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Graphene oxide is one of the most popular 2D materials available. This is due to the wide range of fields that it can be applied to. It has a distinct advantage over other 2d materials (such as graphene), as it is easily dispersed within solution; allowing for processing at high concentrations. This has opened it up for use in applications such as optical coatings, transparent conductors, thin-film batteries, chemical resistant coatings, water purification, and many more.

Ossila have two types of graphene oxide powders available, with flake sizes between 1-5um and 1-50um. In addition, we also offer pre-dispersed graphene oxide solutions for simple instant use.

Graphene Oxide Powder

Graphene Oxide Powder StructureGraphene Oxide Powder XRD

  • List of products
  • What is graphene oxide?
  • Dispersion guides
  • Technical data and images
  • Publications
  • Related Products

Product List

MSDS Graphene Oxide Powder MSDS

Graphene Oxide Powders

Product codeM880M881M882
Flake Size100 - 200nm1-5 μm1-50 μm
Flake Thickness0.8 - 1.2 nm0.8-1.2 nm0.8-1.2 nm
Single layer ratio>99%>99%>99%
Purity>99%>99%>99%
Amount100mg, 500mg500mg, 1g500mg, 1g
Packaging InformationLight resistant bottleLight resistant bottleLight resistant bottle

MSDS Graphene Oxide Solutions MSDS

Graphene Oxide Solutions

Product codeM883M884M885M886
Flake Sizes1-5 μm1-5 μm1-50 μm1-50 μm
Concentration5 mg.ml-10.5 mg.ml-15 mg.ml-10.5 mg.ml-1
SolventsWater:IPAWater:IPAWater:IPAWater:IPA
Solution Volume100 ml100 ml100 ml100 ml
Packaging Information4 x 25 ml bottles4 x 25 ml bottles4 x 25 ml bottles4 x 25 ml bottles


What Graphene Oxide is

Graphene oxide (GO), also referred to as graphite/graphitic oxide, is obtained by treating graphite with oxidisers, and results in a compound of carbon, oxygen, and hydrogen in variable ratios.

The structure and properties of GO are much dependent on the particular synthesis method and degree of oxidation. With buckled layers and an interlayer spacing almost two times larger (~0.7 nm) than that of graphite,it typically still preserves the layer structure of the parent graphite.

GO absorbs moisture proportionally to humidity and swells in liquid water. GO membranes are vacuum-tight and impermeable to nitrogen and oxygen, but permeable to water vapours. The ability to absorb water by GO depends on the particular synthesis method and also shows a strong temperature dependence.

GO is considered as an electrical insulator for the disruption of its sp2 bonding networks. However, by manipulating the content of oxygen-containing groups through either chemical or physical reduction methods, the electrical and optical properties of GO can be dynamically tuned. To increase the conductivity, oxygen groups are removed by reduction reactions to reinstall the delocalised hexagonal lattice structure. One of the advantages GO has over graphene is that it can be easily dispersed in water and other polar organic solvents. In this way, GO can be dispersed in a solvent and reduced in situ, resulting in potentially monodispersed graphene particles.

Due to its unique structure, GO can be functionalised in many ways for desired applications, such as optoelectronics, drug delivery, chemical sensors, membrane filtration, flexible electronics, solar cells and more.

GO was first synthesised by Brodie (1859), followed by Hummers' Method (1957), and later on by Staudenmaier and Hofmann methods. Graphite (graphene) oxide has also been prepared by using a "bottom-up" synthesis method (Tang-Lau method) where glucose is the sole starting material. The Tang-Lau method is considered to be easier, cheaper, safer and more environmentally-friendly. The thickness, ranging from monolayer to multilayers, can by adjusted using the Tang-Lau process. The effectiveness of an oxidation process is often evaluated by the carbon/oxygen ratios of the GO.


Dispersion Guides

Due to the presence of oxygen and hydroxide groups, the dispersibility of this material is significantly better than other 2d materials (such as graphene). High concentrations of GO can be dispersed in polar solvents, such as water. At Ossila, we have found that the most stable solutions can be produced using the following recipe:

  • Weigh out desired amount of material, this can go up to at least 5 mg.ml-1.
  • Add 1:1 ratio of deionized water to isopropyl alcohol.
  • Shake vigorously to break up material.
  • A short treatment in an ultrasonic bath will rapidly disperse the material.
  • For larger flakes, use a mechanical agitator instead (as sonication may damage the flakes).


Technical Data

General Information

CAS number7782-42-5 (graphite)
Chemical formulaCxHyOz
Recommended SolventsH2O, DMF, IPA
Synonyms
  • Single layer GO
  • GO
Classification / Family2D semiconducting materials, Carbon nanomaterials, Graphene, Organic electronics
ColourBlack/Brown Sheets/Powder

Product Images

Monolayer Graphene OxideGraphene Oxide SEM
SEM Images of flakes on silicon.


Publications

  • An improved Hummers method for eco-friendly synthesis of graphene oxide, J. Chen et al., Carbon 64, 225-229 (2013); http://dx.doi.org/10.1016/j.carbon.2013.07.055.
  • Synthesis of few-layered, high-purity graphene oxide sheets from different graphite sources for biology, D. A. Jasim et al., 2D Mater. 3, 014006 (2016); doi:10.1088/2053-1583/3/1/014006.
  • Preparation and Characterization of Graphene Oxide, J. Song et al., J. Nanomater., 276143 (2014); http://dx.doi.org/10.1155/2014/276143.
  • The chemistry of graphene oxide, D. R. Dreyer et al., Chem. Soc. Rev., 39, 228–240 (2010); DOI: 10.1039/b917103g.
  • Preparation of small-sized graphene oxide sheets and their biological applications, M. Zhang et al., J. Mater. Chem. B, 4, 121 (2016); DOI: 10.1039/c5tb01800e.
  • Graphene Oxide: Preparation, Functionalization, and Electrochemical Applications, D. Chen et al., Chem. Rev., 112, 6027−6053 (2012); dx.doi.org/10.1021/cr300115g.
  • Preparation of Graphitic Oxide, W. Hummer et al., J. Am. Chem. Soc., 80 (6), 1339–1339 (1958); DOI: 10.1021/ja01539a017.
  • Improved Synthesis of Graphene Oxide, D. C. Marcano et al., ACS Nano, 4 (8), 4806–4814 (2010); DOI: 10.1021/nn1006368.
  • Fast and fully-scalable synthesis of reduced graphene oxide, S. Abdolhosseinzadeh et al., Sci. Rep., 5:10160 (2015); DOI: 10.1038/srep10160.


To the best of our knowledge, the technical information provided here is accurate. However, Ossila assume no liability for the accuracy of this information. The values provided here are typical at the time of manufacture and may vary over time and from batch to batch.

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  巴比妥钠缓冲液主要是由巴比妥、巴比妥钠、氯化钠等组成,pH值为7.4,常用于血清总补体活性(CH50)测定中制备绵羊红细胞悬液,亦可以用于制备致敏性绵羊红细胞等。  巴比妥钠缓冲液配置操作步骤介绍:  一、绵羊红细胞的制备  1、取绵羊颈静脉血,立即加入等量的抗凝剂,充分混匀。  2、加入适量的1×巴比妥缓冲液,离心,弃上清。  3、重复(步骤2)2次,以便清洗干净。  4、取2ml上述绵羊红细胞溶液,加入98ml 1&... 查看更多>
我们可以通过运用体外细胞培养技术,在淡水软体动物门锥实螺属的培养细胞上,重新构建发动基本呼吸行为的 S 细胞网络. 这种体外重建的网络能够产生节律性运动形式并与整体所见的运动形式相似。因此,这种体外细胞培养方法,使得我们能够进行有关节律性活动神经元基础的基本研究,而这种研究在整体动物或不完整的动物身上都是难以实现的。 查看更多>
上海拓旸生物科技有限公司在发布的硼酸-硼砂缓冲液(pH7.4-9.0)供应信息,浏览与硼酸-硼砂缓冲液(pH7.4-9.0)相关的产品或在搜索更多与硼酸-硼砂缓冲液(pH7.4-9.0)相关的内容。 查看更多>
规格(核心参数):PH11.001L/瓶 查看更多>
当往某些溶液中加入一定量的酸和碱时,有阻碍溶液pH变化的作用,称为缓冲作用,这样的溶液叫做缓冲溶液。弱酸及其盐的混合溶液(如HOAc与NaOAc),弱碱及其盐的混合溶液(如NH3·H2O与NH4Cl)等都是缓冲溶液。... 查看更多>
袋装pH标准缓冲液(粉剂)是由上海创萌生物科技有限公司代理或销售的lc品牌的试剂,产品来源于上海。上海创萌生物科技有限公司是中国最权威的袋装pH标准缓冲液(粉剂)试剂销售服务商之一,在上海等地方销售袋装pH标准缓冲液(粉剂)试剂已经多年。生物在线为您提供众多企业袋装pH标准缓冲液(粉剂)仪器产品及图片,以便挑选到性价比高,合适的袋装pH标准缓冲液(粉剂)产品 查看更多>
改良磷酸盐缓冲液(Modified Phosphate Buffer)用 途:用于小肠结肠炎耶尔森氏菌的增菌培养。(GB4789.8-2008)原 理:山梨醇提供碳氮源,磷酸氢二钠和磷酸二氢钠为缓冲液,胆盐抑制革兰氏阳性菌,氯化钠提供细胞所需要的渗透压。配方(L):磷酸氢二钠 8.23g... 查看更多>
蛋白上样缓冲液(SDS-PAGE loading buffer)是一种经过改良的以溴酚蓝为染料,5倍浓缩的SDS-PAGE凝胶电泳上样缓冲液,用于常规的SDS-PAGE蛋白电泳样品上样。储存条件:20℃保存,一年有效。 查看更多>
Montana Molecular公司简介/产品代理进口采购 查看更多>
分子生物学实验中常用的电泳缓冲液主要有三种:TAE、TBE 和 TPE.TBE 与 TPE 缓冲容量高,DNA 分离效果好,但 TPE 会导致 DNA 片段回收时含磷酸盐浓度高,容易使 DNA 沉淀。TAE 缓冲容量低,但价格较便宜,TBE 缓冲液含有的 EDTA  可螯合二价阳离子,可抑制 DNase 活性,防止 PCR 扩增产物降解。TAE 缓冲液的特点:TAE 是使用最广泛的缓冲系统。其特点是超螺旋在其中电泳时更符合实际相对分... 查看更多>
南京森贝伽生物科技有限公司在发布的GTBE电泳缓冲液供应信息,浏览与GTBE电泳缓冲液相关的产品或在搜索更多与GTBE电泳缓冲液相关的内容。 查看更多>
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配制缓冲溶液常用方法有:
1、根据所需求的酸碱性选择合适的缓冲对,若是配制酸性缓冲液就选择弱酸与弱酸盐缓冲对;若是配制碱性缓冲液就选择弱碱与弱碱盐缓冲对。
2、根据所需要控制的PH范围以及弱酸和弱碱的解离常数(pKa/pKb)选择具体的共轭酸碱对,公式为PH=pKa±1=(14-pKb)±1。
3、根据公式计算缓冲溶液的组分比,酸性缓冲液PH=pKa-lgc酸/c盐,碱性缓冲液PH=14-pKb+lgc碱/c盐。
4、根据共轭酸碱对以及其组分比配制缓冲液,方法同普通溶液。
举例:试配制一种缓冲液,体积为1L,PH能维持在10.25左右。
a、依题意选择弱碱与弱碱盐的共轭对;
b、由PH=(14-pKb)±1,算出pKb在3.75与4.75之间,查弱碱的解离常数表可知氨水(pKb=4.75)符合要求,故可选择NH3-NH4Cl体系;
c、由PH=14-pKb+lgc碱/c盐,算出c(氨水)/c(氯化铵)=10;
d、设氨水的浓度为10mol/L,则氯化铵的浓度为1mol/L,所以在浓度为10mol/L体积为1L的氨水中加入1mol的氯化铵即可。
PH在4-7之间常见缓冲液有哪些?
缓冲液的pH值与该酸的电离平衡常数K及盐和酸的浓度有关.酸和盐浓度相等时,溶液的pH值与PK值相同.酸和盐浓度等比例增减时,溶液的pH值不变.酸和盐浓度相等时,缓冲液的缓冲效率为最高.
缓冲液是一种能在加入少量酸或碱时抵抗pH改变的溶液。
缓冲溶液的缓冲能力(用缓冲容量表示)与总浓度和组分比有关.总浓度越大,缓冲容量越大;当总浓度一定时,缓冲组分的浓度比越接近1:1,缓冲容量越大。由弱酸及其盐、弱碱及其盐组成的混合溶液,能在一定程度上抵消、减轻外加强酸或强碱对溶液酸碱度的影响,从而保持溶液的pH值相对稳定。这种溶液称为缓冲溶液。
酶要在一定的活性中才有活性,强酸强碱都可以使其失去活性,故需要加入缓冲液,使在一定的Ph值中,保持酶的活性。

酶提取技术,属地球化学勘查学科。其是由克拉克(J.R.Clark)等人于20世纪80年代末和90年代初研制出的一种利用葡萄糖氧化酶提取矿物颗粒表面的非晶质锰的氧化膜寻找隐伏矿的方法。1995年以后已广泛应用。
我现在遇到一个题目,如题,硼砂是可也用来配置 缓冲溶液,问题是 ,他要我说原因,很纠结~求解啊!!!
缓冲溶液是指在一定范围内,能够使溶液ph不变或变化不大的溶液。
根据组成不同,可分为两种,弱酸及其对应的强碱弱酸盐,弱碱及其对应的强酸弱碱盐。
因为HF可以和NaOH反应生成NaF和水,当NaOH反应完之后,NaF就可以与HF组成缓冲溶液,所以说可以直接使用NaOH和HF来配制缓冲溶液。
这也是一般配制缓冲溶液的方法,也就是用强碱和弱酸(或者强酸和弱碱)来配制缓冲溶液。
缓冲溶液的选择和应用123
3717136502021-07-26
缓冲液如何选择?
缓冲溶液的配置方法 123
xiaoliu062018-01-24
20mmol/L的巴比妥钠(Barbital-Na2,pH8.3,0~4℃)缓冲液,这是要求,谢谢
缓冲液是一种能在加入少量酸或碱和水时抵抗pH改变的溶液.PH缓冲系统对维持生物的正常pH值,正常生理环境起重要作用.多数细胞仅能在很窄的pH范围内进行活动,而且需要有缓冲体系来抵抗在代谢过程中出现的pH变化.在生物体中有三种主要的pH缓冲体系,它们时蛋白质、重碳酸盐缓冲体系.每种缓冲体系所占的分量在各类细胞和器官中是不同的.
当往某些溶液中加入一定量的酸和碱时,有阻碍溶液pH变化的作用,称为缓冲作用,这样的溶液叫做缓冲溶液。