C10N2030/64

LUBRICANT COMPOSITION AND USE OF THE SAME AS A PIPE DOPE

The present invention provides a lubricant composition comprising: (i) a base oil (ii) an organophilic clay-based thickener; and (iii) a solid lubricant, wherein said solid lubricant does not comprise any heavy metals. The present invention also provides the use of a lubricant composition comprising: a base oil; an organophilic clay-based thickener; and a solid lubricant, wherein said solid lubricant does not comprise any heavy metals, as a pipe dope.

Use of oils comprising non-neurotoxic anti-wear additives

The invention relates to the use of an oil that does not include tricresyl phosphate and includes as an anti-wear additive at least one diphosphorus compound for the prophylaxis of aerotoxic syndrome, especially in case of fume event. It also relates to the oil as such.

USE OF OILS COMPRISING NON-NEUROTOXIC ANTI-WEAR ADDITIVES

Disclosed is an oil that does not include tricresyl phosphate and includes as an anti-wear additive at least one diphosphorus compound for the prophylaxis of aerotoxic syndrome, especially in case of fume event. It also relates to a lubrication method utilizing such oil.

REFRIGERANT-CONTAINING COMPOSITION, AND REFRIGERATING METHOD, REFRIGERATING DEVICE OPERATING METHOD, AND REFRIGERATING DEVICE USING SAID COMPOSITION

The present disclosure provides a composition comprising a refrigerant characterized by having a coefficient of performance (COP) and a refrigerating capacity (Capacity) equivalent to or higher than those of R134a, and having a sufficiently low GWP. The present disclosure is, specifically, a composition comprising a refrigerant, the refrigerant comprising cis-1,2-difluoroethylene (HFO-1132(Z)) and 2,3,3,3-tetrafluoropropene (HFO-1234yf), wherein HFO-1132(Z) is present in an amount of 53.0 to 59.5 mass %, and HFO-1234yf is present in an amount of 47.0 to 40.5 mass %, based on the total mass of IFO-1132(Z) and HFO-1234yf.

ALKYLBENZENE SULFONATE DETERGENTS

The instant disclosure relates to hydrocarbyl- (e.g., alkyl-) benzene sulfonate detergents and their salts, where the hydrocarbyl group includes moieties equivalent to 5 to 10 carbon branched polyene compounds. Such compounds and their salts are useful as lubricant additives. The detergents disclosed herein may solve at least one problem of providing anti-wear performance, frictional performance, oxidation performance, viscosity performance, and detergency.

BIODEGRADABLE FLUIDS

The incorporation of highly refined, low viscosity index base oils along with a polymeric thickener produces a final readily biodegradable fluid with a significantly high viscosity. The present invention allows the formulation of a high viscosity readily biodegradable fluid where the vast majority of the fluid is mineral oil. Previous uses of mineral oils only allowed for formulation of substantially lower viscosity readily biodegradable fluids.

BIODEGRADABLE LUBRICANT WITH TAILORED HYDROLYTIC STABILITY AND IMPROVED THERMAL STABILITY THROUGH ALKOXYLATION OF GLYCEROL

Described herein are methods of stabilizing the beta hydrogen of glycerol based esters by the insertion of alkoxy groups to significantly improve the thermal, oxidative, and hydrolytic stability of the ester and allow for controlling the molar density of esters bonds in the lubricants to maximize hydrolytic stability while maintaining biodegradability and further improving performance properties.

Lubricating oil additive and lubricating oil composition containing same

The present invention provides a lubricating oil additive, including: a molybdenum compound (A) represented by the following general formula (1); and a sulfur-based composition (B) containing a sulfur-based compound (b-1) represented by the following general formula (2) and at least one kind of sulfur-based compound (b-2) represented by the following general formula (3) or (4), and a lubricating oil composition containing the additive. In the formula (1), R.sup.1 to R.sup.4 each represent alkyl groups having 6 to 18 carbon atoms, the groups being identical to or different from each other, and X.sup.1 to X.sup.4 each independently represent an oxygen atom or a sulfur atom. In the formula (2), R.sup.5 represents an alkyl group having 1 to 22 carbon atoms, R.sup.6 represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms, R.sup.7 represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms, and “a” represents a number from 1 to 10. In the formulae (3) and (4), R.sup.8 to R.sup.11 each represent alkylene groups having 1 to 28 carbon atoms, the groups being identical to or different from each other, R.sup.12 and R.sup.13 each independently represent a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, and “b” and “c” each independently represent a number from 1 to 8, provided that at least one of R.sup.12 or R.sup.13 represents an alkyl group having 1 to 3 carbon atoms. ##STR00001##

Base oil synthesis via ionic catalyst oligomerization and waterless separation of the oligomerization catalyst

Described herein is a base oil synthesis via ionic catalyst oligomerization further utilizing a hydrophobic process for removing an ionic catalyst from a reaction mixture with a silica gel composition, specifically a reaction mixture comprising an oligomerization reaction to produce PAO utilizing an ionic catalyst wherein the ionic catalyst is removed post reaction.

Lubricant compositions, and synthesizing methods and applications of same

A lubricant composition includes a base lubricant and a plurality of lubricant additive molecules functioning as precursor molecules to induce tribopolymerization and forming in situ protective tribofilm with desirable robustness and low shear resistance. Each lubricant additive molecule includes one or more surface-active groups attractable to target surface, and a carbon containing component operable connected to the one or more surface active groups. The carbon containing component comprise a carbon ring structure having a high ring strain that is metastable and activatable with a ring-opening reaction. A less stable carbon ring structure is more readily activated to the intermediate state, preferable to form more active fragments. Increasing the adsorption strength further is beneficial to prolonging the residence time of additive molecules on the target surface, thereby facilitating the dissociation of molecules and subsequent polymerization.