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Towards natural care products : Structural and deposition studies of bio-based polymer and surfactant mixtures

Del Giudice, Alessandra (author)
Sapienza University of Rome,Sapienza Univ Rome, Ple A Moro 5, I-00185 Rome, Italy
Gubitosi, Marta (author)
CR Competence AB, POB 124, SE-22100 Lund, Sweden
Sthoer, Adrien (author)
CR Competence AB, POB 124, SE-22100 Lund, Sweden
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Köhler, Sebastian (author)
Lund University,Lunds universitet,LINXS - Institute of advanced Neutron and X-ray Science,Kemiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH,Lund Univ, Div Phys Chem, POB 124, SE-22100 Lund, Sweden
Ayscough, Sophie (author)
Lund University,Lunds universitet,Fysikalisk kemi,Enheten för fysikalisk och teoretisk kemi,Kemiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Physical Chemistry,Physical and theoretical chemistry,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH,Lund Univ, Div Phys Chem, POB 124, SE-22100 Lund, Sweden
Skoda, Maximilian W.A. (author)
ISIS Neutron and Muon Source,ISIS Neutron & Muon Source, Harwell Sci & Innovat Campus, Didcot OX110QX, England
Nylander, Tommy (author)
Lund University,Lunds universitet,NanoLund: Centre for Nanoscience,Annan verksamhet, LTH,Lunds Tekniska Högskola,Fysikalisk kemi,Enheten för fysikalisk och teoretisk kemi,Kemiska institutionen,Institutioner vid LTH,LINXS - Institute of advanced Neutron and X-ray Science,LTH profilområde: Nanovetenskap och halvledarteknologi,LTH profilområden,LU profilområde: Ljus och material,Lunds universitets profilområden,Other operations, LTH,Faculty of Engineering, LTH,Physical Chemistry,Physical and theoretical chemistry,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH,Faculty of Engineering, LTH,LTH Profile Area: Nanoscience and Semiconductor Technology,LTH Profile areas,Faculty of Engineering, LTH,LU Profile Area: Light and Materials,Lund University Profile areas,Sungkyunkwan University,LINXS Inst Adv Neutron & X Ray Sci, Lund, Sweden; Lund Univ, Div Phys Chem, POB 124, SE-22100 Lund, Sweden; Lund Univ, NanoLund, Lund, Sweden; Sungkyunkwan Univ, Sch Chem Engn, Suwon 16419, South Korea; Sungkyunkwan Univ, Translat Nanobiosci Res Ctr, Suwon 16419, South Korea
Halthur, Tobias (author)
Malmö universitet,Malmö University,Institutionen för biomedicinsk vetenskap (BMV),Biofilms Research Center for Biointerfaces,CR Competence AB, POB 124, SE-22100 Lund, Sweden
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 (creator_code:org_t)
Elsevier, 2024
2024
English.
In: Colloids and Surfaces A: Physicochemical and Engineering Aspects. - : Elsevier. - 0927-7757 .- 1873-4359. ; 698
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Oppositely charged polymer-surfactant systems are expected to interact with formation of coacervate complexes near composition of charge-neutrality. Such behaviour is widely used in formulated products (e.g. household and personal care), where the co-deposition of coacervates and active ingredients on various surfaces is triggered by dilution. A transition towards the use of more sustainable ingredients is currently ongoing as a response to the need of more environmentally conscious choices in production, albeit slowed down by the often more complex and not fully understood bulk and interfacial behaviour of new ingredients. In this work, mixtures of a medium-chain fatty acid (sodium decanoate) and two grades of bio-based cationic modified inulin were studied. The phase behaviour was determined in a wide composition matrix. The formation of coacervate complexes was observed for the mixture with the higher charge density polymer at a surfactant concentration of 1–3 wt%, close to the surfactant critical micellar concentration in pure water. Such behaviour was confirmed by DLS and SAXS data, suggesting surfactant-polymer complexation in a concentrated phase of packed micelles with a micelle-to-micelle distance of ∼4.5 nm. In situ ellipsometry and neutron reflectometry experiments were conducted to study the effect on surface deposition when diluting. The ellipsometry showed an adsorbed mass of ∼1.3–1.9 mg/m2, consistent with the deposition of a coacervate layer, and considerably higher than the neat, adsorbed polymer layer of ∼0.3 mg/m2. In the case of the neutron reflectometry experiments, dilution was performed before contact with the surface (pre-mixing), and no adsorption of coacervates was observed, but rather the adsorption of a polymer layer (0.49–0.85 mg/m2). The different results obtained with the different techniques highlight the kinetic nature of bulk coacervate formation and deposition, and the competition between these two phenomena. Maximal deposition can be achieved if one can control this time window either by tuning the composition of the system or the experimental set-up, to mimic the conditions of a specific application.

Subject headings

NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)

Keyword

Biopolymers
Bulk characterisation
Coacervates
Deposition
Fatty acids
Surfactants
Surfactants

Publication and Content Type

art (subject category)
ref (subject category)

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