scholarly journals Conversion of Carbohydrates (Glucose and Fructose) into 5-HMF over Solid Acid Loaded Natural Zeolite (PMA/NZ) Catalyst

2022 ◽  
pp. 100119
Author(s):  
Sonal Gupta ◽  
A.B. Gambhire ◽  
Renuka Jain
Keyword(s):  
2012 ◽  
Vol 27 (2) ◽  
pp. 129-133
Author(s):  
Yi-Fan ZHENG ◽  
Na ZHAO ◽  
Jie ZHANG ◽  
Xiao-Ye YU ◽  
Wei-Min MO
Keyword(s):  

1992 ◽  
Vol 26 (9-11) ◽  
pp. 2269-2272 ◽  
Author(s):  
Š Cerjan-Stefanovic ◽  
M. Kaštelan-Macan ◽  
T. Filipan

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.


Author(s):  
Reza Yazdanpanah ◽  
Eshagh Moradiyan ◽  
Rouein Halladj ◽  
Sima Askari

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.


Author(s):  
Charishma Venkata Sai Anne ◽  
Karthikeyan S. ◽  
Arun C.

Background: Waste biomass derived reusable heterogeneous acid based catalysts are more suitable to overcome the problems associated with homogeneous catalysts. The use of agricultural biomass as catalyst for transesterification process is more economical and it reduces the overall production cost of biodiesel. The identification of an appropriate suitable catalyst for effective transesterification will be a landmark in biofuel sector Objective: In the present investigation, waste wood biomass was used to prepare a low cost sulfonated solid acid catalyst for the production of biodiesel using waste cooking oil. Methods: The pretreated wood biomass was first calcined then sulfonated with H2SO4. The catalyst was characterized by various analyses such as, Fourier-transform infrared spectroscopy (FTIR), Scanning Electron Microscopy (SEM), Energy Dispersive X-Ray Spectroscopy (EDS) and X-ray diffraction (XRD). The central composite design (CCD) based response surface methodology (RSM) was applied to study the influence of individual process variables such as temperature, catalyst load, methanol to oil molar ration and reaction time on biodiesel yield. Results: The obtained optimized conditions are as follows: temperature (165 ˚C), catalyst loading (1.625 wt%), methanol to oil molar ratio (15:1) and reaction time (143 min) with a maximum biodiesel yield of 95 %. The Gas chromatographymass spectrometry (GC-MS) analysis of biodiesel produced from waste cooking oil was showed that it has a mixture of both monounsaturated and saturated methyl esters. Conclusion: Thus the waste wood biomass derived heterogeneous catalyst for the transesterification process of waste cooking oil can be applied for sustainable biodiesel production by adding an additional value for the waste materials and also eliminating the disposable problem of waste oils.


2015 ◽  
Vol 2 (2) ◽  
Author(s):  
Wahyu Wilopo ◽  
Septiawan Nur Haryono ◽  
Doni Prakasa Eka Putra ◽  
I Wayan Warmada ◽  
Tsuyoshi Hirajima

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


1992 ◽  
Vol 57 (11) ◽  
pp. 2241-2247 ◽  
Author(s):  
Tomáš Hochmann ◽  
Karel Setínek

Solid acid catalysts with acid strength of -14.52 < H0 < -8.2 were prepared by sulfate treatment of the samples of boehmite calcined at 105-800 °C. Two preparation methods were used: impregnation of the calcined boehmite with 3.5 M H2SO4 or mixing of the boehmite samples with anhydrous aluminum sulfate, in both cases followed by calcination in nitrogen at 650 °C. The catalysts were characterized by measurements of surface area, adsorption of pyridine and benzene, acid strength measurements by the indicator method and by catalytic activity tests in the isomerization of cyclohexene, p-xylene and n-hexane. Properties of the catalysts prepared by both methods were comparable.


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