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Poly aromatization

Another application of SFC-GC was for the isolation of chrysene, a poly aromatic hydrocarbon, from a complex liquid hydrocarbon industrial sample (24). A 5 p.m octadecyl column (200 cm X 4.6 mm i.d.) was used for the preseparation, followed by GC analysis on an SE-54 column (25 m X 0.2 mm i.d., 0.33 p.m film thickness). The direct analysis of whole samples transferred from the supercritical fluid chromatograph and selective and multi-heart-cutting of a particular region as it elutes from the SFC system was demonstrated. The heart-cutting technique allows the possibility of separating a trace component from a complex mixture (Figure 12.21). [Pg.327]

An alternative approach utilizes polymeric analogs of PBD. The oxadiazole unit may be in the polymer main chain or attached as a side chain. A reasonable device performance has been demonstrated in poly(aromatic oxadia/ole)s [71—74. ... [Pg.338]

Allied to flammability is smoke density suppression especially in confined spaces, e.g., airliners, houses, warehouses. Many aromatic compounds bum with a smoky flame (e.g., styrene), whereas corresponding aliphatic compounds tend to burn with a clean "transparent" flame. This is because air-bome poly-aromatic vapours decompose to give volatile carbon (smoke) in low oxygen environments. [Pg.109]

Schnaak et al. [4] Polychlorinated terphenyls, naphthalenes, chloropesticides, halogenated hydrocarbon solvents, aromatic hydrocarbon solvents (BTEX), chlorobenzenes, poly aromatic hydrocarbons (EPA 610), phenols, chlorophenols, phthalates, petroleum hydrocarbons, LAS and nonylphenol (NP), organotin compounds and 2,4-dichloroaniline 1 pg/kg to 10 mg/kg for chlorine-contained compounds 10 pg/kg to 1 g/kg for solvent and phenols 1 mg/kg to 10 g/kg for EPA610, DEHP, LAS, and mineral oils Sewage sludge... [Pg.117]

The benefits related to the particular topology of ITQ-21 when used as heterogeneous catalyst have been reported for different processes, such as catalytic cracking [1], hydrocracking [2] or hidrogenation and ring opening of (poly)aromatics [3]... [Pg.333]

Lochmuller and coworkers used the formation of excimer species to answer a distance between site question related to the organization and distribution of molecules bound to the surface of silica xerogels such as those used for chromatography bound phases. Pyrene is a flat, poly aromatic molecule whose excited state is more pi-acidic than the ground state. An excited state of pyrene that can approach a ground state pyrene within 7A will form an excimer Pyr +Pyr (Pyr)2. Monomer pyrene emits at a wavelength shorter than the excimer and so isolated versus near-neighbor estimates can be made. In order to do this quantitatively, these researchers turned to measure lifetime because the monomer and excimer are known to have different lifetimes in solution. This is also a way to introduce the concept of excited state lifetime. [Pg.262]

Aromatic hydrocarbons The inner circle indicates the conjugated molecular orbital. Many rings may be fused together to create PAHs (poly aromatic hydrocarbons) Phenyl -/-benzene 0 Usually the aromatic rings are written together e.g., for benzene C6H6... [Pg.270]

Janini, GM., Johnston, K., and Zielinski, W.L., Use of a nematic liquid-crystal for gas-liquid-chromatographic separation of poly aromatic hydrocarbons, Anal Chem., 47, 670, 1975. [Pg.291]

The soil-cement mixing wall (SMW) is an in situ technology for the fixation, stabilization, and solidification of soils contaminated with metals and semivolatile organic compounds. SMW can be used to treat soils contaminated with pesticides, polychlorinated biphenyls (PCBs), phenols, and poly aromatic hydrocarbons (PAHs) to depths of up to 100 ft. The technology uses hollow-stem augers to inject solidification/stabilization agents and blend them with the soil. [Pg.941]

Pollutants derived from nonpoint sources run-off from agricultural lands (fertilizers, pesticides, humic materials), run-off from urban areas (salt, poly aromatic hydrocarbons [PAHs], asbestos), atmospheric fallout (particulates containing sulfate, nitrate, heavy metals, PAHs, and chlorinated organics). [Pg.714]


See other pages where Poly aromatization is mentioned: [Pg.503]    [Pg.261]    [Pg.84]    [Pg.233]    [Pg.17]    [Pg.57]    [Pg.405]    [Pg.292]    [Pg.292]    [Pg.113]    [Pg.63]    [Pg.518]    [Pg.41]    [Pg.25]    [Pg.64]    [Pg.449]    [Pg.349]    [Pg.357]    [Pg.365]    [Pg.367]    [Pg.371]    [Pg.375]    [Pg.385]    [Pg.395]    [Pg.399]    [Pg.401]    [Pg.409]    [Pg.417]    [Pg.425]    [Pg.429]    [Pg.439]    [Pg.445]    [Pg.449]    [Pg.453]    [Pg.457]    [Pg.459]    [Pg.469]    [Pg.30]    [Pg.261]    [Pg.353]   
See also in sourсe #XX -- [ Pg.449 ]




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Aromatic Polysulfides Poly(arylene Sulfide)s

Aromatic diacids, poly

Aromatic poly

Aromatic poly

Aromatic poly alkane

Aromatic poly anhydrides

Aromatic poly imines

Aromatic poly sulfonates

Aromatic poly synthesis

Aromatic poly(ether sulfone)

Aromatic polyamides Poly

OTHER POLY(AROMATIC AMINES)

Partially Aromatic Poly(amide)s

Phosphorus-containing aromatic poly

Poly , aromatic synthesis procedure

Poly aromatic dioxygenase

Poly aromatic hydrocarbon formation

Poly aromatic polymer

Poly aromatics

Poly aromatics

Poly aromatics Wittig reaction

Poly aromatics ethylene oxide

Poly aromatics pyrrole

Poly aromatics radicals

Poly aromatics ring opening

Poly aromatics thermal decomposition

Poly aromatics transesterification

Poly halogenated aromatic hydrocarbons

Poly high-temperature aromatic polymer

Poly polarizable aromatic groups

Poly(alkyl and aromatic ethers)

Poly(methacrylate)s Containing Aromatic Side Chains

Poly-aromatic hydrocarbons

Thermotropic aromatic poly

Thermotropic aromatic poly ester-amides)

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