Relevant bibliographies by topics / Boron

Academic literature on the topic 'Boron'

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Published: 4 June 2021
Last updated: 7 July 2024

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Journal articles on the topic "Boron"

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Sokmen, Nihal, and Banu Yeşim Buyukakinci. "THE USAGE OF BORON/ BORON COMPOUNDS IN THE TEXTILE INDUSTRY AND ITS SITUATION IN TURKEY." CBU International Conference Proceedings 6 (September 25, 2018): 1158–65. http://dx.doi.org/10.12955/cbup.v6.1309.

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Commonly found in the earth’s crust, boron happens to be the 51st element of the periodic table and is not found in its elemental state in nature. It is known that there are about 230 different boron minerals in nature. Turkey has the largest boron reserves in the world. In addition to this, Turkey’s boron minerals have the highest quality and production conditions that are more economical than other boron producing countries. For this reason, boron has great importance for Turkey and there is a significant demand for new areas of usage so that Turkey would be able to contribute to the national economy with these resources. The institute of BOREN (National Boron Research Institute) was established for this purpose in Turkey. This institute funds related projects for the extension of boron usage areas. One of the open sectors for innovation is textile technology.This study investigates the history of boron and its current situation in Turkey as well as the studies conducted regarding boron and its compounds especially in the textile field. Taking the available boron reserves in Turkey into consideration, the need for more research and development studies on boron as an environment-friendly element is clear for the textile industry.
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Fujikawa, Yoshiki, Yusuke Fukuo, Kai Nishimura, Kohei Tsujino, Hideki Kashiwagi, Ryo Hiramatsu, Naosuke Nonoguchi, et al. "Evaluation of the Effectiveness of Boron Neutron Capture Therapy with Iodophenyl-Conjugated closo-Dodecaborate on a Rat Brain Tumor Model." Biology 12, no. 9 (September 15, 2023): 1240. http://dx.doi.org/10.3390/biology12091240.

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High-grade gliomas present a significant challenge in neuro-oncology because of their aggressive nature and resistance to current therapies. Boron neutron capture therapy (BNCT) is a potential treatment method; however, the boron used by the carrier compounds—such as 4-borono-L-phenylalanine (L-BPA)—have limitations. This study evaluated the use of boron-conjugated 4-iodophenylbutanamide (BC-IP), a novel boron compound in BNCT, for the treatment of glioma. Using in vitro drug exposure experiments and in vivo studies, we compared BC-IP and BPA, with a focus on boron uptake and retention characteristics. The results showed that although BC-IP had a lower boron uptake than BPA, it exhibited superior retention. Furthermore, despite lower boron accumulation in tumors, BNCT mediated by BC-IP showed significant survival improvement in glioma-bearing rats compared to controls (not treated animals and neutrons only). These results suggest that BC-IP, with its unique properties, may be an alternative boron carrier for BNCT. Further research is required to optimize this potential treatment modality, which could significantly contribute to advancing the treatment of high-grade gliomas.
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COLAK, Bugra, Ahmet KORKMAZ, and Ayhan HORUZ. "BORON STATUS, BORON FRACTIONS AND ITS AVAILABILITY IN SUGAR BEET GROWN SOILS." ANADOLU JOURNAL OF AGRICULTURAL SCIENCES 28, no. 3 (October 5, 2013): 157–67. http://dx.doi.org/10.7161/anajas.2013.28.3.157.

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Kondo, Naoya, Erika Aoki, Shinya Takada, and Takashi Temma. "A Red-Emitting Fluorescence Sensor for Detecting Boronic Acid-Containing Agents in Cells." Sensors 22, no. 19 (October 10, 2022): 7671. http://dx.doi.org/10.3390/s22197671.

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The amount and localization of boron-10 atoms delivered into tumor cells determines the therapeutic effect of boron neutron capture therapy (BNCT) and, consequently, efforts have been directed to develop fluorescence sensors to detect intracellular boronic acid compounds. Currently, these sensors are blue-emitting and hence are impracticable for co-staining with nucleus staining reagents, such as DAPI and Hoechst 33342. Here, we designed and synthesized a novel fluorescence boron sensor, BS-631, that emits fluorescence with a maximum emission wavelength of 631 nm after reaction with the clinically available boronic acid agent, 4-borono-l-phenylalanine (BPA). BS-631 quantitatively detected BPA with sufficiently high sensitivity (detection limit = 19.6 µM) for evaluating BNCT agents. Furthermore, BS-631 did not emit fluorescence after incubation with metal cations. Notably, red-emitting BS-631 could easily and clearly visualize the localization of BPA within cells with nuclei co-stained using Hoechst 33342. This study highlights the promising properties of BS-631 as a versatile boron sensor for evaluating and analyzing boronic acid agents in cancer therapy.
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Nemchenok, I. B. "Boron-loaded liquid scintillator." Functional materials 20, no. 3 (September 25, 2013): 300–303. http://dx.doi.org/10.15407/fm20.03.300.

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Sironi, Maurizio, Mario Raimondi, David L. Cooper, and Joseph Gerratt. "Electronic structure of diborane and octahydrotriborate(1-): boron-hydrogen-boron bridges and closed boron-boron-boron bonds." Journal of Physical Chemistry 95, no. 26 (December 1991): 10617–23. http://dx.doi.org/10.1021/j100179a024.

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Frenking, G., and N. Holzmann. "A Boron-Boron Triple Bond." Science 336, no. 6087 (June 14, 2012): 1394–95. http://dx.doi.org/10.1126/science.1224003.

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Johnson, A. L. "Boron." Annual Reports Section "A" (Inorganic Chemistry) 102 (2006): 59. http://dx.doi.org/10.1039/b508354k.

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Johnson, Andrew L. "Boron." Annual Reports Section "A" (Inorganic Chemistry) 105 (2009): 75. http://dx.doi.org/10.1039/b818136p.

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Banks, Alton. "Boron." Journal of Chemical Education 67, no. 1 (January 1990): 14. http://dx.doi.org/10.1021/ed067p14.

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Dissertations / Theses on the topic "Boron"

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Brain, Paul Terence. "Studies of some compounds containing boron-boron bonds." Thesis, University of Oxford, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.291091.

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Zhu, Xiaojing. "Processability of Nickel-Boron Nanolayer Coated Boron Carbide." Diss., Virginia Tech, 2008. http://hdl.handle.net/10919/28633.

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This dissertation work focuses on the processability improvement of B4C, especially the compaction and sintering improvement of B4C by applying a Ni-B nanolayer coating on individual B4C particles. A modified electroless coating procedure was proposed and employed to coat nanometer Ni-B layer onto micron-sized B4C particles. The thickness was able to be tuned and controlled below 100 nm. Key parameters, including the amount of nickel source, the amount of the surface activation agent (PdCl2), the amount of the complexing agent (C2H8N2), and the addition rate of the reducing agent (NaBH4) were studied. When the targeted thickness was 5 nm, a continuous and uniform nanolayer coating was obtained with the optimal condition of individual parameter combined. Reduction of the as-coated B4C powder in a H2-Ar atmosphere was studied between 400-900ºC to reduce the surface oxidesâ Ni2O3 and B2O3. Reduction at 800ºC in hydrogen atmosphere was found to be the most effective condition to remove oxygen in the coating layer, with Ni2B as the reduction product. Compaction of the as-received, separated and uncoated, and separated with Ni-B coating B4C powders using uniaxial die compaction and combustion driven compaction (CDC) techniques was studied. CDC technique showed the advantage over the traditional uniaxial die compaction by yielding much higher green density and green strength (73% vs. 53.8% green density for the Ni-B coated B4C). Among compacts obtained from the same technique, Ni-B coated B4C compact yielded the densest packing with crack-free compact surface and the highest strength, demonstrating more bonding between B4C particles provided by Ni-B surface coating. Sintering of the Ni-B coated B4C in an Ar atmosphere between 1150 - 1600ºC with soaking time of 2 hrs and 10 hrs was studied. Liquid phase was found to form during the sintering process. Density measurement showed that the liquid phase Ni-B formed greatly facilitated B4C densification. Considerable density increase and inter-granular connection was achieved when sintered at 1600ºC for 10 hrs. The density enhancement by Ni-B coating was supported by transmission electron microscopy-energy dispersive spectroscopy (TEM-EDS) examination which showed that there was B4C species diffusion into liquid Ni-B phase. This liquid phase enhanced the diffusion of B4C species and formed strong bonding between B4C grains by dissolving small B4C particles and sharp edge and corners of B4C particles. Strength test demonstrated that the Ni-B coating dramatically improved the strength of B4C compacts by yielding a much higher strength of the Ni-B coated samples than the uncoated samples (13.97 vs. 1.79 MPa for the uinaxial die compacted samples, 27.03 vs. 2.21 MPa for the CDC samples). Electrical conductivity Ni-B coated B4C samples was also shown to be improved with the electrical resistivity being reduced from infinite for pure B4C samples to 1.8à 10-3 Ω⠢m for the Ni-B coated samples. This research work has shown that with the Ni-B coating, B4C densification can start at a temperature as low as 1600ºC via a liquid phase sintering process.
Ph. D.
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DeGraffenreid, Allison Lynne. "Studies on boron - nitrogen and boron - gadolinium compounds." The Ohio State University, 1995. http://rave.ohiolink.edu/etdc/view?acc_num=osu1294835746.

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Slade, Alexander Mason Electrical Engineering UNSW. "Boron tribromide sourced boron diffusions for silicon solar cells." Awarded by:University of New South Wales. Electrical Engineering, 2005. http://handle.unsw.edu.au/1959.4/21850.

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This thesis undertakes the development, characterization and optimization of boron diffusion for silicon solar cells. Heavy diffusions (sheet resistance < 40 Ohm/square) to form a back surface field, and light diffusions (sheet resistance > 100 Ohm/square) to form oxide-passivated emitters were developed. Test structures and solar cells were fabricated to assess uniformity, lifetime and recombination effects due to the light and heavy boron diffusions. It was found that the growth of a thin ~200 ??, thermal oxide, during stabilization ??? immediately prior to the boron diffusion - was required to maintain high lifetime and reduce surface recombination (reducing the emitter saturation current density) for all boron diffusions. The heavy boron diffusion process was incorporated into the single side buried contact solar cell processing sequence. The solar cells fabricated had both boron diffused and Al/Si alloyed P+ regions for comparison. This research conclusively showed that boron diffused solar cells had significantly higher open circuit voltage compared to Al/Si alloyed devices. Fabrication of n-type solar cells, and their subsequent characterization by overlayed secondary electron image and the electron beam induced current map showed that the Al/Si alloy varied in depth from 5 to 25 micrometers deep. Methodology and characterization for light, oxide-passivated boron diffusions are also presented. This study yielded boron diffused emitters (sheet resistance > 100 Ohm/square) with low emitter saturation current. It was observed that this was possible only when the thermal oxidation after the boron diffusion was minimal, less than 1,000 ??. This was due to the segregation effect of boron with oxide, decreasing the surface concentration that in turn decreased the electric field repulsion of electrons from the surface. Device modelling of n-type solar cells is presented where the parameters of the modelling include the results of the light, oxide-passivated boron diffusions. This modelling shows n-type-base material with light oxide-passivated boron diffusion has higher potential conversion efficiency than forming a solar cell from phosphorous diffused p-type material.
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Yamamoto, Akihiko. "Boron-based organic reactions using boron cyanides and chlorides." 京都大学 (Kyoto University), 2006. http://hdl.handle.net/2433/143990.

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Kyoto University (京都大学)
0048
新制・課程博士
博士(工学)
甲第12293号
工博第2622号
新制||工||1370(附属図書館)
24129
UT51-2006-N978
京都大学大学院工学研究科合成・生物化学専攻
(主査)教授 杉野目 道紀, 教授 檜山 爲次郎, 教授 村上 正浩
学位規則第4条第1項該当
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Spivack, Arthur J. "Boron isotope geochemistry." Thesis, Massachusetts Institute of Technology, 1986. http://hdl.handle.net/1721.1/15187.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Earth, Atmospheric, and Planetary Sciences, and Woods Hole Oceanographic Institution, 1986.
MICROFICHE COPY AVAILABLE IN ARCHIVES AND LINDGREN
Vita.
Includes bibliographies.
by Arthur J. Spivack.
Ph.D.
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Castro, Susana Patricia. "CHARACTERIZATION OF THE BORON DOPING PROCESSUSING BORON NITRIDE SOLID SOURCE DIFFUSION." NCSU, 1999. http://www.lib.ncsu.edu/theses/available/etd-19990523-142337.

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CASTRO, SUSANA PATRICIA. Characterization of the Boron Doping Process UsingBoron Nitride Solid Source DiffusionThe purpose of this research has been to develop an optimum process for the borondoping of implants and polysilicon gates of metal-oxide-semiconductor (MOS) devices.An experimental design was constructed to determine the effects of diffusiontemperature, time, and ambient on characteristics of the doping process. A temperaturerange of 800 to 1000 degrees Celsius was studied with a diffusion time between 10 and60 minutes. Two diffusion ambients were used for doping processes, a pure nitrogenambient and a nitrogen-oxygen gaseous mixture. Device wafers were fabricated, and thetesting of MOS capacitors and van der Pauw test structures was performed to determinethe effect of diffusion conditions on flatband voltage and poly gate doping. Materialscharacterization techniques were used on monitor wafers for each diffusion process todetermine the wafer structure formed for each process and evaluate the effectiveness ofthe deglaze etch. The processes that resulted in the best device characteristics withoutsuffering from significant poly depletion effects and flatband voltage shifts were wafersdoped at 800 degrees Celsius in a pure nitrogen atmosphere for 20 minutes and 45minutes. The presence of oxygen in the atmosphere caused the depletion of boron fromthe Si wafer surface. The formation of the Si-B phase only occurred on devices processedat 1000 degrees Celsius. The deglaze process used in this experiment did not fullyremove this layer, and thus all devices doped at this temperature were seriously degraded.

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Leenhouts, James Merrell 1968. "Behavior of boron and boron isotopes during uptake by Atriplex canescens." Diss., The University of Arizona, 2000. http://hdl.handle.net/10150/284177.

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This research was conducted to determine the potential for using plants to obtain samples of boron isotopes from groundwater, sod moisture and fracture water. In essence, this work sought to ascertain whether plants can function as in-situ samplers for boron as an environmental isotope. At present, very little is known about the behavior of boron isotopes in plants so this study was designed to reveal any isotopic fractionation that might occur during plant uptake by a specific species under carefully controlled conditions. The relationship between the boron isotope ratios sequestered in the leaves of the species Atriplex canescens and the growth conditions of the plant were investigated using a semi-hydroponic greenhouse experiment. Nutrient boron concentration and solution pH were selected as experimental variables as these parameters span large ranges in nature. In addition, the mechanism through which plants take up anionic nutrients suggests that boron isotope fractionation could occur. The experimental setup was a randomized factorial block design and the plants were provided six different nutrient solutions with pH values ranging from 7.5 to 9.5 and boron concentrations varying from 0.1 mg/L to 10.0 mg/L. Boron concentration in the plant's leaf and stem samples followed expected patterns, with the highest boron amount in the leaves of the plants fed nutrient solution with 10.0 mg/L B. The stern samples of plants fed 0.1 mg/L B contained the least boron. The ratio of boron in plants fed 10.0 mg/L vs. 0.1 mg/L B was far less than the 100:1 ratio of boron in the nutrients, which implies that a component of uptake is actively controlled by the plant. Negative thermal ionization mass spectrometry was employed to analyze the minute amounts of boron extracted from digests of the plant tissues. Statistical tests were utilized to determine that, contrary to the hypothesis, no significant isotopic fractionation occurred during uptake at any treatment pH level. The results of this research indicate that the species Atriplex canescens can provide samples of boron isotopes which closely represent the isotopic signature of the plant's water source.
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Noguchi, Hiroyoshi. "Boron-based organic synthesis through reactivity control by substituents on boron." 京都大学 (Kyoto University), 2008. http://hdl.handle.net/2433/136275.

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Chung, Yoonsun. "Radiobiological evaluation of new boron delivery agents for boron neutron capture therapy." Thesis, Massachusetts Institute of Technology, 2008. http://hdl.handle.net/1721.1/44784.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Nuclear Science and Engineering, 2008.
Includes bibliographical references (p. 123-132).
This thesis evaluates the radiobiological effectiveness of three new boron compounds namely a boronated porphyrin (BOPP) and two liposome formulations for neutron capture therapy (BNCT). The methodology utilizes in vitro and in vivo comparisons that characterize compounds relative to boric acid and boronophenylalanine (BPA). In vitro evaluations utilized a colorimetric assay and 96-well plates to minimize the quantities of compound required for testing. The assay was optimized for the murine SCCVII, squamous cell carcinoma to determine the chemical toxicity and relative cellular uptake of a compound. BOPP was toxic at low concentrations and comparisons between the different compounds for thermal neutron irradiations were performed with approximately 5 [mu]g 10B/ml in the culture medium to allow radiation induced effects to govern the observed response. Using less than 300 [mu]g of compound and 250 kVp X-rays as control irradiations, a compound biological effectiveness (CBE) of 3.3 ± 0.7 was determined for BOPP that is comparable to the result for boric acid (3.5 ± 0.5) indicating a non-selective intracellular accumulation of 10B. BPA has a significantly higher CBE of 6.1 + 0.7. Boronated liposomes (MAC-16 and MAC+TAC) were evaluated with the EMT-6 murine mammary carcinoma. Biodistribution studies showed high 10B uptake in tumor (20-40 [mu]g 10B/g) 30 hours after a single i.v. injection (dose 6-20 [mu]g 10B per gram of body weight). Tumor control experiments were performed using thermal neutrons to study the efficacy of the boron delivered by liposomes and BPA. The MAC-16 produced a 16 % tumor control and BPA (dose 43 [mu]g 10B/gbw) 63 % for tumor boron concentrations of approximately 20 [mu]g 10B/g and the same neutron fluence.
(cont.) Liposome doses were limited by injection volume and so two injections were tried 2-hours apart that doubled the boron concentration in tumor compared to a single administration. This improved the therapeutic response to 67 % with less apparent skin damage than with BPA. Microscopic studies using fluorescent labeled liposomes revealed 10B was nonuniformly distributed and concentrated at the edge of the tumor. Based on these studies in the tumor cell lines chosen neither of the compounds appear superior to BPA.
by Yoonsun Chung.
Ph.D.
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Books on the topic "Boron"

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Boron. New York: Marshall Cavendish Benchmark, 2005.

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Li, Meng, John S. Fossey, and Tony D. James, eds. Boron. Cambridge: Royal Society of Chemistry, 2015. http://dx.doi.org/10.1039/9781782622123.

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Hnyk, Drahomír, and Michael McKee, eds. Boron. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-22282-0.

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C, Smallwood, WHO Task Group on Environmental Health Criteria for Boron., United Nations Environment Programme, International Labour Organisation, World Health Organization, Inter-Organization Programme for the Sound Management of Chemicals., and International Program on Chemical Safety., eds. Boron. Geneva: World Health Organization, 1998.

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Marschall, Horst, and Gavin Foster, eds. Boron Isotopes. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-64666-4.

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Pratt, Barbara J. Around Boron. San Francisco, CA: Arcadia Pub., 2009.

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Pratt, Barbara J. Around Boron. San Francisco, CA: Arcadia Pub., 2009.

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Mukhopadhyay, Falguni. Boron Mala. Calcutta: Swapan Bashak, 1998.

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Pratt, Barbara J. Around Boron. San Francisco, CA: Arcadia Pub., 2009.

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Boboev, Ḣabibullo. Naqshi boron. Khujand: Khuroson, 2018.

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Book chapters on the topic "Boron"

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Lécuyer, Christophe. "Boron." In Encyclopedia of Earth Sciences Series, 1–6. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-39193-9_253-1.

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Lécuyer, Christophe. "Boron." In Encyclopedia of Earth Sciences Series, 156–61. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-39312-4_253.

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Crowson, Phillip. "Boron." In Minerals Handbook 1992–93, 50–55. London: Palgrave Macmillan UK, 1992. http://dx.doi.org/10.1007/978-1-349-12564-7_8.

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Johnson, Giffe T. "Boron." In Hamilton & Hardy's Industrial Toxicology, 79–84. Hoboken, New Jersey: John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781118834015.ch11.

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Crowson, Phillip. "Boron." In Minerals Handbook 1994–95, 50–55. London: Palgrave Macmillan UK, 1994. http://dx.doi.org/10.1007/978-1-349-13431-1_8.

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Crowson, Phillip. "Boron." In Minerals Handbook 1996–97, 64–70. London: Palgrave Macmillan UK, 1996. http://dx.doi.org/10.1007/978-1-349-13793-0_8.

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Brookins, Douglas G. "Boron." In Eh-pH Diagrams for Geochemistry, 44–45. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73093-1_17.

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Keren, R. "Boron." In SSSA Book Series, 603–26. Madison, WI, USA: Soil Science Society of America, American Society of Agronomy, 2018. http://dx.doi.org/10.2136/sssabookser5.3.c21.

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Moore, Jame W. "Boron." In Springer Series on Environmental Management, 57–63. New York, NY: Springer New York, 1991. http://dx.doi.org/10.1007/978-1-4612-3004-5_7.

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Kennedy, John D. "Boron." In Multinuclear NMR, 221–58. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1783-8_8.

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Conference papers on the topic "Boron"

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Bullett, D. W. "The electronic origin disorder in boron and boron-rich borides." In Boron-rich solids. AIP, 1991. http://dx.doi.org/10.1063/1.40874.

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Papandreou, N., and L. Zuppiroli. "Low temperature ac electrical properties of boron carbide." In Boron-rich solids. AIP, 1991. http://dx.doi.org/10.1063/1.40806.

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Tanaka, T., and Y. Ishizawa. "The electron Fermi surface of HfB2." In Boron-rich solids. AIP, 1991. http://dx.doi.org/10.1063/1.40820.

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Kharlamov, A. I., and S. V. Loichenko. "Investigation: The process of densitification of boron-rich compounds of the Al-B-C system." In Boron-rich solids. AIP, 1991. http://dx.doi.org/10.1063/1.40821.

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Kryuk, V. I., and E. A. Knyshev. "Exoemission properties of turbostratic boron nitride." In Boron-rich solids. AIP, 1991. http://dx.doi.org/10.1063/1.40795.

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Vepr̆ek, S. "Boron carbide large area in-situ coatings for controlled nuclear fusion research." In Boron-rich solids. AIP, 1991. http://dx.doi.org/10.1063/1.40796.

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Belitskus, D. L., R. J. Campbell, and S. Y. Tzeng. "Effects of reaction parameters on boron carbide powder production by the carbothermic process." In Boron-rich solids. AIP, 1991. http://dx.doi.org/10.1063/1.40822.

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Tsagareishvili, D. Sh, M. Ch Tushishvili, and G. V. Tsagareishvili. "Estimation of some thermoelastic properties of boron suboxide in wide ranges of temperature." In Boron-rich solids. AIP, 1991. http://dx.doi.org/10.1063/1.40858.

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Abel’skii, Sh Sh. "Low temperature anomaly of boron nitride heat capacity." In Boron-rich solids. AIP, 1991. http://dx.doi.org/10.1063/1.40859.

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Tardy, Herbert L., Terrence L. Aselage, and David Emin. "Dielectric function of boron carbides from Kramers-Kronig analysis of reflectance spectra." In Boron-rich solids. AIP, 1991. http://dx.doi.org/10.1063/1.40886.

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Reports on the topic "Boron"

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Agarwal, A., D. J. Eaglesham, H. J. Gossmann, L. Pelaz, S. B. Herner, D. C. Jacobson, T. E. Haynes, and Y. E. Erokhin. Boron-enhanced diffusion of boron from ultralow-energy boron implantation. Office of Scientific and Technical Information (OSTI), May 1998. http://dx.doi.org/10.2172/650277.

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Baker, I., X. Li, H. Xiao, O. Klein, C. Nelson, R. L. Carleton, and E. P. George. Boron strengthening in FeAl. Office of Scientific and Technical Information (OSTI), November 1998. http://dx.doi.org/10.2172/676870.

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Bell, Z. W., L. Maya, G. M. Brown, and F. V. Jr Sloop. Boron-Loaded Silicone Rubber Scintillators. Office of Scientific and Technical Information (OSTI), May 2003. http://dx.doi.org/10.2172/812578.

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Kouzes, Richard T., James H. Ely, Azaree T. Lintereur, and Edward R. Siciliano. Boron-10 ABUNCL Active Testing. Office of Scientific and Technical Information (OSTI), July 2013. http://dx.doi.org/10.2172/1089083.

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Geist, William H., Daniela Henzlova, and Howard Olsen Menlove. Boron-lined parallel-plate Collar. Office of Scientific and Technical Information (OSTI), September 2016. http://dx.doi.org/10.2172/1329605.

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Nelson, H. H. NRL Boron Propellants Combustion Program. Fort Belvoir, VA: Defense Technical Information Center, June 1988. http://dx.doi.org/10.21236/ada201242.

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Nelson, H. H. Reaction Chemistry of Boron Hydrides. Fort Belvoir, VA: Defense Technical Information Center, May 1988. http://dx.doi.org/10.21236/ada201243.

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Lintereur, Azaree T., Richard T. Kouzes, James H. Ely, Luke E. Erikson, and Edward R. Siciliano. Boron-Lined Neutron Detector Measurements. Office of Scientific and Technical Information (OSTI), November 2009. http://dx.doi.org/10.2172/968479.

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Lintereur, Azaree T., Richard T. Kouzes, James H. Ely, Luke E. Erikson, Edward R. Siciliano, and Mitchell L. Woodring. Boron-Lined Neutron Detector Measurements. Office of Scientific and Technical Information (OSTI), March 2010. http://dx.doi.org/10.2172/973979.

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Chatterjee, Tapan, Stacey Kerwien, and Elias Jelis. Microstructure Analysis of Boron Nitride. Fort Belvoir, VA: Defense Technical Information Center, September 2009. http://dx.doi.org/10.21236/ada505516.

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