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Paraffin effects

US EPA (1985) Risk Assessment for chlorinated paraffins Effect on fish and wildlife. Environmental Protection Agency, Health and Environmental Review Division, Toxicology Section, Washington DC, Dec. 18,1985... [Pg.165]

Paraffin effective activation energy plofs for the PtHZSM-5 catalyst reflect the bimodal nature of the evolution profiles The increase in activation energy may be due to increased steric hindrance for cracking reactions that take place within HZSM-5 channels. [Pg.66]

The solubility of hydrocarbon liquids from the same chemical family diminishes as the molecular weight increases. This effect is particularly sensitive thus in the paraffin series, the solubility expressed in mole fraction is divided by a factor of about five when the number of carbon atoms is increased by one. The result is that heavy paraffin solubilities are extremely small. The polynuclear aromatics have high solubilities in water which makes it difficult to eliminate them by steam stripping. [Pg.168]

The varying actual orientation of molecules adsorbed at an aqueous solution-CCU interface with decreasing A has been followed by resonance Raman spectroscopy using polarized light [130]. The effect of pressure has been studied for fatty alcohols at the water-hexane [131] and water-paraffin oil [132] interfaces. [Pg.85]

Each olefin is more soluble than the paraffin of the same chain length, but the solubiHty of both species declines as chain length increases. Thus, in a broa d-boiling mixture, solubiHties of paraffins and olefins overlap and separation becomes impossible. In contrast, the relative adsorption of olefins and paraffins from the Hquid phase on the adsorbent used commercially for this operation is shown in Figure 2. Not only is there selectivity between an olefin and paraffin of the same chain length, but also chain length has Httie effect on selectivity. Consequentiy, the complete separation of olefins from paraffins becomes possible. [Pg.291]

Zinc Sta.nna.tes, The zinc staimates are also effective synergists for flexible PVC however, as shown in Figure 4a, antimony oxide is more effective. If more chlorine such as in a chlorinated paraffin such as Cereclor is added, then the staimates become more effective and eventually outperform antimony oxide (Fig. 4b). [Pg.460]

Olefins, Diolefins, and Acetylenes. Members of this category having up to four carbon atoms are both asphyxiants and anesthetics, and potency for the latter effect increases with carbon chain length. Skin-contact effects are similar to those of paraffins. [Pg.370]

Gycloparaffins. Members of this class produce effects much like the paraffins, except that unsaturated cycloparaffins are more noxious than the saturated counterparts. Breathing high concentrations of cycloparaffin vapors can result in irritation and anesthesia. [Pg.370]

Pour-Point Depressants. The pour point of alow viscosity paraffinic oil may be lowered by as much as 30—40°C by adding 1.0% or less of polymethacrylates, polymers formed by Eriedel-Crafts condensation of wax with alkylnaphthalene or phenols, or styrene esters (22). As wax crystallizes out of solution from the Hquid oil as it cools below its normal pour point, the additive molecules appear to adsorb on crystal faces so as to prevent growth of an interlocking wax network which would otherwise immobilize the oil. Pour-point depressants become less effective with nonparaffinic and higher viscosity petroleum oils where high viscosity plays a dominant role in immobilizing the oil in a pour-point test. [Pg.242]

Dry lubricants are usually added to the powder in order to decrease the friction effects. The more common lubricants include zinc stearate [557-05-17, lithium stearate [4485-12-5] calcium stearate [1592-23-0] stearic acid [57-11-4] paraffin, graphite, and molybdenum disulfide [1317-33-5]. Lubricants are generally added to the powder in a dry state in amounts of 0.25—1.0 wt % of the metal powder. Some lubricants are added by drying and screening a slurry of powder and lubricant. In some instances, lubricants are appHed in Hquid form to the die wall. [Pg.185]

Toxicological Information. The toxicity of the higher olefins is considered to be virtually the same as that of the homologous paraffin compounds. Based on this analogy, the suggested maximum allowable concentration in air is 500 ppm. Animal toxicity studies for hexene, octene, decene, and dodecene have shown Httle or no toxic effect except under severe inhalation conditions. The inhalation LD q for 1-hexene is 33,400 ppm for these olefins both LD q (oral) and LD q (dermal) are >10 g/kg. [Pg.442]

Evaporation Retardants. Small molecule solvents that make up the most effective paint removers also have high vapor pressure and evaporate easily, sometimes before the remover has time to penetrate the finish. Low vapor pressure cosolvents are added to help reduce evaporation. The best approach has been to add a low melting point paraffin wax (mp = 46-57° C) to the paint remover formulation. When evaporation occurs the solvent is chilled and the wax is shocked-out forming a film on the surface of the remover that acts as a barrier to evaporation (5,6). The addition of certain esters enhances the effectiveness of the wax film. It is important not to break the wax film with excessive bmshing or scraping until the remover has penetrated and lifted the finish from the substrate. Likewise, it is important that the remover be used at warm temperatures, since at cool temperatures the wax film may not form, or if it does it will be brittle and fracture. Rapid evaporation occurs when the wax film is absent or broken. [Pg.550]

In petroleum and oxygenate finish removers, the major ingredient is normally acetone, methyl ethyl ketone [78-93-3], or toluene. Cosolvents include methanol, / -butanol [71-36-3], j -butyl alcohol [78-92-2], or xylene [1330-20-7]. Sodium hydroxide or amines are used to activate the remover. Paraffin wax is used as an evaporation retarder though its effectiveness is limited because it is highly soluble in the petroleum solvents. CeUulose thickeners are sometimes added to liquid formulas to assist in pulling the paraffin wax from the liquid to form a vapor barrier or to make a thick formula. Corrosion inhibitors are added to stabili2e tbe formula for packaging (qv). [Pg.551]

Paraffin wax additives are effective in overcoming surface inhibition by forming a monomolecular wax layer at the curing surface. Although effective in excluding oxygen, this waxy layer must be removed for subsequent lamination or bonding processes (see Waxes). [Pg.320]

HP Alkylation Process. The most widely used technology today is based on the HE catalyst system. AH industrial units built in the free world since 1970 employ this process (78). During the mid-1960s, commercial processes were developed to selectively dehydrogenate linear paraffins to linear internal olefins (79—81). Although these linear internal olefins are of lower purity than are a olefins, they are more cost-effective because they cost less to produce. Furthermore, with improvement over the years in dehydrogenation catalysts and processes, such as selective hydrogenation of diolefins to monoolefins (82,83), the quaUty of linear internal olefins has improved. [Pg.51]


See other pages where Paraffin effects is mentioned: [Pg.222]    [Pg.295]    [Pg.222]    [Pg.295]    [Pg.206]    [Pg.208]    [Pg.217]    [Pg.353]    [Pg.443]    [Pg.2789]    [Pg.2790]    [Pg.138]    [Pg.255]    [Pg.292]    [Pg.456]    [Pg.458]    [Pg.164]    [Pg.220]    [Pg.81]    [Pg.193]    [Pg.193]    [Pg.264]    [Pg.198]    [Pg.241]    [Pg.449]    [Pg.377]    [Pg.95]    [Pg.102]    [Pg.103]    [Pg.311]    [Pg.316]    [Pg.317]    [Pg.237]    [Pg.238]   
See also in sourсe #XX -- [ Pg.249 ]




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Model paraffins, effects

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