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NEW MATERIALS DEVELOPED TO MEET REGULATORY AND TECHNICAL REQUIREMENTS ASSOCIATED WITH IN-SITU DECOMMISSIONING OF NUCLEAR REACTORS AND ASSOCIATED FACILITIES

For the 2010 ANS Embedded Topical Meeting on Decommissioning, Decontamination and Reutilization and Technology, Savannah River National Laboratory's Mike Serrato reported initial information on the newly developed specialty grout materials necessary to satisfy all requirements associated with in-situ decommissioning of P-Reactor and R-Reactor at the U.S. Department of Energy's Savannah River Site. Since that report, both projects have been successfully completed and extensive test data on both fresh properties and cured properties has been gathered and analyzed for a total of almost 191,150 m{sup 3} (250,000 yd{sup 3}) of new materials placed. The focus of this paper is to describe the (1) special grout mix for filling the P-Reactor vessel (RV) and (2) the new flowable structural fill materials used to fill the below grade portions of the facilities. With a wealth of data now in hand, this paper also captures the test results and reports on the performance of these new materials. Both reactors were constructed and entered service in the early 1950s, producing weapons grade materials for the nation's defense nuclear program. R-Reactor was shut down in 1964 and the P-Reactor in 1991. In-situ decommissioning (ISD) was selected for both facilities and performed as Comprehensive Environmental Response, Compensations and Liability Act actions (an early action for P-Reactor and a removal action for R-Reactor), beginning in October 2009. The U.S. Department of Energy concept for ISD is to physically stabilize and isolate intact, structurally robust facilities that are no longer needed for their original purpose of producing (reactor facilities), processing (isotope separation facilities), or storing radioactive materials. Funding for accelerated decommissioning was provided under the American Recovery and Reinvestment Act. Decommissioning of both facilities was completed in September 2011. ISD objectives for these CERCLA actions included: (1) Prevent industrial worker exposure to radioactive or hazardous contamination exceeding Principal Threat Source Material levels; (2) Minimize human and ecological exposure to unacceptable risk associated with radiological and hazardous constituents that are or may be present; (3) Prevent to the extent practicable the migration of radioactive or hazardous contaminants from the closed facility to the groundwater so that concentrations in groundwater do not exceed regulatory standards; (4) Eliminate or control all routes of human exposure to radiological and chemical contamination; and (5) Prevent animal intruder exposure to radioactive and hazardous contamination.

22 GENERAL STUDIES OF NUCLEAR REACTORS↗

Effect of sepiolite on the flocculation of suspensions of fibre-reinforced cement

Sepiolite is used to increase thixotropy of cement slurries for easier processing, to prevent sagging and to provide a better final quality in the manufacture of fibre-reinforced cement products. However, the effect of sepiolite on flocculation and its interactions with the components of fibre cement are yet unknown. The aim of this research is to study the effects of sepiolite on the flocculation of different fibre-reinforced cement slurries induced by anionic polyacrylamides (A-PAMs). Flocculation and floc properties were studied by monitoring the chord size distribution in real time employing a focused beam reflectance measurement (FBRM) probe. The results show that sepiolite increases floc size and floc stability in fibre-cement suspensions. Sepiolite competes with fibres and clay for A-PAMs adsorption and its interaction with A-PAM improves flocculation of mineral particles.

36 MATERIALS SCIENCE↗

Bayesian calibration of thermodynamic parameters for geochemical speciation modeling of cementitious materials

Chemical equilibrium modeling of cementitious materials requires aqueous-solid equilibrium constants of the controlling mineral phases (K{sub sp}) and the available concentrations of primary components. Inherent randomness of the input and model parameters, experimental measurement error, the assumptions and approximations required for numerical simulation, and inadequate knowledge of the chemical process contribute to uncertainty in model prediction. A numerical simulation framework is developed in this paper to assess uncertainty in K{sub sp} values used in geochemical speciation models. A Bayesian statistical method is used in combination with an efficient, adaptive Metropolis sampling technique to develop probability density functions for K{sub sp} values. One set of leaching experimental observations is used for calibration and another set is used for comparison to evaluate the applicability of the approach. The estimated probability distributions of K{sub sp} values can be used in Monte Carlo simulation to assess uncertainty in the behavior of aqueous-solid partitioning of constituents in cement-based materials.

36 MATERIALS SCIENCE↗

Phosphate-intercalated Ca-Fe-layered double hydroxides: Crystal structure, bonding character, and release kinetics of phosphate

The nitrate-form of Ca-Fe-layered double hydroxide (Ca-Fe-LDH) was synthesized via co-precipitation method, and its phosphate-intercalates were prepared by ion-exchange reaction. According to X-ray diffraction analysis, the Ca-Fe-LDH-NO{sub 3}{sup -} compound and its H{sub 2}PO{sub 4}{sup -}-intercalate showed hexagonal layered structures, whereas the ion-exchange reaction with HPO{sub 4}{sup 2-} caused a frustration of the layer ordering of LDH. Fe K-edge X-ray absorption spectroscopy clearly demonstrated that the Ca-Fe-LDH lattice with trivalent iron ions was well-maintained after the ion-exchange with HPO{sub 4}{sup 2-} and H{sub 2}PO{sub 4}{sup -}. Under acidic conditions, phosphate ions were slowly released from the Ca-Fe-LDH lattice and the simultaneous release of hydroxide caused the neutralization of acidic media. Fitting analysis based on kinetic models indicated a heterogeneous diffusion process of phosphates and a distinct dependence of release rate on the charge of phosphates. This study strongly suggested that Ca-Fe-LDH is applicable as bifunctional vector for slow release of phosphate fertilizer and for the neutralization of acid soil. -- Graphical abstract: We synthesized phosphate-intercalated Ca-Fe-LDH materials that can act as bifunctional inorganic vectors for the slow release of phosphate fertilizer and also the neutralization of acid soil. Fitting analysis based on kinetic models indicated a heterogeneous diffusion process of phosphates and a distinct dependence of release rate on the charge of phosphates. Display Omitted Research Highlights: {yields} The phosphate forms of Ca-Fe-layered double hydroxide (Ca-Fe-LDH) were synthesized via co-precipitation method. The crystal structure, bonding character, and release kinetics of phosphate of the phosphate-intercalates were investigated. These Ca-Fe-LDH materials are applicable as bifunctional vector for slow release of phosphate fertilizer and for the neutralization of acid soil.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

NDA Challenges during Cleanup of the Hanford 618-10 Burial Ground Trenches - 15542

The 618-10 Burial Ground on the Hanford Reservation was an early trench waste site used for the disposal of waste from the 300 Area at Hanford. Much of this waste consisted of residues from evaluations of failed fuel as well as various process and separations studies associated with the Department of Energy (DOE) mission which were performed in the 300 Area between March 1954 and September 1963. Much of this waste contained significant concentrations of fission products as well as Transuranic (TRU) radionuclides. Waste forms consist of drums and boxes which were disposed of in the trenches. Many of the drums are shielded containers, cemented sludge, or cemented debris. There are no identifying marks on the containers to correlate them to a specific waste stream. In addition there is some waste in the trenches which came from other locations outside of the 300 area. Cleanup of the 618-10 burial ground is covered under the Washington Closure Hanford (WCH) contract. Due to the proximity of the 618-10 site to the Columbia River, waste is being removed from the 618-10 site, stabilized, and disposed of into either the Environmental Restoration Disposal Facility (ERDF) if the containers are determined to be LLW or transferred to the Hanford Central Waste Complex (CWC) if the containers are suspected to be TRU waste. In order to determine the correct disposal path Non Destructive Assay (NDA) must be performed on all of the containers excavated from the trenches. The NDA of these containers is performed using germanium gamma spectroscopy with an In Situ Object Counting System (ISOCS) and with a neutron slab counter. Due to the challenges associated with these difficult waste streams, matrices, and lack of information to associate these containers with a particular process, the NDA program has had to develop a more robust process to ensure the correct disposition of the waste. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

Ultrasonic properties of low solvus high refractory (LSHR) super alloy disk material

Measurements are made for ultrasonic linear and nonlinear properties of the powder metallurgy disk alloy LSHR material designed with a relatively low {gamma}' precipitate solvus temperature and high refractory element content. This allows versatile heat treatment processing which results in high tensile, creep and fatigue properties depending on the grain size controlled through proper selection of solution heat treatment temperatures relative to the {gamma}' precipitate solvus temperature. Sound velocity and attenuation for both longitudinal and shear modes at various frequencies from 5 to 20 MHz help to identify and quantify the size of transition zone nondestructively between the small grain ({approx}10 {mu}m) and the large grain ({approx}100 {mu}m) zones. The shear wave velocity measurements taken by aligning the transducer polarization direction parallel and perpendicular to the grain transition direction reveal some results that we do not fully understand at this time and will be the basis of future research. Similarly, measurements of the acoustic nonlinearity parameter show some variations that may originate from uncertain sources.

36 MATERIALS SCIENCE↗

Dissimilar Friction Stir Welds in Al5186-Al2024: The Effect of Process Parameters on Microstructures and Mechanical Properties

The effect of tool traverse and rotation speeds on the microstructures and mechanical properties are quantified for welds between non-age-hardening Al5083 and age hardening Al2024 and compared to single alloy joints made from each of the two constituents. In this paper, we report the results of microstructural, mechanical property investigations of Al5186-Al2024 friction stir welds produced using various rotations and traveling speeds of the tool to investigate the effects of the welding parameters on the joint strength. Metallographic studies by optical microscopy, electron probe microscopy, and the utilization of the X-ray diffraction technique have been conducted. It was found that the weld properties were dominated by the thermal input rather than the mechanical deformation by the tool. In particular the larger stresses under the weld tool on the AA5186 side compared to the AA2024 side are related to a transient reduction in yield stress due to dissolution of the hardening precipitates during welding prior to natural aging after welding.

36 MATERIALS SCIENCE↗

Leaky ion extraction method for dielectronic recombination strength measurements at electron-beam ion traps

There are a number of mechanisms via which ions and electrons interact in a plasma, but by far one of the most important is through dielectronic recombination (DR). This is a resonant process through which an ion can capture a free electron and decrease its charge by one unit. Cross sections or strengths for this process are of vital importance in the modeling of hot plasmas and hence any advance in measurement or calculation procedures for obtaining DR data is of great importance. The work presented here examines the underlying basis of a newly developed method based on leaky mode ion extraction from an electron beam ion trap (EBIT), for relatively quickly obtaining DR strengths. The development attains to use the ratio of the leaked ions in adjacent charge states, i.e., the initial and final charge states of a DR process, to obtain the strengths preassuming that this ratio is the same as that of the ions remaining inside the EBIT trap. This work shows this assumption to be false. Hence DR strengths measured using leaked ions may be subject to error. But this work also reveals that the difference between this ratio and the one for trapped ions is insensitive to most of the experimental conditions, which means reliable DR strengths can still be obtained by leaky mode ion extraction if proper corrections are applied. An example is shown in this paper where after correction of some experimental results for DR strengths, obtained using the leaky mode, excellent agreement with corresponding theoretical calculations is obtained.

70 PLASMA PHYSICS AND FUSION TECHNOLOGY↗

HEAVY-ION FRACTIONATION IN THE IMPULSIVE SOLAR ENERGETIC PARTICLE EVENT OF 2002 AUGUST 20: ELEMENTS, ISOTOPES, AND INFERRED CHARGE STATES

Measurements of heavy-ion elemental and isotopic composition in the energy range {approx}12-60 MeV nucleon{sup -1} are reported from the Advanced Composition Explorer/Solar Isotope Spectrometer (ACE/SIS) instrument for the solar energetic particle (SEP) event of 2002 August 20. We investigate fractionation in this particularly intense impulsive event by examining the enhancements of elemental and isotopic abundance ratios relative to corresponding values in the solar wind. The elemental enhancement pattern is similar to those in other impulsive events detected by ACE/SIS and in compilations of average impulsive-event composition. For individual elements, the abundance of a heavy isotope (mass M {sub 2}) is enhanced relative to that of a lighter isotope (M{sub 1}) by a factor {approx}(M {sub 1}/M {sub 2}){sup {alpha}} with {alpha} {approx_equal} -15. Previous studies have reported elemental abundance enhancements organized as a power law in Q/M, the ratio of estimated ionic charge to mass in the material being fractionated. We consider the possibility that a fractionation law of this form could be responsible for the isotopic fractionation as a power law in the mass ratio and then explore the implications it would have for the ionic charge states in the source material. Assuming that carbon is fully stripped (Q{sub C} = 6), we infer mean values of the ionic charge during the fractionation process, Q{sub Z} , for a variety of elements with atomic numbers 7 {<=} Z {<=} 28. We find that Q{sub Fe} {approx_equal} 21-22, comparable to the highest observed values that have been reported at lower energies in impulsive SEP events from direct measurements near 1 AU. The inferred charge states as a function of Z are characterized by several step increases in the number of attached electrons, Z - Q{sub Z} . We discuss how this step structure, together with the known masses of the elements, might account for a variety of features in the observed pattern of elemental abundance enhancements. We also briefly consider alternative fractionation laws and the relationship between the charge states we infer in the source material and those derived from in situ observations.

79 ASTRONOMY AND ASTROPHYSICS↗

The induction of a graphite-like phase on diamond films by a Fe-coating/post-annealing process to improve their electron field emission properties

The electron field emission (EFE) process for diamond films was tremendously enhanced by Fe-coating and post-annealing processes. Microstructural analysis indicates that the mechanism for the improvement in the EFE process is the formation of nanographites with good crystallinity that surround the Fe (or Fe{sub 3}C) nanoclusters. Presumably the nanographites were formed via the reaction of Fe clusters with diamond films, viz. by the dissolution of carbons into Fe (or Fe{sub 3}C) clusters and the reprecipitation of carbon species to the surface of the clusters, a process similar to the growth of carbon nanotubes via Fe clusters as catalyst. Not only is a sufficiently high post-annealing temperature (900 deg. C) required but also a highly active reducing atmosphere (NH{sub 3}) is needed to give a proper microstructure for enhancing the EFE process. The best EFE properties are obtained by post-annealing the Fe-coated diamond films at 900 deg. C in an NH{sub 3} environment for 5 min. The EFE behavior of the films can be turned on at E{sub 0} = 1.9 V/{mu}m, attaining a large EFE current density of 315 {mu}A/cm{sup 2} at an applied field of 8.8 V/{mu}m (extrapolation using the Fowler-Nordheim model leads to J{sub e} = 40.7 mA/cm{sup 2} at a 20 V/{mu}m applied field).

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

DNA compaction by azobenzene-containing surfactant

We report on the interaction of cationic azobenzene-containing surfactant with DNA investigated by absorption and fluorescence spectroscopy, dynamic light scattering, and atomic force microscopy. The properties of the surfactant can be controlled with light by reversible switching of the azobenzene unit, incorporated into the surfactant tail, between a hydrophobic trans (visible irradiation) and a hydrophilic cis (UV irradiation) configuration. The influence of the trans-cis isomerization of the azobenzene on the compaction process of DNA molecules and the role of both isomers in the formation and colloidal stability of DNA-surfactant complexes is discussed. It is shown that the trans isomer plays a major role in the DNA compaction process. The influence of the cis isomer on the DNA coil configuration is rather small. The construction of a phase diagram of the DNA concentration versus surfactant/DNA charge ratio allows distancing between three major phases: colloidally stable and unstable compacted globules, and extended coil conformation. There is a critical concentration of DNA above which the compacted globules can be hindered from aggregation and precipitation by adding an appropriate amount of the surfactant in the trans configuration. This is because of the compensation of hydrophobicity of the globules with an increasing amount of the surfactant. Below the critical DNA concentration, the compacted globules are colloidally stable and can be reversibly transferred with light to an extended coil state.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Development of a method for high LET irradiation of liquid systems

A variety of processes, from material sterilization and cancer treatment to used nuclear fuel recycling, benefit from quantifying the sensitivity of the system to radiation. Determining the effects of alpha irradiation on a system may be of complementary interest to the effects of gamma irradiation, as alpha radiation has higher linear energy transfer (LET) and will likely result in different chemical damage effects. This becomes important in advanced nuclear fuel cycle processes where the radioactive materials to be handled in solutions contain significant amounts of alpha emitters. In this work, we describe a method for studying high LET radiation in a liquid system using a TRIGA® reactor and the 10 B(n,α) 7 Li reaction. By fitting a model based on neutron diffusion and absorption to experimentally obtained Fricke dosimetry data, the high LET dose to a sample was predictable over the full range of reactor power available and varying 10 B concentration. This method may be applied to study the effects of high LET radiation on any liquid system as long as a suitable molecule containing boron is used and appropriate neutron diffusion coefficients are known. A wide range of high LET dose rates from <10 Gy/h to >1,000 kGy/h may be obtained with this method.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗

Increase in the Tb{sup 3+} green emission in SiO{sub 2}-LaF{sub 3} nano-glass-ceramics by codoping with Dy{sup 3+} ions

95SiO{sub 2}-5LaF{sub 3} sol-gel derived nano-glass-ceramics single doped with 0.1Dy{sup 3+} or 0.1Tb{sup 3+} mol % and codoped with 0.1Dy{sup 3+} and xTb{sup 3+} (x=0.1,0.3) mol % were successfully obtained. XRD and HRTEM measurements confirm the precipitation of LaF{sub 3} nanocrystals during the ceramming process, with mean size ranging from 10 to 20 nm and increasing with the thermal treatment temperature. About 75% of lanthanide ions are partitioned into LaF{sub 3} nanocrystals, as calculated from luminescence decays. The effect of increasing the Tb{sup 3+} concentration and also of codoping with Dy{sup 3+} in the Tb{sup 3+} green emission from the {sup 5}D{sub 4} level have been studied. The energy transfer mechanisms between Tb{sup 3+} ions and also between Tb{sup 3+}-Dy{sup 3+} ions, which favor the green emission, have been analyzed.

36 MATERIALS SCIENCE↗

Testing nuclear parton distributions with pA collisions at the TeV scale

Global perturbative QCD analyses, based on large data sets from electron-proton and hadron collider experiments, provide tight constraints on the parton distribution function (PDF) in the proton. The extension of these analyses to nuclear parton distribution functions (nPDFs) has attracted much interest in recent years. nPDFs are needed as benchmarks for the characterization of hot QCD matter in nucleus-nucleus collisions, and attract further interest since they may show novel signatures of nonlinear density-dependent QCD evolution. However, it is not known from first principles whether the factorization of long-range phenomena into process-independent parton distribution, which underlies global PDF extractions for the proton, extends to nuclear effects. As a consequence, assessing the reliability of nPDFs for benchmark calculations goes beyond testing the numerical accuracy of their extraction and requires phenomenological tests of the factorization assumption. Here, we argue that a proton-nucleus collision program at the Large Hadron Collider would provide a set of measurements, which allow for unprecedented tests of the factorization assumption, underlying global nPDF fits.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗

Study of the Adsorption Space of Modified Clinoptilolites

Carbon dioxide (CO 2 ) adsorption is an important adsorbent characterization method and a significant industrial process. In separation and recovery technology, the adsorption of the CO 2 is important to reduce the concentration of this gas considered as one of the greenhouse gases. Natural zeolites, particularly clinoptilolite, are widely applied as adsorbents. In the present research, the structure, composition and morphology of modified with hexafluorosilicate (HFSi) and orthophosphoric acid (H 3 PO 4 ) clinoptilolites were investigated by characterizations and measurements made with, X-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscopy-energy dispersive X-ray analysis (SEM-EDAX) and gravimetric adsorption. In addition, the surface Chemistry of the modified clinoptilolites was analyzed by applying diffuse reflectance fourier transform infrared spectrometry (DRIFTS). Further, the interaction of CO 2 within the adsorption space of these modified clinoptilolites and a synthetic ZSM-5 zeolite was studied with the help of adsorption measurements. An appropriate theoretical methodology for the analysis of the XRD and adsorption data was applied. The calculated cell parameters of the tested are similar to those reported for a typical clinoptilolite of: a = 17.662 Å, b = 17.911 Å, c = 7.407 Å and β = 116.40 The resolution of the TGA derivative profiles indicated the presence of two steps for water release, one of them represents the loss of majority of the water present in the micropores. This was evidenced as a broad peak centered at about 50°C for the CSW-HFSi-0.1, but at 100 °C for the samples CSW-HFSi-0.4. The SEM micrographs corresponding to the modified clinoptilolites, was evidenced that the CSW zeolite shows secondary particles exhibiting diameters from 3 to 40 μm, formed by primary clinoptilolite crystallites showing a crystallite size, Φ = 40 nm. The EDAX elemental analysis it can be demonstrated that the exchange process replaced about 85% of the charge compensating ions. The DRIFT spectra of the modified clinoptilolites, specifically, CSW-HFSi-0.1, show a narrow band at about: 3,740 cm-l corresponding to terminal silanol groups (Si-OH) and a band 3,600-3,650 cm -1 resulting from extra-framework Al-OH. With the precision of the measured micropore volumes related to the excellent fitting of the adsorption data by the D-R isotherm equation, it can be affirm that carbon adsorption took only place in the micropore region. The isosteric heat of adsorption calculated for the modified clinoptilolites was greater than those values reported of ZSM-5 zeolite, particle packing silica, dealuminated Y zeolite (DAY) Cd, Zn and Ni-nitroprussides and Cu-nitroprusside and a Ni-MOF. With the obtained result it can be concluded that the modified clinoptilolites with HFSi showed a quality as adsorbent comparable to commercial synthetic zeolites.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Numerical analysis of electronegative plasma in the extraction region of negative hydrogen ion sources

This numerical study focuses on the physical mechanisms involved in the extraction of volume-produced H{sup -} ions from a steady state laboratory negative hydrogen ion source with one opening in the plasma electrode (PE) on which a dc-bias voltage is applied. A weak magnetic field is applied in the source plasma transversely to the extracted beam. The goal is to highlight the combined effects of the weak magnetic field and the PE bias voltage (upon the extraction process of H{sup -} ions and electrons). To do so, we focus on the behavior of electrons and volume-produced negative ions within a two-dimensional model using the particle-in-cell method. No collision processes are taken into account, except for electron diffusion across the magnetic field using a simple random-walk model at each time step of the simulation. The results show first that applying the magnetic field (without PE bias) enhances H{sup -} ion extraction, while it drastically decreases the extracted electron current. Secondly, the extracted H{sup -} ion current has a maximum when the PE bias is equal to the plasma potential, while the extracted electron current is significantly reduced by applying the PE bias. The underlying mechanism leading to the above results is the gradual opening by the PE bias of the equipotential lines towards the parts of the extraction region facing the PE. The shape of these lines is due originally to the electron trapping by the magnetic field.

70 PLASMA PHYSICS AND FUSION TECHNOLOGY↗

Model-independent determination of the axial mass parameter in quasielastic neutrino-nucleon scattering

Quasielastic neutrino-nucleon scattering is a basic signal process for neutrino oscillation studies. At accelerator energies, the corresponding cross section is subject to significant uncertainty due to the poorly constrained axial-vector form factor of the nucleon. A model-independent description of the axial-vector form factor is presented. Data from the MiniBooNE experiment for quasielastic neutrino scattering on {sup 12}C are analyzed under the assumption of a definite nuclear model. The value of the axial mass parameter, m{sub A}=0.85{sub -0.07}{sup +0.22}{+-}0.09 GeV, is found to differ significantly from extractions based on traditional form factor models. Implications for future neutrino scattering and pion electroproduction measurements are discussed.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗

Exclusive pp{yields}nn{pi}{sup +}{pi}{sup +} reaction at LHC and RHIC

We evaluate differential distributions for the four-body pp{yields}nn{pi}{sup +}{pi}{sup +} reaction. The amplitude for the process is calculated in the Regge approach including many diagrams. We make predictions for possible future experiments at RHIC and LHC energies. Very large cross sections are found which is partially due to interference of a few mechanisms. Presence of several interfering mechanisms precludes extraction of the elastic {pi}{sup +}{pi}{sup +} scattering cross section. Absorption effects are estimated. Differential distributions in pseudorapidity, rapidity, invariant two-pion mass, transverse-momentum and energy distributions of neutrons are presented for proton-proton collisions at {radical}(s)=500 GeV (RHIC) and {radical}(s)=0.9, 2.36 and 7 TeV (LHC). Cross sections with experimental cuts are presented.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗