Microscopes TRIZ Cases

An immersion objective integrates a detachable fluid tank, pump, and control electronics directly onto the objective body.

Deflecting element redirects optical path to suppress vignetting during focal position adjustment in multi-detector scanning microscopes.

Three-group segmented immersion microscope objective lens achieves long working distance for thick sample observation while correcting chromatic aberrations.

An aperture stop near the rear focal plane maintains telecentricity across a 0.5 to 30 power range without increasing device size.

An information processing device analyzes entire images to detect observation targets and controls partial image acquisition order based on detection results.

Multiple time-scale sliding temporal filters separate overlapping emitter fluorescence signals based on distinct blinking patterns.

A microscope objective uses cemented lens groups to reduce production costs while correcting spherical aberration, coma, astigmatism, and chromatic aberration.

A fluorescence microscope apparatus uses a spatial light modulation element to create uniform illumination patterns across the specimen surface.

A spinning disk with pinholes rejects afocal light from the human retina.

Segmented lens groups adjust dynamically to provide wide field coverage and reduced distortion without vignetting on standard sensors.

A magnified observation apparatus adjusts focus during field of view changes using in-focus degree feature quantities.

Imaging the distal end of a multimode fiber onto a sample plane provides uniform radiant intensity, resolving single-mode transmission inefficiencies.

A conjugate lens directs incident light beams to a focal region and reflects them back for detection.

Angled illumination of a geometric reference structure enables precise focusing on structured surfaces without adding optical complexity.

Varying acoustic frequency slopes eliminates switching times and spot spreading, enabling continuous measurement with maintained integrity.

A scanning apparatus uses a tunable laser and displacement sensor to map specimen surfaces.

Movable prisms adjust optical path length in a variable image splitter, resolving z-direction localization errors and focus shifts during multi-plane imaging.

Voltage-controlled diffusers merge flood illumination with dot projection, reducing system size and complexity.

A polarization beam splitter directs incident light into two liquid crystal regions for independent phase modulation.

A beam expanding planar waveguide reduces beam splitter size and light waste while maintaining compact device dimensions.

A phase mask generates a light distribution with a localized radiation minimum on the detector plane to improve molecular localization precision.

An illumination controller rotates annular light emitting units at regular intervals to automate oblique specimen observation.

A variable focal length lens imaging system uses a sensor device to detect surface level variations and adjusts the object position in the focus direction.

A spring-loaded crash arm assembly enables rapid slide pickup and movement in automated imaging systems.

Segmented optical and digital imaging paths reduce radiation exposure while maintaining natural visual fidelity.

Segmented finger hooks on arm portions resolve weight and collision risks.

A movable stop arrangement merges partial image beams into a resultant beam, enabling one-handed operation without motorized complexity.

A multi-spectral structured illumination microscope employs an array mask and dispersion element to parallelize excitation across multiple wavelengths.

Observation system calculates focus position using spatial frequency analysis to resolve ambiguity from multiple contrast peaks in phase objects.

A wide-field microscope illumination system shifts the beam entry point across the objective lens aperture to protect optical components.

Segmenting a single DMD into separate illumination and detection zones prevents camera saturation from back-reflections while maintaining optical alignment.

A microscope system records images at varied focal depths to detect platelets through characteristic optical patterns.

Segmented reflective groups eliminate chromatic aberrations across broadband wavelengths without conical passage apertures.

A digital imaging system scans stained slides at high resolution to identify pathogens using machine learning classifiers.

A drive controller uses a tracking delayer to stabilize frequency changes in liquid lens systems.

An aperture pattern turret generates annular illumination lights with varying radii to compensate for phase shifts and interference from cover glass interfaces.

An all-focus image combines weighted microscopy slices into a single view to simplify spatial navigation.

A digital microscope system dynamically selects full or reduced resolution modes to assemble images based on user-defined areas of interest.

Adjustable optical component manages light polarization states within the imaging beam path.

A ptychographic imaging system adjusts light source emission weights to compensate for geometric effects.

A single mechanical actuator manipulates diffraction orders in the objective lens pupil plane to set precise phase angles for structured illumination microscopy.

Coordinates parallel imaging cycles across detector arrays to resolve throughput bottlenecks in drug discovery workflows.

A STED microscope employs a first-order Bessel beam as the depletion source to maintain focal spot integrity during super-resolution imaging.

Movable frames align LED sources with collimating optics to reduce light loss across multiple wavelengths in fluorescence microscopy.

A bevel wheel and torsion spring drive the pendular arm to align the microscope with each endface, resolving inspection efficiency limits.

A motorized variable optical relay system adjusts illumination beam convergence to correct spherical aberration in non-descanned detection paths.

Dynamic phase pattern control adjusts the inner diameter of the STED light to resolve the trade-off between measurement precision and scanning time.

A wide-field optical microscope employs a pinhole aperture to filter non-parallel light rays and achieve super-magnified imaging.

A microscope control arrangement derives illumination parameters from fluorophore data to render a graphical user interface with dedicated control widgets.

An asymmetrical light sheet illuminates fluorescent markers to enable precise axial localization in 3D microscopy.