Effect of sodium dodecyl benzene sulfonate to the displacement performance of hyperbranched polymer

Experimental studies were conducted to realize displacement performance effect of anionic surfactant sodium dodecyl benzene sulfonate (SDBS) on hyperbranched poly(AM/AA/AMPS/GA), which was successfully synthesized via free radical polymerization using modified dendritic functional monomer (GA), acrylamide (AM), acrylate (AA), and 2-acrylamido-2-methyl propane sulfonic acid (AMPS). Compared with individual polymer, SP (surfactant polymer) binary systems showed lower apparent viscosity, interfacial tension, and hydrodynamic radius as the result of the electrostatic repulsion between the tail end of hydrophilic polymer branched chain and the head of the surfactant. It was found from abundant static adsorption and dynamic retention tests that the values of static adsorption and dynamics retention of SDBS which is mixed with hyperbranched polymer decrease due to the competitive interaction. However, unlike this phenomenon, SDBS would heighten the dynamic retention value of poly(AM/AA/AMPS/GA), resulting in addition of residual resistance factor. Oil displacement experiment indicated that SP solutions have greater capability of enhance oil recovery than individual polymer under same conditions.     

Preparation and properties of hyperbranched polymer containing functionalized Nano-SiO<Subscript>2</Subscript> for low-moderate permeability reservoirs

A novel water-soluble hyperbranched polymer (AA/AM/SMNS) consisting of functionalized Nano-SiO₂ as the core was synthesized by free-radical polymerization for low-moderate permeability reservoirs. The AA/AM/SMNS was carefully characterized by spectroscopic and electronic technologies. It was found that the microscopic structures of AA/AM/SMNS was denser and more regular in comparison to the linear polymer HPAM. The hydrodynamic radius of AA/AM/SMNS was 197 nm, less than the HPAM radius of 244 nm with similar molecular weight, so that the AA/AM/SMNS had a good matching relationship with pore throat in midpermeability reservoirs (100–500 mD). Besides, the introduction of Nano-SiO₂ endowed the AA/AM/SMNS remarkable thermal stability, shear resistance and viscoelasticity. Based on core flooding experiments, the AA/AM/SMNS could build high resistance factor and residual resistance factor in the corresponding porous medium. Furthermore, the sheared AA/AM/SMNS solution of 1500 mg L–1 performed excellent oil recovery of 15.47% in the 300 mD porous medium, which suggested the hyperbranched polymer based on modified Nano-SiO₂ have a valuable prospect for enhancing oil recovery in low-moderate permeability reservoirs.     

Synthesis and rheological property of various modified nano-SiO2/AM/AA hyperbranched polymers for oil displacement

Russian Journal of Applied Chemistry - In this study, various modified nano-SiO2 functional monomers (nano-SiO2-KH540-MAH) were prepared and reacted with acrylamide (AM) and acrylate (AA) to...     

西藜芦生物硷~1H核磁共振谱的研究

本文研究了西藜芦生物硷的1~H核磁共振谱,归纳出一些确定酰基连接位置的初步规律。     

Eco-friendly chitosan@silver/plant fiber membranes for masks with thermal comfortability and self-sterilization

The surgical masks have been essential consumables for public in the COVID-19 pandemic. However, long-time wearing masks will make wearers feel uncomfortable and massive discarded non-biodegradable masks lead to a heavy burden on our environment. In this paper, we adopt degradable chitosan@silver (CS@Ag) core–shell fibers and plant fibers to prepare an eco-friendly mask with excellent thermal comfort, self-sterilization, and antiviral effects. The thermal network of CS@Ag core–shell fibers highly improves the in-plane thermal conductivity of masks, which is 4.45 times higher than that of commercial masks. Because of the electrical conductivity of Ag, the fabricated mask can be electrically heated to warm the wearer in a cold environment and disinfect COVID-19 facilely at room temperature. Meanwhile, the in-situ reduced silver nanoparticles (AgNPs) endow the mask with superior antibacterial properties. Therefore, this mask shows a great potential to address the urgent need for a thermally comfortable, antibacterial, antiviral, and eco-friendly mask.

Graphical abstract

     

Polymer Photocatalysts Containing Segregated π-Conjugation Units with Electron-Trap Activity for Efficient Natural-light-driven Bacterial Inactivation

Development of highly efficient and metal-free photocatalysts for bacterial inactivation under natural light is a major challenge in photocatalytic antibiosis. Herein, we developed an acidizing solvent-thermal approach for inserting a non-conjugated ethylenediamine segment into the conjugated planes of 3,4,9,10-perylene tetracarboxylic anhydride to generate a photocatalyst containing segregated π-conjugation units (EDA-PTCDA). Under natural light, EDA-PTCDA achieved 99.9 % inactivation of Escherichia coli and Staphylococcus aureus (60 and 45 min), which is the highest efficiency among all the natural light antibacterial reports. The difference in the surface potential and excited charge density corroborated the possibility of a built-in electron-trap effect of the non-conjugated segments of EDA-PTCDA, thus forming a highly active EDA-PTDA/bacteria interface. In addition, EDA-PTCDA exhibited negligible toxicity and damage to normal tissue cells. This catalyst provides a new opportunity for photocatalytic antibiosis under natural light conditions.