scholarly journals Membranes for Cation Transport Based on Dendronized Poly(epichlorohydrin-co-ethylene oxide). Part 1: The Effect of Dendron Amount and Column Orientation on Copolymer Mobility

Polymers ◽  
2021 ◽  
Vol 13 (20) ◽  
pp. 3532
Author(s):  
Alireza Zare ◽  
Borja Pascual-Jose ◽  
Silvia De la De la Flor ◽  
Amparo Ribes-Greus ◽  
Xavier Montané ◽  
...  
Keyword(s):  
Thermal Analysis ◽  
Ethylene Oxide ◽  
Annealing Treatment ◽  
Cation Transport ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Dielectric Thermal Analysis ◽  
Thermal Annealing Treatment ◽  
Partial Crystallization ◽  
Oriented Membranes

Dendronized polyethers give rise to columnar LC structures which can successfully act as cation transport materials. Therefore, we prepared two different materials, based on Poly(epichlorohydrin-co-ethylene oxide) (PECH-co-EO) grafted with methyl 3,4,5-tris[4-(n-dodecan-1-yloxy)benzyloxy] benzoate, containing 20% or 40% modified units, respectively. The obtained polymers were characterized by differential scanning calorimetry (DSC), X-ray diffraction and optical microscopy between crossed polars (POM) and compared to the unmodified PECH-co-EO. In order to reach efficient transport properties, homeotropically oriented membranes were prepared by a fine-tuned thermal annealing treatment and were subsequently investigated by dynamic mechanical thermal analysis (DMTA) and dielectric thermal analysis (DETA). We found that the presence of the dendrons induces a main chain partial crystallization of the polyether chain and coherently increases the polymer Tg. This effect is more evident in the oriented membranes. As for copolymer orientation upon annealing, the cooling rate and the annealing temperature were the most crucial factors. DMTA and DETA confirmed that grafting with the dendron strongly hinders copolymer motions, but did not show great differences between unoriented and oriented membranes, regardless of the amount of dendrons.

Human cytokines characterized by dielectric thermal analysis, thermogravimetry, and differential scanning calorimetry

2012 ◽  
Vol 111 (3) ◽  
pp. 1707-1716 ◽  
Author(s):  
Salaam Saleh ◽  
Druthiman Reddy Mantheni ◽  
Manik Pavan Kumar Maheswaram ◽  
Susan Moreno-Molek ◽  
Tobili Sam-Yellowe ◽  
...  
Keyword(s):  
Thermal Analysis ◽  
Differential Scanning Calorimetry ◽  
Scanning Calorimetry ◽  
Dielectric Thermal Analysis ◽  
Human Cytokines

Improved Photovoltaic Efficiency of Polymer Photovoltaic Cells by Microwave Irradiation

2010 ◽  
Vol 663-665 ◽  
pp. 819-822
Author(s):  
Boeun Kim ◽  
Kyeong K. Lee ◽  
Sung Koo Lee ◽  
Eun Hee Lim
Keyword(s):  
Thermal Annealing ◽  
Acid Methyl Ester ◽  
Annealing Treatment ◽  
Polymer Chains ◽  
X Ray Diffraction ◽  
Force Microscopy ◽  
Microwave Annealing ◽  
Photovoltaic Efficiency ◽  
Atomic Force ◽  
Thermal Annealing Treatment

In this study, microwave annealing treatment was introduced into poly(3-hexylthiophene) (P3HT):[6,6]-phenyl-C61butyric acid methyl ester (PCBM) and poly(9,9‘-dioctylfluorene-cobithiophene (PFT2):PCBM systems instead of thermal annealing treatment. In both systems, microwave annealing showed photovoltaic performane comparable to that of conventional thermal annealing. Through the UV-vis absorption, atomic force microscopy (AFM) and X-ray diffraction (XRD) studies, we were able to confirm that the microwave annealing increases the crystallization of the P3HT polymer chains.

Synthesis, Characterization and Magnetism of Nanosized Copper Ferrite

2008 ◽  
Vol 368-372 ◽  
pp. 604-606 ◽  
Author(s):  
Wei Zhong Lv ◽  
Zhong Kuang Luo ◽  
Bo Liu ◽  
Xiang Zhong Ren ◽  
Hong Hua Cai ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Copper Ferrite ◽  
Sonochemical Method ◽  
Thermal Gravimetric ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Ft Ir ◽  
Scanning Electron

Copper ferrite powders were successfully synthesized by sonochemical method. The resultant powders were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), FT-IR, differential thermal analysis-thermal gravimetric (DTA-TG), differential scanning calorimetry (DSC) and VSM. The particle saturation magnetization (Ms) is 66 emu/g and an intrinsic coercive force (iHc) is 2100 Oe when the precursor calcined at 950 °C for 15 h.

scholarly journals The Usefulness of X-ray Diffraction and Thermal Analysis to Study Dietary Supplements Containing Iron

Molecules ◽  
2021 ◽  
Vol 27 (1) ◽  
pp. 197
Author(s):  
Izabela Jendrzejewska ◽  
Robert Musioł ◽  
Tomasz Goryczka ◽  
Ewa Pietrasik ◽  
Joanna Klimontko ◽  
...  
Keyword(s):  
Thermal Analysis ◽  
Melting Point ◽  
Dietary Supplements ◽  
Polymorphic Form ◽  
Food Supplements ◽  
X Ray Diffraction ◽  
Iron Compounds ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Amorphous Compounds

X-ray powder diffraction (XRPD) and thermal analysis (differential scanning calorimetry/derivative of thermogravimetry (DSC/DTG)) are solid-state techniques that can be successfully used to identify and quantify various chemical compounds in polycrystalline mixtures, such as dietary supplements or drugs. In this work, 31 dietary supplements available on the Polish market that contain iron compounds, namely iron gluconate, fumarate, bisglycinate, citrate and pyrophosphate, were evaluated. The aim of the work was to identify iron compounds declared by the manufacturer as food supplements and to try to verify compliance with the manufacturer’s claims. Studies performed by X-ray and thermal analysis confirmed that crystalline iron compounds (iron (II) gluconate, iron (II) fumarate), declared by the manufacturers, were present in the investigated dietary supplements. Iron (II) bisglycinate proved to be semi-crystalline. However, depending on the composition of the formulation, it was possible to identify this compound in the tested supplements. For amorphous iron compounds (iron (III) citrate and iron (III) pyrophosphate), the diffraction pattern does not have characteristic diffraction lines. Food supplements containing crystalline iron compounds have a melting point close to the melting point of pure iron compounds. The presence of excipients was found to affect the shapes and positions of the endothermic peaks significantly. Widening of endothermic peaks and changes in their position were observed, as well as exothermic peaks indicating crystallization of amorphous compounds. Weight loss was determined for all dietary supplements tested. Analysis of the DTG curves showed that the thermal decomposition of most food supplements takes place in several steps. The results obtained by a combination of both simple, relatively fast and reliable XRPD and DSC/DTG methods are helpful in determining phase composition, pharmaceutical abnormalities or by detecting the presence of the correct polymorphic form.

Effect of Annealing Treatment on the Microstructure and Magnetic Properties of FeSiBAlNi(C, Ce) High Entropy Alloys

2016 ◽  
Vol 849 ◽  
pp. 52-57 ◽  
Author(s):  
Jing Xu ◽  
Zheng Feng Zhao ◽  
Yan Wang
Keyword(s):  
Magnetic Properties ◽  
Amorphous Phase ◽  
Annealing Treatment ◽  
Particle Morphology ◽  
High Entropy Alloys ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
High Entropy ◽  
Temperature Range ◽  
Microstructure And Magnetic Properties

In this paper, the effects of annealing treatment on the microstructure, thermal property and magnetic properties of mechanical alloyed FeSiBAlNiC and FeSiBAlNiCe amorphous high entropy alloys has been systematically investigated using X-ray diffraction, differential scanning calorimetry, field emission scanning electron microscopy and alternation gradient magnetometry. The results showed that annealing at different temperature range induced the pronounced microstructural evolution from the amorphous phase to a mixture of amorphous phase and intermetallics but without any formation of solid solutions. In addition, the thermal stability and heat resistance were enhanced with increasing the annealing temperature. Similarly, annealing treatment also had significant effect on the particle morphology, making the particles evolve from near-round shape to plate-like shape. Furthermore, subsequent annealing of W6-Ce amorphous HEAs enhanced the saturation magnetization (Ms) remarkably (from 0.6 emu/g of 140 h as-milled W6-Ce to 20.17 emu/g). But for the Ms values of the 140 h as-milled amorphous W6-C HEAs, annealing in different temperature range all exhibited a slightly decreased effect.

Study on low temperature toughness and crystallization behavior of polypropylene random copolymer

2017 ◽  
Vol 37 (7) ◽  
pp. 715-727 ◽  
Author(s):  
Yingchun Li ◽  
Shuai He ◽  
Hui He ◽  
Peng Yu ◽  
Dongqing Wang
Keyword(s):  
Low Temperature ◽  
Crystallization Behavior ◽  
Annealing Treatment ◽  
Random Copolymer ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Polyolefin Elastomer ◽  
The Matrix ◽  
Low Temperature Toughness ◽  
Polymorphic Composition

Abstract This research designed a series of novel approaches aiming to tackle a long-standing problem that is the brittleness of polypropylene (PP) random copolymer (PPR) at low temperature. By introducing polyolefin elastomer (POE), the toughness of PPR was improved; talc improved the stiffness of PPR, low density polyethylene (LDPE) or high density PE (HDPE) improved the low temperature toughness of PPR, and annealing treatment also improved the low temperature toughness of PPR significantly. The addition of dicumyl peroxide (DCP) and triallyl isocyanurate (TAIC) increased its stiffness through the formation of cross-linking networks. Also, the crystallization behavior and morphology were investigated in detail. Differential scanning calorimetry (DSC) results indicated that the adoption of annealing treatment can improve the crystallinity of PPR, while a polarizing microscope revealed that the incorporation of foreign matter can facilitate the crystallization process of the matrix. X-ray diffraction (XRD) tests showed an unchanged polymorphic composition of PPR after introducing different additives, and scanning electron microscopy (SEM) indicated that annealing treatment can enhance interfacial interactions between the matrix and fillers.

scholarly journals Effect of the thermal annealing on the phase transitions of biogenic CaCO3 nanostructures

2019 ◽  
Vol 63 (1) ◽  
Author(s):  
Candelario Ramón de los Santos ◽  
Angélica Silvestre López Rodríguez ◽  
Pio Sifuentes Gallardo ◽  
Miguel Angel Hernández Rivera ◽  
German Pérez-Hernández ◽  
...  
Keyword(s):  
Calcium Hydroxide ◽  
Thermal Annealing ◽  
Annealing Treatment ◽  
Orthorhombic Phase ◽  
Natural State ◽  
X Ray Diffraction ◽  
X Ray ◽  
Air Atmosphere ◽  
Thermal Annealing Treatment ◽  
Two Phases

The issue of the present research lays its foundation on the proposal of the Crassostrea virginica waste oyster shells (WOS) reuse to obtain calcium carbonate powder (CaCO3) and calcium hydroxide (Ca(OH)2) nanostructured, using thermal annealing treatments. The oysters shells were subjected to a previous physical grinding process to decrease their size (smaller sizes 0.074 mm). The parameter studied was the effect of annealing temperature (500, 700 and 900 °C in air atmosphere) on the structural properties and morphology of the powders by FTIR, XRD, SEM and HRTEM. The X-ray diffraction results indicate that the WOS in their natural state and thermally annealed at 500 °C  have two phases of CaCO3 the rhombohedral form for calcite with crystallite size around 24 nm and aragonite traces in orthorhombic phase. At 700 °C, the WOS powder is transformed into calcium hydroxide, also known as portlandite (Ca(OH)2), attributed to the absorption of water released during the thermal decomposition of CaCO3. This crystalline phase does not change when the temperature increases to 900 °C. The SEM and HRTEM analysis of WOS powders reveals that with a thermal annealing treatment it is possible to obtain   nanostructured CaCO3. FTIR analysis demonstrates the biogenic origin of CaCO3, due to amide groups. The nanostructured CaCO3 obtained by grinding and thermal annealing of WOS, can be used as drying agent, or as additive in ceramic and glass. The issue of the present research lays its foundation on the proposal of the Crassostrea virginica waste oyster shells (WOS) reuse to obtain calcium carbonate powder (CaCO3) and calcium hydroxide (Ca(OH)2) nanostructured, using thermal annealing treatments. The oysters shells were subjected to a previous physical grinding process to decrease their size (smaller sizes 0.074 mm). The parameter studied was the effect of annealing temperature (500, 700 and 900 °C in air atmosphere) on the structural properties and morphology of the powders by FTIR, XRD, SEM and HRTEM. The X-ray diffraction results indicate that the WOS in their natural state and thermally annealed at 500 °C  have two phases of CaCO3 the rhombohedral form for calcite with crystallite size around 24 nm and aragonite traces in orthorhombic phase. At 700 °C, the WOS powder is transformed into calcium hydroxide, also known as portlandite (Ca(OH)2), attributed to the absorption of water released during the thermal decomposition of CaCO3. This crystalline phase does not change when the temperature increases to 900 °C. The SEM and HRTEM analysis of WOS powders reveals that with a thermal annealing treatment it is possible to obtain   nanostructured CaCO3. FTIR analysis demonstrates the biogenic origin of CaCO3, due to amide groups. The nanostructured CaCO3 obtained by grinding and thermal annealing of WOS, can be used as drying agent, or as additive in ceramic and glass.

scholarly journals Crystal Structures and Thermal Properties of L-MnC4H4O6•2H2O and DL-MnC4H4O6•2H2O

2019 ◽  
Vol 12 (1) ◽  
pp. 78
Author(s):  
Takanori Fukami ◽  
Shuta Tahara ◽  
Arbi Dimyati
Keyword(s):  
Thermal Analysis ◽  
Differential Scanning Calorimetry ◽  
Room Temperature ◽  
Structural Parameters ◽  
Silica Gels ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Weight Losses ◽  
Group Symmetries

Manganese L-tartrate dihydrate, L-MnC4H4O6·2H2O, and manganese DL-tartrate dihydrate, DL-MnC4H4O6·2H2O, crystals were grown at room temperature by the gel method using silica gels as the growth medium. Differential scanning calorimetry, thermogravimetric-differential thermal analysis, and X-ray diffraction measurements were performed on both crystals. The space group symmetries (monoclinic P21 and P2/c) and structural parameters of the crystals were determined at room temperature. Both structures consisted of slightly distorted MnO6 octahedra, C4H4O6 and H2O molecules, and O–H···O hydrogen-bonding frameworks between adjacent molecules. Weight losses due to thermal decomposition of the crystals were found to occur in the temperature range of 300–1150 K. We inferred that the weight losses were caused by the evaporation of bound 2H2O molecules, and the evolutions of gases from C4H4O4 and of (1/2)O2 gas from MnO2, and that the residual black substance left in the vessels after decomposition was manganese oxide (MnO).

Effect of Cooling Rates on the Solidification and Microstructure of Rapidly Solidified Mg70.8Zn28Nd1.2 Quasicrystal Alloy

2017 ◽  
Vol 898 ◽  
pp. 246-253
Author(s):  
Xing Jing Ge ◽  
Xin Ying Teng ◽  
Shu Min Xu ◽  
Jin Yang Zhang
Keyword(s):  
Electron Microscopy ◽  
Phase Transition ◽  
Thermal Analysis ◽  
Energy Dispersive Spectrometer ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Cooling Rates ◽  
X Ray ◽  
Rapidly Solidified ◽  
Scanning Electron

The influence of cooling rates on the solidification and microstructure of rapidly solidified quasicrystal alloy Mg70.8Zn28Nd1.2(at.%) was investigated. The microstructure, phase constitution, phase transition and phase structure of the alloys were examined by means of scanning electron microscopy, x-ray diffraction, energy dispersive spectrometer, differential scanning calorimetry. The experimental results showed that the phase composition of as-cast Mg70.8Zn28Nd1.2 alloy includes quasicrystal I-phase and Mg7Zn3 phase. For the rapidly solidified alloy ribbons, when the speed is not higher than 400 r/min, the microstructure includes I-phase, Mg7Zn3 phase and α-Mg phase. When the speed is at the range of 400-2000r/min, the Mg7Zn3 phase disappears and only quasicrystal with α-Mg phase exist. With the increase of cooling rate, the grain size decreases and there are a large number of microcrystals in the microstructure. When the speed reaches higher than 2500 r/min, amorphous phase appeared. Differential thermal analysis showed that quasicrystal exist at about 340°C.

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