Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Additive loss

Two amides were used in applications with ethylene vinyl acetate coply-mer. ° The chemical composition of these amides is not disclosed. If films were kept at 40°C for about 30 minutes, the surface concentration of one amide was increasing with time whereas the concentration of the second amide was rapidly decreasing. The second amide was not available on surface of film at 50°C whereas the first amide disappeared from surface only at 65°C. There is no additional data which explains the reasons but they must be related to different thermal stability of the two compounds. [Pg.74]

Increase of aging temperature from room to 55°C rapidly depleted surface emcamide in POP/LLDPE film.  [Pg.74]

These few data show that it is important to learn more about retention of additives under discussion, especially that in some cases problems were arising from using material at elevated temperature which caused decrease in coefficient of friction which affected transportation of pellets. It is also important for future research to study effect of surface washing because in some instances additive manufacturers suggest removal of surface additives by washing to prevent adhesive failures. [Pg.75]

1 Quijada-Garrido, L de Velasco-Ruiz, M. R Barrales-Rienda, J. M. Macromol. Cheni. Phys., 201, 3,375-81,2000. [Pg.75]

9 Botros, M. G, Annual Technical Conference - Society of Plastics Engineers, 3653-59,1995. [Pg.75]


When the relative pressure falls to P2/p°, corresponding to r = 80 A, the second group of pores will have given up a volume of adsorbate equal to dv 22-But since the film thickness has now diminished to t2, there will have been an additional loss from the walls of group 1 the total loss from group 1 is therefore so that the total loss from both groups is... [Pg.144]

Dynamic mechanical measurements were made on PTEE samples saturated with various halocarbons (88). The peaks in loss modulus associated with the amorphous relaxation near —90°C and the crystalline relaxation near room temperature were not affected by these additives. An additional loss peak appeared near —30° C, and the modulus was reduced at all higher temperatures. The amorphous relaxation that appears as a peak in the loss compliance at 134°C is shifted to 45—70°C in the swollen samples. [Pg.352]

The power P is only that imparted to the liquid by tbe impeller. It is not tbat delivered to tbe motor drive, which additionally includes losses in the motor and speed-reducing gear. These may total 30 to 40 percent of P A stuffing box where tbe shaft enters a covered vessel causes additional losses. [Pg.1469]

Loss computation, this enables the operator to ensure that the filters are clean and that no additional losses than necessary reduce the performance of the gas turbine. The following parameters are necessary to monitor the filter ... [Pg.703]

Temperature of the system When inhibitors are used in the 0-100°C range it is usually found that higher concentrations become necessary at the higher temperatures Other inhibitors can lose their effectiveness altogether as the temperature is raised. A prime example of this is the polyphosphate type of inhibitor. This is effective in circulating systems at temperatures below about 40°C, but at higher temperatures reversion to orthophosphate can occur and this species is ineffective at the concentrations at which it will then be present. If calcium ions are present, additional loss of inhibitor will occur due to calcium phosphate precipitation. [Pg.783]

The cyclopentene derivatives 9 undergo both 1,5- and 1,7-dipolar electrocyclizations to yield mixtures of pyrazoles 10 and benzodiazepines 11. In addition, loss of nitrogen results in the carbenes 12, which cyclize to the tetrahydrocyclopent[fl]indenes 13.117... [Pg.352]

This results from the slow kinetics of methanol oxidation and oxygen reduction. An additional loss is due to the cell resistance (arising mainly... [Pg.71]

The analysis of an unknown number of unknown additives in unknown concentration in an unknown polymeric matrix is a demanding task for the analytical chemist for a variety of circumstances (Table 2.1). Primary analytical needs include the identification of the additives, the quantification of the additive levels, and the examination of additive stability. Obviously, the experimental analytical conditions must be such that no measurable polymer degradation or additive loss occurs during analysis. [Pg.29]

Apart from recapture of the injected electrons by the oxidized dye, there are additional loss channels in dye-sensitized solar cells, which involve reduction of triiodide ions in the electrolyte, resulting in dark currents. The Ti02 layer is an interconnected network of nanoparticles with a porous structure. The functionalized dyes penetrate through the porous network and adsorb over Ti02 the surface. However, if the pore size is too small for the dye to penetrate, that part of the surface may still be exposed to the redox mediator whose size is smaller than the dye. Under these circumstances, the redox mediator can collect the injected electron from the Ti02 conduction band, resulting in a dark current (Equation (6)), which can be measured from intensity-modulated experiments and the dark current of the photovoltaic cell. Such dark currents reduce the maximum cell voltage obtainable, and thereby the total efficiency. [Pg.747]

Ketene acetals show a pattern of product formation very similiar to enamines79 Diphenyl-4,4-diacetyl triafulvene is converted to diacetylmethyl cyclopentadiene 529 by S,N-acetals, whilst diphenyl-4,4-dicyano triafulvene undergoes C—C-inser-tion to S,N- and N,N-acetals, e.g. 530/531, resulting in cross-conjugated systems 533/534 by analogy with enamines. Cyclic S,N-acetals 532, however, yield exclusively the bicyclic fulvenes 535 due to additional loss of methyl mercaptan. [Pg.106]

The pre-exponential factor Ac H for the reaction R02 + RH per attacked C—H bond differs for aliphatic hydrocarbons and for hydrocarbons, where the attacked C—H bond is in the a-position to tt-C—C bond. This difference is the result of additional loss of the activation entropy due to retardation of group rotation, resulting from the interaction of tt-electrons with electrons of reaction center. When the peroxyl radical attacks the C—H bond in neighborhood with the n-C—C bond, the retardation of free rotation around the C—C bond in the transition state additionally lowers the entropy of the transition state. The values of E0 and AC H are given here [119] ... [Pg.74]

Adults require 1-2 mg of copper per day, and eliminate excess copper in bile and feces. Most plasma copper is present in ceruloplasmin. In Wilson s disease, the diminished availability of ceruloplasmin interferes with the function of enzymes that rely on ceruloplasmin as a copper donor (e.g. cytochrome oxidase, tyrosinase and superoxide dismutase). In addition, loss of copper-binding capacity in the serum leads to copper deposition in liver, brain and other organs, resulting in tissue damage. The mechanisms of toxicity are not fully understood, but may involve the formation of hydroxyl radicals via the Fenton reaction, which, in turn initiates a cascade of cellular cytotoxic events, including mitochondrial dysfunction, lipid peroxidation, disruption of calcium ion homeostasis, and cell death. [Pg.774]

Chemical and hydrocarbon plant losses resulting from fires and explosions are substantial, with yearly property losses in the United States estimated at almost 300 million (1997 dollars).1 Additional losses in life and business interruptions are also substantial. To prevent accidents resulting from fires and explosions, engineers must be familiar with... [Pg.225]

Although there is an additional loss of charge with the overflowing liquid, the system is still operating under hazardous conditions, c. After the inlet flow is stopped, (7s)in and (/s)out are zero, and Equation 7-36 reduces to... [Pg.330]

As a final note, there was a tenth chapter intended for this volume to be written by Andre Collet. He had agreed to write this chapter but could not, adding one additional loss among many of far greater importance arising from the death of this eminent stereochemist and gentleman and friend to so many. [Pg.618]

Mumenthaler [1.82] discovered similar problems, as already mentioned freezing in a fluidized bed with C02 clogs the filters, reducing the yield to only 80-90 %, with an additional loss of 10 % fines. [Pg.109]

MRE has not been validated on hard materials, i.e., for shear moduli greater than 200 kPa. The reasons for this are obvious. In rigid matter, shortened T2s will prevent accurate measurements, particularly when using MRI. Moreover, low flexibility induces small strain and an additional loss... [Pg.238]

Alvarez-Toledano has investigated149 the reactivity of tertiary amines toward vinylketene complexes of type 221 and found that a number of unusual transformations take place. The formation of 237 and 238 is not directly linked to the presence of the amine, but instead relies on a thermo-lytic coupling of two carbene complexes formed from the vinylketene ligand, with additional loss of carbon monoxide. It is thought that 239 is formed by the deprotonation of the labile C-4 proton, followed by subsequent coordination of a capping Fe(CO)3 group. [Pg.340]

However, a series of factors introduce losses in the system namely, the reflectivities of the mirrors (RiandR2) on the figure, which reflect only a fraction, Ri and R2, of the intensity. Additional losses can be produced by absorption in the windows of the cell that contains the active medium (if this is the case), diffraction by apertures, and scattering due to particles or imperfect surfaces. All of those losses can be included in a loss factor per trip, expressed as e. Thus, considering both amplification and intensity decrease per round trip, the intensity after a single round trip through a resonator of length d is... [Pg.49]

Somfai enhanced the driving force of some amide enolate aza-Claisen rearrangements by choosing vinylaziridines as reactants [24]. The additional loss of ring strain offered the advantage of running most of the reactions at room temperature to synthesize unsaturated chiral azepinones. Various substitution... [Pg.170]

One may argue that the loss could be smaller if T were made shorter however, secondary reactions necessary to stabilize the reaction products must be exergonic which will thus incur additional losses. [Pg.211]


See other pages where Additive loss is mentioned: [Pg.1170]    [Pg.2861]    [Pg.312]    [Pg.651]    [Pg.2232]    [Pg.368]    [Pg.62]    [Pg.281]    [Pg.311]    [Pg.188]    [Pg.455]    [Pg.243]    [Pg.47]    [Pg.406]    [Pg.178]    [Pg.62]    [Pg.112]    [Pg.51]    [Pg.318]    [Pg.285]    [Pg.59]    [Pg.48]    [Pg.113]    [Pg.306]    [Pg.134]    [Pg.25]    [Pg.17]    [Pg.124]    [Pg.243]    [Pg.37]   


SEARCH



© 2019 chempedia.info