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Journal articles on the topic 'Chlorinated hydrocarbon'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Huang, Li Kun, and Guang Zhi Wang. "Study on Species and Distribution of Volatile Organic Compounds in WWTP." Advanced Materials Research 864-867 (December 2013): 2035–38. http://dx.doi.org/10.4028/www.scientific.net/amr.864-867.2035.

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This study carried on a qualitative analysis on emission and distribution of VOCs and quantitative analysis on BTEX and chlorinated hydrocarbon emitted from a municipal wastewater treatment plant (WWTP). At the same time, the variations of BETX and chlorinated hydrocarbon in three-phases in the biological treatment process in lab-scale were investigated. Results revealed that the low molecular weight hydrocarbon, BTEX (benzene, toluene, xylene) and chlorinated hydrocarbons (chloroform, carbon tetrachloride, chlorylene, tetrachloroethylene) were the main components of VOCs. Primary clarifier volatilized thirty-three species of VOCs, which was most in the WWTP. The remaining organic compounds in this unit belonged to refractory organics that was hardly decomposed by microbe. The more complex aromatic compounds in VOCs were detected.

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2

MURAKAMI, Takehiko. "Chlorinated hydrocarbon solvent." Journal of the Japan Society for Precision Engineering 54, no. 10 (1988): 1862–66. http://dx.doi.org/10.2493/jjspe.54.1862.

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3

ARMSTRONG, S., and L. GREEN. "Chlorinated hydrocarbon solvents." Clinics in Occupational and Environmental Medicine 4, no. 3 (August 2004): 481–96. http://dx.doi.org/10.1016/j.coem.2004.03.005.

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4

Sallmén, Markku, Sanni Uuksulainen, Christer Hublin, Aki Koskinen, and Markku Sainio. "O2D.5 Risk of parkinson disease in solvent exposed workers in finland." Occupational and Environmental Medicine 76, Suppl 1 (April 2019): A19.2—A19. http://dx.doi.org/10.1136/oem-2019-epi.51.

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Epidemiologic studies indicate that occupational exposure to solvents may increase risk of Parkinson disease (PD).We constructed a population-based case-control study of incident PD using a register of Reimbursement of medicine costs of the Social Insurance Institution of Finland, along with the Population Information System, including census records for all Finnish residents. PD cases were diagnosed between 1995–2014. Controls were randomly selected from the population while matching on diagnosis year, birth year (1930–1950), and sex. A total of 11,757 PD cases and 23 236 controls had data from the occupational census in 1990, ensuring ≥4 years exposure lagging and 21 years of occupational history data (5 censuses from 1970–1990). We used the Finnish Job Exposure Matrix to assess cumulative exposure (CE) to four groups of solvents (aliphatic/alicyclic hydrocarbon, aromatic hydrocarbon, chlorinated hydrocarbon, other). We estimated PD-solvent odds ratios (ORs) and 95% confidence intervals (CIs) using unconditional logistic regression, while adjusting for age, sex, socioeconomic status and smoking (a_OR), or additionally for CE to chromium and one of the other solvent groups (ab_OR).In total, 3758 cases (30.4%) and 7445 controls (32.0%) were potentially exposed to solvents (a_OR 0.99; CI: 0.94–1.05). Exposure to chlorinated hydrocarbons was associated with PD (a_OR 1.20; CI: 1.05–1.36; ab_OR 1.21 CI: 1.04–1.40) at the highest CE group (20–145 ppm-years, n=409 cases and 728 controls) but not at lower CE levels. Overall, CE to chlorinated hydrocarbons (n=1840 cases and 3693 controls) was associated with increased risk of PD (p-for-trend=0.01). There was no evidence of a positive association for any of the other solvent groups.We observed a positive association between occupational exposure to chlorinated hydrocarbons and risk of PD. This was especially true for greatest duration and/or level of exposure.

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5

Ohura, Takeshi, Maki Morita, Masakazu Makino, Takashi Amagai, and Kayoko Shimoi. "Aryl Hydrocarbon Receptor-Mediated Effects of Chlorinated Polycyclic Aromatic Hydrocarbons." Chemical Research in Toxicology 20, no. 9 (September 2007): 1237–41. http://dx.doi.org/10.1021/tx700148b.

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6

Li, Hui, Zhantao Han, Yong Qian, Xiangke Kong, and Ping Wang. "In Situ Persulfate Oxidation of 1,2,3-Trichloropropane in Groundwater of North China Plain." International Journal of Environmental Research and Public Health 16, no. 15 (August 1, 2019): 2752. http://dx.doi.org/10.3390/ijerph16152752.

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In situ injection of Fe(II)-activated persulfate was carried out to oxidize chlorinated hydrocarbons and benzene, toluene, ethylbenzene, and xylene (BTEX) in groundwater in a contaminated site in North China Plain. To confirm the degradation of contaminants, an oxidant mixture of persulfate, ferrous sulfate, and citric acid was mixed with the main contaminants including 1,2,3-trichloropropane (TCP) and benzene before field demonstration. Then the mixed oxidant solution of 6 m3 was injected into an aquifer with two different depths of 8 and 15 m to oxidize a high concentration of TCP, other kinds of chlorinated hydrocarbons, and BTEX. In laboratory tests, the removal efficiency of TCP reached 61.4% in 24 h without other contaminants but the removal rate was decreased by the presence of benzene. Organic matter also reduced the TCP degradation rate and the removal efficiency was only 8.3% in 24 h. In the field test, as the solution was injected, the oxidation reaction occurred immediately, accompanied by a sharp increase of oxidation–reduction potential (ORP) and a decrease in pH. Though the concentration of pollutants increased due to the dissolution of non-aqueous phase liquid (NAPL) at the initial stage, BTEX could still be effectively degraded in subsequent time by persulfate in both aquifers, and their removal efficiency approached 100%. However, chlorinated hydrocarbon was relatively difficult to degrade, especially TCP, which had a relatively higher initial concentration, only had a removal efficiency of 30%–45% at different aquifers and monitoring wells. These finding are important for the development of injection technology for chlorinated hydrocarbon and BTEX contaminated site remediation.

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7

Luekittisup, Prapaporn, Visanu Tanboonchauy, Jitlada Chumee, Somrudee Predapitakkun, Rattanawan W. Kiatkomol, and Nurak Grisdanurak. "Removal of Chlorinated Chemicals in H2Feedstock Using Modified Activated Carbon." Journal of Chemistry 2015 (2015): 1–9. http://dx.doi.org/10.1155/2015/959012.

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Activated carbon (GAC) was impregnated by sodium and used as adsorbent to remove chlorinated hydrocarbon (CHC) gases contaminated in H2feedstock. The adsorption was carried out in a continuous packed-bed column under the weight hourly space velocity range of 0.8–1.0 hr−1. The adsorption capacity was evaluated via the breakthrough curves. This modified GAC potentially adsorbed HCl and VCM of 0.0681 gHCl/gadsorbentand 0.0026 gVCM/gadsorbent, respectively. It showed higher adsorption capacity than SiO2and Al2O3balls for both organic and inorganic CHCs removal. In addition, the kinetic adsorption of chlorinated hydrocarbons on modified GAC fit well with Yoon-Nelson model.

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8

Huber, L. J. "Waste Water Treatment at the WACKER CHEMIE Chemical-Petrochemical Plant, Burghausen, F.R.G." Water Science and Technology 20, no. 10 (October 1, 1988): 13–19. http://dx.doi.org/10.2166/wst.1988.0119.

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Waste water treatment in larger chemical and petrochemical plants affords the application of all available technologies for pollution abatement. Elimination of conventional and priority pollutants down to low concentrations in the effluent is necessary in the F.R.G. for the protection of surface waters. Special care is directed at chlorinated hydrocarbons. The WACKER-CHEMIE plant at Burghausen which produces especially chlorinated and organic silicon compounds uses a great number of in-plant measures, pretreatment steps and finally a two-stage biological purification to attain a high effluent quality. Important in-plant measures comprise the perchlorination of all significant chloro-hydrocarbon residues and the conversion to tetrachloroethylene and the reclamation of hydrogenchloride in the production of vinylchloride. Waste waters from the manufacture of chlorinated hydrocarbons are pre-treated by steam stripping or adsorbtion to macromolecular resins. Final treatment is effected by purification in a high rate activated sludge plant followed by an aerated lagoon.

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9

Monster, Aart C. "Biological Monitoring of Chlorinated Hydrocarbon Solvents." Journal of Occupational and Environmental Medicine 28, no. 8 (August 1986): 583–88. http://dx.doi.org/10.1097/00043764-198608000-00012.

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10

SORBO, N. W., and D. P. Y. CHANG. "Observations of Chlorinated Hydrocarbon Droplet Gasification." Combustion Science and Technology 85, no. 1-6 (September 1992): 419–35. http://dx.doi.org/10.1080/00102209208947181.

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11

Acosta, Edgar, San Tran, Hirotaka Uchiyama, David A. Sabatini, and Jeffrey H. Harwell. "Formulating Chlorinated Hydrocarbon Microemulsions Using Linker Molecules." Environmental Science & Technology 36, no. 21 (November 2002): 4618–24. http://dx.doi.org/10.1021/es0158859.

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12

Baran, Jimmie R., Gary A. Pope, William H. Wade, Vinitha Weerasooriya, and Anusha Yapa. "Microemulsion Formation with Mixed Chlorinated Hydrocarbon Liquids." Journal of Colloid and Interface Science 168, no. 1 (November 1994): 67–72. http://dx.doi.org/10.1006/jcis.1994.1394.

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13

EASTWOOD, P. R., D. N. LERNER, P. K. BISHOP, and M. W. BURSTON. "Identifying Land Contaminated by Chlorinated Hydrocarbon Solvents." Water and Environment Journal 5, no. 2 (April 1991): 163–71. http://dx.doi.org/10.1111/j.1747-6593.1991.tb00603.x.

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14

Travis, Anthony S. "Detecting Chlorinated Hydrocarbon Residues: Rachel Carson’s Villains." Ambix 59, no. 2 (July 2012): 109–30. http://dx.doi.org/10.1179/174582312x13345259995967.

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15

Leo, Albert J. "Calculating the hydrophobicity of chlorinated hydrocarbon solutes." Science of The Total Environment 109-110 (December 1991): 121–30. http://dx.doi.org/10.1016/0048-9697(91)90174-d.

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16

Norstrom, Ross J., and Derek C. G. Muir. "Chlorinated hydrocarbon contaminants in arctic marine mammals." Science of The Total Environment 154, no. 2-3 (September 1994): 107–28. http://dx.doi.org/10.1016/0048-9697(94)90082-5.

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17

Boyd, T. J., M. T. Montgomery, R. H. Cuenca, and Y. Hagimoto. "Combined radiocarbon and CO2 flux measurements used to determine in situ chlorinated solvent mineralization rate." Environmental Science: Processes & Impacts 17, no. 3 (2015): 683–92. http://dx.doi.org/10.1039/c4em00514g.

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18

Rugge, C. D., and R. C. Ahlert. "Contact angle hysteresis in chlorinated hydrocarbon-water mixtures." Journal of Physical Chemistry 97, no. 34 (August 1993): 8776–79. http://dx.doi.org/10.1021/j100136a021.

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19

Kotvis, P. V., and W. T. Tysoe. "The surface chemistry of chlorinated hydrocarbon lubrication additives." Applied Surface Science 40, no. 3 (December 1989): 213–21. http://dx.doi.org/10.1016/0169-4332(89)90005-6.

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20

Richardson, Bruce J., and Gene J. Zheng. "Chlorinated hydrocarbon contaminants in Hong Kong surficial sediments." Chemosphere 39, no. 6 (September 1999): 913–23. http://dx.doi.org/10.1016/s0045-6535(99)00041-7.

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21

Kuo, Shing-Lin, and Anthony L. Hines. "Adsorption of Chlorinated Hydrocarbon Pollutants on Silica Gel." Separation Science and Technology 23, no. 4-5 (April 1988): 293–303. http://dx.doi.org/10.1080/01496398808060705.

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22

MORSE, JOHN S., and VIC A. CUNDY. "Sooting in Chlorinated Hydrocarbon Combustion—A Critical Review." Combustion Science and Technology 95, no. 1-6 (December 1993): 333–56. http://dx.doi.org/10.1080/00102209408935340.

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23

Gaggi, C., and E. Bacci. "Accumulation of chlorinated hydrocarbon vapours in pine needles." Chemosphere 14, no. 5 (January 1985): 451–56. http://dx.doi.org/10.1016/0045-6535(85)90239-5.

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24

Zuas, Oman. "WHIM-3D-QSPR APPROACH FOR PREDICTING AQUEOUS SOLUBILITY OF CHLORINATED HYDROCARBONS." Indonesian Journal of Chemistry 8, no. 1 (June 17, 2010): 65–71. http://dx.doi.org/10.22146/ijc.21650.

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The weighted holistic invariant molecular-three dimensional-quantitative structure property relationship (WHIM-3D-QSPR) approach has been applied to the study of the aqueous solubility (- log Sw) of chlorinated hydrocarbon compounds (CHC's). The obtained QSPR model is predictive and only requires four WHIM-3D descriptors in the calculation. The correlation equation of the model that is based on a training set of 50 CHC's compound has statistical parameters: standard coefficient correlation (R2) = 0.948; cross-validated correlation coefficients (Q2) = 0.935; Standard Error of Validation (SEV) = 0.35; and average absolute error (AAE) = 0.31. The application of the best model to a testing set of 50 CHC's demonstrates a reliable result with good predictability. Besides, it was possible to construct new model by applying WHIM-3D-QSPR approach without require any experimental physicochemical properties in the calculation of aqueous solubility. Keywords: WHIM-3D; QSPR; aqueous solubility; - Log Sw, chlorinated hydrocarbons, CHC's

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25

Ohura, Takeshi. "Environmental Behavior, Sources, and Effects of Chlorinated Polycyclic Aromatic Hydrocarbons." Scientific World JOURNAL 7 (2007): 372–80. http://dx.doi.org/10.1100/tsw.2007.75.

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The environmental sources and behaviors of chlorinated 2- to 5-ring polycyclic aromatic hydrocarbons (ClPAHs). ClPAHs are ubiquitous contaminants found in urban air, vehicle exhaust gas, snow, tap water, and sediments. The concentrations of ClPAHs in each of these environments are generally higher than those of dioxins but markedly lower than the concentrations of the parent compounds, PAHs. Environmental data and emission sources analysis for ClPAHs reveal that the dominant process of generation is by reaction of PAHs with chlorine in pyrosynthesis. This secondary reaction process also occurs in aquatic environments. Certain ClPAHs show greater toxicity, such as mutagenicity and aryl hydrocarbon receptor activity, than their corresponding parent PAHs. Investigation of the sources and environmental behavior of ClPAHs is of great importance in the assessment of human health risks.

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26

Schüth, Christoph, Stephan Disser, Ferdi Schüth, and Martin Reinhard. "Tailoring catalysts for hydrodechlorinating chlorinated hydrocarbon contaminants in groundwater." Applied Catalysis B: Environmental 28, no. 3-4 (December 2000): 147–52. http://dx.doi.org/10.1016/s0926-3373(00)00171-5.

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27

Senegačnik, Marjan, and Cveto Klofutar. "Self-association of cholesterol in some chlorinated hydrocarbon solvents." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 53, no. 9 (August 1997): 1495–505. http://dx.doi.org/10.1016/s1386-1425(97)00048-6.

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28

Link, R. P., W. N. Bruce, and G. C. Decker. "THE EFFECTS OF CHLORINATED HYDROCARBON INSECTICIDES ON DAIRY CATTLE." Annals of the New York Academy of Sciences 111, no. 2 (December 15, 2006): 788–92. http://dx.doi.org/10.1111/j.1749-6632.1964.tb53146.x.

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29

Dally, S., R. Garnier, and C. Bismuth. "Diagnosis of chlorinated hydrocarbon poisoning by x ray examination." Occupational and Environmental Medicine 44, no. 6 (June 1, 1987): 424–25. http://dx.doi.org/10.1136/oem.44.6.424.

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30

Frangos, Stephen A., and John M. Peters. "Chlorinated hydrocarbon solvents: Substituting our way toward human carcinogenicity." American Journal of Industrial Medicine 24, no. 4 (October 1993): 355–64. http://dx.doi.org/10.1002/ajim.4700240402.

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31

Bacci, E., and C. Gaggi. "Chlorinated hydrocarbon vapours and plant foliage: Kinetics and applications." Chemosphere 16, no. 10-12 (January 1987): 2515–22. http://dx.doi.org/10.1016/0045-6535(87)90309-2.

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32

Maguire, R. James, and Richard J. Tkacz. "Potential underestimation of chlorinated hydrocarbon concentrations in fresh water." Chemosphere 19, no. 8-9 (January 1989): 1277–87. http://dx.doi.org/10.1016/0045-6535(89)90075-1.

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33

Chihara, Kazuyuki, Caroline F. Mellot, Anthony K. Cheetham, Shani Harms, Hirotaka Mangyo, Masaki Omote, and Ryuichi Kamiyama. "Molecular simulation for adsorption of chlorinated hydrocarbon in zeolites." Korean Journal of Chemical Engineering 17, no. 6 (November 2000): 649–51. http://dx.doi.org/10.1007/bf02699112.

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34

Bylaska, Eric J. "Estimating the thermodynamics and kinetics of chlorinated hydrocarbon degradation." Theoretical Chemistry Accounts 116, no. 1-3 (December 16, 2005): 281–96. http://dx.doi.org/10.1007/s00214-005-0042-8.

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35

Staley, Laurel J., Marta K. Richards, George L. Huffman, Robert A. Olexsey, and Barry Dellinger. "Turbulent flame reactor studies of chlorinated hydrocarbon destruction efficiency." Waste Management 9, no. 2 (January 1989): 109–14. http://dx.doi.org/10.1016/0956-053x(89)90397-8.

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36

Zebarth, B. J., S. Y. Szeto, B. Hii, H. Liebscher, and G. Grove. "Groundwater Contamination by Chlorinated Hydrocarbon Impurities Present in Soil Fumigant Formulations." Water Quality Research Journal 33, no. 1 (February 1, 1998): 31–50. http://dx.doi.org/10.2166/wqrj.1998.003.

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Abstract Groundwater contamination of the Abbotsford aquifer by 1,2-dichloropropane (1,2-DCP) was reported previously. The purpose of the present study is to quantify groundwater contamination by other chlorinated hydrocarbon compounds which are present in fumigant formulations containing 1,2-DCP. Widespread contamination of 1,2,2-trichloropropane (1,2,2-TCP) was measured consistent with a non-point source. 1,2,2-TCP concentration generally decreased with depth suggesting a surface source. Localized contamination by 1,2,3-trichloro-propane, 2,3-dichloropropene and 1,3-dichloropropane was detected. Detection of these compounds was associated with higher concentrations of 1,2-DCP suggesting contamination by these compounds may have been from the same fumigant sources. The lack of a decrease in the concentration of most of these compounds over time suggests that the measured contamination will persist for some time. The results highlight the potential for persistent trace impurities in chlorinated fumigant formulations to contaminate groundwater in vulnerable aquifers.

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37

Bopp, Richard F., Steven N. Chillrud, Edward L. Shuster, H. James Simpson, and Frank D. Estabrooks. "Trends in Chlorinated Hydrocarbon Levels in Hudson River Basin Sediments." Environmental Health Perspectives 106 (August 1998): 1075. http://dx.doi.org/10.2307/3434155.

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38

KUCHIDA, Keigo, Shinji SATO, Masamichi SEINO, Katsumi TAMAKAWA, Takeo KATO, and Masahiko OBA. "Investigation of the Volatile Chlorinated Hydrocarbon Concentrations around Emission Sources." Journal of Environmental Chemistry 5, no. 3 (1995): 683–88. http://dx.doi.org/10.5985/jec.5.683.

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39

Bourg, Alain C. M., Philippe Degranges, Christophe Mouvet, and Jean Pierre Sauty. "Migration of chlorinated hydrocarbon solvents through Coventry sandstone rock columns." Journal of Hydrology 149, no. 1-4 (August 1993): 183–207. http://dx.doi.org/10.1016/0022-1694(93)90106-j.

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40

Milanovich, F. P., S. B. Brown, B. W. Colston Jr., P. F. Daley, and K. C. Langry. "A fiber-optic sensor system for monitoring chlorinated hydrocarbon pollutants." Talanta 41, no. 12 (December 1994): 2189–94. http://dx.doi.org/10.1016/0039-9140(94)00159-6.

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41

Bopp, R. F., S. N. Chillrud, E. L. Shuster, H. J. Simpson, and F. D. Estabrooks. "Trends in chlorinated hydrocarbon levels in Hudson River basin sediments." Environmental Health Perspectives 106, suppl 4 (August 1998): 1075–81. http://dx.doi.org/10.1289/ehp.98106s41075.

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42

McNab, Walt W., David W. Rice, and Cary Tuckfield. "Evaluating Chlorinated Hydrocarbon Plume Behavior Using Historical Case Population Analyses." Bioremediation Journal 4, no. 4 (October 2000): 311–35. http://dx.doi.org/10.1080/10889860091114284.

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43

Wang, Yi. "Chlorinated Hydrocarbon-Contaminated Site Investigation With Optimized 3D-CSIA Approach." Remediation Journal 23, no. 2 (March 2013): 111–20. http://dx.doi.org/10.1002/rem.21351.

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44

Carlson, Lars A., and Birgitta Kolmodin-Hedman. "HYPER-α-LIPOPROTEINEMIA IN MEN EXPOSED TO CHLORINATED HYDROCARBON PESTICIDES." Acta Medica Scandinavica 192, no. 1-6 (April 24, 2009): 29–32. http://dx.doi.org/10.1111/j.0954-6820.1972.tb04773.x.

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45

Frangos, Stephen A., and John M. Peters. "Re: Chlorinated hydrocarbon solvents: Substituting our way toward human carcinogenicity." American Journal of Industrial Medicine 27, no. 3 (March 1995): 447–48. http://dx.doi.org/10.1002/ajim.4700270315.

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46

Doyle, E. A., and G. F. Fries. "Induction of aryl hydrocarbon hydroxylase by chlorinated dibenzofurans in rats." Chemosphere 15, no. 9-12 (January 1986): 1745–48. http://dx.doi.org/10.1016/0045-6535(86)90462-5.

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47

Needham, L. L., V. W. Burse, S. L. Head, M. P. Korver, P. C. McClure, J. S. Andrews, D. L. Rowley, J. Sung, and S. E. Kahn. "Adipose tissue/serum partitioning of chlorinated hydrocarbon pesticides in humans." Chemosphere 20, no. 7-9 (January 1990): 975–80. http://dx.doi.org/10.1016/0045-6535(90)90208-b.

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48

Westernhagen, H. Von, P. Cameron, D. Janssen, and M. Kerstan. "Age and size dependent chlorinated hydrocarbon concentrations in marine teleosts." Marine Pollution Bulletin 30, no. 10 (October 1995): 655–59. http://dx.doi.org/10.1016/0025-326x(95)00040-t.

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49

Zhao, Xianda, Roger B. Wallace, David W. Hyndman, Michael J. Dybas, and Thomas C. Voice. "Heterogeneity of chlorinated hydrocarbon sorption properties in a sandy aquifer." Journal of Contaminant Hydrology 78, no. 4 (August 2005): 327–42. http://dx.doi.org/10.1016/j.jconhyd.2005.06.002.

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50

Nissen, Silke, Bruce D. Alexander, Ilyas Dawood, Martin Tillotson, Richard P. K. Wells, Donald E. Macphee, and Kenneth Killham. "Remediation of a chlorinated aromatic hydrocarbon in water by photoelectrocatalysis." Environmental Pollution 157, no. 1 (January 2009): 72–76. http://dx.doi.org/10.1016/j.envpol.2008.07.024.

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