A novel ferric-phosphate induced shape memory (SM) hydrogel is prepared by the one-step copolymerization of isopropenyl phosphonic acid (IPPA) and acrylamide (AM) in the presence of a crosslinker polyethylene glycol diacrylate (PEGDA). Different from the traditional SM hydrogels, our SM hydrogel can be processed into various shapes as needed and recovers to its original form in ‘multiconditions’ such as in the presence of a reducing agent or in the presence of a competitive complexing agent. This unique feature is attributed to the fact that the oxidized ferric ions show a high complexation ability with phosphate groups of IPPA, which acts as a physical crosslinker to form the secondary networks within the hydrogels to induce the shape memory effect. The memory behavior was totally reversible, owing to Fe3+ that can be reduced to Fe2+ and extracted by the complexing agent. Particularly, the SM hydrogels exhibit controllable and good mechanical characteristics by introduction of the ferric ions, i.e., the elastic modulus can increase from 2 kPa to 70 kPa dramatically. Learning from biological systems, phosphate-metal ion based hydrogels could become an attractive candidate for various biomedical and environmental applications.

Shape memory hydrogels offer the ability to recover their permanent shape from temporarily trapped shapes without application of external forces. Here, we report a novel dual-responsive shape memory hydrogel with characteristic thermoplasticity. The water-insoluble hydrogel is prepared by simple ternary copolymerization of acrylamide (AM) and acrylic acid (AA) with low amounts of a cationic surfmer, in the absence of organic crosslinkers. Through either ionic/complex binding of carboxyl groups via trivalent cations or salt-dependent hydrophobic association, the hydrogel can memorize a temporary shape successfully, which recovers its permanent form in the presence of a reducing agent or deionized water. Besides, the unique thermoplasticity of the hydrophobic polyampholyte hydrogel allows the change of its permanent shape upon heating and the fixation after cooling, which is in strong contrast to the conventional chemically cross-linked shape memory hydrogels. This fascinating feature undoubtedly enriches the shape memory hydrogel systems. Thus, we believe that the facile strategy could provide new opportunities with regard to the design and practical application of stimulus-responsive hydrogel systems.

A novel thermally sensitive shape memory (SM) hydrogel is prepared by block copoly-merization of a cationic surfactant monomer, dimethylhexadecyl[2-(dimethylamino)ethylmethacrylate]ammoniumbromide (C(16)DMAEMA), and acrylamide (AM) in the presence of α-cyclodextrin (α-CD) using N,N'-methylenebisacrylamide (MBA) as a crosslinker. XRD, solid state (13)C NMR, and DSC measurements show that the crystalline domains, induced by the hydrogen bonds between α-CDs threaded on the hydrophobic units of the polymer chains through the host-guest approach, can reversibly melt and crystallize at different temperatures. Rheological measurements show that both the elastic modulus G' and viscous modulus G'' drastically change due to the formation and dissolution of the crystalline domains. These thermo-sensitive crystalline domains serve as reversible physical crosslinks, endowing the hydrogel with excellent SM properties. Cyclic experiments show that the hydrogel can recover to almost 100% of the deformation in each cycle and can be reused several times.

The Yellow River basin is a typical semi-arid river basin in northern China. Serious water shortages have negative impacts on regional socioeconomic development. Recent years have witnessed changes in streamflow processes due to increasing human activities, such as agricultural activities and construction of dams and water reservoirs, and climatic changes, e.g. precipitation and temperature. This study attempts to investigate factors potentially driving changes in different streamflow components defined by different quantiles. The data used were daily provides a theoretical framework for the study of the hydrological effects of human activities and climatic changes on basins over the globe.

No abstract

In this study, chitosan was successfully grafted onto the top surface of a bromomethylated poly(phenylene oxide) (BPPO) ultrafiltration membrane without pretreating the membrane at harsh conditions and/or using other cross-linkers. Due to the grafting of polar groups of chitosan onto the membrane top surface, the hydrophilicity of the membrane top surface and the polar component of the total surface energy are improved compared to the pristine BPPO membrane. Theoretical calculation shows that the polar component of surface energy is a major contributor to the reduction in interfacial free energy of the membrane surface and the interaction strength between foulants and membrane surface. Therefore, the foulants adsorbed onto the top surface of chitosan/BPPO composite membranes are much easier to desorb during the cleaning process and as a result, a higher flux recovery was obtained compared to the pristine BPPO membrane. Moreover, due to the antibacterial nature of chitosan, such composite membranes show a better antibacterial property and the antibacterial rate was improved by 70% in comparison with the pristine BPPO membrane.

A new C 22 tailed sarcosinate anionic surfactant, 2-(N-erucacyl-N-methyl amido) acetate (EMAA), has been synthesized by use of the erucic acid and a hydrotrope-sarcosine. In contrast to the common method, which blends the hydrotrope with a surfactant, the sarcosine has been introduced into the anionic surfactant through chemical modification. Interestingly, the resultant C 22 tailed anionic surfactant shows excellent water solubility despite the ultra-long alkyl chain. Besides, the EMAA also exhibits high surface activity, and pH controllable micelles to vesicles transition (MVT). Rheology studies have revealed that the rheological properties of EMAA solutions are influenced by the concentration, temperature, salt, and pH dramatically. Aside from the excellent water solubility, the original feature highlighted in this work is that such a new C 22 tailed sarcosinate anionic surfactant exhibits good temperature resistance.Compared to the potassium oleate (KOA), the zero-shear viscosity of the EMAA solution is nearly 3 orders of magnitude higher under the same conditions.

Semiconductor photocatalysis is an effective strategy for solving the problems of increasing energy demand and environmental pollution. ZnIn2S4-based semiconductor photocatalyst materials have attracted much attention in the field of photocatalysis due to their suitable energy band structure, stable chemical properties, and good visible light responsiveness. In this study, ZnIn2S4 catalysts were modified by metal ion doping, the construction of heterojunctions, and co-catalyst loading to successfully prepare composite photocatalysts. The Co-ZnIn2S4 catalyst synthesized by Co doping and ultrasonic exfoliation exhibited a broader absorption band edge. Next, an a-TiO2/Co-ZnIn2S4 composite photocatalyst was successfully prepared by coating partly amorphous TiO2 on the surface of Co-ZnIn2S4, and the effect of varying the TiO2 loading time on photocatalytic performance was investigated. Finally, MoP was loaded as a co-catalyst to increase the hydrogen production efficiency and reaction activity of the catalyst. The absorption edge of MoP/a-TiO2/Co-ZnIn2S4 was widened from 480 nm to about 518 nm, and the specific surface area increased from 41.29 m2/g to 53.25 m2/g. The hydrogen production performance of this composite catalyst was investigated using a simulated light photocatalytic hydrogen production test system, and the rate of hydrogen production by MoP/a-TiO2/Co-ZnIn2S4 was found to be 2.96 mmol·h−1·g−1, which was three times that of the pure ZnIn2S4 (0.98 mmol·h−1·g−1). After use in three cycles, the hydrogen production only decreased by 5%, indicating that it has good cycle stability.