Protection stalling

The resins have wide appHcation. In nonreinforced form they serve as insulating coatings for electrical coils (46—47). As fiber reinforced resins, they can be made by reaction injection mol ding into laminates, castings, and coatings (48—49). Fiber-reinforced resins are used in marine appHcations (recreational boats) automotive parts (50) bathroom countertops and shower stalls and tubs and more recendy as baUistic protection for military vehicles and aircraft. 

When the motor overheats, the thermostat opens, interrupting motorline current. Pilot thermostats mounted on the windings of larger motors trip the motor starter rather than interrupt line current. This method gives good protection for sustained overloads, but because of the thermal time lag between the copper winding and the thermostat it may not provide adequate protec tion for stalled conditions or severe overloads. 

Stalling or locked rotor protection. This is also detected by the prolonged starting time as well as overheating of the machine. It is possible that the machine was already under operation and hot when it had stalled. Under such a condition, the rotor operates at a high freqitency and is more vulnerable to damage. Since it is not possible to create a replica of the rotor, separate... 

To ensure a time long enough to disconnect the motor from its power supply when the motor is stalled, fE shall exceed 5 s. When current dependent protective devices are applied to initiate the disconnection, fE shall increase with decreasing ratios of starting current to rated current. 

Figure 5 Starting from natural mRNA, a cDNA library (A blue) is produced and like ribosomal display, the cDNA is transcribed into mRNA (B) with no stop codons. The 3 -end of each mRNA molecule is ligated to a short synthetic DNA linker (C) and sometimes a polyethyleneglycol spacer, which terminates with a puramycin molecule (small red sphere). The ligation is stabilized by the addition of psoralen (green clamp), which is photoactivated to covalently join both strands. Addition of crude polysomes or purified ribosomes (D) results in translation of the mRNA into protein, but the ribosome stalls at the mRNA-DNA junction. Since there are no stop codons, release factors cannot function and instead the puromycin enters the A-site of the ribosome (A). Because puramycin is an analog of tyrosyl-tRNA, the peptidyl transferase subunit catalyzes amide bond formation between the puromycin amine and the peptide carboxyl terminus, but is unable to hydrolyze the amide link (which should be an ester in tyrosyl-tRNA) to release the dimethyladenosine. The ribosome is dissociated to release the mRNA-protein fusion (E), which is protected with complementary cDNA using RT-PCR (F). The mRNA library can then be selected against an immobilized natural product probe (G), nonbinding library members washed away and the bound mRNA (H) released with SDS. PCR amplification of the cDNA provides a sublibrary (A) for another round of selection or for analysis/ sequencing.

Vatavuk, W.M. Klotz, W.L. Stallings, R.L. Carbon adsorbers. In EPA Air Pollution Cost Control Manual, 6th Ed. EPA-452-B-02-001 U.S. Environmental Protection Agency Research Triangle Park, NC, 2002 195-235. 

The determinations of the solubility can be carried out in various ways- One of the simplest methods, which also gives sufficiently accurate results when the temperature is not high or when the solvent is not very volatile, can be carried out in the following manner. The solid substance is finely powdered (in order to accelerate the process of solution), and placed in sufficient quantity along with the solvent in a tube carefully closed by a glass stopper the latter is protected by a rubber cap, such as a rubber finger-stall. The tube is then rotated in a thermostat, the temperature of which does not vary more than one or two-tenths of a degree, until saturation is pro-... 

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