Relevant bibliographies by topics / Dimethyl Formamide

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

Academic literature on the topic 'Dimethyl Formamide'

Author: Grafiati
Published: 3 June 2025
Last updated: 22 June 2025

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Journal articles on the topic "Dimethyl Formamide"

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T., VEERAIAH, and SONDU S. "Kinetics and Mechanism of Oxidation of Formamide and Dimethyl Formamide by Potassium Bromate in Aqueous Perchloric Acid Medium." Journal of Indian Chemical Society Vol. 74, May 1997 (1997): 402–4. https://doi.org/10.5281/zenodo.5882640.

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Department of Chemistry, University College of Technology. Osmania University, Hyderabad-500 007 <em>Manuscript&nbsp;received 7 July 1995, revised 16 November 1995, accepted 15 February 1996</em> Kinetics and Mechanism of Oxidation of Formamide and Dimethyl Formamide by Potassium Bromate in Aqueous Perchloric Acid Medium
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Baluja, Shipra, Sumitra Chanda, and Kalpen Chavda. "Synthesis, characterization and in vitro antimicrobial activity of cyclic imide: Isoindoline-1, 3-dione derivatives." GSC Biological and Pharmaceutical Sciences 10, no. 1 (2020): 046–58. https://doi.org/10.5281/zenodo.4280907.

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A series of new cyclic imide: isoindoline-1, 3-dione derivatives were synthesized by condensation of 2-hydrazinyl-2-oxo-N-phenylacetamide and phthalic anhydride. The characterization of synthesized compounds was done by IR,&nbsp;<sup>1</sup>H NMR,&nbsp;<sup>13</sup>C NMR and mass spectroscopy. All these synthesized compounds were tested for&nbsp;<em>in vitro</em>&nbsp;antimicrobial against various bacterial and fungal strains in N, N-dimethyl formamide and Dimethyl sulfoxide. It is observed that almost all the compounds showed moderate antimicrobial activity and N, N-dimethyl formamide is better solvent than dimethyl sulfoxide.
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Journal, Baghdad Science. "spectroscopic stury of lewis bases coordinating to vanady." Baghdad Science Journal 3, no. 2 (2006): 344–47. http://dx.doi.org/10.21123/bsj.3.2.344-347.

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Furrer, P., U. Fey, L. Helm, and A. E. Merbach. "Dimethyl formamide exchange on hexakis (dimethyl formamide)-magnesium (II): A1H NMR high-pressure study." High Pressure Research 7, no. 1-6 (1991): 144–46. http://dx.doi.org/10.1080/08957959108245530.

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Futino, DO, MCB Mendes, WNL Matos, RG Mondadori, and CM Lucci. "Glycerol, Methyl-Formamide and Dimethyl-Formamide in Canine Semen Cryopreservation." Reproduction in Domestic Animals 45, no. 2 (2010): 214–20. http://dx.doi.org/10.1111/j.1439-0531.2008.01208.x.

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Guo, Pei Tao. "Improvement in Mechanical Property of SiO2 Films Prepared by Sol-Gel." Advanced Materials Research 744 (August 2013): 269–72. http://dx.doi.org/10.4028/www.scientific.net/amr.744.269.

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Silica films prepared by the base catalyzed sol–gel process show poor mechanical property. In this study, silica anti-reflective films with good mechanical property have been prepared by the catalyzed sol–gel process with dimethyl formamide added as drying control chemical additives. The silica sol was first dip deposited onto substrate to form films on both sides of the substrate and then subjected to thermal treatment. After thermal treatment, the film was achieved due to the formation of porous structure in the resultant film as a result of decomposing tetraethylorthosilicate and dimethyl formamide. Nano-indenter measurement shows that the Young’s modulus and hardness of base catalyzed films are 10-20GPa and 0.25-0.55GPa, respectively. But the films added with dimethyl formamide are much better than those films derived from base-catalyzed silica sols, the Young’s modulus and hardness are 32-39GPa and 1.22-1.47GPa, respectively. The good mechanical properties make such films potential in both military and civil applications.
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Assi. Lect. Hadeel Tareq Hamad , та Dr. Asmaa Satar Jeeiad Mheesin Al-Ragehey. "تأثير قطبية المذيب على خواص التألق لـ) Acriflavine (جزيئي". Journal of the College of Basic Education 21, № 89 (2022): 197. http://dx.doi.org/10.35950/cbej.v21i89.6747.

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تمت دراسة وقياس أطياف الامتصاص والفلورة لمحلول Acriflavine (AF) الذي يذوب في مذيبات [N-N-dimethyl formamide (Dmf) وثنائي ميثيل سلفوكسيد (Dmso) والماء] كدالة للتركيز والمذيب عند طول موجة الإثارة (λex = 414 نانومتر). تم حساب قمم أطياف التألق لمحلول Acriflavine (AF) المذاب في N-N-dimethyl formamide (Dmf) و dimethyl sulphoxide (Dmso) بتركيز (1x10-5M) ، ووجد أنه يساوي (λmax = 497) ، ( λmax = 501) و (λmax = 505) على التوالي. كما تم حساب انزياح قيمة هذه القمم التي تساوي (1292.5) و (1316.5) و (2469.7) على التوالي. حيث نلاحظ أن (stokes shift) ذروة تحول أطياف التألق نحو الطول الموجي الأطول (الانزياح الأحمر) يزداد مع زيادة قطبية المذيب. تؤدي زيادة قطبية المذيبات إلى انخفاض شدة أطياف التألق. كانت جميع القياسات في درجة حرارة الغرفة.
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Mishra, Subhajit, Sougata Santra, and Alakananda Hajra. "Ligand-free reusable nano copper oxide-catalyzed synthesis of 3-amino-1,4-diynes." RSC Advances 5, no. 111 (2015): 91326–29. http://dx.doi.org/10.1039/c5ra18350b.

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The synthesis of 3-amino-1,4-diynes has been developed by the two-component coupling of N,N-dimethyl formamide dimethyl acetal with terminal alkynes using CuO nanoparticles as an efficient catalyst under mild reaction conditions.
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Kiss, László, Ferenc Kovács, and Sándor Kunsági-Máté. "Electropolymerization of N,N'-Diphenylguanidine in Non-Aqueous Aprotic Solvents and Alcohols." Periodica Polytechnica Chemical Engineering 65, no. 1 (2020): 139–47. http://dx.doi.org/10.3311/ppch.14959.

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Electrooxidation of N,N’-diphenylguanidine (1,3-diphenylguanidine) was investigated in aprotic (acetonitrile, acetone, dimethyl sulfoxide, dimethyl formamide, propyleneoxide, nitromethane) and alcoholic (methanol, ethanol, 1-propanol, 1-butanol, 1-pentanol, benzyl alcohol) non-aqueous solvents at platinum electrode with cyclic voltammetry. Its concentration was 5 mM in most cases. In acetonitrile and acetone a sharp voltammetric peak appeared around 1 V vs. reference and currents measured in the subsequent scans showed that the electrode fouled quickly. In dimethyl formamide, the anodic peak heights decreased slowly in the subsequent scans but in dimethyl sulfoxide weak deactivation could be observed both in smaller and in higher concentration. In alcohols, continuous deactivation could be also observed during electrooxidation of N,N’-diphenylguanidine. The permeability studies showed that the structure of the formed polymer films varied significantly according to the solvent used for electrodeposition.
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Kiss, László, Péter Szabó, and Sándor Kunsági-Máté. "Comparison between Electrooxidation of 1-Naphthol and 2-Naphthol in Different Non-Aqueous Solvents and Suppression of Layer Growth of Polymers." Surfaces 7, no. 1 (2024): 164–80. http://dx.doi.org/10.3390/surfaces7010011.

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The two naphthol isomers were investigated in different organic solvents by taking cyclic voltammograms, and fouling took place on a platinum electrode surface, except for dimethyl sulfoxide and dimethyl formamide. Studies in allyl alcohol rarely used in electrochemical investigations pointed to the importance of the carbon–carbon double bond as electrode deactivation was remarkably faster compared with its saturated analog solvent. Similarly, the use of the other unsaturated solvent mesityl oxide in the electropolymerization of naphthols resulted in different findings compared with methyl isobutyl ketone. As dimethyl formamide was the best choice concerning the solubility of products, it was successfully tested in electrode renewal after deactivation in an aqueous solution. The increase in dimethyl formamide content led to more and more improved reproducibility of the currents of the outlined aromatic compounds. Naphthol isomers were assessed in the suppression of layer growth originating from the electrooxidation of another monomer phloroglucinol. Its simultaneous electrooxidation with naphthol monomers had a dramatic effect on layer morphology and it was found that instead of a coherent organic layer originating from the homopolymerization of phloroglucinol, the copolymerization with naphthols led to the development of more porous and rougher deposits. The suppressed electropolymerization thus increased sensitivity towards a chosen redox active compound, 4-methoxyphenol.
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Dissertations / Theses on the topic "Dimethyl Formamide"

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Futino, Daniele Oga. "Uso do glicerol, metil-formamida e dimetil-formamida como crioprotetores do sêmen canino." reponame:Repositório Institucional da UnB, 2008. http://repositorio.unb.br/handle/10482/1746.

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Dissertação (mestrado)—Universidade de Brasília, Faculdade de Agronomia e Medicina Veterinária, 2008.<br>Submitted by Diogo Trindade Fóis (diogo_fois@hotmail.com) on 2009-09-08T16:56:50Z No. of bitstreams: 1 2008_DanieleOgaFutino.pdf: 344538 bytes, checksum: d57e476051f680fd9bf2ae927cc6d356 (MD5)<br>Approved for entry into archive by Tania Milca Carvalho Malheiros(tania@bce.unb.br) on 2009-09-22T16:00:36Z (GMT) No. of bitstreams: 1 2008_DanieleOgaFutino.pdf: 344538 bytes, checksum: d57e476051f680fd9bf2ae927cc6d356 (MD5)<br>Made available in DSpace on 2009-09-22T16:00:37Z (GMT). No. of bitstreams: 1 2008_DanieleOgaFutino.pdf: 344538 bytes, checksum: d57e476051f680fd9bf2ae927cc6d356 (MD5) Previous issue date: 2008-05<br>A crescente demanda por biotécnicas reprodutivas em cães tem despertado grande interesse no desenvolvimento de protocolos de congelação de sêmen canino que, associados à correta identificação do momento ótimo para a inseminação, resultem em taxas de fertilidade próximas às da inseminação artificial com sêmen fresco ou resfriado. A grande vantagem da congelação do sêmen é a sua viabilidade por tempo indeterminado. O crioprotetor de eleição na congelação do sêmen canino é o glicerol, entretanto a busca por crioprotetores alternativos tem sido crescente. O presente trabalho objetivou comparar a eficiência da metil-formamida (MF) e da dimetil-formamida (DF) em relação ao glicerol (GL) como crioprotetores na congelação do sêmen canino. Para o experimento, foram utilizados pools de amostras de sêmen de cinco cães da Polícia Federal, coletadas por manipulação digital. Cada pool foi fracionado em três amostras, sendo cada uma delas submetida a um dos três crioprotetores, sempre à concentração final de 3% em diluidor Tris-gema. Cada tratamento foi repetido cinco vezes. O sêmen foi avaliado subjetivamente quanto à motilidade total e progressiva, vigor e morfologia logo após a coleta do sêmen, formação do pool, diluição, resfriamento e descongelação. As alíquotas foram resfriadas e equilibradas a 4°C por uma hora e meia e envasadas em palhetas de 0,5m?. Em seguida, procedeu-se a congelação, expondo-se as palhetas ao vapor de nitrogênio líquido por 15 minutos seguido de imersão e armazenamento no nitrogênio líquido. As palhetas foram acondicionadas em botijão criogênico por um período mínimo de sete dias antes da descongelação. A descongelação foi feita em banho-maria a 37°C durante um minuto, permanecendo a esta temperatura durante 30 minutos para a realização do teste hiposmótico (HOST). A longevidade espermática foi feita realizando-se o teste de termorresistência (TTR). A análise estatística foi realizada utilizando-se análises de variância (ANOVA) e teste PLSD de Fischer. As amostras de sêmen fresco apresentaram características físicas e morfológicas dentro da normalidade (93,60±7,60%, 90,40±8,70%, 4,8±0,44 e 90,25±3,17% para motilidade total, motilidade progressiva, vigor e morfologia normal, respectivamente). Após a descongelação, foram observadas diferenças significativas (P<0,05) entre GL e DF em relação à motilidade total e progressiva e vigor. Em relação à MF, não houve diferenças significativas em relação ao GL ou à DF em nenhum parâmetro avaliado. As médias para motilidade total, motilidade progressiva, vigor e morfologia normal na pós-descongelação foram 69,00±5,47%, 61,00±7,41%, 2,9±0,54% e 57,10±5,01% para o GL, 59,00±8,94%, 50,00±10,00%, 2,5±0,70 e 66,90±7,74% para a MF e 44,00±21,03%, 37,00±19,87%, 2,1±0,65 e 61,10±5,59% para a DF, respectivamente. No teste HOST o GL apresentou-se superior à MF e DF (57,80±12,47%, 35,80±18,47% e 34,40±9,40%, porcentagens médias de células com membranas íntegras para GL, MF e DF, respectivamente). Durante o TRT, não houve diferenças entre o GL e a MF e ambos mostraram-se superior à DF. De acordo com os resultados encontrados, pode-se concluir que a MF apresenta resultados semelhantes ao GL, e, portanto pode ser considerada uma alternativa como crioprotetor na criopreservação de sêmen canino. Testes comparando diferentes concentrações da MF são necessários visando seu melhor desempenho como crioprotetor. __________________________________________________________________________________________ ABSTRACT<br>Due to an increasing demand for canine reproductive biotechnologies, it has been crescent interests for improving freezing protocols employed for canine semen which, associated to a correct identification of optimal breeding time, results on fertility rates close to those achieved with artificial insemination with fresh or cooled semen. The unlimited viability of cryopreserved semen is the greatest advantage of this technique. Glycerol is the most commonly used cryoprotectant for dog sperm however the search for alternative cryoprotectants has increased. The aim of the present work was to compare the efficiency of methyl-formamide (MF), dimethyl-formamide (DF) and glycerol (GL) as cryoprotectants in canine semen cryopreservation. Five dogs were used in the experiment. Ejaculates were collected, pooled and divided into three aliquots and each one was submitted to one of the three cryoprotectants, with final concentration of 3% in egg yolk-TRIS extender. Treatments were repeated five times. Semen was subjectively evaluated for total and progressive motility, vigor and morphology immediately after each of the following procedures: semen collection, pool formation, dilution, chilling and freezing/thawing. Sperm membrane functional integrity was assessed by hypo-osmotic swelling test (HOST), ans longevity was assessed using the thermoresistance test (TRT). Fresh semen showed normal physical and morphological characteristics. After thawing, differences were observed between semen frozen using GL and DF regarding total and progressive motility and bigot (P<0.05) but not between MF and GL or MF and DF. Means for total motility, progressive motility, vigor and morphologically normal spermatozoa were respectively 69,00±5,47%, 61,00±7,41%, 2,9±0,54% e 57,10±5,01% for GL, 59,00±8,94%, 50,00±10,00%, 2,5±0,7 and 66,90±7,7% for MF and 4,00±21,03%, 37,00±19,87%, 2,1±0,65 and 61,10±5,59% for DF. On HOST, GL was superior to MF and DF (57,80±12,47%, 35,80±18,47% and 34,40±9,40%, respectively). During TRT, both GL and MF were superior to DF, with no differences between GL and MF. In conclusion, the use of MF as cryoprotectant showed results similar to GL, except on HOST, and can br considered as an alternative in canine semen cryopreservation. Further studies testing different concentrations of MF may improve its effects on cryopreservation of canine semen.
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Osorio, Jair Perez. "Efeito da adição fracionada de Dimetil formamida e das curvas de congelamento na viabilidade in vitro pós-descongelamento do espermatozoide eqüino." Universidade Federal de Minas Gerais, 2006. http://hdl.handle.net/1843/LGPD-6NCFWH.

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The aim of this research was to evaluate the efficiency of three times of fractionate addition of 5%, the dimethyl formamide to the half seminal extender modified base INRA 82, and its interaction with the time of balance and the rates of freezing in the criopreservation of equine spermatozoa. Ejaculates of six stallions was used to test three times of addition of the dimethyl formamide; Time 1: addition of the tenth part of dimethyl formamide to each the one minute in the time of ten minutes; Time 2: addition of the tenth part of dimethyl formamide to each the two minutes in the time of twenty minutes; Time 3: addition of the tenth part of dimethyl formamide to each the three minutes in the time of thirty minutes. Completing the average period of one hour and eight minutes in ambient temperature since the beginning until addition of the crioprotectan all the samples had been cooled until 5°C using one scheme computerized to a rates of cooling 0,25°C/min. 3 different procedures for the freezing had been tested: a) without time of additional balance 5°C and freezing 4cm above of the nitrogen level fifteen minutes, and posterior submersion of the samples in nitrogen liquid; b) with time of additional balance 5°C of forty five minutes and freezing 4cm above of the nitrogen level fifteen minutes, and posterior submersion of the samples in nitrogen liquid e; c) with time of additional balance 5°C of forty five minutes and freezing computerized to one rates of -10°C/min ties -127°C per fifteen minutes, and posterior submersion of the samples in nitrogen liquid. The thawing was made 52°C per ten seconds, followed of immersion in bath-Maria 37°C per thirty seconds. Immediately post thaw the parameters of total motility, motility progressive and spermatic vigor were evaluated under microscopy 400X. The integrity of the plasmatic membrane of the tail was evaluated through the hiposmotic swelling test and the functional and structural sperm membrane integrity were evaluate by the fluorescent dyes, carboxyfluorescein diacetate and propidium iodide respectively. The spermatozoa were also evaluated in the temperature resistance. Was not observed significant difference (P> 0, 05) enters the three times of addition and enters the freezing rates. The results allow concluding that the changes of the time of addition of the crioprotectan of fractionate form and the curve of freezing did not modify the equine spermatic viability evaluated in vitro..<br>Este trabalho teve como objetivo avaliar a eficiência de três tempos de adição fracionada de 5%, da dimetil formamida (DMF) ao meio diluídor base INRA 82 modificado, a sua interação com o tempo de equilíbrio e a curva de congelamento na criopreservação de espermatozóides eqüinos. Um ejaculado de seis garanhões foi utilizado para testar três tempos de adição da dimetil formamida: Tempo 1: adição da décima parte da dimetil formamida a cada minuto no tempo de dez minutos; Tempo 2: adição da décima parte da dimetil formamida à cada dois minutos no tempo de vinte minutos; Tempo 3: adição da décima parte da dimetil formamida a cada três minutos no tempo de trinta minutos. Completando-se o período médio de uma hora e oito minutos em temperatura ambiente desde o início até a adição do crioprotetor todas as amostras foram resfriadas até 5°C utilizando uma máquina computadorizada a uma taxa de 0,25°C/min. Foram testadas três diferentes procedimentos para o congelamento: a) sem tempo de equilíbrio adicional à 5°C e congelamento 4cm acima do nível de nitrogênio líquido por quinze minutos, e posterior submersão das amostras no nitrogênio líquido; b) com tempo de equilíbrio adicional a 5°C de quarenta e cinco minutos e congelamento 4cm acima do nível de nitrogênio líquido por quinze minutos, e posterior submersão das amostras no nitrogênio liquido; c) com tempo de equilíbrio adicional à 5°C de quarenta e cinco minutos e congelamento computadorizado a uma taxa de -10°C/min ate -127°C por quinze minutos, e posterior submersão das amostras no nitrogênio liquido. O descongelamento foi feito a 52°C por dez segundos, seguidos de imersão em banhomaria a 37°C por trinta segundos. Após o descongelamento foram avaliados os parâmetros de motilidade total, motilidade progressiva e vigor espermático em microscopia óptica, com aumento de 400X. A integridade da membrana plasmática da cauda e da cabeça foi avaliada pelo teste hiposmótico e pela coloração de fluorescência respectivamente. Os espermatozóides foram submetidos ao teste de termoresistência. Não foi observada diferença significativa (P> 0,05) entre os três tempos de adição nem as curvas de congelamento. Os resultados permitem concluir que a mudança do tempo de adição do crioprotetor de forma fracionada e da curva de congelamento não altera a viabilidade espermática eqüina avaliada in vitro.
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Dorairaj, S. "A nucleate pool boiling study of refrigerant-22 - dimethyl formamide mixtures." Thesis, 1986. http://localhost:8080/iit/handle/2074/4915.

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ZHANG, YU-HUA, and 張毓華. "Study on treatment of volatile organic compounds (VOCs) by catalytic incineration: Dimethyl formamide (DMF)." Thesis, 1992. http://ndltd.ncl.edu.tw/handle/00807882624062695113.

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Mazzini, Virginia. "Specific ion effects in non-aqueous solutions." Phd thesis, 2017. http://hdl.handle.net/1885/144595.

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Electrolyte solutions play a central role in life and technological processes because of their complexity. This complexity is yet to be described by a predictive theory of the specific effects that different ions induce in solution. The vast majority of investigations of specific-ion effects have been conducted in aqueous solutions. These studies have revealed that amongst the complexity, the effectiveness of the ions often follow trends that are apparent across a number of very different experiments, revealing an underlying order (e.g. the Hofmeister series). It is often assumed that water itself is intricately involved in these trends. Here I investigate specific-ion effects in non-aqueous solvents rather than water. By extending the investigation to a number of non-aqueous solvents, the role of the solvent in specific-ion effect trends can be elucidated and a better understanding of the general phenomenon gained. Firstly, a more definite terminology is developed for describing the specific-ion effects trends in order to address the current confusion in the literature and provide a basis for the following investigations. An extensive investigation of the scarce literature demonstrates that water is by no means a special solvent with regards to ion-specificity, and that within the complexity there is universality. An investigation of electrostriction under the conditions of infinite dilution shows that the same fundamental specific ion trends are observed across all solvents, demonstrating that ion-specificity arises from the ions themselves. In this regard the influence of solvents, surfaces and real concentrations of electrolytes can be seen as perturbations to this fundamental series. Further work shows that for systems that are perturbed, the trends in non-aqueous protic solvents can be expected to follow the same trend in water; and in aprotic solvents the cations are more likely to adhere to the trend in water than the anions. My experimental work focuses on specific-anion effects of seven Hofmeister sodium salts in the solvents: water, methanol, formamide, dimethyl sulfoxide and propylene carbonate. Two very different experiments were performed; the elution of electrolytes from a size-exclusion chromatography column and an investigation of the electrolyte moderated swelling of a cationic brush (PMETAC) using a Quartz Crystal Microbalance (QCM). The trends observed are consistent across these experiments. A forward or reverse Hofmeister series is observed in practically all salt-solvent combinations, and the reversal is attributed to the polarisability of the solvent. Finally, a qualitative model of ion specific trends is formulated, where the specific-ion effects are fundamentally a property of the ion, and the associated trends correspond to the Hofmeister series for anions and the lyotropic series for cations. When the concentration is increased, or surfaces introduced, the effects of ion-ion interactions and ion-surface interactions can perturb the fundamental series. The perturbation of the series is related to the proticity of the solvent for ion-ion interactions, whereas the polarisability of the solvent and ion are important when a surface is present. This work for the first time individuates the principal properties of the solvent that affect their ordering: proticity and polarisability.
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Books on the topic "Dimethyl Formamide"

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National Register of Foreign Collaborations (India) and India. Dept. of Scientific & Industrial Research., eds. Technology in Indian dimethyl formamide industry: A status report prepared under the National Register of Foreign Collaborations. Govt. of India, Dept. of Scientific & Industrial Research, Ministry of Science and Technology, 1993.

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Book chapters on the topic "Dimethyl Formamide"

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Winkelmann, Jochen. "Diffusion coefficient of N,N-dimethyl-formamide in N,N-dimethyl-formamide-d7 at infinite dilution." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_1492.

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Winkelmann, Jochen. "Self-diffusion coefficient of N,N-dimethyl-formamide." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_84.

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Winkelmann, J. "Diffusion of propene (1); N,N-dimethyl-formamide (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1497.

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Winkelmann, J. "Diffusion of xenon (1); N,N-dimethyl-formamide (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1651.

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Winkelmann, J. "Diffusion of N,N-dimethyl-formamide (1); air (2)." In Gases in Gases, Liquids and their Mixtures. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_658.

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Winkelmann, Jochen. "Diffusion coefficient of ferrocene in N,N-dimethyl-formamide." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_711.

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Winkelmann, Jochen. "Self-diffusion coefficient of N,N-dimethyl-formamide-d7." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_73.

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Winkelmann, Jochen. "Diffusion coefficient of water in N,N-dimethyl-formamide." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_1239.

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Winkelmann, Jochen. "Diffusion coefficient of acetonitrile in N,N-dimethyl-formamide." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_133.

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Winkelmann, Jochen. "Diffusion coefficient of N,N-dimethyl-formamide in methanol." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_232.

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Conference papers on the topic "Dimethyl Formamide"

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Fran, Yui-Shin, Tsung-Yuan Tseng, and Wen-Feng Hsieh. "Investigation of Er-doped glasses by two-step hydrolysis with N,N-dimethyl formamide." In SPIE's 1994 International Symposium on Optics, Imaging, and Instrumentation, edited by John D. Mackenzie. SPIE, 1994. http://dx.doi.org/10.1117/12.189002.

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Khandelwal, Vrushabh Manoj, Prabhakar Bhawagtrao Undre, Faiza Awad Saif, et al. "Investigation of intermolecular interactions between formamide-dimethyl amino ethanol binary mixtures through dielectric relaxation and FTIR study." In PROCEEDINGS OF THE INTERNATIONAL CONFERENCE ON PHYSICS OF MATERIALS AND NANOTECHNOLOGY ICPN 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0009071.

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Guo, Pei-Tao, Yu-Hong Man, and Yong-Ping Zhang. "Effects of Dimethyl Formamide on Laser-induced Damage to SiO2 Films Prepared by the Sol-gel Method." In 2015 International Conference on Material Science and Applications (icmsa-15). Atlantis Press, 2015. http://dx.doi.org/10.2991/icmsa-15.2015.59.

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Raghavan, S. Sethu, and Raj M. Manglik. "Visualization of Micro-Scale Bubble Dynamics in Pure Liquids and Aqueous Surfactant Solutions." In ASME 2004 Heat Transfer/Fluids Engineering Summer Conference. ASMEDC, 2004. http://dx.doi.org/10.1115/ht-fed2004-56858.

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Abstract:
Growth and departure of a single adiabatic bubble in pure liquids and aqueous surfactant solutions is visualized. High-resolution photographic records are obtained that characterize the micro-scale bubble dynamics (shape, size, and post-departure translation), the mean bubble diameter at different time periods of its growth and departure, and the bubble surface age (the time interval from the newly formed interface to the attainment of departure diameter). This pre- and post-departure dynamics of air bubbles is visualized in water, N, N dimethyl-formamide (DMF), and ethyl alcohol (all pure liquids), and aqueous surfactant solutions of SDS (1250 wppm, 2500 wppm, and 5000 wppm), CTAB (200 wppm), and Triton X-305 (1000 wppm). The evolution of different bubble shapes, sizes, and departure frequencies is presented to highlight the effects of surface-active forces. In the case of surfactant solutions, the dynamic effects of the molecular-scale adsorption-desorption dynamics of the additive at the liquid-air interface that manifests in the dynamic surface tension is also delineated.
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