CN111663166B - 一种氮化硅纳米银复合电沉积涂层及其制备方法与应用 - Google Patents
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- 239000002131 composite material Substances 0.000 title claims abstract description 20
- 229910052581 Si3N4 Inorganic materials 0.000 title claims abstract description 19
- 238000004070 electrodeposition Methods 0.000 title claims abstract description 15
- 238000002360 preparation method Methods 0.000 title claims abstract description 8
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 title abstract description 4
- 238000010008 shearing Methods 0.000 claims abstract description 17
- 239000000243 solution Substances 0.000 claims abstract description 16
- 125000002091 cationic group Chemical group 0.000 claims abstract description 14
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- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 5
- 238000005260 corrosion Methods 0.000 claims description 4
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- 239000002245 particle Substances 0.000 claims description 4
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 claims description 3
- 239000004697 Polyetherimide Substances 0.000 claims description 3
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- 229910001200 Ferrotitanium Inorganic materials 0.000 claims description 2
- 229910001069 Ti alloy Inorganic materials 0.000 claims description 2
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- -1 alkyl dimethyl benzyl ammonium chloride Chemical compound 0.000 claims description 2
- 239000010405 anode material Substances 0.000 claims description 2
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- 239000002114 nanocomposite Substances 0.000 abstract description 2
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000009713 electroplating Methods 0.000 description 2
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- 238000006467 substitution reaction Methods 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 208000017667 Chronic Disease Diseases 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 230000006196 deacetylation Effects 0.000 description 1
- 238000003381 deacetylation reaction Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- ZNCPFRVNHGOPAG-UHFFFAOYSA-L sodium oxalate Chemical compound [Na+].[Na+].[O-]C(=O)C([O-])=O ZNCPFRVNHGOPAG-UHFFFAOYSA-L 0.000 description 1
- 229940039790 sodium oxalate Drugs 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D15/00—Electrolytic or electrophoretic production of coatings containing embedded materials, e.g. particles, whiskers, wires
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- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
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Abstract
本发明属于氮化硅纳米复合表面涂层制备技术领域,具体公开了一种Si3N4纳米银复合电沉积涂层及其制备方法与应用。步骤为:(1)将壳聚糖溶液与其他阳离子分散剂混合均匀,然后依次加入Si3N4粉和纳米银得到混合溶液;(2)将所得混合溶液经剪切分散得到纳米悬浮液,然后调节pH至中性;(3)将阴极和阳极电极材料放入所得纳米悬浮溶液中;并通入直流电,沉积得到Si3N4纳米银复合涂层;本发明提供的Si3N4纳米银复合电沉积涂层,可以代替电镀铬涂层。该涂层制备简单快捷,环保无污染,且制备涂层对于基底材料有良好的保护作用,提高材料耐磨性能,解决特异构件镀层问题。
Description
技术领域
本发明属于氮化硅(Si3N4)纳米复合表面涂层制备技术领域,特别涉及一种Si3N4纳米银复合电沉积涂层及其制备方法与应用。
背景技术
电镀铬涂层因光洁度好、硬度高、耐磨耐蚀性强等优势,国内许多重要工业领域仍大量应用。但电镀铬工艺引发的环境污染、危害健康等问题,已成为制约我国建设环境友好型社会的顽疾。替代电镀铬的绿色表面处理技术为解决上述难题提供了突破口,但目前国内在车辆交通、钢铁、矿山等重大行业诸多典型部件仍缺失该类绿色技术。
发明内容
为了克服上述现有技术的缺点与不足,本发明的首要目的在于提供一种Si3N4纳米银复合电沉积涂层的制备方法。
本发明另一目的在于提供上述方法制备得到的Si3N4纳米银复合电沉积涂层。
本发明再一目的在于提供上述Si3N4纳米银复合电沉积涂层在耐摩擦防腐蚀部件中的应用。
本发明的目的通过下述方案实现:
一种Si3N4纳米银复合电沉积涂层的制备方法,包括以下步骤:
(1)将阳离子分散剂A与阳离子分散剂B混合均匀,然后依次加入Si3N4粉和纳米银得到混合溶液;
(2)将步骤(1)所得混合溶液经剪切分散得到纳米悬浮液,然后调节pH至中性;
(3)将阴极和阳极电极材料放入步骤(2)所得纳米悬浮溶液中;并通入直流电,沉积得到Si3N4纳米银复合涂层;
其中步骤(1)所述阳离子分散剂A为壳聚糖溶液,阳离子分散剂B为十六烷基三甲基溴化铵(CTAB)、聚醚酰亚胺(PEI)和烷基二甲基苄基氯化铵(ADBAC)中的至少一种;
所述阳离子分散剂B与阳离子分散剂A的质量体积比为0.02g:20~25mL。
步骤(1)所述壳聚糖溶液的浓度为0.1%~0.4%wt;优选为0.2%wt。
步骤(1)所述混合溶液中Si3N4粉的浓度为10-20g/L,粒径为0.5~3微米;纳米银的浓度为1-2g/L,粒径为50-100nm。
步骤(2)所述剪切分散在剪切分散机中进行,剪切分散的条件为:剪切分散机转速为300-500r/min,剪切分散5-10min后调整转速1500-2000r/min,再剪切分散10-15min。
步骤(2)所述条件pH至中性所用的试剂为本领域常用试剂,优选为NaOH、柠檬酸、柠檬酸钠、甲酸、尿素、草酸钠和溴化铵中的至少一种。
步骤(3)所述阴极材料为钛合金、纯钛或不锈钢;优选地,在使用阴极材料前,先对其进行清洗,具体为抛光去油,然后用HF溶液擦拭表面。所述阳极材料为常用惰性电极,优选为石墨或铂片。
步骤(3)所述阴极与阳极在纳米悬浮溶液中的间距为1-2cm。步骤(3)所述直流电的施加电压范围为10-60V,电流密度为0.01-0.5mA/cm2。
步骤(3)所述沉积时间为1-5min。优选地,通入直流电进行沉积前,对纳米悬浮溶液搅拌10~30min。
一种Si3N4纳米银复合电沉积涂层通过上述方法制备得到。
所述Si3N4纳米银复合电沉积涂层在耐摩擦防腐蚀部件中的应用。
本发明相对于现有技术,具有如下的优点及有益效果:
本发明提供的Si3N4纳米银复合电沉积涂层,可以代替电镀铬涂层。该涂层制备简单快捷,环保无污染,且制备涂层对于基底材料有良好的保护作用,提高材料耐磨性能,解决特异构件镀层问题。
具体实施方式
下面结合实施例对本发明作进一步详细的描述,但本发明的实施方式不限于此。
实施例中所用试剂如无特殊说明均可从市场常规购得。壳聚糖的脱乙酰度为85%-95%。
实施例1-12中Si3N4纳米银复合涂层采用以下方法制得:
(1)壳聚糖溶液:将0.5g壳聚糖、0.25mL冰乙酸和247.5mL去离子水混合后,搅拌溶解7h以上,得到壳聚糖溶液。
(2)将上述壳聚糖溶液与0.02g阳离子分散剂混合均匀,然后加入1g Si3N4粉(1-2μm)和0.05g纳米银(50-100nm),再加入乙醇25mL得到混合溶液;
(3)将步骤(2)所得混合溶液放置在剪切分散机上,剪切分散机转速为300-500r/min,剪切分散5-10min后调整转速1500-2000r/min,继续剪切分散10-15min得到纳米悬浮液,然后调节pH至7.14;
(4)将阴极和阳极(Pt)电极材料放入步骤(3)所得pH=7.14的纳米悬浮溶液中,电极间距1-2cm;并通入直流电,施加电压40V,电流密度0.01-0.5mA/cm2,沉积1-5min得到Si3N4纳米银复合涂层。
表1实施例1~12的条件参数及所得涂层的性能
上述实施例为本发明较佳的实施方式,但本发明的实施方式并不受上述实施例的限制,其他的任何未背离本发明的精神实质与原理下所作的改变、修饰、替代、组合、简化,均应为等效的置换方式,都包含在本发明的保护范围之内。
Claims (9)
1.一种Si3N4纳米银复合电沉积涂层的制备方法,其特征在于包括以下步骤:
(1)将阳离子分散剂A与阳离子分散剂B混合均匀,然后依次加入Si3N4粉和纳米银得到混合溶液;
(2)将步骤(1)所得混合溶液经剪切分散得到纳米悬浮液,然后调节pH至中性;
(3)将阴极和阳极电极材料放入步骤(2)所得纳米悬浮溶液中;并通入直流电,沉积得到Si3N4纳米银复合涂层;
其中步骤(1)所述阳离子分散剂A为壳聚糖溶液,阳离子分散剂B为十六烷基三甲基溴化铵、聚醚酰亚胺和烷基二甲基苄基氯化铵中的至少一种;所述阳离子分散剂B与阳离子分散剂A的质量体积比为0.02g:20~25mL;
步骤(3)所述直流电的施加电压范围为10-60V,电流密度为0.01-0.5mA/cm2;
步骤(1)所述壳聚糖溶液的浓度为0.1%~0.4%wt。
2.根据权利要求1所述的方法,其特征在于:
步骤(1)所述混合溶液中Si3N4粉的浓度为10-20g/L,纳米银的浓度为1-2g/L。
3.根据权利要求1所述的方法,其特征在于:步骤(1)所述混合溶液中Si3N4粉的粒径为0.5~3微米;纳米银的粒径为50-100 nm。
4.根据权利要求1或2或3所述的方法,其特征在于:步骤(2)所述剪切分散在剪切分散机中进行,剪切分散的条件为:剪切分散机转速为300-500r/min,剪切分散5-10min后调整转速1500-2000r/min,再剪切分散10-15min。
5.根据权利要求1所述的方法,其特征在于:步骤(3)所述阴极与阳极在纳米悬浮溶液中的间距为1-2cm。
6.根据权利要求1所述的方法,其特征在于:步骤(3)所述沉积时间为1-5min。
7.根据权利要求1所述的方法,其特征在于:步骤(3)所述阴极材料为钛合金、纯钛或不锈钢;所述阳极材料为石墨或铂片。
8.一种Si3N4纳米银复合电沉积涂层通过权利要求1~7任一项所述方法制备得到。
9.根据权利要求8所述Si3N4纳米银复合电沉积涂层在耐摩擦防腐蚀部件中的应用。
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