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Correction for ‘Synthesis and characterization of AFe2O4 (A: Ni, Co, Mg)–silica nanocomposites and their application for the removal of dibenzothiophene (DBT) by an adsorption process: kinetics, isotherms and experimental design’ by Fahimeh Vafaee et al., RSC Adv., 2021, 11, 22661–22676, https://doi.org/10.1039/D1RA02780H.

The authors regret an error in Fig. 4 where a section of the XRD for 4(a) and (b) is identical.Open in a separate windowFig. 4(a) The XRD pattern of sample 3 after adsorption of DBT. (b) The XRD pattern of sample 3 before adsorption of DBT.The authors have repeated the experiment and provided new data for Fig. 4. An independent expert has viewed the new data and has concluded that it is consistent with the discussions and conclusions presented. The correct Fig. 4 is shown below:The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.  相似文献   

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Correction for ‘Synthesis of a well-dispersed CaFe2O4/g-C3N4/CNT composite towards the degradation of toxic water pollutants under visible light’ by Fei Liu et al., RSC Adv., 2019, 9, 25750–25761.

The authors regret that mistakes were made during the preparation of Fig. 1 in the published article. In the original article, Fig. 1 presented XRD data for CaFe2O4/CNT, which inadvertently duplicated the data for CaFe2O4. In addition, the spectra in the original figure do not match with the relevant discussion of Fig. 1 (on page 25753–25754) which referred to XRD patterns for g-C3N4, CaFe2O4 and CaFe2O4/g-C3N4/CNT composite. The correct image for Fig. 1 is shown below but no changes are required to the associated discussion of Fig. 1.Open in a separate windowFig. 1XRD patterns of the as-prepared CaFe2O4 and CaFe2O4/g-C3N4/CNT composite.The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.  相似文献   

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Correction for ‘Green-synthesised cerium oxide nanostructures (CeO2-NS) show excellent biocompatibility for phyto-cultures as compared to silver nanostructures (Ag-NS)’ by Qaisar Maqbool, RSC Adv., 2017, 7, 56575–56585, https://doi.org/10.1039/c7ra12082f.

The author regrets that Fig. 4 and and55 of the original article did not appropriately represent the findings.Open in a separate windowFig. 4Comparative TGA analysis of CeO2-NS and Ag-NS.Open in a separate windowFig. 5FTIR spectrum of CeO2-NS and Ag-NS.The correct version of Fig. 4 is shown below. In addition, the associated text on page 56578 “Experimental findings show total mass loss…” should be changed to “Experimental findings show total mass loss of 57.53% by CeO2-NS and 61.12% by Ag-NS.” Fig. 5 of the original article shows only the plot of selected data points. In order to provide clarity to readers, it should be replaced with the following original FTIR plots (complete scan).The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.  相似文献   

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Correction for ‘Efficient removal of cobalt from aqueous solution using β-cyclodextrin modified graphene oxide’ by Wencheng Song et al., RSC Adv., 2013, 3, 9514–9521.

The authors regret that Fig. 1 and and33 were incorrect in the original article. The SEM images of both GO and β-CD, and the Raman spectra of both, were confused with other samples. The correct versions of Fig. 1 and and33 are presented below.Open in a separate windowFig. 1SEM images of (a) GO and (b) β-CD-GO.Open in a separate windowFig. 2Raman spectra of GO and β-CD-GO.The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.  相似文献   

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Correction for ‘A novel biocompatible, simvastatin-loaded, bone-targeting lipid nanocarrier for treating osteoporosis more effectively’ by Shan Tao et al., RSC Adv., 2020, 10, 20445–20459, DOI: 10.1039/D0RA00685H.

The authors regret that incorrect versions of Fig. 7, ,99 and and1010 were included in the original article. The correct versions of Fig. 7, ,99 and and1010 are presented below.Open in a separate windowFig. 7Histological analysis of organs from all experimental groups. H&E staining of heart, liver, spleen, lung, kidney, indicating the carrier has good biocompatibility. Scale bar = 50 μm.Open in a separate windowFig. 9Alkaline phosphatase (ALP) activity (arrows) and tartrate-resistant acid phosphatase (TRAP) assay results (arrowheads) of bone tissue sections. Scale bar = 50 μm. The ALP activity is much more high in SIM/LNPs and SIM/ASP6-LNPs groups, while the TRAP activity is the opposite.Open in a separate windowFig. 10Histological assessment of bone formation in all experimental groups. (A) HE staining of femur bone. Scale bar = 50 μm. Histology of bone in the all experimental groups shows all ovariectomized groups had a higher amount of adipose tissue than Sham group. The trabecular bone is much more prominent in SIM/LNPs and SIM/ASP6-LNPs groups. (B) Immunohistochemical staining for BMP-2 in typical newly-formed bone tissue (red arrows) and immunohistochemical staining for the osteogenic markers osteopontin (OPN, arrows) and osteocalcin (OCN, arrowheads). Scale bar = 50 μm. The BMP-2, OPN, OCN are much more prominent in SIM/LNPs and SIM/ASP6-LNPs groups.The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.  相似文献   

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Correction for ‘Improving the inhibitory effect of CXCR4 peptide antagonist in tumor metastasis with an acetylated PAMAM dendrimer’ by Changliang Liu et al., RSC Adv., 2018, 8, 39948–39956.

The authors regret that the term “CXCL12” was incorrectly displayed as “CXCR12” in Scheme 1 and Fig. 6(a)–(c) in the original article. The correct versions of Scheme 1 and Fig. 6(a)–(c) are presented below.Open in a separate windowScheme 1Schematic illustration of the preparation of the PAC80–E5 complex and the process of anti-tumor metastasis of the E5 peptide in the presence of PAC80.Open in a separate windowFig. 6(a–c) The inhibitory effect of E5 and PAC80–E5 on: (a) MCF-7; (b) MDA-MB-231; and (c) 4T1 cells detected by transwell assay. The CXCL12 supplemented sample without E5 or PAC80–E5 was set as 100% as the control. Error bars represent the standard deviation (n = 3).The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.  相似文献   

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Correction for ‘Nano- and micro-structural control of WO3 photoelectrode films through aqueous synthesis of WO3·H2O and (NH4)0.33WO3 precursors’ by Hiroaki Uchiyama et al., RSC Adv., 2020, 10, 11444–11449.

The Royal Society of Chemistry regrets that an incorrect version of Fig. 6 was included in the original article. The correct version of Fig. 6 is presented below.Open in a separate windowFig. 6Cross-section SEM images of the WO3 heat-treated films obtained from WO3·H2O (a) and (NH4)0.33WO3 (b) precursor layers on silica glass substrates.The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.  相似文献   

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Correction for ‘Helium-induced damage in U3Si5 by first-principles studies’ by Yibo Wang et al., RSC Adv., 2021, 11, 26920–26927. DOI: 10.1039/D1RA04031F.

The authors regret that an incorrect version of Fig. 4 was included in the original article. The correct version of Fig. 4 is presented below.Open in a separate windowFig. 4The dependence of the trapping energy on the number of He atoms trapped in Vac-U, Vac-Si1, and Vac-Si2 vacancies of U3Si5.The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.  相似文献   

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Correction for ‘A guanidyl-functionalized TiO2 nanoparticle-anchored graphene nanohybrid for enhanced capture of phosphopeptides’ by Hailong Liu et al., RSC Adv., 2018, 8, 29476–29481.

The authors regret that there was an error in Fig. 3 of the original article, as the three parts of the figure were labelled incorrectly. The correct version of Fig. 3 is presented below.Open in a separate windowFig. 1MALDI-TOF mass spectra of tryptic digests of β-casein: (a) direct analysis and after enriched by (b) GF-TiO2–GO and (c) TiO2 (# dephosphorylated fragment).The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.  相似文献   

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Correction for ‘An indenocarbazole-based host material for solution processable green phosphorescent organic light emitting diodes’ by Eun Young Park et al., RSC Adv., 2021, 11, 29115–29123. DOI: 10.1039/D1RA04855D.

The authors regret that an incorrect version of Fig. 1 was included in the original article. The correct version of Fig. 1 is presented below.Open in a separate windowFig. 1HOMO, LUMO distributions and energy level of PCIC predicted through DFT and TD-DFT calculations.The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.  相似文献   

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Correction for ‘A p-type multi-wall carbon nanotube/Te nanorod composite with enhanced thermoelectric performance’ by Dabin Park et al., RSC Adv., 2018, 8, 8739–8746.

The authors regret that an incorrect version of Fig. 8 was included in the original article. The correct version of Fig. 8 is presented below.Open in a separate windowFig. 1FE-SEM images of MWCNT/Te nanorod composites with various MWCNT contents (a) 1 wt%, (b) 3 wt%, and (c) 5 wt%.The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.  相似文献   

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Correction for ‘Chrysomycins A–C, antileukemic naphthocoumarins from Streptomyces sporoverrucosus’ by Shreyans K. Jain et al., RSC Adv., 2013, 3, 21046–21053, https://doi.org/10.1039/c3ra42884b.

The authors regret that incorrect versions of Fig. 6 and Fig. 7 were included in the original article. The correct versions of Fig. 6 and and77 are presented below.Open in a separate windowFig. 6Influence of compounds 1–3 on the nuclear morphology of human leukaemia HL-60 cells. The cells were treated with 1, 3 and 5 μM concentrations of these compounds for 24 h and stained with Hoechst 33258 for 40 min. The altered nuclear morphology and apoptotic bodies indicated by white arrows are seen in treated cells while the nuclei of the untreated cells were round and intact.Open in a separate windowFig. 7Phase contrast microscopy of compound-treated leukaemia HL-60 cells. Cells were treated with compounds 1–3 at 1, 3 and 5 μM for 24 h and visualized using a phase contrast microscope (Olympus1X72). The morphology of treated cells altered in a concentration-dependent manner, while the untreated cells remained healthy.The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.  相似文献   

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Fei Jia  Shuyu Lv  Sha Xu 《RSC advances》2019,9(53):30888
Correction for ‘Bio-conjugation of graphene quantum dots for targeting imaging’ by Fei Jia et al., RSC Adv., 2017, 7, 53532–53536.

The authors regret that the versions of Fig. 2 and and44 displayed in the original article were incorrect. The loading dye in Fig. 2c should be the artificial marker for molecular weight analysis. The original Fig. 4 did not support the EGFR binding due to the cell endocytosis, and the result has been revised with an improved data set. The correct versions of Fig. 2 and and44 are shown below.Open in a separate windowFig. 2(a) The sucrose DGU gradient used for purifying the conjugates. (b) The desired SA@GQDs positions in the DGU column. (c) PL image of the DGU column after ultracentrifuge. (d) Bolt 4–12% Bis–Tris gel electrophoresis analysis of SA@GQDs, anti-mouse@GQDs and Erbitux@GQDs, respectively. The loading dye with confirmed molecule weight was tested as references. (e) The cell viability of conjugate Erbitux@GQDs (SCC cell).Open in a separate windowFig. 4(a) SCC cell imaging by Erbitux@GQDs which is binding to the EGFR receptor of SCC cell membrane. (b) The bright field, and PL picture at different channels. After merging the PL picture of Dapi and GFP channels, the successful staining of membrane and nucleus was observed. The quantum yield of GQDs is much lower than Dapi, and we have to tune the contrast/brightness to reach the same quality between Dapi and GQDs. The emission of Dapi also has some signal in GQDs channel, and we have re-draw the data to get rid of the Dapi signal.The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.  相似文献   

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Correction for ‘Non-thermal plasma assisted surface nano-textured carboxymethyl guar gum/chitosan hydrogels for biomedical applications’ by Ganeswar Dalei et al., RSC Adv., 2019, 9, 1705–1716.

The authors regret that incorrect images were mistakenly included in Fig. 7 of the original article, and in the graphical abstract. The correct versions of Fig. 7 and the graphical abstract are presented below. These changes do not affect the overall conclusions of the paper.Open in a separate windowFig. 1SEM images of (a) HG@UT, (b) HG@Ar, (c) HG@O2 and (d) HG@ Ar + O2. The corrected graphical abstract is presented below.The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.  相似文献   

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Li Han  Tao Wang 《RSC advances》2018,8(37):21029
Correction for ‘Preparation of glycerol monostearate from glycerol carbonate and stearic acid’ by Li Han et al., RSC Adv., 2016, 6, 34137–34145.

The authors regret that Fig. 6 in the original article was incorrect. The caption referred to 13C NMR spectra, whereas the figure itself was an expanded version of the 1H NMR shown in Fig. 5. The correct version of Fig. 6 is presented below.Open in a separate windowFig. 6 13C NMR spectra of GMS.The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.  相似文献   

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Correction for ‘Structure evolution, amorphization and nucleation studies of carbon-lean to -rich SiBCN powder blends prepared by mechanical alloying’ by Daxin Li et al., RSC Adv., 2016, 6, 48255–48271.

The authors regret that Fig. 13 was displayed incorrectly in the original article. Due to a data processing error, partially repetitive data was displayed for the entry for 10 h. The correct version of Fig. 13 is shown below.Open in a separate windowFig. 13Solid-state 29Si NMR spectra of carbon-lean C2 (a) and carbon-rich C9 (b) powder blends subjected to different hours of milling.The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.  相似文献   

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