Measurement of the Neutron Lifetime by Counting Trapped Protons

We measured the neutron decay lifetime by counting in-beam neutron decay recoil protons trapped in a quasi-Penning trap. The absolute neutron beam fluence was measured by capture in a thin ⁶LiF foil detector with known efficiency. The combination of these measurements gives the neutron lifetime: τ_n = (886.8 ± 1.2 ± 3.2) s, where the first (second) uncertainty is statistical (systematic) in nature. This is the most precise neutron lifetime determination to date using an in-beam method.     

Neutron Lifetime Experiment Based on an Accordion-Like UCN Storage Volume Coated With “Low Temperature Fomblin”

A new type of per-fluorinated polymer, “Low Temperature Fomblin,” has been tested as a wall coating in an ultracold neutron (UCN) storage experiment using a gravitational storage system. The data show a UCN reflection loss coefficient η as low as ≈ 5 × 10⁻⁶ in the temperature range 105 K to 150 K. We plan to use this oil in a new type of neutron lifetime measurement, where a bellows system (“accordion”) enables to vary the trap size in a wide range while the total surface area and distribution of surface area over height remain constant. These unique characteristics, in combination with application of the scaling technique developed by W. Mampe et al. in 1989, ensure exact linearity for the extrapolation from inverse storage lifetimes to the inverse neutron lifetime. Linearity holds for any energy dependence of loss coefficient µ(E). Using the UCN source at the Institut Laue Langevin we expect to achieve a lifetime precision below ±1 s.     

Measurement of the Coherent Neutron Scattering Length of 3He

By means of neutron interferometry the s-wave neutron scattering length of the ³He nucleus was re-measured at the Institut Laue-Langevin (ILL). Using a skew symmetrical perfect crystal Si-interferometer and a linear twin chamber cell, false phase shifts due to sample misalignment were reduced to a negligible level. Simulation calculations suggest an asymmetrically alternating measuring sequence in order to compensate for systematic errors caused by thermal phase drifts. There is evidence in the experiment’s data that this procedure is indeed effective. The neutron refractive index in terms of Sears’ exact expression for the scattering amplitude has been analyzed in order to evaluate the measured phase shifts. The result of our measurement, b′_c = (6.000 ± 0.009) fm, shows a deviation towards a greater value compared to the presently accepted value of b′_c = (5.74 ± 0.07) fm, confirming the observation of the partner experiment at NIST. On the other hand, the results of both precision measurements at NIST and ILL exhibit a serious 12σ (12 standard uncertainties) deviation, the reason for which is not clear yet.     

Can a Pressure Standard be Based on Capacitance Measurements?

We consider the feasibility of basing a pressure standard on measurements of the dielectric constant ϵ and the thermodynamic temperature T of helium near 0 °C. The pressure p of the helium would be calculated from fundamental constants, quantum mechanics, and statistical mechanics. At present, the relative standard uncertainty of the pressure u_r(p) would exceed 20 × 10⁻⁶, the relative uncertainty of the value of the molar polarizability of helium A_ϵ calculated ab initio. If the relativistic corrections to A_ϵ were calculated as accurately as the classical value is now known, a capacitance-based pressure standard might attain u_r(p) < 6 × 10⁻⁶ for pressures near 1 MPa, a result of considerable interest for pressure metrology. One obtains p by eliminating the density from the virial expansions for p and ϵ − 1. If ϵ − 1 were measured with a very stable, 0.5 pF toroidal cross capacitor, the small capacitance and the small values of ϵ − 1 would require state-of-the-art capacitance measurements to achieve a useful pressure standard.     

Treasure of the Past VI: Standard Potential of the Silver-Silver-Chloride Electrode from 0° to 95° C and the Thermodynamic Properties of Dilute Hydrochloric Acid Solutions

From electromotive-force measurements of the cell without liquid junction: Pt;  H₂,  HCl (m),  AgCl;  Agthrough the range 0° to 95° C, calculations have been made of (1) the standard potential of the silver–silver-chloride electrode, (2) the activity coefficient of hydrochloric acid in aqueous solutions from m (molality) =0 to m=0.1 and from 0° to 90° C, (3) the relative partial molal heat content of hydrochloric acid, and (4) the relative partial molal heat capacity of hydrochloric acid.The extrapolations were made by the method of least squares with the aid of punch-card techniques. Data from at least 24 cells were analyzed at each temperature, and 81 cells were studied at 25° C. The value of the standard potential was found to be 0.22234 absolute volt at 25° C, and the standard deviation was 0.02 millivolt at 0° C, 0.01 millivolt at 25° C, and 0.09 millivolt at 95° C. The results from 0° to 60° C are compared with earlier determinations of the standard potential and other quantities derived from the electromotive force.     

A Standard for the Measurement of the pH of Blood and Other Physiological Media

A buffer solution containing potassium dihydrogen phosphate (0.008695 molal) and disodium hydrogen phosphate (0.03043 molal) is proposed as a pH standard for the physiologically important range, pH 7 to 8. The proposed standard solution is prepared by dissolving 1.179 g (air weight) of potassium dihydrogen phosphate and 4.303 g (air weight) of disodium hydrogen phosphate in ammonia-free water and diluting to 1 liter at 25 °C. The ionic strength is 0.1.Standard pH values (pH_s) were assigned to this reference solution at temperatures from 0 to 50 °C by means of emf measurements of hydrogen-silver chloride cells without liquid junction. The activity coefficient of chloride ion, upon which the assignment of pH_s depends, was evaluated by means of a recently proposed convention. By this means, standard values precise to ± 0.001 unit could be derived from the emf data. At 25 °C pH_s is 7.414, and at 38 °C it is 7.382. The operational consistency of these standard values with those for the 0.025-m equimolal phosphate buffer (one of the NBS primary standards) was demonstrated.     

A Ramsey’s Method With Pulsed Neutrons for a T-Violation Experiment

A Ramsey’s method with pulsed neutrons is discussed for neutron spin manipulation in a time reversal (T) symmetry violation experiment. The neutron spin (s_n) is aligned to the direction of a vector product of the nuclear spin (I) and the neutron momentum (k_n) for the measurement of a T-odd correlation term, which is represented as s_n · (k_n × I), during propagation through a polarized nuclear target. The phase control and amplitude modulation of separated oscillatory fields are discussed for the measurement of the T-odd correlation term.     

Standardization of 63Ni by 4πβ Liquid Scintillation Spectrometry With 3H-Standard Efficiency Tracing

The low energy (E_βmax = 66.945 keV ± 0.004 keV) β-emitter ⁶³Ni has become increasingly important in the field of radionuclidic metrology. In addition to having a low β-endpoint energy, the relatively long half-life (101.1 a ± 1.4 a) makes it an appealing standard for such applications. This paper describes the recent preparation and calibration of a new solution Standard Reference Material of ⁶³Ni, SRM 4226C, released by the National Institute of Standards and Technology. The massic activity C_A for these standards was determined using 4πβ liquid scintillation (LS) spectrometry with ³H-standard efficiency tracing using the CIEMAT/NIST method, and is certified as 50.53 kBq ·g⁻¹ ± 0.46 Bq · g⁻¹ at the reference time of 1200 EST August 15, 1995. The uncertainty given is the expanded (coverage factor k = 2 and thus a 2 standard deviation estimate) uncertainty based on the evaluation of 28 different uncertainty components. These components were evaluated on the basis of an exhaustive number (976) of LS counting measurements investigating over 15 variables. Through the study of these variables it was found that LS cocktail water mass fraction and ion concentration play important roles in cocktail stability and consistency of counting results. The results of all of these experiments are discussed.     

Electronic conduction in La-based perovskite-type oxides

A systematic study of La-based perovskite-type oxides from the viewpoint of their electronic conduction properties was performed. LaCo_0.5Ni_0.5O_3±δ was found to be a promising candidate as a replacement for standard metals used in oxide electrodes and wiring that are operated at temperatures up to 1173 K in air because of its high electrical conductivity and stability at high temperatures. LaCo_0.5Ni_0.5O_3±δ exhibits a high conductivity of 1.9 × 10³ S cm⁻¹ at room temperature (R.T.) because of a high carrier concentration n of 2.2 × 10²² cm⁻³ and a small effective mass m∗ of 0.10 m_e. Notably, LaCo_0.5Ni_0.5O_3±δ exhibits this high electrical conductivity from R.T. to 1173 K, and little change in the oxygen content occurs under these conditions. LaCo_0.5Ni_0.5O_3±δ is the most suitable for the fabrication of oxide electrodes and wiring, though La_1−xSr_xCoO_3±δ and La_1−xSr_xMnO_3±δ also exhibit high electronic conductivity at R.T., with maximum electrical conductivities of 4.4 × 10³ S cm⁻¹ for La_0.5Sr_0.5CoO_3±δ and 1.5 × 10³ S cm⁻¹ for La_0.6Sr_0.4MnO_3±δ because oxygen release occurs in La_1−xSr_xCoO_3±δ as elevating temperature and the electrical conductivity of La_0.6Sr_0.4MnO_3±δ slightly decreases at temperatures above 400 K.     

Measurement of the Parity-Violating Neutron Spin Rotation in 4He

In the meson exchange model of weak nucleon-nucleon (NN) interactions, the exchange of virtual mesons between the nucleons is parameterized by a set of weak meson exchange amplitudes. The strengths of these amplitudes from theoretical calculations are not well known, and experimental measurements of parity-violating (PV) observables in different nuclear systems have not constrained their values. Transversely polarized cold neutrons traveling through liquid helium experience a PV spin rotation due to the weak interaction with an angle proportional to a linear combination of these weak meson exchange amplitudes. A measurement of the PV neutron spin rotation in helium (φ_PV (n,α)) would provide information about the relative strengths of the weak meson exchange amplitudes, and with the longitudinal analyzing power measurement in the p + α system, allow the first comparison between isospin mirror systems in weak NN interaction. An earlier experiment performed at NIST obtained a result consistent with zero: φ_PV (n,α) = (8.0 ±14(stat) ±2.2(syst)) ×10⁻⁷ rad / m[1]. We describe a modified apparatus using a superfluid helium target to increase statistics and reduce systematic effects in an effort to reach a sensitivity goal of 10⁻⁷ rad/m.     

Infrared Spectrum of the v2+ v6 Band of C13C12H6

The infrared spectrum of the v₂+v₆ band of C¹³C¹²H₆ has been analyzed and a value of B₀= 0.64865 ±0.00005 cm⁻¹ determined. When this value is combined with that found in recent work on isotopically normal ethane, a “r_s” value of 1.527±0.004 A for the carboncarbon bond distance is obtained. (Uncertainties are probable errors.)     

Measurement of Parity Violation in np Capture: the NPDGamma Experiment

The NPDGamma experiment will measure the parity-violating directional gamma ray asymmetry A_γ in the reaction n→+p→d+γ. Ultimately, this will constitute the first measurement in the neutron-proton system that is sensitive enough to challenge modern theories of nuclear parity violation, providing a theoretically clean determination of the weak pion-nucleon coupling. A new beam-line at the Los Alamos Neutron Science Center (LANSCE) delivers pulsed cold neutrons to the apparatus, where they are polarized by transmission through a large volume polarized ³He spin filter and captured in a liquid para-hydrogen target. The 2.2 MeV gamma rays from the capture reaction are detected in an array of CsI(Tl) scintillators read out by vacuum photodiodes operated in current mode. We will complete commissioning of the apparatus and carry out a first measurement at LANSCE in 2004–05, which would provide a statistics-limited result for A_γ accurate to a standard uncertainty of ±5 × 10⁻⁸ level or better, improving on existing measurements in the neutron-proton system by a factor of 4. Plans to move the experiment to a reactor facility, where the greater flux would enable us to make a measurement with a standard uncertainty of ±1 × 10⁻⁸, are actively being pursued for the longer term.     

Standard Reference Material (SRM 1990) For Single Crystal Diffractometer Alignment

An international project was successfully completed which involved two major undertakings: (1) a round-robin to demonstrate the viability of the selected standard and (2) the certification of the lattice parameters of the SRM 1990, a Standard Reference Material^® for single crystal diffractometer alignment. This SRM is a set of ≈3500 units of Cr-doped Al₂O₃, or ruby spheres [(0.420.011 mole fraction % Cr (expanded uncertainty)]. The round-robin consisted of determination of lattice parameters of a pair of crystals: the ruby sphere as a standard, and a zeolite reference to serve as an unknown. Fifty pairs of crystals were dispatched from Hauptman-Woodward Medical Research Institute to volunteers in x-ray laboratories world-wide. A total of 45 sets of data was received from 32 laboratories. The mean unit cell parameters of the ruby spheres was found to be a=4.7608 ű0.0062 Å, and c=12.9979 ű0.020 Å (95 % intervals of the laboratory means). The source of errors of outlier data was identified. The SRM project involved the certification of lattice parameters using four well-aligned single crystal diffractometers at (Bell Laboratories) Lucent Technologies and at NRC of Canada (39 ruby spheres), the quantification of the Cr content using a combined microprobe and SEM/EDS technique, and the evaluation of the mosaicity of the ruby spheres using a double-crystal spectrometry method. A confirmation of the lattice parameters was also conducted using a Guinier-Hägg camera. Systematic corrections of thermal expansion and refraction corrections were applied. These rubies_– are rhombohedral, with space group R3¯c. The certified mean unit cell parameters are a=4.76080±0.00029 Å, and c=12.99568 ű0.00087 Å (expanded uncertainty). These certified lattice parameters fall well within the results of those obtained from the international round-robin study. The Guinier-Hägg transmission measurements on five samples of powdered rubies (a=4.7610 ű0.0013 Å, and c = 12.9954 ű0.0034 Å) agreed well with the values obtained from the single crystal spheres.     

Interlaboratory Comparison of Magnetic Thin Film Measurements

A potential low magnetic moment standard reference material (SRM) was studied in an interlaboratory comparison. The mean and the standard deviation of the saturation moment m_s, the remanent moment m_r, and the intrinsic coercivity H_c of nine samples were extracted from hysteresis-loop measurements. Samples were measured by thirteen laboratories using inductive-field loopers, vibrating-sample magnetometers, alternating-gradient force magnetometers, and superconducting quantum-interference-device magnetometers. NiFe films on Si substrates had saturation moment measurements reproduced within 5 % variation among the laboratories. The results show that a good candidate for an SRM must have a highly square hysteresis loop (m_r/m_s > 90 %), H_c ≈ 400 A·m⁻¹ (5 Oe), and m_s ≈ 2 × 10⁻⁷ A·m² (2 × 10⁻⁴ emu).     

Determination of the Electron-Antineutrino Angular Correlation Coefficient a0 in Unpolarized Neutron β-Decay

The coefficient a₀ has been derived from a measurement of the integral spectrum of recoil protons stored in a quasi-Penning trap with inhomogeneous magnetic field and adiabatic focusing onto an electro-static mirror of potential variable in 10 V steps between 0 V and 850 V. Correction for incomplete transfer of energy from transverse to longitudinal degrees of freedom, and the violation of the adiabatic conditions on reflection at the mirror, is carried out by alternately measuring the spectrum at trapping times of 1 ms and 2 ms. The results a₀ = −0.1054 ± 0.0055 and |λ | = 1.271 ± 0.018 are comparable in precision with existing measurements of a₀.     

An Absolute Calibration of the National Bureau of Standards Thermal Neutron Flux

The NBS Thermal Neutron Flux has been calibrated in terms of the gold thermal neutron capture cross section. The effective thermal neutron (below cadmium cutoff energy) flux density is estimated to be 4307 ± 2 percent n/cm² sec in September 1961. This figure is in agreement with a recent value quoted by the NBS.     

Absolute Isotopic Abundance Ratios and Atomic Weight of a Reference Sample of Nickel

Absolute values have been obtained for the isotopic abundance ratios of a reference sample of nickel (Standard Reference Material 986), using thermal ionization mass spectrometry. Samples of known isotopic composition, prepared from nearly isotopically pure separated nickel isotopes, were used to calibrate the mass spectrometers. The resulting absolute isotopic ratios are: ⁵⁸Ni/⁶⁰Ni=2.596061±0.000728, ⁶¹Ni/⁶⁰Ni=0.043469±0.000015,⁶²Ni/⁶⁰Ni=0.138600±0.000045, and ⁶⁴Ni/⁶⁰Ni=0.035295±0.000024, which yield atom percents of ⁵⁸Ni=68.076886 ±0.005919, ⁶⁰Ni = 26.223146±0.005144,⁶¹Ni=1.139894±0.000433, ⁶²Ni =3.634528±0.001142, and ⁶⁴Ni =0.925546±0.000599. The atomic weight calculated from this isotopic composition is 58.693353 ±0.000147. The indicated uncertainties are overall limits of error based on two standard deviations of the mean and allowances for the effects of known sources of possible systematic error.     

Acid Dissociation Constant and Related Thermodynamic Quantities for Triethanolammonium Ion in Water From 0 to 50°C

Earlier studies of the dissociation constants of monoethanolammonium and diethanolammonium ions and the thermodynamic constants for the dissociation processes have been supplemented by a similar study of triethanolammonium ion from 0° to 50° C. The dissociation constant (K_bh) is given by the formula ?log K_bh = 1341.16/T + 4.6252 ? 0.0045666Twhere T is in degrees Kelvin. The order of acidic strengths of the ions is as follows: Triethanolammonium >diethanolammonium>monethanolammonium. Conversely, monoethanolamine is the strongest of the three bases. The thermodynamic constants for the dissociation of one mole of triethanolammonium ion in the standard state at 25° C are as follows: Heat content change (ΔH°) 33.450 joule mole⁻¹; entropy change (ΔS°), −36.4 joule deg⁻¹ mole⁻¹; heat-capacity change (ΔCp°), 52 joule deg⁻¹ mole⁻¹.     

Experimental and Theoretical Study of Kinetics of Bulk Crystallization in Poly(Chlorotrifluoroethylene)

The rate of isothermal bulk crystallization of poly(chlorotrifluoroethylene), T_m=221° C, was measured from 170° to 200° C. The intrinsic bulk crystallization, which accurately followed an n = 2 law, was shown to be a result of the injection of primary nuclei sporadically in time, with one-dimensional growth of centers derived from these nuclei. The crystallites are exceedingly small. The one-dimensional growth process was isolated by nucleating specimens with seed crystals, and its temperature-dependence determined between 191° and 205° C. The seed crystal isotherms followed an n = 1 law. The temperature coefficients of the rate of nucleation and the rate of growth were both strongly negative.A theory of homogeneous nucleation that takes into account the segmental character of the polymer chains is developed in some detail. A cylindrical nucleus is assumed. In the temperature range near the melting point, region A, where the radius and length of the nucleus are unrestricted, the rate of nucleation is shown to be proportional to exp(−α/T³ΔT²). The nucleation rate is proportional to exp (−β/T²ΔT) in region B, which extends from somewhat below the melting point to considerably lower temperatures; the length of the nucleus has a constant value l₀ in this region, but the radius is unrestricted. (In the above expressions, α and β are constants). Finally, at sufficiently low temperatures, region C is entered. Under certain circumstances, the rate of nucleation in region C will be extremely rapid, and correspond to a “nucleative collapse” of the supercooled liquid state. A calculation of the one-dimensional growth rate shows that it is proportional to exp(−γ/T²ΔT) where β=γ.A careful analysis of the experimental data obtained between 170° and 200° C clearly showed that both the rate of nucleation and the rate of growth were proportional to exp(−β/T²ΔT), and not exp(−α/T³ΔT²). The primary nucleation event was thus of type B in this interval. A detailed analysis of the data is given, and surface free energies and the dimensions of the nuclei quoted. Quenching experiments, where the polymer was crystallized well below 170° C, gave a firm indication of the existence of region C.An experimental study was made of the extremely slow crystallization process that prevailed when the degree of crystallinity became high. The onset of this stage of the crystallization was interpreted as being the result of a massive degree of impingement. This interpretation is justified by the calculations of Lauritzen, who has given a theory of impingements that predicts a pseudoequilibrium degree of crystallinity.As indicated above, the growth process originating at homogeneous nuclei is not of a three-dimensional or spherulitic character in the region of study. Such stray spherulites as do appear in this region are shown to originate at heterogeneities. The possibility that the intrinsic growth process may become three-dimensional at crystallization temperatures sufficiently near T_m is discussed.     

Phase Equilibrium Relations in the Sc2O3-Ga2O3 System

The phase equilibrium diagram was determined for the Sc₂O₃-Ga₂O₃ system. A quenching furnace, wound with 60 percent Pt—40 percent Rh wire, was employed for experiments conducted at temperatures up to 1,800 °C. An induction furnace, having an iridium crucible susceptor, was used to obtain higher temperatures. Temperatures in the quenching furnace were measured with both an optical pyrometer and a 95 percent Pt—5 percent Rh versus 80 percent Pt—20 percent Rh thermocouple. The melting point of Ga₂O₃ was determined as 1,795 ±15 °C. Experiments at temperatures as high as 2,405 °C failed to melt Sc₂O₃. Two intermediate binary phases, a compound believed to be 6Sc₂O₃·5Ga₂O₃ and a solid solution occur in the system. The solid solution phase appears as a single phase in the region roughly defined by the compositional limits of 55 to 73 mole percent Ga₂O₃ at the solidus. The 6:5 compound, stable only at high temperatures, melts incongruently at 1,770 ±15 °C and decomposes below 1,700 ±15 °C. The compound appears to have orthorhombic symmetry with a=13.85 A, b= 9.80 A, and c=9.58 A. The indicated uncertainties in the melting points are a conservative estimate of the overall inaccuracies.