Study on adsorption of Cr (VI) with natural zeolite modified by hydrotalcite

2013 ◽  
Author(s):  
Rongxiang Liu ◽  
Huanzhen Zhang
Keyword(s):  
Natural Zeolite

Microstructures and Properties of WC/Natural Zeolite Composites

2012 ◽  
Vol 27 (2) ◽  
pp. 129-133
Author(s):  
Yi-Fan ZHENG ◽  
Na ZHAO ◽  
Jie ZHANG ◽  
Xiao-Ye YU ◽  
Wei-Min MO
Keyword(s):  
Natural Zeolite

ION Exchange Characterisation of Modified Zeolite

1992 ◽  
Vol 26 (9-11) ◽  
pp. 2269-2272 ◽  
Author(s):  
Š Cerjan-Stefanovic ◽  
M. Kaštelan-Macan ◽  
T. Filipan
Keyword(s):  
Drinking Water ◽  
Ion Exchange ◽  
Anion Exchange ◽  
Natural Zeolite ◽  
Deionized Water ◽  
Isomorphous Substitution ◽  
Waste Waters ◽  
Modified Zeolite ◽  
Water Drinking

Isomorphous substitution of phosphorus into a natural zeolite affords the possibility to change the overall framework charge from negative to positive. The substances so created should be used for purification of waste waters. The work describes the preparation of phosphated zeolite, their characterisation and examples of their anion exchange of NO3 on observed in deionized water, drinking water and in the solution containing varying amounts of nitrate.

Life Time Improvement of Hierarchically Structured SAPO-34 Nanocatalyst in MTO Reaction via Applying Clinoptilolite, Investigating of Composite Design via RSM

2020 ◽  
Vol 23 ◽  
Author(s):  
Reza Yazdanpanah ◽  
Eshagh Moradiyan ◽  
Rouein Halladj ◽  
Sima Askari
Keyword(s):  
Surface Area ◽  
Natural Zeolite ◽  
Coke Formation ◽  
Life Time ◽  
Weight Percent ◽  
Light Olefins ◽  
Bet Surface Area ◽  
Relative Crystallinity ◽  
Mto Reaction ◽  
The Common

Aim and Objective: The research focuses on recent progress in the production of light olefins. Hence, the common catalyst of the reaction (SAPO-34) deactivates quickly because of coke formation, we reorganized the mechanism combining SAPO-34 with a natural zeolite in order to delay the deactivation time. Materials and Methods: The synthesis of nanocomposite catalyst was conducted hydrothermally using experimental design. Firstly, Clinoptilolite was modified using nitric acid in order to achieve nano scaled material. Then, the initial gel of the SAPO-34 was prepared using DEA, aluminum isopropoxide, phosphoric acid and TEOS as the organic template, sources of Aluminum, Phosphor, and Silicate, respectively. Finally, the modified zeolite was combined with SAPO-34's gel. Results: 20 different catalysts due to D-Optimal design were synthesized and the nanocomposite with 50 weight percent of SAPO-34, 4 hours Crystallization and early Clinoptilolite precipitation showed the highest relative crystallinity, partly high BET surface area and hierarchical structure. Conclusion: Different analysis illustrated the existence of both components. The most important property alteration of nanocomposite was the increment of pore mean diameters and reduction in pore volumes in comparison with free SAPO-34. Due to low price of Clinoptilolite, the new catalyst develops the economy of the process. Using this composite, according to formation of multi-sized pores located hierarchically on the surface of the catalyst and increased surface area, significant amounts of Ethylene and Propylene, in comparison with free SAPO-34, were produced, as well as deactivation time that was improved.

COPPER (Cu2+) REMOVAL FROM WATER USING NATURAL ZEOLITE FROM GEDANGSARI, GUNUNGKIDUL, YOGYAKARTA

2015 ◽  
Vol 2 (2) ◽  
Author(s):  
Wahyu Wilopo ◽  
Septiawan Nur Haryono ◽  
Doni Prakasa Eka Putra ◽  
I Wayan Warmada ◽  
Tsuyoshi Hirajima
Keyword(s):  
Waste Water ◽  
Economic Growth ◽  
Heavy Metals ◽  
Natural Zeolite ◽  
Adsorption Equilibrium ◽  
Waste Water Treatment ◽  
Batch Test ◽  
Maximum Capacity ◽  
Geological Materials ◽  
Langmuir Adsorption

Development of indusrialization and urbanization not only increase economic growth but also contribute to the environmental degradation, especially contamination of heavy metals in water. In other side, there are many geological materials have capability to immobilize heavy metals. Therefore, the objective of this research is to know the maximum capacity of natural zeolite from Trembono area, Gunung Kidul regency to immobilize copper (Cu2+) from water and to understand their mechanism. This experiment was carry out by a batch test. The result showed that the maximum capacity of zeolite to immobilize Cu (qmax) is 63,69 mmolCu/kg Zeolite according to Langmuir adsorption equilibrium model. In addition, the capability to immobilize Cu will increases due to decreasing the grain size. The result of this research can be used as an alternative for waste water treatment, especially Cu. Keywords: Removal, copper (Cu2+), natural zeolite, Langmuir isotherm

scholarly journals First Report on the Geologic Occurrence of Natural Na–A Zeolite and Associated Minerals in Cretaceous Mudstones of the Paja Formation of Vélez (Santander), Colombia

Crystals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 218
Author(s):  
Carlos Alberto Ríos-Reyes ◽  
German Alfonso Reyes-Mendoza ◽  
José Antonio Henao-Martínez ◽  
Craig Williams ◽  
Alan Dyer
Keyword(s):  
Natural Zeolite ◽  
Scanning Electron Micrographs ◽  
Total Sulfur ◽  
Zeolite A ◽  
X Ray Diffraction ◽  
X Ray ◽  
Mineral Phases ◽  
The World ◽  
Porosity And Permeability ◽  
First Time

This study reports for the first time the geologic occurrence of natural zeolite A and associated minerals in mudstones from the Cretaceous Paja Formation in the urban area of the municipality of Vélez (Santander), Colombia. These rocks are mainly composed of quartz, muscovite, pyrophyllite, kaolinite and chlorite group minerals, framboidal and cubic pyrite, as well as marcasite, with minor feldspar, sulphates, and phosphates. Total organic carbon (TOC), total sulfur (TS), and millimeter fragments of algae are high, whereas few centimeters and not biodiverse small ammonite fossils, and other allochemical components are subordinated. Na–A zeolite and associated mineral phases as sodalite occur just beside the interparticle micropores (honeycomb from framboidal, cube molds, and amorphous cavities). It is facilitated by petrophysical properties alterations, due to processes of high diagenesis, temperatures up to 80–100 °C, with weathering contributions, which increase the porosity and permeability, as well as the transmissivity (fluid flow), allowing the geochemistry remobilization and/or recrystallization of pre-existing silica, muscovite, kaolinite minerals group, salts, carbonates, oxides and peroxides. X-ray diffraction analyses reveal the mineral composition of the mudstones and scanning electron micrographs show the typical cubic morphology of Na–A zeolite of approximately 0.45 mμ in particle size. Our data show that the sequence of the transformation of phases is: Poorly crystalline aluminosilicate → sodalite → Na–A zeolite. A literature review shows that this is an unusual example of the occurrence of natural zeolites in sedimentary marine rocks recognized around the world.

scholarly journals Combined Influence of Low-Grade Metakaolins and Natural Zeolite on Compressive Strength and Heavy Metal Adsorption of Geopolymers

Minerals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 486
Author(s):  
Alcina Johnson Sudagar ◽  
Slávka Andrejkovičová ◽  
Fernando Rocha ◽  
Carla Patinha ◽  
Maria R. Soares ◽  
...  
Keyword(s):  
Heavy Metals ◽  
Heavy Metal ◽  
Compressive Strength ◽  
Natural Zeolite ◽  
Metal Adsorption ◽  
Low Grade ◽  
Heavy Metal Adsorption ◽  
Adsorption Model ◽  
X Ray ◽  
Adsorption Capacities

Metakaolins (MKs) prepared from low-grade kaolins located in the Alvarães (A) and Barqueiros (B) regions of Portugal were used as the aluminosilicate source to compare their effect on the compressive strength and heavy metal adsorption of geopolymers. Natural zeolite, an inexpensive, efficient adsorbent, was used as an additive in formulations to enhance geopolymers’ adsorption capacities and reduce MK utilization’s environmental footprint. Geopolymers were synthesized with the replacement of MK by zeolite up to 75 wt.% (A25, B25—25% MK 75% zeolite; A50, B50—50% MK 50% zeolite; A75, B75—75% MK 25% zeolite; A100, B100—100% MK). The molar ratios of SiO2/Al2O3 and Na2O/Al2O3 were kept at 1 to reduce the sodium silicate and sodium hydroxide environmental impact. Geopolymers’ crystallography was identified using X-ray diffraction analysis. The surface morphology was observed by scanning electron microscopy to understand the effect of zeolite incorporation. Chemical analysis using X-ray fluorescence spectroscopy and energy dispersive X-ray spectroscopy yielded information about the geopolymers’ Si/Al ratio. Compressive strength values of geopolymers obtained after 1, 14, and 28 days of curing indicate high strengths of geopolymers with 100% MK (A100—15.4 MPa; B100—32.46 MPa). Therefore, zeolite did not aid in the improvement of the compressive strength of both MK-based geopolymers. The heavy metal (Cd2+, Cr3+, Cu2+, Pb2+, and Zn2+) adsorption tests exhibit relatively higher adsorption capacities of Barqueiros MK-based geopolymers for all the heavy metals except Cd2+. Moreover, zeolite positively influenced divalent cations’ adsorption on the geopolymers produced from Barqueiros MK as B75 exhibits the highest adsorption capacities, but such an influence is not observed for Alvarães MK-based geopolymers. The general trend of adsorption of the heavy metals of both MK-based geopolymers is Pb2+ > Cd2+ > Cu2+ > Zn2+ > Cr3+ when fitted by the Langmuir isotherm adsorption model. The MK and zeolite characteristics influence geopolymers’ structure, strength, and adsorption capacities.

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