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Hydrolysis Stabilizers

Epoxides, carbodiimides, and esters of phosphorous acid can be utilized against hydrolytic degradation. [Pg.294]

Sterically hindered phenols are effective long-term and processing stabilizers for polyolefins. [Pg.294]

Phenol/phosphite combinations typically exhibit synergetic effects during polyolefin processing and are preferred. The selection of antioxidants, their total concentration, and the ratio of individual concentrations have to be adapted to each specific application [186]. [Pg.294]

At higher processing temperatures, adding a benzofuran to a phenol/phosphite system has a positive effect [186]. [Pg.294]

Typically, phenolic antioxidants are used for the long-term stabilization of polyolefins. In order to further improve long-term resistance, thiosynergists such as thioether and/or phosphites or phosphonites are added to the phenolic antioxidants as hydroperoxide decomposers. [Pg.294]


For combined cycle turbines Single lubrication system Low pour point Extreme pressure and anti-wear properties Hydrolysis stability Water separation... [Pg.284]

In the 1990s novel polyols included polyether-esters, which provided good prerequisites for flame retardancy in rigid foams and polyether carbonates with improved hydrolysis stability. [Pg.801]

Eor ionic liquids that do not mix completely with water (and which display sufficient hydrolysis stability), there is an easy test for acidic impurities. The ionic liquid is added to water and a pEf test of the aqueous phase is carried out. If the aqueous phase is acidic, the ionic liquid should be washed with water to the point where the washing water becomes neutral. Eor ionic liquids that mix completely with water we recommend a standardized, highly proton-sensitive test reaction to check for protic impurities. [Pg.26]

In the author s group, much lower-melting benzenesulfonate, tosylate, or octyl-sulfate ionic liquids have recently been obtained in combination with imidazolium ions. These systems have been successfully applied as catalyst media for the biphasic, Rh-catalyzed hydroformylation of 1-octene [14]. The catalyst activities obtained with these systems were in all cases equal to or even higher than those found with the commonly used [BMIM][PF6]. Taking into account the much lower costs of the ionic medium, the better hydrolysis stability, and the wider disposal options relating to, for example, an octylsulfate ionic liquid in comparison to [BMIM][PF6], there is no real reason to center future hydroformylation research around hexafluorophosphate ionic liquids. [Pg.240]

Rate of hydrolysis Stability Storage stability Decomposition... [Pg.9]

A new medicine that seems to be promising in this field is artimisinine (19) isolated from Artimisia annua. Extracts of this plant have been known for centuries in Chinese folk medicine under the name of Qinghaosu or Qinghao. For solubility reasons and hydrolysis stability, artimisinine is converted via the dihydro compound into water-soluble artesunate or oil soluble artemether and arteether (Scheme 5.12) [43]. [Pg.116]

Stabaxol P is used normally as a hydrolysis stabilizer in non-food polyester applications. One of the main applications is the stabilization of monofilament. An additional advantage of Stabaxol P is that it also works as a viscosity modifier. Stabaxol P has no FDA approval, and this means that it can be used only for technical applications. [Pg.524]

Both hydrolysis and condensation are reversible. Alcohols will reverse the silane hydrolysis stabilizing solution of silanols for a period of time. Solution stability measured in days or weeks can be achieved. [Pg.138]

Silane coupling agents are normally hydrolyzed to silanols before adsorption onto a surface. There are several factors which influence the hydrolysis, stability, and adsorption behavior of the silanes, including pH, type of silane used, con centration, and water content [1]. Knowledge of the stability of the silane solution is also important and may be used as a guideline in many applications. Adsorption of silane coupling agents on solid surfaces is affected by the type of surface and methods of application as well. [Pg.182]

Textiles finished with FIXAPRET PCL have very good easy-care properties, very good hydrolysis stability, and good chlorine resistance. This finish generally has no influence on the light fastness of reactive dyed or printed shades, and in the few cases where it does, the influence is only very slight. [Pg.83]

The usefulness of the product in moist crosslinking is based on its good hydrolysis stability, which permits a strongly acid catalysis e.g. with CONDENSOL FN. The chlorine resistance of finishes obtained by moist crosslinking is good, provided crosslinking is complete. [Pg.83]

FIXAPRET CPF 71 can also be used for moist and wet cross-linking. In the hydrolysis stability of the finish, It corresponds to FIXAPRET CPN. [Pg.84]

Finishes with FIXAPRET CPU have very good hydrolysis stability, but they are affected by chlorine. [Pg.84]

The hydrolysis stability of the finishes is excellent, as good as that of FIXAPRET CPN finishes. [Pg.85]

The finishes obtained with FIXAPRET PEC have good hydrolysis stability. When the product is applied by the dry curing or the moist crosslinking method, the finish has no tendency to retain chlorine. The product does not impair the shade or the light fastness of coloured goods. [Pg.85]

The third most commonly used class of flame-retardants is phosphorus-containing compounds such as phosphoric acid esters, diphenyl cre-sylphosphate, dimethyl methylphosphonate, and dibutyl dihydroxyethyl diphosphate. They have good flame-retarding performance and are effective in small amounts. They are, however, expensive and have low hydrolysis stability. [Pg.231]

Schollenberger, C. S. and Stewart, F. D., "Thermoplastic Polyurethane Hydrolysis Stability," Urethanes In Elastomers and Coatings (articles from the Journal of Elastoplastlcs) pp. 46-74, Technomlc Publ. Co., Inc., Westport (1973). [Pg.169]


See other pages where Hydrolysis Stabilizers is mentioned: [Pg.265]    [Pg.53]    [Pg.24]    [Pg.54]    [Pg.62]    [Pg.70]    [Pg.110]    [Pg.151]    [Pg.376]    [Pg.523]    [Pg.206]    [Pg.438]    [Pg.536]    [Pg.25]    [Pg.25]    [Pg.182]    [Pg.106]    [Pg.88]    [Pg.133]    [Pg.820]   


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Hydrolysis stability

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