Author: claimsbot

1. A method comprising:
displaying, by a computing device, a plurality of components of a graphical user interface, wherein each of the plurality of components displays one or more members of at least one dimensional level of a database having a plurality of dimensions, and wherein each dimension of the plurality of dimensions includes one or more dimensional levels;
determining, by the computing device, a first dimensional level of a first dimension of the plurality of dimensions having one or more members displayed in two or more of the plurality of components; and
displaying, by the computing device, a control element including an indication of the dimensional level having the one or more members displayed in each of the two or more components.
2. The method of claim 1, further comprising:
receiving, by the computing device, a selection of a member of a second dimensional level of the first dimension using the control element; and
updating, by the computing device, each of the two or more components to cause the two or more components to display one or more members of a child dimensional level of the first dimensional level of the selected member.
3. The method of claim 2, wherein the one or more members of the child dimensional level include the one or more members of the intersection of the selected member of the first dimensional level and the members of the child dimensional level.
4. The method of claim 1, further comprising:
receiving, by the computing device, a selection of an indication of a second dimensional level of the first dimension using the control element; and
updating, by the computing device, each of the two or more components to cause the two or more components to display one or more members of a second dimensional level indicated by the selection.
5. The method of claim 4, wherein the selection of the indication of the second dimensional level includes a selection of the indication of the intersection of the second dimensional level with a member of a parent dimensional level of the second dimensional level.
6. The method of claim 1, further comprising:
receiving, by the computing device, a selection of a second dimension of the database; and
updating, by the computing device, the two or more components to cause the two or more components to display one or more members of a dimensional level of the second dimension.
7. The method of claim 1, further comprising:
determining, by the computing device, a second dimensional level of a second dimension having one or more members displayed in two or more of the plurality of components; and
displaying a control element including an indication of the second dimensional level of the second dimension having one or more members displayed in two or more of the plurality of components.
8. The method of claim 7, further comprising:
receiving, by the computing device, a selection of a member of a third dimensional level of the second dimension using the control element; and
updating, by the computing device, each of the two or more components to cause the two or more components to display one or more members of a child dimensional level of the third dimensional level of the selected member.
9. The method of claim 7, further comprising:
receiving, by the computing device, a selection of an indication of a fourth dimensional level of the second dimension using the control element; and
updating, by the computing device, each of the two or more components to cause the two or more components to display one or more members of the fourth dimensional level indicated by the selection.

The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.

1. A process for the extraction of uranium compounds from wet-process phosphoric acid (WPA), the process comprising:
lowering iron content of WPA by precipitating iron to produce a lowered iron WPA;
reducing valency of any remaining iron in the lowered iron WPA to produce a reduced iron valency WPA; and
extracting uranium compounds from the reduced iron valency WPA using an ion exchange process comprising contacting the reduced iron valency WPA with an ion exchange resin and eluting the ion exchange resin.
2. The process of claim 1, wherein the ion exchange process comprises passing the WPA through a multi-stage chelating ion exchange column system and eluting the ion exchange column system.
3. The method of claim 1, wherein lowering iron content of WPA to produce a lowered iron WPA comprises precipitating the iron as iron ammonium phosphate.
4. A process for the extraction of uranium compounds from wet-process phosphoric acid (WPA), the process comprising:
lowering the iron content of WPA to produce a lowered iron WPA;
reducing the valency of iron in the lowered iron WPA to produce a reduced iron valency WPA; and
extracting uranium compounds from the reduced iron valency WPA,
wherein lowering the iron content of the WPA comprises precipitating the iron as an iron ammonium phosphate compound;
wherein reducing the valency of iron in the WPA comprises reducing ferric iron to ferrous iron by contacting the WPA with one or more substances selected from the group consisting of: a ferro-phosphorous compound, a ferro-silicon compound, and metallic iron, and
wherein extracting uranium compounds comprises an ion exchange process comprising passing the WPA through a multi-stage chelating ion exchange column system and eluting the ion exchange column system.
5. A process for the extraction of uranium compounds from wet-process phosphoric acid (WPA), the process comprising:
lowering iron content of WPA by precipitating iron to produce a lowered iron content WPA;
adding a reducing agent to the lowered iron content WPA to reduce the valency of any remaining iron in the lowered iron content WPA and produce a reduced iron valency WPA; and
extracting uranium compounds dissolved in the reduced iron valency WPA using an ion exchange process by contacting the reduced iron valency WPA with an ion exchange resin and eluting the ion exchange resin.
6. The method of claim 5, wherein lowering iron content of WPA to produce a lowered iron WPA comprises precipitating the iron as iron ammonium phosphate.

1. A system control for a diagnostic imaging apparatus comprising:
a user interface adapted to permit a user to enter data specific to a given scan;
a scan subject monitor configured to monitor at least one dynamic scan subject parameter;
a scan protocol module connected to receive data entered by the user on the user interface and the at least one dynamic scan subject parameter and programmed to prescribe a scan protocol to optimize contrast enhancement;
a contrast delivery device controlled by the scan protocol module to cause a contrast agent to be delivered to a scan subject in accordance with the prescribed scan protocol; and
an acquisition control configured to coordinate commencement of the given scan in accordance with the scan protocol.
2. The system control of claim 1 wherein the data specific to the given scan includes at least one of a static scan subject parameter and a scan type.
3. The system control of claim 1 wherein the scan protocol includes a contrast agent delivery protocol.
4. The system control of claim 3 wherein the scan protocol includes a number of contrast agent delivery protocols corresponding to a number of injection phases of a diagnostic imaging scan.
5. The system control of claim 1 wherein the contrast delivery device includes at least one of an automated contrast injection device to inject the contrast agent and an indicator to inform an operator when to administer the contrast agent.
6. The system control of claim 1 wherein the scan protocol module is configured to adapt the prescribed scan protocol in real time in accordance with changes in the at least one dynamic scan subject parameter.
7. The system control of claim 1 wherein the scan protocol module is configured to adapt the prescribed scan protocol in real time in accordance with a real time contrast enhancement value for a region of interest, calculated from scan data acquired therefrom.
8. The system control of claim 1 wherein the scan subject monitor is configured to track a bolus in the scan subject, as an indicator of contrast agent flow.
9. The system control of claim 8 wherein the scan protocol module is configured to receive bolus tracking data from the scan subject monitor and trigger the acquisition control in real-time to begin the given scan, based on the bolus tracking data.
10. A method for contrast-enhanced diagnostic imaging comprising:
estimating, for a given scan subject, a post-delivery time for a desired contrast agent enhancement value, based on a number of subject parameters, a number of contrast agent parameters, and a number of scan parameters;
administering the contrast agent;
timing at least a portion of an imaging scan sequence to coincide with the post-delivery desired contrast enhancement time of the contrast agent;
adapting at least one of the number of contrast agent parameters and the number of scan parameters during the scan sequence to maintain the timing of the desired contrast enhancement and the portion of the imaging scan sequence; and
reconstructing an image of the scan subject based at least on scan data acquired during the post-delivery desired contrast enhancement time.
11. The method of claim 10 wherein the number of subject parameters include static subject parameters and dynamic subject parameters.
12. The method of claim 11 wherein the number of static subject parameters include subject weight, gender, age, height, and body mass index, and the number of dynamic subject parameters include heart rate, blood pressure, respiratory rate, and timing bolus data.
13. The method of claim 10 wherein the number of contrast agent parameters include contrast agent type, bolus type, number of injection phases, contrast agent volume, contrast agent flow rate, injection duration, and contrast enhancement duration.
14. The method of claim 10 wherein the number of scan parameters include a scan dosage, a scan speed, a scan resolution, and a field of view.
15. The method of claim 10 further comprising performing a timing bolus scan prior to the imaging scan sequence.
16. The method of claim 14 further comprising determining a time density curve for a region of interest from the timing bolus scan.
17. The method of claim 10 further comprising performing a real-time bolus tracking after injecting the contrast agent.
18. The method of claim 17 further comprising automatically triggering the imaging scan sequence to coincide with the peak contrast enhancement time, based on the real-time bolus tracking.
19. The method of claim 10 wherein adapting at least one of the number of contrast agent parameters and the number of scan parameters during the scan sequence includes monitoring a real-time contrast enhancement calculated from image data and monitoring dynamic scan subject parameters.
20. A computer-readable storage medium having a set of instructions stored thereon which, when executed by the computer, causes the computer to:
prompt a user to enter patient-specific information for a given scan patient;
prompt a user to select a scan type;
receive bolus tracking data for the given patient; and
provide an individualized scan protocol defining a contrast agent delivery and scan sequence timing, based upon the patient-specific information, the scan type, and the bolus tracking data.
21. The computer-readable storage medium of claim 20 wherein the set of instructions further causes the computer to receive the bolus tracking data in real-time.
22. The computer-readable storage medium of claim 21 wherein the set of instructions further causes the computer to automatically trigger commencement of a scan sequence based upon the real-time bolus tracking data.
23. The computer-readable storage medium of claim 20 wherein the set of instructions further causes the computer to display default contrast agent parameters to a user after entry of the patient-specific information, selection of the scan type, and receipt of the bolus tracking data.
24. The computer-readable storage medium of claim 23 wherein the default contrast agent parameters include a post-delivery peak contrast enhancement period.
25. The computer-readable storage medium of claim 23 wherein the instructions further cause the computer to display the contrast agent parameters and a number of scan parameters to the user and prompt the user to confirm the parameters prior to contrast delivery and scan commencement.
26. The computer-readable storage medium of claim 18 wherein the instructions further cause the computer to control a contrast pump to automatically deliver a contrast agent to the patient in accordance with the protocol.
27. The computer-readable storage medium of claim 20 wherein the instructions further cause the computer to calculate a real time contrast enhancement value for a region of interested based upon at least one of image data acquired in a scan and the dynamic patient-information.
28. The computer readable storage medium of claim 27 wherein the instructions further cause the computer to adapt at least one of the scan parameters and contrast agent parameters in real time during the scan such that a desired portion of the scan substantially coincides with a desired contrast enhancement value.
29. The computer readable storage medium of claim 28 wherein the instructions further cause the computer to adjust x-ray dosage, pitch, or gantry rotation in a CT scan such that a period of maximum dosage of the CT scan substantially coincides with a peak contrast enhancement value.
30. The computer readable storage medium of claim 28 wherein the instructions further cause the computer to adjust contrast agent flow rate, pressure, or volume to achieve a maximum contrast enhancement value during a period of maximum dosage of a CT scan.

The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.

1. A barrier, installed in the sewage pipe and intended to prevent the penetration of rats, that comprises a main body shaped like a short hollow sleeve, a main obstructing plate, a secondary obstructing plate, a first locking tongue, and a second locking tongue; whereby the sleeve is shaped like a short hollow pipe with a flat top part; and whereby the main obstructing plate is shaped like an ellipse whose upper edge is truncated, forming a straight line, and which has a hole at the bottom beneath which are two protruding pins: A top pin and a bottom pin; and whereby the secondary obstructing plate is also shaped like an ellipse with a truncated upper edge, forming a straight line, and has a protruding pin near its bottom edge; and whereby the first and second locking tongues have the general shape of a rectangle; and whereby the main obstructing plate, the secondary obstructing plate, and the locking tongues are all attached to the flat top of the sleeve, from the inside, using hinges.
2. The barrier, mentioned in claim No. 1, whereby it includes only one locking tongue.