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List Of Superfund Sites In Texas
This is a list of Superfund sites in Texas designated under the Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA) environmental law. The CERCLA federal law of 1980 authorized the United States Environmental Protection Agency (EPA) to create a list of polluted locations requiring a long-term response to clean up hazardous material contaminations. These locations are known as Superfund sites, and are placed on the National Priorities List (NPL). The NPL guides the EPA in "determining which sites warrant further investigation" for environmental remediation. As of September 6, 2017, there are 53 Superfund sites on the National Priorities List in Texas. One new site has been proposed for inclusion on the list. Twelve additional sites have been cleaned up and are considered deleted, with no further action required. One NPL site included in this list, Motco, Inc., has been designated as the state's Top Priority Site. According to CERCLA, states may make ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
United States Environmental Protection Agency
The Environmental Protection Agency (EPA) is an independent executive agency of the United States federal government tasked with environmental protection matters. President Richard Nixon proposed the establishment of EPA on July 9, 1970; it began operation on December 2, 1970, after Nixon signed an executive order. The order establishing the EPA was ratified by committee hearings in the House and Senate. The agency is led by its administrator, who is appointed by the president and approved by the Senate. The current administrator is Michael S. Regan. The EPA is not a Cabinet department, but the administrator is normally given cabinet rank. The EPA has its headquarters in Washington, D.C., regional offices for each of the agency's ten regions and 27 laboratories. The agency conducts environmental assessment, research, and education. It has the responsibility of maintaining and enforcing national standards under a variety of environmental laws, in consultation with sta ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Phenanthrene
Phenanthrene is a polycyclic aromatic hydrocarbon (PAH) with formula C14H10, consisting of three fused benzene rings. It is a colorless, crystal-like solid, but can also appear yellow. Phenanthrene is used to make dyes, plastics and pesticides, explosives and drugs. It has also been used to make bile acids, cholesterol and steroids. Phenanthrene occurs naturally and also is a man-made chemical. Commonly, humans are exposed to phenanthrene through inhalation of cigarette smoke but there are many routes of exposure. Animal studies have shown that phenanthrene is a potential carcinogen. However, according to IARC, it is not identified as a probable, possible or confirmed human carcinogen. Phenanthrene's three fused rings are angled as in the phenacenes, rather than straight as in the acenes. The compound with a phenanthrene skeleton and nitrogens at the 4 and 5 positions is known as phenanthroline. Chemistry Phenanthrene is nearly insoluble in water but is soluble in most low po ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Vinyl Chloride
Vinyl chloride is an organochloride with the formula H2C=CHCl. It is also called vinyl chloride monomer (VCM) or chloroethene. This colorless compound is an important industrial chemical chiefly used to produce the polymer polyvinyl chloride (PVC). About 13 million metric tonne are produced annually. VCM is among the top twenty largest petrochemicals (petroleum-derived chemicals) in world production. The United States currently remains the largest VCM manufacturing region because of its low-production-cost position in chlorine and ethylene raw materials. China is also a large manufacturer and one of the largest consumers of VCM. Vinyl chloride is a gas with a sweet odor. It is highly toxic, flammable, and carcinogenic. It can be formed in the environment when soil organisms break down chlorinated solvents. Vinyl chloride that is released by industries or formed by the breakdown of other chlorinated chemicals can enter the air and drinking water supplies. Vinyl chloride is a common ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
1,1-dichloroethene
1,1-Dichloroethene, commonly called 1,1-dichloroethylene or vinylidene chloride or 1,1-DCE, is an organochloride with the molecular formula CHCl. It is a colorless liquid with a sharp odor. Like most chlorocarbons, it is poorly soluble in water, but soluble in organic solvents. 1,1-DCE was the precursor to the original clingwrap, Saran, for food, but this application has been phased out. Production 1,1-DCE is produced by dehydrochlorination of 1,1,2-trichloroethane, a relatively unwanted byproduct in the production of 1,1,1-trichloroethane and 1,2-dichloroethane. The conversion is a base-catalyzed reaction which uses either NaOH or Ca(OH) with temperature ca. 100 °C. :ClCHCHCl + NaOH → ClC=CH + NaCl + HO The gas phase reaction, without the base, would be more desirable but is less selective. Applications 1,1-DCE is mainly used as a comonomer in the polymerization of vinyl chloride, acrylonitrile, and acrylates. It is also used in semiconductor device fabri ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
1,2-dichloroethane
The chemical compound 1,2-dichloroethane, commonly known as ethylene dichloride (EDC), is a chlorinated hydrocarbon. It is a colourless liquid with a chloroform-like odour. The most common use of 1,2-dichloroethane is in the production of vinyl chloride, which is used to make polyvinyl chloride (PVC) pipes, furniture and automobile upholstery, wall coverings, housewares, and automobile parts. 1,2-Dichloroethane is also used generally as an intermediate for other organic chemical compounds, and as a solvent. It forms azeotropes with many other solvents, including water (at a boiling point of ) and other chlorocarbons. History In 1794, physician Jan Rudolph Deiman, merchant Adriaan Paets van Troostwijk, chemist Anthoni Lauwerenburg, and botanist Nicolaas Bondt, under the name of Society of Dutch Chemists ( nl, Gezelschap der Hollandsche Scheikundigen), were the first to produce 1,2-dichloroethane from olefiant gas (oil-making gas, ethylene) and chlorine gas. Although ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
1,1-dichloroethane
1,1-Dichloroethane is a chlorinated hydrocarbon. It is a colorless oily liquid with a chloroform-like odor. It is not easily soluble in water, but miscible with most organic solvents. Large volumes of 1,1-dichloroethane are manufactured, with annual production exceeding 1 million pounds in the United States. It is mainly used as a feedstock in chemical synthesis, chiefly of 1,1,1-trichloroethane. It is also used as a solvent for plastics, oils and fats, as a degreaser, as a fumigant in insecticide sprays, in halon fire extinguishers, and in cementing of rubber. It is used in manufacturing of high-vacuum resistant rubber and for extraction of temperature-sensitive substances. Thermal cracking at 400–500 °C and 10 MPa yields vinyl chloride. In the past, 1,1-dichloroethane was used as a surgical inhalational anesthetic. Safety 1,1-dichloroethane has been on the California Proposition 65 list of known carcinogens since 1990. In the atmosphere, 1,1-dichloroethane de ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
1,2-dichloroethene
1,2-Dichloroethene, commonly called 1,2-dichloroethylene or 1,2-DCE, is the name for a pair of organochlorine compounds with the molecular formula CHCl. They are both colorless liquids with a sweet odor. It can exist as either of two geometric isomers, ''cis''-1,2-dichloroethene or ''trans''-1,2-dichloroethene, but is often used as a mixture of the two. They have modest solubility in water. These compounds have some applications as a degreasing solvent. In contrast to most ''cis-trans'' compounds, the ''Z'' isomer (''cis'') is more stable than the ''E'' isomer (''trans'') by 0.4 kcal/mol. Production and use ''cis''-DCE, the ''Z'' isomer, is obtainable by the controlled chlorination of acetylene: :CH + Cl → CHCl Industrially both isomers arise as byproducts of the production of vinyl chloride, which is produced on a vast scale. Unlike vinyl chloride, the 1,2-dichloroethylene isomers do not polymerize. ''trans''-DCE has applications including electronics cleaning, ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
1,1,2-trichloroethane
1,1,2-Trichloroethane, or 1,1,2-TCA, is an organochloride solvent with the molecular formula CHCl. It is a colourless, sweet-smelling liquid that does not dissolve in water, but is soluble in most organic solvent A solvent (s) (from the Latin '' solvō'', "loosen, untie, solve") is a substance that dissolves a solute, resulting in a solution. A solvent is usually a liquid but can also be a solid, a gas, or a supercritical fluid. Water is a solvent for ...s. It is an isomer of 1,1,1-Trichloroethane, 1,1,1-trichloroethane. It is used as a solvent and as an intermediate in the synthesis of 1,1-Dichloroethane, 1,1-dichloroethane. 1,1,2-TCA is a central nervous system depressant and inhalation of vapors may cause dizziness, drowsiness, headache, nausea, shortness of breath, and unconsciousness. Toxicology Trichloroethane may be harmful by inhalation, ingestion, and skin contact. It is a respiratory and eye irritant. Although no definitive studies currently exist, trichloroe ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Volatile Organic Compound
Volatile organic compounds (VOCs) are organic compounds that have a high vapour pressure at room temperature. High vapor pressure correlates with a low boiling point, which relates to the number of the sample's molecules in the surrounding air, a trait known as volatility. VOCs are responsible for the odor of scents and perfumes as well as pollutants. VOCs play an important role in communication between animals and plants, e.g. attractants for pollinators, protection from predation, and even inter-plant interactions. Some VOCs are dangerous to human health or cause harm to the environment. Anthropogenic VOCs are regulated by law, especially indoors, where concentrations are the highest. Most VOCs are not acutely toxic, but may have long-term chronic health effects. Definitions Diverse definitions of the term VOC are in use. Canada Health Canada classifies VOCs as organic compounds that have boiling points roughly in the range of . The emphasis is placed on commonly encountere ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Harris County, Texas
Harris County is a county located in the U.S. state of Texas; as of the 2020 census, the population was 4,731,145, making it the most populous county in Texas and the third most populous county in the United States. Its county seat is Houston, the largest city in Texas and fourth largest city in the United States. The county was founded in 1836 and organized in 1837. It is named for John Richardson Harris, who founded the town of Harrisburg on Buffalo Bayou in 1826. According to the July 2021 census estimate, Harris County's population has shifted to 4,728,030 comprising over 16% of Texas's population. Harris County is included in the nine-county Houston–The Woodlands–Sugar Land metropolitan statistical area, which is the fifth-most populous metropolitan area in the United States. History Human remains date habitation to about 4000 BC. Other evidence of humans in the area dates from about 1400 BC, 1 AD, and later in the first millennium. The region became uninhabi ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Brio Superfund Site
The Brio Superfund site is a former industrial location in Harris County, Texas at the intersection of Beamer Road and Dixie Farm Road, about southeast of downtown Houston, and adjacent to the Dixie Oil Processors Superfund site. It is a federal Superfund site, although it was deleted from the National Priorities List in December 2006. A neighboring residential subdivision called South Bend, now abandoned, was located along and north of the northern boundary of Brio North. The former South Bend neighborhood consisted of about 670 homes, an elementary school, and a Little League baseball field. Documents pertaining to the Brio Superfund site are located at the San Jacinto College South Campus Library, which houses Brio Site Repository Documents, U.S. Environmental Protection Agency (EPA) Administrative Records, and documents concerning the adjoining Dixie Oil Processors site. Site history and contamination The 58-acre Brio Refinery site was home to several chemical companies bet ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
