Erratum to: Colloid Polym Sci
DOI 10.1007/s00396-014-3309-6
The original version of this article, unfortunately, contained an error. The acronyms for N-isopropyl acrylamide and Poly(N-isopropyl acrylamide) were incorrect. The correct ones are as follows:
N-isopropyl acrylamide (NIPAM)
Poly(N-isopropyl acrylamide) (PNIPAM)
Page No. Column No. Line No. | Incorrect | Correct |
---|---|---|
Page 2 Column 1 Line 20 | poly(N-isopropylacrylamide) (NIPAM) is one of the most | poly(N-isopropylacrylamide) (PNIPAM) is one of the most |
Page 2 Column 1 Line 26 | above the LCST, NIPAM hydrogels become hydrophobic, | above the LCST, PNIPAM hydrogels become hydrophobic, |
Page 2 Column 1 Line 31 | encapsulated in hydrogels based on NIPAM [31]. | encapsulated in hydrogels based on PNIPAM [31]. |
Page 2 Column 1 Line 32 | However, the use of NIPAM-based hydrogels shows | However, the use of PNIPAM-based hydrogels shows |
Page 2 Column 1 Line 35 | erties of NIPAM [2]. The obvious limitation of the | erties of PNIPAM [2]. The obvious limitation of the |
Page 2 Column 1 Line 36 | NIPAM hydrogel is its poor mechanical property in a | PNIPAM hydrogel is its poor mechanical property in a |
Page 2 Column 1 Line 39 | Copolymerisation of NIPAM with water insoluble or | Copolymerisation of N-isopropyl acrylamide (NIPAM) with water insoluble or |
Page 2 Column 2 Line 1 | hydrophilic outer shell of NIPAM and a favourable size | hydrophilic outer shell of PNIPAM and a favourable size |
Page 2 Column 2 Line 8 | shells possess a hydrophilic outer shell of NIPAM and | shells possess a hydrophilic outer shell of PNIPAM and |
Page 2 Column 2 Line 24 | poly(NIPAM-co-MMA) core and NIPAM shell | poly(NIPAM-co-MMA) core and PNIPAM shell |
Table 1 Page 3 | WPNIPAM | WNIPAM |
Page 3 Column 2 Subheading | Preparation of P(NIPAM-co-MMA) core and NIPAM shell microspheres | Preparation of P(NIPAM-co-MMA) core and PNIPAM shell microspheres |
Page 4 Column 1 Line 5 | NIPAM was allowed to be formed similarly as men | PNIPAM was allowed to be formed similarly as men |
Page 5 Column 1 Line 3 | (4, 6, 12 and 24 h), P(NIPAM-co-MMA) core with NIPAM | (4, 6, 12 and 24 h), P(NIPAM-co-MMA) core with PNIPAM |
Page 8 Column 1 Line 21 | core particles, P(NIPAM-co-MMA) core with NIPAM shell | core particles, P(NIPAM-co-MMA) core with PNIPAM shell |
Page 8 Column 1 Line 23 | NIPAM shell particles (Fig. 1). In the synthesis of core parti | PNIPAM shell particles (Fig. 1). In the synthesis of core parti |
Page 8 Column 1 Line 33 | isation were used as seed particles to fabricate NIPAM shell | isation were used as seed particles to fabricate PNIPAM shell |
Page 9 Captions for Fig. 5 a and b | Fig. 5 a SEM micrographs of the core–shell microspheres and oil-loaded core–shell microspheres prepared with different PNIPAM dosages in shell fabrication: i 0 g, ii 0.5 g, iii 1.0 g, iv 1.5 g, v 2.5 g, vi PNIPAM at1.0 g, oil 2 g, vii PNIPAM at 1.0 g, oil 3.5 g viii, and PNIPAM at 1.0 g, oil 5 g. b DLS-based particle size distribution curves of the core–shell microspheres prepared with different PNIPAM dosages in shell fabrication: i 0.5 g, ii 1.0 g, iii 1.5 g and iv 2.5 g | Fig. 5 a SEM micrographs of the core–shell microspheres and oil-loaded core–shell microspheres prepared with different NIPAM dosages in shell fabrication: i 0 g, ii 0.5 g, iii 1.0 g, iv 1.5 g, v 2.5 g, vi NIPAM 1.0 g, oil 2 g, vii NIPAM 1.0 g, oil 3.5 g viii, and NIPAM 1.0 g, oil 5 g. b DLS-based particle size distribution curves of the core–shell microspheres prepared with different NIPAM dosages in shell fabrication: i 0.5 g, ii 1.0 g, iii 1.5 g and iv 2.5 g |
Page 10 Table 2 | WPNIPAM | WNIPAM |
Page 10 Column 2 Line 8 | which was attributed to the stretching NIPAM chains in aque- | which was attributed to the stretching PNIPAM chains in aque- |
Page 10 Column 2 Line 9 | ous solution at 25 °C and the shrinking NIPAM chains on | ous solution at 25 °C and the shrinking PNIPAM chains on |
Page 10 Column 2 Line 13 | NIPAM nanocapsules with temperature-tunable diameter and | PNIPAM nanocapsules with temperature-tunable diameter and |
Page 11 Caption for Fig. 6 | PNIPAM dosages | NIPAM dosages |
Page 11 Column 1 Line 2 | core NIPAM shell microspheres was characterised by DLS | core PNIPAM shell microspheres was characterised by DLS |
Page 11 Column 2 Line 9 | temperatures below the LCST of NIPAM in water, the | temperatures below the LCST of PNIPAM in water, the |
Page 12 Column 1 Line 4 | broken and NIPAM underwent a coil-to-globule transition | broken and PNIPAM underwent a coil-to-globule transition |
Page 12 Column 1 Line 15 | NIPAM Tt (or LCST) of as illustrated in Table 3. Generally, in | PNIPAM Tt (or LCST) of as illustrated in Table 3. Generally, in |
Page 12 Column 1 Line 22 | of pure NIPAM irrespective of incorporation of PMMA. It is | of pure PNIPAM irrespective of incorporation of PMMA. It is |
Page 12 Column 1 Line 25 | surface of which was encircled by NIPAM shell layer that | surface of which was encircled by PNIPAM shell layer that |
Page 12 Column 2 Line 4 | group in NIPAM segment and bending frequency of amide | group in PNIPAM segment and bending frequency of amide |
Page 12 Column 2 Line 8 | the NIPAM segments in all the copolymer spectra, which was | the PNIPAM segments in all the copolymer spectra, which was |
Page 12 Column 2 Line 10 | ison to the NIPAM segments in the core microspheres. | ison to the PNIPAM segments in the core microspheres. |
Page 12 Column 2 Line 12 | due to NIPAM segments which were prominent initially | due to PNIPAM segments which were prominent initially |
Page 13 Column 1 Line 11 | higher NIPAM amount (Fig. 8b(ii)) in comparison to that in | higher PNIPAM amount (Fig. 8b(ii)) in comparison to that in |
Page 13 Column 1 Line 13 | spheres with lesser amount of NIPAM (Fig. 8b(i)). Whereas | spheres with lesser amount of PNIPAM (Fig. 8b(i)). Whereas |
Page 13 Column 1 Line 14 | the peaks due to NIPAM segments at 1,651 and 1,543 cm−1 | the peaks due to PNIPAM segments at 1,651 and 1,543 cm−1 |
Page 13 Column 1 Line 17 | component was only NIPAM that encircled the inner hydro | component was only PNIPAM that encircled the inner hydro |
Page 13 Caption for Fig. 8 b | PNIPAM | NIPAM |
Page 14 Column 1 Line 39 | hydrated NIPAM shells stabilised the loaded olive oil in the | hydrated PNIPAM shells stabilised the loaded olive oil in the |
Page 14 Column 2 Line 17 | increased to 40 °C. The NIPAM shell became hydrophobic | increased to 40 °C. The PNIPAM shell became hydrophobic |
Page 14 Column 2 Line 21 | P( N I PAM-co-MMA) c o r e and NIPAM s h e l l | P( N I PAM-co-MMA) c o r e and PNIPAM s h e l l |
Column 1 is for Left Column
Column 2 is for Right Column
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The online version of the original article can be found at http://dx.doi.org/10.1007/s00396-014-3309-6.
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Devi, N., Kakati, D.K. Erratum to: Thermoresponsive submicron-sized core–shell hydrogel particles with encapsulated olive oil. Colloid Polym Sci 292, 2597–2598 (2014). https://doi.org/10.1007/s00396-014-3381-y
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DOI: https://doi.org/10.1007/s00396-014-3381-y