Without appropriate treatment, lignocellulosic biomass is not suitable to be fed into existing combustion systems because of its high moisture content, low bulk energy density and difficulties in transport, handling and storage. The aim of this study was to investigate the effects of torrefaction treatment on the weight loss and energy properties of fast growing species in Malaysia (Acacia spp., and Macaranga spp.) as well as oil palm biomass (oil palm trunk and empty fruit bunch). The lignocellulosic biomass was torrefied at three different temperatures 200, 250 and 300 °C for 15, 30 and 45 min. Response surface methodology was used for optimization of torrefaction conditions, so that biofuel of high energy density, maximized energy properties and minimum weight loss could be manufactured. The analyses showed that increase in heating values was affected by treatment severity (cumulated effect of temperature and time). Our results clearly demonstrated an increased degradation of the material due to the combined effects of temperature and treatment time. While the reaction time had less impact on the energy density of torrefied biomass, the effect of reaction temperature was considerably stronger under the torrefaction conditions used in this study. It was demonstrated that each biomass type had its own unique set of operating conditions to achieve the same product quality. The optimized torrefaction conditions were verified empirically and applicability of the model was confirmed. The torrefied biomass occurred more suitable than raw biomass in terms of calorific value, physical and chemical properties. The results of this study could be used as a guide for the production of high energy density solid biofuel from lignocellulosic biomass available in Malaysia.
In the present study, agricultural biomass—palm kernel shell (PKS) and coconut shell (CS)—was used to produce high porosity bioadsorbent using two-stage continuous physical activation method with different gas carrier (air and N2) in each stage. The activation temperature was set constant at 600, 700, 800 or 900°C for both activation stages with the heating rate of 3°C min−1. Two parameters, the gas carrier and activation temperature, were determined as the significant factors on the adsorption properties of bioadsorbent. BET, SEM, FTIR, TGA, CHNS/O and ash content were used to elucidate the developed bioadsorbent prepared from PKS and CS and its capacity towards the adsorption of methylene blue and iodine. The novel process of two-stage continuous physical activation method was able to expose mesopores and micropores that were previously covered/clogged in nature, and simultaneously create new pores. The synthesized bioadsorbents showed that the surface area (PKS: 456.47 m2 g−1, CS: 479.17 m2 g−1), pore size (PKS: 0.63 nm, CS: 0.62 nm) and pore volume (PKS: 0.13 cm3 g−1, CS: 0.15 cm3 g−1) were significantly higher than that of non-treated bioadsorbent. The surface morphology of the raw materials and synthesized bioadsorbent were accessed by SEM. Furthermore, the novel process meets the recent industrial adsorbent requirements such as low activation temperature, high fixed carbon content, high yield, high adsorption properties and high surface area, which are the key factors for large-scale production of bioadsorbent and its usage.
Latex production from Hevea brasiliensis rubber tree is the second most important commodity in Malaysia, but this industry is threatened by the white root rot disease (WRD) caused by Rigidoporus microporus that leads to considerable latex yield loss and tree death. This study aimed to characterize and compare the virulence of five R. microporus isolates obtained from infected rubber trees located at different states in Malaysia. These isolates were subjected to morphological and molecular characterization for species confirmation and pathogenicity test for the determination of virulence level. BLAST search showed that the ITS sequences of all the pathogen isolates were 99% identical to R. microporus isolate SEG (accession number: MG199553) from Malaysia. The pathogenicity test of R. microporus isolates conducted in a nursery with 24 seedlings per isolate showed that isolate RL21 from Sarawak has developed the most severe above- and below-ground symptoms of WRD on the rubber clone RRIM600 as host. Six months after being infected with R. microporus, RL21 was evaluated with the highest average of disease severity index of 80.52% for above- and below-ground symptoms, followed by RL22 (68.65%), RL20 (66.04%), RL26 (54.38%), and RL25 (43.13%). The in vitro growth condition tests showed that isolate RL21 of R. microporus has optimum growth at 25–30 °C, with the preference of weakly acidic to neutral environments (pH 6–7). This study revealed that different virulence levels are possessed among different R. microporus isolates even though they were isolated from the same host species under the same climate region. Taken together, field evaluation through visual observation and laboratory assays have led to screening of the most virulent isolate. Determination of the most virulent isolate in the present study is vital and shall be taken into consideration for the selection of suitable pathogen isolate in the development of more effective control measures in combating tenacious R. microporus.
White root disease caused by Rigidoporus microporus is the most devastating disease in majority of the rubber growing countries, including Malaysia. This study aimed to screen and decipher the mechanisms involved in the biocontrol agents responsible for the inhibition of R. microporus. Among 16 fungal isolates, Trichoderma spp. showed promising results with the highest percent of inhibition shown by Trichoderma asperellum (80.54%). Scanning electron microscopy study revealed coiling of hyphae by Trichoderma species against R. microporus. T. asperellum has demonstrated a maximum inhibition in both volatile and non-volatile metabolite tests with its 75% culture filtrate on PDA plate was observed to cause abnormal morphological character in R. microporus. All Trichoderma species were shown to produce hydrolytic enzymes (chitinase, cellulase and β-1,3-glucanase) and they were active siderophore producers. Present study demonstrated the possible mechanisms involved and responsible for successful inhibition of R. microporus under in vitro condition especially by T. asperellum.
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