CN115364639B - 一种水基量子点除醛功能添加剂及其制备方法 - Google Patents
一种水基量子点除醛功能添加剂及其制备方法 Download PDFInfo
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- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 title claims abstract description 147
- 239000002096 quantum dot Substances 0.000 title claims abstract description 54
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 47
- 239000013538 functional additive Substances 0.000 title claims abstract description 36
- 238000002360 preparation method Methods 0.000 title claims abstract description 28
- 108010010803 Gelatin Proteins 0.000 claims abstract description 46
- 229920000159 gelatin Polymers 0.000 claims abstract description 46
- 239000008273 gelatin Substances 0.000 claims abstract description 46
- 235000019322 gelatine Nutrition 0.000 claims abstract description 46
- 235000011852 gelatine desserts Nutrition 0.000 claims abstract description 46
- 239000000243 solution Substances 0.000 claims abstract description 38
- 239000007864 aqueous solution Substances 0.000 claims abstract description 22
- 238000003756 stirring Methods 0.000 claims abstract description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 20
- 238000010438 heat treatment Methods 0.000 claims abstract description 18
- 239000000654 additive Substances 0.000 claims abstract description 16
- 230000000996 additive effect Effects 0.000 claims abstract description 16
- CTENFNNZBMHDDG-UHFFFAOYSA-N Dopamine hydrochloride Chemical compound Cl.NCCC1=CC=C(O)C(O)=C1 CTENFNNZBMHDDG-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229960001149 dopamine hydrochloride Drugs 0.000 claims abstract description 14
- 229910000033 sodium borohydride Inorganic materials 0.000 claims abstract description 12
- 239000012279 sodium borohydride Substances 0.000 claims abstract description 12
- -1 sodium tetrahydroborate Chemical compound 0.000 claims abstract description 12
- 238000001816 cooling Methods 0.000 claims abstract description 11
- 229910052751 metal Inorganic materials 0.000 claims abstract description 11
- 239000002184 metal Substances 0.000 claims abstract description 11
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 10
- 239000002244 precipitate Substances 0.000 claims abstract description 10
- 238000000926 separation method Methods 0.000 claims abstract description 10
- 239000012266 salt solution Substances 0.000 claims abstract description 8
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 claims description 9
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 8
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 claims description 8
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 8
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims description 8
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims description 8
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims description 8
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 claims description 8
- 239000003223 protective agent Substances 0.000 claims description 8
- 239000003381 stabilizer Substances 0.000 claims description 8
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 claims description 7
- 239000000661 sodium alginate Substances 0.000 claims description 7
- 235000010413 sodium alginate Nutrition 0.000 claims description 7
- 229940005550 sodium alginate Drugs 0.000 claims description 7
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 4
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 claims description 3
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052901 montmorillonite Inorganic materials 0.000 claims description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 2
- 229910002651 NO3 Inorganic materials 0.000 claims description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 2
- 229910010413 TiO 2 Inorganic materials 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- 239000007921 spray Substances 0.000 abstract description 19
- 239000000839 emulsion Substances 0.000 abstract description 13
- 239000003973 paint Substances 0.000 abstract description 13
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 8
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- 229910021641 deionized water Inorganic materials 0.000 description 6
- 230000001105 regulatory effect Effects 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 4
- 102000004190 Enzymes Human genes 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 3
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- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 2
- 206010028980 Neoplasm Diseases 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
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- VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 description 2
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- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000011056 performance test Methods 0.000 description 2
- 239000011941 photocatalyst Substances 0.000 description 2
- 231100000719 pollutant Toxicity 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- 208000003174 Brain Neoplasms Diseases 0.000 description 1
- 208000014085 Chronic respiratory disease Diseases 0.000 description 1
- 206010009944 Colon cancer Diseases 0.000 description 1
- 206010011224 Cough Diseases 0.000 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- 208000002454 Nasopharyngeal Carcinoma Diseases 0.000 description 1
- 206010061306 Nasopharyngeal cancer Diseases 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229910021446 cobalt carbonate Inorganic materials 0.000 description 1
- ZOTKGJBKKKVBJZ-UHFFFAOYSA-L cobalt(2+);carbonate Chemical compound [Co+2].[O-]C([O-])=O ZOTKGJBKKKVBJZ-UHFFFAOYSA-L 0.000 description 1
- 208000029742 colonic neoplasm Diseases 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229960003638 dopamine Drugs 0.000 description 1
- 238000011841 epidemiological investigation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 231100000869 headache Toxicity 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 208000030603 inherited susceptibility to asthma Diseases 0.000 description 1
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 description 1
- 229910000360 iron(III) sulfate Inorganic materials 0.000 description 1
- 208000032839 leukemia Diseases 0.000 description 1
- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 description 1
- 201000011216 nasopharynx carcinoma Diseases 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 1
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 239000002957 persistent organic pollutant Substances 0.000 description 1
- PQTLYDQECILMMB-UHFFFAOYSA-L platinum(2+);sulfate Chemical compound [Pt+2].[O-]S([O-])(=O)=O PQTLYDQECILMMB-UHFFFAOYSA-L 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000000241 respiratory effect Effects 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
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Abstract
本发明涉及除甲醛技术领域,具体而言,涉及一种水基量子点除醛功能添加剂及其制备方法,包括以下步骤:S1.向含有明胶的量子点金属盐溶液中通入氮气,搅拌、升温后,滴加盐酸多巴胺及四氢硼钠水溶液,滴加完毕后,调节溶液PH值至11‑13,反应一段时间;S2.将反应后的溶液冷却后,加入改性明胶水溶液,搅拌后,高速离心分离,去除上层溶液,沉淀物经分散后即得水基量子点除醛添加剂;本发明制备得到的添加剂具有很好的水溶性,更容易添加到水性除醛喷剂、乳胶漆等中,并可在除醛喷剂或乳胶漆体系中分散的更均匀。
Description
技术领域
本发明涉及除甲醛技术领域,具体而言,涉及一种水基量子点除醛功能添加剂及其制备方法。
背景技术
甲醛是一种高挥发性的有机污染物。尤其是在室内装修中材料会释放多种气态污染物污染室内环境,其中的甲醛就是最典型、危害最大的污染物之一。甲醛在室内的含量越来越高,远大于室外空气中甲醛的浓度。长期接触甲醛容易引起慢性呼吸道疾病、鼻咽癌、结肠癌、脑癌、白血病等疾病。根据流行病学调查表明,非工业环境的人群(如室内居民)长期暴露在低浓度甲醛环境下,会发生眼部刺激、上呼吸道刺激、头痛和咳嗽等症状。如果长期吸入高浓度甲醛气体,还可能引发支气管哮喘,甚至会导致人体肿瘤与癌症。
目前用的除甲醛的方法主要有以下几种:(一)生物酶法。通过微生物的繁衍生产生物酶,在微生物和生物酶的双重作用下,可以将甲醛分解为二氧化碳和水,该方法有效时间较短,持续性较弱。(二)光触媒法。通过可见光活化的光触媒能够在有光线的地方持续不断地分解甲醛。氧化钛具有高的催化活性、良好的稳定性、能够降解有机污染物以及廉价无毒等优点,因此广泛应用于涂料添加剂用于去除其中的甲醛。然而,在涂料添加除醛应用中,基于氧化钛的光降解材料只能在紫外线下有较高的效率,在可见光下效率低下,严重限制氧化钛的应用。
发明内容
发明人考虑到室内环境同时存在的除甲醛和杀菌的实际需要,本发明意在合成一种新型的具有与甲醛快速反应的甲醛清除剂,不受紫外线照射应用条件限制,在可见光环境下也具有良好反应活性的除醛添加剂。
本发明发明人提出了利用量子点表面的活性键可与甲醛及有机溶剂反应,从而有效消除空气中的甲醛及TVOC的构思,本发明的目的在于提供一种水基量子点除醛功能添加剂的制备方法,制备得到的添加剂具有很好的水溶性,更容易添加到水性除醛喷剂、乳胶漆等中,并可在除醛喷剂或乳胶漆体系中分散的更均匀。
本发明的实施例通过以下技术方案实现:
一种水基量子点除醛功能添加剂的制备方法,包括以下步骤:
S1.向含有明胶的量子点金属盐溶液中通入氮气,搅拌、升温后,滴加盐酸多巴胺及四氢硼钠水溶液,滴加完毕后,调节溶液PH值至11-13,反应一段时间;
S2.将反应后的溶液冷却后,加入改性明胶水溶液,搅拌后,高速离心分离,去除上层溶液,沉淀物经分散后即得水基量子点除醛添加剂。
一种量子点除醛功能添加剂,由上述的水基量子点除醛功能添加剂的制备方法制得。
本发明实施例的技术方案至少具有如下优点和有益效果:
本发明水基量子点除醛功能添加剂的制备方法制备得到的添加剂具有很好的水溶性,更容易添加到水性除醛喷剂、乳胶漆等中,并可在除醛喷剂或乳胶漆体系中分散的更均匀;除此之外,本发明制备得到的除醛添加剂可减少纳米量子点金属颗粒的团聚,使得最终制得的除醛功能添加剂添加到除醛喷剂、乳胶漆等中后,除醛喷剂、乳胶漆的除醛效果更充分。
具体实施方式
为使本发明实施例的目的、技术方案和优点更加清楚,下面将对本发明实施例中的技术方案进行清楚、完整地描述。实施例中未注明具体条件者,按照常规条件或制造商建议的条件进行。所用试剂或仪器未注明生产厂商者,均为可以通过市售购买获得的常规产品。
下面对本发明实施例提供的一种量子点除醛功能添加剂及其制备方法进行具体说明。
一种水基量子点除醛功能添加剂的制备方法,包括以下步骤:
S1.向含有明胶的量子点金属盐溶液中通入氮气,搅拌、升温后,滴加盐酸多巴胺及四氢硼钠水溶液,滴加完毕后,调节溶液PH值至11-13,反应一段时间;本发明提出了利用量子点表面的活性键可与甲醛及有机溶剂反应,从而有效消除空气中的甲醛及TVOC等的构思;并且本发明利用多巴胺的粘附效应,能够附着并包覆于所制得的纳米量子点金属表面,从而减少所得的纳米量子点金属颗粒的团聚,使得最终制得的除醛功能添加剂添加到除醛喷剂、乳胶漆等中后,除醛喷剂、乳胶漆的除醛效果更充分;
S2.将反应后的溶液冷却后,加入改性明胶水溶液,搅拌后,高速离心分离,去除上层溶液,沉淀物经分散后即得水基量子点除醛添加剂;这样可使得除醛功能添加剂具有疏松多孔的结构,具有很好的水溶性,从而有利于添加到除醛喷剂、乳胶漆等中后分散的更均匀,提高除醛效果。
进一步地,S2中,所述改性明胶包括明胶和载体,所述载体包括SiO2、CaCO3、TiO2、蒙脱土或滑石粉中的一种或几种,具有很强的吸附能力和孔隙率,从而在添加到除醛喷剂、乳胶漆等中后,可更稳定地吸附于除醛喷剂、乳胶漆体系中,并可高效地吸附空气中的甲醛等有害物质。
进一步地,所述改性明胶的制备方法为:将5%的载体溶液分散于1%的明胶中,并加入羟丙基甲基纤维素或海藻酸钠为保护剂、十六烷基三甲基溴化铵、十二烷基苯磺酸钠作为稳定剂,加热后即得。
进一步地,S1中,所述量子点金属盐包括Ni、Co、Fe、Ag、Mn、Zn、Pt、Au的硫酸盐、碳酸盐、硝酸盐、氯酸盐中的一种或几种。
进一步地,S1中,所述含有明胶的量子点金属盐溶液为含有1-3%明胶的0.1-0.5mol/L的量子点金属盐溶液。
进一步地,S1中,搅拌速率为100-150r/min,升温至30-60℃。
进一步地,S1中,所述盐酸多巴胺的浓度为1-5g/L,四氢硼钠水溶液的浓度为0.01-0.1mol/L。
进一步地,S1中采用30%的氨水调节溶液PH。
进一步地,所述S2中冷却至20-40℃。
一种量子点除醛功能添加剂,由上述水基量子点除醛功能添加剂的制备方法制得。
实施例1
一种水基量子点除醛功能添加剂的制备方法,包括以下步骤:
向含有1%明胶的0.2mol/L的硫酸锌溶液中通入氮气,120r/min下搅拌,升温至40℃后,滴加3g/L的盐酸多巴胺及0.05mol/L的四氢硼钠水溶液,滴加完毕后,采用30%的氨水调节溶液PH值至12,反应3h,反应完成后,将反应后的溶液冷却至25℃,加入含5%的SiO2改性的明胶(1%)水溶液,搅拌2h后停止反应,高速离心分离,去除上层溶液,沉淀物用50mL去离子水分散后即得水基量子点除醛添加剂;其中,改性明胶的制备方法为:将5%的载体溶液分散于1%的明胶中,并加入羟丙基甲基纤维素或海藻酸钠为保护剂,十六烷基三甲基溴化铵、十二烷基苯磺酸钠作为稳定剂,加热后即得。
实施例2
一种水基量子点除醛功能添加剂的制备方法,包括以下步骤:
向含有1%明胶的0.1mol/L的硫酸镍溶液中通入氮气,100r/min下搅拌,升温至30℃后,滴加1g/L的盐酸多巴胺及0.01mol/L的四氢硼钠水溶液,滴加完毕后,采用30%的氨水调节溶液PH值至11,反应3h,反应完成后,将反应后的溶液冷却至20℃,加入含5%的SiO2改性的明胶(1%)水溶液,搅拌2h后停止反应,高速离心分离,去除上层溶液,沉淀物用50mL去离子水分散后即得水基量子点除醛添加剂;其中,改性明胶的制备方法为:将5%的载体溶液分散于1%的明胶中,并加入羟丙基甲基纤维素或海藻酸钠为保护剂、十六烷基三甲基溴化铵、十二烷基苯磺酸钠作为稳定剂,加热后即得。
实施例3
一种水基量子点除醛功能添加剂的制备方法,包括以下步骤:
向含有3%明胶的0.5mol/L的硝酸银溶液中通入氮气,150r/min下搅拌,升温至60℃后,滴加5g/L的盐酸多巴胺及0.1mol/L的四氢硼钠水溶液,滴加完毕后,采用30%的氨水调节溶液PH值至13,反应3h,反应完成后,将反应后的溶液冷却至40℃,加入含5%的SiO2改性的明胶(1%)水溶液,搅拌2h后停止反应,高速离心分离,去除上层溶液,沉淀物用50mL去离子水分散后即得水基量子点除醛添加剂;其中,改性明胶的制备方法为:将5%的载体溶液分散于1%的明胶中,并加入羟丙基甲基纤维素或海藻酸钠为保护剂、十六烷基三甲基溴化铵、十二烷基苯磺酸钠作为稳定剂,加热后即得。
实施例4
一种水基量子点除醛功能添加剂的制备方法,包括以下步骤:
向含有2%明胶的0.3mol/L的碳酸钴溶液中通入氮气,130r/min下搅拌,升温至50℃后,滴加4g/L的盐酸多巴胺及0.03mol/L的四氢硼钠水溶液,滴加完毕后,采用30%的氨水调节溶液PH值至12,反应3h,反应完成后,将反应后的溶液冷却至30℃,加入含5%的SiO2改性的明胶(1%)水溶液,搅拌2h后停止反应,高速离心分离,去除上层溶液,沉淀物用50mL去离子水分散后即得水基量子点除醛添加剂;其中,改性明胶的制备方法为:将5%的载体溶液分散于1%的明胶中,并加入羟丙基甲基纤维素或海藻酸钠为保护剂、十六烷基三甲基溴化铵、十二烷基苯磺酸钠作为稳定剂,加热后即得。
实施例5
一种水基量子点除醛功能添加剂的制备方法,包括以下步骤:
向含有2%明胶的0.1-0.5mol/L的硫酸铂溶液中通入氮气,140r/min下搅拌,升温至50℃后,滴加4g/L的盐酸多巴胺及0.07mol/L的四氢硼钠水溶液,滴加完毕后,采用30%的氨水调节溶液PH值至11,反应3h,反应完成后,将反应后的溶液冷却至35℃,加入含5%的SiO2改性的明胶(1%)水溶液,搅拌2h后停止反应,高速离心分离,去除上层溶液,沉淀物用50mL去离子水分散后即得水基量子点除醛添加剂;其中,改性明胶的制备方法为:将5%的载体溶液分散于1%的明胶中,并加入羟丙基甲基纤维素或海藻酸钠为保护剂、十六烷基三甲基溴化铵、十二烷基苯磺酸钠作为稳定剂,加热后即得。
实施例6
一种水基量子点除醛功能添加剂的制备方法,包括以下步骤:
向含有2.5%明胶的0.4mol/L的硫酸铁溶液中通入氮气,140r/min下搅拌,升温至50℃后,滴加4g/L的盐酸多巴胺及0.02mol/L的四氢硼钠水溶液,滴加完毕后,采用30%的氨水调节溶液PH值至12,反应3h,反应完成后,将反应后的溶液冷却至30℃,加入含5%的SiO2改性的明胶(1%)水溶液,搅拌2h后停止反应,高速离心分离,去除上层溶液,沉淀物用50mL去离子水分散后即得水基量子点除醛添加剂;其中,改性明胶的制备方法为:将5%的载体溶液分散于1%的明胶中,并加入羟丙基甲基纤维素或海藻酸钠为保护剂、十六烷基三甲基溴化铵、十二烷基苯磺酸钠作为稳定剂,加热后即得。
对比例1
本对比例与实施例1的区别在于:S1中不含盐酸多巴胺。
对比例2
本对比例与实施例1的区别在于:S2中明胶未改性。
实验例1
对实施例1-6制得的除醛功能添加剂,以及对比例1-2制得的除醛功能添加剂,采用同样的常规方法混合加入到水性除醛喷剂中后,将所得的水性除醛喷剂试验样品1-8,分别喷在具有同样浓度(初始浓度为0.50mg/m3)的甲醛测试空间内,分别进行性能测试:
需要说明的是,其检测标准依据:《居室空气中甲醛的卫生标准》规定:居室空气中甲醛的最高容许浓度为0.08mg/m3。
表1试验样品1-8的除醛喷剂的除醛性能测试
由表1数据可知,本发明实施例得到除醛功能添加剂加入到水性除醛喷剂中后,所得的水性除醛喷剂的除甲醛性能均优于对比例,且均优于《居室空气中甲醛的卫生标准》规定的标准。
而对比例1中不含盐酸多巴胺,从而使得纳米量子点金属颗粒不易团聚,这样在用于除醛喷剂中后难以聚集,对比例2中明胶未改性,这样在添加到除醛喷剂、乳胶漆等中后分散的不够均匀,从而使得最终的除甲醛的效果均不理想。
以上仅为本发明的优选实施例而已,并不用于限制本发明,对于本领域的技术人员来说,本发明可以有各种更改和变化。凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。
Claims (7)
1.一种水基量子点除醛功能添加剂的制备方法,其特征在于,包括以下步骤:
S1.向含有明胶的量子点金属盐溶液中通入氮气,搅拌、升温后,滴加盐酸多巴胺及四氢硼钠水溶液,滴加完毕后,调节溶液PH值至11-13,反应一段时间;所述量子点金属盐包括Ni、Co、Fe、Ag、Mn、Zn、Pt、Au的硫酸盐、碳酸盐、硝酸盐、氯化盐中的一种或几种;
S2.将反应后的溶液冷却后,加入改性明胶水溶液,搅拌后,高速离心分离,去除上层溶液,沉淀物经分散后即得水基量子点除醛添加剂;
其中,所述改性明胶包括明胶和载体,所述载体包括SiO2、CaCO3、TiO2、蒙脱土或滑石粉中的一种或几种;所述改性明胶的制备方法为:将5%的载体溶液分散于1%的明胶中,并加入羟丙基甲基纤维素或海藻酸钠为保护剂、十六烷基三甲基溴化铵、十二烷基苯磺酸钠作为稳定剂,加热后即得。
2.根据权利要求1所述水基量子点除醛功能添加剂的制备方法,其特征在于,S1中,所述含有明胶的量子点金属盐溶液为含有1-3%明胶的0.1-0.5mol/L的量子点金属盐溶液。
3.根据权利要求1所述水基量子点除醛功能添加剂的制备方法,其特征在于,S1中,搅拌速率为100-150 r/min,升温至30-60℃。
4.根据权利要求1所述水基量子点除醛功能添加剂的制备方法,其特征在于,S1中,所述盐酸多巴胺的浓度为1-5g/L,四氢硼钠水溶液的浓度为0.01-0.1mol/L。
5.根据权利要求1所述水基量子点除醛功能添加剂的制备方法,其特征在于,S1中采用30%的氨水调节溶液PH。
6.根据权利要求1所述水基量子点除醛功能添加剂的制备方法,其特征在于,所述S2中冷却至20-40℃。
7.一种量子点除醛功能添加剂,其特征在于,由权利要求1-6任一项所述的水基量子点除醛功能添加剂的制备方法制得。
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