Synthesis of a Dendrimer as Rheological Modifier for Deep-Water Drilling Fluids and Study of its Interaction with Organo-Clay at Different Temperatures

2018 ◽  
Vol 792 ◽  
pp. 111-118
Author(s):  
He Shi ◽  
Guan Cheng Jiang ◽  
Kai Wang ◽  
Xin Liang Li
Keyword(s):  
Deep Water ◽  
Optical Microscope ◽  
Large Temperature ◽  
Drilling Fluids ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Different Temperatures ◽  
Organo Clay ◽  
Rheological Test ◽  
Rheological Modifier

As the influence of large temperature range during deep-water drilling on rheological properties of water-in-oil emulsified drilling fluids, a dendrimer synthesized from a dodecyl dibasic acid and triethylenetetramine was introduced as a rheological modifier to get a flat-rheology. The product was characterized by infrared spectroscopy and its interaction with organo-clay was studied with sedimentation experiment, optical microscope, X-ray diffraction (XRD), Transmission electron microscopy (TEM), and rheological test. The results showed that the dendrimer can improve the dispersion of organo-clay in oil and increase the distance between layers. What’s more, the addition of dendrimer can balance the yield point of base slurry (consisted of mineral oil, aqueous solution of 30wt% CaCl2, mixed emulsifier, and organo-clay) at 4 ° C and 65 ° C.

Organoclay-reinforced polyethersulfone-modified epoxy-based hybrid nanocomposites

2011 ◽  
Vol 23 (7) ◽  
pp. 526-534 ◽  
Author(s):  
Yang Wang ◽  
Boming Zhang ◽  
Jinrui Ye
Keyword(s):  
Electron Microscopy ◽  
Fracture Toughness ◽  
Electron Microscope ◽  
Optical Microscope ◽  
Mechanical Analysis ◽  
Hybrid Nanocomposites ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Modified Epoxy ◽  
Scanning Electron

Hybrid nanocomposites were successfully prepared by the incorporation of polyethersulfone (PES) and organoclay into epoxy resin. They had higher fracture toughness than the prepared PES/epoxy blend and organoclay/epoxy nanocomposites. The microstructures of the hybrid nanocomposites were studied. They were comprised of homogeneous PES/epoxy semi-interpenetrating network (semi-IPN) matrices and organoclay micro-agglomerates made up of tactoid-like regions composed of ordered exfoliated organoclay with various orientations. The former was confirmed with dynamic mechanical analysis, scanning electron microscopy and transmission electron microscopy, while the latter was successfully observed with X-ray diffraction measurements, optical microscope, scanning electron microscope and transmission electron microscope. The improvement of their fracture toughness was due to the synergistic toughening effect of the PES and the organoclay and related to their microstructures.

scholarly journals Effect of Annealing on the ZnS Nanocrystals Prepared by Chemical Precipitation Method

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Nadana Shanmugam ◽  
Shanmugam Cholan ◽  
Natesan Kannadasan ◽  
Kannadasan Sathishkumar ◽  
G. Viruthagiri
Keyword(s):  
Chemical Precipitation ◽  
Chemical Precipitation Method ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Visible Absorption ◽  
Atomic Force ◽  
Transmission Electron ◽  
Different Temperatures ◽  
Uv Visible ◽  
Dta Curves

Nanocrystals of ZnS have been synthesized through simple chemical precipitation method using thiourea as sulphur source. The synthesized products were annealed at different temperatures in the range of 200–800∘C. The as-synthesized and annealed samples were characterized by X-ray diffraction (XRD), UV-Visible absorption (UV-Vis), and room temperature photoluminescence (PL) measurements. The morphological features of ZnS annealed at 200 and 500∘C were studied by atomic force microscope (AFM) and transmission electron microscope (TEM) techniques. The phase transformation of ZnS and formation of ZnO were confirmed by thermogravimetric (TG) and differential thermal analysis (DTA) curves.

Fe–Cr/Al2O3 metal-ceramic composites: Nature and size of the metal particles formed during hydrogen reduction

1994 ◽  
Vol 9 (1) ◽  
pp. 229-235 ◽  
Author(s):  
Ch. Laurent ◽  
J.J. Demai ◽  
A. Rousset ◽  
K.R. Kannan ◽  
C.N.R. Rao
Keyword(s):  
Hydrogen Reduction ◽  
Ceramic Composites ◽  
X Ray Diffraction ◽  
X Ray ◽  
Total Reduction ◽  
Transmission Electron ◽  
Combined Use ◽  
Metal Ceramic ◽  
Different Temperatures ◽  
Metallic Species

Fe-Cr/Al2O3 metal-ceramic composites prepared by hydrogen reduction at different temperatures and for different periods have been investigated by a combined use of Mössbauer spectroscopy, x-ray diffraction, transmission electron microscopy, and energy-dispersive x-ray spectroscopy in order to obtain information on the nature of the metallic species formed. Total reduction of Fe3+ does not occur by increasing the reduction time at 1320 K from 1 to 30 h, and the amount of superparamagnetic metallic species is essentially constant (about 10%). Temperatures higher than 1470 K are needed to achieve nearly total reduction of substitutional Fe3+. Interestingly, iron favors the reduction of chromium. The composition of the Fe-Cr particles is strongly dependent on their size, the Cr content being higher in particles smaller than 10 nm.

Preparation and Property of Al87Ce3Ni8.5Mn1.5 Nanophase Amorphous Composites

2011 ◽  
Vol 412 ◽  
pp. 263-266
Author(s):  
Hong Wei Zhang ◽  
Li Li Zhang ◽  
Feng Rui Zhai ◽  
Jia Jin Tian ◽  
Can Bang Zhang
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Single Phase ◽  
Volume Fraction ◽  
Material Structure ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
Different Temperatures

The higher mechanical strength of Al87Ce3Ni8.5Mn1.5 nanophase amorphous composites has been obtained with two methods. The first nanophase amorphous composites are directly produced by the single roller spin quenching technology. The method taken for the second nanophase amorphous composites is at first to obtain amorphous single-phase alloy, followed by annealed at different temperatures .The formative condition, the microstructure, the particle size, the volume fraction of α-Al phase and microhardness of nanophase amorphous composites etc have been investigated and compared by X-ray diffraction (XRD) and transmission electron microscopy (TEM) and differential scanning calorimetry (DSC). The microstructure of composites produced by the second method is higher than the former, the fabricated material structure of the system is more uniform and the process is easier to control.

The Features of a High-Temperature Synthesis of ZrO2 in a Core-Shell ZrO2@C Structure

2019 ◽  
Vol 950 ◽  
pp. 133-137
Author(s):  
Alexander M. Volodin ◽  
Vladimir O. Stoyanovskii ◽  
Vladimir I. Zaykovskii ◽  
Roman M. Kenzhin ◽  
Aleksey A. Vedyagin
Keyword(s):  
Elevated Temperatures ◽  
Cubic Phase ◽  
Core Shell ◽  
X Ray Diffraction ◽  
High Temperature Synthesis ◽  
Transmission Electron ◽  
Different Temperatures ◽  
Carbon Coated ◽  
Physicochemical Methods ◽  
Argon Adsorption

Zirconium oxide was obtained via traditional precipitation from a ZrOCl2 solution with ammonia followed by drying at 110 °C. The carbon-coated samples were synthesized by calcination of the pristine zirconia mixed with polyvinylalcohol. The obtained ZrO2@C samples of core-shell structure as well as the reference samples of pristine zirconia were calcined at different temperatures from 500 to 1400 °C. All the materials were examined by a set of physicochemical methods (a low-temperature argon adsorption, transmission electron microscopy, X-ray diffraction analysis, photoluminescence spectroscopy). It was found that the carbon coating prevents the sintering of the oxide nanoparticles, which allows one to maintain the specific surface area, the size of the oxide core and, finally, stabilize its phase composition. Transformation of the cubic phase into monoclinic phase becomes significantly complicated. Thus, 40% of the cubic phase was detected even after calcination of the ZrO2@C sample at 1400 °C. Moreover, the carbon-coated samples treated at elevated temperatures with subsequent removal of the carbon shell were found to possess the highest concentration of the defects related to a presence of the anion vacancies in zirconia.

Synthesis and Activity of Co-doped Barium Cerium Zirconate for Hydrogen Reforming and Purification

2008 ◽  
Vol 1126 ◽  
Author(s):  
Aravind Suresh ◽  
Joysurya Basu ◽  
Nigel M Sammes ◽  
Barry C Carter ◽  
Benjamin A Wilhite
Keyword(s):  
Hydrogen Generation ◽  
Ac Impedance ◽  
Cubic Phase ◽  
X Ray Diffraction ◽  
Ac Impedance Spectroscopy ◽  
Methanol Partial Oxidation ◽  
Transmission Electron ◽  
Catalytically Active ◽  
Different Temperatures ◽  
Co Precipitation

AbstractBaCe0.25Zr0.60Co0.15O3-x (BCZC) was synthesized via oxalate co-precipitation route. Material was characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Catalytic activity of BCZC with respect to hydrogen generation via methanol partial oxidation was determined. Conductivity of the material at different temperatures and under different environments was determined by AC impedance spectroscopy. XRD and TEM results indicated that BCZC was synthesized as a homogeneous cubic phase material. Catalyst tests indicated that BCZC was catalytically active towards hydrogen generation and AC impedance results were positive enough to warrant further electrochemical studies.

Effect of Calcination Temperature on the Morphological and Phase Structure of Hydrothermally Synthesized Copper Ion Doped TiO2 Nanotubes

2014 ◽  
Vol 1024 ◽  
pp. 7-10 ◽  
Author(s):  
Mohd Hasmizam Razali ◽  
M.N. Ahmad-Fauzi ◽  
Abdul Rahman Mohamed ◽  
Srimala Sreekantan
Keyword(s):  
Calcination Temperature ◽  
Morphological Evolution ◽  
Copper Ion ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Different Temperatures ◽  
Scanning Electronmicroscopy ◽  
Higher Temperature ◽  
Uniform Diameter

Morphological evolution and phase transformations of copper ion doped TiO2nanotubes after being calcined at different temperatures were studied by field emission scanning electronmicroscopy, transmission electron microscopy, and X-ray diffraction. After calcination at 300°C, the nanotubes with uniform diameter and length wereobtained. At 400°C, the nanotube structures were maintained. Nevertheless the inner tube diameter became narrower, and in same instances disappeared due to aggregation of nanotubes. The copper ion doped TiO2nanotubes then transformed to nanorodsat 500°C and the length of the nanorodsshortens after calcination at 600 °C. When the calcination temperature was further increased to 700°C, the nanorodsdisintegrate to form nanoparticles. On the other hand the phase structures of copper ion doped TiO2nanotubes calcined at 300 and 400 °C were TiO2hexagonal. After calcined at higher temperature (600 and 700°C) they transformed to anatase TiO2(tetragonal).

scholarly journals Effect of Reaction Temperature on Size and Optical Properties of NiTiO3Nanoparticles

2012 ◽  
Vol 9 (1) ◽  
pp. 282-288 ◽  
Author(s):  
R. Vijayalakshmi ◽  
V. Rajendran
Keyword(s):  
Electron Microscopy ◽  
Particle Size ◽  
Uv Spectroscopy ◽  
Particle Size Effect ◽  
Infrared Spectrometry ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Nickel Titanate ◽  
Different Temperatures ◽  
Wet Chemical

Nickel titanate (NiTiO3) nanoparticles were successfully prepared by wet-chemical method, using nickel acetate and titanium(IV) isopropoxide as Ni, Ti sources and citric acid as complexing reagent. The gel was calcined at different temperatures from 500-700 °C. Results of thermogravimetric analysis (TGA) are given. Fourier transform infrared spectrometry (FTIR), X-ray diffraction (XRD), Scanning electron microscopy (SEM),transmission electron microscopy (TEM), ultraviolet (UV) spectroscopy, vibrating sample magnetometer (VSM) were used to characterize the crystallization process, particle size, morphology, optical and magnetic properties of the calcined nanoparticles. TEM result reveals that the NiTiO3was homogeneous and hexagon morphology with the grain size of 30-70 nm. The band gap values of the NiTiO3nanoparticles were calculated to be 3.43, 3.39 and 3.31 eV. The magnetic property was confirmed that the NiTiO3nanoparticles of super paramagnetic behavior in nature. Our results suggested that the temperature plays an important role in the particle size effect of nanocrystalline NiTiO3.

A new high-temperature inorganic–organic proton conductor: lanthanum sulfophenyl phosphate

2016 ◽  
Vol 70 (3) ◽  
Author(s):  
Ming-Feng Song ◽  
Zhong-Fang Li ◽  
Guo-Hong Liu ◽  
Su-Wen Wang ◽  
Xiao-Yan Yin ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Layered Structure ◽  
Proton Conductor ◽  
X Ray Diffraction ◽  
X Ray ◽  
Good Thermal Stability ◽  
Transmission Electron ◽  
Good Crystallinity ◽  
Different Temperatures ◽  
Thermal Stability Of

AbstractLanthanum sulfophenyl phosphate (LaSPP) was synthesized by m-sulfophenyl phosphonic acid and lanthanum nitrate. UV-Vis spectrophotometry and Fourier-transform infrared spectroscopy indicate that the desired product was obtained and its elementary composition and typical layered structure were determined by energy dispersive X-ray spectroscopy and scanning electron microscopy. Transmission electron microscopy (TEM) proved its typical layered structure and X-ray diffraction spectroscopy indicated its good crystallinity and the interlayer distance of about 15.67 Å , which matches the value obtained by TEM (2.0 nm). Thermogravimetry and differential thermal analysis revealed good thermal stability of LaSPP. Proton conductivity of LaSPP was measured at different temperatures and relative humidities (RH), reaching values of 0.123 S cm

Microstructure and Creep Behaviors of As-Cast Mg-Zn-Er Alloys

2017 ◽  
Vol 898 ◽  
pp. 305-310
Author(s):  
Rui Jing Li ◽  
Shu Bo Li ◽  
Ke Liu ◽  
Zhao Hui Wang ◽  
Xian Du ◽  
...  
Keyword(s):  
Electron Microscope ◽  
Creep Strain ◽  
Volume Fraction ◽  
Cast Alloy ◽  
Optical Microscope ◽  
Quasicrystalline Phase ◽  
X Ray Diffraction ◽  
Creep Tests ◽  
Transmission Electron ◽  
Icosahedral Quasicrystalline

The microstructure and creep behaviors of cast Mg-xZn-yEr (x=3,6,9 wt.%, x/y=6) alloys were investigated by X-ray diffraction (XRD), optical microscope (OM), scanning electron microscope (SEM) and transmission electron microscope (TEM). XRD results indicated that the main phase compositions of as-cast Mg-xZn-yEr alloys were the icosahedral quasicrystalline phase (I-phase) and α-Mg solid solution. The I-phase mainly distributed in the dendritic and staccato strips. The creep tests were conducted under the condition of 448 K, 70 MPa for 100 h. As the addition of Er increased from 0.5 wt.% to 1.5 wt.%, the total creep strain decreased from 0.962% to 0.512%, and the steady state creep rate decreased from 1.411×10-8s-1 to 4.917×10-9s-1. The I-phase had a tendency to be bulky and continuous, as the volume fraction of Er element increased. Ascribed to the I-phase, the creep strain happened and effectively blocked the movement of dislocations, resulting in the strengthened as-cast Mg-Zn-Er alloys and improved creep resistance. Based on the investigation of creep behaviors, the creep mechanism of the as-cast alloy was mainly grain boundary slipping.

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