Investigation of the collapse of bubbles after the impact of a piston on a liquid free surface

A novel technique based on the impact of a piston on a liquid confined in a vessel is described. Pressure measurements reveal that strong pressure variations (up to 100 atmospheres) with a rich content of frequencies are efficiently transmitted to the liquid. High‐speed camera visualizations show that pre‐existing millimetric bubbles always collapse during the first instants of the impact whereas the behavior of submillimetric bubbles depends on the features of the pressure evolution in the system. In addition to the impact velocity, the amount of gas/vapor trapped between the piston and the liquid's surface plays an important role on how pressure evolves. Only when negative pressure occurs tiny bubbles grow significantly and collapse. The violent collapse of bubbles promote turbulence and mixing at very small length‐scales which renders this technique interesting to intensify processes limited by heat and mass diffusion. © 2017 American Institute of Chemical Engineers AIChE J, 63: 2483–2495, 2017     

A DMA study of the interfacial changes on injection‐molded iPP/mica composites modified by a p‐phenylen‐bis‐maleamic acid grafted atactic polypropylene

Present work concerns to the study of the dynamic mechanical and thermal responses of selected polypropylene (iPP)/mica composites with a modified interface from the matrix side by using a p‐phenylen‐bis‐maleamic acid grafted atactic polypropylene, coming from a byproduct of industrial polymerization reactors. Thus, the study is mainly focused on the 75/25 iPP/mica ratio since it was identified in previous works as providing the maximum inter mica particle distance to assure they should participate in the overall process of dissipation of the mechanical energy supplied to the composites. Hence, the present dynamic mechanical analysis discussion tries to correlate the damping responses of the injection‐molded composites with those previously obtained but over compression molded composites as the basis of further studies all along the compositional iPP/mica map. Therefore, the latter let us, on the one hand, to follow how the main values of the different dynamic mechanical analysis parameters vary because of the interfacial modifier presence, and on the other, to develop a robust correlation between them and the corresponding macroscopic mechanical parameters. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45366.     

Influence of ionic liquid composition on the stability of polyvinyl chloride‐based ionic liquid inclusion membranes in aqueous solution

Membrane technology has gained significant importance with the incorporation of ionic liquids into their structure. This work shows the influence of ionic liquid composition on the stability of PVC‐based polymer ionic liquid inclusion membranes (PILIMs) in aqueous solution. Among the ILs investigated, those membranes which contain between 20 and 30%_w/w of the least soluble, [OMIM⁺][PF₆^?] and [OMIM⁺][Ntf₂^?], exhibit losses of IL lower than 10%. For both ILs, the amount immobilized was maximum for the membranes with 30%_w/w of IL (0.0838 and 0.0832 g, respectively). On the contrary, the ionic liquid loss increases as its solubility in water increase, reaching 99.52% when PILIMs are prepared with 70%_w/w of [OMIM⁺][BF₄^?]. The results demonstrate that the stability of PILIMs depends on the solubility of the IL in the surrounding phase and the specific interaction between the IL and the polymeric support for PVC‐to‐IL ratios higher than 30%_w/w. © 2016 American Institute of Chemical Engineers AIChE J, 63: 770–780, 2017     

Cover Image,Volume 66, Issue 10

The cover image, by Bruna A. Bregadiolli et al., is based on the Research Article Towards the synthesis of poly(azafulleroid)s: main chain fullerene oligomers for organic photovoltaic devices, DOI: 10.1002/pi.5419 .

     

Kirigami/Origami‐Based Soft Deployable Reflector for Optical Beam Steering

The beam steering mechanism has been a key element for various applications ranging from sensing and imaging to solar tracking systems. However, conventional beam steering systems are bulky and complex and present significant challenges for scaling up. This work introduces the use of soft deployable reflectors combining a soft deployable structure with simple kirigami/origami reflective films. This structure can be used as a macroscale beam steering mechanism that is both simple and compact. This work first develops a soft deployable structure that is easily scalable by patterning of soft linear actuators. This soft deployable structure is capable of increasing its height several folds by expanding in a continuous and controllable manner, which can be used as a frame to deform the linearly stretchable kirigami/origami structures integrated into the structure. Experiments on the reflective capability of the reflectors are conducted and show a good fit to the modeling results. The proposed principles for deployment and for beam steering can be used to realize novel active beam steering devices, highlighting the use of soft robotic principles to produce scalable morphing structures.     

<Emphasis Type="Italic">St-MMA-BuA</Emphasis> terpolymerization in emulsion: II. The kinetic azeotropy and the problem of homogeneity in composition

An analysis of the kinetic azeotropy of the terpolymer from styrene(St)-methyl methacrylate(MMA)-butyl acrylate(BuA) in emulsion polymerization is effectuated. The objective is to determine the conditions for obtaining terpolymers uniform in composition. In this regard, a composition near to the unitary azeotrope is used in batch, semicontinuous and seeded emulsion polymerization processes. As expected, the monomer partition between the different phases modifies the terpolymer composition, in particular at the beginning of the semicontinuous processes. It is also observed that the unitary azeotrope in batch and semicontinuous emulsion polymerization is conserved in a large range of conversion due to the constancy of monomer concentration and radicals in the particle. In this way, a terpolymer with almost an accumulated constant composition is obtained in the seeded process. A thermodynamic analysis of the kinetic azeotropy is also made. The correspondence between the azeotropes of the binary copolymers and the values of the Flory interaction parameters of the monomers χ _ιj is correlated. It is found that the lesser repulsion of the St-MMA pair respect to that of St-BuA provoked that the composition of the terpolymer tends to the copolymer azeotrope of St-MMA.     

Poly(ε-caprolactone) Diols (HOPCLOH) and Their Poly(ester-urethanes) (PEUs): The Effect of Linear Aliphatic Diols [HO–(CH2)m–OH] as Initiators

α,ω-Hydroxy telechelic poly(ε-caprolactones) were prepared by ring-opening polymerization of the ε-caprolactone catalyzed by ammonium decamolybdate in the presence of different aliphatic diols [HO–(CH₂)_m–OH, where m?=?2, 4, 6, 8, 10, 12, 14, and 16] as initiators to obtain a family of α,ω-hydroxy telechelic poly(ε-caprolactone) [HO–PCL–O–(CH₂)_m–O–PCL–OH, m?=?2, 4, 6, 8, 10, 12, 14, and 16]. The content of the alkyl group (AG) (–(CH₂)_m–) had an important effect on the crystallinity (x_i) of α,ω-hydroxy telechelic poly(ε-caprolactone), showing a proportional relationship. In poly(ester-urethanes) derived from α,ω-hydroxy telechelic poly(ε-caprolactones) and 1,6-hexamethylene diisocyanate, the AG also showed a similar effect on the x_i and eventually on the mechanical properties, increasing the values of the modulus. Therefore, AG content was a factor to induce a plastic behavior in poly(ester-urethanes). The effect of AG on the water uptake of poly(ester-urethanes) after 1 week was negligible.