Abstract:
A baseball bat which includes one or more colored bands with transferrable colored pigments in or adjacent to the hitting zone to assist a batter in determining where a ball is hit on the hitting zone of the bat. The colored bands on the bat have a color pigment that will mark the ball when hit. The marked ball will provide an indication of where the bat impacted the ball. This information can be used to better train the players in hitting the balls.
Abstract:
A fiberoptic assembly for optical spectroscopic analysis of a sample. In a preferred embodiment, the assembly is well-suited for use inside the working channel of an endoscope and comprises a tubular outer jacket and a tubular inner jacket, the inner jacket being coaxial with and positioned inside the outer jacket. The open front end of the inner jacket is spaced rearwardly a short distance relative to the open front end of the outer jacket. The outer jacket has an outer diameter of approximately 2.2 mm. The assembly also includes a plug made of fused silica. The plug has a front cylindrical portion of comparatively large cross-sectional diameter and a rear cylindrical portion of comparatively small cross-sectional diameter. The front portion is mounted within the outer jacket by a friction-fit and extends longitudinally from the open front end thereof to the open front end of the inner jacket. The rear portion of the plug is mounted within the inner jacket by a friction-fit and extends rearwardly from its open front end for a short distance. A narrow-band filter in the form of a dielectric-coating is formed on the rear end of the rear portion of the plug. The assembly also includes an illumination fiber centered within the inner jacket and spaced rearwardly a short distance from the narrow-band filter. The output end of the illumination filter is shaped to collimate light emergent therefrom. The assembly additionally comprises a plurality of light collection fibers, which fibers are disposed within the outer tubular jacket and are spaced about the outside of the inner tubular jacket.
Abstract:
A method for imaging objects in highly scattering turbid media. According to one embodiment of the invention, the method involves using a plurality of intersecting source/detectors sets and time-resolving equipment to generate a plurality of time-resolved intensity curves for the diffusive component of light emergent from the medium. For each of the curves, the intensities at a plurality of times are then inputted into the following inverse reconstruction algorithm to form an image of the medium: X.sup.(k+1).spsp.T =�Y.sup.T W+X.sup.(k).spsp.T .LAMBDA.!�W.sup.T W+.LAMBDA.!.sup.-1 wherein W is a matrix relating output at detector position r.sub.d, at time t, to source at position r.sub.s, .LAMBDA. is a regularization matrix, chosen for convenience to be diagonal, but selected in a way related to the ratio of the noise, to fluctuations in the absorption (or diffusion) X.sub.j that we are trying to determine: .LAMBDA..sub.ij =.lambda..sub.j .delta..sub.ij with .lambda..sub.j = / Here Y is the data collected at the detectors, and X.sup.k is the kth iterate toward the desired absoption information.
Abstract:
A method and apparatus for evaluating the composition of an oil sample. The method and apparatus are premised on the discovery that spectral differences can be observed in the luminescence, excitation, light scattering and absorption spectra in the near UV, visible and near IR regions for various crude oil components, such as asphaltenes, deasphalted crude oil and organic solid residues. Accordingly, in one preferred embodiment the method comprises illuminating an oil sample with light of a suitable excitation wavelength, measuring the resultant fluorescence therefrom and comparing the resultant fluorescence to appropriate standards derived from known components of crude oil.
Abstract:
A method and device for detecting fluorescent biological molecules and/or microorganisms containing said fluorescent biological molecules within a given area or space. The method comprises illuminating an area or space with light of a suitable wavelength to excite the fluorescent biological molecules and then measuring the resultant fluorescent light from the illuminated area or space at a wavelength indicative of fluorescence of the fluorescent biological molecules. The invention can also be used to detect changes in the levels of such biological molecules and/or microorganisms within a given area or space by illuminating the area or space at two different times, measuring the resultant fluorescence after each illumination and comparing the respective fluorescence measurements. The present invention is also directed to a hand-held device for in vivo inspection of desired areas or spaces.
Abstract:
A system for imaging an object in or behind a highly scattering medium includes a laser for illuminating the highly scattering medium with a beam of light. The light emerging from the highly scattering medium consists of a ballistic component, a snake-like component and a diffuse component. A 4F Fourier imaging system with a Kerr gate located at 2F is used to form a time-space gated image of the emerging light, the time-space gated image consisting primarily of the ballistic component and the snake-like component.
Abstract:
A method for determining if tissue is malignant as opposed to non-malignant (i.e., benign tumor tissue, benign tissue, or normal tissue), In one embodiment, the method comprises irradiating a human breast tissue sample with light at a wavelength of about 310 nm and measuring the time-resolved fluorescence emitted therefrom at about 340 nm. The time-resolved fluorescence profile is then compared to similar profiles obtained from known malignant and non-malignant human breast tissues. By fitting the profiles to the formula I(t)=A.sub.1 e(-t/.tau..sub.1)+A.sub.2 e(-t/.tau..sub.2) one can quantify the differences between tissues of various conditions. For example, non-malignant human breast tissues exhibit a slow component (.tau..sub.2) which is less than 1.6 ns whereas malignant human breast tissues exhibit a slow component (.tau..sub.2) which is greater than 1.6 ns. In addition, non-malignant human breast tissues exhibit a ratio of fast to slow amplitudes (A.sub.1 /A.sub.2) which is greater than 0.85 whereas malignant human breast tissues exhibit a ratio of fast to slow amplitudes (A.sub.1 /A.sub.2) which is less than 0.6. This technique can be used with different excitation and/or emission wavelengths, and can be applied to the detection of malignancies (or other abnormal states) in tissues other than human breast tissue.
Abstract:
A multiple-stage optical Kerr gate system for gating a probe pulse of light. In a first embodiment, the system includes at least two optical Kerr gates, each Kerr gate including a polarizer, an optical Kerr cell actuable by a pump pulse, and an analyzer. In a second embodiment, at least one of the Kerr cells may be eliminated by arranging the respective sets of polarizers and analyzers so that they share a common Kerr cell. Gated pulses obtained using the present system typically have a signal to noise ratio that is at least 500 times better than that for gated pulses obtained using a single optical Kerr gate system. The system of the present invention may also include means for causing the pump pulse to arrive at the second Kerr cell (in the case of the first embodiment) or at a single Kerr cell a second time (in the case of the second embodiment) non-synchronously with the arrival of the probe pulse thereat. In this manner, gated pulses may be obtained that are much shorter in duration than pulses gated with a single optical Kerr gate system.
Abstract:
An apparatus for producing a 3-dimensional image of semi-transparent object or of a opaque object in a semi-transparent media includes a picosecond or a femtosecond laser, a streak camera, a coherent fiber bundle, a video camera and a computer. The apparatus provides a unique nondestructive and non-invasive diagnostic way for detecting, for example, objects hidden in semi-opaque media. The laser is used to produce an ultrashort light pulse. The coherent fiber bundle is used to convert the 2-dim spatial image that is produced (i.e. scattered or fluorescence light from a 3-dim object illuminated with the ultrashort laser pulse) into a 1-dim line image which is fed into the input slit of the streak camera and then time resolved by the streak camera. The video camera is used to record the 2-dim output (1-dim from input image and 1-dim of the streak time) from the streak camera. The output of the video camera is fed into the computer. In the computer 2-dim data elements are reconstructed into a 3-dim image and then displayed on a monitor. This apparatus essentially converts a streak camera into the equivalent of a framing camera with continuous time imaging capability.
Abstract:
The quality of image of an object hidden inside a highly scattering semi-opaque disordered medium is improved by using space gate imaging or time gate imaging or space time gate imaging. In space gate imaging, a small segment of the object is illuminated at a time. The scattered light is passed through a spatial noise filter. On the image plane, an aperture is open at the position of the image segment which correspond to the segment of the illuminated object. A full image is obtained by scanning the object segment by segment and simultaneously recording the signal at the corresponding image segment. In time gate imaging, the unscattered (i.e. ballistic) portion of the pulse which contains the information of the image is temporally separated from the other (i.e. scattered) portions which contains the noise using a ultrafast laser pulse and temporal gating devices. The technique is in space-time gate imaging, the two techniques are combined to produce an image with a much higher signal to noise ratio. The time separation between the ballistic and scattered light may be increased by increasing thickness of random medium or by introducing small scatters into the random medium so as to make the medium more random. The signal to noise ratio can also be increased by making the random medium less random (so that there will be less scattered light). In addition, the signal to noise ratio can be increased by introducing an absorbing dye into the medium or by using a wavelength for the light which is in the absorption spectrum of the random medium or by making the medium more ordered (i.e. less random) or by using a pair of parallel polarizers.