Synthesis of Hydrophilic Derivative Surfactants From Algae-Derived Unsaponifiable Lipids

In the context of decarbonizing the economy, the utilization of biologically sourced feedstocks to produce replacements for petroleum-derived materials is becoming more urgent. Improving renewable biomass production and utilization is imperative for commercializing future biorefineries. Algae-derived biomass is a particularly promising feedstock thanks to its attractive oil content and composition; specifically, the high-value products in the unsaponifiable lipids have not been included in a conversion process. Here we demonstrate surfactant synthesis from a complex oil fraction as the hydrophobic donor moieties, yielding products that are similar to commercially available surfactants such as the linear alkyl benzene sulfonates. Unsaponifiable lipids extracted from algae were derivatized to non-ionic surfactants using a green chemical synthesis route based on a double esterification with succinic acid and polyethylene glycol. The in-depth molecular and structural surfactant characterization is included and indicates that the resulting properties fall between those of pure cholesterol and phytol used as surrogates for the reaction synthesis demonstration. This is the first demonstration of an effective and potentially high-value synthesis of functional surfactants with properties that can be tailored based on the relative composition of the resulting hydrocarbon alcohol components in the mixture. This novel green chemistry synthesis approach provides a route to high-value product synthesis from algae.

Screening of Bacteria in the Biodegradation of Linear Alkyl Benzene Sulfonate (LBAS) From Car Wash Waste Water in Tehran (Iran)

Linear alkyl benzene sulfonate (LABS) is a substance used as a surfactant in anionic detergents. Today, it is the most widely used surfactant in detergent products after soap. The aim of this study was to screen effective isolates for the degradation of LABS from car wash effluents in Tehran (Iran). In this study, 10 effluent samples were randomly collected from car washes in Tehran (Iran). Isolation of mesophilic aerobic bacteria was performed by direct and pre-enrichment culture techniques. Biodegradation of sodium dodecyl sulfonate by isolates and turbidity was investigated by methylene blue active substance (MBAS) method, and the superior strain was identified by molecular method (Polymerase Chain Reaction, PCR), which approximately 86% of the material was degrade by the bacterial isolate, and the isolate was identified as Bacillus licheniformis.The results of MBAS method showed that the rate of LBAS degradation by bacteria was 86%, which indicates the high power of this bacterium to degrade LABS from sewage systems (car wash effluents). It was also shown that the concentration of LABS during 8 days of biodegradation period by this bacterium decreased from 80%, which indicates a significant decrease in LABS by Bacillus licheniformis. According to our results, Bacillus licheniformis can be used to dagrade LABS and its degradation in wastewater treatment systems of car wash effluents whose effluents are based on alkyl benzene sulfonates.

Primary, secondary screening and evaluation of LAS degrading potential of soil bacteria isolated from Vidya Pratishthan’s college area

Inefficiency of use of soap in hard water popularized the use of anionic surfactants namely, branched alkylbenzene sulphonates (BAS) and Linear alkyl benzene sulphonates (LAS) in detergents. The low cost and superior solubility in hard water had made them popular and first choice of many household care-products. However, the disadvantage associated with their use was formation of stable foam over waterbodies which is detrimental for both the aquatic plants and animals. The current study involves primary and secondary screening of LAS degrading organisms and evaluates their potential. The three isolates screened isolate 1 can degrade LAS to the tune of 66% in 5 days, isolate 2 and isolate 3 degrade 72.16% and 68.25% respectively in 4 days.

Value addition study on coker kero for producing alpha olefin and alkyl benzene

Coker kero stream is obtained from delayed coking which contains saturates with alpha olefins and PNA compounds which was physicochemical characterised. The fractions present in coker kero may be used further for value added products such as alkyl benzene and naphthalene etc. The study described potential of coker kero via aromatics and non-aromatics separation by using liquid-liquid extraction (LLE) with N-methyl pyrrolidone (NMP), acetonitrile and methanol as solvents of different polarity. Methanol imparts best colour improvement as per ASTM D-1500. Beside this, adsorption study on coker kero was performed using fuller’s earth, chalk powder, red ochre and wood-stick’s ash as adsorbents. The adsorption study suggested that fuller’s earth not only separate aromatics and non-aromatics form coker kero, but also acts as a better adsorbent than graphitic carbon (activated charcoal) and is found suitable for colour improvement comparatively. This study inferred the separation of polar components, improvement in the colour, odour and established the stable fuel. FT-IR study suggested that N-methyl Pyrrolidone gives better results comparatively other solvents. HC22 type analysis of coker kero raffinate and extract phase confirm the sharp extraction of coker kero feed using N-Methyl pyrrolidone as it is a good solvent for extraction of aromatics. GCMS and HRMS compositional analysis successfully performed for the coker kero and it is separated aromatic and non-aromatic fractions.

Kaji Eksperimen Terhadap Penggunaan Bahan Bakar Emulsi Pada Burner

The purpose of this study was to observe the combustion of diesel fuel combined with the percentage volume of water and emulsifier, namely alkyl benzene sulfonic acid (ABS). The emulsion fuel composition used in this experimental study is a mixture of diesel fuel, emulsion and water. The composition of the emulsion fuel is designed according to the percentage of water volume and the emulsifier in diesel fuel with a variation of the percentage of 10%, 20%, and 30%. The parameters observed were combustion flame temperature, combustor annulus wall temperature, hot gas temperature, air fuel ratio (AFR), heat loss, and flame shape from differences in the composition of the percentage volume of emulsion fuel. In this test using Combustion Laboratory Unit C 491. The results showed that the heat absorbed due to cooling (Qa) in the AFR stoichiometry of diesel fuel (diesel) 26.334 kW was smaller than emulsion fuel (30.096 kW), so the use of emulsion fuel on the Burner Combustion Laboratory Unit C 49 is very suitable. The shape of the flame produced by the combustion of emulsion fuel is short, turbulent, and covered in water vapor.

Visible-Light-Induced Deep Aerobic Oxidation of Alkyl Aromatics

<b>Oxidation is a major chemical process to produce oxygenated chemicals in both nature and chemical industry. Currently, industrial deep oxidation processes from polyalkyl benzene are major routes to produce benzoic acids and benzene polycarboxylic acids (BPCAs), while to some extent suffering from the energy-intensive and potentially hazardous drawbacks and the sluggish separation issues. In this report, visible-light-induced deep aerobic oxidation of (poly)alkyl benzene to benzene</b><b> (poly)carboxylic acids was developed. CeCl₃ was proved to be an efficient HAT (Hydrogen Atom Transfer)catalyst in the presence of alcohol as both hydrogen and electron shuttle. Dioxygen (O₂) was found as a sole terminal oxidant. In most cases, pure products were easily isolated by simple filtration, showing the advantages of for scaling up. The reaction provides an ideal way to form valuable fine chemicals from abundant petroleum feedstocks.</b>

Visible-Light-Induced Deep Aerobic Oxidation of Alkyl Aromatics

<b>Oxidation is a major chemical process to produce oxygenated chemicals in both nature and chemical industry. Currently, industrial deep oxidation processes from polyalkyl benzene are major routes to produce benzoic acids and benzene polycarboxylic acids (BPCAs), while to some extent suffering from the energy-intensive and potentially hazardous drawbacks and the sluggish separation issues. In this report, visible-light-induced deep aerobic oxidation of (poly)alkyl benzene to benzene</b><b> (poly)carboxylic acids was developed. CeCl₃ was proved to be an efficient HAT (Hydrogen Atom Transfer)catalyst in the presence of alcohol as both hydrogen and electron shuttle. Dioxygen (O₂) was found as a sole terminal oxidant. In most cases, pure products were easily isolated by simple filtration, showing the advantages of for scaling up. The reaction provides an ideal way to form valuable fine chemicals from abundant petroleum feedstocks.</b>