• Korean Journal of Food Science and Technology
• /
• v.6 no.1
• /
• pp.6-11
• /
• 1974

Four new compounds; 2,2'-methylene-bis [3, 4, 6-trichloro ${{\beta}-(o-nitroanilino)$ propionoxy} benzene]; m.p. $200{\sim}202^{\circ}C,\;C_{31}H_{22}O_8N_4Cl_6$ 2,2'-methylene-bis [3, 4, 6-trichloro ${{\beta}-(p-nitroanilino)$ propionoxy} benzene]; m.p. $168-170^{\circ}C,\;C_{31}H_{22}O_8N_4Cl_6$ : 2,2'-Methylene-bis [3, 4, 6-trichloro ${{\beta}-(o-chloro-p-nitroanilino)$ propionoxy} benzene]; m.p. $170.5-172.5^{\circ}C,\;C_{31}H_{20}O_8N_4Cl_8$ : 2,2'-Methylene-bis [3, 4, 6-trichloro ${{\beta}-(c-methyl-p-nitroanilino)$ propionoxy} benzene]; m.p. $163-164^{\circ}C,\;C_{33}H_{26}O_8N_4Cl_6$-were synthesized by Mannich reaction from 2,2'-Methylene-bis (3, 4, 6-trichloroacetoxy benzene) and their antimicrobial activities against the microorganisms Staphylococcus aureus, Escherichia coli, Bacillus subtilis Natto, Brevibacterium ammoniagenes, Candida tropicalis, Rhodotorula glutinis, Pseudomonas ovalis, Aspergillus candidus Link, Aspergillus awamori Nakazawa. Aspergillus niger var. Tieghem, Aspergillus usami Sakakuchi, Penicillium notatum-were tested. 2,2'-methylene-bis [3, 4, 6-trichloro ${{\beta}-(o-nitroanilino)$ propionoxy} benzene] showed a strong antimicrobial activity against Bacilus subtilis Natto and Brevibacterium ammoniagenes.

• Journal of environmental and Sanitary engineering
• /
• v.11 no.2
• /
• pp.33-41
• /
• 1996

This study was performed to examine the factors influencing on the degradation of TCE, Benzene and 2,4 DCP in aqueous solution using ultrasonic irradiation. The TCE,Benzene and 2,4 DCP, which are hazard compounds causing environmental pollution, were not decomposable pollutants by convientional treatment. The results shows that the generation of H$_{2}$O$_{2}$, H$^{+}$ and OH$^{-}$ radical was formed by the oxidation and reduction reaction of ultrasound, and then theses decomposed the refractory pollutants of TCE, Benzene & 2,4 DCP in aqueous solution. we conformed that the ultrasonic irradiation was excellent in removal efficiency of the refractory pollutants any other than Advanced Oxidation Processes(AOP), utilized the treatment of organic compounds in the industrial wastewater. Consequently, these results suggest that ultrasonic irradiation may be extremely useful for the treatment of wastewaters contaminated organic pollutants, which is difficult to treat economically by conventional process.

• Journal of Korean Society for Atmospheric Environment
• /
• v.18 no.E1
• /
• pp.13-20
• /
• 2002

The electrical and chemical properties of the dielectric barrier discharge (DBD) process for the benzene removal were investigated. The benzene removal was initiated with the applied voltage higher than the discharge onset value. The removal efficiency over 95 % was obtained at approximately 1.6 kJ lite $r^{r-1}$ of the electrical energy density. The increase of the inlet concentration decreased the removal efficiency. However, the benzene decomposition rate increased with the inlet concentration . While the increase of the gas retention time enhanced the removal efficiency, the decomposition rate decreased. Identification of the optimum condition between the decomposition rate and the removal efficiency is required for field applications of the DBD process.s.

• Environmental Engineering Research
• /
• v.13 no.1
• /
• pp.14-18
• /
• 2008

Photocatalytic oxidations of benzene gas using the closed system (batch reactor) were induced to determine its by-products and investigate the effect of humidity and oxygen concentration on their generation. The study was able to identify 11 gaseous by-products: 2-methylpropene, acetaldehyde, acetone, pentane, methylcyclobutane, methylcyclopentane, cyclohexane, 2,3-dimethylbutane, 2-methylpentane, 3-methylpentane, and hexane. All the by-products were saturated hydrocarbons, which are less toxic than benzene and were probably formed through hydrogenation reaction on the photocatalytic surface. The photocatalytic oxidation of benzene under higher humidity produced less by-products. However, the amount of acetone released increased with higher humidity and oxygen concentration.

• Journal of environmental and Sanitary engineering
• /
• v.16 no.3
• /
• pp.72-79
• /
• 2001

The selective catalytic oxidation of toxic aromatic solvents (benzene, toluene, ethylbenzene, and styrene) and their mixtures were studied on a $Pt/{\;}{\gamma}-Al_2O_3$ catalyst at temperature ranging from $160~350^{\circ}C$. The deep conversion of aromatic solvents was increased as the inlet concentration was decreased and the reaction temperature was increased. The reactivity increases in order benzene > toluene > ethylbenzene > styrene. In mixture, remarkable effects on reaction rate and selectivity have been evidence ; the strongest inhibition effect is shown by styrene and increase in a reverse order with respect to that of reactivity. The inhibition effect was increased in order styrene > ethylbenzene > toluzene > benzene. This trend is due to the competition adsorption between the two or three reactants on the oxidized catalyst. Also, the deep conversion change of benzene was a small in tertiary mixtures(including of benzene and styrene) comparing with conversion characteristics of binary mixture with styrene. This result was due to small concentration of styrene. which had very strong inhibition effect.

• 한국생물공학회:학술대회논문집
• /
• 2000.11a
• /
• pp.179-182
• /
• 2000

Toluene-degrading bacterium, Microbacterium esteraromaticum CS3-1 was isolated from the biofilter for the removal of BTEX. Microbacterium esteraromaticum CS3-1 was shown to utilize toluene as a primary carbon and energy source. Effect of mixed BTEX gases on toluene degradation rate by M. esteraromaticum CS3-1 was investigated in this study. Toluene degradation rate was 2.26(only toluene), 2.06(toluene+benzene), 2.57(toluene+ethylbenzene), and 4.74(toluene+xylene) mmole $toluene\;{\cdot}\;g-DCW^{-1}\;{\cdot}\;h^{-1}$. Toluene degradation rate was 2.26(only toluene), 1.23(toluene+benzene+ethylbenzene), 1.52 (toluene+ethylbenzene+xylene), and 1.76(toluene+benzene+ethylbenzene+xylene) mmole $toluene\;{\cdot}\;g-DCW^{-1}\;{\cdot}\;h^{-1}$. The presence of BTEX compounds over three mixtures had a negative effect on toluene degradation rate. Toluene degradation rates were enhanced by the presence of ethylbenzene or xylene, whereas the presence of benzene had a negative effect on toluene degradation rate in comparison with toluene degradation rate when only toluene is existent.

• 한국생물공학회:학술대회논문집
• /
• 2000.11a
• /
• pp.163-166
• /
• 2000

Hydrogen sulfide, ammonia and benzene which are generated from natural leather industry were simultaneously removed using biofilter including benzene degrading microbial consortia and sulfur oxidizer Thiobacillus sp.IW. The removal efficiency of benzene was maintained 90% in average for single and mixed gas treatment and that of ammonia was 99%, whereas at of hydrogen sulfide was relatively lower 85%.

• Journal of the Korean Chemical Society
• /
• v.22 no.4
• /
• pp.254-258
• /
• 1978

A simple and sensitive method of determining trace amounts of benzene hexachloride (BHC) in air has been investigated. The sample is passed through the n-hexane solution and the absorbance of it was measured at 245nm spectrophotometrically and the concentration of benzene hexachloride was calculated using a working curve obtained from the vaporized standard benzene hexachloride passed into n-hexane.

• Journal of the Korean Chemical Society
• /
• v.41 no.2
• /
• pp.82-87
• /
• 1997

The 1,4-bis(alkyldichlorosilyl)benzene was synthesized to be a precursor of the bis(silacyclopentadienyl) aromatic system. The cyclization reaction of the precursor with 1,4-dilithio-1,2,3,4-tetraphenyl-1,3-butadiene produced the 1,4-bis(1'-alkyl-2',3',4',5'-tetraphenyl-1'-silacyclopentadienyl)benzene as the ligand of organotransition metal compound and the precursor of the stable silacyclopentadienyl anion.

• Bulletin of the Korean Chemical Society
• /
• v.18 no.3
• /
• pp.328-333
• /
• 1997

Dicyanovinyl-containing bis-hydroxy monomers, p-bis[1-(4-hydroxypiperidinyl)]-2,2-dicyanovinyl]benzene (2), p-bis[1-[1-(2-hydroxyethyl)piperazinyl]-2,2-dicyanovinyl]benzene (3), p-bis[1-(4-hydroxyphenylamino)-2,2-dicyanovinyl]benzene (4) and p-bis[1-[N-methyl-(N-hydroxyethyl)amino]]-2,2-dicyanovinyl]benzene (5) were prepared from p-bis(1-chloro-2,2-dicyanovinyl)benzene (1) and the corresponding amino alcohol. The poly(enaminonitriles-ester)s with a variety of chemical structures in the main chain were prepared from them. The chemical structure of polymers was confirmed through the syntheses of their corresponding model compounds. The polymers are easily soluble in polar aprotic solvents such as DMF, DMSO and NMP. Brittle and hard films can be cast from DMF solutions of polymers. Most polymers showed a large exotherm in DSC analyses and undergo a curing reaction around 350 ℃ to form insoluble materials. The polymers consisting of rigid aromatic moieties show 80-88% residual weight at 500 ℃ under nitrogen.