CS219105B1 - Lubricant with anticorrosion effects for electromechanical products - Google Patents

Lubricant with anticorrosion effects for electromechanical products Download PDF

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CS219105B1
CS219105B1 CS807351A CS735180A CS219105B1 CS 219105 B1 CS219105 B1 CS 219105B1 CS 807351 A CS807351 A CS 807351A CS 735180 A CS735180 A CS 735180A CS 219105 B1 CS219105 B1 CS 219105B1
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lubricant
corrosion
additive
weight
electromechanical components
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CS807351A
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Czech (cs)
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Ivan Zehle
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Ivan Zehle
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Priority to CS807351A priority Critical patent/CS219105B1/en
Priority to DD81233448A priority patent/DD210549A3/en
Priority to FR8118343A priority patent/FR2493335A1/en
Priority to GB8131872A priority patent/GB2086418B/en
Priority to CH6893/81A priority patent/CH648589A5/en
Priority to DE19813143185 priority patent/DE3143185A1/en
Priority to HU359081A priority patent/HU188558B/en
Publication of CS219105B1 publication Critical patent/CS219105B1/en

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    • C10M133/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
    • C10M133/38Heterocyclic nitrogen compounds
    • C10M133/44Five-membered ring containing nitrogen and carbon only
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    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/14Synthetic waxes, e.g. polythene waxes
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    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/16Paraffin waxes; Petrolatum, e.g. slack wax
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
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    • C10M2207/28Esters
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    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2215/042Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
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    • C10M2215/22Heterocyclic nitrogen compounds
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    • C10M2215/226Morpholines
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    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/104Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
    • C10M2219/108Phenothiazine
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    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/12Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
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    • C10N2040/30Refrigerators lubricants or compressors lubricants
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    • C10N2040/38Conveyors or chain belts
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  • Chemical & Material Sciences (AREA)
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  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)

Abstract

Lubricant having anticorrosive properties for electromechanical components comprises a C20-35 ester of a dicarboxylic acid and 1 x 10<-4> to 10 g./l. of at least one pyrazolidine of formula <IMAGE> where R1 to 6 are C10 alkyl or aryl, NH2 or H. The lubricant enables a reduction of the thickness of coatings of precious metal on their contact surfaces, improving the resistivity to corrosion and prolonging their life time.

Description

Vynález se týká . složení · lubrikantu pro elektromechanické součástky s antikorozními účinky, který umožňuje snížení tloušťky povlaku drahého kovu na . kontaktních plochách, značně zvyšuje korozní odolnost těchto součástek a prodlužuje jejich ' životnost tím, že omezuje mechanické opotřebení.The invention relates. the composition of a lubricant for electromechanical components with anticorrosive effects, which allows reducing the coating thickness of the precious metal to. contact surfaces greatly increases the corrosion resistance of these components and extends their service life by reducing mechanical wear.

Za elektromechanickou součástku je zde považována součástka využívaná pro spínání, spojování & rozpojování elektrického obvodu. Vykonává tedy vždy jistou mechanickou funkci a přenáší přitom elektrický proud, například konektor nebo přepínač.An electromechanical component here is considered to be a component used for switching, connecting & disconnecting an electrical circuit. Thus, it always performs a mechanical function and transmits electrical current, for example a connector or a switch.

V praxi je znáimo použití různých látek snižujících tření a omezujících korozi elektromechanických součástek. Využívá se k tomu obvykle minerálních olejů, solí a esterů mastných kyselin a dikariboxylových kyselin atd. Tyto· látky se obvykle kombinují s látkami slabil· ziačními, případně· s látkami! s antikorozním působením. Ke stabilizaci se používá obvykle látek typu fencthiazinu nebo substituovaného fenolu. Tyto směsi však většinou působí pouze mechanicky a nemají antikorozní účinky za' podmínek zkoušení elektromechanických součástek. To platí i o radě látek, které se v jiných oblastech . . úspěšně. · používají Jako .. .inhibitory koroze.In practice, it is known to use a variety of friction reducing and corrosion reducing agents for electromechanical components. Usually mineral oils, salts and esters of fatty acids and dicariboxylic acids, etc. are used for this purpose. These substances are usually combined with weakening substances or substances! with anticorrosive effect. Usually, the phenothiazine or substituted phenol type is used for stabilization. However, these mixtures generally act only mechanically and do not have corrosion effects under the test conditions of electromechanical components. This also applies to a number of substances that are in other areas. . successfully. Use as corrosion inhibitors.

Měření ukázala, že látky obvykle používané ke stabilizaci lubrikantů ' ' i · některé látky všeobecně používané jako inhibitory koroze naopak korozi silně urychlují, zejména při provádění korozních zkoušek s čistými látkami bez přítomnosti vlastních lubrlikantů, které jejich korozní působení do značné míry překrývají a to se potom projeví až za extrémních podmínek. Dobrou stabilitu lubrikantu je dle tohoto vynálezu zabezpečit i ve směsích obsahujících pouze látky, které mají za podmínek zkoušení a použití elektromechanických součástek výrazně inhťbiční účinky na korozi.Measurements have shown that substances commonly used to stabilize lubricants and some substances commonly used as corrosion inhibitors, on the contrary, strongly accelerate corrosion, especially when conducting corrosion tests with pure substances without the presence of intrinsic lubricants which largely overlap their corrosion action, then manifest under extreme conditions. According to the invention, good lubricant stability is also assured in mixtures containing only substances which, under the conditions of testing and use of electromechanical components, have markedly inhibitory corrosion effects.

Nevýhody dříve používaných lubrikantů jsou odstraněny směsí podle vynálezu obsahující pouze látky s význačným antikorozním působením, která míi přitom dobrou stabilitu a je zvláště vhodná pro elektromechanické součástky pokryté zcela nebo zčásti povlakem kovu ušlechtilejšího, než je základní materiál součástky, nebo 'materiál použité mezivrstvy. Měření prokázala, že zejména kombinací dvou inhibitorů koroze různých typů se podstatně zvyšuje antikorozní působení.The disadvantages of the lubricants previously used are eliminated by the composition according to the invention containing only substances with a significant anti-corrosion effect, which at the same time has good stability and is particularly suitable for electromechanical parts covered wholly or partially with a nobler metal than the base material or interlayer material. Measurements have shown that especially by combining two corrosion inhibitors of different types, the anticorrosive effect is substantially increased.

Lubrikainit je·v podstatě tvořen esterem dikarboxylové kyseliny, která má 5 až 12 atomů uhlíku v molekule -a · její ester celkem 20 až 28 atomů uhlíku v molekule, s přídavkem látky. . ze skupiny . pyrazolidcnu . v . .koncentraci 0,01 až 1 % hmot., která vyhovuje jedné ze tří možných struktur:Lubricinite consists essentially of a dicarboxylic acid ester having 5 to 12 carbon atoms in the molecule and its ester having a total of 20 to 28 carbon atoms in the molecule, with the addition of a substance. . from the group. pyrazolidine. v. a concentration of 0,01 to 1% by weight, which satisfies one of the three possible structures:

kde Ri až Rs je metyl nebo fenyl, nebo H.wherein R 1 to R 5 is methyl or phenyl, or H.

Směs může .dále obsahovat přísadu parafinu, který mění mechanické vlastnosti lubrikaintu a. přísadu benzotriazolu nebo tolyltriazolu.The composition may further comprise an additive of paraffin which alters the mechanical properties of the lubricant and an additive of benzotriazole or tolyltriazole.

K praktickému odzkoušení lubrikantů podle vynálezu byly připraveny směsi o složení uvedeném v příkladech 1 až 9. Píro porovnání antikorozních účinků byly připraveny další směsi obsahující často používané antloxidanty (příklad 10 .až 11), v dalších směsích . jsou tyto látky v kombinaci s jinými látkami často používanými jako inhibitory koroze (příklad 12 až 13).For practical testing of the lubricants of the invention, compositions having the compositions shown in Examples 1 to 9 were prepared. Further compositions containing frequently used antloxidants (Examples 10-11) were prepared for comparing the anticorrosive effects, in other compositions. they are in combination with other agents frequently used as corrosion inhibitors (Examples 12-13).

Příklad 1 di-3,5,5 triímetyl azelát 84% hmot.EXAMPLE 1 Di-3,5,5 Triethyl Azelate 84 wt.

(1 -fenyl^-pyrazolidon 1 % hmot parafin 15 % hmot.(1-phenyl-4-pyrazolidone 1 wt.% Paraffin 15 wt.

dioktylsebakát 98,9 % --metyl^-pyrazolidon 1 · % tolyKriazol 0,1 %dioctyl sebacate 98.9% - methyl-4-pyrazolidone 1 ·% tolyCriazole 0.1%

Příklad 3Example 3

Bis-2~-eh'ylliexyladipát 93,9 % l-fenyl-5-;metyl-3-pyrazxlidon 1 % benzotriazol 0,1 % parafin . 5 %Bis-2-methylhexyl adipate 93.9% 1-phenyl-5-methyl-3-pyrazxlidone 1% benzotriazole 0.1% paraffin. 5%

P r í k 1 a! -1 4 d1-3,5,5-trimethylhexyl azelát 99 % l-fenyl-S-imetyl^-pyrazolidon 1 % benzotriazol 10_4 одExample 1! -1 4 d -1-3,5,5-trimethylhexyl azelate 99% 1-phenyl-S-imethyl-4-pyrazolidone 1% benzotriazole 10 _ 4 од

Příklad 5 dioktylsebakát 99,5 %Example 5 Dioctyl sebacate 99.5%

5-metyl-3-pyrazo>lidoin 0,5 %5-methyl-3-pyrazole lidoin 0.5%

Příklad 6 dioktylsebakát 99,99 °/oExample 6 Dioctyl sebacate 99.99%

5-'mietyl-3-pyrazolidon 0,01 °/o5-Methyl-3-pyrazolidone 0.01%

Příklad 7 di-3,5,5-trimethylhexyl azelát 99,49 % l-feinyl-3-pyrazolidon 0,01 % tolyiltriazol 0,5 %Example 7 di-3,5,5-trimethylhexyl azelate 99.49% 1-phenynyl-3-pyrazolidone 0.01% tolyiltriazole 0.5%

Příklad 8 •di-3,5,5 tirimiethythexyl azelát 99 % 5-Tnietyl-3-py>r>a!ZOlidon 1 % bcinizo.rjazol 10r 4 %EXAMPLE 8 • Di-3,5,5-thiimethylethexyl azelate 99% 5-Triethyl-3-pyrazolone 1% bcinisoljazol 10% 4 %

P ř í к 1 a d 9 ,ďoktyl dcdekandiát 59 % l-fenyl-3-pyrazolidon 1 % parafin 40 %EXAMPLE 1, Doctyl dcdecandiate 59% 1-Phenyl-3-pyrazolidone 1% Paraffin 40%

Příklad 10 dibktyliadipált 58 %Example 10 dibktyliadipalt 58%

2,6i-dite'rc.butyl-4-'meitylfenol 1 % l-fenyl-3-pyrazolidoin 1 % parafin 40 °/o2,6-Di-tert-butyl-4-methyl-phenol 1% 1-phenyl-3-pyrazolidoin 1% paraffin 40%

Příklad 11 dioktyladipát 93 %Example 11 dioctyl adipate 93%

2.6- dite|rc.butyl-4-metylfenol 1 °/o l-fenyl-3-py'razol:don 1 % parafin 5 %2.6- child | tert-butyl-4-methylphenol 1% -1-phenyl-3-pyrazole: don 1% paraffin 5%

Příklad 12 dioktylsebakát 98 %Example 12 Dioctyl sebacate 98%

2.6- diiterc.butyl-4metyIfenol .1 % oktadecylamin 1 °/o2,6-di-tert-butyl-4-methylphenol. 1% octadecylamine 1% w / w

Příklad 13 di-3,5,5-tirii'met|liylhexyl.azelát 98 % fcnothiazin 1 % trietanioilamin 1 %Example 13 di-3,5,5-tirii'met | liylhexyl azlate 98% Phenothiazine 1% triethanioilamin 1%

Ve všech uvedených příkladech bylo složení zaokrouhlováno na setiny procenta.In all the examples, the composition was rounded to hundredths of a percent.

Všechny připravené směsi byly zkoušeny za stejných podmínek. Jako kritérium korozní lodoiinosti bylo použdo .měření přechodového odporu kontaktů po zkoušce v sirovodíkové atmosféře, která je obvyklou zkouškou píro tento druh součástek. Lubrikanty byly na kontakty naneseny ze 4% roztoku v xylenu. Pro zkoušky bylo použito kontaktů s vnější kontaktní plochou nepřímého řadového konektoru s kruhovými kontakty s přibližně 0,,25 mikrometry zlata v kontaktní části. Kontakty byly po usušení při teplotě 60 °C namontovány do příslušných tělísek. Odpovídající zásuvky se zlacenými kontakty byly použity pouze pro měření .a nebyly podrobeny korozní zkoušce. Po změření počátečního· přechodového odporu byly vdlice vlaženy do sirovodíku o koncentraci 1 % objemové při relativní vlhkosti 95 % o tepjoíš 25 °C na dobu 48 hodin a opět byl změřen přechodový odpor.All prepared mixtures were tested under the same conditions. As a corrosion test, a contact resistance measurement after the test in a hydrogen sulphide atmosphere, which is the usual test for this kind of components, was used. Lubricants were applied to the contacts from a 4% solution in xylene. Contacts with an outer contact surface of an indirect row connector with circular contacts with approximately 0.25 micrometers of gold in the contact portion were used for the tests. The contacts were mounted in the appropriate bodies after drying at 60 ° C. Corresponding gold-plated contact sockets were used for measurements only and were not subjected to corrosion testing. After measuring the initial transient resistance, the wells were pulled into 1% by volume hydrogen sulfide at 95% relative humidity at 25 ° C for 48 hours and the transient resistance was again measured.

.Pro každý vzorek by i o použito 30 kontaktů a z průměrných naměřených hodnot bylo vypočteno procentické zvýšení přechodového odporu po korozní zkoušce. Každý kontakt byl měřen 5krát. Výsledky jsou obsaženy v tabulce 1. Z výsledků je patrno, že lubrikanty dle vynálezu (1 až 9) poskytují nejlepší výsledky. Pro srovnání byla provedena stejná zkouška i s kontakty 'bez lubrikantu, v tabulce je tato skupina označena jako „0“’.30 contacts would be used for each sample and the percent increase in transient resistance after the corrosion test was calculated from the average values measured. Each contact was measured 5 times. The results are shown in Table 1. The results show that the lubricants of the invention (1 to 9) provide the best results. For comparison, the same test was performed with 'no lubricant contacts', in the table, this group is marked '0'.

К demonstraci dlouhodobé stability lubrikiantu dle tohoto vynálezu byla stejná zkouška provedena i po dlouhodobém zahřívání (56 dní) kontaktů opatřených lubrikanty na teplotu 100 °C. Výsledky jsou rovněž v tabulce a jsou v dobré shodě s předešlými, lubrikanty podle vynálezu opět poskytují nejlepší antikorozní ochranu. Hodnoty zvýšení přechodového odporu jsou ve všech případech poněkud vyšší vlivem vyšší náročnosti provedené zkoušky.To demonstrate the long-term stability of the lubricant of the present invention, the same test was performed after long-term heating (56 days) of the lubricated contacts to 100 ° C. The results are also in the table and are in good agreement with the foregoing, the lubricants of the invention again provide the best corrosion protection. The values of increase of the transient resistance are in all cases somewhat higher due to higher demands of the performed test.

Lubrikant 0Lubricant 0

Tabulka 1Table 1

5 6 7 ld 11.5 6 7 ld

1313

Ki (%) 84 27 18 11 15 42 51 38 38 25 128 68 92 140Ki% 84 27 18 11 15 42 51 38 38 25 128 68 92 140

K2 ('%) 121 35 23 20 23 54 62 48 51 31 181 111 Ϊ51 158K 2 ('%) 121 35 23 20 23 54 62 48 51 31 181 111 51 51 158

Ki je zvýšení přechodového odporu v pro- Кг je zvýšení přechodového odporu po centech po 48 hodinách v sirovodíkové at- 56 dnech zahřívání na 100 °C a 48 hodinách mosféře v sirovodíkové atmosféře vyjádřené v procentech.Ki is the increase in transient resistance in pro- cog is the increase in transient resistance in cents after 48 hours in hydrogen sulphide and 56 days of heating to 100 ° C and 48 hours in hydrogen sulphide atmosphere expressed as a percentage.

Claims (3)

1. Luibrikaint pro elektromechanické součástky s antikorozními účinky omezující podstatně jejich korozi a 'mechanické opotřebení, vyznačený tím, že je tvořen esterem dikairboxyloivé kyseliny, která má 6 až 12 atomů uhlíku v molekule a její- ester celVYNALEZU kem 22 až 28 «atomů uhlíku v molekule s přísadou 0,01 až 1 % hmot, vztaženo na celkovou hmotnost lubrikantu, sloučeniny ze skupiny pyrazolidonu nebo jejich směsi, jejichž složení vyhovuje jedné ze tří možných struktur:Luibrikaint for electromechanical components with anticorrosive effects substantially reducing their corrosion and mechanical wear, characterized in that it consists of a dicarboxylic acid ester having from 6 to 12 carbon atoms per molecule and its ester from 22 to 28 «carbon atoms in the molecule a molecule with an additive of 0.01 to 1% by weight, based on the total weight of the lubricant, of a compound of the pyrazolidone group or a mixture thereof, the composition of which conforms to one of three possible structures: kde Ri až R6 je metyl nebo fenyl nebo H, a případně obsahuje přísadu parafinu, benzo·triazolu nebo tolyltriazolu.wherein R 1 to R 6 is methyl or phenyl or H, and optionally comprises an additive of paraffin, benzotriazole or tolyltriazole. 2. Lubrikant pro elektromechanické součástky podle bodu 1 . vyznačený tím, že obsahuje přísadu parafinu s bodem měknutí nad 40' °C v množství do 40 % hmot., vztaženo na celkovou trniotnost lubrikantu.2. Lubricant for electromechanical components according to item 1. characterized in that it comprises a paraffin additive having a softening point above 40 ° C in an amount of up to 40% by weight, based on the total shear life of the lubricant. 3. Lubrikant pro elektromechanické součástky podle bodu 1 nebo 2 vyznačený tím, že obsahuje přísadu benzotriazolu nebo tolylťriazolu v množství 1Ό-4 &ž 0„5 % hmot., vztaženo na celkovou hmotnost' lubrikantu.3. Lubricant for electromechanical components according to claim 1 or 2, characterized in that it contains an additive of benzotriazole or tolyltriazole in an amount of 1 - 4 to 0 - 5% by weight, based on the total weight of the lubricant.
CS807351A 1980-10-30 1980-10-30 Lubricant with anticorrosion effects for electromechanical products CS219105B1 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
CS807351A CS219105B1 (en) 1980-10-30 1980-10-30 Lubricant with anticorrosion effects for electromechanical products
DD81233448A DD210549A3 (en) 1980-10-30 1981-09-21 FAT FOR ELECTROMECHANIC PARTS WITH ANTI-STRENGTH EFFECT
FR8118343A FR2493335A1 (en) 1980-10-30 1981-09-29 LUBRICANT FOR ELECTROMECHANICAL ELEMENTS WITH ANTI-CORROSION ACTION
GB8131872A GB2086418B (en) 1980-10-30 1981-10-22 Lubricant having anticorrosive properties for electro-mechanical components
CH6893/81A CH648589A5 (en) 1980-10-30 1981-10-28 LUBRICANTS FOR ELECTROMECHANICAL COMPONENTS WITH ANTICORROSIVE EFFECT.
DE19813143185 DE3143185A1 (en) 1980-10-30 1981-10-30 LUBRICANTS WITH ANTICORROSIVE EFFECT FOR ELECTROMECHANICAL COMPONENTS
HU359081A HU188558B (en) 1980-10-30 1981-11-30 Composition of protection of corrosion for sparing electric contacts

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CS807351A CS219105B1 (en) 1980-10-30 1980-10-30 Lubricant with anticorrosion effects for electromechanical products

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CS219105B1 true CS219105B1 (en) 1983-02-25

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CH (1) CH648589A5 (en)
CS (1) CS219105B1 (en)
DD (1) DD210549A3 (en)
DE (1) DE3143185A1 (en)
FR (1) FR2493335A1 (en)
GB (1) GB2086418B (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4529531A (en) * 1984-02-22 1985-07-16 Stauffer Chemical Company Electrical contact lubricant composition and method of lubrication
IL125467A (en) * 1996-05-10 2008-12-29 Shishiai Kk Energy conversion composition
US10998730B1 (en) 2019-04-26 2021-05-04 NeoVolta, Inc. Adaptive solar power battery storage system

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GB2086418B (en) 1984-03-21
CH648589A5 (en) 1985-03-29
DD210549A3 (en) 1984-06-13
FR2493335A1 (en) 1982-05-07
DE3143185A1 (en) 1982-06-16
GB2086418A (en) 1982-05-12

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