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Base-lines

The time taken to complete a base line study and EIA should not be underestimated. The baseline study describes and inventorises the natural initial flora, fauna, the aquatic life, land and seabed conditions prior to any activity. In seasonal climates, the baseline study may need to cover the whole year. The duration of an EIA depends upon the size and type of area under study, and the previous work done in the area, but may typically take six months. The EIA is often an essential step in project development and should not be omitted from the planning schedule. [Pg.71]

A more sophisticated and increasingly popular method of on-condItion maintenance is to monitor the performance of equipment on-line. For example, a piece of rotating equipment such as a turbine may be monitored for vibration and mechanical performance (speed, inlet and outlet pressure, throughput). If a base-line performance is established, then deviations from this may indicate that the turbine has a mechanical problem which will reduce its performance or lead to failure. This would be used to alert the operators that some form of repair is required. [Pg.289]

It is no longer acceptable in most countries to treat decommissioning as an issue that can be ignored until the end of a project. Increasingly operators are being required to return industrial sites to their original condition after use. Many operators now perform a base line survey before they build on an area so that the impact of operations can be quantified, and in some cases so that they are not held responsible for the pollution of previous site owners. [Pg.371]

Fig. 7. Continuous process for solvent-extmded single-base propellant (automated single-base line). Vey = conveyor. Fig. 7. Continuous process for solvent-extmded single-base propellant (automated single-base line). Vey = conveyor.
After a suitable number of pulses have been acquired, the time-domain spectmm is transformed into a frequency-domain spectmm and phased so that the base line of the spectmm is fiat and the peaks all fall on the same (positive) side of the base line. Information obtainable from this spectmm includes chemical shifts, coupling constants, and integrated peak areas. [Pg.402]

Adding the real experimental base line to the result date to get experimental series. [Pg.30]

Whenever you have to report on the structure of an alloy - because it is a possible design choice, or because it has mysteriously failed in service - the first thing you should do is reach for its phase diagram. It tells you what, at equilibrium, the constitution of the alloy should be. The real constitution may not be the equilibrium one, but the equilibrium constitution gives a base line from which other non-equilibrium constitutions can be inferred. [Pg.25]

Alloys can exist in non-equilibrium states - the Al-Cu example was an illustration. But it is always useful to know the equilibrium constitution. It gives a sort of base-line for the constitution of the real alloy, and the likely non-equilibrium constitutions can often be deduced from it. [Pg.325]

The turbine undergoes three basic tests, these are hydrostatic, mechanical, and performance. Hydrostatic tests are to be conducted on pressure-containing parts with water at least one-and-a-half times the maximum operating pressure. The mechanical run tests are to be conducted for at least a period of four hours at maximum continuous speed. This test is usually done at no-load conditions. It checks out the bearing performance and vibration levels as well as overall mechanical operability. It is suggested that the user have a representative at this test to tape record as much of the data as possible. The data are helpful in further evaluation of the unit or can be used as base-line data. Performance tests should be conducted at maximum power with normal fuel composition. The tests should be conducted in accordance with ASME PTC-22, which is described in more detail in Chapter 20. [Pg.163]

Performance maps These are performanee maps based on design or initial tests (base lines) of the various maehinery parameters. These maps, for example present how power output varies with ambient eonditions, or with properties of the fuel, or the eondition of the filtration system or how elose to the surge line a eompressor is operating. On these maps, the present value is displayed, thus allowing the operator to determine the degradation in performanee oeeur-ring in the units. [Pg.650]

It is very important to form a base line for the entire power plant. This would enable the operator to determine if the seetion of the plant is operating below design eonditions. The following performanee eurves should be obtained either from the manufaeturer or during aeeeptanee testing so that the in-depth study of the parameters and their interdependeney with eaeh other ean be defined ... [Pg.706]

Bacteriophage repressor proteins provide excellent examples of sequence-specific interactions between the side chains of a protein and bases lining the floor of the major groove of B-DNA. As we shall see, to fit the protein s recognition module into this groove it has to be made even wider in other words, the B-DNA has to be distorted. [Pg.125]

Tangents Method. The tangents on either side of the peak are drawn through the inflection points until the baseline. For an ideal Gaussian peak the resulting base line interval Wi, is equal to 4or. Equation (1) becomes with the width (Wb) ... [Pg.432]

Grundlinie,/. ground line, base line, basis outline. [Pg.196]

The observation of the spectrum for styrene polymerized on the surface of silane-treated silica and of the difference spectrum of polystyrene adsorbed on the surface of silica have revealed that there are absorption bands of atactic polystyrene at 1602, 1493, 1453, 756, and 698 cm. The absorption bands at 1411 and 1010 cm are related to vinyl trimethoxy silane, and C of the difference spectrum is below the base line. This indicates that the vinyl groups of silane react with styrene to form a copolymer. [Pg.827]

To use central differences, the origin of x must be shifted to a base line (shaded area in Table 1-13) and x rescaled so one full (two half) line spacing = 1 unit. Sterling s formula (full lines as base) is defined as... [Pg.65]

Central Difference Table with Base Line... [Pg.66]

Post-exposure techniques are well documented for a variety of metals (ASTM and NACE). A disadvantage of coupon techniques is that the response to severe corrosion that may occur for short periods of time is not detected because the response measured is only an average for the period of exposure, although coupons can be withdrawn at intervals of time provided a sufficient number are placed at the start of exposure. The important aspect of coupons is that data obtained from their use can be used as base-line and therefore can be used to correlate corrosion data from other methods. [Pg.1135]

Fig. 4.8.3 Absorption spectra of pure mineopsin-2 (A), its luminescence product after the addition of Ca2+ (B), and the base line (C). Sample concentration 0.081 mg/ml. From Ward and Seliger, 1974b, with permission from the American Chemical Society. Fig. 4.8.3 Absorption spectra of pure mineopsin-2 (A), its luminescence product after the addition of Ca2+ (B), and the base line (C). Sample concentration 0.081 mg/ml. From Ward and Seliger, 1974b, with permission from the American Chemical Society.
Fig. 6.2.4 Change in the absorption spectrum of pholasin (14.5 p,M) caused by the luminescence reaction catalyzed by Pholas luciferase (1.1 p.M). The curve shown is the differential spectrum between a cell containing the mixture of pholasin and Pholas luciferase (0.9 ml in the sample light path) and two cells containing separate solutions of pholasin and the luciferase at the same concentrations (in the reference light path), all in 0.1 M Tris-HCl buffer, pH 8.5, containing 0.5 M NaCl. Four additions of ascorbate (3 iM) were made to the sample mixture to accelerate the reaction. The spectrum was recorded after 120 min with a correction for the base line. From Henry and Monny, 1977, with permission from the American Chemical Society. Fig. 6.2.4 Change in the absorption spectrum of pholasin (14.5 p,M) caused by the luminescence reaction catalyzed by Pholas luciferase (1.1 p.M). The curve shown is the differential spectrum between a cell containing the mixture of pholasin and Pholas luciferase (0.9 ml in the sample light path) and two cells containing separate solutions of pholasin and the luciferase at the same concentrations (in the reference light path), all in 0.1 M Tris-HCl buffer, pH 8.5, containing 0.5 M NaCl. Four additions of ascorbate (3 iM) were made to the sample mixture to accelerate the reaction. The spectrum was recorded after 120 min with a correction for the base line. From Henry and Monny, 1977, with permission from the American Chemical Society.
Every column (including chemically bonded columns) will have some column bleed. The amount of column bleed will increase with increasing column temperature, film thickness, column diameter, and column length. The base line starts to rise approximately 25-50° below the upper temperature limit of the stationary phase. After a column is installed in a GC/MS system, a background spectrum should be obtained for future reference. [Pg.362]

A different design approach is used in this case. Instead of assuming an apparent modulus of elasticity using a constant creep situation covering the life of the chair, it is better to determine the actual creep deflection over a typical stress cycle, the creep recovery over a non-use cycle, and so on until the creep is determined after a series of what might be considered typical hard usage cycles for the chair. The accumulated creep after a period of two weeks can be assumed to represent the base line for an apparent modulus of elasticity to determine the design life of the chair. [Pg.250]

Case I. i3 = oti2- The tie lines are parallel to the 2-3 binary base line. [Pg.201]

A thermogram from a differential scanning calorimeter. The peak indicates a phase change in the sample, and the difference in base line before and after the phase transition is due to the difference in heat capacities of the two phases. [Pg.360]

The peak height is taken as the distance between the extended base line beneath the peak and the peak maximum. The peak height, under certain conditions, will be proportional to the mass of solute present in the peak and can, thus, be used in quantitative analysis. However, the most common measurement employed in quantitative analysis is the peak area. [Pg.12]


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Base line absorbance

Base line compensator

Base line correction

Base line determination

Base line extrapolation

Base line, accurate

Base line, instability

Base line,definition

Base-line method

Base-line shifts

Central difference with base line

Drifts of the base line

Infrared spectroscopy base-line measurement method

Measured base line

Narcosis base-line toxicity

Neural Network-Based Optimizing Controller With On-Line Adaptation

On-line Coupling of MS-based Cathepsin B Assay to HPLC

Single-base line process

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