A New Low Cost Synthesis Method for LiFePO4

Keyword(s):  
Low Cost ◽  
2020 ◽  
Vol 18 (1) ◽  
pp. 1148-1166
Author(s):  
Ganjar Fadillah ◽  
Septian Perwira Yudha ◽  
Suresh Sagadevan ◽  
Is Fatimah ◽  
Oki Muraza

AbstractPhysical and chemical methods have been developed for water and wastewater treatments. Adsorption is an attractive method due to its simplicity and low cost, and it has been widely employed in industrial treatment. In advanced schemes, chemical oxidation and photocatalytic oxidation have been recognized as effective methods for wastewater-containing organic compounds. The use of magnetic iron oxide in these methods has received much attention. Magnetic iron oxide nanocomposite adsorbents have been recognized as favorable materials due to their stability, high adsorption capacities, and recoverability, compared to conventional sorbents. Magnetic iron oxide nanocomposites have also been reported to be effective in photocatalytic and chemical oxidation processes. The current review has presented recent developments in techniques using magnetic iron oxide nanocomposites for water treatment applications. The review highlights the synthesis method and compares modifications for adsorbent, photocatalytic oxidation, and chemical oxidation processes. Future prospects for the use of nanocomposites have been presented.


2021 ◽  
Vol 15 (2) ◽  
pp. 128-135
Author(s):  
Thaís Luiz ◽  
Fabio Nakagomi ◽  
Reny Renzetti ◽  
Guilherme Siqueira

The microwave assisted combustion synthesis (MACS) as a new, quick and low cost synthesis method was used for preparation of niobium pentoxide (Nb2O5) powders. The present paper investigated the effect of reactant concentrations (ammonium niobium oxalate, urea and ammonium nitrate) on the characteristics of Nb2O5 nanoparticles. Three samples were synthesized with stoichiometric ratio between the fuel and oxidant (C1), excess of oxidant (C2) and excess of fuel (C3). In all samples, Nb2O5 crystalline nanoparticles with irregular morphology were detected. The synthesis of nanoparticles with smaller diameter in the C2 and C3 samples was confirmed by greater values of band gap energy measured through UV-Visible diffuse reflectance spectroscopy (indicating quantum confinement) and by the Rietveld refinement of X-ray diffraction patterns. The results showed that the amounts of oxidant and fuel can change synthesis temperature, influencing the final characteristics of the particles, such as size and existent phases. In these cases the excess of oxidant and fuel in the C2 and C3 samples, respectively, decreases the average synthesis temperature and decelerates the particle growth and the formation of the monoclinic phase.


2020 ◽  
Author(s):  
Luqman Hakim Mohd Azmi ◽  
Daryl R. Williams ◽  
Bradley P. Ladewig

<div><b>Abstract</b></div><div>A new synthesis method was developed to prepare an aluminum-based metal organic framework (MIL-96) with a larger particle size and different crystal habits. A low cost and water-soluble polymer, hydrolyzed polyacrylamide (HPAM), was added in varying quantities into the synthesis reaction to achieve >200% particle size enlargement with controlled crystal morphology. The modified adsorbent, MIL-96-RHPAM2, was systematically characterized by SEM, XRD, FTIR, BET and TGA-MS. Using activated carbon (AC) as a reference adsorbent, the effectiveness of MIL-96-RHPAM2 for perfluorooctanoic acid (PFOA) removal from water was examined. The study confirms stable morphology of hydrated MIL-96-RHPAM2 particles as well as a superior PFOA adsorption capacity (340 mg/g) despite its lower surface area, relative to standard MIL-96. MIL-96-RHPAM2 suffers from slow adsorption kinetics as the modification significantly blocks pore access. The strong adsorption of PFOA by MIL-96-RHPAM2 was associated with the formation of electrostatic bonds between the anionic carboxylate of PFOA and the amine functionality present in the HPAM backbone. Thus, the strongly held PFOA molecules in the pores of MIL-96-RHPAM2 were not easily desorbed even after eluted with a high ionic strength solvent (500 mM NaCl). Nevertheless, this simple HPAM addition strategy can still chart promising pathways to impart judicious control over adsorbent particle size and crystal shapes while the introduction of amine functionality onto the surface chemistry is simultaneously useful for enhanced PFOA removal from contaminated aqueous systems.<br></div>


2020 ◽  
Author(s):  
Luqman Hakim Mohd Azmi ◽  
Daryl R. Williams ◽  
Bradley P. Ladewig

<div><b>Abstract</b></div><div>A new synthesis method was developed to prepare an aluminum-based metal organic framework (MIL-96) with a larger particle size and different crystal habits. A low cost and water-soluble polymer, hydrolyzed polyacrylamide (HPAM), was added in varying quantities into the synthesis reaction to achieve >200% particle size enlargement with controlled crystal morphology. The modified adsorbent, MIL-96-RHPAM2, was systematically characterized by SEM, XRD, FTIR, BET and TGA-MS. Using activated carbon (AC) as a reference adsorbent, the effectiveness of MIL-96-RHPAM2 for perfluorooctanoic acid (PFOA) removal from water was examined. The study confirms stable morphology of hydrated MIL-96-RHPAM2 particles as well as a superior PFOA adsorption capacity (340 mg/g) despite its lower surface area, relative to standard MIL-96. MIL-96-RHPAM2 suffers from slow adsorption kinetics as the modification significantly blocks pore access. The strong adsorption of PFOA by MIL-96-RHPAM2 was associated with the formation of electrostatic bonds between the anionic carboxylate of PFOA and the amine functionality present in the HPAM backbone. Thus, the strongly held PFOA molecules in the pores of MIL-96-RHPAM2 were not easily desorbed even after eluted with a high ionic strength solvent (500 mM NaCl). Nevertheless, this simple HPAM addition strategy can still chart promising pathways to impart judicious control over adsorbent particle size and crystal shapes while the introduction of amine functionality onto the surface chemistry is simultaneously useful for enhanced PFOA removal from contaminated aqueous systems.<br></div>


2020 ◽  
Vol 73 (7) ◽  
pp. 587
Author(s):  
Sitong Guo ◽  
Wen Tan ◽  
Jiyicheng Qiu ◽  
Jinlong Du ◽  
Zhanxu Yang ◽  
...  

As a popular material synthesis method, spatially confined reactions have been gradually recognised for their excellent performance in the field of current materials synthesis. In recent years, molybdenum-based catalysts have gradually gained recognition due to high natural reserves of Mo, its low cost, and many other advantages, and they have wide applications in the area of functional materials, especially in topical areas such as batteries and electrocatalysts. In this context, spatially confined reactions have become widely to obtain various types of molybdenum-based electrode materials and electrocatalysts which result in an excellent morphology, structure, and performance. In this review, the concept of a spatially confined reaction system and the electrochemical application (electrode materials and electrocatalyst) of molybdenum-based materials synthesised in this way are comprehensively discussed. The current problems and future development and application of molybdenum-based materials are also discussed in this review.


2008 ◽  
Vol 368-372 ◽  
pp. 1166-1168 ◽  
Author(s):  
Tao Yu ◽  
Jian Dong Ye

In this work, a simple, reproducible and low-cost synthesis method for the preparation of ß-tricalcium phosphate (ß-TCP) was developed. ß-TCP was prepared via wet mechanochemical treatment using calcium oxide and calcium hydrogen phosphate as raw materials. XRD and FTIR analysis indicated that the as-treated precursor was non-stoichiometric, poorly-crystallized carbonated hydroxyapatite (CHA) resulting from the mechanochemical reaction, and the crystalline ß-TCP powder was obtained by calcining the precursor at 800°C for 2 hours. SEM observation showed that the addition of surfactants could eliminate the agglomeration of the powder and well-dispersive ß-TCP powder with a particle diameter between 0.1 and 2.0 2m can be obtained.


2005 ◽  
Vol 127 (2) ◽  
pp. 232-241 ◽  
Author(s):  
Xichun Nie ◽  
Venkat Krovi

Single degree-of-freedom coupled serial chain (SDCSC) mechanisms are a class of mechanisms that can be realized by coupling successive joint rotations of a serial chain linkage, by way of gears or cable-pulley drives. Such mechanisms combine the benefits of single degree-of-freedom design and control with the anthropomorphic workspace of serial chains. Our interest is in creating articulated manipulation-assistive aids based on the SDCSC configuration to work passively in cooperation with the human operator or to serve as a low-cost automation solution. However, as single-degree-of-freedom systems, such SDCSC-configuration manipulators need to be designed specific to a given task. In this paper, we investigate the development of a synthesis scheme, leveraging tools from Fourier analysis and optimization, to permit the end-effectors of such manipulators to closely approximate desired closed planar paths. In particular, we note that the forward kinematics equations take the form of a finite trigonometric series in terms of the input crank rotations. The proposed Fourier-based synthesis method exploits this special structure to achieve the combined number and dimensional synthesis of SDCSC-configuration manipulators for closed-loop planar path-following tasks. Representative examples illustrate the application of this method for tracing candidate square and rectangular paths. Emphasis is also placed on conversion of computational results into physically realizable mechanism designs.


2012 ◽  
Vol 468-471 ◽  
pp. 857-862
Author(s):  
Zhen Xing Zheng

A new compaction powder metallurgy equipment integrated with the mould and the frame is introduced to substitute the traditional powder metallurgy equipment (P/M). During the design and manufacture, finite element method is used to analyze the motion of the equipment. The Lagrange equation and modal synthesis method for flexible body are constructed, and then the cooperative simulation method using ADAMS and MARC is present for solving flexible multibody dynamics of flexible body. Results show that the design of the structure of the powder metallurgy equipment is feasible and the low cost and the simple structure are its merits compared to the traditional equipment.


1997 ◽  
Vol 119 (2) ◽  
pp. 232-237 ◽  
Author(s):  
T. Chuenchom ◽  
S. Kota

Conventional hard automation such as linkage mechanisms and cam-driven mechanisms provide high speed capability at a low cost, but fail to provide the flexibility required in many industrial applications. On the other hand, for most manufacturing automation applications in high production industries, expensive multi-axis robots are employed for simple repetitive operations that require only limited flexibility. In order to provide a true middle ground between conventional mechanism-based hard automation and overly flexible anthropomorphic robots, we incorporate flexibility in conventional mechanisms, thereby creating “programmable mechanisms” or Adjustable Robotic Mechanisms (ARMs). This paper introduces the concept of ARMs and presents generalized analytical methods for designing adjustable mechanisms based on synthesis of adjustable dyads. The synthesis methods presented here, which are extensions of the well-known Burmester precision point theory, enable one to design multi-purpose mechanisms for multiple sets of precision points, thereby enabling conventional mechanisms to perform multiple tasks. The analytical synthesis method has been implemented in a computer program that generates all adjustable dyad solutions for given sets of precision points. Two or more adjustable dyads are assembled together to form a programmable linkage mechanism that performs multiple tasks. Synthesis formulations and a design example illustrating the analytical and computer-aided synthesis methods are presented.


Research ◽  
2019 ◽  
Vol 2019 ◽  
pp. 1-10
Author(s):  
Shikui Han ◽  
Kai Zhou ◽  
Yifu Yu ◽  
Chaoliang Tan ◽  
Junze Chen ◽  
...  

The layered transition metal dichalcogenides (TMDs) and transition metal phosphides are low-cost, earth-abundant, and robust electrocatalysts for hydrogen evolution reaction (HER). Integrating them into hybrid nanostructures is potentially promising to further boost the catalytic activity toward HER based on their synergistic effects. Herein, we report a general method for the synthesis of a series of MoSe2-based hybrid nanostructures, including MoSe2-Ni2P, MoSe2-Co2P, MoSe2-Ni, MoSe2-Co, and MoSe2-NiS, by postgrowth of Ni2P, Co2P, Ni, Co, and NiS nanostructures on the presynthesized MoSe2 nanosheet-assembled nanospheres, respectively, via a colloidal synthesis method. As a proof-of-concept application, the as-synthesized hybrid nanostructures are used as electrocatalysts for HER, exhibiting high activity and stability in acidic media. Among them, the MoSe2-Co2P composite shows the highest HER activity with an overpotential of 167 mV at 10 mA cm-2.


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