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Reversible water driven chirality inversion in cellulose-based helices isolated from Erodium awns

Publication . Almeida, Ana; Querciagrossa, Lara; Silva, Pedro; Gonçalves, Filipa; Canejo, João; Almeida, Pedro L.; Godinho, Maria Helena; Zannoni, Claudio

Among the movements observed in some cellulosic structures produced by plants are those that involve the dispersion and burial of seeds, as for example in Erodium from the Geraniaceae plant family. Here we report on a simple and efficient strategy to isolate and tune cellulose-based hygroscopic responsive materials from Erodium awns’ dead tissues. The stimuli-responsive material isolated forms left-handed (L) or right-handed (R) helical birefringent transparent ribbons in the wet state that reversibly change to R helices when the material dries. The humidity-driven motion of dead tissues is most likely due to a composite material made of cellulose networks of fibrils imprinted by the plant at the nanoscale, which reinforces a soft wall polysaccharide matrix. The inversion of the handedness is explained using computational simulations considering filaments that contract and expand asymmetrically. The awns of Erodium are known to present hygroscopic movements, forming R helices in the dry state, but the possibility of actuating chirality via humidity suggests that these cellulose-based skeletons, which do not require complicated lithography and intricate deposition techniques, provide a diverse range of applications from intelligent textiles to micro-machines.

2019-04-07Journal article

Restricted access

The ultrafiltration performance of cellulose acetate asymmetric membranes: a new perspective on the correlation with the infrared spectra

Publication . Figueiredo, Ana Sofia; Garcia, Ana Rosa; Minhalma, Miguel; ILHARCO, LAURA; Pinho, Maria de

Integral asymmetric cellulose acetate (CA) membranes were casted by phase-inversion with formamide varying content - 22, 30 and 34% - as pore promoter. These membranes, CA-22, CA-30 and CA-34, were analyzed by infrared spectroscopy in attenuated total reflection mode (ATR-FTIR) to investigate the porous membrane matrix influence on the polymer/water/solute interactions and the selective ultrafiltration of salts. The membranes covered a wide range of hydraulic permeabilities, from 3.5 to 81.0 kg.m-2.h-1.bar-1, and of molecular weight cut-offs, from 4.17 to 31.43 kDa. The experimental apparent rejection coefficients of neutral solutes of increasing molecular weight are related to their intrinsic rejection coefficients through the film model. The surface average pore radius, estimated by an iterative algorithm, ranges from 2.1 to 4.5 nm. The tighter membrane, CA-22, displays experimental apparent rejection coefficients to the Na2SO4, CaSO4, MgSO4 of 50% or higher values and this is in contrast with the lower values, between 14 and 18%, to the NaCl, CaCl2 and MgCl2 salts. The ATR-FTIR evidences that in the membranes with larger pores, CA-30 and CA-34, the water molecules are organized with a liquid-water-like structure, in which most molecules are hydrogen bonded to four or to two others; nevertheless, a fraction of water molecules is strongly bonded to the CA carbonyl groups. For the CA-22 membrane, there are more free carbonyl groups and a larger fraction of free water, both able to interact with solutes, such as the hydrated sulphate ions. Therefore, this ultrafiltration membrane has the capability of differentiating anionic species.

2019-09-28Journal article

Open access