AU2011212763A1

AU2011212763A1 - Lubricating greases containing lignosulfonate, the production thereof, and the use thereof

Info

Publication number: AU2011212763A1
Application number: AU2011212763A
Authority: AU
Inventors: Alexander Liebenau; Thomas Litters
Original assignee: Fuchs Petrolub SE
Current assignee: Fuchs SE
Priority date: 2010-02-02
Filing date: 2011-01-31
Publication date: 2012-09-06
Anticipated expiration: 2031-01-31
Also published as: JP2013518929A; CN102770513A; DE102010006745A1; HRP20160072T1; HUE026690T2; MX2012008960A; KR20120139730A; EP2531587A1; RU2554873C2; BR112012019181A2; JP5856078B2; CA2788157C; PT2531587E; RS54610B1; RU2012136909A; DK2531587T3; EP2531587B1; AU2011212763B2; KR101833854B1; WO2011095155A1

Abstract

The invention relates to lubricating greases that contain calcium lignosulfonate, comprising a base oil, calcium soaps, calcium lignosulfonate having average molecular weights (weight average) of greater than 10000 g/mol, optionally in addition to further alkaline earth lingosulfonates, which can be produced by heating to greater than 120 °C while reacting and while driving out low-boiling components to produce a basic grease and cooling and adding base oil and optionally additives while mixing, to a corresponding method, and to the use of the lubricating greases containing calcium lignosulfonate.

Description

r-1uVV1 wu Lubricating greases containing lignin sulfonate, production and use thereof The invention relates to a process for producing lubricating greases that contain 5 calcium lignin sulfonate, lubricating greases of such kind, and use thereof. Lignin is a complex polymer based on phenylpropane units, which are cross linked to each other with a wide variety of different chemical bonds. Lignin is present in plant cells together with cellulose and hemicellulose. Lignin itself is a 10 cross-linked macromolecule with average molecular weights of for example at least 10,000 g/mol (weight average). There are essentially 3 types of monolignol monomers that can be identified as monomer components of lignin, and they differ in the degree of their methoxyla 15 tion. They are p-coumaryl alcohol, coniferyl alcohol and sinapyl alcohol. These lignols are incorporated in the lignin structure in the form of hydroxyphenyl (H)-, guaiacyl (G)- and syringal (S) units. Naked-seeded plants (gymnosperms) such as pine trees contain mostly G units and low proportions of H units. All lignins contain small amounts of incomplete or modified monolignols. The primary func 20 tion of lignins in plants is to lend them mechanical stability by cross-linking the vegetable polysaccharides. Lignin constitutes about 1/3 of the dry mass of wood, and according to rough estimates 30% of the non-fossil organic carbon mass on Earth. It is the third most abundant organic material after cellulose and chitin, and is thus a very readily available, renewable raw material for industrial 25 products. Lignin sulfonate is obtained as a by-product of paper manufacturing using the sulfite process. In this process, wood that has been reduced to wood chips is heated for about 7 to 15 hours in the presence of calcium hydrogen sulfite liquor 30 and under pressure (for example 5 to 7 bar) and then the ligninsulfonic acid is removed from the lignocellulose in the form of calcium lignin sulfonate in a washing and precipitation process. Liquors of magnesium, sodium or ammoni um sulfide can also be used instead of calcium hydrogen sulfite, and these pro duce the corresponding magnesium, sodium and ammonium salts of ligninsul 35 fonic acid.

When the washing liquor is evaporated, powdery lignin sulfonates remain. An nual worldwide production of lignin sulfonates is in the order of 55 million tons. Sodium, calcium and magnesium lignin sulfonates are often used as the raw 5 material for plasticising and liquefying concrete and mortar. Lignin sulfonates are also used as pelletising promoters in the kraft animal feed industry and as dispersing or complexing agents in other fields. In modern lubricating grease formulations, a not inconsiderable proportion of 10 the formulation cost is devoted to tribochemically acting extreme pressure and anti-wear additives (EP/AW additive), with the result that they often become the price drivers for lubricating greases. Many of these additives are produced in complicated, multistage synthesis pro 15 cesses, and their use is limited both in terms of the nature of the application and of their effective concentration in the final formulation due to the toxicological side effects that occur in many cases. In some applications, for example in con stant velocity joint shafts or in slow running and heavily loaded rolling bearings, deficient lubrication conditions and/or contact between friction partners is una 20 voidable even when liquid additives are introduced. Former practice in such cases was to use solid lubricants based on inorganic compounds (for example phosphate salts of calcium and zinc), plastic powders (for example PTFE) or metal sulfides (for example MoS 2 ). But these components are also often expen sive and can have a critical effect on the overall cost of a lubricant formulation. 25 Former practice in lubricating grease production was to introduce these addi tives in a second process step, performed after the actual chemical reaction process of thickener formation. In this method, additives, particularly solid lubri cants, must be distributed homogeneously throughout the relatively viscous lu 30 bricating grease by intensive mixing and shearing processes with relatively high mechanical effort in order to obtain their optimum effect. From a modern per spective, the following has often proven disadvantageous and prompted the present invention.

Usual lubricant additives and solid lubricants are normally based on non renewable raw materials and are often poorly biodegradable. Furthermore, most common anti-wear additives and friction reducing lubricant additives entail expensive chemical synthesis processes, which represent a 5 significant cost factor. Particularly when solid lubricants are used for heavily loaded friction points, materials most frequently used are relatively expensive, for example MoS 2 or PTFE. Object / advantage of the invention 10 The object of the invention is therefore to avoid the drawbacks of the prior art as described in the preceding, and to make lignin sulfonates available in lubricating greases both as cost-effective structure forming agents and as additives to promote wear resistance, reduce friction and protect against ageing, and at the 15 same time to lend the lubricating greases good water resistance. The presence of lignin sulfonate means that the use of other common lubricant additives and solid lubricants, particularly MoS 2 , may be minimised or entirely dispensed with. 20 Summary of the invention The invention is defined by the independent claims. Preferred variations repre sent the objects of the dependent claims or are described in the following. 25 According to the process on which the present invention is based, first a precur sor stage (base grease) is prepared by mixing at least - Base oil - Fatty acids and/or esters or salts thereof, wherein the fatty acid salt is at 30 least partly a calcium salt, for producing soaps and containing at least calcium soaps, - Organic and/or inorganic complexing agents if necessary, - Alkaline earth hydroxides, wherein the alkaline earth hydroxides include at least CaOH, 35 - Water if necessary (for example as part of the hydroxides), and - Ca-lignin sulfonate having average molecular weights (weight average) greater than 10000 g/mol. and heating to drive out components with low boiling point when esters are used, and to initiate at least one conversion of the alkaline earth hydroxide with 5 the fatty acids and/or esters thereof and the lignin sulfonate, including reacting with the complexing agents if complexing agents capable of reacting with the alkaline earth hydroxides are used, to form a thickener structure in the base oil. Components with low boiling point are those components that boil at tempera 10 tures up to about 100 C under normal pressure, such as water or C1- to C4 alcohols. In order to produce the base grease, the mixture is preferably heated to tem peratures above 120 0C, or preferably above 180 *C. The conversion to base 15 grease takes place in a heated reactor, which may also be constructed as an autoclave or vacuum reactor. Then, in a second step the formation of the thickener structure is completed by cooling and any additional components such as additives and/or base oil are 20 added to adjust to the desired consistency or the desired properties profile. The second step may be carried out in the same reactor as was used for the first step, but it is preferable if the base grease is transferred from the reactor to a separate stirred tank reactor for cooling and for mixing in the additional compo nents, if any. 25 If necessary, the lubricating grease obtained in this way may be homogenised, filtered and/or deaerated. Preferred substances are Ca/Li-, Li/Ca- and calcium-thickened normal and 30 complex soap greases to which calcium lignin sulfonate has already been add ed before the reaction phase to produce the base grease and is incorporated into the lubricating grease structure via a thermal process in such manner that it is present in highly homogeneous, oil-insoluble form and results in high drop ping point temperatures. 35 The use of alkaline earth salts, preferably calcium salts, for both the fatty acid salts and for the lignin sulfonate guarantees that salt metathesis does not take place either during the production of the base grease or during the application. 5 Salt metathesis, particularly with the salts of sodium, must be prevented in order to obtain a lubricating grease containing lignin sulfonate with good water re sistance and at the same time a high dropping temperature. For this reason, the use of sodium lignin sulfonate and sodium hydroxide must be avoided. Water resistance is understood to mean that the grease is not emulsified by water and 10 conforms to rating level 1-90 (test at 90 0 C) in the test in accordance with DIN 51807-1 (version: 1979-04). Water resistance is further understood to mean that the grease conforms to rating level 1-80 (test at 80 0 C) in the test in accordance with DIN 51807-2 (version 1990-03). 15 The simultaneous application of an excess of alkali in the form of excess calci um hydroxide and possibly also calcium acetate or other calcium salts as the complexing agents is intended to ensure that even small residual amounts of free sulfonic acid groups are neutralised in the lignin sulfonic acid and they lose their hygroscopic, water emulsifying and corrosion promoting action. A high 20 process temperature, above 120 *C and particularly above 180 *C also ensures that the residual moisture that still remains in the lignin sulfonate is evaporated out of the reaction medium completely and any components of the lignin sul fonate that have not been neutralised are neutralised by the calcium hydroxide. 25 Standard lubricating oils that are liquid at room temperature are suitable for use as base oils. The base oil preferably has a kinematic viscosity from 20 to 2500 mm 2 /s, particularly from 40 to 500 mm 2 /s at 40 0 C. The base oils may be classified as mineral oils or synthetic oils. Mineral oils that 30 are eligible for consideration include for example naphthene basic and kerosene basic mineral oils according to their classification in API Group 1. Chemically modified low-aromatic and low-sulfur mineral oils with a small fraction of satu rated compounds and better viscosity/temperature behaviour than Group I oils, classified as API Group 11 and Ill are also suitable. 35 V Regarding synthetic oils, polyethers, esters, polyalphaolefins, polyglycols and alkyl aromatics and mixtures thereof are noteworthy. The polyether compound may contain free hydroxyl groups, but it may also be wholly etherised or termi nal group esterified and/or it may be produced from a starter compound having 5 one or more hydroxy and/or carboxyl groups (-COOH). Polyphenyl ethers, whether alkylated or not, are also possible as the sole component, or better still as components of a mixture. Esters of an aromatic di-, tri- or tetracarboxylic acid with one or more C2- to C22 alcohols present in mixture, alcohols, esters of adipic acid, sebacic acid, trimethylolpropane, neopentyl glycol, pentaerythritol or 10 dipentaerythritol with aliphatic, branched or linear, saturated or unsaturated C2 to C22 carboxylic acids, C18 dimer acid esters with C2 to C22 alcohols, com plex esters, as single components or in any mixture thereof, are also suitable for use. 15 The soaps produced are either pure calcium soaps or mixtures containing calci um soaps, besides calcium soaps particularly lithium soaps and/or aluminium soaps of one or more saturated or unsaturated monocarboxylic acids having 10 to 32 carbon atoms, substituted or not, particularly having 12 to 22 carbon at oms, particularly preferably corresponding hydroxycarboxylic acids. Suitable 20 carboxylic acids are for example lauric acid, myristic acid, palmitic acid, oleic acid, stearic acid or behenic acid and preferably 12-hydroxystearic acid. Even corresponding low alcohol esters, such as corresponding triglycerides and the methyl-, ethyl-, propyl-, isopropyl- or sec.-butyl esters of acid/hydroxy acid, may be used with saponification instead of the free acid group to achieve better dis 25 persion. The soap is converted into a complex soap by the presence of a complexing agent. The complex soaps according to the invention (presence of a complexing agent) have higher dropping points, for example higher than 200 0C (DIN ISO 30 2176). Appropriate quantities for the addition of the complexing agent are from 0.5 to 20 wt %, particularly 0.5 to 10 wt %. The following complexing agents are advantageous for the purposes of the pre sent invention: 35 (a) alkali salt (preferably lithium salt) except sodium salt, alkaline earth salt (preferably calcium salt) or aluminium salt of a saturated or unsaturated monocarboxylic acid, or also hydroxycarboxylic acids having 2 to 8, par ticularly 2 to 4 carbon atoms, or a dicarboxylic acid having 2 to 16, par 5 ticularly 2 to 12 carbon atoms, each of which may be substituted or un substituted, and/or (b) the alkaline and/or alkaline earth salt of boric acid and or phosphoric ac id, particularly the products of its reaction with LiOH and/or Ca(OH) 2 . 10 Complexing agent (a) is preferably solely a calcium salt, particularly if this is used as calcium acetate to produce the base grease. Acetic acid and propionic acid are particularly suitable for use as monocarboxylic acids. Hydroxybenzoic acids such as parahydroxybenzoic acid, salicylic acids, 2-hydroxy-4 hexylbenzoic acid, metahydroxybenzoic acid, 2,5-dihydroxybenzoic acid (gen 15 tisic acid), 2,6-dihydroxybenzoic acid (gamma-resorcylic acid) or 4-hydroxy-4 methoxybenzoic acid are also suitable. Particularly suitable dicarboxylic acids are adipic acid (C 6

H

10 0 4 ), sebacic acid (C 10

H

18 0 4 ), azelaic acid (C 9

H

16 0 4 ) and/or 3-tert.-butyl-adipic acid (C 1

OH

18 0 4 ). 20 Possible substances for use as the borate (b) would include for example metaborate, diborate, tetraborate or orthoborate, such as monolithium orthobo rate or calcium orthoborate. The phosphates might be selected from alkaline (preferably lithium) and alkaline earth (preferably calcium) dihydrogen phosphate, -hydrogen phosphate, or -pyrophosphate. 25 Optionally, bentonites, such as montmorillonite (in which some or all of the so dium ions may have been substituted with ammonium ions), aluminosilicates, clays, silicic acid (e.g. aerosil), oil-soluble polymers (e.g., polyolefins, poly(meth)acrylates, polyisobutylenes, polybutenes or PS) or also di- and poly 30 ureas may also be used as co-thickeners. The bentonites, aluminosilicates, clays, silicic acid and/or oil-soluble polymers may be added to produce the base grease or introduced as additives later, in the second step. The di- and polyure as may be introduced as additives.

6 The compounds according to the invention may also contain other additives as additional substances. Common additional substances for the purposes of the invention are antioxidants, anti-wear agents, corrosion protection agents, deter gents, dyes, lubrication enhancers, viscosity additives, friction reducers and 5 high-pressure additives. Examples of such would be: - Antioxidants such as amine compounds (e.g. alkylamines or 1-phenyl aminonaphthaline), aromatic amines, e.g. phenyl-naphthyl amines or di 10 phenyl amines, phenol compounds (e.g., 2.6-di-tert-butyl-4 methylphenol), sulfur antioxidants, zinc dithiocarbamate or zinc dithio phosphate; - High-pressure additives such as organic chlorine compounds, sulfur, phosphorus or calcium borate, zinc dithiophosphate, organic bismuth 15 compounds; - Substances designed to improve "oiliness", such as C2- to C6- polyols, fatty acids, fatty acid esters or animal or vegetable oils; - Anticorrosion agents such as petroleum sulfonate, dinonylnaphthalene sulfonate or sorbitan esters; 20 - Metal deactivators such as benzotriazol or sodium nitrite; - Viscosity enhancers, such as polymethacrylate, polyisobutylene, oligo dec-1-ene, and polystyrenes; - Anti-wear additives and friction reducers such as organomolybdenum complexes (OMC), molybdenum-di-alkyl-dithiophosphates, molybdenum 25 d i-alkyl-d ithiocarbamates or molybdenum sulfide-di-alkyl dithiocarba mates, particularly molybdenum-di-n-butyl dithiocarbamate and molyb denum disulfide-di-alkyl dithiocarbamate (Mo 2 OmSn(dialkyl carbamate) 2 where m = 0 to 3 and n = 4 to 1), - Friction reducers such as functional polymers, e.g. oleyl amides, organic 30 polyether- and amide-based compounds, for example alkyl polyethylene glycol tetradecylene glycol ether. In addition, the lubricating grease compounds according to the invention also contain usual additives for protection against corrosion, oxidation and 35 attack by metals, which function as chelating compounds, radical scaven gers, UV converters, reaction layer forming agents and the like.

Solid lubricants may be selected for example from the group of polymer powders such as polyamides, polyimides or PTFE, graphite, metal oxides, boron nitride, metal sulfides such as molybdenum sulfide, tungsten disulfide or sulfide mixtures with tungsten, molybdenum, bismuth, tin and zinc base, in 5 organic salts of alkali and alkaline earth metals, such as calcium carbonate, so dium and calcium phosphates. Solid lubricants may be divided into the following four groups: compounds with a lattice layer structure, such as molybdenum disulfide and tungsten disulfide, graphite, hexagonal boron nitride and cer tain metal halides; oxidic and hydroxidic compounds of the transition and 10 alkaline earth metals and carbonates or phosphates thereof; soft metals and/or plastics. The desired, advantageous lubricating properties may be adjusted with the use of lignin sulfonates with having to use solid lubricants. In many cases, solid lubricants may be omitted entirely, or at least signifi cantly reduced. If solid lubricants are used, graphite is the most favourable. 15 Lignin sulfonate may be chosen from calcium lignin sulfonates have a mo lecular weight (Mw, weight average) greater than 10,000, particularly great er than 12,000 or even greater than 15,000 g/mol, for example from 10,000 up to 65,000 g/mol or 15,000 - 65,000 g/mol and particularly containing 2 to 20 12 wt %, particularly 4 to 10 wt %, sulfur (calculated as elemental sulfur) and/or 5 to 15 wt %, particularly 8 to 15 wt % calcium (calculated Ca). Be sides, calcium lignin sulfonates, other alkaline earth lignin sulfonates may also be used. The average molecular weight (weight average) is deter mined for example by size exclusion chromatography. A suitable method is 25 the SEC-MALLS method as described in the article by G. E. Fredheim, S. M. Braaten and B.E. Christensen, "Comparison of molecular weight and molecular weight distribution of softwood and hardwood lignosulfonates" published in "Journal of Wood Chemistry and Technology", Vol. 23, No. 2, pages 197-215, 2003 and the article "Molecular weight determination of lignosulfonates by size 30 exclusion chromatography and multi-angle laser scattering" by the same au thors, published in the "Journal of Chromatography A", Volume 942, edition 1-2, 4 January 2002, pages 191-199 (mobile phase: Phosphate DMSO-SDS, sta tionary phase: Jordi-Glukose-DVB as described in 2.5). Suitable calcium IVU lignin sulfonates are for example the commercially available products Norlig 11 D and Borrement Ca 120 produced by Borregard Lignotech. The lubricating grease according to the invention is characterized by the follow 5 ing composition: a) 55 to 92 wt %, particularly 70 to 85 wt %, base oil, b) 0 to 40 wt %, particularly 2 to 10 wt %, additives, c) 3 to 40 wt %, particularly 5 to 20 wt %, soaps, and d) 0 to 20 wt % or 0.5 to 20 wt %, particularly 0.5 to 10 wt %, complexing 10 agents, and e) excess Ca(OH) 2 , preferably 0.01 to 2 wt %, f) 0.5 to 50, particularly 2 to 15 wt %, and particularly preferably 3 to 8 wt % lignin sulfonate, particularly calcium lignin sulfonate, relative in each case to the overall composition, wherein the components and 15 their preferred variants have been defined in the preceding. It was found that lignin sulfonates function as structure forming agents for water-resistant lubricating greases that also have properties as a solid lubri cants or anti-wear additives and ageing stabilisers. At the same time, lignin sul 20 fonate was observed to have surprisingly synergistic effects with other solid lub ricants, for example with graphite or calcium carbonate. It was also found that lignin sulfonates serve as multifunctional components for lubricants. Due to the large number of polar groups and aromatic structures 25 they contain, their polymer structure and their low solubility in all types of lubri cating oils, lignin sulfonates are suitable for use not only as a thickener compo nent but also as solid lubricants in lubricating greases and lubricating pastes. Their sulfur content also enhances their EP/AW effect in the lubricating greases and the phenolic structures provide an age-inhibiting effect. 30 It is assumed that due to the large number of polymer and polar aromatic units it contains, the lignin sulfonate structure is predominantly planar.

S1I Accordingly, they are able to be deposited very well in layer structures on metal surfaces under due to the effect of external frictional and shearing forces, be cause the aromatic nuclei of the lignin sulfonate enter into an associative recip rocal action with the metal surface, and metallic friction partners are separated 5 from each other effectively and permanently even under heavy loads and high pressures. If calcium lignin sulfonate is added before the start of the reaction phase during the production of soap thickeners, particularly of calcium complex soaps, not 10 only is the thickening effect of these soaps enhanced with a high dropping point, but the anti-wear protection and lubrication effects of corresponding lubricating grease formulations are also enhanced. Consequently, it is beneficial for the distribution and effect of additives and solid lubricants if they are chemically or mechanically incorporated in the thickener structure as an additional structural 15 element in situ during the reaction phase. According to the prior art, it is necessary in many cases to use specially treated, expensive fatty acids, such as 12-hydroxystearic acid, or special complexing agents such as borates or salts of acetic acid, sebacic acid and azelaic acid to 20 manufacture soap greases with high dropping points, yet these substances have little or no additional effect as anti-wear protection and friction reducing additives. If Ca-lignin sulfonates are included, the use of these other compo nents may be reduced significantly or even dispensed with altogether. The use of Ca-lignin sulfonates further offers the capability to formulate high 25 performance lubricating greases on the basis of renewable raw materials and abandon an additive-orientated chemistry that is detrimental to the environment. If oils consisting of unmodified or easily modified native fatty acid esters are thickened using metal soaps based on animal or vegetable fatty acids, and if 30 lignin sulfonates are used as the only additional thickening agent and at the same time the only additive component, lubricating greases are obtained that have been produced almost exclusively on the basis of renewable raw materi als, the only exception being calcium hydroxide used for the metal soaps. The se greases protect against ageing and wear, and have the effect of raising the 35 seizure load and lowering friction when lignin sulfonates are included as a thickener component.

14 The lubricating greases according to the invention are particularly suitable for use in or for constant velocity joint shafts, rolling bearings and gearboxes. If the base oils used consist of readily biodegradable esters, such as those that 5 contain mostly renewable raw materials, the lubricating greases are also suita ble for total loss lubrication in the environmentally sensitive area (for example in mining or agriculture). In the special case of lubrication for maintenance-free constant velocity joint 10 shafts, the first lubricating grease has been formulated using calcium lignin sul fonate that differs from the prior art in that it assures long operating life and good levels of efficiency entirely without the use of MoS 2 and other organic and inorganic molybdenum compounds. 15 The absence of other additives also serves to lower the friction coefficient, pro tect against seizure load and wear and renders the product highly compatible with the materials used in standard commercial constant velocity joint shaft bel lows, such as chloroprene rubber and thermoplastic polyether esters. Since the sulfur contained in lignin sulfonate is bound by thermally stable sulfonate 20 groups, unlike the bound sulfur in conventional additives it is only released at very high temperatures and/or with very high levels of activation energies, such as do not occur in lubricating grease applications except with tribocontacts un der very high loads. In this way, subsequent vulcanisation or crosslinking of rubber materials by the sulfur released from ageing lubricant is largely prevent 25 ed. If calcium lignin sulfonate is used in a lubricating grease formulation that has been adjusted with excess calcium hydroxide to be overbasic, this prevents free lignin sulfonic acid from having a hydrolytic effect on materials used in the bel 30 lows, such as thermoplastic polyether esters. A special aspect of the present invention is that it may be used to obtain cost optimised lubricating grease formulations for lubricating points that are under heavy load, such as in constant velocity joints in particular, and that are well 35 compatible with bellows containing, for example, thermoplastic polyether esters (TPE) and chloroprenes (CR), while offering a high degree of efficiency, low wear and a long service life.

1.) Examples of production Example A (comparison example): 958 g tallow fatty acid, 958 g beef tallow, 958 g calcium acetate, 27.7 g trisodi 5 um phosphate, 27.7 g calcium borate and 358 g calcium hydroxide were placed in a reactor in 12,000 g of a base oil mixture and 150 ml water was added. This base was heated to 198 0 C in a defined temperature programme while stirring so that the added water and the reaction water evaporated. Additives (see ta ble) were added to the base at certain temperatures during the cooling phase. 10 After the base was adjusted to the desired consistency by adding 3700 g of the base oil mixture, the final product was homogenised in a toothed colloid mill. The grease obtained thereby is suitable for use as constant velocity joint shaft grease, for example. 15 Example B: 460 g tallow fatty acid, 445 g beef tallow, 460 g calcium acetate, 27.7 g trisodi um phosphate, 27.7 g calcium borate and 168 g calcium hydroxide and 920 g calcium lignin sulfonate (Norlig 11 D powder manufactured by Borregard Ligno tech) were placed in a reactor in 14,000 g of a base oil mixture and 150 ml wa 20 ter was added. This base was heated to 208 0 C in a defined temperature pro gramme while stirring so that the added water and the reaction water evapo rated. Additives (see table) were added to the base at certain temperatures dur ing the cooling phase. After the base was adjusted to the desired consistency by adding 3450 g of the base oil mixture, the final product was homogenised in 25 a toothed colloid mill. The grease obtained thereby is suitable for use as con stant velocity joint shaft grease, for example. Example C (comparison example): 800 g 12-hydroxy stearic acid, 288 g sebacic acid, 388 g calcium acetate and 30 157.3g calcium hydroxide were placed in a reactor in 5000 g of a base oil mix ture. 64 g LiOH x H 2 0 was dissolved in 250 ml water and added. This base was heated to 200 0C in a defined temperature programme while stirring so that the added water and the reaction water evaporated. Additives were added to the base at certain temperatures during the cooling phase. 35 After the base was adjusted to the desired consistency by adding 3116 g of the base oil mixture, the final product was homogenised in a toothed colloid mill. The grease obtained thereby is suitable for use as rolling bearing grease, for example. 5 Example D: 600 g 12-hydroxy stearic acid, 216 g sebacic acid, 291 g calcium acetate and 720 g calcium hydroxide and 300 g calcium lignin sulfonate (Norlig 11 D powder manufactured by Borregard Lignotech) were placed in a reactor in 5000 g of a 10 base oil mixture. 48 g LiOH x H 2 0 was dissolved in 250 ml water and added. This base was heated to 200 *C in a defined temperature programme while stir ring so that the added water and the reaction water evaporated. Additives were added to the base at certain temperatures during the cooling phase. After the base was adjusted to the desired consistency by adding 3116 g of the 15 base oil mixture, the final product was homogenised in a toothed colloid mill. The grease obtained thereby is suitable for use as rolling bearing grease, for example. Example E (comparison example): 20 1380 g tallow fatty acid, 1360 g beef tallow, 80 g trisodium phosphate, 80 g cal cium borate, 1400 g calcium acetate and 493 g calcium hydroxide were placed in a reactor in 12,000 g of a base oil mixture and 150 ml water was added. This base was heated to 230 0C in a defined temperature programme while stirring so that the added water and the reaction water evaporated. Additives (see ta 25 ble) were added to the base at certain temperatures during the cooling phase. After the base was adjusted to the desired consistency by adding 3125 g of the base oil mixture, the final product was homogenised in a toothed colloid mill. The grease obtained thereby is suitable for use as rolling bearing grease, for example. 30 Example F: 1260 g tallow fatty acid, 1240 g beef tallow, 80 g trisodium phosphate, 80 g cal cium borate, 1278 g calcium acetate, 493 g calcium hydroxide and 885 g calci um lignin sulfonate (Norlig 11 D Powder manufactured by Borregard Lignotech) 35 were placed in a reactor in 12,000 g of a base oil mixture and 150 ml water was added.

This base was heated to 225 0C in a defined temperature programme while stir ring so that the added water and the reaction water evaporated. Additives were added to the base at certain temperatures during the cooling phase. After the base was adjusted to the desired consistency by adding 3125 g of the base oil 5 mixture, the final product was homogenised in a toothed colloid mill. The grease obtained thereby is suitable for use as rolling bearing grease, for example. Example G (comparison example): 975 g calcium-12 hydroxy stearate, 225 g calcium acetate and 15 g calcium 10 borate were placed in a reactor in 3500 g methyl oleate ester. This base was heated to 200 0C in a defined temperature programme while stirring. Additives were added to the base at certain temperatures during the cooling phase. After the base was adjusted to the desired consistency by adding 180 g methyl oleate ester, the final product was homogenised in a 3-roller mill. The lubricating 15 grease obtained thereby is made on the basis of predominantly renewable raw materials. Example H: 841 g calcium 12-hydroxy stearate, 219.5 g calcium acetate, 15 g calcium bo 20 rate and 418 g calcium lignin sulfonate (Norlig 11 D Powder manufactured by Borregard Lignotech) were placed in a reactor in 1965 g methyl oleate ester. This base was heated to 200 0C in a defined temperature programme while stir ring. Additives were added to the base at certain temperatures during the cool ing phase. After the base was adjusted to the desired consistency by adding 25 1684 g trimethylolpropane trioleate ester, the final product was homogenised in a 3-roller mill. The lubricating grease obtained thereby is made on the basis of predominantly renewable raw materials. Examples I and J: 30 The products of example formulations I and J are similar to the production of example H but with the use of different quantities of calcium-12 hydroxy stea rate, calcium acetate and calcium lignin sulfonate and different compositions of ester base oils. The lubricating greases obtained thereby are made on the basis of predominantly renewable raw materials.

'U Table 1: Joint shaft grease formulations Example A B Reference Invention calcium com Description plex calcium complex with 6% lignin with MoS2 sulfonate 1. Thickener: 1.1 Lignin sulfonate: Calcium lignin sulfonate 0.0 6.1 1.2 Fatty acids/-triglycerides: Mixed fatty acids 4.8 2.9 Mixed triglycerides 4.8 2.8 1.3 Alkali hydroxide: Ca(OH)2 1.8 1.5 1.4 Complexing agent: Ca acetate 4.8 3.0 Ca borate 0.1 0.2 2. Base oils: Mixed basic mineral oil (at v40= 100mm 2 /s) 79.5 80.8 3. Additives: Antioxidant 1 0.6 0.5 Antioxidant 2 0.6 0.5 Corrosion protection 0.5 0.2 Solid lubricant, graphite 0.5 1.0 Solid lubricant, MoS2 1.8 0.0 Total 100 100 4. Characteristics Method Unit 4.1 General physical data Penetration unworked DIN ISO 2137 0.1 mm 263 315 Penetration worked 60 double cy cles DIN ISO 2137 0.1 mm 351 340 Copper corrosion 24h / 100 *C DIN 51811 Evaluation level 1-100 1-100 Dropping point DIN ISO 2176 0 C 240 280 Oil separation 18 h/40 'C DIN 51817 % 0.4 2.1 Oil separation 7 d/40 *C DIN 51817 % 2 8.9 4.2 Water resistance Static water resistance 3 h/90 *C DIN 51807-1 Evaluation level 1-90 1-90 Washout loss at 80 *C DIN 51807-2 Evaluation level 1 1 I / Table 1 (continued): Joint shaft grease formulations Example A B Reference Invention calcium )escription complex calcium complex with 6% lignin sul with MoS2 fonate 1.3 Friction reduction 3RV at 80 0C (40 Hz, 1.5 mm Amplitude, 50ON oad) ASTM D D5707-05 :riction coefficient 0.107 0.097 process steady steady 3RV at 150 0C (40Hz, 1.5 mm Amplitude, 50ON oad) ASTM D D5707-05 :riction coefficient 0.097 0.085 >rocess steady steady 1.4 Anti-wear protection /KA weld load DIN 51350-4 N 3400 3800 N /KA calotte 1000N/1min DIN 51350-5 mm 1.02 0.62 1.5 Compatibility with bellows materials t.6.1 Chloroprene Inepsa 4012 168 h/120 0C Shore A DIN 53505 -2 -1 Volume change DIN 53521 % +3.5 -0.5 Change in tensile strength DIN 53504 % -0.5 -1.2 Change in elongation DIN 53504 % -22.1 -19 .6.2 NBR rubber 3RE NBR 34 7d/100 0C DIN 53538-3 Shore A DIN 53505 -2 -3 Volume change DIN 53521 % +3.4 + 3.1 Change in tensile strength DIN 53504 % -2.9 - 5 Change in elongation DIN 53504 % -7.8 -4.5 .6.3 TPE elastomer lytrel 8332 336h/125 0C Shore D DIN 53505 -3 -2 Volume change DIN 53521 % +13.1 +6.2 Change in tensile strength DIN 53504 % -32.9 + 6.7 Change in elongation DIN 53504 % -27 + 61 \rnitel EB 463 336h/125 0C Shore D DIN 53505 -6 0 Volume change DIN 53521 % +10.7 +10.2 Change in tensile strength DIN 53504 % -15 -19.7 Change in elongation DIN 53504 % -10 + 7.8 .6.4 EPDM rubber /amac Y76HR 336h/125 0C Shore A DIN 53505 +3 +5 Volume change DIN 53521 % +6 +0.3 Change in tensile strength DIN 53504 % -17.4 -1.8 Change in elongation DIN 53504 % -39 - 35 . Service life test on the constant velocity joint shaft service life Overrollings (mill.) 13.6 11.2 Werage steady-state temperature 0C 41.1 38.8 E C: jE a a) 0- 0o -t (D1)-C)(ICJ~ aE E L R 6 L 6 'n L.6 Ci L 6 c 6 C-) x (D a a) 02 a) Oc 10 -' q C4 - I a) w X c a 0, (Ua) E E ( (6 N0 6' C5.. >2 33 0 CC) 0 C,) o E p ) C:at a a) a) I) a) 0 C (D0(0 m 0) (0 0 Q Cy mE cu' ~ 'jr 6 aC) 0)C0 C~C) aC) ((D a) X x C'4 0 LMC 4) C) Ea) : EL a 0 &- 0. .2 =3 'm~a C.) 0 5 " w_ LLm a) a) 0 )m0 F U *0 ca- m a -0 0 a) C a) V: U.) C) C 4: i< E C:! x C:D 0D U (D0 C)C)CP. c- 0, CYO CD I C) (0 L a). ~ EE C14 04 0; ) C CCc~ x oE 0 C C) C;)N '~ E ~ - 04 C14 C): CD- oI E C: 0 - a '4-

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Claims

1. A process for producing lubricating greases containing lignin sulfonates comprising 5 a) the step of mixing at least: - a base oil - a calcium soap, possibly produced in situ, with 10 and more carbon at oms, wherein the calcium soaps are produce in situ, at least calcium hy droxide is added, 10 - Calcium lignin sulfonates having average molecular weights (weight av erage) greater than 10,000 g/mol, heating to above 120 0C to initiate the reaction and drive out components hav ing low boiling point to produce a base grease, and b) the step of cooling and of adding base oil and possibly additives while mixing. 15

2. The process according to claim 1, characterized in that in step a) calcium hydroxide is added in addition to any other alkaline earth hydroxides.

3. The process according to claim 1, characterized in that the lubricating 20 grease is adjusted for alkalinity, particularly by adding an excess quantity of calcium hydroxide.

4. The process according to claim 1, characterized in that heating takes place to temperatures higher than 180 C. 25

5. The process according to claim 1, characterized in that in step a) lithium hydroxide, magnesium hydroxide and/or aluminium hydroxide and/or aluminium alcoholates and/or aluminium oxoalcoholates and/or lithium-, magnesium and/or aluminium soaps of a saturated or unsaturated monocarboxylic acid hav 30 ing 10 to 32 substituted or unsubstituted carbon atoms are also used besides calcium hydroxide.

6. The process according to claim 1, characterized in that lubricating grease contains, independently of each other: 35 - 55 to 92 wt %, particularly 70 to 85 wt % base oil, - O to 40 wt %, particularly 2 to 10 wt % additives, - 3 to 40 wt %, particularly 5 to 20 wt %, soaps, and - 0.5 to 20 wt %, particularly 0.5 to 10 wt %, complexing agents, and - optionally excess Ca(OH) 2 , preferably 0.01 to 2 wt %, - 0.5 to 50, particularly 2 to 15 wt %, and particularly preferably 4 to 8 wt % lignin sulfonate, optionally in addition to other alkaline earth lignin sul 5 fonates, relative in each case to the overall composition of the lubricating grease.

7. The process according to claim 1, characterized in that the base grease of step a) can be produced by using 10 - 40 to 70 wt %, particularly 45 to 60 wt % base oil, - 10 to 60 wt %, particularly 15 to 50 wt %, soaps, and - 0 to 30 wt %, particularly 5 to 20 wt %, complexing agent, and - optionally excess Ca(OH) 2 , preferably 0.02 to 4 wt %, - 0.7 to 50, particularly 4 to 30 wt % calcium lignin sulfonate, optionally in 15 addition to other alkaline earth lignin sulfonates, relative in each case to the composition of the base grease.

8. The process according to claim 1 or 4, characterized in that the base grease contains, independently of each other, 0.2 - 5 wt % graphite and/or no 20 solid lubricant or less than < 1 wt % solid lubricant, particularly no MoS 2 .

9. The process according to claim 1, characterized in that the calcium soap is produced in-situ as a byproduct of reacting calcium hydroxide with a saturat ed or unsaturated monocarboxylic acid having 10 to 32 carbon atoms, particu 25 larly having 16 to 20 carbon atoms, optionally substituted for example by hy droxy, as an ester or anhydride.

10. The process according to claim 1, characterized in that the complexing agent as a product of the reaction of a calcium salt, particularly calcium hydrox 30 ide, with a saturated or unsaturated monocarboxylic acid having 2 to 8, particu larly 2 to 4, carbon atoms, or a dicarboxylic acid having 2 to 16, particularly 2 to 12 carbon atoms, each of which may or may not be substituted for example by hydroxyl as an ester or anhydride, is added during step a).

11. The process according to claim 1, characterized in that the complexing agent is a calcium salt of a carboxylic acid and is produced in situ during step a) by adding a saturated or unsaturated monocarboxylic acid having 2 to 8, partic ularly 2 to 4, carbon atoms or a dicarboxylic acid having 2 to 16, particularly 2 to 5 12 carbon atoms, each of which may or may not be substituted for example by hydroxyl as an ester or anhydride.

12. The process according to at least one of claims 1 to 11, characterized in that the calcium lignin sulfonate is dewatered to values less than 0.5 wt % water 10 before it is added, for example by heating in the base oil to above 95 *C, partic ularly above 100 0 C, for example to 120 0 C.

13. The process according to at least one of claims 1 to 12, characterized in that the composition contains 0.5 to 20 wt %, particularly 0.5 to 10 wt % of the 15 complexing agent.

14. A lubricating grease compound containing - 55 to 92 wt %, particularly 70 to 85 wt %, base oil, - 0 to 40 wt %, particularly 2 to 10 wt %, additives, 20 - 3 to 40 wt % particularly 5 to 20 wt %, calcium soaps having 10 and more carbon atoms, - 0 to 20 wt %, particularly 0.5 to 10 wt %, complexing agent, and - optionally excess Ca(OH) 2 , preferably 0.01 to 2 wt %, - 0.5 to 50, particularly 2 to 15 wt %, and particularly preferably 2 to 8 wt % 25 calcium lignin sulfonate, possibly in addition to other alkaline earth lignin sulfonates, relative in each case to the total composition of the lubricating grease.

15. The composition according to claim 14, characterized in that the compo 30 sition has a cone penetration value (worked penetration) from 265 to 385 mm/10 (at 25 *C), preferably 285 to 355 mm/10, determined according to ISO

2137.

16. The composition according to at least one of claims 14 or 15, characterized in that the base oil has a kinematic viscosity from 20 to 2500 mm 2 /s, preferably from 40 to 500 mm 2 /s, at 40 0C. 5

17. The composition according to at least one of claims 14 to 16, characterized in that the complexing agent consists of: - an alkali salt, preferably lithium salt, alkaline earth salt, preferably calcium salts, or aluminium salt of a saturated or unsaturated monocarboxylic acid having 2 to 8, particularly 2 to 4, carbon atoms or a dicarboxylic acid hav 10 ing 2 to 16, particularly 2 to 12, carbon atoms, each of which may or may not be substituted.

18. The composition according to at least one of claims 14 to 17, character ized in that the additive comprises one or more members selected from the fol 15 lowing group: - Antioxidants such as amine compounds, phenol compounds, sulphur anti oxidants, zinc dithiocarbamate or zinc dithiophosphate; - High pressure additives such as organic chlorine compounds, sulfur, phosphorus or calcium borate, zinc dithiophosphate, organic bismuth 20 compounds; - C2- to C6- polyols, fatty acids, fatty acid esters or animal or vegetable oils; - Anticorrosion agents such as petroleum sulfonate, dinonyInaphthalone sul fonate or sorbitan ester; - Metal neutralisers such as benzotriazol or sodium nitrite; 25 - Viscosity enhancers such as polymethacrylate, polyisobutylene, oligo-dec 1-enes, and polystyrenes; - Anti-wear additives such as molybdenum dialkyl dithiocarbamates or mo lybdenum sulphide dialkyl dithiocarbamates, aromatic amines; - Friction modifiers such as functional polymers, for example oleyl amides, 30 polyether- and amide-based organic compounds, or molybdenum dithio carbamate, and - solid lubricants, for example polymer powders such as polyamides, poly imides or PTFE, graphite, metal oxides, boron nitride, metal sulphides such as molybdenum disulfide, tungsten disulfide or mixed sulphides with tungsten, molybdenum, bismuth, tin and zinc base, inorganic salts of 5 alkaline and alkaline earth metals, such as calcium carbonate, sodium and calcium phosphates.

19. The composition according to at least one of claims 14 to 18, characterized in that the lubricating grease is water-resistant, particularly 10 a) in accordance with the test defined in DIN 51807-1, evaluation level 1-90, and/or b) in accordance with the test defined in DIN 51807-2 evaluation level 1-80.

20. The composition according to at least one of claims 14 to 19, 15 characterized in that the calcium lignin sulfonate has an average molecular weight (Mw, weight average) or more than 10,000, particularly more than 12,000, or even more than 15,000 g/mol, and independently thereof con tains 2 to 12 wt %, particularly 4 to 10 wt %, sulfur (calculated as elemental sulfur) and/or also independently 5 to 15 wt %, particularly 8 to 15 wt % 20 calcium.

21. The composition according to at least one of claims 14 to 20, characterized in that the lubricating grease contains a base oil based on renew able raw materials and/or a fraction of 95% or more thereof is made on the ba 25 sis of renewable raw materials.

22. The composition according to at least one of claims 14 to 21, characterized in that the composition contains a 0.5 to 20 wt %, particularly 0.5 to 10 wt % complexing agent. 30

23. Use of the composition according to at least one of claims 14 to 22 for lubricating at least a constant velocity joint, particularly as part of homokinetic joint shafts, transmissions and a rolling or friction bearing. 35