Abstract:This study employed HZSM‐5 (SiO2/Al2O3 = 280 mol/mol) to produce hydrocarbons from reagent‐grade isopropanol and mixed alcohols made from lignocellulosic biomass (waste office paper and chicken manure) using the MixAlco™ process. All studies were performed at P = 5000 kPa (abs). The experiments were conducted in two sets: (1) vary temperature (300–450°C) at weight hourly space velocity (WHSV) = 1.92 h−1, and (2) vary WHSV (1.92–11.52 h−1) at T = 370°C. For isopropanol at higher temperatures, the olefins underg… Show more
“…Although there was not much difference in the distillation results, the gasoline obtained at 410 °C was slightly heavier than the others. As aforementioned, there were more aromatics in the gasoline obtained at higher temperatures, and these are heavier than isomers of paraffins and olefins [11]. Figure 4 shows the distillation curves for EX1, EX4, EX7, compared to high-grade commercial gasoline.…”
Section: Resultsmentioning
confidence: 91%
“…Table 2 shows that the octane number is greater than 95 for all cases which is higher to the highest gasoline available in Ecuador with octane number 92. On the other hand, Reid vapor pressure increased with temperature because the amount of aromatics increases with temperature (which show higher vapor pressures than olefins and paraffins) in the gasoline at greater temperatures [4,11]. The cupper metal corrosion essay was negative in the three experimental runs because the hydrocarbons obtained from ethanol do not contain sulfur or acid corrosion-generating compounds.…”
Dehydration and oligomerization of ethanol to hydrocarbons was studied using a packed-bed reactor over HZSM-5 (SiO2/Al2O3=280 mol/mol) zeolite as catalyst. Nine experiments were performed at different temperature and weight hourly space velocity (WHSV) conditions. The experiments were conducted in three levels for both variables (T: 300, 350, and 410 °C) and (WHSV: 1.3, 3.7, and 7.9 h–1). For all the experiments, ethanol was dehydrated to ethylene; however, oligomerization only occurred at WHSV=1.3 h-1, where the yields to liquid hydrocarbons were 15, 25, and 10% at 300, 350, and 410 °C, respectively. The liquid hydrocarbon products were analyzed by copper metal corrosion, gum content, octane number, Reid vapor pressure, gas chromatography, and fractional distillation. The octane number was about 95 in all cases, higher than Ecuador premium gasoline octane number (92). These laboratory-scale findings provide good insights on the ethanol-to-gasoline approach that could be scaled up to the industry.
“…Although there was not much difference in the distillation results, the gasoline obtained at 410 °C was slightly heavier than the others. As aforementioned, there were more aromatics in the gasoline obtained at higher temperatures, and these are heavier than isomers of paraffins and olefins [11]. Figure 4 shows the distillation curves for EX1, EX4, EX7, compared to high-grade commercial gasoline.…”
Section: Resultsmentioning
confidence: 91%
“…Table 2 shows that the octane number is greater than 95 for all cases which is higher to the highest gasoline available in Ecuador with octane number 92. On the other hand, Reid vapor pressure increased with temperature because the amount of aromatics increases with temperature (which show higher vapor pressures than olefins and paraffins) in the gasoline at greater temperatures [4,11]. The cupper metal corrosion essay was negative in the three experimental runs because the hydrocarbons obtained from ethanol do not contain sulfur or acid corrosion-generating compounds.…”
Dehydration and oligomerization of ethanol to hydrocarbons was studied using a packed-bed reactor over HZSM-5 (SiO2/Al2O3=280 mol/mol) zeolite as catalyst. Nine experiments were performed at different temperature and weight hourly space velocity (WHSV) conditions. The experiments were conducted in three levels for both variables (T: 300, 350, and 410 °C) and (WHSV: 1.3, 3.7, and 7.9 h–1). For all the experiments, ethanol was dehydrated to ethylene; however, oligomerization only occurred at WHSV=1.3 h-1, where the yields to liquid hydrocarbons were 15, 25, and 10% at 300, 350, and 410 °C, respectively. The liquid hydrocarbon products were analyzed by copper metal corrosion, gum content, octane number, Reid vapor pressure, gas chromatography, and fractional distillation. The octane number was about 95 in all cases, higher than Ecuador premium gasoline octane number (92). These laboratory-scale findings provide good insights on the ethanol-to-gasoline approach that could be scaled up to the industry.
“…The ACN was 8.43±1.4 (305°C) and 8.24 ±1.2 (415°C). This Gaussian distribution of products was not observed in the isopropanol and mixed-alcohol reactions [ 17 , 18 ]. Fig 7 also shows the most abundant compound for each carbon number.…”
Section: Resultsmentioning
confidence: 97%
“…Although mixed alcohols and mixed ketones products have the same carbon distribution, their reaction mechanisms are very different. The purpose of this study is to extend the previous work on mixed alcohols to hydrocarbons [ 17 , 18 ] and investigate the transformation of acetone and mixed ketones to hydrocarbons. This paper also provides an insight into the reaction conditions and the type and distribution of hydrocarbons products obtained, as well as a proposed reaction mechanism.…”
In this study, two different feeds were treated to produce hydrocarbons: (1) reagent-grade acetone, and (2) mixed ketones obtained from lignocellulosic biomass via the carboxylate platform. Acetone and mixed ketones underwent catalytic self-condensation over HZSM-5. For acetone, HZSM-5(80) was used, and the experiments were conducted in two sets: (1) vary temperature (305–415°C) at P = 101 kPa (abs) and weight hourly space velocity (WHSV) = 1.3 h–1; (2) vary WHSV (1.3–7.9 h–1) at T = 350 and 415°C, and P = 101 kPa (abs). For acetone over HZSM-5(280), the experiments were conducted in two sets: (1) vary WHSV (1.3–6.5 h–1) at T = 415°C, and P = 101 kPa (abs); and (2) vary WHSV (1.3–11.8 h–1) at P = 790 kPa (abs) and T = 415°C. For mixed ketones, HZSM-5(280) was used at WHSV = 1.9 h–1, T = 430–590°C, and P = 101 kPa (abs). For acetone at higher temperatures, the conversion was 100% and the liquid products were aromatics centered on C8. At low temperatures, conversion was less and the carbon liquid distribution was centered on C9 (mainly mesitylene). For mixed ketones, catalyst deactivation was higher causing product concentrations to change over time, and the highest conversion reached was 40%.
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