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Branches, small

Forest residues typically refer to those parts of trees such as treetops, branches, small-diameter wood, stumps and dead wood as well as undergrowth and low-value species. The conversion of wood to biofuels and biochemicals has long been a goal of the forest products industry. Forest residues alone count for some 50% of the total forest biomass and are currently left in the forest to rot (Demirbas, 2001). [Pg.48]

The spleen functions as a large lymph node and is supplied with blood via a single artery which progressively divides into smaller branches. Small arterioles are surrounded by areas of lymphocytes, which are known as the white pulp of the spleen. The arterioles ultimately end in vascular sinusoids, which contain different types of cells but especially erythrocytes, hence forming the red pulp of the spleen. [Pg.404]

Artillery Ammo Branch Research Materials Branch Ammo Development Branch Artillery Development Branch Small Arms Development Branch Tank and Automotive Branch Guided Missiles Branch Executive Branch... [Pg.761]

Ericoidsi densely branched, small-leaved, usuallylow under-... [Pg.39]

In the formation of microporous membranes from gels the building units are usually more or less branched, small silica molecules which can interpenetrate... [Pg.275]

Calibration for the methyl absorption based on mass spectrometric studies of such gaseous products produced during electron bombardment of polyethylene has demonstrated irradiation-induced detachment of complete alkyl units [15]. In addition to saturated alkanes characteristic of the branches, small quantities of methane, other paraffins, and olefins were simultaneously evolved. It was suggested that extraneous paraffins result from cleavage of the main chain [15,16]. Nerheim [17] has described a circular calibrated polymethylene wedge for the compensation of CH2 interferences in the determination of methyl groups in polyethylene by IR spectroscopy. [Pg.355]

A calibration for the methyl absorption based on mass spectrometric studies of such gaseous products produced during electron bombardment of polyethylene has demonstrated irradiation-induced detachment of complete alkyl units [10]. In addition to saturated alkanes characteristic of the branches, small quantities of... [Pg.382]

Figure Bl.4.9. Top rotation-tunnelling hyperfine structure in one of the flipping inodes of (020)3 near 3 THz. The small splittings seen in the Q-branch transitions are induced by the bound-free hydrogen atom tiiimelling by the water monomers. Bottom the low-frequency torsional mode structure of the water duner spectrum, includmg a detailed comparison of theoretical calculations of the dynamics with those observed experimentally [ ]. The symbols next to the arrows depict the parallel (A k= 0) versus perpendicular (A = 1) nature of the selection rules in the pseudorotation manifold. Figure Bl.4.9. Top rotation-tunnelling hyperfine structure in one of the flipping inodes of (020)3 near 3 THz. The small splittings seen in the Q-branch transitions are induced by the bound-free hydrogen atom tiiimelling by the water monomers. Bottom the low-frequency torsional mode structure of the water duner spectrum, includmg a detailed comparison of theoretical calculations of the dynamics with those observed experimentally [ ]. The symbols next to the arrows depict the parallel (A k= 0) versus perpendicular (A = 1) nature of the selection rules in the pseudorotation manifold.
Direct addition of ammonia to olefmic bonds would be an attractive method for amine synthesis, if it could be carried out smoothly. Like water, ammonia reacts with butadiene only under particular reaction conditions. Almost no reaction takes place with pure ammonia in organic solvents. The presence of water accelerates the reaction considerably. The reaction of aqueous ammonia (28%) with butadiene in MeCN in the presence orPd(OAc)i and PhjP at 80 C for 10 h gives tri-2,7-octadienylamine (47) as the main product, accompanied by a small amount of di-2,7-octadienylamine (46)[46,47], Isomeric branched... [Pg.430]

The small differences m stability between branched and unbranched alkanes result from an interplay between attractive and repulsive forces within a molecule (intramo lecular forces) These forces are nucleus-nucleus repulsions electron-electron repul sions and nucleus-electron attractions the same set of fundamental forces we met when... [Pg.86]

The ease of locating Point B depends on the shape of the knee of the isotherm.If the knee is sharp, corresponding to a high value of c. Point B can be located with accuracy even if the linear branch of the isotherm is short (see Fig. 2.10, curve (i)). When the knee is rounded, when c is small, Point B becomes difficult to locate, and the estimated value of rig may then differ widely from the BET monolayer capacity n . As will be seen shortly it is doubtful, indeed, how far isotherms in which Point B cannot be identified easily should be used for the estimation of monolayer capacity from either Point B or the BET plot. In practice, this reservation would include all isotherms having a value of c below 20. [Pg.56]

The molecules used in the study described in Fig. 2.15 were model compounds characterized by a high degree of uniformity. When branching is encountered, it is generally in a far less uniform way. As a matter of fact, traces of impurities or random chain transfer during polymer preparation may result in a small amount of unsuspected branching in samples of ostensibly linear molecules. Such adventitious branched molecules can have an effect on viscosity which far exceeds their numerical abundance. It is quite possible that anomalous experimental results may be due to such effects. [Pg.127]

The approximate symmetry of the band is due to the fact that Bi — Bq, that is, the vibration-rotation interaction constant (Equation 5.25) is small. If we assume that B = Bq = B and neglect centrifugal distortion the wavenumbers of the i -branch transitions, v[i (J)], are given by... [Pg.149]

The separation of individual lines within the Q branch is small, causing the branch to stand out as more intense than the rest of the band. This appearance is typical of all Q branches in infrared spectra because of the similarity of the rotational constants in the upper and lower states of the transition. [Pg.178]


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See also in sourсe #XX -- [ Pg.176 ]




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