Nanoparticles are commonly used to avoid the opaque white color of TiO2 based sunscreen. However, a dispersing agent is typically required because of the tendency of the nanoparticles (NPs) to agglomerate. Stearic acid is one kind of dispersing agent often used for sunscreen products. However, according to the MSDS data sheet on stearic acid, stearic acid is highly hazardous to aquatic life and causes irritation on human skin. To avoid this problem, in this study a safer organic dispersing agent extracted from Korean seaweed has been studied to disperse TiO2 nanoparticles, and further use as an active agent in sunscreen products. The presence of phytochemicals in seaweed extract, especially alginate, can disperse TiO2 nanoparticles and improve TiO2 dispersion properties. Results show that seaweed extract can improve the dispersion properties of TiO2 nanoparticles and sunscreen products. Reducing the agglomeration of TiO2 nanoparticles improves sunscreen properties, by making it less opaque white in color, and increasing UV protection value. It was also confirmed that adding seaweed extract into sunscreen products had no irritating effects on the human skin, making it more desirable for cosmetics application.

An optical fluorescence quenching sensor based on functionally modified iron-doped carbon nanoparticles was designed for the selective and sensitive Cr(VI) ion detection. Multifunctional iron-doped carbon nanoparticles were enclosed in the scaffolds of a promising stable nanocarrier system called hyperbranched polyglycerol (HPG), which has been fluorescently modified with 1-pyrene butyric acid using the Steglich esterification procedure. The therapeutic and diagnostic capabilities were boosted when these nanoparticles were enclosed in the fluorescently modified dendritic structure, HPG. Iron-doped carbon nanoparticles coupled with fluorescently modified hyperbranched polyglycerol can be used as a sensor for metal ions and can then be used to successfully remove them from a sample. Moreover, the synthesised nanoparticles demonstrated promising antimicrobial efficacy against bacteria and fungi. These results are also discussed in detail.

As a promising anode for sodium-ion batteries (SIBs), cobalt sulfide ( CoS2) has attracted extensive attention due to its high theoretical capacity, easy preparation, and superior electrochemical activity. However, its intrinsic low conductivity and large volume expansion result in poor cycling ability. Herein, nitrogen-doped carbon-coated CoS2 nanoparticles (N–C@ CoS2) were prepared by a C3N4 soft-template-assisted method. Carbon coating improves the conductivity and prevents the aggregation of CoS2 nanoparticles. In addition, the C3N4 template provides a porous graphene-like structure as a conductive framework, affording a fast and constant transport path for electrons and void space for buffering the volume change of CoS2 nanoparticles. Benefitting from the superiorities, the Na-storage properties of the N–C@CoS2 electrode are remarkably boosted. The advanced anode delivers a long-term capacity of 376.27 mAh g− 1 at 0.1 A g− 1 after 500 cycles. This method can also apply to preparing other metal sulfide materials for SIBs and provides the relevant experimental basis for the further development of energy storage materials.

Decabromodiphenyl ether (BDE209) is a persistent aromatic compound widely associated with environmental pollutants. Given its persistence and possible bioaccumulation, exploring a feasible technique to eradicate BDE209 efficiently is critical for today’s environmentally sustainable societies. Herein, an advanced nanocomposite is elaborately constructed, in which a large number of titanium dioxide ( TiO2) nanoparticles are anchored uniformly on two-dimensional graphene oxide (GO) nanosheets ( TiO2/GO) via a modified Hummer’s method and subsequent solvothermal treatment to achieve efficient photocatalytic degradation BDE209. The obtained TiO2/ GO photocatalyst has excellent photocatalytic due to the intense coupling between conductive GO nanosheets and TiO2 nanoparticles. Under the optimal photocatalytic degradation test conditions, the degradation efficiency of BDE209 is more than 90%. In addition, this study also provides an efficient route for designing highly active catalytic materials.

In this study, gold nanoparticles (AuNPs) were synthesised using green chemistry to decorate multi-walled carbon nanotubes (MWCNTs) made from walnut shells transmission electron microscopy, field-emission scanning electron microscopy (FESEM), atomic force microscopy and fourier transforms infrared spectroscopy were used to diagnose MWCNTs and AuNPs. MWCNT-COOAu, MWCNT-COO and MWCNT-Au were diagnosed by Raman, energy dispersive X-ray analysis and FESEM. The effect of AuNPs, MWCNT-COO, MWCNT-COOAu and MWCNT-Au on pure and serum alkaline phosphatase (ALP) enzyme activity was studied in vitro using the enzyme-substrate 4-nitrophenyl disodium orthophosphate. For pure enzymes, Vmax slightly increased as the concentration of MWCNT-Au, MWCNT-COOAu and MWCNTCOO increased, whereas the Vmax values decreased as the concentration of AuNPs increased. The inhibition type for all NPs varied. For serum ALP enzyme, the Vmax values for Au-based NPs decreased as the concentration of NPs increased. The Vmax values exceeded the standard value at the concentrations of 25, 50 and 75 ppm for MWCNT-Au and MWCNT-COOAu, whereas the Vmax values increased over the standard value for all concentrations of AuNPs.

The ability to both assay the presence of, and to selectively remove ions in a solution is an important tool for waste water treatment in many industrial sectors, especially the nuclear industry. Nuclear waste streams contain high concentrations of heavy metals ions and radionuclides, which are extremely toxic and harmful to the environment, wildlife and humans. For the UK nuclear industry alone, it is estimated that there will be 4.9 million metric tonnes of radioactive waste by 2125, which contains a significant number of toxic radionuclides and heavy metals. This is exacerbated further by increased international growth of nuclear new build and decommissioning. Efforts to remove radionuclides have been focused on the development and optimisation of current separation and sequestering techniques as well as new technologies. Due to the large volumes of waste the techniques must be economical, simple to use and highly efficient in application. Magnetic nanoparticles (MNPs) offer a powerful enhancement of normal ion exchange materials in that they can be navigated to specific places using external magnetic fields and hence can be used to investigate challenges such as, pipework in preparation of decommissioning projects. They also have the potential to be fine-tuned to extract a variety of other radionuclides and toxic heavy metals. It has been demonstrated that with the right functional groups these particles become very strongly selective to radionuclides, such as Uranium. However, this new technology also has the potential to effectively aid nuclear waste remediation at a low cost for the separation of both radionuclides and heavy metals. In this work, we investigate the origin of the selectivity of superparamagnetic iron oxide nanoparticles (SPIONs) to Uranium by making systematic changes to the existing surface chemistry and determining how these changes influence the selectivity. Identifying the mechanism by which selected common nuclear related metals, such as Na(I), K(I), Cs(I), Ca(II), Cu(II), Co(II), Ni(II), Cd(II), Mg(II), Sr(II), Pb(II), Al(III), Mn(II), Eu(III) and Fe(III), are sorbed will allow for specific NP-target (nanoparticle) ion interactions to be revealed. Ultimately this understanding will provide guidance in the design of new targeted NP-ligand constructs for other environmental systems.

A promising approach to enhance catalytic performance of supported heterogeneous nano-metal catalysts is to uniformly disperse active nanoparticles on the support. In this work, N-doped carbon-modified graphene (G@NC) nanosheet is designed and prepared to anchor Pd–Fe bimetallic nanoparticles (Pd–Fe/G@NC). The N-doped carbon modification on graphene surface could construct a sandwich-like structure (G@NC), which not only prevented the re-stacking of graphene nanosheets but also provided confined space for stable anchoring of bimetallic Pd–Fe nanoparticles. Benefitted from the unique structural property and synergetic effect of metal Pd and Fe species, the as-obtained Pd–Fe/G@NC composite displays excellent catalytic activity toward 4-nitrophenol reduction reaction with a turnover frequency of 613.2 min− 1, which is far superior to that of the mono-metal counterparts (Fe/G@NC and Pd/G@NC). More importantly, Pd–Fe/G@NC catalyst also exhibits favorable catalytic performance in the reduction of other nitroaromatic compounds (nitrobenzene, 4-nitrotoluene, 4-chloronitrobenzene, and so on). In addition, Pd–Fe/G@NC can catalyze the oxidation of furfuraldehyde to furoic acid with a high yield of 88.64%. This work provides a new guide for rationally designing and developing advanced supported heterogeneous bimetallic catalyst.