Micromeritics Instrument Corporation

Micromeritics

Micromeritics Instrument Co.

Ronnie W Camp

Clyde Orr, Jr

Dean M Ball

Warren P Hendrix

William B Conklin

Graham R Killip

Cyde Orr, Jr

Kathryn H Gibson

A compaction device for determining envelope and bulk densities of sample materials. The device uses a rotating sample cylinder and a plunger positioned within the cylinder. The force on the plunger is measured as the plunger advances in the cylinder. The position of the plunger at which a predetermined level of force is applied thereto is determined. Envelope density is determined from the difference in the advance of the plunger when the cylinder is partially filled with a dry flowing medium and when a sample material such as a rigid object is added into the medium. Bulk density is determined from the difference in the advance of the plunger when the cylinder is empty and when the cylinder contains a sample material such as a powder.

Method and apparatus for measuring envelope and bulk densities

An apparatus and method for measuring the volume and calculating the envelope density of an object of known weight. The apparatus has a hollow sample cylinder of known interior diameter mounted to a motor for rotation about its horizontal axis. A dry flowing medium is placed in the sample cylinder and a plunger is removably positioned therein. The plunger is mounted to another drive motor for axial movement within the sample cylinder to compact the dry flowing medium. A load cell connected to the plunger measures the force on the plunger as it advances in the sample cylinder. Control means responsive to the load cell determines the position of the plunger in the sample cylinder at which a known force is exerted on the plunger. The control means also calculates the volume of the dry flowing medium in the sample cylinder both with and without the object positioned therein and divides the difference in the volumes into the weight of the object.

Method and apparatus for measuring envelope density

An apparatus and method are disclosed for obtaining adsorption data to be used for surface area and pore volume analysis. The apparatus and method utilize the differential pressures between a pair of dosing systems to indicate the amount of gas adsorbed by a sample. The system doses a sample chamber and a null chamber from essentially equal volumes of gas, and causes the chambers to be dosed such that any pressure difference between them, caused by adsorption, is eliminated. The resulting differential pressure between the essentially equal volumes of gas then indicates the amount of gas adsorbed by the sample. The system may be operated to dose in equilibrated increments or in a scanning mode in which adsorbate gas is continuously leaked into the sample chamber. A feedback circuit then controls dosing into the null chamber to eliminate the pressure difference caused by adsorption onto the sample surface. A differential pressure transducer connecting the volumes from which the gas is released then indicates the amount of gas adsorbed.

Dynamically balanced, differential gas adsorption appartaus

A gas comparison pycnometer is disclosed which provides a method and apparatus for determining and checking the accuracy of the volume of a solid substance. The pycnometer is also outfitted with a unique cap assembly which fixes the volume in the pycnometer's sample chamber from run to run. The pycnometer also employs a series of purges with a suitable gas to carry unwanted moisture and vapors out of the system. This pycnometer solves many problems in the prior art by quickly and accurately determining the volume of a solid substance.

Gas comparison pycnometer

The invention provides improvements in a system for carrying out volumetric sorption analysis of porous materials. According to one aspect of the invention, the saturation pressure of the adsorbate gas is measured after dosing of the sample during an actual run has brought the adsorbate gas to a saturation condition above the sample, and this measured saturation pressure is then used by the system to determine the relative pressures at which data will be taken during desorption. In accordance with another aspect of the invention, the system automatically adds extra adsorbate gas to the dosing manifold until the analysis proceeds beyond a selected relative pressure, so that far fewer doses are required to reach initial target relative pressures in the case of materials which adsorb large amounts of gas at low relative pressures.

System for dosing and determining saturation pressure in a volumetric

An automated device for warming and cooling a sample is disclosed, and is particularly useful in connection with a flowing gas surface area analyzer. The device is capable of directing a flow of room temperature air onto a sample chamber after the chamber is removed from a coolant, thus rapidly warming the sample up to, but not exceeding, room temperature. In the disclosed embodiment, a Dewar flask containing coolant is mounted on an elevator platform. The flask is mechanically raised or lowered so as to immerse the sample chamber, located above the flask, in the coolant. A fan directs a flow of air onto the sample after the flask is lowered away from the sample chamber. A logic controller, connected to a timer, operates and regulates the cooling and warming process. The elevator assembly, fan and controller are disposed within a housing. The sample chamber is connected to gas input and output tubes, which are monitored by a detector for the composition of gas passing through the tubes. A method is also disclosed for analyzing the surface area of a sample using the device.

Sample warming device for surface area analyzer

An automatic sample feeder system for handling suspended samples is disclosed, and is particularly useful in connection with a sedimentation particle size analyzer. The system is capable of dispersing a particulate sample into suspension without preliminary sample preparation, maintaining a sample in suspension at the time of delivery of the sample to an analyzer, consistently delivering an acceptable concentration of a suspended sample, and cleaning and flushing its components between samples to avoid contamination. In the disclosed embodiment, sample beakers are arrayed on a rotatable tray, and a sample preparation and delivery assembly consisting of an ultrasonic probe, a stirrer blade, and a dip tube are indexed into position over the beakers in a preprogrammed sequence, and lowered into the beaker for preparation and withdrawal of the sample. The components are rinsed by directing clear liquid back through the dip tube onto the rotating stirrer blade, scattering the liquid.

Automatic sample feeder for suspended samples

An apparatus for maintaining a constant temperature within a vessel immersed in a liquid by surrounding a portion of the vessel, extending above the surface of the liquid, with a wick. The wick conducts liquid up to a predetermined point on the vessel and maintains the liquid at that point, regardless of changes in the level of the liquid due to evaporation. The wick is encased within a layer of heat insulating or heat conducting material to further aid in maintaining a constant temperature within the vessel. A second embodiment, including alternating layers of heat conducting and heat insulating material, is disclosed for increased temperature control. The disclosed apparatus is particularly useful for maintaining a constant temperature within a vessel attached to a scientific instrument, such as a pore volume and surface area analyzer.

Temperature controlling apparatus for use with pore volume and surface

Sample introduction apparatus useful in liquid chromatography and including a valve body having at least one fluid passage of precisely defined volume to receive a sample material and having another fluid passage delivering carrier liquid to a liquid chromatograph. The valve body can be manipulated to place the precisely defined volume in the chromatograph fluid circuit, so that the sample contained within the volume is positively displaced into the chromatograph.

Liquid chromatography sample measuring and introducing apparatus

Apparatus used in the field of liquid chromatography. There is disclosed pump apparatus for continuously delivering a flow of carrier liquid either at a constant rate of flow or at a constant pressure. The pump apparatus includes a pair of differential-piston pressure intensifiers which are sequentially operated so that the high-pressure sides of the pressure intensifiers sequentially supply carrier liquid to the chromatograph column. Each pressure intensifier is sequentially operated by a constant-rate of flow application of hydraulic liquid, with essentially pulseless operating transition between pressure intensifiers occurring during constant-pressure application of hydraulic liquid to both of the pressure intensifiers at a pressure measured during previous constant-volume hydraulic operation. An embodiment of the pump apparatus pumps plural carrier liquids in desired fixed or variable proportions. There is also disclosed sample introduction apparatus including a valve body having at least one fluid passage of precisely defined volume to receive a sample material and having another fluid passage delivering carrier liquid to a liquid chromatograph. The valve body can be manipulated to place the precisely defined volume in the chromatograph fluid circuit, so that the sample contained within the volume is positively displaced into the chromatograph. Chromatograph recycling apparatus is also disclosed which permits a selected sample portion to be retained after passing through a chromatograph column, and to be subsequently re-introduced into the column for further analysis. Apparatus is also disclosed for intermixing plural liquids flowing in a conduit. Improved detector apparatus for use with a chromatograph is also disclosed.

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Duluth, GA, United States of America

Ronnie W Camp