Fatty acid methyl esters (FAME) were produced from palm oil using eggshell modified with magnesium and potassium nitrates to form a composite, low-cost heterogeneous catalyst for transesterification. The catalyst, prepared by the combination of impregnation/co-precipitation was calcined at 830 °C for 4 h. Transesterification was conducted at a constant temperature of 65 °C in a batch reactor. Design of experiment (DOE) was used to optimize the reaction parameters, and the conditions that gave highest yield of FAME (85.8%) was 5.35 wt.% catalyst loading at 4.5 h with 16:1 methanol/oil molar ratio. The results revealed that eggshell, a solid waste, can be utilized as low-cost catalyst after modification with magnesium and potassium nitrates for biodiesel production.
The potential of Mg(x)Co(2-)(x)O(2) as heterogeneous reusable catalyst in transesterification of palm oil to methyl ester was investigated. The catalyst was prepared via co-precipitation of the metal hydroxides at different Mg-Co ratios. Mg(1.7)Co(0.3)O(2) catalyst was more active than Mg(0.3)Co(1.7)O(2) in the transesterification of palm oil with methanol. The catalysts calcined at temperature 300 °C for 4 h resulted in highly active oxides and the highest transesterification of 90% was achieved at methanol/oil molar ratio of 9:1, catalyst loading of 5.00 wt.%, reaction temperature of 150 °C and reaction time of 2 h. The catalyst could easily be removed from reaction mixture, but showed 50% decrease in activity when reused due to leaching of active sites.
Preparation of activated carbon has been attempted using KOH as activating agent by microwave heating from biodiesel industry solid residue, oil palm empty fruit bunch (EFBAC). The significance of chemical impregnation ratio (IR), microwave power and activation time on the properties of activated carbon were investigated. The optimum condition has been identified at the IR of 1.0, microwave power of 600 W and activation time of 7 min. EFBAC was characterized by scanning electron microscopy, Fourier transform infrared spectroscopy and nitrogen adsorption isotherm. The surface chemistry was examined by zeta potential measurement, determination of surface acidity/basicity, while the adsorptive property was quantified using methylene blue as dye model compound. The optimum conditions resulted in activated carbon with a monolayer adsorption capacity of 395.30 mg/g and carbon yield of 73.78%, while the BET surface area and total pore volume were corresponding to 1372 m2/g and 0.76 cm3/g, respectively.
Rice husk (RH), an abundant by-product of rice milling, was used for the preparation of activated carbon (RHAC) via KOH and K(2)CO(3) chemical activation. The activation process was performed at the microwave input power of 600 W for 7 min. RHACs were characterized by low temperature nitrogen adsorption/desorption, scanning electron microscopy and Fourier transform infrared spectroscopy. The adsorption behavior was examined using methylene blue as adsorbate. The K(2)CO(3)-activated sample showed higher yield and better pore structures and adsorption capacity development than the KOH-activated sample, with a BET surface area, total pore volume and monolayer adsorption capacity of 1165 m(2)/g, 0.78 cm(3)/g and 441.52 mg/g, respectively. The results revealed the feasibility of microwave heating for preparation of high surface area activated carbons from rice husks via K(2)CO(3) activation.
Oxygenated fuel additives can be produced by acetylation of glycerol. A 91% glycerol conversion with a selectivity of 38%, 28% and 34% for mono-, di- and triacetyl glyceride, respectively, was achieved at 120 °C and 3 h of reaction time in the presence of a catalyst derived from activated carbon (AC) treated with sulfuric acid at 85 °C for 4h to introduce acidic functionalities to its surface. The unique catalytic activity of the catalyst, AC-SA5, was attributed to the presence of sulfur containing functional groups on the AC surface, which enhanced the surface interaction between the glycerol molecule and acyl group of the acetic acid. The catalyst was reused in up to four consecutive batch runs and no significant decline of its initial activity was observed. The conversion and selectivity variation during the acetylation is attributed to the reaction time, reaction temperature, catalyst loading and glycerol to acetic acid molar ratio.
Fatty acid methyl ester was produced from used vegetable cooking oil using Mg(1-)(x) Zn(1+)(x)O(2) solid catalyst and the performance monitored in terms of ester content obtained. Used vegetable cooking oil was employed to reduce operation cost of biodiesel. The significant operating parameters which affect the overall yield of the process were studied. The highest ester content, 80%, was achieved with the catalyst during 4h 15 min reaction at 188°C with methanol to oil ratio of 9:1 and catalyst loading of 2.55 wt% oil. Also, transesterification of virgin oil gave higher yield with the heterogeneous catalyst and showed high selectivity towards ester production. The used vegetable cooking oil did not require any rigorous pretreatment. Catalyst stability was examined and there was no leaching of the active components, and its performance was as good at the fourth as at the first cycle.
Water scarcity and pollution rank equal to climate change as the most urgent environmental turmoil for the 21st century. To date, the percolation of textile effluents into the waterways and aquifer systems, remain an intricate conundrum abroad the nations. With the renaissance of activated carbon, there has been a steadily growing interest in the research field. Recently, the adoption of titanium dioxide, a prestigious advanced photo-catalyst which formulates the new growing branch of activated carbon composites for enhancement of adsorption rate and discoloration capacity, has attracted stern consideration and supports worldwide. Confirming the assertion, this paper presents a state of art review of titanium dioxide/activated carbon composites technology, its fundamental background studies, and environmental implications. Moreover, its major challenges together with the future expectation are summarized and discussed. Conclusively, the expanding of activated carbons composites material represents a potentially viable and powerful tool, leading to the plausible improvement of environmental conservation.
In this study, methyl ester (ME) was produced by transesterification of palm oil (CPO) (cooking grade) using activated carbon supported calcium oxide as a solid base catalyst (CaO/AC). Response surface methodology (RSM) based on central composite design (CCD) was used to optimize the effect of reaction time, molar ratio of methanol to oil, reaction temperature and catalyst amount on the transesterification process. The optimum condition for CPO transesterification to methyl ester was obtained at 5.5 wt.% catalyst amount, 190°C temperature, 15:1 methanol to oil molar ratio and 1 h 21 min reaction time. At the optimum condition, the ME content was 80.98%, which is well within the predicted value of the model. Catalyst regeneration studies indicate that the catalyst performance is sustained after two cycles.
Titanium dioxide (TiO(2)) with an enhanced photocatalytic activity was developed by doping it with calcium ions through a sol-gel method. The developed photocatalysts were characterized by Fourier transform infrared (FTIR) spectroscopy, N(2) physisorption, X-ray photoelectron spectroscopy (XPS), and X-ray diffraction. Their surface morphologies were studied using surface scanning electron microscopy (SEM). The XPS analyses confirmed the presence of Ti, O, Ca, and C in the Ca-doped TiO(2) sample. The activities of the catalysts were evaluated by photocatalytic degradation of an azo dye, acid red 1 (AR1), using UV light irradiation. The results of the investigations revealed that the samples calcined at 300 °C for 3.6h in a cyclic (2 cycles) mode had the best performance. Lower percentage dopant, 0.3-1.0 wt.%, enhanced the photocatalytic activity of TiO(2), with the best at 0.5 wt.% Ca-TiO(2). The performance of 0.5 wt.% Ca-TiO(2) in the degradation of AR1 was far superior to that of a commercial anatase TiO(2) Sigma product CAS No. 1317-70-0. The effect of pH on the degradation of AR1 was studied, and the pH of the dye solution exerted a great influence on the degradation of the dye.
Over the past couple of years, the resurgence of placing an effective and sustainable amendment to combat against the auxiliary industrial entities, remains a highly contested agenda from a global point. With the renaissance of activated carbon, there has been a steadily growing interest in the research field. Recently, the adoption of zeolite composite, a prestigious advanced catalyst which formulates the enhancement of adsorption rate and hydrogen storage capability, has fore fronted to be a new growing branch in the scientific community. Confirming the assertion, this paper presents a state of art review of activated carbon/zeolite composite technology, its fundamental background studies, and environmental implications. Moreover, its major challenges together with the future expectation are summarized and discussed. Conclusively, the expanding of activated carbon/zeolite composite represents a potentially viable and powerful tool, leading to the plausible improvement of environmental preservation.
Concern about environmental protection has increased over the years from a global viewpoint. To date, the infiltration of oil palm ash into the groundwater tables and aquifer systems which poses a potential risk and significant hazards towards the public health and ecosystems, remain an intricate challenge for the 21st century. With the revolution of biomass reutilization strategy, there has been a steadily growing interest in this research field. Confirming the assertion, this paper presents a state of art review of oil palm ash industry, its fundamental characteristics and environmental implications. Moreover, the key advance of its implementations, major challenges together with the future expectation are summarized and discussed. Conclusively, the expanding of oil palm ash in numerous field of application represents a plausible and powerful circumstance, for accruing the worldwide environmental benefit and shaping the national economy.
Stepping into the new globalizes and paradigm shifted era, a huge revolution has been undergone by the electrochemical industry. From a humble candidate of the superconductor resources, today electrosorption has demonstrated its wide variety of usefulness, almost in every part of the environmental conservation. With the renaissance of activated carbon (AC), there has been a steadily growing interest in this research field. The paper presents a state of art review of electrosorption technology, its background studies, fundamental chemistry and working principles. Moreover, recent development of the activated carbon assisted electrosorption process, its major challenges together with the future expectation are summarized and discussed. Conclusively, the expanding of electrosorption in the field of adsorption science represents a potentially viable and powerful tool, leading to the superior improvement of pollution control and environmental preservation.
Water scarcity and pollution rank equal to climate change as the most urgent environmental issue for the 21st century. To date, the percolation landfill leachate into the groundwater tables and aquifer systems which poses a potential risk and potential hazards towards the public health and ecosystems, remains an aesthetic concern and consideration abroad the nations. Arising from the steep enrichment of globalization and metropolitan growth, numerous mitigating approaches and imperative technologies have currently drastically been addressed and confronted. Confirming the assertion, this paper presents a state of art review of leachate treatment technologies, its fundamental background studies, and environmental implications. Moreover, the key advance of activated carbons adsorption, its major challenges together with the future expectation are summarized and discussed. Conclusively, the expanding of activated carbons adsorption represents a potentially viable and powerful tool, leading to the superior improvement of environmental conservation.
In this work, activated carbon was prepared from banana stalks (BSAC) waste to remove the insecticide carbofuran from aqueous solutions. The effects of contact time, initial carbofuran concentration, solution pH and temperature (30, 40 and 50 degrees C) were investigated. Adsorption isotherm, kinetics and thermodynamics of carbofuran on BSAC were studied. Equilibrium data were fitted to the Langmuir, Freundlich and Temkin isotherm models and the data best represented by the Langmuir isotherm. Thermodynamic parameters such as standard enthalpy (DeltaH(o)), standard entropy (DeltaS(o)) and standard free energy (DeltaG(o)) were evaluated. Regeneration efficiency of spent BSAC was studied using ethanol as a solvent. The efficiency was found to be in the range of 96.97-97.35%. The results indicated that the BSAC has good regeneration and reusability characteristics and can be used as alternative to present commercial activated carbon.
In this work, the adsorption potential of bamboo waste based granular activated carbon (BGAC) to remove C.I. Reactive Black (RB5) from aqueous solution was investigated using fixed-bed adsorption column. The effects of inlet RB5 concentration (50-200mg/L), feed flow rate (10-30 mL/min) and activated carbon bed height (40-80 mm) on the breakthrough characteristics of the adsorption system were determined. The highest bed capacity of 39.02 mg/g was obtained using 100mg/L inlet dye concentration, 80 mm bed height and 10 mL/min flow rate. The adsorption data were fitted to three well-established fixed-bed adsorption models namely, Adam's-Bohart, Thomas and Yoon-Nelson models. The results fitted well to the Thomas and Yoon-Nelson models with coefficients of correlation R(2)>or=0.93 at different conditions. The BGAC was shown to be suitable adsorbent for adsorption of RB5 using fixed-bed adsorption column.
Concern about environmental protection has increased over the years from a global viewpoint. To date, the percolation of pesticide waste into the groundwater tables and aquifer systems remains an aesthetic issue towards the public health and food chain interference. With the renaissance of activated carbon, there has been a consistent growing interest in this research field. Confirming the assertion, this paper presents a state of art review of pesticide agrochemical practice, its fundamental characteristics, background studies and environmental implications. Moreover, the key advance of activated carbon adsorption, its major challenges together with the future expectation are summarized and discussed. Conclusively, the expanding of activated carbon adsorption represents a plausible and powerful circumstance, leading to the superior improvement of environmental preservation.
Oil palm fronds (OPF) were used to prepare activated carbon (PFAC) using physiochemical activation method, which consisted of potassium hydroxide (KOH) treatment and carbon dioxide gasification. The effects of the preparation variables, which were activation temperature, activation time and chemical impregnation ratios (KOH: char by weight), on the carbon yield and bentazon removal were investigated. Based on the central composite design (CCD), two factor interaction (2FI) and quadratic models were, respectively, employed to correlate the PFAC preparation variables to the bentazon removal and carbon yield. From the analysis of variance (ANOVA), the most influential factor on each experimental design response was identified. The optimum conditions for preparing activated carbon from OPF were found as follows: activation temperature of 850 degrees C, activation time of 1h and KOH:char ratio of 3.75:1. The predicted and experimental results for removal of bentazon and yield of PFAC were 99.85%, 20.5 and 98.1%, 21.6%, respectively.
This study deals with the use of activated carbon prepared from bamboo waste (BMAC), as an adsorbent for the removal of chemical oxygen demand (COD) and color of cotton textile mill wastewater. Bamboo waste was used to prepare activated carbon by chemical activation using phosphoric acid (H(3)PO(4)) as chemical agent. The effects of three preparation variables activation temperature, activation time and H(3)PO(4):precursor (wt%) impregnation ratio on the color and COD removal were investigated. Based on the central composite design (CCD) and quadratic models were developed to correlate the preparation variables to the color and COD. From the analysis of variance (ANOVA), the most influential factor on each experimental design response was identified. The optimum condition was obtained by using temperature of 556 degrees C, activation time of 2.33 h and chemical impregnation ratio of 5.24, which resulted in 93.08% of color and 73.98% of COD.
In this work, activated carbon was prepared from bamboo waste by chemical activation method using phosphoric acid as activating agent. The activated carbon was evaluated for chemical oxygen demand (COD) and color reduction of a real textile mill effluent. A maximum reduction in color and COD of 91.84% and 75.21%, respectively was achieved. As a result, the standard B discharge limit of color and COD under the Malaysian Environmental Quality act 1974 was met. The Freundlich isotherm model was found best to describe the obtained equilibrium adsorption data at 30 degrees C. The Brunauer-Emmett-Teller (BET) surface area, total pore volume and the average pore diameter were 988.23 m(2)/g, 0.69 cm(3)/g and 2.82 nm, respectively. Various functional groups on the prepared bamboo activated carbon (BAC) were determined from the FTIR results.
Concern about environmental protection has aroused over the years from a global viewpoint. To date, the ever-increasing importance of biomass as the energy and material resources has lately been accounted by the rising prices for the crude petroleum oil. Rice husk ash, the most appropriate representative of the high ash biomass waste, is currently obtaining sufficient attraction, owning to its wide usefulness and potentiality in environmental conservation. Confirming the assertion, this paper presents a state of the art review of the rice milling industry, its background studies, fundamental properties and industrial applications. Moreover, the key advance on the preparation of novel adsorbents, its major challenges together with the future expectation has been highlighted and discussed. Conclusively, the expanding of rice husk ash in the field of adsorption science represents a viable and powerful tool, leading to the superior improvement of pollution control and environmental preservation.