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Anticorrosion layers

Various copolymers with the basic backbone of —Ar—NH—Ar—S—, i.e., aromatic amino sulfide copolymers have been synthesized. This type of copolymer is semiconducting and can be used in many electronic and electro-optical applications. Examples of such applications are antistatic layers, electromagnetic-shielding layers, anticorrosion layers, batteries, electroluminescent devices, and in electronic circuits, such as conductor tracks of transistors. [Pg.196]

Fig. 1. Release force of Pseudo Bamcles (Epoxy studs ) from reference surfaces versus measured surface energy. The epoxy coatings is a marine anticorrosion layer the phenyl silicone systems are typical of hard cookware coatings PDMS 1,2,3.4 are soft PDMS-based systems with different filler types and levels, typical of fouling release coatings the fluorosilicone is a trifluorpopylmethyl-dimethyl silicone elastomeric coating... Fig. 1. Release force of Pseudo Bamcles (Epoxy studs ) from reference surfaces versus measured surface energy. The epoxy coatings is a marine anticorrosion layer the phenyl silicone systems are typical of hard cookware coatings PDMS 1,2,3.4 are soft PDMS-based systems with different filler types and levels, typical of fouling release coatings the fluorosilicone is a trifluorpopylmethyl-dimethyl silicone elastomeric coating...
Tungsten-copper-boron nitride pseudoalloy electrodes have been tested in electric discharge machining of hard alloys [101,102]. Alloys used in the manufacture of electric contacts are frequently composites of metals and a-BN, providing for increased heat durability [103]. Thus, silver cermet electrical contact material for circuit breakers is made by hot-pressing of the constituents [104 to 106]. Again, Ag/BN composite layers can also be prepared by electrodeposition [107]. Zinc alloys as used in coating sheet steel as anticorrosion layers may contain dipersed a-BN for increased weldability and corrosion resistance [108 to 111]. [Pg.102]

Scratching was performed on galvanised steel samples coated with anticorrosion layers such as ppHMDSO or chromated layers. This simulates severe damage caused to these layers. [Pg.223]

For formation of anticorrosive and adhesion-improving protective layers on metals the cleaned surface is treated with aqueous acidic solution containing molybdate, chromium fluoride, phosphate, acetate, and Zn ions. As dispersant a mixture of 60% alkali salt of a phosphate ester, 20% alkylpolyglucoside, and 20% fatty alcohol ethoxylate was applied. This method passivates the metal surface by formation of an anticorrosive and protective layer that improves adhesion of subsequent coatings. [Pg.604]

The preparation of a corrosion inhibitor in the solid form allows the development of a new technique of continuous intensive anticorrosive protection for gas and oil pipelines, as well as for acidizing operations of oil wells [746]. The controlled dissolution of the solid inhibitor creates a thin protective layer on the metallic surface that prevents or minimizes the undesirable corrosion reactions. [Pg.85]

Benzotriazole has also been used as an additive in anticorrosive coatings for silver layered on plastic film <89JAP8909733). An anticorrosive, electromagnetic wave-shielding coating containing tolyltriazole has been developed for aluminum <91EUP437979). [Pg.124]

Surface Preparation of the Substrate. This is extremely important for all methods of paint and coatings application. The failure of a paint system is often due not to the paint itself, but because of a failure in surface preparation. For example, an anticorrosive paint applied to a rusty surface will not be effective if the rust falls off taking the new paint with it. For wood and plastic surfaces, old paint or a weathered surface layer may have to be removed. For older metal objects, the removal of corrosion is often required. Sandblasting is one method to remove both the old paint and any corrosion. For new metal objects, a phosphate or chromate layer is often chemically bonded to the metal to provide a surface to which a coating can easily adhere. [Pg.1199]

Before applying nonfouling paints, the cleaned surface of the hull is covered with an adhesive sublayer or a layer of adhesion promoter, and anticorrosion paint. In seawater tests panels covered with these paints do not foul even after 27 months of exposition panels covered with normal paints fouled by 100% already after 2 months. The serviceability of paints... [Pg.488]

The inhibitive properties of molybdate-based anticorrosive pigments are attributed to the ability of molybdate ions to pass into solution, and to migrate to the metal surface resulting in the formation of a protective layer on the substrate, which insulates (passivates) the metal from attack and prevents corrosion [5.91]. [Pg.220]

Another interesting and widely studied case is the formation of porous metal oxides by anodization of metals. Here, the electrolytic procedure yields a thin layer of porous materials applicable in catalysis, in anticorrosion, batteries, and other applications. Such materials will be discussed in Chapter 6. [Pg.8]

The deposits of zinc on different metals, especially on steel, have special relevance because of their anticorrosive properties by the formation of passive layers on contact with air, and in aqueous medium. [Pg.753]

Laminates (multilayer structures), where each layer itself may be either a single-phase material or a multiphase material [10]. Examples of laminates include some electronic components, many structural composites, adhesive joints, and any other fabricated article where a coating layer (such as an anticorrosion coating or paint) is deposited on another material. See sections 7.C and ll.C.S.d for earlier discussions of such structures in this book. [Pg.689]

We also see that cupric ions react as a catalyst on rust coagulation and prevent rust crystallization into coarse aggregates [95,96], The rust then remains amorphous and develops a dense, void-free barrier layer of anticorrosive rust. Transition metal ions such as Tif+ Or Cr t, and Nr+ which come from alloying elements in weathering steels, are also found to catalyze the formation of amorphous or poorly crystalline iron rust [97,98]. It is commonly known that the amorphous rust of FeOOH is much more anticorrosive than the coarse crystalline deposits of iron rust. [Pg.585]

Matthews, 2000). A phosphate salt solution and an aqueous suspension of HAp powder were used as an electrolyte for PEO and EPD, respectively. The corrosion resistance was assessed by potentiodynamic polarisation tests in a buffered physiological solution (see also Kwok et al., 2009). The results of this study indicated that a hybrid combination of PEO and EPD produces an osseoconductive phase-pure ITAp layer and an anticorrosive titania interlayer that promise to provide good mechanical and biochemical stability in the highly corrosive environment of the human body. Other studies involving titania bond coats include Albayrak and Altintas, 2010 Paluszkiewicz, Dlugon andKwiatek, 2012 Rath etal., 2012 and Jain etal. (2013). [Pg.156]

This section does not cover the topic of coatings and finishes. These finishes are usually highly formulated and are applied as multiple-pass coatings which include special primers and intermediate layers. They may include pigments, additives, other resins, and more than one fluoropolymer. The main applications of fluoropolymer finishes are in cookware and industrial anticorrosion and high-temperature uses. A separate volume, Fluorinated Coatings and Finishes, a Plastics Design Library (PDL) volume in the Fluorine Handbook Series published by William Andrew, Inc., covers the topic. [Pg.185]

Surface modification is broadly used in controlling the surface properties of fillers in rubber, synthetic polymers and other materials (see Chapter IX). The surfactant adsorption layers that make surfaces hydrophobic are used to prevent caking in hygroscopic powders (fertilizers), as anticorrosive agents and in numerous other processes. [Pg.248]


See other pages where Anticorrosion layers is mentioned: [Pg.443]    [Pg.443]    [Pg.443]    [Pg.538]    [Pg.552]    [Pg.9404]    [Pg.265]    [Pg.494]    [Pg.443]    [Pg.443]    [Pg.443]    [Pg.538]    [Pg.552]    [Pg.9404]    [Pg.265]    [Pg.494]    [Pg.366]    [Pg.202]    [Pg.223]    [Pg.225]    [Pg.734]    [Pg.28]    [Pg.194]    [Pg.641]    [Pg.645]    [Pg.651]    [Pg.63]    [Pg.271]    [Pg.452]    [Pg.278]    [Pg.223]    [Pg.42]    [Pg.583]    [Pg.584]    [Pg.585]   
See also in sourсe #XX -- [ Pg.196 ]

See also in sourсe #XX -- [ Pg.142 ]




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