• Title/Summary/Keyword: p-xylene

Search Result 322, Processing Time 0.023 seconds

Evaluation of softening ability of Xylene & Endosolv-R on three different epoxy resin based sealers within 1 to 2 minutes - an in vitro study

  • Shenoi, Pratima Ramakrishna;Badole, Gautam Pyarelal;Khode, Rajiv Tarachand
    • Restorative Dentistry and Endodontics
    • /
    • v.39 no.1
    • /
    • pp.17-23
    • /
    • 2014
  • Objectives: This study evaluated the efficacy of Endosolv-R and Xylene in softening epoxy resin based sealer after 1 to 2 min exposure. Materials and Methods: Sixty Teflon molds ($6mm{\times}1.5mm$ in inner diameter and depth) were equally divided into 3 groups of 20 each. AH 26 (Dentsply/De Trey), AH Plus (Dentsply/De Trey), Adseal (Meta-Biomed) were manipulated and placed in the molds allotted to each group and allowed to set at $37^{\circ}C$ in 100% humidity for 2 wk. Each group was further divided into 2 subgroups according to the solvents used, i.e. Xylene (Lobachemie) and Endosolv-R (Septodont). Specimens in each subgroup were exposed to respective solvents for 1 and 2 min and the corresponding Vicker's microhardness (HV) was assessed. Data was analysed by Mauchly's test and two-way analysis of variance (ANOVA) with repeated measures, and one-way ANOVA. Results: Initial hardness was significantly different among the three sealers with AH Plus having the greatest and Adseal having the least. After 2 min, Xylene softened AH Plus and Adseal sealer to 11% and 25% of their initial microhardness, respectively (p < 0.001), whereas AH 26 was least affected, maintaining 89.4% of its initial microhardness. After 2 min, Endosolv-R softened AH 26, AH Plus and Adseal to 12.7, 5.6 and 8.1% of their initial microhardness, respectively (p < 0.001). Conclusions: Endosolv-R was a significantly more effective short term softener for all the tested sealers after 2 min whereas Xylene was an effective short term softener against AH plus and Adseal but less effective against AH 26.

Studies on Atomic Absorption Spectrophotometric Analysis of Hexavalent Chromium in Waste Water by Solvent Extraction (용매 추출법에 의한 폐수중 6가크롬의 원자흡수 분광분석에 관한 연구)

  • Eung-Pyo Kim;Young-Sang Kim
    • Journal of the Korean Chemical Society
    • /
    • v.30 no.5
    • /
    • pp.423-432
    • /
    • 1986
  • Atomic absorption spectrophotometric (AAS) determination of hexavalent chromium [Cr(VI)] in a waste water was studied. Cr(VI) was extracted with p-xylene from the wastewater, in the way of ion pair formation with anion exchanger aliquat-336(tri-caprylmethyl ammonium chloride). 100ml waste water, after organic materials were extracted out with toluene, was acidified with conc. HCl adjusting the medium to pH 0.5 and 20ml of p-xylene containing 0.01M aliguat-336 was used to extract Cr(VI) from the acidified solution. The absorbance of chromium was measured with air-acetylene flame at 357.9nm. Standard addition method was used in the determining concentration of Cr(VI) extracted. No interference has been found in the extraction of Cr(VI) by the Al(III), Fe(III) and Cr(III) ion presented. However, Fe(II) decreased the absorbance of Cr(VI), due to the fact Fe(II) reduces Cr(VI) to Cr(III). The contained organic material was removed prior to extracting process, since it may reduced the absorbance of Cr(VI). The recovery of added Cr(VI) was over 96%, which seems to be promising and the relative standard deviation was 3.95%

  • PDF

Temporal and Spatial Distribution of VOCs in Seawater of Kwangyang Bay (광양만 해수의 휘발성 유기화합물에 대한 시.공간적 분포)

  • 주현수;이우범;박종천
    • Korean Journal of Environmental Biology
    • /
    • v.17 no.4
    • /
    • pp.513-519
    • /
    • 1999
  • Volatile organic compounds (VOCs) were analyzed on the seawater from 17 stations in Kwangyang Bay throughtout the year. We could not detect 10 VOCs; methylene chloride, tetrachloromethane, 1, 1, 1-trichloroethane, trichloroethane, 1, 1, 1, 2-tetrachloroethane, trichloroethylene, bromoethane, dibromoethane, bromobenzene, 1-ethyl-3-methylbenzene. The other VOCs-chloroform, 1, 2-dichloroethane, ethylbenzene, benzene, toluene, m, p-xylene, methylethylketone, styrene, hexane-were detected with a little variance according to the sampling stations and the sampling seasons. The concentrations of chloroform (0.6 ~ 49.9 $\mu$g/1) and toluene (0.42 ~ 48.3 $\mu$g/1) were high and they were detected more frequently than the other detected VOCs. We also tried to seek the correlation between the physicochemical environmental factors and VOCs. Only toluene had the high correlation coefficient with the water temperature (r = -0.524) and with the pH (r = 0.319). Correlation between VOCs themselves showed some interesting results. The benzene had high correlation coefficient (r = 0.549 ~ 0.662) with three VOCs such as toluene, m, p-xylene, ethylbenzene. From these results it is suggested that VOCs might be discharged simultaneously in Kwangyang Bay.

  • PDF

Characteristics of Source and Concentration of VOCs in Daegu (대구지역 대기 중 VOCs 농도 및 발생원 특성)

  • Gu Min-Jung;Choi Sung-Woo
    • Journal of Environmental Science International
    • /
    • v.14 no.6
    • /
    • pp.543-553
    • /
    • 2005
  • In recent days, photochemical smog due to the rapid industry development and vehicle increasement has become a critical pollutant in the metropolitan area and the number of ozone alarm signal has increased every year. This research was performed to evaluate VOCs emission source characteristics and concentration of VOCs in Daegu. The site average concentration was observed in the following order: industrial area > commercial area > residential area. Most of the VOCs species except toluene showed variations with higher concentration during nighttime, and lower concentration during the daytime. The major VOCs of stationary emission source were BTEX(benzene, toluene, ethylbenzene. xylene) and methylene chloride, trichloroethene and styrene. Also, those of automobile exhaust were toluene and benzene. Also, the major VOCs concentration emited by the vehicle fuel was observed in the following order: gasoline > light oil > liquefied petroleum gas (L.P.G). Correlation coefficients values were estimated between major VOCs such as toluene, ethylbenzene, m,p-xylene, o-xylene. Results showed that correlation coefficient values were significant magnitude above 0.76. Also, there showed highly significant correlations among ethyl benzene, m,p-xylene, and o-xylene concentration(Pearson correlation coefficients, r=0.868-0.982). Calculated correlation coefficients among commercial area,industrial area and residential area were 0.934-0.981, they showed high correlation. There showed highly correlation between stationary emission source and industrial area, compared with commercial area and residential area. Also, calculated correlation coefficients among commercial area, industrial area, residential area and automobile exhaust were 0.732, 0.725, 0.777, respectively.

Comparative Measurements and Characteristics of Cu Diffusion into Low-Dielectric Constant para-xylene based Plasma Polymer Thin Films

  • Kim, K.J.;Kim, K.S.;Jang, Y.C.;Lee, N.-E.;Choi, J.;Jung, D.
    • Journal of the Korean institute of surface engineering
    • /
    • v.34 no.5
    • /
    • pp.475-480
    • /
    • 2001
  • Diffusion of Cu into the low-k para-xylene based plasma polymer (pXPP) thin films deposited by plasma-enhanced chemical vapor deposition using the para-xylene precursor was comparatively measured using various methods. Cu layer was deposited on the surfaces of pXPPs treated by $N_2$ plasma generated in a magnetically enhanced inductively coupled plasma reactor. Diffusion characteristics of Cu into pXPPs were measured using Rutherford backscattering spectroscopy (RBS), secondary ion mass spectroscopy (SIMS), cross-sectional transmission electron microscopy (XTEM), and current-voltage (I-V) measurements for the vacuum-annealed Cu/pXPPs for 1 hour at $450^{\circ}C$ and were compared. The results showed a correlation between the I-V measurement and SIMS data are correlated and have a sensitivity enough to evaluate the dielectric properties but the RBS or XTEM measurements are not sufficient to conclude the electrical properties of low-k dielectrics with Cu in the film bulk. The additional results indicate that the pXPP layers are quite resistant to Cu diffusion at the annealing temperature of $450^{\circ}C$ compared to the other previously reported organic low-k materials.

  • PDF

Continuous Measurements of Aromatic VOCs in a Mid-eastern Region of Seoul during Winter 2002/2003 (방향족 휘발성 유기화합물의 겨울철 연속 관측 연구)

  • 최여진;오상인;김기현
    • Journal of Korean Society for Atmospheric Environment
    • /
    • v.19 no.5
    • /
    • pp.491-502
    • /
    • 2003
  • In the present work, the distribution characteristics of ambient volatile organic compounds (VOCs) were investigated at high temporal resolution from a monitoring station located in a mid-eastern area of Seoul. A total number of 587 samples were collected during December 2002 to January 2003. The measurements of VOC were conducted by a combination of on-line air sampling and thermal desorption unit (TDU) coupled with capillary GC/FID analysis. A total of five aromatic compounds (BTEX: benzene, toluene, ethylbenzene, m, p-xylene, and o-xylene) were measured routinely at hourly intervals during the whole study period. The mean concentrations of BTEX measured in our study period were found in the order: toluene (8.99 $\pm$5.38 ppb) > benzene (0.92$\pm$0.52 ppb) > m, p-xylene (0.51$\pm$0.34 ppb) > 0- xylene (0.48$\pm$0.35 ppb) > ethyl benzene (0.43$\pm$ 0.32 ppb). The BTEX concentrations were generally higher during the daytime than the nighttime, exhibiting certain patterns on a weekly basis. Results of our analysis indicate that the unusually high concentrations of toluene, while showing good correlations with other VOCs, can be a good indicator of air pollution in the study area.

Blocking of Zeolite Pore by Loading Ni-Pt Nanoparticles for Maximization of Isomerization Selectivity

  • Bhavani, A. Geetha;Reddy, N. Subba
    • Korean Chemical Engineering Research
    • /
    • v.58 no.4
    • /
    • pp.658-664
    • /
    • 2020
  • Zeolite HY is wet impregnated with Ni (0.1, 0.3, 0.4, 0.5 wt%), Pt (0.1 wt%) and reduced in presence of hydrogen to form nanosized particles of Ni and Pt. All the catalysts were characterized by XRD, TEM, ESCA, NH3-TPD, Pyridine adsorbed FT-IR and BET. Characterization results confirm that the Ni and Pt fractions effectively rehabilitated the physio-chemical properties of the zeolite HY catalysts. Further, all the reduced catalyst were screened with hydroisomerization of m-xylene at LHSV = 2.0 h-1 in the temperature range 250-400 ℃ in steps of 50 ℃ in hydrogen atmosphere (20 ml/g). The addition of Ni to Pt catalyst increases hydroisomerization conversion, as well as maximizes p-xylene selectivity by restricting the pore size. The increasing trend in activity continues up to 0.3 wt% of Ni and 0.1 wt% Pt addition over zeolite HY. The increasing addition of Ni increases the total number of active metallic sites to exposed, which increases the metallic sites/acid sites ratio towards the optimum value for these reactions by better balance of synergic effect for stable activity. The rate of deactivation is pronounced on monometallic catalysts. The results confirm the threshold Ni addition is highly suitable for hydroisomerization reaction for product selectivity over Ni-Pt bimetallic/support catalysts.

Analysis and estimation of the BTEX using Canister­GC/MS in Seongseo Industrial Complex (Canister와 GC/MS를 이용한 대구성서산업단지의 BTEX의 분석 및 평가)

  • Kim Tae-Sub;Choi Sung-Woo
    • Journal of Environmental Science International
    • /
    • v.14 no.3
    • /
    • pp.351-358
    • /
    • 2005
  • The research in this paper was carried out to examine the BTEX(Benzene, Toluene, Ethylbenzene, Xylene) concentrations in Seongseo Industrial Complex. These compounds are the major constituents, more than $60\%$ in composition of total VOCs, mainly charging in ambient air. BTEX samples were collected from the 38 sites, 10 for the source points and 18 for the boundary sites, and were analyzed by canister-GC/MS. The mean concentrations of BTEX were 33 ppbv for benzene, 214 ppbv for toluene, 89 ppbv for ethyl benzene, 77 ppbv for xylene. Among the BTEX, toluene had the highest concentration in the source points and boundary sites. In the source points, BTEX concentration of incineration facility for hazardous wastewater appeared highly in the range of 220­350 ppbv. BTEX concentrations in source boundary sites appeared in the order of toluene>ethylbenzene>xylene>benzene. As a result of the correlation analysis, the concentration of the source points was related to those of the boundary sites. Correlation of ethylbenzene and xylene was presented to 0.7991(P<0.0 1),\;0.6329(P<0.05) as the correlation coefficient, respectively.

Studies of Ambient BTEX Distribution Characteristics in the Nan-Ji-Do Landfill Site in Seoul (난지도를 중심으로 한 대기 중 BTEX 성분의 농도분포 특성에 대한 연구)

  • 김기현;김민영;오상인;윤중섭;이강웅
    • Journal of Korean Society for Atmospheric Environment
    • /
    • v.17 no.6
    • /
    • pp.463-474
    • /
    • 2001
  • In this study, the concentrations of major anthropogenic volatile organic compounds(VOCs) which include benzene, toluene, m, p-xylene, o-xylene, and ethylbenzene were measured at the Nan-ji-do landfill site during the spring and fall season of 2000. the temporal distribution characteristics of these VOCs were investigated over varying time scale. According to our study, the mean concentration of those species were computed to be 1.65$\pm$2.68(benzene), 9.62$\pm$9.32(toluene), 1.84$\pm$2.90(m, p-xylene), 0.83$\pm$1.43(o-xylene), and 1.17$\pm$1.21 ppb(ethylbenzene). The VOCs levels in the study area are not distinctively higher than the level typically found in urban area that can be subject to the influence of various anthropogenic source processes. Inspection of their temporal trends exhibited various patterns for the diurnal(and seasonal) cycle. Although each species showed distinctive patterns in temporal distribution trends, we were able to find the strong correlations among most concurrently measured VOCs except for benzene.

  • PDF