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Showing 1321–1350 of 1709 reference entries

MeasurementBACON optical ratios · Precision and disagreement

Aeppli and collaborators' archived 2025/2026 report compares 27Al⁺, 171Yb and 87Sr optical clocks with reported total fractional ratio uncertainties at or below 3.2×10⁻¹⁸.

Empirical finding
MeasurementNetwork covariance and common reference limits

For linear observations z=Aθ+ε with known positive-definite covariance Σ and full-column-rank A, generalized least squares yields θ̂=(AᵀΣ⁻¹A)⁻¹AᵀΣ⁻¹z.

Method
MeasurementHierarchical drift and excess scatter

A network model can include per-instrument offsets, temporal drift, shared-reference effects and between-day variability alongside statistical noise.

Method
MeasurementModel discrepancy, calibration and predictive uncertainty

A discrepancy term δ(x) represents inadequacy of the physical response model, distinct from repeatability noise and uncertain calibration parameters.

Method
MeasurementCertified, reference and research-grade materials

Reference-material value assignments have distinct status.

Definition
MeasurementSRM 1947a · Property-specific certification (May 2026)

The 12 May 2026 NIST certificate for Great Lakes Fish Tissue certifies total mercury and selected PCB, pesticide and PBDE values on a wet-mass basis.

Empirical finding
MeasurementHigh-temperature radiometry and transfer uncertainty

Detector-based radiation thermometry infers thermodynamic temperature from calibrated spectral radiance, while transfer thermometers and blackbody realizations disseminate a scale.

Method
PhysicsA mixing-layer benchmark and observable dependence

Nichols' worked compressible mixing-layer comparison specifies two streams, geometry, initial transients and statistical sampling before comparing RANS, LES and hybrid predictions with measurements downstream.

Method
ChemistryVariational bounds and their limits

For a normalized trial state of the same Hermitian, lower-bounded Hamiltonian, the Rayleigh energy cannot be below its ground-state energy.

Mathematical statement
ChemistryBasis convergence and extrapolation

Basis convergence must be tested separately for SCF and correlation contributions.

Method
ChemistrySCF convergence versus electronic stability

Small energy and orbital-gradient residuals identify a stationary SCF solution, which may be unstable to allowed orbital rotations.

Method
ChemistryFunctional and dispersion error

A larger orbital basis does not remove exchange-correlation functional error.

Approximation
ChemistryCounterpoise and fragment interaction energies

Counterpoise compares the complex energy with fragment energies evaluated in the complex basis, including partner basis functions without partner nuclei.

Method
ChemistryFailure of a single electronic surface

Near electronic degeneracy, nuclear motion can couple electronic states through derivative couplings, so a single Born–Oppenheimer potential surface can fail.

Model
ChemistryFrom electronic excitation energies to spectra

A computed vertical electronic excitation is not automatically a measured spectral maximum.

Method
ChemistryTransmission coefficient and recrossing

In classical transition-state trajectory counting, recrossing the dividing surface reduces the fraction of nominal crossings that contributes to net reaction; this recrossing transmission coefficient is bounded by one.

Model
ChemistryDiffusive barrier crossing and friction

In an overdamped diffusive reaction-coordinate model, the flux contains both potential-driven drift and concentration spreading.

Model
ChemistryMarcus reorganization and competing rate regimes

The classical harmonic reorganization model gives an electron-transfer barrier depending jointly on driving force and reorganization energy.

Model
ChemistryActivity and electrochemical potential gradients

Species transport is driven by chemical and electrical contributions to electrochemical potential.

Mathematical statement
ChemistryDilute Nernst–Planck transport

A dilute-solution Nernst–Planck flux combines diffusion, electric migration and convection.

Model
ChemistryConcentrated electrolyte cross-transport

Stefan–Maxwell transport represents friction between different species rather than independent dilute diffusion through an inert solvent.

Model
ChemistrySeparating electrode kinetics from transport

Current–potential data can reflect charge transfer, bulk migration/diffusion, homogeneous reactions and evolving surface structure.

Method
ChemistryDispersity as a distribution ratio

Molar-mass dispersity is the ratio of mass-average to number-average molar mass.

Definition
ChemistrySize-exclusion calibration and molar mass

Size-exclusion results depend on column, solvent and calibration, so retention-based molar masses are not intrinsically absolute.

Method
ChemistryNetwork gelation beyond linear step growth

Branching models locate gelation when continuing connections become self-sustaining.

Model
ChemistryMaxwell viscoelastic constitutive response

A Maxwell spring and dashpot in series predicts exponential stress relaxation with a characteristic time.

Model
ChemistryStorage and loss moduli

For linear harmonic loading, the complex modulus separates in-phase elastic storage from quadrature viscous loss.

Definition
ChemistryDiffraction intensities and the phase problem

Corrected diffraction intensities constrain squared structure-factor amplitudes, while phases remain essential for reconstructing electron density.

Method
ChemistryPhasing and independent structural checks

Phase probabilities and map weighting affect reconstructed density, and model-derived phases can bias the apparent support for that same model.

Method
ChemistryVibronic coherence: a Br2+ case study

The Br2+ attosecond study reports coherent vibronic signals and interprets their evolution using electronic/nuclear modeling with anharmonic and spin–orbit contributions.

Empirical finding
ModelSource checked

Network gelation beyond linear step growth

Chemistry

Research context

postgraduate concept · conditional · As of 2026-10-10

Branching models locate gelation when continuing connections become self-sustaining.

Key knowledge

Branching models locate gelation when continuing connections become self-sustaining. Functionality, stoichiometric balance and unequal conversions alter the branching probability; physical gels additionally need reversible-association and timescale descriptions.

Conditions and scope

  • Ideal branching calculations assume specified reactivity and neglected cyclic intramolecular loops; a model gel point is not a universal measured viscosity threshold.
Sources · 2

References

Sources retain their recorded scope. A source link alone does not establish verification of every statement.

  1. Networks, Gels, and Rubber ElasticityChapter extract: Networks, Gels, and Rubber ElasticityCourse notes · PDFtaner.balikesir.edu.trRead source
  2. Gold Book: gelIUPACReference guidegoldbook.iupac.orgRead source

Evidence and review

Networks, Gels, and Rubber Elasticity: Branching coefficient, functionality and gel-point probability (extracted pages 694–697; authorship not stated in hosted extract); Gold Book: gel: Network/gel definition including covalent and physical aggregation (definition entry)

2026-10-10 · Bounded author source inspection of network gelation beyond linear step growth, including the stated conditions; independent branch review is recorded separately.

Entry detailsPermanent link to this entry ↗
Record identity
res-chem-gel-point
Revision
research.1
Structured reference record
Postgraduate & research reference