Embodiments relate generally to a filter, for example, for attachment onto a gas detector device or a gas sensor, and attempt to improve the efficiency and service life of the filter. Embodiments typically comprise a dustproof membrane and a waterproof membrane. Some embodiments may also comprise a splash-proof cap and/or features to reduce negative pressure on the filters.

Disclosed are apparatus and methods for blood and other biological fluid purification using a membrane with cell containing vascular channel systems and filtration channel systems. Also disclosed are methods of making the apparatus as well as methods of making membranes.

The present invention relates to a crossflow membrane module configured to separate a feed fluid into a permeate fluid and a residue fluid across one or more membrane sheet(s). The crossflow module comprises a second end offset from a first end along the first direction where an inlet is provided at the first end and an outlet is provided at the second end. The one or more membrane sheet(s) each have a first portion and a second portion. A conduit is adjacent to the first side of each membrane sheet and is configured to receive and output the permeate fluid separated from the feed fluid. The second portion of the membrane sheet has a greater permeance for a major component than the first portion such that the second part of the permeate fluid, which is generated by separation across the second portion of the membrane sheet, has a higher concentration of the major component than the first part of the permeate fluid, which is generated by separation across the first portion. The second portion is spaced apart from the first side of the membrane sheet along the second direction thereby causing the second part of the permeate gas to flow towards the first side of the membrane sheet such that the second part of the permeate gas mixes with the first part of the permeate gas thereby reducing the concentration of the minor component in the first part of the permeate gas.

A device for enabling controlled movement of ions between a first ion-containing fluid and second ion-containing fluid comprises at least one cationic exchange membrane positioned between the first and second ion-containing fluids, and at least one anionic exchange membrane in parallel with the at least one cationic exchange membrane positioned between the first and second ion-containing fluids. The one or more of the at least one cationic exchange membrane and the at least one anionic exchange membrane is a membrane electrode assembly comprising an ion exchange membrane, and one or more permeable electrodes embedded within the ionic exchange membrane. The number of cationic exchange membranes and the number of anionic exchange membranes is the same, and the ions move through the membrane electrode assembly in response to a variable capacitive charge.

The present teaching relates to method, system, medium, and implementations for storage management. A hash table is constructed, having an index file having one or more slots, each of which includes one or more buckets. Each bucket stores one or more types of records, including a direct record, an indirect record, and a forwarding record. A direct record stores data directly in a bucket of a slot of the index file. When a storage request is received related to some relevant data, the request is handled based on the constructed hash table.

An oxygenator apparatus for use in an extracorporeal circuit. The apparatus includes a housing and a membrane assembly disposed within the housing. The membrane assembly includes a first plurality of gas exchange elements disposed in a first zone and a second plurality of gas exchange elements disposed in a second zone. The second zone is arranged concentrically around the first zone. The first and second plurality of gas exchange elements are fluidly open along a body and fluidly separated along a distal end. The first zone is configured to be fluidly coupled to an oxygen source and the second zone is configured to be fluidly coupled to a negative pressure source. A blood flow path includes a generally radial flow through the first zone to add oxygen to the blood and the second zone to separate gaseous micro emboli from the blood through the plurality of gas exchange elements.

A filter device includes one or more filter membranes, and a filter housing enclosing the one or more filter membranes. Each of the filter membranes includes a base membrane made of a ceramic material, and a plurality of through holes. The base membrane is coated with a coating material.

A method includes flowing an inlet solution having an inlet salinity and an inlet ion concentration from an inlet to a membrane filtration system, dynamically adjusting the salinity or ion concentration of the inlet solution in situ as the inlet solution flows to an inlet of a microfluidic cell, and determining a wettability alteration in situ while dynamically adjusting the salinity or ion concentration of the inlet solution. A system includes a fluid inlet, a microfluidic cell fluidly coupled to the fluid inlet, the microfluidic cell having a surface representative of a reservoir rock, and a membrane filtration system coupled between the microfluidic cell and the fluid inlet.

In some examples, a membrane module includes a fiber bundle. The fiber bundle includes a tubular first region and a tubular second region positioned around the tubular first region. One of the first or second regions includes hollow fibers oriented along an axis of the fiber bundle. Another of the first or second regions includes hollow fibers that are not colinear in a radial direction from the axis of the fiber bundle. A void fraction of the second region is different from a void fraction of the first region.

A particle separation multi-membrane matrix device and method are provided. The particles isolated may comprise nano-scale particles, such extracellular membrane vesicles, having a size of about 50 to about 150 nm. The vesicles are released by many different cell types, and may be efficiently isolated at high yield and purity according to the present methods from various body fluids (e.g., blood, saliva, breast milk, serum, plasma, ascites fluid, etc.). Such isolated exosome preparations may include biomarkers, such as disease biomarkers (diagnostic markers) for various disease (early stage and late stage cancers, neurological disorders (Parkinson disease, Alzheimer disease), diabetes, pancreatic diseases, renal failure, infectious diseases (HIV, tuberculosis, malaria, hepatitis)). The present methods and devices may be used to detect and monitor animals (human, livestock, companion animal) for infectious diseases, such as tuberculosis and other diseases. The methods and devices require minimal sample material (10 μl), are rapid, economical, yield highly enriched small molecule (eg, exosomes) preparations, and do not require electricity.