Leaching Behavior of Fixed-Bed Gasification Ash Derived from North Dakota Lignite

1985 ◽  
Vol 65 ◽  
Author(s):  
D. J. Hassett ◽  
K. R. Henke ◽  
G. J. McCarthy

ABSTRACTthree different fixed-bed gasifiers have been leached using: (1) the EPA-EP leaching test; (2) a similar test that starts with a synthetic North Dakota groundwater; (3) the ASTM D3987–81 method; (4) a long-term (120 day) leaching experiment. The gasification ashes were highly alkaline and produced pH's in the range 10–13 during tests 2 through 4. Compositions of major, minor and trace elements were determined by AAS and ICAP analyses of leachates. None of the EPA-EP test leachates from any of the ashes exceeded the EP Trigger values that define a hazardous waste according to the RCRA criteria. The long-term leaching experiments provided insights into the rates of extraction of elements from ash and could be useful in modeling selected failure scenarios in an ash disposal pit. At various times during the long-term leaching experiments, substantial fractions of the Na, K, Al, S, As, Mo, Se and V in the ash were extracted. Liquid to solid (l:s) ratios were important in determining the quantities of elements extracted and in controlling solution pH; during most of the 120 day experiments, pH's were near 13 in a 2:1 ratio experiment and just below 10 in a 20:1 ratio experiment. X-ray diffraction analysis of the leaching residue indicated that only a portion of the ash reacted with the leaching solutions. The reaction products were largely noncrystalline, but minor amounts of zeolites, calcite and gibbsite were identified. The formation of such secondary solid phases appears to be important in controlling leachant concentrations.

2012 ◽  
Vol 15 (3) ◽  
pp. 157-163 ◽  
Author(s):  
J.L. Contreras ◽  
M.A. Ortiz ◽  
G.A. Fuentes ◽  
M. Ortega ◽  
R. Luna ◽  
...  

The effect of WOx over Ni-hydrotalcite catalysts to produce H2 by ethanol steam reforming was studied. The catalysts were characterized by N2 physisorption (BET area), X-ray diffraction, Infrared and UV-vis spectroscopies. The W concentration ranged from 0.5 to 3 wt%. As W concentration increased, the intensity of XRD reflections of the Ni catalysts decreased. The porous structure of the materials consisted of parallel layers with a monomodal mesoporous distribution. The surface groups detected by IR were: -OH, Al-OH, Mg-OH, W=O and CO32-. UV-vis results suggested that Ni2+ ions were substituted by W ions. The catalytic evaluations were made in a fixed bed reactor using a water/ethanol mol ratio of 4 at 450°C. Catalysts with low loadings of W (0.5 and 1%) showed the highest H2 production and stability. W promoted the conversion of ethanol towards hydrogen in the case of the Ni-hydrotalcite catalysts. The reaction products were; H2, CO2, CH3CHO, CH4 and C2H4. The catalysts did not produce CO.


1985 ◽  
Vol 65 ◽  
Author(s):  
Robert J. Stevenson ◽  
Gregory J. McCarthy

ABSTRACTThe mineralogy of nine ash samples derived from North Dakota lignite and gasified in three different fixed-bed producers was determined by x-ray diffraction (XRD) and scanning electron microscopy (SEM). The gasifiers had maximum temperatures in the 1100–1250°C range, but included several differences in ash residence time, oxidizing gas and pressure, and ash handling conditions. The lignite gasified came from the same geologic formation, but the mines were separated by 20 km. Despite these differences, all of the ash specimens had the same basic mineralogy: glass at the 15–30 wt.% level; a crystalline phase assemblage of ortho- and pyro-silicates (merwinite, dicalcium silicate (C2S), C2S-like phases, and melilite), network aluminosilicates (nepheline, carnegieite, and a sodalite-structure phase), oxides (ferrite spinel, hematite, and periclase), and calcite along with residual lignite minerals (quartz and felspar). SEM morphologies and XRD comparisons of the amounts of crystalline phases in size fractions both indicated that some of the phases (particularly merwinite and carnegieite) crystallized during cooling of portions of the ash that had melted during gasification.


Nanomaterials ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1892
Author(s):  
Tan Wang ◽  
Cong Wang ◽  
Xianbao Xu ◽  
Zhen Li ◽  
Daoliang Li

In this paper, a new nanocomposite AuNPs/MXene/ERGO was prepared for sensitive electrochemical detection of nitrite. The nanocomposite was prepared by a facile one-step electrodeposition, HAuCl4, GO and MXene mixed in PBS solution with the applied potential of –1.4 V for 600 s. The modified material was characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD) and cyclic voltammetry (CV). The electrochemical behavior of nitrite at the modified electrode was performed by CV and chronoamperometry. The AuNPs/MXene/ERGO/GCE showed a well-defined oxidation peak for nitrite at +0.83 V (Vs. Ag/AgCl) in 0.1 M phosphate buffer solution (pH 7). The amperometric responses indicated the sensor had linear ranges of 0.5 to 80 μM and 80 to 780 μM with the LOD (0.15 μM and 0.015 μM) and sensitivity (340.14 and 977.89 μA mM–1 cm–2), respectively. Moreover, the fabricated sensor also showed good selectivity, repeatability, and long-term stability with satisfactory recoveries for a real sample. We also propose the work that needs to be done in the future for material improvements in the conclusion.


2020 ◽  
Vol 9 (1) ◽  
pp. 998-1008
Author(s):  
Guo Li ◽  
Zheng Zhuang ◽  
Yajun Lv ◽  
Kejin Wang ◽  
David Hui

AbstractThree nano-CaCO3 (NC) replacement levels of 1, 2, and 3% (by weight of cement) were utilized in autoclaved concrete. The accelerated carbonation depth and Coulomb electric fluxes of the hardened concrete were tested periodically at the ages of 28, 90, 180, and 300 days. In addition, X-ray diffraction, thermogravimetry, and mercury intrusion porosimetry were also performed to study changes in the hydration products of cement and microscopic pore structure of concrete under autoclave curing. Results indicated that a suitable level of NC replacement exerts filling and accelerating effects, promotes the generation of cement hydration products, reduces porosity, and refines the micropores of autoclaved concrete. These effects substantially enhanced the carbonation and chloride resistance of the autoclaved concrete and endowed the material with resistances approaching or exceeding that of standard cured concrete. Among the three NC replacement ratios, the 3% NC replacement was the optimal dosage for improving the long-term carbonation and chloride resistance of concrete.


MRS Advances ◽  
2016 ◽  
Vol 1 (22) ◽  
pp. 1631-1636 ◽  
Author(s):  
Boya Cui ◽  
D. Bruce Buchholz ◽  
Li Zeng ◽  
Michael Bedzyk ◽  
Robert P. H. Chang ◽  
...  

ABSTRACTThe cross-plane thermal conductivities of InGaZnO (IGZO) thin films in different morphologies were measured on three occasions within 19 months, using the 3ω method at room temperature 300 K. Amorphous (a-), semi-crystalline (semi-c-) and crystalline (c-) IGZO films were grown by pulsed laser deposition (PLD), followed by X-ray diffraction (XRD) for evaluation of film quality and crystallinity. Semi-c-IGZO shows the highest thermal conductivity, even higher than the most ordered crystal-like phase. After being stored in dry low-oxygen environment for months, a drastic decrease of semi-c-IGZO thermal conductivity was observed, while the thermal conductivity slightly reduced in c-IGZO and remained unchanged in a-IGZO. This change in thermal conductivity with storage time can be attributed to film structural relaxation and vacancy diffusion to grain boundaries.


Minerals ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 626 ◽  
Author(s):  
Salah ◽  
Gaber ◽  
Kandil

The sorption of uranium and thorium from their aqueous solutions by using 8-hydroxyquinoline modified Na-bentonite (HQ-bentonite) was investigated by the batch technique. Na-bentonite and HQ-bentonite were characterized by X-ray fluorescence (XRF), X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier Transform Infrared (FTIR) spectroscopy. Factors that influence the sorption of uranium and thorium onto HQ-bentonite such as solution pH, contact time, initial metal ions concentration, HQ-bentonite mass, and temperature were tested. Sorption experiments were expressed by Freundlich and Langmuir isotherms and the sorption results demonstrated that the sorption of uranium and thorium onto HQ-bentonite correlated better with the Langmuir isotherm than the Freundlich isotherm. Kinetics studies showed that the sorption followed the pseudo-second-order kinetic model. Thermodynamic parameters such as ΔH°, ΔS°, and ΔG° indicated that the sorption of uranium and thorium onto HQ-bentonite was endothermic, feasible, spontaneous, and physical in nature. The maximum adsorption capacities of HQ-bentonite were calculated from the Langmuir isotherm at 303 K and were found to be 63.90 and 65.44 for U(VI) and Th(IV) metal ions, respectively.


Nanomaterials ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 1309 ◽  
Author(s):  
Karla Čech Barabaszová ◽  
Sylva Holešová ◽  
Kateřina Šulcová ◽  
Marianna Hundáková ◽  
Barbora Thomasová

Microbial infection and biofilm formation are both problems associated with medical implants and devices. In recent years, hybrid organic-inorganic nanocomposites based on clay minerals have attracted significant attention due to their application potential in the field of antimicrobial materials. Organic drug/metal oxide hybrids exhibit improved antimicrobial activity, and intercalating the above materials into the interlayer of clay endows a long-term and controlled-release behavior. Since antimicrobial activity is strongly related to the structure of the material, ultrasonic treatment appears to be a suitable method for the synthesis of these materials as it can well control particle size distribution and morphology. This study aims to prepare novel, structurally stable, and highly antimicrobial nanocomposites based on zinc oxide/vermiculite/chlorhexidine. The influence of ultrasonic treatment at different time intervals and under different intercalation conditions (ultrasonic action in a breaker or in a Roset’s vessel) on the structure, morphology, and particle size of prepared hybrid nanocomposite materials was evaluated by the following methods: scanning electron microscopy, X-ray diffraction, energy dispersive X-ray fluorescence spectroscopy, carbon phase analysis, Fourier transforms infrared spectroscopy, specific surface area measurement, particle size analysis, and Zeta potential analysis. Particle size analyses confirmed that the ultrasonic method contributes to the reduction of particle size, and to their homogenization/arrangement. Further, X-ray diffraction analysis confirmed that ultrasound intercalation in a beaker helps to more efficiently intercalate chlorhexidine dihydrochloride (CH) into the vermiculite interlayer space, while a Roset’s vessel contributed to the attachment of the CH molecules to the vermiculite surface. The antibacterial activity of hybrid nanocomposite materials was investigated on Gram negative (Escherichia coli, Pseudomonas aeruginosa) and Gram positive (Staphylococcus aureus, Enterococcus faecalis) bacterial strains by finding the minimum inhibitory concentration. All hybrid nanocomposite materials prepared by ultrasound methods showed high antimicrobial activity after 30 min, with a long-lasting effect and without being affected by the concentration of the antibacterial components zinc oxide (ZnO) and CH. The benefits of the samples prepared by ultrasonic methods are the rapid onset of an antimicrobial effect and its long-term duration.


NANO ◽  
2019 ◽  
Vol 14 (11) ◽  
pp. 1950138 ◽  
Author(s):  
Sai Zhang ◽  
Shijun Yue ◽  
Jiajia Li ◽  
Jianbin Zheng ◽  
Guojie Gao

Au nanoparticles anchored on core–shell [Formula: see text]-Fe2O3@SnO2 nanospindles were successfully constructed through hydrothermal synthesis process and used for fabricating a novel nonenzymatic dopamine (DA) sensor. The structure and morphology of the Au/[Formula: see text]-Fe2O3@SnO2 trilaminar nanohybrid film were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM) and X-ray diffraction (XRD). The electrochemical properties of the sensor were investigated by cyclic voltammetry and amperometry. The experimental results suggest that the composites have excellent catalytic property toward DA with a wide linear range from 0.5[Formula: see text][Formula: see text]M to 0.47[Formula: see text]mM, a low detection limit of 0.17[Formula: see text][Formula: see text]M (S/[Formula: see text]) and high sensitivity of 397.1[Formula: see text][Formula: see text]A[Formula: see text]mM[Formula: see text][Formula: see text]cm[Formula: see text]. In addition, the sensor exhibits long-term stability, good reproducibility and anti-interference.


1979 ◽  
Vol 32 (9) ◽  
pp. 1931 ◽  
Author(s):  
H Becker ◽  
K Gustafsson ◽  
CL Raston ◽  
AH White

Single-crystal X-ray diffraction structure determinations are reported for three reaction products and photoisomers formed from reactions between an o-diphenoquinone valence isomer and primary and secondary amines, namely: 3,5-di-t-butyl-7-(3,5-di-t-butyl-2-hydroxyphenyl)-1-methyl-2,3-dihydro-1H-azepin-2-one (8; R1 = R2 = But, R3 = Me), its photochemical isomerization product 4,6-di-t-butyl-1-(3,5-di-t-butyl-2-hydroxyphenyl)-2-methyl-2-azabicyclo[3,2,0]hept-6-en-3-one (9; R1 = R2 = But, R3 = Me) and 4',5,7-tri-t-butyl-3'-(2,2-dimethylpropionyl)-1'-methylspiro[benzofuran-3(2H)-2'- pyrrolidinel-2,5'-dione (12; R1 = R2 = But, R3 = Me).


2012 ◽  
Vol 538-541 ◽  
pp. 166-171
Author(s):  
Wen Feng Ding ◽  
Yang Min Liang ◽  
Jian He ◽  
Li Tang ◽  
Jie Yu ◽  
...  

Cubic boron nitride (CBN) abrasive grains with surface titanium-deposited film were heat-treated during 550-950°C for 60 min under high vacuum circumstance. Detailed interfacial compounds analysis by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersion spectrometer (EDS), differential thermal analysis (DTA) indicates that the interfacial reactions are much dependent on the heating temperature to some extents, and the reaction products, TiN, TiB2 and TiB chiefly form the network structure. In particular, at 950°C the transition layers with excellent performance, CBN/TiB2/TiB/(TiB+TiN)/TiN/CBN, is realized.


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