Markus Johannes Henricus Bulters

Bio: Markus Johannes Henricus Bulters is an academic researcher from DSM. The author has contributed to research in topics: Polymer & Coating. The author has an hindex of 11, co-authored 21 publications receiving 919 citations.

Toughening Elastomers with Sacrificial Bonds and Watching Them Break

Abstract: Elastomers are widely used because of their large-strain reversible deformability. Most unfilled elastomers suffer from a poor mechanical strength, which limits their use. Using sacrificial bonds, we show how brittle, unfilled elastomers can be strongly reinforced in stiffness and toughness (up to 4 megapascals and 9 kilojoules per square meter) by introducing a variable proportion of isotropically prestretched chains that can break and dissipate energy before the material fails. Chemoluminescent cross-linking molecules, which emit light as they break, map in real time where and when many of these internal bonds break ahead of a propagating crack. The simple methodology that we use to introduce sacrificial bonds, combined with the mapping of where bonds break, has the potential to stimulate the development of new classes of unfilled tough elastomers and better molecular models of the fracture of soft materials.

Coated optical fibers

Abstract: The invention relates to coated optical fibers comprising soft primary coatings and to such primary coatings for protecting glass optical fibers having a sufficient high resistance against cavitation. In particular, the primary coatings have a cavitation strength at which a tenth cavitation appears (σ 10 cav ) of at least about 1.0 MPa as measured at a deformation rate of 0.20% min −1 and of at least about 1.4 times their storage modulus at 23° C. The coating preferably shows strain hardening in a relative Mooney plot, preferably has a strain energy release rate Go of about 20 J/m 2 or more, and preferably has a low volumetric thermal expansion coefficient. The invention furthermore provides a method and apparatus for measuring the cavitation strength of a primary coating.

Numerical analysis of flow mark surface defects in injection molding flow

Abstract: In order to elucidate the mechanism of flow mark surface defects, the stability of injection molding flow is investigated numerically using a transient finite element method. Experiments performed by Schepens and Bulters [Bulters, M., and A. Schepens, “The origin of the surface defect ‘slip-stick’ on injection moulded products,” Paper IL-3-2, in Proceedings of the 16th Annual Meeting of the Polymer Processing Society, Shenghai, China, 2000a, pp. 144–145] using a novel two color injection molding technique are summarized and they indicate that surface defects are caused by a flow instability near the free surface during filling of the mold. Steady finite element calculations of a model injection molding flow using a single mode, exponential Phan-Thien–Tanner constitutive equation supply information about the base state streamlines and polymer stresses. By varying the parameters of the model, the degree of strain hardening in the extensional viscosity can be controlled. Then a linear stability analysis is u...

Fiber diameter control in electrospinning

Abstract: A simple model is proposed to predict the fiber diameter in electrospinning. We show that the terminal diameter is determined by the kinetics of the jet elongation—under the influence of the electric and viscous forces—and the solvent evaporation. Numerical and simple scaling analyses are performed, predicting the fiber diameter to scale as a power 1/3 of viscosity and 2/3 of polymer solution throughput divided by electrical current. Model predictions show a good agreement to our own electrospinning experiments on polyamide-6 solutions as well as to the data available in the literature.

Self-Healing Hydrogels

Abstract: Over the past few years, there has been a great deal of interest in the development of hydrogel materials with tunable structural, mechanical, and rheological properties, which exhibit rapid and autonomous self-healing and self-recovery for utilization in a broad range of applications, from soft robotics to tissue engineering. However, self-healing hydrogels generally either possess mechanically robust or rapid self-healing properties but not both. Hence, the development of a mechanically robust hydrogel material with autonomous self-healing on the time scale of seconds is yet to be fully realized. Here, the current advances in the development of autonomous self-healing hydrogels are reviewed. Specifically, methods to test self-healing efficiencies and recoveries, mechanisms of autonomous self-healing, and mechanically robust hydrogels are presented. The trends indicate that hydrogels that self-heal better also achieve self-healing faster, as compared to gels that only partially self-heal. Recommendations to guide future development of self-healing hydrogels are offered and the potential relevance of self-healing hydrogels to the exciting research areas of 3D/4D printing, soft robotics, and assisted health technologies is highlighted.

Tough and Water-Insensitive Self-Healing Elastomer for Robust Electronic Skin.

Abstract: An electronic (e-) skin is expected to experience significant wear and tear over time. Therefore, self-healing stretchable materials that are simultaneously soft and with high fracture energy, that is high tolerance of damage or small cracks without propagating, are essential requirements for the realization of robust e-skin. However, previously reported elastomers and especially self-healing polymers are mostly viscoelastic and lack high mechanical toughness. Here, a new class of polymeric material crosslinked through rationally designed multistrength hydrogen bonding interactions is reported. The resultant supramolecular network in polymer film realizes exceptional mechanical properties such as notch-insensitive high stretchability (1200%), high toughness of 12 000 J m-2 , and autonomous self-healing even in artificial sweat. The tough self-healing materials enable the wafer-scale fabrication of robust and stretchable self-healing e-skin devices, which will provide new directions for future soft robotics and skin prosthetics.

Fracture and adhesion of soft materials: a review.

Abstract: Soft materials are materials with a low shear modulus relative to their bulk modulus and where elastic restoring forces are mainly of entropic origin. A sparse population of strong bonds connects molecules together and prevents macroscopic flow. In this review we discuss the current state of the art on how these soft materials break and detach from solid surfaces. We focus on how stresses and strains are localized near the fracture plane and how elastic energy can flow from the bulk of the material to the crack tip. Adhesion of pressure-sensitive-adhesives, fracture of gels and rubbers are specifically addressed and the key concepts are pointed out. We define the important length scales in the problem and in particular the elasto-adhesive length Γ/E where Γ is the fracture energy and E is the elastic modulus, and how the ratio between sample size and Γ/E controls the fracture mechanisms. Theoretical concepts bridging solid mechanics and polymer physics are rationalized and illustrated by micromechanical experiments and mechanisms of fracture are described in detail. Open questions and emerging concepts are discussed at the end of the review.

Tough Stimuli-Responsive Supramolecular Hydrogels with Hydrogen-Bonding Network Junctions

Abstract: Hydrogels were prepared with physical cross-links comprising 2-ureido-4[1H]-pyrimidinone (UPy) hydrogen-bonding units within the backbone of segmented amphiphilic macromolecules having hydrophilic poly(ethylene glycol) (PEG). The bulk materials adopt nanoscopic physical cross-links composed of UPy–UPy dimers embedded in segregated hydrophobic domains dispersed within the PEG matrix as comfirmed by cryo-electron microscopy. The amphiphilic network was swollen with high weight fractions of water (wH2O ≈ 0.8) owing to the high PEG weight fraction within the pristine polymers (wPEG ≈ 0.9). Two different PEG chain lengths were investigated and illustrate the corresponding consequences of cross-link density on mechanical properties. The resulting hydrogels exhibited high strength and resilience upon deformation, consistent with a microphase separated network, in which the UPy–UPy interactions were adequately shielded within hydrophobic nanoscale pockets that maintain the network despite extensive water content....