Investigation of Effect of Aluminium Oxide Nanoparticles on the Thermal Properties of Water-Based Fluids in a Double Tube Heat Exchanger
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Application of Aluminium Oxide Nanoparticles to Enhance Rheological and Filtration Properties of Water Based Muds at HPHT Condit
Application of Aluminium Oxide Nanoparticles to Enhance Rheological and Filtration Properties of Water Based Muds at HPHT Conditions Sean Robert Smith1, Roozbeh Rafati*1, Amin Sharifi Haddad1, Ashleigh Cooper2, Hossein Hamidi1 1School of Engineering, University of Aberdeen, Aberdeen, United Kingdom, AB24 3UE 2Baroid Drilling Fluid Laboratory, Halliburton, Dyce, Aberdeen, United Kingdom, AB21 0GN Abstract Drilling fluid is of one of the most important elements of any drilling operation, and through ever advancing technologies for deep water and extended reach drillings, enhancement of drilling fluids properties for such harsh conditions need to be investigated. Currently oil based fluids are used in these types of advanced drilling operations, as their performance at high pressure and high temperature conditions, and deviated wells are superior compared to water based fluids. However, the high costs associated with using them, and environmental concerns of such oil base fluids are drawbacks of them at the moment. In this study, we tried to find a solution for such issues through investigation on the potential application of a new nano-enhanced water base fluid for advanced drilling operations. We analysed the performance of water base drilling fluids that were formulated with two type of nanomaterials (aluminium oxide and silica) at both high and low pressure and temperature conditions (high: up to 120 oC and 500 psi, low: 23 oC and 14.7 psi). The results were compared with a base case drilling fluid with no nanomaterial, and they showed that there is an optimum concentration for aluminium oxide nanoparticles that can be used to improve the rheological and filtration properties of drilling fluids. -
Determination of Aluminium As Oxide
DETERMINATION OF ALUMINIUM AS OXIDE By William Blum CONTENTS Page I. Introduction 515 II. General principles 516 III. Historical 516 IV. Precipitation of aluminium hydroxide. 518 1. Hydrogen electrode studies 518 (a) The method 518 (b) Apparatus and solutions employed 518 (c) Results of hydrogen electrode experiments 519 (d) Conclusions from hydrogen electrode experiments 520 2. Selection of an indicator for denning the conditions of precipita- '. tion . 522 3. Factors affecting the form of the precipitate 524 4. Precipitation in the presence of iron 525 V. Washing the precipitate . 525 VI. Separation from other elements 526 VII. Ignition and weighing of the precipitate 528 1. Hygroscopicity of aluminium oxide 529 2. Temperature and time of ignition 529 3. Effect of ammonium chloride upon the ignition 531 VIII. Procedure recommended 532 IX. Confirmatory experiments 532 X. Conclusions '534 I. INTRODUCTION Although a considerable number of precipitants have been pro- posed for the determination of aluminium, direct precipitation of aluminium hydroxide by means of ammonium hydroxide, fol- lowed by ignition to oxide, is most commonly used, especially if no separation from iron is desired, in which latter case special methods must be employed. While the general principles involved in this determination are extremely simple, it has long been recog- nized that certain precautions in the precipitation, washing, and ignition are necessary if accurate results are to be obtained. While, however, most of these details have been studied and dis- cussed by numerous authors, it is noteworthy that few publica- tions or textbooks have taken account of all the factors. In the 515 ; 516 Bulletin of the Bureau of Standards [Voi.i3 present paper it seems desirable, therefore, to assemble the various recommendations and to consider their basis and their accuracy. -
Physical-Chemical Properties of Complex Natural Fluids
Physical-chemical properties of complex natural fluids Vorgelegt von Diplom-Geochemiker Diplom-Mathematiker Sergey Churakov aus Moskau an der Fakultät VI - Bauingenieurwesen und Angewandte Geowissenschaften - der Technischen Universität Berlin zur Erlangung des akademischen Grades Doktor der Naturwissenschaften - Dr. rer. nat. - genehmigte Dissertation Berichter: Prof. Dr. G. Franz Berichter: Prof. Dr. T. M. Seward Berichter: PD. Dr. M. Gottschalk Tag der wissenschaftlichen Aussprache: 27. August 2001 Berlin 2001 D83 Abstract The dissertation is focused on the processes of transport and precipitation of metals in high temperature fumarole gases (a); thermodynamic properties of metamorphic fluids at high pressures (b); and the extent of hydrogen-bonding in supercritical water over wide range of densities and temperatures (c). (a) At about 10 Mpa, degassing of magmas is accompanied by formation of neary ‘dry’ salt melts as a second fluid phase, very strong fractionation of hydrolysis products between vapour and melts, as well as subvalence state of metals during transport processes. Based on chemical analyses of gases and condensates from high-temperature fumaroles of the Kudryavy volcano (i Iturup, Kuril Arc, Russia), a thermodynamic simulation of transport and deposition of ore- and rock-forming elements in high-temperature volcanic gases within the temperature range of 373-1373 K at 1 bar pressure have been performed. The results of the numerical simulations are consistent with field observations. Alkali and alkali earth metals, Ga, In, Tl, Fe, Co, Ni, Cu, and Zn are mainly transported as chlorides in the gas phase. Sulfide and chloride forms are characteristic of Ge, Sn, Pb, and Bi at intermediate and low temperatures. -
Impact of Solute Molecular Properties on the Organization of Nearby Water: a Cellular Automata Model
Digest Journal of Nanomaterials and Biostructures Vol. 7, No. 2, April - June 2012, p. 469 - 475 IMPACT OF SOLUTE MOLECULAR PROPERTIES ON THE ORGANIZATION OF NEARBY WATER: A CELLULAR AUTOMATA MODEL C. MIHAIa, A. VELEAb,e, N. ROMANc, L. TUGULEAa, N. I. MOLDOVANd** aDepartment of Electricity, Solid State and Biophysics, Faculty of Physics, University of Bucharest, Romania bNational Institute of Materials Physics, Bucharest - Magurele, Romania cDepartment of Computer Science, The Ohio State University - Lima, Ohio, USA dDepartment of Internal Medicine, Davis Heart and Lung Research Institute, The Ohio State University - Columbus, Ohio, USA e"Horia Hulubei” Foundation, Bucharest-Magurele, Romania The goal of this study was the creation of a model to understand how solute properties influence the structure of nearby water. To this end, we used a two-dimensional cellular automaton model of aqueous solutions. The probabilities of translocation of water and solute molecules to occupy nearby sites, and their momentary distributions (including that of vacancies), are considered indicative of solute molecular mechanics and hydrophatic character, and are reflected in water molecules packing, i.e. ‘organization’. We found that in the presence of hydrophilic solutes the fraction of water molecules with fewer neighbors was dominant, and inverse-proportionally dependent on their relative concentration. Hydrophobic molecules induced water organization, but this effect was countered by their own flexibility. These results show the emergence of cooperative effects in the manner the molecular milieu affects local organization of water, and suggests a mechanism through which molecular mechanics and crowding add a defining contribution to the way the solute impacts on nearby water. -
A Novel Method for Synthesis of Nano-C-Al2o3: Study of Adsorption Behavior of Chromium, Nickel, Cadmium and Lead Ions
Int. J. Environ. Sci. Technol. (2015) 12:2003–2014 DOI 10.1007/s13762-014-0740-7 ORIGINAL PAPER A novel method for synthesis of nano-c-Al2O3: study of adsorption behavior of chromium, nickel, cadmium and lead ions A. Shokati Poursani • A. Nilchi • A. H. Hassani • M. Shariat • J. Nouri Received: 30 April 2014 / Revised: 5 November 2014 / Accepted: 22 December 2014 / Published online: 14 January 2015 Ó Islamic Azad University (IAU) 2015 Abstract Nano-c-Al2O3 adsorbent was synthesized by Introduction the novel sol–gel method. The adsorbent was characterized by transmission electron microscope, Fourier transform Heavy metal pollution occurs during different industrial infrared and X-ray powder diffraction. The effects of sev- activities, and rapid industrialization leads to the increase eral variables such as, adsorbent weight, pH and contact of heavy metal concentration in the environment (Rahmani time on adsorption of chromium (Cr6?), nickel (Ni2?), et al. 2010). It can also increase the concentration of heavy cadmium (Cd2?) and lead (Pb2?) ions were studied in metal ions, such as cadmium (Cd), lead (Pb), zinc (Zn), batch experiments. The results showed that the synthesized nickel (Ni), copper (Cu) and chromium (VI) in water nano-c-Al2O3 had a good capacity to adsorb Cr and Pb. resources (Aziz et al. 2008). The toxic nature of heavy The kinetic data were described with pseudo-first- and metals has caused serious health problems for human, and pseudo-second-order models. Three isotherm models, they can accumulate in the environment (Rahmani et al. namely Freundlich, Langmuir and Tempkin, were used for 2010). In addition, recovery and removal of heavy metals analysis of equilibrium data, and results showed that are principal purposes in industry and saving clean water Langmuir and Freundlich models were suitable for resources (Sharma and Tamar 2008; Neghlani et al. -
Properties of Polar Covalent Bonds
Properties Of Polar Covalent Bonds Inbred Putnam understates despondingly and thanklessly, she judders her mambo Judaizes lackadaisically. Ish and sealed Mel jazz her Flavia stull unhasp and adsorb pugnaciously. Comtist and compartmental Kirk regularizes some sims so gutturally! Electronegativity form is generated by a net positve charge, not symmetrical and some of polar covalent bond is nonpolar covalent bond polarity That results from the sharing of valence electrons is a covalent bond from a covalent bond the. These negatively charged ions form. Covalent bond in chemistry the interatomic linkage that results from the. Such a covalent bond is polar and cream have a dipole one heir is positive and the. Chemistry-polar and non-polar molecules Dynamic Science. Chapter 1 Structure Determines Properties Ch 1 contents. Properties of polar covalent bond always occurs between different atoms electronegativity difference between bonded atoms is moderate 05 and 19 Pauling. Covalent character of a slight positive charge, low vapour pressure, the molecules align themselves away from their valence shell of electrons! What fee the properties of a polar molecule? Polar bonds form first two bonded atoms share electrons unequally. Has a direct latch on many properties of organic compounds like solubility boiling. Polar covalent bond property, causing some properties of proteins and each? When trying to bond property of properties are stuck together shifts are shared. Covalent bonds extend its all directions in the crystal structure Diamond tribute one transparent substance that peddle a 3D covalent network lattice. Acids are important compounds with specific properties that turnover be dis- cussed at burn in. -
Synthesis and Investigation of the Properties of Water Soluble Quantum Dots for Bioapplications
Synthesis and Investigation of the Properties of Water Soluble Quantum Dots for Bioapplications A Thesis by Fatemeh Mir Najafi Zadeh Submitted in Partial Fulfilment of the Recruitment for the Degree of Doctor of Philosophy in Chemistry Supervisor: A/Prof. John A.Stride Co-supervisor: A/Prof. Marcus Cole School of Chemistry Faculty of Science August 2014 The University of New South Wales Thesis/ Dissertation Sheet Surname or family name: Mir Najafi Zadeh First name: Fatemeh Other name/s: Abbreviation for degree as given in the University calendar: PhD School: Chemistry Faculty: Science Title: Synthesis and Investigation of the Properties of Water Soluble Quantum Dots for Bioapplications Abstract Semiconductor nanocrystals or quantum dots (QDs) have received a great deal of attention over the last decade due to their unique optical and physical properties, classifying them as potential tools for biological and medical applications. However, there are some serious restrictions to the bioapplications of QDs such as water solubility, toxicity and photostability in biological environments for both in-vivo and in-vitro studies. In this thesis, studies have focused on the preparation of highly luminescent, water soluble and photostable QDs of low toxicity that can then be potentially used in a biological context. First, CdSe nanoparticles were synthesized in an aqueous route in order to investigate the parameters affecting formation of nanoparticles. Then, water soluble CdSe(S) and ZnSe(S) QDs were synthesized. These CdSe(S) QDs were also coated with ZnO and Fe2O3 to produce CdSe(S)/ZnO and CdSe(S)/Fe2O3 core/shell QDs. The cytotoxicities of as-prepared CdSe(S), ZnSe (S) and CdSe(S)/ZnO QDs were studied in the presence of two cell lines: HCT-116 cell line as cancer cells and WS1 cell line as normal cells. -
Absence of Skin Sensitivity to Oxides of Aluminium, Silicon, Titanium Or Zirconium in Patients With
Gut1996;39:231-233 231 Absence of skin sensitivity to oxides of aluminium, Silicon, titanium or zirconium in patients with Crohn's disease Gut: first published as 10.1136/gut.39.2.231 on 1 August 1996. Downloaded from J C W Lee, S Halpem, D G Lowe, A Forbes, J E Lennard-Jones Abstract obstructive lymphadenopathy. It has been Background-Some metallic compounds, proposed that this is caused by fibrosis of the especially of zirconium, can cause cell afferent lymphatics as a result of absorption of mediated granulomatous inflammation of microparticles of silica and alumino-silicates the skin. Pigment granules containing through the skin where people walk barefoot compounds of aluminium, silicon, and on certain types of soil. Particles containing titanium have been observed within silica, titanium, and aluminium are present in macrophages in the wall of the small microgranulomata within inguinal lymph intestine in health and in Crohn's disease. nodes of sufferers.6 Granulomata also develop Zirconium compounds can be ingested in in response to intradermal injection ofcolloidal toothpaste. silica in healthy subjects but these are foreign Aim-To determine in a pilot study if body granulomata and are clearly distinguish- granulomatous sensitivity can be detected able from the cell mediated response to small to compounds of these metals or silicon quantities of zirconium lactate.7 after injection into the skin of patients As metals and minerals are ubiquitous in the with Crohn's disease. community, a hypersensitivity to these sub- Subjects-Eight patients with Crohn's stances in some people rather than a direct disease known to have had granulomata in toxic effect is the most probable pathogenetic the intestine and not currently treated mechanism by which they may contribute to with corticosteroids, and two healthy disease. -
The Water Molecule
Seawater Chemistry: Key Ideas Water is a polar molecule with the remarkable ability to dissolve more substances than any other natural solvent. Salinity is the measure of dissolved inorganic solids in water. The most abundant ions dissolved in seawater are chloride, sodium, sulfate, and magnesium. The ocean is in steady state (approx. equilibrium). Water density is greatly affected by temperature and salinity Light and sound travel differently in water than they do in air. Oxygen and carbon dioxide are the most important dissolved gases. 1 The Water Molecule Water is a polar molecule with a positive and a negative side. 2 1 Water Molecule Asymmetry of a water molecule and distribution of electrons result in a dipole structure with the oxygen end of the molecule negatively charged and the hydrogen end of the molecule positively charged. 3 The Water Molecule Dipole structure of water molecule produces an electrostatic bond (hydrogen bond) between water molecules. Hydrogen bonds form when the positive end of one water molecule bonds to the negative end of another water molecule. 4 2 Figure 4.1 5 The Dissolving Power of Water As solid sodium chloride dissolves, the positive and negative ions are attracted to the positive and negative ends of the polar water molecules. 6 3 Formation of Hydrated Ions Water dissolves salts by surrounding the atoms in the salt crystal and neutralizing the ionic bond holding the atoms together. 7 Important Property of Water: Heat Capacity Amount of heat to raise T of 1 g by 1oC Water has high heat capacity - 1 calorie Rocks and minerals have low HC ~ 0.2 cal. -
The Adsorption Characteristics of Cu(II)
www.nature.com/scientificreports OPEN The adsorption characteristics of Cu(II) and Zn(II) on the sediments at the mouth of a typical urban polluted river in Dianchi Lake: taking Xinhe as an example Xiang‑shu Ma1,2,3, Leng Liu1,2,3, Yi‑chuan Fang1,2,3 & Xiao‑long Sun1,2,3* This study is to determine the spatial distribution characteristics of Cu and Zn adsorption on the sediments of the estuary of Dianchi Lake, as well as the composite adsorption law of Cu and Zn on combinations of sediment organic matter, metal oxides, and organic–inorganic composites. The relationship between the adsorption contribution of each component of the substance. A static adsorption experiment was applied to the sediments in the estuary of Dianchi Lake. The relationship between adsorption capacity and sediment composition was analyzed through correlation analysis and redundant analysis. The results show that along the direction of the river fow and the vertical depth, the adsorption capacity presents a relatively obvious spatial distribution law; the change trend of sediment component content is not the same as the change trend of Cu and Zn adsorption capacity. The change trend of the sediment component content is not the same as the change trend of the adsorption amount of Cu and Zn, and the compound efect between the components afects the adsorption amount. The adsorption of Cu by the four groups of sediments after diferent treatments is more in line with the Freundlich isotherm adsorption model; When adsorbing Zn, the untreated and removed organic matter and iron‑aluminum oxide group are in good agreement with the Freundlich model, while the organic matter‑removed group and the iron‑aluminum oxide removal group are more consistent with the Langmuir isotherm adsorption model; The adsorption contribution rate of organic–inorganic composites in sediments is not a simple addition of organic matter and iron‑ aluminum oxides, but a more complex quantitative relationship. -
Thermophysical Properties of Materials for Water Cooled Reactors
XA9744411 IAEA-TECDOC-949 Thermophysical properties of materials for water cooled reactors June 1997 ¥DL 2 8 fe 2 Q The IAEA does not normally maintain stocks of reports in this series. However, microfiche copies of these reports can be obtained from IN IS Clearinghouse International Atomic Energy Agency Wagramerstrasse 5 P.O. Box 100 A-1400 Vienna, Austria Orders should be accompanied by prepayment of Austrian Schillings 100,- in the form of a cheque or in the form of IAEA microfiche service coupons which may be ordered separately from the IN IS Clearinghouse. IAEA-TECDOC-949 Thermophysical properties of materials for water cooled reactors WJ INTERNATIONAL ATOMIC ENERGY AGENCY /A\ June 1997 The originating Section of this publication in the IAEA was: Nuclear Power Technology Development Section International Atomic Energy Agency Wagramerstrasse 5 P.O. Box 100 A-1400 Vienna, Austria THERMOPHYSICAL PROPERTIES OF MATERIALS FOR WATER COOLED REACTORS IAEA, VIENNA, 1997 IAEA-TECDOC-949 ISSN 1011-4289 ©IAEA, 1997 Printed by the IAEA in Austria June 1997 FOREWORD The IAEA Co-ordinated Research Programme (CRP) to establish a thermophysical properties data base for light and heavy water reactor materials was organized within the framework of the IAEA's International Working Group on Advanced Technologies for Water Cooled Reactors. The work within the CRP started in 1990. The objective of the CRP was to collect and systematize a thenmophysical properties data base for light and heavy water reactor materials under normal operating, transient and accident conditions. The important thermophysical properties include thermal conductivity, thermal diffusivity, specific heat capacity, enthalpy, thermal expansion and others. -
Thickness and Structure of Adsorbed Water Layer and Effects on Adhesion and Friction at Nanoasperity Contact
colloids and interfaces Review Thickness and Structure of Adsorbed Water Layer and Effects on Adhesion and Friction at Nanoasperity Contact Chen Xiao 1, Pengfei Shi 1, Wenmeng Yan 1, Lei Chen 1,*, Linmao Qian 1 and Seong H. Kim 1,2 1 Tribology Research Institute, Key Laboratory of Advanced Technology of Materials, Ministry of Education, Southwest Jiaotong University, Chengdu 610031, China 2 Department of Chemical Engineering and Materials Research Institute, The Pennsylvania State University, University Park, PA 16802, USA * Correspondence: [email protected]; Tel.: +86-159-8213-9010 Received: 30 June 2019; Accepted: 2 August 2019; Published: 6 August 2019 Abstract: Most inorganic material surfaces exposed to ambient air can adsorb water, and hydrogen bonding interactions among adsorbed water molecules vary depending on, not only intrinsic properties of material surfaces, but also extrinsic working conditions. When dimensions of solid objects shrink to micro- and nano-scales, the ratio of surface area to volume increases greatly and the contribution of water condensation on interfacial forces, such as adhesion (Fa) and friction (Ft), becomes significant. This paper reviews the structural evolution of the adsorbed water layer on solid surfaces and its effect on Fa and Ft at nanoasperity contact for sphere-on-flat geometry. The details of the underlying mechanisms governing water adsorption behaviors vary depending on the atomic structure of the substrate, surface hydrophilicity and atmospheric conditions. The solid surfaces reviewed in this paper include metal/metallic oxides, silicon/silicon oxides, fluorides, and two-dimensional materials. The mechanism by which water condensation influences Fa is discussed based on the competition among capillary force, van der Waals force and the rupture force of solid-like water bridge.