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Fluorine nitrogen

Fig. 5. Equipment foi surface treating plastic components. Parts ate loaded into one of the two lower chambers which is then evacuated to remove most of the air. This chamber is then flooded with a dilute mixture of fluorine and nitrogen which is made and stored in the upper chamber. After the treatment is completed, the fluorine mixture is pumped back up to the upper chamber for storage and the lower chamber repeatedly flooded with air and evacuated to remove any traces of fluorine gas. Two treatment chambers are cycled between the loading/unloading operation and the treatment step to increase equipment output. The fluorine—nitrogen blend may be used several times before by-products from the treatment process begin to interfere. AH waste... Fig. 5. Equipment foi surface treating plastic components. Parts ate loaded into one of the two lower chambers which is then evacuated to remove most of the air. This chamber is then flooded with a dilute mixture of fluorine and nitrogen which is made and stored in the upper chamber. After the treatment is completed, the fluorine mixture is pumped back up to the upper chamber for storage and the lower chamber repeatedly flooded with air and evacuated to remove any traces of fluorine gas. Two treatment chambers are cycled between the loading/unloading operation and the treatment step to increase equipment output. The fluorine—nitrogen blend may be used several times before by-products from the treatment process begin to interfere. AH waste...
MISCELLANEOUS FLUORINATED NITROGEN HETEROGYGLIGS Two reviews (1981, 1990) include nitrogen heterocychcs not covered in the present survey (482,483). The 1990 review dealing with four-, five-, and six-membered ring heterocycHc compounds emphasizes biological properties (482). [Pg.340]

The Air Force Dispersion Assessment Model (ADAM -1980s) calculates the source term and dispersion of accidental releases of eight specific chemicals chlorine, fluorine, nitrogen tetroji ogen sulfide, hydrogen fluoride, sulfur dioxide, phosgene, and ammonia. It Ut a ... [Pg.347]

Fluorine Nitrogenous bases Trifluoromethyl hypofluorite Pyridine See other organic bases... [Pg.606]

Fluorine nitrate Organic materials Fluorine Nitrogenous bases... [Pg.778]

However, the fact that industrial applications of polymer surface fluorination employ a fluorine/nitrogen mixture as the fluorinating agent complicates matters because fluorine gas is toxic, may explode when brought into contact with organic substances, and causes severe bums on human tissue. Moreover, the use of fluorine requires highly qualified personnel and special safety systems. [Pg.224]

Treatment with fluorine/nitrogen mixtures (fluorination) increases the polar component of the surface energy initially, but longer treatment times result in a drop in both the polar component and the total surface energy24 25 (see Figure 16.3). At very long treatment times the surface energy ofthe treated surface can be lower than that of the polyolefin itself. [Pg.248]

NMR is an extremely powerful method for observing the environment of an atom of interest. The element most commonly studied is hydrogen bonded to another element, usually carbon, and is referred to as NMR spectroscopy (sometimes called HNMR, H NMR, P NMR, or proton NMR). The second most commonly studied element is carbon, specifically 13C, bonded to other carbon atoms and to hydrogen atoms. Other elements commonly measured include fluorine, nitrogen, and phosphorus. [Pg.303]

Fluorine is the most energetic oxidizing element and as such is of prime importance in advanced oxidizers. The fluorine-based oxidizers discussed here include elemental fluorine, compounds containing oxygen and fluorine, nitrogen-fluorine compounds, halogen fluorides, and noble gas fluorides. [Pg.337]

Miller. Calfee and Bigelow made 1,1,2,2-tetrachlorodifluorOethane from a vapor-phase reaction of fluorine/nitrogen mixtures with hexachloroethane or tetrachlorocthene over copper gauze. Calfee and Bigelow fluorinated ethane likewise, obtaining hexafluoroethane and carbon tetrafluoride. [Pg.9]

Young, Fukuhara and Bigelow repeated the vapor-phase reaction of fluorine/nitrogen mixtures with ethane, obtaining pentafluoroethane. 1,1.2,2-tetrafluoroethane. and 1,1,2-tri-fluoroethane, together with products of C — C bond fission. [Pg.9]

Hadley and Bigelow fluorinated methane with fluorine/nitrogen mixtures in the vapor phase over copper gauze. All four fluoromethanes were obtained, together with hexafluoroethane and octafluoropropane. As an explanation, the first specific free-radical chain mechanism to be published for a fluorination process was invoked. [Pg.9]

The contribution of structure III would be expected to amount to a few percent for BrNO and C1NO, and much more for FNO, because of the greater stability of the fluorine-nitrogen double covalent bond. A resonating structure with 50 percent contribution of II, 25 percent of I, and 25 percent of III is compatible with both the observed F—N distance in FNO and the observed value18 1.81 D of the electric dipole moment. [Pg.346]

Methane Oxygen Fluorine Nitrogen Hydrogen Helium... [Pg.230]


See other pages where Fluorine nitrogen is mentioned: [Pg.131]    [Pg.335]    [Pg.295]    [Pg.70]    [Pg.738]    [Pg.599]    [Pg.161]    [Pg.354]    [Pg.43]    [Pg.281]    [Pg.23]    [Pg.17]    [Pg.109]    [Pg.205]    [Pg.670]    [Pg.343]    [Pg.285]    [Pg.70]    [Pg.1188]    [Pg.130]    [Pg.392]    [Pg.2577]    [Pg.22]    [Pg.39]    [Pg.347]    [Pg.173]    [Pg.335]    [Pg.319]   
See also in sourсe #XX -- [ Pg.12 ]




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