Search results for " Surfactants"

showing 10 items of 37 documents

Glycolipid Biosurfactant Production from Waste Cooking Oils by Yeast: Review of Substrates, Producers and Products

2021

Biosurfactants are a microbially synthesized alternative to synthetic surfactants, one of the most important bulk chemicals. Some yeast species are proven to be exceptional biosurfactant producers, while others are emerging producers. A set of factors affects the type, amount, and properties of the biosurfactant produced, as well as the environmental impact and costs of biosurfactant’s production. Exploring waste cooking oil as a substrate for biosurfactants’ production serves as an effective cost-cutting strategy, yet it has some limitations. This review explores the existing knowledge on utilizing waste cooking oil as a feedstock to produce glycolipid biosurfactants by yeast. The review f…

0106 biological sciences0301 basic medicineTP500-660Cooking oilChemistryCommodity chemicalsFermentation industries. Beverages. Alcoholcircular economyPlant Sciencemicrobial surfactantsSubstrate (biology)Raw materialPulp and paper industry01 natural sciencesBiochemistry Genetics and Molecular Biology (miscellaneous)Yeastwaste valorization03 medical and health sciences030104 developmental biologyGlycolipidused cooking oil010608 biotechnologynonconventional yeastsFood ScienceFermentation
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Supramolecular Aggregates in Vacuum: Positively Mono-Charged Sodium Alkanesulfonate Clusters

2010

The formation and structural features of positively mono-charged aggregates of sodium bis(2-ethylhexyl) sulfosuccinate (AOT) and sodium methane—(MetS), butane—(ButS) and octane—(OctS) sulfonate molecules in the gas phase have been investigated by electrospray ionization mass spectrometry, energy-resolved mass spectrometry and density functional theory (DFT) calculations. The experimental results show that the center-of-mass collision energy required to dissociate 50% of these mono-charged aggregates scantly depends on the length of the alkyl chain as well as on the aggregation number. This, together with the large predominance of mono-charged species in the mass spectra, was rationalized i…

AlkanesulfonatesSpectrometry Mass Electrospray IonizationAmphiphilic moleculeVacuumChemistryElectrospray ionizationSodiumSodiumSupramolecular chemistrychemistry.chemical_elementGeneral MedicineAtomic and Molecular Physics and Opticschemistry.chemical_compoundSulfonateTandem Mass SpectrometrySupramolecular aggregates amphiphilic molecules surfactants reversed micelles ESI MS ESI MS/MS energy resolved mass spectrometry DFT calculationsQuantum TheoryOrganic chemistrySpectroscopyEuropean Journal of Mass Spectrometry
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Solubilization of an Organic Solute in Aqueous Solutions of Unimeric Block Copolymers and Their Mixtures with Monomeric Surfactant: Volume, Surface T…

2008

The ability of aqueous systems, formed by unimeric copolymers and their mixtures with a monomeric surfactant, in solubilizing large quantities of 1-nitropropane (PrNO2) was explored. The copolymers are F68 and L64, which differ for the hydrophilicity, and the surfactant is sodium dodecanoate. For a better understanding of the mechanism of solubilization, thermodynamic (volume and differential scanning calorimetry), spectroscopy (steady-state fluorescence), viscosity, and interfacial investigations were carried out. PrNO2 causes the micellization of the unimeric copolymer, and the required amount of PrNO2 depends on the composition, the copolymer nature, and the temperature. Large quantities…

Aqueous solutionISOTHERMAL TITRATION CALORIMETRYChemistryMICELLAR SYSTEMSDYNAMIC LIGHT-SCATTERINGIONIC SURFACTANTSTRIBLOCK COPOLYMERSMicelleFluorescence spectroscopySurfaces Coatings and FilmsSurface tensionViscosityDifferential scanning calorimetryAGGREGATION BEHAVIORPulmonary surfactantChemical engineeringMIXED MICELLESPolymer chemistryMaterials ChemistryCopolymerPhysical and Theoretical ChemistrySODIUM DODECYL-SULFATEOXIDE)(13)-(PROPYLENE OXIDE)(30)-(ETHYLENE OXIDE)(13)GEMINI SURFACTANTS
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Micellization properties of cardanol as a renewable co-surfactant

2015

With the aim to improve the features of surfactant solutions in terms of sustainability and renewability we propose the use of hydrogenated natural and sustainable plant-derived cardanol as an additive to com- mercial surfactants. In the present study we demonstrated that its addition, in amounts as high as 10%, to commercial surfactants of different charge does not significantly affect surfactant properties. Conversely, the presence of hydrogenated cardanol can strongly affect spectrophotometric determination of CMC if preferential interactions with the dyes used take place. This latter evidence may be profitably exploited in surfactant manufacturing by considering that the concurrent pres…

Dynamic Laser Light Scattering.Sustainable surfactantIONIC SURFACTANTSTETRADECYLDIMETHYLAMINE OXIDEBiochemistryCardanolSurface-Active AgentsPhenolsPulmonary surfactantMoleculeOrganic chemistryFLUORESCENCEPhysical and Theoretical ChemistryMicellesCardanolCetrimoniumChemistrybusiness.industry-PotentialOrganic ChemistryWaterHYDROGENATED CARDANOLOrange OTTensiometryRenewable energyAGGREGATION NUMBERPREMICELLAR AGGREGATIONCetrimonium CompoundsSpectrophotometric determination of CMCGEMINI SURFACTANTSbusinessBEHAVIOROrganic & Biomolecular Chemistry
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Green Synthesis, Molecular Characterization and Associative Behavior of Some Gemini Surfactants without a Spacer Group.

2013

A series of new gemini surfactants without a spacer group, disodium 2,3-dialkyl-1,2,3,4-butanetetracarboxylates, were synthesized in a green chemistry context minimizing the use of organic solvents and applying microwaves (MW) when activation energy was required. Once the desired architecture was confirmed by means of the nuclear magnetic resonance technique (1H-NMR, 1H-1H COSY) for all the studied surfactants, the critical micellization concentration was determined by conductance measurements. The diffusion coefficient of micelles formed by the four compounds was characterized using pulsed field gradient (PFG)-NMR. Diffusion coefficients were found to be dependent on the concentration and …

Green chemistrygemini surfactantsmicrowavecritical micelle concentrationDiffusionContext (language use)cosmetic detergentlcsh:TechnologyMicelleArticlegreen synthesigemini surfactants green synthesis microwave cosmetic detergents critical micelle concentration PFG-NMR diffusion coefficientOrganic chemistryMoleculeGeneral Materials Sciencediffusion coefficientlcsh:MicroscopyAlkyllcsh:QC120-168.85Settore CHIM/02 - Chimica Fisicachemistry.chemical_classificationgemini surfactantcosmetic detergentslcsh:QH201-278.5lcsh:TChemistrygreen synthesisChemical engineeringlcsh:TA1-2040Critical micelle concentrationPFG-NMRlcsh:Descriptive and experimental mechanicslcsh:Electrical engineering. Electronics. Nuclear engineeringlcsh:Engineering (General). Civil engineering (General)Pulsed field gradientlcsh:TK1-9971gemini surfactants; green synthesis; microwave; cosmetic detergents; critical micelle concentration; PFG-NMR; diffusion coefficientMaterials (Basel, Switzerland)
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NEW INSIGHTS ON SUPRAMOLECULAR AGGREGATES OF SODIUM DOCUSATE (AOTNa) BY ION MOBILITY MASS SPECTROMETRY

2013

Backgorund: The ability of some surfactants to form charged aggregates in gas phase has been proven experimentally by electrospray ionization (ESI) spectrometry [1- 5]. However, in the early investigations, interesting questions concerning the structural organization of these aggregates in gas phase and if they reflect their typical self-assembling in the starting liquid solutions were not addressed. Subsequently, independently of their aggregation motive in liquid phase and of the charge state in the gas phase, some hints suggesting that surfactant molecules are organized in gas phase as reverse micelle-like aggregates have been reported Objective: The supramolecular charged aggregates for…

Ion Mobility Surfactants micelles cross sectionSettore CHIM/01 - Chimica AnaliticaSettore CHIM/06 - Chimica OrganicaSettore CHIM/08 - Chimica FarmaceuticaSettore CHIM/02 - Chimica Fisica
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Pulmonary surfactant protein C containing lipid films at the air-water interface as a model for the surface of lung alveoli.

1995

The pulmonary surfactant lines as a complex monolayer of lipids and proteins the alveolar epithelial surface. The monolayer dynamically adapts the surface tension of this interface to the varying surface areas during inhalation and exhalation. Its presence in the alveoli is thus a prerequisite for a proper lung function. The lipid moiety represents about 90% of the surfactant and contains mainly dipalmitoylphosphatidylcholine (DPPC) and phosphatidylglycerol (PG). The surfactant proteins involved in the surface tension adaption are called SP-A, SP-B and SP-C. The aim of the present investigation is to analyse the properties of monolayer films made from pure SP-C and from mixtures of DPPC, DP…

LangmuirChemical PhenomenaSurface PropertiesProteolipidsLipid BilayersMolecular Sequence DataBiophysicsPalmitic AcidsBiophysical PhenomenaSurface tensionchemistry.chemical_compoundPulmonary surfactantEllipsometryMonolayerHumansPulmonary surfactant-associated protein CAmino Acid SequenceMolecular BiologyPhospholipidsPhosphatidylglycerolChemistryChemistry PhysicalAirtechnology industry and agricultureWaterMembranes ArtificialPulmonary SurfactantsCell BiologyLipid MetabolismLipidsPulmonary AlveoliCrystallographyChemical engineeringDipalmitoylphosphatidylcholinelipids (amino acids peptides and proteins)Protein BindingMolecular membrane biology
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Palmitoylation of Pulmonary Surfactant Protein SP-C Is Critical for Its Functional Cooperation with SP-B to Sustain Compression/Expansion Dynamics in…

2010

AbstractRecent data suggest that a functional cooperation between surfactant proteins SP-B and SP-C may be required to sustain a proper compression-expansion dynamics in the presence of physiological proportions of cholesterol. SP-C is a dually palmitoylated polypeptide of 4.2 kDa, but the role of acylation in SP-C activity is not completely understood. In this work we have compared the behavior of native palmitoylated SP-C and recombinant nonpalmitoylated versions of SP-C produced in bacteria to get a detailed insight into the importance of the palmitic chains to optimize interfacial performance of cholesterol-containing surfactant films. We found that palmitoylation of SP-C is not essenti…

LipoylationSus scrofaBiophysicsAcute respiratory distressModels Biologicallaw.inventionAcylationchemistry.chemical_compoundPalmitoylationPulmonary surfactantlawAnimalsPulmonary Surfactant-Associated Protein BChemistryCholesterolMembraneTemperaturePulmonary SurfactantsBiofísicaPulmonary Surfactant-Associated Protein CBiomechanical PhenomenaCholesterolBiochemistryBiophysicsRecombinant DNAlipids (amino acids peptides and proteins)AdsorptionProteïnes
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Inhaled Surfactant in the treatment of accidental Talc Powder inhalation: a new case report

2011

Abstract The use of talcum powder is incorrectly part of the traditional care of infants. Its acute aspiration is a very dangerous condition in childhood. Although the use of baby powder has been discouraged from many authors and the reports of its accidental inhalation have been ever more rare, sometimes new cases with several fatalities have been reported. We report on a patient in which accidental inhalation of baby powder induced severe respiratory difficulties. We also point out the benefits of surfactant administration. Surfactant contributed to the rapid improvement of the medical and radiological condition, preventing severe early and late complications and avoiding invasive approac…

Lung Diseasesmedicine.medical_specialtymedicine.medical_treatmentTreatment outcomeCase Reportmacromolecular substancesTalcSettore MED/38 - Pediatria Generale E SpecialisticaPulmonary surfactantAdministration InhalationSurfactantmedicineHumansTalcum powderRespiratory physiotherapyIntensive care medicinePhospholipidsBiological ProductsInhalationRespiratory distressbusiness.industrylcsh:RJ1-570InfantRespiratory Physiotherapylcsh:PediatricsPulmonary SurfactantsBronchopulmonary LavageAccidental InhalationAnti-Bacterial AgentsBronchodilator AgentsRadiographyTreatment OutcomeCoughBaby powderTalcRespiratory DistressAccidentalDrug Therapy CombinationFemaleInhaled surfactant talc powder inhalationPowdersbusinessmedicine.drugItalian Journal of Pediatrics
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How Low Can You Go? Low Densities of Poly(ethylene glycol) Surfactants Attract Stealth Proteins.

2018

It is now well-established that the surface chemistry and “stealth” surface functionalities such as poly(ethylene glycol) (PEG) chains of nanocarriers play an important role to decrease unspecific protein adsorption of opsonizing proteins, to increase the enrichment of specific stealth proteins, and to prolong the circulation times of the nanocarriers. At the same time, PEG chains are used to provide colloidal stability for the nanoparticles. However, it is not clear how the chain length and density influence the unspecific and specific protein adsorption keeping at the same time the stability of the nanoparticles in a biological environment. Therefore, this study aims at characterizing the…

Magnetic Resonance SpectroscopyPolymers and PlasticsNanoparticleBioengineeringProtein Corona02 engineering and technology010402 general chemistry01 natural sciencesPolyethylene Glycolsnanocarriers; poly(ethylene glycol); protein corona; stealth effect; surfactantsBiomaterialschemistry.chemical_compoundColloidMicePlasmaSurface-Active AgentsAdsorptionPEG ratioMaterials ChemistryAnimalsHumansColloidsChemistrySodium Dodecyl Sulfate021001 nanoscience & nanotechnology0104 chemical sciencesClusterinRAW 264.7 CellsChemical engineeringNanoparticlesPolystyrenesProtein CoronaAdsorptionNanocarriers0210 nano-technologyEthylene glycolBiotechnologyProtein adsorptionMacromolecular bioscience
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