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- Naphthalene - an overview | ScienceDirect Topics
Naphthalene (91-20-3) is a component of crude oil and is found in petroleum-derived fuels and consumer products The most common use of naphthalene in consumer products is in the production of mothballs Naphthalene ingestion can result in acute as well as delayed toxicity The primary target organs of toxicity are the blood and the eyes
- Naphthalene, a versatile platform in medicinal chemistry: Sky-high . . .
Naphthalene, the simplest bicyclic aromatic ring, is conventionally derived from coal tar It is a white solid material with strong pungent odour Naphthalene was first discovered by Scottish chemist, Alexzander garden in 1819 Michael Faraday first reported its molecular formula (C 10 H 8) in 1826 [1] Conventionally, naphthalene is
- Naphthalene - an overview | ScienceDirect Topics
Naphthalene conversion (naphthalene hydrogenated to tetralin, octalins and decalins) varied from 4 to 96% This corresponds to a naphthalene hydrogenation rate of 1-24×10 3 mol (kg cat s) An additional experiment carried out with very low catalyst loading led to a low naphthalene conversion and only tetralin as product
- Naphthalene - an overview | ScienceDirect Topics
Naphthalene (91-20-3) is a component of crude oil and is found in petroleum-derived fuels and consumer products The most common use of naphthalene in consumer products is in the production of mothballs Naphthalene ingestion can result in acute as well as delayed toxicity The primary target organs of toxicity are the blood and the eyes
- Naphthalene: Risk assessment and environmental health hazard
Naphthalene is a two fused benzene ring polycyclic aromatic hydrocarbon Naphthalene was initially registered with the U S Department of Agriculture (USDA) as a pesticide in 1948 The United States Environmental Protection Agency (EPA) issued a registration standard for naphthalene in 1981, and the substance was reregistered by the agency in 2008
- Naphthalene - an overview | ScienceDirect Topics
Naphthalene Naphthalene is the most volatile polyaromatic hydrocarbon The migration of its vapors from creosote-contaminated groundwater to surface soil poses a risk at the former railroad tie operation site at Oneida, Tennessee [21]
- Unraveling the atmospheric oxidation mechanism and kinetics of . . .
Naphthalene, the most abundant polycyclic aromatic hydrocarbon in the atmosphere, significantly influences OH consumption and secondary organic aerosol (SOA) formation Naphthoquinone (NQ) is a significant contributor to ring-retaining SOA from naphthalene degradation, impacting the redox properties and toxicity of ambient particles
- Mechanism for the catalytic thermal polycondensation of naphthalene at . . .
Compared with naphthalene and 1,1'-binaphthalene, the naphthalene polymers N-10-150-0 5 and N-10-150-8 display obviously weaker peaks at 781 cm–1, indicating that the proportion of naphthalene rings in the naphthalene polymer is greatly reduced and the PAHs with higher degree of aromatization are formed
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