Добірка наукової літератури з теми "Triethylamine (TMA)"

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Статті в журналах з теми "Triethylamine (TMA)"

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Suzuki, S., T. Doke, A. Hitachi, A. Yunoki, K. Masuda, and T. Takahashi. "Photoionization effect in liquid xenon doped with triethylamine (TEA) or trimethylamine (TMA)." Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 245, no. 1 (April 1986): 78–81. http://dx.doi.org/10.1016/0168-9002(86)90260-3.

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Tzitzikalaki, Evangelia, Nikos Kalivitis, and Maria Kanakidou. "Observations of Gas-Phase Alkylamines at a Coastal Site in the East Mediterranean Atmosphere." Atmosphere 12, no. 11 (November 3, 2021): 1454. http://dx.doi.org/10.3390/atmos12111454.

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Atmospheric amines are ubiquitous compounds in the atmosphere, having both natural and anthropogenic origin. Recently, they have been identified as important contributors to new particle formation in the atmosphere, but observations of their atmospheric concentrations are scarce. In the present study we introduce the first systematic long-term observations of gas-phase amines measurements in the East Mediterranean atmosphere. Air samples were collected at the Finokalia monitoring station of the University of Crete during a 3.5-year period from January 2013 to July 2016, and analyzed after extraction using a high-performance liquid chromatography triple quadrupole mass spectrometer. The detected alkylamines were the sum of dimethylamine and ethylamine (DMA+EA), trimethylamine (TMA), diethylamine (DEA) and triethylamine (TEA). DMA+EA and TMA were the most abundant alkylamines, with concentrations spanning from the detection limit to 78.0 and 69.8 pptv, and average concentrations of 7.8 ± 12.1 and 7.5 ± 12.4 pptv, respectively. Amines showed pronounced seasonal variability with DMA+EA and TMA concentrations being higher in winter. Statistical analysis of the observations showed different sources for each of the studied amines, except for DMA+ΕA and DEA that appear to have common sources in the region. This analysis points to a marine source of TMA and animal husbandry in the area as a potential source of TEA. None of the alkylamines is correlated with other anthropogenic sources. Furthermore, no clear association was found between the seasonality of NPF events and alkylamines concentrations, while a clear correlation was detected between the seasonality of nucleation mode particle (dp < 25 nm) number concentrations and alkylamine concentrations, indicating that amines may contribute to nucleation mode particles’ production.
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Yoo, Ran, Hyun-Sook Lee, Wonkyung Kim, Yunji Park, Aran Koo, Sang-Hyun Jin, Thang Viet Pham, Myung Jong Kim, Sunglyul Maeng, and Wooyoung Lee. "Selective Detection of Nitrogen-Containing Compound Gases." Sensors 19, no. 16 (August 15, 2019): 3565. http://dx.doi.org/10.3390/s19163565.

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N-containing gaseous compounds, such as trimethylamine (TMA), triethylamine (TEA), ammonia (NH3), nitrogen monoxide (NO), and nitrogen dioxide (NO2) exude irritating odors and are harmful to the human respiratory system at high concentrations. In this study, we investigated the sensing responses of five sensor materials—Al-doped ZnO (AZO) nanoparticles (NPs), Pt-loaded AZO NPs, a Pt-loaded WO3 (Pt-WO3) thin film, an Au-loaded WO3 (Au-WO3) thin film, and N-doped graphene—to the five aforementioned gases at a concentration of 10 parts per million (ppm). The ZnO- and WO3-based materials exhibited n-type semiconducting behavior, and their responses to tertiary amines were significantly higher than those of nitric oxides. The N-doped graphene exhibited p-type semiconducting behavior and responded only to nitric oxides. The Au- and Pt-WO3 thin films exhibited extremely high responses of approximately 100,000 for 10 ppm of triethylamine (TEA) and approximately −2700 for 10 ppm of NO2, respectively. These sensing responses are superior to those of previously reported sensors based on semiconducting metal oxides. On the basis of the sensing response results, we drew radar plots, which indicated that selective pattern recognition could be achieved by using the five sensing materials together. Thus, we demonstrated the possibility to distinguish each type of gas by applying the patterns to recognition techniques.
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VandenBoer, T. C., A. Petroff, M. Z. Markovic, and J. G. Murphy. "Size distribution of alkyl amines in continental particulate matter and their online detection in the gas and particle phase." Atmospheric Chemistry and Physics Discussions 10, no. 11 (November 11, 2010): 27435–77. http://dx.doi.org/10.5194/acpd-10-27435-2010.

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Abstract. An ion chromatographic method is described for the quantification of the simple alkyl amines: methylamine (MA), dimethylamine (DMA), trimethylamine (TMA), ethylamine (EA), diethylamine (DEA) and triethylamine (TEA), in the ambient atmosphere. Limits of detection (3σ) are in the tens of pmol range for all of these amines, and good resolution is achieved for all compounds except for TMA and DEA. The technique was applied to the analysis of time-integrated samples collected using a micro-orifice uniform deposition impactor (MOUDI) with ten stages for size resolution of particles with aerodynamic diameters between 56 nm and 18 μm. In eight samples from urban and rural continental airmasses, the mass loading of amines consistently maximized on the stage corresponding to particles with aerodynamic diameters between 320 and 560 nm. The molar ratio of amines to ammonium (R3NH+/NH4+) in fine aerosol ranged between 0.005 and 0.2, and maximized for the smallest particle sizes. The size-dependence of the R3NH+/NH4+ ratio indicates differences in the relative importance of the processes leading to the incorporation of amines and ammonia into secondary particles. The technique was also used to make simultaneous hourly online measurements of amines in the gas phase and in fine particulate matter using an Ambient Ion Monitor Ion Chromatograph (AIM-IC). During a ten day campaign in downtown Toronto, DMA, TMA+DEA, and TEA were observed to range from below detection limit to 2.7 ppt in the gas phase. In the particle phase, MAH+ and TMAH++DEAH+ were observed to range from below detection limit up to 15 ng m−3. The presence of detectable levels of amines in the particle phase corresponded to periods with higher relative humidity and higher mass loadings of nitrate. While the hourly measurements made using the AIM-IC provide data that can be used the evaluate the application of gas-particle partitioning models to amines, the strong size-dependence of the R3NH+/NH4+ ratio indicates that using bulk measurements and an assumption of internal mixing may not be appropriate.
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VandenBoer, T. C., A. Petroff, M. Z. Markovic, and J. G. Murphy. "Size distribution of alkyl amines in continental particulate matter and their online detection in the gas and particle phase." Atmospheric Chemistry and Physics 11, no. 9 (May 10, 2011): 4319–32. http://dx.doi.org/10.5194/acp-11-4319-2011.

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Abstract. An ion chromatographic method is described for the quantification of the simple alkyl amines: methylamine (MA), dimethylamine (DMA), trimethylamine (TMA), ethylamine (EA), diethylamine (DEA) and triethylamine (TEA), in the ambient atmosphere. Limits of detection (3σ) are in the tens of pmol range for all of these amines, and good resolution is achieved for all compounds except for TMA and DEA. The technique was applied to the analysis of time-integrated samples collected using a micro-orifice uniform deposition impactor (MOUDI) with ten stages for size resolution of particles with aerodynamic diameters between 56 nm and 18 μm. In eight samples from urban and rural continental airmasses, the mass loading of amines consistently maximized on the stage corresponding to particles with aerodynamic diameters between 320 and 560 nm. The molar ratio of amines to ammonium (R3NH+/NH4+) in fine aerosol ranged between 0.005 and 0.2, and maximized for the smallest particle sizes. The size-dependence of the R3NH+/NH4+ ratio indicates differences in the relative importance of the processes leading to the incorporation of amines and ammonia into secondary particles. The technique was also used to make simultaneous hourly online measurements of amines in the gas phase and in fine particulate matter using an Ambient Ion Monitor Ion Chromatograph (AIM-IC). During a ten day campaign in downtown Toronto, DMA, TMA + DEA, and TEA were observed to range from below detection limit to 2.7 ppt in the gas phase. In the particle phase, MAH+ and TMAH+ + DEAH+ were observed to range from below detection limit up to 15 ng m−3. The presence of detectable levels of amines in the particle phase corresponded to periods with higher relative humidity and higher mass loadings of nitrate. While the hourly measurements made using the AIM-IC provide data that can be used to evaluate the application of gas-particle partitioning models to amines, the strong size-dependence of the R3NH+/NH4+ ratio indicates that using bulk measurements may not be appropriate.
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Szulczyński, Bartosz, and Jacek Gębicki. "Electronic nose – an instrument for odour nuisances monitoring." E3S Web of Conferences 100 (2019): 00079. http://dx.doi.org/10.1051/e3sconf/201910000079.

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An increasingly frequent problem of people living in urban agglomerations is the occurrence of odour nuisance. Although the source of these nuisances is different, their common feature is that they are a complex mixture of odour compounds with different odour thresholds. However, from a practical point of view, the most valuable would be a direct link between the odour intensity and the results of on-line analytical air monitoring. Such a possibility is created by the use of electronic noses (devices that are supposed to imitate the human sense of smell) to measure odours. The paper presents the use of an electronic nose combined with multiple liear regression model (MLR) to determine the odour intensity of the two-component mixture samples of commonly known odour compounds: trimethylamine (TMA) and triethylamine (TEA) in concentration range 50–200 ppm v/v. The obtained results were compared with the theoretical values determined using Zwaardemaker and euclidean additivity (EA) models. For high concentrations of substances in the mixtures (> 150 ppm v/v), the masking effect was observed.
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Carbone, Alessandra, Rolando Pedicini, Irene Gatto, Ada Saccà, Assunta Patti, Giovanni Bella, and Massimiliano Cordaro. "Development of Polymeric Membranes Based on Quaternized Polysulfones for AMFC Applications." Polymers 12, no. 2 (February 1, 2020): 283. http://dx.doi.org/10.3390/polym12020283.

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A series of quaternary ammonium-functionalized polysulfones were successfully synthesized using a chloromethylation two-step method. In particular, triethylammonium and trimethylammonium polysulfone derivatives with different functionalization degrees from 60% to 150% were investigated. NMR spectroscopic techniques were used to determine the degree of functionalization of the polymers. The possibility to predict the functionalization degree by a reaction tool based on a linear regression was highlighted. Anionic membranes with a good homogeneity of thickness were prepared using a doctor-blade casting method of functionalized polymers. The chemical–physical data showed that ion exchange capacity, water content, and wettability increase with the increase of functionalization degree. A higher wettability was found for membranes prepared by the trimethylamine (TMA) quaternary ammonium group. A degree of functionalization of 100% was chosen for an electrochemical test as the best compromise between chemical–physical properties and mechanical stability. From anionic conductivity measurement a better stability was found for the triethylamine (TEA)-based membrane due to a lower swelling effect. A power density of about 300 mW/cm2 for the TEA-based sample at 60 °C in a H2/O2 fuel cell was found.
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Citraningrum, H. M., and Jhy-Chern Liu. "Effect of competing amines on the removal of tetramethylammonium hydroxide from solution using ion exchange." Water Science and Technology 74, no. 2 (May 10, 2016): 466–72. http://dx.doi.org/10.2166/wst.2016.167.

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Tetramethylammonium hydroxide (TMAH, TMA+) has been widely used as the photoresist developer in semiconductor and thin film transistor liquid crystal display manufacturing. In this study, TMAH-containing wastewater was treated by ion exchange method. Strong acid cation exchange resin was used. A kinetics study revealed that the ion exchange reaction reached equilibrium within 20 min and it could be described by a pseudo-second-order model. To assess the effects of competing ions, wastewater was spiked with three different amines, namely ethylamine (EA+), diethylamine (DEA+), and triethylamine (TEA+). TMAH uptake decreased when in the presence of amines, and it decreased in the order EA+ &lt; DEA+ &lt; TEA+. It could be attributed to different proton affinity (PA) and the strength of affinity between amine molecules and resin matrix, as found from the ab initio calculation values and Langmuir isotherm parameters. However, the interaction energy between sulphonic acid groups and interfering amines in solution using density functional theory (DFT) calculation resulted in a different trend compared with that of PA. The difference might be caused by stabilization of amines by resin matrix and different molecular structures.
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Nordin, N. A. H. M., A. F. Ismail, A. Mustafa, P. S. Goh, D. Rana, and T. Matsuura. "Aqueous room temperature synthesis of zeolitic imidazole framework 8 (ZIF-8) with various concentrations of triethylamine." RSC Adv. 4, no. 63 (2014): 33292–300. http://dx.doi.org/10.1039/c4ra03593c.

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Kajimoto, Shinji, Nak-Hyun Seong, Hiroshi Fukumura, and Dana D. Dlott. "Picosecond dynamics of hydrogen bond rearrangements during phase separation of a triethylamine and water mixture." Photochem. Photobiol. Sci. 13, no. 6 (2014): 891–97. http://dx.doi.org/10.1039/c4pp00048j.

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A picosecond temperature jump experiment reveals that phase separation in a liquid triethylamine (TEA)–water mixture started from hydrogen bond scission of TEA–water aggregates in TEA-rich regions and then in water-rich regions.
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Дисертації з теми "Triethylamine (TMA)"

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Ceppa, Florencia Andrea. "Diet:microbiota interaction in the gut focus on amino acid metabolism." Doctoral thesis, 2016. http://hdl.handle.net/10449/33118.

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This study aims to measure the impact of protein and amino acid fermentation on the composition and metabolic output of gut microbiota. Although dissimilatory pathways have been described for most amino acids, microbial degradation routes within the gut microbiota are relatively unexplored. The objectives were (1) to characterize amino acid breakdown by the colonic microbiota, (2) to determine the fermentation products formed from individual amino acids/protein (3) to examine how amino acid metabolism is impacted by the presence of a fermentable fiber (prebiotic inulin) and finally (4) to evaluate with an in vivo model (trout fish) diet:- microbe interactions and the development of gut microbiota during fish farming. Interactions between the healthy human intestinal microbiota of the distal colon and different combinations of nutrients were simulated using in vitro pH-controlled anaerobic batch cultures of human faeces. Combining high-throughput sequencing of 16S rRNA amplicons, with high-throughput 1 H NMR, changes in faecal microbiota composition and metabolic output were measured. During exogenous substrate microbial fermentation (e.g. beef, Trp or fish feed) in the large bowel bioactive compounds (harmful or beneficial) are produced. Many factors affect the gut-microbial metabolism including pH, type and quantity of growth substrate (e.g. protein/carbohydrate) and make up of the gut microbiota. Considerable interindividual variation was observed in response to different digested substrates but over all, the beneficial impact of prebiotic fiber fermentation on production of bioactive compounds from amino acids/proteins was confirmed in this study. In trout, although our dietary intervention with essential oils had little impact on the gut microbiota, the study showed for the first time a dramatic shift in the composition and diversity of the gut microbiota in juvenile compared to adult fish. These observations may have relevance in designing dietary strategies to reduce chronic diseases like colon cancer and heart disease and for fish farming respectively
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Тези доповідей конференцій з теми "Triethylamine (TMA)"

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Chen, Hao, Min Xu, Gaoming Zhang, Ming Zhang, and Yuyin Zhang. "Investigation of Ethanol Spray From Different DI Injectors by Using Two-Dimensional Laser Induced Exciplex Fluorescence at Potential Cold-Start Condition." In ASME 2010 Internal Combustion Engine Division Fall Technical Conference. ASMEDC, 2010. http://dx.doi.org/10.1115/icef2010-35090.

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The spray evaporation of gasoline and ethanol fuel was investigated qualitatively through the use of the planar laser induced exciplex fluorescence (PLIEF) technique in a constant volume chamber. The effect of fuel temperature and ambient pressure on spray evaporation was identified over a range of conditions. Both a swirl injector and a multi-hole injector were examined for each of the two fuels. A coevaporative mixture of benzene and triethylamine (TEA) was used as a fluorescent seeding material to study the evaporation processes of ethanol fuel. A mixture of fluorobenzene (FB) and diethylmethylamine (DEMA) in n-hexane, which has been proved to be a suitable seeding material for LIEF measurement, allowed for the investigation of the evaporation processes of gasoline fuel mixture. Remarkable spray evaporation processes were observed for both gasoline and ethanol fuel by increasing fuel temperature or by reducing ambient pressure to a vacuum. Especially after achieving flash-boiling, the vapor distribution of multi-plume spray increases dramatically, and the vapor phase of spray from swirl injector gathers to the centerline of injector by increasing the superheated degree. The collapsing of both liquid and vapor phases of n-hexane is stronger than that of ethanol spray for both swirl and multi-hole injectors.
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Haq, Kautsar Ul, Septi Rosiana Dewi, Sherly Dwi Cicilianingrum, Amalia Muti Anggraini, Zella Dwipuspita Dahana, Indrianti Yunita Sari, Rina Dewi Renjanawati, et al. "Synthesis of 5-benzylidene-hydantoin and 5-benzylidene-creatinine derivatives under mixed catalyst systems of urea-p-toluenesulfonic acid (Urea-PTSA) and guanidine hydrochloride-triethylamine (GnHCl-TEA)." In THE 14TH JOINT CONFERENCE ON CHEMISTRY 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0005378.

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