U.S. patent application number 11/955949 was filed with the patent office on 2008-07-10 for low-friction sliding mechanism.
This patent application is currently assigned to NISSAN MOTOR CO., LTD.. Invention is credited to Takahiro Hamada, Makoto Kano, Shozaburo KONISHI, Yutaka Mabuchi, Shigeki Takeshima, Kenji Tsushima, Yoshiteru Yasuda.
Application Number | 20080167206 11/955949 |
Document ID | / |
Family ID | 32110662 |
Filed Date | 2008-07-10 |
United States Patent
Application |
20080167206 |
Kind Code |
A1 |
KONISHI; Shozaburo ; et
al. |
July 10, 2008 |
LOW-FRICTION SLIDING MECHANISM
Abstract
A low-friction sliding mechanism includes first and second
sliding members having respective sliding surfaces slidable
relative to each other and a lubricant applied to the sliding
surfaces of the first and second sliding members. At least the
sliding surface of the first sliding member is made of a
diamond-like carbon material, and at least the sliding surface of
the second sliding member is made of either an aluminum-based alloy
material, a magnesium-based alloy material or a diamond-like carbon
material. The lubricant contains a base oil and at least one of an
ashless fatty-ester friction modifier and an ashless
aliphatic-amine friction modifier.
Inventors: |
KONISHI; Shozaburo;
(Yokohama, JP) ; Kano; Makoto; (Yokohama, JP)
; Yasuda; Yoshiteru; (Yokohama, JP) ; Mabuchi;
Yutaka; (Yokohama, JP) ; Hamada; Takahiro;
(Yokohama, JP) ; Takeshima; Shigeki; (Yokohama,
JP) ; Tsushima; Kenji; (Yokohama, JP) |
Correspondence
Address: |
FOLEY AND LARDNER LLP;SUITE 500
3000 K STREET NW
WASHINGTON
DC
20007
US
|
Assignee: |
NISSAN MOTOR CO., LTD.
NIPPON OIL CORPORATION
|
Family ID: |
32110662 |
Appl. No.: |
11/955949 |
Filed: |
December 13, 2007 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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11123016 |
May 6, 2005 |
7322749 |
|
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11955949 |
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|
10692853 |
Oct 27, 2003 |
6969198 |
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11123016 |
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Current U.S.
Class: |
508/103 ;
123/196R; 508/109 |
Current CPC
Class: |
C10M 2205/0285 20130101;
C10M 163/00 20130101; C10N 2010/04 20130101; C10N 2010/12 20130101;
F16C 33/12 20130101; F16C 33/04 20130101; C10M 2223/045 20130101;
C10M 2215/042 20130101; F16C 2206/04 20130101; F16C 2204/26
20130101; C10N 2040/04 20130101; C10M 2207/028 20130101; F16C
33/109 20130101; F16C 33/10 20130101; C10M 2219/046 20130101; C10N
2040/18 20130101; C10M 2203/1006 20130101; C10M 2219/068 20130101;
C10N 2040/25 20130101; C10M 2207/289 20130101; F16C 2204/20
20130101; C10M 2215/28 20130101 |
Class at
Publication: |
508/103 ;
508/109; 123/196.R |
International
Class: |
F16C 33/12 20060101
F16C033/12; F01M 11/00 20060101 F01M011/00 |
Foreign Application Data
Date |
Code |
Application Number |
Nov 6, 2002 |
JP |
2002-322322 |
Aug 11, 2003 |
JP |
2003-207056 |
Aug 21, 2003 |
JP |
2003-208193 |
Claims
1. A low-friction sliding mechanism, comprising: a first sliding
member having a sliding surface, at least the sliding surface of
the first sliding member comprising a diamond-like carbon material;
a second sliding member having a sliding surface slidable relative
to the sliding surface of the first sliding member, and a lubricant
applied to the sliding surfaces of the first and second sliding
members, the lubricant comprising at least one of an ashless
fatty-ester friction modifier and an ashless aliphatic-amine
friction modifier.
2. A low-friction sliding mechanism according to claim 1, wherein
the diamond-like carbon material of the first sliding member is
hydrogen-free amorphous carbon.
3. A low-friction sliding mechanism according to claim 15, wherein
the aluminum-based alloy material of the second sliding member is a
hypoeutectic or hypereutectic aluminum alloy containing 4 to 20% by
mass silicon and 1.0 to 5.0% by mass copper.
4. A low-friction sliding mechanism according to claim 15, wherein
the magnesium-based alloy material of the second sliding member
comprises at least one alloy selected from the group consisting of
magnesium-aluminum-zinc alloys, magnesium-aluminum-rare earth metal
alloys, magnesium-aluminum-calcium alloys,
magnesium-zinc-aluminum-calcium alloys,
magnesium-aluminum-calcium-rare earth metal alloys,
magnesium-aluminum-strontium alloys, magnesium-aluminum-silicon
alloys, magnesium-rare earth metal-zinc alloys,
magnesium-silver-rare earth metal alloys and magnesium-yttrium-rare
earth metal alloys.
5. A low-friction sliding mechanism according to claim 1, wherein
the diamond-like carbon material of the second sliding member is
hydrogen-free amorphous carbon.
6. A low-friction sliding mechanism according to claim 1, wherein
each of the sliding surfaces of the first and second sliding member
has an arithmetic mean roughness of 0.1 .mu.m or less.
7. A low-friction sliding mechanism according to claim 1, wherein
the first sliding member comprises a base and a coating of the
diamond-like carbon material applied to the base to define the
sliding surface, the coating has a thickness of 0.3 to 2.0 .mu.m
and a micro Vickers hardness HV of 1000 to 3500 as measured by
application of a 10 g load, the second sliding member comprises a
aluminum-based alloy material, and the sliding surface of the
second sliding member has a Brinell hardness H.sub.B of 80 to
130.
8. A low-friction sliding mechanism according to claim 1, wherein
the first sliding member comprises a base and a coating of the
diamond-like carbon material applied to the base to define the
sliding surface, the coating has a thickness of 0.3 to 2.0 .mu.m
and a micro Vickers hardness HV of 1000 to 3500 as measured by
application of a 10 g load, the second sliding member comprises an
magnesium-based alloy material, and the sliding surface of the
second sliding member has a Brinell hardness H.sub.B of 45 to
95.
9. A low-friction sliding mechanism according to claim 1, wherein
each of the first and second sliding members comprises a base and a
coating of the diamond-like carbon material applied to the base to
define the sliding surface, and the coating of each of the first
and second sliding members has a thickness of 0.3 to 2.0 .mu.m and
a micro Vickers hardness HV of 1000 to 3500 as measured by
application of a 10 g load.
10. An internal combustion engine comprising a low-friction sliding
mechanism according to claim 1.
11. A low-friction sliding mechanism according to claim 1, wherein
the fatty-ester friction modifier and the aliphatic-amine friction
modifier comprise C.sub.6-C.sub.30 straight or branched hydrocarbon
chains, respectively, and the lubricant comprises 0.05 to 3.0% by
mass based on the total mass of the lubricant of the at least one
of the fatty-ester friction modifier and the aliphatic-amine
friction modifier.
12. A low-friction sliding mechanism according to claim 1, wherein
the lubricant further comprises polybutenyl succinimide and/or a
derivative thereof.
13. A low-friction sliding mechanism according to claim 12, wherein
the lubricant comprises 0.1 to 15% by mass based on the total mass
of the lubricant of the polybutenyl succinimide and/or the
derivative.
14. A low-friction sliding mechanism according to claim 1, wherein
the lubricant further comprises zinc dithiophosphate in an amount
of 0.1% or less by mass in terms of an phosphorus element based on
a total mass of the lubricant.
15. A low friction sliding mechanism according to claim 1, wherein
at least the sliding surface of the second sliding member comprises
an aluminum-based alloy material, a magnesium-based alloy material
or a diamond-like carbon material.
16. A low-friction sliding mechanism according to claim 1, wherein
at least one of the first and second sliding members comprises a
sliding surface which comprises hydrogen-free amorphous carbon.
17. A low-friction sliding mechanism according to claim 1, wherein
both the first and second sliding members comprise hydrogen-free
amorphous carbon sliding surfaces.
18. A low friction sliding mechanism according to claim 16, wherein
the lubricant comprises an ashless fatty-ester friction
modifier.
19. A low friction sliding mechanism according to claim 16, wherein
the lubricant comprises an ashless aliphatic-amine friction
modifier.
20. A low-friction sliding mechanism, comprising: a first sliding
member having a sliding surface, at least the sliding surface of
the first sliding member comprising a diamond-like carbon material
wherein the diamond-like carbon material of the first sliding
member is hydrogen-free amorphous carbon; a second sliding member
having a sliding surface slidable relative to the sliding surface
of the first sliding member; and a lubricant applied to the sliding
surfaces of the first and second sliding members, the lubricant
comprising friction modifier.
21. A low-friction sliding mechanism, comprising: a first sliding
member having a sliding surface, at least the sliding surface of
the first sliding member comprising a diamond-like carbon material;
a second sliding member having a sliding surface slidable relative
to the sliding surface of the first sliding member; and a lubricant
applied to the sliding surfaces of the first and second sliding
members, the lubricant comprising at least one of an ashless
fatty-ester friction modifier and an ashless aliphatic-amine
friction modifier.
Description
[0001] The present application is a continuation of U.S.
application Ser. No. 11/123,016, filed May 6, 2005, which is a
divisional of U.S. application Ser. No. 10/692,853, filed Oct. 27,
2003, which claims priority from Japanese Patent Application No.
2002-322322 filed on Nov. 6, 2002; Japanese Patent Application No.
2003-207056 filed on Aug. 11, 2003; and Japanese Patent Application
No. 2003-208193 filed on Aug. 21, 2003 the entire contents of which
are incorporated herein by reference.
BACKGROUND OF THE INVENTION
[0002] The present invention relates to a sliding mechanism having
excellent low-friction characteristics, particularly of the kind
for use in an internal combustion engine, a drive train or a hard
disk drive.
[0003] Global environmental problems such as global warming and
ozone layer destruction are coming to the fore. As it is said that
the global warming is significantly effected by CO.sub.2 emission,
the reduction of CO.sub.2 emission, notably the setting of CO.sub.2
emission standards, has become a big concern to each country.
[0004] One of challenges to reduce CO.sub.2 emission is to improve
vehicle fuel efficiency that depends on the performance of engine
sliding members and a lubricant applied thereto. There are the
following approaches to improving vehicle fuel efficiency: (1) to
provide higher abrasion resistance and a lower friction coefficient
for the sliding members, which are generally made of steel
materials in the earlier technology, even under extreme conditions
of abrasion and friction; (2) to lower the viscosity of the
lubricant, thereby reducing viscous resistance in hydrodynamic
lubrication regions and agitation resistance in the engine; and (3)
to mix a suitable friction modifier and other additives into the
lubricant so as to reduce friction losses under the conditions of
mixed lubrication and boundary lubrication.
[0005] In view of the foregoing, many studies have been made on
various friction modifiers including organomolybdenum compounds,
such as molybdenum dithiocarbamate (MoDTC) and molybdenum
dithiophosphate (MoDTP). As a result of the studies, it is found
that the lubricant containing an organomolybdenum compound
successfully produces a friction reducing effect on the steel
sliding members in the early stages of use.
SUMMARY OF THE INVENTION
[0006] Heretofore, the application of hard coating materials to the
engine sliding members has been also examined so that the sliding
members can attain high abrasion resistance and a low friction
coefficient. Above all, a diamond-like carbon (DLC) material is
known for its low-friction performance in the air and therefore
expected to be useful as a coating material for the sliding
members.
[0007] However, the DLC material does not provide a low friction
coefficient in the presence of a lubricant (as disclosed in Japan
Tribology Congress 1999.5, Tokyo, Proceeding Page 11-12, KANO et.
al.). Even when used in combination with the lubricant containing
an organomolybdenum compound, the DLC material cannot provide a
sufficiently low friction coefficient (as disclosed in World
Tribology Congress 2001. 9, Vienna, Proceeding Page 342, KANO et.
al.).
[0008] It is therefore an object of the present invention to
provide a sliding mechanism having stably excellent low-friction
characteristics and high abrasion resistance so as to attain, when
used in an automotive engine, more improvement in vehicle fuel
efficiency than that attained by the earlier technology.
[0009] According to an aspect of the present invention, there is
provided a low-friction sliding mechanism, comprising: a first
sliding member having a sliding surface, at least the sliding
surface of the first sliding member being made of a diamond-like
carbon material; a second sliding member having a sliding surface
slidable relative to the sliding surface of the first sliding
member, at least the sliding surface of the second sliding member
being made of either one of an aluminum-based alloy material, a
magnesium-based alloy material and a diamond-like carbon material;
and a lubricant applied to the sliding surfaces of the first and
second sliding members, the lubricant comprising at least one of an
ashless fatty-ester friction modifier and an ashless
aliphatic-amine friction modifier.
[0010] The other objects and features of the invention will also
become understood from the following description.
BRIEF DESCRIPTION OF THE DRAWINGS
[0011] FIGURE is a schematic illustration of an abrasion test
unit.
DESCRIPTION OF THE EMBODIMENTS
[0012] The present invention will be described below in detail. In
the following description, all percentages (%) are by mass unless
otherwise specified.
[0013] A sliding mechanism according to an exemplary embodiment of
the present invention includes a first sliding member having a
sliding surface, a second sliding member having a sliding surface
slidable relative to the sliding surface of the first sliding
member, and a lubricant applied to the sliding surfaces of the
first and second sliding members.
[0014] The first sliding member has at least its sliding surface
made of a diamond-like carbon (DLC) material, and generally
includes a base made of e.g. an iron-based material, an
aluminum-based alloy material or a resinous material and a coating
of DLC material (hereinafter just referred to as a "DLC coating)
applied to the base so as to define the sliding surface. The first
sliding member may alternatively be formed in one piece of DLC
material. Herein, the DLC material is defined as an amorphous form
of carbon in which carbon exists in both sp.sup.2 and sp.sup.3
hybridizations so as to have a composite structure of graphite and
diamond. Specific examples of the DLC material usable in the
present invention include hydrogen-free amorphous carbon (a-C) that
consists of carbon, hydrogen-containing amorphous carbon (a-C:H)
and metal carbide (MeC) that contains a metal element of titanium
(Ti) or Molybdenum (Mo). For a significant reduction in friction,
hydrogen-free amorphous carbon (a-C) is preferably used.
[0015] The second sliding member has at least its sliding surface
made of either an aluminum-based alloy material, a magnesium-based
alloy material or a DLC material.
[0016] The aluminum-based material for the second sliding member is
preferably a hypoeutectic or hypereutectic aluminum-based alloy
containing 4 to 20% silicon (Si) and 1.0 to 5.0% copper (Cu).
Specific examples of the aluminum-based alloy include AC2A, AC8A,
ADC12 and ADC14 in compliance with JIS H5205.
[0017] The magnesium-based alloy material for the sliding member is
selected for the group consisting of magnesium-aluminum-zinc
(Mg--Al--Zn) alloys, magnesium-aluminum-rare earth metal
(Mg--Al-REM) alloys, magnesium-aluminum-calcium (Mg--Al--Ca)
alloys, magnesium-zinc-aluminum-calcium (Mg--Zn--Al--Ca) alloys,
magnesium-aluminum-calcium-rare earth metal (Mg--Al--Ca-REM)
alloys, magnesium-aluminum-strontium (Mg--Al--Sr) alloys,
magnesium-aluminum-silicon (Mg--Al--Si) alloys, magnesium-rare
earth metal-zinc (Mg-REM-Zn) alloys, magnesium-silver-rare earth
metal (Mg--Ag-REM) alloys, magnesium-yttrium-rare earth metal
(Mg--Y-REM) alloys and combinations thereof. Specific examples of
the magnesium-based alloy include AZ91, AE42, AX51, AXJ, ZAX85,
AXE522, AJ52, AS21, QE22 and WE43 in compliance with ASTM.
[0018] The DLC material usable for the second sliding member can be
exemplified by hydrogen-free amorphous carbon (a-C) that consists
of carbon, hydrogen-containing amorphous carbon (a-C:H) and metal
carbide (MeC) that contains a metal element of titanium (Ti) or
molybdenum (Mo), as in the case with the DLC material usable for
the first sliding member. Among these DLC materials, hydrogen-free
amorphous carbon (a-C) is preferably used. In a case where at least
the sliding surface of the second sliding member is of DLC
material, the second sliding member generally has a base made of
e.g. an iron-based material, an aluminum-based alloy material or a
resinous material and a coating of DLC material (hereinafter
referred to as a "DLC coating") applied to the base so as to define
the sliding surface. Alternatively, the second sliding member may
be formed in one piece of DLC material. Further, it is preferable
that at least one of the DLC materials of the first and second
sliding members is hydrogen-free amorphous carbon (a-C).
[0019] Each of the sliding surfaces of the first and second sliding
members preferably has an arithmetic mean roughness Ra of 0.1 .mu.m
or lower so as to attain a stable sliding between the first and
second sliding members. When the surface roughness Ra exceeds 0.1
.mu.m, the sliding surfaces of the first and second sliding members
are locally subjected to scuffing to cause a great deterioration in
friction coefficient.
[0020] Further, the DLC coating of the first sliding member
preferably has a thickness of 0.3 to 2.0 .mu.m and a micro Vickers
hardness H.sub.V of 1000 to 3500 as measured by the application of
a 10 g load. When the thickness is less than 0.3 .mu.m and the
micro Vickers hardness H.sub.V is less than 1000, the DLC coating
is prone to wear. On the other hand, the DLC coating tends to be
separated from the base when the thickness exceeds 2.0 .mu.m and
the micro Vickers hardness exceeds 3500.
[0021] The sliding surface of the second sliding member, when the
second sliding member is made of the above aluminum-based alloy
material, preferably has a Brinell hardness H.sub.B of 80 to 130.
If the Brinell hardness H.sub.B is less than 80, the sliding
surface of the second sliding surface is prone to wear.
[0022] The sliding surface of the second sliding member, when the
second sliding member is made of the above magnesium-based alloy
material, preferably has a Brinell hardness H.sub.B of 45 to 95. If
the Brinell hardness H.sub.B is less than 45, the sliding surface
of the second sliding surface is also prone to wear.
[0023] When the sliding surface of the second sliding member is
made of the above DLC material, the DLC coating of the second
sliding member preferably has a thickness of 0.3 to 2.0 .mu.m and a
micro Vickers hardness H.sub.V of 1000 to 3500 as measured by the
application of a 10 g load. When the thickness is less than 0.3
.mu.m and the micro Vickers hardness H.sub.V is less than 1000, the
DLC coating is prone to wear. On the other hand, the DLC coating
tends to be separated from the base when the thickness exceeds 2.0
.mu.m and the micro Vickers hardness exceeds 3500.
[0024] The lubricant includes a base oil and at least one of an
ashless fatty-ester friction modifier and an ashless
aliphatic-amine friction modifier.
[0025] The base oil is not particularly limited and can be any base
oil compound or compounds commonly used for a lubricant, such as a
mineral oil or a synthetic oil.
[0026] Specific examples of the mineral oil include oil compounds
prepared by extracting a lubricant fraction from petroleum by
atmospheric or reduced-pressure distillation, and then, purifying
the obtained lubricant fraction by at least one of the following
treatments: solvent deasphalting, solvent extraction,
hydrocracking, solvent dewaxing, hydrotreating and wax
isomerization. In the present invention, the mineral oil prepared
through hydrocracking, hydrotreating and/or wax isomerization is
preferably used.
[0027] Specific examples of the synthetic oil include:
alkylbenzenes, alkylnaphthalenes, polybutenes and hydrides thereof;
poly-.alpha.-olefins, such as 1-octene oligomer and 1-decene
oligomer, and hydrides thereof; diesters, such as ditridecyl
glutarate, dioctyl adipate, diisodecyl adipate, ditridecyl adipate
and dioctyl sebacate; polyol esters, such as trimethylolpropane
caprylate, trimethylolpropane pelargonate, pentaerythritol-2-ethyl
hexanoate and pentaerythritol pelargonate; and mixtures thereof.
Among these synthetic oil compounds, preferred are
poly-.alpha.-olefins, such as 1-octene oligomer and 1-decene
oligomer and hydrides thereof.
[0028] The above-mentioned mineral and synthetic oil compounds may
be used alone, or in the form of a mixture of any two or more
thereof with no limitation on the mixture ratio.
[0029] The aromatic content of the base oil is not particularly
restricted. Herein, the aromatic content is defined as the amount
of aromatics fractions determined according to ASTM D2549 "Standard
Test Method for Separation of Representative Aromatics and
Nonaromatics Fractions of High-Boiling Oils by Elution
Chromatography". The aromatics fractions generally include
alkylbenzenes, alkylnaphthalenes, anthracene, phenanthrene and
alkylates thereof, condensed-ring compounds having four or more
benzeoid rings fused together, and heteroaromatic compounds such as
pyridines, quinolines, phenols and naphthols. In the present
invention, the aromatic content of the base oil is preferably 15%
or less, more preferably 10% or less, and most preferably 8% or
less. When the aromatic content exceeds 15%, the base oil
undesirably deteriorates in oxidation stability. It is noted that
the lubricant may be able to produce a high friction reducing
effect, even if the aromatic content of the base oil is 2% or less
(inclusive of 0%). In such a case, however, there arise a
possibility that the lubricant deteriorates in storage stability,
e.g., when the fatty-ester friction modifier and/or aliphatic-amine
friction modifier is contained in an amount of more than 1%. The
aromatic content of the base oil is thus preferably controlled to
e.g. 2% or more by adding solvent refining mineral oil,
alkylbenzene or the like as needed.
[0030] The kinematic viscosity of the base oil is not particularly
restricted. When the lubricant is used for an internal combustion
engine, the kinematic viscosity of the base oil is preferably 2
mm.sup.2/s or higher, more preferably 3 mm.sup.2/s and, at the same
time, is preferably 20 mm.sup.2/s or lower, more preferably 10
mm.sup.2/s or lower, most preferably 8 mm.sup.2/s or lower, as
measured at 100.degree. C. When the kinematic viscosity is 2
mm.sup.2/s or higher at 100.degree. C., the lubricant is able to
form a sufficient lubricant film so as to attain a high lubricity
and is able to minimize its boil-off under high-pressure
conditions. When the kinematic viscosity is 20 mm.sup.2/s or lower
at 100.degree. C., the lubricant is able to decrease its fluid
resistance and minimize friction resistance in lubrication
regions.
[0031] The viscosity index of the base oil is not particularly
restricted, and is preferably 80 or higher, more preferably 100 or
higher, most preferably 120 or higher, when the lubricant is used
for an internal combustion engine. When the base oil has a higher
viscosity index, the lubricant can attain excellent low-temperature
viscosity properties and produce a good friction reducing
effect.
[0032] The fatty-ester friction modifier and the aliphatic-amine
friction modifier are an fatty acid ester and an aliphatic amine
each having C.sub.6-C.sub.30 straight or branched hydrocarbon
chains, preferably C.sub.8-C.sub.24 straight or branched
hydrocarbon chains, more preferably C.sub.10-C.sub.20 straight or
branched hydrocarbon chains. When the carbon number of the
hydrocarbon chain is not within the range of 6 to 30, there arises
a possibility that the lubricant may not produce a sufficient
friction reducing effect as expected.
[0033] Specific examples of the C.sub.6-C.sub.30 straight or
branched hydrocarbon chain include: alkyl groups, such as hexyl,
heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl,
tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl,
nonadecyl, icosyl, heneicosyl, docosyl, tricosyl, tetracosyl,
pentacosyl, hexacosyl, heptacosyl, octacosyl, nonacosyl and
triacontyl; and alkenyl groups, such as hexenyl, heptenyl, octenyl,
nonenyl, decenyl, undecenyl, dodecenyl, tridecenyl, tetradecenyl,
pentadecenyl, hexadecenyl, heptadecenyl, octadecenyl, nonadecenyl,
icosenyl, heneicosenyl, docosenyl, tricosenyl, tetracosenyl,
pentacosenyl, hexacosenyl, heptacosenyl, octacosenyl, nonacosenyl
and triacontenyl. The above alkyl and alkenyl groups include all
possible isomers.
[0034] The fatty acid ester can be exemplified by esters of fatty
acids having the above hydrocarbon groups and monofunctional
aliphatic alcohols or aliphatic polyols. Specific examples of such
fatty acid esters include glycerol monolate, glycerol diolate,
sorbitan monolate and sorbitan diolate.
[0035] The aliphatic amine can be exemplified by aliphatic
monoamines and alkylene oxide adducts thereof, aliphatic
polyamines, imidazoline compounds, and derivatives thereof.
Specific examples of such aliphatic amines include: aliphatic amine
compounds, such as laurylamine, lauryldiethylamine,
lauryldiethanolamine, dodecyldipropanolamine, palmitylamine,
stearylamine, stearyltetraethylenepentamine, oleylamine,
oleylpropylenediamine, oleyldiethanolamine and
N-hydroxyethyloleylimidazolyne; adducts of the above aliphatic
amines (C.sub.6-C.sub.28 alkyl or alkenyl amines) with alkylene
oxides, such as N,N-dipolyoxyalkylene-N-alkylamines; and
acid-modified compounds prepared by reacting the above aliphatic
amines with C.sub.2-C.sub.30 monocarboxylic acids (such as fatty
acids) or C.sub.2-C.sub.30 polycarboxylic acids (such as oxalic
acid, phthalic acid, trimellitic acid and pyromellitic acid) so as
to neutralize or amidate the whole or part of the remaining amino
and/or imino groups. In the present invention,
N,N-dipolyoxyethylene-N-oleylamine is preferably used.
[0036] The amount of the fatty-ester friction modifier and/or the
aliphatic-amine friction modifier added in the lubricant is not
particularly restricted, and is preferably 0.05 to 3.0%, more
preferably 0.1 to 2.0%, and most preferably 0.5 to 1.4%, based on
the total mass of the lubricant. When the amount of the fatty-ester
friction modifier and/or the aliphatic-amine friction modifier is
less than 0.05%, there arises a possibility that the lubricant may
not produce a sufficient friction reducing effect. When the amount
of the fatty-ester friction modifier and/or the aliphatic-amine
friction modifier exceeds 3.0%, the lubricant produce a good
friction reducing effect but undesirably deteriorates in storage
stability and compatibility to cause precipitations.
[0037] Further, the lubricant desirably includes polybutenyl
succinimide and/or a derivative thereof as an ashless dispersant.
Specific examples of the polybutenyl succinimide usable in the
present invention include compounds represented by the following
general formulas (1) and (2).
##STR00001##
In each of the formulas (1) and (2), n represents an integer of 1
to 5, preferably 2 to 4, so as to attain a good detergent effect.
Further, PIB represents a polybutenyl group derived from
polybutene. The polybutene can be prepared by polymerizing
high-purity isobutene or a mixture of 1-butene and isobutene in the
presence of a boron fluoride catalyst or an aluminum chloride
catalyst in such a manner that the polybutene attains a
number-average molecular weight of 900 to 3,500, preferably 1,000
to 2,000. When the number-average molecular weight of the
polybutene is less than 900, there is a possibility of failing to
attain a sufficient detergent effect. When the number-average
molecular weight of the polybutene exceeds 3,500, the polybutene
may undesirably deteriorate in low-temperature fluidity. In the
production of the polybutenyl succinimide, the polybutene may be
used after purified by removing trace amounts of fluorine and
chlorine residues, which result from the above polybutene
production catalyst, by any suitable treatment (such as adsorption
process or washing process). The amount of the fluorine and
chlorine residues is preferably controlled to 50 ppm or less, more
preferably 10 ppm or less, most preferably 1 ppm or less.
[0038] The production method of the polybutenyl succinimide is not
particularly restricted. For example, the polybutenyl succinimide
can be prepared by reacting an chloride of the above-mentioned
polybutene, or the polybutene from which fluorine and chlorine
residues are removed, with maleic anhydride at 100 to 200.degree.
C. to form butenyl succinate, and then, reacting the thus-formed
butenyl succinate with polyamine (such as diethylene triamine,
triethylene tetramine, tetraethylene pentamine or pentaethylene
hexamine).
[0039] The polybutenyl succinimide derivative can be exemplified by
boron- and acid-modified compounds obtained by reacting the
polybutenyl succinimide of the formulas (1) and (2) with boron
compounds or oxygen-containing organic compounds so as to
neutralize or amidate the whole or part of the remaining amino
and/or imide groups. In the present invention, boron-containing
polybutenyl succinimide, especially boron-containing
bis(polybutenyl)succinimide, is preferably used. Herein, the
content ratio of nitrogen to boron (B/N) by mass in the
boron-containing polybutenyl succinimide is usually 0.1 to 3,
preferably 0.2 to 1.
[0040] The above boron compound can be a boric acid, a borate or a
boric acid ester. Specific examples of the boric acid include
orthoboric acid, metaboric acid and paraboric acid. Specific
examples of the borate include: ammonium salts including ammonium
borates, such as ammonium metaborate, ammonium tetraborate,
ammonium pentaborate and ammonium octaborate. Specific examples of
the boric acid ester include: esters of boric acids and
alkylalcohols (preferably C.sub.1-C.sub.6 alkylalcohols), such as
monomethyl borate, dimethyl borate, trimethyl borate, monoethyl
borate, diethyl borate, triethyl borate, monopropyl borate,
dipropyl borate, tripropyl borate, monobutyl borate, dibutyl borate
and tributyl borate.
[0041] The above oxygen-containing organic compound can be
exemplified by: C.sub.1-C.sub.30 monocarboxylic acids, such as
formic acid, acetic acid, glycolic acid, propionic acid, lactic
acid, butyric acid, valeric acid, caproic acid, enanthic acid,
caprylic acid, pelargonic acid, capric acid, undecylic acid, lauric
acid, tridecanoic acid, myristic acid, pentadecanoic acid, palmitic
acid, margaric acid, stearic acid, oleic acid, nonadecanoic acid
and eicosanoic acid; C.sub.2-C.sub.30 polycarboxylic acids, such as
oxalic acid, phthalic acid, trimellitic acid and pyromellitic acid,
and anhydrides and esters thereof; C.sub.2-C.sub.6 alkylene oxides;
and hydroxy(poly)oxyalkylene carbonates.
[0042] The amount of the polybutenyl succinimide and/or the
derivative thereof added in the lubricant is not particularly
restricted, and is preferably 0.1 to 15%, more preferably 1.0 to
12%, based on the total mass of the lubricant. When the amount of
the polybutenyl succineimide and/or the derivative thereof is less
than 0.1%, there arises a possibility of failing to attain a
sufficient detergent effect. It becomes uneconomical when the
amount of the polybutenyl succineimide and/or the derivative
thereof exceeds 15%. In addition, such a large amount of the
polybutenyl succineimide and/or the derivative thereof tends to
cause a deterioration in demulsification ability.
[0043] Furthermore, the lubricant desirably includes zinc
dithiophosphate represented by the following general formula (3) as
an antioxidant and as an anti-wear agent.
##STR00002##
In the general formula (3), R.sup.4, R.sup.5, R.sup.6 and R.sup.7
each represent C.sub.1-C.sub.24 hydrocarbon groups. The
C.sub.1-C.sub.24 hydrocarbon group is preferably a C.sub.1-C.sub.24
straight-chain or branched-chain alkyl group, a C.sub.3-C.sub.24
straight-chain or branched-chain alkenyl group, a C.sub.5-C.sub.13
cycloalkyl or straight-chain or branched-chain alkylcycloalkyl
group, a C.sub.6-C.sub.18 aryl or straight-chain or branched-chain
alkylaryl group, or a C.sub.7-C.sub.19 arylalkyl group. The above
alkyl group or alkenyl group can be primary, secondary or tertiary.
Specific examples of R.sup.4, R.sup.5, R.sup.6 and R.sup.7 include:
alkyl groups, such as methyl, ethyl, propyl, butyl, pentyl, hexyl,
heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl,
tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl,
nonadecyl, icosyl, heneicosyl, docosyl, tricosyl and tetracosyl;
alkenyl groups, such as propenyl, isopropenyl, butenyl, butadienyl,
pentenyl, hexenyl, heptenyl, octenyl, nonenyl, decenyl, undecenyl,
dodecenyl, tridecenyl, tetradecenyl, pentadecenyl, hexadecenyl,
heptadecenyl, octadecenyl (oleyl), nonadecenyl, icosenyl,
heneicosenyl, docosenyl, tricosenyl and tetracosenyl; cycloalkyl
groups, such as cyclopentyl, cyclohexyl and cycloheptyl;
alkylcycloalkyl groups, such as methylcyclopentyl,
dimethylcyclopentyl, ethylcyclopentyl, propylcyclopentyl,
ethylmethylcyclopentyl, trimethylcyclopentyl, diethylcyclopentyl,
ethyldimethylcyclopentyl, propylmethylcyclopentyl,
propylethylcyclopentyl, di-propylcyclopentyl,
propylethylmethylcyclopentyl, methylcyclohexyl, dimethylcyclohexyl,
ethylcyclohexyl, propylcyclohexyl, ethylmethylcyclohexyl,
trimethylcyclohexyl, diethylcyclohexyl, ethyldimethylcyclohexyl,
propylmethylcyclohexyl, propylethylcyclohexyl, di-propylcyclohexyl,
propylethylmethylcyclohexyl, methylcycloheptyl,
dimethylcycloheptyl, ethylcycloheptyl, propylcycloheptyl,
ethylmethylcycloheptyl, trimethylcycloheptyl, diethylcycloheptyl,
ethyldimethylcycloheptyl, propylmethylcycloheptyl,
propylethylcycloheptyl, di-propylcycloheptyl and
propylethylmethylcycloheptyl; aryl groups, such as phenyl and
naphthyl; alkylaryl groups, such as tolyl, xylyl, ethylphenyl,
propylphenyl, ethylmethylphenyl, trimethylphenyl, butylphenyl,
propylmethylphenyl, diethylphenyl, ethyldimethylphenyl,
tetramethylphenyl, pentylphenyl, hexylphenyl, heptylphenyl,
octylphenyl, nonylphenyl, decylphenyl, undecylphenyl and
dodecylphenyl; and arylalkyl groups, such as benzyl, methylbenzyl,
dimethylbenzyl, phenethyl, methylphenethyl and dimethylphenethyl.
The above hydrocarbon groups include all possible isomers.
[0044] Specific examples of the zinc dithiophosphate usable in the
present invention include zinc diisopropyldithiophosphate, zinc
diisobutyldithiophosphate, zinc di-sec-butyldithiophosphate, zinc
di-sec-pentyldithiophosphate, zinc di-n-hexyldithiophosphate, zinc
di-sec-hexyldithiophosphate, zinc di-octyldithiophosphate, zinc
di-2-ethylhexyldithiophosphate, zinc di-n-decyldithiophosphate,
zinc di-n-dodecyldithiophosphate, zinc diisotridecyldithiophosphate
and mixtures thereof.
[0045] The amount of the zinc dithiophosphate added in the
lubricant is not particularly restricted. The zinc dithiophosphate
is preferably contained in an amount of 0.1% or less, more
preferably in an amount of 0.06% or less, most preferably in a
minimum effective amount, in terms of the phosphorus element based
on the total mass of the lubricant in order to produce a higher
friction reducing effect. When the amount of the zinc
dithiophosphate exceeds 0.1%, there arises a possibility of
inhibiting the effect of the ashless fatty-ester friction modifier
and/or the ashless aliphatic-amine friction modifier.
[0046] The zinc dithiophosphate can be prepared by any known
method. For example, the zinc dithiophosphate may be prepared by
reacting alcohols or phenols having the above R.sup.4, R.sup.5,
R.sup.6 and R.sup.7 hydrocarbon groups with phosphorous
pentasulfide to form dithiophosphoric acid, and then, neutralizing
the thus-formed dithiophosphoric acid with zinc oxide. Herein, the
molecular structure of zinc dithiophosphate differs according to
the alcohols or phenols used as a raw material for the zinc
dithiophosphate production.
[0047] The lubricant may further include any other additive or
additives, such as a metallic detergent, an antioxidant, a
viscosity index improver, a friction modifier other than the
above-mentioned fatty-ester friction modifier and/or the
aliphatic-amine friction modifier, an ashless dispersant other than
the above-mentioned polybutenyl succinimide and/or the derivative
thereof, an anti-wear agent or extreme-pressure additive, a rust
inhibitor, a nonionic surfactant, a demulsifier, a metal
deactivator and/or an anti-foaming agent, when used in an internal
combustion engine. These additives may be used alone or in the form
of a mixture of two or more thereof so as to meet the lubricant
performance required.
[0048] The metallic detergent can be any metallic-detergent
compound commonly used for a lubricant. Specific examples of the
metallic detergent usable in the present invention include
sulfonates, phenates and salicylates of alkali metals or
alkali-earth metals; and mixtures of two or more thereof. Examples
of the alkali metals include sodium (Na) and potassium (K), and
examples of the alkali-earth metals include calcium (Ca) and
magnesium (Mg). In the present invention, sodium and calcium
sulfonates, sodium and calcium phenates, and sodium and calcium
salicylates are suitably used. The total base number and amount of
the metallic detergent can be selected in accordance with the
lubricant performance required. The total base number of the
metallic detergent is usually 0 to 500 mgKOH/g, preferably 150 to
400 mgKOH/g, as measured by perchloric acid method according to ISO
3771 "Determination of base number--Perchloric acid potentiometric
titration method". The amount of the metallic detergent is usually
0.1 to 10% based on the total mass of the lubricant.
[0049] The antioxidant can be any antioxidant compound commonly
used for a lubricant. Specific examples of the antioxidant usable
in the present invention include: phenolic antioxidants, such as
4,4'-methylenebis(2,6-di-tert-butylphenol) and
octyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate; amino
antioxidants, such as phenyl-.alpha.-naphthylamine,
alkylphenyl-.alpha.-naphthylamine and alkyldiphenylamine; and
mixtures of two or more thereof. The amount of the antioxidant is
usually 0.01 to 5% based on the total mass of the lubricant.
[0050] The viscosity index improver can be exemplified by:
non-dispersion type viscosity index improvers, such as methacrylic
acids, copolymers of methacrylic acids and hydrides thereof, and
dispersion type viscosity index improvers, such as copolymers of
methacrylates (including nitrogen compounds). There may be also
used, as the viscosity index improver, copolymers of ethylene and
.alpha.-olefins (such as propylene, 1-butene and 1-pentene) and
hydrides thereof, polyisobutylenes and hydrides thereof, a
hydrogenated copolymer of styrene and diene, a copolymer of styrene
and maleic anhydride and polyalkylstyrenes. The molecular weight of
the viscosity index improver needs to be selected in view of shear
stability. For example, the number-average molecular weight of the
viscosity index improver is desirably in a range of 5,000 to
1,000,000, more desirably 100,000 to 800,000, for dispersion or
non-dispersion type polymethacrylates; in a range of 800 to 5,000
for polyisobutylenes and hydrides thereof; and in a range of 800 to
300,000, more desirably 10,000 to 200,000 for
ethylene/.alpha.-olefin copolymers and hydrides thereof. The above
viscosity index improving compounds can be used alone or in the
form of a mixture of two or more thereof. The amount of the
viscosity index improver is preferably 0.1 to 40.0% based on the
total mass of the lubricant.
[0051] The friction modifier other than the above-mentioned
fatty-ester friction modifier and/or the aliphatic-amine friction
modifier can be exemplified by ashless friction modifiers, such as
boric acid esters, higher alcohols and aliphatic ethers, and
metallic friction modifiers, such as molybdenum dithiophosphate,
molybdenum dithiocarbamate and molybdenum disulfide.
[0052] The ashless dispersant other than the above-mentioned
polybutenyl succinimide and/or the derivative thereof can be
exemplified by polybutenylbenzylamines and polybutenylamines each
having polybutenyl groups of number-average molecular weight of 900
to 3,500, polybutenyl succinimides having polybutenyl groups of
number-average molecular weight of less than 900 and derivatives
thereof.
[0053] The anti-friction agent or extreme-pressure additive can be
exemplified by disulfides, sulfurized fats and oils, olefin
sulfides, phosphate esters having one to three C.sub.2-C.sub.20
hydrocarbon groups, thiophosphate esters, phosphite esters,
thiophosphite esters and amine salts of these esters.
[0054] The rust inhibitor can be exemplified by alkylbenzene
sulfonates, dinonylnaphthalene sulfonates, esters of
alkenylsuccinic acids and esters of polyalcohols.
[0055] The nonionic surfactant and the demulsifier can be
exemplified by noionic polyalkylene glycol surfactants, such as
polyoxyethylene alkylethers, polyoxyethylene alkylphenyleters and
polyoxyethylene alkylnaphthyleters.
[0056] The metal deactivator can be exemplified by imidazoline
compounds, pyrimidine derivatives, thiazole and benzotriazole.
[0057] The anti-foaming agent can be exemplified by silicones,
fluorosilicones and fluoroalkylethers.
[0058] Each of the friction modifier other than the fatty-ester
friction modifier and/or the aliphatic-amine friction modifier, the
ashless dispersant other than the polybutenyl succinimide and/or
the derivative thereof, the anti-wear agent or extreme-pressure
additive, the rust inhibitor and the demulsifier is usually
contained in an amount of 0.01 to 5% based on the total mass of the
lubricant, and the metal deactivator is contained in an amount of
0.0005 to 1% based on the total mass of the lubricant.
[0059] With the above-described structure, the sliding mechanism is
capable of attaining excellent low-friction characteristics and
high abrasion resistance to be fit for a variety of uses,
especially useful for an internal combustion engine, a hard disk
drive and a drive train. The sliding mechanism can be also used as
a sliding gear of an industrial machine.
[0060] The present invention will be described in more detail by
reference to the following examples. However, it should be noted
that the following examples are only illustrative and not intended
to limit the invention thereto.
(1) Assembling of Test Units
[0061] In Examples 1 to 27 and Comparative Examples 1 to 12,
abrasion test units were assembled from varying combinations of
pins, discs and lubricants. Each test unit had three pins and one
disc as shown in FIGURE. The pins, discs and lubricants used were
prepared as follows, and the detailed specifications of the test
units are indicated in TABLES 1 to 3.
(1-11) Preparation of Pins
[0062] A high-carbon chromium material "SUJ2" (i.e. an iron-based
material in compliance with JIS G4805) was formed into pin bases by
grinding and subjected to spheroidizing at 780.degree. C., water
quenching at 30.degree. C. and tempering at 150.degree. C. The
heat-treated pin bases were lapped with lapping tapes in such a
manner as to form their respective base surfaces with different
surface roughness (Ra.ltoreq.0.2 .mu.m). Then, coatings were
applied to the surfaces of the pin bases. The coatings were formed
with different thickness by chemical vapor deposition (CVD) or
physical vapor deposition (PVD) using the following coating
material together with graphite targets.
[0063] [Coating Materials] [0064] DLC: a-C (treated by PVD), a-C:H
(treated by CVD) [0065] TiN (treated by PVD) [0066] CrN (treated by
PVD) Finally, the coatings were lapped with lapping tapes in such a
manner as to form their sliding surfaces with different surface
thickness (Ra.ltoreq.0.1 .mu.m). Each of the pins had a diameter of
5 mm and a length of 5 mm.
(1-2) Preparation of Aluminum-Alloy Discs
[0067] Discs of aluminum-based alloys, such as AC2A, AC8A, ADC12
and ADC14, were heat-treated under the following conditions.
[0068] [Heat Treatment] [0069] AC2A: subjected to age hardening at
510.degree. C. for 8 hours, water quenching at 160.degree. C. for 9
hours and air cooling. [0070] AC8A: subjected to age hardening at
200.degree. C. for 4 hours and air cooling. [0071] ADC12, ADC14: no
heat treatment. Then, the aluminum-alloy discs were subjected to
lapping to form their respective sliding surfaces with different
surface roughness.
(1-3) Preparation of Magnesium-Alloy Discs
[0072] Discs of magnesium-based alloys, such as AZ91D, AE42, AS21,
AX51, AJ52, QE22-T6 and WE43-T6, were heat-treated under the
following conditions.
[0073] [Heat Treatment] [0074] QE22-T6: subjected to age hardening
at 525.degree. C. for 4 hours, water quenching at 200.degree. C.
for 8 hours and air cooling. [0075] WE43-T6: subjected to age
hardening at 525.degree. C. for 4 hours, water quenching at
250.degree. C. for 16 hours and air cooling. [0076] AZ91D, AE42,
AS21, AX51, AJ52: no heat treatment. Then, the magnesium-alloy
discs were subjected to lapping to form their respective sliding
surfaces with different surface roughness.
(1-4) Preparation of DLC Discs
[0077] A high-carbon chromium material "SUJ2" (i.e. an iron-based
material in compliance with JIS G4805) was formed into disc bases
by grinding and subjected to spheroidizing at 780.degree. C., water
quenching at 30.degree. C., and tempering at 150.degree. C. The
heat-treated disc bases were lapped in such a manner as to form
their respective base surfaces with different surface roughness.
Then, DLC coatings were applied to the surfaces of the disc bases.
The DLC coatings were formed by chemical vapor deposition (CVD) or
physical vapor deposition (PVD) using the following DLC coating
material together with graphite targets.
[0078] [Coating Materials] [0079] DLC: a-C (treated by PVD), a-C:H
(treated by CVD) The DLC coatings were lapped with lapping tapes in
such a manner as to form their sliding surfaces with different
surface roughness (Ra.ltoreq.0.1 .mu.m).
(1-5) Preparation of Lubricants
[0080] Each of lubricants A to I was prepared by mixing a base oil
with a friction modifier or modifiers, an ashless dispersant, zinc
dialkyldithiophospate, a metallic detergent and other additives.
The compositions and properties of the thus-prepared lubricants A
to I are shown in TABLE 4. In TABLE 4, the amount of each oil
compound is indicated based on the total mass of the base oil, and
the amount of each additive is indicated based on the total mass of
the lubricant.
(2) Abrasion Test
[0081] The test units of Examples 1 to 27 and Comparative Examples
1 to 12 were subjected to abrasion test under the following test
conditions. The test results are shown in TABLES 1 to 3.
[0082] [Test Condition] [0083] Maximum Hertz's pressure: 80 MPa
[0084] Disc rotation speed: 30 rpm [0085] Lubrication method: Oil
bath [0086] Lubricant temperature: 80.degree. C. [0087] Test time:
60 minutes
TABLE-US-00001 [0087] TABLE 1 Pin Coating Disc Surface Surface
Surface Surface Base Thickness roughness hardness roughness
hardness Friction Material Material (.mu.m) (.mu.m) (Hv) Material
(.mu.m) (H.sub.B) Lubricant coefficient Example 1 SUJ2 a-C 1.1 0.03
1850 AC2A 0.05 80 A 0.055 Example 2 SUJ2 a-C 1.5 0.03 1850 AC8A
0.05 120 B 0.057 Example 3 SUJ2 a-C 1.4 0.03 1850 ADC12 0.05 110 C
0.061 Example 4 SUJ2 a-C 0.8 0.03 1850 ADC14 0.05 130 D 0.066
Example 5 SUJ2 a-C:H 0.7 0.02 1250 AC8A 0.04 120 A 0.083 Example 6
SUJ2 a-C 2.0 0.02 1000 AC2A 0.03 80 B 0.060 Example 7 SUJ2 a-C 1.1
0.03 1850 AC8A 0.10 120 E 0.068 Example 8 SUJ2 a-C 0.9 0.10 1850
AC8A 0.05 120 F 0.066 Example 9 SUJ2 a-C 0.3 0.04 3500 ADC14 0.05
130 G 0.070 Comparative SUJ2 none -- 0.03 1850 AC2A 0.10 80 H 0.14
Example 1 Comparative SUJ2 none -- 0.03 1850 AC8A 0.05 120 E 0.12
Example 2 Comparative SUJ2 a-C 1.2 0.03 1850 ADC14 0.05 130 I 0.10
Example 3 Comparative SUJ2 TiN 2.5 0.04 2300 AC2A 0.05 80 E 0.11
Example 4 Comparative SUJ2 CrN 2.6 0.03 1700 AC8A 0.05 120 E 0.11
Example 5
TABLE-US-00002 TABLE 2 Pin Coating Disc Surface Surface Surface
Surface Base Thickness roughness hardness roughness hardness
Friction Material Material (.mu.m) (.mu.m) (Hv) Material (.mu.m)
(H.sub.B) Lubricant coefficient Example 10 SUJ2 a-C 1.2 0.03 1850
AZ91D 0.04 65 A 0.056 Example 11 SUJ2 a-C 1.4 0.04 1850 AE42 0.06
60 B 0.049 Example 12 SUJ2 a-C 1.3 0.04 1850 AS21 0.05 55 C 0.062
Example 13 SUJ2 a-C 0.9 0.03 1850 AS21 0.04 55 D 0.069 Example 14
SUJ2 a-C:H 0.7 0.03 1250 AE42 0.05 60 A 0.086 Example 15 SUJ2 a-C
1.9 0.02 1000 AX51 0.05 57 B 0.058 Example 16 SUJ2 a-C 1.0 0.02
1850 AJ52 0.08 63 E 0.060 Example 17 SUJ2 a-C 0.8 0.09 1850 QE22-T6
0.06 65 F 0.071 Example 18 SUJ2 a-C 0.4 0.03 3500 WE43-T6 0.06 75 G
0.066 Comparative SUJ2 none -- 0.04 750 AZ91D 0.10 65 H 0.13
Example 6 Comparative SUJ2 none -- 0.03 750 AE42 0.04 60 E 0.12
Example 7 Comparative SUJ2 a-C 1.2 0.04 1850 AS21 0.04 55 I 0.096
Example 8 Comparative SUJ2 TiN 2.4 0.04 2300 AZ91D 0.06 65 E 0.11
Example 9 Comparative SUJ2 CrN 2.7 0.03 1700 AE42 0.05 60 E 0.10
Examole 10
TABLE-US-00003 TABLE 3 Pin Disc Coating Coating Surface Surface
Surface Surface Base Thickness roughness hardness Base Thickness
roughness hardness Friction Material Material (.mu.m) (.mu.m) (Hv)
Material Material (.mu.m) (.mu.m) (Hv) Lubricant coefficient
Example 19 SUJ2 a-C 1.1 0.03 1850 SUJ2 a-C 1.1 0.04 1800 A 0.031
Example 20 SUJ2 a-C 1.5 0.03 1850 SUJ2 a-C:H 1.1 0.03 1800 B 0.046
Example 21 SUJ2 a-C:H 1.4 0.03 1250 SUJ2 a-C 1.9 0.05 1550 C 0.045
Example 22 SUJ2 a-C 0.8 0.03 1850 SUJ2 a-C 0.8 0.05 1800 D 0.033
Example 23 SUJ2 a-C:H 1.8 0.02 1250 SUJ2 a-C:H 1.9 0.04 1200 A
0.060 Example 24 SUJ2 a-C 2.0 0.02 1000 SUJ2 a-C 2.0 0.03 1200 B
0.032 Example 25 SUJ2 a-C 1.1 0.03 1850 SUJ2 a-C 1.1 0.10 1800 E
0.037 Example 26 SUJ2 a-C 0.9 0.10 1850 SUJ2 a-C 0.8 0.05 1800 F
0.035 Example 27 SUJ2 a-C 0.3 0.04 3500 SUJ2 a-C 0.3 0.05 2500 G
0.041 Comparative SUJ2 none -- 0.03 750 AC2A none -- 0.10 80 H
0.140 Example 11 Comparative SUJ2 a-C 0.8 0.03 1850 SUJ2 a-C 0.8
0.05 1800 I 0.080 Example 12
TABLE-US-00004 TABLE 4 Lubricant A B C D E F G H I Base oil Mineral
oil .sup.1) mass % 100 100 -- 100 100 100 100 100 100 Synthetic oil
.sup.2) mass % -- -- 100 -- -- -- -- -- -- Additives Fatty-ester
friction modifier .sup.3) mass % 1.0 1.0 1.0 -- 1.0 1.0 0.2 -- --
Aliphatic-amine friction modifier .sup.4) mass % -- -- -- 1.0 -- 03
-- -- -- Organomolybdenum compound .sup.5) mass % -- -- -- -- -- --
-- -- 1.1 Ashless dispersant .sup.6) mass % 5.0 5.0 5.0 5.0 5.0 5.0
5.0 5.0 5.0 ZDTP .sup.7) mass % -- 0.047 0.047 0.047 0.094 0.094
0.047 0.094 0.094 (in terms of phosphorus element) Metallic
detergent mass % 0.15 0.15 0.15 0.15 0.15 0.15 0.15 0.15 0.15 (in
terms of metal element) Calcium sulfonate .sup.8) mass % 0.5 0.5
0.5 0.5 0.5 0.5 0.5 0.5 0.5 Calcium phenate .sup.9) mass % 0.9 0.9
0.9 0.9 0.9 0.9 0.9 0.9 0.9 Others .sup.10) mass % 7.0 7.0 7.0 7.0
7.0 7.0 7.0 7.0 7.0 Properties Kinematic viscosity at 100.degree.
C. mm.sup.2/s 10.3 10.2 10.0 10.2 10.3 10.3 10.3 10.3 10.2 Total
base number mgKOH/g 6.2 6.2 6.2 6.2 6.5 6.5 6.5 6.5 7.5 according
to perchloric acid method Total base number mgKOH/g 4.5 4.5 4.5 4.5
5.2 5.2 5.2 5.2 6.0 according to hydrochloric method [Remarks]
.sup.1) Hydrocracked mineral oil (kinematic viscosity at
100.degree. C.: 5.0 mm.sup.2/s, viscosity index: 120, aromatic
content: 5.5 mass %) .sup.2) 1-Decene oligomer hydride (kinematic
viscosity at 100.degree. C.: 3.9 mm.sup.2/s, viscosity index: 124,
aromatic content: 0.0 mass %) .sup.3) Glycerol monolate .sup.4)
N,N-dipolyoxyethylene-N-oleylamine .sup.5) Molybdenum
dithiocarbamate (molybdenum content: 4.1 mass %) .sup.6)
Polybutenyl succinimide (nitrogen content: 1.2 mass %) .sup.7) Zinc
dialkyldithiophosphate (zinc content: 9.3 mass %, phosphrous
content: 8.5 mass %, alkyl group: secondary butyl or hexyl group)
.sup.8) Calcium sulfonate (total base number: 300 mgKOH/g, calcium
content: 12.0 mass %) .sup.9) Calcium phenate (total base number:
255 mgKOH/g, calcium content: 9.2 mass %) .sup.10) Including
viscosity index improver, antioxidant, rust inhibitor, demulsifier,
nonionic surfactanct, metal deactivator and anti-foaming agent
[0088] As seen in TABLES 1 to 3, the test units of Examples 1 to 27
showed more excellent low-friction characteristics and higher
abrasion resistance than those of Comparative Examples 1 to 12.
[0089] The test units of Examples 1 to 9 were comprised of the
DLC-coated pins, the aluminum-alloy discs and any of the lubricants
A to G containing at least one of the ashless fatty-ester friction
modifier and/or the ashless aliphatic-amine friction modifier,
respectively. In comparison to the test unit of Comparative Example
1, the friction coefficients of the test units of Examples 1 to 9
were reduced by about 40 to 60%. Similarly, the test units of
Examples 10 to 18 were comprised of the DLC-coated pins, the
magnesium-alloy discs and any of the lubricants A to G,
respectively. The friction coefficients of the test units of
Examples 10 to 18 were also reduced by about 40 to 60% in
comparison to the test unit of Comparative Example 6. The test
units of Examples 19 to 27 were comprised of the DLC-coated pins,
the DLC-coated discs and any of the lubricants A to G,
respectively. The friction coefficients of the test units of
Examples 19 to 17 were reduced by about 50 to 70% in comparison to
the test unit of Comparative Example 11. In addition, any
deterioration in surface appearance was not seen in the sliding
members of Examples 1 to 27 even after the abrasion test.
[0090] Furthermore, the friction reducing effect became more
pronounced as the amount of zinc dithiophosphate contained in the
lubricant was decreased.
[0091] Among the DLC coatings, the a-C coating on the sliding
surface was more effective in reducing friction than the a-C:H
coating. In the case of both the discs and the pins being DLC
coated as shown in Examples 19 to 27, the combination of the a-C
coatings on the sliding surfaces was more effective than the
combination of the a-C coating and the a-C:H coating, and the
combination of the a-C coating, and the a-C:H coating was more
effective than the combination of the a-C:H coatings.
[0092] On the other hand, the test unit of Comparative Example 1
was comprised of the pins with no DLC coatings, the aluminum-alloy
disc and the lubricant H containing neither of the ashless
fatty-ester and aliphatic amine friction modifiers. The test unit
of Comparative Example 6 was comprised of the pins with no DLC
coatings, the magnesium-alloy disc and the lubricant H. Further,
the test unit of Comparative Examples 11 was assembled from the
pins with no DLC coatings, the aluminum-alloy disc with no DLC
coating and the lubricant H. The friction coefficients of the test
units of Comparative Examples 1, 6 and 11 exceeded 0.1 to be much
higher than those of Examples 1 to 27. The test units of
Comparative Examples 2 and 7 were structurally similar to that of
Comparative Examples 1 and 6, and had the pins with no DLC
coatings, the SUJ2 discs with no DLC coatings and the lubricant E
containing the ashless fatty-ester friction modifier, respectively.
The friction coefficients of Comparative Examples 2 and 7 were
slightly lower than those of Comparative Examples 1 and 6 but still
exceeded 0.1. It is estimated that, in the test units of
Comparative Examples 1, 2, 6, 7 and 11, reaction films were formed
predominantly of zinc dithiophosphate (ZnDTP) on the sliding
surfaces of the pins and discs to thereby cause increases in the
friction coefficients. The test unit of Comparative Example 3 was
comprised of the pins with the DLC coatings, the aluminum-alloy
disc and the lubricant I. The test unit of Comparative Example 8
was comprised of the pins with the DLC coatings, the
magnesium-alloy disc and the lubricant I. The test unit of
Comparative Example 12 was comprised of the pins with the DLC
coatings, the disc with the DLC coating and the lubricant I. In the
lubricant I, the organomolybdenum compound was added in place of
the ashless fatty-ester and/or aliphatic-amine friction modifier.
The friction coefficients of the test units of Comparative Examples
3, 8 and 12 were thus nearly 0.1. It is thought that molybdenum
disulfide films were not formed from the lubricant I in the test
units of Comparative Examples 3, 8 and 12, thereby failing to
obtain a sufficient friction reducing effect. The test units of
Comparative Examples 4 and 9 had the pins with the TiN coatings,
and the test units of Comparative Examples 5 and 10 had the pins
with the CrN coatings. The friction coefficients of the test units
of Comparative Examples 4, 5, 9 and 10 were slightly lowered by the
use of the lubricant E, but stood at nearly 0.1. There was little
difference between the friction coefficients of the test units
Comparative Examples 4 and 5 and between the friction coefficients
of the test units of Comparative Examples 9 and 10.
[0093] As described above, the sliding mechanism according to one
exemplary embodiment of the present invention can attain
world-class low-friction characteristics and high abrasion
resistance and is therefore industrially useful. When the sliding
mechanism is used in an internal combustion engine, it becomes
possible to reduce friction loss dramatically so as to provide more
improvement in vehicle fuel efficiency than ever before.
[0094] Although the present invention has been described with
reference to a specific embodiment of the invention, the invention
is not limited to the above-described embodiment. Various
modifications and variations of the embodiment described above will
occur to those skilled in the art in light of the above teaching.
The scope of the invention is defined with reference to the
following claims.
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