Retraction notice to “Prediction total specific pore volume of geopolymers produced from waste ashes by ANFIS” [Ceram. Int. 38 (2012) 3111–3120]

Author(s):  
Ali Nazari ◽  
Gholamreza Khalaj ◽  
Shadi Riahi ◽  
Hamid Bohlooli ◽  
Mohammad Mehdi Kaykha
2015 ◽  
Vol 2015 ◽  
pp. 1-11 ◽  
Author(s):  
Hyunho Shin ◽  
Jun-Ho Eun

A TiC powder is synthesized from a micron-sized mesoporous metatitanic acid-sucrose precursor (precursor M) by a carbothermal reduction process. Control specimens are also prepared using a nanosized TiO2-sucrose precursor (precursor T) with a higher cost. When synthesized at 1500°C for 2 h in flowing Ar, the characteristics of the synthesized TiC from precursor M are similar to those of the counterpart from precursor T in terms of the crystal size (58.5 versus 57.4 nm), oxygen content (0.22 wt% versus 0.25 wt%), and representative sizes of mesopores: approximately 2.5 and 19.7–25.0 nm in both specimens. The most salient differences of the two specimens are found in the TiC from precursor M demonstrating (i) a higher crystallinity based on the distinctive doublet peaks in the high-two-theta XRD regime and (ii) a lower specific surface area (79.4 versus 94.8 m2/g) with a smaller specific pore volume (0.1 versus 0.2 cm3/g) than the counterpart from precursor T.


Soil Research ◽  
1990 ◽  
Vol 28 (6) ◽  
pp. 869 ◽  
Author(s):  
D Mcgarry

Differences in growth, yield and root systems of two adjoining cotton crops on a Vertisol near Dalby, Queensland, were explained in terms of soil profile morphology and soil shrinkage indices. The soil beneath the strongly inferior crop had platy structure in the 0.05-0.28 m layer and significantly less air-filled specific pore volume in the 0.2-0.4 m layer. This soil structure degradation was caused by seedbed preparation of wet soil, prior to sowing the cotton crop.


Soil Research ◽  
1990 ◽  
Vol 28 (6) ◽  
pp. 869
Author(s):  
D Mcgarry

Differences in growth, yield and root systems of two adjoining cotton crops on a Vertisol near Dalby, Queensland, were explained in terms of soil profile morphology and soil shrinkage indices. The soil beneath the strongly inferior crop had platy structure in the 0.05-0.28 m layer and significantly less air-filled specific pore volume in the 0.2-0.4 m layer. This soil structure degradation was caused by seedbed preparation of wet soil, prior to sowing the cotton crop.


2020 ◽  
Vol 4 (1) ◽  
pp. 6
Author(s):  
Michael Ioelovich

In this research, fractal properties of a cell wall in growing cotton fibers were studied. It was found that dependences of specific pore volume (P) and apparent density (ρ) on the scale factor, F = H/h, can be expressed by power-law equations: P = Po F(Dv−E) and ρ = ρo F(E−Dρ), where h is minimum thickness of the microfibrilar network in the primary cell wall, H is total thickness of cell wall in growing cotton, Dv = 2.556 and Dρ = 2.988 are fractal dimensions. From the obtained results it follows that microfibrilar network of the primary cell wall in immature fibers is loose and disordered, and therefore it has an increased pore volume (Po = 0.037 cm3/g) and low density (ρo = 1.47 g/cm3). With enhance days post anthesis of growing cotton fibers, the wall thickness and density increase, while the pore volume decreases, until dense structure of completely mature fibers is formed with maximum density (1.54 g/cm3) and minimum pore volume (0.006 cm3/g). The fractal dimension for specific pore volume, Dv = 2.556, evidences the mixed surface-volume sorption mechanism of sorbate vapor in the pores. On the other hand, the fractal dimension for apparent density, Dρ = 2.988, is very close to Euclidean volume dimension, E = 3, for the three-dimensional space.


2016 ◽  
Vol 70 (1) ◽  
pp. 9-19
Author(s):  
Danijela Maksin ◽  
Aleksandra Nastasovic ◽  
Tatjana Maksin ◽  
Zvjezdana Sandic ◽  
Katja Loos ◽  
...  

Synthesis of an unconventional resin based on 4-vinylpyridine (4-VP) and its Cu(II) sorption behavior were studied. Three samples of macroporous crosslinked poly(4-vinylpyridine-co-ethylene glycol dimethacrylate) [P4VPE] with different porosity parameters were prepared by suspension copolymerization by varying the n-heptane amount in the inert component. The samples were characterized by mercury porosimetry, elemental analysis and x-ray photoelectron spectroscopy (XPS). The sorption of P4VPE for Cu(II) ions, determined under non-competitive conditions, was relatively rapid, i.e. the maximum capacity was reached within 30 min. The maximum experimental sorption capacity for the sample with the highest values of pore diameter and specific pore volume (Sample 3, Qeq = 89 mg g-1) was 17.5 times higher than for the sample with the lowest values of pore diameter and specific pore volume (Sample 1, Qeq = 5.1 mg g-1). Since the values for pyridine content in all P4VPE samples were almost the same, it was concluded that the porosity parameters have predominant influence on Cu(II) sorption rates on P4VPE. The sorption behavior and the rate-controlling mechanisms were analyzed using six kinetic models (pseudo-first order, pseudo-second order, Elovich, intraparticle diffusion, Bangham and Boyd models). XPS study clarified the nature of the formed P4VPE-Cu(II) species.


2020 ◽  
Vol 22 (3) ◽  
pp. 157
Author(s):  
A. Nurgain ◽  
M. Nazhipkyzy ◽  
A.A. Zhaparova ◽  
A.T. Issanbekova ◽  
M. Alfe ◽  
...  

In this work, the effect of acid pre-treatment (hydrochloric acid, HCl) and calcination of diatomite, a silicon dioxide-material from natural sources, was studied with the aim to obtain diatomite-based sorbents with specific physicochemical properties. For this, acid pre-treatments with HCl at different calcination conditions, namely HCl concentration (0.5, 1 M) and calcination temperatures (from 600 to 900 °C) were studied. Morphological features different from those of natural diatomite were obtained. It has been found that treatment of diatomite with 0.5 M HCl at 800 °C showed a specific pore volume of 0.008 cm3/g, and a specific surface area of 19.26 m2/g, while the treatment of diatomite with 1.0 M HCl showed a specific pore volume of 0.011cm3/g, and a specific surface area of 25.57 m2/g. The performance of the acid pretreatment of diatomite for adsorption of Pb ions from water was also studied.


Author(s):  
Claudiu Valentin Suciu

Development of intelligent and ecological energy absorption systems (EAS) is important to various fields such as automotive (vehicle suspensions, bumpers, engine mounts), construction (protections against seismic and wind-induced vibrations), and defense (parachuted objects, armors). Usual EAS use composites, shape-memory alloys and foams. Recently, liquid adsorption/desorption in/from nanoporous solids was employed to develop high-performance nano-EAS. Energy loss is based on the well-known capillary phenomenon: external work must be done to spread a non-wetting liquid on a solid surface. Nano-EAS provide considerably higher dissipated energies, about 1–10J/g at deformability of 30–70%, compared with the energy absorption of Ti-Ni alloys, about 0.01–0.05J/g at deformability of 5–8%. For water against hydrophobic nanoporous silica gel (artificial sand), the nano-EAS become ecological; they can be also made intelligent by thermo-electrical control. Relative to thermal effects, Qiao et al. have investigated, for nanoporous silica gel with insufficient coverage of the alkyl-based hydrophobic coating, the problem of hysteresis recovery by increasing the temperature in the range 20∼80°C. Energy loss capacity reduced severely after the first loading-unloading cycle, so, the hysteresis was found as irreversible. Shape of the first hysteresis, the accessible specific pore volume and the desorption pressure were almost unaffected by the temperature change. At temperature augmentation the second hysteresis was partially recovered and when the temperature exceeded 50°C the system became almost fully reusable. Water inflow was found as governed by Laplace-Washburn equation but the outflow process was perceived as thermally aided. On the other hand, Eroshenko et al. have contradictorily obtained for nanoporous silica gel with full coverage of the alkyl-based hydrophobic coating, a stable hysteresis at repeated working cycles. Adsorption pressure decreased and desorption pressure increased at temperature augmentation, this producing a reduction of the hysteresis area and damping. However, the accessible specific pore volume was found as thermally unaffected. Oppositely, both the in- and out-flows were found as governed by Laplace-Washburn equation. In this work, for nanoporous silica gels with partial and full coverage of the alkyl and fluorocarbon based hydrophobic coatings, the thermal effects on the hysteresis and damping performances are studied. Test rig used is a compression-decompression chamber introduced inside of an incubator that allows temperature adjustment in the range of −10∼50°C. Results reveal that, depending on the hydrophobic coating coverage, findings reported by Qiao et al. and Eroshenko et al. are in fact not contradictory but complementary. However, as expected, the accessible specific pore volume was found to decrease at temperature reduction. In order to explain all these apparently opposite experimental findings, a model based on the water cluster size distribution versus temperature, the pore size distribution of silica gel and the ability of water molecules to form hydrogen bonds with the uncovered hydroxyl groups on the solid surface is proposed.


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