CN101948277B - Method for preparing light porous inorganic gelled material product from gel particles - Google Patents

Method for preparing light porous inorganic gelled material product from gel particles Download PDF

Info

Publication number
CN101948277B
CN101948277B CN2010102748752A CN201010274875A CN101948277B CN 101948277 B CN101948277 B CN 101948277B CN 2010102748752 A CN2010102748752 A CN 2010102748752A CN 201010274875 A CN201010274875 A CN 201010274875A CN 101948277 B CN101948277 B CN 101948277B
Authority
CN
China
Prior art keywords
pore former
light porous
particle
inorganic coagulation
coagulation material
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.)
Expired - Fee Related
Application number
CN2010102748752A
Other languages
Chinese (zh)
Other versions
CN101948277A (en
Inventor
邱树恒
张鲁湘
陆宇兰
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.)
Guangxi University
Original Assignee
Guangxi University
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 Guangxi University filed Critical Guangxi University
Priority to CN2010102748752A priority Critical patent/CN101948277B/en
Publication of CN101948277A publication Critical patent/CN101948277A/en
Application granted granted Critical
Publication of CN101948277B publication Critical patent/CN101948277B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Porous Artificial Stone Or Porous Ceramic Products (AREA)

Abstract

The invention relates to a method for preparing a light porous inorganic gelled material product from gel particles. The method comprises the following steps of: preparing pore former particles of which the particle sizes are between 0.5 and 5 millimeters from a natural linear polysaccharide polymer and a gelled cross-linking agent; and doping the pore former particles separately or together with expanded perlite particles and polystyrene foam particles into an inorganic gel material in a compounding mode according to different proportions so as to obtain the light porous material product. The volume density, intensity, pore size and density distribution of the material can be conveniently adjusted by altering the particle size and mixing amount of the pore former particles. The heat conductivity coefficient of the prepared light porous material is only between 0.12 and 0.17 w/m.k and high heat preserving performance and high heat insulating performance are achieved. The material can be used for molding and manufacturing materials having requirements on light weight, heat preservation, heat insulation, sound insulation, energy conservation and the like. The preparation method has the advantages of simpleness, safety, low energy consumption and easy control and adjustment.

Description

Prepare the method for light porous inorganic coagulation material goods with gel particle
Technical field
The present invention relates to prepare the method for light porous inorganic coagulation material goods, be used to make porous light-weight material with heat insulating and sound-proofing properties with gel particle.
Background technology
Current, China's rapid economic development, under the prerequisite of the strategy of sustainable development, all trades and professions all propose the requirement of saving energy and reduce the cost.Light porous material is as a kind of novel material of construction and heat preserving and insulating material, has in light weight, heat insulating, sound insulation, anti-aging, good characteristic such as fire performance is good, meets green, environmental protection, the energy-conservation requirement stressed day by day in recent years.Present most of lightweight and porous material also adopt frothing aid when moulding, to foam except adopting light-weight aggregate.Because sample is higher to the conditional request of foaming pore-forming at the maintenance initial stage; In foaming process, can produce the merging of part bubble, come-up and the unequal bad phenomenon of void distribution; Cause formed void shape and not of uniform size, and sphericity is relatively poor, bearing capacity is lower; Add the shape size of hole and distribute wayward, can not the fine needs that satisfy various light porous materials.The air-entrained concrete building block of present architectural use though can strengthen the heat insulating effect of buildings, all need pass through the HTHP boiling in process of production, consume mass energy.
Summary of the invention
The purpose of this invention is to provide a kind of make spherical hole size in the inorganic coagulation material goods close, be evenly distributed, hole size and density can be regulated, process for preparation need not to heat prepares the method for light porous inorganic coagulation material goods with gel particle.
The present invention solves the problems of the technologies described above with following scheme:
The process step that single pore former particle is mixed preparation light porous material in the inorganic coagulation material is:
1. be 0.7%~1.3% sodium alginate soln with concentration, use spraying equipment to be injected in the calcium chloride solution that concentration is 0.5~1.5mol/L, reacted 5~20 minutes, the gel particle of the high-moisture that makes gets the pore former particle with flushing with clean water;
2. be 30%~90% to be incorporated in inorganic coagulation material cement or gypsum or the ground polymers material the pore former particle according to the volume percent of piling up; Add the water stirring and process uniform slip, go into mould, the demoulding after 24 hours; Natural curing makes the inorganic coagulation material goods of light porous property.
The process step of pore former particle and expanded perlite granule or polystyrene foam particles being mixed again the preparation light porous material is:
1. be 0.7%~1.3% sodium alginate soln with concentration, use spraying equipment to be injected in the calcium chloride solution that concentration is 0.5~1.5mol/L, reacted 5~20 minutes, the gel particle of the high-moisture that makes gets the pore former particle with flushing with clean water;
2. carry out composite according to 1: 3~3: 1 volume ratio pore former particle and expanded perlite granule or polystyrene foam particles; Composite gathering materials mixed in the inorganic coagulation material by 30%~90% volume percent; Add the water stirring and process uniform slip, go into mould, the demoulding after 24 hours; Through natural curing, make inorganic coagulation material goods with light porous property.
The pore former particle can be regulated with pressure through changing the shower nozzle aperture, and the control particle diameter and carries out size classification with screen cloth and puts into clear water afterwards and preserve between 0.5~5mm.
The beneficial effect of the inventive method is:
1, can regulate hole size and hole density in the goods as required within the specific limits, density through the control hole and the ratio that light-weight aggregate is mixed are again controlled the volume density and the intensity of light porous material;
2, the hole majority that forms in the sample is a spherical pore, and spherical hole size is close, be evenly distributed, and the light material load performance with spherical pore is better relatively;
3, process for preparation need not to heat, and maintenance processes is consumed energy not, can mix mutually with other light-weight aggregates;
The thermal conductivity of the light porous material of 4, processing only between 0.12~0.17w/m.k, has good thermal and insulating performance.The moulding and the making of the material that can be used for lightweight, insulation, heat insulation, sound insulation, energy-conservation etc. required;
5. the method for preparing pore former and be mixed with light porous material with this pore former and gelling material is all very simple, convenient, safely, be easy to control and regulate; Energy consumption is low, and it is different also can to make performance, the multiple light porous material that purposes is different.
Description of drawings
Fig. 1 is a test block tangent plane photo.
Fig. 2 is the local photo that amplifies 10 times of test block tangent plane.
Embodiment
Method of the present invention mainly is to have utilized because the dehydration drying of gel particle has formed the principle of hole in hardened inorganic coagulation material inside; Guaranteed that light porous material goods thermal conductivity is low; The preparation power consumption is few; The inner hole of the light porous material that makes is many and spare, and hole size, controllable density system.
(1) pore former particulate preparation
1. sodium-alginate is a kind of natural line style polysaccharide polymer, have well water-soluble, as the gelation mother liquor.Compound concentration is 0.7%~1.3% sodium alginate aqueous solution by mass percentage: 20~80 ℃ of following mechanical stirring it is dissolved in the water sodium-alginate; (wherein in the time of 60 ℃, stir, the dissolved net effect is best;) form the sodium alginate aqueous solution of transparent and homogeneous, it is for use to be cooled to room temperature.
2. adopt calcium chloride as the gelation linking agent.The calcium chloride solution of preparation 0.5~1.5mol/L is preserved for use.
3. the sodium alginate soln that obtains step 1; Be injected in the calcium chloride solution that step 2 obtains with spraying equipment; Can form the high-moisture gel particle, these gel particles reacted in calcium chloride solution 5~20 minutes, took out and use flushing with clean water then; Make the pore former particle, after screen cloth carries out size grading, put into clear water and preserve for use.
The pore former particle grain size can be regulated through adopting different shower nozzle aperture and pressure, and the control particle diameter is between 0.5~5mm.Gained pore former particulate water cut >=92%.
In preparation pore former particulate process, as long as the concentration of linking agent calcium chloride solution is remained on certain level, the preparation of pore former particulate just can be carried out continuously.
(2) preparation of light porous material
1, the pore former particle that makes is mixed separately prepares light porous material in the inorganic coagulation material.Can be 30%~90% to be incorporated in inorganic coagulation material such as cement or the gypsum etc. according to the volume percent of piling up with the pore former particle during preparation, add water and stir and process uniform slip, go into mould, the demoulding after 24 hours, natural curing.In maintenance processes, owing to the dehydration gradually of pore former particle, contraction, the further aquation that can be cement on the one hand provides moisture content, produces hole owing to shrinking on the other hand, thereby makes the inorganic materials goods with light porous property.
2, carry out pore former particle and light-weight aggregate such as expanded perlite granule and/or polystyrene foam particles composite according to 1: 3~3: 1 volume ratio; Composite gathering materials mixed in inorganic coagulation material cement or the gypsum etc. by 30%~90% volume percent; Add the water stirring and process distributed slurry, go into mould, the demoulding after 24 hours; After natural curing, can make light porous inorganic materials goods.
Embodiment 1:
Gather materials (particle diameter is between 2~3mm) with the conduct of pore former particle, and join in the grout according to different volumes per-cent, after stirring, injection molding, maintenance, process light porous concrete test block, concrete proportioning and detected result are as shown in the table:
Table 1 gathers materials and is pore former particulate concrete formulation and performance
1. the W/C in the table is a wc.
2. the volume that gathers materials is represented is pore former particle or the composite shared percent by volume when in mould, piling up of gathering materials.
7 days ultimate compression strength of prepared light porous concrete test block is between 0.61-6.37Mpa, and 28 days ultimate compression strength is between 0.82-6.62Mpa, and dry state density is at 472.7-881.7kg/m 3Between.
Embodiment 2:
Gather materials with pore former particle and the composite conduct of expanded perlite granule, and join in the grout according to different ratios and volume percent.After stirring, injection molding, maintenance, prepare light porous concrete test block.The performance of concrete proportioning and made light porous concrete test block like following table 2 with shown in the table 3:
Table 2 gathers materials and is pore former particle (A) and the composite concrete proportioning table of expanded perlite granule (B)
Figure BSA00000260544200042
Table 3 gathers materials and is pore former particle (A) and the composite concrete performance of expanded perlite granule (B)
Figure BSA00000260544200051
7 days ultimate compression strength of prepared light porous concrete test block is between 2.33-5.71Mpa, and 28 days ultimate compression strength is between 0.89-7.03Mpa, and dry state density is at 534.5-896.73kg/m 3Between.
Embodiment 3:
Gather materials with pore former particle and the composite conduct of polystyrene foam particles, and join in the middle of the cement slurry according to different ratios and volume percent.After stirring, injection molding, maintenance, process light porous concrete test block.The performance of concrete proportioning and made light porous concrete test block like following table 4 with shown in the table 5:
Table 4 gathers materials and is pore former particle (A) and the composite proportioning table of polystyrene foam particles (C)
Table 5 gathers materials and is pore former particle (A) and the composite concrete performance of polystyrene foam particles (C)
Figure BSA00000260544200061
7 days ultimate compression strength of prepared light porous concrete test block is between 3.58-7.08Mpa, and 28 days ultimate compression strength is between 3.95-8.78Mpa, and dry state density is at 634.4-858.4kg/m 3Between.
Embodiment 4:
Separately pore former particle (volume ratio is 90%) is joined in the cement slurry as gathering materials, after stirring, injection molding, maintenance, process light porous concrete test block.Fig. 1 and Fig. 2 are respectively the tangent plane photo and the local photo that amplifies 10 times of test block tangent plane of present embodiment gained test block; Can know from photo and to find out: form spherical hole after the pore former particle dehydration drying; The aperture overwhelming majority is between 1~2mm, and the hole is evenly distributed on tangent plane, the regular shape in hole; And internal surface is smooth, and the light porous concrete test block that this method is processed has bearing capacity preferably.

Claims (3)

1. prepare the method for light porous inorganic coagulation material goods with gel particle for one kind, it is characterized in that the process step that single pore former particle is mixed preparation light porous material in the inorganic coagulation material is:
With mass percent concentration is 0.7%~1.3% sodium alginate soln, uses spraying equipment to be injected in the calcium chloride solution that concentration is 0.5~1.5mol/L, reacts 5~20 minutes, and the gel particle of the high-moisture that makes gets the pore former particle with flushing with clean water;
Is 30%~90% to be incorporated in the inorganic coagulation material the pore former particle according to the volume percent of piling up; Said inorganic coagulation material is cement or gypsum or ground polymers material; Add the water stirring and process uniform slip, go into mould, the demoulding after 24 hours; Natural curing makes the inorganic coagulation material goods of light porous property.
2. prepare the method for light porous inorganic coagulation material goods with gel particle for one kind, it is characterized in that the process step of pore former particle and expanded perlite granule or polystyrene foam particles being mixed again the preparation light porous material is:
With mass percent concentration is 0.7%~1.3% sodium alginate soln, uses spraying equipment to be injected in the calcium chloride solution that concentration is 0.5~1.5mol/L, reacts 5~20 minutes, and the gel particle of the high-moisture that makes gets the pore former particle with flushing with clean water;
Carry out composite according to 1: 3~3: 1 volume ratio pore former particle and expanded perlite granule or polystyrene foam particles; Composite gathering materials mixed in the inorganic coagulation material by 30%~90% volume percent; Add the water stirring and process uniform slip, go into mould, the demoulding after 24 hours; Through natural curing, make inorganic coagulation material goods with light porous property.
According to claim 1 or claim 2 prepare the method for light porous inorganic coagulation material goods with gel particle; It is characterized in that the pore former particle can regulate through changing shower nozzle aperture and pressure; The control particle diameter and carries out putting into clear water after the size classification with screen cloth and preserves between 0.5~5mm.
CN2010102748752A 2010-09-08 2010-09-08 Method for preparing light porous inorganic gelled material product from gel particles Expired - Fee Related CN101948277B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2010102748752A CN101948277B (en) 2010-09-08 2010-09-08 Method for preparing light porous inorganic gelled material product from gel particles

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2010102748752A CN101948277B (en) 2010-09-08 2010-09-08 Method for preparing light porous inorganic gelled material product from gel particles

Publications (2)

Publication Number Publication Date
CN101948277A CN101948277A (en) 2011-01-19
CN101948277B true CN101948277B (en) 2012-11-14

Family

ID=43451927

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2010102748752A Expired - Fee Related CN101948277B (en) 2010-09-08 2010-09-08 Method for preparing light porous inorganic gelled material product from gel particles

Country Status (1)

Country Link
CN (1) CN101948277B (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107573092A (en) * 2017-10-24 2018-01-12 西南科技大学 A kind of porous material and preparation method thereof
CN108546031A (en) * 2018-04-24 2018-09-18 常州五荣化工有限公司 A kind of preparation method of foam concrete
CN111848104A (en) * 2020-07-29 2020-10-30 湖州南浔兴云建材有限公司 Preparation method of environment-friendly safe low-cost sound-insulation and heat-insulation building block
CN115030133B (en) * 2022-06-28 2023-09-22 广州市北二环交通科技有限公司 Soft soil foundation treatment method capable of reducing water damage of soft soil foundation

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6136867A (en) * 1995-04-03 2000-10-24 Rhone-Poulenc Chimie Aqueous suspension of silica and of aluminium sulphate or of alum, processes for the preparation and uses of the said suspension
CN1439618A (en) * 2003-03-21 2003-09-03 中国科学院上海硅酸盐研究所 Preparation of porous calsium silicate/beta-tricalsium phosphate composite bio-ceramic materials
CN1557778A (en) * 2004-02-03 2004-12-29 同济大学 Process for preparation of nano multiporous silicon dioxide aerogel block
CN1749214A (en) * 2005-08-01 2006-03-22 中国人民解放军国防科学技术大学 Aerogel heat insulation composite material and its preparing method
CN1861250A (en) * 2005-05-12 2006-11-15 同济大学 Composite absorption filtering material contg. porous aerogel, and its prepn. method
CN101579643A (en) * 2009-06-11 2009-11-18 湖州师范学院 Sol-gel in situ preparation method of titanium dioxide nano powder coated with alginate
CN101628804A (en) * 2008-07-18 2010-01-20 山东鲁阳股份有限公司 Aerogel heat insulation composite material and preparation method thereof

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU866129A1 (en) * 1978-07-06 1981-09-25 Северо-Западное Территориальное Геологическое Управление Method of preparing plugging composition
JP2003253280A (en) * 2002-02-28 2003-09-10 Yamanaka Co Ltd Solid fuel

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6136867A (en) * 1995-04-03 2000-10-24 Rhone-Poulenc Chimie Aqueous suspension of silica and of aluminium sulphate or of alum, processes for the preparation and uses of the said suspension
CN1439618A (en) * 2003-03-21 2003-09-03 中国科学院上海硅酸盐研究所 Preparation of porous calsium silicate/beta-tricalsium phosphate composite bio-ceramic materials
CN1557778A (en) * 2004-02-03 2004-12-29 同济大学 Process for preparation of nano multiporous silicon dioxide aerogel block
CN1861250A (en) * 2005-05-12 2006-11-15 同济大学 Composite absorption filtering material contg. porous aerogel, and its prepn. method
CN1749214A (en) * 2005-08-01 2006-03-22 中国人民解放军国防科学技术大学 Aerogel heat insulation composite material and its preparing method
CN101628804A (en) * 2008-07-18 2010-01-20 山东鲁阳股份有限公司 Aerogel heat insulation composite material and preparation method thereof
CN101579643A (en) * 2009-06-11 2009-11-18 湖州师范学院 Sol-gel in situ preparation method of titanium dioxide nano powder coated with alginate

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
JP昭55-36589A 1980.03.14
JP特开2003-253280A 2003.09.10

Also Published As

Publication number Publication date
CN101948277A (en) 2011-01-19

Similar Documents

Publication Publication Date Title
CN103011896B (en) Foam concrete
CN103951350B (en) A kind of structural thermal insulation lightweight aggregate concrete
CN103030357B (en) Heat-insulation slurry composition and applications thereof
CN104140230B (en) A kind of gas concrete dry-mixed plastering mortar and preparation method thereof
CN103664114B (en) Self-heat-insulating fly ash autoclaved aerated concrete block and preparation method thereof
CN102010166B (en) Method for preparing micro expanded inorganic heat insulation mortar
CN105130354A (en) Plastering gypsum and preparation method thereof
CN105523740B (en) A kind of heat-insulating light concrete material and preparation method thereof
CN102936127B (en) Light hollow ceramsite and production method thereof
CN104119099B (en) A kind of regenerated foam concrete and preparation method thereof
CN101948277B (en) Method for preparing light porous inorganic gelled material product from gel particles
CN106187311A (en) Polystyrene cement composite heat preserving material and preparation method thereof
CN103408272A (en) Design method of ceramsite foam concrete
CN104355656A (en) Foam concrete and preparation method thereof
CN108439887A (en) A kind of foam concrete block and preparation method thereof
CN103601454A (en) Preparation method of light-weight thermal mortar
CN102775098A (en) Fireproof heat-insulating material as well as preparation method and application thereof
CN110372290A (en) A kind of large dosage volcanic ash foam concrete material and preparation method thereof
CN105130327B (en) A kind of modification is got angry additive and its large dosage tailing wet slag lightweight concrete
CN103011879B (en) Inorganic foaming cement heat insulation board and fabrication method thereof
CN108002792A (en) A kind of machine spray type inorganic heat preservation anticracking grout and its construction method
CN108658537A (en) A kind of maize straw and polymer-modified cement composite architectural materials
CN103693915B (en) A kind of polystyrene foam particles mortar
CN105016648A (en) Concrete additive and light composite block applying same
CN102557559A (en) Inorganic building external wall heat-insulation material and producing process

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
CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20121114

Termination date: 20210908