Abstract: A high-strength creep-resistant polyester industrial yarn and preparation method thereof are provided. The high-strength creep-resistant polyester industrial yarn is prepared by spinning, winding and coordination treatment of a modified polyester after solid-state polycondensation to increase viscosity. The condition of coordination treatment is 60-72 hours at 80-100° C. The coordination agent is AgNO3, FeCl2, CuCl2, or NiCl2. The polyester segments of the prepared high-strength creep-resistant polyester industrial yarn includes a terephthalic acid segment, an ethylene glycol segment and a 2-(4-pyridine) terephthalic acid segment, and 2-(4-pyridine) terephthalic acid segments of different polyester segments are coordinated by metal ions (Ag+, Fe2+, Cu2+ or Ni2). The molar ratio of the terephthalic acid segment to the 2-(4-pyridine) terephthalic acid segment is 1:(0.03-0.05). The N atom on the pyridine of the 2-(4-pyridine) terephthalic acid segment is involved in coordination.

Abstract: A preparation method of fibers for medical antibacterial fabric includes cooling an antibacterial polyester melt by ring-blowing after extruded from a trilobal spinneret hole on a spinneret, and manufacturing a fully drawn yarn (FDY), then performing a relaxation heat treatment to obtain the fiber. The shapes and sizes of three leaves from different trilobal spinneret holes are the same; wherein all the trilobal spinneret holes are distributed in concentric circles, and the direction of the shortest leaf in each trilobal spinneret hole is randomly distributed. The prepared fiber has a three-dimensional crimp shape and includes antibacterial polyester monofilaments with trilobal cross-section. The fiber has mechanical performance indices as a crimp shrinkage of 26-29%, a crimp stability of 78-82%, a shrinkage elongation of 55-62%, a crimp elastic recovery rate of 70-75%, a breaking strength of 2.4-2.6 cN/dtex, an elongation at break of 55.0±5.0%, and a monofilament fineness of 1.00-1.50 dtex.