CN1765796A - Low-refraction er-doped fluorine phosphorous glass and preparation method thereof - Google Patents
Low-refraction er-doped fluorine phosphorous glass and preparation method thereof Download PDFInfo
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- CN1765796A CN1765796A CN 200510029054 CN200510029054A CN1765796A CN 1765796 A CN1765796 A CN 1765796A CN 200510029054 CN200510029054 CN 200510029054 CN 200510029054 A CN200510029054 A CN 200510029054A CN 1765796 A CN1765796 A CN 1765796A
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Abstract
A kind of low-refraction er-doped fluorine phosphorous glass that is used for evanescent wave optical fiber amplifier and preparation method thereof, it is composed as follows: glass ingredient: mol%; Al (PO
3)
3: 2.5~5; AlF
3: 27~39; MgF
2: 6~10; CaF
2: 19~26; SrF
2: 5~8; BaF
2: 7~10; NaF:0,15~20; KF:0~8; ErF
3: 3~6.
Description
Technical field
The present invention relates to the er-doped fluorine phosphorous glass, er-doped fluorine phosphorous glass of especially a kind of low-refraction that is used for evanescent wave optical fiber amplifier and preparation method thereof.
Background technology
Evanescent wave optical fiber amplifier (Evanescent Wave Fiber Amplifier, be designated hereinafter simply as EWFA), has the initiatively structure of the passive sandwich layer of covering, its noise noise than common erbium doped optic fibre amplifier EDFA (Erbium Doped Fiber Amplifier) little 10000 times (referring to document: A.V.Astakhov, M.M.Butusov, S.L Galkin, Opt.Spectrosc., 59 (1985) 551), thereby be subjected to researchist's attention.
Make EWFA, must on optical fiber, scribe grating, thereby must adopt photosensitivity optical fiber, thereby the specific refractory power that changes optical fiber by uv irradiating obtains grating, and the light-sensitive optical fibre of present technical comparative maturity is a silica fibre of mixing germanium, be subjected to the influence of its quartz substrate, its specific refractory power is lower, and the specific refractory power of 1550nm is greatly in 1450~1.460 scopes.
The refractive index n that is used for the erbium doped-glass of EWFA
GlassAnd the relation between the specific refractory power of photosensitivity optical fiber is as follows: n
Core>n
Effective>n
Glass>n
Bag, n wherein
Core, n
Effective, n
BagBe respectively sandwich layer specific refractory power, effective refractive index and the cladding index of optical fiber.Therefore, have only the erbium doped-glass of employing low-refraction to be complementary with germanium-doped silica fiber.
Because the action length of evanescent wave has only about 2cm, therefore require erbium glass should have high Er
3+Concentration is to realize high as far as possible gain, though traditional silica glass specific refractory power can satisfy the requirement of EWFA, its erbium mixes limited in one's ability.So the laser glass that the development low-refraction has higher erbium doping content simultaneously becomes the important step that realizes the EWFA technology.
People such as Zhang Liyan once reported a kind of high erbium concentration fluorine phosphorous glass of low-refraction (referring to patent: Zhang Liyan, Zhang Junjie, Hu Lili, Sun Hongtao, low-refraction high density er-doped fluorine phosphorous glass and preparation method thereof, number of patent application: 200410017810), but the specific refractory power at its 1550nm place is not suitable for EWFA all greater than 1.460.
Summary of the invention
The invention provides a kind of low-refraction er-doped fluorine phosphorous glass that is used for evanescent wave optical fiber amplifier and preparation method thereof.The transition temperature of this glass is at 425~465 ℃, stability, glass parameter Δ T 〉=80 ℃, refractive index n
dBetween 1.460~1.470, n
1550Between 1.452~1.460, the erbium doping content can reach 6mol%.
Technical solution of the present invention is as follows:
A kind of low-refraction er-doped fluorine phosphorous glass, it is composed as follows:
Glass ingredient molar percentage (mol%)
Al(PO
3)
3 2.5~5
AlF
3 27~39
MgF
2 6~10
CaF
2 19~26
SrF
2 5~8
BaF
2 7~10
NaF 0,15~20
KF 0~8
ErF
3 3~6
The concrete preparation method of low-refraction er-doped fluorine phosphorous glass of the present invention comprises the steps:
1.: the molar percentage of forming by glass (mol%) calculates weight of glass per-cent, takes by weighing raw material then, mixes;
2.: compound is put into corundum crucible, place 950~1020 ℃ silicon carbon rod electric furnace fusion, melting time was controlled at 10~20 minutes;
3.: behind the glass melting, feed the high pure nitrogen homogenizing, what of raw material aeration time be decided by;
4.: stop logical nitrogen, clarified 10~20 minutes, then glass metal is poured in the mould of preheating;
5.: glass is put into be warming up to transition temperature (T fast
g) retort furnace in, be incubated after 4 hours, be cooled to about 300 ℃ with 10 ℃/hour speed, and then be annealed to room temperature with 15 ℃/hour speed.
Differential thermal analysis shows: the transition temperature of low-refraction er-doped fluorine phosphorous glass of the present invention in 420~470 ℃ of scopes, stability, glass parameter Δ T 〉=80 ℃, as shown in Figure 1, the crystallization peak on the differential thermal curve a little less than, show that the crystallization stability of this glass is good.
Adopt the V prism method to record n
f, n
dAnd n
c, adopt Cauchy formula (n=a+b/ λ
2, n represents specific refractory power, a, b are constant, λ represents wavelength) and calculate n
1550N wherein
f, n
d, n
cAnd n
1550Represent the specific refractory power when wavelength is 486.1nm, 589.3nm, 656.3nm and 1550nm respectively.
Description of drawings
Fig. 1 is the differential thermal curve of low-refraction er-doped fluorine phosphorous glass of the present invention.
Embodiment
4 specific embodiments of low-refraction er-doped fluorine phosphorous glass of the present invention are as shown in table 1:
Table 1
Component (mol%) | 1 # | 2 # | 3 # | 4 # |
Al(PO 3) 3 AlF 3 MgF 2 CaF 2 SrF 2 BaF 2 NaF KF ErF 3 T g(℃) | 2.5 39 7 25 7 7.5 0 8 4 425 | 4 38 10 24 8 10 0 0 6 448 | 4 28 7 21 8 9 20 0 3 440 | 5 32 6 20 5 7 16 4 5 465 |
T x(℃) ΔT n d n 1550 | 520 95 1.4604 1.4523 | 565 117 1.4662 1.4586 | 550 110 1.4652 1.4574 | 597 132 1.4701 1.4618 |
Annotate: T
gBe glass transformation temperature, T
xBe the crystallization starting temperature, Δ T=T
x-T
g
Embodiment 1
#:
Form as in the table 11
#Shown in, concrete preparation method comprises the following steps:
1.: press in the table 11
#The molar percentage (mol%) that glass is formed calculates weight of glass per-cent, takes by weighing raw material then, mixes;
2.: compound is put into corundum crucible, place 950 ℃ silicon carbon rod electric furnace fusion;
3.: behind the glass melting, feed the high pure nitrogen homogenizing, what of raw material aeration time be decided by;
4.: stop logical nitrogen, glass metal is protected clarified at 950 ℃, what of raw material its time also depend on, then glass metal poured in the mould of preheating;
5.: fast glass is put into the retort furnace that is warming up to 425 ℃, be incubated after 4 hours, be annealed to about 300 ℃ with 10 ℃/hour speed, and then be annealed to room temperature with 15 ℃/hour speed;
Test result to this glass is as follows:
Get a little sample after the annealing, be ground into fine powdered with agate mortar, carry out differential thermal analysis, the differential thermal curve of low-refraction er-doped fluorine phosphorous glass of the present invention as shown in Figure 1.
The sheet glass that sample after the annealing is processed into 10 * 20 * 3 millimeters also polishes, and measures its specific refractory power, and specific refractory power is as shown in table 1.
Embodiment 2
#:
Form as in the table 12
#Shown in, concrete preparation method comprises the following steps:
1.: the molar percentage of forming by glass (mol%) calculates weight of glass per-cent, takes by weighing raw material then, mixes;
2.: compound is put into corundum crucible, place 1000 ℃ silicon carbon rod electric furnace fusion, according to the length that how much determines melting time of raw material;
3.: behind the glass melting, feed the high pure nitrogen homogenizing, what of raw material aeration time be decided by;
4.: stop logical nitrogen, glass metal is protected clarified at 1000 ℃, what of raw material its time also depend on, then glass metal poured in the mould of preheating;
5.: fast glass is put into the retort furnace that is warming up to 450 ℃, be incubated after 4 hours, be annealed to about 300 ℃ with 10 ℃/hour speed, and then be annealed to room temperature with 15 ℃/hour speed;
Test to this glass is as follows:
Get a little sample after the annealing, be ground into fine powdered, carry out differential thermal analysis with agate mortar;
The sheet glass that sample after the annealing is processed into 10 * 20 * 3 millimeters also polishes, and measures its specific refractory power.
Embodiment 3
#:
Form as in the table 13
#Shown in, concrete preparation method comprises the following steps:
1.: the molar percentage of forming by glass (mol%) calculates weight of glass per-cent, takes by weighing raw material then, mixes;
2.: compound is put into platinum crucible, place 980 ℃ silicon carbon rod electric furnace fusion, according to the length that how much determines melting time of raw material;
3.: behind the glass melting, feed the high pure nitrogen homogenizing, what of raw material aeration time be decided by;
4.: stop logical nitrogen, glass metal is protected clarified at 980 ℃, what of raw material its time also depend on, then glass metal poured in the mould of preheating;
5.: fast glass is put into the retort furnace that is warming up to 440 ℃, be incubated after 4 hours, be annealed to about 300 ℃ with 10 ℃/hour speed, and then be annealed to room temperature with 15 ℃/hour speed;
Test to this glass is as follows:
Get a little sample after the annealing, be ground into fine powdered, carry out differential thermal analysis with agate mortar;
The sheet glass that sample after the annealing is processed into 10 * 20 * 3 millimeters also polishes, and measures its specific refractory power.
Embodiment 4
#:
Form as in the table 14
#Shown in, concrete preparation method comprises the following steps:
1.: the molar percentage of forming by glass (mol%) calculates weight of glass per-cent, takes by weighing raw material then, mixes;
2.: compound is put into platinum crucible, place 1020 ℃ silicon carbon rod electric furnace fusion, according to the length that how much determines melting time of raw material;
3.: behind the glass melting, feed the high pure nitrogen homogenizing, what of raw material aeration time be decided by;
4.: stop logical nitrogen, glass metal is protected clarified at 1020 ℃, what of raw material its time also depend on, then glass metal poured in the mould of preheating;
5.: fast glass is put into the retort furnace that is warming up to 460 ℃, be incubated after 4 hours, be annealed to about 300 ℃ with 10 ℃/hour speed, and then be annealed to room temperature with 15 ℃/hour speed;
Test to this glass is as follows:
Get a little sample after the annealing, be ground into fine powdered, carry out differential thermal analysis with agate mortar;
The sheet glass that sample after the annealing is processed into 10 * 20 * 3 millimeters also polishes, and measures its specific refractory power.
Claims (2)
1, a kind of low-refraction er-doped fluorine phosphorous glass that is used for evanescent wave optical fiber amplifier, feature is that it is composed as follows:
Glass ingredient mol%
Al(PO
3)
3 2.5~5
AlF
3 27~39
MgF
2 6~10
CaF
2 19~26
SrF
2 5~8
BaF
2 7~10
NaF 0,15~20
KF 0~8
ErF
3 3~6。
2, the preparation method of the described low-refraction er-doped of a kind of claim 1 fluorine phosphorous glass is characterised in that to comprise the steps:
1.: the selected molar percentage of pressing the glass composition, calculate corresponding each weight percent of forming, take by weighing each raw material then, mix;
2.: compound is put into corundum crucible, place 950~1020 ℃ silicon carbon rod electric furnace fusion, melting time was controlled at 10~20 minutes;
3.: behind the glass melting, feed the high pure nitrogen homogenizing;
4.: stop logical nitrogen, clarified 10~20 minutes, then glass metal is poured in the mould of preheating;
5.: fast glass is put into the retort furnace that is warming up to glass transformation temperature, be incubated after 4 hours, be cooled to 300 ℃ with 10 ℃/hour speed again, and then be annealed to room temperature with 15 ℃/hour speed.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2005100290541A CN1313404C (en) | 2005-08-24 | 2005-08-24 | Preparation method of low refractivity glass doped with erbium, fluorine and phosphor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2005100290541A CN1313404C (en) | 2005-08-24 | 2005-08-24 | Preparation method of low refractivity glass doped with erbium, fluorine and phosphor |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1765796A true CN1765796A (en) | 2006-05-03 |
CN1313404C CN1313404C (en) | 2007-05-02 |
Family
ID=36741945
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---|---|---|---|
CNB2005100290541A Expired - Fee Related CN1313404C (en) | 2005-08-24 | 2005-08-24 | Preparation method of low refractivity glass doped with erbium, fluorine and phosphor |
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CN (1) | CN1313404C (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101870555A (en) * | 2010-06-11 | 2010-10-27 | 陕西科技大学 | Method for preparing high erbium-doped barium-contained phosphate laser glass |
CN101481212B (en) * | 2009-02-25 | 2011-01-26 | 中国科学院上海光学精密机械研究所 | 2 mu m low phosphorus content fluophosphate laser glass and preparation thereof |
CN102211872A (en) * | 2011-03-23 | 2011-10-12 | 中国科学院上海光学精密机械研究所 | 3 mu m luminous rare earth ion doped fluorophosphates laser glass and preparation method thereof |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03287236A (en) * | 1990-04-03 | 1991-12-17 | Sumitomo Electric Ind Ltd | Optical fiber component |
JPH0629150B2 (en) * | 1990-05-01 | 1994-04-20 | 科学技術庁無機材質研究所長 | Fluoride glass containing rare earth |
JP3145136B2 (en) * | 1991-01-18 | 2001-03-12 | 株式会社住田光学ガラス | Infrared transparent fluoride glass |
JP3287236B2 (en) * | 1996-10-03 | 2002-06-04 | キヤノン株式会社 | Manufacturing method of diffractive optical element |
FR2768143B1 (en) * | 1997-09-05 | 1999-12-03 | Corning Inc | ERBIUM DOPED FLUOROPHOSPHATE GLASS AND OPTICAL AMPLIFIER INCLUDING THIS GLASS |
CN1594160A (en) * | 2004-04-15 | 2005-03-16 | 中国科学院上海光学精密机械研究所 | Low refractive index high concentration Er3 doped fluorine phosphate glass and its preparing method |
-
2005
- 2005-08-24 CN CNB2005100290541A patent/CN1313404C/en not_active Expired - Fee Related
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101481212B (en) * | 2009-02-25 | 2011-01-26 | 中国科学院上海光学精密机械研究所 | 2 mu m low phosphorus content fluophosphate laser glass and preparation thereof |
CN101870555A (en) * | 2010-06-11 | 2010-10-27 | 陕西科技大学 | Method for preparing high erbium-doped barium-contained phosphate laser glass |
CN101870555B (en) * | 2010-06-11 | 2011-12-07 | 陕西科技大学 | Method for preparing high erbium-doped barium-contained phosphate laser glass |
CN102211872A (en) * | 2011-03-23 | 2011-10-12 | 中国科学院上海光学精密机械研究所 | 3 mu m luminous rare earth ion doped fluorophosphates laser glass and preparation method thereof |
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CN1313404C (en) | 2007-05-02 |
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