Juntao Wang,Shao-Lu Li,Yaxu Guan,Can Zhu,Genghao Gong,Yunxia Hu
Membrane fouling and degradation caused by free chlorine oxidation seriously hinder the long-term operation of aromatic polyamide (PA) thin-film-composite (TFC) membranes. In this study, sulfonamide monomers 4-aminobenzene sulfonamide (4-ABSA) and 2-aminoethanesulfonamide (2-AESA)) were facilely grafted onto the PA RO membranes surface via layer-by-layer interfacial polymerization (LbL-IP) method, endowing with much improved water flux, antifouling, and chlorine-resistance properties. The chemical compositions and surface properties of the RO membranes were systematically investigated by various techniques, as FTIR and XPS results clearly showed that sulfonamide groups were successfully grafted onto RO membranes’ surface. Compared to the pristine membrane, the water flux of the two modified membranes increased by 50.8% and 59.1%, reached 3.65 ± 0.15 L m −2 h −1 bar −1 and 3.85 ± 0.05 L m −2 h −1 bar −1 , respectively, meanwhile their NaCl rejection remained above 99.25 ± 0.08%. Due to the improvement of surface hydrophilicity and decrease of surface roughness , the antifouling performance of the modified membranes was greatly improved. Moreover, the N–H moieties on sulfonamide can act as sacrificial units for free chloride attack to significantly improve the chlorine-resistance performances of the modified RO membranes compared to the pristine one, with NaCl rejection remain above 98.95 ± 0.09% after chlorination intensity of 8000 ppm⋅h under acidic condition of pH 4. This simple and efficient surface grafting strategy and modifying materials make it have great application potential in the field of water treatment.
Zhaoqian Fan,Kun Gao,Linsong Wang,Yukun Qin,Song Liu,Ronge Xing,Huahua Yu,Kecheng Li,Pengcheng Li
Chitosan oligosaccharide (COS) modification is a feasible way to develop novel green nematicides. This study involved the synthesis of various COS sulfonamide derivatives via hydroxylated protection and deprotection, which were then characterized using NMR, FTIR, MS, elemental analysis, XRD, and TG/DTG. In vitro experiments found that COS-alkyl sulfonamide derivatives ( S6 and S11 – S13 ) exhibited high mortality (>98 % at 1 mg/mL) against Meloidogyne incognita second-instar larvaes (J2s) among the derivatives. S6 can cause vacuole-like structures in the middle and tail regions of the nematode body and effectively inhibit egg hatching. In vivo tests have found that S6 has well control effects and low plant toxicity. Additionally, the structure-activity studies revealed that S6 with a high degree of substitution, a low molecular weight, and a sulfonyl bond on the amino group of the COS backbone exhibited increased nematicidal activity. The sulfonamide group is a potential active group for developing COS-based nematicides.