Open Access Article
Yu Min Kiw
ab,
Pierre Adama,
Philippe Schaeffer
*a,
Benoît Thiébautb,
Chantal Boyerb and
Nicolas Obrechtb
aUniversity of Strasbourg, CNRS, Institut de Chimie de Strasbourg UMR 7177, F-67000 Strasbourg, France. E-mail: p.schaef@unistra.fr
bTotalEnergies Solaize Research Center, BP22-69360 Cedex, France
First published on 16th August 2022
During engine tests, it has been observed that the combined use of molybdenum dithiocarbamates (MoDTC) and methylene-bis(dithiocarbamates) (MBDTC) in formulated engine oils resulted in better fuel efficiency, keeping the friction coefficient stable at low values for a longer period of time as compared to the same oil devoid of MBDTC. Therefore, the interactions between MBDTC and MoDTC have been investigated at the molecular level. The qualitative and quantitative evolution of MoDTC in two engine oils similarly formulated, but with and without MBDTC, were compared during engine tests using a specifically developed high performance liquid chromatography-mass spectrometry (HPLC-MS) analytical method. Parallel to the molecular study, the evolution of the friction coefficients of both lubricants as well as the evolution of the fuel consumption of the engine were determined. The combined use of MoDTC and MBDTC was shown to exhibit better fuel efficiency and to maintain a relatively low friction coefficient for longer periods of time as compared to the oil devoid of MBDTC. It could be determined that the enhanced performances observed were presumably related to an extension of the lifetime of MoDTC in the engine oil containing MBDTC. Since the MoDTC remaining at the end of the engine test in oil containing MBDTC exclusively bear ligands corresponding to the dithiocarbamate moieties of MBDTC, it can be concluded that the prolonged existence of MoDTC was due to the progressive replacement of the degraded dithiocarbamate ligands on MoDTC educts by those released from MBDTC during engine functioning. As a result, the concentrations of MoDTC could be maintained at a useful level for a longer period in the engine oil containing MBDTC, leading to better fuel consumption performances.
Molybdenum-based complexes such as molybdenum dithiocarbamates (MoDTC, Fig. 1) are effective friction modifiers15–18 that have been shown to reduce friction coefficients to relatively low values under boundary lubrication conditions by generating lamellar structures of MoS2 layers at the tribocontact.19–23 Their effectiveness to reduce friction and to improve fuel efficiency has been investigated using either engine tests or bench friction tests in previous studies.21,24,25 However, it has been shown that MoDTC are unstable during oil ageing and undergo thermo-oxidative degradation during engine operation to form undesirable Mo-species such as molybdenum oxides (MoOx) and other highly oxidized compounds.19,26,27 Moreover, the accumulation of oxidized products can also impede the formation of a MoS2 tribofilm at the rubbing surfaces and cause a drop in friction reduction performance of engine oils.28
Nevertheless, it has been observed that the addition of antioxidants improves significantly the fuel efficiency of lubricant oils containing MoDTC.29,30 Other studies suggest that the combined use of MoDTC with phenolic and amine antioxidants exhibits excellent synergism that provides good retention of friction reducing capabilities of engine oils.31 Sulfur-containing peroxide decomposers and radical inhibitor-type antioxidants such as zinc dithiophosphates (ZnDTP; Fig. 1) are also believed to increase the durability of friction reducing properties of MoDTC and to reduce the decomposition rate of MoDTC under thermo-oxidative conditions.28,32 Thus, it clearly appears that the presence of effective antioxidants may contribute to delay the consumption rate of MoDTC caused by thermo-oxidative degradation.
In this context, the present study is dedicated to the investigation of the impact of MBDTC 2 (Fig. 1) as a lubricant additive on the service life of MoDTC in formulated lubricants. For this purpose, comparative engine tests were performed using the same formulated engine oils containing MoDTC without and with the addition of MBDTC (referred to as “oil A” and “oil AMBDTC”, respectively). Oil performances were compared in terms of tribological properties, duration of the friction reducing capacity of the lubricants, evolution of the fuel consumption of engines and evolution of the concentration of MoDTC with time. The qualitative and quantitative evolution of the MoDTC was monitored using a specifically developed high performance liquid chromatography-mass spectrometry (HPLC-MS) analytical method.33
During the engine tests, oil samples were regularly collected over a period of 143 h for tribological tests and for HPLC-MS analyses.
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| Fig. 2 Schematics of the Anton Paar MCR302 with the ball-on-three-flats geometry. Side (left) and top (right) view. | ||
The following parameters were chosen in our experiments: test temperature was 110 °C, normal load 5 N and sliding speed was kept constant throughout 15 min test at 0.01 m s−1. Upper ball was made of AISI 52100 hardened steel (roughness) and flats were made of 100Cr6 hardened steel (60–66 HRC). The surface roughness of the ball was 0.032 μm (Ra1) and 0.35 μm (Ra2) for the flats. The lubrication regime in the three lubricated contact is determined using the lambda ratio λ described in eqn (1) where h corresponds to the average film thickness in the contact. The lambda value calculated for our test conditions was 0.98. Values below the unity are generally representative of a “boundary lubrication regime”35,36 where significant asperities to asperities contacts occur, favouring the reaction of additives and tribofilm formation.
The observation of friction reduction with MoDTC containing oils during tribotests in this study is also indicative of tribofilm formation characteristic of the boundary lubrication regime.
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Two examples of friction curves measured with the selected tribological setup on an engine lubricant containing MoDTC and tested in fresh conditions (blue curve) and aged conditions (red curve) are shown in Fig. 3. The oil was aged using a glassware oxidation test at 170 °C for 72 h with 100 ppm iron catalyst. The blue curve is characteristic of the formation of a low friction tribofilm on the contact surface, whereas the red curve does not show any friction reduction performance, thereby indicating the lack of activation of the MoDTC in the lubricated contact. Similar curves are generated on engine test samples, and only final friction coefficients measured at the end of the 15 min tribotest are reported in this study.
The precision values on the friction coefficient were calculated over a data set of 84 friction tests on the same reference oil. A standard deviation of 1.8 × 10−3 has been calculated on the friction coefficient leading to a ±0.002 confidence interval at 95% on the mean friction coefficient value.
:
1.5 v/v as the mobile phase. The mass spectrometer was equipped with an atmospheric pressure photoionization source (APPI) used in the positive ionisation mode. Conditions for MS analyses were: nebulizer pressure 50 psi, APPI temperature 420 °C, drying temperature 350 °C, drying gas (N2) flow 5 L min−1, capillary voltage −2 kV, corona 4 microamperes, scan range m/z 400–2000. HPLC-MS analyses were performed in triplicate for each sample collected. Each sample was prepared as follows: 20 μL of internal standard (2,3-bis(n-octadecyloxy)propan-1-ol; 1.7 mg mL−1) were added to an aliquot (20 mg) of each sample collected from engine test diluted in 1 mL of solvent (n-heptane/isopropanol: 95
:
5 v/v). The samples were then diluted by 10-fold using the same solvent before analysis by HPLC-MS.
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| Fig. 4 Evolution of friction coefficients for oil A and AMBDTC as a function of ageing time under engine test conditions. | ||
Similar low values of friction coefficients were observed for both oils during the first 40 h of engine test. However, the friction coefficient of oil A increased sharply and reached a value of μ = 0.119 after 68 h of ageing time, implying a huge loss of the ability of oil A to reduce friction. Such a behaviour is likely related, at least partly, to a loss of performance of MoDTC complexes in this oil. On the other hand, oil AMBDTC showed a much lower value of the friction coefficient after 68 h of ageing time (μ = 0.049) and a value of the friction coefficient comparable to that of oil A after 68 h was attained for oil AMBDTC only after 110 h of ageing time (μ = 0.121). These results, showing that the friction reducing capability of oil AMBDTC after 110 h of ageing time is similar to that of oil A after 68 h of ageing time (μ = 0.121 vs. 0.119), indicate that oil AMBDTC possesses a better retention of friction reducing capabilities over longer periods of time as compared to oil A.
Parallelly to the measurement of friction coefficients, the percentages of fuel economy induced by oils A and AMBDTC relative to fuel consumption when a reference lubricant (SAE 20W-30) was used were measured under stage 1 and 3 engine test conditions as described in section 2.2. The percentages of fuel economy for oils A and AMBDTC relative to the reference oil were calculated for various ageing times according to eqn (2).
| % of fuel economy = [(FCtested oil − FCreference oil)/FCreference oil] × 100 | (2) |
Eqn (2): formula used to calculate the percentage of fuel economy induced by the use of oil A or oil AMBDTC relative to the reference oil (SAE 20W-30) during engine test performed following the ASTM D8114 standard method. FC: fuel consumption (in kg).
Fig. 5 depicts the evolution of the percentage of fuel economy for oils A and AMBDTC as a function of ageing time. Fuel consumption using oil AMBDTC was always shown to be lower than that measured with oil A after 54 h of ageing time under both stage 1 and stage 3 engine test conditions (Fig. 5). These results clearly showed that the use of oil AMBDTC led to a better fuel efficiency of the engine.
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| Fig. 6 Chromatograms (HPLC-MS, APPI) showing the distribution of MoDTC in (a) oil A and (b) oil AMBDTC after 0 h, 40 h, 82 h, 143 h of engine test. | ||
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| Fig. 7 Mass spectra (APPI detection, positive ionisation mode) of (a–c) MoDTC substrates 1a–1c and (d–f) newly formed MoDTC complexes 1d–1f. | ||
The HPLC chromatograms of oils A and AMBDTC at T = 0 h showed the presence of MoDTC 1a–1c which appear as three distinct peaks (partly) separated under the chromatographic conditions used (Fig. 6a and b). The mass spectra of the MoDTC substrates 1a–1c are characterized by a diagnostic complex isotopic pattern due to the presence of 2 molybdenum atoms (Fig. 7a–c). Compounds 1a and 1b (resp. 1c) are separated by 140 mass units (resp. 280 mass units) corresponding to 2 × C5H10 (resp. 4 × C5H10) alkyl chains from the DTC ligands (Fig. 6a–c). For both oils, a progressive decrease in concentration of MoDTC 1a–1c was observed with time, these compounds having completely disappeared between 82 and 143 h (Fig. 6a and b). However, in the case of the oil AMBDTC, the formation with time of new derivatives was noted (Fig. 6b). The specific complex isotopic patterns observed on the mass spectra of the newly formed compounds confirmed that 2 Mo atoms are present on their molecular structures (Fig. 7d–f), like in the case of the genuine MoDTC 1a–1c. In addition, the molecular masses of the newly formed compounds (i.e., [M + H]+ 693–700, 804–817 and 943–957; Fig. 7d–f) are separated by 140 mass units between the first and second eluted compounds, and by 112 mass units between the second and third eluted compounds, suggesting that these compounds correspond to a MoDTC series differing respectively by the presence of a “C10H20” and “C8H16” alkyl entity. Sulfurized MoDTC complexes could also be detected on the mass spectra (Fig. 7) as reported in our previous work.37
The formation of the new Mo species from the MoDTC substrates 1a–1c can be explained by the replacement of one or two of their original dithiocarbamate ligands bearing C8 or C13 alkyl chains by dithiocarbamate ligands bearing C4 alkyl chains, the latter obviously originating from MBDTC 2. The concentration of the new MoDTC complexes 1d–1f increased in oil AMBDTC between 0 and 40 h of engine tests, and progressively decreased between 40 and 143 h, but, in contrast to the genuine MoDTC 1a–1c, they were still present after 143 h of engine functioning (Fig. 6b).
As mentioned above, for both oils A and AMBDTC, the relative concentrations of the MoDTC substrates 1a–1c decreased progressively over time during the first 82 h of engine test and MoDTC 1a–1c were completely consumed between 82 and 143 h (Fig. 8).
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| Fig. 8 Evolution of the relative abundance of MoDTC 1a–1c in (a) oil A and (b) oil AMBDTC during engine test. Error bars correspond to triplicate HPLC-MS analyses of each sample. | ||
At the first sight, it appeared that MoDTC 1a–1c were consumed faster in the case of the oil containing MBDTC (oil AMBDTC), with only ca. 9–14% of the initial MoDTC remaining after 82 h vs. ca. 15–18% in the case of oil A. However, in oil AMBDTC, the decrease of the concentrations of the MoDTC substrates 1a–1c was accompanied by the formation of new MoDTC complexes with dithiocarbamate ligands bearing C4 alkyl chains (see above).
Quantification showed a progressive increase of the concentrations of these newly formed MoDTC complexes 1d–1f during the first 40 h of engine test, followed by their degradation between 40 and 143 h (Fig. 9). It is worth noting that MoDTC 1d and 1e bearing one ligand with C4 alkyl chains were already present at the starting point (T = 0 h) of the engine test (Fig. 9a and b), which can be explained by the fact that this oil was homogenized by a pre-heating step at 60 °C for 60 min.
This clearly shows that the ligand exchange reaction between the genuine MoDTC and MBDTC is a rather fast-occurring process. Examination of the behaviour of the different newly formed MoDTC homologues 1d and 1e throughout the engine test experiment showed that MoDTC 1d and 1e bearing only one exchanged ligand presented the same concentration profile, with a sharp increase in concentration during the first 40 h, followed by a progressive decrease during the next 103 h of engine test. This decrease can be explained by two concomitant processes: first, part of the MoDTC 1d and 1e were progressively consumed upon engine functioning and participated to the formation of the MoS2 tribofilm, and second, since these two species of MoDTC 1d and 1e represent intermediates in the formation of MoDTC 1f bearing two exchanged ligands, they were progressively converted into MoDTC 1f with time. The concentration profile of MoDTC 1f, the end product of the ligand exchange reactions, was different in the sense that formation of this compound was only observed after 40 h of reaction, and then its concentration progressively decreased. Contrary to the MoDTC substrates 1a–1c in both oils A and AMBDTC, these three newly-formed MoDTC 1d and 1e complexes could still be detected in oil AMBDTC after 143 h of engine test and were likely still active to form a MoS2 tribofilm (Fig. 10).
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| Fig. 10 Evolution of relative abundance of the total pool of MoDTC in (a) oil A and (b) oil AMBDTC during engine test. | ||
The evolution of the complete pool of MoDTC in the oils A and AMBDTC after engine tests are shown in Fig. 10. The global concentrations of MoDTC in oil A (sum of 1a–1c) decreased over time with half of the initial MoDTC being consumed after 40 h and fully consumed between 82 and 143 h of engine test (Fig. 10a). For the oil AMBDTC, although the global concentrations of MoDTC complexes (sum of 1a–1f) also decreased over time, small amounts of MoDTC were still present after 143 h, the persisting MoDTC species (ca. 3%) being however exclusively present as newly formed MoDTC 1d–1f (Fig. 10b).
Since the only MoDTC species persisting after 143 h of engine tests bear dithiocarbamate ligands with C4 alkyl chains (i.e., MoDTC 1d–1f) in oil AMBDTC (Fig. 11), their presence can be attributed to the continuous formation of new MoDTC complexes that result from ligand transfer reactions from the MBDTC compound 2 to the genuine MoDTC 1a–1c as well as to the partly altered MoDTC due to the thermo-oxidative conditions prevailing during the engine test (Fig. 11).
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