Well-defined side-chain liquid-crystalline polysiloxanes

A route to well-defined side-chain liquid-crystalline polysiloxanes (ratio of weight-to number-average molar masses Mw/Mn < 1.2 is reported. Anionic ring-opening polymerization of pentamethylvinylcyclotrisiloxane yielded a poly(dimethylsiloxane-co-methylvinylsiloxane) backbone. A flexible disiloxane spacer was used to connect 4-(ω-alkenyloxy)-4'-cyanobiphenyl mesogenic molecules to the vinyl groups which belong to the backbone, leading to a side-chain liquid-crystalline polysiloxane (SCLCP) which has its mesogens distributed regularly along the main chain. Preliminary measurements indicate an electro-optic switching time s = 1 min at 20°C and 7 s at 32°C (dc, 5 V/µm))

Performance of Transition Metals in Imidazolium-Assisted CO₂ Reduction in Acetonitrile

This study explores the electrochemical reduction of CO2 in dry acetonitrile containing 1,3-dimethyl imidazolium cations, utilizing late-transition metals (Au, Ag, Zn, Cu, and Ni). All metals exhibit remarkable selectivity, nearing 100 %, for CO formation. Particularly noteworthy is Au, which manifests the lowest (−2.37 V vs. Ag/Ag+) overpotential in chronopotentiometry experiments. We propose that, for metals with lower CO binding energies compared to Au (Ag and Zn electrodes) – calculated by DFT, the rate-determining step is the adsorption of CO2. This distinction in CO2 adsorption is reinforced by the examination of partial charge transfer from negatively charged slabs to CO2 (−0.241 a.u with the Au electrode and +0.002 a.u with the Zn electrode). Conversely, the greater CO binding energy calculated for Cu and Ni likely diminishes electrocatalytic activity relative to the Au electrode. Our results unveil a volcano trend in catalyst activity, albeit with smaller performance disparities between the late-transition metals and Au than previously observed in aqueous conditions, possibly due to the co-catalytic influence of imidazolium cations. This study suggests that metals unsuitable for aqueous environments hold promise for cost-effective and viable electrochemical conversion of CO2 to CO in non-aqueous media containing imidazolium compounds.</p

Pattern transfer fidelity in capillary force lithography with poly(ferrocenylsilane) plasma etch resists

The influence of processing conditions and polymer architecture on pattern transfer in capillary force lithography (CFL) using poly(ferrocenylsilane) etch resists is investigated. Zero-shear-rate viscosities measured at different temperatures and for polymers with different molar masses are related to the quality of CFL patterns, assessed based on atomic force microscopy experiments. An optimal range of viscosities corresponding to appropriate molar masses and processing temperatures is established. In this range, polymers possess enough mobility allowing for reasonably quick surface pattern formation. Yet, the polymers are not too mobile and preserve their shape when quenched to below Tg prior to serving as etch resist masks

Smart Windows: Switching Light Transmittance by Responsive Organometallic Poly(ionic liquid)s: Control by Cross Talk of Thermal and Redox Stimuli (Adv. Funct. Mater. 41/2017)

In article number 1702784, G. Julius Vancso and co-workers report an organometallic polymer with sulfonate side groups for transmittance control. The novel polymer, produced by a simple one-step synthesis, exhibits both a lower critical solution temperature (LCST)-type phase transition and an “isothermal” redox-triggered phase transition in aqueous solution, leading to a new type of “smart window” by using thermal and electrical triggers

Polyester Brush Coatings for Circularity:Grafting, Degradation, and Repeated Growth

Polymer brushes are widely used as versatile surface modifications. However, most of them are designed to be long-lasting by using nonbiodegradable materials. This generates additional plastic waste and hinders the reusability of substrates. To address this, we present a synthetic strategy for grafting degradable polymer brushes via organocatalytic surface-initiated ring-opening polymerization (SI-ROP) from stable PGMA-based macroinitiators. This yields polyester brush coatings (up to 50 nm in thickness) that hydrolyze with controlled patterns and can be regrown on the same substrate after degradation. We chose polyesters of different hydrolytic stability and degradation mechanism, i.e., poly(lactic acid) (PLA), polycaprolactone (PCL), and polyhydroxybutyrate (PHB), which are grown from poly(glycidyl methacrylate) (PGMA)-based macroinitiators for strong surface binding and initiating site reuse. Brush degradation is monitored via thickness changes in pH-varied buffer solutions and seawater with PHB brushes showing rapid degradation in all solutions. PLA and PCL brushes show higher stability in solutions of up to pH 8, while all coatings fully degrade after 14 days in seawater. These brushes offer surface modifications with well-defined degradation patterns that can be regrown after degradation, making them an interesting alternative to (meth)acrylate-based, nondegradable polymers brushes.</p

Nonaqueous Interfacial Polymerization-Derived Polyphosphazene Films for Sieving or Blocking Hydrogen Gas

A series of cyclomatrix polyphosphazene films have been prepared by nonaqueous interfacial polymerization (IP) of small aromatic hydroxyl compounds in a potassium hydroxide dimethylsulfoxide solution and hexachlorocyclotriphosphazene in cyclohexane on top of ceramic supports. Via the amount of dissolved potassium hydroxide, the extent of deprotonation of the aromatic hydroxyl compounds can be changed, in turn affecting the molecular structure and permselective properties of the thin polymer networks ranging from hydrogen/oxygen barriers to membranes with persisting hydrogen permselectivities at high temperatures. Barrier films are obtained with a high potassium hydroxide concentration, revealing permeabilities as low as 9.4 × 10-17 cm3 cm cm-2 s-1 Pa-1 for hydrogen and 1.1 × 10-16 cm3 cm cm-2 s-1 Pa-1 for oxygen. For films obtained with a lower concentration of potassium hydroxide, single gas permeation experiments reveal a molecular sieving behavior, with a hydrogen permeance of around 10-8 mol m-2 s-1 Pa-1 and permselectivities of H2/N2 (52.8), H2/CH4 (100), and H2/CO2 (10.1) at 200 °C.</p

Well-defined side-chain liquid-crystalline polysiloxanes

A route to well-defined side-chain liquid-crystalline polysiloxanes (ratio of weight-to number-average molar masses Mw/Mn &lt; 1.2 is reported. Anionic ring-opening polymerization of pentamethylvinylcyclotrisiloxane yielded a poly(dimethylsiloxane-co-methylvinylsiloxane) backbone. A flexible disiloxane spacer was used to connect 4-(ω-alkenyloxy)-4'-cyanobiphenyl mesogenic molecules to the vinyl groups which belong to the backbone, leading to a side-chain liquid-crystalline polysiloxane (SCLCP) which has its mesogens distributed regularly along the main chain. Preliminary measurements indicate an electro-optic switching time s = 1 min at 20°C and 7 s at 32°C (dc, 5 V/µm))

Dual functionality of ferrocene-based metallopolymers as radical scavengers and nanoparticle stabilizing agents

The beneficial redox properties of ferrocene-based polymers have been utilized during in situ preparation of metallic nanoparticles, while such redox features also indicate great promise in applications as free radical..

Advances in Membrane Separation for Biomaterial Dewatering

Biomaterials often contain large quantities of water (50-98%), and with the current transition to a more biobased economy, drying these materials will become increasingly important. Contrary to the standard, thermodynamically inefficient chemical and thermal drying methods, dewatering by membrane separation will provide a sustainable and efficient alternative. However, biomaterials can easily foul membrane surfaces, which is detrimental to the performance of current membrane separations. Improving the antifouling properties of such membranes is a key challenge. Other recent research has been dedicated to enhancing the permeate flux and selectivity. In this review, we present a comprehensive overview of the design requirements for and recent advances in dewatering of biomaterials using membranes. These recent developments offer a viable solution to the challenges of fouling and suboptimal performances. We focus on two emerging development strategies, which are the use of electric-field-assisted dewatering and surface functionalizations, in particular with hydrogels. Our overview concludes with a critical mention of the remaining challenges and possible research directions within these subfields.</p

Collapse from the top: Brushes of poly(N-isopropylacrylamide) in co-nonsolvent mixtures

Using a combination of ellipsometry and friction force microscopy, we study the reversible swelling, collapse and variation in friction properties of covalently bound poly(N-isopropylacrylamide) (PNIPAM) layers on silicon with different grafting densities in response to exposure to good solvents and cononsolvent mixtures. Changes in the thickness and segment density distribution of grafted films are investigated by in situ ellipsometry. Based on quantitative modelling of the ellipsometry spectra, we postulate a structural model, which assumes that collapse takes place in the contacting layer between the brush and the co-nonsolvent and the top-collapsed brushes remain hydrated in the film interior. Using the structural model derived from ellipsometry spectra, we analyse the AFM based friction force microscopy data, which were obtained by silica colloidal probes. Results show a large increase of the friction coefficient of PNIPAM grafts when the grafts swollen by water are brought in contact with cononsolvents. For instance, the value of the friction coefficient for a medium density brush in water is four times lower than the value observed in a water–methanol (50% v/v) mixture. This increase of friction is accompanied by an increase in adherence between the PNIPAM chains and the silica colloidal probes, and is a result of chain collapse in the graft when contacted by a co-nonsolvent mixture in agreement with the model postulated on the basis of ellipsometric characterisation. The kinetic behaviour of the collapse is assessed by measuring the temporal variation of friction in situ as a function of elapsed time following contact with the co-nonsolvent as a function of graft density. In conclusion, the effect of cononsolvency influenced both the thickness of the PNIPAM brushes and the tribological behavior of the brush surfaces