http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2747148-C1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J20-285
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J20-285
filingDate 2020-09-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d9fe3a1f3aa34c8d62328f65ff39fe02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c9ce9e6699c11670b53cc1648da60828
publicationDate 2021-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2747148-C1
titleOfInvention Method for producing selective sorbent for solid-phase extraction of pyrrolidone derivatives from biological fluids
abstract FIELD: chemistry. n SUBSTANCE: invention relates to a method for producing a selective sorbent for solid-phase extraction of pyrrolidone derivatives from biological fluids by radical polymerization of a functional monomer - methacrylic acid - when mixing. To obtain the sorbent, a combination of functional monomers is used – methacrylic acid of 0.25 g and diallylamine of 0.25 g; the structural monomer is acrylamide of 1.25 g. As a crosslinking agent, N, N´-methylene-bis-acrylamide of 0.25 g is used. Radical polymerization is carried out in the presence of a template - a pyrrolidone derivative of 0.25 g in an aqueous medium, followed by the addition of 0.1 g of ammonium persulfate, 100 mcl of N,N,N´, N´-tetramethylethylenediamine and further cooling at +8ºC. The sorbent is ground, washed with isopropyl alcohol and chloroform to remove the template from the sorbent pores, dried at room temperature to a constant mass and re-ground to a particle size of 500 mcm. n EFFECT: increased selectivity of the resulting sorbent. n 1 cl, 1 dwg, 1 tbl, 1 ex
priorityDate 2020-09-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 48.