Performance and Application of Far Infrared Rays Emitted from Rare Earth Mineral Composite Materials

2008 ◽  
Vol 8 (3) ◽  
pp. 1203-1210 ◽  
Author(s):  
Jinsheng Liang ◽  
Dongbin Zhu ◽  
Junping Meng ◽  
Lijuan Wang ◽  
Fenping Li ◽  
...  
Keyword(s):  
Free Energy ◽  
Rare Earth ◽  
Composite Materials ◽  
Surface Free Energy ◽  
Dynamic Contact Angle ◽  
Far Infrared ◽  
Diesel Oil ◽  
Liquefied Petroleum Gas ◽  
X Ray ◽  
Rare Earth Mineral

Rare earth mineral composite materials were prepared using tourmaline and cerous nitrate as raw materials. Through characterization by scanning electron microscopy, X-ray diffraction, X-ray photo-electron spectroscopy, dynamic contact angle meter and tensiometer, and Fourier transform infrared spectroscopy, it was found that the composite materials had a better far infrared emitting performance than tourmaline, which depended on many factors such as material composition, microstructure, and surface free energy. Based on the results of the flue gas analyzer and the water boiling test, it was found that the rare earth mineral composite materials could accelerate the combustion of liquefied petroleum gas and diesel oil. The results showed that the addition of Ce led to the improvement of far infrared emitting performance of tourmaline due to the decrease of cell volume caused by the oxidation of more Fe2+ ions and the increase of surface free energy. The application of rare earth mineral composite materials to diesel oil led to a decrease in surface tension and flash point, and the fuel saving ratio could reach 4.5%. When applied to liquefied petroleum gas, the composite materials led to the enhanced combustion, improved fuel consumption by 6.8%, and decreased concentration of CO and O2 in exhaust gases by 59.7% and 16.2%, respectively; but the temperature inside the flue increased by 10.3%.

Effect of Nanometer Far-Infrared Materials on the Cleanability of Ceramic Glazes

2010 ◽  
Vol 178 ◽  
pp. 103-108
Author(s):  
Li Juan Wang ◽  
Jin Sheng Liang ◽  
Wen Bo Xu ◽  
Dao Yang Han
Keyword(s):  
Contact Angle ◽  
Free Energy ◽  
Oleic Acid ◽  
Surface Free Energy ◽  
Dynamic Contact Angle ◽  
Far Infrared ◽  
Dynamic Contact ◽  
Interface Tension ◽  
Static Contact ◽  
Infrared Materials

Nanometer far-infrared materials (NFIM) were doped into ceramic glazes to prepare easy-to-clean ceramic glazes，and the effect of NFIM on the cleanability properties was investigated. Static contact angle measurements were used to describe the surface hydrophilic property and calculate the surface free energy. The effect of far-infrared radiance measured by Fourier Transform Infrared Spectrometer on the O/W interface tension was tested by a Dynamic Contact Angle Meter and Tensiometer. The cleanability was estimated by the ultraviolet spectrophotometry technique using oleic acid as soiling agent. It was shown that the better cleanability of the ceramic glazes, the higher surface free energy and its polar contribution. The experiments were carried out on detachment of oleic acid drop from the easy-to-clean ceramic glazes. The three-phase contact line shrinked spontaneously, and eventually the oil drop detached from the surface. The spontaneous detachment of a drop corresponded to two different driving factors: (1) the decrease of oil-water interfacial tension caused by the far-infrared radiation of the glazes, (2) the spontaneous advancement of aqueous meniscus owing to the penetration of water between the oil and super hydrophilic glaze surfaces.

Performance and Application of Far Infrared Rays Emitted from Rare Earth Mineral Composite Materials

2008 ◽  
Vol 8 (3) ◽  
pp. 1203-1210 ◽  
Author(s):  
Jinsheng Liang ◽  
Dongbin Zhu ◽  
Junping Meng ◽  
Lijuan Wang ◽  
Fenping Li ◽  
...  
Keyword(s):  
Rare Earth ◽  
Composite Materials ◽  
Far Infrared ◽  
Infrared Rays ◽  
Rare Earth Mineral

Preparation and Characterization of Rare Earth Composite Materials Radiating Far Infrared for Activating Liquefied Petroleum Gas

2006 ◽  
Vol 24 (1) ◽  
pp. 277-280 ◽  
Author(s):  
Zhu Dongbin ◽  
Liang Jinsheng ◽  
Li Fenping ◽  
Ding Yan ◽  
Wang Lijuan ◽  
...  
Keyword(s):  
Rare Earth ◽  
Composite Materials ◽  
Far Infrared ◽  
Liquefied Petroleum Gas

Far Infrared Radiation Property of Rare Earth Mineral Composite Materials

2006 ◽  
Vol 24 (1) ◽  
pp. 281-283 ◽  
Author(s):  
Liang Jinsheng ◽  
Wang Lijuan ◽  
Xu Gangke ◽  
Meng Junping ◽  
Ding Yan
Keyword(s):  
Rare Earth ◽  
Composite Materials ◽  
Infrared Radiation ◽  
Far Infrared ◽  
Radiation Property ◽  
Rare Earth Mineral ◽  
Far Infrared Radiation

Kihlmanite-(Ce), Ce2TiO2[SiO4](HCO3)2(H2O), a new rare-earth mineral from the pegmatites of the Khibiny alkaline massif, Kola Peninsula, Russia

2014 ◽  
Vol 78 (3) ◽  
pp. 483-496 ◽  
Author(s):  
V. N. Yakovenchuk ◽  
S.V. Krivovichev ◽  
G. Y. Ivanyuk ◽  
Ya. A. Pakhomovsky ◽  
E.A. Selivanova ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Rare Earth ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
X Ray ◽  
Intimate Association ◽  
Mohs Hardness ◽  
Rare Earth Mineral ◽  
Alkaline Massif ◽  
Khibiny Alkaline Massif

AbstractKihlmanite-(Ce), Ce2TiO2[SiO4](HCO3)2(H2O), is a new rare-earth titanosilicate carbonate, closely related to tundrite-(Ce). It is triclinic, P, a = 4.994(2), b = 7.54(2), c = 15.48(4) Å, α = 103.5(4), β = 90.7(2), γ = 109.2(2)o , V = 533(1) Å3, Z = 2 (from powder diffraction data) or a = 5.009(5), b = 7.533(5), c = 15.407(5) Å, α = 103.061(5), β = 91.006(5), γ = 109.285(5)°, V = 531.8(7) Å3, Z = 2 (from single-crystal X-ray diffraction data). The mineral was found in the arfvedsonite-aegirine-microcline vein in fenitized metavolcanic rock at the foot of the Mt Kihlman (Chil’man), near the western contact of the Devonian Khibiny alkaline massif and the Proterozoic Imandra-Varzuga greenstone belt. It forms brown spherulites (up to 2 cm diameter) and sheaf-like aggregates of prismatic crystals, flattened on {010} and up to 0.5 mm diameter. Both spherulites and aggregates occur in interstices in arfvedsonite and microcline, in intimate association with golden-green tundrite-(Ce). Kihlmanite-(Ce) is brown, with a vitreous lustre and a pale yellowish-brown streak. The cleavage is perfect on {010}, parting is perpendicular to c and the fracture is stepped. Mohs hardness is ∼3. In transmitted light, the mineral is yellowish brown; pleochroism and dispersion were not observed. Kihlmanite-(Ce) is biaxial (+), α = 1.708(5), β = 1.76(1), γ = 1.82(1) (589 nm), 2Vcalc = 89°. The optical orientation is Y ^ c = 5°, other details are unclear. The calculated and measured densities are 3.694 and 3.66(2) g cm−3, respectively. The mean chemical composition, determined by electron microprobe, is: Na2O 0.13, Al2O3 0.24, SiO2 9.91, CaO 1.50, TiO2 11.04, MnO 0.26, Fe2O3 0.05, Nb2O5 2.79, La2O3 12.95, Ce2O3 27.33, Pr2O3 2.45, Nd2O3 8.12, Sm2O3 1.67, Gd2O3 0.49 wt.%, with CO2 15.0 and H2O 6.0 wt.% (determined by wet chemical and Penfield methods, respectively), giving a total of 99.93 wt.%. The empirical formula calculated on the basis of Si + Al = 1 atom per formula unit is (Ca0.16Na0.11Mn0.02)∑0.29[(Ce0.98La0.47Pr0.09Nd0.29Sm0.06Gd0.02)∑1.91(Ti0.82Nb0.12)∑0.94O2 (Si0.97Al0.03)∑1O4.02(HCO3)2.01](H2O)0.96. The simplified formula is Ce2TiO2(SiO4)(HCO3)2·H2O. The mineral reacts slowly in cold 10% HCl with weak effervescence and fragmentation into separate plates. The strongest X-ray powder-diffraction lines [listed as d in Å(I) (hkl)] are as follows: 15.11(100)(00), 7.508(20)(00), 6.912(12)(01), 4.993(14)(00), 3.563(15)(01), 2.896(15)(1). The crystal structure of kihlmanite-(Ce) was refined to R1 = 0.069 on the basis of 2441 unique observed reflections (MoKα, 293 K). It is closely related to the crystal structure of tundrite-(Ce) and is based upon [Ce2TiO2(SiO4)(HCO3)2] layers parallel to (001). Kihlmanite-(Ce) can be considered as a cationdeficient analogue of tundrite-(Ce). The mineral is named in honour of Alfred Oswald Kihlman (1858–1938), a remarkable Finnish geographer and botanist who participated in the Wilhelm Ramsay expeditions to the Khibiny Mountains in 1891–1892. The mineral name also reflects its occurrence at the Kihlman (Chil’man) Mountain.

Hydrophobic and Oleophilic Filter Paper for Oil/Water Separation

2019 ◽  
Vol 798 ◽  
pp. 385-390
Author(s):  
Sunisa Jindasuwan ◽  
Sitthisuntorn Supothina
Keyword(s):  
Contact Angle ◽  
Free Energy ◽  
Surface Free Energy ◽  
Water Contact Angle ◽  
Filter Paper ◽  
Diesel Oil ◽  
Selective Removal ◽  
Water Contact ◽  
Water Separation ◽  
Filter Papers

The separation of oil from water is significance for environmental de-pollution application. To obtain selectivity of liquid, filter papers were coated to bear highly hydrophobic and oleophilic functionality that can allow only oils to pass through them. The coating solutions were prepared by mixing poly(methylhydro siloxane, PMHS) and fumed silica at various proportions. To determine an optimum coating condition, properties of the treated filter papers were investigated by measuring water contact angle and surface free energy, examining surface morphology and testing for selective removal of diesel oil from water. The optimum coating solution was at the PMHS:fumed silica weight ratio of 1.25:1.00. The treated filter paper exhibited high hydrophobicity with water contact angle of 142.80 ± 0.36 degrees and surface free energy of 0.78 mJ/m2. In addition, it exhibited high selective removal of diesel oil from water with oil absorption capacity of 2.3 g/g.

New Aspects on Melting and Annealing Behaviour of Polymers

1978 ◽  
Vol 33 (12) ◽  
pp. 1472-1483
Author(s):  
J. Haase ◽  
S. Köhler ◽  
R. Hosemann
Keyword(s):  
Free Energy ◽  
Melting Point ◽  
Partial Melting ◽  
Surface Free Energy ◽  
Average Crystallite Size ◽  
X Ray ◽  
State Diffusion ◽  
Crystallite Sizes ◽  
Dta Curves ◽  
Dta Curve

Abstract Poly( 1-butene) (PB) crystallizes from the melt in a metastable modification II (mod. II) which slowly transforms into the stable modification I (mod. I). X-ray wide angle (WAXS) measurements show that in mod. I the size of the microparacrystallites (mPC’s) in chain direction, D̅012, the polydispersity gD of the size distribution in this direction, the lateral size D̅110 and the paracrystalline g110-value do not change upon annealing at temperatures up to the melting point. In mod. II, however, the sizes D̅012 and D̅110 increase with rising annealing temperature Tann. At a certain Tann and beyond a sufficient annealing time tann the size D̅012 shows a logarithmic increase with tann whereas D̅110 stays constant. Measuring melting points Tm of mod. I-samples, we found a linear relationship between Tm and 1/D̅012 according to the Thomson equation resulting in a melting point for an infinite crystal of Tm∞ (mod. I) = 139 °C and a mean surface free energy of σ̅e′̅ (mod. I) = 47 ergs/cm2. T m versus 1/D̅012 for mod. II is linear only for high D̅012-values yielding Tm∞ (mod. II) = 130 °C and σ̅e′̅ (mod. II) = 29 ergs/cm2. However, a partially molten and afterwards quenched sample of mod. I with small mPC’s shows a mod. II-peak which fits the straight line extrapolated from the large D̅012-values. The DTA curves of mod. I-samples shift to higher temperatures and narrow after annealing although the crystallite sizes and size distributions remain as well as the paracrystalline distortions the same. X-ray and DTA measurements eliminate therefore surface premelting and selective melting of thinner and more distorted lamellae in mod. I. Upon annealing this modification, σ̅e′̅ decreases from 47 ergs/cm2 to 15 ergs/cm2 and the distribution of σe′ narrows. The latter determines predominantly the shape of the DTA curve. The Thomson equation therefore, applied to different samples links only the average crystallite size and the mean surface free energy with the melting point. In mod. I partial melting occurs independent of D̅012 and starts mainly at those mPC’s which have exposed surfaces with high σe′. At the beginning only single mPC’s or single lamellae melt, but no bundles of lamellae. The logarithmic increase of D̅012 in mod. II with tann can be explained according to Hosemann’s model of “lateral melting” also by a partial melting of mPC’s with unprotected lateral surfaces and by a consecutive solid state diffusion of their chainsegments into the two mPC’s adjacent in chain direction, increasing the averaged sizes of the long period and the lamellae thickness.

The influence of X-rays on the stability of selected properties of polyethylene

2018 ◽  
Vol 23 (1) ◽  
pp. 3-11
Author(s):  
Anna Wiśniewska ◽  
Gabriela Chwalik ◽  
Sylwia Łagan
Keyword(s):  
Free Energy ◽  
Surface Free Energy ◽  
Living Organism ◽  
Degradation Process ◽  
Material Surface ◽  
Control Group ◽  
X Rays ◽  
X Ray ◽  
The Stability

The evaluation of a degradation process of polyethylene (PE) in in vitro conditions under the influence of X-rays (X) and an in-cubation in two solutions simulating the environment of a living organism (SBF – simulated body fluid) was carried out. A dose corresponding to 10 standard X-ray pictures of the skeletal system as well as Ringer's and saline solutions at 40°C were used in the study. The paper presents the results of the influence of the 12-month studies on the selected surface properties of the material: surface wettability and abrasiveness. The value of surface free energy (SFE) was determined on the basis of the wetting angle measurements. The conductivity of the incubation fluids was also analyzed. The obtained results indicate that the adopted dose of X-ray radiation has no significant effect on the wettability of the surface of polyethylene. The nature of the surface layer of polyethylene did not change as a result of the 12-month incubation and remained hydrophilic. For the samples incubated in both immersion fluids, a decrease in surface free energy (SFE) was observed. For both the irradiated material and the control group, no significant changes in the mass of the samples and the conductivity of the incubation fluids were found, which indicates the stability of polyethylene. However, the abrasion value increased by approximately 26%. With the passage of the incubation time, a decrease in the value of this parameter was observed for the polyethylene subjected to radiation. No significant changes were found for the control group.

scholarly journals Epoxyorganosilane Finishing Compositions for Fibrous Fillers of Thermosetting and Thermoplastic Binders

Polymers ◽  
2021 ◽  
Vol 14 (1) ◽  
pp. 59
Author(s):  
Alexey V. Shapagin ◽  
Natalia A. Gladkikh ◽  
Arkadiy A. Poteryaev ◽  
Valentina Yu. Stepanenko ◽  
Uliana V. Nikulova ◽  
...  
Keyword(s):  
Free Energy ◽  
Composite Materials ◽  
Surface Free Energy ◽  
Materials Science ◽  
Sessile Drop ◽  
Inert Atmosphere ◽  
Energy Characteristics ◽  
Urgent Task ◽  
Wide Range ◽  
Epoxy Systems

The development of universal finishing compositions for fibers of various natures is an urgent task for polymer composite materials science. The developed finishes can be used for the fiber reinforcement of polymer matrices with a wide range of surface free energy characteristics. Epoxy systems modified with diaminesilane in a wide concentration range were examined by optical interferometry, FTIR spectroscopy, DSC and the sessile drop technique. It was shown that the partial curing of epoxy resin by diaminesilane at room temperature under an inert atmosphere, followed by contact with air, leads to a significant increase of the surface free energy of the system. Varying the concentration of diaminesilane allows us to effectively regulate the surface free energy of the composition. This makes it possible to use fibers finished with epoxyaminosilane compositions in composite materials based on a various thermosetting and thermoplastic binders with a surface tension of up to 75 mJ/m2.

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