CN108395275B - 一种轻质多孔大理石复合砖的制备方法 - Google Patents

一种轻质多孔大理石复合砖的制备方法 Download PDF

Info

Publication number
CN108395275B
CN108395275B CN201810300698.7A CN201810300698A CN108395275B CN 108395275 B CN108395275 B CN 108395275B CN 201810300698 A CN201810300698 A CN 201810300698A CN 108395275 B CN108395275 B CN 108395275B
Authority
CN
China
Prior art keywords
marble
parts
weight
mixing
hours
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.)
Active
Application number
CN201810300698.7A
Other languages
English (en)
Other versions
CN108395275A (zh
Inventor
刘凡领
许玉
张烨
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.)
Zaozhuang Xinwoyan Building Materials Co.,Ltd.
Original Assignee
Taizhou Fengfei Machinery Equipment 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 Taizhou Fengfei Machinery Equipment Co Ltd filed Critical Taizhou Fengfei Machinery Equipment Co Ltd
Priority to CN201810300698.7A priority Critical patent/CN108395275B/zh
Publication of CN108395275A publication Critical patent/CN108395275A/zh
Application granted granted Critical
Publication of CN108395275B publication Critical patent/CN108395275B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B38/00Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
    • C04B38/06Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof by burning-out added substances by burning natural expanding materials or by sublimating or melting out added substances
    • C04B38/063Preparing or treating the raw materials individually or as batches
    • C04B38/0635Compounding ingredients
    • C04B38/0645Burnable, meltable, sublimable materials
    • C04B38/067Macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/03Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on magnesium oxide, calcium oxide or oxide mixtures derived from dolomite
    • C04B35/057Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on magnesium oxide, calcium oxide or oxide mixtures derived from dolomite based on calcium oxide
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/626Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
    • C04B35/63Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
    • C04B35/632Organic additives
    • C04B35/634Polymers
    • C04B35/63404Polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/626Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
    • C04B35/63Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
    • C04B35/632Organic additives
    • C04B35/634Polymers
    • C04B35/63404Polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C04B35/63444Nitrogen-containing polymers, e.g. polyacrylamides, polyacrylonitriles, polyvinylpyrrolidone [PVP], polyethylenimine [PEI]
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/71Ceramic products containing macroscopic reinforcing agents
    • C04B35/78Ceramic products containing macroscopic reinforcing agents containing non-metallic materials
    • C04B35/80Fibres, filaments, whiskers, platelets, or the like
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B38/00Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
    • C04B38/0022Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof obtained by a chemical conversion or reaction other than those relating to the setting or hardening of cement-like material or to the formation of a sol or a gel, e.g. by carbonising or pyrolysing preformed cellular materials based on polymers, organo-metallic or organo-silicon precursors
    • C04B38/0025Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof obtained by a chemical conversion or reaction other than those relating to the setting or hardening of cement-like material or to the formation of a sol or a gel, e.g. by carbonising or pyrolysing preformed cellular materials based on polymers, organo-metallic or organo-silicon precursors starting from inorganic materials only, e.g. metal foam; Lanxide type products
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/34Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3409Boron oxide, borates, boric acids, or oxide forming salts thereof, e.g. borax
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/40Metallic constituents or additives not added as binding phase
    • C04B2235/405Iron group metals
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/44Metal salt constituents or additives chosen for the nature of the anions, e.g. hydrides or acetylacetonate
    • C04B2235/444Halide containing anions, e.g. bromide, iodate, chlorite
    • C04B2235/445Fluoride containing anions, e.g. fluosilicate

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Compositions Of Oxide Ceramics (AREA)

Abstract

本发明公开了一种轻质多孔大理石复合砖的制备方法,属于建筑材料技术领域。本发明首先将大理石粉碎过筛后,分散于无水乙醇中,再加入聚乙烯吡咯烷酮,制得大理石分散液,随后将正硅酸乙酯溶液滴加至大理石分散液中,并调节pH至碱性,恒温搅拌反应后,再加入硼酸、纳米铁粉和氟化钠,制得改性大理石分散液,接着将丙烯酰胺、N,N’‑亚甲基双丙烯酰胺、引发剂和改性大理石分散液加热搅拌反应,并过滤,得滤饼湿料,再将滤饼湿料注模后压制成型,随后干燥、脱模并烧制成型,即得轻质多孔大理石复合砖。本发明所得轻质多孔大理石复合砖具有优异的力学性能。

Description

一种轻质多孔大理石复合砖的制备方法
技术领域
本发明公开了一种轻质多孔大理石复合砖的制备方法,属于建筑材料技术领域。
背景技术
现今人们生活水准的不断提升,使得日常生活中的衣、食、住、行和娱乐,等各种方面的品质要求越来越高,实用性上更是越来越好,而在住得方面,除了要求住得舒服,一般在装修的时候还会考虑到建筑材料环保问题。
现在市场上的大理石一般是直接从矿山开采过来,经过简单的抛光处理,直接卖到市面上了,大理石材料需要经过数百年的进化才能形成,材料严重浪费,并且大理石比较重,会增加建筑体的重量,影响建筑高度和防震效果。
大理石砖是指由大理石做成的瓷砖,用作建筑装修,安装后兼具装饰性和功能性,砖的质量及其天然的美丽外观有助于创造出一系列不同类型,不同的颜色,图案及纹理的大理石砖组合;大理石砖具有高耐磨性、高光洁度的特点。但是目前传统的大理石砖还存在力学性能不佳的问题,因此还需对其进行研究。
发明内容
本发明主要解决的技术问题是:针对传统大理石砖力学性能不佳的问题,提供了一种轻质多孔大理石复合砖的制备方法。
为了解决上述技术问题,本发明所采用的技术方案是:
(1)将大理石粉碎,过筛,得细化大理石粉,将细化大理石粉和无水乙醇按质量比为1:8~1:10混合后,超声分散,再加入无水乙醇质量10~20%的聚乙烯吡咯烷酮,恒温搅拌混合24~36h,得大理石分散液;
(2)按重量份数计,依次取20~30份正硅酸乙酯溶液,6~8份硼酸,0.6~0.8份纳米铁粉,4~6份氟化钠,80~100份大理石分散液,将正硅酸乙酯溶液滴加至大理石分散液中,并调节pH至9.6~9.8,恒温搅拌反应24~36h后,再加入硼酸、纳米铁粉和氟化钠,继续搅拌混合2~4h,得改性大理石分散液;
(3)按重量份数计,依次取20~30份丙烯酰胺,6~8份N,N’-亚甲基双丙烯酰胺,2~4份引发剂,60~80份改性大理石分散液,混合后,加热搅拌反应8~12h,再经过滤,得滤饼湿料;
(4)将所得滤饼湿料注入模具中,压制成型后,干燥,脱模,得砖坯,并将所得砖坯于氩气保护状态下,程序升温至1400~1500℃,保温反应2~4h后,于空气气氛中,于温度为1000~1100℃烧结3~5h,冷却,出料,得轻质多孔大理石复合砖。
步骤(1)所述过筛为过500~800目的圆孔筛。
步骤(2)所述正硅酸乙酯溶液是由正硅酸乙酯和无水乙醇按体积比为1:5~1:8混合而成。
步骤(3)所述引发剂为过硫酸铵或过硫酸钾中的任意一种。
本发明的有益效果是:
(1)本发明首先采用机械粉碎对大理石进行细化处理,细化后的大理石表面活性较高,容易发生团聚,且形状不规则,表面缺陷较多,甚至有微裂纹存在,本发明首先采用超声处理打开细化大理石粉末之间的软团聚,然后再加入聚乙烯吡咯烷酮,利用其为表面修饰剂,使其吸附在细化大理石表面,从而使细化大理石可良好稳定分散于无水乙醇体系中,在整个制备过程中,皆可有效稳定分散,从而保障了产品内部的孔隙率,达到轻质效果,另外,经聚乙烯吡咯烷酮修饰后的大理石表面吸附性能得以提升,从而可有效吸附正硅酸乙酯水解产生的二氧化硅,从而弥补细化大理石表面的缺陷结构,使产品烧制之后的强度得到有效提升;
(2)本发明通过采用丙烯酰胺为单体,在交联剂和引发剂作用下发生聚合,形成高分子网络凝胶体,并将稳定分散的细化大理石固定在凝胶体中,在后续高温过程中,高分子网络凝胶体逐渐发生炭化,形成的炭化有机质在纳米铁粉和氟化钠催化条件下,与二氧化硅发生反应,从而形成碳化硅增强体,而残留的炭化有机质在后续空气氛围中得以去除,并在体系内部留下丰富的孔道,使产品力学性能得到提升的同时,容重有效降低,而纳米铁粉在空气氛围中,在高温条件下氧化转变为氧化铁,氧化铁可作为助烧剂,提高产品的烧结效率,使产品性能进一步提升。
具体实施方式
将大理石倒入粉碎机中,粉碎后过500~800目的圆孔筛,得细化大理石粉,再将细化大理石粉和无水乙醇按质量比为1:8~1:10混合后,转入超声分散仪,于超声频率为45~55kHz条件下,超声分散45~60min,待分散结束,再加入无水乙醇质量10~20%的聚乙烯吡咯烷酮,并于温度为45~55℃,转速为300~500r/min条件下,恒温搅拌混合24~36h,出料,得大理石分散液;按重量份数计,依次取20~30份正硅酸乙酯溶液,6~8份硼酸,0.6~0.8份纳米铁粉,4~6份氟化钠,80~100份大理石分散液,先将大理石分散液加入四口烧瓶中,并将四口烧瓶移入数显测速恒温磁力搅拌器,设定搅拌转速为400~600r/min,温度为50~60℃,再于恒温搅拌状态下,通过滴液漏斗向四口烧瓶中滴加正硅酸乙酯溶液,控制滴加速率为4~8mL/min,待正硅酸乙酯溶液滴加完毕,用氨水调节四口烧瓶中物料pH至9.6~9.8,继续恒温搅拌反应24~36h后,再向四口烧瓶中加入硼酸,纳米铁粉和氟化钠,继续搅拌混合2~4h后,出料,得改性大理石分散液;按重量份数计,依次取20~30份丙烯酰胺,6~8份N,N’-亚甲基双丙烯酰胺,2~4份引发剂,60~80份改性大理石分散液,混合倒入三口烧瓶中,并将三口烧瓶移入数显测速恒温磁力搅拌器,于温度为80~85℃,转速为400~500r/min条件下,恒温搅拌反应8~12h,过滤,得滤饼湿料;再将所得滤饼湿料注入模具中,于压力为8~10MPa条件下压制成型后,将模具移入温度为105~110℃的烘箱中,干燥至恒重,脱模,得砖坯,并将所得砖坯移入烧结炉中,并以600~800mL/min速率向炉内通入氩气保护,于氩气保护状态下,以4~8℃/min速率程序升温至1400~1500℃,保温反应2~4h后,停止通入氩气,并以4~8℃/min速率降温至1000~1100℃,于空气气氛中,保温烧结3~5h,随炉冷却至室温,出料,即得轻质多孔大理石复合砖。所述正硅酸乙酯溶液是由正硅酸乙酯和无水乙醇按体积比为1:5~1:8混合而成。所述引发剂为过硫酸铵或过硫酸钾中的任意一种。
实例1
将大理石倒入粉碎机中,粉碎后过800目的圆孔筛,得细化大理石粉,再将细化大理石粉和无水乙醇按质量比为1:10混合后,转入超声分散仪,于超声频率为55kHz条件下,超声分散60min,待分散结束,再加入无水乙醇质量20%的聚乙烯吡咯烷酮,并于温度为55℃,转速为500r/min条件下,恒温搅拌混合36h,出料,得大理石分散液;按重量份数计,依次取30份正硅酸乙酯溶液,8份硼酸,0.8份纳米铁粉,6份氟化钠,100份大理石分散液,先将大理石分散液加入四口烧瓶中,并将四口烧瓶移入数显测速恒温磁力搅拌器,设定搅拌转速为600r/min,温度为60℃,再于恒温搅拌状态下,通过滴液漏斗向四口烧瓶中滴加正硅酸乙酯溶液,控制滴加速率为8mL/min,待正硅酸乙酯溶液滴加完毕,用氨水调节四口烧瓶中物料pH至9.8,继续恒温搅拌反应36h后,再向四口烧瓶中加入硼酸,纳米铁粉和氟化钠,继续搅拌混合4h后,出料,得改性大理石分散液;按重量份数计,依次取30份丙烯酰胺,8份N,N’-亚甲基双丙烯酰胺,4份引发剂,80份改性大理石分散液,混合倒入三口烧瓶中,并将三口烧瓶移入数显测速恒温磁力搅拌器,于温度为85℃,转速为500r/min条件下,恒温搅拌反应12h,过滤,得滤饼湿料;再将所得滤饼湿料注入模具中,于压力为10MPa条件下压制成型后,将模具移入温度为110℃的烘箱中,干燥至恒重,脱模,得砖坯,并将所得砖坯移入烧结炉中,并以800mL/min速率向炉内通入氩气保护,于氩气保护状态下,以8℃/min速率程序升温至1500℃,保温反应4h后,停止通入氩气,并以8℃/min速率降温至1100℃,于空气气氛中,保温烧结5h,随炉冷却至室温,出料,即得轻质多孔大理石复合砖。所述正硅酸乙酯溶液是由正硅酸乙酯和无水乙醇按体积比为1:8混合而成。所述引发剂为过硫酸铵。
实例2
将大理石倒入粉碎机中,粉碎后过800目的圆孔筛,得细化大理石粉,再将细化大理石粉和无水乙醇按质量比为1:10混合后,转入超声分散仪,于超声频率为55kHz条件下,超声分散60min,得大理石分散液;按重量份数计,依次取30份正硅酸乙酯溶液,8份硼酸,0.8份纳米铁粉,6份氟化钠,100份大理石分散液,先将大理石分散液加入四口烧瓶中,并将四口烧瓶移入数显测速恒温磁力搅拌器,设定搅拌转速为600r/min,温度为60℃,再于恒温搅拌状态下,通过滴液漏斗向四口烧瓶中滴加正硅酸乙酯溶液,控制滴加速率为8mL/min,待正硅酸乙酯溶液滴加完毕,用氨水调节四口烧瓶中物料pH至9.8,继续恒温搅拌反应36h后,再向四口烧瓶中加入硼酸,纳米铁粉和氟化钠,继续搅拌混合4h后,出料,得改性大理石分散液;按重量份数计,依次取30份丙烯酰胺,8份N,N’-亚甲基双丙烯酰胺,4份引发剂,80份改性大理石分散液,混合倒入三口烧瓶中,并将三口烧瓶移入数显测速恒温磁力搅拌器,于温度为85℃,转速为500r/min条件下,恒温搅拌反应12h,过滤,得滤饼湿料;再将所得滤饼湿料注入模具中,于压力为10MPa条件下压制成型后,将模具移入温度为110℃的烘箱中,干燥至恒重,脱模,得砖坯,并将所得砖坯移入烧结炉中,并以800mL/min速率向炉内通入氩气保护,于氩气保护状态下,以8℃/min速率程序升温至1500℃,保温反应4h后,停止通入氩气,并以8℃/min速率降温至1100℃,于空气气氛中,保温烧结5h,随炉冷却至室温,出料,即得轻质多孔大理石复合砖。所述正硅酸乙酯溶液是由正硅酸乙酯和无水乙醇按体积比为1:8混合而成。所述引发剂为过硫酸铵。
实例3
将大理石倒入粉碎机中,粉碎后过800目的圆孔筛,得细化大理石粉,再将细化大理石粉和无水乙醇按质量比为1:10混合后,转入超声分散仪,于超声频率为55kHz条件下,超声分散60min,待分散结束,再加入无水乙醇质量20%的聚乙烯吡咯烷酮,并于温度为55℃,转速为500r/min条件下,恒温搅拌混合36h,出料,得大理石分散液;按重量份数计,依次取8份硼酸,0.8份纳米铁粉,6份氟化钠,100份大理石分散液,先将大理石分散液加入四口烧瓶中,并将四口烧瓶移入数显测速恒温磁力搅拌器,设定搅拌转速为600r/min,温度为60℃,恒温搅拌反应36h后,再向四口烧瓶中加入硼酸,纳米铁粉和氟化钠,继续搅拌混合4h后,出料,得改性大理石分散液;按重量份数计,依次取30份丙烯酰胺,8份N,N’-亚甲基双丙烯酰胺,4份引发剂,80份改性大理石分散液,混合倒入三口烧瓶中,并将三口烧瓶移入数显测速恒温磁力搅拌器,于温度为85℃,转速为500r/min条件下,恒温搅拌反应12h,过滤,得滤饼湿料;再将所得滤饼湿料注入模具中,于压力为10MPa条件下压制成型后,将模具移入温度为110℃的烘箱中,干燥至恒重,脱模,得砖坯,并将所得砖坯移入烧结炉中,并以800mL/min速率向炉内通入氩气保护,于氩气保护状态下,以8℃/min速率程序升温至1500℃,保温反应4h后,停止通入氩气,并以8℃/min速率降温至1100℃,于空气气氛中,保温烧结5h,随炉冷却至室温,出料,即得轻质多孔大理石复合砖。所述引发剂为过硫酸铵。
实例4
将大理石倒入粉碎机中,粉碎后过800目的圆孔筛,得细化大理石粉,再将细化大理石粉和无水乙醇按质量比为1:10混合后,转入超声分散仪,于超声频率为55kHz条件下,超声分散60min,待分散结束,再加入无水乙醇质量20%的聚乙烯吡咯烷酮,并于温度为55℃,转速为500r/min条件下,恒温搅拌混合36h,出料,得大理石分散液;按重量份数计,依次取30份正硅酸乙酯溶液,8份硼酸,100份大理石分散液,先将大理石分散液加入四口烧瓶中,并将四口烧瓶移入数显测速恒温磁力搅拌器,设定搅拌转速为600r/min,温度为60℃,再于恒温搅拌状态下,通过滴液漏斗向四口烧瓶中滴加正硅酸乙酯溶液,控制滴加速率为8mL/min,待正硅酸乙酯溶液滴加完毕,用氨水调节四口烧瓶中物料pH至9.8,继续恒温搅拌反应36h后,再向四口烧瓶中加入硼酸,继续搅拌混合4h后,出料,得改性大理石分散液;按重量份数计,依次取30份丙烯酰胺,8份N,N’-亚甲基双丙烯酰胺,4份引发剂,80份改性大理石分散液,混合倒入三口烧瓶中,并将三口烧瓶移入数显测速恒温磁力搅拌器,于温度为85℃,转速为500r/min条件下,恒温搅拌反应12h,过滤,得滤饼湿料;再将所得滤饼湿料注入模具中,于压力为10MPa条件下压制成型后,将模具移入温度为110℃的烘箱中,干燥至恒重,脱模,得砖坯,并将所得砖坯移入烧结炉中,并以800mL/min速率向炉内通入氩气保护,于氩气保护状态下,以8℃/min速率程序升温至1500℃,保温反应4h后,停止通入氩气,并以8℃/min速率降温至1100℃,于空气气氛中,保温烧结5h,随炉冷却至室温,出料,即得轻质多孔大理石复合砖。所述正硅酸乙酯溶液是由正硅酸乙酯和无水乙醇按体积比为1:8混合而成。所述引发剂为过硫酸铵。
实例5
将大理石倒入粉碎机中,粉碎后过800目的圆孔筛,得细化大理石粉,再将细化大理石粉和无水乙醇按质量比为1:10混合后,转入超声分散仪,于超声频率为55kHz条件下,超声分散60min,待分散结束,再加入无水乙醇质量20%的聚乙烯吡咯烷酮,并于温度为55℃,转速为500r/min条件下,恒温搅拌混合36h,出料,得大理石分散液;按重量份数计,依次取30份正硅酸乙酯溶液,8份硼酸,0.8份纳米铁粉,6份氟化钠,100份大理石分散液,先将大理石分散液加入四口烧瓶中,并将四口烧瓶移入数显测速恒温磁力搅拌器,设定搅拌转速为600r/min,温度为60℃,再于恒温搅拌状态下,通过滴液漏斗向四口烧瓶中滴加正硅酸乙酯溶液,控制滴加速率为8mL/min,待正硅酸乙酯溶液滴加完毕,用氨水调节四口烧瓶中物料pH至9.8,继续恒温搅拌反应36h后,再向四口烧瓶中加入硼酸,纳米铁粉和氟化钠,继续搅拌混合4h后,出料,得改性大理石分散液;按重量份数计,依次取30份丙烯酰胺,8份N,N’-亚甲基双丙烯酰胺,4份引发剂,80份改性大理石分散液,混合倒入三口烧瓶中,并将三口烧瓶移入数显测速恒温磁力搅拌器,于温度为85℃,转速为500r/min条件下,恒温搅拌反应12h,过滤,得滤饼湿料;再将所得滤饼湿料注入模具中,于压力为10MPa条件下压制成型后,将模具移入温度为110℃的烘箱中,干燥至恒重,脱模,得砖坯,并将所得砖坯移入烧结炉中,于空气气氛中,保温烧结5h,随炉冷却至室温,出料,即得轻质多孔大理石复合砖。所述正硅酸乙酯溶液是由正硅酸乙酯和无水乙醇按体积比为1:8混合而成。所述引发剂为过硫酸铵。
对比例:广东某石材工艺有限公司生产的大理石复合砖。
将实例1至5所得大理石复合砖和对比例产品进行性能检测,具体检测方法如下:
根据GB13544检测上述大理石砖的强度,具体检测结果如表1所示:
表1:性能检测表
检测内容 实例1 实例2 实例3 实例4 实例5 对比例
抗压强度/MPa 33.4 26.5 25.2 25.6 25.8 20.2
由表1检测结果可知,本发明所得轻质多孔大理石复合砖具有优异的力学性能。

Claims (4)

1.一种轻质多孔大理石复合砖的制备方法,其特征在于具体制备步骤为:
(1)将大理石粉碎,过筛,得细化大理石粉,将细化大理石粉和无水乙醇按质量比为1:8~1:10混合后,超声分散,再加入无水乙醇质量10~20%的聚乙烯吡咯烷酮,恒温搅拌混合24~36h,得大理石分散液;
(2)按重量份数计,依次取20~30份正硅酸乙酯溶液,6~8份硼酸,0.6~0.8份纳米铁粉,4~6份氟化钠,80~100份大理石分散液,将正硅酸乙酯溶液滴加至大理石分散液中,并调节pH至9.6~9.8,恒温搅拌反应24~36h后,再加入硼酸、纳米铁粉和氟化钠,继续搅拌混合2~4h,得改性大理石分散液;
(3)按重量份数计,依次取20~30份丙烯酰胺,6~8份N,N’-亚甲基双丙烯酰胺,2~4份引发剂,60~80份改性大理石分散液,混合后,加热搅拌反应8~12h,再经过滤,得滤饼湿料;
(4)将所得滤饼湿料注入模具中,压制成型后,干燥,脱模,得砖坯,并将所得砖坯于氩气保护状态下,程序升温至1400~1500℃,保温反应2~4h后,于空气气氛中,于温度为1000~1100℃烧结3~5h,冷却,出料,得轻质多孔大理石复合砖。
2.根据权利要求1所述的一种轻质多孔大理石复合砖的制备方法,其特征在于:步骤(1)所述过筛为过500~800目的圆孔筛。
3.根据权利要求1所述的一种轻质多孔大理石复合砖的制备方法,其特征在于:步骤(2)所述正硅酸乙酯溶液是由正硅酸乙酯和无水乙醇按体积比为1:5~1:8混合而成。
4.根据权利要求1所述的一种轻质多孔大理石复合砖的制备方法,其特征在于:步骤(3)所述引发剂为过硫酸铵或过硫酸钾中的任意一种。
CN201810300698.7A 2018-04-04 2018-04-04 一种轻质多孔大理石复合砖的制备方法 Active CN108395275B (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810300698.7A CN108395275B (zh) 2018-04-04 2018-04-04 一种轻质多孔大理石复合砖的制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810300698.7A CN108395275B (zh) 2018-04-04 2018-04-04 一种轻质多孔大理石复合砖的制备方法

Publications (2)

Publication Number Publication Date
CN108395275A CN108395275A (zh) 2018-08-14
CN108395275B true CN108395275B (zh) 2020-12-08

Family

ID=63099610

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810300698.7A Active CN108395275B (zh) 2018-04-04 2018-04-04 一种轻质多孔大理石复合砖的制备方法

Country Status (1)

Country Link
CN (1) CN108395275B (zh)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108947440A (zh) * 2018-08-17 2018-12-07 佛山市禅城区诺高环保科技有限公司 一种高抗裂石膏粉
CN117247269A (zh) * 2023-11-14 2023-12-19 沈阳陶然寝园有限公司 一种耐高温型复合骨灰晶石材料的制备方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101080371A (zh) * 2004-12-17 2007-11-28 第一毛织株式会社 泡沫大理石制品及其加工方法
CN102180697A (zh) * 2011-01-31 2011-09-14 山东博润工业技术有限公司 轻质高强度玄武岩陶粒及其制备方法
CN102942374A (zh) * 2012-11-18 2013-02-27 安徽工业大学 一种凝胶浇注成型坯体的脱水固化处理方法
CN107698276A (zh) * 2017-09-19 2018-02-16 常州朋悦纺织品有限公司 一种多孔碳化硅陶瓷及其制备方法
CN108192309A (zh) * 2018-04-04 2018-06-22 刘凡领 一种人造大理石的制备方法

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101080371A (zh) * 2004-12-17 2007-11-28 第一毛织株式会社 泡沫大理石制品及其加工方法
CN102180697A (zh) * 2011-01-31 2011-09-14 山东博润工业技术有限公司 轻质高强度玄武岩陶粒及其制备方法
CN102942374A (zh) * 2012-11-18 2013-02-27 安徽工业大学 一种凝胶浇注成型坯体的脱水固化处理方法
CN107698276A (zh) * 2017-09-19 2018-02-16 常州朋悦纺织品有限公司 一种多孔碳化硅陶瓷及其制备方法
CN108192309A (zh) * 2018-04-04 2018-06-22 刘凡领 一种人造大理石的制备方法

Also Published As

Publication number Publication date
CN108395275A (zh) 2018-08-14

Similar Documents

Publication Publication Date Title
CN110423063B (zh) 一种仿石材轻质透水板及其制备方法
CN108395275B (zh) 一种轻质多孔大理石复合砖的制备方法
CN101654362B (zh) 一种氧氮化硅结合碳化硅高温陶瓷材料及其制备方法
CN112939459B (zh) 一种耐磨耐腐蚀陶瓷釉料及其制备方法和应用
CN109020481A (zh) 一种高强度耐污瓷砖及其制备方法
CN101921130A (zh) 刚玉莫来石坩埚
CN111574226A (zh) 一种高密度低游离硅含量反应烧结碳化硅陶瓷材料的制备方法
CN109824340A (zh) 一种研磨介质的加工工艺
CN110204322B (zh) 一种莫来石隔热耐火砖及其制备方法
CN108424119A (zh) 一种高强度耐磨仿古砖的制备方法
CN104016629A (zh) 仿古青砖及其制造方法
CN114133212A (zh) 一体成型软石砖及其制备工艺
CN103833307A (zh) 一种耐高温加气砖及其制作方法
CN105170873A (zh) 一种新型改性型砂
CN102718510B (zh) 不烧钢包底吹氩透气砖及其制备工艺
CN111393156A (zh) 堇青石多孔陶瓷的制备方法
CN108658554A (zh) 一种铜尾矿多孔蒸压灰砂砖的制备方法
CN115259876A (zh) 一种均质莫来石纤维基多孔陶瓷的制备方法
CN111848033B (zh) 一种自密实超高强度砂浆及其制备方法
CN113087501A (zh) 一种高强度石英陶瓷辊及其制备工艺
CN106187249B (zh) 一种高热稳定性的电热陶瓷及其制备工艺
CN112341080A (zh) 一种新型仿石材生态透水砖及其制备方法
CN112456985A (zh) 一种用于热风炉的低蠕变管道砖及其制备方法
CN116444287B (zh) 一种发泡陶瓷生产工艺及设备
CN110683857A (zh) 一种加气混凝土及其制备方法

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
TA01 Transfer of patent application right
TA01 Transfer of patent application right

Effective date of registration: 20201119

Address after: Room 620-660, building 3, No. 8, Tongyang Road, Suchen Town, Hailing District, Taizhou City, Jiangsu Province 225300

Applicant after: Taizhou Fengfei Machinery Equipment Co.,Ltd.

Address before: 213000 room 2902, Linglong garden, Xinbei District, Changzhou, Jiangsu, China, 1

Applicant before: Liu Fanling

GR01 Patent grant
GR01 Patent grant
TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20240429

Address after: 277000 meters east of Kangzhuang Village, Dege Town, Yicheng District, Zaozhuang City, Shandong Province (formerly within the Wulin Gypsum Mine)

Patentee after: Zaozhuang Xinwoyan Building Materials Co.,Ltd.

Country or region after: China

Address before: Room 620-660, Building 3, No. 8, Tongyang Road, Suchen Town, Hailing District, Taizhou City, Jiangsu Province 225300 (A0043 in Juwang Youcai Business Secretary (Taizhou) Co., Ltd.)

Patentee before: Taizhou Fengfei Machinery Equipment Co.,Ltd.

Country or region before: China