Study of the influence of dilute acid pre-treatment conditions on glucose recovery from Moringa oleifera Lam for fuel-ethanol production

The influence of temperature (175 to 195°C), residence time (5 to 15 min), and sulfuric acid concentration in high (2 to 4% w/w) and low (0.5 to 1.5% w/w) levels in dilute acid pretreatment of Moringa oleifera Lam is studied. Glucose recoveries in the liquid fraction and in the hydrolyzed insoluble fraction as well as the presence of inhibitors in the liquid fraction are determined. Best experimental results are achieved at 185°C, 2% w/w acid concentration, and 5 min reaction time obtaining a glucose recovery of 83.68%. An increment in 48.81% in glucose yield compared with the one of not pretreated Moringa is obtained. 0.13 g ethanol/g Moringa from fermentation of pre-hydrolysate and hydrolysate obtained at the optimal pre-treatment conditions are obtained.     

Enzymatic hydrolysis of banana stems (Musa acuminata): Optimization of process parameters and inhibition characterization

In current work, an optimum solid loading (solid: liquid = 1:20), pH (4.8), temperature (50°C), and enzyme dosing of 20 filter paper unit (amount of enzyme required to release 1 µmol of glucose as reducing sugar from filter paper in per mL per minute) were enumerated for enzymatic hydrolysis of banana stem using cellulase from Trichoderma reesei. Further, inhibition study on enzymatic hydrolysis of banana stem was investigated by the supplementation of monosaccharides (glucose, galactose, mannose, xylose, and arabinose), disaccharide (cellobiose), and inhibitors (acetic acid and furfural obtained from pre-enzymatic hydrolysis steps). Glucose and cellobiose showed inhibitory effect on enzymatic hydrolysis of pretreated banana stem at or above 8 g/L while galactose, mannose, and xylose showed a significant inhibitory effect at or above 4 g/L. Instead of inhibition, arabinose enhanced the enzymatic hydrolysis with increase in total reducing sugars. Acetic acid did not show any significant inhibition while furfural inhibited the system at a comparative low concentration of 2 g/L. Further, scanning electron microscopy analysis was performed to investigate the difference in ultra-structural morphology of raw biomass, pretreated biomass, and biomass obtained after enzymatic hydrolysis.     

Assessment of different carbon and salinity level on growth kinetics,lipid, and starch composition of Chlorella vulgaris SAG 211-12

ABSTRACT

The quality of microalgal biofuel depends on the fatty acid (FA) distribution. A high ratio of saturated fatty acids (SFAs) favors better biofuel characteristics. Palmitic acid (C16:0) and stearic acid (C18:0) are essential FAs for required biodiesel quality. In this study, combined effects of growth medium concentrations of NaCl, glucose and glycerol on cell composition and FA profile of the Chlorella vulgaris SAG 211–12 were investigated. A central composite design (CCD) based design of experiments (DoE) was used for experimental setup. According to experimental results, the maximum mass fraction for palmitic acid (C16:0), 40.67% of total fatty acids, was obtained in the medium supplemented with 0.9% (w/v) NaCl, 0.3% (w/v) glucose, and 0.3% (w/v) glycerol, whereas stearic acid (C18:0) percentage reached the highest value of 22.16% of total fatty acids in the presence of 2.5% NaCl, 0.6% glucose, and 0.6% glycerol. According to the same set of designed experiments, best starch content was found as 22.08% of dry cell weight in a medium containing 2.0% NaCl, 0.3% glucose, and 0.3% glycerol. C16:0 mass fraction as a function of three medium ingredient concentrations was modeled using a Kriging model. Optimum concentrations of NaCl, glucose and glycerol to reach maximum C16:0 fraction were predicted as 0.5, 1, and 1%, respectively.     

Ethanol production from alkali-pretreated oil palm empty fruit bunch by simultaneous saccharification and fermentation with mucor indicus

Oil palm empty fruit bunch (OPEFB) is a potential raw material for production of lignocellulosic bioethanol. The OPEFB was pretreated with 8% sodium hydroxide (NaOH) solution at 100°C for 10 to 90 min. Enzymatic digestion was carried out using cellulase and β-glucosidase at 45°C for 24 h. It was then inoculated with Mucor indicus spores suspension and fermented under anaerobic conditions at 37°C for 96 h. Sodium hydroxide pretreatment effectively removed 51–57% of lignin in the OPEFB and also its hemicellulose (40–84%). The highest glucan digestibility (0.75 g/g theoretical glucose) was achieved in 40-min NaOH pretreatment. Fermentation by M. indicus resulted in 68.4% of the theoretical ethanol yield, while glycerol (16.2–83.2 mg/g), succinic acid (0–0.4 mg/g), and acetic acid (0–0.9 mg/g) were its by-products. According to these results, 11.75 million tons of dry OPEFB in Indonesia can be converted into 1.5 billion liters of ethanol per year.     

Evaporative Cooling of Water in a Small Vessel Under Varying Ambient Humidity

Evaporative cooling of water in a small porous clay vessel was studied under controlled humidity conditions. In steady-state experiments performed at an ambient temperature of 23 °C, the cooling effect increased from 4.7 to 8.3 °C as the ambient relative humidity decreased from 60 to 15%. External heat and mass transfer coefficients, estimated from the steady-state measurements, were used in mathematical models to predict the experimentally observed transient temperature variation of the water under ramp changes of the ambient relative humidity. With a prototypical cool chamber containing water tested in Kolkata, India under an ambient temperature of 34.5–35 °C, the cooling effect reached a maximum of 7 °C between 3 and 3:30 PM and then declined to 4.5 °C around 6 PM.     

Heat transfer of vapor chamber with different types of microchannels

Two 40-mm × 35-mm × 1.525-mm micro vapor chambers were fabricated by inductively coupled plasma etching on silicon substrates and tested in this study. One vapor chamber exhibited convergent microchannels, whose widest and narrowest width were 0.3 mm and 0.1 mm, respectively, and the other exhibited discontinuous microchannels having width of 0.3 mm. Those micro vapor chambers that were filled with deionized water in a filling ratio of approximately 48% were tested with various titled angles and input powers. The results showed that the thermal performance of the vapor chamber having discontinuous microchannels was inferior because the spacing between microchannelend and the micropostin both condensing and evaporating sections was too far to return the condensed fluid from condensing section to the evaporating section of the vapor chamber. On the contrary, the convergent microchannel in the other vapor chamber enhanced capillary force, so that the condensed liquid could be successfully forced from the condensing section to the evaporating section even with top heating mode (–90°). The thermal resistance of the vapor chamber having convergent micro channels with top heating mode was 2.08°C/W at 22 W, while the thermal resistance of the vapor chamber with horizontal heating mode was 1.46°C/W at 28 W.     

Investigation of amine amino acid salts for carbon dioxide absorption

The carbon dioxide capture potential of amine amino acid salts (AAAS), formed by mixing equinormal amounts of amino acids; e.g. glycine, β-alanine and sarcosine, with an organic base; 3-(methylamino)propylamine (MAPA), was assessed by comparison with monoethanolamine (MEA), and with amino acid salt (AAS) from amino acid neutralized with an inorganic base; potassium hydroxide (KOH). Carbon dioxide absorption and desorption experiments were carried out on the solvent systems at 40 °C and 80 °C respectively. Experimental results showed that amine amino acid salts have similar CO₂ absorption properties to MEA of the same concentration. They also showed good signs of stability during the experiments. Amino acid salt from an inorganic base, KOH, showed lower performance in CO₂ absorption than the amine amino acid salts (AAAS) mainly due to a lower equilibrium temperature sensitivity. AAAS showed better performance than MEA of same concentration. AAAS from neutralization of sarcosine with MAPA showed the best performance and the performance could be further enhanced when promoted with excess MAPA. The solvent comparison is semi-quantitative since the bubble structure, and thus gas–liquid interfacial area may not be the same for all experiments, however superficial gas velocities were kept constant.     

Biodiesel synthesis and characterization using welted thistle plant (Carduus acanthoides) as source of new non-edible seed oil

In this work we applied base catalyzed transesterification to convert non-edible welted thistle oil (Carduus acanthoides) as new non-edible feedstock into biodiesel (Fatty acid methyl esters). The highest biodiesel yield of 88% was obtained using optimized reaction conditions of 70°C and 5:1 molar ratio (methanol:oil). The synthesized esters were characterize and confirmed by the application of NMR and FT-IR techniques. Gas chromatography and mass spectroscopy identified different fatty acids as palmatic acid (C16:0), oleic acid (C18:1), linoleic acid (18:2), arachidic acid (C20:0), eicosanic acid (C20:1), and erucic acid (C22:1) in the oil of welted thistle. Six corresponding methyl esters reported in welted thistle oil biodiesel includes 9-hexadecenoic acid, hexadecanoic acid, 9-octadecadienoic acid, 11-eicosanoic acid, eicosanoic acid and 13-docosenoicacid. Fuel properties, such as density @40°C Kg/L (0.8470), kinematic viscosity @ 40°C c St (4.37), flash point (95°C), cloud point (+4°C), pour point (?5°C), and sulfur contents (0.0112% wt) of the biodiesel produced were compatible with American Society for Testing and Materials D 6751 specifications.     

Renewable biofuel production from hydrocracking of soybean biodiesel with a commercial petroleum Ni-W catalyst

As a potential hydrocarbon production method, the hydrocracking of soybean biodiesel, using a commercial petroleum hydrocracking catalyst, was studied. Experiments were carried out in a 1,000 mL, high-pressure autoclave for 2–4 hr over the temperature range of 200–280°C under an initial hydrogen pressure of 10 MPa. Hydrocracking of soybean biodiesel produced n-paraffins in the C₈–C₁₇ boiling range, which includes both green gasoline and diesel. Both pressure and temperature play important roles in the transformation of soybean biodiesel. Hydrocarbons can be formed above 220°C with a liquid yield of 81.76%. The n-alkanes content of the liquid product reached 32.29% at 280°C, with 88.32% C₁₁–C₁₄ selectivity. In addition, hydrocracking results in many changes of catalyst such as physical properties, morphology, etc. For the used catalyst, the concentrations of Ni and C increased, and the pore channels were significantly reduced.     

Carbon dioxide capture and recovery by means of TSA and/or VSA

Experimental work is performed with a 5A zeolite on a small laboratory column with heating from the wall. Carbon dioxide adsorption occurs at atmospheric pressure and different CO₂ concentrations in nitrogen. Comparisons of different methods of desorption by heating, purge and/or vacuum are studied. Desorption by heating only leads to almost pure CO₂ (around 99% purity) and a recovery nearly linear to the heating temperature, ranging from 45% at 130 °C to 79% at 210 °C. Recovery can be subsequently increased with a nitrogen purge to more than 98% but the recovered carbon dioxide is diluted due to the dispersive character of the desorption wave and the operation time is long. Increasing the flow rate decreases the desorption time but has no effect on the purity because the total purge volume remains about the same. Substitution of the purge step with a vacuum step leads to pure CO₂ and almost total recovery. Desorption under vacuum only without heating leads to pure CO₂ (around 99% purity) but limited recovery (85% in the present work).Desorption under vacuum seems to be more simple for large-scale applications. When using a water liquid ring pump, the temperature of the ring must be kept as low as possible to provide a high operating capacity.     

Pyrolysis of cellulose under catalysis of SAPO-34, ZSM-5, and Y zeolite via the Py-GC/MS method

Bio-oil from pyrolysis of biomass is an important renewable source for liquid fuel and/or for chemicals. However, the application of bio-oil was severely restricted due to its high viscosity, acidity, and low heating value. Hence, it is necessary to upgrade the bio-oil for deoxygenation or for chemicals by catalytic reactions. In this paper, the catalytic behaviors of SAPO-34, ZSM-5, and Y zeolite on pyrolysis of cellulose were investigated via pyrolyzer combined with gas chromatography and mass spectrometer (Py-GC/MS) method in Py-mode. The results showed that ZSM-5 and Y zeolite could promote the conversions of oxygen-containing components to gases, water, aromatics, and phenols. Comparatively, more gas and water were generated under the catalysis of Y zeolite at lower temperatures, while at temperatures above 700°C, the effect of ZSM-5 became more distinct; aromatics were more generated under the catalysis of ZSM-5, while Y zeolite exerted a more distinct role in promoting the formation of phenols. The effect of SAPO-34 caused more water and furfural derivatives, less aromatics and phenols, and exerted a weak influence on gases.     

INACTIVATION OF GIARDIA MURIS CYSTS BY CHLORAMINES1

ABSTRACT: In a study to measure the efficacy of chioramines at inactivating Giardia cysts, the ability of cysts to excyst was measured after exposure to different concentrations of chloramines, for different times, and at different temperatures and pH. The chloramines were generated by mixing ammonium sulfate and sodium hypochlorate in water to approximate a 7:1 chlorine:ammonia ratio by weight. Times of 40, 80, 180, and 270 minutes; temperatures of 3, 10, and 18°C; target chioramine concentrations of 0.4, 1.4, 2.0, and 2.6 mg/L; and pH of 7.0 and 8.5 were the actual values tested. The combinations of these variables that were able to inactivate >99.8 percent of the cysts were a minimum chloramine concentration of 2.26 mg/L applied for 270 minutes at a water temperature of 10°C; and at 18°C, averaged minimum chloramine concentrations of 2.14 and 1.55 mg/L applied for 180 and 270 minutes, respectively. The minimum CT values corresponding to these combinations capable of >99.8 percent cyst inactivation, are 610 at 10°C and 385 at 18°C. Temperature was noted to exert a major effect on the ability of chloramines to inactivate cysts. Modifications of the methods used to generate chloramines may have an effect on the capacity of this disinfectant to inactivate cysts.     

Investigation of activated carbon/ethanol for low temperature adsorption cooling

Commercially available adsorption cooling systems use water/silica gel, water/zeolite and ammonia/ chloride salts working pairs. The water-based pairs are limited to work above 0°C due to the water high freezing temperature, while ammonia has the disadvantage of being toxic. Ethanol is a promising refrigerant due to its low freezing point (161 K), nontoxicity, zero ozone depletion, and low global warming potential. Activated carbon (AC) is a porous material with high degree of porosity (500–3000 m²/g) that has been used in wide range of applications. Using Dynamic Vapour Sorption (DVS) test facility, this work characterizes the ethanol adsorption of eleven commercially available activated carbon materials for cooling at low temperature of ?15°C. DVS adsorption results show that Maxsorb has the best performance in terms of ethanol uptake and adsorption kinetics compared to the other tested materials. The Maxsorb/ethanol adsorption process has been numerically modeled using computational fluid dynamics (CFD) and simulation results are validated using the DVS experimental measurements. The validated CFD simulation of the adsorption process is used to predict the effects of adsorbent layer thickness and packing density on cycle uptake for evaporating temperature of ?15°C. Simulation results show that as the thickness of the Maxsorb adsorbent layer increases, its uptake decreases. As for the packing density, the amount of ethanol adsorbed per plate increases with the packing density reaching maximum at 750 kg/m³. This work shows the potential of using Maxsorb/ethanol in producing low temperature cooling down to ?15°C with specific cooling energy reaching 400 kJ/kg.     

Performance of a small-scale solar-powered adsorption cooling system

In this study, an experimental investigation on the performance of a small-scale residential-size solar-driven adsorption (silica gel-water) cooling system that was constructed at Assiut University campus, Egypt is carried out. As Assiut area is considered as hot, arid climate, field tests for performance assessment of the system operation during the summer season are performed under different environmental operating conditions. The system consists of an evacuated tube with a reflective concentration parabolic surface solar-collector field with a total area of 36 m², a silica gel-water adsorption chiller of 8 kW nominal cooling capacity, and hot and cold water thermal storage tanks of 1.8 and 1.2 m³ in volume, respectively. The results of summer season field test show that under daily solar insolation varying from 21 to 27 MJ/m², the solar collectors employed in the system had high and almost constant thermal efficiency. The daily solar-collector efficiency during the period of system operation ranged from about 50% to 78%. The adsorption chiller performance shows that the chiller average daily coefficient of performance (COP) was 0.41 with the average cooling capacity of 4.4 kW when the cooling-water and chilled-water temperatures were about 31°C and 19°C, respectively. As the chiller cooling water is cooled by the cooling tower in the hot arid area, the cooling water is at a higher temperature than the design point of the chiller. Therefore, an experiment was carried out using the city water for cooling. The results show that an enhancement in the chiller COP by 40% and the chilling power by 17% has been achieved when the city water was 27.7°C.     

Pyrolysis of commingled waste textile fibers in a batch reactor: Analysis of the pyrolysis gases and solid product

The main object of this study was the investigation of the thermal recycling of commingled waste textile fibers, with the aim of the production of useful end products. Differential scanning calorimetry/Thermo gravimetric analysis (DSC/TGA) was applied to determine the thermal degradation characteristics of the commingled waste textile fibers and there are two peaks located at the temperature ranges of 299–360°C and 399–500°C. Commingled waste fiber was pyrolyzed in a nitrogen atmosphere in relation to three different temperatures (500, 600, and 700°C), heating rates (25 and 50°C min^?1), and retention times (15 and 30 min). The effect of the experimental conditions such as pyrolysis temperature, heating rates, and retention time on the formation of char and gas--liquid products was investigated and the product yields were determined from the rate of the weight loss. The highest conversion rate 82.9 wt.% liquid--gas product and 17.1 wt.% char product was achieved at 700°C. Pyrolysis gases were taken for every 7, 15, and 25 min and were analyzed for major components such as CO, CO₂, CH₄, and H₂ by gas chromatography. The pyrolysis char called as carbon black derived from the pyrolysis of commingled waste textile fibers was analyzed for a range of properties, including the elemental analysis, moisture content, ash content, calorific value, and trace metal analysis.     

Relationship between liquid depth and the acoustic generation of hydrogen: design aspect for large cavitational reactors with special focus on the role of the wave attenuation

Understanding the effect of the liquid depth (z) on the acoustic generation of hydrogen is highly required for designing large-scale sonoreactors for hydrogen production because acoustic cavitation is the central event that initiates sonochemical reactions. In this paper, we present a computational analysis of the liquid-depth effect on the generation of H₂ from a reactive acoustic bubble trapped in water irradiated with an attenuating sinusoidal ultrasound wave. The computations were made for different operating conditions of frequency (355–1000 kHz), acoustic intensity (1–5 W/cm²), and liquid temperature (10–30°C). The contribution of the acoustic wave attenuation on the overall effect of depth was appreciated for the different conditions. It was found that the acoustic generation of hydrogen diminished hardly with increasing depth up to z = 8 m, and the depth effect was strongly operating parameter-dependent. The sound wave attenuation played a crucial role in quenching H₂ yield, particularly at higher z. The reduction of the H₂ yield with depth was more pronounced at higher frequency (1000 kHz) and lower temperature (10°C) and acoustic intensity (1 W/cm²). The attenuation of the sound wave may contribute up to 100% in the overall reductive effect of depth toward H₂ production rate. This parameter could be imperatively included when studying all aspects of underwater acoustic cavitation.     

迪那2气田液化气无水冷却工艺研究

迪那2气田液化气生产设计采用空冷加水冷工艺,存在能耗大和水冷器易腐蚀结垢等安全隐患。利用HYSYS软件对迪那2气田轻烃回收工艺进行分析,并增设液化气后冷器,利用脱乙烷塔气相对液化气进行冷却,通过醇烃液分离压力、后冷器及空冷器冷却能力等参数的模拟计算和优化,将醇烃液三相分离器压力由常规的2.5MPa提高至5MPa,取消醇烃液导热油加热和液化气水冷,降低了装置能耗,年节水1.44×104m3,节电1.45×105 kW.h,杜绝了水冷器腐蚀穿孔的安全隐患,最终提出了醇烃液高压分离+空冷器+后冷器的液化气无水冷却工艺。     

The effect of pyrolysis atmosphere on bio-oil yields and structure

A food industry waste, almond shell, was pyrolyzed under three different environment static, nitrogen, and steam to produce bio-oil and its derivatives. The oil yield obtained at pyrolysis temperature of 600°C was 24.23% in a static atmosphere, whereas it increased to 27.25% and 33.05% in nitrogen and steam atmospheres, respectively. The bio-oil obtained under steam atmosphere is very efficient due to the production of high liquid and gas yields. Moreover, co-feeding steam during the pyrolysis altered the bio-oil structure by increasing the aliphatics and reducing the asphaltenes. Moreover, steam treatment also increases H/C and heating value of bio-oils. According to the obtained results, steam pyrolysis is an alternative option for future applications in refineries.     

The Evaluation of Mesoporous Materials as Catalyst in Fast Pyrolysis of Wheat Straw

In this study, wheat straw was chosen as a biomass sample and the fast pyrolysis of this sample was carried out with or without catalyst at different conditions in a well-swept fixed-bed reactor. Experiments were carried out in a well-swept tubular fixed-bed reactor with a heating rate of 300°C/min, between pyrolysis temperature ranges 300–800°C in the nitrogen atmosphere. The results indicated that a maximum oil yield of 31.9% was obtained at a pyrolysis temperature of 500°C in non-catalytic procedure. Siliceous and Al-MCM-41 materials were evaluated as potential catalysts in the pyrolysis experiments. Mesoporous materials have large pore dimensions with strong acid sites. These acidic sites catalyze some reactions in pyrolysis. The product yields and the quality of bio-oil were influenced with using MCM-41 materials. The bio-oil yield was reduced, whereas the gas yield increased with using a catalyst in the experiments. An increase in the fractions of pure phenol, alkyl phenols, alkenes+alkanes, carbonyls, aromatic, and cyclic compounds and a decrease in the fractions of methoxy phenols, acids+esters, furans, and alcohols were observed in the presence of Al-MCM-41 material. According to all results, the use of Al-MCM-41 materials as catalyst in the pyrolysis can be suggested to obtain both quality fuels and valuable chemicals.     

Scleropyrum pentandrum (Dennst.) mabb—oil as a feedstock for biodiesel production—engine performance and emission studies

A feasibility study on utilization of non edible oil of Scleropyrum pentandrum was carried out to see its potential as a new source for biodiesel production. Nonedible oil seeds of Scleropyrum pentandrum have oil content of 55–60%. Transesterification of freshly extracted oil in the presence of anhydrous sodium hydroxide at a concentration 1% (w/v oil) and methanol-oil ratio of 40% (v/v oil) yields 90.8% methyl esters under conventional heating. Month old oil requires sulfuric acid pretreatment (esterification) before transesterification. The transesterified oil has a density 889–893 kg/m³; kinematic viscosity of 4.21–5.7 mm²/s; cetane index 46.03; pour point of ?15°C and gross calorific value of 40.135 MJ/kg and oxidative stability of 2.35 hours. The properties are well within the Indian, European and American standard limits recommended for biodiesel except the oxidation stability, which can be improved by adding antioxidant additives. The engine performance studies of B10 and B20 blends of Scleropyrum pentandrum biodiesel (SP biodiesel) with statistical inference confirmed that it can be used as a fuel in CI engines without any engine modifications. The engine exhaust emission analysis showed that the emission of hydrocarbons can be minimized by at least 15–20%, CO emission by 15%, smoke opacity by 10–12% and moderately lesser CO₂ and NOx emissions.