scholarly journals Protection of Stone Monuments Using a Brushing Treatment with Ammonium Oxalate

Coatings ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 379
Author(s):  
Domagoj Mudronja ◽  
Frederik Vanmeert ◽  
Stjepko Fazinic ◽  
Koen Janssens ◽  
Darko Tibljas ◽  
...  

Stone monuments and buildings are susceptible to weathering. Carbonate-based stones are especially vulnerable in acidic environments, whereas magmatic acidic stones are more susceptible to chemical weathering in basic environments. To slow down surface corrosion of limestone and marble artworks/buildings, protective coatings which inhibit calcite dissolution have been proposed. In this work, samples from two stone types with different porosity were treated with ammonium oxalate (AmOx) to create a protective layer of calcium oxalate (CaOx) using the previously developed brushing method. Two different synchrotron microscopy experiments were performed to determine its protective capability. X-ray powder diffraction (SR-μ-XRPD) in transmission geometry allowed visualization of the distributions of calcium carbonate and oxalates along the sample depths. In a second step, X-ray fluorescence (SR-μ-XRF) was used to check the efficiency/integrity of the protective surface coating layer. This was done by measuring the sulfur distribution on the stone surface after exposing the protected stones to sulfuric acid. XRPD showed the formation of a protective oxalate layer with a thickness of 5–15 µm on the less porous stone, while a 20–30 µm thick layer formed on the more porous stone. The XRF study showed that the optimal treatment time depends on the stone porosity. Increasing the treatment time from 1 to 3 h resulted in a decreased efficiency of the protective layer for the low porosity stone. We assume that this is due to the formation of vertical channels (cracks) in the protective layer.

MRS Advances ◽  
2020 ◽  
Vol 5 (62) ◽  
pp. 3273-3282
Author(s):  
I. Cosme-Torres ◽  
M.G. Macedo-Miranda ◽  
S.M. Martinez-Gallegos ◽  
J.C. González-Juárez ◽  
G. Roa-Morales ◽  
...  

AbstractThe heterogeneous catalyst HTCMgFe was used in the degradation of the IC, through the heterogeneous photo-fenton treatment, this material in combination with H2O2 and UV light degraded the dye in 30 min at pH 3. As the amount of HTCMgFe increases the degradation it was accelerated because there are more active catalytic sites of Fe2+ on the surface of the material, which generates a greater amount of •OH radicals. The HTCMgFe was characterized by infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and X-ray energy dispersive elemental analysis (EDS). The UV-vis spectrum shows that the absorption bands belonging to the chromophore group of the IC disappear as the treatment time passes, indicating the degradation of the dye.


2021 ◽  
Vol 16 ◽  
pp. 155892502199275
Author(s):  
Ajinkya Powar ◽  
Anne Perwuelz ◽  
Nemeshwaree Behary ◽  
Le vinh Hoang ◽  
Thierry Aussenac ◽  
...  

Color stripping is one of the most convenient ways to rectify the various shade faults occurred during printing or dyeing process of textiles. But, the conventional chemical assisted process poses serious risk of the environmental pollution. Secondly, the chemical recycling of the cellulosic fibers may be disrupted due to the presence of the impurities like colorants, finishes, and the additives in the discarded textiles. So, there is a need to study ways to remove such impurities from the discarded cellulosic textiles in a sustainable manner. This work examines the decolorization of the pigment prints on cellulosic fabrics at pilot scale using an ozone-assisted process. The effect of varying pH, ozone concentration and the treatment time on the decolorization of the pigment prints was optimized using the response surface methodology technique. The effects of ozonation process parameters on the mechanical properties of cellulosic cotton fabric were measured. Decolorization of pigment printed samples was studied with respect to the surface effects by a scanning electron microscopy (SEM), and the chemical removal effects of ozonation treatment were studied using X-ray photoelectron spectroscopy. The possible mechanism regarding the action of ozone for the decolorization is discussed.


1999 ◽  
Vol 79 (1) ◽  
pp. 103-109 ◽  
Author(s):  
F. Courchesne ◽  
J.-F. Laberge ◽  
A. Dufresne

The role of soil organic matter (OM) on SO4 retention was investigated by comparing OM content, SO4 retention, and the distribution of Fe, Al and Si compounds in OM-poor (Grands-Jardins, PGJ) and OM-rich (Hermine, HER) Podzols from Québec, Canada. At both sites, four pedons were sampled by horizon; soil pH in H2O, organic C, phosphate-extractable SO4 and, sodium pyrophosphate, acid ammonium oxalate and dithionite-citrate-bicarbonate (DCB) extractable Fe, Al and Si were measured for each mineral horizon. The mineralogy of the clay (<2 µm) and fine silt (2–20 µm) fractions of selected horizons was determined by X-ray diffraction (XRD) and infrared spectroscopy (IR). Weighted mean organic C and pyrophosphate extractable Fe and Al contents were significantly higher in the HER than in the PGJ sola, while the PGJ soils were richer in amorphous inorganic Al. No trends were observed for inorganic Fe compounds. Chemical dissolution and IR allowed the identification of short-range ordered aluminosilicates, probably allophane, in the OM-poor and slightly acidic to neutral PGJ soils. These materials were absent from the OM-rich and acidic HER soils. Phosphate extractions showed that the weighted mean native SO4 content was five times higher in the PGJ than in the HER soil. Finally, native SO4 was strongly related to inorganic Fe, Al and Si (associated with allophane) at PGJ but only to inorganic Fe at HER. These results indicate that OM indirectly affects SO4 sorption through the influence organic substances exerts on the nature and distribution of pedogenic Fe, Al and Si compounds, such as allophane, in Podzolic profiles. Key words: Organic matter, sulfate, imogolite, allophane, silica, Podzol


2012 ◽  
Vol 45 (5) ◽  
pp. 906-913 ◽  
Author(s):  
Herve Palancher ◽  
Anne Bonnin ◽  
Veijo Honkimäki ◽  
Heikki Suhonen ◽  
Peter Cloetens ◽  
...  

This article describes a single-shot methodology to derive an average coating thickness in multi-particle core–shell systems exhibiting high X-ray absorption. Powder composed of U–Mo alloy particles surrounded by a micrometre-thick UO2protective layer has been used as a test sample. Combining high-energy X-ray diffraction and laser granulometry, the average shell thickness could be accurately characterized. These results have been validated by additional measurements on single particles by two techniques: X-ray nanotomography and high-energy X-ray diffraction. The presented single-shot approach gives rise to many potential applications on core–shell systems and in particular on as-fabricated heterogeneous nuclear fuels.


2014 ◽  
Vol 809-810 ◽  
pp. 43-52
Author(s):  
Hua Hua Wang ◽  
Nan Li ◽  
Kai Li ◽  
Yuan Bu ◽  
Wen Le Dai ◽  
...  

Multiwalled carbon nanotubes (MWCNTs) as an excellent supporter covered with a thick layer of cobalt phthalocyanine (CoPc) were prepared by in-situ synthesis. Platinum particles were adopted to enhance the conductivity of CoPc-MWCNTs. The final nanocomposite Pt-CoPc-MWCNTs was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM). Strong aromatic π-π stacking between MWCNTs and CoPc made CoPc in-situ forming on MWCNTs. With homogeneous thickness of CoPc covered on the MWCNTs and Pt particles equally distributed, the nanocomposite was used as electrocatalyst. The electrochemical properties of the composite got researched by casting the dispersion of Pt-CoPc-MWCNTs on the glassy carbon electrode. Compared with other modified electrodes, Pt-CoPc-MWCNTs/GC electrode exhibited excellent electrochemical activity towards dopamine (DA) and uric acid (UA). Linear responses for DA and UA were obtained in the ranges of 5 to 170 μM and 5 to 100 μM, and limits of detection were 2.6 and 1.4 μM (S/N= 3), respectively. Simultaneous detection of DA and UA in the presence of ascorbic acid (AA) also displayed selective property, with no interference to each other.


Author(s):  
Rafael Cipriano da Silva ◽  
Edilene Pereira Ferreira ◽  
Antonio Carlos de Azevedo

Abstract The objective of this work was to analyze the mineralogical, morphological, and compositional modifications resulting from the weathering of diabase grains buried into soil under different land uses for up to 378 days. Samples of comminuted diabase were put into polyester bags and buried into soil under corn crop, elephant grass, and woods, being unburied and evaluated after four time periods. The samples of the remineralizer (RM) were analyzed by X-ray diffractometry, total chemical analysis, scanning electron microscopy, and Al (Ald and Alo) and Fe (Fed and Feo) contents extracted by sodium dithionite-citrate-bicarbonate (DCB) and ammonium oxalate (AAO) solutions. Plagioclases and pyroxenes were the most weathered minerals in all three land uses and showed the same pattern of elemental gains and losses. The characterization of Fe and Al solubility in DCB and AAO showed that the greatest change in these elements was from the lithogenic and crystalline to the pedogenic and amorphous phase, when compared with their total content. Plagioclases and pyroxenes were the most weathered minerals, and Fe and Al show a great transfer from the crystalline to the amorphous phase, with values up to 26 and 175, respectively, for the ratios between bags with RM/Feo and RM-control and bags with RM/Alo and RM-control.


2021 ◽  
Vol 22 (48) ◽  
Author(s):  
Tran Thi Bich Quyen ◽  
Ngo Nguyen Tra My ◽  
Do Thi Thuy Ngan ◽  
Duy Toan Pham ◽  
Doan Van Hong Thien

For the first time, cuprous oxide nanocubes (Cu2O NCBs) were successfully combined with chitosan nanoparticles (CS NPs) to generate Cu2O NCBs/CS NPs composites material with highly optical property and photocatalytic activity using a simple and eco-friendly synthetic approach at room temperature for 30 min. The synthesized Cu2O NCBs NPs/CS NPs were determined characterizations by Ultraviolet-visible spectroscopy (UV-vis), Fourier transform infrared spectroscopy (FTIR), X – ray Diffraction (XRD),  Transmission Electron Microscope (TEM) and Energy-dispersive X-ray spectroscopy (EDX). Results show that the Cu2O NCBs/CS NPs composites have an average particle size of ~3-5 nm; in which, Cu2O has the form of nanocubes (Cu2O NCBs) with size ~3-4 nm and chitosan nanoparticles with spherical shape (CS NPs) with size ~4-5 nm. In addition, the percent (%) composition of elements present in Cu2O NCBs/CS NPs composites material have been obtained respective: Cu (23.99%), O (38.18%), and C (33.61%). Moreover, Cu2O NCBs/CS NPs composites material was also investigated for photocatalytic activity applied in p-nitrophenol degradation. The obtained results showed that the catalytic capability of Cu2O NCBs/CS NPs for p-nitrophenol reduction reached the highest efficiency >55% in the treatment time of 25 min, and this efficiency was higher than that result of using ZnO@chitosan nanoparticles (ZnO@CS NPs) catalyst under the same conditions for comparison.


1972 ◽  
Vol 9 (1) ◽  
pp. 117-119 ◽  
Author(s):  
Dwight A. Sangrey

A unique characteristic of many naturally cemented sensitive soils is that they are made up of finely ground fresh rock debris, "rock flour", much of which is very susceptable to chemical weathering or decomposition. Many of these minerals can be identified by X-ray diffraction. The decomposition of these minerals produces secondary products which can act as effective natural cements. A process is outlined whereby the sequence of deposition, weathering and cementation can account for the observed mechanical behaviour of naturally cemented soils.


2021 ◽  
Vol 16 (1) ◽  
pp. 199-210
Author(s):  
Máté Karlik ◽  
◽  
Ildikó GYOLLAI ◽  
Anna VANCSIK ◽  
Krisztián FINTOR ◽  
...  

The catchment (bedrock and soil) and sediments of lake Bolătău, Romania were studied by high resolution multi-methodological investigations to characterize paleoenvironmental and formation conditions. Particle size analyses, optical and cathodoluminescence microscopy, FTIR-ATR and Raman spectroscopy, X-ray powder diffraction, and XRF were applied for microtextural, chemical, micro-mineralogical and embedded organic material characterization and distribution of the sediments, especially concerning geochemical conditions, like pH and redox potential change. Our results support physical and chemical weathering in the process of soil formation with appearance of the new minerals appear (10Å sized phyllosilicates and clay minerals). Comparison of these studies offer possible differentiation of syn- and diagenetic mineralization, the clarification of debris contribution, microbial mediation and complex mineralization via decomposition of cell and extracellular polymeric substance. Based on the analyses on the abrasives, a suboxic environment prevailed in the depositional area and considerable microbial contribution is proposed via accumulation of lake sediments.


Author(s):  
S. Gawor ◽  
J. B. Wiskel ◽  
D. G. Ivey ◽  
J. Liu ◽  
H. Henein

Abstract A standard NACE hydrogen induced crack test was used to evaluate the resistance of two compositions of X70 steel (X70-X (Ca/S ratio of 2.5) and X70-B (Ca/S ratio of &lt; 0.5)) under severe (pH = 2.7 and 100% H2S) and mild (pH = 5.5 and 100% H2S) sour service conditions. An ultrasonic technique was developed to quantify the severity of hydrogen cracking in both steels as a function of test conditions, steel type and time. In this procedure, a series of local ultrasonic measurements was taken for each test sample to determine a local crack to backwall signal ratio (LCBR). The LCBR values were integrated over the entire sample to give a global crack to backwall ratio (GCBR). A larger GCBR value corresponds to greater hydrogen cracking severity in the sample. Energy dispersive X-ray (EDX) spectroscopy and glancing angle X-ray diffraction (XRD) were used to characterize the surface corrosion products that formed during testing. For severe sour service conditions, the GCBR value reached an asymptotic value of approximately 33% and 47% for X70-X (after 4 days) and X70-B (after 2 days) steels, respectively. For mild sour service conditions, no cracking was observed for testing of less than 16 days. After 32 days, X70-B showed a GCBR of approximately 18%. The onset of cracking of X70-X steel occurred between 32 and 64 days. Samples tested for 64 days showed a GCBR of 30% and 16% for X70-X and X70-B, respectively. Glancing XRD measurements showed the presence of surface FeS on both steels tested under mild sour service. Quantitative XRD (QXRD) analysis was used to obtain the surface coverage of FeS as a function of test time. EDX mapping confirmed the presence of a high sulfur content over a significant fraction of the surface. XRD measurements of X70-B steel under severe sour service after 8 days did not show a significant amount of FeS. The surface FeS is believed to alter hydrogen ingress into the steel, making it difficult to directly compare measured GCBR values obtained under mild and severe sour service.


Sign in / Sign up

Export Citation Format

Share Document