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Surface unbonds

Surface unbonds are an alternative form of void, often caused when adhesive is applied to one adherend only and unevenly. Zero-volume unbonds occur where the adhesive and adherend are in contact, but there is no significant bond strength between them. Such defects may be caused by poor surface preparation, failure to remove completely the manufacturer s backing film, a loose substrate, and so on. [Pg.80]

In joining reinforced thermosetting pipe it is particularly important that the pipe be cut without chipping or cracking it. It is also important to sand, file, or grind any mold-release agent from the surfaces to be cemented. Joints are built up layer by layer of adhesive-saturated reinforcement by following the manufacturer s recommended procedure. Application of adhesive to the surfaces to be joined and assembly of these surfaces shall produce a continuous bond and provide an adhesive seal to protect the reinforcement from attack by the contents of the pipe. Unfilled or unbonded areas of the joint are considered defects and must be repaired. [Pg.1005]

It is clear from examination of the fracture surface and weld cross sections that the weld was improperly formed, resulting in an irregular plane of unbonded metal. The smoothly rippled, spherical contours in some regions of the fractured area are evidence of solidification of the weld metal along a free surface that was not in contact with the plate. Substantial porosity is apparent. [Pg.350]

The first type of bonded design for this application was the beaded doubler panel (Fig. 28). This design was fairly successful at addressing the problems with simple riveted structure but had two primary drawbacks. The area under the beads remained a single thickness sheet and was still prone to fatigue. Reducing the unbonded areas under the beads was not a solution because it reduced the overall stiffness of the panel. Secondly, tooling for these panels was complex and not very robust. Autoclave pressure applied to the beaded areas of the doubler would cause them to collapse, so thick frames were fabricated with cutouts for the beads to protect them. A rubber layer bonded to the surface of the frames... [Pg.1175]

The nondestructive temperature differential test by infrared is used. In this method, heat is applied to a product and the surface is scanned to determine the amount of infrared radiation is emitted. Heat may be applied continuously from a controlled source, or the product may be heated prior to inspection. The rate at which radiant energy is diffused or transmitted to the surface reveals defects within the product. Delaminations, unbonds, and voids are detected in this manner. This test is particularly useful with RPs. [Pg.304]

Secondly, the unbonded surface Au atoms are much more numerous than the core atoms. Lack of experimental observation of a shoulder on the low b.e. side of the AU4/7/2 peak therefore argues for an assignment of the first component in the Au4/ peak to the surface Au atoms. Accordingly, as may be seen in Table 2, in the presently proposed fitting, the lowest b.e. component of the peak is assigned to the unbonded gold surface atoms. [Pg.29]

Small pressure transducers with flush-mounted diaphragms are commercially available for the measurement of either steady or fluctuating pressures up to 100 MPa (about 15,000 Ibftin ). The metallic diaphragms are as small as 4.8 mm (%6 in) in diameter. The transducer is mounted on the apparatus containing the fluid whose pressure is to be measured so that the diaphragm is flush with the inner surface of the apparatus. Deflection of the diaphragm is measured by unbonded strain gauges and recorded electrically. [Pg.9]

Fig. 10.6. Signals reflected from the top and bottom surfaces of a 40 pm thick layer of polypropylene, with the same acoustic parameters as in Fig. 10.4 (a) bonded to steel (b) unbonded, with air backing (Sinton etal. 1989). Fig. 10.6. Signals reflected from the top and bottom surfaces of a 40 pm thick layer of polypropylene, with the same acoustic parameters as in Fig. 10.4 (a) bonded to steel (b) unbonded, with air backing (Sinton etal. 1989).
A purpose designed CEC stationary phase that gives excellent EOF character yet allows rapid simultaneous acidic, basic and neutral separations under isocratic conditions without tailing is yet to be discovered. Nevertheless, the Hypersil BDS unbonded silica used in this work was taken forward to explore such complex mixture separations as it combines features of both pure and traditional media. As a phase, it possesses a reasonable EOF (as it is based on traditional silica) with a lower number of activated silanol groups on the silica surface (due to the pre-treatment procedure used to remove surface metal contamination). Figure 3.3 shows the separation of benzylamine, caffeine and p-hydroxybenzoic acid in a single chromatographic analysis. [Pg.106]

Plasma. A plasma is used to clean the electrode surface, leaving unbonded surface atoms and, thus, an activated surface. Carbon is much used for this subsequent exposure to amines or ethenes, for example, results in chemical bond formation. Plasma discharge in the presence of radical monomers in solution, leading to polymer formation on the surface, is equivalent to chemical activation. The use of lasers in this area may be interesting, but has been little exploited as yet. [Pg.317]

To understand the role of the surface silanols and their contribution to retention, these compounds were separated on a column that was purposely coated to half of the Cjg level of the original Clg (Fig. 5-21b) (coated column had approximately 50% silanol content). If peak tailing is due solely to the silanol interaction, the peak symmetry should be worse than on the fully coated column. But there was no decrease in peak symmetry. In fact, retention of the tetracaine (peak 4) increased slightly while the peak symmetry improved. Thus, it appears that silanols do contribute to retention but the amount of silanols is not the main cause of peak asymmetry. The logical extension of this approach is to separate the compounds on unbonded silica gel, as shown in Figure 5-27c. In this situation, peak symmetry is quite good and retention is decreased. [Pg.165]

Let us return to a further description of the electronic structure at the surface of the crystal. Imagine constructing the electron states in a crystal with a surface, just as bulk states were constructed in Chapter. 1. Bond orbitals are formed for all the bond.s, but those hybrid orbitals directed out of the surface remain unbonded. These orbitals are allied dangling hybrids. Each retains the energy C, seen in Fig. 3-.3 to be greater than the bond energy by V. (We are interested in total... [Pg.232]

It is not possible to bond all the surface silanol groups of a silica packing. Untreated silanols are capable of adsorbing polar molecules, which will affect the chromatographic properties of the bonded phase. Usually, these untreated silanols produce undesirable effects, such as tailing and excessive retention in RP separations, although there have been cases reported where the untreated silanols improve such separations. The concentration of the unbonded silanols in nonpolar bonded phases is normally reduced by the process of end... [Pg.1176]

Of greater interest from a structural point of view are examples where CP and non-CP spectra differ. In the case of the hydrated phases of pure silica (silica gel and fumed silica), the intensities of the and peaks which are bonded to hydroxyl groups should be significantly increased by comparison with the Q" peak (unbonded silica). This was shown to be the case by Chuang and Maciel (1997) who used their Si results to refine a model of the silanol bonding at the surface of silica gel (Figure 4.17). The technique was also used in a study of gel synthesis of albite glass (Schmelz and Stebbins 1993). [Pg.228]

Size and shape of one of the fillers (HDPE) were changed to measure the effect on the strength. It was theorized that a fine-graded filler like HDPEfine (FM=2.24) with a large unbonded surface area would have a different effect on the strength than a large-sized filler like HDPEflake (FM=4.89) with less surface area. The tests were designed to determine this effect. [Pg.47]


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See also in sourсe #XX -- [ Pg.135 ]




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