Tang Qianqian, Yang Rong, Li Jinnuo, Zhou Mingsong, Yang Dongjie
Henan Key Laboratory of Function-Oriented Porous Materials, College of Chemistry and Chemical Engineering, Luoyang Normal University, 6 Jiqing Road, Yibin District, Luoyang 471934, China.
State Key Laboratory of Pulp and Paper Engineering, School of Chemistry and Chemical Engineering, South China University of Technology, 381 Wushan Road, Tianhe District, Guangzhou 510640, China.
Molecules. 2024 Aug 21;29(16):3940. doi: 10.3390/molecules29163940.
In this paper, N-vinylpyrrolidone was copolymerized with acrylic acid and itaconic acid by free radical polymerization, and a series of polyacrylic acid-co-itaconic acid-co-N-vinylpyrrolidone (PAIN) dispersants with different pyrrolidone ligand contents were synthesized and characterized. Then, the cobalt blue nano-pigment slurry (20 wt%) was prepared through a water-based grinding method, and the optimum grinding technology was explored and determined as follows: PAIN2 as a dispersant, a dispersant dosage of 10 wt%, and a grinding time of 480 min. According to this optimum grinding technology, the prepared pigment slurry had a significantly decreased agglomeration, the of which was 82 nm, and separately increased to 130 nm and 150 nm after heat storage for 3 and 7 days, exhibiting excellent heat storage stability. Additionally, its TSI value was also the lowest (1.9%), indicating good dispersion stability. The QCM and adorption capacity measuring results showed PAIN2 had a larger adsorption capacity, and the formed adsorption layer had a higher rigidity and was not easy to fall off. This was caused by both the interaction of carboxyl groups and the pyrrolidone ligand (strong coordination interaction) in PAIN2 with cobalt blue. The XPS and FT-IR measurements further proved the above-mentioned adsorption mechanism.
本文通过自由基聚合将N-乙烯基吡咯烷酮与丙烯酸和衣康酸共聚,合成并表征了一系列具有不同吡咯烷酮配体含量的聚丙烯酸-衣康酸-N-乙烯基吡咯烷酮(PAIN)分散剂。然后,通过水基研磨法制备了钴蓝纳米颜料浆料(20 wt%),并探索并确定了最佳研磨工艺如下:以PAIN2作为分散剂,分散剂用量为10 wt%,研磨时间为480 min。按照该最佳研磨工艺制备的颜料浆料团聚明显减少,其粒径为82 nm,在3天和7天蓄热后分别增大至130 nm和150 nm,表现出优异的蓄热稳定性。此外,其TSI值也最低(1.9%),表明具有良好的分散稳定性。QCM和吸附容量测量结果表明PAIN2具有较大的吸附容量,形成的吸附层具有较高的刚性且不易脱落。这是由于PAIN2中的羧基与吡咯烷酮配体(强配位相互作用)与钴蓝之间的相互作用所致。XPS和FT-IR测量进一步证实了上述吸附机理。