CN1749190A - Method for producing mullite crystal refractory fiber blanket and its product - Google Patents

Method for producing mullite crystal refractory fiber blanket and its product Download PDF

Info

Publication number
CN1749190A
CN1749190A CN 200510012723 CN200510012723A CN1749190A CN 1749190 A CN1749190 A CN 1749190A CN 200510012723 CN200510012723 CN 200510012723 CN 200510012723 A CN200510012723 A CN 200510012723A CN 1749190 A CN1749190 A CN 1749190A
Authority
CN
China
Prior art keywords
making
hour
fiber
blanket
base substrate
Prior art date
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.)
Granted
Application number
CN 200510012723
Other languages
Chinese (zh)
Other versions
CN100396631C (en
Inventor
鹿成洪
鹿成会
鹿明
李京友
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.)
Luyang Energy Saving Materials Co Ltd
Original Assignee
Shandong Luyang Co Ltd
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.)
Filing date
Publication date
Application filed by Shandong Luyang Co Ltd filed Critical Shandong Luyang Co Ltd
Priority to CNB2005100127234A priority Critical patent/CN100396631C/en
Publication of CN1749190A publication Critical patent/CN1749190A/en
Application granted granted Critical
Publication of CN100396631C publication Critical patent/CN100396631C/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Inorganic Fibers (AREA)

Abstract

The present invention is one kind of refractory mullite crystal fiber blanket and its production process. The production process includes the steps of: making colloid, making fiber blank via collecting wool and needle punching, light burning, high temperature treatment, and cutting to form the product. Or, the production process includes the steps of: making colloid, making fiber blank via collecting wool, light burning, needle punching, high temperature treatment, and cutting to form the product. The refractory mullite crystal fiber blanket consists of Al2O3 in 70-72 wt% and SiO2 in 27-29 wt% chemically, and has mullite crystal phase content over 60 %. It has heat conducting coefficient at 1000 deg c of 0.15-0.20 W/m.k and linear change at 1400 deg c for 24 hr less than 1%. Compared with available aluminum silicate fiber blanket, the present invention has 150-400 deg c raised use temperature and thus expanded use range.

Description

A kind of method for making of mullite crystal refractory fiber blanket and the product that makes thereof
Technical field
The invention belongs to the fire-resistant heat insulating material category, be specifically related to a kind of method for making of mullite crystal refractory fiber blanket and the product that makes thereof.
Background technology
The mullite flame-proof fiber is as the new type high temperature lagging material, has high temperature resistant, anticorrosive, premium properties such as thermal conductivity is low, thermostability and good thermal shock, on the hot industry kiln and high temperature service of industrial sectors such as metallurgy, machinery, oil, chemical industry, electronics, pottery, do furnace lining material and lagging material and use, obtained energy-conservation 5%~40% unusual effect; Reach at aspects such as aerospace guided missile and nuclear power and use in composite reinforcing material, support of the catalyst, all received good effect.Therefore be subjected to people's generally attention, some industrially developed country drop into strength unexpectedly mutually, the exploitation multicrystal mullite refractory fabrics.
But because such fibre technology complexity, production difficulty are big, and thin, short, problems such as fragility is big, easy fracture that fiber exists, domestic this series products can only adopt converted top bundle, wet method goods, hydrostatic profile goods in the use of Industrial Stoves at present, and other finely processed products still belong to blank.This has influenced this series products and has used widening of field, and development and exploitation mullite fiber blanket are very necessary.
Summary of the invention
Purpose of the present invention, be to adopt hydrochloric acid soln, aluminium powder, silicon sol, additive preparation to become colloid, and make the fiber base substrate by getting rid of a technology, the fiber base substrate is through after collecting cotton and drying, light-burned processing through certain temperature, pass through acupuncture again, finally pass through the thermal treatment of certain temperature, again a kind of mullite fiber blanket by being cut into.
The present invention reaches its goal of the invention by following technical solution:
Develop a kind of method for making of mullite crystal refractory fiber blanket, it is characterized in that method for making is divided into glue body, system fiber base substrate---collection is cotton, system needle punched blanket, light-burned processing, pyroprocessing---excision forming step, make finished product, division is as follows:
(1) glue body
1. by weight ratio, concentration 8~15% hydrochloric acid solns: aluminium powder=88~90: 10~12,40~80 ℃ reinforced, and 80~100 ℃ were reacted 1~2 hour, and made first liquid;
2. by weight ratio, first liquid: additive: silicic acid sol=10: 1: 3,50~70 ℃ of reactions 1~4 hour, viscosity 1000~4000mp.s when making 50 ℃, solid content is at 30~40% colloid, and is standby;
Described additive is by weight ratio, soft water: polyvinyl alcohol: lactic acid=10: 1: 10 reacts and made in 1~2 hour at 70~90 ℃;
(2) system fiber base substrate---collection is cotton
The above-mentioned colloid of making, by getting rid of a technology, the rotating speed of control wire swaying roller is at 1000~3000 rev/mins, and forming length is the fiber base substrate of 300~500mm;
The above-mentioned fiber base substrate of making is accumulated as certain thickness by 50~140 ℃ temperature drying and through collecting cotton;
(3) system needle punched blanket
Carry out acupuncture by needle loom, carried out drying 0.5~1.5 hour through 100~350 ℃ temperature again, form needle punched blanket;
(4) light-burned processing
The above-mentioned needle punched blanket of making, through 500~800 ℃, light-burned processing 2~2.5 hours;
(5) pyroprocessing---excision forming
After the light-burned processing, under 1100~1350 ℃, handled 1~4 hour again, at last by being cut into the mullite fiber needle punched blanket of desired size.
The method for making of above-mentioned mullite crystal refractory fiber blanket is characterized in that recipe step is as follows:
(1) glue body
1. by weight ratio, concentration 8~15% hydrochloric acid solns: aluminium powder=88~90: 10~12,40~80 ℃ reinforced in batches, and 80~100 ℃ were reacted 1~2 hour, and made first liquid;
2. by weight ratio, first liquid: additive: silicic acid sol=10: 1: 3,50~70 ℃ of reactions 1~4 hour, viscosity 1000~4000mp.s when making 50 ℃, solid content is at 30~40% colloid, and is standby;
Described additive is by weight ratio, soft water: polyvinyl alcohol: lactic acid=10: 1: 10 reacts and made in 1~2 hour at 70~90 ℃;
(2) system fiber base substrate---collection is cotton
The above-mentioned colloid of making, by getting rid of a technology, the rotating speed of control wire swaying roller is at 1000~3000 rev/mins, and forming length is the fiber base substrate of 300~500mm; The above-mentioned fiber base substrate of making carried out drying 0.5~1.5 hour through 100~350 ℃ temperature again by 50~140 ℃ temperature drying and after collecting cotton, being accumulated as certain thickness;
(3) light-burned processing
The above-mentioned fiber base substrate of making, through 500~800 ℃, light-burned processing 2~2.5 hours;
(4) system needle punched blanket
Carry out acupuncture by needle loom, form needle punched blanket;
(5) pyroprocessing---excision forming
After acupuncture is finished, under 1100~1350 ℃, handled 1~4 hour again, at last by being cut into the mullite fiber needle punched blanket of desired size.
The mullite crystal refractory fiber blanket that above-mentioned method for making makes is characterized in that:
(1) its physicals is:
Fibre diameter: 2~6 μ m
φ 〉=0.25mm slag ball content :≤10%
Use temperature: 1500 ℃
Tensile strength: 〉=0.02MPa
The heater wire variation (1400 ℃ * 24h) :≤-1%
Thermal conductivity 0.15~0.20W/mk under 1000 ℃ of the hot-face temperatures
(2) its chemical constitution is: Al 2O 370~72%; SiO 227~29%, surplus is admissible impurity;
(3) its fiber crystalline phase, principal crystalline phase: mullite mullite content 〉=60%.
The method for making of above-mentioned mullite crystal refractory fiber blanket is characterized in that described concentration of hydrochloric acid solution is 9~10%.
This product adopts the X diffractometer to detect, and oikocryst resembles and is mullite, its content 〉=60%.Al in the fiber 2O 3Content is 70~72%, SiO 2Content is 27~30%.Thermal conductivity under 1000 ℃ of this tapetum fibrosum hot-face temperatures is 0.15~0.20W/m.k, heater wire change (1400 ℃ * 24h)<-1%.
Advantage of the present invention: compare with existing aluminum silicate fiber needle punched blanket, advantage of the present invention is to use the temperature height, improves 150~400 ℃ than present alumina silicate fibre blanket use temperature, thereby has enlarged the use range of refractory fibrous material.
Embodiment
Embodiment one:
With concentration is that 8% hydrochloric acid soln and 90: 12 by weight proportion ratio of aluminium powder evenly join in the reaction ax in batch, and is heated to 60~80 ℃, treat hydrochloric acid soln and aluminium powder add finish after, insulation is 2 hours under 80~100 ℃ temperature, makes first liquid.
Adopt this first liquid 100Kg, add additive 10Kg then, add acidic silicasol 30Kg again, be warming up to 70 ℃ and concentrate, concentrate after 1 hour, make the colloid of viscosity 1000mp.s (50 ℃ time),
Additive is by weight ratio, soft water: polyvinyl alcohol: lactic acid=10: 1: 10 reacts and made in 2 hours at 70~80 ℃;
Adopting the solid content in the colloid that above-mentioned technology makes is 30%, is added to colloid in the wire swaying roller then and adjusts wire swaying roller rotating speed to 1000 rev/min to form length be the fiber base substrate of 300-400mm.This fiber base substrate by 50~100 ℃ temperature drying after and be accumulated as certain thickness after, carry out acupuncture by needle loom, and then carry out drying after 1.5 hours through 100~250 ℃ temperature, through 500~600 ℃ light-burned processing 2.5 hours, again through handling under 1100~1350 ℃ the temperature 1~2 hour, at last by being cut into the mullite fiber needle punched blanket of certain size.
This product adopts the X diffractometer to detect, and oikocryst resembles and is mullite, its content 78.5%.Al in the fiber 2O 3Content is 71%, SiO 2Content is 28.5%, and surplus is admissible impurity.Thermal conductivity under 1000 ℃ of this mullite fiber blanket hot-face temperatures is 0.18W/m.k, heater wire change (1400 ℃ * 24h) be-0.9%.
Embodiment two:
With concentration is that 15% hydrochloric acid soln and 88: 10 by weight proportion ratio of aluminium powder evenly join in the reaction ax in batch, and is heated to 40~60 ℃, treat hydrochloric acid soln and aluminium powder add finish after, insulation is 1 hour under 80~100 ℃ temperature, makes first liquid.
Adopt this first liquid 100Kg, add additive 10Kg then, add acidic silicasol 30Kg again, be warming up to 50 ℃ and concentrate, concentrate after 4 hours, make the colloid of viscosity 4000mp.s (50 ℃ time),
Additive is by weight ratio, soft water: polyvinyl alcohol: lactic acid=10: 1: 10 reacts and made in 1 hour at 80~90 ℃;
Adopting the solid content in the colloid that above-mentioned technology makes is 40%, is added to colloid in the wire swaying roller then and adjusts wire swaying roller rotating speed to 3000 rev/min to form length be the fiber base substrate of 400-500mm.This fiber base substrate by 100~140 ℃ temperature drying after and be accumulated as certain thickness after, carry out acupuncture by needle loom, and then carry out drying after 0.5 hour through 250~350 ℃ temperature, through 600~800 ℃ light-burned processing 2 hours, again through handling under 1100~1350 ℃ the temperature 3~4 hours, at last by being cut into the mullite fiber needle punched blanket of certain size.
This product adopts the X diffractometer to detect, and oikocryst resembles and is mullite, its content 78.5%.Al in the fiber 2O 3Content is 72%, SiO 2Content is 27.5%, and surplus is admissible impurity.Thermal conductivity under 1000 ℃ of this mullite fiber blanket hot-face temperatures is 0.15W/m.k, heater wire change (1400 ℃ * 24h) be-0.8%.
Embodiment three:
With concentration is that 8% hydrochloric acid soln and 90: 12 by weight proportion ratio of aluminium powder evenly join in the reaction ax in batch, and is heated to 60~80 ℃, treat hydrochloric acid soln and aluminium powder add finish after, insulation is 2 hours under 80~100 ℃ temperature, makes first liquid.
Adopt this first liquid 100Kg, add additive 10Kg then, add acidic silicasol 30Kg again, be warming up to 70 ℃ and concentrate, concentrate after 1 hour, make the colloid of viscosity 1000mp.s (50 ℃ time),
Additive is by weight ratio, soft water: polyvinyl alcohol: lactic acid=10: 1: 10 reacts and made in 2 hours at 70~80 ℃;
Adopting the solid content in the colloid that above-mentioned technology makes is 30%, is added to colloid in the wire swaying roller then and adjusts wire swaying roller rotating speed to 1000 rev/min to form length be the fiber base substrate of 300-400mm.This fiber base substrate by 50~100 ℃ temperature drying after and be accumulated as certain thickness after, and then carried out drying 1.5 hours through 100~250 ℃ temperature; Through 500~600 ℃ light-burned processing 2.5 hours; Carry out acupuncture by needle loom and form needle punched blanket; Again through handling under 1100~1350 ℃ the temperature 1~2 hour, at last by being cut into the mullite fiber needle punched blanket of certain size.
This product adopts the X diffractometer to detect, and oikocryst resembles and is mullite, its content 78.5%.Al in the fiber 2O 3Content is 71%, SiO 2Content is 28.5%, and surplus is admissible impurity.Thermal conductivity under 1000 ℃ of this mullite fiber blanket hot-face temperatures is 0.18W/m.k, heater wire change (1400 ℃ * 24h) be-0.9%.
Embodiment four:
With concentration is that 15% hydrochloric acid soln and 88: 10 by weight proportion ratio of aluminium powder evenly join in the reaction ax in batch, and is heated to 40~60 ℃, treat hydrochloric acid soln and aluminium powder add finish after, insulation is 1 hour under 80~100 ℃ temperature, makes first liquid.
Adopt this first liquid 100Kg, add additive 10Kg then, add acidic silicasol 30Kg again, be warming up to 50 ℃ and concentrate, concentrate after 4 hours, make the colloid of viscosity 4000mp.s (50 ℃ time),
Additive is by weight ratio, soft water: polyvinyl alcohol: lactic acid=10: 1: 10 reacts and made in 1 hour at 80~90 ℃;
Adopting the solid content in the colloid that above-mentioned technology makes is 40%, is added to colloid in the wire swaying roller then and adjusts wire swaying roller rotating speed to 3000 rev/min to form length be the fiber base substrate of 400-500mm.This fiber base substrate by 50~100 ℃ temperature drying after and be accumulated as certain thickness after, and then carried out drying 0.5 hour through 200~350 ℃ temperature; Through 600~800 ℃ light-burned processing 2 hours; Carry out acupuncture by needle loom and form needle punched blanket; Again through handling under 1100~1350 ℃ the temperature 2~4 hours, at last by being cut into the mullite fiber needle punched blanket of certain size.
This product adopts the X diffractometer to detect, and oikocryst resembles and is mullite, its content 78.5%.Al in the fiber 2O 3Content is 71.2%, SiO 2Content is 28.3%, and surplus is admissible impurity.Thermal conductivity under 1000 ℃ of this mullite fiber blanket hot-face temperatures is 0.15W/m.k, heater wire change (1400 ℃ * 24h) be-0.9%.
Embodiment five
With concentration is that 9% hydrochloric acid soln and 90: 12 by weight proportion ratio of aluminium powder evenly join in the reaction ax in batch, and is heated to 60~80 ℃, treat hydrochloric acid soln and aluminium powder add finish after, insulation is 2 hours under 80~100 ℃ temperature, makes first liquid.
Adopt this first liquid 100Kg, add additive 10Kg then, add acidic silicasol 30Kg again, be warming up to 70 ℃ and concentrate, concentrate after 1 hour, make the colloid of viscosity 1000mp.s (50 ℃ time),
Additive is by weight ratio, soft water: polyvinyl alcohol: lactic acid=10: 1: 10 reacts and made in 2 hours at 70~80 ℃;
Adopting the solid content in the colloid that above-mentioned technology makes is 30%, is added to colloid in the wire swaying roller then and adjusts wire swaying roller rotating speed to 1000 rev/min to form length be the fiber base substrate of 300-400mm.This fiber base substrate by 50~100 ℃ temperature drying after and be accumulated as certain thickness after, carry out acupuncture by needle loom, and then carry out drying after 1.5 hours through 100~250 ℃ temperature, through 500~600 ℃ light-burned processing 2.5 hours, again through handling under 1100~1350 ℃ the temperature 1~2 hour, at last by being cut into the mullite fiber needle punched blanket of certain size.
This product adopts the X diffractometer to detect, and oikocryst resembles and is mullite, its content 78.5%.Al in the fiber 2O 3Content is 71%, SiO 2Content is 28.5%, and surplus is admissible impurity.Thermal conductivity under 1000 ℃ of this mullite fiber blanket hot-face temperatures is 0.18W/m.k, heater wire change (1400 ℃ * 24h) be-0.9%.
Embodiment six
With concentration is that 10% hydrochloric acid soln and 88: 10 by weight proportion ratio of aluminium powder evenly join in the reaction ax in batch, and is heated to 40~60 ℃, treat hydrochloric acid soln and aluminium powder add finish after, insulation is 1 hour under 80~100 ℃ temperature, makes first liquid.
Adopt this first liquid 100Kg, add additive 10Kg then, add acidic silicasol 30Kg again, be warming up to 50 ℃ and concentrate, concentrate after 4 hours, make the colloid of viscosity 4000mp.s (50 ℃ time),
Additive is by weight ratio, soft water: polyvinyl alcohol: lactic acid=10: 1: 10 reacts and made in 1 hour at 80~90 ℃;
Adopting the solid content in the colloid that above-mentioned technology makes is 40%, is added to colloid in the wire swaying roller then and adjusts wire swaying roller rotating speed to 3000 rev/min to form length be the fiber base substrate of 400-500mm.This fiber base substrate by 50~100 ℃ temperature drying after and be accumulated as certain thickness after, and then carried out drying 0.5 hour through 200~350 ℃ temperature; Through 600~800 ℃ light-burned processing 2 hours; Carry out acupuncture by needle loom and form needle punched blanket; Again through handling under 1100~1350 ℃ the temperature 2~4 hours, at last by being cut into the mullite fiber needle punched blanket of certain size.
This product adopts the X diffractometer to detect, and oikocryst resembles and is mullite, its content 78.5%.Al in the fiber 2O 3Content is 70.5%, SiO 2Content is 29%, and surplus is admissible impurity.Thermal conductivity under 1000 ℃ of this mullite fiber blanket hot-face temperatures is 0.15W/m.k, heater wire change (1400 ℃ * 24h) be-0.8%.

Claims (4)

1. excision forming step that the method for making of a mullite crystal refractory fiber blanket is characterized in that method for making is divided into glue body, system fiber base substrate---collection is cotton, system needle punched blanket, light-burned processing, pyroprocessing---makes finished product, and division is as follows:
(1) glue body
1. by weight ratio, concentration 8~15% hydrochloric acid solns: aluminium powder=88~90: 10~12,40~80 ℃ reinforced, and 80~100 ℃ were reacted 1~2 hour, and made first liquid;
2. by weight ratio, first liquid: additive: silicic acid sol=10: 1: 3,50~70 ℃ of reactions 1~4 hour, viscosity 1000~4000mp.s when making 50 ℃, solid content is at 30~40% colloid, and is standby;
Described additive is by weight ratio, soft water: polyvinyl alcohol: lactic acid=10: 1: 10 reacts and made in 1~2 hour at 70~90 ℃;
(2) system fiber base substrate---collection is cotton
The above-mentioned colloid of making, by getting rid of a technology, the rotating speed of control wire swaying roller is at 1000~3000 rev/mins, and forming length is the fiber base substrate of 300~500mm;
The above-mentioned fiber base substrate of making is accumulated as certain thickness by 50~140 ℃ temperature drying and through collecting cotton;
(3) system needle punched blanket
Carry out acupuncture by needle loom, carried out drying 0.5~1.5 hour through 100~350 ℃ temperature again, form needle punched blanket;
(4) light-burned processing
The above-mentioned needle punched blanket of making, through 500~800 ℃, light-burned processing 2~2.5 hours;
(5) pyroprocessing---excision forming
After the light-burned processing, under 1100~1350 ℃, handled 1~4 hour again, at last by being cut into the mullite fiber needle punched blanket of desired size.
2. method for making according to the described mullite crystal refractory fiber blanket of claim 1 is characterized in that recipe step is as follows:
(1) glue body
1. by weight ratio, concentration 8~15% hydrochloric acid solns: aluminium powder=88~90: 10~12,40~80 ℃ reinforced in batches, and 80~100 ℃ were reacted 1~2 hour, and made first liquid;
2. by weight ratio, first liquid: additive: silicic acid sol=10: 1: 3,50~70 ℃ of reactions 1~4 hour, viscosity 1000~4000mp.s when making 50 ℃, solid content is at 30~40% colloid, and is standby;
Described additive is by weight ratio, soft water: polyvinyl alcohol: lactic acid=10: 1: 10 reacts and made in 1~2 hour at 70~90 ℃;
(2) system fiber base substrate---collection is cotton
The above-mentioned colloid of making, by getting rid of a technology, the rotating speed of control wire swaying roller is at 1000~3000 rev/mins, and forming length is the fiber base substrate of 300~500mm; The above-mentioned fiber base substrate of making carried out drying 0.5~1.5 hour through 100~350 ℃ temperature again by 50~140 ℃ temperature drying and after collecting cotton, being accumulated as certain thickness;
(3) light-burned processing
The above-mentioned fiber base substrate of making, through 500~800 ℃, light-burned processing 2~2.5 hours;
(4) system needle punched blanket
Carry out acupuncture by needle loom, form needle punched blanket;
(5) pyroprocessing---excision forming
After acupuncture is finished, under 1100~1350 ℃, handled 1~4 hour again, at last by being cut into the mullite fiber needle punched blanket of desired size.
3. the mullite crystal refractory fiber blanket that makes according to the described method for making of claim 1 is characterized in that:
(1) its physicals is:
Fibre diameter: 2~6 μ m
φ 〉=0.25mm slag ball content :≤10%
Use temperature: 1500 ℃
Tensile strength: 〉=0.02MPa
Heater wire changes, 1400 ℃ * 24h :≤-1%
Thermal conductivity 0.15~0.20W/mk under 1000 ℃ of the hot-face temperatures
(2) its chemical constitution is: Al 2O 370~72%; SiO 227~29%, surplus is admissible impurity;
(3) its fiber crystalline phase, principal crystalline phase: mullite mullite content 〉=60%.
4. according to the method for making of the described mullite crystal refractory fiber blanket of claim 1, it is characterized in that described concentration of hydrochloric acid solution is 9~10%.
CNB2005100127234A 2005-08-05 2005-08-05 Method for producing mullite crystal refractory fiber blanket and its product Active CN100396631C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2005100127234A CN100396631C (en) 2005-08-05 2005-08-05 Method for producing mullite crystal refractory fiber blanket and its product

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2005100127234A CN100396631C (en) 2005-08-05 2005-08-05 Method for producing mullite crystal refractory fiber blanket and its product

Publications (2)

Publication Number Publication Date
CN1749190A true CN1749190A (en) 2006-03-22
CN100396631C CN100396631C (en) 2008-06-25

Family

ID=36604872

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2005100127234A Active CN100396631C (en) 2005-08-05 2005-08-05 Method for producing mullite crystal refractory fiber blanket and its product

Country Status (1)

Country Link
CN (1) CN100396631C (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102182014A (en) * 2011-01-26 2011-09-14 武汉鑫友泰光电科技有限公司 Light quartz fiber felt and preparation method thereof
CN102465358A (en) * 2010-11-19 2012-05-23 山东鲁阳股份有限公司 Preparation method of polycrystalline mullite fiber
CN103225130A (en) * 2012-12-30 2013-07-31 河北联合大学 Method for preparing mullite nanofibers by combination of non-hydrolytic sol-gel technology and electrostatic spinning technology
CN105734833A (en) * 2016-02-04 2016-07-06 河北国美新型建材有限公司 Aluminum silicate thread throwing fiber board and manufacturing method thereof
CN107385670A (en) * 2017-06-30 2017-11-24 长兴泓矿炉料有限公司 A kind of mullite fiber fire smothering blanket for filtering flue gas
CN108251966A (en) * 2018-01-05 2018-07-06 航天特种材料及工艺技术研究所 A kind of mullite fiber precast body and preparation method thereof
CN108385270A (en) * 2018-04-26 2018-08-10 山东鲁阳浩特高技术纤维有限公司 A kind of alumina fibre composite module and preparation method thereof
CN111039690A (en) * 2019-12-26 2020-04-21 山东鲁阳浩特高技术纤维有限公司 Alumina fiber composite module and preparation method thereof
CN111270411A (en) * 2020-04-07 2020-06-12 山东鲁阳浩特高技术纤维有限公司 Preparation method of alumina fiber blanket
CN111455554A (en) * 2020-04-07 2020-07-28 山东鲁阳浩特高技术纤维有限公司 Alumina fiber blanket and preparation method thereof
CN113846424A (en) * 2021-09-26 2021-12-28 航天特种材料及工艺技术研究所 Mullite fiber needled felt and preparation method thereof

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4986638A (en) * 1972-12-25 1974-08-20
CN1260418C (en) * 2002-06-06 2006-06-21 山东鲁阳股份有限公司 Environment protection type ceramic fibre needling blanket
CN1186286C (en) * 2002-06-06 2005-01-26 山东鲁阳股份有限公司 Ceramic fibre thermal-insulating boara and making method thereof

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102465358A (en) * 2010-11-19 2012-05-23 山东鲁阳股份有限公司 Preparation method of polycrystalline mullite fiber
CN102465358B (en) * 2010-11-19 2014-02-19 山东鲁阳股份有限公司 Method for preparing polycrystal mullite fibers
CN102182014A (en) * 2011-01-26 2011-09-14 武汉鑫友泰光电科技有限公司 Light quartz fiber felt and preparation method thereof
CN103225130A (en) * 2012-12-30 2013-07-31 河北联合大学 Method for preparing mullite nanofibers by combination of non-hydrolytic sol-gel technology and electrostatic spinning technology
CN105734833A (en) * 2016-02-04 2016-07-06 河北国美新型建材有限公司 Aluminum silicate thread throwing fiber board and manufacturing method thereof
CN107385670A (en) * 2017-06-30 2017-11-24 长兴泓矿炉料有限公司 A kind of mullite fiber fire smothering blanket for filtering flue gas
CN108251966A (en) * 2018-01-05 2018-07-06 航天特种材料及工艺技术研究所 A kind of mullite fiber precast body and preparation method thereof
CN108251966B (en) * 2018-01-05 2018-12-11 航天特种材料及工艺技术研究所 A kind of mullite fiber precast body and preparation method thereof
CN108385270A (en) * 2018-04-26 2018-08-10 山东鲁阳浩特高技术纤维有限公司 A kind of alumina fibre composite module and preparation method thereof
CN111039690A (en) * 2019-12-26 2020-04-21 山东鲁阳浩特高技术纤维有限公司 Alumina fiber composite module and preparation method thereof
CN111270411A (en) * 2020-04-07 2020-06-12 山东鲁阳浩特高技术纤维有限公司 Preparation method of alumina fiber blanket
CN111455554A (en) * 2020-04-07 2020-07-28 山东鲁阳浩特高技术纤维有限公司 Alumina fiber blanket and preparation method thereof
CN111455554B (en) * 2020-04-07 2021-07-23 山东鲁阳浩特高技术纤维有限公司 Alumina fiber blanket and preparation method thereof
CN111270411B (en) * 2020-04-07 2021-08-06 山东鲁阳浩特高技术纤维有限公司 Preparation method of alumina fiber blanket
CN113846424A (en) * 2021-09-26 2021-12-28 航天特种材料及工艺技术研究所 Mullite fiber needled felt and preparation method thereof

Also Published As

Publication number Publication date
CN100396631C (en) 2008-06-25

Similar Documents

Publication Publication Date Title
CN1749190A (en) Method for producing mullite crystal refractory fiber blanket and its product
CN104086200B (en) Preparation method of mullite fiber
CN101319414B (en) Production method of silicon carbide fiber with high temperature tolerance
CN101565323B (en) Method for preparing microcrystalline glass composite material containing alumina
CN103952796B (en) A kind of preparation method of silicon nitrogen boron continuous ceramic fiber
CN102101769B (en) Nano silicon dioxide microporous heat insulator and preparation method thereof
CN107805064A (en) Preparation method of fiber-reinforced high-temperature-resistant magnesia-alumina spinel aerogel
JP6249956B2 (en) Alumina fiber assembly, its production method and use
CN103193480A (en) Preparation method of high-performance zirconia ceramic fibers
CN100385072C (en) High temp. resisting low thermoconducting flexible ceramics fibre composite paper and its making method
CN103193485A (en) Preparation method for hexagonal boron nitride fiber
WO2013189247A1 (en) Method for preparing bulk c-aln composite aerogel with high strength and high temperature resistance
CN104141180B (en) A kind of preparation method of continuous magnesium aluminum spinel fibre
CN102838106A (en) Method for preparing carbon film by using silicon carbide-enhanced polyimide composite film
CN115160001A (en) Multi-base composite low-heat-conduction refractory brick for garbage incinerator
CN106544757A (en) Get rid of the method that a method prepares polycrystalline alumina fiber
CN116553941B (en) High-temperature-resistant ceramic fiber board and preparation method thereof
Liu et al. Fabrication of continuous SiOC ceramic fibers by polyethylene oxide assisted sol-gel method
CN113235307A (en) Hard heat-preservation viscose-based graphite felt and preparation method thereof
CN106565251A (en) High-strength lightweight refractory fiber and preparation method thereof
CN106517996B (en) The heat-insulating material and preparation method thereof of ultralow thermal conductivity low-shrinkage
CN104831420B (en) A kind of preparation method of boronising silicon nitride fiber
CN1915908A (en) Method for preparing beta-sialon porous material
CN114538942A (en) Thermal shock resistant fiber reinforced aerogel thermal insulation material and preparation method thereof
CN103232226A (en) Preparation method for alumina ceramic with low thermal conductivity and high compressive strength

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C56 Change in the name or address of the patentee
CP01 Change in the name or title of a patent holder

Address after: 256120 Shandong city of Zibo province Yiyuan County Yi River Road No. 11

Patentee after: LUYANG ENERGY-SAVING MATERIALS CO., LTD.

Address before: 256120 Shandong city of Zibo province Yiyuan County Yi River Road No. 11

Patentee before: Luyang Co., Ltd., Shandong