CN103896516A - 石材外壳及其制造方法 - Google Patents
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Abstract
本发明提供一种石材外壳,该石材外壳的材质为铁丸石,该铁丸石的主要成分为石英、粘土矿及含铁钙聚合体,所述粘土矿中含有Zn元素、Al2O3、CaO、MgO、Ba2O3、SiO2及TiO2,所述含铁钙聚合体中含有Fe2O3、Fe4O3、CaCO3及CaSiO4,该石材外壳采用铁丸石粉末为原料以注塑成型的方式制成。本发明还提供一种石材外壳的制造方法。
Description
技术领域
本发明涉及一种石材外壳及其制造方法。
背景技术
现有的电子产品壳体的材质主要为金属、塑料及玻璃。但,由于金属壳体易于被腐蚀性介质腐蚀,使金属壳体表面的装饰性膜层发生脱落,严重影响其外观;塑料基体的抗老化性能较差;而玻璃壳体易碎且难以形成复杂的三维结构。此外,上述三种材质的壳体均不具有如玉石般温润、细腻的手感。
发明内容
有鉴于此,提供一种具有良好的抗老化性、耐腐蚀性及硬度的石材外壳。
另,还提供一种上述石材外壳的制造方法。
一种石材外壳,该石材外壳的材质为铁丸石,该铁丸石的主要成分为石英、粘土矿及含铁钙聚合体,所述粘土矿中含有Zn元素、Al2O3、CaO、MgO、Ba2O3、SiO2及TiO2,所述含铁钙聚合体中含有Fe2O3、Fe4O3、CaCO3及CaSiO4,该石材外壳采用铁丸石粉末为原料以注塑成型的方式制成。
一种石材外壳的制造方法,其包括如下步骤:
提供一铁丸石粉末,该铁丸石粉末的主要成分为石英、粘土矿及含铁钙聚合体,所述粘土矿中含有Zn元素、Al2O3、CaO、MgO、Ba2O3、SiO2及TiO2,所述含铁钙聚合体中含有Fe2O3、Fe4O3、CaCO3及CaSiO4;
将铁丸石粉末、胶粘剂及增塑剂混合,经混料机造料制得注塑料,该胶粘剂为聚乙烯及聚丙烯的混合物,增塑剂为邻苯二甲酸二丁酯;
采用所述注塑料进行注塑成型,成型一坯体;
对所述坯体进行脱脂处理;
对坯体进行烧结处理,制得石材外壳。
本发明采用铁丸石粉末为原料经注塑成型制造所述石材外壳,使所述石材外壳具有温润、细腻的手感,同时具有良好的耐腐蚀性及抗老化性能。
具体实施方式
本发明一较佳实施例的石材外壳可以是手机、PDA、笔记本电脑、MP3、MP4、GPS导航仪、蓝牙耳机、数码相机及音箱等产品的外壳。
该石材外壳的材质为铁丸石。该铁丸石的主要成分为石英(SiO2)、粘土矿及含铁钙聚合体。此外,铁丸石还含有少量的碳化物、氧化镍及氧化铅等杂质。该铁丸石中,石英的质量百分含量为51~62%、粘土矿的质量百分含量为27~34%、含铁钙聚合体的质量百分含量为8~10%、及所述杂质的质量百分含量为3~5%。所述粘土矿为高岭石﹑蒙脱石﹑方解石、云母及伊利石等。该粘土矿中含有Zn元素及Al2O3、CaO、MgO、Ba2O3、SiO2、TiO2等氧化物。所述含铁钙聚合体中含有Fe2O3、Fe4O3、CaCO3及CaSiO4。
本发明一较佳实施例的石材外壳的制造方法,主要包括如下步骤:
(1)提供铁丸石粉末。
所述铁丸石粉末的粒径为0.4~0.1mm。该铁丸石的主要成分为石英(SiO2)、粘土矿及含铁钙聚合体。此外,铁丸石还含有少量的碳化物、氧化镍及氧化铅等杂质。该铁丸石中,石英的质量百分含量为51~62%、粘土矿的质量百分含量为27~34%、含铁钙聚合体的质量百分含量为8~10%、及所述杂质的质量百分含量为3~5%。所述粘土矿为高岭石﹑蒙脱石﹑方解石、云母及伊利石等。该粘土矿中含有Zn元素及Al2O3、CaO、MgO、Ba2O3、SiO2、TiO2等氧化物。所述含铁钙聚合体中含有Fe2O3、Fe4O3、CaCO3及CaSiO4。
(2)制造注塑料。
将铁丸石粉末、胶粘剂及增塑剂以(42~47):(35~50):(3~8)的体积比配制并置于混料机内,之后在140~180℃的温度下混合60~150min,制得注塑料。该胶粘剂为聚乙烯(PE)及聚丙烯(PP)的混合物。增塑剂为邻苯二甲酸二丁酯(DBP)。所述注塑料为柱状体,长为4~7mm,直径为2~3mm。
(3)采用所述注塑料进行注塑成型,成型一坯体。
所述注塑成型的压力为120~180MPa,注射温度为150~170℃,模具温度为40~60℃;之后,进行保压处理形成一坯体,保压压力为200~300MPa,保压时间为20~50min。
(4)对所述坯体进行脱脂处理。
将所述坯体置于一脱脂炉中,将脱脂炉内的温度以25~37℃/h的升温速率由室温升至150℃;再以3.8~6.3℃/h的升温速率升至400℃;之后,以6.6~10℃/h的升温速率升至500℃;最后,以29.2~50℃/h的升温速率升至850℃。所述脱脂处理用以脱除坯体中的增塑剂及粘结剂。脱脂处理后,将所述坯体自然冷却至室温。
(5)对坯体进行烧结处理。
将脱脂后的坯体置于一烧结炉中,将烧结炉内的温度经梯度升温至1250℃,具体操作及工艺参数如下:先以4~6℃/min的升温速率由室温升至600℃;再以2~4℃/min的升温速率升至800℃;最后,以0.8~1.2℃/min的升温速率升至1250℃,并在该温度下保温时间为90~150min。之后,再对所述坯体进行降温处理,具体操作及工艺参数如下:先以3.7~5℃/min的降温速率将烧结炉内的温度降至800℃,再以3.7~5℃/min的降温速率将烧结炉内的温度降至室温。
(6)采用CNC铣削或激光切割处理,将坯体加工成预定尺寸的石材壳体。
(7)对石材壳体研磨或抛光处理。
所述研磨或抛光处理用以提高石材壳体表面的平整度。
(8)清洗所述石材壳体。
所述清洗处理包括如下步骤:先采用pH值为5的弱酸溶液清洗5~15分钟,去除坯体表面的碱性杂质;再采用pH值为9的弱碱溶液清洗5~15分钟,去除坯体表面的酸性杂质;之后,采用10wt%的乙醇或丙酮清洗5~15分钟,去除坯体表面的有机杂质,纯水清洗5分钟;最后,将坯体置于60~80℃温度下干燥40~80min。本实施例中,所述弱酸溶液为盐酸溶液,所述碱性溶液为氢氧化钠溶液。
本发明采用铁丸石粉末为原料经注塑成型制造所述石材外壳,使所述石材外壳具有温润、细腻的手感,同时具有良好的耐腐蚀性及抗老化性能。另外,采用该铁丸石粉末添加胶粘剂及增塑剂进行注塑成型该石材外壳,相较于现有单纯的机械磨削制程,效率高,成本低,且较容易获得三维结构的石材外壳。
Claims (10)
1.一种石材外壳,其特征在于:该石材外壳的材质为铁丸石,该铁丸石的主要成分为石英、粘土矿及含铁钙聚合体,所述粘土矿中含有Zn元素、Al2O3、CaO、MgO、Ba2O3、SiO2及TiO2,所述含铁钙聚合体中含有Fe2O3、Fe4O3、CaCO3及CaSiO4,该石材外壳采用铁丸石粉末为原料以注塑成型的方式制成。
2.如权利要求1所述的石材外壳,其特征在于:该铁丸石中,石英的质量百分含量为51~62%、粘土矿的质量百分含量为27~34%、含铁钙聚合体的质量百分含量为8~10%。
3.如权利要求1所述的石材外壳,其特征在于:该粘土矿为高岭石﹑蒙脱石﹑方解石、云母及伊利石。
4.一种石材外壳的制造方法,其包括如下步骤:
提供一铁丸石粉末,该铁丸石粉末的主要成分为石英、粘土矿及含铁钙聚合体,所述粘土矿中含有Zn元素、Al2O3、CaO、MgO、Ba2O3、SiO2及TiO2,所述含铁钙聚合体中含有Fe2O3、Fe4O3、CaCO3及CaSiO4;
将铁丸石粉末、胶粘剂及增塑剂混合,经混料机造料制得注塑料,该胶粘剂为聚乙烯及聚丙烯的混合物,增塑剂为邻苯二甲酸二丁酯;
采用所述注塑料进行注塑成型,成型一坯体;
对所述坯体进行脱脂处理;
对坯体进行烧结处理,制得石材外壳。
5.如权利要求4所述的石材外壳的制造方法,其特征在于:所述脱脂处理的方法为:先将脱脂炉内的温度以25~37℃/h的升温速率由室温升至150℃;再以3.8~6.3℃/h的升温速率升至400℃;之后,以6.6~10℃/h的升温速率升至500℃;最后,以29.2~50℃/h的升温速率升至850℃。
6.如权利要求4所述的石材外壳的制造方法,其特征在于:该烧结处理包括如下步骤:先将坯体置于一烧结炉中;再将该烧结炉内的温度升温至1250℃;之后,对该烧结炉进行降温处理。
7.如权利要求6所述的石材外壳的制造方法,其特征在于:该烧结过程中通过如下方法将烧结炉内的升温至1250℃:先以4~6℃/min的升温速率由室温升至600℃;再以2~4℃/min的升温速率升至800℃;最后,以0.8~1.2℃/min的升温速率升至1250℃,并在该温度下保温时间为90~150min。
8.如权利要求6所述的石材外壳的制造方法,其特征在于:所述降温处理的方法为:先以3.7~5℃/min的降温速率将烧结炉内的温度降至800℃,再以3.7~5℃/min的降温速率将烧结炉内的温度降至室温。
9.如权利要求4所述的石材外壳的制造方法,其特征在于:采用所述注塑料进行注塑成型的压力为120~180MPa,注射温度为150~170℃,模具温度为40~60℃。
10.如权利要求4所述的石材外壳的制造方法,其特征在于:注塑料通过如下方法制得:将铁丸石粉末、胶粘剂及增塑剂以(42~47):(35~50):(3~8)的体积比置于混料机内,并在140~180℃的温度下混合60~150min。
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TW102103189A TW201433237A (zh) | 2012-12-29 | 2013-01-28 | 石材外殼及其製造方法 |
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US4321158A (en) * | 1980-05-30 | 1982-03-23 | The United States Of America As Represented By The United States Department Of Energy | Backfill composition for secondary barriers in nuclear waste repositories |
DE3821341A1 (de) * | 1988-06-24 | 1989-12-28 | Bayer Ag | Neue hitzestabile eisenoxidschwarz-pigmente, verfahren zu ihrer herstellung sowie deren verwendung |
US7741397B2 (en) * | 2004-03-17 | 2010-06-22 | Dow Global Technologies, Inc. | Filled polymer compositions made from interpolymers of ethylene/α-olefins and uses thereof |
US7093529B2 (en) * | 2004-10-14 | 2006-08-22 | Delaware Capital Formation, Inc. | Composite piston |
KR101191370B1 (ko) * | 2005-04-04 | 2012-10-15 | 헨켈 아게 운트 코. 카게아아 | 방사선 경화성 건조제-충전 접착제/밀봉제 |
US20090099299A1 (en) * | 2006-11-22 | 2009-04-16 | Robert Russell Gallucci | Polymer blend compositions |
-
2012
- 2012-12-29 CN CN201210590270.3A patent/CN103896516A/zh active Pending
-
2013
- 2013-01-28 TW TW102103189A patent/TW201433237A/zh unknown
- 2013-06-28 US US13/930,306 patent/US20140184039A1/en not_active Abandoned
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US20140184039A1 (en) | 2014-07-03 |
TW201433237A (zh) | 2014-08-16 |
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