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Bonding chemical treatment

Bonding. Surface treatment, such as chemical etch, corona, or flame treatments, is required for adhesive bonding of Tefzel. Polyester and epoxy compounds are suitable adhesives. [Pg.370]

It is possible to react an organic moiety to the hydroxyl groups on ceU waU components. This type of treatment also bulks the ceU with a permanently bonded chemical (68). Many compounds modify wood chemically. The best results are obtained by the hydroxyl groups of wood reacting under neutral or mildly alkaline conditions below 120°C. The chemical system used should be simple and must be capable of swelling the wood stmcture to facUitate penetration. The complete molecule must react quickly with wood components to yield stable chemical bonds while the treated wood retains the desirable properties of untreated wood. Anhydrides, epoxides, and isocyanates have ASE values of 60—75% at chemical weight gains of 20—30%. [Pg.330]

A factory building (Fig. 11.43) consists of two spaces a hall with mechanical extract ventilation for combined abrasive and chemical treatment and subsequent bonding and a naturally ventilated assembly hall. [Pg.1090]

Although a honeycomb lattice theoretically consists of sp2 atoms, the carbon s ability to represent intermediate states of hybridization leads to another kind of defect to counterbalance the strain energy induced by high curvature. This so-called rehybridization results in a higher n-character of the C-C bonds [24]. Furthermore, local sp3 hybridization can be induced though chemical treatment, such as after thermal elimination of functional groups. [Pg.8]

The chemical behavior of heteroatom-substituted vinylcarbene complexes is similar to that of a,(3-unsaturated carbonyl compounds (Figure 2.17) [206]. It is possible to perform Michael additions [217,230], 1,4-addition of cuprates [151], additions of nucleophilic radicals [231], 1,3-dipolar cycloadditions [232,233], inter-[234-241] or intramolecular [220,242] Diels-Alder reactions, as well as Simmons-Smith- [243], sulfur ylide- [244] or diazomethane-mediated [151] cyclopropanati-ons of the vinylcarbene C-C double bond. The treatment of arylcarbene complexes with organolithium reagents ean lead via conjugate addition to substituted 1,4-cyclohexadien-6-ylidene complexes [245]. [Pg.36]

Cooperation between the many hydrogen bonds and base-stacking interactions makes DNA very stable to chemical treatments. [Pg.152]

The cuprammonia process, the viscose process, and the acetate process have been employed for the production of rayon. Cuprammonia and viscose rayons have similar chemical and physical properties. Both are easily dyed and lose their strength when wet because of a disruption of hydrogen bonding this wet strength is improved through chemical treatment of the rayon fabrics. Acetate rayon is readily softened in the ironing process and loses its luster in boiling water. [Pg.180]

Aromatic amines are not the only type of molecule to undergo a spontaneous twist in the excited state, but DMABN is the best-studied example. Other such compounds are stilbene-type molecules, where the double bond twists in the excited state. The electronic structure for both cases, twisting double bonds and twisting single or partly double bonds of 7r-donor linked to 7r-acceptor (TICT molecules), can be related to each other and characterized in the framework of quantum-chemical treatment as described in Section III. [Pg.12]

Surface modification of LDPE film can also be brought about by chemical treatment [118] with an aqueous solution of ammoniacal ammonium persulphate in the presence of Ni+2 ions under variable reaction conditions. The investigation of treated surface showed the presence of polar groups (viz. carbonyl and hydroxyl) in the infrared (IR) spectroscopy, with characteristic bands at 1700, 1622 and 3450 cm-1. It is known that the persulphate ion attacks the double-bond-producing epoxy or diol group. However, the destructive oxidation of saturated hydrocarbons does not occur with persulphate alone, but requires the presence of the nickel (II) ion. The authors have proposed the following mechanism of chemical treatment ... [Pg.252]

Recently, 2-hydroxypropyl cellulose (HPC) was demonstrated to be a very suitable matrix for UV/Vis absorption study of photoyellowing of milled-wood lignin in the solid state [10] where clean kinetics of discolouration were established after different chemical treatments of the lignin in solution. This indicates the importance in the discolouration process of phenolic structures without carbonyl groups and conjugated double bonds. The present communication describes a similar photochemical study on quinones and hydroquinones incorporated in HPC films under comparative concentrations ( 6.5xl0"5 mol/g HPC). For comparison, we also use UV/Vis reflectance spectroscopy to examine the behaviour of these compounds adsorbed on filter paper after light-exposure. [Pg.61]


See other pages where Bonding chemical treatment is mentioned: [Pg.258]    [Pg.152]    [Pg.260]    [Pg.442]    [Pg.2149]    [Pg.2359]    [Pg.985]    [Pg.145]    [Pg.381]    [Pg.370]    [Pg.181]    [Pg.308]    [Pg.596]    [Pg.234]    [Pg.85]    [Pg.419]    [Pg.61]    [Pg.215]    [Pg.310]    [Pg.199]    [Pg.65]    [Pg.644]    [Pg.218]    [Pg.167]    [Pg.442]    [Pg.258]    [Pg.121]    [Pg.203]    [Pg.108]    [Pg.142]    [Pg.56]    [Pg.228]    [Pg.121]    [Pg.220]    [Pg.96]    [Pg.370]    [Pg.450]   
See also in sourсe #XX -- [ Pg.95 ]




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