scholarly journals Experimental Study on Influence of Vaporous Water on Salt Expansion of Sulfate Saline Soil

2019 ◽  
Vol 2019 ◽  
pp. 1-9 ◽  
Author(s):  
Shuquan Peng ◽  
Fan Wang ◽  
Ling Fan

The harm of salt expansion of saline soil in arid areas has always been a major problem to be solved urgently. According to the conversion rule between sodium sulfate and sodium sulfate decahydrate, sodium sulfate decahydrate crystals can be precipitated from sodium sulfate solution by cooling. Besides, when the relative humidity (RH) exceeds the critical relative humidity (CRH), sodium sulfate decahydrate can be formed by the combination of sodium sulfate and vaporous water, resulting in the salt volume expansion. However, at present, in the salt expansion mechanism of sulfate saline soil, only the influence of liquid water is considered while vaporous water is not involved. To study the effects of temperature, salinity, and ARH on salt expansion, the salt expansion test of dry sulfate saline soil under the action of vaporous water was conducted, and its composition was analyzed by X-ray diffraction (XRD) technology. Experimental results showed that sodium sulfate decahydrate crystals were produced in the sulfate saline soil if the relative humidity (RH) of pore gas exceeded the critical one so that salt expansion occurred. Salt expansion and salt expansion rate of sulfate saline soil increased with the increase of RH and salinity but decreased with the increase of temperature. Therefore, the new salt expansion mechanism of sulfate saline soil under vaporous water is verified. The experimental results further perfected the original salt expansion mechanism of sulfate saline soil under the action of liquid water and guided the study of new treatment methods of sulfate saline soil.

2021 ◽  
Vol 2021 ◽  
pp. 1-17
Author(s):  
Yanjie Ji ◽  
Xu Li ◽  
Wei Wang ◽  
Li Liu

The salt expansion disease is severe for the soil containing sodium sulfate in cold regions. This paper carried out one-dimensional salt expansion tests of saline soil, the crystallization test of saturated sodium sulfate solution, and the numerical cooling tests to explore the stability time of the salt expansion test and determine the standard procedure of salt expansion tests. The test results demonstrate that (i) the temperature equilibrium and the crystallization process are almost simultaneously completed in both sulfate saline soil and sulfate solution upon cooling; (ii) referring to the deformation equilibrium standard used in soil consolidation test, an expansion rate of less than 0.02 mm/h is suggested in the saline expansion test; and (iii) the equilibrium time is found to have a quadratic polynomial relationship to sample size and is much shorter under liquid bath conditions than under gas bath conditions. Based on these findings, a standard procedure of the one-dimensional salt expansion test is proposed, in which the test equipment, the test process, the deformation stabilization time of salt expansion, and the data processing method are provided. As the deformation and the temperature are synchronized, the deformation stabilization time of samples with different sizes in different cooling media is recommended.


2019 ◽  
Vol 24 (4) ◽  
Author(s):  
Sâmea Valensca Alves Barros ◽  
Gelmires de Araújo Neves ◽  
Romualdo Rodrigues Menezes ◽  
Gerbeson Carlos Batista Dantas ◽  
Patrícia Mendonça Pimentel

ABSTRACT The residues of ornamental rocks, especially quartzite, cause great environmental impact. More impulse has been given to research on the recycling of these residues over the last years, particularly for use as aggregates in concrete and mortar. Nevertheless, the studies conducted so far do not mention the behavior of the mortar blended with aggregates coming from residues of ornamental rocks when under chemical attacks in sulfate-rich environment. Thus, in the present study it was sought to add quartzite residues to the mortar, verifying its mechanical behavior and its durability when attacked by sodium sulfate (Na2SO4). The durability of the mortar blended with quartzite residues under sulfate attack was evaluated by the dimensional variation of the test specimens when immersed in sodium sulfate solution, according to the methodology of the NBR 13583 standard. Were used the following complementary techniques: simple compressive strength, X-ray diffraction and thermogravimetric and differential analysis. From the tests, it was verified that the mortars, after attack of sodium sulfate, presented dimensional expansions superior to 0.06%, as well as increased mechanical strength. Therefore, although it was found that the specimens incorporated with quartzite residues were attacked by sulfate, it was observed that it was not able to form sufficient secondary ettringite to mechanically damage the specimens submitted to the sodium sulfate attack.


2015 ◽  
Vol 2015 ◽  
pp. 1-10 ◽  
Author(s):  
Kwang-Myong Lee ◽  
Su-Ho Bae ◽  
Jae-Im Park ◽  
Soon-Oh Kwon

The present study suggested a mass change prediction model for sulfate attack of concrete containing mineral admixtures through an immersion test in sulfate solutions. For this, 100% OPC as well as binary and ternary blended cement concrete specimens were manufactured by changing the types and amount of mineral admixture. The concrete specimens were immersed in fresh water, 10% sodium sulfate solution, and 10% magnesium sulfate solution, respectively, and mass change of the specimens was measured at 28, 56, 91, 182, and 365 days. The experimental results indicated that resistance of concrete containing mineral admixture against sodium sulfate attack was far greater than that of 100% OPC concrete. However, in terms of resistance against magnesium sulfate attack, concrete containing mineral admixture was lower than 100% OPC concrete due to the formation of magnesium silicate hydrate (M-S-H), the noncementitious material. Ultimately, based on the experimental results, a mass change prediction model was suggested and it was found that the prediction values using the model corresponded relatively well with the experimental results.


2020 ◽  
Vol 1000 ◽  
pp. 436-446
Author(s):  
Bambang Suharno ◽  
Nolzha Primadha Ilman ◽  
Achmad Shofi ◽  
Deni Ferdian ◽  
Fajar Nurjaman

This study was conducted to investigate the effect of palm shell charcoal reductant in the selective reduction of nickel ore with the addition of additive at various temperatures and times. In this present work, 10 wt. % of sodium sulfate as additive and 5, 10, 15 wt. % of palm shell charcoal as reductants were used. The reduction of nickel ore was performed at 950oC, 1050oC, and 1150oC for 60, 90, and 120 minutes. A wet magnetic separation method was then carried out to separate the concentrates and tailings. Characterization of reduced ore was performed by X-Ray Diffraction (XRD) and Scanning Electron Microscope (SEM) with Energy Dispersive X-ray Spectroscopy (EDS), while the composition of ferronickel in concentrate was identified by X-Ray Fluorescence (XRF). The result showed that the higher temperature reduction, the higher of nickel grade, and its recovery at the concentrate. Nevertheless, the longer reduction time and the more reductant in nickel ore lowering the nickel grade and its recovery in the concentrate. The optimum condition in this selective reduction process was obtained with the addition of 5 wt. % of reductant and 10 wt. % of sodium sulfate in nickel ore, which was reduced at 1150oC for 60 minutes. It resulted in 4.60% and 73.23% for nickel grade and its recovery, respectively.


2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Lijun Cheng ◽  
Yong Kang ◽  
Guishui Li

Difference between adsorption of benzene by diatomite and nano-TiO2immobilized on diatomite was investigated. And effects of temperature, light intensity, relative humidity, and initial benzene concentration on adsorption and degradation of benzene by nano-TiO2immobilized on diatomite were also studied. The experimental results showed that when initial benzene concentration was2.2×10−3 mg L−1, it could be degraded to below safe concentration (1.1×10−4 mg L−1) after 50 h when temperature was 20°C, but it just needed 30 h at 35°C. When light intensity was 6750 Lx, it needed 30 h for benzene to be degraded to below safe concentration, but benzene could barely be degraded without light. When relative humidity was 50%, benzene could be degraded to1.0×10−4 mg L−1after 30 h, while its concentration could be reduced to7.0×10−5 mg L−1at the relative humidity of 80%.


2013 ◽  
Vol 31 (2) ◽  
pp. 139-156
Author(s):  
J.M.P.Q. Delgado ◽  
V.P. de Freitas ◽  
A.S. Guimarães ◽  
C. Ferreira

2021 ◽  
Vol 11 (5) ◽  
pp. 724-731
Author(s):  
Hemin Liu ◽  
Qian Huang ◽  
Liang Zhao

This study investigates the deterioration of concrete containing limestone powder exposed to sulfate solution under ambient temperature (20~25 °C). Microstructure and mineral phases within the attacked concrete were measured by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and X-ray diffraction (XRD). It was found that the addition of limestone powder increased the initial porosity of concrete. Consequently, a larger amount of SO2–4 ions diffused into the concrete containing limestone powder, and their degree of deterioration caused by sulfate attack increased with the increase in limestone powder content. At ambient temperature, gypsum and ettringite were the major attack products, respectively within the surface and nearsurface portions of concrete containing limestone powder, which was consistent with the products of sulfate attack within concrete without limestone powder. Therefore, the type and distribution of the attack products in concrete had not been revised due to the addition of limestone powder. Nevertheless, the adverse influence of limestone powder on the sulfate resistance of concrete, even at ambient temperature, should be considered. Furthermore, effective measures should be implemented to improve the durability of concrete containing limestone powder in this environment.


2004 ◽  
Vol 848 ◽  
Author(s):  
Evan Lyle Thomas ◽  
Erin E. Erickson ◽  
Monica Moldovan ◽  
David P. Young ◽  
Julia Y. Chan

AbstractA new member of the LnMIn5 family, ErCoIn5, has been synthesized by a flux-growth method. The structure of ErCoIn5 was determined by single crystal X-ray diffraction. It crystallizes in the tetragonal space group P4/mmm, Z = 1, with lattice parameters a = 4.5400(4) and c = 7.3970(7) Å, and V = 152.46(2) Å3. Electrical resistivity data show metallic behavior. Magnetic susceptibility measurements show this compound to be antiferromagnetic with TN = 5.1 K. We compare these experimental results with those of LaCoIn5 in an effort to better understand the effect of the structural trends observed on the transport and magnetic properties.


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