Influence of different β‐nucleating agent on crystallization behavior,morphology, and melting characteristic of multiwalled carbon nanotube‐filled isotactic polypropylene nanocomposites

To obtain isotactic polypropylene (iPP) nanocomposites with high β‐crystal content, TMB5, calcium pimelate and calcium pimelate supported on the surface of nano‐CaCO₃ were used as β‐nucleating agent and MWCNT filled β‐nucleated iPP nanocomposites were prepared. The effect of different β‐nucleating agent and MWCNT on the crystallization behavior and morphology, melting characteristic and β‐crystal content of β‐nucleated iPP nanocomposites were investigated by DSC, XRD and POM. The results indicated that addition of MWCNT increased the crystallization temperature of iPP and MWCNT filled iPP nanocomposites mainly formed α‐crystal. The β‐nucleating agent can induce the formation of β‐crystal in MWCNT filled iPP nanocomposites. The β‐nucleating ability and β‐crystal content in MWCNT filled β‐nucleated iPP nanocomposites decreased with increasing MWCNT content and increased with increasing β‐nucleating agent content due to the nucleation competition between MWCNT and β‐nucleating agents. It is found that the calcium pimelate supported on the surface of inorganic particles as β‐nucleating agent has stronger heterogeneous β‐nucleation than calcium pimelate and TMB5. The MWCNT filled iPP nanocomposites with high β‐crystal content can be obtained by supported β‐nucleating agent. POLYM. COMPOS., 36:635–643, 2015. © 2014 Society of Plastics Engineers     

A novel highly efficient β‐nucleating agent for polypropylene using nano‐CaCO3 as a support

In order to increase the isotactic content of β‐nucleated polypropylene (β‐iPP) and decrease the cost of its production, the investigation and development of novel highly efficient β‐nucleators are important issues. Nano‐CaCO₃ was used as a support to prepare a supported β‐nucleator, nano‐CaCO₃‐supported calcium pimelate. Fourier transform infrared spectral analysis shows that an in situ chemical reaction takes place between nano‐CaCO₃ and pimelic acid. Differential scanning calorimetry results indicate that the crystallization and melting temperatures of β‐phase in supported β‐nucleator‐nucleated iPP are higher than those of calcium pimelate‐nucleated iPP. The β‐nucleating ability of the supported β‐nucleator is little influenced by the cooling rate and crystallization temperature over a wide range. The decreased content of pimelic acid in the supported β‐nucleator slightly decreases the crystallization temperature of iPP but it has no influence on the content of β‐phase in nucleated iPP. A novel supported β‐nucleator has been successfully synthesized via pimelic acid supported on the surface of CaCO₃. The crystallization temperature of iPP and melting temperature of β‐phase in iPP nucleated using the supported β‐nucleator are higher than those of iPP nucleated using calcium pimelate. The concept of a supported nucleator will provide a new way to increase the efficiency of polymer additives and to decrease the amounts of them that need to be used by using nanoparticles as supports. Copyright © 2010 Society of Chemical Industry     

Mechanical and thermal characteristics and morphology of polyamide 6/isotactic polypropylene blends in the presence of a β‐nucleating agent

The mechanical and thermal characteristics and morphology of polyamide 6 (PA6)/isotactic polypropylene (iPP) blends (10/90 w/w) prepared with different processing procedures and incorporated with an aryl amide nucleating agent, a kind of β‐nucleating agent (β‐NA) for iPP, were investigated. The yield strength and flexural modulus of the blends decreased as β‐NA was introduced into the blends, whereas the impact strength and elongation at break improved. The crystalline structures of the blends closely depended on (1) the processing conditions and (2) competition between the β‐nucleating effect of β‐NA and the α‐nucleating effect of PA6 for iPP. Scanning electron microscopy, differential scanning calorimetry, and X‐ray diffraction were adopted to reveal the microstructures of the blends. At a low β‐NA content (<0.1 wt %), the α‐phase iPP dominated the blends, whereas the relative content of the β‐phase iPP increased remarkably when the β‐NA content was not less than 0.1 wt %. The processing conditions also showed profound influences on the supermolecular structures of iPP; this resulted in different mechanical properties of the blends. As for PA6, the crystallization behavior and crystalline structure did not exhibit obvious changes, but PA6 did play an important role in the epitaxial crystallization of iPP on PA6. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

β‐Nucleation of pimelic acid supported on metal oxides in isotactic polypropylene

To investigate the nucleation of metal pimelate for isotactic polypropylene (iPP) crystallization, iPP filled with a series of metal oxides with and without metal pimelate on their surface was prepared. There was a chemical reaction between pimelic acid (PA) and metal oxides MgO, CaO, BaO or ZnO, but not TiO₂. The corresponding metal pimelate formed by the chemical reaction between PA and MgO, CaO, BaO or ZnO had a different influence on the crystallization behavior and melting characteristics of iPP. Addition of metal oxides increased the crystallization temperature of iPP and mainly formed α‐phase due to the heterogeneous α‐nucleation of metal oxides. The α‐nucleation of CaO could be easily changed into β‐nucleation using CaO‐supported PA, and 90.1% β‐phase was obtained. The β‐nucleation of BaO could be markedly enhanced by barium pimelate formed using supported PA. However, no β‐phase was observed for iPP filled with MgO‐ or ZnO‐supported PA. The various metal oxides with supported PA had a different influence on the crystallization behavior and melting characteristics of iPP due to the different structure of metal pimelate formed by chemical reaction between PA and the metal oxides. Copyright © 2012 Society of Chemical Industry     

Nonisothermal crystallization and melting behavior of β‐nucleated isotactic polypropylene and polyamide 66 blends

A highly novel nano‐CaCO₃ supported β‐nucleating agent was employed to prepare β‐nucleated isotactic polypropylene (iPP) blend with polyamide (PA) 66, β‐nucleated iPP/PA66 blend, as well as its compatibilized version with maleic anhydride grafted PP (PP‐g‐MA), maleic anhydride grafted polyethylene‐octene (POE‐g‐MA), and polyethylene‐vinyl acetate (EVA‐g‐MA), respectively. Nonisothermal crystallization behavior and melting characteristics of β‐nucleated iPP and its blends were investigated by differential scanning calorimeter and wide angle X‐ray diffraction. Experimental results indicated that the crystallization temperature (T) of PP shifts to high temperature in the non‐nucleated PP/PA66 blends because of the α‐nucleating effect of PA66. T of PP and the β‐crystal content (K_β) in β‐nucleated iPP/PA66 blends not only depended on the PA66 content, but also on the compatibilizer type. Addition of PP‐g‐MA and POE‐g‐MA into β‐nucleated iPP/PA66 blends increased the β‐crystal content; however, EVA‐g‐MA is not benefit for the formation of β‐crystal in the compatibilized β‐nucleated iPP/PA66 blend. It can be relative to the different interfacial interactions between PP and compatibilizers. The nonisothermal crystallization kinetics of PP in the blends was evaluated by Mo's method. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

A novel β‐nucleating agent for isotactic polypropylene

The nucleating ability of p‐cyclohexylamide carboxybenzene (β‐NA) towards isotactic polypropylene (iPP) was investigated by differential scanning calorimetry, X‐ray diffraction, polarized optical microscopy and scanning electron microscopy. β‐NA is identified to have dual nucleating ability for α‐iPP and β‐iPP under appropriate kinetic conditions. The formation of β‐iPP is dependent on the content of β‐NA. The content of β‐phase can reach as high as 96.96% with the addition of only 0.05 wt% β‐NA. Under non‐isothermal crystallization the content of β‐iPP increases with increasing cooling rate. The maximum β‐crystal content is obtained at a cooling rate of 40 °C min^–1. The supermolecular structure of the β‐iPP is identified as a leaf‐like transcrystalline structure with an ordered lamellae arrangement perpendicular to the special surface of β‐NA. Under isothermal crystallization β‐crystals can be formed in the temperature range 80–140 °C. The content of β‐crystals reaches its maximum value at a crystallization temperature of 130 °C. © 2012 Society of Chemical Industry     

A highly active and selective β‐nucleating agent for isotactic polypropylene and crystallization behavior of β‐nucleated isotactic polypropylene under rapid cooling

Zinc adipate (Adi‐Zn) was observed to be a highly active and selective β‐nucleating agent for isotactic polypropylene (iPP). The effects of Adi‐Zn on the mechanical properties and the β‐crystals content of nucleated iPP were investigated. The impact strength of iPP nucleated with 0.2 wt % Adi‐Zn was 1.8 times higher than that of neat iPP. In addition, wide‐angle X‐ray diffraction analysis indicated that the content of β‐crystals in nucleated iPP (k_β value) reached 0.973 with 0.1 wt % Adi‐Zn, indicating that Adi‐Zn is a highly active and selective β‐nucleating agent for iPP. Furthermore, fast scanning chip calorimetry (FSC) studies using cooling rates from 60 to 13,800 °C min^?1 revealed that the formation of β‐crystals significantly depended on the cooling rates. At cooling rates below 3000 °C min^?1, only β‐crystals existed. However, at cooling rates above 6000 °C min^?1, β‐crystals failed to form. Moreover, a lower critical crystallization temperature that corresponded to the generation of β‐crystals was investigated using cooling‐induced crystallization, and the results are in good agreement with those of a previous study. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43767.     

A novel highly efficient β‐nucleating agent for isotactic polypropylene

A novel highly efficient β‐nucleating agent for isotactic polypropylene (iPP), hexahydrophthalic barium (HHPA‐Ba), was found and its effects on the mechanical properties, the β‐phase content, and crystallization behavior of iPP were investigated, respectively. The results show that the β‐phase content of nucleated iPP (k_β value) can reach 80.2% with 0.4 wt % HHPA‐Ba. The impact strength and crystallization peak temperature of nucleated iPP are greatly increased. Compared with pure iPP, the impact strength of nucleated iPP can increase 2.4 times. Meanwhile, the spherulite size of nucleated iPP is dramatically decreased than that of pure iPP. The Caze method was used to investigate the nonisothermal crystallization kinetics of nucleated iPP and the crystallization active energy was achieved by Kissinger method. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Effect of polystyrenes with different architectures on the β‐nucleating efficiency and toughening of isotactic polypropylene

The effect of polystyrenes (PSs) with different architectures (three‐arm star‐shaped polystyrene (sPS), comb‐like branched polystyrene (cPS) and linear polystyrene) on their β‐nucleating efficiency for isotactic polypropylene (iPP) during crystallization and final impact and the tensile properties of iPP/PS blends were investigated by dynamic rheological measurements, SEM, DSC, polarized optical microscopy, wide angle X‐ray diffraction and mechanical property measurements. The results show that the architecture of PS has marked influence on its dispersibility in iPP and β‐nucleating efficiency. For iPP/cPS blend, plenty of short side chains reduce the probability of cPS chain entanglements, facilitating the interdiffusion between iPP and cPS chains. A favorable interfacial interaction results in good dispersibility, high β nucleating efficiency and an excellent toughening effect of cPS on iPP. However, the relatively high chain entanglement degree of sPS may not be in favor of chain diffusion between iPP and sPS and therefore relatively poor dispersibility and toughening effect are obtained. The elongation at break and impact strength of iPP were dramatically improved, especially with the addition of 1 wt% cPS. The toughening mechanism of PS on iPP is the dissipated energy caused by cavitation and the β‐nucleating effect of PS. © 2018 Society of Chemical Industry     

Study of phenyl‐terminated hyperbranched polyester as a special β‐nucleating agent on the toughness of isotactic polypropylene

The effect of phenyl‐terminated hyperbranched polyester (HBP‐Bz) with different generation (the first generation and the fourth generation) as a special β‐nucleating agent on the toughness of isotactic polypropylene (iPP) was investigated by dynamic rheological measurements, scanning electron microscopy, differential scanning calorimetry, wide‐angle X‐ray diffraction, polarized optical microscopy, and mechanical properties measurements. The results show that the β nucleating activity of HBP‐Bz significantly depends on its concentration and molecular structure. The relative content of β‐crystal form (K_β) increases with the increasing HBP‐Bz percentage reaches a maximum and then decreases as HBP‐Bz percentage further increases. The K_β values of iPP/HBP‐G1‐1% and iPP/HBP‐G4‐1% blends are 26.52% and 20.80%, respectively. When compared with HBP‐G4, HBP‐G1 has incompact molecular structure, facilitating the π–π interaction between phenyl‐terminated groups and the helix chains of iPP crystallize on it, and therefore relatively good dispersibility, high β nucleating activity and excellent toughening effect are obtained. The impact strength of iPP was dramatically improved, especially with addition of 1 wt% HBP‐G1. POLYM. ENG. SCI., 59:E133–E143, 2019. © 2018 Society of Plastics Engineers     

Isotactic polypropylene toughened with poly(acrylonitrile–butadiene–styrene): Compatibilizing role of maleic anhydride grafted polypropylene

The β‐nucleating activity and toughening effect of acrylonitrile–butadiene–styrene (ABS) graft copolymer on isotactic polypropylene (iPP) and the compatibilizing role of maleic anhydride grafted polypropylene (PP‐g‐MAH) on the iPP/ABS blends were investigated. The results show that ABS can induce the formation of β‐crystal in iPP, and its β‐nucleating efficiency depends on its concentration and dispersibility. The relative content of β‐crystal form is up to 36.19% with the addition of 2% ABS. The tensile and impact properties of the iPP were dramatically enhanced by introducing ABS. The incorporation of PP‐g‐MAH into the iPP/ABS blends inhibits the formation of β‐crystal. The crystallization peaks of the blends shift toward higher temperature, due to the heterogeneous nucleation effect of PP‐g‐MAH on iPP. The toughness of iPP/ABS blends improved due to favorable interfacial interaction resulting from the compatibilization of PP‐g‐MAH is significantly better than the β‐crystal toughening effect induced by ABS. POLYM. ENG. SCI., 59:E317–E326, 2019. © 2019 Society of Plastics Engineers     

Different β nucleants and the resultant microstructural,fracture, and tensile properties for filled and unfilled ISO polypropylene

This article explores the use of two β nucleants to improve the fracture behavior of filled and unfilled homo‐polypropylene (PP). The first was based upon an organic quinacridone, whereas the second was based upon the inorganic calcium pimelate. Formulations containing various concentrations of nucleant were prepared using single screw extrusion and then characterized by X‐ray diffraction, differential scanning calorimetry (DSC), Izod impact strength, and tensile testing. The quinacridone nucleating agent produced higher levels of β crystallinity and better improvement in strain to failure, whereas the calcium pimelate imparted greater improvement in impact strength regardless of whether the PP was filled or unfilled. No direct relationship between β crystallinity and fracture properties was observed though synergistic enhancement in impact strength was evident. By varying the concentration of calcium carbonate in the calcium pimelate from 10 : 1, 5 : 1, 2 : 1, and 1 : 1 weight composition of calcium carbonate to pimelic acid, similar property enhancements were achieved regardless of composition although the 10 : 1 sample did produce superior elongation to break. The importance of cooling rate on microstructure within each sample was explored via a through the thickness study using DSC and nano‐indenting methods. Variations in the β content through the thickness were related to cooling and found to be independent of sample composition and processing. Elastic properties varied inversely with β content. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Improved conductivity and thermal stability by the formation of a charge‐transfer complex in β‐nucleation‐agent‐nucleated and MWCNT‐filled iPP composites

In this study, the influence of β‐nucleation agent (β‐NA) on the morphology and properties of multi‐walled carbon nanotube (MWCNT) filled isotactic polypropylene (iPP) composites was explored in details. The results show that the incorporation of β‐NA has promoted the dispersion of MWCNT in the iPP matrix, which is profitable for improving the thermal stability and conductivity properties of MWCNT‐iPP composites. Besides, the 0.05 wt % β‐NA nucleated samples exhibit higher impact toughness than that of un‐β‐NA‐nucleated ones. Further SEM observations show that the morphology of MWCNT changes from large agglomerations to small clusters with doping of β‐NA. The main reason is that the incorporation of β‐NA (TMB‐5) in MWCNT filled iPP matrix has led to the formation of a charge‐transfer complex. Some of these clusters act as nucleation sites for inducing crystallization of α spherulites, which have a compete growth with β‐NA induced β crystals. Meanwhile, other clusters exist in the inter‐lamella amorphous phase of β crystals, some of them even combine two adjacent β spherulites. Accordingly, a large conductive network comes into being. Based on the investigated results, a mechanism model is proposed. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Crystalline morphology and mechanical properties of isotactic polypropylene composites filled by wollastonite with β‐nucleating surface

Wollastonite‐filled α‐isotactic polypropylene (iPP) and β‐iPP were prepared through introduction of wollastonite (W) and wollastonite with β‐nucleating surface (W_x) in iPP matrix. The α‐ and β‐nucleating ability of wollastonite, crystalline morphology, and mechanical properties of injected iPP filled by wollastonite with different nucleating surface were compared using differential scanning calorimetry, wide‐angle X‐ray diffraction, polarizing optical microscopy, mechanical testing, and scanning electron microscopy. The results indicated that iPP filled by wollastonite with different nucleating surface has different crystalline morphology, melting behavior, and mechanical properties. The W and W_x filled iPP mainly formed α‐ and β‐phase iPP, respectively. The tensile and flexural modulus of iPP/W and iPP/W_x increased with increasing wollastonite content, and the tensile and flexural modulus of iPP/W_x were lower than that of iPP/W. The tensile property, flexural property, and impact strength of iPP/W_x were higher than that of iPP/W and β‐iPP. The synergistic effect of reinforcing of wollastonite and toughening of β‐phase leads to higher mechanical properties. POLYM. COMPOS., 35:1445–1452, 2014. © 2013 Society of Plastics Engineers     

Effect of N,N′‐diphenyl adipamide on the formation of the β‐crystalline form in isotactic polypropylene

The polymorphic compositions and mechanical properties of isotactic polypropylene (iPP) samples nucleated by a selective β‐nucleating agent [N,N′‐diphenyl adipamide (DPA)] were investigated with wide‐angle X‐ray diffraction, polarized light microscopy, scanning electron microscopy, and mechanical tests. It was found that β‐phase crystals emerged with the addition of DPA, and the relative proportion of the β‐crystalline form reached the maximum value of 0.97 with the addition of 0.1 wt % DPA. The curved lamellae in the β spherulites were like flowers. The β spherulites were etched more easily than α spherulites because amorphous regions were distributed inside the β spherulites. The Izod notched impact strength increased sharply with the addition of DPA and attained the maximum value of 7.30 kJ/m² (the value of blank iPP was 3.13 kJ/m²) with the addition of 0.1 wt % DPA. An analysis of the misfit factors between DPA and β‐iPP showed that β‐iPP could epitaxially crystallize on the DPA crystal well. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Simultaneously improving tensile strength and toughness of melt‐spun β‐nucleated isotactic polypropylene fibers

Polymer processing methods generally play a crucial role in determining the development of microstructure in the fabricated product. In this study, isotactic polypropylene (iPP) melt containing 0.05 wt % β‐nucleating agent (β‐NA) was extruded via a melt flow rate indicator. The molten extrudate was stretched into a fiber upon various take‐up velocities (TVs). The microstructures of the fiber were investigated by differential scanning calorimeter, two‐dimensional wide‐angle X‐ray diffraction, and small‐angle X‐ray scattering. Also, its tensile properties (including tensile strength, modulus, elongation at break, and toughness) were measured by tensile test. Interestingly, the tensile strength (135.0 MPa) of a melt‐spun β‐nucleated iPP fiber fabricated at 400 cm/min was enhanced by 115.2%, compared with that (62.7 MPa) prepared at 100 cm/min, with a considerable increment in toughness (from 661 to 853 MJ/m³). The enhancement mechanism for tensile properties was discussed based on the microstructures. This work offers a simple approach to prepare β‐nucleated iPP fibers with excellent strength and toughness. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43454.     

Variation of non‐isothermal crystallization behavior of isotactic polypropylene with varying β‐nucleating agent content

The non‐isothermal crystallization behavior, the crystallization kinetics, the crystallization activation energy and the morphology of isotactic polypropylene (iPP) with varying content of β‐nucleating agent were investigated using differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). The DSC results showed that the Avrami equation modified by Jeziorny and a method developed by Mo and co‐workers could be successfully used to describe the non‐isothermal crystallization process of the nucleated iPPs. The values of n showed that the non‐isothermal crystallization of α‐ and β‐nucleated iPPs corresponded to a tridimensional growth with homogeneous and heterogeneous nucleation, respectively. The values of crystallization rate constant showed that the rate of crystallization decreased for iPPs with the addition of β‐nucleating agent. The crystallization activation energy increased with a small amount (less than 0.1 wt%) of β‐nucleating agent and decreased with higher concentration (more than 0.1 wt%). The changes of crystallization rate, crystallization time and crystallization activation energy of iPPs with varying contents of β‐nucleating agent were mainly determined by the ratio of the content of α‐ and β‐phase in iPP (α‐PP and β‐PP) from the DSC investigation, and the large size and many intercrossing lamellae between boundaries of β‐spherulites for iPPs with small amounts of β‐nucleating agent and the small size and few intercrossing bands among the boundaries of β‐spherulites for iPPs with large amounts of β‐nucleating agent from the SEM examination. Copyright © 2010 Society of Chemical Industry     

Effect of phenol functionalized carbon nanotube on mechanical,dynamic mechanical,and thermal properties of isotactic polypropylene nanocomposites

In this work, multiwall carbon nanotubes (MWCNT) were functionalized with phenol and characterized by using Fourier transform infrared spectroscopy (FTIR). Isotactic polypropylene (iPP)/MWCNT composites of both the unfunctionalized and functionalized MWCNT were prepared by melt blending in a miniextruder at different loadings of nanotubes (i.e., 0.1, 0.25, 1.0, and 5.0 wt%). The tensile properties of the composites were found to increase with increase in nanotube loading with a maximum in Young's modulus being achieved at 1.0 wt% loading of phenol functionalized MWCNT. The differential scanning calorimetry (DSC) studies reveal the nucleating effect of MWCNT on the crystallization of iPP. Percentage crystallinity was found to increase on phenol functionalization of MWCNT. Results of X‐ray diffraction studies of the composites are in conformity with that of DSC studies. Dynamic mechanical studies reveal that the functionalized MWCNT causes many fold increase in the storage modulus, and the effect is pronounced in the case of functionalized MWCNT. POLYM. ENG. SCI. 2012. © 2011 Society of Plastics Engineers     

Synergistic enhancement of crystallization and mechanical performance of polypropylene random copolymer by strong shear and β‐nucleating agent

Investigation of microstructure and properties is critical for the development and application of polymer materials. Polypropylene random copolymer (PPR) and β‐nucleated PPR are widely used in water pipe production. The effect of melt shear flow on the crystalline structure and mechanical properties of PPR containing β‐nucleating agent needs in‐depth understanding. In this paper, we demonstrated the preparation of PPR and PPR containing 0.1 wt% calcium pimelate (Ca‐Pim) samples by conventional injection molding (CIM) and oscillation shear injection molding (OSIM). The multilayer structures and morphologies of the samples were characterized by SEM, two‐dimensional X‐ray scattering and DSC. The mechanical properties and the microstructures of samples prepared by these two injection molding methods were compared. Compared with samples prepared by CIM, the stronger shear provided by OSIM induced the formation of a thicker layer of a shish‐kebab structure and a higher content of γ crystals, and dramatically suppressed the β‐nucleating effect of Ca‐Pim. The OSIM samples have more shish‐kebab structures and higher crystallinities than CIM samples and therefore the former exhibit better rigidity than the latter. The β crystals in the core layer and the thicker layer of shish‐kebab structure endow OSIM‐PPR/0.1 wt% Ca‐Pim with excellent impact toughness. © 2017 Society of Chemical Industry     

Negative effect of stretching on the development of β‐phase in β‐nucleated isotactic polypropylene

On the premise that shear in the slit die of an extruder was minimized as far as possible, β‐nucleated isotactic polypropylene (iPP) was extruded. Simultaneously, once the extrudate (in the melt state) left the die exit, it was stretched at various stretching rates (SRs). For iPP with a low content of β‐nucleating agent (β‐NA), the crystallinity of β‐phase (X_β) initially increases with increasing SR, and then decreases slightly with further increase in SR. However, for iPP containing a higher content of β‐NA, with increasing SR, X_β decreases monotonically, indicating a negative effect of SR on β‐phase formation. Small‐angle X‐ray scattering and polarized optical microscopy experiments reveal that, when SR is less than 30 cm min^?1, the increasing amount of row nuclei induced by increasing SR is mainly responsible for the increase of X_β. In contrast, when SR exceeds 30 cm min^?1, the overgrowth of shish structures unexpectedly restrains the development of β‐phase, and spatial confinement is considered as a better explanation for the suppression of β‐phase. Copyright © 2011 Society of Chemical Industry