In the process of achieving carbon peak and carbon neutralization, it is very important to promote the electrification of rural energy consumption. Considering an acquaintance society context, this paper constructs a game model for the promotion of rural energy consumption electrification based on network game theory and analyzes the dynamic impact of different policies on the diffusion of rural households' energy consumption electrification behavior through numerical simulation. The results show that under the existing promotion model in China’s rural regions, the electrification level of rural energy use can be increased to 80% within approximately 20 years. In addition, the higher the government's cost sharing ratio, publicity efforts, and infrastructure construction level, the better the effectiveness of electrification promotion. It can increase the electrification ratio of rural energy consumption to 80% within 10 years when we set the government's cost sharing ratio and publicity efforts to 0.8, respectively. The environmental awareness, new technology mastery ability, and reputation loss from non-participation of farmers all have a significant positive impact on the effectiveness of electrification promotion. Notebly, when we increase the reputation loss of farmers to 1000, we can achieve complete electrification of rural energy use within 8 years. Finally, In addition, the direct cost and benefit of different energy consumption are different, and the promotion effect will be worse if the cost of rural households’ electrification transformation is higher. Improving electric power infrastructure, strengthening publicity and education, and building demonstration projects are the key measures to promote the electrification of rural energy consumption.

The current study is aimed at investigating the effect of cationic charge density and hydrophobicity on the antibacterial and hemolytic activities. Two kinds of cationic surfmers, containing single or double hydrophobic tails (octyl chains or benzyl groups), and the corresponding homopolymers were synthesized. The antimicrobial activity of these candidate antibacterials was studied by microbial growth inhibition assays against Escherichia coli, and hemolysis activity was carried out using human red blood cells. It was interestingly found that the homopolymers were much more effective in antibacterial property than their corresponding monomers. Furthermore, the geminized homopolymers had significantly higher antibacterial activity than that of their counterparts but with single amphiphilic side chains in each repeated unit. Geminized homopolymers, with high positive charge density and moderate hydrophobicity (such as benzyl groups), combine both advantages of efficient antibacterial property and prominently high selectivity. To further explain the antibacterial performance of the novel polymer series, the molecular interaction mechanism is proposed according to experimental data which shows that these specimens are likely to kill microbes by disrupting bacterial membranes, leading them unlikely to induce resistance.

A novel amphiphilic homopolymer (PAGC8), containing two hydrophilic head groups and double hydrophobic tails in each repeat unit, has been prepared by solution polymerization and named as "a geminized amphiphilic homopolymer" in this paper, which is capable of self-assembling into various nanoobjects depending on the solution concentration and solvent properties. Characterization of the self-assembly behaviors was carried out by steady-state fluorescence, transmission electron microscopy and nuclear magnetic resonance techniques. Particular emphasis was dedicated to the environmental responsiveness of the assemblies. The morphologies were observed to transform from micelle-type to vesicles on adding a certain amount of ethanol. It is noteworthy that the assemblies were able to trap hydrophilic (rhodamine B) and hydrophobic (Sudan Red) molecules. Subsequently different nanoobjects were found after the encapsulation. To probe the effect of the topological structure on the self-assembly behaviors, the properties of an additional homopolymer with single charge pendant architecture on the backbone were investigated for comparison. Significant differences in structure between the two architectures brought out remarkable variations in aggregates, which were non-responsive to the solvent environment, or encapsulation of molecules. Based on the experimental results, we proposed a possible mechanism of the morphological transitions of the assemblies.

A novel amphiphilic polyelectrolyte denoted as PAGC8 and a traditional amphiphilic polyelectrolyte denoted as PASC8 were prepared. PAGC8 consisted of gemini-type surfactant segment based on 1,3-bis (N,N-dimethyl-N-octylammonium)-2-propyl acrylate dibromide, while PASC8 incorporated acryloyloxyethyl-N,N-dimethyl-N-dodecylammonium bromide as single chain surfactant units within its repeat unit structure. Turbidity, stability, and zeta potential measurements were performed in the presence of PAGC8 and PASC8, respectively, to evaluate their effectiveness in inducing solid/liquid separations. It was found that the maximum transmittance was observed before the zeta potential values reached the isoelectric point, implying that not only charge neutralization but also charge-patch mechanism contributed to the separation process. Colloid probe atomic force microscopy technique was introduced to directly determine the interactions between surfaces in the presence of ultrahighly charged amphiphilic polyelectrolyte. On the basis of the AFM results, we have successfully interpreted the influence of the charge density of the polyelectrolytes on the phase stability. Electrostatic interaction played the dominant role in the flocculation processes, although both electrostatic interaction and hydrophobic effect provided contributions to the colloidal dispersions. The attractions upon surfaces approach in the case of PAGC8 were significantly larger than that of PASC8 due to the higher charge density. The strong peeling events upon retraction in the presence of PAGC8 implied that the hydrophobic effect was stronger than that of PASC8, which displayed the loose pulling events. A strong attraction was identified at shorter separation distances for both systems. However, these interactions cannot be successfully described by the Derjaguin-Landau-Verwey-Overbeek (DLVO) theory of colloid stability due to the participation of charge-patch and strong hydrophobic effect. To account for the additional interactions, we proposed an extended DLVO empirical model to explain the non-DLVO forces in the systems. A reasonable physical model was also proposed to further describe the interactions between surfaces in the two amphiphilic polyelectrolyte systems.