Abstract: Provided is an apparatus for the automated synthesis of at least one chemical compound including: at least one cartridge including at least one first compartment for providing at least one first reagent for the chemical synthesis of the at least one compound; at least one second compartment for providing at least one second reagent for the chemical synthesis of the at least one compound, and at least one third compartment for purifying the at least one synthesized compound; at least one reaction container for providing the compounds to be fed into at least one of the compartments of the cartridge and/or collecting the reaction product from at least one of the compartments of the cartridge; at least one solvent container at least two flow path selecting valves and at least one pump.

Abstract: A method for predicting formation permeability by measuring diffusional tortuosity in several directions by pulse gradient NMR. The method comprises evaluating an anisotropic diffusion coefficient by pulsed gradient NMR, determining diffusional tortuosity from the restricted diffusion data, supplementing the NMR results with resistivity and sonic logging data, measuring anisotropic tortuosity and porosity by resistivity and sonic data and combining all components in a single fitting model. The 11-coefficient model is trained to recognize the true values of permeability by comparing the real oil permeabilities measured in a library of oil-carrying rock cores with the NMR, resistivity and sonic correlates. The fitting coefficients are extracted by minimizing the discrepancy between the laboratory measured permeabilities and the predicted values combining all rapid logging information components with the agreement-maximizing weights.

Abstract: A method for predicting formation permeability by measuring diffusional tortuosity in several directions by pulse gradient NMR. The method comprises evaluating an anisotropic diffusion coefficient by pulsed gradient NMR, determining diffusional tortuosity from the restricted diffusion data, supplementing the NMR results with resistivity and sonic logging data, measuring anisotropic tortuosity and porosity by resistivity and sonic data and combining all components in a single fitting model. The 11-coefficient model is trained to recognize the true values of permeability by comparing the real oil permeabilities measured in a library of oil-carrying rock cores with the NMR, resistivity and sonic correlates. The fitting coefficients are extracted by minimizing the discrepancy between the laboratory measured permeabilities and the predicted values combining all rapid logging information components with the agreement-maximizing weights.

Abstract: A sensor is driven at a first heating power value. The sensor generates a sensing signal that is indicative of a sensed entity. A possible onset of a sensor contamination condition is detected as a function of the sensing signal generated by the sensor. If such detecting fails to indicate onset of a sensor contamination condition, the sensor continues to be driven at the first heating power value. However, if such detecting indicates onset of a sensor contamination condition, a protection mode is activated. In the protection mode, the sensor is driven at a second heating power value for a protection interval, where the second heating power value is lower than the first heating power value. Furthermore, the operation may refrain from supplying power to the sensor for a further protection interval, wherein the further protection interval is longer than the protection interval.

Abstract: The present invention relates to a heat preservation shell (4) for an analyzer. At least one liquid passage (402) for conveying the liquid is embedded in a shell wall of the heat preservation shell. The liquid passage (402) is embedded in the shell wall of the heat preservation shell (4), on one hand, the liquid transported or preserved in the liquid passage is subjected to the heat preservation function of the heat preservation shell, so that the liquid transported or preserved in the liquid passage (402) maintains the preset temperature, thereby avoiding the influence of the external environment temperature on the transported liquid; and on the other hand, the space of the shell wall of the heat preservation shell is effectively utilized, the situation that various liquid pipelines are intricately distributed inside or outside the heat preservation shell (4) is avoided, thereby increasing the space utilization rate.

Abstract: A method for predicting formation permeability by measuring diffusional tortuosity in several directions by pulse gradient NMR. The method comprises evaluating an anisotropic diffusion coefficient by pulsed gradient NMR, determining diffusional tortuosity from the restricted diffusion data, supplementing the NMR results with resistivity and sonic logging data, measuring anisotropic tortuosity and porosity by resistivity and sonic data and combining all components in a single fitting model. The 11-coefficient model is trained to recognize the true values of permeability by comparing the real oil permeabilities measured in a library of oil-carrying rock cores with the NMR, resistivity and sonic correlates. The fitting coefficients are extracted by minimizing the discrepancy between the laboratory measured permeabilities and the predicted values combining all rapid logging information components with the agreement-maximizing weights.

Abstract: Methods for determining the catalytic activity of an activated chemically-treated solid oxide using a color measurement technique are described, and these methods are integrated into transition metal-based catalyst preparation processes and systems, as well as into olefin polymerization processes and related polymerization reactor systems.

Abstract: An abnormality diagnosis apparatus includes an irradiation device to detect a resonance frequency by irradiating an electromagnetic wave to the NOx catalyst, and a controller to diagnose based on the resonance frequency whether the NOx catalyst is abnormal, wherein the NOx catalyst is arranged in such a position that an electric field strength inside the NOx catalyst at the time when the irradiation device irradiates the electromagnetic wave of the resonance frequency becomes larger in an upstream portion of the NOx catalyst, which is at the upstream side of a center of the NOx catalyst in the direction of flow of exhaust gas, than in a downstream portion of the NOx catalyst, which is at the downstream side of the center of the NOx catalyst.

Abstract: The present disclosure provides natural gas and petrochemical processing systems, including oxidative coupling of methane reactor systems that may integrate process inputs and outputs to cooperatively utilize different inputs and outputs in the production of higher hydrocarbons from natural gas and other hydrocarbon feedstocks. The present disclosure also provides apparatuses and methods for heat exchange, such as an apparatus that can perform boiling and steam super-heating in separate chambers in order to reach a target outlet temperature that is relatively constant as the apparatus becomes fouled. A system of the present disclosure may include an oxidative coupling of methane (OCM) subsystem that generates a product stream comprising compounds with two or more carbon atoms, and a dual compartment heat exchanger downstream of, and fluidically coupled to, the OCM subsystem.

Abstract: A process for the laboratory deactivation of a porous solid comprising subjecting the porous solid to a cyclic treatment, the treatment being selected from a hydration/dehydration cyclic treatment, a thermal cyclic treatment, or combinations thereof.

Abstract: A method for operating a test station (10) for portable gas-measuring devices (20) is provided. The gas-measuring device (20) is arranged in fluid-communication with the test station (10) via at least one interface (13). A flow time is set, during which the test gas (30) is fed and a waiting time is set, during which no test gas (30) is fed. After an end of the feed of the at least one test gas results of the test are analyzed. The test station (10) is configured for feeding at least one test gas (30) to the interface (13). The test station (10) for portable gas-measuring devices (20) has at least one interface (13) for the fluid-communicating arrangement of the gas-measuring device (20), and wherein the test station (10) is configured for feeding at least one test gas (30) to the interface (13).

Abstract: A preparative liquid chromatographic apparatus comprising a column for separating components in a sample; a dispensing unit for dispensing an eluate from the column; a detector for the eluate; an analysis unit for the eluate; a display unit for displaying an analysis result a data storage unit; and an arithmetic control unit for controlling the display unit and the data storage unit. The analysis unit has at least one qualitative analysis unit for continuously and qualitatively analyzing the eluate. The display unit simultaneously displays a chromatogram acquired by the detector and the acquisition position of the dispensing unit and displays a correspondence relationship between each fraction and the chromatogram, and wherein by using the correspondence relationship between each fraction and the chromatogram shown in the display unit, the qualitative analysis data selected from the data storage unit is displayed on the display unit using the arithmetic control unit.

Abstract: A microfluidic diagnostic device may comprise a fluid inlet to receive a fluid from a fluidic slot, a main microfluidic channel fluidly coupled to the fluid inlet, and a main microfluidic pump interposed between the fluid inlet and the main microfluidic channel to continuously circulate a fluid through the fluidic slot, fluid inlet, and main microfluidic channel wherein the width of the fluid inlet is different from the width of the main microfluidic channel. A diagnostic device, comprising a fluidic slot, a fluid inlet fluidly coupled to the fluidic slot, a main channel fluidly coupled to the fluid inlet, and an inlet pump interposed between the fluid inlet and channel wherein the cross-sectional area of the fluid inlet is relatively larger at least one point than the cross-sectional area of the channel.

Abstract: Provided is a mixing device that is configured to install therein a multi-well plate including a plurality of wells capable of containing matter to be mixed and includes mixing mechanisms each of which mixes the matter to be mixed with a motor and is provided for each of the wells. The mixing mechanisms each includes a first rotator that is connected to the motor and rotates due to activation of the motor, a mixing rod that mixes the matter to be mixed, a second rotator that supports the mixing rod, a magnetic coupling mechanism that magnetically couples the first rotator to the second rotator, and a seal ring that surrounds an opening of the well and is capable of closing the well together with the second rotator.

Abstract: An internal combustion engine includes an upstream side exhaust purification catalyst and a downstream side exhaust purification catalyst. The control device includes a storage amount estimating device which estimates the oxygen storage amount of the downstream side exhaust purification catalyst, and can execute fuel cut control which cuts the feed of fuel to the combustion chamber during operation of the internal combustion engine when the engine speed is the lowest reference speed or more. The control device lowers the lowest reference speed when the storage amount estimated by the storage amount estimating device has become a given limit storage amount or less, compared with when it is larger than the limit storage amount. As a result, a control device can effectively keep the oxygen storage amount of the downstream side exhaust purification catalyst from decreasing to zero.

Abstract: Process for evaluating the catalytic performance of a porous solid using a vapor diffusion technique, where a probe molecule and a molecule for dead-time determination is injected into a carrier gas that is then contacted with the porous solid in a vessel, where a detector analyzes the peak width and retention time of a probe molecule and the retention time of the molecule for dead-time determination in the gas exiting the vessel.

Abstract: The present disclosure provides natural gas and petrochemical processing systems, including oxidative coupling of methane reactor systems that may integrate process inputs and outputs to cooperatively utilize different inputs and outputs in the production of higher hydrocarbons from natural gas and other hydrocarbon feedstocks. The present disclosure also provides apparatuses and methods for heat exchange, such as an apparatus that can perform boiling and steam super-heating in separate chambers in order to reach a target outlet temperature that is relatively constant as the apparatus becomes fouled. A system of the present disclosure may include an oxidative coupling of methane (OCM) subsystem that generates a product stream comprising compounds with two or more carbon atoms, and a dual compartment heat exchanger downstream of, and fluidically coupled to, the OCM subsystem.

Abstract: Catalyst systems and methods for making and using the same are described. A method includes selecting a catalyst blend using a blend polydispersity index (bPDI) map. The polydispersity map is generated by generating a number of polymers for at least two catalysts. Each polymer is generated at a different hydrogen to ethylene ratio. At least one catalyst generates a higher molecular weight polymer and another catalyst generates a lower molecular weight polymer. A molecular weight for each polymer is measured. The relationship between the molecular weight of the polymers generated by each of the catalysts and the ratio of hydrogen to ethylene is determined. A family of bPDI curves for polymers that would be made using a number of ratios of a blend of the at least two catalysts for each of a number of ratios of hydrogen to ethylene.

Abstract: A microreactor includes: a reaction passage to flow a fluid as a reaction object; and a medium passage provided in parallel with the reaction passage to flow a heat medium to exchange heat with the fluid in the reaction passage. A cross-sectional area of the medium passage adjacent to a location of the reaction passage where any of heat generation and heat absorption associated with a reaction of the fluid is relatively large is smaller than a cross-sectional area of the medium passage adjacent to a location of the reaction passage where any of the heat generation and the heat absorption associated with the reaction of the fluid is relatively small.

Abstract: The present invention provides methods and compositions for the chemical conversion of syngas to alcohols. The invention includes catalyst compositions, methods of making the catalysts, and methods of using the catalysts including techniques to maintain catalyst stability. Certain embodiments teach compositions for catalyzing the conversion of syngas into products comprising at least one C1-C4 alcohol, such as ethanol. These compositions generally include cobalt, molybdenum, and sulfur, and avoid metal carbides both initially and during reactor operation.

Abstract: Provided is a method of evaluating a resin capable of quantitatively evaluating a deterioration degree of the resin with high accuracy and ease. The method includes evaluating the resin based on a shift of a characteristic peak representing a deterioration degree of the resin, the peak being observed in thermal analysis of the resin by a temperature increase, to lower temperatures.

Abstract: A system for controlling an air/fuel ratio in an engine based on catalyst deactivation includes an NH3 detector disposed downstream from the three way catalyst, and a subsystem that compares measured values of NH3 concentration with a nominal value of NH3 concentration at rich operating conditions. A subsystem adjusts the air/fuel ratio based on the measured value of NH3 concentration and estimated CO concentration.

Abstract: The present disclosure provides identification techniques on platinum group metal (PGM) and zero platinum group metal (ZPGM) catalyst systems, in order to identify responsible materials for the formation of corrosion products, such as hexavalent chromium compounds. Identification analyses, such as X-ray diffraction analysis (XRD) and X-ray fluorescence (XRF) may be performed on various thermally treated PGM and ZPGM catalyst systems. Results of identification analyses may show that for both PGM and ZPGM catalysts, hexavalent chromium (Cr6+) may be formed during thermal aging at range of 600C to 900C. This may be due to the high concentration of chromium in substrate alloys. Therefore, occurrence of corrosion and production of hexavalent chromium may initiate from elements found in the substrate and not from elements within the PGM and ZPGM catalysts.

Abstract: A modular remote with touchscreen including a first member having a first sensor diposed on an anterior end and a first connection port disposed on a rear end; a second member having a touchscreen display disposed upon a top surface, a first connector disposed on a front side, a second sensor disposed on the front side, a second connection port disposed on a rear side; and a third member having a second connector disposed on a forward side; wherein the first connector interconnects with the first connection port and the second connector interconnects with alternately both the first connection port and the second connection port; whereby the first and third members interconnect to operatively communicate remotely with a plurality of household devices, and the second member separates from said first and third members to operatively communicate remotely with a plurality of household devices via interaction with a Graphic User Interface displayed by the touchscreen display.

Abstract: The present disclosure provides an identification process which may employ various identification techniques on Zero platinum group metal (ZPGM) catalyst systems, in order to identify responsible materials for the formation of corrosion material, such as hexavalent chromium compounds. Identification analysis, such as X-ray diffraction analysis (XRD), X-ray fluorescence (XRF), and X-ray Photoelectron Spectroscopy (XPS) may be performed on various thermally treated ZPGM catalyst systems, such as in bare substrate, substrate with one type of ZPGM in washcoat, a substrate with one type of ZPGM in overcoat and substrate combination of ZPGM metals in both washcoat and overcoat. Results of identification analysis may show that regardless of metal catalyst (for example Ag, Cu, Ce), hexavalent chromium (Cr6+) may be formed on aged catalysts systems, which may be due to the high concentration of chromium in substrate.

Abstract: The purpose of the present invention is to grasp the state in which hydrophilic groups of an electrolyte are distributed in a reaction layer for fuel cells. Nitric acid groups are bonded to hydrophilic groups (sulfonic acid groups) contained in a reaction layer for fuel cells, and metal ions capable of forming a nitrosyl complex with the nitric acid groups, e.g., ruthenium ions, are introduced into the reaction layer to dye the nitric acid groups bonded to the hydrophilic groups contained in the reaction layer. When the hydrophilic groups have agglomerated, the nitric acid groups bonded thereto also agglomerate. When said nitric acid groups are dyed with ruthenium, the ruthenium also agglomerates to make it possible to examine said nitric acid groups with an electron microscope.

Abstract: Methods and devices for directly measuring the degree of saturation or degree of deactivation of an adsorbent and/or catalytic bed are described herein. The devices contain an inlet, an outlet, a catalytic and/or adsorbent bed, and optionally a support bed for supporting the catalytic and/or adsorbent bed. The devices further contain one or more structures attached to the reactor that allow for insertion of one or more sensors into the reactor. The sensor is used to spectroscopically interrogate the adsorbent and/or catalyst in situ, providing real-time information regarding adsorbant saturation and/or catalyst deactivation. The devices and methods described herein can be used to determine the saturation degree of adsorbent materials or catalyst beds that are involved in gas-liquid and liquid-liquid heterogeneous systems, such as those used in scrubbing and extraction.

Abstract: In a method for operating an exhaust gas purifying device, with at least one catalyst for filtering exhaust gas and at least one lambda sensor arranged in the exhaust gas, an end of a time period assigned to a maximum or minimum of a delayed signal value supplied by the lambda sensor is determined in that a variable value tracks the signal value and, if the signal value falls short of or exceeds the variable value by a specific difference value, the end of the time period is determined. The end of a time period is corrected on the basis of the time constant of the delay.

Abstract: A method for recognizing sensor poisonings in portable gas-measuring devices with a test station having a main unit with a control and analysis unit and test modules connected with the main unit for data exchange with an connected device. The test station recognizes device model and/or gas sensor model of the connected device. The main unit has gas inlets for different test gases and there is a first gas feed line for sending test gas to the test modules and a second gas feed line for sending purging gas to the test modules and a gas drain line to return gas from the test modules to the main unit. The method includes detection of a first measured value and of a second measured value and determination of sensor poisoning on the basis of the two values. The test station control and analysis unit carries out the method.

Abstract: The present disclosure may include a method for preparing gas mixtures of use in testing catalysts, where the method may include using separate banks of mass flow controllers for mixing the gas composition to the desired composition and for controlling the flow of the gas composition through the heater. A separate bank may be used for controlling any suitable mix of reducing agents while another separate bank may be used for controlling any suitable mix of oxidizing gases.

Abstract: Disclosed herein is a method of separating variations in the mass flow of gas through a catalyst from the thermal load observed by the temperature control system in a test bench. The method may include separating the temperature control component from the mass flow control component.

Abstract: Devices contain dried reagents that may be reconstituted and used in the calibration and quality control of sensors. Methods of producing and using the devices are also disclosed.

Abstract: A method for determining a degree of aging of an oxidizing catalytic converter in an exhaust system of an internal combustion engine is provided. The method comprises generating a temporary increase in carbon monoxide levels in an exhaust gas stream, monitoring subsequent oxidizing action and determining a degree of aging of the oxidizing catalytic converter as a function of the measured oxidizing action. The method further comprises measuring a temperature rise during oxidation and correlating the aging of the converter to the speed of temperature rise.

Abstract: A process for determining ionic liquid catalyst deactivation including (a) collecting at least one sample of an ionic liquid catalyst; (b) hydrolyzing the at least one sample to provide at least one hydrolyzed sample; (c) titrating the at least one hydrolyzed sample with a basic reagent to determine a volume of the basic reagent necessary to neutralize a Lewis acid species of the ionic liquid catalyst; and (d) calculating the acid content of the at least one sample from the volume of basic reagent determined in step (c) is described. Processes incorporating such a process for determining ionic liquid catalyst deactivation are also described. These processes are an alkylation process, a process for controlling ionic liquid catalyst activity in a reaction producing by-product conjunct polymers, and a continuous process for maintaining the acid content of an ionic liquid catalyst at a target acid content in a reaction producing by-product conjunct polymers.

Abstract: Disclosed is a performance game, and more particularly is a method, an apparatus, and a recording medium for a performance game, which can provide various presentation effects with a simple presentation operation of a user.

Abstract: Methods and systems for controlling and/or diagnosing an emission control system of a vehicle having a first SCR region upstream of a second SCR region are provided herein. One exemplary method includes, indicating degradation based on a first SCR region performance during a first condition; and indicating degradation based on a second SCR region performance during a second condition, the first condition different than the second condition. In this way, different levels of degradation among different SCR regions may be used to indicate emissions levels have increased above a threshold value, for example.

Abstract: A sulfur breakthrough monitoring assembly for use in a fuel utilization system for detecting sulfur-containing compounds in desulfurized fuel, said monitoring assembly comprising: a heater for heating desulfurized fuel to a predetermined temperature, the predetermined temperature being between 450° C. and 600° C., a sulfur breakthrough detector adapted to receive heated fuel from the heater and including at least a reforming catalyst bed for reforming the heated fuel and a plurality of temperature sensors including a first temperature sensor for sensing temperature of the heated fuel before the fuel is conveyed through the reforming catalyst bed and a second temperature sensor for sensing temperature in the reforming catalyst bed, and a controller for determining whether concentration of the sulfur-containing compounds in the fuel exceeds a first predetermined concentration based on temperature outputs from the first and second temperature sensors.

Abstract: The inventive device serves for simultaneous supply of nonvolatile reactant liquid to a plurality of mixing points or to a plurality of reactors, the device comprising a reservoir vessel, a supply line and a splitter which divides the supply line into a group of downstream lines. Each individual downstream line is functionally connected to one mixing point or one reactor and each is equipped with a restrictor element, the restrictor elements and at least parts of the downstream lines being in contact with a sheath having a temperature control unit.

Abstract: A method for estimating a particulate content in a slurry of the present invention is a method for estimating a content of particulates having a predetermined particle size or less in a slurry with solid particles dispersed in hydrocarbons including a wax, the method including, based on a correlation between a visible light transmittance and a content of solid particles having the predetermined particle size or less at a temperature at which hydrocarbons including a wax are liquefied when the solid particles having the predetermined particle size or less are dispersed in the hydrocarbons, estimating a content of particulates having the predetermined particle size or less in the slurry from a visible light transmittance of a supernatant part when the slurry is left to stand at the temperature.

Abstract: A process for determining ionic liquid catalyst deactivation including (a) collecting at least one sample of an ionic liquid catalyst; (b) hydrolyzing the at least one sample to provide at least one hydrolyzed sample; (c) titrating the at least one hydrolyzed sample with a basic reagent to determine a volume of the basic reagent necessary to neutralize a Lewis acid species of the ionic liquid catalyst; and (d) calculating the acid content of the at least one sample from the volume of basic reagent determined in step (c) is described. Processes incorporating such a process for determining ionic liquid catalyst deactivation are also described. These processes are an alkylation process, a process for controlling ionic liquid catalyst activity in a reaction producing by-product conjunct polymers, and a continuous process for maintaining the acid content of an ionic liquid catalyst at a target acid content in a reaction producing by-product conjunct polymers.

Abstract: The present invention provides methods and compositions for the chemical conversion of syngas to alcohols. The invention includes catalyst compositions, methods of making the catalysts, and methods of using the catalysts including techniques to maintain catalyst stability. Certain embodiments teach compositions for catalyzing the conversion of syngas into products comprising at least one C1-C4 alcohol, such as ethanol. These compositions generally include cobalt, molybdenum, and sulfur, and avoid metal carbides both initially and during reactor operation.

Abstract: A method and an arrangement for dynamic breakthrough detection is proposed. The arrangement comprises at least a transfer element, at least a memory unit in which sensor characteristic curves, at least a controller and an evaluation logic are stored.

Abstract: The present invention relates to a method for predicting the efficiency of a TiO2 photocatalyst in a light-induced reaction.

Abstract: Sensors for sensing/measuring one or more analytes in a chemical environment. Each sensor is based on a semiconductor structure having an interfacial region containing a two-dimensional electron gas (2DEG). A catalyst reactive to the analyte(s) is in contact with the semiconductor structure. Particles stripped from the analyte(s) by the catalyst passivate the surface of the semiconductor structure at the interface between the catalyst and the structure, thereby causing the charge density in the 2DEG proximate the catalyst to change. When this basic structure is incorporated into an electronic device, such as a high-electron-mobility transistor (HEMT) or a Schottky diode, the change in charge density manifests into a change in an electrical response of the device. For example, in an HEMT, the change in charge density manifests as a change in current through the transistor, and, in a Schottky diode, the change in charge density manifests as a change in capacitance.

Abstract: The present invention relates to a catalysis apparatus for testing catalysts with variable process pressure adjustment over a pressure range from 0.01 millibar to 300 bar. The apparatus preferably has a plurality of reaction chambers (101, 102, . . . ) arranged in parallel, the reaction chamber outlet-side lines (211, 212, . . . ) of which are divided into two groups of sub-lines. One group of main lines (411, 412, . . . ) is operatively connected to a regulating valve (61), which is common to all of the main lines, and to an exhaust-air line (62), and the second group of secondary lines (311, 312, 313, . . . ) and switching valves (321, 322, . . . ) is operatively connected to an analysis unit (34). It is preferable for reaction chamber outlet-side lines (201, 202, . . . ) to be equipped in each case with a separate line for regulating fluid supply (211, 212, . . . ). In a preferred embodiment, the connecting points of the reaction chamber outlet-side lines (201, 202, . . .

Abstract: In an input device, a controller for controlling an input portion and acquiring data is connected to a bus. The bus can be connected with an external expansion device via an expansion connector. The connection of the bus from the expansion connector to the controller is switched on and off by a switcher. Data acquired from a sensor having a function equivalent to that of the external expansion device is transmitted to the controller via the bus by a sensor controller which is connected to each of a side of the controller and a side of the expansion connector of the bus without interposing the switcher. The sensor controller switches the connection of the switcher off when an access to itself is made from the controller.

Abstract: The present invention provides a method for selecting an improved catalyst composition comprising a crystalline molecular sieve material having a structure and properties whereby the catalyst composition has at least one active catalytic site with a Mono Alkylation Selectivity Factor (MASF) greater than or equal to 0 kcal/mol±0.5 kcal/mol, and optionally further at least one active catalytic site with an Olefin Oligomerization Suppression Factor (OOSF) greater than or equal to 5 kcal/mol±0.5 kcal/mol. Further, there is provided an improved process for conversion of hydrocarbon feedstock in the presence of said selected catalyst composition.

Abstract: A video game controller with a position sensor and a proximity sensor provides user input signals for use in determining game states. The video game controller can have a board or deck like surface similar to that of a skateboard, and the proximity sensor can be used to determine if a grab of the board has been attempted. A video game associated with the video game controller can provide a skateboard or other game in which a skateboard and skateboarding character are responsive to a game player's manipulation of the video game controller.

Abstract: Various systems, game controllers, and methods for simulating various objects such as weapons are provided. For example, a game controller may include a trigger, a processor within the body that receives a trigger signal when the trigger is activated by the user. The processor may communicate with a computer running a software program such as a gaming application, and an actuator coupled to the trigger, the actuator configured to output a haptic effect to the trigger in response to receiving a control signal from the processor. The game controller may simulate a gun and generate a recoil effect. In some embodiments, the recoil effect may be generated by impacting a moving mass from a discharge end of the gun to a handle end of the gun. In some embodiments, the recoil effect may be generated by using a body part of a user as a tether.

Abstract: Process for evaluating the effect of a refinery feedstock on a refinery process by (i) providing a refinery feedstock (ii) treating the refinery feedstock to produce a plurality of fractions each representative of a feedstock for the refinery process, the plurality of fractions having at least two fractions with different properties; (iii) treating each of the plurality of fractions under experimental conditions representative of those in the refinery process, the treatments being carried out in an essentially parallel manner; and (iv) determining one or more performance criteria for each fraction for the refinery process by analyzing the respective product streams produced from each fraction at least partially in parallel.