JPH1060730A - フィブリドの製造方法及びポリアリーレンエーテルフィブリド - Google Patents

フィブリドの製造方法及びポリアリーレンエーテルフィブリド

Info

Publication number: JPH1060730A
Authority: JP; Japan
Prior art keywords: solution; fibrid; fibrids; polyarylene ether; coagulation medium
Prior art date: 1996-05-07
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Withdrawn

Application number

JP11541097A

Other languages

English (en)

Japanese (ja)

Inventor

Heinz Berbner

ベルプナーハインツ

Ulrich Dr Eichenauer

アイヒェナウアーウルリッヒ

Juergen Goepel

ゲーペルユルゲン

Eckhard Neufeld

ノイフェルトエックハルト

Hans Dieter Zettler

ディーターツェットラーハンス

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

BASF SE

Original Assignee

BASF SE

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1996-05-07

Filing date

1997-05-06

Publication date

1998-03-03

1997-05-06 Application filed by BASF SE filed Critical BASF SE

1998-03-03 Publication of JPH1060730A publication Critical patent/JPH1060730A/ja

Status Withdrawn legal-status Critical Current

Links

RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 title claims abstract description 70
229920000412 polyarylene Polymers 0.000 title claims abstract description 43
238000004519 manufacturing process Methods 0.000 title claims description 10
239000007788 liquid Substances 0.000 claims abstract description 22
239000003960 organic solvent Substances 0.000 claims abstract description 15
238000010008 shearing Methods 0.000 claims abstract description 9
230000015271 coagulation Effects 0.000 claims description 46
238000005345 coagulation Methods 0.000 claims description 46
230000015572 biosynthetic process Effects 0.000 claims description 12
238000000034 method Methods 0.000 abstract description 36
229920000642 polymer Polymers 0.000 abstract description 27
-1 ether sulfone Chemical class 0.000 abstract description 17
239000002904 solvent Substances 0.000 abstract description 16
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 abstract description 10
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract description 8
239000000243 solution Substances 0.000 description 44
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
229920001577 copolymer Polymers 0.000 description 11
239000000203 mixture Substances 0.000 description 8
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 7
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
150000002170 ethers Chemical class 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
239000000725 suspension Substances 0.000 description 5
125000004432 carbon atom Chemical group C* 0.000 description 4
230000001112 coagulating effect Effects 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
239000000835 fiber Substances 0.000 description 4
239000000463 material Substances 0.000 description 4
238000002156 mixing Methods 0.000 description 4
239000002245 particle Substances 0.000 description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
125000001424 substituent group Chemical group 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
239000004695 Polyether sulfone Substances 0.000 description 3
239000007900 aqueous suspension Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
229910052739 hydrogen Inorganic materials 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
150000002576 ketones Chemical class 0.000 description 3
230000002093 peripheral effect Effects 0.000 description 3
229920006393 polyether sulfone Polymers 0.000 description 3
229920005989 resin Polymers 0.000 description 3
239000011347 resin Substances 0.000 description 3
238000007711 solidification Methods 0.000 description 3
230000008023 solidification Effects 0.000 description 3
230000003068 static effect Effects 0.000 description 3
239000000126 substance Substances 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
229920003043 Cellulose fiber Polymers 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
239000004698 Polyethylene Substances 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
125000000753 cycloalkyl group Chemical group 0.000 description 2
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
GUVUOGQBMYCBQP-UHFFFAOYSA-N dmpu Chemical class CN1CCCN(C)C1=O GUVUOGQBMYCBQP-UHFFFAOYSA-N 0.000 description 2
239000002657 fibrous material Substances 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
125000001624 naphthyl group Chemical group 0.000 description 2
239000004745 nonwoven fabric Substances 0.000 description 2
239000004417 polycarbonate Substances 0.000 description 2
229920000515 polycarbonate Polymers 0.000 description 2
229920000728 polyester Polymers 0.000 description 2
229920000573 polyethylene Polymers 0.000 description 2
229920000098 polyolefin Polymers 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
238000012545 processing Methods 0.000 description 2
238000005086 pumping Methods 0.000 description 2
229920001059 synthetic polymer Polymers 0.000 description 2
238000012360 testing method Methods 0.000 description 2
238000005406 washing Methods 0.000 description 2
125000000027 (C1-C10) alkoxy group Chemical group 0.000 description 1
MIZLGWKEZAPEFJ-UHFFFAOYSA-N 1,1,2-trifluoroethene Chemical group FC=C(F)F MIZLGWKEZAPEFJ-UHFFFAOYSA-N 0.000 description 1
BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
239000004705 High-molecular-weight polyethylene Substances 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004642 Polyimide Substances 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
229920001328 Polyvinylidene chloride Polymers 0.000 description 1
229910004298 SiO 2 Inorganic materials 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
230000001133 acceleration Effects 0.000 description 1
125000002723 alicyclic group Chemical group 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
206010061592 cardiac fibrillation Diseases 0.000 description 1
238000005119 centrifugation Methods 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
239000000701 coagulant Substances 0.000 description 1
230000001427 coherent effect Effects 0.000 description 1
238000011437 continuous method Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000005520 cutting process Methods 0.000 description 1
150000004292 cyclic ethers Chemical class 0.000 description 1
229940117389 dichlorobenzene Drugs 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
238000001493 electron microscopy Methods 0.000 description 1
238000005265 energy consumption Methods 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
239000004744 fabric Substances 0.000 description 1
230000002600 fibrillogenic effect Effects 0.000 description 1
239000000945 filler Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
229920005570 flexible polymer Polymers 0.000 description 1
150000002240 furans Chemical class 0.000 description 1
238000000227 grinding Methods 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
239000008240 homogeneous mixture Substances 0.000 description 1
238000000265 homogenisation Methods 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
230000002209 hydrophobic effect Effects 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000012452 mother liquor Substances 0.000 description 1
238000000465 moulding Methods 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920001601 polyetherimide Polymers 0.000 description 1
229920001721 polyimide Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000005033 polyvinylidene chloride Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000011084 recovery Methods 0.000 description 1
230000003014 reinforcing effect Effects 0.000 description 1
238000012216 screening Methods 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000009987 spinning Methods 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 description 1
238000011144 upstream manufacturing Methods 0.000 description 1
238000005303 weighing Methods 0.000 description 1
238000003466 welding Methods 0.000 description 1

Classifications

- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/66—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyethers
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/40—Formation of filaments, threads, or the like by applying a shearing force to a dispersion or solution of filament formable polymers, e.g. by stirring

Landscapes

Engineering & Computer Science (AREA)
Chemical & Material Sciences (AREA)
Textile Engineering (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Dispersion Chemistry (AREA)
Mechanical Engineering (AREA)
Artificial Filaments (AREA)
Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
Paper (AREA)

JP11541097A 1996-05-07 1997-05-06 フィブリドの製造方法及びポリアリーレンエーテルフィブリド Withdrawn JPH1060730A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE1996118330 DE19618330A1 (de)	1996-05-07	1996-05-07	Verfahren zur Herstellung von Fibrillen
DE19618330.8		1996-05-07

Publications (1)

Publication Number	Publication Date
JPH1060730A true JPH1060730A (ja)	1998-03-03

Family

ID=7793607

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP11541097A Withdrawn JPH1060730A (ja)	1996-05-07	1997-05-06	フィブリドの製造方法及びポリアリーレンエーテルフィブリド

Country Status (3)

Country	Link
EP (1)	EP0806500A1 (fr)
JP (1)	JPH1060730A (fr)
DE (1)	DE19618330A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2006225807A (ja) *	2005-02-18	2006-08-31	Toray Ind Inc	パルプおよびその製造方法ならびにペーパー、電気絶縁材料

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US10119214B2 (en)	2013-07-17	2018-11-06	Sabic Global Technologies B.V.	Force spun sub-micron fiber and applications
JP2016528401A (ja)	2013-08-15	2016-09-15	サビックグローバルテクノロジーズベスローテンフェンノートシャップ	剪断紡糸されたサブマイクロメートル繊維

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE795724A (fr) *	1972-02-25	1973-08-21	Basf Ag	Procede et dispositif de fabrication de fibres courtes en matieres synthetiques thermoplastiques
DE2543824C3 (de) *	1975-10-01	1980-05-14	Basf Ag, 6700 Ludwigshafen	Verfahren zur Herstellung von Fibrillen aus Poly(amid-imid)-harzen und die Fibrillen aus diesen Harzen
JPS52121524A (en) *	1976-04-06	1977-10-13	Teijin Ltd	Production of pulp like substance
JPS52124904A (en) *	1976-04-12	1977-10-20	Teijin Ltd	Process for making sheets
DE2646332B2 (de) *	1976-10-14	1979-04-12	Basf Ag, 6700 Ludwigshafen	Verfahren zur Herstellung von Fibrillen aus fluorhaltigen Polymerisaten
EP0790852A1 (fr) *	1994-11-08	1997-08-27	Hoechst Aktiengesellschaft	Materiau de filtration et procede d'elimination de composants de melanges gazeux et de liquides

1996
- 1996-05-07 DE DE1996118330 patent/DE19618330A1/de not_active Withdrawn
1997
- 1997-05-05 EP EP97107360A patent/EP0806500A1/fr not_active Ceased
- 1997-05-06 JP JP11541097A patent/JPH1060730A/ja not_active Withdrawn

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2006225807A (ja) *	2005-02-18	2006-08-31	Toray Ind Inc	パルプおよびその製造方法ならびにペーパー、電気絶縁材料

Also Published As

Publication number	Publication date
DE19618330A1 (de)	1997-11-13
EP0806500A1 (fr)	1997-11-12

Legal Events

Date

Code

Title

Description

2004-07-06

A300

Withdrawal of application because of no request for examination

Free format text: JAPANESE INTERMEDIATE CODE: A300

Effective date: 20040706

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US4091058A (en)	1978-05-23	Manufacture of fibrids from poly(amide-imide) resins
US4219512A (en)	1980-08-26	Manufacture of fibrids from polymers
AU757068B2 (en)	2003-01-30	Process and apparatus for producing fibrets from cellulose derivatives
CN1241224A (zh)	2000-01-12	聚(四氟乙烯)及相关聚合物的分散体纺丝法
US4187143A (en)	1980-02-05	Manufacture of fibrids from poly(amide-imide) resins
US4224259A (en)	1980-09-23	Manufacture of fibrids from polymers
JPH1060730A (ja)	1998-03-03	フィブリドの製造方法及びポリアリーレンエーテルフィブリド
JPS58203118A (ja)	1983-11-26	紙ないし非紙分野におけるセルロ−ス繊維の代替に適した二成分合成繊維とその製造方法
EP0103398A2 (fr)	1984-03-21	Fibres cellulosiques à partir de solutions anisotropes
CN108623697B (zh)	2021-10-08	羟丙基甲基纤维素的生产方法
DE2543816C3 (de)	1980-09-25	Verwendung von Fibrillen aus aromatischen Poly(amid-imid)harzen zur Herstellung von papier- und textilähnlichen Flächengebilden
US20240183079A1 (en)	2024-06-06	Process to manufacture an aramid solution
EP0192454B1 (fr)	1990-05-02	Procédé de préparation de fibres cellulosiques de haute ténacité
JP5110338B2 (ja)	2012-12-26	ポリアミドとガラスとの複合体から成るパルプと粒子の製造法
US2858304A (en)	1958-10-28	Alkali cellulose aging
JPH0819633B2 (ja)	1996-02-28	剛直鎖芳香族ポリアミド繊維安定化懸濁液の製造方法
NO133815B (fr)	1976-03-22
JPH07150474A (ja)	1995-06-13	セルロ−スシ−トの製造方法

JPH1060730A - フィブリドの製造方法及びポリアリーレンエーテルフィブリド - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (2)

Publications (1)

Family

ID=7793607

Family Applications (1)

Country Status (3)

Cited By (1)

Families Citing this family (2)

Family Cites Families (6)

Cited By (1)

Also Published As

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