Due to the characteristics of simple operation and low process cost, TYPE I Non-woven Sterile Disposable Medical Protective Coveralls have the ability of one-way wetting through finishing and other methods, which is an improved method widely used in actual production. The technicians used FG-910 fluorine-containing water-repellent finishing agent to finish the pure cotton spunlace non-woven fabric. It was found that when the concentration of the finishing solution was 40 g/L, the finished sample could achieve good unidirectional moisture conductivity, which could quickly The sweat produced by the wearer is exported, thereby ensuring the dryness and comfort of the wearer.

  The main raw material of TYPE I Non-woven Sterile Disposable Medical Protective Coveralls is polypropylene spunbond nonwoven. The cross-section of polypropylene filaments in polypropylene spunbond nonwovens is generally circular. The absence of grooves and pores makes it difficult for the moisture and sweat generated by the wearer to drain out of the body quickly. In actual production, by changing the shape of the spinneret hole of the spunbond non-woven equipment, the profiled fiber technology can be applied to improve the thermal and wet comfort of TYPE I Non-woven Sterile Disposable Medical Protective Coveralls.
  The polyethylene protective film commonly used in the existing medical protective clothing can effectively improve the barrier ability of the protective clothing, but the air permeability of the protective clothing after coating is poor, which reduces the wearer's experience. Therefore, the use of nano-protective film can take into account the protection, moisture permeability and breathability of the neckline and back of medical protective clothing, and can effectively improve the wearing comfort of TYPE I Non-woven Sterile Disposable Medical Protective Coveralls.
  Since TYPE I Non-woven Sterile Disposable Medical Protective Coveralls mainly adopts the design structure of sealed opening, it is difficult to achieve temperature regulation by air convection. Therefore, if phase change material or phase change microcapsules are used for post-processing on the neckline and back of medical protective clothing, the temperature regulation ability of medical protective clothing will be effectively increased, thereby improving the heat and humidity of TYPE I Non-woven Sterile Disposable Medical Protective Coveralls. comfort.
  The technical research on improving the heat and humidity comfort of TYPE I Non-woven Sterile Disposable Medical Protective Coveralls involves clothing engineering, physics, physiology and other disciplines. Although this type of research has a certain foundation, there is still room for further improvement and refinement in fiber raw materials, structural design, and post-processing methods. At present, the existing methods for improving the heat and humidity comfort of medical protective clothing have their own characteristics, but there are problems such as high price and environmental pollution. Therefore, finding cost-effective improvement methods to improve the thermal and wet comfort of TYPE I Non-woven Sterile Disposable Medical Protective Coveralls is still the focus of research. In addition, how to transform theoretical research into a simple and easy production process, whether medical protective clothing can ensure its good protective performance after improving its thermal and humid comfort, etc. These are all issues that need to be focused on in the research on improving the thermal and humid comfort of medical protective clothing.​​
  The above are some knowledge points about TYPE I Non-woven Sterile Disposable Medical Protective Coveralls. I hope you can study and understand the relevant knowledge carefully and choose the equipment that suits your needs.