Seelinger David, Biesalski Markus
Ernst-Berl-Institut Macromolecular and Paper Chemistry, Technical University Darmstadt, Alarich-Weiss-Str. 8, 64287 Darmstadt, Germany.
Gels. 2023 Mar 9;9(3):206. doi: 10.3390/gels9030206.
With the overarching aim for the development of sustainable, nontoxic wet strength agents for paper, a novel polymer gel system based on oxidized hydroxypropyl cellulose (keto-HPC) cross-linked with polyamines was investigated in detail to gain a deeper insight into the wet strength mechanism. When applied to paper, this wet strength system significantly increases the relative wet strength by using only low amounts of polymer, and it is therefore comparable with established wet strength agents based on fossil resources, such as polyamidoamine epichlorohydrin resins. With the help of ultrasonic treatment, keto-HPC was degraded with respect to its molecular weight and further cross-linked in paper using polymeric amine-reactive counterparts. The resulting polymer-cross-linked paper mechanical properties were analyzed with respect to the dry and wet tensile strength, respectively. In addition, we analyzed the polymer distribution using fluorescence confocal laser scanning microscopy (CLSM). If high-molecular-weight samples are being used for cross-linking, we do find accumulation of the polymer mainly on the surface of the fibers and at fiber crossing points, accompanied with enhancing strong effects on paper's wet tensile strength. In contrast, if low-molecular-weight (i.e., degraded) keto-HPC is being applied, the macromolecules are capable of entering the inner porous structure of the paper fibers, and almost no accumulation at the fiber crossing points is observed, which also results in a lowered wet paper tensile strength, respectively. This insight into wet strength mechanisms of the keto-HPC/polyamine system can thus lead to new opportunities for the development of alternative biobased wet strength agents where molecular weight dependence of the wet tensile properties allows for a fine tuning of mechanical properties in the wet state.
为了开发可持续、无毒的纸张湿强剂这一总体目标,对一种基于氧化羟丙基纤维素(酮化羟丙基纤维素,keto-HPC)与多胺交联的新型聚合物凝胶体系进行了详细研究,以更深入地了解湿强机理。当应用于纸张时,这种湿强体系仅使用少量聚合物就能显著提高相对湿强度,因此可与基于化石资源的成熟湿强剂(如聚酰胺多胺环氧氯丙烷树脂)相媲美。借助超声处理,酮化羟丙基纤维素的分子量降低,并使用聚合物胺反应性对应物在纸张中进一步交联。分别针对干拉伸强度和湿拉伸强度分析了所得聚合物交联纸张的机械性能。此外,我们使用荧光共聚焦激光扫描显微镜(CLSM)分析了聚合物分布。如果使用高分子量样品进行交联,我们确实发现聚合物主要积聚在纤维表面和纤维交叉点处,同时对纸张的湿拉伸强度有增强作用。相反,如果使用低分子量(即降解的)酮化羟丙基纤维素,大分子能够进入纸张纤维的内部多孔结构,并且几乎没有观察到在纤维交叉点处的积聚,这也分别导致湿纸拉伸强度降低。因此,对酮化羟丙基纤维素/多胺体系湿强机理的这种深入了解可为开发替代生物基湿强剂带来新机遇,其中湿拉伸性能对分子量的依赖性允许在湿态下对机械性能进行微调。