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Required yield

With inereasing temperature the two-phase tie-line beeomes shorter and shorter until the two eonjugate phases beeome identieal at a eritieal point where the maximum and minimum in the isothemi have eoaleseed. Thus the eritieal point is defined as that point at whieh 8 p/Sk) and (S />/(3k ) are simultaneously zero, or where the equivalent quantities 8 AldV) ai d 8 AldV ) axe, simultaneously zero. These requirements yield the eritieal eonstants in temis of the eonstants R, a and b. [Pg.617]

The reactors were thick-waked stainless steel towers packed with a catalyst containing copper and bismuth oxides on a skiceous carrier. This was activated by formaldehyde and acetylene to give the copper acetyUde complex that functioned as the tme catalyst. Acetylene and an aqueous solution of formaldehyde were passed together through one or more reactors at about 90—100°C and an acetylene partial pressure of about 500—600 kPa (5—6 atm) with recycling as required. Yields of butynediol were over 90%, in addition to 4—5% propargyl alcohol. [Pg.106]

The yield in a chemical reaction determines the quantities of materials in the material balance. Assumed yields are used to obtain approximate exploratoiy estimates. In this case, possible ranges should be given. Firmer estimates require yields based on laboratoiy or, preferably, pilot-plant work. [Pg.855]

Carboxylic esters can be treated with ketones to give p-diketones in a reaction that is essentially the same as 10-118. The reaction is so similar that it is sometimes also called the Claisen condensation, though this usage is unfortunate. A fairly strong base, such as sodium amide or sodium hydride, is required. Yields can be increased by the catalytic addition of crown ethers. Esters of formic acid (R H) give P-keto aldehydes. Ethyl carbonate gives P-keto esters. [Pg.571]

It is worthwhile pointing out another issue at this juncture. The low molecular-mass selectors can be grafted onto the surface of mesoporous silica (usually equal to 10 nm pore diameter) in a relatively high molar selector concentration due to their restricted space requirements (yielding typical selector loadings of about 0.4mmolg CSPcorrespondingtoca. 1.3 p,molm ). As a consequence, arelatively... [Pg.6]

The elastic force is given by the sum of a mechanical force —dU/dq and a corresponding Brownian force. The form of the Brownian force may be inferred by requiring that Fa vanish when /( ) = v /eq( ). in order to guarantee that the probability flux 7 vanishes in thermal equilibrium. This requirement yields an elastic force... [Pg.84]

In the first case, we set up a hypothesis about the population and then either accept or reject it by a test using sample data. The first two examples in the first paragraph above involve hypothesis testing. In the first example, the hypothesis would be that the average yield equals the required yield. [Pg.23]

At the end of Chapter 1 (Section 1.5C) we indicated that cell enlargement requires yielding of the cell wall, an irreversible or plastic process that occurs when the internal hydrostatic pressure exceeds some critical or threshold value, />J,u.esh0id- This leads to another growth equation of the following form ... [Pg.94]

Boc derivatives of pyrroles.1 Base-sensitive pyrroles can be converted into the 1-Boc derivative by reaction with (Boc)20 in CH3CN or CH2C12 catalyzed by 4-dimethyl-aminopyridine. Triethylamine can be used as a base, but is not usually required. Yields are generally >80%. [Pg.159]

To determine the molecular structure, we must count the electron pairs around the sulfur atom. In each resonance structure the sulfur has one lone pair, one pair in a single bond, and one double bond. Counting the double bond as one pair yields three effective pairs around the sulfur. According to Table 13.8, a trigonal planar arrangement is required, yielding a V-shaped molecule ... [Pg.639]

Vehicles that exhibit the unusual property of Bingham-type plastic rheological flow are characterized by the need to overcome a finite yield stress before flow is initiated. Permanent suspension of most pharmaceutical systems requires yield-stress values of at least 2-5 Pa (20-50 dyn/cm ). Bingham plastic flow is rarely produced by pharmaceutical gums and hydrophilic colloids. National Formulary (NF) carbomers exhibit a sufficiently high yield value at low solution concentration and low viscosity to produce permanent suspensions. The carbomers, however, require a pH value between 6 and 8 for maximum suspension performance. The polymer is essentially incompatible... [Pg.3604]

For optimization purposes, it is convenient to use analytical 0.46 x 25-cm columns filled with the stationary phase available in bulk quantities for PHPLC. Primary evaluation and selection of the stationary and mobile phases, based on the selectivity of separation, column efficiency, and product retention, should be done initially on an analytical scale, including experiments under overload conditions on an analytical column. A particular set of chromatographic conditions includes the column, programmed mobile phase, flow rate, sample solution composition and amount injected, temperature, and collection points. These conditions are evaluated to obtain optimization of the maximum recovery of the desired material with required purity, or the maximum available purity for the required yield based on the HPLC analysis of collected fractions. [Pg.1260]

This requirement yields the following differential equations for the transformation matrix [55,57,58]... [Pg.283]

Azobenzenes are oxidized to azoxybenzenes when heated with 30% hydrogen peroxide in acetic acid at 65° or at the reflux temperature.- In some instances a reaction period of 24 hrs. is required. Yields are in the range 50-90%. [Pg.965]

It is advisable to carry out practical measurements in order to determine the amount of solvent required, yield and plate number for the process. See the literature [4-6] for further details. The selectivity of the solvent is of special importance with solid-liquid extraction. If the solute to be extracted is chemically uniform, the required solvent can be selected based on the similar polarity with the solutes. Table 2.1 provides further details. [Pg.18]

Desired batch size (required tank dimensions) based on required yield. [Pg.1127]

When security is considered later, this requirement yields the statement that any subset of the participants that includes the signer can carry out initialization successfully even if all the other participants try to disturb them. This is why initialization sometimes needs identities as output parameters If the structure of an implementation prescribes that more participants than the signer play an active part in initialization, they may always disrupt. Thus the best thing one can do is to detect disturbances and to finish initialization with fewer participants. In these cases, the users will want to know with whom initialization was finally successful. [Pg.87]


See other pages where Required yield is mentioned: [Pg.301]    [Pg.552]    [Pg.1122]    [Pg.78]    [Pg.23]    [Pg.153]    [Pg.462]    [Pg.199]    [Pg.90]    [Pg.30]    [Pg.303]    [Pg.213]    [Pg.552]    [Pg.1116]    [Pg.660]    [Pg.180]    [Pg.159]    [Pg.409]    [Pg.1455]    [Pg.1169]    [Pg.686]    [Pg.560]    [Pg.1400]    [Pg.883]    [Pg.419]    [Pg.222]    [Pg.106]    [Pg.122]    [Pg.454]   
See also in sourсe #XX -- [ Pg.43 ]




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