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Surface course material

With regard to the surface course material in all new construction or major maintenance works, the Highways Agency proposes the use of thin surface course system or thin [Pg.564]

The typical thickness of the thin surfacing is 25 to 40 mm (or 50 mm) and is made of asphalt concrete for very thin layer according to CEN EN 13108-2 (2008). [Pg.565]

In the case where PA (CEN EN 13108-7 2008) is to be used, the surface layer thickness should be 50 mm and the asphalt must be modified with polymer or fibre additive. Its contribution to the material design thickness is only 20 mm hence, an increase by 30 mm of the total asphalt thickness is necessary. Additionally, a 60 mm dense binder course is required to be laid beneath PA surfacing. [Pg.565]

More information for the above asphalts for surfacing, binder course and asphalt base can be found in Chapter 5. [Pg.565]


It is interesting to note that as of 2006 in England, PA is not recommended as a surface course material for new or old pavements. The main reasons were the premature failures observed in some projects and its high cost. [Pg.257]

Low surface energy substrates, such as polyethylene or polypropylene, are generally difficult to bond with adhesives. However, cyanoacrylate-based adhesives can be effectively utilized to bond polyolefins with the use of the proper primer/activa-tor on the surface. Primer materials include tertiary aliphatic and aromatic amines, trialkyl ammonium carboxylate salts, tetraalkyl ammonium salts, phosphines, and organometallic compounds, which are initiators for alkyl cyanoacrylate polymerization [33-36]. The primer is applied as a dilute solution to the polyolefin surface, solvent is allowed to evaporate, and the specimens are assembled with a small amount of the adhesive. With the use of primers, adhesive strength can be so strong that substrate failure occurs during the course of the shear tests, as shown in Fig. 11. [Pg.862]

Some investigators believe that the best course to follow in scratch hardness determination is to find the tangential force acting on the surface of material under test required to obtain a scratch of width b. In this case, hardness is expressed as the ratio of that force to the scratch cross-section or a magnitude proportional to it, or else as a quotient of the work necessary to produce the scratch and its volume. Proponents of this method (Yushkin, 1971) consider that scratch hardness tests in the present form play only a marginal role. Unlike Shreyner (1949), who contended that the results obtained under these methods are less accurate than those for mineral-bymineral scratch after Mohs, they accept that these tests have certain usefulness, but only of a complementary nature. The differences of opinion arise from the different approach to the question of accuracy of the method of determination itself, since as can readily be proved, a strict relationship exists between hardness defined as the ratio of load P to square of... [Pg.203]

Reducing the course material in size in a colloid mill or by means of ultrasonic waves generally does not lead to a higher distribution ratio, i.e. to smaller particles. As it is smaller particles tend to form larger ones under the influence of mechanical forces and due to the attraction between the particles. These problems are solved to a large extent when a surface active substance and possibly a solvent are added during the reduction process. [Pg.70]

The surface courses for the selected pavements were assumed to consist of either conventional asphaltic concrete with limestone aggregate, sulfur-asphalt concrete with beach sand aggregate, or recycled Boulder asphaltic concrete with sulfur. Material properties used as VESYS IIM input data for these four surface layers are listed in Table IV. [Pg.211]

The target PA composition should declare the materials by which the mixture is composed, the grading, the binder content and whether reclaimed asphalt or other additives are used. With respect to the use of reclaimed asphalt, it should not exceed, unless agreed upon, 10% by mass of total mixture if PA is for surface course and 20% by mass of total mixture if PA is for any other course. [Pg.259]

AASHTO M 147. 2012. Materials for aggregate and soil-aggregate sub-base, base and surface courses. Washington, DC American Association of State Highway and Transportation Officials. [Pg.485]

The total thickness of the flexible pavement structure, comprising the surface course, binder course and base, is obtained from the right-hand portion of the nomograph shown in Eigure 13.19, and it depends on the type of base material. [Pg.565]

This book covers a wide range of lectures given at the Short Summer Course celebrated at La Laguna University about the new trends in the modern characterization methods chemical, microscopies, thermal. X-ray, resonance and nuclear methos for ceramics, glasses and related materials. This book also looks also at the zeolite thermal characterization methods as well as the new approaches in new microscopies for the investigation of surfaces in materials. [Pg.245]

For relatively dilute systems containing surface-active materials (i.e., surfactants see Chapter 3), the concentration of adsorbed material can be calculated from the known amount of material present before adsorption and that present in solution after adsorption equihbrium has been reached. A wide variety of analytical methods for determining the solution concentration are available, and almost all have been used at one time or other. In surfactant systems, the use of the Gibbs equation and measurements of tr are experimentally simple and straightforward (with proper precautions, of course). The utility of a specific method will depend ultimately on the exact nature of the system involved and the resources available to the investigator. [Pg.202]

Each of the de.scribed tension devices has its place and purpose. Because slitting lines are required to handle a variety of materials and applications, in due course, both of the above concepts were married into a single design. This resulted in a unit that can process oily and slippery material using only the pads, dry surface-critical material using the rolls, and many in-between materials combining both in tandem. With the tandem operation, three control variables are available to the operator pad air pressure, roll nip pressure, and brake air pressure (see Fig. 8). [Pg.72]

Table S.3 Techniques for Studying Surface Structure and Composition (Ref Dillard, J.G., Microscopic Spectroscopic Studies in Adhesion , Adhesion Principles and Practice, Course Material Kent State University, May 1998)... Table S.3 Techniques for Studying Surface Structure and Composition (Ref Dillard, J.G., Microscopic Spectroscopic Studies in Adhesion , Adhesion Principles and Practice, Course Material Kent State University, May 1998)...
Improperly or insufficiently treated metal being prepared for bonding, may mean that scale and corrosion are not completely removed. Most of this type of surface lying material is only loosely attached to the metal surface and can, under load in service detach itself. The result, of course, is a partial delamination of the contact area for the rubber with the metal. Once this detachment has taken place there will a gradnal widening of the detached area usually accompanied by some corrosion. [Pg.321]

Standard specification for materials for sod-aggregate subbase, base, and surface courses... [Pg.278]

All fibers, even bleached ones, seem to have some resinous, hydrophobic material on their surfaces. This material is usually referred to as pitch. We have investigated a bleached sulphite pulp. To remove some of the pitch the pulp can be extracted with ethanol. If, on the other hand, the pulp is heat treated (105 °C 3 h) the pitch is believed to spread over the surface. We made partition experiments for fines fractions from these pulps. A bleached sulphite pulp is of course hydrophilic and all samples partition towards the dextran phase in the basal system. On addition of 0.2 ml 5% P-PEG the hydrophobicity index is 0 for the untreated fiber, for the ethanol extracted fines it is -9 and for the heat treated +5. These results are thus entirely in accordance with our expectations. [Pg.112]

The value of 17.5 is an extremely high value compared with conventional polymers, which range between 8 (PE) and 14 (PA). It is to be expected that even higher values for PAni may be found in the course of further studies, because we do not yet know the degree of the surface purity. We expect that low surface energy materials may have been adsorbed onto the surface, thereby lowering the real value to the level we found. We expect that we might have measured the surface tension of ad-... [Pg.499]

In Figure 1, the time course of the electrical conductivity (EC) of leaf diffusates (intact leaves of Fagus sylvatica immersed in H2O) is depicted. The curve is clearly bi-phasic with a steep increase of EC within the first 30 minutes, reflecting the dissolution of surface deposited materials. Afterwards, a steady-state increase in EC results from a continuous efflux of electrolytes - most probably by diffusion - into the medium. With the help of an average specific conductance of 0.071 yS cm per yeq L the steady-state efflux into H2O, derived from linear regression anlaysis of the dashed curve in Fig. 1, was calculated to approx. 0.9 peq g(f.w.)- h . As opposed to the diffusive pathway of efflux, 7.7 yeq g(f.w.) were calculated to be washed-off. [Pg.126]

The AET was used at standard tests of numerous structural materials, above all steels and cast iron, prepared are ceramic samples. Part of tested samples had qjecial sur ce layer treatments by laser, plasma nitridation and similar. Effect of special surface treatment the authors published already earlier [5,6]. In this contribution are summed up typical courses of basic dependencies, measured by the AET at contact loading. [Pg.63]

Clearly, it is important that there be a large contact angle at the solid particle-solution-air interface. Some minerals, such as graphite and sulfur, are naturally hydrophobic, but even with these it has been advantageous to add materials to the system that will adsorb to give a hydrophobic film on the solid surface. (Effects can be complicated—sulfur notability oscillates with the number of preadsoibed monolayers of hydrocarbons such as n-heptane [76].) The use of surface modifiers or collectors is, of course, essential in the case of naturally hydrophilic minerals such as silica. [Pg.476]

Students and instructors). Each chapter presents first the basic surface chemistry of the topic, with optional material in small print. Derivations are generally given in full and this core material is reinforced by means of problems at the end of the chapter. A solutions manual is available to instructors. It is assumed that students have completed the usual undergraduate year course in physical chemistry. As a text for an advanced course, the basic material is referenced to fundamental, historical sources, and to contemporary ones where new advances have been incorporated. There are numerous examples and data drawn from both the older and from current literature. [Pg.801]


See other pages where Surface course material is mentioned: [Pg.564]    [Pg.564]    [Pg.136]    [Pg.133]    [Pg.404]    [Pg.164]    [Pg.166]    [Pg.215]    [Pg.100]    [Pg.183]    [Pg.190]    [Pg.198]    [Pg.2]    [Pg.229]    [Pg.106]    [Pg.2708]    [Pg.268]    [Pg.73]    [Pg.314]    [Pg.268]    [Pg.105]    [Pg.237]    [Pg.229]    [Pg.86]    [Pg.155]    [Pg.64]    [Pg.151]    [Pg.370]    [Pg.693]   


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