TY - JOUR A1 - Lopez, Carlos G. A1 - Manova, Anna A1 - Hoppe, Corinna A1 - Dreja, Michael A1 - Schmiedel, Peter A1 - Job, Mareile A1 - Richtering, Walter A1 - Böker, Alexander A1 - Tsarkova, Larisa A. T1 - Combined UV-Vis-absorbance and reflectance spectroscopy study of dye transfer kinetics in aqueous mixtures of surfactants JF - Colloids and surfaces : an international journal devoted to the principles and applications of colloid and interface science ; A, Physicochemical and engineering aspects N2 - We report an analytical approach to study the competitive processes of solubilisation in micelles and of adsorption onto hydrophobic surfaces of poorly soluble hydrophobic dyes. The method is demonstrated on model systems containing two sources of Disperse Red 60: a bulk powder and a donor red textile, with molecularly dissolved dye stabilised in an aqueous environment by mixed micelles of anionic and non-ionic surfactants. The process of dye transfer between a donor textile (red polyester), surfactant micelles and an acceptor textile (white polyamide) was quantified by a combination of colorimetric analyses. UV-Vis absorbance was used to follow the extraction of the dye and to evaluate the solubilisation capacity of the micellar solution. A calibration curve for textile reflectance versus the adsorbed dye was generated to quantify the mass of dye transferred onto the acceptor textile. A combination of both techniques allowed us to compare the amount of dye desorbed from the donor textile and adsorbed onto the acceptor textile as a function of time for systems undergoing exhaustion-solubilisation mechanisms and only solubilisation mechanism. Up to similar or equal to 10 min of the washing process, the released dye is predominantly solubilised in surfactant micelles. At later times, the adsorption of the dye on the hydrophobic surface is energetically favoured. The shift of the desorption equilibrium in the presence of the acceptor textile results in similar or equal to 30% increase in the release of the dye. The reported methodology provides direct comparative analysis between the solubilisation capacity of amphiphilic stabilisers and the tendency of the dye to adsorb on solid substrates, important for designing novel concepts of disperse dye solubilisation and dye transfer inhibition during textile washing. KW - Dye transfer KW - Disperse dyes KW - Surfactants KW - Detergent KW - Colorimetric analysis KW - Washing fastness Y1 - 2018 U6 - https://doi.org/10.1016/j.colsurfa.2018.04.024 SN - 0927-7757 SN - 1873-4359 VL - 550 SP - 74 EP - 81 PB - Elsevier CY - Amsterdam ER - TY - JOUR A1 - Kyriakos, Konstantinos A1 - Philipp, Martine A1 - Adelsberger, Joseph A1 - Jaksch, Sebastian A1 - Berezkin, Anatoly V. A1 - Lugo, Dersy M. A1 - Richtering, Walter A1 - Grillo, Isabelle A1 - Miasnikova, Anna A1 - Laschewsky, André A1 - Müller-Buschbaum, Peter A1 - Papadakis, Christine M. T1 - Cononsolvency of water/methanol mixtures for PNIPAM and PS-b-PNIPAM: pathway of aggregate formation investigated using time-resolved SANS JF - Macromolecules : a publication of the American Chemical Society N2 - We investigate the cononsolvency effect of poly(N-isopropylacrylamide) (PNIPAM) in mixtures of water and methanol. Two systems are studied: micellar solutions of polystyrene-b-poly(N-isopropylacrylamide) (PS-b-PNIPAM) diblock copolymers and, as a reference, solutions of PNIPAM homopolymers, both at a concentration of 20 mg/mL in DO. Using a stopped-flow instrument, fully deuterated methanol was rapidly added to these solutions at volume fractions between 10 and 20%. Time-resolved turbidimetry revealed aggregate formation within 10-100 s. The structural changes on mesoscopic length scales were followed by time-resolved small-angle neutron scattering (TR-SANS) with a time resolution of 0.1 s. In both systems, the pathway of the aggregation depends on the content of deuterated methanol; however, it is fundamentally different for homopolymer and diblock copolymer solutions: In the former, very large aggregates (>150 nm) are formed within the dead time of the setup, gradient appears at their surface in the late stages. In contrast, the growth of the aggregates in the latter system features different regimes, and the final aggregate size is 50 nm, thus much smaller than for the homopolymer. For the diblock copolymer, the time dependence of the aggregate radius can be described by two models: In the initial stage, the diffusion-limited coalescence model describes the data well; however, the resulting coalescence time is unreasonably high. In the late stage, a logarithmic coalescence model based on an energy barrier which is proportional to the aggregate radius is successfully applied. and a concentration Y1 - 2014 U6 - https://doi.org/10.1021/ma501434e SN - 0024-9297 SN - 1520-5835 VL - 47 IS - 19 SP - 6867 EP - 6879 PB - American Chemical Society CY - Washington ER - TY - JOUR A1 - Park, H. A1 - Walta, S. A1 - Rosencrantz, Ruben R. A1 - Koerner, A. A1 - Schulte, Christoph A1 - Elling, L. A1 - Richtering, Walter A1 - Böker, Alexander T1 - Micelles from self-assembled double-hydrophilic PHEMA-glycopolymer-diblock copolymers as multivalent scaffolds for lectin binding JF - Polymer Chemistry N2 - We introduce a novel double-hydrophilic hydroxyethylmethacrylate (HEMA) based diblock glycopolymer which self-assembles into homogeneous spherical micellar structures in water. The micellar structure renders surface-oriented N-acetylglucocosamine (GlcNAc) sugar moieties for strong multivalent glycan-mediated lectin binding. Structural analysis and lectin binding is performed by microscopy methods, dynamic light scattering (DLS) and two-focus fluorescence correlation spectroscopy (2fFCS), revealing a novel micellar type of multivalent sugar binding scaffold with high potential for biomedical applications. Y1 - 2016 U6 - https://doi.org/10.1039/c5py00797f SN - 1759-9954 SN - 1759-9962 VL - 7 SP - 878 EP - 886 PB - Royal Society of Chemistry CY - Cambridge ER -