Abstract: Disclosed are systems and methods for generating graphical displays of analyte data and/or health information. In some implementations, the graphical displays are generating based on a self-referential dataset that are modifiable based on identified portions of the data. The modified graphical displays can indicate features in the analyte data of a host.

Abstract: A polyurethane composition, which contains at least one isocyanate-group-containing polymer, obtained from the reaction of at least one polyol with at least one diisocyanate, and at least one oxazolidine of the formula (I). The polyurethane composition allows one-component moisture-curing adhesives, sealants or coatings that have good storage stability, long open times and cure quickly to give a surprisingly non-tacky material having pronounced high-resilient properties.

Abstract: Disclosed are systems and methods for generating graphical displays of analyte data and/or health information. In some implementations, the graphical displays are generating based on a self-referential dataset that are modifiable based on identified portions of the data. The modified graphical displays can indicate features in the analyte data of a host.

Abstract: A vehicle roof having a roof skin assembly, a roof substructure, which is disposed below the roof skin assembly, and at least one sensor module having at least one environment sensor for detecting a vehicle environment, the environment sensor being disposed in a sensor housing having a sensor window. The roof skin assembly has a sensor cutout accommodating the sensor housing in a circumferentially sealing manner with the result that the sensor window forms a visible outer roof surface.

Abstract: A vehicle roof, in particular of a passenger car, having a roof cladding arrangement and a roof substructure, which is at least partially covered by the roof cladding arrangement, and at least one environment sensor for charting a vehicle environment and another electrical installation for emitting and/or receiving electromagnetic radiation, characterized in that the roof cladding arrangement comprises a visor which has a groove-free outer visible surface, in that the environment sensor and the other electrical installation are disposed beside each other or above one another behind and/or below the visor and in that the visor has a first transmission area having a first transmission behavior for the environment sensor and a second transmission area having a second transmission behavior for the other electrical installation, the second transmission behavior differing from the first transmission behavior.

Abstract: A method of calculating a collision point between an ego vehicle and a target vehicle and to emergency-brake-assist deceleration using the calculation. The calculation defines areas of collision risk of the ego vehicle, determines movement of the ego and target vehicle, calculates times-to-collision for first and second ego-vehicle intersecting points and a target-vehicle intersecting point to an intersection point. A risk collision point condition establishes that the collision point is inside an ego vehicle area if the first time-to-collision for the first ego-vehicle intersecting point reaching the intersection point is less than a third time-to-collision for the target-intersection point reaching the intersection point, and the second time-to-collision for the second ego-vehicle intersecting point reaching the intersection point is greater than the third time-to-collision for the target intersection point reaching the intersection point.

Abstract: An amine-functional adduct from the reaction of at least one amine of the formula (I) with at least one novolak epoxy resin having an average functionality in the range from 2.5 to 4. The adduct is liquid at room temperature without thinners and without a large excess of amine. It is suitable as a curing agent for epoxy resin compositions, in which it permits good workability, rapid curing, high hydrophobicity, and a high crosslinking density. It is particularly suitable for coatings, in which it permits nice surfaces, good intercoat adhesion, high thermal shock resistance, and good protection against steel corrosion.

Abstract: A moisture-curing polyurethane composition including: at least one isocyanate-functional polymer with a content of monomeric isophorone diisocyanate of below 0.5 weight-%, obtained from the reaction of isophorone diisocyanate and at least one polyol, and at least one aldimine of formula (I). The composition has a low toxicity, good shelf life stability and cures quickly to an elastic material of low surface tack and good mechanical properties, particularly in terms of high tensile strength and modulus of elasticity at high elongation. It enables coatings, sealants and adhesives with excellent stability under outdoor weathering conditions and high UV load. The aldimine of formula (I) allows to overcome the drawbacks caused by the removal of most of the monomeric isophorone diisocyanate in terms of cure speed, surface tackiness and final strength of such compositions.

Abstract: A mixture of isomeric aldimines of the formulae (Ia), (Ib) and (Ic) in which the ratio of the trans,trans isomer (Ia) to the sum of the cis,trans isomer (Ib) and the cis,cis isomer (Ic) is in the range of 5/95 to 30/70, and its use as latent hardener for moisture-curing isocyanate-functional polyurethane compositions. The inventive mixture of isomeric aldimines enables polyurethane compositions with very low content of monomeric isophorone diisocyanate and excellent stability under outdoor wheathering conditions and high UV load, which cure quickly to an elastic material of low surface tack and good mechanical properties, particularly in terms of high tensile strength and modulus of elasticity at high elongation. Such compositions are particularly suitable as elastic adhesives and/or sealants or elastic coatings, particularly for outdoor use such as on roofs, floors or ships.

Abstract: An estimated initial direction of movement of a newly-detected object is to be determined. The actual previous directions of movement and positions of previously-detected objects are determined and stored. When a newly-detected object is newly detected at a certain position, then the actual previous direction of movement of one of the previously-detected objects at that position is used as a basis to determine the estimated initial direction of movement of the newly-detected object at that position.

Abstract: A curing agent for epoxy resins has N-benzylethane-1,2-diamine and N,N?-dibenzylethane-1,2-diamine in a weight ratio in the range from 65/35 to 95/5. The curing agent is easy to prepare, thins epoxy resins particularly well, and enables low-emission epoxy resin products that have good workability and a long pot-life, cure reliably and surprisingly fast and can be walked on after a short time, in particular even in cold conditions. Coatings of particularly high mechanical grade, with a high surface quality and a minimal tendency to yellowing, can thus be produced. Epoxy resins of this type are particularly suitable for coating floors.

Abstract: A curing agent for epoxy resins, including 1-amino-3-aminomethyl-3,5,5-trimethylcyclohexane and N-benzyl-1,2-ethandiamine in an amount for the ratio of the number of its amine hydrogens to be in the range of 90/10 to 20/80. The curing agent permits suitable epoxy resin compositions that have excellent workability and that cure particularly rapidly in cold and damp conditions, without blushing-induced surface defects, thus achieving coatings of in particular high hardness, high glass transition temperature and surprisingly little tendency to yellowing.

Abstract: An amino-functional addition product from the reaction of at least one diamine of the formula (I) with at least one aromatic diepoxide in a stoichiometric ratio in the range of 1.3 to 1.7 mole diamine per 1 mole-equivalent of epoxy groups. The addition product is liquid at room temperature without a diluent and has surprisingly low viscosity. The composition allows the manufacture of low-emission epoxy-resin coatings that have good workability, cure particularly rapidly and with high surface quality in cold and damp conditions, and allow for a wide range of combinations with other amines and diluents.

Abstract: A silane group-containing polymer obtained from reacting (i) an isocyanate group-containing polymer having an NCO content in the range of 0.3 to 4% by weight and a monomeric diisocyanate content of at most 0.3 wt. % obtained from the reaction of at least one monomeric diisocyanate with at least one polyether polyol in a molar NCO/OH ratio of at least 3/1 and subsequent removal of a major part of the unreacted monomeric diisocyanates by means of a suitable separation process, (ii) with at least one amino-, mercapto- or hydroxysilane in a stoichiometric ratio of at least 1 mole of amino-, mercapto- or hydroxysilane per mole equivalent of isocyanate groups.

Abstract: An amine-functional adduct from the reaction of an amine mixture containing at least one diamine of formula (I) and at least one diamine of formula (II) in a weight ratio ranging from 65/35 to 95/5 with at least one diepoxide in a stoichiometric ratio of at least 1. 2 moles of diamine of the formula (I) to 1 mole equivalent of epoxide groups. The adduct is liquid at room temperature without diluent even in the presence of a small excess of diamine and is surprisingly low in viscosity. In addition, it is particularly cost-effective, as it is available from an amine mixture that is technically easy to produce. The adduct enables low-emission or emission-free epoxy resin coatings with surprisingly good workability at surprisingly fast curing, which have a high hardness and low tendency to yellowing, and which hardly tend to blushing-related defects even in cold and humid conditions.

Abstract: A branched polymer containing silane groups having an average of at least 2.1 silane groups per molecule, from the reaction of (i) a polymer containing isocyanate groups and having an NCO content ranging from 0.7% to 4% by weight, obtained from the reaction of at least one monomeric diisocyanate with at least one polyether polyol in a molar NCO/OH ratio of at least 1.5/1, (ii) with at least one amino-, mercapto- or hydroxysilane, in a stoichiometric ratio of at least 1 mol of amino-, mercapto- or hydroxysilane per molar equivalent of isocyanate groups. The polymer containing silane groups is storage-stable, liquid at room temperature and easily handled, and permits curable compositions having excellent processability, rapid curing, high strength coupled with good extensibility, and good thermal stability. It is particularly suitable as a constituent of moisture-curable sealants, adhesives or coatings, additionally including a further, in particular linear, polymer containing silane groups.

Abstract: A compound of formula (I) having advantageous properties when used as a latent curing agent for compositions containing isocyanate groups, and to compositions containing the compound of formula (I). The compound of formula (I) is odourless, is liquid and has comparatively low viscosity at room temperature and is stable in storage together with isocyanates. It makes possible odourless single-component polyurethane compositions which have good stability in storage, do not produce bubbles when cured in the presence of moisture, and cause no problematic odour emissions, giving a cured elastic material having good mechanical properties, good heat stability, a surprisingly non-adhesive surface and little tendency towards plasticizer migration.

Abstract: The use of an aldehyde mixture containing 70 to 95 wt % of aldehydes of formula (I) and 5 to 30 wt % of alkylbenzene compounds not corresponding to formula (I) as a blocking agent for amines results in odorless, especially economically blocked amines, which at room temperature are typically liquid and have a surprisingly low viscosity. Such blocked amines are particularly suitable as latent hardeners in isocyanate-group-containing compositions. Single-component moisture-curing polyurethane compositions formulated therewith are surprisingly stable in storage, can be used for low-emission applications without odor problems and do not trigger any problems with plasticizer migration. Surprisingly, said compositions even have advantages over corresponding compositions having latent hardeners based on purified aldehydes of formula (I), in particular with respect to viscosity, storage stability and especially strength.

Abstract: A process for preparing an aldol ester of the formula (I), wherein at least one carboxylic anhydride of the formula (II) is reacted with at least one aldol of the formula (III) with heating in the presence of a basic catalyst with a pKa of the conjugate acid of at least 8, and the reaction product obtained from the process. The process provides a light-coloured and low-odour reaction product which has a high content of aldol ester content of the formula (I) and can be used, without elaborate purification steps, particularly without overhead distillation of the aldol ester, as a blocking agent for primary amines. The resultant blocked amines have a long storage life together with polymers containing isocyanate groups, and cure rapidly and reliably on contact with moisture to form mechanically high-grade and robust elastomers.

Abstract: A curing agent for epoxy resin compositions containing at least one amine of formula (I) and at least one amine of formula (II). The curing agent is a low-odor, low-viscosity, low-toxicity curing agent and has a low propensity for carbamatization and a high reactivity toward epoxy resins. It enables low-odor and low-emission epoxy resin products which are readily processable and which even at low temperatures and high humidities undergo rapid and problem-free curing to afford high-quality plastics having a high hardness and a regular, non-tacky surface with high gloss.