Extrication of biodiesel feedstock from early stage of food waste liquefaction

Biodiesel is commonly produced from vegetable oils, mostly edible and more expensive than petroleum diesel. By considering the cost of the conversion processes, cheap feedstock such as triglycerides and fatty acids (FA) extracted from early stage of food waste liquefaction has become a better choice than vegetable oils, as it could provide high yield of biodiesel without any compromise to food supply and other resources. In this study, FA from early stage of food waste liquefaction was extracted and tested for use as feedstock for biodiesel synthesis. The raw material was not pretreated but extraction was done by dry and wet methods. It was found that wet method could minimized the lost of short and medium-chained FA as well as reducing the number of steps required, thus, yielding higher amount of FA as feedstock. The effects of mixing, methanol ratio, reaction time and catalyst content were investigated for the acid-catalyzed esterification. The maximum biodiesel conversion obtained was 97.4 %.     

Gaseous ethylbenzene removal by photocatalytic TiO2 nanoparticles immobilized on glass fiber tissue under real conditions: evaluation of reactive oxygen species contribution to the photocatalytic process

Environmental Science and Pollution Research - Photocatalytic oxidation (PCO) using a TiO2 catalyst is an effective technique to remove gaseous volatile organic compounds (VOCs). Herein, a...     

Spectroscopic studies and biological evaluation of some transition metal complexes of a novel Schiff base ligands derived from 5-arylazo-salicyladehyde and o-amino phenol

Synthesis and characterization of Cu(II), Ni(II), and Zn(II) Schiff bases complexes resulted from the condensation of salicylaldehyde derivatives with o-amino phenol were discussed using elemental analysis (carbon, hydrogen, and nitrogen), molar conductance, magnetic measurements, mass spectra, and electronic spectra. The essential bands of infrared, ¹HNMR, and UV-Vis spectra as well as thermogravimetric analysis corresponding to the active groups within the three ligands and their complexes were interpreted. The dehydration and decomposition processes of the [Cu(H₂L₁)(H₂O)](OAc)₂, [Ni(H₂L₁)(H₂O)]SO₄ · H₂O, [Zn(H₂L₁)(H₂O)]SO₄ · H₂O, [Cu(H₂L₂)(H₂O)](OAc)₂, [Ni(H₂L₂)(H₂O)]SO₄ · H₂O, [Zn(H₂L₂)(H₂O)]SO₄ · 2H₂O, [Cu(H₂L₃)(H₂O)](OAc)₂ · H₂O, [Ni(H₂L₃)(H₂O)]SO₄ · 2H₂O, [Zn(H₂L₃)(H₂O)]SO₄ complexes were studied thermodynamically using the integral method applying the Coats–Redfern and Horowitz–Metzger equations and the thermodynamic parameters were calculated. It was found from the elemental analysis and the thermal studies, that the ligand behaves as tridentate ligand forming chelates with 1 : 1 (metal : ligand) stoichiometrically. The molar conductance measurements of the complexes in dimethyl sulfoxide solvent indicate that the complexes have an electrolytic nature. The biological activities of the three ligands in comparison with metal(II) complexes were studied against different Gram positive and Gram negative bacteria.     

Trace element concentration levels in three bird species in Hormod Protected Area,Larestan, Iran

The objective of the present study was to investigate the levels of Cd, Pb, Co, and Cu, in A. chukar, A. griseogularis, and Columba livia, in order to (1) examine the age- and gender-related variation in trace metal accumulation and (2) to determine the significance between metal concentrations in the kidney, liver, and pectoral muscle. Mean concentrations of Cd and Pb in the kidney of A. chukar, A. griseogularis, and C. livia were 3.7, 4.1, and 3.9?µg/g and 15.9, 13.6, and 15.5?µg/g, respectively. In the liver, they were 4.8, 4.3, and 3.9?µg/g and 21.4, 21.3, and 21.1?µg/g, and in the pectoral muscle, 2.3, 2.3, and 2.2?µg/g and 7.1, 7.1, and 7.8?µg/g, respectively. Metal concentrations in three bird species were decreased in the sequence of liver?>?kidney?>?pectoral muscle. Trace metal concentrations in the three species were higher in females than in males. The mean concentrations of Cd in the kidney and liver were higher than the background levels, as well as Pb concentrations in the liver were higher than the toxic level.     

Modified dehydrogenase enzyme assay for evaluation of the influence of Hg,Cd, and Zn on the bacterial community structure of a wastewater treatment plant

In this study, a traditional assay was modified to evaluate the effect of Hg, Cd, and Zn on the bacterial community of a sequencing batch reactor and activated sludge plants and heavy metal-resistant bacterial species were determined. After the isolation of metal-resistant bacteria, their 16S rRNA gene fragments were sequenced. The BLAST program was used to compare the resulting 16S rRNA sequences with those in GenBank database to identify the isolated bacterial species. Hg was found to be the most toxic metal for both bacterial communities investigated. Sequence batch reactor bacteria were comparatively more resistant to Hg, Cd, and Zn than those from activated sludge. The resistant strains were close to the members of genus Pseudomonas, Kocuria, Stenotrophomonas, Enterococcus, and Staphylococcus. The modified dehydrogenase enzyme assay seems to be simple, robust, and competent for evaluation of the impact of metals on bacterial activity. Sequencing batch reactor systems should be preferred over activated sludge when wastewaters containing hazardous metals are to be treated.     

固态反应法制备FeHY催化剂及其催化降解活性艳蓝的性能研究

分别以NaY、NH4Y和HY沸石为载体,以乙酰丙酮铁为铁源,采用固态反应法制备了铁负载量均为10%（w）的FeNaY-10、FeNH4Y-10和FeHY-10催化剂。考察了各催化剂对活性艳蓝（KN-R）的降解效果,其中FeHY-10的催化降解效果最佳。采用XRD和FTIR技术对FeHY-10催化剂进行表征。表征结果显示,FeHY催化剂晶体结构仍然保持了Y分子筛特有的孔道结构,铁物种在Y 分子筛表面高度分散。催化降解实验表明,催化降解KN-R的最佳工艺条件为KN-R溶液（质量浓度为300 mg/L）加入量为50 mL、溶液pH为2、催化剂FeHY-25（铁负载量为25%（w））加入量为0.281 3 g、H2O2质量浓度为6.356 g/L、降解温度为35 ℃、降解时间为140 min,在此工艺条件下FeHY催化剂对KN-R的降解率为97.4%。     

Effect of vehicle exhaust on the quantity of polycyclic aromatic hydrocarbons (PAHs) in soil

PAHs are formed during the incomplete combustion of organic substances containing carbon and hydrogen and are one of the first atmospheric pollutants identified as carcinogens. Most of the PAH environmental burden is found in the soil (95%). Soil samples collected from different roadsides were analyzed for seven polycyclic aromatic hydrocarbons (PAHs). The quantitative and qualitative analysis was carried out by UV Spectrophotometer. The individual PAH value ranged from 0.1 to 18.0 mg/kg. Phenenthrene and Pyrene were found to be the most abundant compounds. Vehicle emissions are the principal source of PAH in the Roadside soils. The highest concentration was found at site S2 (Hasthtnagri Roadside) which shows the highest traffic density.     

Radon level and radon effective dose rate determination using SSNTDs In Sannur cave, Eastern desert of Egypt

The European eel’s swimbladder nematode, Anguillicola crassus, sampled from the Asi River (Orontes River) in Antakya (Hatay, Turkey) in May 2006 were analysed by Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES) for their some heavy metal (Cd, Cr, Cu, Fe, Hg, Mn, Pb and Zn) levels. The metal concentrations of the parasites were compared to different organs (swimbladder, liver, muscle and skin) of the fish hosts. The parasite contained statistically highly significantly amounts of Fe (P < 0.05). The iron level of nematode was up to 25.52 times than the muscle of its host, Anguilla anguilla. However, bioconcentration of Cd, Cr, Cu, Hg, Mn, Pb, Zn were detected in the A. crassus and it contained no statistically differences with the other tissues of its host, the eel (P > 0.05). Furthermore, no significant differences were detected in the heavy metal accumulations between the parasitized and un-parasitized fish tissues. The analysed metals (Cd, Cr, Cu, Fe, Mn, Pb and Zn) were found in fish muscle at mean concentrations under the permissible limits proposed by FAO.     

Sorption of 17β-estradiol to pig slurry separates and soil in the soil-slurry environment

Contamination of freshwater by estrogens from manure applied to agricultural land is of grave concern because of the potentially harmful effects on aquatic life and human health. Recent developments in liquid manure (slurry) management include partial removal of particulate slurry dry matter (PSDM) by separation technologies, which may also remove parts of the estrogens and enhance infiltration of the slurry on field application and hence the interaction between estrogens and the soil matrix. This study investigated how 17β-estradiol (E2), a natural estrogen commonly found in pig manure, sorbs to agricultural soils, to different size fractions of pig slurry separates, and to soils amended with each size fraction to simulate conditions in the soil-slurry environment. A crude fiber fraction (SS1) was prepared by sieving (<500 μm) the solids removed by an on-farm separation process. Three other size fractions (SS2 > SS3 > SS4) were prepared from the liquid fraction of the separated slurry by sedimentation and centrifugation. Sorption experiments were conducted in 0.01 mol L(-1) CaCl(2) and in natural pig urine matrix. Sorption in 0.01 mol L(-1) CaCl(2) was higher than that in pig urine for all solids used. Sorption of E2 to soil increased with its organic carbon content for both liquid phases. The solid-liquid partition coefficients of slurry separates were 10 to 30 times higher than those of soils, but the organoic carbon normalized partition coefficient values, reflecting sorption per unit organic carbon, were lower for slurry separates. Mixing slurry separates with soil increased the sorption of E2 to the solid phase significantly in the order: SS1 < SS3 < SS2 for both liquid phases. In contrast, SS4 reduced the sorption of E2 to the solid phase by increasing the sorption to suspended or dissolved organic matter. The study suggested that potentially 50 to 75% of E2 in slurry can be removed from the liquid fraction of slurry by physical separation.