scholarly journals Effects of Silk-worm Excrement Biochar Combined with Different Iron-Based Materials on the Speciation of Cadmium and Lead in Soil

2018 ◽  
Vol 8 (10) ◽  
pp. 1999 ◽  
Author(s):  
Pengyang Bian ◽  
Jingjing Zhang ◽  
Chaolan Zhang ◽  
He Huang ◽  
Qun Rong ◽  
...  

A 56d incubation experiment was conducted to explore the effects of the silk-worm excrement biochar (500 °C, BC) combined with different iron-based materials (FeCl3, FeSO4, and reduced iron powder) on the speciation of cadmium (Cd) and lead (Pb) in a contaminated soil. Application rate of BC and iron-based materials is 1% (W/W) and 0.2% (W/W) of the soil, respectively. At the same time, the soil physicochemical properties, such as pH, cation exchange capacity (CEC), and the structure of soil, were determined in order to explore the influence mechanism of amendments to forms of Cd and Pb in soil. The results show that the stabilization effects on Cd is (BC + FeSO4) > (BC + FeCl3) > (BC + Fe) > (BC) and Pb is (BC + Fe) > (BC + FeSO4) > (BC + FeCl3) > (BC) at the end of incubation, compared with the effect of the control group. The treatment of (BC + FeSO4) is the most effective in terms of the stabilization of Cd and Pb, which makes the percentages of organic-bound and residual Cd and Pb increase by 40.90% and 23.51% respectively. In addition, with different ways of treatment, the pH value and CEC of soil see a remarkable increase by 1.65–2.01 units and 2.01–2.58 cmol·kg−1 respectively. X-ray diffraction (XRD) patterns show that the soil imprisons Cd and Pb in different mineral phases. As such the treatment of (BC + FeSO4) can significantly improve soil environment, increase soil pH value & CEC and exert a relatively good stabilization effect on both Cd and Pb.

Clay Minerals ◽  
2012 ◽  
Vol 47 (3) ◽  
pp. 355-364 ◽  
Author(s):  
S. Fukuchi ◽  
M. Fukushima ◽  
R. Nishimoto ◽  
G. Qi ◽  
T. Sato

AbstractTo enhance the catalytic activities of zeolites for the polycondensation reactions of humic precursors, Fe was loaded into a zeolite via an ion-exchange reaction and the resulting product was subjected to calcination at 773 K. Two types iron-loaded zeolites were prepared using one equivalent (Fe-Z-1) and 10-equivalents (Fe-Z-10) of Fe2+ to the cation-exchange capacity of a natural zeolite from Niki town (Hokkaido, Japan). X-ray diffraction (XRD) patterns and X-ray photoelectron spectroscopy (XPS) spectra showed that the Fe(II) that was originally loaded into the cation-exchange sites in the zeolite became oxidized to a Fe(III) ionic species during the preparation. The catalytic activities of each zeolite were evaluated, based on the degree of darkening for reaction mixtures containing catechol, glycine and glucose as model humic precursors. The catalytic activities of Fe-Z-1 and Fe-Z-10 were higher than that for an untreated zeolite, and increased with the amount of Fe in the zeolite.


2021 ◽  
Vol 37 (4) ◽  
pp. 791-796
Author(s):  
Ho Soon Min ◽  
Ng Sha Shiong

The successive ionic layer adsorption and reaction method or called SILAR method was used to produce cobalt selenide thin films for the first time. The deposition was carried out onto the substrate under different various pH values. The X-ray diffraction (XRD), field emission scanning electron microscope (FESEM) and ultraviolet visible spectrophotometer were used to investigate the structure, morphology and optical properties of thin films, respectively. The XRD patterns confirmed that the presence of cubic phase cobalt selenide thin films. The grain size increased with increasing the pH value from pH 2 to pH 4 based on the FESEM images. The band gap values are in the range of 2 eV to 2.5 eV.


Clay Minerals ◽  
2016 ◽  
Vol 51 (3) ◽  
pp. 325-350 ◽  
Author(s):  
Stephen Hillier ◽  
Rik Brydson ◽  
Evelyne Delbos ◽  
Tony Fraser ◽  
Nia Gray ◽  
...  

AbstractTwenty one samples of relatively pure tubular halloysites (HNTs) from localities in Australia, China, New Zealand, Scotland, Turkey and the USA have been investigated by X-ray diffraction (XRD), infrared spectroscopy (IR) and electron microscopy. The halloysites occur in cylindrical tubular forms with circular or elliptical cross sections and curved layers and also as prismatic tubular forms with polygonal cross sections and flat faces. Measurements of particle size indicate a range from 40 to 12,700 nm for tube lengths and from 20 to 600 nm for diameters. Size distributions are positively skewed with mean lengths ranging from 170 to 950 nm and mean diameters from 50 to 160 nm. Cylindrical tubes are systematically smaller than prismatic ones. Features related to order/ disorder in XRD patternse.g.as measured by a ‘cylindrical/prismatic’ (CP) index and IR spectra as measured by an ‘OH-stretching band ratio’ are related to the proportions of cylindricalvs. prismatic tubes and correlated with other physical measurements such as specific surface area and cation exchange capacity. The relationships of size to geometric form, along with evidence for the existence of the prismatic form in the hydrated state and the same 2M1stacking sequence irrespective of hydration state (i.e.10vs. 7 Å) or form, suggests that prismatic halloysites are the result of continued growth of cylindrical forms.


2015 ◽  
Vol 7 (1) ◽  
pp. 1346-1351
Author(s):  
Ch.Gopal Reddy ◽  
Ch. Venkateshwarlu ◽  
P. Vijaya Bhasker Reddy

Co-Zr substituted M-type hexagonal barium ferrites, with chemical formula BaCoxZrxFe12-2xO19 (where x = 0.0, 0.2, 0.4, 0.6, 0.8 and 1.0), have been synthesized by double sintering ceramic method. The crystallographic properties, grain morphology and magnetic properties of these ferrites have been investigated by X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM) and Vibrating Sample Magnetometer (VSM). The XRD patterns confirm the single phase with hexagonal structure of prepared ferrites. The magnetic properties have been investigated as a function of Co and Zr ion composition at an applied field in the range of 20 KOe. These studies indicate that the saturation magnetization (Ms) in the samples increases initially up to the Co-Zr composition of x=0.6 and decreases thereafter. On the other hand, the coercivity (Hc) and Remanent magnetization (Mr) are found to decrease continuously with increasing Co-Zr content. This property is most useful in permanent magnetic recording. The observed results are explained on the basis of site occupation of Co and Zr ions in the samples.


1994 ◽  
Vol 59 (6) ◽  
pp. 1311-1318 ◽  
Author(s):  
Ladislav Svoboda ◽  
Petr Vořechovský

The properties of cellulose chelating ion exchangers Ostsorb have been studied in the sorption of cadmium and lead from aqueous solutions. The Cd(II) and Pb(II) ions are trapped by the Ostsorb OXIN and Ostsorb DETA ion exchangers most effectively in neutral and alkaline media but at these conditions formation of stable hydrolytic products of both metals competes with the exchange equilibria. From this point of view, Ostsorb DTTA appears to be a more suitable sorbent since it traps the Pb(II) and Cd(II) ions in acidic media already. Chloride ions interfere with the sorption of the two metals by Ostsorb DTTA whereas the ionic strength adjusted by the addition of sodium perchlorate does not affect the exchange capacity of this ion exchanger.


2020 ◽  
Vol 66 (No. 9) ◽  
pp. 468-476
Author(s):  
Miroslav Jursík ◽  
Martin Kočárek ◽  
Michaela Kolářová ◽  
Lukáš Tichý

Six sunflower herbicides were tested at two application rates (1N and 2N) on three locations (with different soil types) within three years (2015–2017). Efficacy of the tested herbicides on Chenopodium album increased with an increasing cation exchange capacity (CEC) of the soil. Efficacy of pendimethalin was 95%, flurochloridone and aclonifen 94%, dimethenamid-P 72%, pethoxamid 49% and S-metolachlor 47%. All tested herbicides injured sunflower on sandy soil (Regosol) which had the lowest CEC, especially in wet conditions (phytotoxicity 27% after 1N application rate). The highest phytotoxicity was recorded after the application of dimethenamid-P (19% at 1N and 45% at 2N application rate). Main symptoms of phytotoxicity were leaf deformations and necroses and the damage of growing tips, which led to destruction of some plants. Aclonifen, pethoxamid and S-metolachlor at 1N did not injure sunflower on the soil with the highest CEC (Chernozem) in any of the experimental years. Persistence of tested herbicides was significantly longer in Fluvisol (medium CEC) compared to Regosol and Chernozem. Dimethenamid-P showed the shortest persistence in Regosol and Chernozem. The majority of herbicides was detected in the soil layer 0–5 cm in all tested soils. Vertical transport of herbicides in soil was affected by the herbicide used, soil type and weather conditions. The highest vertical transport was recorded for dimethenamid-P and pethoxamid (4, resp. 6% of applied rate) in Regosol in the growing season with high precipitation.  


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Eduardo da Rosa Vieira ◽  
Luciano Volcanoglo Biehl ◽  
Jorge Luis Braz Medeiros ◽  
Vagner Machado Costa ◽  
Rodrigo Jorge Macedo

AbstractQuench hardening aims at the microstructural transformation of steels in order to improve hardness and mechanical strength. The aim phase is, in most cases, the martensite. It is necessary to heat the material until it obtains its austenitization and quenching by immersion in a fluid. Currently, it is common to use watery polymeric solutions in this procedure. These fluids, which are the mixture of polymers in water, vary their thermal exchange capacity depending on the concentrations applied. The increase in concentration minimizes the removal of heat from the part, reducing the formation capacity of martensite, and developing a lower hardness and strong steel. In this work, microstructural characteristics and properties of AISI 1045 steel quenched in solutions based on polyvinylpyrrolidone (PVP) in 10, 15, 20, and 25% concentration were evaluated. The microstructural characterization quantified the percentage of the phases in each concentration, demonstrating a reduction of martensite as the concentrations were high. The investigation of the samples by x-ray diffraction confirmed the absence of austenite retained in the material. Furthermore, a microhardness scale between the core and the surface was constructed, in which a reduction gradient of the indices of this property towards the core of the sample was evidenced.


Materials ◽  
2021 ◽  
Vol 14 (10) ◽  
pp. 2518
Author(s):  
Dorota Kołodyńska ◽  
Yongming Ju ◽  
Małgorzata Franus ◽  
Wojciech Franus

The possibility of application of chitosan-modified zeolite as sorbent for Cu(II), Zn(II), Mn(II), and Fe(III) ions and their mixtures in the presence of N-(1,2-dicarboxyethyl)-D,L-aspartic acid, IDHA) under different experimental conditions were investigated. Chitosan-modified zeolite belongs to the group of biodegradable complexing agents used in fertilizer production. NaP1CS as a carrier forms a barrier to the spontaneous release of the fertilizer into soil. The obtained materials were characterized by Fourier transform infrared spectroscopy (FTIR); surface area determination (ASAP); scanning electron microscopy (SEM-EDS); X-ray fluorescence (XRF); X-ray diffraction (XRD); and carbon, hydrogen, and nitrogen (CHN), as well as thermogravimetric (TGA) methods. The concentrations of Cu(II), Zn(II), Mn(II), and Fe(III) complexes with IDHA varied from 5–20 mg/dm3 for Cu(II), 10–40 mg/dm3 for Fe(III), 20–80 mg/dm3 for Mn(II), and 10–40 mg/dm3 for Zn(II), respectively; pH value (3–6), time (1–120 min), and temperature (293–333 K) on the sorption efficiency were tested. The Langmuir, Freundlich, Dubinin–Radushkevich, and Temkin adsorption models were applied to describe experimental data. The pH 5 proved to be appropriate for adsorption. The pseudo-second order and Langmuir models were consistent with the experimental data. The thermodynamic parameters indicate that adsorption is spontaneous and endothermic. The highest desorption percentage was achieved using the HCl solution, therefore, proving that method can be used to design slow-release fertilizers.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Bernd Wegener ◽  
Maik Behnke ◽  
Stefan Milz ◽  
Volkmar Jansson ◽  
Christian Redlich ◽  
...  

AbstractDespite the high potential of healthy bone to regenerate, the reconstruction of large bone defects remains a challenge. Due to the lack of mechanical stability of existing bone substitutes, recently developed degradable metallic alloys are an interesting alternative providing higher load-bearing capabilities. Degradable iron-based alloys therefore might be an attractive innovation. To test the suitability of a newly-designed iron-based alloy for such applications, an animal experiment was performed. Porous iron-based degradable implants with two different densities and a control group were tested. The implants were positioned in the proximal tibia of Merino sheep. Over a period of 6 and 12 months, blood and histological parameters were monitored for signs of inflammation and degradation. In the histological evaluation of the implants` environment we found degraded alloy particles, but no inflammatory reaction. Iron particles were also found within the popliteal lymph nodes on both sides. The serum blood levels of phosphorus, iron and ferritin in the long term groups were elevated. Other parameters did not show any changes. Iron-based degradable porous bone replacement implants showed a good biocompatibility in this experiment. For a clinical application, however, the rate of degradation would have to be significantly increased. Biocompatibility would then have to be re-evaluated.


2020 ◽  
Vol 10 (03) ◽  
pp. 2050003
Author(s):  
M. R. Hassan ◽  
M. T. Islam ◽  
M. N. I. Khan

In this research, influence of adding Li2CO3 (at 0%, 2%, 4%, 6%) on electrical and magnetic properties of [Formula: see text][Formula: see text]Fe2O4 (with 60% Ni and 40% Mg) ferrite has been studied. The samples are prepared by solid state reaction method and sintered at 1300∘C for 6[Formula: see text]h. X-ray diffraction (XRD) patterns show the samples belong to single-phase cubic structure without any impurity phase. The magnetic properties (saturation magnetization and coercivity) of the samples have been investigated by VSM and found that the higher concentration of Li2CO3 reduces the hysteresis loss. DC resistivity increases with Li2CO3 contents whereas it decreases initially and then becomes constant at lower value with temperature which indicates that the studied samples are semiconductor. The dielectric dispersion occurs at a low-frequency regime and the loss peaks are formed in a higher frequency regime, which are due to the presence of resonance between applied frequency and hopping frequency of charge carriers. Notably, the loss peaks are shifted to the lower frequency with Li2CO3 additions.


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