B01D65/109

Method and arrangement for determining at least one pore-related parameter of a porous structure

In the present invention, a method for determining at least one pore-related parameter of a porous structure is provided. In a preferred embodiment, an enhanced evapoporometry (EP) technique is provided to determine pore size distribution of continuous pores of a porous structure. In this enhanced EP technique, a volatile liquid, such as isopropoyl alcohol or water, is supplied to one side of a porous structure in order to enable the volatile liquid to penetrate and saturate the porous structure through capillary force. Thereafter, an immiscible non-volatile liquid, such as glycerol, mineral oils, silicon oils or hydrophilic ionic liquid, is supplied to the one side of the porous structure. As the volatile liquid evaporates progressively from the filled pores, the emptied pores may be immediately filled by the non-volatile liquid drawn upwards by capillary action. This prevents formation of a t-layer formed from the adsorption of vapour emanating from the volatile liquid that is used to saturate the pores.

ZWITTERION-FUNCTIONALIZED MULTICOMPONENT COPOLYMERS AND ASSOCIATED POLYMER BLENDS AND MEMBRANES

Multicomponent copolymers including two or more types of repeat units is presented. In one example, the multicomponent copolymer includes at least one repeat unit AC having a structure (I), at least one repeat unit DC having a structure (II), and at least one repeat unit BC having a structure (III) or (V). The multicomponent copolymer may be cross-linked via a cross-linking agent. A polymer blend including the multicomponent copolymer or a cross-linked copolymer and a second polymer is also provided. The multicomponent copolymer may be a random or a block copolymer. The structural units of the multicomponent copolymers provide improved, tunable properties, such as improved biocompatibility and hydrophilicity, protein fouling, and mechanical properties, to the copolymers and/or the membranes fabricated from the copolymers.

Method and apparatus for real-time direct membrane monitoring

A membrane surface monitoring system (MSM) and membrane surface monitoring cell for direct and unambiguous detection of membrane surface fouling and mineral scaling. The system includes a membrane surface monitoring system cell, a control valve, a retentate flow meter/transmitter and a controller. The MSM cell has a visually-observable membrane, an edge-lit light guide, an edge illumination light source, a retentate module, and a permeate module. A pressurized inlet stream is fed into the MSM cell. The feed contacts a membrane sheet, leading to membrane-based separation operation to produce retentate and permeate streams. The MSM cell integrates surface illumination and imaging components to allow direct real-time visualization and spectral imaging of the membrane surface in real time. The pressure on the feed-side of the MSM cells is approximately that of the membrane plant element being monitored such that the plant control system can adjust plant operating conditions.

Method for analyzing particle accumulation on a filter membrane

Methods for analyzing an accumulation of particles on a filter membrane involve analyzing comprise the particle accumulation in an optical analysis system using a light microscope, and then analyzing the particle accumulation in an SEM-EDX analysis system using a scanning electron microscope and energy-dispersive X-ray spectroscopy. In order to simplify and accelerate the testing of the filter membrane both in the optical analysis system and in the SEM-EDX system, the filter membrane is subject to a preparation which includes: (i) fixing the particles to the filter membrane, (ii) coating the particle accumulation with an electrically conductive coating which is produced from a conductivity solution that contains an ionic liquid, and (iii) holding the filter membrane flat or pulling the filter membrane taut.

Method and Apparatus for Real-Time Direct Membrane Monitoring

A membrane surface monitoring system (MSM) and membrane surface monitoring cell for direct and unambiguous detection of membrane surface fouling and mineral scaling. The system includes a membrane surface monitoring system cell, a control valve, a retentate flow meter/transmitter and a controller. The MSM cell has a visually-observable membrane, an edge-lit light guide, an edge illumination light source, a retentate module, and a permeate module. A pressurized inlet stream is fed into the MSM cell. The feed contacts a membrane sheet, leading to membrane-based separation operation to produce retentate and permeate streams. The MSM cell integrates surface illumination and imaging components to allow direct real-time visualization and spectral imaging of the membrane surface in real time. The pressure on the feed-side of the MSM cells is approximately that of the membrane plant element being monitored such that the plant control system can adjust plant operating conditions.

Zwitterion-functionalized multicomponent copolymers and associated polymer blends and membranes

Multicomponent copolymers including two or more types of repeat units is presented. In one example, the multicomponent copolymer includes at least one repeat unit AC having a structure (I), at least one repeat unit DC having a structure (II), and at least one repeat unit BC having a structure (III) or (V). The multicomponent copolymer may be cross-linked via a cross-linking agent. A polymer blend including the multicomponent copolymer or a cross-linked copolymer and a second polymer is also provided. The multicomponent copolymer may be a random or a block copolymer. The structural units of the multicomponent copolymers provide improved, tunable properties, such as improved biocompatibility and hydrophilicity, protein fouling, and mechanical properties, to the copolymers and/or the membranes fabricated from the copolymers.

SYSTEM AND METHOD FOR DIALYZER EVALUATION
20200353145 · 2020-11-12 ·

Embodiments of the disclosure provide a method for evaluating dialyzers used in different medical applications (e.g., hemodialysis). Red blood cell volume lost in a dialyzer is monitored by obtaining blood flowrate measurements and hematocrit measurements at input ports and output ports of the dialyzer. The flowrate and hematocrit measurements are used to determine an accumulation of red cell blood volume in the dialyzer. The measurements may be obtained in a lab environment with an in-vitro blood source or may be obtained in a clinical setting with an in-vivo blood source from a patient.

Method and Apparatus for Real-Time Direct Membrane Monitoring

A membrane surface monitoring system (MSM) and membrane surface monitoring cell for direct and unambiguous detection of membrane surface fouling and mineral scaling. The system includes a membrane surface monitoring system cell, a control valve, a retentate flow meter/transmitter and a controller. The MSM cell has a visually-observable membrane, an edge-lit light guide, an edge illumination light source, a retentate module, and a permeate module. A pressurized inlet stream is fed into the MSM cell. The feed contacts a membrane sheet, leading to membrane-based separation operation to produce retentate and permeate streams. The MSM cell integrates surface illumination and imaging components to allow direct real-time visualization and spectral imaging of the membrane surface in real time. The pressure on the feed-side of the MSM cells is approximately that of the membrane plant element being monitored such that the plant control system can adjust plant operating conditions.

System and method for dialyzer evaluation

Embodiments of the disclosure provide a method for evaluating dialyzers used in different medical applications (e.g., hemodialysis). Red blood cell volume lost in a dialyzer is monitored by obtaining blood flowrate measurements and hematocrit measurements at input ports and output ports of the dialyzer. The flowrate and hematocrit measurements are used to determine an accumulation of red cell blood volume in the dialyzer. The measurements may be obtained in a lab environment with an in-vitro blood source or may be obtained in a clinical setting with an in-vivo blood source from a patient.

Method for blowing free a wetted hydrophobic filter, and device for carrying out the method

A method for clearing a wetted hydrophobic filter includes a first step in which the air permeability of the hydrophobic filter is monitored, and a second step in which the hydrophobic filter is cleared by means of a connected air pump, if it is detected that the hydrophobic filter is clogged. An apparatus for performing this method includes a pressure sensor and an air pump connected to an air separation chamber via a conduit, and a control and monitoring unit configured to actuate the air pump in order to clear the hydrophobic filter.