RAMP addition

A credible accident without a scram, or any initiating event (with or without an identifiable source) without a scram is called hypothetical. In the class of hypothetical accidents are the flow coast-downs without scram, sudden loss of cooling, large ramp additions of reactivity from unknown sources, multiple simultaneous control rod blowout, and multiple simultaneous voiding of individual channels. 

The design of the slope compensation circuit is almost fairly qualitative and may eventually need to be adjusted at the breadboard stage. To estimate how much additional ramp voltage is needed to keep the power supply stable, one performs the following equation. Aj is the gain or step-down influences of the transformers between the output and the current sense pin. 

The components connected between the emitter-follower and the currentsensing filter capacitor can be thought of as a resistor divider. An additional 0.17 V needs to appear at pin 7 (through a 1K resistor) so the amount of current that must be contributed to that node is 0.17 V/1K which is 170 pA. The capacitive coupling of the PNP to pin 7 essentially centers the oscillator waveform upon the current ramp. So,... 

The use of hydrazone or enamine derivatives of ketones or aldehydes offers the advantage of stcreocontrol via chelated azaenolates. Extremely useful synthetic methodology, with consistently high anti selectivity, has been developed using azaenolates based on (S)- or (R)-l-amino-2-(methoxymethyl)pyrrolidine (SAMP or RAMP)51 58 (Enders method, see Section 1.5.2.4.2.2.3.). An example which illustrates the efficiency of this type of Michael addition is the addition of the lithium azaenolate of (5 )-l-amino-2-(methoxymethyl)pyrrolidine (SAMP) hydrazone of propanal (R = II) to methyl (E )-2-butenoate to give the nub-isomer (an 1 adduct) in 80% yield with a diastereomeric ratio > 98 2,... 

An excellent synthetic method for asymmetric C—C-bond formation which gives consistently high enantioselectivity has been developed using azaenolates based on chiral hydrazones. (S)-or (/ )-2-(methoxymethyl)-1 -pyrrolidinamine (SAMP or RAMP) are chiral hydrazines, easily prepared from proline, which on reaction with various aldehydes and ketones yield optically active hydrazones. After the asymmetric 1,4-addition to a Michael acceptor, the chiral auxiliary is removed by ozonolysis to restore the ketone or aldehyde functionality. The enolates are normally prepared by deprotonation with lithium diisopropylamide. 

The Enders method has also been used as a key step in the synthesis of optically active Ar-heterocycles. The use of cyclic 1,3-diketones for the preparation of the SAMP or RAMP lithium azaenolates is shown by the synthesis of substituted 4,6,7,8-tetrahydro-2,5(l//,3//)-quinolinediones 2. Michael addition of 1 with, for example, benzylidene propanedioates followed by removal of the auxiliary and lactamization gives 2 with > 98% ee201. 

Adipic acid, 219.2 g (1.5 mol), and 77.6 g (1.25 mol) of 1,2-ethanediol are weighed into a 500-mL glass reactor equipped with a mechanical stirrer, a nitrogen inlet, and a distillation head connected to a condenser and a receiver fiask. The reactor is placed in a salt bath preheated at 180°C and the temperature is dien raised gradually to 220°C (see note at end of procedure) until the greater part of water has been removed (3 h). The reactor is cooled down to 160°C and vacuum is applied slowly to ca. 0.07 mbar (30 min). Temperature is ramped to 220°C (see note below) at a rate of l°C/min and reaction is continued for an additional 90 min. At the end of reaction, the carboxylic acid endgroup content is close to 1.90 mol/kg. No purification of final polyester is carried out. 

H2TPR results (Flow rate of 5% H2 = 20cc/min, Ramp rate= lOtl/min) show that Sb modifies the catalyst surface reducibility. The hydrogen consumption on WO3 takes place above 500 °C. It is evident from TPR results that new surface species were formed by Sb addition. The population of such species, that is represented as the area under the new peak, increases with increasing Sb content with the maximum at Sb=0.4 and then decreases with further increasing Sb content. 

Desorption chemical ionisation (DCI) mass spectrometry has been used for detecting additives extracted from polymers [51,52] by a solvent as volatile as possible. To use the DCI probe, 1 -2 iL of the sample, in solution, are applied to the probe tip, composed of a small platinum coil, and after the solvent has been allowed to evaporate at room temperature, the probe is inserted into the source. The sample is then subject to fast temperature ramping. DCI does not seem to be the most suitable mass-spectrometric method for analysis of dissolved polymer/additive matrices, because ... 

DIP-ToFMS is theoretically another option for the separation of additives from polymer in dissolutions using a probe temperature ramp. However, the technique also allows direct handling of solid substrate material, which is even more convenient. The technique has profitably been used for the analysis of non-UV cured ink, revealing diluent, photo-initiator and polymer [54]. 

In connection with the square-wave technique, mention can be made of high-frequency polarography, also called radiofrequency polarography and developed by Barker53, in which a sinusoidal radio-frequency cu, (100kHz to 6.4 MHz) square-wave modulated at co2 (225 Hz) is superimposed on to the dc potential ramp as the wave form includes (apart from additional higher... 

Although TPD is a versatile and useful technique widely available within the surface-science community, it does have some limitations. For one, because the experiments are carried out under vacuum, they can only probe irreversible reactions no readsorption of the desorbing products is possible. In addition, as the temperature is ramped during detection, the surface temperature and the reaction rates become coupled in a way difficult to separate or control. Of particular importance here is the fact that as the reactions proceed and the products desorb, the surface coverages decrease, so the rates at higher temperatures correspond to the new lower surface concentrations. In order to overcome this problem, isothermal kinetic experiments have been carried out using molecular beams [22,23],... 

Additions of stabilized carbanions to imines and hydrazones, respectively, have been used to initiate domino 1,2-addition/cyclization reactions. Thus, as described by Benetti and coworkers, 2-subshtuted 3-nitropyrrolidines are accessible via a nitro-Mannich (aza-Henry)/SN-type process [165]. Enders research group established a 1,2-addition/lactamization sequence using their well-known SAMP/ RAMP-hydrazones 2-308 and lithiated o-toluamides 2-307 as substrates to afford the lactams 2-309 in excellent diastereoselectivity (Scheme 2.72) [166]. These compounds can be further transformed into valuable, almost enantiopure, dihydro-2H-isoquinolin-l-ones, as well as dihydro- and tetrahydroisoquinolines. 

The immobilized carbamates (40 pmol) were transferred to a sealable 96-well Weflon plate, and admixed with 10 pmol each of various primary or secondary amines dissolved in 400 iL of anhydrous toluene. After sealing, the plate was irradiated in a multimode microwave instrument, first generating a ramp to reach 130 °C within 45 min and then holding this temperature for an additional 15 min. After cooling, the resins were filtered with the aid of a liquid handler and the filtrates were concentrated to obtain the desired substituted ureas in good purity and reasonable yields. Anilines reacted rather sluggishly and 2-substituted benzyl carbamates afforded somewhat inferior results. 

Rieck and Bell/Mitchell and Vannice—Ce addition promotes WGS during methanation. Rieck and Bell351 examined 2%Pd/Si02 catalysts promoted with various lanthanides (La, Ce, Pr, Nd, and Sm) in the range 4.4-4.7%, among them, ceria, and carried out TPR (H2) and TPO (02) and H2 and CO TPD (He flow) experiments, along with TPSR experiments (H2 used instead of He). The catalysts were ramped at a rate of 1 °C per sec in a flow of 75 ccm H2 and 25 ccm CO. The authors observed that in addition to methanation, C02 was produced, and that the... 

Indium also has many of the characteristics that make Al and Ga very useful for such applications. Particularly important is its capacity to dissolve Si, Ge and several lanthanide and transition metals, producing highly reactive forms of the elements. Moreover In does not form binaries with Si and Ge and has a low-melting point. RNiGe2 compounds, for instance, were prepared from stoichiometric quantities of the components in fine powder mixed with a 10 fold quantity of In in alumina tubes. These, flame sealed in fused silica tubes, were slowly heated to 1000°C, held at this temperature for a few hours, ramped down to 850°C, held for an additional 4 days and finally cooled down to room temperature over the course of another 4 days. Compound isolation from the In excess was performed by centrifugation at 300°C through a coarse frit. Further purification was carried out by a 15-minute submersion and sonication in 6 M aqueous HC1 (Salvador et al. 2004). 

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