosaccharides et de piperazino-saccharides a visee therapeutique." Amiens, 1996. http://www.theses.fr/1996AMIE0105.

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Ce travail decrit la synthese de deux familles d'aminosaccharides a visee therapeutique. La premiere gamme comprend des derives du d-galactose, du d-glucose, du d-xylose et du xylitol, sur lesquels ont ete greffes par l'intermediaire d'une jonction aminee, soit une chaine n-alkyle soit un groupement phenylalkyle. Trois methodes ont ete utilisees, sur le site anomerique ; condensation d'une amine primaire, sur les sites primaires : greffe du nh#3 ou de rnh#2 apres activation, sur les sites secondaires, d'abord preparation d'un aminosaccharide selon la sequence suivante, activation, azidation, r
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Bøgesø, Klaus P. "Drug hunting : the medicinal chemistry of 1-Piperazino-3-Phenylindans and related compounds /." Copenhagen : Medicinal Chemistry Research H. Lundbeck, 1998. http://www.gbv.de/dms/bs/toc/25247774X.pdf.

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Moura, Rebeca Garcia. "Síntese de um fragmento precursor do Indinavir." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-11042017-075910/.

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Considerando-se a necessidade brasileira de se obterem fármacos a preços competitivos e usando tecnologia nacional, visamos sintetizar um fragmento do Indinavir empregando como material de partida a L-serina, um aminoácido natural de baixo custo. Desta maneira, desenvolvemos a seguinte rota, em 6 etapas: p-tosilação da serina, pelo uso de cloreto de p-tosila / NaOH; amidação da p-tosilserina, empregando-se o sal de terc-butilamônio da N-hidroxissuccinimida / DCC; ciclização da (S)-2-terc-butil-N-p-tosilserina, em condição de transferência de fase, com cloreto de p-tosila / carbonato de potássi
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Khan, Abdul Majeed 1980. "Síntese e termoquímica de adutos de brometos de metais bivalentes com aminas hetrocíclicas." [s.n.], 2013. http://repositorio.unicamp.br/jspui/handle/REPOSIP/249123.

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Orientador: Pedro Oliver Dunstan Lozano<br>Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Química<br>Made available in DSpace on 2018-08-22T07:28:40Z (GMT). No. of bitstreams: 1 Khan_AbdulMajeed_D.pdf: 3004508 bytes, checksum: 1d8c778094bf0cb1b93fa7bf80e19074 (MD5) Previous issue date: 2013<br>Resumo: Os adutos MX2.nL (M = Mn, Fe, Co, Ni, Cu ou Zn, L = 3-cianopiridina, piperidina ou piperazaina, X = Br, n = 0,5, 0,75, 1, 1,5, 2 ou 4), foram sintetizados e caracterizados através de análise elementar, determinação de pontos de fusão, espectroscopia IV e eletrônica e análise
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Viana, Fernando Andrà Campos. "Estudo comparativo, randomizado para avaliar a eficÃcia terapÃutica da piperazina hexahidratada com extrato fluido de rhamnus purshiana no tratamento da ascaridÃase." Universidade Federal do CearÃ, 2007. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=646.

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Conselho Nacional de Desenvolvimento CientÃfico e TecnolÃgico<br>A eficÃcia e a seguranÃa terapÃutica de um medicamento a base de piperazina hexahidratada associada com o extrato fluido de Rhamnus purshiana (DM IndÃstria FarmacÃutica) usada como tratamento anti-helmÃntico em pacientes no CearÃ, Brasil, foi testado em comparaÃÃo com o produto composto de piperazina sem qualquer associaÃÃo (DM IndÃstria FarmacÃutica). Um estudo prospectivo, randomizado, controlado e duplo cego, comparando taxas de cura para infecÃÃo por Ascaris lunbricoides. Amostras coprolÃgicas de 990 pacientes foram coletadas
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Vasconcelos, Leonardo de. "Síntese de um fragmento precursor do fármaco Indinavir." Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-23042013-141617/.

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Neste trabalho foram aprofundados nossos estudos para obtenção da (S)-2-terc-butilamida-4-(3-picolil)piperazina, pela abertura da (S)-2-terc-butilcarboxamida-N-p-tosilaziridina seguida de ciclização, em 78% de rendimento, com o triflato de vinildifenilsulfônio. A aziridina foi preparada por um processo de ciclização, em condições de transferência de fase, partindo-se da L-serina, um aminoácido natural de baixo custo. Esta rota sintética rendeu um material que apresenta a mesma estereoquímica S do fragmento piperazínico usado na síntese do Indinavir, podendo vir a constituir uma via alternativa
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González, Lira Christian Guillermo. "Estudio de Funcionalización de la (4-Nitro-Fenil)-1-Piperazina Orientada a la Síntesis de (4,7-Dimetoxi-Benzo[b]Tiofen-2-Carbonil) Piperazinil Arilbenzamidas como Potenciales Ligandos Serotoninérgicos." Tesis, Universidad de Chile, 2007. http://www.repositorio.uchile.cl/handle/2250/105666.

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Memoria para optar al título de Químico<br>Las arilpiperazinas constituyen una familia de compuestos de interés en el ámbito neurofarmacológico principalmente por sus acciones ansiolíticas y antidepresivas, a través de interacciones con el receptor serotoninérgico 5-HT1A. El presente trabajo de tesis informa de la síntesis de una serie de compuestos benzotiofenarilpiperazínicos 10 (a-f) adecuadamente funcionalizados. El acceso sintético a esta serie tiene lugar a través de una secuencia de 6 pasos a partir de 3,6-dimetoxi-2-nitrobenzaldehído con tioglicolato de metilo en medio básico. Como p
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Monaghan, S. M. "Synthetic studies in the piperazine-2,5-dione area." Thesis, Imperial College London, 1987. http://hdl.handle.net/10044/1/47304.

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Uddin, Farid. "Use of piperazine ligands for bleaching and epoxidation catalysis." Thesis, Queen Mary, University of London, 2011. http://qmro.qmul.ac.uk/xmlui/handle/123456789/692.

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Following reports that the dinuclear manganese complex of the ligand 1, 4, 7-trimethyl-1, 4, 7-triazacyclononane (TMTACN) was a potent bleaching catalyst, its catalytic oxidative activity was thoroughly studied. Apart from its catalytic bleaching activity, it has shown to be a versatile catalyst in terms of its substrate scope. In bleaching, it still remains the benchmark with regards to its catalytic bleaching activity against which systems in development are compared. Chapter one discusses the need for a bleaching catalyst in detergent formulations and the advantages it offers over existing
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Kuleya, Chipo. "The synthesis, analysis and characterisation of piperazine based drugs." Thesis, Anglia Ruskin University, 2014. https://arro.anglia.ac.uk/id/eprint/579889/1/Thesis%20%20final%20-%20Chipo%20Kuleya%20July%202015.pdf.

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This study developed a GC-MS method for the simultaneous detection of piperazines and congeners in street samples of amphetamine type stimulants. This research investigated the clandestine routes of synthesis and chemical profiles of phenylpiperazines, represented by 1- (4-fluorophenyl)piperazine (4-FPP) and 1-(3-trifluoromethylphenyl)piperazine (3-TFMPP). These drugs are part of the increasingly prevalent illicit new psychoactive substances. The presence of (2, 3, 4) FPP and (2, 3, 4) TFMPP positional isomers has been identified by other researchers as a limitation due to their similar
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Books on the topic "Piperazino"

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Kagaku Busshitsu Hyōka Kenkyū Kikō and Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), eds. Piperajin: Piperazine. Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2007.

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Attorney-General, New Zealand. Report of the Attorney-General under the New Zealand Bill of Rights Act 1990 on the Misuse of Drugs (Classification of BZP) Amendment Bill 2007. House of Representatives, 2007.

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Great Britain. Health and Safety Executive. Occupational Medicine and Hygiene Laboratory. Organic isocyanates in air: Laboratory method using 1-(2-methoxyphenyl) piperazine solution and high performance liquid chromatography. HSE Books, 1994.

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Occupational Medicine and Hygiene Laboratory. Organic isocyanates in air: Laboratory method using 1-(2-methoxyphenyl) piperazine solution and high performance liquid chromatography. Health and Safety Executive, 1987.

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Sedefov, Roumen. Report on the risk assessment of BZP in the framework of the Council decision on new psychoactive substances. Office for Official Publications of the European Communities, 2009.

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1935-, Gingell Clive, ed. Management of ED: Focus on sildenafil : a urologist's approach. PharmaLibri, 1998.

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J, Fowler Clare, ed. Management of ED: Focus on sildenafil : a neurologist's approach. PharmaLibri, 1999.

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Botz-Bornstein, Thorsten. The philosophy of Viagra: Bioethical responses to the viagrification of the modern world. Rodopi, 2011.

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Bain, Joseph Paul 1914. Derivatives of Piperazine VIII: Synthesis of Substituted Piperazines and Reactions of Piperazines with Conjugated Systems. Creative Media Partners, LLC, 2021.

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Derivatives of Piperazine IV . . Creative Media Partners, LLC, 2021.

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Book chapters on the topic "Piperazino"

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de Groot, Anton C. "Piperazine." In Monographs In Contact Allergy. CRC Press, 2022. http://dx.doi.org/10.1201/9781003158004-391.

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Stark, Margaret, Jason Payne-James, and Michael Scott-Ham. "Piperazines." In Symptoms and Signs of Substance Use, 4th ed. Routledge, 2025. https://doi.org/10.4324/9781003381730-29.

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Hirota, E., K. Kuchitsu, T. Steimle, J. Vogt, and N. Vogt. "116 C4H10N2 Piperazine." In Molecules Containing Three or Four Carbon Atoms and Molecules Containing Five or More Carbon Atoms. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-41504-3_117.

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Alicante, Raquel. "Piperazine Azopolymer Thin Films." In Springer Theses. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-31756-9_4.

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Laux, Gerd. "Piperazine Phenothiazines: Fluphenazine and Perphenazine." In NeuroPsychopharmacotherapy. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-62059-2_474.

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Eller, Sarah, and Marcelo Dutra Arbo. "Piperazine Designer Drugs of Abuse." In Handbook of Substance Misuse and Addictions. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-92392-1_166.

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Laux, Gerd. "Piperazine Phenothiazines: Fluphenazine and Perphenazine." In NeuroPsychopharmacotherapy. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-319-56015-1_474-1.

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Eller, Sarah, and Marcelo Dutra Arbo. "Piperazine Designer Drugs of Abuse." In Handbook of Substance Misuse and Addictions. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-67928-6_166-1.

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Bährle-Rapp, Marina. "Diethylene Glycolamine/Epichlorohydrin/Piperazine Copolymer." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_2932.

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Kuleya, Chipo, and Michael D. Cole. "Forensic Analysis of Piperazines." In Chromatographic Techniques in the Forensic Analysis of Designer Drugs. CRC Press, 2018. http://dx.doi.org/10.1201/9781315313177-17.

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Conference papers on the topic "Piperazino"

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Akkor, Ilayda, Shachit S. Iyer, John Dowdle, Le Wang, and Chrysanthos Gounaris. "Economic Optimization and Impact of Utility Costs on the Optimal Design of Piperazine-Based Carbon Capture." In Foundations of Computer-Aided Process Design. PSE Press, 2024. http://dx.doi.org/10.69997/sct.147100.

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Recent advances in process design for solvent-based, post-combustion capture (PCC) processes, such as the Piperazine/Advanced Flash Stripper (PZ/AFS) process, have led to a reduction in the energy required for capture. Even though PCC processes are progressively improving in Technology Readiness Levels (TRL), with a few commercial installations, incorporating carbon capture adds cost to any operation. Hence, cost reduction will be instrumental for proliferation. The aim of this work is to improve process economics through optimization and to identify the parameters in our economic model that h
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Huang, Shengyuan, Olajide Otitoju, Yao Zhang, and Meihong Wang. "Technical Assessment of direct air capture using piperazine in an advanced solvent-based absorption process." In The 35th European Symposium on Computer Aided Process Engineering. PSE Press, 2025. https://doi.org/10.69997/sct.124483.

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Climate and environmental problems caused by increasing CO2 concentration in the atmosphere make the direct air capture (DAC) technology having great prospects for development. As the widely used solvent in carbon capture based on chemical absorption processes, MEA still fails to address the issues of high energy consumption and high costs when used in DAC process. In this study, piperazine (PZ) was used as the new solvent for DAC process. The new configuration was simulated in Aspen Plus� V11 and the model was validated through experimental data and model comparison. It is followed by investi
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Peng, Lei, Qiang Fu, Zhi Li, Musong Lin, Yaohong Zhao, and Zaikun Wu. "Investigate of mass transfer of CO2 absorption into the mixed solution of piperazine and diethanolamine in a packed column." In Fifth International Conference on Green Energy, Environment, and Sustainable Development, edited by Mohammadreza Aghaei, Hongyu Ren, and Xiaoshuan Zhang. SPIE, 2024. http://dx.doi.org/10.1117/12.3044925.

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Pazdera, P., B. Andělová, and D. Němečková. "Utilization of piperazine for interphase catalytic systems." In The 13th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00192.

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Loupias, Pauline, Alexandra Dassonville-Klimpt, Elodie Lohou, Nicolas Taudon, and Pascal Sonnet. "Trojan horse strategy: synthesis of piperazine-based siderophores." In 4th International Electronic Conference on Medicinal Chemistry. MDPI, 2018. http://dx.doi.org/10.3390/ecmc-4-05579.

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Zhang, Xiaoguang, Xuexing Chen, Qingchun Chen, et al. "Preparation and Co (II) Removal of ZnO/Poly-Piperazineamide Nanofiltration Membranes." In 2017 25th International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/icone25-67740.

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A series of nanofiltration membranes were prepared by interfacial polymerization of piperazine and terephthaloyl chloride on the surface of polyacrylonitrile (PAN) ultrafiltration membranes. ZnO nanoparticles were incorporated in the active separation layer to modify the performances of the membranes. The preparation conditions as the monomer concentration, dosage of nano-ZnO particles and the reaction time on removal of a simulated radioactive nuclide Co (II) were investigated. Fourier transform infrared in attenuated total reflection mode verified the formation of polyamide on the PAN ultraf
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Lee, Young Bok, Gina Chun, Deog J. Kim, et al. "Abstract 1371: Antitumor activity of a new quinoxalinyl-piperazine compound." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-1371.

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Huff, D. W., and P. Murphy. "350. Piperazine: Development and Validation of an Air Monitoring Method." In AIHce 1998. AIHA, 1999. http://dx.doi.org/10.3320/1.2762752.

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Chen, Guan-He, Meng-Hui Li, and Rhoda B. Leron. "Henry’s Law Constant of CO2 in Aqueous Blends of Diethylenetriamine + Piperazine." In Annual International Conference on Chemistry, Chemical Engineering and Chemical Process. Global Science & Technology Forum (GSTF), 2015. http://dx.doi.org/10.5176/2301-3761_ccecp15.30.

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Meyer, P., and B. Czarnecki. "398. 1-(2-Pyridyl) Piperazine Stability on Coated Glass Fiber Filters." In AIHce 1996 - Health Care Industries Papers. AIHA, 1999. http://dx.doi.org/10.3320/1.2765077.

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Reports on the topic "Piperazino"

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Rochelle, Gary, Fred Closmann, Jorge Martorell, et al. Front-End Engineering Design for Piperazine with the Advanced Stripper. Office of Scientific and Technical Information (OSTI), 2022. http://dx.doi.org/10.2172/1878608.

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John T. Cullinane. THERMODYNAMICS AND KINETICS OF AQUEOUS PIPERAZINE WITH POTASSIUM CARBONATE FOR CARBON DIOXIDE ABSORPTION. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/839556.

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Marcus Hilliard. THERMODYNAMICS OF AQUEOUS PIPERAZINE/POTASSIUM CARBONATE/CARBON DIOXIDE CHARACTERIZED BY THE ELECTROLYTE NRTL MODEL WITHIN ASPEN PLUS. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/838130.

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Chen, Eric, Steven Fulk, Matt Beaudry, et al. Evaluation of Concentrated Piperazine for CO2 Capture from Coal-Fired Flue Gas (Final Report, REV0). Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1512446.

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