The present disclosure discloses a high-whiteness polyimide microfiber and a preparation method thereof and use. The polyimide fiber includes polyimide obtained from the reaction of wholly alicyclic dianhydride HTDA and an aromatic diamine monomer containing methyl or trifluoromethyl by chemical imidization. In the present disclosure, the polyimide microfiber has both excellent heat-resistant stability and spinning film-forming property, and the fabric has ultra-high whiteness. The microfiber fabric prepared from the polyimide fiber may be used as a component with high-temperature resistant and high-whiteness in personal protective equipment such as mask and protective clothing, and also may be used as an electronic component in the high-tech field such as aerospace, optoelectronic, microelectronic and automobile.

The present disclosure discloses a high-whiteness polyimide microfiber and a preparation method thereof and use. The polyimide fiber includes polyimide obtained from the reaction of wholly alicyclic dianhydride HTDA and an aromatic diamine monomer containing methyl or trifluoromethyl by chemical imidization. In the present disclosure, the polyimide microfiber has both excellent heat-resistant stability and spinning film-forming property, and the fabric has ultra-high whiteness. The microfiber fabric prepared from the polyimide fiber may be used as a component with high-temperature resistant and high-whiteness in personal protective equipment such as mask and protective clothing, and also may be used as an electronic component in the high-tech field such as aerospace, optoelectronic, microelectronic and automobile.

The present application provides methods for producing polybenzimidazole carbon fiber that does not require infusibilization treatment.

The present application provides methods for producing polybenzimidazole carbon fiber that does not require infusibilization treatment.

The present invention provides a porous carbon fiber which has an excellent permeation amount and excellent pressure resistance, which is prevented from the occurrence of detachment or cracking at an interface, and which can exhibit excellent properties needed for use as a support for a fluid separation membrane. The present invention is a porous carbon fiber having a bicontinuous porous structure, wherein the average value R.sub.ave of the R value of the outer surface and the R value of the inside is 1.0 or more and 1.8 or less, the absolute value ΔR of the difference between the R value of the outer surface and the R value of the inside is 0.05 or less, and R value is a carbonization progression degree calculated from a Raman spectrum in accordance with the following formula:
R value=(intensity of scattering spectrum at 1360 cm.sup.−1)/(intensity of scattering spectrum at 1600 cm.sup.−1).

A method comprising: providing at least one first composition comprising at least one conjugated polymer and at least one solvent, wet spinning the at least one first composition to form at least one first fiber material, hot-drawing the at least one fiber to form at least one second fiber material. In lead embodiments, high-performance poly(3,4-ethylenedioxy-thiophene)/poly(styrenesulfonate) (PEDOT/PSS) conjugated polymer microfibers were fabricated via wet-spinning followed by hot-drawing. In these lead embodiments, due to the combined effects of the vertical hot-drawing process and doping/de-doping the microfibers with ethylene glycol (EG), a record electrical conductivity of 2804 S.Math.cm.sup.−1 was achieved. This is believed to be a six-fold improvement over the best previously reported value for PEDOT/PSS fibers (467 S.Math.cm.sup.−1) and a twofold improvement over the best values for conductive polymer films treated by EG de-doping (1418 S.Math.cm.sup.−1). Moreover, these lead, highly conductive fibers experience a semiconductor-metal transition at 313 K. They also have superior mechanical properties with a Young's modulus up to 8.3 GPa, a tensile strength reaching 409.8 MPa and a large elongation before failure (21%). The most conductive fiber also demonstrates an extraordinary electrical performance during stretching/unstretching: the conductivity increased by 25% before the fiber rupture point with a maximum strain up to 21%. Simple fabrication of the semi-metallic, strong and stretchable wet-spun PEDOT/PSS microfibers can make them available for conductive smart electronics. A dramatic improvement in electrical conductivity is needed to make conductive polymer fibers viable candidates in applications such as flexible electrodes, conductive textiles, and fast-response sensors and actuators.

A method comprising: providing at least one first composition comprising at least one conjugated polymer and at least one solvent, wet spinning the at least one first composition to form at least one first fiber material, hot-drawing the at least one fiber to form at least one second fiber material. In lead embodiments, high-performance poly(3,4-ethylenedioxy-thiophene)/poly(styrenesulfonate) (PEDOT/PSS) conjugated polymer microfibers were fabricated via wet-spinning followed by hot-drawing. In these lead embodiments, due to the combined effects of the vertical hot-drawing process and doping/de-doping the microfibers with ethylene glycol (EG), a record electrical conductivity of 2804 S.Math.cm.sup.−1 was achieved. This is believed to be a six-fold improvement over the best previously reported value for PEDOT/PSS fibers (467 S.Math.cm.sup.−1) and a twofold improvement over the best values for conductive polymer films treated by EG de-doping (1418 S.Math.cm.sup.−1). Moreover, these lead, highly conductive fibers experience a semiconductor-metal transition at 313 K. They also have superior mechanical properties with a Young's modulus up to 8.3 GPa, a tensile strength reaching 409.8 MPa and a large elongation before failure (21%). The most conductive fiber also demonstrates an extraordinary electrical performance during stretching/unstretching: the conductivity increased by 25% before the fiber rupture point with a maximum strain up to 21%. Simple fabrication of the semi-metallic, strong and stretchable wet-spun PEDOT/PSS microfibers can make them available for conductive smart electronics. A dramatic improvement in electrical conductivity is needed to make conductive polymer fibers viable candidates in applications such as flexible electrodes, conductive textiles, and fast-response sensors and actuators.

The present invention relates to composites comprising rigid-rod polymers and graphene nanoparticles, processes for the preparation thereof, nanocomposite films and fibers comprising such composites and articles containing such nanocomposite films and fibers.

The present invention relates to composites comprising rigid-rod polymers and graphene nanoparticles, processes for the preparation thereof, nanocomposite films and fibers comprising such composites and articles containing such nanocomposite films and fibers.

Described herein are polyphenylene fibers. The polyphenylene fibers have one or more polyphenylene polymers. The polyphenylene fibers can further include one or more poly(aryl ether sulfone) polymers. In some embodiments, the polyphenylene fibers can have an average diameter that is less than about 1 micron. The polyphenylene fibers can have desirable mechanical properties. Also described herein are methods for forming polyphenylene fibers. In some embodiments, the fibers can be fabricated using specifically engineered polymer solutions in conjunctions with adapted force spinning techniques.