A simple flow calorimeter

1962 ◽  
Vol 39 (7) ◽  
pp. 338
Author(s):  
Percy E. Pierce
Keyword(s):  
1977 ◽  
Vol 12 (1) ◽  
pp. 77-90
Author(s):  
J.F. Cordoba-Molina ◽  
P.L. Silveston ◽  
R. R. Hudgins

Abstract A simple Flow Model is proposed to describe the dynamic response of sedimentation basins. The response predicted by this model is linear as opposed to the real response of the basin which is nonlinear. However, the real response of the basin is highly correlated with its densimetric Froude number, and as a consequence our linear model effectively predicts the response of the basin in a restricted densimetric Froude Number range. Our experiments show that the response of the basin becomes more sluggish and erratic as the densimetric Froude number decreases.


Author(s):  
Timothy Aljoscha Frede ◽  
Marlene Dietz ◽  
Norbert Kockmann

AbstractFast chemical process development is inevitably linked to an optimized determination of thermokinetic data of chemical reactions. A miniaturized flow calorimeter enables increased sensitivity when examining small amounts of reactants in a short time compared to traditional batch equipment. Therefore, a methodology to determine optimal reaction conditions for calorimetric measurement experiments was developed and is presented in this contribution. Within the methodology, short-cut calculations are supplemented by computational fluid dynamics (CFD) simulations for a better representation of the hydrodynamics within the microreactor. This approach leads to the effective design of experiments. Unfavourable experimental conditions for kinetics experiments are determined in advance and therefore, need not to be considered during design of experiments. The methodology is tested for an instantaneous acid-base reaction. Good agreement of simulations was obtained with experimental data. Thus, the prediction of the hydrodynamics is enabled and the first steps towards a digital twin of the calorimeter are performed. The flow rates proposed by the methodology are tested for the determination of reaction enthalpy and showed that reasonable experimental settings resulted. Graphical abstract A methodology is suggested to evaluate optimal reaction conditions for efficientacquisition of kinetic data. The experimental design space is limited by thestepwise determination of important time scales based on specified input data.


2019 ◽  
Vol 282 ◽  
pp. 02056
Author(s):  
Miloš Jerman ◽  
Vratislav Tydlitát ◽  
Robert Černý

In this paper the reaction heat development of alkali activated aluminosilicates is studied by an isothermal heat flow calorimeter. The highest reaction activity is observed during two hours after mixing. The hydration heat power at early time is influenced mainly by the composition of tested mixtures involving ceramic dust as precursor and different amounts of sodium hydroxide and water glass as activators and by temperature.


SPE Journal ◽  
2016 ◽  
Vol 21 (04) ◽  
pp. 1470-1476 ◽  
Author(s):  
Ebrahim Hajidavalloo ◽  
Saeed Alidadi Dehkohneh

Summary When a blowout oil/gas well catches fire, usually a flow tube is used to detach the fire from the wellhead and provide appropriate conditions for operating team members to approach the well and install the blowout-preventer (BOP) cap. Using the flow tube above the wellhead creates powerful suction around the tube that may jeopardize the safety of crew members. To reduce the power of suction around the well, a new perforated flow tube instead of simple flow tube was introduced. To understand the effect of this new type of flow tube, modeling and simulation of the flow field around the blowout well were performed for both simple and perforated types of flow tube with Fluent 6.3.26 (2003) and Gambit 2.3.16 (2003) softwares. Different parameters around the well mouth were compared in both designs. The results showed that using the perforated flow tube decreases the vacuum around the well by 33% compared with the simple flow tubes. Thus, application of the perforated flow tube can be recommended in well-control operations for safety measures.


2006 ◽  
Vol 77 (2) ◽  
pp. 023105 ◽  
Author(s):  
Simon R. Bare ◽  
George E. Mickelson ◽  
Frank S. Modica ◽  
Andrzej Z. Ringwelski ◽  
N. Yang

1986 ◽  
Vol 163 ◽  
pp. 27-58 ◽  
Author(s):  
Laurence Armi

This is a theoretical and experimental study of the basic hydraulics of two flowing layers. Unlike single-layer flows, two-layer flows respond quite differently to bottom depth as opposed to width variations. Bottom-depth changes affect the lower layer directly and the upper layer only indirectly. Changes in width can affect both layers. In fact for flows through a contraction control two distinct flow configurations are possible; which one actually occurs depends on the requirements of matching a downstream flow. Two-layer flows can pass through internally critical conditions at other than the narrowest section. When the two layers are flowing in the same direction, the result is a strong coupling between the two layers in the neighbourhood of the control. For contractions a particularly simple flow then exists upstream in which there is no longer any significant interfacial dynamics; downstream in the divergent section the flow remains internally supercritical, causing one of the layers to be rapidly accelerated with a resulting instability at the interface. A brief discussion of internal hydraulic jumps based upon the energy equations as opposed to the more traditional momentum equations is included. Previous uniqueness problems are thereby avoided.


2013 ◽  
Vol 102 (16) ◽  
pp. 163110 ◽  
Author(s):  
S. Sadat ◽  
E. Meyhofer ◽  
P. Reddy

1993 ◽  
Vol 15 (4) ◽  
pp. 141-146 ◽  
Author(s):  
J. S. Cosano ◽  
M. D. Luque de Castro ◽  
M. Valcárcel

This paper describes a simple flow-injection (FI) manifold for the determination of a variety of species in industrial water. The chemical systems involved in the determination of ammonia (formation of Indophenol Blue), sulfate (precipitation with Ba(II)), and iron (complexation with 1,10-phenanthroline with the help of a prior redox reaction for speciation) were selected so that a common manifold could be used for the sequential determination of batches of each analyte. A microcolumn of a suitable ion exchange material was used for on-line preconcentration of each analyte prior to injection; linear ranges for the determination of the analytes at the ng/ml levels were obtained with good reproducibility. The manifold and methods are ready for full automation.


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