Dissolving cellulose ester membrane

Air (total chromium) Sample collected on cellulose ester membrane filter dissolved in acid mixtures ICP-AES 1 pg/sample 98% at 2.5 pg/filter NIOSH 1994d (Method 7300)... 

Physical effects caused by polyethylene glycol bases include softening and liquefaction in mixtures with phenol, tannic acid, and salicylic acid. Discoloration of sulfonamides and dithranol can also occur and sorbitol may be precipitated from mixtures. Plastics, such as polyethylene, phenolformaldehyde, polyvinyl chloride, and cellulose-ester membranes (in filters) may be softened or dissolved by polyethylene glycols. Migration of polyethylene glycol can occur from tablet film coatings, leading to interaction with core components. 

Aldrin and lindane in air are collected over a filter bubbler, dissolved in isooctane, and injected into a GC-HECD equipped with a column containing 5% SE-30 on acid-washed DMCC Chromosorb W or equivalent (NIOSH 1984, Method 5502). The recommended airflow is 200-1000 mL/240 L. Endrin is collected over an 0.8-pm cellulose ester membrane and Chromosorb 102 extracted with toluene and analyzed by GC-ECD (NIOSH 1984, Method 5519). A column suitable for the purpose is 3% OV-1 on 100/120-mesh Chromosorb Q. 

Airborne elemental cadmium and cadmium compounds are collected on a 0.8- i.m mixed cellulose ester membrane filter (MCEF). The air filter samples are digested with concentrated nitric acid to destroy the organic matrix and dissolve the cadmium analytes. After digestion, a small amount of concentrated hydrochloric add is added to help dissolve other metals which may be present. The samples are diluted to volume with deionized water and then aspirated into the oxidizing air/acetylene flame of an atomic absorption spectrophotometer for analysis of elemental cadmium. 

As previously discussed, solvents that dissolve cellulose by derivatization may be employed for further functionahzation, e.g., esterification. Thus, cellulose has been dissolved in paraformaldehyde/DMSO and esterified, e.g., by acetic, butyric, and phthalic anhydride, as well as by unsaturated methacrylic and maleic anhydride, in the presence of pyridine, or an acetate catalyst. DS values from 0.2 to 2.0 were obtained, being higher, 2.5 for cellulose acetate. H and NMR spectroscopy have indicated that the hydroxyl group of the methy-lol chains are preferably esterified with the anhydrides. Treatment of celliflose with this solvent system, at 90 °C, with methylene diacetate or ethylene diacetate, in the presence of potassium acetate, led to cellulose acetate with a DS of 1.5. Interestingly, the reaction with acetyl chloride or activated acid is less convenient DMAc or DMF can be substituted for DMSO [215-219]. In another set of experiments, polymer with high o -celliflose content was esterified with trimethylacetic anhydride, 1,2,4-benzenetricarboylic anhydride, trimellitic anhydride, phthalic anhydride, and a pyridine catalyst. The esters were isolated after 8h of reaction at 80-100°C, or Ih at room temperature (trimellitic anhydride). These are versatile compounds with interesting elastomeric and thermoplastic properties, and can be cast as films and membranes [220]. 

Relationship Between Nodular and Rejecting Layers. Nodular formation was conceived by Maler and Scheuerman (14) and was shown to exist in the skin structure of anisotropic cellulose acetate membranes by Schultz and Asunmaa ( ), who ion etched the skin to discover an assembly of close-packed, 188 A in diameter spheres. Resting (15) has identified this kind of micellar structure in dry cellulose ester reverse osmosis membranes, and Panar, et al. (16) has identified their existence in the polyamide derivatives. Our work has shown that nodules exist in most polymeric membranes cast into a nonsolvent bath, where gelation at the interface is caused by initial depletion of solvent, as shown in Case B, which follows restricted Inward contraction of the interfacial zone. This leads to a dispersed phase of micelles within a continuous phase (designated as "polymer-poor phase") composed of a mixture of solvents, coagulant, and a dissolved fraction of the polymer. The formation of such a skin is delineated in the scheme shown in Figure 11. 

In some cases, the rate-controlling polymeric membrane is not compact but porous. Microporous membranes can be prepared by making hydrophobic polymer membranes in the presence of water-soluble materials such as polyethylene glycol), which can be subsequently removed from the polymer matrix by dissolving in aqueous solution. Cellulose esters, loosely cross-linked hydrogels and other polymers given in Table 4.2 also give rise to porous membranes. 

Several classes of polymeric materials are found to perform adequately for blood processing, including cellulose and cellulose esters, polyamides, polysulfone, and some acrylic and polycarbonate copolymers. However, commercial cellulose, used for the first membranes in the late 1940 s, remains the principal material in which hemodialysis membranes are made. Membranes are obtained by casting or spinning a dope mixture of cellulose dissolved in cuprammonium solution or by deacetylating cellulose acetate hollow fibers [121]. However, polycarbonate-polyether (PC-PE) block copolymers, in which the ratio between hydrophobic PC and hydrophilic PE blocks can be varied to modulate the mechanical properties as well as the diffusivity and permeability of the membrane, compete with cellulose in the hemodialysis market. 

Sometimes it may be necessary to use the peptides solubilized and unbound to the cellulose membrane. If it is necessary to release the peptides from the membrane, one method is to expose the entire dry membrane overnight in a glass desiccator containing ammonia gas. The strong basic environment leads to a break of the ester bond to the cellulose by forming a C-terminal amide (see Note 8). The next day, punch out the spots and transfer the discs into wells of microtiter plates (MTPs) or into vials in which you can dissolve and test the released peptides (see Note 9). If a free carboxy terminal is desired on the peptides, then do not treat the membrane with ammonia gas, punch out the spots and expose them to a basic aqueous solution, for example, ammonium hydroxide or sodium hydroxide (26). 

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