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Polymers in Aqueous Lubrication
KTH, Skolan för kemivetenskap (CHE). KTH. (Surface and corrosion science)ORCID-id: 0000-0002-0191-9786
2017 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

The main objective of this thesis work was to gain understanding of the layer properties and polymer structures that were able to aid lubrication in aqueous media. To this end, three types of polyelectrolytes: a diblock copolymer, a train-of-brushes and two brush-with-anchor mucins have been utilized. Their lubrication ability in the boundary lubrication regime has been examined by Atomic Force Microscopy with colloidal probe.

The interfacial behavior of the thermoresponsive diblock copolymer, PIPOZ60-b-PAMPTAM17,on silica was studied in the temperature interval 25-50 ˚C. The main finding is that adsorption hysteresis, due to the presence of trapped states, is important when the adsorbed layers are in contact with a dilute polymer solution. The importance of trapped states was also demonstrated in the measured friction forces, where significantly lower friction forces, at a given temperature, were encountered on cooling than on the preceding heating stage, which was attributed to increased adsorbed amount. On the heating stage the friction force decreased with increasing temperature despite the worsening of the solvent condition, and the opposite trend was observed when using pre-adsorbed layers (constant adsorbed amount) as a consequence of increased segment-segment attraction.

The second part of the studies was devoted to the interfacial properties of mucins on PMMA. The strong affinity provided by the anchoring group of C-PSLex and C-P55 together with their more extended layer structure contribute to the superior lubrication of PMMA compared to BSM up to pressures of 8-9 MPa. This is a result of minor bridging and lateral motion of molecules along the surface during shearing. We further studied the influence of glycosylation on interfacial properties of mucin by utilizing the highly purified mucins, C-P55 and C-PSLex. Our data suggest that the longer and more branched carbohydrate side chains on C-PSLex provide lower interpenetration and better hydration lubrication at low loads compared to the shorter carbohydrate chains on C-P55. However, the longer carbohydrates appear to counteract disentanglement less efficiently, giving rise to a higher friction force at high loads.

sted, utgiver, år, opplag, sider
Stockholm: KTH Royal Institute of Technology, 2017. , s. 66
Serie
TRITA-CHE-Report, ISSN 1654-1081 ; 2017:15
Emneord [en]
Lubrication, boundary lubrication, friction, surface forces, adsorption, adsorption hysteresis, non-equilibrium state, diblock copolymer, polyelectrolyte, thermoresponsive, mucin, QCM-D, ellipsometry, AFM
HSV kategori
Forskningsprogram
Kemi
Identifikatorer
URN: urn:nbn:se:kth:diva-204931ISBN: 978-91-7729-305-7 (tryckt)OAI: oai:DiVA.org:kth-204931DiVA, id: diva2:1086946
Disputas
2017-03-31, Kollegiesalen, Brinellvägen 8, KTH-campus, Stockholm, 10:00 (engelsk)
Opponent
Veileder
Merknad

QC 20170407

Tilgjengelig fra: 2017-04-07 Laget: 2017-04-04 Sist oppdatert: 2017-04-07bibliografisk kontrollert
Delarbeid
1. Temperature-Dependent Adsorption and Adsorption Hysteresis of a Thermoresponsive Diblock Copolymer
Åpne denne publikasjonen i ny fane eller vindu >>Temperature-Dependent Adsorption and Adsorption Hysteresis of a Thermoresponsive Diblock Copolymer
Vise andre…
2014 (engelsk)Inngår i: Langmuir, ISSN 0743-7463, E-ISSN 1520-5827, Vol. 30, nr 15, s. 4333-4341Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

A nonionic-cationic diblock copolymer, poly(2-isopropyl-2-oxazoline)(60)-b-poly((3-acrylamidopropyl)- trimethylammonium chloride)(17), (PIPOZ(60)-b-PAMPTMA(17)), was utilized to electrostatically tether temperature-responsive PIPOZ chains to silica surfaces by physisorption. The effects of polymer concentration, pH, and temperature on adsorption were investigated using quartz crystal microbalance with dissipation monitoring and ellipsometry. The combination of these two techniques allows thorough characterization of the adsorbed layer in terms of surface excess, thickness, and water content. The high affinity of the cationic PAMPTMA(17) block to the negatively charged silica surface gives rise to a high affinity adsorption isotherm, leading to (nearly) irreversible adsorption with respect to dilution. An increase in solution pH lowers the affinity of PIPOZ to silica but enhances the adsorption of the cationic block due to increasing silica surface charge density, which leads to higher adsorption of the cationic diblock copolymer. Higher surface excess is also achieved at higher temperatures due to the worsening of the solvent quality of water for the PIPOZ block. Interestingly, a large hysteresis in adsorbed mass and other layer properties was observed when the temperature was cycled from 25 to 45 degrees C and then back to 25 degrees C. Possible causes for this temperature hysteresis are discussed.

Emneord
Irreversible adsorption, Negatively charged, Polymer concentrations, Quartz crystal microbalance with dissipation monitoring, Temperature hysteresis, Temperature-dependent adsorption, Temperature-responsive, Thermo-responsive
HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-145826 (URN)10.1021/la500377w (DOI)000334991400017 ()2-s2.0-84899408073 (Scopus ID)
Forskningsfinansiär
Swedish Research CouncilVinnova
Merknad

QC 20140604

Tilgjengelig fra: 2014-06-04 Laget: 2014-06-02 Sist oppdatert: 2017-12-05bibliografisk kontrollert
2. Tethered Poly(2-isopropyl-2-oxazoline) Chains: Temperature Effects on Layer Structure and Interactions Probed by AFM Experiments and Modeling
Åpne denne publikasjonen i ny fane eller vindu >>Tethered Poly(2-isopropyl-2-oxazoline) Chains: Temperature Effects on Layer Structure and Interactions Probed by AFM Experiments and Modeling
Vise andre…
2015 (engelsk)Inngår i: Langmuir, ISSN 0743-7463, E-ISSN 1520-5827, Vol. 31, nr 10, s. 3039-3048Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Thermoresponsive polymer layers on silica surfaces have been obtained by utilizing electrostatically driven adsorption of a cationic-nonionic diblock copolymer. The cationic block provides strong anchoring to the surface for the nonionic block of poly(2-isopropyl-2-oxazoline), referred to as PIPOZ. The PIPOZ chain interacts favorably with water at low temperatures, but above 46 degrees C aqueous solutions of PIPOZ phase separate as water becomes a poor solvent for the polymer. We explore how a change in solvent condition affects interactions between such adsorbed layers and report temperature effects on both normal forces and friction forces. To gain further insight, we utilize self-consistent lattice mean-field theory to follow how changes in temperature affect the polymer segment density distributions and to calculate surface force curves. We find that with worsening of the solvent condition an attraction develops between the adsorbed PIPOZ layers, and this observation is in good agreement with predictions of the mean-field theory. The modeling also demonstrates that the segment density profile and the degree of chain interpenetration under a given load between two PIPOZ-coated surfaces rise significantly with increasing temperature.

HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-165219 (URN)10.1021/la504653w (DOI)000351327300013 ()25686020 (PubMedID)2-s2.0-84925004133 (Scopus ID)
Merknad

QC 20150506

Tilgjengelig fra: 2015-05-06 Laget: 2015-04-24 Sist oppdatert: 2017-12-04bibliografisk kontrollert
3. Effect of solvent quality and chain density on normal and frictional forces between electrostatically anchored thermoresponsive diblock copolymer layers
Åpne denne publikasjonen i ny fane eller vindu >>Effect of solvent quality and chain density on normal and frictional forces between electrostatically anchored thermoresponsive diblock copolymer layers
Vise andre…
2017 (engelsk)Inngår i: Journal of Colloid and Interface Science, ISSN 0021-9797, E-ISSN 1095-7103, Vol. 487, s. 88-96Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Equilibration in adsorbing polymer systems can be very slow, leading to different physical properties at a given condition depending on the pathway that was used to reach this state. Here we explore this phenomenon using a diblock copolymer consisting of a cationic anchor block and a thermoresponsive block of poly(2-isopropyl-2-oxazoline), PIPOZ. We find that at a given temperature different polymer chain densities at the silica surface are achieved depending on the previous temperature history. We explore how this affects surface and friction forces between such layers using the atomic force microscope colloidal probe technique. The surface forces are purely repulsive at temperatures <40 degrees C. A local force minimum at short separation develops at 40 degrees C and a strong attraction due to capillary condensation of a polymer-rich phase is observed close to the bulk phase separation temperature. The friction forces decrease in the cooling stage due to rehydration of the PIPOZ chain. A consequence of the adsorption hysteresis is that the friction forces measured at 25 degrees C are significantly lower after exposure to a temperature of 40 degrees C than prior to heating, which is due to higher polymer chain density on the surface after heating.

sted, utgiver, år, opplag, sider
Academic Press, 2017
Emneord
Surface forces, Friction, Boundary lubrication, PIPOZ, Poly(2-isopropyl-2-oxazoline), Thermoresponsive polymer, Adsorption hysteresis
HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-198864 (URN)10.1016/j.jcis.2016.10.021 (DOI)000388550600011 ()27756003 (PubMedID)2-s2.0-84992378692 (Scopus ID)
Forskningsfinansiär
Swedish Research Council
Merknad

QC 20170103

Tilgjengelig fra: 2017-01-03 Laget: 2016-12-22 Sist oppdatert: 2017-11-29bibliografisk kontrollert
4. Comparison of a Brush-with-Anchor and a Train-of-Brushes Mucin on Poly(methyl methacrylate) Surfaces: Adsorption, Surface Forces, and Friction
Åpne denne publikasjonen i ny fane eller vindu >>Comparison of a Brush-with-Anchor and a Train-of-Brushes Mucin on Poly(methyl methacrylate) Surfaces: Adsorption, Surface Forces, and Friction
Vise andre…
2014 (engelsk)Inngår i: Biomacromolecules, ISSN 1525-7797, E-ISSN 1526-4602, Vol. 15, nr 4, s. 1515-1525Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Interfacial properties of two types of mucins have been investigated at the aqueous solution/poly(methyl methacrylate) (PMMA) interface. One is commercially available bovine submaxillary mucin, BSM, which consists of alternating glycosylated and nonglycosylated regions. The other one is a recombinant mucin-type fusion protein, PSGL-1/mIgG(2b), consisting of a glycosylated mucin part fused to the Fc part of an immunoglobulin. PSGL-1/mIgG(2b) is mainly expressed as a (timer upon production. A quartz crystal microbalance with dissipation was used to study the adsorption of the mucins to PMMA surfaces. The mass of the adsorbed mucin layers, including the adsorbed mucin and water trapped in the layer, was found to be significantly higher for PSGL-1/mIgG(2b) than for BSM. Atomic force microscopy with colloidal probe was employed to study interactions and frictional forces between mucin-coated PMMA surfaces. Purely repulsive forces of steric origin were Observed between PSGL-1/mIgG(2b) mucin layers, whereas a small adhesion was detected between BSM layers and attributed to bridging. Both mucin layers reduced the friction force between PMMA surfaces in aqueous solution. The reduction was, however, significantly more pronounced for PSGL-1/mIgG(2b). The effective friction coefficient between PSGL-1/mIgG(2b)-coated PMMA surfaces is as low as 0.02 at low loads, increasing to 0.24 at the highest load explored, 50 nN. In contrast, a friction coefficient of around 0.7 was obtained between BSM-coated PMMA surfaces. The large differences in interfacial properties for the two mucins are discussed in relation to their structural differences.

Emneord
Quartz-Crystal Microbalance, Giant Papillary Conjunctivitis, Hydrophobic Surfaces, Contact-Lenses, Shear Forces, Qcm-D, Viscoelastic Properties, Microscope Cantilevers, Ocular Surface, Mica Surfaces
HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-145592 (URN)10.1021/bm500173s (DOI)000334571600046 ()2-s2.0-84898657216 (Scopus ID)
Forskningsfinansiär
Swedish Research CouncilVinnova
Merknad

QC 20140611

Tilgjengelig fra: 2014-06-11 Laget: 2014-05-23 Sist oppdatert: 2017-12-05bibliografisk kontrollert
5. Influence of Glycosylation on Interfacial Properties of Recombinant Mucins: Adsorption, Surface Forces and Friction
Åpne denne publikasjonen i ny fane eller vindu >>Influence of Glycosylation on Interfacial Properties of Recombinant Mucins: Adsorption, Surface Forces and Friction
Vise andre…
(engelsk)Manuskript (preprint) (Annet vitenskapelig)
Abstract [en]

Interfacial properties of two brush-with-anchor mucins, C-P55 and C-PSLex, have been investigated at the aqueous solution/poly(methylmethacrylate) (PMMA) interface. Both are recombinant mucin-type fusion proteins, produced by fusing the glycosylated mucin part of P-selectin glycoprotein ligand-1 (PSLG-1) to the Fc part of a mouse immunoglobulin in two different cells. They are mainly expressed as dimers upon production. Analysis of the O-glycans shows that the C-PSLex mucin has the longer and more branched side chains, but C-P55 has slightly higher sialic acid content. The adsorption of the mucins to PMMA surfaces was studied by quartz crystal microbalance with dissipation. The sensed mass, including the adsorbed mucin and water trapped in the layer, was found to be similar for these two mucin layers. Atomic force microscopy with colloidal probe was employed to study surface and friction forces between mucin-coated PMMA surfaces. Purely repulsive forces of steric origin were observed between mucin layers on compression, whereas a small adhesion was detected between both mucin layers on decompression. This was attributed to chain entanglement. The friction force between C-PSLex-coated PMMA is lower than that between C-P55-coated PMMA at low loads, but vice versa at high loads. We discuss our results in terms of the differences in the glycosylation composition of these two mucins.

Emneord
mucin, glycosylation, brush-with-anchor, adsorption, surface forces, lubrication
HSV kategori
Forskningsprogram
Kemi
Identifikatorer
urn:nbn:se:kth:diva-204933 (URN)
Forskningsfinansiär
Swedish Research Council
Merknad

QC 20170418

Tilgjengelig fra: 2017-04-04 Laget: 2017-04-04 Sist oppdatert: 2017-04-18bibliografisk kontrollert

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