Of the Paper

What good is the best discovery if nobody knows about it Even more important than the discovery is the announcement of discovery. In science it so happens that the discoverer becomes known with the discovery, or his professor does in any case. This is what is motivating. You make a discovery official by writing a paper about it (Kramer 1994). 

The paper is the product of scientific work, and the papers of a researcher are the basis for the respect he enjoys among colleagues. A doctoral candidate, for example, must thus strive to write papers in graduate school. If this is not possible, she should at least appear as coauthor on the papers of others. However, it should be noted that number and quality of the papers do not necessarily correlate with the prospects for social promotion. At least the correlation has not been scientifically proven yet. The political and social circumstances of paper writing are described in Bar (1992). 

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Fischer projection A method of representing three-dimensional structures in two-dimensional drawings in which the chiral atom(s) lies in the plane of the paper. The two enantiomeric forms of glyceraldehyde are represented as... 

A fatal accident and some other disasters, which were caused by small cracks, lead to a more strict consideration of the security of these steam drums. Parallel to these the economical pressure, due to the globalisation of the today s industry, lead to the increase of the pressure and the rotation speed of the paper production machines for a higher output of the production, which means, that all safety aspects from the design and the material will be exploited totally. On the other hand cast iron is also not a ductile and comfortable material, like the most steels for the pressure equipment. 

This presentation will not attempt to present all these projects, but instead focus on the ongoing network activities and the available sources for further information through the Commission s information services, with the CORDIS database being the prime source of information (see details at the end of the paper). 

The second task is then analysing the results of the scan. The results can be displayed live on a display screen, or stored and presented all at once or after further scaling and analysis. This playback feature of sample data will be the subject of the remainder of the paper, for as we will see the playback need not be immediate nor on site, but could take place synchronously or asynchronously over the Internet. 

Most of the situations encountered in capillarity involve figures of revolution, and for these it is possible to write down explicit expressions for and R2 by choosing plane 1 so that it passes through the axis of revolution. As shown in Fig. II-7n, R then swings in the plane of the paper, i.e., it is the curvature of the profile at the point in question. R is therefore given simply by the expression from analytical geometry for the curvature of a line... 

The surface tensions for a certain cubic crystalline substance are 7100 = 160 ergs/cm, 7110 = 140 eigs/cm, and 7210 = 7120 = 140 ergs/cm. Make a Wulff construction and determine the equilibrium shape of the crystal in the xy plane. (If the plane of the paper is the xy plane, then all the ones given are perpendicular to the paper, and the Wulff plot reduces to a two-dimensional one. Also, 7100 = 7010. etc.)... 

Figure Bl.16.14. Top, the canonical axes for triplet naphthalene. The z-axis is directed out of the plane of the paper. Bottom, energy levels and relative populations during the CIDEP triplet mechanism process. See text...

In this paper, we focus on numerical techniques for integrating the QCMD equations of motion. The aim of the paper is to systematize the discussion concerning numerical integrators for QCMD by ... 

Sometimes the crude substance may contain an insoluble impurity, and on cooling the solution it may be difficult to judge how much of the solid matter is merely undissolved impurity and how much is solute which has subsequently crystallised from solution. To avoid this difficulty, the hot solution should be filtered, and should thus always be absolutely clear before cooling is attempted. Therefore filter the hot solution into a clean tube through a very small fluted filter-paper contained in a correspondingly small glass funnel, which should have had its stem cut off as that shown in Fig. 6, p. 12 (and for the same reason). Unless the upper part of the filter is cut awav to reduce its size to a minimum, a large proportion of the solution will remain held mechanically in the pores of the paper itself and only a few drops of clear filtrate will be obtained. 

The basin A is then gently heated by a small Bunsen flame, which should be carefully protected from side draughts by screens, so that the material in A receives a steady uniform supply of heat. The material vaporises, and the vapour passes up through the holes into the cold funnel C. Here it cools and condenses as fine crystals on the upper surface of the paper B and on the walls of C. When almost the whole of the material in A has vaporised, the heating is stopped and the pure sublimed material collected. In using such an apparatus, it is clearly necessary to adjust the supply of heat so that the crude material in A is being steadily vaporised, while the funnel C does not become more than luke warm. 

A drop of an aqueous solution of the mixture to be separated is now placed near the bottom of the paper strip and allowed to evaporate in the air. The strip is now again suspended in the closed cylinder, but with the bottom of the strip just immersed in the solvent. The capillary action of the paper will cause the solvent to rise steadily up the strip, and during this process the solvent, which now contains the mixture in solution, is continuously extracted by the retained water molecules in the paper. A highly hydrophobic (water-repellent) solute will move up closely behind the solvent-front, whereas a highly hydrophilic solute will barely leave the original point where the drop of the mixed solutes in solution has been dried. In an intermediate case,... 

Now place 35 ml. of the mixed solvent (C) in the clean cylinder E, and suspend the strip, as described above, to the horizontal arm of G (Fig. 25(A)) adjust the position of the strip so that, when the bung is firmly in position, the bottom of the paper-strip is about 5 mm. above the solvent. Place the cylinder for 5-8 hours in a draught-free place, such as a cupboard, where the temperature is reasonably constant. 

Now roll up the Carius tube (while still in a vertical position) in a strip of ordinary thick drying paper, and then place it in the heavy iron protector tube if the Carius tube is too short and tends to disappear within the iron tube, a short section of old glass tubing should first be placed in the iron tube so that the capillary of the Carius tube just projects. The function of the paper is to protect the Carius tubing from being scratched, and also (more important) to prevent the local overheating which would otherwise occur at places where the Carius tube is in direct contact with the iron tube. The sealed tube, throughout its manipulation, should be left as nearly vertical as possible, so that the contents do not leave the rounded end. 

Sulphur. Moisten the centre of a filter paper with sodium plumbite solution. Add about 10 ml. of dilute hydrochloric acid to the residue in the dish and immediately cover it with the prepared filter paper. If zinc sulphide is present in the residue, a dark brown stain, visible on the upper surface of the paper, will be obtained frequently the presence of hydrogen sulphide can also be detected by its odour. 

It is the purpose of this and the following chapter to report the quantitative data concerning the relationship of structure to orientation and reactivity in aromatic nitration. Where data obtained by modern analytical methods are available they are usually quoted in preference to the results of older work. Many of the papers containing the latter are, however, noted in the brief discussion which is given of interpretations of the results. 

When using Fischer projections for this purpose however be sure to remember what three dimensional objects they stand for One should not for example test for superim position of the two chiral stereoisomers by a procedure that involves moving any part of a Fischer projection out of the plane of the paper in any step... 

End views of the quadrupole assembly (a) showing the theoretically desired cross-section and (b) illustrating the practical system. In (b), a positive potential, +(U + Vcoscot), is applied to two opposed rods (A) and a negative potential, -(U + Vcoscot), to the other two (B). The dotted lines indicate planes of zero electric field. The dimension (r) is typically about 5 mm with rod diameters of 12 mm. The x- and y-axes are indicated, with the z-axis being perpendicular to the plane of the paper. 

CeUulose is the most abundant polymer, an estimated 10 t being produced aimuaUy by natural processes. SuppUes for the rayon industry can be obtained from many sources, but in practice, the wood-pulping processes used to supply the needs of the paper and board industries have been adapted to make the necessary speciaUy pure grade. Of the 3 x 10 t of wood used by the paper and board industry (13) in 1989, about 6 x 10 t were purified to provide the 2.5 x 10 t of dissolving pulp required by the viscose processes. 

E. Hamilton and B. Leopold, eds.. Pulp and Paper Manufacture, Vol. 3, Secondary Fibers and Non-Wood Pulping, Joint Textbook Committee of the Paper Industry, Tappi, Adanta, Ga., 1987. 

Fluidyibsorbamy. Fluids like ink penetrate into paper during the printing process. The further the ink penetrates, the less glossy the print. The degree of penetration in paper is generally a function of the paper porosity and wettabiUty by the fluid. It can be controlled by the particle size, shape, and chemical nature of the filler or filler surface. In particular, plate-like fillers, such as clays, tend to produce the best fluid holdout because they tend to overlap and reduce the porosity at the paper surface (see Inks). 

R. Smith and T. Norris, eds., TAPPI Proceedings 1988 Paper Preservation Symposium, Technical Association of the Paper and Pulp Industry, Washington, D.C., 1988. 

D. Clayton and co-workers, "Chemistry of Alkaline Pulpiag," ia Eulp and Paper Manufacture, 3rd ed., Vol. 5, Alkaline Pulpiag, The Joiat Textbook Committee of the Paper Industry, TAPPI, CPPA, Technology Park Adanta, Ga., 1989. 

Terpenes, specifically monoterpenes, are naturally occurring monomers that are usually obtained as by-products of the paper and citms industries. Monoterpenes that are typically employed in hydrocarbon resins are shown in Figure 2. Optically active tf-limonene is obtained from various natural oils, particularly citms oils (81). a and P-pinenes are obtained from sulfate turpentine produced in the kraft (sulfate) pulping process. Southeastern U.S. sulfate turpentine contains approximately 60—70 wt % a-pinene and 20—25 wt % P-pinene (see Terpenoids). Dipentene, which is a complex mixture of if,/-Hmonene, a- and P-pheUandrene, a- and y-terpinene, and terpinolene, is also obtained from the processing of sulfate Hquor (82). 

Two processes precede the affixing of the heads for wooden matches. The first one is glow-proofing of the splint by impregnation with ammonium phosphate or a mixture of it with boric acid. In paper matches, the impregnation is conveniently done during the fabrication of the paper. This suppresses... 

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