Preparation and Characterisation of Polyurethane Acrylate-Based Titanium Dioxide Pigment for Blue Light-Curable Ink

Herein, a polyurethane acrylate-based TiO2 (PU-TiO2) was fabricated using a two-step method. First, a polyurethane prepolymer was prepared. Second, PU-TiO2 was prepared using amino-modified TiO2 (A-TiO2). The best synthesis process of the polyurethane prepolymer was when the reaction temperature was 80 °C, the reaction time was 3 h and the R-value of the polyurethane acrylate was 2. Next, the influence of the A-TiO2 content on the structure and performance of PU-TiO2 was examined. The analysis of the rheological properties of the PU-TiO2 ink indicated that its viscosity gradually increased as the A-TiO2 content increased. The tensile performance of film improved because of the presence of A-TiO2. The photo-polymerisation and photo-rheological performance indicated that the PU-TiO2 structure changed from a hyperbranched structure with TiO2 as the core to a segmented structure, as the A-TiO2 content was 3%.

Interaction of polyamidoamine dendrimers and amphiphylic dendrons with lipid membranes

Polyamidoamine (PAMAM) dendrimers and amphiphilic dendrons are one of the types of nanomaterials characterized by a hyperbranched structure of polymer branches. In the case of dendrimers, the dendrons are covalently linked at the central focal point. In the case of amphiphilic dendrons, dendrons are non-covalently linked by hydrophobic interactions, forming micellar structures. These nanoparticles are widely used in biology and medicine as contrast agents, carriers of drugs and genetic material. Their use in scientific practice requires an understanding of the basic mechanisms of their interaction with membranes – the main obstacle to the entry of dendrimers into the cell. This review discusses the regularities of the interaction of dendrimers and amphiphilic dendrons with lipid membranes. Various models of dendrimer-membrane interactions are described as the basis for the penetration of dendrimers and amphiphilic nanoparticles into cells. Keywords: polyamidoamine dendrimers, amphiphilic dendrons, lipid membranes, cells, antitumor therapeutics, antibacterial agents, diagnostics, genetic therapy.

High toughness and excellent electrical performance bismaleimide resin modified by hyperbranched unsaturated polyester of flexible aliphatic side chains

Because of its flawed toughness, the scope of application of bismaleimide resin (BMI) in the field of aeronautics, industry and electricity is greatly restricted. Herein, a novel Hyperbranched unsaturated polymers (HBP) with the flexible chains grafted was incorporated to reinforce BMI resin’s toughness, where the new interpenetrating networks (IPN) structure was formed. The rich unsaturated double bond of HBP polyester could react with the BMI resin for chemical crosslinking and be used for the toughening agent. 13C-NMR and FT-IR were used to characterize HBP’s hyperbranched structure. Consequently, after adding 20 wt.% HBP, the impact strength of BMI modified by HBP increased by 211.1%. In comparison with neat BMI, the flexural strength of BMI modified by HBP was enhanced by 209.3%. It is worth noticing that HBP available in BMI resin significantly improved its electrical performance.

Synthesis of Multicyclic Polymer with Hyperbranched Structure by Click Polymerization of AB2 Cyclic Macromonomer

Multicyclic polymer with hyperbranched structure was successfully synthesized. A tailored initiator containing a protected alkynyl group was prepared and used to initiate atom transfer radical polymerization (ATRP) of styrene. By...

A novel route to improve the mechanical and rheological properties of HTPE/AP/Al propellant by adding a modified hyperbranched polyester

Both better mechanical and rheological properties are pursued for composite solid propellant. In this work, varying proportions of a modified hyperbranched polyester (MHBPE) were added to HTPE/AP/Al propellant. The static tensile property as one kind of mechanical properties of MHBPE/HTPE/AP/Al propellant were found to be superior to those of blank HTPE/AP/Al propellant as a result of the entanglement and interpenetration of molecular chains caused by the introduction of the hyperbranched structure. Evaluations on the related improved creep resistance and stress relaxation performance further demonstrated the advantages of introduction of MHBPE to HTPE/AP/Al propellant. Rheological properties of HTPE/AP/Al propellant with and without MHBPE during the casting process were investigated and compared and the results confirmed the improvement benefiting from low viscosity and loose void structure. Thus, modified hyperbranched polyester provided a novel route to potentially meet the requirements for propellant manufacturing and applications.

Enhanced Hydroxide Conductivity and Dimensional Stability with Blended Membranes Containing Hyperbranched PAES/Linear PPO as Anion Exchange Membranes

A series of novel blended anion exchange membranes (AEMs) were prepared with hyperbranched brominated poly(arylene ether sulfone) (Br-HB-PAES) and linear chloromethylated poly(phenylene oxide) (CM-PPO). The as-prepared blended membranes were fabricated with different weight ratios of Br-HB-PAES to CM-PPO, and the quaternization reaction for introducing the ionic functional group was performed by triethylamine. The Q-PAES/PPO-XY (quaternized-PAES/PPO-XY) blended membranes promoted the ion channel formation as the strong hydrogen bonds interconnecting the two polymers were maintained, and showed an improved hydroxide conductivity with excellent thermal behavior. In particular, the Q-PAES/PPO-55 membrane showed a very high hydroxide ion conductivity (90.9 mS cm−1) compared to the pristine Q-HB-PAES membrane (32.8 mS cm−1), a result supported by the morphology of the membrane as determined by the AFM analysis. In addition, the rigid hyperbranched structure showed a suppressed swelling ratio of 17.9–24.9% despite an excessive water uptake of 33.2–50.3% at 90 °C, and demonstrated a remarkable alkaline stability under 2.0 M KOH conditions over 1000 h.

Room-temperature autonomous self-healing glassy polymers with hyperbranched structure

Glassy polymers are extremely difficult to self-heal below their glass transition temperature (Tg) due to the frozen molecules. Here, we fabricate a series of randomly hyperbranched polymers (RHP) with high density of multiple hydrogen bonds, which showTgup to 49 °C and storage modulus up to 2.7 GPa. We reveal that the hyperbranched structure not only allows the external branch units and terminals of the molecules to have a high degree of mobility in the glassy state, but also leads to the coexistence of “free” and associated complementary moieties of hydrogen bonds. The free complementary moieties can exchange with the associated hydrogen bonds, enabling network reconfiguration in the glassy polymer. As a result, the RHP shows amazing instantaneous self-healing with recovered tensile strength up to 5.5 MPa within 1 min, and the self-healing efficiency increases with contacting time at room temperature without the intervention of external stimuli.