• Journal of the Korean Chemical Society
• /
• v.25 no.2
• /
• pp.75-84
• /
• 1981

Ultraviolet spectrophotometric investigations have been carried out on the systems of mesitylene with iodine, bromine, iodine monochloride and iodine monobromide in carbon tetrachloride. The results reveal the formation of the charge transfer complexes of the type, $C_6H_3(CH_3)_3{\cdot}X_2$ or $C_6H_3(CH_3)_3{\cdot}IX$ (X denotes halogen atoms). The equilibrium constants were obtained in consideration of that absorption maxima due to the formation of the charge transfer complexes shift to blue with the increasing temperatures. Thermodynamic parameters, ${\Delta}H$, ${\Delta}G$ and ${\Delta}S$ for the formation of the charge transfer complexes were calculated from these values. These results indicate that the relative stabilities of the mesitylene complexes at each temperature decrease in the order, ICl > IBr > $I_2$ > $Br_2$. This order may be a measure of their relative acidities toward mesitylene, which is explaned in terms of the relative polarizabilities of halogen molecules and the relative electronegativities of halogen atoms. These results combined with previous study of this series indicated that the relative stabilities of the polymethylbenzene complexes with iodine increase in the order Benzene < Toluene < Xylene < Mesitylene Thus, analysis of these findings is discussed.

• Journal of the Korean Chemical Society
• /
• v.11 no.3
• /
• pp.89-93
• /
• 1967

The interactions of fluorobenzene with iodine monochloride, iodine monobromide, bromine and chlorine in carbon tetrachloride solution have been examined through ultraviolet spectrophotometric measurements. The results indicate the formation of one to one molecular complexes, $C_6H_5F{\cdot}ICl$, $C_6H_5F{\cdot}IBr$, $C_6H_5F{\cdot}Br_2$, and $C_6H_5F{\cdot}Cl_2$ in solution. The equilibrium constants obtained at room temperature for the formation of these four complexes are 0.161, 0.072, 0.045 and 0.035 l $mole^{-1}$, respectively. Comparison of these results with those reported in the literature on other complexes of similar type reveals that the relative stabilities of these complexes decrease in the following orders: ICl>IBr>$I_2$>$Br_2$>$Cl_2$ $C_6H_6$>$C_6H_5Br$>$C_6H_5Cl$>$C_6H_5F$

• Journal of the Korean Chemical Society
• /
• v.11 no.3
• /
• pp.94-99
• /
• 1967

The interactions of iodobenzene with iodine, iodine monobromide, iodine monochloride and chlorine in carbon tetrachloride solution have been investigated by means of ultraviolet spectrophotometric measurements. The results reveal the formation of one to one molecular complexes, $C_6H_5I{\cdot}I_2$, $C_6H_5I{\cdot}IBr$, $C_6H_5I{\cdot}ICl$, and $C_6H_5I{\cdot}Cl_2$, in solution. The equilibrium constants obtained at room temperature (about $21^{\circ}C$) for the formation of these four complexes are 0.23, 0.73, 1.2 and 0.070 l $mole^{-1}$, respectively. Comparison of these results with those reported in the literature on other complexes of similar type indicates that the relative stabilities of these complexes decrease in the following orders: ICl>IBr>$I_2$>$Br_2$>$Cl_2$ $C_6H_5I$>$C_6H_6$>$C_6H_5Br$>$C_6H_5Cl$>$C_6H_5F$.

• KSBB Journal
• /
• v.16 no.3
• /
• pp.281-285
• /
• 2001

Biofiltration of volatile organic compounds (VOCs) was performed for 80 days in a biofilter packed with peat. The empty bed residence time was 3.2 min. for a gas mixture of isoprene, dimethyl sulfide, chloroform. benzene, trichlorethylene, toluene, m0xylene, o-xylene and styrene. After 34 days of acclimatization the removal efficiency for a 83 g/㎥ gas input was 93% at $25^{circ}C$ and 73% at $45^{circ}C$, respectively. The maximum cell density at $25^{circ}C$ was 1.12$\times$10(sup)8 cells/g. Removal efficiencies of m-xylene and toluene (91%) were better than that of benzene (86%). The first quarter of the packed column removed 60% of the incoming VOCs.

• Journal of the Korean Chemical Society
• /
• v.25 no.1
• /
• pp.1-6
• /
• 1981

Ultraviolet spectrophotometric investigations were carried out on the systems of o-, m-and p-xylene with iodine in carbon tetrachloride. The results reveal the formation of one to one molecular complexes of the type, $C_6H_4(CH_3)_2{\cdot}I_2. $The equilibrium constants of complexes were obtained in consideration of that absorption maxima has the blue shift with the increasing temperatures according to the formation of the charge transfer complexes. The thermodynamic parameters, $ {\Delta}$H, $ {\Delta}$G and $ {\Delta}$S for the formation of the charge transfer complexes were calculated from these values. These results combined with previous study of this series indicated that the relative stabilities of the polymethylbenzene complexes with iodine increase in the order, Benzene < Toluene < o-Xylene < p-Xylene These results are supposed to be the influence resulted from increase of electron density by the positive inductive effect and the steric hindrance effect.

• Journal of the Korean Chemical Society
• /
• v.29 no.6
• /
• pp.575-581
• /
• 1985

Ultraviolet spectrophotometric investigations have been carried out on the systems of benzene, naphthalene and phenanthrene with iodine in carbon tetrachloride. The results reveal the formation of the one to one molecular complexes. The equilibrium constants were obtained in consideration of that absorption maxima due to the formation of the charge transfer complexes shift to blue with increasing temperature. Thermodynamic parameters for the formation of the charge transfer complexes were calculated from these values. These results indicate that the stabilities of the complexes formed between polynuclear aromatics and iodine increase with the number of aromatic rings. This may be a measure of the relative basicities of polynuclear aromatics toward iodine, which is explained in terms of the resonance of the interaction between aromatics and iodine. The results in this study were, additionally, compared with those of the polymethylbenzene series to be discussed the reason for them.

• Journal of the Korean Chemical Society
• /
• v.19 no.5
• /
• pp.343-350
• /
• 1975

About 20${\sim}$100${\mu}g$ iridium have been extracted quantitatively as stannous-chloro Complex from aqueous solution by Alamine-336, a high molecular weight tertiary amine, dissolved in benzene. The extractability was confirmed by radioactive tracer of iridium-192. The spectrophotometric measurements of the extracted species at 322.5 nm indicate the feasibility of this method to be used as an analytical procedure for the determination of micro amount of iridium. An anion model of stannous-chloro complex of iridium has been postulated to account for the extraction mechanism.

• Proceedings of the Korean Society of Dyers and Finishers Conference
• /
• 2012.03a
• /
• pp.52-52
• /
• 2012

Poly(phenylene sulfide)(PPS)는 내열성 및 내화학성이 뛰어난 고분자 소재로, 대표적인 엔지니어링 플라스틱 중 하나이다. PPS는 벤젠 링에 황원자가 파라 치환 형태로 교대로 존재하는 결정성 고분자이며, 다른 대부분의 고성능 섬유고분자가 용융되지 않는 것과는 달리 용융되는 열가소성 소재이다. PPS는 높은 내약품성과 열에 대한 장기적인 안정성을 나타내고, 방염제 첨가 없이도 방염화가 가능하며, 전기 절연성이 뛰어나고, 형태안정성도 우수하다. 또한 $200^{\circ}C$ 이하에서는 어떤 용매에도 용해되지 않으며, $200^{\circ}C$ 이상에서도 몇 가지 방향족 화합물에만 제한된 범위 내에서 용해되는 우수한 내약품성을 나타낸다. PPS의 내열성을 더욱 우수하게 하기 위해 고분자 사슬을 가교할 수 있다. 가교에는 열처리 또는 감마선, 전자선, 자외선 조사를 이용할 수 있는데 열에 의한 가교는 균일한 열전달과 고온이 필요하며 감마선 및 전자선 조사는 설비의 고비용과 방사선 노출 위험으로 인해 비친환경적이다. 반면에 자외선 조사법은 다루기 쉽고 비용이 적게 들고 친환경적인 장점을 가진다. 본 연구에서는 PPS film의 열안정성을 향상시키기 위해 자외선 조사를 이용하여 PPS film의 광가교를 수행하였다.

• Journal of the Korean Chemical Society
• /
• v.9 no.4
• /
• pp.215-221
• /
• 1965

The significant liquid structure theory is extended to binary mixture, benzene-ethylenechloride system. The partition function, applicable throughout the temperature range in which Raoult's law is satisfied is derived. The thermodynamic quantities such as total and partial pressures, molar volumes and mixing entropies are calculated from the partition function at the temperatures $293.15^{\circ},\;323.14^{\circ}\;and\;357.15^{\circ}K.$ The theoretical values, thus calculated, are found to agree with the experimental data in the literatures.

• Clean Technology
• /
• v.19 no.4
• /
• pp.416-422
• /
• 2013

In environmental friendly aspects, the synthesis of glycerol carbonate from glycerol using carbon monoxide and oxygen gases which were produced in petrochemical plants was studied. The oxidative carbonylation of glycerol under batch reaction system was performed on parameter conditions such as effect of various metals (Cu, Pd, Fe, Sn, Zn, Cr), oxidizing agents, mole ratio of carbon monoxide to oxygen, catalyst amount, solvent types, reaction temperature and time and dehydrating agents. In particular copper chloride catalysts showed the excellent activities, and the glycerol carbonate yields over CuCl and $CuCl_2$ catalysts were the maximum of 44% and 64%, respectively at the following reaction conditions: solvent as nitrobenzene, mole ratio of 1:3:0.15 (glycerol:carbon monoxide:catalyst), mole ratio of 2:1 (carbon monoxide:oxygen), the total pressure of 30 bar at 413 K for 4 hr. It was found that reactivity were significantly different depending on the oxidation number of Cu catalysts, and oxygen plays an important role as oxidizing agents in producing H2O during oxidation reaction after carbonylation of glycerol.