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    • 专利摘要:
    process to produce lubricating greases, lubricating grease composition, use of a composition. The invention relates to lubricating greases containing calcium lignosulfonate comprising a base oil, calcium soaps, calcium lignosulfonate having average molecular weights (average weight) greater than 10,000 g / mol, optionally in addition to other alkaline earth lignosulfonates. , which can be produced by heating above 130 ° C while reacting and expelling low boiling components to produce basic grease, and cooling and addition of base oil and optionally additives while mixing, to a corresponding method, and to use. of lubricating greases containing calcium lignosulfonates.
    公开号:BR112012019181B1
    申请号:R112012019181
    申请日:2011-01-31
    公开日:2018-09-11
    发明作者:Liebenau Alexander；Litters Thomas
    申请人:Fuchs Petrolub Ag；
    IPC主号:
    专利说明:

    (54) Title: PROCESS TO PRODUCE LUBRICATION Greases, LUBRICATION Grease COMPOSITION, USE OF A COMPOSITION.
    (51) Int.CI .: C10M 135/10; C10M 141/08; C10M 159/24; C10N 40/02; C10N 2/30; C10N 30/06; C10N 30/12; C10N 10/02; C10N 10/04; C10N 50/10 (30) Unionist Priority: 02/02/2010 DE 10 2010 006 745.8 (73) Holder (s): FUCHS PETROLUB AG (72) Inventor (s): THOMAS LITTERS; ALEXANDER LIEBENAU (85) National Phase Start Date: 07/31/2012 “PROCESS TO PRODUCE LUBRICATION Greases, LUBRICATION Grease COMPOSITION, USE OF A COMPOSITION”
    The invention relates to a process for producing lubricating greases containing calcium lignosulfonate, lubricating greases of this kind, and their use.
    Lignin is a complex polymer based on phenylpropane units, which are cross-linked with a wide variety of different chemical bonds. Lignin is present in plant cells along with cellulose and hemicellulose. Lignin itself is a cross-linked macromolecule with average molecular weights of, for example, at least 10,000 g / mol (average weight).
    There are essentially 3 types of monolignol monomers that can be identified as monomeric components of lignin, and they differ in the degree of their methoxylation. They are p-coumaryl alcohol, coniferyl alcohol and synaphyl alcohol. These lignols are incorporated into the lignin structure as hydroxyphenyl (H), guaiac (G) and syringal (S) units. Exposed seedlings (gymnosperms) such as pines, contain mainly G units and low proportions of H units. All lignins contain small amounts of incomplete or modified monolignols. The primary function of lignins in plants is to give them mechanical stability by crosslinking plant polysaccharides. Lignin constitutes about 1/3 of the dry mass of wood, and according to estimates approximately 30% of the mass of non-fossil organic carbon on Earth. It is the third most abundant organic matter after cellulose and chitin, and is thus a renewable raw material that is very readily available for industrial products.
    Lignosulfonate is obtained as a by-product of papermaking using the sulfite process. In this process, the wood that has been reduced to wood chips is heated for about 7 to 15 hours in the presence of a liquid substance of calcium sulfite, hydrogen and under pressure (for example, from 5 to 7 bar) and then lignosulfonic acid is removed from lignocellulose in the form of calcium lignosulfonate in a wash and precipitation process. The liquid substances of magnesium, sodium or ammonium sulfide can also be used in place of calcium hydrogen sulfite, and these produce the corresponding magnesium, sodium and ammonium salts of lignosulfonic acid.
    When the washing liquid substance is evaporated, powdered lignosulfonates remain. The annual world production of lignosulfonates is in the order of 55 million tons.
    Sodium, calcium and magnesium lignosulfonates are often used as the raw material for the plasticization and liquefaction of concrete and mortar. Lignosulfonates are also used as granulation promoters in the kraft animal feed industry and as dispersants or complex agents in other fields.
    In modern lubricating grease formulations, a not insignificant proportion of the formulation cost is dedicated to the extreme pressure of tribochemical action and anti-wear additives (EP / AW additive), with the result that price drivers are often taken for lubricating greases.
    Many of these additives are produced in complicated multistage synthesis processes, and their use is limited both in terms of the nature of the application and its effective concentration in the final formulation due to the toxicological side effects that occur in many cases. In some applications, for example, on constant speed or idling joint shafts and heavily loaded rolling bearings, poor lubrication conditions and / or contact between friction pairs are inevitable, even when liquid additives are introduced . The previous practice in such cases was to use solid lubricants based on inorganic compounds (for example, calcium and zinc phosphate salts), plastic powders (for example PTFE) or metal sulfides (for example M0S2). But these components are also often expensive and can have a critical effect on the total cost of a lubricant formulation.
    The previous practice in the production of lubricating grease was to introduce these additives in a second stage of the process, performed after the actual chemical reaction process of thickener formation. In this method, additives, particularly solid lubricants, must be distributed evenly throughout the relatively viscous lubricating grease through intensive mixing and shearing processes with relatively high mechanical effort, in order to obtain their ideal effect. From a modern perspective, what follows often proved to be disadvantageous and prompted the present invention.
    Lubricating greases containing sodium soaps or lithium soaps and sodium lignin sulfonates are still known from US3239537 A. However, this is not suitable for use in lubricating constant speed joint shafts, mainly because the grease attacks TPE materials that are used in the bellows.
    The usual lubricant additives and solid lubricants are usually based on non-renewable raw materials and are often poorly biodegradable.
    In addition, the most common anti-wear additives and friction-reducing lubricant additives involve expensive chemical synthesis processes, which represent a significant cost factor. Particularly when solid lubricants are used for heavily loaded friction points, the most frequently used materials are
    3a relatively expensive, for example, M0S2 or PTFE.
    Purpose / advantage of the invention
    The aim of the invention is, therefore, to avoid the disadvantages of the prior art as described in the preceding one, and to take the ligninosulfonates available in the lubricating greases both as cost-effective forming agents and as additives to promote resistance following page 4 wear, reduce friction and protect against aging, while providing lubrication greases with good water resistance.
    Does the presence of lignosulfonate mean that the use of other common lubricant additives and solid lubricants, particularly MoS 2 can be minimized or completely suppressed.
    Summary of the Invention
    The invention is defined by the independent claims. Preferred variations represent the objectives of the dependent claims or are described below.
    According to the process on which the present invention is based, first a precursor stage (base grease) is prepared by mixing at least
    - Base Oil
    - Fatty acids and / or esters or their salts, in which the fatty acid salt is at least partially a calcium salt, to produce soaps and containing at least calcium soaps,
    - Organic and / or inorganic complexing agents if necessary,
    - alkaline earth hydroxides, where alkaline earth hydroxides include at least CaOH,
    Water if necessary (for example, as part of hydroxides), and
    Ca-lignin sulfonate having average molecular weights (average weight) greater than 10,000 g / mol.
    and heating to expel components with low boiling point when esters are used, and to initiate at least one conversion of alkaline earth hydroxide with fatty acids and / or their esters and lignosulfonate, including the reaction with complexing agents if complexing agents capable of reacting with alkaline earth hydroxides are used to form a thickener structure in the base oil.
    Low-boiling components are those components that boil at temperatures 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 temperatures above 120 ° C, or preferably above 180 ° C. The conversion of the base grease takes place in a heated reactor, which can also be built as an autoclave or vacuum reactor.
    Then, in a second step the formation of the thickening structure is completed by cooling and any additional components such as additives and / or base oil are added to adjust the desired consistency or the desired profile of the properties. The second step can be performed in the same reactor that was used for the first step, but it is preferable that the grease base is transferred from the reactor to a separate stirred tank reactor for cooling and mixing in the additional components, if any.
    If necessary, the grease obtained in this way can be homogenized, filtered and / or deoxygenated.
    Preferred substances are Ca / Li-, Li / Ca- and normal and complex soap greases thickened with calcium to which calcium lignosulfonate has already been added before the reaction phase to produce the base grease and is incorporated into the grease structure of lubrication through a thermal process in such a way that it is present in the highly homogeneous oil insoluble form and results in high drop point temperatures.
    The use of alkaline earth salts, preferably calcium salts, for both fatty acid and lignosulfonate salts, ensures that salt metathesis does not occur during the production of the base grease or during application.
    Salt metathesis, particularly with sodium salts, should be avoided in order to obtain a lubricating grease containing lignosulfonate with good water resistance and at the same time a high drop temperature. For this reason, the use of sodium lignosulfonate and sodium hydroxide should be avoided. Water resistance is understood to mean that the grease is not emulsified by water and is in accordance with an assessment level of 1 to 90 (test at 90 ° C) in the test according to DIN 51807-1 (version: 1979-04 ). It is also understood that the water resistance means that the grease complies with the evaluation level from 1 to 80 (test at 80 ° C) in the test according to DIN 51807-2 (version 1990-03).
    The simultaneous application of an excess of alkali in the form of excess calcium 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 neutralized in the lignosulfonic acid and lose their hygroscopic water emulsification and corrosion-promoting action. An elevated process temperature, above 120 ° C and in particular above 180 ° C, also ensures that the residual moisture that still remains in the lignosulfonate is evaporated out of the reaction medium completely and any components of the lignosulfonate that have not been neutralized are neutralized by calcium hydroxide.
    Standard lubricating oils that are liquid at room temperature are suitable for use as base oils. The base oil preferably has a kinematic viscosity of 20 to 2500 mm / s, particularly 40 to 500 mm 2 / s at 40 ° C.
    Base oils can be classified as mineral oils or synthetic oils. Mineral oils that are eligible for consideration include, for example, mineral oils of basic naphthene and basic kerosene according to their classification in API Group I. Mineral oils with low aromatic and low sulfur content chemically modified with a small fraction of saturated compounds and better viscosity / temperature behavior than Group I oils, classified as API Groups II and III, are also suitable.
    With regard to synthetic oils, polyethers, esters, polyalphaolefins, polyglycols and aromatics of alkyl and their mixtures are noteworthy. The polyether compound can contain free hydroxyl groups, but it can also be fully ethered or subjected to ester at the terminal group and / or it can be produced from a starting compound having one or more hydroxy and / or carboxyl groups (-COOH). Polyphenyl ethers, whether alkylated or not, are also possible as the sole component, or better yet as components of a mixture. Esters of an aromatic di-, tri- or tetracarboxylic acid with one or more C2 to C22 alcohols present in the mixture, alcohols, adipic acid esters, sebacic acid, trimethylolpropane, neopentyl glycol, pentaerythritol or dipentaerythritol with C2-C22 aliphatic carboxylic acids , branched or linear, saturated or unsaturated, esters of dimeric acid Cl8 with C 2 to C22 alcohols complex esters, as isolated components or in any mixture thereof, are also suitable for use.
    The soaps produced are pure calcium soaps or mixtures containing calcium soaps, in addition to calcium soaps particularly lithium soaps and / or aluminum soaps of one or more saturated or unsaturated monocarboxylic acids having 10 to 32 carbon atoms, substituted or no, in particular having from 12 to 22 carbon atoms, the corresponding hydroxycarboxylic acids are particularly preferable. Suitable carboxylic acids are, for example, lauric acid, myristic acid, palmitic acid, oleic acid, stearic acid or behenic acid and preferably 12-hydroxystearic acid. Even the corresponding lower alcohol esters, such as the corresponding triglycerides and the acid / hydroxy acid methyl-, ethyl-, propyl-, isopropyl- or sec.-butyl esters, can be used with saponification instead of the free acid group to achieve better dispersion.
    The soap is converted into a complex soap by the presence of a complexing agent. Complex soaps containing lubricating grease compositions according to the invention (presence of a complexing agent) have higher drop points, for example, higher than 200 ° C (DIN ISO 2176). Suitable amounts for the addition of the complexing agent are from 0.5 to 20% by weight, particularly from 0.5 to 10% by weight.
    The following complexing agents are advantageous for the purposes of the present invention:
    (a) alkaline salt (preferably lithium salt), except sodium salt, alkaline earth salt (preferably calcium salt) or aluminum salt of a saturated or unsaturated monocarboxylic acid, or also hydroxycarboxylic acids having from 2 to 8, particularly from 2 to 4 carbon atoms, or a dicarboxylic acid having from 2 to 16, particularly from 2 to 12 carbon atoms, each of which can be substituted or unsubstituted, and / or (b) the alkaline salt and / or alkaline earth acid of boric acid and / or phosphoric acid, in particular the products of its reaction with LiOH and / or Ca (OH) 2 .
    The complexing agent (a) is preferably only a calcium salt, particularly if it 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 (gentisic acid), 2,6-dihydroxybenzoic acid (gamma-resorclic acid ) or 4-hydroxy-4-methoxybenzoic acid are also suitable. Particularly suitable dicarboxylic acids are adipic acid (C 6 H2 0 ) ; sebacic acid (Ci 0 Hi 8 O 4 ), azelaic acid (C9H16O4) and / or 3-tert-butyl-adipic acid (C 10 H 3 8 O 4 ).
    Possible substances for use such as borate (b) should include, for example, metaborate, diborate, tetraborate or orthborate, such as monolithium orthborate or calcium orthborate. Phosphates can be selected from dihydrogen phosphate, hydrogen phosphate or alkaline pyrophosphate (preferably lithium) and alkaline earth (preferably calcium).
    Optionally, bentonites, such as montmorillonite (where some or all of the sodium ions may have been replaced with ammonium ions), aluminosilicates, clays, silicic acid (for example, aerosil), oil-soluble polymers (for example, polyolefins , poly (meth) acrylates, polyisobutylene, polybutene or PS) or also di- and polyurea can also be used as co-thickeners. Bentonites, aluminum silicates, clays, silicic acid and / or oil-soluble polymers can be added to produce the base grease or introduced as additives later, in the second step. Di- and poly-ureas can be introduced as additives.
    The compounds according to the invention can also contain other additives as additional substances. Additional substances common for the purposes of the present invention are antioxidants, anti-wear agents, corrosion protection agents, detergents, dyes, lubrication enhancers, viscosity additives, friction reducers and high pressure additives.
    Examples of these would be:
    - Antioxidants such as amine compounds (for example, alkylamines or 1-phenyl-aminonaphthaline), aromatic amines, for example, phenyl-naphthyl amines or di-phenyl amines, phenol compounds (for example, 2,6-di -tert-butyl-4-methylphenol), sulfur antioxidants, zinc dithiocarbamate or zinc dithiophosphate;
    High pressure additives such as organic chlorine compounds, sulfur borate, phosphorus or calcium, zinc dithiophosphate, organic bismuth compounds;
    Substances designed to improve “greasiness”, such as C2 to C6 polyols, fatty acids, fatty acid esters or animal or vegetable oils;
    Anti-corrosion agents such as petroleum sulfonate, dinonylnaphthalene sulfonate or sorbitan esters;
    Metal deactivators such as benzotriazole or sodium nitrite;
    Viscosity enhancers, such as polymethacrylate, polyisobutylene, oligodec-1-ene, and polystyrenes;
    - Anti-wear and friction-reducing additives such as organomolibdenum (OMC) complexes, molybdenum-di-alkyl-dithiophosphates, molybdenum-di-alkyl-dithiocarbamates or molybdenum sulfide-di-alkyl-dithiocarbamates, particularly molybdenum-di-n-butyl dithiocarbamate and molybdenum disulfide-di-alkyl dithiocarbamate (Mo 2 O m S n (dialkyl carbamate) 2 where m = 0a3en = 4al),
    - Friction reducers such as functional polymers, for example, oleyl amides, organic compounds based on polyether and amide, 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 attack by metals, which function as chelating compounds, radical decontaminants, UV converters, layer forming agents reaction and more.
    Solid lubricants can be selected, for example, from the group of polymeric powders such as polyamides, polyimides or PTFE, graphite, metal oxides, boron nitride, metal sulphides such as molybdenum sulphide, tungsten sulphide or sulphide mixtures with based on tungsten, molybdenum, bismuth, tin and zinc, inorganic salts of alkali and alkaline earth metals, such as calcium carbonate, sodium and calcium phosphates. Solid lubricants can 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 certain metal halides; oxide and hydroxide compounds of transition metals and alkaline earth metals and their carbonates or phosphates; soft metals and / or plastics. The advantageous desired lubricating properties can be adjusted with the use of lignosulfonates with the need to use solid lubricants. In many cases, solid lubricants can be omitted entirely, or at least significantly reduced. If solid lubricants are used, graphite is the most favorable.
    Lignosulfonate can be selected from calcium lignosulfonates having a molecular weight (Mw, average weight) greater than 10,000, particularly greater than 12,000 or even greater than 15,000 g / mol, for example, from 10,000 to 65,000 g / mol or 15000 to 65000 g / mol and particularly containing from 2 to 12% by weight, particularly from 4 to 10% by weight, of sulfur (calculated as elemental sulfur) and / or from 5 to 15% by weight, particularly from 8 to 15 % by weight of calcium (calculated Ca). In addition to calcium lignosulfonates, other alkaline earth lignosulfonates can also be used. The average molecular weight (average weight) is determined, for example, by size exclusion chromatography. A suitable method is the SEC-MALLS method as described in the article by GE Fredheim, SM Braaten and BE Christensen, “Comparison of molecular weight and molecular weight distribution of softwood and hardwood lignosulfonates” published in “Journal of Wood Chemistry and Technology”, Vol. 23, N ° 2, pages 197-215, 2003 and the article “Molecular weight determination of lignosulfonates by size exclusion chromatography and multi12 angle laser scattering” by the same authors, published in the “Journal of Chromatography A”, Volume 942 , edition 1-2, 4 January 2002, pages 191199 (mobile phase: Phosphate DMSO-SDS, stationary phase: Jordi-GlukoseDVB as described in 2.5). Calcium lignosulfonates 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 following composition:
    (a) 55 to 92% by weight, particularly 70 to 85% by weight, of base oil,
    (b) 0 to 40% by weight, particularly 2 to 10% by weight, of additives,
    c) 3 to 40% by weight, particularly 5 to 20% by weight, of soaps, and
    d) 0 to 20% by weight or 0.5 to 20% by weight, particularly 0.5 to 10% by weight, of complexing agents, and
    e) excess of Ca (OH) 2 , preferably from 0.01 to 2% by weight,
    f) 0.5 to 50, particularly 2 to 15% by weight, and particularly preferable 3 to 8% by weight of lignosulfonate, particularly calcium lignosulfonate, in each case in relation to the total composition, in which the components and their variants Preferred have been defined in the above.
    It has been observed that lignosulfonates function as structure-forming agents for water-resistant lubricating greases that also have properties such as a solid lubricant or anti-wear additives and aging stabilizers. At the same time, lignosulfonate has been found to have surprising synergistic effects with other solid lubricants, for example, with graphite or calcium carbonate.
    It was also observed that lignosulfonates serve as multifunctional components for lubricants. Due to the large number of polar groups and aromatic structures they contain, their polymeric structure and their low solubility in all types of lubricating oils, lignosulfonates are suitable for use not only as a thickening component, but also as solid lubricants in lubricating greases and lubricating pastes. Its sulfur content also enhances its EP / AW effect on lubricating greases and the phenolic structures provide an aging inhibiting effect.
    It is assumed that due to the large number of polymeric and aromatic polar units it contains, the structure of lignosulfonate is predominantly planar.
    Consequently, they are able to be deposited very well in the layer structures on the metal surfaces due to the effect of external friction and shear forces, because the aromatic nuclei of the lignosulfonate enter into a reciprocal action associative with the metal surface, and the pairs Metal friction pads are effectively and permanently separated from each other even under heavy loads and high pressures.
    If calcium lignosulfonate is added before the start of the reaction phase during the production of soap thickeners, in particular calcium complex soaps, it is not only the thickening effect of these soaps intensified with a high drop point, but anti-wear and lubrication protection effects of the corresponding lubricating grease formulations are also intensified. Consequently, it is beneficial for the distribution and effect of solid additives and lubricants if they are chemically or mechanically incorporated into the thickener structure as an additional structural 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 1214 hydroxystearic acid, or special complexing agents such as borates or salts of acetic acid, sebacic acid and azeleic acid to manufacture the greases of soap with high drop points, however, these substances have little or no additional effect as anti-wear protection additives and friction reduction. If Ca-lignin sulfonates are included, the use of these other components can be significantly reduced or even dispensed with altogether. The use of Ca-lignin sulfonates still offers the ability to formulate high-performance lubricating greases based on renewable raw materials and to abandon an additive-oriented chemistry that is harmful 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 lignosulfonates are used as the only additional thickener and at the same time the only component As an additive, lubricating greases are obtained which were produced almost exclusively on the basis of renewable raw materials, the only exception being the calcium hydroxide used for metal soaps. These greases protect against aging and wear, and have the effect of increasing the capture load and decreasing friction when lignosulfonates are included as a thickener.
    The lubricating greases according to the invention are particularly suitable for use on or for constant speed joint shafts, bearing bearings and gearbox housings.
    If the base oils used consist of easily biodegradable esters, such as those containing mainly renewable raw materials, lubricating greases are also suitable 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 speed joint shafts, the first lubrication grease was formulated using calcium lignosulfonate which differs from the prior art in that it ensures long operating life and good levels of efficiency entirely without use of MoS 2 and other organic and inorganic molybdenum compounds.
    The absence of other additives also serves to reduce the friction coefficient, protect against capture load and wear and make the product highly compatible with the materials used in commercial standard constant speed shaft bellows, such as chloroprene rubber and thermoplastic polyether esters. Since the sulfur contained in lignosulfonate is bound by thermally stable sulfonate groups, unlike sulfur bound in conventional additives that is only released at very high temperatures and / or with very high levels of activation energies, the same does not occur in applications of lubricating grease except with tribocontacts under very high loads. In this way, the subsequent vulcanization or crosslinking of rubber materials by the sulfur released from the aging of the lubricant is largely prevented.
    If calcium lignosulfonate is used in a lubricating grease formulation that has been adjusted with excess calcium hydroxide to be more basic, this prevents free lignosulfonic acid from having a hydrolytic effect on materials used in the bellows, such as esters thermoplastic polyethers.
    A special aspect of the present invention is that it can be used to obtain cost-effective lubricating grease formulations for lubricating points that are under heavy load, such as constant speed joints in particular, and that are well compatible with the bellows containing, for example, thermoplastic polyether esters (TPE) and chloroprenes (CR), while offering a high degree of efficiency, low wear and long service life.
    Production examples
    Example A (comparison example):
    958 g of tallow fatty acid, 958 g of bovine tallow, 958 g of calcium acetate, 27.7 g of trisodium phosphate, 27.7 g of calcium borate and 358 g of calcium hydroxide were placed in a reactor in 12000 g of a mixture of base oil and 150 ml of water were added. This base was heated to 198 ° C in a defined temperature program while stirring so that the added water and the reaction water evaporated. Additives (see Table) were added to the base at certain temperatures during the cooling phase. Then the base was adjusted to the desired consistency by adding 3700 g of the base oil mixture, the final product was homogenized in a toothed colloid mill. The grease thus obtained is suitable for use as a constant speed joint shaft grease, for example.
    Example B:
    460 g tallow fatty acid, 445 g beef tallow, 460 g calcium acetate, 27.7 g trisodium phosphate, 27.7 g calcium borate and 168 g calcium hydroxide and 920 g calcium lignosulfonate (Norlig 11D powder manufactured by Borregard Lignotech) were placed in a reactor in 14000 g of a mixture of base oil and 150 ml of water were added. This base was heated to 208 ° C in a defined temperature program while stirring so that the added water and the reaction water evaporated. Additives (see Table) were added to the base at certain temperatures during the cooling phase. Then the base was adjusted to the desired consistency by adding 3450 g of the base oil mixture, the final product was homogenized in a toothed colloid mill. The grease thus obtained is suitable for use as a constant speed joint shaft grease, for example.
    Example C (comparison example):
    800 g 12-hydroxy stearic acid, 288 g of sebacic acid, 388 g of calcium acetate and 157.3 g of calcium hydroxide were placed in a reactor in 5000 g of a mixture of base oil. 64 g of LiOH x H 2 O were dissolved in 250 ml of water and added. This base was heated to 200 ° C in a defined temperature program 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.
    After the base was adjusted to the desired consistency by adding 3116 g of the base oil mixture, the final product was homogenized in a toothed colloid mill. The grease thus obtained is suitable for use as a bearing grease, for example.
    Example D:
    600 g of 12-hydroxy-stearic acid, 216 g of sebacic acid, 291 g of calcium acetate and 720 g of calcium hydroxide and 300 g of calcium lignosulfonate (Norlig 11D powder manufactured by Borregard Lignotech) were placed in a reactor in 5000 g of a mixture of base oil. 48 g of LiOH x H 2 O were dissolved in 250 ml of water and added. This base was heated to 200 ° C in a defined temperature program 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. After the base was adjusted to the desired consistency by adding 3116 g of the base oil mixture, the final product was homogenized in a toothed colloid mill. The grease thus obtained is suitable for use as a bearing grease, for example.
    Example E (comparison example):
    1380 g of tallow fatty acid, 1360 g of bovine tallow, 80 g of trisodium phosphate, 80 g of calcium borate, 1400 g of calcium acetate and 493 g of calcium hydroxide were placed in a reactor in 12000 g of a mixture of base oil and 150 ml of water were added. This base was heated to 230 ° C in a defined temperature program while stirring so that the added water and the reaction water evaporated. Additives (see table) 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 homogenized in a toothed colloid mill. The grease thus obtained is suitable for use as a bearing grease, for example.
    Example F:
    1260 g tallow fatty acid, 1240 g beef tallow, 80 g trisodium phosphate, 80 g calcium borate, 1278 g calcium acetate, 493 g calcium hydroxide and 885 g calcium lignosulfonate (Norlig 11D powder manufactured by Borregard Lignotech) were placed in a reactor in 12000 g of a mixture of base oil and 150 ml of water were added. This base was heated to 225 ° C in a defined temperature program 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. After the base was adjusted to the desired consistency by adding 3125 g of the base oil mixture, the final product was homogenized in a toothed colloid mill. The grease thus obtained is suitable for use as a bearing grease, for example.
    Example G (comparison example):
    975 g of hydroxy calcium-12 stearate, 225 g of calcium acetate and 15 g of calcium borate were placed in a reactor in 3500 g of methyl oleate ester. This base was heated to 200 ° C in a defined temperature program 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 of methyl oleate ester, the final product was homogenized in a 3-roll mill. The lubricating grease thus obtained is produced on the basis of predominantly renewable raw materials.
    Example H:
    841 g of 12-hydroxy calcium stearate, 219.5 g of calcium acetate, 15 g of calcium borate and 418 g of calcium lignosulfonate (Norlig 11D powder manufactured by Borregard Lignotech) were placed in a reactor in 1965 g of methyl oleate ester. This base was heated to 200 ° C in a defined temperature program 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 1684 g of trimethylolpropane trioleate ester, the final product was homogenized in a 3-roll mill. The lubricating grease thus obtained is produced on the basis of predominantly renewable raw materials.
    Examples I and J:
    The products of the formulations of example I and J are similar in the production of example H, but with the use of different amounts of hydroxy calcium-12 stearate, calcium acetate and calcium lignosulfonate and different ester base oil compositions. The lubricating greases thus obtained are produced on the basis of predominantly renewable raw materials.
    Table 1: Joint shaft grease formulations
    Example THEReference BInvention description Calcium complex Calcium complex with 6% with MoS2 lignosulfonate 1. Thickener:1.1 Lignosulfonate: Calcium lignosulfonate1.2 Fatty acids / - 0.0 6.1 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 Borate2. Base oils:Basic mineral oil 0.1 0.2 mixed (in v40 = 100 mm 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 Total4. Features Method unity 100 100 4.1 General physical data Penetration not worked Penetration worked 60 DIN ISO 2137 0.1 mm 263 315 double cyclesCopper corrosion 24h / 100 DIN ISO 2137 0.1 mm 351 340 ° C DIN51811 Assessment level 1-100 1-100 Drop pointOil separation 18 h / 40 DIN ISO 2176 ° C 240 280 ° C DIN51817 % 0.4 2.1 Oil separation 7 d / 40 ° C 4.2 Water resistance Static water resistance DIN51817 % 2 8.9 3 h / 90 ° C DIN 51807-1 Assessment level 1-90 1-90 Loss by washing at 80 ° C DIN 51807-2 Assessment level 1 1
    Table 1: (continued) Joint shaft grease formulations
    Example THE B Reference Invention description Calcium complex Calcium complex with MoS2 with 6% lignosulfonate 4.3 SRV friction reduction at 80 ° C (40 Hz f 1.5 m amplitude, 500 N load) Friction coefficient ASTM D D5707-05 0.107 0.097 Process constant constant SRV at 150 ° C (40 Hz, 1.5 mm amplitude, 500 N load)Coefficient of friction ASTM D D5707-05 0.097 0.085 Process4.4 Wear protection constant constant VKA Welding load DIN 51350-4 N 3400 3800 N VKA small cap 1000 N / l min4.5 Compatibility with bellows materials DIN 51350-5 mm 1.02 0.62 4.6.1 Chloroprene Inepsa 4012 168h / 120 ° C - Support A DIN 53505 -2 -1 - Volume change DIN 53521 % +3.5 -0.5 - Change in traction force DIN 53504 % -0.5 -1.2 - Change in stretching4.6.2 NBR rubber DIN 53504 % -22.1 -19 SRE NBR 34 7d / 100 ° C DIN 53538-3 - Support A DIN 53505 -2 -3 - Volume change DIN 53521 % +3.4 + 3.1 - Change in traction force DIN 53504 % -2.9 -5 - Change in stretching4.6.3 TPE elastomer DIN 53504 % -7.8 -4.5 Hytrel 8332 336h / 125 ° C - Support D DIN 53505 -3 -2 - Volume change DIN53521 % +13.1 + 6.2 - Change in traction force DIN 53504 % -32.9 + 6.7 - Change in stretchingAmitel EB 463 336h / 125 ° C DIN 53504 % -27 + 61 - Support D DIN 53505 -6 0 - Volume change DIN 53521 % +10.7 +10.2 - Change in traction force DIN 53504 % -15 -19.7 - Change in stretching4.6.4 EPDM rubber DIN 53504 % -10 + 7.8 Vamac Y76HR 336h / 125 ° C - Support A DIN 53505 +3 + 5 - Volume change DIN 53521 % +6 + 0.3 - Change in traction force DIN 53504 % -17.4 -1 = 8 - Change in stretching5. Test life on the gasket shaft DIN 53504 % -39 -35 constant speed about bearings Lifespan (mill.) 13.6 11.2 Mean steady-state temperature ° C 41.1 38.8
    U-l s> · ví ví ví <o rí t fO Η, Μ Γ ·! ΓΊ VÍ θ ’[C θ 'θ' θ’ ο
    'O
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    Q
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    5J5 VIDEO
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    ΟΟ μ η, θ 'θ'
    Table 2: Bearing bearing grease formulations
    Example
    «Õ ο
    Í2 .ο η _, ^ g§ <r .y ri J Ο
    Table 2: (continued) Bearing bearing grease formulations
    Example C D E F
    Reference Invention Reference Invention
    Complex of Complex of Complex of
    Description calcium / lithium calcium / lithium Calcium calcium / lithium complexes
    S 2 o and o oo o
    '5th
    -o o
    O
    CM σΊ 'Sf k »co κ> o - CM CM o os o
    CM °
    Mt
    05 O 05 S r ~ 05 m - T
    CM CM CM - 1st
    W1 T ._ „_. - 05 „
    CN CM CM CM Tf
    O 50 (M 05 T-I or f-5 wheel
    CM CM CM [2 U O O O oo oo cw t «<zi r- £ i-H I — I I — i Kl Kl
    SSSSS
    OOOOQ
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    O O wj irf
    2 * (0 ra t t o o 00 00
    O o 05 <N O o κι Ki κι κι κ> κι κι as s as d a o o a i-i oo
    Table 3: Formulations of lubricating grease with base oils from renewable raw materials
    Example G Η I J
    Reference Invention Reference Invention
    Description calcium complex calcium complex calcium complex calcium complex
    OO CM CM 'O
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    CM ro i CM © © OO CM ° σ c <
    hi hi
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    g £ cn O
    CM laughs O
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    CM CM, © «Ο 50 00 Çc CM ° m cn 'f' θ 'o CM O
    O - 'OO CM - CM
    O © 50
    CM CM CM O O oo Ο Ξο oo tzi ϊλ rb rz i — i i— * C, Μ V) Ι / Ί ssssss
    QQDnao ro
    OO
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    Q Q
    权利要求:
    Claims (24)
    [1]
    1. Process for producing lubricating greases containing ligninosulfonates, characterized by the fact that it comprises:
    a) the mixing stage of:
    - at least one base oil
    - at least one calcium soap of a saturated or unsaturated monocarboxylic acid having 10 to 32 carbon atoms, optionally substituted,
    - at least one complexing agent selected from:
    (i) an alkaline salt, with the exception of sodium salt, an alkaline earth salt, an aluminum salt, hydrocarboxylic acids or a saturated or unsaturated monocarboxylic acid having from 2 to 16 carbon atoms, each being optionally substituted , (ii) an alkaline or alkaline earth salt of boric acid and / or phosphoric acid, including their reaction products with LiOH and / or Ca (OH) 2 , and (iii) mixtures thereof, and
    - at least calcium lignosulfonate having average molecular weights (average weight) greater than 10,000 g / mol, heating above 120 ° C to initiate the reaction and expel components having a low boiling point to produce a base grease, and
    b) the step of cooling and adding base oil and possibly additives while mixing.
    [2]
    Process according to claim 1, characterized in that in step a) calcium hydroxide is added in addition to any other alkaline earth hydroxides.
    [3]
    Process according to claim 1, characterized in that the lubricating grease is adjusted with respect to alkalinity, particularly by adding an excess amount of calcium hydroxide.
    [4]
    Process according to claim 1, characterized by the fact that the heating occurs at temperatures higher than 180 ° C.
    [5]
    Process according to claim 1, characterized by the fact that in step a) lithium hydroxide, magnesium hydroxide and / or aluminum hydroxide and / or aluminum alcoholates and / or aluminum oxoalcoholates and / or lithium soaps , magnesium and / or aluminum of a saturated or unsaturated monocarboxylic acid having 10 to 32 carbon atoms, optionally substituted, are also used in addition to calcium hydroxide.
    [6]
    6. Process according to claim 1, characterized by the fact that the lubricating grease contains, independently of each other:
    from 55 to 92% by weight, particularly from 70 to 85% by weight of base oil, from 0 to 40% by weight, particularly from 2 to 10% by weight of additives,
    - from 3 to 40% by weight, particularly from 5 to 20% by weight, of soaps, and from 0.5 to 10% by weight, of complexing agents, and optionally excess of Ca (OH) 2, preferably 0 , 01 to 2% by weight,
    - from 0.5 to 15% by weight, and particularly preferable from 4 to 8% by weight of calcium lignosulfonate, optionally in addition to other alkaline earth lignin sulfonates, in each case in relation to the total composition of the lubricating grease.
    [7]
    7. Process according to claim 1, characterized by the fact that the base grease from step a) can be produced using
    40 to 70% by weight, particularly 45 to 60% by weight of base oil,
    10 to 60% by weight, particularly 15 to 50% by weight, of soaps, and
    - 5 to 30% by weight, of complexing agent, and optionally excess Ca (OH) 2, preferably from 0.02 to 4% by weight, and
    0.7 to 30% by weight of calcium lignosulfonate, optionally in addition to other alkaline earth lignin sulfonates, in each case in relation to the composition of the base grease.
    [8]
    Process according to claim 1 or 4, characterized in that the base grease contains, independently of each other, from 0.2 to 5% by weight of graphite and / or no solid lubricant or less than < 1% by weight of solid lubricant, particularly no M0S2.
    [9]
    Process according to claim 1, characterized in that the calcium soap is produced in situ as a by-product of the reaction of calcium hydroxide with a saturated or unsaturated monocarboxylic acid having 10 to 32 carbon atoms, particularly having from 16 to 20 carbon atoms, optionally substituted, for example, by hydroxy, as an ester or anhydride.
    [10]
    Process according to claim 1, characterized in that the complexing agent as a product of the reaction of a calcium salt, particularly of calcium hydroxide, with a saturated or unsaturated monocarboxylic acid having from 2 to 8, particularly of 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 replaced, for example, by hydroxyl as an ester or anhydride, is added during step a).
    [11]
    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, particularly from 2 to 4, carbon atoms or a dicarboxylic acid having from 2 to 16, particularly from 2 to 12 carbon atoms, each of which may or may not be replaced, for example, by hydroxyl as an ester or anhydride.
    [12]
    12. Process according to at least one of claims 1 to 11, characterized by the fact that calcium lignosulfonate is drained to less than 0.5% by weight of water before being added, for example, by means of heating in the base oil above 95 ° C, particularly above 100 ° C, for example, to 120 ° C.
    [13]
    Process according to at least one of claims 1 to 12, characterized in that the composition contains from 0.5 to 20% by weight, particularly from 0.5 to 10% by weight of the complexing agent.
    [14]
    14. Lubricating grease composition, characterized by the fact that it contains:
    from 55 to 92% by weight, particularly from 70 to 85% by weight, of base oil, from 0 to 40% by weight, particularly from 2 to 10% by weight, from additives, from 3 to 40% by weight, particularly from 5 to 20% by weight, of calcium soaps of a saturated or unsaturated monocarboxylic acid having from 10 to 32 carbon atoms, optionally substituted, from 0.5 to 10 ° / o by weight, of complexing agent, selected from :
    (i) an alkaline salt, with the exception of sodium salt, an alkaline earth salt or aluminum salt, a saturated or unsaturated monocarboxylic acid or hydrocarboxylic acids having from 2 to 8 carbon atoms, a dicarboxylic acid having from 2 to 16 carbon atoms, each optionally substituted, (ii) an alkaline or alkaline earth salt of boric acid and / or phosphoric acid, including the reaction products thereof with LiOH and / or Ca (OH) 2 , optionally excess Ca (OH) 2 , preferably 0.01 to 2% in feet, and (iii) mixing thereof, and
    - 0.5 to 15% by weight, and particularly preferably from 2 to 8% by weight of calcium lignosulfonate possibly in addition to other alkaline earth lignisulfonates, in each case in relation to the total composition of the lubricating grease, wherein the composition comprises a cone penetration value (penetration worked) from 265 to 385 mm / 10 (at 25 ° C), determined according to ISO 2137.
    [15]
    15. Composition according to claim 14, characterized in that the composition comprises a cone penetration value (penetration worked) from 285 to 355 mm / 10, determined according to ISO 2137.
    [16]
    Composition according to at least one of claims 14 or 15, characterized in that the base oil has a kinematic viscosity of 20 to 2500 mm 2 / s, preferably 40 to 500 mm 2 / s, in 40 ° C.
    [17]
    17. Composition according to at least one of claims 14 to 16, characterized by the fact that the complexing agent consists of:
    an alkali salt, preferably lithium salt, alkaline earth salt, preferably calcium salts, or aluminum salt of a saturated or unsaturated monocarboxylic acid having from 2 to 8, in particular from 2 to 4,
    5 carbon atoms or a dicarboxylic acid having from 2 to 16, particularly from 2 to 12, carbon atoms, each of which may or may not be substituted.
    [18]
    18. Composition according to at least one of claims 14 to 17, characterized by the fact that the additive
    10 comprises one or more members selected from the following group:
    amine compounds, phenol compounds, sulfur antioxidants, zinc dithiocarbamate or zinc dithiophosphate as antioxidants;
    organic compounds of chlorine, sulfur borate, phosphorus or calcium, zinc dithiophosphate, organic compounds of bismuth as
    15 high pressure additives;
    C2 to C6 polyols, fatty acids, fatty acid esters or animal or vegetable oils;
    petroleum sulfonate, dinonylnaphthalene sulfonate or sorbitan esters as anti-corrosion agents;
    20 - benzotriazole or sodium nitrite as metal neutralizers;
    polymethacrylate, polyisobutylene, oligodec-l-enes, and polystyrenes as viscosity enhancers;
    - dialkyl dithiocarbamate molybdenum or dialkyl dithiocarbamate molybdenum 25, aromatic amines as anti-wear additives,
    - functional polymers, for example oleyl amides, organic compounds based on polyether and amide, or molybdenum dithiocarbamate as friction modifiers, and
    - polymeric powders, such as polyamides, polyimides or
    Ί
    PTFE, graphite, metal oxides, boron nitride, metal sulfides such as molybdenum disulfide, tungsten disulfide or mixed sulfides based on tungsten, molybdenum, bismuth, tin and zinc, inorganic salts of alkali and alkaline earth metals, such as calcium carbonate, phosphates
    5 sodium and calcium as solid lubricants.
    [19]
    19. Composition according to at least one of claims 14 to 18, characterized by the fact that the lubricating grease is water resistant, particularly:
    a) according to the test defined in DIN 51807-1, level 10 assessment from 1 to 90, and / or
    b) according to the test defined in DIN 51807-2, evaluation level from 1 to 80.
    [20]
    20. Composition according to at least one of claims 14 to 19, characterized by the fact that lignosulfonate of
    15 calcium has an average molecular weight (Mw, average weight) of more than 10,000, particularly more than 12,000, or even more than 15,000 g / mol, and regardless of these it contains 2 to 12% by weight, particularly 4 10% by weight of sulfur (calculated as elemental sulfur) and / or also independently from 5 to 15% by weight,
    20 particularly 8 to 15% by weight of calcium.
    [21]
    21. Composition according to at least one of claims 14 to 20, characterized in that the lubricating grease contains a base oil based on renewable raw materials and / or a fraction of 95% or more of these is produced on the basis of
    25 renewable raw materials.
    [22]
    22. Composition according to at least one of claims 14 to 20, characterized by the fact that the composition has a drop point greater than 200 ° C according to DIN ISO 2176.
    [23]
    23. Use of a composition as defined in any one of claims 14 to 22, characterized in that it is for lubricating at least one transmission.
    [24]
    24. Use of a composition as defined in any of claims 14 to 22, characterized in that it is for lubricating
    5 lubrication points on constant speed joints that have a joint shaft dome material.
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    同族专利:
    公开号 | 公开日
    DE102010006745A1|2011-08-04|
    PT2531587E|2016-02-26|
    PL2531587T3|2016-06-30|
    KR101833854B1|2018-03-05|
    RU2554873C2|2015-06-27|
    CA2788157A1|2011-08-11|
    RS54610B1|2016-08-31|
    DK2531587T3|2016-01-25|
    AU2011212763B2|2013-10-17|
    AU2011212763A1|2012-09-06|
    EP2531587B9|2016-10-05|
    HRP20160072T1|2016-04-08|
    SI2531587T1|2016-04-29|
    JP2013518929A|2013-05-23|
    EP2531587A1|2012-12-12|
    WO2011095155A1|2011-08-11|
    CA2788157C|2018-06-26|
    CN102770513A|2012-11-07|
    EP2531587B1|2015-11-04|
    RU2012136909A|2014-03-10|
    BR112012019181A2|2018-03-27|
    HUE026690T2|2016-07-28|
    ES2561821T3|2016-03-01|
    JP5856078B2|2016-02-09|
    MX2012008960A|2012-10-15|
    US20120302472A1|2012-11-29|
    KR20120139730A|2012-12-27|
    CN102770513B|2015-09-30|
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    法律状态:
    2018-07-03| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|
    2018-09-11| B16A| Patent or certificate of addition of invention granted|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 31/01/2011, OBSERVADAS AS CONDICOES LEGAIS. |
    2019-06-11| B25D| Requested change of name of applicant approved|Owner name: FUCHS PETROLUB SE (DE) |
    优先权:
    申请号 | 申请日 | 专利标题
    DE102010006745.8|2010-02-02|
    DE102010006745A|DE102010006745A1|2010-02-02|2010-02-02|Greases containing lignosulfonate, their preparation and use|
    PCT/DE2011/000087|WO2011095155A1|2010-02-02|2011-01-31|Lubricating greases containing lignosulfonate, the production thereof, and the use thereof|
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