Chen, Yen ChuanYen ChuanChenHuang, Ying ChiYing ChiHuangHuang, Yi HuaYi HuaHuangLin, Ying FengYing FengLinHuang, Ho ChingHo ChingHuangRU-JONG JENGCheng, Yu WeiYu WeiChengWu, Chien HsinChien HsinWu2023-10-302023-10-302023-12-0122133437https://scholars.lib.ntu.edu.tw/handle/123456789/636663The development of raw materials from methane and carbon dioxide holds significant potential to cut greenhouse gas (GHG) emissions and reduce the global carbon footprint. As an important monomer, vinyl acetate (VAc) can be produced by the consumption of acetic acid, which will potentially contribute to the reduction of GHGs emission. However, polymers based on VAc are usually prepared from emulsion polymerization in water which brings about the challenges of using modification processes to improve their properties. Here, a newly developed crosslink was able to establish covalently adaptable networks directly in water, enabling the formation of a poly(vinyl acetate) (PVAc) composite. As a result, PVAc emulsions using a monomer of 100% VAc could be transformed from a soft and weak adhesive polymer into an elastomeric polymer composite network with an elongation (775%) at break and flexibility. With the enhanced rubbery modulus, the polymer possesses characteristics for shape-memory material applications with 93% shape fixity and 99% shape recovery after repeated deformation and shape fixity for three times. The recyclability of the PVAc thermosets was demonstrated after granulating and remolding three times, representing an opportunity for designing a greenhouse gas fixing material.CO fixation 2 | Covalent adaptable networks | Elastomer | Shape memory | Waterborne poly(vinyl acetate)[SDGs]SDG12[SDGs]SDG13journal article10.1016/j.jece.2023.1111702-s2.0-85173506191https://api.elsevier.com/content/abstract/scopus_id/85173506191