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Die rotation

A Proton Gradient Drives die Rotation of Bacterial Flagella... [Pg.533]

Noji, H., Yasuda, R., Yoshida, M., and Kino.sita, K., 1997. Direct observation of die rotation 0fF2-ATPa.se. 386 299-302. [Pg.707]

Evaluation of die rotational components of the internal energy and entropy using the partition function of Eq. (10.19) gives... [Pg.363]

Speed of die rotation and gelatin ribbon thickness are two important machine conditions that are included in Table 5. The rationale of their selection is... [Pg.96]

Blend time to solubilize active ingredients Gelatin mass mix time and temperature Die rotation speed Gelatin ribbon thickness Relative humidity of encapsulation room Bulk assay Dissolution Average fill weight Dosage form assay Microbial content... [Pg.96]

A bloom strength determination is part of the acceptance criteria for each receipt of gelatin raw material. The bloom gelometer numbers range from 125 to 195 for the 12 lots, with a mean of 147. This number was compared to gelatin ribbon thickness and die rotation speed during encapsulation to ascertain whether lot-to-lot differences had to be compensated for. No relationship was found. [Pg.98]

Unlike the coat hanger flat film dies, no simple final film adjustment is possible by lip flexing. Consequently, the order of magnitude of thickness accuracy in tubular dies is 10% as compared to 5% in flat sheet and film dies. This larger margin of accuracy in blown film dies is compensated by die rotation, which permits the distribution of the thickness variation across the entire width of the product. [Pg.721]

Fig. 19. Coherent scatter computed tomography demonstrator set-up [37]. The Philips X-ray tube is located on the left side, opposite to the detector. The primary beam slit unit and die rotational stage can be seen... Fig. 19. Coherent scatter computed tomography demonstrator set-up [37]. The Philips X-ray tube is located on the left side, opposite to the detector. The primary beam slit unit and die rotational stage can be seen...
Given that die rotation of a-D-glucopyranose is +112.2, the rotation of /3-D-glucopyranose is +18.7, and the rotation of an equilibrium mixture of the two anomers is +52.7, calculate the percentages of each anomer present at equilibrium. [Pg.1094]

The shutdown is usually very simple. Procedures for shutdown without cleanout starts by stop feeding plastic into the plasticator and reduce all heat settings to the melt heat. Reduce the screw speed to 2 to 5 rpm, purging the plastic if requires into a water bucket or drum prior to reducing the melt heat. The screw rotation continues until no more plastic exits the die. Rotations of the screw stops resulting in the so-called pumping the screw dry of plastics. [Pg.242]

Figure 1 7.14 Examples of layer plastics based on four modes of die rotation... Figure 1 7.14 Examples of layer plastics based on four modes of die rotation...
The picture of the translation closely parallels die rotational picture. In this case the counterpart of the Anderson model is the random jump model (see Section VIII). An important theoretical prediction of the reduced model of Section FV is the deviation from Pick s law, which is firmly supported by experiment. Note that this deviation precisely depends on the fluctuating nature of the reduced model. On the other hand, the theoretical analysis of Chapter VI shows that this multiplicative fluctuation must be traced back to the nonlinear nature of the microscopic interaction, therby rendering plausible the appearance of non-Gaussian microscopic prop es. [Pg.317]

The kev feature in statistical mechanics is the partition function Just as the wave Eeparatiou of die rotational and vibiational modes may be problematic. If two energy ... [Pg.157]

The spin-lattice relaxation times Ti due to the quadrupole interaction mechanism can be ctmverted to die rotational correlation times T2R ui a simple maimer. In the extreme narrowing limit attained by nqnd molecular rotational motions, the spin-lattice relaxation rate 1/Tj forthe m nucleus with the spin 1=1 is expressed by... [Pg.150]

Various theories have been introduced to explain the relative movemoit. Huxley proposed that the myosin head changed its orientation after binding to actin (die "rotating-head" model). According to the helix-coil transition, the normally o-helical coiled-coil structure "melts" to a random coil conformation, which implies a reduction in length. Movements of the myosin tails, as well as conformation changes of the actin have also been considered. It now seems clear, however, that the force production takes place in or very near the myosin heads [22]. Furthermore, among the three different states of myosin - empty actin site, ATP bound to the actin site and ADP-Pi boimd to die actin site - aU of which can... [Pg.356]

Nach GL (5) kann die sterische Struktur der Alkylradikale aus ap ent-nommen werden, wenn sie feste, dimch einen Winkel 0 gekennzeichnete Konformationen einnehmen. Bei innerer Rotation um die Ca-C -Bindung ist der MeBwert von Up der Mittelwert von (5) fiber die Rotations-bewegung. Bei freier Rotation nimmt er Werte von 20—30 Oe an. [Pg.468]

Densification is accomplished by a 300 HP California Pellet Mill Model 7162-3. The pellets are formed by extrusion through nominally 3/8 inch diameter radial holes in a cylindrical die. Pressure is exerted on a "pad" of the material to be densified by rolls which have fixed shafts. The pellet die rotates about the pressure rolls. Pellet length is controlled by a "cut-off" knife positioned to clip the pellets as they exit the rotating die. The exiting material stream from the pellet mill is mechanically lifted to a pellet cooler, which discharges to a screen to remove under-size pellet pieces and fines. The fines and pieces are recycled to the pellet mill infeed system. Finished pellets are conveyed by high pressure air system to tank storage. [Pg.195]


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See also in sourсe #XX -- [ Pg.546 ]




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