This study evaluated the odor mitigation effect of rice husk biochar addition to the bedded pack dairy barn floor using lab-scale reactors for five days. Rice husk biochar mixed with dairy manure and sawdust mixture at different ratios (5%-addition test unit: adding biochar by 5% of the total solid weight of the mixture, 10%-addition test unit: adding biochar by 10% of the total solid weight of the mixture). Cumulative NH3 and H2S emissions of 10%-addition test unit were reduced by 26% (p< 0.05) and 46% (p = 0.0655), respectively, compared with control. However, 5%-addition test unit did not show NH3 and H2S emission reduction. Further research is needed to determine the appropriate level of biochar addition between 5 and 10%, and to evaluate applicability in the field through economic analysis.

Preparation of advanced functional materials from agricultural waste by eco-friendly processing route is inevitable for sustainable development. This work demonstrates the development of carbon/silica (C/SiO2) and carbon/silicon carbide (C/ SiC) composite foam monoliths of low thermal conductivity, high EMI shielding performance and reasonable compressive strength from rice husk. The C/SiO2 and C/SiC composite foams are obtained by carbonization and subsequent carbothermal reduction, respectively, of rice husk–sucrose composites consolidated by filter-pressing rice husk powder dispersed in sucrose solutions of various concentrations (300–600 g L− 1). The amorphous nature of silica in C/SiO2 and the presence of β-SiC in C/SiC are evidenced from XRD and TEM analysis. The compressive strength and thermal conductivity are depending on the foam density which is tailored by sucrose solution concentration. The compressive strength in the ranges of 0.32–1.67 and 0.19–1.19 MPa are observed for C/SiO2 and C/SiC foams, respectively, with density in the ranges of 0.26–0.37 and 0.18–0.29 g cm− 3. The C/SiO2 and C/SiC exhibited thermal conductivity in the ranges of 0.150–0.205 W m− 1 K− 1 and 0.165–0.431 W m− 1 K− 1, respectively. The C/SiO2 and C/SiC composite foams show absorption dominated EMI shielding effectiveness in the ranges of 18–38.5 dB and 20–43.7 dB, respectively. The inherent pore channels and corrugated surface structure in rice husk, electrically conducting carbon and dielectric SiO2 and SiC contribute to the total EMI shielding.

Because of depletion of fossil fuel from the earth curst and increase of environmental concerns, in search of an efficient alternative to the traditional carbon black (CB), a biochar known as rice husk carbon (RHC) has been examined here as a filler material to develop the EPDM composite. In this regard, the ball milled RHC was further treated with ultrasonic wave and used with or without its surface treatment by the silane coupling agent [i.e., 3-mercaptopropyl triethoxysilane (3-MPTMS)]. Among the RHC, ultrasonic treated RHC (UHC) and silane treated UHC (USHC), the EPDM composite of USHC showed nearly similar tensile strength to that of the CB (e.g., CB: 33.88 kgf/cm2, USHC: 31.38 kgf/cm2 at 20 wt% filler loading) with an enhanced elongation at break (e.g., CB: 206%, USHC: 342% at 20 wt% filler loading) and surprisingly much less compression set value (CB: 40.87%, USHC: 18.95% even after 40 wt% of filler loading). Compared to RHC, the UHC also showed its better performance next to the USHC. In addition to presence of both the carbon and silica in RHC and additional silica within the flexible aliphatic chain in USHC, the disintegration of RHC by ultrasonic treatment towards its narrow particle distribution, smaller particle size, and increased surface area is considered very much effective to develop the corresponding high performance EPDM composites. Thus, the use of waste material, i.e., rice husk through the ultrasonication of RHC followed by its surface treatment can be used as a potential filler material to prepare the environment friendly and cost effective high performing composites to be used in different efficient end products, and motivated further for industrial upscaling.

The present work focused on the determination of texture, morphology, crystallinity, and gas adsorption characteristics of porous graphene prepared from rice husks ashes at different stabilization temperature. The stabilization temperature applied in this work is 100 °C, 200 °C, 300 °C, and 400 °C to convert rice husk into rice husk ashes (RHA). Chemical activation was adopted at temperature 800 °C using potassium hydroxide (KOH) as dehydrating agent at (1:5) impregnation ratio to convert RHA into rice husk ashes-derived graphene (GRHA). The resultant GRHA were characterized in terms of their morphological changes, SSA, crystallinity, and functional group with TEM, the BET method, Raman spectroscopy, and XRD analysis, respectively. Results from this study showed that the SSA of the GRHA at stabilization temperature 200 °C (1556.3 m2/g) is the highest compared to the other stabilization temperature. Raman spectroscopy analysis revealed that all GRHA samples possess D, G, and 2D bands, which confirm the successful synthesis of the rice husks into porous graphene-like materials, known as GRHA. Appearance of diffraction peak in XRD at 44.7° indicating the graphitic structure of all the GRHA samples. Meanwhile, the TEM images of GRHA200 exhibited wrinkled structures due to the intercalation of oxygen and a few layers of graphene flakes. These wrinkled structures and graphene layers are the other factors that lead to the highest SSA of GRHA200 compared to other prepared samples GRHA. Furthermore, the adsorption capacity of CH4 for GRHA200 is up to 43 cm3/g at 35 bar and ambient temperature, almost double the adsorption capacity performance of GRHA400 at the same operating pressure and temperature.

본 연구는 기능성 팽화 스낵의 개발을 위하여 우수한 식이섬유소원인 차전자피를 첨가한 쌀 압출성형물의 물리적 특성에 대하여 살펴보았다. 원료 배합비는 쌀을 기본 원료로 하여 차전자피의 함량(0, 7, 14, 21%)을 달리하였고, 압출성형 공정변수는 스크루 회전속도 200 rpm, 사출구 온도 140oC, 수분함량 20%로 조절하였다. 압출성형 후 직경 팽화율, 비길이, 밀도, 겉보기 탄성계수, 파괴력, 조직감, 색도, 수분용해지수, 수분흡착지수, 미세구조를 측정하였다. 직경 팽화율은 차전자피 함량이 증가할수록 감소하였으며, 비길이, 밀도, 겉보기 탄성계수와 파괴력은 증가하는 경향을 보였다. 부착성은 차전자피 함량이 증가할수록 증가하였으며 21% 첨가에서 급격히 증가하였다. 차전자피의 첨가량이 증가할수록 명도는 감소하였고 적색도, 황색도, 총 색도차는 증가하는 경향을 보였다. 수분용해지수와 수분흡착지수는 압출성형 공정 후 모두 증가하였으며 차전자피의 함량이 증가할수록 증가하였다. 미세구조는 차전자피 첨가량이 증가할수록 팽화와 기공의 크기가 감소하여 압출성형물의 밀도가 증가하였다. 결론적으로 차전자피의 첨가량이 증가할수록 팽화를 감소시켜 단단한 조직감을 나타내었고 높은 수분흡수력으로 인해 부착성이 증가하여 14% 이하로 첨가 하는 것이 바람직하다. 또한 차전자피의 함량이 높은 팽화 스낵을 개발하기 위하여 유화제의 첨가 뿐만 아니라 차전 자피의 전처리 등 추가적인 연구가 필요할 것이다.

In this study, the different effects of ultrasonic surface treatment on rice husk carbon (RHC) were studied. The RHC was treated by ultrasound in water, silane, and polyphosphoric acid. Particle size, chemical changes of the surface, dispersion, and surface area were all investigated. The ultrasonic treatment in acid increased the hydrophilicity of RHC. The ultrasonic treatment in silane produced silanol having amphiphilic property. The surface treatment of RHC in a water and acid medium with ultrasound increased the surface area and pore volume of RHC. Therefore, it is expected that the ultrasonically treated RHC as a biofiller is an effective substitute to commercial filler. This would have a positive effect both economically and environmentally.

In this study, baked rice donuts with added psyllium seed husk were manufactured and their quality and retrogradation characteristics were investigated. Control (Con) was made only with wheat flour; Psyllium seed husk in the amount of 8, 12, 16 and 20 grams was added to make rice donuts (P8, P12, P16 and P20). Higher amounts of psyllium seed husk reduced the moisture loss and baking loss, and increased the moisture content and water holding capacity of the donuts. The specific volume of Con was the highest of all the groups. As the amount of psyllium seed husk increased, the lightness and yellowness of the crumb decreased, and the redness of the crumb increased. Hardness also increased as the amount of psyllium seed husk increased. The hardness of P16 was the most similar to that of Con. The scanning electron microscopy images also identified that the structure of the donuts got denser as the amount of psyllium seed husk increased. Rate constant (k) of the rice donuts with psyllium seed husk were lower than that of Con. In conclusion, it is considered that P16 is the sample that is the most similar to Con in terms of texture, but the retrogradation was more retarded in P16 than Con.

An electroless deposition method was used to modify the surface properties of rice husk ceramic particles (RHC) by depositing nano-nickel on the surface of the RHC (Ni-RHC). The dry tribological performances of aluminum matrix composite adobes containing different contents of RHC and Ni-RHC particles have been investigated using a micro-tribometer. Results showed that the Ni–RHC particles substantially improved both the friction and wear properties of the Ni-RHC/aluminum matrix adobes. The optimal concentration was determined to be 15 wt% for both the RHC and Ni–RHC particles. The improvements in the tribological properties of aluminum adobes including the Ni-RHC were ascribed to frictioninduced peeling off of Ni coating and formation of protection layer on the wear zone, both of which led to low friction and wear volume.

Three activated carbons (ACs) were prepared using NaOH (N) as an activating agent. Hy-drofluoricacid pre-leached rice husk was used as a precursor. After leaching, the precursor was washed with distilled water, dried, crushed, and then sieved; a size fraction of 0.3-0.5 mm was selected for carbonization in the absence of air at 600°C. The carbonization prod-uct (LC) was mixed with NaOH at ratios of 1:2, 1:3, and 1:4 (wt of LC: wt of NaOH) and the produced ACs after activation at 800°C were designated NLC21, NLC31, and NLC41, respectively. Surface and textural properties were determined using nitrogen adsorption at -196°C, scanning electron microscopy images, thermogravimetric analysis, and Fourier transform infrared spectra . These ACs were used as adsorbents for lead(II) from aqueous solutions. The effects of the textural properties and the chemistry of the carbon surfaces were investigated and the impact of the operation conditions on the capacity for lead(II) sorption was also considered. Modificationof NLC41 with H2O2 and HNO3 gave two other adsorbents, HNLC41 and NNLC41 respectively. These two new samples exhibited the highest removal capacities for lead(II), i.e.117.5 and 128.2 mg/g, respectively. The adsorption data fittedthe Langmuir isotherm and the kinetic adsorption followed pseudo-second order kinet-ics. The thermodynamic parameters have been determined and they indicated a spontaneous endothermic process.

Activated carbon (AC) was synthesized from rice husks using the chemical activation method with KOH, NaOH, a combination of (NaOH + Na2CO3), and a combination of (KOH + K2CO3) as the chemical activating reagents. The activated carbon with the highest surface area (around 2000m2/g) and high porosity, which allows the absorption of a large number of ions, was applied as electrode material in electric double layer capacitors (EDLCs). The AC for EDLC electrodes is required to have a high surface area and an optimal pore size distribution; these are important to attain high specific capacitance of the EDLC electrodes. The electrodes were fabricated by compounding the rice husk activated carbons with super-P and mixed with polyvinylidene difluoride (PVDF) at a weight ratio of 83:10:7. AC electrodes and nickel foams were assembled with potassium hydroxide (KOH) solution as the electrolyte. Electrochemical measurements were carried out with a three electrode cell using 6 M KOH as electrolyte and Hg/HgO as the reference electrode. The specific capacitance strongly depends on the pore structure; the highest specific capacitance was 179 F/g, obtained for the AC with the highest specific surface area. Additionally, different activation times, levels of heating, and chemical reagents were used to compare and determine the optimal parameters for obtaining high surface area of the activated carbon.

The production of functional activated carbon materials starting from inexpensive natural precursors using environmentally friendly and economically effective processes has attracted much attention in the areas of material science and technology. In particular, the use of plant biomass to produce functional carbonaceous materials has attracted a great deal of attention in various aspects. In this study the preparation of activated carbon has been attempted from rice husks via a chemical activation-assisted microwave system. The rice husks were milled via attrition milling with aluminum balls, and then carbonized under purified N2. The operational parameters including the activation agents, chemical impregnation weight ratio of the calcined rice husk to KOH (1:1, 1:2 and 1:4), microwave power heating within irradiation time (3-5 min), and the second activation process on the adsorption capability were investigated. Experimental results were investigated using XRD, FT-IR, and SEM. It was found that the BET surface area of activated carbons irrespective of the activation agent resulted in surface area. The activated carbons prepared by microwave heating with an activation process have higher surface area and larger average pore size than those prepared by activation without microwave heating when the ratio with KOH solution was the same. The activation time using microwave heating and the chemical impregnation ratio with KOH solution were varied to determine the optimal method for obtaining high surface area activated carbon (1505 m2/g).

Dye removal from waste water via adsorption by activated carbons (ACs) developed from agricultural wastes represents an ideal alternative to other expensive treatment options. Physical and chemical ACs were prepared from rice husks. The textural properties of the ACs were characterized by Brunauer-Emmett-Teller-N2 adsorption and scanning electron microscopy. The chemistry of the carbon surface was investigated by Fourier transform infrared spectroscopy, base and acid neutralization capacities, pH of the active carbon slurry, and pHpzc. The adsorption capacities of the ACs for the basic dye (methylene blue) and acid dye (acid green 25) were determined using parameters such as contact time, pH, and temperature. NaOH-ACs showed the highest surface area and total pore volume, whereas steam-ACs showed the lowest ones.

A carbonaceous sorbent was prepared from rice husk via sulphuric acid treatment. After preparation and washing, the wet carbon with moisture content 85% was used in its wet status in this study due to its higher reactivity towards Cr(VI) than the dry carbon. The interaction of Cr(VI) and the carbon was studied and two processes were investigated in terms of kinetics and equilibrium namely Cr(VI) removal and chromium sorption. Cr(VI) removal and chromium sorption were studied at various initial pH (1.6-7), for initial Cr(VI) concentration (100 mg/l). At equilibrium, maximum Cr(VI) removal occurred at low initial pH (1.6-2) where, Cr(III) was the only available chromium species in solution. Cr(VI) removal, at such low pH, was related to the reduction to Cr(III). Maximum chromium sorption (60.5 mg/g) occurred at initial pH 2.8 and a rise in the final pH was recorded for all initial pH studied. For the kinetic experiments, approximate equilibrium was reached in 60-100 hr. Cr(VI) removal data, at initial pH 1.6-2.4, fit well pseudo first order model but did not fit pseudo second order model. At initial pH 2.6-7, Cr(VI) removal data did not fit, anymore, pseudo first order model, but fit well pseudo second order model instead. The change in the order of Cr(VI) removal process takes place in the pH range 2.4-2.6 under the experimental conditions. Other two models were tested for the kinetics of chromium sorption with the data fitting well pseudo second order model in the whole range of pH. An increase in cation exchange capacity, sorbent acidity and base neutralization capacity was recorded for the carbon sorbent after the interaction with acidified Cr(VI) indicating the oxidation processes on the carbon surface accompanying Cr(VI) reduction.

The objective of this study was to examine the torrefaction process of three lignocellulose biomasses (rice husks, coffee shell, and wood) produced in Vietnam. Three different torrefaction temperatures ranging from 200oC to 300oC and three residence times of 20, 40, and 60 min were considered. The result showed that temperature had a higher effect on torrefaction process of biomass than residence time. Based on the findings of this study, a residence of 40 min could be suggested for an effective and proper torrefaction process to recycle the agricultural biomass and wood at 300oC. The torrefied products become fuel sources which can be applied to replace with fossil fuels.

Soil-Cement is an outstanding paving material, as it is economic, easy to construct and environmental-friendly due to its usage of natural soil. However, compared to current methods of paving, soil-cement shows low strength and low resistance on cracking, so it is necessary to supplement those drawbacks by use of some admixtures. This paper attempts to take an in-depth study of material characteristics of soil-cement mixtures with rice husk ash which is discarded as waste to enhance the strength and durability of soil-cement. To figure that out, XRF analysis was performed. From the XRF analysis results of the chemical content in rice husk ash, SiO2 is contained as much as 64.85%. Though SiO2 content is major in the rice husk ash, it is less than the amount expected. It is due to incineration temperature and time away from ideal environment for maximum SiO2 content. In addition, it figured out the strength property and durability of rice husk ash added soil-cement mixture by compressive strength test. The compressive strength test of soil-cement mixtures showed the highest strength with 10% of rice husk ash added. This suggests rice husk ash has high potential as one of pozzolanic materials.

Currently, Eco-friendly construction materials are widely utilized for reducing CO2 emission in construction. Furthermore various engineering fibers are also added for improving a brittle behavior in concrete. In the paper, concrete specimens with 10% and 20% replacement ratio with RHA (Rice Husk Ash) are prepared, and engineering behaviors in RHA and OPC concrete are evaluated with different addition of coconut fiber from 0.125~0.375% of volume ratio. Several basic tests including compressive strength, tensile strength, flexural strength, impact resistance, and bond strength are performed, and crack width and deflections are also measured in flexural test. RHA is evaluated to be very effective in strength development and 0.125% of fiber addition leads significant improvement in tensile strength, ductility, and crack resistance. RHA and coconut fiber are effective construction material both for reutilization of limited resources and performance improvement in normal concrete.

This research investigated the feasibility of rice husk (RH) as a biosorbent for the removal of anions from aqueoussolution. RH-g-GMA-Am biosorbent, which possesses anionic exchangeable function, was prepared through graftpolymerization of glycidyl methacrylate (GMA) in the presence of N,N'-methylene-bis-acrylamide as a cross-linker usingpotassium peroxydisulphate as a redox initiator and subsequent amination reaction using ethylenediamine (EDA),diethylenetriamine (DETA), dimethylamine (DMA) and trimethylamine (TMA) as a amine source. Fourier transforminfrared (FTIR) and scanning electron microscopy (SEM) analysis as well as the sorption capacity for anions verifiedthe presence of grafted GMA polymers and amine groups on the RH surface. The zero point of surface potential ofaminated RH-g-GMA-Am sorbent was 6.4, which facilitated the sorption of anions on the positively charged sorbent atpH<6.4. The sorption capacity of RH-g-GMA-Am depending on the amination chemicals increased in the order:DETA≥EDA>DMA>TMA, i.e., primary amine>secondary amine>tertiary amine. The sorption selectivity of RH-g-GMA-Am sorbent aminated with DETA and EDA in the presence of equimolar anions and at pH 4.7 increased in theorder: SO4>PO4>NO3>F. Furthermore, their sorption capacities for PO4 were much higher than those of commercialanion-exchange resins. The results obtained suggest that the RH-g-GMA-Am biosorbent prepared by the GMA graftcopolymerization and subsequent amination can be used as an effective anion-exchanger comparable to commercial anion-exchange resins.