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Stabilizing additive

Oxidation. AH polyamides are susceptible to oxidation. This involves the initial formation of a free radical on the carbon alpha to the NH group, which reacts to form a peroxy radical with subsequent chain reactions leading to chain scission and yellowing. As soon as molten nylon is exposed to air it starts to discolor and continues to oxidize until it is cooled to below 60°C. It is important, therefore, to minimize the exposure of hot nylon to air to avoid discoloration or loss of molecular weight. Similarly, nylon parts exposed to high temperature in air lose their properties with time as a result of oxidation. This process can be minimized by using material containing stabilizer additives. [Pg.270]

PL can be used as a sensitive probe of oxidative photodegradation in polymers. After exposure to UV irradiation, materials such as polystyrene, polyethylene, polypropylene, and PTFE exhibit PL emission characteristic of oxidation products in these hosts. The effectiveness of stabilizer additives can be monitored by their effect on PL efficiency. [Pg.379]

Outdoors Well-spaced tanks, possibly with water cooling, refrigeration, buried Some monomers (e.g. acrylic acid) may require provisions to avoid freezing Provision for inhibitor/stabilizer addition Provision for atmosphere inerting may be required ... [Pg.249]

Usually, prolonged boiling in acid water and then in alkaline water is used to stabilize NS. However, there are claims that boiling with alkaline water decreases NS stability (Ref 28). However, in a previous publication (Ref 27) these same authors claim that kler-boiling or pro-longed boiling in water or in dilute alkaline soln improves stability. Addition of substances such as epichlorohydrin that swell the NS and aid water penetration is claimed to improve stability (Ref 16)... [Pg.343]

Polymers can be radiation protected by stabilizing additives (antirads) through two principal... [Pg.860]

Studies have shown that carbene reactivity toward a wide variety of substrates is dramatically affected by the nature and multiplicity of the electronic state. - Similarly, the structure, electronic state, thermochemical stability, and reaction kinetics of both singlet and triplet carbenes can be significantly affected by the R-substituents. If R provides steric hindrance, the carbene center can be shielded to slow down inter-molecular reactions (kinetic stabilization). Additionally, bulky and/or geometrically... [Pg.289]

Stabilizing additives for polymers usually scavenge free radicals or hydroperoxides from the system. The effect of such additives is depicted in reactions... [Pg.458]

Foams for woodland and grass fire-fighting have been developed with low drainage (water loss from foam) and high expansion (volume of foam per volume of starting liquid), two parameters traditionally considered to be inversely proportional. The stabilizing additive is poly (methyl vinyl ether/maleic anhydride), thought to cross-react with fatty alcohol components of the foam base via the anhydride function. [Pg.450]

When a molecule accepts electrons, the electrons tend to go to places where/1 (r) is large because it is at these locations that the molecule is most able to stabilize additional electrons. Therefore a molecule is susceptible to nucleophilic attack at sites where/ "(r) is large. Similarly, a molecule is susceptible to electrophilic attack at sites where f (r) is large, because these are the regions where electron removal destabilizes the molecule the least. In chemical density functional theory (DFT), the Fukui functions are the key regioselectivity indicators for electron-transfer controlled reactions. [Pg.256]

It has already been mentioned how high Tm s correlate with a lower susceptibility to aggregation and the preferred solution conditions in which M-CSF, IL-1R (types I and II), Flt3L, and CD40L are stabilized. Additionally, G-CSF... [Pg.342]

There is an alternative mechanism, radiative emission, that can lead to stabilized addition products at low pressures (see Chapters 2 and 3). The excited intermediate can radiate an IR photon to lose sufficient excess energy (though not necessarily all the excess energy) to stabilize itself with respect to dissociation. This process typically has a rate of5-1000 s , so normally is not competitive with dissociation, but there are cases known where certain structural features enhance radiative emission and it can become an important competitor to other chemistry. For methoxide addition to acrylonitrile, nevertheless, it is imlikely to be an operating mechanism. ... [Pg.206]

Alkene polymers such as poly(methyl methacrylate) and polyacrylonitrile are easily formed via anionic polymerization because the intermediate anions are resonance stabilized by the additional functional group, the ester or the nitrile. The process is initiated by a suitable anionic species, a nucleophile that can add to the monomer through conjugate addition in Michael fashion. The intermediate resonance-stabilized addition anion can then act as a nucleophile in further conjugate addition processes, eventually giving a polymer. The process will terminate by proton abstraction, probably from solvent. [Pg.400]

All the reactions described so far are carried out using stoichiometric amounts of Co2(CO)8. However, a coordinatively unsaturated 02(00)5 species would be liberated when the rearrangement proceeds, and if this cobalt species could form an alkyne-Co2(CO)6 complex with another molecule of 1-(1-alkynyl) cyclopropanol, the reaction should proceed with only a catalytic amount of 02(00)8 [13, 18]. In practice, when 1-phenylethynylcyclopropanol (11b) is treated with a 10 or 20 mol% amount of 02(00)8, the rearranged product 13b is obtained in 43 and 59 % yield, respectively. Thus, the reaction in fact proceeds with a catalytic amount of 02(00)8 however, the efficiency is low and a complex mixture of by-products is also obtained. As this low efficiency could be ascribed to instability of the unsaturated cobalt species, the catalytic reaction could be made more efficient by the addition of a stabilizing additive. [Pg.77]

UV stabilizer Additive that retards degradation caused by UV radiation, vulcanization Cross-linking with heat and sulfur. [Pg.495]

The ARCHON in situ mixer unit consists of a hydraulically powered grinding/mixing head, typically attached to a long-reach backhoe or to a wide-track bulldozer for extensive wet areas. The process is designed to feed a continuous supply of chemical fixation and stabilization additives, which are added to the waste during the grinding/mixing operation. [Pg.1074]

Kumar, K. and Mishra, H. N. (2004). Mango soy fortified set yoghurt Effect of stabilizer addition on physicochemical, sensory and textural properties. Food Chem. 87, 501-507. [Pg.242]

A fuel oil stabilizer additive listed in QPL-24682 may be blended into naval distillate fuel at rates up to 35 lb/1,000 barrels to protect against degradation and improve storage stability as measured by ASTM D-5304. Method ASTM D-2274 may also be used if the test duration is extended from 16 to 40 hours. [Pg.142]

It should be noted that many types of stabilizers are employed, and each polymer system is unique and requires its own particular heat-stabilizer additives. [Pg.131]

Transmetallation of the dimetallic species 186a or 186b with CuCN led to a new organometallic species formulated as 191 which displayed remarkable thermal stability. Addition of reactive alkylating agents such as allyl bromide to 191 directly produced compound 192. Indeed, once the first alkylation occurred, the copper salts present in... [Pg.910]


See other pages where Stabilizing additive is mentioned: [Pg.203]    [Pg.47]    [Pg.118]    [Pg.204]    [Pg.91]    [Pg.251]    [Pg.2]    [Pg.462]    [Pg.126]    [Pg.260]    [Pg.264]    [Pg.453]    [Pg.119]    [Pg.158]    [Pg.276]    [Pg.8]    [Pg.95]    [Pg.324]    [Pg.356]    [Pg.469]    [Pg.494]    [Pg.441]    [Pg.293]    [Pg.370]    [Pg.239]    [Pg.158]    [Pg.252]    [Pg.117]    [Pg.265]   
See also in sourсe #XX -- [ Pg.18 ]

See also in sourсe #XX -- [ Pg.376 ]




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1,3-Butadiene, 1,2-addition reactions stability

Addition of Stabilizers

Addition, stabilized carbanions

Additional Factors That Govern Complex Stability

Additional Stability Checks

Additional Stabilizing Influences

Additives Dimensional stability

Additives UV stabilizers

Additives heat stabilizers

Additives light stabilizers

Additives ultra-violet stabilizers

Additives, enzyme stabilization

B Addition to Generate Metal-Stabilized Cations

Based on Deprotonation of Selenides that have an Additional Anion-stabilizing Group

Conjugate Addition of Stabilized Carbanions asahiko Yamaguchi

Conjugate Addition of Stabilized Carbon Nucleophiles

Conjugate addition anion-stabilizing substituents

Conjugated diene, 1,2-addition stability

Contents 2 1,4-Addition of R (aryl or vinyl) and stabilized carbanions

Delocalization Energy Is the Additional Stability Delocalized Electrons Give to a Compound

Dimensional Stability Additives for TDI

Dispersing powders stabilizer addition

Enantioselective Conjugate Additions of Enolates and other Stabilized Carbon Nucleophiles

Enolate anions, addition reactions resonance stabilization

Enolate anions, addition reactions stabilities

Enone. conjugate addition reaction with stability

Foam-Stabilizing Organic Additives

Heat stabilizers, additive coloring effects

Heat stabilizers, additive composite

Heat stabilizers, additive fatty acid

Heat stabilizers, additive organic compound

Heat-stabilizing additives

Hindered amine light stabilizer additives

Immobilization stabilizing additives

Light stabilizer, additive categories

Light stabilizer, additive mechanisms

Michael Additions of Stabilized Anions

Nitrile stabilized anions addition reactions

Nitrogen stabilization carbonyl compound addition reactions

Oxidative addition adduct stability

Plastics additives thermal stabilizers

Polymer stabilization interactions with other additives

Prediction of Electrolyte and Additive Electrochemical Stabilities

Protein addition, enzyme stabilization

Stabilisation stabilizing additives

Stability nucleophilic addition

Stabilizers additives

Stabilizers additives

Sugar additives, enzyme stabilization

Thermal stability/stabilization halogenated additives

Typical Additives and Solution Stabilizers

Ultraviolet stability additive coloring effects

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