CS259282B1 - The method of determination, and the stability of the emulsion system of polymers and copolymers - Google Patents
The method of determination, and the stability of the emulsion system of polymers and copolymers Download PDFInfo
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- CS259282B1 CS259282B1 CS869427A CS942786A CS259282B1 CS 259282 B1 CS259282 B1 CS 259282B1 CS 869427 A CS869427 A CS 869427A CS 942786 A CS942786 A CS 942786A CS 259282 B1 CS259282 B1 CS 259282B1
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Abstract
Stabilita emulzného polymérneho systému vzniklého emulznou polymerizáciou alebo kopolymerizáciou akrylátov a/alebo metakrylátov sa stanovuje meraním vodivosti emulzie. Medza stability je definovaná náhlým zvýšením vodivosti.The stability of an emulsion polymer system formed by emulsion polymerization or copolymerization of acrylates and/or methacrylates is determined by measuring the conductivity of the emulsion. The stability limit is defined by a sudden increase in conductivity.
Description
Vynález sa týká spĎsobu stanovenia sta-bility emulzného systému polymérov a ko-polymérov.The invention relates to a method for determining the stability of an emulsion system of polymers and co-polymers.
Zmesný emulgačný systém sa priemyselnevyužívá k syntéze polymérov a kopolymé-rov. Ťieto zmesné emulgačné systémy po-zostávajú z emulgátorov daného homolo-gického radu, avšak v niektorých prípadochi zmesi emulgátorov rózneho typu sa uká-zali tiež vhodné [M. S. El-Aasser, T. Makga-winata, J. W. Vanderhoff, C. Pichot: Prepr.Org. Coatings Plastics Chem. 42, 44 (1980)].Z híadiska úžitkových vlastností sa poža-dujú polymérové latexy s nízkým obsahomemulgátora, pretože vysoké koncentrácie po-vrchovoaktívne] látky zvyšujú hydrofilnýcharakter polymérových filmov so slabouadhéziou a s horšími fyzikálnymi vlastnos-ťami. Inými slovami, fyzikálně vlastnosti po-lymérových filmov a stabilita polymérovýchlatexov sú funkciou koncentrácie a typu po-užitého emulgátora (J. W. Vanderhoff: J.Polym. Sci. Polym. Symp. 72, 161 (1985)].Stabilita emulzií polymérov a kopolymérovsa stanovuje meraním množstva vznikajú-ceho koagulátu prídavkom koagulačnéhočinidla. Flokulačné činidlá senzibilizujú flo-kuláciu latexových častíc, ich zhlukovaníea usadzovanie. K porovnávaniu stability jed-notlivých polymérových disperzi! sa stano-vujú počiatočné rýchlosti koagulácie.. Tentospósob stanovenia a sledovania stabilitypolymérových emulzií je značné zdíhavý aprácny. Navýše prídavok koagulačného či-nidla znehodnocuje emulziu a tým i jej ďal-šie použitie [T. Makawinata, M. S. El-Aasser,J. W. Vanderhoff, C. Pichot: Acta Polymeri-ca 32, 583 (1981)].The mixed emulsifying system is not used to synthesize polymers and copolymers. These mixed emulsifying systems consist of emulsifiers of the given homologous series, but in some cases mixtures of emulsifiers of the rhode type have also been found suitable [M. S. El-Aasser, T. Makga-winata, J. W. Vanderhoff, C. Pichot: Prepr. Coatings Plastics Chem. 42, 44 (1980)] Low-emulsifier polymer latexes are required for utility properties, since high concentrations of post-active ingredients enhance the hydrophilic character of the low-adhesion polymer films and the inferior physical properties. In other words, the physical properties of the polymer films and the stability of the polymeric ethers are a function of the concentration and the type of emulsifier used (JW Vanderhoff: J.Polym. Sci. Polym. Symp. 72, 161 (1985)] The stability of the polymer and copolymer emulsions is determined by measurement Flocculating agents sensitize the flocculation of the latex particles, their aggregation, and settling. In addition, the addition of a coagulating agent degrades the emulsion and hence its further use [T. Makawinata, MS El-Aasser, JW Vanderhoff, C. Pichot: Acta Polymeric 32, 583 (1981)].
Uvedené nevýhody v podstatnej miereodstraňuje sposob stanovenia stability e-mulzného systému polymérov a kopolymé-rov, ktorého podstata spočívá v tom, že kon-duktometricky sa meria vodivost emulzií astanoví sa medza stability emulzie, spočíva-júca v náhlom zvýšení vodivosti emulznéhosystému. Výhodou navrhovaného spósobu stanove-nia emulzného systému polymérov a kopo-lymérov je, že stanovenie je jednoduchšie,menej prácne, hospodárnejšie a umožňujesledovat stabilitu polymérových disperziívznikajúcich v priebehu polymerizačnéhoprocesu. Příklad 1The above drawbacks are substantially obviated by the method of determining the stability of the emulsion polymer and copolymer system, wherein the conductivity of the emulsions is measured and the stability of the emulsion is determined by a sudden increase in the conductivity of the emulsion system. An advantage of the proposed method of determining the emulsion system of polymers and copolymers is that the determination is simpler, less laborious, more economical, and allows the stability of the polymeric dispersants during the polymerization process to be monitored. Example 1
Do trojhrdlej reakčnej banky objemu500 ml opatrenej miešadlom, spatným chla-dičom, prívodom pre dusík, zariadením prekontinuálny odběr vzorky latexu a vodivost-nou elektrodou (OK 902) sa za kontinuál-neho přívodu dusíka vdávkuje 150 ml desti-lované] vody, 20 g metylmetakrylátu, 80 getylakrylátu, 4,5 g 97 % hmot. vodného roz-toku monopalmitán polyoxyetylén sorbitalu(Tween 40), 0,5 g 40 %-ného vodného roz-toku a-oktadecenylsulfátu sodného (Spola- pon AOS). Po· 30 minutách miešania (400 o-táčok za minútu), pri teploťe 60 °C sa přidá0,25 g persulfátu amonného (iniciátor). Vpriebehu kopolymerizácie sa odoberie 10 mllatexu k izolácii kopolyméru, množstva koa-gulátu a k stanovému stupňa konverzie. E-mulgátor, iniciátor a nezreagované mono-mery sa z latexu óídstraňujú dialýzou oprotivodě použitím dialyzačných (Visking) tru-bičiek. Takto vyčištěný kopolymérový latexsa skoaguluje v metanole okyselenom kyse-linou chlorovodíkovou na pH = 2 a koagu-láciou získaný kopolymér sa premýva vo-dou, predsuší pri teplote 60 °C po dobu 8 ho-din. Z takto získaných údajov o množstvevznikajúceho kopolyméru sa získá hodnotakonverzie [I. Čapek, J. Bartoň, E. Orolínová:Chem. Zvěsti 38, 803 (1984)]. Filtrovánímodobratej vzorky latexu sa získali údaje omnožstve koagulátu v reakčnom systéme.Pri 10 %-nej konverzii je vodivost roztoku0,5 mS . cm-1 s 0,0 g skoagulovaného ko-polyméru. Příklad 2150 ml of distilled water (20 g) are metered into a three-necked 500 ml reaction flask equipped with a stirrer, a back-cooler, a nitrogen inlet, a preconditioned latex sampling device and a conductive electrode (OK 902). methyl methacrylate, 80 gethyl acrylate, 4.5 g 97% wt. aqueous solution of monopalmitate polyoxyethylene sorbital (Tween 40), 0.5 g of a 40% aqueous solution of sodium α-octadecenyl sulfate (Part AOS). After stirring for 30 minutes (400 ° C per minute), 0.25 g of ammonium persulfate (initiator) is added at 60 ° C. During the copolymerization, 10 mllatex is taken to isolate the copolymer, the amount of coagulate, and the degree of conversion. The emulsifier, initiator and unreacted mono- mers are removed from the latex by dialysis using a dialysis tube. The purified copolymer latex is coagulated in methanol acidified with hydrochloric acid to pH = 2 and the copolymer obtained by coagulation is washed with water, dried at 60 ° C for 8 hours. From the thus obtained data on the amount of the resulting copolymer, the conversion value is obtained [I. Čapek, J. Bartoň, E. Orolínová: Chem. Rumors 38, 803 (1984)]. By filtering a sample of the latex, the amount of coagulum in the reaction system was obtained. For a 10% conversion, the conductivity of the solution was 0.5 mS. cm-1 with 0.0 g of coagulated co-polymer. Example 2
Postupuje sa ako v příklade 1 s tým roz-dielom, že sa meria vodivost latexu a stano-ví množstvo koagulátu pri 40 %-nej konver-zii. Vodivost kopolymérového latexu je0,5 mS . cm-1 a latex obsahuje 0,0 g skoagu-lovaného: kopolyméru. Příklad 3The procedure is as in Example 1, except that the conductivity of the latex is measured and the amount of coagulum is determined at 40% conversion. The conductivity of the copolymer latex is 0.5 mS. cm-1 and the latex contains 0.0 g of coagulated copolymer. Example 3
Postupuje sa ako v příklade 1 s tým roz-dielom, že sa meria vodivost latexu a sta-noví množstvo koagulátu pri 45 %-nej kon-verzii. Vodivost kopolymérového latexu je0,6 mS . cm-1 a latex obsahuje 0,1 g skoagu-lovaného kopolyméru. Údaje indikujú medzustability kopolymérového latexu. Příklad 4The procedure is as in Example 1, except that the conductivity of the latex is measured and the amount of coagulum is fixed at a 45% conversion. The conductivity of the copolymer latex is 0.6 mS. cm-1 and the latex contains 0.1 g of coagulated copolymer. The data indicate the interstability of the copolymer latex. Example 4
Postupuje sa ako v příklade 1 s tým roiz-dielom, že sa meria vodivost latexu a sta-noví množstvo koagulátu pri 60 %-nej kon-verzii. Vodivost latexu je 1,3 mS. cm“1 alatex obsahuje 1,0 g skoagulovaného kopo-lyméru. Příklad 5The procedure is as in Example 1, with the exception that the conductivity of the latex is measured and the amount of coagulum is fixed at 60%. The latex conductivity is 1.3 mS. cm '1 alatex contains 1.0 g of coagulated copolymer. Example 5
Postupuje sa ako v příklade 1 s tým roz-dielom, že sa meria vodivost latexu a sta-noví množstvo koagulátu pri 80 %-nej kon-verzii. Vodivost latexu je 2,0 mS . _1 a la-tex obsahuje 2,0 g skoagulovaného kopo-lyméru. Příklad 6The procedure is as in Example 1, except that the conductivity of the latex is measured and the amount of coagulum is fixed at 80% conversion. The latex conductivity is 2.0 mS. 1 and 1a-tex contains 2.0 g of the coagulated copolymer. Example 6
Postupuje sa ako v příklade 1 s tým roz- dielom, že sa meria vodivost latexu a sta- noví množstvo koagulátu pri 30 %-nej kon-The procedure is as in Example 1, except that the conductivity of the latex is measured and the amount of coagulum determined at 30% by weight.
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| CS869427A CS259282B1 (en) | 1986-12-17 | 1986-12-17 | The method of determination, and the stability of the emulsion system of polymers and copolymers |
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| CS869427A CS259282B1 (en) | 1986-12-17 | 1986-12-17 | The method of determination, and the stability of the emulsion system of polymers and copolymers |
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| CS942786A1 CS942786A1 (en) | 1988-02-15 |
| CS259282B1 true CS259282B1 (en) | 1988-10-14 |
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