Direct and efficient liquefaction of potato peel into bio-oil

The world has become dependent on petroleum as a feedstock for most products that we use in our daily lives. As an alternative, bio-refineries that transform biomass into biofuels and primary chemicals are emerging. Actually, many wastes are not fully recycled. For instance, potato peel is a cheap residue available from the potato industry. Up to now, potato peel has been used mostly for livestock feeding. Here, potato peel waste was subjected to direct acid liquefaction at 160 °C in 2-ethylhexanol and diethylene glycol using p-toluene sulfonic acid as catalyst. The product was characterized by infrared spectroscopy, chemical analysis, hydroxyl number and acid value. Results show that liquefaction was achieved in yields higher than 80%. The reactional profile shows two time zones, one comprising the process of liquefaction and one corresponding to the process of decomposition. Kinetics indicate that the liquefaction process occurs 1.9 times faster than the decomposition process. Overall, our findings show for the first time that, despite the water content, potato peel waste can be used to produce bio-oil. The products can be further used as fuels or refined chemicals such as levulinic acid, furfural, 5-hydroxyfurfural, dimethyl furfural and sugars in fermentation processes.     

Thermal treatment of plasma-synthesized goethite improves Fenton-like degradation of orange II dye

Various iron oxides are used for Fenton reactions to degrade organic pollutants. The degradation efficiency may be improved by transforming an iron oxide phase to another. Here, we report on the transformation of goethite into hematite by thermal treatment at 400 °C. The products were analyzed by X-ray diffractometry, Raman spectroscopy, scanning electron microscopy and N₂-physisorption. The catalytic activities were measured for orange II bleaching at initial concentration of 25 mg L^?1, pH 3, catalyst concentration of 0.2 g L^?1; 5 mM H₂O₂, 30 °C. Results show that the synthesized goethite was successfully transformed into hematite, and the specific surface area of the material increased from 134 to 163 m² g^?1. The bleaching efficiency of the orange II dye reached 100 % for the hematite product, versus 78 % for goethite. Therefore, a moderate thermal treatment of a plasma-synthesized goethite improves the catalytic oxidation of organic pollutants.     

Effect of Cu-ZSM-5 catalysts with different CuO particle size on selective catalytic oxidation of N,N-Dimethylformamide

● A series of Cu-ZSM-5 catalysts were tested for DMF selective catalytic oxidation. ● Cu-6 nm samples showed the best catalytic activity and N₂ selectivity. ● Redox properties and chemisorbed oxygen impact on DMF catalytic oxidation. ● Isolated Cu²⁺ species and weak acidity have effects on the generation of N₂. N, N-Dimethylformamide (DMF), a nitrogen-containing volatile organic compound (NVOC) with high emissions from the spray industry, has attracted increasing attention. In this study, Cu-ZSM-5 catalysts with different CuO particle sizes of 3, 6, 9 and 12 nm were synthesized and tested for DMF selective catalytic oxidation. The crystal structure and physicochemical properties of the catalyst were studied by various characterization methods. The catalytic activity increases with increasing CuO particle size, and complete conversion can be achieved at 300–350 °C. The Cu-12 nm catalyst has the highest catalytic activity and can achieve complete conversion at 300 °C. The Cu-6 nm sample has the highest N₂ selectivity at lower temperatures, reaching 95% at 300 °C. The activity of the catalysts is determined by the surface CuO cluster species, the bulk CuO species and the chemisorbed surface oxygen species. The high N₂ selectivity of the catalyst is attributed to the ratio of isolated Cu²⁺ and bulk CuO species, and weak acidity is beneficial to the formation of N₂. The results in this work will provide a new design of NVOC catalytic oxidation catalysts.     

Optimization of process parameters of extraction of lotaustralin from the roots of Rhodiola rosea L using supercritical CO2 plus modifier

Lotaustralin from the root of Rhodiola rosea L was extracted using supercritical carbon dioxide with methanol as modifier. Response surface methodology using Box–Behnken experimental design was utilized to explore parameters for supercritical carbon dioxide extraction. The effects of various values of temperatures (50–70 °C), pressures (200--400 bar), and percentages of methanol modifier (80%–100%) on the extraction yields of lotaustralin were evaluated. Extract identification was performed using high-performance liquid chromatography. The experimental data obtained were fitted to second-order polynomial equations and assessed using analysis of variance. The highest yields predicted from the experiments were 2.05 g kg^?1 lotaustralin at the optimal values, i.e. temperature 65 °C, pressure 316 bar, 88% methanol modifier at a flow rate of 0.4 mL min^?1, and dynamic extraction time 90 min.     

Efficacy of woody biomass and biochar for alleviating heavy metal bioavailability in serpentine soil

Crops grown in metal-rich serpentine soils are vulnerable to phytotoxicity. In this study, Gliricidia sepium (Jacq.) biomass and woody biochar were examined as amendments on heavy metal immobilization in a serpentine soil. Woody biochar was produced by slow pyrolysis of Gliricidia sepium (Jacq.) biomass at 300 and 500 °C. A pot experiment was conducted for 6 weeks with tomato (Lycopersicon esculentum L.) at biochar application rates of 0, 22, 55 and 110 t ha^?1. The CaCl₂ and sequential extractions were adopted to assess metal bioavailability and fractionation. Six weeks after germination, plants cultivated on the control could not survive, while all the plants were grown normally on the soils amended with biochars. The most effective treatment for metal immobilization was BC500-110 as indicated by the immobilization efficiencies for Ni, Mn and Cr that were 68, 92 and 42 %, respectively, compared to the control. Biochar produced at 500 °C and at high application rates immobilized heavy metals significantly. Improvements in plant growth in biochar-amended soil were related to decreasing in metal toxicity as a consequence of metal immobilization through strong sorption due to high surface area and functional groups.     

Effect of light and temperature on the population dynamics of two toxic bloom forming Cyanobacteria – Microcystis ichthyoblabe and Anabaena aphanizomenoides

The effect of light and temperature on the growth of Microcystis ichthyoblabe and Anabaena aphanizomenoides, isolated from the subtropical Oued Mellah lake, Morocco (33°30′N–07°20′W), were investigated in batch culture. Growth rates at 66 light–temperature combinations were determined and fitted with different mathematical models. The results show that the two Cyanobacteria grow at all light intensities and temperatures, except at 10 °C for A. aphanizomenoides, where the growth was strongly limited. The μ_max of M. ichthyoblabe increased with temperature from 0.56 d^?1 at 10 °C to 1.32 d^?1 at 35 °C. At all tested temperatures, a relative photoinhibition within the studied range of irradiance was observed and the photosensitivity was thermodependent. For Anabaena, the obtained μ_max ranged between 0.07 d^?1 at 10 °C and 1.46 d^?1 at 35 °C, and a weak photoinhibition was observed at 15 °C. The positive correlation between μ_max and I_opt (r²≥0.93) indicates a close interaction between light and temperature on the cyanobacteria growth. The results obtained in this work suggest that the growth of these two species is possible under low light and low temperature.     

Characterization and performance of V2O5/CeO2 for NH3-SCR of NO at low temperatures

A series of CeO₂ supported V₂O₅ catalysts with various loadings were prepared with different calcination temperatures by the incipient impregnation. The catalysts were evaluated for low temperature selective catalytic reduction (SCR) of NO with ammonia (NH₃). The effects of O₂ and SO₂ on catalytic activity were also studied. The catalysts were characterized by specific surface areas (S_BET) and X-ray diffraction (XRD) methods. The experimental results showed that NO conversion changed significantly with the different V₂O₅ loading and calcination temperature. With the V₂O₅ loading increasing from 0 to 10 wt%, NO conversion increased significantly, but decreased at higher loading. The optimum calcination temperature was 400°C. The best catalyst yielded above 80% NO conversion in the reaction temperature range of 160°C–300°C. The formation of CeVO₄ on the surface of catalysts caused the decrease of redox ability.     

Removal of Remazol Brilliant Violet-5R dye using periwinkle shells

The purpose of this research is to obtain optimal processing conditions for the adsorption of Remazol Brilliant Violet-5R (RBV-5R) dye onto activated carbon prepared from periwinkle shells (PSAC) by chemical activation with KOH using response surface methodology. Central composite design (CCD) was used to determine the effects of three preparation variables; CO₂ activation temperature, CO₂ activation time and KOH:char impregnation ratio (IR) on two responses; percentage RBV-5R dye removal and PSAC yield. Based on the CCD, two quadratic models were developed for percentage RBV-5R dye removal and PSAC yield, respectively. The most influential factor on each experimental design response was identified from the analysis of variance (ANOVA). The optimum conditions for the adsorption of RBV-5R dye onto PSAC were CO₂ activation temperature of 811 °C, CO₂ activation time of 1.70 h and IR of 3.0, resulting in 81.28% RBV-5R dye removal and 28.18% PSAC yield. PSAC prepared under optimum conditions was mesoporous with a Brunauer–Emmett–Teller surface area of 1894 m²·g^?1, total pore volume of 1.107 cm³·g^?1 and average pore diameter of 2.32 nm. The surface morphology and functional groups of the activated carbon were respectively determined from the scanning electron microscopy and Fourier transform infrared analysis.     

Synthesis, physicochemical characterizations and catalytic performance of Pd/carbon-zeolite and Pd/carbon-CeO2 nanocatalysts used for total oxidation of xylene at low temperatures

In this work, xylene removal from waste gas streams was investigated via catalytic oxidation over Pd/carbon-zeolite and Pd/carbon-CeO₂ nanocatalysts. Activated carbon was obtained from pine cone chemically activated using ZnCl₂ and modified by H₃PO₄. Natural zeolite of clinoptilolite was modified by acid treatment with HCl, while nano-ceria was synthesized via redox method. Mixed supports of carbon-zeolite and carbonceria were prepared and palladium was dispersed over them via impregnation method. The prepared samples were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), Brunauer-Emmett-Teller surface area (BET), Fourier transform infrared spectroscopy (FTIR) and thermogravimetric (TG) techniques. Characterization of nanocatalysts revealed a good morphology with an average particle size in a nano range, and confirmed the formation of nano-ceria with an average crystallite size below 60 nm. BET analysis indicated a considerable surface area for catalysts (～1000 m²·g^?1). FTIR patterns demonstrated that the surface groups of synthesized catalysts are in good agreement with the patterns of materials applied in catalyst synthesis. The performance of catalysts was assessed in a low-pressure catalytic oxidation pilot in the temperature range of 100° C-250°C. According to the reaction data, the synthesized catalysts have been shown to be so advantageous in the removal of volatile organic compounds (VOCs), representing high catalytic performance of 98% for the abatement of xylene at 250°C. Furthermore, a reaction network is proposed for catalytic oxidation of xylene over nanocatalysts.     

Removal of cyanide in aqueous solution by oxidation with hydrogen peroxide in presence of activated alumina

This work is dedicated to the removal of free cyanide from aqueous solution by oxidation with hydrogen peroxide H₂O₂ catalyzed by neutral activated alumina. Effects of initial molar ratio [H₂O₂]₀/[CN^?]₀, catalyst amount, pH, and temperature on cyanide removal have been examined. The presence of activated alumina has increased the reaction rate showing thus, a catalytic activity. The rate of removal of cyanides increases with rising initial molar ratio [H₂O₂]₀/[CN^?]₀ but decreases at pH 10 to 12. Increasing the alumina amount from 1.0 to 30 g/L has a beneficial effect, and increasing the temperature from 20 °C to 35 °C improves cyanide removal. The kinetics of cyanide removal has been found to be of pseudo-first-order with respect to cyanide and the rate constants have been determined.     

Pd nanoparticles entrapped in TiO<Subscript>2</Subscript> nanotubes for complete butane catalytic combustion at 130 °C

Air pollution by volatile organic compounds is a major health issue due to increasing industrialization and urbanization, notably in the developing countries. Cleaning organic pollutants by catalytic combustion is a potential solution, but actual methods require relatively high temperatures, thus increasing remediation costs. There is therefore a need for methods that operate at mild temperatures. Here we prepared a novel catalyst made of Pd nanoparticles entrapped in TiO₂ nanotubes by vacuum-assisted impregnation. Then, we tested this catalyst for butane combustion. The catalyst was characterized by N₂ adsorption–desorption isotherms, transmission electronic microscopy, energy-dispersive X-ray analysis coupled with a scanning transmission electron microscope, X-ray photoelectron spectroscopy and temperature programmed oxidation. Results show a complete combustion of butane at 130 °C, which is about 20 °C lower than temperatures required by actual catalysts made of Pd nanoparticles deposited on the exterior surface of TiO₂ nanotubes. Structure characterization suggests that this higher performance at lower temperature is explained by the confinement of TiO₂ nanotubes. Such a confinement could hinder the metal sintering and, in turn, facilitate the formation of PdO during oxidation on the entrapped Pd nanoparticles.     

Temperature effects on the toxicity of four trace metals to adult spotted Babylonia snails (Babylonia areolata)

A study was conducted to determine the median lethal toxicity of four heavy metals on the marine gastropod Babylonia areolata. Median lethal toxicity tests were conducted to observe the sensitivity of this gastropod to metals and how variations in temperature might affect toxicity of test elements. Four heavy metals were used in the study. It was observed that the 96-hr LC₅₀ (in mg/L) for the different metals was found to be nickel (Ni) 33.53 (35.22–28.43), copper (Cu) 44.59 (46.43–41.53), cadmium (Cd) 21.53 (23.43–18.37), and zinc (Zn) 27.34 (28.81–24.24) at room temperature 24 °C. With temperature as a variable, median lethal concentration (LC₅₀) values were observed to increase from 22.41 mg/L at 10 °C to 27.34 mg/L at 28 °C and reduce to 18.43 mg/L at 30 °C and a further rise in toxicity was observed at 35 °C where LC₅₀ value was 12.7 mg/L as seen in the case of Zn. It was also observed that at 40 °C thermal and chemical toxicity overlapped as 100% mortality was observed in controls. This trend was noted in all metals for Babylonia areolata indicating that temperature played an important role in determining LC₅₀ values of toxicants.     

Supercritical fluid extraction of biofuels from biomass

A sustainable source of energy production can be provided using renewable resources. For instance, biomass is transformed into biofuels using several techniques such as supercritical fluid extraction, an effective thermochemical process. Here we review results on biofuels obtained from lignocellulosic and algal biomass using supercritical fluids. Biofuel yield and composition are controlled by operating conditions such as extraction temperature, pressure, biomass and solvent type, and the presence of catalysts. The extraction temperature is the major factor controlling biofuel yield. Biofuel yields can also be improved with the use of catalysts. Major compounds in biofuels from lignocellulosic biomass are phenols, catechols, guaiacols, syringols, syringaldehydes, syringyl acetone, acids, and esters. Most of these compounds are produced by lignin decomposition in lignocellulose. Furfural and derivatives are produced by the decomposition of cellulose and hemicellulose. Fatty acid alkyl esters are formed from lignin fragmentation by condensation of compounds bearing C–O or C=O. Prominent compounds in biofuels from algal biomass are saturated or unsaturated fatty acid alkyl esters.     

硫酸盐废水生物处理产生的硫化物处理含Pb2+、Zn2+的钢丝酸洗废水

在一套小型搅拌反应器中,研究了碱沉淀(KOH,处理a)、碱沉淀及硫酸盐废水厌氧处理产生的硫化物出水混合(KOH+出水混合,处理b)、碱沉淀及N2吹脱硫酸盐废水厌氧处理产生的硫化物(KOH+N2吹脱,处理c),以及碱沉淀、硫酸盐废水厌氧处理产生的硫化物出水混合和N2吹脱硫化物联合(KOH+出水混合+N2吹脱,处理d)等4组处理方式对含Zn2+、Pb2+的钢丝绳酸洗废水处理效果的影响.废水pH值为0.7,Zn2+和Pb2+含量分别为450和3274 mg.L-1.结果表明,KOH+出水混合+N2吹脱的处理方式对废水有较好的处理效果,Zn2+和Pb2+的去除为氢氧化物、硫化物沉淀的共同作用结果,处理后,废水中Zn2+和Pb2+的去除率均达99.6%以上,满足污水综合排放标准(GB 8978—1996).     

Adsorption of methylene blue onto activated carbon derived from periwinkle shells: kinetics and equilibrium studies

Periwinkle shell, an abundant and inexpensive natural resource, was used to prepare activated carbon by physicochemical activation with potassium hydroxide (KOH) and carbon dioxide (CO₂) as the activating agents at 850 °C for 2 h. The adsorption equilibrium and kinetics of methylene blue dye on such carbon were then examined at 25 °C. Adsorption isotherm of the methylene blue (MB) on the activated carbon was determined and correlated with common isotherm equations. The equilibrium data for methylene blue adsorption well fitted to the Langmuir equation, with maximum monolayer adsorption capacity of 500.00 mg/g. Two simplified kinetic models including pseudo-first-order and pseudo-second-order equation were selected to follow the adsorption processes. The adsorption of methylene blue on activated carbon derived from periwinkle shell could best be described by the pseudo-second-order equation. The kinetic parameters of this best-fit model were calculated and discussed.     

Steam activation,characterisation and adsorption studies of activated carbon from maize tassels

In this paper, steam-produced activated carbon (STAC) from maize tassel (MT) was evaluated for its ability to remove basic dye (methylene blue MB) from aqueous solution in a batch adsorption process. The equilibrium experiments were conducted in the range of 50–300 mg/L initial MB concentrations at 30°C, for effect of pH, adsorbent dosage and contact time. The experimental data were analysed by Langmuir, Freundlich and Temkin isotherm models of adsorption. Freundlich adsorption isotherm was found to have highest value of R²(R²=0.97) compared to other models of Langmuir and Temkin having (0.96 and 0.95 respectively). STAC has a high adsorptive capacity for MB dye (200 mg/g) and also showed favourable adsorption for the dye with the separation factor (R_L<1) for the dye-activated carbon system. The kinetic data obtained were analysed using pseudo first-order kinetic equation and pseudo second-order kinetic equation. The experimental data fitted well into pseudo second-order kinetic equation, as demonstrated by the high value of R².     

Chelator-induced bioextraction of heavy metals from artificially contaminated soil by mushroom (Coprinus comatus)

This study investigated the potential use of chelator-induced bioextraction of heavy metals from soil by Coprinus comatus in a pot experiment. Two production waves of the mushroom were obtained to determine biomass and metal concentration. The application of ethylenediaminetetraacetic acid (EDTA) or nitrilotriacetate (NTA) slightly inhibited the growth of C. comatus, but significantly enhanced the accumulation of heavy metals in fruiting bodies compared with the control. The highest concentrations of Pb, Cu and Cd reached 900.60, 783.61 and 23.64 mg·kg^?1 in a single pot, respectively. However, application of citric acid (CA) had no effect on metal uptake. Moreover, chelators applied to soil after fructification increased the dry biomass and metal concentration in fruiting bodies compared with those applied before sowing mycelia. EDTA was more efficient for inducing metal uptake by C. comatus than NTA or CA, and split applications of EDTA after fructification resulted in the highest total metal uptake by mushroom, i.e. 19.08±2.84, 17.57±0.69 and 0.55±0.06 mg for Pb, Cu and Cd, respectively, which were 130, 12 and 5 times values obtained with the control. Interestingly, many mushrooms turned blue after soil had been treated with chelator, indicating that these mushrooms are rich in Cu.     

Chemical deactivation of V2O5-WO3/TiO2 SCR catalyst by combined effect of potassium and chloride

V₂O₅-WO₃/TiO₂ catalyst was poisoned by impregnation with NH₄Cl, KOH and KCl solution, respectively. The catalysts were characterized by X-ray diffraction (XRD), inductively coupled plasma (ICP), N₂ physisorption, Raman, UV-vis, NH₃ adsorption, temperature-programmed reduction of hydrogen (H₂-TPR), temperature-programmed oxidation of ammonia (NH₃-TPO) and selective catalytic reduction of NO _x with ammonia (NH₃-SCR). The deactivation effects of poisoning agents follow the sequence of KCl>KOH?NH₄Cl. The addition of ammonia chloride enlarges the pore size of the titania support, and promotes the formation of highly dispersed V = O vanadyl which improves the oxidation of ammonia and the high-temperature SCR activity. K⁺ ions are suggested to interact with vanadium and tungsten species chemically, resulting in a poor redox property of catalyst. More importantly, potassium can reduce the Brønsted acidity of catalysts and decrease the stability of Brønsted acid sites significantly. The more severe deactivation of the KCl-treated catalyst can be mainly ascribed to the higher amount of potassium resided on catalyst.     

Solvent-free biodiesel epoxidation

Biodiesel emerged again recently as an alternative for fossil fuels. Besides energy, biodiesel can be used as raw material to synthesize high value products such as epoxides. Indeed, epoxides are versatile intermediates in organic synthesis for numerous reactions due to the high reactivity of the oxirane ring. Actually common epoxidation by peracids in organic solvent can last several hours according to the double bonds number. The solvent confers selectivity to the reaction, preventing di-hydroxylation. Alternatively solvent-free reactions can be done in shorter times, but hydroxylation is less controlled. Here, we set up the synthesis of epoxides from methyl and ethyl esters of waste cooking oil, without solvent or metal catalyst. We tested molar ratio of hydrogen peroxide and formic acid, double bond number, reaction time, and temperature. Results show that the highest epoxide yields and selectivity, with high conversion of the double bonds, were obtained for temperature reactions between 50 and 65 °C, reaction times from 2 to 3 h, and molar ratio of 20/2/1. For those conditions, the double bonds conversion is equal or near 100 %, with epoxide yield and selectivity between 85 and 93 %. Organic solvent suppression, besides being environmentally friendly, also saves reaction time and subsequent purification steps.     

Platinum in PM2.5 of the metropolitan area of Mexico City

The increase in platinum (Pt) in the airborne particulate matter with size ≤2.5 µm (PM_2.5) in urban environments may be interpreted as result of the abrasion and deterioration of automobile catalyst. Nowadays, about four million vehicles in Mexico City use catalytic converters, which means that their impact should be considered. In order to evaluate the contribution of Pt to environmental pollution of the metropolitan area of Mexico City (MAMC), airborne PM_2.5 was collected at five different sites in the urban area (NW, NE, C, SW, SE) in 2011 during April (dry-warm season), August (rainy season) and December (dry-cold season). Analytical determinations were carried out using a ICP-MS with a collision cell and kinetic energy discrimination. The analytical and instrument performance was evaluated with standard road dust reference material (BCR-723). Median Pt concentration in the analyzed particulate was is 38.4 pg m^?3 (minimal value 1 pg m^?3 maximal value 79 pg m^?3). Obtained Pt concentrations are higher than those reported for other urban areas. Spatial variation shows that SW had Pt concentration significantly higher than NW and C only. Seasonal variation shows that Pt median was higher in rainy season than in both dry seasons. A comparison of these results with previously reported data of PM₁₀ from 1991 and 2003 in the same studied area shows a worrying increase in the concentration of Pt in the air environment of MAMC.