62 research outputs found

    One-step microalgal biodiesel production from Chlorella pyrenoidosa using subcritical methanol extraction (SCM) technology

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    In this work, we propose a one-step subcritical methanol extraction (SCM) process for biodiesel production from Chlorella pyrenoidosa. Therefore, the present study attempts to establish and determine the optimum operating conditions for maximum biodiesel yield from SCM of C. pyrenoidosa. A statistical approach, i.e. response surface methodology is employed in this study. The effects of three operational factors: reaction temperature (140–220 °C), reaction time (1–15 min) and methanol to algae ratio (1–9 wt.%) were investigated using a central composite design. A maximum yield of crude biodiesel of 7.1 wt.% was obtained at 160 °C, 3 min reaction time and 7 wt.% methanol to algae ratio. The analysis of variance revealed that methanol to algae ratio is the most significant factor for maximizing biodiesel yield. Regression analysis showed a good fit of the experimental data to the second-order polynomial model. With no requirement of catalyst nor any pretreatment step, SCM process is economically feasible to scale up the commercial biodiesel production from algae

    Removal of boron and arsenic from petrochemical wastewater using zeolite as adsorbent

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    Petrochemical wastewater is one of the major industrial concerns due to the toxicity of heavy metals such as boron and arsenic. These metals must be progressively treated before discharged into receiving water. In this research, adsorption of boron and arsenic was conducted using natural zeolite (clinoptilolite). The arsenic and boron removal efficiencies using natural zeolite as adsorbents are 66 and 52 %, respectively, at its optimum conditions (pH 8, contact time 240 min and adsorbent dosage 480 g/L). Compared to various adsorbents, the adsorption using natural zeolite showed excellent boron and arsenic removal, thus has a great potential to be applied in industrial wastewater treatment plant

    Sago wastes and its applications

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    The sago starch industry is one of the major revenue sources of the Malaysian state of Sarawak. This state is currently among the world’s leading producers of sago starch, exporting more than 40,000 tons every year to different Asian countries. This number is expected to rise since starch production and export value have been increasing 15.0%-20.0% each year. Sago palm is subjected to various processes to obtain starch from its trunk. During processing, a huge amount of residual solid wastes is generated, such as bark and hampas, and in general, is burned or washed off to nearby streams. Along with the rising sago starch demand, the sago starch industry is now facing waste management problems, which have resulted in environmental pollution and health hazards. These wastes comprise starch, hemicellulose, cellulose, and lignin; hence, can be valorized into feedstock as value-added products. To date, these wastes have been utilized in the production of many materials like adsorbents, sugars, biofuels, nanomaterials, composites, and ceramics. This review article aims to summarize the various methods by which these wastes can be utilized besides to enlighten the major interest on sago hampas and bark

    A Study on Zeolite Performance in Waste Treating Ponds for Treatment of Palm Oil Mill Effluent.

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    Oil palm currently occupies the largest acreage of farm land in Malaysia. In 2011, the production of palm oil in Malaysia was recorded as 19.8 million tons which has led to a huge amount of wastewater known as palm oil mill effluent (POME). This work focuses on the ponding system which acts as wastewater treatment plant in order to treat POME. The conventional ponding system applied in mills consists of a series of seven ponds. The maintenance costs of the pond are expensive thus study of alternative methods is needed. POME treatment using zeolite shows a potential to overcome the problem. Samples collected from selected ponds are tested and analyzed using water analyzer method. Result from adsorption by zeolite shows a significant reduction of COD, BOD, Fe, Zn, Mn and turbidity. This shows that zeolite is highly potential to be applied as adsorbent in the POME treatment plants. The results here may lead to lower maintenance cost, lower quantity of treatment ponds and lesser land occupied for the treatment of POME in Malaysia

    Recovery of palm oil and valuable material from oil palm empty fruit bunch by sub-critical water

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    Oil palm empty fruit bunch (EFB) is one of the solid wastes produced in huge volume by palm oil mill. Whilst it still contains valuable oil, approximately 22.6 million tons is generated annually and treated as solid waste. In this work, sub-critical water (sub-cw) was used to extract oil, sugar and tar from spikelet of EFB. The spikelet was treated with sub-cw between 180-280°C and a reaction time of 2 and 5 minutes. The highest yield of oil was 0.075 g-oil/g-dry EFB, obtained at 240°C and reaction time of 5 minutes. Astonishingly, oil that was extracted through this method was 84.5% of that obtained through Soxhlet method using hexane. Yield of oil extracted was strongly affected by the reaction temperature and time. Higher reaction temperature induces the dielectric constant of water towards the non-polar properties of solvent; thus increases the oil extraction capability. Meanwhile, the highest yield of sugar was 0.20 g-sugar/g-dry EFB obtained at 220°C. At this temperature, the ion product of water is high enough to enable maximum sub-critical water hydrolysis reaction. This study showed that oil and other valuable material can be recovered using water at sub-critical condition, and most attractive without the use of harmful organic solvent

    Adsorption process of heavy metals by low-cost adsorbent: a review

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    In this article, the potential of various low-cost adsorbents for the removal of heavy metals from contaminated water has been reviewed. Various conventional methods for heavy metal removal such as precipitation, evaporation, electroplating and also ion exchange have been applied since previous years. However, these methods have several disadvantages such as only limited to certain concentrations of metals ions, generation large amount of toxic sludge and the capital costs are much too high to be economical. Hence, adsorption using low-cost adsorbents is found to be more environmentally friendly. Adsorption is the alternative process, for heavy metal removal due to the wide number of natural materials or agricultural wastes gathering in abundance from our environment. High adsorption capacities, cost effectiveness and their abundance in nature are the important parameters which explain why the adsorbent is economical for heavy metal removal. In this review, a list of adsorbent literature has been compiled to provide a summary of available information on a wide range of low cost adsorbents for removing heavy metals from contaminated water. The application of available adsorption models such as the isotherm, kinetics and thermodynamics as well as the influence of parameters on metal adsorption by low cost adsorbent shall be reviewed to understand the adsorption mechanism of low-cost adsorbents

    Hydrolysis of blended cotton/polyester fabric from hospital waste using subcritical water

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    Currently in Malaysia, most wastes are disposed into poorly managed systems with little or no pollution protection measures. Large amounts of wastes such as textiles are generated through hospitals and health care centers. However, the improper management of these abundantly generated wastes may pose an environmental pollution problems and fire hazard. Cotton textile is a potential biomass for bioethanol production. Subcritical water (Sub-CW) hydrolysis was investigated as an alternative technology for the recycling of cotton textile waste for current health care waste management. The aim of this study was to investigate the possibility of complete conversion of cotton textile waste to ethanol via Sub-CW hydrolysis and fermentation. Sub-CW was carried out to facilitate the hydrolysis of cellulose component in cotton textile (cotton 75%+polyester 25%). The study was divided into two parts; (i) To evaluate the subcritical water parameters such as temperature and time to achieve maximum yield of sugars. (ii) Fermentation of the hydrolysate obtained from Sub-CW hydrolysis to ethanol. Under Sub-CW conditions of temperature (140 °C - 350 °C), reaction time (1-10 min) and water to cotton ratio (3:1) showed that cotton textile treated at 280 °C for 4 min, was optimal for maximizing yield of sugar, which was 0.213 g/g-dry sample. The quantitative analysis by HPLC showed that the soluble carbohydrates in the water phase were mainly composed of glucose. The obtained glucose concentration, 171 mg/L was then fermented at 36 °C for 24 hours by Saccharomyces cerevisae (yeast) to ethanol. Highest yield of ethanol was 0.415 g/g glucose, which was 81.2 % of theoretical yield. Hydrolysis with Sub-CW showed the potential to decompose the cotton textile into simple sugar while keeping sugar degradation to minimal phase and the possibility of complete conversion of cotton textile waste to ethanol via Sub-CW and fermentation

    Study the thermal stability of nitrogen doped reduced graphite oxide supported copper catalyst

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    The thermal stability of the as-synthesized Nitrogen-doped reduced graphite oxide supported copper catalyst was investigated by a thermogravimetric analyzer (TGA) at a temperature range 273–1173 K under purified N2 atmosphere using three different heating rates (15, 20 and 25 K min−1). Firstly, to obtained nitrogen-doped reduced graphite oxide (N-rGO), the functionalized graphite oxide was synthesized using Staudenmaier’s method reduced by continuously stirring in an ammonia solution subsequently. The rGO was doped with nitrogen and impregnated with Cu-precursor to obtain Cu/N-rGO. The as-synthesized GO; N-rGO and Cu/N-rGO were characterized by FESEM, EDX, TEM, XRD and XPS. All these analyses were resulted in successfully samples synthesized. The TGA kinetic data were fitted into Kissinger and Flynn–Wall–Ozawa model free expressions to obtain apparent activation energies of 83.34 and 102.59 J mol−1 and pre-exponential factors of 2.40 × 107 and 5.01 × 1011 s−1. The high R2 values of 0.9999 and 0.9666 obtained from fitting TGA kinetic data using the Kissinger and Flynn–Wall–Ozawa model free expressions show that the data were well fitted to the expressions. This implies that the thermal behavior of nitrogen doped reduced graphite oxide supported Cu catalyst can be investigated using Kissinger and Flynn–Wall–Ozawa model free expressions

    Dehydrogenation of Cyclohexanol to Cyclohexanone Over Nitrogen-doped Graphene supported Cu catalyst

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    In this study, the dehydrogenation of cyclohexanol to cyclohexanone over nitrogen-doped reduced graphene oxide (N-rGO) Cu catalyst has been reported. The N-rGO support was synthesized by chemical reduction of graphite oxide (GO). The synthesized N-rGO was used as a support to prepare the Cu/N-rGO catalyst via an incipient wet impregnation method. The as-prepared support and the Cu/N-rGO catalyst were characterized by FESEM, EDX, XRD, TEM, TGA, and Raman spectroscopy. The various characterization analysis revealed the suitability of the Cu/N-rGO as a heterogeneous catalyst that can be employed for the dehydrogenation of cyclohexanol to cyclohexanone. The catalytic activity of the Cu/N-rGO catalyst was tested in non-oxidative dehydrogenation of cyclohexanol to cyclohexanone using a stainless-steel fixed bed reactor. The effects of temperature, reactant flow rate, and time-on-stream on the activity of the Cu/N-rGO catalyst were examined. The Cu/N-rGO nanosheets show excellent catalytic activity and selectivity to cyclohexanone. The formation of stable Cu nanoparticles on N-rGO support interaction and segregation of Cu were crucial factors for the catalytic activity. The highest cyclohexanol conversion and selectivity of 93.3% and 82.7%, respectively, were obtained at a reaction temperature of 270 °C and cyclohexanol feed rate of 0.1 ml/min. Copyright © 2020 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

    Removal and recovery attempt of liquid crystal from waste LCD panels using subcritical water

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    With the advancement of the fourth industrial revolution, the demand for LCD has widely accelerated as monitoring screens for computers and cell phones. Consequently, old LCD panels are expected to end up as a tremendous amount of e-waste. Apart from transparent electrodes and transistor, waste LCD panel also contains hazardous liquid crystal compound that can contaminate the landfill site. Thus, removing the material from waste LCD was investigated. In this study, water at subcritical state was applied at temperatures between 100 and 360 °C. Initially, the liquid crystals were extracted using toluene and were used to compare with subcritical water. The specific compounds of the liquid crystals were not identified. The liquid crystals (12 mg/g-LCD) were entirely removed from the LCD panel when treated above 300 °C by means of extraction with the subcritical water. Although liquid crystal was successfully removed, recovery was complicated due to the degradation of liquid crystals above 250 °C. A recovery of 70% was obtained at 250 °C without deformation of the molecules. Consequently, this study has shown that although it is not practical to recover LC from LCD panel waste using subcritical water, liquid crystals can be removed efficiently. This method is auspicious in reducing hazardous liquid crystal from waste LCD panel before their disposals at landfill sites
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