Carboxylate-Alumoxanes: Precursors for Heterogeneous Catalysts

1999 ◽  
Vol 581 ◽  
Author(s):  
Christopher D. Jones ◽  
David S. Brown ◽  
Larry L Marshall ◽  
Andrew R. Barrona

ABSTRACTCarboxylate-alumoxanes are organic substituted alumina nano-particles synthesized from boehmite in aqueous solution which are an inexpensive and environmentally benign precursor for the fabrication of nano-, meso-, and macro-scale aluminum based ceramics. The use of carboxylate-alumoxanes as a novel high surface area alumina support for heterogeneous catalysis will be discussed. The ability to perform further chemistry on the organic ligands of the carboxylate-alumoxanes allows for attachment of catalysts. During calcination, the organic ligands are burned out, leaving behind the catalyst in a well-dispersed manner. To demonstrate this concept, the metathesis of C16 olefins using a molybdenum oxide catalyst supported on alumina will be discussed using the carboxylate-alumoxane method.

Author(s):  
A. K. Datye ◽  
D. S. Kalakkad ◽  
L. F. Allard ◽  
E. Völkl

The active phase in heterogeneous catalysts consists of nanometer-sized metal or oxide particles dispersed within the tortuous pore structure of a high surface area matrix. Such catalysts are extensively used for controlling emissions from automobile exhausts or in industrial processes such as the refining of crude oil to produce gasoline. The morphology of these nano-particles is of great interest to catalytic chemists since it affects the activity and selectivity for a class of reactions known as structure-sensitive reactions. In this paper, we describe some of the challenges in the study of heterogeneous catalysts, and provide examples of how electron holography can help in extracting details of particle structure and morphology on an atomic scale.Conventional high-resolution TEM imaging methods permit the image intensity to be recorded, but the phase information in the complex image wave is lost. However, it is the phase information which is sensitive at the atomic scale to changes in specimen thickness and composition, and thus analysis of the phase image can yield important information on morphological details at the nanometer level.


Toxics ◽  
2021 ◽  
Vol 9 (8) ◽  
pp. 175
Author(s):  
Sang-Eun Jo ◽  
Jung-Weon Choi ◽  
Sang-June Choi

Mag@silica-Ag composite has a high sorption ability for I− in aqueous solution due to its high surface area and strong affinity for the studied anion. The material adsorbed I− rapidly during the initial contact time (in 45 min, η = 80%) and reached adsorption equilibrium after 2 h. Moreover, mag@silica-Ag proved to selectively remove I− from a mixture of Cl−, NO3− and I−. The adsorption behavior fitted the Langmuir isotherm perfectly and the pseudo-second-order kinetic model. Based on the Langmuir isotherm, the maximum adsorption capacity of mag@silica-Ag was 0.82 mmol/g, which is significantly higher than previously developed adsorbents. This study introduces a practical application of a high-capacity adsorbent in removing radioactive I− from wastewaters.


2013 ◽  
Vol 798-799 ◽  
pp. 1123-1127
Author(s):  
Hua Lei Zhou ◽  
Qiong Qiong Zhu ◽  
Dong Hua Huang

The activated carbon with high surface area was prepared by KOH activation from anthracite and used as adsorbent for removal of Cr (VI) from aqueous solution. The pore structure and surface properties were characterized by N2 adsorption at 77K, transmission electron microscope (TEM) and Fourier transform infrared spectroscopy ( FTIR). Effect of pH and isotherms at different temperature were investigated. Results show that the prepared carbon is a microporous-and mesoporous-adsorbent with developed pore structure and abundant surface oxygen-containing groups. PH value of the solution plays key function on the adsorption. The chemical adsorption dominates the adsorption process. The activated carbon exhibits much higher Cr adsorption capacity than the commercial activated carbon at initial pH of ~3. The equilibrium adsorption data are fitted by both Freundlich model and Langmuir model well.


2021 ◽  
Vol 2021 ◽  
pp. 1-10
Author(s):  
Dhiraj Dutta ◽  
Jyoti Prasad Borah ◽  
Amrit Puzari

Results of investigation on adsorption of Mn2+ from aqueous solution by manganese oxide-coated hollow polymethylmethacrylate microspheres (MHPM) are reported here. This is the first report on Mn-coated hollow polymer as a substitute for widely used materials like green sand or MN-coated sand. Hollow polymethylmethacrylate (HPM) was prepared by using a literature procedure. Manganese oxide (MnO) was coated on the surface of HPM (MHPM) by using the electroless plating technique. The HPM and MHPM were characterized by using optical microscopy (OM), scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and thermogravimetric analysis (TGA). Optical and scanning micrographs were used to monitor the surface properties of the coated layer which revealed the presence of MnO on the surface of HPM. TGA showed the presence of 4-5% of MnO in MHPM. Adsorption isotherm studies were carried out as a function of pH, initial ion concentration, and contact time, to determine the adsorption efficiency for removal of Mn2+ from contaminated water by the synthesized MHPM. The isotherm results showed that the maximum adsorption capacity of MnO-coated HPM to remove manganese contaminants from water is 8.373 mg/g. The obtained R 2 values of Langmuir isotherm and Freundlich isotherm models were 1 and 0.87, respectively. Therefore, R 2 magnitude confirmed that the Langmuir model is best suited for Mn2+ adsorption by a monolayer of MHPM adsorbent. The material developed shows higher adsorption capacity even at a higher concentration of solute ions, which is not usually observed with similar materials of this kind. Overall findings indicate that MHPM is a very potential lightweight adsorbent for removal of Mn2+ from the aqueous solution because of its low density and high surface area.


2018 ◽  
Vol 22 (2) ◽  
pp. 109-116
Author(s):  
Bhishma Karki ◽  
Jeevan Jyoti Nakarmi ◽  
Rhiddi Bir Singh ◽  
Manish Banerjee

The synthesis of functional nano-particles via spray pyrolysis technique (SPT), especially those of catalytic nature, has attracted the interests of scientists and engineers, as well as industries. The rapid and high temperature continuous synthesis yields nano-particles with intrinsic features of active catalysts, that is, high surface area and surface energetic. For these reasons, SPT finds applications in various thermally inducible catalytic reactions. However, the design and synthesis of photocatalysts by SPT requires a knowledge set which is different from that established for thermal catalysts. Unknown to many, this has resulted in frustrations to those entering the field unprepared, especially since SPT appears to be an elegant tool in synthesizing oxide nano-particles of any elemental construct. From simple oxide to doped-oxide, and mixed metal oxide to the in situ deposition of noble metals, this Perspective gives an overview on the development of photocatalysts made by SPT in the last decade that led to a better understanding of the design criteria. Various challenges and opportunities are also highlighted; especially those beyond simple metal oxides, which perhaps contain the greatest potential for the exploitation of photocatalysts design by SPT. Journal of Institute of Science and TechnologyVolume 22, Issue 2, January 2018, Page: 109-116


2021 ◽  
Vol 01 ◽  
Author(s):  
Sharwari K. Mengane ◽  
Ronghui Wu ◽  
Liyun Ma ◽  
Chhaya S. Panse ◽  
Shailesh N. Vajekar ◽  
...  

: Catalysis is the multidisciplinary field involving many areas of chemistry, notably in organometallic chemistry and materials science. It has great applications in synthesis of many industrially applicable compounds such as fuels and fine chemicals. The activity and selectivity are a key issue in catalysis that generally allied to high surface area. The current research activities mainly deal with the homogeneous and heterogeneous catalysis. Homogeneous and heterogeneous catalysis have certain drawbacks which restricts their application to great extent but have their own advantages. Hence, it has a predominant concern of current research to find out an alternate to overcome their drawbacks. Therefore, it is highly desirable to find a catalytic protocol that offers high selectivity and excellent product yield with quick and easy recovery. Along with their various applications as alternatives to conventional bulk materials nanomaterial have established its great role in different industrial and scientific applications. Nanocatalysis has emerged as new alternative to the conventional homogeneous and heterogeneous catalysis. The nanomaterials are responsible to enhance surface area of the catalyst, which ultimately increases the catalyst reactants contacts. In addition, it acts as robust material and has high surface area like heterogeneous catalysts. Insolubility of such nanomaterial in reaction medium makes them easily separable, hence, catalyst can be easily separate from the product. Hence, it has been proven that nanocatalysts behave like homogeneous as well as heterogeneous catalysts which work as a bridge between the conventional catalytic systems. Considering these merits; researchers has paid their attention towards applications of nanocatalyst in several organic reactions. This review article focused on the catalytic applications of metal nanoparticles (MNPs) such as Pd, Ag, Au, Cu, Pt in ligand free coupling reactions. In addition, it covers applications of bimetallic and multimetallic nanoparticles in ligand free coupling reactions.


2020 ◽  
Vol 10 (3) ◽  
pp. 918 ◽  
Author(s):  
Jack Clohessy ◽  
Witold Kwapinski

In recent years, a new class of superior heterogeneous acid catalyst for biodiesel production has emerged. These catalysts offer advantages over their predecessors such as high surface area, elevated acid site density, enhanced catalyst activity, good operation stability and relevant economic affordability in an environmentally friendly frame. This review was concerned with carbon-based solid acid (CBAS) catalysts derived from both carbohydrate and pyrolysis products. A series of CBASs with various origins such as D-glucose, sucrose, starch, cellulose and vegetable oil asphalt, converted to char and sulphonated, have been explored as potential heterogeneous catalysts. Catalyst preparation and synthesis methods were briefly summarized. Catalyst characterization and performance for biofuels related reactions were elucidated, identifying potential research applications. Three catalysts in particular were identified as having potential for industrial application and requiring further research.


2014 ◽  
Vol 20 (1) ◽  
pp. 97-107 ◽  
Author(s):  
Mohammad Behnajady ◽  
Shahrzad Yavari ◽  
Nasser Modirshahla

In this work TiO2-P25 nanoparticles with high surface area have been used as adsorbent for the removal of C.I Acid Red 27 (AR27), as an organic contaminant from aqueous solution. Characteristics of phases and crystallite size of TiO2-P25 nanoparticles were achieved from XRD and the surface area and pore size distribution were obtained from BET and BJH techniques. TiO2-P25 nanoparticles with almost 80% anatase and 20% rutile phases, the average crystallite size of 18 nm, have specific surface area of 56.82 m2 g-1. The effect of various parameters like initial AR27 concentration, pH, contact time and adsorbent dosage has been carried out in order to find desired adsorption conditions. The desired pH for adsorption of AR27 onto TiO2-P25 nanoparticles was 3. The equilibrium data were analyzed with various 2-, 3- and 4-parameter isotherm models. Equilibrium data fitted very well by the 4-parameter Fritz-Schluender model. Results of adsorption kinetics study indicated that the pseudo-second order kinetics provided the best fit with correlation coefficients close to unity.


2020 ◽  
Vol 19 ◽  
pp. 100570
Author(s):  
Wimalika R.K. Thalgaspitiya ◽  
Tharindu Kankanam Kapuge ◽  
Dinithi Rathnayake ◽  
Junkai He ◽  
William S. Willis ◽  
...  

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