manifestation_id	original_title	title_alternative	title_transcription	statement_of_responsibility	manifestation_identifier	creator	contributor	publisher	date_of_publication	pub_date	year_of_publication	publication_place	manifestation_created_at	manifestation_updated_at	carrier_type	content_type	frequency	language	isbn	issn	doi	jpno	ncid	lccn	iss_itemno	volume_number	volume_number_string	edition	edition_string	issue_number	issue_number_string	serial_number	extent	start_page	end_page	dimensions	height	width	depth	manifestation_price	access_address	manifestation_required_role	abstract	description	identifier:unknown	identifier:nbn	identifier:isbn10	identifier:iss_itemno	identifier:online_isbn	identifier:print_isbn	identifier:print_issn	identifier:online_issn	identifier:escidoc	identifier:nims	series_statement_id	series_statement_original_title	series_statement_title_subseries	series_statement_title_subseries_transcription	series_statement_title_transcription	series_statement_creator	series_statement_volume_number	series_statement_series_master	series_statement_root_manifestation_id	series_statement_manifestation_id	series_statement_position	series_statement_note	series_statement_created_at	series_statement_updated_at	subject:ndlsh	subject:unknown	subject:bsh	classification:ndc8	classification:ndc9	classification:udc	item_id	item_identifier	binding_item_identifier	call_number	library	shelf	item_note	accepted_at	acquired_at	item_created_at	item_updated_at
103296	ファイバフューズの伝搬挙動					""	""	""	2010-08-31 00:00:00 +0900	2010-08-31	2010		2015-05-28 18:03:07 +0900	2023-07-31 14:13:13 +0900	online_resource	text	unknown	Japanese	""	""																					https://hdl.handle.net/20.500.11932/513183	Guest	1987年に発見されたファイバフューズ現象に関する研究発表数が増加しはじめたのは2003年。今年3月にはOITDA規格技術資料が発行されるまでになった。本報告ではこれを補足する内容を述べる。ファイバフューズのマクロな伝搬挙動は、散逸ソリトンとして理解することができる。そこでは、伝搬光からのエネルギーを光と熱に変換する非可逆反応が起きており、この入出力のバランスを崩すことが、ファイバフューズ停止技術につながる。周期的空孔列とプラズマ内に誘起される不安定性との関係を超高速撮影映像に基づいて検討した。生成した空孔が押しつぶされるプロセスは、プラズマ末尾の変調された発光が消えた後に起こっていることが分かった。 		""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	fiber fuse//optical fiber//dissipative soliton//in situ observation//fiber fuse//optical fiber//dissipative soliton//in situ observation//fiber fuse//optical fiber//dissipative soliton//in situ observation	""	""	""	""	94565				web	web				2023-07-31 14:13:13 +0900	2023-07-31 14:13:13 +0900
103292	SAMURI Project: NIMS eSciDoc Digital Library					""	""	""	2010-11-16 00:00:00 +0900	2010-11-16	2010		2015-05-28 18:03:06 +0900	2023-07-31 14:16:19 +0900	online_resource	text	unknown	unknown	""	""																					https://hdl.handle.net/20.500.11932/541570	Guest			""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	researchers directory//SAMURAI//eScience//eSciDoc//researchers directory//SAMURAI//eScience//eSciDoc//researchers directory//SAMURAI//eScience//eSciDoc	""	""	""	""	95158				web	web				2023-07-31 14:16:19 +0900	2023-07-31 14:16:19 +0900
103293	Collaboration of Scholarly Communication -Advancing libraries in Japan					""	""	""	2010-11-09 00:00:00 +0900	2010-11-09	2010		2015-05-28 18:03:06 +0900	2023-07-31 14:15:02 +0900	online_resource	text	unknown	unknown	""	""																					https://hdl.handle.net/20.500.11932/541609	Guest			""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	Scholarly Communication//library roles//digital era//collaboration//world standard format//protocol//digital library//NIMS eSciDoc//Scholarly Communication//library roles//digital era//collaboration//world standard format//protocol//digital library//NIMS eSciDoc//Scholarly Communication//library roles//digital era//collaboration//world standard format//protocol//digital library//NIMS eSciDoc	""	""	""	""	94911				web	web				2023-07-31 14:15:02 +0900	2023-07-31 14:15:02 +0900
103290	E-Science Experiences at NIMS eSciDoc : Self Archiving of Profiled Experimental Data					""	""	""	2009-12-03 00:00:00 +0900	2009-12-03	2009		2015-05-28 18:03:05 +0900	2023-07-31 14:12:47 +0900	online_resource	text	unknown	unknown	""	""																					https://hdl.handle.net/20.500.11932/239877	Guest			""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	94482				web	web				2023-07-31 14:12:47 +0900	2023-07-31 14:12:47 +0900
103291	View from the front line: what do librarians want?					""	""	""	2010-02-03 00:00:00 +0900	2010-02-03	2010		2015-05-28 18:03:05 +0900	2023-07-31 14:45:08 +0900	online_resource	text	unknown	unknown	""	""																					https://hdl.handle.net/20.500.11932/239880	Guest			""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	100530				web	web				2023-07-31 14:45:08 +0900	2023-07-31 14:45:08 +0900
103289	Floating-zone crystal growth of Nb-doped YB66 for soft X-ray monochromator use					""	""	""	2004-12-15 00:00:00 +0900	2004-12-15	2004		2015-05-28 18:03:04 +0900	2023-07-31 14:40:56 +0900	online_resource	text	unknown	unknown	""	""														0	0						https://hdl.handle.net/20.500.11932/458235	Guest	Nb-doped YB66 single crystals were grown by the floating zone method using a 4 ellipsoidal mirror-type xenon lamp image furnace. Nb-doping is expected to improve the performance of YB66 soft X-ray monochromators. Maximum site occupancy of Nb achieved was 95%. Full-width at half-maximum of the rocking curve measured for CuKα 10 0 0 reflection achieved 40–50 arcsec. Thermal conductivity of the crystal with the maximum site occupancy increased about two times that of undoped YB66 crystals.		""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	Doping; Floating-zone technique; Borides; Soft X-ray monochromator materials//Doping; Floating-zone technique; Borides; Soft X-ray monochromator materials//Doping; Floating-zone technique; Borides; Soft X-ray monochromator materials	""	""	""	""	99741				web	web				2023-07-31 14:40:56 +0900	2023-07-31 14:40:56 +0900
103287	Novel ternary Y-B-C compound: Y10+xB7C10-x (x ≈ 0.1)					""	""	""	2009-07-24 00:00:00 +0900	2009-07-24	2009		2015-05-28 18:03:03 +0900	2023-07-31 14:56:28 +0900	online_resource	text	unknown	unknown	""	""														12006							https://hdl.handle.net/20.500.11932/458237	Guest	A novel ternary Y-B-C compound Y10+xB7C10−x is established. Y10+xB7C10−x has a monoclinic crystal structure with space group C2/c (No.15) and lattice constants a = 1.1273(14) nm, b = 1.1159(14) nm, c = 2.3566(30) nm and beta = 98.15(2) . Y10+xB7C10−x crystal rods were grown by floating zone technique and consisted of a predominant crystal phase and impurity phases. A small crystal having sufficient quality for single crystal XRD analysis could be selected. Structure refinement achieved a final R1 = 0.044 for 1660 independent reflections with Fo > 4 (Fo). 10 Y sites, 8 B sites, 9 C sites and one C/Y mixed occupancy site with about 0.9/0.1 occupation ratio were assigned. The unit chemical formula is Y10+xB7C10−x (x 0.1), and the unit cell contains 8 formula units. Y10+xB7C10−x has a layer structure: Y-C double layers, in which Y and C bond alternatively like in the NaCl structure, spread parallel to the (001) plane and stack along the c-axis. The Y-C double layer is connected to the neighboring Y-C double layers via C-B-C chains or C-B-B-C chains. This structure was confirmed by electron diffraction and high-resolution electron microscopy. Magnetic susceptibility measurement indicated that the Y10+xB7C10−x phase has no superconductivity above 2 K. A minor superconducting phase with Tc=7.5 K was observed, but ascribed to an unidentified impurity phase.		""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	ternary Y-B-C compound//Y10+xB7C10−x//single crystal XRD//structure determination//ternary Y-B-C compound//Y10+xB7C10−x//single crystal XRD//structure determination//ternary Y-B-C compound//Y10+xB7C10−x//single crystal XRD//structure determination	""	""	""	""	102629				web	web				2023-07-31 14:56:28 +0900	2023-07-31 14:56:28 +0900
103288	Structure refinement of quaternary RE-B-C-Si compounds: Y3−x(B12)3(CSi)Si8 (x ≈ 0.96) and Dy3−x(B12)3(CSi)Si8 (x ≈ 0.90)					""	""	""	2009-07-24 00:00:00 +0900	2009-07-24	2009		2015-05-28 18:03:03 +0900	2023-07-31 14:19:51 +0900	online_resource	text	unknown	unknown	""	""														12015							https://hdl.handle.net/20.500.11932/458239	Guest	We refined the crystal structure of quaternary RE-B-C-Si (RE = Y or Dy) compounds Y3-x(B12)3(CSi)Si8 (x ≈ 0.96) and Dy3-x(B12)3(CSi)Si8 (x ≈ 0.90). Both compounds have a trigonal crystal structure with space group Rm (No. 166). They have previously been assigned as ternary RE-B-Si compounds, but we incorporated carbon to the new structure refinements. The refinement for Y3-x(B12)3(CSi)Si8 achieved a final R1 = 0.0288 for 1178 independent reflections with F0 > 4σ(F0) and 0.0431 for all 1484 reflections, and the refinement for Dy3-x(B12)3(CSi)Si8 achieved a final R1= 0.0382 for 2009 independent reflections with F0 > 4σ(F0) and 0.0385 for all 2022 reflections. The new structure refinements suggest the presence of (B12)3-Si-C-(B12)3 units, which, together with two other units, B12 icosahedron cluster and Si8 ethane like cluster, stabilize the RE3-x(B12)3(CSi)Si8 crystal structure.		""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	quaternary RE-B-C-Si compounds//Y3−x(B12)3(CSi)Si8 (x ≈ 0.96)//Dy3−x(B12)3(CSi)Si8 (x ≈ 0.90)//structure refinement//quaternary RE-B-C-Si compounds//Y3−x(B12)3(CSi)Si8 (x ≈ 0.96)//Dy3−x(B12)3(CSi)Si8 (x ≈ 0.90)//structure refinement//quaternary RE-B-C-Si compounds//Y3−x(B12)3(CSi)Si8 (x ≈ 0.96)//Dy3−x(B12)3(CSi)Si8 (x ≈ 0.90)//structure refinement	""	""	""	""	95825				web	web				2023-07-31 14:19:51 +0900	2023-07-31 14:19:51 +0900
103285	Floating Zone Crystal Growth and Structure Analysis of a Novel ScB19 Family Compound, ScB19+xSiy					""	""	""	2002-02-26 00:00:00 +0900	2002-02-26	2002		2015-05-28 18:03:02 +0900	2023-07-31 14:31:06 +0900	online_resource	text	unknown	unknown	""	""														394	400						https://hdl.handle.net/20.500.11932/458051	Guest	Single crystals of a novel ScB19 family compound ScB19+xSiy were grown by the floating zone method using a four-lamp mirror-type image furnace. A small amount of silicon addition to ScB19 which decomposes at elevated temperatures without melting allowed it to coexist with the liquid phase and as a resultant made the floating zone crystal growth possible. Powder X-ray diffraction analysis confirmed the grown crystals of ScB19+xSiy to be isostructural to ScB19. It was found that the crystal structure of ScB19+xSiy solved based on single-crystal X-ray data is tetragonal with lattice constants of a, b=1.03081(2) nm, c=1.42589(3) nm, space group P41212 or P43212 and is basically isotypic with α-AlB12 structure type. In the crystal structure boron atoms form a three-dimensional framework based on interconnected B12 icosahedra and B22 polyhedra. The Sc atoms reside in three of five Al sites in the α-AlB12 structure and Si resides in a bridge site bonding two B22 units.		""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	boron-rich scandium boride; scandium borosilicide; floating zone crystal growth; ScB19+xSiy; ScB19; tetragonal crystal structure; icosahedral boron cluster//boron-rich scandium boride; scandium borosilicide; floating zone crystal growth; ScB19+xSiy; ScB19; tetragonal crystal structure; icosahedral boron cluster//boron-rich scandium boride; scandium borosilicide; floating zone crystal growth; ScB19+xSiy; ScB19; tetragonal crystal structure; icosahedral boron cluster	""	""	""	""	97915				web	web				2023-07-31 14:31:06 +0900	2023-07-31 14:31:06 +0900
103286	eSciDoc Update					""	""	""	2010-07-16 00:00:00 +0900	2010-07-16	2010		2015-05-28 18:03:02 +0900	2023-07-31 14:53:42 +0900	online_resource	text	unknown	English	""	""																					https://hdl.handle.net/20.500.11932/468680	Guest			""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	""	102122				web	web				2023-07-31 14:53:42 +0900	2023-07-31 14:53:42 +0900