CN105152175A - Method for utilizing waste heat generated in SiO2 aerogel production - Google Patents

Method for utilizing waste heat generated in SiO2 aerogel production Download PDF

Info

Publication number
CN105152175A
CN105152175A CN201510577933.1A CN201510577933A CN105152175A CN 105152175 A CN105152175 A CN 105152175A CN 201510577933 A CN201510577933 A CN 201510577933A CN 105152175 A CN105152175 A CN 105152175A
Authority
CN
China
Prior art keywords
parts
hours
volume
wadding
wet gel
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.)
Pending
Application number
CN201510577933.1A
Other languages
Chinese (zh)
Inventor
赵东旭
汪树龙
董珂
连佩兵
沈颂良
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.)
ANHUI LONGQUAN SILICON MATERIAL Co Ltd
Original Assignee
ANHUI LONGQUAN SILICON MATERIAL 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 ANHUI LONGQUAN SILICON MATERIAL Co Ltd filed Critical ANHUI LONGQUAN SILICON MATERIAL Co Ltd
Priority to CN201510577933.1A priority Critical patent/CN105152175A/en
Publication of CN105152175A publication Critical patent/CN105152175A/en
Pending legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/10Process efficiency
    • Y02P20/129Energy recovery, e.g. by cogeneration, H2recovery or pressure recovery turbines

Landscapes

  • Silicon Compounds (AREA)

Abstract

The invention provides a method for utilizing waste heat generated in SiO2 aerogel production. The method comprises the steps of adding 50 parts of a dilute sulphuric acid solution into a vessel; dropwise adding a water glass solution under magnetic stirring until the pH value of the solution system is up to 4.5; dropwise adding 2 parts of a drying control chemical additive (DCCA) and 2 parts of absolute ethyl alcohol, and uniformly stirring; after gelling at normal temperature and aging for 2 hours, adding 50 parts of absolute ethyl alcohol to soak for 10 hours; then, adding 50 parts of n-hexane to soak for 11 hours; mashing wet gel, carrying out suction filtration and washing for many times; then, placing the wet gel into a distillation vessel filled with 150 parts of azeotropic distillation medium, uniformly stirring, and carrying out azeotropic distillation by heating until drying by distillation; and next, placing the obtained product into a blast drying oven, and drying at the temperature of 105 DEG C for 2 hours to obtain SiO2 aerogel powder. A sol-gel/azeotropic distillation method is adopted, so that the coagulation process is short, the coagulation effect is good, the uniformity of a gel structure is good, the structure of SiO2 aerogel can be kept not withered and fragmented, and the prepared product is large in pore volume and high in specific surface area.

Description

Residual-heat utilization method in a kind of aerosil production
Technical field
The present invention relates to aerosil production technical field, particularly relate to residual-heat utilization method in the production of a kind of aerosil.
Background technology
Aerosil is a kind of novel light nano-porous materials grown up this year, and it has translucent and that density is ultralight characteristic.Structurally have that voidage is high, density is low, primary particle is little and the feature such as specific surface area is large, be all used widely in all many-sides such as mechanics, acoustics, calorifics, optics and electricity.
The raw material of synthetic silica aerogel mainly adopts expensive tetraethoxy both at home and abroad at present, dry by adopting supercritical technology.Although adopt Supercritical Drying Technology to reduce surface tension; avoid the micropore atrophy of dried aerogel and dry and cracked; then supercritical process requires harsh to drying conditions; equipment is complicated; obvious burden is all caused to cost and safety; can not continuity and large-scale production, thus limit the application of this drying means.Therefore explore and how to maintain aerosil structure the study hotspot that atrophy and other cracked drying process become domestic and international scientific worker does not occur.
Summary of the invention
Residual-heat utilization method in the object of the present invention is to provide a kind of aerosil to produce, to solve the problems of the technologies described above.
Technical problem to be solved by this invention realizes by the following technical solutions:
Residual-heat utilization method in a kind of aerosil production, it is characterized in that: get 50 parts of (volume) dilution heat of sulfuric acid in container, under magnetic stirring, adopt mode first quick and back slow to drip the water glass solution diluted, until the pH of solution system reaches 4.5, then drip 2 parts of (volume) drying control chemical additive DCCA and 2 part of (volume) dehydrated alcohols, after stirring, be placed in gel under normal temperature, after aging 2 hours, obtain SiO 2wet gel;
50 parts of (volume) dehydrated alcohols are added in the wet gel after aging, soak 10 hours, then add 50 parts of (volume) hexanes, soak 11 hours, wet gel is smashed to pieces, suction filtration also washs for several times, then this wet gel is put into the distil container that 150 parts of (volume) component distillation media are housed, stirs, component distillation is carried out in heating, until evaporate to dryness, then remaining sample is placed in air dry oven in 105 DEG C of dryings 2 hours, obtains SiO 2aerogel powder; Described distil container is connected with holding tank by pipeline, and described install pipeline has interlayer, is provided with prolong in interlayer, and heat is taken away and is used for the preheating of other operation by the cooling fluid in prolong.
Described dilute sulphuric acid is that 98% vitriol oil and water are formulated by the volume ratio of 1:30, and described water glass solution is that industrial waterglass and water are formulated by the volume ratio of 1:2.
Gelation process comprises centrifugal solidifying wadding and leaves standstill solidifying two stages of wadding, centrifugal solidifying wadding 1.5 hours, leave standstill solidifying wadding 0.5 hour, centrifugal solidifying wadding to make container rotation centered by its central shaft, makes the fast rapid hardening wadding of container contents, in container rotation process, rotational velocity adopts the mode hocketed of accelerating and slow down, the maximum value of rotational velocity is 120r/min, and the minimum value of rotational velocity is 25r/min, accelerates to be 5s with the time of moderating process.
This solidifying wadding method, solidifying wadding efficiency can be improved and optimize solidifying wadding effect, under the mating reaction accelerated and be rotated in deceleration, impel gel structure homogenizing, prevent stress during drying cause shrink and dry and cracked, the time that traditional natural coagulates wadding is longer, is unfavorable for enhancing productivity, this solidifying wadding method substantially reduces the solidifying wadding time, improves production efficiency.
The invention has the beneficial effects as follows:
The present invention adopts the method for sol-gel/component distillation, and solidifying wadding process is fast, and solidifying wadding is effective, gel structure good evenness, and can maintain aerosil structure and atrophy and cracked does not occur, the product pore volume prepared is large, specific surface area is high.
Embodiment
The technique means realized to make the present invention, creation characteristic, reaching object and effect is easy to understand, below in conjunction with specific embodiment, set forth the present invention further, but following embodiment being only the preferred embodiments of the present invention, and not all.Based on the embodiment in embodiment, those skilled in the art under the prerequisite not making creative work obtain other embodiment, all belong to protection scope of the present invention.
Residual-heat utilization method in a kind of aerosil production, get 50 parts of (volume) dilution heat of sulfuric acid in container, under magnetic stirring, adopt mode first quick and back slow to drip the water glass solution diluted, until the pH of solution system reaches 4.5, then drip 2 parts of (volume) drying control chemical additive DCCA and 2 part of (volume) dehydrated alcohols, after stirring, be placed in gel under normal temperature, after aging 2 hours, obtain SiO 2wet gel;
50 parts of (volume) dehydrated alcohols are added in the wet gel after aging, soak 10 hours, then add 50 parts of (volume) hexanes, soak 11 hours, wet gel is smashed to pieces, suction filtration also washs for several times, then this wet gel is put into the distil container that 150 parts of (volume) component distillation media are housed, stirs, component distillation is carried out in heating, until evaporate to dryness, then remaining sample is placed in air dry oven in 105 DEG C of dryings 2 hours, obtains SiO 2aerogel powder;
Gelation process comprises centrifugal solidifying wadding and leaves standstill solidifying two stages of wadding, centrifugal solidifying wadding 1.5 hours, leave standstill solidifying wadding 0.5 hour, centrifugal solidifying wadding to make container rotation centered by its central shaft, makes the fast rapid hardening wadding of container contents, in container rotation process, rotational velocity adopts the mode hocketed of accelerating and slow down, the maximum value of rotational velocity is 120r/min, and the minimum value of rotational velocity is 25r/min, accelerates to be 5s with the time of moderating process;
Above-mentioned dilute sulphuric acid is that 98% vitriol oil and water are formulated by the volume ratio of 1:30, and above-mentioned water glass solution is that industrial waterglass and water are formulated by the volume ratio of 1:2.
More than show and describe ultimate principle of the present invention, principal character and advantage of the present invention.The technician of the industry should understand; the present invention is not restricted to the described embodiments; what describe in above-described embodiment and specification sheets is only preference of the present invention; be not used for limiting the present invention; without departing from the spirit and scope of the present invention; the present invention also has various changes and modifications, and these changes and improvements all fall in the claimed scope of the invention.Application claims protection domain is defined by appending claims and equivalent thereof.

Claims (3)

1. residual-heat utilization method in an aerosil production, it is characterized in that: get 50 parts of (volume) dilution heat of sulfuric acid in container, under magnetic stirring, adopt mode first quick and back slow to drip the water glass solution diluted, until the pH of solution system reaches 4.5, then drip 2 parts of (volume) drying control chemical additive DCCA and 2 part of (volume) dehydrated alcohols, after stirring, be placed in gel under normal temperature, after aging 2 hours, obtain SiO 2wet gel;
50 parts of (volume) dehydrated alcohols are added in the wet gel after aging, soak 10 hours, then add 50 parts of (volume) hexanes, soak 11 hours, wet gel is smashed to pieces, suction filtration also washs for several times, then this wet gel is put into the distil container that 150 parts of (volume) component distillation media are housed, stirs, component distillation is carried out in heating, until evaporate to dryness, then remaining sample is placed in air dry oven in 105 DEG C of dryings 2 hours, obtains SiO 2aerogel powder; Described distil container is connected with holding tank by pipeline, and described install pipeline has interlayer, is provided with prolong in interlayer, and heat is taken away and is used for the preheating of other operation by the cooling fluid in prolong.
2. residual-heat utilization method in aerosil production according to claim 1, it is characterized in that: described dilute sulphuric acid is that 98% vitriol oil and water are formulated by the volume ratio of 1:30, described water glass solution is that industrial waterglass and water are formulated by the volume ratio of 1:2.
3. residual-heat utilization method in aerosil production according to claim 1, it is characterized in that: gelation process comprises centrifugal solidifying wadding and leaves standstill solidifying two stages of wadding, centrifugal solidifying wadding 1.5 hours, leave standstill solidifying wadding 0.5 hour, centrifugal solidifying wadding to make container rotation centered by its central shaft, make the fast rapid hardening wadding of container contents, in container rotation process, rotational velocity adopts the mode hocketed of accelerating and slow down, the maximum value of rotational velocity is 120r/min, the minimum value of rotational velocity is 25r/min, accelerates to be 5s with the time of moderating process.
CN201510577933.1A 2015-09-10 2015-09-10 Method for utilizing waste heat generated in SiO2 aerogel production Pending CN105152175A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510577933.1A CN105152175A (en) 2015-09-10 2015-09-10 Method for utilizing waste heat generated in SiO2 aerogel production

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510577933.1A CN105152175A (en) 2015-09-10 2015-09-10 Method for utilizing waste heat generated in SiO2 aerogel production

Publications (1)

Publication Number Publication Date
CN105152175A true CN105152175A (en) 2015-12-16

Family

ID=54793304

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510577933.1A Pending CN105152175A (en) 2015-09-10 2015-09-10 Method for utilizing waste heat generated in SiO2 aerogel production

Country Status (1)

Country Link
CN (1) CN105152175A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1605824A (en) * 2003-10-08 2005-04-13 曾维兴 Drying and pulverizing process for preparing powder material with high dispersibility
CN103073008A (en) * 2013-01-31 2013-05-01 中国科学技术大学 Preparation method of silicon dioxide aerogel
CN104760964A (en) * 2015-04-29 2015-07-08 江西安德力高新科技有限公司 Silicon dioxide aerogel preparation method

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1605824A (en) * 2003-10-08 2005-04-13 曾维兴 Drying and pulverizing process for preparing powder material with high dispersibility
CN103073008A (en) * 2013-01-31 2013-05-01 中国科学技术大学 Preparation method of silicon dioxide aerogel
CN104760964A (en) * 2015-04-29 2015-07-08 江西安德力高新科技有限公司 Silicon dioxide aerogel preparation method

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
吴德荣等: "《工业炉及其节能》", 31 March 1990, 机械工业出版社 *
岳瑞丽等: ""Si02气凝胶的溶胶-凝胶/共沸蒸馏法制备及表征"", 《福建师范大学学报》 *

Similar Documents

Publication Publication Date Title
CN105062430B (en) A kind of preparation method of polyethylene glycol/silicon dioxide/expanded graphite composite shape-setting phase-change material
CN102583407B (en) Preparation method of silica aerogel
CN104760964B (en) A kind of preparation method of aerosil
CN105367032A (en) Preparation method of nano heat preservation board
CN105665018A (en) Preparation method and application of composite solid superacid catalyst
CN106554754A (en) The preparation method of polyethylene glycol/nano silicon composite phase-change material
CN104512896B (en) A kind of method utilizing aluminous fly-ash to prepare white carbon and white carbon
CN105174275A (en) Preparation method of silicon dioxide aerogel
CN105197942A (en) Cyclic utilization method for residual heat in silicon dioxide aerogel production
CN105152175A (en) Method for utilizing waste heat generated in SiO2 aerogel production
CN101749926A (en) Method for fast preparing freeze-dried gel nanometer materials
CN105597634A (en) Supercritical drying method for glass wool/silicon-aluminum aerogel composite heat preservation plate
CN107128933A (en) A kind of supercritical drying preparation method of aerosil heat-barrier material
CN115806427A (en) Low-cost SiO 2 Method for producing aerogels
CN111204772A (en) High-purity high-modulus potassium silicate solution and preparation method thereof
CN105605885A (en) Super-critical drying method for fiber needled felt/silicon-aluminum aerogel composite insulation board
CN109437812B (en) Heat-insulating coating and preparation method thereof
CN104774027A (en) Preparation method of tubular ceramic membranes
CN104774024A (en) Preparation process of tubular water treatment membranes
CN103360233A (en) Method for converting neodymium oxide into neodymium acetate crystal
CN105727850A (en) Atmospheric drying method of silicon-aluminum compound aerogel
CN104844244A (en) Process for preparing tubular ceramic film by rotary method
CN105330134A (en) Preparing method for fluorine-high-doped silica glass
CN105439154A (en) Method for preparing low-density silicon dioxide aerogel by two-step method
CN105698489A (en) Normal-pressure drying method of glass wool/aluminum silicon aerogel composite heat preserving board

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20151216