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Volatility level

When additional lubricants, eg, mineral oil and butyl stearate, are added to PS, easy-flow materials are produced. Improved flow is usually achieved at the cost of lowering the heat-deformation temperature. Stiff-flow PS has a high molecular weight and a low volatile level and is useful for extmsion apphcations. Typical levels of residuals in PS grades are Hsted in Table 2. Differences in molecular weight distribution are illustrated in Figure 4. [Pg.505]

The plate dryer is limited in its scope of apphcations only in the consistency of the feed material (the products must be friable, free flowing, and not undergo phase changes) and diying temperatures up to 320°C. Applications include speci ty chemicals, pharmaceuticals, foods, polymers, pigments, etc. Initial moisture or volatile level can be as high as 65 percent and the unit is often used as a final dryer to take materials to a bone-dry state, if necessary. The plate dryer can also be used for heat treatment, removal of waters of hydration (bound moisture), solvent removal, and as a product cooler. [Pg.1216]

The first two impregnation methods clearly dominate in North America and, probably, most of the world, whereas injection pultrusion is favored in several European countries where the permissible volatile levels in the workplace tend to be the lowest. Although injection pultrusion may be the simplest way of solving the monomer emission problem, it is clearly possible to reduce this disadvantage of the first two impregnation methods through proper ventilation. [Pg.321]

As volatile levels drop further, yielding very concentrated polymer solutions, the viscosity increases to a level that requires rotary equipment for forward pumping of the solution, which imparts surface renewal and often entraps vapor bubbles, for improved mass and heat transfer as well. There is a wide variety of rotary equipment available, from advanced ribbon devolatilizers, vertical-cone devolatilizers, and disk-ring devolatilizers for moderately viscous solutions, to single and twin screw devolatilizers and thin-film... [Pg.411]

Yet in spite of all the evidence just presented, it is not impossible that at very low volatile levels the Latinen-type model may have some validity, but this likelihood appears to be small because foaming was observed at volatile concentrations as low as 50 ppm. Moreover, the likelihood further diminishes due to the fact that, as shown in Section 8.5, the diffusivity of small molecules in polymeric melts may drop by orders of magnitude, with dropping concentrations at these levels. [Pg.416]

A micro version of the distillation extraction apparatus has been described by Godefroot t al, (2J). This apparatus uses heavier than water solvents, e.g., methylene chloride or carbon disulfide as the extractant. Because only one milliliter of solvent is used, no further concentration of solvent is required. The authors found 15 minutes distillation/extraction time sufficient for recovery of nonpolar compounds, e.g., mono and sesquiterpenes, while one hour was required for oxygenated and higher boiling compounds. This apparatus was evaluated by Nunez and Bemelmans (28) for low levels of aroma compounds in water. They reported that results were satisfactory for volatile levels greater than 1 ppm. [Pg.47]

Low molecular weight PVC homopolymer is made at higher reaction temperature. Generally less initiator, usually lauroyl peroxide or azobisisobutyronitrile (AIBN) is needed, and there is improved heat removal capacity because of the increased differential with the cooling water. Low molecular weight polymers are more difficult to strip of residual VCM and to dry down to low volatile levels. [Pg.395]

Batch testing is carried out to verify prepreg properties, such as resin content, volatile level, and flow. The resin advancement (chemical reaction) is monitored via a Differential Scanning Calorimeter (DSC) and the formulation consistency by testing the Tg via DSC or Dynamic Mechanical Analyzer (DMA). The laminate properties are also determined. All are documented and quoted on a Release Certificate. [Pg.208]

Calibration to the current spot rate yield curve, using a pre-specified volatility level and not the volatility values given by the prices of exchange-traded optiOTis. This may result in mispriced bonds and options if the selected volatilities are not accurate ... [Pg.60]

To model the complete curve, it is necessary to specify a drift rate and volatility level for/(f, T) for each T. [Pg.66]

Consider the hypothetical bond explained in Section 9.3.1. The convertible security has a price of 107.5 that includes a historical volatility of 35%. However, the convertible is valued at par (100) using the implied volatility. In practice, given all parameters and given the price of convertible bond (100), the implied volatility is a result of a goal seek value in which the percentage volatility level obtained is 25% (Figure 9.12). [Pg.186]

Volatility of the underlying stock. The higher volatility level increases the value of the option element and consequently the value of the convertible ... [Pg.200]

The option-adjusted spread (OAS) is the most important measure of risk for bonds with embedded options. It is the average spread required over the yield curve in order to take into account the embedded option element. This is, therefore, the difference between the yield of a bond with embedded option and a government benchmark bond. The spread incorporates the future views of interest rates and it can be determined with an iterative procedure in which the market price obtained by the pricing model is equal to expected cash flow payments (coupons and principal). Also a Monte Carlo simulation may be implemented in order to generate an interest rate path. Note that the option-adjusted spread is influenced by the parameters implemented into the valuation model as the yield curve, but above all by the volatility level assumed. This is referred to volatility dependent. The higher the volatility, the lower the option-adjusted spread for a callable bond and the higher for a putable bond. [Pg.221]

As exposed before, the volatility level implemented in the model is constant and assumed equal to 11%. However, in reality, the volatility tends to decrease as the bond approaches expiration. The main reason is that the probability of the issuer to call the bond back decreases in the last years of the instrument, until the... [Pg.227]

In some texts the term k is used for a. a = the constant volatility level... [Pg.77]

Equation (4.21) states that the dynamics of the forward-rate process, beginning with the initial rate/(0, J), are specified by the set of Brownian motion processes and the drift parameter. For practical applications, the evolution of the forward-rate term structure is usually derived in a binomial-type path-dependent process. Path-independent processes, however, have also been used, as has simulation modeling based on Monte Carlo techniques (see Jarrow (1996)). The HJM approach has become popular in the market, both for yield-curve modeling and for pricing derivative instruments, because it matches yield-curve maturities to different volatility levels realistically and is reasonably tractable when applied using the binomial-tree approach. [Pg.79]

Devolatilization instabilities can be caused by plugging of the vent port, variation in the vacuum level, or by variations of the volatile level in the feedstock. The efficiency of devolatilization can be improved by ... [Pg.830]


See other pages where Volatility level is mentioned: [Pg.711]    [Pg.635]    [Pg.60]    [Pg.117]    [Pg.442]    [Pg.59]    [Pg.61]    [Pg.254]    [Pg.340]    [Pg.129]    [Pg.946]    [Pg.79]    [Pg.168]    [Pg.206]    [Pg.232]    [Pg.184]    [Pg.561]    [Pg.88]    [Pg.158]    [Pg.983]    [Pg.82]    [Pg.83]   
See also in sourсe #XX -- [ Pg.187 , Pg.188 , Pg.189 , Pg.190 ]




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Volatile emissions levels over time

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