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Aluminum lead—oxygen bonds

Introduction into polymethyl methacrylate of disperse zinc or aluminum at the point of polymerization leads to a marked stabilization of the polymer filled only with zinc (Figure 6.4, curves 4-6), on which effect related to the nonchain inhibition of the thermal-oxidative degradation due to breaking of the oxygen bond by unoxidized particles of zinc. Since aluminum particles are covered with thick layers of oxide film, they exert practically no stabilizing influence on the thermal-oxidative degradation of the polymer (Figure 6.4, curves 1 and 2). [Pg.160]

Agreement with the electrostatic valence rule is satisfactory except for the oxygen atoms G (Fig. 4), common to only three oc-tahedra. It is seen, however, that these atoms occur in groups of four, which can be combined to tetra-hedra by placing aluminum ions in positions 4e, the total bond strengths then becoming 2 . The four chlorine ions occupy positions 4 c, 4 b being ruled out by the small Cl -0= distance it leads to (2.72 A, sum of radii 3.21 A). [Pg.548]

The addition of thiols to C—C multiple bonds may proceed via an electrophilic pathway involving ionic processes or a free radical chain pathway. The main emphasis in the literature has been on the free radical pathway, and little work exists on electrophilic processes.534-537 The normal mode of addition of the relatively weakly acidic thiols is by the electrophilic pathway in accordance with Markovnikov s rule (equation 299). However, it is established that even the smallest traces of peroxide impurities, oxygen or the presence of light will initiate the free radical mode of addition leading to anti-Markovnikov products. Fortunately, the electrophilic addition of thiols is catalyzed by protic acids, such as sulfuric acid538 and p-toluenesulfonic acid,539 and Lewis acids, such as aluminum chloride,540 boron trifluoride,536 titanium tetrachloride,540 tin(IV) chloride,536 540 zinc chloride536 and sulfur dioxide.541... [Pg.316]

Many metals, such as zinc, iron, lead, copper, and aluminum are found chemically bonded to oxygen in nature. Sometimes, chemists can use single displacement reactions to get the pure metal. [Pg.38]

These catalysts are the alkoxyderivatives of aluminum, titanium, lead, tin. This study shows that the interaction of oligoalkylhydridesiloxane with tetrabutoxytitanium first forms coordination bonds due to the donor-acceptor interaction of the titanium atom with the oxygen atoms in oligosi-loxane. This is followed by the polymerisation of oligosiloxane, which forms a spatially cross-linked polymer. [Pg.235]

We consider this to be proof, that the ionic liquids supported on a metal oxide form a covalent bond between the aluminum of the chloroaluminate species and the oxygen of the hydroxyl-groups on the surface of the carrier (Figure 13). This is important for the stability of the immobilised ionic liquids since a leaching of the ionic liquid is prevented. As shown in the case of immobilised ILs based on iron chloride, the lack of strong bond between anion and surface leads to leaching. [Pg.89]

Alpha-lead azide crystals, wrapped in a thin aluminum foil, were subjected to fast and thermal neutrons in a heavy-water reactor [53]. With a thermal flux rate of about 10 n/cm /sec, the crystals were irradiated for 8, 17, and 170 hr. The crystals decomposed to a brown powder, which was identified as lead carbonate by X-ray diffraction and infrared absorption. From a mass spectrographic analysis of the isotopes of carbon and oxygen in the decomposition products, it was determined that the carbonate was formed fiom the atmosphere by the breaking of surface bonds by the neutrons. It was subsequently reported [54] that the total dose required for conversion to lead carbonate is approximately 7.5 X 10 n/cm ... [Pg.217]


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Aluminum-oxygen

Lead—oxygen bonds

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