Effects of montmorillonite nanoclay on the properties of chemimechanical pulping paper

BioResources ◽  
2021 ◽  
Vol 16 (3) ◽  
pp. 6281-6291
Author(s):  
Jafar Ebrahimpour Kasmani ◽  
Ahmad Samariha
Keyword(s):  
Tensile Strength ◽  
Morphological Properties ◽  
X Ray Diffraction ◽  
Cationic Starch ◽  
Burst Strength ◽  
X Ray ◽  
Air Resistance ◽  
Diffraction Patterns ◽  
Montmorillonite Nanoclay ◽  
Scanning Electron

The effects of nanoclay were studied relative to the physical, mechanical, optical, and morphological properties of chemimechanical pulping papers. Nanoclay was incorporated at 0%, 2%, 4%, 6%, 8%, or 10%. To increase the retention, 1% cationic starch was used in all test papers. Handsheets (60 g/m2 in weight) were tested to determine their physical, mechanical, optical, and morphological properties. Up to 2% nanoclay increased the tensile strength; at values greater than 2%, the tensile strength decreased. The addition of up to 4% nanoclay increased roughness; between 4% and 10% nanoclay, roughness decreased. With 10% nanoclay, the tear strength, burst strength, and brightness decreased, but the air resistance, opacity, and yellowness increased. Scanning electron microscopy showed that the nanoclay filled the pore spaces between fibers, thus increasing air resistance. X-ray diffraction patterns indicated an intercalated structure.

Compositional, Structural and Morphological Analyses of Bulk GeS Alloy and its Thin Films

2021 ◽  
Vol 1039 ◽  
pp. 398-405
Author(s):  
Munira M.J. Al-Haji ◽  
Raad M.S. Al-Haddad
Keyword(s):  
Electron Microscopy ◽  
Thin Films ◽  
Thermal Evaporation ◽  
Source Material ◽  
Morphological Properties ◽  
X Ray Diffraction ◽  
Melt Quenching ◽  
X Ray ◽  
Vacuum Thermal Evaporation ◽  
Scanning Electron

Bulk Germanium monosulphide (GeS) alloy was synthesized using the usual melt-quenching technique. Its grains were used as the source material to deposit thin films by vacuum thermal evaporation. Thin-films samples were doped with 1, 2, and 3 at.% indium by thermal co-evaporation and annealed in a vacuum at temperatures 373, 473 and 550 K for an hour. Compositional, structural, and morphological properties of the bulk GeS alloy and its thin films were investigated by Energy Dispersive X-Ray Spectroscopy (EDS), X-Ray Diffraction (XRD), and Scanning Electron Microscopy (SEM) techniques. The analyses verified the stoichiometry (GeS) of the starting material in the prepared thin films. They also revealed that the thin films under study are amorphous, homogeneous, without any cracks deposited uniformly on the glass substrate with thickness 650 to 700 nm.

Structure and properties of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate)/poly(L-lactic acid) quasi core/sheath melt-electrospun microfibers

2018 ◽  
Vol 89 (9) ◽  
pp. 1770-1781 ◽  
Author(s):  
Huaizhong Xu ◽  
Benedict Bauer ◽  
Masaki Yamamoto ◽  
Hideki Yamane
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Lactic Acid ◽  
Tensile Tests ◽  
Processing Parameters ◽  
Structure And Properties ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Diffraction Patterns

A facile route was proposed to fabricate core–sheath microfibers, and the relationships among processing parameters, crystalline structures and the mechanical properties were investigated. The compression molded poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBH)/poly(L-lactic acid) (PLLA) strip enhanced the spinnability of PHBH and the mechanical properties of PLLA as well. The core–sheath ratio of the fibers was determined by the prefab strip, while the PLLA sheath component did not completely cover the PHBH core component due to the weak interfacial tension between the melts of PHBH and PLLA. A rotational target was applied to collect aligned fibers, which were further drawn in a water bath. The tensile strength and the modulus of as-spun and drawn fibers increased with increasing the take-up velocities. When the take-up velocity was above 500 m/min, the jet became unstable and started to break up at the tip of the Taylor cone, decreasing the mechanical properties of the fibers. The drawing process facilitated the crystallization of PLLA and PHBH, and the tensile strength and the modulus increased linearly with the increasing the draw ratio. The crystal information displayed from wide-angle X-ray diffraction patterns and differential scanning calorimetry heating curves supported the results of the tensile tests.

Sintering AlN Ceramics Below 1500°C with MgO-CaO-Al2O3-SiO2 Glass Addition

2007 ◽  
Vol 336-338 ◽  
pp. 1868-1871 ◽  
Author(s):  
Cheng Fu Yang ◽  
Chien Min Cheng ◽  
Ho Hua Chung ◽  
Chao Chin Chan
Keyword(s):  
Sintering Temperature ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Dielectric Characteristics ◽  
Sintering Aid ◽  
Glass Addition ◽  
X Ray ◽  
Crystal Phases ◽  
Diffraction Patterns ◽  
Scanning Electron

5~15 wt% MgO-CaO-Al2O3-SiO2 (MCAS, fabricated by sol-gel method) glass is used as the sintering aid of AlN ceramics. The sintering is proceeded from 1350oC~1550oC, scanning electron microscope is used to observe the sintered morphologies and X-ray diffraction pattern are used to confirm the crystal structures. From the SEM observations, as 10wt% and 15wt% MCAS is added, AlN ceramics can be densified at 1500oC and 1450oC, which are much lower than the before studies were. From the X-ray diffraction patterns, the crystal phases of MCAS-AlN ceramics are AlN, Al2O3, and cordierite phases. In this study, the dielectric characteristics of MCAS-AlN ceramics are also developed as a function of MCAS content and sintering temperature.

Effect of FLiBe Infiltration Pressure on Microstructure of Matrix for TMSR Fuel Elements (FEs)

2017 ◽  
Vol 373 ◽  
pp. 189-192
Author(s):  
Hong Xia Xu ◽  
Jun Lin ◽  
Yu Chen ◽  
Bing Chuan Gu ◽  
Bang Jiao Ye ◽  
...  
Keyword(s):  
Positron Lifetime ◽  
X Ray Diffraction ◽  
X Ray ◽  
Positron Annihilation Lifetime ◽  
Infiltration Pressure ◽  
Matrix Graphite ◽  
The Matrix ◽  
Diffraction Patterns ◽  
Fuel Elements ◽  
Scanning Electron

The matrix graphite of fuel elements (FEs) with infiltration of 2LiF-BeF2(FLiBe) at different pressures varying from 0.4 MPa to 1.0 MPa, has been studied by X-ray diffraction (XRD), scanning electron microscope (SEM) and positron annihilation lifetime (PAL) measurement. The result of XRD reveals that diffraction patterns of FLiBe appear in matrix graphite infiltrated with FLiBe at a pressure of 0.8 MPa and 1.0 MPa. The surface morphology from SEM shows that FLiBe mainly distributes within macro-pores of matrix graphite. PAL measurement indicates that there are mainly two positron lifetime components in all specimens:τ1~0.21 ns and τ2 ­~0.47 ns, ascribed to annihilation of positrons in bulk and trapped-positrons at surface, respectively. The average positron lifetime decreases with infiltration pressure, due to the decrease in annihilation fraction of positrons with surface after infiltration of FLiBe into macro-pores.

Study on Microstructure and Property of Diffusion-Bonded Mo-Cu Joints

2012 ◽  
Vol 508 ◽  
pp. 178-182
Author(s):  
Jian Zhang ◽  
Guo Qiang Luo ◽  
Mei Juan Li ◽  
Qiang Shen ◽  
Lian Meng Zhang
Keyword(s):  
Electron Microscopy ◽  
Mechanical Property ◽  
Tensile Strength ◽  
Electron Probe ◽  
Bonding Process ◽  
Interfacial Structure ◽  
X Ray Diffraction ◽  
Strength Measurement ◽  
X Ray ◽  
Scanning Electron

Mo and Cu Were Bonded Successfully by Means of Vacuum Diffusion Bonding. The Interfacial Structure of the Joints Was Studied by Scanning Electron Microscopy (SEM), Electron Probe Microanalysis (EPMA), Energy Dispersive X-Ray Spectrometer (EDS) and X-Ray Diffraction (XRD), the Mechanical Property Is Tested by Tensile Strength Measurement. The Results Showed that the Differentatoms Diffused to each other in the Bonding Process. A Mo-Cu Solid Solution Was Formed in the Joint and with No Intermetallic Compounds. The Tensile Strength of the Joint Increased with the Increasing of Temperature, however, while the Holding Time Increased, the Strength Increased in the First Stages and then Decreases. It Were Observed that the Fracture Mode of the Joints Was a Brittle Fracture.

Effect of the Dwell Temperature on Spark Plasma Sintered CaCu3Ti4O12

2012 ◽  
Vol 727-728 ◽  
pp. 982-987
Author(s):  
E. de Carvalho ◽  
Marcelo Bertolete ◽  
Izabel Fernanda Machado ◽  
E.N.S. Muccillo
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Lattice Parameter ◽  
Solid State Reactions ◽  
X Ray Diffraction ◽  
X Ray ◽  
Plasma Sintering ◽  
Spark Plasma ◽  
Diffraction Patterns ◽  
Scanning Electron

Polycrystalline CaCu3Ti4O12 ceramics were prepared by solid state reactions by spark plasma sintering (SPS) technique. In this study, the effects of the dwell temperature on structural, microstructural and dielectric properties of CaCu3Ti4O12 ceramics have been investigated. Powder mixtures were calcined at 900°C for 18 h before SPS consolidation. The dwell temperatures were 850, 900, 915 and 930°C. Sintered pellets were characterized by X-ray diffraction, scanning electron microscopy and impedance spectroscopy. X-ray diffraction patterns show evidences of a single-phase perovskite-type structure. The calculated lattice parameter is 7.40 Å. The hydrostatic density increases slightly with increasing dwell temperature. Scanning electron microscopy observations revealed a heterogeneous microstructure for all samples. The dielectric loss remains constant over a wide temperature range. The obtained permittivity is approximately 103 at 1 kHz. The increase of the dwell temperature is found to produce a brittle ceramic.

Structural and Morphological Properties of HfxZr1-xO2 Thin Films Prepared by Pechini Route

2010 ◽  
Vol 644 ◽  
pp. 113-116
Author(s):  
L.A. García-Cerda ◽  
Bertha A. Puente Urbina ◽  
M.A. Quevedo-López ◽  
B.E. Gnade ◽  
Leo A. Baldenegro-Perez ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thin Films ◽  
Annealing Temperature ◽  
Precursor Solution ◽  
Dip Coating ◽  
Morphological Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dip Coating Technique ◽  
Scanning Electron

In this study, HfxZr1-xO2 (0 < x < 1) thin films were deposited on silicon wafers using a dip-coating technique and by using a precursor solution prepared by the Pechini route. The effects of annealing temperature on the structure and morphological properties of the proposed films were investigated. HfxZr1-xO2 thin films with 1, 3 and 5 layers were annealed in air for 2 h at 600 and 800 °C and the structural and morphological properties studied by X-ray diffraction (XRD) and scanning electron microscopy (SEM). XRD results show that the films have monoclinic and tetragonal structure depending of the Hf and Zr concentration. SEM photographs show that all films consist of nanocrystalline grains with sizes in the range of 6 - 13 nm. The total film thickness is about 90 nm.

Effect of friction time on tensile strength and metallurgical properties of friction welded dissimilar aluminum alloy joints

2021 ◽  
Vol 63 (12) ◽  
pp. 1097-1103
Author(s):  
M. Bakkiyaraj ◽  
A. K. Lakshminarayanan ◽  
S. Yuvaraj ◽  
P. K. Nagarajan
Keyword(s):  
Electron Microscopy ◽  
Tensile Strength ◽  
Dissimilar Metals ◽  
X Ray Diffraction ◽  
X Ray ◽  
Rotating Speed ◽  
Metallurgical Properties ◽  
Metallurgical Bonding ◽  
Friction Pressure ◽  
Scanning Electron

Abstract Dissimilar (AA6061 & AA7075-T6) friction welded aluminum joints were taken into the investigation to correlate the influences of friction time on tensile and metallurgical properties. The dissimilar metals were welded by varying the friction time from 2 s to 6 s with the following constant parameters: a rotating speed of 1200 rpm, friction pressure of 35 MPa, upset pressure of 35 MPa, and upset time of 3 s. The higher friction time during joint fabrication needs to be selected to attain good metallurgical bonding between rubbing surfaces. The highest tensile strength of 228 MPa was attained when the friction time was given as 4 s. Furthermore, the increase in friction time widened the width and reduced the hardness of the heat affected zone on the AA6061 side where joint failure occurred. Finally, the metallurgical features of the dissimilar specimens were characterized using optical microscopy, scanning electron microscopy, and X-ray diffraction. Other details related to the characterization and results of the testing were recounted.

Synthesis of Ni-Mo-W Sulfide Nanorods as Catalyst for Hydrodesulfurization of Dibenzothiophene

2008 ◽  
Vol 8 (12) ◽  
pp. 6406-6413 ◽  
Author(s):  
F. Paraguay-Delgado ◽  
R. García-Alamilla ◽  
J. A. Lumbreras ◽  
E. Cizniega ◽  
G. Alonso-Núñez
Keyword(s):  
Electron Microscopy ◽  
Physical Adsorption ◽  
Atomic Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Oxide Precursor ◽  
Transmission Electron ◽  
Adsorption Of Nitrogen ◽  
Diffraction Patterns ◽  
Scanning Electron

Two trimetallic sulfurs, MoWNiS and MoWSNi, were synthesized to be used as a catalyst in hydrodesulfurization reactions. The mixed oxide mesoporous nanostructured MoO3-WO3 with an Mo:W atomic ratio of 1:1 was used as the precursor. The first catalyst was prepared by impregnating nickel in the oxide precursor and then subsequent sulfiding with an H2S/H2 mix at 400 °C for 2 hours. The second catalyst was prepared by sulfiding the precursor and then impregnating the nickel, and finally reducing the material with a H2/N2 at 350 °C. In both catalysts the Mo:W:Ni atomic ratio was maintained at 1:1:0.5. The materials obtained were characterized by physical adsorption of nitrogen, X-ray diffraction, scanning electron microscopy, transmission electron microscopy. Furthermore, the materials obtained were evaluated by a dibenzothiophene hydrodesulfuration reaction. The diffraction patterns show that both materials are polycrystalline and mainly of MoS2 and WS2 phases.

scholarly journals Preparation and Characterization of High Purity Anhydrous β-Lactose from α-Lactose Monohydrate at Mild Temperature

2018 ◽  
Vol 2018 ◽  
pp. 1-10 ◽  
Author(s):  
Ana L. López-Pablos ◽  
César C. Leyva-Porras ◽  
Macrina B. Silva-Cázares ◽  
Francisco E. Longoria-Rodríguez ◽  
Sergio A. Pérez-García ◽  
...  
Keyword(s):  
Room Temperature ◽  
Alcoholic Solution ◽  
X Ray Diffraction ◽  
X Ray ◽  
Lactose Monohydrate ◽  
Diffraction Patterns ◽  
Mild Temperature ◽  
Dietary Food ◽  
Scanning Electron

Lactose is a disaccharide of importance in humans dietary, food products, and the pharmaceutical industry. From the existing isomeric forms, β-lactose is rarely found in nature. Thus, in this work, a simple methodology to obtain anhydrous β-lactose (βL) from α-lactose monohydrate (αL·H2O) is presented. The αL·H2O powder was dispersed into a basic alcoholic solution (72 hours), at controlled conditions of temperature (27, 29, 31, and 32°C), without stirring. The slurry was dried at room temperature and characterized. Fourier transform infrared spectroscopy showed the formation of βL for the samples prepared at 29 and 32°C. Raman spectroscopy confirmed this result and suggested the occurrence of crystalline βL. Rietveld refinement of the X-ray diffraction patterns was employed to identify and quantify the composition of the isomers. The samples prepared at 29 and 31°C showed the formation of pure βL, while those at 27 and 32°C showed the presence of αL·H2O and a mixture of the two isomers, respectively. The morphology of the powders was studied by scanning electron microscopy, observing the formation of irregular shape αL·H2O particles and axe-like βL particles. Clearly, with this methodology, it was possible to obtain pure, crystalline, and anhydrous βL at mild temperature.

Sign in / Sign up

Export Citation Format

Share Document