CS261429B1 - Bactericidal agent - Google Patents
Bactericidal agent Download PDFInfo
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- CS261429B1 CS261429B1 CS874178A CS417887A CS261429B1 CS 261429 B1 CS261429 B1 CS 261429B1 CS 874178 A CS874178 A CS 874178A CS 417887 A CS417887 A CS 417887A CS 261429 B1 CS261429 B1 CS 261429B1
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- hmt
- mother liquors
- nitrosolysis
- bactericidal agent
- formaldehyde
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Abstract
Použitie matečných lúhov z nitrolýzy hexametyléntetramínu ako prostriedku s baktericídnou aktivitou. Riešenie je možné využiť pri ochraně materiálov obsahujúcich trvale alebo přechodné vodu, napr. režných kvapalín, lepidiel, latexov, ipreplachovadiel atď.Use of mother liquors from the nitrolysis of hexamethylenetetramine as a means with bactericidal activity. The solution can be used in the protection of materials containing permanent or transient water, e.g. cutting fluids, adhesives, latexes, rinse aids, etc.
Description
261429261429
Vynález sa týká nového použitia mateč-ných lúhov z nitrozačného štiepenia hexa-ftietýléntetramínu (HMT].The present invention relates to a novel use of mother liquors from nitroso cleavage of hexaphylethylenetetramine (HMT).
Nitrozačné štiepenie HMT na cyklickénitrozoamíny z technickoekonomlckého hta-diska sa nejvýhodnejšie realizuje koffiWná-ciou kyseliny a dusitanu. Podmienky nitro-lýzy, najma kvalítatívny výběr vstupujúcichsurovin ovplyvňujú výťažok a zloženie ma-tečných lúhov.The nitrosation cleavage of HMT to cyclic nitrosoamines from the technical-economical halide is most preferably accomplished by the acidification of the acid and nitrite. Nitro-lysis conditions, especially the qualitative selection of feedstocks, affect the yield and composition of fat liquors.
Matečné luhy sú vodné roztoky anorga-nických dusičňanov, obsahujúce určitémnožstvo východiskového dusitanu, formal-dehyd, amóniové ióny, R-sol', malé množstvakyseliny mravčej, resp. mravčanov a ďalšieorganické zlúčeniny. Keď sú do nitrozolýzyhrané vodné roztoky HMT získané zahuště-ním reaikčnej zmesi zanášané množstvá N--Manichových bází, štruktúrne korešpondu-júce cukrom. Podl’a sposobu přípravy týchtoroztokov HMT sa do nitrozolýzy zanášajú di-metylamin, trimetylamín a polyoly (Cs ažC7).The mother liquors are aqueous solutions of inorganic nitrates containing a number of starting nitrite, formaldehyde, ammonium ions, R-sol, small amounts of formic acid, and the like. formates and other organic compounds. When nitrosolyzed aqueous HMT solutions are obtained by concentrating the amount of N-Manich bases clogged with the reactant mixture, they are structurally corresponding to the sugar. According to the preparation of these HMT solutions, dimethylamine, trimethylamine and polyols (Cs to C7) are introduced into nitrosolysis.
Nitrozolýza může byl zakončená neutralizá-ciou celej nitrolyzačnej zmesi alkalicky rea-gujúcou látkou. V tomto případe matečnélúhy obsahujú určitý prebytok neutralizač-nébo činidla, čo může negativné ovplyvniťkvalitu produktu a ekonomiku procesu. Priaplikácii hydroxidov alkalických ikovov salokálně zvýši teplota pri ich dávkovaní doreakčnej zmesi, čo má za následek deštruk-ciu l,5-metano-3,7-dinitrózo-l,3,5,7-tetra-aza-cyklooktánu (DNPT), a je teda potenciálnymzdrojom zníženia výťažnosti.Nitrosolysis may be terminated by neutralizing the entire nitrolysis mixture with an alkaline reactant. In this case, the masterbatches contain a certain excess of neutralizing agent, which may adversely affect product quality and process economy. The application of alkali metal hydroxides will increase the temperature of the dosing mixture in a salocal manner, resulting in destruction of 1,5-metano-3,7-dinitroso-1,3,5,7-tetra-aza-cyclooctane (DNPT), and thus, it is a potential source of yield reduction.
Alkalický hydroxid, rovnako ako aj for-maldehyd okludovaný v kryštáloch cyklic-kého nitrozamínu, resp. adsorbovaný na je-ho povrchu v priemyselných podmienkachnikdy nemožno odstrániť, čo vedie k zníže-niu jeho stálosti. Tieto nedostatky z hladis-ka stability sú riešené použitím amoniakua alkalicky reagujúcich solí zo skupinyuhličitanov·. Amoniakalizácia celej nitrozoly-začnej zmesi má význam len v,tedy, ak savznikajúce matečné lúhy recyklujú ako roz-púšťadlo surovin. Výhodnějším spůsobom za-končenia nitrozolýzy HMT je izolácia nitrozo-amínov z kyslej reakčnej zmesi s nasledu-júcou neutralizáciou, len filtračného kolá-ča.Alkaline hydroxide, as well as formaldehyde occluded in crystals of cyclic nitrosamine, respectively. adsorbed on its surface in industrial conditions can not be removed, leading to a reduction in its stability. These shortcomings in the stability of stability are solved by the use of ammonia and alkali-reacting salts of carbonates. The ammoniacalization of the entire nitrosolysis mixture is only meaningful if the absorbing mother liquors are recycled as the solvent of the raw materials. A more preferred method of ending nitrosolysis of HMT is the isolation of nitroso amines from the acidic reaction mixture followed by neutralization, only the filter cake.
Riešenie týkajúce sa izolácie niektorýchzložiek z matečných lúhov, napr. dusičnanusodného, formaldehydu, formalu a močov-noformaldehydových živíc (Cs. autor, osved-čenie č. 196 707, 206 276, 214 605, 234 447)se nevyužívajú a lúhy sa bez úžitku vypúš-tajú do životného prostredia.The solution regarding the isolation of some constituents from mother liquors, such as nitrous sodium, formaldehyde, formaldehyde and urea-formaldehyde resins (Cs. Author, certificate no. 196 707, 206 276, 214 605, 234 447) is not used and the liquors are not useful. released into the environment.
Tento problém rieši tento vynález, podláktorého sa matečné lúhy z nitrozolýzy he- xametyléntetramínu použijú ako prostriedoks bakterieídnou aktivitou.This problem is solved by the present invention, wherein mother liquors from nitrosolysis of hexamethylenetetramine are used as agents with bacterial activity.
Pokrok vynálezu sa prejavuje technický-mi účinkami, najma odstraněním problémovpri čistění vád.The advancement of the invention is manifested by technical effects, in particular by eliminating the problems of cleaning defects.
Hospodářsky pokrok riešenia sa prejavu-je znížením nákladov na dovoz, resp. výro-bu baktericídnych prostriedkov. Z hradiska spoločenského má významzlepšenie hygienických podmienok zo sú-stredeného nekontrolovaného zamorenia ži-votného prostredia odpadám.The economic progress of the solution is manifested by a reduction in the cost of imports, respectively. production of bactericidal agents. From the social fortification, the improvement of hygiene conditions from the uncontrolled contamination of the living environment is wasted.
Zloženia matečných lúhov z výroby DNPT,ktoré vychádza z HMT, dusitanu sodnéhoa kyseliny dusičné}, sa pohybuje v rozmedzí: HMT: 6,5 + 4,0 kg . m-3 = 0,58 + 0,36 %volný formaldehyd: 10,8 ± 5,7 kg . m-3 = 0,97 + 0,51 %dusičnan sodný: 130,0 ± 40,0 kg . m-3 = 11,71 + 3,60 %dusitan sodný: 16,0, + 8,0 kg . ni“3 = 1,41 + 0,72 % TMTA: 1,0 + 0,5 kg . m-3 = 0,09 + 0,04 % DNPT: max. 0,5 kg . m"3 = max. 0,045 %mravčany, polyoly (C4—C7): max. 1,5 kg . m-3 = max. 0,14 %The composition of the mother liquors from the production of DNPT, starting from HMT, sodium nitrite and nitric acid, ranges from: HMT: 6.5 + 4.0 kg. m-3 = 0.58 + 0.36% free formaldehyde: 10.8 ± 5.7 kg. m-3 = 0.97 + 0.51% sodium nitrate: 130.0 ± 40.0 kg. m-3 = 11.71 + 3.60% sodium nitrite: 16.0, + 8.0 kg. ni '3 = 1.41 + 0.72% TMTA: 1.0 + 0.5 kg. m-3 = 0.09 + 0.04% DNPT: max. 0.5 kg. m "3 = max. 0.045% formates, polyols (C4-C7): max. 1.5 kg. m-3 = max. 0.14%
Matečné lúhy z nitrozolýzy HMT je možnépoužít k ochraně režných kvapalín. Vhodnésú ako přísada do materiálov obsahujúcichtrvale alebo přechodné vodu, napr. do· lepi-diel, latexov, preplachovadiel atď. K přísluš-nému účelu je možné použit surové matečnélúhy, resp. upravené. Na přípravu účinnýchtekutin popři destilovanej a demineralizo-vanej vody je možné použit aj vodu prame-nitú, pretože soli neznižujú účinok. Aj keďsa ako rozpúšťadlo s výhodou používá voda,bez straty na účinku může túto funkciu pl-nit iné ředidlo, napr. zriedené roztoky ky-selin, zásad, amínov, tenzidov, alkoholov,regp. zmes rozpúšťadiel. Účinok matečných lúhov z nitrozolýzyHMT v zmysle vynálezu je dokumentovanýnasledujúcim príkladom, ktorý v žiadnompřípade nevylučuje možnost variability po-užitia, resp. využitia principu podstaty vy-nálezu. Příklad K dispozícii je matečný lúh z nitrozolýzyHMT, ktoré vedie k DNPT s obsahom ca 5 °/oTMTA, bez úpravy (vzorok č. 1) a po úpra-vě roztokám NažCCh z výroby cyklohexano-nu (vzorok č. 2). Zloženie vzoriek repre-zentuje tabulka č. 1.The mother liquors from nitrosolysis of HMT can be used to protect gray liquids. They are suitable as an additive to materials containing permanent or transient water, eg adhesives, latexes, flushing agents, etc. Raw materials can be used for the respective purpose. modified. For the preparation of effective liquids in distilled and demineralized water, it is also possible to use water strands because salts do not reduce the effect. Although water is preferably used as solvent, other diluents, such as dilute solutions of acids, bases, amines, surfactants, alcohols, regp. solvent mixture. The effect of the mother liquors from nitrosolysis of the HMT in the sense of the invention is documented by the following example, which does not in any case exclude the possibility of variability in the use or the use of. using the principle of the essence of the invention. EXAMPLE A mother liquor from nitrosolysis of HMT is available, which results in DNPT with a content of ca 5 ° / oTMTA, without treatment (sample No. 1) and after treatment with solutions of NaCl from the production of cyclohexane (sample no. 2). The composition of the samples is shown in Table 1.
Claims (2)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS874178A CS261429B1 (en) | 1987-06-08 | 1987-06-08 | Bactericidal agent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS874178A CS261429B1 (en) | 1987-06-08 | 1987-06-08 | Bactericidal agent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS417887A1 CS417887A1 (en) | 1988-06-15 |
| CS261429B1 true CS261429B1 (en) | 1989-02-10 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS874178A CS261429B1 (en) | 1987-06-08 | 1987-06-08 | Bactericidal agent |
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| CS (1) | CS261429B1 (en) |
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1987
- 1987-06-08 CS CS874178A patent/CS261429B1/en unknown
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| Publication number | Publication date |
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| CS417887A1 (en) | 1988-06-15 |
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