• Journal of Sensor Science and Technology
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• v.25 no.3
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• pp.218-222
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• 2016

Pure and V-doped NiO porous structures were prepared by the evaporation-induced surfactant assembly and subsequent pyrolysis of assembled structures, and their gas sensing characteristics were investigated. Pure NiO porous structures showed negligible gas responses (S=$R_g/R_a$, $R_g$: sensor resistance in analytic gas; $R_a$: sensor resistance in air) to 5 ppm trimethylamine (S=1.17) as well as other interfering gases such as ethanol, p-xylene, toluene, benzene and formaldehyde (S=1.02-1.13). In contrast, the V-doped NiO porous structures exhibited a high response and selectivity to 5 ppm trimethylamine (S=14.5) with low cross-responses to other interfering gases (S=4.0-8.7) at $350^{\circ}C$. The high gas response of V-doped NiO porous structures to trimethylamine was explained by electronic sensitization, that is, the increase in the chemoresistive variation due to the decrease in the hole concentration. The enhanced selectivity to trimethylamine was discussed in relation to the interaction between basic trimethylamine gas and acidic V catalysts.

• Bulletin of the Korean Chemical Society
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• v.31 no.2
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• pp.483-486
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• 2010

• Biotechnology and Bioprocess Engineering:BBE
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• v.11 no.4
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• pp.337-343
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• 2006

Trimethylamine dehydrogenase (TMADH, EC 1.5.99.7), an iron-sulfur flavoprotein that catalyzes the oxidative demethylation of trimethylamine to form dimethylamine and formaldehyde, was purified from Methylophaga sp. strain SK1. The active TMADH was purified 12.3-fold through three purification steps. The optimal pH and temperature for enzyme activity was determined to be 8.5 and $55^{\circ}C$, respectively. The $V_{max}\;and\;K_m$ values were 7.9 nmol/min/mg protein and 1.5 mM. A genomic DNA of 2,983 bp from Methylophaga sp. strain SK1 was cloned, and DNA sequencing revealed the open reading frame (ORF) of the gene coding for TMADH. The ORF contained 728 amino acids with extensive identity (82%) to that of Methylophilus methylotrophus $W_3A_1$.

• Journal of the Korea Organic Resources Recycling Association
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• v.4 no.2
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• pp.71-75
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• 1996

A bacterium, capable of the degradation of trimethylamine(TMA), dimethylamine, and methylamine, was isolated from an enrichment culture on TMA basal mineral medium. The isolate was identified as Methylobacterium some carbon-carbon bonds compounds like malate, succinate, betaine. When the strain was immobilized to earthworm cast, the biofilter could remove the gaseous TMA of SV $30h^{-1}$, concentration of 120ppm, continuously.

• Journal of Integrative Natural Science
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• v.10 no.4
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• pp.175-191
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• 2017

In organic chemistry amide synthesis is performed through condensation of a carboxylic acid and an amine with releasing one equivalent of water via the corresponding ammonium carboxylate salt. This method is suffering from tedious processes and poor atom-economy due to the adverse thermodynamics of the equilibrium and the high activation barrier for direct coupling of a carboxylic acid and an amine. Most of the chemical approaches to amides formations have been therefore being developed, they are mainly focused on secondary amides. Direct carbonylations of tertiary amines to amides have been an exotic field unresolved, in particular direct carbonylation of trimethylamine in lack of commercial need has been attracted much interests due to the versatile product of N,N-dimethylacetamide in chemical industries and the activation of robust N-C($sp^3$) bond in tertiary amine academically. This review is focused mainly on carbonylation of trimethylamine as one of the typical tertiary amines by transition metals of cobalt, rhodium, platinum, and palladium including the role of methyl iodide as a promoter, the intermediate formation of acyl iodide, the coordination ability of trimethylamine to transition metal catalysts, and any possibility of CO insertion into the bond of Me-N in trimethylamine. In addition reactions of acyl halides as an activated form of acetic acid with amines are reviewed in brief since acyl iodide is suggested as a critical intermediate in those carbonylations of trimethylamine.

• Journal of Integrative Natural Science
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• v.8 no.4
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• pp.235-243
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• 2015

Rhodium(I)-complex of $[Rh(CO)_2I_2{^-}]$ catalyzed carbonylation of anhydrous-trimethylamine in the presence of methyl iodide to give DMAC (N,N-dimethylacetamide) in no solvent. The catalyst had been reused 20 times, the analyses and distillation of collected products showed that the yields of DMAC, MAA (N-methylacetamide), and DMF (N,N-dimethylformamide) were 82.3%, 12.6%, and 4.4%. The conversion rate of trimethylamine was 99 % and the selectivity of DMAC was 82.3% with TON (Turnover Number) of 700. Stepwise procedure of inner-sphere reductive elimination for the formation of DMAC was suggested instead of acyl iodide intermediate.

• Proceedings of the Korea Air Pollution Research Association Conference
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• 2005.11a
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• pp.193-195
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• 2005

• Applied Chemistry for Engineering
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• v.25 no.2
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• pp.167-173
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• 2014

The adsorption characteristics of the pellet-type adsorbent prepared from water treatment sludge for trimethylamine and ammonia were studied. The surface area and pore volume of the pellet-type adsorbent increased during calcination at $500^{\circ}C$. It was confirmed that the adsorbent prepared from water treatment sludge contained Br$\ddot{o}$nsted and Lewis acid sites. The breakthrough time of the adsorbent for both trimethylamine and ammonia was measured at different adsorbent weights and linear velocities while maintaining constant amounts of trimethylamine and ammonia. The kinetic saturation capacity and the adsorption rate constant for trimethylamine and ammonia were determined at different linear velocities by using the Wheeler equation. It was found that the kinetic saturation capacity and the adsorption rate constant were dependent on the linear velocity. An experimental equation could be derived to predict the breakthrough time of the adsorbent prepared from water treatment sludge for trimethylamine and ammonia at different adsorption conditions.

• Journal of the Korean Institute of Gas
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• v.11 no.1 s.34
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• pp.29-33
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• 2007

This study investigates the use of $TiO_{2},\;Pd,\;Pt$, and In which greatly improves a sensitivity to trimethylamine gas. The metal-$SnO_{2}$ thick films were prepared by screen-printing method onto $Al_{2}O_{3}$ substrates with platinum electrode. The sensing characteristics were investigated by measuring the electrical resistance of each sensor in a test box as a function of detecting gas concentration. This was then used to detect trimethylamine, dimethylamine, and ammonia vapours within the concentration range of 100-1000ppm. The gas sensing properties of metal-$SnO_{2}$ mixed thick films depended on the content and variety of metal. It was found that sensitivity and selectivity of the films dopped with 1 wt% Pd and 10 wt% $TiO_{2}$ for trimethylamin gas showed the best result at $250^{\circ}C$.

• Korean Chemical Engineering Research
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• v.54 no.2
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• pp.187-199
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• 2016

In this study CALPUFF modeling was performed to predict a contribution of a separate single point pollutant source as well as of total point pollutant sources of major synthetic fiber manufacturers in Gumi national industrial complex to atmospheric trimethylamine concentration of the same area. In addition, a contribution of the separate single point pollution source to the atmospheric trimethylamine concentration of the same area was estimated relatively to the total point pollutant sources. As a result of the CALPUFF modeling, the maximum atmospheric concentration of trimethylamine in Gumi national industrial complex was appeared upon improving T company emission facility frequently in complex 3 in winter (January) and spring (April) while frequently in complex 1 in summer (July) and autumn (October). Besides, the predicted range of the maximum atmospheric concentration of trimethylamine in complex 1 was improved upon improving its emission facility. However, even though in complex 3 the upper bound of the predicted maximum atmospheric concentrations of trimethylamine was increased upon improving T company emission facility, the predicted value of their second upper bound below the upper bound was very similar to the upper bound of measured atmospheric trimethylamine concentrations in Gumi prior to improving its emission facility. Thus, the effect of improving T company emission facility was estimated huge in complex 1 while it was trivial in complex 3. These maximum concentrations of trimethylamine predicted to estimate the expected contribution of total point pollutant sources by CALPUFF modeling showed the similar values to those measured in the region of Gumi. Therefore, the expected contribution of total point pollutant sources to atmospheric trimethylamine concentration in the area of Gumi was validated.