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Short-Term Model

Both the mixing process and the approximation of the product profiles establish nonconvex nonlinearities. The inclusion of these nonlinearities in the model leads to a relatively precise determination of the product profiles but do not affect the feasibility of the production schedules. A linear representation of both equations will decrease the precision of the objective but it will also eliminate the nonlinearities yielding a mixed-integer linear programming model which is expected to be less expensive to solve. [Pg.153]

As indicated above, the variables representing the product specific holdups e R+ Vn, s and the product specific feeds e R+Vn N - 1, s as well as the equality constraints defining the total feed and the total holdup and the mixing process constraints are dropped. For ease of notation, the constraints which approximate the product profiles are substituted by an identity  [Pg.153]

The product specific quantities in the product balances around the mixing vessels are summed up and replaced by the total quantities, resulting in the following total balances of the mixing vessels  [Pg.153]

The timings of the supporting points of the storage profiles are shifted by another processing time, namely that of the approximated mixing process dM (see [Pg.153]

The height of a step of the product amount at is given by the yield pu leading to [Pg.154]


The short-term model can then be used to estimate resulting concentrations during specific periods or to estimate concentrations for suspected adverse meteorological conditions, so that changes can be incorporated in... [Pg.239]

The formulation of the engineered nonlinear short-term model presented is a variant of an MINLP model described in the dissertation by Schulz [5], In this subsection, all necessary indices, parameters and variables are introduced, and the constraints and the objective function are derived. In the following section, the nonlinear formulation is linearized yielding a MILP model. In order to keep track of the variables used in the MINLP and in the MILP formulation, they are displayed in Figure 7.3 along with some key parameters. [Pg.146]

In the experimental evaluation of substances for carcinogenesis based on experimental results of studies in a nonhuman species at some relatively high dose or exposure level, an attempt is made to predict the occurrence and level of tumorogenesis in humans at much lower levels. In this chapter we will examine the assumptions involved in this undertaking and review the aspects of design and interpretation of traditional long-term (lifetime) animal carcinogenicity studies as well as some alternative short-term models. [Pg.297]

Stone EC, McCracken MS, Kanerva RL, et al Development of a short-term model of decalin inhalation nephrotoxicity in the male rat. Food Chem Toa-zVo/25 3541-3547, 1987... [Pg.206]

Finally, aH photogenotoxic tests do not have a corresponding in vivo model, which raises the questionhowpositive iw vitro results couldbe clarified. There is anurgent need for development of suitable, short-term models that may validate positive in vitro data. [Pg.486]

One commonly used suite of models that is based on Gaussian plume modeling is the Industrial Source Complex (ISC) Dispersion Models (US EPA, 1995). This suite includes both a short-term model (ISCST), which calculates the hourly air pollutant concentrations in an area surrounding a source, as well as a long-term model (ISCLT), which calculates the average air pollutant concentrations over a year or longer. ISCLT uses meteorological data summarized by frequency for 16 radial sectors (22.5° each) this data format is referred to as a stability array (STAR). Within each sector of STAR, joint frequencies of wind direction, wind speed, and atmospheric stability class are provided. [Pg.346]

Foster DJ, Good DC, Fowlkes A, Sawaki L (2006) Atomoxetine enhances a short-term model of plasticity in humans. Arch Phys Med Rehabil 87 216-221. [Pg.182]

Figure 3. The diauxic growth curve predicted by Kampala s short term model. AG (glucose) = 90.0 AX (xylose) = 60.0. Figure 3. The diauxic growth curve predicted by Kampala s short term model. AG (glucose) = 90.0 AX (xylose) = 60.0.
The pathogenesis of pulmonaiy tumors induced by a tobacco carcinogen, 4-(methylnitrosamino)-l-(3-pyridyl)-l-butanone (NNK), and its inhibition by black tea was characterized in female A/J mice (Yang et al., 1997). In this short-term model, the administration of black tea polyphenols (0.3%) through the drinking water significantly inhibited NNK-induced early bronchiolar cell proliferation, as measured... [Pg.480]

Clearly it would be of immense benefit to all those involved with adhesives technology if the long-term service-life of bonded joints and components could be reliably predicted from short-term models. However, to predict accurately the service-life from short-term models requires a knowledge of the mechanisms and kinetics of attack. [Pg.689]

If it is necessary to consider short-term (hours or days) impact, the model PAL (4) will do a superior simulation of the area sources and a similar simulation of any point sources as done by the ISCLT model. [Pg.239]

SCREEN can not explicitly determine maximum impacts from multiple sources, except for the procedure to handle multiple nearby stacks by merging emissions into a single "representative" stack. The reader is directed to the MPTER (Pierce and Turner, 1980) or ISC (EPA, 1995b) models on EPA s Support Center for Regulatory Air Models (SCRAM) Bulletin Board System (BBS) to model short-term impacts for multiple sources. With the... [Pg.298]

In addition to SCREENS, you can also download TSCREEN, VISCREEN, and CTSCREEN. TSCREEN is a screening model for determining maximum short-term impact from toxic releases. Click the filename to download the file. [Pg.328]

ISCST3 - Industrial Source Complex - Short Term This model is used in more detailed studies of maximum air quality impacts (Phase 3 - Refined Modeling Analysis). The purpose is to compute short term concentration or deposition values, from multiple sources, on specified locations (i.e., receptors). To download the file, click the filename. This is the latest version of the regulatory model ISCST3 (00101) which was released by U.S. EPA on April 27, 2000. The file ISCST.ZIP is 1.60 MB (Executable, Source, Test Cases). You can also download the ISCST3 model evaluation references. [Pg.329]

PAL (Point, Area and Line Source Algoridim Model) is a short-term Gaussian steady state algoridim diat estimates concentrations of stable pollutants from point, area and line sources. [Pg.385]

PEM (Pollution Episodic Model) is an urban scale air pollution model capable of predicting short-term average surface concentrations and deposition fluxes of two gaseous or particulate pollutants. [Pg.386]

When spills and releases of hazardous gases or liquids occur, the concentration of the hazardous material in the vicinity of the release is often the greatest concern, since potential health effects on those nearby will be determined by the concentration of the substance at the time of the acute exposure. There are many models of routine continuous discharges (e.g., discharges arising from leaky valves in chemical plants), but these carmot be applied to single episodic events. Research on the ambient behavior of short-term environmental releases and the development of models for concentration profiles in episodic releases are cmcial if we are to plan appropriate safety and abatement measures. [Pg.139]

A variety of data sources are available to inform interactive programs, including prospective data sets, retrospective databases, expert opinion, and unpub-lished/published literature. Time horizon, that is, the length of time into the future considered in the analysis over which costs and outcomes are projected, is very important here [26]. For example, if a clinical trial or the published literature only report short-term results for a chronic condition, the outcomes may come into question. This is where decision-analytic models may come... [Pg.580]

With few exceptions, models find in favour of newer compounds Qonsson and Bebbington, 1994 Le Pen et al, 1994 McFarland, 1994 Stewart, 1994 Einarson et al, 1995 Lapierre et al, 1995 Nuitjen et al, 1995 Montgomeiy et al, 1996). One study (CCOHTA, 1997) did make allowances for variations in practice and patient behaviour. The results indicated that in the short term treatment was likely to be more successful with an SSRI than with a TCA, but at a higher cost. However, when treatment dropout rates found in naturalistic studies were substituted for drop-out rates found in controlled trials, the cost differences became smaller. When cost-utility analysis was applied, this increased cost was offset by improvements in quality of life for the patients. [Pg.47]

Of course, the term proven efficacy is central to any resource investment in this area. Basic information on time and dose responses in humans to complex foods rich in carotenoids (and other phytochemicals) is pitifully small. Much of our information is based upon inadequate databases derived from chemical analysis, in vitro models that have not been properly evaluated or validated, and short-term, high-dose human studies. Future research progress requires much more rigorous debate on the experimental systems employed... [Pg.123]


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