Pure ices IV and XII from high-density amorphous ice

2003 ◽  
Vol 81 (1-2) ◽  
pp. 25-32 ◽  
Author(s):  
C G Salzmann ◽  
I Kohl ◽  
T Loerting ◽  
E Mayer ◽  
A Hallbrucker

High-density amorphous ice (HDA), made by compression of hexagonal ice at 77 K, was heated at a constant pressure of 0.81 GPa up to 183 K and its phase transition followed by displacement-temperature curves. The crystalline phases, recovered at 77 K and 1 bar, were characterized by X-ray diffraction. Pure D2O ice IV and nearly pure H2O ice IV were formed on slow heating at a rate of 0.4 K min–1, whereas pure H2O ice XII and D2O ice XII were formed on fast heating at [Formula: see text] 15 K min–1. On heating HDA at rates in between these two values a mixture of ice IV and ice XII was obtained, where their relative yields depended in a systematic manner on the heating rate. Conversion of HDA into either ice IV or ice XII is an example of a "parallel reaction" where the relative yields of ice IV and ice XII can be controlled by temperature, i.e., by the rate of heating, in our approach. It is conceivable that a similar behaviour occurs on crystallization of the related pressure-amorphized silica. PACS Nos.: 61.10-i, 64.60-i, 64.70-p

2020 ◽  
Author(s):  
Chi-Toan Nguyen ◽  
Alistair Garner ◽  
Javier Romero ◽  
Antoine Ambard ◽  
Michael Preuss ◽  
...  

2021 ◽  
Vol 68 ◽  
pp. 1-16
Author(s):  
Cheng Zhang ◽  
Qing Shan Gao ◽  
Lu Yun Jiao ◽  
Laura Bogen ◽  
Nicole Forte ◽  
...  

Hollow graphitic porous carbon nanosphere (CNS) materials are synthesized from polymerization of resorcinol (R) and formaldehyde (F) in the presence of templating iron polymeric complex (IPC), followed by carbonization treatment. The effect of rapid heating in the carbonization process is investigated for the formation of hollow graphitic carbon nanospheres. The resulting CNS from rapid heating was characterized for its structure and properties by transmission electron microscope (TEM), x-ray diffraction (XRD), Raman spectroscopy, bulk conductivity measurement and Brunauer-Emmett-Teller (BET) surface area. Hollow graphitic CNS with reduced degree of agglomeration is observed under rapid heating during the carbonization process when compared to the CNS synthesized using the standard slow heating approach. Key words: carbon nanosphere (CNS), rapid pyrolytic carbonization, agglomeration


2019 ◽  
Vol 53 (15) ◽  
pp. 2091-2104 ◽  
Author(s):  
Gaurav Arora ◽  
Himanshu Pathak ◽  
Sunny Zafar

Carbon nanotubes have been used as reinforcements in polymers due to their high elasticity, flexibility, and thermal conductivity. In this study, pellets of high-density polyethylene +20 wt% carbon nanotube and polypropylene +20 wt% carbon nanotube were cured using microwave energy. X-ray diffraction, differential scanning calorimetry, thermogravimetric analysis, uniaxial tensile test, and scanning electron microscopy was used to study morphology, thermal stability, and mechanical performance of the microwave-cured composites. X-ray diffraction analysis confirmed the bonding between the polymer and carbon nanotube as the peaks shifted and intensified. From the thermal study, it was observed that melting point of the composites is affected by microwave curing and the crystallinity of high-density polyethylene/carbon nanotube and polypropylene/carbon nanotube changed by 57.67% and 47.28%, respectively. Results of the uniaxial tensile test indicated that Young’s modulus of microwave cured high-density polyethylene/carbon nanotube and polypropylene/carbon nanotube composites were improved by 295% and 787.8%, respectively. Scanning electron microscopic fractography shows the stretching of polymer over-lapped on carbon nanotubes in the direction of the applied load.


Author(s):  
Daniel Mariedahl ◽  
Fivos Perakis ◽  
Alexander Späh ◽  
Harshad Pathak ◽  
Kyung Hwan Kim ◽  
...  

Here we report about the structural evolution during the conversion from high-density amorphous ices at ambient pressure to the low-density state. Using high-energy X-ray diffraction, we have monitored the transformation by following in reciprocal space the structure factor S OO ( Q ) and derived in real space the pair distribution function g OO ( r ). Heating equilibrated high-density amorphous ice (eHDA) at a fast rate (4 K min –1 ), the transition to the low-density form occurs very rapidly, while domains of both high- and low-density coexist. On the other hand, the transition in the case of unannealed HDA (uHDA) and very-high-density amorphous ice is more complex and of continuous nature. The direct comparison of eHDA and uHDA indicates that the molecular structure of uHDA contains a larger amount of tetrahedral motives. The different crystallization behaviour of the derived low-density amorphous states is interpreted as emanating from increased tetrahedral coordination present in uHDA. This article is part of the theme issue ‘The physics and chemistry of ice: scaffolding across scales, from the viability of life to the formation of planets'.


Energies ◽  
2020 ◽  
Vol 13 (23) ◽  
pp. 6359
Author(s):  
Elena David

Conversion experiments of wet and dry walnut shells were performed, the influence of moisture content on the hydrogen yield in the gas fraction was estimated and the resulted biochar structure was presented. Measurements of the biochar structures were performed using X-ray diffraction and scanning electron microscopy methods. The results demonstrate that heating rate played a key role in the pyrolysis process and influenced the biochar structure. Under fast heating rate, the interactions between the water vapors released and other intermediate products, such as biochar was enhanced and consequently more hydrogen was generated. It could also be observed that both biochar samples, obtained from wet and dry walnut shells, had an approximately smooth surface and are different from the rough surface of the raw walnut shell, but there are not obvious differences in shape and pores structure between the two biochar samples. The increasing of the biochar surface area versus pyrolysis temperature is due tothe formation of micropores in structure. The biochar shows a surface morphology in the form of particles with rough, compact and porous structure. In addition the biochar structure confirmed that directly pyrolysis of wet walnut shells without predried treatment has enhanced the hydrogen content in the gas fraction.


2003 ◽  
Vol 18 (1) ◽  
pp. 166-172 ◽  
Author(s):  
Kun'ichi Miyazawa ◽  
Minoru Akaishi ◽  
Yusuke Kuwasaki ◽  
Tadatomo Suga

Structural, mechanical, and electrical properties were examined for C60 whiskers, high-pressure sintered C60 whiskers, and C60 powder. A high density of dislocations was observed in the C60 whiskers, and the C60 whiskers with diameters of a few hundred nanometers were found to be flexible. Although both the specimens sintered under the same condition showed similar surface x-ray diffraction profiles with a strong accumulation of [110]tr orientation, the sintered C60 whiskers showed a higher micro-Vickers hardness and an electrical resistivity four orders of magnitude lower than that of the sintered C60 powder.


1983 ◽  
Vol 21 (3) ◽  
pp. 329-352 ◽  
Author(s):  
Robert J. Cembrola ◽  
Thein Kyu ◽  
Richard S. Stein ◽  
Shoji Suehiro ◽  
Hiromichi Kawai

1978 ◽  
Vol 21 (85) ◽  
pp. 629-638
Author(s):  
T. Hondoh ◽  
A. Higashi

AbstractLarge-angle tilt grain boundaries in artificially-grown ice bicrystals were observed by the method of X-ray diffraction topography. In bicrystals for which misorientation angles satisfy the conditions of a high-density coincidence site lattice (CSL) at the boundary, the images of fine parallel line defects appear on the topograph taken immediately after a light deformation. Since these images disappear in a time period between several hours and a few days and reappear again at the same sites when the specimen is deformed subsequently, it is concluded that these line defects are not stable like the boundary dislocations but may be steps generated on the boundary to form facets which coincide with the high-density CSL plane. X-ray topographic images of boundaries which do not satisfy the conditions of a high density CSL are complex and difficult to interpret, although some of the images indicate that there may be different types of structures on such boundaries.


2006 ◽  
Vol 312 ◽  
pp. 187-192 ◽  
Author(s):  
S.P. Bao ◽  
Sie Chin Tjong

High density polyethylene (HDPE)/organoclay nanocomposites toughened with maleated styrene-ethylene-butylene-styrene elastomer (SEBS-g-MA) were prepared by melt compounding. The structure and mechanical properties of such nanocomposites were investigated by X-ray diffraction (XRD), Fourier transform infrared spectrometry (FTIR), tensile and impact techiniques. XRD measurements showed that meleic anhydride group of SEBS elastomer was beneficial in forming an intercalated or partially exfoliated structure. The essential work of fracture (EWF) approach under tensile condition was used to characterize the fracture toughness of nanocomposites. The results indicated that the addition of SEBS-g-MA to the HDPE/organoclay nanocomposites greatly enhanced their fracture toughness.


2013 ◽  
Vol 37 (1) ◽  
pp. 11-20 ◽  
Author(s):  
Nasrin Parvin ◽  
Md Samir Ullah ◽  
Md Forhad Mina ◽  
Md Abdul Gafur

Organic filler like carbon black (CB) and inorganic filler like talc (T) with 0, 0.5, 1.0, 10, 20 and 40 wt% were separately loaded in high density polyethylene (HDPE) by the extrusion moulding method at 160oC. Then, different sets of filler loaded HDPE composites were prepared using the compression moulding technique, and their structures and mechanical properties were characterized. The pure HDPE sample, as examined by the X-ray diffraction (XRD) technique, showed orthorhombic structure, which did not change either with filler types or with their concentration. The only variations found in the structure are the changes of crystallinity and crystallized size that depend on both types of fillers and their concentrations. Incorporation of CB in HDPE emphasizes the crystallinity and crystallized size more than that of T. The tensile strength of the composite decreases with the increase of both types of fillers, and this decrease is explained on the basis of Nielson model, which basically describes a poor interaction between filler and HDPE matrix. An increase of Young’s modulus of 350% is observed with the increasing CB and T contents, representing an increase of the stiffness in the materials. Flexural strength increased with the increase of CB content but decreased with the increase of talc content. Although the microhardness was observed to increase with both types of fillers, the hardness value was 80% higher for CB loaded-composites than that of T at 40 wt% filler content. These findings strongly indicate that the compatibility of HDPE is better with organic filler than with inorganic one. DOI: http://dx.doi.org/10.3329/jbas.v37i1.15675 Journal of Bangladesh Academy of Sciences, Vol. 37, No. 1, 11-20, 2013


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