A filter medium including: a porous first support; nanofiber webs respectively stacked at the upper and lower parts of the first support, and made of a plurality of nanofibers of which the diameters have a standard deviation of 300 nm or less; and a porous second support interposed between the first support and the nanofiber web. The filter medium is implemented by fibers having uniform diameters, and thus is easily manufactured to have a predetermined pore diameter and simultaneously has excellent uniformity of the pore diameters, thereby having excellent filtering efficiency and being more suitable when selectively separating specific objects. Backwashing is enabled at uniform pressure during backwashing such that high cleaning power is obtained. The filter medium has excellent water permeability and excellent mechanical strength so as to minimize the shape and structural deformation and damage of the filter medium.

The invention relates to a highly aligned and closely packed electrospun fiber assembly, wherein the fibers have at least an extension part or pore on the surface thereof. The invention also relates to a microtube array membrane (MTAM), comprising fiber assembly of the present disclosure. The invention also relates to the applications of these electrospun fiber assemblies in biological applications, and method of manufacturing these electrospun fiber assemblies.

A nanostructured composite membrane filter for rapid water purification and methods for preparing the nanostructured composite membrane filter are provided. The nanostructured composite membrane includes a silver layer having a plurality of silver functionalized nanofibers for disinfecting microorganisms of water, and a chemical modified layer having a plurality of chemical modified nanofibers for removing impurities from the water. The plurality of silver functionalized nanofibers includes a plurality of polyvinyl alcohol (PVA) nanofibers coated with polydopamine (PDA) and silver, and each of the plurality of chemical modified nanofibers includes a polymer matrix such as polyvinyl alcohol (PVA) and anionic polyelectrolytes such as poly (sodium styrenesulfonate) (PSSNa) for capturing metal ions of the water.

Electrospun poly(acrylic) acid (PAA)/poly(vinyl) alcohol PVA nanofibers and integrated filtration membranes generated therefrom are disclosed herein. The membranes are suitable for use in selectively removing heavy metals such as lead and cadmium from water. The surface of the nanofibers is preferably functionalized with one or more chelating agents. The membranes have a high removal efficiency and adsorption capacity with well-distributed hid-density heavy metal adsorption sites with strong binding affinities for targeted heavy metals.

The disclosure discloses an anti-haze anti-harmful gas air filter membrane as well as a preparation method and application thereof. The air filter membrane comprises a nano fiber membrane made of nano fibers and having a two-dimensional or three-dimensional network structure. The nano fiber membrane can be a high-molecular polymer nano fiber membrane prepared by utilizing an electrostatic spinning process, and can also be doped with an organic or inorganic additive capable of adsorbing and absorbing harmful gases, such as VOCs, NO.sub.x, SO.sub.x and NH.sub.3, in the air and/or a photocatalyst capable of degrading these harmful gases in a photocatalysis manner, or the like. The anti-haze anti-harmful gas air filter membrane disclosed by the disclosure can efficiently filter PM2.5 and PM10 particulate pollutants and the like in the air and simultaneously can efficiently identify and clear multiple harmful gases in the air. The anti-haze anti-harmful gas air filter membrane has a wide application prospect in the field of air purification, for example, can be applied to air purification devices, such as screen windows, gauze masks and filter screens.

A multidimensional printer makes a multidimensional structure from a liquid composition and includes: an energetic crosslinking particle source; a vacuum chamber that receives energetic crosslinking particles from the energetic crosslinking particle source; a membrane that transmits the energetic crosslinking particles; and a sample chamber that: receives a liquid composition that includes a solvent and polymers, the polymers including a cross-linkable moiety subjected to the energetic crosslinking particles such that portions of the polymers proximate to the cross-linkable moieties subjected to the energetic crosslinking particles crosslink to form a solid crosslinked polymer structure, wherein the membrane isolates a vacuum of the vacuum chamber from vapor of the liquid composition in the sample chamber.

A filtration membrane comprising cellulose fibres, the membrane having a pore size distribution such that the modal pore diameter is between 10 nm and 25 nm and/or wherein less than 5% of the pore volume comprises pores of greater than 40 nm and having a total porosity greater than 30%.

A novel fibrous membrane comprises at least one substrate layer comprising at least 80% by weight of microfibers that carry positively charged and/or negatively charged functional groups, and at least one layer of filtration material attached to the substrate layer, wherein the layer of filtration material comprises at least 80% by weight of nanofibers that carry negatively charged and/or positively charged functional groups. The fibrous membrane is able to remove or reduce the concentration of bacteria, viruses and heavy metals while maintaining relatively high water flow. A filter comprising the fibrous membrane and a method for manufacturing the fibrous membrane are also provided.

Embodiments herein relate to medical devices and methods for monitoring and/or treatment including the use of synthetic polymers exhibiting specific binding for compounds such as disease state markers or toxic substances. In an embodiment, a method of testing a patient for a disease state is included, the method can include withdrawing a fluid sample from the patient and contacting the fluid sample with an extracorporeal monitoring device. The extracorporeal monitoring device can include a microporous membrane. The microporous membrane can include a synthetic polymer, wherein the synthetic polymer exhibits binding specificity with a disease state marker. The method can further include evaluating the extracorporeal monitoring device for the presence of the disease state marker. Other embodiments are included herein.

Disclosed herein are rolled-membrane microfluidic diffusion devices and corresponding methods of manufacture. Also disclosed herein are three-dimensionally printed microfluidic devices and corresponding methods of manufacture. Optionally, the disclosed microfluidic devices can function as artificial lung devices.