Polymers

Paiva, Diana;Pereira, André M.;Pires, Ana L.;Martins, Jorge;Carvalho, Luísa H.;Magalhães, Fernão D.

doi: 10.3390/polym10090985pmid: 30960910

Microparticles of corn starch and chitosan crosslinked with glutaraldehyde, produced by the solvent exchange technique, are studied as reinforcement fillers for thermoplastic corn starch plasticized with glycerol. The presence of 10% w/w chitosan in the microparticles is shown to be essential to guaranteeing effective crosslinking, as demonstrated by water solubility assays. Crosslinked chitosan forms an interpenetrating polymer network with starch chains, producing microparticles with a very low solubility. The thermal stability of the microparticles is in agreement with their polysaccharide composition. An XRD analysis showed that they have crystalline fraction of 32% with Va-type structure, and have no tendency to undergo retrogradation. The tensile strength, Young’s modulus, and toughness of thermoplastic starch increased by the incorporation of the crosslinked starch/chitosan microparticles by melt-mixing. Toughness increased 360% in relation to unfilled thermoplastic starch.

Qin, Yanlin;Lin, Xuliang;Lu, Yaoqin;Wu, Siyuan;Yang, Dongjie;Qiu, Xueqing;Fang, Yanxiong;Wang, Tiejun

doi: 10.3390/polym10090982pmid: 30960907

A novel grafting hydroxypropyl sulfonated and blocking condensed lignin (GSBAL) dye dispersant was prepared based on alkali lignin (AL) by sulfonation and etherification reactions. The significant increase in the sulfonic group content and the molecular weight endow GSBAL with excellent dispersity and stability at high temperatures. More importantly, the unfavorable property of the reducing effect of AL was largely reduced since over 80% of the phenolic hydroxyl groups were blocked. The functional azo groups in the dye could be mostly retained. The reducing rate of dye with GSBAL was decreased to 6.54% (25 °C), much lower than 18.62% for sulfomethylated alkali lignin (SAL) and 15.73% for sodium lignosulfonate (NaLS). The dispersity and exhaustion of the dye bath with GSBAL dispersant was significantly improved compared with that of a dye bath with SAL and NaLS.

Demirci, Serkan

doi: 10.3390/polym10090956pmid: 30960881

Crosslinked-polymer brushes give rise to new opportunities for functionalizing, protecting, and structuring both organic and inorganic materials. In this study, pH- and temperature-switchable crosslinked-polymer brushes were easily prepared by combining the in situ method with reversible addition–fragmentation chain transfer (RAFT) polymerization. Initially, the RAFT agent was immobilized on an amine-terminated silicon wafer surface and utilized in the surface-initiated RAFT polymerization of 2-N-morpholinoethyl methacrylate (MEMA) as a monomer, and β-cyclodextrin methacrylate (CDMA) was used as a crosslinker on the silicon substrate. Measurements of film thickness, water contact angle, surface morphology, and structural characteristics of the resulting surfaces confirmed the poly(2-N-morpholinoethyl methacrylate) (PMEMA) brush-gels. Reversible capture and release measurements of methylene blue as a model molecule were also performed by UV–vis analysis. The switchable properties of the PMEMA brush-gels were maintained over five cycles. The results indicate that these PMEMA brush-gels with reversible capture and release properties might have widespread potential applications, including improved diagnostic tools as well as bioseparation.

Niiyama, Eri;Uto, Koichiro;Lee, Chun Man;Sakura, Kazuma;Ebara, Mitsuhiro

doi: 10.3390/polym10091018pmid: 30960944

We have developed a smart anti-cancer fiber mesh that is able to control tumor-killing activity against lung adenocarcinoma precisely. The mesh is capable of carrying large loads of chemotherapeutic drug, paclitaxel (PTX), as well as magnetic nanoparticles (MNPs). The mesh generates heat when the loaded MNPs are activated in an alternating magnetic field (AMF). The mesh is thermo-responsive, so the heat generated can be also used to trigger PTX release from the mesh. An electrospinning method was employed to fabricate the mesh using a copolymer of N-isopropylacrylamide and N-hydroxymethylacrylamide, the phase transition temperature of which was adjusted to the mild-hyperthermia temperature range around 43 °C. In vitro anti-tumor studies demonstrated that both MNP- and PTX-loaded mesh killed about 66% of cells, whereas only PTX-loaded mesh killed about 43% of cells. In a mouse lung cancer model, the thermo-chemotherapy combo displayed enhanced anti-tumor activity and the systemic toxic effects on mice were eliminated due to local release of the chemotherapeutic agents. The proposed fiber system might provide a blueprint to guide the design of the next generation of local drug delivery systems for safe and effective cancer treatment.

Chen, Yanqin;Jiang, Chao;Cho, Chongdu

doi: 10.3390/polym10090971pmid: 30960896

In this paper, a commercial gas diffusion layer is used, to quantitatively study the correlation between its compressive characteristics and its operating temperature. In polymer electrode membrane fuel cells, the gas diffusion layer plays a vital role in the membrane electrode assembly, over a wide range of operating temperatures. Therefore, understanding the thermo-mechanical performance of gas diffusion layers is crucial to design fuel cells. In this research, a series of compressive tests were conducted on a commercial gas diffusion layer, at three different temperatures. Additionally, a microscopical investigation was carried out with the help of a scanning electron microscope, to study the evolution and development of the microstructural damages in the gas diffusion layers which is caused by the thermo-mechanical load. From the obtained results, it could be concluded that the compressive stiffness of the commercial gas diffusion layer depends, to a great extent, on its operational temperature.

Yan, Xiang;Cayla, Aurélie;Devaux, Eric;Salaün, Fabien

doi: 10.3390/polym10091031pmid: 30960956

Composites of polypropylene (PP) and water soluble poly(vinyl alcohol) (PVA) can become an environmentally friendly precursor in preparing porous material, and their biphasic morphology needs to be manipulated. In this work, PP-PVA extrudates were prepared with a twin-screw extruder, and different PP/PVA ratios were employed to manipulate the morphology of the blends. Afterwards, different silicas were imbedded within the blends to further regulate the biphasic microstructure. PVA continuity, as a vital parameter in obtaining porous material, was determined by selective extraction measurement, and PP-PVA biphasic morphology was characterized by scanning microscopy analyses (SEM). Rheological measurement was also performed to correlate the microstructure evolution of the blends. First, it was found that with the increment of PVA proportion, PVA continuity is raised gradually, and the microstructure of blends containing 40–50 wt % of PVA is approaching co-continuous. Second, the localization of silicas was predicted based on the wettability of silica and polymers, and it was also confirmed by TEM that different silicas showed selective distribution. It is inspiring that R972 nanoparticles were found mainly distributed at the interface, which gives a possibility in preparing a surface-modified porous material. The shape distribution and average size of PVA nodules were examined by analyzing the SEM images. It is indicated that silicas with different wettabilities play disparate roles in tuning the biphasic microstructures, leading to heterogeneous PVA continuity.

Vijayan, Veena;Uthaman, Saji;Park, In-Kyu

doi: 10.3390/polym10090983pmid: 30960908

Biomimetic functionalization of nanoparticles through camouflaging with cellular membranes has emerged as a promising strategy for cancer theragnostics. Cellular membranes used for camouflaging nanoparticles are generally isolated from blood cells, immune cells, cancer cells, and stem cells. The camouflaging strategy of wrapping nanoparticles with cellular membranes allows for superior tumor targeting through self-recognition, homotypic targeting and prolonged systematic circulation, thereby aiding in effective tumor therapy. In this review, we emphasized the various types of cellular membrane-camouflaged nanoparticles, their mechanisms in targeted therapy and various biomimetic strategies for anti-cancer therapy.

Yang, Teng-Chun

doi: 10.3390/polym10090976pmid: 30960901

Wood fiber-reinforced polylactic acid (PLA) composites (WFRPCs) were used as a filament to manufacture the unidirectional WFRPC components by means of fused deposition modeling (FDM). The physico-mechanical properties of the WFRPC components printed at different extrusion temperatures (200, 210, 220, and 230 °C) were determined. The results revealed that most of the physical properties (moisture content, surface roughness, water absorption rate, and thickness swelling rate) of the printed WFRPC component were not significantly influenced by extrusion temperature, while its density and color difference increased as the extrusion temperature increased. Additionally, the tensile and flexural properties of the FDM-printed WFRPC component decreased when the extrusion temperature was more than 200 °C, whereas the compressive strength and internal bond strength increased by 15.1% and 24.3%, respectively, when the extrusion temperature was increased from 200 to 230 °C. Furthermore, scanning electronic microscopy (SEM) demonstrated that the fracture surface of the tensile component printed at a higher extrusion temperature exhibited a better compatibility at fiber/PLA interfaces and good adhesion between the extruded filament segments. These results indicate that the FDM printing process using different extrusion temperatures has a substantial impact on the surface color, density, and mechanical properties of the printed WFRPC component.

Nonoguchi, Yoshiyuki;Sato, Dai;Kawai, Tsuyoshi

doi: 10.3390/polym10090962pmid: 30960887

The evaluation of thermoelectric properties has recently become a standard method for revealing the electronic properties of conducting polymers. Herein we report on the thermoelectric properties of a two-dimensional coordination polymer pellets. The pellets of Ni3(2,3,6,7,10,11-hexaiminotriphenylene)2, which has recently been developed, show n-type thermoelectric transport, dependent on crystallinity. The present results provide systematic feedback to the guideline for high-performance molecular thermoelectric materials.

Mehravar, Ehsan;Gross, Michael A.;Leal, Gracia Patricia;Reck, Bernd;Leiza, Jose R.;Asua, José M.

doi: 10.3390/polym10090975pmid: 30960900

A waterborne pressure-sensitive adhesive (PSA) that shows high adhesive performance and easy debondability on demand without leaving residues on the substrate (adhesive failure) has been developed. A key component of the PSA is a semicrystalline phase that is beneficial for the adhesive properties and that becomes fluid when heated above the melting temperature. Migration of this liquid-like polymer to the substrate-adhesive interface and hardening upon cooling results in a hard non-tacky interface that facilitates debonding. The effect of the particle morphology on the debonding ability is discussed.